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They found that functional outcome, as measured by the FOSQ, for patients in the home testing group was not clinically inferior to usual laboratory-based testing when using an a priori non-inferiority margin of ?1.0 for the difference in mean change in FOSQ score at 3 months (home mean change of 1.74 vs laboratory mean change of 1.85, adjusted difference 0.0, [http://www.selleckchem.com/products/Dasatinib.html Dasatinib ic50] lower bound of one-sided 95% confidence interval ?0.54). They found that CPAP adherence in the home testing group was also not inferior to the laboratory-based testing group, with mean?��?standard deviation daily use of 3.5?��?2.5?h versus 2.9?��?2.3?h, respectively, using an a priori non-inferiority margin of ?0.75?h (adjusted difference 0.55, lower bound of one-sided 95% confidence interval 0.03). Furthermore, there were no statistically significant differences in the change in ESS score, psychomotor vigilance, health outcomes as measured by the short form-12 health survey or depression scale scores between the two groups. More recently, Rosen et?al. conducted a multisite, randomized study comparing home-based, unattended, level [http://en.wikipedia.org/wiki/Oxygenase Oxygenase] 3 monitoring and autotitrating CPAP with in-laboratory PSG and CPAP titration for a total of 3 months of follow up.[69] Participants randomized had a high pretest probability of moderate-to-severe OSA, identified by a clinical algorithm (i.e. ��adjusted neck circumference�� ?43?cm) and ESS ��12, [http://www.selleckchem.com/products/Gefitinib.html Gefitinib order] and were eligible to continue in the study if found by portable monitoring or laboratory PSG to have an AHI ��15/h. Patients in the home-based arm who were found on portable monitoring to have an AHI

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Cloth59butter : Page créée avec « They found that functional outcome, as measured by the FOSQ, for patients in the home testing group was not clinically inferior to usual laboratory-based testing when usin... »