Hemiplegia
Paralysis of one half (right or left) of the body.
Commonly occurs after cerebro-vascular accidents (stroke) or traumatic brain injury (TBI).
Paraplegia
Paralysis of the lower half of the body (both legs ± lower trunk).
Typical aetiologies: spinal cord injury (SCI) below T\,1, congenital defects (spina bifida), tumours, vascular lesions.
Quadriplegia / Tetraplegia
Paralysis from the neck downward: trunk + both upper & lower limbs.
Occurs with cervical cord damage above C\,6, high cervical tumours, or advanced neuro-degenerative disease.
Myasthenia Gravis (MG)
Chronic auto-immune disease; antibodies destroy post-synaptic acetyl-choline receptors → failed neuromuscular transmission.
Hallmarks: fluctuating skeletal-muscle weakness (ocular, bulbar, limb).
Tensilon (edrophonium) test & anti-AChR antibodies diagnostic.
Guillain-Barré Syndrome (GBS)
Acute post-infectious poly-neuropathy; immune attack on peripheral-nerve myelin.
Ascending symmetrical weakness → areflexia; watch for respiratory failure.
Parkinson’s Disease (PD)
Age-related, progressive loss of dopamine-producing cells in substantia nigra.
“Cardinal” triad: bradykinesia, resting tremor, postural instability.
Alzheimer’s Disease (AD)
Irreversible cortical atrophy with β-amyloid plaques + tau tangles.
Slow decline in memory → executive dysfunction → loss of ADL skills.
Late-onset: >65 y; Early-onset: 30–60 y (rare).
Bell’s Palsy
Acute unilateral facial-nerve (VII) paralysis of unknown cause (likely viral inflammation).
S/S: ptosis, mouth droop, salivation, corneal drying.
Usually self-resolving; early corticosteroids ↓ severity; eye protection imperative.
Non-modifiable:
Ageing; genetic predisposition.
Modifiable:
Hypertension, atherosclerosis, diabetes, gout, obesity, smoking, stress, poor diet, adverse environment.
Evaluates best Eye (E), Verbal (V), Motor (M) responses to stimuli.
Score range: 3\;\text{(deep coma)} \rightarrow 15\;\text{(fully alert)}.
Eye (E) \max 4: spontaneous 4 | to speech 3 | to pain 2 | none 1.
Verbal (V) \max 5: oriented 5 | confused 4 | inappropriate words 3 | incomprehensible sounds 2 | none 1.
Motor (M) \max 6: obeys commands 6 | localises pain 5 | withdraws 4 | abnormal flexion (decorticate) 3 | extension (decerebrate) 2 | none 1.
Serial charting identifies deterioration/improvement trends.
Airway/Breathing
Lateral position, head–neck alignment, oral airway, bedside suction, O₂ or mechanical ventilation PRN.
Circulation/Nutrition/Fluids
Enteral or IV feeding; strict I&O; monitor electrolytes, CVP/PA pressures; prevent dehydration or overload.
Bowel & Bladder
Record stool/urine; prevent constipation (hydration, mild laxative, suppository); catheter care/Paul’s tubing; weigh diapers.
Comfort & Pain
Reposition q2h; support limbs; observe subtle pain cues; give analgesics.
Temperature Regulation
Axillary/rectal probes; address hyper/hypothermia; avoid oral thermometers.
Immobility Complications
Pressure-area care, passive ROM, anti-embolism stockings, prophylactic anticoagulants.
Infection Control
Aseptic technique; monitor VS/q4h; early antibiotics if indicated.
Self-care & Hygiene
Daily bed-bath, oral/eye care (lubricants), hair/nails, dryness to prevent sores.
Psychosocial
Assume hearing intact; speak respectfully, orient to time/time, encourage family interaction, provide sensory input (radio/TV).
Definition: Infection/inflammation of meninges.
Causes: Mainly CSF invasion by bacteria (e.g., Neisseria meningitidis, H. influenzae) or viruses; also non-infective.
Pathophysiology: Inflamed meninges → exudate ↑ ICP; ↑ CSF production; cerebral irritation → convulsions; scarring → epilepsy/hydrocephalus.
Clinical Manifestations: Flu-like prodrome, high fever, headache, photophobia, neck stiffness, positive Brudzinski/Kernig, altered LOC, convulsions, focal signs.
Diagnostics: Lumbar puncture → cloudy CSF, ↑ WBC, ↑ protein, ↑ pressure.
Complications: Septic shock, petechiae, Waterhouse–Friderichsen (adrenal failure), septic arthritis (H. influenzae).
Medical Tx: IV antibiotics/acyclovir; anticonvulsants; prophylaxis for contacts (meningococcal).
Nursing: Neuro obs, temp control (tepid sponge, paracetamol), quiet room, analgesia (DF-118 if severe), isolation as per policy.
Health Ed: Vaccination, early treatment, contact prophylaxis.
Definition: Inflammation of brain parenchyma.
Causes: Mostly viral; epidemic (mosquito/tick); post-viral.
Manifestations: Gradual onset headache, fever, lethargy, ↓ LOC, seizures.
Management: Supportive (ABC, nutrition), prevent immobility issues, monitor neuro changes; antivirals (acyclovir/vidarabine) esp. HSV before coma.
Definition: Chronic disorder with recurrent, spontaneous, idiopathic seizures.
Causes: 75\% idiopathic; known triggers: trauma, congenital CNS defects, metabolic errors, infections, tumours, vascular lesions, electrolyte/acid-base imbalances.
Pathophysiology: Hyper-synchronous neuronal discharge from seizure focus; may generalise.
Types:
Petit mal (absence): brief blank stare/twitch; no fall.
Grand mal (tonic–clonic): aura → tonic stiffening → clonic jerks → post-ictal sleep; possible incontinence, injury.
Partial: simple (Jacksonian) – focal motor without LOC; complex – focal + impaired consciousness.
Diagnostics: EEG patterns.
Treatment:
Pharmacological: Anticonvulsants suppress discharge or spread (e.g., phenytoin, carbamazepine, valproate).
Refractory cases: cortical resection, stereotactic ablation, vagal stimulation, biofeedback.
Status epilepticus: emergency—secure ABC, IV benzodiazepine/phenytoin; if refractory → phenobarbitone infusion → GA with ventilation & continuous EEG.
Nursing During Seizure: Side-lying, protect airway, do not force mouth open, note duration & features, document.
Health Education: Lifelong meds compliance, Medic-Alert, avoid triggers (ETOH, stress, sleeplessness), safe recreation (no solo swimming/climbing), driving allowed after \ge 2 y seizure-free.
Assessment Mnemonic — PQRSTU
P – Precipitating/Palliating.
Q – Quality (burning, stabbing…).
R – Radiation.
S – Severity (scale 0\text{–}10).
T – Timing (onset, duration).
U – Understanding (patient’s perspective).
Observation of Non-Verbal Cues: posture, facial grimace, agitation, sounds; critical for children, elderly, unconscious, cognitively-impaired.
Age-/Cognition-Specific Tools:
Faces scale; Oucher 0\text{–}10 photos; Colour tool; FLACC (Face, Legs, Activity, Cry, Consolability).
Principles of Management:
Comprehensive assessment; believe patient; separate & rate each pain; integrate pharmacologic & non-pharmacologic measures; adjust for acute vs chronic goals (elimination vs minimisation/rehabilitation).
Non-Pharma Options: psychosocial support, physiotherapy, heat/cold, acupuncture, TENS, trigger-point injections, relaxation/distraction, reflexology, aromatherapy, palliative radiotherapy, nerve blocks, surgery & mobility aids.
Education: Provide realistic information, dispel myths, involve family, supply written material, plan for breakthrough pain (e.g., when starting morphine).