Lithium and Neuroleptics in Combination: Is There Enhancement of Neurotoxicity Leading to Permanent Sequelae?
- 1 October 1996
- journal article
- research article
- Published by Wiley in The Journal of Clinical Pharmacology
- Vol. 36 (10) , 951-962
- https://doi.org/10.1002/j.1552-4604.1996.tb04763.x
Abstract
Neurotoxicity in relation to concomitant administration of lithium and neuroleptic drugs, particularly haloperidol, has been an ongoing issue. This study examined whether use of lithium with neuroleptic drugs enhances neurotoxicity leading to permanent sequelae. The Spontaneous Reporting System database of the United States Food and Drug Administration and extant literature were reviewed for spectrum cases of lithium/neuroleptic neurotoxicity. Groups taking lithium alone (Li), lithium/haloperidol (LiHal) and lithium/ nonhaloperidol neuroleptics (LiNeuro), each paired for recovery and sequelae, were established for 237 cases. Statistical analyses included pairwise comparisons of lithium levels using the Wilcoxon Rank Sum procedure and logistic regression to analyze the relationship between independent variables and development of sequelae. The Li and Li-Neuro groups showed significant statistical differences in median lithium levels between recovery and sequelae pairs, whereas the LiHal pair did not differ significantly. Lithium level was associated with sequelae development overall and within the Li and LiNeuro groups; no such association was evident in the LiHal group. On multivariable logistic regression analysis, lithium level and taking lithium/haloperidol were significant factors in the development of sequelae, with multiple possibly confounding factors (e.g., age, sex) not statistically significant. Multivariable logistic regression analyses with neuroleptic dose as five discrete dose ranges or actual dose did not show an association between development of sequelae and dose. Database limitations notwithstanding, the lack of apparent impact of serum lithium level on the development of sequelae in patients treated with haloperidol contrasts notably with results in the Li and LiNeuro groups. These findings may suggest a possible effect of pharmacodynamic factors in lithium/neuroleptic combination therapy.Keywords
This publication has 61 references indexed in Scilit:
- Clinical Pharmacokinetics of LithiumThe Journal of Clinical Pharmacology, 1994
- LithiumDrugs, 1993
- Long-term biphasic effects of lithium treatment on phospholipase C-coupled m3-muscarinic acetylcholine receptors in cultured cerebellar granule cellsNeurochemistry International, 1993
- An autopsy case of cerebellar degeneration following lithium intoxication with neuroleptic malignant syndromeActa Pathologica Japonica, 1993
- Regional distribution and kinetics of haloperidol binding in human brain: A pet study with [18F]haloperidolSynapse, 1992
- Comparison of Standard and Low Serum Levels of Lithium for Maintenance Treatment of Bipolar DisorderNew England Journal of Medicine, 1989
- The Bioavailability and Pharmacokinetics of Oral and Depot Intramuscular Haloperidol in Schizophrenic PatientsThe Journal of Clinical Pharmacology, 1987
- Neuroleptic Malignant SyndromeNew England Journal of Medicine, 1985
- Drug Prescribing Pattern of a Psychiatric University Hospital in GermanyPharmacopsychiatry, 1983
- The substituted benzamides - a novel class of dopamine antagonistsLife Sciences, 1979