Evidence map›Paper›PMID 12364376›Full record

ReviewClinical microbiology reviews2002

Clinical and taxonomic status of pathogenic nonpigmented or late-pigmenting rapidly growing mycobacteria.

Barbara A Brown-Elliott, Richard J Wallace

Abstract readReview
In one paragraph

Review in Clinical microbiology reviews, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 325 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
325citing papers in PubMed, 4 pooled it
–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

325 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. A systematic review of tetracyclines for nontuberculous mycobacteria: focus on rapidly growing mycobacteria.European respiratory review : an official journal of the European Respiratory Society · 2025
    Pooled it
  2. Pooled it
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  6. Pathogens (Basel, Switzerland) · 2026
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  9. Successful treatment of pneumonia due toNew microbes and new infections · 2026
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  10. Canada communicable disease report = Releve des maladies transmissibles au Canada · 2026
    Article
  11. Article
  12. Review
  13. Description and complete genome sequence ofFrontiers in microbiology · 2026
    Article
  14. Pediatric Submandibular Lymphadenitis Caused byInfection and drug resistance · 2026
    Article
  15. A case of multiple abscesses caused byJournal of surgical case reports · 2025
    Article
  16. Review
  17. Genomic-enabled classification of threeJournal of clinical microbiology · 2025
    Article
  18. Article
  19. Article
  20. Article

265 more citing papers are in PubMed but not listed here.

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

2 authors.

Barbara A Brown-ElliottUniversity of Texas Health Center, Department of Microbiology, Tyler, Texas 75708, USA. barbara.elliott@uthct.edu
Richard J Wallace

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The history, taxonomy, geographic distribution, clinical disease, and therapy of the pathogenic nonpigmented or late-pigmenting rapidly growing mycobacteria (RGM) are reviewed. Community-acquired disease and health care-associated disease are highlighted for each species. The latter grouping includes health care-associated outbreaks and pseudo-outbreaks as well as sporadic disease cases. Treatment recommendations for each species and type of disease are also described. Special emphasis is on the Mycobacterium fortuitum group, including M. fortuitum, M. peregrinum, and the unnamed third biovariant complex with its recent taxonomic changes and newly recognized species (including M. septicum, M. mageritense, and proposed species M. houstonense and M. bonickei). The clinical and taxonomic status of M. chelonae, M. abscessus, and M. mucogenicum is also detailed, along with that of the closely related new species, M. immunogenum. Additionally, newly recognized species, M. wolinskyi and M. goodii, as well as M. smegmatis sensu stricto, are included in a discussion of the M. smegmatis group. Laboratory diagnosis of RGM using phenotypic methods such as biochemical testing and high-performance liquid chromatography and molecular methods of diagnosis are also discussed. The latter includes PCR-restriction fragment length polymorphism analysis, hybridization, ribotyping, and sequence analysis. Susceptibility testing and antibiotic susceptibility patterns of the RGM are also annotated, along with the current recommendations from the National Committee for Clinical Laboratory Standards (NCCLS) for mycobacterial susceptibility testing.

Indexed as

Anti-Bacterial AgentsCatheterizationCommunity-Acquired InfectionsHumansMicrobial Sensitivity TestsMycobacterium chelonaeMycobacterium fortuitumMycobacterium Infections, NontuberculousMycobacterium smegmatisOccupational DiseasesSkin Diseases, InfectiousWound InfectionAnti-Bacterial Agents

Identifiers

PMID12364376
PMCPMC126856

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.