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. 1993 Winter;15(2):173–202.

Social/Health Maintenance Organization and Fee-for-Service Health Outcomes Over Time

Kenneth G Manton, Robert Newcomer, Gene R Lowrimore, James C Vertrees, Charlene Harrington
PMCID: PMC4193417  PMID: 10135342

Abstract

Evaluating the performance of long-term care (LTC) demonstrations requires longitudinal assessment of multiple outcomes where selective mortality and disenrollment, if not accounted for, can give the appearance of reduced (or enhanced) efficacy. We assessed outcomes in social/health maintenance organizations (S/HMOs) and Medicare fee-for-service (FFS) care using a multivariate model to estimate active life expectancy (ALE). S/HMO enrollees and samples of FFS clients in four sites were analyzed and outcome differences assessed for a 3-year period. Results provide insights into S/HMO performance under different conditions and, more generally, into evaluating LTC demonstrations without randomized client and control groups.

Introduction

The utility of LTC for functionally impaired, community dwelling elderly is well documented. In-home services (for meal preparation, shopping, laundry, grooming, and dressing) and out-of-home services (such as adult day care, recreational, physical, and occupational therapy) improve client and caregiver lives (e.g., Kemper, 1988). The value of case management (i.e., needs assessment, care planning, coordinating and monitoring of services) is also evident. Though improving client and caregiver outcomes, however, these services do not appear to reduce costs—possibly due to methodological factors (e.g., defining their cost effectiveness relative to institutional care) (Kemper, 1988; Weissert, Cready, and Pawelak, 1988; Zawadski, 1984). Institutional costs are limited by State Medicaid programs and may be insufficient to bring about therapeutic innovations or to prevent quality-of-care problems (e.g., decubitus ulcer, malnutrition, pneumonia, or urinary tract infection [UTI]) (Brandeis et al. 1990; Braun, 1991; Dontas et al., 1991; Fiatarone et al. 1990; Gloth et al., 1991; Gross, 1988; Pinchcofsky-Devin and Kaminski, 1987).

Consequently, an alternative model for delivering LTC to community populations, the S/HMO, was developed. It was hoped that LTC, provided in a capitated system (as it is in a S/HMO), might improve cost effectiveness and outcomes. A Health Care Financing Administration (HCFA) demonstration of S/HMOs started in January 1985. S/HMOs were to:

  • Provide hospital, physician, home health, extended benefit (e.g., eye glasses, hearing aids, drugs) and LTC services (e.g., nursing home, home-maker, and transport) to voluntarily enrolled clients paying a monthly premium.

  • Use case managers to determine eligibility for, and select, LTC services. Access is limited by disability criteria and coverage limits.

  • Serve both impaired and unimpaired elderly to maintain health and function.

  • Be reimbursed by capitation payments from pooled Medicare, Medicaid (for eligible enrollees), and member premiums. S/HMOs assumed risk for all costs after 30 months. Integrated funding and financial risk are incentives for cost control and service flexibility (Leutz et al.,1985).

Some S/HMO features complicate the evaluation process. Because enrollment is voluntary, and marketability important, persons with specific health attributes can self-select into S/HMOs. Thus, a randomized study design could not be used. Statistical controls for health differences between S/HMO enrollees and members of comparison FFS samples are necessary. Additionally, the LTC provided by S/HMOs is available to persons in FFS. That is, the intervention depends on the degree to which S/HMOs make LTC accessible and not on its presence or absence. Variation in interventions makes comparisons of S/HMO and FFS outcomes complex. Here we focus on one outcome—the effect of being in a S/HMO on a person's functioning, relative to being in Medicare FFS, controlling for initial health and mortality. In this analysis we do not deal with cost issues, as they are treated in other reports.

Comparing outcomes longitudinally between S/HMO enrollees and FFS samples is difficult because of systematic health changes, mortality, and sample loss. For example, in the National Long-Term Care Channeling demonstration, the effect of increased access to case management (both with and without payments for additional services) was evaluated in 10 sites during an 18-month period. Persons with impairments were selected for the study and randomized into one of four groups (i.e., case and control groups defined for two interventions). Differences were found on baseline interviews in case and control response rates (10 percent higher for cases), response times (cases responded 5.4 days faster), and willingness (cases, on average, required 29 percent fewer contacts). Timing was important in assessing hospitalized or institutionalized persons (Brown and Mossel, 1984).

In S/HMOs, the content of interventions (i.e., services offered) also changes with time. LTC demonstrations are often designed as if impairments are progressive with little potential for improvement. LTC is viewed as “palliative.” Analyses of national longitudinal surveys, however, show that many elderly, frail persons regain function (Manton, Corder, and Stallard, 1993; Suzman et al., 1992). Thus, outcomes involve improvements as well as decrements in function. Finally, for the elderly, impairment is a matter of degree. At 85 years of age, most persons may have an activities of daily living (ADL) or instrumental activities of daily living (IADL) dysfunction, though the proportion losing social autonomy, i.e., those who are wholly incapable of performing any self-care, is small (Manton et al., to be published). Assessments cannot simply be made of transitions into or out of discrete impairment states. The degree of impairment on multiple dimensions (e.g., mobility versus cognitive functioning versus manual dexterity) must be assessed to compare outcomes of different care delivery systems over time. In this article, we examine whether the integration of acute and LTC services offered by the S/HMOs produced higher ALEs—periods free of impairment (Katz et al., 1983) —than for persons receiving customary and usual Medicare FFS care, controlling for differences in health at enrollment.

Prior Studies of HMOS

Except for the 1985 HCFA S/HMO demonstrations, there have been no prior S/HMO demonstrations. There are multiple studies of the care of elderly persons in capitated health systems (i.e., HMOs) that do not provide LTC. The following criteria have been used to assess HMO outcomes.

Most studies of Medicare HMOs examine enrollment and attrition. Riley, Rabey, and Kasper (1989) compared mortality rates for 3 HMOs with FFS for 6 years following enrollment, controlling for age, gender, and Medicaid and institutional status. HMO mortality was lower in the first year, implying favorable selection. Mortality increased to FFS levels by the second year in two plans. The third approached FFS levels over 5 years due to favorable attrition, i.e., mortality 2 years after disenrollment was higher than for continuing members. Two other studies found HMO mortality rates lower than FFS mortality rates. One examined mortality for 2 years following enrollment (U.S. General Accounting Office, 1986). In the other study, mortality in an Oregon HMO was compared with State mortality rates over 6 years—adjusted for age, gender, and smoking or non-smoking status (McFarland et al., 1986). These studies did not control for functional status. Therefore, mortality findings are ambiguous because they can be interpreted as either an indirect cost measure (i.e., high terminal care costs) or a health measure.

In the Medicare competition evaluation, the service use of HMO and FFS clients were compared for 2 years pre-enrollment and mortality rates were compared for 2 years post-enrollment. Prior use was lower in 13 of 14 HMOs; mortality lower in 12 of 17 HMOs; both results suggest favorable selection for HMOs. Disabled persons disenrolled from HMOs at higher rates (Brown, 1988). In addition, quality of care was assessed (Langwell and Hadley, 1989). Care access (controlled for self-reported symptoms) was measured by whether a health professional was seen, and baseline and followup health status were compared for all clients. No significant differences were found between HMOs and FFS regarding care access or health change. HMO records were more complete, and contained more reports on tests and immunizations. There were few differences in drugs prescribed, history taking, or exams for those with congestive heart failure. Some practice patterns varied (e.g., HMO physicians hospitalized unstable angina cases more often). Though an improvement over assessing mortality differences, the quality of care indexes are partly confounded with service use. None of the HMO studies examined functional change as an outcome.

Case Selection

Our analysis included all enrol lees in 4 S/HMOs (n = 10,838) in June 1986 (in Long Beach, California and Portland, Oregon) or December 1986 (in Brooklyn, New York and Minneapolis, Minnesota), and samples (n = 16,664) of non-institutionalized Medicare FFS clients 65 years of age or over living in those 4 areas. FFS clients enrolling in HMOs during the study were followed. This HMO group of clients (i.e., persons self-selected after 1986) differs from 3 HMO samples of 1,000 persons each enrolling in HMOs from Medicare FFS in 1985 and 1986. Data collected on the HMO samples included a health screening form (HSF), prior costs (Manton et al., 1994), reasons for enrollment (Newcomer, Harrington, and Friedlob, 1990), and mortality and disenrollment (Manton et al., unpublished), but did not include health changes or post-enrollment service use. Those data were obtained for all members in the FFS samples—including persons entering HMOs during the study. Thus, the HMO samples were not analyzed, but FFS clients shifting to HMOs during the study were.

This evaluation is designed to assess the differences between S/HMOs and standard FFS care, and not those between S/HMOs and HMOs. During the demonstration, the benefits which distinguish S/HMOs from HMOs which provide extended care were reduced (Newcomer, Preston, and Harrington, 1991). Nonetheless, S/HMOs provide LTC services which are not reimbursed in extended care Medicare HMOs. Thus, changes in S/HMO benefits were not structural, but specific management decisions as service costs became clear. Data were collected to assess how S/HMO services changed relative to HMO services.

Persons applying to a S/HMO could be nursing home certifiable under State Medicaid criteria, but could not be in a nursing home. They may have previously been in a nursing home, or be considering entering a home. Consequently, nursing home residents are also out of scope for FFS samples. This exclusion's effect varies by age and gender. Nursing home residence is about 25 percent for persons 85 years of age or over, according to the 1985 National Nursing Home Survey (Hing, Sekscenski, and Strahan, 1989). Rates are higher for females and the oldest-old, and vary by health (e.g., about 45 percent of nursing home residents in 1985 had “dementia”). Thus, the exclusion differentially affects females, the very old, and persons with specific medical problems.

Response Rates and Biases

Non-response in the FFS sample can bias estimates of case-mix distributions. The FFS response rate for the HSF was 80.5 percent. The HSF response rate was 98.3 percent for S/HMOs because plans were required to screen persons before enrollment, though small numbers of enrollees initially received a comprehensive assessment form (CAF) if impairments were known to exist. Several persons died while applying. Thus, instead of defining S/HMO enrollees as only those with HSFs, persons were counted if they had received CAFs, had Medicare service use data, and were identified on Medicare records as a S/HMO enrollee.

Studies of health surveys (National Center for Health Statistics, 1966; Manton, Stallard, and Woodbury, 1991) find that elderly non-respondents are frailer and use more services than respondents. This is assessed in the evaluation by comparing the average costs of all Medicare-eligible persons in the catchment area to the average costs of FFS sample respondents. The average costs for the Medicare population (after institutionalized persons are removed) are 15 percent higher than those for sample respondents. Because Medicare costs are correlated with health and functional status, this suggests that FFS sample respondents are, on average, healthier and less impaired than the total Medicare population in each site (Manton et al., 1994). This bias should be against demonstrating favorable enrollment in S/HMOs. In addition, there is a “guaranteed” time bias in that terminally ill persons (those with an average of 3 months to live) are unlikely to change care providers, i.e., enroll in S/HMOs. To eliminate the comparable group from the FFS sample, we identified persons who died before the end of the interview period from Medicare records and divided them into two groups. FFS non-respondents dying before the median interview date (about 6 months; n = 765) in a site were excluded as terminal cases. Persons dying after that date are included and their characteristics imputed from the characteristics of respondents. This adjustment is most important for prior cost analyses (Manton et al., 1994). The vital status of all persons was determined from Medicare records. S/HMO and HMO enrollment and disenrollment dates were determined from group health membership files mapped to Medicare Automated Data Retrieval System files containing data on Medicare Part A and B service use.

Health Assessments

The initial assessment was a telephone-delivered HSF for the FFS sample and a self-completed mail-back HSF for S/HMO applicants. The HSF is based on the National Long-Term Care Survey (NLTCS) screening instrument (Durako, 1987). HSFs measure ADLs (e.g., toileting, dressing, bathing [Katz and Akpom, 1976]), IADLs (e.g., preparing meals, laundry, housework [Lawton and Brody, 1969]), and health conditions (e.g., diabetes, hypertension). Persons having two or more IADL (or one or more ADL) limitations received a CAF, administered by social workers or nurses to verify self-reported impairment.

FFS cases with no ADL and fewer than two IADL impairments were contacted annually by phone. S/HMO enrollees were contacted by mail-back questionnaires. S/HMO disenrollees were interviewed over the phone by evaluation staff. Persons reporting two or more IADL limitations at baseline or in the annual re-HSF were contacted semiannually. Those with two or more IADL, but no ADL, limitations were given a re-HSF. Those ever reporting an ADL impairment are given a re-CAF— usually by phone. CAFs were conducted for 3,234 (11.8 percent) of 27,482 FFS and S/HMO members. In 3 years, 8,506 CAFs were administered—an average of 2.63 extra contacts per interviewee. S/HMOs could identify health changes in clinical encounters. In FFS, clinical encounters did not trigger a CAF—the identification of health changes depended on a periodic, but complete, screening. In S/HMOs, screening after enrollment started about 6 months late and relied on mail-back instruments. Thus, it is less likely to be complete than the followup screening of FFS members by phone. CAFs may affect S/HMO service eligibility, which might cause bias toward recording less impairment (or more improvement).

Case-Mix Scores

Case-mix scores are calculated using grade of membership (GoM), a generalization of log linear (Bishop, Fienberg, and Holland, 1975) and latent class membership (LCM) (Lazarsfeld and Henry, 1968) analyses for categorical data. In log linear models, the membership of each person denoted by i in K independent groups is observed. That is, K group membership variables, gik (= 1 or 0), are observed, where gik describes whether individuals' observed characteristics relate to group Ks. For the K groups, cell probabilities for J-way tables, λkjl, are calculated from observed frequencies; thus, the λkjls define the groups. In LCM, group membership is not observed, so the probability of being in a group (Pˆik = Prob[gik = 1.0]) is estimated jointly with the λkjls. In GoM, not only is group membership unobserved, but persons may be “partial” members of groups. The giks in GoM representing partial membership are estimated such that kgik=1.0, and 0.0 ≤ gik ≤ 1.0, so that multiplying λkjls by giks reproduces the observed frequencies. Thus, GoM is used in this analysis to define a set of K case-mix classes from a series of health and functioning variables. The relation of person is health characteristics to the K classes is summarized in the K scores gik. The giks in GoM define within-group heterogeneity not represented in the LCM. The significance of this heterogeneity can be tested by determining if the GoM fits the data better because the models are parametrically nested.

GoM was applied to pooled HSF and CAF data so that giks could be updated for health changes. The updated scores (gikt) control for health variation, over individuals and time (t), in comparing S/HMO and FFS outcomes. In “pre-post” analyses, interventions are made at fixed times and do not describe systems with voluntary enrollment or disenrollment (such as S/HMOs) well, where interventions are of variable content, duration, and timing. Variables affecting choice interact with outcome—the decision to stay enrolled is made daily, and reflects the degree of satisfaction with services and outcomes.

In GoM, J multinomial variables for each of I persons (χij) are each coded as Lj binary (0, 1) variables, yijl. Continuous variables are divided into Lj intervals and then coded in binary form. The probability of yijl occurring is (site and coverage indexes suppressed),

p^ijlt=Prob(yijlt=1.0)=k(giktλkjl). (1)

Both the λkjl, and the gik are uniquely identified if J >2K (Woodbury, Manton, and Tolley, to be published), because selecting J variables determines the space, M, of all possible responses, yijl. The solution, B, is the intersection of the probability space, LB, defined by the pijlt estimated in equation 1, with the a priori determined M. Extreme points of B define the λkjl. The giks are the linear functions joining λkjls. The λkjl, are assumed time invariant; time is represented in gikt.

To assure gikts are comparable between FFS and S/HMO and over time, the K profiles (λkjl) are estimated from HSF and CAF data pooled over time, site, and coverage. The likelihood for the combined data is (+ indicates a index for which data is combined),

L=ΠiΠjΠlΠtΠcΠs(gikt++λkjl++)yijltcs, (2)

where measurement is at time t, c refers to coverage (e.g., S/HMO or FFS), and s to site (Manton et al., 1986; 1987). A person is given a CAF when a health change is detected in an annual re-HSF, semiannual monitoring of impaired persons, or in an S/HMO clinical visit. Because scores change at variable times, we divided each record into months (i.e., t = 1, 2, …, 36). If a CAF is administered at t +1, new gikt+1s are calculated if health changed. Otherwise the gikt are assumed constant. By using monthly histories we can estimate the time spent in specific health states (i.e., having specific gikt values). This deals with the variable assessment times, because how long a person remains in a case-mix class is decribed by the gikt.

The GoM likelihood in equation 2 (suppressing indexes for coverage, time, and site) is evaluated by iteratively solving two functions (Woodbury and Clive, 1974),

Lgik=1yi++i=1Il=1L2yijl(gikλkjlhgihλhjl) (3)

and

Lλkjl=i=1Iyijl(gikλkjl)hgihλhjli=1Il=1Ljyijl(gikλkjl)(hgihλhjl). (4)

Normally, terms in a likelihood for individuals are collected in an independent factor and only structural parameters (i.e., those not involving i) are estimated (Cox and Hinkley, 1974). To factor individual from structural parameters, assumptions are made about the distribution of individual parameters so that the information in structural parameters is restricted to a “small” number of data moments (e.g., the [J × (J+1)]/2 unique elements in a co-variance matrix for J variables in factor analysis). In equation 3, estimation of gik involves λkjl. In equation 4 estimation of λkjl involves gik. Thus, the sets of parameters are jointly estimated. This makes λkjl, estimates robust to individual variation because they are conditioned on the gik distribution. Estimates of giks do not have a prespecified distribution but produce unbiased estimates of up to the Jth order moments of the gik distribution (Woodbury, Manton, and Tolley, to be published). The λkjl estimates are consistent because equation 3 implicitly constrains the moments of the gik distribution across individuals.

To estimate parameters for external variables (for validation), or transition rates, two steps are needed. First, equations 3 and 4 are maximized for J health variables. Then, the parameters for the J variables in equations 3 and 4 are fixed to hold constant the definition of the K classes (i.e., λkjl) and individual scores (i.e., gik). Then equation 4 is maximized to produce conditional (on case mix) maximum likelihood estimation of λknl for the N added variables. Likelihood ratio tests can be formed to determine if external variables contain significant information not represented in case-mix groups. Mortality and coverage change probabilities may be estimated by defining transition variables for each case-mix group, i.e., λkN(l1l2) (l1 are time intervals, and l2 changes in status). Transition rates are estimated in a second maximum likelihood step again with the definition of case-mix groups fixed. The λkN(l1l2) describe discrete changes (e.g., death, coverage change) over 3 years of followup. They do not describe cohort changes.

Active Life Expectancy

The gikt and λkjl describe all information on health and mortality in 3 years of followup of an initially non-institutionalized population. They do not describe age-specific survival and disability changes for a cohort of such persons. This requires solving systems of difference equations for monthly intervals, to approximate life table differential (continuous time) equations. In those calculations, two additional equations are needed. The first describes health changes among survivors t to t +1:

gik(t+1)={Ageβkk}(gikt)+eik, (5)

where {Age • βkk} is a matrix of age-dependent transition rates between K case-mix groups. Four βkk matrices are estimated, one each for FFS and S/HMO males and females. The definition of gikts in equation 2 ensures their comparability over gender, coverage, and site (Manton, Woodbury, and Tolley, 1994).

The second describes mortality as an age-dependent quadratic function of the gikt,

μ(gikt)=(giktTQgikt){eθt}=(giktTQtgikt). (6)

In equation 6 all coefficients in Q are multiplied by eθt. θ is the percent per year of age increase in mortality. In equation 6, a person's risk changes as gikt changes according to equation 5. The performance of S/HMOs and FFS in maintaining function is described by βkk; and for survival by Qt. θ is the age-related, average effect of unobserved variables for FFS and S/HMO males and females. As information in gikt increases, θ → 0.0 (Manton et al., to be published).

Calculating cohort life tables requires using parameters in equations 5 and 6 to solve monthly difference equations. The proportion of a cohort, l, surviving to t +1, is,

lt+1=lt|l+VtQt|½exp{μt(g(t))+μt(g(t))22μt(g(t)+g(t)2)}, (7)

where g (t) is a vector of means of gikt and Vt their covariance matrix. Equations 8 and 9 show that g *(t) and (V*t) are functions of mortality (Qt) and case mix heterogeneity (Vt) or,

g(t)=(g(t)VtQtg(t))/kg(t)VtQtg(t)k (8)

and

Vt=(I+VtQt)1Vt. (9)

Mortality depends on ḡ(t) and Vt. Vt has deterministic (i.e., Age • βkk) and stochastic components. Diffusion increases, and mortality reduces, Vt. Diffusion must reflect the 0, 1 bounds on the gikts. We assume that Vt has, at most, Bernoulli variance, (gk(t+1)(1g(t+1)), and that correlations of gikts are constant from t to t +1. The correlation matrix R is estimated from Vt after conditioning on age. In the diagonal matrix, S, elements are square roots of the ratios of gikt variances to Bernoulli limits. S projects the gikt to a high dimensional spherical space so that, in computations, gikts are not “trapped” on “faces” of B. Wt+1 is a diagonal matrix with elements

g¯k(t+1)(1g¯k(t+1).

The new “constrained” variance is

Vt+1=Wt+1S R S Wt+1, (10)

which can be used to estimate a constrained diffusion matrix,

t+1=Vt+1CtVtC, (11)

where Ct = Age • βkk from equation 5. Changes in the means ( g (t)) of gikt for survivors are

g(t+1)=(Ageβ)g(t). (12)

Equations 7 through 12 are used to calculate cohort life tables for K case-mix groups. Cohort life tables differ from transition variables estimated in equation 2 because the 3-year experience of initially non-institutionalized persons of different ages is used to construct disability dynamics and mortality for the life of a cohort. Thus, there are three distinct sets of calculations. One generates the gikt, describing cases from the pooled data using equation 2. In those calculations we may estimate 3-year transition rates. Second, gikts are used to generate parameters for disability dynamics (in equation 5) and mortality (in equation 6). Those parameters are used in difference equations 7 through 12 to calculate cohort life tables. The individual components of cohort dynamics can be examined by fixing selected parameters in equations 7 through 12.

In a hazard model, the risk of an event is estimated for fixed covariates (Cupples et al., 1988). The difference equations use time-varying covariates. Thus, the difference equations produce insights about cohort dynamics that cannot be made using only a hazard function. The quadratic in equation 6, one component of the cohort calculations, is a hazard function. It is estimated by maximum likelihood and, because μ. (the mortality rate) is estimated directly, there are no problems of interpreting coefficients as in Cox or logistic functions (e.g., including quadratic terms in a Cox model makes the hazard scale dependent)—the function changes as risk factor levels change.

Results

To assess FFS or S/HMO outcomes, health variation over persons and time must be described. This requires defining multiple “Profiles” to characterize a person's health. The six profiles in Table 1 are described by comparing λkjls to the overall frequency of an attribute—e.g., 27.1 percent need help with meals. Someone who “fits” Profile 3,4, or 6 (i.e., has a high gik•t) requires assistance. Individuals matching Profiles 1,2, or 5 do not. The λkjl, can be discussed both as a profile of J attributes and as groups of cases characterized by a profile.

Table 1. Multivariate Values for 30 Health and Functioning Measures From Social/Health Maintenance Organization (S/HMO) Demonstrations: 1986-89.

Health and Functioning Measures Frequency Case-Mix Group

Healthy Acutely III Impaired Pulmonary Cardiac Frail

Percent
Functional Ability
Requires Assistance With:
1. Preparing Meals 27.1 0.0 0.0 100.0 100.0 0.0 100.0
2. Laundry 19.9 0.0 0.0 100.0 0.0 0.0 100.0
3. Light Housework 16.3 0.0 0.0 100.0 0.0 0.0 100.0
4. Grocery Shopping 15.8 0.0 0.0 100.0 0.0 0.0 100.0
5. Managing Money 21.2 0.0 0.0 100.0 42.1 0.0 100.0
6. Taking Medicine 14.8 0.0 0.0 100.0 0.0 0.0 100.0
7. Making Phone Calls 11.4 0.0 0.0 86.5 0.0 0.0 100.0
8. Eating 7.9 0.0 0.0 0.0 0.0 0.0 100.0
9. Getting In and Out of Chairs or Bed 22.2 0.0 0.0 0.0 100.0 0.0 100.0
10. Walking Around Inside 15.7 0.0 0.0 0.0 0.0 0.0 100.0
11. Driving or Using Public Transportation 32.3 0.0 0.0 100.0 100.0 0.0 89.2
12. Toileting 20.3 0.0 0.0 0.0 100.0 0.0 75.9
13. Dressing 16.2 0.0 0.0 0.0 100.0 0.0 100.0
14. Bathing 20.9 0.0 0.0 0.0 100.0 0.0 100.0
Individual:
15. Uses a Wheelchair or Walker 6.7 0.0 0.0 38.5 0.0 0.0 46.2
16. Uses a Cane 18.0 0.0 100.0 0.0 0.0 0.0 0.0
17. Is Bedfast 13.2 0.0 0.0 0.0 42.2 0.0 100.0
Medical Conditions
18. Diabetes Mellitus 17.6 100.0 100.0 100.0 0.0 100.0 0.0
19. Hypertension 31.7 27.6 100.0 29.7 0.0 100.0 0.0
20. Heart Trouble 18.6 0.0 0.0 0.0 0.0 100.0 0.0
21. Neurological Problems 11.2 0.0 100.0 0.0 0.0 0.0 40.8
22. Stroke 17.0 0.0 100.0 0.0 0.0 0.0 47.7
23. Lung or Breathing Problems 18.9 0.0 0.0 0.0 80.8 100.0 0.0
24. Chronic Cough 6.8 0.0 0.0 0.0 0.0 73.5 0.0
25. Cancer 16.3 0.0 100.0 0.0 49.8 0.0 10.0
26. Hardening of the Arteries 14.6 0.0 0.0 0.0 0.0 100.0 0.0
27. Stomach or Bowel Problems 20.9 0.0 100.0 0.0 0.0 100.0 38.6
28. Bladder Problems 15.5 0.0 0.0 0.0 44.4 100.0 0.0
29. Rheumatism or Arthritis 56.7 41.0 100.0 0.0 53.5 100.0 63.9
30. Other Health Problems 25.2 11.6 96.5 26.4 30.8 71.6 36.5
gk (weighted prevalence) 52.2 7.0 9.8 11.7 11.5 7.8

SOURCES: Data derived from health screening forms (HSFs) and comprehensive assessment forms (CAFs) administered by the authors. HSF data were collected from fee-for-service beneficiaries at baseline and from S/HMO enrollees upon application. Total HSF sample size is 27,503 cases. CAFs were completed semiannually by persons who identified functional disabilities on the HSF.

The profiles in Table 1 are defined by their association (λkjt) with health variables:

  • “Healthy”—Individual is unimpaired but has diabetes, hypertension, and joint disease. This profile is “healthy” relative to other case-mix groups.

  • “Acutely III”—Individual has cancer (100 percent), cardiopulmonary problems, and hypertension, but no impairment.

  • “Impaired”—Individual has IADL impairments suggesting early dementia but few other neurological problems. Medical conditions (e.g., diabetes) may be present.

  • “Pulmonary”—Individual has ADL impairments (42.2 percent bedfast), pulmonary problems (80.8 percent), and cancer (49.8 percent).

  • “Cardiac”—Individual is not impaired, but has multiple medical problems—including cardiopulmonary conditions (no stroke) and arteriosclerosis.

  • “Frail”—Individual is bedfast (100 percent) and limited on all ADLs and IADLs. Medical problems include stroke, cancer, neurological, stomach, and bowel problems. A person with a high score on this dimension, unless having excellent social and economic resources, would be at risk of institutionalization because he or she is 88.9 percent impaired on the 17 functional items. Thus, as the population ages, movement into the frail category serves as a measure of persons potentially needing institutionalization—because institutional residents were excluded at the study's start and are not represented in baseline health measures.

The predictive validity of the gik•t was examined on sociodemographics and service use (Reuben, Siu, and Kimpau, 1992). The λkNls describing these relations (calculated conditionally on case-mix scores) are presented in Table 2.

Table 2. Multivariate Values for Sociodemographic and Health Service Use Variables From Social/Health Maintenance Organization (S/HMO) Demonstrations: 1986-89.

Variables Frequency Case-Mix Group

Healthy Acutely III Impaired Pulmonary Cardiac Frail

Percent
Sociodemographic Variables
Gender:
Male 37.4 43.1 34.9 40.4 25.3 28.0 29.4
Female 62.6 57.0 65.1 59.7 74.7 72.0 70.6
Age:
64-69 Years 33.4 54.0 0.0 5.0 10.2 16.5 11.0
70-74 Years 22.1 22.8 0.0 66.1 11.5 14.7 10.0
75-79 Years 17.4 13.3 100.0 7.0 7.4 13.2 13.3
80-84 Years 14.2 7.6 0.0 9.4 55.5 12.6 16.8
85-89 Years 8.9 1.9 0.0 6.5 11.0 42.5 17.0
90 Years or More 4.0 0.5 0.0 6.1 4.5 0.5 31.9
Mean Age 75.3 71.7 77.5 75.8 80.5 80.1 83.2
Marital Status:
Married 51.3 58.7 12.5 43.9 36.0 41.1 55.7
Not Married 48.7 41.3 87.5 56.1 64.1 58.9 44.3
Living Arrangements:
Lives Alone 36.0 33.5 69.3 24.5 47.0 51.4 1.3
With Spouse 50.6 57.8 11.5 42.8 36.8 40.1 55.1
With Child 7.0 4.5 12.7 18.4 7.2 4.3 16.0
With Relative 3.4 2.7 5.4 5.6 5.1 1.7 6.0
With Unrelated Person 3.1 1.5 1.0 8.7 3.9 2.5 10.8
Type of Housing:
Group Care 1.4 0.3 0.0 6.4 4.5 0.1 4.4
Senior Housing 4.5 2.7 17.9 4.8 5.1 9.4 3.0
Other's Home 4.4 2.1 7.3 20.4 6.1 2.3 8.3
Own Home 88.5 93.8 72.1 67.0 83.7 86.4 82.1
Other 1.3 1.1 2.7 1.5 0.6 1.8 2.3
Self-Rated Health:
Excellent 23.4 36.8 0.0 10.4 11.5 0.1 7.5
Good 46.8 56.8 0.0 40.7 50.3 34.7 32.4
Fair 23.0 6.5 73.9 31.6 29.7 57.4 30.7
Poor 6.8 0.0 26.1 17.3 8.5 7.8 29.4
Health Service Use Variables
Oxygen Equipment 1.8 0.0 10.6 6.6 3.2 4.2 2.9
Visiting Nurse Services 3.5 0.1 11.2 9.5 8.9 0.6 17.5
Therapist Services 1.4 0.3 8.7 2.9 2.2 0.9 5.2
Home Health Aide Services 5.0 0.2 22.7 12.6 12.8 1.5 22.5
Social Worker Services 2.3 0.1 17.3 4.9 4.3 0.7 9.8
Adult Day Health Services 1.1 0.2 1.6 3.1 1.6 0.9 5.2
Transportation Assistance 7.1 0.5 58.1 20.2 17.4 4.9 13.1
Meals Delivered to Home 3.4 0.4 16.6 11.8 9.2 3.0 7.1
Hospital Admissions in Past Year:
None 76.8 89.1 0.0 67.9 71.8 60.7 65.2
1-3 22.0 10.8 90.0 30.0 27.1 36.9 32.3
4 or More 1.2 0.1 10.0 2.1 1.1 2.5 2.6
Nursing Home Use:
None 99.1 99.9 96.5 97.7 99.1 99.7 94.5
1-30 Days 0.4 0.1 3.3 0.8 0.4 0.2 1.4
31 Days or More 0.5 0.0 0.3 1.5 0.5 0.1 4.1
Considering Applying to Nursing Home 1.2 0.3 3.6 4.5 1.4 0.6 5.1

SOURCES: Data derived from health screening forms (HSFs) and comprehensive assessment forms (CAFs) administered by the authors. HSF data were collected from fee-for-service beneficiaries at baseline and from S/HMO enrollees upon application. Total HSF sample size is 27,503 cases. CAFs were completed semiannually by persons who identified functional disabilities on the HSF.

Approximately 93.6 percent of the “healthy” group report good or excellent health; 100 percent of the “acutely ill” group report fair or poor health. Persons in the “impaired” group (48.9 percent reporting fair or poor health) are similar to those in the “pulmonary” group (38.3 percent), while the “cardiac” (65.2 percent fair or poor) and “frail” (60.1 percent fair or poor) groups are similar. Case mix is not strongly associated with age because health changes (gikt) estimated from the combined HSF and CAF data, represent most age effects. Healthy individuals are young—a mean age of 71.7. The frail group members are the oldest, with a mean age of 83.2. Acutely ill persons are older (77.5) than the healthy, but are little different than the two chronically ill groups.

There are also large differences in service use. Acutely ill individuals use the most acute care (e.g., oxygen, 10.6 percent; visiting nurses, 11.2 percent; home health aides, 22.7 percent), and 100 percent had prior hospital stays. Prior hospital use for the impaired and pulmonary groups is similar—and three times that of the healthy group. Hospital use in the cardiac and frail groups is similar; the frail group used the most nursing homes, visiting nurses, home health, and transport services. These groups are similar to those produced from the baseline HSF data (Manton et al., 1994). In the combined HSF and CAF data, the pulmonary group is more impaired and the cardiac group has more medical problems—as does the acutely ill group. Because new health problems are recorded on CAFs, the number of disabilities and medical problems generally increased.

Health Status, Mortality, and Disenrollment

One-year probabilities of change in coverage and mortality for case-mix groups estimated from transition variables λkn(l1l2) are in Table 3. The HMO category represents the experience of FFS clients (n = 900) entering an HMO during the study.

Table 3. Annual Functional Impairment, Coverage Change, and Mortality Probabilities, by Case-Mix Group and Health Coverage: 1986-89.

Case-Mix Group and Health Coverage Health Assessment1 Change in Coverage Death

S/HMO HMO FFS

Percent
Case-Mix Standardized Rate
S/HMO 38.0 3.9 9.4 10.1
FFS 21.8 0.9 15.2 10.2
HMO2 18.4 0.4 31.9 10.6 8.1
Healthy
S/HMO 3.6 5.8 10.7 3.0
FFS 1.2 1.2 20.7 3.7
HMO2 0.5 0.2 36.8 9.8 3.0
Acutely III
S/HMO 6.6 1.8 27.2 6.4
FFS 1.0 1.6 14.4 9.5
HMO2 1.2 0.9 34.6 16.5 9.0
Impaired
S/HMO 75.4 3.4 11.5 22.1
FFS 76.1 0.7 11.2 14.4
HMO2 28.2 0.2 43.7 10.8 12.3
Pulmonary
S/HMO 80.9 1.2 4.9 7.4
FFS 56.9 0.3 6.6 12.1
HMO2 46.7 2.4 21.2 12.6 9.3
Cardiac
S/HMO 40.1 4.1 8.8 8.6
FFS 7.6 0.7 16.4 22.4
HMO2 6.9 0.3 32.8 13.1 10.9
Frail
S/HMO 78.8 0.6 3.4 51.7
FFS 70.2 0.3 3.2 28.2
HMO2 78.9 0.8 5.2 9.5 30.3
1

This column refers to the annual probability of receiving a comprehensive assessment form (CAF), issued when a change in health or a functional impairment was reported. After initial issuance, a CAF was refilled every 6 months.

2

This refers to persons in either FFS or S/HMOs who entered HMOs after the start of the study.

NOTES: S/HMO is social/health maintenance organization. HMO is health maintenance organization. FFS is fee-for-service. Probabilities are annualized and may not sum to 100 percent.

SOURCES: Data derived from health screening forms (HSFs) and CAFs administered by the authors. HSF data were collected from FFS beneficiaries at baseline and from S/HMO enrollees upon application. Total HSF sample size is 27,503 cases. CAFs were completed semiannually by persons who identified functional disabilities on the HSF.

Health Assessment

A CAF is used to assess health changes. For S/HMO members this may occur after a clinical encounter. In the FFS evaluation, data were not collected on clinical encounters. Instead, a re-HSF or re-CAF is given every 6 months to impaired persons, and everyone is screened annually. It is unlikely that changes in chronic disabilities are missed in a 6-month interval (Manton, Vertrees, and Clark, 1993).

Healthy (3.6 percent) and acutely ill (6.6 percent) S/HMO enrollees have a greater (but still relatively insignificant) chance of receiving a CAF than FFS sample members. S/HMO and FFS CAF rates are similar for impaired groups. Frail HMO members have CAF rates similar to FFS and S/HMOs. The largest S/HMO and FFS differences are for chronically ill groups. Though S/HMOs have a higher case-mix adjusted probability of a CAF than FFS (i.e., 38 percent versus 21.8 percent), the case-mix weighted time between CAFs is 38.4 days shorter in FFS.

CAF rates for S/HMOs may be higher in the healthy, acutely and chronically ill groups because of a greater likelihood of clinical encounters for acute conditions. A CAF, however, is needed to qualify for LTC. Frail cases enrolled in S/HMOs, at baseline, were more severely ill and younger than in FFS. Though not likely to stay frail (i.e., to recover or die), they had high initial costs (Manton et al., unpublished). Thus, despite the higher S/HMO CAF rates, it is unclear that clinical encounters uncover more chronic disability than the periodic and comprehensive FFS screening.

Changes in Coverage

This category includes persons who moved from: FFS to an HMO; an S/HMO (or HMO) to another HMO; an S/HMO (or HMO) to FFS. Annually, 15.2 percent of FFS clients enroll in HMOs; 10.6 percent return to FFS. Approximately 3.9 percent and 9.4 percent of S/HMO members (case-mix adjusted) enroll in HMOs and return to FFS, respectively. Healthy FFS cases are more likely to join HMOs (20.7 percent) than the acutely ill (14.4 percent). The FFS impaired (11.2 percent) and cardiac (16.4 percent) groups are also likely to enter HMOs. The FFS pulmonary group is less likely (6.6 percent), and the frail least likely (3.2 percent) to enter HMOs.

Approximately one-third (31.9 percent) of the 900 HMO enrollees switch plans annually—more than in baseline HMO samples. S/HMO members, partly because a large proportion in two sites (40 percent and 60 percent) enrolled from the parent HMO, are stable (Harrington, Newcomer, and Preston, 1993; Newcomer, Preston, and Harrington, 1991). Among recent HMO enrollees, only the pulmonary (21.2 percent) and frail (5.2 percent) groups do not switch often. Less than 6 percent of S/HMO members in any group switch to HMOs. For the acutely ill or frail, the rate is less than 2 percent. This is consistent with HMO joiners adjusting to new plans and S/HMO members having stable plan relations.

Acutely ill S/HMO enrollees are more likely than HMO members to return to FFS (27.2 percent versus 16.5 percent), as are the healthy and the impaired enrollees. Disenrollment varies by site. The two new plans disenroll more acutely ill persons than S/HMOs in mature HMOs. There is little difference between S/HMO and HMO enrollees with respect to healthy and impaired groups. S/HMO members in the chronically ill or frail groups are less likely than HMO joiners to return to FFS.

Mortality

FFS mortality (gender and age combined) is higher for the healthy, acutely and chronically ill and lower for the impaired groups. “Case-mix standardized” values are weighted to the pooled case mix of the S/HMO and FFS populations. FFS clients enrolling in HMOs had the lowest mortality (8.1 percent). S/HMO (10.1 percent) and FFS (10.2 percent) rates are similar. Case-mix measures estimated from the pooled HSF/CAF data explain most S/HMO and FFS mortality differences. The HSF data alone explain only 82 percent of mortality differences.

Stochastic Health Changes and Modality

The number of factors that can be simultaneously controlled by stratification is limited. Consequently we used a multivariate model to control for health inputs, gender, age, and coverage in examining what happens in a cohort simultaneously subjected to mortality and disability dynamics. From data available for 3 years, the difference equations were used to construct S/HMO or FFS cohort life tables. Cohort estimates reflect differences in initial case-mix distributions as well as age-dependent dynamics. To examine how disability and mortality interact in FFS and S/HMOs, we calculated three types of life tables. Table 5 presents the age-specific life expectancies and number of years expected to be lived in each case-mix group. In Tables 6 and 7, cohort health changes, mortality, and the proportion expected to be active at specific ages are calculated—starting from specific groups to adjust for initial case-mix differences. In Table 8, the effects of case-mix dynamics are removed by starting cohorts at specific ages and, holding case-mix constant, identifying S/HMO and FFS differences in mortality over age (rather than just at 75 years of age, as in Table 4).

Table 5. Life Expectancy and Active Life Expectancy by Age, Health Coverage, and Case-Mix Group, by Gender.

Gender, Age, and Health Coverage Life Expectancy Case-Mix Group1

Healthy Acutely III Impaired Pulmonary Cardiac Frail
Males
65 Years:
FFS 15.2 10.7
(70.8)
0.2
(1.6)
0.1
(0.8)
1.4
(9.4)
2.3
(15.2)
0.3
(2.2)
S/HMO 14.9 13.2
(88.8)
0.4
(2.6)
0.1
(1.0)
0.1
(1.0)
0.9
(6.0)
0.1
(0.7)
75 Years:
FFS 11.3 8.5
(75.3)
0.4
(3.2)
0.5
(4.0)
0.6
(5.0)
1.2
(11.0)
0.1
(1.0)
S/HMO 9.6 8.0
(83.2)
0.3
(2.8)
0.1
(1.5)
0.4
(4.0)
0.6
(6.0)
0.2
(2.5)
85 Years:
FFS 7.1 4.6
(65.4)
0.2
(2.9)
0.5
(7.7)
1.0
(14.3)
0.4
(6.3)
0.2
(3.5)
S/HMO 5.6 4.1
(73.4)
0.2
(4.0)
0.1
(2.3)
0.5
(9.5)
0.3
(5.5)
0.3
(5.4)
95 Years:
FFS 3.6 1.4
(40.3)
0.3
(8.6)
0.2
(5.6)
0.7
(18.2)
0.4
(10.2)
0.6
(17.1)
S/HMO 2.7 1.8
(63.9)
0.2
(7.3)
0.1
(2.1)
0.1
(4.3)
0.2
(6.6)
0.4
(15.8)
Females
65 Years:
FFS 21.4 18.7
(87.2)
0.5
(2.3)
0.4
(2.0)
0.2
(1.1)
1.4
(6.6)
0.1
(0.7)
S/HMO 18.4 16.1
(87.4)
0.5
(2.8)
0.3
(1.6)
0.1
(0.3)
1.3
(7.3)
0.1
(0.6)
75 Years:
FFS 15.1 13.0
(86.2)
0.2
(1.6)
0.3
(2.2)
0.6
(4.0)
0.6
(4.2)
0.3
(1.9)
S/HMO 11.9 9.2
(77.6)
0.3
(2.3)
0.2
(2.1)
0.9
(7.5)
1.0
(8.3)
0.3
(2.2)
85 Years:
FFS 9.2 6.3
(69.1)
0.2
(1.9)
0.6
(6.1)
1.5
(15.9)
0.3
(3.6)
0.3
(3.5)
S/HMO 6.5 3.6
(56.0)
0.2
(3.1)
0.3
(4.8)
1.3
(19.8)
0.6
(8.7)
0.5
(7.6)
95 Years:
FFS 4.6 1.7
(36.5)
0.3
(6.0)
0.2
(5.2)
0.9
(19.1)
0.4
(8.5)
1.1
(24.7)
S/HMO 3.4 1.1
(32.8)
0.3
(7.4)
0.2
(6.9)
0.9
(26.7)
0.2
(5.0)
0.7
(20.4)
1

Years of life expectancy at age X and proportion surviving.

NOTES: FFS is fee-for-service. S/HMO is social/health maintenance organization. Numbers in parentheses are in percent.

SOURCE: Data derived from health screening forms (HSFs) and comprehensive assessment forms (CAFs) adminstered by the authors. HSF data were collected from FFS beneficiaries at baseline and from S/HMO enrollees upon application. Total HSF sample size is 27,503 cases. CAFs were completed semiannually by persons who identified functional disabilities on the HSF.

Table 6. Health and Mortality Variables for Males at 75 and 85 Years of Age, by Case-Mix Group at 65 Years of Age.

Age at Evaluation Case-Mix Group at 65 Years of Age Health Coverage Life Expectancy Proportion Surviving in Percent Case-Mix Group at Evaluation Age

Healthy Acutely III Impaired Pulmonary Cardiac Frail
75 Years Healthy FFS 12.5 73.9 94.3 1.1 0.8 1.8 1.5 0.6
S/HMO 9.8 71.0 88.3 2.2 1.1 3.5 2.9 2.2
Acutely III FFS 9.9 46.2 47.3 6.7 14.9 9.9 17.7 3.5
S/HMO 8.3 41.0 56.9 14.8 3.8 9.6 9.4 5.6
Impaired FFS 10.9 57.2 66.2 4.7 11.4 6.6 8.8 2.4
S/HMO 7.8 25.9 49.9 6.3 23.0 6.8 10.0 4.0
Pulmonary FFS 9.3 38.1 37.6 7.9 11.3 14.0 24.7 4.4
S/HMO 8.5 33.3 61.7 6.2 3.6 11.0 11.9 5.6
Cardiac FFS 8.5 35.1 25.3 5.9 7.9 10.4 47.4 3.2
S/HMO 7.5 40.2 22.8 3.9 3.4 6.7 59.7 3.6
Frail FFS 9.3 31.7 37.3 8.1 11.6 14.4 24.1 4.6
S/HMO 8.4 15.5 57.9 8.5 3.3 8.8 16.4 5.1
85 Years Healthy FFS 7.4 44.2 75.2 2.2 5.0 12.4 2.5 2.8
S/HMO 5.6 32.0 74.5 3.8 2.2 9.4 4.9 5.3
Acutely III FFS 6.7 20.4 53.7 3.6 12.2 16.5 9.6 4.4
S/HMO 5.5 14.5 69.8 4.8 2.6 10.2 6.9 5.8
Impaired FFS 7.0 28.9 62.1 3.1 9.9 14.9 6.1 3.8
S/HMO 5.5 8.4 69.3 4.7 2.9 10.1 7.2 5.8
Pulmonary FFS 6.6 15.4 49.5 3.9 12.4 17.6 12.0 4.6
S/HMO 5.5 12.1 70.3 4.5 2.5 10.0 7.1 5.7
Cardiac FFS 6.4 12.4 42.0 4.3 12.2 18.0 18.8 4.7
S/HMO 5.3 11.8 58.8 5.4 3.3 10.8 15.6 6.2
Frail FFS 6.6 12.8 49.5 3.9 12.5 17.7 11.9 4.6
S/HMO 5.5 5.6 69.1 4.6 2.6 10.1 7.8 5.8

NOTES: FFS is fee-for-service. S/HMO is social/health maintenance organization.

SOURCES: Data derived from health screening forms (HSFs) and comprehensive assessment forms (CAFs) administered by the authors. HSF data were collected from FFS beneficiaries at baseline and from S/HMO enrollees upon application. Total HSF sample size is 27,503 cases. CAFs were completed semiannually by persons who identified functional limitations on the HSF.

Table 7. Health and Mortality Variables for Females at 75 and 85 Years of Age, by Case-Mix Group at 65 Years of Age.

Age at Evaluation Case-Mix Group at 65 Years of Age Health Coverage Life Expectancy Proportion Surviving in Percent Case-Mix Group at Evaluation Age

Healthy Acutely III Impaired Pulmonary Cardiac Frail
75 Years Healthy FFS 15.7 85.4 94.1 0.7 0.8 2.3 1.1 1.0
S/HMO 12.1 81.7 84.5 1.6 1.4 6.3 4.4 1.8
Acutely III FFS 12.1 52.5 38.6 8.4 10.1 16.1 18.7 8.1
S/HMO 10.1 50.1 36.3 15.8 6.1 17.8 18.2 5.9
Impaired FFS 12.5 59.8 43.7 7.5 17.0 12.5 12.2 7.2
S/HMO 10.0 49.0 31.9 7.6 20.5 15.4 19.6 5.0
Pulmonary FFS 11.5 48.7 31.1 6.7 8.6 14.6 31.8 7.2
S/HMO 10.2 45.7 36.6 6.7 6.2 18.7 25.9 6.1
Cardiac FFS 11.4 48.1 29.6 6.5 8.3 14.4 34.2 7.0
S/HMO 10.1 61.1 20.7 4.1 4.9 13.6 53.0 3.6
Frail FFS 12.5 52.8 43.8 8.7 10.4 16.2 12.7 8.3
S/HMO 10.6 26.6 47.6 6.6 5.9 15.5 18.1 6.2
85 Years Healthy FFS 9.3 62.9 73.4 1.6 4.7 14.6 2.6 3.2
S/HMO 6.5 49.2 57.6 3.0 4.5 19.4 8.0 7.5
Acutely III FFS 8.3 28.6 46.5 3.5 13.6 23.2 8.1 5.1
S/HMO 6.3 23.4 47.5 3.9 6.2 22.4 11.6 8.4
Impaired FFS 8.4 34.0 48.9 3.3 14.3 21.6 7.0 4.9
S/HMO 6.3 22.3 46.6 3.8 7.1 22.2 11.9 8.3
Pulmonary FFS 8.2 24.8 42.9 3.6 14.0 24.1 10.1 5.3
S/HMO 6.3 21.6 47.1 3.7 6.3 22.2 12.4 8.3
Cardiac FFS 8.2 24.1 42.6 3.6 14.1 24.3 10.5 5.3
S/HMO 6.2 27.9 41.8 3.9 6.9 23.1 15.9 8.4
Frail FFS 8.4 29.9 48.9 3.4 13.1 22.5 7.1 5.0
S/HMO 6.4 13.3 49.8 3.6 5.9 21.6 11.1 8.1

NOTES: FFS is fee-for-service. S/HMO is social/health maintenance organization.

SOURCES: Data derived from health screening forms (HSFs) and comprehensive assessment forms (CAFs) administered by the authors. HSF data were collected from FFS beneficiaries at baseline and from S/HMO enrollees upon application. Total HSF sample size is 27,503 cases. CAFs were completed semiannually by persons who identified functional limitations on the HSF.

Table 8. Life Expectancy, by Age, Health Coverage, and Case-Mix Group, by Gender.

Gender, Age, and Health Coverage Case-Mix Group1

Healthy Acutely III Impaired Pulmonary Cardiac Frail
Males
65 Years:
FFS 23.6 10.3 12.3 8.7 8.0 5.1
S/HMO 23.7 14.5 7.6 8.1 11.4 2.4
75 Years:
FFS 19.7 8.2 9.9 6.9 6.3 4.0
S/HMO 18.8 11.0 5.6 5.9 8.6 1.7
85 Years:
FFS 16.3 6.5 7.9 5.4 5.0 3.1
S/HMO 14.6 8.2 4.0 4.3 6.3 1.1
95 Years:
FFS 13.5 5.2 6.3 4.3 3.9 2.4
S/HMO 11.2 6.0 2.8 3.0 4.5 0.8
Females
65 Years:
FFS 33.4 17.7 14.8 13.0 10.9 7.4
S/HMO 37.1 18.2 14.3 14.6 20.6 3.7
75 Years:
FFS 27.9 13.9 11.5 10.0 8.4 5.5
S/HMO 31.7 14.7 11.4 11.6 16.8 2.8
85 Years:
FFS 23.0 10.8 8.8 7.6 6.3 4.1
S/HMO 27.0 11.7 9.0 9.2 13.5 2.1
95 Years:
FFS 19.0 8.3 6.7 5.7 4.7 3.0
S/HMO 23.2 9.3 7.0 7.2 10.8 1.6
1

Years of remaining life after age χ in each case-mix group.

NOTES: FFS is fee-for-service. S/HMO is social/health maintenance organization.

SOURCES: Data derived from health screening forms (HSFs) and comprehensive assessment forms (CAFs) administered by the authors. HSF data were collected from FFS beneficiaries at baseline and from S/HMO enrollees upon application. Total HSF sample size is 27,503 cases. CAFs were completed semiannually by persons who identified functional limitations on the HSF.

Table 4. Mortality Functions, by Case-Mix Group and Health Coverage, by Gender, at 75 Years of Age.

Case-Mix Group and Health Coverage Case-Mix Group

Healthy Acutely III Impaired Pulmonary Cardiac Frail
Males*
Healthy:
FFS 3.2
(±0.40)
15.7
(±0.60)
15.1
(±0.63)
6.3
(±0.68)
16.6
(±0.64)
18.6
(±1.04)
S/HMO 2.9
(±0.40)
4.3
(±0.85)
6.5
(±1.54)
6.3
(±1.08)
5.0
(±0.80)
12.9
(±1.57)
Acutely III:
FFS 19.9
(±1.78)
8.8
(±1.26)
111.0
(±1.38)
111.5
(±1.43)
115.0
(±1.96)
S/HMO 6.2
(±2.42)
9.6
(±2.74)
9.2
(±2.14)
7.4
(±1.66)
18.9
(±3.8)
Impaired:
FFS 17.9
(±1.78)
19.8
(±1.41)
110.3
(±1.46)
113.4
(±1.97)
S/HMO 14.7
(±6.80)
14.2
(±3.72)
11.3
(±3.04)
29.0
(±6.9)
Pulmonary:
FFS 12.2
(±2.20)
112.8
(±1.62)
116.6
(±2.20)
S/HMO 13.7
(±4.24)
10.9
(±2.30)
28.0
(±4.9)
Cardiac:
FFS 113.4
(±2.4)
117.4
(±2.30)
S/HMO 8.7
(±2.81)
22.3
(±4.2)
Frail:
FFS 122.6
(±4.60)
S/HMO 57.1
(±11.4)
Females**
Healthy:
FFS 1.7
(±0.23)
2.8
(±0.36)
3.2
(±0.34)
13.5
(±0.33)
14.0
(±0.32)
15.1
(±0.45)
S/HMO 1.6
(±0.25)
2.7
(±0.51)
3.2
(±0.85)
3.1
(±0.51)
2.5
(±0.43)
7.2
(±0.85)
Acutely III:
FFS 4.7
(±0.94)
5.4
(±0.69)
5.9
(±0.69)
16.6
(±0.75)
18.5
(±0.96)
S/HMO 4.6
(±1.60)
5.4
(±1.66)
5.4
(±1.17)
4.2
(±0.96)
12.4
(±2.32)
Impaired:
FFS 6.1
(±1.02)
6.7
(±0.70)
17.5
(±0.76)
19.7
(±0.97)
S/HMO 6.4
(±3.38)
6.4
(±1.74)
5.0
(±1.50)
14.6
(±3.86)
Pulmonary:
FFS 17.3
(±0.96)
18.2
(±0.71)
110.6
(±0.91)
S/HMO 6.3
(±1.75)
4.9
(±1.04)
14.4
(±2.24)
Cardiac:
FFS 19.2
(±1.06)
11.8
(±0.96)
S/HMO 3.9
(±1.36)
11.3
(±2.22)
Frail:
FFS 115.2
(±1.77)
S/HMO 33.2
(±5.66)
*

θFFS = 0.027, χ2 = 587.6, Ratio (6/1) = 7.1

θS/HMO = 0.038, χ2 = 643.9, RR = 19.7

**

θFFS = 0.034, χ2 = 1334.3, RR = 8.9

θS/HMO = 0.030, χ2 = 736.8, RR = 20.8

1

FFS two standard deviation bound for coefficient does not contain S/HMO estimate.

NOTES: FFS Is fee-for-service. S/HMO is social/health maintenance organization. Underlined rates indicate the higher of the two rates In the S/HMO and FFS comparison.

SOURCES: Data derived from health screening forms (HSFs) and comprehensive assessment forms (CAFs) administered by the authors. HSF data were collected from FFS beneficiaries at baseline and from S/HMO enrollees upon application. Total HSF sample size is 27,503 cases. CAFs were completed semiannually by persons who identified functional disabilities on the HSF.

Mortality Functions

Table 4 presents gender-specific estimates of FFS and S/HMO mortality (i.e., the Qt). All four have significant χ2. Each is estimated with its own θ to adjust for different unobserved age-related risk factors (i.e., bias). The coefficients represent the annual probability of death (× 100) at 75 years of age. Diagonal coefficients are the probability of death for a person in a case-mix group (e.g., the probability of death for a male whose gik = 1.0 in an S/HMO is 57.1 percent; in the healthy group, 2.9 percent). The relative risk of frail to healthy groups is 19.7 to 1 (compared with Table 3, 19.8 to 1.0; in baseline data the ratio is 10.5 to 1). If a person is represented by multiple profiles, off-diagonal (interaction) terms are used. For example, the mortality for a person whose health status is a mixture of the attributes of the frail and healthy groups is the weighted sum of the diagonal and interaction coefficients for the two groups.

Impaired and frail males have significantly higher mortality in S/HMOs (Table 3). FFS mortality is higher for the acutely ill, cardiac, and pulmonary groups, except if sharing attributes with an impaired group, due to interactions. Because impairment increases with age, this gives FFS males a mortality advantage at later ages—along with two other factors. The first is that θ, representing unobserved age-related factors, raises mortality 2.7 percent per year for FFS males, and 3.8 percent per year for S/HMO males. For each year of age, mortality rises 40.7 percent faster for S/HMO males because of non-health factors. Second, the mortality ratio of frail to healthy groups is greater in S/HMOs (19.7 to 1) than in FFS (7.1 to 1). Thus, as disability dynamics move persons into frail groups with age, mortality increases more rapidly for S/HMO males.

For females, there are no significant mortality differences for the healthy, acutely ill, or impaired groups. Two differences for the pulmonary group are marginally significant. Significant differences exist for the cardiac and frail groups. S/HMO females in the cardiac and pulmonary groups are advantaged. FFS females in the frail group, including its interactions with all other groups (except the cardiac), are advantaged. The interaction involving the frail and pulmonary groups is significant, and shows a favorable effect for FFS females. Because the cardiac group is younger (mean age 80.1 years) and the frail older (83.2 years), FFS females will be advantaged at later ages. The θ shows mortality increases 12.8 percent less per year as S/HMO females age. This is counterbalanced by disability dynamics moving more females with age into the frail group, where FFS females have better survival. The effects of greater heterogeneity (i.e., a frail-to-healthy relative risk of 20.8 to 1 versus 8.9 to 1 in FFS) also favors FFS female survival.

Active Life Expectancy Estimates

We used equations 7 through 12 to estimate cohort life tables using parameters from equations 6 and 7. At the left of Table 5 we list age and coverage. Next are age-specific life expectancies and then six columns containing the years expected to be lived at age χ in a case-mix group (ekχ)—underneath each ekχ is the proportion that those years represent of life expectancy at that age. Male life expectancy at 65 years of age is 15.2 years in FFS and 14.9 years in S/HMO. The proportion of ALE (13.2 years; 88.8 percent) in S/HMOs is higher than in FFS (10.7 years; 70.8 percent), despite a lower life expectancy. Male life expectancy is higher in FFS to 95 years of age with absolute ALE differences becoming small by 75 years of age (i.e., 8.5 years in FFS; 8.0 years in S/HMO).

For females, life expectancy at 65 years of age is 3 years higher in FFS (21.4 years) than in S/HMOs (18.4 years). The ALE proportion is similar (87.2 percent versus 87.4 percent) at 65 years of age, though the absolute difference is 2.6 years because of higher FFS life expectancy. At 75 years of age, ALE is absolutely and proportionately higher in FFS (e.g., 86.2 percent versus 77.6 percent).

For both genders the proportion of life lived frail is modestly higher in FFS at 65 years of age and 95 years of age. It is higher in S/HMOs at 75 years of age and 85 years of age. Because the frail have a high risk of institutionalization, it may be that the frail's greater prevalence in FFS at 95 years of age reflects nursing home restrictions in certifiable S/HMOs.

Age-Specific Proportions in Case-Mix States

The life tables in Table 5 reflect the case-mix distribution at enrollment (i.e., initial conditions for the different equations), which is favorably biased for S/HMOs. To control for this, Tables 6 and 7 present case-mix distributions for 10-and 20-year survivors of cohorts starting in the Kth case-mix group at 65 years of age—specific to gender and coverage. These provide, for each group, estimates of the expected number of remaining years of life at a given age (e.g., 75 years of age and 85 years of age), the proportion surviving a period, and the likelihood of changing case mix.

Healthy males 65 years of age have a life expectancy at 75 years of age of 12.5 years (FFS) and 9.8 years (S/HMO), with 73.9 percent (FFS) and 71.0 percent (S/HMO) surviving 10 years. Males who are frail at 65 years of age have a life expectancy at 75 years of age of 9.3 years (FFS) and 8.4 years (S/HMO), with 37.3 percent and 57.9 percent becoming healthy after 10 years. By 85 years of age, 44.2 percent of healthy FFS males are alive; 32 percent in S/HMOs. Similar proportions of surviving males stay healthy (75.2 percent versus 74.5 percent). Of the frail, only 12.8 percent (FFS) and 5.6 percent (S/HMO) survive 20 years. Of frail survivors, 49.5 percent in FFS and 69.1 percent in S/HMOs become healthy by 85 years of age. The higher proportions becoming healthy in S/HMOs may be because of attrition (i.e., a smaller proportion of the frail survive in S/HMOs).

In Table 7, life expectancy is higher for FFS females at 75 years of age and 85 years of age. FFS has more healthy females (62.9 percent) surviving to 85 years of age than S/HMOs (49.2 percent). Survival is greater in FFS in all groups except the cardiac. S/HMO females in the cardiac group had better survival at both 75 years of age and 85 years of age. The frail group shows the greatest differences-more than one-half (52.8 percent) of frail FFS females survive 10 years (i.e., to 75 years of age), compared with 26.6 percent of frail S/HMO females. S/HMOs, by restricting nursing home certifiable cases, may attract acutely ill and frail persons. By 75 years of age, one-half the frail female survivors in both types of coverage return to the healthy group.

In Table 8 we set auto-regressive coefficients to 1.0 (βkk = 1) and diffusion Σ = 0 to remove the effects of health changes. Comparing Table 8 with Tables 6 and 7 identifies the effects of health changes. Table 8, for example, shows that frail males have a life expectancy at 65 years of age of 5.1 years in FFS and 2.4 years in S/HMOs. Life expectancy at 65 years of age in Tables 6 and 7 is higher because persons can either die or change health status. In Table 8, FFS healthy, impaired, and frail males live longer past 75 years of age. S/HMO males live longer only in the acutely ill and cardiac groups. S/HMO females are advantaged in the cardiac, healthy, acutely ill, and impaired groups. A survival advantage exists for FFS females manifesting attributes of the frail. Because the prevalence of frailty increases with age, this mortality advantage increased in Table 7, where disability dynamics were operating.

A comparison of Tables 5 through 8 isolates gender differences between outcomes in the two types of coverage attributable to initial conditions, health change, and mortality. For example, while FFS males have modestly better survival but worse ALE than S/HMO males in Table 5 because of better initial conditions in S/HMOs, this changes in Table 6, with initial condition differences eliminated, where the proportion active stays higher for FFS males. For FFS females, life expectancy at 65 years of age is greater (3 years) because groups where mortality differences favor FFS females are those into which disability dynamics, identified in Table 7, move females with age. Table 8 describes the pure effects of mortality free of disability dynamics—one component of the cohort experience.

Gender differences between FFS and S/HMO, because θs are non-zero and differ in size, may reflect differences in unobserved factors (e.g., widowhood). Without estimating θ, this effect would be subsumed in Q, causing those coefficients to be biased. The Qt include these effects but are evaluated at specific ages. Females have higher institutional risks above 85 years of age. For the elderly, the prevalence of dementia above 85 years of age could be as high as 47 percent (Evans et al., 1992) with 10 percent severely demented. Though having high disability, Alzheimer's cases can have near normal life spans with good care. The initial exclusion of institutionalized persons at all ages, given a high prevalence of dementia in institutions, removes many elderly, demented persons from S/HMO eligibility. However, one could expect moderately demented elderly to be disproportionately FFS clients (i.e., impaired groups tend to re-enter FFS).

Outcome Differences by Site and Gender

To ascertain whether outcome differences are related to site, or to whether a S/HMO was established in a pre-existing HMO or a LTC organization, we calculated life tables for total and site-specific populations. The results are presented in Table 9.

Table 9. Comparison of Life Expectancy and Active Life Expectancy, by Site and Type of Health Coverage, by Age and Gender.

Health Coverage and Site Life Expectancy at Age Proportion Active at Age


65 Male Female 85 Male Female 75 Male Female 85 Male Female

Percent
S/HMO 16.85 14.9 18.4 6.09 5.6 6.5 79.7 62.3
FFS 17.83 15.2 21.4 6.98 7.1 9.2 81.7 69.0
Δ 1.01 0.89 2.0 6.7
Established in HMOs
Minneapolis:
S/HMO 17.83 15.8 19.2 6.37 5.7 7.0 80.1 82.6 79.3 63.0 68.1 60.9
FFS 18.35 16.3 21.7 7.36 7.7 10.1 82.1 84.3 81.4 69.6 73.7 67.7
Δ 0.52 0.5 2.5 1.02 2.0 3.1 2.0 1.7 2.1 6.6 5.6 6.8
Portland:
S/HMO 16.71 14.2 18.4 5.86 5.6 6.5 79.2 80.5 78.6 61.4 64.8 59.7
FFS 16.96 14.4 18.7 6.67 6.3 8.2 81.5 82.8 80.8 68.5 71.6 66.8
Δ 0.25 0.2 0.3 0.81 0.7 1.7 2.3 2.3 2.2 7.1 7.2 7.1
Established in LTC Organizations
Brooklyn:
S/HMO 16.61 14.0 19.2 6.37 5.0 7.7 80.4 82.4 79.2 63.2 68.4 60.0
FFS 17.14 14.4 19.9 7.39 5.9 8.9 82.3 84.3 81.1 69.6 74.1 66.6
Δ 0.53 0.4 0.7 1.02 0.9 1.2 1.9 1.9 1.9 6.4 5.7 6.6
Long Beach:
S/HMO 16.49 13.8 18.1 6.24 5.2 6.7 80.9 83.7 79.6 64.1 70.5 61.3
FFS 16.96 14.4 18.5 7.22 6.3 7.7 82.9 85.1 81.7 70.6 75.2 68.4
Δ 0.47 0.6 0.4 0.98 1.1 1.0 2.0 1.4 2.1 5.9 4.9 7.1

NOTES: S/HMO is social/health maintenance organization. FFS is fee-for-service. LTC is long-term care. Delta represents difference between S/HMO and FFS.

SOURCES: Data derived from health screening forms (HSFs) and comprehensive assessment forms (CAFs) administered by the authors. HSF data were collected from FFS beneficiaries at baseline and from S/HMO enrollees upon application. Total HSF sample size is 27,503 cases. CAFs were completed semiannually by persons who identified functional limitations on the HSF.

There are differences in life expectancy at 65 years of age (1.01 years) and 85 years of age (0.89 year) that favor FFS. Likewise, the proportion of individuals active at 75 years of age is higher in FFS (2.0 percent), with the difference increasing with age (at 85 years of age it is 6.7 percent).

Site-specific results show that FFS life expectancy is higher in all sites at 65 years of age and 85 years of age. The difference at 85 years of age is slightly larger than at 65 years of age, suggesting that it increases with time. The proportion of active individuals is higher in FFS at 75 years of age (reflecting a population that was enrolled in FFS for 10 years; a comparison at 65 years of age reflects only initial conditions) and increases at 85 years of age. The differences are similar across sites and do not vary by whether the S/HMO was started by an HMO or a LTC provider. There is a slight advantage at 85 years of age in the proportion of enrollees active in the two LTC organization-based S/HMOs (6.4 percent and 5.9 percent) over the differences relative to FFS in the two HMO-based S/HMOs (6.6 percent and 7.1 percent).

Discussion and Conclusion

S/HMOs integrate medical, health, and social services which, with financial risk, are designed to improve services and control costs. The issue addressed here is whether S/HMOs improved for members, over that for comparable FFS clients, age and gender-specific functional status, and mortality. To describe functional status, 30 items from the HSF and CAF were used to define 6 case-mix groups ranging from healthy to frail using a multivariate procedure. Groups were updated when a health change was measured in a CAF.

The case-mix groups are used to control health variation in two analyses. The first describes time to events within the 3-year study period. The second uses parameters estimated from the study to calculate cohort life tables, specific to gender and coverage. In cohort life tables, disability dynamics and mortality interact, though, by adjusting the coefficients in the difference equations, specific features of the health and mortality processes can be isolated. In the analysis of the 36 months of followup, lifetime implications of the differences between S/HMO and FFS experiences cannot be estimated. Differences in health changes past 36 months are not observed, so even censoring and “length biased” sampling will affect standard statistical analyses. The difference equations for the life table calculations allow the partial (i.e., 36 month) experience of persons at different ages to be composed to extrapolate the lifetime experience of specific cohorts using a multidimensional stochastic process model. Such calculations, though requiring assumptions about the form of the difference equations, allow estimates to be made for lifetime behavior—estimates impossible to make directly without bias with only 36 months of observation. Also, the difference equations reflect the dynamic interaction of health changes and mortality—this cannot be estimated as coefficients in a regression function. Thus, it is necessary to manipulate the difference equations, as done in Tables 5 through 8, to isolate the effects of initial conditions, health dynamics, and mortality selection for subgroups in the study. The problems of limited followup and the interaction of health changes and mortality, are found in many longitudinal observational and demonstration studies.

In Table 5, total life expectancy differed little for males, even though S/HMO males had an early ALE advantage reflecting an initially favorable case mix. For FFS females, in contrast, there is a life expectancy of 3 more years at 65 years of age; 2.6 years more of ALE. FFS life expectancy is high, relative to U.S. cross-sectional life tables (National Center for Health Statistics, 1989). However, institutionalized persons at all ages are initially “out of scope” for the FFS sample and S/HMOs. Thus, the life expectancy estimate should reflect the survival of persons of all ages initially non-institutionalized. This would have greater effects on females, persons of advanced age, and persons with dementia—all groups with high institutionalization rates. An effect of the anticipated direction and size is found in FFS but not in S/HMOs (Branch et al., 1991; Lew and Garfinkel, 1984, 1987).

Initial differences in case mix are adjusted in Tables 6 through 8 by analyzing survival and disability changes within case-mix groups. Non-response affects the proportion of cases initially in a group, but not its dynamics. Adjusting for the initial case mix (as in Tables 6 and 7) improves the relative performance of FFS clients in terms of the proportion active at specific ages. Healthy FFS clients are more likely to stay so at 75 years of age and 85 years of age. S/HMO males and females are likely to become relatively more healthy—but because of higher attrition rates in impaired groups. FFS survival is better for the impaired. Thus, while more surviving S/HMO male members are healthy, survival is worse for impaired groups, or for those with both acute illness and impairment (i.e., persons jointly in acutely ill, impaired, or frail groups). For females a mortality advantage occurs for the impaired and frail groups.

In considering outcome differences, several factors are relevant. First, it is difficult to demonstrate effects in community trials because innovation may affect controls (Brown and Mossell, 1984). If innovation is rapid, FFS clients may have access to new forms of care, while S/HMO members are restricted to a fixed set of services. The National Long-Term Care Channeling demonstration showed that controls often obtained LTC on their own (Manton, Vertrees, and Clark, 1993). Thus, what is usual and customary FFS care may change over the study, e.g., growth in the use of post-acute and home health services in the 1980s by Medicare-eligible persons (Manton et al., 1993). The out-of-pocket purchase of equipment and supplemental LTC services is further facilitated as the average income and education of new elderly cohorts increase. Therefore, S/HMO services (and their definition of and approach to “high risk” chronic care cases) have to be as adaptive as the private LTC market available for controls—especially for females—a general problem in the U.S. health care system (Ayanian and Epstein, 1991; Khan et al., 1990; Maynard et al., 1992; Steingart et al.,1991).

Second, S/HMOs are intended to allocate resources efficiently. Plans operate within benefit guidelines and LTC screening criteria, but vary in emphasis on rehabilitation or prevention. S/HMO interventions were not fixed over time, in contrast to standard clinical trials (e.g., geriatric evaluation units, where procedures for improving function and survival in the frail elderly were tested in randomized designs with fixed case and control groups [Rubenstein and Josephson, 1989]). A number of interventions have been shown in such trials to improve the health and functioning of the elderly, e.g., physical activity (Fiatarone et al., 1990), nutritional supplementation (Bastow, 1983a, 1983b; Gerster, 1991; Larsson et al., 1990; Penn et al., 1991a, 1991b; Tilyard et al., 1992), improved medical and surgical treatments (Gold et al., 1991; Hosking et al., 1989; SHEP Cooperative Research Group, 1991). S/HMO health outcomes might have improved had they adopted recently proven geriatric evaluation and treatment innovations.

This analysis, in addition to illustrating a general methodology for analyzing longitudinal studies of capitated plans, where randomization into case and control groups is inconsistent with study goals, identifies several features of S/HMO performance relative to FFS care with health policy implications.

First, it is clear, because of the large initial case-mix differences between the FFS population and those electing to enter S/HMOs, that capitation-based systems providing extended and LTC services can be more effective if rates are adjusted for detailed case-mix measures—and not just for the four average annual per capita cost factors (i.e., age, gender, Medicaid, and institutional status) that are known not to predict individual service costs. If this were done, then the problems of persons with high institutional risks and LTC needs (e.g., those with dementia, the oldest-old, females with specific health problems) could be directly addressed in capitated organization.

Second, little difference in outcome is found between S/HMOs started in established HMOs versus those started by LTC providers. In both cases acute care seems to be adequate. Neither appears to perform especially well in providing LTC—though S/HMOs started by LTC providers may do marginally better. This may be because of the restrictions placed on LTC eligibility and benefits which limit the provision of necessary LTC services.

Third, S/HMOs seem to perform HMO functions well, as indicated by the relative health success of the healthy and acutely ill. This is confirmed by the similarity of outcomes for specific case-mix groups between S/HMO enrollees and those FFS members entering HMOs during the study. However, S/HMOs perform less well for impaired persons, or for acutely ill persons with chronic impairments. Thus, LTC services provided by the S/HMOs, and their integration with acute care, do not seem effective.

This is illustrated by major gender difference in outcomes. Males, who have a lower disability prevalence, and are impaired for shorter periods of time, have similar life expectancy outcomes as seen in Table 5. FFS females have large advantages. Because females have higher disability prevalence, are disabled for longer periods of time, and, because of widowhood, are at greater risk of institutionalization, this suggests that LTC services provided in S/HMOs were not effective in improving their functional status—especially among elderly females who have the greatest LTC needs.

Gender differences are explored in a series of analyses in Tables 5 through 8. In Table 5, large differences in total life expectancy and ALE for FFS females were found even with favorable S/HMO enrollment. In Table 7, we removed the effects of favorable enrollment and still found advantages for FFS females. In Table 6, with the favorable enrollment for S/HMO males eliminated, FFS males had better outcomes. In Table 8 all disability dynamics (i.e., case-mix changes) are eliminated to generate life expectancy estimates for persons who remain in specific case-mix groups from 65 years of age. In this case, FFS males do well in all but the acutely ill and cardiac group, while only the frail do better for FFS females. Thus, the advantages observed in Tables 5 and 7 for FFS females are because of disability transitions over time and age. When disability dynamics are eliminated, the mortality patterns for each case-mix group are less favorable for FFS females (except for the frail). Thus, much of the disadvantage for S/HMO females may be because of a failure to keep persons from moving into impaired categories where FFS females are advantaged. For males, in contrast, because the age dependence of mortality (i.e., θ is smaller) is favorable for FFS, there are still improvements with age in Table 8.

Thus, the different tables isolate the effects of initial conditions (i.e., case mix at enrollment), disability changes, and mortality. FFS females have advantages in terms of disability changes. FFS males have mortality advantages at latter ages. S/HMOs start with an advantaged initial case mix. Thus, there is a need to reevaluate the LTC provided by S/HMOs to determine how to better serve the chronically disabled elderly female population and to slow their rate of disability onset. This is now more feasible than when the S/HMO demonstrations started, because a number of innovative therapies and procedures have recently been demonstrated to be effective in improving function and survival (physical therapy [Rubenstein and Josephson, 1989]; nutritional supplementation [Fiatarone et al., 1990]). Furthermore, results from national surveys (Manton, Corder, and Stallard, 1993) show that rates of disability onset have declined nationally from 1984 to 1990. Even without intervention, the general U.S. elderly population shows declines in disability. Presumably S/HMO enrollees should do better than the general population without specialized integrated care. The method of reimbursing capitated systems to provide necessary LTC services to impaired elderly must be redesigned before capitated plans can deal effectively with this portion of the health service needs of the U.S. elderly population.

Acknowledgments

We acknowledge the review and comments of our project officer, Nancy Miller, the comments offered by a Technical Advisory Panel, and the programming assistance of Frances Pendergrass and Barbara Priboth.

Support for this research was provided by the Health Care Financing Administration (HCFA) to the University of California-San Francisco (subcontract to Duke University, Center for Demographic Studies) through Contract Number 85-034/CP. Kenneth G. Manton and Gene R. Lowrimore are with Duke University, Center for Demographic Studies. Robert Newcomer and Charlene Harrington are with the University of California-San Francisco. James C. Vertrees is with SOLON Consulting, Ltd. The opinions expressed are those of the authors and do not necessarily reflect the views or policy positions of HCFA, Duke University, the University of California, or SOLON Consulting, Ltd.

Footnotes

Reprint requests: Kenneth G. Manton, Ph.D., Duke University, Center for Demographic Studies, 2117 Campus Drive, Box 90408, Durham, North Carolina 277080408.

References

  1. Ayanian JZ, Epstein AM. Differences in the Use of Procedures Between Women and Men Hospitalized for Coronary Heart Disease. New England Journal of Medicine. 1991;325:221–225. doi: 10.1056/NEJM199107253250401. [DOI] [PubMed] [Google Scholar]
  2. Bastow MD, Rawlings J, Allison SP. Undernutrition, Hypothermia, and Injury in Elderly Women with Fractured Femur: An Injury Response to Altered Metabolism? Lancet. 1983a;1:143–146. doi: 10.1016/s0140-6736(83)92754-x. [DOI] [PubMed] [Google Scholar]
  3. Bastow MD, Rawlings J, Allison SP. Benefits of Supplementary Tube Feeding After Fractured Neck or Femur: A Randomized Controlled Trial. British Journal of Medicine. 1983b;287:1589–1592. [PMC free article] [PubMed] [Google Scholar]
  4. Bishop YM, Fienberg SE, Holland PW. Discrete Multivariate Analysis: Theory and Practice. Cambridge, MA.: MIT Press; 1975. [Google Scholar]
  5. Branch LG, Guralnik JM, Foley DF, et al. Active Life Expectancy for 10,000 Caucasian Men and Women in Three Communities. Journal of Gerontology: Medical Sciences. 1991;46:M145–M150. doi: 10.1093/geronj/46.4.m145. [DOI] [PubMed] [Google Scholar]
  6. Brandeis GH, Morris JN, Nash DJ, Lipsitz LA. The Epidemiology and Natural History of Pressure Ulcers in Elderly Nursing Home Residents. Journal of the American Medical Association. 1990;264:2905–2909. [PubMed] [Google Scholar]
  7. Braun BI. The Effect of Nursing Home Quality on Patient Outcome. Journal of the American Geriatrics Society. 1991;39:329–338. doi: 10.1111/j.1532-5415.1991.tb02896.x. [DOI] [PubMed] [Google Scholar]
  8. Brown RS. Biased Selection in the Medicare Competition Demonstrations. Princeton, N.J.: Mathematica Policy Research Inc.; Mar. 1988. Prepared for Health Care Financing Administration under contract awarded in response to RFP No. HCFA-83-ORD-29/CP. [Google Scholar]
  9. Brown RS, Mossel PA. Channeling Evaluation Supplementary Report Number 3. Princeton, NJ.: Mathematica Policy Research Inc.; Oct, 1984. Examination of the Equivalence of Treatment and Control Groups and the Comparability of Baseline Data. [Google Scholar]
  10. Cox D, Hinkley D. Theoretical Statistics. London: Chapman and Hall; 1974. [Google Scholar]
  11. Cupples L, D'Agostino R, Anderson K, Kannel W. Comparison of Baseline and Repeated Measure Covariate Techniques in the Framingham Heart Study. Statistics in Medicine. 1988;7:205–218. doi: 10.1002/sim.4780070122. [DOI] [PubMed] [Google Scholar]
  12. Dontas AS, Tzonou A, Kasviki-Charvati P, et al. Survival in a Residential Home: An Eleven-Year Longitudinal Study. Journal of the American Geriatrics Society. 1991;39:641–649. doi: 10.1111/j.1532-5415.1991.tb03616.x. [DOI] [PubMed] [Google Scholar]
  13. Durako S. Evaluation of Social/Health Maintenance Organization Demonstration: Final Report on Survey Field Methods. Rockville, MD.: Westat®, Inc.; 1987. [Google Scholar]
  14. Evans DA, Scherr PA, Cook NR, et al. The Impact of Alzheimer's Disease in the United States Population. In: Suzman RW, Willis D, Manton KG, editors. The Oldest Old. New York: Oxford University Press; 1992. [Google Scholar]
  15. Fiatarone MA, Marks EC, Ryan ND, et al. High-Intensity Strength Training in Nonagenarians. Journal of the American Medical Association. 1990;263:3029–3034. [PubMed] [Google Scholar]
  16. Gerster H. Review: Antioxidant Protection of the Ageing Macula. Age and Ageing. 1991;20:60–69. doi: 10.1093/ageing/20.1.60. [DOI] [PubMed] [Google Scholar]
  17. Gloth FM, Tobin JD, Sherman SS, Hollis BW. Is the Recommended Daily Allowance for Vitamin D Too Low for the Homebound Elderly? Journal of the American Geriatrics Society. 1991;39:137–141. doi: 10.1111/j.1532-5415.1991.tb01615.x. [DOI] [PubMed] [Google Scholar]
  18. Gold S, Wong WF, Schatz IJ, Blanchette PL. Invasive Treatment for Coronary Artery Disease in the Elderly. Archives of Internal Medicine. 1991;151:1085–1088. [PubMed] [Google Scholar]
  19. Gross JS, Neufeld RR, Libow LS, et al. Autopsy Study of the Elderly Institutionalized Patient. Archives of Internal Medicine. 1988;148:173–176. [PubMed] [Google Scholar]
  20. Harrington C, Newcomer R, Preston S. A Comparison of S/HMO Disenrollees and Continuing Members. Inquiry. 1993;30:429–440. [PubMed] [Google Scholar]
  21. Hing E, Sekscenski E, Strahan G. Vital and Health Statistics. No. 97. Washington: U.S. Government Printing Office; 1989. The National Nursing Home Survey: 1985 Summary for the United States. (13). DHHS Pub. No. (PHS) 89-1758. National Center for Health Statistics. Public Health Service. [PubMed] [Google Scholar]
  22. Hosking MP, Warner MA, Ledbell CM, et al. Outcomes of Surgery in Patients 90 Years of Age and Older. Journal of the American Medical Association. 1989;261:1909–1915. [PubMed] [Google Scholar]
  23. Katz S, Akpom CA. A Measure of Primary Sociobiological Functions. International Journal of Health Services. 1976;6:493–508. doi: 10.2190/UURL-2RYU-WRYD-EY3K. [DOI] [PubMed] [Google Scholar]
  24. Katz S, Branch LG, Branson MH, et al. Active Life Expectancy. New England Journal of Medicine. 1983;309:1218–1223. doi: 10.1056/NEJM198311173092005. [DOI] [PubMed] [Google Scholar]
  25. Kemper P. The Evaluation of the National Long Term Care Demonstrations. Health Services Research. 1988;23:161–174. [PMC free article] [PubMed] [Google Scholar]
  26. Khan SS, Nessim S, Gray R, et al. Increased Mortality of Women in Coronary Artery Bypass Surgery: Evidence for Referral Bias. Annals of Internal Medicine. 1990;112:561–567. doi: 10.7326/0003-4819-112-8-561. [DOI] [PubMed] [Google Scholar]
  27. Langwell KM, Hadley JP. Evaluation of the Medicare Competition Demonstrations. Health Care Financing Review. 1989 Winter;11(2):65–80. [PMC free article] [PubMed] [Google Scholar]
  28. Larsson F, Unosson M, Ek AC, et al. Effect of Dietary Supplement on Nutritional Status and Clinical Outcome in 501 Geriatric Patients—A Randomized Study. Clinical Nutrition. 1990;9:179–184. doi: 10.1016/0261-5614(90)90017-m. [DOI] [PubMed] [Google Scholar]
  29. Lawton MP, Brody EM. Assessment of Older People: Self-Maintaining and Instrumental Activities of Daily Living. Gerontologist. 1969;9:179–186. [PubMed] [Google Scholar]
  30. Lazarsfeld PF, Henry NW. Latent Structure Analysis. Boston: Houghton Mifflin; 1968. [Google Scholar]
  31. Leutz WN, Greenberg JN, Abrahams R, et al. Changing Health Care for an Aging Society: Planning for the Social Health Maintenance Organization. Lexington, MA.: Lexington/Heath; 1985. [Google Scholar]
  32. Lew EA, Garfinkel L. Differences in Mortality and Longevity by Sex, Smoking Habits and Health Status. Transactions of the Society of Actuaries. 1987;39:107–125. [Google Scholar]
  33. Lew EA, Garfinkel L. Mortality at Ages 65 or Over in a Middle-Class Population. Transactions of the Society of Actuaries. 1984;36:257–295. [Google Scholar]
  34. Manton KG, Corder LS, Stallard E. Estimates of Change in Chronic Disability and Institutional Incidence and Prevalence Rates in the U.S. Elderly Population from the 1982,1984, and 1989 National Long-Term Care Survey. Journal of Gerontology: Social Sciences. 1993;47(4):S153–S166. doi: 10.1093/geronj/48.4.s153. [DOI] [PubMed] [Google Scholar]
  35. Manton KG, Newcomer R, Lowrimore GR, et al. A Method for Adjusting Capitation Payments to Managed Care Using Multivariate Patterns of Health and Functioning: The Experience of Social/Health Maintenance Organizations. Medical Care. 1994;32(2):277–297. doi: 10.1097/00005650-199403000-00007. [DOI] [PubMed] [Google Scholar]
  36. Manton KG, Newcomer R, Lowrimore GR, et al. Disenrollment and Mortality in Social/Health Maintenance Organizations. Unpublished. [Google Scholar]
  37. Manton KG, Stallard E, Woodbury MA. A Multivariate Event History Model Based Upon Fuzzy States: Estimation from Longitudinal Surveys with Informative Nonresponse. Journal of Official Statistics. 1991;7:261–293. Published by Statistics Sweden, Stockholm. [Google Scholar]
  38. Manton KG, Stallard E, Woodbury MA, Dowd JE. Journal of Gerontology: Biological Sciences. Time Varying Covariates in Model of Human Mortality and Aging: A Multidimensional Generalization of Gompertz. To be published. [DOI] [PubMed] [Google Scholar]
  39. Manton KG, Stallard E, Woodbury MA, Yashin AI. Applications of the Grade of Membership Technique to Event History Analysis: Extensions to Multivariate Unobserved Heterogeneity. Mathematical Modelling. 1986;7:1375–1391. [Google Scholar]
  40. Manton KG, Stallard E, Woodbury MA, Yashin AI. In: Grade of Membership Techniques for Studying Complex Event History Processes with Unobserved Covariates. Sociological Methodology, 1987. Clogg C, editor. San Francisco: Jossey-Bass; 1987. [Google Scholar]
  41. Manton KG, Vertrees JC, Clark RF. A Multivariate Analysis of Disability and Health Groups, and Their Longitudinal Change in the National Channeling Demonstration Data. The Gerontologist. 1993;33(5):610–618. doi: 10.1093/geront/33.5.610. [DOI] [PubMed] [Google Scholar]
  42. Manton KG, Woodbury MA, Tolley HD. Statistical Procedures for the Application of Fuzzy Set Models to High Dimensional Discrete Response Data. New York: John Wiley; Apr, 1994. [Google Scholar]
  43. Manton KG, Woodbury MA, Vertrees JC, Stallard E. Use of Medicare Services Before and After Introduction of the Prospective Payment System. Health Services Research. 1993;28(3):269–292. [PMC free article] [PubMed] [Google Scholar]
  44. Maynard C, Litwin PE, Martin JS, Weaver D. Gender Differences in the Treatment and Outcome of Acute Myocardial Infarction. Archives of Internal Medicine. 1992;152:972–976. [PubMed] [Google Scholar]
  45. McFarland BH, Freeborn DK, Mullooly JP, Pope CE. Utilization Patterns and Mortality of HMO Enrollees. Medical Care. 1986;24(3):200–208. doi: 10.1097/00005650-198603000-00002. [DOI] [PubMed] [Google Scholar]
  46. National Center for Health Statistics. Vital and Health Statistics. Washington: U.S. Government Printing Office; 1966. Vital and Health Statistics Data Evaluation and Methods Research, Computer Simulation of Hospital Discharges. Public Health Service (1000 Series 2 No. 13) [PubMed] [Google Scholar]
  47. National Center for Health Statistics. Health, United States, 1988. Washington: U.S. Government Printing Office; Mar, 1989. DHHS Pub. No. (PHS) 89-1232. Public Health Service. [Google Scholar]
  48. Newcomer R, Harrington C, Friedlob A. Social Health Maintenance Organizations: Assessing their Initial Experience. Health Services Research. 1990;25:242. [PMC free article] [PubMed] [Google Scholar]
  49. Newcomer R, Preston S, Harrington C. Health Plan Satisfaction Among Members of the Social/Health Maintenance Organization Machine Copy. San Francisco: University of California; 1991. [Google Scholar]
  50. Penn ND, Purkins L, Kelleher J, et al. Ageing and Duodenal Mucosai Immunity. Age and Ageing. 1991a;20:33–36. doi: 10.1093/ageing/20.1.33. [DOI] [PubMed] [Google Scholar]
  51. Penn ND, Purkins L, Kelleher J, et al. The Effect of Dietary Supplementation with Vitamins A, C and E on Cell-Mediated Immune Function in Elderly Long-Stay Patients: A Randomized Controlled Trial. Age and Ageing. 1991b;20:169–174. doi: 10.1093/ageing/20.3.169. [DOI] [PubMed] [Google Scholar]
  52. Pinchcofsky-Devin GD, Kaminski MV. Incidence of Protein Calorie Malnutrition in the Nursing Home Population. Journal of the American College of Nutrition. 1987;6(2):109–112. doi: 10.1080/07315724.1987.10720167. [DOI] [PubMed] [Google Scholar]
  53. Reuben DB, Siu AL, Kimpau S. The Predictive Validity of Self-Report and Performance-Based Measures of Function and Health. Journal of Geronotology: Medical Sciences. 1992;47(4):M106–M110. doi: 10.1093/geronj/47.4.m106. [DOI] [PubMed] [Google Scholar]
  54. Riley G, Rabey E, Kasper J. Biased Selection and Regression Toward the Mean in Three Medicare HMO Enrollees. Medical Care. 1989;27(4):337–351. doi: 10.1097/00005650-198904000-00002. [DOI] [PubMed] [Google Scholar]
  55. Rubenstein LZ, Josephson KE. Hospital Based Geriatric Assessment in the United States: The Sepulveda VA Geriatric Evaluation Unit. Danish Medical Bulletin: Gerontology Special Supplement Series. 1989;7:74–79. [Google Scholar]
  56. SHEP Cooperative Research Group. Prevention of Stroke by Antihypertensive Drug Treatment in Older Persons with Isolated Systolic Hypertension. Journal of the American Medical Association. 1991;265:3255–3264. [PubMed] [Google Scholar]
  57. Steingart RM, Packer M, Hamm P, et al. Sex Differences in the Management of Coronary Heart Disease. New England Journal of Medicine. 1991;325:226–230. doi: 10.1056/NEJM199107253250402. [DOI] [PubMed] [Google Scholar]
  58. Suzman RW, Harris T, Hadley E, Weindruch R. The Robust Oldest-Old: Optimistic Perspective for Increasing Healthy Life Expectancy. In: Suzman RW, Willis D, Manton KG, editors. The Oldest Old. New York: Oxford University Press; 1992. [Google Scholar]
  59. Tilyard MW, Spears GFS, Thomson J, Dovey S. Treatment of Postmenopausal Osteoporosis with Calcitriol or Calcium. New England Journal of Medicine. 1992;326(6):357–362. doi: 10.1056/NEJM199202063260601. [DOI] [PubMed] [Google Scholar]
  60. U.S. General Accounting Office. Medicare: Need to Strengthen Home Health Care Payment Controls and Address Unmet Needs. Washington: U.S. Government Printing Office; 1986. Pub. No. GAO/HRD-87-9. [Google Scholar]
  61. Weissert WG, Cready CM, Pawelak JE. The Past and Future of Home- and Community-Based Long-Term Care. Milbank Quarterly. 1988;66:309–388. [PubMed] [Google Scholar]
  62. Woodbury M, Clive J. Clinical Pure Types as a Fuzzy Partition. Journal of Cybernetics. 1974;4(3):111–121. [Google Scholar]
  63. Woodbury MA, Manton KG, Tolley HD. Journal of Information Sciences. A General Model for Statistical Analysis Using Fuzzy Sets: Sufficient Conditions for Identifiability and Statistical Properties. To be published. [Google Scholar]
  64. Zawadski RT, editor. Community Based System of Long-Term Care. New York: Hawthorn; 1984. [Google Scholar]

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