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引用次数: 0

摘要

移植协调杂志,第9卷,第3期,1999年9月存活率在过去十年中也有所提高。从1986年到1993年,尸体移植的中位生存期从5.4年增加到8.5年,而活体移植的中位生存期从9.7年增加到14.7年排除移植物功能正常导致的死亡,慢性排斥反应是晚期移植物损失的主要原因慢性排斥反应的危险因素包括急性排斥反应史、免疫抑制不足、移植物功能延迟、急性肾小管坏死、供体器官特征(如年龄0 ~ 60岁、尸体供体与活体供体)、受体特征(如性别和年龄)、移植前疾病(如糖尿病和高血压)和感染因此,移植受者的临床管理应包括预防慢性排斥反应发展的策略,从而提高移植的长期存活率。随着免疫疗法的选择越来越多,移植受者将继续体验到更好的短期和长期结果。可用的免疫抑制剂名单继续扩大(表1),其他一些有前途的新药正在研究中。虽然新的组合正在测试中,目前最佳的免疫抑制方案仍然主要是钙调磷酸酶抑制剂为主。环孢素药物替代的问题:对患者管理的影响
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Issues in Cyclosporine Drug Substitution: Implications for Patient Management
Journal of Transplant Coordination, Vol. 9, Number 3, September 1999 survival rates have also improved in the past decade. Between 1986 and 1993, median cadaveric graft survival increased from 5.4 years to 8.5 years, whereas median live donor graft survival increased from 9.7 years to 14.7 years.3 Excluding death with a functioning graft, chronic rejection accounts for the majority of late graft losses.4 Risk factors for chronic rejection include history of acute rejection, inadequate immunosuppression, delayed graft function, acute tubular necrosis, donor organ characteristics (eg, age >60 years and cadaveric vs live donor), recipient characteristics (eg, gender and age), pretransplantation diseases (eg, diabetes and hypertension), and infection.5 Clinical management of the transplant recipient should therefore include strategies to prevent the development of chronic rejection, thereby improving long-term graft survival. As more options for immunotherapy become available, transplant recipients will continue to experience better short-term and long-term outcomes. The list of available immmunosuppressants continues to expand (Table 1) and several other promising new agents are under investigation. Although new combinations are being tested, the current optimal immunosuppressive regimen remains predominantly calcineurin-inhibitor based. Issues in cyclosporine drug substitution: implications for patient management
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