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@article{1219888, author = {Václavík, Jan and Sedlák, Richard and Jarkovský, Jiří and Kociánová, Eva and Táborský, Miloš}, article_location = {Philadelphia}, article_number = {27}, doi = {http://dx.doi.org/10.1097/MD.0000000000000162}, keywords = {LOW-DOSE SPIRONOLACTONE; BLOOD-PRESSURE; REFRACTORY HYPERTENSION; PRIMARY ALDOSTERONISM; EUROPEAN-SOCIETY; EFFICACY; DENERVATION; EPLERENONE; PREVALENCE; ANTAGONISM}, language = {cze}, issn = {0025-7974}, journal = {Medicine}, title = {Effect of Spironolactone in Resistant Arterial Hypertension : A Randomized, Double-Blind, Placebo-Controlled Trial (ASPIRANT-EXT)}, volume = {93}, year = {2014} }
TY - JOUR ID - 1219888 AU - Václavík, Jan - Sedlák, Richard - Jarkovský, Jiří - Kociánová, Eva - Táborský, Miloš PY - 2014 TI - Effect of Spironolactone in Resistant Arterial Hypertension : A Randomized, Double-Blind, Placebo-Controlled Trial (ASPIRANT-EXT) JF - Medicine VL - 93 IS - 27 SP - "e162" EP - "e162" PB - Lippincott Williams & Wilkins SN - 00257974 KW - LOW-DOSE SPIRONOLACTONE KW - BLOOD-PRESSURE KW - REFRACTORY HYPERTENSION KW - PRIMARY ALDOSTERONISM KW - EUROPEAN-SOCIETY KW - EFFICACY KW - DENERVATION KW - EPLERENONE KW - PREVALENCE KW - ANTAGONISM N2 - This study was designed to assess the effect of the addition of low-dose spironolactone on blood pressure (BP) in patients with resistant arterial hypertension. Patients with office systolic blood pressure (SBP) >140 mm Hg or diastolic blood pressure (DBP) >90 mm Hg despite treatment with at least 3 antihypertensive drugs, including a diuretic, were enrolled in this double-blind, placebo-controlled, multicentre trial. One hundred sixty-one patients in outpatient internal medicine departments of 6 hospitals in the Czech Republic were randomly assigned to receive 25 mg of spironolactone (N = 81) or a placebo (N = 80) once daily as an add-on to their antihypertensive medication, using simple randomization. This study was registered with ClinicalTrials.gov, number NCT00524615. Analyses were done with 150 patients who finished the follow-up (74 in the spironolactone and 76 in the placebo group). At 8 weeks, BP values were decreased more by spironolactone, with differences in mean fall of SBP of -9.8, -13.0, -10.5, and -9.9 mm Hg (P < 0.001 for all) in daytime, nighttime, and 24-hour ambulatory BP monitoring and in the office. The respective DBP differences were -3.2, -6.4, -3.5, and -3.0 mm Hg (P < 0.013, P < 0.001, P = 0.005, and P = 0.003). Adverse events in both groups were comparable. The office SBP goal <140 mm Hg at 8 weeks was reached in 73% of patients using spironolactone and 41% using placebo (P = 0.001). Spironolactone in patients with resistant arterial hypertension leads to a significant decrease of both SBP and DBP and markedly improves BP control. ER -
VÁCLAVÍK, Jan, Richard SEDLÁK, Jiří JARKOVSKÝ, Eva KOCIÁNOVÁ a Miloš TÁBORSKÝ. Effect of Spironolactone in Resistant Arterial Hypertension : A Randomized, Double-Blind, Placebo-Controlled Trial (ASPIRANT-EXT). \textit{Medicine}. Philadelphia: Lippincott Williams \&{} Wilkins, 2014, roč.~93, č.~27, s.~''e162'', 9 s. ISSN~0025-7974. Dostupné z: https://dx.doi.org/10.1097/MD.0000000000000162.
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