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首页> 外文期刊>Journal of the American Society of Nephrology: JASN >Management of the waiting list for cadaveric kidney transplants: report of a survey and recommendations by the Clinical Practice Guidelines Committee of the American Society of Transplantation.
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Management of the waiting list for cadaveric kidney transplants: report of a survey and recommendations by the Clinical Practice Guidelines Committee of the American Society of Transplantation.

机译:尸体肾移植等待名单的管理:美国移植学会临床实践指南委员会的一项调查报告和建议。

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摘要

The Clinical Practice Guidelines Committee of the American Society of Transplantation developed a survey to review the policies of kidney transplant programs in the United States with respect to the management of the steadily expanding waiting list for cadaveric kidneys. The survey was sent to 287 centers, and 192 (67%) responded. The survey indicated that regular follow-up monitoring, most frequently on an annual basis, is required by the majority (71%) of programs. Patients considered to be at high risk and candidates for combined kidney-pancreas transplantation may be monitored more frequently. Annual screening for coronary artery disease is typically required for asymptomatic patients considered to be at high risk for covert disease. Noninvasive techniques are typically used, and a designated cardiologist is usually available to the transplant program. The dialysis nephrologist or the potential transplant recipient is expected to inform the transplant program of intercurrent events that may affect transplant candidacy. Standard health maintenance screening is required, together with the routine updating of serologic and other blood tests that may be relevant to the posttransplant course. Smaller transplant programs (<100 patients on the waiting list) are more likely to maintain closer contact with the wait-listed patients and to attempt to influence their treatment during dialysis and are less likely to cancel transplants because of unanticipated pretransplant medical problems. The work load necessitated by the follow-up monitoring of wait-listed patients was assessed and, in the absence of specific evidence-based information, a series of recommendations were developed to reflect current standards of practice and to suggest future research initiatives.
机译:美国移植学会的临床实践指南委员会开展了一项调查,以审查美国肾脏移植计划有关不断扩大的尸体肾脏等待名单管理的政策。该调查被发送到287个中心,有192个(67%)答复。调查表明,大多数(71%)计划都需要定期跟踪监测,最常见的是每年一次。被认为处于高风险的患者和可能联合进行肾胰移植的患者可能会受到更频繁的监测。对于无症状的隐性疾病高危患者,通常需要每年进行冠状动脉疾病筛查。通常使用非侵入性技术,并且指定的心脏病专家通常可用于移植程序。透析肾病学家或潜在的移植接受者应告知移植程序可能影响移植候选资格的并发事件。需要进行标准的健康维护筛查,并定期更新可能与移植后病程有关的血清学检查和其他血液检查。较小的移植计划(在等待名单上的患者少于100个)更可能与轮候名单上的患者保持密切联系,并试图影响他们在透析期间的治疗,并且由于未预料到的移植前医疗问题,取消移植计划的可能性也较小。评估了对等待入组患者进行随访监测所需的工作量,在缺乏具体的循证信息的情况下,制定了一系列建议以反映当前的实践标准并提出未来的研究计划。

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