Literature DB >> 21368682

Health Insurance Portability and Accountability Act (HIPAA) authorization and survey nonresponse bias.

Timothy J Beebe1, Jeanette Y Ziegenfuss, Jennifer L St Sauver, Sarah M Jenkins, Lindsey Haas, Michael E Davern, Nicholas J Talley.   

Abstract

OBJECTIVES: To extend earlier work (Beebe et al, Med Care. 2007;45:959-965) that demonstrated Health Insurance Portability and Accountability Act authorization form (HAF) introduced potential nonresponse bias (toward healthier respondents). RESEARCH
DESIGN: The sample frame from the earlier experiment was linked to administrative medical record data, enabling the comparison of background and clinical characteristics of each set of respondents (HAF and No HAF) to the sample frame.
SUBJECTS: A total of 6939 individuals residing in Olmsted County, Minnesota who were mailed a survey in September 2005 assessing recent gastrointestinal symptoms with an embedded HAF experiment comprised the study population. MEASURES: The outcomes of interest were response status (survey returned vs. not) by HAF condition (randomized to receive HAF or not). Sociodemographic indicators included gender, age, and race. Health status was measured using the severity-weighted Charlson Score and utilization was measured using emergency room visits, hospital admissions, clinic office visits, and procedures.
RESULTS: Younger and nonwhite residents were under-represented and those with more clinical office visits were over-represented in both conditions. Those responding to the survey in the HAF condition were significantly more likely to be in poor health compared with the population (27.3% with 2+ comorbidities vs. 24.6%, P=0.02).
CONCLUSIONS: The HAF did not influence the demographic composition of the respondents. However, in contrast to earlier findings based on self-reported health status (Beebe et al, Med Care. 2007;45:959-965), responders in the HAF condition were slightly sicker than in the non-HAF condition. The HAF may introduce a small amount of measurement error by suppressing reports of poor health. Furthermore, researchers should consider the effect of the HAF on resultant precision, respondent burden, and available financial resources.

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Mesh:

Year:  2011        PMID: 21368682      PMCID: PMC3179247          DOI: 10.1097/MLR.0b013e318202ada0

Source DB:  PubMed          Journal:  Med Care        ISSN: 0025-7079            Impact factor:   2.983


  18 in total

1.  Consequences of reducing nonresponse in a national telephone survey.

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2.  Potential effect of authorization bias on medical record research.

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Authors:  Maureen Murdoch; Diane M Pietila; Melissa R Partin
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Review 4.  The Health Insurance Portability and Accountability Act of 1996 (HIPAA) privacy rule: implications for clinical research.

Authors:  Rachel Nosowsky; Thomas J Giordano
Journal:  Annu Rev Med       Date:  2006       Impact factor: 13.739

5.  The HIPAA authorization form and effects on survey response rates, nonresponse bias, and data quality: a randomized community study.

Authors:  Timothy J Beebe; Nicholas J Talley; Michael Camilleri; Sarah M Jenkins; Kari J Anderson; G Richard Locke
Journal:  Med Care       Date:  2007-10       Impact factor: 2.983

6.  The impact of HIPAA authorization on willingness to participate in clinical research.

Authors:  Anne L Dunlop; Tracie Graham; Zanie Leroy; Karen Glanz; Boadie Dunlop
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9.  Potential impact of the HIPAA privacy rule on data collection in a registry of patients with acute coronary syndrome.

Authors:  David Armstrong; Eva Kline-Rogers; Sandeep M Jani; Edward B Goldman; Jianming Fang; Debabrata Mukherjee; Brahmajee K Nallamothu; Kim A Eagle
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10.  Randomized trial showed requesting medical records with a survey produced a more representative sample than requesting separately.

Authors:  Melissa R Partin; Diana J Burgess; Krysten Halek; Joseph Grill; Sally W Vernon; Deborah A Fisher; Joan M Griffin; Maureen Murdoch
Journal:  J Clin Epidemiol       Date:  2008-06-11       Impact factor: 6.437

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  7 in total

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Authors:  Timothy J Beebe; Jeanette Y Ziegenfuss; Sarah M Jenkins; Lindsey R Haas; Michael E Davern
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2.  Evaluating survey quality in health services research: a decision framework for assessing nonresponse bias.

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5.  Use of a medical records linkage system to enumerate a dynamic population over time: the Rochester epidemiology project.

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6.  Deployment of a mixed-mode data collection strategy does not reduce nonresponse bias in a general population health survey.

Authors:  Timothy J Beebe; Donna D McAlpine; Jeanette Y Ziegenfuss; Sarah Jenkins; Lindsey Haas; Michael E Davern
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Review 7.  Harmonizing and consolidating the measurement of patient-reported information at health care institutions: a position statement of the Mayo Clinic.

Authors:  David T Eton; Timothy J Beebe; Philip T Hagen; Michele Y Halyard; Victor M Montori; James M Naessens; Jeff A Sloan; Carrie A Thompson; Douglas L Wood
Journal:  Patient Relat Outcome Meas       Date:  2014-02-10
  7 in total

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