Zhu Jiaying, Chen Ning, Zhou Muke, Guo Jian, Zhu Cairong, Zhou Jie, Ma Mengmeng, He Li
Department of Neurology, West China Hospital, Sichuan University, Chengdu, China.
Department of Emergency, Gui Zhou Provincial People's Hospital, Guiyang, China.
Cochrane Database Syst Rev. 2022 Jan 9;1(1):CD003654. doi: 10.1002/14651858.CD003654.pub6.
This is the first update of a review published in 2010. While calcium channel blockers (CCBs) are often recommended as a first-line drug to treat hypertension, the effect of CCBs on the prevention of cardiovascular events, as compared with other antihypertensive drug classes, is still debated.
To determine whether CCBs used as first-line therapy for hypertension are different from other classes of antihypertensive drugs in reducing the incidence of major adverse cardiovascular events.
For this updated review, the Cochrane Hypertension Information Specialist searched the following databases for randomised controlled trials (RCTs) up to 1 September 2020: the Cochrane Hypertension Specialised Register, the Cochrane Central Register of Controlled Trials (CENTRAL 2020, Issue 1), Ovid MEDLINE, Ovid Embase, the World Health Organization International Clinical Trials Registry Platform, and ClinicalTrials.gov. We also contacted the authors of relevant papers regarding further published and unpublished work and checked the references of published studies to identify additional trials. The searches had no language restrictions.
Randomised controlled trials comparing first-line CCBs with other antihypertensive classes, with at least 100 randomised hypertensive participants and a follow-up of at least two years.
Three review authors independently selected the included trials, evaluated the risk of bias, and entered the data for analysis. Any disagreements were resolved through discussion. We contacted study authors for additional information.
This update contains five new trials. We included a total of 23 RCTs (18 dihydropyridines, 4 non-dihydropyridines, 1 not specified) with 153,849 participants with hypertension. All-cause mortality was not different between first-line CCBs and any other antihypertensive classes. As compared to diuretics, CCBs probably increased major cardiovascular events (risk ratio (RR) 1.05, 95% confidence interval (CI) 1.00 to 1.09, P = 0.03) and increased congestive heart failure events (RR 1.37, 95% CI 1.25 to 1.51, moderate-certainty evidence). As compared to beta-blockers, CCBs reduced the following outcomes: major cardiovascular events (RR 0.84, 95% CI 0.77 to 0.92), stroke (RR 0.77, 95% CI 0.67 to 0.88, moderate-certainty evidence), and cardiovascular mortality (RR 0.90, 95% CI 0.81 to 0.99, low-certainty evidence). As compared to angiotensin-converting enzyme (ACE) inhibitors, CCBs reduced stroke (RR 0.90, 95% CI 0.81 to 0.99, low-certainty evidence) and increased congestive heart failure (RR 1.16, 95% CI 1.06 to 1.28, low-certainty evidence). As compared to angiotensin receptor blockers (ARBs), CCBs reduced myocardial infarction (RR 0.82, 95% CI 0.72 to 0.94, moderate-certainty evidence) and increased congestive heart failure (RR 1.20, 95% CI 1.06 to 1.36, low-certainty evidence).
AUTHORS' CONCLUSIONS: For the treatment of hypertension, there is moderate certainty evidence that diuretics reduce major cardiovascular events and congestive heart failure more than CCBs. There is low to moderate certainty evidence that CCBs probably reduce major cardiovascular events more than beta-blockers. There is low to moderate certainty evidence that CCBs reduced stroke when compared to angiotensin-converting enzyme (ACE) inhibitors and reduced myocardial infarction when compared to angiotensin receptor blockers (ARBs), but increased congestive heart failure when compared to ACE inhibitors and ARBs. Many of the differences found in the current review are not robust, and further trials might change the conclusions. More well-designed RCTs studying the mortality and morbidity of individuals taking CCBs as compared with other antihypertensive drug classes are needed for patients with different stages of hypertension, different ages, and with different comorbidities such as diabetes.
这是对2010年发表的一篇综述的首次更新。虽然钙通道阻滞剂(CCB)常被推荐作为治疗高血压的一线药物,但与其他类别的抗高血压药物相比,CCB对预防心血管事件的效果仍存在争议。
确定作为高血压一线治疗药物的CCB在降低主要不良心血管事件发生率方面是否与其他类别的抗高血压药物不同。
对于本次更新的综述,Cochrane高血压信息专家检索了以下数据库以查找截至2020年9月1日的随机对照试验(RCT):Cochrane高血压专业注册库、Cochrane对照试验中心注册库(CENTRAL 2020年第1期)、Ovid MEDLINE、Ovid Embase、世界卫生组织国际临床试验注册平台和ClinicalTrials.gov。我们还联系了相关论文的作者以获取更多已发表和未发表的研究,并查阅已发表研究的参考文献以识别其他试验。检索无语言限制。
将一线CCB与其他抗高血压药物类别进行比较的随机对照试验,至少有100名随机分组的高血压参与者,且随访至少两年。
三位综述作者独立选择纳入的试验,评估偏倚风险,并录入数据进行分析。任何分歧均通过讨论解决。我们联系研究作者以获取更多信息。
本次更新纳入了五项新试验。我们共纳入了23项RCT(18项二氢吡啶类、4项非二氢吡啶类、1项未明确类别),涉及153849名高血压参与者。一线CCB与其他任何抗高血压药物类别在全因死亡率方面无差异。与利尿剂相比,CCB可能增加主要心血管事件(风险比(RR)1.05,95%置信区间(CI)1.00至1.09,P = 0.03)和增加充血性心力衰竭事件(RR 1.37,95%CI 1.25至1.51,中等确定性证据)。与β受体阻滞剂相比,CCB降低了以下结局:主要心血管事件(RR 0.84,95%CI 0.77至0.92)、中风(RR 0.77,95%CI 0.67至0.88,中等确定性证据)和心血管死亡率(RR 0.90,95%CI 0.81至0.99,低确定性证据)。与血管紧张素转换酶(ACE)抑制剂相比,CCB降低了中风(RR 0.90,95%CI 0.81至0.99,低确定性证据)并增加了充血性心力衰竭(RR 1.16,95%CI 1.06至1.28,低确定性证据)。与血管紧张素受体阻滞剂(ARB)相比,CCB降低了心肌梗死(RR 0.82,95%CI 0.72至0.94,中等确定性证据)并增加了充血性心力衰竭(RR 1.20,95%CI 1.06至1.36,低确定性证据)。
对于高血压治疗,有中等确定性证据表明利尿剂比CCB更能降低主要心血管事件和充血性心力衰竭。有低到中等确定性证据表明CCB可能比β受体阻滞剂更能降低主要心血管事件。有低到中等确定性证据表明与血管紧张素转换酶(ACE)抑制剂相比CCB降低了中风,与血管紧张素受体阻滞剂(ARB)相比降低了心肌梗死,但与ACE抑制剂和ARB相比增加了充血性心力衰竭。当前综述中发现的许多差异并不稳健,进一步的试验可能会改变结论。对于不同高血压阶段、不同年龄以及患有不同合并症(如糖尿病)的患者,需要更多设计良好的RCT来研究服用CCB与其他抗高血压药物类别的个体的死亡率和发病率。