Increased disease burden and antibiotic resistance of bacteria causing severe community-acquired lower respiratory tract infections in human immunodeficiency virus type 1-infected children
Abstract
To improve the management of lower respiratory tract infections (LRTI) in human immunodeficiency virus type 1 (HIV-1)-infected children, we assessed the burden of disease, clinical outcome and antibiotic susceptibility of bacteria causing severe community-acquired LRTI in children. A prospective, descriptive study was performed in the pediatric wards at a secondary and tertiary care hospital in South Africa. Urban black children aged 2-60 months admitted with severe acute LRTI from March 1997 through February 1998 were enrolled. HIV-1 infection was present in 45.1% of 1215 cases of severe LRTI. Bacteremia occurred in 14.9% of HIV-1-infected and in 6.5% of HIV-1-uninfected children (P<.00001). The estimated relative incidence of bacteremic severe LRTI in children aged from 2 to 24 months were greater in HIV-1-infected than in -uninfected children for Streptococcus pneumoniae (risk ratio [RR], 42.9; 95% confidence interval [CI], 20.7-90.2), Haemophilus influenzae type b (RR, 21.4; 95% CI, 9.4-48.4), Staphylococcus aureus (RR, 97.9; 95% CI, 11.4-838.2) and Escherichia coli (RR, 49.0; 95% CI, 15.4-156). Isolation of Mycobacterium tuberculosis was also more common in HIV-1-infected than in -uninfected children (RR, 22.5; 95% CI, 13.4-37.6). In HIV-1-infected children, 60% of S. aureus and 85.7% of E. coli isolates were resistant to methicillin and trimethoprim-sulfamethoxazole, respectively. The case-fatality rates among HIV-1-infected children was 13.1%, and among HIV-1-uninfected children, 2.1% (adjusted odds ratio [AOR]; 6.52, 95% CI, 3.53-12.05; P<.00001). The changing spectrum of bacteria and antibiotic susceptibility patterns in HIV-1-infected children requires a reevaluation of the empirical treatment of community-acquired severe LRTI in children from developing countries with a high prevalence of childhood HIV-1 infection.
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HIV-infected children have a greatly increased risk of pneumonia, particularly bacterial pneumonia caused by S pneumoniae and H influenzae.
“Children infected with HIV have a greatly increased risk of pneumonia, particularly bacterial pneumonia (S pneumoniae and H influenzae).61”
From Global burden of childhood pneumonia and diarrhoea (2013) · cites this paper as [61]
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- Authors
- Madhi, S. A., Petersen, K., Madhi, A., Khoosal, M., & Klugman, K. P.
- Affiliations
- University of the Witwatersrand (ZA)
- South African Institute for Medical Research (ZA)
- Corresponding author
- Madhi, S. A.
- Venue
- Clinical Infectious Diseases
- Publisher
- Oxford University Press (OUP)
- Published
- 2000-07-01
- Volume
- 31
- Issue
- 1
- Pages
- 170-176
- ISSN
- 1058-4838 (ISSN-L)
- 1537-6591
- OpenAlex
- W2098698934
- Cited by
- 254
- References
- 24
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 1 · 2023: 5 · 2022: 7 · 2021: 7 · 2020: 4 · 2019: 9 · 2018: 5 · 2017: 7 · 2016: 14 · 2015: 16 · 2014: 12 · 2013: 12 · 2012: 12
- FWCI
- 6.68
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Clinical Infectious Diseases (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Pneumonia and Respiratory Infections
- Health Sciences › Medicine › Infectious Diseases › HIV/AIDS Research and Interventions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Antibiotic Resistance in Bacteria
- Keywords
- HIV-1 infection, pediatric lower respiratory tract infection, community-acquired pneumonia, bacteremia, Streptococcus pneumoniae, Haemophilus influenzae type b, Staphylococcus aureus, Escherichia coli, Mycobacterium tuberculosis, antibiotic resistance, methicillin resistance, trimethoprim-sulfamethoxazole resistance, case fatality, disease burden
- MeSH terms
- Child, Preschool, Drug Resistance, Microbial, Haemophilus Infections, Haemophilus influenzae, Humans, Infant, Mycobacterium tuberculosis, Pneumonia, Pneumococcal, Prospective Studies, Staphylococcal Infections, Tuberculosis, Pulmonary, HIV-1, Bacteremia, AIDS-Related Opportunistic Infections, Community-Acquired Infections, Pneumonia, Bacterial
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