Abstract
Youth living with chronic sickle cell disease (SCD) pain are at risk for psychosocial distress and high levels of pain catastrophizing that contribute to functional impairment. This study aimed to identify the unique long-term impact of pain catastrophizing on pain impairment among youth with SCD. Youth with chronic SCD pain (N = 63, 10–18 years old, 58.3% female, 95.1% Black or African American) were recruited within comprehensive SCD clinics and completed a battery of measures at baseline and 4-months follow-up. A linear hierarchical regression examined baseline demographic and clinical characteristics (child SCD genotype, age, and average pain intensity), psychosocial functioning (anxiety, depression), and pain catastrophizing as predictors of pain interference at 4-months follow-up. Pain catastrophizing was the only unique predictor of pain interference at 4-months follow-up. Among youth with chronic SCD pain, pain catastrophizing warrants greater consideration as an important predictor that influences pain management and overall functioning.
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Ader, D. N. (2007). Developing the patient-reported outcomes measurement information system (PROMIS).
Alberts, N. M., Badawy, S. M., Hodges, J., Estepp, J. H., Nwosu, C., Khan, H., et al. (2020). Development of the incharge health mobile app to improve adherence to hydroxyurea in patients with sickle cell disease: User-centered design approach. JMIR MHealth and UHealth, 8(5), e14884. https://doi.org/10.2196/14884
Asmundson, G. J., Noel, M., Petter, M., & Parkerson, H. A. (2012). Pediatric fear-avoidance model of chronic pain: Foundation, application and future directions. Pain Research & Management. https://doi.org/10.1155/2012/908061
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. https://doi.org/10.2147/JPR.S151198
Barakat, L. P., Schwartz, L. A., Simon, K., & Radcliffe, J. (2007). Negative thinking as a coping strategy mediator of pain and internalizing symptoms in adolescents with sickle cell disease. Journal of Behavioral Medicine, 30(3), 199–208. https://doi.org/10.1007/s10865-007-9103-x
Bonham, V. L. (2001). Race, ethnicity, and pain treatment: Striving to understand the causes and solutions to the disparities in pain treatment. Journal of Law, Medicine & Ethics, 29(1), 52–68. https://doi.org/10.1111/j.1748-720X.2001.tb00039.x
Brown, R. T., Connelly, M., Rittle, C., & Clouse, B. (2006). A longitudinal examination predicting emergency room use in children with sickle cell disease and their caregivers. Journal of Pediatric Psychology, 31(2), 163–173. https://doi.org/10.1093/jpepsy/jsj002
Burns, J. W., Kubilus, A., Bruehl, S., Harden, R. N., & Lofland, K. (2003). Do changes in cognitive factors influence outcome following multidisciplinary treatment for chronic pain? A cross-lagged panel analysis. Journal of Consulting and Clinical Psychology, 71(1), 81. https://doi.org/10.1037/0022-006X.71.1.81
Campbell, C. M., McCauley, L., Bounds, S. C., Mathur, V. A., Conn, L., Simango, M., & Fontaine, K. R. (2012). Changes in pain catastrophizing predict later changes in fibromyalgia clinical and experimental pain report: Cross-lagged panel analyses of dispositional and situational catastrophizing. Arthritis Research & Therapy, 14(5), 1–9. https://doi.org/10.1186/ar4073
Centers for Disease Control and Prevention. (2020c, December 14). What is sickle cell disease? https://www.cdc.gov/ncbddd/sicklecell/facts.html
Centers for Disease Control and Prevention. (2020b, December 16). Data & statistics on sickle cell disease. https://www.cdc.gov/ncbddd/sicklecell/data.html
Centers for Disease Control and Prevention. (2020a, December 16). Complications and treatment of sickle cell disease. https://www.cdc.gov/ncbddd/sicklecell/treatments.html
Cox, E. D., Connolly, J. R., Palta, M., Rajamanickam, V. P., & Flynn, K. E. (2020). Reliability and validity of PROMIS® pediatric family relationships short form in children 8–17 years of age with chronic disease. Quality of Life Research, 29(1), 191–199. https://doi.org/10.1007/s11136-019-02266-x
Crombez, G., Bijttebier, P., Eccleston, C., Mascagni, T., Mertens, G., Goubert, L., & Verstraeten, K. (2003). The child version of the pain catastrophizing scale (PCS-C): A preliminary validation. Pain, 104(3), 639–646. https://doi.org/10.1016/S0304-3959(03)00121-0
Crosby, L. E., Joffe, N. E., Irwin, M. K., Strong, H., Peugh, J., Shook, L., Kalinyak, K. A., & Mitchell, M. J. (2015). School performance and disease interference in adolescents with sickle cell disease. Physical Disabilities: Education and Related Services, 34(1), 14–30. https://doi.org/10.14434/pders.v34i1.13918
Dahlhamer, J., Lucas, J., Zelaya, C., Nahin, R., Mackey, S., DeBar, L., & Helmick, C. (2018). Prevalence of chronic pain and high-impact chronic pain among adults—United States, 2016. Morbidity and Mortality Weekly Report, 67(36), 1001. https://doi.org/10.15585/mmwr.mm6736a2
Dampier, C., Palermo, T. M., Darbari, D. S., Hassell, K., Smith, W., & Zempsky, W. (2017). AAPT diagnostic criteria for chronic sickle cell disease pain. The Journal of Pain, 18(5), 490–498. https://doi.org/10.1016/j.jpain.2016.12.016
Darnall, B. D., Sturgeon, J. A., Kao, M. C., Hah, J. M., & Mackey, S. C. (2014). From catastrophizing to recovery: A pilot study of a single-session treatment for pain catastrophizing. Journal of Pain Research, 7, 219. https://doi.org/10.2147/JPR.S62329
Donohoe, C., & Smith, E. L. (2019). Psychological predictors of pain in children and adolescents with sickle cell disease: A scoping review. Journal of Pediatric Oncology Nursing, 36(2), 150–159. https://doi.org/10.1177/1043454218819457
Driscoll, M. C. (2007). Sickle cell disease. Pediatrics in Review, 28(7), 259.
Farrar, J. T., Young, J. P., LaMoreaux, L., Werth, J. L., & Poole, R. M. (2001). Clinical importance of changes in chronic pain intensity measured on an 11-point numerical pain rating scale. Pain, 94(2), 149–158. https://doi.org/10.1016/S0304-3959(01)00349-9
Fingar, K.R, Owens, P. L., Reid, L. D., Mistry, K. B., & Barrett, M. L. (2019). Characteristics of inpatient hospital stays involving sickle cell disease, 2000–2016: Statistical Brief# 251.
Forsythe, L. P., Thorn, B., Day, M., & Shelby, G. (2011). Race and sex differences in primary appraisals, catastrophizing, and experimental pain outcomes. The Journal of Pain, 12(5), 563–572.
Gil, K. M., Thompson, R. J., Keith, B. R., Tota-Faucette, M., Noll, S., & Kinney, T. R. (1993). Sickle cell disease pain in children and adolescents: Change in pain frequency and coping strategies over time. Journal of Pediatric Psychology, 18(5), 621–637. https://doi.org/10.1093/jpepsy/18.5.621
Green, C. R., Anderson, K. O., Baker, T. A., Campbell, L. C., Decker, S., Fillingim, R. B., & Vallerand, A. H. (2003). The unequal burden of pain: Confronting racial and ethnic disparities in pain. Pain Medicine, 4(3), 277–294.
Hoffman, K. M., Trawalter, S., Axt, J. R., & Oliver, M. N. (2016). Racial bias in pain assessment and treatment recommendations, and false beliefs about biological differences between blacks and whites. Proceedings of the National Academy of Sciences, 113(16), 4296–4301.
Holroyd, K. A., Drew, J. B., Cottrell, C. K., Romanek, K. M., & Heh, V. (2007). Impaired functioning and quality of life in severe migraine: The role of catastrophizing and associated symptoms. Cephalalgia, 27(10), 1156–1165.
Huque, M. H., Carlin, J. B., Simpson, J. A., & Lee, K. J. (2018). A comparison of multiple imputation methods for missing data in longitudinal studies. BMC Medical Research Methodology, 18(1), 1–16. https://doi.org/10.1186/s12874-018-0615-6
Jastrowski Mano, K. E., Evans, J. R., Tran, S. T., Anderson Khan, K., Weisman, S. J., & Hainsworth, K. R. (2012). The psychometric properties of the screen for child anxiety related emotional disorders in pediatric chronic pain. Journal of Pediatric Psychology, 37(9), 999–1011. https://doi.org/10.1111/j.1468-2982.2007.01420.x
Kashikar-Zuck, S., Carle, A., Barnett, K., Goldschneider, K. R., Sherry, D. D., Mara, C. A., & DeWitt, E. M. (2016). Longitudinal evaluation of patient reported outcomes measurement information systems (PROMIS) measures in pediatric chronic pain. Pain, 157(2), 339. https://doi.org/10.1097/j.pain.0000000000000378
Kazak, A. E., Rourke, M. T., Alderfer, M. A., Pai, A., Reilly, A. F., & Meadows, A. T. (2007). Evidence-based assessment, intervention and psychosocial care in pediatric oncology: A blueprint for comprehensive services across treatment. Journal of Pediatric Psychology, 32(9), 1099–1110. https://doi.org/10.1093/jpepsy/jsm031
Lim, C. S., Karlson, C., Edmond, S. N., Welkom, J. S., Osunkwo, I., & Cohen, L. L. (2019). Emotion-focused avoidance coping mediates the association between pain and health-related quality of life in children with sickle cell disease. Journal of Pediatric Hematology/oncology, 41(3), 194–201. https://doi.org/10.1097/MPH.0000000000001429
Mann, C. M., Schanberg, L. E., Wang, M., von Scheven, E., Lucas, N., Hernandez, A., Ringold, S., & Reeve, B. B. (2020). Identifying clinically meaningful severity categories for PROMIS pediatric measures of anxiety, mobility, fatigue, and depressive symptoms in juvenile idiopathic arthritis and childhood-onset systemic lupus erythematosus. Quality of Life Research, 29(9), 2573–2584. https://doi.org/10.1007/s11136-020-02513-6
Martin, C. E., Johnson, E., Wechter, M. E., Leserman, J., & Zolnoun, D. A. (2011). Catastrophizing: A predictor of persistent pain among women with endometriosis at 1 year. Human Reproduction, 26(11), 3078–3084.
Meeus, M., Nijs, J., Van Mol, E., Truijen, S., & De Meirleir, K. (2012). Role of psychological aspects in both chronic pain and in daily functioning in chronic fatigue syndrome: A prospective longitudinal study. Clinical Rheumatology, 31(6), 921–929.
Meints, S. M., Wang, V., & Edwards, R. R. (2018). Sex and race differences in pain sensitization among patients with chronic low back pain. The Journal of Pain, 19(12), 1461–1470.
Miller, R., Coyne, E., Crowgey, E. L., Eckrich, D., Myers, J. C., Villanueva, R., et al. (2020). Implementation of a learning healthcare system for sickle cell disease. JAMIA Open, 3(3), 349–359. https://doi.org/10.1093/jamiaopen/ooaa024
Morgan, E. M., Mara, C. A., Huang, B., Barnett, K., Carle, A. C., Farrell, J. E., & Cook, K. F. (2017). Establishing clinical meaning and defining important differences for Patient-Reported Outcomes Measurement Information System (PROMIS((R))) measures in juvenile idiopathic arthritis using standard setting with patients, parents, and providers. Quality of Life Research, 26(3), 565–586. https://doi.org/10.1007/s11136-016-1468-2
Murray, C. B., Groenewald, C. B., de la Vega, R., & Palermo, T. M. (2020). Long-term impact of adolescent chronic pain on young adult educational, vocational, and social outcomes. Pain, 161(2), 439.
Myrvik, M. P., Brandow, A. M., Drendel, A. L., Yan, K., Hoffmann, R. G., & Panepinto, J. A. (2013). Clinically meaningful measurement of pain in children with sickle cell disease. Pediatric Blood & Cancer, 60(10), 1689–1695. https://doi.org/10.1002/pbc.24624
National Institutes of Health (NIH). (2002). National heart, lung, and blood institute division of blood diseases and resources. In National Institutes of Health (Ed.), The management of sickle cell disease (4th ed.). Bethesda, MD: Author.
Noel, M., Rabbitts, J. A., Tai, G. G., & Palermo, T. M. (2015). Remembering pain after surgery: A longitudinal examination of the role of pain catastrophizing in children’s and parents’ recall. Pain, 156(5), 800.
Palermo, T. M., Schwartz, L., Drotar, D., & McGowan, K. (2002). Parental report of health-related quality of life in children with sickle cell disease. Journal of Behavioral Medicine, 25(3), 269–283. https://doi.org/10.1023/A:1015332828213
Pielech, M., Ryan, M., Logan, D., Kaczynski, K., White, M. T., & Simons, L. E. (2014). Pain catastrophizing in children with chronic pain and their parents: Proposed clinical reference points and reexamination of the pain catastrophizing scale measure. Pain, 155(11), 2360–2367. https://doi.org/10.1016/j.pain.2014.08.035
Quartana, P. J., Campbell, C. M., & Edwards, R. R. (2009). Pain catastrophizing: A critical review. Expert Review of Neurotherapeutics, 9(5), 745–758. https://doi.org/10.1586/ern.09.34
Reader, S. K., Rockman, L. M., Okonak, K. M., Ruppe, N. M., Keeler, C. N., & Kazak, A. E. (2019). Systematic review: Pain and emotional functioning in pediatric sickle cell disease. Journal of Clinical Psychology in Medical Settings. https://doi.org/10.1007/s10880-019-09647-x
Reeve, B. B., Edwards, L. J., Jaeger, B. C., Hinds, P. S., Dampier, C., Gipson, D. S., & DeWalt, D. A. (2018). Assessing responsiveness over time of the PROMIS® pediatric symptom and function measures in cancer, nephrotic syndrome, and sickle cell disease. Quality of Life Research, 27(1), 249–257. https://doi.org/10.1007/s11136-017-1697-z
Rubin, D. B. (1987). Multiple imputation for survey nonresponse.
Schafer, J. (1997). Analysis of incomplete multivariate data. Chapman & Hall.
Sil, S., Cohen, L. L., & Dampier, C. (2016). Psychosocial and functional outcomes in youth with chronic sickle cell pain. The Clinical Journal of Pain, 32(6), 527–533. https://doi.org/10.1097/AJP.0000000000000289
Sil, S., Woodward, K. E., Johnson, Y. L., Dampier, C., & Cohen, L. L. (2021). Parental psychosocial distress in pediatric sickle cell disease and chronic pain. Journal of Pediatric Psychology. https://doi.org/10.1093/jpepsy/jsaa130
Singh, A. P., Haywood, C., Jr., Beach, M. C., Guidera, M., Lanzkron, S., Valenzuela-Araujo, D., & Dugas, A. F. (2016). Improving emergency providers’ attitudes toward sickle cell patients in pain. Journal of Pain and Symptom Management, 51(3), 628–632. https://doi.org/10.1016/j.jpainsymman.2015.11.004
Stone, A. L., Williams, Z., McNaull, M., Wilson, A. C., & Karlson, C. W. (2020). Daily associations between child and parent psychological factors and home opioid use in youth with sickle cell disease. Annals of Behavioral Medicine, 54(1), 61–66. https://doi.org/10.1093/abm/kaz022
Sullivan, M. J., Bishop, S. R., & Pivik, J. (1995). The pain catastrophizing scale: Development and validation. Psychological Assessment, 7(4), 524.
Sullivan, M. J. L., Martel, M. O., Tripp, D., Savard, A., & Crombez, G. (2006). The relation between catastrophizing and the communication of pain experience. Pain, 122(3), 282–288.
Sullivan, M. J., Thorn, B., Haythornthwaite, J. A., Keefe, F., Martin, M., Bradley, L. A., & Lefebvre, J. C. (2001). Theoretical perspectives on the relation between catastrophizing and pain. The Clinical Journal of Pain, 17(1), 52–64.
Tran, S. T., Jastrowski Mano, K. E., Hainsworth, K. R., Medrano, G. R., Anderson Khan, K., Weisman, S. J., & Davies, W. H. (2015). Distinct influences of anxiety and pain catastrophizing on functional outcomes in children and adolescents with chronic pain. Journal of Pediatric Psychology, 40(8), 744–755. https://doi.org/10.1093/jpepsy/jsv029
Turk, D. C., & Wilson, H. D. (2010). Fear of pain as a prognostic factor in chronic pain: Conceptual models, assessment, and treatment implications. Current Pain and Headache Reports, 14(2), 88–95. https://doi.org/10.1007/s11916-010-0094-x
Valrie, C., Floyd, A., Redding-Lallinger, R., & Fuh, B. (2020). Depression and anxiety as moderators of the pain-social functioning relationship in youth with sickle cell disease. Journal of Pain Research, 13, 729. https://doi.org/10.2147/JPR.S238115
Varni, J. W., Magnus, B., Stucky, B. D., Liu, Y., Quinn, H., Thissen, D., & DeWalt, D. A. (2014). Psychometric properties of the PROMIS® pediatric scales: Precision, stability, and comparison of different scoring and administration options. Quality of Life Research, 23(4), 1233–1243. https://doi.org/10.1007/s11136-013-0544-0
Varni, J. W., Stucky, B. D., Thissen, D., DeWitt, E. M., Irwin, D. E., Lai, J. S., & DeWalt, D. A. (2010). PROMIS pediatric pain interference scale: An item response theory analysis of the pediatric pain item bank. The Journal of Pain, 11(11), 1109–1119. https://doi.org/10.1016/j.jpain.2010.02.005
Vervoort, T., Goubert, L., Eccleston, C., Bijttebier, P., & Crombez, G. (2006). Catastrophic thinking about pain is independently associated with pain severity, disability, and somatic complaints in school children and children with chronic pain. Journal of Pediatric Psychology, 31(7), 674–683. https://doi.org/10.1093/jpepsy/jsj059
Wastnedge, E., Waters, D., Patel, S., Morrison, K., Goh, M. Y., Adeloye, D., & Rudan, I. (2018). The global burden of sickle cell disease in children under five years of age: A systematic review and meta-analysis. Journal of Global Health. https://doi.org/10.7189/jogh.08.021103
Welkom, J. S., Hwang, W. T., & Guite, J. W. (2013). Adolescent pain catastrophizing mediates the relationship between protective parental responses to pain and disability over time. Journal of Pediatric Psychology, 38(5), 541–550. https://doi.org/10.1093/jpepsy/jst011
Wertli, M. M., Burgstaller, J. M., Weiser, S., Steurer, J., Kofmehl, R., & Held, U. (2014). Influence of catastrophizing on treatment outcome in patients with nonspecific low back pain: A systematic review. Spine, 39(3), 263–273. https://doi.org/10.1097/BRS.0000000000000537
Westman, A. E., Boersma, K., Leppert, J., & Linton, S. J. (2011). Fear-avoidance beliefs, catastrophizing, and distress: A longitudinal subgroup analysis on patients with musculoskeletal pain. The Clinical Journal of Pain, 27(7), 567–577. https://doi.org/10.1097/ajp.0b013e318219ab6c
Zagustin, T. K. (2013). The role of cognitive behavioral therapy for chronic pain in adolescents. PM&R PM & R: THe Journal of Injury, Function, and Rehabilitation, 5(8), 697–704. https://doi.org/10.1016/j.pmrj.2013.05.009
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Schneider, M.B., Manikowski, A., Cohen, L. et al. The distinct longitudinal impact of pain catastrophizing on pain interference among youth living with sickle cell disease and chronic pain. J Behav Med 45, 622–631 (2022). https://doi.org/10.1007/s10865-021-00280-4
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DOI: https://doi.org/10.1007/s10865-021-00280-4