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Table 4 Contribution of MOH-3 towards OI in the presence of potential confounders

From: Insights into the clinical management of the syndrome of supine hypertension – orthostatic hypotension (SH-OH): The Irish Longitudinal Study on Ageing (TILDA)

Full sample

B

Std. error

P

Odds ratio

95% wald confidence interval for odds ratio

Lower

Upper

MOH-3

0.39

0.08

<0.001

1.47

1.25

1.73

Female sex

−0.17

0.06

0.008

0.84

0.74

0.96

N05C (hypnotics, sedatives)

0.60

0.17

<0.001

1.83

1.31

2.54

Heart attack

0.47

0.16

0.004

1.59

1.16

2.19

3 or more chronic diseases

0.18

0.08

0.023

1.19

1.02

1.39

Any IADL disability

0.32

0.16

0.048

1.38

1.00

1.90

Age

−0.02

0.00

<0.001

0.98

0.98

0.99

MMSE

−0.04

0.02

0.043

0.96

0.93

1.00

Subsample ≥70 years old

B

Std. error

P

Odds ratio

95% wald confidence interval for odds ratio

Lower

Upper

C08C (peripheral CCB)

−0.53

0.22

0.015

0.59

0.39

0.90

N03A (antiepileptics)

0.91

0.44

0.036

2.50

1.06

5.86

3 or more chronic diseases

0.38

0.15

0.011

1.46

1.09

1.95

  1. Dependent variable: phasic OI. Binary logistic response, forward conditional procedure. Predictors entered: female sex, polypharmacy, C01A (cardiac glycosides), C01B (antiarrhythmics), C07A (beta blockers), C03 (diuretics), C09A (ACE-i), C09C (ARA), C08C (peripheral CCB), C08D (cardiac CCB), C02C (alpha blockers), C01D (cardiac vasodilators), C04A (peripheral vasodilators), N03A (antiepileptics), N05A (antipsychotics), N05B (anxiolytics), N05C (hypnotics, sedatives), N06A (antidepressants), hypertension, angina, heart attack, heart failure, diabetes, stroke¸ TIA, abnormal heart rhythm, Parkinson’s disease, three or more chronic diseases, any IADL disability, age, MOH-3, MMSE.