Tiffany Wu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Tiffany Wu has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Alex Rock
Massachusetts General Hospital
1 shared publication - Alyssa R. Letourneau
Massachusetts General Hospital
1 shared publication - Carissa Tedeschi
Massachusetts General Hospital
1 shared publication - Cecilia Li
Massachusetts General Hospital
1 shared publication - Eric Gillett
Department of Pharmacy, Brigham and Women's Hospital , Boston, Massachusetts
1 shared publication Erin K. McCreary
1 shared publication
Latest Publications
- Open Access
- 3 August 2026
- Published by Wiley in Transplant Infectious Disease
- p. e70262
Long‐Term Use of Rezafungin: A Case Report and Insights Into Real‐World Access
- 3 August 2026
- Published by Wiley in Transplant Infectious Disease
- p. e70262
Open AccessLong‐Term Use of Rezafungin: A Case Report and Insights Into Real‐World Access
- Open Access
- 15 June 2026
- Published by Cambridge University Press (CUP) in Antimicrobial Stewardship & Healthcare Epidemiology
- Vol. 6 (1)
Outcomes of early oral antibiotic transition for the treatment of uncomplicated enterococcal bacteremia
Objective: To compare clinical outcomes in adults with uncomplicated enterococcal bacteremia treated with intravenous (IV) therapy alone versus an early oral (PO) transition and evaluate treatment characteristics and safety outcomes. Design: Retrospective cohort study between January 1, 2021, and August 1, 2024. The primary outcome was clinical cure at 90 days after antibiotic completion. Secondary outcomes included treatment failure, infection-related readmission, hospital length of stay (HLOS), and 90-day mortality. Setting: Massachusetts General Hospital and Brigham and Women’s Hospital, two tertiary care centers in Boston, MA. Patients: Adult patients with at least one positive blood culture with Enterococcus spp. Patients were excluded if they had polymicrobial or persistent bacteremia, invasive infection, incomplete source control, died before completing therapy, or received fewer than 7 days of antibiotics. Results: 209 patients were included, of which 119 received IV therapy alone and 90 underwent early PO transition. Gastrointestinal (41.6%) and genitourinary (32.1%) sources were most common, and 86 patients (41.1%) had immunocompromising conditions. Clinical cure was similar between the IV and early PO transition groups (73.9% vs 82.2%; P = .156), with no significant differences in secondary and safety outcomes. HLOS was significantly shorter in the early PO transition group (9 days vs 20 days; P < .001). Conclusion: Early PO transition appears to be a safe and effective strategy for uncomplicated enterococcal bacteremia and was associated with reduced HLOS.
- 15 June 2026
- Published by Cambridge University Press (CUP) in Antimicrobial Stewardship & Healthcare Epidemiology
- Vol. 6 (1)
Open AccessOutcomes of early oral antibiotic transition for the treatment of uncomplicated enterococcal bacteremia
Objective: To compare clinical outcomes in adults with uncomplicated enterococcal bacteremia treated with intravenous (IV) therapy alone versus an early oral (PO) transition and evaluate treatment characteristics and safety outcomes. Design: Retrospective cohort study between January 1, 2021, and August 1, 2024. The primary outcome was clinical cure at 90 days after antibiotic completion. Secondary outcomes included treatment failure, infection-related readmission, hospital length of stay (HLOS), and 90-day mortality. Setting: Massachusetts General Hospital and Brigham and Women’s Hospital, two tertiary care centers in Boston, MA. Patients: Adult patients with at least one positive blood culture with Enterococcus spp. Patients were excluded if they had polymicrobial or persistent bacteremia, invasive infection, incomplete source control, died before completing therapy, or received fewer than 7 days of antibiotics. Results: 209 patients were included, of which 119 received IV therapy alone and 90 underwent early PO transition. Gastrointestinal (41.6%) and genitourinary (32.1%) sources were most common, and 86 patients (41.1%) had immunocompromising conditions. Clinical cure was similar between the IV and early PO transition groups (73.9% vs 82.2%; P = .156), with no significant differences in secondary and safety outcomes. HLOS was significantly shorter in the early PO transition group (9 days vs 20 days; P < .001). Conclusion: Early PO transition appears to be a safe and effective strategy for uncomplicated enterococcal bacteremia and was associated with reduced HLOS.
- Open Access
- 3 April 2026
- Published by Elsevier in CMI Communications
- Vol. 3 (2)
Oral fosfomycin tromethamine for UTI: Guidance for clinicians
- 3 April 2026
- Published by Elsevier in CMI Communications
- Vol. 3 (2)
Open AccessOral fosfomycin tromethamine for UTI: Guidance for clinicians