Florina Olivia Buzdug
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Florina Olivia Buzdug has a total of 16 co-authors. Here are the top co-authors by number of shared publications:
- Alexandra Manuela Buzle
Department of Medical Disciplines, Faculty of Medicine and Pharmacy, University of Oradea, 410073 Oradea, Romania
1 shared publication - Alina Stanca Osiceanu
Department of Medical Disciplines, Faculty of Medicine and Pharmacy, University of Oradea, 410073 Oradea, Romania
1 shared publication - Andrei Daescu
Doctoral School Department, “Victor Babes” University of Medicine and Pharmacy, 300041 Timisoara, Romania
1 shared publication - Andrei Nicolae Csep
Department of Psycho-Neurosciences and Recovery, Faculty of Medicine and Pharmacy, University of Oradea, 1 December Square 10, 410073 Oradea, Romania
1 shared publication - Claudia Elena Staniș
Faculty of Medicine and Pharmacy, University of Oradea, 410073 Oradea, Romania
1 shared publication - Corina-Maria Botici
Clinical Hospital of Infectious Diseases and Pneumophthisiology “Dr. Victor Babeș”, 300173 Timișoara, Romania
1 shared publication
Latest Publications
- Open Access
- 25 September 2026
- Published by MDPI AG in Diagnostics
- Vol. 16 (19) , 3125
Diagnostic Yield and Incremental Value of 16S rRNA Gene PCR and Sequencing on Excised Heart-Valve Tissue in Infective Endocarditis: A Systematic Review and Meta-Analysis
Background/Objectives: Broad-range bacterial 16S rRNA gene PCR followed by sequencing may improve the etiological diagnosis of infective endocarditis (IE), particularly when conventional cultures are negative. This systematic review and meta-analysis evaluated the overall molecular detection yield and incremental value of valve-tissue 16S molecular testing in surgically managed IE. Methods: PubMed/MEDLINE, Scopus, Web of Science Core Collection, and Europe PMC were searched for Open Access studies published from 2016 to 2026. Eligible studies evaluated broad-range bacterial 16S PCR with sequence-based identification on excised native or prosthetic heart-valve tissue. Random-effects generalized linear mixed models were used to pool overall diagnostic yield, strict blood-culture-negative IE (BCNE) yield, and strict incremental etiologic yield beyond conventional microbiology. Diagnostic accuracy was summarized descriptively when complete 2 × 2 data were available. Results: Eight studies comprising 925 patients, surgical cases, or IE episodes contributed to the primary analysis, with 704 study-reported molecular-positive results. The pooled diagnostic yield was 75.9% (95% CI, 68.7–82.0%), with substantial heterogeneity (I2 = 81.8%) and a 95% prediction interval of 49.2–91.2%. In strict BCNE, the pooled yield was 53.7% (95% CI, 41.2–65.8%). The strict incremental etiologic yield was 8.8% (95% CI, 6.1–12.5%). Sensitivity analyses yielded similar estimates. Conclusions: Valve-tissue 16S PCR/sequencing can provide valuable etiological information, particularly in BCNE. However, the substantial between-study heterogeneity and wide prediction interval indicate that its expected molecular detection yield varies considerably across clinical settings and is influenced by patient selection, local diagnostic algorithms, laboratory methods, and reference standards.
- 25 September 2026
- Published by MDPI AG in Diagnostics
- Vol. 16 (19) , 3125
Open AccessDiagnostic Yield and Incremental Value of 16S rRNA Gene PCR and Sequencing on Excised Heart-Valve Tissue in Infective Endocarditis: A Systematic Review and Meta-Analysis
Background/Objectives: Broad-range bacterial 16S rRNA gene PCR followed by sequencing may improve the etiological diagnosis of infective endocarditis (IE), particularly when conventional cultures are negative. This systematic review and meta-analysis evaluated the overall molecular detection yield and incremental value of valve-tissue 16S molecular testing in surgically managed IE. Methods: PubMed/MEDLINE, Scopus, Web of Science Core Collection, and Europe PMC were searched for Open Access studies published from 2016 to 2026. Eligible studies evaluated broad-range bacterial 16S PCR with sequence-based identification on excised native or prosthetic heart-valve tissue. Random-effects generalized linear mixed models were used to pool overall diagnostic yield, strict blood-culture-negative IE (BCNE) yield, and strict incremental etiologic yield beyond conventional microbiology. Diagnostic accuracy was summarized descriptively when complete 2 × 2 data were available. Results: Eight studies comprising 925 patients, surgical cases, or IE episodes contributed to the primary analysis, with 704 study-reported molecular-positive results. The pooled diagnostic yield was 75.9% (95% CI, 68.7–82.0%), with substantial heterogeneity (I2 = 81.8%) and a 95% prediction interval of 49.2–91.2%. In strict BCNE, the pooled yield was 53.7% (95% CI, 41.2–65.8%). The strict incremental etiologic yield was 8.8% (95% CI, 6.1–12.5%). Sensitivity analyses yielded similar estimates. Conclusions: Valve-tissue 16S PCR/sequencing can provide valuable etiological information, particularly in BCNE. However, the substantial between-study heterogeneity and wide prediction interval indicate that its expected molecular detection yield varies considerably across clinical settings and is influenced by patient selection, local diagnostic algorithms, laboratory methods, and reference standards.