Literature DB >> 25782082

Patient characteristics associated with the level of patient-reported care coordination among male patients with colorectal cancer in the Veterans Affairs health care system.

George L Jackson1,2, Leah L Zullig1,2, Sean M Phelan3, Dawn Provenzale1,4, Joan M Griffin5, Steven B Clauser6, David A Haggstrom7,8, Rahul M Jindal9, Michelle van Ryn3.   

Abstract

BACKGROUND: The current study was performed to determine whether patient characteristics, including race/ethnicity, were associated with patient-reported care coordination for patients with colorectal cancer (CRC) who were treated in the Veterans Affairs (VA) health care system, with the goal of better understanding potential goals of quality improvement efforts aimed at improving coordination.
METHODS: The nationwide Cancer Care Assessment and Responsive Evaluation Studies survey involved VA patients with CRC who were diagnosed in 2008 (response rate, 67%). The survey included a 4-item scale of patient-reported frequency ("never," "sometimes," "usually," and "always") of care coordination activities (scale score range, 1-4). Among 913 patients with CRC who provided information regarding care coordination, demographics, and symptoms, multivariable logistic regression was used to examine odds of patients reporting optimal care coordination.
RESULTS: VA patients with CRC were found to report high levels of care coordination (mean scale score, 3.50 [standard deviation, 0.61]). Approximately 85% of patients reported a high level of coordination, including the 43% reporting optimal/highest-level coordination. There was no difference observed in the odds of reporting optimal coordination by race/ethnicity. Patients with early-stage disease (odds ratio [OR], 0.60; 95% confidence interval [95% CI], 0.45-0.81), greater pain (OR, 0.97 for a 1-point increase in pain scale; 95% CI, 0.96-0.99), and greater levels of depression (OR, 0.97 for a 1-point increase in depression scale; 95% CI, 0.96-0.99) were less likely to report optimal coordination.
CONCLUSIONS: Patients with CRC in the VA reported high levels of care coordination. Unlike what has been reported in settings outside the VA, there appears to be no racial/ethnic disparity in reported coordination. However, challenges remain in ensuring coordination of care for patients with less advanced disease and a high symptom burden. Cancer 2015;121:2207-2213.
© 2015 American Cancer Society. © 2015 American Cancer Society.

Entities:  

Keywords:  care coordination; colorectal cancer; health disparities; veterans

Mesh:

Year:  2015        PMID: 25782082      PMCID: PMC4573735          DOI: 10.1002/cncr.29341

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  30 in total

1.  The construction and testing of the EORTC colorectal cancer-specific quality of life questionnaire module (QLQ-CR38). European Organization for Research and Treatment of Cancer Study Group on Quality of Life.

Authors:  M A Sprangers; A te Velde; N K Aaronson
Journal:  Eur J Cancer       Date:  1999-02       Impact factor: 9.162

2.  Patients' perceptions of quality of care for colorectal cancer by race, ethnicity, and language.

Authors:  John Z Ayanian; Alan M Zaslavsky; Edward Guadagnoli; Charles S Fuchs; Kathleen J Yost; Cynthia M Creech; Rosemary D Cress; Lilia C O'Connor; Dee W West; William E Wright
Journal:  J Clin Oncol       Date:  2005-08-22       Impact factor: 44.544

Review 3.  Colorectal cancer model of health disparities: understanding mortality differences in minority populations.

Authors:  Blase N Polite; James J Dignam; Olufunmilayo I Olopade
Journal:  J Clin Oncol       Date:  2006-05-10       Impact factor: 44.544

Review 4.  Building a research consortium of large health systems: the Cancer Research Network.

Authors:  Edward H Wagner; Sarah M Greene; Gene Hart; Terry S Field; Suzanne Fletcher; Ann M Geiger; Lisa J Herrinton; Mark C Hornbrook; Christine C Johnson; Judy Mouchawar; Sharon J Rolnick; Victor J Stevens; Stephen H Taplin; Dennis Tolsma; Thomas M Vogt
Journal:  J Natl Cancer Inst Monogr       Date:  2005

5.  Missing clinical information during primary care visits.

Authors:  Peter C Smith; Rodrigo Araya-Guerra; Caroline Bublitz; Bennett Parnes; L Miriam Dickinson; Rebecca Van Vorst; John M Westfall; Wilson D Pace
Journal:  JAMA       Date:  2005-02-02       Impact factor: 56.272

6.  Health-related quality of life and patient reports about care outcomes in a multidisciplinary hospital intervention.

Authors:  Ron D Hays; Jo-Ann Eastwood; Jenny Kotlerman; Karen L Spritzer; Susan L Ettner; Marie Cowan
Journal:  Ann Behav Med       Date:  2006-04

Review 7.  A framework for improving the quality of cancer care: the case of breast and cervical cancer screening.

Authors:  Jane G Zapka; Stephen H Taplin; Leif I Solberg; M Michele Manos
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2003-01       Impact factor: 4.254

8.  Patient-reported quality of supportive care among patients with colorectal cancer in the Veterans Affairs Health Care System.

Authors:  Michelle van Ryn; Sean M Phelan; Neeraj K Arora; David A Haggstrom; George L Jackson; S Yousuf Zafar; Joan M Griffin; Leah L Zullig; Dawn Provenzale; Mark W Yeazel; Rahul M Jindal; Steven B Clauser
Journal:  J Clin Oncol       Date:  2014-02-03       Impact factor: 44.544

9.  An examination of racial differences in process and outcome of colorectal cancer care quality among users of the veterans affairs health care system.

Authors:  Leah L Zullig; George L Jackson; Morris Weinberger; Dawn Provenzale; Bryce B Reeve; William R Carpenter
Journal:  Clin Colorectal Cancer       Date:  2013-08-27       Impact factor: 4.481

10.  Race, treatment, and survival among colorectal carcinoma patients in an equal-access medical system.

Authors:  J A Dominitz; G P Samsa; P Landsman; D Provenzale
Journal:  Cancer       Date:  1998-06-15       Impact factor: 6.860

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  8 in total

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2.  Perceptions of care and patient-reported outcomes in people living with neuroendocrine tumours.

Authors:  Vanessa L Beesley; Matthew Burge; Monica Dumbrava; Jack Callum; Rachel E Neale; David K Wyld
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3.  Concordance of Patient and Caregiver Reports on the Quality of Colorectal Cancer Care.

Authors:  Rachel D Havyer; Michelle van Ryn; Patrick M Wilson; Lauren R Bangerter; Joan M Griffin
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Review 4.  Utility of the Patient-Reported Outcomes Measurement Information System (PROMIS) to measure primary health outcomes in cancer patients: a systematic review.

Authors:  Thi Xuan Mai Tran; Jungeun Park; Joonki Lee; Yuh-Seog Jung; Yoonjung Chang; Hyunsoon Cho
Journal:  Support Care Cancer       Date:  2020-10-15       Impact factor: 3.603

5.  Assessing Patients' Perceptions of Cancer Care Coordination in a Community-Based Setting.

Authors:  Izumi Okado; Kevin Cassel; Ian Pagano; Randall F Holcombe
Journal:  JCO Oncol Pract       Date:  2020-03-27

6.  Differences in patient perceptions of integrated care among black, hispanic, and white Medicare beneficiaries.

Authors:  Emilia J Ling; Molly Frean; Jody So; Maike Tietschert; Nancy Song; Christian Covington; Hassina Bahadurazada; Sonia Khurana; Luis Garcia; Sara J Singer
Journal:  Health Serv Res       Date:  2021-02-11       Impact factor: 3.734

7.  Racial and Ethnic Differences in Satisfaction with Care Coordination Among VA and non-VA Medicare Beneficiaries.

Authors:  Sai K Loganathan; Jennifer C Hasche; Kevin T Koenig; Samuel C Haffer; Uchenna S Uchendu
Journal:  Health Equity       Date:  2017-04-01

8.  Development and psychometric evaluation of a questionnaire to measure cancer patients' perception of care coordination.

Authors:  Izumi Okado; Kevin Cassel; Ian Pagano; Randall F Holcombe
Journal:  BMC Health Serv Res       Date:  2020-01-21       Impact factor: 2.655

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