TY - JOUR
T1 - Saliva Real-Time Polymerase Chain Reaction for Targeted Screening of Congenital Cytomegalovirus Infection
AU - Eventov-Friedman, Smadar
AU - Manor, Hili
AU - Bar-Oz, Benjamin
AU - Averbuch, Diana
AU - Caplan, Orit
AU - Lifshitz, Aliza
AU - Bdolah-Abram, Tali
AU - Wolf, Dana G.
N1 - Publisher Copyright: © 2019 The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: [email protected].
PY - 2019/10/22
Y1 - 2019/10/22
N2 - Background: Saliva real-Time polymerase chain reaction (PCR) was shown to be sensitive and specific for the detection of congenital cytomegalovirus (cCMV) in universal screening studies. In the current study, we assessed the performance of saliva real-Time PCR in newborns undergoing targeted cCMV screening. Methods: Saliva real-Time PCR results were prospectively correlated with reference-standard urine detection in newborns undergoing targeted cCMV screening over a 3-year period, in successive validation (concurrent testing of all saliva and urine specimens) and routine-screening (confirmatory urine testing of positive saliva results) implementation phases. Results: The sensitivity, specificity, and positive and negative predictive values of saliva real-Time PCR were 98.3% (95% confidence interval, 90.8%-99.9%), 91.5% (89.3%-93.3%), 45.6% (36.7%-54.7%), and 99.9% (99.2%-99.9%), respectively, in 856 concurrently tested newborns. True-positive saliva real-Time PCR detection (defined in relation to urine detection) was associated with earlier saliva sampling (P =. 002) and a higher saliva viral load (P <. 001). We further identified a saliva viral load cutoff value that reliably distinguished between true-positive and false-positive saliva results. Conclusions: In newborns undergoing targeted screening for cCMV, saliva real-Time PCR is highly sensitive yet has a low positive predictive value, necessitating confirmatory testing. Early sampling and application of a validated viral load cutoff could improve the assay performance and support its large-scale implementation in this growing clinical setting.
AB - Background: Saliva real-Time polymerase chain reaction (PCR) was shown to be sensitive and specific for the detection of congenital cytomegalovirus (cCMV) in universal screening studies. In the current study, we assessed the performance of saliva real-Time PCR in newborns undergoing targeted cCMV screening. Methods: Saliva real-Time PCR results were prospectively correlated with reference-standard urine detection in newborns undergoing targeted cCMV screening over a 3-year period, in successive validation (concurrent testing of all saliva and urine specimens) and routine-screening (confirmatory urine testing of positive saliva results) implementation phases. Results: The sensitivity, specificity, and positive and negative predictive values of saliva real-Time PCR were 98.3% (95% confidence interval, 90.8%-99.9%), 91.5% (89.3%-93.3%), 45.6% (36.7%-54.7%), and 99.9% (99.2%-99.9%), respectively, in 856 concurrently tested newborns. True-positive saliva real-Time PCR detection (defined in relation to urine detection) was associated with earlier saliva sampling (P =. 002) and a higher saliva viral load (P <. 001). We further identified a saliva viral load cutoff value that reliably distinguished between true-positive and false-positive saliva results. Conclusions: In newborns undergoing targeted screening for cCMV, saliva real-Time PCR is highly sensitive yet has a low positive predictive value, necessitating confirmatory testing. Early sampling and application of a validated viral load cutoff could improve the assay performance and support its large-scale implementation in this growing clinical setting.
KW - Congenital
KW - Cytomegalovirus
KW - Saliva
KW - Targeted screening
UR - http://www.scopus.com/inward/record.url?scp=85073662677&partnerID=8YFLogxK
U2 - 10.1093/infdis/jiz373
DO - 10.1093/infdis/jiz373
M3 - مقالة
C2 - 31310307
SN - 0022-1899
VL - 220
SP - 1790
EP - 1796
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 11
ER -