Evidence map›Paper›PMID 38485142›Full record

ArticleBMJ global health2024

African polyvalent antivenom can maintain pharmacological stability and ability to neutralise murine venom lethality for decades post-expiry: evidence for increasing antivenom shelf life to aid in alleviating chronic shortages.

Gabriela Solano, Sinead Cunningham, Rebecca J Edge, Gina Duran, Adriana Sanchez, Mauren Villalta, Rachel H Clare, Mark C Wilkinson, Amy E Marriott, Camille Abada and 8 more

Open access · goldAbstract read
In one paragraph

Article in BMJ global health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
6.6field-weighted citation impact, top 3% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
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

18 authors at 4 institutions in 4 countries.

Gabriela SolanoInstituto Clodomiro Picado, Universidad de Costa Rica, San Jose, Costa Rica.
Sinead CunninghamLiverpool School of Tropical Medicine, Liverpool, UK.
Rebecca J EdgeLiverpool School of Tropical Medicine, Liverpool, UK.
Gina DuranInstituto Clodomiro Picado, Universidad de Costa Rica, San Jose, Costa Rica.
Adriana SanchezInstituto Clodomiro Picado, Universidad de Costa Rica, San Jose, Costa Rica.
Mauren VillaltaInstituto Clodomiro Picado, Universidad de Costa Rica, San Jose, Costa Rica.
Rachel H ClareLiverpool School of Tropical Medicine, Liverpool, UK.
Mark C WilkinsonLiverpool School of Tropical Medicine, Liverpool, UK.
Amy E MarriottLiverpool School of Tropical Medicine, Liverpool, UK.
Camille AbadaLiverpool School of Tropical Medicine, Liverpool, UK.
Stefanie K MenziesLiverpool School of Tropical Medicine, Liverpool, UK.
Molly KeenLiverpool School of Tropical Medicine, Liverpool, UK.
David G LallooLiverpool School of Tropical Medicine, Liverpool, UK.
Ymkje StienstraLiverpool School of Tropical Medicine, Liverpool, UK.
Michael AbouyannisLiverpool School of Tropical Medicine, Liverpool, UK.
Nicholas R CasewellLiverpool School of Tropical Medicine, Liverpool, UK.
Guillermo LeónInstituto Clodomiro Picado, Universidad de Costa Rica, San Jose, Costa Rica.
Stuart AinsworthLiverpool School of Tropical Medicine, Liverpool, UK stuart.ainsworth@liverpool.ac.uk.ORCID http://orcid.org/0000-0002-0199-6482
Liverpool School of Tropical Medicine · GBUniversidad de Costa Rica · CRUniversity of Liverpool · GBUniversity of Groningen · NL

Funding

Wellcome Trust
6 · The paper itself

Abstract

introductionAntivenom is a lifesaving medicine for treating snakebite envenoming, yet there has been a crisis in antivenom supply for many decades. Despite this, substantial quantities of antivenom stocks expire before use. This study has investigated whether expired antivenoms retain preclinical quality and efficacy, with the rationale that they could be used in emergency situations when in-date antivenom is unavailable.

methodsUsing WHO guidelines and industry test requirements, we examined the in vitro stability and murine in vivo efficacy of eight batches of the sub-Saharan African antivenom, South African Institute for Medical Research polyvalent, that had expired at various times over a period of 30 years.

resultsWe demonstrate modest declines in immunochemical stability, with antivenoms older than 25 years having high levels of turbidity. In vitro preclinical analysis demonstrated all expired antivenoms retained immunological recognition of venom antigens and the ability to inhibit key toxin families. All expired antivenoms retained comparable in vivo preclinical efficacy in preventing the lethal effects of envenoming in mice versus three regionally and medically important venoms.

conclusionsThis study provides strong rationale for stakeholders, including manufacturers, regulators and health authorities, to explore the use of expired antivenom more broadly, to aid in alleviating critical shortages in antivenom supply in the short term and the extension of antivenom shelf life in the longer term.

Indexed as

AntiveninsSnake BitesAnimalsHumansMiceVenomsAntiveninsVenomsSnake bite, stings and other envenoming

Identifiers

PMID38485142
PMCPMC10941113
OpenAlexW4392820473

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.