Characteristics of drugs for which clinical pharmacogenetic testing may be considered [43] | |
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Significant inter-individual variability in drug response Narrow therapeutic range Potential for severe adverse effects Development of treatment resistance Need for long-term treatment High cost of the medication |
Consideration points for clinical pharmacogenetic testing | |
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Correlation between genotype and phenotype (predictive power for drug response) | The degree of correlation between genetic variants and drug response outcomes should be well established. |
Clear and sufficient evidence of clinical utility | There must be robust evidence supporting the clinical usefulness of pharmacogenetic testing, such as large-scale studies, randomized controlled trials, and meta-analyses. |
Standardized guidelines for drug selection and dosage adjustment based on pharmacogenetic profiles | There should be clear, standardized guidelines on how to use pharmacogenomic information to select drugs and adjust dosages. |
Genotypic and phenotypic variability by ethnicity or race | Information on the types and distribution of alleles and genotypes across different ethnic or racial groups should be available. |
Technical feasibility and analytical capability of testing methods | The ease of use, expected analytical performance, and cost of testing should be considered. |
Comprehensive interpretation by experts | The ability to provide thorough result interpretation should be supported by adequate knowledge and experience in various fields, such as medicine, clinical pharmacology, clinical genetics, and laboratory medicine. |
Turnaround time for results | The time required to obtain test results should align with the clinical indications and requirements of the healthcare environment. |
Cost-effectiveness | The clinical utility of the test should justify its cost, with a favorable balance between test expenses and the benefits gained. |
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