Table 1.
Themes | Actions | Responsible stakeholder(s) |
---|---|---|
Division of responsibilities | *Develop a national guideline on collaboration. | Health care provider organizations of pharmacists and GPs (KNMP/NHG). |
Make agreements on a regional level about when and who can request PGx tests. | Regional groups for pharmacotherapeutic consultation (local organization of GPs and pharmacists). | |
Data registration and sharing | *Define relevant data that should be registered and shared between health care professionals for effective use of PGx. | Health care provider organizations of pharmacists and GPs (KNMP/NHG). |
*Standardize patient data that needs to be registered with regard to PGx. | Health care provider organizations of pharmacists and GPs (KNMP/NHG) and NICTIZ (National IT Institute in Health Care). | |
Further develop the National Link Point to enable easy exchange of PGx data between health care professionals. | VZVZ (Association of health care providers for health communication) at the initiative of the health care provider organizations (KNMP/NHG) in collaboration with NICTIZ (National IT Institute in Health Care). | |
Facilitate aligned registration for the reason of adjusting a patient’s treatment regime, to monitor and evaluate effectiveness of applying PGx. | NICTIZ (National IT Institute in Health Care), in collaboration with software developers HIS/AIS (information systems for GPs/pharmacists), at the initiative of the Dutch GP association (LHV)/Royal Dutch Pharmacists Association (KNMP). | |
Adjust or develop software systems to facilitate applying PGx. | Software developers HIS/AIS (information systems for GPs/pharmacists), at the initiative of the Dutch GP association (LHV)/Royal Dutch Pharmacists Association (KNMP), in collaboration with NICTIZ (National IT Institute in Health Care). | |
Generating evidence for guideline development | *Gather data on the number of prevented ineffective or adverse drug responses through PGx. | Funders for research/independent research institutes/scientific organizations. |
*Validate the predictive value of PGx tests through prospective or observational research. | Scientific organizations. | |
*Assess the cost saving of PGx test through pharmaco-economic studies. | Scientific organizations. | |
*Collect data on the impact on clinical outcomes by assessing the patient experience of the severity of ineffective or adverse drug response. | Scientific organizations, together with patient organizations. | |
*Develop aligned patient information on the benefit of PGx tests. Monitor data on the frequency of genetic variants that are tested with PGx. | Health care provider organizations (KNMP/NHG) of pharmacists and GPs together with patient organizations Independent research institutes. | |
Monitor data on the frequency of genetic variants that are tested with PGx. | Independent research institutes. | |
Reimbursement | *Include PGx tests as an optional test for general practitioners in their guideline. | Dutch organization for general practitioners (NHG). |
Develop aligned patient information on the costs of PGx test and the impact on their health care insurance reimbursement. | Health care provider organizations of pharmacists and GPs (KNMP/NHG), in collaboration with ZN (Dutch Health Care Insurers) and patient organizations. | |
Define and prioritize disease areas eligible for reimbursement based on data on clinical utility. | Health insurers and ZINl (Dutch Health Care Institute). |
Statements preceded by an asterisk (*) remained after three iterations of the Delphi procedure. PGx pharmacogenetics, GP general practitioner.