Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Microbiology Laboratory, Mahosot Hospital, Vientiane, Lao People's Democratic Republic.
J Clin Microbiol. 2013 Jan;51(1):142-8. doi: 10.1128/JCM.02360-12. Epub 2012 Oct 24.
In most areas where typhoid is endemic, laboratory diagnosis is not possible due to the lack of appropriate facilities. We investigated whether the combination of blood culture amplification of Salmonella enterica serovar Typhi with an S. Typhi antigen rapid diagnostic test (RDT) could be an accurate and inexpensive tool for the accelerated diagnosis of patients with acute typhoid in Laos. For a panel of 23 Gram-negative reference pathogens, the Standard Diagnostics (catalog no. 15FK20; Kyonggi-do, South Korea) RDT gave positive results for S. Typhi NCTC 8385, S. Typhi NCTC 786 (Vi negative), Salmonella enterica serovar Enteritidis (ATCC 13076), and Salmonella enterica serovar Ndolo NCTC 8700 (all group D). In a prospective study of 6,456 blood culture bottles from 3,028 patients over 15 months, 392 blood culture bottles (6.1%) from 221 (7.3%) patients had Gram-negative rods (GNRs) seen in the blood culture fluid. The sensitivity, negative predictive value, specificity, and positive predictive value were 96.7%, 99.5%, 97.9%, and 87.9%, respectively, for patients with proven S. Typhi bacteremia and 91.2%, 98.4%, 98.9%, and 93.9% for patients with group D Salmonella. The median (range) number of days between diagnosis by RDT and reference assays was 1 (-1 to +2) day for those with confirmed S. Typhi. The use of antigen-based pathogen detection in blood culture fluid may be a useful, relatively rapid, inexpensive, and accurate technique for the identification of important causes of bacteremia in the tropics.
在伤寒流行的大多数地区,由于缺乏适当的设施,无法进行实验室诊断。我们研究了伤寒沙门氏菌血培养扩增与伤寒沙门氏菌抗原快速诊断检测(RDT)的组合是否可以成为加速诊断老挝急性伤寒患者的准确且廉价的工具。对于一组 23 种革兰氏阴性参考病原体,Standard Diagnostics(目录号 15FK20;京畿道,韩国)RDT 对伤寒沙门氏菌 NCTC 8385、伤寒沙门氏菌 NCTC 786(Vi 阴性)、肠炎沙门氏菌(ATCC 13076)和肠炎沙门氏菌 Ndolo NCTC 8700(所有 D 组)呈阳性结果。在对 15 个月内来自 3028 名患者的 6456 个血培养瓶进行的前瞻性研究中,来自 221 名(7.3%)患者的 392 个血培养瓶(6.1%)在血培养物中观察到革兰氏阴性杆菌(GNRs)。对于证实有伤寒沙门氏菌菌血症的患者,灵敏度、阴性预测值、特异性和阳性预测值分别为 96.7%、99.5%、97.9%和 87.9%,对于 D 组沙门氏菌患者分别为 91.2%、98.4%、98.9%和 93.9%。通过 RDT 和参考检测确诊的患者,从诊断到确诊的中位数(范围)天数为 1 天(-1 至+2)。在热带地区,使用基于抗原的病原体检测血培养物可能是一种有用的、相对快速的、廉价的、准确的技术,可以鉴定引起菌血症的重要病原体。