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移植后肾性贫血:一项常规临床实践全国性研究发出的行动呼吁。

Post-transplant renal anemia: a call to action from a national study in routine clinical practice.

作者信息

Portoles Jose, Crespo Marta, Martínez Belotto Miguel, Martínez Morales Eduardo, Calatayud Aristoy Emma, Mora Lopez Paula, Garcia Sthefanny Carolina González, Oliveras Laia, Colina Julio, Singh Arhsdeep, Sancho Calabuig Asunción, Rodrigo Calabia Emilio, Montero Nuria, Gutierrez-Dalmau Alex, Mazuecos Auxiliadora, Pascual Julio

机构信息

Nephrology Department, Hospital Universitario Puerta de Hierro, IDIPHISA, Madrid, Spain.

Medicine Department, Facultad de Medicina, Universidad Autónoma de Madrid, IDIPHISA, Madrid, Spain.

出版信息

Clin Kidney J. 2024 Aug 30;17(10):sfae269. doi: 10.1093/ckj/sfae269. eCollection 2024 Oct.

DOI:10.1093/ckj/sfae269
PMID:39372236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11450472/
Abstract

BACKGROUND

Post-transplant anemia is a prevalent yet often overlooked condition that poses significant risks. Current guidelines consider the same treatment recommendations and goals for these patients as for chronic kidney disease patients not on dialysis. Previous reports demonstrated a lack of awareness and suboptimal management, indicating a pressing need for improvement. We therefore wanted to update the information on post-transplant anemia. We aimed to describe the present state of anemia management, goals and adherence to guidelines within a representative sample of the kidney transplant (KTx) population.

METHODS

We designed a retrospective nationwide multicenter study including outpatients from eight KTx hospitals. Nephrologists gathered data from electronic medical records encompassing demographics, comorbidities, KTx characteristics and immunosuppressive therapy, and information pertaining to anemia management (laboratory values, previously prescribed treatments and subsequent adjustments). The European statement on the Kidney Disease: Improving Global Outcomes (KDIGO) guidelines was the reference for definitions, drug prescriptions and targets. Anemia occurring within the initial 6 months post-transplantation was classified as early onset.

RESULTS

We included 297 patients with post-transplant anemia aged 62.8 years (standard deviation 13.6), 60% of whom were male. They had received a graft from cardiac death or brain death donors (61.6% and 31.1%, respectively) a median of 2.5 years (0.5-8.7) before. Among them 77% ( = 228) were classified as having late post-transplant anemia, characterized by a higher prevalence of microcytic and iron deficiency anemia. A total of 158 patients were on erythropoietic-stimulating agents (ESAs) treatment, yet surprisingly 110 of them lacked iron supplementation. Notably, 44 patients had an indication for iron supplementation and among them, 30 exhibited absolute iron deficiency. Out of the 158 patients receiving ESAs, only 39 surpassed the limit for the ESA resistance index, indicating poor response. This resistance was more frequent among patients with early post-transplant anemia (26.1% vs 9.2%). We have identified iron profile, early post-transplant anemia and estimated glomerular filtration rate as factors associated with the highest risk of resistance.

CONCLUSION

We found that hemoglobin targets are individualized upwards in post-transplant anemia. In this setting, iron therapy continues to be underutilized, especially intravenous, and iron deficiency and prior events (blood transfusion or hospital admission) explain most of the hyporesponsiveness to ESA. This highlights missed opportunities for precise prescription targeting and adherence to established guidelines, suggesting a need for improved management strategies in post-transplant anemia patients.

摘要

背景

移植后贫血是一种普遍存在但常被忽视的疾病,存在重大风险。当前指南对这些患者的治疗建议和目标与未接受透析的慢性肾病患者相同。先前的报告显示存在认识不足和管理欠佳的情况,表明迫切需要改进。因此,我们希望更新有关移植后贫血的信息。我们旨在描述肾移植(KTx)人群代表性样本中贫血管理的现状、目标及对指南的遵循情况。

方法

我们设计了一项全国性回顾性多中心研究,纳入来自八家KTx医院的门诊患者。肾病科医生从电子病历中收集数据,包括人口统计学、合并症、KTx特征和免疫抑制治疗,以及与贫血管理相关的信息(实验室检查值、先前开具的治疗及后续调整)。《肾脏病:改善全球预后(KDIGO)指南》作为定义、药物处方和目标的参考。移植后最初6个月内发生的贫血被归类为早期发生。

结果

我们纳入了297例移植后贫血患者,年龄62.8岁(标准差13.6),其中60%为男性。他们接受了来自心脏死亡或脑死亡供体的移植物(分别为61.6%和31.1%),中位时间为2.5年(0.5 - 8.7)。其中77%(n = 228)被归类为移植后晚期贫血,其特征是小细胞性贫血和缺铁性贫血的患病率较高。共有158例患者接受促红细胞生成素(ESA)治疗,但令人惊讶的是,其中110例未补充铁剂。值得注意的是,44例患者有补充铁剂的指征,其中30例表现为绝对缺铁。在接受ESA治疗的158例患者中,只有39例超过了ESA抵抗指数的限值,表明反应不佳。这种抵抗在移植后早期贫血患者中更常见(26.1%对9.2%)。我们确定铁代谢指标、移植后早期贫血和估计肾小球滤过率是与最高抵抗风险相关的因素。

结论

我们发现移植后贫血的血红蛋白目标是个体化上调的。在这种情况下,铁剂治疗仍未得到充分利用,尤其是静脉铁剂,缺铁和既往事件(输血或住院)解释了对ESA反应低下的大部分原因。这突出了精准处方靶向和遵循既定指南方面错失的机会,表明需要改进移植后贫血患者的管理策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e996/11450472/1bddd6d21775/sfae269fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e996/11450472/04c7219d7982/sfae269fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e996/11450472/1bddd6d21775/sfae269fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e996/11450472/04c7219d7982/sfae269fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e996/11450472/1bddd6d21775/sfae269fig2.jpg

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