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Zani, A., Eaton, S., Morini, F., Puri, P., Rintala, R., Heurn, E., Lukac, M., Bagolan, P., Kuebler, J., Friedmacher, F., Wijnen, R., Tovar, J., Hoellwarth, M. and Pierro, A. (2017) European Paediatric Surgeons’ Association Survey on the Management of Hirschsprung Disease. European Journal of Pediatric Surgery, 27, 96-101.
https://doi.org/10.1055/s-0036-1593991

has been cited by the following article:

• TITLE: Review. Gastrointestinal Surgery in Neonates: Practice, Facts, and Trends

  AUTHORS: Ralf-Bodo Tröbs

  KEYWORDS: Neonatal Surgery, Acute Abdomen, Gastrointestinal Atresia, Necrotizing Enterocolitis, Bowel Obstruction

  JOURNAL NAME: Open Journal of Pediatrics, Vol.9 No.2, June 18, 2019

  ABSTRACT: The author presents an overview of the current trends in acute neonatal gastrointestinal surgery. Necrotizing enterocolitis and focal intestinal perforation are disorders of different etiology, appearance, and prognosis. In neonates with focal perforation, a good prognosis can be expected. Primary anastomosis is a valid option for primary surgery. Meconium ileus is based on obstruction of the terminal ileum. Medical treatment is the primary therapeutic option, although surgery may be required. In contrast, meconium plug syndrome is based on stool plugging in the left colon, and surgery is not appropriate. Hirschsprung’s disease is confirmed on the basis of representative biopsy of the rectum just above the dentate line. There is a trend toward a single-step pull-through operation without protective stoma. Open hernia repair in small neonates can be performed via a mini-incision and without opening the external inguinal ring. Laparoscopic hernia repair has some advantages, especially in girls. In infants with pyloric stenosis, laparoscopic pyloromyotomy is a first line option for treatment. There is a general trend toward single-stage procedures and laparoscopic reconstructive surgery for gastrointestinal malformations. With the exception of tracheoesophageal fistula and low bowel obstruction, the vast majority of upper gastrointestinal malformations can be identified using prenatal ultrasound examination. One-stage repair with excellent results is even possible in neonates below 1000 g. Surgery of duodenal or small bowel atresia can be performed following the postnatal adaptation period. For some forms of anorectal malformation, the need for a protective stoma has been questioned in the last decade. Posterior sagittal anorectoplasty remains the standard procedure for the majority of cases. Midgut or segmental volvulus affects different groups of infants. If a neonate is suspected of having any type of volvulus, urgent surgery is required. Intestinal duplication carries a high risk for complications, and surgery should be performed on an elective basis.