Mallion J M, Pehrsson N G, Raveau-Landon C, Boutelant S, Ménard J
Service de médecine interne et cardiologie, centre hospitalier universitaire de Grenoble.
Arch Mal Coeur Vaiss. 1996 Aug;89(8):1093-6.
International, prospective, randomized HOT study aims to determine the optimal BP level under treatment in order to reduce at the most the cardiovascular morbidity/mortality. Defined by randomization, the level to obtain is DBP < or = 80, 85, 90 mmHg. The treatment is started by felodipine 5 mg/day then, if necessary, a bitherapy is prescribed and then, if necessary, a tritherapy. 19,193 patients have been included (BP at randomization 170 +/- 15/105 +/- 4 mmHg). After 1 year treatment, it is possible to search for the influence on the clinical tolerance of sex, age, BP goal, geographic area, time and treatment. The percentage of patients with side effects by BP goals and by treatment type are, during the time and in different geographic areas, the following (NE/Northern Europe = Norway, Switzerland, Belgium, Hungary, Sweden, Denmark, Finland, The Netherlands, UK, Germany, Austria; SE/Southern Europe = Italy, Spain, Greece): [table: see text] The target BP and age don't nearly influence the clinical tolerance. The side effects reported by the physicians are more numerous at the treatment start than at longeur terme. That is due to the therapeutic modifications of the physicians or to a better acceptation of the drugs by the patients or to a real disappearance of the side effects. Reported side effects are more frequent in Southern Europe, France than Northern Europe and more frequent among women that men. The incidence of side effects is proportional to the number of prescribed drugs. Time and the number of antihypertensive drugs appear as the most important factors.
国际前瞻性随机 HOT 研究旨在确定治疗中的最佳血压水平,以最大程度降低心血管发病率/死亡率。通过随机分组确定的目标血压水平为舒张压≤80、85、90 mmHg。治疗起始使用非洛地平 5 毫克/天,必要时联合两种药物治疗,如有需要则采用三联疗法。共纳入 19193 例患者(随机分组时血压为 170±15/105±4 mmHg)。经过 1 年治疗后,可探究性别、年龄、血压目标、地理区域、时间和治疗方法对临床耐受性的影响。在不同时间和不同地理区域,按血压目标和治疗类型划分的出现副作用的患者百分比情况如下(NE/北欧=挪威、瑞士、比利时、匈牙利、瑞典、丹麦、芬兰、荷兰、英国、德国、奥地利;SE/南欧=意大利、西班牙、希腊):[表格:见原文]目标血压和年龄对临床耐受性几乎没有影响。医生报告的副作用在治疗开始时比长期治疗时更多。这是由于医生调整治疗方案、患者对药物的接受度提高或副作用实际消失。在南欧、法国报告的副作用比北欧更常见,女性比男性更频繁。副作用的发生率与所开药物数量成正比。时间和抗高血压药物数量似乎是最重要的因素。