Atkins Emily R, Rodgers Anthony
The George Institute for Global Health, The University of Sydney, Sydney, Australia.
The George Institute for Global Health, The University of Sydney, Sydney, Australia.
Clin Ther. 2016 Oct;38(10):2135-2141. doi: 10.1016/j.clinthera.2016.08.007. Epub 2016 Sep 12.
This article summarizes the results of a recent systematic review and meta-analysis of the safety and efficacy of intensive blood pressure (BP) lowering, including an update with the SPRINT (Systolic Blood Pressure Intervention Trial) results. We discuss the consistency of results within this set of trials (eg, ACCORD [Action to Control Cardiovascular Risk in Diabetes] and SPRINT) and the results in the context of other BP-lowering trials, including the recently published HOPE3 (Heart Outcomes Prevention Evaluation-3) study.
This study was a narrative review with updated meta-analysis from systematic review of trials comparing more- versus less-intensive BP lowering.
With the addition of SPRINT, there are >20 trials comparing more- versus less-intensive treatment with 54,350 participants overall. Over an average of 3.9 years of follow-up, the average systolic BP was 133 mm Hg in the more-intensive treatment arms and 140 mm Hg in the less-intensive treatment arms. More-intensive BP lowering reduced the risk of major vascular events, with benefits seen across a range of groups defined according to baseline systolic BP (120-139 mm Hg, 140-159 mm Hg, or ≥160 mm Hg), age (<70 or >70 years), and main entry criterion (hypertension, diabetes, or renal disease).
The evidence accumulated thus far provides clear evidence of the benefits of BP lowering in the 120- to 140-mm Hg range for various high-risk patient groups. Although intensive BP lowering has side effects, these trials indicate that the benefits will predominate for those at high risk of major vascular events.
本文总结了近期一项关于强化降压安全性和有效性的系统评价及荟萃分析的结果,包括纳入收缩压干预试验(SPRINT)结果后的更新内容。我们讨论了这组试验(如糖尿病心血管风险控制行动[ACCORD]和SPRINT)结果的一致性,以及在其他降压试验背景下的结果,包括最近发表的心脏结局预防评估-3(HOPE3)研究。
本研究是一项叙述性综述,并对比较强化与非强化降压的试验进行系统评价后更新了荟萃分析。
纳入SPRINT后,有超过20项试验比较了强化与非强化治疗,共有54350名参与者。平均随访3.9年,强化治疗组的平均收缩压为133mmHg,非强化治疗组为140mmHg。强化降压降低了主要血管事件的风险,在根据基线收缩压(120 - 139mmHg、140 - 159mmHg或≥160mmHg)、年龄(<70岁或>70岁)和主要入选标准(高血压、糖尿病或肾病)定义的一系列人群中均观察到益处。
迄今为止积累的证据清楚地表明,对于各种高危患者群体,将血压降至120至140mmHg范围有益处。尽管强化降压有副作用,但这些试验表明,对于那些有主要血管事件高风险的患者,益处将占主导。