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Socio-demographic, clinical characteristics and utilization of mental health care services associated with SF-6D utility scores in patients with mental disorders: contributions of the quantile regression

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Abstract

Purpose

Health-related quality of life (HRQoL) is a widely used concept in the assessment of health care. Some generic HRQoL instruments, based on specific algorithms, can generate utility scores which reflect the preferences of the general population for the different health states described by the instrument. This study aimed to investigate the relationships between utility scores and potentially associated factors in patients with mental disorders followed in inpatient and/or outpatient care settings using two statistical methods.

Methods

Patients were recruited in four psychiatric sectors in France. Patient responses to the SF-36 generic HRQoL instrument were used to calculate SF-6D utility scores. The relationships between utility scores and patient socio-demographic, clinical characteristics, and mental health care utilization, considered as potentially associated factors, were studied using OLS and quantile regressions.

Results

One hundred and seventy six patients were included. Women, severely ill patients and those hospitalized full-time tended to report lower utility scores, whereas psychotic disorders (as opposed to mood disorders) and part-time care were associated with higher scores. The quantile regression highlighted that the size of the associations between the utility scores and some patient characteristics varied along with the utility score distribution, and provided more accurate estimated values than OLS regression.

Conclusions

The quantile regression may constitute a relevant complement for the analysis of factors associated with utility scores. For policy decision-making, the association of full-time hospitalization with lower utility scores while part-time care was associated with higher scores supports the further development of alternatives to full-time hospitalizations.

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References

  1. Sorenson, C., Drummond, M., & Kanavos, P. (2008). Ensuring value for money in health care, the role of health technology assessment in the European Union. Copenhagen: European Observatory on Health Systems and Policies.

    Google Scholar 

  2. Drummond, M. F., O’Brien, B., Stoddart, G. L., & Torrance, G. W. (1997). Methods for the economic evaluation of health care programmes (2nd ed.). New York: Oxford University Press.

    Google Scholar 

  3. Mavranezouli, I. (2010). A review and critique of studies reporting utility values for schizophrenia-related health states. Pharmacoeconomics, 28(12), 1109–1121.

    Article  PubMed  Google Scholar 

  4. Feeny, D. (2000). A utility approach to the assessment of health-related quality of life. Medical Care, 38(9, sup 2), 151–154.

    Google Scholar 

  5. World Health Organization (WHO). (2001). The world health report: 2001: Mental health: New understanding, new hope. Geneva: WHO.

    Google Scholar 

  6. Mack, S., Jacobi, F., Beesdo-Baum, K., Gerschler, A., Strehle, J., Höfler, M., et al. (2015). Functional disability and quality of life decrements in mental disorders: Results from the mental health module of the German health interview and examination survey for adults (DEGS1-MH). European Psychiatry, 30, 793–800.

    Article  PubMed  Google Scholar 

  7. Caron, J., Mercier, C., Diaz, P., & Martin, A. (2005). Socio-demographic and clinical predictors of quality of life in patients with schizophrenia or schizo-affective disorder. Psychiatry Research, 137, 203–213.

    Article  PubMed  Google Scholar 

  8. Fleury, M. J., Grenier, G., Bamvita, J. M., Tremblay, J., Schmitz, N., & Caron, J. (2013). Predictors of quality of life in a longitudinal study of users with severe mental disorders. Health and Quality of Life Outcomes. doi:10.1186/1477-7525-11-92.

    PubMed  PubMed Central  Google Scholar 

  9. Lokkerbol, J., Adema, D., de Graaf, R., ten Have, M., Cuijpers, P., Beekman, A., et al. (2013). Non-fatal burden of disease due to mental disorders in the Netherlands. Social Psychiatry and Psychiatric Epidemiology, 48, 1591–1599.

    Article  PubMed  Google Scholar 

  10. Ruggieri, M., Gater, R., Barbui, C., & Tansella, M. (2002). Determinants of subjective quality of life in patients attending community-based mental health services. The South-Verona Outcome Project 5. Acta Psychiatrica Scandinavica, 105, 131–140.

    Article  Google Scholar 

  11. Mercier, C., Péladeau, N., & Tempier, R. (1998). Age, gender and quality of life. Community Mental Health Journal, 34, 487–500.

    Article  CAS  PubMed  Google Scholar 

  12. Eklund, M., Hansson, L., & Bejerholm, U. (2001). Relationships between satisfaction with occupational factors and health-related variables in schizophrenia outpatients. Social Psychiatry and Psychiatric Epidemiology, 36, 79–85.

    Article  CAS  PubMed  Google Scholar 

  13. Nordt, C., Müller, B., Rössler, W., & Lauber, C. (2007). Predictors and course of vocational status, income, and quality of life in people with severe mental illness: A naturalistic study. Social Science and Medicine, 65, 1420–1429.

    Article  PubMed  Google Scholar 

  14. Caron, J., Tempier, R., Mercier, C., & Leouffre, P. (1998). Components of social support and quality of life in severely mentally ill, low income individuals and a general population group. Community Mental Health Journal, 34(5), 459–475.

    Article  CAS  PubMed  Google Scholar 

  15. Saarni, S. I., Suvisaari, J., Sintonen, H., Pirkola, S., Koskinen, S., Aromaa, A., et al. (2007). Impact of psychiatric disorders on health-related quality of life: General population survey. The British Journal of Psychiatry, 190, 326–332.

    Article  PubMed  Google Scholar 

  16. Fernández, A., Bellón Saameño, J. Á., Pinto-Meza, A., Luciano, J. V., Autonell, J., Palao, D., et al. (2010). Burden of chronic physical conditions and mental disorders in primary care. The British Journal of Psychiatry, 196, 302–309.

    Article  PubMed  Google Scholar 

  17. World Health Organization (WHO). (2005). Mental health: Facing the challenges, building solutions, Report from the WHO European Ministerial Conference. Copenhagen: WHO.

    Google Scholar 

  18. Collins, P. Y., Insel, T. R., Chockalingam, A., Daar, A., & Maddox, Y. T. (2013). Grand challenges in global mental health: Integration in research, policy, and practice. PLoS Medicine. doi:10.1371/journal.pmed.1001434.

    Google Scholar 

  19. Brazier, J. E., Yang, Y., Tsuchiya, A., & Rowen, D. L. (2010). A review of studies mapping (or cross walking) non-preference based measures of health to generic preference-based measures. European Journal of Health Economics, 11, 215–225.

    Article  PubMed  Google Scholar 

  20. Hernández Alava, M., Wailoo, A. J., & Ara, R. (2010). Tails from the peak district: Adjusted censored mixture models of EQ-5D health state utility values. HEDS Discussion Paper 10/08. Sheffiled: School of Health and Related Research.

  21. Browne, C., Brazier, J., Carlton, J., Alavi, Y., & Jofre-Bonet, M. (2012). Estimating quality adjusted life years from patient reported visual functioning. Eye, 26, 1295–1301.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Ara, R., & Brazier, J. (2011). Estimating health state utility values for comorbid health conditions using SF-6D data. Value in Health, 14, 740–745.

    Article  PubMed  Google Scholar 

  23. Räsänen, P., Roine, E., Sintonen, H., Semberg-Konttinen, V., Ryynänen, O. P., & Roine, R. (2006). Use of quality-adjusted life years for the estimation of effectiveness of health care: A systematic literature review. International Journal of Technology Assessment in Health Care, 22(2), 235–241.

    Article  PubMed  Google Scholar 

  24. Koenker, R., & Hallock, K. (2001). Quantile regression. The Journal of Economic Perspectives, 15(4), 143–156.

    Article  Google Scholar 

  25. Prigent, A., Auraaen, A., Kamendje-Tchokobou, B., Durand-Zaleski, I., & Chevreul, K. (2014). Health-related quality of life and utility scores in people with mental disorders: A comparison with the non-mentally ill general population. International Journal of Environmental Research and Public Health, 11, 2804–2817.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Leplège, A., Ecosse, E., Coste, J., Pouchot, J., & Perneger, T. (2001). Le questionnaire MOS SF-36, manuel de l’utilisateur et guide d’interprétation des scores. Paris: Editions Estem.

    Google Scholar 

  27. Brazier, J., Roberts, J., & Deverill, M. (2002). The estimation of a preference-based measure of health from the SF-36. Journal of Health Economics, 21, 271–292.

    Article  PubMed  Google Scholar 

  28. Walters, S. J., & Brazier, J. E. (2005). Comparison of the minimally important difference for two health state utility measures: EQ-5D and SF-6D. Quality of Life Research, 14, 1523–1532.

    Article  PubMed  Google Scholar 

  29. Krieger, N. (1992). Overcoming the absence of socioeconomic data in medical records: Validation and application of a census-based methodology. American Journal of Public Health, 82(5), 703–710.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Diez Roux, A. V., Kiefe, C. I., Jacobs, D. R., Haan, M., Jackson, S. A., et al. (2001). Area characteristics and individual-level socioeconomic position indicators in three population-based epidemiologic studies. Annals of Epidemiology, 11, 395–405.

    Article  CAS  PubMed  Google Scholar 

  31. Morris, R., & Carstairs, V. (1991). Which deprivation? A comparison of selected deprivation indexes. Journal of Public Health Medicine, 13(4), 318–326.

    CAS  PubMed  Google Scholar 

  32. Rey, G., Jougla, E., Fouillet, A., & Hémon, D. (2009). Ecological association between a deprivation index and mortality in France over the period 1997–2001: Variations with special scale, degree of urbanicity, age, gender and cause of death. BMC Public Health, 9, 33.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Guy, W., (Ed.). (1976). ECDEU assessment manual for psychopharmacology. Rockville, MD: Department of Health, Education, and Welfare.

  34. Seymour, J., McNamee, P., Scott, A., & Tinelli, M. (2010). Shedding new light onto the ceiling and floor? A quantile regression approach to compare EQ-5D and SF-6D responses. Health Economics, 19(6), 683–696.

    PubMed  Google Scholar 

  35. Tinelli, M., Ryan, M., Bond, C., & Scott, A. (2013). Valuing benefits to inform a clinical trial in pharmacy. Do differences in utility measures at baseline affect the effectiveness of the intervention? PharmacoEconomics, 31, 163–171.

    Article  PubMed  Google Scholar 

  36. Koenker, R. (1994). Confidence intervals for regression quantiles. In Proceedings of the Fifth Prague Symposium on Asymptotic Statistics. New York: Springer.

  37. Koenker, R., & Machado, J. A. F. (1999). Goodness of fit and related inference processes for quantile regression. Journal of the American Statistical Association, 94, 1296–1310.

    Article  Google Scholar 

  38. Longworth, L., & Rowan, D. (2011). NICE DSU technical support document 10: The use of mapping methods to estimate health state utility values. Sheffield: NICE DSU. Retrieved May 25, 2014 from http://www.nicedsu.org.uk.

  39. Bengtsson-Tops, A., Hansson, L., Sandlund, M., Bjarnason, O., Korkeila, J., Merinder, L., et al. (2005). Subjective versus interviewer assessment of global quality of life among persons with schizophrenia living in the community: A Nordic multicenter study. Quality of Life Research, 14, 221–229.

    Article  PubMed  Google Scholar 

  40. Fleury, M. J., Grenier, G., & Bamvita, J. M. (2015). Predictive typology of subjective quality of life among participants with severe mental disorders after a five-year follow-up: A longitudinal two-step cluster analysis. Health and Quality of Life Outcomes. doi:10.1186/s12955-015-0346-x.

    PubMed  PubMed Central  Google Scholar 

  41. Picard, R. R., & Berk, K. N. (1990). Data splitting. The American Statistician, 44(2), 140–147.

    Google Scholar 

  42. Staring, A. B. P., Mulder, C. L., Duivenvoorden, H. J., De Haan, L., & Van der Gaag, M. (2009). Fewer symptoms vs. more side-effects in schizophrenia? Opposing pathways between antipsychotic medication compliance and quality of life. Schizophrenia Research, 113, 27–33.

    Article  CAS  PubMed  Google Scholar 

  43. Bras, H., Liefbroer, A. C., & Elzinga, C. H. (2010). Standardization of pathways to adulthood? An analysis of Dutch cohorts born between 1850 and 1900. Demography, 47(4), 1013–1034.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Elzinga, C. H. (2005). Combinatorial representations of token sequences. Journal of Classification, 22(1), 87–118.

    Article  Google Scholar 

  45. Thornicroft, G., & Tansella, M. (2004). Components of a modern mental health service: A pragmatic balance of community and hospital care, overview of systematic evidence. The British Journal of Psychiatry, 185, 283–290.

    Article  PubMed  Google Scholar 

  46. Ministère du travail, de l’emploi et de la santé, Ministère des solidarités et de la cohésion sociale. (2012). Plan Psychiatrie et Santé Mentale 20112015. Paris: Ministère du travail, de l’emploi et de la santé, Ministère des solidarités et de la cohésion sociale.

  47. Ministère du travail, de l’emploi et de la santé, Ministère des solidarités et de la cohésion sociale. (2005). Plan Psychiatrie et Santé Mentale 20052008. Paris: Ministère du travail, de l’emploi et de la santé, Ministère des solidarités et de la cohésion sociale.

  48. Cour des comptes. (2011). L’organisation des soins psychiatriques: les effets du plan « psychiatrie et santé mentale » (2005–2010). Paris: Cour des comptes.

    Google Scholar 

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Acknowledgements

The authors are indebted to the Daumézon hospital (Centre Hospitalier Départemental Georges Daumézon) staff, in particular the heads of the care services G01, G02, G05, G08, and of the department of medical information as well as their teams, for its collaboration and support for the implementation of the survey. The authors also thank Anaïs Le Jeannic, Marie-Amélie Vinet, and Thomas Lefevre for their participation in the data collection, Sandrine Simon for her support for the design of the survey questionnaire as well as Karen Berg Brigham for her valuable comments on the manuscript.

Funding

This research was undertaken with the support of the FondaMental Foundation, a foundation of scientific cooperation, as well as with the joint support of the French Ministry of Health, General Directorate of Health (Direction Générale de la Santé) and Directorate of Research, Studies, Evaluation and Statistics (Direction de la Recherche, des Etudes, de l’Evaluation et des Statistiques); the general scheme of the statutory health insurance system (Caisse Nationale d’Assurance Maladies des Travailleurs Salariés); the scheme for self-employed people (Régime Social des Indépendants); the National Solidarity Fund for Autonomy (Caisse Nationale de Solidarité pour l’Autonomie) and the National Institute for Prevention and Health Education (Insitut National de Prévention et d’Education pour la Santé) in the context of IReSP’s 2010 call for research projects.

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Correspondence to Amélie Prigent PhD.

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Conflict of interest

Amélie Prigent received a grant from the FondaMental foundation to perform this work. Other authors declare that they have no conflict of interest.

Ethical approval

Ethical approvals for this study were obtained from the French advisory committee on data processing in the health domain research (comité consultatif sur le traitement de l’information en matière de recherche dans le domaine de la santé (CCTIRS), the French national committee of data processing and freedom (commission nationale de l’informatique et des libertés (CNIL)), and the ethical research committee (comité de protection des personnes (CPP)) Ile-de-France IX.

Informed consent

As this study was a non-interventional study, written informed consent was not required. However, each included patient has been informed of the study’s objectives and of the types of data collected (verbally and through a letter of information). Only patients who agreed to participate in the study were included after their non-opposition to participate was orally collected.

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Prigent, A., Kamendje-Tchokobou, B. & Chevreul, K. Socio-demographic, clinical characteristics and utilization of mental health care services associated with SF-6D utility scores in patients with mental disorders: contributions of the quantile regression . Qual Life Res 26, 3035–3048 (2017). https://doi.org/10.1007/s11136-017-1623-4

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