» Articles » PMID: 29862332

Newborn Biliary Atresia Screening with the Stool Colour Card: a Questionnaire Survey of Parents

Overview
Specialty Pediatrics
Date 2018 Jun 5
PMID 29862332
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: Biliary atresia can easily be screened using a stool colour card (SCC) and has shown to significantly reduce time to diagnosis, improving children's outcome. Despite the general approval of the clinical usefulness of the SCC, physicians remain reluctant: it might unnecessarily worry parents. This study aimed to analyse the parental reaction to this screening method and if it evokes parental stress.

Methods: A semistructured questionnaire was sent to parents with one or more healthy child to inquire about reactions on receipt and use of the SCC.

Results: 109/256 questionnaires were returned and evaluated (43%). 107/107 parents considered the SCC as helpful, a simple screening method and easy to use (100%). 26/43 were reassured when receiving the SCC (60%), 2 were worried (5%) and 9 had no particular feelings (21%). In 41/49, emotions experienced during its use were positive or neutral (84%), and 3 were worried (6%). In 41/50, the discussion with the paediatrician about stool colour-linked pathologies was neutral (82%), and 9 felt uneasy (18%).

Conclusion: A vast majority of parents appreciate the SCC. It creates uneasiness in a minority of parents. Our results are encouraging and argue in favour of implementing the regular distribution of the SCC in antenatal, postnatal and newborn infant clinics.

Citing Articles

Editorial: Elimination of biliary atresia.

Kotb M, Ieiri S, Shehata S Front Pediatr. 2023; 11:1202727.

PMID: 37284287 PMC: 10241068. DOI: 10.3389/fped.2023.1202727.


Biliary Atresia in 2021: Epidemiology, Screening and Public Policy.

Schreiber R, Harpavat S, Hulscher J, Wildhaber B J Clin Med. 2022; 11(4).

PMID: 35207269 PMC: 8876662. DOI: 10.3390/jcm11040999.


Province-Wide Stool Color Card Screening for Biliary Atresia in Lower-Saxony: Experiences with Passive Distribution Strategies and Results.

Madadi-Sanjani O, Kuebler J, Uecker M, Pfister E, Baumann U, Kunze-Hullmann B Int J Neonatal Screen. 2021; 7(4).

PMID: 34842600 PMC: 8629020. DOI: 10.3390/ijns7040075.


A retrospective study of the ideal operation time for preterm biliary atresia patients.

Jiao C, Yu K, Li D, Fu K, Wang P, He Y Pediatr Surg Int. 2019; 35(6):679-684.

PMID: 30805663 DOI: 10.1007/s00383-019-04464-7.

References
1.
Mowat A, Davidson L, Dick M . Earlier identification of biliary atresia and hepatobiliary disease: selective screening in the third week of life. Arch Dis Child. 1995; 72(1):90-2. PMC: 1510987. DOI: 10.1136/adc.72.1.90. View

2.
Chang M . Screening for biliary atresia. Chang Gung Med J. 2006; 29(3):231-3. View

3.
Serinet M, Wildhaber B, Broue P, Lachaux A, Sarles J, Jacquemin E . Impact of age at Kasai operation on its results in late childhood and adolescence: a rational basis for biliary atresia screening. Pediatrics. 2009; 123(5):1280-6. DOI: 10.1542/peds.2008-1949. View

4.
Sokol R, Shepherd R, Superina R, Bezerra J, Robuck P, Hoofnagle J . Screening and outcomes in biliary atresia: summary of a National Institutes of Health workshop. Hepatology. 2007; 46(2):566-81. PMC: 3888317. DOI: 10.1002/hep.21790. View

5.
Matsui A, Ishikawa T . Identification of infants with biliary atresia in Japan. Lancet. 1994; 343(8902):925. DOI: 10.1016/s0140-6736(94)90052-3. View