Literature DB >> 22045369

Collecting data on quality is feasible in community-based palliative care.

Arif H Kamal1, Janet Bull, Charles Stinson, Debra Blue, Robert Smith, Rikki Hooper, Melanie Kelly, Judith Kinsella, Mark Philbrick, Agbessi Gblokpor, Jane L Wheeler, William Downey, Amy P Abernethy.   

Abstract

BACKGROUND: Quality measurement in palliative care requires robust data from standardized data collection processes. We developed and tested the feasibility of the Quality Data Collection Tool version 1.0 (QDACTv1.0) for use in community-based palliative care. MEASURES: To evaluate for implementation barriers, we tested feasibility, acceptability, and utility of the QDACTv1.0 by reviewing use patterns, surveying clinician users, and reporting conformance with quality metrics. INTERVENTION: Comprising 37 questions within five domains, QDACTv1.0 was launched in May 2008 for data collection at point of care. OUTCOMES: Through March 2011, data on 5959 patients in 19,734 visits have been collected. We observed steady quarterly growth in data collection, positive clinician feedback, and successful mapping of data to quality metrics. Information gathered characterized practice variations and suggested quality improvement initiatives. Clinician feedback has driven updating to Quality Data Collection Tool version 2.0. CONCLUSIONS/LESSONS LEARNED: Standardized data collection is feasible in routine community-based palliative care and is valuable for quality monitoring. Copyright Â
© 2011 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 22045369     DOI: 10.1016/j.jpainsymman.2011.07.003

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  8 in total

1.  Development of the Quality Data Collection Tool for Prospective Quality Assessment and Reporting in Palliative Care.

Authors:  Arif H Kamal; Janet Bull; Dio Kavalieratos; Jonathan M Nicolla; Laura Roe; Martha Adams; Amy P Abernethy
Journal:  J Palliat Med       Date:  2016-06-27       Impact factor: 2.947

2.  Usability and Acceptability of the QDACT-PC, an Electronic Point-of-Care System for Standardized Quality Monitoring in Palliative Care.

Authors:  Arif H Kamal; Dio Kavalieratos; Janet Bull; Charles S Stinson; Jonathan Nicolla; Amy P Abernethy
Journal:  J Pain Symptom Manage       Date:  2015-07-10       Impact factor: 3.612

3.  Determinants of longitudinal health-related quality-of-life change in children with asthma from low-income families: a report from the PROMIS® Pediatric Asthma Study.

Authors:  Z Li; W L Leite; L A Thompson; H E Gross; E A Shenkman; B B Reeve; D A DeWalt; I-C Huang
Journal:  Clin Exp Allergy       Date:  2016-10-21       Impact factor: 5.018

Review 4.  Improving the Quality of Palliative Care Through National and Regional Collaboration Efforts.

Authors:  Arif H Kamal; Krista L Harrison; Marie Bakitas; J Nicholas Dionne-Odom; Lisa Zubkoff; Imatullah Akyar; Steven Z Pantilat; David L O'Riordan; Ashley R Bragg; Kara E Bischoff; Janet Bull
Journal:  Cancer Control       Date:  2015-10       Impact factor: 3.302

5.  Quality of palliative care for patients with advanced cancer in a community consortium.

Authors:  Arif H Kamal; Ryan D Nipp; Janet H Bull; Charles S Stinson; Ashlei W Lowery; Jonathan M Nicolla; Amy P Abernethy
Journal:  J Pain Symptom Manage       Date:  2014-09-08       Impact factor: 3.612

6.  Conformance with supportive care quality measures is associated with better quality of life in patients with cancer receiving palliative care.

Authors:  Arif H Kamal; Janet Bull; Charles S Stinson; Debra L Blue; Amy P Abernethy
Journal:  J Oncol Pract       Date:  2013-05       Impact factor: 3.840

7.  Improving national hospice/palliative care service symptom outcomes systematically through point-of-care data collection, structured feedback and benchmarking.

Authors:  David C Currow; Samuel Allingham; Patsy Yates; Claire Johnson; Katherine Clark; Kathy Eagar
Journal:  Support Care Cancer       Date:  2014-07-27       Impact factor: 3.603

8.  Case Studies from the Clinic: Initiating and Implementing Patient-Reported Outcome Measures.

Authors:  Tracie Locklear; Lynn L DeBar; James Willig; Sean Rundell; Leslie Blackhall; Douglas Zatzick; Karen Staman; Nrupen Bhavsar; Kevin Weinfurt; Amy P Abernethy
Journal:  EGEMS (Wash DC)       Date:  2017-06-12
  8 in total

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