Catecholaminergic polymorphic ventricular tachycardia in pregnancy: a case report.
Cardiovascular disease in pregnancy
High-risk obstetrics
Inherited arrhythmia
Journal
Journal of medical case reports
ISSN: 1752-1947
Titre abrégé: J Med Case Rep
Pays: England
ID NLM: 101293382
Informations de publication
Date de publication:
09 Dec 2020
09 Dec 2020
Historique:
received:
01
05
2020
accepted:
28
10
2020
entrez:
9
12
2020
pubmed:
10
12
2020
medline:
15
5
2021
Statut:
epublish
Résumé
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a genetic disorder that can cause fatal tachyarrhythmias brought on by physical or emotional stress. There is little reported in the literature regarding management of CPVT in pregnancy much less during labor. A gravida 2, para 1 presented to our high-risk clinic at 15 weeks gestation with known CPVT. The Caucasian female patient had been diagnosed after experiencing a cardiac arrest following a motor vehicle accident and found to have a pathogenic cardiac ryanodine receptor mutation. An implantable cardioverter defibrillator was placed at that time. Her pregnancy was uncomplicated, and she was medically managed with metoprolol, flecainide, and verapamil. Her labor course and successful vaginal delivery were uncomplicated and involved a multidisciplinary team comprising specialists in electrophysiology, maternal fetal medicine, anesthesiology, general obstetrics, lactation, and neonatology. CPVT is likely underdiagnosed and, given that cardiovascular disease is a leading cause of death in pregnancy, it is important to bring further awareness to the diagnosis and management of this inherited arrhythmia syndrome in pregnancy.
Identifiants
pubmed: 33292493
doi: 10.1186/s13256-020-02569-5
pii: 10.1186/s13256-020-02569-5
pmc: PMC7724802
doi:
Substances chimiques
Ryanodine Receptor Calcium Release Channel
0
Flecainide
K94FTS1806
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
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