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Original Article

Budget impact analysis on the introduction of a guideline based hepatitis B and C screening into a routine check-up in the German primary care setting

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Pages 76-82 | Received 21 Jul 2017, Accepted 03 Oct 2017, Published online: 24 Oct 2017
 

Abstract

Objectives: Systematic screening for chronic hepatitis B and C does not yet exist in Germany. Therefore, the implementation of a screening approach within a preventive medical examination performed by primary care physicians (‘Check-Up 35+’) was evaluated in a recent prospective multicenter study. The present analysis estimates the financial consequences for the statutory health insurance by budget impact analysis.

Materials and methods: A Markov cohort model was developed consisting of 21 health states. Four different screening scenarios derived from the previous multicenter study were compared to usual care, a strategy without screening for hepatitis. Actual cost data for Germany were calculated and systematic literature searches for all input parameters were performed.

Results: The base case results in incremental costs for the screening strategies compared to no hepatitis screening of 165–227 € per patient in a 20-year horizon. Two main parameters influence the financial consequences: (A) detection and treatment increase the costs in the beginning. (B) Screening avoids hepatitis induced end-stage liver disease. The initial higher costs exceed the later savings. Sensitivity analyses demonstrate a strong impact of medication costs for the treatment of additionally detected hepatitis infections on the outcome. This finding is robust to sensitivity analysis.

Conclusions: The screening strategy proposed here implies additional costs for the statutory health insurance, however, a decision regarding its usefulness must consider criteria other than cost. For example, the high burden of disease due to liver cirrhosis and liver carcinoma should be considered. Therefore, an additional cost-effectiveness-analysis should be conducted.

Acknowledgements

The project was funded by unrestricted research grants from Gilead Sciences, Abbvie, Bristol-Myers Squibb, and MSD to Thomas Berg.

Disclosure statement

Johannes Wiegand has served as a speaker, a consultant, and an advisory board member for AbbVie, BMS, Boehringer, Gilead, Janssen, Roche, Intercept and Siemens, and has received research funding from Siemens and GlaxoSmithKline.

Thomas Berg has served as a speaker, a consultant, and an advisory board member for AbbVie, BMS, Boehringer, Gilead, Intercept, Janssen, Merck, Novartis, Roche, and Vertex Pharmaceuticals Incorporated, and has received research funding from Gilead, Abbvie, Bristol-Myers Squibb, MSD, Janssen, Novartis, and Roche.

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