Literature DB >> 27603147

Patterns and predictors of colorectal cancer care coordination: A population-based survey of Australian patients.

Ivana Durcinoska1,2, Jane M Young1,2,3, Michael J Solomon2,3.   

Abstract

BACKGROUND: Improving care coordination is a key priority for health services. The aims of this study were to identify patient- and health service-related predictors of poorly coordinated care and to explore patient preferences to assist care coordination.
METHODS: Patients with incident colorectal cancer, identified from a state-wide cancer registry, completed a self-report questionnaire 6 to 8 months after their diagnosis. Care coordination was assessed with the Cancer Care Coordination Questionnaire for Patients. Multiple linear regression models were used to predict factors associated with a poor experience with cancer care coordination.
RESULTS: Among 560 patients (56% response rate), care coordination experiences were normally distributed (mean score, 76.1; standard deviation, 10.9). Patients who had 3 or more comorbid conditions (β, -4.56; standard error [SE], 1.46; P = .006), little or no understanding of the health system (β, -4.34; SE, 0.94; P < .001), and no regular general practitioner (GP; β, -4.09; SE, 2.07; P = .049) experienced poorer care coordination. At the health service level, patients who did not receive a written pretreatment plan (β, -4.15; SE, 0.95; P < .001) or did not see a cancer care coordinator (β, -3.29; SE, 1.03; P = .001) had lower scores. The most preferred resources included information packs (92%), written care plans (88%), and improved access to their own personal medical records (electronic, 86; paper, 84%), with most patients preferring a shared GP and surgeon care model.
CONCLUSIONS: There was wide variation in experiences across the state. The factors associated with lower scores provide a focus for targeted strategies for improving patients' experience with colorectal cancer care coordination. Cancer 2017;123:319-326.
© 2016 American Cancer Society. © 2016 American Cancer Society.

Entities:  

Keywords:  care coordination; colorectal cancer; health services; patient navigation; patient preference; patient-centered care; patient-reported outcome

Mesh:

Year:  2016        PMID: 27603147     DOI: 10.1002/cncr.30326

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


  6 in total

1.  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
Journal:  Support Care Cancer       Date:  2018-03-29       Impact factor: 3.603

2.  Perceptions of care coordination in cancer patient-family caregiver dyads.

Authors:  Izumi Okado; Ian Pagano; Kevin Cassel; Randall F Holcombe
Journal:  Support Care Cancer       Date:  2020-09-24       Impact factor: 3.603

3.  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

4.  Cross-Cultural Adaptation And Pilot Testing Of The Cancer Care Coordination Questionnaire For Patients (CCCQ-P) In Chinese And Arabic Languages.

Authors:  Jane M Young; Rebecca L Venchiarutti; Ivana Durcinoska; Daniel Steffens
Journal:  Patient Prefer Adherence       Date:  2019-10-23       Impact factor: 2.711

5.  Patterns of follow up and survivorship care for people with colorectal cancer in new South Wales, Australia: a population-based survey.

Authors:  Jane M Young; Ivana Durcinoska; Katie DeLoyde; Michael J Solomon
Journal:  BMC Cancer       Date:  2018-03-27       Impact factor: 4.430

6.  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

  6 in total

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