Assessment of adherence to diuretics and β-blockers by serum drug monitoring in comparison to urine analysis.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2020-10-01 Epub Date: 2020-05-13 DOI:10.1080/08037051.2020.1763775
Sabrina Ritscher, Coralie Georges, Cora Wunder, Pierre Wallemacq, Alexandre Persu, Stefan W Toennes
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引用次数: 4

Abstract

Purpose: Toxicological screenings for identifying antihypertensive drugs proved to be a useful tool for assessing adherence. However, misinterpretation may occur in case of highly metabolised drugs with low renal excretion, as well as for drugs with a prolonged detectability. The aim of the present study was to compare a recently developed therapeutic drug monitoring (TDM) method based on serum concentrations to an urine drug detection method for assessing adherence in outpatients.Materials and methods: Corresponding urine and blood samples were obtained at the same time from 26 outpatients without supervised medication. Urine and serum analyses were performed using established high-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) methodologies. Adherence was assumed if drugs were detectable in urine or if serum concentrations were above individually calculated lower dose-related concentrations (DRC) or literature-based therapeutic reference ranges (TRR) used as cut-off, respectively.Results: The identification of analytes in urine as well as the quantitative serum assay were performed for atenolol (n = 6 patients), bisoprolol (n = 8), nebivolol (n = 6), canrenone (n = 6, metabolite of spironolactone), hydrochlorothiazide (n = 12) and furosemide (n = 2). On the basis of drug detectability in urine, adherence was assumed in 88% of prescriptions. In 81% (DRC) and 50% (TRR) of the serum analyses the cut-off value was exceeded, which confirms patients' adherence in a lower number. Differences in adherence rates were found in five patients, mainly for β-blockers.Conclusion: This study suggests that assessment of adherence can be performed more precisely on the basis of serum drug concentrations with individually calculated lower DRC than by using the TRR or qualitative urinalysis.

通过血清药物监测和尿液分析来评估利尿剂和β-阻滞剂的依从性。
目的:毒理学筛查用于识别降压药已被证明是评估依从性的有用工具。然而,在肾排泄低的高代谢药物以及可检测时间较长的药物的情况下,可能会发生误解。本研究的目的是比较最近开发的基于血清浓度的治疗药物监测(TDM)方法与用于评估门诊患者依从性的尿液药物检测方法。材料与方法:对26例门诊无监护用药患者同时采集相应尿样和血样。尿液和血清分析采用已建立的高效液相色谱-串联质谱(LC-MS/MS)方法。如果尿液中检测到药物或血清浓度高于单独计算的低剂量相关浓度(DRC)或以文献为基础的治疗参考范围(TRR)作为截止值,则假设依从性。结果:对阿替洛尔(n = 6)、比索洛尔(n = 8)、奈比洛尔(n = 6)、卡乐酮(n = 6,螺内酯代谢物)、氢氯噻嗪(n = 12)、呋塞米(n = 2)进行了尿中分析物鉴定和血清定量分析。根据尿液中药物的可检出性,假设88%的处方遵医嘱。81% (DRC)和50% (TRR)的血清分析超过了临界值,这证实患者的依从性较低。5例患者的依从率存在差异,主要是β受体阻滞剂。结论:本研究表明,与使用TRR或定性尿液分析相比,基于单独计算的较低DRC的血清药物浓度可以更准确地评估依从性。
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
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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