Show simple item record

Cancer and Breakthrough Pain's Impact on a Diverse Population

dc.contributor.authorMontague, Lauraen_US
dc.contributor.authorGreen, Carmen R.en_US
dc.date.accessioned2010-06-01T19:47:29Z
dc.date.available2010-06-01T19:47:29Z
dc.date.issued2009-04en_US
dc.identifier.citationMontague, Laura; Green, Carmen R. (2009). "Cancer and Breakthrough Pain's Impact on a Diverse Population." Pain Medicine 10(3): 549-561. <http://hdl.handle.net/2027.42/72924>en_US
dc.identifier.issn1526-2375en_US
dc.identifier.issn1526-4637en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/72924
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=19254338&dopt=citationen_US
dc.description.abstractBackground.  Although breakthrough pain (BTP; pain flares interrupting well-controlled baseline pain) is common among patients with cancer, its prevalence, characteristics, and impact on health-related quality of life (HRQOL) are poorly understood in ethnic minorities. Methods.  This comparative study examines ethnic and gender differences in BTP characteristics and impact on HRQOL. Patients with stage III or IV cancer of the breast, prostate, colorectal, or lung, or stage II–IV multiple myeloma with BTP completed surveys (upon initial assessment, 3 months, and 6 months) assessing consistent pain, BTP, depressed affect, active coping ability, and HRQOL. Results.  Respondents (N = 96) were 75% white, 66% female with a mean age of 56 ± 10 years. All subjects experienced significant psychological distress, but there were no racial differences in depression prevalence. Minorities reported significantly greater severity for consistent pain at its worst ( P  = 0.009), least ( P  ≤ 0.001), on average ( P  = 0.004), and upon initial assessment ( P  = 0.04) as well as greater severity for BTP at its worst ( P  = 0.03), least ( P  = 0.02), and at initial assessment ( P  = 0.008). Although minorities reported more flare types (3.0 vs 1.8, P  = 0.001), there were no significant ethnic differences in the duration, quality, or location of pain flares. Minorities consistently reported poorer outcomes on each HRQOL subscale (physical, role, emotional, cognitive, and social functioning) measured, although not statistically significant, as well as poorer QOL symptom control ( P  = 0.08) including lower dyspnea control ( P  = 0.002). Conclusions.  Overall, minorities experienced greater consistent and breakthrough pain as well as poorer HRQOL. These data suggest further health care disparities in the cancer and pain experience for minorities.en_US
dc.format.extent234433 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Incen_US
dc.rights© 2009 American Academy of Pain Medicineen_US
dc.subject.otherBreakthrough Painen_US
dc.subject.otherCancer Painen_US
dc.subject.otherGenderen_US
dc.subject.otherHealth Care and Health Policyen_US
dc.subject.otherPhysician Variabilityen_US
dc.subject.otherPain Managementen_US
dc.subject.otherRacial and Ethnic Disparitiesen_US
dc.titleCancer and Breakthrough Pain's Impact on a Diverse Populationen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMedicine (General)en_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Health Management and Policy, School of Public Health, University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationother* Department of Anesthesiology, School of Medicine; anden_US
dc.identifier.pmid19254338en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/72924/1/j.1526-4637.2009.00564.x.pdf
dc.identifier.doi10.1111/j.1526-4637.2009.00564.xen_US
dc.identifier.sourcePain Medicineen_US
dc.identifier.citedreferencePortenoy RK, Thaler HT, Kornblith AB, et al. Symptom prevalence, characteristics and distress in a cancer population. Qual Life Res 1994; 3 ( 3 ): 183 – 9.en_US
dc.identifier.citedreferencePortenoy RK, Lesage P. Management of cancer pain. Lancet 1999; 353: 1695 – 700.en_US
dc.identifier.citedreferencePortenoy RK, Hagen NA. Breakthrough pain: Definition, prevalence and characteristics. Pain 1990; 41: 273 – 81.en_US
dc.identifier.citedreferenceBruera E, MacMillan K, Hanson J, MacDonald RN. The Edmonton staging system for cancer pain: Preliminary report. Pain 1989; 37 ( 2 ): 203 – 9.en_US
dc.identifier.citedreferenceBruera E, Fainsinger R, MacEachern T, Hanson J. The use of methylphenidate in patients with incident cancer pain receiving regular opiates. A preliminary report. Pain 1992; 50 ( 1 ): 75 – 7.en_US
dc.identifier.citedreferenceBanning A, Sjogren P, Henriksen H. Treatment outcome in a multidisciplinary cancer pain clinic. Pain 1991; 47 ( 2 ): 129 – 34; discussion 7–8.en_US
dc.identifier.citedreferenceZeppetella G, O'Doherty CA, Collins S. Prevalence and characteristics of breakthrough pain in cancer patients admitted to a hospice. J Pain Symptom Manage 2000; 20 ( 2 ): 87 – 92.en_US
dc.identifier.citedreferencePortenoy RK, Payne D, Jacobsen P. Breakthrough pain: Characteristics and impact in patients with cancer pain. Pain 1999; 81: 129 – 34.en_US
dc.identifier.citedreferencePatt RB, Ellison NM. Breakthrough pain in cancer patients: Characteristics, prevalence, and treatment. Oncology (Huntingt) 1998; 12: 1035 – 46; discussion 49–52.en_US
dc.identifier.citedreferenceCleeland CS, Gonin R, Baez L, Loehrer P, Pandya KJ. Pain and treatment of pain in minority patients with cancer. The Eastern cooperative oncology group minority outpatient pain study. Ann Intern Med 1997; 127: 813 – 6.en_US
dc.identifier.citedreferenceAnderson KO, Richman SP, Hurley J, et al. Cancer pain management among underserved minority outpatients: Perceived needs and barriers to optimal control. Cancer 2002; 94: 2295 – 304.en_US
dc.identifier.citedreferenceDapueto JJ, Servente L, Francolino C, Hahn EA. Determinants of quality of life in patients with cancer. Cancer 2005; 103: 1072 – 81.en_US
dc.identifier.citedreferenceSmedley BD, Stith AY, Nelson AR, eds. Unequal Treatment: Confronting Racial and Ethnic Disparities in Healthcare. Washington, DC: The National Academies Press; 2002.en_US
dc.identifier.citedreferenceHaynes MA, Smedley B, eds. The Unequal Burden of Cancer: An Assessment of NIH Research and Programs for Ethnic Minorities and the Medically Underserved. Washington, DC: National Academy Press; 1999.en_US
dc.identifier.citedreferencePlatz EA, Rimm EB, Willett WC, Kantoff PW, Giovannucci E. Racial variation in prostate cancer incidence and in hormonal system markers among male health professionals. J Natl Cancer Inst 2000; 92: 2009 – 17.en_US
dc.identifier.citedreferenceAgho AO, Lewis MA. Correlates of actual and perceived knowledge of prostate cancer among African Americans. Cancer Nurs 2001; 24: 165 – 71.en_US
dc.identifier.citedreferenceRoetzheim RG, Pal N, Gonzalez EC, et al. Effects of health insurance and race on colorectal cancer treatments and outcomes. Am J Public Health 2000; 90: 1746 – 54.en_US
dc.identifier.citedreferenceCooley ME, Jennings-Dozier K. Lung cancer in African Americans. A call for action. Cancer Pract 1998; 6: 99 – 106.en_US
dc.identifier.citedreferenceNewman LA, Griffith KA, Jatoi I, et al. Meta-analysis of survival in African American and white American patients with breast cancer: Ethnicity compared with socioeconomic status. J Clin Oncol 2006; 24: 1342 – 9.en_US
dc.identifier.citedreferenceGreen CR, Anderson KO, Baker TA, et al. The unequal burden of pain: Confronting racial and ethnic disparities in pain. Pain Med 2003; 4: 277 – 94.en_US
dc.identifier.citedreferenceBonham VL. Race, ethnicity, and pain treatment: Striving to understand the causes and solutions to the disparities in pain treatment. J Law Med Ethics 2001; 29: 52 – 68.en_US
dc.identifier.citedreferenceMcCracken LM, Matthews AK, Tang TS, Cuba SL. A comparison of blacks and whites seeking treatment for chronic pain. Clin J Pain 2001; 17: 249 – 55.en_US
dc.identifier.citedreferenceGreen CR, Baker TA, Sato Y, Washington TL, Smith EM. Race and chronic pain: A comparative study of young black and white Americans presenting for management. J Pain 2003; 4 ( 4 ): 176 – 83.en_US
dc.identifier.citedreferenceGreen CR, Baker TA, Smith EM, Sato Y. The effect of race in older adults presenting for chronic pain management: A comparative study of African and Caucasian Americans. J Pain 2003; 4 ( 2 ): 82 – 90.en_US
dc.identifier.citedreferenceBaker TA, Green CR. Intrarace differences among black and white Americans presenting for chronic pain management: The influence of age, physical health, and psychosocial factors. Pain Med 2005; 6 ( 1 ): 28 – 38.en_US
dc.identifier.citedreferenceNdao-Brumblay SK, Green CR. Racial differences in the physical and psychosocial health among black and white women with chronic pain. J Natl Med Assoc 2005; 97 ( 10 ): 1369 – 77.en_US
dc.identifier.citedreferenceBernabei R, Gambassi G, Lapane K, et al. Management of pain in elderly patients with cancer. SAGE study group. Systematic assessment of geriatric drug use via epidemiology. JAMA 1998; 279 ( 23 ): 1877 – 82.en_US
dc.identifier.citedreferenceGreen CR, Ndao-Brumblay SK, West B, Washington T. Differences in prescription opioid analgesic availability: Comparing minority and white pharmacies across Michigan. J Pain 2005; 6 ( 10 ): 689 – 99.en_US
dc.identifier.citedreferenceBingefors K, Isacson D. Epidemiology, co-morbidity, and impact on health-related quality of life of self-reported headache and musculoskeletal pain–A gender perspective. Eur J Pain 2004; 8 ( 5 ): 435 – 50.en_US
dc.identifier.citedreferenceMiaskowski C. Gender differences in pain, fatigue, and depression in patients with cancer. J Natl Cancer Inst Monogr 2004; 32: 139 – 43.en_US
dc.identifier.citedreferenceMcDowell I, Newell C. Measuring Health: A Guide to Rating Scales and Questionnaires, 2nd edition. New York: Oxford University Press; 1996.en_US
dc.identifier.citedreferenceSchroevers MJ, Sanderman R, van Sonderen E, Ranchor AV. The evaluation of the Center for Epidemiologic Studies depression (CES-D) scale: Depressed and positive affect in cancer patients and healthy reference subjects. Qual Life Res 2000; 9 ( 9 ): 1015 – 29.en_US
dc.identifier.citedreferenceRadloff LS. The CES-D scale: A self-report depression scale for research in the general population. Appl Psychol Meas 1977; 1 ( 3 ): 385 – 401.en_US
dc.identifier.citedreferenceJames SA, Hartnett SA, Kalsbeek WD. John Henryism and blood pressure differences among black men. J Behav Med 1983; 6 ( 3 ): 259 – 78.en_US
dc.identifier.citedreferenceGunnarsdottir S, Donovan HS, Serlin RC, Voge C, Ward S. Patient-related barriers to pain management: The Barriers Questionnaire II (BQ-II). Pain 2002; 99 ( 3 ): 385 – 96.en_US
dc.identifier.citedreferenceAaronson NK, Ahmedzai S, Bergman B, et al. The European Organization for Research and Treatment of Cancer QLQ-C30: A quality-of-life instrument for use in international clinical trials in oncology. J Natl Cancer Inst 1993; 85 ( 5 ): 365 – 76.en_US
dc.identifier.citedreferenceGreen CR, Wheeler JC, LaPorte F, Marchant B, Guerrero E. How well is chronic pain managed? Who does it well? Pain Med 2002; 3 ( 1 ): 56 – 65.en_US
dc.identifier.citedreferenceGreen CR, Wheeler JR. Physician variability in the management of acute postoperative and cancer pain: A quantitative analysis of the Michigan experience. Pain Med 2003; 4 ( 1 ): 8 – 20.en_US
dc.identifier.citedreferenceGreen CR, Wheeler JR, LaPorte F. Clinical decision making in pain management: Contributions of physician and patient characteristics to variations in practice. J Pain 2003; 4 ( 22 ): 29 – 39.en_US
dc.identifier.citedreferenceGreen CR, Wheeler J, Marchant B, LaPorte F, Guerrero E. Analysis of the physician variable in pain management. Pain Med 2001; 2 ( 4 ): 317 – 27.en_US
dc.identifier.citedreferenceLeResche L. Gender considerations in the epidemiology of chronic pain. In: Crombie IK, Croft PR, Linton SJ, LeResche L, VonKorff M, eds. Epidemiology of Pain. Seattle, WA: IASP Press; 1999: 43 – 51.en_US
dc.identifier.citedreferenceGreen CR, Baker TA, Ndao-Brumblay SK. Patient attitudes regarding healthcare utilization and referral: A descriptive comparison in African- and Caucasian Americans with chronic pain. J Natl Med Assoc 2004; 96 ( 1 ): 31 – 42.en_US
dc.identifier.citedreferenceFuentes M, Hart-Johnson T, Green CR. The association among neighborhood socioeconmic status, race and chronic pain in black and white older adults. J Natl Med Assoc 2007; 99 ( 10 ): 1160 – 9.en_US
dc.identifier.citedreferenceMeghani SH, Keane A. Preference for analgesic treatment for cancer pain among African Americans. J Pain Symptom Manage 2007; 34 ( 2 ): 136 – 47.en_US
dc.identifier.citedreferenceCote P, Baldwin ML, Johnson WG. Early patterns of care for occupational back pain. Spine 2005; 30 ( 5 ): 581 – 7.en_US
dc.identifier.citedreferenceStinshoff VJ, Lang EV, Berbaum KS, et al. Effect of sex and gender on drug-seeking behavior during invasive medical procedures. Acad Radiol 2004; 11 ( 4 ): 390 – 7.en_US
dc.identifier.citedreferenceWilliams RE, Black CL, Kim HY, et al. Determinants of healthcare-seeking behaviour among subjects with irritable bowel syndrome. Aliment Pharmacol Ther 2006; 23 ( 11 ): 1667 – 75.en_US
dc.identifier.citedreferenceSmith BH, Elliott AM, Chambers WA, et al. The impact of chronic pain in the community. Fam Pract 2001; 18 ( 3 ): 292 – 9.en_US
dc.identifier.citedreferenceIbrahim SA, Burant CJ, Siminoff LA, Stoller EP, Kwoh CK. Self-assessed global quality of life: A comparison between African-American and white older patients with arthritis. J Clin Epidemiol 2002; 55 ( 5 ): 512 – 7.en_US
dc.identifier.citedreferenceDeshields TL, Tait RC, Gfeller JD, Chibnall JT. Relationship between social desirability and self-report in chronic pain patients. Clin J Pain 1995; 11 ( 3 ): 189 – 93.en_US
dc.identifier.citedreferenceBekelman DB, Dy SM, Becker DM, et al. Spiritual well-being and depression in patients with heart failure. J Gen Intern Med 2007; 22 ( 4 ): 470 – 7.en_US
dc.identifier.citedreferenceBlock SD. Psychological issues in end-of-life care. J Palliat Med 2006; 9 ( 3 ): 751 – 72.en_US
dc.identifier.citedreferenceReich M, Lesur A, Perdrizet-Chevallier C. Depression, quality of life and breast cancer: A review of the literature. Breast Cancer Res Treat 2007; 110 ( 1 ): 9 – 17.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.