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Late Transitions and Bereaved Family Member Perceptions of Quality of End‐of‐Life Care
dc.contributor.authorMakaroun, Lena K.
dc.contributor.authorTeno, Joan M.
dc.contributor.authorFreedman, Vicki A.
dc.contributor.authorKasper, Judith D.
dc.contributor.authorGozalo, Pedro
dc.contributor.authorMor, Vincent
dc.date.accessioned2018-11-20T15:35:20Z
dc.date.available2019-11-01T15:10:33Zen
dc.date.issued2018-09
dc.identifier.citationMakaroun, Lena K.; Teno, Joan M.; Freedman, Vicki A.; Kasper, Judith D.; Gozalo, Pedro; Mor, Vincent (2018). "Late Transitions and Bereaved Family Member Perceptions of Quality of End‐of‐Life Care." Journal of the American Geriatrics Society 66(9): 1730-1736.
dc.identifier.issn0002-8614
dc.identifier.issn1532-5415
dc.identifier.urihttps://hdl.handle.net/2027.42/146458
dc.publisherJohns Hopkins University School of Public Health
dc.publisherWiley Periodicals, Inc.
dc.subject.otherquality of care
dc.subject.otherhealthcare transitions
dc.subject.otherend‐of‐life care
dc.titleLate Transitions and Bereaved Family Member Perceptions of Quality of End‐of‐Life Care
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelGeriatrics
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/146458/1/jgs15455.pdf
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/146458/2/jgs15455_am.pdf
dc.identifier.doi10.1111/jgs.15455
dc.identifier.sourceJournal of the American Geriatrics Society
dc.identifier.citedreferenceQuigley Denise D., Elliott Marc N., Setodji Claude Messan, Hays Ron D. Quantifying magnitude of group‐level differences in patient experiences with health care. Health Serv Res 2018 Feb 12. doi: 10.1111/1475-6773.12828. [Epub ahead of print]
dc.identifier.citedreferenceTeno JM, Clarridge BR, Casey V, et al. Family perspectives on end‐of‐life care at the last place of care. JAMA 2004; 291: 88 – 93.
dc.identifier.citedreferenceWright AA, Keating NL, Ayanian JZ et al. Family perspectives on aggressive cancer care near the end of life. JAMA 2016; 315: 284 – 292.
dc.identifier.citedreferenceWright AA, Keating NL, Balboni TA, Matulonis UA, Block SD, Prigerson HG. Place of death: Correlations with quality of life of patients with cancer and predictors of bereaved caregivers’ mental health. J Clin Oncol 2010; 28: 4457 – 4464.
dc.identifier.citedreferenceKasper JD, Freedman VA. National Health and Aging Trends Study User Guide: Rounds 1, 2, 3, 4 & 5 Final Release. Baltimore: Johns Hopkins University School of Public Health; 2016 [cited 2017 Jun 22]. Available from: www.NHATS.org
dc.identifier.citedreferenceMontaquila J, Freedman VA, Edwards B, Kasper JD. National Health and Aging Trends Study Round 1 Sample Design and Selection. NHATS Technical Paper #1 [Internet] 2012. Available from: www.NHATS.org
dc.identifier.citedreferenceKasper JD, Freedman VA. National Health and Aging Trends Study User Guide: Rounds 1–6 Beta Release. [Internet]. Baltimore: Johns Hopkins University School of Public Health; 2017 July (online). Available from: www.NHATS.org Accessed September 14, 2017.
dc.identifier.citedreferenceHarrison A, Verhoef M. Understanding coordination of care from the consumer’s perspective in a regional health system. Health Serv Res 2002; 37: 1031 – 1054.
dc.identifier.citedreferencevom Eigen KA, Walker JD, Edgman‐Levitan S, Cleary PD, Delbanco TL. Carepartner experiences with hospital care. Med Care 1999; 37: 33 – 38.
dc.identifier.citedreferenceWeaver FM, Perloff L, Waters T. Patients’ and caregivers’ transition from hospital to home: Needs and recommendations. Home Health Care Serv Q 1998; 17: 27 – 48.
dc.identifier.citedreferenceFuji KT, Abbott AA, Norris JF. Exploring care transitions from patient, caregiver, and health‐care provider perspectives. Clin Nurs Res 2013; 22: 258 – 274.
dc.identifier.citedreferenceWasserstein RL, Lazar NA. The ASA’s statement on p‐values: Context, process, and purpose. Am Stat 2016; 70: 129 – 133.
dc.identifier.citedreferenceCumming G. The new statistics: Why and how. Psychol Sci 2014; 25: 7 – 29.
dc.identifier.citedreferenceAnhang Price R, Stucky B, Parast L et al. Development of valid and reliable measures of patient and family experiences of hospice care for public reporting. J Palliat Med 2018 Mar 20. doi: 10.1089/jpm.2017.0594. [Epub ahead of print]
dc.identifier.citedreferenceShield RR, Wetle T, Teno J, Miller SC, Welch LC. Vigilant at the end of life: Family advocacy in the nursing home. J Palliat Med 2010 26;13: 573 – 579.
dc.identifier.citedreferenceWetle T, Shield R, Teno J, Miller SC, Welch L. Family perspectives on end‐of‐life care experiences in nursing homes. Gerontologist 2005; 45: 642 – 650.
dc.identifier.citedreferenceShield RR, Wetle T, Teno J, Miller SC, Welch L. Physicians “missing in action”: Family perspectives on physician and staffing problems in end‐of‐life care in the nursing home. J Am Geriatr Soc 2005; 53: 1651 – 1657.
dc.identifier.citedreferenceColeman EA, Parry C, Chalmers S, Min S. The Care Transitions Intervention: Results of a randomized controlled trial. Arch Intern Med 2006; 166: 1822 – 1828.
dc.identifier.citedreferenceVoss R, Gardner R, Baier R, Butterfield K, Lehrman S, Gravenstein S. The Care Transitions Intervention: Translating from efficacy to effectiveness. Arch Intern Med 2011; 171: 1232 – 1237.
dc.identifier.citedreferenceHirschman KB, Shaid E, McCauley K, Pauly MV, Naylor MD. Continuity of dare: The transitional care model. Online J Issues Nurs 2015; 20: 1.
dc.identifier.citedreferenceTeno JM, Weitzen S, Fennell ML, Mor V. Dying trajectory in the last year of life: Does cancer trajectory fit other diseases? J Palliat Med 2001; 4: 457 – 464.
dc.identifier.citedreferenceLunney JR, Lynn J, Foley DJ, Lipson S, Guralnik JM. Patterns of functional decline at the end of life. JAMA 2003; 289: 2387 – 2392.
dc.identifier.citedreferenceCovinsky KE, Eng C, Lui L‐Y, Sands LP, Yaffe K. The last 2 years of life: Functional trajectories of frail older people. J Am Geriatr Soc 2003; 51: 492 – 498.
dc.identifier.citedreferenceBoockvar K, Fishman E, Kyriacou CK, Monias A, Gavi S, Cortes T. Adverse events due to discontinuations in drug use and dose changes in patients transferred between acute and long‐term care facilities. Arch Intern Med 2004; 164: 545 – 550.
dc.identifier.citedreferenceField TS, Gurwitz JH, Avorn J et al. Risk factors for adverse drug events among nursing home residents. Arch Intern Med 2001; 161: 1629 – 1634.
dc.identifier.citedreferenceColeman EA. Falling through the cracks: Challenges and opportunities for improving transitional care for persons with continuous complex care needs. J Am Geriatr Soc 2003; 51: 549 – 555.
dc.identifier.citedreferenceMoore C, Wisnivesky J, Williams S, McGinn T. Medical errors related to discontinuity of care from an inpatient to an outpatient setting. J Gen Intern Med 2003; 18: 646 – 651.
dc.identifier.citedreferenceGozalo P, Teno JM, Mitchell SL et al. End‐of‐life transitions among nursing home residents with cognitive issues. N Engl J Med 2011 29;365: 1212 – 1221.
dc.identifier.citedreferenceTeno JM, Gozalo PL, Bynum JW et al. Change in end‐of‐life care for Medicare beneficiaries: Site of death, place of care, and health care transitions in 2000, 2005, and 2009. JAMA 2013; 309: 470 – 477.
dc.identifier.citedreferenceWetle T, Teno J, Shield R, Welch L, Miller SC. End of Life in Nursing Homes: Experiences and Policy Recommendations [Internet]. Washington, DC: AARP; 2004 Nov (online). Available at: http://assets.aarp.org/rgcenter/health/2004_14_eol.pdf Accessed September 16, 2016.
dc.identifier.citedreferenceTeno JM, Lima JC, Lyons KD. Cancer patient assessment and reports of excellence: Reliability and validity of advanced cancer patient perceptions of the quality of care. J Clin Oncol 2009; 27: 1621 – 1626.
dc.identifier.citedreferenceSinger PA, Martin DK, Kelner M. Quality end‐of‐life care: patients’ perspectives. JAMA 1999; 281: 163 – 168.
dc.identifier.citedreferenceSteinhauser KE, Clipp EC, McNeilly M, Christakis NA, McIntyre LM, Tulsky JA. In search of a good death: Observations of patients, families, and providers. Ann Intern Med 2000; 132: 825 – 832.
dc.identifier.citedreferenceMcPherson CJ, Addington‐Hall JM. Judging the quality of care at the end of life: Can proxies provide reliable information? Soc Sci Med 2003; 56: 95 – 109.
dc.identifier.citedreferenceTeno JM, Casey VA, Welch LC, Edgman‐Levitan S. Patient‐focused, family‐centered end‐of‐life medical care. J Pain Symptom Manage 2001; 22: 738 – 751.
dc.identifier.citedreferenceTeno JM, Clarridge B, Casey V, Edgman‐Levitan S, Fowler J. Validation of toolkit after‐death bereaved family member interview. J Pain Symptom Manage 2001; 22: 752 – 758.
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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