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

被引:52
作者
Duffels, Marielle G. J. [1 ]
Vis, Jeroen C. [1 ]
van Loon, Rosa L. E. [2 ]
Berger, Rolf M. F. [2 ]
Hoendermis, Elke S. [3 ]
van Dijk, Arie P. J. [4 ]
Bouma, Berto J. [1 ]
Mulder, Barbara J. M. [1 ,5 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Cardiol, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Paediat Cardiol, Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Cardiol, Groningen, Netherlands
[4] Univ Med Ctr Nijmegen, Dept Cardiol, Nijmegen, Netherlands
[5] Univ Med Ctr Utrecht, Dept Cardiol, Utrecht, Netherlands
关键词
Down syndrome; Congenital heart disease; Eisenmenger syndrome; Pulmonary arterial hypertension; Bosentan treatment; PULMONARY ARTERIAL-HYPERTENSION; CONGENITAL HEART-DISEASE; QUALITY-OF-LIFE; VASCULAR-DISEASE; ADULTS; VALIDATION; CHILDREN; DEFECTS; THERAPY;
D O I
10.1016/j.ijcard.2008.02.025
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:378 / 383
页数:6
相关论文
共 26 条
[1]   Translation, validation, and norming of the Dutch language version of the SF-36 Health Survey in community and chronic disease populations [J].
Aaronson, NK ;
Muller, M ;
Cohen, PDA ;
Essink-Bot, ML ;
Fekkes, M ;
Sanderman, R ;
Sprangers, MAG ;
Velde, AT ;
Verrips, E .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1998, 51 (11) :1055-1068
[2]   Long-term oral bosentan treatment in patients with pulmonary arterial hypertension related to congenital heart disease: a 2-year study [J].
Apostolopoulou, S. C. ;
Manginas, A. ;
Cokkinos, D. V. ;
Rammos, S. .
HEART, 2007, 93 (03) :350-354
[3]   Possibilities and impossibilities in the evaluation of pulmonary vascular disease in congenital heart defects [J].
Berger, RMF .
EUROPEAN HEART JOURNAL, 2000, 21 (01) :17-27
[4]  
Bouzas B, 2005, REV ESP CARDIOL, V58, P465, DOI 10.1157/13074838
[5]   Measurement of quality of life in pulmonary hypertension and its significance [J].
Cenedese, E. ;
Speich, R. ;
Dorschner, L. ;
Ulrich, S. ;
Maggiorini, M. ;
Jenni, R. ;
Fischler, M. .
EUROPEAN RESPIRATORY JOURNAL, 2006, 28 (04) :808-815
[6]   Initial experience with Bosentan therapy in patients with the Eisenmenger syndrome [J].
Christensen, DD ;
McConnell, ME ;
Book, WM ;
Mahle, WT .
AMERICAN JOURNAL OF CARDIOLOGY, 2004, 94 (02) :261-263
[7]   Comparison and validation of three measures of quality of life in patients with pulmonary hypertension [J].
Chua, R. ;
Keogh, A. M. ;
Byth, K. ;
O'Loughlin, A. .
INTERNAL MEDICINE JOURNAL, 2006, 36 (11) :705-710
[8]   ATS statement: Guidelines for the six-minute walk test [J].
Crapo, RO ;
Casaburi, R ;
Coates, AL ;
Enright, PL ;
MacIntyre, NR ;
McKay, RT ;
Johnson, D ;
Wanger, JS ;
Zeballos, RJ ;
Bittner, V ;
Mottram, C .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (01) :111-117
[9]   Eisenmenger syndrome - Factors relating to deterioration and death [J].
Daliento, L ;
Somerville, J ;
Presbitero, P ;
Menti, L ;
Brach-Prevert, S ;
Rizzoli, G ;
Stone, S .
EUROPEAN HEART JOURNAL, 1998, 19 (12) :1845-1855
[10]   Exercise intolerance in adult congenital heart disease - Comparative severity, correlates, and prognostic implication [J].
Diller, GP ;
Dimopoulos, K ;
Okonko, D ;
Li, W ;
Babu-Narayan, SV ;
Broberg, CS ;
Johansson, B ;
Bouzas, B ;
Mullen, MJ ;
Poole-Wilson, PA ;
Francis, DP ;
Gatzoulis, MA .
CIRCULATION, 2005, 112 (06) :828-835