RESUMO
OBJECTIVE: To review the literature on the subject of quality improvement principles and methods applied to pharmacy services and to describe a framework for current and future efforts in pharmacy services quality improvement and effective drug therapy management. BACKGROUND: The Academy of Managed Care Pharmacy produced the Catalog of Pharmacy Quality Indicators in 1997, followed by the Summary of National Pharmacy Quality Measures in February 1999. In April 2002, AMCP introduced Pharmacy's Framework for Drug Therapy Management in the 21st Century. The Framework documents include a self-assessment tool that details more than 250 specific "components" that describe tasks, behaviors, skills, functions, duties, and responsibilities that contribute to meeting customer expectations for effective drug therapy management. FINDINGS: There are many opportunities for quality improvement in clinical, service, and cost outcomes related to drug therapy management. These may include patient safety; incidence of medical errors; adverse drug events; patient adherence to therapy; attainment of target goals of blood pressure, glucose, and lipid levels; risk reduction for adverse cardiac events and osteoporotic-related fractures; patient satisfaction; risk of hospitalization or mortality; and cost of care. Health care practitioners can measure improvements in health care quality in several ways including (a) a better patient outcome at the same cost, (b) the same patient outcome at lower cost, (c) a better patient outcome at lower cost, or (d) a significantly better patient outcome at moderately higher cost. Measurement makes effective management possible. A framework of component factors (e.g., tasks) is necessary to facilitate changes in the key processes and critical factors that will help individual practitioners and health care systems meet customer expectations in regard to drug therapy, thus improving these outcomes. CONCLUSIONS: Quality improvement in health care services in the United States will be made in incremental changes that rely on a structure-process-outcome model. The structure is provided by evidence created from controlled randomized trials and other studies of care and system outcomes that are based on the scientific method. The process portion is created by the application of evidence in the form of clinical practice guidelines, clinical practice models, and self-assessment tools such as Pharmacy's Framework for Drug Therapy Management. Incremental changes in structure and process will result in the desirable outcome of meeting customer needs for more effective drug therapy and disease management. DISCLOSURES: Authors Richard N. Fry and Steven G. Avey are employed by the Foundation for Managed Care Pharmacy, a nonprofit charitable trust that serves as the educational and philanthropic arm of the Academy of Managed Care Pharmacy; author Frederic R. Curtiss performed the majority of work associated with this manuscript prior to becoming editor-in-chief of the Journal of Managed Care Pharmacy. This manuscript underwent blinded peer review and was subject to the same standards as every article published in JMCP.
Assuntos
Satisfação do Paciente , Assistência Farmacêutica/normas , Farmacêuticos/normas , Papel Profissional , Melhoria de Qualidade/normas , Qualidade da Assistência à Saúde/normas , Humanos , Programas de Assistência Gerenciada/normas , Programas de Assistência Gerenciada/tendências , Erros de Medicação/prevenção & controle , Erros de Medicação/tendências , Reconciliação de Medicamentos/normas , Reconciliação de Medicamentos/tendências , Assistência Farmacêutica/tendências , Farmacêuticos/tendências , Melhoria de Qualidade/tendências , Qualidade da Assistência à Saúde/tendênciasAssuntos
Custo Compartilhado de Seguro , Custos de Medicamentos , Seguro de Serviços Farmacêuticos , Legislação de Medicamentos , Adesão à Medicação , Política , Medicamentos sob Prescrição/economia , Medicamentos Genéricos/administração & dosagem , Medicamentos Genéricos/economia , Medicamentos Genéricos/uso terapêutico , Prática Clínica Baseada em Evidências , Humanos , Patient Protection and Affordable Care Act , Medicamentos sob Prescrição/administração & dosagem , Medicamentos sob Prescrição/uso terapêutico , Estados UnidosRESUMO
Popular press coverage of the Medicare Part D coverage gap is based largely on research conducted using retrospective analyses of administrative claims data. These datasets are incomplete because they lack information about methods of obtaining medication that are commonly used by seniors, including free samples, generic drug discount programs, over-the-counter substitution, and patient assistance programs. As a result, evidence about the effects of 100% cost sharing on seniors is limited and suboptimal. Although the current deficit of information about the coverage gap is not entirely unexpected because the Medicare Part D program is relatively new, reliance on claims-based analyses to inform questions that claims data cannot possibly address accurately has tended to mislead and politicize rather than produce constructive policy guidance. Numerous important health policy questions remain unaddressed. These questions are becoming especially important as optimal approaches to providing health care to seniors are the subject of an increasingly vigorous debate.
Assuntos
Envelhecimento/psicologia , Custo Compartilhado de Seguro/economia , Custos de Medicamentos , Conhecimentos, Atitudes e Prática em Saúde , Seguro de Saúde (Situações Limítrofes)/economia , Medicare Part D/economia , Adesão à Medicação , Medicamentos sob Prescrição/economia , Fatores Etários , Redução de Custos , Medicamentos Genéricos/economia , Medicina Baseada em Evidências , Acessibilidade aos Serviços de Saúde/economia , Humanos , Seguro de Serviços Farmacêuticos/economia , Projetos de Pesquisa , Estados UnidosAssuntos
Reforma dos Serviços de Saúde/economia , Política de Saúde/economia , Seguro Saúde/organização & administração , Projetos de Pesquisa , Serviços de Saúde/economia , Humanos , Seguro Saúde/economia , Seguro Saúde/ética , Pesquisa/normas , Estados Unidos , United States Agency for Healthcare Research and QualityAssuntos
Legislação de Medicamentos/tendências , Uso Off-Label/legislação & jurisprudência , Medicamentos sob Prescrição , Anticorpos Monoclonais/uso terapêutico , Anticorpos Monoclonais Humanizados , Antineoplásicos/uso terapêutico , Antipsicóticos/efeitos adversos , Antipsicóticos/uso terapêutico , Bevacizumab , Neoplasias da Mama/tratamento farmacológico , Dibenzotiazepinas/efeitos adversos , Dibenzotiazepinas/uso terapêutico , Custos de Medicamentos , Rotulagem de Medicamentos , Acessibilidade aos Serviços de Saúde , Reembolso de Seguro de Saúde , Midodrina/efeitos adversos , Midodrina/uso terapêutico , Medicamentos sob Prescrição/economia , Fumarato de Quetiapina , Estados Unidos , Vasoconstritores/efeitos adversos , Vasoconstritores/uso terapêuticoRESUMO
An article on the front page of the Wall Street Journal on October 6, 2006, thrust into the public media the otherwise esoteric controversy concerning the use of average wholesale price (AWP) as the primary basis for reimbursements to pharmacies for pharmaceuticals in the United States. Although used widely for nearly 40 years, AWP had been criticized prior to this investigative report as unreliable, subject to manipulation, and not representative of the actual purchase price for pharmaceuticals. The Wall Street Journal article, based on a tentative settlement of litigation in which First DataBank (San Francisco, CA) and the McKesson Corporation (San Francisco, CA) were accused of unilaterally increasing AWPs, included the findings that (a) at least since 2003, AWP was not based on calculation of an "average" wholesale price but instead reflected the pricing of McKesson Corporation, a single drug wholesaler; and (b) AWP had undergone a systematic change beginning in 2001 when First DataBank had converted its markups of wholesale acquisition cost (WAC) to a common multiplier of 1.25,1 effectively increasing the AWP by 4% for AWPs that were previously calculated using a multiplier of 1.20. In March 2009, the future of AWP became uncertain as a result of circumstances surrounding the court settlement of the litigation that had begun in 2005 against First DataBank. On March 17, 2009, U.S. District Court Judge Patti B. Saris approved the proposed settlement of 2 civil action lawsuits filed by private health plan payers of pharmaceuticals against the 2 largest publishers of AWP, First DataBank (along with wholesaler McKesson) and Medi-Span (Indianapolis, IN, subsidiary of Wolters Kluwer Health). On March 30, 2009, Judge Saris signed a final order and judgment certifying the class (of "Private Payor" purchasers) which settled 2 national class action lawsuits against the 2 largest publishers of AWP. As part of the formal settlement, Medi-Span and First DataBank agreed to adjust the markup factor used to calculate AWP downward to 1.20 times WAC "for any prescription pharmaceutical" that had "a mark up factor basis from WAC to AWP in excess of 1.20" for the 1,442 specific national drug code (NDC) numbers that were listed in the court complaint. The "rollback" of AWP as a result of reducing the WAC/DP (direct price) multiplier to no more than 1.20 was implemented by First DataBank and Medi-Span on September 26, 2009, 180 days from the date of the judgment, as ordered. At the same time, these AWP publishers voluntarily implemented price modifications to all products that had a WAC markup greater than 1.20. This decision expanded the list of NDC numbers from the 1,442 specified in the lawsuit to well over 50,000 items. The expanded list included both prescription and nonprescription (over-the-counter [OTC]) items, both active and inactive NDC numbers on the drug database, as well as a variety of markup factors. The adjusted AWPs had markup factors that ranged from 1.20 to 1.33. About two-thirds to three-fourths of the NDC numbers with adjusted AWPs had a pre-settlement WAC markup of 1.25. This U.S. District Court decision on March 30, 2009, was also accompanied by separate announcements from the defendants Medi-Span and First DataBank that they would voluntarily discontinue publication of AWP.