Author:
Roberts Tamalee,Chandna Arjun,Watthanaworawit Wanitda,Thaiprakong Areerat,Soeng Sona,Simmalavong Manivone,Phoumin Phonelavanh,Saengchun Weerawut,Khatta Nongyao,Hinfonthong Pattaraporn,Kaewpundoem Napaporn,Lee Sue J.,Perrone Carlo,Amos Ben,Turner Paul,Ashley Elizabeth A.,Ling Clare L.
Abstract
Abstract
Background
Blood cultures remain the gold standard investigation for the diagnosis of bloodstream infections. In many locations, quality-assured processing of positive blood cultures is not possible. One solution is to incubate blood cultures locally, and then transport bottles that flag positive to a central reference laboratory for organism identification and antimicrobial susceptibility testing. However, the impact of delay between the bottle flagging positive and subsequent sub-culture on the viability of the isolate has received little attention.
Methods
This study evaluated the impact of delays to sub-culture (22 h to seven days) in three different temperature conditions (2–8 °C, 22–27 °C and 35 ± 2 °C) for bottles that had flagged positive in automated detection systems using a mixture of spiked and routine clinical specimens. Ninety spiked samples for five common bacterial causes of sepsis (Escherichia coli, Haemophilus influenzae, Staphylococcus aureus, Streptococcus agalactiae and Streptococcus pneumoniae) and 125 consecutive positive clinical blood cultures were evaluated at four laboratories located in Cambodia, Lao PDR and Thailand. In addition, the utility of transport swabs for preserving organism viability was investigated.
Results
All organisms were recoverable from all sub-cultures in all temperature conditions with the exception of S. pneumoniae, which was less likely to be recoverable after longer delays (> 46–50 h), when stored in hotter temperatures (35 °C), and from BacT/ALERT when compared with BACTEC blood culture bottles. Storage of positive blood culture bottles in cooler temperatures (22–27 °C or below) and the use of Amies bacterial transport swabs helped preserve viability of S. pneumoniae.
Conclusions
These results have practical implications for the optimal workflow for blood culture bottles that have flagged positive in automated detection systems located remotely from a central processing laboratory, particularly in tropical resource-constrained contexts.
Publisher
Springer Science and Business Media LLC
Reference16 articles.
1. Report of the Review of NHS Pathology Services in England Chaired by Lord Carter of Coles. https://www.networks.nhs.uk/nhs-networks/peninsula-pathology-network/documents/CarterReviewPathologyReport.pdf. Accessed 16 Feb 2021.
2. Rönnberg C, Mildh M, Ullberg M, Özenci V. Transport time for blood culture bottles: underlying factors and its consequences. Diagn Microbiol Infect Dis. 2013;76(3):286–90.
3. Sautter RL, Bills AR, Lang DL, Ruschell G, Heiter BJ, Bourbeau PP. Effects of Delayed-entry conditions on the recovery and detection of microorganisms from BacT/ALERT and BACTEC blood culture bottles. J Clin Microbiol. 2006;44(4):1245.
4. Ling CL, Roberts T, Soeng S, Cusack TP, Dance DAB, Lee SJ, et al. Impact of delays to incubation and storage temperature on blood culture results: a multi-centre study. BMC Infect Dis. 2021;21(1):173.
5. Christner M, Rohde H, Wolters M, Sobottka I, Wegscheider K, Aepfelbacher M. Rapid identification of bacteria from positive blood culture bottles by use of matrix-assisted laser desorption-ionization time of flight mass spectrometry fingerprinting. J Clin Microbiol. 2010;48(5):1584–91.
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