Medication-Induced Parkinsonism

Summary about Disease


Medication-induced parkinsonism (MIP) is a syndrome characterized by Parkinson's disease-like symptoms that develop as a side effect of certain medications. It's typically reversible upon discontinuation of the offending drug, although symptoms can persist in some cases. It differs from Parkinson's disease, which is a progressive neurodegenerative disorder.

Symptoms


The symptoms of MIP mirror those of Parkinson's disease and can include:

Tremor (often resting tremor)

Rigidity (stiffness of muscles)

Bradykinesia (slowness of movement)

Postural instability (impaired balance, leading to falls)

Masked face (reduced facial expression)

Shuffling gait

Difficulty initiating movement

Drooling

Soft Speech

Causes


MIP is primarily caused by medications that block or deplete dopamine in the brain. Dopamine is a neurotransmitter crucial for motor control. Common culprit drug classes include:

Antipsychotics: Especially first-generation (typical) antipsychotics like haloperidol, chlorpromazine, and fluphenazine, but also some second-generation (atypical) antipsychotics like risperidone and paliperidone at higher doses.

Anti-nausea medications: Metoclopramide and prochlorperazine.

Certain calcium channel blockers: Flunarizine and cinnarizine.

Some antidepressants: Amoxapine.

Other medications: Tetrabenazine, valproic acid, lithium (rarely)

Is Communicable


No, medication-induced parkinsonism is not communicable. It is a side effect of medication, not an infectious disease.

Precautions


Careful medication review: Healthcare providers should carefully review a patient's medication list, especially in older adults, to identify potential causes of new-onset parkinsonism.

Lowest effective dose: If a potentially causative medication is necessary, it should be prescribed at the lowest effective dose and for the shortest possible duration.

Monitoring: Patients on medications known to cause MIP should be monitored regularly for signs and symptoms of parkinsonism.

Informed consent: Patients should be informed about the potential side effects of medications, including the risk of MIP.

Gradual discontinuation: Discontinuation of the offending medication should be done gradually under medical supervision to avoid withdrawal symptoms or rebound effects.

How long does an outbreak last?


There is no "outbreak" associated with MIP. The duration of symptoms depends on factors such as:

The specific medication and dosage.

The duration of medication use.

Individual patient factors (age, kidney function, etc.).

How quickly the medication is discontinued. Symptoms typically improve within weeks to months after stopping the medication, but in some cases, symptoms may persist longer or even become permanent.

How is it diagnosed?


Diagnosis of MIP typically involves:

Medical history and medication review: A thorough review of the patient's medical history, including all medications they are taking, is crucial.

Neurological examination: To assess for the presence of parkinsonian signs such as tremor, rigidity, bradykinesia, and postural instability.

Ruling out other causes: Other conditions that can cause parkinsonism, such as Parkinson's disease, should be ruled out.

Response to medication discontinuation: Improvement in symptoms after stopping the offending medication is a key diagnostic factor.

DaTscan (Dopamine Transporter Scan): This imaging study can help differentiate between MIP and Parkinson's disease. In Parkinson's disease, the DaTscan usually shows reduced dopamine transporter activity, whereas in MIP, it is often normal.

Timeline of Symptoms


The timeline of symptoms can vary, but generally follows this pattern:

Onset: Symptoms typically develop within weeks to months of starting the offending medication or increasing the dose.

Progression: Symptoms may gradually worsen over time as long as the medication is continued.

Improvement: After stopping the medication, symptoms usually begin to improve within weeks to months.

Resolution: In many cases, symptoms resolve completely after a few months. However, in some individuals, symptoms may persist or only partially improve.

Important Considerations


Differential Diagnosis: It's crucial to differentiate MIP from Parkinson's disease, as the treatment approaches differ.

Older Adults: Older adults are more susceptible to MIP due to age-related changes in dopamine metabolism and increased sensitivity to medications.

Underlying Vulnerability: Some individuals may have an underlying vulnerability to developing parkinsonism, such as a genetic predisposition or subclinical Parkinson's disease.

Tardive Dyskinesia: MIP can sometimes be difficult to distinguish from tardive dyskinesia, another movement disorder caused by antipsychotic medications.

Persistent Symptoms: In rare cases, MIP symptoms may persist even after discontinuing the medication. This can be due to underlying neurodegenerative processes or medication-induced changes in the brain. Consultation with a movement disorder specialist is recommended.