Okpechi I G, Schoeman H S, Longo-Mbenza B, Oke D A, Kingue S, Nkoua J L, Rayner B L
Division of Nephrology and Hypertension, Groote Schuur Hospital, University of Cape Town, South Africa.
Cardiovasc J Afr. 2011 Mar-Apr;22(2):79-84. doi: 10.5830/cvja-2010-086.
Hypertension is a common cardiovascular disease, affecting adults worldwide and it accounts for up to 30% of all deaths. The need for better control of arterial hypertension justifies observational studies designed to better understand the real-life management of hypertensive patients. The ASTRAL study was primarily designed to evaluate the percentage of hypertensive patients achieving blood pressure goals after eight weeks of treatment with a fixeddose combination of ramipril/hydrochlorothiazide (HCTZ).
The study was a multi-centre, non-comparative, Open-label, observational study conducted in 36 centres in five sub-Saharan African countries, namely Cameroon, Congo Brazzaville, Democratic Republic of Congo (DRC), Madagascar and Nigeria. Four hundred and forty-nine men and women 18 years of age or older with hypertension not controlled by an ACE inhibitor, a diuretic or any other monotherapy or anti-hypertensive combination not containing a diuretic in a fixed dose were considered eligible for inclusion in this eight-week study. The study consisted of three visits, visit one (V1) at baseline, visit two (V2) after four weeks and visit three (V3) after eight weeks.
The mean age of the patients was 54.7 ± 11.7 years (20-90 years) and most were categorised by the WHO criteria as either overweight or obese (71.6%). After four and eight weeks of treatment with the study drug, systolic and diastolic blood pressures significantly changed from baseline: -24.7/-14.2 mmHg (p < 0.001) and -31.7/-17.9 mmHg (p < 0.001), respectively. There were 60.2% of the non-diabetics on prior monotherapy who, at eight weeks, fulfilled the primary blood pressure goal for SBP and DBP, versus 26.5% of the diabetic patients, also on monotherapy. Few adverse events were reported, with facial oedema and dry cough recurring twice in two patients.
Fixed-dose combination of ramipril/HCTZ is therefore effective, tolerable and has a good safety profile for blood pressure control in black Africans.
高血压是一种常见的心血管疾病,影响着全球成年人,占所有死亡人数的30%。更好地控制动脉高血压的需求促使开展观察性研究,以更好地了解高血压患者的实际治疗情况。ASTRAL研究主要旨在评估使用雷米普利/氢氯噻嗪(HCTZ)固定剂量联合治疗八周后达到血压目标的高血压患者百分比。
该研究是一项多中心、非对比、开放标签的观察性研究,在撒哈拉以南非洲五个国家的36个中心进行,这五个国家分别是喀麦隆、刚果布拉柴维尔、刚果民主共和国、马达加斯加和尼日利亚。449名18岁及以上的男性和女性高血压患者,若其高血压未被ACE抑制剂、利尿剂或任何其他单一疗法或不含固定剂量利尿剂的抗高血压联合疗法控制,则被认为有资格纳入这项为期八周的研究。该研究包括三次访视,第一次访视(V1)在基线期,第二次访视(V2)在四周后,第三次访视(V3)在八周后。
患者的平均年龄为54.7±11.7岁(20 - 90岁),大多数患者根据世界卫生组织标准被归类为超重或肥胖(71.6%)。使用研究药物治疗四周和八周后,收缩压和舒张压与基线相比有显著变化:分别为-24.7/-14.2 mmHg(p < 0.001)和-31.7/-17.9 mmHg(p < 0.001)。在八周时,之前接受单一疗法的非糖尿病患者中有60.2%达到了收缩压和舒张压的主要血压目标,而同样接受单一疗法的糖尿病患者这一比例为26.5%。报告的不良事件很少,两名患者出现两次面部水肿和干咳。
因此,雷米普利/氢氯噻嗪固定剂量联合疗法对黑人非洲人的血压控制有效、耐受性良好且安全性高。