Operative and nonoperative outcomes in patients with trisomy 13 and 18 with congenital heart disease

被引:0
作者
Greene, Christina L. [1 ]
Schulz, Antonia [1 ]
Chavez, Mariana [1 ]
Staffa, Steven J. [2 ]
Zurakowski, David [2 ]
Friedman, Kevin G. [3 ]
Emani, Sitaram M. [1 ]
Baird, Christopher W. [1 ]
机构
[1] Harvard Med Sch, Boston Childrens Hosp, Dept Cardiac Surg, Boston, MA USA
[2] Harvard Med Sch, Dept Anesthesiol Crit Care & Pain Med, Boston Childrens Hosp, Boston, MA USA
[3] Harvard Med Sch, Boston Childrens Hosp, Dept Cardiol, Boston, MA USA
来源
JTCVS OPEN | 2024年 / 20卷
关键词
trisomy; 13; 18; congenital heart disease; CARDIAC-SURGERY; NATURAL-HISTORY; MANAGEMENT; INFANTS; CHILDREN; CARE;
D O I
10.1016/j.xjon.2024.06.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate the short- and long-term outcomes of cardiac repair versus nonoperative management in patients with trisomy 13 and trisomy 18 with congenital heart disease. Methods: An institutional review board-approved, retrospective review was undertaken to identify all patients admitted with trisomy 13/18 and congenital heart disease. Patients were divided into 2 cohorts (operated vs nonoperated) and compared. Results: Between 1985 and 2023, 62 patients (34 operated and 28 nonoperated) with trisomy 13 (n = 9) and trisomy 18 (n = 53) were identified. The operated cohort was 74% girls, underwent mainly The Society of Thoracic Surgeons-European Association for Cardio-Thoracic Surgery mortality category 1 procedures (n = 24 [71%]) at a median age of 2.5 months (interquartile range [IQR], 1.3-4.5 months). This compares with the nonoperative cohort where 64% (n = 18) would have undergone The Society of Thoracic Surgeons-European Association for Cardio-Thoracic Surgery mortality category 1 procedures if surgery would have been elected. The most common diagnosis was ventricular septal defect. Postoperative median intensive care unit stay was 6.5 days (IQR, 3.7-15 days) with a total hospital length of stay of 15 days (IQR, 11-49 days). Thirty-day postoperative survival was 94%. There were 5 in-hospital deaths in the operated and 7 in the nonoperated cohort. Median follow-up was 15.4 months (IQR, 4.3-48.7 months) for the operated and 11.2 months (IQR, 1.2-48.3 months) for the nonoperated cohorts. One-year survival was 79% operated versus 51.5% nonoperated (P < .003). Nonoperative treatment had an increased risk of mortality (hazard ratio, 3.28; 95% CI, 1.46-7.4; P = .004). Conclusions: Controversy exists regarding the role of primary cardiac repair in patients with trisomy 13/18 and congenital heart disease. Cardiac repair can be performed safely with low early mortality and operated patients had higher long-term survival compared with nonoperated in our cohort.
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收藏
页码:123 / 131
页数:9
相关论文
共 24 条
  • [11] Congenital Heart Surgical Admissions in Patients with Trisomy 13 and 18: Frequency, Morbidity, and Mortality
    Ma, Michael H.
    He, Wei
    Benavidez, Oscar J.
    [J]. PEDIATRIC CARDIOLOGY, 2019, 40 (03) : 595 - 601
  • [12] The Impact of Cardiac Surgery in Patients with Trisomy 18 and Trisomy 13 in Japan
    Maeda, Jun
    Yamagishi, Hiroyuki
    Furutani, Yoshiyuki
    Kamisago, Mitsuhiro
    Waragai, Tadashi
    Oana, Shinji
    Kajino, Hiroki
    Matsuura, Hiroyuki
    Mori, Katsuhiko
    Matsuoka, Rumiko
    Nakanishi, Toshio
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2011, 155A (11) : 2641 - 2646
  • [13] CONGENITAL HEART ANOMALIES IN THE TRISOMY-18 SYNDROME, WITH REFERENCE TO CONGENITAL POLYVALVULAR DISEASE
    MATSUOKA, R
    MISUGI, K
    GOTO, A
    GILBERT, EF
    ANDO, M
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 14 (04): : 657 - 668
  • [14] Attitudes of neonatologists toward delivery room management of confirmed trisomy 18: Potential factors influencing a changing dynamic
    McGraw, Melanie P.
    Perlman, Jeffrey M.
    [J]. PEDIATRICS, 2008, 121 (06) : 1106 - 1110
  • [15] Effectiveness of cardiac surgery in patients with trisomy 18: a single-institutional experience
    Nakai, Yosuke
    Asano, Miki
    Nomura, Norikazu
    Matsumae, Hidekazu
    Mishima, Akira
    [J]. CARDIOLOGY IN THE YOUNG, 2016, 26 (07) : 1391 - 1396
  • [16] Survival and Surgical Interventions for Children With Trisomy 13 and 18
    Nelson, Katherine E.
    Rosella, Laura C.
    Mahant, Sanjay
    Guttmann, Astrid
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2016, 316 (04): : 420 - 428
  • [17] Ethical considerations for cardiac surgical interventions in children with trisomy 13 and trisomy 18
    Neubauer, Kathryn
    Boss, Renee D.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2020, 184 (01) : 187 - 191
  • [18] Long-Term Outcomes of Children With Trisomy 13 and 18 After Congenital Heart Disease Interventions
    Peterson, Jennifer K.
    Kochilas, Lazaros K.
    Catton, Kirsti G.
    Moller, James H.
    Setty, Shaun P.
    [J]. ANNALS OF THORACIC SURGERY, 2017, 103 (06) : 1941 - 1949
  • [19] Factors Influencing Outcomes After Cardiac Intervention in Infants with Trisomy 13 and 18
    Peterson, Renuka
    Calamur, Nandini
    Fiore, Andrew
    Huddleston, Charles
    Spence, Kimberly
    [J]. PEDIATRIC CARDIOLOGY, 2018, 39 (01) : 140 - 147
  • [20] Congenital malformations among liveborn infants with trisomies 18 and 13
    Pont, Stephen J.
    Robbins, James M.
    Bird, T. M.
    Gibson, James B.
    Cleves, Mario A.
    Tilford, John M.
    Aitken, Mary E.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (16) : 1749 - 1756