Figure 1
Figure 1. Impact of donor CMV status on antiviral use. (A) The number of days that each D+/R+ or D−/R+ recipient received antiviral drug therapy (GCV or foscarnet). The box plot overlays show the median and the central 50% of the data. The median is zero for the D+/R+ group, as the majority did not require antivirals. P value determined by rank-sum test. (B) The cumulative incidence of antiviral use, estimated by the method of Kalbfleisch and Prentice,40 incorporates recurrent events. Most events occur between 30 to 90 days posttransplant, but the separation of the curves continues to increase, as late events occur more frequently in the D− group. The excess risk in the D− group was statistically significant, adjusted for pre-HCT covariates (P < .001) and for GVHD (P = .009, Table 3). DPT, days posttransplant.

Impact of donor CMV status on antiviral use. (A) The number of days that each D+/R+ or D/R+ recipient received antiviral drug therapy (GCV or foscarnet). The box plot overlays show the median and the central 50% of the data. The median is zero for the D+/R+ group, as the majority did not require antivirals. P value determined by rank-sum test. (B) The cumulative incidence of antiviral use, estimated by the method of Kalbfleisch and Prentice,40  incorporates recurrent events. Most events occur between 30 to 90 days posttransplant, but the separation of the curves continues to increase, as late events occur more frequently in the D group. The excess risk in the D group was statistically significant, adjusted for pre-HCT covariates (P < .001) and for GVHD (P = .009, Table 3). DPT, days posttransplant.

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