Capture, Transfer, and Feedback of Patient-Centered Outcomes Data in Palliative Care Populations: Does It Make a Difference? A Systematic Review
Autor: | Irene J Higginson, Jana Witt, Fliss E M Murtagh, Wingfai Kwok, Simon Noah Etkind, Barbara A Daveson, Claudia Bausewein |
---|---|
Přispěvatelé: | Etkind, Simon [0000-0003-2863-8893], Apollo - University of Cambridge Repository |
Jazyk: | angličtina |
Předmět: |
medicine.medical_specialty
Palliative care data collection Feedback Psychological MEDLINE Nursing(all) Clinical Neurology review Context (language use) CINAHL PsycINFO Quality of life (healthcare) Nursing Outcome Assessment Health Care medicine Humans Outcome assessment (health care) General Nursing palliative care business.industry Communication Patient-centered outcomes Professional-Patient Relations Hospice and palliative medicine Anesthesiology and Pain Medicine quality of life Family medicine hospice care Neurology (clinical) business |
Zdroj: | Etkind, S N, Daveson, B A, Kwok, W, Witt, J, Bausewein, C, Higginson, I J & Murtagh, F E M 2015, ' Capture, Transfer, and Feedback of Patient-Centered Outcomes Data in Palliative Care Populations : Does It Make a Difference? A Systematic Review ', Journal of pain and symptom management, vol. 49, no. 3, pp. 611-624 . https://doi.org/10.1016/j.jpainsymman.2014.07.010 |
ISSN: | 0885-3924 |
DOI: | 10.1016/j.jpainsymman.2014.07.010 |
Popis: | Context. Patient-centered outcome measures (PCOMs) are an important way of promoting patient-professional communication. However, evidence regarding their implementation in palliative care is limited, as is evidence of the impact on care quality and outcomes. Objectives. The aim was to systematically review evidence on capture and feedback of PCOMs in palliative care populations and determine the effects on processes and outcomes of care. Methods. We searched Medline, Embase, CINAHL, BNI, PsycINFO, and gray literature from 1985 to October 2013 for peer-reviewed articles focusing on collection, transfer, and feedback of PCOMs in palliative care populations. Two researchers independently reviewed all included articles. Review articles, feasibility studies, and those not measuring PCOMs in clinical practice were excluded. We quality assessed articles using modified Edwards criteria and undertook narrative synthesis. Results. One hundred eighty-four articles used 122 different PCOMs in 70,466 patients. Of these, 16 articles corresponding to 13 studies met the full inclusion criteria. Most evidence was from outpatient oncology. There was strong evidence for an impact of PCOMs feedback on processes of care including better symptom recognition, more discussion of quality of life, and increased referrals based on PCOMs reporting. There was evidence of improved emotional and psychological patient outcomes but no effect on overall quality of life or symptom burden. Conclusion. Inpalliativecarepopulations,PCOMsfeedbackimprovesawarenessofunmetneedandallowsprofessionalstoact to address patients’ needs. It consequently benefits patients’ emotional and psychological quality of life. However, more highquality evidence is needed in noncancer populations and across a wider range of settings. J Pain Symptom Manage 2015;49:611e624. 2015 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. |
Databáze: | OpenAIRE |
Externí odkaz: |