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Erschienen in: Pediatric Cardiology 4/2021

29.01.2021 | Original Article

Survival Outcomes of Two-Stage Intracardiac Repair in Large Ventricular Septal Defect and Trisomy 18

verfasst von: Ryosuke Nakai, Tao Fujioka, Kenichi Okamura, Toshihiko Suzuki, Atsushi Nakao, Jotaro Kobayashi, Keiji Tsuchiya

Erschienen in: Pediatric Cardiology | Ausgabe 4/2021

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Abstract

Background

Surgical management has not been encouraged in patients with trisomy 18 (T18) and congenital heart diseases due to poor survival. This study aimed to investigate (1) the appropriateness of palliative surgeries followed by intracardiac repair (ICR) (i.e., two-stage ICR) for patients with a large ventricular septal defect (VSD) and T18, and (2) its impact on their long-term outcomes.

Methods

Medical charts of patients with VSD and T18 who underwent two-stage ICR at the Japanese Red Cross Medical Center between January 2005 and December 2019 were retrospectively reviewed. Demographic data, timing, and types of palliative surgeries, information related to ICR, peri- and postoperative clinical information, postoperative survival, and cause of death were collected. The long-term prognosis of patients treated with two-stage ICR was compared with that of patients treated with primary ICR and palliative surgery without ICR.

Results

Overall, 18 (2 male, 16 female) patients underwent two-stage ICR. Pulmonary artery banding was the initial palliative surgery in all patients after a median duration of 19.5 (range 6–194) days of life. The median age and the mean body weight at the time of ICR were 18.2 (7.6–50.7) months and 6.0 ± 1.0 kg, respectively. The mean pulmonary artery pressure and pulmonary vascular resistance index before ICR were 19.1 ± 7.3 mmHg and 3.4 ± 2.0 U m2, respectively. Overall, 17/18 (94%) patients were discharged after ICR. Fourteen (78%) patients were alive during data collection. None of the patients died of cardiac insufficiency, and the median duration of survival was 46.3 (14.3–186.4) months since birth. Most patients required cardiac medications rather than pulmonary vasodilators at the last follow-up. During the study period, three patients underwent primary ICR, and 46 underwent palliative surgery without ICR. Of those who underwent primary ICR, two died in the hospital on the first and 48th day following ICR, and the third died 179 days after the ICR. The Log-rank test revealed a significantly longer survival for the patients treated with two-stage ICR compared with those treated with palliative surgery without ICR (P = 0.003).

Conclusion

Two-stage ICR improves the long-term survival of patients with VSDs and T18. This safe surgical strategy can also prevent pulmonary hypertension in such patients.
Literatur
1.
Zurück zum Zitat Bruns DA, Martinez A (2016) An analysis of cardiac defects and surgical interventions in 84 cases with full trisomy 18. Am J Med Genet A 170A:337–343CrossRef Bruns DA, Martinez A (2016) An analysis of cardiac defects and surgical interventions in 84 cases with full trisomy 18. Am J Med Genet A 170A:337–343CrossRef
2.
Zurück zum Zitat Carter PE, Pearn JH, Bell J, Martin N, Anderson NG (1985) Survival in trisomy 18. Life tables for use in genetic counselling and clinical paediatrics. Clin Genet 27:59–61CrossRef Carter PE, Pearn JH, Bell J, Martin N, Anderson NG (1985) Survival in trisomy 18. Life tables for use in genetic counselling and clinical paediatrics. Clin Genet 27:59–61CrossRef
3.
Zurück zum Zitat Goldstein H, Nielsen KG (1988) Rates and survival of individuals with trisomy 13 and 18. Data from a 10-year period in Denmark. Clin Genet 34:366–372CrossRef Goldstein H, Nielsen KG (1988) Rates and survival of individuals with trisomy 13 and 18. Data from a 10-year period in Denmark. Clin Genet 34:366–372CrossRef
4.
Zurück zum Zitat Rasmussen SA, Wong LY, Yang Q, May KM, Friedman JM (2003) Population-based analyses of mortality in trisomy 13 and trisomy 18. Pediatrics 111:777–784CrossRef Rasmussen SA, Wong LY, Yang Q, May KM, Friedman JM (2003) Population-based analyses of mortality in trisomy 13 and trisomy 18. Pediatrics 111:777–784CrossRef
5.
Zurück zum Zitat Kosho T, Kuniba H, Tanikawa Y, Hashimoto Y, Sakurai H (2013) Natural history and parental experience of children with trisomy 18 based on a questionnaire given to a Japanese trisomy 18 parental support group. Am J Med Genet A 161A:1531–1542CrossRef Kosho T, Kuniba H, Tanikawa Y, Hashimoto Y, Sakurai H (2013) Natural history and parental experience of children with trisomy 18 based on a questionnaire given to a Japanese trisomy 18 parental support group. Am J Med Genet A 161A:1531–1542CrossRef
6.
Zurück zum Zitat Kaneko Y, Kobayashi J, Yamamoto Y, Yoda H, Kanetaka Y, Nakajima Y, Endo D, Tsuchiya K, Sato H, Kawakami T (2008) Intensive cardiac management in patients with trisomy 13 or trisomy 18. Am J Med Genet A 146A:1372–1380CrossRef Kaneko Y, Kobayashi J, Yamamoto Y, Yoda H, Kanetaka Y, Nakajima Y, Endo D, Tsuchiya K, Sato H, Kawakami T (2008) Intensive cardiac management in patients with trisomy 13 or trisomy 18. Am J Med Genet A 146A:1372–1380CrossRef
7.
Zurück zum Zitat Kaneko Y, Kobayashi J, Achiwa I, Yoda H, Tsuchiya K, Nakajima Y, Endo D, Sato H, Kawakami T (2009) Cardiac surgery in patients with trisomy 18. Pediatr Cardiol 30:729–734CrossRef Kaneko Y, Kobayashi J, Achiwa I, Yoda H, Tsuchiya K, Nakajima Y, Endo D, Sato H, Kawakami T (2009) Cardiac surgery in patients with trisomy 18. Pediatr Cardiol 30:729–734CrossRef
8.
Zurück zum Zitat Kobayashi J, Kaneko Y, Yamamoto Y, Yoda H, Tsuchiya K (2010) Radical surgery for a ventricular septal defect associated with trisomy 18. Gen Thorac Cardiovasc Surg 58:223–227CrossRef Kobayashi J, Kaneko Y, Yamamoto Y, Yoda H, Tsuchiya K (2010) Radical surgery for a ventricular septal defect associated with trisomy 18. Gen Thorac Cardiovasc Surg 58:223–227CrossRef
9.
Zurück zum Zitat Van Praagh S, Truman T, Firpo A, Bang-Rodrigo A, Fried R, McManus B, Engle MA, Van Praagh R (1989) Cardiac malformations in trisomy-18: a study of 41 postmortem cases. J Am Coll Cardiol 13:1586–1597CrossRef Van Praagh S, Truman T, Firpo A, Bang-Rodrigo A, Fried R, McManus B, Engle MA, Van Praagh R (1989) Cardiac malformations in trisomy-18: a study of 41 postmortem cases. J Am Coll Cardiol 13:1586–1597CrossRef
10.
Zurück zum Zitat Musewe NN, Alexander DJ, Teshima I, Smallhorn JF, Freedom RM (1990) Echocardiographic evaluation of the spectrum of cardiac anomalies associated with trisomy 13 and trisomy 18. J Am Coll Cardiol 15:673–677CrossRef Musewe NN, Alexander DJ, Teshima I, Smallhorn JF, Freedom RM (1990) Echocardiographic evaluation of the spectrum of cardiac anomalies associated with trisomy 13 and trisomy 18. J Am Coll Cardiol 15:673–677CrossRef
11.
Zurück zum Zitat Embleton ND, Wyllie JP, Wright MJ, Burn J, Hunter S (1996) Natural history of trisomy 18. Arch Dis Child Fetal Neonatal Ed 75:F38-41CrossRef Embleton ND, Wyllie JP, Wright MJ, Burn J, Hunter S (1996) Natural history of trisomy 18. Arch Dis Child Fetal Neonatal Ed 75:F38-41CrossRef
12.
Zurück zum Zitat Kosho T, Nakamura T, Kawame H, Baba A, Tamura M, Fukushima Y (2006) Neonatal management of trisomy 18: clinical details of 24 patients receiving intensive treatment. Am J Med Genet A 140:937–944CrossRef Kosho T, Nakamura T, Kawame H, Baba A, Tamura M, Fukushima Y (2006) Neonatal management of trisomy 18: clinical details of 24 patients receiving intensive treatment. Am J Med Genet A 140:937–944CrossRef
13.
Zurück zum Zitat Graham EM, Bradley SM, Shirali GS, Hills CB, Atz AM, Pediatric Cardiac Care C (2004) Effectiveness of cardiac surgery in trisomies 13 and 18 (from the Pediatric Cardiac Care Consortium). Am J Cardiol 93:801–803CrossRef Graham EM, Bradley SM, Shirali GS, Hills CB, Atz AM, Pediatric Cardiac Care C (2004) Effectiveness of cardiac surgery in trisomies 13 and 18 (from the Pediatric Cardiac Care Consortium). Am J Cardiol 93:801–803CrossRef
14.
Zurück zum Zitat Yates AR, Hoffman TM, Shepherd E, Boettner B, McBride KL (2011) Pediatric sub-specialist controversies in the treatment of congenital heart disease in trisomy 13 or 18. J Genet Couns 20:495–509CrossRef Yates AR, Hoffman TM, Shepherd E, Boettner B, McBride KL (2011) Pediatric sub-specialist controversies in the treatment of congenital heart disease in trisomy 13 or 18. J Genet Couns 20:495–509CrossRef
15.
Zurück zum Zitat Peterson JK, Kochilas LK, Catton KG, Moller JH, Setty SP (2017) Long-term outcomes of children with trisomy 13 and 18 after congenital heart disease interventions. Ann Thorac Surg 103:1941–1949CrossRef Peterson JK, Kochilas LK, Catton KG, Moller JH, Setty SP (2017) Long-term outcomes of children with trisomy 13 and 18 after congenital heart disease interventions. Ann Thorac Surg 103:1941–1949CrossRef
16.
Zurück zum Zitat McGraw MP, Perlman JM (2008) Attitudes of neonatologists toward delivery room management of confirmed trisomy 18: potential factors influencing a changing dynamic. Pediatrics 121:1106–1110CrossRef McGraw MP, Perlman JM (2008) Attitudes of neonatologists toward delivery room management of confirmed trisomy 18: potential factors influencing a changing dynamic. Pediatrics 121:1106–1110CrossRef
17.
Zurück zum Zitat Janvier A, Farlow B, Barrington K (2016) Cardiac surgery for children with trisomies 13 and 18: where are we now? Semin Perinatol 40:254–260CrossRef Janvier A, Farlow B, Barrington K (2016) Cardiac surgery for children with trisomies 13 and 18: where are we now? Semin Perinatol 40:254–260CrossRef
18.
Zurück zum Zitat Graham EM (2016) Infants with trisomy 18 and complex congenital heart defects should not undergo open heart surgery. J Law Med Ethics 44:286–291CrossRef Graham EM (2016) Infants with trisomy 18 and complex congenital heart defects should not undergo open heart surgery. J Law Med Ethics 44:286–291CrossRef
19.
Zurück zum Zitat Peterson R, Calamur N, Fiore A, Huddleston C, Spence K (2018) Factors influencing outcomes after cardiac intervention in infants with trisomy 13 and 18. Pediatr Cardiol 39:140–147CrossRef Peterson R, Calamur N, Fiore A, Huddleston C, Spence K (2018) Factors influencing outcomes after cardiac intervention in infants with trisomy 13 and 18. Pediatr Cardiol 39:140–147CrossRef
20.
Zurück zum Zitat Maeda J, Yamagishi H, Furutani Y, Kamisago M, Waragai T, Oana S, Kajino H, Matsuura H, Mori K, Matsuoka R, Nakanishi T (2011) The impact of cardiac surgery in patients with trisomy 18 and trisomy 13 in Japan. Am J Med Genet A 155A:2641–2646CrossRef Maeda J, Yamagishi H, Furutani Y, Kamisago M, Waragai T, Oana S, Kajino H, Matsuura H, Mori K, Matsuoka R, Nakanishi T (2011) The impact of cardiac surgery in patients with trisomy 18 and trisomy 13 in Japan. Am J Med Genet A 155A:2641–2646CrossRef
21.
Zurück zum Zitat Muneuchi J, Yamamoto J, Takahashi Y, Watanabe M, Yuge T, Ohno T, Imoto Y, Sese A, Joo K (2011) Outcomes of cardiac surgery in trisomy 18 patients. Cardiol Young 21:209–215CrossRef Muneuchi J, Yamamoto J, Takahashi Y, Watanabe M, Yuge T, Ohno T, Imoto Y, Sese A, Joo K (2011) Outcomes of cardiac surgery in trisomy 18 patients. Cardiol Young 21:209–215CrossRef
22.
Zurück zum Zitat Costello JP, Weiderhold A, Louis C, Shaughnessy C, Peer SM, Zurakowski D, Jonas RA, Nath DS (2015) A contemporary, single-institutional experience of surgical versus expectant management of congenital heart disease in trisomy 13 and 18 patients. Pediatr Cardiol 36:987–992CrossRef Costello JP, Weiderhold A, Louis C, Shaughnessy C, Peer SM, Zurakowski D, Jonas RA, Nath DS (2015) A contemporary, single-institutional experience of surgical versus expectant management of congenital heart disease in trisomy 13 and 18 patients. Pediatr Cardiol 36:987–992CrossRef
23.
Zurück zum Zitat Nakai Y, Asano M, Nomura N, Matsumae H, Mishima A (2016) Effectiveness of cardiac surgery in patients with trisomy 18: a single-institutional experience. Cardiol Young 26:1391–1396CrossRef Nakai Y, Asano M, Nomura N, Matsumae H, Mishima A (2016) Effectiveness of cardiac surgery in patients with trisomy 18: a single-institutional experience. Cardiol Young 26:1391–1396CrossRef
24.
Zurück zum Zitat Imai K, Uchiyama A, Okamura T, Ago M, Suenaga H, Sugita E, Ono H, Shuri K, Masumoto K, Totsu S, Nakanishi H, Kusuda S (2015) Differences in mortality and morbidity according to gestational ages and birth weights in infants with trisomy 18. Am J Med Genet A 167A:2610–2617CrossRef Imai K, Uchiyama A, Okamura T, Ago M, Suenaga H, Sugita E, Ono H, Shuri K, Masumoto K, Totsu S, Nakanishi H, Kusuda S (2015) Differences in mortality and morbidity according to gestational ages and birth weights in infants with trisomy 18. Am J Med Genet A 167A:2610–2617CrossRef
25.
Zurück zum Zitat Friedberg MK, Cho MY, Li J, Assad RS, Sun M, Rohailla S, Honjo O, Apitz C, Redington AN (2013) Adverse biventricular remodeling in isolated right ventricular hypertension is mediated by increased transforming growth factor-beta1 signaling and is abrogated by angiotensin receptor blockade. Am J Respir Cell Mol Biol 49:1019–1028CrossRef Friedberg MK, Cho MY, Li J, Assad RS, Sun M, Rohailla S, Honjo O, Apitz C, Redington AN (2013) Adverse biventricular remodeling in isolated right ventricular hypertension is mediated by increased transforming growth factor-beta1 signaling and is abrogated by angiotensin receptor blockade. Am J Respir Cell Mol Biol 49:1019–1028CrossRef
26.
Zurück zum Zitat Meyer RE, Liu G, Gilboa SM, Ethen MK, Aylsworth AS, Powell CM, Flood TJ, Mai CT, Wang Y, Canfield MA, National Birth Defects Prevention N (2016) Survival of children with trisomy 13 and trisomy 18: a multi-state population-based study. Am J Med Genet A 170A:825–837CrossRef Meyer RE, Liu G, Gilboa SM, Ethen MK, Aylsworth AS, Powell CM, Flood TJ, Mai CT, Wang Y, Canfield MA, National Birth Defects Prevention N (2016) Survival of children with trisomy 13 and trisomy 18: a multi-state population-based study. Am J Med Genet A 170A:825–837CrossRef
Metadaten
Titel
Survival Outcomes of Two-Stage Intracardiac Repair in Large Ventricular Septal Defect and Trisomy 18
verfasst von
Ryosuke Nakai
Tao Fujioka
Kenichi Okamura
Toshihiko Suzuki
Atsushi Nakao
Jotaro Kobayashi
Keiji Tsuchiya
Publikationsdatum
29.01.2021
Verlag
Springer US
Erschienen in
Pediatric Cardiology / Ausgabe 4/2021
Print ISSN: 0172-0643
Elektronische ISSN: 1432-1971
DOI
https://doi.org/10.1007/s00246-021-02546-9

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