Patient-Reported Experiences and Associated Factors in a Norwegian Radiotherapy Setting: An Explorative Cross-Sectional Study.
| Autor: | Volungholen Sollid, May Ingvild, Slaaen, Marit, Danielsen, Signe, Eilertsen, Grethe, Kirkevold, Øyvind |
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| Předmět: |
MEDICAL quality control
RESEARCH CANCER patient psychology MATHEMATICAL statistics SPECIALTY hospitals PARAMETERS (Statistics) CROSS-sectional method SELF-evaluation MEDICAL care HEALTH outcome assessment REGRESSION analysis PATIENT-centered care PATIENTS' attitudes EXPERIENCE CANCER treatment PEARSON correlation (Statistics) T-test (Statistics) QUESTIONNAIRES DESCRIPTIVE statistics INTERPROFESSIONAL relations CHI-squared test RESEARCH funding TUMORS DATA analysis software |
| Zdroj: | SAGE Open Nursing; 2/21/2024, p1-13, 13p |
| Abstrakt: | Introduction: Radiotherapy is the main treatment modality in cancer. There is sparse knowledge on how patients with cancer experience their radiotherapy trajectory, and which factors might be associated with patients' experiences. Objectives: The aim of the present study was to explore how adults with cancer receiving radiotherapy evaluate the quality of their care, utilizing a patient-reported experience measure, and how patient- and service-related characteristics are associated with their evaluation. Methods: An explorative cross-sectional study using a self-completed questionnaire to assess patients' radiotherapy experiences was performed. Participants were recruited consecutively, within their last week of treatment, from two different hospitals in Norway from January 2021 to January 2022. Four hundred and eighty paper questionnaires were distributed to recruited patients, 240 at each hospital. Questionnaires were self-completed at home and returned by mail. The instrument person-centered coordinated care experience questionnaire (P3CEQ) was used. In addition to this, participants completed the European Organization of Research and Treatment of Cancer Quality of Life Questionnaire-C30 (EORTC QLQ-C30) and The Sense of Coherence 13 scale (SOC-13). Data were analyzed using descriptive statistics, parametric tests, and unadjusted/adjusted linear regression models were estimated. Results: The study included 373 patients. Patients evaluated quality of care in terms of P3CEQ scores, with a mean score of 19.5 (standard deviation = 5.4). Lowest scores were identified in areas concerning person-centeredness and service coordination. There were no significant differences in P3CEQ scores between the younger and older groups. Having a partner and better SOC-13 scores were independently associated with the overall patient-reported experience score, whereas age was not. Conclusion: Patient-reported experience scores indicate that improvements are needed in some areas, such as informing and involving patients in the planning and coordination of their care. Findings suggest paying special attention to patients without a partner to offer patients the best possible care. [ABSTRACT FROM AUTHOR] |
| Databáze: | Complementary Index |
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