Evidence map›Paper›PMID 19563257›Full record

Trial reportThe Journal of infectious diseases2009

Ciprofloxacin dosage and emergence of resistance in human commensal bacteria.

Bruno Fantin, Xavier Duval, Laurent Massias, Loubna Alavoine, Françoise Chau, Sylvie Retout, Antoine Andremont, France Mentré

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00190151 (Pharmacokinetic/Pharmacodynamic Parameters Associated With the Emergence of Resistance to Ciprofloxacin in Human Commensal Flora), which is not on this map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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.

NCT00190151 naterminatednot on this map

Pharmacokinetic/Pharmacodynamic Parameters Associated With the Emergence of Resistance to Ciprofloxacin in Human Commensal Flora

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2004 to 2005Enrolled48ConditionsHealthy VolunteersArmsciprofloxacin
3 · Its place in the literature

Who cites it

48 citing papers in PubMed.

  1. Trial
  2. Protection of the Human Gut Microbiome From Antibiotics.The Journal of infectious diseases · 2018
    Trial
  3. Trial
  4. Review
  5. Review
  6. Liver Cyst Infection Outcomes in Patients With ADPKD.Kidney international reports · 2026
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. A Novel Non-Coding RNA CsiR Regulates the Ciprofloxacin Resistance inInternational journal of molecular sciences · 2021
    Article
  16. Article
  17. The Gut Microbiome as a Reservoir for Antimicrobial Resistance.The Journal of infectious diseases · 2021
    Review
  18. Review
  19. Article
  20. 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

8 authors.

Bruno FantinUniversité Paris Diderot, Paris, France. bruno.fantin@bjn.aphp.fr
Xavier Duval
Laurent Massias
Loubna Alavoine
Françoise Chau
Sylvie Retout
Antoine Andremont
France Mentré

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough optimization of the fluoroquinolone dosage increases the efficacy of this class of drugs against bacterial infections, its impact on the emergence of resistance in commensal bacteria is unknown.

methodsSix different 14-day dosages of oral ciprofloxacin were randomly assigned to 48 healthy volunteers. Individual pharmacokinetic and pharmacodynamic parameters combining antibiotic exposure in plasma, saliva, and stool specimens and ciprofloxacin minimum inhibitory concentrations (MICs) and mutant prevention concentrations against viridans group streptococci in the pharyngeal flora and Escherichia coli in the fecal flora were estimated. Their links with the emergence of resistance to nalidixic acid or ciprofloxacin in the fecal flora and to levofloxacin in the pharyngeal flora 7, 14, or 42 days after ciprofloxacin initiation were investigated.

resultsResistance emerged in the fecal and pharyngeal flora of 25% and 33% of the subjects, respectively, mainly when local concentrations of ciprofloxacin were less than the MIC. No variable that integrated pharmacokinetic data and pharmacodynamic parameters was found to differ significantly between the subjects in whom resistance emerged and those in whom it did not. Probabilities of the emergence of resistance were not significantly different across the different antibiotic dosages.

conclusionsSelection of resistant commensals during ciprofloxacin therapy is a frequent ecological side effect that is not preventable by dosage optimization. Trial registration. Clinical Trials.gov identifier: NCT00190151.

Indexed as

Drug Resistance, BacterialAdultAnti-Bacterial AgentsCiprofloxacinEscherichia coliFecesFemaleHumansMaleMicrobial Sensitivity TestsPharynxSalivaViridans StreptococciYoung AdultAnti-Bacterial AgentsCiprofloxacin

Identifiers

PMID19563257
PMCPMC2933399

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.