Evidence map›Paper›PMID 26625453›Full record

ArticleJournal of the Pediatric Infectious Diseases Society2014

Variation in Risk of Hospital-Onset Clostridium difficile Infection Across β-Lactam Antibiotics in Children With New-Onset Acute Lymphoblastic Leukemia.

Brian T Fisher, Julia Shaklee Sammons, Yimei Li, Peter de Blank, Alix E Seif, Yuan-Shung Huang, Marko Kavcic, Sarah Klieger, Tracey Harris, Kari Torp and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the Pediatric Infectious Diseases Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Recurrent community-acquired Clostridium(Clostridioides)difficile infection in Serbianchildren.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2020
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. TargetingFrontiers in microbiology · 2018
    Review
  9. Levofloxacin Prophylaxis During Induction Therapy for Pediatric Acute Lymphoblastic Leukemia.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2017
    Observational
  10. Article
  11. Review
  12. 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

13 authors at 5 institutions in 1 country.

Brian T FisherDivision of Infectious Diseases Center for Pediatric Clinical Effectiveness, The Children's Hospital of Philadelphia, Pennsylvania Department of Pediatrics, and Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Julia Shaklee SammonsDivision of Infectious Diseases Department of Infection Prevention and Control Center for Pediatric Clinical Effectiveness, The Children's Hospital of Philadelphia, Pennsylvania Department of Pediatrics, and.
Yimei LiDivision of Oncology, and Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Peter de BlankDivision of Pediatric Hematology and Oncology, Rainbow Babies & Children's Hospital Department of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Alix E SeifDivision of Oncology, and Department of Pediatrics, and.
Yuan-Shung HuangDepartment of Pediatrics, and.
Marko KavcicDivision of Oncology, and.
Sarah KliegerDivision of Infectious Diseases.
Tracey HarrisDivision of Oncology, and.
Kari TorpDivision of Oncology, and.
Douglas RheamDivision of Oncology, and.
Ami ShahDivision of Oncology, and.
Richard AplencDivision of Oncology, and Center for Pediatric Clinical Effectiveness, The Children's Hospital of Philadelphia, Pennsylvania Department of Pediatrics, and Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Pediatrics and Genetics · USUniversity of Pennsylvania · USCase Western Reserve University · USChildren's Hospital of Philadelphia · USOffice of Infectious Diseases · US

Funding

TRANSLATIONAL RESEARCH ONCOLOGY TRAINING GRANTK12CA076917 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI GERSON, STANTON L. · 1997 to 2022
$14.2M
Genetic Predictors of AML Treatment ResponseR01CA133881 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI APLENC, RICHARD · 2010 to 2014
$2.8M
Toxicity Monitoring on Phase III Trials with Administrative DataR01CA165277 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI APLENC, RICHARD · 2012 to 2015
$1.8M
NCI NIH HHS K12 CA076917NCI NIH HHS R01 CA133881NCI NIH HHS R01CA133881NCI NIH HHS R01 CA165277
6 · The paper itself

Abstract

backgroundAntibiotic exposure is common among children with leukemia. However, limited data exist regarding the risk of Clostridium difficile infection (CDI) across anti-pseudomonal β-lactam antibiotics commonly used for fever and neutropenia.

methodsA multicenter cohort of children with newly diagnosed acute lymphoblastic leukemia (ALL) was established from 43 freestanding children's hospitals from 1999 to 2009. Patients were followed until their index CDI event, defined by the CDI ICD-9 code plus a C difficile test charge, or until 180 days from ALL diagnosis. Cox proportional hazards models were performed to identify the hazards of CDI after exposure to anti-pseudomonal β-lactams, adjusting for demographics, other antibiotic exposures, severity of illness, antacids, gastrointestinal manipulation, and confounding by hospital.

resultsA cohort of 8268 ALL patients was assembled; median age was 5.5 years (interquartile range, 3.26-10.58). Two-hundred sixty-eight (3.2%) patients developed CDI within 180 days of ALL diagnosis. Each 1-day increase in exposure to an anti-pseudomonal β-lactam within the prior 30 days was associated with a significantly increased risk for CDI (hazard ratio [HR], 1.05; 95% confidence interval [CI], 1.01, 1.09). Ceftazidime (HR, 1.05; 95% CI, 1.02, 1.08) and cefepime (HR, 1.07; 95% CI, 1.02, 1.12) were each independently associated with CDI.

conclusionsEfforts to reduce total exposure to anti-pseudomonal β-lactam agents may help to reduce the risk of CDI in children with newly diagnosed ALL. Cefepime and ceftazidime were independently associated with CDI, whereas anti-pseudomonal penicillins and carbapenems were not. These findings, if confirmed, have potential implications for antibiotic choice during periods of fever and neutropenia.

Indexed as

Clostridium difficileleukemiapediatrics.

Identifiers

PMID26625453
PMCPMC4854370
OpenAlexW2141280144

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.