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Session 26
Oral Abstract Presentations Metabolic and Opportunistic Infectious Complications of HIV Disease Session Day and Time: Thursday 10 am - 12:45 pm Presentation Time: 11:15 Room: Auditorium |
Background:
Immunization with 23-valent pneumococcal polysaccharide vaccine (PPV) may
increase incidence of pneumonia in HIV-1-infected patients (pts) not receiving
HAART in Africa.
Methods: Pts receiving and not receiving 23-valent PPV were
prospectively observed for changes of CD4+ and PVL at wk 4 of
vaccination and at the end of study and development of pneumococcal disease
(PD), all causes of community-acquired pneumonia (CAP) and new AIDS-defining
opportunistic illness (OI), and mortality at NTUH in Taiwan between June 1,
2000 and September 30, 2002. The Cox-proportional hazards model was used to
assess the impact of the pneumococcal vaccination with and without adjustment
for age,
sex, risk behavior for HIV transmission, baseline CD4+ count, PVL,
baseline OI, and use of HAART. Odds
ratios and 95% confidence intervals (95% CI) were also calculated for risk analyses.
All tests were two-tailed. A p
value < 0.05 was considered significant.
Results: A total of 305 HIV-1 infected pts received PPV and
98.2% received HAART whose median baseline CD4+ count and PVL were
0.179 x 109/L and 3,850 copies/ml, respectively. 203 patients, 84.2%
receiving HAART, did not receive PPV and their median baseline CD4+
count was 0.195 x 109/L and PVL 42,900 copies/ml. The incidence of
PD among vaccinees was 2.2 per 1,000 PY over the median observation of 641 days
while that for non-vaccinees was 22.9 per 1,000 pt years over the observation
of 500 days (p = 0.007). The adjusted odds ratio (AOR) for developing PD of
vaccinees as compared to non-vaccinees was 0.081 (95% CI, 0.009–0.724; p = 0.02). The median CD4+ count increased by 0.045 x 109/L
and PVL decreased by 130 copies/ml after one month of pneumococcal vaccination
among the selected 31 vaccinees. The AOR of developing all cause CAP and new OI
of vaccinees as compared to non-vaccinees was 1.393 (95% CI, 0.478–4.059, p =
0.54) and 1.074 (95% CI, 0.310–3.716, p = 0.91), respectively. AOR for death of
vaccinees as compared to non-vaccinees was 0.144 (95% CI, 0.041–0.505, p = 0.002).
Conclusions: Our data indicated that immunization with
23-valent PPV reduced risk for PD and death among HIV-1-infected pts who were
treated with HAART. Vaccination did not increase PVL or the risks for
developing all cause CAP and HIV progression.