Literature DB >> 9834771

The impact of requiring patient authorization for use of data in medical records research.

B P Yawn1, R A Yawn, G R Geier, Z Xia, S J Jacobsen.   

Abstract

BACKGROUND: In 1996, the Minnesota legislature passed a medical data privacy act requiring patient authorization for the use of medical records in research. Other state legislatures and Congress are considering similar legislation. The impact of this statute on a researcher's ability to obtain complete and representative data is unknown.
METHODS: This was a cross-sectional study of all patients visiting the outpatient clinic, emergency department, or hospital of the Olmsted Medical Center (OMC), for an appointment or admission during January 1997 or February 1997. Patients were asked to give consent for the use of their medical records for research. Our objective was to gather information on the number and characteristics of patients who refused authorization.
RESULTS: Of the 15,997 patients: 90.6% granted authorization; 3.6 refused authorization; 4.5% were undecided; and 1.3% were not asked for authorization. Refusal rates were highest among patients visiting the center for mental health concerns, trauma, or eye care, and among women aged 39 years or older. Undecided rates were highest in women presenting for pregnancy care.
CONCLUSIONS: Refusal rates were low for this community practice. However, higher refusal rates in some subgroups, such as older women or patients with mental health concerns, may increase the chance of selection bias in studies involving these patients.

Entities:  

Keywords:  Biomedical and Behavioral Research; Empirical Approach; Professional Patient Relationship

Mesh:

Year:  1998        PMID: 9834771

Source DB:  PubMed          Journal:  J Fam Pract        ISSN: 0094-3509            Impact factor:   0.493


  49 in total

1.  The privacy paradox: laying Orwell's ghost to rest.

Authors:  R E Upshur; B Morin; V Goel
Journal:  CMAJ       Date:  2001-08-07       Impact factor: 8.262

2.  The use of medical records in research: what do patients want?

Authors:  Nancy E Kass; Marvin R Natowicz; Sara Chandros Hull; Ruth R Faden; Laura Plantinga; Lawrence O Gostin; Julia Slutsman
Journal:  J Law Med Ethics       Date:  2003       Impact factor: 1.718

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Authors:  Maureen Murdoch; Diane M Pietila; Melissa R Partin
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4.  Risk of herpes zoster in children with asthma.

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5.  Who doesn't authorize the linking of survey and administrative health data? A general population-based investigation.

Authors:  Timothy J Beebe; Jeanette Y Ziegenfuss; Sarah M Jenkins; Lindsey R Haas; Michael E Davern
Journal:  Ann Epidemiol       Date:  2011-04-16       Impact factor: 3.797

6.  Ethical and practical challenges to studying patients who opt out of large-scale biorepository research.

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Journal:  J Am Med Inform Assoc       Date:  2013-07-25       Impact factor: 4.497

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8.  Changing Incidence of Serum 25-Hydroxyvitamin D Values Above 50 ng/mL: A 10-Year Population-Based Study.

Authors:  Daniel V Dudenkov; Barbara P Yawn; Sara S Oberhelman; Philip R Fischer; Ravinder J Singh; Stephen S Cha; Julie A Maxson; Stephanie M Quigg; Tom D Thacher
Journal:  Mayo Clin Proc       Date:  2015-05       Impact factor: 7.616

9.  Personal privacy and public health: potential impacts of privacy legislation on health research in Canada.

Authors:  M Anne Harris; Adrian R Levy; Kay E Teschke
Journal:  Can J Public Health       Date:  2008 Jul-Aug

10.  The effect of privacy legislation on observational research.

Authors:  Andrea S Gershon; Jack V Tu
Journal:  CMAJ       Date:  2008-03-25       Impact factor: 8.262

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