Provincial Laboratory for Public Health, Edmonton, Alberta, Canada.
J Clin Microbiol. 2013 Jun;51(6):1850-4. doi: 10.1128/JCM.00195-13. Epub 2013 Apr 3.
In clinical laboratories, diagnosis of imported malaria is commonly performed by microscopy. However, the volume of specimens is generally low and maintaining proficiency in reading blood smears, particularly at the species level, is challenging in this setting. To address this problem, the Provincial Laboratory for Public Health (ProvLab) in Alberta, Canada, implemented real-time PCR for routine confirmation of all smear-positive samples in the province. Here we report our experience over a 4-year period (2008 to 2012) with this new diagnostic algorithm. While detection of Plasmodium falciparum by microscopy alone was accurate, real-time PCR served as an important adjunct to microscopy for the identification of non-falciparum species. In 18% of cases, the result was reported as non-falciparum or the species could not be identified by microscopy alone, and in all cases, the species was resolved by real-time PCR. In another 4% of cases, the species was misidentified by microscopy. To enhance surveillance for malaria, we integrated our demographic, clinical, and laboratory data into a new system developed by the Canadian Network for Public Health Intelligence, called the Malaria System for Online Surveillance (SOS). Using this application, we characterized our patient populations and travel history to identify risk factors associated with malaria infection abroad.
在临床实验室中,通常通过显微镜检查来诊断输入性疟疾。然而,标本量通常较少,在这种情况下,要保持阅读血涂片的熟练度,特别是在物种水平上,具有挑战性。为了解决这个问题,加拿大艾伯塔省的省级公共卫生实验室(ProvLab)实施了实时聚合酶链反应(PCR),以常规确认该省所有涂片阳性的样本。在此,我们报告了在 4 年期间(2008 年至 2012 年)使用这种新诊断算法的经验。虽然仅通过显微镜检查就能准确检测出恶性疟原虫,但实时 PCR 可作为显微镜检查的重要辅助手段,用于鉴定非恶性疟原虫物种。在 18%的病例中,结果报告为非恶性疟原虫或单独通过显微镜检查无法识别物种,在所有情况下,均可通过实时 PCR 确定物种。在另外 4%的病例中,显微镜检查错误地鉴定了物种。为了加强疟疾监测,我们将我们的人口统计学、临床和实验室数据整合到一个由加拿大公共卫生情报网络开发的新系统中,称为在线监测疟疾系统(SOS)。使用该应用程序,我们描述了我们的患者人群和旅行史,以确定与国外疟疾感染相关的风险因素。