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Arora, Satyam

https://orcid.org/0000-0002-9048-5624

Mayo Clinic

Postgraduate Institute of Child Health Noida India

Citations 2

Artificial intelligence and transfusion education, research and practice: The view from the ISBT Clinical Transfusion Working Party
Al‐Riyami, Arwa Z. , Gammon, Richard R. , Seheult, Jansen N. , Arora, Satyam , Goel, Ruchika , Seheult, Jansen, Goel, Ruchika , Gammon, Richard R , Seheult, Jansen N , Arora, Satyam

Vox Sanguinis | January 19, 2025 | Volume: 121 | Issue: 4 | Pages: 481-487

10.1111/vox.13793 Get It

Abstract Background and Objectives Artificial intelligence (AI) has been gaining increasing interest in healthcare. During the 2024 International Society of Blood Transfusion (ISBT) Congress, the Clinical Transfusion Working Party (CTWP) conducted a session to explore the exciting intersection of AI in transfusion medicine (TM) practice, education and research. We report here the potential applications and the session outcome. Materials and Methods A pre‐workshop survey explored the participants' demographics and areas of use of AI and whether they have had any AI‐specific training or education. The workshop included presentations on the regulatory aspects of AI use and its application in TM practice, education and research. These were followed by round‐table discussions to explore participants' experience and concerns. Results The workshop had 72 attendees, with 38% falling in the 36–45‐year age group. A total of 70% indicated the use of AI, but only 12% reported having specific training or education. Participants expressed interest in different potential applications but also shared concerns on over‐reliance, potential loss of skills, the accuracy of provided information and content plagiarism. Conclusion The findings of the workshop highlight the need for training, educational resources, standards and regulatory frameworks to guide the use of AI tools in the field of TM.
Multi‐institutional experience with COVID‐19 convalescent plasma in children
Jacquot, Cyril , Noland, Daniel K., Donowitz, Jeffrey R. , Levy, Emily R. , Willis, Zachary , Rimland, Casey A. , Loi, Michele , Arrieta, Antonio , Drapeau, Noelle, Osborne, Stephanie , Zivick, Elise, Delaney, Meghan , Levy, Emily R , Arora, Satyam , Delaney, Meghan , Jacquot, Cyril , Gordon, Oren M. , Jain, Sanjay K. , Annen, Kyle , Ardura, Monica I. , Arora, Satyam

Transfusion | March 25, 2023 | Volume: 63 | Issue: 5 | Pages: 918-924

10.1111/trf.17318 Get It

AbstractBackground and ObjectivesConvalescent COVID‐19 plasma (CCP) was developed and used worldwide as a treatment option by supplying passive immunity. Adult studies suggest administering high‐titer CCP early in the disease course of patients who are expected to be antibody‐negative; however, pediatric experience is limited. We created a multi‐institutional registry to characterize pediatric patients (<18 years) who received CCP and to assess the safety of this intervention.MethodsA REDCap survey was distributed. The registry collected de‐identified data including demographic information (age, gender, and underlying conditions), COVID‐19 disease features and concurrent treatments, CCP transfusion and safety events, and therapy response.ResultsNinety‐five children received CCP: 90 inpatients and 5 outpatients, with a median age of 10.2 years (range 0–17.9). They were predominantly Latino/Hispanic and White. The most frequent underlying medical conditions were chronic respiratory disease, immunosuppression, obesity, and genetic syndromes. CCP was primarily given as a treatment (95%) rather than prophylaxis (5%). Median total plasma dose administered and transfusion rates were 5.0 ml/kg and 2.6 ml/kg/h, respectively. The transfusions were well‐tolerated, with 3 in 115 transfusions reporting mild reactions. No serious adverse events were reported. Severity scores decreased significantly 7 days after CCP transfusion or at discharge. Eighty‐five patients (94.4%) survived to hospital discharge. All five outpatients survived to 60 days.ConclusionsCCP was found to be safe and well‐tolerated in children. CCP was frequently given concurrently with other COVID‐19‐directed treatments with improvement in clinical severity scores ≥7 days after CCP, but efficacy could not be evaluated in this study.