Literature DB >> 20308350

Patient-caregiver concordance in symptom assessment and improvement in outcomes for patients undergoing cancer chemotherapy.

Maria J Silveira1, Charles W Given, Barbara Given, Ann Marie Rosland, John D Piette.   

Abstract

OBJECTIVE: To measure the agreement between cancer patients' and family caregivers' perceptions of the patients' symptom severity, and the association between changes in caregiver accuracy and changes in outcomes.
METHODS: Secondary analysis of baseline and 10-week follow-up data from 142 cancer patient/caregiver dyads. Patient/caregiver agreement about symptom burden was measured for the 8 most prevalent symptoms and overall. Bivariate analyses examined the patient and caregiver characteristics associated with caregivers who were overestimators, underestimators or accurate at baseline. We tested the relationship between change in caregiver accuracy and both caregiver behaviour (e.g. use of information, hours spent caregiving) and patient outcomes (e.g. total symptom severity and frequency).
RESULTS: At baseline, caregivers overestimated the severity of 17 out of 18 symptoms; 50% predicted mean symptom severity accurately. Accuracy worsened over time for 51%, stayed the same for 36%, and improved for 13%. While not statistically significant, caregivers whose accuracy improved over time had patients who reported greater declines in: symptom severity, number of symptoms, symptom interference, total symptom frequency and depression. In addition, these caregivers experienced greater reductions in their use of information and hours helping the patient. DISCUSSION: Caregivers typically over-estimate cancer patients' symptom burden and accuracy does not improve over time. Improving caregiver accuracy may boost the positive effects of cognitive behavioural interventions designed to improve cancer patients' quality of life.

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Year:  2010        PMID: 20308350     DOI: 10.1177/1742395309359208

Source DB:  PubMed          Journal:  Chronic Illn        ISSN: 1742-3953


  18 in total

1.  Perceived mental health status of drug users with HIV: concordance between caregivers and care recipient reports and associations with caregiving burden and reciprocity.

Authors:  Mary M Mitchell; Allysha C Robinson; Jennifer L Wolff; Amy R Knowlton
Journal:  AIDS Behav       Date:  2014-06

2.  Symptom burden in palliative care patients: perspectives of patients, their family caregivers, and their attending physicians.

Authors:  Karin Oechsle; Kathrin Goerth; Carsten Bokemeyer; Anja Mehnert
Journal:  Support Care Cancer       Date:  2013-02-21       Impact factor: 3.603

3.  Couples' symptom burden in oncology care: perception of self and the other.

Authors:  Gabriel Lopez; Kathrin Milbury; Minxing Chen; Yisheng Li; Eduardo Bruera; Lorenzo Cohen
Journal:  Support Care Cancer       Date:  2018-06-09       Impact factor: 3.603

4.  A tool to strengthen the older patient-companion partnership in primary care: results from a pilot study.

Authors:  Jennifer L Wolff; Debra L Roter; Jeremy Barron; Cynthia M Boyd; Bruce Leff; Thomas E Finucane; Joseph J Gallo; Peter V Rabins; David L Roth; Laura N Gitlin
Journal:  J Am Geriatr Soc       Date:  2014-01-13       Impact factor: 5.562

5.  Nonspecific Symptoms Lack Diagnostic Accuracy for Infection in Older Patients in the Emergency Department.

Authors:  Jeffrey M Caterino; David M Kline; Robert Leininger; Lauren T Southerland; Christopher R Carpenter; Christopher W Baugh; Daniel J Pallin; Katherine M Hunold; Kurt B Stevenson
Journal:  J Am Geriatr Soc       Date:  2018-11-22       Impact factor: 5.562

6.  Patient-Family Agenda Setting for Primary Care Patients with Cognitive Impairment: the SAME Page Trial.

Authors:  Jennifer L Wolff; Debra L Roter; Cynthia M Boyd; David L Roth; Diane M Echavarria; Jennifer Aufill; Judith B Vick; Laura N Gitlin
Journal:  J Gen Intern Med       Date:  2018-07-18       Impact factor: 5.128

7.  Prognostic Understanding at Diagnosis and Associated Factors in Patients with Advanced Lung Cancer and Their Caregivers.

Authors:  Takashi Sato; Kenzo Soejima; Daisuke Fujisawa; Mari Takeuchi; Daisuke Arai; Ichiro Nakachi; Katsuhiko Naoki; Ichiro Kawada; Hiroyuki Yasuda; Kota Ishioka; Shigenari Nukaga; Keigo Kobayashi; Katsunori Masaki; Takashi Inoue; Kota Hikima; Morio Nakamura; Keiko Ohgino; Yoshitaka Oyamada; Yohei Funatsu; Takeshi Terashima; Naoki Miyao; Koichi Sayama; Fumitake Saito; Fumio Sakamaki; Tomoko Betsuyaku
Journal:  Oncologist       Date:  2018-08-17

8.  Before Hospice: Symptom Burden, Dementia, and Social Participation in the Last Year of Life.

Authors:  Halima Amjad; Scott H Snyder; Jennifer L Wolff; Esther Oh; Quincy M Samus
Journal:  J Palliat Med       Date:  2019-05-06       Impact factor: 2.947

9.  Symptom burden in chronically ill homebound individuals.

Authors:  Ania Wajnberg; Katherine Ornstein; Meng Zhang; Kristofer L Smith; Theresa Soriano
Journal:  J Am Geriatr Soc       Date:  2012-12-03       Impact factor: 5.562

10.  Association Between Symptom Burden and Time to Hospitalization, Nursing Home Placement, and Death Among the Chronically Ill Urban Homebound.

Authors:  Nancy Yang; Katherine A Ornstein; Jennifer M Reckrey
Journal:  J Pain Symptom Manage       Date:  2016-03-24       Impact factor: 3.612

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