Brennan Report - Department of Health and Children
Brennan Report - Department of Health and Children Brennan Report - Department of Health and Children
Report of the Commission on Financial Management and Control Systems in the Health ServiceIn our view, the operation of the Drugs Payment Scheme needs to be urgently reviewed. Atpresent there is no incentive comparable to the GMS to encourage the prescriber (GP,Consultant or Non-Consultant Hospital Doctor) to prescribe products that may be just aseffective but considerably cheaper than high-cost brands. Furthermore, where a doctorprescribes the more expensive product, the profits of retail pharmacies are increased.We recommend that a review be undertaken to ensure that this expenditure is economic, costeffective and provides value for money. Controlling pharmaceutical costs is animportant, though complex, management process and will require collaboration between theDepartment of Health and Children, health boards and medical/pharmacy professionals. Keyfeatures of this review will include:●●●●●Influencing/incentivising positive prescriber behaviour;Minimising inappropriate prescribing;Maximising the prescription and dispensing of generic products;Negotiating cost competitive drug prices at national level; andImplementing common hospital/primary care drug formularies.We consider that this review should apply across all publicly-funded drugs and medicinesschemes – medical card scheme, Drugs Payment Scheme, Long Term Illness Scheme and HighTech Medicines Scheme.We believe that a flat-fee basis for reimbursement of drug costs by the GMS (Payments) Boardto pharmacists should apply across all national drug schemes. In addition, the State should onlyreimburse at the rate of the lowest cost for therapeutically equivalent products in allschemes.Recommendations relating to the Drugs Payment SchemeR6.11 Current arrangements for reimbursing pharmacists under the medical card scheme – i.e. reimbursement on acost of ingredients basis (without mark-up) plus a flat-rate prescription fee – should be extended to the DrugsPayment Scheme.R6.12 The operation of the Drugs Payment Scheme should be reviewed immediately by the Department of Health andChildren, in consultation with the Department of Finance, the GMS (Payments) Board and the health boards. Thereview should actively examine:(i) Introducing a system whereby health boards would actively monitor and evaluate prescribing patterns byindividual GPs, Consultants or Dentists and reimbursement patterns by individual pharmacists, havingregard to relevant demographic and epidemiological factors;(ii)(iii)(iv)Introducing incentive schemes for reducing levels of prescribing and drugs costs;In recognition of the influence of hospital generated prescribing on community drugs budgets, each healthboard/hospital CEO should immediately establish Drugs and Therapeutics Committees, comprisingConsultants, GPs from the hospital catchment area, supported by pharmacy and financial managementexpertise, to agree clinically cost-effective common drug formulary; andRelevant international experience and the lessons from this in containing drug costs and the rate ofgrowth.R6.13 The existing agreement between the Department of Health and Children and the Irish PharmaceuticalHealthcare Association should be evaluated against international experience with similar agreements(particularly in countries of the European Union). The results of this evaluation should be used in thenegotiation of any further agreement so as to assure value for money.84
Chapter 6 Accountability – General Medical Services and Community Drug SchemesNew products continually come on the market. These products are usually more expensivethan existing treatments and are patent-protected so that generic substitution is not possible.If prescribed in substitution for existing, lower priced drugs, they will have an escalating impacton the drug budget. Products of differing price may have similar content.We recognise that since 1998 work has been ongoing on economic evaluation ofpharmaceuticals. Economic evaluations have been conducted on a number of medicines, and thenational centre has negotiated a framework for economic evaluation with the pharmaceuticalindustry. The centre has provided information to prescribers through the medical press,highlighting expenditure trends in the community drug schemes, and suggesting improvementsin regard to the cost-effectiveness of prescribing.Recommendations relating to Drugs AssessmentR6.14 The Irish Medicines Board should have its remit extended to not just examine new drugs for their efficacy andeffectiveness, but also to:(i) Assess their cost effectiveness; and(ii) Approve the drug product for reimbursement under the community drugs schemes (including specifyingthe conditions under which it may be made available, for example restricted to named patients or inrespect of defined clinical treatment regimes).R6.15 The Irish Medicines Board should also be charged with the responsibility to monitor the continuing effectivenessof existing drugs and to delist those which are no longer considered appropriate or clinically cost-effective.R6.16 Where the Irish Medicines Board determines that a cheaper, but equally effective, alternative exists, only the costof the cheaper drug should be reimbursed by the GMS (Payments) Board. Where a GP prescribes the moreexpensive branded drug, the cost difference arising should be regarded as entirely private prescribing.6.5 SUMMARYIn this Chapter, we have identified the medical card and community drug schemes as thearea showing the greatest cost escalation in recent years.Mirroring the approach taken in Chapter 5 in respect of Consultants and General Managers, wehave recommended that, again consistent with our core principle of personal accountability, GPsbe designated as the fundamental unit of accountability in relation to the medical card scheme.We also make recommendations to address the gaps in evaluation, benchmarking andmanagement of the various drugs schemes from a value for money perspective. Some of theseproblems were illustrated in our description of inaccurate costings and records within theGeneral Medical Services in Chapter 2.85
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<strong>Report</strong> <strong>of</strong> the Commission on Financial Management <strong>and</strong> Control Systems in the <strong>Health</strong> ServiceIn our view, the operation <strong>of</strong> the Drugs Payment Scheme needs to be urgently reviewed. Atpresent there is no incentive comparable to the GMS to encourage the prescriber (GP,Consultant or Non-Consultant Hospital Doctor) to prescribe products that may be just aseffective but considerably cheaper than high-cost br<strong>and</strong>s. Furthermore, where a doctorprescribes the more expensive product, the pr<strong>of</strong>its <strong>of</strong> retail pharmacies are increased.We recommend that a review be undertaken to ensure that this expenditure is economic, costeffective <strong>and</strong> provides value for money. Controlling pharmaceutical costs is animportant, though complex, management process <strong>and</strong> will require collaboration between the<strong>Department</strong> <strong>of</strong> <strong>Health</strong> <strong>and</strong> <strong>Children</strong>, health boards <strong>and</strong> medical/pharmacy pr<strong>of</strong>essionals. Keyfeatures <strong>of</strong> this review will include:●●●●●Influencing/incentivising positive prescriber behaviour;Minimising inappropriate prescribing;Maximising the prescription <strong>and</strong> dispensing <strong>of</strong> generic products;Negotiating cost competitive drug prices at national level; <strong>and</strong>Implementing common hospital/primary care drug formularies.We consider that this review should apply across all publicly-funded drugs <strong>and</strong> medicinesschemes – medical card scheme, Drugs Payment Scheme, Long Term Illness Scheme <strong>and</strong> HighTech Medicines Scheme.We believe that a flat-fee basis for reimbursement <strong>of</strong> drug costs by the GMS (Payments) Boardto pharmacists should apply across all national drug schemes. In addition, the State should onlyreimburse at the rate <strong>of</strong> the lowest cost for therapeutically equivalent products in allschemes.Recommendations relating to the Drugs Payment SchemeR6.11 Current arrangements for reimbursing pharmacists under the medical card scheme – i.e. reimbursement on acost <strong>of</strong> ingredients basis (without mark-up) plus a flat-rate prescription fee – should be extended to the DrugsPayment Scheme.R6.12 The operation <strong>of</strong> the Drugs Payment Scheme should be reviewed immediately by the <strong>Department</strong> <strong>of</strong> <strong>Health</strong> <strong>and</strong><strong>Children</strong>, in consultation with the <strong>Department</strong> <strong>of</strong> Finance, the GMS (Payments) Board <strong>and</strong> the health boards. Thereview should actively examine:(i) Introducing a system whereby health boards would actively monitor <strong>and</strong> evaluate prescribing patterns byindividual GPs, Consultants or Dentists <strong>and</strong> reimbursement patterns by individual pharmacists, havingregard to relevant demographic <strong>and</strong> epidemiological factors;(ii)(iii)(iv)Introducing incentive schemes for reducing levels <strong>of</strong> prescribing <strong>and</strong> drugs costs;In recognition <strong>of</strong> the influence <strong>of</strong> hospital generated prescribing on community drugs budgets, each healthboard/hospital CEO should immediately establish Drugs <strong>and</strong> Therapeutics Committees, comprisingConsultants, GPs from the hospital catchment area, supported by pharmacy <strong>and</strong> financial managementexpertise, to agree clinically cost-effective common drug formulary; <strong>and</strong>Relevant international experience <strong>and</strong> the lessons from this in containing drug costs <strong>and</strong> the rate <strong>of</strong>growth.R6.13 The existing agreement between the <strong>Department</strong> <strong>of</strong> <strong>Health</strong> <strong>and</strong> <strong>Children</strong> <strong>and</strong> the Irish Pharmaceutical<strong>Health</strong>care Association should be evaluated against international experience with similar agreements(particularly in countries <strong>of</strong> the European Union). The results <strong>of</strong> this evaluation should be used in thenegotiation <strong>of</strong> any further agreement so as to assure value for money.84