• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

日本胆道闭锁临床实践指南:英文简化版翻译的二次出版物。

Clinical practice guidelines for biliary atresia in Japan: A secondary publication of the abbreviated version translated into English.

机构信息

Aichi Developmental Disability Center, Kasugai, Japan.

Kumamoto Rosai Hospital, Yatsushiro, Japan.

出版信息

J Hepatobiliary Pancreat Sci. 2021 Jan;28(1):55-61. doi: 10.1002/jhbp.816. Epub 2020 Oct 4.

DOI:10.1002/jhbp.816
PMID:32780928
Abstract

The purpose of this study was to prepare clinical practice guidelines for biliary atresia according to the Medical Information Network Distribution Service (MINDS) Handbook for Clinical Practice Guideline Development 2014. The guideline drafting group determined 25 clinical questions (CQs) essential for daily clinical practice. These CQs were grouped into the following four major categories: diagnosis, treatment, complications, and prognosis. A systematic literature search was performed by the systematic review team, and medical evidence was extracted from articles published until July 2014 on PubMed and the Japan Medical Abstracts Society. To reach a consensus, majority voting (>70%) of the panel of the guideline drafting group was adopted according to the Delphi technique. Recommendations for 21 CQs were appropriately provided. However, for four CQs (CQ2, stool color; CQ9, steroid administration; and CQ24 and CQ25, liver transplantation), recommendations could not be determined due to a scarcity of evidence. The first clinical practice guidelines for biliary atresia were successfully created using procedures recommended by the MINDS. It is expected that these guidelines will be used worldwide, and that the standardization of biliary atresia treatment will improve treatment outcomes.

摘要

本研究旨在根据 2014 年《医疗信息网络分发服务(MINDS)临床实践指南制定手册》制定先天性胆道闭锁的临床实践指南。指南起草小组确定了 25 个对日常临床实践至关重要的临床问题(CQs)。这些 CQs 分为以下四个主要类别:诊断、治疗、并发症和预后。系统评价小组通过系统检索,从 2014 年 7 月前在 PubMed 和日本医学文摘学会上发表的文章中提取医学证据。为了达成共识,指南起草小组的专家小组采用了德尔菲技术的多数票(>70%)。对 21 个 CQs 提供了适当的建议。然而,由于证据不足,对于四个 CQs(CQ2、粪便颜色;CQ9、皮质类固醇治疗;CQ24 和 CQ25、肝移植),无法确定建议。本研究首次成功使用 MINDS 推荐的程序制定了先天性胆道闭锁的临床实践指南。预计这些指南将在全球范围内使用,胆道闭锁治疗的标准化将改善治疗结果。

相似文献

1
Clinical practice guidelines for biliary atresia in Japan: A secondary publication of the abbreviated version translated into English.日本胆道闭锁临床实践指南:英文简化版翻译的二次出版物。
J Hepatobiliary Pancreat Sci. 2021 Jan;28(1):55-61. doi: 10.1002/jhbp.816. Epub 2020 Oct 4.
2
Stool color card screening for early detection of biliary atresia and long-term native liver survival: a 19-year cohort study in Japan.粪便颜色卡筛查用于早期发现胆道闭锁和长期固有肝存活率:日本的一项 19 年队列研究。
J Pediatr. 2015 Apr;166(4):897-902.e1. doi: 10.1016/j.jpeds.2014.12.063. Epub 2015 Feb 11.
3
Japanese clinical practice guidelines for congenital biliary dilatation.日本先天性胆管扩张症临床实践指南。
J Hepatobiliary Pancreat Sci. 2017 Jan;24(1):1-16. doi: 10.1002/jhbp.415. Epub 2017 Jan 22.
4
Evidence-based diagnosis and clinical practice guidelines for intestinal Behçet's disease 2020 edited by Intractable Diseases, the Health and Labour Sciences Research Grants.《2020 年肠型贝赫切特病循证诊断与临床实践指南》,特发性疾病,健康与劳动科学研究补助金编辑。
J Gastroenterol. 2020 Jul;55(7):679-700. doi: 10.1007/s00535-020-01690-y. Epub 2020 May 7.
5
Biliary atresia in Vietnam: Management and the burden of disease.越南的胆道闭锁:疾病管理与负担
Surgery. 2017 Feb;161(2):533-537. doi: 10.1016/j.surg.2016.08.012. Epub 2016 Oct 13.
6
Evidence-based clinical practice guideline for adult Still's disease.成人斯蒂尔病的循证临床实践指南
Mod Rheumatol. 2018 Sep;28(5):736-757. doi: 10.1080/14397595.2018.1465633. Epub 2018 May 9.
7
A multicenter study of primary liver transplantation for biliary atresia in Japan.日本一项关于胆道闭锁的原位肝移植的多中心研究。
Pediatr Surg Int. 2019 Nov;35(11):1223-1229. doi: 10.1007/s00383-019-04553-7. Epub 2019 Sep 18.
8
Japanese Orthopaedic Association (JOA) clinical practice guidelines on the management of soft tissue tumors 2020 - Secondary publication.日本矫形外科学会(JOA)软组织肿瘤治疗指南 2020 年版 - 二次出版
J Orthop Sci. 2022 May;27(3):533-550. doi: 10.1016/j.jos.2021.11.023. Epub 2022 Mar 23.
9
The Japanese breast cancer society clinical practice guidelines for radiation treatment of breast cancer, 2022 edition.日本乳腺癌学会《乳腺癌放射治疗临床实践指南(2022年版)》
Breast Cancer. 2024 May;31(3):347-357. doi: 10.1007/s12282-024-01568-4. Epub 2024 Apr 5.
10
Effects of age at Kasai portoenterostomy on the surgical outcome: a review of the literature.肝门空肠吻合术年龄对手术结果的影响:文献综述
Surg Today. 2015 Jul;45(7):813-8. doi: 10.1007/s00595-014-1024-z. Epub 2014 Sep 12.

引用本文的文献

1
Dosage and duration of ursodeoxycholic acid therapy Post-Kasai portoenterostomy in biliary atresia: a multicenter cross-sectional study with age stratification.熊去氧胆酸治疗的剂量和持续时间:胆管闭锁患儿肝门空肠吻合术后的多中心分层横断面研究
Pediatr Surg Int. 2025 Aug 30;41(1):279. doi: 10.1007/s00383-025-06180-x.
2
Japanese biliary atresia registry.日本胆道闭锁登记处。
World J Pediatr Surg. 2025 May 26;8(2):e001024. doi: 10.1136/wjps-2025-001024. eCollection 2025.
3
Generation of human induced pluripotent stem cell lines derived from patients of cystic biliary atresia.
从囊性胆管闭锁患者中生成的人类诱导多能干细胞系。
Hum Cell. 2024 Nov 13;38(1):18. doi: 10.1007/s13577-024-01147-x.
4
Biliary fibrosis is an important but neglected pathological feature in hepatobiliary disorders: from molecular mechanisms to clinical implications.胆汁纤维化是肝胆疾病中一个重要但被忽视的病理特征:从分子机制到临床意义。
Med Rev (2021). 2024 Jul 1;4(4):326-365. doi: 10.1515/mr-2024-0029. eCollection 2024 Aug.
5
Serum matrix metalloproteinase-7 for discriminating biliary atresia: a diagnostic accuracy and validation study.血清基质金属蛋白酶-7鉴别先天性胆道闭锁:一项诊断准确性和验证研究。
J Transl Med. 2024 Jul 8;22(1):636. doi: 10.1186/s12967-024-05442-x.
6
Progress in Biomarkers Related to Biliary Atresia.与胆道闭锁相关的生物标志物研究进展
J Clin Transl Hepatol. 2024 Mar 28;12(3):305-315. doi: 10.14218/JCTH.2023.00260. Epub 2024 Jan 30.
7
Measurement of MMP-7 in micro-volume peripheral blood: development of dried blood spot approach.微量外周血中基质金属蛋白酶-7的检测:干血斑法的开发
Front Pediatr. 2023 Nov 15;11:1293329. doi: 10.3389/fped.2023.1293329. eCollection 2023.
8
Prednisolone administration monitored by postoperative stool color achieves high jaundice clearance after laparoscopic portoenterostomy for biliary atresia.通过术后大便颜色监测泼尼松龙给药,在腹腔镜下进行胆管闭锁的肝门空肠吻合术后可实现高黄疸清除率。
Pediatr Surg Int. 2023 Nov 20;39(1):299. doi: 10.1007/s00383-023-05580-1.
9
Immune-mediated cholangiopathies in children: the need to better understand the pathophysiology for finding the future possible treatment targets.儿童免疫介导性胆管病:为寻找未来可能的治疗靶点,需要更好地了解其病理生理学。
Front Immunol. 2023 Oct 20;14:1206025. doi: 10.3389/fimmu.2023.1206025. eCollection 2023.
10
Percutaneous Transhepatic Biliary Intervention in Adult Biliary Atresia Patients After Kasai Portoenterostomy.肝门空肠吻合术后成人胆道闭锁患者的经皮经肝胆道介入治疗
JPGN Rep. 2022 May 9;3(2):e206. doi: 10.1097/PG9.0000000000000206. eCollection 2022 May.