Department of Pediatrics, Nara Medical University, Kashihara, Nara, Japan.
Brain Dev. 2022 Sep;44(8):546-550. doi: 10.1016/j.braindev.2022.04.005. Epub 2022 Apr 29.
Adrenocorticotropic hormone (ACTH) therapy is a first-line treatment for infantile spasms, which may rarely cause intracranial hemorrhage. However, the changes in blood coagulation during ACTH therapy are poorly understood, with little description in the management guidelines.
To assess the changes in blood coagulation during ACTH therapy.
PATIENTS/METHODS: This retrospective study reviewed the medical records of 10 patients diagnosed with infantile spasms and treated with ACTH therapy, between January 2015 and March 2021. The underlying diseases included intracranial hemorrhage, hypoxic-ischemic encephalopathy, tuberous sclerosis, and cerebral infarction. Antiepileptic drugs administered were valproic acid (VPA), vitamin B6, zonisamide, topiramate, clobazam, clonazepam, and phenobarbital.
The 10 patients had a median age of 8 months (4-17 months) and included eight males. The median fibrinogen (Fbg) level before ACTH therapy was 202 mg/dL (125-392 mg/dL); however, this significantly decreased to 108.5 mg/dL (65-135 mg/dL) during treatment at a median of 12 days after (days 8-17) (p < 0.01). Decreased Fbg levels were observed with and without VPA. This suggests the possible influence of ACTH therapy on Fbg levels, irrespective of the VPA combination. Additionally, prothrombin time and activated partial thromboplastin time were significantly shortened when compared to those before ACTH therapy and at the lowest of Fbg levels.
Careful coagulation monitoring, especially during the second week of treatment, is necessary for the safe completion of ACTH therapy, with or without concomitant VPA.
促肾上腺皮质激素(ACTH)治疗是婴儿痉挛的一线治疗方法,但其可能很少引起颅内出血。然而,ACTH 治疗期间的凝血变化尚不清楚,管理指南中几乎没有描述。
评估 ACTH 治疗期间的凝血变化。
患者/方法:本回顾性研究回顾了 2015 年 1 月至 2021 年 3 月期间接受 ACTH 治疗的 10 例婴儿痉挛诊断患者的病历。基础疾病包括颅内出血、缺氧缺血性脑病、结节性硬化症和脑梗死。给予的抗癫痫药物包括丙戊酸钠(VPA)、维生素 B6、唑尼沙胺、托吡酯、氯巴占、氯硝西泮和苯巴比妥。
10 例患者的中位年龄为 8 个月(4-17 个月),包括 8 例男性。ACTH 治疗前纤维蛋白原(Fbg)水平中位数为 202mg/dL(125-392mg/dL);然而,在中位 12 天(第 8-17 天)治疗期间,Fbg 水平显著下降至 108.5mg/dL(65-135mg/dL)(p<0.01)。无论是否联合 VPA,均观察到 Fbg 水平降低。这表明 ACTH 治疗可能影响 Fbg 水平,而与 VPA 联合使用无关。此外,与 ACTH 治疗前和 Fbg 水平最低时相比,凝血酶原时间和活化部分凝血活酶时间显著缩短。
无论是否联合 VPA,在 ACTH 治疗期间,尤其是在第二周,都需要密切监测凝血情况,以确保 ACTH 治疗的安全完成。