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1 ven approaches wherein a circuit of interest is defined a priori.
2 , 279 (37.5%) were in a high-risk group that was defined a priori.
3 ere were 21 reported secondary outcomes that were defined a priori.
4 e date for the paired controls; time windows were defined a priori.
5 motor, diplopia, and HRQOL criteria, success was defined a priori and applied separately and in combi
6  Cutoffs for deranged physiologic parameters were defined a priori and their association with in-hosp
7                       Successful weight loss was defined a priori as > or = 40% EWL in each of four 6
8                                     Response was defined a priori as a > or =50% reduction in the sco
9                            Clinical response was defined a priori as a decrease of 50% or more from b
10      The primary outcome, symptom remission, was defined a priori as a total exit score of </=7 on th
11                       Meeting the DMG bundle was defined a priori as achieving any 7 of the 9 end poi
12                 Donor management goals "met" was defined a priori as achieving any seven of the nine
13                         The primary endpoint was defined a priori as the first occurrence of cardiova
14                                         CCMs were defined a priori as interventions with at least thr
15 ale (HAM-A) and Visual Analog Scale for Pain were defined a priori as key secondary outcome measures.
16 samorelin, those with >/=8% reduction in VAT were defined a priori as responders per the statistical
17                        Response and euthymia were defined, a priori, as at least a 50% improvement fr
18                A "target value" of mortality was defined a priori for each stratum, to guide the inte
19 subgroups should be few in number and should be defined a priori on the basis of variables present be
20                          The primary outcome was defined a priori prior to data extraction.

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