Literature DB >> 31413986

Patient-Centered Outcomes Measurement: Does It Require Information From Patients?

Leif I Solberg1, Stephen E Asche1, John Butler2, David Carrell3, Christine K Norton4, Jeffrey G Jarvik5, Rebecca Smith-Bindman6, Juliana O Tillema1, Robin R Whitebird7, Ann M Werner1, Jeanette Y Ziegenfuss1.   

Abstract

PURPOSE: Since collecting outcome measure data from patients can be expensive, time-consuming, and subject to memory and nonresponse bias, we sought to learn whether outcomes important to patients can be obtained from data in the electronic health record (EHR) or health insurance claims.
METHODS: We previously identified 21 outcomes rated important by patients who had advanced imaging tests for back or abdominal pain. Telephone surveys about experiencing those outcomes 1 year after their test from 321 people consenting to use of their medical record and claims data were compared with audits of the participants' EHR progress notes over the time period between the imaging test and survey completion. We also compared survey data with algorithmically extracted data from claims files for outcomes for which data might be available from that source.
RESULTS: Of the 16 outcomes for which patients' survey responses were considered to be the best information source, only 2 outcomes for back pain and 3 for abdominal pain had kappa scores above a very modest level of ≥ 0.2 for chart audit of EHR data and none for algorithmically obtained EHR/claims data. Of the other 5 outcomes for which claims data were considered to be the best information source, only 2 outcomes from patient surveys and 3 outcomes from chart audits had kappa scores ≥ 0.2.
CONCLUSIONS: For the types of outcomes studied here, medical record or claims data do not provide an adequate source of information except for a few outcomes where patient reports may be less accurate.

Entities:  

Keywords:  electronic health records; patient-centered care; patient-reported outcomes

Year:  2017        PMID: 31413986      PMCID: PMC6664353          DOI: 10.17294/2330-0698.1456

Source DB:  PubMed          Journal:  J Patient Cent Res Rev        ISSN: 2330-068X


  24 in total

1.  Evaluating the quality of self-reports of hypertension and diabetes.

Authors:  Noreen Goldman; I-Fen Lin; Maxine Weinstein; Yu-Hsuan Lin
Journal:  J Clin Epidemiol       Date:  2003-02       Impact factor: 6.437

2.  What is the concordance between the medical record and patient self-report as data sources for ambulatory care?

Authors:  Diana M Tisnado; John L Adams; Honghu Liu; Cheryl L Damberg; Wen-Pin Chen; Fang Ashlee Hu; David M Carlisle; Carol M Mangione; Katherine L Kahn
Journal:  Med Care       Date:  2006-02       Impact factor: 2.983

3.  Agreement between self-reported and health insurance claims on utilization of health care: A population study.

Authors:  Sheng-Tsung Yu; Hsing-Yi Chang; Ming-Chu Lin; Yu-Hsuan Lin
Journal:  J Clin Epidemiol       Date:  2009-04-28       Impact factor: 6.437

4.  The use of PROMIS and assessment center to deliver patient-reported outcome measures in clinical research.

Authors:  Richard C Gershon; Nan Rothrock; Rachel Hanrahan; Michael Bass; David Cella
Journal:  J Appl Meas       Date:  2010

5.  Agreement between patient reports of cardiovascular disease and patient medical records.

Authors:  Jennifer L St Sauver; Philip T Hagen; Stephen S Cha; Stephanie M Bagniewski; Jayawant N Mandrekar; Ann M Curoe; Richard J Rodeheffer; Veronique L Roger; Steven J Jacobsen
Journal:  Mayo Clin Proc       Date:  2005-02       Impact factor: 7.616

6.  Testing for prostate and colorectal cancer: comparison of self-report and medical record audit.

Authors:  H Irene Hall; Stephen K Van Den Eeden; Dennis D Tolsma; Kate Rardin; Trevor Thompson; Amber Hughes Sinclair; Diane J Madlon-Kay; Marion Nadel
Journal:  Prev Med       Date:  2004-07       Impact factor: 4.018

7.  Validity of self-reported mammography: examining recall and covariates among older women in a Health Maintenance Organization.

Authors:  Lee S Caplan; Margaret T Mandelson; Lynda A Anderson
Journal:  Am J Epidemiol       Date:  2003-02-01       Impact factor: 4.897

8.  How accurate are self-reports? Analysis of self-reported health care utilization and absence when compared with administrative data.

Authors:  Meghan E Short; Ron Z Goetzel; Xiaofei Pei; Maryam J Tabrizi; Ronald J Ozminkowski; Teresa B Gibson; Dave M Dejoy; Mark G Wilson
Journal:  J Occup Environ Med       Date:  2009-07       Impact factor: 2.162

9.  Good agreement between questionnaire and administrative databases for health care use and costs in patients with osteoarthritis.

Authors:  Daniel Pinto; M Clare Robertson; Paul Hansen; J Haxby Abbott
Journal:  BMC Med Res Methodol       Date:  2011-04-13       Impact factor: 4.615

10.  Development and first assessment of a questionnaire for health care utilization and costs for cardiac patients.

Authors:  Bernd Schweikert; Harry Hahmann; Reiner Leidl
Journal:  BMC Health Serv Res       Date:  2008-09-19       Impact factor: 2.655

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  1 in total

1.  What Outcomes Matter to Patients After Joint or Spine Surgery?

Authors:  Robin R Whitebird; Leif I Solberg; Christine K Norton; Jeanette Y Ziegenfuss; Stephen E Asche; Elizabeth S Grossman
Journal:  J Patient Cent Res Rev       Date:  2020-04-27
  1 in total

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