Impact of aortopulmonary collaterals on adverse events after total cavopulmonary connection

Author:

Osawa Takuya123ORCID,Schaeffer Thibault12,Borgmann Kristina4,Schmiel Mervin12,Staehler Helena12ORCID,Di Padua Chiara12,Heinisch Paul Philipp12ORCID,Piber Nicole5,Mutsuga Masato3ORCID,Hager Alfred4ORCID,Ewert Peter4ORCID,Hörer Jürgen12,Ono Masamichi12ORCID

Affiliation:

1. Department of Congenital and Pediatric Heart Surgery, German Heart Center Munich, Technische Universität München , Munich, Germany

2. Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität , Munich, Germany

3. Department of Cardiac Surgery, Nagoya University Graduate School of Medicine , Nagoya, Japan

4. Department of Congenital Heart Disease and Pediatric Cardiology, German Heart Center Munich, Technische Universität München , Munich, Germany

5. Department of Cardiovascular Surgery, German Heart Center Munich, Technische Universität München , Munich, Germany

Abstract

Abstract OBJECTIVES Effects of aortopulmonary collaterals (APCs) on outcomes after the total cavopulmonary connection (TCPC) are unclear. This study evaluated the incidence of APCs before and after TCPC and analysed the impacts of APCs on adverse outcomes. METHODS A total of 585 patients, who underwent TCPC from 1994 to 2020 and whose preoperative angiographies were available, were included. Pre-TCPC angiograms in all patients were used for the detection of APCs, and post-TCPC angiograms were evaluated in selected patients. Late adverse events included late death, protein-losing enteropathy (PLE) and plastic bronchitis (PB). RESULTS The median age at TCPC was 2.3 (1.8–3.4) years with a body weight of 12 (11–14) kg. APCs were found in 210 patients (36%) before TCPC and in 81 (14%) after TCPC. The closure of APCs was performed in 59 patients (10%) before TCPC, in 25 (4.2%) at TCPC and in 59 (10%) after TCPC. The occurrences of APCs before and after TCPC were not associated with short-term or mid-term mortality. The APCs before TCPC were associated with chylothorax (P = 0.025), prolonged chest tube duration (P = 0.021) and PB (P = 0.008). The APCs after TCPC were associated with PLE (P < 0.001) and PB (P < 0.001). With APCs following TCPC, freedom from PLE and PB was lower than without (P < 0.001, P < 0.001). CONCLUSIONS APCs before TCPC were associated with chylothorax, prolonged chest tube duration and PB. APCs after TCPC were associated with both PLE and PB. The presence of APCs might affect the lymph drainage system and increase the incidence of chylothorax, PLE and PB.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Pulmonary and Respiratory Medicine,General Medicine,Surgery

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