Skip to main content
Top
Published in: Quality of Life Research 5/2012

Open Access 01-06-2012

Assessing health-related quality-of-life changes in informal caregivers: an evaluation in parents of children with major congenital anomalies

Authors: Marten J. Poley, Werner B. F. Brouwer, N. Job A. van Exel, Dick Tibboel

Published in: Quality of Life Research | Issue 5/2012

Login to get access

Abstract

Purpose

Relatively few attempts to measure the effects on the health-related quality of life (HRQoL) of informal caregivers within the context of economic evaluations have been reported. This paper is an exploratory attempt to find suitable methods to assess caregivers’ HRQoL, using a population of parents of children with major congenital anomalies.

Methods

A total of 306 parents of children born with either congenital anorectal malformations (ARM) or congenital diaphragmatic hernia were surveyed. They rated their current HRQoL on the EQ-VAS. After that, they rated their HRQoL again on the assumption that someone would take over their caregiving activities completely and free of charge. Finally, the parents classified their HRQoL on the EQ-5D. The caregivers’ scores on the EQ-VAS and the EQ-5D were compared with scores elicited in the general population.

Results

Most parents indicated that their HRQoL would not change if someone else took on their caregiving activities. Some methodological issues may have influenced this outcome, such as difficulties in self-assessing HRQoL changes due to caregiving, process utility, protest answers, and difficulties in understanding the hypothetical question. The HRQoL of the parents was relatively low compared with population statistics, especially in the parents of children with ARM and in mothers. This can be illustrated by the difference between the mean EQ-5D score of the mothers aged 25–34 years of the children with ARM and that of the general population (0.83 vs. 0.93; P = 0.002).

Conclusions

Significant HRQoL differences exist between parents caring for children with congenital anomalies and the general population. It would be useful to further improve our understanding of the HRQoL impact of informal caregiving, separating ‘caregiving effects’ from ‘family effects’, and distinguishing parent–child relationships from other caregiving situations. This study underlines the importance of considering caregivers, also in the context of economic evaluations. It indicates that general HRQoL measures, as used in patients, may be able to detect HRQoL effects in caregivers, which facilitates the incorporation in common economic evaluations of HRQoL effects in carers. Analysts and policy makers should be aware that if HRQoL improvement is an important aim, they should register HRQoL changes not only in patients but also in their caregivers.
Literature
1.
go back to reference Drummond, M. F., Sculpher, M. J., Torrance, G. W., O’Brien, B. J., & Stoddart, G. L. (2005). Methods for the economic evaluation of health care programmes (3rd ed.). New York: Oxford University Press. Drummond, M. F., Sculpher, M. J., Torrance, G. W., O’Brien, B. J., & Stoddart, G. L. (2005). Methods for the economic evaluation of health care programmes (3rd ed.). New York: Oxford University Press.
2.
go back to reference Gold, M. R., Siegel, J. E., Russell, L. B., & Weinstein, M. C. (Eds.). (1996). Cost-effectiveness in health and medicine. New York: Oxford University Press. Gold, M. R., Siegel, J. E., Russell, L. B., & Weinstein, M. C. (Eds.). (1996). Cost-effectiveness in health and medicine. New York: Oxford University Press.
3.
go back to reference Brouwer, W. B. F., van Exel, N. J. A., Koopmanschap, M. A., & Rutten, F. F. H. (1999). The valuation of informal care in economic appraisal. A consideration of individual choice and societal costs of time. International Journal of Technology Assessment in Health Care, 15(1), 147–160.PubMedCrossRef Brouwer, W. B. F., van Exel, N. J. A., Koopmanschap, M. A., & Rutten, F. F. H. (1999). The valuation of informal care in economic appraisal. A consideration of individual choice and societal costs of time. International Journal of Technology Assessment in Health Care, 15(1), 147–160.PubMedCrossRef
4.
go back to reference National Institute for Health and Clinical Excellence. (2006). Donepezil, galantamine, rivastigmine and memantine for the treatment of Alzheimer’s disease. NICE technology appraisal guidance 111 (amended September 2007). London: National Institute for Health and Clinical Excellence. National Institute for Health and Clinical Excellence. (2006). Donepezil, galantamine, rivastigmine and memantine for the treatment of Alzheimer’s disease. NICE technology appraisal guidance 111 (amended September 2007). London: National Institute for Health and Clinical Excellence.
5.
go back to reference van den Berg, B., Brouwer, W. B. F., & Koopmanschap, M. A. (2004). Economic valuation of informal care. An overview of methods and applications. The European Journal of Health Economics, 5(1), 36–45.PubMedCrossRef van den Berg, B., Brouwer, W. B. F., & Koopmanschap, M. A. (2004). Economic valuation of informal care. An overview of methods and applications. The European Journal of Health Economics, 5(1), 36–45.PubMedCrossRef
6.
go back to reference Koopmanschap, M. A., van Exel, N. J. A., van den Berg, B., & Brouwer, W. B. F. (2008). An overview of methods and applications to value informal care in economic evaluations of healthcare. PharmacoEconomics, 26(4), 269–280.PubMedCrossRef Koopmanschap, M. A., van Exel, N. J. A., van den Berg, B., & Brouwer, W. B. F. (2008). An overview of methods and applications to value informal care in economic evaluations of healthcare. PharmacoEconomics, 26(4), 269–280.PubMedCrossRef
7.
go back to reference Basu, A., & Meltzer, D. (2005). Implications of spillover effects within the family for medical cost-effectiveness analysis. Journal of Health Economics, 24(4), 751–773.PubMedCrossRef Basu, A., & Meltzer, D. (2005). Implications of spillover effects within the family for medical cost-effectiveness analysis. Journal of Health Economics, 24(4), 751–773.PubMedCrossRef
8.
go back to reference Bobinac, A., van Exel, N. J. A., Rutten, F. F. H., & Brouwer, W. B. F. (2010). Caring for and caring about: disentangling the caregiver effect and the family effect. Journal of Health Economics, 29(4), 549–556.PubMedCrossRef Bobinac, A., van Exel, N. J. A., Rutten, F. F. H., & Brouwer, W. B. F. (2010). Caring for and caring about: disentangling the caregiver effect and the family effect. Journal of Health Economics, 29(4), 549–556.PubMedCrossRef
9.
go back to reference Bobinac, A., van Exel, N. J. A., Rutten, F. F. H., & Brouwer, W. B. F. (2011). Health effects in significant others: Separating family and care-giving effects. Medical Decision Making, 31(2), 292–298.PubMedCrossRef Bobinac, A., van Exel, N. J. A., Rutten, F. F. H., & Brouwer, W. B. F. (2011). Health effects in significant others: Separating family and care-giving effects. Medical Decision Making, 31(2), 292–298.PubMedCrossRef
10.
go back to reference Brouwer, W. B. F., Tilford, J. M., & van Exel, N. J. A. (2009). Incorporating caregiver and family effects in economic evaluations of child health. In W. Ungar (Ed.), Economic evaluation in child health. Oxford: Oxford University Press. Brouwer, W. B. F., Tilford, J. M., & van Exel, N. J. A. (2009). Incorporating caregiver and family effects in economic evaluations of child health. In W. Ungar (Ed.), Economic evaluation in child health. Oxford: Oxford University Press.
11.
go back to reference Baronet, A. M. (1999). Factors associated with caregiver burden in mental illness: a critical review of the research literature. Clinical Psychology Review, 19(7), 819–841.PubMedCrossRef Baronet, A. M. (1999). Factors associated with caregiver burden in mental illness: a critical review of the research literature. Clinical Psychology Review, 19(7), 819–841.PubMedCrossRef
12.
go back to reference Kinsella, G., Cooper, B., Picton, C., & Murtagh, D. (1998). A review of the measurement of caregiver and family burden in palliative care. Journal of Palliative Care, 14(2), 37–45.PubMed Kinsella, G., Cooper, B., Picton, C., & Murtagh, D. (1998). A review of the measurement of caregiver and family burden in palliative care. Journal of Palliative Care, 14(2), 37–45.PubMed
13.
go back to reference Vitaliano, P. P., Young, H. M., & Russo, J. (1991). Burden: a review of measures used among caregivers of individuals with dementia. The Gerontologist, 31(1), 67–75.PubMedCrossRef Vitaliano, P. P., Young, H. M., & Russo, J. (1991). Burden: a review of measures used among caregivers of individuals with dementia. The Gerontologist, 31(1), 67–75.PubMedCrossRef
14.
go back to reference Brouwer, W. B. F., van Exel, N. J. A., van Gorp, B., & Redekop, W. K. (2006). The CarerQol instrument: a new instrument to measure care-related quality of life of informal caregivers for use in economic evaluations. Quality of Life Research, 15(6), 1005–1021.PubMedCrossRef Brouwer, W. B. F., van Exel, N. J. A., van Gorp, B., & Redekop, W. K. (2006). The CarerQol instrument: a new instrument to measure care-related quality of life of informal caregivers for use in economic evaluations. Quality of Life Research, 15(6), 1005–1021.PubMedCrossRef
16.
go back to reference Beach, S. R., Schulz, R., Yee, J. L., & Jackson, S. (2000). Negative and positive health effects of caring for a disabled spouse: Longitudinal findings from the caregiver health effects study. Psychology and Aging, 15(2), 259–271.PubMedCrossRef Beach, S. R., Schulz, R., Yee, J. L., & Jackson, S. (2000). Negative and positive health effects of caring for a disabled spouse: Longitudinal findings from the caregiver health effects study. Psychology and Aging, 15(2), 259–271.PubMedCrossRef
17.
go back to reference Roth, D. L., Perkins, M., Wadley, V. G., Temple, E. M., & Haley, W. E. (2009). Family caregiving and emotional strain: associations with quality of life in a large national sample of middle-aged and older adults. Quality of Life Research, 18(6), 679–688.PubMedCrossRef Roth, D. L., Perkins, M., Wadley, V. G., Temple, E. M., & Haley, W. E. (2009). Family caregiving and emotional strain: associations with quality of life in a large national sample of middle-aged and older adults. Quality of Life Research, 18(6), 679–688.PubMedCrossRef
18.
go back to reference Schulz, R., & Beach, S. R. (1999). Caregiving as a risk factor for mortality: The caregiver health effects study. Journal of the American Medical Association, 282(23), 2215–2219.PubMedCrossRef Schulz, R., & Beach, S. R. (1999). Caregiving as a risk factor for mortality: The caregiver health effects study. Journal of the American Medical Association, 282(23), 2215–2219.PubMedCrossRef
19.
go back to reference Mohide, E. A., Torrance, G. W., Streiner, D. L., Pringle, D. M., & Gilbert, R. (1988). Measuring the wellbeing of family caregivers using the time trade-off technique. Journal of Clinical Epidemiology, 41(5), 475–482.PubMedCrossRef Mohide, E. A., Torrance, G. W., Streiner, D. L., Pringle, D. M., & Gilbert, R. (1988). Measuring the wellbeing of family caregivers using the time trade-off technique. Journal of Clinical Epidemiology, 41(5), 475–482.PubMedCrossRef
20.
go back to reference Dixon, S., Walker, M., & Salek, S. (2006). Incorporating carer effects into economic evaluation. PharmacoEconomics, 24(1), 43–53.PubMedCrossRef Dixon, S., Walker, M., & Salek, S. (2006). Incorporating carer effects into economic evaluation. PharmacoEconomics, 24(1), 43–53.PubMedCrossRef
21.
go back to reference Davidson, T., Krevers, B., & Levin, L. A. (2008). In pursuit of QALY weights for relatives: empirical estimates in relatives caring for older people. The European Journal of Health Economics, 9(3), 285–292.PubMedCrossRef Davidson, T., Krevers, B., & Levin, L. A. (2008). In pursuit of QALY weights for relatives: empirical estimates in relatives caring for older people. The European Journal of Health Economics, 9(3), 285–292.PubMedCrossRef
22.
go back to reference Basu, A., Dale, W., Elstein, A., & Meltzer, D. (2010). A time tradeoff method for eliciting partner’s quality of life due to patient’s health states in prostate cancer. Medical Decision Making, 30(3), 355–365.PubMedCrossRef Basu, A., Dale, W., Elstein, A., & Meltzer, D. (2010). A time tradeoff method for eliciting partner’s quality of life due to patient’s health states in prostate cancer. Medical Decision Making, 30(3), 355–365.PubMedCrossRef
23.
go back to reference Arafa, M. A., Zaher, S. R., El-Dowaty, A. A., & Moneeb, D. E. (2008). Quality of life among parents of children with heart disease. Health and Quality of Life Outcomes, 6, 91.PubMedCrossRef Arafa, M. A., Zaher, S. R., El-Dowaty, A. A., & Moneeb, D. E. (2008). Quality of life among parents of children with heart disease. Health and Quality of Life Outcomes, 6, 91.PubMedCrossRef
24.
go back to reference Hatzmann, J., Heymans, H. S. A., Ferrer-i-Carbonell, A., van Praag, B. M. S., & Grootenhuis, M. A. (2008). Hidden consequences of success in pediatrics: Parental health-related quality of life—Results from the care project. Pediatrics, 122(5), e1030–e1038.PubMedCrossRef Hatzmann, J., Heymans, H. S. A., Ferrer-i-Carbonell, A., van Praag, B. M. S., & Grootenhuis, M. A. (2008). Hidden consequences of success in pediatrics: Parental health-related quality of life—Results from the care project. Pediatrics, 122(5), e1030–e1038.PubMedCrossRef
25.
go back to reference Klassen, A. F., Klaassen, R., Dix, D., Pritchard, S., Yanofsky, R., O’Donnell, M., et al. (2008). Impact of caring for a child with cancer on parents’ health-related quality of life. Journal of Clinical Oncology, 26(36), 5884–5889.PubMedCrossRef Klassen, A. F., Klaassen, R., Dix, D., Pritchard, S., Yanofsky, R., O’Donnell, M., et al. (2008). Impact of caring for a child with cancer on parents’ health-related quality of life. Journal of Clinical Oncology, 26(36), 5884–5889.PubMedCrossRef
26.
go back to reference Lawoko, S., & Soares, J. J. F. (2003). Quality of life among parents of children with congenital heart disease, parents of children with other diseases and parents of healthy children. Quality of Life Research, 12(6), 655–666.PubMedCrossRef Lawoko, S., & Soares, J. J. F. (2003). Quality of life among parents of children with congenital heart disease, parents of children with other diseases and parents of healthy children. Quality of Life Research, 12(6), 655–666.PubMedCrossRef
27.
go back to reference Poley, M. J., Stolk, E. A., Langemeijer, R. A. T. M., Molenaar, J. C., & Busschbach, J. J. V. (2001). The cost-effectiveness of neonatal surgery and subsequent treatment for congenital anorectal malformations. Journal of Pediatric Surgery, 36(10), 1471–1478.PubMedCrossRef Poley, M. J., Stolk, E. A., Langemeijer, R. A. T. M., Molenaar, J. C., & Busschbach, J. J. V. (2001). The cost-effectiveness of neonatal surgery and subsequent treatment for congenital anorectal malformations. Journal of Pediatric Surgery, 36(10), 1471–1478.PubMedCrossRef
28.
go back to reference Poley, M. J., Stolk, E. A., Tibboel, D., Molenaar, J. C., & Busschbach, J. J. V. (2002). The cost-effectiveness of treatment for congenital diaphragmatic hernia. Journal of Pediatric Surgery, 37(9), 1245–1252.PubMedCrossRef Poley, M. J., Stolk, E. A., Tibboel, D., Molenaar, J. C., & Busschbach, J. J. V. (2002). The cost-effectiveness of treatment for congenital diaphragmatic hernia. Journal of Pediatric Surgery, 37(9), 1245–1252.PubMedCrossRef
29.
go back to reference Hamid, C. H., Holland, A. J. A., & Martin, H. C. O. (2007). Long-term outcome of anorectal malformations: The patient perspective. Pediatric Surgery International, 23(2), 97–102.PubMedCrossRef Hamid, C. H., Holland, A. J. A., & Martin, H. C. O. (2007). Long-term outcome of anorectal malformations: The patient perspective. Pediatric Surgery International, 23(2), 97–102.PubMedCrossRef
30.
go back to reference Hartman, E. E., Oort, F. J., Sprangers, M. A. G., Hanneman, M. J. G., van Heurn, L. W. E., de Langen, Z. J., et al. (2008). Factors affecting quality of life of children and adolescents with anorectal malformations or Hirschsprung disease. Journal of Pediatric Gastroenterology and Nutrition, 47(4), 463–471.PubMedCrossRef Hartman, E. E., Oort, F. J., Sprangers, M. A. G., Hanneman, M. J. G., van Heurn, L. W. E., de Langen, Z. J., et al. (2008). Factors affecting quality of life of children and adolescents with anorectal malformations or Hirschsprung disease. Journal of Pediatric Gastroenterology and Nutrition, 47(4), 463–471.PubMedCrossRef
31.
go back to reference Hashish, M. S., Dawoud, H. H., Hirschl, R. B., Bruch, S. W., El Batarny, A. M., Mychaliska, G. B., et al. (2010). Long-term functional outcome and quality of life in patients with high imperforate anus. Journal of Pediatric Surgery, 45(1), 224–230.PubMedCrossRef Hashish, M. S., Dawoud, H. H., Hirschl, R. B., Bruch, S. W., El Batarny, A. M., Mychaliska, G. B., et al. (2010). Long-term functional outcome and quality of life in patients with high imperforate anus. Journal of Pediatric Surgery, 45(1), 224–230.PubMedCrossRef
32.
go back to reference Ludman, L., & Spitz, L. (1995). Psychosocial adjustment of children treated for anorectal anomalies. Journal of Pediatric Surgery, 30(3), 495–499.PubMedCrossRef Ludman, L., & Spitz, L. (1995). Psychosocial adjustment of children treated for anorectal anomalies. Journal of Pediatric Surgery, 30(3), 495–499.PubMedCrossRef
33.
go back to reference Rintala, R., Mildh, L., & Lindahl, H. (1994). Fecal continence and quality of life for adult patients with an operated high or intermediate anorectal malformation. Journal of Pediatric Surgery, 29(6), 777–780.PubMedCrossRef Rintala, R., Mildh, L., & Lindahl, H. (1994). Fecal continence and quality of life for adult patients with an operated high or intermediate anorectal malformation. Journal of Pediatric Surgery, 29(6), 777–780.PubMedCrossRef
34.
go back to reference Desfrere, L., Jarreau, P. H., Dommergues, M., Brunhes, A., Hubert, P., Nihoul-Fekete, C., et al. (2000). Impact of delayed repair and elective high-frequency oscillatory ventilation on survival of antenatally diagnosed congenital diaphragmatic hernia: first application of these strategies in the more “severe” subgroup of antenatally diagnosed newborns. Intensive Care Medicine, 26(7), 934–941.PubMedCrossRef Desfrere, L., Jarreau, P. H., Dommergues, M., Brunhes, A., Hubert, P., Nihoul-Fekete, C., et al. (2000). Impact of delayed repair and elective high-frequency oscillatory ventilation on survival of antenatally diagnosed congenital diaphragmatic hernia: first application of these strategies in the more “severe” subgroup of antenatally diagnosed newborns. Intensive Care Medicine, 26(7), 934–941.PubMedCrossRef
35.
go back to reference Kays, D. W., Langham, M. R., Ledbetter, D. J., & Talbert, J. L. (1999). Detrimental effects of standard medical therapy in congenital diaphragmatic hernia. Annals of Surgery, 230(3), 340–351.PubMedCrossRef Kays, D. W., Langham, M. R., Ledbetter, D. J., & Talbert, J. L. (1999). Detrimental effects of standard medical therapy in congenital diaphragmatic hernia. Annals of Surgery, 230(3), 340–351.PubMedCrossRef
36.
go back to reference Gischler, S. J., van de Cammen-van Zijp, M. H. M., Mazer, P., Madern, G. C., Bax, N. M. A., de Jongste, J. C., et al. (2009). A prospective comparative evaluation of persistent respiratory morbidity in esophageal atresia and congenital diaphragmatic hernia survivors. Journal of Pediatric Surgery, 44(9), 1683–1690.PubMedCrossRef Gischler, S. J., van de Cammen-van Zijp, M. H. M., Mazer, P., Madern, G. C., Bax, N. M. A., de Jongste, J. C., et al. (2009). A prospective comparative evaluation of persistent respiratory morbidity in esophageal atresia and congenital diaphragmatic hernia survivors. Journal of Pediatric Surgery, 44(9), 1683–1690.PubMedCrossRef
37.
go back to reference IJsselstijn, H., Tibboel, D., Hop, W. J. C., Molenaar, J. C., & de Jongste, J. C. (1997). Long-term pulmonary sequelae in children with congenital diaphragmatic hernia. American Journal of Respiratory and Critical Care Medicine, 155(1), 174–180.PubMed IJsselstijn, H., Tibboel, D., Hop, W. J. C., Molenaar, J. C., & de Jongste, J. C. (1997). Long-term pulmonary sequelae in children with congenital diaphragmatic hernia. American Journal of Respiratory and Critical Care Medicine, 155(1), 174–180.PubMed
38.
go back to reference Nobuhara, K. K., Lund, D. P., Mitchell, J., Kharasch, V., & Wilson, J. M. (1996). Long-term outlook for survivors of congenital diaphragmatic hernia. Clinics in Perinatology, 23(4), 873–887.PubMed Nobuhara, K. K., Lund, D. P., Mitchell, J., Kharasch, V., & Wilson, J. M. (1996). Long-term outlook for survivors of congenital diaphragmatic hernia. Clinics in Perinatology, 23(4), 873–887.PubMed
39.
go back to reference Koivusalo, A., Pakarinen, M., Vanamo, K., Lindahl, H., & Rintala, R. J. (2005). Health-related quality of life in adults after repair of congenital diaphragmatic defects: a questionnaire study. Journal of Pediatric Surgery, 40(9), 1376–1381.PubMedCrossRef Koivusalo, A., Pakarinen, M., Vanamo, K., Lindahl, H., & Rintala, R. J. (2005). Health-related quality of life in adults after repair of congenital diaphragmatic defects: a questionnaire study. Journal of Pediatric Surgery, 40(9), 1376–1381.PubMedCrossRef
40.
go back to reference Peetsold, M. G., Huisman, J., Hofman, V. E., Heij, H. A., Raat, H., & Gemke, R. J. (2009). Psychological outcome and quality of life in children born with congenital diaphragmatic hernia. Archives of Disease in Childhood, 94(11), 834–840.PubMedCrossRef Peetsold, M. G., Huisman, J., Hofman, V. E., Heij, H. A., Raat, H., & Gemke, R. J. (2009). Psychological outcome and quality of life in children born with congenital diaphragmatic hernia. Archives of Disease in Childhood, 94(11), 834–840.PubMedCrossRef
41.
go back to reference Poley, M. J., Stolk, E. A., Tibboel, D., Molenaar, J. C., & Busschbach, J. J. V. (2004). Short term and long term health related quality of life after congenital anorectal malformations and congenital diaphragmatic hernia. Archives of Disease in Childhood, 89(9), 836–841.PubMedCrossRef Poley, M. J., Stolk, E. A., Tibboel, D., Molenaar, J. C., & Busschbach, J. J. V. (2004). Short term and long term health related quality of life after congenital anorectal malformations and congenital diaphragmatic hernia. Archives of Disease in Childhood, 89(9), 836–841.PubMedCrossRef
43.
go back to reference Kind, P., Hardman, G., & Macran, S. (1999). UK population norms for EQ-5D. Discussion paper 172. York: University of York—Centre for Health Economics. Kind, P., Hardman, G., & Macran, S. (1999). UK population norms for EQ-5D. Discussion paper 172. York: University of York—Centre for Health Economics.
44.
go back to reference Dolan, P. (1997). Modeling valuations for EuroQol health states. Medical Care, 35(11), 1095–1108.PubMedCrossRef Dolan, P. (1997). Modeling valuations for EuroQol health states. Medical Care, 35(11), 1095–1108.PubMedCrossRef
45.
go back to reference Luo, N., Johnson, J. A., & Coons, S. J. (2010). Using instrument-defined health state transitions to estimate minimally important differences for four preference-based health-related quality of life instruments. Medical Care, 48(4), 365–371.PubMedCrossRef Luo, N., Johnson, J. A., & Coons, S. J. (2010). Using instrument-defined health state transitions to estimate minimally important differences for four preference-based health-related quality of life instruments. Medical Care, 48(4), 365–371.PubMedCrossRef
46.
go back to reference 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(6), 1523–1532.PubMedCrossRef 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(6), 1523–1532.PubMedCrossRef
47.
go back to reference Pickard, A. S., Neary, M. P., & Cella, D. (2007). Estimation of minimally important differences in EQ-5D utility and VAS scores in cancer. Health and Quality of Life Outcomes, 5, 70.PubMedCrossRef Pickard, A. S., Neary, M. P., & Cella, D. (2007). Estimation of minimally important differences in EQ-5D utility and VAS scores in cancer. Health and Quality of Life Outcomes, 5, 70.PubMedCrossRef
48.
go back to reference Portegijs, W., Boelens, A., & Keuzenkamp, S. (2002). Emancipation Monitor 2002 [in Dutch]. The Hague: Social and Cultural Planning Office of the Netherlands, Statistics Netherlands. Portegijs, W., Boelens, A., & Keuzenkamp, S. (2002). Emancipation Monitor 2002 [in Dutch]. The Hague: Social and Cultural Planning Office of the Netherlands, Statistics Netherlands.
49.
go back to reference Schulman, J. L. (1983). Coping with major disease: child, family, pediatrician. The Journal of Pediatrics, 102(6), 988–991.PubMedCrossRef Schulman, J. L. (1983). Coping with major disease: child, family, pediatrician. The Journal of Pediatrics, 102(6), 988–991.PubMedCrossRef
50.
go back to reference Staab, D., Wenninger, K., Gebert, N., Rupprath, K., Bisson, S., Trettin, M., et al. (1998). Quality of life in patients with cystic fibrosis and their parents: What is important besides disease severity? Thorax, 53(9), 727–731.PubMedCrossRef Staab, D., Wenninger, K., Gebert, N., Rupprath, K., Bisson, S., Trettin, M., et al. (1998). Quality of life in patients with cystic fibrosis and their parents: What is important besides disease severity? Thorax, 53(9), 727–731.PubMedCrossRef
51.
go back to reference Barlow, J. H., & Ellard, D. R. (2006). The psychosocial well-being of children with chronic disease, their parents and siblings: An overview of the research evidence base. Child: Care, Health and Development, 32(1), 19–31.CrossRef Barlow, J. H., & Ellard, D. R. (2006). The psychosocial well-being of children with chronic disease, their parents and siblings: An overview of the research evidence base. Child: Care, Health and Development, 32(1), 19–31.CrossRef
52.
go back to reference Query, J. M., Reichelt, C., & Christoferson, L. A. (1990). Living with chronic illness: a retrospective study of patients shunted for hydrocephalus and their families. Developmental Medicine and Child Neurology, 32(2), 119–128.PubMedCrossRef Query, J. M., Reichelt, C., & Christoferson, L. A. (1990). Living with chronic illness: a retrospective study of patients shunted for hydrocephalus and their families. Developmental Medicine and Child Neurology, 32(2), 119–128.PubMedCrossRef
53.
go back to reference Coe, N. B., & van Houtven, C. H. (2009). Caring for mom and neglecting yourself? The health effects of caring for an elderly parent. Health Economics, 18(9), 991–1010.PubMedCrossRef Coe, N. B., & van Houtven, C. H. (2009). Caring for mom and neglecting yourself? The health effects of caring for an elderly parent. Health Economics, 18(9), 991–1010.PubMedCrossRef
54.
go back to reference Brehaut, J. C., Kohen, D. E., Raina, P., Walter, S. D., Russell, D. J., Swinton, M., et al. (2004). The health of primary caregivers of children with cerebral palsy: How does it compare with that of other Canadian caregivers? Pediatrics, 114(2), e182–e191.PubMedCrossRef Brehaut, J. C., Kohen, D. E., Raina, P., Walter, S. D., Russell, D. J., Swinton, M., et al. (2004). The health of primary caregivers of children with cerebral palsy: How does it compare with that of other Canadian caregivers? Pediatrics, 114(2), e182–e191.PubMedCrossRef
55.
go back to reference Tong, H. C., Kandala, G., Haig, A. J., Nelson, V. S., Yamakawa, K. S. J., & Shin, K. Y. (2002). Physical functioning in female caregivers of children with physical disabilities compared with female caregivers of children with a chronic medical condition. Archives of Pediatrics and Adolescent Medicine, 156(11), 1138–1142.PubMed Tong, H. C., Kandala, G., Haig, A. J., Nelson, V. S., Yamakawa, K. S. J., & Shin, K. Y. (2002). Physical functioning in female caregivers of children with physical disabilities compared with female caregivers of children with a chronic medical condition. Archives of Pediatrics and Adolescent Medicine, 156(11), 1138–1142.PubMed
56.
go back to reference Tong, H. C., Haig, A. J., Nelson, V. S., Yamakawa, K. S., Kandala, G., & Shin, K. Y. (2003). Low back pain in adult female caregivers of children with physical disabilities. Archives of Pediatrics and Adolescent Medicine, 157(11), 1128–1133.PubMedCrossRef Tong, H. C., Haig, A. J., Nelson, V. S., Yamakawa, K. S., Kandala, G., & Shin, K. Y. (2003). Low back pain in adult female caregivers of children with physical disabilities. Archives of Pediatrics and Adolescent Medicine, 157(11), 1128–1133.PubMedCrossRef
57.
go back to reference Coons, S. J., Rao, S., Keininger, D. L., & Hays, R. D. (2000). A comparative review of generic quality-of-life instruments. PharmacoEconomics, 17(1), 13–35.PubMedCrossRef Coons, S. J., Rao, S., Keininger, D. L., & Hays, R. D. (2000). A comparative review of generic quality-of-life instruments. PharmacoEconomics, 17(1), 13–35.PubMedCrossRef
58.
go back to reference Essink-Bot, M. L., Krabbe, P. F. M., Bonsel, G. J., & Aaronson, N. K. (1997). An empirical comparison of four generic health status measures. The Nottingham health profile, the medical outcomes study 36-item short-form health survey, the COOP/WONCA charts, and the EuroQol instrument. Medical Care, 35(5), 522–537.PubMedCrossRef Essink-Bot, M. L., Krabbe, P. F. M., Bonsel, G. J., & Aaronson, N. K. (1997). An empirical comparison of four generic health status measures. The Nottingham health profile, the medical outcomes study 36-item short-form health survey, the COOP/WONCA charts, and the EuroQol instrument. Medical Care, 35(5), 522–537.PubMedCrossRef
59.
go back to reference Hollingworth, W., Mackenzie, R., Todd, C. J., & Dixon, A. K. (1995). Measuring changes in quality of life following magnetic resonance imaging of the knee: SF-36, EuroQol or Rosser index? Quality of Life Research, 4(4), 325–334.PubMedCrossRef Hollingworth, W., Mackenzie, R., Todd, C. J., & Dixon, A. K. (1995). Measuring changes in quality of life following magnetic resonance imaging of the knee: SF-36, EuroQol or Rosser index? Quality of Life Research, 4(4), 325–334.PubMedCrossRef
60.
go back to reference Myers, C., & Wilks, D. (1999). Comparison of Euroqol EQ-5D and SF-36 in patients with chronic fatigue syndrome. Quality of Life Research, 8(1–2), 9–16.PubMedCrossRef Myers, C., & Wilks, D. (1999). Comparison of Euroqol EQ-5D and SF-36 in patients with chronic fatigue syndrome. Quality of Life Research, 8(1–2), 9–16.PubMedCrossRef
61.
go back to reference Cohen, C. A., Colantonio, A., & Vernich, L. (2002). Positive aspects of caregiving: rounding out the caregiver experience. International Journal of Geriatric Psychiatry, 17(2), 184–188.PubMedCrossRef Cohen, C. A., Colantonio, A., & Vernich, L. (2002). Positive aspects of caregiving: rounding out the caregiver experience. International Journal of Geriatric Psychiatry, 17(2), 184–188.PubMedCrossRef
62.
go back to reference Lawton, M. P., Kleban, M. H., Moss, M., Rovine, M., & Glicksman, A. (1989). Measuring caregiving appraisal. Journal of Gerontology, 44(3), P61–P71.PubMed Lawton, M. P., Kleban, M. H., Moss, M., Rovine, M., & Glicksman, A. (1989). Measuring caregiving appraisal. Journal of Gerontology, 44(3), P61–P71.PubMed
63.
go back to reference Motenko, A. K. (1989). The frustrations, gratifications, and well-being of dementia caregivers. The Gerontologist, 29(2), 166–172.PubMedCrossRef Motenko, A. K. (1989). The frustrations, gratifications, and well-being of dementia caregivers. The Gerontologist, 29(2), 166–172.PubMedCrossRef
64.
go back to reference Brouwer, W. B. F., van Exel, N. J. A., van den Berg, B., van de Bos, G. A., & Koopmanschap, M. A. (2005). Process utility from providing informal care: The benefit of caring. Health Policy, 74(1), 85–99.PubMedCrossRef Brouwer, W. B. F., van Exel, N. J. A., van den Berg, B., van de Bos, G. A., & Koopmanschap, M. A. (2005). Process utility from providing informal care: The benefit of caring. Health Policy, 74(1), 85–99.PubMedCrossRef
65.
go back to reference Centraal Bureau voor de Statistiek. (2000). Werken en leren 2000–2001. Feiten en cijfers over de arbeidsmarkt en het onderwijs in Nederland. Samsom: Alphen aan den Rijn. Centraal Bureau voor de Statistiek. (2000). Werken en leren 2000–2001. Feiten en cijfers over de arbeidsmarkt en het onderwijs in Nederland. Samsom: Alphen aan den Rijn.
Metadata
Title
Assessing health-related quality-of-life changes in informal caregivers: an evaluation in parents of children with major congenital anomalies
Authors
Marten J. Poley
Werner B. F. Brouwer
N. Job A. van Exel
Dick Tibboel
Publication date
01-06-2012
Publisher
Springer Netherlands
Published in
Quality of Life Research / Issue 5/2012
Print ISSN: 0962-9343
Electronic ISSN: 1573-2649
DOI
https://doi.org/10.1007/s11136-011-9991-7

Other articles of this Issue 5/2012

Quality of Life Research 5/2012 Go to the issue