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DOI: 10.1055/a-1392-1460
Therapie und Outcome von Neugeborenen mit kongenitaler Zwerchfellhernie und angeborenen Herzfehlern
Therapy and Outcome of Neonates with Congenital Diaphragmatic Hernia and Congenital Heart DefectsZusammenfassung
Die Mortalität von Patienten mit isoliert auftretenden angeborenen Zwerchfellhernien liegt in spezialisierten Zentren bei 20–40%. Wesentliche, das Outcome beeinflussende Faktoren, sind die bestehende Lungenhypoplasie, eine daraus resultierende pulmonale Hypertonie, sowie das Vorliegen weiterer Fehlbildungen. Begleitfehlbildungen wie angeborene Herzfehler treten bei ca. 18% aller Neonaten mit Zwerchfellhernie auf. Schwere angeborene Herzfehler wie das hypoplastische Linksherz Syndrom zeigen sich in ca. 8% der Fälle. In einer retrospektiven Analyse des Patientenkollektivs unserer Klinik zwischen 01/2012 und 12/2018 wurde das prä- und postnatale Management, sowie das Outcome von Neugeborenen mit der Kombination aus angeborenen Herzfehlern und Zwerchfellhernien untersucht. Im Studienzeitraum wurden in unserer Klinik 156 Neugeborene mit Zwerchfellhernie behandelt. Bei 10 Patienten (6,4%) lag zusätzlich ein schwerer, bei 11 Patienten (7,1%) ein moderater Herzfehler vor. 6/21 Patienten verstarben im Verlauf des Krankenhausaufenthaltes, davon 3 am ersten Lebenstag. Es zeigte sich eine deutlich geringere Mortalität bei Patienten mit Zwerchfellhernie und moderatem Herzfehler im Vergleich zu schwerem Herzfehler (9 vs. 50%). Besonders hoch lag die Mortalität bei Kindern mit einem univentrikulären Herzen. Trotz einer deutlich reduzierten Prognose bei der Kombination aus angeborenem Herzfehler und Zwerchfellhernie muss nicht generell mit einer infausten Prognose gerechnet werden. In spezialisierten Zentren kann ein kurativer Ansatz erfolgen.
Abstract
The mortality of patients with isolated congenital diaphragmatic hernia (CDH) in specialized centers is 20–40%. The main factors influencing the outcome are the underlying pulmonary hypoplasia, the resulting pulmonary hypertension and the presence of other malformations. Concomitant malformations such as congenital heart defects occur in around 18% of all neonates with a diaphragmatic hernia. Serious congenital heart defects such as hypoplastic left heart syndrome occur in approximately 8% of cases. In a retrospective analysis of the patient collective of our hospital between 01/2012 and 12/2018, the prenatal and postnatal management as well as the outcome of newborns with a combination of congenital heart defects and diaphragmatic hernias were examined. During the study period, 156 newborns with diaphragmatic hernias were treated at our institution. In 10 patients (6.4%) there was also a severe, and in 11 patients (7.1%) a moderate heart defect. 6/21 patients died during their hospital stay, 3 of them on the first day of life. There was a significantly lower mortality in patients with diaphragmatic hernia and moderate heart defects compared to severe heart defects (9 vs. 50%). The mortality in children with a univentricular heart was particularly high. Despite a significantly reduced prognosis for the combination of congenital heart defects and diaphragmatic hernia, generally a poor prognosis does not have to be expected. A curative approach can be achieved in specialized centers.
Schlüsselwörter
Kongenitale Zwerchfellhernie - Angeborener Herzfehler - Pulmonale Hypertonie - Lungenhypoplasie - extrakorporale Membranoxygenierung (ECMO)Key words
Congenital diaphragmatic hernia - congenital heart defect - pulmonary hypertension - lung hypoplasia - extracorporeal membrane oxygenation (ECMO)Publication History
Received: 05 November 2020
Accepted after revision: 09 February 2021
Article published online:
10 March 2021
© 2021. Thieme. All rights reserved.
Georg Thieme Verlag KG
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Literaturverzeichnis
- 1 Granjo Morais C, Rocha G, Flor-de-Lima F. et al. Predictors of prognosis in neonates with congenital diaphragmatic hernia: experience of 12 years. J Pediatr Neonatal Individ Med 2017; 6: e060126 DOI: 10.7363/060126.
- 2 Migliazza L, Bellan C, Alberti D. et al. Retrospective study of 111 cases of congenital diaphragmatic hernia treated with early high-frequency oscillatory ventilation and presurgical stabilization. J Pediatr Surg 2007; 42: 1526-1532 DOI: 10.1016/j.jpedsurg.2007.04.015.
- 3 Kipfmueller F, Schroeder L, Melaku T. et al. Prediction of ECMO and Mortality in Neonates with Congenital Diaphragmatic Hernia Using the SNAP-II Score. Klin Pädiatrie 2019; 231: 297-303 DOI: 10.1055/a-1009-6671.
- 4 Snoek KG, Greenough A, van Rosmalen J. et al. Congenital Diaphragmatic Hernia: 10-Year Evaluation of Survival, Extracorporeal Membrane Oxygenation, and Foetoscopic Endotracheal Occlusion in Four High-Volume Centres. Neonatology 2018; 113: 63-68 DOI: 10.1159/000480451.
- 5 Coughlin MA, Werner NL, Gajarski R. et al. Prenatally diagnosed severe CDH: mortality and morbidity remain high. J Pediatr Surg 2016; 51: 1091-1095 DOI: 10.1016/j.jpedsurg.2015.10.082.
- 6 Menon SC, Tani LY, Weng HY. et al. Clinical characteristics and outcomes of patients with cardiac defects and congenital diaphragmatic hernia. J Pediatr 2013; 162: 114-119.e2 DOI: 10.1016/j.jpeds.2012.06.048.
- 7 O’Brien SM, Clarke DR, Jacobs JP. et al. An empirically based tool for analyzing mortality associated with congenital heart surgery. J Thorac Cardiovasc Surg 2009; 138: 1139-1153 DOI: 10.1016/j.jtcvs.2009.03.071.
- 8 Russo FM, Eastwood MP, Keijzer R. et al. Lung size and liver herniation predict need for extracorporeal membrane oxygenation but not pulmonary hypertension in isolated congenital diaphragmatic hernia: systematic review and meta-analysis. Ultrasound Obstet Gynecol 2017; 49: 704-713 DOI: 10.1002/uog.16000.
- 9 Snoek KG, Reiss IKM, Greenough A. et al. Standardized postnatal management of infants with congenital diaphragmatic hernia in Europe: The CDH EURO Consortium Consensus – 2015 Update. Neonatology 2016; 110: 66-74 DOI: 10.1159/000444210.
- 10 Kinsella JP, Steinhorn RH, Mullen MP. et al. The Left Ventricle in Congenital Diaphragmatic Hernia: Implications for the Management of Pulmonary Hypertension. J Pediatr 2018; 197: 17-22 DOI: 10.1016/j.jpeds.2018.02.040.
- 11 Cordier AG, Russo FM, Deprest J. et al. Prenatal diagnosis, imaging, and prognosis in Congenital Diaphragmatic Hernia. Semin Perinatol 2020; 44: 51163 DOI: 10.1053/j.semperi.2019.07.002.
- 12 Yu PT, Jen HC, Rice-Townsend S. et al. The role of ECMO in the management of congenital diaphragmatic hernia. Semin Perinatol 2020; 44: 151166 DOI: 10.1053/j.semperi.2019.07.005.
- 13 Finer NM. Inhaled Nitric Oxide and Hypoxic Respiratory Failure in Infants With Congenital Diaphragmatic Hernia. Pediatrics 1997; 99: 838-845 doi:10.1542/peds.99.6.838
- 14 Putnam LR, Tsao K, Morini F. et al. Evaluation of Variability in Inhaled Nitric Oxide Use and Pulmonary Hypertension in Patients With Congenital Diaphragmatic Hernia. JAMA Pediatr 2016; 170: 1188 DOI: 10.1001/jamapediatrics.2016.2023.
- 15 Herich K, Schaible T, Reinhard J. et. al. iNO Therapy in Patients with Congenital Diaphragmatic Hernia – Discrepancy between Widespread Use and Therapeutic Effects. Klin Pädiatrie 2019; 231: 320-325 DOI: 10.1055/a-0991-0455.
- 16 Schaible T, Hermle D, Loersch F. et al. A 20-year experience on neonatal extracorporeal membrane oxygenation in a referral center. Intensive Care Med 2010; 36: 1229-1234 DOI: 10.1007/s00134-010-1886-5.
- 17 Bialkowski A, Moenkemeyer F, Patel N. Intravenous Sildenafil in the Management of Pulmonary Hypertension Associated with Congenital Diaphragmatic Hernia. Eur J Pediatr Surg 2013; 25: 171-176 doi:10.1055/s-0033-1357757
- 18 Cochius-den Otter S, Schaible T, Greenough A.u.a. The CoDiNOS trial protocol: an international randomised controlled trial of intravenous sildenafil versus inhaled nitric oxide for the treatment of pulmonary hypertension in neonates with congenital diaphragmatic hernia. BMJ Open 2019; 9: e032122 DOI: 10.1136/bmjopen-2019-032122.
- 19 Patel N, Massolo AC, Kipfmueller F. Congenital diaphragmatic hernia-associated cardiac dysfunction. Semin Perinatol 2020; 44: 151168 DOI: 10.1053/j.semperi.2019.07.007.
- 20 Patel N, Kipfmueller F. Cardiac dysfunction in congenital diaphragmatic hernia: Pathophysiology, clinical assessment, and management. Semin Pediatr Surg 2017; 26: 154-158 doi:10.1053/j.sempedsurg.2017.04.001
- 21 Patel N, Lally PA, Kipfmueller F. et al. Ventricular dysfunction is a critical determinant of mortality in congenital diaphragmatic hernia. Am J Respir Crit Care Med 2019; 200: 1522-1530 DOI: 10.1164/rccm.201904-0731OC.
- 22 Guner YS, Harting MT, Fairbairn K. et al. Outcomes of infants with congenital diaphragmatic hernia treated with venovenous versus venoarterial extracorporeal membrane oxygenation: A propensity score approach. J Pediatr Surg 2018; 53: 2092-2099 DOI: 10.1016/j.jpedsurg.2018.06.003.
- 23 Douflé G, Roscoe A, Billia F. u. a Echocardiography for adult patients supported with extracorporeal membrane oxygenation. Crit Care 2015; 19: 1-10 DOI: 10.1186/s13054-015-1042-2.
- 24 Gewillig M. THE FONTAN CIRCULATION. Heart 2005; 91: 839-846 DOI: 10.1136/hrt.2004.051789.
- 25 Akintürk H, Michel-Behnke I, Valeske K. et. al. Hybrid Transcatheter–Surgical Palliation. Pediatr Cardiol 2007; 28: 79-87 doi:10.1007/s00246-006-1444-7
- 26 Tchervenkov CI, Tahta SA, Jutras LC. et al. Biventricular repair in neonates with hypoplastic left heart complex. Ann Thorac Surg 1998; 66: 1350-1356 DOI: 10.1016/S0003-4975(98)00803-0.
- 27 Schranz D, Bauer A, Reich B. et. al. Fifteen-year Single Center Experience with the “Giessen Hybrid” Approach for Hypoplastic Left Heart and Variants: Current Strategies and Outcomes. Pediatr Cardiol 2015; 36: 365-373 DOI: 10.1007/s00246-014-1015-2.
- 28 Okawada M, Yanai T, Yamataka A. et al. Congenital diaphragamatic hernia associated with aortic coarctation: a case report. Cases J 2008; 1: 378 DOI: 10.1186/1757-1626-1-378.