Heterotaxy Adverse Long-Term Outcomes After Fontan Completion

被引:21
作者
Marathe, Supreet P. [1 ,2 ]
Zannino, Diana [3 ]
Cao, Jacob Y. [4 ,5 ]
du Plessis, Karin [3 ,6 ]
Marathe, Shilpa S. [1 ]
Ayer, Julian [7 ,8 ,9 ]
Celermajer, David S. [4 ,5 ]
Gentles, Thomas L. [11 ]
Sholler, Gary F. [7 ,8 ,9 ]
Justo, Robert N. [1 ,2 ]
Alphonso, Nelson [1 ,2 ]
d'Udekem, Yves [3 ,6 ,10 ]
Winlaw, David S. [7 ]
机构
[1] Queensland Childrens Hosp, Queensland Pediat Cardiac Serv, Brisbane, Qld, Australia
[2] Univ Queensland, Brisbane, Qld, Australia
[3] Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[4] Univ Sydney, Sydney Med Sch, Sydney, NSW, Australia
[5] Royal Prince Alfred Hosp, Dept Cardiol, Sydney, NSW, Australia
[6] Univ Melbourne, Fac Med, Dept Pediat, Melbourne, Vic, Australia
[7] Childrens Hosp Westmead, Heart Ctr Children, Cnr Hawkesbury Rd & Hainsworth St, Westmead, NSW 2145, Australia
[8] Univ Sydney, Discipline Child & Adolescent Hlth, Sydney Med Sch, Fac Hlth & Med, Sydney, NSW, Australia
[9] Sydney Childrens Hosp, Network Cardiac Serv, Sydney, NSW, Australia
[10] Royal Childrens Hosp, Dept Cardiac Surg, Melbourne, Vic, Australia
[11] Starship Childrens Hosp, Starship Green Lane Pediat & Congenital Cardiac S, Auckland, New Zealand
基金
英国医学研究理事会;
关键词
FUNCTIONAL SINGLE VENTRICLE; ATRIAL ISOMERISM; FOLLOW-UP; OPERATION; SURVIVAL; PALLIATION; EXPERIENCE; MANAGEMENT;
D O I
10.1016/j.athoracsur.2019.11.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Heterotaxy is considered a risk factor for poor outcomes after the Fontan operation. However, longterm data to support this notion are lacking. The aims of this study were to ascertain the long-term outcomes of patients with heterotaxy after hospital discharge after Fontan completion and to compare these outcomes with those of a contemporary nonheterotaxy cohort. Methods. A binational Fontan registry (n = 1540) was analyzed to identify patients with heterotaxy and compare them with patients without heterotaxy. The primary composite end point was Fontan failure, encompassing death, heart transplantation, Fontan take-down or conversion, protein-losing enteropathy, plastic bronchitis, or New York Heart Association functional class III or IV. Results. A total of 109 patients with heterotaxy were identified and they were compared with 1431 nonheterotaxy patients after Fontan completion. There was no difference in unadjusted 15-year freedom from Fontan failure (heterotaxy, 78% vs nonheterotaxy, 85%; P = .2). Patients in the heterotaxy group had a significantly higher cumulative incidence of post- Fontan arrhythmias (P <.001). Propensity-score matching for confounders yielded 73 patients with heterotaxy matched with 439 patients without heterotaxy, in whom 15-year freedom from Fontan failure was also not different (heterotaxy, 76% vs nonheterotaxy, 81%; P = .2). There was no difference in 15-year freedom from Fontan failure in patients with right vs left isomerism (right isomerism, 80% vs left isomerism, 76%; P = .7). Conclusions. Although heterotaxy may complicate the pre-Fontan course, once the Fontan procedure is successfully completed, heterotaxy does not appear to be an important risk factor for Fontan failure. Patients with heterotaxy are at a higher risk of post-Fontan arrhythmias compared with patients without heterotaxy. (C) 2020 by The Society of Thoracic Surgeons.
引用
收藏
页码:646 / 653
页数:8
相关论文
共 20 条
[1]   Outcomes of multistage palliation of infants with functional single ventricle and heterotaxy syndrome [J].
Alsoufi, Bahaaldin ;
McCracken, Courtney ;
Schlosser, Brian ;
Sachdeva, Ritu ;
Well, Andrew ;
Kogon, Brian ;
Border, William ;
Kanter, Kirk .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2016, 151 (05) :1369-+
[2]   Improving outcomes of the Fontan operation in children with atrial isomerism and heterotaxy syndromes [J].
Azakie, A ;
Merklinger, SL ;
Williams, WG ;
Van Arsdell, GS ;
Coles, JG ;
Adatia, I .
ANNALS OF THORACIC SURGERY, 2001, 72 (05) :1636-1640
[3]   Early and late results of the modified Fontan operation for heterotaxy syndrome - 30 years of experience in 142 patients [J].
Bartz, Peter J. ;
Driscoll, David J. ;
Dearani, Joseph A. ;
Puga, Francisco J. ;
Danielson, Gordon K. ;
O'Leary, Patrick W. ;
Earing, Michael G. ;
Warnes, Carole A. ;
Hodge, David O. ;
Cetta, Frank .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2006, 48 (11) :2301-2305
[4]   Survival into adulthood of patients with atrial isomerism undergoing cardiac surgery [J].
Bhaskar, Jayapadman ;
Galati, John C. ;
Brooks, Paul ;
Oppido, Guido ;
Konstantinov, Igor E. ;
Brizard, Christian P. ;
d'Udekem, Yves .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2015, 149 (06) :1509-1513
[5]   Long-term outcomes after first-onset arrhythmia in Fontan physiology [J].
Carins, Thomas A. ;
Shi, William Y. ;
Iyengar, Ajay J. ;
Nisbet, Ashley ;
Forsdick, Victoria ;
Zannino, Diana ;
Gentles, Thomas ;
Radford, Dorothy J. ;
Justo, Robert ;
Celermajer, David S. ;
Bullock, Andrew ;
Winlaw, David ;
Wheaton, Gavin ;
Grigg, Leeanne ;
d'Udekem, Yves .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2016, 152 (05) :1355-1361
[6]   Predictors of Survival After Single-Ventricle Palliation The Impact of Right Ventricular Dominance [J].
d'Udekem, Yves ;
Xu, Mary Y. ;
Galati, John C. ;
Lu, Siming ;
Iyengar, Ajay J. ;
Konstantinov, Igor E. ;
Wheaton, Gavin R. ;
Ramsay, James M. ;
Grigg, Leeanne E. ;
Millar, Johnny ;
Cheung, Michael M. ;
Brizard, Christian P. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2012, 59 (13) :1178-1185
[7]   Long-term survival after the Fontan operation: Twenty years of experience at a single center [J].
Downing, Tacy E. ;
Allen, Kiona Y. ;
Glatz, Andrew C. ;
Rogers, Lindsay S. ;
Ravishankar, Chitra ;
Rychik, Jack ;
Faerber, Jennifer A. ;
Fuller, Stephanie ;
Montenegro, Lisa M. ;
Steven, James M. ;
Spray, Thomas L. ;
Nicolson, Susan C. ;
Gaynor, J. William ;
Goldberg, David J. .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2017, 154 (01) :243-+
[8]   5-YEAR TO 15-YEAR FOLLOW-UP AFTER FONTAN OPERATION [J].
DRISCOLL, DJ ;
OFFORD, KP ;
FELDT, RH ;
SCHAFF, HV ;
PUGA, FJ ;
DANIELSON, GK .
CIRCULATION, 1992, 85 (02) :469-496
[9]   The Australia and New Zealand Fontan Registry: description and initial results from the first population-based Fontan registry [J].
Iyengar, A. J. ;
Winlaw, D. S. ;
Galati, J. C. ;
Gentles, T. L. ;
Weintraub, R. G. ;
Justo, R. N. ;
Wheaton, G. R. ;
Bullock, A. ;
Celermajer, D. S. ;
d'Udekem, Y. .
INTERNAL MEDICINE JOURNAL, 2014, 44 (02) :148-155
[10]   Surgical Management of the Neonate With Heterotaxy and Long-Term Outcomes of Heterotaxy [J].
Jonas, Richard A. .
WORLD JOURNAL FOR PEDIATRIC AND CONGENITAL HEART SURGERY, 2011, 2 (02) :264-274