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To the Editor—We appreciate the comments by Sogaard et al. [1]. They suggest that we may have overestimated the efficacy of the 23-valent pneumococcal polysaccharide vaccine (PPV) among HIV-infected patients, because current guidelines do not actively recommend that PPV be administered to persons with CD4+ cell counts <200 cells/µL (who are more likely to have an episode of pneumonia) and because we did not use time-varying CD4+ cell count measurements in our models. These are interesting points to which we are pleased to respond.

If persons with lower CD4+ cell counts were less likely to have received PPV, our analyses would have been biased. However, CD4+ cell count at baseline was not associated with a history of PPV vaccination (67% of patients with CD4+ cell count <200 cells/µL were vaccinated, and 69% of patients with CD4+ cell counts ⩾200 cells/µL were vaccinated; P = .67). Specifically, current guidelines recommend that all patients with a CD4+ cell count ⩾200 cells/µL receive PPV and that PPV vaccination be considered for those with a CD4+ cell count <200 cells/µL [2]. Other guidelines recommend vaccination of all HIV-infected patients when a diagnosis of HIV infection is determined [3]. An informal survey conducted several years ago among HIV clinicians at Veterans Affairs hospitals revealed that there was not a consistent policy among the different Veterans Affairs HIV clinics or among different practitioners within a clinic regarding these recommendations (M.C.R.-B., unpublished observations). Thus, we have no evidence that patients with higher CD4+ cell counts were more likely to receive PPV. Nevertheless, baseline CD4+ cell count was related to risk of pneumonia; 46% of patients with a CD4+ cell count <200 cells/µL experienced a pneumonia event, and only 7% of patients with a CD4+ cell count ⩾200 cells/µL experienced such an event (P < .001). This is consistent with data from many other observational studies [4].

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