Understanding histotripsy ablation safety: a systematic review of pre-clinical and clinical adverse events
Abstract
Abstract Histotripsy is the first cavitation-based ablation modality. Given limited clinical experience, synthesis of pre-clinical and early clinical data is essential to guide safe adoption. A PubMed and SCOPUS search was performed focused on pre-clinical and clinical adverse events (AEs) from Histotripsy ablation of parenchymal tissues in vivo ( n = 141 total studies, n = 27 clinical reports). Early data suggest an acceptable acute safety profile in select settings; however, reports of serious AEs including pre-clinical bowel perforations, clinical acute kidney injuries, clinical vascular injuries and thromboses, and a clinical case report of hyperprogression raise caution. These highlight the need for proper technique, understanding of mechanism nuances, and longer-term follow-up to assess effects. Recognition of mechanism-specific AEs provides a framework to guide future assessments and safer adoption of Histotripsy. Level of Evidence No level of evidence (review).
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Authors: Madeline I. Foo, Cynthia Uzoukwu, Robert Morhard, Katrina L. Falk, Bradford J. Wood, Gregory T. Frey, Timothy J. Ziemlewicz, Eli Vlaisavljevich, Beau Bosko Toskich, Alissa Hendricks-Wenger
Institutions: Johns Hopkins University, University of Wisconsin–Madison, University of Milan, Johns Hopkins Hospital, Virginia Tech, National Institutes of Health, Mayo Clinic in Florida, National Institutes of Health Clinical Center, Northeast Ohio Medical University