Literature DB >> 27992271

Family Perspectives on Hospice Care Experiences of Patients with Cancer.

Pallavi Kumar1, Alexi A Wright1, Laura A Hatfield1, Jennifer S Temel1, Nancy L Keating1.   

Abstract

Purpose To determine whether hospice use by patients with cancer is associated with their families' perceptions of patients' symptoms, goal attainment, and quality of end-of-life (EOL) care. Methods We interviewed 2,307 families of deceased patients with advanced lung or colorectal cancer who were enrolled in the Cancer Care Outcomes Research and Surveillance study (a multiregional, prospective, observational study) and died by 2011. We used propensity-score matching to compare family-reported outcomes for patients who did and did not receive hospice care, including the presence and relief of common symptoms (ie, pain, dyspnea), concordance with patients' wishes for EOL care and place of death, and quality of EOL care. We also examined associations between hospice length of stay and these outcomes among hospice enrollees. Results In a propensity-score-matched sample of 1,970 individuals, families of patients enrolled in hospice reported more pain in their patient compared with those not enrolled in hospice. However, families of patients enrolled in hospice more often reported that patients received "just the right amount" of pain medicine (80% v 73%; adjusted difference, 7 percentage points; 95% confidence interval [CI], 1 to 12 percentage points) and help with dyspnea (78% v 70%; adjusted difference, 8 percentage points; 95% CI, 2 to 13 percentage points). Families of patients enrolled in hospice also more often reported that patients' EOL wishes were followed (80% v 74%; adjusted difference, 6 percentage points; 95% CI, 2 to 11 percentage points) and "excellent" quality EOL care (57% v 42%; adjusted difference, 15 percentage points; 95% CI, 11 to 20). Families of patients who received > 30 days of hospice care reported the highest quality EOL outcomes. Conclusion Hospice care is associated with better symptom relief, patient-goal attainment, and quality of EOL care. Encouraging earlier and increased hospice enrollment may improve EOL experiences for patients with cancer and their families.

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Year:  2016        PMID: 27992271      PMCID: PMC5455697          DOI: 10.1200/JCO.2016.68.9257

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  28 in total

1.  Letting go of the rope--aggressive treatment, hospice care, and open access.

Authors:  Alexi A Wright; Ingrid T Katz
Journal:  N Engl J Med       Date:  2007-07-26       Impact factor: 91.245

2.  Length of home hospice care, family-perceived timing of referrals, perceived quality of care, and quality of death and dying in terminally ill cancer patients who died at home.

Authors:  Akemi Yamagishi; Tatsuya Morita; Shohei Kawagoe; Megumi Shimizu; Taketoshi Ozawa; Emi An; Makoto Kobayakawa; Satoru Tsuneto; Yasuo Shima; Mitsunori Miyashita
Journal:  Support Care Cancer       Date:  2014-08-21       Impact factor: 3.603

3.  Family Perspectives on Aggressive Cancer Care Near the End of Life.

Authors:  Alexi A Wright; Nancy L Keating; John Z Ayanian; Elizabeth A Chrischilles; Katherine L Kahn; Christine S Ritchie; Jane C Weeks; Craig C Earle; Mary B Landrum
Journal:  JAMA       Date:  2016-01-19       Impact factor: 56.272

4.  Association between the Medicare hospice benefit and health care utilization and costs for patients with poor-prognosis cancer.

Authors:  Ziad Obermeyer; Maggie Makar; Samer Abujaber; Francesca Dominici; Susan Block; David M Cutler
Journal:  JAMA       Date:  2014-11-12       Impact factor: 56.272

5.  Late referral to hospice and bereaved family member perception of quality of end-of-life care.

Authors:  Erica R Schockett; Joan M Teno; Susan C Miller; Brad Stuart
Journal:  J Pain Symptom Manage       Date:  2005-11       Impact factor: 3.612

6.  Change in end-of-life care for Medicare beneficiaries: site of death, place of care, and health care transitions in 2000, 2005, and 2009.

Authors:  Joan M Teno; Pedro L Gozalo; Julie P W Bynum; Natalie E Leland; Susan C Miller; Nancy E Morden; Thomas Scupp; David C Goodman; Vincent Mor
Journal:  JAMA       Date:  2013-02-06       Impact factor: 56.272

7.  How does the timing of hospice referral influence hospice care in the last days of life?

Authors:  Susan C Miller; Barry Kinzbrunner; Peggy Pettit; J Richard Williams
Journal:  J Am Geriatr Soc       Date:  2003-06       Impact factor: 5.562

8.  Family perspectives on end-of-life care at the last place of care.

Authors:  Joan M Teno; Brian R Clarridge; Virginia Casey; Lisa C Welch; Terrie Wetle; Renee Shield; Vincent Mor
Journal:  JAMA       Date:  2004-01-07       Impact factor: 56.272

9.  The terrible choice: re-evaluating hospice eligibility criteria for cancer.

Authors:  David J Casarett; Jessica M Fishman; Hien L Lu; Peter J O'Dwyer; Frances K Barg; Mary D Naylor; David A Asch
Journal:  J Clin Oncol       Date:  2008-12-29       Impact factor: 44.544

10.  End-of-life care for older patients with ovarian cancer is intensive despite high rates of hospice use.

Authors:  Alexi A Wright; Laura A Hatfield; Craig C Earle; Nancy L Keating
Journal:  J Clin Oncol       Date:  2014-10-06       Impact factor: 44.544

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  19 in total

1.  The Affordable Care Act and End-of-Life Care for Patients With Cancer.

Authors:  Ravi B Parikh; Alexi A Wright
Journal:  Cancer J       Date:  2017 May/Jun       Impact factor: 3.360

2.  The HOPE Pilot Study: Harnessing Patient-Reported Outcomes and Biometric Data to Enhance Cancer Care.

Authors:  Alexi A Wright; Nikita Raman; Patrick Staples; Stephanie Schonholz; Angel Cronin; Kenzie Carlson; Nancy L Keating; Jukka-Pekka Onnela
Journal:  JCO Clin Cancer Inform       Date:  2018-12

3.  Factors Contributing To Geographic Variation In End-Of-Life Expenditures For Cancer Patients.

Authors:  Nancy L Keating; Haiden A Huskamp; Elena Kouri; Deborah Schrag; Mark C Hornbrook; David A Haggstrom; Mary Beth Landrum
Journal:  Health Aff (Millwood)       Date:  2018-07       Impact factor: 6.301

Review 4.  Achieving Goal-Concordant Care: A Conceptual Model and Approach to Measuring Serious Illness Communication and Its Impact.

Authors:  Justin J Sanders; J Randall Curtis; James A Tulsky
Journal:  J Palliat Med       Date:  2017-11-01       Impact factor: 2.947

Review 5.  Easing the Journey-an Updated Review of Palliative Care for the Patient with High-Grade Glioma.

Authors:  Rita C Crooms; Margaret O Johnson; Heather Leeper; Ambereen Mehta; Michelle McWhirter; Akanksha Sharma
Journal:  Curr Oncol Rep       Date:  2022-02-22       Impact factor: 5.075

6.  Comprehensive and Equitable Care for Vulnerable Veterans With Integrated Palliative, Psychology, and Oncology Care.

Authors:  Joanna L Martin; Desiree R Azizoddin; Lauren Z Rynar; Jane Weber; Tyra Oliver; Christine B Weldon; Joshua M Hauser
Journal:  Fed Pract       Date:  2021-08

7.  Associations Between Hospice Care and Scary Family Caregiver Experiences.

Authors:  Elizabeth A Luth; Paul K Maciejewski; Veerawat Phongtankuel; Jiehui Xu; Holly G Prigerson
Journal:  J Pain Symptom Manage       Date:  2020-10-07       Impact factor: 3.612

8.  Hospice Care Experiences Among Cancer Patients and Their Caregivers.

Authors:  Layla Parast; Anagha A Tolpadi; Joan M Teno; Marc N Elliott; Rebecca Anhang Price
Journal:  J Gen Intern Med       Date:  2021-01-19       Impact factor: 5.128

9.  Association Between Delivery System Structure and Intensity of End-of-Life Cancer Care.

Authors:  Lindsey A Herrel; Ziwei Zhu; Jennifer J Griggs; Deborah R Kaye; James M Dupree; Chandy S Ellimoottil; David C Miller
Journal:  JCO Oncol Pract       Date:  2020-02-18

10.  Preoperative Frailty Status and Intensity of End-of-Life Care Among Older Adults After Emergency Surgery.

Authors:  Claire Sokas; Katherine C Lee; Daniel Sturgeon; Jocelyn Streid; Stuart R Lipsitz; Joel S Weissman; Dae H Kim; Zara Cooper
Journal:  J Pain Symptom Manage       Date:  2020-11-16       Impact factor: 5.576

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