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dc.contributor.authorQuah, JX
dc.contributor.authorHofmeyr, L
dc.contributor.authorHaqqani, H
dc.contributor.authorClarke, A
dc.contributor.authorRahman, A
dc.contributor.authorPohlner, P
dc.contributor.authorRadford, D
dc.contributor.authorNicolae, M
dc.date.accessioned2020-11-13T05:45:17Z
dc.date.available2020-11-13T05:45:17Z
dc.date.issued2014
dc.identifier.issn1747-079X
dc.identifier.doi10.1111/chd.12125
dc.identifier.urihttp://hdl.handle.net/10072/399278
dc.description.abstractALCAPA (anomalous left coronary artery from pulmonary artery) syndrome is a rare congenital abnormality that involves an anomalous insertion of the left coronary artery into the pulmonary artery. Ninety percent of patients present in the first year of life with signs and symptoms of heart failure or sudden cardiac death secondary to chronic myocardial ischemia. There have been an increasing number of reports of ALCAPA patients surviving to adulthood. There seems, however, to be a tendency to die suddenly in the third decade of life. Adult survivors are either asymptomatic or present with mitral regurgitation, cardiomyopathy, myocardial ischemia, or malignant arrhythmias. The management of the older patient presenting with symptoms resulting from ischemia and progressive left ventricular dysfunction remains a challenge. Treatment is largely based on guidelines for adult congenital heart disease management and an extrapolation of evidence from heart failure practice. Currently, surgical reimplantation of the anomalous coronary onto the aorta is the mainstay of treatment. The management of heart failure, sudden cardiac death, and ventricular arrhythmia present problems that are not addressed by reimplantation of the anomalous vessel alone. In this report, we present two cases with different modes of presentation and discuss treatment options.
dc.description.peerreviewedYes
dc.languageEnglish
dc.language.isoeng
dc.publisherComputers, Materials and Continua (Tech Science Press)
dc.relation.ispartofpagefromE185
dc.relation.ispartofpagetoE194
dc.relation.ispartofissue6
dc.relation.ispartofjournalCongenital Heart Disease
dc.relation.ispartofvolume9
dc.subject.fieldofresearchCardiovascular medicine and haematology
dc.subject.fieldofresearchcode3201
dc.subject.keywordsALCAPA
dc.subject.keywordsCardiomyopathy
dc.subject.keywordsCoronary Artery Anomaly
dc.subject.keywordsImplantable Cardioverter Defibrillator
dc.subject.keywordsMyocardial Ischemia
dc.titleThe management of the older adult patient with anomalous left coronary artery from the pulmonary artery syndrome: A presentation of two cases and review of the literature
dc.typeJournal article
dc.type.descriptionC1 - Articles
dcterms.bibliographicCitationQuah, JX; Hofmeyr, L; Haqqani, H; Clarke, A; Rahman, A; Pohlner, P; Radford, D; Nicolae, M, The management of the older adult patient with anomalous left coronary artery from the pulmonary artery syndrome: A presentation of two cases and review of the literature, Congenital Heart Disease, 2014, 9 (6), pp. E185-E194
dcterms.dateAccepted2013-07-03
dc.date.updated2020-11-13T04:43:25Z
gro.hasfulltextNo Full Text
gro.griffith.authorRahman, Atifur


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