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J Am Coll Cardiol, 2001; 38:1181-1187 © 2001 by the American College of Cardiology Foundation |



* Department of Pediatrics, Dartmouth Medical School, Hanover, New Hampshire, USA
Division of Pediatric Cardiology, St. Louis Childrens Hospital, St. Louis, Missouri, USA
Department of Pediatrics, Loma Linda University Childrens Hospital, Loma Linda, California, USA
Department of Cardiology, Childrens Hospital, Boston, Massachusetts, USA
|| Department of Pediatric Cardiology, Emory University School of Medicine, Atlanta, Georgia, USA
¶ Department of Medicine and Community and Family Medicine and the Center for the Evaluative Clinical Sciences, Dartmouth Medical School, Hanover, New Hampshire, USA
Manuscript received December 31, 2000; revised manuscript received June 20, 2001, accepted June 26, 2001.
Reprint requests and correspondence: Dr. Pamela C. Jenkins, Department of Pediatrics, Dartmouth Medical School, Hanover, New Hampshire 03755
pcj{at}hitchcock.org
OBJECTIVES
We sought to identify the optimal treatment strategy for hypoplastic left heart syndrome (HLHS).
BACKGROUND
Surgical treatment of HLHS involves either transplantation (Tx) or staged palliation of the native heart. Identifying the best treatment for HLHS requires integrating individual patient risk factors and center-specific data.
METHODS
Decision analysis is a modeling technique used to compare six strategies: staged surgery; Tx; stage 1 surgery as an interim to Tx; and listing for transplant for one, two, or three months before performing staged surgery if a donor is unavailable. Probabilities were derived from current literature and a dataset of 231 patients with HLHS born between 1989 and 1994. The goal was to maximize first-year survival.
RESULTS
If a donor is available within one month, Tx is the optimal choice, given baseline probabilities; if no donor is found by the end of one month, stage 1 surgery should be performed. When survival and organ donation probabilities were varied, staged surgery was the optimal choice for centers with organ donation rates <10% in three months and with stage 1 mortality <20%. Waiting one month on the transplant list optimized survival when the three-month organ donation rate was
30%. Performing stage 1 surgery before listing, or performing stage 1 surgery after an unsuccessful two- or three-month wait for transplant, were almost never optimal choices.
CONCLUSIONS
The best strategy for centers that treat patients with HLHS should be guided by local organ availability, stage 1 surgical mortality and patient risk factors.
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