Fig. 5D.62: Reitan’s number-connection test.
Types of hepatorenal syndromes (HRS)
Type 1 hepatorenal syndrome Type 2 hepatorenal syndrome
It is characterized by progressive oliguria, a rapid
rise of the serum creatinine to above 2.5 mg/dL
and has a very poor prognosis
Usually precipitated by spontaneous bacterial
peritonitis Without treatment, median survival is less than 1 month and almost all patients die within 10 weeks
after the onset of renal failure
It is characterized by a reduction in glomerular filtration, moderate and
stable increase in serum creatinine (>1.5 mg/dL), but it is fairly stable
and has a better prognosis than Type 1 HRS
Usually occurs in patients with refractory ascites (resistant to diuretics)
Median survival is 3–6 months
Precipitating factors for hepatorenal syndrome
Gastrointestinal bleeding
Aggressive paracentesis
Diuretic therapy
Sepsis including spontaneous bacterial peritonitis
Diarrhea
SITES OF PORTOSYSTEMIC ANASTOMOSIS (FIG. 5D.63)
Fig. 5D.63: Sites of portosystemic anastomosis in cirrhosis.
CLASSIFICATION OF PORTAL HYPERTENSION (FIG. 5D.64)
Fig. 5D.64: Classification of portal hypertension according to site of vascular obstruction.
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A. CASE SHEET FORMAT
HISTORY TAKING
Name:
Age:
Sex:
Residence:
Occupation:
Chief complaints:
________ × days
________ × days
________ × days
History of presenting illness:
HIGHER MENTAL FUNCTION
Altered state of consciousness:
Onset
Any seizures and blackouts
Any fall/injuries
Any ear or nose bleed
Fever
Any ear pain or discharge
Drug history
Any addictions.
Mental state and cognition:
Changes in the memory
State of alertness and drowsiness
Changes in the mood and affect (loss of spontaneity)
Language changes
Loss of spatial orientation
Diminished ability to carry out routine activities of daily living.
Other higher mental functions:
Speech difficulty
Difficulty to recognize people or objects
Inappropriate crying or laughter
Lack of interest
Social disinhibition
Delusions/hallucinations.
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CRANIAL NERVE DYSFUNCTION
Ask about:
Loss of vision, smell, and taste
Alteration in facial feeling
Double vision/visual symptoms
Problems with swallowing and chewing
Speech alterations
Vertigo/hearing abnormalities
Hoarseness of voice, dysphagia, nasal regurgitation, and nasal intonation of speech
Pain/difficulty in neck movements.
Example
Left lower motor neuron (LMN) 7th nerve palsy: History of retroauricular pain followed by abrupt
onset deviation of angle of mouth to right with slurring of speech and difficulty in left eye closure
with history of hyperacusis.
MOTOR DYSFUNCTION
Weakness
Distribution of weakness:
Is it symmetrical/asymmetric:
Paresis or plegia:
Limbs involved:
Ipsilateral or contralateral:
Patterned weakness.
Example
Right middle cerebral artery (MCA) territory embolic infarct: History of sudden onset, complete loss
of power in left upper limb and lower limb. Weakness maximum at onset and nonprogressive.
Onset and progression:
Acute, subacute, or chronic
Progression of the weakness:
Ascending weakness or descending weakness
Ellsberg phenomenon
Variation throughout the day
Muscles/limb(s) involved.
Proximal upper limb—
shoulder/arm:
Difficulties in combing hair, reaching for high objects, winging of scapula
Distal upper limb—forearm/hand: Finger/wrist drop, poor hand grip, cannot open jar, difficulty in
buttoning/unbuttoning
Proximal lower limb—pelvic/thigh: Cannot rise from chair or squatting position, waddling gait
Distal upper limbs—leg/foot: Difficulty in gripping chappals, cannot walk on heels/toes foot drop
Neck muscles Dropped head/broken neck
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Trunk Inability to roll on the bed
Example
Guillain–Barré syndrome (GBS): History of preceding gastrointestinal (GI) infection followed by
acute onset difficulty in getting up from squatting position, difficulty walking, progressing to involve
upper limbs (difficulty combing hair), and neck muscle weakness. No sensory symptoms.
Wasting/Loss of Muscle Bulk
Wasting—present/absent
Fasciculations—present/absent
Stiffness of Limbs
Stiffness—present/absent
Heaviness—present/absent
Gait Abnormalities
Limp or dragging foot
Scissoring/circumduction.
Involuntary Movements
Type
Symmetrical/asymmetrical
Part of the body involved
Present at rest
Functional disability.
SENSORY DYSFUNCTION
Numbness/loss of feeling
Altered feeling:
Paresthesia
Dysesthesias (tingling and pin-needles)
Spontaneous pain
Pattern of sensory loss.
CEREBELLAR HISTORY
Swaying to one side
Tremors while reaching objects
Lack of coordination of activities
Overshooting acts
Abnormal involuntary eye movements (oscillopsia/nystagmus).
HISTORY SUGGESTING MENINGITIS/RAISED INTRACRANIAL
PRESSURE
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Headache
Neck pain
Projectile vomiting
Blurring of vision
Seizures
Photophobia.
HISTORY SUGGESTING AUTONOMIC DYSFUNCTION
Dryness of skin
Palpitations
Perspiration
Syncopal attacks/postural giddiness
Bladder dysfunction:
Urinary retention
Loss of awareness of bladder control
Frequency, urgency
Urge/overflow incontenence.
REVIEW OF COMMON NEUROLOGICAL SYMPTOMS
Headaches
Onset and duration of headache
Location of headache, unilateral versus bilateral
Severity
Frequency
Radiation
Quality of headache (dull and diffuse)
Types:
Continuous
Pulsating
Stabbing
Sharp
Throbbing
Dull
Thunderclap
Alleviating factors
Triggers for the headache/aggravating factors
Temporal association (headache not worse in mornings)
Association with nausea/vomiting/tearing of eyes/redness of eyes
Vision changes before or during headache
Precipitating factors:
Stress
Menses
Allergens
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Sleep deprivation
Coughing
Straining
Bending forwards
Associated motor/sensory symptoms: Weakness, numbness, and tingling in upper or lower
extremities
Photophobia/phonophobia
Systemic symptoms—weight loss, low energy, and anorexia
Fever and neck stiffness
History of head trauma
History of migraine
Family history of migraines
Effect on daily activities
Use of oral contraceptive pills
Caffeine intake
Smoking and alcohol history.
Example
Classical migraine: Visual aura followed by insidious onset, unilateral, severe pulsating type of
heading lasting for >4 hours associated with nausea and photophobia. Repeated such attacks
every month with history of some identifiable precipitating factors and a positive family history of
migraine.
Seizures
Onset and duration
Frequency
Factors which precipitate these episodes
Injury sustained as a result of the seizure
Postictal symptoms: Confusion
Associated sensory deficits
Associated motor deficits
Associated cognitive deficits
Muscle spasms
Anatomical progression of motor involvement (e.g. Jacksonian March)
Symptoms suggesting aura
Associated incontinence
Tongue biting and salivation
Automatisms associated with these episodes
History of head trauma
Perinatal infection
Drug history
History of seizure disorder
Family history of seizure disorders
Effect on daily activities.
Example
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Generalized tonic clonic seizure (GTCS): Abrupt onset tonic clonic contraction of muscle associated
with tongue bite and urinary incontinence. Patients generally regain consciousness within few
minutes with postictal confusion and headache.
Past history:
Asthma
Chronic obstructive airway disease
Tuberculosis
History of contact with tuberculosis
Diabetes mellitus (DM)
Hypertension (HTN)
Ischemic heart disease (IHD)
Seizure disorder and drugs used (in detail).
Family history:
(draw pedigree chart representing three generations)
Personal history:
Bowel habits
Bladder habits
Appetite
Loss of weight
Occupational exposure
Sleep
Dietary habits and taboo
Food allergies
Smoking (in smoking Index or Pack years)
Alcohol history (__ grams of alcohol/day or ___ units of alcohol/week).
Menstrual and obstetric history:
G__P__L__A__
Age of menarche __
Menopause at __
Flow—amenorrhea/oligorrhea/menorrhagia.
Summarize:
Differential diagnosis:
GENERAL EXAMINATION
Patient
Conscious
Cooperative
Obeying commands
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Body Mass Index (BMI)
Wt (kg)/Ht2
(meters)
Grading according to WHO for Southeast Asian countries
Vitals
Pulse
Rate
Rhythm
Volume
Character
Vessel wall thickening
Radio-radial delay and radio-femoral delay
Peripheral pulses
Carotid and vertebral bruit
Blood pressure
Right arm
Left arm
Leg—right/left
Respiratory rate
Regular
Abdominothoracic (male) or thoracoabdominal (female)
Usage of accessory muscles
Jugular venous pulse
Waveform
Jugular venous pressure
__ cm of blood above sternal angle (+ 5 cm water)
On Physical Examination
Pallor
Icterus
Cyanosis
Clubbing
Lymphadenopathy
Edema
Others Head to Toe
Nerve thickening
Neurocutaneous markers
External markers of atherosclerosis
Signs of nutritional deficiency, alcoholism, etc.
Any other general examination finding
NERVOUS SYSTEM EXAMINATION
Right/left handed person
Education
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