Here - American Geriatrics Society
Here - American Geriatrics Society
Here - American Geriatrics Society
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P OSTER<br />
A BSTRACTS<br />
the use of instruments validated for this particular environment is not<br />
yet widespread. The ideal timing of or interval during which a delirium<br />
screening process should take place has yet to be determined. Future<br />
research in the ED will be needed to both validate delirium<br />
screening instruments that are currently used for investigation and<br />
clinical care as well as to define the ideal timing and form of the delirium<br />
assessment process for older adults.<br />
B30<br />
Pain Care in the Emergency Department: Is it Satisfactory?<br />
M. Barlow, U. Hwang. Department of Emergency Medicine;<br />
Department of <strong>Geriatrics</strong> and Palliative Medicine, Mount Sinai<br />
School of Medicine, New York, NY.<br />
Supported By: Michelle Barlow was funded by an AFAR grant<br />
through the 2011 MSTAR program.<br />
Ula Hwang is supported by a K23 award from the NIA.<br />
BACKGROUND: Pain is a common reason for emergency department<br />
(ED) visits by older adults. There is evidence that older<br />
adults receive poorer ED pain care than younger patients, but many<br />
of these studies used retrospective data and were unable to assess patient<br />
satisfaction. The objective of this study is to compare the quality<br />
of ED pain care received with patient satisfaction.<br />
METHODS: This is a prospective observational study at an academic,<br />
tertiary care medical center that has been ongoing since July<br />
2011. Adult patients (≥ 20 years), who present to the ED with severe<br />
abdominal pain (pain score 10 out of 10) are surveyed at the end of<br />
their ED visit regarding their pain, care received, and satisfaction levels.<br />
Quality metrics of pain care received as well as covariates (age,<br />
gender, ethnicity, Charlson comorbidity score, etc.) are abstracted<br />
from the medical record.<br />
RESULTS: Between July 7 and November 14, 2011, 90 subjects<br />
meeting inclusion criteria were surveyed. There were no significant<br />
differences between older adults (65+ years, 16%) and younger<br />
adults (20-64 years, 84%) in their surveyed pain scores, time to first<br />
analgesic administration, nor overall receipt of analgesics. There was<br />
also no difference in pain care satisfaction. When comparing the 69%<br />
of patients satisfied with pain care versus the 31% who were unsatisfied,<br />
those who were satisfied had lower surveyed pain scores (5.64 vs.<br />
8.88, p < 0.0001) and were less likely to want more analgesics (37% vs.<br />
86%, p < 0.0001). Unsatisfied patients waited longer for administration<br />
of first analgesic (trend, p = 0.09). There was, however, no significant<br />
difference in analgesic administration (86% of unsatisfied received<br />
analgesics vs. 85% of satisfied).<br />
CONCLUSIONS: Pain care satisfaction is associated with lower<br />
pain scores and decreased desire for additional analgesics. Contrary<br />
to growing evidence of poorer ED pain care for older adults, subjects<br />
in this cohort appear to receive equivalent care to their younger<br />
counterparts. Older and younger adults received and had analgesics<br />
administered in similar time frames; they also had similar pain scores<br />
and levels of satisfaction. This is the opposite of recent studies and<br />
may indicate that both the type (abdominal versus other pain) and<br />
severity of pain described as well as the quality indicators used to define<br />
appropriate care may impact the level of discrepancy observed.<br />
B31<br />
Functional Impairment and Disability during the Last Two Years<br />
of Life.<br />
A. K. Smith,Y. Miao,W. Boscardin, K. Covinsky. Medicine, Division of<br />
<strong>Geriatrics</strong>, University of California, San Francisco, San Francisco, CA.<br />
Supported By: NIA, NCRR.<br />
Background: We know little about the national prevalence of<br />
disability at varying points across the last years of life.<br />
Methods: Data are from participants ages 50+ who died in the<br />
Health and Retirement Study (HRS) between the years 1995 and<br />
2008. Each participant was interviewed once in the last 24 months of<br />
life. We used the HRS interview closest to death to reconstruct national<br />
estimates of the monthly prevalence of functional impairment<br />
and disability in the two years prior to death. Measures of functional<br />
impairment and disability included: IADL difficulty (Difficulty with<br />
cooking, shopping, using telephone, taking medications, managing<br />
money); ADL dependence (requires assistance with dressing,<br />
bathing, eating, transferring, walking across the room, and toileting).<br />
We estimated the predicted probability of functional impairment or<br />
disability by age at death and gender, adjusting for race or ethnicity,<br />
educational level, net worth, and proxy status.<br />
Results: There were 7624 decedents (mean age at death 80,<br />
52%% women, 84% White, 10% African-<strong>American</strong>, 4% Latino, 27%<br />
proxy interview). The unadjusted prevalence of all forms of functional<br />
impairment rose linearly over the last two years of life (Table).<br />
The predicted prevalence of disability prior to death rose with advancing<br />
age. After adjustment for gender, race/ethnicity, educational<br />
level, net worth, and proxy status, the predicted prevalence of any<br />
ADL dependency for elders ages 50-69 12 months prior to death was<br />
24% (95% CI 18-29), compared to 29% (24-34) for ages 70 to 79, 37%<br />
(31-44) for ages 80 to 89, and 47% (41-54) for ages 90 and older (p for<br />
trend