Models for short term malaria prediction in Sri Lanka
 Olivier JT Briët^{1, 2}Email author,
 Penelope Vounatsou^{2},
 Dissanayake M Gunawardena^{3},
 Gawrie NL Galappaththy^{4} and
 Priyanie H Amerasinghe^{5}
https://doi.org/10.1186/14752875776
© Briët et al; licensee BioMed Central Ltd. 2008
Received: 23 October 2007
Accepted: 06 May 2008
Published: 06 May 2008
Abstract
Background
Malaria in Sri Lanka is unstable and fluctuates in intensity both spatially and temporally. Although the case counts are dwindling at present, given the past history of resurgence of outbreaks despite effective control measures, the control programmes have to stay prepared. The availability of long time series of monitored/diagnosed malaria cases allows for the study of forecasting models, with an aim to developing a forecasting system which could assist in the efficient allocation of resources for malaria control.
Methods
Exponentially weighted moving average models, autoregressive integrated moving average (ARIMA) models with seasonal components, and seasonal multiplicative autoregressive integrated moving average (SARIMA) models were compared on monthly time series of district malaria cases for their ability to predict the number of malaria cases one to four months ahead. The addition of covariates such as the number of malaria cases in neighbouring districts or rainfall were assessed for their ability to improve prediction of selected (seasonal) ARIMA models.
Results
The best model for forecasting and the forecasting error varied strongly among the districts. The addition of rainfall as a covariate improved prediction of selected (seasonal) ARIMA models modestly in some districts but worsened prediction in other districts. Improvement by adding rainfall was more frequent at larger forecasting horizons.
Conclusion
Heterogeneity of patterns of malaria in Sri Lanka requires regionally specific prediction models. Prediction error was large at a minimum of 22% (for one of the districts) for one month ahead predictions. The modest improvement made in short term prediction by adding rainfall as a covariate to these prediction models may not be sufficient to merit investing in a forecasting system for which rainfall data are routinely processed.
Background
Malaria has been a major public health problem in Sri Lanka [1] until recently. Since the year 2000, incidence has dwindled [2] with only 591 reported cases for 2006 [3]. It is unstable and fluctuates in intensity both spatially and temporally, thus resources for control have to be spread in time and space to be prepared for outbreaks, which have occurred in the past despite very aggressive and effective malaria control operations [4]. Having a forecasting system in place will contribute to a more focussed approach for control, and have a positive impact on the resource allocation for malaria control over space and time. This paper explores different models for malaria case prediction, which is possible due to the availability of long, dense and reliable records of malaria cases and climate variables in Sri Lanka [5].
While many factors play a role in the spatial and temporal distribution of malaria, climate variability (both spatial variation of the long term seasonal mean of weather variables, and temporal aberrations from the long term seasonal mean) has been shown to be important in explaining its occurrence [6–8] and is considered a major determinant [9]. Temperature, rainfall, and humidity affect breeding and survival of a certain (sub) species of anopheline mosquitoes that carry the malaria parasite, as well as development of malaria parasites within vector mosquitoes, thereby creating a link between weather and malaria.
At present, there are no practical tools for temporal prediction of the occurrence of malaria based on observed rainfall or weather forecasts in Asia, although these are in development [10]. For Africa, such tools have been developed [11] and applied [12]. Recent work [13, 14] focuses on malaria early warning systems, in which flags are raised when epidemics are expected. Setting the threshold for what is an epidemic (defined as a number of cases substantially exceeding that what is expected based on recent experience or what is thought normal) is subjective. The term epidemic does not combine well with the term prediction (if the expected number is predicted based on recent experience, the prediction can never be 'epidemic' according to the above definition). It is difficult to define, especially in Sri Lanka, at what level malaria incidence is thought to be normal, as the malaria time series show strong longterm fluctuations and it is, therefore, difficult to set thresholds. In general, disease forecasting is most useful to health services when it predicts case numbers two to six months ahead, allowing tactical responses to be made when disease risk is predicted to increase (or decrease) [15]. For this reason this paper avoids the problem of setting epidemic thresholds, and focuses on forecasting malaria cases.
Malaria case numbers are influenced by factors intrinsic to malaria such as infectivity, immunity and susceptibility of vectors and humans, and extrinsic, environmental factors such as rainfall. The number of possible models for malaria prediction is infinite. In biological process models, typically consisting of sets of equations, prediction can be done with details of all pathways, parameters and variables believed to be important for the dynamics of the disease [15]. In statistical models, temporal or spatial autoregressive terms account for the fact that case numbers depend on past or nearby case numbers through (sometimes cyclical) intrinsic processes, as well as for (unobserved) extrinsic auto correlated factors or factors with fading effects. This study was limited to some statistical models that are relatively easily implemented (without taking into consideration complex biological processes and their parameters), and/or that have been successful elsewhere in malaria forecasting studies. With sufficient temporal autocorrelation in malaria case time series, malaria cases can be predicted based on previous values [16]. However, predictions from statistical models are made under the assumption that the relationships established based on past observations remain the same in the future. Therefore, statistical models require experience with as wide a spectrum of conditions as possible. In this light, the present low case numbers, have been unprecedented in the time series under study, and a caution should be in place. More complex statistical models can be constructed where malaria incidence in an area is, apart from its own previous values, also dependent on (previous) values in neighbouring areas, or covariates such as rainfall [17, 18]. These latter models require more inputs and therefore more resource intensive to apply, particularly where covariate data need to be acquired and processed in a timely manner to be useful for forecasting. In this paper, it was examined which standard time series statistical model would be useful for forecasting malaria, and it was examined whether addition of rainfall to autoregressive models could improve malaria prediction in districts with one to four month forecasting horizons.
Methods
This section describes the data used for the analyses, methods for preprocessing of the data, types of models tested and the criteria for model selection.
Malaria data
The count of blood films examined for malaria as well as those positive for malaria per month reported by government health facilities and aggregated by medical officer of health (MOH) area (which represent sub district health administrative divisions) were provided by the Anti Malaria Campaign of Sri Lanka for the period 1972 – 2003. In addition, data aggregated by district were available for the years 2004 – 2005. For some of the records, the number of blood films examined was marked as "not received" (and therefore classified as missing). For 14.90% of the MOH area level records, the value was zero, or left blank. For the latter records, there was ambiguity as to whether the data value could be missing due to problems in data recording, or genuinely zero if no patients presented themselves for examination in that particular area in that particular month. As such, in a data cleaning procedure (see section on statistical methods), 1.4% of the records was declared as not available (NA) if the number of blood films examined was marked as "not received" (0.95%), or if the number of blood films could be classified as a lower additive outlier (0.44%). The data from districts in the north and east, where data gathering and reporting was affected by the armed conflict, had the largest percentage of data labelled not available: Jaffna (5.4%), Mannar (26.1%), Vavuniya (8.9%), Kilinochchi (2%), Trincomalee (2%) and Ampara (5.4%). After imputation, MOH area level data for positive cases were aggregated to district resolution and combined with the district level data (for the period 2004 – 005).
Rainfall data
Statistical methods
The monthly count of malaria positive blood slides in each district y_{ t }were transformed to normality via the logarithmic transformation z_{ t }= log (y_{ t }+ 1). The models tested included exponentially smoothing and autoregressive integrated moving average (ARIMA) models [20]. As some of the district malaria count time series showed strong seasonality, seasonality was also modelled. In models using exponential smoothing, seasonality was included using the HoltWinters procedure [20]. In ARIMA models, seasonality was included via three different approaches which are all widely used in literature: seasonality through fixed (monthly) effects; seasonality through harmonics; and through random effects using seasonal mixed autoregressive integrated moving average (SARIMA) models. Whether or not covariates such as rainfall and concurrent malaria case counts in neighbouring areas improved the predictive ability of the models was also tested. In addition, the seasonal adjustment method used by Abeku and colleagues [16], was tested.
Exponentially weighted moving average models
where a_{ t }, r_{ t }and S_{ t }are calculated by the following recursive functions:
a_{ t }= α(z_{ t } S_{ts}) + (1  α)(a_{t1}+ r_{t1});
r_{ t }= β(a_{ t } a_{t1}) + (1  β)r_{t1};
S_{ t }= γ(z_{ t } a_{ t }) + (1  γ)S_{ts}.
Both seasonal and nonseasonal (with γ fixed to 0) models were tested using the function "HoltWinters" in the package "stats" of the statistical software package "R".
(S)ARIMA regression models
It was assumed that z_{ t }is Gaussian distributed, z_{ t }~ N (μ_{ t }, σ^{2}), with mean μ_{ t }and variance σ^{2}. Further, it was assumed that
μ_{ t }= f(z_{ t }, d, p, x_{ t }) + g(u_{ t }, q) (2)
where f(z_{ t }, d, p, x_{ t }) and g(u_{ t }, q) model the temporal correlation as
f(z_{ t }, d, p, x_{ t }) = Φ_{ p }(B)(1  B)^{ d }(x_{ t } z_{ t }) + z_{ t }and g(u_{ t }, q) = Θ_{ q }(B)u_{ t } u_{ t }
where
Φ_{ p }(B) = 1  φ_{1}B  ...  φ_{ p }B^{ p };
Θ_{ q }(B) = 1  θ_{1}B  ...  θ_{ q }B^{ q };
u_{ t }is Gaussian white noise;
x_{ t }= m_{ t }+ S_{ t };
S_{ t }models the seasonal process;
m_{ t }models the mean of z_{ t }
B is a backshift operator with B^{ d }(z_{ t }) = z_{td}.
The seasonality in the ARIMA models of equation 2 was modelled by fixed effects. In particular it was assumed:

S_{ t }= 0 (A non seasonal model),

$\begin{array}{ccc}{S}_{t}={\displaystyle \sum _{}^{12}\left({\alpha}_{k}{\delta}_{k,t}\right)}& \text{where}& {\delta}_{k,t}=\{\begin{array}{ll}1\hfill & \text{ift}=\text{nk}\hfill \\ 0\hfill & \text{ift}\ne \text{nk}\hfill \end{array}\end{array}$
(Seasonality through fixed effects for months: Note that in this model m_{ t }does not contain an intercept to avoid over parameterisation),

${S}_{t}={\displaystyle \sum _{i}^{2}{A}_{i}\mathrm{sin}\phantom{\rule{0.5em}{0ex}}(2\pi {f}_{i}t+2\pi {\varphi}_{i})}$
a second order harmonic component where A_{ i }is the amplitude of harmonic i; f_{ i }is the frequency of harmonic i, with f_{1} = 1/s, f_{2} = 2/s; and ϕ_{ i }is the phase shift (in units of time) of harmonic i.
Also, a multiplicative seasonal ARIMA(p,d,q)*(P,D,Q) model (henceforth SARIMA) was considered with period s, obtained by modifying equation 2 into
μ = f(z_{ t }, d, p, D, P, s, m_{ t }) + g(u_{ t }, q, Q, s)
and Φ_{ p }(B), Θ_{ q }(B), u_{ t }, m_{ t }and B as explained above.
The function "arima" in the package "stats" of the statistical software "R" was used to calculate the prediction criterion. Tested models included all (Gaussian) ARIMA models possible with combinations of parameters (p, d, q) with p, q ∈ {0,1,2} and with d = 1, without explanatory variables, and all (Gaussian) SARIMA models possible with combinations of parameters (p, d, q, P, D, Q) with p, q ∈ {0,1,2} and d = 1 and P, D, Q ∈ {0,1}, also without explanatory variables. An intercept was not included in the mean as it drops out of the equation due to differencing (d = 1). The differencing also removes effects of trends such as potentially caused by population growth.
Covariates were included in the term m_{ t }. In particular, 1) ${m}_{t}={\displaystyle \sum _{j}{\beta}_{j}{z}_{j,t1}}$ where z_{j,t1}is the transformed malaria count at month t  1 in neighbour j; 2) m_{ t }= βχ_{tl}where χ_{ t }is the rainfall parameter in month tl with l = lag. Rainfall was considered at lags of one to four months preceding malaria and in the following forms: untransformed monthly rainfall, logarithmically transformed monthly rainfall, rainy day index (for those districts appropriate), monthly rainfall factored into quintiles (in case of nonlinear relationships), and rainfall with a separate coefficient for each of the twelve months, i.e. a coefficient for January rainfall, one for February, etc., in order to allow for seasonally varying effects. For each district, covariates were tested by including them into the (S)ARIMA model that performed best for the respective district and lag.
Estimation of nonavailable malaria count data
In a data cleaning procedure, the time series of blood film counts in MOH areas were logarithmically transformed to normality (after the value one was added to the data). Under the null hypothesis, each observation was assumed to be part of a seasonal autoregressive integrated moving average (SARIMA) process with parameters p = 0, d = 1, q = 1, P = 0, D = 1, and Q = 1. Observations were marked as additive outlier if the likelihood ratio test statistic (for an additive outlier) for the observation was below a threshold of 6 [21]. For those observations classified as not available or as a lower additive outlier that were not at the beginning or end of a series, values for the number of malaria positive blood films were estimated through a onestepahead SARIMA forecasting model on both the original series and on the reversed series, and the two estimates were averaged. This approach has been discussed by Mwaniki and colleagues [22]. Finally, the MOH area data series were aggregated to district resolution before analysis, as these spatial units remained constant over the study period, whereas for many MOH areas boundaries changed (within district boundaries) over the study period.
Seasonal adjustment method with last three observations
Model evaluation
For each district, model parameters were estimated on approximately the first half of the malaria case time series (January 1972 – December 1987), and one to four step ahead (out of sample) predictions were made on the second half (January 1988 – December 2005) with the parameters fixed.
where ${\stackrel{\u02c6}{y}}_{t}$ is the predicted number of malaria positive cases at time t, and N is the number of predictions. Predictions needed to be genuinely out of sample in order to prevent bias towards more parameter models. The (mare) was used rather than mean square error, as the malaria count time series show widely differing variances across the series [20]. The best model was that with the lowest prediction criterion for a given time series.
Results
Mean absolute relative error of out of series prediction at forecasting horizons of 1 to 4 months ahead for districts in Sri Lanka for the best (S)ARIMA model tested.
District  Horizon 1  Horizon 2  Horizon 3  Horizon 4  

Criterion  Model (pdqPDQ)  Criterion  Model (pdqPDQ)  Criterion  Model (pdqPDQ)  Criterion  Model (pdqPDQ)  
Ampara  0.37  012SOH  0.48  012101  0.58  012101  0.60  012101 
Anuradhapura  0.23  211101  0.37  210110  0.45  012110  0.51  210110 
Badulla  0.43  110SOH  0.62  111SOH  0.75  212101  0.74  112100 
Batticaloa  0.36  010011  0.54  012101  0.66  012101  0.78  012101 
Colombo  0.35  011000  0.38  112000  0.43  211001  0.46  011000 
Galle  0.49  212002  0.58  211101  0.63  211101  0.71  211110 
Gampaha  0.40  011111  0.56  011SOH  0.67  011SOH  0.78  011SOH 
Hambantota  0.31  010101  0.47  110101  0.60  210101  0.71  210101 
Jaffna  0.42  010011  0.58  012111  0.74  012011  0.82  012SOH 
Kalutara  0.54  112100  0.72  011000  0.79  110000  0.79  110000 
Kandy  0.33  012101  0.43  012101  0.48  112SOH  0.51  212SOH 
Kegalle  0.37  010SOH  0.55  211011  0.66  211SOH  0.75  211SOH 
Kilinochchi  0.51  010101  0.95  010101  2.13  111010  2.13  010002 
Kurunegala  0.25  011011  0.41  010011  0.53  011011  0.63  011011 
Mannar  1.16  011100  0.97  012101  1.10  112100  1.18  111101 
Matale  0.37  110101  0.53  110101  0.62  212011  0.70  112011 
Matara  0.35  212101  0.40  011101  0.46  212101  0.49  0110111 
Moneragala  0.29  110100  0.40  011100  0.48  210100  0.56  011100 
Mullaitivu  1.03  111100  1.70  112000  2.00  110000  2.58  111SOH 
Nuwara Eliya  0.48  212111  0.58  212101  0.66  212101  0.68  111000 
Polonnaruwa  0.32  111101  0.47  012101  0.57  111011  0.66  111011 
Puttalam  0.35  010101  0.46  010101  0.60  212101  0.72  010101 
Ratnapura  0.30  011111  0.43  012111  0.50  210111  0.57  112111 
Trincomalee  0.53  112000  0.79  010100  1.05  010100  1.15  112111 
Vavuniya  1.22  012000  1.43  012101  1.41  211101  1.48  012101 
Mean absolute relative error of out of series prediction at forecasting horizons of 1 to 4 months ahead for districts in Sri Lanka for Holt Winters models.
District  Horizon 1  Horizon 2  Horizon 3  Horizon 4  

Model  H  HW  H  HW  H  HW  H  HW 
Ampara  0.43  0.39  0.65  0.52  0.83  0.63  0.86  0.67 
Anuradhapura  0.34  0.22  0.66  0.35  0.99  0.45  1.22  0.53 
Badulla  0.46  0.54  0.67  0.75  0.87  0.95  0.84  0.96 
Batticaloa  0.41  0.41  0.65  0.65  0.82  0.82  0.97  0.97 
Colombo  0.35  0.37  0.39  0.43  0.44  0.48  0.46  0.53 
Galle  0.50  0.61  0.59  0.74  0.67  0.83  0.79  0.96 
Gampaha  0.43  0.43  0.59  0.59  0.70  0.70  0.78  0.78 
Hambantota  0.36  0.36  0.57  0.56  0.76  0.73  0.88  0.87 
Jaffna  0.43  0.46  0.62  0.63  0.79  0.85  0.85  0.97 
Kalutara  0.55  0.61  0.72  0.80  0.81  0.91  0.88  0.97 
Kandy  0.37  0.37  0.50  0.50  0.56  0.57  0.57  0.57 
Kegalle  0.39  0.40  0.63  0.62  0.83  0.82  0.94  0.95 
Kilinochchi  0.58  0.60  1.08  1.12  2.50  2.26  2.70  2.17 
Kurunegala  0.34  0.26  0.61  0.43  0.76  0.57  0.85  0.70 
Mannar  1.41  1.57  1.74  1.98  1.61  2.63  1.78  2.28 
Matale  0.45  0.41  0.73  0.63  0.96  0.74  1.13  0.81 
Matara  0.37  0.35  0.42  0.40  0.49  0.48  0.52  0.52 
Moneragala  0.31  0.31  0.42  0.41  0.54  0.52  0.62  0.63 
Mullaitivu  1.08  1.19  1.73  1.70  2.21  2.54  2.73  2.38 
Nuwara Eliya  0.49  0.50  0.61  0.60  0.69  0.69  0.69  0.69 
Polonnaruwa  0.37  0.37  0.60  0.60  0.76  0.76  0.82  0.82 
Puttalam  0.42  0.37  0.67  0.49  0.88  0.64  1.00  0.76 
Ratnapura  0.36  0.31  0.55  0.47  0.64  0.56  0.74  0.66 
Trincomalee  0.53  0.56  0.82  0.75  1.15  0.97  1.35  1.07 
Vavuniya  1.89  2.02  2.82  3.93  2.45  14.21  2.19  4.11 
In the analysis of covariates for the mean term, only the (S)ARIMA models shown in Table 1 were tested. Only for the districts Mannar and Ampara, inclusion of malaria in neighbouring districts lowered one month ahead mare, with 6.8% and 4.6%, respectively. For many other districts, inclusion of malaria in neighbouring districts raised the mare.
Districts in Sri Lanka for which inclusion of a covariate in the mean term of the best (S)ARIMA model tested improved the mean absolute relative error of out of series prediction at forecasting horizons of 1 to 4 months ahead.
District  Horizon (months)  Lag (months)  covariate  Improvement (%) 

Badulla  4  4  rainy day index, with a separate coefficient for each calendar month  6.5 
Gampaha  3  4  logarithmically transformed total monthly rainfall (mm)  3.8 
Gampaha  4  4  logarithmically transformed total monthly rainfall (mm)  4.5 
Mannar  1  2  logarithmically transformed total monthly rainfall (mm)  5.2 
Moneragala  2  2  monthly rainfall factored into quintiles  4.1 
Moneragala  2  3  rainy day index  4.6 
Moneragala  3  3  rainy day index  3.2 
Mullaitivu  1  1  monthly rainfall factored into quintiles  2.6 
logarithmically transformed total monthly rainfall (mm), with a separate  
Ratnapura  3  4  coefficient for each calendar month  3.9 
logarithmically transformed total monthly rainfall (mm), with a separate  
Ratnapura  4  4  coefficient for each calendar month  3.6 
logarithmically transformed total monthly rainfall (mm), with a separate  
Trincomalee  2  2  coefficient for each calendar month  8.4 
logarithmically transformed total monthly rainfall (mm), with a separate  
Trincomalee  3  3  coefficient for each calendar month  9.2 
Vavuniya  4  4  logarithmically transformed total monthly rainfall (mm)  2.5 
Discussion
Models without extrinsic explanatory variables
The mean absolute relative prediction error calculated by the best model (without extrinsic explanatory variables) tested was quite large for many districts. However, as the models were fitted to only half of the length of the timeseries available for the purpose of model testing (out of sample predictions are required), it is expected that for application in a forecasting system where the full series are used for fitting, the error will be reduced. For some districts in the north, the forecasting error was particularly large. For these districts, a relatively large proportion of the data had been imputed, and the quality of the existing data is likely compromised by the armed conflict in this region. General issues related to data quality are discussed elsewhere [23]. In this (primarily) temporal study, issues relating to spatial variation in data quality (e.g. through access to health facilities for sampling) are of less importance than those pertaining to temporal aspects, such as the deployment of mobile clinics during specific periods. Despite the sometimes large prediction errors, especially for larger forecasting horizons, prediction intervals yielded by these models (albeit less accurate for low predicted mean counts due to the Gaussian approximation used) could aid the AMC in assessing the risk of malaria in the near future, and adjust resources for preparedness accordingly. Although the best model selected varied among districts and over forecasting horizons, the difference between models was often small. Instead of specifying a different model for each situation, for practical implementation, it may be worth selecting for each district (or even group of districts) one model that performs well on average over a range of forecasting horizons (and districts within the group), provided that the prediction quality does not deteriorate more than a set percentage. A pilot forecasting system using district specific SARIMA models is currently being tested by the AMC in Sri Lanka (the system currently uses models without explanatory variables because a system to incorporate newly observed data is not yet in place). As the spatial resolution of the forecasting models presented is at district level, predictions will not help spatially targeted control at sub district level. For this, regional malaria control officers will have to rely on their experience of where within the district cases tend to occur if they occur, possibly aided by existing malaria maps at sub district level [23].
Models including rainfall as explanatory variable
It should be kept in mind that the malaria count data are not a direct proxy of new malaria infections or even infective bites. Recrudescent and relapsing cases (mostly due to ineffective drugs) occur multiple times in the malaria dataset, and immunity may play a role during periods of higher endemicity, thus weakening explanatory power of a variable such as rainfall, which would probably be better at explaining infectious bites [24].
Rainfall improved the prediction for eight districts, at one or more of the tested forecasting horizons, but it also worsened the prediction for other districts at various horizons. For some districts, the rainfall preceding malaria by two months improved performance at forecasting horizons of three and four months (not shown), but this is of little use in a forecasting system, unless rainfall can be predicted with high confidence (one to two months ahead). Although only tested for four districts, the rainy day index was promising as it improved results for two out of these.
The results of the analysis incorporating rainfall was remarkably different from what would be expected based on results of cross correlation analysis of malaria and rainfall. Although both (prewhitened) cross correlations [25] and the improvements of rainfall to prediction accuracy were generally low, (prewhitened) cross correlation analysis indicated that prediction accuracy for a number of districts in the centrewest and centresouth of the country was likely to benefit from rainfall (with a single, negative coefficient), and the present analysis found such improvement only for Gampaha District.
Varying seasonal effects of rainfall on malaria in seasonal interannual analysis [25] suggested that especially for districts in the north and east, prediction models would benefit from addition of rainfall with a monthly varying coefficient. However, only for the districts Trincomalee and Ratnapura (the latter situated in the south), this was the case. It is possible that for most of the districts, the training time series was too short (sixteen years) to estimate each of the twelve coefficients reliably.
For most districts (except the districts Mannar, Mullaitivu and Vavuniya), presumably due to strong short term temporal auto correlation, the observed number of malaria cases is a good predictor at a one month forecasting horizon (Figure 2). Interestingly, for Mannar and Mullaitivu, rainfall could improve predictions somewhat at this horizon. For the remaining six districts for which rainfall was found to improve predictions, this was mostly at larger forecasting horizons. For prediction with an even further forecasting horizon, use of predicted rainfall might be feasible. Rainfall could be predicted up to several months ahead using, for instance, the El Niño southern oscillation index, which in itself has proven to have a statistically significant relationship with malaria epidemics in the pre control era [6]. During periods when case reporting might be compromised (e.g. through civil war), rainfall may gain in relative importance as a predictor of the true number of cases, although this would be difficult to validate. It should be noted that high cross correlations between (not prewhitened, seasonal) malaria time series and extrinsic covariates (with seasonality) such as rainfall and temperature may exist [25], and these covariates may perform well in models that do not include fixed seasonal or autoregressive seasonal terms, but not necessarily better than models that do include fixed seasonal or autoregressive seasonal terms.
The contribution of rainfall to reducing the prediction error was modest, and it is arguable whether or not the achieved reduction in the prediction error (for instance, a reduction of 9.2%, bringing the mean relative error down from 1.05 to 0.95 at a horizon of three months in the district Trincomalee) merits investing in a system where at the end of each month, monitored rainfall data are collected and processed to obtain average values for the district surface for entering into the prediction model. However, as such data become increasingly available with the development of monthly rainfall data monitoring systems at district and sub district scale [26], the reduction in prediction error gained might well outweigh the (reduced) effort.
The modest improvement found by including rainfall compares well to a study in Ethiopia [17]. This study also found modest improvement (a reduction of 10.7% in the number of one step ahead predictions that were more than twice or less than half the observed value) by a model incorporating rainfall and temperature over a simple ARIMA(0,1,0) model that uses the previous value as predictor. However, the improvement would probably have been less if it had been tested on out of sample predictions. It is interesting to note that in this same paper, Abeku and colleagues [17] found that the ARIMA(0,1,0) performed better than the seasonal adjustment method (which performed unsatisfactorily on Sri Lankan data), whereas previously the seasonal adjustment method had been reported as superior [16]. Another study carried out in Ethiopia found that a prediction model including rainfall, temperature and cases in the previous month performed well in flagging potential epidemics as compared to observed cases, but was not compared with a prediction model based on past cases alone [13], therefore, the relative improvement cannot be assessed and compared to the improvement found in the present study.
Some explanatory variables not considered in this study and suggestions for future work
Other rainfall related variables such as soil moisture content and river flow might give better results than observed rainfall, as these are more directly related to malaria vector breeding conditions. The main malaria vector in Sri Lanka, Anopheles culicificacies, primarily breeds in pooling rivers (although there are also other habitats such as those mentioned above). In general, rainfall and river flow show strong cross correlations, and therefore rainfall can serve as a proxy for river flow. However, under dryer conditions important for vector breeding direct runoff will be decreased and river flow will be increasingly influenced by other hydrological processes such as percolation and evapotranspiration. As river flow and soil moisture are difficult to measure over large surfaces (and long term data with good spatial resolution are not readily available), they can be estimated through modelling, although rainfall will remain an important variable in such models [27]. Vegetation indices such as the normalized difference vegetation index (NDVI) were not studied because it can be argued that in a primarily temporal analysis, observed station rainfall is more closely related to breeding conditions than temporal changes in NDVI. Furthermore, remote sensing images of Sri Lanka suffer from obstruction by cloud cover during the monsoons. Apart from rainfall and rainfall related variables, another variable that is expected to have a strong temporal effect on malaria is vector control. This variable was not taken into account due to incomplete data. The effect of rainfall on malaria could be studied for data in the precontrol era [6], but with the reality of control measures being carried out this will be of little use for current prediction. The primary goal of this study was to develop an easy to use practical prediction model with the data available. The effect of missing important variables in a prediction model will not invalidate results, but will be expressed in larger prediction intervals. Nevertheless, inclusion of a malaria control variable, at least for those districts with relatively complete data, merits investigation.
Temperature was not considered as part of the present analysis, based on the assumption that it was of less importance than rainfall, showing little temporal variability (because Sri Lanka is situated close to the equator), and a large part of its temporal variability being governed by rainfall. Except for the hill country (covering largely the districts Nuwara Eliya, Kandy and Badulla), the temperature is generally conducive to malaria transmission throughout the year. However, for parts of the districts Kandy and Badulla, temperature could be limiting during part of (but not the whole of) the year and its role in these districts merits further investigation. In a study on the relationship between malaria and rainfall and temperature in Ethiopia, rainfall was found to be important in hot districts which were situated below 1650 m, but not in cold districts above 1650 m, where minimum temperature was significant [28]. Other environmental factors that are often considered in malaria studies are altitude and land use. Altitude was not taken into account because it does not fluctuate over time, and is thus of no use for temporal forecasting. Land use databases with monthly temporal resolution were not available. The performance of rainfall over several lag times accumulated, or at thresholds, remains to be explored. It is tempting to try to build a spacetime malaria forecasting model for the whole of Sri Lanka with more statistical power than a separate model for each district. Such a model should allow for regionally varying functions of covariates and take into account spatial auto correlation between districts or even MOH areas. For the purpose of a forecasting system, with the presently small malaria counts in most districts, it might be more appropriate to model the malaria counts directly following a negative binomial distribution, rather than through a logarithmic transformation [29]. Although easy to implement (and used in this work as well as work by others), the Gaussian (Normal) approximation of the malaria count data (after logarithmic transformation) is likely to affect the accuracy of the predictions, particularly when the counts are expected to be close to zero. Most importantly, this may yield inaccurate prediction intervals during periods of low case numbers. Although not so important in the current study (where models were evaluated on the means of the predictions), prediction intervals are very important for control planning.
Declarations
Acknowledgements
The author acknowledges the Directorate of the AMC and Regional Malaria Officers and their teams for making surveillance data available, and Dr W. van der Hoek for initiating the study. OJTB is funded through the NOAA, NSF, EPA and EPRI Joint Program on Climate Variability and Human Health.
Authors’ Affiliations
References
 Konradsen F, Amerasinghe FP, Hoek Van der W, Amerasinghe PH: Malaria in Sri Lanka: Current knowledge on transmission and control. 2000, Colombo: International Water Management InstituteGoogle Scholar
 Briet OJ, Galappaththy GN, Amerasinghe PH, Konradsen F: Malaria in Sri Lanka: one year posttsunami. Malar J. 2006, 5: 4210.1186/14752875542.PubMed CentralView ArticlePubMedGoogle Scholar
 Rajakaruna RS, Alifrangis M, Briët OJT, Galappaththy GNL, Amerasinghe PH, Konradsen F: Current situation of malaria and antimalarial drug resistance in Sri Lanka. Ceylon J Sci.Google Scholar
 Gunawardena DM, Wickremasinghe AR, Muthuwatta L, Weerasingha S, Rajakaruna J, Senanayaka T, Kotta PK, Attanayake N, Carter R, Mendis KN: Malaria risk factors in an endemic region of Sri Lanka, and the impact and cost implications of risk factorbased interventions. Am J Trop Med Hyg. 1998, 58: 533542.PubMedGoogle Scholar
 Abeysekera T, Wickremasinghe AR, Gunawardena DM, Mendis KN: Optimizing the malaria data recording system through a study of case detection and treatment in Sri Lanka. Trop Med Int Health. 1997, 2: 10571067. 10.1046/j.13653156.1997.d01183.x.View ArticlePubMedGoogle Scholar
 Bouma MJ, Kaay Van der HJ: The El Nino Southern Oscillation and the historic malaria epidemics on the Indian subcontinent and Sri Lanka: an early warning system for future epidemics?. Trop Med Int Health. 1996, 1: 8696. 10.1046/j.13653156.1996.d017.x.View ArticlePubMedGoogle Scholar
 Githeko AK, Lindsay SW, Confalonieri UE, Patz JA: Climate change and vectorborne diseases: a regional analysis. Bull World Health Organ. 2000, 78: 11361147.PubMed CentralPubMedGoogle Scholar
 Hoek Van der W, Konradsen F, Perera D, Amerasinghe PH, Amerasinghe FP: Correlation between rainfall and malaria in the dry zone of Sri Lanka. Ann Trop Med Parasitol. 1997, 91: 945949. 10.1080/00034989760347.View ArticlePubMedGoogle Scholar
 Basher R, Cane MA: Climate Variability, Climate Change and Malaria. The contextual determinants of malaria. Edited by: Casman E, Dowlatabadi H. 2002, Washing, DC.: Resources for the Future Press, 189215.Google Scholar
 Krishnamurti TN, Chakraborti A, Mehta VM, Mehta AV: Experimental prediction of climaterelated malaria incidence. 2007, [http://www.pitt.edu/~super2/2901130001/29021.ppt]Google Scholar
 GroverKopec EK, Blumenthal MB, Ceccato P, Dinku T, Omumbo JA, Connor SJ: Webbased climate information resources for malaria control in Africa. Malar J. 2006, 5: 3810.1186/14752875538.PubMed CentralView ArticlePubMedGoogle Scholar
 Meskel TG: Personal communication. 2007Google Scholar
 Teklehaimanot HD, Schwartz J, Teklehaimanot A, Lipsitch M: Weatherbased prediction of Plasmodium falciparum malaria in epidemicprone regions of Ethiopia II. Weatherbased prediction systems perform comparably to early detection systems in identifying times for interventions. Malar J. 2004, 19: 4410.1186/14752875344.View ArticleGoogle Scholar
 Thomson MC, DoblasReyes FJ, Mason SJ, Hagedorn R, Connor SJ, Phindela T, Morse AP, Palmer TN: Malaria early warnings based on seasonal climate forecasts from multimodel ensembles. Nature. 2006, 439: 576579. 10.1038/nature04503.View ArticlePubMedGoogle Scholar
 Myers MF, Rogers DJ, Cox J, Flahault A, Hay SI: Forecasting disease risk for increased epidemic preparedness in public health. Adv Parasitol. 2000, 47: 309330.PubMed CentralView ArticlePubMedGoogle Scholar
 Abeku TA, De Vlas SJ, Borsboom G, Teklehaimanot A, Kebede A, Olana D, van Oortmarssen GJ, Habbema JD: Forecasting malaria incidence from historical morbidity patterns in epidemicprone areas of Ethiopia: a simple seasonal adjustment method performs best. Trop Med Int Health. 2002, 7: 851857. 10.1046/j.13653156.2002.00924.x.View ArticlePubMedGoogle Scholar
 Abeku TA, De Vlas SJ, Borsboom GJ, Tadege A, Gebreyesus Y, Gebreyohannes H, Alamirew D, Seifu A, Nagelkerke NJ, Habbema JD: Effects of meteorological factors on epidemic malaria in Ethiopia: a statistical modelling approach based on theoretical reasoning. Parasitology. 2004, 128: 585593. 10.1017/S0031182004005013.View ArticlePubMedGoogle Scholar
 Craig MH, Kleinschmidt I, Nawn JB, Le Sueur D, Sharp BL: Exploring 30 years of malaria case data in KwaZuluNatal, South Africa: part I. The impact of climatic factors. Trop Med Int Health. 2004, 9: 12471257. 10.1111/j.13653156.2004.01340.x.View ArticlePubMedGoogle Scholar
 Ribeiro PJ, Diggle PJ: geoR: A package for geostatistical analysis. RNews. 2001, 1:Google Scholar
 Chatfield C: The analysis of time series: an introduction. 2004, Boca Raton: Chapman & Hall/CRCGoogle Scholar
 Burman JP, Otto MC: Outliers in time series. 1988, Bureau of the census statistical reseach division report series SRD Research Report Number: CENSUS/SRD/RR88114. Washington D.CGoogle Scholar
 Mwaniki KJ, Odhiambo OR, Charles W: Seasonal time series data imputation: comparison between feedforward neural networks and parametric approaches. East Afr J Stat. 2005, 1: 6883.Google Scholar
 Briët OJT, Gunawardena DM, Hoek Van der W, Amerasinghe FP: Sri Lanka malaria maps. Malar J. 2003, 2: 2210.1186/14752875222.PubMed CentralView ArticlePubMedGoogle Scholar
 Mabaso ML, Smith T: Empirical modelling and mapping of seasonality of malaria transmission by Anopheles gambiae sensu lato in Africa. UnpublishedGoogle Scholar
 Briët OJT, Vounatsou P, Gunawardena DM, Galappaththy GNL, Amerasinghe PH: Temporal correlation between malaria and rainfall in Sri Lanka. Malar J . 2008, 7: 77PubMed CentralView ArticlePubMedGoogle Scholar
 Zubair L: Personal communication. 2007Google Scholar
 Mahanama S, Koster R, Zubair L, Riehl R: On the predictability of seasonal streamflow with a Land Surface Model: Water and energy budget studies for Sri Lanka. UnpublishedGoogle Scholar
 Teklehaimanot HD, Lipsitch M, Teklehaimanot A, Schwartz J: Weatherbased prediction of Plasmodium falciparum malaria in epidemicprone regions of Ethiopia I. Patterns of lagged weather effects reflect biological mechanisms. Malar J. 2004, 3: 4110.1186/14752875341.PubMed CentralView ArticlePubMedGoogle Scholar
 Briët OJT, Vounatsou P, Amerasinghe PH: Generalized (S)ARIMA models for count data with application to malaria time series. UnpublishedGoogle Scholar
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