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Results: Differences in an interval version of the motor portion of the FIM™ instrument accounted for 26.3% of the variance in total PCA hours, Model Systems differences accounted for 9.3%, and no other predictor accounted for more than 2.1% of the variance.
Among them, the age of infant was a significant factor that accounted for 21.6% of PCA variance (Figure 4A), while other confounders such as host genetics, consumption of antibiotics, slight dietary differences during weaning and health status of the infants may account for small portions of the total PCA variance.
Total PCA morphine usages in the celecoxib group and controls were 17.6 ± 11.9 and 24.6 ± 14.6 mg, respectively (p = 0.03).
Waist hip ratio (WHR), a measure of central adiposity, was positively associated with PCa before age 65, and less strongly, with total PCa.
This study showed a weak association between tallness and risk of total PCa, also shown (but not significantly) by aggressive PCa or PCa in the <65 sub-cohort.
After adjustment for a number of possible confounders, the increased risk of total PCa associated with greater height was weakened (P for trend=0.08, Table 3).
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Not all patients have complete entries for each component in the database, so each component (pump, set, and drug) was analyzed separately, and the weighted average for total PCA-related costs was analyzed.
Life-time total and PCa-related costs were summarized by cancer stage.
Life-time total and PCa-related costs were discounted at a 3% annual rate.
Monthly treatment phase total and PCa-related costs that were input into the model are depicted in Table 1.
Cost estimates were then combined with survival data to yield total and PCa-related life-time costs.
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