Onuigbo Macaulay Amechi, Agbasi Nneoma
Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
Department of Nephrology, Mayo Clinic Health System, Eau Claire, Wisconsin, USA.
Hemodial Int. 2017 Oct;21 Suppl 2:S33-S40. doi: 10.1111/hdi.12597.
We first described the syndrome of rapid onset end stage renal disease (SORO-ESRD), acute yet irreversible renal failure, in 2010.
The impact of SORO-ESRD renal allograft survival remains speculative and we plan to study this question.
A retrospective analysis of individual adult patient-level serum creatinine trajectories of ESRD patients on maintenance hemodialysis for >90 days at Mayo Clinic, Rochester, 2001-2013.
Of 1461 ESRD patients, 149 (10%) patients including 13 renal transplant recipients (RTRs) satisfied the diagnosis of SORO-ESRD - 4 males, 9 females, 12 Caucasians/one other, age 45 (18-83) years. Serum creatinine was 1.4 (0.8-1.7) mg/dL in the last year before hemodialysis initiation. Initial hemodialysis access was a dialysis catheter in all 13 patients. AKI precipitating SORO-ESRD followed acute rejection (4), postoperative (2), tubulo-interstitial nephritis (2), unknown (2), infection/sepsis (1), contrast nephropathy (1), BKV nephropathy (1), and cardio-renal syndrome (1). Renal allograft survival was 1469 (277-4939) days (4 years). Renal allograft biopsies were available in 9/14 (69%) RTRs - Four showed acute rejection, two of which followed interruption of immunosuppression, three revealed acute tubular necrosis and four others also showed chronic transplant glomerulopathy. Time on hemodialysis was 856 (129-1630) days (2.4 years). 5/13 RTRs with SORO-ESRD (38%) died - 3 (60%) following cardiac arrest, 2 (40%) after stopping hemodialysis. 4/13 (31%) were re-transplanted in the period of this study.
SORO-ESRD contributed significantly to late renal allograft loss and return to hemodialysis with 100% initial dialysis catheter rate. Potentially preventable causes of AKI leading to SORO-ESRD were identified. The application of experience gained from such studies would help reduce late renal allograft loss and the need for re-transplantation. This would further help reduce the yawning gap between need and availability of donor kidney organs both here in the United States and around the world. Larger studies are warranted.
我们于2010年首次描述了快速进展至终末期肾病综合征(SORO-ESRD),即急性且不可逆的肾衰竭。
SORO-ESRD对肾移植受者的移植肾存活的影响仍不明确,我们计划研究这一问题。
对2001年至2013年在罗切斯特梅奥诊所接受维持性血液透析超过90天的成年终末期肾病患者的个体血清肌酐轨迹进行回顾性分析。
在1461例终末期肾病患者中,149例(10%)患者包括13例肾移植受者(RTRs)符合SORO-ESRD的诊断——4例男性,9例女性,12例白种人/1例其他种族,年龄45(18 - 83)岁。开始血液透析前最后一年的血清肌酐为1.4(0.8 - 1.7)mg/dL。所有13例患者最初的血液透析通路均为透析导管。导致SORO-ESRD的急性肾损伤(AKI)继发于急性排斥反应(4例)、术后(2例)、肾小管间质性肾炎(2例)、病因不明(2例)、感染/脓毒症(1例)、造影剂肾病(1例)、BK病毒肾病(1例)和心肾综合征(1例)。移植肾存活时间为1469(277 - 4939)天(4年)。14例RTRs中有9例(69%)可获得移植肾活检标本——4例显示急性排斥反应,其中2例继发于免疫抑制中断;3例显示急性肾小管坏死,另外4例还显示慢性移植肾小球病。血液透析时间为856(129 - 1630)天(2.4年)。13例患有SORO-ESRD的RTRs中有5例(38%)死亡——3例(60%)死于心脏骤停,2例(40%)在停止血液透析后死亡。在本研究期间,13例中有4例(31%)接受了再次移植。
SORO-ESRD是导致晚期移植肾丢失和恢复血液透析的重要原因,初始透析导管使用率达100%。已确定导致SORO-ESRD的AKI的潜在可预防病因。应用此类研究获得的经验将有助于减少晚期移植肾丢失和再次移植的需求。这将进一步有助于缩小美国及全球供肾器官需求与可获得性之间的巨大差距。有必要开展更大规模研究。