 Research
 Open access
 Published:
Spatiotemporal analysis of mortality among children under the age of five in Manhiça (Mozambique) during the period 19972005
International Journal of Health Geographics volume 10, Article number: 14 (2011)
Abstract
Background
Reducing childhood mortality is the fourth goal of the Millennium Development Goals agreed at the United Nations Millennium Summit in September 2000. However, childhood mortality in developing countries remains high. Providing an accurate picture of space and timetrend variations in child mortality in a region might generate further ideas for health planning actions to achieve such a reduction. The purpose of this study was to examine the spatiotemporal variation for child mortality rates in Manhiça, a district within the Maputo province of southern rural Mozambique during the period 19972005 using a proper generalized linear mixed model.
Results
The results showed that childhood mortality in all the area was modified from year to year describing a convex timetrend but the spatial pattern described by the neighbourhoodspecific underlying mortality rates did not change during the entire period from 1997 to 2005, where neighbourhoods with highest risks are situated in the peripheral side of the district. The spatial distribution, though more blurred here, was similar to the spatial distribution of child malaria incidence in the same area. The peak in mortality rates observed in 2001 could have been caused by the precipitation system that started in early February 2000, following which heavy rains flooded parts of Mozambique's southern provinces. However, the mortality rates at the end of the period returned to initial values.
Conclusions
The results of this study suggest that the health intervention programmes established in Manhiça to alleviate the effects of flooding on child mortality should cover a period of around five years and that special attention might be focused on eradicating malaria transmission. These outcomes also suggest the utility of suitably modelling spacetime trend variations in a region when a point effect of an environmental factor affects all the study area.
Background
Reducing childhood mortality (mortality before the age of five) is the fourth goal of the Millennium Development Goals agreed at the United Nations Millennium Summit in September 2000. However, childhood mortality in developing countries remains high: it has been estimated that about 10.6 million children die each year, although most of these deaths could be prevented by public health interventions [1–3]. Therefore, the quality of a health system in a country or region is a crucial issue when it comes to ensuring the success of health campaigns developed to decrease such mortality. Unfortunately, most developing countries have poorlyfunctioning systems for monitoring life events; for example, in Africa only 30% of births are registered [4].
Manhiça, a district within the Maputo province of southern rural Mozambique, is covered by a continuous demographic surveillance system (DSS) that since 1996 has been run by the Health Research Centre of Manhiça (CISM). Details about the census and followup procedures are described by Alonso et al. [[5], p. 189195]. The DSS has proved to be an adequate tool for reporting accurate demographic measures for southern rural Mozambique [6]. Moreover, providing an accurate picture of spacetime variations in child mortality in the district might generate further ideas for health planning actions in Manhiça. In this regard, modelling the temporal variability in childhood mortality would help health researchers to understand the relationship between this mortality and events that may vary from year to year, for example, climatic conditions. In terms of spatial variability, areas with high mortality risks would require special health strategies that are different to those in areas with lower risks.
In spatial mortality mapping the data used are often aggregated and comprise death counts within a lattice, which might be health areas or administrative zones. It should be noted here that when the spatial lattice involves small areas the use of crude measures such as the standardised mortality rate is likely to yield unacceptably large standard errors or suggest extreme risks that misrepresent the real risk heterogeneity among areas and time [7]. These problems are usually overcome by applying smoothing methods such as the Poisson regression mixed model (PRMM) [8]. The PRMM includes a random effect for each area under study with a certain prior distribution that can accommodate the real risk heterogeneity among areas, or the spatial dependence of the data due to common unmeasured risk factors which contiguous areas might share. A widespread prior choice for the random effects in this kind of study is what is known as the conditional autoregressive model [9, 10] (PRMMCAR). If in addition of spatial variability one aims to evaluate the timetrend evolution of these areas one can extend the PRMMCAR model by including a plausible function depending on time in the linear predictor of the model. Bernardinelli et al.[7] extended the PRMMCAR model to consider a linear time trend in their analysis. The authors proposed to include random effects for both the areaspecific intercept and time trends. By including a linear time trend in space the estimates of an areaspecific trend can borrow strength from related areas, thus resulting in more sensitive estimates when data are scarce.
The present study evaluates the spatiotemporal variation in childhood mortality in the village of Manhiça and its outskirts during the period 19972005, using a modified version of the spacetime trend variation model proposed by Bernardinelli et al.[7] to model appropriately our mortality data.
Methods
Study area
The study was conducted in the village of Manhiça and its outer reaches which is located in Maputo province, southern Mozambique, during the period January 1997 to December 2005.
The village of Manhiça, 25°24'S and 32°48'E, is situated in an area of flat, bush savannah along the coast of Mozambique; it is 80 km north of the capital Maputo and covers approximately 120 km^{2}. Geographic characteristics, climatological conditions and population living customs in Manhiça have been described in detail by Abellana et al.[11].
The study area is subdivided for politicaladministrative reasons into 115 small neighbourhoods. Maps of the area were obtained from the Direção Nacional de Geografia e Cadastro of Mozambique (reference numbers: SG36/IINE page 1169 2532, SG36/JINO page 1170 2533A1, SE26/VIIISO page 1178 2532B3, SG36/IIVSO page 1179 2532B4). The maps were scanned and the limits of the neighbourhoods were georeferenced by the Manhiça Health Research Centre (CISM).
Study subjects
Data were collected via the demographic surveillance system (DSS) which has been operating and run by the CISM in Manhiça since 1996. During surveillance every household is visited at least twice a year and life events including births, deaths and migrations are recorded. Other events such as pregnancies, abortions, stillbirths and level of education are also documented during the visits, as are the characteristics of household construction. Since sixmonthly visits could lead to the omission of some events the information recorded was complemented through weekly updates by the key informants in the community, as well as via daily hospital visits.
The information collected from the DSS regarding children consisted in birth date, gender, neighbourhood of residence, and, in the case of death, the date of this event.
Each child included in the analysis had to have resided in the study area during the period 19972005, while the time at risk for each child in each year was defined as the number of days that the child was alive during that year and aged below five years old.
We also collected sociodemographic indicators at the neighbourhood level, for example, the percentage of illiterate mothers in the specific neighbourhood, percentage of households with a WC, percentage of households with a kitchen, percentage of cane households and percentage of households with a single construction. These covariates were categorised as quartiles to facilitate the identification of any association patterns with the mortality rates.
Standardised mortality rates
Annual standardised mortality ratios (SMR) at both district (i.e., Manhiça and its outskirts) and neighbourhood level were determined. To obtain the annual expected number of deaths, genderspecific mortality rates (calculated as the number of deaths divided by the number of childrenperday at risk in each gender group in the specific year under consideration when district level is the goal, or year and neighbourhood when neighbourhood level is the objective) were multiplied by the sum of childrenperday at risk in each gender group across the whole period from 1997 to 2005 and across all neighbourhoods. Therefore, SMRs that deviate from 1 show which years, or neighbourhoods in a specific year, have higher/lower mortality rates than the constant average across all the study area and over the period analysed.
Exploratory analysis
Global timetrend
For modelling purposes one usually assumes that death counts are Poisson distributed. Therefore, generalised linear models (GLM) are applied, where the canonical function that links death counts to the linear predictor is the logarithm, and the logexpected counts are included into the model as an offset. This model is commonly termed the Poisson regression model (PRM). Hence, we conducted a timetrend exploratory analysis by plotting the logtransformed SMRs (logSMR) for each year for the district of Manhiça revealing a marked increase followed by decreased shape of the crude logSMR, thus indicating that the most plausible model includes time in the analysis by using a secondorder polynomial time trend, i.e. log SMR = f(t,α) = α_{0} + α_{1}t + α_{2}t^{2}.
Therefore, if Y_{ it }and E_{ it }are the number of deaths and expected counts respectively, in the ith neighbourhood and tth year, and we denote by μ_{ it }the expected value of Y_{ it }, i.e., μ_{ it }= E(Y_{ it }), then the PRM (which will be referred as Model 0) is defined as:
where α_{0} represents the baseline logrelative mortality risk across all neighbourhoods and α_{1} and α_{2} stand for the global logrelative mortality rate evolution. In order to avoid possible colinearity between α_{1} and α_{2} in model parameter estimates, t was constructed to range discretely from 4 to 4, and thus t and t^{2} are orthogonal vectors. This is simply a year translation in which the midpoint of the period, 2001, is taken as the translation value. Thus, 2001 becomes the artificial value of 0 and therefore the baseline year in the analysis, while 4 corresponds to 1997 and 4 to 2005. Note that if α_{1} and α_{2} are estimated to be 0 it would mean that no changes in mortality rates would be observed across the period. If only α_{2} is estimated to be 0 a linear timetrend would be observed, and the sign of α_{1} would indicate whether there had been a linear increase or decrease in mortality rates. Otherwise, if α_{2} is estimated to be significantly different from 0 then a curved evolution is detected, and its sign stands for the convexity or concavity of the time evolution in mortality rates.
Finally, β is the vector of covariate parameters (in our analysis correspond to the sociodemographic indicators) and x_{i} corresponds to the ith row of the design matrix. The exponential of β (e^{β}) is referred as the covariatespecific relative risk. Likelihoodratio tests were used to decide which sociodemographic indicators would be included in the final model.
Spatiotemporal variability
In order to explore whether there was a common timetrend function or whether there were some neighbourhoods in which specific timetrends deviated from this global tendency, a PRM including the timetrend function for each neighbourhood was conducted. Here, therefore, the dependent variable was the number of deaths per year in the specific neighbourhood under consideration.
From the 115 PRM models adjusted separately for each neighbourhood we obtained 115 estimates about intercept (α_{0}), first (α_{1}) and secondorder (α_{2}) polynomial coefficient estimates, thus describing the specific timetrend for each neighbourhood. When a high variability was observed this indicated the need to include random effects in the PRM.
To explore the possible spatial dependency among neighbourhoods for both neighbourhoodspecific intercepts and neighbourhoodspecific time trend we calculated the Moran I test [12] for spatial autocorrelation among the 115 estimates of each element of the α vector (α_{0}, α_{1} and α_{2} respectively). If this spatial dependence assumption was not reasonable, random effects were given an exchangeable prior function, i.e. random noise; otherwise, when a significant result was observed this recommended the inclusion of spatiallydependent random effects.
Data modelling: Poisson regression models with random effects
Following the exploratory results we applied Poisson regression mixed models (PRMM) accounting for neighbourhoodspecific random effects.
If we assume that the conditional mean mortality count for the ith neighbourhood and tth year given the random effect vectors b = (b_{1},...,b_{ J }), with J being the number of random effects vectors to be considered in the analysis, is given by μ_{ it }= E(Y_{ it } b), then the PRMM is specified as:
In the event of spatial dependence we applied the improper conditional autoregressive joint distribution (ICAR) [13, 14] which induces 'local' smoothing by complete borrowing strength from related neighbours:
where Q is the 115 × 115 matrix defining the neighbourhood structure. Here we adopted the common neighbourhood approach, which defines areas i and k as neighbours if they share a common boundary, meaning that a specific neighbourhood will borrow strength from contiguous neighbourhoods. Therefore, the diagonal elements of Q are equal to the number of neighbours of the specific neighbourhood, while offdiagonal elements will be 1 if the corresponding areas are neighbours and 0 otherwise. {\sigma}_{{S}_{j}}^{2} is the variance component reflecting the spatiallystructured variability.
In the event that spatial dependency was not reasonable exchangeable priors were applied:
where I is the 115 × 115 identity matrix and {\sigma}_{{H}_{j}}^{2} a nonstructured variance component.
Three different PRMMs accounting for a second order polynomial timetrend and neighbourhoodspecific random effects were applied. The first PRMM (Model 1) included random effects for neighbourhoodspecific intercepts with nonstructured variability. The second PRMM (Model 2) accounted for neighbourhoodspecific intercept random effects with ICAR prior function. Model 1 and 2 are defined as follows, and the difference relies in the joint distributional assumption of the random effects, exchangeable and ICAR for Model 1 and 2 respectively:
Here, b_{0i} represents the underlying logrelative mortality risk for the ith neighbourhood in the baseline year 2001, however, since no other random effects are included into the model and b_{0i} are independent from both timetrend and covariates, b_{0i} are interpreted as the underlying logrelative mortality risks constant for the whole period considered.
A third model (Model 3) was also conducted which accounted as well for curvature timetrend random effects with exchangeable prior functions:
were b_{1i} and b_{2i} are the neighbourhoodspecific deviation trends from the overall trend explained by the fixed effects α_{1} and α_{2}. Note that predictions about α_{2} + b_{2}_{ i }illustrate the sharpness of the neighbourhoodspecific curvatures.
The exponential of the sum of all elements in the linear predictor of a PRMM is referred as the neighbourhoodspecific relative risk in the explicit year.
The PRMM parameters were estimated using the penalised quasilikelihood (PQL) approach [15].
For inference about neighbourhoodspecific underlying relative risks, prediction intervals about the random effects predictions were applied according to the approach proposed by Escaramís et al.[16]. When predictions of the random effects are significantly different from 0, the prediction of the underlying neighbourhoodspecific relative risk will have a 100(10.05)% prediction interval entirely above or below 1, where 0.05 is the type I error.
The quasilikelihood version of the Schwarz (BIC) information criterion [17] was used as a rule of thumb to discriminate between models [[18] (sect. 6.4), 19 (sect. 15.2)]. We also estimated the dispersion parameter of the resulting PRMM. This parameter estimate is a goodnessoffit measure in Poisson regression models, since it tells us how close the theoretical variability of the variable analysed is to the estimated variability through the model. Therefore, if both variabilities are equal then the dispersion parameter should be estimated to be 1, and therefore the distributional assumption of the model holds.
Model 3 is a modified version of the spacetime trend variation model proposed by Bernardinelli et al.[7] in the sense that incorporates a convex timetrend via a secondorder polynomial specification in the linear predictor instead of a linear timetrend, thus letting the model appropriately fit the steep increase followed by the steep decrease of the global timetrend evolution of our mortality data. Furthermore Bernardinelli et al.[7] argue the use of full Bayesian approaches, such as Markov Chain Monte Carlo (MCMC), for model parameter estimates in order to take into account the uncertainty in inference about underlying relativerisks predictions that arises from having to estimate variance components instead of pluggingin true values into the predictors. We have here taken benefit of the PQL technique in terms of lower CPU time consumption against MCMC methods by using Escaramís et al. [16] approach for inference about underlying relativerisk predictions. This approach is based on an analytical adjustment of such uncertainty and has been shown to provide accurate interval predictions when using the PQL technique to obtain model parameter estimates.
The models were fitted using the SAS software with the GLIMMIX procedure [20] and details on the syntax used are given in Additional file 1.
Results
Data description
The mean population count for the study area over the period considered was 9013 children below the age of five (range: 7287 in 1997 to 10,025 in 2004). Population per neighbourhood ranged from a mean of 18 children per year to a mean of 499.
The mortality rate reached a peak of 42 cases per 1000 children/year in 2001, with the lowest values being found at either end of the period (27 and 26 cases per 1000 children/year in 1997 and 2005, respectively).
Of all the sociodemographic indicators considered in our study only households with a single construction showed a significant association: those neighbourhoods with a lower percentage of single constructions showed an increased effect on child mortality rates (Table 1).
Exploratory results for our data showed a mean timetrend convex curvature among southern Manhiça neighbourhoods associated with the crude log SMR and revealing a marked increase followed by decreased shape (Figure 1, first plot in the grid). The estimated secondorder polynomial timetrend confirmed this result as the sign of the quadratic term is negative (Table 1 and Figure 1).
Time evolutions of the crude log SMRs for each of the 115 neighbourhoods are also shown in Figure 1. The plots include as well the smoothed timetrends derived from fitting the PRM for each neighbourhood. A high variability between trends is perceptible, however a high proportion of them seem to have undergone a convex time evolution in mortality rates. Boxplots in the last cell of the grid of Figure 1 are a resume of these neighbourhoodspecific smoothed timetrends; in particular the plots show the variability between neighbourhoods through their intercept, first and secondorder polynomial estimates. A high level of heterogeneity across neighbourhoods can be observed for the intercept estimates; however a lower variability is shown for the first and secondorder estimates. These results indicate the need to include random effects in the neighbourhoodspecific intercept in the final model but time trend appears to be constant across all neighbourhoods.
Furthermore, the 115 intercept estimates showed a significant autocorrelation (Moran's I = 4.1, p < 0.0001), whereas the 115 first and secondorder polynomial estimates did not (Moran's I = 1.181 and 0.224, respectively, with p = 0.119 and 0.411, respectively). These results suggested the presence of a common spatial pattern in the whole period analysed as the geographic variability of the intercept represents the baseline logmortality rate variability which is time independent. However the nonsignificant autocorrelation for the first and secondorder estimates indicated that the timetrend pattern of a specific neighbourhood may not depend on timetrend patterns from related neighbourhoods.
Data modelling
Results from the three PRMM models as well as the model without random effects (Model 0) are shown in Table 2. Model 0 exhibits overdispersion (ϕ = 1.218) which is clearly addressed by extending the PRM by including random effects in the linear predictor (Models 1, 2 and 3). According to the quasi BIC, Model 2 seems to capture the variability structure of the data better than Model 1 (BIC for Model 1 = 2713.22 vs BIC for Model 2 = 2704.94) revealing therefore that a spatial structure among neighbourhoods is present in childhood mortality rates in southern Manhiça. Model 3 extends Model 2 to take into account the timetrend variability in mortality rates among neighbourhoods. According to the results from this last model, the variability of the timetrend curvature among neighbourhoods is negligible since the variance for the first and secondorder polynomial random effects is almost 0. In addition the quasi BIC of Model 3 (BIC = 2711.24) is greater than the quasi BIC of Model 2, suggesting the use of Model 2 to analyse the data under the parsimonious rule.
Therefore Model 2 is selected to describe the data. This model shows to appropriately fit the theoretical Poisson variability of mortality counts as the dispersion parameter is very close to 1 (ϕ = 1.057). According to the model those neighbourhoods with the lowest percentage of households with a single construction had a significant risk effect on child mortality rates. The overall trend in child mortality rates for the period studied took a convex form, as the secondorder polynomial timetrend estimate is negative (α_{2} = 0.028(0.004)). The model also shows that the same spatiallystructured variability among neighbourhoods is present in the whole period analysed ({\sigma}_{S}^{2} = 0.094(0.030)). Therefore neighbourhoods that started with lower mortality rates in 1997 reached lower mortality rates in the middle of the period (2001) and reverse.
Figure 2 shows the two independent components of the model, the convex timetrend common for all neighbourhoods (bottomleft panel) and the common spatial pattern along the whole period (maps in righthand side), where neighbourhoods with highest underlying relative risks are situated in the peripheral side of the district.
Figure 3 describes the spatiotemporal variability of the neighbourhoodspecific relative risks. For the sake of simplicity maps for the years 1997, 1999, 2001, 2003 and 2005 are shown, while the remaining years in the study period are taken as intermediate steps. It can be seen that the highest rates of child mortality are reached in 2001, although the situation returns to initial values in 2005, with a very similar spatial pattern along the whole period analysed, where the biggest cluster with lower relative risks is situated in the westcentral side of the district. The slight difference of the spatial pattern of the relative risks across years is due to the little changes of the sociodemographic indicators during the period under consideration.
Discussion
The present study evaluated the spacetime trend variations in the southern area of Manhiça district for the period 19972005.
The data were analysed using a Poisson regression mixed model (PRMM) that included a secondorder polynomial time trend. This model showed a correct fit to the steep increase from 1997 to 2001 followed by a steep decrease thereafter of the global mortality rates among the 115 neighbourhoods that comprise the southern Manhiça district. This model is similar to the linear spacetime trend variation model proposed by Bernardinelli et al.[7], which was also applied by Kleinsmidth et al.[21] to evaluate trends in malaria incidence rates in a small area in South Africa. Our model includes random effects for neighbourhoodspecific intercepts accounting for spatial dependence; however we did not find neighbourhoodspecific variability on timetrends. The inclusion of the spatial random effects with respect to baseline enables the data for each area to borrow strength from related areas across the whole period. The model can also readily detect those neighbourhoods with extreme underlying mortality risks present in all the study period by constructing prediction intervals of the neighbourhoodspecific random effect predictions. The underlying relative risks reflect the mortality risks that are not explained by known risk factors and the fact that they present a spatial structure also reflect unknown common environmental factors that contiguous neighbourhoods share.
Our model shows that a spatial distribution of childhood mortality is patent in all the study period, as shown in Figures 2 and 3. The neighbourhoods with the lowest rates are mainly clustered in the centrewest side of the district, and the tendency is towards higher in the periphery areas. This is better seen in Figure 2 map on the lefthand side where significantly higher underlying relative risks are all situated in the peripheral side of the district. Despite being more blurred in our mortality data, this spatial pattern is similar to the marked spatial pattern described by Abellana et al.[11] for the spatial distribution of malaria infection in children under the age of 10 years living in the area. These authors also found that children under five years of age are at the highest risk group of malaria infection. This is in accordance with the fact that a high percent of deaths of subSaharan children under the age of five is attributable to malaria [22]. Concretely, malaria due to Plasmodium falciparum is the main killer among children between 28 days to 4 years living in southern Manhiça [23]. However childhood deaths in the study area are also attributable to other causes such as malnutrition, diarrhoea, pneumonia or HIV/AIDS [23] that might spoil the specific spatial structure of malaria infection in children living in southern Manhiça.
The model also shows that all southern Manhiça has undergone a convex evolution in child mortality rates during the period 19972005, with a maximum being reached in 2001. This convexity pattern could have been caused by the precipitation system that started in early February 2000, and which saw heavy rain flood parts of Mozambique's southern provinces. In as little as three weeks the main river systems in Mozambique, from the Incomati River in the south to the Zambézia River in the centrenorth, exceeded their normal yearly flood rates by several fold. As a result, the surrounding villages were flooded, causing the worst damage in fifty years. Manhiça is crossed by the Incomati River from north to south and was one of the areas severely affected by the precipitation system. As can be seen in Figure 4 the annual rainfall in 2000 was markedly higher than the other annual rainfalls for the period analysed, reaching values above 3000 mm, whereas in other years it did not even reach 2000 mm. Rainfall was recorded by the climatology station located near CISM. Given that many of the causes of global child mortality in developing countries, including malaria, diarrhoea, acute respiratory infections and malnutrition, are highly sensitive to climatic conditions such as flooding, this may explain the higher mortality rates in the middle of our study period.
Conclusions
The study showed that the same geographical pattern of underlying childhood mortality rates was patent in Manhiça and its outskirts in all the study period from 1997 to 2005 and similar to the spatial distribution of childhood malaria infection, suggesting that special attention might be focused on eradicating malaria transmission in Manhiça to achieve the reduction of childhood mortality agreed in the Millennium Development Goals at the United Nations Millennium Summit in September 2000 [24].
The study also showed that childhood mortality in Manhiça was modified from year to year describing a convex timetrend during the period, a common pattern for all the neighbourhoods that comprise the area, where the peak coincides with the precipitation system that started in early February 2000. However after approximately five years child mortality rates returned to initial values suggesting that health intervention programmes established in Manhiça to alleviate the effects of flooding on child mortality should cover a period of around five years. These outcomes suggest as well the utility of modelling spacetime trend variations in a region when a point effect of an environmental factor affects all the study area.
Abbreviations
 CAR:

conditional autoregressive model
 CISM:

Manhiça Health Research Centre
 PRMM:

Poisson regression mixed model
 SMR:

standardize mortality ratio
References
Victora CG, Wagstaff A, Schellenberg JA, Gwatkin D, Claeson M, Habicht JP: Applying an equity lens to child health and mortality: more of the same is not enough. Lancet. 2003, 362: 233241. 10.1016/S01406736(03)139177.
Bryce J, BoschiPinto C, Shibuya K, Black RE: WHO estimates of the causes of death in children. Lancet. 2005, 365: 11471152. 10.1016/S01406736(05)718778.
Jones G, Steketee RW, Black RE, Bhutta ZA, Morris SS: How many child deaths can we prevent this year?. Lancet. 2003, 362: 6571. 10.1016/S01406736(03)138111.
Stansfeld SK, Walsh J, Prate N, Evans T: Information to improve decision making for health. In Disease control priorities in developing countries. 2006, New York, Oxford University Press, 101730.
Alonso P, Saute F, Aponte JJ: Population and health in developing countries; vol.1, population, health and survival at INDEPTH sites. 2002, Ottawa: International Development Research Centre (IDCR)
Nhacolo AQ, Nhalungo DA, Sacoor CN, Aponte JJ, Thompson R, Alonso P: Levels and trends of demographic indices in southern rural Mozambique: evidence from demographic surveillance in Manhiça district. BMC Public Health. 2006, 6: 29110.1186/147124586291.
Bernadinelli L, Clayton D, Pascutto C, Montomoli C, Ghislandi M, Songini M: Bayesian analysis of spacetime variation in disease risk. Statistics in Medicine. 1995, 14: 243343. 10.1002/sim.4780142112.
McCulloch CE, Searle SR: Generalized, Linear, and Mixed Models. 2001, Canada: Wiley Series in Probability and Statistics
Besag J, York J, Mollié A: Bayesian image restoration, with applications in spatial statistics. Ann I Stat Math. 1991, 43: 159. 10.1007/BF00116466.
Pascutto C, Wakfield JC, Best NG, Richardson S, Bernardinelli L, Staines A, Elliott P: Statistical issues in the analysis of disease mapping data. Statistics in Medicine. 2000, 19: 24932519. 10.1002/10970258(20000915/30)19:17/18<2493::AIDSIM584>3.0.CO;2D.
Abellana R, Ascaso C, Aponte J, Saute F, Nhalungo D, Nhacolo A, Alonso P: Spatioseasonal modelling of the incidence rate of Malaria in Mozambique. Malaria Journal. 2008, 7: 22810.1186/147528757228.
Moran PAP: A test for spatial independence of residuals. Biometrika. 1950, 37: 178181.
Besag J: Spatial interaction and the statistical analysis of lattice systems. J R Stat Soc B. 1974, 36: 192236.
Sun D, Tsutakawa RK, Speckman PL: Posterior distribution of Hierarchical Models using CAR(1) Distributions. Biometrica. 1999, 86: 341350. 10.1093/biomet/86.2.341.
Breslow NE, Clayton DG: Approximate inference in generalized linear mixed models. Journal of the American Statistical Association. 1993, 88: 925. 10.2307/2290687.
Escaramis G, Carrasco JL, Ascaso C: Detection of Significant Disease Risks Using a Spatial Conditional Autoregressive Model. Biometrics. 2008, 64: 10431053. 10.1111/j.15410420.2007.00981.x.
Schwarz MD: Estimating the Dimension of a Model. Annals of Statistics. 1978, 6: 461464. 10.1214/aos/1176344136.
Verbeke G, Molenberghs G: Linear Mixed Models for Longitudinal Data. 2000, New York: SpringerVerlag
Molenberghs G, Verbeke G: Models for Discrete Longitudinal Data. 2005, New York: Springer
Littell RC, Milliken GA, Stroup WW: SAS® for Mixed Models. 2006, Cary, NC: SAS Institute Inc, 2
Kleinschmidt I, Sahrp B, Mueller I, Vounatsou P: Rise in Malaria Incidence Rates in South Africa: A smallArea Spatial Analysis of Variation in Time Trends. American Journal of Epidemiology. 2002, 155 (3): 257264. 10.1093/aje/155.3.257.
Rowe AK, Rowe SY, Snow RW, Korenromp EL, Schellenberg JRMA, Stein C, Nahlen B, Bryce J, Black RE, Steketee RW: The burden of Malaria mortality among African children in the year 2000. International Journal of Epidemiology. 2006, 35 (3): 691704. 10.1093/ije/dyl027.
Sacarlal J, Nhacolo AQ, Sigauque B, Nhalungo DA, Abacassamo F, Sacoor CN, Aide P, Machevo S, Nhampossa T, Macete EV, Bassat Q, David C, Bardaji A, Letang E, Saute F, Aponte JJ, Thompson R, Alonso PL: A 10 year study of the cause of death in children under 15 years in Manhiça, Mozambique. BMC Public Health. 2009, 9: 6710.1186/14712458967.
The Millennium Development Goals Report: United Nations. 2008,http://mdgs.un.org/unsd/mdg/Resources/Static/Products/Progress2008/MDG_Report_2008_En.pdfhttp://mdgs.un.org/unsd/mdg/Resources/Static/Products/Progress2008/MDG_Report_2008_En.pdf
Author information
Authors and Affiliations
Corresponding author
Additional information
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
GE, JLC and CA were responsible for statistical analysis and the preparation of the manuscript. JJA and PA conceived and designed the study. DN and AN were responsible for fieldwork and the geographical information system of Manhiça. JJA was responsible for data cleaning and manuscript preparation.
All authors read and approved the final manuscript.
Electronic supplementary material
12942_2010_408_MOESM1_ESM.DOC
Additional file 1:SAS syntax details. SAS syntax details for the Poisson regression mixed models parameter estimates. (DOC 25 KB)
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Rights and permissions
Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
About this article
Cite this article
Escaramís, G., Carrasco, J.L., Aponte, J.J. et al. Spatiotemporal analysis of mortality among children under the age of five in Manhiça (Mozambique) during the period 19972005. Int J Health Geogr 10, 14 (2011). https://doi.org/10.1186/1476072X1014
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/1476072X1014