Tomisin John

M.Flanagan, K.Kwan, T.John, et al., “Listening to the Patient Voice: Assessing Quality of Life and Anxiety Risk in Pediatric Liver Transplant Recipients,” Pediatric Transplantation30, no. 6 (2026): e70327, https://doi.org/10.1111/petr.70327. Conflicts of Interest The authors declare no conflicts of interest. Data Availability Statement The data that support the findings of this study are available from the corresponding author upon reasonable request.

1 Introduction Patient engagement in research involves a partnership between researchers, patients, and oftentimes, other knowledge users [1]. The Canadian Institute for Health Research Strategy for Patient-Oriented Research (CIHR-SPOR) defines patient engagement as the “meaningful and active collaboration in governance, priority setting, conducting research and knowledge translation” [1].