Suppr超能文献

关于化疗引起的恶心和呕吐的止吐处方的全区域专业实践评估

[Region-wide professional practice evaluation with regards to antiemetic prescription into chemotherapy-induced nausea and vomiting].

作者信息

Tavernier Jérôme, Jouannet-Romaszko Mireille, Bertucat Helena, Marchiset Nathalie, Bahadoor Mohum, Chevrier Régine

机构信息

Centre hospitalier de Vichy, boulevard Denière, 03200 Vichy, France.

CHU de Clermont-Ferrand, rue Montalembert, 63000 Clermont-Ferrand, France.

出版信息

Bull Cancer. 2016 Jul-Aug;103(7-8):622-31. doi: 10.1016/j.bulcan.2016.03.009. Epub 2016 May 10.

Abstract

The anticancer drug technical commission (COTECH) of the Auvergne OMEDIT has set up a region-wide professional practice evaluation (PPE) with regards to antiemetic prescription practices in chemotherapy-induced nausea and vomiting (CINV), in order to evaluate their compliance with OMEDIT's guidelines. Are not included pediatric and hematologic protocols. A prospective survey was carried from November 2013 to January 2014 out in 14 medical centers in Auvergne. This clinical audit was based on the HAS (national healthcare authority) framework and used as a reference regional standards based on the MASCC Antiemetic Guidelines. Altogether, 346 antiemetic prescriptions were compared to guidelines. We observed respectively 81 % and 42 % conformity rates in acute and delayed emesis for high emesis risk chemotherapy (HE); 86 % and 35 % conformity rates in acute and delayed emesis for moderate emesis risk chemotherapy (ME); 66 % and 85 % conformity rates in acute and delayed emesis for low emesis risk chemotherapy (LE). These results highlight deficiencies in compliance with guidelines, especially in the management of delayed CINV in HE and ME chemotherapy. The COTECH identified three priority improvement areas: under-prescribe NK1 antagonists in HE cure; under-prescribe corticosteroid; over-prescribe 5HT3 antagonists for delayed emesis. The COTECH is publicizing these results all over the Auvergne region, together with a reminder of recommendations.

摘要

奥弗涅大区肿瘤医学组织(OMEDIT)的抗癌药物技术委员会(COTECH)针对化疗引起的恶心和呕吐(CINV)的止吐处方实践开展了一项全区域的专业实践评估(PPE),以评估其是否符合OMEDIT的指南。儿科和血液学方案不包括在内。2013年11月至2014年1月在奥弗涅大区的14家医疗中心进行了一项前瞻性调查。这项临床审计基于法国国家卫生管理局(HAS)的框架,并以基于MASCC止吐指南的区域标准作为参考。总共将346份止吐处方与指南进行了比较。我们观察到,对于高致吐风险化疗(HE),急性和延迟性呕吐的符合率分别为81%和42%;对于中度致吐风险化疗(ME),急性和延迟性呕吐的符合率分别为86%和35%;对于低致吐风险化疗(LE),急性和延迟性呕吐的符合率分别为66%和85%。这些结果凸显了在遵循指南方面存在的不足,尤其是在HE和ME化疗中延迟性CINV的管理方面。COTECH确定了三个优先改进领域:在HE治疗中NK1拮抗剂处方不足;皮质类固醇处方不足;对于延迟性呕吐5HT3拮抗剂处方过量。COTECH正在奥弗涅大区全境公布这些结果,并同时提醒大家注意相关建议。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验