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Regain Control Over Movement

Expert care for Parkinson's, tremor, dystonia with tailored therapies and functional focus

Book Movement Disorder Consultation
80%
Motor Improvement
With optimized levodopa therapy and adjuncts
3-5 years
Honeymoon Period
Excellent symptom control with initial therapy
65%
Tremor Reduction
With botulinum toxin in select cases

When to Consult

  • Resting tremor (shaking when hand is relaxed)
  • Slowness of movement (bradykinesia) or stiffness
  • Balance problems or shuffling gait
  • Changes in handwriting (micrographia)
  • Loss of facial expression or soft voice
  • Dystonia, chorea, or abnormal involuntary movements

Understanding Parkinson's Disease in the Indian Context

Parkinson's Disease (PD)—a progressive neurodegenerative disorder causing tremor, stiffness, slowness, and balance problems—affects 1 in 500 Indians over 65. At Ajuda Hospitals, our Movement Disorder Clinic combines medication optimization, botulinum toxin therapy, and multidisciplinary rehabilitation to maximize function and independence.

PD results from dopamine-producing neuron loss in the substantia nigra. Symptoms emerge when 60-80% of dopamine is depleted. While incurable, treatment with levodopa and adjuncts provides excellent symptom control for years—the "honeymoon period." As disease advances, motor fluctuations and non-motor symptoms (dementia, psychosis) require complex management.

Indian patients face unique challenges: delayed diagnosis (tremor attributed to "old age"), limited access to physiotherapy in rural areas, and caregiver burden on joint families. We address these with telemedicine follow-up, home exercise programs, and caregiver education in Telugu, Hindi, Urdu, and English.

When to Consult Our Movement Disorder Specialists

⚠️ Consult If You Experience:

  • ✓ Resting tremor (shaking when hand relaxed)
  • ✓ Slowness of movement or stiffness
  • ✓ Balance problems, shuffling gait, or frequent falls
  • ✓ Handwriting getting smaller (micrographia)

Early diagnosis and treatment improve quality of life. Don't dismiss symptoms as "normal aging"—Parkinson's is treatable.

Our Diagnostic Approach

Clinical Diagnosis

UK Brain Bank Criteria: Bradykinesia (slowness) PLUS one of:

  • Rest Tremor: 4-6 Hz, worse at rest, improves with action (e.g., pill-rolling).
  • Rigidity: Increased muscle tone, "cogwheel" resistance to passive movement.
  • Postural Instability: Impaired balance, falls (late feature).

Supporting Features: Asymmetric onset, response to levodopa, anosmia (loss of smell), REM sleep behavior disorder.

Differential Diagnosis

Rule out mimics:

  • Essential Tremor: Action tremor (not rest), family history, alcohol-responsive.
  • Atypical Parkinsonism: MSA (autonomic failure, cerebellar signs), PSP (falls, vertical gaze palsy), CBD (alien limb).
  • Drug-Induced: Antipsychotics (haloperidol), metoclopramide, valproate—reversible if stopped.
  • Vascular Parkinsonism: Lower-body predominant, MRI shows subcortical infarcts.

Neuroimaging

MRI Brain: Exclude stroke, tumor, hydrocephalus. Normal in PD (diagnosis is clinical). DaTscan: SPECT imaging of dopamine transporters; abnormal in PD vs essential tremor. Used when diagnosis uncertain.

Functional Assessment

UPDRS (Unified Parkinson's Disease Rating Scale): Quantifies motor and non-motor symptoms (0-199; higher = worse). Hoehn & Yahr Staging: 1 (unilateral) to 5 (wheelchair-bound). Falls Assessment: Timed Up-and-Go test; home safety evaluation by OT.

Treatment Pathways

Levodopa/Carbidopa Therapy

Gold Standard: Levodopa crosses blood-brain barrier, converts to dopamine. Carbidopa blocks peripheral conversion (reduces nausea).

Dosing: Start 100/25mg tid; titrate to symptom control (max ~1000mg levodopa/day). Take 30 min before meals (protein competes for absorption).

Response: 80-90% motor improvement in early disease. If no response, reconsider diagnosis.

Side Effects: Nausea (dose with domperidone initially), orthostatic hypotension, dyskinesia (late).

Dopamine Agonists

Options: Pramipexole, ropinirole stimulate dopamine receptors directly (don't require conversion).

Use: Younger patients (<65) to delay levodopa (postpone motor fluctuations). Monotherapy or levodopa adjunct.

Side Effects: Impulse control disorders (gambling, hypersexuality, compulsive shopping), daytime sleepiness, hallucinations (especially elderly), leg edema.

Monitoring: Screen for ICDs at every visit; reduce/stop if emerge.

MAO-B Inhibitors

Options: Rasagiline 1mg daily, selegiline 5mg bid. Mechanism: Block MAO-B enzyme that breaks down dopamine; extends duration. Benefit: Modest motor improvement; may delay levodopa need by months. Side Effects: Insomnia (take morning), orthostatic hypotension.

COMT Inhibitors

Entacapone 200mg with each levodopa dose; blocks peripheral dopamine breakdown, extends half-life. Use: When "wearing off" (symptoms return before next dose). Adds 1-2 hours ON time per dose. Side Effect: Orange urine (harmless), diarrhea (transient).

Amantadine

Dual Use: Mild anti-parkinsonian effect early; reduces dyskinesia later. Dose: 100mg bid-tid. Side Effects: Livedo reticularis (skin mottling), ankle edema, confusion (elderly).

Botulinum Toxin Injections

Indications:

  • Cervical Dystonia: Involuntary neck turning/tilting.
  • Blepharospasm: Involuntary eyelid closure.
  • Limb Dystonia: Foot inversion, hand cramping.
  • Sialorrhea: Drooling (inject parotid/submandibular glands).
  • Tremor: Focal tremor (head, hand) unresponsive to meds.

Procedure: Inject overactive muscles; lasts 3-4 months. Repeat as needed.

Outcomes: 60-70% improvement in targeted symptom.

Physical & Occupational Therapy

Goals: Maintain mobility, prevent falls, preserve independence.

Interventions:

  • Gait Training: Large-step practice, obstacle courses, dual-task training.
  • Balance Exercises: Tai chi, tandem walking, perturbation training.
  • LSVT LOUD: Voice therapy—increase volume to overcome hypophonia.
  • LSVT BIG: Movement amplitude training—counteract small movements.
  • ADL Strategies: Adaptive utensils, grab bars, shower chairs.

Dose: Intensive 4-8 weeks (3-5 sessions/week), then home maintenance program.

Speech & Swallow Therapy

For: Hypophonia (soft voice), dysarthria (slurred speech), dysphagia (swallowing difficulty—aspiration risk). Techniques: Lee Silverman Voice Treatment, chin-tuck swallow, diet modifications (thickened liquids).

What to Expect: Your Care Journey

First Visit (60 min)

History (onset, progression, symptoms), neurological exam (tremor, rigidity, bradykinesia, gait), UPDRS scoring. Start levodopa if diagnosis clear.

Week Follow-Up

Assess treatment response. If good improvement → confirm PD diagnosis. Titrate levodopa to optimal dose (balance efficacy vs side effects).

Month Visits

Monitor for motor fluctuations (wearing off, dyskinesia), non-motor symptoms (sleep, mood, cognition). Adjust medications; add COMT inhibitor or agonist if needed.

Annual Reviews

UPDRS scoring to track progression. Screen for dementia (MoCA test), depression (PHQ-9), orthostatic hypotension. Update PT/OT prescriptions. Discuss advanced therapies if severe fluctuations.

Advanced Disease (10+ years)

Complex regimen (5-6 drugs); consider DBS if severe OFF time/dyskinesia. Manage psychosis (quetiapine, pimavanserin), dementia (rivastigmine), dysautonomia (midodrine for BP). Caregiver respite planning.

Technology & Innovation

Levodopa-Carbidopa Intestinal Gel (LCIG)

For advanced PD with severe motor fluctuations unresponsive to oral therapy. Continuous levodopa infusion via PEG-J tube connected to portable pump.

Benefits: Stable dopamine levels; fewer OFF periods; reduced dyskinesia. Drawbacks: Surgical tube placement, device care, high cost (insurance authorization required).

Deep Brain Stimulation (DBS)

Candidates: Good levodopa response but intolerable fluctuations/dyskinesia; age <70; no significant dementia. Procedure: Electrodes implanted in subthalamic nucleus (STN) or globus pallidus interna (GPi); connected to battery in chest. Outcomes: 4-6 hour ON time increase; 50% dyskinesia reduction; 30-50% medication reduction. Risks: Surgical (hemorrhage 1-2%), hardware infection, speech/gait worsening (STN), battery replacement every 3-5 years.

Our neurosurgery team coordinates pre-operative evaluation (cognitive testing, MRI) and post-op programming.

Telemedicine Movement Disorder Clinic

  • Monthly video consults for medication titration.
  • Caregiver-assisted motor assessments via smartphone (UPDRS finger taps, gait).
  • Remote adjustment of DBS settings (if implanted).
  • Quarterly in-person visits for detailed exam and therapy renewals.

Preventing Complications

Falls: Leading cause of hospitalization in PD. Prevention: balance training, home modifications (remove rugs, install grab bars), walking aids, hip protectors.

Dementia: 30-40% develop PD dementia. Risk factors: older age, hallucinations, postural instability. Treatment: rivastigmine (cholinesterase inhibitor); avoid anticholinergics (worsen cognition).

Psychosis: Hallucinations (usually visual—"people/animals in room"), delusions (paranoia). Triggered by dopaminergic meds. Management: reduce agonists, quetiapine 25mg hs, pimavanserin if severe.

Aspiration Pneumonia: Dysphagia → food/liquid entering airway. Prevention: swallow evaluation, diet modifications, upright positioning during meals.

Orthostatic Hypotension: BP drop on standing → dizziness, falls. Management: salt, fluids, compression stockings, midodrine, fludrocortisone.

Why Ajuda for Movement Disorder Care?

💊 Medication Expertise

Fine-tuned levodopa regimens, rational combinations, management of fluctuations and dyskinesia.

💉 Botulinum Toxin

For dystonia, tremor, drooling—targeted relief where meds fall short.

🏥 Multidisciplinary

Neurology, PT, OT, speech, psychiatry—coordinated care for motor and non-motor symptoms.

Take the First Step

If new symptoms: Call 9010550550 for diagnostic evaluation. Early treatment improves quality of life.

If on medications but struggling: Request medication optimization visit. Fluctuations and dyskinesia are manageable with adjustments.

If advanced disease: Discuss LCIG or DBS candidacy. Advanced therapies restore function when meds alone are insufficient.

Ajuda Hospitals: Where movement disorders meet precision medicine, and every good day counts.

Diagnosis Approach

1

Clinical Diagnosis

History and exam per UK Brain Bank criteria: bradykinesia plus rest tremor, rigidity, or postural instability. Response to levodopa confirms diagnosis.

2

Differential Diagnosis

Rule out atypical parkinsonism (MSA, PSP, CBD), drug-induced (antipsychotics, metoclopramide), vascular, essential tremor.

3

Neuroimaging

MRI brain to exclude structural causes (stroke, tumor, hydrocephalus). DaTscan (dopamine transporter imaging) if diagnosis unclear.

4

Functional Assessment

UPDRS scoring (Unified Parkinson's Disease Rating Scale) for motor and non-motor symptoms; H&Y staging; assess falls, freezing, dyskinesia.

Treatment Options

Levodopa/Carbidopa Therapy

Gold standard: replaces dopamine; start 100/25mg tid, titrate to symptom control. Avoid protein-rich meals (competes for absorption).

80-90% motor improvement in early disease
Lifelong; dose adjustments as disease progresses

Dopamine Agonists

Pramipexole, ropinirole for younger patients (&lt;65) to delay levodopa (postpone motor fluctuations). Side effects: impulse control disorders, hallucinations.

Moderate benefit; adjunct to levodopa
Years; may need to reduce/stop if side effects

MAO-B Inhibitors

Rasagiline, selegiline block dopamine breakdown; mild symptomatic benefit; possible neuroprotection (unproven).

Modest motor benefit; delays levodopa need
Long-term adjunct therapy

COMT Inhibitors

Entacapone extends levodopa half-life; reduces 'wearing off' (end-of-dose motor decline). Use when motor fluctuations emerge.

Adds 1-2 hours ON time per dose
Combined with each levodopa dose

Botulinum Toxin Injections

For focal dystonia (cervical, blepharospasm), tremor, sialorrhea (drooling). Injected into overactive muscles; lasts 3-4 months.

60-70% improvement in focal symptoms
Repeated every 12-16 weeks

Physical & Occupational Therapy

Gait training, balance exercises, home safety modifications, ADL strategies (buttoning, eating). LSVT LOUD for voice, LSVT BIG for movement amplitude.

Improves mobility and reduces falls
Intensive 4-8 weeks, then maintenance

Expected Outcomes

Treatment Timeline

0-5 Years (Honeymoon)

Excellent response to levodopa; minimal side effects

5-10 Years

Motor fluctuations ('wearing off', dyskinesia) emerge; complex regimen needed

10-15 Years

Non-motor symptoms (dementia, psychosis, dysautonomia); caregiver support critical

15+ Years

Advanced disease; consider DBS if motor complications severe

Success Metrics

  • Maintained independence in ADLs for 10+ years
  • Reduced falls and hospitalization with therapy optimization
  • Quality of life preserved with multidisciplinary support