Results and their implications from comparing respondents and proxy responses for non-respondents with cognitive difficulties on a telephone survey

Mary Adams, M.S., M.P.H.

Disability and Health Journal, January 2017,
DOI: http://dx.doi.org/10.1016/j.dhjo.2016.09.004

 

Background

Limited study has been done on proxy responses for non-respondents with subjective cognitive decline (SCD) on the Behavioral Risk Factor Surveillance System (BRFSS).

Objective

To directly compare results for survey respondents with SCD with those for proxies provided for non-respondents with SCD.

Methods

Publicly available 2011 BRFSS data from 120,485 households in 21 states were analyzed using Stata. Respondents ages 40 and older with SCD (n = 10,831) were compared with proxy responses for non-respondents ages 40 and older with SCD (n = 4296) living in households where the respondent did not have SCD. Outcome measures included functional difficulties associated with their SCD, needing help, receiving informal care, talking with a healthcare provider about their SCD, getting treatment, and having a dementia diagnosis. Logistic regression for each outcome controlled for age, household income, state of residence, and number of household adults.

Results

Non-respondents were significantly more likely than respondents by Pearson chi square tests with alpha = 0.05 to report all 6 outcomes. Adjusted odds ratios comparing non-respondents with respondents ranged from 2.61 (95% confidence interval: 2.22–3.07) for needing help, to 8.99 (6.60–12.24) for a dementia diagnosis and confirmed unadjusted results.

Conclusion

Respondent results only represent adults capable of answering a telephone survey. To represent all household adults and avoid nonresponse bias that may under-represent the true population parameters by as much as 70%, results must include both respondents and non-respondents. Other measures may be similarly affected if they inhibit one’s ability to respond to a telephone survey (e.g. disability, stroke).