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Oral presentations / European Geriatric Medicine 5S1 (2014) S45–S81 S61
Figure: The proportion of available and applicable information.
O2.18
The development of the Appropriate Psychotropic drugs use
In Dementia (APID) index
K. van der Spek1, D.L. Gerritsen1, S.U. Zuidema2,
M.H.J.M.G. Nelissen-Vrancke3, R.B. Wetzels1, C.H.W. Smeets1,
M. Smalbrugge4, R.T.C.M. Koopmans1
1Radboudumc, Nijmegen, The Netherlands; 2University Medical Center
Groningen, Groningen, The Netherlands; 3Dutch Institute for Rational
Use of Medicine, Utrecht, The Netherlands; 4VU Medical Center,
Amsterdam, The Netherlands
Introduction: There are many tools to measure appropriate drug
use, but these, including the Medication Appropriateness Index
(MAI), are not specified for psychotropic drug use (PDU) for
neuropsychiatric symptoms (NPS) in dementia. For this purpose,
the MAI needs to be adjusted, by developing an index with relevant
items that weighs drug use against specific guidelines. The aim of
this study is to develop an index derived from the MAI items that
is suited for research in PDU for NPS in dementia and to test its
reliability and validity.
Methods: An expert panel used the MAI items to construct items
for appropriateness in PDU; a second independent expert panel
validated this process, to create the APID index. An inter-rater
reliability study was conducted and an index’ summated score was
developed to enhance the use in clinical studies. Construct validity
was explored using a sample of 560 medical files.
Results: Five existing and one adjusted MAI items were used, the
item ‘evaluation’ was added. The second expert panel concluded
that all items contributed to the construct. All items and the
index’ summated score had moderate to almost perfect inter-
rater reliability. The index’ summated score reflects putative
distribution.
Conclusions: The results of this study show that the APID items
are reliable and valid for measuring appropriateness of PDU in
dementia. The index’ summated score is reliable and valid for use
in clinical studies.
O2.19
Are drugs with sedative properties a risk factor for oral health
habits in community-dwelling older people?
A.T. Tiisanoja1, A.M. Syrjala1, K. Komulainen2, S. Hartikainen2,
H. Taipale2, M. Knuuttila1, P. Ylostalo2
1University of Oulu, Oulu, Finland; 2University of Eastern Finland,
Kuopio, Finland
Introduction: Because of the high consumption of drugs with
sedative properties, it is important to study the effects of these
drugs on oral health habits among older population. The aim was
to study whether sedative load, which measures the cumulative
effect of taking multiple drugs with sedative properties, is related
to oral health habits, such as toothbrushing, using toothpaste, dental
visits and number of teeth with dental plaque, among community-
dwelling older people.
Methods: The study population consisted of 159 (112 women and
47 men, mean age 79.3 years) community-dwelling, dentate, non-
smoking, older people from the Geriatric Multidisciplinary Strategy
for the Good Care of Older People study. The data were collected by
interviews and clinical examinations during 2004–2005. Sedative
load (SL) was calculated using the Sedative Load Model. Logistic and
Poisson regression models were used to estimate odds ratios (OR)/
relative risks (RR) and 95% confidence intervals (CI).
Results: After adjusting for confounding factors, both moderate
(1–2) and high (≥3) sedative load were associated, although not
strongly, with toothbrushing (SL 1–2: OR 1.29, CI 0.38–4.41) and
using toothpaste (SL ≥3: OR 4.52, CI 0.84–24.4) less than twice a day,
irregular dental visits (SL 1–2: OR 1.75, CI 0.69–4.59) and higher
number of teeth with dental plaque (SL ≥3: RR 1.10; CI 0.94–1.29).
Conclusions: Within the limitations of this study, including small
sample size, the results suggest that the use of drugs with sedative
properties is a potential risk factor for poor oral health habits.
O2.20
Effects of clinical pharmaceutical counseling on medication
safety in geriatric patients
A. de Campo1, I. Friedl2, W. Schippinger1
1Geriatic Health Centers, Graz, Austria; 2LKH Graz West, Graz, Austria
Introduction: To warrant the safety of drug therapy is always
challenging, especially so when treating geriatric patients with
frailty or high comorbidity, who often need extensive drug therapy.
The present study aims to evaluate if comprehensive counseling of
prescribing physicians, nursing staff and patients done by a clinical
pharmacist leads to measureable effects in regard to occurrence
and frequency of adverse drug reactions.
Methods: A randomized, controlled, prospective, open, parallel-
group design was chosen for a mono-center pilot study. 100
participants were enrolled.
As clinical parameters we chose laboratory results, ECG and
parameters of the Geriatric Assessment. Non-clinical parameters
were employed to assess the risk for adverse drug reactions. To
assess the appropriateness of medication prescriptions a synopsis
of tools was used: PIM (Potentially Inappropriate Medication) lists, a
dosing tool, product information and drug interactions data bases.
Results: Analysis of the clinical data showed significant differences
in renal parameters (D signifies the change from baseline to end of
study):
DCreatinine: −0.04±0.13 for the intervention group vs. 0.12±0.49
for the control group; p =0.047.
DUrea: −1.5±9.4 for the intervention group vs. 8.3±26.1 for the
control group; p =0.032.
The differences in non-clinical parameters at end of study were
pronounced: intervention group vs. control group number of drugs:
8.1% difference, PIMs 18.4% difference, dosing recommendations:
56.5% difference, drug interactions: 72.7% difference, all in favor of
the intervention group.
Conclusion: Our results suggest that comprehensive counselling
can improve medication safety.