Isolation of the right subclavian artery. Mini-invasive repair

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064203%3A_____%2F20%3A10410827" target="_blank" >RIV/00064203:_____/20:10410827 - isvavai.cz</a>

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=d_Z-7jpa~i" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=d_Z-7jpa~i</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.rec.2018.11.007" target="_blank" >10.1016/j.rec.2018.11.007</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Isolation of the right subclavian artery. Mini-invasive repair

Popis výsledku v původním jazyce

Isolation of the right subclavian artery (RSA) is a rare aortic arch anomaly, defined as a loss of continuity between the subclavian artery and the aorta with persistent connection to the homolateral pulmonary artery (PA) through a patent or nonpatent arterial duct. Its presence as an isolated anomaly is extremely rare. It is usually combined with complex cardiac malformations. We report right subclavian artery isolation in a child with normal left-sided aortic arch presenting as a single anomaly. A 4-year-old girl was referred with a diagnosis of patent ductus arteriosus (PDA). On physical examination, a continuous murmur was observed. Arterial pulses on the right upper arm were weak compared with the left arm. Echocardiography revealed an RSA arising from the right pulmonary artery (RPA) via a 9-mm wide PDA with a left-to-right shunt to the RPA. During cardiac catheterization, the mean PA pressure was slightly increased to 20 mmHg and a left-to-right shunt of 47% was calculated (Figure 1). Computed tomography angiography was performed for 3-dimensional imaging (Figure 2, left pulmonary artery [LPA]). The patient underwent a division and reimplantation of the RSA to the ascending aorta via an upper partial sternotomy and limited skin incision. The procedure is shown in Video 1 of the supplementary data. The surgical reimplantation approach can avoid subclavian steal in the future and the possibility of neurological syncope and suboptimal upper limb growth. Although some cases of subclavian artery isolation might be associated with Di George syndrome, our patient did not have the typical phenotype and normal thymus was seen during the operation. Consequently, genetic testing was not performed.

Název v anglickém jazyce

Isolation of the right subclavian artery. Mini-invasive repair

Popis výsledku anglicky

Isolation of the right subclavian artery (RSA) is a rare aortic arch anomaly, defined as a loss of continuity between the subclavian artery and the aorta with persistent connection to the homolateral pulmonary artery (PA) through a patent or nonpatent arterial duct. Its presence as an isolated anomaly is extremely rare. It is usually combined with complex cardiac malformations. We report right subclavian artery isolation in a child with normal left-sided aortic arch presenting as a single anomaly. A 4-year-old girl was referred with a diagnosis of patent ductus arteriosus (PDA). On physical examination, a continuous murmur was observed. Arterial pulses on the right upper arm were weak compared with the left arm. Echocardiography revealed an RSA arising from the right pulmonary artery (RPA) via a 9-mm wide PDA with a left-to-right shunt to the RPA. During cardiac catheterization, the mean PA pressure was slightly increased to 20 mmHg and a left-to-right shunt of 47% was calculated (Figure 1). Computed tomography angiography was performed for 3-dimensional imaging (Figure 2, left pulmonary artery [LPA]). The patient underwent a division and reimplantation of the RSA to the ascending aorta via an upper partial sternotomy and limited skin incision. The procedure is shown in Video 1 of the supplementary data. The surgical reimplantation approach can avoid subclavian steal in the future and the possibility of neurological syncope and suboptimal upper limb growth. Although some cases of subclavian artery isolation might be associated with Di George syndrome, our patient did not have the typical phenotype and normal thymus was seen during the operation. Consequently, genetic testing was not performed.

Druh

J_SC - Článek v periodiku v databázi SCOPUS

CEP obor

—

OECD FORD obor

30201 - Cardiac and Cardiovascular systems

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2020

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Revista Española de Cardiología

ISSN

0300-8932

e-ISSN

1579-2242

Svazek periodika

73

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

ES - Španělské království

Počet stran výsledku

1

Strana od-do

169-169

Kód UT WoS článku

000514849200012

EID výsledku v databázi Scopus

2-s2.0-85073708396