A Service Evaluation of Anti-Xa Measurements in Patients with Kidney Impairment in a Tertiary Centre.

IF 2.3 4区 医学 Q2 UROLOGY & NEPHROLOGY
Nephron Pub Date : 2026-01-01 Epub Date: 2026-03-11 DOI:10.1159/000551515
Gerard Gurumurthy, Robyn Haysom, Mikias Lemma, Nadir Aziz, John Hartemink, Yasmin Begum, Jecko Thachil, Kathrine Parker
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引用次数: 0

Abstract

Background: Pre-emptive dose reduction of low-molecular-weight heparins (LMWHs) is often utilised in those with chronic kidney disease (CKD) to prevent bioaccumulation. We report on the association of a pre-emptive dose reduction on anti-Xa range and its correlation with clinical outcomes.

Methods: We undertook a retrospective service evaluation of patients with CKD (eGFR < 30 mL/min/1.73 m2) receiving therapeutic dose dalteparin. The primary exposure was dalteparin anti-Xa trough and peak. Primary outcomes were ISTH-defined clinically relevant bleeding, thrombosis, and all-cause mortality within 90 days of LMWH initiation. A multivariate Cox proportional hazards model was employed to assess the relationship between anti-Xa levels and the incidence of bleeding and mortality.

Results: A total of 103 patients were identified over a 2-year period. Seventy-eight (75.7%) had anti-Xa monitoring done. Trough anti-Xa distribution was within-target in 58 (75.6%). Patients on dialysis had a higher incidence of bleeding (19 vs. 12, p < 0.05). Patients with bleeding had significantly higher median anti-Xa trough (0.26 vs. 0.13 U/mL, p < 0.01). The median time to bioaccumulation was 19 days. In multivariate Cox models, only anti-Xa trough remained an independent association with bleeding (HR: 1.47 per 0.1 U/mL, 95% CI: 1.05-2.15; p < 0.05). No associations with mortality were identified.

Conclusion: In this report, trough anti-Xa measurement of dalteparin is independently associated with bleeding in patients with CKD. Further prospective, larger studies are warranted to validate these results before it can be universally recommended in clinical practice.

.

某三级医院肾损害患者抗xa检测服务评价。
背景:低分子肝素(LMWHs)的先发制人剂量减少通常用于慢性肾脏疾病(CKD)患者,以防止生物积累。我们报告了预防性剂量减少与抗xa范围的关联及其与临床结果的相关性。方法:对慢性肾病(eGFR < 30 ml/min/1.73m2)患者接受达特帕林治疗剂量进行回顾性服务评价。主要暴露为达特帕林抗xa波谷和峰。主要结局是低分子肝素起始90天内isth定义的临床相关出血、血栓形成和全因死亡率。采用多变量Cox比例风险模型评估抗xa水平与出血发生率和死亡率之间的关系。结果:两年内共发现103例患者。78例(75.7%)进行了抗xa监测。槽型抗xa分布在目标范围内58例(75.6%)。透析组患者出血发生率较高(19比12,p < 0.05)。出血组抗xa波谷中位数明显升高(0.26 vs 0.13 U/mL, p < 0.01)。生物积累的中位时间为19天。在多变量Cox模型中,只有抗xa槽与出血保持独立关联(HR: 1.47 / 0.1 U/mL, 95 % CI: 1.05-2.15;p < 0.05)。未发现与死亡率相关。结论:在本报告中,通过抗xa测量dalteparin与CKD患者出血独立相关。在临床实践中普遍推荐之前,需要进一步的前瞻性、更大规模的研究来验证这些结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nephron
Nephron UROLOGY & NEPHROLOGY-
CiteScore
5.00
自引率
0.00%
发文量
80
期刊介绍: ''Nephron'' comprises three sections, which are each under the editorship of internationally recognized leaders and served by specialized Associate Editors. Apart from high-quality original research, ''Nephron'' publishes invited reviews/minireviews on up-to-date topics. Papers undergo an innovative and transparent peer review process encompassing a Presentation Report which assesses and summarizes the presentation of the paper in an unbiased and standardized way.
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