Acute myocardial infarction in a patient with congenitally corrected transposition of the great arteries and complex coronary anatomy-a case report.

Acute myocardial infarction Case report Congenitally corrected transposition of the great arteries Coronary artery anomalies

Journal

European heart journal. Case reports
ISSN: 2514-2119
Titre abrégé: Eur Heart J Case Rep
Pays: England
ID NLM: 101730741

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 14 02 2022
revised: 21 03 2022
accepted: 30 10 2022
entrez: 21 11 2022
pubmed: 22 11 2022
medline: 22 11 2022
Statut: epublish

Résumé

Congenitally corrected transposition of the great arteries (ccTGA) is a rare congenital heart anomaly with atrioventricular and ventriculoarterial discordance that is often associated with other cardiac and coronary artery anomalies. Here, we report a case of a patient with ccTGA and non-ST elevation myocardial infarction (NSTEMI) with challenging coronary anatomy that was treated with stress-perfusion cardiac magnetic resonance imaging (spCMR) guided percutaneous coronary intervention (PCI). A 46-year-old male smoker with ccTGA, dyslipidaemia, diabetes Type 2 managed with dietary restrictions and a family history of premature myocardial infarction, presented with typical chest pain, elevated cardiac troponin levels and ECG-changes indicative of ischaemia. The patient was diagnosed with NSTEMI and underwent initial urgent coronary angiography (CA) without apparent significant stenosis, although the right coronary artery (RCA) could not be selectively investigated. The patient had coronary anatomy 1R-2LCX according to the Leiden convention, which is the usual anatomy in patients with ccTGA. Despite this, CA was challenging due to the different anatomy compared with individuals with normally positioned great vessels. The patient remained highly symptomatic with chest pain at moderate exertion. To improve identification of the anatomic location and extent of ischaemia, we performed spCMR with adenosine. This revealed a limited septal infarction (likely embolic) in the right ventricle and reversible ischaemia in two inferior right ventricular segments. A second angiography, selectively investigating RCA demonstrated a significant stenosis in the distal RCA that was successfully treated with a drug-eluting stent. Fractional flow reserve (FFR) measurements of the left coronary arteries demonstrated hemodynamically non-significant stenosis. The patient's symptoms resolved, and he remained asymptomatic at one month follow-up. This ccTGA patient had multiple risk factors for coronary artery disease and presented with NSTEMI. Diagnosis and treatment were challenging due to complex cardiac anatomy and associated different origins of the coronary arteries. We highlight the importance of careful evaluation of the coronary anatomy and functional testing using for example spCMR and FFR to target the culprit coronary vessel(s) in ccTGA complicated by NSTEMI.

Sections du résumé

Background UNASSIGNED
Congenitally corrected transposition of the great arteries (ccTGA) is a rare congenital heart anomaly with atrioventricular and ventriculoarterial discordance that is often associated with other cardiac and coronary artery anomalies. Here, we report a case of a patient with ccTGA and non-ST elevation myocardial infarction (NSTEMI) with challenging coronary anatomy that was treated with stress-perfusion cardiac magnetic resonance imaging (spCMR) guided percutaneous coronary intervention (PCI).
Case summary UNASSIGNED
A 46-year-old male smoker with ccTGA, dyslipidaemia, diabetes Type 2 managed with dietary restrictions and a family history of premature myocardial infarction, presented with typical chest pain, elevated cardiac troponin levels and ECG-changes indicative of ischaemia. The patient was diagnosed with NSTEMI and underwent initial urgent coronary angiography (CA) without apparent significant stenosis, although the right coronary artery (RCA) could not be selectively investigated. The patient had coronary anatomy 1R-2LCX according to the Leiden convention, which is the usual anatomy in patients with ccTGA. Despite this, CA was challenging due to the different anatomy compared with individuals with normally positioned great vessels. The patient remained highly symptomatic with chest pain at moderate exertion. To improve identification of the anatomic location and extent of ischaemia, we performed spCMR with adenosine. This revealed a limited septal infarction (likely embolic) in the right ventricle and reversible ischaemia in two inferior right ventricular segments. A second angiography, selectively investigating RCA demonstrated a significant stenosis in the distal RCA that was successfully treated with a drug-eluting stent. Fractional flow reserve (FFR) measurements of the left coronary arteries demonstrated hemodynamically non-significant stenosis. The patient's symptoms resolved, and he remained asymptomatic at one month follow-up.
Discussion UNASSIGNED
This ccTGA patient had multiple risk factors for coronary artery disease and presented with NSTEMI. Diagnosis and treatment were challenging due to complex cardiac anatomy and associated different origins of the coronary arteries. We highlight the importance of careful evaluation of the coronary anatomy and functional testing using for example spCMR and FFR to target the culprit coronary vessel(s) in ccTGA complicated by NSTEMI.

Identifiants

pubmed: 36405539
doi: 10.1093/ehjcr/ytac423
pii: ytac423
pmc: PMC9668067
doi:

Types de publication

Case Reports

Langues

eng

Pagination

ytac423

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology.

Déclaration de conflit d'intérêts

Conflict of interest: Fahd Asaad: None to declare. Peder Sörensson: Honoraria and consultant fees (Pfizer). Andreas Rück: Research grants to our institution (Boston Scientific). Consulting fees (Boston Scientific). Consulting, proctoring fees (Boston Scientific). Advisory Board (Boston Scientific). Edit Nagy: None to declare. Juliane Jurga: None to declare. Marcus Ståhlberg: None to declare..

Références

Case Rep Med. 2017;2017:7565870
pubmed: 28280512
J Thorac Cardiovasc Surg. 1996 May;111(5):988-97
pubmed: 8622324
Can J Cardiol. 2010 Mar;26(3):e98-117
pubmed: 20352139
Eur Heart J. 2020 Nov 14;41(43):4153-4154
pubmed: 33128054
Int J Cardiol. 2002 Dec;86(2-3):207-16
pubmed: 12419558
Eur Heart J Cardiovasc Imaging. 2022 Feb 22;23(3):412-422
pubmed: 33585887
Eplasty. 2013;13:e6
pubmed: 23409204
Circ Cardiovasc Imaging. 2014 Sep;7(5):849-51
pubmed: 25227238

Auteurs

Fahd Asaad (F)

Medical unit Cardiology, Heart, Vascular and Neuro Theme, Karolinska University Hospital, Eugeniavägen 23, 171 76 Stockholm and Department of Medicine Solna, Solnavägen 1, 171 77 Solna, Karolinska Institute, Stockholm, Sweden.

Peder Sörensson (P)

Medical unit Cardiology, Heart, Vascular and Neuro Theme, Karolinska University Hospital, Eugeniavägen 23, 171 76 Stockholm and Department of Medicine Solna, Solnavägen 1, 171 77 Solna, Karolinska Institute, Stockholm, Sweden.

Andreas Rück (A)

Medical unit Cardiology, Heart, Vascular and Neuro Theme, Karolinska University Hospital, Eugeniavägen 23, 171 76 Stockholm and Department of Medicine Solna, Solnavägen 1, 171 77 Solna, Karolinska Institute, Stockholm, Sweden.

Edit Nagy (E)

Medical unit Cardiology, Heart, Vascular and Neuro Theme, Karolinska University Hospital, Eugeniavägen 23, 171 76 Stockholm and Department of Medicine Solna, Solnavägen 1, 171 77 Solna, Karolinska Institute, Stockholm, Sweden.

Juliane Jurga (J)

Medical unit Cardiology, Heart, Vascular and Neuro Theme, Karolinska University Hospital, Eugeniavägen 23, 171 76 Stockholm and Department of Medicine Solna, Solnavägen 1, 171 77 Solna, Karolinska Institute, Stockholm, Sweden.

Marcus Ståhlberg (M)

Medical unit Cardiology, Heart, Vascular and Neuro Theme, Karolinska University Hospital, Eugeniavägen 23, 171 76 Stockholm and Department of Medicine Solna, Solnavägen 1, 171 77 Solna, Karolinska Institute, Stockholm, Sweden.

Classifications MeSH