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Pericardial Effusions After the Arterial Switch Operation: A PHIS Database Review
Matthew F Mikulski1,2, Andrew Well1,2, Sujata Subramanian1,2
1Department of Surgery and Perioperative Care, 377659Dell Medical School, The University of Texas at Austin, Austin, TX, USA.
Insights
Pericardial effusion (PCE) occurred in 6.1% of arterial switch operations (ASO) and was linked to pleural effusions and mechanical support. While associated with increased morbidity and longer hospital stays, PCE did not impact mortality or readmission rates.
Area of Science:
- Pediatric Cardiac Surgery
- Cardiovascular Surgery
- Surgical Complications
Background:
- Pericardial effusion (PCE) is a known complication following pediatric cardiac surgery.
- The arterial switch operation (ASO) is a common procedure for dextro-transposition of the great arteries.
- Understanding PCE development and impact after ASO is crucial for patient outcomes.
Purpose of the Study:
- To investigate the incidence of pericardial effusion (PCE) after arterial switch operation (ASO).
- To identify risk factors associated with PCE development post-ASO.
- To evaluate the short-term and longitudinal impacts of PCE on pediatric patients undergoing ASO.
Main Methods:
- Retrospective review of the Pediatric Health Information System database.
- Inclusion of patients with dextro-transposition of the great arteries who underwent ASO between January 1, 2004, and March 31, 2022.
- Analysis using descriptive, univariate, and multivariable regression statistics to compare patients with and without PCE.
Main Results:
- Pericardial effusion (PCE) was diagnosed in 6.1% (300/4896) of patients post-ASO.
- PCE was significantly associated with acute renal failure, pleural effusions, and mechanical circulatory support.
- Patients with PCE experienced a longer postoperative length of stay but showed no difference in readmission rates or in-hospital mortality.
Conclusions:
- Pericardial effusion (PCE) is a notable complication after ASO, occurring in 6.1% of cases.
- Pleural effusions and mechanical circulatory support are identified as risk factors for PCE post-ASO.
- While PCE is linked to increased morbidity and prolonged hospitalization, it does not appear to affect in-hospital mortality or readmission rates.
Abstract:
Background: Pericardial effusion (PCE) is a significant complication after pediatric cardiac surgery. This study investigates PCE development after the arterial switch operation (ASO) and its short-term and longitudinal impacts. Methods: A retrospective review of the Pediatric Health Information System database. Patients with dextro-transposition of the great arteries who underwent ASO from January 1, 2004, to March 31, 2022, were identified. Patients with and without PCE were analyzed with descriptive, univariate, and multivariable regression statistics. Results: There were 4896 patients identified with 300 (6.1%) diagnosed with PCE. Thirty-five (11.7%) with PCE underwent pericardiocentesis. There were no differences in background demographics or concomitant procedures between those who developed PCE and those who did not. Patients who developed PCE more frequently had acute renal failure (N = 56 (18.7%) vs N = 603(13.1%), P = .006), pleural effusions (N = 46 (15.3%) vs N = 441 (9.6%), P = .001), mechanical circulatory support (N = 26 (8.7%) vs N = 199 (4.3%), P < .001), and had longer postoperative length of stay (15 [11-24.5] vs 13 [IQR: 9-20] days). After adjustment for additional factors, pleural effusions (OR = 1.7 [95% CI: 1.2-2.4]), and mechanical circulatory support (OR = 1.81 [95% CI: 1.15-2.85]) conferred higher odds of PCE. There were 2298 total readmissions, of which 46 (2%) had PCE, with no difference in median readmission rate for patients diagnosed with PCE at index hospitalization (median 0 [IQR: 0-1] vs 0 [IQR: 0-0], P = .208). Conclusions: PCE occurred after 6.1% of ASO and was associated with pleural effusions and mechanical circulatory support. PCE is associated with morbidity and prolonged length of stay; however, there was no association with in-hospital mortality or readmissions.
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