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Wild-type MIC distributions of four fluoroquinolones active against Mycobacterium tuberculosis in relation to current critical concentrations and available pharmacokinetic and pharmacodynamic data

Ängeby, Kristian A. (author)
Karolinska Institutet,Karolinska University Hospital
Jureen, P. (author)
Swedish Institute for Infectious Disease Control
Giske, C. G. (author)
Karolinska Institutet,Karolinska University Hospital
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Chryssanthou, E. (author)
Karolinska Institutet,Karolinska University Hospital
Sturegård, Erik (author)
Lund University,Lunds universitet,Klinisk mikrobiologi, Malmö,Forskargrupper vid Lunds universitet,Clinical Microbiology, Malmö,Lund University Research Groups,Malmo University Hospital,Swedish Institute for Infectious Disease Control
Nordvall, Maria (author)
Östergötlands Läns Landsting,Linköpings universitet,Pediatrik,Hälsouniversitetet,Barn- och ungdomskliniken i Linköping
Johansson, A. G. (author)
Linköpings universitet,Institutionen för klinisk och experimentell medicin,Hälsouniversitetet
Werngren, J. (author)
Swedish Institute for Infectious Disease Control
Kahlmeter, Gunnar (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,klinisk bakteriologi,Växjö Hospital
Hoffner, S. E. (author)
Schön, T. (author)
Kalmar County Hospital
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 (creator_code:org_t)
2010-03-23
2010
English.
In: Journal of Antimicrobial Chemotherapy. - : Oxford University Press (OUP). - 0305-7453 .- 1460-2091. ; 65:5, s. 946-952
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • OBJECTIVES: To describe wild-type distributions of the MIC of fluoroquinolones for Mycobacterium tuberculosis in relation to current critical concentrations used for drug susceptibility testing and pharmacokinetic/pharmacodynamic (PK/PD) data. METHODS: A 96-stick replicator on Middlebrook 7H10 medium was used to define the MICs of ciprofloxacin, ofloxacin, moxifloxacin and levofloxacin for 90 consecutive clinical strains and 24 drug-resistant strains. The MICs were compared with routine BACTEC 460 susceptibility results and with MIC determinations in the BACTEC MGIT 960 system in a subset of strains using ofloxacin as a class representative. PK/PD data for each drug were reviewed in relation to the wild-type MIC distribution. RESULTS: The wild-type MICs of ciprofloxacin, ofloxacin, moxifloxacin and levofloxacin were distributed from 0.125 to 1, 0.25 to 1, 0.032 to 0.5 and 0.125 to 0.5 mg/L, respectively. The MIC data correlated well with the BACTEC 960 MGIT and BACTEC 460 results. PD indices were the most favourable for levofloxacin, followed by moxifloxacin, ofloxacin and ciprofloxacin. CONCLUSIONS: We propose S (susceptible)

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Keyword

ciprofloxacin
ofloxacin
moxifloxacin
levofloxacin
susceptibility testing
MEDICINE
MEDICIN
levofloxacin
moxifloxacin
ciprofloxacin
ofloxacin
susceptibility
testing
TECHNOLOGY

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art (subject category)

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