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急性中风与心房颤动:仅根据血浆肌酐估算肾功能时新型口服抗凝药剂量错误的风险

Acute Stroke and Atrial Fibrillation: Risk of Incorrect NOAC Dosage When Estimating Renal Function From Plasma Creatinine Only.

作者信息

Amoey Danial C, Thranitz Julia, Münte Thomas F, Royl Georg

机构信息

Department of Neurology, University of Lübeck, Lübeck, Germany.

Center of Brain, Behavior and Metabolism, University of Lübeck, Lübeck, Germany.

出版信息

Front Neurol. 2022 Jul 5;13:907912. doi: 10.3389/fneur.2022.907912. eCollection 2022.

Abstract

BACKGROUND

Cardioembolic stroke (CS) due to atrial fibrillation (AF) bears a high risk of unfavorable outcome. Treatment with a non-vitamin K antagonist oral anticoagulant (NOAC) reduces this risk. NOAC dosage occurs on a thin line during the acute phase of the stroke unit when the patient is threatened by both recurrent CS and a hemorrhagic stroke. It is often adapted to renal function-usually glomerular filtration rate (GFR)-to prevent both under- and overdosing. This study investigates the hypothetical risk of incorrect NOAC dosage after acute stroke when relying on plasma creatinine alone in comparison to a more exact renal function assessment including urine collection.

METHODS

In a cohort study on consecutive 481 patients treated in a stroke unit with acute stroke and AF, the GFR estimated from plasma creatinine (eGFR) was compared to concurrent creatinine clearance measurement (CrCl) from urine collection regarding the hypothetically derived NOAC dosage.

RESULTS

The risk of incorrect dosage (mean, 95% confidence interval) was 6.9% (4.8-9.5), 26% (23-31), 38% (33-42), and 20% (16-23) for apixaban, dabigatran, edoxaban, and rivaroxaban, respectively. The overall risk for incorrect dosage of any NOAC was 23% (21-25). Thresholds for age and admission eGFR were optimized to achieve an overall risk below 5% by additional CrCl measurements in selected patients (apixaban <36 ml/min and any age, dabigatran <75 ml/min and >70 y, edoxaban >36 ml/min and >58 y, rivaroxaban <76 ml/min and >75 y, any NOAC <81 ml/min and >54 y). The resulting portion of patients requiring an additional CrCl measurement was 10, 60, 80, 55, and 65% for apixaban, dabigatran, edoxaban, rivaroxaban, and any NOAC, respectively.

CONCLUSIONS

There is a considerable risk of incorrect NOAC dosage in patients with acute CS treated in a stroke unit that can be lowered by targeted CrCl measurements in selected patients.

摘要

背景

心房颤动(AF)所致的心源性栓塞性卒中(CS)预后不良风险高。使用非维生素K拮抗剂口服抗凝药(NOAC)治疗可降低此风险。在卒中单元急性期,当患者面临复发性CS和出血性卒中双重威胁时,NOAC的剂量调整十分微妙。其剂量通常根据肾功能——通常是肾小球滤过率(GFR)——进行调整,以防止剂量不足和过量。本研究调查了急性卒中后仅依靠血肌酐与采用包括尿液收集在内的更精确肾功能评估相比,NOAC剂量错误的假设风险。

方法

在一项对481例在卒中单元接受急性卒中和AF治疗的连续患者的队列研究中,将根据血肌酐估算的GFR(eGFR)与同时进行的尿液收集肌酐清除率测量(CrCl)在假设的NOAC剂量方面进行比较。

结果

阿哌沙班、达比加群、依度沙班和利伐沙班剂量错误的风险(均值,95%置信区间)分别为6.9%(4.8 - 9.5)、26%(23 - 31)、38%(33 - 42)和20%(16 - 23)。任何NOAC剂量错误的总体风险为23%(21 - 25)。通过对选定患者进行额外的CrCl测量,优化年龄和入院时eGFR的阈值,以使总体风险低于5%(阿哌沙班<36 ml/min且任何年龄,达比加群<75 ml/min且>70岁,依度沙班>36 ml/min且>58岁,利伐沙班<76 ml/min且>75岁,任何NOAC<81 ml/min且>54岁)。阿哌沙班、达比加群、依度沙班、利伐沙班和任何NOAC分别需要进行额外CrCl测量的患者比例为10%、60%、80%、55%和65%。

结论

在卒中单元接受治疗的急性CS患者中,NOAC剂量错误的风险相当大,通过对选定患者进行有针对性的CrCl测量可降低该风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c62/9294157/c7a866861816/fneur-13-907912-g0001.jpg

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