Context.— Health values (utilities or preferences for health states) are often
incorporated into clinical decisions and health care policy when issues of
quality vs length of life arise, but little is known about health values of
the very old.
Objective.— To assess health values of older hospitalized patients, compare their
values with those of their surrogate decision makers, investigate possible
determinants of health values, and determine whether health values change
over time.
Design.— A prospective, longitudinal, multicenter cohort study.
Setting.— Four academic medical centers.
Participants.— Four hundred fourteen hospitalized patients aged 80 years or older and
their surrogate decision makers who were interviewed and understood the task.
Main Outcome Measures.— Time–trade-off utilities, reflecting preferences for current health
relative to a shorter but healthy life.
Results.— On average, patients equated living 1 year in their current state of
health with living 9.7 months in excellent health (mean [SD] utility, 0.81
[0.28]). Although only 126 patients (30.7%) rated their current quality of
life as excellent or very good, 284 (68.6%) were willing to give up at most
1 month of 12 in exchange for excellent health (utility ≥0.92). At the
other extreme, 25 (6.0%) were willing to live 2 weeks or less in excellent
health rather than 1 year in their current state of health (utility ≤0.04).
Patients were willing to trade significantly less time for a healthy life
than their surrogates assumed they would (mean difference, 0.05; P=.007); 61 surrogates (20.3%) underestimated the patient's time–trade-off
score by 0.25 (3 months of 12) or more. Patients willing to trade less time
for better health were more likely to want resuscitation and other measures
to extend life. Time–trade-off score correlated only modestly with quality-of-life
rating (r=0.28) and inversely with depression score
(r=−0.27), but there were few other clinical
or demographic predictors of health values. When patients who survived were
asked the time–trade-off question again at 1 year, they were willing
to trade less time for better health than at baseline (mean difference, 0.04; P=.04).
Conclusion.— Very old hospitalized patients who could be interviewed were able, in
most cases, to have their health values assessed using the time–trade-off
technique. Most patients were unwilling to trade much time for excellent health,
but preferences varied greatly. Because proxies and multivariable analyses
cannot gauge health values of elderly hospitalized patients accurately, health
values of the very old should be elicited directly from the patient.
LIFE EXPECTANCY has increased dramatically even among elderly adults
over the past few generations. Currently, an 80-year-old man can expect to
live 7 years and an 80-year-old woman, 9.1 years.1
But because the elderly disproportionately have both acute and chronic illnesses,
quality of life has assumed increasing importance.
There are 2 approaches to assessing health-related quality of life.
The health status approach describes functioning and well-being in 1 or more
domains, such as physical functioning, mental health, social function, role
function, pain, vitality, and health perception.2-5
Health status has been assessed in the elderly for over 30 years, most often
with measures of ability to perform activities of daily living (such as bathing,
dressing, eating, toileting, and transferring)6,7
and, increasingly, with brief, multidimensional surveys.3
The other approach to assessing health-related quality of life, known
as utility, preference, or value assessment, ascertains the desirability of
a state of health.2,8 One such health
value measure is the time trade-off, which quantifies a person's preference
for quality vs quantity of life. Health values are used in individual clinical
decision making as well as in health policy formulation.2,5,8,9
In clinical decision making, they can provide a general sense of how patients
feel about quality vs quantity of life, and they can be used in clinical decision
analyses to optimize treatment for an individual.2,10
Examples of using health values in clinical practice include helping couples
decide whether to have amniocentesis11 and deciding
when a patient with human immunodeficiency virus infection should start zidovudine
therapy.12 In addition, utility assessment has
demonstrated that clinical guidelines for management of ischemic heart disease
may not conform to preferences of affected patients.13
Utilities are most commonly used as quality-of-life adjustments to life
expectancy in the calculation of quality-adjusted life years (QALYs), which,
in turn, are used in clinical decision analyses and, in conjunction with cost
estimates, in cost-effectiveness (cost-utility) analyses. While many analysts8,14 advocate using QALYs for such purposes,
not all agree.15-17
La Puma and Lawlor16 have raised ethical concerns
over the use of QALYs in health policy formulation, one being that the "old-old"
cannot or will not provide health values and are thus disenfranchised.
Although much work has been done in geriatric health status assessment,
little is known about the health values of the very old. Health value assessment
in the elderly is particularly important because elderly patients receive
fewer invasive procedures and less resource-intensive hospital care than younger
patients, even when differences in severity of illness and preferences for
life-extending care are taken into account.18
Whether this different approach is with the assent of the patient or caregivers
is not clear. Given the importance of health values, if in fact health values
cannot be ascertained from frail elderly patients, it would be important to
know whether their health care proxies could provide accurate estimates or
whether health values can be predicted on the basis of health status or other
variables. Another important issue is whether health values change over time.
The Hospitalized Elderly Longitudinal Project (HELP) was a prospective
study of the prognoses, preferences, and decision making of hospitalized patients
aged 80 years or older, their surrogate decision makers, and their physicians.
The HELP study took place from January 1993 to November 1994 at 4 academic
medical centers (HELP was related closely to a concurrent study, the Study
to Understand Prognoses and Preferences for Outcomes and Risks of Treatments
project19). To qualify, patients had to be at
least 80 years old and hospitalized. Patients were excluded if they did not
speak English; were foreign nationals admitted specifically for a medical
procedure; had the acquired immunodeficiency syndrome (AIDS); had sustained
multiple trauma; were admitted for hospice care, to the psychiatry service,
or for an elective operation; were admitted to a hospital ward after transfer
from another hospital; died or were discharged within 72 hours of hospitalization;
or were scheduled for discharge within 72 hours of admission. For most patients,
a surrogate was identified.20
Interviews and Instruments
For each patient, severity of acute illness was ascertained using the
acute physiology score (APS) component of the Acute Physiology and Chronic
Health Evaluation III prognostic scoring system.21
Patients who were not intubated, were able to communicate, and were able to
pass a cognitive screening test22 were eligible
to be interviewed. Trained interviewers interviewed patients and surrogates
approximately 4 days and 12 months after study entry.
The health value measure used was the time–trade-off score.22-24 Patients and their surrogates
were independently asked in a systematic fashion whether the patient would
prefer living only 1 year in the patient's current state of health or less
time in excellent health, until an indifference point was ascertained. The
time–trade-off score was then calculated as the fraction of a year in
excellent health that was equivalent to a year of current health. For example,
if the patient were indifferent about choosing between living 12 months in
their current state of health or living only 9 months in excellent health,
their time–trade-off utility would equal 9 divided by 12 or 0.75. Possible
scores ranged from 0.04 (equivalent to indifference between 2 weeks in excellent
health and 1 year in current health) to 1.0. After the respondent completed
the time–trade-off question, the interviewer judged whether the respondent
understood the task; respondents who did not understand were excluded.
Health status instruments included (1) a global quality-of-life question,
in which the respondent was asked to rate the patient's quality of life as
excellent, very good, good, fair, or poor22;
(2) a revised measure of dependence in activities of daily living over the
previous 2 weeks6,22,25;
(3) a revised version of the Duke Activity Status Index,22,26,27
which assesses ability to perform strenuous activities; (4) a shortened version
of the Profile of Mood States,28,29
which assesses anxiety and depression; and (5) a measure of frequency and
severity of pain.19 In addition, we asked questions
concerning preferences regarding cardiopulmonary resuscitation (CPR); willingness
to tolerate each of 6 potentially lifelong adverse outcomes—pain, mechanical
ventilation, tube feeding, coma, confusion, and living in a nursing home;
preferences for care focused on extending life as much as possible, even if
it means having more pain and discomfort, vs care focused on relieving pain
and discomfort as much as possible, even if it means not living as long; and
perceived prognosis for surviving for 2 and 12 months and for functioning
independently in 2 and 12 months.22,30
We assessed the effect of the patient's illness on family members in terms
of assistance needed and savings depleted.28,31
For the Duke Activity Status Index, missing items were imputed from surrogate
responses for 5 patients.32
Means are expressed as mean (SD), and medians are given with 25th and
75th percentiles. Continuous variables were compared using the Wilcoxon rank
sum test. Within-patient changes over time were assessed with the Wilcoxon
signed rank test. Concordance between patients' and their surrogates' time–trade-off
scores was assessed using the Wilcoxon signed rank test. Univariate associations
between the time–trade-off and the health status measures, measures
of perceived prognosis, willingness to tolerate adverse outcomes, and demographic
variables were assessed using Spearman correlation coefficients.
Because time–trade-off scores were not normally distributed, we
used multivariable ordinal logistic regression to identify significant predictors
of time–trade-off scores at day 4 and month 12. Variables significantly
associated with time–trade-off scores in univariate analyses (when P<.10) and variables found to have been related to time–trade-off
scores in the Study to Understand Prognoses and Preferences for Outcomes and
Risks of Treatments study33 were entered into
the model and retained through backward elimination, if P was less than .05. A summary statistic for the ordinal logistic regression
models is Somers D, which measures the models' ability to predict time–trade-off
utilities. For a binary outcome (high vs low utilities) the statistic is a
linear function of the area under the receiver operating characteristic (ROC)
curve (D=2×[area under ROC−0.5]).
Within-patient changes in time–trade-off scores were compared
with changes in other measures using the Kruskal-Wallis test and Spearman
correlation coefficients. Analyses were performed using SAS statistical software
(SAS Institute, Inc, Cary, NC).
The HELP study enrolled 1266 patients. Many patients could not be interviewed:
25 patients (2.0%) were comatose or intubated or both; 272 (21.5%) were unable
to communicate for other reasons; 204 (16.1%) failed the cognitive screening
test; 29 (2.3%) died or were discharged within 72 hours; and 2 (0.2%) were
ineligible for other reasons. Of the 734 eligible for interview, 622 (84.7%)
participated. Of those 622, 62 (10.0%) terminated the interview before the
time–trade-off question was asked. Of the remaining 560 patients, 43
(7.7%) refused to answer the time–trade-off question, answered "don't
know," or had missing or incomplete answers. Of the 517 patients completing
the time–trade-off question at their initial interview, interviewers
provided judgments regarding the patient's understanding in 475 cases (91.9%);
414 (87.2%) were judged to have understood the task. Those 414 patients formed
our main analytic sample (Table 1).
In-hospital and 12-month mortality rates and APS scores were significantly
higher (higher APS scores indicate more severe illness) for the 852 excluded
patients than for the 414 who completed the time–trade-off question.
Among the 414 patients, 319 also had time–trade-off questions
completed by their surrogate at day 4. For the 319 surrogates' interviews,
interviewers' judgments regarding understanding of the time–trade-off
question were available for 311 (97.5%), and the interviewer believed that
300 (96.5%) of those surrogates understood the task. Compared with patients
who had a matching surrogate interview, patients without a surrogate interview
were similar in age, sex, and level of education attained and had similar
APS and Duke Activity Status Index scores but slightly more dependencies in
activities of daily living (1.08 vs 0.84 dependencies; P=.02). Of the patients alive at month 12, 176 (52%) completed and
understood a follow-up time–trade-off assessment.
The mean (SD) time–trade-off score for the 414 patients at their
initial interview was 0.81 (0.28) (median [25th, 75th percentile], 0.92 [0.83,
1.0]). This indicates that, on average, patients equated living 1 year in
their current state of health with living 9.7 months (0.81×12 months)
in excellent health. But time–trade-off scores varied widely from patient
to patient (Figure 1): 169 (40.8%)
had utilities of 1.0, meaning that they were unwilling to give up any time
in exchange for a shorter life in excellent health, and another 115 (27.8%)
had utilities of 0.92, meaning that they were willing to give up only 1 month
of 12 ([1-0.92]×12 months) in exchange for excellent health. Thus, more
than two thirds of the patients (284 [68.6%]) were willing to forgo at most
1 month of 12. At the other extreme, 25 (6.0%) had utilities of 0.04, indicating
that they preferred living 2 weeks or less in excellent health to living 1
year in their current state of health.
Patients Compared With Their Surrogates
Time–trade-off scores given by surrogates, who were asked to answer
as they thought the patient would, also varied widely. For the 300 patient-surrogate
pairs, the mean (SD) patient utility was 0.80 (0.30) (median [25th, 75th],
0.92 [0.83, 1.0]) and was higher than the mean surrogate utility by 0.05 (0.38)
(median difference, 0 [0, 0.17]; P=.007); 61 (20.3%)
of surrogates underestimated the patient's time–trade-off score by 0.25
(3 months of 12) or more. The correlation between patients' and their paired
surrogates' health values was modest (r=0.36).
Relationship of Heath Values to Other Measures
Time–trade-off utilities were related to patients' preferences
for CPR (Table 2). Patients who
desired CPR had a mean (SD) time–trade-off score at day 4 of 0.86 (0.23)
(median [25th, 75th], 0.92 [0.83, 1.0]);whereas, patients who preferred not
to undergo CPR had slightly lower mean scores of 0.75 (0.34) (median [25th,
75th], 0.92 [0.63, 1.0]; P<.001). Higher time–trade-off
scores were also related to patients' preferences for care that focused on
extending life: patients who preferred care that focused on extending life
had higher time–trade-off scores (ie, they were not willing to trade
away as much time) than patients who preferred care that focused on relieving
pain and discomfort.
Health values correlated only modestly (r=0.28)
with overall quality of life (Figure 2).
A total of 126 patients (30.7%) rated their current quality of life as excellent
or very good. For the patients with utilities of 1.0, indicating an unwillingness
to trade any time in current health for a shorter but healthier life, only
29 (17.3%) considered their quality of life to be excellent as is; 39 (23.2%)
rated it as very good, 61 (36.3%) as good, 32 (19.0%) as fair, and 7 (4.2%)
as poor. For the patients with utilities of 0.04 or less, 2 (8.0%) rated their
quality of life as excellent, 3 (12.0%) as very good, 6 (24.0%) as good, 3
(12.0%) as fair, and 11 (44.0%) as poor. Health values correlated modestly
(and inversely) with level of depression (r=−0.27);
but they correlated poorly if at all with other health status measures, willingness
to tolerate the 6 adverse outcomes, and perceived prognosis for survival and
independent functioning (Table 3).
Among the demographic variables, time–trade-off scores were not related
to age, sex, race, or level of education. In a multivariable analysis, on
average, patients who preferred treatment that extended life were more likely
to report high time–trade-off scores (odds ratio [OR], 2.8; 95% confidence
interval [CI], 1.8-4.4); in addition, health values were positively related
to quality of life (OR, 1.2 for each level of better quality of life; 95%
CI, 1.0-1.5) but were inversely related to level of depression (OR, 0.6 for
each level of more severely depressed mood; 95% CI, 0.4-0.7; Somers D=0.343).
Health Values 1 Year Later
For the 176 patients who completed the time–trade-off questions
at both day 4 and month 12, scores increased over the year by an average of
0.04, from 0.84 to 0.88 (SD of change, 0.30; median, 0; 25th percentile, −0.08;
75th percentile, 0.08; P=.04). This means that, a
year after hospitalization, on average, the time patients would give up in
their current state of health to be able to be in excellent health had declined
by 2 weeks. As at the initial interview, time–trade-off scores were
higher among those who desired CPR and among those who preferred life prolongation
over relief of pain and discomfort (Table
2); utilities were not significantly related to the degree of impact
of the illness on the family. At the 12-month interview, 60 patients (34.5%)
rated their quality of life as excellent or very good, but time–trade-off
scores correlated only moderately (r=0.24) with quality
of life. In a multivariable analysis, on average, patients who preferred treatment
that extended life were more likely to report high time–trade-off scores
(OR, 4.6; 95% CI, 2.1-10.0). Time–trade-off scores were positively related
to quality of life (OR, 1.6 for each level of better quality of life; 95%
CI, 1.2-2.1; Somers D=0.378). Change in time–trade-off scores was weakly
correlated with changes in quality of life, physiologic reserve, and mental
health (r=0.13-0.21).
Would an elderly person who is frail and ill prefer living as long as
possible over a shorter but healthy life? This study ascertained the health
values vis-à-vis quantity vs quality of life of a cohort of 414 hospitalized
patients aged 80 to 98 years. On average, patients indicated a fairly strong
"will to live": 40.8% were unwilling to exchange any time in their current
state of health for a shorter life in excellent health, and 27.8% were willing
to give up at most 1 month of 12 in return for excellent health. The variance
was large, however, with 6.0% of patients willing to live 2 weeks or less
in excellent health rather than 1 year in their current state of health. One
year later, surviving patients who could be interviewed had higher utilities
than during the index hospitalization, but again there was widespread variation.
The matter of how elderly patients weigh quantity and quality of life,
then, is highly individualistic. Importantly, our study demonstrated that
the majority of patients who could be interviewed understood and completed
the task at hand. This finding, coupled with the findings that surrogates
could not accurately gauge patients' health values and that health values
could not be predicted from demographic or clinical variables, signifies that,
when possible, health values should be ascertained directly from patients.
We are unaware of other studies of time–trade-off utilities focusing
solely on hospitalized very old patients. In the Beaver Dam Health Outcomes
Study, mean time–trade-off scores for patients older than 75 years with
any of a variety of chronic conditions were very similar (0.79-0.84, depending
on age and sex) to those we report (mean, 0.81); wide individual-to-individual
variation in utilities was also seen.34 Compared
with previously studied younger patients, the mean time–trade-off utility
of our elderly cohort was slightly lower than that of survivors of myocardial
infarction (0.87)35 and slightly higher than
that of patients with the acquired immunodeficiency syndrome (0.79)36 and of seriously ill patients (0.73).33
The findings that time–trade-off scores do not correlate well with health
status,13,36-39
are higher than surrogates believe,33 and increase
over time33 are by no means unique to the current
study, however.
There are several possible explanations for the abundance of high time–trade-off
scores. First, patients may have been unwilling to trade much time for "excellent
health" because they thought that their health was excellent at the time;
yet, when asked directly, only 13.2% rated it as excellent, and only 17.3%
of patients with utilities of 1.0 rated their health as excellent. Second,
we used a short time horizon (1 year) in the time–trade-off scenarios.
It is possible that, if presented with a longer life expectancy in current
health, patients would be willing to trade away a larger proportion for a
shorter but healthy life. Also, the sequence of the time–trade-off questions
or noise in the instrument could have affected the results.40
Further study of such issues and of other health value measures8
in elderly patients, sick or healthy, is warranted.
Findings from this study are relevant for decision making in both clinical
practice and policy making.2,5,10,13
For decision making at the individual patient level, time–trade-off
utilities can be used in a general sense to gauge the patient's "will to live"
or, more precisely, as quality-of-life weights in calculating QALYs for use
in decision analyses assessing the risks and benefits of various diagnostic
or therapeutic options.2,11,41,42
For decisions involving the allocation of health care resources, QALYs form
the denominator of cost-effectiveness (cost-utility) analyses for calculating
the incremental costs per incremental QALY gained for various programs, which
may in turn be compared with each other.2,14
But we should be cautious about promulgating health policy that neglects to
incorporate the wishes of individual patients. A recent study of patients
with angina by Nease and colleagues13 that also
found wide interpatient variation in health values (for their angina) concluded
that guidelines for managing ischemic heart disease should be based on individual
patients' preferences rather than symptom severity. Similarly, with wide variation
in the health values of the very old, there is a risk that guidelines developed
for their care will not conform to their preferences.
In summary, health values, as measured by the time trade-off, of very
old hospitalized patients who can be interviewed (1) can be elicited in most
cases; (2) indicate that patients are unwilling to trade much time in their
current health state for excellent health; (3) correlate with few other measures;
(4) are higher than surrogates believe; and (5) rise over 1 year among surviving
patients who could be reinterviewed. Because health values vary from patient
to patient, when possible, health values should be ascertained directly from
the patient.
1.Manton KG, Vaupel JW. Survival after the age of 80 in the United States, Sweden, France,
England, and Japan.
N Engl J Med.1995;333:1232-1235.Google Scholar 2.Tsevat J, Weeks JC, Guadagnoli E.
et al. Using health-related quality of life information: clinical
encounters, clinical trials, and health policy.
J Gen Intern Med.1994;9:576-582.Google Scholar 3.Ware Jr JE, Kosinski M, Keller SD. A 12-item short-form health survey: construction of scales and preliminary
tests of reliability and validity.
Med Care.1996;34:220-233.Google Scholar 4.Bergner M. Quality of life, health status, and clinical research.
Med Care.1989;27(suppl):S148-S156.Google Scholar 5.Patrick DL, Erickson P. Health Status and Health Policy: Quality of Life in Health Care
Evaluation and Resource Allocation. New York, NY: Oxford University Press; 1992.
6.Katz S, Ford AB, Moskowitz RW, Jackson BA, Jaffe MW. Studies of illness in the aged: the index of ADL: a standard measure
of biological and psychosocial function.
JAMA.1963;185:914-919.Google Scholar 7.Stuck AE, Aronow HU, Steiner A.
et al. A trial of annual in-home comprehensive geriatric assessments for elderly
people living in the community.
N Engl J Med.1995;333:1184-1189.Google Scholar 8.Torrance GW, Feeny D. Utilities and quality-adjusted life years.
Int J Technol Assess Health Care.1989;5:559-575.Google Scholar 9.Guyatt GH, Naylor CD, Juniper S, Heyland DK, Jaeschke R, Cook DJ.The Evidence-Based Medicine Working Group. Users' guide to the medical literature, XII: how to use articles about
health-related quality of life.
JAMA.1997;277:1232-1237.Google Scholar 10.Kassirer JP. Incorporating patients' preferences into medical decisions.
N Engl J Med.1994;330:1895-1896.Google Scholar 11.Pauker SP, Pauker SG. The amniocentesis decision: ten years of decision analytic experience.
Birth Defects.1987;23:151-169.Google Scholar 12.Lenderking WR, Gelber RD, Cotton DJ.
et al. Evaluation of the quality of life associated with zidovudine treatment
in asymptomatic human immunodeficiency virus infection.
N Engl J Med.1994;330:738-743.Google Scholar 13.Nease Jr RF, Kneeland T, O'Connor GT.
et al. Variation in patient utilities for outcomes of the management of chronic
stable angina: implications for clinical practice guidelines.
JAMA.1995;273:1185-1190.Google Scholar 14.Gold MR, Siegel JE, Russell LB, Weinstein MC. Cost-effectiveness in Health and Medicine. New York, NY: Oxford University Press; 1996.
15.Kolata G. Ethicists struggle to judge the ‘value' of life.
New York Times.November 24, 1992:C3.Google Scholar 16.La Puma J, Lawlor EF. Quality-adjusted life-years: ethical implications for physicians and
policymakers.
JAMA.1990;263:2917-2921.Google Scholar 17.Hadorn DC. Setting health care priorities in Oregon: cost-effectiveness meets
the rule of rescue.
JAMA.1991;265:2218-2225.Google Scholar 18.Hamel MB, Phillips RS, Teno JM.
et al. Seriously ill hospitalized adults: do we spend less on older patients?
J Am Geriatr Soc.1996;44:1043-1048.Google Scholar 19.The Writing Group for the SUPPORT Investigators. A controlled trial to improve care for seriously ill hospitalized adults:
the Study to Understand Prognoses and Preferences for Outcomes and Risks of
Treatments (SUPPORT).
JAMA.1995;274:1591-1598.Google Scholar 20.Murphy DJ, Knaus WA, Lynn J. Study population in SUPPORT: patients (as defined by disease categories
and mortality projections), surrogates, and physicians.
J Clin Epidemiol.1990;43(suppl):11S-28S.Google Scholar 21.Knaus WA, Wagner DP, Draper EA.
et al. The APACHE III prognostic system: risk prediction of hospital mortality
for critically ill hospitalized adults.
Chest.1991;100:1619-1636.Google Scholar 23.Torrance GW, Thomas WH, Sackett DL. A utility maximization model for evaluation of health care programs.
Health Serv Res.1972;7:118-133.Google Scholar 24.Tsevat J, Dawson NV, Matchar DB. Assessing quality of life and preferences in the seriously ill using
utility theory.
J Clin Epidemiol.1990;43(suppl):73S-77S.Google Scholar 25.Landefeld CS, Phillips RS, Bergner M. Patient characteristics in SUPPORT: functional status.
J Clin Epidemiol.1990;43(suppl):37S-39S.Google Scholar 26.Phillips RS, Goldman L, Bergner M. Patient characteristics in SUPPORT: activity status and cognitive function.
J Clin Epidemiol.1990;43(suppl):33S-36S.Google Scholar 27.Hlatky MA, Boineau RE, Higginbotham MB.
et al. A brief self-administered questionnaire to determine functional capacity
(the Duke Activity Status Index).
Am J Cardiol.1989;64:651-654.Google Scholar 28.Oye RK, Landefeld CS, Jayes RL. Outcomes in SUPPORT.
J Clin Epidemiol.1990;43(suppl):83S-88S.Google Scholar 29.Shacham S. A shortened version of the Profile of Mood States.
J Pers Assess.1983;47:305-306.Google Scholar 30.Coulton CJ. Decision making in SUPPORT: patient perceptions and preferences.
J Clin Epidemiol.1990;43(suppl):51S-54S.Google Scholar 31.Covinsky KE, Goldman L, Cook EF.
et al. The impact of serious illness on patients' families.
JAMA.1994;272:1839-1844.Google Scholar 32.Wu AW, Damiano AM, Lynn J.
et al. Predicting future functional status for seriously ill hospitalized
adults: the SUPPORT prognostic model.
Ann Intern Med.1995;122:342-350.Google Scholar 33.Tsevat J, Cook EF, Green ML.
et al. Health values of the seriously ill.
Ann Intern Med.1995;122:514-520.Google Scholar 34.Fryback DG, Dasbach EJ, Klein R.
et al. The Beaver Dam Health Outcomes Study: initial catalog of health-state
quality factors.
Med Decis Making.1993;13:89-102.Google Scholar 35.Tsevat J, Goldman L, Lamas GA.
et al. Functional status versus utilities in survivors of myocardial infarction.
Med Care.1991;29:1153-1159.Google Scholar 36.Tsevat J, Solzan JG, Kuntz KM.
et al. Health values of patients infected with human immunodeficiency virus:
relationship to mental health and physical functioning.
Med Care.1996;34:44-57.Google Scholar 37.Llewellyn-Thomas HA, Sutherland HJ, Tritchler DL.
et al. Benign and malignant breast disease: the relationship between women's
health status and health values.
Med Decis Making.1991;11:180-188.Google Scholar 38.Revicki DA. Relationship between health utility and psychometric health status
measures.
Med Care.1992;30(suppl):MS274-MS282.Google Scholar 39.Bosch JL, Hunink MGM. The relationship between descriptive and valuational quality-of-life
measures in patients with intermittent claudication.
Med Decis Making.1996;16:217-225.Google Scholar 40.Froberg DG, Kane RL. Methodology for measuring health-state preferences, III: population
and context effects.
J Clin Epidemiol.1989;42:585-592.Google Scholar 41.Plante DA, Kassirer JP, Zarin DA, Pauker SG. Clinical decision consultation service.
Am J Med.1986;80:1169-1176.Google Scholar 42.Weinstein MC, Fineberg HV. Clinical Decision Analysis. Philadelphia, Pa: WB Saunders Co; 1980.