MEDICATION MANAGEMENT IN OLDER ADULTS
M551
of the evaluation, including PRN or “as needed” medica-
tions, using the DRUGS tool. A visual aid, in the form of a
sheet of paper marked with a grid labeled “time” (7 am–11
pm), “meal,” and “medications,” is employed to standardize
the process. The DRUGS tool is an easy-to-administer indi-
vidualized measure that examines medication self-adminis-
tration. It takes approximately 4 to 5 minutes, and interrater
and test-retest reliability of the DRUGS tool are Ͼ.90 (11).
The Spearman correlation, Fisher’s exact, chi-square, and
Wilcoxon rank sum tests were employed to examine the re-
lationships between predictors.
New variables were derived to control for baseline values
by calculating the mathematical difference between values
at either 6 or 12 months and baseline values. Multivariate
models were derived using stepwise linear regression in
which the dependent variable was either baseline DRUGS
summary score or 6- or 12-month change in DRUGS sum-
mary score. Age, sex, and covariates with p Ͻ .2 on univari-
ate analysis were entered into the models, and variables
with p Ͻ .05 were retained in the models. Additional statis-
tical analyses were performed to explore whether changes
in self-reported medication management capacity or MMSE
were also associated with the standard measures or clinical
outcomes. Stepwise logistic regression models were derived
using baseline self-reported medication management capac-
ity as the dependent variable. Collinearity diagnostics were
performed on the final models. Nonsignificant predictors
were entered into the final models to check for uncontrolled
confounding (change in  coefficient of Ͼ10%). Residual
and regression diagnostics were performed.
Standard Measures of Functional Status
The results of these geriatric screening tools were com-
pared with a complement of previously validated standard
measures of functional status, which were categorized for
clinical relevance. There were tests of cognitive status
(Mini-Mental State Examination [MMSE]), affective status
(15-item Geriatric Depression Scale), physical function
(timed “Up and Go” test), medical conditions (Jaeger card to
test near vision, Charlson Comorbidity Index), medication-
specific factors (number of medications, number of doses),
and social factors (living alone or with a partner) (14–18).
Covariates included age, gender, and level of education.
Patients and Setting
RESULTS
This prospective cohort study was conducted at two con-
tinuing-care retirement facilities in the greater Boston area.
Patients were recruited from the Beth Israel Deaconess Ger-
ontology Group practice between October 10, 1996, and Jan-
uary 27, 1997. All ambulatory community-dwelling patients
aged 70 years and older who presented to one of the study
sites were eligible for the study. Patients were excluded if
they were currently not taking any prescription or nonpre-
scription medications or if they refused to participate.
Study Population
A total of 67 patients were approached. Four were ineligi-
ble, two did not take any medications, one lived in a differ-
ent facility at the time of the study, and five declined to par-
ticipate (these individuals were more cognitively and
functionally impaired than those who agreed to participate).
A total of 58 subjects were enrolled in the study and com-
pleted the baseline assessment. At 6 months, three patients
had moved from independent apartments to an on-site
skilled nursing facility (study endpoint). Fifty-three of the
55 community-dwelling patients (96%) completed the
6-month follow-up assessment; one refused to participate
and another did not complete the DRUGS test. Forty-seven
(86%) of the 55 eligible participants completed the 12-
month follow-up assessment; five refused to complete the
study, and three were lost to follow-up.
The mean age at study entry was 84.2 Ϯ 5.1 years; 72%
of the participants were women, 68% were college edu-
cated. There was no significant difference between the
patients who participated in the baseline, 6-month, and 12-
month assessments in terms of age, gender, living arrange-
ment, or level of education (Table 1).
Data Collection
Data for all participants were collected at the time of the
initial outpatient office visit (HE, ES) and at a 6-month fol-
low-up visit. The initial contact was used to obtain written
informed consent and collect clinical data. The chart review
data included the list of medications and the 19 variables
that constitute the Charlson Comorbidity Index (18). Test
status was ascertained by an investigator (HE, ES) who was
blinded to health status and sociodemographic factors. An
additional office visit was scheduled at 6 months. Data were
obtained regarding predefined clinical outcomes: interim
clinic visits (0, Ն2), emergency room visits (0, Ն1), acute
care hospitalizations (0, Ն1), institutionalization, and death.
This information was confirmed by chart review. The insti-
tutional review board of the Beth Israel Deaconess Medical
Center approved the protocol.
Table 1. Demographic Data at Baseline, 6, and 12 Months
Data Analysis
Baseline
6 Mo
12 Mo
Univariate and multivariate analyses were performed us-
ing the SAS statistical package for Windows, version 6.12
(SAS Institute Inc., Carey, NC). Univariate associations be-
tween the continuous outcomes (DRUGS summary score,
change in DRUGS summary score) and continuous vari-
ables were examined by Spearman correlation. Student’s t
test was used to compare the DRUGS score and change in
DRUGS score between two groups for binary predictors.
Bonferroni correction was applied to multiple comparisons.
Number of participants (%)
Mean age, y (SD)
Gender, number women (%)
Living arrangement, number
alone (%)
Level of education, number
completed college (%)
Assisted living, number (%)
Nursing home, number (%)
59
84.2 (5.1)
43 (72)
53 (90)
84.1 (4.9)
37 (70)
47 (81)
85.2 (5.3)
31 (70)
44 (73)
37 (70)
31 (70)
41 (69)
3 (5)
0 (0)
36 (68)
5 (8)
3 (5)
30 (4)
9 (18)
3 (6)