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In evaluating trials of new drugs and procedures, the Food and Drug Administration does not accept such subgroup analyses, requiring a second trial for the subgroup that may benefit.
Average improvements are, and should be, relevant to organizations such as the N.H.S., but only individual or subgroup analyses can reveal the full range of effective therapies.
Subgroup analyses did not change the findings.
Thus, additional subgroup analyses are necessary.
Where possible, we also performed subgroup analyses for gender.
Therefore, subgroup analyses were performed as described in Table 4.
We then consider selected subgroup analyses and conclude.
This article quantifies the error rates associated with subgroup analyses.
Subgroup analyses were conducted to explore potential explanations for inconsistencies.
It is important to distinguish these overinterpreted, misused, and unplanned subgroup analyses from those prespecified and well-designed subgroup analyses.
All the subgroup analyses and sensitivity analyses are reported in Fig. 7.
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