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Distinguishing Severe Acute Respiratory Syndrome Coronavirus 2 Persistence and Reinfection: A Retrospective Cohort Study.
Turbett, Sarah E; Tomkins-Tinch, Christopher H; Anahtar, Melis N; Dugdale, Caitlin M; Hyle, Emily P; Shenoy, Erica S; Shaw, Bennett; Egbuonu, Kenechukwu; Bowman, Kathryn A; Zachary, Kimon C; Adams, Gordon C; Hooper, David C; Ryan, Edward T; LaRocque, Regina C; Bassett, Ingrid V; Triant, Virginia A; Siddle, Katherine J; Rosenberg, Eric; Sabeti, Pardis C; Schaffner, Stephen F; MacInnis, Bronwyn L; Lemieux, Jacob E; Charles, Richelle C.
Afiliação
  • Turbett SE; Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Tomkins-Tinch CH; Harvard Medical School, Boston, Massachusetts, USA.
  • Anahtar MN; Department of Pathology, Massachusetts General Hospital (MGH), Boston, Massachusetts, USA.
  • Dugdale CM; Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard, Cambridge, Massachusetts, USA.
  • Hyle EP; Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts, USA.
  • Shenoy ES; Department of Pathology, Massachusetts General Hospital (MGH), Boston, Massachusetts, USA.
  • Shaw B; Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard, Cambridge, Massachusetts, USA.
  • Egbuonu K; Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Bowman KA; Harvard Medical School, Boston, Massachusetts, USA.
  • Zachary KC; Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Adams GC; Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Hooper DC; Harvard Medical School, Boston, Massachusetts, USA.
  • Ryan ET; Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • LaRocque RC; Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Bassett IV; Harvard Medical School, Boston, Massachusetts, USA.
  • Triant VA; Infection Control Unit, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Siddle KJ; Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Rosenberg E; Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard, Cambridge, Massachusetts, USA.
  • Sabeti PC; David Geffen School of Medicine at the University of California Los Angeles, Los Angeles, California, USA.
  • Schaffner SF; Massachusetts Institute of Technology, Boston, Massachusetts, USA.
  • MacInnis BL; Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Lemieux JE; Harvard Medical School, Boston, Massachusetts, USA.
  • Charles RC; Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts, USA.
Clin Infect Dis ; 76(5): 850-860, 2023 03 04.
Article em En | MEDLINE | ID: mdl-36268576
BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) reinfection is poorly understood, partly because few studies have systematically applied genomic analysis to distinguish reinfection from persistent RNA detection related to initial infection. We aimed to evaluate the characteristics of SARS-CoV-2 reinfection and persistent RNA detection using independent genomic, clinical, and laboratory assessments. METHODS: All individuals at a large academic medical center who underwent a SARS-CoV-2 nucleic acid amplification test (NAAT) ≥45 days after an initial positive test, with both tests between 14 March and 30 December 2020, were analyzed for potential reinfection. Inclusion criteria required having ≥2 positive NAATs collected ≥45 days apart with a cycle threshold (Ct) value <35 at repeat testing. For each included subject, likelihood of reinfection was assessed by viral genomic analysis of all available specimens with a Ct value <35, structured Ct trajectory criteria, and case-by-case review by infectious diseases physicians. RESULTS: Among 1569 individuals with repeat SARS-CoV-2 testing ≥45 days after an initial positive NAAT, 65 (4%) met cohort inclusion criteria. Viral genomic analysis characterized mutations present and was successful for 14/65 (22%) subjects. Six subjects had genomically supported reinfection, and 8 subjects had genomically supported persistent RNA detection. Compared to viral genomic analysis, clinical and laboratory assessments correctly distinguished reinfection from persistent RNA detection in 12/14 (86%) subjects but missed 2/6 (33%) genomically supported reinfections. CONCLUSIONS: Despite good overall concordance with viral genomic analysis, clinical and Ct value-based assessments failed to identify 33% of genomically supported reinfections. Scaling-up genomic analysis for clinical use would improve detection of SARS-CoV-2 reinfections.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: COVID-19 Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: COVID-19 Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos