Cost Containment Strategies
Research has suggested the hazards and ethical problems in the overuse of services in fee‐for‐service settings (where payment is made based on service rendered to individuals for individual services) rather than service underuse in capitated care (where payment is made based on service rendered to a group of patients) (Berwick 1994; Leape et al., 1990). Over the years, cost containment strategies have targeted the financing and reimbursement sides of health care. Financing strategies have used health services regulation and limitation by means of taxes or insurance premiums and encouraged competition such as managed competition. Reimbursement containment strategies have used regulatory and competitive price controls and utilization controls, such as capitation, patient cost sharing, and utilization management. Capitation and prospective payment have had some of the most significant impacts on cost containment.
Even though legislation creating managed care was passed in 1973 (the Health Maintenance Organization Act), managed care did not become a major player or driving force in health care until the late 1980s. In an effort to reduce the number of hospitalizations and control profit incentives for health care providers, managed care plans offered hospitals and practitioners a capitated set fee for office visits and hospitalizations for a group of patients. Capitation is the payment of a fixed dollar amount, per person, for the provision of health services to a patient population for a specified period of time, for example, 1 year. Under capitation, health care organizations benefit from using their financial resources to keep people well. Otherwise, health care providers bear the financial loss. Then in the mid‐1990s, the U.S. population had quality concerns with this system and backlashed against managed care organizations.
Reacting to rapidly increasing costs to Medicare, the Tax Equity and Fiscal Responsibility Act(TEFRA) passed in 1982 mandated the Prospective Payment System(PPS) to control health care costs. For Medicare Part A services, PPS uses Medicare's administrative data to develop and continually refine PPS payments based on diagnosis‐related groups (DRGs), that is, patients with similar diagnoses. The PPS is a method of reimbursement in which Medicare payment is made based on a predetermined, fixed amount for reimbursement to acute inpatient hospitals, home health agencies, hospices, hospital outpatient and inpatient psychiatric facilities, inpatient rehabilitation facilities, long‐term care hospitals, and skilled nursing facilities. For Medicare Part B services, the Resource‐Based Relative Value Scale(RBRVS) is used to determine reimbursement amounts for practitioner services. The major problem that the CMS has encountered with funding prospective payment is DRG creep, in which health care providers up code or over bill a patient to indicate a need for financial reimbursement for more expensive health care services to recoup what the health care provider believes is a more equitable payment.
The health care report To Err Is Human, confronted health care clinicians and managers with concerns about the poor quality of health care attributable to misuse, overuse, and underuse of resources and procedures, which was responsible for thousands of deaths (IOM, 1999). The health care report, Crossing the Quality Chasm (IOM, 2001), and several large studies (McGlynn et al., 2003; Thomas et al., 2000), have shown that the quality of health care in the United States is at an unexpected low level and needs improvement in many dimensions, given the amount of money the United States spends on health care ( Table 2.7). One implication is that if a measure is described in a way that is clear and understandable, people are more likely to value the measure (AHRQ, 2011).
Table 2.7 Health Care Dimensions Needing Improvement
Health Care Should Be |
Health Care Should |
1. Safe: Avoid injuries from care intended to help patients. |
1. Offer care based on continuous healing relationships: Make care available every day through face‐to‐face visits, telephone, Internet, and other means. |
2. Effective: Provide services based on scientific knowledge to all who could benefit, and refrain from providing services to those not likely to benefit (avoid overuse and underuse). |
2. Customize care based on patient needs and values: Provide care responsive to patient needs and preferences. |
3. Patient centered: Provide respectful and responsive care to individuals; patient preferences, needs, and values must guide clinical decision making. |
3. Have the patient as source of control: Foster patient empowerment and autonomy through information and shared decision making. |
4. Timely: Reduce wait time and harmful delays for those who receive and give care. |
4. Share knowledge and free flow of information: Facilitate patient access to his or her own medical information and to available clinical knowledge. |
5. Efficient: Avoid waste, for example, of equipment, supplies, ideas, energy, and other costly resources. |
5. Use evidence‐based decision making: Provide consistent quality of care based on best available scientific knowledge. |
6. Equitable: Provide care consistent in quality irrespective of gender, ethnicity, geographical, and socioeconomic factors. |
6. Develop safety as a systems property: Develop systems of safety that mitigate error, promote patient safety, and reduce risk of injury. |
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7. Be transparent: Make information available to patients and families about health plans, hospitals, clinical practice, and alternative treatment options, including performance related to their safety, evidence‐based practice, and patient satisfaction. |
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8. Anticipate needs: Anticipate patient needs rather than respond to events. |
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9. Continuously decrease waste: Use limited resources wisely. |
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10. Cooperate among clinicians: Collaborate and coordinate care between clinicians and institutions. |
Source: Compiled with information from the Institute of Medicine. (2001). Crossing the quality chasm: A new health system for the 21st century . Washington, DC: National Academy Press; and Berwick, D. M. (2002). A user's manual for the IOM's ‘Quality Chasm’ report. Health Affairs, 2 (3), 80–90.
Groundbreaking research beginning in the 1970s and continuing into the 1990s demonstrated that there was significant variation in utilization of specific health care services associated with geographical location, provider preferences and training, type of health insurance, and patient‐specific factors such as age and gender (Adams, Fraser, & Abrams, 1973; Greenfield et al., 1992; Leape, 1992; Safran, Rogers, Tarlov, McHorney, & Ware Jr., 1997; Wennberg & Gittelsohn, 1973). Associations between utilization rates of health care services have been found with availability of services and technologies, for example, MRIs, hospital beds, practitioners (Joines, Hertz‐Picciotto, Carey, Gesler, & Suchindran, 2003), prevalence and severity of morbidities (Dunn, Lyman, & Marx, 2005; AHRQ, 2008b), race or ethnicity (AHRQ, 2008b), patient adherence, health‐seeking behaviors of patients (Calvocoressi et al., 2004), and many other factors. Variation in the delivery and quality of health services is also associated with socio‐demographics, hospital types (e.g., urban and rural, teaching and nonteaching), and clinical areas (e.g., heart disease, diabetes, pneumonia, and clinical preventive services). Regions of the country and health care providers with more resources had higher rates of use and cost. Efforts to decrease the variation of health care practices through standardization of care with quality, evidence‐based guidelines are important to improve clinical decision making, care delivery, health outcomes, and cost efficiency.
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