VACLAVIK, Jan, Richard SEDLAK, Jiří JARKOVSKÝ, Eva KOCIANOVA a Milos TABORSKY. The effect of spironolactone in patients with resistant arterial hypertension in relation to baseline blood pressure and secondary causes of hypertension. Biomedical Papers, Olomouc: Palacky University. Olomouc: Palacky University, 2013, roč. 157, č. 1, s. 50-55. ISSN 1213-8118. Dostupné z: https://dx.doi.org/10.5507/bp.2012.078.
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Základní údaje
Originální název The effect of spironolactone in patients with resistant arterial hypertension in relation to baseline blood pressure and secondary causes of hypertension
Autoři VACLAVIK, Jan (203 Česká republika), Richard SEDLAK (203 Česká republika), Jiří JARKOVSKÝ (203 Česká republika, garant, domácí), Eva KOCIANOVA (203 Česká republika) a Milos TABORSKY (203 Česká republika).
Vydání Biomedical Papers, Olomouc: Palacky University, Olomouc, Palacky University, 2013, 1213-8118.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30000 3. Medical and Health Sciences
Stát vydavatele Česká republika
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 1.661
Kód RIV RIV/00216224:14110/13:00072692
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.5507/bp.2012.078
UT WoS 000316989100009
Klíčová slova anglicky resistant hypertension; spironolactone; clinical trials; blood pressure; secondary hypertension
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Ing. Mgr. Věra Pospíšilíková, učo 9005. Změněno: 19. 3. 2014 11:27.
Anotace
Aims. There are currently limited data about whether the effect of spironolactone in patients with resistant arterial hypertension depends on baseline blood pressure and the presence of a secondary cause of hypertension. Methods. Patients with office systolic blood pressure (BP) > 140 mmHg or diastolic BP > 90 mmHg, despite treatment with at least 3 antihypertensive drugs including a diuretic, were randomly assigned to receive spironolactone or a placebo for 8 weeks in a double-blind, placebo-controlled, multicentre trial (ASPIRANT). Results. Analyses were done with 55 patients treated with spironolactone. The degree of BP reduction after 8 weeks of spironolactone treatment did not differ significantly between the three tertiles of baseline systolic BP and patients with and without a secondary cause of hypertension. The reduction of office systolic, office diastolic BP and office pulse pressure was significantly lower in the highest tertile with baseline diastolic BP > 97 mmHg. Conclusions. Spironolactone treatment is effective to a similar extent both in patients with and without a secondary cause of hypertension and regardless of the baseline value of systolic BP. Less effect of spironolactone was found in patients with the highest baseline diastolic BP.
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