Posted on: 13 February 2014 By: jkrieger

Pre/post evaluation designs of asthma interventions are weak since absent any intevention, utilization decreases over time due to regression to mean. Convincing (at least to researchers) studies require a control group. Are the pre/post data sufficient to convince plans, medicaid officials, etc. of the value proposition?

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BrendaDoroski


Thu, 02/13/2014 - 15:21

This is a great question.  We're going to contact a few health plan Network members to respond to this question.  Stay tuned!

floydmalveaux


Thu, 02/13/2014 - 15:24

As you know, we struggle with this issue in our work at MCAN.  Would be interested to hear from health plans on this, but we should also look to a recent article by Ko et.al "Declines with Age in Childhood Asthma Symptoms and Health Care Use. An Adjustment for Evaluations",http://www.atsjournals.org/doi/abs/10.1513/AnnalsATS.201304-093OC#.Uv0o…

You may recall that Noreen Clark was working with biostatisticians to develop a statistical method to account for the natural decline in symptoms we see among children with asthma as they age.  This method can be a very useful tool for studies in which a control group is not feasible, i.e. pre/post studies.  The method "clones" a control group, using existing data, to compare against the intervention group.

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