- Open Access
Spatiotemporal clusters of malaria cases at village level, northwest Ethiopia
Malaria Journalvolume 13, Article number: 223 (2014)
Malaria attacks are not evenly distributed in space and time. In highland areas with low endemicity, malaria transmission is highly variable and malaria acquisition risk for individuals is unevenly distributed even within a neighbourhood. Characterizing the spatiotemporal distribution of malaria cases in high-altitude villages is necessary to prioritize the risk areas and facilitate interventions.
Spatial scan statistics using the Bernoulli method were employed to identify spatial and temporal clusters of malaria in high-altitude villages. Daily malaria data were collected, using a passive surveillance system, from patients visiting local health facilities. Georeference data were collected at villages using hand-held global positioning system devices and linked to patient data. Bernoulli model using Bayesian approaches and Marcov Chain Monte Carlo (MCMC) methods were used to identify the effects of factors on spatial clusters of malaria cases. The deviance information criterion (DIC) was used to assess the goodness-of-fit of the different models. The smaller the DIC, the better the model fit.
Malaria cases were clustered in both space and time in high-altitude villages. Spatial scan statistics identified a total of 56 spatial clusters of malaria in high-altitude villages. Of these, 39 were the most likely clusters (LLR = 15.62, p < 0.00001) and 17 were secondary clusters (LLR = 7.05, p < 0.03). The significant most likely temporal malaria clusters were detected between August and December (LLR = 17.87, p < 0.001). Travel away home, males and age above 15 years had statistically significant effect on malaria clusters at high-altitude villages.
The study identified spatial clusters of malaria cases occurring at high elevation villages within the district. A patient who travelled away from home to a malaria-endemic area might be the most probable source of malaria infection in a high-altitude village. Malaria interventions in high altitude villages should address factors associated with malaria clustering.
Malaria transmission varies in space and time[1, 2]. It is a multifactorial disease and the aetiological agent has a complex life cycle requiring an insect vector, and the attribution of trends to specific factors remains difficult because of multiple drivers, including micro-ecology, utilization of interventions, demographic and population movement, drug resistance, land-use change, and access to health facilities[4, 5].
In highland areas with low endemicity, malaria transmission is highly variable and malaria acquisition risk for individuals is unevenly distributed even within a neighbourhood[6–8]. Many studies have been conducted to understand the spatiotemporal variation of malaria at areas below 2,000 m above sea level[9–14]. However, information about the spatiotemporal variation of malaria transmission risks in villages at altitude above 2,000 m is limited and poorly understood. As malaria transmission declines, understanding the heterogeneity in malaria transmission becomes crucial and creates opportunities for targeting interventions, while better methods are required in the field and in modelling. Understanding heterogeneity should focus on individuals who contribute disproportionately to malaria transmission and other driving factors. Such targeted interventions are supremely important tools in malaria elimination efforts.
Recent studies employing a combination of geographical information systems (GIS)[13, 16], scan statistics[17–19] and Bayesian modelling[20–22] have proven helpful in characterizing the spatial patterns of malaria and in determining linkages between spatial patterns and driving factors for malaria transmission risk. Improved understanding of spatiotemporal clustering of malaria in villages would be indispensable for government and malaria control and prevention partners to provide appropriate malaria interventions and resource allocation.
The aims of this study were to describe the spatial and temporal patterns of malaria transmission and identify drivers of the spatiotemporal patterns of malaria risk in high-altitude villages of northwest Ethiopia in an area of very low transmission intensity. The findings presented here have the potential to enhance the effectiveness of the national malaria control programme.
Study area and settings
The study was conducted in Dabat district, which is a predominantly rural area with a population of 159,091. The area of the district is 1,187.93 sq km, and 133.9 population density (Figure 1). The peak malaria transmission season in the study area is from September to December. Most malaria cases are due to Plasmodium falciparum infection.
Sample size determination
Stat Calc module of Epi Info™ 18.104.22.168 software was used to compute the sample size with an assumption of 95% level of confidence, 80% power, odds ratio of 1.63, ratio of control to cases 2:1, and assuming that 6.9% of the controls travelled in the previous month. A total of 1,934 (645 cases and 1,289 controls) was the planned sample size. During the actual data collection, a total of 1,644 patients (645 cases and 999 controls) were included in the study.
All patients who visited local health centres seeking treatment and who were permanent residents in the study district were included in the study. Patients who came from other districts were not included in the study. Daily malaria data were collected using passive surveillance system from patients who visited four local health facilities in the district from August 2012 to May 2013 (about 40 weeks). The data were collected by trained laboratory technicians working at each health facility laboratory unit, and were tested for malaria at the laboratory department.
A malaria case was defined as an individual from the study area who presented to the health facilities with malaria-like symptoms (fever, chills, severe malaise, headache; vomiting for children) and diagnosed either by microscopy, or rapid diagnostic test and microscopy together. Those patients who were negative for microscopy or rapid diagnostic test were regarded as patients without malaria.
Georeference coordinates were collected at village level using hand-held global positioning system (GPS). The kebeles (the lowest local administrative units) were also georeferenced with GPS. Each case and control was georeferenced to the location of the village in which the patient resided. A shape file with kebele and district boundaries and polygon shapes were obtained from the Central Statistical Agency of Ethiopia (CSA) and each kebele was georeferenced to its geographic centroid. The patients’ addresses and data were crosslinked with kebeles and villages using the Arc GIS 10 software. After completing the address and data crosslinked to villages and kebeles, each patient village and kebele was characterized by unique latitude and longitude location coordinates.
Individual information was collected using a pretested and structured questionnaire. The questionnaire comprised socio-economic characteristics, malaria preventive measures (insecticide-treated nets (ITNs) use, indoor residual spray (IRS)), and history of travel in the month preceding the interview, travel place, and the homestead surroundings.
SaTScan™ software, version 9.1 using the Kulldorf method was used to for cluster analysis. The discrete Bernoulli model[17, 27], was used to analyse the spatial and temporal patterns of malaria transmission. The number of cases in each location had Bernoulli distribution and the model requires data with or without a disease. Patients with malaria were taken as cases and patients who were negative for malaria were taken as controls to fit the Bernoulli model for the purpose of this study. The binomial data were analysed with the purely temporal and spatial scan statistics.
Spatial scan statistics were used to explore the spatial pattern of malaria cases, used to test hypotheses relating to the processes that may have given rise to the observed distributions, and used to identify significant spatial clusters of malaria cases at village level. SaTScan software used a circular window moved systematically throughout the study area to identify significant clustering of malaria cases and centred on each of a number of possible locations throughout the study villages and for each location. Cluster analysis was performed with the default maximum spatial cluster size of <50% of the population and again with a smaller maximum cluster size of <25% to look for possible subclusters. Fifty per cent was specified as the upper limit, which allowed both small and large clusters to be detected and ignored clusters that contained more than 50% of the population. Likelihood ratio test was used to test the hypothesis that there were elevated malaria cases compared with the distribution outside the moving window. The window sizes and locations with the maximum likelihood were defined as the most likely cluster(s). Monte Carlo replications of the dataset determined the distribution and p-value of the most likely and secondary clusters. The aim was to detect villages with high numbers of malaria cases. A standard of ‘no geographical overlap’ was used to report secondary clusters. The P-value was created using a combination of standard Monte Carlo, sequential Monte Carlo and Gumbel approximation and used 999 replications of Monte Carlo.
The malaria data were collected from patients seeking treatment at four local health facilities. These are typical Bernoulli data and modelled via logistic regression using Bayesian framework to identify the individual level factors. Let Y ij and p ij are the status and probability of P. falciparum or Plasmodium vivax infection, respectively, of all age patients j in village i. Assuming Y ij has a Bernoulli distribution, Y ij < Bernoulli(p ij ) and modelled covariates X ij and village-specific random effect Φi on the logit(pij), that is logit(pij) = XTijβ + Φi, where β is the vector of regression coefficients.
Markov chain Monte Carlo simulation was used to estimate the model parameters using Gibbs sampling. Two chain samplers with a burn in of 5,000 iterations were used. The deviance information criterion (DIC) was used to assess the goodness-of-fit of the full and reduced models where the smaller DIC value was considered as the better model fit. The analysis was done using the Bayesian statistical software WinBUGS version 1.4.1 (MRC Biostatistics Unit, Cambridge, UK).
The protocol was approved by the University of Gondar Ethical Review Committees (IRB). Verbal and written consent was obtained from all patients. In the case of illiterate patients, thumb-printed consent was obtained after consent was read by trusted literates. Study procedures and purposes were explained to parents/guardians; their understanding was confirmed through an interview before written or thumb-printed consent was obtained. Interviews were completely voluntary and all data were kept confidential.
Spatial distribution of malaria
A total of 1,644 patients presented with and without malaria. Of these, 645 cases of malaria were captured at the health facilities during the study period. Some 405 (62.8%) patients were diagnosed using microscopy and 240 (37.2%) of these diagnosed using rapid diagnostic test. Plasmodium falciparum, 355 (55.0%), was the higher species found, followed by P. vivax, 173 (26.8%), and all types, 117 (18.2%). Out of 645 malaria cases, 488 (75.7%) were from villages above 2,000 m above sea level, 66 (10.2%) were from villages between 1,750 and 2,000 m above sea level and 91 (14.1%) were from villages between 1,500 and 1,750 m above sea level.
The most likely spatial clusters were detected in high-altitude kebeles: Janbelew, Tenseye, Doka, Defiya, Doromamaye, Wekentown, Talakmesk, Abetera, and Weken Zurya (LLR = 16.23, p < 0.001). These clusters accounted for 263 (40.8%) of malaria cases (Figure 2). The secondary clusters were found at kebeles: Carbita, Dara, and Benker (LLR = 4.58, p < 0.04) and accounted for 147 (22.8%) of malaria cases (Figure 3). Patients who travelled away from home to malaria-endemic areas were high in kebeles where malaria cases were found clustered.
Spatial scan statistics identified a total of 56 (the most likely and secondary) spatial clusters of malaria at village level. Of these, 39 villages were the most likely clusters (LLR = 15.62, p < 0.00001) and 17 villages were secondary clusters (LLR = 7.05, p < 0.03). The most likely spatial clusters of malaria identified in villages were from the same kebeles where malaria cases were spatially clustered (Figure 4). It means that the most likely clustered villages were within the most likely spatial clustered kebeles. Villages identified within spatial most likely clusters were located at altitudes above 2,000 m compared with villages outside the cluster and accounted for 302 (46.8%) of the malaria cases. The secondary clusters accounted for 113 (17.5%) of the total malaria cases and clustered in the villages located between 1,500 and 2,000 m highland fringes, which are prone to malaria epidemics (Figure 3).
Temporal distribution of malaria
Of the total number of malaria cases, 384 (59.5%) were observed between September and December 2012. The peak months were November 110 (17.1%), October 107 (16.9%), and December 97 (15.0%). The majority, 354 (54.9%), of malaria infection was due to P. falciparum infections. September, October, November was the months of high malaria transmission. The peak weeks of malaria transmission were in November (week 2 and 4), and in October (week 3 and 4), and in December (week 2 and 4) (Figure 1).
Temporal scan statistics identified temporal clusters in all villages. The significant temporal clusters of malaria cases were from 1 August 2012 to 31 December 2012 (LLR = 17.874624, p < 0.001), followed by from 1 January 2013 to 28 February 2013 (LLR = 4.282231, p < 0.01). The secondary temporal clusters were found from 1 January 2013 to 28 February 2013 (LLR = 4.282231, p < 0.018).
Factors associated with malaria clusters
Based on the DIC value, the full model was considered the best model. Travel away home, 95% credible interval (0.737; 4.154), males, 95% credible interval (0.8416; 4.829) and age above 15 years, 95% credible interval (0.061; 0.123) had statistically significant effect on malaria clusters at high-altitude villages (zero is not included in the 95% credible interval) (Table 1).
In this study, malaria transmission showed spatiotemporal clusters in high-altitude villages. Travel away home, males and age above 15 years had statistically significant effect on malaria spatiotemporal clusters in high-altitude villages.
The spatial cluster analysis identified high-risk villages in high altitudes. The most likely spatial clusters of malaria cases were detected in villages and kebeles located above 2,000 m above sea level. This may be due to health facilities being located in high altitudes and which are easily reached by patients who lived in high-altitude villages and patients who lived closer to low and mid-highlands may not easily get to these health facilities to seek malaria treatment. Further, the patients who travelled away from home to low-lying areas where malaria is endemic might be most probable to bring malaria infection to high-altitude villages. Peripheries of health facilities closer to low and mid-highlands had not malaria diagnosis and laboratory personnel. The secondary spatial clusters were found in villages and kebeles located between 1,500 and 2,000 m. Studies reported that the occurrence of malaria epidemics and transmission above 2,000 m[10, 31], between 1,500 and 2,000 m[32, 33] above sea level. The increased number of malaria cases in these altitudes may be attributed to the presence of elevated transmission effective vectors, or to the environment favouring breeding for the vectors. Other reasons may be due to the hilly geography of the villages where the people live on top of hills and move to lower altitudes for their agricultural activities.
The study indicated that the space distribution of malaria is closely related to the topography of the environment. Unusual weather conditions of rainfall and temperatures[27, 34] may favour malaria transmission in the area. Malaria prevention and control strategies have not yet prioritized in these areas. In these areas, the people immunity is naïve and they are vulnerable to malaria epidemics. It is believed that the risk of malaria in the study villages may be closely related to the behaviour of villagers working and resting without protection, and mobility to lowland areas where malaria transmission is high. This shows that it is important to understand the spatial distribution of malaria at a finer geographic scale in high-altitude villages.
The majority of malaria cases occurred during September and December with peaks during November and accounted for the high proportion of total cases. The finding was consistent with another study. The temporal variations may be related to variations in meteorological parameters and could be utilized to effectively predict the incidence of malaria in high-altitude villages.
On the basis of this study, malaria transmission risks are in high-altitude villages located above 2,000 m. A patient who travels away from home to low-lying areas where malaria is endemic might have the most probable effect on malaria spatiotemporal patterns in high-altitude villages. Travel often increases exposure to infectious disease and can affect disease prevention and control efforts. Travel has also contributed to the global spread of malaria during the history of humankind. Non-immune individuals travelling from high, malaria-free altitudes to low-lying, malaria-endemic areas are predominantly susceptible to malaria infections if exposed to an infected mosquito, particularly in areas with high levels of transmission, and need to be educated about avoiding mosquito and other insect bites by using adequate preventive measures (ITNs and insect repellents).
The study focused on patients presenting at local health facilities during ten months, from August 2012 to May 2013, using a passive case detection method. This may be limited in showing the true picture of malaria at household and village level. The study was not sensitive to the locations of health facilities outside the study area; patients in certain kebeles and villages who sought care for malaria at facilities in adjacent districts would not be reflected in the dataset. Nevertheless, the passive case detection hinted at active case detection and identification of risk factors that cause spatiotemporal patterns of malaria risks in high-altitude villages. In addition, there is a loss of resolution by aggregating individual level data (obtained from health facilities) to the village level.
SaTScan and GIS-based spatial statistical techniques could provide an opportunity to clarify and identify malaria transmission risks within high-altitude villages, and help future investigations into environmental, climate and other factors responsible for increased malaria risks in high-altitude villages. The geographic visualization of malaria case distribution using these tools could help to understand malaria risk at village and kebele level and target interventions in high-risk areas.
In this study, only the associations between human population density/distribution and malaria cases in space-time and altitude were studied. Further studies to investigate the underlying causes of increased risk in the identified areas are recommended, including vector densities and distribution, vector infectivity, environmental and climatic factors, to have a more inclusive view of the malaria risk.
The study identified spatial and temporal clusters of malaria in high altitudes villages located above 2,000 m. A patient who travels away from home to malaria-endemic areas might have the most effect on malaria clusters in high-altitude villages. These results provide further insights into identifying the true picture of malaria clusters and causes at villages and enable the efficient and timely spatial targeting of preventive and control measures against the disease in high altitudes villages where people have low immunity.
Yeshiwondim AK, Gopal S, Hailemariam AT, Dengela DO, Patel HP: Spatial analysis of malaria incidence at the village level in areas with unstable transmission in Ethiopia. Int J Health Geogr. 2009, 8: 5-
Alemu K, Worku A, Berhane Y: Malaria Infection has spatial, temporal, and spatiotemporal heterogeneity in unstable malaria transmission areas in Northwest Ethiopia. PLoS One. 2013, 8: e79966-doi:101371/journalpone007996
Yukich JO, Taylor C, Eisele TP, Reithinger R, Nauhassenay H, Berhane Y, Keating J: Travel history and malaria infection risk in a low-transmission setting in Ethiopia: a case control study. Malar J. 2013, 12: 33-
Shanks GD, Hay SI, Omumbo JA, Snow RW: Malaria in Kenya’s Western Highlands. Emerg Infect Dis. 2005, 11: 1425-1432.
Lindbland KA, Walker ED, Onapa AW, Katungu J, Wilson ML: Land use change alerts malaria transmission parameters modifying temperature in highland area of Uganda. Trop Med Int Health. 2000, 5: 263-274.
Ghebreyesus TA, Haile M, Witten KH, Getachew A, Yohannes M, Lindsay SW, Byass P: Household risk factors for malaria among children in the Ethiopian highlands. Trans R Soc Trop Med Hyg. 2000, 94: 17-21.
Creasey A, Giha H, Hamad AA, El Hassan IM, Theander TG, Arnot DE: Eleven years of malaria surveillance in a Sudanese village highlights unexpected variation in individual disease susceptibility and outbreak severity. Parasitology. 2004, 129: 263-271.
Carter R, Mendis KN, Roberts D: Spatial targeting of interventions against malaria. Bull World Health Organ. 2000, 78: 1401-1411.
Woyessa A, Deressa W, Ali A, Lindtjørn B: Malaria risk factors in Butajira area, south-central Ethiopia: a multilevel analysis. Malar J. 2013, 12: 273-
Tesfaye S, Belyhun Y, Teklu T, Mengesha T, Petros B: Malaria prevalence pattern observed in the highland fringe of Butajira, Southern Ethiopia: A longitudinal study from parasitological and entomological survey. Malar J. 2011, 10: 153-
Haque U, Huda M, Hossain A, Ahmed SM, Moniruzzaman M, Haque R: Spatial malaria epidemiology in Bangladeshi highlands. Malar J. 2009, 8: 185-
Peterson I, Borrell LN, El-Sadr W, Teklehaimanot A: Individual and household level factors associated with malaria incidence in a highland region of Ethiopia: A Multilevel Analysis. Am J Trop Med Hyg. 2009, 80: 103-111.
Kreuels B, Kobbe R, Adjei S, Kreuzberg C, Reden CV, Bäter K, Klug S, Busch W, Adjei O, May J: Spatial variation of malaria incidence in young children from a geographically homogeneous area with high endemicity. J Infect Dis. 2008, 197: 85-89.
Wimberly MC, Midekisa A, Semuniguse P, Teka H, Henebry GM, Chuang T-W, Senay GB: Spatial synchrony of malaria outbreaks in a highland region of Ethiopia. Trop Med Int Health. 2012, 17: 1192-1201.
World Health Organization: Global malaria control and elimination: report of a technical review. 2008, Geneva: WorldHealth Organization, http://www.who.int/malaria/publications/en/ atoz/9789241596756/en/. Accessed 15 May 2014
Dogana HM, Cetin I, Egri M: Spatiotemporal change and ecological modelling of malaria in Turkey by means of geographic information systems. Trans R Soc Trop Med Hyg. 2010, 104: 726-732.
Cheung W, Senay GB, Singh A: Trends and spatial distribution of annual and seasonal rainfall in Ethiopia. Int J Climatol. 2008, 10: 1002-
Teklehaimanot HD, Schwartz J, Teklehaimanot A, Lipsitch M: Weather-based prediction of Plasmodium falciparum malaria in epidemic-prone regions of Ethiopia II. Malar J. 2004, 3: 44-doi:101186/1475-2875-3-44
Ethiopia national malaria indicator survey 2011. 2012, Available at http://www.unicef.org/ethiopia/ET_MIS_2011_Report.pdf. Accessed 2013 November 12
Gosoniu L, Vounatsou P, Sogoba N, Smith T: Bayesian modelling of geostatistical malaria risk data. Geospatial Health. 2006, 1: 127-139.
Zayeri F, Salehi M, Pirhosseini H: Geographical mapping and Bayesian spatial modeling of malaria incidence in Sistan and Baluchistan province, Iran. Asian Pacific J Trop Med. 2011, 4: 985-992.
Zacarias OP, Andersson M: Spatial and temporal patterns of malaria incidence in Mozambique. Malar J. 2011, 10: 189-
CSA: Ethiopian central statistical ageny.http://www.csa.gov.et/index.php/2013-02-20-13-43-35/national-statistics-abstract,
Malaria indicator survey 2011. 2012, Available at http://www.unicef.org/ethiopia/ET_MIS_2011_Report.pdf. Accessed 2013 November 12
ESRI 2011. ArcGIS Desktop: Release 10. Redlands, CA, USA: Environmental Systems Research Institute,http://www.esri.com/software/arcgis/,
Kulldorff M: SaTScan User Guide for version 9.0. available at http://www.satscan.org/download.html 2010
Abeku T, van Oortmarssen GJ, Borsboom G, de Vlas SJ, Habbema JDF: Spatial and temporal variations of malaria epidemic risk in Ethiopia: factors involved and implications. Acta Trop. 2003, 87: 331-340.
Beck-Wörner C, Raso G, Vounatsou P, N’goran EK, Rigo G, Parlow E, Utzinger J: Bayesian spatial risk prediction of Schistosoma Mansoni infection in Western Côte D’ivoire using a remotely-sensed digital elevation model. Am J Trop Med Hyg. 2007, 76: 956-963.
Gelfand AE, Smith AFM: Sampling-based approaches to calculating marginal densities. J Am Stat Assoc. 1990, 85: 398-409.
Spiegelhalter DJ, Best NG, Carlin BP, Linde AVD: Bayesian measures of model complexity and fit. J R Stat Soc Ser B Stat Methodol. 2002, 64: 583-616.
Fontaine RE, Najjar AE, Prince JS: The 1958 malaria epidemic in Ethiopia. Am J Trop Med Hyg. 1961, 10: 795-803.
Negash K, Kebede A, Medhin A, Argaw D, Babaniyi O, Guintran J, Delacollette C: Malaria epidemics in the highlands of Ethiopia. East Afr Med J. 2005, 82: 186-192.
Checchi F, Cox J, Balkan S, Tamrat A, Priotto G, Alberti KP, Zurovac D, Guthmann JP: Malaria Epidemics and Interventions, Kenya, Burundi, Southern Sudan, and Ethiopia, 1999–2004. Emerg Infect Dis. 2006, 12: 1477-1485.
Siraj AS, Santos-Vega M, Bouma MJ, Yadeta D, Carrascal DR, Pascual M: Altitudinal changes in malaria incidence in highlands of Ethiopia and Colombia. Science. 2014, 343: 1154-
Federal Minstry of Health: National Malaria Guidelines. 2012, Federal ministry of health: Addis Ababa, Ethiopia, 3
Galvani AP, May RM: Epidemiology: dimensions of super spreading. Nature. 2005, 438: 293-295.
Schlagenhauf P: Malaria: from prehistory to present. Infect Dis Clin N Am. 2004, 18: 189-205.
The authors gratefully acknowledge support received from University of Gondar and Addis Continental Institutes of Public Health for providing fund. We are also grateful to Dabat District Health department and health centre heads for facilitating the field work. We thank the Ethiopian Central Statistics Agency for providing us with the shape files for the study area.
The authors declare that they have no competing interests.
Conception and design of the work, acquisition of data, analysis and interpretation of data was done by KA, AW and YB. Drafting the article, revising it critically for intellectual content, and final approval of the version to be published was done by KA, AW and YB. All authors read and approved the final manuscript.