Late Transitions and Bereaved Family Member Perceptions of Quality of End‐of‐Life Care
dc.contributor.author | Makaroun, Lena K. | |
dc.contributor.author | Teno, Joan M. | |
dc.contributor.author | Freedman, Vicki A. | |
dc.contributor.author | Kasper, Judith D. | |
dc.contributor.author | Gozalo, Pedro | |
dc.contributor.author | Mor, Vincent | |
dc.date.accessioned | 2018-11-20T15:35:20Z | |
dc.date.available | 2019-11-01T15:10:33Z | en |
dc.date.issued | 2018-09 | |
dc.identifier.citation | Makaroun, 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.issn | 0002-8614 | |
dc.identifier.issn | 1532-5415 | |
dc.identifier.uri | https://hdl.handle.net/2027.42/146458 | |
dc.publisher | Johns Hopkins University School of Public Health | |
dc.publisher | Wiley Periodicals, Inc. | |
dc.subject.other | quality of care | |
dc.subject.other | healthcare transitions | |
dc.subject.other | end‐of‐life care | |
dc.title | Late Transitions and Bereaved Family Member Perceptions of Quality of End‐of‐Life Care | |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | |
dc.subject.hlbsecondlevel | Geriatrics | |
dc.subject.hlbtoplevel | Health Sciences | |
dc.description.peerreviewed | Peer Reviewed | |
dc.description.bitstreamurl | https://deepblue.lib.umich.edu/bitstream/2027.42/146458/1/jgs15455.pdf | |
dc.description.bitstreamurl | https://deepblue.lib.umich.edu/bitstream/2027.42/146458/2/jgs15455_am.pdf | |
dc.identifier.doi | 10.1111/jgs.15455 | |
dc.identifier.source | Journal of the American Geriatrics Society | |
dc.identifier.citedreference | Quigley 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.citedreference | Teno 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.citedreference | Wright 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.citedreference | Wright 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.citedreference | Kasper 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.citedreference | Montaquila 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.citedreference | Kasper 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.citedreference | Harrison 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.citedreference | vom Eigen KA, Walker JD, Edgman‐Levitan S, Cleary PD, Delbanco TL. Carepartner experiences with hospital care. Med Care 1999; 37: 33 – 38. | |
dc.identifier.citedreference | Weaver 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.citedreference | Fuji 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.citedreference | Wasserstein RL, Lazar NA. The ASA’s statement on p‐values: Context, process, and purpose. Am Stat 2016; 70: 129 – 133. | |
dc.identifier.citedreference | Cumming G. The new statistics: Why and how. Psychol Sci 2014; 25: 7 – 29. | |
dc.identifier.citedreference | Anhang 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.citedreference | Shield 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.citedreference | Wetle 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.citedreference | Shield 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.citedreference | Coleman 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.citedreference | Voss 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.citedreference | Hirschman 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.citedreference | Teno 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.citedreference | Lunney 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.citedreference | Covinsky 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.citedreference | Boockvar 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.citedreference | Field 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.citedreference | Coleman 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.citedreference | Moore 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.citedreference | Gozalo 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.citedreference | Teno 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.citedreference | Wetle 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.citedreference | Teno 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.citedreference | Singer PA, Martin DK, Kelner M. Quality end‐of‐life care: patients’ perspectives. JAMA 1999; 281: 163 – 168. | |
dc.identifier.citedreference | Steinhauser 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.citedreference | McPherson 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.citedreference | Teno 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.citedreference | Teno 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.owningcollname | Interdisciplinary and Peer-Reviewed |
Files in this item
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.