J Clin Med Res
Journal of Clinical Medicine Research, ISSN 1918-3003 print, 1918-3011 online, Open Access
Article copyright, the authors; Journal compilation copyright, J Clin Med Res and Elmer Press Inc
Journal website http://www.jocmr.org

Original Article

Volume 7, Number 1, January 2015, pages 21-28


Validity and Reliability of the European Portuguese Version of Neuropsychiatric Inventory in an Institutionalized Sample

Ana Rita Ferreiraa, Sonia Martinsb, Orquidea Ribeiroc, Lia Fernandesd, e

aFaculty of Medicine, University of Porto, Al. Hernani Monteiro, 4200-319 Porto, Portugal
bResearch and Education Unit on Aging (UNIFAI), University of Porto, Rua Jorge de Viterbo Ferreira, no. 228, 4050-313 Porto, Portugal
cDepartment of Health Information and Decision Sciences (CIDES) and CINTESIS, Faculty of Medicine, University of Porto, Al. Hernani Monteiro, 4200-319 Porto, Portugal
dUNIFAI/CINTESIS Research Unit, Faculty of Medicine, University of Porto. Clinic of Psychiatry and Mental Health, CHSJ, Porto, Al. Hernani Monteiro, 4200-319 Porto, Portugal
eCorresponding Author: Lia Fernandes, Faculty of Medicine, University of Porto, Al. Hernani Monteiro, 4200-319 Porto, Portugal

Manuscript accepted for publication September 04, 2014
Short title: European Portuguese Version of NPI
doi: http://dx.doi.org/10.14740/jocmr1959w

Abstract▴Top 

Background: Neuropsychiatric symptoms are very common in dementia and have been associated with patient and caregiver distress, increased risk of institutionalization and higher costs of care. In this context, the neuropsychiatric inventory (NPI) is the most widely used comprehensive tool designed to measure neuropsychiatric Symptoms in geriatric patients with dementia. The aim of this study was to present the validity and reliability of the European Portuguese version of NPI.

Methods: A cross-sectional study was carried out with a convenience sample of institutionalized patients (≥ 50 years old) in three nursing homes in Portugal. All patients were also assessed with mini-mental state examination (MMSE) (cognition), geriatric depression scale (GDS) (depression) and adults and older adults functional assessment inventory (IAFAI) (functionality). NPI was administered to a formal caregiver, usually from the clinical staff. Inter-rater and test-retest reliability were assessed in a subsample of 25 randomly selected subjects.

Results: The sample included 166 elderly, with a mean age of 80.9 (standard deviation: 10.2) years. Three out of the NPI behavioral items had negative correlations with MMSE: delusions (rs = -0.177, P = 0.024), disinhibition (rs = -0.174, P = 0.026) and aberrant motor activity (rs = -0.182, P = 0.020). The NPI subsection of depression/dysphoria correlated positively with GDS total score (rs = 0.166, P = 0.038). NPI showed good internal consistency (overall α = 0.766; frequency α = 0.737; severity α = 0.734). The inter-rater reliability was excellent (intraclass correlation coefficient (ICC): 1.00, 95% confidence interval (CI) 1.00 - 1.00), as well as test-retest reliability (ICC: 0.91, 95% CI 0.80 - 0.96).

Conclusion: The results found for convergent validity, inter-rater and test-retest reliability, showed that this version appears to be a valid and reliable instrument for evaluation of neuropsychiatric symptoms in institutionalized elderly.

Keywords: Behavior disorders; Dementia; Aged; Neuropsychiatric inventory; Validation study

Introduction▴Top 

Since its first formal definition, Alzheimer’s disease (AD) has also included non-cognitive symptoms such as delusions, misidentification, hallucinations, anxiety, and apathy [1, 2]. However, behavioral and psychological symptoms were excluded from the main international classifications and diagnostic criteria, playing a secondary role within the diagnosis of dementia. Later, in 1996, those non-cognitive manifestations of dementia were defined by the International Psychogeriatric Association as “signs and symptoms of disturbed perception, thought, content, mood, or behavior that frequently occur in patients with dementia.” [3, 4] and a large number of population-based studies confirmed the presence of this heterogeneous group of symptoms and behaviors.

The near universal prevalence of behavioral and psychological symptoms of dementia (BPSD) in all dementia patients [5-8] at any disease stage and regardless of its etiology [9] has focused attention on reliable and valid measures of BPSD and effective and safe available treatments. According to Frisoni et al [10], 50% of patients with dementia have at least four BPSD simultaneously and its prevalence is likely to increase during the natural course of dementia [11] combined with seriously disabling effects on patients and caregivers.

The prevalence rates of BPSD largely depend on the type of the sample and the setting considered, being less frequent and severe in community-dwelling subjects with dementia than in hospitalized and institutionalized patients [12]. However, even in mildly impaired community-dwelling samples, the BPSD contribute significantly to the burden of dementia care [13]. Due to their high occurrence, BPSD have become a relevant and significant clinical and research targets [14-16].

BPSD have been referred as highly correlated with high levels of distress and caregiver burden, as well as with increased use of health care resources, risk of institutionalization [3, 17, 18] and mortality [19]. Additionally, approximately 50% of subjects with mild cognitive impairment (MCI) and 25% of those with normal cognition present at least one BPSD [20], suggesting that they can include early signs of dementia preceding the onset of cognitive deficits [21-23].

Taking this into consideration, the early recognition and accurate diagnosis of BPSD, based on valid and reliable assessment tools, appears as an important feature for its optimal treatment, contributing to decrease of associated adverse outcomes. BPSD assessment has been highly recognized as crucial to the management of dementia, and it has become an important aspect of dementia research worldwide [9].

In this context, the neuropsychiatric inventory (NPI) [24] is the most widely comprehensive tool used to assess behavioral and psychological disturbances, based on an informant interview format rating scale. The NPI has been translated and validated into a number of languages and is widely accepted as the standard measure of BPSD in clinical trials and in several population-based studies into dementia and related disorders [20, 25, 26]. This inventory has also been used as an outcome measure in various other research studies, for example to gather information that distinguishes among etiologies of dementia [24, 27], to measure longitudinal changes in BPSD in elderly nursing home residents [28] and to assess the effects of pharmacological treatments [29].

In the original studies [24, 30], the NPI showed good reliability and validity. Inter-rater reliability ranged from 93.6% to 100%, according to the subdomain considered, and test-retest reliability was also shown to be very high. Content validity was high, as rated by internationally recognized experts in geriatric psychiatry. As a whole, those results proved its robustness as a tool to assess BPSD across a variety of settings [26].

Although Portugal has one of the highest rates of mental disorders in Europe [31], little is known about BPSD prevalence and validated measures to achieve this goal are lacking.

The aim of this study was to contribute to the further understanding of the psychometric properties of the European Portuguese version of NPI, by presenting the preliminary results of its validation study in a geriatric nursing home sample.

Material and Methods▴Top 

Sample and procedures

A cross-sectional study was conducted with a convenience sample of institutionalized patients (≥ 50 years old) in three nursing homes in north of Portugal, between September 2012 and April 2013. All permanently institutionalized subjects were eligible for the study. However, subjects with delirium, those who were terminally ill, unable to speak Portuguese or who refused to participate were not included. The presence of BPSD was not considered to be a prerequisite to the inclusion in the study.

All subjects included were assessed with the following instruments: mini-mental state examination (MMSE) [32, 33], as a cognitive global measure, adults and older adults functional assessment inventory (IAFAI) [34], for functional assessment, and geriatric depression scale (GDS) [35, 36], as a measure of depressive symptomatology. The NPI was administered to a formal caregiver, usually from the clinical staff, for BPSD assessment. In order to fit the assessment protocol to the context of the investigation, previously validated versions of the instruments or versions adapted for the Portuguese population were used. In this study, the European Portuguese translation of NPI by Leitao and Nina [37] was used.

Complete demographic and clinical characteristics of the sample were obtained through chart review.

Regarding the inter-rater and test-retest reliability analysis, it was carried out in a sample of 25 randomly selected elderly people, recruited only from one of the nursing homes. In the inter-rater reliability process, two researchers completed the NPI independently and the interviewers were alternated. The test-retest reliability was determined by conducting a second NPI interview within 2 weeks.

All procedures concerning ethical approval were obtained from the board of the institutions where the study was held. All the necessary measures to safeguard participants’ anonymity and confidentiality of information were also thoroughly followed. Informed consent was obtained from the patient and/or from their legal representative.

Description of the instrument

NPI is an informant-based rating scale developed to assess neuropsychiatric symptoms in dementia. The instrument consists of 12 items, with each of them evaluating 12 common BPSD, including delusions, hallucinations, agitation/aggression, depression, anxiety, elation, apathy, disinhibition, irritability, aberrant motor behavior, and sleeping and eating disorders [24, 30]. The questions are approached in a comprehensive and time-efficient manner through the use of screening questions for each target behavior. If the behavior is absent, no further questions are needed; if present, more comprehensive information is obtained by a series of in-depth questions to probe specific symptomatology, its frequency (on a scale from 1 to 3) and severity (on a scale from 1 to 4).

The NPI total or composite score is calculated by multiplying the frequency and severity rates per domain (maximum score per domain is 12) and adding them up (minimum is 0 and maximum 144). Moreover, the same interview can register caregiver emotional distress for each item and for the whole scale [38].

Statistical analysis

Statistical analyses were performed using the Statistical Package for the Social Sciences Version 21.0 for Windows software (SPSS). Patient characteristics are presented as raw frequencies and percentages for categorical variables and as mean and standard deviation (SD) for continuous variables, when normality could be assumed and median, minimum, maximum or percentiles 5 and 95, otherwise. For comparing the distribution of the total NPI between two or more independent groups, Mann-Whitney or Kruskal-Wallis tests were used for continuous variables when normality could not be assumed. Convergent validity was explored by calculating Spearman’s p rank correlation coefficients between NPI domains and total scores for MMSE, GDS and IAFAI, at a significance level of 0.05. Cronbach’s coefficient alpha (α) was determined to assess internal consistency. Inter-rater and test-retest reliability were assessed by calculating the intraclass correlation coefficient (ICC) and 95% confidence intervals (CIs).

Results▴Top 

In the present study, a total of 166 participants was assessed. All participants lived in long-term care institutions. The main socio-demographic and clinical characteristics of the participants are presented in detail in Table 1.

Table 1. Demographic and Clinical Characteristics of Sample
 

The average NPI-total score for this sample was 6 (SD: 12), with a minimum of 0 and a maximum of 76. The most frequent neuropsychiatric domains were: sleep and nighttime behavior disorders (54%), delusions (22%), depression/dysphoria (19%), irritability/lability (17%) and agitation/aggression (15%) (Table 2). No significant correlations between NPI (domains and total) and age, gender and education level of the elderly were found.

Table 2. Frequency of NPI Domains
 

As expected a significant difference regarding total score of NPI (P = 0.007) was found, for higher values in the group with cognitive deficit, assessed by MMSE (mean rank 89.66 vs. 70.73).

Three out of the NPI behavioral items (frequency × severity) had significant negative correlations with MMSE: delusions (rs = -0.177, P = 0.024), disinhibition (rs = -0.174, P = 0.026) and aberrant motor activity (rs = -0.182, P = 0.020). The NPI domain of depression/dysphoria correlated positively with GDS total score (rs = 0.166, P = 0.038) (Table 3). A positive correlation between the total score of NPI and the cognitive domain of IAFAI (rs = 0.258; P = 0.002) was also found.

Table 3. Correlations Between NPI, MMSE and GDS
 

The NPI showed good internal consistency (overall α = 0.766; frequency α = 0.737; severity α = 0.734; distress α = 0.755). Cronbach’s alpha varied between 0.706 and 0.767 for product of frequency and severity; 0.673 - 0.738 for frequency, 0.676 - 0.735 for severity and 0.692 - 0.757 for distress in individual items (Table 4).

Table 4. Cronbach’s Alpha (α) for Individual Domains of NPI
 

To analyze the inter-rater and test-retest reliability, a subsample of 25 elderly, with a mean age of 81.6 (SD: 9.2), mostly female (76%), widowed (64%) and with lower educational level (92% ≤ 4 years) was used.

The inter-rater reliability was excellent for total (ICC: 1.00, 95% CI: 1.00 - 1.00) and for all domains of NPI (ICC: 1.00, 95% CI: 1.00 - 1.00).

The test-retest reliability was excellent for total (FxS ICC: 0.909, 95% CI: 0.80 - 0.96; distress ICC: 0.89, 95% CI: 0.766 - 0.950). The results for each NPI domains are presented in Table 5.

Table 5. Test-Retest Reliability
 
Discussion▴Top 

This study indicates that the European Portuguese version of NPI has good validity and reliability, presents significant convergent validity, as well as robust positive data on inter-rater and test-retest reliability.

In this study, the most frequent symptoms were the same found in previous studies [39-44], in particularly depression. Major depressive disorder, minor depression, dysthymia or subsyndromal, but still clinically significant depressive symptoms not only are common in the long term care facilities, but also appear to be common comorbid conditions with dementia. However, the most frequent behavioral symptom was related to sleep/nighttime domain. Several factors can contribute to sleep impairment. It is well known that age itself can induce alteration in sleep patterns [45] just like the medical conditions and medications. But sleep problems tend to be more common and severe in nursing home residents, which would be expected based on increase of age. Among the major factors, one can enumerate the nursing home environmental factors or the behavioral lifestyle associated with routines that conduct to inactivity during daylight hours [46]. Another explanation can be the possible association of poor quality of sleep with the prevalence of depression and depressive symptoms found in this sample.

Apathy also appears as one of the most frequent domains in these previous studies, but not in the present study. This can be explained in part by the fact that some of these studies included only patients with dementia [39, 40, 42] with the correlated potential for referral bias leading to higher frequency estimates in contrast with the present study that addressed both demented and healthy subjects which can explain the minor prevalence of this particular BPSD. On the other hand, clinicians often regard depression as a model for defining apathy, even if these concepts have to be distinguished.

The least common domains, namely euphoria, aberrant motor behavior, disinhibition and hallucinations, were similar to those found in previous studies [39, 42, 43]. In fact, neuropsychiatric symptoms are ubiquitous in nursing home demented patients, with prevalence rates above 80% [47] and the institutionalization must be taken into account as an important environmental factor.

Moreover, no significant correlations between the NPI (total and domains) with age, gender or education level of the elderly were found, which can be explained by the fact that neuropsychiatric symptoms might be independent of demographic variables. Some studies had already found this lack of correlation [40], but others found some correlation. For example, Mega et al [17] have demonstrated a significant association between male patients and agitation, and Cummings et al [24] have shown a significant relationship between apathy and age, with older patients being rated as more apathetic. Zuidema et al [48] also found that depression and anxiety were more frequent in female patients, and apathy in male institutionalized patients.

As in other studies [48], BPSD were associated with cognitive decline, with most symptoms occurring in those who showed decline.

The psychometric proprieties of the European Portuguese version of NPI seem to be in accordance with the original studies [24, 30], as well as with other previous international validation studies [39-44, 49-51].

This version also showed good convergent validity, corroborated by the correlations found with other measures. As in the original study [24], the same NPI domains (except for anxiety) were negatively correlated with MMSE. Moreover, a positive correlation between depression/dysphoria NPI domain and a depression assessment instrument (in the present study, the GDS) was also found in other previous studies [24, 49].

Regarding the inter-rater reliability, the values for total and for all domains of NPI, were higher than in other studies [43], with 100% of concordance between the two raters. This analysis demonstrates that this version is highly reliable when used by different examiners.

The previous validations studies also showed good test-retest correlations coefficients, ranging between 0.63 and 0.96 [24, 40, 50, 51]. In the present study, the test-retest reliability was assessed using ICC, presenting globally good values for total and for all domains, except for disinhibition and irritability/lability. These lowest values may reflect more variability in these behaviors or more difficulty for caregivers in reliably assessing and reporting these BPSD in response to NPI questions.

There is some heterogeneity in the methodological issues in the previous validation studies that need to be taken into consideration, such as the setting (outpatient vs. institutionalization), sample (patients only with dementia vs. patients without dementia) and statistical procedures. On the other hand, the differences in the results from the present study and those conducted in other countries may be related to different backgrounds, and differences in understanding and rating of the symptoms.

The strengths of this study were that, to our knowledge, this is the first validation study of the European Portuguese version of the NPI. Moreover, this validation process could also provide specific information regarding the neuropsychiatric symptoms of a sample of Portuguese elderly people. Finally, in the present study elderly with and without cognitive deficit were included, as well as patients with previous major psychiatric disorders (e.g. depression and schizophrenia), in some cases with a concurrent diagnosis of dementia.

This study presents some limitations. First, detailed information concerning some clinical characteristics (e.g. type of dementia) was not available. Second, pharmacological treatment was not controlled, so some substances could have induced, alleviated or eliminated some BPSD. Third, as this is a three-site study, validation of the performance of NPI will be required in other settings to assure generalizability. Further research should focus on the use of this instrument in various settings by different levels of health professionals.

In conclusion, the European Portuguese version of NPI showed a good internal consistency, convergent validity, as well as an excellent inter-rater and test-retest reliability. These results suggested that this version emerges as a promising tool in the evaluation of neuropsychiatric symptoms in institutionalized elderly people.

However, additional research is recommended with samples recruited from other settings for further validation of these results, to analyze other psychometric proprieties of the present version.

Acknowledgement

The authors wish to thank the board of institutions, clinical staff and all residents for their collaboration. Statistical analysis was sponsored by Novartis Farma.

Conflict of Interest

None.

Authors Contributions

Lia Fernandes participated in the definition and design of the study. Ana Rita Ferreira and Sonia Martins participated in the data collection. Lia Fernandes, Ana Rita Ferreira and Sonia Martins contributed to the writing of the article, analyses and interpretation of the results, as well as, to the critical revision of the article with Orquidea Ribeiro. All authors have approved the final manuscript.


References▴Top 
  1. Alzheimer A, Stelzmann RA, Schnitzlein HN, Murtagh FR. An English translation of Alzheimer's 1907 paper, "Uber eine eigenartige Erkankung der Hirnrinde". Clin Anat. 1995;8(6):429-431.
    doi pubmed
  2. Geda YE, Schneider LS, Gitlin LN, Miller DS, Smith GS, Bell J, Evans J, et al. Neuropsychiatric symptoms in Alzheimer's disease: past progress and anticipation of the future. Alzheimers Dement. 2013;9(5):602-608.
    doi pubmed
  3. Finkel SI, Costa e Silva J, Cohen G, Miller S, Sartorius N. Behavioral and psychological signs and symptoms of dementia: a consensus statement on current knowledge and implications for research and treatment. Int Psychogeriatr. 1996;8(Suppl 3):497-500.
    doi pubmed
  4. International Psychogeriatric Association. Behavioral and Psychological Symptoms of Dementia (BPSD). Educational Pack. IPA. 1998. Available at: http://www.ipa-online.net/pdfs/1BPSDfinal.pdf.
  5. Benoit M, Dygai I, Migneco O, Robert PH, Bertogliati C, Darcourt J, Benoliel J, et al. Behavioral and psychological symptoms in Alzheimer's disease. Relation between apathy and regional cerebral perfusion. Dement Geriatr Cogn Disord. 1999;10(6):511-517.
    doi pubmed
  6. Lyketsos CG, Steinberg M, Tschanz JT, Norton MC, Steffens DC, Breitner JC. Mental and behavioral disturbances in dementia: findings from the Cache County Study on Memory in Aging. Am J Psychiatry. 2000;157(5):708-714.
    doi pubmed
  7. Brodaty H, Draper B, Saab D, Low LF, Richards V, Paton H, Lie D. Psychosis, depression and behavioural disturbances in Sydney nursing home residents: prevalence and predictors. Int J Geriatr Psychiatry. 2001;16(5):504-512.
    doi pubmed
  8. Fernandes L. Alteracoes Cognitivas e Comportamentais da Demencia. In: Sociedade Portuguesa de Enfermagem de Saude Mental (SPESM), eds. E-book do III Congresso Internacional da SPESM - “Da Investigacao a Pratica Clinica em Saude Mental”. Capitulo 10. Porto: SPESM. 2012;126-133.
  9. Finkel S. Introduction to behavioural and psychological symptoms of dementia (BPSD). Int J Geriatr Psychiatry. 2000;15(Suppl 1):S2-4.
    doi
  10. Frisoni GB, Rozzini L, Gozzetti A, Binetti G, Zanetti O, Bianchetti A, Trabucchi M, et al. Behavioral syndromes in Alzheimer's disease: description and correlates. Dement Geriatr Cogn Disord. 1999;10(2):130-138.
    doi pubmed
  11. Lopez OL, Becker JT, Sweet RA, Klunk W, Kaufer DI, Saxton J, Habeych M, et al. Psychiatric symptoms vary with the severity of dementia in probable Alzheimer's disease. J Neuropsychiatry Clin Neurosci. 2003;15(3):346-353.
    doi pubmed
  12. Cerejeira J, Lagarto L, Mukaetova-Ladinska EB. Behavioral and psychological symptoms of dementia. Front Neurol. 2012;3:73.
    doi pubmed
  13. Herrmann N, Lanctot KL, Sambrook R, Lesnikova N, Hebert R, McCracken P, Robillard A, et al. The contribution of neuropsychiatric symptoms to the cost of dementia care. Int J Geriatr Psychiatry. 2006;21(10):972-976.
    doi pubmed
  14. Sink KM, Holden KF, Yaffe K. Pharmacological treatment of neuropsychiatric symptoms of dementia: a review of the evidence. JAMA. 2005;293(5):596-608.
    doi pubmed
  15. Katona C, Livingston G, Cooper C, Ames D, Brodaty H, Chiu E. International Psychogeriatric Association consensus statement on defining and measuring treatment benefits in dementia. Int Psychogeriatr. 2007;19(3):345-354.
    doi pubmed
  16. Gauthier S, Cummings J, Ballard C, Brodaty H, Grossberg G, Robert P, Lyketsos C. Management of behavioral problems in Alzheimer's disease. Int Psychogeriatr. 2010;22(3):346-372.
    doi pubmed
  17. Mega MS, Cummings JL, Fiorello T, Gornbein J. The spectrum of behavioral changes in Alzheimer's disease. Neurology. 1996;46(1):130-135.
    doi pubmed
  18. Beeri MS, Werner P, Davidson M, Noy S. The cost of behavioral and psychological symptoms of dementia (BPSD) in community dwelling Alzheimer's disease patients. Int J Geriatr Psychiatry. 2002;17(5):403-408.
    doi pubmed
  19. Tun SM, Murman DL, Long HL, Colenda CC, von Eye A. Predictive validity of neuropsychiatric subgroups on nursing home placement and survival in patients with Alzheimer disease. Am J Geriatr Psychiatry. 2007;15(4):314-327.
    doi pubmed
  20. Geda YE, Roberts RO, Knopman DS, Petersen RC, Christianson TJ, Pankratz VS, Smith GE, et al. Prevalence of neuropsychiatric symptoms in mild cognitive impairment and normal cognitive aging: population-based study. Arch Gen Psychiatry. 2008;65(10):1193-1198.
    doi pubmed
  21. Modrego PJ, Ferrandez J. Depression in patients with mild cognitive impairment increases the risk of developing dementia of Alzheimer type: a prospective cohort study. Arch Neurol. 2004;61(8):1290-1293.
    doi pubmed
  22. Gabryelewicz T, Styczynska M, Luczywek E, Barczak A, Pfeffer A, Androsiuk W, Chodakowska-Zebrowska M, et al. The rate of conversion of mild cognitive impairment to dementia: predictive role of depression. Int J Geriatr Psychiatry. 2007;22(6):563-567.
    doi pubmed
  23. Palmer K, Di Iulio F, Varsi AE, Gianni W, Sancesario G, Caltagirone C, Spalletta G. Neuropsychiatric predictors of progression from amnestic-mild cognitive impairment to Alzheimer's disease: the role of depression and apathy. J Alzheimers Dis. 2010;20(1):175-183.
    pubmed
  24. Cummings JL, Mega M, Gray K, Rosenberg-Thompson S, Carusi DA, Gornbein J. The Neuropsychiatric Inventory: comprehensive assessment of psychopathology in dementia. Neurology. 1994;44(12):2308-2314.
    doi pubmed
  25. Lyketsos CG, Lopez O, Jones B, Fitzpatrick AL, Breitner J, DeKosky S. Prevalence of neuropsychiatric symptoms in dementia and mild cognitive impairment: results from the cardiovascular health study. JAMA. 2002;288(12):1475-1483.
    doi pubmed
  26. Cummings JL, Ihl R, Herrschaft H, Hoerr R, Tribanek M. Sensitivity to change of composite and frequency scores of the Neuropsychiatric Inventory in mild to moderate dementia. Int Psychogeriatr. 2013;25(3):431-438.
    doi pubmed
  27. Levy ML, Miller BL, Cummings JL, Fairbanks LA, Craig A. Alzheimer disease and frontotemporal dementias. Behavioral distinctions. Arch Neurol. 1996;53(7):687-690.
    doi pubmed
  28. Ballard CG, Margallo-Lana M, Fossey J, Reichelt K, Myint P, Potkins D, O'Brien J. A 1-year follow-up study of behavioral and psychological symptoms in dementia among people in care environments. J Clin Psychiatry. 2001;62(8):631-636.
    doi pubmed
  29. Minett TS, Thomas A, Wilkinson LM, Daniel SL, Sanders J, Richardson J, Littlewood E, et al. What happens when donepezil is suddenly withdrawn? An open label trial in dementia with Lewy bodies and Parkinson's disease with dementia. Int J Geriatr Psychiatry. 2003;18(11):988-993.
    doi pubmed
  30. Cummings JL. The Neuropsychiatric Inventory: assessing psychopathology in dementia patients. Neurology. 1997;48(5 Suppl 6):S10-16.
    doi pubmed
  31. Direccao Geral de Saude. Programa nacional para a saude mental: orientacoes programaticas. DGS. 2012. Available at: www.dgs.pt.
  32. 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(3):189-198.
    doi
  33. Guerreiro M, Silva AP, Botelho MA, Leitao O, Castro-Caldas A, Garcia C. Adaptacao a populacao portuguesa da traducao do Mini Mental State Examination (MMSE). Rev Port Neurol. 1994;1(9):9-10.
  34. Sousa LB, Simoes MR, Firmino H. Adults and Older Adults Functional Assessment Inventory (IAFAI): validation studies. Aging Ment Health. 2011;15(Suppl 1):13-14.
  35. Yesavage JA, Brink TL, Rose TL, Lum O, Huang V, Adey M, Leirer VO. Development and validation of a geriatric depression screening scale: a preliminary report. J Psychiatr Res. 1982;17(1):37-49.
    doi
  36. Barreto J, Leuschner A, Santos F, Sobral M. Escala de Depressao Geriatrica. In: Grupo de Estudos de Envelhecimento Cerebral e Demencia (GEECD), eds. Escalas e Testes na Demencia. Lisboa: Novartis, 2003.
  37. Leitao O, Nina A. Inventario Neuropsiquiatrico. In Grupo de Estudos de Envelhecimento Cerebral e Demencia (GEECD), eds. Escalas e Testes na Demencia. Lisboa: Novartis, 2008.
  38. Kaufer DI, Cummings JL, Christine D, Bray T, Castellon S, Masterman D, MacMillan A, et al. Assessing the impact of neuropsychiatric symptoms in Alzheimer's disease: the Neuropsychiatric Inventory Caregiver Distress Scale. J Am Geriatr Soc. 1998;46(2):210-215.
    pubmed
  39. Vilalta-Franch J, Lozano-Gallego M, Hernandez-Ferrandiz M, Llinas-Regla J, Lopez-Pousa S, Lopez OL. [The Neuropsychiatric Inventory. Psychometric properties of its adaptation into Spanish]. Rev Neurol. 1999;29(1):15-19.
    pubmed
  40. Choi SH, Na DL, Kwon HM, Yoon SJ, Jeong JH, Ha CK. The Korean version of the neuropsychiatric inventory: a scoring tool for neuropsychiatric disturbance in dementia patients. J Korean Med Sci. 2000;15(6):609-615.
    doi pubmed
  41. Kat MG, de Jonghe JF, Aalten P, Kalisvaart CJ, Droes RM, Verhey FR. [Neuropsychiatric symptoms of dementia: psychometric aspects of the Dutch Neuropsychiatric Inventory (NPI)]. Tijdschr Gerontol Geriatr. 2002;33(4):150-155.
    pubmed
  42. Politis AM, Mayer LS, Passa M, Maillis A, Lyketsos CG. Validity and reliability of the newly translated Hellenic Neuropsychiatric Inventory (H-NPI) applied to Greek outpatients with Alzheimer's disease: a study of disturbing behaviors among referrals to a memory clinic. Int J Geriatr Psychiatry. 2004;19(3):203-208.
    doi pubmed
  43. Camozzato AL, Kochhann R, Simeoni C, Konrath CA, Pedro Franz A, Carvalho A, Chaves ML. Reliability of the Brazilian Portuguese version of the Neuropsychiatric Inventory (NPI) for patients with Alzheimer's disease and their caregivers. Int Psychogeriatr. 2008;20(2):383-393.
    doi pubmed
  44. Squelard GP, Missotten PA, Paquay L, De Lepeleire J, Buntinx FJ, Fontaine O, Adam SR, et al. Neuropsychiatric Inventory data in a Belgian sample of elderly persons with and without dementia. Clin Interv Aging. 2012;7:423-430.
    doi pubmed
  45. Voyer P, Verreault R, Mengue PN, Morin CM. Prevalence of insomnia and its associated factors in elderly long-term care residents. Arch Gerontol Geriatr. 2006;42(1):1-20.
    doi pubmed
  46. Alessi CA, Schnelle JF. Approach to sleep disorders in the nursing home setting. REVIEW ARTICLE. Sleep Med Rev. 2000;4(1):45-56.
    doi pubmed
  47. Zuidema SU, de Jonghe JF, Verhey FR, Koopmans RT. Environmental correlates of neuropsychiatric symptoms in nursing home patients with dementia. Int J Geriatr Psychiatry. 2010;25(1):14-22.
    pubmed
  48. Zuidema SU, de Jonghe JF, Verhey FR, Koopmans RT. Predictors of neuropsychiatric symptoms in nursing home patients: influence of gender and dementia severity. Int J Geriatr Psychiatry. 2009;24(10):1079-1086.
    doi pubmed
  49. Korner A, Lauritzen L, Lolk A, Abelskov K, Christensen P, Nilsson FM. The Neuropsychiatric Inventory--NPI. Validation of the Danish version. Nord J Psychiatry. 2008;62(6):481-485.
    doi pubmed
  50. Davidsdottir SR, Snaedal J, Karlsdottir G, Atladottir I, Hannesdottir K. Validation of the Icelandic version of the Neuropsychiatric Inventory with Caregiver Distress (NPI-D). Nord J Psychiatry. 2012;66(1):26-32.
    doi pubmed
  51. Wang T, Xiao S, Li X, Wang H, Liu Y, Su N, Fang Y. Reliability and validity of the Chinese version of the neuropsychiatric inventory in mainland China. Int J Geriatr Psychiatry. 2012;27(5):539-544.
    doi pubmed


This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Journal of Clinical Medicine Research is published by Elmer Press Inc.

 

Browse  Journals  

 

Journal of Clinical Medicine Research

Journal of Endocrinology and Metabolism

Journal of Clinical Gynecology and Obstetrics

 

World Journal of Oncology

Gastroenterology Research

Journal of Hematology

 

Journal of Medical Cases

Journal of Current Surgery

Clinical Infection and Immunity

 

Cardiology Research

World Journal of Nephrology and Urology

Cellular and Molecular Medicine Research

 

Journal of Neurology Research

International Journal of Clinical Pediatrics

 

 
       
 

Journal of Clinical Medicine Research, monthly, ISSN 1918-3003 (print), 1918-3011 (online), published by Elmer Press Inc.                     
The content of this site is intended for health care professionals.
This is an open-access journal distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted
non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Creative Commons Attribution license (Attribution-NonCommercial 4.0 International CC-BY-NC 4.0)


This journal follows the International Committee of Medical Journal Editors (ICMJE) recommendations for manuscripts submitted to biomedical journals,
the Committee on Publication Ethics (COPE) guidelines, and the Principles of Transparency and Best Practice in Scholarly Publishing.

website: www.jocmr.org   editorial contact: editor@jocmr.org
Address: 9225 Leslie Street, Suite 201, Richmond Hill, Ontario, L4B 3H6, Canada

© Elmer Press Inc. All Rights Reserved.