TY - JOUR
T1 - Sildenafil in Heart Failure (SilHF). An investigator-initiated multinational randomized controlled clinical trial
T2 - Rationale and design
AU - Cooper, Trond J.
AU - Guazzi, Marco
AU - Al-Mohammad, Abdallah
AU - Amir, Offer
AU - Bengal, Tuvia
AU - Cleland, John G.
AU - Dickstein, Kenneth
PY - 2013/1
Y1 - 2013/1
N2 - Aims: Heart failure (HF) is a major clinical problem and, despite advances in both pharmacological and device therapy, the mortality remains high and quality of life poor. Over the last decade there has been growing interest in using phosphodiesterase-5 (PDE-5) inhibitors in HF associated with group 2 pulmonary hypertension (PH), with benefits reported on pulmonary haemodynamic and functional status in single-centre trialsMethodsThe Sildenafil in Heart Failure (SilHF) trial is a randomized, placebo-controlled multinational trial designed to assess efficacy and tolerability of PDE-5 inhibition with sildenafil (target dose 40 mg three times per day) in 210 patients with HF, New York Heart Association (NYHA) functional class II or III, and evidence of group 2 PH. The co-primary endpoints are patient global assessment and the 6 min walk test. Secondary endpoints include NYHA functional class and the quality of life tools Euro QoL 5D and the Kansas City questionnaire. Patients will be followed up for 6 months.PerspectiveThe authors hypothesize that PDE-5 inhibition can improve exercise capacity and symptoms with acceptable tolerability in patients with HF and group 2 PH
AB - Aims: Heart failure (HF) is a major clinical problem and, despite advances in both pharmacological and device therapy, the mortality remains high and quality of life poor. Over the last decade there has been growing interest in using phosphodiesterase-5 (PDE-5) inhibitors in HF associated with group 2 pulmonary hypertension (PH), with benefits reported on pulmonary haemodynamic and functional status in single-centre trialsMethodsThe Sildenafil in Heart Failure (SilHF) trial is a randomized, placebo-controlled multinational trial designed to assess efficacy and tolerability of PDE-5 inhibition with sildenafil (target dose 40 mg three times per day) in 210 patients with HF, New York Heart Association (NYHA) functional class II or III, and evidence of group 2 PH. The co-primary endpoints are patient global assessment and the 6 min walk test. Secondary endpoints include NYHA functional class and the quality of life tools Euro QoL 5D and the Kansas City questionnaire. Patients will be followed up for 6 months.PerspectiveThe authors hypothesize that PDE-5 inhibition can improve exercise capacity and symptoms with acceptable tolerability in patients with HF and group 2 PH
KW - Heart failure
KW - Pulmonary hypertension
KW - Quality of life tools
KW - Sildenafil
KW - Symptoms
UR - http://www.scopus.com/inward/record.url?scp=84871220360&partnerID=8YFLogxK
U2 - 10.1093/eurjhf/hfs152
DO - 10.1093/eurjhf/hfs152
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C2 - 23097067
AN - SCOPUS:84871220360
SN - 1388-9842
VL - 15
SP - 119
EP - 122
JO - European Journal of Heart Failure
JF - European Journal of Heart Failure
IS - 1
ER -