Thanachartwet Vipa, Wattanathum Anan, Oer-areemitr Nittha, Jittmittraphap Akanitt, Sahassananda Duangjai, Monpassorn Chalida, Surabotsophon Manoon, Desakorn Varunee
Department of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, 10400, Thailand.
Pulmonary and Critical Care Division, Department of Medicine, Phramongkutklao Hospital, 315 Rajvithi Road, Ratchathewi District, Bangkok, 10400, Thailand.
BMC Infect Dis. 2016 Feb 1;16:46. doi: 10.1186/s12879-016-1386-5.
Dengue is the most common mosquito-borne viral disease in humans. However, the sensitivities of warning signs (WSs) for identifying severe dengue in adults are low, and the utility of lactate levels for identifying severe dengue in adults has not been verified. Therefore, we aimed to evaluate the diagnostic accuracy of using peripheral venous lactate levels (PVL), as well as WSs established by the World Health Organization, for identifying severe dengue.
We prospectively evaluated individuals hospitalized for dengue who were admitted to the Hospital for Tropical Diseases in Thailand between May 2013 and January 2015. Blood samples to evaluate PVL levels were collected at admission and every 24 h until the patient exhibited a body temperature of <37.8 °C for at least 24 h. Data were recorded on a pre-defined case report form, including baseline characteristics, clinical parameters, and laboratory findings.
Among 125 patients with confirmed dengue, 105 (84.0%) patients had non-severe dengue, and 20 (16.0%) patients had severe dengue. The presence of clinical fluid accumulation as a WS provided high sensitivity (75.0%, 95% confidence interval [CI]: 50.9-91.3%) and specificity (90.5%, 95% CI: 83.2-95.3%). The PVL level at admission was used to evaluate its diagnostic value, and receiver operating characteristic curve analysis revealed an area under the curve of 0.84 for identifying severe dengue. At the optimal cutoff value (PVL: 2.5 mmol/L), the sensitivity and specificity were 65.0% (95% CI: 40.8-84.6%) and 96.2% (95% CI: 90.5-99.0%), respectively. A combined biomarker comprising clinical fluid accumulation and/or PVL of ≥2.5 mmol/L provided the maximum diagnostic accuracy for identifying severe dengue, with a sensitivity of 90.0% (95% CI: 68.3-98.8%) and a specificity of 87.6% (95% CI: 79.8-93.2%).
Clinical fluid accumulation and/or PVL may be used as a diagnostic biomarker of severe dengue among adults. This biomarker may facilitate early recognition and timely treatment of patients with severe dengue, which may reduce dengue-related mortality and hospital burden.
登革热是人类最常见的蚊媒病毒性疾病。然而,用于识别成人重症登革热的警示体征(WSs)的敏感性较低,且乳酸水平用于识别成人重症登革热的效用尚未得到验证。因此,我们旨在评估使用外周静脉乳酸水平(PVL)以及世界卫生组织制定的警示体征来识别重症登革热的诊断准确性。
我们前瞻性评估了2013年5月至2015年1月期间入住泰国热带病医院的登革热住院患者。入院时及之后每24小时采集血样以评估PVL水平,直至患者体温<37.8°C至少持续24小时。数据记录在预先定义的病例报告表上,包括基线特征、临床参数和实验室检查结果。
在125例确诊登革热患者中,105例(84.0%)为非重症登革热,20例(16.0%)为重症登革热。作为一种警示体征的临床液体潴留具有较高的敏感性(75.0%,95%置信区间[CI]:50.9 - 91.3%)和特异性(90.5%,95%CI:83.2 - 95.3%)。入院时的PVL水平用于评估其诊断价值,受试者工作特征曲线分析显示识别重症登革热的曲线下面积为0.84。在最佳截断值(PVL:2.5 mmol/L)时,敏感性和特异性分别为65.0%(95%CI:40.8 - 84.6%)和96.2%(95%CI:90.5 - 99.0%)。一种包含临床液体潴留和/或PVL≥2.5 mmol/L的联合生物标志物在识别重症登革热方面具有最高的诊断准确性,敏感性为90.0%(95%CI:68.3 - 98.8%),特异性为87.6%(95%CI:79.8 - 93.2%)。
临床液体潴留和/或PVL可作为成人重症登革热的诊断生物标志物。这种生物标志物可能有助于早期识别和及时治疗重症登革热患者,这可能降低登革热相关的死亡率和医院负担。