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Outcomes in patients with cor triatriatum sinister

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1 Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA
2 Department of Cardiovascular Surgery Mayo Clinic, Rochester, Minnesota, USA

* Corresponding Author: Alexander Egbe, MBBS MPH, Department of Cardiovascular Medicine, Mayo Clinic, 200 First Street SW, Rochester MN 55905. Email: email

Congenital Heart Disease 2018, 13(4), 628-632. https://doi.org/10.1111/chd.12624

Abstract

Objective: To describe outcomes in patients with cor triatriatum sinister (CTS).
Design: Retrospective review of patients with CTS followed at Mayo Clinic Rochester from 1990 to 2016. Clinical notes, operative reports, and baseline imaging studies were reviewed including echocardiogram, magnetic resonance imaging, computed tomography, and cardiac catheterization.
Results: Fifty-seven patients (median age 34 years; men 32 (56%)) were enrolled. Definitive or suspected CTS diagnosis was made by transthoracic echocardiogram in 41 (72%) patients, and additional multimodality imaging was required in 39 (68%) patients. Of these 57 patients, initial diagnosis was made in adulthood in 35 (61%) patients, and 33 of 57 (58%) patients had additional congenital heart disease (CHD) diagnosis. A total of 27 (47%) patients required surgical resection of CTS membrane during median follow-up of 76 months, and these patients were younger at the time of CTS diagnosis (26 vs 41, P = 0.01) and more likely to have associated CHD (55% vs 45%, P = 0.02). There was one perioperative mortality and no late mortality. There was no recurrence of CTS membrane obstruction in the patients that underwent surgery. Similarly there was no significant increase in CTS membrane gradient in the patients that were managed conservatively.
Conclusions: The natural history of CTS is stability without progressive left atrial obstruction, especially in patients with isolated CTS and in those with initial CTS diagnosis made in adulthood. In patients requiring surgical membrane resection due to flow obstruction, surgery is safe and effective with very low risk of recurrence.

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APA Style
Fuchs, M.M., Connolly, H.M., Said, S.M., Egbe, A.C. (2018). Outcomes in patients with cor triatriatum sinister. Congenital Heart Disease, 13(4), 628-632. https://doi.org/10.1111/chd.12624
Vancouver Style
Fuchs MM, Connolly HM, Said SM, Egbe AC. Outcomes in patients with cor triatriatum sinister. Congeni Heart Dis. 2018;13(4):628-632 https://doi.org/10.1111/chd.12624
IEEE Style
M.M. Fuchs, H.M. Connolly, S.M. Said, and A.C. Egbe, “Outcomes in patients with cor triatriatum sinister,” Congeni. Heart Dis., vol. 13, no. 4, pp. 628-632, 2018. https://doi.org/10.1111/chd.12624



cc Copyright © 2018 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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