Addition of Spironolactone in Patients With Resistant Arterial Hypertension (ASPIRANT) A Randomized, Double-Blind, Placebo-Controlled Trial

被引:254
作者
Vaclavik, Jan [1 ,2 ]
Sedlak, Richard [3 ]
Plachy, Martin [4 ]
Navratil, Karel [5 ]
Plasek, Jiri [6 ]
Jarkovsky, Jiri [7 ,8 ]
Vaclavik, Tomas [9 ]
Husar, Roman [10 ]
Kocianova, Eva [1 ,2 ]
Taborsky, Milos [1 ,2 ]
机构
[1] Univ Hosp Olomouc, Dept Internal Med 1, Olomouc 77520, Czech Republic
[2] Palacky Univ, Sch Med, Olomouc 77520, Czech Republic
[3] Prostejov Hosp, Dept Internal Med, Prostejov, Czech Republic
[4] St Annes Univ Hosp, Dept Internal Med 2, Brno, Czech Republic
[5] Mil Hosp, Dept Internal Med, Olomouc, Czech Republic
[6] Univ Ostrava, Univ Hosp Ostrava, Dept Internal Med, Ostrava, Czech Republic
[7] Masaryk Univ, Fac Med, Inst Biostati & Anal, Brno, Czech Republic
[8] Masaryk Univ, Fac Sci, Brno, Czech Republic
[9] Univ Econ Prague, Fac Informat & Stat, Dept Stat & Probabil, Prague, Czech Republic
[10] Hranice Hosp, Dept Internal Med, Hranice Na Morave, Czech Republic
关键词
resistant hypertension; spironolactone; clinical trials; blood pressure; ambulatory blood pressure monitoring; LOW-DOSE SPIRONOLACTONE; BLOOD-PRESSURE; PULSE PRESSURE; ALDOSTERONE ANTAGONIST; EUROPEAN-SOCIETY; RENIN RATIO; EFFICACY; RISK; MANAGEMENT; DIAGNOSIS;
D O I
10.1161/HYPERTENSIONAHA.111.169961
中图分类号
R6 [外科学];
学科分类号
100210 [外科学];
摘要
There is currently limited data on which drug should be used to improve blood pressure (BP) control in patients with resistant hypertension. This study was designed to assess the effect of the addition of 25 mg of spironolactone on BP in patients with resistant arterial hypertension. Patients with office systolic BP > 140 mm Hg or diastolic BP > 90 mm Hg despite treatment with at least 3 antihypertensive drugs, including a diuretic, were enrolled in this double-blind, placebo-controlled, multicenter trial. One hundred seventeen patients were randomly assigned to receive spironolactone (n = 59) or a placebo (n = 58) as an add-on to their antihypertensive medication, by the method of simple randomization. Analyses were done with 111 patients (55 in the spironolactone and 56 in the placebo groups). At 8 weeks, the primary end points, a difference in mean fall of BP on daytime ambulatory BP monitoring (ABPM), between the groups was -5.4 mm Hg (95% CI -10.0; -0.8) for systolic BP (P = 0.024) and -1.0 mm Hg (95% CI -4.0; 2.0) for diastolic BP (P = 0.358). The APBM nighttime systolic, 24-hour ABPM systolic, and office systolic BP values were significantly decreased by spironolactone (difference of -8.6, -9.8, and -6.5 mm Hg; P = 0.011, 0.004, and 0.011), whereas the fall of the respective diastolic BP values was not significant (-3.0, -1.0, and -2.5 mm Hg; P = 0.079, 0.405, and 0.079). The adverse events in both groups were comparable. In conclusion, spironolactone is an effective drug for lowering systolic BP in patients with resistant arterial hypertension. (Hypertension. 2011;57:1069-1075.). Online Data Supplement
引用
收藏
页码:1069 / U94
页数:9
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