Chin Med J (Engl). 1995 Sep;108(9):710-7.
Post-stroke Antihypertensive Treatment Study (PATS) was a randomized, double-blind and placebo-controlled trial, which aimed at determining whether antihypertensive treatment could reduce the risk of fatal and nonfatal stroke incidence in patients with a history of stroke or transient ischemic attack (TIA). 5,665 patients were randomized by a sealed envelope system. Systolic blood pressure (SBP) ranged from 80 to 280 mm Hg and diastolic (DBP) from 50 to 150 mmHg. The average SBP was 154 mmHg and average DBP 93 mmHg. The mean age was 60 years. Among the patients, women accounted for 28%. In 71% the latest stroke was ischemic. Average follow-up approximated to 2 years. The three-year average SBP was 149 mmHg for the placebo group and 144 mmHg for the indapamide treatment group, and the three-year DBP was 89 mmHg and 87 mmHg respectively. The three-year first incidence of fatal and nonfatal stroke was 12.3 per 100 patients placebo treatment and 9.4 per 100 with indapamide. The relative risk by proportional hazards regression analysis was 0.71 (P = 0.0009). For deaths from all causes, the relative risk was 0.91. (P > 0.05). The findings of this trial indicate that in patients with a history of stroke or TIA, blood pressure reduction of 5/2 mmHg with 2.5 mg indapamide reduced the first incidence of fatal and nonfatal stroke by 29%, with three-year absolute benefit of 29 events per 1000 participants.
卒中后降压治疗研究(PATS)是一项随机、双盲、安慰剂对照试验,旨在确定降压治疗是否能降低有卒中或短暂性脑缺血发作(TIA)病史患者发生致命性和非致命性卒中的风险。5665例患者通过密封信封系统进行随机分组。收缩压(SBP)范围为80至280mmHg,舒张压(DBP)范围为50至150mmHg。平均SBP为154mmHg,平均DBP为93mmHg。平均年龄为60岁。患者中女性占28%。71%的患者最新发作的卒中为缺血性。平均随访时间约为2年。安慰剂组三年平均SBP为149mmHg,吲达帕胺治疗组为144mmHg,三年DBP分别为89mmHg和87mmHg。安慰剂治疗组每100例患者中致命性和非致命性卒中的三年首次发生率为12.3例,吲达帕胺治疗组为9.4例。通过比例风险回归分析得出的相对风险为0.71(P = 0.0009)。对于所有原因导致的死亡,相对风险为0.91(P>0.05)。该试验结果表明,在有卒中或TIA病史的患者中,使用2.5mg吲达帕胺使血压降低5/2mmHg可使致命性和非致命性卒中的首次发生率降低29%,每1000名参与者的三年绝对获益为29例事件。