Literature DB >> 22267819

Use of electronic documentation for quality improvement in hospice.

John G Cagle1, Franziska S Rokoske, Danielle Durham, Anna P Schenck, Carol Spence, Laura C Hanson.   

Abstract

Little evidence exists about the use of electronic documentation (ED) in hospice and its relationship to quality improvement (QI) practices. The purposes of this study were to (1) estimate the prevalence of ED use in hospice, (2) identify organizational characteristics associated with use of ED, and (3) determine whether quality measurement practices differed based on documentation format (electronic vs nonelectronic). Surveys concerning the use of ED for QI practices and the monitoring of quality-related care and outcomes were collected from 653 hospices. Users of ED were able to monitor a wider range of quality-related data than users of non-ED. Quality components such as advanced care planning, cultural needs, experience during care of the actively dying, and the number/types of care being delivered were more likely to be documented by users of ED. Use of ED may help hospices monitor quality and compliance.

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Year:  2012        PMID: 22267819      PMCID: PMC4405247          DOI: 10.1177/1062860611425103

Source DB:  PubMed          Journal:  Am J Med Qual        ISSN: 1062-8606            Impact factor:   1.852


  22 in total

1.  Hospices' preparation and practices for quality measurement.

Authors:  Laura C Hanson; Anna P Schenck; Franziska S Rokoske; Amy P Abernethy; Jean S Kutner; Carol Spence; Judi Lund Person
Journal:  J Pain Symptom Manage       Date:  2010-01       Impact factor: 3.612

2.  Family evaluation of hospice care: results from voluntary submission of data via website.

Authors:  Stephen R Connor; Joan Teno; Carol Spence; Neal Smith
Journal:  J Pain Symptom Manage       Date:  2005-07       Impact factor: 3.612

3.  Barriers to the adoption of electronic health records: using concept mapping to develop a comprehensive empirical model.

Authors:  Arun Vishwanath; Susan D Scamurra
Journal:  Health Informatics J       Date:  2007-06       Impact factor: 2.681

Review 4.  The national agenda for quality palliative care: the National Consensus Project and the National Quality Forum.

Authors:  Betty Ferrell; Stephen R Connor; Anne Cordes; Constance M Dahlin; Perry G Fine; Nancy Hutton; Mark Leenay; Judy Lentz; Judi Lund Person; Diane E Meier; Ken Zuroski
Journal:  J Pain Symptom Manage       Date:  2007-06       Impact factor: 3.612

5.  A point of care clinical documentation system for hospice care providers.

Authors:  Kyusuk Chung; Ralph Bell; Dennis Lee
Journal:  J Med Syst       Date:  2006-02       Impact factor: 4.460

6.  Coordinating care--a perilous journey through the health care system.

Authors:  Thomas Bodenheimer
Journal:  N Engl J Med       Date:  2008-03-06       Impact factor: 91.245

7.  Factors affecting electronic health record adoption in long-term care facilities.

Authors:  Barbara Cherry; Michael Carter; Donna Owen; Carol Lockhart
Journal:  J Healthc Qual       Date:  2008 Mar-Apr       Impact factor: 1.095

8.  A system of electronic records developed by a children's hospice.

Authors:  Antoinette Menezes; Polly Esplen; Paul Bartlett; Bridget Turner; Mike Keel; Veronica Etherington; Elaine Conisbee; Antonia Plant; Val Haslam; Julie England
Journal:  Int J Palliat Nurs       Date:  2007-05

9.  Medicare and Medicaid programs: hospice conditions of participation. Final rule.

Authors: 
Journal:  Fed Regist       Date:  2008-06-05

10.  Employing the electronic health record to improve diabetes care: a multifaceted intervention in an integrated delivery system.

Authors:  Valerie Weber; Frederick Bloom; Steve Pierdon; Craig Wood
Journal:  J Gen Intern Med       Date:  2008-04       Impact factor: 5.128

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  1 in total

1.  Clinical documentation: composition or synthesis?

Authors:  Lena Mamykina; David K Vawdrey; Peter D Stetson; Kai Zheng; George Hripcsak
Journal:  J Am Med Inform Assoc       Date:  2012-07-19       Impact factor: 4.497

  1 in total

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