Heart Transplantation in Children With a Fontan Procedure

被引:79
作者
Kanter, Kirk R. [1 ]
Mahle, William T.
Vincent, Robert N.
Berg, Alexandria M.
Kogon, Brian E.
Kirshbom, Paul M.
机构
[1] Emory Univ, Sch Med, Dept Surg, Div Cardiothorac Surg, Atlanta, GA 30322 USA
关键词
ORTHOTOPIC CARDIAC TRANSPLANTATION; PROTEIN-LOSING ENTEROPATHY; DISEASE; CIRCULATION; SURGERY; ADULTS;
D O I
10.1016/j.athoracsur.2010.11.031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Previous studies have reported that children with a prior Fontan procedure have decreased survival after heart transplantation. We examined 190 primary pediatric heart transplants. Methods. Since 1988, 27 (14.2%) of 190 children less than 18 years old undergoing primary heart transplantation had a Fontan procedure 3.7 +/- 4.3 years before transplantation. Compared with 163 (85.8%) non-Fontan primary transplants, the Fontan patients were similar in age (8.2 +/- 5.0 vs 6.5 +/- 6.0 years), presensitization, and pretransplant clinical status. More Fontan patients had prior operations (100% vs 50%; p < 0.0001) and needed pulmonary artery reconstruction (100% vs 23.5%; p < 0.0001). Twelve (44%) had protein-losing enteropathy. Results. Donor ischemic times (211 +/- 72 vs 170 +/- 61 minutes; p = 0.0018) and cardiopulmonary bypass times (197 +/- 91 vs 121 +/- 53 minutes; p < 0.0001) were greater in the Fontan group as were durations of ventilator support (4.9 +/- 6.6 vs 2.6 +/- 3.9 days; p = 0.018) and hospital stay (20.2 +/- 17.5 vs 14.3 +/- 12.4 days; p = 0.0435). The Fontan group had one 30-day mortality. One-year actuarial survival (81.5% vs 84.6%, Fontan vs non-Fontan) and five-year actuarial survival (65.5% vs 66.2%, Fontan vs non-Fontan) were similar, as was rejection incidence at one year (2.0 +/- 2.0 vs 1.7 +/- 1.9 episodes per patient; p = 0.3972). Five Fontan patients (18.5%) required retransplantation 4.9 +/- 3.6 years posttransplant compared with 18 non-Fontan patients (11.0%) retransplanted 5.2 +/- 3.4 years posttransplant (p = 0.3346). Conclusions. Contrary to prior reports, we did not identify any early or midterm disadvantage for children undergoing heart transplantation after a previous Fontan procedure despite more complex transplant operations. We contend that carefully selected children with a failing Fontan circulation can do as well as other children with heart transplantation. (Ann Thorac Surg 2011;91:823-30) (C) 2011 by The Society of Thoracic Surgeons
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收藏
页码:823 / 830
页数:8
相关论文
共 24 条
[21]  
Mitchell Max B, 2004, Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu, V7, P56, DOI 10.1053/j.pcsu.2004.02.013
[22]   Evidence of pulmonary vascular disease after heart transplantation for Fontan circulation failure [J].
Mitchell, MB ;
Campbell, DN ;
Ivy, D ;
Boucek, MM ;
Sondheimer, HM ;
Pietra, B ;
Das, BB ;
Coll, JR .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2004, 128 (05) :693-702
[23]   Surgical reinterventions following the Fontan procedure [J].
Petko, M ;
Myung, RJ ;
Wernovsky, G ;
Cohen, MI ;
Rychik, J ;
Nicolson, SC ;
Gaynor, JW ;
Spray, TL .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2003, 24 (02) :255-259
[24]   Heart transplantation after congenital heart surgery: improving results and future goals [J].
Simmonds, Jacob ;
Burch, Michael ;
Dawkins, Helen ;
Tsang, Victor .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2008, 34 (02) :313-317