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Radiographically confirmed pneumonia in Malawian children and associated pneumococcal carriage after introduction of the 13-valent pneumococcal conjugate vaccine.
Mzumara, Grace; Chirombo, James; Swarthout, Todd D; Bar-Zeev, Naor; Harawa, Philliness Prisca; Jalloh, Mohamed Sanusi; Kirolos, Amir; Mukhula, Victoria; Newberry, Laura; Ogunlade, Olawale; Wachepa, Richard; French, Neil; Heyderman, Robert S; Iroh Tam, Pui-Ying.
  • Mzumara G; Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.
  • Chirombo J; University of Bergen, Bergen, Norway.
  • Swarthout TD; Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.
  • Bar-Zeev N; Department of Infection, Division of Infection and Immunity, University College London, London, UK.
  • Harawa PP; Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, Netherlands.
  • Jalloh MS; Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.
  • Kirolos A; University of Liverpool, Liverpool, UK.
  • Mukhula V; World Health Organization, Geneva, Switzerland.
  • Newberry L; Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.
  • Ogunlade O; Kamuzu University of Health Sciences, Blantyre, Malawi.
  • Wachepa R; Liverpool School of Tropical Medicine, Liverpool, UK.
  • French N; University of Liverpool, Liverpool, UK.
  • Heyderman RS; Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.
  • Iroh Tam PY; Malawi-Liverpool Wellcome Programme, Blantyre, Malawi.
Pneumonia (Nathan) ; 16(1): 23, 2024 Oct 05.
Article en En | MEDLINE | ID: mdl-39367515
ABSTRACT

BACKGROUND:

The 13-valent pneumococcal conjugate vaccine (PCV-13) was introduced in Malawi in 2011 with an expected impact of reducing pneumococcal pneumonia in children. We aimed to describe clinical characteristics and nasopharyngeal (NP) carriage of pneumococcus by serotype in children hospitalized with primary end-point pneumonia (PEP) between 2013 and 19 after the introduction of PCV-13.

METHODS:

We conducted a secondary analysis of children aged under-5-years hospitalized with acute respiratory illness (ARI) in Malawi. Chest radiographs conducted at admission were read by two independent clinicians according to WHO criteria for PEP, and a third reviewer resolved discordant diagnoses. NP swab specimens were processed and Streptococcus pneumoniae growth was serotyped. Multivariable regression analysis was conducted to assess the association between clinical characteristics, NP serotypes, and PEP.

RESULTS:

We had complete radiographic and NP serotype data for 500 children, of which 54 isolates were vaccine-type (VT) (10.8%), 165 were non-VT (NVT; 33.0%), and 281 had no pneumococcal growth (56.2%). Among these, 176 (35.2%) had PEP on chest x-ray. Among those with PEP, pneumococcal carriage was documented in 43.8% of cases, and VT serotypes accounted for 10.8%. For children with PEP, we found no association between clinical characteristics and carrying either VT, NVT, or no pneumococcus.

CONCLUSION:

Carriage of S. pneumoniae remains high among children hospitalized with ARI in Malawi, but children with VT carriage were no more likely to have PEP than children carrying no pneumococcus or those with NVT carriage. There were no differences in clinical characteristics between those carrying VT, NVT, or no pneumococcus.
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