Macchia Alejandro, Figar Silvana, Biscayart Cristián, González Bernaldo de Quirós Fernán
Subsecretaría de Planificación Sanitaria Ministerio de Salud de la Ciudad de Buenos Aires Ciudad Autónoma de Buenos Aires Argentina Subsecretaría de Planificación Sanitaria, Ministerio de Salud de la Ciudad de Buenos Aires, Ciudad Autónoma de Buenos Aires, Argentina.
Área de Investigación en Salud Poblacional de la Secretaría de Investigación de la Universidad Hospital Italiano de Buenos Aires Global Epidemiology-IMTIB-CONICET Argentina Área de Investigación en Salud Poblacional de la Secretaría de Investigación de la Universidad Hospital Italiano de Buenos Aires, Global Epidemiology-IMTIB-CONICET, Argentina.
Rev Panam Salud Publica. 2024 Dec 4;48:e129. doi: 10.26633/RPSP.2024.129. eCollection 2024.
This study evaluated the association between serologically confirmed prior dengue infection and the subsequent risk of virologically confirmed dengue, severe dengue, dengue hospitalization, dengue-related death and all-cause mortality.
A systematic review and meta-analysis were conducted following PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines. PubMed, CINAHL, MEDLINE, the Cochrane Library and Web of Science were searched for reports of phase III randomized controlled trials of vaccine efficacy that had data about the placebo group and information about prior infections and were published between January 1994 and March 2024. Random-effects models were used to calculate combined odds ratios (ORs), and heterogeneity was assessed.
Four studies from three phase III trials were included. Participants with prior infection had a lower likelihood of developing virologically confirmed dengue during follow up (OR: 0.85, 95% confidence interval [CI]: 0.75 to 0.98, = 0.024) and the same risk of dengue hospitalization as those without prior infection (OR: 1.18, 95% CI: 0.92 to 1.53, = 0.198). However, they had a higher rate of severe dengue (OR: 2.91, 95% CI: 1.23 to 6.87, = 0.015). No dengue-related deaths occurred during follow up. There were no statistically significant differences in all-cause mortality between individuals with and without prior dengue (OR: 1.74, 95% CI: 0.21 to 14.08, = 0.76).
Prior dengue infection significantly reduced the risk of virologically confirmed dengue and increased the risk of severe dengue, but had no significant effect on dengue hospitalization, dengue-related death or all-cause mortality during follow up. These findings suggest the need to reconsider prior infection as an independent risk factor.
本研究评估血清学确诊的既往登革热感染与后续病毒学确诊的登革热、重症登革热、登革热住院、登革热相关死亡及全因死亡率之间的关联。
按照PRISMA(系统评价和Meta分析的首选报告项目)指南进行系统评价和Meta分析。检索了PubMed、CINAHL、MEDLINE、Cochrane图书馆和Web of Science,以查找1994年1月至2024年3月期间发表的关于疫苗效力的III期随机对照试验报告,这些报告包含安慰剂组的数据以及既往感染的信息。采用随机效应模型计算合并比值比(OR),并评估异质性。
纳入了三项III期试验中的四项研究。既往感染的参与者在随访期间发生病毒学确诊登革热的可能性较低(OR:0.85,95%置信区间[CI]:0.75至0.98,P = 0.024),且登革热住院风险与未感染既往感染者相同(OR:1.18,95%CI:0.92至1.53,P = 0.198)。然而,他们的重症登革热发生率较高(OR:2.91,95%CI:1.23至6.87,P = 0.015)。随访期间未发生登革热相关死亡。既往有登革热和无登革热的个体在全因死亡率方面无统计学显著差异(OR:1.74,95%CI:0.21至14.08,P = 0.76)。
既往登革热感染显著降低了病毒学确诊登革热的风险并增加了重症登革热的风险,但对随访期间的登革热住院、登革热相关死亡或全因死亡率无显著影响。这些发现表明有必要重新考虑将既往感染作为一个独立的危险因素。