Impact of the introduction of pneumococcal conjugate vaccination on invasive pneumococcal disease and pneumonia in The Gambia: 10 years of population-based surveillance - 25/08/21
The Gambia Pneumococcal Surveillance Group
Grant A Mackenzie, PhD a, b, c, d, ⁎
, Philip C Hill, ProfMD e, David J Jeffries, PhD a, Malick Ndiaye, DP a, Shah M Sahito, MSc a, Ilias Hossain, MPH a, Uchendu Uchendu, MD a, David Ameh, MPH a, Oyedeji Adeyemi, MBBS a, Jayani Pathirana, PhD a, Yekini Olatunji, MSc a, Baderinwa Abatan, FWACP a, Bilquees S Muhammad, MBBS a, Ebirim Ahameefula, MBBS a, Augustin E Fombah, FRACGP a, Banjo Adeshola, MBBS a, Babila G Lobga, MBBS a, Debasish Saha, PhD a, Roslyn Mackenzie, FRACGP a, Aderonke Odutola, FWACP a, Ian D Plumb, MBBS a, Aliu Akano, FMCR f, Bernard E Ebruke, FMCPaed a, Readon C Ideh, FWACP a, Bankole Kuti, FWACP a, Peter Githua, MSc a, Emmanuel Olutunde, FWACP a, Ogochukwu Ofordile, MBBS a, Edward Green, FRCP a, Effua Usuf, PhD a, Henry Badji, MSc a, Usman NA Ikumapayi, PhD a, Ahmed Manjang, MSc a, Rasheed Salaudeen, MSc a, E David Nsekpong, BSc a, Sheikh Jarju, DVM a, Martin Antonio, ProfPhD a, c, g, Sana Sambou, MSc h, Lamin Ceesay, MSc h, Yamundow Lowe-Jallow, MSc h, Sidat Fofana, MSc h, Momodou Jasseh, PhD a, Kim Mulholland, ProfMD b, c, Maria Knoll, PhD i, Orin S Levine, PhD i, Stephen R Howie, PhD a, e, j, Richard A Adegbola, ProfPhD k, Brian M Greenwood, ProfMD c, Tumani Corrah, Prof aSummary |
Background |
The Gambia introduced seven-valent pneumococcal conjugate vaccine (PCV7) in August 2009, followed by PCV13 in May, 2011, using a schedule of three primary doses without a booster dose or catch-up immunisation. We aimed to assess the long-term impact of PCV on disease incidence.
Methods |
We did 10 years of population-based surveillance for invasive pneumococcal disease (IPD) and WHO defined radiological pneumonia with consolidation in rural Gambia. The surveillance population included all Basse Health and Demographic Surveillance System residents aged 2 months or older. Nurses screened all outpatients and inpatients at all health facilities using standardised criteria for referral. Clinicians then applied criteria for patient investigation. We defined IPD as a compatible illness with isolation of Streptococcus pneumoniae from a normally sterile site (cerebrospinal fluid, blood, or pleural fluid). We compared disease incidence between baseline (May 12, 2008–May 11, 2010) and post-vaccine years (2016–2017), in children aged 2 months to 14 years, adjusting for changes in case ascertainment over time.
Findings |
We identified 22 728 patients for investigation and detected 342 cases of IPD and 2623 cases of radiological pneumonia. Among children aged 2–59 months, IPD incidence declined from 184 cases per 100 000 person-years to 38 cases per 100 000 person-years, an 80% reduction (95% CI 69–87). Non-pneumococcal bacteraemia incidence did not change significantly over time (incidence rate ratio 0·88; 95% CI, 0·64–1·21). We detected zero cases of vaccine-type IPD in the 2–11 month age group in 2016–17. Incidence of radiological pneumonia decreased by 33% (95% CI 24–40), from 10·5 to 7·0 per 1000 person-years in the 2–59 month age group, while pneumonia hospitalisations declined by 27% (95% CI 22–31). In the 5–14 year age group, IPD incidence declined by 69% (95% CI −28 to 91) and radiological pneumonia by 27% (95% CI −5 to 49).
Interpretation |
Routine introduction of PCV13 substantially reduced the incidence of childhood IPD and pneumonia in rural Gambia, including elimination of vaccine-type IPD in infants. Other low-income countries can expect substantial impact from the introduction of PCV13 using a schedule of three primary doses.
Funding |
Gavi, The Vaccine Alliance; Bill & Melinda Gates Foundation; UK Medical Research Council; Pfizer Ltd.
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Vol 21 - N° 9
P. 1293-1302 - septembre 2021 Retour au numéro
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