Chronic Pulmonary Infection Dr Tom Fardon Respiratory SpR Diagnosis? • • • • • Shadow on CXR Weight loss Persistent sputum production Chest pain Increasing shortness of breath Differential Diagnosis • Lung Cancer – Not unreasonable • • • • Intrapulmonary abscess Empyema Bronchiectasis Cystic Fibrosis Intrapulmonary Abscess • • • • • • Indolent presentation Weight loss common Lethargy, tiredness, weakness Cough ± sputum High mortality if not treated Usually a preceding illness of some sort Preceding Illnesses • Pneumonia • Aspiration pneumonia – Vomiting – Lowered conscious level – Pharyngeal pouch • Poor host immune response – Hypogammaglobulinaemia Pathogens • Bacteria – Streptococcus – Staphylococcus (Particularly post ‘flu) – E-Coli – Gram Negatives • Fungi – Aspergillus Empyema Empyema • Pus in the pleural space • 57 % of all patients with pneumonia develop pleural fluid • Remainder are “Primary Empyema”, usually iatrogenic • High mortality – As high as severe pneumonia – > 20 % of all patients with empyema die Progression of Effusion to Empyema • Simple Parapneumonic Effusion – Clear fluid – pH > 7.2 – LDH < 1000 – Glucose > 2.2 • Complicated Parapneumonic Effusion – pH < 7.2 – LDH > 1000 – Glucose < 2.2 – Requires Chest Tube Drainage • Emyema – Frank pus – No other tests required – Requires Chest Tube Drainage Bacteriology • Aerobic organisms most frequently • Gram Positive – Strep Milleri – Staph Aureus • Usually post operative, or nosocmial • Immunocomprimised • Gram Negatives – E-Coli – Pseudomonas – Haemophilus Influenzae – Kelbsiellae • Anaerobes in 13 % of cases – Usually in severe pneumonia, or poor dental hygiene Diagnosis • Clinical suspicion –The slow to resolve pneumonia –Don’t forget the lateral chest film • CXR –Persisting effusion, particularly if loculations visible • USS –The preferred investigation –Simple, bedside test –Targetted sampling • CT –Differentiation between Empyema and Abscess CXR • Some obvious • Not always this large • Look for D sign • As always, better xrays increase sensitivity, and specificity CXR - D Sign Lateral CXR • Particularly useful in small retrodiaphragmatic collections • Not straightforward in ICU USS USS in Empyema CT Examination of Pleural Space Empyema CT Use USS or CT to position the drain site Insertion of a Surgical Drain QuickTime™ and a YUV420 codec decompressor are needed to see this picture. QuickTime™ and a YUV420 codec decompressor are needed to see this picture. QuickTime™ and a YUV420 codec decompressor are needed to see this picture. QuickTime™ and a YUV420 codec decompressor are needed to see this picture. Trocar Introduction QuickTime™ and a YUV420 codec decompressor are needed to see this picture. QuickTime™ and a YUV420 codec decompressor are needed to see this picture. Insertion of a Seldinger Drain QuickTime™ and a YUV420 codec decompressor are needed to see this picture. Insertion of a Seldinger Drain QuickTime™ and a YUV420 codec decompressor are needed to see this picture. Other Treatment • IV antibiotics – Broad spectrum – Co-amoxyclav initially • Oral antibiotics – Directed towards cultured bacteria – At least 14 days Summary • Empyema is bad, and best avoided • Detection of complicated pleural effusion requires sampling of the effusion • Ultrasound guidance is preferred, but not always needed – “Any body cavity can be reached with a green needle and a good strong arm” • Small bore seldinger type drains are preferred initially Treatment Options • • • • Stop smoking ‘Flu vaccine Pneumococcal vaccine Reactive antibiotics – Send sputum sample – Give antibiotics appropriate to most recent positive culture Treatment • When colonised with persistent bacteria – Prophylactic antibiotics – Nebulised colomycin – Pulsed IV abx – Alternating oral antibiotics Anti-inflammatory Treatment • Low dose macrolide antibiotics have been shown to reduce exacerbation rates in bronchiectasis – Clarithromycin 250 mg OD Prognosis • Recurrent infection • Abscesses and empyema • Colonisation Cystic Fibrosis • Congenital cause of bronchiectasis • And much more CF Incidence, Prevalence and Survival • Carrier rate of 1 in 25 • Incidence of 1 in 2,500 live births • By 2002 the number of adult patients exceeded the number of children • Carrier screening may influence numbers (Cunningham & Marshall 1998) • Those born in the 1990’s have a predicted survival into the 40’s Tayside Caseload (annual report 4/00 - 3/01) • • • • 36 patients registered 3 patients on active transplant list 3 patients not suitable for transplant 2 deaths Case Study • Diagnosed at 10 months with steatorrhea and LRTI • Stable until 13 when she required increasingly frequent IV’s • Pregnancy 1996 - TOP @ 16 weeks • Since 1998 she has suffered more frequent exacerbations and now requires IV’s monthly • • • • • • • Oxygen dependent Abnormal liver function Occasional episodes of DIOS Button gastrostomy inserted Transplant assessment Dec 2000 Overnight BiPAP from June 2001 Difficulty in controlling pain and nausea • Bi-lateral lung transplant Sept 2001 • June 2006 - severe pneumonia • Admitted to ICU • Large blood clot extracted from right main bronchus – Organising pneumonia • Still an in patient in ward 3 • Colonised with 3 distinct varieties of pseudomonas and MRSA • Ongoing IV antibiotics Specialities Involved • • • • • • • Respiratory Gastro-Intestinal Obs & Gynae GP/DN Surgery Transplant team Child & Family Psychiatry • ICU • Anaesthesia Summary • Chronic infection can mimic malignancy • Chronic infection can have a similar prognosis if untreated • Have a high index of suspicion, particularly when simple infection is not clearing