Ko J-H, Peck K R, Lee W J, Lee J Y, Cho S Y, Ha Y E, Kang C-I, Chung D R, Jung C W, Kang E-S, Song J-H
Division of Infectious Diseases, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul, 135-710, Republic of Korea.
Eur J Clin Microbiol Infect Dis. 2015 Jul;34(7):1437-41. doi: 10.1007/s10096-015-2370-5. Epub 2015 Apr 17.
Recent products of piperacillin/tazobactam (PTZ) from the original manufacturer, previously considered a major cause of galactomannan (GM) false-positivity, are reported not to be related to it. However, data regarding generic PTZ are limited and controversial. To evaluate the effect of generic PTZ on GM false-positivity in Korea, we performed a case-control study in adult patients with cancer. A case-control study was designed. Electronic medical records of cancer patients who were admitted and tested for serum GM between March and June 2014 at a tertiary care university hospital were reviewed. During the study period, a single generic PTZ (C manufacturer, Korea) was used. Patients who received PTZ within 24 h prior to serum GM testing were enrolled. Age- and GM test date-matched non-PTZ patients were selected as controls. A total of 110 patients received PTZ within 24 h prior to serum GM testing during the study period. The GM optical density index (ODI) of the PTZ group did not vary significantly from that of the control group (p = 0.251). The percentage of false-positive patients in the PTZ group was also similar to that of the control group (p = 0.538). There was no statistical relationship between GM ODI titer and time interval from PTZ administration (p = 0.095) or cumulative PTZ dose (p = 0.416). In a case-control study that evaluated 220 patients, a generic PTZ in Korea was not related to GM false-positivity.
哌拉西林/他唑巴坦(PTZ)原制造商近期生产的产品,此前被认为是半乳甘露聚糖(GM)假阳性的主要原因,但据报道与之无关。然而,关于通用型PTZ的数据有限且存在争议。为评估通用型PTZ对韩国GM假阳性的影响,我们对成年癌症患者进行了一项病例对照研究。设计了一项病例对照研究。回顾了2014年3月至6月在一家三级大学医院住院并接受血清GM检测的癌症患者的电子病历。在研究期间,使用了单一的通用型PTZ(韩国C制造商)。纳入在血清GM检测前24小时内接受PTZ治疗的患者。选择年龄和GM检测日期匹配的未接受PTZ治疗的患者作为对照。在研究期间,共有110名患者在血清GM检测前24小时内接受了PTZ治疗。PTZ组的GM光密度指数(ODI)与对照组相比无显著差异(p = 0.251)。PTZ组假阳性患者的百分比也与对照组相似(p = 0.538)。GM ODI滴度与PTZ给药后的时间间隔(p = 0.095)或PTZ累积剂量(p = 0.416)之间无统计学关系。在一项评估220名患者的病例对照研究中,韩国的一种通用型PTZ与GM假阳性无关。