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PMID: 20505177 Published · ppublish English Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural

Comparison of shunt types in the Norwood procedure for single-ventricle lesions.

The New England journal of medicine ·Vol. 362 ·No. 21 ·2010-05-27 ·Pages 1980-92

Ohye RG, Sleeper LA, Mahony L, Newburger JW, Pearson GD, Lu M, Goldberg CS, Tabbutt S, Frommelt PC, Ghanayem NS, Laussen PC, Rhodes JF, Lewis AB, Mital S, Ravishankar C, Williams IA, Dunbar-Masterson C, Atz AM, Colan S, Minich LL, Pizarro C, Kanter KR, Jaggers J, Jacobs JP, Krawczeski CD, Pike N, McCrindle BW, Virzi L, Gaynor JW, Pediatric Heart Network Investigators

Abstract

The Norwood procedure with a modified Blalock-Taussig (MBT) shunt, the first palliative stage for single-ventricle lesions with systemic outflow obstruction, is associated with high mortality. The right ventricle-pulmonary artery (RVPA) shunt may improve coronary flow but requires a ventriculotomy. We compared the two shunts in infants with hypoplastic heart syndrome or related anomalies. Infants undergoing the Norwood procedure were randomly assigned to the MBT shunt (275 infants) or the RVPA shunt (274 infants) at 15 North American centers. The primary outcome was death or cardiac transplantation 12 months after randomization. Secondary outcomes included unintended cardiovascular interventions and right ventricular size and function at 14 months and transplantation-free survival until the last subject reached 14 months of age. Transplantation-free survival 12 months after randomization was higher with the RVPA shunt than with the MBT shunt (74% vs. 64%, P=0.01). However, the RVPA shunt group had more unintended interventions (P=0.003) and complications (P=0.002). Right ventricular size and function at the age of 14 months and the rate of nonfatal serious adverse events at the age of 12 months were similar in the two groups. Data collected over a mean (+/-SD) follow-up period of 32+/-11 months showed a nonsignificant difference in transplantation-free survival between the two groups (P=0.06). On nonproportional-hazards analysis, the size of the treatment effect differed before and after 12 months (P=0.02). In children undergoing the Norwood procedure, transplantation-free survival at 12 months was better with the RVPA shunt than with the MBT shunt. After 12 months, available data showed no significant difference in transplantation-free survival between the two groups. (ClinicalTrials.gov number, NCT00115934.)

MeSH Terms
Cardiac Surgical Procedures/methods Female Follow-Up Studies Heart Bypass, Right/methods Heart Transplantation/statistics & numerical data Heart Ventricles/abnormalities,surgery Humans Hypoplastic Left Heart Syndrome/mortality,surgery Infant, Newborn Intention to Treat Analysis Kaplan-Meier Estimate Male Postoperative Complications Proportional Hazards Models Pulmonary Artery/surgery
Authors & Affiliations
30 authors, click to expand affiliations / ORCID
Ohye Richard G
University of Michigan Medical School, Ann Arbor, MI, USA. [email protected]
Sleeper Lynn A
Mahony Lynn
Newburger Jane W
Pearson Gail D
Lu Minmin
Goldberg Caren S
Tabbutt Sarah
Frommelt Peter C
Ghanayem Nancy S
Laussen Peter C
Rhodes John F
Lewis Alan B
Mital Seema
Ravishankar Chitra
Williams Ismee A
Dunbar-Masterson Carolyn
Atz Andrew M
Colan Steven
Minich L LuAnn
Pizarro Christian
Kanter Kirk R
Jaggers James
Jacobs Jeffrey P
Krawczeski Catherine Dent
Pike Nancy
McCrindle Brian W
Virzi Lisa
Gaynor J William
Pediatric Heart Network Investigators
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Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
1533-4406
Published
2010-05-27
Pages
1980-92
Language
English
Region
United States
NLM ID
0255562
PMCID
PMC2891109
Subset
IM
Grants
NHLBI NIH HHS · HL068288 · United States
NHLBI NIH HHS · U01 HL068292-08 · United States
NHLBI NIH HHS · U01 HL068281-08 · United States
NHLBI NIH HHS · HL068285 · United States
NHLBI NIH HHS · U01 HL068279-08 · United States
NHLBI NIH HHS · U01 HL068285-08 · United States
NHLBI NIH HHS · U01 HL068279 · United States
NHLBI NIH HHS · U01 HL068269-08 · United States
NHLBI NIH HHS · U01 HL068290 · United States
NHLBI NIH HHS · U10 HL068270 · United States
NHLBI NIH HHS · U01 HL068281 · United States
NHLBI NIH HHS · U01 HL068270-08 · United States
NHLBI NIH HHS · HL068290 · United States
NHLBI NIH HHS · U01 HL068290-08 · United States
NHLBI NIH HHS · U01 HL085057-03 · United States
NHLBI NIH HHS · U01 HL068269 · United States
NHLBI NIH HHS · U10 HL109816 · United States
NHLBI NIH HHS · HL068279 · United States
NHLBI NIH HHS · U01 HL068288 · United States
NHLBI NIH HHS · U01 HL068288-08 · United States
NHLBI NIH HHS · U01 HL068270 · United States
NHLBI NIH HHS · HL085057 · United States
NHLBI NIH HHS · HL068281 · United States
NHLBI NIH HHS · U01 HL068292 · United States
NHLBI NIH HHS · HL068269 · United States
NHLBI NIH HHS · HL068270 · United States
NHLBI NIH HHS · U01 HL085057 · United States
NHLBI NIH HHS · U10 HL109778 · United States
NHLBI NIH HHS · U01 HL068285 · United States
NHLBI NIH HHS · HL068292 · United States
Databases
ClinicalTrials.gov
NCT00115934
Corrections
CommentIn
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