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替度鲁肽在儿童肠衰竭中的应用:一项系统评价。

Use of Teduglutide in Children With Intestinal Failure: A Systematic Review.

作者信息

Gigola Francesca, Cianci Maria Chiara, Cirocchi Roberto, Ranucci Maria Chiara, Del Riccio Marco, Coletta Riccardo, Morabito Antonino

机构信息

Department of Pediatric Surgery, Meyer Children's Hospital Academic Centre, Florence, Italy.

Department of Medicine and Surgery, University of Perugia, Perugia, Italy.

出版信息

Front Nutr. 2022 Jun 14;9:866518. doi: 10.3389/fnut.2022.866518. eCollection 2022.

Abstract

BACKGROUND AND OBJECTIVES

Short-bowel syndrome (SBS) results from the loss of a significant portion of the small intestine leading to a state of malabsorption. After an intestinal loss, there is a process of adaptation involving the Glucagon-Like Peptide-2 (GLP-2), an enteroendocrine peptide also involved in nutrient absorption. Teduglutide is a recombinant analog of GLP-2 approved in 2016 to treat selected SBS pediatric patients who are dependent on parenteral support. The present systematic review aims to evaluate the efficacy of Teduglutide in pediatric patients with SBS in reducing the need for parenteral nutrition (PN).

MATERIALS AND METHODS

We performed a literature search on MEDLINE and Embase to include articles up to November 2021. We included articles that involved using Teduglutide in the SBS pediatric population to define its efficacy in reducing the need for PN. The key words used were GLP-2, teduglutide, child.

RESULTS

Fourteen studies completely fulfilled the inclusion criteria. Two hundred 23 patients were treated with Teduglutide, and the median duration of treatment was 45 weeks (IQR: 36-52.5 weeks). One-hundred and fifty-two patients were treated with 0.05 mg/Kg/d of subcutaneous Teduglutide, 38 received 0.025 mg/Kg/d and 8 received either 0.125 mg/Kg/d or 0.20 mg/Kg/d. A total of 36 patients achieved enteral autonomy (EA) after a median of 24 weeks of treatment (IQR: 24-48 weeks) and 149 patients showed a reduction in PN needs in terms of volume, calories, or hours per day. Eleven studies reported complications: gastrointestinal were the most common, with 89 cases reported in treated patients and 11 in non-treated patients.

CONCLUSION

Teduglutide appears safe and effective in reducing PN requirements and improving EA in the pediatric population. However, more studies are needed to understand its efficacy in the long term and after discontinuation and possible complications.

SYSTEMATIC REVIEW REGISTRATION

[https://www.crd.york.ac.uk/prospero/], identifier [CRD42022301593].

摘要

背景与目的

短肠综合征(SBS)是由于小肠大部分缺失导致吸收不良状态。肠道缺失后,会发生一个涉及胰高血糖素样肽-2(GLP-2)的适应过程,GLP-2是一种也参与营养吸收的肠内分泌肽。替度鲁肽是一种GLP-2重组类似物,于2016年获批用于治疗某些依赖肠外支持的SBS儿科患者。本系统评价旨在评估替度鲁肽在SBS儿科患者中减少肠外营养(PN)需求的疗效。

材料与方法

我们在MEDLINE和Embase上进行了文献检索,纳入截至2021年11月的文章。我们纳入了涉及在SBS儿科人群中使用替度鲁肽以确定其减少PN需求疗效的文章。使用的关键词为GLP-2、替度鲁肽、儿童。

结果

14项研究完全符合纳入标准。232例患者接受了替度鲁肽治疗,中位治疗持续时间为45周(四分位间距:36 - 52.5周)。152例患者接受皮下注射替度鲁肽0.05 mg/Kg/d治疗,38例接受0.025 mg/Kg/d治疗,8例接受0.125 mg/Kg/d或0.20 mg/Kg/d治疗。共有36例患者在中位治疗24周(四分位间距:24 - 48周)后实现肠内自主(EA),149例患者在PN的量、热量或每日使用时长方面需求减少。11项研究报告了并发症:胃肠道并发症最为常见,治疗患者中报告89例,未治疗患者中报告11例。

结论

替度鲁肽在减少儿科人群PN需求和改善EA方面似乎安全有效。然而,需要更多研究来了解其长期疗效、停药后疗效以及可能的并发症。

系统评价注册

[https://www.crd.york.ac.uk/prospero/],标识符[CRD42022301593]

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4ac/9237607/0c269b912df1/fnut-09-866518-g001.jpg

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