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Psychological distress and unsatisfied need for psychosocial support in adolescent and young adult cancer patients during the first year following diagnosis
dc.contributor.authorZebrack, Brad J.en_US
dc.contributor.authorCorbett, Virginiaen_US
dc.contributor.authorEmbry, Leanneen_US
dc.contributor.authorAguilar, Christineen_US
dc.contributor.authorMeeske, Kathleen A.en_US
dc.contributor.authorHayes‐lattin, Brandonen_US
dc.contributor.authorBlock, Rebeccaen_US
dc.contributor.authorZeman, David T.en_US
dc.contributor.authorCole, Stevenen_US
dc.date.accessioned2014-11-04T16:35:38Z
dc.date.availableWITHHELD_13_MONTHSen_US
dc.date.available2014-11-04T16:35:38Z
dc.date.issued2014-11en_US
dc.identifier.citationZebrack, Brad J.; Corbett, Virginia; Embry, Leanne; Aguilar, Christine; Meeske, Kathleen A.; Hayes‐lattin, Brandon ; Block, Rebecca; Zeman, David T.; Cole, Steven (2014). "Psychological distress and unsatisfied need for psychosocial support in adolescent and young adult cancer patients during the first year following diagnosis." Psychoâ Oncology 23(11): 1267-1275.en_US
dc.identifier.issn1057-9249en_US
dc.identifier.issn1099-1611en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/109318
dc.description.abstractPurpose Identifying at‐risk adolescent and young adult (AYA) cancer patients and referring them to age‐appropriate psychosocial support services may be instrumental in reducing psychological distress and promoting psychosocial adaptation. The purpose of this study is to identify trajectories of clinically significant levels of distress throughout the first year following diagnosis and to distinguish factors, including supportive care service use, that predict the extent to which AYAs report distress. Methods In this prospective multisite study, 215 AYAs aged 15–39 years were assessed for psychological distress and psychosocial support service use within the first 4 months of diagnosis and again 6 and 12 months later. On the basis of distress scores, respondents were assigned to one of four distress trajectory groups (Resilient, Recovery, Delayed, and Chronic). Multiple logistic regression analyses examined whether demographics, clinical variables, and reports of unsatisfied need for psychosocial support were associated with distress trajectories over 1 year. Results Twelve percent of AYAs reported clinically significant chronic distress throughout the first 12 months following diagnosis. An additional 15% reported delayed distress. Substantial proportions of AYAs reported that needs for information (57%), counseling (41%), and practical support (39%) remained unsatisfied at 12 months following diagnosis. Not getting counseling needs met, particularly with regard to professional mental health services, was observed to be significantly associated with distress over time. Conclusions Substantial proportions of AYAs are not utilizing psychosocial support services. Findings suggest the importance of identifying psychologically distressed AYAs and addressing their needs for mental health counseling throughout a continuum of care. Copyright © 2014 John Wiley & Sons, Ltd.en_US
dc.publisherSpringer‐Verlagen_US
dc.publisherWiley Periodicals, Inc.en_US
dc.subject.otherAdolescenten_US
dc.subject.otherYoung Adulten_US
dc.subject.otherDistressen_US
dc.subject.otherPsychosocialen_US
dc.titlePsychological distress and unsatisfied need for psychosocial support in adolescent and young adult cancer patients during the first year following diagnosisen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelHematology and Oncologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/109318/1/pon3533.pdf
dc.identifier.doi10.1002/pon.3533en_US
dc.identifier.sourcePsycho‐Oncologyen_US
dc.identifier.citedreferenceCostanzo ES, Ryff CD, Singer BH. Psychosocial adjustment among cancer survivors: findings from a national survey of health and well‐being. Health Psychol 2009; 28: 147 – 156.en_US
dc.identifier.citedreferenceZebrack B. Information and service needs for young adult cancer survivors. Support Care Cancer 2009; 17: 349 – 357.en_US
dc.identifier.citedreferenceZebrack BJ. Information and service needs for young adult cancer patients. Support Care Cancer 2008; 16: 1353 – 1360.en_US
dc.identifier.citedreferenceZebrack BJ, Chesler MA. Managed care: the new context for social work in health care – implications for survivors of childhood cancer and their families. Soc Work Health Care 2000; 31 ( 2 ): 89 – 104.en_US
dc.identifier.citedreferenceHowlader N, et al. SEER cancer statistics review, 1975–2008. 2011; (Available from: http://seer.cancer.gov/csr/1975_2008/ ) [March 14, 2014].en_US
dc.identifier.citedreferenceBleyer A. Latest estimates of survival rates of the 24 most common cancers in adolescent and young adult Americans. J Adolescent and Young Adult Oncol 2011; 1 ( 1 ): 37 – 41.en_US
dc.identifier.citedreferenceStava CJ, Lopez A, Vassilopoulou‐Sellin R. Health profiles of younger and older breast cancer survivors. Cancer 2006; 107 ( 8 ): 1752 – 1759.en_US
dc.identifier.citedreferenceMor V, Allen S, Malin M. The psychosocial impact of cancer on older versus younger patients and their families. Cancer 1994; 74: 2118 – 2127.en_US
dc.identifier.citedreferenceGanz PA, et al. The psychosocial impact of cancer on the elderly: a comparison with younger patients. J Am Geriatr Soc 1985; 33: 429 – 435.en_US
dc.identifier.citedreferenceParker PA, et al. Psychosocial and demographic predictors of quality of life in a large sample of cancer patients. Psycho‐Oncology 2003; 12: 183 – 193.en_US
dc.identifier.citedreferenceReeves WC, et al. Mental illness surveillance among adults in the United States, in Morbidity and Mortality Weekly Report, C.f.D.C.a. Prevention, Editor, Centers for Disease Control and Prevention: Atlanta, GA. p. 1‐32, 2011.en_US
dc.identifier.citedreferenceAdolescent and Young Adult Oncology Progress Review Group. Closing the gap: research and care imperatives for adolescents and young adults with cancer, in Report of the Adolescent and Young Adult Oncology Progress Review Group August 2006. (Available from: http://planning.cancer.gov/disease/AYAO_PRG_Report_2006_FINAL.pdf ), US Department of Health and Human Services, National Institutes of Health, National Cancer Institute; and the LiveSTRONG Young Adult Alliance, NIH Publication No. 06‐6067: Bethesda, MD.en_US
dc.identifier.citedreferenceFerrari A, et al. Starting an adolescent and young adult program: some success stories and some obstacles to overcome. J Clin Oncol 2010; 28 ( 32 ): 4850 – 4857.en_US
dc.identifier.citedreferenceBleyer A, Viny A, Barr RD. Cancer Epidemiology in Older Adolescents and Young Adults 15 to 29 Years: SEER Incidence and Survival, 1975‐2000, National Cancer Institute, NIH Pub. No. 06‐5767: Bethesda, MD, 2006.en_US
dc.identifier.citedreferenceBarakat LP, Alderfer MA, Kazak AE. Posttraumatic growth in adolescent survivors of cancer and their mothers and fathers. J Pediatr Psychol 2006; 31 ( 4 ): 413 – 419.en_US
dc.identifier.citedreferenceStanton AL, Bower JE, Low CA. Posttraumatic growth after cancer. In Handbook of Posttraumatic Growth: Research and Practice, Calhoun L, Tedeschi R, (eds.), Lawrence Erlbaum Associates, Inc.: Mahwah. 2006; 138 – 175.en_US
dc.identifier.citedreferenceBonanno GA, Diminich ED. Annual research review: positive adjustment to adversity – trajectories of minimal‐impact resilience and emergent resilience. J Child Psychol Psyc 2013; 54 ( 4 ): 378 – 401.en_US
dc.identifier.citedreferenceHaase JE. The adolescent resilience model as a guide to interventions. J Pediatr Oncol Nurs 2004; 21 ( 5 ): 289 – 299.en_US
dc.identifier.citedreferenceButow PN, et al. Review of adherence‐related issues in adolescents and young adults with cancer. J Clin Oncol 2010; 28 ( 32 ): 4800 – 4809.en_US
dc.identifier.citedreferenceSansom‐Daly U, et al. A systematic review of psychological interventions for adolecents and young adults living with chronic illness. Health Psychol 2011. DOI: 10.1037/a0025977.en_US
dc.identifier.citedreferenceSeitz DC, Besier T, Goldbeck L. Psychosocial interventions for adolescent cancer patients: a systematic review of the literature. Psycho‐Oncology 2009; 18 ( 7 ): 683 – 690.en_US
dc.identifier.citedreferenceInstitute of Medicine. From Cancer Patient to Cancer Survivor: Lost in Transition, Hewitt M, Greenfield S, Stovall E (eds.), National Academies Press: Washington, DC, 2006.en_US
dc.identifier.citedreferenceRecklitis CJ, Rodriguez P. Screening childhood cancer survivors with the brief symptom inventory‐18: classification agreement with the symptom checklist‐90‐revised. Psycho‐Oncology 2007; 16: 429 – 436.en_US
dc.identifier.citedreferenceParry C, Chesler M. Thematic evidence of psychosocial thriving in survivors of childhood cancer. Qual Health Res 2005; 15 ( 8 ): 1055 – 1073.en_US
dc.identifier.citedreferenceWoodgate RL. A review of the literature on resilience in the adolescent with cancer: part II. J Pediatr Oncol Nurs 1997; 16 ( 2 ): 78 – 89.en_US
dc.identifier.citedreferenceZebrack BJ, Chesler MA, Penn A. Psychosocial support. In Cancer in Adolescents and Young Adults, Bleyer WA, Barr RD, (eds.), Springer‐Verlag: Berlin Heidelberg, 2007.en_US
dc.identifier.citedreferenceMorgan S, et al. Sex, drugs, and rock 'n' roll: caring for adolescents and young adults with cancer. J Clin Oncol 2010; 28 ( 32 ): 4825 – 4830.en_US
dc.identifier.citedreferencePalmer S, Thomas D. A practice framework for working with 15‐25 year‐old cancer patients treated within the adult health sector, Melbourne, Australia, onTrac@PeterMac Victorian Adolescent and Young Adult Cancer Service. 2008. (Available from: http://www1.petermac.org/ontrac/pdf/AYA‐Practice‐Framework.pdf ) [March 14, 2014].en_US
dc.identifier.citedreferenceD'Agostino NM, Penney A, Zebrack B. Providing developmentally appropriate psychosocial care to adolescent and young adult cancer survivors. Cancer, 2011; 117 ( 10 Supplement ): 2329 – 2334.en_US
dc.identifier.citedreferenceZebrack B, Isaacson S. Psychosocial care of adolescent and young adult (AYA) cancer patients and survivors. J Clin Oncol 2012; 30 ( 11 ): 1221 – 1226.en_US
dc.identifier.citedreferenceKeegan THM, et al. Unmet adolescent and young adult cancer survivors information and service needs: a population‐based cancer registry study. J Cancer Survivorship: Res Pract 2012; 6: 239 – 250.en_US
dc.identifier.citedreferenceDyson GJ, et al. The relationship between unmet needs and distress amongst young people with cancer. Support Care Cancer 2012; 20: 75 – 85.en_US
dc.identifier.citedreferenceZebrack B, et al. Psychosocial service use and unmet need among recently diagnosed adolescent and young adult cancer patients. Cancer 2013; 119: 201 – 214.en_US
dc.identifier.citedreferenceZabora JR et al. The prevalence of psychological distress by cancer site. Psycho‐Oncology 2001; 10: 19 – 28.en_US
dc.identifier.citedreferenceCarlson LE, et al. High levels of untreated distress and fatigue in cancer patients. Br J Cancer 2004; 90: 2297 – 2304.en_US
dc.identifier.citedreferenceHedstrom M, Ljungman G, von Essen L. Perceptions of distress among adolescents recently diagnosed with cancer. J Pediat Hematol Oncol 2005; 27: 15 – 22.en_US
dc.identifier.citedreferenceKwak M, et al. Trajectories of psychological distress in adolescent and young adult cancer patients: a one‐year longitudinal study. J Clin Oncol 2013; 31 ( 17 ): 2160 – 2166.en_US
dc.identifier.citedreferenceRowland JH. Developmental stage and adaptation: adult model. In Handbook of Psycho‐Oncology, Chapter 3, Holland JC, Rowland JH, (eds.). Oxford University Press: New York, NY, 1990.en_US
dc.identifier.citedreferenceLazarus R, Folkman S. Stress, Appraisal and Coping. Springer: New York, 1984.en_US
dc.identifier.citedreferenceBenjamin HH. From Victim to Victor, Dell: New York, 1989.en_US
dc.identifier.citedreferenceStanton AL, et al. Promoting adjustment after treatment for cancer. Cancer 2005; 104 ( 11 Suppl ): 2608 – 2613.en_US
dc.identifier.citedreferenceMerluzzi TV, et al. Self‐efficacy for coping with cancer: revision of the Cancer Behavior Inventory (Version 2.0). Psycho‐Oncology 2001; 10: 206 – 217.en_US
dc.identifier.citedreferenceAdler NE, Page A. Cancer Care for the Whole Patient: Meeting Psychosocial Health Needs, National Academies Press: Washington, DC, 2008.en_US
dc.identifier.citedreferencePirl WF, Jacobsen PB, DeShields TL. Opportunities for improving psychosocial care for cancer survivors. J Clin Oncol 2013; 31 ( 16 ): 1920 – 1921.en_US
dc.identifier.citedreferenceForsythe LP, et al. Receipt of psychosocial care among cancer survivors in the United States. J Clin Oncol 2013; 31 ( 16 ): 1961 – 1969.en_US
dc.identifier.citedreferenceBonanno GA. Loss, trauma, and human resilience: have we underestimated the human capacity to thrive after extremely aversive events? Am Psychol 2004; 59 ( 1 ): 20 – 28.en_US
dc.identifier.citedreferenceDerogatis L. BSI 18 Brief Symptom Inventory 18, Administration, Scoring, and Procedures Manual. NCS Pearson, Inc.: Minneapolis, MN, 2000en_US
dc.identifier.citedreferenceDerogatis LR. BSI Brief Symptom Inventory: Administration, Scoring, and Procedures Manual, National Computer Systems, Inc.: Minneapolis, MN, 1993.en_US
dc.identifier.citedreferenceCarlson LE, Bultz BD. Cancer distress screening: needs, methods, and models. J Psychosom Res 2003; 55: 403 – 409.en_US
dc.identifier.citedreferenceRohan EA. Removing the stress from selecting instruments: arming social workers to take leadership in routine distress screening implementation. J Psychosoc Oncol 2012; 30 ( 6 ): 667 – 678.en_US
dc.identifier.citedreferenceJacobsen PB, et al. Screening for psychologic distress in ambulatory cancer patients. Cancer 2005; 103: 1494 – 1502.en_US
dc.identifier.citedreferenceRecklitis CJ, et al. Factor structure of the Brief Symptom Inventory–18 in adult survivors of childhood cancer: results from the Childhood Cancer Survivor Study. Psychol Assess 2006; 18 ( 1 ): 22 – 32.en_US
dc.identifier.citedreferenceChesler M, Barbarin O. Childhood Cancer and the Family, Brunner/Mazel: New York, 1987.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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