Abdominal aortic aneurysm The right clinical information, right where it's needed Last updated: Nov 13, 2017 Table of Contents Summary 3 Basics 4 Definition 4 Epidemiology 4 Aetiology 4 Pathophysiology 4 Classification 5 Prevention Screening Diagnosis 6 6 7 Case history 7 Step-by-step diagnostic approach 7 Risk factors 8 History & examination factors 10 Diagnostic tests 10 Differential diagnosis 12 Treatment 15 Step-by-step treatment approach 15 Treatment details overview 27 Treatment options 29 Emerging 35 Follow up 36 Recommendations 36 Complications 36 Prognosis 37 Guidelines 38 Diagnostic guidelines 38 Treatment guidelines 38 References 40 Images 52 Disclaimer 59 Summary ◊ Typically asymptomatic and discovered incidentally, but abdominal pain and back pain are the most common symptomatic complaints. ◊ Diagnosis relies on imaging. Ultrasound remains the definitive test for initial diagnosis and screening. CT scan is typically required for preoperative planning. ◊ Repair is deferred until the theoretical risk of rupture exceeds the estimated risk of operative mortality. Repair is indicated in patients with symptomatic AAA or asymptomatic AAA with a diameter exceeding 5.5 cm in men or 5.0 cm in women. ◊ Complications of treatment include cardiac and pulmonary events, mesenteric ischaemia, renal failure, bleeding, wound and graft infection, spinal cord ischaemia/paraplegia, embolisation/limb ischaemia, and late graft complications (i.e., aorto-enteric fistula and aortic pseudoaneurysm). Endovascular repair offers the additional potential complications of endoleak, graft occlusion, and graft migration with aortic neck expansion. Abdominal aortic aneurysm Basics BASICS Definition Abdominal aorta aneurysm (AAA) is a permanent pathological dilation of the aorta with a diameter >1.5 times the expected anteroposterior (AP) diameter of that segment, given the patient's gender and body size.[1] [2] [Fig-1] This is approximately 3 cm in most people. More than 90% of aneurysms originate below the renal arteries.[3] Epidemiology In the UK, Denmark, and Australia, using randomised controlled trials, screening for AAA was carried out. In total, there were 128,891 men and 9342 women. A Cochrane review of the data (2007) found that, between the age of 65 and 79 years, 5% to 10% of men have AAA.[8] Epidemiology varies by region and with a number of other demographic factors. The general prevalence of 2.9 cm to 4.9 cm AAAs range from 1.3% for men aged 45 to 54 years, to 12.5% for men 75 to 84 years of age (0% and 5.2% for women, respectively).[3] The prevalence of aneurysms among men increases by about 6% per decade.[7] In 2004 AAA was the 14th leading cause of death for the 60- to 85-year-old age group in the US, and there were 13,753 deaths from aortic aneurysm and dissection combined in 2004.[9] [10]Prevalence among men is 4 to 6 times higher than in women.[1] [11] Aetiology The aetiology is multi-factorial. Traditionally, arterial aneurysms were thought to arise from atherosclerotic disease, and certainly intimal atherosclerosis reliably accompanies AAA.[12] More recent data suggest that altered tissue metalloproteinases may diminish the integrity of the arterial wall.[5] The underlying pathophysiology remains constant with aortic elastic medial degeneration and mild cystic medial necrosis resulting in aortic dilation and aneurysm formation. Pathophysiology The pathogenesis is complex and multi-factorial. Histologically there is obliteration of collagen and elastin in the media and adventitia, smooth muscle cell loss with resulting tapering of the medial wall, infiltration of lymphocytes and macrophages, and neovascularisation.[12] There are 4 mechanisms relevant to AAA development:[13] • Proteolytic degradation of aortic wall connective tissue: matrix metalloproteinases (MMPs) and other proteases are derived from macrophages and aortic smooth muscle cells and secreted into the extracellular matrix. Disproportionate proteolytic enzyme activity in the aortic wall may promote deterioration of structural matrix proteins (e.g., elastin and collagen).[3] Increased expression of collagenases MMP-1 and -13 and elastases MMP-2, -9, and -12 has been demonstrated in human AAAs.[14] [15] [16] [17] • Inflammation and immune responses: an extensive transmural infiltration by macrophages and lymphocytes is present on aneurysm histology and these cells may release a cascade of cytokines that subsequently activate many proteases.[12] Additionally, deposition of IgG into the aortic wall 4 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Basics Classification Types of AAA Specific types of AAA are:[4] [5] • Congenital: while medial degeneration occurs naturally with age, it is accelerated in patients with bicuspid aortic valves and Marfan's syndrome. • Infectious: infection of the aortic wall (mycotic aneurysm) is a rare aetiology. Staphylococcus and Salmonella are the most common pathogens. Chlamydia pneumoniae has been postulated as an infectious aetiology for conventional aneurysms. • Inflammatory: the aetiology of inflammatory AAAs remains controversial. This variant is characterised by an abnormal accumulation of macrophages and cytokines in diseased tissue. Pathologically there is perianeurysmal fibrosis, thickened walls, and dense adhesions. This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 5 BASICS supports the hypothesis that AAA formation may be an autoimmune response. There is currently interest in the role of reactive oxygen species and antioxidants in AAA formation.[14] [18] [19] [20] [21] • Biomechanical wall stress: elastin levels and the elastin-collagen ratio decrease progressively distal down the aorta. Diminished elastin is associated with aortic dilation, and collagen degradation predisposes to rupture.[11] Additionally, data support increased MMP-9 expression and activity, disordered flow and an increase in wall tension, and relative tissue hypoxia in the distal aorta (i.e., infra-renal).[14] [22] [23] • Molecular genetics: while there is no single genetic defect or polymorphism responsible, there is familial clustering, a common HLA subtype, and several altered gene expressions and polymorphisms linked, suggesting a genetic role in pathogenesis.[14] [24] [25] Abdominal aortic aneurysm Prevention Screening PREVENTION Screening may reduce the incidence of aortic rupture, especially if applied to high-risk groups.[8] [60] [61] [62]Current recommendations include: [47] • One-time ultrasound screening for AAA is recommended for all men aged ≥65 years. Screening men as early as 55 years is appropriate for those with a family history of AAA. • Re-screening patients for AAA is not recommended if an initial ultrasound scan performed on patients aged ≥65 years demonstrates an aortic diameter of 2.6 cm. • Surveillance imaging at 12-month intervals is recommended for patients with an AAA of 3.5 to 4.4 cm in maximum diameter. • Surveillance imaging at 6-month intervals is recommended for those patients with an AAA between 4.5 and 5.4 cm in maximum diameter. • Follow-up imaging at 3 years is recommended for those patients with an AAA between 3.0 and 3.4 cm in maximum diameter. • Follow-up imaging at 5-year intervals is recommended for patients whose maximum aortic diameter is between 2.6 and 2.9 cm. These recommendations are based on a meta-analysis of published data regarding the use of screening programmes to detect AAA compiled and summarised by the United States Preventative Services Task Force (USPSTF), several randomised trials, and the concept that screening for AAA and surgical repair of large AAAs (≥5.5 cm) in men aged 65 to 75 years who have ever smoked leads to decreased AAA-specific mortality.[47] [49] [63] [64] [65] [66] [67] [68] [69] [70] [71] While the USPSTF argues against screening in women, some authors argue that in certain subgroups of women at increased risk of AAA (i.e., age ≥65 years with a positive history of smoking or family history of AAA) screening should be considered with one-time ultrasound.[1] [44] [47] [63] [72] 6 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Diagnosis Case history Case history #1 A 70-year-old man presents to his primary care physician for a health maintenance examination. He has been feeling well and in his usual state of good health. His medical history is notable for mild HTN and he has a 100-pack-year tobacco history. On clinical examination, there is a palpable pulsatile abdominal mass. Case history #2 A 55-year-old man with a history of HTN (well controlled with medication) and tobacco use presents to his primary care physician with a 2-day history of constant and gnawing hypogastric pain. The pain has been steadily worsening in intensity. He believes the pain radiates to his lower back and both groins at times. While he cannot identify any aggravating factors (such as movement), he feels the pain improves with his knees flexed. There is a palpable pulsatile mass just left of midline below the umbilicus. He is immediately referred for definitive management, but during transfer becomes hypotensive and unresponsive. Other presentations The triad of abdominal pain, weight loss, and elevated ESR suggests inflammatory AAA.[5] A tender, palpable pulsatile mass on examination and elevated CRP may also be present. Abdominal or back pain with fever is suggestive of mycotic or infectious AAA. Typically there is history of arterial trauma, IV drug abuse, local or concurrent infection, bacterial endocarditis, or impaired immunity. Osteomyelitis of the thoracic or lumbar spine may develop. Anaemia, leukocytosis, and positive blood cultures are common.[6] Diagnosis may be aided by complications of unruptured aneurysms, including distal embolisation, acute thrombosis, or symptoms caused by ureterohydronephrosis.[7] DIAGNOSIS Step-by-step diagnostic approach Patients most commonly lack any symptoms and their aneurysm is noted on physical examination or radiographic studies performed for other reasons. History Typical symptoms include abdominal, back, and groin pain. Medical history is directed towards risk factors: • Development (i.e., hyperlipidaemia, connective tissue disorder, COPD, and HTN)[1] [3] [7] [11] [26] [41] [42] • Expansion (i.e., previous cardiac or renal transplant, previous stroke, advanced age (>70 years), and severe cardiac disease)[44] [45] • Rupture (i.e., female sex, previous cardiac or renal transplant, HTN).[7] [43] [44] [46] This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 7 Abdominal aortic aneurysm Diagnosis A history of cigarette smoking increases a patient's risk of AAA development, expansion, and rupture.[7] [26] [27] [28] [44] A history of previous abdominal surgery or previous endovascular aortic aneurysm repair can be elicited as well as family history of AAA. Physical examination The abdomen can be palpated for a pulsatile abdominal mass and abdominal tenderness. Physical examination should include an assessment of femoral and popliteal arteries in all patients with a suspected AAA as an AAA is present in 62% of patients with a popliteal aneurysm and in 85% of patients with a femoral artery aneurysm.[44] [45] [47] Aneurysm palpation on clinical examination has only been shown to be sensitive in thin patients and those with AAA >5 cm with an overall sensitivity and specificity of 68% and 75%, respectively.[1] [48] Ruptured aneurysm presents with the triad of abdominal and/or back pain, pulsatile abdominal mass, and hypotension. The presence of fever may increase suspicion for infectious AAA in the appropriate clinical setting. Key tests Ultrasonography is the initial method of choice for AAA detection (sensitivity and specificity of 95% and nearly 100%, respectively). Once the diagnosis is made, further imaging with CT, MRI, or magnetic resonance angiography (MRA) is used for anatomical mapping to assist with operative planning (open or endovascular).[7] [49] Elevated ESR and CRP support a diagnosis of possible inflammatory AAA. Leukocytosis and a relative anaemia on FBC with positive blood cultures are indicative of infectious AAA. DIAGNOSIS Predictors of rupture risk including AAA expansion rate, increase in intraluminal thrombus thickness, wall stiffness, wall tension, and peak AAA wall stress.[47] [50] Risk factors Strong cigaret te smoking • This is the risk factor most strongly associated.[1] [7] [11] [26] [27] • Active cigarette smoking is independently associated with histological high-grade tissue inflammation.[28] • The duration of smoking is significantly associated with an increased risk in a linear dose-response relationship. Each year of smoking increases the relative risk by 4%.[27] hereditary/family history • Studies support a familial aggregation of and genetic predisposition to AAA.[1] [7] [25] [29] [30] [31] [32] [33] [34] [35] • The age- and sex-adjusted relative risk to a first-degree relative of an AAA patient is 11.6% and a history of AAA in a parent confers the same excess risk.[32] 8 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Diagnosis • The overall prevalence of AAA in siblings of AAA patients is 8 times that observed among control cohort.[33] First-degree relatives have been shown to have an AAA in 15% to 28% of cases.[3] [34] [35] increased age • Prevalence increases with age.[1] [11] • Most frequently diagnosed in men >55 years of age and rupture rarely occurs before 65 years of age. • AAA is discovered approximately 10 years later in women.[7] [36] [37] male sex (prevalence) • AAAs are 4 to 6 times more prevalent in men than women.[1] [7] [11] female sex (rupture) • Female sex increases risk of rupture.[34] [38] congenital/connective tissue disorders • Aortic degeneration is accelerated in patients with bicuspid aortic valves, Marfan's syndrome, and during pregnancy.[39] [40] [41] • Marfan's syndrome specifically is associated with cystic medial necrosis of the aorta secondary to an autosomal dominant anomaly in fibrillin type 1, a structural protein that directs and orients elastin in the developing aorta.[39] [40] As a result, the mature aorta demonstrates abnormal elastic properties, progressive stiffening, and dilation.[41] Weak hyperlipidaemia COPD • This is attributed to tobacco-induced elastin degradation.[3] [7] • Studies suggest that the association between reduced respiratory function and AAA may be due to the activation of inflammation and haemostasis in response to injury.[42] atherosclerosis (i.e., CAD, peripheral arterial occlusive disease) • CAD is an independent associated risk factor.[1] [26] HTN • HTN is a weak independent risk factor.[1] [7] [11] • There is a relation between systolic BP and AAA in women and an association with ever-use antihypertensive medication and AAA risk for both sexes.[11] [37] This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 9 DIAGNOSIS • Lipoproteins are elevated in patients with AAA independent of cardiovascular risk factors and extent of atherosclerosis.[3] [7] • AAA patients have significantly lower levels of apolipoprotein AI and HDL cholesterol than matched controls with aorto-iliac occlusive disease.[1] [3] • High serum total cholesterol is a relatively weak risk factor for AAA, whereas high HDL cholesterol was strongly associated with a low risk of AAA.[11] [37] Diagnosis Abdominal aortic aneurysm increased height • Increased height is an independent associated risk factor, although after adjustment for age and sex the association was no longer significant.[1] [26] [43] central obesity • While obesity is generally not considered a risk factor, one study of more than 12,000 men demonstrated an independent association between central obesity and AAA.[37] non-diabetic • Diabetes is negatively associated with AAA.[26] [34] [37] History & examination factors Key diagnostic factors presence of risk factors (common) • Key risk factors include cigarette smoking, family history, increased age, male sex for prevalence and female sex for rupture, and congenital/connective tissue disorders. palpable pulsatile abdominal mass (uncommon) • Aneurysm palpation on clinical examination has been shown to be sensitive only in thin patients and those with AAA >5 cm (sensitivity and specificity of 68% and 75%, respectively).[1] [48] Other diagnostic factors abdominal, back, or groin pain (uncommon) DIAGNOSIS • However, patients are usually asymptomatic and their aneurysm is detected incidentally. hypotension (uncommon) • Patients with ruptured aneurysm present with the triad of abdominal and/or back pain, pulsatile abdominal mass and hypotension. Diagnostic tests 1st test to order Test Result abdominal ultrasound aortic dilation of >1.5 times the expected anterior-posterior diameter of that segment, given the patient's sex and body size; this is approximately 3 cm in most individuals • Definitive test (sensitivity and specificity of 92% to 99% and nearly 100%, respectively).[1] [2] [48] [8] • The ultrasound is performed perpendicular to the aortic axis as oblique views may overestimate the true aortic diameter.[2] • Intra-observer correlation may be better near the aortic bifurcation than in the proximal infrarenal aorta.[49] • Unfortunately, ultrasound offers little utility in imaging aneurysms close to the origins of, or proximal to, the renal arteries.[51] [52] 10 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Diagnosis Abdominal aortic aneurysm Other tests to consider Test Result ESR/CRP elevated • Suggests inflammatory AAA. FBC leukocytosis, anaemia • Leukocytosis and a relative anaemia on FBC with positive blood cultures are indicative of infectious AAA. blood cultures positive • Leukocytosis and a relative anaemia on FBC with positive blood cultures are indicative of infectious AAA. CT • May demonstrate blood within the thrombus (crescent sign), low thrombus-to-lumen ratio retroperitoneal haematoma, discontinuity of the aortic wall, or extravasation of contrast into the peritoneal cavity, which are all signs of impending rupture.[7] [53] • Also useful in diagnosing aortic aneurysms close to the origins of, or proximal to, the renal arteries.[52] [53] MRI/MRA • Preoperative study of choice for operative strategy if a patient has an iodinated contrast allergy. aortography • Adjunctive modality for preoperative planning. aaortic dilation of >1.5 times the expected anterior-posterior diameter of that segment, given the patient's sex and body size; this is approximately 3 cm in most individuals aortic dilation of >1.5 times the expected anterior-posterior diameter of that segment, given the patient's sex and body size; this is approximately 3 cm in most people This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 11 DIAGNOSIS Contrast aortography may aid with preoperative planning and sizing for those patients unable to undergo CT imaging. Additionally, it may be used to diagnose and treat arterial occlusive disease prior to open AAA repair or endovascular repair (EVAR) (i.e., renal or mesenteric disease) Diagnosis Abdominal aortic aneurysm Differential diagnosis Condition Diverticulitis Renal colic DIAGNOSIS Irritable bowel syndrome (IBS) 12 Differentiating signs / Differentiating tests symptoms • Obstipation; abdominal pain is more common and typically localises to the left lower quadrant. • No pulsatile abdominal mass on clinical examination. Instead, abdominal or perirectal "fullness" may be appreciated. Fever is possible.[54] • • Severe abdominal pain that starts in the flank and radiates anteriorly to the groin. • Associated with nausea, emesis, haematuria, dysuria, and urinary frequency or urgency.[55] • • Intermittent abdominal discomfort with flares lasting 2 to 4 days. • Associated symptoms may include bloating, stool frequency, and abnormal defecation. • Women aged 20 to 40 years are affected more often than men. • On examination, most patients appear anxious, although general examination is usually normal. There may be poorly localised abdominal tenderness to palpation.[56] • • • • Stool guaiac testing may be trace positive. Leukocytosis may be present. CT scan will demonstrate a normal-calibre aorta and possibly diverticula, inflammation of the pericolic fat or other tissues, bowelwall thickness >4 mm, or a peridiverticular abscess.[54] Urinalysis positive for blood and may demonstrate crystals and/or evidence of infection. Ultrasound and CT scan will demonstrate a normalcalibre aorta and possibly ureteral or renal stones.[55] Imaging modalities are often inconclusive, but will demonstrate a normalcalibre aorta. This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Diagnosis Abdominal aortic aneurysm Condition Inflammatory bowel disease Differentiating signs / Differentiating tests symptoms • Abdominal pain is often "crampy" and left-sided. Patients typically suffer from diarrhoea (bloody and non-bloody), urgency of defecation, and tenesmus. • Extra-intestinal manifestations are common in Crohn's disease. • Abdominal examination may demonstrate abnormal bowel sounds, detection of an abdominal mass, and pain on palpation. Mucocutaneous lesions may be visible. Peri-anal fistulae, fissures, or abscesses may be present on rectal examination.[57] • • • Pain is typically periumbilical with localisation to the right lower quadrant. • Associated nausea, emesis, and anorexia are common. • Patients are classically febrile with tenderness in the right lower quadrant or rebound tenderness on abdominal examination. • Ovarian torsion • Women suffer sudden, continuous, non-specific pain in the lower abdomen; nausea and emesis are common. Patients may demonstrate fever on clinical examination and an adnexal mass may be palpable.[58] • Leukocytosis may be present. Ultrasound will demonstrate a normal calibre aorta and possible reduced or absence of adnexal vascular flow.[58] GI haemorrhage • Patients presenting with haemorrhagic shock may mimic aortic rupture. A history of previous GI bleed, haematemesis, melaena, or bright red blood per rectum is common. • Historical risk factors for GI malignancy or peptic ulcer disease may be elicited. • On rectal examination gross blood may be visible or coffee ground haematemesis may be returned with nasogastric tube placement. • Stool is likely to be guaiac positive. Endoscopic evaluation may demonstrate the luminal bleeding source along with mucosal ulcerations, polyps, or tumour. Radiographical imaging with ultrasound or CT scan will demonstrate a normal calibre aorta. Appendicitis • • • Leukocytosis and sterile pyuria on urinalysis is common. Imaging with ultrasound or CT scan will demonstrate a normal-calibre aorta with an inflamed appendix or evidence of perforation. This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 13 DIAGNOSIS • Anaemia is common. Radiographical imaging (i.e., ultrasound or CT scan) will demonstrate a normalcalibre aorta. Endoscopic evaluation with biopsy shows typical lesions of ulcerative colitis or Crohn's disease.[57] Diagnosis Abdominal aortic aneurysm Condition • Acute embolic or thrombotic occlusion of the splanchnic vessels results in a marked disparity between acute excruciating mid-abdominal pain and a paucity of early physical findings. • Patients typically suffer unremitting, intense midabdominal pain with nausea and vomiting that might be accompanied by explosive diarrhoea. • Most splanchnic artery aneurysms are asymptomatic until rupture.[59] • • • Leukocytosis, haemoconcentration, and systemic acidosis are common with acute splanchnic vessel occlusion. Elevated levels of serum amylase, inorganic phosphorous, creatinine phosphokinase, and alkaline phosphatase may accompany frank bowel infarction. Angiography is diagnostic and potentially therapeutic in the case of vascular occlusion. Ultrasound and CT scan will demonstrate a normalcalibre aorta and will diagnose any splanchnic artery aneurysms.[59] DIAGNOSIS Splanchnic artery aneurysms/acute occlusion Differentiating signs / Differentiating tests symptoms 14 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Treatment Step-by-step treatment approach Patients presenting with a ruptured aneurysm require emergent repair, and for patients with symptomatic aortic aneurysms, repair is indicated regardless of diameter.[73] For AAA detected as an incidental finding, repair is deferred until the theoretical risk of rupture exceeds the estimated risk of operative mortality. Generally, repair is indicated in patients with large asymptomatic AAA (e.g., with a diameter exceeding 5.5 cm in men or 5.0 cm in women, in the US), although treatment decisions based on greater size may differ in other countries (e.g., UK).[1] [74] [75] [76] [77] [78] Types of repair Open repair: • The conventional open repair ensues through a retroperitoneal (RP) or transperitoneal incision. With proximal and distal aortic control obtained, the aneurysm is opened, back-bleeding branch arteries are ligated, and a prosthetic graft is sutured from normal proximal aorta to normal distal aorta (or iliac segments). Once flow is restored to the bilateral iliac arteries the aneurysm sac is closed over the graft.[79] • Although advocates of an RP approach claim various physiological benefits, including reductions in fluid losses, cardiac stress, postoperative pulmonary complications, and severity of ileus, randomised prospective studies have generated conflicting results. A retroperitoneal approach should be considered for patients in which aneurysmal disease extends to the juxtarenal and/or visceral aortic segment, or in the presence of an inflammatory aneurysm, horseshoe kidney, or hostile abdomen.[47] [80] [81] • Straight tube grafts are recommended for repair in the absence of significant disease of the iliac arteries.[47] • The proximal aortic anastomosis should be performed as close to the renal arteries as possible.[47] It is recommended that all portions of an aortic graft should be excluded from direct contact with the intestinal contents of the peritoneal cavity.[47] • Re-implantation of a patent inferior mesenteric artery (IMA) should be considered under circumstances that suggest an increased risk of colonic ischaemia (i.e., associated coeliac or superior mesenteric artery occlusive disease, an enlarged meandering mesenteric artery, a history of prior colon resection, inability to preserve hypogastric perfusion, substantial blood loss or intraoperative hypotension, poor IMA backbleeding when graft open, poor Doppler flow in colonic vessels, or should the colon appear ischaemic).[47] [82] • This repair is effective and durable; 5-year survival rates after intact aneurysm repair average 60% to 75%.[83] • Complications include cardiac and pulmonary events, mesenteric ischaemia, renal failure, bleeding, wound and graft infection, spinal cord ischaemia/paraplegia, embolisation/limb ischaemia, and late graft complications (i.e., aorto-enteric fistula and aortic pseudoaneurysm).[1] [84] • The operative mortality associated with open repair averages 2% to 7%; this has prompted a movement towards less-invasive technique and endovascular AAA repair.[85] [86] • EVAR is progressively replacing open repair for the treatment of infrarenal AAA, and now accounts for more than 50% of all AAA repairs in the US.[47] This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 15 TREATMENT Endovascular repair (EVAR): Abdominal aortic aneurysm Treatment • Data suggest that in patients with large AAAs (ranging from 5 to 5.5 cm) undergoing elective repair, EVAR is equivalent to open repair in terms of overall survival, although the rate of secondary interventions is higher for EVAR.[87] [88]EVAR also reduces AAA-related mortality (but not longerterm overall survival) in patients unsuitable for open repair.[89] • EVAR involves the transfemoral endoluminal delivery of a covered stent graft into the aorta, thus sealing off the aneurysm wall from systemic pressures, preventing rupture, and allowing for sac shrinkage. [Fig-2] [Fig-3] • Additional complications may include endoleak, graft occlusion, and graft migration with aortic neck expansion.[83] • Studies support that EVAR offers patients an early perioperative mortality benefit (0% to 1.7%) with decreased hospital length of stay and blood product utilisation.[1] [90] [91] [92]The advantage is lost with longer follow-up, and no advantage with respect to all-cause mortality or quality of life has been demonstrated.[1] [93] [94] [95] [96] [97] • Late re-interventions related to AAA are more common after EVAR but are balanced by an increase in laparotomy-related re-interventions (i.e., incisional hernia repair) and hospitalisations after open surgery.[98] • Multivariate meta-regression analysis showed that rates of operative mortality, postoperative rupture, and total number of endoleaks have all fallen significantly, demonstrating a low mortality and a gradual reduction in vascular morbidity and mortality associated with endovascular repair since it was first introduced.[99] • As an adjunct to EVAR, bilateral hypogastric artery occlusion may be acceptable in certain anatomical situations for patients at high risk for open surgical repair. Buttock claudication and erectile dysfunction may occur in up to 40% of patients after unilateral embolisation - these symptoms may persist in 11% to 13% of patients following bilateral occlusion.[47] [100] [101] Internal iliac artery revascularisation techniques, involving specialised iliac branch devices, have high technical success rates and are associated with low morbidity (e.g., buttock claudication rate of 4.1%).[102] TREATMENT Treatment of co-existing cardiac disease While a substantial number of patients suffering from AAA also have underlying coronary artery disease, non-invasive stress testing should be considered for patients with a history of ≥3 clinical risk factors (i.e., CAD, congestive heart failure, stroke, diabetes mellitus, chronic renal insufficiency) and an unknown or poor functional capacity (MET <4) that are undergoing endovascular repair (EVAR) or open surgical repair, if it will change management. While routine coronary revascularisation by coronary artery bypass grafting (CABG) or percutaneous transluminal coronary angioplasty (PTCA) prior to elective vascular surgery in patients with stable cardiac symptoms does not appear to significantly alter the risk of postoperative MI or death or long-term outcome, coronary revascularisation is indicated for those patients who present with acute ST elevation MI, unstable angina, or stable angina with left main coronary artery or 3-vessel disease, as well as those patients with 2-vessel disease that includes the proximal left anterior descending artery and either ischaemia on non-invasive testing or an ejection fraction <0.5.[47] Perioperative management Regarding blood transfusion:[47] 16 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Treatment • Preoperative autologous blood donation may be beneficial for patients undergoing open aneurysm repair. • Cell salvage or an ultrafiltration device is recommended if large blood loss is anticipated or the risk of disease transmission from banked blood is considered high. • Intraoperative blood transfusion is recommended for a haematocrit <30% in the presence of ongoing blood loss. • If the intraoperative haematocrit is <30% and blood loss is ongoing, consider use of FFP and platelets in a ratio with packed blood cells of 1:1:1. Pulmonary artery catheters should not be used routinely in aortic surgery, unless there is a high risk for a major haemodynamic disturbance.[47] Central venous access is recommended for all patients undergoing open aneurysm repair.[47] DVT prophylaxis consisting of intermittent pneumatic compression and early ambulation are recommended for all patients undergoing open repair or EVAR.[47] [103] Preoperative cardiovascular risk reduction: • Preoperative beta-blockade may be reasonable in patients with intermediate- or high-risk myocardial ischaemia, and those with 3 or more RCRI (revised cardiac risk index) risk factors (e.g., diabetes mellitus, heart failure, CAD, renal insufficiency, stroke). When indicated, betablocker therapy should be started more than 1 day before surgery.[104] [105] A systematic review found that perioperative beta-blockade started within 1 day or less before non-cardiac surgery prevented non-fatal myocardial infarction, but increased the risk of stroke, death, hypotension, and bradycardia.[105] • Perioperative statin use reduces cardiovascular events during non-cardiac surgery.[104] • A large, multi-centre study of patients undergoing non-cardiac surgery found that clonidine did not reduce the rate of death or non-fatal myocardial infarction.[106] Alpha-2 agonists are not, therefore, recommended for non-cardiac surgery patients.[104] Antibiotic cover: • Antibiotic therapy is indicated for patients undergoing elective and emergent repair of ruptured AAA to cover gram-positive and gram-negative organisms (i.e., Staphylococcus aureus , Staphylococcus epidermidis , and enteric gram-negative bacilli) and prevent graft infection. • Broad-spectrum antibiotic coverage is tailored to patient clinical presentation and cultures, and in accordance with local protocols. Ruptured AAA Patients with the triad of abdominal and/or back pain, pulsatile abdominal mass, and hypotension warrant immediate resuscitation and surgical evaluation as repair offers the only potential cure.[47] [107] However, most patients with rupture will not survive to reach theatre. Overall mortality is about 90%;[83]mortality in those that reach the operating suite is 50%.[47] [Fig-4] This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 17 TREATMENT EVAR is the most efficacious method for repair, aortoiliac anatomy permitting; otherwise, traditional open repair is performed.[1] [108] [109] [110] [111] [112] [113]Operative mortality for open repair is 48%.[114]Despite frequent prolonged ICU and hospital lengths of stay, around 60% survive with long-term survival similar to that of the general population. Data support cost effectiveness.[114] [115] [116] Abdominal aortic aneurysm Treatment Supportive treatment of ruptured AAA Standard resuscitation measures are initiated immediately. This includes: • • • • • • Airway management (supplemental oxygen or endotracheal intubation) Intravenous access (central venous catheter) Arterial catheter Notify anaesthetic, ICU, and operating teams Urinary catheter Hypotensive resuscitation: aggressive fluid replacement may cause dilutional and hypothermic coagulopathy and secondary clot disruption from increased blood flow, increased perfusion pressure, and decreased blood viscosity thereby exacerbating bleeding.[108] [112] [117] [118] Infusing more than 3.5 litres of fluid preoperatively may increase the relative risk of death.[108] A target systolic BP of 50 to 70 mmHg and withholding fluids is advocated preoperatively.[112] [117] [118] • Blood product (packed red cells, platelets, and fresh frozen plasma) availability and transfusion for resuscitation, severe anaemia, and coagulopathy. Symptomatic but not ruptured AAA In patients with symptomatic aortic aneurysms, repair is indicated regardless of diameter.[73] The development of new or worsening pain may herald aneurysm expansion and impending rupture. Repair is undertaken within 24 hours; comorbid diseases are medically optimised.[1] [47] Incidental finding of small AAA For AAA detected as an incidental finding, repair is deferred until the theoretical risk of rupture exceeds the estimated risk of operative mortality. Generally, repair is indicated in patients with large asymptomatic AAA (e.g., with a diameter exceeding 5.5 cm in men or 5.0 cm in women in the US), although treatment decisions based on greater size may differ in other countries (e.g., UK).[1] [74] [75] [76] [77] [78] Current evidence and guidelines suggest that surveillance with selective repair is most appropriate for older male patients with significant comorbidities. Young, healthy patients, and especially women, with AAA between 5.0 and 5.4 cm may benefit from early repair.[47] [74] [75] [76] [77] [119] TREATMENT • While long-term survival was equivalent in the United Kingdom Small Aneurysm Trial (UKSAT) and the Aneurysm Detection and Management (ADAM) trial for both immediate surgery and surveillance groups, a trend towards a beneficial effect of early surgery was observed in both studies in the younger patient and for those with larger aneurysms[47] [75] [76] [77] [78] • The observation that EVAR is associated with reduced perioperative mortality prompted the Comparison of surveillance versus endografting for small aneurysm repair (CAESAR) and Positive impact of endovascular options for treating aneurysm early (PIVOTAL) trials in an effort to compare immediate EVAR with surveillance and selective EVAR, but neither trial has been designed to determine whether immediate EVAR might be beneficial or harmful for specific AAA size ranges or age subgroups.[47] [120] Additionally, elective repair should be considered for patients that present with a saccular aneurysm.[47] Medical goals for asymptomatic small aneurysms include: 1. Surveillance: 18 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Treatment • Infra-/juxtarenal AAAs measuring 4.0 to 5.4 cm in diameter with ultrasonography (USS)/CT should be monitored every 6 to 12 months.[73] • AAAs <4.0 cm require USS every 2 to 3 years.[73] • Expansion rates should be considered, as some advocate that expansion of 4 to 8 mm over 12 months suggests instability.[1] 2. Control modifiable risk factors for expansion and rupture: • Smoking cessation - nicotine-replacement therapy, nortriptyline, and bupropion, or counselling.[1] [7] [11] [26] [27] [121] [122] [123] • Beta-blockers may be used to reduce the rate of aneurysm expansion,[47] [124] [125] [126] although clinical trials have not supported this. 3. Aggressively manage other cardiovascular disease. • Other modifiable cardiovascular risk factors (such as hyperlipidaemia) can be treated, and statins may be considered to reduce the risk of AAA enlargement.[47] Incidental finding of large AAA Generally, repair is indicated in patients with large asymptomatic AAA (e.g., with a diameter exceeding 5.5 cm in men or 5.0 cm in women in the US), although treatment decisions based on greater size may differ in other countries (e.g., UK). Repair of aneurysms ≥5.5 cm offers a survival advantage.[1] [75] [76] [77] [78] Elective repair should be also considered for patients that present with a saccular aneurysm.[47] Data suggest that in patients with large AAAs (ranging from 5 to 5.5 cm) undergoing elective repair, EVAR is equivalent to open repair in terms of overall survival, although the rate of secondary interventions is higher for EVAR.[87] [88] EVAR also reduces AAA-related mortality (but not longer-term overall survival) in patients unsuitable for open repair.[89] Elective repair in asymptomatic patients allows for preoperative assessment, cardiac risk stratification, and medical optimisation of other comorbidities. CAD remains the leading cause of early and late mortality after AAA repair. Preoperative beta-blockade may be reasonable in patients with intermediateor high-risk myocardial ischaemia, and those with 3 or more RCRI (revised cardiac risk index) risk factors (e.g., diabetes mellitus, heart failure, CAD, renal insufficiency, stroke). When indicated, beta-blocker therapy should be started more than 1 day before surgery.[104] [105] American College of Cardiology/American Heart Association Practice Guidelines (compilation of 2005 and 2011 guideline recommendations) state: "open or endovascular repair of infrarenal AAAs is indicated in patients who are good surgical candidates… open aneurysm repair is reasonable to perform in patients who cannot comply with the periodic long-term surveillance required after endovascular repair."[73] EVAR leak Endoleak is persistent blood flow outside the graft and within the aneurysm sac.[127] [128] Type I: This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 19 TREATMENT Risk of endoleak following EVAR is 24%.[127] Endoleak is not a complication following open repair. There are 5 types of endoleak. Abdominal aortic aneurysm Treatment • Leak at the attachment site (proximal/distal end of the endograft or iliac occluder); usually immediate, but delayed leaks may occur. [Fig-5] • Repair is indicated upon discovery (endovascular extension grafts or conversion to open repair if necessary).[47] [Fig-6] [Fig-7] Type II: • Patent branch leak. [Fig-8] • Spontaneous resolution may occur, although persistence may result in sac growth.[129] • If a type II endoleak or other abnormality of concern is observed on contrast-enhanced CT imaging at 1 month after EVAR, postoperative imaging at 6 months is recommended.[47] • Treatment remains controversial and is advocated either if persistent at 6 to 12 months or when aneurysm sac size increases.[130] [131] [132] [133] • Treatment of choice is transarterial coil embolisation, although laparoscopic ligation of collateral branches, direct percutaneous translumbar puncture of the sac, translumbar embolisation, and transcatheter transcaval embolisation have been reported.[128] [130] [131] [132] [134] [135] [136] [137] Type III: • Graft defect with leak through fabric tears, graft disconnection, or disintegration of the fabric.[127] [128] • Repair is indicated upon discovery (endovascular stent graft extension).[131] [47] Type IV: • Leak from graft wall porosity.[127] [128] • These leaks are uncommon with newer stent grafts and are self-limited.[47] [131] Type V: TREATMENT • Endotension is increased intrasac pressure after EVAR without visualised endoleak on delayed contrast CT scans. • There is no standardised method to measure endotension or consensus on indicated therapy in the absence of aneurysm enlargement; however, treatment of endotension to prevent aneurysm rupture is suggested in selected patients with continued aneurysm expansion. [47] [128] Bag-valvemask ventilation animated demonstration Equipment needed • • • • • 20 Personal protective equipment, including gloves Bag-valve-mask apparatus Oxygen Reservoir bag attached to the bag-valve-mask apparatus Suction This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Treatment • Oropharyngeal airway (have available to use if needed) • Nasopharyngeal airway (have available to use if needed) • Resuscitation kit. Contraindications Complete upper airway obstruction is an absolute contraindication for bag-valve-mask ventilation. If there is suspicion of a cervical spine injury, airway opening should ideally be achieved by jaw thrust or chin lift rather than head tilt, while maintaining manual inline stabilisation (MILS). If the airway remains obstructed despite these measures, perform a head tilt using small increments until the airway is open, while maintaining MILS.[138] When it is clear from the outset that the patient needs a definitive airway (e.g., in the unconscious patient with a severe head and facial injury) call for help early while maintaining a patent airway by simple means until skilled help arrives. Consider the level of the airway obstruction. Laryngospasm due to anaphylaxis, an inhalation burn, near drowning, or a foreign body will not improve significantly with simple airway manoeuvres, and the patient may need intubation or advanced airway procedure. Indications • Respiratory failure • Failed intubation. Complications • • • • Aspiration Hypoventilation Hyperventilation Cervical spine injury. Any significant leak will cause hypoventilation of the airway and can cause gas to be forced into the stomach, heightening the risk of aspiration. Aftercare Continue to resuscitate the patient in keeping with life support guidelines, using ABCDE principles. Send for assistance as soon as possible. If resuscitation is successful and the patient regains control of their own airway, this should be regularly reassessed. Measure arterial blood oxygen saturation as soon as practical by arterial blood gas sampling and/or pulse oximetry and titrate inspired oxygen to maintain a blood arterial oxygen saturation in the range of 94% to 98%.[138] Central venous catheter insertion animated demonstration Ultrasound-guided insertion of a non-tunnelled central venous catheter (CVC) into the right internal jugular vein using the Seldinger insertion technique. This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 21 TREATMENT If the resuscitation continues or the patient’s Glasgow Coma Scale is less than 8, consider insertion of an endotracheal tube. Abdominal aortic aneurysm Treatment Equipment needed • Ultrasound appliance, with sterile probe cover and sterile transducer gel • CVC pack containing CVC and screw caps, guidewire, introducer, scalpel blade, cannulation needle, and syringe • Antiseptic preparation plus swabs for skin preparation or pre-packaged skin preparation device • Sterile gloves, sterile gown, and eye protection • Local anaesthetic (e.g., 1% or 2% lignocaine) drawn up in syringe, with 23-gauge blue and 25-gauge orange needles • Fenestrated sterile drape or occlusive transparent drape • Extra 10 mL syringes with heparin sodium solution or 0.9% saline flush • Suture and occlusive dressing • Container for the disposal of sharps. It is important to take into account the patient’s size when deciding how deeply to insert the central venous catheter. Use of an inappropriately long length of catheter may increase the risk of serious complications such as cardiac tamponade, cardiac perforation, and arrhythmias such as ventricular tachycardia, due to irritation of the endocardium.[139] [140] Contraindications Absolute contraindications: • Infection at insertion site[141] • Anatomical obstruction (thrombosis, anatomic variance, stenosis)[141] • Superior vena cava syndrome.[142] Relative contraindications: • Coagulopathy: it is generally accepted that the platelet count should be above 50 x 109/L prior to insertion of a CVC and the international normalised ratio should be below 1.5[143] • Systemic infection • Presence of pacing wires or other indwelling catheters at insertion site[141] • Right ventricular assist device • Ipsilateral pneumothorax/haemothorax.[141] Indications TREATMENT • Monitoring central venous pressure • Poor peripheral venous access or when there is a need for repeated phlebotomy • Prolonged intravenous chemotherapy and/or total parenteral nutrition, or repeated administration of blood products[144] • To deliver drugs unsuitable for peripheral infusion, such as venous sclerosants • For multiple, continuous, or incompatible infusions. Complications • Technical or equipment failure: re-attempt with assistance, possibly at an alternative site 22 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Treatment • Haemorrhage and haematoma formation: direct pressure is required to control bleeding, particularly if accidental arterial puncture has occurred • Arterial cannulation: remove needle/wire/catheter as soon as identified, and apply pressure to control haemorrhage and reduce haematoma formation • Catheter malpositioning: either cranially or extravenous. Remove catheter as soon as identified. If the catheter is positioned in the right ventricle, withdraw 5 cm or more and repeat chest radiograph • Venous air embolism: minimise the risk of air being sucked into the vein by negative intrathoracic pressures by using head-down tilt and careful technique • Venous thrombosis: higher risk with subclavian or femoral lines • Cardiac arrhythmias: withdrawing the guidewire or catheter should terminate arrhythmias caused by ventricular irritation; patients should have cardiac monitoring throughout the procedure[141] • Cardiac tamponade: this may require pericardiocentesis or surgical intervention • Carotid artery dissection: involve vascular surgeons immediately • Loss of guidewire: will require retrieval by an interventional radiologist or vascular surgeons; hold onto the guidewire with one hand at all times to avoid losing it in the patient’s vein • CVC-related sepsis: serious and potentially preventable; observe strict sterile procedure and local infection control policy • Lung injury: haemothorax, pneumothorax, and chylothorax; this should not occur when performing right internal jugular vein central line insertion, unless adopting a very low approach in the neck. Aftercare After insertion of the CVC, it is essential to confirm correct positioning before using the line for its intended purpose. This is important because ineffective positioning increases the risk of cardiac tamponade and thrombosis.[141]The optimal position of the CVC tip is a subject of ongoing debate, as no position is absolutely safe.[141] [145] Positioning the tip in the high right atrium (intracardiac placement) carries the risk of cardiac tamponade, and should be avoided,[145] although positions in the high and low superior vena cava (SVC) are also not without risk: for example, risk of thrombosis.[145] For right internal jugular vein CVC insertion it may be acceptable to aim for tip placement in the lower SVC, although this is by no means universally accepted.[145] [146] Patients with additional risk factors for thrombosis, such as those with cancer, may require different (e.g., lower) positioning of the CVC. In practice, this would be a decision to make only with senior advice.[147] Determine whether the CVC is correctly positioned using an erect chest radiograph. An erect chest radiograph is mandatory following insertion of a CVC, both to confirm the position of the tip and to check for evidence of complications such as pneumothorax and haemothorax. Therefore, the tip should ideally lie at or above the level of the carina.[141] If the catheter is in too far, the sutures/fixation can be removed and the catheter withdrawn back slightly before suturing/ fixing again. It is important to repeat the chest radiograph to reconfirm the position. However, if the This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 23 TREATMENT On the chest radiograph, the catheter should be seen to pass directly down the right side of the neck, continuing inferiorly to the right side of the mediastinum such that the tip lies at the approximate level of the carina. The carina is a radiological landmark, below which the tip is likely to be below the pericardial reflection, and therefore within the pericardial sac.[147] Abdominal aortic aneurysm Treatment catheter is too high (i.e., not deep enough) it is not advisable to advance the catheter further as you risk introducing bacteria into the circulation. A new catheter would need to be inserted, if necessary. Ensure the patient is regularly observed for signs of complications. In the days to come, signs of CVC-related sepsis should prompt immediate action in keeping with local guidance, with respect to removal of the line, culture, and antibiotic treatment. If the CVC is to be used for measurement of central venous pressure, the catheter should be correctly connected to a transducer and calibrated properly to ensure accurate readings. Female urethral catheterisation animated demonstration Equipment needed • Latex or silicone Foley catheter (14 French gauge for general use; sizes from 12 French to 24 French may be needed depending on the situation) • Sterile drape • Sterile paper towel (preferably fenestrated) • Sterile gloves • • • • • • Plastic apron Sterile pot Kidney dish 10 mL syringe filled with 10 mL sterile water (NOT saline) Lubricating anaesthetic gel (e.g., lignocaine gel) in a pre-filled 10 mL syringe Swabs and saline solution (not chlorhexidine or other cleaning solutions, as these can be irritating to the skin). Contraindications Do not perform urethral catheterisation after pelvic trauma, especially if there is a suspicion of urethral injury that may accompany a pelvic fracture, for example. In patients with a urethral injury, there is a risk that the catheter may pass straight through the urethra and into the surrounding tissues. In these patients, arrange for further imaging of the urethra before attempting catheterisation. If you fail to insert a urethral catheter on two or more occasions, seek a more experienced clinician for assistance. It may be necessary to use a curved coude tip catheter, a smaller or larger catheter, or a three-way irrigation catheter. If the patient has capacity and refuses urethral catheterisation after sufficient communication and understanding, do not perform the procedure against their wishes. Indications TREATMENT • Acute retention of urine • Perioperative urinary collection (e.g., patients undergoing abdominal surgery always need catheterisation as it is important that the bladder is fully emptied; if the bladder were full, there is a risk of it accidentally being cut during the operation) • Accurate measurement of urine output in patients who are acutely or critically unwell • Re-insertion of long-term urinary catheter • Chronic bladder obstruction and neuropathic bladder 24 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Treatment • Bladder irrigation or instillation. Patients with urinary incontinence and immobility may need catheterisation but these are not clear indications. The risk of infection must be balanced against the convenience of the catheter. Complications • Failure to catheterise:seek help from a more experienced clinician • Urinary tract infection: remove the catheter and give antibiotics as directed by local policy • Bleeding: minor bleeding is common and generally stops spontaneously; for more significant urethral haemorrhage seek expert advice from a more experienced clinician • Blocked catheter: may result from clots or other debris. Aspirating or flushing the catheter with sterile water may clear the lumen; however, repositioning may be required. If haematuria and retention of clots occurs, irrigate with a three-way catheter and contact the urology team. Aftercare Unlike catheterisation of male patients, incorrect positioning of the catheter is common in women as the urethral meatus is so close to the vaginal opening. It is very important to ensure that urine is flowing before inflating the balloon. Flowing urine is confirmation that the tip of the catheter lies within the bladder. If no urine drains do not inflate the balloon, as the tip, and therefore the balloon, may still be in the urethra. Inflating the balloon at this point could lead to urethral injury. Documentation: Clearly document that the patient’s consent was obtained. Also document the volume of sterile water instilled into the balloon and the residual volume of urine, as well as any complications that occurred during the procedure. It may also be sensible to document the colour and quality of the urine produced. Catheter bag: After successful positioning of the catheter ensure it is draining adequately and that the correct type of urine collection bag is attached. • An urometer may be required to measure accurate hourly urine volumes • Various leg-bag attachments are available for the ambulant patient. Removal: Once the patient no longer requires the catheter, remove it as soon as possible to prevent infection. Deflate the balloon before removing the catheter. Male urethral catheterisation animated demonstration Equipment needed This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 25 TREATMENT • Latex or silicone Foley catheter (14 French gauge for general use; with prostatic hypertrophy a larger 16 French gauge may be easier to pass due to its greater rigidity; sizes from 12 French to 24 French may be needed depending on the situation) • Sterile drape • Sterile paper towel (preferably fenestrated) • Sterile gloves Abdominal aortic aneurysm • • • • • • Treatment Plastic apron Sterile pot Kidney dish 10 mL syringe filled with 10 mL sterile water (NOT saline) Lubricating anaesthetic gel (e.g., lignocaine gel) in a pre-filled 10 mL syringe Swabs and saline solution (not chlorhexidine or other cleaning solutions, as these can be irritating to the skin). Contraindications Do not perform urethral catheterisation after pelvic trauma, especially if there is suspicion of urethral injury that may accompany a pelvic fracture, for example. In patients with a urethral injury, there is a risk that the catheter may pass straight through the urethra and into the surrounding tissues. In these patients, arrange for further imaging of the urethra before attempting catheterisation. If you fail to insert a urethral catheter on two or more occasions, seek a more experienced clinician for assistance. It may be necessary to use a curved coude tip catheter, a smaller or larger catheter, or a three-way irrigation catheter. If the patient has capacity and refuses urethral catheterisation after sufficient communication and understanding, do not perform the procedure against their wishes. Phimosis, hypospadias, and penile deformity may make urethral catheterisation more difficult but they are not contraindications. Indications • • • • • • Acute retention of urine Perioperative urinary collection Accurate measurement of urine output in the acutely or critically unwell Re-insertion of a long-term urinary catheter Prostatic enlargement with chronic bladder obstruction Bladder irrigation or instillation. Patients with urinary incontinence and immobility may need catheterisation but these are not clear indications. Clinicians must balance the risk of infection against the convenience of the catheter. Complications TREATMENT • Failure to catheterise: seek help from a more experienced clinician • Urinary tract infection: remove the catheter and give antibiotics as directed by local policy • Bleeding: minor bleeding is common and generally stops spontaneously; for more significant urethral haemorrhage seek expert advice from a more experienced clinician • Creating a false passage: forceful catheterisation can lead to formation of blind ending passages making it increasingly difficult to catheterise the true urethra and creating traumatic bleeding; avoid using force during catheterisation at all times • Blocked catheter: may result from clots or other debris. Aspirating or flushing the catheter with sterile water may clear the lumen; however, repositioning may be required. The patient may need irrigation with a three-way catheter if haematuria and retention of clots recur. 26 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Treatment Abdominal aortic aneurysm Aftercare Documentation: Clearly document that the patient’s consent was obtained. Also document the volume of sterile water instilled into the balloon and the residual volume of urine. It may also be sensible to document the colour and quality of the urine produced, and whether there were any complications to the procedure. Catheter bag: After successful positioning of the catheter ensure it is draining adequately and that the correct type of urine collection bag is attached. • A urometer may be required to measure hourly urine volumes accurately • Leg-bag attachments are available for the ambulant patient. Removal: Once the patient no longer requires the catheter, remove it as soon as possible to prevent infection. Deflate the balloon before removing the catheter. Treatment details overview Consult your local pharmaceutical database for comprehensive drug information including contraindications, drug interactions, and alternative dosing. ( see Disclaimer ) Acute ( summary ) Patient group ruptured AAA symptomatic, but not ruptured AAA Tx line 1st Treatment standard resuscitation measures plus urgent surgical repair plus perioperative antibiotic therapy 1st semi-urgent surgical repair plus preoperative cardiovascular risk reduction plus perioperative antibiotic therapy Ongoing incidental finding: asymptomatic small AAA Tx line 1st Treatment TREATMENT Patient group ( summary ) surveillance This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 27 Treatment Abdominal aortic aneurysm Ongoing ( summary ) plus incidental finding: large AAA elective surgical repair plus preoperative cardiovascular risk reduction plus perioperative antibiotic therapy 1st corrective procedure plus preoperative cardiovascular risk reduction plus perioperative antibiotic therapy TREATMENT endovascular repair leak requiring treatment 1st aggressive cardiovascular risk management 28 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Treatment Abdominal aortic aneurysm Treatment options Acute Patient group ruptured AAA Tx line 1st Treatment standard resuscitation measures » The airway is managed with supplemental oxygen and endotracheal intubation. » A central venous catheter is inserted. » Monitoring requires insertion of an arterial catheter and urinary catheter. » A target systolic BP of 50 to 70 mmHg and withholding fluids is advocated preoperatively.[112] [117] [118] » Aggressive fluid replacement may cause dilutional and hypothermic coagulopathy and secondary clot disruption from increased blood flow, increased perfusion pressure, and decreased blood viscosity thereby exacerbating bleeding.[108] [112] [117] [118] Infusing more than 3.5 L of fluid preoperatively may increase the relative risk of death.[108] plus urgent surgical repair » Endovascular AAA repair (EVAR) is the most efficacious test for repair, aortoiliac anatomy permitting; otherwise, traditional open repair is performed.[1] [108] [112] [109] [110] [111] [113] » Operative mortality for open repair is 48%.[114] Despite frequent prolonged ICU and hospital lengths of stay, around 60% survive with long-term survival similar to that of the general population. Data support cost effectiveness.[114] [115] [116] plus perioperative antibiotic therapy » Antibiotic therapy is indicated for patients undergoing emergency repair of ruptured AAA to cover gram-positive and gram-negative organisms and prevent graft infection. symptomatic, but not ruptured AAA 1st semi-urgent surgical repair This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 29 TREATMENT » Broad-spectrum antibiotic coverage is tailored to patient clinical presentation and cultures, and in accordance with local protocols. Treatment Abdominal aortic aneurysm Acute Patient group Tx line Treatment » Aorto-iliac anatomy permitting, endovascular AAA repair (EVAR) may be offered to these patients. » Urgent open repair of symptomatic unruptured AAAs carries increased morbidity and mortality with a rate between that of ruptured AAA repair and elective repair.[1] [148] EVAR in this setting demonstrates promising results with lower firstmonth mortality.[1] [113] » Comorbid diseases are medically optimised.[1] [47] plus preoperative cardiovascular risk reduction » Preoperative beta-blockade may be reasonable in patients with intermediate- or high-risk myocardial ischaemia, and those with 3 or more RCRI (revised cardiac risk index) risk factors (e.g., diabetes mellitus, heart failure, CAD, renal insufficiency, stroke). When indicated, beta-blocker therapy should be started more than 1 day before surgery.[104] [105] » A short-acting beta-blocker such as metoprolol allows for dosing adjustment within a few days. Atenelol and propanolol have also been used. [1] [149] » Doses should preferably be started 2 to 7 days before surgery.[104] » Perioperative statin use reduces cardiovascular events.[104] » A large, multi-centre study of patients undergoing non-cardiac surgery found that clonidine did not reduce the rate of death or nonfatal myocardial infarction.[106] Alpha-2 agonists are not, therefore, recommended for non-cardiac surgery patients.[104] [104] plus perioperative antibiotic therapy TREATMENT » Perioperative antibiotic therapy is given. Broadspectrum antibiotic coverage is necessary, in accordance with local protocols. Ongoing Patient group 30 Tx line Treatment This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Treatment Abdominal aortic aneurysm Ongoing Patient group incidental finding: asymptomatic small AAA Tx line 1st Treatment surveillance » For AAA detected as an incidental finding, repair is deferred until the theoretical risk of rupture exceeds the estimated risk of operative mortality. Generally, repair is indicated in patients with large asymptomatic AAA (e.g., with a diameter exceeding 5.5 cm in men or 5.0 cm in women in the US), although treatment decisions based on greater size may differ in other countries (e.g., UK).[1] [74] [75] [76] [77] [78] » Surveillance with selective repair is most appropriate for older male patients with significant comorbidities. Young, healthy patients, and especially women, with AAA between 5.0 and 5.4 cm may benefit from early repair.[47] [74] [75] [76] [77] » Monitor infra-/juxtarenal AAAs measuring 4.0 to 5.4 cm in diameter with ultrasonography (USS)/CT every 6 to 12 months.[73] » AAAs <4.0 cm require USS every 2 to 3 years.[73] plus aggressive cardiovascular risk management » Patients should be encouraged to stop smoking and offered drug therapy to assist with this if needed. » Beta-blockers may be used to reduce the rate of aneurysm expansion, [47] [124] [125] [126] although clinical trials have not supported this. » Other modifiable cardiovascular risk factors (such as hyperlipidaemia) can be treated, and statins may be considered to reduce the risk of AAA enlargement.[47] incidental finding: large AAA 1st elective surgical repair This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 31 TREATMENT » Generally, repair is indicated in patients with large asymptomatic AAA (e.g., with a diameter exceeding 5.5 cm in men or 5.0 cm in women in the US), although treatment decisions based on greater size may differ in other countries (e.g., UK). Repair of aneurysms ≥5.5 cm offers a survival advantage.[1] [75] [76] [77] [78] Treatment Abdominal aortic aneurysm Ongoing Patient group Tx line Treatment » Young, healthy patients, and especially women, with AAA between 5.0 and 5.4 cm may benefit from early repair.[47] [74] [75] [76] [77] » Data suggest that in patients with large AAAs (ranging from 5 to 5.5 cm) undergoing elective repair, endovascular aneurysm repair (EVAR) is equivalent to open repair in terms of overall survival, although the rate of secondary interventions is higher for EVAR.[87] [88] EVAR also reduces AAA-related mortality (but not longer-term overall survival) in patients unsuitable for open repair.[89] » Patients with greater risk of perioperative morbidity and mortality (i.e., COPD, multiple previous abdominal operations) may benefit from a less invasive approach, aorto-iliac anatomy permitting. Younger, healthier patients may benefit from the durability of an open repair. Reasons for deferring care may include terminal illness (i.e., cancer) such that life expectancy is <6 to 12 months and patient choice. plus preoperative cardiovascular risk reduction » Preoperative beta-blockade may be reasonable in patients with intermediate- or high-risk myocardial ischaemia, and those with 3 or more RCRI (revised cardiac risk index) risk factors (e.g., diabetes mellitus, heart failure, CAD, renal insufficiency, stroke). When indicated, beta-blocker therapy should be started more than 1 day before surgery.[104] [105] » A short-acting beta-blocker such as metoprolol allows for dosing adjustment within a few days. Atenelol and propanolol have also been used. [1] [149] » Doses should preferably be started 2 to 7 days before surgery.[104] » Perioperative statin use reduces cardiovascular events.[104] TREATMENT » A large, multi-centre study of patients undergoing non-cardiac surgery found that clonidine did not reduce the rate of death or nonfatal myocardial infarction.[106] Alpha-2 agonists are not, therefore, recommended for non-cardiac surgery patients.[104] [104] plus 32 perioperative antibiotic therapy This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Treatment Abdominal aortic aneurysm Ongoing Patient group Tx line Treatment » Perioperative antibiotic therapy is given. Broadspectrum antibiotic coverage is necessary, in accordance with local protocols. endovascular repair leak requiring treatment 1st corrective procedure » Endoleak is persistent blood flow outside the graft and within the aneurysm sac.[127] [128] » Risk of endoleak following endovascular aneurysm repair (EVAR) is 24%.[127] Endoleak is not a complication following open repair. There are 5 types of endoleak and management is dependant upon type. » Type I: repair is indicated upon discovery (endovascular extension grafts or conversion to open repair if necessary).[47] [Fig-6] [Fig-7] » Type II: treatment remains controversial and is advocated either if persistent at 6 to 12 months or when aneurysm sac size increases.[130] [131] [132] [133] Treatment of choice is transarterial coil embolisation, although laparoscopic ligation of collateral branches, direct percutaneous translumbar puncture of the sac, translumbar embolisation, and transcatheter transcaval embolisation have been reported.[128] [130] [131] [132] [134] [135] [136] [137] » Type III: repair is indicated upon discovery (endovascular stent graft extension).[47] [131] » Type IV: these leaks are uncommon with newer stent grafts and are self-limited, requiring no treatment.[47] [131] » Type V: there is no standardised method to measure endotension or consensus on indicated therapy in the absence of aneurysm enlargement; however, treatment of endotension to prevent aneurysm rupture is suggested in selected patients with continued aneurysm expansion.[47] [128] preoperative cardiovascular risk reduction » Preoperative beta-blockade may be reasonable in patients with intermediate- or high-risk myocardial ischaemia, and those with 3 or more RCRI (revised cardiac risk This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 33 TREATMENT plus Treatment Abdominal aortic aneurysm Ongoing Patient group Tx line Treatment index) risk factors (e.g., diabetes mellitus, heart failure, CAD, renal insufficiency, stroke). When indicated, beta-blocker therapy should be started more than 1 day before surgery.[104] [105] » A short-acting beta-blocker such as metoprolol allows for dosing adjustment within a few days. Atenelol and propanolol have also been used. [1] [149] » Doses should preferably be started 2 to 7 days before surgery.[104] » Perioperative statin use reduces cardiovascular events.[104] » A large, multi-centre study of patients undergoing non-cardiac surgery found that clonidine did not reduce the rate of death or nonfatal myocardial infarction.[106] Alpha-2 agonists are not, therefore, recommended for non-cardiac surgery patients.[104] plus perioperative antibiotic therapy TREATMENT » Perioperative antibiotic therapy is given. Broadspectrum antibiotic coverage is necessary, in accordance with local protocols. 34 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Treatment Emerging Dox ycycline or roxithromycin Doxycycline is a non-specific inhibitor of matrix metalloproteinases (MMP) that promote degradation of collagen and elastin and are integral to aneurysm formation.[1] [14]Targeted gene disruption of MMP-9 in mice suppresses the development of experimental AAA and both MMP-2 and -9 are necessary to induce experimental AAA formation in mice.[150] [151] [152]Animal models have shown that continuous periaortic infusion of doxycycline lowers the effective dose, and can effectively suppress experimental AAAs serving as a prototype for adjuvant treatment modalities that complement endovascular AAA exclusion and may inhibit progressive expansion of aortic aneurysms.[1] [153] [154] One clinical trial has found that prolonged administration of doxycycline for 6 months is safe and well tolerated by patients with small asymptomatic AAAs and is associated with a gradual reduction in plasma MMP-9 levels.[1] [155]Another small randomised trial assessing the ability of doxycycline to inhibit the growth of aortic aneurysms noted no growth in doxycycline-treated patients at 6 and 12 months.[156] [157]Further studies are needed to evaluate the long-term effects of doxycycline on the rate and extent of aneurysm growth and the potential use of plasma MMP-9 levels as a biomarker of aneurysm disease progression, but there appear to be sufficient preliminary data to support a large prospective randomised trial of doxycycline to prevent aneurysm expansion.[156]At this time, however, insufficient data exist to recommend use of doxycycline or roxithromycin.[47] [158] TREATMENT This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 35 Follow up Abdominal aortic aneurysm FOLLOW UP Recommendations Monitoring In patients with small aneurysms, monitor infra-/juxtarenal AAAs measuring 4.0 to 5.4 cm in diameter with ultrasonography (USS)/CT every 6 to 12 months.[73]AAAs <4.0 cm require USS every 2 to 3 years.[73]Consider expansion rates, as some advocate expansion of 4 to 8 mm over 12 months suggests instability.[1] As late aneurysm formation may be noted in approximately 1%, 5%, and 20% of patients at 5, 10, and 15 years after open repair, respectively, follow-up non-contrast CT imaging at 5-year intervals is recommended.[47] Previous recommendations regarding post-endovascular repair (post-EVAR) surveillance included CT imaging at 1, 6, and 12 months postoperatively and yearly thereafter to evaluate for late graft complications (i.e., migration, occlusion, and endoleak).[44] However, more recent concerns regarding the frequent use of CT scanning, cost, and cumulative radiation exposure/potential lifetime cancer risk have resulted in a shift towards colour duplex ultrasound imaging for surveillance. Current recommendations include contrast-enhanced CT imaging at 1 and 12 months during the first year following EVAR. If neither endoleak nor AAA enlargement is documented during first year after EVAR, colour duplex ultrasonography is suggested as an alternative to CT imaging for annual postoperative surveillance with non-contrast CT imaging every 5 years.[47] [163] [153] Antibiotic prophylaxis of graft infection is required prior to bronchoscopy, gastrointestinal or genitourinary endoscopy, and any dental procedure that may lead to bleeding.[47] Generalised sepsis, groin drainage, pseudoaneurysm formation, or ill-defined pain after open repair or EVAR should prompt evaluation of graft infection.[47]GI bleeding after open repair or EVAR should prompt evaluation of an aortoenteric fistula.[47] Patient instructions Patients should be educated on the importance of smoking cessation (including counselling and pharmacotherapy as needed), and of blood pressure and cholesterol control. Complications Complications ureteral obstruction Timeframe long term Likelihood low Ureteric obstruction is related to encasement of the ureters in an inflammatory perianeurysmal fibrosis of unresolved aetiology rather than secondary to aneurysm compression.[160] Most often, ureteral compression is associated with inflammatory aortic aneurysm. Extensive retroperitoneal adhesions may result in ureteral obstruction in 18% of patients. The inferior vena cava may become involved as well.[161] functional gastric outlet obstruction long term low Duodenal obstruction is a consequence of compression of the duodenum in its fixed retroperitoneal course between the aneurysmal aorta and the superior mesenteric artery.[160] distal embolisation variable low Incidence is 3% to 29%, most commonly affecting the digits (blue toe syndrome). There is a 5% incidence of distal embolisation resulting in limb-threatening ischaemia, digital ischaemia, and calf myonecrosis.[162] 36 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Follow up Prognosis This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 37 FOLLOW UP The natural course involves slow and steady growth with ultimate progression to rupture. Most patients with rupture will not survive to reach the operating theatre; overall mortality is around 90%.[83] Given the morbidity and mortality associated with surgical intervention, repair is typically deferred until the theoretical risk of rupture exceeds the estimated risk of operative mortality. The majority of patients undergoing open repair remain without significant graft-related complications during the remainder of their lives (0.4% to 2.3% incidence of late graft-related complications).[1] [159] Five-year survival rates after intact aneurysm repair average 60% to 75%. Those undergoing endovascular repair (EVAR) are more likely to have a delayed complication and require re-intervention. Guidelines Abdominal aortic aneurysm Diagnostic guidelines Europe Abdominal aortic aneurysm screening: how it works Published by: Public Health England Last published: 2015 Summary: Provides information about the NHS AAA screening programme, and the tests and processes involved. North America GUIDELINES ACC/AHA guideline on perioperative cardiovascular evaluation and management of patients undergoing noncardiac surgery Published by: American College of Cardiology; American Heart Association Last published: 2014 Summary: Clinical practice guideline including recommendations about preoperative risk assessment and cardiac testing in the adult patient undergoing non-cardiac surgery. The care of patients with an abdominal aortic aneurysm: the Society for Vascular Surgery practice guidelines Published by: Society for Vascular Surgery Last published: 2009 Summary: Provides recommendations for patient evaluation and risk of rupture in AAA, and for selecting surgical or endovascular intervention, peri- and intra-operative strategies, follow-up, and treatment of complications. Treatment guidelines Europe Endovascular stent-grafts for the treatment of abdominal aortic aneurysms Published by: National Institute for Health and Care Excellence Last published: 2009 Summary: Provides an appraisal of the use of grafts in the treatment of AAA. Laparoscopic repair of abdominal aortic aneurysm Published by: National Institute for Health and Care Excellence Last published: 2007 Summary: These guidelines make recommendations on the laparoscopic repair of AAA. Recommendations are made on who should carry out the procedure, and the information given to patients and their Trust. 38 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Guidelines Europe Stent-graft placement in abdominal aortic aneurysm Published by: National Institute for Health and Care Excellence Last published: 2006 Summary: These guidelines make recommendations on the information clinicians should ensure patients understand about the procedure and the potential risks involved. The guidelines also advise on patient selection for the procedure. North America ACC/AHA guideline on perioperative cardiovascular evaluation and management of patients undergoing noncardiac surgery Published by: American College of Cardiology; American Heart Association Last published: 2014 GUIDELINES Summary: Guideline addressing pharmacotherapeutic and anaesthetic considerations for non-cardiac surgery patients. Management of patients with peripheral artery disease (compilation of 2005 and 2011 ACCF/AHA guideline recommendations) Published by: American College of Cardiology Foundation; American Heart Association Last published: 2013 Summary: Includes recommendations for the screening and management of patients with aneurysms of the abdominal aorta. The care of patients with an abdominal aortic aneurysm: the Society for Vascular Surgery practice guidelines Published by: Society for Vascular Surgery Last published: 2009 Summary: Provides recommendations for patient evaluation and risk of rupture in AAA, and for selecting surgical or endovascular intervention, peri- and intra-operative strategies, follow-up, and treatment of complications. This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 39 Abdominal aortic aneurysm References REFERENCES Key articles • Chaikof EL, Brewster DC, Dalman RL, et al; Society for Vascular Surgery. The care of patients with an abdominal aortic aneurysm: the Society for Vascular Surgery practice guidelines. J Vasc Surg. 2009;50(suppl 4):S2-S49. Full text Abstract • US Preventive Services Task Force. Final recommendation statement. Abdominal aortic aneurysm: screening. June 2014. http://www.uspreventiveservicestaskforce.org/ (last accessed 6 June 2017). Full text • Ferket BS, Grootenboer N, Colkesen EB, et al. Systematic review of guidelines on abdominal aortic aneurysm screening. J Vasc Surg. 2012;55:1296-1304. • Anderson JL, Halperin JL, Albert NM, et al. Management of patients with peripheral artery disease (compilation of 2005 and 2011 ACCF/AHA guideline recommendations): a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Circulation. 2013;127:1425-1443. Full text Abstract • De Bruin JL, Baas AF, Buth J, et al; DREAM Study Group. Long-term outcome of open or endovascular repair of abdominal aortic aneurysm. N Engl J Med. 2010;362:1881-1889. Abstract • United Kingdom EVAR Trial Investigators, Greenhalgh RM, Brown LC, et al. Endovascular versus open repair of abdominal aortic aneurysm. N Engl J Med. 2010;362:1863-1871. Abstract • United Kingdom EVAR Trial Investigators, Greenhalgh RM, Brown LC, et al. Endovascular repair of aortic aneurysm in patients physically ineligible for open repair. N Engl J Med. 2010;362:1872-1880. Abstract • Fleisher LA, Fleischmann KE, Auerbach AD, et al. 2014 ACC/AHA guideline on perioperative cardiovascular evaluation and management of patients undergoing noncardiac surgery: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation. 2014;130:e278-333. Full text Abstract References 1. Dehlin JM, Upchurch GR. Management of abdominal aortic aneurysms. Curr Treat Options Cardiovasc Med. 2005;7:119-130. Abstract 2. Johnston KW, Rutherford RB, Tilson MD, et al. Suggested standards for reporting on arterial aneurysms. J Vasc Surg. 1991;13:452-458. Abstract 3. McConathy WJ, Alaupovic P, Woolcock N, et al. Lipids and apolipoprotein profiles in men with aneurysmal and stenosing aorto-iliac atherosclerosis. Eur J Vasc Surg. 1989;3:511-514. Abstract 4. Saratzis A, Bown MJ. The genetic basis for aortic aneurysmal disease. Heart. 2014;100:916-922. Abstract 40 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm References Tang T, Boyle JR, Dixon AK, et al. Inflammatory abdominal aortic aneurysms. Eur J Vasc Endovasc. Surg. 2005;29:353-362. Abstract 6. Gomes MN, Choyke PL, Wallace RB. Infected aortic aneurysms: a changing entity. Ann Surg. 1992;215:435-442. Full text Abstract 7. Zankl AR, Schumacher H, Krumsdorf U, et al. Pathology, natural history and treatment of abdominal aortic aneurysms. Clin Res Cardiol. 2007;96:140-151. Abstract 8. Cosford PA, Leng GC. Screening for abdominal aortic aneurysm. Cochrane Database Syst Rev. 2007; (2):CD002945. Full text Abstract 9. Minino AM, Heron MP, Murphy SL, et al. Deaths: final data for 2004. Natl Vital Stat Rep. 2007;55:1-119. Full text 10. Solberg S, Singh K, Wilsgaard T, et al. Increased growth rate of abdominal aortic aneurysms in women. The Tromso Study. Eur J Vasc Endovasc Surg. 2005;29:145-149. Abstract 11. Singh K, Bonaa H, Jacobsen BK, et al. Prevalence of and risk factors for abdominal aortic aneurysms in a population-based study: The Tromsø Study. Am J Epidemiol. 2001;154:236-244. Full text Abstract 12. Lopez-Candales A, Holmes DR, Liao S, et al. Decreased vascular smooth muscle cell density in medial degeneration of human abdominal aortic aneurysms. Am J Pathol. 1997;150:993-1007. Full text Abstract 13. Wassef M, Baxter BT, Chisholm RL, et al. Pathogenesis of abdominal aortic aneurysms: a multidisciplinary research program supported by the National Heart, Lung, and Blood Institute. J Vasc Surg. 2001;34:730-738. Abstract 14. Ailawadi G, Eliason JL, Upchurch GR. Current concepts in the pathogenesis of abdominal aortic aneurysm. J Vasc Surg. 2003;38:584-588. Abstract 15. Davies MJ. Aortic aneurysm formation: lessons from human studies and experimental models. Circulation. 1998;98:193-195. Full text Abstract 16. Grange JJ, Davis V, Baxter BT. Pathogenesis of abdominal aortic aneurysm: an update and look toward the future. Cardiovasc Surg. 1997;5:256-265. Abstract 17. Takagi H, Manabe H, Kawai N, et al. Circulating matrix metalloproteinase-9 concentrations and abdominal aortic aneurysm presence: a meta-analysis. Interact Cardiovasc Thorac Surg. 2009;9:437-440. Full text Abstract 18. Stocker R, Keaney JF Jr. Role of oxidative modifications in atherosclerosis. Physiol Rev. 2004;84:1381-1478. Full text Abstract 19. Griendling KK, FitzGerald GA. Oxidative stress and cardiovascular injury: Part I: basic mechanisms and in vivo monitoring of ROS. Circulation. 2003;108:1912-1916. Full text Abstract This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 41 REFERENCES 5. REFERENCES Abdominal aortic aneurysm References 20. Griendling KK, FitzGerald GA. Oxidative stress and cardiovascular injury: Part II: animal and human studies. Circulation. 2003;108:2034-2040. Full text Abstract 21. McCormick ML, Gavrila D, Weintraub NL. Role of oxidative stress in the pathogenesis of abdominal aortic aneurysms. Arterioscler Thromb Vasc Biol. 2007;27:461-469. Abstract 22. Ailawadi G, Knipp BS, Lu G, et al. A nontrinsic regional basis for increased infrarenal aortic MMP-9 expression and activity. J Vasc Surg. 2003;37:1059-1066. Abstract 23. Moore JE, Ku DN, Zarins CK, et al. Pulsatile flow visualization in the abdominal aorta under differing conditions: implications for increased susceptibility to atherosclerosis. J Biomech Eng. 1992;114:391-397. Abstract 24. Tung WS, Lee JK, Thompson RW. Simultaneous analysis of 1176 gene products in normal human aorta and abdominal aortic aneurysms using a membrane-based complementary DNA expression array. J Vasc Surg. 2000;34:143-150. Full text 25. Shibamura H, Olson JM, van Vlijmen-Van Keulen C, et al. Genome scan for familial abdominal aortic 26. Lederle, FA, Johnson GR, Wilson SE, et al. Prevalence and associations of abdominal aortic aneurysm detected through screening. Ann Intern Med. 1997;26:441-449. Abstract 27. Wilmink TB, Quick CR, Day NE. The association between cigarette smoking and abdominal aortic aneurysms. J Vasc Surg. 1999;30:1099-1105. Abstract 28. Rasmussen TE, Hallett JW Jr, Tazelaar HD, et al. Human leukocyte antigen class II immune response genes, female gender, and cigarette smoking as risk and modulating factors in abdominal aortic aneurysms. J Vasc Surg. 2002;35:988-993. Abstract 29. Kuivaniemi H, Shibamura H, Arthur C, et al. Familial abdominal aortic aneurysms: Collection of 233 multiplex families. J Vasc Surg. 2003;37:340-345. Abstract 30. Majumder PP, St Jean PL, Ferrell RE, et al. On the inheritance of abdominal aortic aneurysm. Am J Hum Genet. 1991;48:164-170. Full text Abstract 31. Verloes A, Sakalihasan N, Koulischer L, et al. Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees. J Vasc Surg. 1995;21:646-655. Full text Abstract 32. Johansen K, Koepsell T. Familial tendency for abdominal aortic aneurysms. JAMA. 1986;256:1934-1936. Abstract 33. Ogata T, MacKean GL, Cole CW, et al. The lifetime prevalence of abdominal aortic aneurysms among siblings of aneurysm patients is eightfold higher than among siblings of spouses: an analysis of 187 aneurysm families in Nova Scotia, Canada. J Vasc Surg. 2005;42:891-897. Full text Abstract 34. Darling RC 3rd, Brewster DC, Darling RC, et al. Are familial abdominal aortic aneurysms different? J Vasc Surg. 1989;10:39-43. Abstract 42 aneurysm using sex and family history as covariates suggests genetic heterogeneity and identifies linkage to chromosome 19q13. Circulation. 2004;109:2103-2108. Full text Abstract This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm References Webster MW, Ferrell RE, St Jean PL, et al. Ultrasound screening of first-degree relatives of patients with an abdominal aortic aneurysm. J Vasc Surg. 1991;13:9-13. Abstract 36. Van der Vliet JA, Boll AP. Abdominal aortic aneurysm. Lancet. 1997;349:863-866. Abstract 37. Golledge J, Clancy P, Jamrozik K, et al. Obesity, adipokines, and abdominal aortic aneurysm. Heath in men study. Circulation. 2007;116:2275-2279. Abstract 38. Grootenboer N, Bosch JL, Hendriks JM, et al. Epidemiology, aetiology, risk of rupture and treatment of abdominal aortic aneurysms: does sex matter? Eur J Vasc Endovasc Surg. 2009;38:278-284. Abstract 39. Hollister DW, Godfrey M, Sakai LY, et al. Immunohistologic abnormalities of the microfibrillar-fiber system in the Marfan syndrome. N Engl J Med. 1990;323:152-159. Abstract 40. Dietz HC, Cutting GR, Pyeritz RE, et al. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene. Nature. 1991;352:337-339. Abstract 41. Jeremy RW, Huang H, Hwa J, et al. Relation between age, arterial distensibility, and aortic dilatation in 42. Fowkes FG, Anandan CL, Lee AJ, et al. Reduced lung function in patients with abdominal aortic aneurysm is associated with activation of inflammation and hemostasis, not smoking or cardiovascular disease. J Vasc Surg. 2006 ;43:474-480. Abstract 43. Brown LC, Powell JT. Risk factors for aneurysm rupture in patients kept under ultrasound surveillance. Ann Surg. 1999;230:289-296. Full text Abstract 44. Upchurch GR, Schaub TA. Abdominal aortic aneurysm. Am Fam Physician. 2006;73:1198-1204. Full text Abstract 45. Chang JB, Stein TA, Liu JP, et al. Risk factors associated with rapid growth of small abdominal aortic aneurysms. Surgery. 1997;121:117-122. Abstract 46. Englesbe MJ, Wu AH, Clowes AW, et al. The prevalence and natural history of aortic aneurysms in heart and abdominal organ transplant patients. J Vasc Surg. 2003;37:27-31. Full text Abstract 47. Chaikof EL, Brewster DC, Dalman RL, et al; Society for Vascular Surgery. The care of patients with an abdominal aortic aneurysm: the Society for Vascular Surgery practice guidelines. J Vasc Surg. 2009;50(suppl 4):S2-S49. Full text Abstract 48. Fink HA, Lederle FA, Roth CS, et al. The accuracy of physical examination to detect abdominal aortic aneurysm. Arch Intern Med. 2000;160:833-836. Full text Abstract 49. Lindholt JS, Vammen S, Juul S, et al. The validity of ultrasonographic scanning as screening method for abdominal aortic aneurysm. Eur J Vasc Endovasc Surg. 1999;17:472-475. Abstract 50. Fillinger MF, Marra SP, Raghavan ML, et al. Prediction of rupture risk in abdominal aortic aneurysm during observation: wall stress versus diameter. J Vasc Surg. 2003;37:724-732. Abstract the Marfan syndrome. Am J Cardiol. 1994;74:369-373. Abstract This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 43 REFERENCES 35. REFERENCES Abdominal aortic aneurysm References 51. Vowden P, Wilkinson D, Ausobsky JR, et al. A comparison of three imaging techniques in the assessment of an abdominal aortic aneurysm. J Cardiovasc Surg. 1989;30:891-896. Abstract 52. Taylor SM, Mills JL, Fujitani RM. The juxtarenal abdominal aortic aneurysm: a more common problem than previously realized? Arch Surg. 1994;129:734-737. Abstract 53. Rakita D, Newatia A, Hines JJ, et al. Spectrum of CT findings in rupture and impending rupture of abdominal aortic aneurysms. Radiographics. 2007;27:497-507. Abstract 54. Jacobs DO. Clinical practice: diverticulitis. N Engl J Med. 2007;357:2057-2066. Abstract 55. Scheinman SJ. Urinary calculi. Medicine. 2003:31:77-80. 56. Spiller R. Clinical update: irritable bowel syndrome. Lancet. 2007;369:1586-1588. Abstract 57. Nikolaus S, Schreiber S. Diagnostics of inflammatory bowel disease. Gastroenterology. 2007;133:1670-1689. Abstract 58. Oelsner G, Shashar D. Adnexal torsion. Clin Obstet Gynecol. 2006;49:459-463. Abstract 59. Stanley JC. Mesenteric arterial occlusive and aneurismal disease. Cardiol Clin. 2002;20:611-622. Abstract 60. Swedish Council on Technology Assessment in Health Care. Screening for abdominal aortic aneurysm. SBU Alert Report No 2008-04. September 2008. http://www.sbu.se/ Full text 61. Bockler, D, Lang W, Debus I, et al. Randomised studies with EBM level 1 prove it: a screening programme for abdominal aortic aneurysms makes sense [in German]. Gefasschirurgie. 2009;14:350-361. 62. Eckstein HH, Böckler D, Flessenkämper I, et al. Ultrasonographic screening for the detection of abdominal aortic aneurysms. Dtsch Arztebl Int. 2009;106:657-663. Full text Abstract 63. US Preventive Services Task Force. Final recommendation statement. Abdominal aortic aneurysm: screening. June 2014. http://www.uspreventiveservicestaskforce.org/ (last accessed 6 June 2017). Full text 64. Ashton HA, Buxton MJ, Day NE, et al. The Multicentre Aneurysm Screening Study (MASS) into the effect of abdominal aortic aneurysm screening on mortality in men: a randomised controlled trial. Lancet. 2002;360:1531-1539. Abstract 65. Lindholt JS, Juul S, Fasting H, et al. Hospital costs and benefits of screening for abdominal aortic aneurysms. Results from a randomised population screening trial. Eur J Vasc Endovasc Surg. 2002;23:55-60. Abstract 66. Norman PE, Jamrozik K, Lawrence-Brown MM, et al. Population based randomised controlled trial on impact of screening on mortality from abdominal aortic aneurysm. BMJ. 2004;329:1259. Abstract 44 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm References Scott RA, Bridgewater SG, Ashton HA. Randomized clinical trial of screening for abdominal aortic aneurysm in women. Br J Surg. 2002;89:283-285. Abstract 68. Scott RA, Wilson NM, Ashton HA, et al. Influence of screening on the incidence of ruptured abdominal aortic aneurysm: 5-year results of a randomized controlled study. Br J Surg. 1995;82:1066-1070. Abstract 69. Vardulaki KA, Walker NM, Couto E, et al. Late results concerning feasibility and compliance from a randomized trial of ultrasonographic screening for abdominal aortic aneurysm. Br J Surg. 2002;89:861-864. Abstract 70. Takagi H, Goto SN, Matsui M, et al. A further meta-analysis of population-based screening for abdominal aortic aneurysm. J Vasc Surg. 2010;52:1103-1108. Full text Abstract 71. Ferket BS, Grootenboer N, Colkesen EB, et al. Systematic review of guidelines on abdominal aortic aneurysm screening. J Vasc Surg. 2012;55:1296-1304. 72. Derubertis BG, Trocciola SM, Ryer EJ, et al. Abdominal aortic aneurysm in women: prevalence, risk 73. Anderson JL, Halperin JL, Albert NM, et al. Management of patients with peripheral artery disease (compilation of 2005 and 2011 ACCF/AHA guideline recommendations): a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Circulation. 2013;127:1425-1443. Full text Abstract 74. Lederle FA, Wilson SE, Johnson GR, et al. Immediate repair compared with surveillance of small abdominal aortic aneurysms. N Engl J Med. 2002;346:1437-1444. Abstract 75. The UK Small Aneurysm Trial Participants. Mortality results for randomized controlled trial of early elective surgery or ultrasonographic surveillance for small abdominal aortic aneurysms. Lancet. 1998;352:1649-1655. Abstract 76. United Kingdom Small Aneurysm Trial Participants. Long-term outcomes of immediate repair compared with surveillance of small abdominal aortic aneurysms. N Engl J Med. 2002;346:1445-1452. Full text Abstract 77. Powell JT, Brown LC, Forbes JF, et al. Final 12-year follow-up of surgery versus surveillance in the UK Small Aneurysm Trial. Br J Surg. 2007;94:702-708. Abstract 78. Brewster DC, Cronenwett JL, Hallett JW Jr, et al. Guidelines for the treatment of abdominal aortic aneurysms: report of a subcommittee of the Joint Council of the American Association for Vascular Surgery and Society for Vascular Surgery. J Vasc Surg. 2003;37:1106-1117. Abstract 79. Eliason JL, Upchurch GR. Endovascular abdominal aortic aneurysms repair. Circulation. 2008;117:1738-1744. Full text 80. Cambria RP, Brewster DC, Abbott WM, et al. Transperitoneal versus retroperitoneal approach for aortic reconstruction: a randomized prospective study. J Vasc Surg. 1990;11:314-324. Abstract factors, and implications for screening. J Vasc Surg. 2007;46:630-635. Abstract This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 45 REFERENCES 67. REFERENCES Abdominal aortic aneurysm References 81. Sicard GA, Reilly JM, Rubin BG, et al. Transabdominal versus retroperitoneal incision for abdominal aortic surgery: report of a prospective randomized trial. J Vasc Surg. 1995;21:174-181. Abstract 82. Senekowitsch C, Assadian A, Assadian O, et al. Replanting the inferior mesentery artery during infrarenal aortic aneurysm repair: influence on postoperative colon ischemia. J Vasc Surg. 2006;43:689-694. Abstract 83. Hirsch AT, Haskal ZJ, Hertzer NR, et al. ACC/AHA 2005 practice guidelines for the management of patients with peripheral arterial disease (lower extremity, renal, mesenteric, and abdominal aortic). Circulation. 2006;113:e463-e654. Full text Abstract 84. Johnston KW. Multicenter prospective study of nonruptured abdominal aortic aneurysms in patients refusing or unfit for elective repair. J Vasc Surg. 1989;9:437-447. Abstract 85. Eliason JL, Wainess RM, Dimick JB, et al. The effect of secondary operations on mortality following abdominal aortic aneurysm repair in the United States: 1988-2001. Vasc Endovasc Surg. 2005;39:465-472. Abstract 86. Parodi JC, Palmaz JC, Barone HD. Transfemoral intraluminal graft implantation for abdominal aortic aneurysms. Ann Vasc Surg. 1991;5:491-499. Abstract 87. De Bruin JL, Baas AF, Buth J, et al; DREAM Study Group. Long-term outcome of open or endovascular repair of abdominal aortic aneurysm. N Engl J Med. 2010;362:1881-1889. Abstract 88. United Kingdom EVAR Trial Investigators, Greenhalgh RM, Brown LC, et al. Endovascular versus open repair of abdominal aortic aneurysm. N Engl J Med. 2010;362:1863-1871. Abstract 89. United Kingdom EVAR Trial Investigators, Greenhalgh RM, Brown LC, et al. Endovascular repair of aortic aneurysm in patients physically ineligible for open repair. N Engl J Med. 2010;362:1872-1880. Abstract 90. Moore WS, Matsumura JS, Makaroun MS, et al. Five-year interim comparison of the Guidant bifurcated endograft with open repair of abdominal aortic aneurysm. J Vasc Surg. 2003;38:46-55. Abstract 91. Lee WA, Carter JW, Upchurch G, et al. Perioperative outcomes after open and endovascular repair of intact abdominal aortic aneurysms in the United States during 2001. J Vasc Surg. 2004;39:491-496. Abstract 92. Elkouri S, Gloviczki P, McKusick MA, et al. Perioperative complications and early outcome after endovascular and open surgical repair of abdominal aortic aneurysms. J Vasc Surg. 2004;39:497-505. Abstract 93. EVAR trial participants. Endovascular aneurysm repair versus open repair in patients with abdominal aortic aneurysm (EVAR trial 1): randomized controlled trial. Lancet. 2005;365:2179-2186. 94. EVAR trial participants. Endovascular aneurysm repair and outcome in patients unfit for open repair of abdominal aortic aneurysm (EVAR trial 2): randomized controlled trial. Lancet. 2005;365:2187-2192. 46 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm References Blankensteijn JD, de Jong SE, Prinssen M, et al. Two-year outcomes after conventional or endovascular repair of abdominal aortic aneurysms. N Engl J Med. 2005;352:2298-2405. Abstract 96. Lederle FA, Freischlag JA, Kyriakides TC, et al; Open Versus Endovascular Repair (OVER) Veterans Affairs Cooperative Study Group. Outcomes following endovascular vs open repair of abdominal aortic aneurysm: a randomized trial. JAMA. 2009;302:1535-1542. 97. Lederle FA, Freischlag JA, Kyriakides TC, et al; OVER Veterans Affairs Cooperative Study Group. Long-term comparison of endovascular and open repair of abdominal aortic aneurysm. N Engl J Med. 2012;367:1988-1897. Abstract 98. Schermerhorn ML, O’Malley AJ, Jhaveri A, et al. Endovascular vs. open repair of abdominal aortic aneurysms in the Medicare population. N Engl J Med. 2008;358:464-474. Abstract 99. Franks SC, Sutton AJ, Bown MJ, et al. Systematic review and meta-analysis of 12 years of endovascular abdominal aortic aneurysm repair. Eur J Vasc Endovasc Surg. 2007;33:154-171. Abstract 100. Farahmand P, Becquemin JP, Desgranges P, et al. Is hypogastric artery embolization during endovascular aortoiliac aneurysm repair (EVAR) innocuous and useful? Eur J Vasc Endovasc Surg. 2008;35:429-435. Abstract 101. Mehta M, Veith FJ, Ohki T, et al. Unilateral and bilateral hypogastric artery interruption during aortoiliac aneurysm repair in 154 patients: a relatively innocuous procedure. J Vasc Surg. 2001;33(2 Suppl):S27-S32. Abstract 102. Kouvelos GN, Katsargyris A, Antoniou GA, et al. Outcome after interruption or preservation of internal iliac artery flow during endovascular repair of abdominal aorto-iliac aneurysms. Eur J Vasc Endovasc Surg. 2016;52:621-634. Abstract 103. Bani-Hani MG, AL Khaffaf H, Titi MA, et al. Interventions for preventing venous thromboembolism following abdominal aortic surgery. Cochrane Database Syst Rev. 2008;(1):CD005509. Full text Abstract 104. Fleisher LA, Fleischmann KE, Auerbach AD, et al. 2014 ACC/AHA guideline on perioperative cardiovascular evaluation and management of patients undergoing noncardiac surgery: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation. 2014;130:e278-333. Full text Abstract 105. Wijeysundera DN, Duncan D, Nkonde-Price C, et al. Perioperative beta blockade in noncardiac surgery: a systematic review for the 2014 ACC/AHA guideline on perioperative cardiovascular evaluation and management of patients undergoing noncardiac surgery: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation. 2014;130:2246-2264. Full text Abstract 106. Devereaux PJ, Mrkobrada M, Sessler DI, et al. Aspirin in patients undergoing noncardiac surgery. N Engl J Med. 2014;370:1494-1503. Full text Abstract This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 47 REFERENCES 95. Abdominal aortic aneurysm References REFERENCES 107. Harkin DW, Dillon M, Blair PH, et al. Endovascular ruptured abdominal aortic aneurysm repair (EVRAR): a systematic review. Eur J Vasc Endovasc Surg. 2007;34:673-681. Abstract 108. Crawford ES. Ruptured aortic aneurysm. J Vasc Surg. 1991;13:348-350. Abstract 109. Palda VA, Detsky AS. Perioperative assessment and management of risk from coronary artery disease. Ann Intern Med. 1997;127:313-328. Abstract 110. Karkos CD, Harkin DW, Giannakou A, et al. Mortality after endovascular repair of ruptured abdominal aortic aneurysms: a systematic review and meta-analysis. Arch Surg. 2009;144:770-778. Full text Abstract 111. Veith FJ, Ohki T, Lipsitz EC, et al. Treatment of ruptured abdominal aneurysms with stent grafts: a new gold standard? Semin Vasc Surg. 2003; 16:171-175. Abstract 112. Roberts K, Revell M, Youssef H, et al. Hypotensive resuscitation in patients with ruptured abdominal aortic aneurysm. Eur J Vasc Endovasc Surg. 2006;31:339-344. Abstract 113. Peppelenbosch N, Yilmaz N, van Marrewijk C, et al. Emergency treatment of acute symptomatic or ruptured abdominal aortic aneurysm. Outcome of a prospective intent-to-treat by EVAR protocol. Eur J Vasc Endovasc Surg. 2003;26:303-310. Abstract 114. Bown MJ, Sutton AJ, Bell PRF, et al. A meta-analysis of 50 years of ruptured abdominal aortic aneurysm repair. Br J Surg. 2002;89:714-730. 115. Cho Js, Gloviczki P, Martelli E, et al. Long-term survival and late complications after repair of ruptured abdominal aortic aneurysms. J Vasc Surg. 1998;27:813-819. 116. Patel ST, Korn P, Haser PB, et al. The cost-effectiveness of repairing ruptured abdominal aortic aneurysms. J Vasc Surg. 2000;32:247-257. 117. Hardman DT, Fisher CM, Patel MI, et al. Ruptured abdominal aortic aneurysms: who should be offered surgery. J Vasc Surg. 1996;23:123-129. Abstract 118. Ohki T, Veith FJ. Endovascular grafts and other image-guided catheter-based adjuncts to improve the treatment of ruptured aortoiliac aneurysms. Ann Surg. 2000;232:466-479. Abstract 119. Filardo G, Powell JT, Martinez MA, et al. Surgery for small asymptomatic abdominal aortic aneurysms. Cochrane Database Syst Rev. 2015;(2):CD001835. Full text Abstract 120. Cao P. Comparison of surveillance vs Aortic Endografting for Small Aneurysm Repair (CAESAR) trial: study design and progress. Eur J Vasc Endovasc Surg 2005;30:245-251. Abstract 121. Stead LF, Perera R, Bullen C, et al. Nicotine replacement therapy for smoking cessation. Cochrane Database Syst Rev. 2012;(11):CD000146. Full text Abstract 122. Rigotti NA, Clair C, Munafò MR, et al. Interventions for smoking cessation in hospitalised patients. Cochrane Database Syst Rev. 2012;(5):CD001837. Full text Abstract 48 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm References 123. Hughes JR, Stead LF, Hartmann-Boyce J, et al. Antidepressants for smoking cessation. Cochrane Database Syst Rev. 2014;(1):CD000031. Full text Abstract REFERENCES 124. Leach SD, Toole AL, Stern H. Effect of beta-adrenergic blockade on the growth rate of abdominal aortic aneurysms. Arch Surg. 1988;123:606-609. Abstract 125. Lindholt JS, Fasting H, Juul S, et al. Impaired results of a randomized double blinded trial of propranolol versus placebo on the expansion rate of small abdominal aortic aneurysms. Int Angiol. 1999;18:52-57. Abstract 126. Propranolol Aneurysm Trial Investigators. Propranolol for small abdominal aortic aneurysms: results of a randomized trial. J Vasc Surg. 2002;35:72-79. Abstract 127. Schurink GW, Aarts NJ, vanBockel JH. Endoleak after stent-graft treatment of abdominal aortic aneurysm: a meta-analysis of clinical studies. Br J Surg. 1999;86:581-587. Abstract 128. Veith FJ, Baum RA, Ohki T, et al. Nature and significance of endoleaks and endotension: summary of opinions expressed at an international conference. J Vasc Surg. 2002;35:1029-1065. Abstract 129. Higashiura W, Greenberg RK, Katz E, et al. Predictive factors, morphologic effects, and proposed treatment paradigm for type II endoleaks after repair of infrarenal abdominal aortic aneurysms. J Vasc Interv Radiol. 2007;18:975-981. Abstract 130. Mansueto G, Cenzi D, Scuro A, et al. Treatment of type II endoleak with a transcatheter transcaval approach: results at 1-year follow-up. J Vasc Surg. 2007;45:1120-1127. Abstract 131. Baum RA, Stavropoulos SW, Fairman RM, et al. Endoleaks after endovascular repair of abdominal aortic aneurysms. J Vasc Interv Radiol. 2003;14:1111-1117. Abstract 132. Van Marrewijk CJ, Fransen G, Laheij RJ, et al. Is a type II endoleak after EVAR a harbinger of risk? Causes and outcome of open conversion and aneurysm rupture during follow-up. Eur J Vasc Endovasc Surg. 2004;27:128-137. Abstract 133. Harris PL, Vallabhaneni SR, Desgranges P, et al. Incidence and risk factors of late rupture, conversion, and death after endovascular repair of infrarenal aortic aneurysms: the EUROSTAR experience. J Vasc Surg. 2000;32:739-749. Abstract 134. Steinmetz E, Rubin BG, Sanchez LA, et al. Type II endoleak after endovascular abdominal aortic aneurysm repair: a conservative approach with selective intervention is safe and cost-effective. J Vasc Surg. 2004;39:306-313. Abstract 135. Baum RA, Cope C, Fairman, et al. Translumbar embolization of type 2 endoleaks after endovascular repair of abdominal aortic aneurysms. J Vasc Interv Radiol. 2001;12:111-116. Abstract 136. Baum RA, Carpenter JP, Golden MA, et al. Treatment of type 2 endoleaks after endovascular repair of abdominal aortic aneurysms: comparison of transarterial and translumbar techniques. J Vasc Surg. 2002;35:23-29. Abstract This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 49 Abdominal aortic aneurysm References REFERENCES 137. Schmid R, Gurke L, Aschwanden M, et al. CT-guided percutaneous embolization of a lumbar artery maintaining a type II endoleak. J Endovasc Ther. 2002;9:198-202. Abstract 138. Soar J, Nolan JP, Böttiger BW, et al. European Resuscitation Council guidelines for resuscitation 2015: Section 3. Adult advanced life support. Resuscitation. 2015;95:100-147. 139. Kusminsky RE. Complications of central venous catheterization. J Am Coll Surg. 2007;204:681-696. 140. McGee DC, Gould MK. Preventing complications of central venous catheterization. N Engl J Med. 2003;348:1123-1133. Full text 141. Smith RN, Nolan JP. Central venous catheters. BMJ. 2013;347:f6570. 142. Reich DL. Monitoring in anesthesia and perioperative care. Cambridge: Cambridge University Press; 2011. 143. Abbott Northwestern Hospital Internal Medicine Residency. Internal jugular central venous line. 2015. http://www.anwresidency.com (last accessed 27 October 2017). Full text 144. Bishop L, Dougherty L, Bodenham A, et al. Guidelines on the insertion and management of central venous access devices in adults. Int J Lab Hematol. 2007;29:261-278. 145. Fletcher SJ, Bodenham AR. Safe placement of central venous catheters: where should the tip of the catheter lie? Br J Anaesth. 2000;85:188-191. 146. Gibson F, Bodenham A. Misplaced central venous catheters: applied anatomy and practical management. Br J Anaesth. 2013;110:333-346. Full text 147. Schuster M, Nave H, Piepenbrock S, Pabst R, Panning B. The carina as a landmark in central venous catheter placement. Br J Anaesth. 2000;85:192-194. 148. Sullivan CA, Rohrer MJ, Culter BS. Clinical management of the symptomatic but unruptured abdominal aortic aneurysm. Surgery. 1990;11:799-803. Abstract 149. Fleisher LA, Eagle KA. Clinical practice. Lowering cardiac risk in noncardiac surgery. N Engl J Med. 2001;345:1677-1682. Abstract 150. Raffetto JD, Khalil RA. Matrix metalloproteinases and their inhibitors in vascular remodeling and vascular disease. Biochem Pharmacol. 2008;75:346-359. 151. Pyo R, Lee JK, Shipley JM, et al. Targeted gene disruption of matrix metalloproteinase-9 (gelatinase B) suppresses development of experimental abdominal aortic aneurysms. J Clin Invest. 2000;105:1641-1649. 152. Longo GM, Xiong W, Greiner TC, et al. Matrix metalloproteinases 2 and 9 work in concert to produce aortic aneurysms. J Clin Invest. 2002;110:625-632. 153. Sho E, Chu J, Sho M, et al. Continuous periaortic infusion improves doxycycline efficacy in experimental aortic aneurysms. J Vasc Surg. 2004;39:1312-1321. 50 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm References 155. Baxter BT, Pearce WH, Waltke EA, et al. Prolonged administration of doxycycline in patients with small asymptomatic abdominal aortic aneurysms: report of a prospective (Phase II) multicenter study. J Vasc Surg. 2002;36:1-12. Abstract 156. Rentschler M, Baxter BT. Pharmacological approaches to prevent abdominal aortic aneurysm enlargement and rupture. Ann N Y Acad Sci. 2006;1085:39-46. Abstract 157. Mosorin M, Juvonen J, Biancari F, et al. Use of doxycycline to decrease the growth rate of abdominal aortic aneurysms: a randomized, double-blind, placebo-controlled pilot study. J Vasc Surg. 2001;34:606-610. Abstract 158. Dodd BR, Spence RA. Doxycycline inhibition of abdominal aortic aneurysm growth: a systematic review of the literature. Curr Vasc Pharmacol. 2011;9:471-478. Abstract 159. Hertzer NR, Mascha EJ, Karafa MT, et al. Open infrarenal abdominal aortic aneurysm repair: the Cleveland Clinic experience from 1989 to 1998. J Vasc Surg. 2002;35:1145-1154. Abstract 160. Hodgson KJ, Webster DJ. Abdominal aortic aneurysm causing duodenal and ureteric obstruction. J Vasc Surg. 1986;3:364-368. Abstract 161. Kashyap VS, Fang R, Fitzpatrick CM, et al. Caval and ureteral obstruction secondary to an inflammatory abdominal aortic aneurysm. J Vasc Surg. 2003;38:1416-1421. Abstract 162. Baxter BT, McGee GS, Flinn WR, et al. Distal embolization as a presenting symptom of aortic aneurysms. Am J Surg. 1990;160:197-201. Abstract 163. Bevis PM, Cooper DG. Duplex ultrasound for surveillance after endovascular repair of abdominal aortic aneurysm. Ital J Vasc Endovasc Surg. 2012;19:237-243 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 51 REFERENCES 154. Bartoli MA, Parodi FE, Chu J, et al. Localized administration of doxycycline suppresses aortic dilatation in an experimental mouse model of abdominal aortic aneurysm. Ann Vasc Surg. 2006;20:228-236. Abdominal aortic aneurysm Images Images Figure 1: Ultrasound of a 3.8 cm x 4.2 cm AAA IMAGES University of Michigan, specifically the cases of Dr Upchurch reflecting the Departments of Vascular Surgery and Radiology Figure 2: Various endovascular stent grafts used for endovascular repair (EVAR) University of Michigan, specifically the cases of Dr Upchurch reflecting the Departments of Vascular Surgery and Radiology 52 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Images IMAGES Figure 3: Endovascular repair (EVAR) University of Michigan, specifically the cases of Dr Upchurch reflecting the Departments of Vascular Surgery and Radiology This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 53 Images IMAGES Abdominal aortic aneurysm Figure 4: CT scan of a ruptured AAA University of Michigan, specifically the cases of Dr Upchurch reflecting the Departments of Vascular Surgery and Radiology 54 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Images IMAGES Figure 5: Type I endoleak at the distal left iliac anastomosis (leak encircled) University of Michigan, specifically the cases of Dr Upchurch reflecting the Departments of Vascular Surgery and Radiology This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 55 Images IMAGES Abdominal aortic aneurysm Figure 6: Extension stent graft deployed for the same type I endoleak (encircled) University of Michigan, specifically the cases of Dr Upchurch reflecting the Departments of Vascular Surgery and Radiology 56 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Images IMAGES Figure 7: Resolution of the type I endoleak resolved after extension deployed University of Michigan, specifically the cases of Dr Upchurch reflecting the Departments of Vascular Surgery and Radiology This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 57 Images IMAGES Abdominal aortic aneurysm Figure 8: Type II endoleak (encircled) discovered on follow-up CT University of Michigan, specifically the cases of Dr Upchurch reflecting the Departments of Vascular Surgery and Radiology 58 This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. Abdominal aortic aneurysm Disclaimer Disclaimer This content is meant for medical professionals situated outside of the United States and Canada. The BMJ Publishing Group Ltd ("BMJ Group") tries to ensure that the information provided is accurate and up-todate, but we do not warrant that it is nor do our licensors who supply certain content linked to or otherwise accessible from our content. The BMJ Group does not advocate or endorse the use of any drug or therapy contained within nor does it diagnose patients. Medical professionals should use their own professional judgement in using this information and caring for their patients and the information herein should not be considered a substitute for that. This information is not intended to cover all possible diagnosis methods, treatments, follow up, drugs and any contraindications or side effects. In addition such standards and practices in medicine change as new data become available, and you should consult a variety of sources. We strongly recommend that users independently verify specified diagnosis, treatments and follow up and ensure it is appropriate for your patient within your region. In addition, with respect to prescription medication, you are advised to check the product information sheet accompanying each drug to verify conditions of use and identify any changes in dosage schedule or contraindications, particularly if the agent to be administered is new, infrequently used, or has a narrow therapeutic range. You must always check that drugs referenced are licensed for the specified use and at the specified doses in your region. This information is provided on an "as is" basis and to the fullest extent permitted by law the BMJ Group and its licensors assume no responsibility for any aspect of healthcare administered with the aid of this information or any other use of this information. View our full Website Terms and Conditions. DISCLAIMER This PDF of the BMJ Best Practice topic is based on the web version that was last updated: Nov 13, 2017. BMJ Best Practice topics are regularly updated and the most recent version of the topics can be found on bestpractice.bmj.com . Use of this content is subject to our disclaimer. © BMJ Publishing Group Ltd 2018. All rights reserved. 59 Contributors: // Authors: Maureen K. Sheehan, MD Assistant Professor Department of Surgery, University of Texas Health Science Center, San Antonio, TX DISCLOSURES: MKS declares that she has no competing interests. // Acknowledgements: Dr Maureen K. Sheehan would like to gratefully acknowledge Dr Dawn M. Barnes and Dr Gilbert R. Upchurch, the previous contributors to this monograph. DISCLOSURES: DMB and GRU declare that they have no competing interests. // Peer Reviewers: Ross Naylor, MBBS Professor of Vascular Surgery Vascular Surgery Group, Division of Cardiovascular Sciences, Leicester Royal Infirmary, UK DISCLOSURES: RN declares that he has no competing interests. William Pearce, MD Chief of Division of Vascular Surgery Department of Surgery, Northwestern Memorial Hospital, Chicago, IL DISCLOSURES: WP declares that he has no competing interests.