Regular Research Article
Development of a Short Form of the Severe Impairment Battery

https://doi.org/10.1097/00019442-200511000-00011Get rights and content

Objective

The authors sought to develop a short form of the Severe Impairment Battery (SIB).

Methods

Authors describe the development of an empirically-derived short form of the SIB (SIB–S) by use of data from 191 subjects with severe dementia in the United States and France.

Results

Mean (standard deviation) Mini-Mental State Exam scores for the American and French samples were 7.7 (4.8) and 5.7 (3.4), respectively, and original SIB scores were 71.87 (18.34) and 58.38 (26.86), respectively. Exploratory factor analyses were conducted separately and in combination for the two samples, to determine the number of clinically meaningful factors. An eight-factor model, explaining 60.2% of the common variance, was selected. The eight constructs were described as: expressive language, memory (verbal and nonverbal), social interaction, color-naming, praxis, reading and writing, fluency, and attention. Derived SIB–S scores were 38.41 (9.12) and 29.79 (13.17) for the American and French samples, respectively.

Conclusions

The original SIB is a valid and reliable research tool developed to enable reliable assessment of patients with severe dementia; it takes approximately 30 minutes to administer. The SIB–S takes only 10–15 minutes to administer, making it more appropriate for use in patients with very severe dementia, while it maintains the attributes of the original SIB.

Section snippets

Subjects

SIB data were available from two samples (total N = 191). Sample 1 consisted of 87 individuals living in Pittsburgh, PA (United States). Twenty-six individuals were participants in the clinical study “Serotonergic Pharmacotherapy for the treatment of Agitation in patients with Dementia” (SPAD), which has been previously described.21 The remaining 61 individuals in Sample 1 were subjects from the Alzheimer's Disease Research Center (ADRC) at the University of Pittsburgh Medical Center. A

RESULTS

The mean age (standard deviation [SD]) of the American sample was 77.1 (10.5) years, and the mean age of the French sample was 87.2 (7.8) years. The majority of subjects were women (American sample: 60.8%; French sample: 86.5%). The mean MMSE scores for the American sample and the French sample were 7.7 (4.8) and 5.7 (3.4), respectively, and for the SIB scores were 71.87 (18.34) and 58.38 (26.86), respectively. The two groups were significantly different in age (t[189] = 7.4; p <0.001),

DISCUSSION

There are very few scales that are appropriate for the assessment of cognitive functioning in patients with severe dementia. The significant cognitive and behavioral dysfunction typically seen in patients with scores in the lower half of the MMSE range (i.e., <15) presents a challenge to the accurate and reliable measurement of cognitive abilities. There are three scales that have been shown to be particularly useful with this population: the SIB, The Severe Cognitive Impairment Profile (SCIP),

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      Citation Excerpt :

      The short form of the SIB (SIB-S) may rectify these issues. The SIB-S can be administered in 10–15 minutes, and scores are significantly and highly correlated to the original SIB scores (rho = 0.99).37 Future studies may also consider assessing psychosocial functioning through validated assessments such as the Alzheimer's Disease Cooperative Study Activities of Daily Living Inventory for Severe Alzheimer's Disease (ADCS-ADL-Severe), as cognitive and functional impairment have been shown to correlate with one another in the advanced stages of AD.38

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    The French sample was recruited with the help of Marie-Pierre Hervy, M.D., at Kremlin Bicêtre Hospital; Anne-Sophie Rigaud, M.D., Ph.D., at Broca Hospital; Laurent Teillier, M.D., at Sainte Perine Hospital; François Piette, M.D., at Charles Foix Hospital, as well as Michel Roudier, M.D., Ph.D., and Jamal al-Aloucy, at Charles-Richet Hospital.

    The research reported in this article was supported in the United States by grants from the National Institute on Aging (AG05133) and the National Institute of Mental Health (MH59666, MH65416, and RR-00056) and in France by INSERM and by the Lundbeck Laboratory, with partial support from Eisai Laboratory.

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