Assessment of pulmonary artery size at birth as a prognostic factor in congenital diaphragmatic hernia: results of a multicenter study in Japan
Author:
Funder
The Ministry of Health, Labour, and Welfare of Japan. Granted/Award Number: H24-Nanchi-Ippan-034
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health
Link
https://www.nature.com/articles/s41372-023-01750-0.pdf
Reference22 articles.
1. Bagolan P, Morini F. Long-term follow up of infants with congenital diaphragmatic hernia. Semin Pediatr Surg. 2007;16:134–44.
2. Grover TR, Murthy K, Brozanski B, Gien J, Rintoul N, Keene S, et al. Children’s Hospitals Neonatal Consortium: Short-term outcomes and medical and surgical interventions in infants with congenital diaphragmatic hernia. Am J Perinatol. 2015;32:1038–44.
3. Boloker J, Bateman DA, Wung JT, Stolar CJ. Congenital diaphragmatic hernia in 120 infants treated consecutively with permissive hypercapnia/spontaneous respiration/elective repair. J Pediatr Surg. 2002;37:357–66.
4. Kitano Y, Nakagawa S, Kuroda T, Honna T, Ito Y, Nakamura T, et al. Liver position in fetal congenital diaphragmatic hernia retains a prognostic value in the era of lung-protective strategy. J Pediatr Surg. 2005;40:1827–32.
5. Lusk LA, Wai KC, Moon-Grady AJ, Basta AM, Filly R, Keller RL. Fetal ultrasound markers of severity predict resolution of pulmonary hypertension in congenital diaphragmatic hernia. Am J Obstet Gynecol. 2015;213:e211–e218.
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