Evidence map›Paper›PMID 26629031›Full record

ArticleInternational journal of clinical and experimental medicine2015

In vitro drug susceptibility of 40 international reference rapidly growing mycobacteria to 20 antimicrobial agents.

Hui Pang, Guilian Li, Li Wan, Yi Jiang, Haican Liu, Xiuqin Zhao, Zhongfu Zhao, Kanglin Wan

Abstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Dual Infection of an Open Fracture Caused byAntibiotics (Basel, Switzerland) · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Mycobacterium abscessus drug discovery using machine learning.Tuberculosis (Edinburgh, Scotland) · 2022
    Article
  8. Article
  9. Article
  10. Rifabutin Is Active against Mycobacterium abscessus Complex.Antimicrobial agents and chemotherapy · 2017
    Article
  11. Draft Genome Sequence ofGenome announcements · 2017
    Article
  12. Article
  13. Treatment of Non-Tuberculous Mycobacterial Lung Disease.Current treatment options in infectious diseases · 2016
    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.

Hui PangDepartment of Immunology, Changzhi Medical College Changzhi 046000, Shanxi, China ; State Key Laboratory of Infectious Diseases Prevention and Control, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention & National Tuberculosis Reference Laboratory Beijing 102206, China ; Department of Immunology, Xiangya School of Medicine, Central South University Changsha 410078, Hunan, China.
Guilian LiState Key Laboratory of Infectious Diseases Prevention and Control, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention & National Tuberculosis Reference Laboratory Beijing 102206, China ; Department of Physiology, Xiangya School of Medicine, Central South University Changsha 410078, Hunan, China.
Li WanDepartment of Physiology, Xiangya School of Medicine, Central South University Changsha 410078, Hunan, China.
Yi JiangState Key Laboratory of Infectious Diseases Prevention and Control, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention & National Tuberculosis Reference Laboratory Beijing 102206, China.
Haican LiuState Key Laboratory of Infectious Diseases Prevention and Control, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention & National Tuberculosis Reference Laboratory Beijing 102206, China.
Xiuqin ZhaoState Key Laboratory of Infectious Diseases Prevention and Control, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention & National Tuberculosis Reference Laboratory Beijing 102206, China.
Zhongfu ZhaoInstitute of Hepatology of Changzhi Medical College Changzhi 046000, Shanxi, China.
Kanglin WanState Key Laboratory of Infectious Diseases Prevention and Control, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention & National Tuberculosis Reference Laboratory Beijing 102206, China ; Department of Physiology, Xiangya School of Medicine, Central South University Changsha 410078, Hunan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rapidly growing mycobacteria (RGM) are human pathogens that are relatively easily identified by acid-fast staining but are proving difficult to treat in the clinic. In this study, we performed susceptibility testing of 40 international reference RGM species against 20 antimicrobial agents using the cation-adjusted Mueller-Hinton (CAMH) broth microdilution based on the minimum inhibitory concentration (MIC) assay recommended by the guidelines of the Clinical and Laboratory Standards Institute (CLSI). The results demonstrated that RGM organisms were resistant to the majority of first-line antituberculous agents but not to second-line fluoroquinolones or aminoglycosides. Three drugs (amikacin, tigecycline and linezolid) displayed potent antimycobacterial activity against all tested strains. Capreomycin, levofloxacin and moxifloxacin emerged as promising candidates for the treatment of RGM infections, and cefoxitin and meropenem were active against most strains. Mycobacterium chelonae (M. chelonae), M. abscessus, M. bolletii, M. fortuitum, M. boenickei, M. conceptionense, M. pseudoshottsii, M. septicum and M. setense were the most resistant RGM species. These results provide significant insight into the treatment of RGM species and will assist optimization of clinical criteria.

Indexed as

antimicrobialDrug susceptibilityminimum inhibitory concentration (MIC)rapidly growing mycobacteria (RGM)reference strains

Identifiers

PMID26629031
PMCPMC4658920

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.