FDA MEDWATCH REPORT - LITHIUM AND NEUROLEPTICS IN COMBINATION - THE SPECTRUM OF NEUROTOXICITY

Authors
Citation
Sa. Goldman, FDA MEDWATCH REPORT - LITHIUM AND NEUROLEPTICS IN COMBINATION - THE SPECTRUM OF NEUROTOXICITY, Psychopharmacology bulletin, 32(3), 1996, pp. 299-309
Citations number
34
Categorie Soggetti
Psychiatry,Neurosciences,Psychiatry,"Clinical Neurology","Pharmacology & Pharmacy
Journal title
ISSN journal
00485764
Volume
32
Issue
3
Year of publication
1996
Pages
299 - 309
Database
ISI
SICI code
0048-5764(1996)32:3<299:FMR-LA>2.0.ZU;2-Q
Abstract
Classifying neurotoxicity in relation to neuroleptic use has been a lo ngstanding concern with clinical, research, and epidemiologic import. This study examines the clinical manifestations of neurotoxicity and c urrent concepts regarding its classification. The Food and Drug Admins tration (FDA) Spontaneous Reporting System data base and extant litera ture were reviewed for lithium/neuroleptic neurotoxicity spectrum case s. Lithium-alone (Li), lithium/haloperidol (LIHal), and lithium/non-ha loperidol neuroleptics (LiNonHal) groups, each paired for recovery and sequelae, were established for 237 cases. Data on demographic factors , psychiatric diagnosis, and symptoms/signs/findings were tabulated. N euroleptic malignant syndrome (NMS) was used as a paradigm for severe neurotoxicity; the cases were evaluated by two strict, published sets of NMS diagnostic criteria and two ''probable'' classifications (one p ublished and one established for study) based on these criteria. Alter ed consciousness was prominent in all groups. Hypertonia/rigidity was most pronounced in both LiHal groups, possibly reflecting higher relat ive neuroleptic dosing; Li and LiNonHal recovery and sequelae pairs sh owed lower, similar percentages. Among other physical findings, tremor was either most common or prominent, Neither set of strict criteria d iagnosed NMS in more than 30 percent of cases in any group. Expansion of classifications to include ''probable'' diagnoses resulted in appre ciable global group percentage increases for only one set of criteria. The high percentage of study cases not meeting even ''probable'' NMS criteria, despite marked clinical morbidity that at times resulted in permanent sequelae, provides a cautionary note regarding the limitatio ns of formulated diagnostic criteria. Data base caveats notwithstandin g, study findings support the consideration of a spectrum approach to classifying and diagnosing psychotropic-related neurotoxicity.