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Published in: Journal of Clinical Psychology in Medical Settings 2/2020

01-06-2020 | Mood Disorders

Systematic Review: Pain and Emotional Functioning in Pediatric Sickle Cell Disease

Authors: Steven K. Reader, Laura M. Rockman, Katherine M. Okonak, Nicole M. Ruppe, Colleen N. Keeler, Anne E. Kazak

Published in: Journal of Clinical Psychology in Medical Settings | Issue 2/2020

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Abstract

The objective of this systematic review was to assess the relationship between pain (frequency/intensity/duration, impairment, coping) and emotional functioning in pediatric Sickle Cell Disease, and evaluate the state of the literature. Studies were included if they met each of the following criteria: (a) primarily pediatric sample of youth or young adults up to age 21 years with SCD, (b) examined emotional functioning including anxiety and/or depressive and/or internalizing symptoms, and/or affect, (c) examined pain intensity/frequency/duration and/or pain-related impairment and/or pain coping as it relates to emotional functioning, as defined above. Using the established guidelines for systematic reviews, we searched PsycINFO, PubMED, and CINAHL databases for studies published through June 2018. Screening resulted in 33 studies meeting inclusion criteria. Study data were extracted and evaluated for scientific merit, resulting in four studies being removed. 29 studies were included in the final synthesis. Studies provide strongest evidence of a relationship between increased pain frequency and higher depressive and anxiety symptoms. There are moderate-to-strong associations between pain-related impairment and depressive symptoms, and small-to-strong associations between pain-related impairment and anxiety. When examining pain-coping strategies, maladaptive cognitive strategies show the strongest association with emotional functioning. There is a need for more adequately powered, prospective studies based on theoretical frameworks in order to advance our understanding of the relationship between pain and emotional functioning in pediatric SCD.
Literature
go back to reference Bakshi, N., Lukombo, I., Belfer, I., & Krishnamurti, L. (2018). Pain catastrophizing is associated with poorer health-related quality of life in pediatric patients with sickle cell disease. Journal of Pain Research,11, 947–953.CrossRef Bakshi, N., Lukombo, I., Belfer, I., & Krishnamurti, L. (2018). Pain catastrophizing is associated with poorer health-related quality of life in pediatric patients with sickle cell disease. Journal of Pain Research,11, 947–953.CrossRef
go back to reference Bakshi, N., Lukombo, I., Shnol, H., Belfer, I., & Krishnamurti, L. (2017). Psychological characteristics and pain frequency are associated with experimental pain sensitivity in pediatric patients with sickle cell disease. The Journal of Pain,18, 1216–1228.CrossRef Bakshi, N., Lukombo, I., Shnol, H., Belfer, I., & Krishnamurti, L. (2017). Psychological characteristics and pain frequency are associated with experimental pain sensitivity in pediatric patients with sickle cell disease. The Journal of Pain,18, 1216–1228.CrossRef
go back to reference Barakat, L. P., Patterson, C. A., Daniel, L. C., & Dampier, C. (2008). Quality of life among adolescents with sickle cell disease: Mediation of pain by internalizing symptoms and parenting stress. Health and Quality of Life Outcomes,6, 1–9.CrossRef Barakat, L. P., Patterson, C. A., Daniel, L. C., & Dampier, C. (2008). Quality of life among adolescents with sickle cell disease: Mediation of pain by internalizing symptoms and parenting stress. Health and Quality of Life Outcomes,6, 1–9.CrossRef
go back to reference Bennett, D. S. (1994). Depression among children with chronic medical problems: A meta-analysis. Journal of Pediatric Psychology,19, 149–169.CrossRef Bennett, D. S. (1994). Depression among children with chronic medical problems: A meta-analysis. Journal of Pediatric Psychology,19, 149–169.CrossRef
go back to reference Benton, T. D., Ifeagwu, J. A., & Smith-Whitley, K. (2007). Anxiety and depression in children and adolescents with sickle cell disease. Current Psychiatry Reports,9, 114–121.CrossRef Benton, T. D., Ifeagwu, J. A., & Smith-Whitley, K. (2007). Anxiety and depression in children and adolescents with sickle cell disease. Current Psychiatry Reports,9, 114–121.CrossRef
go back to reference Burlew, K., Telfair, J., Colangelo, L., & Wright, E. C. (2000). Factors that influence adolescent adaptation to sickle cell disease. Journal of Pediatric Psychology,25, 287–299.CrossRef Burlew, K., Telfair, J., Colangelo, L., & Wright, E. C. (2000). Factors that influence adolescent adaptation to sickle cell disease. Journal of Pediatric Psychology,25, 287–299.CrossRef
go back to reference Cartwright-Hatton, S., McNicol, K., & Doubleday, E. (2006). Anxiety in a neglected population: Prevalence of anxiety disorders in pre-adolescent children. Clinical Psychology Review,26, 817–833.CrossRef Cartwright-Hatton, S., McNicol, K., & Doubleday, E. (2006). Anxiety in a neglected population: Prevalence of anxiety disorders in pre-adolescent children. Clinical Psychology Review,26, 817–833.CrossRef
go back to reference Casey, R., Brown, R. T., & Bakeman, R. (2000). Predicting adjustment in children and adolescents with Sickle Cell Disease: A test of the Risk-Resistance-Adaptation model. Rehabilitation Psychology,45, 155–178.CrossRef Casey, R., Brown, R. T., & Bakeman, R. (2000). Predicting adjustment in children and adolescents with Sickle Cell Disease: A test of the Risk-Resistance-Adaptation model. Rehabilitation Psychology,45, 155–178.CrossRef
go back to reference Cohen, J. (1988). Statistical power analysis for the behavioral sciences (2nd ed.). Hillsdale, NJ: Lawrence Erlbaum Associates. Cohen, J. (1988). Statistical power analysis for the behavioral sciences (2nd ed.). Hillsdale, NJ: Lawrence Erlbaum Associates.
go back to reference Eiser, C. (1990). Psychological effects of chronic disease. Journal of Child Psychology and Psychiatry,31, 85–98.CrossRef Eiser, C. (1990). Psychological effects of chronic disease. Journal of Child Psychology and Psychiatry,31, 85–98.CrossRef
go back to reference Gil, K. M., Carson, J. W., Porter, L. S., Ready, J., Valrie, C., Redding-Lallinger, R., & Daeschner, C. (2003). Daily stress and mood and their association with pain, health-care use, and school activity in adolescents with sickle cell disease. Journal of Pediatric Psychology,28, 363–373. https://doi.org/10.1093/jpepsy/jsg026.CrossRefPubMed Gil, K. M., Carson, J. W., Porter, L. S., Ready, J., Valrie, C., Redding-Lallinger, R., & Daeschner, C. (2003). Daily stress and mood and their association with pain, health-care use, and school activity in adolescents with sickle cell disease. Journal of Pediatric Psychology,28, 363–373. https://​doi.​org/​10.​1093/​jpepsy/​jsg026.CrossRefPubMed
go back to reference Gil, K. M., Edens, J. L., Wilson, J. J., Raezer, L. B., Kinney, T. R., Schultz, W. H., & Daeschner, C. (1997). Coping strategies and laboratory pain in children with sickle cell disease. Annals of Behavioral Medicine,19, 22–29.CrossRef Gil, K. M., Edens, J. L., Wilson, J. J., Raezer, L. B., Kinney, T. R., Schultz, W. H., & Daeschner, C. (1997). Coping strategies and laboratory pain in children with sickle cell disease. Annals of Behavioral Medicine,19, 22–29.CrossRef
go back to reference Gil, K. M., Williams, D. A., Thompson, R. J., & Kinney, T. R. (1991). Sickle cell disease in children and adolescents: The relation of child and parent pain coping strategies to adjustment. Journal of Pediatric Psychology,16, 643–663.CrossRef Gil, K. M., Williams, D. A., Thompson, R. J., & Kinney, T. R. (1991). Sickle cell disease in children and adolescents: The relation of child and parent pain coping strategies to adjustment. Journal of Pediatric Psychology,16, 643–663.CrossRef
go back to reference Graumlich, S. E., Powers, S. W., Byars, K. C., Schwarber, L. A., Mitchell, M. J., & Kalinyak, K. A. (2001). Multidimensional assessment of pain in pediatric sickle cell disease. Journal of Pediatric Psychology,26, 203–214.CrossRef Graumlich, S. E., Powers, S. W., Byars, K. C., Schwarber, L. A., Mitchell, M. J., & Kalinyak, K. A. (2001). Multidimensional assessment of pain in pediatric sickle cell disease. Journal of Pediatric Psychology,26, 203–214.CrossRef
go back to reference Graves, J. K., Hodge, C., & Jacob, E. (2016). Depression, anxiety, and quality of life in children and adolescents with sickle cell disease. Pediatric Nursing,42, 113.PubMed Graves, J. K., Hodge, C., & Jacob, E. (2016). Depression, anxiety, and quality of life in children and adolescents with sickle cell disease. Pediatric Nursing,42, 113.PubMed
go back to reference Hassell, K. L. (2010). Population estimates of sickle cell disease in the U.S. American Journal of Preventative Medicine,38, S512–S521.CrossRef Hassell, K. L. (2010). Population estimates of sickle cell disease in the U.S. American Journal of Preventative Medicine,38, S512–S521.CrossRef
go back to reference Lemanek, K. L., Hahn, A., & McNaull, M. (2017). Sickle cell disease. In M. C. Roberts & R. G. Steele (Eds.), Handbook of pediatric psychology (pp. 269–283). New York: Guilford Press. Lemanek, K. L., Hahn, A., & McNaull, M. (2017). Sickle cell disease. In M. C. Roberts & R. G. Steele (Eds.), Handbook of pediatric psychology (pp. 269–283). New York: Guilford Press.
go back to reference Merikangas, K.R., He, J., Burstein, M., Swanson, S.A., Avenevoli, S., Cui, L., … Swendsen, J. (2010). Lifetime prevalence of mental disorders in U.S. adolescents: Results from the National Comorbidity Survey Replication—Adolescent Supplement. Journal of the American Academy of Child and Adolescent Psychiatry, 49, 980–989. Merikangas, K.R., He, J., Burstein, M., Swanson, S.A., Avenevoli, S., Cui, L., … Swendsen, J. (2010). Lifetime prevalence of mental disorders in U.S. adolescents: Results from the National Comorbidity Survey Replication—Adolescent Supplement. Journal of the American Academy of Child and Adolescent Psychiatry, 49, 980–989.
go back to reference Morgan, G. A., Gliner, J. A., & Harmon, R. J. (1999). Quantitative research approaches. Journal of the American Academy of Child and Adolescent Psychiatry,38, 1595–1597.CrossRef Morgan, G. A., Gliner, J. A., & Harmon, R. J. (1999). Quantitative research approaches. Journal of the American Academy of Child and Adolescent Psychiatry,38, 1595–1597.CrossRef
go back to reference Neale, J., & Liebert, R. (1986). Science and behavior: An introduction to methods of research. Englewood Cliffs, NJ: Prentice-Hall. Neale, J., & Liebert, R. (1986). Science and behavior: An introduction to methods of research. Englewood Cliffs, NJ: Prentice-Hall.
go back to reference Noll, R. B., Vannatta, K., Koontz, K., Kalinyak, K., Bukowski, W. M., & Davis, W. H. (1996). Peer relationships and emotional well-being of youngsters with sickle cell disease. Child Development,67, 423–436.PubMed Noll, R. B., Vannatta, K., Koontz, K., Kalinyak, K., Bukowski, W. M., & Davis, W. H. (1996). Peer relationships and emotional well-being of youngsters with sickle cell disease. Child Development,67, 423–436.PubMed
go back to reference Palermo, T. M. (2013). New guidelines for publishing review articles in JPP: Systematic reviews and topical reviews. Journal of Pediatric Psychology,38, 5–9.CrossRef Palermo, T. M. (2013). New guidelines for publishing review articles in JPP: Systematic reviews and topical reviews. Journal of Pediatric Psychology,38, 5–9.CrossRef
go back to reference Palermo, T. M., Valrie, C. R., & Karlson, C. W. (2014). Family and parent influences on pediatric chronic pain: A developmental perspective. American Psychologist,69, 142–152.CrossRef Palermo, T. M., Valrie, C. R., & Karlson, C. W. (2014). Family and parent influences on pediatric chronic pain: A developmental perspective. American Psychologist,69, 142–152.CrossRef
go back to reference Panepinto, J. A., & Bonner, M. (2012). Health-related quality of life in Sickle Cell Disease: Past, present, and future. Pediatric Blood & Cancer,59, 377–385.CrossRef Panepinto, J. A., & Bonner, M. (2012). Health-related quality of life in Sickle Cell Disease: Past, present, and future. Pediatric Blood & Cancer,59, 377–385.CrossRef
go back to reference Peterson, C. C., Palermo, T. M., Swift, E., Beebe, A., & Drotar, D. (2005). Assessment of psychoeducational needs in a clinical sample of children with sickle cell disease. Children’s Health Care,34, 133–148.CrossRef Peterson, C. C., Palermo, T. M., Swift, E., Beebe, A., & Drotar, D. (2005). Assessment of psychoeducational needs in a clinical sample of children with sickle cell disease. Children’s Health Care,34, 133–148.CrossRef
go back to reference Pillai Riddell, R., Racine, N., Craig, K. D., & Campbell, L. (2013). Psychological theories and biopsychosocial models in paediatric pain. In P. J. McGrath, et al. (Eds.), Oxford textbook of paediatric pain (pp. 85–94). Oxford: Oxford University Press.CrossRef Pillai Riddell, R., Racine, N., Craig, K. D., & Campbell, L. (2013). Psychological theories and biopsychosocial models in paediatric pain. In P. J. McGrath, et al. (Eds.), Oxford textbook of paediatric pain (pp. 85–94). Oxford: Oxford University Press.CrossRef
go back to reference Thompson, R. J., Gil, K. M., Burbach, D. J., Keith, B. R., & Kinney, T. R. (1993). Role of child and maternal processes in the psychological adjustment of children with sickle cell disease. Journal of Consulting and Clinical Psychology,61, 468–474.CrossRef Thompson, R. J., Gil, K. M., Burbach, D. J., Keith, B. R., & Kinney, T. R. (1993). Role of child and maternal processes in the psychological adjustment of children with sickle cell disease. Journal of Consulting and Clinical Psychology,61, 468–474.CrossRef
go back to reference Thompson, R. J., Gil, K. M., Keith, B. R., Gustafson, K. E., George, L. K., & Kinney, T. R. (1994). Psychological adjustment of children with sickle cell disease: Stability and change over a 10-month period. Journal of Consulting and Clinical Psychology,62, 856–860.CrossRef Thompson, R. J., Gil, K. M., Keith, B. R., Gustafson, K. E., George, L. K., & Kinney, T. R. (1994). Psychological adjustment of children with sickle cell disease: Stability and change over a 10-month period. Journal of Consulting and Clinical Psychology,62, 856–860.CrossRef
go back to reference Unal, S., Toros, F., Kutuk, M. O., & Uyaniker, M. G. (2011). Evaluation of the psychological problems of children with sickle cell anemia and their families. Pediatric Hematology and Oncology,28, 321–328.CrossRef Unal, S., Toros, F., Kutuk, M. O., & Uyaniker, M. G. (2011). Evaluation of the psychological problems of children with sickle cell anemia and their families. Pediatric Hematology and Oncology,28, 321–328.CrossRef
go back to reference Wagner, J. L., Connelly, M., Brown, R. T., Taylor, L. C., Rittle, C., & Wall-Cloues, B. (2004). Predictors of social anxiety in children and adolescents with sickle cell disease. Journal of Clinical Psychology in Medical Setting,11, 243–252.CrossRef Wagner, J. L., Connelly, M., Brown, R. T., Taylor, L. C., Rittle, C., & Wall-Cloues, B. (2004). Predictors of social anxiety in children and adolescents with sickle cell disease. Journal of Clinical Psychology in Medical Setting,11, 243–252.CrossRef
go back to reference Walco, G. A., & Dampier, C. D. (1990). Pain in children and adolescents with sickle cell disease: A descriptive study. Journal of Pediatric Psychology,15, 643–658.CrossRef Walco, G. A., & Dampier, C. D. (1990). Pain in children and adolescents with sickle cell disease: A descriptive study. Journal of Pediatric Psychology,15, 643–658.CrossRef
go back to reference Wallander, J. L., & Varni, J. W. (1992). Adjustment in children with chronic physical disorders: Programmatic research on a disability-stress-coping model. In A. M. La Greca, L. J. Siegel, J. L. Wallander, & C. E. Walker (Eds.), Advances in pediatric psychology. Stress and coping in child health (pp. 279–298). New York: Guilford Press. Wallander, J. L., & Varni, J. W. (1992). Adjustment in children with chronic physical disorders: Programmatic research on a disability-stress-coping model. In A. M. La Greca, L. J. Siegel, J. L. Wallander, & C. E. Walker (Eds.), Advances in pediatric psychology. Stress and coping in child health (pp. 279–298). New York: Guilford Press.
go back to reference Wallander, J., & Varni, J. W. (1998). Effects of pediatric chronic physical disorders on child and family adjustment. Journal of Child Psychology and Psychiatry,39, 29–46.CrossRef Wallander, J., & Varni, J. W. (1998). Effects of pediatric chronic physical disorders on child and family adjustment. Journal of Child Psychology and Psychiatry,39, 29–46.CrossRef
go back to reference Zempsky, W. T., Palermo, T. M., Corsi, J. M., Lewandowski, A. S., Zhou, C., & Casella, J. F. (2013). Daily changes in pain, mood and physical function in youth hospitalized for sickle cell disease pain. Pain Research & Management,18, 33–38.CrossRef Zempsky, W. T., Palermo, T. M., Corsi, J. M., Lewandowski, A. S., Zhou, C., & Casella, J. F. (2013). Daily changes in pain, mood and physical function in youth hospitalized for sickle cell disease pain. Pain Research & Management,18, 33–38.CrossRef
Metadata
Title
Systematic Review: Pain and Emotional Functioning in Pediatric Sickle Cell Disease
Authors
Steven K. Reader
Laura M. Rockman
Katherine M. Okonak
Nicole M. Ruppe
Colleen N. Keeler
Anne E. Kazak
Publication date
01-06-2020
Publisher
Springer US
Published in
Journal of Clinical Psychology in Medical Settings / Issue 2/2020
Print ISSN: 1068-9583
Electronic ISSN: 1573-3572
DOI
https://doi.org/10.1007/s10880-019-09647-x

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