Literature DB >> 22104675

Long-term implications of emergency versus elective proximal aortic surgery in patients with Marfan syndrome in the Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions Consortium Registry.

Howard K Song1, Mark Kindem, Joseph E Bavaria, Harry C Dietz, Dianna M Milewicz, Richard B Devereux, Kim A Eagle, Cheryl L Maslen, Barbara L Kroner, Reed E Pyeritz, Kathryn W Holmes, Jonathan W Weinsaft, Victor Menashe, William Ravekes, Scott A LeMaire.   

Abstract

OBJECTIVE: Patients with Marfan syndrome with aortic root aneurysms undergo elective aortic root replacement to avoid the life-threatening outcomes of aortic dissection and emergency repair. The long-term implications of failed aortic surveillance leading to acute dissection and emergency repair are poorly defined. We compared the long-term clinical courses of patients with Marfan syndrome who survive emergency versus elective proximal aortic surgery.
METHODS: The Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions Registry is a National Institutes of Health-funded multicenter database and biorepository that enrolls patients with genetically triggered thoracic aortic aneurysms. Of the 635 patients with Marfan syndrome enrolled as of March 2011, 194 had undergone proximal aortic replacement. Patients were grouped according to emergency (n = 47) or elective (n = 147) status at the time of surgery.
RESULTS: Patients in the emergency group were more likely to have incomplete proximal aortic resection; 83% of emergency procedures included aortic root replacement, compared with 95% of elective procedures. At long-term follow-up (mean, >6 years), the emergency group had a higher incidence of chronic dissection of the distal aorta and significantly larger diameters in distal aortic segments than elective patients. Patients in the emergency group had undergone more operations (1.31 vs 1.11 procedures/patient; P = .01) and had lower activity scores on a health-related quality of life survey.
CONCLUSIONS: For patients with Marfan syndrome, failed aortic surveillance and consequent emergency dissection repair have important long-term implications with regard to the status of the distal aorta, need for multiple procedures, and quality of life. These findings emphasize the importance of aortic surveillance and timely elective aortic root aneurysm repair for patients with Marfan syndrome.
Copyright © 2012 The American Association for Thoracic Surgery. All rights reserved.

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Year:  2011        PMID: 22104675      PMCID: PMC3260411          DOI: 10.1016/j.jtcvs.2011.10.024

Source DB:  PubMed          Journal:  J Thorac Cardiovasc Surg        ISSN: 0022-5223            Impact factor:   5.209


  25 in total

1.  Spectrum of aortic operations in 300 patients with confirmed or suspected Marfan syndrome.

Authors:  Scott A LeMaire; Stacey A Carter; Irina V Volguina; Anne T Laux; Dianna M Milewicz; Garry W Borsato; Catherine K Cheung; John Bozinovski; Jennifer M Markesino; William K Vaughn; Joseph S Coselli
Journal:  Ann Thorac Surg       Date:  2006-06       Impact factor: 4.330

2.  Aortic enlargement and late reoperation after repair of acute type A aortic dissection.

Authors:  Andreas Zierer; Rochus K Voeller; Karen E Hill; Nicholas T Kouchoukos; Ralph J Damiano; Marc R Moon
Journal:  Ann Thorac Surg       Date:  2007-08       Impact factor: 4.330

Review 3.  Medical management of Marfan syndrome.

Authors:  Martin G Keane; Reed E Pyeritz
Journal:  Circulation       Date:  2008-05-27       Impact factor: 29.690

4.  Surgery for acute type A aortic dissection.

Authors:  T E David; S Armstrong; J Ivanov; S Barnard
Journal:  Ann Thorac Surg       Date:  1999-06       Impact factor: 4.330

5.  Rationale and design of the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC).

Authors:  Kim A Eagle
Journal:  Am Heart J       Date:  2008-12-17       Impact factor: 4.749

6.  The MOS 36-item Short-Form Health Survey (SF-36): III. Tests of data quality, scaling assumptions, and reliability across diverse patient groups.

Authors:  C A McHorney; J E Ware; J F Lu; C D Sherbourne
Journal:  Med Care       Date:  1994-01       Impact factor: 2.983

7.  Surgical treatment of patients enrolled in the national registry of genetically triggered thoracic aortic conditions.

Authors:  Howard K Song; Joseph E Bavaria; Mark W Kindem; Kathryn W Holmes; Dianna M Milewicz; Cheryl L Maslen; Reed E Pyeritz; Craig T Basson; Kim Eagle; H Eser Tolunay; Barbara L Kroner; Hal Dietz; Victor Menashe; Richard B Devereux; Patrice Desvigne-Nickens; William Ravekes; Jonathan W Weinsaft; Donald Brambilla; Mario P Stylianou; Tabitha Hendershot; Megan S Mitchell; Scott A LeMaire
Journal:  Ann Thorac Surg       Date:  2009-09       Impact factor: 4.330

8.  An aortic valve-sparing operation for patients with aortic incompetence and aneurysm of the ascending aorta.

Authors:  T E David; C M Feindel
Journal:  J Thorac Cardiovasc Surg       Date:  1992-04       Impact factor: 5.209

Review 9.  Marfan syndrome: from molecular pathogenesis to clinical treatment.

Authors:  Francesco Ramirez; Harry C Dietz
Journal:  Curr Opin Genet Dev       Date:  2007-04-27       Impact factor: 5.578

10.  Life expectancy in the Marfan syndrome.

Authors:  D I Silverman; K J Burton; J Gray; M S Bosner; N T Kouchoukos; M J Roman; M Boxer; R B Devereux; P Tsipouras
Journal:  Am J Cardiol       Date:  1995-01-15       Impact factor: 2.778

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  16 in total

1.  Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC) registry predicting predictors for aortic dissection: a new thought around the corner?

Authors:  Giacomo Murana; Antonio Pantaleo; Alessandro Parolari; Roberto Di Bartolomeo; Davide Pacini
Journal:  J Thorac Dis       Date:  2016-09       Impact factor: 2.895

Review 2.  A Review of Psychosocial Factors of Marfan Syndrome: Adolescents, Adults, Families, and Providers.

Authors:  Cory Nielsen; Ileana Ratiu; Mitra Esfandiarei; Angela Chen; Elif Seda Selamet Tierney
Journal:  J Pediatr Genet       Date:  2019-07-25

3.  Impact of ascending aortic prosthetic grafts on early postoperative descending aortic biomechanics on cardiac magnetic resonance imaging.

Authors:  Maria C Palumbo; Alberto Redaelli; Matthew Wingo; Katherine A Tak; Jeremy R Leonard; Jiwon Kim; Lisa Q Rong; Christine Park; Hannah W Mitlak; Richard B Devereux; Mary J Roman; Arindam RoyChoudury; Christopher Lau; Mario F L Gaudino; Leonard N Girardi; Jonathan W Weinsaft
Journal:  Eur J Cardiothorac Surg       Date:  2022-03-24       Impact factor: 4.191

4.  Health-Related Quality of Life in Thoracic Aortic Disease: Part II. After Surgery on the Proximal (Root, Ascending, Arch) Aorta.

Authors:  Christian Olsson; Anders Franco-Cereceda
Journal:  Aorta (Stamford)       Date:  2013-08-01

Review 5.  Potential predictors of severe cardiovascular involvement in Marfan syndrome: the emphasized role of genotype-phenotype correlations in improving risk stratification-a literature review.

Authors:  Zoltán Szabolcs; Kálmán Benke; Roland Stengl; Bence Ágg; Miklós Pólos; Gábor Mátyás; Gábor Szabó; Béla Merkely; Tamás Radovits
Journal:  Orphanet J Rare Dis       Date:  2021-05-31       Impact factor: 4.123

6.  Association between subjective well-being and perception of medical care system among patients with Marfan syndrome: A cross-sectional study.

Authors:  Tomoko Shimizu; Yasuko Shimizu
Journal:  Mol Genet Genomic Med       Date:  2021-05-05       Impact factor: 2.183

Review 7.  Marfan syndrome.

Authors:  Dianna M Milewicz; Alan C Braverman; Julie De Backer; Shaine A Morris; Catherine Boileau; Irene H Maumenee; Guillaume Jondeau; Arturo Evangelista; Reed E Pyeritz
Journal:  Nat Rev Dis Primers       Date:  2021-09-02       Impact factor: 65.038

8.  Preventing Acute Aortic Dissections: The Power of Familial Screening and Risk Assessment.

Authors:  Alana C Cecchi; Maura L Boerio; Isabella Marin; Amélie Pinard; Dianna M Milewicz
Journal:  J Am Heart Assoc       Date:  2022-04-06       Impact factor: 6.106

9.  Genetic variants in FBN-1 and risk for thoracic aortic aneurysm and dissection.

Authors:  Olga A Iakoubova; Carmen H Tong; Charles M Rowland; May M Luke; Veronica E Garcia; Joseph J Catanese; Remo M Moomiaie; Peter Sotonyi; Gyorgy Ascady; Demitrios Nikas; Panagiotis Dedelias; Maryann Tranquilli; John A Elefteriades
Journal:  PLoS One       Date:  2014-04-17       Impact factor: 3.240

10.  Possible extracardiac predictors of aortic dissection in Marfan syndrome.

Authors:  Bence Agg; Kálmán Benke; Bálint Szilveszter; Miklós Pólos; László Daróczi; Balázs Odler; Zsolt B Nagy; Ferenc Tarr; Béla Merkely; Zoltán Szabolcs
Journal:  BMC Cardiovasc Disord       Date:  2014-04-11       Impact factor: 2.298

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