Cook Janine D, Strauss Kathy A, Caplan Yale H, Lodico Charles P, Bush Donna M
Department of Pathology, Mercy Medical Center, Baltimore, Maryland 21202, USA.
J Anal Toxicol. 2007 Oct;31(8):486-96. doi: 10.1093/jat/31.8.486.
The Mandatory Guidelines for Federal Workplace Drug Testing Programs provide criteria for specimen validity testing, including urine pH cut-offs, to report a urine specimen as adulterated or invalid. Since the urine pH criteria for invalid classifications, > or = 3 and < 4.5 or > or = 9 and < 11, became effective in November 2004, a number of specimens with results within the upper invalid limits, typically in the range of 9.1 to 9.3, have been reported with no evidence of adulteration. This study evaluated the hypothesis that these pH findings were the result of exposure to increased environmental temperatures during specimen standing and transport. Indeed, increased storage temperatures were associated with increased urine pH, with the magnitude of the change related to both storage time and temperature. The pH values of specimens stored at -20 degrees C are relatively stable, whereas pH results > 9 are achieved at storage temperatures of room temperature or higher. It is noteworthy that no condition(s) produced a specimen with a pH > 9.5. Degradation of nitrogenous urine analytes is most likely responsible for the noted increases in pH. These findings are intended to supplement information used by the Medical Review Officers who are responsible for interpreting such marginally invalid pH results.
《联邦工作场所药物检测计划强制指南》规定了样本有效性检测的标准,包括尿液pH值临界值,用于报告尿液样本是否被掺假或无效。自2004年11月无效分类的尿液pH值标准(≥3且<4.5或≥9且<11)生效以来,已报告了一些结果处于较高无效限值范围内(通常在9.1至9.3之间)的样本,且无掺假证据。本研究评估了以下假设:这些pH值结果是样本静置和运输过程中环境温度升高所致。事实上,储存温度升高与尿液pH值升高相关,变化幅度与储存时间和温度均有关。储存在-20℃的样本pH值相对稳定,而在室温或更高储存温度下pH值结果会>9。值得注意的是,没有任何情况会使样本pH值>9.5。含氮尿液分析物的降解很可能是导致pH值升高的原因。这些发现旨在补充负责解读此类临界无效pH值结果的医学审核官员所使用的信息。