Treatment of thromboangiitis obliterans (Buerger's disease) with bosentan

BMC Cardiovascular Disorders

Research Article

Silvia Bleda¹  Francisco Acin¹  Cesar Varela¹  Joaquin De Haro¹  Leticia Esparza¹ 

[1] Department of Angiology and Vascular Surgery, Hospital Universitario de Getafe, Madrid, Spain;

关键词: Bosentan;    Iloprost;    Major Amputation;    Ischaemic Lesion;    Lumbar Sympathectomy;   

DOI  :  10.1186/1471-2261-12-5

 received in 2011-08-01, accepted in 2012-02-14,  发布年份 2012

来源: Springer

【 摘 要 】

BackgroundThis study assessed the effectiveness and safety of bosentan when administered to thromboangiitis obliterans (Buerger's disease) patients.MethodsA clinical pilot study was designed in which patients with ulcer and/or pain at rest were treated with bosentan p.o. at a dose of 62.5 mg twice daily during the first month, which was thereafter up-titrated to 125 mg twice daily. The study endpoints were clinical improvement rate, major or minor amputation rate, haemodynamic changes, changes in endothelial function and angiographic changes.ResultsSeven out of 12 patients were male (58%). Median age was 39 years (range 29-49). The median follow-up was 20 months (range 11-40). All patients were smokers. With bosentan treatment, new ischaemic lesions were observed in only one patient. Overall, clinical improvement was observed in 12 of the 13 extremities (92%). Only two out of 13 extremities underwent amputation (one major and one minor) after bosentan treatment. After being assessed by digital arteriography with subtraction or angio-magnetic resonance imaging, an increase of distal flow was observed in 10 out of the 12 patients. All patients experienced a statistically significant improvement in their BAFMD values (mean: 1.8 at baseline; 6.6 at the end of the treatment; 12.7 three months after the end of the treatment; p < 0.01).ConclusionBosentan treatment may result in an improvement of clinical, angiographic and endothelial function outcomes. Bosentan should be investigated further in the management of TAO patients. Larger studies are required to confirm these results.Trial RegistrationClinicalTrials.gov: NCT01447550

【 授权许可】

CC BY   
© De Haro et al; licensee BioMed Central Ltd. 2012