Literature DB >> 22035899

Amisulpride and neuroleptic malignant syndrome.

Ming-Che Tu1, Cheng-Cheng Hsiao.   

Abstract

Neuroleptic malignant syndrome (NMS) is a rare but lethal complication of neuroleptics. Its incidence ranges between 0.02% and 3%. Amisulpride, a second generation neuroleptic, was associated with rhabdomyolysis in one report and NMS in 2 reports. Although the precise pathogenesis is still unclear, dopamine receptor blockade is theorized to play a central role. Conventional presentations include hyperthermia, muscle rigidity, and elevated creatine kinase concentrations. However, similar to other second generation neuroleptics, amisulpride induces an atypical form of NMS, which presents with lower degrees of hyperthermia and elevation of creatine kinase than the typical form. This phenomenon makes it difficult to identify early signs of NMS. This study describes the first case of amisulprideinduced NMS in Taiwan, together with a review of the current knowledge on NMS. In this case, the correlation between NMS and amisulpride was categorized as "probable" on the Naranjo adverse drug reaction probability scale.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 22035899

Source DB:  PubMed          Journal:  Chang Gung Med J        ISSN: 2072-0939


  3 in total

Review 1.  [Neuroleptic malignant syndrome].

Authors:  R Knorr; J Schöllkopf; E Haen
Journal:  Nervenarzt       Date:  2018-03       Impact factor: 1.214

2.  Lethal neuroleptic malignant syndrome due to amisulpride.

Authors:  Frank Musshoff; Elke Doberentz; Burkhard Madea
Journal:  Forensic Sci Med Pathol       Date:  2013-03-16       Impact factor: 2.007

Review 3.  Second-generation antipsychotics and neuroleptic malignant syndrome: systematic review and case report analysis.

Authors:  Martino Belvederi Murri; Argentina Guaglianone; Michele Bugliani; Pietro Calcagno; Matteo Respino; Gianluca Serafini; Marco Innamorati; Maurizio Pompili; Mario Amore
Journal:  Drugs R D       Date:  2015-03
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.