Lorynn Teela

174 Chapter 6 38. van Cranenburgh, O. D., Ter Stege, J. A., de Korte, J., de Rie, M. A., Sprangers, M. A., & Smets, E. M. (2016). Patient-Reported Outcome Measurement in Clinical Dermatological Practice: Relevance and Feasibility of a Web-Based Portal. Dermatology, 232(1), 64-70, doi:10.1159/000440613. 39. van Rooijen, M., Lenzen, S., Dalemans, R., Moser, A., & Beurskens, A. (2020). Implementation of a Patient Reported Experience Measure in a Dutch disability care organisation: a qualitative study. J Patient Rep Outcomes, 4(1), 5, doi:10.1186/s41687-019-0169-3. 40. Pinto, C., Bristowe, K., Witt, J., Davies, J. M., de Wolf-Linder, S., Dawkins, M., et al. (2018). Perspectives of patients, family caregivers and health professionals on the use of outcome measures in palliative care and lessons for implementation: a multi-method qualitative study. Ann Palliat Med, 7(Suppl 3), S137-s150, doi:10.21037/apm.2018.09.02. 41. Christie, H. L., Bartels, S. L., Boots, L. M. M., Tange, H. J., Verhey, F. J. J., & de Vugt, M. E. (2018). A systematic review on the implementation of eHealth interventions for informal caregivers of people with dementia. Internet Interv, 13, 51-59, doi:10.1016/j.invent.2018.07.002. 42. Basch, E., Deal, A. M., Dueck, A. C., Scher, H. I., Kris, M. G., Hudis, C., et al. (2017). Overall Survival Results of a Trial Assessing Patient-Reported Outcomes for Symptom Monitoring During Routine Cancer Treatment. JAMA, 318(2), 197-198, doi:10.1001/jama.2017.7156. 43. Denis, F., Basch, E., Septans, A. L., Bennouna, J., Urban, T., Dueck, A. C., et al. (2019). Two-Year Survival Comparing Web-Based Symptom Monitoring vs Routine Surveillance Following Treatment for Lung Cancer. JAMA, 321(3), 306-307, doi:10.1001/jama.2018.18085. 44. van Muilekom, M. M., Teela, L., van Oers, H. A., Grootenhuis, M. A., & Haverman, L. (In progress). The use of the KLIK PROM portal in clinical care; the patients’ and parents’ point of view. 45. Engelen, V., van Zwieten, M. C. B., Koopman, H., Detmar, S., Caron, H., Brons, P., et al. (2012). The influence of patient reported outcomes on the discussion of psychosocial issues in children with cancer. Pediatric Blood & Cancer, 59(1), 161-166, doi:doi:10.1002/pbc.24089. 46. Schepers, S. A., Engelen, V. E., Haverman, L., Caron, H. N., Hoogerbrugge, P. M., Kaspers, G. J., et al. (2014). Patient reported outcomes in pediatric oncology practice: suggestions for future usage by parents and pediatric oncologists. Pediatr Blood Cancer, 61(9), 1707-1710, doi:10.1002/pbc.25034. 47. Schepers, S. A., Sint Nicolaas, S. M., Maurice-Stam, H., van Dijk-Lokkart, E. M., van den Bergh, E. M. M., de Boer, N., et al. (2017). First experience with electronic feedback of the Psychosocial Assessment Tool in pediatric cancer care. Support Care Cancer, doi:10.1007/s00520-017-3719-3. 48. Schepers, S. A., Sint Nicolaas, S. M., Maurice-Stam, H., Haverman, L., Verhaak, C. M., & Grootenhuis, M. A. (2018). Parental distress 6 months after a pediatric cancer diagnosis in relation to family psychosocial risk at diagnosis. Cancer, 124(2), 381-390, doi:10.1002/cncr.31023.

RkJQdWJsaXNoZXIy MTk4NDMw