Evidence map›Paper›PMID 25267108›Full record

ArticleBMC infectious diseases2014

Clostridium difficile carriage in hospitalized cancer patients: a prospective investigation in eastern China.

Wei-Jia Fang, Da-Zhi Jing, Yun Luo, Cai-Yun Fu, Peng Zhao, Jiong Qian, Bing-Ru Tian, Xiao-Gang Chen, Yu-Long Zheng, Yi Zheng and 6 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
2.2field-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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  14. Nagging Presence ofJournal of clinical and diagnostic research : JCDR · 2017
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  19. Review
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

16 authors at 5 institutions in 1 country.

Wei-Jia Fang
Da-Zhi Jing
Yun Luo
Cai-Yun Fu
Peng Zhao
Jiong Qian
Bing-Ru Tian
Xiao-Gang Chen
Yu-Long Zheng
Yi Zheng
Jing Deng
Wei-Hua Zou
Xue-Ren Feng
Fan-Long Liu
Xiao-Zhou Mou
Shu-Sen ZhengFirst Affiliated Hospital, School of Medicine, ZheJiang University, 79 Qinchun Road, Hangzhou 310006, China. shusenzheng@zju.edu.cn.
Zhejiang University · CNHuzhou Central Hospital · CNZhejiang Center for Disease Control and Prevention · CNZhejiang Provincial People's Hospital · CNZhejiang Sci-Tech University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClostridium difficile carriage has been considered as a potential source for the deadly infection, but its role in cancer patients is still unclear. We aimed to identify the clinical and immunological factors that are related to C. difficile carriage in Chinese cancer patients.

methodsA total of 400 stool samples were collected from cancer patients who received chemotherapy in three hospitals of eastern China. Bacterial genomic DNA was extracted and two toxin genes (tcdA and tcdB) were detected. PCR ribotyping was performed using capillary gel electrophoresis. Concentrations of prostaglandin E2 (PGE2), transforming growth factor beta (TGF-β) and interleukin-10 (IL-10) were measured using enzyme-linked immunosorbent assay (ELISA) kits.

resultsEighty-two (20.5%) samples were confirmed to be C. difficile-positive and positive for tpi, tcdA, and tcdB genes. The C. difficile-positive rates in patients with diarrhea and no diarrhea were 35% and 19.7%, respectively (p = 0.09). Patients who were younger than 50 years old and were hospitalized for at least 10 days had a C. difficile-positive rate as high as 35%. In contrast, patients who were older than 50 years old and were hospitalized for less than 10 days had a C. difficile-positive rate of only 12.7% (p = 0.0009). No association was found between C. difficile carriage and chemotherapy regimen, antibiotic drug use, or immunosuppressive mediators, such as prostaglandin E2 (PGE2), transforming growth factor beta (TGF-β), or interleukin-10 (IL-10). Twelve ribotypes of C. difficile were identified, but none of them belonged to ribotype 027.

conclusionsWe conclude that younger patients and those with longer hospitalization stays may be more prone to C. difficile carriage. Studies of larger populations are warranted to clarify the exact role of C. difficile carriage in hospitalized cancer patients in China.

Indexed as

Bacterial ToxinsCarrier StateChinaClostridioides difficileDiarrheaDNA, BacterialEnterocolitis, PseudomembranousEnzyme-Linked Immunosorbent AssayFemaleHospitalizationHumansInterleukin-10MaleMiddle AgedMolecular Diagnostic TechniquesNeoplasmsBacterial ToxinsDNA, BacterialInterleukin-10

Identifiers

PMID25267108
PMCPMC4261591
OpenAlexW2000787993

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.