CNS case sheet for medicine postings with detailed history taking

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I now have enough textbook context and background to compose a comprehensive CNS case sheet. Let me compile it from Bradley and Daroff's Neurology in Clinical Practice plus standard clinical medicine framework.

CNS Case Sheet — Medicine Postings

Central Nervous System: Detailed History Taking & Examination Proforma


SECTION 1 — PATIENT IDENTIFICATION

FieldDetails
Name
Age / Sex
IP/OP No.
Ward / Bed No.
Occupation
Address
Informant(Patient / Relative / Bystander) — Reliability:
Date of Admission
Date of Examination

SECTION 2 — CHIEF COMPLAINTS

(In patient's own words, in chronological order with duration)
  1. _____________ — since ___________
  2. _____________ — since ___________
  3. _____________ — since ___________

SECTION 3 — HISTORY OF PRESENTING ILLNESS

General Pointers

  • Mode of onset: Sudden / Acute / Sub-acute / Chronic / Insidious
  • Progression: Static / Progressive / Relapsing-remitting / Stepwise
  • Course: Improving / Worsening / Fluctuating

A. Headache (if present)

  • Site: Unilateral / Bilateral / Holocranial / Occipital / Frontal / Peri-orbital
  • Onset: Sudden ("thunderclap") / Gradual
  • Character: Throbbing / Pressing / Band-like / Stabbing / Boring
  • Severity: Mild / Moderate / Severe (VAS scale 1–10)
  • Duration: Seconds / Minutes / Hours / Days
  • Radiation: Neck / Face / Shoulder / Back
  • Time of occurrence: Early morning / Nocturnal / Continuous
  • Aggravating factors: Bending forward, coughing, straining, physical activity, light, noise
  • Relieving factors: Rest, analgesics, darkness, sleep
  • Associated features: Nausea/vomiting, photophobia, phonophobia, aura, visual changes, fever, neck stiffness
  • Prior history of similar headache: Yes / No

B. Seizures / Fits (if present)

  • Type of onset: Focal / Generalised / Unknown
  • Aura: Rising epigastric sensation / Visual / Auditory / Olfactory / Déjà vu / Fear (note: mesial temporal auras = rising epigastric sensation; occipital = elementary visual; lateral temporal = auditory)
  • Motor manifestations: Tonic / Clonic / Tonic-clonic / Myoclonic / Atonic
  • Lateralisation: Unilateral / Bilateral / Head/eye deviation (direction)
  • Automatisms: Lip smacking / Oro-alimentary / Hand automatisms / Bipedal / Verbal
  • Duration of episode
  • Loss of consciousness: Yes / No
  • Post-ictal state: Confusion / Headache / Todd's palsy / Sleepiness / Duration
  • Tongue bite / Urinary/faecal incontinence
  • Frequency: per day / week / month
  • Precipitants: Sleep deprivation / Alcohol / Fever / Stress / Menstruation / Flashing lights
  • Risk factors: Febrile seizures in infancy, meningitis/encephalitis (especially before age 5), head trauma, family history (Bradley & Daroff)

C. Loss of Consciousness / Altered Sensorium

  • Onset: Sudden / Gradual
  • Duration
  • Preceding symptoms: Prodrome, warning
  • Depth: GCS at time of event
  • Associated: Seizures, injuries, incontinence, cyanosis
  • Recovery: Complete / Partial / Time to recovery

D. Weakness / Paralysis

  • Distribution: Monoplegia / Hemiplegia / Paraplegia / Tetraplegia / Diplegia
  • Onset: Sudden (stroke) / Progressive (tumour, motor neurone disease) / Episodic
  • UMN vs LMN features in history: Stiffness and spasticity (UMN) vs floppiness and wasting (LMN)
  • Progression: Fixed / Ascending (Guillain-Barré) / Descending
  • Associated sensory loss: Yes / No / Level
  • Bladder and bowel involvement
  • Diurnal variation: Morning stiffness / End-of-day fatigue (myasthenia)

E. Sensory Symptoms

  • Type: Numbness / Tingling / Paraesthesia / Pain / Burning / Electric shocks
  • Distribution: Dermatomal / Peripheral nerve / "Stocking-glove" / Hemibody / Saddle area
  • Loss of specific modalities: Pain/temperature vs vibration/joint position sense
  • Lhermitte's sign (electric shock on neck flexion — demyelination)
  • Trophic changes, pressure sores

F. Visual Symptoms

  • Blurring: Monocular (anterior to chiasm) / Binocular
  • Diplopia: Horizontal / Vertical / Oblique; worse at distance vs near
  • Visual field defects: Hemianopia / Quadrantanopia / Tunnel vision / Central scotoma
  • Transient visual loss (amaurosis fugax)
  • Oscillopsia / Visual obscurations / Photopsia

G. Speech and Language

  • Dysarthria: Slurring / Nasal / Scanning / Explosive / Low volume
  • Dysphasia/Aphasia: Expressive (Broca's — non-fluent) / Receptive (Wernicke's — fluent) / Global
  • Dysphonia: Hoarseness
  • Dysphagia: Solids / Liquids / Both

H. Gait and Balance

  • Type: Wide-based (cerebellar/sensory ataxia) / Steppage / Scissor / Spastic / Festinant / High-stepping / Waddling
  • Falls: Frequency, direction (retropulsion in Parkinsonism)
  • Dizziness / Vertigo: True vertigo (rotational) vs light-headedness; positional

I. Involuntary Movements

  • Type: Tremor / Chorea / Athetosis / Ballismus / Myoclonus / Tics / Dystonia / Fasciculations
  • For tremor: Rest (Parkinsonism) / Action (Essential tremor) / Intention (cerebellar)
  • Relation to posture, activity, sleep

J. Cognitive and Behavioural Symptoms

  • Memory: Short-term / Long-term deterioration
  • Orientation: Time / Place / Person
  • Language deterioration
  • Personality change / Disinhibition / Apathy
  • Sleep disturbance: Insomnia / Hypersomnia / REM behaviour disorder
  • Hallucinations: Visual / Auditory / Tactile

K. Autonomic Symptoms

  • Bladder: Frequency / Urgency / Retention / Incontinence
  • Bowel: Constipation / Incontinence
  • Sweating: Hyperhidrosis / Anhidrosis
  • Postural dizziness (orthostatic hypotension)
  • Sexual dysfunction

SECTION 4 — PAST HISTORY

SystemDetails
Similar episodesYes / No
HypertensionYes / No; duration, drugs
Diabetes mellitusYes / No; duration, control
Cardiac diseaseIHD / AF / RHD / Prosthetic valves
Stroke / TIAYes / No; residual deficit
EpilepsyYes / No; onset age, drugs
Meningitis / EncephalitisYes / No; age at occurrence
Head injury / Spine injuryYes / No; nature
TuberculosisYes / No; treatment
HIV / ImmunosuppressionYes / No
Surgical proceduresYes / No
Blood transfusionsYes / No
Drug allergies

SECTION 5 — FAMILY HISTORY

  • Similar neurological illness in family members (epilepsy, migraine, muscular dystrophy, Huntington's, spinocerebellar ataxia)
  • Three-generation pedigree if hereditary condition suspected (Bradley & Daroff)
  • Consanguinity: Yes / No
  • Neurodegenerative disorders (Parkinson's, Alzheimer's, Friedreich's ataxia)
  • Sudden unexplained death

SECTION 6 — PERSONAL HISTORY

ItemDetails
DietVegetarian / Non-vegetarian / Nutritional deficiencies
AppetiteNormal / Decreased / Increased
SleepNormal / Disturbed
Bowel/BladderNormal / Altered
SmokingYes / No; pack-years
AlcoholYes / No; type, quantity, duration; withdrawal symptoms
Illicit drugsYes / No; type, route
OccupationExposure to toxins (lead, mercury, organophosphates)
Marital history
Travel historyEndemic areas (neurocysticercosis, malaria cerebral, rabies)

SECTION 7 — TREATMENT HISTORY

  • Current medications (especially antiepileptics, antihypertensives, anticoagulants, steroids, immunosuppressants)
  • Previous neurological treatments and response
  • Herbal / OTC medications

SECTION 8 — SOCIOECONOMIC & DEVELOPMENTAL HISTORY (Paediatric cases)

  • Birth: Full-term / Premature; birth weight; mode of delivery
  • Perinatal: Asphyxia, NICU stay, neonatal seizures
  • Developmental milestones: Head control / Sitting / Standing / Walking / First words / Sentences
  • School performance
  • Immunisation history
  • Regression of milestones: Yes / No

SECTION 9 — GENERAL PHYSICAL EXAMINATION

Vitals

ParameterValue
Pulse/min; rhythm; volume; character
Blood PressuremmHg (both arms; lying and standing)
Respiratory Rate/min
Temperature°F / °C
SpO₂%
GCSE__ V__ M__ = __ /15

General Examination

  • Built and nourishment: Good / Poor
  • Pallor / Icterus / Cyanosis / Clubbing / Lymphadenopathy / Oedema
  • Skin: Café-au-lait spots / Ash-leaf macules / Shagreen patches / Port wine stain / Neurofibromas (neurocutaneous markers)
  • Head circumference (paediatric): Microcephaly / Macrocephaly
  • Spine: Kyphosis / Scoliosis / Hairy patch / Spina bifida / Sacral dimple
  • Neck stiffness: Kernig's sign / Brudzinski's sign (meningeal irritation)

SECTION 10 — SYSTEMIC EXAMINATION

Cardiovascular: (embolic sources)

  • Murmurs, AF, peripheral pulses, carotid bruits

Respiratory:

  • Consolidation, effusion (TB, paraneoplastic)

Abdomen:

  • Hepatosplenomegaly (storage disorders, Wilson's disease)
  • Liver: cirrhosis (hepatic encephalopathy)

SECTION 11 — NEUROLOGICAL EXAMINATION

A. HIGHER MENTAL FUNCTIONS (Cortical Functions)

1. Consciousness

  • GCS: Eyes (1–4) / Verbal (1–5) / Motor (1–6)
  • AVPU: Alert / Voice / Pain / Unresponsive

2. Orientation

  • Time (day, date, month, year, time of day)
  • Place (hospital, ward, city, country)
  • Person (own name, examiner)

3. Attention and Concentration

  • Digit span (forward ≥6, backward ≥4)
  • Serial 7s subtraction from 100
  • Months of year backwards

4. Memory

  • Immediate: Digit repetition
  • Short-term (recent): 3-object recall at 5 minutes
  • Long-term (remote): Past events, autobiographical

5. Language

TestFinding
Spontaneous speechFluent / Non-fluent
ComprehensionIntact / Impaired (simple and complex commands)
RepetitionIntact / Impaired ("no ifs, ands, or buts")
NamingIntact / Anomia (confrontation naming)
ReadingIntact / Alexia
WritingIntact / Agraphia
Localisation: Broca's (area 44/45, frontal) = non-fluent + intact comprehension; Wernicke's (area 22, temporal) = fluent + impaired comprehension; Conduction = fluent + impaired repetition

6. Praxis

  • Ideomotor: Mimic brushing teeth, combing hair, salute
  • Ideational: Use a key, fold a letter, light a match
  • Constructional: Copy a figure (intersecting pentagons)

7. Visuospatial and Gnosia

  • Clock drawing test
  • Neglect: Line bisection, cancellation test
  • Prosopagnosia / Object agnosia

8. Frontal Lobe Functions

  • Abstraction (similarities/proverbs)
  • Judgement
  • Wisconsin card sorting / MMSE / MoCA (document score)
  • Perseveration / Utilisation behaviour

B. CRANIAL NERVE EXAMINATION

CNNerveTestFinding
IOlfactoryCoffee/soap — each nostril separatelyN / Anosmia / Hyposmia
IIOpticVisual acuity (Snellen), visual fields (confrontation), colour vision, fundoscopyPapilloedema / Optic atrophy
IIIOculomotorPtosis, pupil size + light reflex + accommodation, EOM (up/down/medial)CN III palsy
IVTrochlearDowngaze in adductionSuperior oblique palsy
VTrigeminalFacial sensation (all 3 divisions), corneal reflex, jaw opening + deviation, jaw jerk
VIAbducensLateral gazeLateral rectus palsy
VIIFacialFacial symmetry at rest + on movement; taste anterior 2/3 tongueUMN (forehead spared) vs LMN (Bell's palsy)
VIIIVestibulocochlearWhisper test, Rinne, Weber; nystagmus; Romberg with eyes closed
IX/XGlossopharyngeal / VagusPalate movement (say "aah"), uvula deviation, gag reflex, voice qualityBulbar vs Pseudobulbar
XIAccessorySternocleidomastoid (head turning), trapezius (shoulder shrug against resistance)
XIIHypoglossalTongue at rest (fasciculations?), protrusion (deviation to side of lesion in LMN)

C. MOTOR SYSTEM

1. Inspection

  • Wasting / Hypertrophy (muscle bulk)
  • Fasciculations (LMN, lower motor neurone)
  • Involuntary movements

2. Tone

  • Upper limbs: Clasp-knife spasticity (UMN) / Lead-pipe or cogwheel rigidity (extrapyramidal) / Hypotonia (LMN / cerebellar) / Gegenhalten (frontal)
  • Lower limbs: Clonus — ankle / patellar (≥3 beats = pathological)

3. Power (MRC Grade)

GradeDescription
0No contraction
1Visible contraction only
2Movement with gravity eliminated
3Movement against gravity only
4Movement against resistance (reduced)
5Normal power
Test each group: shoulder, elbow, wrist, fingers (grip, opposition); hip, knee, ankle, toe

4. Reflexes

Deep Tendon Reflexes (DTR)
ReflexRootRightLeft
BicepsC5,C6
SupinatorC5,C6
TricepsC7
Knee (Patellar)L3,L4
Ankle (Achilles)S1,S2
Grade: 0 = absent, + = diminished, ++ = normal, +++ = brisk, ++++ = clonus
Plantar Response (Babinski sign)
  • Right: Flexor / Extensor (UMN sign) / Equivocal
  • Left: Flexor / Extensor / Equivocal
Superficial Reflexes
  • Abdominal reflex: Upper (T8–T10) / Lower (T10–T12) — absent in UMN lesions
  • Cremasteric reflex (males): L1–L2
Primitive Reflexes (if frontal lobe disease suspected)
  • Palmomental / Grasp / Snout / Rooting / Glabellar tap

D. SENSORY SYSTEM

(Always examine with eyes closed; test distal before proximal; compare sides)
ModalityPathwayTestFindings
Pain (pinprick)SpinothalamicDisposable pin
TemperatureSpinothalamicHot/cold tubes
Light touchBothCotton wool
VibrationDorsal column128 Hz tuning fork on bony prominences
Joint position sense (proprioception)Dorsal columnPassive movement of distal phalanx
Two-point discriminationCorticalCalipers
StereognosisCorticalIdentify coin/key by feel
GraphaesthesiaCorticalTrace number on palm
Sensory Level (if spinal cord lesion suspected): Mark highest level of normal sensation on trunk
Dissociated sensory loss: Pain/temperature loss with preserved vibration/JPS = syringomyelia / Brown-Séquard

E. CEREBELLAR SYSTEM

(DANISH — Dysdiadochokinesia, Ataxia, Nystagmus, Intention tremor, Scanning speech, Hypotonia)
TestFinding
Finger-nose testDysmetria / Intention tremor / Past-pointing
Heel-shin testDysmetria
Diadochokinesia (rapid alternating movements)Dysdiadochokinesia
Romberg testPositive in sensory ataxia; negative in cerebellar ataxia
Tandem gait (heel-to-toe)Inability = cerebellar
NystagmusDirection; horizontal / vertical / rotatory
SpeechScanning / Staccato / Explosive
Rebound phenomenonPositive in cerebellar disease

F. GAIT EXAMINATION

Gait TypeFeaturesLocalisation
Hemiplegic / SpasticCircumduction, arm adductedContralateral cortex / capsule
Scissors gaitBoth legs spastic, crossedBilateral UMN
Cerebellar (ataxic)Wide-based, staggering, cannot tandemCerebellum
Sensory ataxicWide-based, worse in dark, Romberg +Dorsal columns
SteppageHigh-stepping (foot drop)Peripheral nerve / LMN
FestinantSmall shuffling steps, stooped, retropulsionBasal ganglia (Parkinsonism)
WaddlingBilateral hip girdle weaknessMyopathy
AntalgicProtective (pain-related)Musculoskeletal

G. AUTONOMIC EXAMINATION

  • Postural BP (lying → standing; drop >20 mmHg systolic = orthostatic hypotension)
  • Bladder distension
  • Sweating asymmetry (Homer's — ipsilateral anhidrosis)
  • Horner's syndrome: Ptosis + Miosis + Anhidrosis + Enophthalmos (sympathetic chain)

H. MENINGEAL SIGNS

SignTechniquePositive if
Neck stiffnessPassive neck flexionResistance to chin-chest approximation
Kernig's signHip 90° flexed → extend kneePain/spasm at <135°
Brudzinski's signFlex neckInvoluntary hip/knee flexion
Jolt accentuationRotate head horizontally 2–3 HzHeadache worsens

I. SPINE EXAMINATION (if cord/radiculopathy suspected)

  • Straight leg raise (SLR): ° at which pain reproduces; Lasègue sign
  • Femoral stretch test: L2–L4 roots
  • Spinal tenderness / Para-spinal muscle spasm
  • Percussion over vertebrae

SECTION 12 — PROVISIONAL DIAGNOSIS

Anatomical Localisation (answer these in order):
  1. Which level? — Cortex / Subcortex / Brainstem / Cerebellum / Spinal cord / Peripheral nerve / Neuromuscular junction / Muscle
  2. Which side? — Left / Right / Bilateral / Crossed (brainstem)
  3. UMN vs LMN?
  4. Single lesion vs multiple lesions?
Provisional Diagnosis: ___________________________________________
Differential Diagnoses:




SECTION 13 — INVESTIGATIONS

Routine

  • CBC, ESR / CRP
  • Blood glucose (RBS/FBS/HbA1c)
  • Renal function tests, Electrolytes (Na, K, Ca, Mg)
  • Liver function tests
  • Lipid profile
  • Thyroid function tests (TSH, T3, T4)
  • Urine routine + microscopy

Neuroimaging

  • CT Brain: Non-contrast first (haemorrhage, calcification); contrast (abscess, tumour)
  • MRI Brain ± Spine: DWI (acute infarct), FLAIR (periventricular lesions), T1+Gad, MRA/MRV
  • CT Angiography / MR Angiography: Vascular lesions

CSF Analysis (after ruling out raised ICP)

ParameterNormalSignificance
Opening pressure70–200 mm H₂ORaised in meningitis, SAH, IIH
Colour / AppearanceColourless, clearXanthochromia = SAH; turbid = bacterial meningitis
Cells0–5 lymphocytes/mm³Pleocytosis
Protein15–45 mg/dLElevated in GBS, MS, infections
Glucose>60% of blood glucoseLow in bacterial/TB/fungal
Gram stain, Culture/Sensitivity
AFB stain / ADATB meningitis
India ink stainCryptococcus
Oligoclonal bandsAbsentMultiple sclerosis

Electrophysiology

  • EEG: Epilepsy, encephalopathy
  • Nerve conduction studies (NCS) + EMG: Peripheral neuropathy, myopathy, NMJ disorder
  • Visual/Brainstem/Somatosensory Evoked Potentials

Special Investigations (targeted)

  • Serum B12, Folate, Thiamine
  • VDRL/TPHA (neurosyphilis)
  • HIV ELISA
  • ANA, Anti-dsDNA, ANCA, Anti-phospholipid antibodies (vasculitis, lupus)
  • Paraneoplastic antibodies (anti-Hu, anti-Yo, anti-NMDAR)
  • Urine porphyrins
  • Serum ceruloplasmin + 24h urine copper (Wilson's disease)
  • Muscle enzymes: CPK, LDH, aldolase

SECTION 14 — MANAGEMENT PLAN

Immediate (Emergency):
  • Airway, Breathing, Circulation
  • GCS < 8 → Consider intubation
  • Seizure → IV Lorazepam → Phenytoin loading
Short-term:
  • Disease-specific treatment
  • Supportive: IV fluids, nasogastric feeding if dysphagia, pressure sore prevention, DVT prophylaxis, catheterisation if retention
Long-term / Rehabilitation:
  • Physiotherapy, Occupational therapy, Speech therapy
  • Antiepileptic therapy, Antiplatelets/anticoagulants, Neuroprotection
  • Bowel and bladder care
  • Psychological support / Counselling

SECTION 15 — PROGNOSIS & DISCUSSION

  • Natural history of the condition
  • Complications anticipated
  • Disability assessment
  • Discussion of case with supervisor
  • Correlation of clinical features with investigations

QUICK LOCALISATION GUIDE (Aide-mémoire)

FeatureLesion Location
Contralateral hemiplegia + hemisensory lossInternal capsule
Hemiplegia + hemianopia + aphasia (dominant)MCA territory
Crossed CN palsy + contralateral hemiplegiaBrainstem
Bilateral pyramidal signs + sensory levelSpinal cord
Ascending paralysis, areflexia, albuminocytological dissociationGBS (peripheral nerve)
Ptosis + diplopia + fatiguable weaknessNeuromuscular junction (Myasthenia gravis)
Proximal weakness + wasting, no sensory lossMyopathy
Cerebellar signs + ipsilateral Horner'sLateral medullary (Wallenberg) syndrome
Resting tremor + cogwheel rigidity + festinant gaitBasal ganglia (Parkinsonism)
Dysdiadochokinesia + nystagmus + scanning speechCerebellar

Sources: Bradley and Daroff's Neurology in Clinical Practice, 8th Ed. | Clinical Medicine, Medicine Postings Standard Framework.

This case sheet covers the full CNS history-taking and examination workflow for medicine postings. Key points to remember:
  • Localise before diagnosing — always answer: which level, which side, UMN or LMN, single or multiple lesion
  • Aura type guides temporal lobe localisation (rising epigastric = mesial temporal; elementary visual = occipital)
  • Risk factors for epilepsy include febrile status epilepticus in infancy, early meningitis/encephalitis, and head trauma — all correlate with specific pathologies
  • Meningeal signs must always be tested in headache + fever presentations
  • CSF analysis after ruling out raised ICP via fundoscopy or neuroimaging

GIT CASE SHEET WITH DETAILED HISTORY TAKING FOR MEDICINE POSTINGS

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GIT case sheet medicine postings detailed history taking abdominal examination proforma MBBS

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Excellent textbook material retrieved. Now I have rich content from Sleisenger & Fordtran's GI and Liver Disease, Yamada's Textbook of Gastroenterology, and Harrison's Principles of Internal Medicine. Let me compile the comprehensive GIT case sheet.

GIT CASE SHEET — MEDICINE POSTINGS

Gastrointestinal System: Detailed History Taking & Examination Proforma


SECTION 1 — PATIENT IDENTIFICATION

FieldDetails
Name
Age / Sex
IP/OP No.
Ward / Bed No.
Occupation
Address
InformantPatient / Relative — Reliability:
Date of Admission
Date of Examination

SECTION 2 — CHIEF COMPLAINTS

(In patient's own words, chronological order with duration)
  1. _____________ — since ___________
  2. _____________ — since ___________
  3. _____________ — since ___________

SECTION 3 — HISTORY OF PRESENTING ILLNESS

"History taking remains the most important component of the initial evaluation of the patient with acute abdominal pain. A large number, if not the majority, of acute abdominal conditions could be diagnosed by considering carefully the history of onset." — Sir Zachary Cope (cited in Sleisenger & Fordtran's GI and Liver Disease)

General Pointers

  • Mode of onset: Sudden / Acute / Sub-acute / Chronic / Insidious
  • Progression: Static / Progressive / Relapsing-remitting / Episodic
  • Course: Improving / Worsening / Fluctuating

A. ABDOMINAL PAIN (If present — SOCRATES)

Site

  • Location and mark on abdomen diagram:
RUQEpigastricLUQ
RLQUmbilical / PeriumbilicalLLQ
SuprapubicDiffuse / GeneralisedLoin
Differential by region (Harrison's, 22nd Ed.):
  • RUQ: Cholecystitis, cholangitis, pancreatitis, hepatitis, Budd-Chiari, pneumonia
  • Epigastric: PUD, GERD, pancreatitis, gastritis, MI (referred), ruptured aortic aneurysm
  • LUQ: Splenic infarct/rupture/abscess, gastric ulcer, pancreatitis
  • RLQ: Appendicitis, Meckel's diverticulum, Crohn's, right ureteric colic, ovarian pathology
  • LLQ: Diverticulitis, colitis, left ureteric colic, sigmoid volvulus
  • Periumbilical: Early appendicitis, mesenteric ischaemia, SBO

Onset

  • Sudden ("thunderclap"/catastrophic): Perforated viscus, ruptured aneurysm, mesenteric ischaemia
  • Acute (minutes–hours): Biliary/renal colic, pancreatitis, appendicitis
  • Gradual: Subacute obstruction, neoplasm, inflammatory bowel disease

Character (Sleisenger & Fordtran)

CauseCharacterRadiation
AppendicitisAching, periumbilical → RLQNone
CholecystitisConstricting, RUQRight scapula
PancreatitisBoring, epigastricMid-back (T10–L2)
DiverticulitisAching, LLQNone
Perforated PUDBurning, epigastric → diffuseNone
SBOCrampy, colicky, periumbilicalNone
Renal/ureteric colicSevere, loin to groinGroin, genitals

Radiation

  • Right shoulder tip / right scapula — biliary / diaphragmatic
  • Mid-back / periscapular — pancreatitis
  • Loin to groin — ureteric colic
  • Interscapular — aortic dissection

Associated features

  • Nausea / Vomiting (projectile vs non-projectile; content — bilious, blood, undigested food)
  • Fever, rigors — infection (cholangitis, appendicitis, peritonitis)
  • Jaundice — hepatobiliary
  • Change in bowel habits
  • Distension
  • Haematemesis / Melaena / Haematochezia

Timing & duration

  • Constant vs colicky (intermittent, crampy = hollow viscus obstruction)
  • Duration of each episode
  • Diurnal variation: Peptic ulcer — hunger pain / nocturnal pain

Severity (VAS 1–10)

  • Effect on daily activity / sleep

Aggravating and Relieving factors

  • Food: Pain worsened by eating → gastric ulcer, mesenteric ischaemia; Pain relieved by food/antacids → duodenal ulcer
  • Posture: Leaning forward relieves pancreatitis pain
  • Defaecation relieves — IBS, colonic pathology
  • Menstrual cycle — endometriosis, ovarian pathology

Previous episodes

  • Similar episodes in the past? Treatment received? Investigations done?

B. DYSPHAGIA / ODYNOPHAGIA

"Patients almost invariably recognize accurately the locus and consequence of oropharyngeal dysphagia; they mistakenly identify the neck as the locus of bolus hang-up with esophageal dysphagia about 30% of the time." — Yamada's Textbook of Gastroenterology, 7th Ed.

Localisation

  • Oropharyngeal dysphagia: Difficulty initiating swallow, coughing, choking, nasopharyngeal regurgitation, drooling, aspiration → Neurological/muscular cause (CVA, MND, myasthenia)
  • Esophageal dysphagia: Sensation of food sticking after swallowing → Structural or motility disorder

Nature

  • Solids only → progressing to liquids: Mechanical obstruction (carcinoma oesophagus, peptic stricture, Schatzki ring)
  • Solids AND liquids from onset: Motility disorder (achalasia, oesophageal spasm)
  • Liquids > Solids: Neuromuscular (oropharyngeal)
  • Intermittent: Motility disorder, Schatzki ring
  • Progressive: Carcinoma (red flag)

Associated symptoms

  • Odynophagia (painful swallowing): Oesophageal ulcer, infective oesophagitis (Candida, CMV, HSV), eosinophilic oesophagitis
  • Regurgitation of undigested food: Pharyngeal pouch (Zenker's diverticulum), achalasia
  • Heartburn / Acid reflux (GERD → peptic stricture)
  • Weight loss (malignancy — red flag)
  • Hoarseness (recurrent laryngeal nerve involvement by tumour)
  • Hiccups (diaphragmatic/mediastinal involvement)
  • Respiratory symptoms: Aspiration pneumonia, nocturnal cough

Globus Sensation

  • Painless lump/foreign body sensation in throat between meals (unlike dysphagia which occurs only during swallowing)
  • Associated with GERD, motility disorder, anxiety

C. HEARTBURN / GASTRO-OESOPHAGEAL REFLUX

  • Burning sensation: Retrosternal / epigastric, radiating upward to throat / mouth
  • Timing: Post-prandial, on bending forward, on lying down, nocturnal
  • Aggravated by: Fatty food, chocolate, coffee, alcohol, smoking, NSAIDs, large meals
  • Relieved by: Antacids, sitting up, water
  • Regurgitation: Sour / bitter fluid, "water brash" (excess salivation)
  • Chronic cough, hoarseness, throat clearing (extra-oesophageal GERD)
  • Dysphagia superimposed: Suggests peptic stricture or Barrett's (red flag)

D. NAUSEA AND VOMITING

  • Onset: Sudden vs gradual
  • Timing: Morning (pregnancy, alcoholic gastritis, raised ICP), post-prandial (pyloric obstruction), projective
  • Content:
    • Undigested food: Oesophageal/gastric cause
    • Partially digested + bile: Duodenal/intestinal
    • Faeculant (faecal smell): Low intestinal obstruction
    • Blood (haematemesis): See below
  • Volume and frequency
  • Relationship to pain: Vomiting relieves pain of SBO; does not relieve pancreatitis/appendicitis
  • Associated features: Vertigo (labyrinthine), headache/photophobia (migraine), diarrhoea (gastroenteritis)
  • Dehydration assessment: Thirst, decreased urine output, sunken eyes

E. HAEMATEMESIS AND MELAENA (Upper GI Bleed)

  • Haematemesis: Vomiting of blood
    • Fresh red blood: Active arterial bleed (varices, Mallory-Weiss tear)
    • Coffee-ground material: Altered blood (PUD, gastric erosions)
  • Melaena: Black, tarry, offensive-smelling stools — blood from proximal GIT (>50 mL)
  • Haematochezia: Bright red blood per rectum (LGIB or massive UGIB)

History for UGI Bleed:

  • Peptic ulcer: Previous PUD history, NSAIDs use, aspirin, steroids, H. pylori (dyspepsia, epigastric pain)
  • Varices: Liver disease history (alcohol, hepatitis, jaundice, previous variceal bleed, cirrhosis)
  • Mallory-Weiss tear: Forceful vomiting preceding haematemesis
  • Malignancy: Weight loss, anorexia, dysphagia
  • Anticoagulants / Antiplatelets: Warfarin, aspirin, clopidogrel, NSAIDs
  • Quantity of blood: Teaspoon / Cup / Bowl estimate; associated dizziness/syncope (haemodynamic compromise)
  • Previous similar episodes

F. HAEMATOCHEZIA / RECTAL BLEEDING (Lower GI Bleed)

  • Nature of blood:
    • Blood mixed with stool: Colonic source (carcinoma, IBD, diverticular)
    • Blood on surface of stool / on toilet paper: Anorectal (haemorrhoids, fissure)
    • Blood separate from stool: Polyp, angiodysplasia
    • Mucus + blood: IBD (ulcerative colitis), infective colitis, carcinoma
  • Associated features: Tenesmus, urgency, change in bowel habit, weight loss
  • Anal symptoms: Pain on defaecation (fissure), prolapse, pruritus ani

G. DIARRHOEA

  • Duration: Acute (<2 weeks) vs Chronic (>4 weeks)
  • Stool characteristics:
    • Watery (large volume, no blood): Secretory/osmotic, small intestinal origin
    • Bloody (small volume + mucus + urgency): Inflammatory, large intestinal origin
    • Fatty / Oily / Frothy / Foul-smelling (floats): Steatorrhoea — malabsorption
    • Pale/clay-coloured: Obstructive jaundice / Exocrine pancreatic insufficiency
  • Frequency (per day) and volume per episode
  • Nocturnal diarrhoea: Organic (IBD, diabetic autonomic neuropathy) — rules out IBS
  • Associated symptoms: Abdominal cramps, urgency, tenesmus, fever, weight loss
  • Food history: Dietary triggers (osmotic); onset after specific meal (infective)
  • Contact history / Travel history: Infective gastroenteritis, tropical sprue
  • ETOH use: Alcoholic pancreatitis, exocrine insufficiency
  • Medications: Antibiotics (C. difficile), metformin, laxatives, PPI
Secretory vs Osmotic diarrhoea:
FeatureSecretoryOsmotic
FastingDiarrhoea persistsDiarrhoea stops
Osmotic gap<50 mOsm/kg>125 mOsm/kg
ExampleCholera, VIPomaLactose intolerance, laxative

H. CONSTIPATION

  • Definition: <3 stools/week or hard/straining/incomplete evacuation
  • Duration: Acute (obstruction, colonic carcinoma) vs Chronic (IBS, functional)
  • Onset: Sudden change (red flag — colonic malignancy)
  • Stool calibre: Ribbon-like (rectal carcinoma)
  • Associated symptoms: Bloating, abdominal distension, overflow diarrhoea
  • Straining, incomplete evacuation, manual disimpaction required
  • Rectal bleeding / Mucus: Carcinoma, solitary rectal ulcer
  • Systemic causes: Hypothyroidism, hypercalcaemia, Parkinson's, opiate use, anticholinergics
  • Dietary: Low fibre intake, inadequate fluids
  • Alternating constipation and diarrhoea: IBS, carcinoma of colon

I. JAUNDICE

  • Onset: Sudden vs gradual
  • Duration
  • Type by history:
FeaturePre-hepatic (Haemolytic)Hepatic (Hepatocellular)Post-hepatic (Obstructive/Cholestatic)
Urine colourNormalDark (bilirubinuria)Dark (bilirubin)
Stool colourNormal or darkNormal or palePale/clay-coloured
PruritusAbsentVariableProminent
PainAbsentDull hepatic painColicky RUQ (stone) / Dull (malignancy)
FeverAbsentPresent (hepatitis)High with rigors (cholangitis)
  • Dark urine (cola/tea-coloured): Conjugated bilirubin — hepatic or post-hepatic
  • Pale/clay stools: Obstruction of biliary outflow
  • Pruritus: Bile salt deposition in skin (cholestasis)
  • Risk factors:
    • Viral hepatitis: Contaminated food/water (HAV, HEV), blood/sexual exposure (HBV, HCV, HDV)
    • Alcohol history (alcoholic hepatitis)
    • Blood transfusions, IV drug use, tattoos, unprotected sexual intercourse
    • Travel to endemic area
    • Family history of liver disease / jaundice
    • Medications (paracetamol, isoniazid, rifampicin, statins, oral contraceptives)
    • Auto-immune history

J. ASCITES / ABDOMINAL DISTENSION

  • Duration and progression
  • Associated features: Bilateral leg oedema, breathlessness (large ascites / hepatic hydrothorax), scrotal oedema
  • Causes by history:
    • Cirrhosis: Alcohol, viral hepatitis, NASH — previous liver disease, jaundice, haematemesis
    • Malignancy: Wasting, prior cancer, lymphadenopathy
    • Cardiac: Bilateral oedema, exertional dyspnoea, orthopnoea (congestive heart failure)
    • Renal: Frothy urine, facial puffiness, nephrotic syndrome
    • Tuberculosis: Fever, night sweats, weight loss, cough, contact
  • SAAG (Serum-Ascites Albumin Gradient): ≥1.1 g/dL = portal hypertension related

K. WEIGHT LOSS AND ANOREXIA

  • Quantity and time period: kg lost over months
  • Unintentional vs intentional
  • Appetite: Decreased (malignancy, malabsorption, depression) vs maintained (malabsorption, hyperthyroidism)
  • Food intake: Change in dietary habits
  • Associated symptoms: Diarrhoea (malabsorption), dysphagia (oesophageal Ca), jaundice (pancreatic Ca), night sweats, fever (malignancy, TB)
  • RED FLAGS for GI malignancy:
    • Age >50, unintentional weight loss, progressive dysphagia
    • Haematemesis, melaena, haematochezia
    • Persistent vomiting, iron-deficiency anaemia
    • Palpable mass, organomegaly
    • New onset dyspepsia in >55 years

L. DYSPEPSIA AND PEPTIC ULCER DISEASE

  • Epigastric pain / discomfort:
    • Duodenal ulcer: Hunger pain 2–4 hours post-meal, relieved by food/antacids, nocturnal pain (2–4 AM)
    • Gastric ulcer: Pain immediately/shortly after eating, not relieved by food
  • Bloating, early satiety (delayed gastric emptying)
  • NSAID/aspirin use: Dose, duration, with or without food
  • H. pylori risk: Socioeconomic status, household contacts with peptic ulcer
  • Alcohol and smoking: Impair mucosal defence
  • Acid regurgitation, belching

SECTION 4 — PAST HISTORY

ConditionDetails
Similar episodes previouslyYes / No; investigations/treatment
Peptic ulcer disease / GERDYes / No; H. pylori treatment
Liver disease (hepatitis, cirrhosis)Yes / No; aetiology, Child-Pugh class
PancreatitisYes / No; acute/chronic, cause
IBD (Crohn's / UC)Yes / No; extent, medications
GI malignancyYes / No; treatment
Surgeries (GI)Cholecystectomy, appendicectomy, bowel resection, colostomy, previous endoscopy findings
Blood transfusionsYes / No
Jaundice / HepatitisYes / No; type, treatment
Tuberculosis (abdominal TB)Yes / No
Diabetes mellitusYes / No (gastroparesis, NASH, diarrhoea)
Thyroid diseaseYes / No (constipation in hypothyroidism)
Cardiac diseaseYes / No (Budd-Chiari, congestive hepatopathy, ischaemic colitis)
Drug allergies

SECTION 5 — FAMILY HISTORY

  • Peptic ulcer disease / H. pylori infection
  • Colorectal carcinoma (first-degree relative <50 years — FAP, HNPCC/Lynch syndrome)
  • Inflammatory bowel disease (genetic predisposition)
  • Pancreatitis (hereditary)
  • Viral hepatitis (HBV — vertical transmission)
  • Liver disease, cirrhosis
  • Coeliac disease (HLA-DQ2/DQ8 association)
  • Polyp syndromes (FAP, Peutz-Jeghers, juvenile polyposis)
  • Haemochromatosis, Wilson's disease (autosomal recessive)

SECTION 6 — PERSONAL HISTORY

ItemDetails
DietVegetarian / Non-vegetarian; spicy / fatty food; fibre intake; regular meals
AppetiteNormal / Decreased (malignancy, depression) / Increased
Bowel habit baselineFrequency, consistency (Bristol Stool Chart 1–7)
MicturitionDark urine, frothy urine, haematuria
SleepDisturbed by pain (nocturnal PUD, pancreatitis)
AlcoholYes / No; type, quantity, frequency, duration; binge vs daily (Units/week: >14 F, >21 M = harmful)
SmokingYes / No; pack-years (risk factor: PUD, Crohn's, pancreatic Ca, oesophageal Ca)
Illicit drugsIV drug use (hepatitis B/C transmission)
OccupationExposure to hepatotoxins, aflatoxin (hepatocellular carcinoma)
Marital / Sexual historyHBV/HCV/HIV transmission risk
Travel historyEndemic areas: Amoebiasis, typhoid, hepatitis A/E, cholera, intestinal TB, strongyloidiasis

SECTION 7 — TREATMENT HISTORY

  • Current medications (NSAIDs, aspirin, steroids, antibiotics, PPIs, anticoagulants, immunosuppressants)
  • Hepatotoxic drugs (paracetamol, isoniazid, rifampicin, methotrexate, statins, OCPs)
  • Previous endoscopy / colonoscopy results
  • Prior surgeries and outcomes
  • Traditional / Herbal medicines (hepatotoxic)

SECTION 8 — MENSTRUAL HISTORY (Females)

  • Last menstrual period (LMP) — rule out ectopic pregnancy in RLQ/LLQ pain
  • Cycle regularity
  • Dysmenorrhoea / Dyspareunia — endometriosis
  • Amenorrhoea — pregnancy, ovarian cyst torsion
  • Vaginal discharge / Pelvic inflammatory disease

SECTION 9 — GENERAL PHYSICAL EXAMINATION

Vitals

ParameterValue
Pulse/min; rhythm; volume
BPmmHg; postural drop
Temperature°F (fever in cholangitis, peritonitis, IBD, infective colitis)
Respiratory Rate/min
Weightkg
BMIkg/m² (obesity → NAFLD, GERD, gallstones)

General Examination

  • Built and nourishment: Wasted (malignancy, malabsorption, IBD, cirrhosis) / Obese (NAFLD, gallstones)
  • Pallor: Iron deficiency anaemia (chronic GI blood loss), haemolysis (haemolytic jaundice)
  • Icterus / Jaundice: Scleral icterus (earliest sign at bilirubin >2.5 mg/dL)
  • Clubbing: Liver cirrhosis, Crohn's disease, GI lymphoma, coeliac disease
  • Leukonychia (white nails): Hypoalbuminaemia (cirrhosis)
  • Palmar erythema: Liver disease, pregnancy
  • Dupuytren's contracture: Alcoholic liver disease
  • Spider naevi (>5 = pathological): Liver disease; look in SVC drainage area (face, neck, chest, arms)
  • Parotid enlargement: Alcoholism
  • Gynaecomastia / Testicular atrophy: Cirrhosis (hyperoestrogenaemia)
  • Asterixis (liver flap / flapping tremor): Hepatic encephalopathy — ask patient to dorsiflex wrists for 15 seconds
  • Lymphadenopathy:
    • Virchow's node (left supraclavicular) — gastric carcinoma (Troisier's sign)
    • Periumbilical — Sister Mary Joseph nodule (intra-abdominal malignancy)
    • Axillary — Irish's node (gastric carcinoma)
  • Peripheral oedema: Bilateral pitting — hypoalbuminaemia (cirrhosis, malabsorption, nephrotic syndrome), CCF
  • Skin:
    • Jaundice
    • Scratch marks (pruritus of cholestasis)
    • Xanthelasma / Xanthomata (primary biliary cholangitis, hyperlipidaemia)
    • Erythema nodosum / Pyoderma gangrenosum (IBD)
    • Dermatitis herpetiformis (coeliac disease)
    • Peutz-Jeghers pigmentation (perioral, buccal mucosa, digits)
    • Acanthosis nigricans (GI malignancy, insulin resistance)
    • Bronze pigmentation (haemochromatosis)
    • Kayser-Fleischer rings in eyes (Wilson's disease)
  • Fetor hepaticus: Sweet musty breath (liver failure / portosystemic shunting)

SECTION 10 — ABDOMINAL EXAMINATION

Surface Anatomy Reference

(Mark on diagram: 9 regions / 4 quadrants)
Nine regions: Right hypochondrium | Epigastrium | Left hypochondrium | Right lumbar | Umbilical | Left lumbar | Right iliac fossa | Hypogastrium/Pubic | Left iliac fossa

INSPECTION

(Patient supine, exposed from xiphisternum to pubis, arms by sides, knees slightly flexed)
FindingSignificance
Shape / ContourScaphoid (wasting, peritonitis) / Distended (ascites, obstruction, organomegaly, flatus)
SymmetryAsymmetric distension — localised mass / organomegaly
UmbilicusEverted (ascites, large tumour) / Inverted (normal) / Displaced
SkinDilated veins, jaundice, scar marks, striae
Dilated veinsCaput medusae (portal hypertension — blood flows away from umbilicus); IVC obstruction (blood flows upward on both flanks)
ScarsPrevious laparotomy, cholecystectomy, transplant, colostomy, ileostomy
StomaColostomy (left, formed stool) / Ileostomy (right, liquid stool)
Visible peristalsisGastric outlet obstruction (epigastric); intestinal obstruction (ladder pattern)
PulsationEpigastric pulsation — aortic aneurysm, transmitted aortic pulsation
HerniaeUmbilical, incisional, inguinal, femoral — look for impulse on coughing
Abdominal movement with respirationAbsent/restricted = peritonitis

PALPATION

(Always begin away from the point of maximum tenderness; warm hands; watch patient's face)

Superficial Palpation

  • Guarding (voluntary / involuntary)
  • Rigidity (board-like = perforated viscus / peritonitis)
  • Tenderness: Site, severity, local vs diffuse

Deep Palpation

  • Masses: Site, size, shape, surface, consistency, margins, mobility, pulsatility, tenderness, plane
  • Hepatomegaly (see below)
  • Splenomegaly (see below)

LIVER EXAMINATION

  • Technique: Start from RIF, move towards RUQ; percuss upper border first
  • Size: Span (normal <12.5 cm in MCL); measure in cm below costal margin at MCL
  • Surface: Smooth (hepatitis, CCF, fatty liver) / Nodular (cirrhosis, metastases)
  • Consistency: Soft / Firm / Hard
  • Tenderness: Tender — hepatitis, CCF, acute amoebic abscess; Non-tender — cirrhosis, malignancy
  • Edge: Rounded (CCF, fatty liver) / Sharp and firm (cirrhosis)
  • Pulsatility: Pulsatile — tricuspid regurgitation
  • Hepatic rub: Hepatocellular carcinoma over the surface
Causes by consistency:
ConsistencyCauses
Soft, tenderHepatitis, CCF (congestive hepatopathy), amoebic abscess
Firm, non-tenderCirrhosis, fatty liver
Hard, irregularHCC, metastases
PulsatileTricuspid regurgitation

SPLENOMEGALY EXAMINATION

  • Technique: Start from RIF, move to LUQ; cannot "get above it"; moves with respiration; notch medially; dull on percussion; not ballottable
  • Grades:
    • Grade I (mild): Palpable only on deep inspiration
    • Grade II (moderate): Extends to umbilical line
    • Grade III (massive): Below umbilicus / to RIF (malaria, myelofibrosis, CML, kala-azar, Gaucher's)
Causes of massive splenomegaly (mnemonic: MMKGC — Myelofibrosis, Malaria, Kala-azar, Gaucher's, CML)

KIDNEY / RENAL EXAMINATION

  • Ballottement: Place one hand behind loin (posteriorly), push upward; palpate anteriorly
  • Distinguishing kidney from spleen: Ballottable, no notch, resonant on percussion (gas-filled bowel anterior), can get above it

ASCITES EXAMINATION

  • Shifting dullness: Percuss from umbilicus to flank until dull → keep finger there → roll patient 45° away → re-percuss (becomes resonant if shifting = ascites ≥1.5 L)
  • Fluid thrill: One hand on flank, flick opposite flank — felt if large ascites (place other hand/assistant's hand on midline to damp transmission through fat)
  • Dipping (ballottement): Large ascites — quick, jabbing palpation to feel organ through fluid

SPECIAL SIGNS

SignTechniquePositive findingSignificance
Murphy's signDeep inspiration while fingers press below RCMArrest of inspiration due to painAcute cholecystitis
Courvoisier's signPalpable, non-tender GBPainless jaundice + palpable GBCarcinoma head of pancreas (NOT gallstones — fibrosis prevents distension)
Rovsing's signPressure in LIF → pain in RIFReferred RIF painAppendicitis
McBurney's point1/3 from ASIS to umbilicusMaximal tendernessAppendicitis
Psoas signHip extension with patient on left sideRIF painRetrocaecal appendicitis / Psoas abscess
Obturator signHip flexion + internal rotationHypogastric painPelvic appendicitis / Pelvic abscess
Carnett's signTense abdomen by raising head → palpateTenderness increasesAnterior abdominal wall pain (not visceral)
Rebound tendernessGentle percussion / coughWorse on releasePeritoneal inflammation

PERCUSSION

  • General percussion: Dullness (organomegaly, mass, ascites) / Resonance (gas-filled bowel)
  • Liver dullness: Upper border (5th IC space MCL) to lower border
  • Traube's space: 6th rib above, MAL laterally, costal margin below — normally resonant (gastric air bubble); Dull = splenomegaly / pleural effusion
  • Bladder: Suprapubic dullness (retention)

AUSCULTATION

  • Bowel sounds:
    • Normal: 5–10/min, low-pitched
    • Increased (high-pitched, tinkling): Intestinal obstruction ("borborygmi")
    • Absent (silent abdomen): Paralytic ileus, peritonitis
  • Succussion splash: Large fluid-gas level in stomach — pyloric stenosis / gastric outlet obstruction (>4 hours post-meal)
  • Bruits:
    • Epigastric: Renal artery stenosis (renovascular hypertension), aortic aneurysm
    • Hepatic bruit: Hepatocellular carcinoma, hepatic AVM, alcoholic hepatitis
    • Splenic friction rub: Splenic infarct, perisplenitis

RECTAL EXAMINATION (PR)

(Always offer explanation, chaperone, consent)
  • Inspection: Haemorrhoids (grade), fistula, fissure, skin tags, condylomata
  • Tone: Reduced (spinal cord lesion), increased (fissure)
  • Contents: Faecal impaction, blood (glove)
  • Masses: Rectal carcinoma (shelf of rock-hard tissue), polyp
  • Prostate (males): Size, surface, consistency, median sulcus
  • Uterus / Cervix (females)
  • Pelvic peritoneum: Boggy, tender (pelvic abscess — "pelvic peritonitis to feel by PR")
  • After PR — inspect glove: Blood / Melaena / Mucus / Pale stools / Pus

SECTION 11 — SYSTEMIC EXAMINATION

Cardiovascular:

  • AF (mesenteric ischaemia, portal vein thrombosis)
  • Murmurs (carcinoid — pulmonary/tricuspid)
  • JVP elevation (congestive hepatopathy)

Respiratory:

  • Pleural effusion (pancreatitis — left side; massive ascites — hepatic hydrothorax)
  • Consolidation (aspiration, pneumonia mimicking acute abdomen)
  • Lung metastases (colonic carcinoma)

Musculoskeletal:

  • Arthritis (IBD — enteropathic arthritis; Whipple's disease; reactive arthritis)
  • Clubbing (IBD, cirrhosis)

Neurological:

  • Hepatic encephalopathy: Asterixis, altered GCS, fetor hepaticus
  • Peripheral neuropathy: Vitamin B12/B1 deficiency (malabsorption, alcoholism)
  • Proximal myopathy: IBD, malabsorption (Vitamin D)

SECTION 12 — PROVISIONAL DIAGNOSIS & DIFFERENTIAL DIAGNOSIS

Provisional Diagnosis: ___________________________________________
Differential Diagnoses:




SECTION 13 — INVESTIGATIONS

Routine Blood Tests

  • CBC (anaemia, leucocytosis, thrombocytopenia in hypersplenism)
  • ESR / CRP (inflammation, IBD, malignancy)
  • Blood glucose, HbA1c (diabetes → gastroparesis, NAFLD)
  • LFTs: Total/direct/indirect bilirubin, AST, ALT, ALP, GGT, total protein, albumin
  • Renal function tests + electrolytes (dehydration, hepatorenal syndrome, prerenal AKI)
  • Coagulation: PT, INR (liver synthetic function)
  • Amylase / Lipase (pancreatitis — lipase more specific)
  • Lipid profile (gallstones, NAFLD)
  • Thyroid function tests (TSH — constipation/diarrhoea)

Liver Disease Panel

  • Hepatitis B surface antigen (HBsAg), Anti-HBs, Anti-HBc (IgM/IgG), HBeAg
  • Anti-HCV antibody + HCV RNA (PCR)
  • Anti-HAV IgM / Anti-HEV IgM
  • Serum ferritin + transferrin saturation (haemochromatosis)
  • Serum ceruloplasmin + 24h urine copper (Wilson's disease)
  • ANA, Anti-smooth muscle antibody (ASMA), AMA (autoimmune hepatitis / PBC)
  • AFP (alpha-fetoprotein) — HCC screening
  • Child-Pugh score + MELD score (cirrhosis staging)

Stool Examination

  • Routine: Colour, consistency, mucus, blood, parasites
  • Microscopy: Ova, cysts, trophozoites, fat globules (malabsorption)
  • Culture + sensitivity
  • C. difficile toxin (pseudomembranous colitis)
  • Faecal occult blood (FOBT) — colon cancer screening
  • Faecal calprotectin (IBD vs IBS — elevated in IBD)
  • Sudan staining for fat (steatorrhoea)

Urine

  • Bilirubin (conjugated jaundice)
  • Urobilinogen (absent in complete obstruction; increased in haemolysis/hepatitis)

Radiology

  • X-ray Abdomen (Erect + Supine):
    • Air under diaphragm (erect) — perforated viscus
    • Dilated bowel loops + air-fluid levels — obstruction (SBO vs LBO)
    • Gallstones (10% radio-opaque), renal calculi, pancreatic calcification
    • Absent psoas shadow (retroperitoneal pathology)
  • Ultrasound Abdomen:
    • Gallstones, biliary dilatation (CBD >6 mm)
    • Liver: Size, echogenicity, nodularity, portal vein diameter (>13 mm = PH)
    • Spleen size, ascites (free fluid), lymph nodes, masses
    • Pancreas
  • CT Abdomen with contrast:
    • Pancreatitis severity (Balthazar score)
    • Abdominal mass characterisation
    • IBD extent (Crohn's complications — fistulae, abscess)
    • Staging of GI malignancy
  • MRI / MRCP: Biliary and pancreatic ductal anatomy (choledocholithiasis, PSC, chronic pancreatitis)
  • CECT/Angiography: GI bleed localisation, mesenteric ischaemia

Endoscopy

  • Upper GI Endoscopy (OGD): Oesophageal varices, PUD, gastric Ca, oesophageal Ca, GERD, mucosal biopsy
  • Colonoscopy: IBD, CRC screening, polyps, diverticular disease, biopsy
  • Flexible Sigmoidoscopy: Distal colonic pathology
  • ERCP: Therapeutic: Stone removal, stenting; Diagnostic: Biliary/pancreatic ductal disease
  • Endoscopic Ultrasound (EUS): Pancreatic masses, submucosal lesions, biliary pathology

Special Investigations (targeted)

InvestigationIndication
H. pylori (urea breath test / stool antigen / endoscopic biopsy)PUD, gastric MALT lymphoma
Serum B12, Folate, Iron studiesMalabsorption, anaemia
Anti-tTG IgA + IgG (tissue transglutaminase)Coeliac disease
ANCA (pANCA, ASCA)IBD differentiation (UC vs Crohn's)
Serum gastrinZollinger-Ellison syndrome
24h oesophageal pH monitoring ± manometryGERD, motility disorders
Scintigraphy (gastric emptying scan)Gastroparesis
Hydrogen breath testSIBO, lactose/fructose intolerance
D-Xylose absorption testMucosal vs pancreatic malabsorption
Faecal elastaseExocrine pancreatic insufficiency
Serum CA 19-9, CEAPancreatic Ca, CRC (monitoring)
Diagnostic ascitic tap (paracentesis)Ascites characterisation

Ascitic Fluid Analysis

ParameterTransudative (SAAG ≥1.1)Exudative (SAAG <1.1)
CausePortal hypertension, CCF, Budd-ChiariTB, malignancy, pancreatitis, nephrotic syndrome
Protein<25 g/L>25 g/L
LDHLowHigh
Cells<250/mm³ PMN (<250)>500/mm³ (SBP if PMN ≥250)
SpecialCulture (SBP), cytology (malignancy), ADA (TB)

SECTION 14 — MANAGEMENT PLAN

Immediate (Emergency):
  • Haemodynamic resuscitation: IV access (2 large bore) → IV fluids / blood products
  • NBM in GI bleed / surgical abdomen
  • IV PPI (omeprazole/pantoprazole) in UGIB
  • Endoscopy (urgent OGD within 24h in UGIB)
  • Surgical consult if: Peritonitis, perforation, obstruction
Short-term / Targeted:
  • Disease-specific: Antibiotics (cholangitis, SBP, infective colitis), antivirals (hepatitis B/C), immunosuppressants (IBD), PPIs (H. pylori triple therapy)
  • Nutritional support: High-protein diet (unless hepatic encephalopathy), vitamins
  • Alcohol cessation (counselling, thiamine, benzodiazepines for withdrawal)
  • Diuretics (spironolactone + frusemide for ascites)
  • Beta-blockers (propranolol — variceal prophylaxis)
Long-term:
  • Surveillance endoscopy (Barrett's, varices, cirrhosis — HCC screening USG 6-monthly + AFP)
  • Colonoscopy surveillance (IBD, CRC after polyp removal)
  • Dietary modifications (low-salt for ascites, high-fibre for constipation, gluten-free for coeliac)
  • Rehabilitation (alcohol, nutritional)

SECTION 15 — PROGNOSIS & DISCUSSION

  • Natural history of the condition
  • Complications anticipated
  • Scoring systems used (Child-Pugh, MELD, Ranson's/APACHE for pancreatitis, Harvey-Bradshaw for Crohn's, Mayo score for UC)
  • Correlation of clinical findings with investigations
  • Discussion with supervisor

QUICK LOCALISATION & DIAGNOSIS GUIDE

Symptom ClusterLikely Diagnosis
Hunger pain + nocturnal pain + relief by foodDuodenal ulcer
Pain immediately after food + no reliefGastric ulcer
Haematemesis + alcohol + known liver diseaseOesophageal varices
Coffee-ground vomit + NSAID use + epigastric tendernessPeptic ulcer bleed
Painless jaundice + palpable GB (Courvoisier's)Carcinoma head of pancreas
Jaundice + fever + RUQ pain (Charcot's triad)Cholangitis
Epigastric boring pain → back + raised amylase/lipaseAcute pancreatitis
Periumbilical pain → RIF migration + anorexia + low-grade feverAcute appendicitis
Bloody diarrhoea + tenesmus + urgencyUlcerative colitis / Infective colitis
Non-bloody watery diarrhoea + skip lesions + perianal diseaseCrohn's disease
Ascites + caput medusae + splenomegaly + spider naeviPortal hypertension / Cirrhosis
Alternating constipation + diarrhoea + bloating + no nocturnal symptomsIBS
Progressive dysphagia (solids → liquids) + weight loss + age >50Oesophageal carcinoma
Massive splenomegalyCML, kala-azar, myelofibrosis, malaria

Sources: Sleisenger and Fordtran's Gastrointestinal and Liver Disease, 11th Ed. | Yamada's Textbook of Gastroenterology, 7th Ed. | Harrison's Principles of Internal Medicine, 22nd Ed. (2025) | Standard GIT Medicine Posting Framework.

Key points to remember for medicine postings:
  • "The history is the most important part" — Sir Zachary Cope's dictum still holds for acute abdomen
  • Always check SAAG in ascites (≥1.1 = portal hypertension related)
  • Courvoisier's Law: Palpable painless GB with jaundice = NOT gallstones = malignancy
  • Melaena vs Haematochezia: Melaena = upper GI source; fresh red blood (haematochezia) in massive UGIB can also occur
  • Red flags in GI: Age >50, weight loss, progressive dysphagia, rectal bleeding, new-onset dyspepsia >55 years, palpable mass, iron-deficiency anaemia — warrant urgent investigation
  • In jaundice, always check for stigmata of chronic liver disease before ascribing a cause
  • Child-Pugh score (bilirubin, albumin, INR, ascites, encephalopathy) — classify cirrhosis A/B/C

CVS CASE SHEET WITH DETAILED HISTORY TAKING FOR MEDICINE POSTINGS

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