Miura Rina, Utano Tomoyuki, Miura Yoriko, Chiba Kyoko, Hasegawa Ayaka, Takafuji Yukiko, Takahashi Hayato, Tanzawa Ayano, Iwahashi Kana, Yamatani Akimasa, Yotani Nobuyuki
Department of Pharmaceuticals, National Center for Child Health and Development, Tokyo, Japan.
Division of Palliative Medicine, National Center of Child Health and Development, Tokyo, Japan.
J Palliat Med. 2024 Oct;27(10):1354-1358. doi: 10.1089/jpm.2024.0018. Epub 2024 Aug 9.
Naldemedine, a peripherally acting opioid μ receptor antagonist, is effective for prevention of opioid-induced constipation (OIC); however, evidence on its use in children is limited. To evaluate the efficacy and safety of naldemedine in pediatric patients with OIC. Retrospective analysis of 32 pediatric patients with OIC treated with naldemedine in a single institution in Japan from June 2017 to March 2021. Efficacy was evaluated in 13 evaluable patients with bowel movement (BM) response, defined as those with at least three BMs in the first 7 days after naldemedine initiation and an increase of at least one BM from baseline. Safety was evaluated by examining adverse events (AEs) based on the Common Terminology Criteria for AEs (v5.0). BM response was recorded in 11 of the 13 patients (85%), and the number BMs per day significantly increased from 0.43 before naldemedine to 1.00 after naldemedine ( = 0.025). The most common AE was diarrhea, observed in 16 of the 32 patients (50%), and all instances were grade 1 or 2. In three of the 16 patients, naldemedine was discontinued owing to worsening diarrhea. In pediatric patients, naldemedine resulted in a high rate of BM response and increased the BM frequency, indicating its efficacy. In some patients, grade 2 diarrhea required naldemedine discontinuation, suggesting that it should be used with caution in pediatric patients. Further studies are warranted to determine the optimal naldemedine dose in pediatric patients.
纳洛酮是一种外周作用的阿片类μ受体拮抗剂,对预防阿片类药物引起的便秘(OIC)有效;然而,其在儿童中的使用证据有限。为了评估纳洛酮在患有OIC的儿科患者中的疗效和安全性。对2017年6月至2021年3月在日本一家机构接受纳洛酮治疗的32例患有OIC的儿科患者进行回顾性分析。对13例可评估的有排便(BM)反应的患者进行疗效评估,BM反应定义为在开始使用纳洛酮后的前7天内至少有3次BM且比基线至少增加1次BM。通过根据不良事件通用术语标准(第5.0版)检查不良事件(AE)来评估安全性。13例患者中有11例(85%)记录到BM反应,每天的BM次数从使用纳洛酮前的0.43显著增加到使用纳洛酮后的1.00(P = 0.025)。最常见的AE是腹泻,32例患者中有16例(50%)出现,所有病例均为1级或2级。16例患者中有3例因腹泻加重而停用纳洛酮。在儿科患者中,纳洛酮导致较高的BM反应率并增加了BM频率,表明其疗效。在一些患者中,2级腹泻需要停用纳洛酮,这表明在儿科患者中应谨慎使用。有必要进行进一步研究以确定儿科患者中纳洛酮的最佳剂量。