Contemporary management of right atrial isomerism: Effect of evolving therapeutic strategies

被引:40
作者
Yun, TJ
Al-Radi, OO
Adatia, I
Caldarone, CA
Coles, JG
Williams, WG
Smallhorn, J
Van Arsdell, GS
机构
[1] Hosp Sick Children, Div Cardiovasc Surg, Cardiac Program, Toronto, ON M5G 1X8, Canada
[2] Univ Ulsan, Asan Med Ctr, Div Pediat Cardiac Surg, Ulsan 680749, South Korea
[3] Univ Calif San Francisco, Div Pediat Cardiol, San Francisco, CA 94143 USA
关键词
D O I
10.1016/j.jtcvs.2005.11.036
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Infants with right atrial isomerism have poor outcomes because of a complex combination of cardiac anomalies. Aggressive management of total anomalous pulmonary venous drainage might have a positive effect on the prognosis. Methods: Outcomes of all children with right atrial isomerism from 1994 to the present were reviewed. Management of total anomalous pulmonary venous drainage evolved from no repair or conventional surgical technique to primary sutureless repair on initial palliation. Cox survival models were used to identify variables associated with reduced survival. Results: There were 55 children enrolled in the study. The median age at the initial visit was 2 days. Fifty-one patients had total anomalous pulmonary venous drainage ( obstructive in 22 patients). Withdrawal of treatment occurred in 11 (20%) of 55 patients during an interval of institutional bias toward no treatment. Thirteen (24%) of 55 patients had palliations without total anomalous pulmonary venous drainage repair, and 3 (23%) of 13 survived. Thirty-one (56%) of 55 patients had operations that included total anomalous pulmonary venous drainage repair, of whom 13 (42%) of 31 underwent primary sutureless repair for total anomalous pulmonary venous drainage. Sixteen (52%) of 31 survived, and their current status 1 to 10 years (median, 5.8 years) after repair is post-Fontan (7/16 [44%]), postbidirectional Glenn (6/16 [38%]), and others (3 [ 20%]). In patients who underwent total anomalous pulmonary venous drainage repair (n=31), 2 risk factors of decreased survival were identified: drainage site obstruction and infracardiac or mixed-type total anomalous pulmonary venous drainage. After adjustment, sutureless repair appeared to be associated with improved survival (hazard ratio, 0.43), but this beneficial effect did not reach significance (P=.19). Conclusions: Mortality continues to be high; however, aggressive total anomalous pulmonary venous drainage repair for right atrial isomerism has resulted in improved survival. The role of primary sutureless repair for total anomalous pulmonary venous drainage remains to be defined.
引用
收藏
页码:1108 / 1113
页数:6
相关论文
共 30 条
[1]   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
[2]  
Bando K, 1996, CIRCULATION, V94, P12
[3]  
CALDARONE CA, 2004, SUTURLESS PULMONARY
[4]  
CAROTTI A, 1995, J THORAC CARDIOV SUR, V110, P1151, DOI 10.1016/S0022-5223(05)80190-4
[5]   Outcome of infants with right atrial isomerism: is prognosis better with normal pulmonary venous drainage? [J].
Cheung, YF ;
Cheng, VYW ;
Chau, AKT ;
Chiu, CSW ;
Yung, TC ;
Leung, MP .
HEART, 2002, 87 (02) :146-152
[6]  
DETOMMASI SM, 1981, BRIT HEART J, V45, P236
[7]  
DIDONATO R, 1987, ANN THORAC SURG, V44, P35
[8]   Total anomalous pulmonary venous connections and consideration of the Fontan or one-ventricle repair [J].
Freedom, RM ;
Hashmi, A .
ANNALS OF THORACIC SURGERY, 1998, 66 (02) :681-682
[9]   Outcomes of left atrial isomerism over a a 28-year period at a single institution [J].
Gilljam, T ;
McCrindle, BW ;
Smallhorn, JF ;
Williams, WG ;
Freedom, RM .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 36 (03) :908-916
[10]   Management and outcomes of right atrial isomerism: A 26-year experience [J].
Hashmi, A ;
Abu-Sulaiman, R ;
McCrindle, BW ;
Smallhorn, JF ;
Williams, WG ;
Freedom, RM .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1998, 31 (05) :1120-1126