Evidence map›Paper›PMID 29211835›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2018

Massive Iatrogenic Outbreak of Human Immunodeficiency Virus Type 1 in Rural Cambodia, 2014-2015.

François Rouet, Janin Nouhin, Du-Ping Zheng, Benjamin Roche, Allison Black, Sophearot Prak, Marie Leoz, Catherine Gaudy-Graffin, Laurent Ferradini, Chandara Mom and 16 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

26 authors.

François RouetUnité Virus de l'Immunodéficience Humaine (VIH)/Hépatites, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Janin NouhinUnité Virus de l'Immunodéficience Humaine (VIH)/Hépatites, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Du-Ping ZhengInternational Laboratory Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.
Benjamin RocheUnité Mixte de Recherche Institut de Recherche pour le Développement 224, Centre National de la Recherche Scientifique 5290, Université de Montpellier, Maladies Infectieuses et Vecteurs: Ecologie, Génétique, Evolution et Contrôle, Montpellier, France.
Allison BlackFred Hutchinson Cancer Research Center, Seattle, Washington.
Sophearot PrakUnité Virus de l'Immunodéficience Humaine (VIH)/Hépatites, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Marie LeozCentre National de Référence sur le VIH, Laboratoire Associé, EA2656, Rouen University Hospital, Tours, France.
Catherine Gaudy-GraffinCentre National de Référence sur le VIH and Institut national de la santé et de la recherche médicale, Unité 966, Tours, France.
Laurent FerradiniWorld Health Organization, Phnom Penh, Cambodia.
Chandara MomNational Center for HIV/AIDS, Dermatology and Sexually Transmitted Diseases, Phnom Penh, Cambodia.
Sovatha MamNational Center for HIV/AIDS, Dermatology and Sexually Transmitted Diseases, Phnom Penh, Cambodia.
Charlotte GautierUnité Virus de l'Immunodéficience Humaine (VIH)/Hépatites, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Gérard LesageCentre National de Référence sur le VIH and Institut national de la santé et de la recherche médicale, Unité 966, Tours, France.
Sreymom KenUnité Virus de l'Immunodéficience Humaine (VIH)/Hépatites, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Kerya PhonUnité Virus de l'Immunodéficience Humaine (VIH)/Hépatites, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Alexandra KerleguerUnité Virus de l'Immunodéficience Humaine (VIH)/Hépatites, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Chunfu YangInternational Laboratory Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.
William KillamDivision of Global HIV/AIDS, Centers for Disease Control and Prevention, Phnom Penh, Cambodia.
Masami FujitaWorld Health Organization, Phnom Penh, Cambodia.
Chhivun MeanNational Center for HIV/AIDS, Dermatology and Sexually Transmitted Diseases, Phnom Penh, Cambodia.
Didier FontenilleUnité Virus de l'Immunodéficience Humaine (VIH)/Hépatites, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Francis BarinCentre National de Référence sur le VIH and Institut national de la santé et de la recherche médicale, Unité 966, Tours, France.
Jean-Christophe PlantierCentre National de Référence sur le VIH, Laboratoire Associé, EA2656, Rouen University Hospital, Tours, France.
Trevor BedfordFred Hutchinson Cancer Research Center, Seattle, Washington.
Artur RamosDivision of Global HIV/AIDS, Centers for Disease Control and Prevention, Phnom Penh, Cambodia.
Vonthanak SaphonnUniversity of Health Sciences, Phnom Penh, Cambodia.

Funding

FHCRC High-Performance Computing ClusterS10OD020069 · OD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KOOPERBERG, CHARLES L · 2015 to 2015
$600k
CGH CDC HHS U2G GH000989Intramural CDC HHS CC999999NIH HHS S10 OD020069World Health Organization 001
6 · The paper itself

Abstract

Background: In 2014-2015, 242 individuals aged 2-89 years were newly diagnosed with human immunodeficiency virus type 1 (HIV-1) in Roka, a rural commune in Cambodia. A case-control study attributed the outbreak to unsafe injections. We aimed to reconstruct the likely transmission history of the outbreak. Methods: We assessed in 209 (86.4%) HIV-infected cases the presence of hepatitis C virus (HCV) and hepatitis B virus (HBV). We identified recent infections using antibody (Ab) avidity testing for HIV and HCV. We performed amplification, sequencing, and evolutionary phylogenetic analyses of viral strains. Geographical coordinates and parenteral exposure through medical services provided by an unlicensed healthcare practitioner were obtained from 193 cases and 1499 controls during interviews. Results: Cases were coinfected with HCV (78.5%) and HBV (12.9%). We identified 79 (37.8%) recent (<130 days) HIV infections. Phylogeny of 202 HIV env C2V3 sequences showed a 198-sample CRF01_AE strains cluster, with time to most recent common ancestor (tMRCA) in September 2013 (95% highest posterior density, August 2012-July 2014), and a peak of 15 infections/day in September 2014. Three geospatial HIV hotspots were discernible in Roka and correlated with high exposure to the practitioner (P = .04). Fifty-nine of 153 (38.6%) tested cases showed recent (<180 days) HCV infections. Ninety HCV NS5B sequences formed 3 main clades, 1 containing 34 subtypes 1b with tMRCA in 2012, and 2 with 51 subtypes 6e and tMRCAs in 2002-2003. Conclusions: Unsafe injections in Cambodia most likely led to an explosive iatrogenic spreading of HIV, associated with a long-standing and more genetically diverse HCV propagation.

Indexed as

Disease OutbreaksAdolescentAdultAgedAged, 80 and overCambodiaCase-Control StudiesChildChild, PreschoolFemaleHIV-1HIV InfectionsHumansIatrogenic DiseaseInjectionsMale

Identifiers

PMID29211835
PMCPMC5963970

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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.