Shin Min Hyeok, Jeong Jin Woo, Yu Tae Yang
Department of Medicine, Division of Endocrinology and Metabolism, Wonkwang University School of Medicine, Iksan, Republic of Korea.
Medicine (Baltimore). 2025 Aug 22;104(34):e44172. doi: 10.1097/MD.0000000000044172.
Clozapine is a unique antipsychotic drug used to treat treatment-resistant psychosis. Clozapine can induce metabolic complications and weight gain, and may lead to acute diabetic complications such as diabetic ketoacidosis (DKA). Neurological side effects of clozapine are relatively rare compared with those of typical antipsychotics; however, several cases have been reported. In particular, reports have suggested that clozapine-induced neuroleptic malignant syndrome (NMS) may present with atypical features. While multiple reports document DKA and NMS occurring separately in patients receiving clozapine, no cases have been reported in which they occur simultaneously. We report a case in which DKA and NMS developed concurrently, with NMS manifesting atypical features and the significant stress associated with NMS hindering recovery from DKA.
A 23-year-old man presented to the emergency department with generalized weakness and shortness of breath. He had been diagnosed with schizophrenia 3 years earlier and was taking medications prescribed at another hospital. His regimen was changed 2 months prior to presentation.
Arterial blood gas analysis revealed high anion gap metabolic acidosis and elevated blood ketone levels. The patient was diagnosed with DKA, and intensive insulin therapy was initiated. However, he developed fever and altered mental status during treatment, and despite intensive insulin therapy, the improvement of metabolic acidosis was hindered. Although the typical symptoms of NMS, such as rigidity and a rapid increase in creatine kinase (CK), were not observed, based on the history of clozapine treatment, persistent fever, altered mental status, and blood pressure instability, NMS was diagnosed.
Insulin and intravenous fluid therapy were continued for DKA, and clozapine was discontinued.
Following clozapine discontinuation, metabolic acidosis, fever, and altered mental status improved rapidly.
DKA and NMS share various signs, such as fever, altered mental status, blood pressure instability, dyspnea, and tachycardia. Therefore, in patients receiving clozapine, the simultaneous occurrence of DKA and NMS should be considered. Additionally, clozapine-induced NMS may present in an atypical form; therefore, even in the absence of typical signs, such as rigidity and a rapid increase in CK, the possibility of NMS should be reconsidered.
氯氮平是一种用于治疗难治性精神病的独特抗精神病药物。氯氮平可引发代谢并发症和体重增加,并可能导致急性糖尿病并发症,如糖尿病酮症酸中毒(DKA)。与典型抗精神病药物相比,氯氮平的神经副作用相对较少;然而,已有数例相关报道。特别是,有报告表明氯氮平诱发的神经阻滞剂恶性综合征(NMS)可能具有非典型特征。虽然多篇报道记录了接受氯氮平治疗的患者分别发生DKA和NMS的情况,但尚未有二者同时发生的病例报道。我们报告了一例DKA和NMS同时发生的病例,其中NMS表现出非典型特征,且与NMS相关的严重应激阻碍了DKA的恢复。
一名23岁男性因全身无力和气促就诊于急诊科。他3年前被诊断为精神分裂症,一直在服用另一家医院开具的药物。在就诊前2个月,他的用药方案发生了改变。
动脉血气分析显示高阴离子间隙代谢性酸中毒和血酮水平升高。患者被诊断为DKA,并开始进行强化胰岛素治疗。然而,他在治疗过程中出现发热和精神状态改变,尽管进行了强化胰岛素治疗,代谢性酸中毒的改善仍受到阻碍。虽然未观察到NMS的典型症状,如僵硬和肌酸激酶(CK)迅速升高,但基于氯氮平治疗史、持续发热、精神状态改变和血压不稳定,诊断为NMS。
继续对DKA进行胰岛素和静脉补液治疗,并停用氯氮平。
停用氯氮平后,代谢性酸中毒、发热和精神状态改变迅速改善。
DKA和NMS有多种共同症状,如发热、精神状态改变、血压不稳定、呼吸困难和心动过速。因此,对于接受氯氮平治疗的患者,应考虑DKA和NMS同时发生的可能性。此外,氯氮平诱发的NMS可能以非典型形式出现;因此,即使没有僵硬和CK迅速升高的典型症状,也应重新考虑NMS的可能性。