학술논문

Bloodstream infections at a tertiary level paediatric hospital in South Africa.
Document Type
Journal Article
Source
BMC Infectious Diseases. 12/6/2017, Vol. 17, p1-9. 9p. 1 Diagram, 6 Charts.
Subject
*BLOODBORNE infections
*PEDIATRICS
*EPIDEMIOLOGY
*ANTIBIOTICS
*KLEBSIELLA pneumoniae
*ANEMIA diagnosis
*BACTEREMIA diagnosis
*DNA metabolism
*ANEMIA
*BACTEREMIA
*CHILDREN'S hospitals
*DNA
*GRAM-negative bacteria
*GRAM-positive bacteria
*INTENSIVE care units
*LEANNESS
*MULTIVARIATE analysis
*POLYMERASE chain reaction
*SPECIALTY hospitals
*COMMUNITY-acquired infections
*RELATIVE medical risk
*RETROSPECTIVE studies
*DISEASE complications
*DIAGNOSIS
Language
ISSN
1471-2334
Abstract
Background: Bloodstream infection (BSI) in children causes significant morbidity and mortality. There are few studies describing the epidemiology of BSI in South African children.Methods: A retrospective descriptive cohort study was conducted at a paediatric referral hospital in Cape Town, South Africa. The National Health Laboratory Service (NHLS) microbiology database was accessed to identify positive blood culture specimens during the period 2011-2012. Demographic and clinical details, antimicrobial management and patient outcome information were extracted from medical and laboratory records. Antibiotic susceptibility results of identified organisms were obtained from the NHLS database.Results: Of the 693 unique bacterial and fungal BSI episodes identified during the study period, 248 (35.8%) were community-acquired (CA), 371 (53.5%) hospital-acquired (HA) and 74 (10.7%) healthcare-associated (HCA). The overall risk was 6.7 BSI episodes per 1000 admissions. Escherichia coli, Staphylococcus aureus and Streptococcus pneumoniae were the most frequent causes of CA-BSI and Klebsiella pneumoniae, Acinetobacter baumanii and S.aureus were most commonly isolated in HA-BSI. On multivariable analysis, severe underweight, severe anaemia at the time of BSI, admission in the ICU at the time of BSI, and requiring ICU admission after BSI was diagnosed were significantly associated with 14-day mortality.Conclusion: This study adds to the limited literature describing BSI in children in Africa. Further studies are required to understand the impact that BSI has on the paediatric population in sub-Saharan Africa. [ABSTRACT FROM AUTHOR]