Karina Velásquez

Dr. Karina Velásquez


Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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31 January 2024 in Microorganisms
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Journal Article
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AGAndrea Gutierrez-Villanueva
Andrea Gutierrez-Villanueva
CQClaudia Quintana-Reyes
Claudia Quintana-Reyes
EAElena Martínez de Antonio
Elena Martínez de Antonio
BRBegoña Rodríguez-Alfonso
Begoña Rodríguez-Alfonso
KVKarina Velásquez
Karina Velásquez
Ana Fernández-CruzAna Fernández-Cruz
Ana Fernández-Cruz
Febrile neutropenia (FN) is a complication of hematologic malignancy therapy. An early diagnosis would allow optimization of antimicrobials. The 18F-FDG-PET-CT may be useful; however, its role is not well established. We analyzed retrospectively patients with hematological malignancies who underwent 18F-FDG-PET-CT as part of FN management in our university hospital and compared with conventional imaging. In addition, we performed a systematic review of the literature assessing the usefulness of 18F-FDG-PET-CT in FN. A total of 24 cases of FN underwent 18F-FDG-PET-CT. In addition, 92% had conventional CT. In 5/24 episodes (21%), the fever was of infectious etiology: two were bacterial, two were fungal, and one was parasitic. When compared with conventional imaging, 18F-FDG-PET-CT had an added value in 20 cases (83%): it diagnosed a new site of infection in 4 patients (17%), excluded infection in 16 (67%), and helped modify antimicrobials in 16 (67%). Antimicrobials could be discontinued in 10 (41.6%). We identified seven publications of low quality and one randomized trial. Our results support those of the literature. The available data suggest that 18F-FDG-PET-CT is useful in the management of FN, especially to diagnose fungal infections and rationalize antimicrobials. This review points out the low level of evidence and indicates the gaps in knowledge.

6 November 2026 in Preprints.org
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Preprint
Open access
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ASAlvaro Silva
Alvaro Silva
GRGabriela Rubial
Gabriela Rubial
LPLucía Pérez-Lamas
Lucía Pérez-Lamas
AGAndrea Gutierrez-Villanueva
Andrea Gutierrez-Villanueva
ATAna Alarcón Tomás
Ana Alarcón Tomás
Ana Fernández-CruzAna Fernández-Cruz
Ana Fernández-Cruz
Ruxolitinib is a JAK1 and JAK2 inhibitor approved in 2011 for the treatment of myelofibrosis., It is unclear if this drug can increase the risk of fungal infections. We present the case of a 67-year-old man with post-polycythemia vera myelofibrosis under treatment with ruxolitinib and azacitidine admitted to the Hematology Department with a history of subacute constitutional syndrome and diarrhea followed by fever. Biopsies of oral and colonic ulcerated lesions revealed Histoplasma; and subsequent bronchoalveolar lavage (BAL) was also positive for Histoplasma and Pneumocystis. Treatment with amphotericin B and isavuconazole was initiated without discontinuing ruxolitinib, resulting in a favourable response, confirmed by PET/CT. This case highlights the potential association of invasive fungal infection (IFI) with ruxolitinib treatment, the risk of endemic opportunistic fungal infections and the usefulness of PET/CT for follow-up of disseminated IFI.