Literature DB >> 16831475

The effect of beta-blocker therapy on clinical outcome in patients with Marfan's syndrome: a meta-analysis.

Deborah R Gersony1, Mary Ann McClaughlin, Zhezhen Jin, Welton M Gersony.   

Abstract

OBJECTIVE: To assess the effect of beta-blockade therapy on clinical outcome in patients with Marfan's syndrome.
BACKGROUND: Despite the lack of definitive evidence to support its efficacy, beta-blocker therapy is widely used prophylactically in patients with Marfan's syndrome.
METHODS: A meta-analysis was instituted, which included studies identified by a systematic review of MEDLINE of peer-reviewed publications and by abstracts from annual scientific meeting. Outcome measures of mortality and major morbidity were compared between patients treated and untreated with beta-blockade therapy. Data was combined according to both a fixed-effects and random-effects model. The endpoints included aortic dissection or rupture, cardiovascular surgery, or death.
RESULTS: Six studies were included, 5 were non-randomized follow-up studies and 1 was a prospective randomized trial (802 patients). Ninety-six of 433 patients treated with beta-blocker therapy and 74 of 369 untreated patients reached designated endpoints. Utilizing a fixed-effects model, patients treated with beta-blocker therapy were more likely to reach an endpoint (odds ratio=1.50 with 95% CI 1.05-2.16). However, by a random-effects model, the treatment effect failed to reach significance (1.54 with 95% CI 0.99-2.40).
CONCLUSIONS: On the basis of this meta-analysis, there is no evidence that beta-blockade therapy has clinical benefit in patients with Marfan's syndrome.

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Year:  2006        PMID: 16831475     DOI: 10.1016/j.ijcard.2005.11.116

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


  28 in total

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Authors:  Jeffrey A Jones; John S Ikonomidis
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Review 2.  Aortic Involvement in Pediatric Marfan syndrome: A Review.

Authors:  Omonigho Ekhomu; Zahra J Naheed
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Review 4.  Preventing the aortic complications of Marfan syndrome: a case-example of translational genomic medicine.

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Review 5.  Aetiology and management of hereditary aortopathy.

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6.  Strategies to prevent aortic complications in Marfan syndrome.

Authors:  Lucio Sartor; Alberto Forteza
Journal:  J Thorac Dis       Date:  2017-05       Impact factor: 2.895

Review 7.  Molecular pathogenesis of genetic and sporadic aortic aneurysms and dissections.

Authors:  Ying H Shen; Scott A LeMaire
Journal:  Curr Probl Surg       Date:  2017-02-03       Impact factor: 1.909

8.  Medical management of aortic disease in Marfan syndrome.

Authors:  Syed Usman Bin Mahmood; Camilo A Velasquez; Mohammad A Zafar; Ayman A Saeyeldin; Adam J Brownstein; Bulat A Ziganshin; John A Elefteriades; Sandip K Mukherjee
Journal:  Ann Cardiothorac Surg       Date:  2017-11

9.  Abnormal Longitudinal Growth of the Aorta in Children with Familial Bicuspid Aortic Valve.

Authors:  Holly Nadorlik; Jessica L Bowman; Sara Fitzgerald-Butt; May Ling Mah; Kim L McBride; John P Kovalchin; Vidu Garg
Journal:  Pediatr Cardiol       Date:  2017-09-25       Impact factor: 1.655

10.  Role of beta-blockers in Marfan's syndrome and bicuspid aortic valve: A time for re-appraisal.

Authors:  Balu Vaidyanathan
Journal:  Ann Pediatr Cardiol       Date:  2008-07
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