HIV-related bronchiectasis in children: an emerging spectre in high tuberculosis burden areas
BACKGROUND: Human immunodeficiency virus (HIV) infected children have an eleven-fold risk of acute lower respiratory tract infection. This places HIV-infected children at risk of airway destruction and bronchiectasis.OBJECTIVE: To study predisposing factors for the development of bronchiectasis in a...
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Veröffentlicht in: | The international journal of tuberculosis and lung disease 2012-01, Vol.16 (1), p.114-119 |
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Zusammenfassung: | BACKGROUND: Human immunodeficiency virus (HIV) infected children have an eleven-fold risk of acute lower respiratory tract infection. This places HIV-infected children at risk of airway destruction and bronchiectasis.OBJECTIVE: To study predisposing factors for the development of
bronchiectasis in a developing world setting.METHODS: Children with HIV-related bronchiectasis aged 6-14 years were enrolled. Data were collected on demographics, induced sputum for tuberculosis, respiratory viruses (respiratory syncytial virus), influenza A and B, parainfluenza
1-3, adenovirus and cytomegalovirus), bacteriology and cytokines. Spirometry was performed. Blood samples were obtained for HIV staging, immunoglobulins, immunoCAP®-specific immunoglobulin E (IgE) for common foods and aeroallergens and cytokines.RESULTS: In all, 35 patients were
enrolled in the study. Of 161 sputum samples, the predominant organisms cultured were Haemophilus influenzae and parainfluenzae (49%). The median forced expiratory volume in 1 second of all patients was 53%. Interleukin-8 was the predominant cytokine in sputum and serum. The
median IgE level was 770 kU/l; however, this did not seem to be related to atopy; 36% were exposed to environmental tobacco smoke, with no correlation between exposure and CD4 count.CONCLUSION: Children with HIV-related bronchiectasis are diagnosed after the age of 6 years and suffer significant
morbidity. Immune stimulation mechanisms in these children are intact despite the level of immunosuppression. |
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ISSN: | 1027-3719 1815-7920 |
DOI: | 10.5588/ijtld.11.0244 |