Detailed Information on Publication Record
2016
Necrotizing pneumonia due to clonally diverse Staphylococcus aureus strains producing Panton-Valentine leukocidin: the Czech experience
RÁJOVÁ, Jana, Roman PANTŮČEK, Petr PETRÁŠ, Ivana VARBANOVOVÁ, Ivana MAŠLAŇOVÁ et. al.Basic information
Original name
Necrotizing pneumonia due to clonally diverse Staphylococcus aureus strains producing Panton-Valentine leukocidin: the Czech experience
Authors
RÁJOVÁ, Jana (203 Czech Republic, belonging to the institution), Roman PANTŮČEK (203 Czech Republic, guarantor, belonging to the institution), Petr PETRÁŠ (203 Czech Republic), Ivana VARBANOVOVÁ (203 Czech Republic), Ivana MAŠLAŇOVÁ (203 Czech Republic, belonging to the institution) and Jiří BENEŠ (203 Czech Republic)
Edition
Epidemiology & Infection, Cambridge University Press, 2016, 0950-2688
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10600 1.6 Biological sciences
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.075
RIV identification code
RIV/00216224:14310/16:00087773
Organization unit
Faculty of Science
UT WoS
000368636200006
Keywords in English
Community-acquired pneumonia; necrotizing pneumonia; Panton–Valentine leukocidin; septic shock; Staphylococcus aureus
Tags
International impact, Reviewed
Změněno: 26/10/2020 10:44, prof. RNDr. Roman Pantůček, Ph.D.
Abstract
V originále
A prospective study (2007–2013) was undertaken to investigate clinical features and prognostic factors of necrotizing pneumonia caused by Staphylococcus aureus producing Panton–Valentine leukocidin (PVL) in the Czech Republic. Twelve cases of necrotizing pneumonia were detected in 12 patients (median age 25 years) without severe underlying disease. Eight cases occurred in December and January and the accumulation of cases in the winter months preceding the influenza season was statistically significant (P < 0·001). The course of pneumonia was very rapid, leading to early sepsis and/or septic shock in all but one patient. Seven patients died and mortality was fourfold higher in those patients presenting with primary pneumonia than with pneumonia complicating other staphylococcal/pyogenic infection elsewhere in the body. The S. aureus isolates displayed considerable genetic variability and were assigned to five lineages CC8 (n = 3), CC15 (n = 2), CC30 (n = 2), CC80 (n = 1), and CC121 (n = 3) and one was a singleton of ST154 (n = 1), all were reported to be associated with community-acquired infection. Four strains were methicillin resistant. The high case-fatality rate can only be reduced by improving the speed of diagnosis and a rapid test to detect S. aureus in the airways is needed.
Links
GP13-05069P, research and development project |
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NT12395, research and development project |
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