Reactive and pre-emptive vaccination strategies to control hepatitis E infection in emergency and refugee settings: A modelling study.
Reactive and pre-emptive vaccination strategies to control hepatitis E infection in emergency and refugee settings: A modelling study.
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DOI:
10.1371/journal.pntd.0006807
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发表时间:
2018-09
影响因子:
3.8
通讯作者:
Siddiqui R
中科院分区:
文献类型:
--
作者:
Cooper BS;White LJ;Siddiqui R
Hepatitis E Virus (HEV) is the leading cause of acute viral hepatitis globally. Symptomatic infection is associated with case fatality rates of ~20% in pregnant women and it is estimated to account for ~10,000 annual pregnancy-related deaths in southern Asia alone. Recently, large and well-documented outbreaks with high mortality have occurred in displaced population camps in Sudan, Uganda and South Sudan. However, the epidemiology of HEV is poorly defined, and the value of different immunisation strategies in outbreak settings uncertain. We aimed to estimate the critical epidemiological parameters for HEV and to evaluate the potential impact of both reactive vaccination (initiated in response to an epidemic) and pre-emptive vaccination. We analysed data from one of the world's largest recorded HEV epidemics, which occurred in internally-displaced persons camps in Uganda (2007–2009), using transmission dynamic models to estimate epidemiological parameters and assess the potential impact of reactive and pre-emptive vaccination strategies. Under baseline assumptions we estimated the basic reproduction number of HEV in three separate camps to range from 3.7 (95% Credible Interval [CrI] 2.8, 5.1) to 8.5 (5.3, 11.4). Mean latent and infectious periods were estimated to be 34 (95% CrI 28, 39) and 40 (95% CrI 23, 71) days respectively. Assuming 90% vaccine coverage, reactive two-dose vaccination of those aged 16–65 years excluding pregnant women (for whom vaccine is not licensed), if initiated after 50 reported cases, led to mean camp-specific reductions in mortality of 10 to 29%. Pre-emptive vaccination with two doses reduced mortality by 35 to 65%. Both strategies were more effective if coverage was extended to groups for whom the vaccine is not currently licensed. For example, two dose pre-emptive vaccination, if extended to include pregnant women, led to mean reductions in mortality of 66 to 82%. HEV has a high transmission potential in displaced population settings. Substantial reductions in mortality through vaccination are expected, even if used reactively. There is potential for greater impact if vaccine safety and effectiveness can be established in pregnant women. Hepatitis E virus is a leading cause of acute viral hepatitis in developing countries. About 20% of those infected develop clinical symptoms; of those, about 2% of non-pregnant cases and 20% of pregnant cases die. There is a safe and effective HEV vaccine that is licensed in China for those aged 16–65 years who are not pregnant. The potential for using this vaccine in outbreak settings has not previously been examined. We analysed data from one of the world’s largest recorded HEV epidemics. We estimated that one case infects, on average, between 4 and 9 others at the start of an epidemic. We found that vaccination restricted to those aged 16–65 who are not pregnant could reduce mortality in outbreak settings by between about 10 and 30% if used reactively (initiating vaccination after the start of an epidemic); pre-emptive vaccination of the same group could reduce mortality by 35–65%. Substantially higher reductions in mortality are likely if vaccination can be safely extended to pregnant women and other age groups without loss of effectiveness. However, even if this is possible, reactive vaccination is unlikely to reduce mortality by more than 50% while pre-emptive vaccination can reduce mortality by 80 to 100%.
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影响因子:
3.7
作者:
Amanya G;Kizito S;Nabukenya I;Kalyango J;Atuheire C;Nansumba H;Abwoye SA;Opio DN;Kibuuka E;Karamagi C
通讯作者:
Karamagi C
DOI:
10.1097/ede.0b013e3182572581
发表时间:
2012-07
期刊:
Epidemiology (Cambridge, Mass.)
影响因子:
--
作者:
Grad YH;Miller JC;Lipsitch M
通讯作者:
Lipsitch M
影响因子:
4.8
作者:
Chandra NS;Sharma A;Malhotra B;Rai RR
通讯作者:
Rai RR
影响因子:
11.8
作者:
Boccia, Delia;Guthmann, Jean-Paul;Guerin, Philippe Jean
通讯作者:
Guerin, Philippe Jean
影响因子:
3.7
作者:
Nannyonga, Betty;Sumpter, David J. T.;Luboobi, Livingstone S.
通讯作者:
Luboobi, Livingstone S.