Reliability, validity and clinical correlates of the Quality of Life in Alzheimer’s disease (QoL-AD) scale in medical inpatients
© The Author(s). 2016
Received: 27 November 2015
Accepted: 7 June 2016
Published: 14 June 2016
There is a lack of standardisation in quality of life (QoL) measurements to be used in older multimorbid patients. An ideal QoL measurement should be reliable, valid, subjective, multidimensional, feasible and generic. We hypothesised that the QoL-AD (Quality of Life in Alzheimer’s Disease) scale could have these properties. Our aim was to determine the psychometric properties and clinical correlations of QoL-AD in a population of elderly, multimorbid medical inpatients.
QoL-AD was performed in 200 medical inpatients, and available caregivers. Reliability was determined using cronbach’s alpha and corrected item-total correlations. The agreement between patient and proxy ratings were examined using intra-class correlations (ICC). Correlations between QoL-AD and demographic data, comorbidity, cognitive tests, ADL (activities of daily living) and depression were examined. To characterise the underlying constructs of QoL-AD, an exploratory factor analysis was performed.
In total, 199 patients fulfilled the QoL-AD rating, with 139 proxy ratings. Cronbach’s alpha (95 % CI) was 0.74 (0.68–0.79) for patients and 0.86 (0.83–0.90) for proxies. Patient-proxy ICC (95 % CI) was 0.31 (0.16–0.46). Lower QoL was correlated to depression, cognitive impairment, ADL impairment and solitary living, but not with comorbidity. The factor analysis gave a three-factor solution, with factors representing phsyical, social and psychological well-being.
The QoL-AD scale showed some promising properties but more research is needed before it can be recommended in this setting. If replicated, the finding that cognitive impairment, depression and ADL impairment were more associated with lower QoL than somatic comorbidity could have clinical implications for further studies aiming to improve QoL in this population.
KeywordsQuality of life Medical inpatients Scale validity
Quality of life (QoL) has been described by the World Health Organisation as “a broad ranging concept affected in a complex way by the person’s physical health, psychological state, level of independence, social relationships, personal beliefs and their relationship to salient features of their environment ”.
Multimorbidity, defined as having two or more chronic conditions is strongly associated with lower QoL [2–4]. A recent study showed that more than 60 % of primary care patients aged over 65 years were multimorbid . The association between QoL and multimorbidity is well established in community settings [2–4, 6–8]. Studies in hospital settings are much more scarce but suggest that multimorbidity could pose an even larger impact on QoL [9, 10].
Lack of standardisation in QoL measures in older age is a concern . An ideal QoL instrument in elderly should have been developed in an older population and include subjectivity and multidimensionality. It should be generic rather than disease-specific and at the same time brief and feasible .
Previous studies of QoL-AD
QoL-AD mean score
Item-total corr. (range)
Condé - Sala 
outpatients with AD
Living alone, sex, depression, ADL, NPI
mild to moderate AD
Depression, cognition, ADL
Depression, EQ-5Da, D-QoLb
mild to moderate AD
Cognition, mood, age, NPI
mild to moderate AD
Depression, NPI, cognition, ADL, WHOQoLa
MCI or mild-moderate dementia
ADL, depression, cognition, NPI, comorbidity
Depression, ADL, NPI, Eq-VASa, Qualidb
mild to moderate AD
Duke health profilea, NPI
probable or possible AD
Torisson (this study)
ADL, depression, living alone, cognition
In a previous study, we found that undetected cognitive impairment was frequent in medical inpatients . We hypothesised that the QoL-AD could be a suitable measurement in this setting. In the present study, we aim to determine the clinical correlations, reliability and validity of QoL-AD in this elderly, multimorbid hospital population.
The current study constitutes a secondary analysis, patients were concurrently participating in a previously published prospective intervention study .
The study was carried out at the department of General Internal Medicine at Skåne University Hospital in Malmö, the third largest city in Sweden, with approximately 300.000 citizens. The hospital is the only inpatient facility in the city, providing tertiary care to its inhabitants. Patients at the wards of the department of General Internal Medicine are primarily elderly with multiple conditions. The majority of patients are admitted through the hospital’s emergency department, with a wide variety of presenting complaints. Many patients receive community care at home and undergo discharge planning before returning home or to an institutional living.
Admitted patients over 60 years of age and living in a non-institutional living were considered eligible. Exclusion criteria included hospital-associated criteria (transfer to another department/intensive care, discharge before inclusion, isolation due to contagious disease). Patients had to be able to perform cognitive and functional tests, therefore patients with language barrier, terminal disease, blindness, deafness, aphasia or altered conciousness were excluded as well. In all, two hundred patients were included, the study inclusion has been described in detail before, including a detailed flowchart .
Included patients were taking part in a concurrent intervention study aiming to increase quality of care. Interventions included a comprehensive medication overview, liaison with GP at discharge, improved discharge planning and post-discharge telephone follow-up. Of the 200 patients, 99 patients received the interventions and 101 patients standard care. Group allocation (control/intervention) was carried out using convenience sampling through geographic selection, i.e. the study was not randomised.
The patients underwent a baseline measurement consisting of an interview (with a caregiver if available), medical record review, cognitive tests, functional tests and the QoL measurment.
To measure comorbidity, the Charlson comorbidity index was used . As an alternative measure, the total number of drugs was noted (drugs taken “as needed” were not included). This data were retreived from interviews first and then completed with data from electronic medical records.
Cognitive impairment was measured with the mini-mental state examination (MMSE) and the clock-drawing test (CDT) [28, 29]. Both tests were carried out during the hospitalisation, in a calm environment at the ward, when the patients were stabilised. MMSE ranges from from 0 (worst) to 30 (best). The CDT was rated using the six-point scale of Shulmann, ranging from 0 (worst) to 5 (best) .
The Gottfries-Bråne-Steen, or GBS, scale was also employed [30, 31]. This scale is comprised of four subsets: intellectual functions, emotional functions, ADL functions (activities of daily living) and symptoms. For the current study, the GBS-ADL subset and the “depressed mood” symptom was considered. The GBS-ADL subset is performance-based and comprised of six items (dressing, food intake, physical activity, spontaneous activity, continence and toileting). These are rated from 0 (best) to 6 (worst), for a total score of 0–36. As a proxy for ADL impairment we included the anamnestic data regarding access to community home care (yes/no). The GBS “depressed mood” symptom was also rated from 0 (best) to 6 (worst). As an alternative estimate of depression, we noted if patients were taking antidepressants (yes/no). Any drug in group N06A in the ATC (Anathomical Therapeutic Chemical) classification system was considered an antidepressant. Thus, two measures were collected each regarding physical comorbidity, cognitive impairment, ADL impairment and depression.
Quality of Life in Alzheimer’s disease scale (QoL-AD)
The QoL-AD scale was developed by Logsdon et al. [12, 19]. The QoL-AD is comprised of 13 items (physical health, energy, mood, living situation, memory, family, marriage, friends, self as a whole, ability to do chores, ability to do things for fun, money and life as a whole). Response options include 1(poor), 2(fair), 3(good) and 4 (excellent), for a total score of 13–52, with higher scores indicating better QoL.
The patients’ ratings were performed in an interview, with standardised instructions to avoid influencing the results. Interviews were done in a calm environment at the hospital ward by a team of two occupational therapists and a nurse, all of whom had received special training prior to the study. Caregiver ratings were done separately, using a questionnaire.
The patient and caregiver ratings were combined into a weighted composite score in the same way as in the original paper by Logsdon et al.: (2 × patient score + 1 × caregiver score)/3 .
Several studies have used factor analysis to describe underlying constructs in the QoL-AD, with diverse results [13–16, 22]. The most comprehensive of these studies, that perform exploratory and confirmatory factor analysis in a large sample of non-demented elderly, has reached a three-factor solution, with factors representing physical, social and psychological domains of quality of life .
For QoL-AD, we used the strategy suggested in the original paper on missing values . If a case had one or two missing items, they were imputed with that case’s mean value. If more than two items were missing, the case was discarded.
Internal consistency of QoL-AD was determined using Cronbach’s alpha, where a value of >0.7 is generally considered desirable. In addition, corrected item-total correlations between the 13 separate items and the total score were determined. Ideally, these should reach > 0.3 for all items. The conformity of patient and caregiver ratings was determined using a two-way mixed model single-measure intra-class correlation coefficient (ICC). The mean difference between the total score of patient and caregiver ratings was tested using a paired-sample t test.
Clinical associations were determined by using the Spearman’s correlations with the other baseline measurements, for each of the 13 QoL-AD items separately and with the Pearson correlation for the total score. A crude Bonferroni correction for multiple comparisons was utilised (all p values were multiplied with the number of variables, 12. Thus a p value of 0.004 was needed for a correlation to be considered significant). Control/intervention allocation in the concurrent intervention study was included as well, to detect selection bias.
Construct validity was also examined using an exploratory factor analysis on the QoL-AD items. Factorability was determined using Bartlett’s test of sphericity and the Kaiser-Mayer-Olkin test, where the latter should ideally exceed 0.5. Extraction was done on the correlation matrix, using principal factor analysis. Factors with Eigenvalues > 1 were retained. Factors were rotated using an orthogonal Varimax rotation [32, 33].
All analyses were carried out using SPSS version 20.0.
Of the 200 patients, 199 finished the QoL-AD rating. A total of four datapoints were missing (one each on “marriage”, “living situation”, “ability to do chores” and “life as a whole”) and were imputed accordingly. The caregivers completed 141 ratings. Of these, two ratings were missing more than two items and were discarded. In the remaining 139, eight datapoints were missing (two “family” and six “marriage”) and were imputed. No other imputations were done.
Full sample n = 199
Subset with caregiver rating n = 139
130 (65 %)
94 (68 %)
134 (67 %)
90 (65 %)
Comorbidity - Charlson comorbidity index
Comorbidity - Number of drugs
Cognition - Mini-mental state examination
Cognition - Clock-drawing test
Function - GBS - ADL
Function - Home care
118 (59 %)
79 (57 %)
Depression - GBS - depression
Depression - On antidepressants
31 (16 %)
21 (15 %)
Intervention in original study
99 (50 %)
60 (43 %)
Patient and caregiver scores on QoL-AD
Patient score mean (SD)
Caregiver score mean (SD)
Composite score mean (SD)
ICC patient - caregiver
Self as a whole
Ability to do chores
Ability to do things for fun
Life as a whole
Item-total correlations patient
Item-total correlations caregiver
Item-total correlations composite
Self as a whole
Ability to do chores
Ability to do things for fun
Life as a whole
No. of drugs
GBS - mood
Group in original study
Factor 1: physical
Factor 2: social
Factor 3: psychological
Ability to do things for fun
Ability to do chores
Life as a whole
Self as a whole
In this study, we employed the QoL-AD for the first time in a medical hospital population. Analysis of reliability and validity were largely similar to previous studies, suggesting that QoL-AD may be suitable for this population. Regarding clinical associations, we found that lower QoL was associated with depression, cognitive impairment, ADL impairment and solitary living.
In a recent comprehensive study, using data from two clinical trials of Bapinezeumab in patients with mild to moderate Alzheimer’s disease, Lacey and colleagues evaluated the utility of the QoL-AD scale . The authors found that patient-rated QoL-AD was lower than caregiver-rated, consistent with all previous QoL_AD studies. Furthermore, the authors found that QoL-AD was only weakly associated with clinical measures of cognition and function, with caregiver-rated QoL-AD having a slightly stronger association with clinical measures. The authors concluded that QoL-AD was not suited to measure disease progression.
Albeit in a different setting, this pattern is partly reoccuring in our study, patients rated their QoL higher than their caregivers. The intra-class correlation between patient and proxy ratings were modest with an ICC of 0.31, in line with previous studies [19, 22, 35]. Also, regarding clinical associations, there was a discrepancy with caregiver ratings having stronger correlations with clinical measures than patients’ ratings. Specifically, this concerned cognitive tests, with no correlation for the self-reported score, a finding shown in several other studies [35–37].
Lacey et al. suggest that this pattern could be attributed to lacking insight as a consequence of cognitive impairment . However, other studies have not been able to prove an effect of lacking insight on QoL ratings in milder forms of dementia [35, 37]. Our population was not demented but rather multimorbid. Another possible explanation is adaptation, or what is known as “response shift”, a gradual adjustment to chronic disease that has been shown in other diseases as well . According to this hypothesis, patients adapt to a lower level of function, while caregivers retain a former, higher, level as their benchmark .
Concerning physical comorbidity, neither the highly established Charlson index nor number of drugs were associated with QoL-AD score. This is an interesting finding, as our study is the first using QoL-AD in a somatic hospital setting. One possible explanation is that the QoL-AD does not measure the effect of physical health on QoL in the expected way and thus is not a valid QoL measurement for this population. Another possibility is that these patients, and their caregivers, actually consider mental health and cognitive impairment to have a much larger impact on QoL than physical comorbidity.
In the factor analysis, we found a three-factor solution, containing the factors “physical well-being”, “social well-being” and “psychological well-being”. This structure with three different constructs is the exact same that was found in non-demented community-dwelling elderly in a high-quality previous study . According to the WHO definition, QoL is a multi-dimensional concept and the three-factor solution with physical, mental and social domains is similar to many other theoretical constructs, including for example the Neuro-QoL initiative .
An ideal QoL instrument in this setting should be subjective, multidimensional, generic and feasible. The only prerequisite not fulfilled by QoL-AD is that it was not developed as a generic measure but a disease-specific measure for Alzheimer’s disease. However, only one of 13 items directly concerns cognitive impairment (the memory item). Interestingly, a new scale, the WHOQOL-AGE, has been developed as a generic instrument for use in the elderly . The WHOQOL-AGE is very similar to the QoL-AD, it contains 13 items rated from 1 to 5, of which 9 have direct counterparts in the QoL-AD. This similarity between these two scales supports the impression that QoL-AD may have more generic properties than originally thought.
However, the WHOQOL-AGE does not include cognitive impairment. Whether cognitive impairment should be seen as a core aspect of QoL or a predictor of QoL could be debated. In our material, 73 % had cognitive impairment, of which the majority were undetected previously. Furthermore, the memory item by itself had a correlation with MMSE of 0.45 for the composite score, see Additional file 1: Table S1. Thus, in our opinion, cognitive impairment should be a part of the QoL assessment in this setting.
Looking ahead, there are several other state-of-the-art initiatives , such as PROMIS (patient reported outcomes measurement information system) (www.nihpromis.org) and NeuroQoL that could possibly adress the multimorbidity issue . These systems apply item response theory (IRT) and computer adaptive testing (CAT) to tailor a test, where the reply on one item is used to select the next one from a large item bank. This results in an individual score that is comparable across a range of conditions. The concept of adaptive individual testing in multimorbid elderly patients is very appealing, as it could combine generic and disease-specific properties. At the same time, with the right algorithm, the test could be broad-ranging, brief and precise.
Until such instruments are implemented generally, the lack of standardisation is a concern. In a review including 37 studies on QoL in older patients, a total of 28 different QoL measures were used, most of them developed for younger populations . Only 3 generic QoL scales addressed cognitive impairment, the briefest one including 68 items.
The QoL-AD showed some promising properties but it is to early to recommend QoL-AD in this setting without further research. A prospective study could determine the feasibility and validity of QoL-AD and compare it to other relevant QoL measures. A larger study could perform multivariate analysis to further analyse clinical correlates, controlling for the other parameters and address multicolinearity.
In the present study, cognitive impairment, ADL impairment and depression were more strongly associated with lower QoL than physical comorbidity. This could have important clinical implications. Today, physical health and social aspects are routinely adressed in medical inpatients. The same does not apply to cognitive impairment and depression which are often undetected, despite being associated with adverse outcomes [25, 40, 41]. If our findings were to be replicated, it would be yet another reason to increase acknowledgement of these issues in order to improve quality of life.
ADL, activities of daily living; CDT, clock-drawing test; CI, confidence interval; GBS, Gottfries-Bråne-Steen scale; ICC, intra-class correlation; MMSE, mini-mental state examination; QoL, quality of life; QoL-AD, Quality of Life in Alzheimer’s disease
We would like to thank Anna Johansson, Jenny Cappelin and Sofia Raccuia for assistance with acquisition of data.
This study was financed by the Swedish Research Council (Vetenskapsrådet #523-2010-520), the Swedish Brain Power programme, the National Swedish Board of Health and Welfare and the Governmental Funding of Clinical Research within the National Health Services (ALF). All researchers acted independently to the funding bodies. The funding agencies had no role in study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the article for publication.
Availability of data and materials
Data sharing consent was not obtained. Lawyers at the Swedish Data Inspection Board, the Data Protection Officer at Skåne University Hospital and the Research Ethics Advisor at Lund University have unanimously advised us that public sharing of our data would not be compatible with Swedish legislation. Requests for data access may be sent to firstname.lastname@example.org or Elisabet.Londos@skane.se. Such requests will be evaluated individually by the Data Protection Officer at Lund University according to the Swedish Personal Data Act.
LM and LS conceived the study. Data analysis, statistics and figure preparation were done by GT. The manuscript was drafted by GT and EL. LM and LS critically reviewed the manuscript. The final version was approved by all authors. GT is the guarantor.
All authors have completed the ICMJE uniform disclosure form at www.icmje.org/coi_disclosure.pdf and declare: no financial relationships with any organisations that might have an interest in the submitted work in the previous three years; no other relationships or activities that could appear to have influenced the submitted work.
All patients enrolled in the original study gave written informed consent. Both the original study and the secondary analysis have been approved by the regional ethics committee at Lund University.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- The WHOQOL Group. The World Health Organization Quality of Life assessment (WHOQOL): position paper from the World Health Organization. Soc Sci Med. 1995; 41:1403–1409.Google Scholar
- Brettschneider C, Leicht H, Bickel H, Dahlhaus A, Fuchs A, Gensichen J, Maier W, Riedel-Heller S, Schafer I, Schon G, et al. Relative impact of multimorbid chronic conditions on health-related quality of life--results from the MultiCare Cohort Study. PLoS One. 2013;8:e66742.View ArticlePubMedPubMed CentralGoogle Scholar
- Heyworth IT, Hazell ML, Linehan MF, Frank TL. How do common chronic conditions affect health-related quality of life? Br J Gen Pract. 2009;59:e353–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Hunger M, Thorand B, Schunk M, Doring A, Menn P, Peters A, Holle R. Multimorbidity and health-related quality of life in the older population: results from the German KORA-age study. Health Qual Life Outcomes. 2011;9:53.View ArticlePubMedPubMed CentralGoogle Scholar
- Barnett K, Mercer SW, Norbury M, Watt G, Wyke S, Guthrie B. Epidemiology of multimorbidity and implications for health care, research, and medical education: a cross-sectional study. Lancet. 2012;380:37–43.View ArticlePubMedGoogle Scholar
- Marengoni A, Angleman S, Melis R, Mangialasche F, Karp A, Garmen A, Meinow B, Fratiglioni L. Aging with multimorbidity: a systematic review of the literature. Ageing Res Rev. 2011;10:430–9.View ArticlePubMedGoogle Scholar
- Garin N, Olaya B, Moneta MV, Miret M, Lobo A, Ayuso-Mateos JL, Haro JM. Impact of multimorbidity on disability and quality of life in the spanish older population. PLoS One. 2014;9:e111498.View ArticlePubMedPubMed CentralGoogle Scholar
- Mujica-Mota RE, Roberts M, Abel G, Elliott M, Lyratzopoulos G, Roland M, Campbell J. Common patterns of morbidity and multi-morbidity and their impact on health-related quality of life: evidence from a national survey. Qual Life Res. 2015;24(4):909-18.Google Scholar
- Helvik AS, Engedal K, Krokstad S, Selbaek G. A comparison of life satisfaction in elderly medical inpatients and the elderly in a population-based study: Nord-Trondelag Health Study 3. Scand J Public Health. 2011;39:337–44.View ArticlePubMedGoogle Scholar
- Helvik AS, Engedal K, Selbaek G. The quality of life and factors associated with it in the medically hospitalised elderly. Aging Ment Health. 2010;14:861–9.View ArticlePubMedGoogle Scholar
- Hickey A, Barker M, McGee H, O’Boyle C. Measuring health-related quality of life in older patient populations: a review of current approaches. Pharmacoeconomics. 2005;23:971–93.View ArticlePubMedGoogle Scholar
- Logsdon R, Gibbons LE, McCurry SM, Teri L. Quality of Life in Alzheimer’s Disease: patient and caregiver reports. J Ment Health Aging. 1999;5:21–32.Google Scholar
- Buasi N, Permsuwan U. Validation of the Thai QOL-AD version in Alzheimer’s patients and caregivers. Australas Med J. 2014;7:251–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Larsson V, Engedal K, Aarsland D, Wattmo C, Minthon L, Londos E. Quality of life and the effect of memantine in dementia with lewy bodies and Parkinson’s disease dementia. Dement Geriatr Cogn Disord. 2011;32:227–34.View ArticlePubMedGoogle Scholar
- Revell AJ, Caskie GI, Willis SL, Schaie KW. Factor structure and invariance of the Quality of Life in Alzheimer’s Disease (QoL-AD) Scale. Exp Aging Res. 2009;35:250–67.View ArticlePubMedPubMed CentralGoogle Scholar
- Thorgrimsen L, Selwood A, Spector A, Royan L, de Madariaga Lopez M, Woods RT, Orrell M. Whose quality of life is it anyway? The validity and reliability of the Quality of Life-Alzheimer’s Disease (QoL-AD) scale. Alzheimer Dis Assoc Disord. 2003;17:201–8.View ArticlePubMedGoogle Scholar
- Barrios H, Verdelho A, Narciso S, Goncalves-Pereira M, Logsdon R, de Mendonca A. Quality of life in patients with cognitive impairment: validation of the Quality of Life-Alzheimer’s Disease scale in Portugal. Int Psychogeriatr. 2013;25:1085–96.View ArticlePubMedGoogle Scholar
- Leon-Salas B, Logsdon RG, Olazaran J, Martinez-Martin P, The M-A. Psychometric properties of the Spanish QoL-AD with institutionalized dementia patients and their family caregivers in Spain. Aging Ment Health. 2011;15:775–83.View ArticlePubMedGoogle Scholar
- Logsdon RG, Gibbons LE, McCurry SM, Teri L. Assessing quality of life in older adults with cognitive impairment. Psychosom Med. 2002;64:510–9.View ArticlePubMedGoogle Scholar
- Matsui T, Nakaaki S, Murata Y, Sato J, Shinagawa Y, Tatsumi H, Furukawa TA. Determinants of the quality of life in Alzheimer’s disease patients as assessed by the Japanese version of the Quality of Life-Alzheimer’s disease scale. Dement Geriatr Cogn Disord. 2006;21:182–91.View ArticlePubMedGoogle Scholar
- Novelli MM, Nitrini R, Caramelli P. Validation of the Brazilian version of the quality of life scale for patients with Alzheimer’s disease and their caregivers (QOL-AD). Aging Ment Health. 2010;14:624–31.View ArticlePubMedGoogle Scholar
- Wolak A, Novella JL, Drame M, Guillemin F, Di Pollina L, Ankri J, Aquino JP, Morrone I, Blanchard F, Jolly D. Transcultural adaptation and psychometric validation of a French-language version of the QoL-AD. Aging Ment Health. 2009;13:593–600.View ArticlePubMedGoogle Scholar
- Conde-Sala JL, Garre-Olmo J, Turro-Garriga O, Lopez-Pousa S, Vilalta-Franch J. Factors related to perceived quality of life in patients with Alzheimer’s disease: the patient’s perception compared with that of caregivers. Int J Geriatr Psychiatry. 2009;24:585–94.View ArticlePubMedGoogle Scholar
- Bosboom PR, Alfonso H, Eaton J, Almeida OP. Quality of life in Alzheimer’s disease: different factors associated with complementary ratings by patients and family carers. Int Psychogeriatr. 2012;24:708–21.View ArticlePubMedGoogle Scholar
- Torisson G, Minthon L, Stavenow L, Londos E. Cognitive impairment is undetected in medical inpatients: a study of mortality and recognition amongst healthcare professionals. BMC Geriatr. 2012;12:47.View ArticlePubMedPubMed CentralGoogle Scholar
- Torisson G, Minthon L, Stavenow L, Londos E. Multidisciplinary intervention reducing readmissions in medical inpatients: a prospective, non-randomized study. Clin Interv Aging. 2013;8:1295–304.View ArticlePubMedPubMed CentralGoogle Scholar
- Charlson M, Szatrowski TP, Peterson J, Gold J. Validation of a combined comorbidity index. J Clin Epidemiol. 1994;47:1245–51.View ArticlePubMedGoogle Scholar
- Folstein MF, Folstein SE, McHugh PR. “Mini-mental state”. A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975;12:189–98.View ArticlePubMedGoogle Scholar
- Shulman KI. Clock-drawing: is it the ideal cognitive screening test? Int J Geriatr Psychiatry. 2000;15:548–61.View ArticlePubMedGoogle Scholar
- Brane G, Gottfries CG, Winblad B. The Gottfries-Brane-Steen scale: validity, reliability and application in anti-dementia drug trials. Dement Geriatr Cogn Disord. 2001;12:1–14.View ArticlePubMedGoogle Scholar
- Gottfries CG, Brane G, Gullberg B, Steen G. A new rating scale for dementia syndromes. Arch Gerontol Geriatr. 1982;1:311–30.View ArticlePubMedGoogle Scholar
- Henson RK, Roberts JK. Use of exploratory factor analysis in published research - Common errors and some comment on improved practice. Educ Psychol Meas. 2006;66:393–416.View ArticleGoogle Scholar
- Thompson BD, Daniel LG. Factor analytic evidence for the construct validity of scores: a historical overview and some guidelines. Educ Psychol Meas. 1996;56:197–208.View ArticleGoogle Scholar
- Lacey L, Bobula J, Rudell K, Alvir J, Leibman C. Quality of life and utility measurement in a large clinical trial sample of patients with mild to moderate Alzheimer’s disease: determinants and level of changes observed. Value Health. 2015;18:638–45.View ArticlePubMedGoogle Scholar
- Banerjee S, Samsi K, Petrie CD, Alvir J, Treglia M, Schwam EM, del Valle M. What do we know about quality of life in dementia? A review of the emerging evidence on the predictive and explanatory value of disease specific measures of health related quality of life in people with dementia. Int J Geriatr Psychiatry. 2009;24:15–24.View ArticlePubMedGoogle Scholar
- Naglie G, Hogan DB, Krahn M, Beattie BL, Black SE, Macknight C, Freedman M, Patterson C, Borrie M, Bergman H, et al. Predictors of patient self-ratings of quality of life in Alzheimer disease: cross-sectional results from the Canadian Alzheimer’s Disease Quality of Life Study. Am J Geriatr Psychiatry. 2011;19:881–90.View ArticlePubMedPubMed CentralGoogle Scholar
- Woods RT, Nelis SM, Martyr A, Roberts J, Whitaker CJ, Markova I, Roth I, Morris R, Clare L. What contributes to a good quality of life in early dementia? Awareness and the QoL-AD: a cross-sectional study. Health Qual Life Outcomes. 2014;12:94.View ArticlePubMedPubMed CentralGoogle Scholar
- National Institute of Neurological Disorders and Stroke (NINDS). User manual for the Quality of Life in Neurological disorders (Neuro-QoL) measures. 2015. Version 2.0.Google Scholar
- Caballero FF, Miret M, Power M, Chatterji S, Tobiasz-Adamczyk B, Koskinen S, Leonardi M, Olaya B, Haro JM, Ayuso-Mateos JL. Validation of an instrument to evaluate quality of life in the aging population: WHOQOL-AGE. Health Qual Life Outcomes. 2013;11:177.View ArticlePubMedPubMed CentralGoogle Scholar
- Bowler C, Boyle A, Branford M, Cooper SA, Harper R, Lindesay J. Detection of psychiatric disorders in elderly medical inpatients. Age Ageing. 1994;23:307–11.View ArticlePubMedGoogle Scholar
- Mukadam N, Sampson EL. A systematic review of the prevalence, associations and outcomes of dementia in older general hospital inpatients. Int Psychogeriatr. 2011;23:344–55.View ArticlePubMedGoogle Scholar