• Abigail Baim-Lance, Katelyn B Ferreira, Harvey Jay Cohen, Susan S Ellenberg, George A Kuchel, Christine Ritchie, Greg A Sachs, Dalane Kitzman, R Sean Morrison, and Albert Siu.
• Brookdale Department of Geriatrics and Palliative Medicine, Icahn School of Medicine at Mount Sinai, One Gustave L Levy Place, Box 1070, New York, NY, 10029, USA. Abigail.baim-lance@mssm.edu.
• J Gen Intern Med. 2023 Feb 1; 38 (2): 399405399-405.

BackgroundClinical trials are needed to study topics relevant to older adults with serious illness. Investigators conducting clinical trials with this population are challenged by how to appropriately define, classify, report, and monitor serious and non-serious adverse events (SAEs/AEs), given that some traditionally reported AEs (pressure ulcers, delirium) and SAEs (death, hospitalization) are common in persons with serious illness, and may be consistent with their goals of care.ObjectivesA multi-stakeholder group convened to establish greater clarity on and new approaches to address this critical issue.ParticipantsThirty-two study investigators, members of regulatory and sponsor agencies, and patient stakeholders took part.ApproachThe group met virtually four times and, using a collaborative approach, conducted a survey, select interviews, and reviewed regulatory guidance to collectively define the problem and identify a new approach.ResultsSAE/AE challenges fell into two areas: (1) definitions and classifications, including (a) implausible relationships, (b) misalignment with patient-centered care goals, and (c) well-known associations, and (2) reporting and monitoring, including (a) limited guidance, (b) inconsistent standards across regulators, and (c) Data Safety Monitoring Board (DSMB) member knowledge gaps. Problems largely reflected practice norms rather than regulatory requirements that already support context-specific and aggregate reporting. Approaches can be improved by adopting principles that better align strategies for addressing adverse events with the type of intervention being tested, favoring routine and aggregate over expedited reporting, and prioritizing how SAE/AEs relate to patient-centered care goals. Reporting plans and decisions should follow an algorithm underpinned by these principles.ConclusionsAdoption of the proposed approach-and supporting it with education and better alignment with regulatory guidance and procedures-could improve the quality and efficiency of clinical trials' safety involving older adults with serious illness and other vulnerable populations.© 2022. This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply.

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