Widimský Jiří
Vnitr Lek. 2015 Dec;61(12):1067-71.
The PATHWAY-2 study, funded by the British Heart Foundation, randomised 335 patients with resistant hypertension (already treated according to guidelines) to sequentially receive 12 weeks of spironolactone (25-50 mg), bisoprolol (5-10 mg), doxazosin (4-8 mg modified release) and placebo. The study design allowed drug comparisons in each patient, with 230 patients completing all cycles. Results showed that spironolactone reduced home systolic BP by 8.70 mm Hg more than placebo (<0.001), 4.26 mmHg more than bisoprolol/doxazosin (<0.001), 4.03 mm Hg more than doxazosin (<0.001), and by 4.48 mm Hg more than bisoprolol. By the end of the trial, there would only be 15 patients considered eligible for renal denervation trials in uncontrolled hypertension. PATHWAY-2 will have significant implications for patient recruitment in to other trials.
由英国心脏基金会资助的PATHWAY - 2研究,将335例顽固性高血压患者(已按指南进行治疗)随机分组,依次接受12周的螺内酯(25 - 50毫克)、比索洛尔(5 - 10毫克)、多沙唑嗪(4 - 8毫克缓释制剂)和安慰剂治疗。该研究设计允许对每位患者使用的药物进行比较,有230例患者完成了所有周期。结果显示,与安慰剂相比,螺内酯使家庭收缩压降低了8.70毫米汞柱(<0.001),比索洛尔/多沙唑嗪降低了4.26毫米汞柱(<0.001),比多沙唑嗪降低了4.03毫米汞柱(<0.001),比索洛尔降低了4.48毫米汞柱。到试验结束时,在未控制的高血压患者中,只有15例被认为符合肾脏去神经支配试验的条件。PATHWAY - 2研究将对其他试验的患者招募产生重大影响。