RESEARCH ARTICLE |
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Year : 2014 | Volume
: 51
| Issue : 3 | Page : 153-164 |
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On the risk of severe dengue during secondary infection: A systematic review coupled with mathematical modeling
Kenji Mizumoto1, Keisuke Ejima2, Taro Yamamoto3, Hiroshi Nishiura2
1 Graduate School of Arts and Sciences; Graduate School of Medicine, The University of Tokyo, Tokyo, Japan 2 Graduate School of Medicine, The University of Tokyo, Tokyo, Japan 3 Department of International Health, Nagasaki University Institute of Tropical Medicine and GCOE, Sakamoto, Nagasaki, Japan
Correspondence Address:
Hiroshi Nishiura Graduate School of Medicine, The University of Tokyo, Medical Building No. 3, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033 Japan
 Source of Support: None, Conflict of Interest: None  | Check |
PMID: 25253207 
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Background & objectives: The present study aimed to systematically quantify the well known risk of severe dengue during secondary infection in literature and to understand how epidemiological mechanisms of enhancement during the secondary infection influence the empirically estimated risk of severe dengue by means of mathematical modeling.
Methods: Two conditional risks of severe dengue, i.e. symptomatic illness and dengue hemorrhagic fever (DHF) or dengue shock syndrome (DSS), given secondary infection were explored based on systematically searched prospective studies. A two-strain epidemiological model was employed to simulate the transmission dynamics of dengue and to identify the relevant data gaps in empirical observations.
Results: Using the variance-based weighting, the pooled relative risk (RR) of symptomatic illness during secondary infection was estimated at 9.4 [95% confidence interval (CI): 6.1-14.4], and similarly, RR of DHF/DSS was estimated to be 23.7 (95% CI: 15.3-36.9). A variation in the RR of DHF/DSS was observed among prospective studies. Using the mathematical modeling technique, we identified the duration of cross-protective immunity as an important modulator of the time-dependent behaviour of the RR of severe dengue. Different epidemiological mechanisms of enhancement during secondary infection yielded different RR of severe dengue.
Interpretation & conclusion: Optimal design of prospective cohort study for dengue should be considered, accounting for the time-dependence in the RR during the course of dengue epidemic. It is critical to statistically infer the duration of cross-protective immunity and clarify how the enhancement influences the epidemiological dynamics during secondary infection. |
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