Impact of Major Residual Lesions on Outcomes After Surgery for Congenital Heart Disease.


Journal

Journal of the American College of Cardiology
ISSN: 1558-3597
Titre abrégé: J Am Coll Cardiol
Pays: United States
ID NLM: 8301365

Informations de publication

Date de publication:
18 05 2021
Historique:
received: 27 12 2020
revised: 04 03 2021
accepted: 22 03 2021
entrez: 14 5 2021
pubmed: 15 5 2021
medline: 16 11 2021
Statut: ppublish

Résumé

Many factors affect outcomes after congenital cardiac surgery. The RLS (Residual Lesion Score) study explored the impact of severity of residual lesions on post-operative outcomes across operations of varying complexity. In a prospective, multicenter, observational study, 17 sites enrolled 1,149 infants undergoing 5 common operations: tetralogy of Fallot repair (n = 250), complete atrioventricular septal defect repair (n = 249), arterial switch operation (n = 251), coarctation or interrupted arch with ventricular septal defect (VSD) repair (n = 150), and Norwood operation (n = 249). The RLS was assigned based on post-operative echocardiography and clinical events: RLS 1 (trivial or no residual lesions), RLS 2 (minor residual lesions), or RLS 3 (reintervention for or major residual lesions before discharge). The primary outcome was days alive and out of hospital within 30 post-operative days (60 for Norwood). Secondary outcomes assessed post-operative course, including major medical events and days in hospital. RLS 3 (vs. RLS 1) was an independent risk factor for fewer days alive and out of hospital (p ≤ 0.008) and longer post-operative hospital stay (p ≤ 0.02) for all 5 operations, and for all secondary outcomes after coarctation or interrupted arch with VSD repair and Norwood (p ≤ 0.03). Outcomes for RLS 1 versus 2 did not differ consistently. RLS alone explained 5% (tetralogy of Fallot repair) to 20% (Norwood) of variation in the primary outcome. Adjusting for pre-operative factors, residual lesions after congenital cardiac surgery impacted in-hospital outcomes across operative complexity with greatest impact following complex operations. Minor residual lesions had minimal impact. These findings may provide guidance for surgeons when considering short-term risks and benefits of returning to bypass to repair residual lesions.

Sections du résumé

BACKGROUND
Many factors affect outcomes after congenital cardiac surgery.
OBJECTIVES
The RLS (Residual Lesion Score) study explored the impact of severity of residual lesions on post-operative outcomes across operations of varying complexity.
METHODS
In a prospective, multicenter, observational study, 17 sites enrolled 1,149 infants undergoing 5 common operations: tetralogy of Fallot repair (n = 250), complete atrioventricular septal defect repair (n = 249), arterial switch operation (n = 251), coarctation or interrupted arch with ventricular septal defect (VSD) repair (n = 150), and Norwood operation (n = 249). The RLS was assigned based on post-operative echocardiography and clinical events: RLS 1 (trivial or no residual lesions), RLS 2 (minor residual lesions), or RLS 3 (reintervention for or major residual lesions before discharge). The primary outcome was days alive and out of hospital within 30 post-operative days (60 for Norwood). Secondary outcomes assessed post-operative course, including major medical events and days in hospital.
RESULTS
RLS 3 (vs. RLS 1) was an independent risk factor for fewer days alive and out of hospital (p ≤ 0.008) and longer post-operative hospital stay (p ≤ 0.02) for all 5 operations, and for all secondary outcomes after coarctation or interrupted arch with VSD repair and Norwood (p ≤ 0.03). Outcomes for RLS 1 versus 2 did not differ consistently. RLS alone explained 5% (tetralogy of Fallot repair) to 20% (Norwood) of variation in the primary outcome.
CONCLUSIONS
Adjusting for pre-operative factors, residual lesions after congenital cardiac surgery impacted in-hospital outcomes across operative complexity with greatest impact following complex operations. Minor residual lesions had minimal impact. These findings may provide guidance for surgeons when considering short-term risks and benefits of returning to bypass to repair residual lesions.

Identifiants

pubmed: 33985683
pii: S0735-1097(21)01064-0
doi: 10.1016/j.jacc.2021.03.304
pmc: PMC8245007
mid: NIHMS1695347
pii:
doi:

Types de publication

Journal Article Multicenter Study Observational Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

2382-2394

Subventions

Organisme : NHLBI NIH HHS
ID : UG1 HL135665
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL135666
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL109818
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL109741
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL135680
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL109781
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL109743
Pays : United States
Organisme : NHLBI NIH HHS
ID : U24 HL135691
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL068270
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL068270
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL109778
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL133454
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL135646
Pays : United States
Organisme : NHLBI NIH HHS
ID : UG1 HL135685
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL109816
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL109673
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL119600
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 American College of Cardiology Foundation. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures This study was supported by grants (U24HL135691, U10HL068270, HL109818, HL109778, HL109816, HL109743, HL109741, HL109673, HL068270, HL109781, HL135665, HL135680) from the National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health (NIH). Drs. Nathan and Anderson were supported by K23 grants (NHLBI/NIH HL119600and HL133454, respectively). The views expressed in this paper are those of the authors and do not necessarily represent the views of the NHLBI, NIH, or U.S. Department of Health and Human Services. The authors have reported that they have no relationships relevant to the contents of this paper to disclose.

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Auteurs

Meena Nathan (M)

Department of Cardiac Surgery, Boston Children's Hospital, Boston, Massachusetts, USA; Department of Surgery, Harvard Medical School, Boston, Massachusetts, USA. Electronic address: meena.nathan@cardio.chboston.org.

Jami C Levine (JC)

Department of Cardiology, Boston Children's Hospital, Boston, Massachusetts, USA; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.

Maria I Van Rompay (MI)

HealthCore, New England Research Institutes, Watertown, Massachusetts, USA.

Linda M Lambert (LM)

Division of Pediatric Cardiology, Primary Children's Hospital, University of Utah, Salt Lake City, Utah, USA.

Felicia L Trachtenberg (FL)

HealthCore, New England Research Institutes, Watertown, Massachusetts, USA.

Steven D Colan (SD)

Department of Cardiology, Boston Children's Hospital, Boston, Massachusetts, USA; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.

Iki Adachi (I)

Division of Congenital Heart Surgery, Texas Children's Hospital, Houston, Texas, USA.

Brett R Anderson (BR)

Division of Pediatric Cardiology, NewYork-Presbyterian/Morgan Stanley Children's Hospital, Columbia University Irving Medical Center, New York, New York, USA.

Emile A Bacha (EA)

Division of Cardiothoracic Surgery, NewYork-Presbyterian/Morgan Stanley Children's Hospital, Columbia University Irving Medical Center, New York, New York, USA.

Aaron Eckhauser (A)

Division of Pediatric Cardiothoracic Surgery, Primary Children's Hospital, University of Utah, Salt Lake City, Utah, USA.

J William Gaynor (JW)

Division of Cardiac Surgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

Eric M Graham (EM)

Division of Pediatric Cardiology, Medical University of South Carolina, Charleston, South Carolina, USA.

Benjamin Goot (B)

Division of Pediatric Cardiology, Children's Wisconsin, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

Jeffrey P Jacobs (JP)

Division of Cardiac Surgery, Johns Hopkins All Children's Hospital, St. Petersburg, Florida, USA; Division of Thoracic and Cardiovascular Surgery, Department of Surgery, University of Florida, Gainesville, Florida, USA.

Rija John (R)

Division of Congenital Heart Surgery, Texas Children's Hospital, Houston, Texas, USA.

Jonathan R Kaltman (JR)

Division of Cardiovascular Sciences, National Heart, Lung, and Blood Institute, Bethesda, Maryland, USA.

Kirk R Kanter (KR)

Division of Pediatric Cardiac Surgery, Emory University School of Medicine, Atlanta, Georgia, USA.

Carlos M Mery (CM)

Texas Center for Pediatric and Congenital Heart Disease, Dell Children's Medical Center, University of Texas Dell Medical School, Austin, Texas, USA.

L LuAnn Minich (L)

Division of Pediatric Cardiology, Primary Children's Hospital, University of Utah, Salt Lake City, Utah, USA.

Richard Ohye (R)

Division of Pediatric Cardiac Surgery, C.S. Mott Children's Hospital, Ann Arbor, Michigan, USA.

David Overman (D)

Division of Cardiovascular Surgery, Children's Minnesota, Mayo Clinic-Children's Minnesota Cardiovascular Collaborative, Minneapolis, Minnesota, USA.

Christian Pizarro (C)

Division of Cardiac Surgery, Nemours Cardiac Center, Alfred I duPont Hospital for Children, Wilmington, Delaware, USA.

Geetha Raghuveer (G)

Heart Center, Children's Mercy Hospital, Kansas City, Missouri, USA.

Marcus S Schamberger (MS)

Division of Pediatric Cardiology, Riley Hospital for Children, Indiana University, Indianapolis, Indiana, USA.

Steven M Schwartz (SM)

Division of Cardiac Critical Care Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.

Shanthi L Narasimhan (SL)

Division of Pediatric Cardiology, Masonic Children's Hospital, Minneapolis, Minnesota, USA.

Michael D Taylor (MD)

Division of Pediatric Cardiology, Cincinnati Children's Hospital and Medical Center, Cincinnati, Ohio, USA.

Ke Wang (K)

HealthCore, New England Research Institutes, Watertown, Massachusetts, USA.

Jane W Newburger (JW)

Department of Cardiology, Boston Children's Hospital, Boston, Massachusetts, USA; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.

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