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Gepubliceerd in: Quality of Life Research 8/2013

01-10-2013 | Review

Condition-specific quality of life questionnaires for caregivers of children with pediatric conditions: a systematic review

Auteurs: Maria Yui Kwan Chow, Angela M. Morrow, Spring Chenoa Cooper Robbins, Julie Leask

Gepubliceerd in: Quality of Life Research | Uitgave 8/2013

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Abstract

Purpose

Childhood illness or disability can affect the quality of life (QoL) of the child’s primary caregiver. Our aim was to identify, describe the content and systematically review the psychometric properties of condition-specific QoL questionnaires for caregivers of children.

Methods

Medline, PsycInfo, Embase, CINAHL, and the Cochrane library databases were searched from 1 January 1990 to 30 June 2011. Articles related to the development and measurement of caregiver QoL were screened to identify condition-specific questionnaires. The characteristics of the questionnaires were extracted, and their psychometric properties were evaluated using the consensus-based standards for the selection of health measurement instruments checklist with 4-point scale.

Results

We identified 25 condition-specific caregiver QoL questionnaires covering 16 conditions. Conditions included atopic dermatitis, asthma, diabetes, oro-facial disorders, and two acute illnesses. Questionnaires were developed predominantly in high-income countries. Questionnaires had the highest quality rating for content validity, followed by hypothesis testing. Methodological quality was satisfactory for criterion validity; fair in reliability and responsiveness; and poor in internal consistency and structural validity.

Conclusions

The increasing number of questionnaires developed over time shows improved recognition of the importance of caregiver QoL. There is a paucity of QoL questionnaires for caregivers of otherwise healthy children suffering from physical injuries and acute conditions associated with significant caregiver burden. Cultural validation of existing and new questionnaires in lower-income countries is necessary. Data collected by condition-specific questionnaires can assist clinicians and health economists in estimating caregiver burden and the types of healthcare services caregivers require and may be useful for healthcare administrators to evaluate interventions.
Literatuur
1.
go back to reference Bode, H., Weidner, K., & Storck, M. (2000). Quality of life in families of children with disabilities. Developmental Medicine and Child Neurology, 42(5), 354.PubMedCrossRef Bode, H., Weidner, K., & Storck, M. (2000). Quality of life in families of children with disabilities. Developmental Medicine and Child Neurology, 42(5), 354.PubMedCrossRef
2.
go back to reference Davis, E., Shelly, A., Waters, E., et al. (2010). The impact of caring for a child with cerebral palsy: quality of life for mothers and fathers. Child: Care, Health and Development, 36(1), 63–73.CrossRef Davis, E., Shelly, A., Waters, E., et al. (2010). The impact of caring for a child with cerebral palsy: quality of life for mothers and fathers. Child: Care, Health and Development, 36(1), 63–73.CrossRef
3.
go back to reference Von Essen, L., Sjoden, P. O., & Mattsson, E. (2004). Swedish mothers and fathers of a child diagnosed with cancer: A look at their quality of life. Acta Oncologica, 5, 474–479.CrossRef Von Essen, L., Sjoden, P. O., & Mattsson, E. (2004). Swedish mothers and fathers of a child diagnosed with cancer: A look at their quality of life. Acta Oncologica, 5, 474–479.CrossRef
4.
go back to reference Basra, M. K., & Finlay, A. Y. (2007). The family impact of skin diseases: The Greater Patient concept. British Journal of Dermatology, 156(5), 929–937.PubMedCrossRef Basra, M. K., & Finlay, A. Y. (2007). The family impact of skin diseases: The Greater Patient concept. British Journal of Dermatology, 156(5), 929–937.PubMedCrossRef
5.
go back to reference Perkins, S., Winn, S., Murray, J., et al. (2004). A qualitative study of the experience of caring for a person with bulimia nervosa. Part 1: The emotional impact of caring. International Journal of Eating Disorders, 36(3), 256–268.PubMedCrossRef Perkins, S., Winn, S., Murray, J., et al. (2004). A qualitative study of the experience of caring for a person with bulimia nervosa. Part 1: The emotional impact of caring. International Journal of Eating Disorders, 36(3), 256–268.PubMedCrossRef
6.
go back to reference Punpanich, W, Gorbach, P. M., & Detels, R. (2011). Impact of paediatric human immunodeficiency virus infection on children’s and caregivers’ daily functioning and well-being: a qualitative study. Child Care Health Dev. doi:10.1111/j.1365-2214.2011.01301.x. Punpanich, W, Gorbach, P. M., & Detels, R. (2011). Impact of paediatric human immunodeficiency virus infection on children’s and caregivers’ daily functioning and well-being: a qualitative study. Child Care Health Dev. doi:10.​1111/​j.​1365-2214.​2011.​01301.​x.
7.
go back to reference Duguid, A., Morrison, S., Robertson, A., et al. (2007). The psychological impact of genital anomalies on the parents of affected children. Acta Paediatrica, 96(3), 348–352.PubMedCrossRef Duguid, A., Morrison, S., Robertson, A., et al. (2007). The psychological impact of genital anomalies on the parents of affected children. Acta Paediatrica, 96(3), 348–352.PubMedCrossRef
8.
go back to reference Knock, J., Kline, E., Schiffman, J., et al. (2011). Burdens and difficulties experienced by caregivers of children and adolescents with schizophrenia-spectrum disorders: a qualitative study. Early Intervention in Psychiatry, 5(4), 349–354.PubMedCrossRef Knock, J., Kline, E., Schiffman, J., et al. (2011). Burdens and difficulties experienced by caregivers of children and adolescents with schizophrenia-spectrum disorders: a qualitative study. Early Intervention in Psychiatry, 5(4), 349–354.PubMedCrossRef
9.
go back to reference Edmonds-Myles, S., Tamborlane, W. V., & Grey, M. (2010). Perception of the impact of type 1 diabetes on low-income families. The Diabetes Educator, 36(2), 318–325.PubMedCrossRef Edmonds-Myles, S., Tamborlane, W. V., & Grey, M. (2010). Perception of the impact of type 1 diabetes on low-income families. The Diabetes Educator, 36(2), 318–325.PubMedCrossRef
10.
go back to reference Vandagriff, J. L., Marrero, D. G., Ingersoll, G. M., et al. (1992). Parents of children with diabetes: what are they worried about? The Diabetes Educator, 18(4), 299–302.PubMedCrossRef Vandagriff, J. L., Marrero, D. G., Ingersoll, G. M., et al. (1992). Parents of children with diabetes: what are they worried about? The Diabetes Educator, 18(4), 299–302.PubMedCrossRef
11.
go back to reference Sparacino, P. S., Tong, E. M., Messias, D. K., et al. (1997). The dilemmas of parents of adolescents and young adults with congenital heart disease. Heart and Lung, 26(3), 187–195.PubMedCrossRef Sparacino, P. S., Tong, E. M., Messias, D. K., et al. (1997). The dilemmas of parents of adolescents and young adults with congenital heart disease. Heart and Lung, 26(3), 187–195.PubMedCrossRef
12.
go back to reference Byles, J., Byrne, C., Boyle, M. H., et al. (1988). Ontario Child Health Study: Reliability and validity of the general functioning subscale of the McMaster family assessment device. Family Process, 27(1), 97–104.PubMedCrossRef Byles, J., Byrne, C., Boyle, M. H., et al. (1988). Ontario Child Health Study: Reliability and validity of the general functioning subscale of the McMaster family assessment device. Family Process, 27(1), 97–104.PubMedCrossRef
13.
go back to reference Lv R-j, Wu., L-w, Jin. L.-r., et al. (2009). Reliability and validity of a Chinese version of the Impact of Pediatric Epilepsy Scale. Epilepsy & Behavior, 16(1), 150–155.CrossRef Lv R-j, Wu., L-w, Jin. L.-r., et al. (2009). Reliability and validity of a Chinese version of the Impact of Pediatric Epilepsy Scale. Epilepsy & Behavior, 16(1), 150–155.CrossRef
14.
go back to reference McCubbin, H. I., et al. (1983). CHIP–coping health inventory for parents: An assessment of parental coping patterns in the care of the chronically ill child. Journal of Marriage and the Family, 45(2), 359–370.CrossRef McCubbin, H. I., et al. (1983). CHIP–coping health inventory for parents: An assessment of parental coping patterns in the care of the chronically ill child. Journal of Marriage and the Family, 45(2), 359–370.CrossRef
15.
go back to reference Pearlin, L. I., & Schooler, C. (1978). The structure of coping. Journal of Health and Social Behavior, 19(1), 2–21.PubMedCrossRef Pearlin, L. I., & Schooler, C. (1978). The structure of coping. Journal of Health and Social Behavior, 19(1), 2–21.PubMedCrossRef
16.
go back to reference Spielberger, C. D., Gorssuch, R. L., Lushene, P. R., et al. (1983). Manual for the state-trait anxiety inventory (1st ed.). Palo Alto, CA: Consulting Psychologists Press. Spielberger, C. D., Gorssuch, R. L., Lushene, P. R., et al. (1983). Manual for the state-trait anxiety inventory (1st ed.). Palo Alto, CA: Consulting Psychologists Press.
17.
go back to reference Streisand, R., Braniecki, S., Tercyak, K. P., et al. (2001). Childhood illness-related parenting stress: The Pediatric Inventory for Parents. Journal of Pediatric Psychology, 26(3), 155–162.PubMedCrossRef Streisand, R., Braniecki, S., Tercyak, K. P., et al. (2001). Childhood illness-related parenting stress: The Pediatric Inventory for Parents. Journal of Pediatric Psychology, 26(3), 155–162.PubMedCrossRef
18.
go back to reference Hoffman, L., Marquis, J., Poston, D., et al. (2006). Assessing family outcomes: psychometric evaluation of the Beach Center Family Quality of Life Scale. Journal of Marriage and the Family, 68(4), 1069–1083.CrossRef Hoffman, L., Marquis, J., Poston, D., et al. (2006). Assessing family outcomes: psychometric evaluation of the Beach Center Family Quality of Life Scale. Journal of Marriage and the Family, 68(4), 1069–1083.CrossRef
19.
go back to reference Werner, S., Edwards, M., Baum, N., et al. (2009). Family quality of life among families with a member who has an intellectual disability: An exploratory examination of key domains and dimensions of the revised FQOL Survey. Journal of Intellectual Disability Research, 53(6), 501–511.PubMedCrossRef Werner, S., Edwards, M., Baum, N., et al. (2009). Family quality of life among families with a member who has an intellectual disability: An exploratory examination of key domains and dimensions of the revised FQOL Survey. Journal of Intellectual Disability Research, 53(6), 501–511.PubMedCrossRef
20.
go back to reference Davis, E., Waters, E., Mackinnon, A., et al. (2006). Paediatric quality of life instruments: a review of the impact of the conceptual framework on outcomes. Developmental Medicine and Child Neurology, 48(4), 311–318.PubMedCrossRef Davis, E., Waters, E., Mackinnon, A., et al. (2006). Paediatric quality of life instruments: a review of the impact of the conceptual framework on outcomes. Developmental Medicine and Child Neurology, 48(4), 311–318.PubMedCrossRef
21.
go back to reference De Civita, M., Regier, D., Alamgir, A. H., et al. (2005). Evaluating health-related quality-of-life studies in paediatric populations: some conceptual, methodological and developmental considerations and recent applications. Pharmacoeconomics, 23(7), 659–685.PubMedCrossRef De Civita, M., Regier, D., Alamgir, A. H., et al. (2005). Evaluating health-related quality-of-life studies in paediatric populations: some conceptual, methodological and developmental considerations and recent applications. Pharmacoeconomics, 23(7), 659–685.PubMedCrossRef
23.
go back to reference Donohue, P. K. (2002). Health-related quality of life of preterm children and their caregivers. Mental Retardation and Developmental Disabilities Research Reviews, 8(4), 293–297.PubMedCrossRef Donohue, P. K. (2002). Health-related quality of life of preterm children and their caregivers. Mental Retardation and Developmental Disabilities Research Reviews, 8(4), 293–297.PubMedCrossRef
24.
go back to reference McKenna, S. P., & Doward, L. C. (2008). Quality of life of children with atopic dermatitis and their families. Current opinion in Allergy and Clinical Immunology, 8(3), 228–231.PubMedCrossRef McKenna, S. P., & Doward, L. C. (2008). Quality of life of children with atopic dermatitis and their families. Current opinion in Allergy and Clinical Immunology, 8(3), 228–231.PubMedCrossRef
26.
go back to reference Morrow, A. M., Quine, S., Heaton, M. D., et al. (2010). Assessing quality of life in paediatric clinical practice. Journal of Paediatrics and Child Health, 46(6), 323–328.PubMedCrossRef Morrow, A. M., Quine, S., Heaton, M. D., et al. (2010). Assessing quality of life in paediatric clinical practice. Journal of Paediatrics and Child Health, 46(6), 323–328.PubMedCrossRef
27.
go back to reference Arafa, M. A., Zaher, S. R., El Dowaty, A. A., et al. (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., et al. (2008). Quality of life among parents of children with heart disease. Health and Quality of Life Outcomes, 6, 91.PubMedCrossRef
28.
go back to reference Chien, L. Y., Lo, L. H., Chen, C. J., et al. (2003). Quality of life among primary caregivers of Taiwanese children with brain tumor. Cancer Nursing, 26(4), 305–311.PubMedCrossRef Chien, L. Y., Lo, L. H., Chen, C. J., et al. (2003). Quality of life among primary caregivers of Taiwanese children with brain tumor. Cancer Nursing, 26(4), 305–311.PubMedCrossRef
29.
go back to reference Brisson, M., Senecal, M., Drolet, M., et al. (2010). Health-related quality of life lost to rotavirus-associated gastroenteritis in children and their parents: A canadian prospective study. The Pediatric Infectious Disease Journal, 29(1), 73–75.PubMedCrossRef Brisson, M., Senecal, M., Drolet, M., et al. (2010). Health-related quality of life lost to rotavirus-associated gastroenteritis in children and their parents: A canadian prospective study. The Pediatric Infectious Disease Journal, 29(1), 73–75.PubMedCrossRef
30.
go back to reference Van, D. T. X., Hatzmann, J., Ensink, E., et al. (2008). Quality of life of female caregivers of children with sickle cell disease: A survey. Haematologica, 94(4), 588–593. Van, D. T. X., Hatzmann, J., Ensink, E., et al. (2008). Quality of life of female caregivers of children with sickle cell disease: A survey. Haematologica, 94(4), 588–593.
31.
go back to reference Solans, M., Pane, S., Estrada, M. D., et al. (2008). Health-related quality of life measurement in children and adolescents: A systematic review of generic and disease-specific instruments. Value Health, 11(4), 742–764.PubMedCrossRef Solans, M., Pane, S., Estrada, M. D., et al. (2008). Health-related quality of life measurement in children and adolescents: A systematic review of generic and disease-specific instruments. Value Health, 11(4), 742–764.PubMedCrossRef
32.
go back to reference Wiebe, S., Guyatt, G., Weaver, B., et al. (2003). Comparative responsiveness of generic and specific quality-of-life instruments. Journal of Clinical Epidemiology, 56(1), 52–60.PubMedCrossRef Wiebe, S., Guyatt, G., Weaver, B., et al. (2003). Comparative responsiveness of generic and specific quality-of-life instruments. Journal of Clinical Epidemiology, 56(1), 52–60.PubMedCrossRef
33.
go back to reference Bowden, A., & Fox-Rushby, J. A. (2003). A systematic and critical review of the process of translation and adaptation of generic health-related quality of life measures in Africa, Asia, Eastern Europe, the Middle East, South America. Social Science and Medicine, 57(7), 1289–1306.PubMedCrossRef Bowden, A., & Fox-Rushby, J. A. (2003). A systematic and critical review of the process of translation and adaptation of generic health-related quality of life measures in Africa, Asia, Eastern Europe, the Middle East, South America. Social Science and Medicine, 57(7), 1289–1306.PubMedCrossRef
34.
go back to reference Coons, S. J., Rao, S., Keininger, D. L., et al. (2000). A comparative review of generic quality-of-life instruments. Pharmacoeconomics, 17(1), 13–35.PubMedCrossRef Coons, S. J., Rao, S., Keininger, D. L., et al. (2000). A comparative review of generic quality-of-life instruments. Pharmacoeconomics, 17(1), 13–35.PubMedCrossRef
35.
go back to reference Riley, A. W., Lyman, L. M., Spiel, G., et al. (2006). The Family Strain Index (FSI). Reliability, validity, and factor structure of a brief questionnaire for families of children with ADHD. European Child and Adolescent Psychiatry, 15(Supp1), i72–i78. Riley, A. W., Lyman, L. M., Spiel, G., et al. (2006). The Family Strain Index (FSI). Reliability, validity, and factor structure of a brief questionnaire for families of children with ADHD. European Child and Adolescent Psychiatry, 15(Supp1), i72–i78.
36.
go back to reference Abidin, R. R. (1990). Parenting Stress Index Short Form: Test manual. Charlottesville: Pediatric Psychology. Abidin, R. R. (1990). Parenting Stress Index Short Form: Test manual. Charlottesville: Pediatric Psychology.
37.
go back to reference Lohr, K. N., Aaronson, N. K., Alonso, J., et al. (1996). Evaluating quality-of-life and health status instruments: development of scientific review criteria. Clinical Therapeutics, 18(5), 979–992.PubMedCrossRef Lohr, K. N., Aaronson, N. K., Alonso, J., et al. (1996). Evaluating quality-of-life and health status instruments: development of scientific review criteria. Clinical Therapeutics, 18(5), 979–992.PubMedCrossRef
38.
go back to reference Terwee, C. B., Mokkink, L. B., Patrick, D. L., et al. (2012). Rating the methodological quality in systematic reviews of studies on measurement properties: a scoring system for the COSMIN checklist. Quality of Life Research, 21, 651–657.PubMedCrossRef Terwee, C. B., Mokkink, L. B., Patrick, D. L., et al. (2012). Rating the methodological quality in systematic reviews of studies on measurement properties: a scoring system for the COSMIN checklist. Quality of Life Research, 21, 651–657.PubMedCrossRef
39.
go back to reference Basra, M. K., Sue-Ho, R., & Finlay, A. Y. (2007). The Family Dermatology Life Quality Index: measuring the secondary impact of skin disease. The British Journal of Dermatology, 156(3), 528–538.PubMedCrossRef Basra, M. K., Sue-Ho, R., & Finlay, A. Y. (2007). The Family Dermatology Life Quality Index: measuring the secondary impact of skin disease. The British Journal of Dermatology, 156(3), 528–538.PubMedCrossRef
40.
go back to reference Chamlin, S. L., Cella, D., Frieden, I. J., et al. (2005). Development of the childhood atopic dermatitis impact scale: Initial validation of a quality-of-life measure for young children with atopic dermatitis and their families. The Journal of Investigative Dermatology, 125(6), 1106–1111.PubMedCrossRef Chamlin, S. L., Cella, D., Frieden, I. J., et al. (2005). Development of the childhood atopic dermatitis impact scale: Initial validation of a quality-of-life measure for young children with atopic dermatitis and their families. The Journal of Investigative Dermatology, 125(6), 1106–1111.PubMedCrossRef
41.
go back to reference Chamlin, S. L., Lai, J. S., Cella, D., et al. (2007). Childhood atopic dermatitis impact scale: Reliability, discriminative and concurrent validity, and responsiveness. Archives of Dermatology, 143(6), 768–772.PubMedCrossRef Chamlin, S. L., Lai, J. S., Cella, D., et al. (2007). Childhood atopic dermatitis impact scale: Reliability, discriminative and concurrent validity, and responsiveness. Archives of Dermatology, 143(6), 768–772.PubMedCrossRef
42.
go back to reference Kondo-Endo, K., Ohashi, Y., Nakagawa, H., et al. (2009). Development and validation of a questionnaire measuring quality of life in primary caregivers of children with atopic dermatitis (QPCAD). British Journal of Dermatology, 161(3), 617–625.PubMedCrossRef Kondo-Endo, K., Ohashi, Y., Nakagawa, H., et al. (2009). Development and validation of a questionnaire measuring quality of life in primary caregivers of children with atopic dermatitis (QPCAD). British Journal of Dermatology, 161(3), 617–625.PubMedCrossRef
43.
go back to reference Lawson, V., Lewis-Jones, M. S., Finlay, A. Y., et al. (1998). The family impact of childhood atopic dermatitis: the Dermatitis Family Impact Questionnaire. British Journal of Dermatology, 138(1), 107–113.PubMedCrossRef Lawson, V., Lewis-Jones, M. S., Finlay, A. Y., et al. (1998). The family impact of childhood atopic dermatitis: the Dermatitis Family Impact Questionnaire. British Journal of Dermatology, 138(1), 107–113.PubMedCrossRef
44.
go back to reference McKenna, S. P., Whalley, D., Dewar, A. L., et al. (2005). International development of the Parents’ Index of Quality of Life in Atopic Dermatitis (PIQoL-AD). Quality of Life Research, 14(1), 231–241.PubMedCrossRef McKenna, S. P., Whalley, D., Dewar, A. L., et al. (2005). International development of the Parents’ Index of Quality of Life in Atopic Dermatitis (PIQoL-AD). Quality of Life Research, 14(1), 231–241.PubMedCrossRef
45.
go back to reference Juniper, E. F., Guyatt, G. H., Feeny, D. H., et al. (1996). Measuring quality of life in the parents of children with asthma. Quality of Life Research, 5(1), 27–34.PubMedCrossRef Juniper, E. F., Guyatt, G. H., Feeny, D. H., et al. (1996). Measuring quality of life in the parents of children with asthma. Quality of Life Research, 5(1), 27–34.PubMedCrossRef
46.
go back to reference Schulz, R. M., Dye, J., Jolicoeur, L., et al. (1994). Quality-of-life factors for parents of children with asthma. Journal of Asthma, 31(3), 209–219.PubMedCrossRef Schulz, R. M., Dye, J., Jolicoeur, L., et al. (1994). Quality-of-life factors for parents of children with asthma. Journal of Asthma, 31(3), 209–219.PubMedCrossRef
47.
go back to reference Forns, D., Prat, R., & Tauler, E. (2011). Evaluation of quality of life among the caregivers of asthmatic children: The new IFABI-R questionnaire. Allergologia et Immunopathologia, 39(1), 32–38.PubMedCrossRef Forns, D., Prat, R., & Tauler, E. (2011). Evaluation of quality of life among the caregivers of asthmatic children: The new IFABI-R questionnaire. Allergologia et Immunopathologia, 39(1), 32–38.PubMedCrossRef
48.
go back to reference Cappelleri, J. C., Gerber, R. A., Quattrin, T., et al. (2008). Development and validation of the WEll-being and Satisfaction of CAREgivers of Children with Diabetes Questionnaire (WE-CARE). Health and Quality of Life Outcomes, 6, 3.PubMedCrossRef Cappelleri, J. C., Gerber, R. A., Quattrin, T., et al. (2008). Development and validation of the WEll-being and Satisfaction of CAREgivers of Children with Diabetes Questionnaire (WE-CARE). Health and Quality of Life Outcomes, 6, 3.PubMedCrossRef
49.
go back to reference Faulkner, M. S., & Clark, F. S. (1998). Quality of life for parents of children and adolescents with type 1 diabetes. The Diabetes Educator, 24(6), 721–727.PubMedCrossRef Faulkner, M. S., & Clark, F. S. (1998). Quality of life for parents of children and adolescents with type 1 diabetes. The Diabetes Educator, 24(6), 721–727.PubMedCrossRef
50.
go back to reference Locker, D., Jokovic, A., Stephens, M., et al. (2002). Family impact of child oral and oro-facial conditions. Community Dentistry and Oral Epidemiology, 30(6), 438–448.PubMedCrossRef Locker, D., Jokovic, A., Stephens, M., et al. (2002). Family impact of child oral and oro-facial conditions. Community Dentistry and Oral Epidemiology, 30(6), 438–448.PubMedCrossRef
51.
go back to reference Patjanasoontorn, N., Pradubwong, S., Mongkoltawornchai, S., et al. (2010). Development and reliability of the THAICLEFT Quality of Life Questionnaire for children with cleft lip/palate and families. Journal of the Medical Association of Thailand, 93(Suppl 4), S16–S18.PubMed Patjanasoontorn, N., Pradubwong, S., Mongkoltawornchai, S., et al. (2010). Development and reliability of the THAICLEFT Quality of Life Questionnaire for children with cleft lip/palate and families. Journal of the Medical Association of Thailand, 93(Suppl 4), S16–S18.PubMed
52.
go back to reference Dube, E., De Wals, P., & Ouakki, M. (2010). Quality of life of children and their caregivers during an AOM episode: development and use of a telephone questionnaire. Health and Quality of Life Outcomes, 8, 75.PubMedCrossRef Dube, E., De Wals, P., & Ouakki, M. (2010). Quality of life of children and their caregivers during an AOM episode: development and use of a telephone questionnaire. Health and Quality of Life Outcomes, 8, 75.PubMedCrossRef
53.
go back to reference Berdeaux, G., Hervie, C., Smajda, C., et al. (1998). Parental quality of life and recurrent ENT infections in their children: development of a questionnaire. Rhinitis Survey Group. Quality of Life Research, 7(6), 501–512.PubMedCrossRef Berdeaux, G., Hervie, C., Smajda, C., et al. (1998). Parental quality of life and recurrent ENT infections in their children: development of a questionnaire. Rhinitis Survey Group. Quality of Life Research, 7(6), 501–512.PubMedCrossRef
54.
go back to reference Weitzner, M. A., Jacobsen, P. B., Wagner, H., Jr, et al. (1999). The Caregiver Quality of Life Index-Cancer (CQOLC) scale: development and validation of an instrument to measure quality of life of the family caregiver of patients with cancer. Quality of Life Research, 8(1–2), 55–63.PubMedCrossRef Weitzner, M. A., Jacobsen, P. B., Wagner, H., Jr, et al. (1999). The Caregiver Quality of Life Index-Cancer (CQOLC) scale: development and validation of an instrument to measure quality of life of the family caregiver of patients with cancer. Quality of Life Research, 8(1–2), 55–63.PubMedCrossRef
55.
go back to reference Farnik, M., Brozek, G., Pierzchala, W., et al. (2010). Development, evaluation and validation of a new instrument for measurement quality of life in the parents of children with chronic disease. Health and Quality of Life Outcomes, 8, 151.PubMedCrossRef Farnik, M., Brozek, G., Pierzchala, W., et al. (2010). Development, evaluation and validation of a new instrument for measurement quality of life in the parents of children with chronic disease. Health and Quality of Life Outcomes, 8, 151.PubMedCrossRef
56.
go back to reference Mazer, P., Gischler, S. J., Koot, H. M., et al. (2008). Impact of a child with congenital anomalies on parents (ICCAP) questionnaire; a psychometric analysis. Health and Quality of Life Outcomes, 6, 102. doi:10.1186/1477-7525-6-102. Mazer, P., Gischler, S. J., Koot, H. M., et al. (2008). Impact of a child with congenital anomalies on parents (ICCAP) questionnaire; a psychometric analysis. Health and Quality of Life Outcomes, 6, 102. doi:10.​1186/​1477-7525-6-102.
57.
go back to reference Boling, W., Macrina, D. M., & Clancy, J. P. (2003). The Caregiver Quality of Life Cystic Fibrosis (CQOLCF) scale: modification and validation of an instrument to measure quality of life in cystic fibrosis family caregivers. Quality of Life Research, 12(8), 1119–1126.PubMedCrossRef Boling, W., Macrina, D. M., & Clancy, J. P. (2003). The Caregiver Quality of Life Cystic Fibrosis (CQOLCF) scale: modification and validation of an instrument to measure quality of life in cystic fibrosis family caregivers. Quality of Life Research, 12(8), 1119–1126.PubMedCrossRef
58.
go back to reference Camfield, C., Breau, L., & Camfield, P. (2001). Impact of pediatric epilepsy on the family: a new scale for clinical and research use. Epilepsia, 42(1), 104–112.PubMedCrossRef Camfield, C., Breau, L., & Camfield, P. (2001). Impact of pediatric epilepsy on the family: a new scale for clinical and research use. Epilepsia, 42(1), 104–112.PubMedCrossRef
59.
go back to reference Barnard, D., Woloski, M., Feeny, D., et al. (2003). Development of disease-specific health-related quality-of-life instruments for children with immune thrombocytopenic purpura and their parents. Journal of Pediatric Hematology/oncology, 25(1), 56–62.PubMedCrossRef Barnard, D., Woloski, M., Feeny, D., et al. (2003). Development of disease-specific health-related quality-of-life instruments for children with immune thrombocytopenic purpura and their parents. Journal of Pediatric Hematology/oncology, 25(1), 56–62.PubMedCrossRef
60.
go back to reference Hatt, S. R., Leske, D. A., Yamada, T., et al. (2010). Development and initial validation of quality-of-life questionnaires for intermittent exotropia. Ophthalmology, 117(1), 163–168.PubMedCrossRef Hatt, S. R., Leske, D. A., Yamada, T., et al. (2010). Development and initial validation of quality-of-life questionnaires for intermittent exotropia. Ophthalmology, 117(1), 163–168.PubMedCrossRef
61.
go back to reference Matsumoto, H., Clayton-Krasinski, D. A., Klinge, S. A., et al. (2011). Development and initial validation of the assessment of caregiver experience with neuromuscular disease. Journal of Pediatric Orthopedics, 31(3), 284–292.PubMedCrossRef Matsumoto, H., Clayton-Krasinski, D. A., Klinge, S. A., et al. (2011). Development and initial validation of the assessment of caregiver experience with neuromuscular disease. Journal of Pediatric Orthopedics, 31(3), 284–292.PubMedCrossRef
62.
go back to reference Bachmann, C., Ackmann, C., Janhsen, E., et al. (2010). Clinical evaluation of the short-form pediatric enuresis module to assess quality of life. Neurourology and Urodynamics, 29(8), 1397–1402.PubMedCrossRef Bachmann, C., Ackmann, C., Janhsen, E., et al. (2010). Clinical evaluation of the short-form pediatric enuresis module to assess quality of life. Neurourology and Urodynamics, 29(8), 1397–1402.PubMedCrossRef
63.
go back to reference Cohen, B. L., Noone, S., Munoz-Furlong, A., et al. (2004). Development of a questionnaire to measure quality of life in families with a child with food allergy. The Journal of Allergy and Clinical Immunology, 114(5), 1159–1163.PubMedCrossRef Cohen, B. L., Noone, S., Munoz-Furlong, A., et al. (2004). Development of a questionnaire to measure quality of life in families with a child with food allergy. The Journal of Allergy and Clinical Immunology, 114(5), 1159–1163.PubMedCrossRef
64.
go back to reference Caples, M., & Sweeney, J. (2011). Quality of life: A survey of parents of children/adults with an intellectual disability who are availing of respite care. British Journal of Learning Disabilities, 39(1), 64–72. Caples, M., & Sweeney, J. (2011). Quality of life: A survey of parents of children/adults with an intellectual disability who are availing of respite care. British Journal of Learning Disabilities, 39(1), 64–72.
65.
go back to reference Breau, G. M., Camfield, C. S., Camfield, P. R., et al. (2008). Evaluation of the responsiveness of the Impact of Pediatric Epilepsy Scale. Epilepsy & Behavior, 13(3), 454–457.CrossRef Breau, G. M., Camfield, C. S., Camfield, P. R., et al. (2008). Evaluation of the responsiveness of the Impact of Pediatric Epilepsy Scale. Epilepsy & Behavior, 13(3), 454–457.CrossRef
66.
go back to reference Kunz, B., Oranje, A. P., Labreze, L., et al. (1997). Clinical validation and guidelines for the SCORAD index: Consensus report of the European Task Force on Atopic Dermatitis. Dermatology, 195(1), 10–19.PubMedCrossRef Kunz, B., Oranje, A. P., Labreze, L., et al. (1997). Clinical validation and guidelines for the SCORAD index: Consensus report of the European Task Force on Atopic Dermatitis. Dermatology, 195(1), 10–19.PubMedCrossRef
67.
go back to reference Ware, J. E., Jr. (1992). Sherbourne CD. The MOS 36-item short-form health survey (SF-36). Conceptual framework and item selection. Medical Care, 30(6), 473–483.PubMedCrossRef Ware, J. E., Jr. (1992). Sherbourne CD. The MOS 36-item short-form health survey (SF-36). Conceptual framework and item selection. Medical Care, 30(6), 473–483.PubMedCrossRef
69.
go back to reference Stein, R. E., & Riessman, C. K. (1980). The development of an impact-on-family scale: Preliminary findings. Medical Care, 18(4), 465–472.PubMedCrossRef Stein, R. E., & Riessman, C. K. (1980). The development of an impact-on-family scale: Preliminary findings. Medical Care, 18(4), 465–472.PubMedCrossRef
70.
go back to reference Hunt, S. M., & McKenna, S. P. (1992). A british adaptation of the general well-being index: A new tool for clinical research. British Journal of Medical Economics, 2, 49–60. Hunt, S. M., & McKenna, S. P. (1992). A british adaptation of the general well-being index: A new tool for clinical research. British Journal of Medical Economics, 2, 49–60.
71.
go back to reference Landgraf, J. L., Abetz, L., & Ware, J. E. (1996). The CHQ user’s manual. Boston: The Health Institute, New England medical Center. Landgraf, J. L., Abetz, L., & Ware, J. E. (1996). The CHQ user’s manual. Boston: The Health Institute, New England medical Center.
72.
go back to reference Landgraf, J. M. (2007). Precision and sensitivity of the short-form pediatric enuresis module to assess quality of life (PEMQOL). Journal of Pediatric Urology, 3(2), 109–117.PubMedCrossRef Landgraf, J. M. (2007). Precision and sensitivity of the short-form pediatric enuresis module to assess quality of life (PEMQOL). Journal of Pediatric Urology, 3(2), 109–117.PubMedCrossRef
73.
go back to reference Walters, S. J. (2009). Quality of life outcomes in clinical trials and health-care evaluation: A practical guide to analysis and interpretation. Chichester, UK: Wiley. Walters, S. J. (2009). Quality of life outcomes in clinical trials and health-care evaluation: A practical guide to analysis and interpretation. Chichester, UK: Wiley.
74.
go back to reference Streiner, D. L., & Norman, G. R. (2008). Biostatistics: The bare essentials (3rd ed.). Shelton, Conn: People’s Medical Publication House. Streiner, D. L., & Norman, G. R. (2008). Biostatistics: The bare essentials (3rd ed.). Shelton, Conn: People’s Medical Publication House.
75.
go back to reference Gorsuch, R. L. (1983). Factor analysis (2nd ed.). Hillsdale, NJ: Lawrence Erlbaum. Gorsuch, R. L. (1983). Factor analysis (2nd ed.). Hillsdale, NJ: Lawrence Erlbaum.
76.
go back to reference Camfield, L. (2012). Quality of life in developing countries. In K. C. Land, A. C. Michalos, & S. Sirgy (Eds.), Handbook of social indicators and quality of life research (pp. 399–432). New York: Springer.CrossRef Camfield, L. (2012). Quality of life in developing countries. In K. C. Land, A. C. Michalos, & S. Sirgy (Eds.), Handbook of social indicators and quality of life research (pp. 399–432). New York: Springer.CrossRef
77.
go back to reference Myaskovsky, L., Burkitt, K. H., Lichy, A. M., et al. (2011). The association of race, cultural factors, and health-related quality of life in persons with spinal cord injury. Archives of Physical Medicine and Rehabilitation, 92(3), 441–448.PubMedCrossRef Myaskovsky, L., Burkitt, K. H., Lichy, A. M., et al. (2011). The association of race, cultural factors, and health-related quality of life in persons with spinal cord injury. Archives of Physical Medicine and Rehabilitation, 92(3), 441–448.PubMedCrossRef
78.
go back to reference Kuhlthau, K., Hill, K. S., Yucel, R., & Perrin, J. M. (2005). Financial burden for families of children with special health care needs. Maternal and Child Health Journal, 9(2), 207–218.PubMedCrossRef Kuhlthau, K., Hill, K. S., Yucel, R., & Perrin, J. M. (2005). Financial burden for families of children with special health care needs. Maternal and Child Health Journal, 9(2), 207–218.PubMedCrossRef
79.
go back to reference Busch, S. H., & Barry, C. L. (2007). Mental health disorders in childhood: assessing the burden on families. Health Affairs (Millwood), 26(4), 1088–1095.CrossRef Busch, S. H., & Barry, C. L. (2007). Mental health disorders in childhood: assessing the burden on families. Health Affairs (Millwood), 26(4), 1088–1095.CrossRef
80.
go back to reference Pawankar, R. A., Canonica, G. W., Holgate, S. T., et al. (2012). Allergic diseases and asthma: A major global health concern. Current opinion in Allergy and Clinical Immunology, 12(1), 39–41.PubMedCrossRef Pawankar, R. A., Canonica, G. W., Holgate, S. T., et al. (2012). Allergic diseases and asthma: A major global health concern. Current opinion in Allergy and Clinical Immunology, 12(1), 39–41.PubMedCrossRef
83.
go back to reference Polinder, S., Haagsma, J. A., Lyons, R. A., et al. (2012). Measuring the population burden of fatal and nonfatal injury. Epidemiologic Reviews, 34(1), 17–31.PubMedCrossRef Polinder, S., Haagsma, J. A., Lyons, R. A., et al. (2012). Measuring the population burden of fatal and nonfatal injury. Epidemiologic Reviews, 34(1), 17–31.PubMedCrossRef
84.
go back to reference Boland, D. F., & Stacy, M. (2012). The economic and quality of life burden associated with parkinson’s disease: a focus on symptoms. The American Journal of Managed Care, 18(7 Suppl), s168–s175.PubMed Boland, D. F., & Stacy, M. (2012). The economic and quality of life burden associated with parkinson’s disease: a focus on symptoms. The American Journal of Managed Care, 18(7 Suppl), s168–s175.PubMed
85.
go back to reference Pike, J., Jones, E., Rajagopalan, K., Piercy, J., & Anderson, P. (2012). Social and economic burden of walking and mobility problems in multiple sclerosis. BMC Neurol, 12(1), 94.PubMedCrossRef Pike, J., Jones, E., Rajagopalan, K., Piercy, J., & Anderson, P. (2012). Social and economic burden of walking and mobility problems in multiple sclerosis. BMC Neurol, 12(1), 94.PubMedCrossRef
86.
go back to reference Weitzner, M. A., Meyers, C. A., Steinbruecker, S., et al. (1997). Developing a care giver quality-of-life instrument. Preliminary steps. Cancer Practice, 5(1), 25–31.PubMed Weitzner, M. A., Meyers, C. A., Steinbruecker, S., et al. (1997). Developing a care giver quality-of-life instrument. Preliminary steps. Cancer Practice, 5(1), 25–31.PubMed
Metagegevens
Titel
Condition-specific quality of life questionnaires for caregivers of children with pediatric conditions: a systematic review
Auteurs
Maria Yui Kwan Chow
Angela M. Morrow
Spring Chenoa Cooper Robbins
Julie Leask
Publicatiedatum
01-10-2013
Uitgeverij
Springer Netherlands
Gepubliceerd in
Quality of Life Research / Uitgave 8/2013
Print ISSN: 0962-9343
Elektronisch ISSN: 1573-2649
DOI
https://doi.org/10.1007/s11136-012-0343-z

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