دورية أكاديمية

Hydrops and congenital diaphragmatic hernia: reported incidence and postnatal outcomes. Analysis of the congenital diaphragmatic hernia study group registry.

التفاصيل البيبلوغرافية
العنوان: Hydrops and congenital diaphragmatic hernia: reported incidence and postnatal outcomes. Analysis of the congenital diaphragmatic hernia study group registry.
المؤلفون: Mesas Burgos C; Department of Pediatric Surgery, Karolinska University Hospital and Karolinska Institute, Stockholm, Sweden. carmen.mesas.burgos@ki.se., Ebanks AH; Department of Pediatric Surgery, McGovern Medical School at UT Health and Children's Memorial Hermann Hospital, Houston, TX, USA., Löf-Granström A; Department of Pediatric Surgery, Karolinska University Hospital and Karolinska Institute, Stockholm, Sweden., Holden KI; Department of Pediatric Surgery, McGovern Medical School at UT Health and Children's Memorial Hermann Hospital, Houston, TX, USA., Johnson A; The Fetal Center, Children's Memorial Hermann Hospital, University of Texas Health Science Center, Houston, TX, USA., Conner P; Center for Fetal Medicine, Karolinska University Hospital and Karolinska Institute, Stockholm, Sweden., Harting MT; Department of Pediatric Surgery, McGovern Medical School at UT Health and Children's Memorial Hermann Hospital, Houston, TX, USA.
مؤلفون مشاركون: Congenital Diaphragmatic Hernia Study Group
المصدر: Journal of perinatology : official journal of the California Perinatal Association [J Perinatol] 2024 May 30. Date of Electronic Publication: 2024 May 30.
Publication Model: Ahead of Print
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: United States NLM ID: 8501884 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5543 (Electronic) Linking ISSN: 07438346 NLM ISO Abbreviation: J Perinatol Subsets: MEDLINE
أسماء مطبوعة: Publication: 2001- : New York, NY : Nature Publishing Group
Original Publication: [Philadelphia, Pa. : W.B. Saunders, c1984-
مستخلص: Objective: Congenital Diaphragmatic Hernia (CDH) associated with hydrops is rare. The aim of this study was to describe the incidence of this combination of anomalies and the postnatal outcomes from a large database for CDH.
Study Design: Data from the multicenter, multinational database on infants with prenatally diagnosed CDH (CDHSG Registry) born from 2015 to 2021 were analyzed.
Results: A total of 3985 patients were entered in the registry during the study period, 3156 were prenatally diagnosed and 88 were reported to have associated fluid in at least 1 compartment, representing 2.8% of all prenatally diagnosed CDH cases in the registry. The overall survival to discharge for CDH patients with hydrops was 43%. The hydropic CDH group had lower birth weight and gestational age at birth, and increased incidence of right-sided CDH (55%), and rate of non-repair (45%). However, the survival rate for hydropic infants with CDH undergoing surgical repair was 80%. Other associated anomalies were more common in hydropic CDH (50% vs 37%, p = 0.001).
Conclusion: Hydropic CDH is rare, only 2.8% of all prenatally diagnosed cases, and more commonly occurring in right-sided CDH. Survival rates are low, with higher rates of non-repair. However, decision-making regarding goals of care and an aggressive surgical approach in selected cases may result in survival rates comparable to non-hydropic cases.
(© 2024. The Author(s).)
References: Burgos CM, Frenckner B. Addressing the hidden mortality in CDH: a population-based study. J Pediatr Surg. 2017;52:522–5. (PMID: 10.1016/j.jpedsurg.2016.09.06127745705)
Lally P. Report from the Congenital Diaphragmatic Hernia Study Group Database. CDHSG. 2008. http://cdhsg.net/ .
Mesas Burgos C, Hammarqvist-Vejde J, Frenckner B, Conner P. Differences in outcomes in prenatally diagnosed congenital diaphragmatic hernia compared to postnatal detection: a single-center experience. Fetal diagnosis and therapy 2016;39:241–7.
Burgos CM, Frenckner B, Luco M, Harting MT, Lally PA, Lally KP, et al. Prenatally versus postnatally diagnosed congenital diaphragmatic hernia - side, stage, and outcome. J Pediatr Surg. 2019;54:651–5.
Monier I, Lelong N, Benachi A, Jouannic JM, Khoshnood B, Zeitlin J. Postnatal diagnosis of congenital anomalies despite active systematic prenatal screening policies: a population-based registry study. Am J Obstet Gynecol MFM. 2023;5:101170. (PMID: 10.1016/j.ajogmf.2023.10117037783275)
Haroon J, Chamberlain RS. An evidence-based review of the current treatment of congenital diaphragmatic hernia. Clin Pediatr (Philos). 2013;52:115–24. (PMID: 10.1177/0009922812472249)
Danzer E, Hedrick HL. Controversies in the management of severe congenital diaphragmatic hernia. Semin Fetal Neonatal Med. 2014;19:376–84. (PMID: 10.1016/j.siny.2014.10.00125454678)
Akinkuotu AC, Cruz SM, Abbas PI, Lee TC, Welty SE, Olutoye OO, et al. Risk-stratification of severity for infants with CDH: prenatal versus postnatal predictors of outcome. J Pediatr Surg. 2016;51:44–8. (PMID: 10.1016/j.jpedsurg.2015.10.00926563530)
Jani J, Keller RL, Benachi A, Nicolaides KH, Favre R, Gratacos E, et al. Prenatal prediction of survival in isolated left-sided diaphragmatic hernia. Ultrasound Obstet Gynecol. 2006;27:18–22. (PMID: 10.1002/uog.268816374756)
Hedrick HL, Danzer E, Merchant A, Bebbington MW, Zhao H, Flake AW, et al. Liver position and lung-to-head ratio for prediction of extracorporeal membrane oxygenation and survival in isolated left congenital diaphragmatic hernia. Am J Obstet Gynecol. 2007;197:422.e1–4. (PMID: 10.1016/j.ajog.2007.07.00117904987)
Cannie M, Jani J, Meersschaert J, Allegaert K, Done E, Marchal G, et al. Prenatal prediction of survival in isolated diaphragmatic hernia using observed to expected total fetal lung volume determined by magnetic resonance imaging based on either gestational age or fetal body volume. Ultrasound Obstet Gynecol. 2008;32:633–9. (PMID: 10.1002/uog.613918792417)
Gucciardo L, Deprest J, Done E, Van Mieghem T, Van de Velde M, Gratacos E, et al. Prediction of outcome in isolated congenital diaphragmatic hernia and its consequences for fetal therapy. Best Pract Res Clin Obstet Gynaecol. 2008;22:123–38. (PMID: 10.1016/j.bpobgyn.2007.08.00618082455)
Jani JC, Benachi A, Nicolaides KH, Allegaert K, Gratacos E, Mazkereth R, et al. Prenatal prediction of neonatal morbidity in survivors with congenital diaphragmatic hernia: a multicenter study. Ultrasound Obstet Gynecol. 2009;33:64–9. (PMID: 10.1002/uog.614118844275)
Cordier AG, Jani JC, Cannie MM, Rodo C, Fabietti I, Persico N, et al. Stomach position in the prediction of survival in left-sided congenital diaphragmatic hernia with or without fetoscopic endoluminal tracheal occlusion. Ultrasound Obstet Gynecol. 2015;28:190–5.
Lee JY, Jun JK, Lee J. Prenatal prediction of neonatal survival in cases diagnosed with congenital diaphragmatic hernia using abdomen-to-thorax ratio determined by ultrasonography. J Obstet Gynaecol Res. 2014;40:2037–43. (PMID: 10.1111/jog.1247325181624)
Neveling S, Knippel AJ, Kozlowski P. Isolated non-immune hydrops fetalis: an observational study on complete spontaneous resolution, perinatal outcome, and long-term follow-up. Arch Gynecol Obstet. 2023;308:487–97. (PMID: 10.1007/s00404-022-06731-w35994111)
Vanaparthy R, Mahdy H. Hydrops fetalis. Treasure Island (FL): StatPearls; 2023.
Wei X, Yang Y, Zhou J, Zhou X, Xiong S, Chen J, et al. An investigation of the etiologies of non-immune hydrops fetalis in the era of next-generation sequence-a single center experience. Genes. 2022;13:2231. (PMID: 10.3390/genes13122231365534979778190)
Ibrahim M, Hunter M, Gugasyan L, Chan Y, Malhotra A, Sehgal A, et al. Interstitial deletion of chromosome 1 (1p21.1p12) in an infant with congenital diaphragmatic hernia, hydrops fetalis, and interrupted aortic arch. Clin Case Rep. 2017;5:164–9. (PMID: 10.1002/ccr3.759281746445290521)
Rossi A, Delabaere A, Delmas-Laurichesse H, Beaufrere AM, Lemery D, Gallot D. The challenge of prenatal identification of congenital diaphragmatic hernia in the context of hydrops. Eur J Obstet Gynecol Reprod Biol. 2014;182:238–9. (PMID: 10.1016/j.ejogrb.2014.09.04225445106)
Sydorak RM, Goldstein R, Hirose S, Tsao K, Farmer DL, Lee H, et al. Congenital diaphragmatic hernia and hydrops: a lethal association? J Pediatr Surg. 2002;37:1678–80. (PMID: 10.1053/jpsu.2002.3669112483628)
Lally KP, Lasky RE, Lally PA, Bagolan P, Davis CF, Frenckner BP, et al. Standardized reporting for congenital diaphragmatic hernia-an international consensus. J Pediatr Surg. 2013;48:2408–15. (PMID: 10.1016/j.jpedsurg.2013.08.01424314179)
Giacoia GP. Right-sided diaphragmatic hernia associated with superior vena cava syndrome. Am J Perinatol. 1994;11:129–31. (PMID: 10.1055/s-2007-9945728198654)
Tolia VN, Hunter Clark R Jr, Perelmuter B, Frankfurt JA, Ahmad KA, Abrams ME, et al. Hydrops fetalis-trends in associated diagnoses and mortality from 1997-2018. J Perinatol. 2021;41:2537–43. (PMID: 10.1038/s41372-021-01179-334385586)
Bullard KM, Harrison MR. Before the horse is out of the barn: fetal surgery for hydrops. Semin Perinatol. 1995;19:462–73. (PMID: 10.1016/S0146-0005(05)80053-98822330)
Asmal M, Suri M, Ruzal-Shapiro CB, Baxi LV. Non-immune hydrops and superior vena cava syndrome due to diaphragmatic hernia in one twin. Fetal Diagn Ther. 2004;19:377–80. (PMID: 10.1159/00007797015192301)
Benacerraf BR, Frigoletto FD Jr. In utero treatment of a fetus with diaphragmatic hernia complicated by hydrops. Am J Obstet Gynecol. 1986;155:817–8. (PMID: 10.1016/S0002-9378(86)80027-83532803)
Sperling JD, Sparks TN, Berger VK, Farrell JA, Gosnell K, Keller RL, et al. Prenatal diagnosis of congenital diaphragmatic hernia: does laterality predict perinatal outcomes? Am J Perinatol. 2018;35:919–24. (PMID: 10.1055/s-0037-1617754293045456033692)
Mesas Burgos C, Frenckner B, Luco M, Harttig M, Lally P, Lally K. Right versus left congenital diaphragmatic hernia – what’s the difference? J Pediatr Surg. 2017. https://doi.org/10.1016/j.jpedsurg.2017.10.027 .
Kimura O, Furukawa T, Higuchi K, Takeuchi Y, Fumino S, Aoi S, et al. Impact of our new protocol on the outcome of the neonates with congenital diaphragmatic hernia. Pediatr Surg Int. 2013;29:335–9. (PMID: 10.1007/s00383-012-3242-z23292533)
Rocha G, Baptista MJ, Correia-Pinto J, Guimaraes H. Congenital diaphragmatic hernia: experience of 14 years. Minerva Pediatr. 2013;65:271–8. (PMID: 23685378)
تواريخ الأحداث: Date Created: 20240530 Latest Revision: 20240530
رمز التحديث: 20240531
DOI: 10.1038/s41372-024-02010-5
PMID: 38816581
قاعدة البيانات: MEDLINE
الوصف
تدمد:1476-5543
DOI:10.1038/s41372-024-02010-5