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Clinical and procedural implications of congenital vena cava anomalies in adults: A systematic review.
Shafi, Irfan; Hassan, Abubakar A I; Akers, Katherine G; Bashir, Riyaz; Alkhouli, Mohamad; Weinberger, Jarret J; Abidov, Aiden.
Afiliação
  • Shafi I; Department of Internal Medicine, Wayne State University/Detroit Medical Center, Detroit, MI, USA. Electronic address: ishafi@med.wayne.edu.
  • Hassan AAI; Department of Internal Medicine, Wayne State University/Detroit Medical Center, Detroit, MI, USA.
  • Akers KG; Shiffman Medical Library, Wayne State University, Detroit, MI, USA.
  • Bashir R; Department of Cardiovascular Diseases, Temple University Hospital, PA, USA.
  • Alkhouli M; Department of Cardiology, Mayo Clinic School of Medicine, Rochester, MN, USA.
  • Weinberger JJ; Department of Internal Medicine, Wayne State University/Detroit Medical Center, Detroit, MI, USA.
  • Abidov A; Cardiology Section, John D. Dingell VA Medical Center, Detroit, MI, USA; Division of Cardiology, Wayne State University, Detroit, MI, USA.
Int J Cardiol ; 315: 29-35, 2020 09 15.
Article em En | MEDLINE | ID: mdl-32434672
ABSTRACT

BACKGROUND:

Although congenital vena cava (CVC) anomalies in adults have implications for surgical and radiological interventions, the literature is scare and disparate. The aim of this systematic review was to assess cardiovascular clinical and procedural implications of CVC anomalies in adults without congenital heart disease. METHODS AND

RESULTS:

We searched PubMed and EMBASE from database conception through October 2018 for English-language studies describing the epidemiology of CVC anomalies or their clinical or procedural implications in humans. Two independent reviewers screened 7093 records and identified 16 relevant studies. We found two major implications of CVC anomalies 1) congenital inferior vena cava (CIVC) anomalies are associated with a 50-100-fold higher risk of deep venous thrombosis, particularly among younger patients, and 2) persistent left superior vena cava (PLSVC) is associated with a 2-3-fold higher risk of supraventricular arrhythmias. PLSVC also poses technical challenges to cardiovascular electronic device implantation, requiring alterations in surgical approach and lengthening procedure and X-ray exposure times. Due to the large disparity in reported prevalence rates of CIVC anomalies, we performed a meta-analysis of CIVC anomaly prevalence including 8 studies, which showed a weighted prevalence of 6.8% (95% CI, 4.5-9.2%).

CONCLUSION:

These findings challenge the notion that CVC anomalies are rare and asymptomatic in adults. Rather, the literature indicates that CVC anomalies are not uncommon and have important clinical and procedural implications. To further understand the prevalence and implications of CVC anomalies, a robust US population-based study and nationwide registry is warranted in the current era of venous interventions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Malformações Vasculares / Cardiopatias Congênitas Tipo de estudo: Systematic_reviews Limite: Adult / Humans Idioma: En Revista: Int J Cardiol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Malformações Vasculares / Cardiopatias Congênitas Tipo de estudo: Systematic_reviews Limite: Adult / Humans Idioma: En Revista: Int J Cardiol Ano de publicação: 2020 Tipo de documento: Article