The burden on relatives of people with schizophrenia may be influenced not only by patient and caregiver characteristics (Reference BaronetBaronet, 1999; Reference LoukissaLoukissa, 1995), but also by national differences in mental healthcare service provision. However, the results of the two international studies so far available are ambiguous. Magliano et al (Reference Magliano, Fadden and Madianos1998) found greater family burden in Italy, Greece and Portugal and a lesser burden in Germany and Britain; they supposed a divide between Mediterranean and northern European countries. Van Wijngaarden et al (Reference Van Wijngaarden, Schene and Koeter2003) observed a greater burden in Italy and Britain compared with The Netherlands, Spain and Denmark; they proposed that differences in mental health provision might be important. We evaluate this assumption by comparing Germany and Britain, two northern European countries that differ appreciably in the provision of mental health services. We analyse for the first time data from several centres in each country. Data were gathered at five time points, reflecting the situation of relatives over a 2-year time period.
METHOD
Sample
For our analysis of family burden, we chose two northern European countries that differ appreciably in the style of mental health service provision: Germany and Britain. The current per capita expenditure on mental health in Germany is appreciably higher than in Britain (US $289 v. $203) (Statistisches Bundesamt, 1998; World Health Organization, 2005). Germany has on average 7.5 psychiatric beds per 10 000 population, whereas Britain has only 5.8 (World Health Organization, 2005). The differences in the provision of mental health services for people with severe mental illness have been demonstrated using the European Service Mapping Schedule (Reference Becker, Huelsmann and KnudsenBecker et al, 2002; Reference Angermeyer, Roick, Becker and KirchAngermeyer et al, 2004). A comparison between Leipzig and London is particularly revealing: in Leipzig there were 14.7 in-patient beds per 10 000 inhabitants, in London only 6.3. In addition, the provision of services for day and structured activities in Leipzig was greater than in London (71.7 v. 42.6 users per 10 000 inhabitants per working day). However, access to residential care (2.9 v. 4.4 places per 10 000 inhabitants) and to out-patient and community care (99.7 v. 110.5 users per 10 000 inhabitants per month) was somewhat less in Leipzig than in London. Overall, the number of unmet needs for care (covering the dimensions basic living conditions, healthcare, social contact, functioning and services) seems higher among people with schizophrenia in Britain. Patients in London reported on average 2.3 types of unmet needs, those in Leipzig only 1.0 (Reference Kilian, Bernert and MatschingerKilian et al, 2001; Reference McCrone, Leese and ThornicroftMcCrone et al, 2001). The overall satisfaction with mental health services is a proxy indicator of the quality of patients’ treatment, and in patients with schizophrenia from Leipzig it was clearly higher (4.0) than in those from London (3.4) (Reference Mory, Matschinger and RoickMory et al, 2001; Reference Ruggeri, Lasalvia and BisoffiRuggeri et al, 2003). Finally, satisfaction with relatives’ involvement in psychiatric care, which is particularly relevant to family burden, is distinctly lower in Britain than in Germany (London 2.9 v. Leipzig 3.8) (Reference Mory, Matschinger and RoickMory et al, 2001; Reference Ruggeri, Lasalvia and BisoffiRuggeri et al, 2003).
Our analysis is based on the European Schizophrenia Cohort (EuroSC) study carried out between 1998 and 2002 and described elsewhere in more detail (Reference Bebbington, Angermeyer and AzorinBebbington et al, 2005). In the present study we analyse EuroSC data from Germany (n=618) and Britain (n=302). In each of these countries, catchment areas were chosen that were socio-demographically distinct and had different styles of service delivery, in order that between them they should be reasonably representative of the country as a whole.
The study in Germany was based in four catchment areas: the city of Leipzig (490 000 inhabitants) and the county of Altenburg (120 000 inhabitants living in villages and medium-sized towns) in former East Germany, together with the district of Hemer (the cities of Hemer, Iserlohn and Werdohl; 160 000 inhabitants) and the county of Heilbronn (500 000 inhabitants living in villages and medium-sized towns) in former West Germany. In Britain two centres were chosen: Islington, a socially deprived inner-city area of London (176 000 inhabitants), and the reasonably affluent semi-rural area of Leicestershire (330 000 inhabitants).
In each centre, we identified and assessed a cohort of patients aged 18–64 years with a diagnosis of schizophrenia (according to DSM–IV criteria; American Psychiatric Association, 1994) and in contact with secondary psychiatric services. Homeless people, patients in forensic facilities and patients hospitalised for the preceding 12 months were excluded. The psychiatrists treating the patients helped with recruitment. All patients provided informed consent for participation in the study, which was approved by local ethical committees in Germany and the UK.
All recruited patients were asked if we could contact their key relatives, who were defined as the patient's main informal contact person. In 417 cases (Germany n=285, Britain n=132), either the patient or the relative declined or could not participate in the study. Data about non-participants, which were recorded only in Leipzig, show that in 44% of these cases the patient had no key relative, 27% did not permit contact with their key relative, in 25% of cases relatives refused to take part in the study, and in 3% of cases the relatives were unable to take part in the study owing to their own illness or extreme age. Thus, in Germany the response rate was 68% of eligible dyads and it was probably similar in the UK.
In 503 cases (Germany n=333, Britain n=170) patients allowed us to contact their key relatives and the relatives agreed to take part in the study. Patients and caregivers were examined five times at 6-month intervals. We collected data over a total period of 2 years.
Instruments
All relatives were asked to complete the Involvement Evaluation Questionnaire (IEQ; Reference Van Wijngaarden, Schene and KoeterVan Wijngaarden et al, 2000; Reference Bernert, Kilian and MatschingerBernert et al, 2001). This self-administered questionnaire covers a broad domain of caregiving consequences and refers to burden experienced within the past 4 weeks. The instrument contains 27 core variables scored on five-point Likert scales (‘never’ to ‘always’). These variables are summarised in a total score, comprising four distinct sub-scales (Reference Van Wijngaarden, Schene and KoeterVan Wijngaarden et al, 2000):
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(a) ‘Supervision’ (six items), referring to the relatives’ tasks of monitoring the patients’ medicine intake, sleep and dangerous behaviour;
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(b) ‘Worrying’ (six items), covering serious concerns about the patient's health, safety and future;
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(c) ‘Tension’ (nine items), referring to a strained interpersonal atmosphere between patient and relative (this subscale contains one item also used in the sub-scale ‘supervision’ and one also used in the sub-scale ‘worrying’);
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(d) ‘Urging’ (eight items), referring to activation and motivation of the patient, such as encouragement of the patient to undertake activities.
The questionnaire also includes socio-demographic variables, a question regarding the number of hours per week patients and their relatives spend in face-to-face or telephone contact, and an item asking the relatives how well they cope with the patient's mental problems. The response categories of the last item are scored on five-point Likert scales from ‘not at all’ to ‘completely’.
The IEQ was originally developed in The Netherlands. The translation into German and English included an initial translation by professional translators, who were informed about the content of the IEQ; a back-translation into Dutch by a native speaker; a comparison of the back-translation with the original version of IEQ, discussed by the translator and the researchers; and a discussion of the translated questionnaire in focus groups consisting of caregivers and researchers. With this procedure, which is described in more detail elsewhere (Reference Van Wijngaarden, Schene and KoeterVan Wijngaarden et al, 2000; Reference Bernert, Kilian and MatschingerBernert et al, 2001), the translated versions were revised step by step, until they covered domains of family burden in an acceptably similar manner to the original. The validation of the translated versions showed that the IEQ scales had substantial reliability in both countries (Reference Van Wijngaarden, Schene and Koetervan Wijngaarden et al, 2000; Reference Bernert, Kilian and MatschingerBernert et al, 2001).
Patients were examined in face-to-face interviews by psychiatrists and psychologists who were independent of patient care, and who had completed a thorough interviewer training. The diagnosis of schizophrenia was confirmed using the Schedules for Clinical Assessment in Neuropsychiatry (SCAN; Reference Wing, Babor and BrughaWing et al, 1990). Patients were included in the study if their present state or their psychiatric history justified the diagnosis of schizophrenia. The severity of illness was assessed by means of the Positive and Negative Syndrome Scale (PANSS; Kay et al, Reference Kay, Fiszbein and Opler1987, Reference Kay, Opler and Lindenmayer1989) referring to symptoms experienced within the preceding week.
Statistical analysis
The analytical strategy to establish national differences in caregiver burden relied on controlling for the characteristics of relatives and patients that might provide an account of national differences at the individual level. Clearly, if doing this eliminated national differences, this would effectively refute the possibility of an account in terms of national styles of service provision. The analyses relied on chi-squared tests, t-tests, the Mann–Whitney U-test and the Kolmogorov–Smirnov test, as appropriate. Random-effect error component regression models for unbalanced panel data were computed, using robust variance estimators (Reference BaltagiBaltagi, 2001). The IEQ total score and the four IEQ sub-scores provided the dependent variables of the models. In addition to the ‘country’ variable, patient and caregiver characteristics known to predict family burden or differing significantly between the national samples were included in the models as independent variables in order to control their effects. Random-effect error component regression models provide estimations combined for effects of time-invariant differences between participants on the dependent variable and for effects of transitory changes of the independent variables over time. Calculations were carried out using the Statistical Package for the Social Sciences (SPSS) version 11 and Stata version 9.0 for Windows.
RESULTS
Table 1 shows the socio-demographic characteristics of the sample at baseline. The mean age of caregivers was 49 years; almost two-thirds of them were female, and a third were parents of the affected patients. Two-thirds of the relatives were living with the patient. On average, the relatives reported a considerable capacity for coping with the patient's behaviour (mean score 3.7, s.d.=1.1). The two national samples showed no significant difference with regard to the caregivers’ gender, age and marital status, and the proportion who were parents of patients or who lived with them. However, the British sample included a higher proportion of caregivers who were spending less than 9 h weekly with the patient (P=0.008). Furthermore, caregivers from Britain were more pessimistic about their ability to cope with the patient's behaviour than those from Germany (P=0.009).
Characteristics of key relatives and patients
| Germany (n=333) | Britain (n=170) | P | |
|---|---|---|---|
| Key relatives | |||
| Gender, % males | 38 | 35 | 0.576 |
| Age, years: mean (s.d.) | 49 (16) | 51 (14) | 0.097 |
| Marital status, % | |||
| Single | 14 | 22 | |
| Married/living with partner | 76 | 68 | 0.107 |
| Divorced/living apart | 9 | 8 | |
| Widowed | 1 | 2 | |
| Relationship with the patient, % | |||
| Parent | 30 | 36 | 0.164 |
| Other | 70 | 64 | |
| Living with the patient, % | 64 | 69 | 0.346 |
| Time spent with the patient, % | |||
| <9 h/week | 29 | 41 | 0.008 |
| 9-32 h/week | 26 | 15 | |
| >32 h/week | 45 | 43 | |
| Ability to cope with patient's behaviour: mean (s.d.)1 | 3.8 (0.9) | 3.5 (1.4) | 0.009 |
| Patients | |||
| Gender, % male | 55 | 68 | 0.005 |
| Age, years: mean (s.d.) | 39 (10) | 39 (12) | 0.782 |
| Marital status, % | |||
| Single | 48 | 69 | <0.001 |
| Married | 26 | 15 | |
| Living as couple | 9 | 5 | |
| Divorced/living apart | 17 | 9 | |
| Widowed | 0 | 2 | |
| Currently employed, % | 15 | 24 | 0.025 |
| PANSS score: mean (s.d.) | 54.0 (19.1) | 46.0 (14.4) | <0.001 |
| Negative symptom score | 14.9 (7.0) | 11.9 (6.1) | <0.001 |
| Positive symptom score | 11.2 (4.9) | 10.5 (4.8) | 0.019 |
| Duration of illness, years: mean (s.d.) | 13 (9) | 13 (10) | 0.817 |
The patient sample had a mean age of 39 years, and patients had been mentally ill on average for 13 years (Table 1), with no difference between the samples from German and Britain. However, patients from Britain included fewer married people (P<0.001), but more men (P=0.005) and more currently employed people (P=0.025). Additionally, patients from Britain had lower PANSS positive (P=0.019) and negative (P<0.001) symptom scores. The differences between the samples from Britain and Germany are also seen in variables known to be predictors of family burden; thus, a valid analysis of national differences in family burden must include controlling for the influence of these variables. For this reason the absolute values of the family burden have limited meaning; we nevertheless present them for the sake of completeness.
The total mean IEQ burden score of caregivers was 43.2 (s.d.=13.0) in Germany and 46.1 (s.d.=16.8; P=0.087) in Britain. The four IEQ sub-scales showed that in both countries the greatest caregiver burden resulted from worries about the patient, and the least from supervisory obligations. There was no significant difference between Germany and Britain in burden from supervision, worrying or tension, but caregivers from Britain had significantly higher scores on the ‘urging’ components of the IEQ (P<0.001).
Table 2 shows the regression model with the IEQ total score as the dependent variable. Independently of national location, burden was associated with caregiver variables: being the patient's parent, spending more hours with the patient and having less capacity to cope with the patient's behaviour. Of the patients’ characteristics, high PANSS positive and negative symptom scores were linked to an increase in caregivers’ burden, along with male gender, current unemployment and being married. However, the model indicates that, after controlling for individual level variables, ‘country’ remains a significant predictor of caregiver burden (P=0.027), caregivers from Britain being more burdened than those from Germany. The model explained 22% of the variance in caregivers’ burden.
Regression model with Involvement Evaluation Questionnaire total score as dependent variable (number of groups 419, average observations per group 2.4)
| Independent variables | Coeff. | s.e. robust | P |
|---|---|---|---|
| Country (0 Britain, 1 Germany) | -3.412 | 1.545 | 0.027 |
| Caregivers’ gender (0 male, 1 female) | 0.712 | 1.258 | 0.571 |
| Caregivers’ relationship with patient (0 not parent, 1 parent) | 3.154 | 1.269 | 0.013 |
| Caregivers’ weekly hours spent with patient | 0.560 | 0.257 | 0.030 |
| Caregivers’ ability to cope with patient's behaviour | -2.091 | 0.430 | <0.001 |
| Patients’ PANSS score | |||
| Positive symptoms | 0.583 | 0.112 | <0.001 |
| Negative symptoms | 0.254 | 0.074 | 0.001 |
| Patients’ gender (0 male, 1 female) | -4.210 | 1.299 | 0.001 |
| Patients’ working situation (0 not employed, 1 employed) | -4.971 | 1.408 | <0.001 |
| Patients’ marital status (0 not married, 1 married) | 4.579 | 1.667 | 0.006 |
| Constant | 50.223 | 2.330 | <0.001 |
| R 2 overall | 0.22 |
Table 3 shows predictors of the family burden sub-scales. Although the burden was higher in Britain for all sub-scales, it was only significantly so for the sub-scale ‘urging’ (that is, the encouragement of motivation and activity) (P<0.001). In contrast, patient's positive symptom scores, as well as caregivers’ ability to cope and the patient's marital status, predicted family burden in all four IEQ sub-scales. In each sub-scale, higher caregiver burden was found in relatives of married patients, in caregivers with lower coping abilities and in caregivers of patients with higher positive symptom scores. Higher negative symptom scores were also significantly associated with greater family burden reported in the sub-scales ‘urging’, ‘worrying’, and ‘supervision’ but not ‘tension’. Caregivers in greater contact with the patients experienced more burden related to ‘urging’. Additionally, the parents of patients had higher scores on the ‘worrying’ sub-scale. Relatives of male patients had greater burden in the domains ‘urging’, ‘tension’ and ‘supervision’. In contrast, relatives of currently employed patients experienced less burden in the domains ‘urging’, ‘supervision’ and ‘worrying’. The independent variables mentioned above explain 14–23% of the variance in the burden indicated by the IEQ sub-scales.
Regression models with Involvement Evaluation Questionnaire sub-scale scores as dependent variables
| Independent variables | Urging (coeff.) | Tension (coeff.) | Supervision (coeff.) | Worrying (coeff.) |
|---|---|---|---|---|
| Country (0 Britain, 1 Germany) | -2.629*** | -0.658 | -0.198 | -0.500 |
| Caregivers’ gender (0 male, 1 female) | 0.265 | 0.607 | 0.260 | 0.514 |
| Caregivers’ relationship with patient (0 not parent, 1 parent) | 0.461 | 0.341 | 0.277 | 2.459*** |
| Caregivers’ weekly hours spent with patient | 0.372*** | 0.129 | 0.106 | 0.071 |
| Caregivers’ ability to cope with patient's behaviour | -0.436* | -0.917*** | -0.308** | -0.789*** |
| Patients’ PANSS score | ||||
| Positive symptoms | 0.126** | 0.160*** | 0.095*** | 0.258*** |
| Negative symptoms | 0.132*** | 0.033 | 0.033* | 0.078** |
| Patients’ gender (0 male, 1 female) | -1.629** | -0.863* | -1.319*** | -0.561 |
| Patients’ working situation (0 not employed, 1 employed) | -1.967*** | -0.534 | -0.944** | -1.859*** |
| Patients’ marital status (0 not married, 1 married) | 1.449* | 1.731** | 0.835* | 1.278* |
| Constant | 15.369*** | 15.459*** | 9.117*** | 13.850*** |
| R 2 overall | 0.19 | 0.17 | 0.14 | 0.23 |
DISCUSSION
The total burden reported by the caregivers in our sample corresponds well with results from other studies. Thus, Van Wijngaarden et al (Reference Van Wijngaarden, Schene and Koeter2000) found a mean total IEQ score of 50.6 in their pooled sample from five European countries. As in our investigation, those authors showed that relatives of people with schizophrenia experience the highest burden from worries and the lowest burden in relation to the supervision of the patient.
Our investigation clearly showed that caregiver burden in Britain is greater than in Germany, despite less time in mutual contact, less psychopathology and a better employment situation in the patient sample. Because our analysis controlled for significant patient and caregiver characteristics, the national difference in family burden may in part be explained by differences in the mental healthcare system. One reason could be that Germany has considerably more psychiatric beds than Britain. In Britain the main focus of mental healthcare is thus more in the extramural domain. Even in times of acute illness, this would tend to increase contact between patient and relative, with a consequent increase in burden. The fact that it did not might indicate an active process of withdrawal, which was nevertheless ineffective. Van Wijngaarden et al (Reference Van Wijngaarden, Schene and Koeter2003) in their study on family burden in five European countries indeed found that IEQ levels tended to be higher where the number of psychiatric beds per capita was lower.
Furthermore, opportunities for daytime structured activities (which include work and work-related activities as well as other structured activities and social contact) are better in Germany than in Britain (Reference Becker, Huelsmann and KnudsenBecker et al, 2002; Reference Angermeyer, Roick, Becker and KirchAngermeyer et al, 2004). This could also affect caregivers’ burden. Thus, Stengard et al (Reference Stengard, Honkonen and Koivisto2000) argue that a link exists between patients’ use of rehabilitative services and the burden on their caregivers. However, the higher proportion of working patients in the British sample might indicate that vocational services are better in Britain than in Germany. Although the proportions of sheltered or voluntarily employed participants were similar in both samples (7.5% in Germany, 4.7% in Britain), the proportion of paid or self-employed participants was higher in the British sample (7.8% in Germany, 18.8% in Britain). Although this might be the result of more successful vocational services, the lower severity of illness in the British sample and the better labour market situation in Britain probably had the greater influence – in 2005 the unemployment rate in Germany was 9.5% whereas in Britain it was only 4.7% (Statistical Office of the European Communities, 2006).
Although Germany provides more inpatient care (233% of the capacity in Britain) and more day and structured activities (168% of the capacity in Britain), it has less residential care (66% of the capacity in Britain) and less out-patient and community care (90% of the capacity in Britain) (Reference Angermeyer, Roick, Becker and KirchAngermeyer et al, 2004). Consequently, Britain has at least in some service areas a better mental healthcare system than Germany. This might counter the assumption that the observed differences in family burden are caused by differences in mental healthcare provision. However, the differences in residential and out-patient or community care are small compared with those in in-patient care and day and structured activities. Moreover, the better opportunities for out-patient and community care once again support the assertion that in Britain the main focus of mental healthcare is in the extramural domain, which might in practice be connected with increased family burden. In contrast, the better opportunities for residential care should in principle actually decrease family burden (Reference Tessler and GamacheTessler & Gamache, 1994); in our study, however, they probably did not have an important influence, because the utilisation of these services scarcely differed between the two samples (British sample 6.5%, German sample 7.2%; P=0.631).
However, family burden might be influenced not only by the quantity of mental health service provision, but also by its accessibility and quality. There is some evidence relating to this. Thus, the higher number of unmet needs for care observed in patients from Britain with schizophrenia (Reference Kilian, Bernert and MatschingerKilian et al, 2001; Reference McCrone, Leese and ThornicroftMcCrone et al, 2001) might contribute to a greater burden on caregivers. Meijer et al (Reference Meijer, Schene and Koeter2004) reported such an association, especially for the IEQ domains ‘worrying’ and ‘urging’. In our sample the greatest differences between relatives from Britain and Germany were also in the IEQ sub-scale ‘urging’. This suggests that insufficient support for patients in Britain requires relatives to take over, entirely or partly, tasks that are covered by the mental healthcare system in Germany. Such tasks include urging patients to take proper care of themselves or to undertake some kind of activity, accompanying them to outside venues, and ensuring that they have taken the required medicine. If such tasks are undertaken by professional staff in day and structured activity services, the caregivers are consequently relieved of them.
In addition to national differences, our study confirmed patient and caregiver characteristics already known to be associated with family burden. Thus, reduced family burden was predicted by better caregiver coping abilities (Reference Budd, Oles and HughesBudd et al, 1998; Reference Magliano, Fadden and MadianosMagliano et al, 1998; Reference BaronetBaronet, 1999), and less severe positive and negative symptoms in the patient (Reference Provencher and MueserProvencher & Mueser, 1997; Reference Schene, van Wijngaarden and KoeterSchene et al, 1998; Reference Wolthaus, Dingemans and ScheneWolthaus et al, 2002; Reference Lowyck, De Hert and PeetersLowyck et al, 2004). This applied not only to the IEQ total score, but also to all four sub-scales of burden. Our results also confirm that caregivers in greater contact with the patient experience greater burden (Reference Winefield and HarveyWinefield & Harvey, 1994; Reference Schene, van Wijngaarden and KoeterSchene et al, 1998; Reference WarnerWarner, 2000). This was especially the case with regard to patient activation and motivation tasks (sub-scale ‘urging’). Additionally, our study indicates that parents may be more burdened than other relatives, as was also found by Lowyck et al (Reference Lowyck, De Hert and Peeters2004). Not unexpectedly, caregiving parents seem especially prone to high levels of worry over their ill children.
Our results are also in line with those of Hoenig & Hamilton (Reference Hoenig and Hamilton1966), who found that relatives of male patients reported more subjective and objective burden than those of female patients. Pickett et al (Reference Pickett, Greenley and Greenberg1995) showed that the burden experienced by family members, especially their worries, was less when the ill person was employed. Again, we found the same. To our knowledge no one has previously documented the high levels of burden experienced by the family members of married patients. This connection only applies to those who are married, not cohabiting. This may reflect the fact that, for the most part, these patients married before they fell ill. Their spouses may consequently sense a heavier burden on their life and on their future plans than partners who got to know the patient after the illness began.
Limitations
The aim of our investigation was to examine whether national differences between Germany and Britain in the burden experienced by the caregivers of people with schizophrenia could be explained solely in terms of individual attributes, or whether some of the differences might derive from attributes of the healthcare system. We did this by controlling for patient and caregiver characteristics known to predict family burden or differing significantly between the samples. However, although the level of social support received by relatives is a known predictor of care-related burden (Reference Magliano, Fadden and MadianosMagliano et al, 1998), we had no information about this and therefore could not control for it.
Although our results reflect the situation in the catchment areas chosen, they may be generalisable to the situation in the countries as a whole, given that the catchment areas were chosen to be jointly representative (Reference Bebbington, Angermeyer and AzorinBebbington et al, 2005). However, it has been taken into account that the German study population did not contain a sample from a major, multicultural city equivalent to London, with its inner-city catchment area of Islington. Therefore, the British sample might have included more individuals with multiple psychosocial problems, which may explain some of the variance observed in the study. Furthermore, we had no comparable data about the amount of caregiver service provision in Germany and Britain, although the amount of professional support to relatives may be related to the burden experienced (Reference WarnerWarner, 2000).
Finally, we were unable to provide a true non-response rate among eligible dyads in Britain. Given the similarity of the non-participation rates, the British non-response rate was probably also similar to that in Germany, where it was an acceptable 68%.
Concluding remarks
Differences in the caregiving burden reported by relatives of people with schizophrenia in Britain and Germany persisted even after we controlled for patient and caregiver characteristics. These differences may well be related to the different healthcare systems in the two countries. Our results suggest that, in comparison with Germany, the support of patients with schizophrenia falls more to the informal than the professional healthcare domains in Britain. This possibility should be analysed more closely in future studies, in particular whether the cost savings achieved at the expense of relatives ultimately result in health problems from the increased care-related burden. Family burden is of course only one aspect of mental healthcare. Patient outcomes are the other important aspect that must be more intensively addressed in future international health system comparisons.
Acknowledgements
The study was funded by H. Lundbeck A/S and by grants from the German Federal Ministry of Education and Research in the framework of the Research Association Public Health Saxony (grant 01EG9732/7).
The EuroSC Research Group is composed of the following: Altenburg: I. Lindenbach, M. Swiridoff; Eppingen: F. Baehr, G. Lauer, T. Schwarz; Hemer: V. Becker, J. Höffler, K. Siegrist, U. Trenckmann; Leicester: T. Brugha, J. Smith, D. Bagchi, S. McCormack, S. Wheatley; Leipzig: M. Angermeyer, S. Bernert, R. Kilian, H. Matschinger, C. Mory, C. Roick; Lille: M. Goudemand, D. Beaune, S. Dumont; London: P. Bebbington, D. Ellis, L. Isham, S. Johnson, J. Pearson, E. Perez, A. Regan, R. White; Lyon: B. Lachaux, P. Pasi-Delay, S. Declerck; Marseille: J. M. Azorin, J. P. Chabannes, P. Chiaroni, I. Banovic; Lundbeck A/S: M. Toumi, Å. Kornfeld, K. Hansen, C. Morin, L. Munier, J. C. Nachef, C. Nickel, C. Sapin, V. Willacy.
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