Evidence map›Paper›PMID 26897105›Full record

ArticleThe Lancet. Infectious diseases2016

Effect of the introduction of pneumococcal conjugate vaccination on invasive pneumococcal disease in The Gambia: a population-based surveillance study.

Grant A Mackenzie, Philip C Hill, David J Jeffries, Ilias Hossain, Uchendu Uchendu, David Ameh, Malick Ndiaye, Oyedeji Adeyemi, Jayani Pathirana, Yekini Olatunji and 32 more

Open access · hybridAbstract read
In one paragraph

Article in The Lancet. Infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed, 5 pooled it
18.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

114 citing papers in PubMed, 5 syntheses or guidelines pooled it, 184 citations in OpenAlex.

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54 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

42 authors at 8 institutions in 7 countries.

Grant A MackenzieMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia; Murdoch Childrens Research Institute, Parkville, Melbourne, Australia; London School of Hygiene & Tropical Medicine, London, UK. Electronic address: gmackenzie@mrc.gm.
Philip C HillCentre for International Health, University of Otago, Dunedin, New Zealand.
David J JeffriesMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Ilias HossainMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Uchendu UchenduMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
David AmehMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Malick NdiayeMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Oyedeji AdeyemiMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Jayani PathiranaMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Yekini OlatunjiMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Bade AbatanMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Bilquees S MuhammadMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Augustin E FombahMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Debasish SahaMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Ian PlumbMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Aliu AkanoThe National Hospital, Central Area, Garki, Abuja, Nigeria.
Bernard EbrukeMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Readon C IdehMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Bankole KutiMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Peter GithuaMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Emmanuel OlutundeMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Ogochukwu OfordileMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Edward GreenMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Effua UsufMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Henry BadjiMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Usman N A IkumapayiMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Ahmad ManjangMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Rasheed SalaudeenMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
E David NsekpongMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Sheikh JarjuMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Martin AntonioMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia; London School of Hygiene & Tropical Medicine, London, UK; Warwick Medical School, University of Warwick, Coventry, UK.
Sana SambouMinistry of Health and Social Welfare, Gambia Government, Kotu, The Gambia.
Lamin CeesayMinistry of Health and Social Welfare, Gambia Government, Kotu, The Gambia.
Yamundow Lowe-JallowMinistry of Health and Social Welfare, Gambia Government, Kotu, The Gambia.
Momodou JassehMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
Kim MulhollandMurdoch Childrens Research Institute, Parkville, Melbourne, Australia; London School of Hygiene & Tropical Medicine, London, UK.
Maria KnollBloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA.
Orin S LevineBloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA.
Stephen R HowieMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia; Centre for International Health, University of Otago, Dunedin, New Zealand; Department of Paediatrics: Child and Youth Health, University of Auckland, Auckland, New Zealand.
Richard A AdegbolaGlaxoSmithKline Vaccines, Wavre, Belgium.
Brian M GreenwoodLondon School of Hygiene & Tropical Medicine, London, UK.
Tumani CorrahMedical Research Council, The Gambia Unit, Atlantic Road, Fajara, The Gambia.
MRC Unit the Gambia · GMMinistry of Health and Social Welfare · GMJohns Hopkins University · USLondon School of Hygiene & Tropical Medicine · GBUniversity of Otago · NZGlaxoSmithKline (Belgium) · BENational Hospital Abuja · NGUniversity of Warwick · GB

Funding

Medical Research Council MC_U190074190Medical Research Council MC_U190081991Medical Research Council MC_U190088478Medical Research Council MC_UP_1003/1Medical Research Council MC_UP_A900_1124
6 · The paper itself

Abstract

backgroundLittle information is available about the effect of pneumococcal conjugate vaccines (PCVs) in low-income countries. We measured the effect of these vaccines on invasive pneumococcal disease in The Gambia where the 7-valent vaccine (PCV7) was introduced in August, 2009, followed by the 13-valent vaccine (PCV13) in May, 2011.

methodsWe conducted population-based surveillance for invasive pneumococcal disease in individuals aged 2 months and older who were residents of the Basse Health and Demographic Surveillance System (BHDSS) in the Upper River Region, The Gambia, using standardised criteria to identify and investigate patients. Surveillance was done between May, 2008, and December, 2014. We compared the incidence of invasive pneumococcal disease between baseline (May 12, 2008-May 11, 2010) and after the introduction of PCV13 (Jan 1, 2013-Dec 31, 2014), adjusting for changes in case ascertainment over time.

findingsWe investigated 14 650 patients, in whom we identified 320 cases of invasive pneumococcal disease. Compared with baseline, after the introduction of the PCV programme, the incidence of invasive pneumococcal disease decreased by 55% (95% CI 30-71) in the 2-23 months age group, from 253 to 113 per 100 000 population. This decrease was due to an 82% (95% CI 64-91) reduction in serotypes covered by the PCV13 vaccine. In the 2-4 years age group, the incidence of invasive pneumococcal disease decreased by 56% (95% CI 25-75), from 113 to 49 cases per 100 000, with a 68% (95% CI 39-83) reduction in PCV13 serotypes. The incidence of non-PCV13 serotypes in children aged 2-59 months increased by 47% (-21 to 275) from 28 to 41 per 100 000, with a broad range of serotypes. The incidence of non-pneumococcal bacteraemia varied little over time.

interpretationThe Gambian PCV programme reduced the incidence of invasive pneumococcal disease in children aged 2-59 months by around 55%. Further surveillance is needed to ascertain the maximum effect of the vaccine in the 2-4 years and older age groups, and to monitor serotype replacement. Low-income and middle-income countries that introduce PCV13 can expect substantial reductions in invasive pneumococcal disease.

fundingGAVI's Pneumococcal vaccines Accelerated Development and Introduction Plan (PneumoADIP), Bill & Melinda Gates Foundation, and the UK Medical Research Council.

Indexed as

Population SurveillanceChild, PreschoolFemaleGambiaHeptavalent Pneumococcal Conjugate VaccineHumansImmunologic FactorsInfantMalePneumococcal InfectionsPneumococcal VaccinesStreptococcus pneumoniaeVaccinationVaccines, Conjugate13-valent pneumococcal vaccineHeptavalent Pneumococcal Conjugate VaccineImmunologic FactorsPneumococcal VaccinesVaccines, Conjugate

Identifiers

PMID26897105
PMCPMC4909992
OpenAlexW2283730606

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.