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i have a general medicine exam, for physiotherapy students help me prepare for it I will share the pyq question paper I want you to give me the detail answer for every topic in that paper.

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Here is your complete, detailed exam preparation guide covering every topic from all your PYQ papers. This is organized by topic for easy study.

πŸ₯ GENERAL MEDICINE - COMPLETE PYQ ANSWER GUIDE

For Physiotherapy Students


πŸ“Œ TOPIC 1: URINARY TRACT INFECTION (UTI)

(Repeated in multiple papers - high priority)

Definition

UTI is an infection of any part of the urinary system - kidneys, ureters, bladder, or urethra. It is more common in females due to the shorter urethra.

Classification

  • Upper UTI: Pyelonephritis (kidney infection)
  • Lower UTI: Cystitis (bladder), Urethritis (urethra)
  • Complicated vs Uncomplicated: Complicated = structural/functional abnormality, pregnancy, immunocompromised state

Causes (Organisms)

OrganismFrequency
E. coli80-85% (most common)
Staphylococcus saprophyticusYoung women
Klebsiella pneumoniaeHospital-acquired
Proteus mirabilisUrolithiasis associated
PseudomonasCatheter-associated
EnterococcusNosocomial
Predisposing Factors:
  • Female sex (short urethra)
  • Sexual activity ("honeymoon cystitis")
  • Urinary obstruction (stones, BPH)
  • Catheterization
  • Diabetes mellitus
  • Pregnancy
  • Vesicoureteral reflux

Clinical Picture

Lower UTI (Cystitis):
  • Dysuria (burning/pain on urination)
  • Frequency and urgency of micturition
  • Suprapubic discomfort
  • Haematuria (blood in urine)
  • Cloudy, foul-smelling urine
  • No fever (or low-grade)
Upper UTI (Pyelonephritis):
  • All of the above PLUS:
  • High fever with chills and rigors
  • Loin/flank pain (costovertebral angle tenderness)
  • Nausea and vomiting
  • Systemic signs of infection

Investigations

  • Urine routine microscopy: Pyuria (>5 WBC/hpf), bacteriuria, RBCs
  • Urine culture and sensitivity (gold standard) - midstream clean catch
  • Blood tests: CBC (leukocytosis), blood culture if sepsis suspected
  • Ultrasound KUB: to rule out obstruction, abscess
  • IVP/CT urogram: recurrent UTIs

Management/Treatment

Uncomplicated Cystitis:
  • Trimethoprim-sulfamethoxazole (TMP-SMX) for 3 days
  • Nitrofurantoin for 5-7 days
  • Ciprofloxacin for 3 days
  • Increase fluid intake
Pyelonephritis (uncomplicated):
  • Oral fluoroquinolones (Ciprofloxacin) for 7-14 days
  • Hospitalization if severe: IV antibiotics (Ceftriaxone, Gentamicin)
  • IV fluids, antipyretics
Recurrent UTIs:
  • Low-dose prophylactic antibiotics
  • Post-coital prophylaxis
  • Treat underlying cause

πŸ“Œ TOPIC 2: HYPERTENSION

Definition

Hypertension = persistent elevation of blood pressure β‰₯ 140/90 mmHg on two separate occasions.
Classification (JNC 8 / ACC/AHA 2017):
StageSystolicDiastolic
Normal<120<80
Elevated120-129<80
Stage 1 HTN130-13980-89
Stage 2 HTNβ‰₯140β‰₯90
Hypertensive Crisis>180>120
Types:
  • Primary (Essential): 90-95% - no identifiable cause
  • Secondary: 5-10% - due to renal disease, endocrine causes, drugs

Clinical Features

Most patients are ASYMPTOMATIC (silent killer).
Symptoms when present:
  • Headache (occipital, worse in morning)
  • Dizziness and vertigo
  • Blurred vision
  • Epistaxis (nosebleed)
  • Palpitations
  • Shortness of breath
Signs:
  • Elevated BP on measurement
  • Retinal changes (hypertensive retinopathy): AV nicking, flame hemorrhages, papilledema in severe cases
  • Loud S2 (aortic component)
  • LV hypertrophy - apex displaced laterally

Complications (REMEMBER: "REACH-H")

1. Renal:
  • Hypertensive nephrosclerosis
  • Chronic kidney disease (CKD)
  • Proteinuria, haematuria
2. Eyes (Retinal):
  • Hypertensive retinopathy grades I-IV
  • Grade IV: papilledema (malignant hypertension)
  • Retinal vein occlusion
3. Arteries/Cardiovascular:
  • Coronary artery disease (angina, MI)
  • Left ventricular hypertrophy
  • Heart failure
  • Aortic dissection and aneurysm
4. Cerebrovascular:
  • Stroke (ischaemic or haemorrhagic) - most deadly complication
  • Transient ischaemic attacks (TIA)
  • Hypertensive encephalopathy
5. Heart:
  • Left ventricular hypertrophy (LVH)
  • Cardiac failure (initially diastolic, then systolic)
  • Atrial fibrillation

Management

Non-Pharmacological (Lifestyle):
  • DASH diet (low salt, <2.3g/day)
  • Weight reduction
  • Regular aerobic exercise
  • Reduce alcohol
  • Stop smoking
  • Stress management
Pharmacological (First-line drugs):
  • ACE inhibitors (Enalapril, Lisinopril): especially in diabetics, CKD
  • ARBs (Losartan, Valsartan): if ACE inhibitor intolerant
  • Calcium channel blockers (Amlodipine): elderly, isolated systolic HTN
  • Thiazide diuretics (Hydrochlorothiazide): first-line in many patients
  • Beta-blockers (Atenolol): with CAD, heart failure, tachycardia

πŸ“Œ TOPIC 3: DIABETES MELLITUS

Definition

A group of metabolic diseases characterized by chronic hyperglycaemia resulting from defects in insulin secretion, insulin action, or both.

Diagnostic Criteria

  • Fasting plasma glucose β‰₯ 126 mg/dL
  • 2-hour glucose β‰₯ 200 mg/dL (OGTT)
  • Random glucose β‰₯ 200 mg/dL + symptoms
  • HbA1c β‰₯ 6.5%

Type I vs Type II Diabetes - Key Differences

FeatureType I DMType II DM
Age of onsetUsually < 30 yearsUsually > 40 years (but rising in youth)
Body weightThin/normalObese (80-90%)
OnsetSudden/acuteGradual/insidious
PathologyAutoimmune destruction of beta cellsInsulin resistance + relative insulin deficiency
Insulin levelsVery low/absentNormal or elevated (early), low (late)
C-peptideAbsentPresent
AutoantibodiesPresent (anti-GAD, anti-islet cell)Absent
KetoacidosisCommon/prone (DKA)Rare (HONK/HHS)
Insulin neededAlways (life-dependent)Initially not required
Family historyLess strongStrong genetic predisposition
HLA associationHLA-DR3, DR4No specific HLA
TreatmentInsulin + dietDiet, oral drugs, Β± insulin

Complications of Type II Diabetes Mellitus

A. Acute Complications:
  1. Hyperosmolar Hyperglycaemic State (HHS/HONK): Very high blood sugar, severe dehydration, altered consciousness, NO significant ketosis
  2. Hypoglycaemia: Due to insulin/drug overdose - sweating, tremors, palpitations, confusion
B. Chronic (Long-term) Complications:
Microvascular (small vessel):
  1. Diabetic Nephropathy: Proteinuria β†’ nephrotic syndrome β†’ CKD β†’ end-stage renal disease
  2. Diabetic Retinopathy: Background β†’ proliferative β†’ blindness (leading cause of blindness in working-age adults)
  3. Diabetic Neuropathy: Peripheral (glove & stocking sensory loss), autonomic (postural hypotension, gastroparesis, impotence), mononeuropathy
Macrovascular (large vessel): 4. Coronary Artery Disease: MI (often silent) 5. Cerebrovascular disease: Stroke 6. Peripheral vascular disease: Poor circulation to limbs β†’ diabetic foot
Other: 7. Diabetic Foot: Combination of neuropathy + ischemia + infection β†’ ulcers, gangrene, amputation 8. Infections: Increased susceptibility to TB, UTI, skin infections, Candida 9. Cataracts and glaucoma

πŸ“Œ TOPIC 4: DIABETIC FOOT

Definition

A spectrum of conditions occurring in diabetic patients involving the foot, resulting from peripheral neuropathy, peripheral vascular disease, and secondary infection.

Pathophysiology (Triad)

  1. Peripheral neuropathy β†’ loss of sensation β†’ unnoticed injury
  2. Peripheral vascular disease (ischaemia) β†’ poor healing
  3. Infection β†’ rapid spread due to impaired immunity

Clinical Features

  • Painless ulcers (typically plantar, pressure points)
  • Charcot's neuropathic joint (deformed, Rocker-bottom foot)
  • Cold, pulseless foot (ischaemia)
  • Gangrene (dry or wet)
  • Cellulitis, abscess
  • Discoloration, callus formation
  • Wagner's Classification: Grade 0 (intact skin at risk) to Grade 5 (extensive gangrene)

Management

  • Strict glycaemic control (HbA1c < 7%)
  • Wound debridement
  • Antibiotics (broad spectrum - aerobic + anaerobic coverage)
  • Offloading pressure (total contact cast, special footwear)
  • Vascular surgery / revascularization if ischemic
  • Amputation as last resort
  • Patient education: Daily foot inspection, proper footwear

πŸ“Œ TOPIC 5: ANAEMIA & IRON DEFICIENCY ANAEMIA

Definition

Anaemia = reduction of haemoglobin below normal values.
  • Males: Hb < 13 g/dL
  • Females: Hb < 12 g/dL
  • Children: Hb < 11 g/dL (WHO)

Classification of Anaemia

A. Morphological (Based on RBC size & Hb content):
TypeMCVMCHCauses
Microcytic hypochromicLowLowIron deficiency, Thalassaemia, Sideroblastic
Normocytic normochromicNormalNormalAcute blood loss, Aplastic, CKD, Haemolytic
MacrocyticHighNormal/HighB12/Folate deficiency, Liver disease, Hypothyroidism
B. Pathophysiological:
  1. Blood loss (acute/chronic)
  2. Decreased production (nutritional, aplastic, bone marrow suppression)
  3. Increased destruction (haemolytic anaemia)

Iron Deficiency Anaemia (IDA)

Most common anaemia worldwide.
Causes:
  • Increased demand: Pregnancy, infancy, adolescence
  • Decreased intake: Poor diet (vegetarians, poverty)
  • Decreased absorption: Coeliac disease, gastrectomy, antacids
  • Chronic blood loss: Menorrhagia (most common in women), GI bleed (peptic ulcer, colorectal cancer), hookworm infestation

Clinical Features

General features of anaemia:
  • Pallor (conjunctival, palmar, nail bed)
  • Fatigue, weakness, easy fatigability
  • Breathlessness on exertion
  • Palpitations and tachycardia
  • Headache, difficulty concentrating
  • Pedal oedema in severe cases
Specific to Iron Deficiency:
  • Koilonychia (spoon-shaped nails)
  • Angular stomatitis (cracking at corners of mouth)
  • Glossitis (smooth, sore tongue)
  • Dysphagia (in Plummer-Vinson syndrome)
  • Pica (craving for chalk, mud, ice)
  • Blue sclerae

Investigations

  • CBC: Low Hb, Low MCV, Low MCH, Low MCHC
  • Peripheral smear: Microcytic, hypochromic RBCs, target cells, pencil cells
  • Serum ferritin: Low (best marker of iron stores)
  • Serum iron: Low
  • TIBC (Total Iron Binding Capacity): High
  • Transferrin saturation: Low (<16%)
  • Reticulocyte count: Normal or slightly raised

Management

  1. Treat the underlying cause (e.g., treat menorrhagia, hookworm)
  2. Oral iron: Ferrous sulphate 200mg TDS (3 times daily) for 3-6 months
    • Take on empty stomach with Vitamin C (for absorption)
    • Side effects: constipation, black stools, nausea
  3. Parenteral iron: IV/IM when oral not tolerated or absorption impaired
  4. Blood transfusion: Only if severe or cardiac compromise
  5. Dietary advice: Red meat, green leafy vegetables, legumes, fortified foods
  6. Response: Reticulocytosis in 5-10 days; Hb rises ~1g/dL/week

πŸ“Œ TOPIC 6: COMMUNICABLE DISEASES - MODES OF TRANSFER

Definition

A communicable disease is one that can be transmitted from one host to another (person to person, animal to person, or environment to person) either directly or indirectly.

Modes of Transmission

1. DIRECT TRANSMISSION Direct contact between source and susceptible host.
(a) Direct Contact:
  • Skin-to-skin: Scabies, ringworm, impetigo
  • Sexual contact: HIV/AIDS, gonorrhoea, syphilis, Hepatitis B
  • Droplet infection (large droplets, <1m): Influenza, common cold, mumps, meningococcal meningitis
(b) Vertical (Transplacental):
  • Mother to fetus: Rubella, CMV, HIV, Syphilis (TORCH infections)

2. INDIRECT TRANSMISSION
(a) Vehicle-borne (Contaminated objects):
  • Fomites (contaminated inanimate objects): Smallpox, diphtheria, trachoma
  • Water: Cholera, typhoid, hepatitis A, dysentery
  • Food: Salmonella, staphylococcal food poisoning, E. coli
  • Blood/blood products: HIV, Hepatitis B and C
  • Soil: Tetanus, hookworm, anthrax
(b) Vector-borne:
  • Biological vectors (pathogen multiplies in vector):
    • Mosquito (Anopheles): Malaria
    • Mosquito (Aedes): Dengue, yellow fever, chikungunya
    • Mosquito (Culex): Filariasis, Japanese encephalitis
    • Sandfly: Kala-azar (Leishmaniasis)
    • Tsetse fly: African sleeping sickness
    • Louse: Typhus
  • Mechanical vectors (no multiplication): Housefly carrying typhoid/cholera
(c) Airborne (droplet nuclei/<5 microns, travels >1m):
  • Pulmonary tuberculosis
  • Measles
  • Chickenpox
  • COVID-19
(d) Soil-borne:
  • Tetanus (Clostridium tetani spores)
  • Hookworm (larvae penetrate skin)
  • Anthrax

πŸ“Œ TOPIC 7: SCHIZOPHRENIA - SALIENT FEATURES

Definition

Schizophrenia is a chronic severe mental disorder characterized by disturbances in thinking, perception, emotion, and behavior. Onset typically 15-35 years.

Salient (Key) Features - Schneider's First Rank Symptoms

POSITIVE SYMPTOMS (excess/distortion of normal function):
  1. Hallucinations: Perceptions without external stimuli
    • Auditory (most common in schizophrenia): hearing voices commenting, arguing
    • Visual, olfactory, tactile less common
  2. Delusions: Fixed false beliefs not amenable to reason
    • Persecutory (paranoid): being followed, poisoned
    • Grandiose: believing one has special powers
    • Reference: events refer to self
    • Thought insertion/withdrawal/broadcasting
  3. Disorganized Thinking (Formal Thought Disorder):
    • Loose associations (derailment)
    • Tangential thinking
    • Word salad (incoherence)
  4. Disorganized or Catatonic Behavior:
    • Unpredictable agitation
    • Catatonic posturing (waxy flexibility)
    • Catatonic stupor
NEGATIVE SYMPTOMS (diminution of normal function) - "5 A's":
  1. Affective flattening - diminished emotional expression
  2. Alogia - poverty of speech
  3. Avolition - lack of motivation
  4. Anhedonia - inability to feel pleasure
  5. Asociality - social withdrawal
COGNITIVE SYMPTOMS:
  • Poor working memory, attention deficits
  • Poor executive function

Diagnosis (DSM-5 Criteria)

β‰₯ 2 of the following for β‰₯1 month:
  • Delusions, hallucinations, disorganized speech, disorganized behavior, negative symptoms
  • At least 1 must be delusions, hallucinations, or disorganized speech
  • Social/occupational dysfunction for β‰₯6 months

Management

  • Antipsychotics (first-line):
    • Typical (older): Haloperidol, Chlorpromazine
    • Atypical (newer, fewer side effects): Risperidone, Olanzapine, Clozapine
  • Psychosocial:
    • Cognitive Behavioral Therapy (CBT)
    • Family therapy
    • Social skills training
    • Occupational rehabilitation

πŸ“Œ TOPIC 8: HYPOTHYROIDISM - CLINICAL FEATURES

Definition

Hypothyroidism = deficiency of thyroid hormones (T3 and T4), leading to slowing of metabolic processes.

Causes

  • Primary: Hashimoto's thyroiditis (most common, autoimmune), iodine deficiency, radioiodine treatment, thyroidectomy
  • Secondary: Pituitary failure (low TSH)
  • Tertiary: Hypothalamic failure

Clinical Features (Remember: EVERYTHING SLOWS DOWN)

General/Constitutional:
  • Fatigue, lethargy, excessive sleepiness
  • Weight gain despite poor appetite
  • Cold intolerance
  • Constipation
  • Dry, coarse, rough skin
  • Hair loss (coarse, brittle hair), loss of outer 1/3 of eyebrow (Hertoghe sign)
Face and Neck:
  • Puffy face (periorbital puffiness/oedema)
  • Macroglossia (enlarged tongue)
  • Hoarse voice (myxoedematous infiltration of larynx)
  • Goitre (enlarged thyroid gland)
  • Dull, expressionless facies
Cardiovascular:
  • Bradycardia
  • Hypertension (diastolic)
  • Pericardial effusion
  • Cardiomegaly
Neurological/Psychological:
  • Slowed speech, slow thinking
  • Depression
  • Psychosis (rare - "myxoedema madness")
  • Delayed relaxation of deep tendon reflexes (hallmark sign)
  • Carpal tunnel syndrome
  • Cerebellar ataxia (rare)
Musculoskeletal:
  • Proximal myopathy (muscle weakness)
  • Myalgia, muscle cramps
  • Arthralgia
Reproductive:
  • Menorrhagia (heavy periods)
  • Infertility
Investigations:
  • TSH: High (primary hypothyroidism) - most sensitive test
  • Free T4: Low
  • Thyroid peroxidase antibodies (TPO-Ab): Positive in Hashimoto's
  • Lipid profile: High cholesterol, high LDL
Treatment: Levothyroxine (T4) replacement, starting low, titrating up

πŸ“Œ TOPIC 9: HYPERTHYROIDISM - CLINICAL FEATURES

Definition

Excess thyroid hormone production leading to hypermetabolic state.

Causes

  • Graves' disease (most common, autoimmune - TSH receptor antibodies)
  • Toxic multinodular goitre
  • Toxic adenoma
  • Excessive thyroxine intake

Clinical Features (EVERYTHING SPEEDS UP)

General:
  • Weight loss despite increased appetite
  • Heat intolerance, excessive sweating
  • Tremors (fine tremor of hands)
Cardiovascular:
  • Tachycardia, palpitations
  • Atrial fibrillation
  • Wide pulse pressure
  • Cardiac failure (high-output)
Neurological:
  • Anxiety, irritability, emotional lability
  • Insomnia
  • Hyperreflexia
GI:
  • Increased appetite
  • Diarrhoea
Eyes (Graves' disease):
  • Exophthalmos (proptosis) - eyes pushed forward
  • Lid lag, lid retraction
  • Ophthalmoplegia
Musculoskeletal:
  • Proximal myopathy
Menstrual:
  • Oligomenorrhoea (scanty/infrequent periods)
Investigations: TSH: Low; Free T3/T4: High; Radioiodine uptake scan
Treatment: Antithyroid drugs (Carbimazole, Propylthiouracil), Radioiodine therapy, Surgery (thyroidectomy), Beta-blockers (symptom control)

πŸ“Œ TOPIC 10: CIRRHOSIS

Definition

Cirrhosis is the end-stage of chronic liver disease characterized by replacement of normal liver parenchyma with fibrotic scar tissue and regenerative nodules, leading to disruption of liver architecture and function.

Causes

  • Chronic alcohol abuse (most common in western countries)
  • Viral hepatitis B and C (most common worldwide)
  • Non-alcoholic fatty liver disease (NAFLD/NASH)
  • Autoimmune hepatitis
  • Primary biliary cirrhosis/cholangitis
  • Wilson's disease, Haemochromatosis (metabolic)
  • Drugs (Methotrexate, Amiodarone)

Clinical Features

Compensated Cirrhosis (liver still functioning):
  • Often asymptomatic
  • Mild fatigue, anorexia
  • Spider naevi (spider angiomata) - on upper body
  • Palmar erythema
  • Hepatosplenomegaly
  • Parotid enlargement (in alcoholics)
  • Clubbing, leukonychia (white nails)
Decompensated Cirrhosis (liver failing):
  1. Jaundice: Yellow discoloration of sclera, skin, urine
  2. Ascites: Fluid in abdomen (portal hypertension + low albumin)
  3. Oedema: Peripheral pitting oedema
  4. Hepatic Encephalopathy: Confusion, altered consciousness, asterixis (flapping tremor), coma
  5. Variceal Haemorrhage: Bleeding from oesophageal/gastric varices β†’ haematemesis (bloody vomit), melaena
  6. Spontaneous Bacterial Peritonitis (SBP): Infection of ascitic fluid
  7. Hepatorenal Syndrome: Renal failure in advanced cirrhosis
  8. Coagulopathy: Bruising, bleeding tendency (low clotting factors)
Features of Portal Hypertension:
  • Splenomegaly
  • Oesophageal varices
  • Caput medusae (distended veins around umbilicus)
  • Rectal varices
Investigations: LFTs, Coagulation profile, Ultrasound abdomen, Liver biopsy (gold standard)
Management:
  • Treat underlying cause (stop alcohol, antiviral for hepatitis)
  • Ascites: Salt restriction, diuretics (spironolactone + furosemide), therapeutic paracentesis
  • Encephalopathy: Lactulose, Rifaximin, protein restriction
  • Varices: Propranolol (prophylaxis), endoscopic band ligation, TIPS
  • Liver transplant (definitive)

πŸ“Œ TOPIC 11: HEPATITIS B

Definition

Hepatitis B is a viral infection caused by Hepatitis B Virus (HBV - a DNA virus) that primarily affects the liver.

Transmission

  • Sexual contact (most common in developed countries)
  • Parenteral route: Blood transfusion, IV drug use, contaminated needles
  • Vertical: Mother to child (perinatal - most important in endemic areas like India)
  • Healthcare workers: Needlestick injuries
  • NOT transmitted by casual contact, food, water

Incubation Period

45-180 days (average 60-90 days)

Clinical Features

Acute Hepatitis B:
  • Pre-icteric phase: Fatigue, malaise, anorexia, nausea, vomiting, fever, arthralgia, right upper quadrant pain (1-2 weeks)
  • Icteric phase: Jaundice (yellow eyes/skin), dark urine (tea-colored), pale stools, hepatomegaly, tender liver, splenomegaly
  • Post-icteric phase: Gradual recovery over weeks
Outcomes:
  • 95% adults: Full recovery β†’ immunity
  • 5% adults β†’ Chronic Hepatitis B
  • 90% neonates β†’ Chronic HBV (high vertical transmission)
Chronic Hepatitis B β†’ Cirrhosis β†’ Hepatocellular Carcinoma (HCC)

Serology Markers

  • HBsAg: Marker of infection (positive in acute + chronic)
  • Anti-HBs: Marker of immunity (vaccination or recovery)
  • HBeAg: Marker of high infectivity/replication
  • Anti-HBe: Seroconversion (decreasing infectivity)
  • Anti-HBc IgM: Acute infection (window period)
  • HBV DNA: Viral load (most sensitive for active replication)

Management

  • Acute: Supportive (rest, fluids, nutrition)
  • Chronic: Antiviral therapy - Tenofovir (TDF), Entecavir (first-line)
  • Prevention: HBV Vaccine (most important - 3 doses: 0, 1, 6 months)
  • Post-exposure prophylaxis: Hepatitis B Immunoglobulin (HBIG) + vaccine

πŸ“Œ TOPIC 12: HEPATITIS C

Risk Factors

  • IV drug use (most common route in developed countries)
  • Blood transfusion (pre-screening era)
  • Healthcare worker needlestick injuries
  • Sexual transmission (less efficient than HBV)
  • Vertical transmission (less common than HBV)
  • Tattoos, body piercing with contaminated equipment

Clinical Features

  • Most (80%) are asymptomatic in acute phase
  • Acute: Mild jaundice, fatigue, nausea (if symptomatic)
  • 80% of HCV infections become chronic (vs 5% for HBV)
  • Chronic HCV: Slowly progressive liver damage over 20-30 years
  • β†’ Cirrhosis β†’ Hepatocellular carcinoma
Extra-hepatic manifestations:
  • Cryoglobulinaemia (vasculitis, purpura)
  • Membranoproliferative glomerulonephritis
  • SjΓΆgren-like syndrome
Complications: Cirrhosis (20-30%), Hepatocellular carcinoma, liver failure

Treatment

  • Direct Acting Antivirals (DAAs): Sofosbuvir + Ledipasvir/Daclatasvir/Velpatasvir
  • Cure rate >95%, oral treatment for 8-12 weeks
  • No vaccine available for HCV

πŸ“Œ TOPIC 13: CORONARY ARTERY DISEASE (CAD) & MYOCARDIAL INFARCTION

Definition

CAD = Atherosclerosis of coronary arteries causing narrowing of the lumen, leading to inadequate blood supply to myocardium (ischaemia or infarction).

Risk Factors

Non-modifiable:
  • Age (men >45, women >55)
  • Male sex
  • Family history of premature CAD
  • Genetics
Modifiable:
  • Dyslipidaemia: High LDL, low HDL, high triglycerides
  • Hypertension (most common risk factor in India)
  • Diabetes mellitus
  • Cigarette smoking
  • Obesity (BMI >30)
  • Physical inactivity
  • Metabolic syndrome
  • Stress (Type A personality)

Clinical Features of CAD

Stable Angina:
  • Central chest pain/pressure on exertion
  • Radiates to left arm, jaw, back
  • Relieved by rest or GTN (nitroglycerine) in <5 minutes
  • Precipitated by exercise, cold, stress, meals
Acute Coronary Syndromes (ACS):
  1. Unstable Angina: Pain at rest or increasing pattern, no enzyme rise
  2. NSTEMI: Partial blockage, elevated troponin, no ST elevation
  3. STEMI (Myocardial Infarction): Complete coronary artery occlusion

Features of Myocardial Infarction (STEMI)

Symptoms:
  • Severe crushing/squeezing central chest pain - worse than angina
  • Radiation to left arm, jaw, back
  • NOT relieved by GTN
  • Sweating (diaphoresis), cold and clammy skin
  • Nausea, vomiting
  • Dyspnoea
  • Feeling of impending doom
  • In diabetics/elderly: Silent MI (no pain)
Signs:
  • Tachycardia (or bradycardia if inferior MI)
  • Hypotension (cardiogenic shock in severe cases)
  • Signs of heart failure
Investigations:
  • ECG: ST elevation, pathological Q waves, T wave inversion
  • Troponin I/T: Rises in 3-6 hours, peaks 24-48h (most specific marker)
  • CK-MB: Rises in 3-6h, normalises in 48-72h
  • ECHO: Wall motion abnormality

Management of MI

  • MONA (immediate): Morphine, Oxygen, Nitrates, Aspirin
  • Dual antiplatelet: Aspirin + Clopidogrel/Ticagrelor
  • Anticoagulants: Heparin
  • Reperfusion (most important):
    • Primary PCI (percutaneous coronary intervention): within 90 minutes (preferred)
    • Thrombolysis (streptokinase, tPA): if PCI not available within 2 hours
  • Long-term: Statins, ACE inhibitors, Beta-blockers, aspirin

πŸ“Œ TOPIC 14: TUBERCULOSIS (TB)

Organs Affected by Tuberculosis

TB is a systemic disease. Can affect virtually any organ:
  1. Lungs (most common - 85%) - Pulmonary TB
  2. Lymph nodes (TB lymphadenitis) - most common extrapulmonary
  3. Pleura (pleural effusion)
  4. Bones and joints (Pott's disease - vertebral TB)
  5. Meninges (TB meningitis)
  6. Kidneys and genitourinary tract
  7. Bowel (intestinal TB)
  8. Liver, spleen (miliary TB)
  9. Pericardium
  10. Skin (lupus vulgaris)
  11. Adrenal glands
  12. Eyes (uveitis)

Pulmonary Tuberculosis - Clinical Features

Caused by Mycobacterium tuberculosis (acid-fast bacillus)
Symptoms:
  • Chronic cough (>3 weeks) - initially dry, then productive
  • Haemoptysis (blood in sputum) - important feature
  • Fever - low-grade, especially evening rise
  • Night sweats - drenching night sweats
  • Weight loss and anorexia - significant weight loss
  • Fatigue and weakness
  • Chest pain (pleuritic)
  • Breathlessness (in extensive disease)
Signs:
  • Cachexia (muscle wasting)
  • Pallor
  • Clubbing (chronic)
  • Dullness to percussion (consolidation/effusion)
  • Bronchial breathing, crepitations
  • Cervical lymphadenopathy

Diagnosis

  • Sputum AFB smear (Ziehl-Neelsen stain): Simple, quick - direct smear for acid-fast bacilli
  • Sputum culture: Gold standard (but slow - 4-8 weeks on Lowenstein-Jensen medium)
  • GeneXpert MTB/RIF: Rapid molecular test, also detects rifampicin resistance
  • Chest X-ray: Upper lobe infiltrates, cavitation, calcification, hilar adenopathy
  • Tuberculin skin test (Mantoux): Induration β‰₯10mm = positive
  • IGRA (Interferon Gamma Release Assay): QuantiFERON test

Management (RIPE)

  • First-line drugs: Rifampicin (R), Isoniazid (H/I), Pyrazinamide (Z/P), Ethambutol (E)
  • Intensive phase: 2 months of RHZE
  • Continuation phase: 4 months of RH
  • Total duration: 6 months (non-severe); 9-12 months for severe/extrapulmonary

πŸ“Œ TOPIC 15: HIV/AIDS

Modes of Spread of HIV

Caused by Human Immunodeficiency Virus (HIV - retrovirus), attacking CD4+ T-lymphocytes.
Three main routes:
  1. Sexual transmission (most common worldwide)
    • Unprotected sexual intercourse (anal > vaginal > oral)
    • Homosexual/heterosexual
  2. Parenteral (Blood-borne)
    • IV drug users sharing needles
    • Blood and blood product transfusion
    • Organ transplantation
    • Needlestick injuries (healthcare workers)
  3. Vertical (Mother to Child)
    • During pregnancy (transplacental)
    • During delivery (intrapartum - most common)
    • Breastfeeding (postnatal)
HIV is NOT transmitted by:
  • Casual contact, hugging, sharing utensils
  • Mosquitoes or other insects
  • Coughing, sneezing
  • Toilet seats, swimming pools

Clinical Features of AIDS

WHO Staging:
Stage 1 (Asymptomatic):
  • Asymptomatic
  • Persistent generalized lymphadenopathy (PGL)
  • CD4 >500 cells/mmΒ³
Stage 2 (Mild):
  • Minor weight loss (<10%)
  • Recurrent URTI
  • Herpes zoster
  • Angular cheilitis
  • Oral ulcers
Stage 3 (Advanced):
  • Weight loss >10%
  • Chronic diarrhoea >1 month
  • Oral candidiasis
  • Pulmonary TB
  • CD4 200-350 cells/mmΒ³
Stage 4 (AIDS-defining Illnesses):
  • Opportunistic infections:
    • PCP (Pneumocystis jirovecii pneumonia) - most common AIDS-defining illness
    • CMV retinitis β†’ blindness
    • Cryptococcal meningitis
    • Toxoplasmosis (brain abscess)
    • Disseminated Mycobacterium avium complex (MAC)
    • Esophageal candidiasis
  • HIV wasting syndrome: >10% weight loss
  • AIDS-defining malignancies:
    • Kaposi's sarcoma (skin purple lesions)
    • Non-Hodgkin's lymphoma
    • Cervical cancer
  • CD4 <200 cells/mmΒ³

Management

  • Antiretroviral Therapy (ART): Lifelong, started regardless of CD4 count
  • First-line regimen (India): Tenofovir + Lamivudine + Efavirenz (TLE)
  • Prophylaxis: Co-trimoxazole (for PCP when CD4 <200)
  • Prevention: Safe sex (condoms), clean needles, blood screening, PMTCT (Prevention of Mother to Child Transmission)
  • No cure; treatment controls viral replication

πŸ“Œ TOPIC 16: SWINE FLU (H1N1 Influenza)

Definition

Swine flu is an infection caused by the influenza A (H1N1) virus, which originated in pigs and crossed to humans, causing a pandemic in 2009.

Spread (Transmission)

  • Droplet transmission: Coughing, sneezing (main route)
  • Direct contact: Touching contaminated surfaces then touching face
  • NOT from eating cooked pork
  • Spreads person to person
  • Incubation period: 1-7 days (average 3 days)

Clinical Features

  • Fever (>38Β°C) - sudden onset
  • Cough (often dry)
  • Sore throat
  • Runny or stuffy nose
  • Body aches and myalgia
  • Headache
  • Chills
  • Fatigue
  • Diarrhoea and vomiting (more common than seasonal flu)
Warning Signs (severe illness):
  • Dyspnoea/breathlessness
  • Bluish skin (cyanosis)
  • Persistent vomiting, dehydration
  • Confusion/altered mental status
  • Chest pain
High-risk groups (Category C - need antiviral treatment):
  • Elderly, young children, pregnant women
  • Chronic diseases (diabetes, heart disease, lung disease)
  • Immunocompromised patients

Prevention

  • Oseltamivir (Tamiflu) vaccine - annual vaccination recommended
  • Hand hygiene (frequent washing with soap)
  • Covering mouth/nose when coughing/sneezing
  • Avoiding crowded places during outbreaks
  • Wearing masks (N95)
  • Isolation of suspected cases

Treatment

  • Oseltamivir (Tamiflu): 75mg twice daily for 5 days (antiviral)
  • Zanamivir (inhaled) as alternative
  • Supportive: rest, fluids, antipyretics, analgesics
  • Hospitalization for severe cases

πŸ“Œ TOPIC 17: COPD (Chronic Obstructive Pulmonary Disease)

Definition

COPD is a chronic, progressive respiratory disease characterized by persistent airflow limitation that is not fully reversible, associated with an abnormal inflammatory response to noxious particles or gases.

Causes

  • Cigarette smoking (most important cause - 90%)
  • Air pollution (outdoor and indoor - biomass fuel)
  • Occupational dust and chemicals
  • Alpha-1 antitrypsin deficiency (genetic, rare)
  • Recurrent childhood respiratory infections

Types

  1. Chronic Bronchitis - "Blue Bloater": productive cough for β‰₯3 months/year for β‰₯2 consecutive years, cyanosis, oedema
  2. Emphysema - "Pink Puffer": destruction of alveolar walls, barrel chest, pursed-lip breathing, little cyanosis

Clinical Features

  • Chronic cough (productive)
  • Increased sputum production
  • Progressive breathlessness on exertion (main complaint)
  • Wheeze
  • Barrel chest (increased AP diameter)
  • Pursed-lip breathing
  • Use of accessory muscles of respiration
  • Reduced breath sounds
  • Cyanosis (blue lips, fingertips)
  • Finger clubbing
  • Cor pulmonale (right heart failure): raised JVP, ankle oedema, hepatomegaly

Management

Non-pharmacological:
  • Smoking cessation (most important intervention - slows progression)
  • Pulmonary rehabilitation
  • Oxygen therapy (long-term in severe hypoxaemia - >15 hours/day)
  • Vaccinations: Influenza, Pneumococcal
Pharmacological:
  • Bronchodilators (first-line):
    • Short-acting beta-2 agonist (SABA): Salbutamol
    • Long-acting beta-2 agonist (LABA): Salmeterol, Formoterol
    • Long-acting anticholinergic (LAMA): Tiotropium
  • Inhaled Corticosteroids (ICS): Fluticasone (added if frequent exacerbations)
  • Oral theophylline: Add-on therapy
  • Roflumilast: PDE-4 inhibitor for severe COPD
Acute Exacerbation:
  • Increased bronchodilators
  • Systemic corticosteroids (Prednisolone 30-40mg for 5-7 days)
  • Antibiotics if infection suspected
Preventive Measures for COPD:
  • Smoking cessation and prevention
  • Reducing indoor air pollution
  • Occupational health measures
  • Vaccinations
  • Early detection and treatment

πŸ“Œ TOPIC 18: BRONCHIAL ASTHMA

Definition

Asthma is a chronic inflammatory disease of the airways characterized by variable airflow obstruction, airway hyperresponsiveness, and underlying inflammation.

Precipitating Factors (Triggers)

  1. Allergens: Dust mites, pollen, mould, pet dander, cockroach
  2. Respiratory infections: Viral URI (most common trigger in children), bacterial
  3. Exercise (Exercise-induced asthma)
  4. Cold air
  5. Air pollutants: Tobacco smoke, traffic fumes, occupational chemicals
  6. Drugs: Aspirin/NSAIDs (Samter's triad), beta-blockers
  7. Emotional stress and anxiety
  8. GERD (gastroesophageal reflux)
  9. Occupational agents: Isocyanates, flour, latex
  10. Hormonal changes: Menstruation, pregnancy
  11. Food additives: Sulphites (in wine, dried fruit), tartrazine

Clinical Features

  • Episodic breathlessness (dyspnoea)
  • Wheeze (expiratory wheeze)
  • Chest tightness
  • Cough (especially nocturnal/early morning)
  • Symptoms worsen at night or in early morning
Signs:
  • Bilateral expiratory wheeze
  • Prolonged expiration
  • Use of accessory muscles
  • Tachypnoea

Management

  • Reliever: SABA (Salbutamol) - used as needed for acute symptoms
  • Controller/Preventer: Inhaled corticosteroids (ICS) - Beclomethasone
  • LABA + ICS combination for persistent asthma
  • Leukotriene receptor antagonists: Montelukast
  • Biologics for severe asthma: Omalizumab (anti-IgE)
  • Acute attack: Nebulised Salbutamol + Ipratropium, systemic steroids, O2, IV Magnesium if severe

πŸ“Œ TOPIC 19: SKIN CONDITIONS

A. Classification of Skin Lesions

Primary Lesions (arise on previously normal skin):
LesionDescriptionExample
MaculeFlat, colour change, <1cmFreckle, vitiligo, petechia
PatchFlat, colour change, >1cmCafΓ©-au-lait, melasma
PapuleRaised, solid, <1cmWart, lichen planus
PlaqueRaised, flat-topped, >1cmPsoriasis
NoduleRaised, solid, >1cm, deeperLipoma, melanoma
VesicleBlister <0.5cm, fluid-filledChickenpox, herpes simplex
BullaBlister >0.5cmPemphigus, bullous pemphigoid
PustulePus-filled raised lesionAcne, folliculitis
Wheal/UrticaRaised, erythematous, transientUrticaria
Secondary Lesions (develop from primary):
  • Scale, crust, erosion, ulcer, fissure, scar, atrophy, excoriation

B. Urticaria (Hives)

Definition: Urticaria is a skin disorder characterized by transient, itchy wheals (hives) - raised, erythematous, oedematous plaques with central pallor.
Causes:
  • Allergic (IgE-mediated - Type I hypersensitivity): drugs (penicillin, aspirin), foods (nuts, seafood, eggs), insect stings
  • Physical: cold urticaria, heat, pressure, dermographism (skin writing), exercise
  • Infections: viral, bacterial, parasitic
  • Autoimmune
  • Idiopathic (50% cases)
  • Chronic urticaria: >6 weeks duration
Clinical Features:
  • Intensely itchy wheals/hives
  • Multiple raised erythematous plaques with central pallor
  • Lesions come and go (transient - each lesion <24 hours)
  • No scarring
  • Can be accompanied by angioedema (deeper swelling of lips, tongue, throat - dangerous if airway involved)
  • Dermatographism: writing on skin produces wheal
Management:
  • Remove/avoid triggering cause (most important)
  • Antihistamines (first-line):
    • Non-sedating (2nd generation): Cetirizine, Loratadine (preferred)
    • Sedating (1st generation): Chlorphenamine (for acute/severe)
  • Corticosteroids (short course): for severe/resistant cases
  • Anaphylaxis with urticaria: Adrenaline (Epinephrine) 0.5mg IM - EMERGENCY
  • Anti-IgE (Omalizumab): for chronic refractory urticaria
  • Avoid aspirin, NSAIDs, alcohol (can worsen)

C. Acne Vulgaris

Definition: Chronic inflammatory disease of pilosebaceous units.
Pathogenesis:
  1. Increased sebum production (androgens)
  2. Follicular hyperkeratosis (plugging)
  3. Cutibacterium acnes (bacteria) proliferation
  4. Inflammation
Clinical Features:
  • Comedones (open = blackheads, closed = whiteheads)
  • Papules and pustules
  • Nodules and cysts (severe)
  • Scarring
  • Mainly face, chest, upper back
Management:
  • Mild: Topical retinoids, benzoyl peroxide, topical antibiotics (clindamycin)
  • Moderate: Oral antibiotics (doxycycline, minocycline) + topical
  • Severe (nodular/cystic): Oral isotretinoin (Accutane) - most effective
  • Hormonal (females): Combined OCP, spironolactone

D. Psoriasis

Definition: Chronic inflammatory skin disease with accelerated epidermal proliferation (turnover every 3-4 days vs normal 28-30 days).
Clinical Features:
  • Well-demarcated, erythematous plaques with silvery-white scales
  • Mainly on extensor surfaces (elbows, knees), scalp, lower back
  • Koebner's phenomenon (lesions appear at trauma sites)
  • Auspitz sign (pinpoint bleeding when scale removed)
  • Nail changes: pitting, onycholysis, subungual hyperkeratosis
  • Psoriatic arthritis (15-20% cases)
Management:
  • Topical: Corticosteroids, vitamin D analogues (calcipotriol), tar, retinoids
  • Phototherapy: Narrowband UVB, PUVA
  • Systemic (severe): Methotrexate, Cyclosporine, Acitretin
  • Biologics: Anti-TNF (Adalimumab, Infliximab), anti-IL-17 (Secukinumab)

E. Fungal Infections of Skin

Types:
  1. Tinea (Dermatophytosis):
    • Tinea capitis (scalp - ringworm of scalp)
    • Tinea corporis (body - ringworm)
    • Tinea cruris (groin - "jock itch")
    • Tinea pedis (foot - "athlete's foot")
    • Tinea unguium (nails = Onychomycosis)
    • Features: Circular, red, scaly ring-shaped lesion with central clearing
  2. Candidiasis:
    • Oral thrush (white plaques in mouth)
    • Vaginal candidiasis (curdy white discharge, itching)
    • Intertrigo (skin folds)
    • Risk factors: Diabetes, antibiotics, immunosuppression
  3. Pityriasis versicolor: Malassezia furfur; hypo/hyperpigmented patches, fine scaling on trunk
Management: Topical antifungals (Clotrimazole, Miconazole); Oral antifungals for resistant/extensive (Fluconazole, Itraconazole, Griseofulvin for tinea capitis)

πŸ“Œ TOPIC 20: UROLITHIASIS (KIDNEY STONES) & HEMATURIA

Hematuria - Definition

Hematuria = presence of blood in urine.
  • Gross/macroscopic: Visible to naked eye
  • Microscopic: >3 RBC/HPF on microscopy
Causes: UTI, urolithiasis, glomerulonephritis, tumours, TB of urinary tract, trauma, coagulation disorders

Urolithiasis - Clinical Features

Types of stones: Calcium oxalate (most common, 70%), Uric acid, Struvite (infection stones), Cystine
Clinical Features:
  • Renal colic: Severe, colicky (wave-like) pain - originates in loin, radiates to groin, inner thigh, labia/scrotum
  • Haematuria (blood in urine)
  • Nausea and vomiting
  • Restlessness (unable to find comfortable position)
  • Fever if infection superimposed (urosepsis)
  • Symptoms of obstruction: oliguria, anuria
Investigations:
  • Urinalysis: RBCs, WBCs if infection, pH
  • CT-KUB (non-contrast) - gold standard for stone diagnosis
  • Ultrasound abdomen (first-line, especially for renal stones)
  • X-ray KUB: radio-opaque stones (calcium, struvite)
  • IVU (Intravenous Urography)
  • Stone analysis
Management:
  • Conservative (stones <5mm usually pass spontaneously):
    • High fluid intake (>2-3L/day)
    • Analgesia (NSAIDs, opioids for colic)
    • Alpha-blockers (Tamsulosin) for ureteric stones
  • Interventional:
    • Extracorporeal Shock Wave Lithotripsy (ESWL): non-invasive, for small-medium renal stones
    • Ureteroscopy (URS) + laser lithotripsy: ureteric stones
    • Percutaneous Nephrolithotomy (PCNL): large/complex renal stones (>2cm)
    • Open surgery: rarely needed

πŸ“Œ TOPIC 21: GERD (Gastroesophageal Reflux Disease)

Definition

GERD is a condition where stomach acid flows back into the oesophagus due to incompetence of the lower oesophageal sphincter (LOS), causing symptoms and/or mucosal damage.

Clinical Features

Typical symptoms:
  • Heartburn (pyrosis) - burning sensation in chest, behind sternum, worse after meals, lying down, bending
  • Regurgitation - sour/acid taste in mouth, fluid coming back up
  • Waterbrash - excess saliva due to esophageal acid irritation
Atypical symptoms:
  • Chronic cough (acid aspiration)
  • Hoarse voice (laryngopharyngeal reflux)
  • Asthma exacerbation
  • Dental erosions
  • Chest pain (non-cardiac)
Complications:
  • Oesophagitis
  • Oesophageal stricture (dysphagia)
  • Barrett's oesophagus (metaplasia - risk of adenocarcinoma)
Management:
  • Lifestyle: Weight loss, avoid precipitants (fatty food, coffee, alcohol, spicy food), elevate head of bed, small frequent meals, avoid lying down after meals
  • Proton Pump Inhibitors (PPIs): Omeprazole, Pantoprazole - first-line pharmacotherapy
  • H2-receptor antagonists: Ranitidine (second-line)
  • Antacids: Symptom relief
  • Surgery: Fundoplication (Nissen) for resistant cases

πŸ“Œ TOPIC 22: LUNG ABSCESS

Definition

Lung abscess is a localized area of necrosis and pus formation within the lung parenchyma, resulting in a cavitary lesion.

Causes

  • Aspiration (most common): Anaerobic organisms, in patients with impaired consciousness (alcoholics, seizures, post-anaesthesia)
  • Pneumonia (secondary lung abscess - Staphylococcus aureus, Klebsiella)
  • Septic emboli (IV drug users, endocarditis)
  • Obstruction (tumour, foreign body)
  • Amoebic abscess (right lower lobe, rupture from liver)
  • Immunocompromised (TB, Nocardia, fungi)

Clinical Features

  • Fever with chills and sweats
  • Putrid, foul-smelling sputum (in anaerobic infections - hallmark)
  • Productive cough with copious sputum
  • Haemoptysis
  • Chest pain (pleuritic)
  • Weight loss, malaise
  • Clubbing (if chronic)
  • On auscultation: bronchial breathing, amphoric breath sounds over cavity

Investigations

  • Chest X-ray: Cavity with air-fluid level (hallmark)
  • CT chest: More detail
  • Sputum culture
  • Bronchoscopy: if obstruction suspected or to obtain cultures

Management

  • Prolonged antibiotics (4-6 weeks minimum):
    • Anaerobic: Metronidazole + Penicillin or Amoxicillin-clavulanate
    • If Staphylococcus: Flucloxacillin or Vancomycin (MRSA)
  • Postural drainage and chest physiotherapy (IMPORTANT for physiotherapists!)
  • Surgical drainage or resection: if no response to medical treatment

πŸ“Œ TOPIC 23: LIVER ABSCESS

Types

  1. Pyogenic (Bacterial) Liver Abscess: E. coli, Klebsiella (usually multiple, right lobe)
  2. Amoebic Liver Abscess: Entamoeba histolytica (single, right lobe, "anchovy paste" pus)

Clinical Features

  • Fever with chills
  • Right upper quadrant pain
  • Tender hepatomegaly
  • Jaundice (mild)
  • Weight loss
  • Referred right shoulder tip pain (diaphragm irritation)

Management

  • Aspiration or drainage (ultrasound-guided)
  • Antibiotics: Metronidazole (for amoebic), broad-spectrum for pyogenic

πŸ“Œ TOPIC 24: PROTEIN DEFICIENCY DISEASES

A. Kwashiorkor (Protein Deficiency with adequate calories)

  • Age: Typically 1-3 years (weaned child)
  • Cause: Adequate carbohydrate but protein-deficient diet
Features:
  • Oedema (pitting, most characteristic) - due to hypoalbuminaemia
  • Growth retardation
  • Muscle wasting (hidden by oedema)
  • Moon face (puffy face)
  • Hepatomegaly (fatty liver)
  • Skin: Dermatosis - "flaky paint" depigmentation, "crazy-paving" appearance
  • Hair changes: Sparse, fine, depigmented, easily pluckable (Flag sign - alternating bands)
  • Apathetic, irritable, miserable child
  • Serum albumin: Very low

B. Marasmus (Protein-Energy Malnutrition)

  • Age: <1 year typically
  • Cause: Severe deficiency of both protein AND calories
Features:
  • Severe muscle wasting - "skin and bones" appearance
  • "Old man face" (senile facies)
  • Loss of subcutaneous fat - "baggy pants" skin folds
  • No oedema (distinguishes from kwashiorkor)
  • Severe weight loss (>60% expected weight)
  • Alert and hungry but weak
  • Hair and skin relatively normal

C. Marasmic Kwashiorkor

  • Combined features of both

Management

  • WHO 10-step protocol for severe malnutrition
  • F-75 formula (low protein, low energy initially) β†’ F-100 (catch-up growth)
  • Therapeutic Ready-to-Use Food (RUTF): Plumpynut
  • Micronutrient supplementation (zinc, Vitamin A, folate, iron)
  • Treat infections

πŸ“Œ TOPIC 25: OLIGURIA

Definition

Oliguria = urine output <400 mL/24 hours (or <0.5 mL/kg/hour). Anuria = urine output <100 mL/24 hours.

Causes (Pre-renal, Renal, Post-renal)

Pre-renal (decreased perfusion to kidneys - most common):
  • Hypovolaemia: dehydration, hemorrhage, burns
  • Reduced cardiac output: Heart failure, cardiogenic shock
  • Decreased vascular tone: Septicaemia, anaphylaxis, liver failure
Renal (intrinsic kidney disease):
  • Acute tubular necrosis (ATN) - most common intrinsic cause
  • Glomerulonephritis
  • Interstitial nephritis (drugs)
  • Vascular: Renal artery/vein thrombosis
Post-renal (obstruction of urinary outflow):
  • Bladder outlet obstruction: BPH, urethral stricture
  • Bilateral ureteric obstruction: Stones, tumour, retroperitoneal fibrosis
  • Blocked urinary catheter

Management

  • Identify and treat underlying cause
  • Fluid challenge (250-500ml NS) - for pre-renal
  • Catheterize (for post-renal/monitoring)
  • Dialysis if renal failure severe
  • Monitor urine output, creatinine, electrolytes

πŸ“Œ TOPIC 26: HOARSE VOICE - CAUSES AND MANAGEMENT

Definition

Hoarseness = any change in voice quality including roughness, breathiness, strain, or altered pitch.

Causes

Benign:
  • Acute laryngitis (most common) - viral/bacterial, excessive voice use
  • Chronic laryngitis - smoking, chronic irritants
  • Vocal cord nodules (singer's nodules, "screamer's nodules")
  • Vocal cord polyps
  • Vocal cord cysts
  • Functional dysphonia
Systemic diseases:
  • Hypothyroidism (myxoedema infiltration of vocal cords)
  • GERD (laryngopharyngeal reflux)
  • Reinke's oedema (smokers)
Neurological:
  • Recurrent laryngeal nerve (RLN) palsy:
    • Left RLN: Mediastinal lymphoma, lung cancer (Pancoast), aortic aneurysm
    • Right RLN: Thyroid surgery, subclavian vessel disease
  • Upper motor neurone lesions
Malignant (RED FLAG - hoarseness >3 weeks in smoker/elderly):
  • Laryngeal carcinoma (most important to exclude)
  • Thyroid carcinoma invading larynx
  • Metastatic lymph nodes compressing RLN
Trauma:
  • Intubation injury
  • Neck trauma

Management

  • History: Duration, progression, smoking, voice use, dysphagia, weight loss
  • Investigation: Laryngoscopy (direct or indirect - essential investigation)
  • Treat underlying cause
  • Voice rest for acute laryngitis
  • Speech therapy for vocal cord lesions/functional dysphonia
  • Surgery: Microlaryngoscopy for polyps, nodules, laryngeal cancer

πŸ“Œ TOPIC 27: ECT (Electroconvulsive Therapy)

Definition

ECT is a psychiatric treatment in which a brief electrical current is passed through the brain under general anaesthesia to induce a controlled seizure.

Indications (IMPORTANT)

  1. Severe depression with psychotic features or suicidal risk
  2. Severe depression not responding to antidepressants
  3. Bipolar disorder - severe manic or depressive episode
  4. Schizophrenia - catatonic type
  5. Post-partum psychosis
  6. Rapid response needed (suicidal, refusing food/water)

Contraindications

  • Recent MI or stroke
  • Raised intracranial pressure
  • Aortic aneurysm
  • Phaeochromocytoma

Procedure

  • Written informed consent
  • Pre-ECT: Fasting, ECG, blood tests
  • General anaesthesia + muscle relaxant (to prevent injury during seizure)
  • Electrode placement (bilateral/unilateral)
  • Brief electrical stimulus (0.5-2 seconds) induces grand mal seizure (30-90 seconds)
  • Monitoring: ECG, EEG, SpO2
  • Typically: 6-12 sessions (2-3 times/week)

Side Effects

  • Short-term: Confusion, headache, muscle aches
  • Memory loss (most common complaint): retrograde and anterograde amnesia (usually temporary)
  • Cardiovascular: Bradycardia, hypertension (transient)
  • Bone fractures (prevented by muscle relaxants)

πŸ“Œ TOPIC 28: HEART MALFORMATIONS (Congenital Heart Disease)

Classification

A. Acyanotic (Left-to-right shunt - no cyanosis initially):
  1. VSD (Ventricular Septal Defect) - most common CHD overall
    • Harsh pansystolic murmur at left sternal border
    • Can cause Eisenmenger's syndrome (reversal of shunt β†’ cyanosis)
  2. ASD (Atrial Septal Defect)
    • Ejection systolic murmur, fixed split S2
    • Often asymptomatic in childhood
  3. PDA (Patent Ductus Arteriosus)
    • Continuous "machinery" murmur
    • More common in premature infants, rubella
  4. Coarctation of Aorta
    • Hypertension in arms, weak pulses in legs
    • Rib notching on CXR
B. Cyanotic (Right-to-left shunt - cyanosis from birth/infancy):
  1. Tetralogy of Fallot (TOF) - most common cyanotic CHD
    • Four features: VSD + Right Ventricular Hypertrophy + Pulmonary Stenosis + Overriding Aorta
    • Tet spells (hypercyanotic spells), squatting relieves symptoms
    • Boot-shaped heart on CXR
  2. Transposition of Great Arteries (TGA)
    • Aorta from RV, pulmonary artery from LV
    • Cyanosis at birth
    • Egg-on-string CXR appearance
  3. Tricuspid Atresia

πŸ“Œ QUICK REFERENCE: IMPORTANT DRUG NAMES & TREATMENTS

ConditionFirst-line Treatment
UTI (simple)TMP-SMX or Nitrofurantoin or Ciprofloxacin
HypertensionACE inhibitor, ARB, CCB, Thiazide diuretic
Type 2 DMMetformin (first-line)
Type 1 DMInsulin
Iron Deficiency AnaemiaFerrous sulphate
HypothyroidismLevothyroxine (T4)
HyperthyroidismCarbimazole / PTU
AsthmaInhaled Salbutamol (reliever) + ICS (preventer)
COPDTiotropium (LAMA) / LABA
TBRHZE Γ— 2 months β†’ RH Γ— 4 months
HIVTDF + 3TC + EFV (Tenofovir+Lamivudine+Efavirenz)
Hepatitis CSofosbuvir-based DAA regimens
GERDOmeprazole/Pantoprazole (PPI)
UrticariaCetirizine (non-sedating antihistamine)
SchizophreniaRisperidone / Olanzapine (atypical antipsychotics)
CAD/MIAspirin + Clopidogrel + Statin + PCI
Swine FluOseltamivir (Tamiflu)
Acne (severe)Oral isotretinoin
ECT indicationsSevere refractory depression, catatonic schizophrenia

πŸ“ EXAM TIPS FOR PHYSIOTHERAPY STUDENTS

  1. Most repeated topics (prepare first): UTI, Diabetes (Type I vs II + complications), Hypertension complications, Iron deficiency anaemia, Communicable diseases, Schizophrenia, Hypothyroidism, TB
  2. For long questions (15 marks): Use proper headings - Definition β†’ Causes β†’ Clinical features β†’ Investigations β†’ Management. Each heading gets marks.
  3. Comparisons/tables: Always draw a comparison table for Type I vs Type II DM - examiners love it.
  4. Remember mode mnemonics:
    • Communicable disease: Direct, Indirect (Vehicle, Vector, Airborne, Soil)
    • TB management: RHZE (Rifampicin, Isoniazid, Pyrazinamide, Ethambutol)
    • Anaemia "5 A's" of IDA symptoms: Anaemia, Angular stomatitis, Atrophic glossitis, Achlorhydria, Alopecia
  5. Physiotherapy relevance: For conditions like COPD and lung abscess, mention chest physiotherapy (postural drainage, breathing exercises, vibration) as part of management - this shows your clinical thinking!
  6. Diagrams: Draw wherever possible - skin lesion classifications, TB X-ray (cavity with air-fluid level), ECG changes in MI.
Good luck with your exam! 🎯
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