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The James A Vohs Award Spring 2000 / Vol 4, No 2 |
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Achieving
Positive Outcomes through Collaborative Pharmaceutical Care: The KPNW
Medication Management Program Background Implementing the MMP required not only pharmacy department and delivery system modifications but a considerable culture change--change that KPNW planned for by designing a staged implementation strategy, focusing first on the single quality target and disease state of lipid management. In its first seven months of operation, MMP gains put KPNW in second position of all reporting KP Regions for lipid measurement (77%) and, more important, in the lead position of reporting KP Regions for lipid management (65.6%, 1998 HEDIS) (Figures 1 and 2). MMP also significantly improved drug utilization and reduced drug costs while improving quality. Objectives
KPNW hypothesized that standardized, centrally managed, population-based clinical pharmacy services, integrated into local health care teams and the delivery system, would improve quality of care, health outcomes, and reduce cost of drug therapies compared with drug therapies provided under the previous model. The
Process In 1996, the KPNW Regional Pharmacy Department initiated a quality improvement project to: 1) evaluate clinical pharmacy service delivery models inside and outside of KP, 2) evaluate the strengths and weaknesses of the current 'reactive' process of providing clinical pharmacy services, and 3) identify quality attributes and service features critical to a new model for the delivery of pharmaceutical care. Although no single best model emerged, the Pharmacy Department, in collaboration with Northwest Permanente physicians, Health Plan, and KPNW clinical committees, used the identified best practices to design the population-based MMP model. The Northwest Permanente physicians involved in the process were instrumental in soliciting support from fellow physicians, without whom MMP would not have been a success. Cardiovascular Steering Committee leaders helped to hone the focus for the initial stage of the implementation plan to an emphasis on high-risk, secondary-prevention patients. Other KPNW clinical committees continue to help focus priorities and shape the MMP program in vital, ongoing ways. Eight key best practices emerged for the new MMP model:
By yearend 1997, the new model was endorsed by the KPNW Operations Group and supported by pharmacists, medical staff, nurses, pharmacy managers, and other KPNW administrators. MMP began providing care in Spring 1998. MMP work contributes directly to the results of two KPNW-designated highest-priority clinical quality targets: lipid management and diabetic glucose control as well as to KPNW's drug cost initiatives. The MMP began with lipid management as the initial quality target. MMP measured and managed lipids for 31% of KPNW's members at highest risk for cardiovascular (CV) problems and by 1999 was managing 38% of highest-risk lipid patients. In Fall 1998, the MMP added responsibility for drug cost initiatives and for a second Regional quality target, management of glycemic control in patients not responding to newer oral drug therapies for diabetes mellitus. KPNW has an established record of improving glycemic control in the diabetes mellitus population, but more than 50% of diabetes patients who were prescribed newer oral agents were not achieving the benefits of good glycemic control. The MMP added this population that was failing to respond as a high priority when responsibilities expanded to diabetes drug therapy management. The MMP also began work with eldercare high-risk drug therapies and additional drug cost initiatives, developed a multidisciplinary model with nursing, and added initiation of aspirin therapy by protocol as one of the most important therapies to reduce cardiovascular risk (Table 2). Competency-based training assured that pharmacists and nurse care managers initiated aspirin therapy according to established protocols. Methodology Under the old model, a majority of clinical pharmacy resources was allocated to low-risk primary patients. To improve the health outcomes of our population, MMP needed to increase the percentage of high-risk CV members managed. In early 1998, the MMP initiated population-based care with outreach to the highest-risk CV population. High-risk patients were either referred to the MMP by physicians or harvested from one of two sources--a newly defined hospital discharge list or the newly developed disease state "high-risk" list. Standardized processes were developed by MMP personnel to improve patient care efficiency, documentation, and communications. Each patient's history is assessed, and an individualized care plan is developed according to established clinical practice guidelines. Pharmacists initiate therapy, monitor patients, and help patients to achieve their goal. Once patients reach a goal, they are categorized for maintenance monitoring. In an integrated multidisciplinary model recently added to MMP pharmacy care, nurse care managers work collaboratively to assist patients with paneling, conduct smoking assessments, and suggest educational opportunities. The MMP launched each priority quality and cost initiative through electronic communications from clinician leadership and inservice presentations with clinicians and location pharmacy staff. Presentations included over 200 clinician and health care team meetings (which reached approximately 500 clinicians, 200 nurses, 90 managers, and 250 other health care team personnel), and 90 pharmacy inservice sessions, which reached 400 pharmacy staff. MMP pharmacists also made more than 1000 one-to-one clinician-pharmacist contacts to provide academic detailing on the top three drug cost initiatives. Pharmacists, support personnel, and nurse care managers working with the MMP focus on the health of the entire population as they serve the individual. Through the MMP, the KPNW Regional Pharmacy Department broke new ground in partnering with physicians, local health care teams, and patients to find better ways to manage drug therapies and thus improve health outcomes. High-quality people and a positive team environment of continuous quality improvement are credited for improved patient care outcomes and improved workload and cost efficiencies. Results Quality/Member
Impact LDL measurement improved from 61.4% in the first quarter of 1998 to 69.2% in the fourth quarter of 1998. In 1999, the population at CV risk was defined to more closely align with the HEDIS measures. This reclassification resulted in reducing the size of the population to include patients aged 75 years and under. With this new population, LDL measurement was 73.5% in the first quarter of 1999 and increased to 84.2% by the fourth quarter of 1999. LDL management to 130 mg/dL improved in 1999: from 67.4% in the first quarter of 1999 to 72.1% by the fourth quarter of 1999. In addition, LDL management to 100 mg/dL improved: from 39.3% in the first quarter of 1999 to 43.7% by the fourth quarter of 1999 (Figure 4). Regional compliance with clinical practice guidelines improved with a shift of MMP resources focused on high-risk secondary-prevention patients. In 1997 and early 1998, clinical pharmacy resources with work prioritized in response to the daily demand from physicians seeing patients coming into the medical office had focused primarily on low-risk primary-prevention patients. A change to population-based care with the MMP improved the priorities of clinical pharmacy services from 31% high-risk secondary-prevention patients and 69% low-risk primary-prevention patients to 87% secondary-prevention patients and 13% primary-prevention. Implementation of staff-identified improved efficiencies allowed the MMP to systematically triple the number of high-risk patients managed from fewer than 2000 in early 1998 to nearly 6000 by yearend 1999 (Figure 5). A comparison of Northwest Region high-risk patients managed by MMP compared with non-MMP (those not managed by MMP) evaluated LDL measurement, LDL management, biomathematical estimates of ten-year myocardial infarction rates, and increase in life-years. Of secondary-prevention patients managed by the MMP, 99.1% had LDL measured as of 6/30/99, when the evaluation was conducted. Of secondary-prevention patients managed by the MMP, 91% achieved LDL of < 130 mg/dL compared with 67.6% in those not managed by the MMP. In the same patients, 68% managed by MMP achieved LDL of < 100 mg/dL compared with 45.4% in those not managed by the MMP (Figure 6). Biomathematical modeling of MMP lipid management care compared with the traditional model (non-MMP) estimates a decrease in myocardial infarction (MI) (92 ± 50) and an increase in life-years (90 ± 50) in ten years as a direct result of MMP management (Figure 7). The model also shows that improvement in these health care outcomes becomes evident as early as two years after management by MMP. During the third quarter of 1999, glycemic control became the second quality priority added to MMP responsibilities. The MMP focused on patients prescribed newer oral therapies who had failed to respond. A preliminary evaluation, when number of patients included was still quite small (MMP-managed = 4% and non-MMP-managed = 96% of general diabetes mellitus patients), suggested greater improvement in MMP-managed vs non-MMP-managed patients. Patients who had previously failed to respond to newer agents for glycemic control who were later managed by the MMP showed 18% greater improvement than the non-MMP-managed general diabetes mellitus population. Eighty-four percent of MMP patients achieved goal of HBA1c 8 mg/dL vs 63% of non-MMP-managed patients (Figure 8). Mean improvement in HBA1c was also higher for MMP patients than for non-MMP patients (decrease of 0.84 mg/dL vs decrease of 0.63 mg/dL). Results of mailed patient satisfaction surveys returned from 309 (40%) of 774 of members who achieved LDL goal in the first nine months of 1999 indicated that 96% were extremely satisfied or very satisfied with the care provided by MMP. In addition, as current KPNW members, 97% indicated they would definitely or probably recommend the MMP program to family members or friends (Figure 9). Responding members consistently expressed appreciation for KPNW's caring attitude and proactive outreach. Results of satisfaction surveys returned from 161 of 202 (79.7%) clinicians surveyed indicated that: 96% agree or strongly agree that MMP pharmacists are an important part of the local health care team; 97% agree or strongly agree that MMP pharmacists play an important role in achieving clinical targets; 100% believe the MMP provides excellent or good quality of care; and 95.7% agree or strongly agree that patients are satisfied with the care provided by MMP (Figure 10). Clinicians appreciated the time savings, consistent processes, and high quality of care that the MMP provides. Cost
Impact The cost of drug therapies to lower cardiovascular morbidity and mortality has increased as a result of the MMP focus to improve clinical quality. This cost investment is balanced with biomathematical modeling that predicts improved health outcomes for MMP patients compared with non-MMP patients. These improvements would become evident within two years and include estimates of a decrease in MI of 92 (± 50) and an increase in life-years of 90 (± 50) in ten years as a direct result of MMP management of lipids to improve clinical quality (Figure 7). In today's health care environment, it is often a challenge to invest scarce resources in improvements which do not have short-term returns. The MMP balanced priorities between improved utilization, which had short-term drug cost reductions, and improvement in clinical quality, which will provide longer-term returns with improved health outcomes. Direct
Patient Care Impact The MMP model resulted in staff and process changes to apportion resources to the highest-risk population by:
In addition, the MMP enhanced the services provided to patients by:
Patients are highly satisfied with the proactive communication and ongoing availability of MMP staff to answer questions via local and toll-free telephone numbers. Patients understand that a team of experts manages their care, individualized to their specific drug therapy needs, in collaboration with their clinicians. Patients appreciate the positive recognition they receive when they achieve their therapeutic goals and are comforted that the MMP continues to stay in contact through maintenance follow-up (Figure 9). Innovation/Leadership In the new model, MMP personnel take an active role in communicating with internal and external customers. Communication tools to define MMP services and changes are centrally developed. MMP pharmacists use the tools at local health care team meetings to facilitate discussion about the clinical targets or drug initiatives. In addition, the MMP uses satisfaction surveys to obtain ongoing feedback regarding MMP services, quality of care, and opportunities for improvement. Another innovation in the MMP model is designing processes to address varying needs of individual patients as their health care needs evolve. MMP population-based processes and resource allocation are designed to individualize care to meet the continuum of needs of the individual. Resources are increased or decreased depending on patient need. This flexibility supports most efficient use of resources. The individualized care for a patient not at goal is different from the level of care for a patient who has achieved goal and is in maintenance. The care for a patient who may be experiencing an adverse drug event is different than the level of care for a patient who tolerates the same medication without adverse effects. In addition, the most appropriate type of patient interaction is also considered, ie, reminder letter, personal phone call, group appointment, or other appropriate interaction. Appropriate level of care is routinely considered in deciding on the best-qualified and least-costly process or personnel to employ. The MMP makes ongoing improvements; this work environment requires that all personnel participate and function comfortably in an environment of continuous change and improvement. Summary
and Conclusions The MMP process is shaping state and national pharmaceutical care delivery models. KPNW has been asked to discuss the MMP at:
Now that the KPNW culture has changed, the MMP will move forward by continuing to extend its scope of care beyond lipid management, glycemic control in selected diabetes mellitus therapies, and aspirin therapy. Focus will expand to improving outcomes and reducing costs of other drug therapies. The infrastructure is in place to continuously improve processes and further expand collaboration with clinicians, staff, and administrators to meet changing clinical and cost priorities. KPNW's experience shows that the MMP is a transferable model that can assist other integrated health systems in providing high-quality, cost-effective clinical pharmacy services to a large population.
References 1. Kaiser Permanente Interregional President's Quality Improvement Best Practices Recommendations for Clinical Pharmacy Services, 1997. 2. Lee NL. Implementing Challenges from the ASHP Conference "Pharmacy in Managed Care: Vision for the Future": Prioritization and Implementation of Challenges; Pharmaceutical Care in Managed Care Pharmacy. Special Session of American Society of Health System Pharmacists Meeting, Las Vegas, NV, December, 1998. 3. Wright TL. Population-based medication management of CV risk: Dyslipidemias, Oregon Society of Health System Pharmacists Annual Meeting, Skamania, Washington, May, 1999. 4. Ashley R, Boschee G, Grant M, Johnson V, Perry P, Ramage J, et al. Improving the health of populations: An integrated Medication Management Program, Oregon Society of Health System Pharmacists Annual Meeting, Skamania, Washington, May, 1999.
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