What is Tardive Dyskinesia
Tardive dyskinesia (TD) is an involuntary movement disorder typically affecting the orofacial region but potentially involving any body part, associated with long-term use of dopamine receptor-blocking agents (antipsychotics and certain other medications). 1
Clinical Characteristics
TD manifests as abnormal, involuntary, irregular, repetitive movements that are purposeless in nature:
- Orofacial involvement is most common, including involuntary movements of the tongue, face, mouth, or jaw 2
- Limb and truncal movements may occur, often appearing choreoathetotic (writhing, dance-like) in character 2, 3
- Symptoms include facial grimacing, rhythmic tongue protrusion, lip smacking, and involuntary movements of extremities 2
Subtypes and Related Conditions
Beyond classic TD, related tardive syndromes include:
- Tardive dystonia: characterized by slow movements along the body's long axis culminating in spasms, potentially including facial spasms 4
- Tardive akathisia: motor restlessness with feelings of anxiety, agitation, inability to sit still, pacing, and foot tapping 3
Causative Agents
TD develops from exposure to dopamine receptor-blocking medications:
- Antipsychotics (both typical and atypical, though typical agents carry higher risk) are the primary culprits 1
- Metoclopramide carries an FDA black box warning for TD risk, particularly with use exceeding 12 weeks 2
- Other medications with antidopaminergic activity used for nausea or gastrointestinal dysfunction can cause TD with extended use 3
Critical Features
The disorder is often irreversible, making prevention paramount 1, 2:
- TD may persist even after medication discontinuation 1
- The risk of permanence increases with duration of exposure 5
- In some patients, symptoms may lessen or resolve after stopping the offending agent, but there is no guarantee 2
Prevalence and Risk Factors
- Overall prevalence: approximately 20% of neuroleptic-treated patients develop TD 3
- High-risk populations include the elderly (substantially higher rates), women, patients with affective disorders, and those with diabetes 3, 5
- Youth are particularly vulnerable: up to 50% of youth receiving neuroleptics may experience some form of tardive or withdrawal dyskinesia 4, 1
- Total drug exposure is positively correlated with TD risk 3
Diagnostic Criteria
TD diagnosis requires:
- Development during exposure to or withdrawal from neuroleptics 6
- History of neuroleptic use for at least 3 months (or 1 month in patients ≥60 years old) 6
- Presence of characteristic involuntary movements that are out of the patient's control 5
Pathophysiology
While the exact mechanisms remain incompletely understood, altered dopaminergic function likely plays a central role in TD pathogenesis 3, 6.