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In a multivariate regression model, factors favoring CD4+ T cell recovery ≥ 200 cells/µL were lower dose antithymocyte globulin (ATG) (hazard ratio [HR], 3.93; 95% confidence interval [CI], 2.3 to 5.83; P = .001), negative recipient cytomegalovirus (CMV) serostatus (HR, 3.76; 95% CI, 1.9 to 5.74; P = .001), and younger age (HR, 2.61; 95% CI, 1.01 to 3.47; P = .03).03
Prophylactic antiviral treatment for CMV was required in cases of a CMV positive donor graft and a CMV negative recipient.
After allotransplantation, cytomegalovirus (CMV) may be transmitted from the donor organ, giving rise to primary infection in a CMV negative recipient or reinfection in one who is CMV positive.
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Hospitals should avoid the need for elective transfusion of group O RhD negative red cells to non-O RhD negative recipients.
By contrast within the 28 transplants in HCV negative recipients, there were 26 patients with one transplant and one patient with two transplants.
Multivariate meta-regression showed no significant difference in CMV [cytomegalovirus] disease after allowing for potential confounding or effect-modification by prophylactic drug used, organ transplanted or recipient serostatus in CMV positive recipients and CMV negative recipients of CMV positive donors".
HCMV pneumonitis might be the consequence of a HCMV infection by a contaminated graft implanted in a HCMV-negative recipient.
The renal colonization of this strain was more than five times higher than that of the ShlA-negative recipient strain in an experimental rat pyelonephritis model.
Because all isolates in this report carried multiple plasmids, it was necessary to transfer the NDM-encoding plasmid to a plasmid-negative recipient for analysis.
Such organs would not be used for HIV-negative recipients because of the risk of infection.
The poor outcome of HCV-positive recipients has resulted in divergence in the transplant outcomes between HCV-positive recipients and HCV-negative recipients.
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