Literature DB >> 18579234

Down patients with Eisenmenger syndrome: is bosentan treatment an option?

Mariëlle G J Duffels1, Jeroen C Vis, Rosa L E van Loon, Rolf M F Berger, Elke S Hoendermis, Arie P J van Dijk, Berto J Bouma, Barbara J M Mulder.   

Abstract

BACKGROUND: Favorable results of treatment with bosentan in patients with Eisenmenger syndrome are available. However, data in Down patients are lacking. In this study, we evaluate the therapeutic role of bosentan treatment in Down patients with Eisenmenger syndrome.
METHODS: In this open-label study, 24 Down patients (>18 years) with Eisenmenger syndrome (17 males) were treated with bosentan. Their mean age was 38 years (range 19-55 years). All Down patients were evaluated at baseline and during follow-up with laboratory tests, six-minute walk test (6-MWT), Doppler echocardiography, and quality of life questionnaires.
RESULTS: The median follow-up of Down patients treated with bosentan was 11.5 months (range 3-23 months). Induction of oral bosentan therapy was well tolerated among all 24 Down patients. Bosentan treatment was generally well tolerated. No serious adverse drug reactions were noted. Median 6-MWT increased from 296 m (range 40-424 m) to 325 m (range 84-459 m, p<0.05) after 12 weeks. After 26 and 52 weeks of treatment with bosentan, median 6-MWT distance was 276 m (range 140-462 m, n=15, p=0.6) and 287 m (range 131-409 m, n=7, p=0.3), respectively. Quality of life questionnaire scores remained stable during treatment.
CONCLUSION: Also patients with Down syndrome may benefit from bosentan treatment when they have Eisenmenger syndrome. Medical treatment appears to be safe and the treatment effects do not deviate from those observed in Eisenmenger patients without Down syndrome.

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Year:  2008        PMID: 18579234     DOI: 10.1016/j.ijcard.2008.02.025

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  14 in total

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2.  Adult patients with pulmonary arterial hypertension due to congenital heart disease: a review on advanced medical treatment with bosentan.

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Review 4.  Current challenges in pediatric pulmonary hypertension.

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7.  Adults with Down syndrome have reduced cardiac response after light exercise testing.

Authors:  J C Vis; H A C M De Bruin-Bon; B J Bouma; S A Huisman; L Imschoot; K van den Brink; B J M Mulder
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9.  Effect of bosentan on exercise capacity and clinical worsening in patients with dual down and eisenmenger syndrome.

Authors:  Giorgio Serino; Marco Guazzi; Angelo Micheletti; Carlo Lombardi; Rossella Danesi; Diana Negura; Mario Carminati; Massimo Chessa
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10.  Decrease in quality of life predicts mortality in adult patients with pulmonary arterial hypertension due to congenital heart disease.

Authors:  I M Blok; A C M J van Riel; M J Schuuring; M G Duffels; J C Vis; A P J van Dijk; E S Hoendermis; B J M Mulder; B J Bouma
Journal:  Neth Heart J       Date:  2015-05       Impact factor: 2.380

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