Audrey L'Espérance

Dumez, V., & L’Espérance, A. (2024). Beyond experiential knowledge : A classification of patient knowledge. Social Theory & Health, 22(3), 173‑186. 

Calderon Ramirez, C., Farmer, Y., Frolic, A., Bravo, G., Gaucher, N. O., Payot, A., Opatrny, L., Poirier, D., Dahine, J., L’Espérance, A., Downar, J., Tanuseputro, P., Rousseau, L.-M., Dumez, V., Descôteaux, A., Dallaire, C., Laporte, K., & Bouthillier, M.-E. (2024). What are the views of Quebec and Ontario citizens on the tiebreaker criteria for prioritizing access to adult critical care in the extreme context of a COVID-19 pandemic? BMC Medical Ethics, 25(1), 31. 

Pomey, M., Pelaez, S., Le Roux, E., Demers‐Payette, O., Sirois, M., Lochhead, L., Ganache, I., Normandin, L., L’Espérance, A., & de Guise, M. (2024). How to mobilise users’ experiential knowledge in the evaluation of advanced technologies and practices in Quebec? The example of the permanent users’ and relatives’ panel. Health Expectations : An International Journal of Public Participation in Health Care and Health Policy, 27(1), e13964.

Chudyk, A. M., Stoddard, R., Duhamel, T. A., Patient Engagement in Research Partners, Andreas, B., Ashe, M. C., Daly-Cyr, J., Elliott, S., L’Espérance, A., Park, M., Parry, M., Puts, M., Rich, M., Robinson, B., Rubenstein, D., Sanchez, S., Schreiner, K., Singer-Norris, L., Smith, K., & Strudwick, G. (2024). Future directions for patient engagement in research : A participatory workshop with Canadian patient partners and academic researchers. Health Research Policy & Systems, 22(1), 1‑15. 

Getchell, L. E., Reich, M., Allu, S., Woods, C., Atkinson, T., Beaucage, M., Stalker, L., Sparkes, D., Turner, C., L’Esperance, A., Burns, K., Elliott, M. J., Chiu, H., Rosenblum, N. D., & Sapir-Pichhadze, R. (2023). Storytelling for impact : The creation of a storytelling program for patient partners in research. Research Involvement and Engagement, 9(1), 57. 

Menear, M., Duhoux, A., Bédard, M., Paquette, J.-S., Baron, M., Breton, M., Courtemanche, S., Dubé, S., Dufour, S., Fortin, M., Girard, A., Larouche-Côté, É., L’Espérance, A., LeBlanc, A., Poitras, M.-E., Rivet, S., Sasseville, M., Achim, A., Archambault, P., … Wong, S. (2023). Understanding the impacts of the COVID-19 pandemic on the care experiences of people with mental-physical multimorbidity : Protocol for a mixed methods study. BMC primary care, 24(1), 154. 

Getchell, L. E., Fowler, E., Reich, M., Allu, S., Boucher, C., Burns, K., Desjarlais, A., L’Espérance, A., Elliott, M., Robinson-Settee, H., Chiu, H. H.-L., Rosenblum, N. D., Settee, C., Murdoch, A., Dew, S., Green, A., Franson, L., Bernstein, E., Sparkes, D., … Sapir-Pichhadze, R. (2022). Program Report : Can-SOLVE CKD Network Presents an Inclusive Method for Developing Patient-Oriented Research Tools. Canadian Journal of Kidney Health and Disease, 9. 

Pomey, M.-P., Bush, P. L., Demers-Payette, O., L’Espérance, A., Lochhead, L., Ganache, I., & Roy, D. (2021). Developing recommendations for the diagnosis and treatment of Lyme disease : The role of the patient’s perspective in a controversial environment. International Journal of Technology Assessment in Health Care, 37(1), e11. 

L’Espérance, A., O’Brien, N., Grégoire, A., Abelson, J., Canfield, C., Grande, C. D., Dogba, M. J., Fancott, C., Levasseur, M. A., Loignon, C., Majnemer, A., Pomey, M.-P., Rasiah, J., Salsberg, J., Santana, M., Tremblay, M.-C., Urquhart, R., & Boivin, A. (2021). Developing a Canadian evaluation framework for patient and public engagement in research : Study protocol. Research Involvement and Engagement, 7(1), 1‑12. 

L’Espérance, A. (2019). Jeter des ponts entre l’expertise et l’expérience en PMA. Policy Options. 

Vous trouverez l'ensemble des publications sur le site de la Bibliothèque.