Evidence map›Paper›PMID 28882177›Full record

ArticleBMC research notes2017

AmpC and extended spectrum beta-lactamases production among urinary isolates from a tertiary care hospital in Lalitpur, Nepal.

Suman Rai, Narayan Dutt Pant, Raju Bhandari, Anil Giri, Roshan Parajuli, Manoj Aryal, Jyoti Amatya, Vijay Kumar Sharma

Open access · goldAbstract read
In one paragraph

Article in BMC research notes, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Detection of plasmid-mediated AmpC β-lactamases inIranian journal of microbiology · 2023
    Article
  4. Review
  5. Article
  6. Extended-Spectrum β-Lactamase-ProducingInfectious diseases · 2020
    Article
  7. 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 at 3 institutions in 2 countries.

Suman RaiDepartment of Microbiology, Tri-Chandra Multiple Campus, Kathmandu, Nepal.
Narayan Dutt PantDepartment of Microbiology, Grande International Hospital, Kathmandu, Nepal. ndpant1987@gmail.com.
Raju BhandariDepartment of Microbiology, Goldengate International College, Kathmandu, Nepal.
Anil GiriDepartment of Microbiology, Goldengate International College, Kathmandu, Nepal.
Roshan ParajuliDepartment of Microbiology, St. Xaviers College, Kathmandu, Nepal.
Manoj AryalDepartment of Microbiology, Tri-Chandra Multiple Campus, Kathmandu, Nepal.
Jyoti AmatyaDepartment of Microbiology, Tri-Chandra Multiple Campus, Kathmandu, Nepal.
Vijay Kumar SharmaInstitute of Medicine, Tribhuvan University, Kathmandu, Nepal.
Tribhuvan University · NPGrande International Hospital · NPSt Xavier’s College · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProduction of AmpC and extended spectrum beta-lactamases among urinary isolates has created a serious problem to the successful management of the urinary tract infection. The main purpose of this study was to determine the rates of the extended spectrum beta-lactamase (ESBL) production and AmpC beta-lactamase (ABL) production among urinary isolates.

resultsAmong total 564 urinary isolates, 514 (91.1%) were gram negative bacilli and 50 (8.9%) were gram positive cocci. E. coli (76.1%) was the most common bacteria isolated. Staphylococcus aureus (6.7%) was the predominant gram positive bacteria isolated. 35 (6.8%) of the 514 gram negative bacilli were ESBL producers. Similarly, 14 (2.7%) of the gram negative bacilli were ABL producers. Only one isolate was ESBL and ABL co-producer. Highest rate of susceptibility of gram negative bacteria was seen toward amikacin (97.3%) followed by imipenem (94.4%). Similarly, highest rate of susceptibility among gram positive cocci was seen toward vancomycin (100%) followed by amikacin (93.5%).

conclusionsLow rates of AmpC and extended spectrum beta-lactamases production in comparison to other previous studies were reported. On the basis of the antimicrobial susceptibility patterns of the bacteria we reported in our study, amikacin, imipenem and nitrofurantoin can be used for the preliminary treatment of urinary tract infections caused by gram negative bacteria and vancomycin and amikacin for treatment of urinary tract infections caused by gram positive bacteria.

Indexed as

Drug Resistance, BacterialAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasesEscherichia coliGram-Negative BacteriaGram-Positive BacteriaHumansMicrobial Sensitivity TestsNepalStaphylococcus aureusTertiary Care CentersUrinary Tract InfectionsAmpC beta-lactamasesAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasesABLCo-productionESBLNepalUrinary tract infection

Identifiers

PMID28882177
PMCPMC5590110
OpenAlexW2752629541

What OpenQuestion holds

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LicenceCC BY
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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.