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Table 1 Sociodemographic and Clinical Characteristics (n = 220)

From: Cholinesterase inhibitors do not alter the length of stay in nursing homes among patients with Alzheimer’s disease: a prospective, observational study of factors affecting survival time from admission to death

 

At the start of ChEI treatment

At nursing-home placementa

Variable

n/%

n/%

Female sex

161/73 %

na

APOE genotype, (n = 208)

 

na

 No ε4 alleles

57/27 %

 

 One ε4 allele

118/57 %

 

 Two ε4 alleles

33/16 %

 

Solitary living

116/53 %

126/57 %

Antihypertensive/cardiac therapy

79/36 %

 

Antidiabetics

9/4 %

 

Asthma medication

9/4 %

 

Thyroid therapy

19/9 %

 

Lipid-lowering agents

15/7 %

 

Estrogens

17/8 %

 

NSAIDs/acetylsalicylic acid

63/29 %

 

Antidepressants

71/32 %

 

Antipsychotics

14/6 %

 

Anxiolytics/sedatives/hypnotics

41/19 %

 

Variable

Mean ± standard deviation

Estimated age at onset of AD, years

73.5 ± 6.9

na

Estimated duration of AD, years

3.4 ± 2.6

5.1 ± 2.7

Age, years

76.9 ± 5.9

78.6 ± 5.8

Education, years

9.2 ± 2.3

na

MMSE score

20.1 ± 4.0

17.5 ± 5.7

ADAS-cog score (0–70)

24.0 ± 9.7

29.2 ± 12.5

IADL score

18.3 ± 5.1

22.7 ± 4.7

PSMS score

8.2 ± 2.8

10.5 ± 3.9

Number of concomitant medicationsa

3.0 ± 2.4

 

Home-help service, h/week

6.6 ± 5.4

(n = 56)

5.7 ± 6.5

(n = 180)

Adult day care, days/week

3.2 ± 1.7

(n = 23)

3.0 ± 1.4

(n = 82)

Mean dose of ChEI during the SATS, mg

  

 Donepezil (n = 138)

6.8 ± 1.8

na

 Rivastigmine (n = 37)

5.7 ± 1.9

na

 Galantamine (n = 45)

15.1 ± 3.2

na

Time to nursing home placement from the start of ChEI therapy, months

19.5 ± 10.0

na

Age at death, years

82.6 ± 6.0

na

  1. AD Alzheimer’s disease, ADAS-cog Alzheimer’s Disease Assessment Scale – cognitive subscale, APOE apolipoprotein E, ChEI cholinesterase inhibitor, IADL Instrumental Activities of Daily Living scale, MMSE Mini-Mental State Examination, na not applicable, NSAIDs nonsteroidal anti-inflammatory drugs, PSMS Physical Self-Maintenance Scale, SATS Swedish Alzheimer Treatment Study
  2. aConcomitant medications were not recorded at the postbaseline visits