背景(考古学)
医学
肾移植
重症监护医学
生活质量(医疗保健)
癌症
移植
肾癌
相关性(法律)
内科学
护理部
古生物学
政治学
法学
生物
作者
Ellen Dobrijevic,Nicole Scholes‐Robertson,Chandana Guha,Martin Howell,Allison Jauré,Germaine Wong,Anita van Zwieten
标识
DOI:10.1016/j.semnephrol.2024.151499
摘要
Cancer has been identified by kidney transplant recipients as a critically important outcome. The co-occurrence of cancer and kidney transplantation represents a complex intersection of diseases, symptoms, and competing priorities for treatments. Research that focuses on biochemical parameters and clinical events may not capture the priorities of patients. Patient-centered research can improve the relevance and efficiency of research and is particularly pertinent in the setting of cancer and kidney transplantation to facilitate shared decision-making in complex clinical situations. In addition, patient-reported outcomes can facilitate the assessment of patients' experiences, symptom burden, treatment side effects, and quality of life. This review discusses patient-centered research in the context of kidney transplantation and cancer, including consumer involvement in research and patient-centered outcomes and their measures and inclusion in core outcome sets.
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