Invasive Pneumococcal Disease in HIV-Infected Adults: Clinical Changes After the Introduction of the Pneumococcal Conjugate Vaccine in Children

被引:11
|
作者
Burgos, Joaquin [1 ]
Penaranda, Maria [2 ]
Payeras, Antoni [3 ]
Villoslada, Aroa [3 ]
Curran, Adrian [1 ]
Garau, Margarita [4 ]
Riera, Melcior [2 ]
Crespo, Manuel [1 ]
Navarro, Jordi [1 ]
Van den Eynde, Eva [1 ]
Maria Planes, Ana [5 ]
Ribera, Esteban [1 ]
Pahissa, Albert [1 ]
Falco, Vicenc [1 ]
机构
[1] Univ Autonoma Barcelona, Dept Infect Dis, Hosp Univ Vall Hebron, Barcelona 08035, Spain
[2] Hosp Son Dureta, Dept Internal Med, Palma de Mallorca, Spain
[3] Hosp Son Llatzer, Dept Internal Med, Palma de Mallorca, Spain
[4] Hosp Son Llatzer, Dept Microbiol, Palma de Mallorca, Spain
[5] Univ Autonoma Barcelona, Dept Microbiol, Hosp Univ Vall Hebron, Barcelona 08035, Spain
关键词
HIV-infected patients; invasive pneumococcal disease; pneumococcal conjugated vaccine; Streptococcus pneumonia; HUMAN-IMMUNODEFICIENCY-VIRUS; STREPTOCOCCUS-PNEUMONIAE; ERA; IMPACT; EPIDEMIOLOGY; EMERGENCE; SEROTYPES; BARCELONA; TRENDS; AIDS;
D O I
10.1097/QAI.0b013e31823d0f5f
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Few data exist on the implications of widespread use of 7-valent pneumococcal conjugate vaccine in children in the invasive pneumococcal disease (IPD) in HIV-infected adults. We conducted a multicenter study to analyze differences in clinical presentation of IPD between HIV-infected and non-HIV-infected adults in the prevaccine and postvaccine era. Methods: Study of all cases of IPD in HIV-infected adults diagnosed since 1996 to 2010. Episodes were classified into prevaccine (1996-2001), early postvaccine (2002-2004), and late postvaccine period (2005-2010). For each case, we identified an HIV-negative control patient with IPD matched by hospital, age, and vaccine period. Results: Two hundred twenty-one episodes of IPD in HIV-infected patients were diagnosed. The incidence of IPD decreased from 7.81 to 3.69 episodes per 1000 patient-years (-53%; 95% confidence interval: -65% to -36%, P < 0.001) between prevaccine and late postvaccine period. There was an 81% (95% confidence interval: -88% to -69%, P < 0.001) decrease of IPD caused by vaccine serotypes. In late postvaccine period IPD in HIV-infected patients was associated to higher rates of respiratory failure (28.4% vs. 48.4%, P = 0.011), greater intensive care unit admission (8.2% vs. 21.7%, P = 0.02) and a higher need for mechanical ventilation (5.9% vs. 16.3%, P = 0.033). In the prevaccine period, non-HIV-infected patients had a more severe illness than in those with HIV infection; however, these differences disappeared in the late postvaccine period. Conclusions: In the late postvaccine era, the incidence of IPD in HIV-infected patients has decreased, however, clinical presentation seems to have changed to a more severe illness. The widespread use of highly active antiretroviral therapy, polyssacharide vaccine, and 7-valent pneumococcal conjugate vaccine has contributed to these changes.
引用
收藏
页码:31 / 38
页数:8
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