Capoor Manu N, Stonemetz Jerry L, Baird John C, Ahmed Fahad S, Awan Ahsan, Birkenmaier Christof, Inchiosa Mario A, Magid Steven K, McGoldrick Kathryn, Molmenti Ernesto, Naqvi Sajjad, Parker Stephen D, Pothula S M, Shander Aryeh, Steen R Grant, Urban Michael K, Wall Judith, Fischetti Vincent A
Department of Bacterial Pathogenesis and Immunology, Rockefeller University, New York, New York, United States of America; MMF Systems, Inc., New York, New York, United States of America.
Department of Anesthesia, The Johns Hopkins Hospital, Baltimore, Maryland, United States of America.
PLoS One. 2015 Aug 11;10(8):e0133317. doi: 10.1371/journal.pone.0133317. eCollection 2015.
A substantial fraction of all American healthcare expenditures are potentially wasted, and practices that are not evidence-based could contribute to such waste. We sought to characterize whether Prothrombin Time (PT) and activated Partial Thromboplastin Time (aPTT) tests of preoperative patients are used in a way unsupported by evidence and potentially wasteful.
We evaluated prospectively-collected patient data from 19 major teaching hospitals and 8 hospital-affiliated surgical centers in 7 states (Delaware, Florida, Maryland, Massachusetts, New Jersey, New York, Pennsylvania) and the District of Columbia. A total of 1,053,472 consecutive patients represented every patient admitted for elective surgery from 2009 to 2012 at all 27 settings. A subset of 682,049 patients (64.7%) had one or both tests done and history and physical (H&P) records available for analysis. Unnecessary tests for bleeding risk were defined as: PT tests done on patients with no history of abnormal bleeding, warfarin therapy, vitamin K-dependent clotting factor deficiency, or liver disease; or aPTT tests done on patients with no history of heparin treatment, hemophilia, lupus anticoagulant antibodies, or von Willebrand disease. We assessed the proportion of patients who received PT or aPTT tests who lacked evidence-based reasons for testing.
This study sought to bring the availability of big data together with applied comparative effectiveness research. Among preoperative patients, 26.2% received PT tests, and 94.3% of tests were unnecessary, given the absence of findings on H&P. Similarly, 23.3% of preoperative patients received aPTT tests, of which 99.9% were unnecessary. Among patients with no H&P findings suggestive of bleeding risk, 6.6% of PT tests and 7.1% of aPTT tests were either a false positive or a true positive (i.e. indicative of a previously-undiagnosed potential bleeding risk). Both PT and aPTT, designed as diagnostic tests, are apparently used as screening tests. Use of unnecessary screening tests raises concerns for the costs of such testing and the consequences of false positive results.
美国所有医疗保健支出中有很大一部分可能被浪费了,而那些缺乏循证依据的医疗行为可能导致了这种浪费。我们试图确定术前患者的凝血酶原时间(PT)和活化部分凝血活酶时间(aPTT)检测是否以缺乏循证依据且可能造成浪费的方式被使用。
我们评估了来自特拉华州、佛罗里达州、马里兰州、马萨诸塞州、新泽西州、纽约州、宾夕法尼亚州7个州以及哥伦比亚特区的19家主要教学医院和8家医院附属外科中心前瞻性收集的患者数据。总共1,053,472例连续患者代表了2009年至2012年期间在所有这27个机构接受择期手术的每一位患者。682,049例患者(64.7%)的子集进行了一项或两项检测,并拥有可用于分析的病史和体格检查(H&P)记录。针对出血风险的不必要检测被定义为:对没有异常出血史、未接受华法林治疗、不存在维生素K依赖凝血因子缺乏或肝病的患者进行PT检测;或者对没有肝素治疗史、血友病、狼疮抗凝抗体或血管性血友病的患者进行aPTT检测。我们评估了接受PT或aPTT检测但缺乏循证检测理由的患者比例。
本研究旨在将大数据的可用性与应用比较效果研究结合起来。在术前患者中,26.2%接受了PT检测,鉴于H&P检查未发现相关结果,94.3%的检测是不必要的。同样,23.3%的术前患者接受了aPTT检测,其中99.9%是不必要的。在没有H&P检查结果提示出血风险的患者中,6.6%的PT检测和7.1%的aPTT检测要么是假阳性,要么是真阳性(即表明存在先前未诊断出的潜在出血风险)。PT和aPTT作为诊断检测,显然被用作筛查检测。使用不必要的筛查检测引发了对这种检测成本以及假阳性结果后果的担忧。