The Ottawa Hospital and the University of Ottawa, 1967 Riverside Drive, Ottawa, ON, K1H7W9, Canada.
Department of Global Health and Social Medicine, Harvard Medical School, Boston, MA, 02115, USA.
Syst Rev. 2018 Feb 21;7(1):34. doi: 10.1186/s13643-018-0701-1.
Contrast-induced acute kidney injury (CI-AKI) is defined as worsening of renal function after the administration of iodinated contrast material. In patients with cardiovascular disease, kidney disease, and/or diabetes, renin-angiotensin system blockers, non-steroidal anti-inflammatory drugs, diuretics, and metformin can increase the risk of CI-AKI when undergoing contrast imaging. Despite CI-AKI being the leading iatrogenic cause of acute kidney injury, there is a lack of sufficient scientific evidence supporting which drugs should be stopped, when they should be stopped, and when they should be resumed. The purpose of this systematic review is to assess (1) the effect of withholding medication before contrast procedures on the risk of CI-AKI and other clinical outcomes and (2) the incidence of adverse events occurring after withholding these drugs prior to contrast procedures. This protocol has been registered with PROSPERO, https://www.crd.york.ac.uk/PROSPERO/display_record.asp?ID=CRD42016033178 .
An information specialist will assist in searching MEDLINE, Embase, and the Cochrane Library databases to identify randomized controlled trials, observational studies, case reports, and case series. Relevant abstracts from professional society meetings and web-based registries of clinical trials will also be included. Studies included will compare patients aged ≥ 18 years instructed to continue taking the drugs of interest and those advised to stop taking them before undergoing contrast procedures. If these drugs are not withheld prior to contrast procedures, the studies must compare patients who are administered these drugs and those who are not before undergoing contrast procedures. Two reviewers will independently screen the titles and abstracts of the studies obtained from the search using pre-defined inclusion criteria and will then extract data from the full texts of selected studies. The quality of the studies will be assessed by two independent reviewers using the Cochrane Risk of Bias 2.0 tool for randomized trials and the Newcastle-Ottawa Scale for observational studies.
This systematic review will provide a synthesis of current evidence on the discontinuation of drugs prior to contrast procedures and its effect on CI-AKI and other clinical outcomes. These findings will provide clinicians with guidelines and serve as a strong research base for future studies in this field.
PROSPERO CRD42016033178.
对比剂诱导的急性肾损伤(CI-AKI)是指在使用碘造影剂后肾功能恶化。在患有心血管疾病、肾脏疾病和/或糖尿病的患者中,肾素-血管紧张素系统阻滞剂、非甾体抗炎药、利尿剂和二甲双胍在接受造影成像时会增加 CI-AKI 的风险。尽管 CI-AKI 是医源性急性肾损伤的主要原因,但缺乏足够的科学证据支持应该停止哪些药物、何时停止以及何时恢复使用。本系统评价的目的是评估(1)在对比检查前停止用药对 CI-AKI 和其他临床结局的影响,以及(2)在对比检查前停止这些药物后发生不良事件的发生率。本方案已在 PROSPERO 注册,网址为:https://www.crd.york.ac.uk/PROSPERO/display_record.asp?ID=CRD42016033178。
信息专家将协助检索 MEDLINE、Embase 和 Cochrane 图书馆数据库,以确定随机对照试验、观察性研究、病例报告和病例系列。还将纳入专业学会会议的相关摘要和临床试验的网络注册。纳入的研究将比较告知继续服用感兴趣药物的年龄≥18 岁的患者和被建议在接受对比检查前停止服用这些药物的患者。如果这些药物在接受对比检查前没有被停用,则这些研究必须比较接受这些药物和未接受这些药物的患者。两名评审员将独立使用预定义的纳入标准筛选检索到的研究的标题和摘要,然后从选定研究的全文中提取数据。使用 Cochrane 偏倚风险 2.0 工具对随机试验和纽卡斯尔-渥太华量表对观察性研究对研究进行质量评估。
本系统评价将综合目前关于对比检查前停药及其对 CI-AKI 和其他临床结局影响的证据。这些发现将为临床医生提供指南,并为该领域未来的研究提供有力的研究基础。
PROSPERO CRD42016033178。