Effect of Antipsychotic Type and Dose Changes on Tardive Dyskinesia and Parkinsonism Severity in Patients With a Serious Mental Illness

Autor: Hans W. Hoek, P. Roberto Bakker, Peter N. van Harten, Glenn E. Matroos, Jim van Os, Marina A. J. Tijssen, Marjan Drukker, Charlotte L. Mentzel
Přispěvatelé: Movement Disorder (MD), Promovendi MHN, Psychiatrie & Neuropsychologie, RS: MHeNs - R2 - Mental Health, MUMC+: Hersen en Zenuw Centrum (3), MUMC+: MA Psychiatrie (3), RS: CAPHRI other
Rok vydání: 2017
Předmět:
Adult
Male
medicine.medical_specialty
Movement disorders
medicine.medical_treatment
Dopamine Agents
Tardive dyskinesia
03 medical and health sciences
0302 clinical medicine
QUALITY-OF-LIFE
Internal medicine
CATIE SCHIZOPHRENIA TRIAL
medicine
Humans
Tardive Dyskinesia
OUTPATIENT HEALTH OUTCOMES
DRUGS
Parkinson Disease
Secondary

Netherlands Antilles
Psychiatry
Prospective cohort study
Antipsychotic
METAANALYSIS
Neurologic Examination
Polypharmacy
Drug Substitution
ATYPICAL ANTIPSYCHOTICS
business.industry
Mental Disorders
Parkinsonism
Middle Aged
INDUCED MOVEMENT-DISORDERS
medicine.disease
PREVALENCE
030227 psychiatry
Psychiatry and Mental health
Cross-Sectional Studies
Treatment Outcome
Tolerability
TOLERABILITY
Female
Guideline Adherence
POLYPHARMACY
Abnormal Involuntary Movement Scale
medicine.symptom
business
030217 neurology & neurosurgery
Antipsychotic Agents
Zdroj: Journal of Clinical Psychiatry, 78(3), E279-E285. Physicians Postgraduate Press Inc.
ISSN: 0160-6689
DOI: 10.4088/jcp.16m11049
Popis: OBJECTIVE To test the efficacy of current treatment recommendations for parkinsonism and tardive dyskinesia (TD) severity in patients with severe mental illness (SMI). METHODS We present an 18-year prospective study including all 223 patients with SMI (as defined by the 1987 US National Institute of Mental Health, which were based on DSM-III-R diagnostic criteria) receiving care from the only psychiatric hospital of the former Netherlands Antilles. Eight clinical assessments (1992-2009) focused on movement disorders and medication use. Tardive dyskinesia was measured by the Abnormal Involuntary Movement Scale and parkinsonism by the Unified Parkinson's Disease Rating Scale. Antipsychotics were classified into first-generation antipsychotic (FGA) versus second-generation antipsychotic (SGA) and high versus low dopamine 2 (D₂) affinity categories. The effect that switching has within each category on subsequent movement scores was calculated separately by using time-lagged multilevel logistic regression models. RESULTS There was a significant association between reduction in TD severity and starting/switching to an FGA (B = -3.54, P < .001) and starting/switching to a high D₂ affinity antipsychotic (B = -2.49, P < .01). Adding an SGA to existing FGA treatment was associated with reduction in TD severity (B = -2.43, P < .01). For parkinsonism, stopping antipsychotics predicted symptom reduction (B = -7.76, P < .01 in FGA/SGA-switch model; B = -7.74, P < .01 in D₂ affinity switch model), while starting a high D₂ affinity antipsychotic predicted an increase in symptoms (B = 3.29, P < .05 in D₂ affinity switch model). CONCLUSIONS The results show that switching from an FGA to an SGA does not necessarily result in a reduction of TD or parkinsonism. Only stopping all antipsychotics reduces the severity of parkinsonism, and starting an FGA or a high D₂ affinity antipsychotic may reduce the severity of TD.
Databáze: OpenAIRE