Department of Nephrology & Hypertension, University Medical Centre Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, the Netherlands.
Julius Centre for Health Sciences and Primary Care, University Medical Centre Utrecht, Utrecht University, Utrecht, the Netherlands.
Syst Rev. 2022 Nov 12;11(1):238. doi: 10.1186/s13643-022-02108-x.
Patients with chronic kidney disease (CKD) require a personalised strategy for cardiovascular risk management (CVRM) to reduce their high risk of cardiovascular morbidity and mortality. Despite their high risk, patients with CKD appear to be underrepresented in randomised controlled trials (RCTs) for pharmacological CVRM interventions to reduce cardiovascular risk (pharmacological CVRM interventions). As a result, it remains unclear whether the efficacy of these interventions found in patients without CKD is similarly applicable to patients with CKD. This evidence map aims to provide an overview of the availability of the evidence from pharmacological CVRM trials for patients with CKD by assessing how often patients with reduced kidney function are specifically excluded or included from RCTs on pharmacological CVRM interventions and whether studies report efficacy estimates of interventions specifically for kidney patients.
We will perform a systematic literature search in ClinicalTrials.gov to identify relevant planned, ongoing, and completed RCTs on a broad range of CVRM medications after which we will retrieve the published protocols and papers via ClinicalTrials.gov itself, Embase, MEDLINE, or Google Scholar. We will include RCTs that investigate the efficacy of platelet inhibitors, anticoagulants, antihypertensives, glucose-lowering medication, and lipid-lowering medication on all-cause mortality, cardiovascular mortality, cardiovascular morbidity, and end-stage kidney disease in patients with a cardiovascular history or a major risk factor for cardiovascular disease. Two reviewers will independently screen trial records and their corresponding full-text publications to determine eligibility and extract data. Outcomes of interest are the exclusion of patients with reduced kidney function from RCTs and whether the study population was restricted to kidney patients or subgroup analyses were performed on kidney function. Results will be visualised in an evidence map.
The availability of evidence on the efficacy and safety of pharmacological CVRM interventions in patients with CKD might be limited. Hence, we will identify knowledge gaps for future research. At the same time, the availability of evidence, or lack thereof, might warrant caution from healthcare decision-makers in making strong recommendations based on the extrapolation of results from studies to patients who were explicitly excluded from participation.
PROSPERO CRD42022296746.
患有慢性肾病(CKD)的患者需要个性化的心血管风险管理(CVRM)策略,以降低其心血管发病率和死亡率的高风险。尽管他们的风险很高,但在用于降低心血管风险的药物 CVRM 干预的随机对照试验(RCT)中,CKD 患者的代表性似乎不足(药物 CVRM 干预)。因此,尚不清楚在没有 CKD 的患者中发现的这些干预措施的疗效是否同样适用于 CKD 患者。该证据图旨在通过评估肾功能下降的患者在药物 CVRM 干预 RCT 中被具体排除或纳入的频率,以及研究报告针对肾脏患者的干预措施的疗效估计值,来概述 CKD 患者的药物 CVRM 试验的证据可用性。
我们将在 ClinicalTrials.gov 中进行系统文献检索,以确定广泛的 CVRM 药物的相关计划、正在进行和已完成的 RCT,然后通过 ClinicalTrials.gov 本身、Embase、MEDLINE 或 Google Scholar 检索已发布的方案和论文。我们将纳入调查血小板抑制剂、抗凝剂、降压药、降血糖药和降血脂药对有心血管病史或心血管疾病主要危险因素的患者的全因死亡率、心血管死亡率、心血管发病率和终末期肾病疗效的 RCT。两名审查员将独立筛选试验记录及其相应的全文出版物,以确定资格并提取数据。感兴趣的结果是将肾功能下降的患者从 RCT 中排除,以及研究人群是否仅限于肾脏患者,或是否对肾功能进行了亚组分析。结果将以证据图的形式呈现。
CKD 患者药物 CVRM 干预的疗效和安全性证据可能有限。因此,我们将确定未来研究的知识空白。同时,证据的可用性或缺乏可能需要医疗保健决策者在根据研究结果向明确排除参与的患者进行外推时保持谨慎。
PROSPERO CRD42022296746。