Table of Contents Table of Contents
Previous Page  205 / 290 Next Page
Information
Show Menu
Previous Page 205 / 290 Next Page
Page Background

P-644

GNRI as a complement to MNA in nutrition study

M. Freixa, A. Simões, J. Rodrigues, S. Úria, G. Silva.

Department of

Internal Medicine, Pulido Valente Hospital, Lisbon, Portugal

Introduction:

Geriatric Nutritional Risk Index (GNRI) identify the risk

of nutrition-related complications in elderly. Malnutrition is common

in this population, higher in those hospitalized, and is frequently

evaluated by Mini Nutritional Assessement (MNA).

Objective:

Investigate the correlation between MNA and GNRI.

Methods:

Cross-sectional study with 66 hospitalized elderly patients

(

65 years) divided into two groups according to MNA-Short Form

G1 malnourished (

7; n = 11); G2 without malnutrition (>7). There

was also used anthropometric measures (bodymass index (BMI); mid-

arm muscle circumference (MUAMC)

71% severe, 70

80% moderate

and 80

90% mild nutrition) and albumin (normal

3 g/dL). GNRI: >98

no risk, 92

98 low, 92

82 moderate, <82 severe.

Results:

(1) Mean age was similar (82,2 ± 4.5 vs 83.1 ± 6.2 years;

p = 0.6). (2) G1 had lower mean MNA (5.3 ± 1.8 vs 11.9 ± 2.2; p < 0.01).

(3) G1 had lower BMI (20.05 ± 2.05 vs 25.1 ± 4.34; p < 0.01) and positive

relation with MUAMC in both groups (69,5 ± 9,3 vs 83,9 ± 14,02;

p < 0,01). (4) Higher prevalence of hypoalbuminaemia in G1 (45,5

vs 19,6%; p = 0,069). (5) Both groups had mean GNRI <98, but G1

had lowest value (80,7 ± 16,4 vs 96.72 ± 13.4; p < 0.01). (6) In G2, 15,4%

had GNRI <82 (vs 45,5%) and 9,6% between 82 and 92 (vs 27,3%;

p = 0,010).

Conclusion:

Some patients classified with no malnutrition may be

at risk to develop nutrition-related complications. It is essential to

determine the GNRI in hospitalized patients, predicting complications

and planning an effective nutritional intervention.

P-645

The metabolic syndrome in very elderly

M. Freixa, A. Simões, J. Rodrigues, S. Úria, G. Silva.

Department of

Internal Medicine, Pulido Valente Hospital, Lisbon, Portugal

Introduction:

The metabolic syndrome (MS) is defined as a cluster of

cardiometabolic risk factors, and elderly have highest prevalence.

However, few studies have directed attention to the MS in this

population.

Objective:

To evaluate metabolic syndrome in the elderly.

Methods:

A retrospective observational study with analysis of 144

clinical process of patients with MS, from admission in consultation to

the last clinical evaluation. Mean follow-up time was 5,7 ± 3,6 years.

SM was defined according to the AHA/NHLB2005 criteria. We defined

two groups: G1 <80 years (n = 123, 74,1%) and G2 > 80 years.

Results:

(1) In G1, males were superior (66,7 vs 42,9%;p = 0,050) while

in G2 was the female gender (57,1 vs 33,3%;p = 0,050). (2) The mean

age in G1 was 60,9 ± 10,4 years (vs 85 ± 3,8). (3) On admission, in G2

therewas a higher prevalence of dyslipidemia (100 vs 75,2%; p = 0,007),

hypertension (85,1 vs 71,4%; p = 0,127), chronic kidney disease (23,8

vs 8,3%;p = 0,05), heart failure (42,9 vs 20,7%; p = 0,049), ischemic

cardiopathy (33,3 vs 7,4%; p = 0,003), atrial fibrillation (42,9 vs 5,8%;

p < 0,001) and stroke (30 vs 8,9%; p = 0,016). (5) G2 hadworse LDL levels

(127,2 ± 85,6 vs 114,5 ± 43,1 mg/dL) and glycaemia (126,8 ± 56,1 vs

116,8 ± 42,9 mg/dL) but better triglycerides level (127,7 ± 121,5 vs

168,8 ± 127,9 mg/dL) and total colestherol (192,43 ± 48,4 vs 193,7 ±

52,2 mg/dL). In both groups, patients were overweight (BMI 30,4 ± 6,3

vs 29,6 ± 6,4). (6) During follow-up, G1 had developed more hepatic

steatosis (37,4 vs 4,8%;p = 0,002) and diabetes (20 vs 9,5%; p = 0,365).

(7) Mortality was higher in G2 (28,6vs9,8%; p = 0,027).

Conclusions:

In our study, the older people have more cardiovascular

risk factors, but the younger group developed more hepatic steatosis

and diabetes. MS is a risk factor for cardiovascular morbidity, whereby

it is important to diagnose and prevent its development.

P-646

Cross-sectional analysis of fasting blood glucose and cognition in

geriatric inpatients

M. Gogol.

Department of Geriatrics, Lindenbrunn Hospital,

Coppenbruegge, Germany

Background:

Diabetes mellitus affecting increasingly aging persons,

alters mirco- and macrocirculation and foster ateriosclerosis, which

play a role in accelerating aging and cognitive decline. Diabetes

nowadays is recognized as a metabolic and vascular risk factor for

cognitive decline including Alzheimer

s and vascular dementia.

Purpose:

To prove the hypothesis that diabetes mellitus is an

independent risk factor for cognitive decline.

Methods:

Geriatric inpatients were tested in a prospective, cross-

sectional design for cognition using the Mini Mental Status

Examination (MMSE, range 0

30 points, higher results inidcating

better cognitive function) and blood sugar day profiles. In accordance

to guidelines we used following cut-offs: normal fasting blood glucose

(NFG) < 100 mg%, impaired fasting blood glucose 100

125 mg%,

and elevated fasting blood glucose (EFG)

126 mg%. Pearson

s

correlation and Student

s t-test were used for statistical calculations,

p values were set to 0.05 or lower for significance.

Results:

We examined 478 consecutive geriatric inpatients with a

mean age of 78.89 ± 8.06 years (197 men (m), 77.23 ± 8.19, 287 women

(w) 81.71 ± 8.19, p = 0.000). NFG were detected in 171 (67 m, 104 w,

mean 91 ± 6.8 mg%), IFG in 208 (80 m, 128 w, mean 110.7 ± 7.3 mg%),

and EFG in 99 (49 m, 50 w, mean 153.1 ± 38.9 mg%) patients. Cognitive

testing with MMSE revealed mean scores of 22.93 ± 5.45

(m 23.25 ± 5.54, w 22.71 ± 5.39, p = 0.28). Total MMSE scores and

subscores for immediate and delayed recall as well as attention/

calculation task revealed no correlation with fasting blood glucose

levels. Pearson

s r for MMSE total was 0.0578 (m 0.0601, w 0.0558).

In stratified groups for NFG, IFG, EFG including stratification for sex we

found no significant correlation too.

Conclusion:

In a cross-sectional analysis of geriatic inpatients we

revealed no correlation between fasting blood glucose levels including

stratification for NFG, IFG, and EFG and cognitive testing using the

MMSE.

P-647

Comparison of mini nutritional assessment short and long form

and serum albumin as predictors of short- and long-term hip

fracture outcomes

H. Helminen

1

, T. Luukkaala

2

, J. Saarnio

3

, M. Nuotio

1

.

1

Seinäjoki Central

Hospital, Seinäjoki,

2

Science Center of Pirkanmaa Hospital District,

Tampere,

3

Oulu University Hospital, Oulu, Finland

Introduction:

Malnutrition is common among older hip fracture

patients and associated with adverse outcomes. The aim here was

to examine Mini Nutritional Assessment short (MNA-SF) and long

form (MNA-LF) and serum albumin as predictors of mobility, living

arrangements and mortality after hip fracture.

Methods:

Population-based prospective data were collected on 536

hip fracture patients aged 65 year and over. MNA-SF, MNA-LF and

serum albumin were assessed on admission. The outcomes were

declined mobility level, moving into a more assisted living accommo-

dation and mortality one month, four months and one year after the

fracture. Logistic regression analyses for mobility and living arrange-

ments with odds ratios (OR) and Cox proportional hazards model for

mortality with hazard ratios (HR) and 95%conficence intervals (CI)

were used, adjusted for age, gender, ASA grade and fracture type.

Results:

All measures predicted mortality at all time-points. Both risk

of malnutrition and malnutrition as measured by the MNA-LF

predicted mobility and living arrangements within four months of

the hip fracture. At one year, risk of malnutrition predicted mobility

and malnutrition predicted living arrangements, when measured by

the MNA-LF. Malnutrition, but not risk of malnutrition, as measured by

the MNA-SF predicted significantly living arrangements at all time-

points. One-month mobility was not predicted by any of the measures.

Poster presentations / European Geriatric Medicine 7S1 (2016) S29

S259

S199