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Example sentences for: totpar

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Criteria for inclusion for postoperative pain were: full journal publication, randomized controlled trials which included single dose treatment groups of oral rofecoxib and placebo, double blind design, baseline postoperative pain of moderate to severe intensity, patients over 15 years of age, at least 10 patients per group, and the pain outcome measures of total pain relief (TOTPAR) or summed pain intensity difference (SPID) over 4-6 hours or sufficient data to allow their calculation.
Some information was available for TOTPAR calculated to eight hours, but not in a dichotomous format.
All five trials gave or allowed the calculation of six-hour TOTPAR and the derivation of the number of patients with at least 50%maxTOTPAR.
For each trial, mean TOTPAR, SPID, VASTOTPAR or VASSPID values for each treatment group were converted to %maxTOTPAR by division into the calculated maximum value [ 15 ] . The proportion of patients in each treatment group who achieved at least 50%maxTOTPAR was calculated using valid equations [ 16 17 18 ] . The number of patients randomized was taken as the basis for calculations, to produce an intention to treat analysis.
Pain measures allowed for the calculation of TOTPAR or SPID were a standard five point pain relief scale (none, slight, moderate, good, complete), a standard four point pain intensity scale (none, mild, moderate, severe) or a standard visual analogue scale (VAS) for pain relief or pain intensity.