Evidence map›Paper›PMID 36907733›Full record

ArticleVaccine2023

Vaccine-derived poliovirus serotype 2 outbreaks and response in the Democratic Republic of the Congo, 2017-2021.

Mary M Alleman, Jaume Jorba, Yogolelo Riziki, Elizabeth Henderson, Anicet Mwehu, Lerato Seakamela, Wayne Howard, Albert Kadiobo Mbule, Renee Ntumbannji Nsamba, Kpandja Djawe and 7 more

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 5 institutions in 4 countries.

Mary M AllemanGlobal Immunization Division, Centers for Disease Control and Prevention, Atlanta, USA. Electronic address: mea4@cdc.gov.
Jaume JorbaDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, USA.
Yogolelo RizikiInstitut National de Recherche Biomédicale, Ministry of Public Health, Hygiene and Prevention, Democratic Republic of the Congo.
Elizabeth HendersonDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, USA.
Anicet MwehuEmergency Operations Center for Polio, Ministry of Public Health, Hygiene and Prevention, Democratic Republic of the Congo.
Lerato SeakamelaNational Institute for Communicable Diseases, National Health Laboratory Services, South Africa.
Wayne HowardNational Institute for Communicable Diseases, National Health Laboratory Services, South Africa.
Albert Kadiobo MbulePolio, Office of the Regional Director, World Health Organization, Democratic Republic of the Congo Country Office, Democratic Republic of the Congo.
Renee Ntumbannji NsambaPolio, Office of the Regional Director, World Health Organization, Democratic Republic of the Congo Country Office, Democratic Republic of the Congo.
Kpandja DjawePolio, Office of the Regional Director, World Health Organization, Democratic Republic of the Congo Country Office, Democratic Republic of the Congo.
Moïse Désiré YapiPolio, Office of the Regional Director, World Health Organization, Democratic Republic of the Congo Country Office, Democratic Republic of the Congo.
Marcellin Nimpa MengouoPolio, Office of the Regional Director, World Health Organization, Democratic Republic of the Congo Country Office, Democratic Republic of the Congo.
Nicksy GumedePolio, Office of the Regional Director, World Health Organization, Regional Office for Africa, Republic of the Congo.
Modjirom NdoutabePolio, Office of the Regional Director, World Health Organization, Regional Office for Africa, Republic of the Congo.
Anfumbom K W KfutwahPolio, Office of the Regional Director, World Health Organization, Regional Office for Africa, Republic of the Congo.
Kamel SenouciBill and Melinda Gates Foundation, Washington, USA.
Cara C BurnsDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, USA.
World Health Organization Regional Office for Africa · CGCenters for Disease Control and Prevention · USMinistry of Public Health · CDNational Health Laboratory Service · ZABill & Melinda Gates Foundation · US

Funding

Intramural CDC HHS CC999999World Health Organization 001
6 · The paper itself

Abstract

Vaccine-derived polioviruses (VDPVs) can emerge from Sabin strain poliovirus serotypes 1, 2, and 3 contained in oral poliovirus vaccine (OPV) after prolonged person-to-person transmission where population vaccination immunity against polioviruses is suboptimal. VDPVs can cause paralysis indistinguishable from wild polioviruses and outbreaks when community circulation ensues. VDPV serotype 2 outbreaks (cVDPV2) have been documented in The Democratic Republic of the Congo (DRC) since 2005. The nine cVDPV2 outbreaks detected during 2005-2012 were geographically-limited and resulted in 73 paralysis cases. No outbreaks were detected during 2013-2016. During January 1, 2017-December 31, 2021, 19 cVDPV2 outbreaks were detected in DRC. Seventeen of the 19 (including two first detected in Angola) resulted in 235 paralysis cases notified in 84 health zones in 18 of DRC's 26 provinces; no notified paralysis cases were associated with the remaining two outbreaks. The DRC-KAS-3 cVDPV2 outbreak that circulated during 2019-2021, and resulted in 101 paralysis cases in 10 provinces, was the largest recorded in DRC during the reporting period in terms of numbers of paralysis cases and geographic expanse. The 15 outbreaks occurring during 2017-early 2021 were successfully controlled with numerous supplemental immunization activities (SIAs) using monovalent OPV Sabin-strain serotype 2 (mOPV2); however, suboptimal mOPV2 vaccination coverage appears to have seeded the cVDPV2 emergences detected during semester 2, 2018 through 2021. Use of the novel OPV serotype 2 (nOPV2), designed to have greater genetic stability than mOPV2, should help DRC's efforts in controlling the more recent cVDPV2 outbreaks with a much lower risk of further seeding VDPV2 emergence. Improving nOPV2 SIA coverage should decrease the number of SIAs needed to interrupt transmission. DRC needs the support of polio eradication and Essential Immunization (EI) partners to accelerate the country's ongoing initiatives for EI strengthening, introduction of a second dose of inactivated poliovirus vaccine (IPV) to increase protection against paralysis, and improving nOPV2 SIA coverage.

Indexed as

PoliomyelitisPoliovirusDemocratic Republic of the CongoDisease OutbreaksHumansPoliovirus Vaccine, OralSerogroupPoliovirus Vaccine, OralAcute flaccid paralysisAfricaCirculating vaccine-derived poliovirus type 2Democratic Republic of the CongoMonovalent oral polio vaccine type 2Novel oral polio vaccine type 2Polio eradicationPoliovirus environmental surveillancePoliovirus outbreak responseSupplemental immunization activitiesSurveillance

Identifiers

PMID36907733
PMCPMC10427717
OpenAlexW4323922614

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.