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Estimated odds ratio for dropping out of the study at T3 and T4 given status at prior visit.
The estimated Odds Ratio for dropping out of the study given failure to achieve remission at the prior visit is 7.3 for T3 (95% Confidence Interval: 4.7 11.2) and 8.8 at T4 for subjects not in remission at prior visit (95% Confidence Interval: 5.6 13.9).
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The dosage and timing of insulin recommended at prior visits was often not being used, and perhaps had never been attempted.
Logistic regression models were fit in order to calculate the likelihood of maintaining remission based on status at prior visits (see Table 7).
If a BMI measurement was not obtained at a visit, the measurement obtained at the prior visit (if within 9 months) was used.
This visual impression was statistically confirmed in a transition analysis that evaluated whether the odds of a positive oral HPV test at a given visit was affected by the HPV viral load at the prior visit (Table 4).
For HIV-1 seropositive women, a separate model was constructed which included CD4+ count and HAART use at the prior visit and maximum viral load during the study period.
The system also allowed us to record whether or not the specific product container had been seen at a prior visit, allowing us to track specific containers and their use over time.
In men who used nPEP at the prior visit, there were elevated odds of reporting SDUA compared to those who didn't previously use nPEP (aOR: 1.6, [95%CI: 1.2, 2.1], Table 4).
While patients typically are prescribed 30 days of ART medication at each visit, the actual amount of medication dispensed ranged above and below this value; the refill date was calculated based on the amount of medication given to the patient at the prior visit.
The model among HIV-1 seropositive women indicated a trend towards a protective effect for increasing CD4+ count at the prior visit (aHR 0.79 for each 100 cells/μL increase, 95%CI: 0.61 to 1.02, P = 0.07), but the use of HAART per se was not protective.
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