Abstract

Background: Stool color card (SCC) screenings for biliary atresia (BA) have shown to improve Kasai timing and outcome significantly. Both obligatory and non-obligatory screenings with passive distribution strategies have proven to be effective. Therefore, we have initiated a voluntary SCC program and aim to describe our experience. Methods: Since 2017 we supply all maternity wards in Lower-Saxony with SCC. Attending pediatricians and parents of BA infants were contacted via questionnaires and asked for their evaluation of the SCC screening. Results: 85.2% of attending pediatricians support the SCC screening, but only 78.1% considered the initiative useful. In their clinical routine, only 67% of visiting parents report to have received an SCC at the maternity hospital. In the group of parents of BA infants, only 54% (7/13) had received an SCC. Out of those seven parents, only one had referred their child to a children’s hospital based on pathological SCC results. The lack of SCC education in the maternity hospitals was made responsible by parents. Within three years, only one infant with BA was identified through the SCC. Conclusions: Our voluntary SCC screening shows serious limitations with inacceptable distribution of SCCs and low acceptance of attending pediatricians. SCC programs in decentralized health care systems without educational campaigns, standardized diagnostic and treatment algorithms and the definition of reference centers are additional burdens for local health care providers without the promised benefit.

Highlights

  • For infants with biliary atresia (BA) the Kasai procedure (KPE) offers a limited chance for survival with native liver

  • In Asia, with the highest global BA incidence, the idea of a mass screening for biliary atresia was already discussed in the 1980s and led to the stool color card (SCC) screening model that was established in the Japanese Tochigi Prefecture in 1994 [3,4]

  • Only two-thirds of parents reported during the first regular check-ups of their child that they had received an SCC with their Child Health booklet in the maternity hospital

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Summary

Introduction

For infants with biliary atresia (BA) the Kasai procedure (KPE) offers a limited chance for survival with native liver. All programs have in common, that they reported on earlier Kasai-procedures [11] Those studies were complemented by cost- and health-effectiveness analysis, suggesting that SCC screenings in countries with high and low BA incidences improve BA outcomes, but include savings in terms of healthcare expenditure [11,12]. Stool color card (SCC) screenings for biliary atresia (BA) have shown to improve Kasai timing and outcome significantly. Both obligatory and non-obligatory screenings with passive distribution strategies have proven to be effective. Results: 85.2% of attending pediatricians support the SCC screening, but only 78.1% considered the initiative useful In their clinical routine, only 67% of visiting parents report to have received an SCC at the maternity hospital. SCC programs in decentralized health care systems without educational campaigns, standardized diagnostic and treatment algorithms and the definition of reference centers are additional burdens for local health care providers without the promised benefit

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