Division of Nephrology, Department of Medicine, Hatyai Hospital, Songkhla, Thailand.
Division of Nephrology, Department of Medicine, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, The Thai Red Cross Society, Bangkok, Thailand.
Syst Rev. 2024 Nov 12;13(1):278. doi: 10.1186/s13643-024-02709-8.
The effects of various risk and associated factors on post-kidney transplant anemia (PTA) have not been fully compared and estimated. This meta-analysis aims to elucidate factors contributing to PTA and determine the influence of erythropoietin-stimulating agents (ESAs) on renal outcomes, thus offering potential pathways for enhanced management strategies post-transplant.
A systematic review was conducted in electronical database. Studies reporting on risk factors (with cause-effect relationships) and associated factors (without definite cause-effect relationships) of PTA, and the effects of ESAs on post-kidney transplant outcomes, were included. Pooled odds ratios (ORs) and weighted mean differences (WMDs) were analyzed using random-effects models.
This systematic review encompassed 38,233 patients from 85 studies. Factors increased PTA risk included African American, older donor age, human antigen leukocyte mismatches, and low pre-transplant hemoglobin levels. Poor allograft function, high interleukine-6, Cytomegalovirus, delayed graft function, allograft rejections, immunosuppressive medications, and renin-angiotensin system blockades were associated with PTA. Native autosomal dominant polycystic kidney disease was a protective factor against PTA. Administration of ESAs with the aim of normalizing hemoglobin levels in patients with chronic allograft dysfunction slowed the decline in eGFR and reduce the risk of death, with a pooled OR of 0.36 (95% CI: 0.14 to 0.89; p = 0.040).
The risks and associated factors for PTA have been elucidated, underscoring the need for individualized treatment approaches. Late ESA therapy, aimed at hemoglobin normalization, suggests a renal-protective effect and reduced mortality, which should be considered in the management of PTA.
PROSPERO CRD42024545330.
各种风险因素及其相关因素对肾移植后贫血(PTA)的影响尚未得到充分比较和评估。本荟萃分析旨在阐明导致 PTA 的因素,并确定促红细胞生成素刺激剂(ESA)对肾移植结局的影响,从而为移植后提供潜在的强化管理策略途径。
系统检索电子数据库。纳入报告 PTA 的风险因素(具有因果关系)和相关因素(无明确因果关系),以及 ESA 对肾移植后结局影响的研究。采用随机效应模型分析汇总优势比(OR)和加权均数差(WMD)。
本系统综述纳入了来自 85 项研究的 38233 名患者。增加 PTA 风险的因素包括非裔美国人、供体年龄较大、人类白细胞抗原错配和移植前血红蛋白水平较低。移植物功能不良、白细胞介素-6、巨细胞病毒、延迟移植物功能、移植物排斥反应、免疫抑制药物和肾素-血管紧张素系统阻滞剂与 PTA 相关。原发性常染色体显性多囊肾病是 PTA 的保护因素。为纠正慢性移植物功能障碍患者的血红蛋白水平而给予 ESA 治疗可减缓 eGFR 下降速度并降低死亡风险,汇总 OR 为 0.36(95%CI:0.14 至 0.89;p=0.040)。
阐明了 PTA 的风险和相关因素,强调了个体化治疗方法的必要性。旨在使血红蛋白正常化的晚期 ESA 治疗提示具有肾脏保护作用和降低死亡率,在 PTA 的管理中应考虑这一点。
PROSPERO CRD42024545330。