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Late-breaking abstracts / European Geriatric Medicine 6S1 (2015) S177

S187

S185

most important, followed by the disease severity, and discussion

with health care professionals. However, despite incurable diseases

and terminal conditions, 12(40.0%) patients would follow the advice

by doctors, 9(30%) wished to go home, and 5(16.7%) agreed hospice

care. ADs would be considered if life expectancy is less than 3

months in 16(53.3%) patients, 4 to 12 months in 6(20%), but

7(23.3%) would never consider ADs. Patients who were married,

high school educated, and their spouse as the main caregiver had

higher awareness of ADs. Attitude was positive among patients

with APACHE II scores ≥16 and spouse as the main caregiver.

Conclusion:

Discussion and advice of medical professionals played

an important role in decision of ADs. Education to medical

professionals and patients might be of help.

P-480

Does obesity really lower dementia risk?

B.H. Strand

1

, E. Langballe

2

, T.A. Rosness

3

, K. Engedal

4

, E. Bjertness

3

1

Norwegian Institute of Public Health/University of Oslo, Oslo,

Norway;

2

Aldring og Helse, Tønsberg, Norway;

3

University of Oslo,

Oslo, Norway;

4

Nasjonalt Kompetansesenter for Aldring og Helse, Oslo,

Norway

Objectives:

A paper by Qizilbash et al., published in Lancet Diabetes

and Endocrinology in April this year, reported that underweight in

midlife increases dementia risk, and contrasting previous research

they reported that overweight in midlife lowers dementia risk. This

study has been questioned because they considered individuals

between 40–80 years of age at BMI assessment as a single group,

mixing midlife and late-life BMI.

Methods:

For this reason, we analyzed separately the dementia risk

for three age groups at BMI assessment: 35–49, 50–69 and 70–80

years. Our data includes more than 80 000 participants in Norway

followed-up for dementia related mortality, using Cox regression,

with a maximum of 38 years of follow-up.

Results:

Two aspects of our findings need to be considered.

First, underweight both in midlife and old age was associated

with increased dementia risk. Second, the association between

overweight and dementia depended on age at BMI assessment;

when BMI was assessed in midlife there was no decreased dementia

risk, but when BMI was assessed in old age, high BMI was associated

with decreased dementia risk.

Conclusions:

Obesity involves increased health risk for several

conditions. Based on the Qizilbash paper, global news corporations

have reported that being overweight in midlife may reduce

the risk of dementia. We believe the uncertainties concerning

clinical relevance of the Qizibalsh paper findings should be noted,

particularly that other studies find no such protective effect of

midlife overweight. However, being underweight at different stages

in life seems to be associated with increased dementia risk. To gain

more knowledge about the associations between weight, dementia

and the mechanisms involved, further investigation is warranted.

P-481

Assessment and treatment of memory problems in memory

clinic setting: A study of 60 patients

N. Ahmad

1

1

Queens Hospital, Romford, United Kingdom

Aims:

To analyse the clinical assessment, diagnosis and treatment of

patients presenting with memory problems in the memory clinic

Patients and Methods:

60 consecutive patients case notes were

audited who presented to memory clinic from Jan to July 2010.

Their clinical assessment, investigations and treatment options

were noted and their mini-mental score was charted over two

years.

Results:

Patients treated with choline esterase inhibitors showed

stable MMSE over a period of two years whereas the patients who

were not treated (for variety of reasons) continue to deteriorate

rapidly.

Discussion and Results:

Treatment with anti-dementia drugs can

provide a good quality of life for elderly patients up-to a period of

two years.

P-482

The Norwegian Cognitive Impairment After Stroke study

(Nor-COAST)

I. Saltvedt

1

, T. Askim

1

, B. Indredavik

1

, T. Engstad

2

, H. Næss

3

,

H. Ihle-Hansen

4

, B. Fure

5

, M. Beyer

6

1

Norwegian University of Science and Technology (NTNU), Trondheim,

Norway;

2

University Hospital of North Norway, Tromsø, Norway;

3

Haukeland University Hospital, Bergen, Norway;

4

Vestre Viken,

Bærum Sykehus, Høvik, Norway;

5

Ullevaal University Hospital, Oslo,

Norway;

6

Oslo University Hospital, Oslo, Norway

Objectives:

After stroke more than 50 percent of the patients get

post-stroke dementia (PSD) or mild cognitive impairment (MCI).

This is an exponentially increasing patient population due to ageing

of population and decreased mortality among stroke patients. The

overall aim of The Norwegian Cognitive Impairment After Stroke

(Nor-COAST) study is to establish a research platform that will

improve competence on PSD and MCI in order to improve individual

health outcomes following a stroke.

Methods:

Nor-COAST is an ongoing descriptive cohort study with

partners from all four Norwegian health authorities. Up to 1000

patients with acute stroke admitted to one of the six participating

stroke units will be included. Data collection at baseline, discharge

from hospital, at 3 and 18 months include evaluation of cognition,

life style, physical activity, function, MRI, blood samples, activity

monitoring (active PAL), and data on pharmacological and non-

pharmacological secondary prevention.

Results:

Nor-COAST will give increased knowledge on the following

aspects of PSD / MCI: i) incidence and clinical phenotype ii)

pathogenetic factors including MRI, biomarkers and genetics

iii) importance of physical activity iv) the interaction between

secondary prevention and development of PSD/MCI v) clinical

methods that can identify risk patients.

Conclusion:

Cognitive impairment after stroke is frequently

overlooked, and we think that this study will increase competence,

and that the results obtained can be used both in clinical care and

later intervention studies.

P-483

Clinical trial for the evaluation of an adaptive robotic gait

rehabilitation system with geriatric patients

F. Feldwieser

1

, B. Wagner

1

, E. Steinhagen-Thiessen

2

1

Geriatrics Research Group, Department of Geriatric Medicine,

Charit´e

Universit¨atsmedizin Berlin, Berlin, Germany;

2

Research

Group on Geriatrics, Charit´e

Universit¨atsmedizin Berlin, Berlin,

Germany

Objectives:

The scarcity of resources in the healthcare sector

calls for alternative ways of treatment and interventions. Robotic

gait assistance systems which can be adapted to the patient’s

anatomy are one possible alternative. Project MOPASS developed

an intelligent and adaptive system for gait rehabilitation which

can help patients to train physiological gait patterns by the

provision of constant feedback to the patient. This helps to

substitute unphysiological gait patterns with more physiological

gait patterns. Additionally new therapeutic treatment intervention

will be created.

Methods:

Within a clinical trail the usability and acceptance of

the mobile robotic assisted gait rehabilitation system MOPASS was

tested from the perspective of ten geriatric patients and three

physiotherapists. Data was collected with the help of questionnaires

and guided interviews. Information on wearing comfort, operability