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PY1-Oral cases

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COMMUNITY-ACQUIRED PNEUMONIA: Infection of the Lower Respiratory Tract
CAUSES
Strep. Pneumonia Gram
(+)
H. influenzae/M.
catarrhalis
lancet-shaped diplococcus
in chains
Gram (-) coccobacillus,
encapsulated
Mycoplasma pneumonia /
Legionella pneumophilia
Chlamydophila pneumonia
Gram (-) bacilli
Atypical’ bacteria with no cell wall
SYMPTOMS
Abrupt onset
common in smokers,
in young adults with prodrome of
-Fever with chills
COPD, alcoholics
fever, chills, headache, sore
-Chest pain
throat, malaise, dry cough
-Productive “rust(mucoid)
colored" cough
-Transmitted by aerosolization,
-Malaise
incubation period of 2-4 weeks
-Sre throat
-Rhinorrhea
-Shortness of breath
GOAL OF THERAPY
RISK FACTORS
 Assess severity of pneumonia to determine General
appropriate initial treatment setting
-Altered levels of consciousness (sleep, intoxication

Relieve symptoms such as cough, pleuritic
chest pain, sputum production and/or
dyspnea
(alcohol or other CNS depressants), neurological diseases
(stroke or seizure, dementia)

Prevent morbidity
cough/gag reflexes, endotracheal intubation, chest tubes

Prevent mortality in nonpalliative patients
-Impaired cellular or humoral immunity malnourished

Prevent transmission

Prevent recurrence
elderly, patients on chronic corticosteroids or other
immunosuppressed, HIV/AIDS, cancer
-Impaired mechanical defenses smoking, impaired
-Chronic debilitating diseases asthma, CHF, COPD,
cerebrovascular disease, chronic kidney disease, liver
disease
DIAGNOSTIC TEST
CURB 65:
C – Confusion (1pt)
U—(BUN) >7mmol/L (1pt)
R—RR > or = 30/min (1pt)
ICU
B—BP, <90/ ≤60 (1pt)
Age ≥ 65 yrs (1pt)
PSI:
LAB RESULTS
CURB Scores:
- 0-1: outpatient
- 2: inpatient
- 3: inpatient –
Chest X-Ray
Right lobe unilateral or bilateral infiltrates
or
Interstitial pattern with Atypical’ bacteria
- 4 and 5: ICU
Gram stain/Cultures
Adequate specimen:
>25 Neutrophils
Slow onset, then high fever, CNS effects like H/A,
obtundation, seizures, malaise, non-productive
cough, hyponatremia
-recent travel, age, chronic illness
Risk Factors for PRSP (penicillin resistant strep
pneumonia)
-Age >65 years
-Beta-lactam therapy within the past 3 months
-Alcoholism
- Immune-suppressive illness or medications
-Multiple medical comorbid conditions
-Exposure to a child in a day care center
-Score of 90 or less = outpatient
-Score of >91+ = admit to hospital
Inpatient Treatment: Non-ICU
Give B-lactam + Macro/Doxy or Respiratory FQ x 510days
-FQ: Levofloxacin 750mg po daily or Moxifloxacin
400mg po daily
-B-lactam (oral): Azithromycin 500mg x 1 day, then
250mg po daily
-B-lactam (IV):
Cefuroxime 750-1500mg IV q8h
Ceftriaxone 1-2g IV daily
Cefotaxime 1-2g IV q6h
Ampicillin 1-2g IV q6h
Ertapenem 1g IV q24h
Outpatient No Risk Factors/Co-morbidities
Empiric Therapy:
-Macrolides or Doxycycline:
-Azithromycin 500mg x 1, then 250mg daily
-Clarithromycin 500mg po bid or clarithromycin ER
100mg po daily
-Doxycycline 200mg po once, then 100mg po bid or
1000mg po bid
-Duration of therapy: 5-7 days
MONITORING
Effectiveness
-Decrease fever to 37.7 (give acetaminophen)
-Decrease Sx (cough, fatigue chills etc...)
-CURB score to <1
-HR ≤100BPM
-RR ≤24 BPM
-Systolic BP ≥ 90mmHG
-Arterial O2 sat ≥90%
-Normal LOC
<10 Epithelial cells per LPF
TREATMENT OPTIONS
Inpatient Treatment: ICU
Give B-lactam IV + Macro or Respiratory FQ x5-14
days
-B-lactam (IV):
Cefuroxime 750-1500mg IV q8h
Ceftriaxone 1-2g IV daily
Cefotaxime 1-2g IV q6h
Ampicillin 1-2g IV q6h
Ertapenem 1g IV q24h
-Macrolides: azithromycin 500mg x1 day then 250mg
po daily, or clarithromycin 500mg po bid, clarithro-ER
1000mg po daily
-FQ: Levofloxacin 750mg po daily or Moxifloxacin
400mg po daily
Outpatient with Risk Factors/ Co-morbidities
Empiric therapy: B-lactam + macrolide (or doxy as
alternative) OR Resp FQ
-Levofloxacin 750mg po daily
-Moxifloxacin 400mg po daily
-B-lactam PO: Amoxicillin 1g po BID-TID, or
Amox/clav 875/125mg po BID
-B-lactam IV: Cefuroxime 750-1500mg IV q8h, or
Ceftriaxone 1-2g IV daily
-Macrolide: Azithromycin 500mg PO/IV daily
-Duration of therapy: 5-7 days
If MRSA -> Add Vancomycin or Linezolids to current
therapy
-Vancomycin 25-30mg/kg IV once then 15mg/kg IV
q8-12h
-Linezolid 600mg PO/IV BID for at least 14 days
If Pseudomonas: Pip/Tazo, meropenem, or cefepime
NON-PHARM
-Rest
-Smoking cessation
-Avoid second-hand smoke
-Fluids to stay hydrated
-Cold compress if they have fever
Safety
*side effects of all recommended Rx- name them- presence – time frame (anytime)
*allergic reactions to recommend Rx (hives, rash, anaphylaxis – time frame (anytime)
URINARY TRACT INFECTION: infection of the upper or lower urinary tract
CAUSES
mostly E.Coli
Others: staphylococcus, klebsiella pneumoniae
SYMPTOMS
GOALS OF THERAPY
DIAGNOSTIC TEST
Cystitis: Lower UTI
Asymptomatic
Polynephritis: Upper UTI
-Relieve symptoms in acute
• Urinalysis
-do not treat
infection
(Bladder)
(Kidney)
• Urine culture
Voided urine with ≥10^8 cfu/L of -All lower UTI symptoms
-Frequency of urination
• Sensitivity
-Prevent complications of
same
-Urgency of urination
-CVA tenderness
untreated acute infection
organism +/- pyuria and no S/S
(costovertebral angle
-Dysuria (pain upon
-Prevent recurrent infection
-No Treatment in Elderly
tenderness)
urination)
-Prevent pyelonephritis in
-Flank pain
-Nocturia (peeing at night)
pregnancy
-Rigors
-Fever (rare)
-Fever, chills
RISK FACTORS
LAB RESULTS
1.Obstruction
5.Men
Macroscopic urinalysis
Tumors, strictures, stones, etc This prevents
Anal intercourse, benign prostatic hyperplasia
– Appearance Cloudy, turbid, smelly
flushing of urine
(BPH), congenital disorders
– Specific gravity May be a bit dilute
 BPH causes increased prostate gland
– pH > 4.5 to 8.5
2.Post-void Residual
 Congenital is a structural abnormality
– Protein Common finding
Neurological diseases, drugs, etc Unable to
– Glucose Should be (-)
empty bladder
6.Other
– Nitrite (+) if gram (-) bacteria
-Pregnancy, immunosuppression
– Leukocyte (+) if pyuria is present
3.Vesico-Ureteral Reflux
-Diabetes  Sugar spills into urine, providing
Congenital malformation and pregnancies 
nutrients to bacteria
Microscopic urinalysis
Reflux causes urine from bladder to go back to
-Menopause
– WBC > 5/hpf (or >10/mm3)
ureter and kidney
 Estrogen protects women against UTIs;
– Casts (+) if pyelonephritis
therefore, lose estrogen = risk increases
– RBC trauma, catheter
4.Women
 Decrease in lactobacilli results in a less acidic
Rectum is close to vagina  Introduces organisms vagina
– Epithelial cells <25 cells/hpf
into vagina and bladder
– Bacteria (+)
Treatment
Cystitis Uncomplicated
Mild to Moderate Complicated UTI
Mild to Moderate Pyelonephritis
-1st Line: SMX/TMP po x 3 days, or TMP po x 3
-1st Line: Nitrofurantoin PO x 7-10 days, or
-1st Line: Ciprofloxacin or levofloxacin PO x 7-14
days, or nitrofurantoin po x 3 days, or fosfomycin
SMX/TMP x 7-10 days, or TMP x 7-10 days, or
days
tromethamine po x 1 dose
ciprofloxacin or levofloxacin x 7-10 days
-2nd Line: Amoxicillin/Clavulanate PO x 10-14 days,
nd
-2 Line: Ciprofloxacin, norfloxacin, or
-2nd Line: Amox/Clav PO x 7-10 days, or cephalexin or SMX/TMP PO x 10-14 days, or Trimethoprim x
levofloxacin po x 3 days, or cephalexin po x 7 days PO x 7-10 days, or cefexime PO x 7-10 days
10-14 days
Recurrent Infection
NON-PHARM
- Increase water intake
- avoid spermicidals
-avoid scented products
-Keep area clean and dry
-Avoid wearing thigh pants
-wear cotton based underwear
MONITORING
Effectiveness
-Reduce/Eliminate Sx (pain, frequent
urination, dysuria, nocturia)
-Cure Infection
-Reduce/eliminate fever if present
-Adherence to med- not skipping dose,
finishing course- presence – (timeframe
within a few days)
Safety
*side effects of all recommended Rxname them- presence – time frame
(anytime)
*allergic reactions to recommend Rx
(hives, rash, anaphylaxis – time frame
(anytime)
C. DIFFICILE (DIARRHEA)
CAUSES
-Diarrhea associated with C. difficile (CDI) Gram (+), anaerobic, spore forming bacilli
- Antibiotics associated diarrhea (ADD)
GOAL OF THERAPY
SYMPTOMS
ADD
-Prevent mortality
Severe CDI
-Diarrhea: mild, 3-4
-Cure infection
Pseudomembranous Colitis (PMC)
stools/day
-Alleviate symptoms
-Red, inflamed mucosa and areas
-Afebrile,
-Prevent complications
with white exudate (pseudo
-No abdominal pain
-Minimize risk of recurrence
membranes) on large intestine
-WBC
is
not
elevated
-Prevent transmission of CDI
-Underneath pseudo membranes =
-Minimize unnecessary use of
Necrosis of mucosal surface
antimicrobials
-Patient education
Toxic Megacolon
Minimize adverse drug reactions
Dilation of colon; bowels expands
and perforates
CDI
-Presence of diarrhea (3 liquid or loose stools/day)
-Fever, rigors, chills, malaise
-Increased HR and RR, Decreased BP
-Watery diarrhea (mild to profuse, distinct smell)
-Blood may present
-Loss of appetite, nausea, abdominal pain, tenderness,
cramping
-Severe infection?  Pseudomembranous colitis,
colonic ileus, toxic megacolon
-Increased SCr (this can be used as a marker)
Lab Values
-Increased WBC count
o Severe: > than 15e109 L
o Fulminant: > than 50e109 L
-Increased neutrophils, band neutrophils (immature
neutrophils), lactate, leukocytes,
-Decreased albumin
RISK FACTORS
- Advanced age
- Prolonged hospital stays
- GI surgery and inflammatory bowel
diseases
Immunosuppression, organ transplant,
hemotherapy, CKD, exposure to infant carrier or
infected adult Gastric acid suppression
-Clavulanate: stimulates bowel motility
-Erythromycin: stimulates bowels
-Broad-spectrum antibiotics: alters intestinal
flora (Clindamycin, Cephalosporins,
Fluoroquinolones)
CLASSIFICATION OF CDI
Non-severe
-WBC = or < 15
SCr < 133 umol/L
Severe
-WBC > 15
-SCr > or = 133 umol/L
-Pseudomembranous colitis
Fulminant
Hypotension, shock, ileus, or megacolon present
-Acute= <14 days in duration
-Chronic= >28 days in duration
-Recurrence of CDI symptoms between 2 and 8
weeks
Treatment
Non-Severe Disease:
-Vancomycin 125 mg QID PO × 10 days
or
-Fidaxomicin 200 mg BID PO × 10 days
or (if vancomycin or fidaxomicin unavailable)
-Metronidazole 500 mg TID PO × 10 days
Severe Disease:
-Vancomycin 125 mg QID PO × 10 days
or
-Fidaxomicin 200 mg BID PO × 10 days
Fulminant Disease:
-Vancomycin 500 mg QID PO + Metronidazole 500 mg Q8H IV + (if
ileus present) Vancomycin 500 mg in 100 mL saline Q6H PR as
retention enema
DIAGNOSTIC TEST
Bristol Stool chart
(type 6/7) unless ileus is suspected
*Important to test only if clinical presentation is
consistent with CDI to avoid detecting colonization
Nucleic acid amplication test (NAAT) aka PCR
-Looks for c.diff toxin gene
-Limitation: cannot detect between active infection
vs. Asymptomatic carrier
-Should not be used alone for diagnosis
Toxin A + B enzyme immunoassay (EIA): can be
used as standalone test for dx
Glutamate dehydrogenase (GDH) screening
-Detects for GDH (enzyme produced by c.diff)
-Does not detect toxins, do not use alone
Treatment for Recurrence
1st Recurrence:
-If metronidazole used for initial episode: Use Vancomycin 125 mg QID PO × 10 days
-If vancomycin used for initial episode: Use Fidaxomicin 200 mg BID PO × 10 days
-If vancomycin standard regimen used for initial episode: Use Vancomycin tapered and
pulsed regimen:
-Vancomycin 125 mg QID PO × 10–14 days
-Vancomycin 125 mg BID PO × 7 days
-Vancomycin 125 mg once daily PO × 7 days
-Vancomycin 125 mg Q2–3 days PO × 2–8 wk
2nd Recurrence:
-Vancomycin tapered and pulsed regimen
-Vancomycin 125 mg QID PO × 10 days; followed by rifaximin 400 mg TID PO × 20 days
or
-Fidaxomicin 200 mg BID PO × 10 days
3rd Recurrence: As per second recurrence or Fecal microbiota transplantation
NON-PHARM
MONITORING
Effectiveness
*(reduction of symptoms -name them) Decrease and time frame
*Adherence to med- not skipping dose, finishing course- presence – (timeframe within a few days)
-Antimicrobial stewardship
-Contact precautions (use gloves and gowns)
-Hand hygiene: must be with soap and water; hand
sanitizer is not effective against C. difficile spores
-drink lots of fluids (electrolytes)
Safety
*side effects of all recommended Rx- name them- presence – time frame (anytime)
*allergic reactions to recommend Rx (hives, rash, anaphylaxis – time frame (anytime)
*Specific CDI monitoring points
• GI: abdominal exam (daily)
– bowel sounds, pain, distension
– Bristol Stool Chart: stool frequency/volume/consistency
– Diarrhea should be resolving within 4-6 days
• Hydration status (daily)
• Labs (daily)
– CBC with differential, electrolytes (Na, K, Cl), SCr
• Imaging: AXR or CT (if concern of ileus, megacolon,
perforation)
VULVOVAGINITIS:
Goals of therapy
Vulvovaginal candidiasis (VVC;
yeast infection)
-Candida albicans (80-90%)
-C. glabrata (5-10%)
-C. tropicalus (5%)
-C. krusei (1%)
Sx -itchy, Curd like, clumpy,
white colour, erythema,
swelling, minimal or no
odour, dysuria, dyspareunia
excoriation, fissures
pH: <4.5
MD referral: 1st time; other
CAUSES
Bacterial vaginosis (BV)
Trichomoniasis
Gardnerella vaginalis or
anaerobes (mycoplasmas)
SYMPTOMS
Sx-thin, copious amounts,
grey or milky color, fishy
smell
-pH:5-6
MD referral
Partner: no treatment
necessary
Trichomonas vaginalis
Sx -itchy, strong fishy smell, Frothy
Yellow green or off-white colour
-pH: ≥6
MD referral
-Partner: treat, even without screening or
asymptomatic (avoid intercourse during treatment)
complications
Partner: treat only if
symptomatic
CLASSIFICATION
RISK FACTORS
NON-PHARM
Often absent
•More common if sexually
active
•Current or recent antibiotic use
•Hormonal (pregnancy, oral
contraceptives, hormone
replacement)
•Poorly controlled diabetes
•Immuno-compromised
(corticosteroids, chemotherapy,
HIV)
-Good genital hygiene
-Avoid warm, moist
environments
-Avoid mechanical and
chemical trauma
-Apply cold compress to area
MONITORING
Effectiveness
*(reduction of symptoms -name them) Decrease and
time frame
*Adherence to med- not skipping dose, finishing
course- presence – (timeframe within a few days)
Safety
*side effects of all recommended Rx- name thempresence – time frame (anytime)
*allergic reactions to recommend Rx (hives, rash,
anaphylaxis – time frame (anytime)
SPORT INJURIES
Goals of therapy
CAUSES
-Trauma
-Overuse of specific body parts (e.g.,
muscles or joints)
-Environmental (e.g., heat stroke)
SYMPTOMS


Pain
Swelling
RISK FACTORS



Improper technique
Lack of poorly fitting
protective equipment
Training errors
Acute injuries:
ligament sprains and muscle strains
-Sudden trauma
-More likely to occur in contact
sports
Chronic injuries:
Achilles tendonitis, bursitis, plantar
fasciitis, shin splints, tennis elbow, stress
fractures
 Repetitive movements
 “Terrible toos”--too fast, too
frequent, too far
NON-PHARM
- Movement (if safe and possible)
- Compression
- Elevation
ESA
E: indicated for condition, most effective/drug choice,
optimal dose, freq, duration, route, interaction
affecting effectiveness
MONITORING
Effectiveness
*(reduction of symptoms -name them) Decrease and time
frame
S: no contraindications, adverse drug reactions, DTP,
interaction affecting safety,
*Adherence to med- not skipping dose, finishing coursepresence – (timeframe within a few days)
A: complexity of regimen, product availability, pt
preferences (cost, regimen, dosage form, lifestyle,
challenges)
Safety
*side effects of all recommended Rx- name them- presence –
time frame (anytime)
*allergic reactions to recommend Rx (hives, rash, anaphylaxis –
time frame (anytime)
LOW BACK PAIN and NECK PAIN
CAUSES
Back Pain:
-mechanical
-sprain/strain of muscles
-deconditioning of musculature (exacerbated by
age and use related deterioration of structures)
-poor posture
-inciting events (physical labour accidental injury
such as workplace, motor vehicle)
Goals of therapy
Neck Pain:
Motor vehicle collisions
Assess RED Flags:
(Low Back Pain):
-Cauda equina syndrome
(LBP):
(Neck Pain):
SYMPTOMS
Low Back Pain:
-Pain often present in back, buttock
and legs
- Radiating pain down legs may be
present
-Can be intermittent or constant but
constant is quite rare
-Often relieved by flexion or extension
-Back (worst pain in back/buttock) or
leg dominant (worst pain in legs -thigh,
calf, ankle, foot)
-Symptoms may be absent or lessened
in first 24 hours
Assess YELLOW Flags:
(Neck Pain)
-Duration of work absence
Neck pain
-Pain and stiffness
sometimes extends to head,
chest, shoulders, and arms.
-Decreased range of motion
-Headache, dizziness
-Self-reported unexplained high-intensity pain and disability
-Cancer
-Spinal fracture or
compression fracture
-Autoimmune cause
-Infectious cause
-Neurological
-Infection
-Fracture
-Tumor
-inflammation
-Prior history of absenteeism
-High levels of self-reported functional
disability
-Self-report of extreme pain and constant
pain in multiple body areas
-History of prolonged sick listing after
previous injuries
RISK FACTORS
Neck pain
- Female
-Younger age
-Prior history of neck pain
-Rear collision
-Stationary vehicle
-Severity of collision
-Not being at fault
-Monotonous work
-Litigation (Australia legislation change reduced
LBP Pregnancy:
-Overweight
-Previous history of back pain
-Hormonal changes
-Weight gain
-Catastrophizing or a belief that pain and activity may
potentially be disabling
-Depression, anxiety or signs of post-traumatic stress
(consider the Patient Health Questionnaire for Depression
and Anxiety
-Passive coping strategies, possibly manifesting as
expectation of passive treatment rather than a belief that
active participation will help (consider using the Pain SelfEfficacy Questionnaire
-Avoidance of movement
-History of previous musculoskeletal pain
CLASSIFICATION OF PAIN
Neck pain
Low Back Pain:
•Acute: (within hours) 1-4 weeks
• Acute: < 4 weeks
• Subacute: 4-12 weeks
• Subacute: 4-12 weeks
• Chronic: 6 months or more
• Chronic: >12 weeks
incidence compared to historical numbers)
CORE tool (history)
- Clinically organized relevant exam
- Tool to help with Assessment and
management of patients with back pain/
neck pain and triage patients to
appropriate specialist intervention when
needed
NON-PHARM
-
Encourage patient to continue or resume
activity and work as soon as tolerated
Avoid unnecessary bedrest
Encourage Exercise daily (E.g., walks,
stretching) as tolerated
Can use heating pad or cooling pad to help
with pain relief
DIAGNOSTIC TEST
Physical Exam (back pain):
Physical Exam (neck pain):
- Observation of gait
- Document range of motion
-Standing
and associate pain in the
-Lying
neck as baseline
-Sitting
-Observe gait
-Sensation
-Standing
-Sitting
-Radicular testing
-Upper motor neuron screen
Diagnostic Imaging:
-Use only when red flags are present *
-MRI or CT scan for low back pain
-Plain radiographs for neck pain lasting
for more than a few weeks
ESA
E: indicated for condition, most effective/drug
choice, optimal dose, freq, duration, route,
interaction affecting effectiveness
MONITORING
Effectiveness
*(reduction of symptoms -name them) Decrease and
time frame
S: no contraindications, adverse drug reactions,
DTP, interaction affecting safety,
*Adherence to med- not skipping dose, finishing
course- presence – (timeframe within a few days)
-
Can massage the area
Can try yoga
Relaxation therapy
Cognitive behavioral therapy
Mindfulness-based stress reduction
Maintain healthy body weight (low back pain)
A: complexity of regimen, product availability, pt
preferences (cost, regimen, dosage form, lifestyle,
challenges)
Safety
*side effects of all recommended Rx- name thempresence – time frame (anytime)
*allergic reactions to recommend Rx (hives, rash,
anaphylaxis – time frame (anytime)
Pregnancy:
- Water based exercises (LBP)
GOUT and HYPERURICEMIA
Goals of therapy
-Terminate the acute attack of
arthritis
-Prevent recurrence
-Prevent or reverse complications
-Treat associated disorders
CAUSES
-MSU crystal deposits (needle
shaped crystals) in joints, soft
tissues (cartilage, tendon, bursa)
Hyperuricemia (urate levels
>360umol/L in females and
>420umol/L in males)
SYMPTOMS
-Abrupt onset
-Extreme pain
-Inflammation of joint during the
night or early morning
-Tenderness, warmth, swelling, and
redness
-Max severity within 12-24hrs
-Usually asymmetrical
-Commonly affects lower limb;
higher frequency in upper limb
involvement in women
Chronic Gout
Tophi in polyarticular joint
RISK FACTORS
-Asymptomatic hyperuricemia (urate levels
>360umol/L in females and >420umol/L in males)
-Male and post-menopausal women
-Alcohol (excessive consumption)
-Obesity
-Men at higher risk vs. women
-High purine diet and drugs
->65 years old
-Genetics
LAB RESULTS
Urate lowering therapy target:
Drugs:
-Cyclosporine
-Cytotoxic chemotherapy
-Diuretics (Thiazide and loop)
-Ethambutol
-Interferon + ribavirin
-Levodopa
-Niacin (nicotinic acid)
-Pyrazinamide
-Salicylates, low-dose
-Tacrolimus
-teriparatids
Comorbidities:
-Atherosclerosis
-Diabetes (T2DM)
-Hyperlipidemia
-HTN
-Urolithiasis history
-Chronic kidney disease
DIAGNOSTIC TEST
Gout diagnosis calculator: https://www.mdcalc.com/acute-gout-diagnosis-rule
- <360umol/L for most patients
- <300umol/L if presence of tophi or chronic arthropathy (once resolved,
target <360umol/L)
Indications for chronic urate lowering therapy (hyperuricemia tx):
Diagnosis of gout + one of the following below:
- Tophi
- Frequent gout flares (2 or more per year)
- CKD ≥ Stage 2 (GFR 60-89mL/min)
- Past urolithiasis (kidney stones)
- Early age of onset (< 40 y.o) + very high serum urate (475umol/L)
Treatment
Acute Gout
-1st Line: NSAIDs, Colchicine, or oral
corticosteroid
-Colchicine: 1.2 mg PO at first sign of
flare, then 0.6 mg 1 h later; start
prophylactic therapy 12 h later
-Prednisone: 0.5 mg/kg daily × 5 days
PO; Effective dose range: 20–50
mg/day
-Naproxen: 750 mg STAT, then 500
mg BID × 4–5 days PO
Definitive diagnosis (Gold standard): Identification of intracellular monosodium
urate crystals in synovial fluid aspirate
ACR/EULAR classification criteria:
-Score of 8 or more is considered diagnostic for gout
-3-part criteria:
 Clinical presentation (sx, timing, presence of tophi)
 Labs (crystal in joint aspiration, urate >360umol/L)
 Imaging (Xray/CT findings)
Ultrasonography
-Can detect MSU crystals
-First choice during acute attack
Hyperuricemia (Urate lowering tx)
-1st Line:
Allopurinol: Starting dose: 100 mg daily PO
Usual: 300 mg daily PO titrated to urate levels;
maximum: 800 mg daily PO; To improve
tolerability, divide doses >300 mg to 2–3
times/day
-Alternative:
Febuxostat: Starting dose: 40 mg daily PO;
may increase to 80 mg daily after 2 wk if
serum uric acid levels remain above 360
µmol/L
Prophylaxis START after Initiating Urate-Lowering
Therapy
-Initiation of uric acid lowering therapy can precipitate
attacks due to mobilization of tophi
Anti-inflammatory medications
-1st Line:
Colchicine: 0.6 mg once to twice daily PO x 3 – 6
months
Alternatives:
-Prednisone: < or = 10mg/d x 3 - 6 months
-Indomethacin: 25 mg po BID x 3 - 6 months
-Naproxen: 250mg po BID x 3 - 6 months
Goals of
Therapy
-Decrease recurrence of gout attacks
-Prevent the formulation of tophi
-Prevention of progressive joint
damage
-Improve/maintain quality of life
NON-PHARM
-Topical ice application
- Weight loss (maintain healthy BMI)
-Exercise regularly
-Quit smoking
-Stay hydrated, drink lots of fluids
-Avoid organ meats high in protein
such as liver, and kidneys
-avoid foods and beverages high in
fructose and corn syrup
-encourage low fat or non-fat dairy
products and vegetables
-Use assisted devices (eg: cane)
ESA
E: indicated for condition, most effective/drug
choice, optimal dose, freq, duration, route,
interaction affecting effectiveness
MONITORING
Effectiveness
*(reduction of symptoms -name them) Decrease and
time frame
S: no contraindications, adverse drug
reactions, DTP, interaction affecting safety,
*Adherence to med- not skipping dose, finishing
course- presence – (timeframe within a few days)
A: complexity of regimen, product availability,
pt preferences (cost, regimen, dosage form,
lifestyle, challenges)
Safety
*side effects of all recommended Rx- name thempresence – time frame (anytime)
OSTEOARTHRITIS
CAUSES
SYMPTOMS
RISK FACTORS
Wearing out of hyaline articular cartilage








Joint pain
Stiffness (<30 minutes, does not feel as bad in morning)
Decreased range of motion
Increasing age
Increased BMI
Genetics
Poor diet
Injury, malalignment, abnormal loading of joints
*allergic reactions to recommend Rx (hives, rash,
anaphylaxis – time frame (anytime)
DIAGNOSTIC
TEST
X-Ray findings:
 White -> bone (due to calcium)
 Grey/black -> cartilage (due to no calcium)
 In OA:
Clusters of white -> indicates cartilage destroyed and bone is touching and grinding against another bone
Result: progressive fibrillation occurs due to loss of cartilage (cannot grow cartilage back)
LAB RESULTS
THOUGH PROCESS
-Look at symptoms
-Identify cause of disease
-Identify risk factors
-BMI, past injury?
-Check vital signs
-Check lab value
-Write down goals of therapy CTC
-Underline desired outcome
-Find DTP based on NESA
-Check if any contraindications
-Check for drug interactions
-Check patient allergies
-Check patient preferences and
concerns
-Check social history
-Make recommendation
write full regimen (rationale for
recommendation based on ESA)
-Find alternative (pros and cons)
write full regimen
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
-Write Monitoring
NON-PHARM
 Education
 Exercise (land-based
aerobic, land-based
resistance, aquatic)
 Weight management
 Physiotherapy
RHEUMATOID ARTHRITIS
CAUSES
Autoimmune disorder
ESA
E: indicated for condition,
most effective/drug choice,
optimal dose, freq, duration,
route, interaction affecting
effectiveness
MONITORING
Effectiveness
*(reduction of symptoms name them) Decrease and
time frame
S: no contraindications,
adverse drug reactions, DTP,
interaction affecting safety,
*Adherence to med- not
skipping dose, finishing
course- presence – (timeframe
within a few days)
A: complexity of regimen,
product availability, pt
preferences (cost, regimen,
dosage form, lifestyle,
challenges)
Safety
*side effects of all
recommended Rx- name
them- presence – time frame
(anytime)
*allergic reactions to
recommend Rx (hives, rash,
anaphylaxis – time frame
(anytime)
SYMPTOMS





Joint pain during activity/rest
Morning stiffness (>30-60min)
Pain (worst in morning)
Inflammation, swelling, warmth
Systemic symptoms are common
RISK FACTORS





Female
Smoking
Alcohol, coffee, oral contraceptives use
Genetics
Low socioeconomic status
VITAL SIGNS
DIAGNOSTIC
TEST
Diagnostic Criteria for RA
Suspect RA If 6 points or more
Points Joint involvement
0
1 medium/large joint
1
2-10 medium joints
2
1-3 small joints
3
4-10 small joints
Serology
Negative RF and ANA
Acute-phase
reactant
Normal ESR
and CRP
Elevated ESR
and CRP
Duration
<6 weeks
>6 weeks
Low positive RF and
ANA
High positive RF and
ANA
5
>10 joints (at least 1
small joint)
THOUGH PROCESS
NON-PHARM
-Look at symptoms
-application of cold
-Identify cause of disease
compress
-Identify risk factors
-educate patient about
-Check vital signs
disease
-Check table 3 CTC, for poor
-emotional and
prognostics? (for combo therapy) psychological support
-Check lab value, CrCl?
-physical rehabilitation
-Active TB? Need for Vaccine?
-encourage physical activity
-Write down goals of therapy CTC (cardiorespiratory fitness,
-Underline desired outcome
flexibility, muscle strength,
-Find DTP based on NESA
ESA
E: indicated for condition,
most effective/drug choice,
optimal dose, freq, duration,
route, interaction affecting
effectiveness
S: no contraindications,
adverse drug reactions, DTP,
interaction affecting safety,
MONITORING
Effectiveness
*(reduction of symptoms name them) Decrease and
time frame
*Adherence to med- not
skipping dose, finishing
course- presence – (timeframe
within a few days)
Safety
-Check if any contraindications
-Check for drug interactions
-Check patient allergies
-Check patient preferences and
concerns
-Check social history
-Make recommendation
write full regimen (rationale for
recommendation based on ESA)
-Find alternative (pros and cons)
write full regimen
-Does patient need folic acid or
adjunct therapy?
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
-Write Monitoring
and neuromotor
performance)
A: complexity of regimen,
product availability, pt
preferences (cost, regimen,
dosage form, lifestyle,
challenges)
*side effects of all
recommended Rx- name
them- presence – time frame
(anytime)
*allergic reactions to
recommend Rx (hives, rash,
anaphylaxis – time frame
(anytime)
ACNE
CAUSES
SYMPTOMS
RISK FACTORS


Multifactorial inflammatory disease centered on the pilosebaceous gland of the skin
Follicular hyperkeratinization, microbial colonization with Cutibacterium acnes (aka propionibacterium
acnes), sebum production, inflammatory mechanism involving both innate and acquire immunity
 Impaired skin barrier
 Genetic
 Diet
 Hormones
Comedonal Acne
Mild:
Moderate:
Severe:
 Only presence of
 Open or closed
 Several Inflammatory  Multiple nodules,
open of closed
comedones present
lesions (papules and
cysts, and scarring
comedones
pustules)
 Few papules and
 Numerous papules
pustules
 May contain a few
and pustules
nodules
 Conglobate acne




Stress
Pre-menstrual flares
Use of oil products
Local friction


Improper cleansing of hair and skin
Drug induced: oral contraceptives (especially with androgenic progestins e.g., levonorgestrel),
androgens, barbiturates, corticosteroids, haloperidol, lithium, phenytoin, bromides, iodides
 Diet (controversial): high glycemic load diets may exacerbate acne; dairy ingestion is weakly associated
with acne
THOUGH PROCESS
NON-PHARM
ESA
MONITORING
-Look at symptoms
E: indicated for condition,
Effectiveness
-Identify cause of disease
-avoid picking, squeezing or most effective/drug choice,
*(reduction of symptoms -Identify risk factors
scratching inflammatory
optimal dose, freq, duration,
name them) Decrease and
-Check vital signs
lesions as it delays healing
route, interaction affecting
time frame
-Check lab value
and promotes scarring
effectiveness
-Write down goals of therapy CTC -use fragrance-free
*Adherence to med- not
-Underline desired outcome
moisturizers
S: no contraindications,
skipping dose, finishing
-Find DTP based on NESA
-reduce psychological
adverse drug reactions, DTP,
course- presence – (timeframe
-Check if any contraindications
stress (e.g., meditation)
interaction affecting safety,
within a few days)
-Check contraceptive ingredient
-find ways to help boost
on CPS if contains
self-esteem
A: complexity of regimen,
Safety
-Check for drug interactions
-wear sunscreen or hat
product availability, pt
*side effects of all
-Check patient allergies
when under sunlight for a
preferences (cost, regimen,
recommended Rx- name
-Check patient preferences and
long period of time
dosage form, lifestyle,
them- presence – time frame
concerns
-patients should wash no
challenges)
(anytime)
-Check social history
more than twice daily with
-Make recommendation
mild soap or soapless
*allergic reactions to
write full regimen (rationale for
cleanser
recommend Rx (hives, rash,
recommendation based on ESA)
anaphylaxis – time frame
-Find alternative (pros and cons)
(anytime)
write full regimen
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
-Write Monitoring
ROSACEA
CAUSES






Immune dysfunction
Ultraviolet radiation and temperature extremes
Vascular hyperreactivity/neurovascular degeneration --> flushing
Microorganism
Genetics
TRPs (transient receptor potential channels) are activated and release substance P & CGRP -->
pain/edema, vasodilation
SYMPTOMS
 Flushing
 Persistent erythema (Centrofacial—forhead, nose, chin, cheeks)
 Telangiectasia
 Papules/pustules
 Phymatous changes
 Ocular manifestations
RISK FACTORS Epidemiology:
 Women
 Ages between 30-50yo
SUBTYPES OF
ROSACEA
Triggers
 Fair skinned northern European descent
 Affect people who blush/flush easily
 People with sensitive skin
1. Erythematotelangiectactic 2. Papulopustular
rosacea (Vascular phase)
rosacea
(inflammatory phase)
 Persistent central
 Small papules and
erythema; prolonged
pustules, no
flushing
comedones
 Telangiectasia

Burning, stinging,
 Roughness (scaling)
flushing
 Burning and stinging
 Episodes of facial
edema may be
present








3. Phymatous rosacea
 Marked skin
thickening and
irregular
nodularities of nose,
chin, ears, forehead,
or eyelids
 Rhinophyma –
sebaceous gland
hyperplasia &
fibrous connective
tissue
4. Ocular rosacea
 Water, blood-shot
eyes
 Dry eyes, Irritation,
Foreign body
sensation
 Photophobia
Blepharitis
 Conjunctivitis
 Scleritis
 Keratitis
 Eyelid irregularities
 inflammation
Sunlight
Heat
Hot beverages
Spicy foods, vinegar
Alcohol
Emotional stress
Use of astringents (alcohol or acetone-based products)
Drugs: CCBs, niacin, nicotinic acid, nitrates, topical corticosteroids, sildenafil, opioid analgesics,
amiodarone, topical steroids, nasal steroids, high doses of VitB6 and VitB12
THOUGH PROCESS
NON-PHARM
ESA
MONITORING
-Look at symptoms
E: indicated for condition,
Effectiveness
-Identify cause of disease
-avoid triggers
most effective/drug choice, *(reduction of symptoms -Identify risk factors
-wear sunscreen (SPF 30 and optimal dose, freq, duration, name them) Decrease and
-Check vital signs
above)
route, interaction affecting
time frame
-Check lab value
-general skin care for
effectiveness
-Write down goals of therapy CTC
sensitive skin (Fragrance*Adherence to med- not
-Underline desired outcome
free moisturizers, non-soap S: no contraindications,
skipping dose, finishing
-Find DTP based on NESA
cleansers, avoid astringents) adverse drug reactions, DTP, course- presence –
-Check if any contraindications
-use of camouflage makeup interaction affecting safety, (timeframe within a few
-Check for drug interactions
-wear hat when exposed to
days)
-Check patient allergies
sunlight for a long period of A: complexity of regimen,
-Check patient preferences and
time
product availability, pt
Safety
concerns
-stress reduction
preferences (cost, regimen,
-Check social history
-Make recommendation
write full regimen (rationale for
recommendation based on ESA)
-Find alternative (pros and cons)
write full regimen
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
-Write Monitoring
dosage form, lifestyle,
challenges)
*side effects of all
recommended Rx- name
them- presence – time frame
(anytime)
*allergic reactions to
recommend Rx (hives, rash,
anaphylaxis – time frame
(anytime)
PSORIASIS
CAUSES

T cells migrate to the epidermal and dermal areas of skin and cause excess production of cytokines and
proinflammatory factors
SYMPTOMS
RISK
FACTORS

Grey scaly plaques on skin
Exogenous triggers
 Climate (cold, dry, sunny)
 Stress, infections, trauma,
smoking, obesity, alcohol
Drugs







DIAGNOSTIC Body Surface Area (BSA):
 Mild= <5% BSA
TEST
 Moderate= 5-10% BSA
 Severe= >10% BSA
THOUGH PROCESS
NON-PHARM
-Look at symptoms
Phototherapy with a 308 nm
-Identify cause of disease
excimer laser (if available) may
-Identify risk factors
be considered in scalp
-Check vital signs, BMI?
psoriasis that is resistant to
-Check lab value
topical therapies
-Write down goals of therapy -smoking cessation
CTC
-encourage to maintain a
-Underline desired outcome
healthy BMI/ diet
-Find DTP based on NESA
-limit alcohol consumption
-Check if any
-reduce stress (e.g., try
contraindications
meditation)
-Check for drug interactions
-use an emollient**
-Check patient allergies
-Check patient preferences
and concerns
-Check social history
-Make recommendation
write full regimen (rationale
for recommendation based
on ESA)
Lithium
Beta blockers
Anti-malarials
NSAIDs
ACE-inhibitors
Abrupt
withdrawal of
corticosteroids
Benzodiazepines,
tetracycline,
interferon-alpha
Comorbid conditions
 Depression
 CV disease
 Hypertension
 Obesity
 Psoriatic arthritis
 Inflammatory bowel disease
 Multiple sclerosis
Psoriasis Area Severity Index (PASI)50/70/100
ESA
E: indicated for condition,
most effective/drug choice,
optimal dose, freq, duration,
route, interaction affecting
effectiveness
MONITORING
Effectiveness
*(reduction of symptoms name them) Decrease and
time frame
S: no contraindications,
adverse drug reactions, DTP,
interaction affecting safety,
*Adherence to med- not
skipping dose, finishing
course- presence – (timeframe
within a few days)
A: complexity of regimen,
product availability, pt
preferences (cost, regimen,
dosage form, lifestyle,
challenges)
Safety
*side effects of all
recommended Rx- name
them- presence – time frame
(anytime)
*allergic reactions to
recommend Rx (hives, rash,
anaphylaxis – time frame
(anytime)
-Find alternative (pros and
cons)
write full regimen
-MOA of prescribed Rx
(generic, class) and
recommended drugs
-Write Non-pharm
-Write Monitoring
ATOPIC DERMATITIS

Abnormality of epidermal structure and function impairs skin barrier function, causing deficiency in
SYMPTOMS


ceramides (lipids) and filaggrin (proteins)
Inflammatory skin condition characterized by pruritus, erythema and scale
IgE associated but NOT defined as type 1 IgE-mediated reaction
RISK FACTORS




CAUSES
TYPES OF
ATOPIC
DERMATITIS
Age <5 years old
Family history of atopic dermatitis
Other atopic conditions
Environmental factors (high sugar diet, small family size, high household education level, living in an
urban setting)
Mild
Moderate
Severe
 Localized patches of dry skin
 Localized patches of dry skin
 >30% of BSA
 Erythema
 Infrequent itching
 Pruritus

THOUGH PROCESS
-Look at symptoms
- is quality of life affected?
-Identify cause of disease
-Identify risk factors
-Check vital signs
-Check lab value
-Write down goals of therapy CTC
-Underline desired outcome
-Find DTP based on NESA
-Check if any contraindications
-Check for drug interactions
-Check patient allergies
-Check patient preferences and
concerns
-Check social history
-Make recommendation
write full regimen (rationale for
recommendation based on ESA)
-Find alternative (pros and cons)
write full regimen
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
-Write Monitoring
Some impact on sleep, daily
activities
NON-PHARM
 Keep fingernails short
 Bathe once a day to
remove crusts,
irritants, and allergens;
immediately following
with moisturizers
 Use warm water, not
cold or hot
 Wet-wraps can be used
in significant flare-ups

Persistent pruritus, extensive
lichenification, crackling,
oozing, and altered
pigmentation

Major impact on sleep and daily
activities
ESA
E: indicated for condition,
most effective/drug choice,
optimal dose, freq, duration,
route, interaction affecting
effectiveness
MONITORING
Effectiveness
*(reduction of symptoms name them) Decrease and
time frame
S: no contraindications,
adverse drug reactions, DTP,
interaction affecting safety,
*Adherence to med- not
skipping dose, finishing
course- presence – (timeframe
within a few days)
A: complexity of regimen,
product availability, pt
preferences (cost, regimen,
dosage form, lifestyle,
challenges)
Safety
*side effects of all
recommended Rx- name
them- presence – time frame
(anytime)
*allergic reactions to
recommend Rx (hives, rash,
anaphylaxis – time frame
(anytime)
SCABIES AND LICE
CAUSES
Scabies and Lice exposure
SYMPTOMS
Head Lice:
 May be asymptomatic
 Wheals develop within 24hrs
 Lesions on scalp
 Pruritis
 Excoriations may be as visible as red papules
around the ears, face, and neck
 Itching may be delayed until sensitization
occurs after 4-6wks for patients without prior
infestation
 Generalized rash, conjunctivitis, cervical
lymphadenopathy
Body Lice:
 Lesions on flanks, waist, neck, and axillae
(trunk)
 Pruritis and skin reactions (parallel linear
excoriations, red marks)
Scabies:
 May take 4-6wks for symptoms to develop
 Erythematous papular rash, burrows
 Lesions are white-silvery linear or S-shaped burrows
 Inflammation, papules, vesicles, scales
 Intense itching 3-10wks later; particularly at night; itching can persist
for wks
Pubic Lice:
 Pruritis in pubic area
 Rust-colored specks on pubic hair
 Excoriations
 Bluish macules in the pubic area
 May also affect the eyelashes, eyebrows,
beard, or axillae
RISK FACTORS
Head Lice (prevalence):
 Children 3-12 yo
 Females > males
 More cases in August to November
 Affects all SES levels
 No causal relationship between hygiene and nutritional status
Body Lice:
 Poor hygiene
Pubic Lice:
 Most common in 15-40 yo
 May be associated with coexisting STIs
Head Lice:
Scabies:






Direct head-to-head/ hair-to-hair contact
Pets are not vectors for human head lice
Lice present on host’s scalp
Body lice:
TRANSMISSION



Highly contagious
Direct skin-to-skin contact
Can be present in web spaces of fingers, front of wrists, sides of hands
& feet, back of elbow, skin folds, underarms, breasts, groin, abdomen,
back (Rarely above neck)
Direct physical contact
Contact with infested clothing, bedding, etc
Lice present in the seams of clothing
Pubic Lice:
DIAGNOSTIC
TEST
THOUGH PROCESS

Physical contact, sexual exposure to an
infected person


Visual detection of lice, and nits
Scabies diagnosis should be made/confirmed by physician (dermatologist)
NON-PHARM
ESA
MONITORING
-Look at symptoms
-Identify cause of disease
-Identify risk factors
-Check vital signs
-Check lab value
-Write down goals of therapy CTC
-Underline desired outcome
-Find DTP based on NESA
-Check if any contraindications
-Check for drug interactions
-Check patient allergies
-Check patient preferences and
concerns
-Check social history
-Make recommendation
write full regimen (rationale for
recommendation based on ESA)
-Find alternative (pros and cons)
write full regimen
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
-Write Monitoring
-identify and examine
potential human contacts
-soak combs and brushes in
disinfectant solution (e.g.,
Lysol 2% for 1hr or rubbing
alcohol for 10-20mins) or in
hot water (at least 50C for 510 mins)
-use hot water cycle to wash
all clothing items, bedsheets,
pillowcases, towels, etc. of
infected person
-seal items in plastic bag for
2wks
-(Body lice) improve hygiene
-(pubic lice) if in eyelashes,
use white petrolatum
(vaseline) can be applied to
lashes 2-4 times daily for 10
days, remove lice and nits
with forceps or tweezers
-(pubic lice) refer to physician
for concurrent STIs
-(scabies) use cold compress
x20mins for severely itchy
areas
-(scabies) avoid body contact
with others until full
treatment cycle is completed
OTITIS MEDIA
CAUSES
SYMPTOMS






AOM:
Streptococcus pneumoniae (most common)
Viruses
H. influenzae
Moraxella catarhalis
Group A streptococci
Staph aureus
OME:
E: indicated for condition,
most effective/drug
choice, optimal dose, freq,
duration, route,
interaction affecting
effectiveness
Effectiveness
*(reduction of symptoms -name them) Decrease and
time frame
S: no contraindications,
adverse drug reactions,
DTP, interaction affecting
safety,
Safety
*side effects of all recommended Rx- name thempresence – time frame (anytime)
A: complexity of regimen,
product availability, pt
preferences (cost,
regimen, dosage form,
lifestyle, challenges)
*Adherence to med- not skipping dose, finishing
course- presence – (timeframe within a few days)
*allergic reactions to recommend Rx (hives, rash,
anaphylaxis – time frame (anytime)





Rapid onset
Otalgia (Ear tugging)
Otorrhea
Headache
Fever
RISK FACTORS
-Young age
-Allergies
- Daycare
-Second-hand smoke
- Immunodeficiency
-Pacifier use
Strategy for:
WATCHFUL
WAITING

 Hearing loss
 Tinnitus
 Vertigo
 Otalgia
 Irritability, difficulty sleeping
 Loss of appetite
 Vomiting, diarrhea
-Upper respiratory tract infections
- Family history of recurrent OM
- Craniofacial abnormalities
- Trisomy 21 (down syndrome)
- Short duration of breast feeding
-GERD
Close monitoring and follow-up:
Children >6mos, with unilateral AOM, mild
 If symptoms worsen or fail to improve after 48-72hrs,
symptoms (otalgia <48hrs, with temp (po) <39C)
follow up with MD visit, or start antibiotic Rx
 Children >24mos, with mild symptoms and
unilateral or bilateral AOM
DIAGNOSTIC
 Requires otoscopy
TEST
 Redness, inflammation, bulging tympanic membrane
 Opaque yellow tympanic membrane
 Impaired mobility of tympanic membrane
THOUGH PROCESS
NON-PHARM
ESA
MONITORING
-Look at symptoms
-don’t share pillowcases,
E: indicated for condition,
Effectiveness
-Identify cause of disease
and clean and wash
most effective/drug choice,
*(reduction of symptoms -Identify risk factors
infected person’s pillow
optimal dose, freq, duration,
name them) Decrease and
-Check vital signs
cases
route, interaction affecting
time frame
-Check lab value
-avoid loud noises; it can
effectiveness
-Write down goals of therapy CTC irritate ears
*Adherence to med- not
-Underline desired outcome
-Fever: cold compress,
S: no contraindications,
skipping dose, finishing
-Find DTP based on NESA
cooling fan, tepid bath
adverse drug reactions, DTP,
course- presence –
-Check if any contraindications
-get lots of rest
interaction affecting safety,
(timeframe within a few
-Check for drug interactions
-stay hydrated, drink lots of
days)
-Check patient allergies
fluids
A: complexity of regimen,
-Check patient preferences and
-warm facial
product availability, pt
Safety
concerns
packs/compresses
preferences (cost, regimen,
*side effects of all
-Check social history
-sleeping with the head of
dosage form, lifestyle,
recommended Rx- name
-Make recommendation
the bed elevated
challenges)
them- presence – time frame
(anytime)
write full regimen (rationale for
recommendation based on ESA)
-Find alternative (pros and cons)
write full regimen
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
-Write Monitoring
*allergic reactions to
recommend Rx (hives, rash,
anaphylaxis – time frame
(anytime)
SINUSITIS (Acute RHINOSINUSITIS in CTC)
CAUSES
SYMPTOMS
RISK FACTORS




















Acute:

Classification
Viruses (most common)
Strept pneumoniae
H. influenzae
Moraxella catarhalis
Staph aureus
Anaerobes (more likely in chronic infection)
Facial pain, pressure or fullness
Referred pain to ears, teeth
Headache
Purulent nasal discharge
Fever
Altered smell, taste
Halitosis
Cough
Cough and rhinorrhea are most common symptoms in children
Recent upper viral respiratory tract infection
Asthma
Allergic rhinitis, rhinitis medicamentosa
Smoking or second-hand smoke
Anatomy (e.g., deviated septum, turbinate deformity)
Viral:
<4wks
Chronic:
 Symptomatic > or = 12 wks
Recurrent:
 4 or more episodes per year


Symptoms rapidly peak, and
start to decline by the 3rd day,
ends in 1 wk
Will overall be improving even
if symptoms last over a week
Bacterial:


10 days or longer with no
improvement
Severe symptoms and high fever
(>39C) with purulent discharge or
facial pain 3-4 consecutive days at
start of illness
with complete resolution
between episodes
DIAGNOSTIC
TEST

NON-PHARM
-nasal saline irrigation or
steam inhalation may be
helpful
-avoid exacerbating factors
such as allergen exposure,
environmental toxins,
tobacco smoke
-rest
-stay hydrated, drink lots of
fluids
-hand washing is the best
way to reduce the spread of
viral infections
PHARYNGITIS



Symptoms start to improve, but
get worse by 10 days (“double
sickening”)
Differentiate between viral and bacterial based on symptom timeline
THOUGH PROCESS
-Look at symptoms, how long?
-Bacterial or viral ?
-give signs of referral?
-Identify cause of disease
-Identify risk factors
-Check vital signs
-Check lab value
-Write down goals of therapy CTC
-Underline desired outcome
-Find DTP based on NESA
-Check if any contraindications
-Check for drug interactions
-Check patient allergies
-Check patient preferences and
concerns
-Check social history
-Make recommendation
write full regimen (rationale for
recommendation based on ESA)
-Find alternative (pros and cons)
write full regimen
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
-Write Monitoring
CAUSES

Viruses (most common)
Streptococcus Pyogenes (Group A strep)*
Group C, G streptococci
ESA
E: indicated for condition,
most effective/drug choice,
optimal dose, freq,
duration, route, interaction
affecting effectiveness
S: no contraindications,
adverse drug reactions,
DTP, interaction affecting
safety,
A: complexity of regimen,
product availability, pt
preferences (cost, regimen,
dosage form, lifestyle,
challenges)
MONITORING
Effectiveness
*(reduction of symptoms -name
them) Decrease and time frame
*Adherence to med- not skipping
dose, finishing course- presence –
(timeframe within a few days)
Safety
*side effects of all recommended
Rx- name them- presence – time
frame (anytime)
*allergic reactions to recommend
Rx (hives, rash, anaphylaxis – time
frame (anytime)
SYMPTOMS
RISK FACTORS
Complications
DIAGNOSTIC
TEST
 Arcanobacterium hemolyticum
 N. Gonorrheae
 Corynebacterium diptheriae
 Fusobacterium necrophorum (Lemierre’s disease)
 Acute primary HIV infection
General:
Bacterial:
Absence of cough, odynophagia,
 Abrupt onset
pharyngeal/tonsilar erythema (+/ Sore throat, exudate
exudate), fever, palatal petechiae,
 Odynophagia
tender cervical adenopathy, scarlet
 Tonsillar swelling
fever, winter/spring presentation
 Palatal petechiae
Viral:
 Odynophagia, cough,
rhinorrhea, conjunctivitis,
hoarseness; diarrhea, rash
 Fever, chills
 Tender cervical adenopathy
 Malaise
 Headache
 Smoking, secondhand smoke
 Allergic rhinitis
 Seasonality (November to May)
 Behavioral risk factors (e.g., N. gonorrhea)
 Exposure to infected person within last two weeks (transmitted via airborne droplets)
Epidemiology:
 Kids 5-10 yo in winter/spring
 Uncommon if <3 yo
Infectious complications:
Postinfectious complications:





Peritonsillar or retropharyngeal abscess
Cervical lymphadenitis
Sinusitis
Otitis media
Mastoiditis






Acute rheumatic fever (autoimmune inflammatory
disorder)
glomerulonephritis
Throat culture
Rapid antigen detection test (RADT)
Testing not routinely recommended for children <3 yo
Modified Centor Score:



0-1 criteria: low risk (<3%), no testing
4 or more points (50%), test
CTC: If cumulative score is 3, 4 and more points, it increases likelihood that the patient has GAS
pharyngitis
THOUGH PROCESS
-Look at symptoms
-Modified centor test
-RADT (rapid antigen test)
sensitive
-culture (specific)
-Identify cause of disease
-Identify risk factors
-Check vital signs
-Check lab value
-Write goals of therapy CTC
-Underline desired outcome
-Find DTP based on NESA
-Check if any contraindications
-Check for drug interactions
-Check patient allergies
-Check patient preferences and
concerns
-Check social history
-Make recommendation
write full regimen (rationale for
based on ESA)
-Find alternative (pros and
cons)
write full regimen
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
NON-PHARM
-rest
-soft food diet
-stay hydrated, drink lots of
fluids
-handwashing is the best
way to reduce the spread of
viral infections
-fever: cooling fan, tepid
bath, cold compress on
forehead
ESA
E: indicated for condition,
most effective/drug choice,
optimal dose, freq, duration,
route, interaction affecting
effectiveness
MONITORING
Effectiveness
*(reduction of symptoms name them) Decrease and
time frame
S: no contraindications,
adverse drug reactions, DTP,
interaction affecting safety,
*Adherence to med- not
skipping dose, finishing
course- presence – (timeframe
within a few days)
A: complexity of regimen,
product availability, pt
preferences (cost, regimen,
dosage form, lifestyle,
challenges)
Safety
*side effects of all
recommended Rx- name
them- presence – time frame
(anytime)
*allergic reactions to
recommend Rx (hives, rash,
anaphylaxis – time frame
(anytime)
-Write Monitoring
CONJUNCTIVITIS
CAUSES
SYMPTOMS
RISK FACTORS
Conjunctivitis
 Airborne allergens contacting
eye
CLINICAL FINDINGS
itching
redness
discharge
Bacterial
Viral
 Staph aureus (common)
 Adenovirus (most common)
 Strep pneumoniae
 H. influenzae
 Moraxaella catarrhalis
VIRAL
BACTERIAL
ALLERGIC
minimal
minimal
severe
generalized
generalized
generalized
Profuse, serous
Moderate, mucopurulent Moderate, serous, mucoid
or purulent
Bacterial
 Exposure to virulent/unique bacterial strains
 Immunocompromised
 Diabetes
 Regular contact lens wearers
 Recent ocular surgery
VITAL SIGNS
DIAGNOSTIC
TEST
THOUGH PROCESS
-Look at symptoms
-Identify cause of disease
-Identify risk factors
-Check vital signs
-Check lab value
-Write down goals of therapy CTC
-Underline desired outcome
-Find DTP based on NESA
-Check if any contraindications
NON-PHARM
 Avoid contact lenses
until resolves
 Avoid makeup, smoke,
wind, and other
irritants
 Apply cold compresses
for allergic and viral
conjunctivitis;
ESA
E: indicated for condition,
most effective/drug choice,
optimal dose, freq, duration,
route, interaction affecting
effectiveness
S: no contraindications,
adverse drug reactions, DTP,
interaction affecting safety,
MONITORING
Effectiveness
*(reduction of symptoms name them) Decrease and
time frame
*Adherence to med- not
skipping dose, finishing
course- presence – (timeframe
within a few days)
-Check for drug interactions
-Check patient allergies
-Check patient preferences and
concerns
-Check social history
-Make recommendation
write full regimen (rationale for
recommendation based on ESA)
-Find alternative (pros and cons)
write full regimen
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
-Write Monitoring




warm compresses for
bacterial conjunctivitis
Practice lid hygiene for
blepharitis
(inflammation of
eyelids): Warm water
compresses to closed
eyelid for 5- 10 mins,
followed by gentle
scrubbing of lid
margins with warm
water. Repeat daily at
bedtime
Hand hygiene
Consider all shared
objects that may
contact infected eye(s)
(towel)
A: complexity of regimen,
product availability, pt
preferences (cost, regimen,
dosage form, lifestyle,
challenges)
Safety
*side effects of all
recommended Rx- name
them- presence – time frame
(anytime)
*allergic reactions to
recommend Rx (hives, rash,
anaphylaxis – time frame
(anytime)
ALLERGIC RHINITIS
CAUSES
SYMPTOMS
RISK FACTORS
Atopy: abnormal tendency to develop IgE response to innocuous and ubiquitous environmental allergens
 Often genetic
 Local immune response to allergen
Visible signs:
 Nasal congestion
 Persistent mouth breathing
 Nasal itch
 Rubbing at the nose or obvious transverse
 Rhinorrhea
nasal crease
 Sneezing
 Frequent sniffling or throat clearing
 Allergic conjunctivitis
 Allergic shiners (dark circles under the eyes
that are due to nasal congestion)
 Concomitant asthma
 Family history of atopy (asthma, allergic rhinitis, atopic dermatitis)
 Ethnic origin other than white European
 Heavy maternal smoking in first year of life
 Early introduction of food or formula
 No older siblings
 Allergen exposure (aeroallergens, food allergens, occupational allergens)
 Pollutants
 Higher SES
 Heavy alcohol consumption
Medical complications:
Complications
DIAGNOSTIC
TEST







Headaches
Cough
Ocular symptoms (itchy watery, red, swollen eyes)
Otitis media with effusion
Nasal polyps
Recurrent URTI
AR is an independent risk factor for developing asthma
Skin Testing:
 Preferred over serum IgE testing, unless conditions exist that make it unsatisfactory (e.g., widespread
skin disease or inability to stop antihistamine therapy)
 Primary method, more sensitive
 See procedure in lecture notes*
THOUGH PROCESS
NON-PHARM
ESA
MONITORING
-Look at symptoms
E: indicated for condition,
Effectiveness
-Identify cause of disease
-allergen avoidance
most effective/drug choice,
*(reduction of symptoms -Identify risk factors
(pollen, animal dander,
optimal dose, freq, duration,
name them) Decrease and
-Check vital signs
dust mites, mould)
route, interaction affecting
time frame
-Check lab value
-saline irrigation
effectiveness
-Write down goals of therapy CTC -cold or warm compress to
*Adherence to med- not
-Underline desired outcome
help reduce conjunctivitis
S: no contraindications,
skipping dose, finishing
-Find DTP based on NESA
symptoms
adverse drug reactions, DTP,
course- presence – (timeframe
-Check if any contraindications
interaction affecting safety,
within a few days)
-Check for drug interactions
-Check patient allergies
A: complexity of regimen,
Safety
-Check patient preferences and
product availability, pt
*side effects of all
concerns
preferences (cost, regimen,
recommended Rx- name
-Check social history
dosage form, lifestyle,
them- presence – time frame
-Make recommendation
challenges)
(anytime)
write full regimen (rationale for
recommendation based on ESA)
-Find alternative (pros and cons)
write full regimen
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
-Write Monitoring
*allergic reactions to
recommend Rx (hives, rash,
anaphylaxis – time frame
(anytime)
OTITIS EXTERNA
CAUSES
Impacted Cerumen
– Acute (< 3 weeks)
– Chronic (>= 3 mo)
– Malignant otitis externa
SYMPTOMS
– Fullness, hearing loss, tinnitus, itchiness
– Pain should not be present
RISK FACTORS
– Anatomic variations in ear canal (excess narrowing,
degree of
curvature, ear hair)
– Overproduction of cerumen
– Migration failure (Aging changes cerumen production
and skin
changes in the ear)
– Foreign objects placed in the ear (Q-tips) including
hearing aids
– History of prior impaction
– Older age
2 most common organisms:
 Pseudomonas Aeruginosa (20-60%)
 Staph Aureus (10-70%)
Rare:
 Fungal infection: Otomycosis, Aspergillus,
Candida Albicans
 Otitis Externa
 Pain (otalgia) ranges from mild to severe—
exacerbated by the movement of lobe, acute
onset within 48hrs, unilateral in 90% cases
 Itching/pruritis
 Ear fullness
 Headache
 Discharge (otorrhea)
 Swollen ear canal
 Loss of hearing
 Too little cerumen—cerumen provides
antibacterial action by physically protecting the
canal and maintaining a low pH
 Too much cerumen can lead to maceration and
occlusion
 Moisture (swimming, bathing, water sports,
increased humidity) macerates underlying skin and
raises pH
 Trauma to the external auditory canal (fingernails,
cotton-swabs, foreign objects)
 Use of objects occluding the auditory canal
 Chronic derm conditions
 Hearing aids
 Narrow, hairy ear canal

Age: high incidence in children 7-12 yo; rates
decline after 50
– Rash in ear or ear infection suspected
– History of ear surgery or tubes in ear
– Foreign object in ear
– Suspected burst ear drum:
REFERRAL
• Bleeding/discharge from ear
• Dizziness
• Pain
• Ringing sound
• Hearing loss
DIAGNOSTIC
 Based on clinical findings, history, and duration
TEST
 Otoscopy to distinguish between OM vs. OE
 Rule out malignant OE, AOM, derm conditions affecting the ear (eczema, seborrhea), sensitization from
otic medications
THOUGH PROCESS
NON-PHARM
ESA
MONITORING
-Look at symptoms
E: indicated for condition,
Effectiveness
-Identify cause of disease
-avoid trauma (cotton
most effective/drug choice,
*(reduction of symptoms -Identify risk factors
swabs, hair pins) in ear
optimal dose, freq, duration,
name them) Decrease and
-Check vital signs
canal
route, interaction affecting
time frame
-Check lab value
-avoid getting water into
effectiveness
-Write down goals of therapy CTC the ear canal
*Adherence to med- not
-Underline desired outcome
-use acidifying drops
S: no contraindications,
skipping dose, finishing
-Find DTP based on NESA
before or after swimming
adverse drug reactions, DTP,
course- presence – (timeframe
-Check if any contraindications
-examine hearing aids for
interaction affecting safety,
within a few days)
-Check for drug interactions
proper fit
-check if any ototoxicity drugs?
A: complexity of regimen,
Safety
-Check patient allergies
product availability, pt
*side effects of all
-Check patient preferences and
preferences (cost, regimen,
recommended Rx- name
concerns
dosage form, lifestyle,
them- presence – time frame
-Check social history
challenges)
(anytime)
-Make recommendation
write full regimen (rationale for
*allergic reactions to
recommendation based on ESA)
recommend Rx (hives, rash,
-Find alternative (pros and cons)
anaphylaxis – time frame
write full regimen
(anytime)
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
-Write Monitoring
DRY EYE DISEASE
CAUSES
SYMPTOMS
RISK FACTORS













Hyperosmolarity of tear film damages ocular surface by causing inflammation
Instability and dysfunction of tear film
Dry, scratchy, sandy feeling
Foreign body sensation
Pain and soreness
Increased blinking
Eye fatigue
Redness
Photosensitivity
Older age
Female
Postmenopausal estrogen therapy
Asian
VITAL SIGNS
DIAGNOSTIC
TEST
Aqueous Tear Flow (Schirmer Test)
o Normal: >15mm in 5 minutes
Tear Breakup Time (TBUT)
o Normal: >10 seconds for 1st dry spot to appear after blinking
THOUGH PROCESS
-Look at symptoms
-Identify cause of disease
-Identify risk factors
-Check vital signs
-Check lab value
-Write down goals of therapy CTC
-Underline desired outcome
-Find DTP based on NESA
-Check if any contraindications
-Check for drug interactions
-Check patient allergies
-Check patient preferences and
concerns
-Check social history
-Make recommendation
NON-PHARM
ESA
Environmental
E: indicated for condition,
 Avoid smoking or staying in most effective/drug choice,
smoky rooms
optimal dose, freq, duration,
 Avoid air drafts (e.g.,
route, interaction affecting
ceiling fans)
effectiveness





Wear sunglasses when
outdoors
Use humidifiers
Use moisture chamber
glasses
Wear ski or swim goggles
(± moistened gauze)
Use cool, moist
compresses for temporary
relief
Lifestyle
MONITORING
Effectiveness
*(reduction of symptoms name them) Decrease and
time frame
S: no contraindications,
adverse drug reactions, DTP,
interaction affecting safety,
*Adherence to med- not
skipping dose, finishing
course- presence – (timeframe
within a few days)
A: complexity of regimen,
product availability, pt
preferences (cost, regimen,
dosage form, lifestyle,
challenges)
Safety
*side effects of all
recommended Rx- name
them- presence – time frame
(anytime)
write full regimen (rationale for
recommendation based on ESA)
-Find alternative (pros and cons)
write full regimen
-MOA of prescribed Rx (generic,
class) and recommended drugs
-Write Non-pharm
-Write Monitoring



Screen time: decrease
screen time; take regular
breaks; lower computer
screen to below eye level;
make a conscious effort to
blink more often
Increase fluid intake
Increase sleep
*allergic reactions to
recommend Rx (hives, rash,
anaphylaxis – time frame
(anytime)
Punctal occlusion
Punctal plugs
 Temporary—usually
collagen-based; absorb in
1–16 weeks
 Permanent—usually
silicone-based
 Heat or electrocautery
(permanent)
GLAUCOMA
CAUSES
CLASSIFICATION
DIAGNOSTIC TEST
Group of ocular diseases associated with:
• elevated intraocular pressure (IOP)
• thinning of retinal nerve fibre and macular ganglion layer
• optic disk cupping & peripheral vision loss
Open-angle glaucoma
Angle-closure Glaucoma
Optic neuropathy characterized
• Closure of the angle between the
by progressive visual
iris and cornea,
field loss, usually associated with obstructing the outflow of aqueous
elevated intraocular
humor
pressure (IOP)
• About 1/3 of all glaucoma cases
• About 2/3 of all glaucoma
cases
• Primarily through
•Comprehensive eye examination
comprehensive eye
urgently (Refer)
secondary/acquired glaucoma
examinations and IOP
measurements
- Chronic, often asymptomatic
SYMPTOMS
RISK FACTORS
-Progressive visual loss
-Elevated IOP
• Demographics:
– Older age
– Female
– African ancestry
• Family history
• Medical history:
– Diabetes, high blood pressure,
taking corticosteroids
• Prior eye injury or surgery (e.g.
cataract surgery)
• Increased IOP
– Not always the case, some
with normal IOP will have
glaucoma and some with high
IOP never develop glaucoma
-Usually asymptomatic in early
disease
-Can lead to permanent blindness
within 24 hours
pain, blurry vision,
halos around lights, headache, N/V
• Demographics:
– Older age
– Female
– East Asian ancestry
• Family history
• Other ocular factors
Prognosis includes:
– Some may have residual OAG
– Reoccurring angle-closure
glaucoma
– Progressive vision loss
– Resolution of acute attack and
successful long term
management
• Congenital defects
• Trauma, surgery, insult/infection
• Corticosteroid use
VITAL SIGNS
THOUGH PROCESS
-Look at symptoms
-Identify cause of disease
-Identify risk factors
-Check vital signs
-Check lab value
-Write down goals of therapy CTC
-Underline desired outcome
-Find DTP based on NESA
-Check if any medical contraindications
-Check for drug interactions
-Check patient allergies
-Check patient preferences and concerns
-Check social history
-Make recommendation
write full regimen (rationale for
recommendation based on ESA)
-Find alternative (pros and cons)
NON-PHARM
– Aerobic exercise can
lower IOP modestly in
some
patients with glaucoma
-Patient Education
ESA
E: indicated for condition,
most effective/drug choice,
optimal dose, freq, duration,
route, interaction affecting
effectiveness
MONITORING
Effectiveness
*(reduction of
symptoms -name
them) Decrease and
time frame
S: no contraindications,
adverse drug reactions, DTP,
interaction affecting safety,
*Adherence to mednot skipping dose,
finishing coursepresence –
(timeframe within a
few days)
A: complexity of regimen,
product availability, pt
preferences (cost, regimen,
dosage form, lifestyle,
challenges)
Safety
*side effects of all
recommended Rxname them-
write full regimen
-MOA of prescribed Rx (generic, class) and
recommended drugs
-Write Non-pharm
-Write Monitoring
VTE
PADUA score
https://www.mdcalc.com/padua-prediction-score-risk-vte#next-steps
presence – time
frame (anytime)
*allergic reactions to
recommend Rx
(hives, rash,
anaphylaxis – time
frame (anytime)
(Medical patient only, not for surgery)
SYMPTOMS
Deep Vein Thrombosis:
- pain and/or tenderness
- swelling
- warm to touch
- change in color
Pulmonary Embolism:
- SOB
- Increased RR
- Chest pain
- Cough
 Increased HR
Abnormalities of surfaces in
contact with blood
- Vascular injury/trauma
- Major surgery (orthopedic)
- Valvular heart disease
- Heart valve replacement
- Atherosclerosis
- Central venous catheters
- Previous DVT/PE
RISK FACTORS
Abnormalities of Blood
Flow
- Immobility (bed
rest, paralysis,
travel)
- Left ventricular
dysfunction (i.e.,
heart failure)
- Atrial fibrillation
- Venous obstruction
(tumor, obesity,
pregnancy)
Abnormalities of Clotting
components
- Protein S or C deficiency
- ATIII deficiency
- Factor V Leiden mutation
- Antiphospholipid antibody
syndrome
- Homocystenemia
- Malignancy
- Increased estrogen
- Pregnancy
DIAGNOSTIC TEST
POSSIBLE THERAPIES
Start ONE of
- IV UFH---(use if renal impairment
present, Heparin Induced
Thrombocytopenia)
- SC LMWH—renally cleared, don’t
use in low CrCL, less AEs, more
cost effective
- SC fondaparinux
- SC UFH (weight-based)
Start Warfarin on the same day
Continue UFH/LMWH/FONDA x 5
days (min) and until INR > 2 x 48 hrs.
Usual dose: 0.5–6 mg daily PO
Adjust dose to maintain INR 2–3;
higher doses may be necessary in
some patients.
***CHECK FOR INTERACTIONS***
Duration of Therapy:
Provoked aka “idiopathic with
known cause” (reversible cause) x 3
months
Irreversible provoked cause—treat
as unprovoked
Unprovoked:
NON-PHARM
ESA
E: indicated for condition,
most effective/drug choice,
optimal dose, freq, duration,
route, interaction affecting
effectiveness
S: no contraindications,
adverse drug reactions, DTP,
interaction affecting safety,
A: complexity of regimen,
product availability, pt
preferences (cost, regimen,
dosage form, lifestyle,
challenges)
MONITORING
Effectiveness
*(reduction of symptoms name them) Decrease and
time frame
Monitor:
- Baseline INR daily until
stabilized INR 2-3 and
Baseline CBC while on
UFH/LMWH/FONDA
*Adherence to med- not
skipping dose, finishing
course- presence – (timeframe
within a few days)
Safety
*side effects of all
recommended Rx- name
them- presence – time frame
(anytime)
*allergic reactions to
recommend Rx (hives, rash,
anaphylaxis – time frame
(anytime)



Proximal DVT/PE (first or
recurrence) --> extended
duration
Isolated distal DVT (first
episode) x 3 months
Isolated distal DVT
(recurrence) --> extended
duration
VTE prophylaxis
PADUA score
https://www.mdcalc.com/padua-prediction-score-risk-vte#next-steps
(Medical patient only, not for surgery)
Caprini score
https://www.mdcalc.com/caprini-score-venous-thromboembolism-2005
(surgery pt only) don’t use for orthopedic surgery considered high risk surgery
RISK FACTORS
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