Hypoplasia, pseudocoarctation and coarctation of the aorta - a systematic review.

Autor: Singh S; Division of Hospital Internal Medicine, Mayo Clinic, Scottsdale, USA., Hakim FA; Division of Cardiovascular Diseasey, Mayo Clinic, Scottsdale, USA., Sharma A; Division of Cardiovascular Diseasey, Mayo Clinic, Scottsdale, USA., Roy RR; Division of Cardiovascular Diseasey, Mayo Clinic, Scottsdale, USA., Panse PM; Division of Cardiovascular Diseases, Sanger Heart & Vascular Institute-Charlotte-Blythe, Charlotte, USA., Chandrasekaran K; Division of Cardiovascular Diseasey, Mayo Clinic, Scottsdale, USA., Alegria JR; Division of Diagnostic Radiology, Mayo Clinic, Scottsdale, USA., Mookadam F; Division of Cardiovascular Diseasey, Mayo Clinic, Scottsdale, USA. Electronic address: mookadam.farouk@mayo.edu.
Jazyk: angličtina
Zdroj: Heart, lung & circulation [Heart Lung Circ] 2015 Feb; Vol. 24 (2), pp. 110-8. Date of Electronic Publication: 2014 Aug 23.
DOI: 10.1016/j.hlc.2014.08.006
Abstrakt: Aortic arch abnormalities are uncommon and may be seen in association with other congenital cardiac anomalies. Coarctation, pseudocoarctation and hypoplastic aortic arch are known aortic arch abnormalities, with the former being well studied, whilst for the latter two, much less is known. There are similarities and differences that are important to distinguish among these three conditions in order to avoid errors in diagnosis that may result in unnecessary investigations, which may in turn result in physical or emotional harm to the patient. For this reason, we present a systematic review of the published literature providing an evidence-based overview that may be helpful to clinicians when faced with this diagnostic dilemma.
(Copyright © 2014 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ). Published by Elsevier B.V. All rights reserved.)
Databáze: MEDLINE