Skip to main content
Full access
Article
Published Online: 1 March 2006

Subjective Life Satisfaction and Living Situations of Persons in Finland With Long-Term Schizophrenia

Abstract

OBJECTIVE: This study measured subjective life satisfaction among patients with long-term schizophrenia who were living in the community. METHODS: A representative national sample of 2,221 persons with schizophrenia who were discharged from psychiatric hospitals in Finland in 1986, 1990, and 1994 were interviewed three years after discharge. Subjective life satisfaction was measured; patients were asked about their current level of satisfaction and the level of satisfaction they recalled having at the time of discharge. RESULTS: Patients tended to report more satisfaction at follow-up if they were female, had good psychosocial functioning, had several confidants, or were living in group homes or dormitories. Patients tended to be less satisfied at follow-up if they were divorced or had mental and physical symptoms. Patients with depressive symptoms or with low psychosocial functioning and those who were currently hospitalized reported the smallest changes in levels of satisfaction between the two time points. Patients with low psychosocial functioning who were living with their parents, in group homes or dormitories, or in institutions were relatively satisfied, whereas patients with good psychosocial functioning were more satisfied if they lived with their spouse or partner. CONCLUSIONS: Being female and having good psychosocial functioning, confidants, good physical health, and living arrangements in the community that offer support corresponding to the patient's psychosocial state are important factors of life satisfaction among patients with long-term schizophrenia.
Several instruments can measure quality of life among psychiatric patients (1). Most of them include both objective and subjective measures of functional status (2,3), subjective life satisfaction being the minimum and essential component of quality of life (1). Evidence shows that clinically compliant and stable patients with schizophrenia can evaluate and report their quality of life with a high degree of reliability and concurrent validity, which implies that self-report measures are potentially useful tools in clinical trials and outcome studies (4).
Persons with schizophrenia usually rate their life satisfaction higher than persons with other psychiatric disorders (3,5,6). Among patients with schizophrenia, severity of psychopathology, especially the number of negative symptoms, correlates negatively with subjective life satisfaction but not with objective aspects of quality of life (2,7,8). Results concerning functional ability are inconsistent. Arns and Linney (9) found no correlation between functional skills and life satisfaction among patients with severe mental disorders, whereas another study found that functional impairment had an indirect effect on life satisfaction among older patients with schizophrenia (10).
Most of the studies of life satisfaction among patients with schizophrenia have been based on selected and small samples. Because of the types of samples used, it is possible that the studies did not find associations between life satisfaction and basic demographic factors or living situation. For example, Bengtsson-Tops and Hansson (2) found only a weak association between sociodemographic indicators and self-assessed quality of life among 120 patients with schizophrenia. Because of the many changes that the rapid deinstitutionalization process has had on our psychiatric treatment system (11), it is especially important to know which factors are associated with satisfaction among persons with schizophrenia who are living in the community.
The aim of our study was to explore the levels of life satisfaction among patients in Finland with schizophrenia who were discharged from hospitals into the community and the factors associated with their satisfaction. Data were obtained from the Discharged Schizophrenic Patients project, a national project.

Methods

Sample

The study protocol was approved by the ethical committee of Tampere University Hospital in Finland, and all participants gave their written informed consent. The study sample comprised three samples of patients with schizophrenia, aged 15 to 64 years, who were discharged from the psychiatric hospitals in 20 mental health and health care districts in Finland in 1986, 1990, and 1994. The districts have a total population of about four million (the total population of Finland is about five million). The demographic structure, the socioeconomic situation of the population, and the health care services available in the study districts were comparable to those found in the whole country (11). Within each district, patients with schizophrenia who were consecutively discharged from the psychiatric hospitals of the catchment areas after January 1 of each year of study were included, until the samples consisted of 30 patients per 100,000 persons in the general population.
The sampling procedure was based on the hospital discharge registers: the required number of consecutive patients was selected from among the patients with a diagnosis of functional psychosis (based on ICD-8 classification in 1986 and DSM-III-R classification in 1990 and 1994). The researcher-physicians in each district reviewed the case records, reassigned diagnoses to the patients, and subclassified their diagnoses by using the 1987 Finnish Disease Classification (12), which is based on DSM-III-R criteria. Patients were included only if they had schizophrenic disorders only (disorganized, 2951; catatonic, 2952; paranoid, 2953; residual, 2956; and undifferentiated, 2959). Patients with schizoaffective and schizophreniform disorders were excluded. A total of 3,256 patients were included in the study.

Measures

By using all psychiatric case records, data were collected on the patients' background, psychiatric history, living situation and care after discharge, and use of services during the three years before and after discharge. Data concerning the patients' global psychosocial functioning (13), somatic health, working ability, life satisfaction, and medication at discharge were also collected.
Patients were interviewed three years after their hospital discharge. The interviews were conducted by each district's psychiatric team and used a structured interview schedule specifically designed for the study presented here. It included well-defined questions about the patient's clinical and functional state, including the Global Assessment Scale (GAS) (13) and global assessments of the patient's psychotic, neurotic, and depressive symptoms (none, mild, moderate, temporarily severe, or continuously severe); personal relationships; disturbances in social behavior; use of and need for various psychiatric, medical, and social services, including a detailed list of various services and treatments; and satisfaction with psychiatric care. Of the 3,257 patients, 2,232 (68.5 percent) were personally interviewed, and 146 (4.5 percent) were examined by interviews of relatives or staff members. In 255 cases (7.8 percent), the teams were not able to locate the patient. A total of 452 patients (13.9 percent) refused to participate in the interview, and 172 (5.3 percent) had died before the interview. The sampling procedure and methods have been described in detail in previous reports (11,14,15,16).
In a separate section of the interview, patients were asked, "How satisfied are you with your present life situation?" (satisfaction at follow-up; SAF) and "How satisfied were you with your life situation at the time you were discharged from the hospital three years ago?" (satisfaction at discharge; SAD). A visual analogue scale was used to measure satisfaction. Satisfaction was rated from 1, extremely poor, to 10, extremely good. To describe any change during the three-year follow-up period, the difference in satisfaction levels (SDI) was calculated (SAF—SAD).

Statistical analysis

The associations between the dependent and independent variables were analyzed by one-way and two-way analyses of variance (ANOVAs) and by Pearson correlation coefficients. In logistic regression analyses, satisfaction scores were categorized as nonsatisfied, 0, or as satisfied, 1, and the difference in satisfaction was categorized as SDI scores as decreased, 0, or as increased, 1. Forward stepwise logistic regression analysis was used. The variables shown in Table 1 are the independent variables. Data were analyzed with SPSS for Windows, version 10.0. A p value below .05 was considered statistically significant.

Results

Sample

Satisfaction at both time points was adequately measured for 2,221 of the 2,232 patients who were interviewed (99.5 percent). The sociodemographic background characteristics and clinical history of these patients are shown in Table 1. These data represent the independent variables. In terms of sociodemographic background factors, no statistically significant differences were found between the patients who were interviewed at the three-year follow-up and those who were not. However, at the time of discharge, the global psycho-functional ability (as measured by GAS) was poorer among the patients who were interviewed at the follow-up, compared with those who were not. Also, patients who were interviewed at the three-year follow-up used psychiatric services to a greater extent both before and after discharge.
In this study, the two measures of satisfaction—SAD (mean±SD score of 5.52±2.36) and SAF (mean score of 6.95±2.12)—and the difference between these two measures—SDI (mean score of 1.43±2.59)—were used as dependent variables. By using the score closest to the means, patients were divided into two groups: nonsatisfied (SAD score of 0 to 5 [1,089 patients, or 48.9 percent] or a SAF score of 0 to 7 [1,233 patients, or 54.9 percent]) and satisfied (SAD score of 6 to 10 [1,136 patients, or 51.1 percent] or a SAF score of 8 to 10 [1,013 patients, or 45.1 percent]). Additionally, patients were divided according to whether they had experienced a decrease or an increase in satisfaction over the study period (SDI score of -10 to -1 [353 patients, or 15.9 percent] or an SDI score of 1 to 10 [1,365 patients, or 61.5 percent]. The remaining 503 patients (22.6 percent) had experienced no change (SDI score of 0), and they were excluded from logistic regression analyses in which SDI was a dependent variable.

Bivariate analyses

SAD, SAF, and SDI scores, according to the patients' sociodemographic and clinical background, are shown in Table 1. Patients discharged in 1994 were more satisfied than those discharged earlier. Women had higher SAF and SDI scores than men. Age was associated with SAD and SDI scores but not with SAF scores. Compared with older patients, younger patients reported less satisfaction at discharge and had thus experienced more positive changes. Marital status at the three-year follow-up was associated with both SAF and SAD scores. Married patients reported high satisfaction both at discharge and at follow-up, and widowed patients reported high satisfaction at discharge. Patients with a higher level of education had lower SAD scores and higher SDI scores—that is, they had experienced more positive changes than those with less education.
Patients with a shorter duration of illness reported more positive changes, compared with those with a longer duration. Diagnostic subgrouping (not shown in the table) was not associated with satisfaction scores. As expected, GAS scores at follow-up were associated with SAF, SAD, and SDI scores. Patients with lower GAS scores expressed lower satisfaction at follow-up, remembered their satisfaction at discharge as being relatively higher, and had experienced fewer positive changes than patients with higher GAS scores. The corresponding correlations with SAF, SAD, and SDI scores were r=.213 (p<.001), r=-.072 (p=.001) and r=.244 (p<.001), respectively. As can be seen, the correlation between GAS and SAD scores was very low.
SAF scores were negatively correlated with psychotic (r=-.142, p<.001), neurotic (r=-.197, p<.001), and depressive symptoms (r=-.273, p<.001), whereas SAD scores were negatively but very weakly correlated with neurotic (r=-.089, p<.001) and depressive symptoms (r=-.097, p<.001). SDI scores were correlated negatively with psychotic (r=-.115, p<.001), neurotic (r=-.084, p<.001), and depressive symptoms (r=-.137, p<.001).
Patients with severe physical illness had lower SAF and SDI scores. Interestingly, patients with physical symptoms but without any diagnosed physical illness also had low SAF and SDI scores. Patients hospitalized at follow-up had higher SAD scores but lower SAF and SDI scores. This finding indicates that currently hospitalized patients remembered their life situation at the time of discharge as being relatively good, but at the time of examination they were dissatisfied and had experienced more negative changes during the follow-up period.
Living situation at follow-up was associated with SAF and SDI scores but not with SAD scores. Patients who lived with their spouse, in group homes or dormitories, or in another or a temporary housing arrangement were more satisfied than patients who lived alone, with their parents, with another person, or in an institution. GAS scores interacted with housing situation (F=2.16, df=12, 2,197, p=.011). Thus SAF scores were calculated for patients with low GAS scores (score of 0 to 3) and for those with high GAS scores (score of 6 to 10), according to living situation (Figure 1). Patients with low psychosocial functioning had relatively high satisfaction if they lived with their parents, in group homes or dormitories, or in institutions (F=2.26, df=6, 540, p=.037), whereas patients with good psychosocial functioning were less satisfied if they lived with their parents (F=2.77, df=6, 557, p=.012).

Multivariate analyses

Results of logistic regression analyses are shown in Table 2. Discharge year, gender, marital status, number of confidants, and physical health as well as GAS scores and depressive symptoms were statistically significant predictors of SAF scores. Women and patients with several confidants, with good psychosocial functioning (GAS), and without depressive symptoms expressed high satisfaction, whereas divorced or separated patients and those with several physical symptoms were dissatisfied.
When GAS scores and symptoms of mental illness were omitted from the analysis, the other explanatory variables shown in Table 1 remained in the model. When discharge year was also omitted from the analysis, living situation entered into the model. This finding was analyzed more closely in the ANOVA in which SAF scores were explained by discharge year and living situation. This analysis showed that the effect of living situation remained significant (F=3.07, df=6, 2,224, p=.005), whereas the effect of discharge year was no longer significant. Thus categorization of SAF scores meant that living situation lost its effect at the expense of discharge year.
SAD scores were explained by marital status, duration of illness, and treatment situation. Compared with their reference groups, married patients, patients with a long duration of illness, and currently hospitalized patients scored their satisfaction at discharge as being higher. Interestingly, patients with poor psychosocial functioning (as measured by GAS scores) and few symptoms of mental illness (psychotic, neurotic, and depressive) had high satisfaction scores at discharge. When GAS scores and symptoms were omitted from the analysis, the other explanatory variables shown in Table 1 remained in the model.
SDI scores were significantly explained only by treatment situation, GAS scores, and depressive symptoms. Compared with the reference groups, currently hospitalized patients, patients with poor psychosocial functioning, and those with more depressive symptoms had experienced more negative changes in satisfaction. When GAS scores and depressive symptoms were omitted from the analysis, in addition to treatment situation, being hospitalized (odds ratio [OR]=.40, 95 percent confidence interval [CI]=.27 to .62, p<.001), the number of confidants (three or more, OR=1.67, CI=1.05 to 2.65, p=.030) and physical health (having symptoms, OR=.72, CI=.54 to .97, p=.031) also entered into the model.

Discussion

The sample consisted of patients with schizophrenia as defined by DSM-III-R who were discharged from psychiatric hospitals in Finland at baseline. The patients had been ill for an average of about 15 years, and about 90 percent of them were receiving disability payments because of their illness at follow-up (16,17). Compared with patients who were not interviewed at the three-year follow-up, those who were interviewed had been more disturbed at discharge and had used psychiatric services more often both before and, in particular, after discharge. These findings indicate that the sample represents severely disabled patients and that the results of this study can be generalized to patients with long-term schizophrenia. The large study sample reported on here represents patients with schizophrenia who were discharged from hospitals throughout Finland, and thus the sample gives a more general view of patients' satisfaction than local samples.
The major findings of this study were that gender, number of confidants, symptoms of mental illness, and psychosocial functioning were the major determinants of subjective life satisfaction among patients with schizophrenia. Global assessments of psychotic, neurotic, and depressive symptoms represent the level of psychopathology and GAS scores represent the level of functioning, although the GAS also assesses symptoms of mental illness. Many other studies have shown that the psychopathology of patients correlates with life satisfaction (2,3,8,18). On the other hand, the good psychosocial outcomes of female patients with schizophrenia (19,20,21,22,23,24) could explain why female patients in our study were more satisfied than male patients. However, our study showed that symptoms of mental illness and current psychosocial level of functioning do not explain gender differences in life satisfaction; independently of these assessments, women were more satisfied with their life than men.
In addition to gender, the number of close friends or confidants was strongly associated with greater life satisfaction, even when the effects of symptoms of mental illness and psychosocial status were controlled for. This finding has also been shown in other studies (25). This finding demonstrates that patients who were able to create and maintain close interpersonal relationships were the most satisfied with their lives. Close interpersonal relationships thus seem to act as a gender-independent factor in life satisfaction. Roder-Wanner and colleagues (26) found that, although the women in their study did not have more social contacts than men, the number of contacts with friends explained satisfaction with life in both genders.
It is interesting that no significant associations were found between age or duration of illness and life satisfaction at follow-up. Instead, younger patients who had usually been ill for a short time reported low satisfaction at the time of discharge and had, therefore, experienced more positive changes than older patients who had experienced a long duration of illness. This finding may mean that (younger) patients with a short duration of illness actually experienced hospitalization as being worse, compared with older patients who had already had more frequent and longer hospitalizations. It is possible that, compared with older patients, younger patients' expectations regarding their life were higher; therefore, hospitalization was experienced by them as being more unsatisfactory. Older patients were used to their chronic illness, and their expectations were presumably lower.
Compared with patients with less education, the better-educated patients who were younger and had a shorter history of illness reported less satisfaction at the time of discharge, but when the analyses controlled for duration of illness, this association was no longer significant. Thus education seems not to be independently associated with satisfaction. Also, it is plausible that better-educated patients had higher expectations of their life; therefore, hospitalization had a more damaging effect on their levels of satisfaction.
In the study reported here, not only the mental state and psychosocial functioning but also the physical state was an important factor associated with life satisfaction. Physical illnesses are prevalent among patients with schizophrenia (27,28) and can thus decrease patients' life satisfaction. In addition, the occurrence of physical symptoms without a diagnosed illness was associated with low satisfaction, which may be a reflection of the uncertainty that such symptoms produce. Hansson and colleagues (25) also found that satisfaction with health was the major factor associated with subjective quality of life. Careful physical examination and treatment of the physical illnesses of patients with schizophrenia are also important from the point of view of patients' life satisfaction.
Patients who were living in the community were more satisfied than hospitalized patients, and this finding was not explained by other factors, such as gender, mental state, or psychosocial functioning. Compared with patients who were living in the community, currently hospitalized patients remembered their life situation at discharge as exceptionally good, emphasizing their willingness to leave the hospital. Interestingly, patients who were living in group homes or dormitories were the most satisfied.
When the life satisfaction variable was categorized in the multivariate analysis, the association between current life satisfaction and living situation disappeared, whereas an association between life satisfaction, and discharge year appeared. However, in the ANOVA, living situation had a significant effect on current life satisfaction but discharge year did not. This discrepancy is explained by the fact that after 1990 the number of patients living with their parents (low satisfaction) decreased and the number of those living in group homes and dormitories (high satisfaction) increased (16). We believe that the effect of discharge year on current life satisfaction was caused mostly by changes in patients' psychosocial situation. Together, these findings indicate that rather severely disabled patients with schizophrenia prefer living outside of hospitals in accommodations that offer more support than, for example, visiting outpatient clinics or day centers.
The association between life satisfaction and living situation seems to be dependent on the patient's psychosocial functioning. Patients who have poor psychosocial functioning need more daily support, and those who were living with their parents, in group homes or dormitories, or in a hospital expressed relatively high satisfaction. It is likely that their original home, their own parents, staffed group homes or dormitories, and even hospitals can offer the support and security that patients miss when their own mental state and functioning are very limited. However, this type of living situation also means that the burden or stress on the patient's family members is high; therefore, they need support from the psychiatric care system (29).
Among patients with good functioning the situation was different. Among this group, those who lived with their spouse were the most satisfied, whereas those who lived with their parents were the least satisfied. Dependence on parents may be one reason for these patients' dissatisfaction, which could be reversed if they had the option of living more independently or were given support to live that way. Providing such a living situation is a challenge for the local community. It is worth noting that even currently hospitalized patients with good functioning expressed higher satisfaction than those who were living with their parents. In these cases, hospitalization may be temporary and patients will return to the community. Finally, living in group homes or dormitories had an independent positive effect on life satisfaction. Among patients with long-term schizophrenia, this kind of living arrangement seems to be relatively satisfactory, especially if patients do not have a spouse or a partner.
This sample of patients was extensive, and the response rate was good. The study sample represents adequately the population of patients discharged from mental hospitals in the whole country, so the results can be generalized to the whole population of patients in Finland with long-term schizophrenia. However, this study has limitations related to the study design and data collection. Because of the retrospective study design, conclusions about changes in life satisfaction should be drawn with caution. The question "How satisfied were you with your life situation at the time you were discharged from hospital three years ago?" asked for the patient's recall of the situation three years earlier. However, discharge from the hospital acted as an anchor point, which possibly made it easier to recollect the actual feelings of satisfaction. Although assessment of satisfaction at the time of discharge should be seen in the light of the study methods, the assessments give us important information about changes in life satisfaction and the patients' perspective on their life.
We used only one scale for measuring life satisfaction, and various dimensions of life satisfaction may not have been covered. The visual analogue scale is a simple technique for measuring subjective phenomena, and it has been shown to be reliable and valid in most circumstances (30,31). Accordingly, it proved to be easy for the patients in our sample to understand. As an indicator of mental state, we used global assessment of psychotic, neurotic, and depressive symptoms and the GAS, which, in addition to psychosocial functioning, includes a global assessment of psychopathology. A more detailed and standardized description of patients' symptoms would have permitted closer study of the associations between psychopathology and life satisfaction in schizophrenia. However, we believe that global assessment of major symptom groups and GAS scores substantially controlled the effect of symptoms on satisfaction.

Conclusions

In accordance with other studies, being female and having close friends or confidants were major determinants of subjective life satisfaction among patients with schizophrenia. This finding is not explained by patients' psychopathology or psychosocial functioning, although they also had a direct association with current life satisfaction. In addition to psychosocial functioning, physical state was associated with life satisfaction. Thus, in the comprehensive treatment of patients with long-term schizophrenia, patients' physical illnesses must also be taken into account.
We saw a clear trend that patients who were living in the community had greater life satisfaction and reported more positive changes in their life satisfaction than currently hospitalized patients, and this finding was not explained by other factors. Instead, living situation and psychosocial functioning seemed to have an interactive effect on life satisfaction. Among patients whose psychosocial functioning was poor, those who were living in protected conditions (with their parents, in group homes or dormitories, or in hospitals) expressed relatively high satisfaction. On the other hand, among patients with good psychosocial functioning, those who were living with their spouse were the most satisfied and those who were living with their parents were the least satisfied.

Acknowledgments

The authors are grateful to the National Board of Health, the Association of Finnish Mental Hospitals, the League of Hospitals in Finland, and the Academy of Finland for financial support.
Figure 1. Life satisfaction mean scores three years after hospital discharge among 2,221 patients with schizophrenia in Finland, by psychosocial state and living situationa
a Psychosocial functioning was assessed with the Global Assessment Scale (GAS). Poor functioning was indicated by scores that ranged from 0 to 3, and good functioning was indicated by scores that ranged from 6 to 10.
Table 1. Sociodemographic background, clinical data, and satisfaction levels at discharge and three years after discharge and the difference in satisfaction levels among 2,221 patients with schizophrenia in Finlanda
a Not all data were available for all participants.
Table 2. Logistic regression analyses of satisfaction scores at discharge and three years after discharge and the difference in satisfaction levels among 2,221 patients with schizophrenia in Finlanda
a Only significant factors left in the model are reported.

Footnote

Dr. Salokangas is affiliated with the department of psychiatry at the University of Turku and with the Turku Psychiatric Clinic in Finland. Dr. Honkonen is with the Finnish Institute of Occupational Health in Helsinki. Dr. Stengård is with the National Research and Development Centre for Welfare and Health in Helsinki. Ms. Koivisto is with the Tampere School of Public Health at the University of Tampere. Send correspondence to Dr. Salokangas at Kiinamyllynkatu 4-8, Turku, FIN-20520, Finland (e-mail, [email protected]).

References

1.
Lehman A: Measures of quality of life among persons with severe and persistent mental disorders. Social Psychiatry and Psychiatric Epidemiology 31:78–88,1996
2.
Bengtsson-Tops A, Hansson L: Subjective quality of life in schizophrenic patients living in the community: relationship to clinical and social characteristics. European Journal of Psychiatry 14:256–263,1999
3.
Atkinson M, Zibin S, Chuang H: Characterizing quality of life among patients with chronic mental illness: a critical examination of the self-report methodology. American Journal of Psychiatry 154:99–105,1997
4.
Voruganti N, Heslegrave RJ, Awad AG, et al: Quality of life measurement in schizophrenia: reconciling the quest for subjectivity with the question of reliability. Psychological Medicine 28:165–172,1998
5.
Koivumaa-Honkanen HT, Honkanen R, Antikainen R, et al: Self-reported life satisfaction and treatment factors in patients with schizophrenia, major depression, and anxiety disorder. Acta Psychiatrica Scandinavica 99:377–384,1999
6.
Rohland BM, Langbehn DR, Rohrer JE: Relationship between service effectiveness and satisfaction among persons receiving Medicaid mental health services. Psychiatric Services 51:248–250,2000
7.
Packer S, Husted J, Cohen S, et al: Psychopathology and quality of life in schizophrenia. Journal of Psychiatry and Neuroscience 22:231–234,1997
8.
Ho BC, Nopoulos P, Flaum M, et al: Two-year outcome in first-episode schizophrenia: predictive value of symptoms for quality of life. American Journal of Psychiatry 155:1196–1201,1998
9.
Arns PG, Linney JA: Relating functional skills of severely mentally ill clients to subjective and societal benefits. Psychiatric Services 46:260–265,1995
10.
Cohen CI, Talavera N: Functional impairment in older schizophrenic persons: toward a conceptual model. American Journal of Geriatric Psychiatry 8:237–244,2000
11.
Salokangas RKR, Saarinen S: Deinstitutionalization and schizophrenia in Finland: discharged patients and their care: a follow-up study of schizophrenic patients discharged from Finnish mental hospitals in 1982, 1986, and 1990. Schizophrenia Bulletin 24:457–467,1998
12.
Tautiluokitus 1987 [Classification of diseases 1987]. Lääkintöhallitus [National Board of Health in Finland], Helsinki, Valtion painatuskeskus [Printing Center of State], 1986
13.
Endicott J, Spitzer RL, Fleis JL, et al: The Global Assessment Scale: a procedure for measuring overall severity of psychiatric disturbance. Archives of General Psychiatry 33:766–771,1976
14.
Salokangas RKR, Honkonen T, Stengård E: Discharged schizophrenia patients in the community: implications for service development: a follow-up study of schizophrenia patients discharged from Finnish mental hospitals in 1982, 1986, 1990, and 1994. Psychiatria Fennica Supplement 2:111–122,2001
15.
Honkonen T, Saarinen S, Salokangas RKR: Deinstitutionalization and schizophrenia in Finland: II. Discharged patients and their psychosocial functioning. Schizophrenia Bulletin 25:547–555,1999
16.
Salokangas RKR, Stengård E, Honkonen T, et al: Sairaalasta yhteiskuntaan: seurantatutkimus sairaalasta kotiuttamisen vaikutuksista skitsofreniapotilaan elämään ja hoitotilanteeseen [From Hospital to Society: A Follow-up Study of the Effects of Discharge From the Hospital on the Life and Treatment Situation of Schizophrenia Patients]. Raportteja [Reports of the National Research and Development Centre for Welfare and Health]:248 Saarijärvi, Stakes,2000
17.
Salokangas RKR, Honkonen T, Stengård E, et al: To be or not to be married—that is the question of quality of life in men with schizophrenia. Social Psychiatry and Psychiatric Epidemiology 36:381–390,2001
18.
Norman RMG, Malla AK, McLean T, et al: The relationship of symptoms and level of functioning in schizophrenia to general wellbeing and the quality of life. Acta Psychiatrica Scandinavica 102:303–309,2000
19.
Salokangas RKR: Prognostic implications of the sex of schizophrenic patients. British Journal of Psychiatry 142:145–151,1983
20.
Wattie BJS, Kedward HB: Gender differences in living conditions found among male and female schizophrenic patients on a follow-up study. International Journal of Social Psychiatry 31:205–216,1985
21.
Alanen YO, Räkköläinen V, Laakso J, et al: Towards Need-Specific Treatment of Schizophrenic Psychoses. Heidelberg, Springer-Verlag, 1986
22.
Seeman MV: Current outcome in schizophrenia: women vs men. Acta Psychiatrica Scandinavica 73:609–617,1986
23.
Angermeyer MC, Goldstein JM, Kuehn L: Gender differences in schizophrenia: rehospitalization and community survival. Psychological Medicine 19:365–382,1989
24.
Salokangas RKR, Stengård E: Gender and short-term outcome in schizophrenia. Schizophrenia Research 3:333–345,1990
25.
Hansson L, Middelboe T, Merinder L, et al: Predictors of subjective quality of life in schizophrenic patients living in the community: a Nordic multicentre study. International Journal of Social Psychiatry 45:247–259,1999
26.
Roder-Wanner UU, Oliver JPJ, Priebe S: Does quality of life differ in schizophrenic women and men? An empirical study. International Journal of Social Psychiatry 43:129–143,1997
27.
Jeste DV, Gladsjo JA, Lindamer LA, et al: Medical comorbidity in schizophrenia. Schizophrenia Bulletin 22:413–430,1996
28.
Stroup TS, Gilmore JH, Jarskog LF: Management of medical illness in persons with schizophrenia. Psychiatric Annals 30:35–40,2000
29.
Stengård E, Honkonen T, Koivisto AM, et al: Satisfaction of caregivers of patients with schizophrenia in Finland. Psychiatric Services 51:1034–1039,2000
30.
McCormack HM, Horne DJ, Sheather S: Clinical applications of visual analogy scales: a critical review. Psychological Medicine 18:1007–1019,1988
31.
Miller RD, Ferris DG: Measurement of subjective phenomena in primary care research: the Visual Analogy Scale. Family Practice Research Journal 13:15–24,1993

Information & Authors

Information

Published In

Go to Psychiatric Services
Go to Psychiatric Services
Psychiatric Services
Pages: 373 - 381
PubMed: 16524996

History

Published online: 1 March 2006
Published in print: March 2006

Authors

Details

Raimo K. R. Salokangas, M.D., Ph.D.
Teija Honkonen, M.D., Ph.D.
Anna-Maija Koivisto, M.Sc.

Metrics & Citations

Metrics

Citations

Export Citations

If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Simply select your manager software from the list below and click Download.

For more information or tips please see 'Downloading to a citation manager' in the Help menu.

Format
Citation style
Style
Copy to clipboard

View Options

View options

PDF/EPUB

View PDF/EPUB

Login options

Already a subscriber? Access your subscription through your login credentials or your institution for full access to this article.

Personal login Institutional Login Open Athens login
Purchase Options

Purchase this article to access the full text.

PPV Articles - Psychiatric Services

PPV Articles - Psychiatric Services

Not a subscriber?

Subscribe Now / Learn More

PsychiatryOnline subscription options offer access to the DSM-5-TR® library, books, journals, CME, and patient resources. This all-in-one virtual library provides psychiatrists and mental health professionals with key resources for diagnosis, treatment, research, and professional development.

Need more help? PsychiatryOnline Customer Service may be reached by emailing [email protected] or by calling 800-368-5777 (in the U.S.) or 703-907-7322 (outside the U.S.).

Media

Figures

Other

Tables

Share

Share

Share article link

Share