Evidence map›Paper›PMID 33783664›Full record

Observational studyEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2021

Predictive factors, outcomes, and molecular epidemiology of Clostridioides difficile diarrhea in Brazilian hospitals.

Evelyne Santana Girão, Bruno de Melo Tavares, Sania Alves Dos Santos, Gessica Lorena Gamarra, Camila Rizek, Roberta Cristina Martins, Lauro Vieira Perdigão Neto, Constancia Diogo, Tatiana D' Annibale Orsi, Hugo Manuel Paz Morales and 11 more

Abstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. High genetic similarity betweenFrontiers in public health · 2025
    Article
  2. Article
  3. Article
  4. Review
  5. Metronidazole for Treatment ofAntibiotics (Basel, Switzerland) · 2022
    Article
  6. 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 at 4 institutions in 1 country.

Evelyne Santana GirãoHospital Universitário Walter Cantídio, Universidade Federal do Ceará, R. Pastor Samuel Munguba, 1290 - Rodolfo Teófilo, Fortaleza, Ceará, 60430-372, Brazil. egirao@uol.com.br.ORCID http://orcid.org/0000-0003-3059-5490
Bruno de Melo TavaresDivisão de Moléstias Infecciosas, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Sania Alves Dos SantosLIM-49, Instituto de Medicina Tropical, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Gessica Lorena GamarraLIM-49, Instituto de Medicina Tropical, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Camila RizekLIM-49, Instituto de Medicina Tropical, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Roberta Cristina MartinsLIM-49, Instituto de Medicina Tropical, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Lauro Vieira Perdigão NetoDivisão de Moléstias Infecciosas, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Constancia DiogoLIM-49, Instituto de Medicina Tropical, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Tatiana D' Annibale OrsiLIM-49, Instituto de Medicina Tropical, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Hugo Manuel Paz MoralesHospital das Clínicas, Universidade Federal do Paraná, Curitiba, Brazil.
Keite da Silva NogueiraHospital das Clínicas, Universidade Federal do Paraná, Curitiba, Brazil.
Adriane Ceshin MaestriHospital das Clínicas, Universidade Federal do Paraná, Curitiba, Brazil.
Icaro BoszczowskiDivisão de Moléstias Infecciosas, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Filipe PiastrelliHospital Alemão Oswaldo Cruz, São Paulo, Brazil.
Cecilia Leite CostaDepartamento de Morfologia, Universidade Federal do Ceará, Fortaleza, Brazil.
Daniely Viana CostaHospital Universitário Walter Cantídio, Universidade Federal do Ceará, R. Pastor Samuel Munguba, 1290 - Rodolfo Teófilo, Fortaleza, Ceará, 60430-372, Brazil.
Geovania MacielHospital Universitário Walter Cantídio, Universidade Federal do Ceará, R. Pastor Samuel Munguba, 1290 - Rodolfo Teófilo, Fortaleza, Ceará, 60430-372, Brazil.
Janete RomãoHospital São José de Doenças Infecciosas, Fortaleza, Brazil.
Thais GuimarãesDivisão de Moléstias Infecciosas, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Gerly Anne de Castro BritoDepartamento de Morfologia, Universidade Federal do Ceará, Fortaleza, Brazil.
Silvia Figueiredo CostaDivisão de Moléstias Infecciosas, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRUniversidade Federal do Ceará · BRHospital de Clínicas Universidade Federal do Paraná · BRHospital Alemão Oswaldo Cruz · BR

Funding

Instituto Científico Pfizer 53233563
6 · The paper itself

Abstract

Little is known about the role of lineage of strains of Clostridioides difficile (CD) on the clinical presentation of CD infection (CDI) in Latin America, especially regarding the treatment response. We conducted a multicenter, prospective study to investigate the predictive factors and treatment outcomes of CDI in hospitalized patients and to performed phenotypical and molecular characterization of CD strains. A total of 361 diarrheic patients at 5 hospitals from different regions of the country were enrolled. All stool samples were tested for glutamate dehydrogenase (GDH), toxins A and B, and toxin genes using a nucleic acid amplification test (NAAT). Specimens were cultured and susceptibility profile and whole-genome sequencing (WGS) were performed. CDI positivity was 15% (56/377). Predictive factors for CDI were prior use of meropenem (OR 4.09, 95% CI 2.097-7.095; p<0.001), mucus in stools (OR 3.29; 95% CI 1.406-7.722; p=0.006) and neutrophil left-shift with >20% of bands (OR 3.77; 95% IC 1.280-11.120; p=0.016). Overall mortality was 19%, with no deaths attributed to CDI. Oral metronidazole was used in 74% of cases, with 85% of cure and 14% of recurrence. A total of 35 CD isolates were recovered, all of them susceptible to metronidazole and vancomycin. The WGS revealed 17 different STs, six of which were novel. ST42 was the most common ST and hypervirulent strains were not found. Severe CDI were caused by ST42, ST5, ST8, ST48, ST33 and a novel ST667. The ermB gene was more frequently found in isolates of ST42 (p=0.004).

Indexed as

AdultAgedAnti-Bacterial AgentsBacterial ProteinsBrazilClostridioides difficileClostridium InfectionsDiarrheaDNA, BacterialFecesFemaleHospitalizationHumansMaleMiddle AgedProspective StudiesAnti-Bacterial AgentsBacterial ProteinsDNA, BacterialClostridioides difficileDiarrheaPredictive factors, Metronidazole, Molecular epidemiology

Identifiers

PMID33783664
OpenAlexW3139791082

What OpenQuestion holds

Textmetadata
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.