Coronary artery changes 3 years after reimplantation of an anomalous right coronary artery

Woezik, H. Van Meurs-Van; Serruys, P.W.; Reiber, J.H.C.; E, Bos; Villeneuve, V. H. de

doi:10.1093/oxfordjournals.eurheartj.a061628

Cited by 9 publications

(4 citation statements)

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“…The evolution of aneurysmal coronary after surgical correction is still under investigation. Van-Meurs-van-Woezik et al show reduction in the size of coronary artery 3 years after reimplantation of ARCAPA [7]. We suggest aspirin therapy and long-term follow-up with echocardiographic evaluation until the coronary artery returns to the normal size.…”

Section: Discussionmentioning

confidence: 73%

Anomalous origin of right coronary artery from pulmonary artery with aneurysmal coronary arteries

et al. 2016

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Popisujeme případ 16letého asymptomatického chlapce, odeslaného na naše pracoviště pro vyšetření srdečního šelestu. Echokardiografi cké i angiografi cké vyšetření prokázalo anomálii v odstupu pravé koronární tepny z plicnice spolu s dilatací levé koronární tepny a několika velkými kolaterálami. Cílem chirurgického řešení je vytvoření fyziologického koronárního oběhu.

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Section: Discussionmentioning

confidence: 73%

Anomalous origin of right coronary artery from pulmonary artery with aneurysmal coronary arteries

et al. 2016

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“…So far, only case reports or small series have been reported for children operated for ARCAPA. 8,9,[12][13][14][15][16][17] Table 2 provides a summary of the prior reports in the literature on children with ARCAPA reimplantation and follow-up. To our knowledge, this report presents the largest cohort of children treated for ARCAPA with and without co-existing CHD and for the longest follow-up time.…”

Section: Discussionmentioning

confidence: 99%

Long-term outcomes after repair for anomalous right coronary artery from the pulmonary artery

et al. 2022

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Anomalous right coronary artery from pulmonary artery (ARCAPA) is a rare congenital heart disease that can lead to abnormal coronary perfusion and a need for surgical repair. Here, we report the outcomes of patients who underwent ARCAPA surgery within the Pediatric Cardiac Care Consortium (PCCC), a North American registry of interventions for paediatric heart diseases. We queried the PCCC for patients undergoing surgical repair for ARCAPA at <18 years of age between 1982 and 2003. Outcomes were obtained from the PCCC and after linkage with the National Death Index (NDI) and the Organ Procurement and Transplantation Network (OPTN) through 2019. Twenty-four patients (males: 15) were identified having surgery for ARCAPA at a median age of 5.8 (IQR 2.7–10.3) years. Of them, 23 cases were considered “simple” (without major intracardiac disease) and one “complex” (co-existing with tetralogy of Fallot). Five patients presented with symptoms [chest pain (1), dyspnoea on exertion (2) or history of syncope (2)]; while the remaining 19 patients were referred for evaluation of either murmur or co-existing CHD. There was no in-hospital mortality after the surgical repair. Fourteen patients had sufficient identifiers for NDI/OPTN linkage; among them, only one death occurred from unrelated non-cardiac causes within a median period of 19.4 years of follow-up (IQR: 18–24.6). Outcomes were excellent after reimplantation up to 25 years later and further longitudinal monitoring is important to understand the interaction of pre-existing coronary pathology with the effects of ageing.

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“…Angiokardiographisch lä ßt sich die Diagnose durch die Darstellung der Koronarien sichern; der von uns gefundene Sä ttigungssprung zwischen Pulmonalarterie und rechtem Ventrikel ist nicht regelhaft nachweisbar und seine Abwesenheit spricht in keinem Fall gegen den Fehlabgang der rechten Koronararterie [22,24,25].…”

Section: Introductionunclassified

“…Bland-White-Garland-Syndrom die rechte Koronararterie am Abgang aus der Pulmonalarterie ligiert [20,22] und hierdurch nicht immer ü berzeugende Resultate erzielen kö nnen, wird heute -nicht zuletzt durch die positiven Erfahrungen bei der Switch-Operation zur Korrektur der Transposition der großen Gefäße -mö glichst eine Reimplantation der rechten Koronararterie in die Aorta mit Perikardplastik der Pulmonalarterie durchgefü hrt [14,24,25].…”

Section: Introductionunclassified

Fehlerhafter Abgang der rechten Koronararterie aus der A. pulmonalis bei einem asymptomatischen Schulkind

Schnellbacher¹,

Koch

Schmitz

et al. 1997

Monatsschrift Kinderheilkunde

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Coronary artery changes 3 years after reimplantation of an anomalous right coronary artery

Cited by 9 publications

References 0 publications

Anomalous origin of right coronary artery from pulmonary artery with aneurysmal coronary arteries

Anomalous origin of right coronary artery from pulmonary artery with aneurysmal coronary arteries

Long-term outcomes after repair for anomalous right coronary artery from the pulmonary artery

Fehlerhafter Abgang der rechten Koronararterie aus der A. pulmonalis bei einem asymptomatischen Schulkind

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