Department of Emergency Medicine, Lampang Hospital, Muang District, Lampang, Thailand.
Neurology Unit, Department of Internal Medicine, Center of Excellence in Stroke, Thammasat University, Pathum Thani Thailand.
PLoS One. 2019 Apr 10;14(4):e0214874. doi: 10.1371/journal.pone.0214874. eCollection 2019.
The standard treatment of acute ischemic stroke patients is thrombolytic therapy within 60 minutes of a patient's arrival in stroke center hospitals. Based on the policy of the Lampang Referral System Committee, blood samples of suspected stroke patients need to be collected before transfer to the stroke center (Lampang Hospital). It was still questionable as to whether these blood samples are valid for clinical use and the present study aimed to confirm or deny their validity.
A diagnostic study was conducted from June 2015 to May 2016. After exclusion, 340 patients were deemed eligible for analysis. Blood samples were collected just before normal saline infusion at referring hospitals and stored in blood collecting tube boxes set during transportation. At the stroke center, informed consents was requested, blood samples were re-collected to serve as a 'gold standard'. Prothrombin time (PT), international normalized ratio (INR), activated partial thromboplastin time (aPTT), platelet count, hemoglobin (Hb), hematocrit (Hct), blood urea nitrogen (BUN), and creatinine (Cr) were compared using paired t-tests. Binary regression was used to analyze for accuracy (%) to adjust for extraneous influences and was presented by modified Bland-Altman plots.
The laboratory results of referring hospitals vs. the stroke center were: PT, 12.4±3.2 vs. 12.5±3.0 sec; INR: 1.0±0.3 vs. 1.0±0.3; and platelet count: 239.8±77.1 vs. 239.8±74.8 (x103/μL). The adjusted accuracy of the PT, INR, and platelet counts were 96.8%, 96.8%, and 95.3% respectively.
Laboratory tests from referring hospital were determined to be valid. Blood samples should thus be collected at referring hospitals in order to avoid unnecessary blood collection at the stroke center.
急性缺血性脑卒中患者的标准治疗是在到达卒中中心医院 60 分钟内进行溶栓治疗。根据廊开转诊系统委员会的政策,疑似脑卒中患者的血液样本需要在转至卒中中心(廊开医院)之前采集。这些血液样本是否可用于临床仍然存在疑问,本研究旨在证实或否定其有效性。
本研究为 2015 年 6 月至 2016 年 5 月进行的一项诊断性研究。排除后,共有 340 例患者符合分析条件。在转诊医院采集血液样本,在采集前输注生理盐水,并储存在转运过程中设置的血液采集管盒中。在卒中中心,征得知情同意后,重新采集血液样本作为“金标准”。采用配对 t 检验比较凝血酶原时间(PT)、国际标准化比值(INR)、活化部分凝血活酶时间(aPTT)、血小板计数、血红蛋白(Hb)、红细胞压积(Hct)、血尿素氮(BUN)和肌酐(Cr)。采用二元回归分析校正准确性(%),并通过改良的 Bland-Altman 图进行呈现。
转诊医院与卒中中心的实验室结果如下:PT:12.4±3.2 秒比 12.5±3.0 秒;INR:1.0±0.3 比 1.0±0.3;血小板计数:239.8±77.1 比 239.8±74.8(x103/μL)。PT、INR 和血小板计数的校正准确性分别为 96.8%、96.8%和 95.3%。
来自转诊医院的实验室检测结果有效。因此,应在转诊医院采集血液样本,以避免在卒中中心进行不必要的血液采集。