Prakash Sanjay, Patel Harsh, Kumar Sunil, Shah Chetsi S
Department of Neurology, Smt. B. K. Shah Medical Institute and Research Centre, Sumandeep Vidyapeeth, Piparia, Waghodia, Vadodara Gujarat, India.
Department of Medicine, Smt. B. K. Shah Medical Institute and Research Centre, Sumandeep Vidyapeeth, Piparia, Waghodia, Vadodara, Gujarat, India.
J Family Med Prim Care. 2024 Apr;13(4):1340-1346. doi: 10.4103/jfmpc.jfmpc_652_23. Epub 2024 Apr 22.
Serotonin syndrome (SS) is an iatrogenic life-threatening condition caused by serotonergic agents. The treatment for SS involves the administration of a serotonin antagonist (cyproheptadine). However, the dosing schedule for cyproheptadine is not uniform in the literature.
We retrospectively evaluated 23 adult patients (>18 years) admitted to the Neurology Department and met the Hunter criteria for SS.
The mean age was 35.2 years, and 52% were female. Ten patients were managed in the intensive care unit (ICU), whereas thirteen patients were admitted to the ward. Hyperreflexia was the most common clinical feature (100%), followed by clonus (91%), tachycardia (83%), and tremor (83%). Other common clinical features were rigidity (65%), increased bowel sound (61%), diaphoresis (48%), fever (43%), hypertension (39%), and myoclonus (30%). All but one patient received two or more serotonergic drugs. Tramadol was the most common serotonergic agent (39%), followed by sodium valproate (21%), and amitriptyline (21%). Cyproheptadine was administered to all patients. All patients admitted in the ICU received a loading dose of 12 mg followed by 2 mg every 2 h for at least 24 h. All patients admitted to the ward were given 4 mg of cyproheptadine three times each day. Every patient showed at least some response to cyproheptadine within 24 h. The total doses of cyproheptadine and the length of treatment differed between patients.
Any response to cyproheptadine at a therapeutic dose within 24 h, even a partial one, could be a diagnostic indicator of the existence of SS.
血清素综合征(SS)是一种由血清素能药物引起的医源性危及生命的病症。SS的治疗包括给予血清素拮抗剂(赛庚啶)。然而,赛庚啶的给药方案在文献中并不统一。
我们回顾性评估了23例入住神经内科且符合SS亨特标准的成年患者(年龄>18岁)。
平均年龄为35.2岁,52%为女性。10例患者在重症监护病房(ICU)接受治疗,13例患者收住普通病房。腱反射亢进是最常见的临床特征(100%),其次是阵挛(91%)、心动过速(83%)和震颤(83%)。其他常见临床特征包括强直(65%)、肠鸣音增强(61%)、多汗(48%)、发热(43%)、高血压(39%)和肌阵挛(30%)。除1例患者外,所有患者均服用了两种或更多血清素能药物。曲马多是最常见的血清素能药物(39%),其次是丙戊酸钠(21%)和阿米替林(21%)。所有患者均接受了赛庚啶治疗。所有入住ICU的患者均给予12mg负荷剂量,随后每2小时给予2mg,至少持续24小时。所有收住普通病房的患者每天给予4mg赛庚啶,分三次服用。每位患者在24小时内对赛庚啶均至少有一定反应。患者之间赛庚啶的总剂量和治疗时间不同。
在24小时内对治疗剂量的赛庚啶有任何反应,即使是部分反应,都可能是SS存在的诊断指标。