Jinwen Ni, Bingyan Cao, He Zeng, Chunxiu Gong, Feihong Luo
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Common side effects were hepatobiliary injuries (20.5%), gastrointestinal symptoms (31.1%), and transient hyperglycaemia (49.2%), with one case of necrotizing enterocolitis. Adverse event rates increased in patients treated with intermediate octreotide dose to those treated with higher doses, rising from 58% at doses of 5-10 µg/kg/day to 100% at doses exceeding 20 µg/kg/day. Patients experiencing adverse events received significantly higher doses.</p><p><strong>Conclusion: </strong>Octreotide effectively maintained blood glucose levels in diazoxide-unresponsive CHI patients without serious adverse effects, across all subtypes. Our study suggests that intermediate octreotide dosing is associated with a lower incidence of adverse events. 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引用次数: 0
摘要
奥曲肽被推荐作为先天性胰岛素分泌过多症(CHI)患者的二线治疗方法,尤其是那些对地佐米或手术治疗无效的患者。有关奥曲肽不良反应的大样本研究仍然很少。我们通过回顾中国两家最大的专业治疗 CHI 中心的病例,评估了奥曲肽在 CHI 患者中的安全性。我们的研究分析了122例接受奥曲肽治疗的CHI患者的不良事件,其中单独治疗的成功率为93%。奥曲肽的平均最大剂量为 13.1 ± 6.5 µg/kg/天,弥漫性和局灶性病变患者所需的剂量没有差异。常见的副作用为肝胆损伤(20.5%)、胃肠道症状(31.1%)和一过性高血糖(49.2%),其中一例为坏死性小肠结肠炎。接受中等剂量奥曲肽治疗的患者发生不良反应的比例从58%(5-10微克/千克/天)上升到100%(20微克/千克/天)。出现不良反应的患者接受的剂量明显更高:结论:在所有亚型中,奥曲肽能有效维持对二氮卓无反应的CHI患者的血糖水平,且无严重不良反应。我们的研究表明,中等剂量的奥曲肽可降低不良反应的发生率。我们建议对接受奥曲肽治疗的患者进行密切监测,尤其是在起始阶段和使用较大剂量时:- 奥曲肽是先天性高胰岛素血症患者常用的二线治疗药物。- 新发现:我们的研究表明,奥曲肽是治疗先天性高胰岛素血症的常用二线药物:- 我们的研究表明,奥曲肽可用于维持健康状况良好的先天性高胰岛素血症婴儿的血糖水平,且无严重不良反应。- 接受奥曲肽治疗的患者的不良反应发生率与剂量有关。
Octreotide efficacy and safety in children with hyperinsulinism: evidence from two Chinese centers.
Octreotide is recommended as a second-line treatment for patients with congenital hyperinsulinism (CHI), especially for those who do not respond to diazoxide or surgical intervention. Studies on the adverse effects of octreotide in large cohorts are still scarce. We evaluated the safety of octreotide in CHI patients by reviewing cases from the two largest centres in China that specialize in the management of this condition. Our study analysed adverse events in 122 CHI patients on octreotide, with a 93% success rate for the therapy alone. The mean maximum dose of octreotide was 13.1 ± 6.5 µg/kg/day, with no difference in required doses between diffuse and focal lesion patients. Common side effects were hepatobiliary injuries (20.5%), gastrointestinal symptoms (31.1%), and transient hyperglycaemia (49.2%), with one case of necrotizing enterocolitis. Adverse event rates increased in patients treated with intermediate octreotide dose to those treated with higher doses, rising from 58% at doses of 5-10 µg/kg/day to 100% at doses exceeding 20 µg/kg/day. Patients experiencing adverse events received significantly higher doses.
Conclusion: Octreotide effectively maintained blood glucose levels in diazoxide-unresponsive CHI patients without serious adverse effects, across all subtypes. Our study suggests that intermediate octreotide dosing is associated with a lower incidence of adverse events. We recommend close monitoring of patients receiving octreotide, especially during the initiation phase and when higher doses are administered.
What is known: • Octreotide is a commonly used second line treatment for patients with congenital hyperinsulinism. • The administration of octreotide is frequently associated with gastrointestinal adverse events.
What is new: • Our study indicates that octreotide is used without serious adverse effects to maintain blood glucose levels in infants with congenital hyperinsulinism who are otherwise in good health. • The incidence of adverse events in patients treated with octreotide is dose-dependent.
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