Utility of 16S rRNA PCR performed on clinical specimens in patient management

Background: Broad-range 16S rRNA PCR can be used for the detection and identification of bacteria from clinical specimens in patients for whom there is a high suspicion of infection and cultures are negative. The aims of this study were (1) to compare 16S rRNA PCR results with microbiological cultur...

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Main Authors: A. Akram, M. Maley, I. Gosbell, T. Nguyen, R. Chavada
Format: Article
Language:English
Published: Elsevier 2017-04-01
Series:International Journal of Infectious Diseases
Subjects:
16S
Online Access:http://www.sciencedirect.com/science/article/pii/S1201971217300528
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spelling doaj-3855a3b627dd4980a708b7a10359739e2020-11-24T21:53:33ZengElsevierInternational Journal of Infectious Diseases1201-97121878-35112017-04-0157C14414910.1016/j.ijid.2017.02.006Utility of 16S rRNA PCR performed on clinical specimens in patient managementA. Akram0M. Maley1I. Gosbell2T. Nguyen3R. Chavada4Department of Microbiology and Infectious Diseases, Sydney South West Pathology Services, Liverpool Hospital, Liverpool, NSW, AustraliaDepartment of Microbiology and Infectious Diseases, Sydney South West Pathology Services, Liverpool Hospital, Liverpool, NSW, AustraliaDepartment of Microbiology and Infectious Diseases, Sydney South West Pathology Services, Liverpool Hospital, Liverpool, NSW, AustraliaInstitute of Clinical Pathology and Medical Research, Westmead Hospital, Westmead, NSW, AustraliaDepartment of Microbiology and Infectious Diseases, Pathology North, Gosford/Wyong Hospitals, Gosford, NSW, AustraliaBackground: Broad-range 16S rRNA PCR can be used for the detection and identification of bacteria from clinical specimens in patients for whom there is a high suspicion of infection and cultures are negative. The aims of this study were (1) to compare 16S rRNA PCR results with microbiological culture results, (2) to assess the utility of 16S rRNA PCR with regard to antimicrobial therapy, and (3) to compare the yield of 16S rRNA PCR for different types of clinical specimen and to perform a cost analysis of the test. Methods: A retrospective study was performed on different clinical specimens which had 16S performed over 3 years (2012–2015). Standard microbiological cultures were performed on appropriate media, as per the laboratory protocol. Patient clinical and microbiological data were obtained from the electronic medical records and laboratory information system, respectively. 16S rRNA PCR was performed in a reference laboratory using a validated method for amplification and sequencing. The outcomes assessed were the performance of 16S rRNA PCR, change of antimicrobials (rationalization, cessation, or addition), and duration of therapy. Concordance of 16S rRNA PCR with bacterial cultures was also determined for tissue specimens. Results: Thirty-two patients were included in the study, for whom an equal number of specimens (n = 32) were sent for 16S rRNA PCR. 16S rRNA PCR could identify an organism in 10 of 32 cases (31.2%), of which seven were culture-positive and three were culture-negative. The sensitivity was 58% (confidence interval (CI) 28.59–83.5%) and specificity was 85% (CI 61.13–96%), with a positive predictive value of 70% (CI 35.3–91.9%) and negative predictive value of 77.2% (CI 54.17–91.3%). Antimicrobial therapy was rationalized after 16S rRNA PCR results in five patients (15.6%) and was ceased in four based on negative results (12.5%). Overall the 16S rRNA PCR result had an impact on antimicrobial therapy in 28% of patients (9/32). The highest concordance of 16S rRNA PCR with bacterial culture was found for heart valve tissue (80%), followed by joint fluid/tissue (50%). Conclusions: Despite the low diagnostic yield, results of 16S rRNA PCR can still have a significant impact on patient management due to rationalization or cessation of the antimicrobial therapy. The yield of 16S rRNA PCR was highest for heart valves.http://www.sciencedirect.com/science/article/pii/S120197121730052816S16S rRNAUtilityBacterial infectionsCost analysis
collection DOAJ
language English
format Article
sources DOAJ
author A. Akram
M. Maley
I. Gosbell
T. Nguyen
R. Chavada
spellingShingle A. Akram
M. Maley
I. Gosbell
T. Nguyen
R. Chavada
Utility of 16S rRNA PCR performed on clinical specimens in patient management
International Journal of Infectious Diseases
16S
16S rRNA
Utility
Bacterial infections
Cost analysis
author_facet A. Akram
M. Maley
I. Gosbell
T. Nguyen
R. Chavada
author_sort A. Akram
title Utility of 16S rRNA PCR performed on clinical specimens in patient management
title_short Utility of 16S rRNA PCR performed on clinical specimens in patient management
title_full Utility of 16S rRNA PCR performed on clinical specimens in patient management
title_fullStr Utility of 16S rRNA PCR performed on clinical specimens in patient management
title_full_unstemmed Utility of 16S rRNA PCR performed on clinical specimens in patient management
title_sort utility of 16s rrna pcr performed on clinical specimens in patient management
publisher Elsevier
series International Journal of Infectious Diseases
issn 1201-9712
1878-3511
publishDate 2017-04-01
description Background: Broad-range 16S rRNA PCR can be used for the detection and identification of bacteria from clinical specimens in patients for whom there is a high suspicion of infection and cultures are negative. The aims of this study were (1) to compare 16S rRNA PCR results with microbiological culture results, (2) to assess the utility of 16S rRNA PCR with regard to antimicrobial therapy, and (3) to compare the yield of 16S rRNA PCR for different types of clinical specimen and to perform a cost analysis of the test. Methods: A retrospective study was performed on different clinical specimens which had 16S performed over 3 years (2012–2015). Standard microbiological cultures were performed on appropriate media, as per the laboratory protocol. Patient clinical and microbiological data were obtained from the electronic medical records and laboratory information system, respectively. 16S rRNA PCR was performed in a reference laboratory using a validated method for amplification and sequencing. The outcomes assessed were the performance of 16S rRNA PCR, change of antimicrobials (rationalization, cessation, or addition), and duration of therapy. Concordance of 16S rRNA PCR with bacterial cultures was also determined for tissue specimens. Results: Thirty-two patients were included in the study, for whom an equal number of specimens (n = 32) were sent for 16S rRNA PCR. 16S rRNA PCR could identify an organism in 10 of 32 cases (31.2%), of which seven were culture-positive and three were culture-negative. The sensitivity was 58% (confidence interval (CI) 28.59–83.5%) and specificity was 85% (CI 61.13–96%), with a positive predictive value of 70% (CI 35.3–91.9%) and negative predictive value of 77.2% (CI 54.17–91.3%). Antimicrobial therapy was rationalized after 16S rRNA PCR results in five patients (15.6%) and was ceased in four based on negative results (12.5%). Overall the 16S rRNA PCR result had an impact on antimicrobial therapy in 28% of patients (9/32). The highest concordance of 16S rRNA PCR with bacterial culture was found for heart valve tissue (80%), followed by joint fluid/tissue (50%). Conclusions: Despite the low diagnostic yield, results of 16S rRNA PCR can still have a significant impact on patient management due to rationalization or cessation of the antimicrobial therapy. The yield of 16S rRNA PCR was highest for heart valves.
topic 16S
16S rRNA
Utility
Bacterial infections
Cost analysis
url http://www.sciencedirect.com/science/article/pii/S1201971217300528
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