Pulmonary function in children and adolescents after esophageal atresia repair

Felipe Donoso, Hans Hedenström, Andrei Malinovschi, Helene E Lilja, Felipe Donoso, Hans Hedenström, Andrei Malinovschi, Helene E Lilja

Abstract

Introduction: Respiratory morbidity after esophageal atresia (EA) is common. The aims of this study were to assess pulmonary function, to identify risk factors for pulmonary function impairment (PFI), and to investigate the relations between respiratory morbidity, defined as medical treatment for respiratory symptoms or recent pneumonia and PFI after EA repair.

Material and methods: Single center retrospective observational study including patients with EA who participated in the follow-up program for 8- or 15-year old patients from 2014 to 2018 and performed pulmonary function testing by body plethysmography, dynamic spirometry, impulse oscillometry, and diffusing capacity of the lungs. Univariate and multiple stepwise logistic regression with PFI as outcome were performed. Anastomotic leak, episodes of general anesthesia, extubation day, birth weight, age at follow up, gross classification, and abnormal reflux index were independent variables.

Results: In total, 47 patients were included. PFI was found in 19 patients (41%) and 16 out of 19 patients (84%) had an obstructive pattern. Respiratory morbidity was found in 23 (52%, NA = 3) of the patients with no correlation to PFI. Birth weight, age at follow-up, and episodes of general anesthesia were identified as risk factors for PFI.

Conclusion: Respiratory morbidity and PFI were common in children and adolescents after EA repair. The major component of PFI was obstruction of the airways. The risk for PFI increased with lower birth weight and older age at follow up. The poor correlation between respiratory morbidity and PFI motivates the need of clinical follow up including pulmonary function tests.

Keywords: esophageal atresia; pulmonary function; respiratory morbidity.

© 2019 The Authors. Pediatric Pulmonology published by Wiley Periodicals, Inc.

References

    1. Oddsberg J, Lu Y, Lagergren J. Aspects of esophageal atresia in a population‐based setting: incidence, mortality, and cancer risk. Pediatr Surg Int. 2012;28(3):249‐257. 10.1007/s00383-011-3014-1
    1. Gatzinsky V, Jönsson L, Johansson C, Göthberg G, Sillén U, Friberg LG. Dysphagia in adults operated on for esophageal atresia—use of a symptom score to evaluate correlated factors. Eur J Pediatr Surg. 2011;21(2):94‐98. 10.1055/s-0030-1270454
    1. Sistonen SJ, Pakarinen MP, Rintala RJ. Long‐term results of esophageal atresia: Helsinki experience and review of literature. Pediatr Surg Int. 2011;27(11):1141‐1149. 10.1007/s00383-011-2980-7
    1. Legrand C, Michaud L, Salleron J, et al. Long‐term outcome of children with oesophageal atresia type III. Arch Dis Child. 2012;97(9):808‐811. 10.1136/archdischild-2012-301730
    1. Peetsold M, Heij H, Deurloo J, Gemke R. Health‐related quality of life and its determinants in children and adolescents born with oesophageal atresia. Acta Paediatr Int J Paediatr. 2010;99(3):411‐417. 10.1111/j.1651-2227.2009.01579.x
    1. Koivusalo A, Pakarinen MP, Turunen P, Saarikoski H, Lindahl H, Rintala RJ. Health‐related quality of life in adult patients with esophageal atresia—a questionnaire study. J Pediatr Surg. 2005;40(2):307‐312. 10.1016/j.jpedsurg.2004.10.014
    1. Gischler SJ, van der Cammen‐van Zijp MHM, Mazer P, et al. A prospective comparative evaluation of persistent respiratory morbidity in esophageal atresia and congenital diaphragmatic hernia survivors. J Pediatr Surg. 2009;44(9):1683‐1690. 10.1016/j.jpedsurg.2008.12.019
    1. Sistonen S, Malmberg P, Malmstrom K, et al. Repaired oesophageal atresia: respiratory morbidity and pulmonary function in adults. Eur Respir J. 2010;36(5):1106‐1112. 10.1183/09031936.00153209
    1. Gallo G, Vrijlandt EJLE, Arets HGM, et al. Respiratory function after esophageal replacement in children. J Pediatr Surg. 2017;52(11):1736‐1741. 10.1016/j.jpedsurg.2017.03.046
    1. Chetcuti P, Phelan PD, Greenwood R. Lung function abnormalities in repaired oesophageal atresia and tracheo‐oesophageal fistula. Thorax. 1992;47:1030‐1034.
    1. Malmström K, Lohi J, Lindahl H, et al. Longitudinal follow‐up of bronchial inflammation, respiratory symptoms, and pulmonary function in adolescents after repair of esophageal atresia with tracheoesophageal fistula. J Pediatr. 2008;153(3):396‐401.e1. 10.1016/j.jpeds.2008.03.034
    1. Kovesi T, Rubin S. Long‐term complications of congenital esophageal atresia and/or tracheoesophageal fistula. Chest. 2004;126(3):915‐925. 10.1378/chest.126.3.915
    1. Quanjer PH, Stanojevic S, Cole TJ, et al. Multi‐ethnic reference values for spirometry for the 3‐95‐yr age range: the global lung function 2012 equations. Eur Respir J. 2012;40(6):1324‐1343. 10.1183/09031936.00080312
    1. Nowowiejska B, Tomalak W, Radliński J, Siergiejko G, Latawiec W, Kaczmarski M. Transient reference values for impulse oscillometry for children aged 3‐18 years. Pediatr Pulmonol. 2008;43(12):1193‐1197. 10.1002/ppul.20926
    1. Stanojevic S, Graham BL, Cooper BG, et al. Official ERS technical standards: global lung function initiative reference values for the carbon monoxide transfer factor for Caucasians. Eur Respir J. 2017;50(3):1700010 10.1183/13993003.00010-2017
    1. Harrison J, Martin J, Crameri J, Robertson CF, Ranganathan SC. Lung function in children with repaired tracheo‐oesophageal fistula using the forced oscillation technique. Pediatr Pulmonol. 2010;45(11):1057‐1063. 10.1002/ppul.21282
    1. Peetsold MG, Heij HA, Nagelkerke AF, Deurloo JA, Gemke RJBJ. Pulmonary function impairment after trachea‐esophageal fistula: a minor role for gastro‐esophageal reflux disease. Pediatr Pulmonol. 2011;46(4):348‐355. 10.1002/ppul.21369
    1. Pedersen RN, Markøw S, Kruse‐Andersen S, et al. Long‐term pulmonary function in esophageal atresia—a case‐control study. Pediatr Pulmonol. 2017;52(1):98‐106. 10.1002/ppul.23477
    1. Dittrich R, Stock P, Rothe K, Degenhardt P. Pulmonary outcome of esophageal atresia patients and its potential causes in early childhood. J Pediatr Surg. 2017;52(8):1255‐1259. 10.1016/j.jpedsurg.2016.12.025
    1. Beucher J, Wagnon J, Daniel V, et al. Long‐term evaluation of respiratory status after esophageal atresia repair. Pediatr Pulmonol. 2013;48(2):188‐194. 10.1002/ppul.22582
    1. Toussaint‐Duyster LCC, Van der cammen‐Van zijp MHM, Spoel M, et al. Determinants of exercise capacity in school‐aged esophageal atresia patients. Pediatr Pulmonol. 2017;52:1198‐1205. 10.1002/ppul.23687 September 2016
    1. Pellegrino R, Viegi G., Brusasco V., et al. Interpretative strategies for lung function tests. Eur Respir J. 2005;26(5):948‐968. 10.1183/09031936.05.00035205
    1. Solymar L, Aronsson PH, Bake B, Bjure J. Nitrogen single breath test, flow‐volume curves and spirometry in healthy children, 7‐18 years of age. Eur J Respir Dis. 1980;61(5):275‐286.
    1. Polgar G, Promadhat V. Pulmonary Function Testing in Children: Techniques and Standards Philadelphia (Pa.): Saunders; 1971.
    1. Quanjer PH, Borsboom GJ, Brunekreef B, et al. Spirometric reference values for white European children and adolescents: Polgar revisited. Pediatr Pulmonol. 1995;19:135‐142.
    1. Mercedes de Onis, Cutberto Garza, Onyango RM Adelheid W. The WHO child growth standards. Acta Pædiatrica Int J Pædiatrics. 2006;95(suppl 450):1‐104.
    1. WHO Multicentre Growth Reference Study Group . WHO Child Growth Standards: Length/height‐for‐age, weight‐for‐age, weight‐for‐length, weight‐for‐height and body mass index‐for‐age: Methods and development Geneva: World Health Organization; 2006.
    1. de Onis M. Development of a WHO growth reference for school‐aged children and adolescents. Bull World Health Organ. 2007;85:660‐667. 10.2471/BLT07.043497 September 2007.
    1. Rodd C, Metzger DL, Sharma A. Extending World Health Organization weight‐for‐age reference curves to older children. BMC Pediatr. 2014;14(1):1‐7. 10.1186/1471-2431-14-32
    1. CPEG. Calculator: WHO anthropometric Z‐scores 0‐19y.
    1. Olbers J, Gatzinsky V, Jönsson L, et al. Physiological studies at 7 years of age in children born with esophageal atresia. Eur J Pediatr Surg. 2015;25(5):397‐404. 10.1055/s-0034-1390017
    1. Kovesi T. Long‐term respiratory complications of congenital esophageal atresia with or without tracheoesophageal fistula: an update. Dis Esophagus. 2013;26(4):413‐416. 10.1111/dote.12061
    1. Komarow HD, Myles IA, Uzzaman A, Metcalfe DD. Impulse oscillometry in the evaluation of diseases of the airways in children. Ann Allergy Asthma Immunol. 2011;106(3):191‐199. 10.1016/j.anai.2010.11.011
    1. Sørensen JK, Buchvald F, Berg AK, Robinson PD, Nielsen KG. Ventilation inhomogeneity and NO and CO diffusing capacity in ex‐premature school children. Respir Med. 2018;140:94‐100. 10.1016/j.rmed.2018.06.006
    1. Doyle LW, Adams AM, Robertson C, et al. Increasing airway obstruction from 8 to 18 years in extremely preterm/low‐birthweight survivors born in the surfactant era. Thorax. 2017;72(8):712‐719. 10.1136/thoraxjnl-2016-208524
    1. Lilja HE, Wester T. Outcome in neonates with esophageal atresia treated over the last 20 years. Pediatr Surg Int. 2008;24(5):531‐536. 10.1007/s00383-008-2122-z
    1. Gatzinsky V, Jönsson L, Ekerljung L, Friberg L‐G, Wennergren G. Long‐term respiratory symptoms following oesophageal atresia. Acta Paediatr. 2011;100(9):1222‐1225. 10.1111/j.1651-2227.2011.02279.x
    1. Koivusalo AI, Pakarinen MP, Rintala RJ. Modern outcomes of oesophageal atresia: single centre experience over the last twenty years. J Pediatr Surg. 2013;48(2):297‐303. 10.1016/j.jpedsurg.2012.11.007
    1. Pini Prato A, Carlucci M, Bagolan P, et al. A cross‐sectional nationwide survey on esophageal atresia and tracheoesophageal fistula. J Pediatr Surg. 2015;50(9):1441‐1456. 10.1016/j.jpedsurg.2015.01.004

Source: PubMed

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