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Psychosocial service use and unmet need among recently diagnosed adolescent and young adult cancer patients

dc.contributor.authorZebrack, Brad J.en_US
dc.contributor.authorBlock, Rebeccaen_US
dc.contributor.authorHayes‐lattin, Brandonen_US
dc.contributor.authorEmbry, Leanneen_US
dc.contributor.authorAguilar, Christineen_US
dc.contributor.authorMeeske, Kathleen A.en_US
dc.contributor.authorLi, Yunen_US
dc.contributor.authorButler, Melissaen_US
dc.contributor.authorCole, Stevenen_US
dc.date.accessioned2013-01-03T19:38:48Z
dc.date.available2014-03-03T15:09:24Zen_US
dc.date.issued2013-01-01en_US
dc.identifier.citationZebrack, Brad J.; Block, Rebecca; Hayes‐lattin, Brandon ; Embry, Leanne; Aguilar, Christine; Meeske, Kathleen A.; Li, Yun; Butler, Melissa; Cole, Steven (2013). "Psychosocial service use and unmet need among recently diagnosed adolescent and young adult cancer patients." Cancer 119(1): 201-214. <http://hdl.handle.net/2027.42/94884>en_US
dc.identifier.issn0008-543Xen_US
dc.identifier.issn1097-0142en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/94884
dc.description.abstractBACKGROUND: Adolescents and young adults (AYAs) with cancer demonstrate biomedical risks and psychosocial issues distinct from those of children or older adults. In this study, the authors examined and compared the extent to which AYAs treated in pediatric or adult oncology settings reported use of, and unmet need for, psychosocial support services. METHODS: Within 4 months of initial cancer diagnosis, 215 AYAs ages 14 to 39 years (99 from pediatric care settings and 116 from adult care settings; 75% response rate) were assessed for reporting use of information resources, emotional support services, and practical support services. Statistical analyses derived odds ratios and 95% confidence intervals for service use and unmet needs after controlling for race, employment/school status, sex, relationship status, severity of cancer, treatment, and treatment‐related side effects. RESULTS: AYAs ages 20 to 29 years were significantly less likely than teens and older patients ages 30 to 39 years to report using professional mental health services and were significantly more likely to report an unmet need with regard to cancer information, infertility information, and diet/nutrition information. Compared with teens who were treated in pediatric facilities, AYAs who were treated in adult facilities were more likely to report an unmet need for age‐appropriate Internet sites, professional mental health services, camp/retreats programs, transportation assistance, and complementary and alternative health services. CONCLUSIONS: Substantial proportions of AYAs are not getting their psychosocial care needs met. Bolstering psychosocial support staff and patient referral to community‐based social service agencies and reputable Internet resources may enhance care and improve quality of life for AYAs. Cancer 2013. © 2012 American Cancer Society. Adolescents and young adults with cancer demonstrate biomedical risks and psychosocial issues distinct from those of younger children or older adult patients. The current findings suggest that substantial proportions of these patients are not getting their psychosocial care needs met.en_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherYoung Adulten_US
dc.subject.otherPsychosocialen_US
dc.subject.otherSupportive Careen_US
dc.subject.otherAdolescenten_US
dc.titlePsychosocial service use and unmet need among recently diagnosed adolescent and young adult cancer patientsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan School of Social Work, 1080 S. University, Ann Arbor, MI 48109‐1106en_US
dc.contributor.affiliationumUniversity of Michigan School of Social Work, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Biostatistics, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumCancer Surveillance and Outcomes Research Team, University of Michigan Comprehensive Cancer Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Behavioral Science, University of Michigan, Dearborn, Michiganen_US
dc.contributor.affiliationotherOregon Health and Sciences University, Portland, Oregonen_US
dc.contributor.affiliationotherUniversity of Texas Health Science Center, San Antonio, Texasen_US
dc.contributor.affiliationotherUniversity of Southern California Children's Hospital, Los Angeles, Californiaen_US
dc.contributor.affiliationotherHopeLab Foundation, Redwood City, Californiaen_US
dc.identifier.pmid22744865en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/94884/1/27713_ftp.pdf
dc.identifier.doi10.1002/cncr.27713en_US
dc.identifier.sourceCanceren_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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