Falconar Andrew K I, Romero-Vivas Claudia M E
Laboratorio de Enfermedades Tropicales, Departamento de Medicina, Fundacion Universidad del Norte Km5 Antigua Via a Puerto Colombia, Barranquilla, Colombia, South America.
J Clin Med Res. 2012 Feb;4(1):33-44. doi: 10.4021/jocmr694w. Epub 2012 Jan 17.
SEVERE DENGUE DISEASE (SDD) (DHF/DSS: dengue hemorrhagic fever/dengue shock syndrome) results from either primary or secondary dengue virus (DENV) infections, which occur 4 - 6 days after the onset of fever. As yet, there are no definitive clinical or hematological criteria that can specifically identify SDD patients during the early acute febrile-phase of disease (day 0 - 3: < 72 hours). This study was performed during a SDD (DHF/DSS) epidemic to: 1) identify the DENV serotypes that caused SDD during primary or secondary DENV infections; 2) identify simple clinical and hematological criteria that could significantly discriminate between patients who subsequently developed SDD versus non-SDD (N-SDD), or had a non-DENV fever of unknown origin (FUO) during day 0 - 3 of fever; 3) assess whether DENV serotype co-infections resulted in SDD.
First serum samples, with clinical and hematological criteria, were collected from 100 patients during the early acute febrile-phase (day 0 - 3: < 72 hours), assessed for DENV or FUO infections by IgM- and IgG-capture ELISAs on paired serum samples and by DENV isolations, and subsequently graded as SDD, N-SDD or FUO patients.
IN THIS STUDY: 1) Thirty-three patients had DENV infections, predominantly secondary DENV-2 infections, including each SDD (DHF/DSS) case; 2) Secondary DENV-2/-3 and DENV-2/-4 serotype co-infections however resulted in N-SDD; 3) Each patient who subsequently developed SDD, but none of the others, displayed three clinical criteria: abdominal pain, conjunctival injection and veni-puncture bleeding, therefore each of these criteria provided definitively significant prognostic (P < 0.001) values; 4) Petechia, positive tourniquet tests and hepatomegaly, and neutrophilia or leukopenia also significantly identified those who: a) subsequently developed SDD versus N-SDD, or had a FUO; b) subsequently developed SDD versus N-SDD; c) subsequently developed N-SDD versus FUOs, respectively.
This is the first report of simple definitively prognostic criteria for SDD patients, including the first assessment and confirmation of conjunctival injection. The three definitive clinical criteria used alone, or supported by the other four criteria, could be essential for specifically identifying those patients needing prompt hospital-based therapies to lessen or avert SDD, without unnecessary hospitalization of the other patients.
Dengue virus; Severe dengue; Dengue fever; Diagnostic; Criteria; Hemorrhage; Shock.
严重登革热疾病(SDD)(登革出血热/登革休克综合征:DHF/DSS)由原发性或继发性登革病毒(DENV)感染引起,这些感染发生在发热开始后的4 - 6天。迄今为止,尚无明确的临床或血液学标准能够在疾病的早期急性发热期(第0 - 3天:< 72小时)特异性识别SDD患者。本研究在一次SDD(DHF/DSS)流行期间进行,目的是:1)确定在原发性或继发性DENV感染期间导致SDD的DENV血清型;2)确定能够显著区分随后发展为SDD与非SDD(N - SDD)患者,或在发热第0 - 3天患有不明原因非DENV发热(FUO)患者的简单临床和血液学标准;3)评估DENV血清型合并感染是否导致SDD。
在早期急性发热期(第0 - 3天:< 72小时)从100例患者中采集首次血清样本,并记录临床和血液学标准,通过对配对血清样本进行IgM和IgG捕获ELISA以及DENV分离来评估DENV或FUO感染情况,随后将患者分为SDD、N - SDD或FUO患者。
在本研究中:1)33例患者感染了DENV,主要是继发性DENV - 2感染,包括每例SDD(DHF/DSS)病例;2)然而,继发性DENV - 2/-3和DENV - 2/-4血清型合并感染导致N - SDD;3)每例随后发展为SDD的患者,但其他患者均未出现,表现出三个临床标准:腹痛、结膜充血和静脉穿刺出血,因此这些标准中的每一个都具有明确的显著预后价值(P < 0.001);4)瘀点、束臂试验阳性和肝肿大,以及中性粒细胞增多或白细胞减少也显著识别出以下患者:a)随后发展为SDD与N - SDD患者,或患有FUO的患者;b)随后发展为SDD与N - SDD患者;c)随后发展为N - SDD与FUO患者。
这是关于SDD患者简单明确预后标准的首次报告,包括对结膜充血的首次评估和确认。单独使用这三个明确的临床标准或由其他四个标准支持,对于特异性识别那些需要及时住院治疗以减轻或避免SDD的患者至关重要,同时避免其他患者不必要的住院。
登革病毒;严重登革热;登革热;诊断;标准;出血;休克