Problematic issues of optimizing the transfer of renal transplant recipients from pediatric to adult health care (literature review)

O. V. Raikevich-Liachovskaya, A. V. Sukalo, S. V. Baiko
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Abstract

The transfer of kidney transplant recipients from pediatric to adult healthcare should be a planned process, as it involves various risks, including loss of the transplanted organ and death of the patient. The most critical age for the development of adverse events is the age of 17–24 years. This is because of the peculiarities of the maturation of the brain of adolescents, severe kidney disease and the need for constant medication. At this age, patients experience peer pressure, preoccupation with their appearance, personal development, pursuits and dreams for the future, which may not come true against the background of a long-term chronic illness and lead to low self-esteem, depression and anger. The result of these psycho-emotional experiences may be non-compliance with the regimen of immunosuppressive drugs with the development of rejection, and even loss of a kidney transplant. The transition process should ideally take several years and start early, usually between the ages of 12 and 14. The transfer should be carried out not only after the onset of a certain age, but also based on the existing skills and readiness of the patient. The patient must remain in the pediatric service if severe complications (rejection, infections) develop until they are treated and for at least 1 year after transplantation, even if this period is the age of transition to adult service. Following a transition readiness assessment, a structured plan should be drawn up requiring the integration of medical, educational, behavioral and social strategies both during and after the transition. Establishing transitional clinics or assigning a position of coordinator allows controlling the transition process and minimize possible risks and negative consequences. The development and implementation of programs for the transition of kidney transplant recipients to adult service are aimed at increasing the survival of the kidney transplant and patients, improving their quality of life.
优化肾移植受者从儿科转移到成人医疗保健的问题(文献综述)
肾移植受者从儿科转移到成人医疗机构应该是一个有计划的过程,因为它涉及各种风险,包括移植器官的丢失和患者的死亡。不良事件发生的最关键年龄是17-24岁。这是由于青少年大脑发育成熟的特点、严重的肾脏疾病以及需要持续用药。在这个年龄段,患者会经历同伴压力,关注自己的外表、个人发展、追求和对未来的梦想,而这些在长期慢性疾病的背景下可能无法实现,从而导致自卑、抑郁和愤怒。这些心理-情绪体验的结果可能是不遵守免疫抑制药物的治疗方案,并发展为排斥反应,甚至失去肾移植。理想情况下,这个转变过程应该持续几年,并且尽早开始,通常在12岁到14岁之间。转移不仅要在发病某一年龄后进行,而且要根据患者的现有技能和准备情况进行。如果出现严重并发症(排斥反应、感染),患者必须留在儿科服务,直到接受治疗,并且移植后至少1年,即使这段时间是向成人服务过渡的年龄。在对过渡准备情况进行评估之后,应制定一项有组织的计划,要求在过渡期间和之后将医疗、教育、行为和社会战略结合起来。建立过渡诊所或指定一个协调员的职位可以控制过渡过程,最大限度地减少可能的风险和负面后果。肾移植受者向成人服务过渡的项目的制定和实施旨在提高肾移植和患者的存活率,提高他们的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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