Evidence map›Paper›PMID 27223476›Full record

ArticlePloS one2016

Molecular Epidemiology and Clinical Impact of Acinetobacter calcoaceticus-baumannii Complex in a Belgian Burn Wound Center.

Daniel De Vos, Jean-Paul Pirnay, Florence Bilocq, Serge Jennes, Gilbert Verbeken, Thomas Rose, Elkana Keersebilck, Petra Bosmans, Thierry Pieters, Mony Hing and 11 more

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–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

19 citing papers in PubMed.

  1. Microbiology spectrum · 2024
    Article
  2. Characterization of a colistin resistant, hypervirulent hospital isolate of Acinetobacter courvalinii from Canada.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2024
    Article
  3. AN OUTBREAK OF EXTENSIVELY DRUG-RESISTANTAnnals of burns and fire disasters · 2024
    Article
  4. Review
  5. Article
  6. Molecular Epidemiology of Clinical Carbapenem-ResistantTropical medicine and infectious disease · 2022
    Article
  7. The Specific Capsule Depolymerase of Phage PMK34 SensitizesAntibiotics (Basel, Switzerland) · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Lysin LysMK34 ofApplied and environmental microbiology · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Extensive colonization with carbapenemase-producing microorganisms in Romanian burn patients: infectious consequences from the Colectiv fire disaster.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2018
    Article
  16. Article
  17. Article
  18. Predicting and managing sepsis in burn patients: current perspectives.Therapeutics and clinical risk management · 2017
    Article
  19. 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

21 authors.

Daniel De VosLaboratory for Molecular and Cellular Technology, Queen Astrid Military Hospital, Brussels, Belgium.
Jean-Paul PirnayLaboratory for Molecular and Cellular Technology, Queen Astrid Military Hospital, Brussels, Belgium.
Florence BilocqLaboratory for Molecular and Cellular Technology, Queen Astrid Military Hospital, Brussels, Belgium.
Serge JennesBurn Wound Center, Queen Astrid Military Hospital, Brussels, Belgium.
Gilbert VerbekenLaboratory for Molecular and Cellular Technology, Queen Astrid Military Hospital, Brussels, Belgium.
Thomas RoseBurn Wound Center, Queen Astrid Military Hospital, Brussels, Belgium.
Elkana KeersebilckBurn Wound Center, Queen Astrid Military Hospital, Brussels, Belgium.
Petra BosmansHospital Hygiene and Infection Control Team, Queen Astrid Military Hospital, Brussels, Belgium.
Thierry PietersHospital Hygiene and Infection Control Team, Queen Astrid Military Hospital, Brussels, Belgium.
Mony HingClinical Laboratory, Queen Astrid Military Hospital, Brussels, Belgium.
Walter HeuninckxClinical Laboratory, Queen Astrid Military Hospital, Brussels, Belgium.
Frank De PauwMedical Communication and Information Systems, ACOS WB/Health Division, Queen Astrid Military Hospital, Brussels, Belgium.
Patrick SoentjensBurn Wound Center, Queen Astrid Military Hospital, Brussels, Belgium.
Maia MerabishviliLaboratory for Molecular and Cellular Technology, Queen Astrid Military Hospital, Brussels, Belgium.
Pieter DeschaghtLaboratory Bacteriology Research, University of Ghent, Ghent, Belgium.
Mario VaneechoutteLaboratory Bacteriology Research, University of Ghent, Ghent, Belgium.
Pierre BogaertsLaboratoire de Bactériologie, CHU Mont-Godinne, Université Catholique de Louvain, Yvoir, Belgium.
Youri GlupczynskiLaboratoire de Bactériologie, CHU Mont-Godinne, Université Catholique de Louvain, Yvoir, Belgium.
Bruno PotApplied Maths, Sint-Martens-Latem, Belgium.
Tanny J van der ReijdenDepartment of Infectious Diseases C5-P, Leiden University Medical Center, Leiden, The Netherlands.
Lenie DijkshoornDepartment of Infectious Diseases C5-P, Leiden University Medical Center, Leiden, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multidrug resistant Acinetobacter baumannii and its closely related species A. pittii and A. nosocomialis, all members of the Acinetobacter calcoaceticus-baumannii (Acb) complex, are a major cause of hospital acquired infection. In the burn wound center of the Queen Astrid military hospital in Brussels, 48 patients were colonized or infected with Acb complex over a 52-month period. We report the molecular epidemiology of these organisms, their clinical impact and infection control measures taken. A representative set of 157 Acb complex isolates was analyzed using repetitive sequence-based PCR (rep-PCR) (DiversiLab) and a multiplex PCR targeting OXA-51-like and OXA-23-like genes. We identified 31 rep-PCR genotypes (strains). Representatives of each rep-type were identified to species by rpoB sequence analysis: 13 types to A. baumannii, 10 to A. pittii, and 3 to A. nosocomialis. It was assumed that isolates that belonged to the same rep-type also belonged to the same species. Thus, 83.4% of all isolates were identified to A. baumannii, 9.6% to A. pittii and 4.5% to A. nosocomialis. We observed 12 extensively drug resistant Acb strains (10 A. baumannii and 2 A. nosocomialis), all carbapenem-non-susceptible/colistin-susceptible and imported into the burn wound center through patients injured in North Africa. The two most prevalent rep-types 12 and 13 harbored an OXA-23-like gene. Multilocus sequence typing allocated them to clonal complex 1 corresponding to EU (international) clone I. Both strains caused consecutive outbreaks, interspersed with periods of apparent eradication. Patients infected with carbapenem resistant A. baumannii were successfully treated with colistin/rifampicin. Extensive infection control measures were required to eradicate the organisms. Acinetobacter infection and colonization was not associated with increased attributable mortality.

Indexed as

Acinetobacter baumanniiAcinetobacter calcoaceticusAcinetobacter InfectionsAdolescentAdultAfrica, NorthernAgedAged, 80 and overBacterial Typing TechniquesBelgiumBurnsChildChild, PreschoolColistinDrug Resistance, BacterialFemaleColistinRNA, BacterialRNA, Ribosomal, 16S

Identifiers

PMID27223476
PMCPMC4880317

What OpenQuestion holds

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LicenceCC BY
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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.