COST-MINIMIZATION ANALYSIS FOR DETERMINATION OF GENETIC POLYMORPHISMS IN CLINICAL PRACTICE
Author(s)
García Gil S1, Ramos Díaz R2, Nazco Casariego GJ1, Viña Romero MM3, Pérez Pérez JA4, Gutiérrez Nicolás F1
1Complejo Hospitalario Universitario de canarias, San Cristobal de La Laguna, Spain, 2FUNCANIS, San Cristóbal de La Laguna, Spain, 3Hospital Universitario Nuestra Señora de La Candelaria, Santa Cruz de Tenerife, Spain, 4Universidad de La Laguna, San Cristóbal de La Laguna, Spain
OBJECTIVES: To compare polymerase chain reaction (PCR)-sequencing method and real time PCR (rtPCR) with HybProbe® fluorescent probes method, using a cost minimization analysis to determine the lower-cost method for the intentification of genetic polymorphisms in clinical practice. METHODS: The cost-minimization calculator was designed using Excel®2003. Direct cost derived from the SNP(Simple Nucleotide Polymorphism) determination were compared between two methods: Method1: Amplification by PCR and sequencing Method2: rtPCR and HybProbe® with allele-specific fluorescent probes determination. Reigistered variables for sensitivity analysis were: SNPs to be determined, monthly samples and sequencing-price. Base case was performed with: 22 monthly patients, with 34 SNPs by patient, during two years and a sequencing cost of 5€ per determination. The sensitivity analysis was done with: cost sequencing between 2-7 €; number of patients between 5 and 40; and a number of SNP determinations between 5 and 60. RESULTS: The base case would involve a cost of: 101,944.5€ for method 1(212.4€/ patient) and 20,118.6 € for method 2 (41.9€ / patient ). The sensitivity analysis showed that a reduction of 60% in the sequencing cost would reduce the method 2 cost to 52,984.5€. To reduce SNPs to 5: method 1:
Conference/Value in Health Info
2018-09, ISPOR Asia Pacific 2018, Tokyo, Japan
Value in Health, Vol. 21, S2 (September 2018)
Code
PCN59
Topic
Economic Evaluation
Topic Subcategory
Cost-comparison, Effectiveness, Utility, Benefit Analysis
Disease
Oncology
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