Suppr超能文献

铁羧基麦芽糖在儿科胃肠病学中的应用:疗效确切,安全性无忧。

Ferric Carboxymaltose Across All Ages in Paediatric Gastroenterology Shows Efficacy Without Increased Safety Concerns.

机构信息

Royal Hospital for Children.

Public Health Scotland, Glasgow, UK.

出版信息

J Pediatr Gastroenterol Nutr. 2021 Apr 1;72(4):506-510. doi: 10.1097/MPG.0000000000003003.

Abstract

OBJECTIVES

The aim of the study was to assess the efficacy, safety and side-effect profile of ferric carboxymaltose (FCM) for correcting IDA in children and adolescents in paediatric gastroenterology, hepatology, and nutrition.

METHOD

This was a retrospective study of all gastroenterology patients <18 years who had FCM (October 2015 to October 2017). Haematological and biochemical parameters were recorded pre-infusion, at 4 weeks, 3 months, 6 months, and 1 year post-infusion. Recognised side-effects were documented.

RESULTS

Sixty-six children received FCM during this period. Data was analysed on 61 children, 5 excluded because of inadequate data. The median age at administration was 14 years (IQR 7). Thirty-two (52%) were boys. Twenty-six (42%) were <14 years old. Seven (11.5%) were <5 years old. Seventeen (28%) were switched from oral iron supplements to FCM. The median dose of FCM delivered was 19 mg/kg. The median haemoglobin increased from 108 to 126 g/L at 1 month post-infusion (P value <0.00001). The mean cell volume also improved from 80 to 84 fL at 1 month post-infusion (P value = 0.0007). Forty-eight (94%) children corrected their anaemia after receiving FCM. Two patients (3%) reported side-effects with skin bruising and staining.

CONCLUSIONS

FCM appears to be effective in correcting IDA in children across a wide range of gastroenterology indications and all ages. It is effective and generally well tolerated including in very young patients. Potential side-effects can be avoided by careful monitoring during infusions.

摘要

目的

本研究旨在评估羧基麦芽糖铁(FCM)治疗儿科胃肠病学、肝病学和营养学中儿童缺铁性贫血(IDA)的疗效、安全性和副作用特征。

方法

这是一项回顾性研究,纳入了所有在 2015 年 10 月至 2017 年 10 月期间接受 FCM 治疗的<18 岁胃肠病学患者。记录输注前、输注后 4 周、3 个月、6 个月和 1 年的血液学和生化参数。记录已知的副作用。

结果

在此期间,66 名儿童接受了 FCM 治疗。对 61 名儿童的数据进行了分析,5 名因数据不足而被排除。给药时的中位年龄为 14 岁(IQR 7)。32 名(52%)为男性。26 名(42%)<14 岁。7 名(11.5%)<5 岁。17 名(28%)从口服铁补充剂转为 FCM。给予的 FCM 中位剂量为 19mg/kg。血红蛋白中位数从输注后 1 个月的 108g/L 增加到 126g/L(P 值<0.00001)。平均细胞体积也从输注后 1 个月的 80fL 增加到 84fL(P 值=0.0007)。48 名(94%)儿童在接受 FCM 治疗后纠正了贫血。2 名患者(3%)报告有皮肤瘀伤和染色的副作用。

结论

FCM 似乎在纠正各种胃肠病学适应证和所有年龄段的儿童 IDA 方面均有效。它在包括非常年幼的患者在内的人群中有效且通常具有良好的耐受性。通过输注过程中的仔细监测,可以避免潜在的副作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验