Identification of new-onset atrial fibrillation after cardiac surgery in Vietnam. A feasibility study of a novel screening strategy in a limited-resource setting: study protocol.

Autor:	Ngo THL; Cardiovascular Centre, E Hospital, Hanoi, Vietnam., Vu VB; Cardiovascular Centre, E Hospital, Hanoi, Vietnam., Nguyen CH; Cardiovascular Centre, E Hospital, Hanoi, Vietnam., Le TD; Cardiovascular Centre, E Hospital, Hanoi, Vietnam., Hoang TK; Cardiovascular Centre, E Hospital, Hanoi, Vietnam., Freedman B; Heart Research Institute, and Charles Perkins Centre, University of Sydney, Sydney, Australia., Lowres N; Heart Research Institute, and Charles Perkins Centre, University of Sydney, Sydney, Australia.
Jazyk:	angličtina
Zdroj:	BMJ open [BMJ Open] 2018 Sep 04; Vol. 8 (9), pp. e020800. Date of Electronic Publication: 2018 Sep 04.
DOI:	10.1136/bmjopen-2017-020800
Abstrakt:	Introduction: Atrial fibrillation (AF) developing after cardiac surgery is the most common postoperative complication with an incidence up to 50%. The presence of postoperative AF is associated with significant morbidity, mortality and economic burden. However, in Vietnam, data on AF postcardiac surgery are limited, in part due to a shortage of screening equipment. This project aims to identify the incidence, risk factors and postoperative complications of new-onset postoperative AF after cardiac surgery, and the feasibility of introducing a novel screening strategy using the combination of two portable devices to detect AF. Methods and Analysis: This is a feasibility study examining patients who are (1) ≥18 years old; (2) undergoing coronary artery bypass graft and/or valve surgery and (3) in normal sinus rhythm prior to their operation. Patients with congenital heart disease, a prior history of AF or those who require a pacemaker after surgery will be excluded. All patients will be followed up for the duration of their hospitalisation. The screening strategy will include monitoring the continuous ECG tracing in the intensive care unit, and if AF is suspected, a 30 s lead-1 ECG will be recorded using the smartphone-based AliveCor Kardia Mobile. On the postoperative wards, blood pressure will be measured three times daily using a modified blood pressure device (Microlife BP200 Afib): and if AF is suspected a 30 s ECG will be recorded using the AliveCor Kardia Mobile. A 12-lead ECG may be ordered subsequently if clinically indicated. The primary outcome is the incidence of postoperative AF. Secondary outcomes include establishing the risk factors and complications associated with postoperative AF; and the barriers and facilitators of the screening strategy. Ethics and Dissemination: Ethics approval was granted by Scientific Board of Cardiovascular Centre, E Hospital on 28 September, 2017. Study results will be disseminated through local and international conferences and peer-reviewed publications. Competing Interests: Competing interests: None declared. (© Author(s) (or their employer(s)) 2018. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)
Databáze:	MEDLINE
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