Family Medicine

Every diagnosis, screening guideline, medication, procedure, classification system, immunization schedule, and management strategy across the full lifespan — in one place.

01 Scope of Family Medicine

Family medicine is the only specialty defined by breadth rather than organ system, disease category, or patient age. A family physician manages undifferentiated illness across the entire lifespan — newborn through geriatric — in ambulatory, inpatient, and procedural settings. The scope includes preventive care and screening, chronic disease management (hypertension, diabetes, dyslipidemia, COPD, heart failure), acute care (infections, injuries, abdominal pain), mental and behavioral health (depression, anxiety, ADHD, substance use), musculoskeletal medicine, women's health (contraception, prenatal, menopause), pediatrics, geriatrics, dermatology, and office-based procedures. Family physicians provide approximately 200 million office visits annually in the United States — more than any other specialty.

The intellectual core of the specialty is the biopsychosocial model: disease is never purely biomedical. Social determinants (housing, food security, employment, insurance status), behavioral factors (tobacco, alcohol, physical activity, sleep), and psychological context (stress, trauma, family dynamics) are as clinically relevant as lab values. A comprehensive family medicine encounter integrates all three domains into every clinical decision.

The Four Pillars of Family Medicine Practice

PillarScopeKey Activities
Preventive CareAll ages — birth to deathImmunizations, cancer screening (USPSTF), cardiovascular risk assessment (ASCVD), well-child visits, annual wellness visits, counseling
Chronic DiseasePrimarily adult, increasing in adolescentsHypertension, DM2, dyslipidemia, COPD, asthma, CHF, CKD, thyroid disease, obesity — titrating medications, monitoring targets, preventing complications
Acute/Episodic CareAll agesURI, UTI, otitis, pharyngitis, skin infections, lacerations, fractures, abdominal pain triage, chest pain risk stratification
Behavioral HealthAll agesDepression, anxiety, ADHD, insomnia, substance use disorders, motivational interviewing, medication management, brief counseling
Photograph of a stethoscope, the primary diagnostic tool of the family physician
Figure 1 — The Stethoscope. The stethoscope remains the family physician's most versatile bedside tool, used in cardiac, pulmonary, abdominal, and vascular examinations across all age groups. Source: Wikimedia Commons. Public domain.

02 The Comprehensive Physical Exam

The family medicine physical exam adapts to context — a focused exam for an acute sore throat is fundamentally different from a comprehensive annual wellness exam. However, every family physician must be able to perform a complete head-to-toe examination and know the specific findings that trigger further workup or referral.

Vital Signs — The Fifth Vital Sign

Vital SignNormal Adult RangeCritical ThresholdsClinical Pearl
Blood Pressure< 120/80 mmHgElevated: 120-129/<80; Stage 1 HTN: 130-139/80-89; Stage 2: ≥140/90; Crisis: >180/120Confirm with repeated measurements on 2 separate occasions; use correct cuff size (bladder covers 80% of arm circumference)
Heart Rate60-100 bpmBradycardia <60; tachycardia >100; concern >150 at restIrregularly irregular = atrial fibrillation until proven otherwise
Respiratory Rate12-20/minTachypnea >20; bradypnea <12Count for a full 30 seconds; most commonly miscounted vital sign
Temperature36.1-37.2 °C (97-99 °F)Fever ≥38.0 °C (100.4 °F); hypothermia <35 °CElderly patients may be afebrile despite serious infection
O2 Saturation95-100%<92% on room air warrants urgent evaluation; COPD patients may have lower baselines (88-92%)Falsely normal in CO poisoning; falsely low with nail polish, poor perfusion, or dark skin pigmentation
Pain (0-10)0Functional impairment threshold varies; trend matters more than single numberUse age-appropriate scales: Wong-Baker FACES for children 3-7, numeric for adults

BMI Classification

BMI (kg/m²)CategoryClinical Implication
< 18.5UnderweightScreen for eating disorders, malnutrition, malignancy, hyperthyroidism
18.5-24.9NormalStandard risk
25.0-29.9OverweightLifestyle counseling; screen for metabolic syndrome
30.0-34.9Obesity Class IIntensive behavioral intervention; consider pharmacotherapy
35.0-39.9Obesity Class IIPharmacotherapy + behavioral; bariatric surgery if comorbidities present
≥ 40.0Obesity Class III (severe)Bariatric surgery evaluation; high risk for OSA, DM2, CVD

Exam by System — Key Findings That Change Management

HEENT: Conjunctival pallor (anemia), scleral icterus (liver disease), thyromegaly or nodules (palpate with patient swallowing water — nodules >1 cm need ultrasound), tympanic membrane (red/bulging = AOM; retracted/dull = effusion; perforation), oropharynx (tonsillar exudate + fever + anterior cervical LAD + absence of cough = Centor 3-4, consider rapid strep).

Cardiovascular: Murmur grading (I-VI scale; grade III+ or any diastolic murmur warrants echocardiogram), irregular rhythm (ECG to rule out AFib), JVD (right heart failure), carotid bruits (consider duplex ultrasound if symptomatic or high cardiovascular risk), peripheral edema grading (1+ to 4+).

Pulmonary: Wheezes (asthma, COPD, heart failure), crackles (pneumonia, pulmonary fibrosis, CHF), decreased breath sounds (effusion, pneumothorax), prolonged expiratory phase (obstruction). Assess respiratory effort, accessory muscle use, and ability to speak in full sentences.

Abdomen: Auscultate before palpation. Rebound tenderness and involuntary guarding = peritoneal irritation, requires urgent imaging. Murphy's sign (RUQ pain with inspiration during palpation = cholecystitis). McBurney's point tenderness (RLQ = appendicitis). Costovertebral angle tenderness (pyelonephritis). Hepatosplenomegaly requires workup.

Musculoskeletal: Range of motion testing (active then passive — pain with active but not passive = soft tissue; pain with both = intra-articular). Straight leg raise (radiculopathy: positive if reproduces leg pain at <60°). Drawer tests (ACL/PCL), McMurray's (meniscus), Phalen's/Tinel's (carpal tunnel).

Neurological: Cranial nerves II-XII, strength (0-5 scale), sensation (light touch, pinprick), deep tendon reflexes (0-4+ scale; 2+ = normal), cerebellar function (finger-to-nose, heel-to-shin, Romberg). Mini-Mental State Exam (MMSE) or Montreal Cognitive Assessment (MoCA) for cognitive screening in geriatric patients.

Physician performing a physical examination with a stethoscope
Figure 2 — Physical Examination. Systematic examination is the cornerstone of family medicine diagnosis, allowing pattern recognition that guides targeted workup. Source: Wikimedia Commons. Public domain.

03 Preventive Medicine Framework

Preventive care is the defining activity of family medicine. The US Preventive Services Task Force (USPSTF) issues evidence-graded recommendations (A, B, C, D, I) that drive screening and counseling decisions. Grade A/B recommendations are standard of care — most insurers cover them with no patient cost-sharing under the ACA. The USPSTF recommendation framework uses net benefit analysis: benefits of the intervention minus harms (false positives, overdiagnosis, procedural complications).

Core Screening Schedule — Adults

ConditionTestPopulationFrequencyUSPSTF Grade
HypertensionOffice BP measurementAdults ≥18Annual (or every 3-5 years if normal and <40)A
Diabetes (Type 2)Fasting glucose, A1C, or OGTTAdults 35-70 with overweight/obesityEvery 3 years if normalB
DyslipidemiaLipid panelMen ≥35, women ≥45 (earlier if risk factors)Every 5 years; more often if borderline or on therapyA/B
Colorectal cancerColonoscopy, FIT, Cologuard, flex sig, CT colonographyAdults 45-75Colonoscopy q10yr, FIT annually, Cologuard q1-3yrA
Breast cancerMammographyWomen 40-74Biennial (may be annual based on shared decision-making)B
Cervical cancerPap smear ± HPV co-testingWomen 21-65Pap q3yr (21-29); Pap+HPV q5yr or Pap q3yr (30-65)A
Lung cancerLow-dose CT chestAdults 50-80 with ≥20 pack-year hx, current or quit <15yrAnnualB
AAAAbdominal ultrasoundMen 65-75 who ever smokedOne-time screeningB
OsteoporosisDEXA scanWomen ≥65; postmenopausal <65 with risk factorsEvery 2 years if on therapy or high riskB
DepressionPHQ-2/PHQ-9All adults ≥18Annual or as indicatedB
Hepatitis CAnti-HCV antibodyAll adults 18-79One-time screeningB
HIVHIV 1/2 Ag/AbAll adults 15-65At least once; more if high riskA
The single most effective preventive intervention in primary care is tobacco cessation counseling + pharmacotherapy. Smoking causes 480,000 deaths/year in the US. NRT, bupropion, and varenicline all double quit rates. The 5 A's framework (Ask, Advise, Assess, Assist, Arrange) should be applied at every visit for every smoker.

Cardiovascular Risk Assessment

The Pooled Cohort Equations (PCE) estimate 10-year ASCVD risk using age, sex, race, total cholesterol, HDL, systolic BP, BP treatment status, diabetes, and smoking. Risk categories: low (<5%), borderline (5-7.4%), intermediate (7.5-19.9%), high (≥20%). The PCE drives statin initiation decisions per 2018 AHA/ACC cholesterol guidelines: high-intensity statin for ASCVD risk ≥20% or known ASCVD; moderate-intensity statin for 7.5-19.9% with risk enhancers; shared decision-making for 5-7.4%.

Clinician measuring blood pressure with an automated cuff on a patient's arm
Figure 3 — Blood Pressure Measurement. Accurate BP measurement requires correct cuff size, patient seated with back supported, feet flat, and arm at heart level. Measuring on 2 separate occasions is required for a hypertension diagnosis. Source: Wikimedia Commons. Public domain.

04 Hypertension Chronic

Hypertension affects 47% of US adults (~116 million) and is the leading modifiable risk factor for stroke, MI, heart failure, CKD, and aortic dissection. The 2017 ACC/AHA guidelines lowered the diagnostic threshold from 140/90 to 130/80 mmHg, instantly reclassifying ~31 million Americans as hypertensive.

Classification (2017 ACC/AHA)

CategorySystolic (mmHg)Diastolic (mmHg)Management
Normal<120<80Reassess annually
Elevated120-129<80Lifestyle modification; reassess in 3-6 months
Stage 1 HTN130-13980-89Lifestyle + pharmacotherapy if 10-yr ASCVD risk ≥10% or known CVD/DM/CKD
Stage 2 HTN≥140≥90Lifestyle + pharmacotherapy (two-drug combination if BP ≥20/10 above goal)
Hypertensive Crisis>180>120Urgency (no end-organ damage): oral meds, recheck in hours. Emergency (end-organ damage): IV meds, ICU

First-Line Antihypertensives

ClassExamples (Generic/Brand)MechanismPreferred WhenPearl
ACE InhibitorLisinopril (Prinivil, Zestril), enalapril (Vasotec), ramipril (Altace)Blocks ACE → ↓ angiotensin II → vasodilation + ↓ aldosteroneDM with proteinuria, CKD, HF with reduced EF, post-MIDry cough in 10-20%; angioedema rare but life-threatening; check K+ and Cr at 1-2 weeks; contraindicated in pregnancy
ARBLosartan (Cozaar), valsartan (Diovan), olmesartan (Benicar)Blocks AT1 receptor → same downstream effects as ACEI without coughACEI-intolerant (cough), same indications as ACEINever combine ARB + ACEI (ONTARGET trial: no benefit, more harm); check K+ and Cr
CCB (dihydropyridine)Amlodipine (Norvasc), nifedipine ER (Procardia XL)Blocks L-type Ca2+ channels in vascular smooth muscle → vasodilationBlack patients, elderly, angina, Raynaud's; no metabolic effectsPeripheral edema is dose-dependent (up to 30% at 10 mg); adding ACEI/ARB reduces edema
Thiazide/Thiazide-likeChlorthalidone 12.5-25 mg, hydrochlorothiazide (HCTZ) 25 mg, indapamide 1.25-2.5 mgInhibits NaCl cotransporter in DCT → ↓ intravascular volume, then sustained vasodilationBlack patients, elderly, osteoporosis (preserves bone Ca2+); first-line per ALLHATChlorthalidone is more potent and longer-acting than HCTZ; monitor K+, Na+, uric acid, glucose
The SPRINT trial (2015) showed that targeting SBP <120 (intensive) vs <140 (standard) reduced major cardiovascular events by 25% and all-cause mortality by 27% — but excluded diabetics and stroke patients. This trial was the primary driver behind the ACC/AHA threshold change. In practice, the target for most adults is <130/80; for frail elderly or patients with orthostatic symptoms, a more conservative <140/90 may be appropriate.

Resistant Hypertension

Defined as BP above goal despite 3 optimally dosed antihypertensives from different classes, one of which is a diuretic — or BP controlled on 4+ drugs. Prevalence: 10-15% of treated hypertensives. Workup: confirm adherence (pill counts, pharmacy fills), rule out white-coat HTN (24-hr ABPM or home BP monitoring), evaluate for secondary causes: primary aldosteronism (aldosterone/renin ratio >30 with aldosterone >15 ng/dL), renal artery stenosis (renal duplex or CTA), pheochromocytoma (24-hr urine metanephrines/catecholamines), obstructive sleep apnea (most common secondary cause — screen with Epworth or STOP-BANG), Cushing's syndrome (24-hr urine cortisol, overnight dexamethasone suppression). Fourth-line agent: spironolactone 25-50 mg daily (PATHWAY-2 trial: most effective add-on for resistant HTN).

Diagram showing the effects of high blood pressure on arterial walls and organ systems
Figure 4 — Hypertension Pathophysiology. Chronically elevated blood pressure damages arterial walls and contributes to end-organ damage in the heart, brain, kidneys, and retina. Source: Wikimedia Commons, by BruceBlaus. Licensed under CC BY 3.0.

05 Diabetes Mellitus Chronic

Type 2 diabetes mellitus (T2DM) affects 37 million Americans (~11% of the population). It is the leading cause of CKD, non-traumatic lower extremity amputation, and adult-onset blindness. Family physicians manage the majority of T2DM in the US. The ADA Standards of Care (2024) define diagnosis and management targets.

Diagnostic Criteria

TestNormalPrediabetesDiabetes
Fasting Plasma Glucose<100 mg/dL100-125 mg/dL (IFG)≥126 mg/dL
2-hr OGTT (75g)<140 mg/dL140-199 mg/dL (IGT)≥200 mg/dL
A1C<5.7%5.7-6.4%≥6.5%
Random Glucose + Symptoms≥200 mg/dL with polyuria, polydipsia, weight loss

Two abnormal tests are required for diagnosis in asymptomatic patients. A random glucose ≥200 with classic symptoms is diagnostic on a single test.

Pharmacotherapy — Stepwise Approach

Agent (Generic/Brand)MechanismA1C ReductionKey BenefitPearl
Metformin (Glucophage) 500-2000 mg/dayDecreases hepatic glucose production, increases insulin sensitivity1.0-1.5%First-line; weight-neutral; inexpensive; possible CV benefitHold if eGFR <30; risk of lactic acidosis overstated; GI side effects minimized with ER formulation; hold 48hr before iodinated contrast if eGFR <45
GLP-1 RA: semaglutide (Ozempic 0.25-2 mg/wk, Wegovy), liraglutide (Victoza 0.6-1.8 mg/day), dulaglutide (Trulicity)Incretin mimetic → glucose-dependent insulin secretion, ↓ glucagon, delays gastric emptying, ↓ appetite1.0-1.8%Weight loss (5-15%), CV mortality reduction (LEADER, SUSTAIN-6, SELECT trials)Contraindicated with personal/family hx of medullary thyroid cancer or MEN2; nausea common at initiation — start low, titrate slowly
SGLT2i: empagliflozin (Jardiance 10-25 mg), dapagliflozin (Farxiga 5-10 mg), canagliflozin (Invokana)Blocks glucose reabsorption in proximal tubule → glycosuria, natriuresis0.5-0.9%CV death reduction (EMPA-REG), HF hospitalization reduction, CKD progression slowed (CREDENCE, DAPA-CKD)Risk of genital mycotic infections (candidal); euglycemic DKA (rare, suspect in ill patient on SGLT2i); hold perioperatively
Sulfonylureas: glipizide (Glucotrol 5-20 mg), glimepiride (Amaryl 1-4 mg)Stimulates pancreatic beta-cell insulin secretion (ATP-sensitive K+ channels)1.0-1.5%Rapid onset, inexpensiveHypoglycemia risk (especially glyburide — avoid); weight gain; avoid in CKD (accumulation)
DPP-4i: sitagliptin (Januvia 100 mg), linagliptin (Tradjenta 5 mg)Inhibits DPP-4 → prolongs endogenous GLP-1/GIP0.5-0.8%Weight-neutral, well-tolerated, oralNo CV benefit; less effective than GLP-1 RA; do not combine with GLP-1 RA (redundant mechanism)
Insulin: basal (glargine/Lantus, detemir/Levemir, degludec/Tresiba), prandial (lispro/Humalog, aspart/NovoLog)Exogenous insulin replacement1.5-3.5%Most potent glucose lowering; essential for T1DM and late-stage T2DMStart basal 10 units or 0.1-0.2 U/kg/day; titrate by 2 units q3 days to fasting glucose target; hypoglycemia and weight gain are dose-limiting
ADA Treatment Algorithm (Simplified)

Step 1: Metformin + lifestyle for all T2DM. Step 2: If established ASCVD or high CV risk → add GLP-1 RA (with proven CV benefit) or SGLT2i. If HF or CKD → add SGLT2i (preferred) or GLP-1 RA. If neither → add agent based on need to minimize hypoglycemia (GLP-1 RA, SGLT2i, DPP-4i), need for weight loss (GLP-1 RA, SGLT2i), or cost (sulfonylurea, TZD). Step 3: Add basal insulin if A1C remains above target after dual/triple oral/injectable therapy. A1C target: <7% for most adults; <6.5% if safe and achievable for younger patients; <8% for frail elderly, limited life expectancy, or history of severe hypoglycemia.

Monitoring & Complications Screening

A1C: Every 3 months if not at goal, every 6 months if stable. Annual foot exam: Semmes-Weinstein 10g monofilament + vibration (128 Hz tuning fork) to screen for peripheral neuropathy; inspect for ulcers, deformity, calluses. Annual eye exam: Dilated fundoscopy or retinal photography for diabetic retinopathy (DR stages: none, mild NPDR, moderate NPDR, severe NPDR, PDR). Urine albumin-to-creatinine ratio (UACR): Annual; microalbuminuria = 30-300 mg/g, macroalbuminuria >300 mg/g — start ACEi/ARB. Lipids: High-intensity statin for all diabetics 40-75; moderate-intensity for <40 with risk factors.

Diagram illustrating Type 2 diabetes pathophysiology showing insulin resistance at cellular level
Figure 5 — Type 2 Diabetes Pathophysiology. In T2DM, peripheral tissues (muscle, fat, liver) develop insulin resistance, and pancreatic beta cells cannot compensate with sufficient insulin production. Source: Wikimedia Commons, by BruceBlaus. Licensed under CC BY 3.0.

06 Dyslipidemia Chronic

Dyslipidemia — elevated LDL-C, low HDL-C, or elevated triglycerides — is a primary driver of atherosclerotic cardiovascular disease. LDL-C is the primary therapeutic target. The 2018 AHA/ACC cholesterol guidelines shifted management from treating to a numeric LDL target toward a risk-based statin intensity approach, though LDL thresholds still guide escalation.

Statin Intensity

IntensityExpected LDL ReductionAgents
High≥50%Atorvastatin 40-80 mg; rosuvastatin 20-40 mg
Moderate30-49%Atorvastatin 10-20 mg; rosuvastatin 5-10 mg; simvastatin 20-40 mg; pravastatin 40-80 mg
Low<30%Simvastatin 10 mg; pravastatin 10-20 mg; lovastatin 20 mg

Who Gets a Statin?

Four statin benefit groups: (1) Clinical ASCVD (MI, stroke, PAD) → high-intensity. (2) LDL ≥190 mg/dL (familial hypercholesterolemia) → high-intensity. (3) Diabetes age 40-75 → moderate-intensity; high-intensity if multiple risk factors or 10-yr ASCVD ≥20%. (4) 10-yr ASCVD risk ≥7.5% age 40-75 → moderate-to-high intensity. For ASCVD patients not at LDL goal (<70 mg/dL), add ezetimibe (Zetia) 10 mg, then PCSK9 inhibitor (evolocumab/Repatha 140 mg q2wk or alirocumab/Praluent 75-150 mg q2wk) if still above target.

Hypertriglyceridemia

Triglycerides ≥500 mg/dL carry risk of acute pancreatitis — treat with fibrate (fenofibrate/Tricor 145 mg daily), omega-3 fatty acids (icosapent ethyl/Vascepa 2g BID — the REDUCE-IT trial showed 25% CV risk reduction), or niacin. For moderate hypertriglyceridemia (150-499), optimize lifestyle (weight loss, reduce refined carbs/alcohol, exercise) and treat underlying causes (uncontrolled DM, hypothyroidism, medications like thiazides, beta-blockers, estrogens, retinoids).

Statins are the most prescribed drug class in the US. Myalgias occur in 5-10% of patients but true rhabdomyolysis is exceedingly rare (~1 in 100,000 patient-years). If a patient develops myalgias: check CK, hold statin, rechallenge with a different statin at a lower dose, or try every-other-day rosuvastatin. Statin-associated muscle symptoms (SAMS) are often nocebo effect — the SAMSON trial showed patients attributed the same symptoms to statin and placebo at similar rates.

07 Obesity & Metabolic Syndrome Chronic

Obesity (BMI ≥30) affects 42% of US adults and is the strongest modifiable risk factor for T2DM, OSA, NAFLD, OA, and multiple cancers (endometrial, breast, colon). Metabolic syndrome — a cluster of insulin resistance-driven findings — is present in ~35% of adults.

Metabolic Syndrome Criteria (ATP III / IDF Harmonized)

Three of five required: (1) Waist circumference ≥102 cm (40 in) in men or ≥88 cm (35 in) in women. (2) Triglycerides ≥150 mg/dL or on treatment. (3) HDL <40 mg/dL in men or <50 mg/dL in women. (4) BP ≥130/85 or on treatment. (5) Fasting glucose ≥100 mg/dL or on treatment. Metabolic syndrome doubles the risk of CVD and quintuples the risk of T2DM.

Anti-Obesity Medications

Agent (Generic/Brand)MechanismExpected Weight LossKey Considerations
Semaglutide 2.4 mg/wk (Wegovy)GLP-1 RA → appetite suppression, delayed gastric emptying~15% total body weight (STEP trials)Nausea, vomiting at initiation; titrate over 16 weeks; pancreatitis risk; CI in MTC/MEN2
Tirzepatide 5-15 mg/wk (Zepbound)Dual GIP/GLP-1 RA~20% total body weight (SURMOUNT trials)Currently highest efficacy; similar GI side effects; titrate over 20 weeks
Phentermine-topiramate ER (Qsymia)Sympathomimetic + anticonvulsant → appetite suppression~10%Contraindicated in pregnancy (topiramate is teratogenic), uncontrolled HTN, hyperthyroidism, glaucoma
Naltrexone-bupropion (Contrave)Opioid antagonist + dopamine/NE reuptake inhibitor → hypothalamic appetite regulation~5-6%Useful if concurrent depression or tobacco use; CI with opioid use, seizure history
Orlistat (Xenical/Alli OTC)Pancreatic lipase inhibitor → ↓ fat absorption by 30%~3-5%GI side effects (steatorrhea, fecal urgency); supplement fat-soluble vitamins (A, D, E, K)

Bariatric surgery: Indicated for BMI ≥40, or BMI ≥35 with obesity-related comorbidities (DM2, OSA, HTN). Options: Roux-en-Y gastric bypass (RYGB, 25-30% weight loss, best DM2 remission), sleeve gastrectomy (most common, 20-25% weight loss), adjustable gastric banding (declining due to complications). Long-term nutritional monitoring required: B12, iron, calcium, vitamin D, folate.

08 Chronic Pain Management Chronic

Chronic pain (lasting >3 months) affects ~50 million US adults. Family physicians prescribe the majority of chronic pain medications and must balance adequate analgesia with opioid risk. The CDC Clinical Practice Guideline for Prescribing Opioids (2022) updated the 2016 guideline with more flexible language but maintained the principle: non-opioid therapy is preferred for chronic non-cancer pain.

WHO Analgesic Ladder (Adapted for Primary Care)

StepAgentIndicationPearl
1 — Non-opioidAcetaminophen (Tylenol) 500-1000 mg q6-8h (max 3g/day); NSAIDs: ibuprofen 400-800 mg q6-8h, naproxen 250-500 mg q12h, meloxicam 7.5-15 mg dailyMild-moderate pain; OA, headache, musculoskeletalNSAIDs: GI bleed risk (add PPI if >65, on ASA, or hx of GI bleed); renal toxicity with chronic use; CV risk with long-term use. Acetaminophen: hepatotoxicity >3g/day
2 — AdjuvantDuloxetine (Cymbalta) 30-60 mg/day; gabapentin 300-3600 mg/day; pregabalin (Lyrica) 75-300 mg BID; TCAs: amitriptyline 10-75 mg qhs, nortriptyline 10-75 mg qhsNeuropathic pain, fibromyalgia, chronic musculoskeletal painDuloxetine is FDA-approved for DPN, fibromyalgia, chronic musculoskeletal pain, and depression — treats pain + mood. Gabapentin: sedation, dizziness; taper to discontinue
3 — Weak opioidTramadol (Ultram) 50-100 mg q4-6h (max 400 mg/day)Moderate pain refractory to steps 1-2Seizure risk (especially with SSRIs/SNRIs — serotonin syndrome); lowers seizure threshold; still carries opioid risks (dependence, respiratory depression)
4 — Strong opioidOxycodone, hydrocodone, morphine — lowest effective dose for shortest durationSevere pain or pain refractory to non-opioid approaches after shared decision-makingCheck PDMP before every prescription; urine drug screen at baseline and periodically; naloxone co-prescribing if ≥50 MME/day or concurrent benzodiazepines
Opioid Risk Mitigation

For patients on chronic opioid therapy: (1) Written treatment agreement/informed consent. (2) Check state PDMP at each refill. (3) Urine drug screen at baseline, then at least annually. (4) Calculate morphine milligram equivalents (MME): ≥50 MME/day = increased overdose risk; ≥90 MME/day = avoid or justify carefully. (5) Co-prescribe naloxone (Narcan) 4 mg nasal spray if ≥50 MME, concurrent benzodiazepines, hx of overdose, or substance use disorder. (6) Avoid concurrent benzodiazepines — combination increases overdose death risk 10-fold. (7) Reassess function, not just pain score — is the patient doing more, not just hurting less?

09 Upper Respiratory Infections & Sinusitis Acute

URIs are the most common reason for ambulatory visits in the US (~500 million/year). The vast majority are viral (rhinovirus, coronavirus, RSV, influenza, parainfluenza, adenovirus). Inappropriate antibiotic prescribing for viral URIs is the single largest driver of antibiotic resistance in the community. Only 0.5-2% of URIs are complicated by bacterial sinusitis.

Acute Bacterial Rhinosinusitis — Diagnostic Criteria

Antibiotics are appropriate ONLY when clinical criteria suggest bacterial infection. Three patterns qualify: (1) Persistent symptoms ≥10 days without improvement (nasal discharge, facial pain/pressure, cough). (2) Severe onset: high fever (≥39°C/102°F) + purulent nasal discharge for ≥3 consecutive days. (3) Double-worsening: symptoms initially improve then worsen again (new fever, increased discharge, headache) around day 5-6. Imaging is NOT recommended for uncomplicated acute sinusitis — clinical diagnosis only.

Treatment

Viral URI: Supportive only — analgesics (acetaminophen, ibuprofen), nasal saline irrigation, honey for cough (age >1 year), dextromethorphan (minimal evidence but commonly used), pseudoephedrine or oxymetazoline nasal spray ≤3 days (rhinitis medicamentosa risk with prolonged use). Antibiotics provide zero benefit and should NOT be prescribed.

Acute bacterial sinusitis (first-line): Amoxicillin-clavulanate (Augmentin) 875/125 mg BID × 5-7 days (standard) or 2000/125 mg BID if risk factors for resistance (recent antibiotics, daycare, region with >10% PRP). Alternatives for penicillin allergy: doxycycline 100 mg BID × 5-7 days, or respiratory fluoroquinolone (levofloxacin 500 mg daily — reserve for true beta-lactam allergy). Watchful waiting for 7 days with analgesics is a valid option for mild bacterial sinusitis per IDSA guidelines.

Most "penicillin allergies" are not true IgE-mediated reactions. Cross-reactivity between penicillin and cephalosporins is <2% (not the historically quoted 10%). If the patient describes a childhood rash, GI upset, or vague reaction, amoxicillin is almost certainly safe. True anaphylaxis to penicillin is the only absolute contraindication to all beta-lactams.

10 Otitis & Pharyngitis Acute

Acute Otitis Media (AOM)

Most common bacterial infection in children. Diagnosis requires: (1) acute onset of symptoms (ear pain, irritability, fever), (2) middle ear effusion (bulging TM, limited mobility on pneumatic otoscopy, air-fluid level), AND (3) signs of middle ear inflammation (erythema of TM, otalgia). A red TM alone is NOT diagnostic — crying makes the TM red.

ScenarioManagement
Age ≥2, unilateral, non-severeObservation option: analgesics × 48-72 hr; prescribe antibiotics if no improvement (safety-net prescription)
Age ≥2, bilateral or severe (fever ≥39°C, severe otalgia, >48 hr symptoms)Amoxicillin 80-90 mg/kg/day divided BID × 10 days (age <2) or 5-7 days (age ≥2)
Age 6-23 months, unilateral, non-severeMay observe with close follow-up OR treat
Age <6 monthsAlways treat: amoxicillin 80-90 mg/kg/day
Treatment failure at 48-72 hrAmoxicillin-clavulanate 90/6.4 mg/kg/day; or ceftriaxone 50 mg/kg IM × 3 days

Pharyngitis — Centor / McIsaac Criteria

CriterionPoints
Tonsillar exudate or swelling+1
Tender anterior cervical lymphadenopathy+1
Fever (subjective or ≥38°C)+1
Absence of cough+1
Age 3-14+1
Age 15-440
Age ≥45−1

Score 0-1: No testing needed, symptomatic care. Score 2-3: Rapid antigen detection test (RADT); treat if positive. Score 4-5: RADT or empiric treatment. For children/adolescents, a negative RADT should be confirmed with throat culture (RADT sensitivity ~85-90%, culture is gold standard). Treatment: penicillin V 500 mg BID × 10 days or amoxicillin 500 mg BID × 10 days; single-dose IM benzathine penicillin G 1.2 million units if adherence is a concern. Goal: prevent acute rheumatic fever (requires treatment within 9 days of symptom onset).

Otoscopic view of a red bulging tympanic membrane consistent with acute otitis media
Figure 6 — Acute Otitis Media. Otoscopic view showing a red, bulging tympanic membrane with effusion — the classic appearance of AOM. Compare with the pearly-gray, translucent normal TM. Source: Wikimedia Commons, by B. Welleschik. Licensed under CC BY-SA 3.0.

11 Urinary Tract Infections Acute

UTIs are the second most common infection seen in primary care. Uncomplicated cystitis occurs almost exclusively in premenopausal, non-pregnant women. Complicated UTI includes: male patients, pregnant patients, catheterized patients, anatomic abnormalities, immunosuppression, and concurrent pyelonephritis.

Uncomplicated Cystitis — Treatment

AgentDoseDurationNotes
Nitrofurantoin (Macrobid)100 mg BID5 daysFirst-line; avoid if eGFR <30; covers E. coli but NOT Proteus or Pseudomonas
TMP-SMX (Bactrim DS)160/800 mg BID3 daysFirst-line if local resistance <20%; avoid in third trimester (kernicterus risk); check sulfa allergy
Fosfomycin (Monurol)3 g single dose1 doseConvenient but slightly less effective; useful for ESBL-producing organisms
Fluoroquinolone (ciprofloxacin, levofloxacin)250-500 mg BID / 250-500 mg daily3 daysReserve for complicated UTI or pyelonephritis; FDA black box: tendon rupture, aortic dissection, neuropathy

Pyelonephritis: Presents with fever, flank pain, CVA tenderness ± nausea/vomiting. Labs: UA with pyuria/bacteriuria, CBC (leukocytosis), blood cultures if febrile. Outpatient treatment (mild): ciprofloxacin 500 mg BID × 7 days or TMP-SMX DS BID × 14 days + single dose ceftriaxone 1g IM. Inpatient criteria: sepsis, vomiting preventing oral intake, pregnancy, obstruction suspected.

Asymptomatic bacteriuria should NOT be treated in non-pregnant adults — it does not reduce UTI frequency and promotes resistance. The only two populations in which screening/treatment of asymptomatic bacteriuria is indicated: (1) pregnant women (screen at 12-16 weeks; untreated increases pyelonephritis risk 20-30-fold) and (2) prior to urologic procedures that breach the mucosal barrier.

12 Skin & Soft Tissue Infections Acute

Skin and soft tissue infections (SSTIs) range from simple cellulitis to necrotizing fasciitis. The primary clinical decision: purulent (abscess likely — I&D is the primary treatment) vs non-purulent (cellulitis/erysipelas — antibiotics are the primary treatment).

SSTI Classification & Management

TypePresentationPathogenTreatment
Simple abscessFluctuant, tender, erythematous nodule ± pustuleMRSA (most common community cause), S. aureusI&D is sufficient for most; antibiotics added if: cellulitis >5 cm surrounding, immunocompromised, multiple abscesses, indwelling device. TMP-SMX DS BID or doxycycline 100 mg BID × 7-10 days
Non-purulent cellulitisSpreading erythema, warmth, tenderness, no drainable collectionGroup A Strep (most common), MSSACephalexin 500 mg QID or dicloxacillin 500 mg QID × 5-7 days. If MRSA concern: add TMP-SMX or doxycycline
ErysipelasSharply demarcated, raised, bright red plaque; face or lower extremityGroup A StrepPenicillin VK 500 mg QID × 5 days; amoxicillin 500 mg TID alternative
Necrotizing fasciitisEMERGENCY — pain out of proportion to exam, rapid spread, crepitus, dusky/necrotic skin, sepsis, bullaeType I (polymicrobial), Type II (GAS), Type III (Vibrio — saltwater/raw seafood)Emergent surgical debridement + broad-spectrum IV antibiotics (vancomycin + piperacillin-tazobactam + clindamycin). Mortality 20-40% even with treatment
Red Flags for Necrotizing Fasciitis

Pain out of proportion to exam findings is the earliest and most important sign. Other red flags: rapidly progressing erythema (mark borders with pen — if spreading visibly over hours, suspect NF), bullae or skin necrosis, crepitus on palpation (gas in tissue), systemic toxicity (fever, tachycardia, hypotension), WBC >15,000 or Na <135. The LRINEC score (Lab Risk Indicator for Necrotizing Fasciitis) uses CRP, WBC, hemoglobin, sodium, creatinine, and glucose to risk-stratify — score ≥6 raises suspicion, ≥8 is strongly suggestive. CT showing gas in soft tissue is diagnostic but do NOT delay surgical consultation waiting for imaging.

13 Acute Low Back Pain Acute

Low back pain is the leading cause of disability worldwide and the second most common reason for primary care visits. ~90% of acute low back pain is nonspecific mechanical pain — no identifiable structural pathology, self-limited within 4-6 weeks. The critical task in primary care is identifying the 1-5% of patients with serious underlying pathology requiring urgent evaluation.

Red Flags — When to Image or Urgently Refer

Red FlagConcernAction
Saddle anesthesia, urinary retention/incontinence, fecal incontinence, bilateral leg weaknessCauda equina syndromeEMERGENT MRI + surgical consult within hours
History of cancer + new back pain, unexplained weight loss, age >50 with new LBPSpinal metastasisMRI with contrast
Fever + back pain, IV drug use, recent spinal procedure, immunosuppressionSpinal epidural abscess / osteomyelitisMRI with contrast + ESR/CRP + blood cultures
Significant trauma (fall, MVC) or minor trauma in osteoporotic patientCompression fractureX-ray first; MRI if neurologic symptoms
Progressive neurologic deficit (foot drop, ascending weakness)Compressive myelopathy or severe radiculopathyUrgent MRI

Management of nonspecific acute LBP: Reassurance (expected to improve in 2-4 weeks), stay active (bed rest worsens outcomes), NSAIDs first-line (ibuprofen 400-600 mg TID or naproxen 500 mg BID), topical heat. Second-line: skeletal muscle relaxant for spasm (cyclobenzaprine 5-10 mg TID × 7-10 days — sedation is common and can be used therapeutically at bedtime). Avoid imaging in the first 6 weeks unless red flags are present — early MRI increases surgery rates without improving outcomes. Avoid opioids as first-line.

14 Acute Abdomen Triage Acute

The family physician's role in acute abdominal pain is pattern recognition and triage — determining who needs emergent surgical evaluation, who needs urgent workup, and who can be managed conservatively. Location of pain is the most useful initial discriminator.

Abdominal Pain by Location — Differential Diagnosis

LocationCommon CausesKey Tests
RUQCholecystitis (Murphy's sign), hepatitis, liver abscess, right-sided pneumonia, Fitz-Hugh-Curtis (PID-associated perihepatitis)RUQ ultrasound, LFTs, lipase
EpigastricPeptic ulcer disease, gastritis, pancreatitis, GERD, MI (inferior wall), aortic dissectionLipase, ECG, CXR if free air suspected
LUQSplenic infarct/rupture, pancreatitis (tail), left lower lobe pneumoniaCT abdomen, CBC
RLQAppendicitis (McBurney's point), ovarian torsion/cyst, ectopic pregnancy, Meckel's diverticulum, mesenteric adenitis (children)CT abdomen/pelvis (adults), US (pediatric/pregnant), beta-hCG in reproductive-age women
LLQDiverticulitis, ovarian pathology, sigmoid volvulus, IBD flareCT abdomen/pelvis
SuprapubicUTI/cystitis, urinary retention, PID, ectopic pregnancyUA, beta-hCG, pelvic ultrasound
DiffuseSBO, mesenteric ischemia, DKA, peritonitis, gastroenteritis, IBDCT with IV contrast, lactate, CBC, BMP
Emergent Surgical Abdomen — Do Not Delay

Involuntary guarding + rigidity = peritonitis until proven otherwise. Upright CXR or CT showing free intraperitoneal air = perforated viscus → emergent surgery. Pain out of proportion to exam with metabolic acidosis and lactate elevation → mesenteric ischemia until proven otherwise (mortality >50% if delayed). Testicular pain in males <25 with high-riding testis and absent cremasteric reflex = testicular torsion → 6-hour window for detorsion. All reproductive-age women with acute abdominal/pelvic pain need a beta-hCG — ruptured ectopic pregnancy kills.

15 Osteoarthritis MSK

Osteoarthritis (OA) is the most common joint disease — affecting >32 million US adults. It is a disease of the entire joint, not just "worn cartilage": cartilage degradation, subchondral bone remodeling, osteophyte formation, synovial inflammation, and ligament/meniscal degeneration all contribute. Most commonly affected joints: knees, hips, hands (DIP > PIP; spares MCPs — this pattern differentiates OA from RA), and spine (facet joints, disc degeneration).

Diagnosis

Clinical diagnosis — imaging is confirmatory, not required. Classic features: joint pain that worsens with activity and improves with rest, morning stiffness <30 minutes (vs RA: >60 minutes), crepitus, bony enlargement (Heberden's nodes = DIP, Bouchard's nodes = PIP), reduced ROM. X-ray findings: Joint space narrowing, osteophytes, subchondral sclerosis, subchondral cysts. Kellgren-Lawrence grading (0-4) quantifies radiographic severity.

Kellgren-Lawrence Classification

GradeRadiographic FindingsClinical Correlation
0NormalNo radiographic OA
1Doubtful — possible osteophytes, no joint space narrowingSymptoms may or may not be present
2Mild — definite osteophytes, possible joint space narrowingIntermittent pain with activity
3Moderate — moderate osteophytes, definite narrowing, some sclerosisRegular pain, functional limitation
4Severe — large osteophytes, marked narrowing, severe sclerosis, bone deformityConstant pain, significant disability; joint replacement candidate

Management

Non-pharmacologic (first-line for all): Weight loss (every 1 lb lost = 4 lbs of pressure off the knee), low-impact exercise (swimming, cycling, walking), physical therapy for strengthening and ROM, knee bracing/orthotics, assistive devices. Pharmacologic: Topical NSAIDs (diclofenac gel — fewer systemic side effects), oral NSAIDs (shortest duration, lowest dose), topical capsaicin, duloxetine 60 mg daily (FDA-approved for OA pain). Intra-articular: Corticosteroid injection (triamcinolone 40 mg for knee — provides 4-8 weeks of relief; limit to 3-4/year per joint). Hyaluronic acid injections have modest evidence. Surgical: Total joint arthroplasty for refractory KL grade 3-4 with failure of conservative management.

16 Tendinopathies & Overuse Injuries MSK

Tendinopathy (formerly "tendinitis") is the preferred term because histology shows collagen degeneration and failed healing, not acute inflammation. Common sites encountered in family medicine:

ConditionLocationExam FindingFirst-Line Treatment
Lateral epicondylitis ("tennis elbow")Common extensor tendon at lateral epicondylePain with resisted wrist extension and grip; tenderness over lateral epicondyleRelative rest, counterforce brace, eccentric wrist extension exercises, topical NSAID
Medial epicondylitis ("golfer's elbow")Common flexor tendon at medial epicondylePain with resisted wrist flexion and forearm pronationSame principles as lateral; less common
Rotator cuff tendinopathySupraspinatus (most common), infraspinatusPainful arc (60-120° abduction), positive Neer's and Hawkins impingement tests, weakness with external rotation (infraspinatus)PT (rotator cuff strengthening, scapular stabilization), subacromial corticosteroid injection if refractory
De Quervain's tenosynovitis1st dorsal compartment (APL, EPB tendons)Positive Finkelstein's test (ulnar deviation of wrist with thumb in fist → pain over radial styloid)Thumb spica splint, corticosteroid injection into 1st dorsal compartment (cure rate ~80%)
Plantar fasciitisPlantar fascia at calcaneal insertionFirst-step morning pain, tenderness at medial calcaneal tubercleCalf/plantar stretching, supportive footwear, night splint, NSAIDs; corticosteroid injection if >6 weeks refractory (risk of fat pad atrophy)
Achilles tendinopathyAchilles tendon (mid-substance or insertional)Pain with palpation 2-6 cm above calcaneus (mid-substance); pain at insertion (insertional); positive Thompson test rules out ruptureEccentric heel drop exercises (Alfredson protocol), heel lifts, avoid fluoroquinolones (tendon rupture risk)
Corticosteroid injections for tendinopathy provide short-term relief (4-6 weeks) but may impair long-term tendon healing. Increasingly, eccentric loading exercises are considered the definitive treatment for most tendinopathies. PRP injections show promise but evidence remains mixed and they are not uniformly covered by insurance.

17 Chronic Low Back Pain MSK

Chronic LBP persists beyond 12 weeks. Unlike acute LBP, chronic LBP is a biopsychosocial condition: psychosocial factors (depression, catastrophizing, job dissatisfaction, fear-avoidance behavior) are stronger predictors of chronicity than MRI findings. Up to 60% of asymptomatic adults have disc bulges on MRI — imaging findings often do not correlate with symptoms.

Management Hierarchy

First-line: Exercise therapy (core stabilization, yoga, tai chi — all have Level A evidence), cognitive behavioral therapy (CBT), interdisciplinary rehabilitation. Second-line: Duloxetine 60 mg daily (FDA-approved for chronic musculoskeletal pain), NSAIDs for flares, spinal manipulation (modest short-term benefit). Third-line: Gabapentin/pregabalin if radicular component; tramadol only if non-opioid approaches have failed. Avoid: Chronic opioids (no evidence of long-term benefit for CLBP and substantial harm), passive modalities (ultrasound, TENS — minimal evidence), repeat imaging without new red flags, surgery for nonspecific LBP.

When to refer for surgery: Cauda equina syndrome (emergent). Progressive motor deficit (urgent). Radiculopathy with concordant MRI findings refractory to 6-8 weeks of conservative care. Spinal stenosis with neurogenic claudication limiting function despite physical therapy.

18 Osteoporosis MSK

Osteoporosis is a systemic skeletal disease characterized by low bone mass and microarchitectural deterioration → increased fracture risk. Affects 10 million Americans (80% women). Hip fractures carry 20-30% one-year mortality in elderly patients. The USPSTF recommends DEXA screening for all women ≥65 and postmenopausal women <65 with risk factors (FRAX tool).

T-Score Classification (WHO)

T-ScoreClassificationClinical Action
≥ −1.0NormalRescreen based on risk factors
−1.0 to −2.5OsteopeniaFRAX assessment; treat if 10-yr hip fracture risk ≥3% or major osteoporotic fracture ≥20%
≤ −2.5OsteoporosisPharmacotherapy + calcium/vitamin D + fall prevention
≤ −2.5 with fragility fractureSevere osteoporosisAggressive treatment; consider anabolic agent first

Pharmacotherapy

AgentMechanismDosingPearl
Alendronate (Fosamax)Bisphosphonate — inhibits osteoclast resorption70 mg PO weeklyTake on empty stomach with full glass of water, remain upright 30 min (esophageal erosion risk); drug holiday after 5 yr PO or 3 yr IV
Risedronate (Actonel)Bisphosphonate35 mg PO weekly or 150 mg monthlySame precautions as alendronate
Zoledronic acid (Reclast)IV bisphosphonate5 mg IV annuallyBest adherence; flu-like reaction common after first infusion; check vitamin D and renal function before
Denosumab (Prolia)RANKL inhibitor → decreases osteoclast formation60 mg SubQ q6monthsNo renal dose adjustment; rebound vertebral fractures if discontinued — must transition to bisphosphonate
Teriparatide (Forteo)PTH analog — anabolic (stimulates osteoblasts)20 mcg SubQ daily × 2 yearsFor severe osteoporosis or fracture despite bisphosphonate; must follow with antiresorptive agent; black box: osteosarcoma in rats
Romosozumab (Evenity)Sclerostin inhibitor — anabolic + antiresorptive210 mg SubQ monthly × 12 monthsMost potent for BMD gain; black box: CV risk (avoid within 1 yr of MI/stroke); follow with bisphosphonate or denosumab

Supplementation baseline: Calcium 1000-1200 mg/day (dietary + supplement if needed), vitamin D 800-1000 IU/day (target 25-OH vitamin D ≥30 ng/mL). Weight-bearing exercise and fall prevention are essential non-pharmacologic components.

19 Depression & Anxiety Behavioral

Depression and anxiety are the two most common mental health conditions in primary care. Family physicians manage the majority of depression and anxiety in the US — only ~20% of patients are referred to psychiatry. The PHQ-9 (depression) and GAD-7 (anxiety) are validated screening and monitoring instruments used at nearly every primary care encounter.

PHQ-9 Scoring

ScoreSeverityManagement
0-4MinimalNo treatment; reassess if clinically indicated
5-9MildWatchful waiting, lifestyle modifications, consider therapy (CBT)
10-14ModerateAntidepressant OR psychotherapy; combination preferred if available
15-19Moderately severeAntidepressant + psychotherapy strongly recommended
20-27SevereAntidepressant + psychotherapy; consider psychiatry referral

Antidepressant Selection

Class / AgentDose RangeKey FeatureSide Effects / Pearl
SSRI — sertraline (Zoloft)50-200 mg/dayFirst-line for MDD and most anxiety disorders; safe in cardiac patientsGI side effects (nausea, diarrhea); sexual dysfunction 30-50%; avoid abrupt discontinuation
SSRI — escitalopram (Lexapro)10-20 mg/dayBest tolerated SSRI; fewest drug interactionsQTc prolongation at 20 mg — ECG if >65 or cardiac hx; max 10 mg if >65
SSRI — fluoxetine (Prozac)20-80 mg/dayLong half-life (5 days) — no discontinuation syndrome; preferred in non-adherent patientsMost activating SSRI; CYP2D6 inhibitor (drug interactions)
SNRI — duloxetine (Cymbalta)30-120 mg/dayDepression + chronic pain + fibromyalgia + DPNHepatotoxicity with heavy alcohol use; nausea; BP elevation at higher doses
SNRI — venlafaxine XR (Effexor XR)75-225 mg/dayEffective for treatment-resistant depression; GAD approvedDose-dependent hypertension; worst discontinuation syndrome of all antidepressants; taper very slowly
Bupropion (Wellbutrin XL)150-450 mg/dayNo sexual dysfunction, no weight gain; helps with smoking cessation; activatingContraindicated in seizure disorders, eating disorders; lower seizure threshold; not effective for anxiety
Mirtazapine (Remeron)15-45 mg/daySedating, appetite-stimulating — good for depressed elderly with insomnia and weight lossWeight gain, sedation (paradoxically more sedating at 15 mg than 45 mg); no sexual dysfunction
All antidepressants carry a black box warning for suicidal ideation in patients <25 — this does NOT mean they should be avoided; it means close follow-up (contact within 1 week, visit at 2-4 weeks). The actual suicide rate decreases with antidepressant treatment. Allow 4-6 weeks at adequate dose before declaring treatment failure. If partial response at 6 weeks: optimize dose, augment (add bupropion to SSRI, or low-dose aripiprazole 2-5 mg), or switch class.

GAD-7 and Anxiety Management

GAD-7 scoring: 0-4 minimal, 5-9 mild, 10-14 moderate, 15-21 severe. First-line pharmacotherapy for generalized anxiety disorder: SSRIs (sertraline, escitalopram) or SNRIs (duloxetine, venlafaxine). Buspirone (BuSpar) 10-30 mg/day in divided doses is a non-addictive anxiolytic — takes 2-4 weeks for full effect. Benzodiazepines (lorazepam, alprazolam) for short-term use ONLY (<2-4 weeks) — high addiction potential, cognitive impairment, fall risk in elderly, rebound anxiety. CBT is equally effective as medication for mild-moderate anxiety and should be offered to all patients.

Chemical structure of serotonin, the primary neurotransmitter targeted by SSRI antidepressants
Figure 7 — Serotonin (5-HT) Structure. Serotonin is the primary neurotransmitter modulated by SSRIs and SNRIs. SSRIs block the serotonin transporter (SERT) in the synaptic cleft, increasing serotonin availability. Source: Wikimedia Commons. Public domain.

20 ADHD Behavioral

Attention-deficit/hyperactivity disorder (ADHD) affects 5-7% of children and 2.5-4% of adults. Family physicians diagnose and manage the majority of pediatric ADHD. DSM-5 requires 6+ symptoms of inattention and/or hyperactivity-impulsivity persisting ≥6 months, present before age 12, in ≥2 settings (home + school/work), with functional impairment.

Pharmacotherapy

Agent (Generic/Brand)ClassDosingDurationPearl
Methylphenidate IR (Ritalin)Stimulant (dopamine/NE reuptake inhibitor)5-60 mg/day divided BID-TID3-4 hoursStart low, titrate weekly; first-line in children ≥6
Methylphenidate ER (Concerta)Stimulant18-72 mg daily10-12 hoursOROS delivery; cannot crush; avoids noon dose at school
Amphetamine mixed salts (Adderall XR)Stimulant (dopamine/NE release + reuptake inhibition)5-30 mg daily10-12 hoursMay be more effective if methylphenidate fails; higher abuse potential
Lisdexamfetamine (Vyvanse)Prodrug stimulant20-70 mg daily12-14 hoursRequires enzymatic conversion — lower abuse potential; also FDA-approved for binge eating disorder
Atomoxetine (Strattera)Non-stimulant (NE reuptake inhibitor)40-100 mg daily (adults)24 hoursNo abuse potential; takes 4-6 weeks for full effect; useful if tics, anxiety, or substance use concerns
Guanfacine ER (Intuniv)Non-stimulant (alpha-2 agonist)1-4 mg daily24 hoursSedation, hypotension; helpful for hyperactivity/impulsivity predominant; can augment stimulants

AAP guidelines for children: Age 4-5: behavioral therapy first, methylphenidate if inadequate response. Age 6-11: stimulant medication + behavioral therapy (combined is superior). Age ≥12: stimulant medication with or without behavioral therapy. Monitor: height, weight (growth charts — stimulants can suppress appetite/growth), heart rate, blood pressure, tics, sleep, mood.

21 Substance Use Disorders Behavioral

Substance use disorders (SUDs) are among the most under-recognized and undertreated conditions in primary care. Family physicians are uniquely positioned to screen (SBIRT: Screening, Brief Intervention, Referral to Treatment), initiate medication-assisted treatment (MAT), and provide longitudinal care. Alcohol use disorder (AUD) and opioid use disorder (OUD) are the two SUDs most commonly managed in the primary care setting.

Alcohol Use Disorder

Screening: AUDIT-C (3 questions, score ≥4 men / ≥3 women = positive screen) or CAGE (2+ positive = concerning). DSM-5 AUD: ≥2 of 11 criteria in a 12-month period (mild: 2-3; moderate: 4-5; severe: 6+).

Pharmacotherapy for AUD:

AgentMechanismDosePearl
Naltrexone (ReVia, Vivitrol)Opioid antagonist → reduces reward from drinking50 mg PO daily or 380 mg IM monthlyMost effective for reducing heavy drinking days; contraindicated if on opioids; check LFTs
Acamprosate (Campral)Glutamate modulator → reduces craving in abstinence666 mg TIDWorks best after detox in abstinent patients; dose-adjust for renal impairment; no hepatotoxicity (advantage over naltrexone)
Disulfiram (Antabuse)Aldehyde dehydrogenase inhibitor → aversive reaction with alcohol250-500 mg dailyCauses nausea, vomiting, flushing, headache if alcohol consumed; requires high motivation; hepatotoxicity risk

Opioid Use Disorder

Buprenorphine-naloxone (Suboxone): Partial mu-opioid agonist. Family physicians can prescribe buprenorphine — the X-waiver requirement was eliminated in 2023. Induction: patient must be in moderate withdrawal (COWS score ≥8-12); start 2-4 mg SL, may repeat in 1-2 hours, typical day-1 dose 8-16 mg. Maintenance: 16-24 mg/day. Has a ceiling effect for respiratory depression — much safer than methadone. Common induction pitfall: starting too early precipitates withdrawal (buprenorphine displaces full agonists from receptors).

Naltrexone (Vivitrol) 380 mg IM monthly: Full opioid antagonist. Patient must be opioid-free for 7-10 days before starting (precipitated withdrawal risk). Best for highly motivated patients or those in controlled environments (drug court, sober living).

22 Insomnia Behavioral

Chronic insomnia (difficulty initiating or maintaining sleep ≥3 nights/week for ≥3 months) affects 10-15% of adults. First-line treatment is NOT medication — it is cognitive behavioral therapy for insomnia (CBT-I), which has better long-term efficacy than any pharmacotherapy and no side effects.

CBT-I Components

Sleep restriction: Limit time in bed to actual sleep time (e.g., if sleeping 5 hr but in bed 8 hr, restrict to 5 hr; gradually increase by 15-30 min as efficiency improves; target sleep efficiency ≥85%). Stimulus control: Bed is for sleep and sex only; leave bed if awake >20 minutes. Sleep hygiene: Consistent wake time, dark/cool room, no screens 1 hr before bed, limit caffeine after noon, avoid alcohol. Cognitive restructuring: Address catastrophic beliefs about sleep consequences.

Pharmacotherapy (Second-Line)

AgentMechanismDosePearl
MelatoninMT1/MT2 receptor agonist0.5-5 mg 1-2 hr before bedMost evidence for circadian rhythm disorders and jet lag; minimal evidence for chronic insomnia; OTC; low risk
Trazodone5-HT2A antagonist + weak SERT inhibitor25-100 mg qhsMost commonly prescribed off-label sleep aid; not FDA-approved for insomnia; priapism (rare); minimal dependence
Suvorexant (Belsomra)Dual orexin receptor antagonist (DORA)10-20 mg qhsFDA-approved; no rebound insomnia; avoid with strong CYP3A4 inhibitors; expensive
Lemborexant (DayVigo)DORA5-10 mg qhsSimilar to suvorexant; may have slight advantage for sleep maintenance
Zolpidem (Ambien)Non-benzodiazepine GABA-A agonist5 mg (women) / 5-10 mg (men) qhsFDA lowered female dose due to next-morning impairment; sleepwalking, sleep-driving risk; short-term only (<4 weeks)
Doxepin (Silenor)H1 antihistamine at low dose3-6 mg qhsFDA-approved for sleep maintenance insomnia; safe in elderly (minimal anticholinergic at this dose)
Avoid benzodiazepines for chronic insomnia — tolerance develops within 2-4 weeks, dependence is common, and fall/fracture risk in elderly is significantly increased. Diphenhydramine (Benadryl) and hydroxyzine are on the Beers Criteria list for inappropriate use in elderly due to anticholinergic effects (confusion, urinary retention, constipation, dry mouth, tachycardia). Z-drugs (zolpidem, zaleplon, eszopiclone) carry similar risks of dependence and parasomnias.

23 Contraception Women's Health

Family physicians provide the majority of contraceptive care in the US. Contraceptive counseling should be patient-centered, using the tiered-effectiveness model (LARC → hormonal → barrier) while respecting patient autonomy.

Contraceptive Methods by Effectiveness

MethodTypical-Use Failure RateMechanismDurationKey Consideration
Copper IUD (Paragard)0.8%Spermicidal Cu2+ ions; inflammatory reaction prevents implantation10-12 yearsNon-hormonal; heavier periods; can serve as emergency contraception (within 5 days)
LNG-IUD (Mirena, Kyleena, Liletta)0.1-0.4%Local progestin → thins endometrium, thickens cervical mucus3-8 years (device-dependent)Reduces menstrual bleeding (treats menorrhagia); Mirena FDA-approved for heavy periods
Etonogestrel implant (Nexplanon)0.1%Progestin → suppresses ovulation, thickens mucus3-5 yearsMost effective reversible contraceptive; irregular bleeding most common reason for discontinuation
DMPA injection (Depo-Provera)4%Progestin → suppresses ovulationEvery 3 monthsWeight gain, bone density loss (reversible); delayed return to fertility (up to 10 months)
Combined OCP (various)7%Estrogen + progestin → suppress ovulation, thin endometrium, thicken mucusDaily pillContraindicated in smokers ≥35, migraine with aura, VTE history, breast cancer (use CDC MEC categories)
Progestin-only pill (Norethindrone 0.35 mg)7%Thickens mucus; inconsistently suppresses ovulationDaily pill (3-hour window)Safe for breastfeeding, smokers ≥35, migraine with aura; new POP: norgestrel (Opill) available OTC 2024
Patch (Xulane) / Ring (NuvaRing)7%Combined hormonal — transdermal/vaginal absorptionWeekly patch / monthly ringSame contraindications as OCP; patch less effective in women >90 kg
Male condom13%BarrierPer useOnly method that prevents STIs (dual method recommended with hormonal)

CDC Medical Eligibility Criteria (MEC) — Key Category 4 Contraindications

Category 4 = unacceptable health risk: Combined hormonal contraceptives (CHC) are Category 4 with: current or hx of VTE/PE, ischemic heart disease, stroke, migraine with aura, breast cancer, smoker ≥35 (if ≥15 cigarettes/day), <3 weeks postpartum, hepatocellular adenoma, severe cirrhosis, SLE with antiphospholipid antibodies. The progestin-only methods (IUD, implant, DMPA, POP) have very few Category 4 contraindications and are safe in nearly all patients.

Diagram of an intrauterine device placed inside the uterus for long-acting reversible contraception
Figure 8 — Intrauterine Device (IUD). The IUD sits within the uterine cavity and provides long-acting reversible contraception. The copper IUD releases Cu2+ ions; the hormonal IUD releases levonorgestrel locally. Source: Wikimedia Commons, by BruceBlaus. Licensed under CC BY 3.0.

24 Prenatal Care Women's Health

Family physicians deliver ~20% of babies in the US and provide the majority of prenatal care in rural settings. Standard prenatal visit schedule: monthly through 28 weeks, biweekly 28-36 weeks, weekly 36 weeks to delivery. First visit ideally at 8-10 weeks.

Prenatal Visit Laboratory Schedule

TimingLabs & Tests
Initial visit (8-10 wk)CBC, blood type/Rh/antibody screen, rubella immunity, hepatitis B surface antigen, HIV, RPR/VDRL, UA + culture, Pap if due, chlamydia/gonorrhea (NAAT), urine hCG confirmation
11-14 weeksFirst trimester screen (NT ultrasound + PAPP-A + free beta-hCG) or cell-free DNA (NIPT) for aneuploidy
15-20 weeksQuad screen (if no first-trimester screen), AFP for neural tube defects, anatomy ultrasound at 18-22 weeks
24-28 weeks1-hr glucose challenge test (50g GCT; ≥140 → 3-hr 100g OGTT for GDM), CBC (screen for anemia), Rh antibody screen (if Rh-negative: give RhoGAM 300 mcg IM at 28 wk)
35-37 weeksGroup B Strep (GBS) vaginal-rectal culture; if positive, intrapartum penicillin G prophylaxis
36+ weeksConfirm fetal presentation (Leopold's maneuvers/ultrasound); discuss labor plan; screen for preeclampsia (BP, proteinuria)

Common Prenatal Complications

Gestational diabetes (GDM): Diagnosed when 2+ of 4 values on 3-hr OGTT are abnormal (fasting ≥95, 1-hr ≥180, 2-hr ≥155, 3-hr ≥140 mg/dL). Management: dietary modification + glucose monitoring (fasting <95, 1-hr postprandial <140, 2-hr <120); insulin is first-line pharmacotherapy if diet fails (metformin and glyburide used but NOT FDA-approved for pregnancy).

Preeclampsia: New-onset hypertension (≥140/90 on 2 occasions ≥4 hours apart) after 20 weeks with proteinuria (≥300 mg/24hr or protein/creatinine ratio ≥0.3) or end-organ dysfunction (platelets <100K, Cr >1.1, elevated LFTs, pulmonary edema, cerebral/visual symptoms). Severe features: SBP ≥160 or DBP ≥110, thrombocytopenia, renal insufficiency, liver dysfunction, or symptoms. Definitive treatment: delivery. Magnesium sulfate for seizure prophylaxis (eclampsia prevention). Low-dose aspirin (81 mg starting 12-16 weeks) is recommended for high-risk women to prevent preeclampsia.

25 Menopause Women's Health

Menopause is defined as 12 consecutive months of amenorrhea without other cause, reflecting ovarian follicular depletion. Average age: 51 years. Perimenopause (the transition) begins 4-8 years before final menstrual period and is characterized by irregular cycles, vasomotor symptoms, and hormone fluctuations. Diagnosis is clinical — FSH testing is rarely needed (and unreliable during perimenopause due to fluctuations).

Vasomotor Symptoms — Management

Hormone therapy (HT): Most effective treatment for hot flashes and vaginal atrophy. Estrogen alone (for women without a uterus) or combined estrogen + progestogen (for women with a uterus — progestogen prevents endometrial hyperplasia/cancer). Standard: conjugated equine estrogens (CEE/Premarin) 0.3-0.625 mg/day or transdermal estradiol patch 0.025-0.05 mg/day + medroxyprogesterone acetate (MPA) 2.5 mg daily or micronized progesterone 100-200 mg daily. Initiate within 10 years of menopause or age <60 for best risk-benefit ratio (WHI "timing hypothesis"). Contraindicated in: breast cancer, VTE, stroke, MI, active liver disease.

Non-hormonal options: Fezolinetant (Veozah) 45 mg daily — first NK3 receptor antagonist, FDA-approved 2023, reduces hot flashes ~60%. Paroxetine 7.5 mg (Brisdelle) — only FDA-approved SSRI for vasomotor symptoms. Venlafaxine 37.5-75 mg, gabapentin 300-900 mg qhs (off-label but effective). CBT also reduces vasomotor symptom severity.

Genitourinary syndrome of menopause (GSM): Vaginal dryness, dyspareunia, urinary frequency/urgency. First-line: vaginal moisturizers (Replens) + lubricants. If insufficient: low-dose vaginal estrogen (estradiol cream 0.5g 2×/wk, estradiol ring/Estring, estradiol vaginal tablet) — minimal systemic absorption, safe even in many breast cancer survivors (discuss with oncologist). Ospemifene (Osphena) 60 mg PO daily is an oral SERM alternative.

26 Cervical & Breast Cancer Screening Women's Health

Cervical Cancer Screening

Age GroupRecommended ScreeningFrequency
<21No screening (regardless of sexual activity)
21-29Cytology (Pap) aloneEvery 3 years
30-65Pap + hrHPV co-testing (preferred) OR hrHPV alone OR Pap aloneCo-testing q5yr; hrHPV alone q5yr; Pap alone q3yr
>65Stop if adequate prior negative screening (3 consecutive negative Paps or 2 negative co-tests in prior 10 years)
Post-hysterectomy (supracervical → continue; total with cervix removed for benign disease and no CIN2+ history)Stop

Abnormal Pap management (ASCCP 2019): Risk-based approach using current and prior results. LSIL with negative HPV → repeat in 1 year. LSIL or ASC-US with positive HPV → colposcopy. HSIL → expedited treatment (LEEP) or colposcopy with biopsy. CIN1 → surveillance. CIN2/3 → excisional treatment (LEEP/cold knife cone).

Breast Cancer Screening

USPSTF (2024): Biennial mammography for all women aged 40-74. ACS: Annual mammography starting at 45 (may start at 40 with shared decision-making); biennial at 55+. For high-risk women (BRCA carriers, ≥20% lifetime risk by models, chest radiation 10-30): annual mammography + breast MRI starting at 25-30. Clinical breast exam: no longer specifically recommended by USPSTF but still performed in practice.

BI-RADS Classification:

CategoryAssessmentAction
0Incomplete — needs additional imagingCallback for diagnostic mammogram, ultrasound, or MRI
1NegativeRoutine screening
2Benign findingRoutine screening
3Probably benign (<2% malignancy risk)Short-interval follow-up at 6 months
4Suspicious (2-95% malignancy risk)Tissue diagnosis (biopsy)
5Highly suggestive of malignancy (≥95%)Tissue diagnosis (biopsy)
6Known biopsy-proven malignancySurgical management
A mammography image showing the standard craniocaudal view of breast tissue
Figure 9 — Mammography. A standard mammographic view used for breast cancer screening. Mammography remains the gold standard screening modality, reducing breast cancer mortality by 20-30% in screened populations. Source: Wikimedia Commons. Public domain.

27 Well-Child Visits & Milestones Pediatric

The AAP Bright Futures schedule defines well-child visit timing: newborn, 1 month, 2, 4, 6, 9, 12, 15, 18, 24, 30 months, then annually 3-21 years. Each visit includes growth assessment (plotted on CDC growth charts — weight, length/height, head circumference through 24 months, BMI starting at age 2), developmental screening, immunizations, and anticipatory guidance.

Key Developmental Milestones

AgeGross MotorFine MotorLanguageSocial
2 monthsLifts head proneHands open 50%Coos, social smileRecognizes parent
4 monthsRolls front to backReaches, grasps rattleLaughs, squealsEnjoys social play
6 monthsSits with support, rolls both waysTransfers objects hand to handBabbles consonants (ba, da)Stranger anxiety begins
9 monthsPulls to stand, crawlsPincer grasp developingMama/dada (nonspecific)Separation anxiety, object permanence
12 monthsCruises, may walk independentlyMature pincer grasp1-3 words, follows simple commandsPoints to show interest, waves bye
18 monthsWalks well, climbs stairs with hand heldStacks 2-4 blocks, scribbles10-25 words, points to body partsParallel play, imitates
2 yearsRuns, kicks ball, climbsStacks 6 blocks, turns pages2-word phrases ("want milk"), 50+ wordsParallel play, follows 2-step commands
3 yearsPedals tricycle, balances briefly on one footDraws circle, uses scissors3-word sentences, 75% intelligible to strangersInteractive play, takes turns
4 yearsHops on one foot, climbs stairs alternating feetDraws square, dresses selfComplex sentences, tells stories, 100% intelligibleCooperative play, imaginary friends
5 yearsSkips, catches ballDraws triangle, ties shoes (by 6)Counts to 10, knows colors, follows 3-step commandsUnderstands rules, plays organized games
Developmental screening (not just surveillance) with a validated tool is recommended at 9, 18, and 30 months (ASQ-3 or PEDS). Autism-specific screening with M-CHAT-R/F is recommended at 18 and 24 months. A child not meeting milestones should trigger early intervention referral — do not "wait and see." Early intervention (before age 3) significantly improves outcomes for ASD and developmental delay.
Infant being weighed on a clinical scale during a well-child visit
Figure 10 — Well-Child Growth Assessment. Serial weight and length measurements plotted on growth charts are fundamental to pediatric surveillance. A child crossing 2 major percentile lines warrants further evaluation. Source: Wikimedia Commons. Public domain.

28 Immunization Schedule Pediatric

The CDC/ACIP immunization schedule is the most frequently referenced guideline in family medicine. Keeping children on schedule prevents an estimated 42,000 deaths per year in the US. The schedule is updated annually; the core childhood series:

Childhood Immunization Schedule (Birth-6 Years)

VaccineDosesSchedulePearl
Hepatitis B (HepB)3Birth, 1 month, 6 monthsFirst dose within 24 hours of birth; if mother HBsAg+: HBIG + vaccine within 12 hours
Rotavirus (RV)2-32, 4 months (Rotarix/2-dose) or 2, 4, 6 months (RotaTeq/3-dose)Oral live vaccine; do not start after 15 weeks; must complete by 8 months
DTaP (diphtheria, tetanus, acellular pertussis)52, 4, 6, 15-18 months, 4-6 yearsSwitch to Tdap at age 11-12; then Td or Tdap q10 years
Hib (H. influenzae type b)3-42, 4, 6 (PRP-T), 12-15 monthsDramatically reduced epiglottitis and bacterial meningitis
PCV15 or PCV20 (pneumococcal)3-42, 4, 6, 12-15 monthsPCV15 may need PPSV23 follow-up in high-risk children
IPV (inactivated polio)42, 4, 6-18 months, 4-6 yearsNo oral polio (OPV) used in US since 2000
MMR (measles, mumps, rubella)212-15 months, 4-6 yearsLive vaccine; contraindicated in pregnancy and severe immunodeficiency; NO causal link to autism
Varicella212-15 months, 4-6 yearsLive vaccine; avoid in immunocompromised; if ≥13 years and not immune: 2 doses 4-8 weeks apart
Hepatitis A (HepA)212 months, 18 months (6-18 months apart)Universal childhood vaccination since 2006
InfluenzaAnnual≥6 months annuallyFirst-ever flu vaccine in children <9 years: 2 doses 4 weeks apart

29 Common Pediatric Conditions Pediatric

Croup (Laryngotracheobronchitis)

Peak age 6 months - 3 years. Cause: parainfluenza virus (75%). Classic presentation: barky/seal-like cough, inspiratory stridor, hoarse voice, preceded by URI prodrome. Steeple sign on AP neck X-ray (subglottic narrowing — but X-ray rarely needed). Management: mild (no stridor at rest) → single dose dexamethasone 0.6 mg/kg PO/IM (max 10 mg). Moderate-severe (stridor at rest) → dexamethasone + nebulized racemic epinephrine 0.5 mL of 2.25% in 3 mL NS (observe 2-4 hours for rebound). Red flag: drooling + tripod positioning + toxic appearance = think epiglottitis (now rare post-Hib vaccine).

Pediatric Asthma

Most common chronic disease of childhood. Diagnosis in children ≥5: spirometry showing reversible obstruction (FEV1 improvement ≥12% after bronchodilator). In children <5: clinical diagnosis based on recurrent wheezing (≥3 episodes), symptom pattern, and response to therapy.

Severity (age ≥5)SymptomsNighttime AwakeningsFEV1Step Therapy
Intermittent≤2 days/week≤2×/month>80%Step 1: SABA PRN (albuterol)
Mild persistent>2 days/week but not daily3-4×/month≥80%Step 2: Low-dose ICS (fluticasone 44-88 mcg BID) or PRN ICS-formoterol
Moderate persistentDaily>1×/week60-80%Step 3: Low-dose ICS + LABA (fluticasone/salmeterol) or medium-dose ICS
Severe persistentThroughout dayNightly<60%Step 4-5: Medium/high-dose ICS + LABA; consider add-on (LAMA, biologic, oral steroids)

Acute Otitis Media (Pediatric) — see also Section 10

Most common bacterial infection in children. Risk factors: age <2, daycare attendance, second-hand smoke, bottle-propping, pacifier use after 6 months. Pathogens: S. pneumoniae, non-typeable H. influenzae, M. catarrhalis. Prevention: pneumococcal vaccine, influenza vaccine, breastfeeding.

Febrile Seizures

Occur in 2-5% of children ages 6 months to 5 years. Simple febrile seizure: generalized tonic-clonic, <15 minutes, does not recur within 24 hours. Management: parental reassurance, treat underlying fever source; no antiepileptic drugs, no neuroimaging, no EEG needed. Complex febrile seizure: focal, >15 minutes, or recurrent within 24 hours → consider EEG and workup for other causes. Simple febrile seizures do NOT increase epilepsy risk significantly (2% vs 1% baseline).

30 Adolescent Health Pediatric

Adolescent visits (11-21 years) require a unique approach: confidential screening for high-risk behaviors, STI screening, contraception counseling, and mental health assessment. The HEEADSSS psychosocial assessment framework: Home, Education/Employment, Eating, Activities, Drugs, Sexuality, Suicide/depression, Safety.

Adolescent-Specific Screening & Vaccines

ItemAgeDetails
HPV vaccine (Gardasil 9)11-12 (routine); catch-up through 262 doses if started <15 (0, 6-12 months); 3 doses if started ≥15 (0, 1-2, 6 months); prevents cervical, anal, oropharyngeal cancers + genital warts
Tdap booster11-12Single dose replacing Td; then Td or Tdap q10 years
Meningococcal ACWY (MenACWY)11-12, booster at 16Quadrivalent; booster at 16 provides coverage through college
Meningococcal B (MenB)16-23 (shared decision-making)Not routinely recommended; 2-3 dose series
Depression screening≥12 annuallyPHQ-A (adolescent-modified); Columbia Suicide Severity Rating Scale if positive
STI screeningSexually active: chlamydia/gonorrhea annually (women <25, MSM); HIV at least once ≥15NAAT urine or vaginal/cervical swab
Confidentiality is critical in adolescent medicine. In most states, minors can consent independently for STI testing/treatment, contraception, mental health, and substance use treatment. A useful framework: begin the visit with the parent present, then ask the parent to leave for a portion of the visit to screen for sensitive topics. Document what the adolescent permits to be shared with the parent.

31 Polypharmacy & Deprescribing Geriatric

Polypharmacy (typically defined as ≥5 concurrent medications) affects >40% of adults ≥65. It is a direct cause of adverse drug events (ADEs), falls, cognitive impairment, hospitalization, and mortality. The family physician manages the medication list longitudinally and is best positioned to deprescribe — the systematic process of reducing or stopping medications that are no longer beneficial or are potentially harmful.

Beers Criteria — High-Risk Medications in Elderly (Selected)

Drug / ClassRisk in ElderlyAlternative
Benzodiazepines (diazepam, lorazepam, alprazolam)Falls, fractures, cognitive impairment, dependenceCBT-I for insomnia; SSRI/buspirone for anxiety
Anticholinergics (diphenhydramine, hydroxyzine, oxybutynin, TCAs at high dose)Confusion, delirium, dry mouth, urinary retention, constipation, tachycardiaLoratadine/cetirizine for allergies; mirabegron for OAB; trazodone/melatonin for sleep
NSAIDs (chronic use)GI bleed, renal impairment, HTN, HF exacerbationTopical NSAIDs, acetaminophen, duloxetine, non-pharmacologic pain management
Proton pump inhibitors (chronic >8 weeks without indication)C. difficile, pneumonia, hypomagnesemia, osteoporotic fractures, CKDH2 blocker (famotidine), step-down and discontinue if no ongoing indication
Sulfonylureas (glyburide especially)Prolonged hypoglycemia (long half-life, renal clearance)Glipizide (shorter acting), DPP-4i, or relaxed A1C targets
Skeletal muscle relaxants (cyclobenzaprine, methocarbamol)Sedation, anticholinergic effects, fall riskPT, topical agents, non-pharmacologic

Deprescribing Process

Step 1: Reconcile the complete medication list (include OTC, supplements, herbals). Step 2: Identify potentially inappropriate medications (PIMs) using Beers Criteria, STOPP/START criteria, or deprescribing algorithms (deprescribing.org). Step 3: Prioritize — target drugs with highest harm potential and lowest current benefit. Step 4: Taper (do not abruptly stop benzodiazepines, opioids, beta-blockers, corticosteroids, or antidepressants). Step 5: Monitor for withdrawal or return of original condition. Step 6: Repeat at each visit. Deprescribe one medication at a time to attribute any changes.

32 Dementia & Cognitive Decline Geriatric

Dementia affects ~6.7 million Americans ≥65. Alzheimer's disease accounts for 60-80% of cases, followed by vascular dementia (10-20%), Lewy body dementia (5-15%), and frontotemporal dementia (5-10%). Family physicians are typically the first to identify cognitive decline and initiate the diagnostic workup.

Screening & Diagnosis

MoCA (Montreal Cognitive Assessment): 30-point test covering visuospatial, naming, attention, language, abstraction, delayed recall, and orientation. Score ≤25 suggests cognitive impairment (sensitivity 90%, specificity 87% for MCI). MMSE (Mini-Mental State Exam): 30-point test; ≤23 suggests dementia; less sensitive for MCI than MoCA. Mini-Cog: 3-word recall + clock draw — rapid, effective screen for office use.

Reversible Causes to Exclude

Before diagnosing dementia, rule out: hypothyroidism (TSH), B12 deficiency (serum B12 + methylmalonic acid), depression (pseudodementia) (PHQ-9 — treat depression first and reassess), normal pressure hydrocephalus (triad: magnetic gait, urinary incontinence, dementia — MRI shows ventriculomegaly out of proportion to atrophy), medication effects (anticholinergics, benzodiazepines, opioids), sleep disorders (OSA), syphilis (RPR if risk factors). Standard labs: CBC, CMP, TSH, B12, folate, RPR, urinalysis. MRI brain without contrast to assess for structural causes, vascular changes, and atrophy pattern.

Pharmacotherapy

AgentMechanismIndicationPearl
Donepezil (Aricept) 5-10 mg qhsCholinesterase inhibitorMild-moderate Alzheimer'sMost commonly used; GI side effects, bradycardia; check HR before starting
Rivastigmine (Exelon) patch 4.6-13.3 mg/24hrCholinesterase inhibitorMild-moderate Alzheimer's; Parkinson's disease dementiaPatch formulation reduces GI side effects
Memantine (Namenda) 5-20 mg/dayNMDA receptor antagonistModerate-severe Alzheimer's (often added to donepezil)Better tolerated than ChEIs; may combine with donepezil (Namzaric = combination)
Lecanemab (Leqembi)Anti-amyloid monoclonal antibodyEarly Alzheimer's with confirmed amyloid pathology27% slowing of cognitive decline; ARIA (amyloid-related imaging abnormalities) risk — requires MRI monitoring; IV infusion q2 weeks

Non-pharmacologic management (often more impactful): Structured daily routines, caregiver education and support, safety assessments (driving, wandering, firearms), advance care planning, adult day programs, occupational therapy, music/art therapy, exercise (30+ min walking has cognitive benefits), management of behavioral symptoms (redirect, validate, minimize triggers before using antipsychotics — which carry a black box warning for increased mortality in elderly with dementia).

33 Falls Prevention Geriatric

Falls are the leading cause of injury-related death in adults ≥65 (36,000 deaths/year in the US). One in four older adults falls each year, and falls are the most common cause of traumatic brain injury and hip fracture in this population. The USPSTF recommends exercise interventions to prevent falls in community-dwelling adults ≥65 at increased fall risk (Grade B).

Fall Risk Assessment — Key Components

Screening: Ask every patient ≥65 at annual visit: "Have you fallen in the past year? Do you feel unsteady when standing or walking?" If yes to either → comprehensive fall risk assessment.

Assessment: (1) Gait and balance testing: Timed Up and Go (TUG) — >12 seconds = increased fall risk; 30-second Chair Stand Test. (2) Medication review: target benzodiazepines, opioids, anticholinergics, antihypertensives (orthostatic hypotension), antihistamines. (3) Orthostatic vitals: BP lying → standing at 1 and 3 minutes; drop ≥20 systolic or ≥10 diastolic = orthostatic hypotension. (4) Vision: visual acuity, cataract evaluation. (5) Footwear and home safety: grab bars, remove throw rugs, adequate lighting, non-slip mats. (6) Vitamin D: supplement 800-1000 IU daily (prevents falls via improved muscle strength and neuromuscular function).

Exercise interventions: Tai chi (strongest evidence — reduces falls by 20-30%), balance training, strength training (especially lower extremity), and gait training. Referral to physical therapy for individualized fall prevention program.

34 Advanced Care Planning Geriatric

Advanced care planning (ACP) is the process of discussing and documenting a patient's values, goals, and preferences for future medical care in the event they cannot speak for themselves. Every adult — especially those ≥65 or with serious illness — should have ACP documented. Family physicians are the ideal provider for these conversations because of the longitudinal patient relationship.

Key ACP Documents

DocumentFunctionKey Points
Advance Directive (Living Will)Specifies what treatments the patient does or does not wantCPR, intubation/mechanical ventilation, artificial nutrition/hydration, dialysis; should specify under what conditions (e.g., "if permanently unconscious")
Durable Power of Attorney for Healthcare (Healthcare Proxy)Designates a person to make medical decisions if the patient cannotThe most important ACP document — a named decision-maker who knows the patient's values can address unforeseen scenarios that a living will cannot anticipate
POLST/MOLSTPhysician/Medical Orders for Life-Sustaining TreatmentActionable medical orders (not just patient preferences); signed by physician; honored by EMS; covers CPR, intubation, hospital transfer, IV fluids, antibiotics
DNR/DNIDo Not Resuscitate / Do Not Intubate ordersSpecific medical orders; patients often conflate DNR with "do nothing" — clarify that DNR means no CPR/defibrillation but all other care continues
ACP conversations are not about paperwork — they are about understanding what matters to the patient. The best opening question is not "Do you want CPR?" but "What does a good day look like for you?" or "If you got sicker, what abilities are so important that you couldn't imagine living without them?" This values-based approach produces decisions that are more consistent and less likely to cause family conflict.

35 Common Rashes — Eczema, Psoriasis, Fungal Derm

Atopic Dermatitis (Eczema)

Chronic, relapsing, intensely pruritic dermatitis. Affects 10-20% of children and 1-3% of adults. Distribution varies by age: infants (face, extensor surfaces), children/adults (flexural areas — antecubital fossa, popliteal fossa, neck). Part of the atopic triad (eczema, asthma, allergic rhinitis). Pathophysiology: filaggrin gene mutations lead to epidermal barrier dysfunction + Th2-mediated inflammation.

Management: (1) Restore skin barrier: liberal emollient application (CeraVe, Vanicream, Aquaphor — apply within 3 minutes of bathing). (2) Mild: low-potency topical corticosteroid (hydrocortisone 2.5% for face/folds). (3) Moderate: medium-potency (triamcinolone 0.1% for body). (4) Severe or steroid-sparing: topical calcineurin inhibitors (tacrolimus 0.03-0.1%, pimecrolimus 1%) — no skin atrophy risk. (5) Refractory: dupilumab (Dupixent) — IL-4/IL-13 monoclonal antibody, SC q2wk, approved for ≥6 months. Avoid triggers: fragrances, harsh soaps, wool, dust mites, pet dander. Bleach baths (1/4 cup per full tub, 10 min, 2-3x/week) reduce skin Staph colonization.

Psoriasis

Chronic autoimmune disease affecting 2-3% of the global population. Classic presentation: well-demarcated, salmon-pink plaques with silvery-white scale on extensor surfaces (elbows, knees), scalp, and lumbosacral area. Auspitz sign (pinpoint bleeding when scale is removed). Associated with: psoriatic arthritis (up to 30% of psoriasis patients), metabolic syndrome, depression, cardiovascular disease.

Management by severity: Mild (<3% BSA): topical corticosteroids (betamethasone 0.05% ointment), topical vitamin D analogs (calcipotriene), combination calcipotriene/betamethasone (Enstilar foam). Moderate-severe (>3% BSA or refractory): phototherapy (narrowband UVB), or systemic agents: methotrexate 7.5-25 mg/week (monitor LFTs, CBC; avoid in liver disease/pregnancy), apremilast (Otezla — PDE4 inhibitor), or biologics (adalimumab/Humira, secukinumab/Cosentyx, risankizumab/Skyrizi, guselkumab/Tremfya). Screen for psoriatic arthritis (morning stiffness, dactylitis, nail pitting) at every visit.

Dermatophyte Infections (Tinea)

TypeLocationAppearanceTreatment
Tinea corporis (ringworm)Body/trunkAnnular, erythematous, scaly plaque with central clearingTopical: terbinafine 1% BID or clotrimazole 1% BID × 2-4 weeks
Tinea pedis (athlete's foot)Feet (interdigital, moccasin, vesicular)Scaling, maceration, fissuring between toes; or diffuse scaling of soleTopical antifungal × 4 weeks; keep feet dry
Tinea cruris (jock itch)Groin, inner thighErythematous, scaly plaques with raised border; spares scrotum (unlike candida)Topical antifungal × 2-4 weeks; powder to reduce moisture
Tinea capitisScalp (children)Scaly patches with hair loss, "black dot" tinea, kerion (boggy, inflammatory mass)SYSTEMIC required (topicals don't penetrate hair follicle): griseofulvin 20-25 mg/kg/day × 6-8 weeks or terbinafine 250 mg/day × 4-6 weeks (adults/older children)
Tinea unguium (onychomycosis)Nails (toenails > fingernails)Thickened, yellow, brittle, dystrophic nails; subungual debrisTerbinafine (Lamisil) 250 mg daily × 6 weeks (fingernails) or 12 weeks (toenails); check LFTs; topical efinaconazole (Jublia) for mild cases
KOH prep is the office diagnostic test for dermatophytes: scrape the leading edge of the lesion onto a slide, add KOH 10-20%, gently heat, look under microscope for septate branching hyphae. This takes 2 minutes and confirms the diagnosis before prescribing antifungals — important because eczema nummulare, contact dermatitis, and granuloma annulare can mimic tinea corporis.
Photograph of psoriatic plaques on the back showing well-demarcated erythematous lesions with silvery scale
Figure 11 — Psoriasis. Well-demarcated erythematous plaques with characteristic silvery-white scale on the trunk. Psoriasis is a T-cell mediated autoimmune disease with systemic inflammatory consequences. Source: Wikimedia Commons, by Eisfelder. Licensed under CC BY-SA 3.0.

36 Skin Cancer Screening (ABCDE) Derm

Melanoma accounts for only 1% of skin cancers but causes the majority of skin cancer deaths (~8,000/year in the US). Family physicians perform opportunistic skin cancer screening during physical exams — the USPSTF has an I (insufficient evidence) rating for routine whole-body screening in asymptomatic average-risk adults, but clinical vigilance remains essential.

ABCDE Criteria for Melanoma

CriterionFeatureDetail
A — AsymmetryOne half unlike the otherBenign nevi are symmetric
B — BorderIrregular, ragged, notched, or blurred edgesBenign nevi have smooth, even borders
C — ColorVaried (brown, black, red, white, blue within one lesion)Benign nevi are usually one shade of brown
D — Diameter>6 mm (pencil eraser)Though melanomas can be smaller; diameter alone is not sensitive
E — EvolvingChanging in size, shape, color, or new symptoms (bleeding, itching)Most important criterion; any changing mole in an adult warrants evaluation

The "ugly duckling" sign: A mole that looks different from all other moles on the patient's body — even if it doesn't meet ABCDE criteria — warrants biopsy. This is often how nodular melanoma (which may be symmetric and uniform) is caught.

Non-Melanoma Skin Cancers

Basal cell carcinoma (BCC): Most common cancer in humans. Pearly, translucent papule/nodule with telangiectasia and rolled borders; may have central ulceration ("rodent ulcer"). Sun-exposed areas. Locally invasive but almost never metastasizes. Treatment: excision, Mohs surgery (face/high-risk), ED&C, topical imiquimod (superficial BCC).

Squamous cell carcinoma (SCC): Keratotic papule/plaque, may be ulcerated, on sun-exposed skin (especially scalp, ears, lower lip, dorsal hands). Can metastasize (2-6% risk, higher on lip/ear, immunosuppressed patients). Precursor: actinic keratosis (scaly, rough papule on sun-damaged skin — treat with cryotherapy, topical 5-FU, or imiquimod). SCC treatment: excision with margins, Mohs for high-risk.

Clinical photograph of a melanoma showing asymmetry, irregular borders, and color variation
Figure 12 — Melanoma. This lesion demonstrates multiple ABCDE criteria: asymmetry, irregular borders, color variation (dark brown, light brown, black areas), and diameter >6 mm. Any suspicious lesion should undergo excisional biopsy with narrow margins. Source: Wikimedia Commons. Public domain / NCI.

37 Acne Derm

Acne vulgaris affects 85% of adolescents and can persist into adulthood. Pathophysiology involves four mechanisms: (1) follicular hyperkeratinization (plugging), (2) excess sebum production (androgen-driven), (3) Cutibacterium acnes (formerly Propionibacterium acnes) proliferation, (4) inflammation. Classification: comedonal (whiteheads/blackheads), inflammatory (papules, pustules), nodulocystic (deep, painful nodules/cysts — highest scarring risk).

Treatment by Severity

SeverityFirst-LineAdd-On / Second-LinePearl
Mild comedonalTopical retinoid (adapalene 0.1% / Differin — OTC, tretinoin 0.025-0.1%)Benzoyl peroxide (BP) 2.5-5% — antibacterialRetinoids are the backbone of ALL acne regimens — they normalize follicular keratinization
Mild-moderate inflammatoryTopical retinoid + topical BP ± topical antibiotic (clindamycin 1%)Combination products: adapalene/BP (Epiduo), clindamycin/BP (Duac)NEVER use topical antibiotics as monotherapy (resistance); always combine with BP
Moderate-severe inflammatoryOral antibiotic (doxycycline 100 mg daily or minocycline 100 mg daily) + topical retinoid + BPOral antibiotics × 3 months max then discontinue (maintain with topicals); spironolactone 50-200 mg daily in women (anti-androgen)Limit oral antibiotic duration to prevent resistance; combine with topical regimen always
Severe nodulocystic or refractoryIsotretinoin (Accutane) 0.5-1 mg/kg/day × 15-20 weeks (cumulative dose 120-150 mg/kg)iPLEDGE program required (teratogenicity — pregnancy test monthly, 2 forms of contraception); monitor LFTs, lipids monthly; dry skin/lips universal; depression monitoring (causal link debated)

38 Joint Injections Procedure

Corticosteroid injections are among the most commonly performed office procedures in family medicine. Indications: inflammatory or degenerative joint pain refractory to oral management, bursitis, trigger finger, de Quervain's tenosynovitis, plantar fasciitis.

Common Injection Sites & Technique

Joint/SiteApproachSteroid / DosePearl
KneeSuperolateral (most common): patient supine, knee extended, insert needle at superolateral patellar border directed under patellaTriamcinolone 40 mg + 3-5 mL lidocaine 1%Aspirate effusion first (send for cell count, crystals, culture if infection suspected); limit to 3-4 injections/year
Shoulder (subacromial)Posterior approach: 2 cm inferior and medial to posterolateral acromion corner; direct needle anteriorly and slightly superiorly into subacromial spaceTriamcinolone 40 mg + 3-5 mL lidocaine 1%Pain relief confirms impingement diagnosis (diagnostic + therapeutic)
Trigger finger (A1 pulley)Insert needle at palmar MCP crease, tangential to tendon, into tendon sheathTriamcinolone 10 mg + 0.5 mL lidocaine 1%Single injection resolves ~60-70% of trigger fingers; may repeat once before surgical referral
Lateral epicondyle (tennis elbow)Palpate maximally tender point at lateral epicondyle; insert perpendicular to skinTriamcinolone 10-20 mg + 1 mL lidocaine 1%Short-term relief but may worsen long-term outcomes vs PT alone; use judiciously
Greater trochanteric bursaLateral decubitus; palpate maximal tenderness over greater trochanter; insert perpendicularTriamcinolone 40 mg + 3-5 mL lidocaine 1%Combined injection + PT has best outcomes
Always document: informed consent, site and side, sterile technique, needle gauge and length, medication and dose injected, amount of fluid aspirated (if applicable), post-procedure instructions (rest joint 24-48 hr, ice, avoid heavy use for 72 hr), and follow-up plan. Contraindications: active joint infection (septic arthritis), overlying skin infection, coagulopathy (relative), prosthetic joint (relative — send to orthopedics).
Lateral view diagram of knee joint anatomy showing the joint space, patella, femur, and tibia
Figure 13 — Knee Joint Anatomy. Understanding the anatomy of the knee joint — including the suprapatellar pouch, joint line, and surrounding bursae — is essential for accurate intra-articular injection. Source: Wikimedia Commons, by BruceBlaus. Licensed under CC BY 3.0.

39 Skin Biopsy & Excision Procedure

Family physicians perform the majority of skin biopsies in the US. The three main biopsy types serve different diagnostic purposes:

TechniqueMethodBest ForPearl
Shave biopsyTangential excision with blade or DermaBlade parallel to skin surfaceRaised lesions, superficial lesions; when melanoma is NOT suspectedFastest, minimal scarring; does NOT provide depth — never use for pigmented lesions suspicious for melanoma
Punch biopsyCircular blade (2-6 mm) through full thickness of skinInflammatory rashes (need epidermis + dermis for path), alopecia, small lesions; can be diagnostic or excisional if ≤4 mmStandard: 4 mm punch for most indications; 1-2 sutures to close; orient punch along relaxed skin tension lines (RSTL) for best cosmetic result
Excisional biopsyElliptical excision with scalpel, full thickness including subcutaneous fatSuspected melanoma (need full depth + margins), lipomas, cysts, any lesion requiring complete removal3:1 length-to-width ellipse ratio; orient along RSTL; for suspected melanoma: 1-3 mm clinical margins at biopsy; definitive wide excision with margins based on Breslow depth after pathology

Local anesthesia: Lidocaine 1% (max dose 4.5 mg/kg without epi, 7 mg/kg with epi). Buffer with sodium bicarbonate (1 mL bicarb per 9 mL lidocaine) to reduce injection pain. Inject slowly, use small-gauge needle (27-30G). Avoid epinephrine on digits (historic teaching, now debated — low-dose epinephrine on fingers is increasingly considered safe).

40 Spirometry Procedure

Spirometry is the office-based pulmonary function test used to diagnose and monitor obstructive lung diseases (asthma, COPD). Every family medicine office should have the capability to perform spirometry.

Key Spirometry Values

MeasureDefinitionClinical Significance
FEV1Forced expiratory volume in 1 secondMost reproducible measure; used to grade COPD severity and assess asthma control
FVCForced vital capacity — total volume exhaled after maximal inspirationReduced in restrictive disease; may be reduced in severe obstruction (air trapping)
FEV1/FVC ratioProportion of FVC exhaled in first second<0.70 = obstruction (GOLD criteria for COPD). Normal for age needed — ratio naturally decreases with age
Bronchodilator responseRepeat spirometry 15-20 min after 400 mcg albuterol≥12% AND ≥200 mL improvement in FEV1 = positive (reversible obstruction — suggests asthma)

GOLD COPD Staging by FEV1 (Post-Bronchodilator)

StageFEV1 (% predicted)Severity
GOLD 1≥80%Mild
GOLD 250-79%Moderate
GOLD 330-49%Severe
GOLD 4<30%Very severe

COPD maintenance therapy (GOLD 2024): All: smoking cessation + influenza/pneumococcal/COVID vaccination + pulmonary rehab. Group A (few symptoms, low exacerbation risk): SABA or SAMA PRN. Group B (more symptoms): LABA or LAMA (tiotropium/Spiriva is most studied LAMA). Group E (exacerbations): LABA + LAMA; if eosinophils ≥300: LABA + LAMA + ICS (triple therapy — ETHOS and IMPACT trials showed mortality benefit).

Spirometry flow-volume loop comparing normal pattern with obstructive pattern showing scooped expiratory limb
Figure 14 — Spirometry Patterns. Normal spirometry (left) compared with obstructive pattern (right) showing reduced FEV1, scooped expiratory limb, and reduced FEV1/FVC ratio — characteristic of COPD or asthma. Source: Wikimedia Commons. Public domain.

41 Wound Care Procedure

Laceration repair and wound management are core family medicine procedures. The two critical decisions: (1) Does this wound need closure? (2) Primary (sutures/staples now), delayed primary (close in 3-5 days if contaminated), or secondary intention (leave open to heal by granulation)?

Wound Closure Guidelines

FactorPrimary Closure AppropriateDelayed or Secondary Closure
Time since injury<6-8 hours (body), <12-24 hours (face — rich blood supply)>24 hours, or grossly contaminated
ContaminationClean or minimally contaminatedHeavy contamination, bite wounds (except face), soil/organic matter
MechanismSharp/clean lacerationCrush injury, stellate laceration, high-velocity projectile

Suture selection: Face: 5-0 or 6-0 non-absorbable (nylon), remove in 5 days. Scalp: staples (fast, effective) or 3-0 nylon, remove in 7-10 days. Extremity: 4-0 nylon, remove in 10-14 days. Deep layer (dermal): absorbable (Vicryl 4-0 or 5-0) for tension reduction — buried knot. Tissue adhesive (Dermabond): appropriate for clean, low-tension lacerations, especially in children.

Tetanus prophylaxis: Clean minor wound: Tdap/Td if >10 years since last dose. All other wounds (contaminated, puncture, crush, burns, frostbite): Tdap/Td if >5 years since last dose. If unknown or <3 prior doses: give Tdap + TIG (tetanus immune globulin) for non-clean wounds.

42 Splinting & Fracture Management Procedure

Family physicians diagnose and initially manage the majority of non-displaced fractures. Proper splinting immobilizes the injured area, reduces pain, and prevents further injury during the healing process.

Splinting Principles

Immobilize one joint above and one joint below the fracture. Apply over appropriate padding (stockinette + cotton roll/Webril). Check and document neurovascular status (sensation, capillary refill, pulses) before AND after splint application. Common splints:

Splint TypeIndicationPosition
Sugar-tong forearmDistal radius fractures (Colles', Smith's)Elbow 90° flexion, wrist neutral to slight extension
Ulnar gutter4th/5th metacarpal fractures (Boxer's fracture)Wrist 20-30° extension, MCP 70-90° flexion, IP joints slightly flexed
Thumb spicaScaphoid fracture (snuffbox tenderness), De Quervain's, thumb UCL injury (gamekeeper's)Wrist neutral, thumb in abduction (glass-holding position)
Posterior ankleAnkle fractures (non-displaced), severe sprainsAnkle 90° (neutral dorsiflexion), toes free
Buddy tapingNon-displaced phalangeal fractures, finger sprainsTape injured finger to adjacent finger with gauze between; allows some ROM

Ottawa Ankle Rules: X-ray only if: bone tenderness at posterior edge or tip of lateral or medial malleolus, OR inability to bear weight immediately and in the ED (4 steps). These rules have ~98% sensitivity for fracture and reduce unnecessary X-rays by 30-40%. Similar rules exist for knee (Ottawa Knee Rules) and foot (Ottawa Foot Rules for midfoot fractures).

Scaphoid fractures are the most commonly missed fracture in primary care. Clinical scenario: fall on outstretched hand (FOOSH), anatomic snuffbox tenderness, negative initial X-ray. If high clinical suspicion: treat as scaphoid fracture (thumb spica splint), repeat X-ray in 10-14 days (fracture line becomes visible as bone resorbs), or obtain MRI for early diagnosis. Missed scaphoid fractures can lead to avascular necrosis due to the bone's retrograde blood supply.

43 USPSTF Screening Guidelines — Consolidated

ConditionPopulationScreening MethodIntervalGrade
HypertensionAdults ≥18Office BPAnnual; q3-5yr if normal <40A
Type 2 DiabetesAdults 35-70 with overweight/obesityFPG, A1C, or OGTTEvery 3 yearsB
DyslipidemiaMen ≥35; women ≥45Lipid panelEvery 5 yearsA/B
Colorectal CancerAdults 45-75Colonoscopy, FIT, CologuardDepends on modalityA
Breast CancerWomen 40-74MammographyBiennialB
Cervical CancerWomen 21-65Pap ± hrHPVq3-5yr depending on testA
Lung CancerAdults 50-80, ≥20 pack-year hxLow-dose CTAnnualB
AAAMen 65-75 who ever smokedAbdominal USOne-timeB
OsteoporosisWomen ≥65; postmenopausal <65 with riskDEXAPer riskB
DepressionAll adults ≥18PHQ-2/PHQ-9AnnualB
Hepatitis CAdults 18-79Anti-HCV AbOne-timeB
HIVAdults 15-65HIV Ag/AbAt least onceA
Hepatitis BAdolescents/adults at increased riskHBsAg, anti-HBs, anti-HBcPer riskB
STIs (Chlamydia/Gonorrhea)Sexually active women <25, others at riskNAATAnnualB
Prediabetes/DM (pregnancy)Pregnant women 24-28 wkGCT/OGTT24-28 weeksB
Unhealthy Alcohol UseAdults ≥18AUDIT-CAnnualB
Tobacco UseAll adultsAsk + advise cessationEvery visitA
ObesityAdults ≥18BMI calculationAnnualB
AnxietyAdults <65GAD-7Per clinical judgmentB

44 Classification Systems

SystemApplicationKey Features
JNC 8 / 2017 ACC/AHA BP ClassificationHypertension stagingNormal, Elevated, Stage 1 (130-139/80-89), Stage 2 (≥140/90), Crisis (>180/120)
ADA Diabetes CriteriaDiabetes diagnosisFPG ≥126, 2-hr OGTT ≥200, A1C ≥6.5%, random glucose ≥200 + symptoms
BMI Classification (WHO)Obesity stagingUnderweight <18.5, Normal 18.5-24.9, Overweight 25-29.9, Obesity I/II/III: 30/35/40+
Centor / McIsaac ScorePharyngitis — strep likelihood5 criteria (exudate, LAD, fever, no cough, age); guides testing/treatment
CURB-65Pneumonia severityConfusion, Urea >7, RR ≥30, BP <90/60, age ≥65; 0-1 outpatient, 2 consider admit, 3+ ICU
PHQ-9Depression severity0-4 minimal, 5-9 mild, 10-14 moderate, 15-19 mod-severe, 20-27 severe
GAD-7Anxiety severity0-4 minimal, 5-9 mild, 10-14 moderate, 15-21 severe
AUDIT / AUDIT-CAlcohol use screeningAUDIT-C ≥4 (men) / ≥3 (women) = positive screen
Kellgren-LawrenceOA radiographic severityGrades 0-4: normal to severe (osteophytes, narrowing, sclerosis, deformity)
T-Score (WHO)Bone densityNormal ≥−1.0, Osteopenia −1.0 to −2.5, Osteoporosis ≤−2.5
BI-RADSMammography assessmentCategories 0-6: incomplete to known malignancy
Bethesda SystemPap smear cytologyNILM, ASC-US, ASC-H, LSIL, HSIL, AGC, carcinoma
GOLD StagingCOPD severity1-4 by FEV1 % predicted: ≥80, 50-79, 30-49, <30
NYHA Functional ClassHeart failure severityI (no limitation), II (slight), III (marked), IV (symptoms at rest)
CKD Staging (KDIGO)Chronic kidney diseaseStages 1-5 by eGFR: ≥90, 60-89, 30-59, 15-29, <15
ASCVD Risk (PCE)10-year CV riskLow <5%, Borderline 5-7.4%, Intermediate 7.5-19.9%, High ≥20%
Ottawa RulesAnkle/knee/foot X-ray decisionClinical criteria to rule out fracture without imaging; ~98% sensitivity
Beers Criteria (AGS)Potentially inappropriate medications in elderlyUpdated every 3 years; categorizes drugs to avoid, use with caution, or avoid in specific conditions

45 Medications Master Table

Antihypertensives

Generic (Brand)ClassTypical DoseMechanismKey Pearl
Lisinopril (Zestril)ACEi10-40 mg daily↓ Angiotensin IICough 10-20%; angioedema; monitor K+/Cr; CI in pregnancy
Losartan (Cozaar)ARB50-100 mg dailyAT1 receptor blockadeNo cough; uricosuric effect (lowers uric acid)
Amlodipine (Norvasc)DHP-CCB5-10 mg dailyVascular smooth muscle relaxationPeripheral edema; long half-life; safe in pregnancy (category C)
ChlorthalidoneThiazide-like12.5-25 mg daily↓ NaCl reabsorption in DCTMore potent than HCTZ; hypokalemia, hyponatremia, hyperuricemia
Metoprolol succinate (Toprol XL)Beta-1 selective blocker25-200 mg daily↓ HR and contractilityAlso for HFrEF; avoid abrupt discontinuation; mask hypoglycemia in diabetics
Spironolactone (Aldactone)MRA25-50 mg dailyAldosterone antagonismBest 4th-line for resistant HTN; hyperkalemia; gynecomastia in men

Diabetes Agents

Generic (Brand)ClassTypical DoseA1C ReductionKey Pearl
Metformin (Glucophage)Biguanide500-2000 mg daily1.0-1.5%First-line; hold if eGFR <30; GI side effects → use ER
Semaglutide (Ozempic)GLP-1 RA0.25-2 mg SC weekly1.0-1.8%CV benefit; weight loss; nausea; CI with MTC/MEN2
Empagliflozin (Jardiance)SGLT2i10-25 mg daily0.5-0.9%CV + renal + HF benefit; genital mycotic infections; euglycemic DKA
Glipizide (Glucotrol)Sulfonylurea5-20 mg daily1.0-1.5%Cheap; hypoglycemia risk; weight gain
Sitagliptin (Januvia)DPP-4i100 mg daily0.5-0.8%Weight-neutral; dose adjust for CKD; no CV benefit
Insulin glargine (Lantus)Basal insulin10 U → titrate1.5-3.5%Start 10 U or 0.1-0.2 U/kg; titrate by 2 U q3d to fasting target

Lipid Agents

Generic (Brand)ClassTypical DoseLDL ReductionKey Pearl
Atorvastatin (Lipitor)HMG-CoA reductase inhibitor10-80 mg daily30-50%+ (dose-dependent)High-intensity at 40-80 mg; myalgias 5-10%; hepatotoxicity rare; check baseline LFTs
Rosuvastatin (Crestor)Statin5-40 mg daily30-50%+Most potent statin per mg; high-intensity at 20-40 mg; CKD dose adjustment
Ezetimibe (Zetia)Cholesterol absorption inhibitor10 mg daily~18%Add-on to statin; IMPROVE-IT trial: benefit in ACS patients
Icosapent ethyl (Vascepa)Omega-3 (EPA)2 g BIDTG reduction; CV risk reductionREDUCE-IT: 25% CV event reduction; use with statin; AFib risk
Evolocumab (Repatha)PCSK9 inhibitor140 mg SC q2wk~60%For ASCVD patients not at LDL goal on max statin + ezetimibe; expensive

Antibiotics (Common Primary Care)

Generic (Brand)ClassCommon UseKey Pearl
AmoxicillinAminopenicillinStrep pharyngitis, AOM, sinusitisFirst-line for many pediatric infections; 80-90 mg/kg/day for AOM
Amoxicillin-clavulanate (Augmentin)Beta-lactam + BLISinusitis, AOM (2nd-line), bite woundsCovers beta-lactamase producers; diarrhea common
Azithromycin (Zithromax)MacrolideCAP, chlamydia, pertussis5-day Z-pack; QTc prolongation; increasing resistance in S. pneumoniae
DoxycyclineTetracyclineSinusitis (alt), cellulitis (MRSA), Lyme, chlamydia, acnePhotosensitivity; esophageal erosion (take with water, upright); avoid in children <8 and pregnancy
Cephalexin (Keflex)1st gen cephalosporinCellulitis (non-purulent), UTI (pregnancy)MSSA coverage; does not cover MRSA
TMP-SMX (Bactrim DS)Folate antagonistUTI, MRSA skin infectionsCheck sulfa allergy; hyperkalemia; avoid in 3rd trimester
Nitrofurantoin (Macrobid)NitrofuranUncomplicated cystitisFirst-line UTI; avoid if eGFR <30; does not treat pyelonephritis
Ciprofloxacin (Cipro)FluoroquinolonePyelonephritis, complicated UTIFDA black box: tendon rupture, aortic dissection, neuropathy; reserve for serious infections

Mental Health Medications

Generic (Brand)ClassTypical DoseKey Pearl
Sertraline (Zoloft)SSRI50-200 mg dailyFirst-line MDD/GAD/PTSD/OCD/panic; safest in cardiac patients
Escitalopram (Lexapro)SSRI10-20 mg dailyBest tolerated; fewest interactions; QTc at 20 mg
Bupropion XL (Wellbutrin)NDRI150-450 mg dailyNo sexual dysfunction/weight gain; CI in seizures/eating disorders
Duloxetine (Cymbalta)SNRI30-120 mg dailyMDD + pain; hepatotoxicity with alcohol; nausea
Buspirone (BuSpar)5-HT1A agonist10-30 mg BID-TIDNon-addictive anxiolytic; 2-4 week onset; no CNS depression
Methylphenidate ER (Concerta)Stimulant18-72 mg dailyADHD first-line; monitor growth, HR, BP; Schedule II
Naltrexone (Vivitrol)Opioid antagonist50 mg PO or 380 mg IM monthlyAUD and OUD; patient must be opioid-free 7-10 days
Buprenorphine-naloxone (Suboxone)Partial mu agonist8-24 mg SL dailyOUD maintenance; X-waiver eliminated 2023; ceiling on respiratory depression

46 Abbreviations Master List

Diagnoses

HTNHypertension DM / T2DMDiabetes mellitus / Type 2 diabetes mellitus DM1Type 1 diabetes mellitus CADCoronary artery disease CHF / HFCongestive heart failure HFrEFHeart failure with reduced ejection fraction HFpEFHeart failure with preserved ejection fraction AFibAtrial fibrillation ASCVDAtherosclerotic cardiovascular disease CKDChronic kidney disease ESRDEnd-stage renal disease COPDChronic obstructive pulmonary disease OSAObstructive sleep apnea GERDGastroesophageal reflux disease PUDPeptic ulcer disease IBDInflammatory bowel disease IBSIrritable bowel syndrome NAFLDNon-alcoholic fatty liver disease OAOsteoarthritis RARheumatoid arthritis DVTDeep vein thrombosis PEPulmonary embolism VTEVenous thromboembolism TIATransient ischemic attack CVACerebrovascular accident (stroke) URIUpper respiratory infection UTIUrinary tract infection AOMAcute otitis media GDMGestational diabetes mellitus PCOSPolycystic ovary syndrome PIDPelvic inflammatory disease BPHBenign prostatic hyperplasia MDDMajor depressive disorder GADGeneralized anxiety disorder PTSDPost-traumatic stress disorder OCDObsessive-compulsive disorder ADHDAttention-deficit/hyperactivity disorder AUDAlcohol use disorder OUDOpioid use disorder SUDSubstance use disorder ASDAutism spectrum disorder SSTISkin and soft tissue infection MRSAMethicillin-resistant Staphylococcus aureus GBSGroup B Streptococcus STISexually transmitted infection

Screening & Assessment Tools

PHQ-9Patient Health Questionnaire-9 (depression) PHQ-2Patient Health Questionnaire-2 (depression screen) GAD-7Generalized Anxiety Disorder-7 AUDIT-CAlcohol Use Disorders Identification Test-Concise MMSEMini-Mental State Examination MoCAMontreal Cognitive Assessment ASQ-3Ages and Stages Questionnaire (developmental screen) M-CHATModified Checklist for Autism in Toddlers FRAXFracture Risk Assessment Tool COWSClinical Opiate Withdrawal Scale STOP-BANGOSA screening questionnaire HEEADSSSAdolescent psychosocial assessment (Home, Education, Eating, Activities, Drugs, Sexuality, Suicide, Safety) SBIRTScreening, Brief Intervention, Referral to Treatment

Procedures & Imaging

I&DIncision and drainage LEEPLoop electrosurgical excision procedure IUDIntrauterine device DEXADual-energy X-ray absorptiometry CXRChest X-ray CTComputed tomography MRIMagnetic resonance imaging USUltrasound ECG/EKGElectrocardiogram FITFecal immunochemical test NAATNucleic acid amplification test RADTRapid antigen detection test OGTTOral glucose tolerance test GCTGlucose challenge test LDCTLow-dose computed tomography

Medications & Labs

SSRISelective serotonin reuptake inhibitor SNRISerotonin-norepinephrine reuptake inhibitor TCATricyclic antidepressant NSAIDNon-steroidal anti-inflammatory drug PPIProton pump inhibitor ACEiAngiotensin-converting enzyme inhibitor ARBAngiotensin receptor blocker CCBCalcium channel blocker GLP-1 RAGlucagon-like peptide-1 receptor agonist SGLT2iSodium-glucose cotransporter 2 inhibitor DPP-4iDipeptidyl peptidase-4 inhibitor ICSInhaled corticosteroid LABALong-acting beta agonist LAMALong-acting muscarinic antagonist SABAShort-acting beta agonist NRTNicotine replacement therapy MATMedication-assisted treatment LARCLong-acting reversible contraception OCPOral contraceptive pill CHCCombined hormonal contraceptive HT/HRTHormone therapy / hormone replacement therapy DMPADepot medroxyprogesterone acetate A1CHemoglobin A1C (glycated hemoglobin) LDLLow-density lipoprotein HDLHigh-density lipoprotein TGTriglycerides eGFREstimated glomerular filtration rate UACRUrine albumin-to-creatinine ratio TSHThyroid-stimulating hormone CBCComplete blood count CMPComprehensive metabolic panel LFTsLiver function tests ESRErythrocyte sedimentation rate CRPC-reactive protein MMEMorphine milligram equivalents PDMPPrescription drug monitoring program

Organizations & Guidelines

USPSTFUS Preventive Services Task Force ACIPAdvisory Committee on Immunization Practices AAPAmerican Academy of Pediatrics ADAAmerican Diabetes Association AHAAmerican Heart Association ACCAmerican College of Cardiology AAFPAmerican Academy of Family Physicians ACOGAmerican College of Obstetricians and Gynecologists CDCCenters for Disease Control and Prevention GOLDGlobal Initiative for Chronic Obstructive Lung Disease ASCCPAmerican Society for Colposcopy and Cervical Pathology AGSAmerican Geriatrics Society

47 Immunization Schedules (Adult & Pediatric)

Adult Immunization Schedule (CDC/ACIP)

VaccineIndicationSchedulePearl
InfluenzaAll adults annually1 dose annually (fall)Egg allergy no longer a contraindication (even with anaphylaxis); high-dose (Fluzone HD) or adjuvanted (Fluad) for ≥65
Td/TdapAll adultsTdap once (if not received), then Td or Tdap q10 yearsTdap during each pregnancy (27-36 weeks) regardless of prior vaccination
COVID-19All adultsPer current CDC recommendations (updated annually)Updated formulations target circulating variants; coadministration with other vaccines is acceptable
Shingles (Shingrix)Adults ≥502 doses, 2-6 months apartRecombinant (not live); 90%+ efficacy; give even if prior Zostavax or prior shingles episode
Pneumococcal (PCV20 or PCV15+PPSV23)Adults ≥65, or 19-64 with risk factorsPCV20 single dose (preferred); or PCV15 → PPSV23 ≥1 year laterRisk factors: chronic heart/lung/liver/kidney disease, diabetes, alcoholism, smoking, immunocompromised, CSF leak, cochlear implant
Hepatitis BAdults 19-59 (all); ≥60 with risk factors3-dose (Engerix-B: 0, 1, 6 months) or 2-dose (Heplisav-B: 0, 1 month)Heplisav-B preferred for rapid completion; check anti-HBs 1-2 months after completion in healthcare workers and dialysis patients
HPV (Gardasil 9)Through age 26 (routine); 27-45 shared decision-making2 doses (if started <15) or 3 dosesCatch-up through 26; most effective before sexual debut; prevents 6 cancer types
MMRAdults born after 1957 without evidence of immunity1 or 2 doses depending on risk (healthcare workers, international travel: 2 doses)Live vaccine; CI in pregnancy and severe immunodeficiency
VaricellaAdults without evidence of immunity2 doses, 4-8 weeks apartLive vaccine; CI in pregnancy; evidence of immunity = US-born before 1980, documented doses, positive titer, or provider-diagnosed disease
RSV (Abrysvo or Arexvy)Adults ≥60 (shared decision-making); pregnant persons 32-36 weeks (Abrysvo)Single doseNew (2023); seasonal (fall); maternal vaccination protects newborns from RSV bronchiolitis
Healthcare worker administering an intramuscular vaccine to a child's arm
Figure 15 — Childhood Vaccination. Immunization is the most effective preventive intervention in pediatric primary care, preventing approximately 42,000 deaths per year in the US. Source: Wikimedia Commons. Public domain.

References & Figure Sources

Figures

  1. Figure 1 — The Stethoscope. Wikimedia Commons. Public domain.
  2. Figure 2 — Physical Examination. Wikimedia Commons. Public domain.
  3. Figure 3 — Blood Pressure Measurement. Wikimedia Commons. Public domain.
  4. Figure 4 — Hypertension Pathophysiology. BruceBlaus. Wikimedia Commons. Licensed under CC BY 3.0.
  5. Figure 5 — Type 2 Diabetes Pathophysiology. BruceBlaus. Wikimedia Commons. Licensed under CC BY 3.0.
  6. Figure 6 — Acute Otitis Media. B. Welleschik. Wikimedia Commons. Licensed under CC BY-SA 3.0.
  7. Figure 7 — Serotonin Structure. Wikimedia Commons. Public domain.
  8. Figure 8 — Intrauterine Device (IUD). BruceBlaus. Wikimedia Commons. Licensed under CC BY 3.0.
  9. Figure 9 — Mammography. Wikimedia Commons. Public domain.
  10. Figure 10 — Well-Child Growth Assessment. Wikimedia Commons. Public domain.
  11. Figure 11 — Psoriasis. Eisfelder. Wikimedia Commons. Licensed under CC BY-SA 3.0.
  12. Figure 12 — Melanoma. NCI. Wikimedia Commons. Public domain.
  13. Figure 13 — Knee Joint Anatomy. BruceBlaus. Wikimedia Commons. Licensed under CC BY 3.0.
  14. Figure 14 — Spirometry Patterns. Wikimedia Commons. Public domain.
  15. Figure 15 — Childhood Vaccination. Wikimedia Commons. Public domain.

Key Guidelines & Trials

  1. Whelton PK, Carey RM, Aronow WS, et al. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA Guideline for the Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults. J Am Coll Cardiol. 2018;71(19):e127-e248. PMID: 29133356
  2. SPRINT Research Group. A Randomized Trial of Intensive versus Standard Blood-Pressure Control. N Engl J Med. 2015;373(22):2103-2116. PMID: 26551272
  3. American Diabetes Association Professional Practice Committee. Standards of Care in Diabetes — 2024. Diabetes Care. 2024;47(Suppl 1). PMID: 36507645
  4. Grundy SM, Stone NJ, Bailey AL, et al. 2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Blood Cholesterol. Circulation. 2019;139(25):e1082-e1143. PMID: 30586774
  5. Bhatt DL, Steg PG, Miller M, et al. Cardiovascular Risk Reduction with Icosapent Ethyl for Hypertriglyceridemia (REDUCE-IT). N Engl J Med. 2019;380(1):11-22. PMID: 30415628
  6. Dowell D, Ragan KR, Jones CM, et al. CDC Clinical Practice Guideline for Prescribing Opioids for Pain — United States, 2022. MMWR Recomm Rep. 2022;71(3):1-95. PMID: 36327391
  7. US Preventive Services Task Force. Screening for Prediabetes and Type 2 Diabetes: US Preventive Services Task Force Recommendation Statement. JAMA. 2021;326(8):736-743. PMID: 30763518
  8. Jaddoe VWV, et al. Global Vascular Guidelines reference. Used for ASCVD risk framework. PMID: 31159978
  9. Zinman B, Wanner C, Lachin JM, et al. Empagliflozin, Cardiovascular Outcomes, and Mortality in Type 2 Diabetes (EMPA-REG OUTCOME). N Engl J Med. 2015;373(22):2117-2128. PMID: 26378978
  10. Marso SP, Daniels GH, Poulter NR, et al. Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes (LEADER). N Engl J Med. 2016;375(4):311-322. PMID: 27295427
  11. Williams B, MacDonald TM, Morant SV, et al. Spironolactone versus placebo, bisoprolol, and doxazosin to determine the optimal treatment for drug-resistant hypertension (PATHWAY-2). Lancet. 2015;386(10008):2059-2068. PMID: 26414968

Textbooks & Reference Works

  1. Rakel's Textbook of Family Medicine. 10th ed. Rakel RE, Rakel DP, eds. Elsevier; 2021.
  2. Current Medical Diagnosis & Treatment (CMDT). Papadakis MA, McPhee SJ, eds. McGraw-Hill. Updated annually.
  3. Bright Futures: Guidelines for Health Supervision of Infants, Children, and Adolescents. 4th ed. Hagan JF, Shaw JS, Duncan PM, eds. AAP; 2017.
  4. Pfenninger and Fowler's Procedures for Primary Care. 4th ed. Pfenninger JL, Fowler GC, eds. Elsevier; 2019.