First experience with an oral combination therapy using bosentan and sildenafil for pulmonary arterial hypertension

被引:52
|
作者
Lunze, K.
Gilbert, N.
Mebus, S.
Miera, O.
Fehske, W.
Uhlemann, F.
Muehler, E. G.
Ewert, P.
Lange, P. E.
Berger, F.
Schulze-Neick, I.
机构
[1] Deutsch Herzzentrum Berlin, Klin Angeborene Herzfehler Kinderkardiol, D-13353 Berlin, Germany
[2] St Vincent Hosp, Abt Kardiol Innere Med, Cologne, Germany
[3] Olga Hosp, Abt Kinderkardiol, Stuttgart, Germany
[4] Univ Klinikum Aachen, Abt Padiatr Kardiol, Aachen, Germany
关键词
bosentan; combination; endothelin receptor antagonists; phosphodiesterase inhibitors; pulmonary arterial hypertension; sildenafil; congenital heart disease; children; competence network;
D O I
10.1111/j.1365-2362.2006.01692.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background New oral substances such as beraprost, bosentan and sildenafil have proven effective in different forms of pulmonary arterial hypertension (PAH), both alone and in combination with standard treatment such as intravenous and inhaled prostacyclins. However, there are few reports so far on the effect of a combination of exclusively oral substances. In this paper, we present our initial findings of treatment using a combination of these oral substances in a heterogeneous group of patients with different forms of PAH. Materials and methods Eleven patients with a median age of 12-9 years (5-5-54-7 years) with both idiopathic PAH and forms associated with congenital cardiac defects (PAH-CHD) with a mean pulmonary arterial pressure > 25 mmHg were enrolled in an observational, open-label, prospective, single-centre study. Either combination treatment with bosentan and sildenafil was started initially, or an existing bosentan treatment was complemented with siIdenafil given as an add-on therapy. Mean doses given were 2-3 +/- 0-6 mg kg(-1) for bosentan and 2.1 +/- 0.9 mg kg(-1) for sildenafil. Clinical status, exercise capacity and haemodynamics were assessed at baseline and at the end of the observation period after a mean follow-up time of 1.1 years (0.5 - 2.5 years). Results No major side effects regarding liver function and blood pressure regulation were noted. One patient died of sudden death elsewhere. Most patients were in Newyork Heart Association (NYHA) functional class III. Clinical improvement was about one NYHA class (mean 2-8 +/- 0-4-1-6 +/- 0-8, P=0-001), which was associated with an increase of transcutaneous oxygen saturation (89-9 +/- 9-9-92-3 +/- 7-1%;P=0-037), maximum oxygen uptake (18-1 +/- 6-8-22.8 +/- 10.4 mL kg(-1) * min-, P = 0-043), and 6-minute walking distance (351 58-451 119 m; P = 0-039). Mean pulmonary arterial pressure measured invasively decreased (62 +/- 12-46 18 mmHg; P = 0-041). Conclusions In our patient group, a combination of oral bosentan and sildenafil proved to be safe and effective. Clearly, randomized, double-blind, placebo-controlled studies are warranted to define the role and type of combination therapies in PAH.
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收藏
页码:32 / 38
页数:7
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