Co-enrollment of critically ill patients into multiple studies: patterns, predictors and consequences
| dc.contributor.author | Cook, Deborah | |
| dc.contributor.author | McDonald, Ellen | |
| dc.contributor.author | Smith, Orla | |
| dc.contributor.author | Zytaruk, Nicole | |
| dc.contributor.author | Heels-Ansdell, Diane | |
| dc.contributor.author | Watpool, Irene | |
| dc.contributor.author | McArdle, Tracy | |
| dc.contributor.author | Matte, Andrea | |
| dc.contributor.author | Clarke, France | |
| dc.contributor.author | Vallance, Shirley | |
| dc.contributor.author | Finfer, Simon | |
| dc.contributor.author | Galt, Pauline | |
| dc.contributor.author | Crozier, Tim | |
| dc.contributor.author | Fowler, Rob | |
| dc.contributor.author | Arabi, Yaseen | |
| dc.contributor.author | Woolfe, Clive | |
| dc.contributor.author | Orford, Neil | |
| dc.contributor.author | Hall, Richard | |
| dc.contributor.author | Adhikari, Neill K | |
| dc.contributor.author | Ferland, Marie-Clauide | |
| dc.contributor.author | Marshall, John | |
| dc.contributor.author | Meade, Maureen | |
| dc.date.accessioned | 2015-12-18T10:58:13Z | |
| dc.date.available | 2015-12-18T10:58:13Z | |
| dc.date.issued | 2013-01-08 | |
| dc.date.updated | 2015-12-18T10:58:13Z | |
| dc.description.abstract | Abstract Introduction Research on co-enrollment practices and their impact are limited in the ICU setting. The objectives of this study were: 1) to describe patterns and predictors of co-enrollment of patients in a thromboprophylaxis trial, and 2) to examine the consequences of co-enrollment on clinical and trial outcomes. Methods In an observational analysis of an international thromboprophylaxis trial in 67 ICUs, we examined the co-enrollment of critically ill medical-surgical patients into more than one study, and examined the clinical and trial outcomes among co-enrolled and non-co-enrolled patients. Results Among 3,746 patients enrolled in PROTECT (Prophylaxis for ThromboEmbolism in Critical Care Trial), 713 (19.0%) were co-enrolled in at least one other study (53.6% in a randomized trial, 37.0% in an observational study and 9.4% in both). Six factors independently associated with co-enrollment (all P < 0.001) were illness severity (odds ratio (OR) 1.35, 95% confidence interval (CI) 1.19 to 1.53 for each 10-point Acute Physiology and Chronic Health Evaluation (APACHE) II score increase), substitute decision-makers providing consent, rather than patients (OR 3.31, 2.03 to 5.41), experience of persons inviting consent (OR 2.67, 1.74 to 4.11 for persons with > 10 years' experience compared to persons with none), center size (all ORs > 10 for ICUs with > 15 beds), affiliation with trials groups (OR 5.59, 3.49 to 8.95), and main trial rather than pilot phase (all ORs > 8 for recruitment year beyond the pilot). Co-enrollment did not influence clinical or trial outcomes or risk of adverse events. Conclusions Co-enrollment was strongly associated with features of the patients, research personnel, setting and study. Co-enrollment had no impact on trial results, and appeared safe, acceptable and feasible. Transparent reporting, scholarly discourse, ethical analysis and further research are needed on the complex topic of co-enrollment during critical illness. | |
| dc.identifier.citation | Critical Care. 2013 Jan 08;17(1):R1 | |
| dc.identifier.uri | http://dx.doi.org/10.1186/cc11917 | |
| dc.identifier.uri | http://hdl.handle.net/10393/33953 | |
| dc.language.rfc3066 | en | |
| dc.rights.holder | Cook et al.; licensee BioMed Central Ltd. | |
| dc.title | Co-enrollment of critically ill patients into multiple studies: patterns, predictors and consequences | |
| dc.type | Journal Article |
