TY - JOUR
T1 - Pertussis-associated pneumonia in infants and children from low-and middle-income countries participating in the perch study
AU - Barger-Kamate, Breanna
AU - Knoll, Maria Deloria
AU - Kagucia, E. Wangeci
AU - Prosperi, Christine
AU - Baggett, Henry C.
AU - Brooks, W. Abdullah
AU - Feikin, Daniel R.
AU - Hammitt, Laura L.
AU - Howie, Stephen R.C.
AU - Levine, Orin S.
AU - Madhi, Shabir A.
AU - Scott, J. Anthony G.
AU - Thea, Donald M.
AU - Amornintapichet, Tussanee
AU - Anderson, Trevor P.
AU - Awori, Juliet O.
AU - Baillie, Vicky L.
AU - Chipeta, James
AU - DeLuca, Andrea N.
AU - Driscoll, Amanda J.
AU - Goswami, Doli
AU - Higdon, Melissa M.
AU - Hossain, Lokman
AU - Karron, Ruth A.
AU - Maloney, Susan
AU - Moore, David P.
AU - Morpeth, Susan C.
AU - Mwananyanda, Lawrence
AU - Ofordile, Ogochukwu
AU - Olutunde, Emmanuel
AU - Park, Daniel E.
AU - Sow, Samba O.
AU - Tapia, Milagritos D.
AU - Murdoch, David R.
AU - O'Brien, Katherine L.
AU - Kotloff, Karen L.
N1 - Funding Information:
Financial support. This work was supported by a grant from the Bill and Melinda Gates Foundation (grant number 48968) to the International Vaccine Access Center, Department of International Health, Johns Hopkins Bloomberg School of Public Health. Travel for B. B.-K. was supported by the Fogarty International Clinical Research Scholars and Fellows Program at Vanderbilt University (grant number R24 TW007988).
Publisher Copyright:
© The Author 2016.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - Background. Few data exist describing pertussis epidemiology among infants and children in low-and middle-income countries to guide preventive strategies. Methods. Children 1-59 months of age hospitalized withWorld Health Organization-defined severe or very severe pneumonia in 7 African and Asian countries and similarly aged community controls were enrolled in the Pneumonia Etiology Research for Child Health study. They underwent a standardized clinical evaluation and provided nasopharyngeal and oropharyngeal swabs and induced sputum (cases only) for Bordetella pertussis polymerase chain reaction. Risk factors and pertussis-associated clinical findings were identified. Results. Bordetella pertussis was detected in 53 of 4200 (1.3%) cases and 11 of 5196 (0.2%) controls. In the age stratum1-5months, 40 (2.3% of 1721) cases were positive, all from African sites, as were 8 (0.5% of 1617) controls. Pertussis-positive African cases 1-5 months old, compared to controls, were more often human immunodeficiency virus (HIV) uninfected-exposed (adjusted odds ratio [aOR], 2.2), unvaccinated (aOR, 3.7), underweight (aOR, 6.3), and too young to be immunized (aOR, 16.1) (all P ? .05). Compared with pertussisnegative African cases in this age group, pertussis-positive cases were younger, more likely to vomit (aOR, 2.6), to cough ?14 days (aOR, 6.3), to have leukocyte counts >20 000 cells/?L (aOR, 4.6), and to have lymphocyte counts >10 000 cells/?L (aOR, 7.2) (all P ? .05). The case fatality ratio of pertussis-infected pneumonia cases 1-5 months of age was 12.5% (95% confidence interval, 4.2%-26.8%; 5/40); pertussis was identified in 3.7% of 137 in-hospital deaths among African cases in this age group. Conclusions. In the postneonatal period, pertussis causes a small fraction of hospitalized pneumonia cases and deaths; however, case fatality is substantial. The propensity to infect unvaccinated infants and those at risk for insufficient immunity (too young to be vaccinated, premature, HIV-infected/exposed) suggests that the role for maternal vaccination should be considered along with efforts to reduce exposure to risk factors and to optimize childhood pertussis vaccination coverage.
AB - Background. Few data exist describing pertussis epidemiology among infants and children in low-and middle-income countries to guide preventive strategies. Methods. Children 1-59 months of age hospitalized withWorld Health Organization-defined severe or very severe pneumonia in 7 African and Asian countries and similarly aged community controls were enrolled in the Pneumonia Etiology Research for Child Health study. They underwent a standardized clinical evaluation and provided nasopharyngeal and oropharyngeal swabs and induced sputum (cases only) for Bordetella pertussis polymerase chain reaction. Risk factors and pertussis-associated clinical findings were identified. Results. Bordetella pertussis was detected in 53 of 4200 (1.3%) cases and 11 of 5196 (0.2%) controls. In the age stratum1-5months, 40 (2.3% of 1721) cases were positive, all from African sites, as were 8 (0.5% of 1617) controls. Pertussis-positive African cases 1-5 months old, compared to controls, were more often human immunodeficiency virus (HIV) uninfected-exposed (adjusted odds ratio [aOR], 2.2), unvaccinated (aOR, 3.7), underweight (aOR, 6.3), and too young to be immunized (aOR, 16.1) (all P ? .05). Compared with pertussisnegative African cases in this age group, pertussis-positive cases were younger, more likely to vomit (aOR, 2.6), to cough ?14 days (aOR, 6.3), to have leukocyte counts >20 000 cells/?L (aOR, 4.6), and to have lymphocyte counts >10 000 cells/?L (aOR, 7.2) (all P ? .05). The case fatality ratio of pertussis-infected pneumonia cases 1-5 months of age was 12.5% (95% confidence interval, 4.2%-26.8%; 5/40); pertussis was identified in 3.7% of 137 in-hospital deaths among African cases in this age group. Conclusions. In the postneonatal period, pertussis causes a small fraction of hospitalized pneumonia cases and deaths; however, case fatality is substantial. The propensity to infect unvaccinated infants and those at risk for insufficient immunity (too young to be vaccinated, premature, HIV-infected/exposed) suggests that the role for maternal vaccination should be considered along with efforts to reduce exposure to risk factors and to optimize childhood pertussis vaccination coverage.
KW - Infant
KW - Pertussis
KW - Pneumonia
KW - Vaccination
KW - Whooping cough
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U2 - 10.1093/cid/ciw546
DO - 10.1093/cid/ciw546
M3 - Article
C2 - 27838672
AN - SCOPUS:85015933929
SN - 1058-4838
VL - 63
SP - S187-S196
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
ER -