Key result
Sildenafil linked to ~41% greater absolute three-year survival vs conventional therapy in idiopathic pulmonary arterial hypertension.
Why the study?
Does sildenafil therapy improve survival in patients with newly diagnosed idiopathic pulmonary arterial hypertension?
Cohort (n=77)
No
Does sildenafil therapy improve survival in patients with newly diagnosed idiopathic pulmonary arterial hypertension?
Absolute Event Rate: 68% vs 27%
p-value: p=<.001
Sildenafil therapy is associated with significantly improved long-term survival in patients with idiopathic pulmonary arterial hypertension compared to conventional therapy.
May support sildenafil consideration in idiopathic PAH; leaves open need for RCTs before practice change.
It has been reported that short-term sildenafil therapy is safe and effective for patients with pulmonary arterial hypertension. However, data regarding the impact of sildenafil on the survival of patients with idiopathic pulmonary arterial hypertension remain limited. The study was conducted on 77 patients with newly diagnosed idiopathic pulmonary arterial hypertension at Fu Wai Hospital between September 2005 and September 2009. Patients were divided into 2 groups: the sildenafil group and the conventional group. Nine patients treated with sildenafil were re-evaluated by right heart catheterization after 3 months. Our data demonstrated that the 6-minute walk distance, World Health Organization functional class, mixed venous oxygen saturation, and hemodynamics significantly improved after 3 months of sildenafil therapy (P < .05). The baseline characteristics of the sildenafil group were similar to those of the conventional group. The 1-, 2-, and 3-year survival rates in the sildenafil group were 88%, 72%, and 68% compared with 61%, 36%, and 27% in the conventional group (P < .001). The absence of sildenafil therapy, lower body mass index, and lower mixed venous oxygen saturation were found to be independent predictors of mortality. In conclusion, sildenafil therapy was found to be associated with improved survival in patients with idiopathic pulmonary arterial hypertension.
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Zeng et al. (2011) conducted a cohort in Idiopathic pulmonary arterial hypertension (n=77). Sildenafil therapy vs. Conventional therapy was evaluated on 3-year survival rate (p=<.001). Sildenafil therapy was associated with significantly higher 3-year survival compared to conventional therapy (68% vs 27%, P<0.001) in idiopathic pulmonary arterial hypertension.
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