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Details

Autor(en) / Beteiligte
Titel
Impact of Left Atrial Appendage Amputation on Left Atrial Morphology and Rhythm after Off-Pump CABG
Ist Teil von
  • The Thoracic and cardiovascular surgeon, 2023-06, Vol.71 (4), p.273-281
Ort / Verlag
Germany
Erscheinungsjahr
2023
Quelle
MEDLINE
Beschreibungen/Notizen
  • Left atrial appendage (LAA) amputation concomitant to coronary artery bypass grafting (CABG) has become an increasingly performed technique in patients with atrial fibrillation (AF) or with sinus rhythm and a CHA2DS2-VASc score ≥2. However, LAA amputation has come under suspicion to cause postoperative atrial fibrillation (POAF) due to left atrial (LA) dilation. This study aims to assess this assumption in patients undergoing CABG in off-pump technique with and without amputation of the LAA. Patients who underwent isolated CABG in off-pump technique without history of AF were retrospectively examined. Cohorts were divided according to the concomitant execution of LAA amputation. LA volume was measured by transthoracic echocardiography and rhythm was analyzed by electrocardiography, medication protocol, and visit documentation. Propensity score (PS) matching was performed based on 20 preoperative risk variables to correct for selection bias. A total of 1,522 patients were enrolled, with 1,267 in the control group and 255 in the LAA amputation group. Occurrence of POAF was compared in 243 PS-matched patient pairs. Neither the unmatched cohort (odds ratio [OR] 0.82; 95% confidence interval or CI [0.61; 1.11],  = 0.19) nor the PS-matched cohort (OR 0.94; 95% CI [0.62; 1.41],  = 0.75) showed significant differences in POAF occurrence. Subgroup analysis of sex, use of β-blockers, pulmonary disease, ejection fraction, and CHA2DS2-VASc-Score also showed no tendencies. LA volume did not change significantly (  = 0.18, 95% CI [-0.29; 1.51]). Surgical amputation of the LAA concomitant to CABG did not lead to LA dilation and has no significant impact on the occurrence of POAF.
Sprache
Englisch
Identifikatoren
ISSN: 0171-6425
eISSN: 1439-1902
DOI: 10.1055/s-0041-1735809
Titel-ID: cdi_pubmed_primary_34808680

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