Hostname: page-component-8448b6f56d-c4f8m Total loading time: 0 Render date: 2024-04-24T04:35:58.815Z Has data issue: false hasContentIssue false

Measles epidemic in Southern Vietnam: an age-stratified spatio-temporal model for infectious disease counts

Published online by Cambridge University Press:  12 September 2022

Thi Huyen Trang Nguyen*
Affiliation:
Hasselt University, Hasselt, Belgium The Pasteur Institute, Ho Chi Minh City, Vietnam
Christel Faes
Affiliation:
Hasselt University, Hasselt, Belgium
Niel Hens
Affiliation:
Hasselt University, Hasselt, Belgium The University of Antwerp, Antwerp, Belgium
*
Author for correspondence: Thi Huyen Trang Nguyen, E-mail: thihuyentrang.nguyen@uhasselt.be
Rights & Permissions [Opens in a new window]

Abstract

Measles resurged in Vietnam between 2018 and 2020, especially in the Southern region. The proportion of children with measles infection showed quite some variation at the provincial level. We applied a spatio-temporal endemic–epidemic modelling framework for age-stratified infectious disease counts using measles surveillance data collected in Southern Vietnam between 1 January 2018 and 30 June 2020. We found that disease transmission within age groups was greatest in young children aged 0–4 years whereas a relatively high between-group transmission was observed in older age groups (5–14 years, 15–24 years and 25+ years groups). At the provincial level, spatial transmission followed an age-dependent distance decay with measles spread mainly depending on local and neighbouring transmission. Our study helped to clarify the measles transmission dynamics in a more detailed fashion with respect to age strata, time and space. Findings from this study may help determine proper strategies in measles outbreak control including promotion of age-targeted intervention programmes in specific areas.

Type
Original Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
Copyright © The Author(s), 2022. Published by Cambridge University Press

Introduction

Measles is one of the most contagious viral diseases. The global reduction of measles incidence during 2000–2016 is a victory of intensive public health efforts, especially in surveillance and measles immunisation activities. There are no animal reservoirs and infections do not result in persistent shedding of the pathogen. Thus, measles transmission can only be sustained and outbreaks can only occur when the susceptible population has attained sufficient size [Reference Gay1]. Between 2016 and 2019, the world experienced a resurgence of measles, with an increase of 556% in the reported incidence observed globally, challenging the feasibility of the disease elimination goal [Reference Patel2]. This is largely due to the replenishment of individuals who are not immunised over successive birth cohorts [Reference Trentini3]. In other words, failure in maintaining high levels of measles immunity via vaccination eventually results in an accumulation of susceptibility in the population and an introduction of the virus could facilitate widespread transmission. Although effective vaccination programmes would reduce the supply of susceptible individuals into the population, spatial heterogeneity of the vaccination coverage has been associated with the occurrence of local outbreaks [Reference Glasser4, Reference Herzog, Paul and Held5]. The circulation of measles virus is also correlated with other stochastic local determinants such as population density, inter-regional human movement [Reference Qin6, Reference Parpia7] and mixing behaviour [Reference Wallinga, Teunis and Kretzschmar8Reference Bansal, Grenfell and Meyers10]. For example, short-term migration of susceptible populations (e.g. rural-to-urban) may increase the input of susceptibilities in metropolitan areas, and thus exacerbate the risk of outbreaks in these localities [Reference Qin6, Reference Parpia7]. Furthermore, as contact patterns of age-assortative mixing are usually observed [Reference Horby11, Reference Mossong12], the risk of measles infection is greater when individuals in under-immunised communities preferentially cluster in their age class [Reference Funk13, Reference Hens14].

In Vietnam, the vaccine schedule is a two-dose schedule that the first and second doses of measles containing vaccine (MCV1 and MCV2) are given at 9 and 18 months old, respectively. Despite the high coverage over the last decade (>95% for MCV1 and >80% for MCV2 [15]), sustained epidemics of measles occurred during 2018–2020. The Southern region, which consists of 20 provincial units (the province of Lam Dong, five provinces and a city in the South East region, 12 provinces and a city in the Mekong River Delta region), was heavily affected with more than 26 000 cases reported in total. Heterogeneous distribution of measles incidence in different age groups in relation to space and time was observed in the reported case data. This raised the interest to investigate the spreading patterns of measles in Southern Vietnam and the degree to which these transmission patterns are influenced by age and geographical areas. We fitted an age-structured spatio-temporal statistical model for infectious disease counts [Reference Held, Höhle and Hofmann16, Reference Meyer and Held17] in which the number of infections is additively decomposed into an endemic and epidemic component. While the latter component describes the occasional outbreaks that are linked to previous cases within- or between-geographical units, the endemic part captures exogenous factors that explain incidence not directly linked to past counts. To simultaneously investigate the transmission across age groups, we accounted for the age-structured mixing pattern, which was adapted from a social contact study in Vietnam in 2007 [Reference Horby11]. We used routine surveillance data for daily reported counts of measles collected between 1 January 2018 and 30 June 2020 stratified by age group and by provincial unit in the South of Vietnam. Results from this study can provide more insights into the measles outbreak dynamics and more effectively inform age-targeted containment measures in the country (e.g. age-targeted vaccination campaigns, health communications).

Method

Measles surveillance data

In Vietnam, measles is one of the 20 infectious diseases that are required to be notified online to the Electronic Communicable Disease Surveillance System (ECDS) within 24 h post clinical diagnosis. In the case report form, several fields including demographic characteristics, date of illness onset, date of hospitalisation or medical examination of in- and out-patients are obligated to be reported. More information about the disease surveillance and reporting system in Vietnam can be found in [18, 19]. In this study, we analysed measles cases reported between 1 January 2018 and 30 June 2020 in the Southern region. On 11 October 2020, 26 047 individual cases were extracted from the ECDS, accessed by the Pasteur Institute in Ho Chi Minh City, the public health institute that manages the disease surveillance system in the South. For the age-structured spatio-temporal analysis of the outbreak, we categorised individuals into four age groups: 0–4 (children), 5–14 (school children), 15–24 (adolescent and young adults) and 25+ (adults) years of age. Overall, the median age at disease onset was 3 years, ranging from <1 year to 84 years. The most affected age group was 0–4 years, which accounted for 61.4% of measles cases while the 5–14 years, 15–24 years and 25+ years groups represented 22.0%, 4.5% and 12.1% of the total cases, respectively. Based on the date of onset, we aggregated the daily number of cases by age group in each province in which the cases resided. Figure 1 depicts the evolution of daily counts of measles infections and monthly incidence per 100 000 population by age group and Figure 2 presents maps of the age-specific cumulative incidence per 100 000 individuals across all provinces.

Fig. 1. Evolution of age-specific measles cases by date of symptom onset (left axes) and incidence per 100 000 population by month (blue lines, right axes) in Southern Vietnam, 1 January 2018 to 30 June 2020. Lunar New Year in 2019 and 2020 are highlighted in red.

Fig. 2. Maps of age-specific cumulative incidence per 100 000 population in Southern Vietnam, 1 January 2018 to 30 June 2020.

Population data

Age- and province-specific population data were obtained from the census data in 2019 [20]. The Southern population was approximately 36 million in 2019, and in each age group, the population fraction was 6.7% for 0–4 years, 14.9% for 5–14 years, 14.3% for 15–24 years and 64.2% for 25+ years. We assumed that the total population was constant over the period 2018–2020.

Social contact data

To reflect the amount of mixing between age groups, we used social contact data, adapted from an empirical contact matrix in a survey in the Red River Delta region of Northern Vietnam in 2007 [Reference Horby11]. The matrix was transformed because of the difference in demographic structures between Northern and Southern Vietnam and hence, directly using the original contact matrix would not be valid in our study. First, we extracted the social contact patterns aggregated to the age groups of interest from the Social Contact Rates (SOCRATES) Data Tool (http://www.socialcontactdata.org/socrates/) [Reference Willem21]. This age-structured contact matrix ${\boldsymbol C} = ( {{\boldsymbol c}_{{g}^{\prime}g}} )$ provided the average non-negative number of contacts of a person in age group g (rows) with a contact in age group g (columns) in 1 day (Fig. 3a) aggregated over weekdays or weekends, contact duration, physical or non-physical contacts and gender. Next, we projected the social contact matrix for Southern Vietnam ${\boldsymbol C}_{( {\boldsymbol P} ) } = ( {{\boldsymbol c}_{( {\boldsymbol P} ) {g}^{\prime}g}} )$ using the density correction method proposed by Arregui et al. [Reference Arregui22]. The projected contact matrix is a product of an intrinsic connectivity matrix C(N/N g) and the fraction of individuals in the age group of the contact $N_g^{\prime} /{N}^{\prime}$, where N g and $N_g^{\prime}$ are the demographic structures in 2009 (Red River Delta region) and 2019 (Southern region), respectively. Note that because the age-structured population numbers of Red River Delta region are not available for 2007, we used population of Red River Delta region from the 2009 census [20]. The obtained contact matrix is shown in Figure 3b.

Fig. 3. (a) Original age-structured contact matrix C estimated in Northern Vietnam anno 2007 aggregated to the age groups of interest and (b) the age-structured contact matrix projected for Southern Vietnam C(P) based on (a). The entries contain the mean number of contacts made by one participant per day. (c), (d), (e) and (f) refer to the power transformation of row-normalised contact matrix C(P) for different values of κ.

Age-structured spatio-temporal analysis

In general, we leveraged an endemic–epidemic modelling framework for multivariate infectious disease counts first introduced by Held et al. [Reference Held, Höhle and Hofmann16] and extended in a series of publications [Reference Herzog, Paul and Held5, Reference Meyer and Held17, Reference Paul and Held23Reference Held, Meyer and Bracher26, Reference Geilhufe38, Reference Bracher and Held39]. The framework subsequently incorporated the age-structured contact matrix (possibly adjusted) to better understand disease spread in the scenario of heterogeneous mixing [Reference Meyer and Held17].

Formally, let Y grt denote the number of cases in age group g = 1, …, G in province r = 1, …, R at time t = 1, …, T. Conditional on the number of cases at the previous time point t − 1, the counts are assumed to follow a negative binomial distribution with conditional mean μ grt:

(1)$$\mu _{grt} = e_{gr}\nu _{grt} + \phi _{grt}\mathop \sum \limits_{{g}^{\prime}, r^{\prime}} \lfloor{{\boldsymbol c}_{( {\boldsymbol P} ) g^{\prime}g}{\cal W}_{{r}^{\prime}r}\;} \rfloor Y_{{g}^{\prime}, {r}^{\prime}, t-1}$$

and a variance μ grt(1 + μ grtψ g) with a group-specific overdispersion parameter ψ g > 0 [Reference Meyer and Held17, Reference Held, Meyer and Bracher26]. Note that if ψ g = 0, the distribution simplifies to the Poisson distribution. The mean μ grt is decomposed into endemic and epidemic components. The former component exhibits baseline patterns. The latter component involves an autoregressive effect that links cases at time point t in unit r with observations at the previous time point t − 1 and in units r  = 1, …, R. Specifically, the non-negative parameters ν grt and ϕ grt are modelled as log-linear predictors:

(2)$$\log ( {\nu_{grt}} ) = \alpha _g^{( \nu ) } + \alpha _{mekong}^{( \nu ) } + \beta _{lunar}^{( \nu ) } x_t + \beta _{trend}^{( \nu ) } t + \beta _{{\rm sin}}\sin ( {\omega t} ) + \beta _{{\rm cos}}{\rm cos}( {\omega t} ) $$
(3)$$\log ( {\phi_{grt}} ) = \alpha _g^{( \phi ) } + \alpha _r^{( \phi ) } + \beta _{lunar}^{( \phi ) } x_t + {\rm \tau }\log ( {e_{gr}} ) .$$

The above two equations contain age-specific fixed effects ($\alpha _g^{( \nu ) }$, $\alpha _g^{( \phi ) }$). Because we deemed that fewer cases were reported during the Lunar New Year, we included an indicator for the holiday in 2019 and 2020 with coefficient β lunar (x t = 1 for dates from 2 to 10 February 2019 and from 23 to 29 January 2020, otherwise x t = 0). In the endemic component, to adjust for the possibly different number of individuals at risk in each province and age group, we included the population size e gr as an offset [Reference Meyer and Held25]. To allow for the differences amongst the two main administrative regions, $\alpha _{mekong}^{( \nu ) }$ is included to resemble the effect of the Mekong River Delta region. We also assumed that the disease incidence varies with a linear time effect (β trend) and an overall seasonal sine–cosine term where the sinusoidal wave of frequency ω identified as 2π/365 for daily continuous measurement [Reference Held and Paul24]. In the epidemic component, we allowed for province-specific effects $\alpha _r^{( \phi ) }$ and accounted for population size e gr to quantify how ‘attraction’ to a province r scales with population size in group g, in which the strength of population scaling factor τ is to be estimated [Reference Meyer and Held25, Reference Xia, Bjørnstad and Grenfell27].

To determine transmission weights from age stratum g to age stratum g (i.e. ${\boldsymbol c}_{( {\boldsymbol P} ) g^{\prime}g}$), and from area r to r (i.e. ${\cal W}_{{r}^{\prime}r}$), the product ${\boldsymbol c}_{( {\boldsymbol P} ) g^{\prime}g}{\cal W}_{{r}^{\prime}r}$, which is row-normalised, i.e. $\sum\nolimits_{g, r} {\lfloor{{\boldsymbol c}_{( {\boldsymbol P} ) g^{\prime}g}{\cal W}_{{r}^{\prime}r}} \rfloor } = 1$ was introduced in the epidemic component. In ideal circumstances, to best reflect the transmission between strata, the matrices of contact and mobility should be displayed by age and province. Nevertheless, such data sources are not easily available as collecting contact and movement patterns is cumbersome. In our study, we took the overall estimate of contact data for age-group weights and used the power law approximation for the spatial weights. First, the age-group weights ${\boldsymbol c}_{( {\boldsymbol P} ) g^{\prime}g}$ are row-normalised and then raise it to the power κ ≥ 0, i.e. ${\boldsymbol C}_{( {\boldsymbol P} ) }^\kappa$ [Reference Meyer and Held17]. In an easy interpretation, the limit κ = 0 corresponds to no mixing between different age groups, i.e. the diagonal contact matrix C(P) = I (Fig. 3c). When κ = 1, the contact matrix represents the given projected contact matrix (Fig. 3d). As κ → ∞, the transmission from an infected person to any individual of any age group has the same distribution with other groups regardless of the group they are in [Reference Meyer and Held17]. We also consider homogenous mixing scenario in the epidemic component. Second, the non-negative weight ${\cal W}_{{r}^{\prime}r}$ in the epidemic component describes the strength of transmission between geographical units. In the absence of mobility data, it can be estimated using a power law formulation in terms of adjacency order $o_{{r}^{\prime}r}$, which is a discrete distance measure of neighbourhood order between unit r and r [Reference Meyer and Held25]. The power law weights ${\cal W}_{{r}^{\prime}r} = ( {o_{{r}^{\prime}r} + 1} ) ^{{-}d}$, where d > 0 is the decay parameter to be estimated, thus give unit weight to local transmission when r  =  r and then decay to promote the spatial transmission from unit r to unit r. The power law weights can be age-dependent (replacing d by $d_{{g}^{\prime}}$) [Reference Meyer and Held17]. In this study, $o_{{r}^{\prime}r}$ ranges from 0 to 7.

All procedures were performed using R software version 4.0.5, packages surveillance version 1.19.1 [Reference Meyer, Held and Höhle28] and hhh4contacts version 0.13.1 [Reference Meyer and Held17]. In each model, maximum likelihood estimates of parameters and 95% confidence intervals (95% CIs) were obtained numerically. Model selection is performed according to the smallest Akaike information criterion (AIC) value.

Sensitivity analysis

We performed a sensitivity analysis using weekly aggregation of the surveillance data. We also ran another sensitivity analysis to assess the impact of different forms of contact matrix on our results, including the original contact matrix, and the per capita contact rates (i.e. dividing the mean number of contacts per day per participant in group g to the Vietnamese population size in 2009 and in 2019 [20] in contact group g).

Ethical consideration

As part of public health surveillance system in Vietnam, case-based data of measles were routinely collected for disease control purposes. Anonymised data, i.e. without identification of patient information, were provided for use in this study. Therefore, this study did not require ethical approval.

Results

Table 1 summarises the age-stratified spatio-temporal models with respect to different assumptions of age-structured contact matrix and spatial transmission weights. Because the AIC values of two models with age-dependent power law (two last rows) are not largely different given the large sample size, we select the simplest model that incorporates the projected matrix C(P) (the second-to-last row) for further exploration. Coefficient estimates of the selected model are presented in Table 2. Overall, the disease transmission was dominated by transmission within age groups, which contributed to 59.9% of measles cases while the contribution of transmission between age groups was 35.5% of cases. The endemic component added the remaining 4.6% of total cases (Supplementary Fig. S1). The transmission within and between age strata are described in Table 3 and visualised in Figure 4. In the youngest age group, 74.9% of the disease cases were predominantly affected by within-age-group transmission whereas only 19.1% of the cases were explained by transmission from other age groups. In those aged 5–14 years, the contribution of within- and between-age-group transmission seemed balanced with 49.1% and 49.2% of disease incidence, respectively. Interestingly, as opposed to the spreading pattern of measles in the 0–4 years group, we found a large number of cases in the 15–24 years and 25+ years groups attributable to transmission from other age groups. Specifically, an estimated 48.1% of cases aged 15–24 years and 57.6% of cases aged 25+ years were infected by age group 0–4 years, respectively, whereas transmission within age groups contributed to 13.1% of cases aged 15–24 years and 19.2% of cases aged 25+ years.

Table 1. Summary of age-stratified spatio-temporal models for surveillance data of measles in Southern Vietnam

The first two columns list the fitted models corresponding to different assumptions on spatial transmission weights and the projected age-structured contact matrix C(P). The endemic-only model in the first row contains the endemic component only.

Table 2. Estimated parameters, their 95% CIs and standard errors in the selected model (model with age-specific power law and projected contact matrix)

Table 3. Proportion (%) of cumulative measles cases estimated from the selected model that are attributable to endemic, within age group and from other age group transmission

Fig. 4. Fitted components of the selected model (i.e. model using the projected contact matrix C(P) and assumption of age-specific power law), aggregated by age group over all provinces. The dots indicate the observed number of daily infections.

When scaling the epidemic component with the population size, we found that the attraction to province r scaled slower than proportional with population size of age group g. The corresponding power of the population scaling factor was estimated at τ = 0.49 (95% CI 0.28–0.69). Moreover, the spatial diffusion of the disease across provinces followed the age-dependent power laws (Fig. 5). The group-specific decay parameter $d_{{g}^{\prime}}$ increases from 1.83 (95% CI 1.73–1.94) in the youngest to 3.30 (95% CI 2.87–3.78) in the oldest age groups, meaning that a stronger decay of transmission was observed for more distant provinces in older age groups. In other words, the spatial interaction of nearby provinces is more important to capture the dynamics of measles spread across age strata.

Fig. 5. Estimated spatial transmission weights between provinces by age group.

The overdispersion parameters corresponding to the counts in age groups 0–4 years, 5–14 years, 15–24 years and 25+ years groups in the selected model were estimated at 0.17 (95% CI 0.15–0.20), 0.31 (95% CI 0.25–0.36), 0.23 (95% CI 0.08–0.37) and 0.15 (95% CI 0.09–0.22), respectively. This implies that the assumption of Y grt following the negative binomial distribution is more suitable in the model than the Poisson distribution (ψ g = 0).

Results of the sensitivity analyses are presented in Supplementary Table S1. We found that the results are robust when applying to different contact matrices (the original and contact rate matrices) in the model. When we changed the resolution of data into weekly intervals (but keeping the projected contact matrix), the lowest AIC value was observed in the model with power-adjusted projected contact matrix and age-specific power law. The estimated power adjustment κ of this model was low (0.16; 95% CI 0.11–0.22), meaning that the transmission within age group in the epidemic component summarises more information than suggested in the projected contact matrix (Supplementary Figs S3B and S4). Nevertheless, without power adjustment of the (projected) contact matrix, the weekly aggregation resulted in a contribution of transmission of within and between age groups, similar to that of the main findings (Supplementary Fig. S5).

Discussion

Using a regression-oriented, endemic–epidemic time series model, we performed a detailed analysis of the transmission dynamics of measles outbreak with respect to age strata, time and space in Southern Vietnam during 2018–2020. Overall, the transmission of measles in the outbreak was built by the intricate reciprocity between different age strata across geographical regions.

It is apparent that measles is a childhood disease. Sixty-one per cent of the infections in the 0–4 years group indicated immunity gaps among these cohorts. This could be because they were not fully covered by two doses of MCV, which are currently administered at 9 and 18 months of age in Vietnam. Studies on the most recent outbreak in Vietnam (i.e. the 2013–2014 outbreak) indicated a high proportion of young children not accomplished two doses of MCV [Reference Cuong29] or had an insufficient level of protection against measles infection [Reference Choisy30]. Moreover, measles antibody levels in children vaccinated the first single dose, especially those received at 9–11 months, demonstrated a failure to induce an adequate effective immune response [Reference Carazo31]. This highlights the importance of compliance of two vaccine doses in age-eligible children to prevent them contracting measles. In addition, we must not overlook a substantial proportion of cases in older children, adolescents and adults. Although a stabilisation of the seroprevalence level until 10 years of age and a fluctuating seroprevalence level in people aged 10–20 years were observed, there were large discrepancies in seroprevalence level at the spatial scale, for example in Ho Chi Minh City a particularly low seroprevalence level in 16–17 years old was observed [Reference Choisy30]. Studies in China confirmed a significant decrease of seropositivity over time after vaccination in those aged from 6 to 14 years [Reference Yan32] and a lower sero-protection level in the 15–19 compared to 5–9 years groups [Reference He33]. However, older children and adolescents in our study could be unvaccinated in the national supplementary immunisation campaigns implemented in Vietnam in 2014–2015 although these activities targeted those aged 1–14 years (cohorts 2000–2013). Likewise, we suspected that adult cases, especially those aged 25–35 (accounted for 9.4% of total cases, data not shown) likely remained vulnerable because of missed vaccination during the introduction of measles immunisation programme (1983–1989) [Reference Sniadack34] rather than the result of waning immunity. Further evaluation on the age-specific immunity profile for measles is necessary. The need for supplementary immunisation strategies targeted in adolescents and young adults should be also considered to reduce the residual susceptibility in these populations.

Our study once again confirmed that a model incorporating social contact data has projected the infectious disease dynamics better than those with assumption of random mixing [Reference Bansal, Grenfell and Meyers10, Reference Mossong12, Reference Funk13]. From the model fitted, we were able to quantify the amount of within-group transmission and effectively capture ‘who acquired infection from whom’. This model helped to explain the measles transmission mechanism across age groups. Because of the age-assortative pattern of contact rates [Reference Horby11], an infected individual is more likely to transmit the disease to a susceptible person in their same age group. The increased within-group interaction amongst children aged 0–4 years increases the risk of infection in this group and thus may act as a driving factor of the outbreak. In addition, the role of school-aged children in facilitating disease spread, particularly in school settings, is important because of the high number of contacts within this subpopulation. Measles transmission in the school environment has been confirmed in a number of studies [Reference Becker35, Reference van Boven36]. When looking at the between-age group transmission, we observed that a substantial number of measles cases in older age strata, especially in the adult group (57.6%), was sourced from the 0–4 years group. The projected contact matrix implies that mixing rates are high between this age group and the age group of their parents and that it is likely that these parents have been exposed to measles and acquire infection from their children. Clustering of disease susceptibility within households can boost the likelihood and the persistence of disease outbreaks [Reference Liu9, Reference Kuylen37]. Therefore, we recommend more in-depth analyses on measles transmission in high-contact settings (e.g. households and schools) in future work.

Our study provided insights into the spatial interaction between different geographical units in disease transmission. We found an agglomeration effect that measles incidence in the epidemic component scaled (slower) with the population size of the ‘importing’ age stratum g in province r. Since long-distance human movement has an important role in disease diffusion, applying the age-dependent power law formulation was appropriate in shaping the spatial interaction across age strata in relation to different neighbourhood orders [Reference Meyer and Held25, Reference Geilhufe38]. We observed that in the 0–4 years group, the power law puts more weights on local and first-order neighbour transmissions than in other age groups, which experienced the faster distance decay of transmission from the nearest neighbour. This implied that infections in older age groups were more likely to happen within their (provincial) home residence whereas cases in young children possibly depended on past cases from the same or neighbouring provinces. Although power law approximation is helpful to investigate disease spread [Reference Geilhufe38], network data (e.g. local road, air data) could be conceivably taken into account as they could be a good proxy for the stochastic human transportation. Unfortunately, we did not have such data available for our study. We suggest that future research addresses this gap to yield further understanding in the spatial disease spreading.

The high number of infected persons among young children suggests that continuation of the routine two-dose vaccination programme for this group is critical. Furthermore, catch-up campaigns at the local rather than national level should be considered, and the focus should be on older age groups. This serves not only to improve local vaccination coverage across a broader age spectrum but also to reduce the risk that susceptible individuals, who may group together in schools and households, for example, may become infected through transmission from other age groups. We also suggest that health communication should receive more attention in future control measures, such as caution for school children and parents for better prevention of measles transmission in those environments.

We recorded several limitations in our study. First, our model was restricted with an autoregression on cases at previous time t − 1 but neglected cases at larger lags, which may improve the model fit [Reference Bracher and Held39]. However, our sensitivity analysis using weekly counts, which may better reflect the serial interval of measles, resulted in similar conclusions. Second, we relied on the number of contacts between strata calculated from a survey in Northern Vietnam anno 2007; this may not reflect the ‘true’ contact patterns in the Southern region. When more social contact data become available, we could also take into account the characteristics of contact networks in space (e.g. location of contact) and time (e.g. duration of contacts) as they may provide more information in the spatial disease spread [Reference Wallinga, van de Kassteele, Hens, Held, Hens, O'Neill and Wallinga40]. Besides, higher reporting rates in children may explain the prevailing number of infections in younger age groups. Our model may, thus, underestimate the incidence in younger children and overestimate the incidence in older groups. The impact of such underreporting on the endemic–epidemic model is an important topic of future research. Finally, we did not consider local vaccination coverage and how immunity levels vary, for example because of previous outbreaks, as model inputs to infer the level of susceptibility. This is certainly a topic of interest when sufficient data are available.

In summary, we used an age-structured endemic–epidemic model of infectious disease counts to have insights into the transmission dynamics of measles in Southern Vietnam, based on measles surveillance data. In young children, within-age-group transmission was dominant whereas between-age-group transmission had stronger effects among older age groups. Furthermore, local and first-order neighbour transmission played a critical role in the diffusion of the disease despite age groups. Our study findings could be useful for age-targeted measles control in future as it gives insights into high-risk subgroups and key factors that are critical to the transmission dynamics (e.g. contacts between age groups, spatial interaction).

Supplementary material

The supplementary material for this article can be found at https://doi.org/10.1017/S0950268822001431

Acknowledgements

We are grateful to the VLIR-UOS for awarding THTN a scholarship to study the Master of Epidemiology at the University of Antwerp, Belgium. We acknowledge support from the board of directors and colleagues at the Pasteur Institute in Ho Chi Minh City in providing surveillance data for analysis.

Author contributions

THTN participated in data collection, statistical analysis and interpretation of results and writing the draft of the manuscript. CF and NH participated in the study conception, supervision and critical review of the manuscript. All authors approved the final version of the manuscript.

Financial support

This research received no specific grant from any funding agency, commercial or not-for-profit sectors.

Conflict of interest

The authors have no competing interests to declare.

Data availability statement

Raw data were generated at the Pasteur Institute in Ho Chi Minh City, Vietnam. Derived data supporting and codes for reproducibility of the findings of this study are available at https://github.com/trangnguyenpmd/measlesVietnam_agestratified_model.

References

Gay, NJ (2004) The theory of measles elimination: implications for the design of elimination strategies. The Journal of Infectious Diseases 189, S27S35.Google ScholarPubMed
Patel, MK et al. (2020) Progress toward regional measles elimination – worldwide, 2000–2019. Morbidity and Mortality Weekly Report (MMWR) 69, 17001705.CrossRefGoogle ScholarPubMed
Trentini, F et al. (2017) Measles immunity gaps and the progress towards elimination: a multi-country modelling analysis. The Lancet Infectious Diseases 17, 10891097.CrossRefGoogle ScholarPubMed
Glasser, JW et al. (2016) The effect of heterogeneity in uptake of the measles, mumps, and rubella vaccine on the potential for outbreaks of measles: a modelling study. The Lancet Infectious Diseases 16, 599605.CrossRefGoogle ScholarPubMed
Herzog, SA, Paul, M and Held, L (2011) Heterogeneity in vaccination coverage explains the size and occurrence of measles epidemics in German surveillance data. Epidemiology and Infection 139, 505515.CrossRefGoogle ScholarPubMed
Qin, S et al. (2019) Measles in Zhejiang, China, 2004–2017: population density and proportion of floating populations effects on measles epidemic. Health Security 17, 193199.CrossRefGoogle ScholarPubMed
Parpia, AS et al. (2020) Spatio-temporal dynamics of measles outbreaks in Cameroon. Annals of Epidemiology 42, 6472, e63.CrossRefGoogle ScholarPubMed
Wallinga, J, Teunis, P and Kretzschmar, M (2006) Using data on social contacts to estimate age-specific transmission parameters for respiratory-spread infectious agents. American Journal of Epidemiology 164, 936944.CrossRefGoogle ScholarPubMed
Liu, F et al. (2015) The role of vaccination coverage, individual behaviors, and the public health response in the control of measles epidemics: an agent-based simulation for California. BMC Public Health 15, 447.CrossRefGoogle ScholarPubMed
Bansal, S, Grenfell, BT and Meyers, LA (2007) When individual behaviour matters: homogeneous and network models in epidemiology. Journal of The Royal Society Interface 4, 879891.CrossRefGoogle ScholarPubMed
Horby, P et al. (2011) Social contact patterns in Vietnam and implications for the control of infectious diseases. PLoS One 6, e16965e16965.CrossRefGoogle ScholarPubMed
Mossong, J et al. (2008) Social contacts and mixing patterns relevant to the spread of infectious diseases. PLoS Medicine 5, e74.CrossRefGoogle Scholar
Funk, S et al. (2019) Combining serological and contact data to derive target immunity levels for achieving and maintaining measles elimination. BMC Medicine 17, 180.CrossRefGoogle ScholarPubMed
Hens, N et al. (2015) Assessing the risk of measles resurgence in a highly vaccinated population: Belgium anno 2013. EuroSurveillance 20, 20998.CrossRefGoogle Scholar
Held, L, Höhle, M and Hofmann, M (2005) A statistical framework for the analysis of multivariate infectious disease surveillance counts. Statistical Modelling 5, 187199.CrossRefGoogle Scholar
Meyer, S and Held, L (2017) Incorporating social contact data in spatio-temporal models for infectious disease spread. Biostatistics (Oxford, England) 18, 338351.Google ScholarPubMed
Vietnam Ministry of Health. Circular: Guidance on notification, reporting and declaration of communicable diseases, number: 54/2015/TT-BYT, Hanoi (Vietnam).Google Scholar
World Health Organization (2017) Joint external evaluation of IHR core capacities of Viet Nam: mission report: 28 October–4 November 2016, p. 25.Google Scholar
General Statistics Office of Vietnam. The completed results of the Vietnam population and housing census. Available at http://tongdieutradanso.vn/12-completed-results-of-the-2019-census.html, https://www.gso.gov.vn/du-lieu-va-so-lieu-thong-ke/2019/03/ket-qua-toan-bo-tong-dieu-tra-dan-so-va-nha-o-viet-nam-nam-2009/ (Accessed 29 Jan 2021).Google Scholar
Willem, L et al. (2020) SOCRATES: an online tool leveraging a social contact data sharing initiative to assess mitigation strategies for COVID-19. BMC Research Notes 13, 293.CrossRefGoogle ScholarPubMed
Arregui, S et al. (2018) Projecting social contact matrices to different demographic structures. PLoS Computational Biology 2018, e1006638.Google Scholar
Paul, M and Held, L (2011) Predictive assessment of a non-linear random effects model for multivariate time series of infectious disease counts. Statistics in Medicine 30, 11181136.CrossRefGoogle ScholarPubMed
Held, L and Paul, M (2012) Modeling seasonality in space-time infectious disease surveillance data. Biometrical Journal 54, 824843.CrossRefGoogle ScholarPubMed
Meyer, S and Held, L (2014) Power-law models for infectious disease spread. Annals of Applied Statistics 8, 16121639.CrossRefGoogle Scholar
Held, L, Meyer, S and Bracher, J (2017) Probabilistic forecasting in infectious disease epidemiology: the 13th Armitage lecture. Statistics in Medicine 36, 34433460.CrossRefGoogle ScholarPubMed
Xia, Y, Bjørnstad, ON and Grenfell, BT (2004) Measles metapopulation dynamics: a gravity model for epidemiological coupling and dynamics. The American Naturalist 164, 267281.CrossRefGoogle ScholarPubMed
Meyer, S, Held, L and Höhle, M (2017) Spatio-temporal analysis of epidemic phenomena using the R package surveillance. Journal of Statistical Software 77, 155.CrossRefGoogle Scholar
Cuong, HQ et al. (2019) Gap in measles vaccination coverage among children aged 9 months to 10 years in Ho Chi Minh City, Viet Nam, 2014. Western Pacific Surveillance and Response Journal 10, 3945.CrossRefGoogle Scholar
Choisy, M et al. (2019) Sero-prevalence surveillance to predict vaccine-preventable disease outbreaks: a lesson from the 2014 measles epidemic in Northern Vietnam. Open Forum Infectious Diseases 6, ofz030.CrossRefGoogle ScholarPubMed
Carazo, S et al. (2020) Effect of age at vaccination on the measles vaccine effectiveness and immunogenicity: systematic review and meta-analysis. BMC Infectious Diseases 20, 251.CrossRefGoogle ScholarPubMed
Yan, R et al. (2019) Study on factors associated with seroprotection after measles vaccination in children of 6–14 years in Eastern China. Vaccine 37, 51855190.CrossRefGoogle Scholar
He, H et al. (2013) Waning immunity to measles in young adults and booster effects of revaccination in secondary school students. Vaccine 31, 533537.CrossRefGoogle ScholarPubMed
Sniadack, DH et al. (2011) Epidemiology of a measles epidemic in Vietnam 2008–2010. The Journal of Infectious Diseases 204, S476S482.CrossRefGoogle ScholarPubMed
Becker, AD et al. (2016) Estimating enhanced prevaccination measles transmission hotspots in the context of cross-scale dynamics. Proceedings of the National Academy of Sciences of the United States of America 113, 1459514600.CrossRefGoogle ScholarPubMed
van Boven, M et al. (2010) Estimation of measles vaccine efficacy and critical vaccination coverage in a highly vaccinated population. Journal of the Royal Society Interface 7, 15371544.CrossRefGoogle Scholar
Kuylen, E et al. (2020) Clustering of susceptible individuals within households can drive measles outbreaks: an individual-based model exploration. Scientific Reports 10, 19645.CrossRefGoogle ScholarPubMed
Geilhufe, M et al. (2014) Power law approximations of movement network data for modeling infectious disease spread. Biometrical Journal 56, 363382.CrossRefGoogle ScholarPubMed
Bracher, J and Held, L (2022) Endemic–epidemic models with discrete-time serial interval distributions for infectious disease prediction. International Journal of Forecasting 38, 12211233.CrossRefGoogle Scholar
Wallinga, J, van de Kassteele, J and Hens, N (2019) Chapter: Contact patterns for contagious diseases. In Held, L, Hens, N, O'Neill, P and Wallinga, J (eds), Handbook of Infectious Disease Data Analysis. New York: Chapman and Hall/CRC, Taylor & Francis Group, LLC, pp. 105107.Google Scholar
Figure 0

Fig. 1. Evolution of age-specific measles cases by date of symptom onset (left axes) and incidence per 100 000 population by month (blue lines, right axes) in Southern Vietnam, 1 January 2018 to 30 June 2020. Lunar New Year in 2019 and 2020 are highlighted in red.

Figure 1

Fig. 2. Maps of age-specific cumulative incidence per 100 000 population in Southern Vietnam, 1 January 2018 to 30 June 2020.

Figure 2

Fig. 3. (a) Original age-structured contact matrix C estimated in Northern Vietnam anno 2007 aggregated to the age groups of interest and (b) the age-structured contact matrix projected for Southern Vietnam C(P) based on (a). The entries contain the mean number of contacts made by one participant per day. (c), (d), (e) and (f) refer to the power transformation of row-normalised contact matrix C(P) for different values of κ.

Figure 3

Table 1. Summary of age-stratified spatio-temporal models for surveillance data of measles in Southern Vietnam

Figure 4

Table 2. Estimated parameters, their 95% CIs and standard errors in the selected model (model with age-specific power law and projected contact matrix)

Figure 5

Table 3. Proportion (%) of cumulative measles cases estimated from the selected model that are attributable to endemic, within age group and from other age group transmission

Figure 6

Fig. 4. Fitted components of the selected model (i.e. model using the projected contact matrix C(P) and assumption of age-specific power law), aggregated by age group over all provinces. The dots indicate the observed number of daily infections.

Figure 7

Fig. 5. Estimated spatial transmission weights between provinces by age group.

Supplementary material: File

Nguyen et al. supplementary material

Nguyen et al. supplementary material

Download Nguyen et al. supplementary material(File)
File 5.7 MB