CC BY-NC-ND 4.0 · Journal of Fetal Medicine
DOI: 10.1055/s-0044-1786166
Case Report

Ultrasound Differentiation of Twins with Discordant Congenital Diaphragmatic Hernia in the Delivery Room

1   Department of Pediatrics, Division of Neonatology, New York-Presbyterian/Weill Cornell Medical Center, New York, New York, United States
,
Ericalyn Kasdorf
1   Department of Pediatrics, Division of Neonatology, New York-Presbyterian/Weill Cornell Medical Center, New York, New York, United States
,
Sara Cohen
2   Department of Radiology, Division of Pediatric Radiology, New York-Presbyterian/Weill Cornell Medical Center, New York, New York, United States
,
Arzu Kovanlikaya
2   Department of Radiology, Division of Pediatric Radiology, New York-Presbyterian/Weill Cornell Medical Center, New York, New York, United States
,
Brittany Roser
3   Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine, New York-Presbyterian/Weill Cornell Medical Center, New York, New York, United States
,
Corrina Oxford-Horrey
3   Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine, New York-Presbyterian/Weill Cornell Medical Center, New York, New York, United States
,
Cynthia Perez
1   Department of Pediatrics, Division of Neonatology, New York-Presbyterian/Weill Cornell Medical Center, New York, New York, United States
,
Catherine Chang
4   Department of Pediatrics, Division of Neonatology, University of Utah Health, Salt Lake City, Utah, United States
› Author Affiliations
Funding None.

Abstract

Most infants with prenatally diagnosed congenital diaphragmatic hernia (CDH) are intubated rapidly after birth to optimize oxygenation and ventilation while avoiding abdominal distention and high mean airway pressures. A twin pregnancy complicated by one twin with a CDH diagnosis is a rare event and is associated with preterm delivery and low birth weight compared to singletons with CDH. In rare cases of discordant CDH in twin pregnancies with an absence of external distinguishing features (similar weights, fetal presentation, and sex), it may be difficult to quickly determine which twin has CDH in the delivery room (DR), raising ambiguity about the best management of both infants. This case describes the successful use of ultrasound (US) in the DR to rapidly diagnose the presence or absence of CDH in discordant twins. By developing a resuscitation algorithm and using in situ simulations prior to delivery, the twin with CDH was rapidly identified, intubated, and transported to the neonatal intensive care unit (NICU) for further management. The twin without CDH received routine care and was transferred to the well-baby nursery. Interprofessional planning and simulation may be used to design a safe resuscitation plan incorporating US diagnosis of diaphragmatic anomalies into the Neonatal Resuscitation Program (NRP) algorithm.

Author Contributions

S.M.C wrote the first draft of the manuscript with specific contributions from B.R. and S.H.S.M.C, E.K., C.P., C.C., S.C., A.K., B.R., and C.O.-H. contributed to the conception and design of the study, critical revision of the manuscript for important intellectual input, gave final approval of the manuscript, and agree to be accountable for all aspects of the work.


Study Approval Statement

This study protocol was reviewed and approved by Weill Cornell Medicine Institutional Review Board (approval number: 21-12024204).


Patients' Consent

The parents of these children provided written informed consent for publication of this case report and use of the images therein.




Publication History

Article published online:
19 April 2024

© 2024. Society of Fetal Medicine. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • References

  • 1 Horn-Oudshoorn EJJ, Knol R, Te Pas AB. et al. Perinatal stabilisation of infants born with congenital diaphragmatic hernia: a review of current concepts. Arch Dis Child Fetal Neonatal Ed 2020; 105 (04) 449-454
  • 2 Puligandla PS, Skarsgard ED, Offringa M. et al; Canadian Congenital Diaphragmatic Hernia Collaborative. Diagnosis and management of congenital diaphragmatic hernia: a clinical practice guideline. CMAJ 2018; 190 (04) E103-E112
  • 3 Jancelewicz T, Brindle ME, Guner YS, Lally PA, Lally KP, Harting MT. Congenital Diaphragmatic Hernia Study Group (CDHSG), Pediatric Surgery Research Collaborative (PedSRC). Toward standardized management of congenital diaphragmatic hernia: an analysis of practice guidelines. J Surg Res 2019; 243: 229-235
  • 4 Reiss I, Schaible T, van den Hout L. et al; CDH EURO Consortium. Standardized postnatal management of infants with congenital diaphragmatic hernia in Europe: the CDH EURO Consortium consensus. Neonatology 2010; 98 (04) 354-364
  • 5 Wyckoff MH, Aziz K, Escobedo MB. et al. Part 13: Neonatal Resuscitation: 2015 American Heart Association Guidelines Update for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation 2015; 132 (18, Suppl 2): S543-S560
  • 6 Abman SH, Hansmann G, Archer SL. et al; American Heart Association Council on Cardiopulmonary, Critical Care, Perioperative and Resuscitation; Council on Clinical Cardiology; Council on Cardiovascular Disease in the Young; Council on Cardiovascular Radiology and Intervention; Council on Cardiovascular Surgery and Anesthesia; and the American Thoracic Society. Pediatric pulmonary hypertension: guidelines from the American Heart Association and American Thoracic Society. Circulation 2015; 132 (21) 2037-2099
  • 7 David TJ, Illingworth CA. Diaphragmatic hernia in the south-west of England. J Med Genet 1976; 13 (04) 253-262
  • 8 Pober BR, Lin A, Russell M. et al. Infants with Bochdalek diaphragmatic hernia: sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program. Am J Med Genet A 2005; 138A (02) 81-88
  • 9 Robert E, Källén B, Harris J. The epidemiology of diaphragmatic hernia. Eur J Epidemiol 1997; 13 (06) 665-673
  • 10 Wang W, Pan W, Chen J, Xie W, Liu M, Wang J. Outcomes of congenital diaphragmatic hernia in one of the twins. Am J Perinatol 2019; 36 (12) 1304-1309
  • 11 Chasen ST, Spiro SJ, Kalish RB, Chervenak FA. Changes in fetal presentation in twin pregnancies. J Matern Fetal Neonatal Med 2005; 17 (01) 45-48
  • 12 Chasen ST, Al-Kouatly HB, Chervenak FA. Correlation between prenatal and neonatal birth order in twin pregnancy. Am J Perinatol 2001; 18 (03) 151-154
  • 13 Keller RL, Glidden DV, Paek BW. et al. The lung-to-head ratio and fetoscopic temporary tracheal occlusion: prediction of survival in severe left congenital diaphragmatic hernia. Ultrasound Obstet Gynecol 2003; 21 (03) 244-249
  • 14 Yamada NK, Fuerch JH, Halamek LP. Modification of the neonatal resuscitation program algorithm for resuscitation of conjoined twins. Am J Perinatol 2016; 33 (04) 420-424
  • 15 Yamada NK, Fuerch JH, Halamek LP. Simulation-based patient-specific multidisciplinary team training in preparation for the resuscitation and stabilization of conjoined twins. Am J Perinatol 2017; 34 (06) 621-626