Hostname: page-component-cd9895bd7-dk4vv Total loading time: 0 Render date: 2024-12-22T17:25:12.588Z Has data issue: false hasContentIssue false

Subjective and objective dimensions of quality of life in psychiatric patients: A factor analytical approach

The South Verona Outcome Project 4

Published online by Cambridge University Press:  02 January 2018

Mirella Ruggeri*
Affiliation:
Department of Medicine and Public Health, Section of Psychiatry, University of Verona, Italy
Richard Warner
Affiliation:
Mental Health Center of Boulder County, Boulder, Colorado, USA
Giulia Bisoffi
Affiliation:
Department of Medicine and Public Health, Section of Psychiatry, University of Verona, Italy
Laura Fontecedro
Affiliation:
Department of Medicine and Public Health, Section of Psychiatry, University of Verona, Italy
*
Professor Mirella Ruggeri, Dipartimento di Medicina e Sanità Pubblica, Sezione di Psichiatria, Università di Verona, Ospedale Policlinico, 37134 Verona, Italy. Tel: +39 045 807 4441; Fax: +39 045 58 5871; E-mail: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Background

Both subjective and objective information is necessary to assess quality of life (QOL).

Aims

To explore the role of subjective and objective QOL dimensions and their cross-sectional and longitudinal predictors.

Method

The relationship between QOL, as measured by the Lancashire Quality of Life Profile (LQL), and demographic variables, diagnosis, psychopathology, disability, functioning, affect balance, self-esteem, service use and service satisfaction was investigated at two points in time, using factor analysis and multiple regression techniques.

Results

One subjective and two objective LQL factors with strong face validity were identified. Cross-sectional predictors of the subjective factor were primarily subjective measures; longitudinally, few predictors of this factor were identified. The cross-sectional and longitudinal predictors of the objective factors were primarily demographic and observer-rated measures.

Conclusions

Subjective and objective data are distinct types of information. Objective measures may be more suitable in detecting treatment effects. Subjective information is necessary to complete the QOL picture and to enhance the interpretation of objective data.

Type
Papers
Copyright
Copyright © 2001 The Royal College of Psychiatrists 

Quality of life (QOL) assessment has many apparent merits in the measurement of outcome in chronic illness. It can be used to measure incremental improvements rather than complete cure; it takes account of a wide range of aspects of daily living; it places the consumer at the centre of the picture; and it can be used across various disciplines of medicine (Reference Oliver, Huxley and BridgesOliver et al, 1996). In psychiatry, interest in the measurement of QOL was stimulated by the plight of deinstitutionalised individuals with mental illness and by a parallel interest in assessing such dimensions of daily life as personal safety, isolation, poverty and transience of accommodation. The QOL measures have shown success in comparing different populations of people with mental illness in different circumstances and treatment conditions (Reference Lehman, Possidente and HawkerLehman et al, 1986; Reference Kaiser, Priebe and BarrKaiser et al, 1997; Reference Warner and HuxleyWarner & Huxley, 1998; Reference Warner, de Girolamo and BelelliWarner et al, 1998). It remains an open question, however, whether the approach will prove effective in assessing change over time (Reference Barry and ZissiBarry & Zissi, 1997; Reference LehmanLehman, 1999).

Subjective and objective quality of life

There is no single, universally accepted definition of QOL (Reference LauerLauer, 1999). The World Health Organization definition, for example, focuses on the subjective perspective (WHOQOL Group, 1993), whereas other constructs are broader and include objective indicators of health, housing and other material circumstances. According to recent reviews (Reference LauerLauer, 1999), most researchers believe that both subjective and objective information is necessary to the construct.

Complications arise, however, from the finding that the subjective appraisal of life often bears little or no relation to objective life circumstances (Reference Barry and CrosbyBarry & Crosby, 1996; Reference WarnerWarner, 1999). The same objective event may result in opposite evaluations by the same subject depending on his/her perspective at the time of interview (Reference Skantze, Wanke and BlessSkantze et al, 1994). Objective improvements in life circumstances may produce negative subjective responses (Reference LehmanLehman, 1996). Subjective QOL ratings are often higher in people with schizophrenia than affective disorder, although objective circumstances indicate the reverse (Reference Atkinson, Zibin and ChuangAtkinson et al, 1997; Reference Katschnig and AngermeyerKatschnig & Angermeyer, 1997). A weak or moderate association between observer-rated mental health indicators, such as psychopathology, and subjective QOL has been found in various studies (Reference Corrigan and BuicanCorrigan & Buican, 1995; Reference LehmanLehman, 1996; Reference Oliver, Huxley and BridgesOliver et al, 1996; Reference Kaiser, Priebe and BarrKaiser et al, 1997; Reference Ruggeri, Santolini and StegaganoRuggeri et al, 1999).

With such concerns in mind, this study was designed to investigate the relationship between QOL and key mental health indicators both cross-sectionally and over time, with a particular focus on the differential role of subjective and objective QOL dimensions. Specifically, the study investigates the relationship between these two dimensions, as measured by the Lancashire Quality of Life Profile and demographic variables, diagnosis, psychopathology, disability, functioning, service use, service satisfaction, affect balance and self-esteem at two points in time.

METHOD

Design

Data were collected as part of a naturalistic longitudinal study assessing the outcome of care provided by the community-based service of South Verona: the South Verona Outcome Project (Reference Ruggeri, Biggeri and RucciRuggeri et al, 1998). Information was gathered by the primary treating professional, reported by patients themselves using QOL and service satisfaction questionnaires and obtained from the psychiatric case register (PCR). In this study, data gathered from the same cohort in 1994 and 1996/97 (mean follow-up interval=29.96 months, s.d.=5.71), including patients no longer in treatment, were analysed. The study reported here is a factor analysis of responses to a QOL instrument to determine latent QOL constructs, followed by regression analyses to identify determinants of the constructs cross-sectionally and longitudinally.

Area and mental health service

South Verona is a relatively affluent urban area of north-east Italy, with a population of 75 000. The community mental health service (CMHS) provides the main source of care to area residents, and includes in-patient, out-patient, day care and emergency and rehabilitation services. The South Verona PCR, established in 1978 to collect data on all patients seen by the service, includes demographic, diagnostic and service utilisation information (Reference TansellaTansella, 1991).

Subjects

The analysis reported here is based on 285 patients, over age 15, attending the CMHS who completed the assessments of the South Verona Outcome Project (Reference Ruggeri, Biggeri and RucciRuggeri et al, 1998) in October-December 1994; of these, 183 were followed up in 1996/97, including 54 who were no longer in treatment with the agency. Decrease in cohort size was due to death of subjects (n=11), subjects' refusal to participate (n=20) or to complete the interview (n=28) and failure to locate the subject (n=43). After complete description of the study to the patients, written informed consent was obtained.

Measures

Demographic, diagnostic and service utilisation data for the prior year were extracted from the PCR. Diagnoses were based on ICD-10 (World Health Organization, 1992) and grouped in six categories as follows: schizophrenia, severe affective disorder, depression without psychotic symptoms, neurotic and somatoform disorder, personality disorder and other diagnoses. In some analyses a dichotomous classification of psychotic disorder (including schizophrenia and severe affective disorder) versus not psychotic was used (see Table 1 for more details). The clinicians making the diagnoses were specially trained in ICD coding. An exercise performed with the staff of four European case register centres demonstrated this grouping system to be reliable across centres (Reference Sytema, Giel and Ten HornSytema et al, 1989).

Table 1 Characteristics of the cohort (n=183): demographics, diagnosis, psychopathology, disability, functioning, service utilisation and satisfaction with service in 1994 (all independent variables used in the trunk regression analysis are listed)

Demographics
Gender, female (%) 62.3
Age, years, mean (s.d.) 47.1 (15.5)
Marital status, married 39.9
Higher education (%) 22.9
Employment status
Employed (%) 30.6
Unemployed (%) 12.6
Other (retired, homemaker) (%) 56.8
ICD—10 Diagnosis 1
Schizophrenia (%) 27.9
Severe affective disorder (%) 9.8
Depression without psychotic symptoms (%) 33.3
Neurotic and somatoform disorder (%) 12.6
Personality disorder (%) 11.5
Other (%) 4.9
Psychopathology
BPRS total score mean (s.d.) 1.46 (0.41)
Disability
DAS total score, mean (s.d.) 0.72 (0.81)
Functioning
GAF score, mean (s.d.) 61.34 (15.98)
Psychological measures
Affect balance, mean (s.d.) 5.10 (2.69)
Self-esteem, mean (s.d.) 5.95 (3.09)
Service utilisation in prior year
Admitted to psychiatric hospital (%) 18.0
Treatment contacts, mean (s.d.) 46.62 (93.88)
Satisfaction with service
VSSS score, mean (s.d.) 3.96 (0.53)

Service utilisation data included the number, type and place of out-patient contacts, in-patient admissions and day care contacts. Assessments of psychopathology, disability and functioning were made by the primary clinican, a psychiatrist or psychologist, using the Brief Psychiatric Rating Scale (BPRS) expanded version (Reference Ventura, Green and ShanerVentura et al, 1993), eight items from the Social Roles section of the Disability Assessment Schedule (DAS—II; World Health Organization, 1988) and the Global Assessment of Functioning Scale (GAF; Reference Endicott, Spitzer and FleissEndicott et al, 1976). Patients were asked to complete the Lancashire Quality of Life Profile (LQL; Reference Oliver, Huxley and PriebeOliver et al, 1997) and the Verona Service Satisfaction Scale (VSSS; Reference Ruggeri, Dall'Agnola and AgostiniRuggeri et al, 1994). All scales were the official Italian versions. Primary clinicians were trained in the use of the observer-rated scales and achieved interrater reliability of at least 0.70. In the case of self-administered scales, test-retest was performed in a subsample of subjects and this showed good levels of stability. A research worker assisted the patient in completing questionnaires when necessary.

The LQL, developed from Lehman's QOL scale (Reference Oliver, Huxley and PriebeOliver et al, 1997), is a researcher-led questionnaire enquiring about objective life circumstances and subjective life satisfaction in nine domain — work/education, leisure, religion, finances, living situation, legal/safety, family relations, social relations and health — and it includes subjective ratings of overall well-being. The subjective satisfaction ratings are recorded on sevenpoint ‘delighted—terrible’ Likert scales (see Table 2). The measure includes affect balance and self-esteem scales. Construct, content and criterion validity, reliability and internal consistency of the LQL have been demonstrated to be satisfactory (Oliver et al, Reference Oliver, Huxley and Bridges1996, Reference Oliver, Huxley and Priebe1997). To reduce the number of variables in the factor analysis, some objective items in the domains of leisure, social relations and health were combined in three single scales. Where there was more than one satisfaction item in a domain, a mean of all such scores in the domain was completed.

Table 2 Characteristics of the cohort (n=183): subjective and objective components from each domain of the Lancashire Quality of Life Profile in 1994 (all variables used in the factor analysis are listed)

Overall well-being
Mean (s.d.) 4.21 (1.43)
Work/study
Satisfaction, mean (s.d.) 3.99 (1.67)
Time/week, hours, mean (s.d.) 11.7 (16.7)
Earnings/months, thousand lire, mean (s.d.) 486 (753)
Leisure
Satisfaction, mean (s.d.) 4.37 (1.17)
No. leisure items checked for past 2 weeks (max.=4), mean (s.d.) 2.81 (0.83)
Religion
Satisfaction, mean (s.d.) 4.78 (1.35)
No. times attended religious activity in past month, mean (s.d.) 3.48 (4.25)
Financial situation
Satisfaction, mean (s.d.) 3.81 (1.56)
Family income/month, thousand lire, mean (s.d.) 1197 (783)
Living situation
Satisfaction, mean (s.d.) 4.57 (1.15)
Time living in current accommodation, years, mean (s.d.) 17.8 (14.7)
No. other people in household, mean (s.d.) 2.26 (1.35)
Proportion in unsheltered accommodation (%) 89.6
Safety/legal situation
Satisfaction, mean (s.d.) 4.73 (1.32)
% Accused of a crime in past year 3.9
% Victims of violence in past year 10.1
Family relations
Satisfaction, mean (s.d.) 4.67 (1.39)
% With daily family contact 78.4
% Living with family 73.2
Social relations
Satisfaction, mean (s.d.) 4.52 (1.49)
% Who met friend in past week 59.7
No. close personal relations items checked (max.=3), mean (s.d.) 1.53 (1.14)
Health
Satisfaction, mean (s.d.) 4.59 (1.19)
No. physical illness items checked (max.=2), mean (s.d.) 0.87 (0.69)
% With physical disability 18.0
No. physical illness items checked (max.=2), mean (s.d.) 0.87 (0.69)
No. mental illness items checked (max.=3), mean (s.d.) 2.02 (0.71)

Statistical analysis

An exploratory factor analysis (Reference CattellCattell, 1978) was conducted on the LQL scores for 285 patients in the 1994 (Time 1) cohort. The full sample was used in order to maximise the possibility of detecting latent QOL constructs while maintaining an adequate balance of test items to subjects. Twenty-seven items (or subscales) from the LQL (17 objective and 10 subjective) were factor analysed using principal component analysis. To determine how many factors to select, we used the scree test in conjunction with the criterion of interpretability of the factor solution. Three factors were found and rotated using the Varimax method to obtain a clearer pattern of factor loadings (see Table 3). An identical factor analysis was conducted on Time 1 and Time 2 data for the 183 subjects with complete evaluations.

Table 3 Changes over 2 years in subjective and objective domains of the Lancashire Quality of Life Profile (LQL) (n=183)

LQL sub-scale/item Percentage of subjects
Worsened Stable1 Improved
Overall well-being 38.9 19.4 41.7
Work/study satisfaction 36.4 24.7 38.9
Leisure satisfaction 26.4 36.4 37.6
Religion satisfaction 35.5 24.1 40.4
Financial situation satisfaction 34.9 24.6 40.6
Living situation satisfaction 26.7 37.5 35.8
Safety/legal situation satisfaction 35.6 29.9 34.5
Family relations satisfaction 25.9 31.0 43.1
Social relations satisfaction 33.1 29.1 37.7
Health satisfaction 31.6 37.9 30.5
Decreased Stable2 Increased
Working time hours 38.6 49.1 12.3
Earnings/month 16.1 66.4 17.5
Leisure activities 25.7 46.9 27.4
Religious activity 16.1 58.0 25.9
Global income 17.2 70.8 12.0
Met friend in past week 19.3 65.1 15.7
People in household 20.6 65.4 14.0
Personal relations 22.6 46.3 31.1
Living with family 4.0 93.1 2.9
Family contacts 16.7 76.5 6.8
Unsheltered living 2.8 91.6 5.6
Legal problems (being accused of a crime) 3.5 96.0 0.6
Problems with other people (violence) 6.4 86.7 6.9
Problems with physical illness 23.5 52.4 24.1
Problems with physical disability 8.1 79.4 12.5
Problems with mental illness 12.9 64.7 22.4

A multivariate regression analysis of the QOL factor scores from Time 1 was performed and revealed no correlation between the residuals of the three factors, indicating that separate regression of each factor on potential determinants was appropriate.

Three successive block-stratified multiple regression models were constructed with one QOL factor score from Time 1 as dependent variable and a series of Time 1 variables (see Table 1) as independent variables. In the block-stratified procedure, putative determinants, organised into blocks denoting logically homogeneous sets of increasing complexity, were analysed in sequence; a similar method has been used in other studies (UK700 Group, 1999). In each block variables were selected using a stepwise procedure, retaining those variables that were significant in the previous blocks. First, the determinants summarising each block were included as ‘trunk’ variables (e.g. BPRS as a total mean score). Subsequently, each trunk in turn, taking into account the trunk determinants of the previous blocks, was exploded into its ‘branches’ to assess the contribution of each branch: diagnostic groups were assessed separately, BPRS, DAS and VSSS were split into their subscales (BPRS: Anxiety/Depression, Positive symptoms, Negative symptoms, Mania, Cognitive symptoms; DAS: Participation in household, Relationship with partner, Parental role, Friction with social contacts, Occupational role — performances/interest, Interest and information, Behavior in emergencies; VSSS: Professional skills and behavior, Information, Access, Efficacy, Type of intervention, Relatives' involvement) and aspects related to the type (community support, clinical assessment or psychotherapy) and the place (out-patient or casualty department, patient's home, community) of contacts were assessed. This procedure allowed the exploration of the role of the branch variables as determinants, while preserving a satisfactory ratio between the number of cases and variables included in the analysis.

To explore longitudinal effects, a block-straitified multiple regression model, similar to that used for the cross-sectional analyses, was constructed with one QOL factor score from Time 2 as the dependent variable and adding the factor scores from Time 1 to the set of independent variables used in the previous analyses. This model permitted the extraction of the effect of the QOL factor at Time 1 so that its residual could be analysed to explore what variables are associated with the change in QOL, given the baseline levels.

RESULTS

Characteristics of the cohort

Characteristics of the cohort are presented in Table 1. As shown in the table, patients both with and without psychotic symptoms have been included in the study; as expected, a difference between these two groups was found with regard to severity of psychopathology (15.7% of patients had a BPRS mean score ≥ 2 in the group of patients with psychosis v. 5.3% in the group of patients without psychosis; BPRS total mean scores differed significantly, P=0.029, Mann-Whitney U-test), disability (14.3% of patients had a DAS mean score ≥2 in the group of patients with psychosis v. 2.7% in the group of patients without psychosis; DAS total mean scores differed significantly, P <0.001, Mann-Whitney U-test) and dysfunction (27.1% of patients had a GAF score ≤40 in the group of patients with psychosis v. 6.2% in the group of patients without psychosis; GAF mean scores differed significantly, P=0.001, Mann-Whitney U-test). The QOL responses of the cohort are reported in Table 2.

Changes over 2 years in subjective and objective domains of the LQL are reported in Table 3. Overall, an improvement in LQL total mean score of subjective items was found in 26.4% of patients, and a worsening in 19.8%. Over 2 years, an improvement in BPRS total mean score was found in 11.5% of patients, and a worsening in 13.2% (change exceeding ±1/10 of the five-point Likert scale); an improvement in DAS total mean score was found in 26.4% of patients, and a worsening in 16.5% (change exceeding ±1/10 of the ten-point interval scale); an improvement in GAF total score was found in 25.3% of patients, and a worsening in 46.2% (change exceeding ±1/10 of the five-point Likert scale); an improvement in VSSS overall satisfaction score was found in 19.2% of patients, and a worsening in 24.9% (change exceeding ±1/10 of the five-point Likert scale).

Factor analysis

In the factor analysis of the Time 1 sample (n=285), the scree plot confirmed the initial hypothesis that the LQL was multidimensional and revealed three factors with relatively high eigenvalues; with Varimax rotation, three interpretable QOL factors were obtained (see Table 4: subjective satisfaction; objective work/income; and objective living situation/safety. The subjective factor accounted for 17% of the item variance, the objective work/income factor for 9% and the objective living-situation factor for 7%. No items loaded on more than one factor, 22 of the 27 items loaded onto one or another of the three factors. A factor analysis of the Time 1 data for the cohort followed up at Time 2 (n=183) established that the same latent constructs were present in the smaller cohort. Factor analysis of the Time 2 data identified the same three factors, with minor changes.

Table 4 Factor loading matrix for 27 quality of life items loading on three factors: cohort in 1994 (n=285)

Item Factor
Subjective: satisfaction Objective: work/income Objective: living situation
Subjective satisfaction items
Employment situation 0.507 0.213 0.119
Leisure activities 0.730 0.008 0.010
Religion 0.491 -0.247 -0.005
Financial situation 0.549 0.273 0.179
Accommodation 0.692 -0.006 0.203
Safety/legal situation 0.547 0.005 0.149
Family relations 0.645 0.000 0.328
Social relations 0.735 0.003 0.008
Health 0.666 0.003 -0.009
Overall well-being 0.783 0.109 -0.001
Objective: work/leisure/income items
Hours of work/week -0.003 0.643 -0.000
Earnings -0.114 0.869 -0.000
Income -0.009 0.792 0.003
Number of leisure activities 0.153 0.397 -0.320
Objective: living situation/safety items
Time in current accommodation (months) 0.104 -0.007 0.375
Living in unsheltered accommodation 0.003 0.004 0.542
Living with family -0.002 0.144 0.652
Frequency of family contact 0.001 0.007 0.434
Accused of a crime in past year -0.004 0.008 -0.542
Victim of assault in past year -0.176 -0.213 -0.417
Physical disability -0.180 -0.252 -0.470
Number of people living in home -0.009 0.009 -0.328
Not loading on any factor
Frequency religious service attendance 0.258 -0.194 -0.225
Close relations with friends 0.151 0.243 0.004
Contact with friend in past week 0.122 0.235 -0.005
Physical health (objective) -0.182 -0.007 -0.004
Mental health (objective) -0.005 -0.288 -0.009

Cross-sectional analysis

Subjective satisfaction factor

As shown in Table 5, in the regression analysis with trunk variables, older age (3% delta variance), higher satisfaction with services (22%), positive affect (25%) and greater self-esteem (6%) were associated with a higher subjective QOL satisfaction score, accounting for 55% of the variance. When branch variables were entered into the equation, anxiety/depression (BPRS) was found to be negatively associated (7%), mania positively associated (4%), and satisfaction with service efficacy (23%) and access (2%) positively correlated.

Table 5 Cross-sectional and longitudinal predictors for each factor of Lancashire Quality of Life Profile: estimated β coefficients, their significance and delta variance (%) for the final model (Blocks 1+2+3+4+5+6+7)

Dependent variable Cross-sectional analysis: Time 1 Longitudinal analysis: Time 2
Factor 1 Factor 2 Factor 3 Factor 1 Factor 2 Factor 3
Subjective Work Living situation Subjective Work Living situation
Factor 1, Time 1 0.67 (0.00) 42.4% 0.13 (0.02) 2.1%
Factor 2, Time 1 0.48 (0.00) 39.8% 0.23 (0.00) 4.5%
Factor 3, Time 1 0.15 (0.01) 1.4% -0.60 (0.00) 42.6%
Block 1
Gender (female) -0.22 (0.00) 4%
Age (older) 0.11 (0.04) 2.5% -0.37 (0.00) 14.3% -0.21 (0.00) 1.7% 0.13 (0.03) 1.6%
Marital status (married) 0.10 (0.13) 2.5% 0.30 (0.00) 11.5%
Educational level (higher) 0.26 (0.00) 8.1%
Unemployment (v. others) 0.12 (0.03) 1.1% -0.12 (0.04) 1.4%
Block 2
Not psychotic 0.10 (0.07) 1.4%
Block 3
BPRS total score -0.12 (0.08) 2.1%
DAS total score -0.12 (0.10) 4.2%
GAF score 0.13 (0.02) 1.2%
Block 4
Admission to hospital (yes) -0.19 (0.01) 3% -0.11 (0.05) 0.8%
Day-hospital contacts (yes) -0.23 (0.00) 3.7%
Block 5
VSSS total score 0.25 (0.00) 22.1%
Block 6
Affect balance scale 0.31 (0.00) 24.5%
Block 7
Self-esteem scale 0.35 (0.00) 6%
Total % variance explained 55.1% 32.8% 16.6% 43.5% 50.9% 51.6%

Objective work/income/leisure factor

Trunk variables retained after stepwise regression were younger age (14% delta variance), higher education (8%), being married (3%), lower disability (7%) and not attending day care (4%), accounting for 33% of the variance. When branch variables were entered into the equation, not having a diagnosis of personality disorder (2%), low negative symptoms (8%), higher level of interest/information (DAS) (6%), and receiving fewer home visits (4%) were found to be correlated with greater QOL in the work/income factor.

Objective living-situation/safety factor

In the analysis with trunk variables, a more stable, safe and unsheltered living situation was associated with being married (12% delta variance), lower total symptomatology (2%) and not being admitted to hospital (3%), explaining 17% of the variance. When branch variables were introduced into the equation, lower positive symptoms (3%) and lower satisfaction with service efficacy (2%) were correlated with greater QOL in living situation.

Longitudinal analysis

Subjective satisfaction factor

As shown in Table 5, in the regression with trunk variables, the subjective satisfaction factor at Time 1 accounted for 42% of the variance in the same factor at Time 2. Un-employment at Time 1 accounted for an additional 1% of the variance. No branch variable was retained in any of the analyses.

Objective work/income/leisure factor

The score for the work/income factor at Time 1, in the trunk regression analysis, accounted for 40% of the variance in the factor at Time 2. The amount of variance contributed by other variables retained in the model was as follows: living situation factor, 1%; male gender, 4%; lower age, 2%; being employed, 2%; being without psychosis, 2%; and higher functioning, 1%. Branch variables contributing to the variance in subsequent analyses were: not having schizophrenia (3%) or a personality disorder (1%), low cognitive symptoms (1%) and higher work performance or interest in work (DAS) (1%).

Living-situation/safety factor

In the trunk regression analysis, the score for the living-situation/safety factor at Time 1 accounted for 43% of the variance in this factor at Time 2. The amount of variance contributed by other variables retained in the model was as follows: objective work/income factor, 5%; subjective satisfaction factor, 2%; older age, 2%; no hospital admissions, 1%. Branch variables contributing to the variance in subsequent analyses were low cognitive symptoms (2%) and low satisfaction with access (2%).

DISCUSSION

To our knowledge this is the first longitudinal study of QOL in a broadly selected cohort of psychiatric patients and the first using factor analysis. The approach provides an opportunity to focus on the role of subjective and objective dimensions of QOL. Limitations of the study include loss of one-third of the cohort between baseline and follow-up, variation in follow-up interval, the exploratory nature of the analyses and the large number of analyses performed on the same data set.

Latent constructs of quality of life

We identified three latent constructs of QOL in the LQL: subjective satisfaction, objective work/income/leisure and objective living situation/safety. There is face validity to the construction of these factors and to their patterns of prediction by other variables. For example, every satisfaction and well-being item was included in the subjective factor, and its predictors were other subjective measures, such as service satisfaction and affect balance. However, previous work (Reference Kaiser, Priebe and BarrKaiser et al, 1997) has shown that the factorial structure of subjective QOL might differ between schizophrenia out- and in-patients, and, in the group of in-patients, might depend on the length of the hospitalisation; thus, our results should be taken with caution when applied to psychiatric patients who are not living in the community.

Further research is needed in order to understand better why a remarkable amount of variance (67%) remains unaccounted for; however, the robustness of the factor solution is supported by the identification of the same factor for the cohort at two points in time. Previous research, moreover, has shown that subjective QOL is distinct from objective QOL (Reference Skantze, Wanke and BlessSkantze et al, 1994; Reference Atkinson, Zibin and ChuangAtkinson et al, 1997; Reference Warner, de Girolamo and BelelliWarner et al, 1998). In our study, in the work/income factor, employment was grouped with such anticipated consequences as increased earnings and total income, and it is credible that working and increased income can lead to a greater focus on, and capacity for, leisure activities. Family living for people with mental illness has been shown to be associated with objective QOL benefits (Reference Warner, de Girolamo and BelelliWarner et al, 1998). In this study, we found it to be linked, in the living-situation factor, to increased stability of housing, increased family contact and greater personal safety. The predictors of both objective QOL factors were such dimensions as demographics, disability and pathology, operating in the expected direction.

Predictive power of the regression models

There was more predictive power in the cross-sectional regression model for the subjective factor than for either objective factor. Three measures explained more than half of the variance in the subjective factor, whereas only 33% of the variance in the work/income factor and 16% in the living-situation factor were explained. This may be because the objective factors were influenced by social and economic variables, such as the availability of work or housing, which are not in our model (Reference WarnerWarner, 1994). On the other hand, in the longitudinal model, after the baseline effect of the factor was taken into account, the models explained more variance in the objective factors than the subjective factor. Only a further 1% of the variance in the subjective factor was explained, in contrast to 11% and 9%, respectively, in the work/income and living-situation factors. Changes in psychopathology, disability, functioning and satisfaction with services over 2 years have taken place in many subjects. As shown in Table 3, improvement or worsening over 2 years in both subjective and objective QOL have been found in high percentages of subjects, with a trend for higher stability in objective than in subjective QOL. It appears that the usual mental health predictors do not explain much of the change in QOL over time. Either there are no consistent predictors or those that exist are not in our model.

Predictors of subjective quality of life

The fact that subjective and objective components of QOL cluster separately on factor analysis suggests that they measure different underlying constructs. The distinct nature of subjective QOL is highlighted by the fact that most of the predictors of the subjective factor in this study were subjective variables such as service satisfaction, affect balance and self-esteem. In agreement with previous studies (Reference LehmanLehman, 1996; Reference Oliver, Huxley and BridgesOliver et al, 1996; Reference Kaiser, Priebe and BarrKaiser et al, 1997; Reference Ruggeri, Santolini and StegaganoRuggeri et al, 1999) we found subjective QOL to be weekly influenced by the usual observer-rated predictors used in mental health assessment, either cross-sectionally or longitudinally. A few measures of psychopathology were predictors in the cross-sectional analysis, and employment contributed a small proportion (1%) of the variance to the longitudinal model, but the baseline objective factors were not longitudinal predictors of subjective QOL.

It is reasonable to expect, as we found in this study, that affect state and other subjective elements will influence subjective assessment of QOL. Patients with depression, for example, rate their well-being, functioning and living conditions worse than an independent observer and worse than they do themselves when recovered (Reference Morgado, Smith and LecrubierMorgado et al, 1991). In our longitudinal model, however, the influence of affect state and other subjective variables was much reduced. Although affect balance and self-esteem were important determinants of subjective QOL cross-sectionally, they had no further effect on subjective or objective factors longitudinally.

Service satisfaction, which was associated with QOL cross-sectionally, did not predict change in subjective or objective QOL over time. Its most important association, as in previous studies by this group (Ruggeri et al, Reference Ruggeri, Biggeri and Rucci1998, Reference Ruggeri, Santolini and Stegagano1999) was with current satisfaction with life, indicating that both constructs may measure a common attitude towards satisfaction.

Predictors of objective quality of life

Few subjective variables were predictors of the objective factors, either cross-sectionally or longitudinally. We did find that the subjective satisfaction factor at Time 1 was associated with the living-situation factor in the longitudinal model, but observer-rated and demographic variables explained most of the variance in this factor and all of the variance in the other objective factor in both the longitudinal and cross-sectional models.

As noted, most of the determinants of the objective QOL factors, both cross-sectionally and longitudinally, were demographic factors, functioning level and other variables such as diagnosis, psychopathology and admissions to psychiatric hospitals that might be considered proxy measures of severity of illness. Because severity of illness and functional capacity are common targets of mental health services, objective QOL measures may prove to be more responsive than current subjective measures in the assessment of the effect of these interventions. We may find, for example, that variables in the work/income factor (e.g. hours of work, earnings and number of leisure activities) and in the living-situation factor (e.g. freedom from victimisation and tenure of accommodation) will be valuable in the assessment of rehabilitation outcome.

Implications of this study

Given the distinct nature of subjective QOL and its lack of association with standard mental health predictors and outcomes, what is to be its role in outcome assessment? Some QOL researchers consider the individual's perception of his/her circumstances to be the central component of QOL. Their approach has the merit of empowering the consumer and giving him/her a central role in the development of treatment services. Others, frustrated by the lack of correspondence between subjective and objective information, would abandon subjective evaluation (Reference Atkinson, Zibin and ChuangAtkinson et al, 1997). Warner (Reference Warner1999) has addressed this issue using an analogy with an equivalent area in anthropology, the issue of ‘emics’ and ‘etics’, which deals with similar complexities of informants' perceptions of reality v. the views of outside observers. He argues that subjective and objective appraisals are different kinds of data and that both have a role in QOL assessment. We suggest that the subjective dimension is essential in painting a complete picture of the person's life, in explaining patterns of behaviour and in providing the subject's interpretation of the personal impact of objective circumstances. It is clear that various factors make it difficult to build predictive models around subjective outcomes: these include the tendency towards psychological adaptation or ‘response shift’ that can occur over time in the subjective appraisal of a person's current state (and this might explain why in our study the strong association of service's satisfaction with QOL did not hold up for change at Time 2), the multifactorial determinance of subjective outcomes and the diverse reaction of different individuals to the same circumstances.

The predictors used in our study (largely demographic and observer-rated variables) are associated with change in objective circumstances rather than in subjective QOL. A possible explanation for this is that objective measures may prove to be more suitable in detecting the effects of treatment interventions because many interventions are not targeted at improving the subjective QOL of patients. Although the severity of symptoms and functional capacity remains the principal target of mental health services (rather than the patient's subjective QOL), objective information may be more suitable for building predictive models and in the longitudinal assessment of chronic illness.

Clinical Implications and Limitations

CLINICAL IMPLICATIONS

  • Subjective and objective appraisals of quality of life (QOL) are different kinds of data but both have a role in assessment.

  • Cross-sectionally, higher subjective QOL is associated with other subjective measures, such as positive affect, greater self-esteem and higher satisfaction with services, and is uninfluenced by any of the usual observer-rated predictors; the former measures do not have an additional effect in predicting changes in QOL over 2 years.

  • Objective QOL is predicted by demographic and observer-rated variables both cross-sectionally and at follow-up, but little variance is explained by the models.

LIMITATIONS

  • Loss of one-third of the cohort between baseline and follow-up.

  • Exploratory nature of the analyses.

  • Large number of analyses performed on the same data-set.

ACKNOWLEDGEMENTS

The authors are grateful to Doriana Cristofalo for assistance in data management. We are also grateful to the colleagues and the patients who participated in the South Verona Outcome Project, and we specifically thank Rosa Dall'Agnola, Paola Bonizzata, Marco Stegagno, Giuseppe Imperadore, Nazario Santolini, Stylianos Nicolaou and Manuela Benetollo for their contribution in the data collection. We are indebted to Professor Michele Tansella for his generous and continuous support and valuable advice and for helping to revise the manuscript.

Footnotes

Declaration of interest

This study was supported by the Istituto Superiore di Sanità (ISS), Roma, Progetto Nazionale Salute Mentale, with a grant (no.96/QT/50) to M.R.

References

Atkinson, M., Zibin, S. & Chuang, H. (1997) Characterizing quality of life among patients with chronic mental illness: a critical examination of self-report methodology. American Journal of Psychiatry, 154, 99105.Google Scholar
Barry, M. M. & Crosby, C. (1996) Quality of life as an evaluative measure in assessing the impact of community care on people with long-term psychiatric disorders. British Journal of Psychiatry, 168, 210216.Google Scholar
Barry, M. M. & Zissi, A. (1997) Quality of life as an outcome measure in evaluating mental health services: a review of the empirical evidence. Social Psychiatry and Pyschiatric Epidemiology, 32, 3847.CrossRefGoogle ScholarPubMed
Cattell, R.B. (1978) The Scientific Use of Factor Analysis in Behavior and Life Sciences. New York: Plenum Press.Google Scholar
Corrigan, P. W. & Buican, B. (1995) The construct validity of subjective quality of life for the severely mentally ill. Journal of Nervous and Mental Disease, 183, 281285.Google Scholar
Endicott, J., Spitzer, R. L., Fleiss, J. L., et al (1976) The Global Assessment Scale: a procedure for measuring overall severity of psychiatric disturbance. Archives of General Pscyhiatry, 33, 766771.Google Scholar
Kaiser, W., Priebe, S., Barr, W., et al (1997) Profiles of subjective quality of life in schizophrenic in- and out-patient samples. Psychiatry Research, 66, 153166.Google Scholar
Katschnig, H. & Angermeyer, M. C. (1997) Quality of life in depression. In Quality of Life in Mental Disorders (eds H. Katschnig, H. Freeman, & N. Sartorius), pp. 137147. Chichester: John Wiley & Sons.Google Scholar
Lauer, G. (1999) Concepts of quality of life in mental health care. In Quality of Life and Mental Health Care (eds S. Priebe, J. P. J. Oliver & W. Kaiser), pp. 1934. Philadelphia, PA: Wrightson Biomedical.Google Scholar
Lehman, A. F. (1996) Measures of quality of life among persons with severe and persistent mental disorders. In Mental Health Outcome Measures (eds G. Thornicroft & M. Tansella), pp. 7592. Berlin: Springer CrossRefGoogle Scholar
Lehman, A. F. (1999) Future research in quality of life in mental health care. In Quality of Life and Mental Health Care (eds S. Priebe, J. P. J. Oliver & W. Kaiser), pp. 118. Philadelphia: Wrightson Biomedical.Google Scholar
Lehman, A. F., Possidente, S. & Hawker, F. (1986) The quality of life of chronic patients in a state hospital and in community life. Hospital and Community Psychiatry, 37, 901907.Google Scholar
Morgado, A., Smith, M., Lecrubier, Y., et al (1991) Depressed subjects unwittingly overreport poor social adjustment which they reappraise when recovered. Journal of Nervous and Mental Disease, 179, 614619.Google Scholar
Oliver, J. P. J., Huxley, P. J., Bridges, K., et al (1996) Quality of Life and Mental Health Services. London: Routledge.Google Scholar
Oliver, J. P. J., Huxley, P. J., Priebe, S., et al (1997) Measuring the quality of life of severely mentally ill people using the Lancashire Quality of Life Profile. Social Psychiatry and Psychiatric Epidemiology, 32, 7683.Google Scholar
Ruggeri, M., Dall'Agnola, R., Agostini, C., et al (1994) Acceptability, sensitivity and content validity of VECS and VSSS in measuring expectation and satisfaction in psychiatric patients and their relatives. Social Psychiatry and Psychiatric Epidemiology, 29, 265276.Google Scholar
Ruggeri, M., Biggeri, A., Rucci, P., et al (1998) Multivariate analysis of outcome of mental health care using graphical chain models. Psychological Medicine, 28, 14211431.Google Scholar
Ruggeri, M., Santolini, N., Stegagano, M., et al (1999) La Qualità di Vita dei Pazienti Psichiatrici. In Epidemiologia e Psichiatria Sociale, Monograph Supplement 4. Roma: II Pensiero Scientifico Editore.Google Scholar
Skantze, K., Wanke, M. & Bless, H. (1994) Subjective assessments and evaluations of change: some lessons from social cognition research. In European Review of Social Psychology (eds W. Stroebe & M. Hewstone), pp. 181210. New York: John Wiley & Sons.Google Scholar
Sytema, S., Giel, R., Ten Horn, G.H.M.M., et al (1989) The reliability of diagnostic coding in psychiatric case registers. Psychological Medicine, 9, 9991006.Google Scholar
Tansella, M., (ed.) (1991) Community-based psychiatry. Long-term patterns of care in South Verona. In Psychological Medicine, Monograph Supplement 19. Cambridge: Cambridge University Press.Google Scholar
UK700 Group (1999) Predictors of quality of life in people with severe mental illness. Study methodology with baseline analysis in the UK700 trial. British Journal of Psychiatry, 175, 426432.Google Scholar
Ventura, J., Green, M. F., Shaner, A., et al (1993) Training and quality assurance with the Brief Psychiatric Rating Scale: ‘The drift busters’. International Journal of Methods in Psychiatric Research, 3, 221244.Google Scholar
Warner, R. (1994) Recovery from Schizophrenia. London: Routledge.Google Scholar
Warner, R. (1999) The emics and etics of quality of life assessment. Social Psychiatry and Psychiatric Epidemiology, 34, 117121.Google Scholar
Warner, R. & Huxley, P. (1998) Outcome for people with schizophrenia before and after Medicaid capitation at a community mental health center in Colorado. Psychiatric Services, 49, 802807.Google Scholar
Warner, R., de Girolamo, G., Belelli, G., et al (1998) The quality of life of people with schizophrenia in Boulder, Colorado, and Bologna, Italy. Schizophrenia Bulletin, 24, 559568.Google Scholar
World Health Organization (1988) Disability Assessment Schedule (DAS–II). Geneva: WHO.Google Scholar
World Health Organization (1992) The ICD–10 Classification of Mental and Behavioural Disorders: Clinical Descriptions and Diagnostic Guidelines. Geneva: WHO Google Scholar
WHOQOL Group (1993) Measuring Quality of Life: The Development of the World Health Organization Quality of Life Instrument (WHOQOL). Geneva: WHO.Google Scholar
Figure 0

Table 1 Characteristics of the cohort (n=183): demographics, diagnosis, psychopathology, disability, functioning, service utilisation and satisfaction with service in 1994 (all independent variables used in the trunk regression analysis are listed)

Figure 1

Table 2 Characteristics of the cohort (n=183): subjective and objective components from each domain of the Lancashire Quality of Life Profile in 1994 (all variables used in the factor analysis are listed)

Figure 2

Table 3 Changes over 2 years in subjective and objective domains of the Lancashire Quality of Life Profile (LQL) (n=183)

Figure 3

Table 4 Factor loading matrix for 27 quality of life items loading on three factors: cohort in 1994 (n=285)

Figure 4

Table 5 Cross-sectional and longitudinal predictors for each factor of Lancashire Quality of Life Profile: estimated β coefficients, their significance and delta variance (%) for the final model (Blocks 1+2+3+4+5+6+7)

Submit a response

eLetters

No eLetters have been published for this article.