Department of Toxicology, Bab-El-Oued Hospital, Avenue Mohamed Lamine Debaghine, 16009 Algiers, Algeria; National Center of Toxicology, Avenue petit Staouali Delly Brahim, 16062 Algiers, Algeria.
Department of Biology and Toxicology, Ait-Idir Hospital, Avenue Abderrezak Hahad Casbah, 16017 Algiers, Algeria.
Toxicol Appl Pharmacol. 2018 Aug 1;352:1-8. doi: 10.1016/j.taap.2018.05.015. Epub 2018 May 17.
Antipsychotic drugs are known to induce neuromuscular effects. In this study, we review 13 years (2002-2014) of antipsychotic intoxications reported by the anti-poisoning center of Algiers (APCA). The most recorded symptoms were neuromuscular/muscular disorders, of which haloperidol was the most inducer among all antipsychotics. A prospective study was conducted between December 2012 and January 2017 to evaluate muscle effects generated after intentional or accidental ingestion of haloperidol. Fifty-one patients admitted in different emergency departments in Algiers were included in this study. Urine and blood samples were collected from each patient for biological and toxicological monitoring and a group of healthy volunteers was assessed for comparison purpose. There was no significant difference in plasma lactate dehydrogenase (LDH) activity between healthy volunteers and exposed patients even when high levels of haloperidol were recorded. In contrast, selenium concentration and creatine kinase (CK) activity in plasma samples were significantly higher in patients exposed to high levels of haloperidol compared to healthy volunteers. Large percentage of patients exposed to high levels of haloperidol presented a significant elevated CK activity and high selenium concentration regarding the physiological thresholds. Additionally, CK activity and selenium concentration correlated positively with plasma content of haloperidol suggesting a dose-dependent relationship. In conclusion, some biomarkers (CK and selenium) may reflect muscle adverse effects of high haloperidol exposure that result possibly from muscle rigidity.
抗精神病药物已知可引起神经肌肉效应。在这项研究中,我们回顾了 2002 年至 2014 年期间,由阿尔及尔中毒控制中心(APCA)报告的 13 年抗精神病药物中毒病例。记录最多的症状是神经肌肉/肌肉疾病,其中氟哌啶醇是所有抗精神病药物中最主要的诱导剂。2012 年 12 月至 2017 年 1 月期间进行了一项前瞻性研究,以评估故意或意外摄入氟哌啶醇后产生的肌肉效应。本研究纳入了阿尔及尔不同急诊科收治的 51 名患者。从每位患者采集尿液和血液样本进行生物和毒理学监测,并评估了一组健康志愿者作为对照组。即使记录到高水平的氟哌啶醇,健康志愿者和暴露患者的血浆乳酸脱氢酶(LDH)活性也没有显著差异。相比之下,暴露于高水平氟哌啶醇的患者的血浆硒浓度和肌酸激酶(CK)活性明显高于健康志愿者。大量暴露于高水平氟哌啶醇的患者的 CK 活性和硒浓度显著升高,超出了生理阈值。此外,CK 活性和硒浓度与血浆中氟哌啶醇含量呈正相关,提示存在剂量依赖性关系。总之,一些生物标志物(CK 和硒)可能反映了高水平氟哌啶醇暴露引起的肌肉不良反应,这可能是由肌肉僵硬引起的。