Cost-effective analysis of screening for biliary atresia with the stool color card

Douglas Mogul1, Mo Zhou, Paul Intihar

  • 1*Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Johns Hopkins University School of Medicine †Department of Health Policy and Management, Johns Hopkins University School of Public Health ‡Department of Financial Analysis, Johns Hopkins Hospital §Johns Hopkins Carey Business School, Baltimore, MD.

Insights

Screening for biliary atresia (BA) using a stool color card is a cost-saving strategy. This method improves outcomes by reducing deaths and liver transplants, making it economically feasible for the United States.

Area of Science:

  • Pediatric Gastroenterology and Hepatology
  • Health Economics and Outcomes Research
  • Public Health Screening

Background:

  • Biliary atresia (BA) is a primary cause of pediatric end-stage liver disease and liver transplantation in the US.
  • Delayed diagnosis of BA leads to poorer outcomes, including increased mortality and need for transplantation.
  • Early detection is crucial for improving patient prognosis and reducing healthcare burdens.

Purpose of the Study:

  • To evaluate the cost-effectiveness of nationwide screening for biliary atresia (BA) using a stool color card in the United States.
  • To compare the outcomes and costs of BA screening versus no screening over a 20-year period.
  • To determine if stool color card screening is a dominant strategy in managing BA.

Main Methods:

  • A 20-year Markov model simulated the natural history and transplant outcomes of BA patients in the US.
  • Data on health states, transplant rates, and mortality were sourced from published literature.
  • Costs were estimated using literature data and the Johns Hopkins database; screening strategy B utilized a Taiwan-developed stool color card.

Main Results:

  • Nationwide screening (Strategy B) was projected to cost $133.9 million over 20 years, compared to $142.5 million for no screening (Strategy A).
  • Screening is associated with improved outcomes: 3731.7 life-years gained, 71 deaths, and 147 liver transplants, versus 3702 life-years, 74 deaths, and 158 transplants without screening.
  • There is a >97% probability that stool color card screening is cost-saving and increases life-years gained, with specificity being the key parameter.

Conclusions:

  • Screening for biliary atresia (BA) using a stool color card is a dominant strategy, offering lower costs and better patient outcomes compared to no screening.
  • This approach represents an economically feasible method to improve BA management and outcomes in the US.
  • The findings support the implementation of stool color card screening as a vital public health initiative for pediatric liver disease.
Abstract

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