Hansson L, Zanchetti A
Department of Geriatrics, University of Uppsala, Sweden.
Blood Press. 1997 Sep;6(5):313-7. doi: 10.3109/08037059709062088.
The Hypertension Optimal Treatment (HOT) Study is an ongoing prospective randomized, multicentre trial conducted in 26 countries. There are two main aims of the study. The first is to evaluate the relationship between three levels of target diastolic blood pressure (< or = 90, < or = 85 or < or = 80 mmHg) and the incidence of cardiovascular morbidity and mortality in hypertensive patients. The second is to determine the effect on morbidity and mortality of a low dose, 75 mg daily, of acetylsalicylic acid (ASA, aspirin) compared with placebo. Altogether 18,790 patients have been recruited and randomized, and two-year data are now available for all patients. This is a report on the blood pressures achieved, the tolerability, and other available data after 24 months of follow-up of all patients. Special emphasis is given to the subgroup of elderly patients (> or = 65 years, n = 5988) compared with young patients (< 65 years, n = 12 802). On average, patients in the < or = 90 mmHg diastolic blood pressure target group have reached 85 mmHg, in the < or = 85 mmHg target group patients have reached 83 mmHg and in the < or = 80 mmHg target group patients have reached 81 mmHg. The percentage of those achieving target blood pressure in each target group at 24 months of follow-up is 85% in the < or = 90 mmHg target group, 75% in the < or = 85 mmHg target group and 57% in the < or = 80 mmHg target group. In the elderly subgroup (> or = 65 years of age), the percentage of patients achieving target at 24 months is higher for all target groups, namely 89% in the < or = 90 mmHg group, 80% in the 85 mmHg group and 62% in the 80 mmHg group. Antihypertensive treatment was initiated with a calcium antagonist, felodipine, at a dose of 5 mg once daily. If target blood pressure was not reached, additional antihypertensive therapy, with either an angiotensin converting enzyme (ACE) inhibitor or a beta-adrenoceptor blocking agent, was given. Further dose adjustments were made in accordance with a set protocol. As a fifth, and final, step, a diuretic could be added. There have been relatively few side effects in this large, multinational study of hypertensive patients. Only ankle oedema and coughing exceed a frequency of 0.5% (ankle oedema 1.3% in young and 1.7% in elderly; coughing 0.5% in young and elderly). After two years, 84% of all patients are still taking their baseline therapy, felodipine. The 24-month data presented here indicate that it should be possible to fulfil the primary aims of the HOT Study.
高血压最佳治疗(HOT)研究是一项正在进行的前瞻性随机多中心试验,在26个国家开展。该研究有两个主要目标。第一个目标是评估三个舒张压目标水平(≤90、≤85或≤80 mmHg)与高血压患者心血管发病和死亡发生率之间的关系。第二个目标是确定与安慰剂相比,每日75 mg低剂量乙酰水杨酸(ASA,阿司匹林)对发病和死亡的影响。总共招募并随机分配了18790名患者,目前所有患者的两年数据均已可得。这是一份关于所有患者随访24个月后所达到的血压、耐受性及其他可用数据的报告。特别强调了老年患者亚组(≥65岁,n = 5988)与年轻患者(<65岁,n = 12802)的比较。平均而言,舒张压目标为≤90 mmHg组的患者达到了85 mmHg,≤85 mmHg目标组的患者达到了83 mmHg,≤80 mmHg目标组的患者达到了81 mmHg。在随访24个月时,各目标组中达到目标血压的患者百分比在≤90 mmHg目标组为85%,≤85 mmHg目标组为75%,≤80 mmHg目标组为57%。在老年亚组(≥65岁)中,所有目标组在24个月时达到目标的患者百分比更高,即≤90 mmHg组为89%,85 mmHg组为80%,80 mmHg组为62%。抗高血压治疗起始采用钙拮抗剂非洛地平,剂量为每日5 mg一次。如果未达到目标血压,则加用其他抗高血压药物,如血管紧张素转换酶(ACE)抑制剂或β肾上腺素能受体阻滞剂。根据既定方案进行进一步的剂量调整。作为第五步也是最后一步,可以加用利尿剂。在这项针对高血压患者的大型跨国研究中,副作用相对较少。只有踝部水肿和咳嗽的发生率超过了0.5%(年轻患者中踝部水肿为1.3%,老年患者中为1.7%;年轻和老年患者中咳嗽均为0.5%)。两年后,所有患者中有84%仍在服用其基线治疗药物非洛地平。此处呈现的24个月数据表明,有可能实现HOT研究的主要目标。