Literature DB >> 35902413

Pediatric Heart Network Trial of Losartan vs. Atenolol in Children and Young Adults with Marfan Syndrome: Impact on Prescription Practices.

Dwight M Robertson1,2, Dongngan T Truong3, Daniel A Cox3, Harris L Carmichael4, Zhining Ou5, L LuAnn Minich3, Richard V Williams3, E Seda Selamet Tierney6.   

Abstract

The Pediatric Heart Network (PHN) trial showed similar efficacy of β-blockers (BB) and angiotensin receptor blockers (ARB) for aortic root dilation in Marfan syndrome, but the impact on prescription practices is unknown. We hypothesized BB and ARB prescriptions would increase after the trial results were published (2014). Prescription data (2007-2016) were obtained from outpatient encounters (IBM Marketscan) for Marfan syndrome patients (6 months-25 years old). Excluding 2014 as a washout period, we analyzed two intervals: 2007-2013 and 2015-2016. Medication categories included BB, ARB, angiotensin converting enzyme inhibitors (ACEI), combination (BB/ARB and/or BB/ACEI), and no drug. Interrupted time-series analysis assessed immediate level change after publication and change in slope for the trend pre- and post-publication. Odds ratios (OR) and 95% confidence intervals from logistic regressions and generalized estimating equation methods accounted for correlation of prescriptions within patients. In 1499 patients (age 14.1 ± 6.1 years, 59% female) seen 2007-2013, BB trended lower [OR 0.91 (0.89, 0.93), p < 0.001] and ARB trended higher [OR 1.12 (1.07, 1.18), p < 0.001], while combination, ACEI, and no drug remained stable. This trend persisted, but was not significant, for BB [OR 0.54 (0.27, 1.08), p = 0.37] and ARB [OR 1.91 (0.55, 6.69), p = 0.31] in 2015-2016. Combination, ACEI, and no drug remained similar. In short term follow-up, changes in prescription practices following publication of the PHN trial were not statistically significant. This may be due to a change seen prior to publication with early adoption of ARBs that was maintained after confirmation of their effectiveness.
© 2022. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.

Entities:  

Keywords:  Aortic dissection; Aortic root dilation; Congenital heart disease; Marfan syndrome

Year:  2022        PMID: 35902413     DOI: 10.1007/s00246-022-02976-z

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.838


  20 in total

Review 1.  Treatment of aortic disease in patients with Marfan syndrome.

Authors:  Dianna M Milewicz; Harry C Dietz; D Craig Miller
Journal:  Circulation       Date:  2005-03-22       Impact factor: 29.690

2.  Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene.

Authors:  H C Dietz; G R Cutting; R E Pyeritz; C L Maslen; L Y Sakai; G M Corson; E G Puffenberger; A Hamosh; E J Nanthakumar; S M Curristin
Journal:  Nature       Date:  1991-07-25       Impact factor: 49.962

Review 3.  Diffusion theory and knowledge dissemination, utilization, and integration in public health.

Authors:  Lawrence W Green; Judith M Ottoson; César García; Robert A Hiatt
Journal:  Annu Rev Public Health       Date:  2009       Impact factor: 21.981

Review 4.  A systematic review of the pharmacological management of aortic root dilation in Marfan syndrome.

Authors:  Varsha Thakur; Kathryn N Rankin; Lisa Hartling; Andrew S Mackie
Journal:  Cardiol Young       Date:  2012-10-19       Impact factor: 1.093

Review 5.  The Marfan syndrome.

Authors:  R E Pyeritz
Journal:  Annu Rev Med       Date:  2000       Impact factor: 13.739

6.  Atenolol versus losartan in children and young adults with Marfan's syndrome.

Authors:  Ronald V Lacro; Harry C Dietz; Lynn A Sleeper; Anji T Yetman; Timothy J Bradley; Steven D Colan; Gail D Pearson; E Seda Selamet Tierney; Jami C Levine; Andrew M Atz; D Woodrow Benson; Alan C Braverman; Shan Chen; Julie De Backer; Bruce D Gelb; Paul D Grossfeld; Gloria L Klein; Wyman W Lai; Aimee Liou; Bart L Loeys; Larry W Markham; Aaron K Olson; Stephen M Paridon; Victoria L Pemberton; Mary Ella Pierpont; Reed E Pyeritz; Elizabeth Radojewski; Mary J Roman; Angela M Sharkey; Mario P Stylianou; Stephanie Burns Wechsler; Luciana T Young; Lynn Mahony
Journal:  N Engl J Med       Date:  2014-11-18       Impact factor: 91.245

7.  Progression of aortic dilatation and the benefit of long-term beta-adrenergic blockade in Marfan's syndrome.

Authors:  J Shores; K R Berger; E A Murphy; R E Pyeritz
Journal:  N Engl J Med       Date:  1994-05-12       Impact factor: 91.245

8.  Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome.

Authors:  Jennifer P Habashi; Daniel P Judge; Tammy M Holm; Ronald D Cohn; Bart L Loeys; Timothy K Cooper; Loretha Myers; Erin C Klein; Guosheng Liu; Carla Calvi; Megan Podowski; Enid R Neptune; Marc K Halushka; Djahida Bedja; Kathleen Gabrielson; Daniel B Rifkin; Luca Carta; Francesco Ramirez; David L Huso; Harry C Dietz
Journal:  Science       Date:  2006-04-07       Impact factor: 47.728

9.  Angiotensin II blockade and aortic-root dilation in Marfan's syndrome.

Authors:  Benjamin S Brooke; Jennifer P Habashi; Daniel P Judge; Nishant Patel; Bart Loeys; Harry C Dietz
Journal:  N Engl J Med       Date:  2008-06-26       Impact factor: 91.245

10.  TGF-beta in the pathogenesis and prevention of disease: a matter of aneurysmic proportions.

Authors:  Harry C Dietz
Journal:  J Clin Invest       Date:  2010-01-25       Impact factor: 14.808

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