Evaluation of the NS1 Rapid Test and the WHO Dengue Classification Schemes for Use as Bedside Diagnosis of Acute Dengue Fever in Adults

被引:94
作者
Chaterji, Shera [1 ]
Allen, John Carson, Jr. [2 ]
Chow, Angelia [1 ]
Leo, Yee-Sin [3 ]
Ooi, Eng-Eong [1 ]
机构
[1] Duke NUS Grad Med Sch, Program Emerging Infect Dis, Singapore 169854, Singapore
[2] Duke NUS Grad Med Sch, Ctr Quantitat Med, Singapore 169854, Singapore
[3] Tan Tock Seng Hosp, Communicable Dis Ctr, Singapore, Singapore
基金
英国医学研究理事会;
关键词
INDIRECT IMMUNOFLUORESCENCE; MONOCLONAL-ANTIBODIES; PROTEIN NS1; VIRUS; INFECTION; ANTIGEN; ASSAY; SINGAPORE; TIME;
D O I
10.4269/ajtmh.2011.10-0316
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Because healthcare facilities in many dengue endemic countries lack laboratory support, early dengue diagnosis must rely on either clinical recognition or a bedside diagnostic test. We evaluated the sensitivity and specificity of the 1997 and 2009 World Health Organization (WHO) dengue classification schemes and the NS1 strip test in acute sera from 154 virologically confirmed dengue patients and 200 patients with other febrile illnesses. Both WHO classification schemes had high sensitivity but lacked specificity. The NS1 strip test had high specificity, but its sensitivity was significantly lower in secondary compared with primary dengue infections. Differences in viral serotypes did not affect the performance of any of the three diagnostic approaches. Taken collectively, our findings indicate that the 1997 WHO dengue case definition can be used to exclude dengue, and the NS1 strip test can be used to confirm dengue infection, although the latter should be interpreted with caution in regions where secondary dengue infection is prevalent.
引用
收藏
页码:224 / 228
页数:5
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