Bacterial community acquired pneumonia in HIV-infected inpatients in the highly active antiretroviral therapy era

被引:41
|
作者
Madeddu, G. [1 ,2 ]
Porqueddu, E. M. [2 ]
Cambosu, F. [2 ]
Saba, F. [2 ]
Fois, A. G. [3 ]
Pirina, P. [3 ]
Mura, M. S. [2 ]
机构
[1] Univ Sassari, Osped Civile Nuovo, Inst Malattie Infett, I-07100 Sassari, Italy
[2] Univ Sassari, Dept Infect Dis, I-07100 Sassari, Italy
[3] Univ Sassari, Dept Resp Dis, I-07100 Sassari, Italy
关键词
D O I
10.1007/s15010-007-7162-0
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: Highly active antiretroviral therapy (HAART) has deeply modified HIV/AIDS related morbidity and mortality. However, bacterial community acquired pneumonia (BCAP) still represents one of the most frequent causes of morbidity in HIV-infected patients with an inpatient 10% mortality rate. Objectives: We retrospectively studied the characteristics of BCAP in consecutive HIV-infected inpatients hospitalized from 1999 to 2004 and evaluated the presence of risk factors and the influence of combination antiretroviral therapy receipt on BCAP outcomes. Results: We studied 84 BCAP episodes in 76 HIV-infected inpatients (63 males and 13 females) aged 27-80 years. Thirty-two (42.1%) patients were receiving combination antiretroviral treatment (CART) while 44 (57.9%) were not treated (NART). BCAP incidence progressively increased from 1999 to 2004. The overall percentage of injection drug users was > 84%, of smokers > 88% and alcohol abusers > 32% with no statistical difference between CART and NART. Streptococcus pneumoniae was the most frequently identified pathogen (60%). Time to clinical stability was significantly Longer in NART in respect of CART (p = 0.011). In multivariate analysis, CDC stage C, CD4 cell count < 100 X 10(6) cells/l, and S. pneumoniae etiology were predictors for time to clinical stability > 7 days, while receipt of antiretroviral therapy was protective. The percentage of deaths did not differ between CART and NART; most patients had a CD4 count < 200 x 10(6) cells/l or severe concomitant diseases. Conclusions: The incidence of BCAP was high in HIV-infected inpatients observed in the present study mainly due to HIV infection itself, IVDU, alcohol abuse and smoking habit. A longer time to clinical stability was associated with advanced HIV infection and with S. pneumoniae etiology, while receipt of antiretroviral therapy was protective. Injection drug abuse treatment, alcohol abuse and smoking cessation programs, antiretroviral treatment adherence support and pneumococcal vaccination should be implemented to reduce the incidence and to improve the outcomes of BCAP in HIV-infected patients.
引用
收藏
页码:231 / 236
页数:6
相关论文
共 50 条
  • [1] Bacterial Community Acquired Pneumonia in HIV-Infected Inpatients in the Highly Active Antiretroviral Therapy Era
    G. Madeddu
    E. M. Porqueddu
    F. Cambosu
    F. Saba
    A. G. Fois
    P. Pirina
    M. S. Mura
    Infection, 2008, 36 : 231 - 236
  • [2] Bacterial community acquired pneumonia in HIV infected inpatients in the highly active Antiretroviral therapy era
    Madeddu, G.
    Porqueddu, M. E.
    Saba, F.
    Fois, A. G.
    Pirina, P.
    Mura, M. S.
    EACS: Proceedings of the 10th European Aids Conference, 2005, : 39 - 42
  • [3] Incidence of pneumonia in HIV-infected patients in the highly active antiretroviral therapy era
    Velasco Arribas, Maria
    Satue Bartolome, Jose Angel
    Losa Garcia, Juan Emilio
    Espinosa Gimeno, Alfredo
    Delgado-Iribarren, Alberto
    Castilla Castellano, Virgilio
    MEDICINA CLINICA, 2007, 128 (04): : 130 - 132
  • [4] Effect of highly active antiretroviral therapy on the incidence of bacterial pneumonia in HIV-infected subjects
    Donati, KD
    Bertagnolio, S
    Tumbarello, M
    Tacconelli, E
    Cataldo, M
    Longo, B
    Cauda, R
    INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2000, 16 (03) : 357 - 360
  • [5] HIV-associated community-acquired pneumonia in the highly active antiretroviral therapy era
    Viale, P
    Scudeller, L
    Signorini, L
    Cadeo, B
    Petrosillo, N
    Pagani, L
    Carosi, G
    AIDS, 2002, 16 (17) : 2361 - 2362
  • [6] Pruritus in HIV-infected patients in the era of highly active antiretroviral therapy
    Blanes, Mar
    Belinchon, Isabel
    Betlloch, Isabel
    Portilla, Joaquin
    Reus, Sergio
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2009, 60 (03) : AB119 - AB119
  • [7] Sarcoidosis in HIV-infected patients in the era of highly active antiretroviral therapy
    Foulon, G
    Wislez, M
    Naccache, JM
    Blanc, FX
    Rabbat, A
    Israël-Biet, D
    Valeyre, D
    Mayaud, C
    Cadranel, J
    CLINICAL INFECTIOUS DISEASES, 2004, 38 (03) : 418 - 425
  • [8] Hospitalized HIV-Infected Patients in the Era of Highly Active Antiretroviral Therapy
    Metsch, Lisa R.
    Bell, Christine
    Pereyra, Margaret
    Cardenas, Gabriel
    Sullivan, Tanisha
    Rodriguez, Allan
    Gooden, Lauren
    Khoury, Nayla
    Kuper, Tamy
    Brewer, Toye
    del Rio, Carlos
    AMERICAN JOURNAL OF PUBLIC HEALTH, 2009, 99 (06) : 1045 - 1049
  • [9] HIV-associated bacterial pneumonia in the era of highly active antiretroviral therapy
    Tumbarello, M
    Tacconelli, E
    Donati, KD
    Cauda, R
    JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY, 1999, 20 (02): : 208 - 209
  • [10] Treatment of tuberculosis in HIV-infected persons in the era of highly active antiretroviral therapy
    Dean, GL
    Edwards, SG
    Ives, NJ
    Matthews, G
    Fox, EF
    Navaratne, L
    Fisher, M
    Taylor, GP
    Miller, R
    Taylor, CB
    de Ruiter, A
    Pozniak, AL
    AIDS, 2002, 16 (01) : 75 - 83