Surgical Strategies for Neonates with Prenatally Diagnosed Congenital Biliary Dilatation.

Choledochal cyst Congenital biliary dilatation Prenatal diagnosis

Journal

Journal of pediatric surgery
ISSN: 1531-5037
Titre abrégé: J Pediatr Surg
Pays: United States
ID NLM: 0052631

Informations de publication

Date de publication:
20 Oct 2023
Historique:
received: 04 10 2023
accepted: 14 10 2023
medline: 16 11 2023
pubmed: 16 11 2023
entrez: 15 11 2023
Statut: aheadofprint

Résumé

This study aimed to develop a postnatal treatment strategy for infants with prenatally diagnosed congenital biliary dilatation. We performed a retrospective study of patients with prenatal diagnosed congenital biliary dilatation (CBD), aged <1 year who underwent surgery at our hospital between 2013 and 2023. We classified the patients into two groups, the "early group," consisting of patients who could not wait for growth, and required early surgery, and the "scheduled group," consisting of patients who were asymptomatic and could undergo scheduled surgery, and compared them. The parameters for early surgical prediction were AST, ALT, TB, DB, and CRP levels at birth, 1 week, 2 weeks, 1 month, 2 months, and 3 months after birth, and immediately before surgery, as well as the cyst diameter, presence of intrahepatic bile duct dilation, and presence of debris in the common bile duct. During the study period, 15 patients were diagnosed prenatally. The cyst diameter was significantly larger at all points in the early group. Patients with a cyst diameter of >30 mm at birth, intrahepatic bile duct dilatation at birth, and postnatal enlargement of the common bile duct to >30 mm are more likely to develop symptoms early. Blood biochemistry tests showed no significant differences between the two groups. Patients with a cyst diameter >30 mm in the early postnatal period require careful postnatal management and parents should be counseled regarding the high likelihood of their child needing surgery within the first 3 months of life. Level IV.

Sections du résumé

BACKGROUND BACKGROUND
This study aimed to develop a postnatal treatment strategy for infants with prenatally diagnosed congenital biliary dilatation.
METHODS METHODS
We performed a retrospective study of patients with prenatal diagnosed congenital biliary dilatation (CBD), aged <1 year who underwent surgery at our hospital between 2013 and 2023. We classified the patients into two groups, the "early group," consisting of patients who could not wait for growth, and required early surgery, and the "scheduled group," consisting of patients who were asymptomatic and could undergo scheduled surgery, and compared them. The parameters for early surgical prediction were AST, ALT, TB, DB, and CRP levels at birth, 1 week, 2 weeks, 1 month, 2 months, and 3 months after birth, and immediately before surgery, as well as the cyst diameter, presence of intrahepatic bile duct dilation, and presence of debris in the common bile duct.
RESULTS RESULTS
During the study period, 15 patients were diagnosed prenatally. The cyst diameter was significantly larger at all points in the early group. Patients with a cyst diameter of >30 mm at birth, intrahepatic bile duct dilatation at birth, and postnatal enlargement of the common bile duct to >30 mm are more likely to develop symptoms early. Blood biochemistry tests showed no significant differences between the two groups.
CONCLUSIONS CONCLUSIONS
Patients with a cyst diameter >30 mm in the early postnatal period require careful postnatal management and parents should be counseled regarding the high likelihood of their child needing surgery within the first 3 months of life.
LEVEL OF EVIDENCE METHODS
Level IV.

Identifiants

pubmed: 37968151
pii: S0022-3468(23)00655-3
doi: 10.1016/j.jpedsurg.2023.10.045
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declarations of interest None.

Auteurs

Chiyoe Shirota (C)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan. Electronic address: cshirota@med.nagoya-u.ac.jp.

Akinari Hinoki (A)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Takahisa Tainaka (T)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Wataru Sumida (W)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Satoshi Makita (S)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Hizuru Amano (H)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Aitaro Takimoto (A)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Akihiro Yasui (A)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Yoichi Nakagawa (Y)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Jiahui Liu (J)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Yaohui Guo (Y)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Daiki Kato (D)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Yousuke Goda (Y)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Takuya Maeda (T)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Hiroo Uchida (H)

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Classifications MeSH