2019
DOI: 10.1002/cpp.2364
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Bias through selective inclusion and attrition: Representativeness when comparing provider performance with routine outcome monitoring data

Abstract: Background Observational research based on routine outcome monitoring is prone to missing data, and outcomes can be biased due to selective inclusion at baseline or selective attrition at posttest. As patients with complete data may not be representative of all patients of a provider, missing data may bias results, especially when missingness is not random but systematic. Methods The present study establishes clinical and demographic patient variables relevant for representativeness of the outcome information.… Show more

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Cited by 14 publications
(9 citation statements)
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References 37 publications
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“…In addition, efforts to ensure patients complete treatment may be more limited in effectiveness studies than in efficacy studies (Byrne et al, 2011). In addition, as more than 50% of all patients showed compliance regarding the assessments, the results can be generalised to other eating disorder patients (de Beurs et al, 2019). Motivational sessions prior to commencing treatment might reduce drop-out and enhance treatment completion among patients suffering from BN.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, efforts to ensure patients complete treatment may be more limited in effectiveness studies than in efficacy studies (Byrne et al, 2011). In addition, as more than 50% of all patients showed compliance regarding the assessments, the results can be generalised to other eating disorder patients (de Beurs et al, 2019). Motivational sessions prior to commencing treatment might reduce drop-out and enhance treatment completion among patients suffering from BN.…”
Section: Discussionmentioning
confidence: 99%
“…A few studies have examined ROM implementation report data on engagement and attrition rates [ 8 , 25 , 28 , 110 , 111 ]. Compared with recent data from the Netherlands, however, the proportion of participants using SMART Track to input ROM data is largely comparable, and in some cases, greater than traditional clinician-completed methods [ 112 ]. A 50% response rate has been recently suggested as an acceptable benchmark for ROM data and is likely sufficient to protect against bias and yield valid information about patient progress (see study by de Beurs et al [ 112 ] for a discussion).…”
Section: Discussionmentioning
confidence: 99%
“…Compared with recent data from the Netherlands, however, the proportion of participants using SMART Track to input ROM data is largely comparable, and in some cases, greater than traditional clinician-completed methods [ 112 ]. A 50% response rate has been recently suggested as an acceptable benchmark for ROM data and is likely sufficient to protect against bias and yield valid information about patient progress (see study by de Beurs et al [ 112 ] for a discussion). In this study, this benchmark was achieved each week across the first month of data collection, with 83% (60/72), 63% (45/72), 60% (43/72), and 53% (38/72) of the study participants completing at least one of the ROM instruments across the first 4 weeks of app use.…”
Section: Discussionmentioning
confidence: 99%
“…Only treatments with complete pretest and post‐test data for the first year were included, about 55% of all treatments that had been started, 43.8% of the S‐MHC and 70.3% of the B‐MHC treatments. We compared fully assessed treatments to treatments with incomplete data on pretest patient characteristics to check for selective ROM non‐response (de Beurs, Warmerdam, & Twisk, 2019 ).…”
Section: Methodsmentioning
confidence: 99%