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DOI: 10.1055/a-2631-4152
Postnatal Outcomes and Surgical Implications of Somatex™ Thoracoamniotic Shunting for CPAM: A Multicenter Experience
Funding None.

Abstract
Introduction
Intrauterine thoracoamniotic shunting in fetuses with congenital pulmonary airway malformation (CPAM) was first described using Cook™ or Rocket™ shunts. With the availability of the Somatex™ intrauterine shunt, a new device with the supposed advantages of less invasive placement and less frequent dislocations, pediatric surgeons and neonatologists are increasingly confronted with a new cohort of patients. Data on postnatal findings and the impact on surgical management are scarce.
Materials and Methods
We conducted a multicenter retrospective study of all children born after prenatal treatment with a Somatex™ thoracoamniotic shunt for suspected CPAM. We analyzed the clinical and respiratory conditions of the children at birth as well as shunt locations, removal procedures, and timing of surgery.
Results
Twelve patients were included. 8/12 patients presented postnatally with pneumothorax, necessitating in all cases the placement of a chest tube. In 6/12 patients, the removal of the Somatex™ shunt had to be done surgically, bedside removal was possible in 5 patients. One patient was born without the shunt due to intrauterine dislocation. All patients were operated on using a muscle-sparing thoracotomy, at ages ranging from 1 to 42 days; only one could be discharged before surgery. One patient underwent emergency surgery. With a median follow-up of 19 months, 11/12 patients survived.
Conclusion
Despite the small number of patients and the retrospective aspect of this study, our observations showed that intrauterine treatment of CPAM with the Somatex™ shunt is frequently associated with postnatal complications. Neonatologists and pediatric surgeons must be aware of the high rate of pneumothorax and the presumable necessity of early surgical intervention.
Clinical Trial Registration
None.
Publication History
Received: 05 March 2025
Accepted: 07 June 2025
Article published online:
23 June 2025
© 2025. Thieme. All rights reserved.
Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany
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References
- 1 Pederiva F, Rothenberg SS, Hall N. et al. Congenital lung malformations. Nat Rev Dis Primers 2023; 9 (01) 60
- 2 Muntean A, Cazacu R, Ade-Ajayi N, Patel SB, Nicolaides K, Davenport M. The long-term outcome following thoraco-amniotic shunting for congenital lung malformations. J Pediatr Surg 2023; 58 (02) 213-217
- 3 Jeong BD, Won HS, Lee MY, Shim JY, Lee PR, Kim A. Perinatal outcomes of fetal pleural effusion following thoracoamniotic shunting. Prenat Diagn 2015; 35 (13) 1365-1370
- 4 Wada S, Jwa SC, Yumoto Y. et al. The prognostic factors and outcomes of primary fetal hydrothorax with the effects of fetal intervention. Prenat Diagn 2017; 37 (02) 184-192
- 5 Morini F, Zani A, Conforti A. et al. Current management of congenital pulmonary airway malformations: A “European Pediatric Surgeons' Association” survey. Eur J Pediatr Surg 2018; 28 (01) 1-5
- 6 Weber M, Monier I, Rahshenas M. et al.; MALFPULM Study Group. Fetal therapy for congenital pulmonary malformations: A prospective population-based national cohort study. Prenat Diagn 2024; 44 (12) 1536-1547
- 7 Abbasi N, Windrim R, Keunen J. et al. Perinatal outcome in fetuses with dislodged thoraco-amniotic shunts. Fetal Diagn Ther 2021; 48 (06) 430-439
- 8 Rosenblat O, Furman Y, Kimhi G. et al. In-utero treatment of prenatal thoracic abnormalities by thoraco-amniotic shunts, short and long term neuro developmental outcome: A single center experience. J Pediatr Surg 2022; 57 (03) 364-368
- 9 Macchini F, Mazzoleni S, Cavallaro G, Persico N, Borzani I, Leva E. Combined pre- and postnatal minimally invasive approach to a complex symptomatic congenital pulmonary airway malformation. European J Pediatr Surg Rep 2023; 11 (01) e36-e39
- 10 Grandt J, Gottschalk I, Geipel A. et al. Intrauterine Thoracoamniotic shunting of fetal hydrothorax with the somatex intrauterine shunt: intrauterine course and postnatal outcome. J Clin Med 2022; 11 (09) 2312
- 11 Woodward JM, Mendel R, Brierley SF. et al. Operative timing for elective thoracoscopic lobectomy for CPAM and sequestration: A NSQIP-Pediatric Analysis 2017-2021. J Pediatr Surg 2024; 59 (12) 161681
- 12 Esposito C, Bonnard A, Till H. et al. Thoracoscopic management of pediatric patients with congenital lung malformations: Results of a European multicenter survey. J Laparoendosc Adv Surg Tech A 2021; 31 (03) 355-362
- 13 König TT, Frankenbach ML, Gianicolo E. et al. Habitual physical activity in patients born with oesophageal atresia: a multicenter cross-sectional study and comparison to a healthy reference cohort matched for gender and age. Eur J Pediatr 2023; 182 (06) 2655-2663
- 14 Kohaut J, Holtkamp G, Fischer-Mertens J. et al. A new spectrum of neonatal urethral pathologies in the era of early vesicoamniotic shunting?. World J Urol 2024; 42 (01) 589
- 15 Kohaut J, Fischer-Mertens J, Cernaianu G. et al. Postnatal surgical treatment and complications following intrauterine vesicoamniotic shunting with the SOMATEX® intrauterine shunt. A single center experience. J Pediatr Urol 2023; 19 (05) 567.e1-567.e6
- 16 Muntean A, Marsland L, Sikdar O. et al. Neonatal surgery for congenital lung malformations: Indications, outcomes and association with malignancy. J Pediatr Surg 2025; 60 (05) 162253
- 17 Dalton SE, Griffith AM, Kennedy AM, Woodward PJ. Differential diagnosis of hydrops fetalis: An imaging guide. Radiographics 2025; 45 (03) e240158