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Saliva Real-Time Polymerase Chain Reaction for Targeted Screening of Congenital Cytomegalovirus Infection.
Eventov-Friedman, Smadar; Manor, Hili; Bar-Oz, Benjamin; Averbuch, Diana; Caplan, Orit; Lifshitz, Aliza; Bdolah-Abram, Tali; Wolf, Dana G.
Afiliação
  • Eventov-Friedman S; Department of Neonatology, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Manor H; Clinical Virology Unit, Department of Clinical Microbiology and Infectious Diseases, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Bar-Oz B; Department of Neonatology, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Averbuch D; Pediatric Infectious Diseases, Pediatric Division, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Caplan O; Clinical Virology Unit, Department of Clinical Microbiology and Infectious Diseases, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Lifshitz A; Clinical Virology Unit, Department of Clinical Microbiology and Infectious Diseases, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Bdolah-Abram T; Hebrew University Faculty of Medicine, Jerusalem, Israel.
  • Wolf DG; Clinical Virology Unit, Department of Clinical Microbiology and Infectious Diseases, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
J Infect Dis ; 220(11): 1790-1796, 2019 10 22.
Article em En | MEDLINE | ID: mdl-31310307
ABSTRACT

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saliva / Programas de Rastreamento / Infecções por Citomegalovirus / Citomegalovirus / Técnicas de Diagnóstico Molecular / Reação em Cadeia da Polimerase em Tempo Real Tipo de estudo: Diagnostic_studies / Evaluation_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Female / Humans / Male / Newborn Idioma: En Revista: J Infect Dis Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Israel

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saliva / Programas de Rastreamento / Infecções por Citomegalovirus / Citomegalovirus / Técnicas de Diagnóstico Molecular / Reação em Cadeia da Polimerase em Tempo Real Tipo de estudo: Diagnostic_studies / Evaluation_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Female / Humans / Male / Newborn Idioma: En Revista: J Infect Dis Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Israel