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Early outcomes of patients with Marfan syndrome and acute aortic type A dissection.
Farag, Mina; Büsch, Christopher; Rylski, Bartosz; Pöling, Jochen; Dohle, Daniel S; Sarvanakis, Konstantinos; Hagl, Christian; Krüger, Tobias; Detter, Christian; Holubec, Tomas; Borger, Michael A; Böning, Andreas; Karck, Matthias; Arif, Rawa.
Afiliação
  • Farag M; Department of Cardiac Surgery, Marfan Center, University Hospital Heidelberg, Heidelberg, Germany.
  • Büsch C; Institute of Medical Biometry and Informatics, University of Heidelberg, Heidelberg, Germany.
  • Rylski B; Faculty of Medicine, Department of Cardiovascular Surgery, Heart Center Freiburg University, University of Freiburg, Freiburg, Germany.
  • Pöling J; Department of Cardiac Surgery, Schuechtermann Clinic, Bad Rothenfelde, Germany.
  • Dohle DS; Department of Cardiothoracic and Vascular Surgery, University Hospital, Johannes Gutenberg University, Mainz, Germany.
  • Sarvanakis K; Clinic of Cardiothoracic Surgery, University Hospital Augsburg, Augsburg, Germany.
  • Hagl C; Department of Cardiac Surgery, University Hospital, LMU Munich, Munich, Germany.
  • Krüger T; Department of Thoracic and Cardiovascular Surgery, University Medical Center Tübingen, Tübingen, Germany.
  • Detter C; Department of Cardiovascular Surgery, University Heart Center Hamburg, Hamburg, Germany.
  • Holubec T; Department of Cardiovascular Surgery, University Hospital and Johann Wolfgang Goethe University Frankfurt, Frankfurt/Main, Germany.
  • Borger MA; University Clinic of Cardiac Surgery, Leipzig Heart Center, Leipzig, Germany.
  • Böning A; Department of Cardiovascular Surgery, University Hospital Giessen, Giessen, Germany.
  • Karck M; Department of Cardiac Surgery, Marfan Center, University Hospital Heidelberg, Heidelberg, Germany.
  • Arif R; Department of Cardiac Surgery, Marfan Center, University Hospital Heidelberg, Heidelberg, Germany. Electronic address: rawa.arif@med.uni-heidelberg.de.
J Thorac Cardiovasc Surg ; 166(1): 25-34.e8, 2023 07.
Article em En | MEDLINE | ID: mdl-34446289
ABSTRACT

BACKGROUND:

Acute aortic Stanford type A dissection remains a frequent and life-limiting event for patients with Marfan syndrome. Outcome results in this high-risk group are limited.

METHODS:

The German Registry for Acute Aortic Dissection Type A collected the data of 56 centers between July 2006 and June 2015. Of 3385 patients undergoing operations for acute aortic Stanford type A dissection, 117 (3.5%) were diagnosed with Marfan syndrome. We performed a propensity score match comparing patients with Marfan syndrome with patients without Marfan syndrome in a 12 fashion.

RESULTS:

Patients with Marfan syndrome were significantly younger (42.9 vs 62.2 years; P < .001), predominantly male (76.9% vs 62.9%; P = .002), and less catecholamine dependent (9.4% vs 20.3%; P = .002) compared with the unmatched cohort. They presented with aortic regurgitation (41.6% vs 23.0%; P < .001) and involvement of the supra-aortic vessels (50.4% vs 39.5%; P = .017) more often. Propensity matching revealed 82 patients with Marfan syndrome (21 female) with no significant differences in baseline characteristics compared with patients without Marfan syndrome (n = 159, 36 female; P = .607). Although root preservation was more frequent in patients with Marfan syndrome, procedure types did not differ significantly (18.3% vs 10.7%; P = .256). Aortic arch surgery was performed more frequently in matched patients (87.5% vs 97.8%; P = .014). Thirty-day mortality did not differ between patients with and without Marfan syndrome (19.5% vs 20.1%; P = .910). Multivariate regression showed no influence of Marfan syndrome on 30-day mortality (odds ratio, 0.928; 95% confidence interval, 0.346-2.332; P = .876).

CONCLUSIONS:

Marfan syndrome does not adversely affect 30-day outcomes after surgical repair for acute aortic Stanford type A dissection compared with a matched cohort. Long-term outcome analysis is needed to account for the influence of further downstream interventions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dissecção Aórtica / Síndrome de Marfan Limite: Female / Humans / Male Idioma: En Revista: J Thorac Cardiovasc Surg Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dissecção Aórtica / Síndrome de Marfan Limite: Female / Humans / Male Idioma: En Revista: J Thorac Cardiovasc Surg Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha