Giuseppe
Emeritus
[Source: JAMA, <cite cite="http://jama.ama-assn.org/cgi/content/abstract/303/20/2051?etoc">JAMA -- Abstract: Viral Etiology of Severe Pneumonia Among Kenyan Infants and Children, May 26, 2010, Berkley et al. 303 (20): 2051</cite>. Abstract, edited.]
Vol. 303 No. 20, May 26, 2010
Viral Etiology of Severe Pneumonia Among Kenyan Infants and Children
James A. Berkley, FRCPCH; Patrick Munywoki, MSc; Mwanajuma Ngama, HND; Sidi Kazungu, RN; John Abwao, HND; Anne Bett, HND; Ria Lassauni?re, BSc; Tina Kresfelder, PhD; Patricia A. Cane, PhD; Marietjie Venter, PhD; J. Anthony G. Scott, FRCP; D. James Nokes, PhD
JAMA. 2010;303(20):2051-2057.
Context
Pneumonia is the leading cause of childhood death in sub-Saharan Africa. Comparative estimates of the contribution of causative pathogens to the burden of disease are essential for targeted vaccine development.
Objective
To determine the viral etiology of severe pneumonia among infants and children at a rural Kenyan hospital using comprehensive and sensitive molecular diagnostic techniques.
Design, Setting, and Participants
Prospective observational and case-control study during 2007 in a rural Kenyan district hospital. Participants were children aged 1 day to 12 years, residing in a systematically enumerated catchment area, and who either were admitted to Kilifi District Hospital meeting World Health Organization clinical criteria for severe pneumonia or very severe pneumonia; (2) presented with mild upper respiratory tract infection but were not admitted; or (3) were well infants and children attending for immunization.
Main Outcome Measures
The presence of respiratory viruses and the odds ratio for admission with severe disease.
Results
Of 922 eligible admitted patients, 759 were sampled (82% [median age, 9 months]). One or more respiratory viruses were detected in 425 of the 759 sampled (56% [95% confidence interval {CI}, 52%-60%]). Respiratory syncytial virus (RSV) was detected in 260 participants (34% [95% CI, 31%-38%]) and other respiratory viruses were detected in 219 participants (29%; 95% CI, 26%-32%), the most common being Human coronavirus 229E (n = 51 [6.7%]), influenza type A (n = 44 [5.8%]), Parainfluenza type 3 (n = 29 [3.8%]), Human adenovirus (n = 29 [3.8%]), and Human metapneumovirus (n = 23 [3.0%]). Compared with well control participants, detection of RSV was associated with severe disease (5% in control participants; adjusted odds ratio, 6.11 [95% CI, 1.65-22.6]) while collectively, other respiratory viruses were not associated with severe disease (23% in control participants; adjusted odds ratio, 1.27 [95% CI, 0.64-2.52]).
Conclusion
In a sample of Kenyan infants and children admitted with severe pneumonia to a rural hospital, RSV was the predominant viral pathogen.
Author Affiliations:
Kenya Medical Research Institute (KEMRI), Centre for Geographic Medicine Research?Coast, Kilifi, Kenya (Drs Berkley, Scott, and Nokes, Messrs Munywoki and Abwao, and Mss Ngama, Kazungu, and Bett); Centre for Clinical Vaccinology & Tropical Medicine, University of Oxford, Oxford, England (Drs Berkley and Scott); Respiratory and Zoonotic Virus Programme, Department of Medical Virology, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa (Ms Lassauni?re and Drs Kresfelder and Venter); Centre for Infections, Health Protection Agency, Colindale, London, England (Dr Cane); Respiratory Virus Unit, National Institute for Communicable Diseases, Sandringham, South Africa (Dr Venter); and Department of Biological Sciences, University of Warwick, Coventry, England (Dr Nokes).
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Vol. 303 No. 20, May 26, 2010
Viral Etiology of Severe Pneumonia Among Kenyan Infants and Children
James A. Berkley, FRCPCH; Patrick Munywoki, MSc; Mwanajuma Ngama, HND; Sidi Kazungu, RN; John Abwao, HND; Anne Bett, HND; Ria Lassauni?re, BSc; Tina Kresfelder, PhD; Patricia A. Cane, PhD; Marietjie Venter, PhD; J. Anthony G. Scott, FRCP; D. James Nokes, PhD
JAMA. 2010;303(20):2051-2057.
Context
Pneumonia is the leading cause of childhood death in sub-Saharan Africa. Comparative estimates of the contribution of causative pathogens to the burden of disease are essential for targeted vaccine development.
Objective
To determine the viral etiology of severe pneumonia among infants and children at a rural Kenyan hospital using comprehensive and sensitive molecular diagnostic techniques.
Design, Setting, and Participants
Prospective observational and case-control study during 2007 in a rural Kenyan district hospital. Participants were children aged 1 day to 12 years, residing in a systematically enumerated catchment area, and who either were admitted to Kilifi District Hospital meeting World Health Organization clinical criteria for severe pneumonia or very severe pneumonia; (2) presented with mild upper respiratory tract infection but were not admitted; or (3) were well infants and children attending for immunization.
Main Outcome Measures
The presence of respiratory viruses and the odds ratio for admission with severe disease.
Results
Of 922 eligible admitted patients, 759 were sampled (82% [median age, 9 months]). One or more respiratory viruses were detected in 425 of the 759 sampled (56% [95% confidence interval {CI}, 52%-60%]). Respiratory syncytial virus (RSV) was detected in 260 participants (34% [95% CI, 31%-38%]) and other respiratory viruses were detected in 219 participants (29%; 95% CI, 26%-32%), the most common being Human coronavirus 229E (n = 51 [6.7%]), influenza type A (n = 44 [5.8%]), Parainfluenza type 3 (n = 29 [3.8%]), Human adenovirus (n = 29 [3.8%]), and Human metapneumovirus (n = 23 [3.0%]). Compared with well control participants, detection of RSV was associated with severe disease (5% in control participants; adjusted odds ratio, 6.11 [95% CI, 1.65-22.6]) while collectively, other respiratory viruses were not associated with severe disease (23% in control participants; adjusted odds ratio, 1.27 [95% CI, 0.64-2.52]).
Conclusion
In a sample of Kenyan infants and children admitted with severe pneumonia to a rural hospital, RSV was the predominant viral pathogen.
Author Affiliations:
Kenya Medical Research Institute (KEMRI), Centre for Geographic Medicine Research?Coast, Kilifi, Kenya (Drs Berkley, Scott, and Nokes, Messrs Munywoki and Abwao, and Mss Ngama, Kazungu, and Bett); Centre for Clinical Vaccinology & Tropical Medicine, University of Oxford, Oxford, England (Drs Berkley and Scott); Respiratory and Zoonotic Virus Programme, Department of Medical Virology, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa (Ms Lassauni?re and Drs Kresfelder and Venter); Centre for Infections, Health Protection Agency, Colindale, London, England (Dr Cane); Respiratory Virus Unit, National Institute for Communicable Diseases, Sandringham, South Africa (Dr Venter); and Department of Biological Sciences, University of Warwick, Coventry, England (Dr Nokes).
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