van der Schaar J A J, Attema-de Jonge M E, Gresnigt F M J, Franssen E J F
Department of Clinical Pharmacy, OLVG, Amsterdam, The Netherlands.
Emergency Department, OLVG, Amsterdam, The Netherlands.
Toxicol Rep. 2020 Apr 20;7:539-546. doi: 10.1016/j.toxrep.2020.04.007. eCollection 2020.
For diagnosis and treatment in the acute setting, it is crucial to know whether the clinical status of patients might be explained by the effects of drugs.The objective of this study was to determine how many drugs were detected by comprehensive toxicological screening, that could not be detected with a routine drugs-of-abuse point-of-care test (DOA-POCT) and which drugs of abuse (DOA) were relevant. A secondary objective was to determine in how many patients comprehensive toxicological screening provided additional clinically relevant information.
In this prospective study, patients were included in whom a DOA-POCT was performed and residual urine and serum samples were available.DOA-POCT were performed using the Triage® TOX Drug Screen. Comprehensive toxicological screening was performed using 1) the Toxtyper™ LC-MS method and 2) two GC-FID methods for alcohols and GHB respectively.The clinical relevance of the comprehensive toxicological screening results regarding diagnosis and patient management was quantified.
A total of 100 patients were included. In 91 of these patients, comprehensive toxicological screening identified 234 drugs that were not identified by DOA-POCT. However, DOA-POCT identified 34 DOA that were not identified by comprehensive toxicological screening.Seven percent of comprehensive toxicological screening results were found to be clinically relevant, all with regard to diagnosis. GHB and ketamine were the drugs involved. Another 38 % strengthened confidence in diagnosis and patient care decisions.
GHB and ketamine should be added to the panel of drugs we screen at the point of care in the Amsterdam acute setting.
在急性情况下进行诊断和治疗时,了解患者的临床状况是否可能由药物作用引起至关重要。本研究的目的是确定通过全面毒理学筛查检测到的、常规滥用药物即时检验(DOA-POCT)无法检测到的药物数量,以及哪些滥用药物(DOA)是相关的。次要目的是确定全面毒理学筛查在多少患者中提供了额外的临床相关信息。
在这项前瞻性研究中,纳入了进行了DOA-POCT且有残余尿液和血清样本的患者。使用Triage® TOX药物筛查进行DOA-POCT。使用1)Toxtyper™ LC-MS方法和2)分别用于酒精和γ-羟基丁酸(GHB)的两种气相色谱-火焰离子化检测(GC-FID)方法进行全面毒理学筛查。对全面毒理学筛查结果在诊断和患者管理方面的临床相关性进行了量化。
共纳入100例患者。在其中91例患者中,全面毒理学筛查鉴定出234种DOA-POCT未鉴定出的药物。然而,DOA-POCT鉴定出34种全面毒理学筛查未鉴定出的DOA。发现7%的全面毒理学筛查结果具有临床相关性,均与诊断有关。涉及的药物为GHB和氯胺酮。另外38%增强了对诊断和患者护理决策的信心。
在阿姆斯特丹急性情况下的即时护理中,应将GHB和氯胺酮添加到我们筛查的药物清单中。