A retrospective evaluation of a multiplex polymerase chain reaction test directly applied to blood for the management of sepsis in the critically ill.

ICU PCR blood culture bloodstream infections critically illness polymerase chain reaction sepsis

Journal

The Southern African journal of critical care : the official journal of the Critical Care Society
ISSN: 2078-676X
Titre abrégé: South Afr J Crit Care
Pays: South Africa
ID NLM: 8801525

Informations de publication

Date de publication:
2021
Historique:
accepted: 04 08 2021
entrez: 6 5 2022
pubmed: 7 5 2022
medline: 7 5 2022
Statut: epublish

Résumé

Blood culture (BC) is the established gold standard for microbiological diagnosis of bloodstream infection (BSI); however, its sensitivity is poor. The primary objective was to determine the sensitivity and specificity of the Magicplex Sepsis Real-time Test, a multiplex polymerase chain reaction test (mPCR), and BC to detect BSIs. Secondary outcomes included determining the prevalence of BSIs. A retrospective review of a technical evaluation of the mPCR. Patients requiring BC had a blood sample collected for mPCR. The respective sensitivity and specificity of mPCR for the detection of BSI were 50% (n=7/14) and 58% (n=18/31), while the sensitivity and specificity using BC were 36% (n=5/14) and 68% (n=21/31), respectively. The addition of mPCR to BC increased BSI detection during sepsis from 36% to 64%. The use of mPCR directly applied to blood may increase the detection of micro-organisms associated with BSIs in critically ill patients requiring BC investigation. Our data add to a growing body of evidence indicating that mPCR applied directly to blood prior to incubation increases the detection of pathogenic bacteria among hospitalised patients for whom blood cultures are performed for suspected infection. Our study was performed in a low-to-middle income country with a higher sepsis prevalence, a greater burden of multidrug-resistant organisms and clinically defined sepsis. This strengthens the robustness and generalisability of this body of evidence.

Sections du résumé

Background UNASSIGNED
Blood culture (BC) is the established gold standard for microbiological diagnosis of bloodstream infection (BSI); however, its sensitivity is poor.
Objectives UNASSIGNED
The primary objective was to determine the sensitivity and specificity of the Magicplex Sepsis Real-time Test, a multiplex polymerase chain reaction test (mPCR), and BC to detect BSIs. Secondary outcomes included determining the prevalence of BSIs.
Methods UNASSIGNED
A retrospective review of a technical evaluation of the mPCR. Patients requiring BC had a blood sample collected for mPCR.
Results UNASSIGNED
The respective sensitivity and specificity of mPCR for the detection of BSI were 50% (n=7/14) and 58% (n=18/31), while the sensitivity and specificity using BC were 36% (n=5/14) and 68% (n=21/31), respectively. The addition of mPCR to BC increased BSI detection during sepsis from 36% to 64%.
Conclusion UNASSIGNED
The use of mPCR directly applied to blood may increase the detection of micro-organisms associated with BSIs in critically ill patients requiring BC investigation.
Contributions of the study UNASSIGNED
Our data add to a growing body of evidence indicating that mPCR applied directly to blood prior to incubation increases the detection of pathogenic bacteria among hospitalised patients for whom blood cultures are performed for suspected infection. Our study was performed in a low-to-middle income country with a higher sepsis prevalence, a greater burden of multidrug-resistant organisms and clinically defined sepsis. This strengthens the robustness and generalisability of this body of evidence.

Identifiants

pubmed: 35517850
doi: 10.7196/SAJCC.2021.v37i3.495
pmc: PMC9053419
doi:

Types de publication

Journal Article

Langues

eng

Déclaration de conflit d'intérêts

Conflicts of interest: None.

Références

Lancet Infect Dis. 2009 Sep;9(9):577-82
pubmed: 19695494
JAMA. 2016 Feb 23;315(8):801-10
pubmed: 26903338
Ann Transl Med. 2020 May;8(9):610
pubmed: 32566636
Intensive Care Med. 2020 Feb;46(2):266-284
pubmed: 32047941
PLoS One. 2016 Dec 20;11(12):e0167883
pubmed: 27997618
J Med Microbiol. 2013 Nov;62(Pt 11):1673-1679
pubmed: 23924662
Crit Rev Microbiol. 2018 May;44(3):351-370
pubmed: 29185372
Crit Care. 2009;13(4):217
pubmed: 19664174
Crit Care Med. 2017 Mar;45(3):486-552
pubmed: 28098591
BMC Infect Dis. 2015 Apr 28;15:199
pubmed: 25928122
Clin Microbiol Infect. 2015 Apr;21(4):313-22
pubmed: 25753137
Health Technol Assess. 2015 May;19(35):1-142
pubmed: 25961752
J Clin Microbiol. 2003 Jun;41(6):2275-8
pubmed: 12791835
Front Cell Infect Microbiol. 2019 Mar 12;9:56
pubmed: 30931259
PLoS One. 2013 May 29;8(5):e62323
pubmed: 23734173

Auteurs

S Omar (S)

Critical Care, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

S Murphy (S)

Critical Care, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

R Gheevarghese (R)

Critical Care, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

N Poppleton (N)

Critical Care, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Classifications MeSH