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Gepubliceerd in: Quality of Life Research 2/2012

01-03-2012

Development of the PedsQL™ sickle cell disease module items: qualitative methods

Auteurs: Julie A. Panepinto, Sylvia Torres, James W. Varni

Gepubliceerd in: Quality of Life Research | Uitgave 2/2012

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Abstract

Purpose

The objective of this qualitative study was to develop the items and support the content validity of the PedsQL™ Sickle Cell Disease Module for pediatric patients with sickle cell disease (SCD).

Methods

The iterative process included multiphase qualitative methodology. A literature review on SCD was conducted to generate domains of interest for the individual in-depth interviews. Ten healthcare experts with clinical experience in SCD participated in the development of the conceptual framework. A total of 13 pediatric patients with SCD ages 5–18 and 18 parents of patients ages 2–18 participated in the individual in-depth interviews. A total of 33 pediatric patients with SCD ages 5–18 and 39 parents of patients ages 2–18 participated in individually conducted cognitive interviews that included both think aloud and cognitive debriefing techniques to assess the interpretability and readability of the item stems.

Results

Six domains were derived from the qualitative methods involving patient/parent interviews and expert opinion, with content saturation achieved, resulting in 48 items. The six domains consisted of items measuring Pain Intensity/Location (9 items), Pain Interference (11 items), Worry (7 items), Emotions (3 items), Disease Symptoms/Treatment, (12 items), and Communication (6 items).

Conclusions

Qualitative methods involving pediatric patients and parents in the item development process support the content validity for the PedsQL™ SCD Module. The PedsQL™ SCD Module is now undergoing national multisite field testing for the psychometric validation phase of instrument development.
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1
The number of items might change as a function of the quantitative analyses.
 
Literatuur
1.
go back to reference Charache, S., Terrin, M. L., Moore, R. D., Dover, G. J., Barton, F. B., Eckert, S. V., et al. (1995). Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the multicenter study of hydroxyurea in sickle cell anemia. New England Journal of Medicine, 332, 1317–1322.PubMedCrossRef Charache, S., Terrin, M. L., Moore, R. D., Dover, G. J., Barton, F. B., Eckert, S. V., et al. (1995). Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the multicenter study of hydroxyurea in sickle cell anemia. New England Journal of Medicine, 332, 1317–1322.PubMedCrossRef
2.
go back to reference Platt, O. S., Brambilla, D. J., Rosse, W. F., Milner, P. F., Castro, O., Steinberg, M. H., et al. (1994). Mortality in sickle cell disease. Life expectancy and risk factors for early death. New England Journal of Medicine, 330, 1639–1644.PubMedCrossRef Platt, O. S., Brambilla, D. J., Rosse, W. F., Milner, P. F., Castro, O., Steinberg, M. H., et al. (1994). Mortality in sickle cell disease. Life expectancy and risk factors for early death. New England Journal of Medicine, 330, 1639–1644.PubMedCrossRef
3.
go back to reference Platt, O. S., Thorington, B. D., Brambilla, D. J., Milner, P. F., Rosse, W. F., Vichinsky, E., et al. (1991). Pain in sickle cell disease. Rates and risk factors. New England Journal of Medicine, 325, 11–16.PubMedCrossRef Platt, O. S., Thorington, B. D., Brambilla, D. J., Milner, P. F., Rosse, W. F., Vichinsky, E., et al. (1991). Pain in sickle cell disease. Rates and risk factors. New England Journal of Medicine, 325, 11–16.PubMedCrossRef
4.
go back to reference Dampier, C., Lieff, S., LeBeau, P., Rhee, S., McMurray, M., Rogers, Z., et al. (2010). Health-related quality of life in children with sickle cell disease: A report from the comprehensive sickle cell centers clinical trial consortium. Pediatric Blood & Cancer, 55, 485–494.CrossRef Dampier, C., Lieff, S., LeBeau, P., Rhee, S., McMurray, M., Rogers, Z., et al. (2010). Health-related quality of life in children with sickle cell disease: A report from the comprehensive sickle cell centers clinical trial consortium. Pediatric Blood & Cancer, 55, 485–494.CrossRef
5.
go back to reference Panepinto, J. A., O’Mahar, K. M., DeBaun, M. R., Rennie, K. M., & Scott, J. P. (2004). Validity of the Child Health Questionnaire for use in children with sickle cell disease. Journal of Pediatric Hematology/oncology, 26, 574–578.PubMedCrossRef Panepinto, J. A., O’Mahar, K. M., DeBaun, M. R., Rennie, K. M., & Scott, J. P. (2004). Validity of the Child Health Questionnaire for use in children with sickle cell disease. Journal of Pediatric Hematology/oncology, 26, 574–578.PubMedCrossRef
6.
go back to reference Panepinto, J. A., Pajewski, N. M., Foerster, L. M., & Hoffmann, R. G. (2008). The performance of the PedsQL™ Generic Core Scales in children with sickle cell disease. Journal of Pediatric Hematology/oncology, 30, 666–673.PubMedCrossRef Panepinto, J. A., Pajewski, N. M., Foerster, L. M., & Hoffmann, R. G. (2008). The performance of the PedsQL™ Generic Core Scales in children with sickle cell disease. Journal of Pediatric Hematology/oncology, 30, 666–673.PubMedCrossRef
7.
go back to reference Panepinto, J. A., O’Mahar, K. M., DeBaun, M. R., Loberiza, F. R., & Scott, J. P. (2005). Health-related quality of life in children with sickle cell disease: Child and parent perception. British Journal Haematology, 130, 437–444.CrossRef Panepinto, J. A., O’Mahar, K. M., DeBaun, M. R., Loberiza, F. R., & Scott, J. P. (2005). Health-related quality of life in children with sickle cell disease: Child and parent perception. British Journal Haematology, 130, 437–444.CrossRef
8.
go back to reference Varni, J. W., & Limbers, C. A. (2009). The Pediatric Quality of Life Inventory: Measuring pediatric health-related quality of life from the perspective of children and their parents. Pediatric Clinics of North America, 56, 843–863.PubMedCrossRef Varni, J. W., & Limbers, C. A. (2009). The Pediatric Quality of Life Inventory: Measuring pediatric health-related quality of life from the perspective of children and their parents. Pediatric Clinics of North America, 56, 843–863.PubMedCrossRef
9.
go back to reference Patrick, D. L., & Deyo, R. A. (1989). Generic and disease-specific measures in assessing health status and quality of life. Medical Care, 27, S217–S233.PubMedCrossRef Patrick, D. L., & Deyo, R. A. (1989). Generic and disease-specific measures in assessing health status and quality of life. Medical Care, 27, S217–S233.PubMedCrossRef
10.
go back to reference Lasch, K. E., Marquis, P., Vigneux, M., Abetz, L., Arnould, B., Bayliss, M., et al. (2010). Pro development: Rigorous qualitative research as the crucial foundation. Quality of Life Research, 19, 1087–1096.PubMedCrossRef Lasch, K. E., Marquis, P., Vigneux, M., Abetz, L., Arnould, B., Bayliss, M., et al. (2010). Pro development: Rigorous qualitative research as the crucial foundation. Quality of Life Research, 19, 1087–1096.PubMedCrossRef
11.
go back to reference Irwin, D. E., Varni, J. W., Yeatts, K., & DeWalt, D. A. (2009). Cognitive interviewing methodology in the development of a pediatric item bank: A patient reported outcomes measurement information system (PROMIS) study. Health and Quality of Life Outcomes, 7(3), 1–10. Irwin, D. E., Varni, J. W., Yeatts, K., & DeWalt, D. A. (2009). Cognitive interviewing methodology in the development of a pediatric item bank: A patient reported outcomes measurement information system (PROMIS) study. Health and Quality of Life Outcomes, 7(3), 1–10.
12.
go back to reference Varni, J. W., Burwinkle, T. M., Berrin, S. J., Sherman, S. A., Artavia, K., Malcarne, V. L., et al. (2006). The PedsQL™ in pediatric cerebral palsy: Reliability, validity, and sensitivity of the generic core scales and cerebral palsy module. Developmental Medicine and Child Neurology, 48, 442–449.PubMedCrossRef Varni, J. W., Burwinkle, T. M., Berrin, S. J., Sherman, S. A., Artavia, K., Malcarne, V. L., et al. (2006). The PedsQL™ in pediatric cerebral palsy: Reliability, validity, and sensitivity of the generic core scales and cerebral palsy module. Developmental Medicine and Child Neurology, 48, 442–449.PubMedCrossRef
13.
go back to reference Varni, J. W., Burwinkle, T. M., Jacobs, J. R., Gottschalk, M., Kaufman, F., & Jones, K. L. (2003). The PedsQL™ in type 1 and type 2 diabetes: Reliability and validity of the Pediatric Quality of Life Inventory™ Generic Core Scales and type 1 diabetes module. Diabetes Care, 26, 631–637.PubMedCrossRef Varni, J. W., Burwinkle, T. M., Jacobs, J. R., Gottschalk, M., Kaufman, F., & Jones, K. L. (2003). The PedsQL™ in type 1 and type 2 diabetes: Reliability and validity of the Pediatric Quality of Life Inventory™ Generic Core Scales and type 1 diabetes module. Diabetes Care, 26, 631–637.PubMedCrossRef
14.
go back to reference Varni, J. W., Burwinkle, T. M., Katz, E. R., Meeske, K., & Dickinson, P. (2002). The PedsQL™ in pediatric cancer: Reliability and validity of the Pediatric Quality of Life Inventory™ Generic Core Scales, Multidimensional Fatigue Scale, and Cancer Module. Cancer, 94, 2090–2106.PubMedCrossRef Varni, J. W., Burwinkle, T. M., Katz, E. R., Meeske, K., & Dickinson, P. (2002). The PedsQL™ in pediatric cancer: Reliability and validity of the Pediatric Quality of Life Inventory™ Generic Core Scales, Multidimensional Fatigue Scale, and Cancer Module. Cancer, 94, 2090–2106.PubMedCrossRef
15.
go back to reference Varni, J. W., Burwinkle, T. M., Rapoff, M. A., Kamps, J. L., & Olson, N. (2004). The PedsQL™ in pediatric asthma: Reliability and validity of the Pediatric Quality of Life Inventory™ Generic Core Scales and Asthma Module. Journal of Behavioral Medicine, 27, 297–318.PubMedCrossRef Varni, J. W., Burwinkle, T. M., Rapoff, M. A., Kamps, J. L., & Olson, N. (2004). The PedsQL™ in pediatric asthma: Reliability and validity of the Pediatric Quality of Life Inventory™ Generic Core Scales and Asthma Module. Journal of Behavioral Medicine, 27, 297–318.PubMedCrossRef
16.
go back to reference Varni, J. W., Seid, M., Knight, T. S., Burwinkle, T. M., Brown, J., & Szer, I. S. (2002). The PedsQL™ in pediatric rheumatology: Reliability, validity, and responsiveness of the Pediatric Quality of Life Inventory™ Generic Core Scales and Rheumatology Module. Arthritis and Rheumatism, 46, 714–725.PubMedCrossRef Varni, J. W., Seid, M., Knight, T. S., Burwinkle, T. M., Brown, J., & Szer, I. S. (2002). The PedsQL™ in pediatric rheumatology: Reliability, validity, and responsiveness of the Pediatric Quality of Life Inventory™ Generic Core Scales and Rheumatology Module. Arthritis and Rheumatism, 46, 714–725.PubMedCrossRef
17.
go back to reference Goldstein, S. L., Graham, N., Warady, B. A., Seikaly, M., McDonald, R., Burwinkle, T. M., et al. (2008). Measuring health-related quality of life in children with ESRD: Performance of the Generic and ESRD-Specific Instrument of the Pediatric Quality of Life Inventory™ (PedsQL™). American Journal of Kidney Diseases, 51, 285–297.PubMedCrossRef Goldstein, S. L., Graham, N., Warady, B. A., Seikaly, M., McDonald, R., Burwinkle, T. M., et al. (2008). Measuring health-related quality of life in children with ESRD: Performance of the Generic and ESRD-Specific Instrument of the Pediatric Quality of Life Inventory™ (PedsQL™). American Journal of Kidney Diseases, 51, 285–297.PubMedCrossRef
18.
go back to reference Palmer, S. N., Meeske, K. A., Katz, E. R., Burwinkle, T. M., & Varni, J. W. (2007). The PedsQL™ Brain Tumor Module: Initial reliability and validity. Pediatric Blood & Cancer, 49, 287–293.CrossRef Palmer, S. N., Meeske, K. A., Katz, E. R., Burwinkle, T. M., & Varni, J. W. (2007). The PedsQL™ Brain Tumor Module: Initial reliability and validity. Pediatric Blood & Cancer, 49, 287–293.CrossRef
19.
go back to reference Weissberg-Benchell, J., Zielinski, T. E., Rodgers, S., Greenley, R. N., Askenazi, D., Goldstein, S. L., et al. (2010). Pediatric health-related quality of life: Feasibility, reliability and validity of the PedsQL™ Transplant Module. American Journal of Transplantation, 10, 1677–1685.PubMedCrossRef Weissberg-Benchell, J., Zielinski, T. E., Rodgers, S., Greenley, R. N., Askenazi, D., Goldstein, S. L., et al. (2010). Pediatric health-related quality of life: Feasibility, reliability and validity of the PedsQL™ Transplant Module. American Journal of Transplantation, 10, 1677–1685.PubMedCrossRef
20.
go back to reference DA, F. (2009). Guidance for industry: Patient-reported outcome measures: Use in medical product development to support labeling claims. Rockville, MD: Food and Drug Administration, US Department of Health and Human Services. DA, F. (2009). Guidance for industry: Patient-reported outcome measures: Use in medical product development to support labeling claims. Rockville, MD: Food and Drug Administration, US Department of Health and Human Services.
21.
go back to reference Lasch, K. E., Marquis, P., Vigneux, M., Abetz, L., Arnould, B., Bayliss, M., et al. (2010). Pro development: Rigorous qualitative research as the crucial foundation. Quality of Life Research, 19, 1087–1096.PubMedCrossRef Lasch, K. E., Marquis, P., Vigneux, M., Abetz, L., Arnould, B., Bayliss, M., et al. (2010). Pro development: Rigorous qualitative research as the crucial foundation. Quality of Life Research, 19, 1087–1096.PubMedCrossRef
22.
go back to reference Brod, M., Tesler, L. E., & Christensen, T. L. (2009). Qualitative research and content validity: Developing best practices based on science and experience. Quality of Life Research, 18, 1263–1278.PubMedCrossRef Brod, M., Tesler, L. E., & Christensen, T. L. (2009). Qualitative research and content validity: Developing best practices based on science and experience. Quality of Life Research, 18, 1263–1278.PubMedCrossRef
23.
go back to reference Krueger, R. A., & Casey, M. A. (2000). Focus groups: A practical guide for applied research (3rd ed.). Thousand Oaks, CA: Sage Publications. Krueger, R. A., & Casey, M. A. (2000). Focus groups: A practical guide for applied research (3rd ed.). Thousand Oaks, CA: Sage Publications.
25.
go back to reference Irwin, D. E., Stucky, B. D., Thissen, D., DeWitt, E. M., Lai, J. S., Yeatts, K., et al. (2010). Sampling plan and patient characteristics of the promis pediatrics large-scale survey. Quality of Life Research, 19, 585–594.PubMedCrossRef Irwin, D. E., Stucky, B. D., Thissen, D., DeWitt, E. M., Lai, J. S., Yeatts, K., et al. (2010). Sampling plan and patient characteristics of the promis pediatrics large-scale survey. Quality of Life Research, 19, 585–594.PubMedCrossRef
26.
go back to reference Varni, J. W., Stucky, B. D., Thissen, D., DeWitt, E. M., Irwin, D. E., Lai, J. S., et al. (2010). PROMIS pediatric pain interference scale: An item response theory analysis of the pediatric pain item bank. Journal of Pain, 11, 1109–1119.PubMedCrossRef Varni, J. W., Stucky, B. D., Thissen, D., DeWitt, E. M., Irwin, D. E., Lai, J. S., et al. (2010). PROMIS pediatric pain interference scale: An item response theory analysis of the pediatric pain item bank. Journal of Pain, 11, 1109–1119.PubMedCrossRef
27.
go back to reference Irwin, D. E., Stucky, B. D., Langer, M. M., Thissen, D., DeWitt, E. M., Lai, J. S., et al. (2010). An item response analysis of the pediatric PROMIS anxiety and depressive symptoms scales. Quality of Life Research, 19, 595–607.PubMedCrossRef Irwin, D. E., Stucky, B. D., Langer, M. M., Thissen, D., DeWitt, E. M., Lai, J. S., et al. (2010). An item response analysis of the pediatric PROMIS anxiety and depressive symptoms scales. Quality of Life Research, 19, 595–607.PubMedCrossRef
28.
go back to reference Yeatts, K., Stucky, B. D., Thissen, D., Irwin, D. E., Varni, J. W., DeWitt, E. M., et al. (2010). Construction of the pediatric asthma impact scale (PAIS) for the patient-reported outcomes measurement information system (PROMIS). Journal of Asthma, 47, 295–302.PubMedCrossRef Yeatts, K., Stucky, B. D., Thissen, D., Irwin, D. E., Varni, J. W., DeWitt, E. M., et al. (2010). Construction of the pediatric asthma impact scale (PAIS) for the patient-reported outcomes measurement information system (PROMIS). Journal of Asthma, 47, 295–302.PubMedCrossRef
29.
go back to reference Marcus, S. B., Strople, J. A., Neighbors, K., Weissberg-Benchell, J., Nelson, S. P., Limbers, C. A., et al. (2009). Fatigue and health-related quality of life in pediatric inflammatory bowel disease. Clinical Gastroenterology and Hepatology, 7, 554–561.PubMedCrossRef Marcus, S. B., Strople, J. A., Neighbors, K., Weissberg-Benchell, J., Nelson, S. P., Limbers, C. A., et al. (2009). Fatigue and health-related quality of life in pediatric inflammatory bowel disease. Clinical Gastroenterology and Hepatology, 7, 554–561.PubMedCrossRef
30.
go back to reference Varni, J. W., Limbers, C. A., Bryant, W. P., & Wilson, D. P. (2009). The PedsQL™ Multidimensional Fatigue Scale in type 1 diabetes: Feasibility, reliability, and validity. Pediatric Diabetes, 10, 321–328.PubMedCrossRef Varni, J. W., Limbers, C. A., Bryant, W. P., & Wilson, D. P. (2009). The PedsQL™ Multidimensional Fatigue Scale in type 1 diabetes: Feasibility, reliability, and validity. Pediatric Diabetes, 10, 321–328.PubMedCrossRef
31.
go back to reference Varni, J. W., Limbers, C. A., Bryant, W. P., & Wilson, D. P. (2010). The PedsQL™ Multidimensional Fatigue Scale in pediatric obesity: Feasibility, reliability, and validity. International Journal of Pediatric Obesity, 5, 34–42.PubMedCrossRef Varni, J. W., Limbers, C. A., Bryant, W. P., & Wilson, D. P. (2010). The PedsQL™ Multidimensional Fatigue Scale in pediatric obesity: Feasibility, reliability, and validity. International Journal of Pediatric Obesity, 5, 34–42.PubMedCrossRef
32.
go back to reference Gold, J. I., Mahrer, N. E., Yee, J., & Palermo, T. M. (2009). Pain, fatigue, and health-related quality of life in children and adolescents with chronic pain. Clinical Journal of Pain, 25, 407–412.PubMedCrossRef Gold, J. I., Mahrer, N. E., Yee, J., & Palermo, T. M. (2009). Pain, fatigue, and health-related quality of life in children and adolescents with chronic pain. Clinical Journal of Pain, 25, 407–412.PubMedCrossRef
33.
go back to reference Varni, J. W., Burwinkle, T. M., Limbers, C. A., & Szer, I. S. (2007). The PedsQL™ as a patient-reported outcome in children and adolescents with fibromyalgia: An analysis of OMERACT domains. Health and Quality of Life Outcomes, 5(9), 1–12.PubMedCrossRef Varni, J. W., Burwinkle, T. M., Limbers, C. A., & Szer, I. S. (2007). The PedsQL™ as a patient-reported outcome in children and adolescents with fibromyalgia: An analysis of OMERACT domains. Health and Quality of Life Outcomes, 5(9), 1–12.PubMedCrossRef
34.
go back to reference Varni, J. W., Burwinkle, T. M., & Szer, I. S. (2004). The PedsQL™ Multidimensional Fatigue Scale in pediatric rheumatology: Reliability and validity. Journal of Rheumatology, 31, 2494–2500.PubMed Varni, J. W., Burwinkle, T. M., & Szer, I. S. (2004). The PedsQL™ Multidimensional Fatigue Scale in pediatric rheumatology: Reliability and validity. Journal of Rheumatology, 31, 2494–2500.PubMed
35.
go back to reference Guest, G., Bunce, A., & Johnson, L. (2006). How many interviews are enough? An experiment with data saturation and variability. Field Methods, 18, 59–82.CrossRef Guest, G., Bunce, A., & Johnson, L. (2006). How many interviews are enough? An experiment with data saturation and variability. Field Methods, 18, 59–82.CrossRef
Metagegevens
Titel
Development of the PedsQL™ sickle cell disease module items: qualitative methods
Auteurs
Julie A. Panepinto
Sylvia Torres
James W. Varni
Publicatiedatum
01-03-2012
Uitgeverij
Springer Netherlands
Gepubliceerd in
Quality of Life Research / Uitgave 2/2012
Print ISSN: 0962-9343
Elektronisch ISSN: 1573-2649
DOI
https://doi.org/10.1007/s11136-011-9941-4

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