Thorac Cardiovasc Surg 2024; 72(05): 366-374
DOI: 10.1055/a-2158-1119
Original Cardiovascular

Development of Weight and Height Age z-Score after Total Cavopulmonary Connection

Carlo Bilic*
1   Department of Congenital and Pediatric Heart surgery, German Heart Center Munich, Technische Universität München, Munich Germany, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Munich, Germany
,
Helena Staehler*
1   Department of Congenital and Pediatric Heart surgery, German Heart Center Munich, Technische Universität München, Munich Germany, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Munich, Germany
,
Carolin Niedermaier
1   Department of Congenital and Pediatric Heart surgery, German Heart Center Munich, Technische Universität München, Munich Germany, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Munich, Germany
,
Thibault Schaeffer
1   Department of Congenital and Pediatric Heart surgery, German Heart Center Munich, Technische Universität München, Munich Germany, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Munich, Germany
,
Magdalena Cuman
2   Department of Congenital Heart Disease and Pediatric Cardiology, German Heart Center Munich, Technische Universität München, Munich, Germany
,
Paul Philipp Heinisch
1   Department of Congenital and Pediatric Heart surgery, German Heart Center Munich, Technische Universität München, Munich Germany, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Munich, Germany
,
3   Department of Cardiovascular Surgery, German Heart Center Munich, Technische Universität München, Munich, Germany
,
Nicole Piber
3   Department of Cardiovascular Surgery, German Heart Center Munich, Technische Universität München, Munich, Germany
,
Alfred Hager
2   Department of Congenital Heart Disease and Pediatric Cardiology, German Heart Center Munich, Technische Universität München, Munich, Germany
,
Peter Ewert
2   Department of Congenital Heart Disease and Pediatric Cardiology, German Heart Center Munich, Technische Universität München, Munich, Germany
,
Jürgen Hörer
1   Department of Congenital and Pediatric Heart surgery, German Heart Center Munich, Technische Universität München, Munich Germany, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Munich, Germany
,
Masamichi Ono
1   Department of Congenital and Pediatric Heart surgery, German Heart Center Munich, Technische Universität München, Munich Germany, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Munich, Germany
› Author Affiliations

Abstract

Objective We aimed to analyze somatic growth of patients after total cavopulmonary connection (TCPC) as well as to identify factors influencing postoperative catch-up growth.

Methods A total of 309 patients undergoing TCPC at 4 years old or less between 1994 and 2021 were included. Weight for age z-score (WAZ) and height for age-z-score (HAZ) at TCPC and at postoperative time between 1 and 3 years were calculated. Factors influencing somatic growth were analyzed.

Results Most frequent diagnosis and initial palliation were hypoplastic left heart syndrome (HLHS) (34%) and the Norwood procedure (51%), respectively. Median age and weight at TCPC were 2.0 (IQR: 1.7–2.5) years and 11.3 (10.5–12.7) kg, respectively. Median 519 days after TCPC, a significant increase in WAZ (−0.4 to −0.2, p < 0.001) was observed, but not in HAZ (−0.6 to −0.6, p = 0.38). Older age at TCPC (p < 0.001, odds ratio [OR]: 2.6) and HLHS (p = 0.007, OR: 2.2) were risks for low WAZ after TCPC. Older age at TCPC (p = 0.009, OR: 1.9) and previous Norwood procedure (p = 0.021, OR: 2.0) were risks for low HAZ after TCPC. Previous bidirectional cavopulmonary shunt (BCPS) was a protective factor for both WAZ (p = 0.012, OR: 0.06) and HAZ (p = 0.028, OR: 0.30) at TCPC.

Conclusion In patients undergoing TCPC at the age of 4 years or less, a significant catch-up growth was observed in WAZ after TCPC, but not in HAZ. Previous BCPS resulted to be a protective factor for a better somatic development at TCPC. HLHSs undergoing Norwood were considered as risks for somatic development after TCPC.

Note

Presented at the 52nd Annual Meeting of the German Society of Thoracic and Cardiovascular Surgery, Hamburg, Germany, February 11–14, 2023.


Authors' Contribution

C.B.: conception and design of the work, data collection, analysis and interpretation of the data, drafting the manuscript. H.S.: data collection, drafting the manuscript. C.N.: data collection. T.S.: analysis and interpretation of the data, statistical analysis. M.C.: conception and design of the work. P.P.H.: analysis and interpretation of the data. M.B.: statistical analysis. N.P.: analysis and interpretation of the data. A.H.: critical revision of the manuscript. P.E.: conception and design of the work, critical revision of the manuscript. J.H.: conception and design of the work, critical revision of the manuscript. M.O.: conception and design of the work, drafting the manuscript.


* These authors contributed equally.


Supplementary Material



Publication History

Received: 13 May 2023

Accepted: 17 August 2023

Accepted Manuscript online:
22 August 2023

Article published online:
16 October 2023

© 2023. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Anderson RH, Franklin RCG, Spicer DE. Anatomy of the functionally univentricular heart. World J Pediatr Congenit Heart Surg 2018; 9 (06) 677-684
  • 2 Fontan F, Baudet E. Surgical repair of tricuspid atresia. Thorax 1971; 26 (03) 240-248
  • 3 Vener DF, Gaies M, Jacobs JP, Pasquali SK. Clinical databases and registries in congenital and pediatric cardiac surgery, cardiology, critical care, and anesthesiology worldwide. World J Pediatr Congenit Heart Surg 2017; 8 (01) 77-87
  • 4 Day RW, Denton DM, Jackson WD. Growth of children with a functionally single ventricle following palliation at moderately increased altitude. Cardiol Young 2000; 10 (03) 193-200
  • 5 Cohen MI, Bush DM, Ferry Jr RJ. et al. Somatic growth failure after the Fontan operation. Cardiol Young 2000; 10 (05) 447-457
  • 6 François K, Bové T, Panzer J. et al. Univentricular heart and Fontan staging: analysis of factors impacting on body growth. Eur J Cardiothorac Surg 2012; 41 (06) e139-e145
  • 7 Ovroutski S, Ewert P, Alexi-Meskishvili V. et al. Comparison of somatic development and status of conduit after extracardiac Fontan operation in young and older children. Eur J Cardiothorac Surg 2004; 26 (06) 1073-1079
  • 8 Ono M, Boethig D, Goerler H, Lange M, Westhoff-Bleck M, Breymann T. Somatic development long after the Fontan operation: factors influencing catch-up growth. J Thorac Cardiovasc Surg 2007; 134 (05) 1199-1206
  • 9 Vogt KN, Manlhiot C, Van Arsdell G, Russell JL, Mital S, McCrindle BW. Somatic growth in children with single ventricle physiology impact of physiologic state. J Am Coll Cardiol 2007; 50 (19) 1876-1883
  • 10 Anderson JB, Iyer SB, Schidlow DN. et al; National Pediatric Cardiology Quality Improvement Collaborative. Variation in growth of infants with a single ventricle. J Pediatr 2012; 161 (01) 16-21 .e1, quiz 21.e2–21.e3
  • 11 Williams RV, Zak V, Ravishankar C. et al; Pediatric Heart Network Investigators. Factors affecting growth in infants with single ventricle physiology: a report from the Pediatric Heart Network Infant Single Ventricle Trial. J Pediatr 2011; 159 (06) 1017-22.e2
  • 12 Hessel TW, Greisen G, Idorn L, Reimers JI. Somatic growth in 94 single ventricle children – comparing systemic right and left ventricle patients. Acta Paediatr 2013; 102 (01) 35-39
  • 13 Wellnitz K, Harris IS, Sapru A, Fineman JR, Radman M. Longitudinal development of obesity in the post-Fontan population. Eur J Clin Nutr 2015; 69 (10) 1105-1108
  • 14 Lambert LM, McCrindle BW, Pemberton VL. et al; Pediatric Heart Network Investigators. Longitudinal study of anthropometry in Fontan survivors: pediatric Heart Network Fontan study. Am Heart J 2020; 224: 192-200
  • 15 Van den Eynde J, Bartelse S, Rijnberg FM. et al. Somatic growth in single ventricle patients: a systematic review and meta-analysis. Acta Paediatr 2023; 112 (02) 186-199
  • 16 Granegger M, Küng S, Bollhalder O. et al. Serial assessment of somatic and cardiovascular development in patients with single ventricle undergoing Fontan procedure. Int J Cardiol 2021; 322: 135-141
  • 17 Schreiber C, Hörer J, Vogt M, Cleuziou J, Prodan Z, Lange R. Nonfenestrated extracardiac total cavopulmonary connection in 132 consecutive patients. Ann Thorac Surg 2007; 84 (03) 894-899
  • 18 Ono M, Kasnar-Samprec J, Hager A. et al. Clinical outcome following total cavopulmonary connection: a 20-year single-centre experience. Eur J Cardiothorac Surg 2016; 50 (04) 632-641
  • 19 Stenbøg EV, Hjortdal VE, Ravn HB, Skjaerbaek C, Sørensen KE, Hansen OK. Improvement in growth, and levels of insulin-like growth factor-I in the serum, after cavopulmonary connections. Cardiol Young 2000; 10 (05) 440-446
  • 20 Danilowicz DA. Delay in bone age in children with cyanotic congenital heart disease. Radiology 1973; 108 (03) 655-658
  • 21 Witzel C, Sreeram N, Coburger S, Schickendantz S, Brockmeier K, Schoenau E. Outcome of muscle and bone development in congenital heart disease. Eur J Pediatr 2006; 165 (03) 168-174
  • 22 McCrindle BW, Williams RV, Mital S. et al. Reduced physical activity levels after the Fontan procedure: related to exercise capacity or own health perception?. Arch Dis Child 2007; 92: 509-514
  • 23 Baldini L, Librandi K, D'Eusebio C, Lezo A. Nutritional management of patients with fontan circulation: a potential for improved outcomes from birth to adulthood. Nutrients 2022; 14 (19) 4055