Mapping Malaria Risk in India between 2019-2023: A Tool for the Public to Track Malaria

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Mapping Malaria Risk in India between 2019-2023: A Tool for the Public to Track Malaria | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Article Mapping Malaria Risk in India between 2019-2023: A Tool for the Public to Track Malaria Harish Phuleria, Avik Sam, Neha Keshri, Ipsita Bhowmick, Anupkumar Anvikar This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-6781302/v1 This work is licensed under a CC BY 4.0 License Status: Posted Version 1 posted You are reading this latest preprint version Abstract With less than two years remaining from 2027 – the year which the government has targeted to achieve zero Indigenous cases, we map the malaria indicators across the 700+ districts for five years between 2019 and 2023 using spatiotemporal maps and also assess the potential drivers of malaria transmission in different regions. We used the annual district-wise malaria data from the National Center for Vector Borne Disease Control Programme (NCVBDC) and the cross-sectional socio-economic data from the National Family Health Survey. We also collated the meteorological and land-use land-cover data from the MERRA-2 and Sentinel-LPA satellites, respectively. We then developed region-specific ensembles of spatiotemporal models that allowed us to identify the associated covariates while the regions were identified using the Getis-Ord Gi* statistics. With 0.33 million malaria cases in 2019, the COVID-19 pandemic led to a significant reduction in reported cases. The P. falciparum affected regions are widespread in North-eastern and Central India. However, after the pandemic, an emerging geographical expansion into the north-eastern parts is observed for the P. vivax , which is evident from the clusters and the spatiotemporal ensemble models. Population belonging to scheduled castes and scheduled tribes and those economically marginalised are among the most vulnerable, but lifestyle habits such as drinking water practices, maternal education, and healthcare accessibility are identified as the potential drivers of malaria transmission. We also developed a digital dashboard that allows the general public and the stakeholders to track the malaria indicators for each district and the corresponding year. Health sciences/Diseases/Infectious diseases/Malaria Health sciences/Health care/Health policy Health sciences/Health care/Public health/Epidemiology Health sciences/Health care/Disease prevention/Lifestyle modification Malaria Mapping Digital dashboard MIDAS Socio-economic inequities Policy Figures Figure 1 Figure 2 Figure 3 Figure 4 Figure 5 1. Introduction Malaria has significantly impacted India's healthcare infrastructure due to its high incidences (Kumari et al., 2022 ; Rahi & Sharma, 2022 ; Sam et al., 2024 ). Recently, the World Malaria Report 2024 estimated 249 million malaria cases that disproportionately affect the most marginalised population, highlighting equitable access to life-saving tools as the key to reversing malaria trends (World Health Organisation, 2024). Further, the World Health Organisation's recently formulated "Global Malaria Programme Operational Strategy for 2024–2030" identified country ownership and accessibility to resilient health systems as well as data-driven decision-making as the road ahead for malaria elimination (World Health Organization, 2024 ). Previously, a need for a holistic framework for data dissemination and a synergistic multilateral framework involving academic, public and private sector involvement was highlighted as a significant targeted measure that could play a pivotal role in India's journey against Malaria (Sam et al., 2024 ). Malaria risk mapping has been proved useful in Africa, where usage of malaria cartography reemerged in the late 1990s, which also coincided with activities aimed at intensive control and elimination (Odhiambo et al., 2020 ; Snow et al., 1996 ; Snow & Noor, 2015 ). Additionally, there has been a gigantic shift towards the usage of modern statistical methods in developing spatiotemporally detailed maps that are being increasingly applied in informing policies (Kraemer et al., 2016 ; Ye & Andrada, 2020 ). Spatiotemporal modelling techniques for a comprehensive quantification of malaria burden and research-based insights into the key contributing factors are recommended as an epidemiological prerequisite to intervention strategies (Odhiambo et al., 2020 ; Wimberly et al., 2021 ). Previously, in India, geospatial mapping reported that 13% of the country is under very high malaria risks, with a high probability of outbreaks in low to moderate-risk regions (S. Sarkar et al., 2019 ). Further, mapping techniques have been used in surveying the vectors and insecticidal resistance in India (Kumar et al., 2024 ; A. Sarkar et al., 2020 ; Singh et al., 2017 ). Through this work, we first identify the spatiotemporal trends in the malaria parameters from 2019 to 2023 and understand the spatial clusters using maps for all malaria epidemiological parameters. We used an ensemble of Random Forest Regression and Zero-Inflated Poisson Regression to assess the significant covariates that could influence malaria transmission in the three-primary malaria-predominant regions. We then develop a dashboard that visualises the spatial trends and clusters for the general public and the country's stakeholders. 2. Methods 2.1 Malaria Data District-level data on the malaria situation for the year 2018-2023 were obtained from the NCVBDC, a Ministry of Health and Family Welfare, Government of India department responsible for the control of malaria in India. The parameters included Percentage of Falciparum Cases (% PF), Annual Parasite Incidence (API), Annual Falciparum Incidence (AFI), Annual Blood Slide Examination Rate (ABER), Slide Positivity Rate (SPR), and Slide Falciparum Rate (SFR). More information about these parameters is discussed in Sam et al., 2025 (Under Review). Further, the Annual Vivax Incidence (AVI) was estimated by subtracting the AFI from API. 2.2 Spatial Analysis For the spatial plots, we used the official shapefiles available on the Online Maps Portal, maintained by the Ministry of Science & Technology (Ministry of Space & Technology, 2025) . We accessed the official government websites for those districts that were mismatched and standardised the district names to ensure consistency with the available malaria data. This step was essential for accurately mapping and plotting the data. Through this, we retrieved 667 districts in 2019, 674 in 2020, 682 in both 2021 and 2022, and 678 in 2023. We then plotted the spatial distribution for each malaria parameter using Geopandas v.0.14.3 (Bossche et al., 2025). The spatial clusters were identified using the Getis-Ord Gi* statistic, which is suitable for comparing the global mean of all districts with the local mean of each district and the corresponding neighbouring districts. Districts having standardised z-scores > 0 and p-values < 0.05 were classified as the hotspots where spatial clustering exists. The Getis-Ord Gi* statistic and their methods have been discussed in detail here (Getis & Ord, 1992; Sam et al., 2025) . 2.3 Meteorological, socio-economic and Land-use Land-cover covariates The meteorological data was collated from the Modern-Era Retrospective Analysis for Research and Applications version 2, or MERRA-2, which provides monthly advanced reanalysis data at a spatial resolution of 0.5°×0.625° (Gelaro et al., 2017). We collated the monthly gridded data on surface temperature, precipitation, specific humidity and soil moisture that was overlaid on the district boundaries, for obtaining the district-wise data. This was then aggregated at the annual level to obtain the mean, maximum and minimum for each variable. Data on the land-use land-cover classes were collated from the ESA Sentinel-2 imagery that provided the data at a 10m resolution (Karra et al., 2021). Using the same procedure of overlaying the data, we obtained the areas for water bodies, tree cover, bare lands, built-up areas, snow land, croplands and flooded vegetation for all districts and each year. For the socio-economic data, we used the Household Recode File from the representative National Family Health Survey-5 conducted between 2019-2021 to obtain district-wise household-related information describing the socio-economic characteristics, healthcare choices, nutritional and educational status, and prevalence of common disorders. 2.4 Ensemble models We first identified three distinct regions that have witnessed the highest degree of transmission observed between 2019 and 2023. The clusters that were identified using the Getis-Ord G* statistics, as discussed in 2.2, also belonged to these three regions. The 'Central' regions comprised Telangana, Maharashtra, Chhattisgarh, Odisha and Andhra Pradesh, while the 'North' region consisted of Uttar Pradesh and Uttarakhand. The seven states in north-eastern India, namely Assam, Arunachal Pradesh, Meghalaya, Nagaland, Tripura, Mizoram and Manipur, comprised the 'North-eastern' region. We then used an ensemble modelling approach where ensembles of Random Forest Regression Models were developed for each year and region to obtain the feature importance for ranking the variables according to their importance. For obtaining the ranked matrices of the most significant variables, a Monte Carlo Simulation was performed, following which we developed three spatiotemporal Zero-inflated Poisson (ZIP) Regression models for the central, northeast and northern regions of the country separately, as a significant number of districts reported zero API. More information about the methodology can be found in Sam et al., 2025. In contrast to our previous methodology, we here computed the API per 100,000 people to convert all decimals to integers as required for the ZIP, while no categorical variable for mapping the P. falciparum distribution was introduced. In contrast, we introduced a categorical variable corresponding to the year, accounting for the temporal variations. The spatiotemporal model can be written as: where i denotes the states and t represents the year. For the present study, the Risk Ratios (RR) and the Odds Ratios (OR) were computed by exponentiating the model coefficients for the Poisson and logistic components in the ZIP model, respectively. 2.5 Creation of the 'MIDAS' Dashboard We created an interactive dashboard showing the spatiotemporal variations in the malaria parameters. We used a GeoJSON file to load the geospatial data onto the dashboard. The dashboard was developed using the Dash and Plotly (Plotly Technologies Inc, 2015) frameworks available in Python. Previously, the NIMR-MDB dashboard was developed using R but is currently not hosted for viewing by the general public (C. P. Yadav & Sharma, 2022) . We also used data analytical software like Pandas (Reback et al., 2020) and GeoPandas (Jordahl et al., 2019). Our dashboard was structured into three sections to enhance user experience and effective data exploration. The interactive control panel on the left includes dropdown menus and radio buttons that can be used to filter the data by year, geographical regions (states and districts), and malaria indicators that are of interest. The visualisation area on the right shows the spatial and temporal visualisations, where trends and distributions of malaria incidences are depicted. The third section is the header and footer, which sets a context for the general user. For the visualisation components, we have used choropleth maps and time-series maps that track the indicators over time using interactive illustrations. We name our dashboard "MIDAS", or the Malaria Indicators Dashboard for Analysis and Surveillance. The dashboard has been successfully tested on an internal server and will be made publicly accessible after requisite approvals. 3. Results and Discussion 3.1 Spatiotemporal variations in the malaria parameters across India India reported a cumulative of 0.33 million cases in 2019, which dropped to 0.18 million in 2020 - the year of the COVID-19 pandemic. There was a 13.3% reduction in the cases in 2021, but it increased by 9% in 2022 and again by 29% in 2023 when compared to the previous year. The temporal trends for the Blood Slides Collected (BSC) and Examined (BSE), Rapid Diagnostic Kits (RDT) Collected and Examined, and the Total Number of P. falciparum (Pf t ) and P. vivax (Pv t ) cases are provided in Table S1. There was a similar drop in the total blood slides collected and examined from 2019 to 2020, which later started improving from 2021 onwards. However, the SPR marginally increased from 0.252 in 2019 to 0.254 in 2020, which later dropped to 0.18 in 2021 and 0.17 in 2023. Both SFR and % PF were higher than the corresponding Slide Vivax Rate and % P. vivax from 2020 onwards (Sam et al., 2024). Among the states, Maharashtra had the highest blood slides examined in 2019; however, the neighbouring state of Gujarat reported the highest ABER (24.5), with districts like the Dangs (44.57) and Kachchh (40.29) reporting higher surveillance. In 2019, a P. vivax outbreak in the densely populated districts of Bareilly (34576) and Budaun (18302) in Uttar Pradesh reported the highest proportion (35.4%) of P. vivax in the whole country. Subsequently, both of these districts had SPR> 10. Further, the P. falciparum (% PF > 85) predominant districts of Sukma, Bijapur, Dakshin Bastar Dantewada and Narayanpur in Chhattisgarh, and Lawngtlai, Mamit and Lunglei in Mizoram reported SPR> 5 and API > 15. Interestingly, Nuh in Haryana, which was majorly affected by P. falciparum (84.7%), reported a high SPR of 5.77 but an API of 0.68 and an ABER of 1.18. In 2020, the same districts in Chhattisgarh and the north-eastern states, along with Malkangiri in Odisha, reported both API and AFI > 10. Gadchiroli in Maharashtra, which borders Bastar to the east, reported a higher API of 7.7 when compared to 2019 (2.09). It was among the districts having the highest surveillance with an ABER of 75.37. In the subsequent years, Gadchiroli reported an API of 10.47 in 2021, 7.79 in 2022 and 5 in 2023, while the SPR was also restricted to below 1. The eastern city of Kolkata, which is among the world's most densely populated metropolitan cities, has reported API > 2 since 2019, with a maximum of 5.9 in 2022. Except in 2021 (AFI = 1.5; % PF = 33.3), Kolkata reported AFI < 1, while the % PF varied between 5.5-14.5, highlighting the significance of P. vivax in the malaria transmission. We note that P. falciparum-predominant regions have consistently been the same throughout the years – it is primarily dominant in Central India and North-eastern India. Consequently, these are the regions that have reported very high API and AFI > 10. For instance, Lawngtlai in Mizoram has reported very high P. falciparum-based transmission for all five years, which was the maximum for the whole country in 2021 (API = 26.2; AFI = 22.4; SPR: 4.1), 2022 (API = 39.3; AFI = 30.3, SPR: 4.8) and in 2023 (API = 56.2; AFI = 38.9; SPR: 16.6). However, a transition to P. vivax was observed in Northeast India. A very high P. vivax transmission was observed in Lawngtlai, Mamit and Lunglei in Mizoram and Dhalai and South Tripura in Tripura. In Lawngtlai, there was a 213% increase in the AVI in 2020 when compared to 2019. The transmission further intensified in 2022 and 2023, as an AVI of 9.0 and 17.6 was reported in Lawngtai. A similar pattern was observed for the remaining districts (Figure 3), which also share international borders with Myanmar and Bangladesh. Previously, cross-boundary malaria was highlighted as a potential risk factor for malaria resurgence in the region (Kumari et al., 2022; Sam et al., 2024). The spatial distribution of API across the districts is provided in Figure 1, while the distribution of AVI is provided in the supplementary. 3.2 Identification of spatial clusters using Getis-Ord Gi* Statistics We classified the districts further based on their Getis-Ord Z-scores and the associated p-values. Districts with z-scores greater than 0 and p-values < 0.05 were classified as hotspots (Getis & Ord, 1992). We observe that the hotspots are distributed in the same districts only from 2019 to 2024. For API, these districts are distributed across two distinct regions in the country, namely the Central Region covering Maharashtra (1), Andhra Pradesh (4), Telangana (1), Chhattisgarh (6), and Odisha (2), and the Northeast Region spanning across Assam (2), Mizoram (8), and Tripura (8). An additional zone in the northern parts of the country that covers Uttar Pradesh and Uttarakhand was observed. The significant hotspots observed for (a) API, (b) AFI, and (c) AVI are provided in Figure 2, while the spatial maps and the intensity of the transmission are provided in Figure 3. For API, we observe that Bastar (Z-score: 4.95), Dastin Bastar Dantewada (Z-score: 4.71) and Sukma (Z-score: 4.5) in the Central Zone show highly significant clustering in 2019. The neighbouring districts of Narayanpur (Z-score: 3.0), Kondagaon (Z-score: 2.97) and Gadchiroli (Z-score: 2.47) are also identified as hotspots. We observe that these districts show a lesser extent of clustering over the years as their Z-scores reduce below 2 in 2023 (Figure 2). In contrast, the districts in northeast India, such as Saiha, Lawngtlai, Serchhip, Lunglei, Champai & Mamit, show increasing Z-scores, with the maximum in 2023. For instance, Saiha and Lunglei reported Z-scores of 4.87 and 4.78, respectively. The eight districts in Tripura also reported maximum Z-scores in 2023. Hailakandi in Assam and Kolasib in Mizoram emerged as hotspots in 2023. Further, the districts in Andhra Pradesh and Telangana were identified as hotspots in 2019 and 2020 only. Similar to the API, the significant hotspots for the AFI were restricted broadly to the central and northeast parts of the country. The districts in the central region exhibited very high clustering between 2019 and 2021, which declined slightly in 2022 and 2023. For instance, Bastar in Chhattisgarh reported a Z-score of 4.77 in 2019, which decreased to 3.76 in 2021 and 2.58 in 2023. The neighbouring districts of Sukma and Dakshin Bastar Dantewada in Chhattisgarh that reported very high Z-scores > 4 also followed a similar trend. In contrast, the clustering in north-eastern districts, especially those in Mizoram (Saiha, Serchhip, Lawngtlai and Champai), reported increased clustering in the later years as the Z-scores were > 4. The clustering in Tripura reported relatively moderate clustering with Z-scores ~ 2.1, which reduced in the later years. A few districts that reported very low transmission, such as Hailakandi in Assam, were also categorised as high-risk areas due to the neighbouring districts reporting very high API (Figure S5). We observe a geographical shift in the clusters observed for AVI that is also evident in the spatial distribution maps of AVI throughout the years (Figure S1; Section 3.1). All five districts that emerged as the focal point of AVI transmission, namely Lawngtlai, Mamit and Lunglei in Mizoram and Dhalai and South Tripura in Tripura, were all classified as hotspots for AVI. Thus, the emergence of P. vivax is occurring in this part of the country that was previously dominated by P. falciparum . In the north, the districts around Bareilly were identified as significant hotspots in 2019 and 2020, but the clustering was not significant in the subsequent years as these regions also witnessed fewer cases (Figure 1). Likewise, a similar trend was observed in the central region as districts like Sukma and Uttar Bastar Kanker, which are also categorised as significant hotspots for AFI, did not emerge as clusters for AVI post-2021. However, in contrast, the districts in north-eastern India showed very strong clustering after 2021. Districts in Mizoram, such as Saiha, Lawngtai, Lunglei and Serchhip, showed Z-scores > 5 in 2023 and > 4.5 in both 2022 and 2021, while all eight districts in Tripura were classified as significant hotspots with the highest degree of clustering in 2023. 3.3 Identifying potential risk factors for malaria transmission using the spatiotemporal ensemble model Using the region-specific ensemble of Random Forest Regression and Zero-inflated Poisson Regression models, the significant covariates that are likely influencing malaria transmission were identified for each of the parameters, i.e. API, AFI and AVI. The estimated region-wise associations or the Risk Ratios for API, AFI and AVI in districts reporting ≥ 0 are provided in Figure 4. We observe that for API in the Central Region, % total of Scheduled Castes and Scheduled Tribes (RR: 2.18 (95% CI: 2.1, 2.27)), % population not having mobile (RR: 1.7 (95% CI: 1.68, 1.73)) and % population who are not having normal BMI (RR: 1.06 (95% CI: 1.03, 1.08)) are among the socio-economic determinants positively associated with increased malaria transmission in districts. In our previous work, we found the same factors responsible for the malaria risk for the entire country (Sam et al., 2025; Under Review). Obesity has been previously identified as a risk factor in Sweden (Wyss et al., 2017), while malnutrition was associated with malaria in Cameroon (Kojom Foko et al., 2021). We also observe that % of households (HH) owning livestock is negatively associated with malaria in all regions for API (0.3 < RR < 0.7), but it is positively associated with AVI in the Central (RR: 1.3 (95% CI: 1.19, 1.42)). Livestock-based interventions have been recommended as a strategy for controlling malaria (Franco et al., 2014) , but the in-house raising of animals in Indonesia (Hasyim et al., 2018) and the presence of cattle in households in Tanzania were associated with malaria (Mayagaya et al., 2015) . Thus, more evidence-based research is needed to ascertain the role of livestock in malaria control. Similarly, a mother's education is negatively associated with API in all three regions, but we observe a positive association with AVI in the Central Region (RR: 1.7 (95% CI: 1.53, 1.88)). An educated mother will be aware of the symptoms of malaria. During outbreaks, testing and diagnosis increase due to pre-existing knowledge about the symptoms. This could lead to more cases being reported to the system. Similarly, in the absence of outbreaks, awareness about the prevention measures and careful adoption of the interventions will reduce the risk of malaria (Njau et al., 2014) . Healthcare accessibility, which is indicated by factors such as % of the population accessing treatment from private doctors or public hospitals, is negatively associated with the malaria risk for all regions and parameters. We also observe that % of HH having Rashtriya Swasthya Bima Yojana (RSBY) is positively associated with malaria parameters in multiple regions. The RSBY is a flagship programme of the Ministry of Health, Government of India that offers health insurance coverage to families below the poverty line. Economically marginalised households are more likely to access healthcare facilities due to their health insurance coverage (Thomas, 2016). In the north-eastern region, factors such as % HH living in muddy walled structures as well as % HH belonging to the poorest wealth index are positively associated with API, AFI and AVI. Economically disadvantaged communities are among the most vulnerable sections in this region, as earlier reported in Assam (K. Yadav et al., 2014). The percentage of HH using unprotected drinking water from sources like natural springs is also associated with the API (RR: 1.29 (95% CI: 1.28, 1.3)) and AFI (RR: 1.24 (95% CI: 1.23, 1.25)), as also reported in Ethiopia (Yang et al., 2020). Previously, these muddy houses have been linked to an increased risk of malaria in Mandla, India (Sharma et al., 2021). We also observe a significant positive association shown by % HH using Insecticide Treated Nets (ITNs) in the northeast with API (RR: 3.5 (95% CI: 3.36, 3.64)), AFI (RR: 2.27 (95% CI: 2.16, 2.39)) and AVI (RR: 3.45 (95% CI: 3.2, 3.71)). In contrast, the % HH using ITNs had a negative association with the API (RR: 0.15 (95% CI: 0.14, 0.17)) and AVI (RR: 0.26 (95% CI: 0.23, 0.29)) in the North Region. This implies that outdoor transmission could be responsible for the malaria outbreaks in the north-eastern region. Contrarily, only a few districts, such as Budaun, reported high transmission in the North, and they had a very low proportion (1.7%) of HHs using ITNs. Thus, with less ITN usage, it is likely that the cases increased during outbreaks. Additionally, in the north, we also observe that both % of the population using rainwater for drinking purposes and % of the population fetching water elsewhere for household usage (RR: 4.54 (95% CI: 4.19, 4.9)) are very strongly associated with the API. In Kolkata and Chennai, Anopheles Stephensi has reportedly been found in overhead water tanks, which had been kept open by residents to collect rainfall for later usage (Mandal et al., 2011). Thus, water storage practices in this northern belt could be responsible for the increased outbreaks. The 2018 outbreak in Bareilly, a district in Uttar Pradesh, was also attributed to excessive rainfall, along with poor surveillance (Kamal et al., 2020). Moreover, travelling to fetch water has been linked to increased cases in Africa (Ahmed et al., 2020; Minale & Alemu, 2018). In the northeast, we observe that % of HH having a water source in their own yard is also positively associated with the AVI (RR: 1.55 (95% CI: 1.42, 1.7)). In Tanzania, increasing coverage of non-piped water was associated with rising malaria cases (Shayo et al., 2021). Additionally, the prevalence of tobacco non-smokers was positively associated with malaria in the north. In Nigeria, decreased endophily for Anopheles was previously reported in a room that was habitated by smokers; however, the role of tobacco smoking habits needs to be investigated (Obembe et al., 2018). The forested land area defined by the 'Trees' variable was positively associated with API, AFI and AVI in both the Central and Northeast regions. This was complemented by the meteorological variables like the maximum of both precipitation and specific humidity. In the north, agricultural land defined by the LULC variable 'crops' was positively associated with both API and AVI. To investigate the temporal factor, the categorical variables' Year' for 2020, 2021, 2022 and 2023 were included with 2019 as the reference. We obtained a significant negative association for these variables with API, AFI and AVI for both the central and northern regions, reflecting a decrease in cases. However, a significant positive association was shown with API in 2023 and with AVI in 2020, 2021 and 2022 for the northeast region. Thus, our model could capture the increase in AVI in the north-eastern region, as also observed in Figure 2. The estimated ORs for the districts reporting API, AFI and AVI = 0 are provided in the supplementary. Overall, the models reported MSEs < 0.3 for AVI, between 0.15 and 2.6 for API and < 1.9 for AFI, thus indicating the suitability of the models. 3.4 Dashboard Our 'MIDAS' dashboard provides the spatiotemporal mapping of malaria indicators for all districts between 2019 and 2023. On the left panel, the user can choose between spatial and temporal variations. For both, there are dropdown menus through which a user can select the year and the parameters of interest. After initialisation, the spatial maps and temporal plots are generated. Using the mouse, the data for all districts can be viewed. The temporal maps provide the annual change in the malaria parameters for each district. The snapshot for the dashboard is provided in Figure 5, while the detailed Standard Operating Procedure is provided as supplementary material. 4. Conclusion Through this work, we map the spatiotemporal distributions of malaria indicators between 2019 and 2023. We observe that malaria has reduced in the last five years, compared to the previous decades, although there is a marginal increase in 2023 when compared to 2022. The significant hotspots for API, AVI and AFI are concentrated in Central India and North-eastern India; however, the clusters for AVI were also found in the northern states of Uttar Pradesh and Uttarakhand. A geographical expansion in the clusters for AVI is observed in Northeast India throughout the years. This unprecedented increase in P. vivax has been confirmed microscopically and molecularly at subcentre and village spatial levels (Unpublished Data). Our region-specific spatiotemporal models for each indicator suggest that while economically marginalised communities continue to be the most vulnerable sections, drinking water practices, maternal education, and healthcare accessibility are the likely drivers of the transmission. We believe that simple behavioural changes in the population, such as periodic overhead water tank cleaning or adopting ITNs and a healthy lifestyle, could reduce the malaria burden. Our dashboard is expected to raise awareness among the general public and help the stakeholders involved in malaria control in tracking the malaria indicators over the years. Our study uses annual data, where the true impact of seasonality can not be measured. Further, while the ecological study design is helpful in assessing the population-level patterns, the risks reported here should be reassessed through cross-sectional or longitudinal study designs to avoid potential bias, although similar associations have been reported elsewhere. We also recommend to the stakeholders to include the identified variables during data collection on reported malaria cases. Future work should also focus on longer temporal data to assess the impact of weather variables. We hope that our study will help the stakeholders and generate awareness among the general public of the country. Let's end malaria once and for all together! Declarations Funding: Funding for this study was provided by the Gates Foundation (NV-044445). AS wants to thank the Ministry of Education for providing the Prime Minister Research Fellowship (ID-1302077). Acknowledgements: The authors thank the National Centre for Vector Borne Disease Control Programme for the malaria data, the Indian Institute for Population Science and the Demographic and Health Survey for the National Family Health Survey data, and the National Aeronautics and Space Administration for the meteorological data. The authors thank Dr. Tanu Jain (Director, NCVBDC), Dr. Pranab Jyoti Bhuyan (Additional Director, NCVBDC) and the malaria team at the NCVBDC for their valuable insights. The work is based on research findings by the authors and not the opinion of the government. References Ahmed, S., Reithinger, R., Kaptoge, S. K., & Ngondi, J. M. (2020). Travel Is a Key Risk Factor for Malaria Transmission in Pre-Elimination Settings in Sub-Saharan Africa: A Review of the Literature and Meta-Analysis. The American Journal of Tropical Medicine and Hygiene , 103 (4), 1380. https://doi.org/10.4269/AJTMH.18-0456 Bossche, J. Van den, Jordahl, K., Fleischmann, M., Richards, M., McBride, J., Wasserman, J., Badaracco, A. G., Snow, A. D., Ward, B., Tratner, J., Gerard, J., Perry, M., cjqf, Hjelle, G. A., Taves, M., Hoeven, E. ter, Cochran, M., Bell, R., rraymondgh, … Gardiner, J. (n.d.). geopandas/geopandas: v1.0.1 . https://doi.org/10.5281/ZENODO.12625316 Franco, A. O., Gomes, M. G. M., Rowland, M., Coleman, P. G., & Davies, C. R. (2014). Controlling Malaria Using Livestock-Based Interventions: A One Health Approach. PLOS ONE , 9 (7), e101699. https://doi.org/10.1371/JOURNAL.PONE.0101699 Gelaro, R., McCarty, W., Suárez, M. J., Todling, R., Molod, A., Takacs, L., Randles, C. A., Darmenov, A., Bosilovich, M. G., Reichle, R., Wargan, K., Coy, L., Cullather, R., Draper, C., Akella, S., Buchard, V., Conaty, A., da Silva, A. M., Gu, W., … Zhao, B. (2017). The Modern-Era Retrospective Analysis for Research and Applications, Version 2 (MERRA-2). Journal of Climate , 30 (14), 5419–5454. https://doi.org/10.1175/JCLI-D-16-0758.1 Getis, A., & Ord, J. K. (1992). The Analysis of Spatial Association by Use of Distance Statistics. Geographical Analysis , 24 (3), 189–206. https://doi.org/10.1111/J.1538-4632.1992.TB00261.X Hasyim, H., Dhimal, M., Bauer, J., Montag, D., Groneberg, D. A., Kuch, U., & Müller, R. (2018). Does livestock protect from malaria or facilitate malaria prevalence? A cross-sectional study in endemic rural areas of Indonesia. Malaria Journal , 17 (1), 1–11. https://doi.org/10.1186/S12936-018-2447-6/TABLES/2 Jordahl, K., Van Den Bossche, J., Wasserman, J., McBride, J., Gerard, J., Tratner, J., Perry, M., & Farmer, C. (n.d.). geopandas/geopandas: v0.5.0. Zndo . https://doi.org/10.5281/ZENODO.2705946 Kamal, S., Chandra, R., Mittra, K. K., & Sharma, S. N. (2020). An investigation into outbreak of malaria in Bareilly district of Uttar Pradesh, India. Journal of Communicable Diseases , 52 (4), 1–11. https://doi.org/10.24321/0019.5138.202034 Karra, K., Kontgis, C., Statman-Weil, Z., Mazzariello, J. C., Mathis, M., & Brumby, S. P. (2021). GLOBAL LAND USE/LAND COVER WITH SENTINEL 2 AND DEEP LEARNING. International Geoscience and Remote Sensing Symposium (IGARSS) , 2021-July , 4704–4707. https://doi.org/10.1109/IGARSS47720.2021.9553499 Kojom Foko, L. P., Nolla, N. P., Nyabeyeu Nyabeyeu, H., Tonga, C., & Lehman, L. G. (2021). Prevalence, Patterns, and Determinants of Malaria and Malnutrition in Douala, Cameroon: A Cross-Sectional Community-Based Study. BioMed Research International , 2021 (1), 5553344. https://doi.org/10.1155/2021/5553344 Kraemer, M. U. G., Hay, S. I., Pigott, D. M., Smith, D. L., Wint, G. R. W., & Golding, N. (2016). Progress and Challenges in Infectious Disease Cartography. Trends in Parasitology , 32 (1), 19–29. https://doi.org/10.1016/J.PT.2015.09.006 Kumar, G., Gupta, S., Kaur, J., Pasi, S., Baharia, R., Mohanty, A. K., Goel, P., Sharma, A., & Rahi, M. (2024). Mapping malaria vectors and insecticide resistance in a high-endemic district of Haryana, India: implications for vector control strategies. Malaria Journal , 23 (1), 1–11. https://doi.org/10.1186/S12936-023-04797-8/TABLES/5 Kumari, R., Kumar, A., Dhingra, N., & Sharma, S. N. (2022). Transition of Malaria Control to Malaria Elimination in India. In Journal of Communicable Diseases (Vol. 54, Issue 1, pp. 124–140). Indian Society for Malaria and Communicable Diseases. https://doi.org/10.24321/0019.5138.202259 Mandal, B., Biswas, B., Banerjee, A., Mukherjee, T. K., Nandi, J., & Biswas, & D. (2011). Breeding propensity of Anopheles stephensi in chlorinated and rainwater containers in Kolkata City, India. J Vector Borne Dis , 48 , 58–60. www.mrcindia.org/chennai.hmt. Mayagaya, V. S., Nkwengulila, G., Lyimo, I. N., Kihonda, J., Mtambala, H., Ngonyani, H., Russell, T. L., & Ferguson, H. M. (2015). The impact of livestock on the abundance, resting behaviour and sporozoite rate of malaria vectors in southern Tanzania. Malaria Journal , 14 (1), 1–14. https://doi.org/10.1186/S12936-014-0536-8/TABLES/4 Minale, A. S., & Alemu, K. (2018). Mapping malaria risk using geographic information systems and remote sensing: The case of Bahir Dar City, Ethiopia. Geospatial Health , 13 (1), 157–163. https://doi.org/10.4081/gh.2018.660 Ministry of Space & Technology. (2025). Survey of India . https://onlinemaps.surveyofindia.gov.in/Digital_Product_Show.aspx Njau, J. D., Stephenson, R., Menon, M. P., Kachur, S. P., & McFarland, D. A. (2014). Investigating the Important Correlates of Maternal Education and Childhood Malaria Infections. The American Journal of Tropical Medicine and Hygiene , 91 (3), 509–519. https://doi.org/10.4269/AJTMH.13-0713 Obembe, A., Popoola, K. O. K., Oduola, A. O., & Awolola, S. T. (2018). Differential behaviour of endophilic Anopheles mosquitoes in rooms occupied by tobacco smokers and non-smokers in two Nigerian villages. Journal of Applied Sciences and Environmental Management , 22 (6), 981–985. https://doi.org/10.4314/JASEM.V22I6.23 Odhiambo, J. N., Kalinda, C., MacHaria, P. M., Snow, R. W., & Sartorius, B. (2020). Spatial and spatio-temporal methods for mapping malaria risk: a systematic review. BMJ Global Health , 5 (10), 2919. https://doi.org/10.1136/BMJGH-2020-002919 Plotly Technologies Inc. (2015). Collaborative data science . Plotly Technologies Inc. Rahi, M., & Sharma, A. (2022). Malaria control initiatives that have the potential to be gamechangers in India's quest for malaria elimination. The Lancet Regional Health - Southeast Asia , 2 , 100009. https://doi.org/10.1016/j.lansea.2022.04.005 Reback, J., McKinney, W., Jbrockmendel, Van Den Bossche, J., Augspurger, T., Cloud, P., Gfyoung, Sinhrks, Klein, A., Hawkins, S., Roeschke, M., Tratner, J., She, C., Ayd, W., Petersen, T., MomIsBestFriend, Garcia, M., Schendel, J., Hayden, A., … Winkel, M. (2020). pandas-dev/pandas: Pandas 1.0.5. Zndo . https://doi.org/10.5281/ZENODO.3898987 Sam, A. K., Karmakar, S., Mukhopadhyay, S., & Phuleria, H. C. (2024). A historical perspective of malaria policy and control in India. IJID Regions , 12 , 100428. https://doi.org/10.1016/J.IJREGI.2024.100428 Sarkar, A., Kumar, V., Jasrotia, A. S., Taloor, A. K., Kumar, R., Sharma, R., Khajuria, V., Raina, G., Kouser, B., & Roy, S. (2020). Spatial Analysis and Mapping of Malaria Risk in Dehradun City India: A Geospatial Technology-Based Decision-Making Tool for Planning and Management . 207–221. https://doi.org/10.1007/978-981-15-2097-6_14 Sarkar, S., Singh, P., Lingala, M. A. L., Verma, P., & Dhiman, R. C. (2019). Malaria risk map for India based on climate, ecology and geographical modelling. Geospatial Health , 14 (2), 281–292. https://doi.org/10.4081/gh.2019.767 Sharma, R. K., Rajvanshi, H., Bharti, P. K., Nisar, S., Jayswar, H., Mishra, A. K., Saha, K. B., Shukla, M. M., Das, A., Kaur, H., Wattal, S. L., & Lal, A. A. (2021). Socio-economic determinants of malaria in tribal dominated Mandla district enrolled in Malaria Elimination Demonstration Project in Madhya Pradesh. Malaria Journal , 20 (1), 1–13. https://doi.org/10.1186/S12936-020-03540-X/TABLES/4 Shayo, F. K., Nakamura, K., Al-Sobaihi, S., & Seino, K. (2021). Is the source of domestic water associated with the risk of malaria infection? Spatial variability and a mixed-effects multilevel analysis. International Journal of Infectious Diseases , 104 , 224–231. https://doi.org/10.1016/J.IJID.2020.12.062 Singh, P., Lingala, M. A. L., Sarkar, S., & Dhiman, R. C. (2017). Mapping of Malaria Vectors at District Level in India: Changing Scenario and Identified Gaps. Https://Home.Liebertpub.Com/Vbz , 17 (2), 91–98. https://doi.org/10.1089/VBZ.2016.2018 Snow, R. W., Marsh, K., & Le Sueur, D. (1996). The need for maps of transmission intensity to guide malaria control in Africa. Parasitology Today , 12 (12), 455–457. https://doi.org/10.1016/S0169-4758(96)30032-X Snow, R. W., & Noor, A. M. (2015). Malaria risk mapping in Africa The historical context to the Information for Malaria (INFORM) project . Thomas, T. K. (2016). Role of health insurance in enabling universal health coverage in India: A critical review. Health Services Management Research , 29 (4), 99–106. https://doi.org/10.1177/0951484816670191/ASSET/D98EA4BB-0994-4C0B-AE48-F95F055111DA/ASSETS/IMAGES/LARGE/10.1177_0951484816670191-FIG3.JPG Wimberly, M. C., de Beurs, K. M., Loboda, T. V., & Pan, W. K. (2021). Satellite Observations and Malaria: New Opportunities for Research and Applications. Trends in Parasitology , 37 (6), 525–537. https://doi.org/10.1016/J.PT.2021.03.003/ATTACHMENT/A6F80937-DD23-43E2-B10A-3606AAC53BB1/MMC1.DOCX World Health Organization. (2024). Global Malaria Programme operational strategy 2024-2030 . 01–84. World malaria report 2024 . (2024). World Health Organisation. https://www.who.int/teams/global-malaria-programme/reports/world-malaria-report-2024 Wyss, K., Wångdahl, A., Vesterlund, M., Hammar, U., Dashti, S., Naucler, P., & Färnert, A. (2017). Obesity and Diabetes as Risk Factors for Severe Plasmodium falciparum Malaria: Results From a Swedish Nationwide Study. Clinical Infectious Diseases , 65 (6), 949–958. https://doi.org/10.1093/CID/CIX437 Yadav, C. P., & Sharma, A. (2022). National Institute of Malaria Research-Malaria Dashboard (NIMR-MDB): A digital platform for analysis and visualisation of epidemiological data. The Lancet Regional Health - Southeast Asia , 5 . https://doi.org/10.1016/j.lansea.2022.100030 Yadav, K., Dhiman, S., Rabha, B., Saikia, P. K., & Veer, V. (2014). Socio-economic determinants for malaria transmission risk in an endemic primary health centre in Assam, India. Infectious Diseases of Poverty , 3 (1), 1–8. https://doi.org/10.1186/2049-9957-3-19/TABLES/3 Yang, D., He, Y., Wu, B., Deng, Y., Li, M., Yang, Q., Huang, L., Cao, Y., & Liu, Y. (2020). Drinking water and sanitation conditions are associated with the risk of malaria among children under five years old in sub-Saharan Africa: A logistic regression model analysis of national survey data. Journal of Advanced Research , 21 , 1–13. https://doi.org/10.1016/J.JARE.2019.09.001 Ye, Y., & Andrada, A. (2020). Estimating Malaria Incidence through Modeling Is a Good Academic Exercise, but How Practical Is It in High-Burden Settings? The American Journal of Tropical Medicine and Hygiene , 102 (4), 701–702. https://doi.org/10.4269/AJTMH.20-0120 Additional Declarations There is NO Competing Interest. Supplementary Files image1.png Graphical Abstract SupplementaryMalaria20192023mapping.docx Supplementary Material 1 Supplementary2MalariamappingSOPDashboard.docx Supplementary Material 2 Cite Share Download PDF Status: Posted Version 1 posted You are reading this latest preprint version Research Square lets you share your work early, gain feedback from the community, and start making changes to your manuscript prior to peer review in a journal. As a division of Research Square Company, we’re committed to making research communication faster, fairer, and more useful. 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Also discoverable on Platform About Our Team In Review Editorial Policies Advisory Board Help Center Resources Author Services Accessibility API Access RSS feed Manage Cookie Preferences © Research Square 2026 | ISSN 2693-5015 (online) Privacy Policy Terms of Service Do Not Sell My Personal Information {"props":{"pageProps":{"initialData":{"identity":"rs-6781302","acceptedTermsAndConditions":true,"allowDirectSubmit":true,"archivedVersions":[],"articleType":"Article","associatedPublications":[],"authors":[{"id":469322227,"identity":"34a1ef9a-af0e-42b4-bfb9-9e9e415fa95c","order_by":0,"name":"Harish Phuleria","email":"data:image/png;base64,iVBORw0KGgoAAAANSUhEUgAAAZAAAAAyAQMAAABI0h/eAAAABlBMVEX///8AAABVwtN+AAAACXBIWXMAAA7EAAAOxAGVKw4bAAAA0UlEQVRIiWNgGAWjYDACCQbGAyCSn5mxgRkswkxYCwNYi2QzY2MzKVoYGAwOMDA2E+Uuc+kegwMf91jIGx9nbn9cwGAnz8DOewCvFss5ZwwOzngmYbjtMNBhMxiSDRuY+RLwajG4kWNwmOeABCNYCw8DcwIDM48BYS1/DkjYb24Ga6knUgvDAYnEDcxgLYcJa7GckVZwsOeARPIMoMNmzzA4bthGSIu5RPLGBz8O1Nn29x9/8Lmgolqen/8MAYdhcNnwqsfUMgpGwSgYBaMACwAATR9BIltXuRsAAAAASUVORK5CYII=","orcid":"https://orcid.org/0000-0001-5801-0015","institution":"IIT Bombay","correspondingAuthor":true,"prefix":"","firstName":"Harish","middleName":"","lastName":"Phuleria","suffix":""},{"id":469322228,"identity":"04b9c1b5-71fc-4b0b-8b77-5cf76dc389b6","order_by":1,"name":"Avik Sam","email":"","orcid":"","institution":"Indian Institute of Technology Bombay, Mumbai, India","correspondingAuthor":false,"prefix":"","firstName":"Avik","middleName":"","lastName":"Sam","suffix":""},{"id":469322229,"identity":"23270e2d-28cc-498a-9763-e45d14a1af49","order_by":2,"name":"Neha Keshri","email":"","orcid":"","institution":"Indian Institute of Technology Bombay, Mumbai, India","correspondingAuthor":false,"prefix":"","firstName":"Neha","middleName":"","lastName":"Keshri","suffix":""},{"id":469322230,"identity":"a40a176b-9de8-4045-aad9-c31b6d8490a2","order_by":3,"name":"Ipsita Bhowmick","email":"","orcid":"","institution":"Regional Medical Research Center-Northeast Region (RMRC-NE)-ICMR","correspondingAuthor":false,"prefix":"","firstName":"Ipsita","middleName":"","lastName":"Bhowmick","suffix":""},{"id":469322231,"identity":"043ab45f-7f16-48a4-8a37-6cded71fe980","order_by":4,"name":"Anupkumar Anvikar","email":"","orcid":"","institution":"National Institute Malaria Research","correspondingAuthor":false,"prefix":"","firstName":"Anupkumar","middleName":"","lastName":"Anvikar","suffix":""}],"badges":[],"createdAt":"2025-05-30 05:45:13","currentVersionCode":1,"declarations":"","doi":"10.21203/rs.3.rs-6781302/v1","doiUrl":"https://doi.org/10.21203/rs.3.rs-6781302/v1","draftVersion":[],"editorialEvents":[],"editorialNote":"","failedWorkflow":false,"files":[{"id":88395715,"identity":"89e331c4-30c2-4d45-b199-c398708b56fb","added_by":"auto","created_at":"2025-08-06 06:00:57","extension":"png","order_by":1,"title":"Figure 1","display":"","copyAsset":false,"role":"figure","size":433458,"visible":true,"origin":"","legend":"\u003cp\u003eSpatiotemporal variations in API across India between 2019 and 2023. The color bar represents the API.\u003c/p\u003e","description":"","filename":"image2.png","url":"https://assets-eu.researchsquare.com/files/rs-6781302/v1/d747a9dd33ebf4f72b464f25.png"},{"id":88396297,"identity":"02eb110b-5984-4d4e-8891-0bd067c38b38","added_by":"auto","created_at":"2025-08-06 06:08:57","extension":"png","order_by":2,"title":"Figure 2","display":"","copyAsset":false,"role":"figure","size":763262,"visible":true,"origin":"","legend":"\u003cp\u003eSignificant hotspots observed for (a) API, (b) AFI and (c) AVI between 2019-2023. The red boxes indicate neighbouring clusters. The size of the scatter and the intensity of the colour correspond to the magnitude of the z-scores.\u003c/p\u003e","description":"","filename":"image3.png","url":"https://assets-eu.researchsquare.com/files/rs-6781302/v1/e128b855d84550570123a7fc.png"},{"id":88395719,"identity":"3ebf405f-c7b2-46e3-86ba-6855ca356c76","added_by":"auto","created_at":"2025-08-06 06:00:57","extension":"png","order_by":3,"title":"Figure 3","display":"","copyAsset":false,"role":"figure","size":463175,"visible":true,"origin":"","legend":"\u003cp\u003eSpatiotemporal distribution in (a) API, (b) AFI and (c) AVI in districts identified as part of the clusters. Few of the districts with zero API also fall in the high-risk zone (Figure 2) due to high malaria transmission observed in the neighbouring districts.\u003c/p\u003e","description":"","filename":"image4.png","url":"https://assets-eu.researchsquare.com/files/rs-6781302/v1/5448f67e056f589cb81b2660.png"},{"id":88395721,"identity":"75e0d7a1-ce3d-4124-aa27-46b570e02fb7","added_by":"auto","created_at":"2025-08-06 06:00:57","extension":"png","order_by":4,"title":"Figure 4","display":"","copyAsset":false,"role":"figure","size":743729,"visible":true,"origin":"","legend":"\u003cp\u003eEstimated associations (RRs) for API, AFI and AVI. In the north, the spatiotemporal model did not converge due to very low AFI reported.\u003c/p\u003e","description":"","filename":"image5.png","url":"https://assets-eu.researchsquare.com/files/rs-6781302/v1/eb1c8e882edca77c1d276bc7.png"},{"id":88395723,"identity":"0d30677e-aa40-4980-b55f-85dc8baab156","added_by":"auto","created_at":"2025-08-06 06:00:58","extension":"png","order_by":5,"title":"Figure 5","display":"","copyAsset":false,"role":"figure","size":651441,"visible":true,"origin":"","legend":"\u003cp\u003eScreenshot of the 'MIDAS' dashboard showing spatiotemporal changes in the malaria parameters.\u003c/p\u003e","description":"","filename":"image6.png","url":"https://assets-eu.researchsquare.com/files/rs-6781302/v1/d674ae864d2b3eab8eff9bcf.png"},{"id":88396372,"identity":"ba23f157-5a0c-4ef3-9542-7b412b956218","added_by":"auto","created_at":"2025-08-06 06:09:05","extension":"pdf","order_by":0,"title":"","display":"","copyAsset":false,"role":"manuscript-pdf","size":3353329,"visible":true,"origin":"","legend":"","description":"","filename":"manuscript.pdf","url":"https://assets-eu.researchsquare.com/files/rs-6781302/v1/92857d52-fafa-4606-b347-b20282e9a5ea.pdf"},{"id":88395722,"identity":"2fc17ce1-cc0b-4358-8e26-3fc3a54df83e","added_by":"auto","created_at":"2025-08-06 06:00:58","extension":"png","order_by":1,"title":"","display":"","copyAsset":false,"role":"supplement","size":361140,"visible":true,"origin":"","legend":"\u003cp\u003e\u003cstrong\u003eGraphical Abstract\u003c/strong\u003e\u003c/p\u003e","description":"","filename":"image1.png","url":"https://assets-eu.researchsquare.com/files/rs-6781302/v1/62d4a113c3fecaa89968380e.png"},{"id":88395725,"identity":"abff324f-a78f-4e7d-99a5-169a4972b116","added_by":"auto","created_at":"2025-08-06 06:00:58","extension":"docx","order_by":2,"title":"","display":"","copyAsset":false,"role":"supplement","size":4194936,"visible":true,"origin":"","legend":"\u003cp\u003eSupplementary Material 1\u003c/p\u003e","description":"","filename":"SupplementaryMalaria20192023mapping.docx","url":"https://assets-eu.researchsquare.com/files/rs-6781302/v1/3ca29133043189c9b828bfc0.docx"},{"id":88395720,"identity":"3f818996-4125-42ae-91d5-8c13d12a0a36","added_by":"auto","created_at":"2025-08-06 06:00:57","extension":"docx","order_by":3,"title":"","display":"","copyAsset":false,"role":"supplement","size":708320,"visible":true,"origin":"","legend":"\u003cp\u003eSupplementary Material 2\u003c/p\u003e","description":"","filename":"Supplementary2MalariamappingSOPDashboard.docx","url":"https://assets-eu.researchsquare.com/files/rs-6781302/v1/9491c7c498f77b34c194a170.docx"}],"financialInterests":"There is \u003cb\u003eNO\u003c/b\u003e Competing Interest.","formattedTitle":"Mapping Malaria Risk in India between 2019-2023: A Tool for the Public to Track Malaria","fulltext":[{"header":"1. Introduction","content":"\u003cp\u003eMalaria has significantly impacted India's healthcare infrastructure due to its high incidences (Kumari et al., \u003cspan citationid=\"CR13\" class=\"CitationRef\"\u003e2022\u003c/span\u003e; Rahi \u0026amp; Sharma, \u003cspan citationid=\"CR22\" class=\"CitationRef\"\u003e2022\u003c/span\u003e; Sam et al., \u003cspan citationid=\"CR24\" class=\"CitationRef\"\u003e2024\u003c/span\u003e). Recently, the World Malaria Report 2024 estimated 249\u0026nbsp;million malaria cases that disproportionately affect the most marginalised population, highlighting equitable access to life-saving tools as the key to reversing malaria trends (World Health Organisation, 2024). Further, the World Health Organisation's recently formulated \"Global Malaria Programme Operational Strategy for 2024\u0026ndash;2030\" identified country ownership and accessibility to resilient health systems as well as data-driven decision-making as the road ahead for malaria elimination (World Health Organization, \u003cspan citationid=\"CR34\" class=\"CitationRef\"\u003e2024\u003c/span\u003e). Previously, a need for a holistic framework for data dissemination and a synergistic multilateral framework involving academic, public and private sector involvement was highlighted as a significant targeted measure that could play a pivotal role in India's journey against Malaria (Sam et al., \u003cspan citationid=\"CR24\" class=\"CitationRef\"\u003e2024\u003c/span\u003e).\u003c/p\u003e \u003cp\u003eMalaria risk mapping has been proved useful in Africa, where usage of malaria cartography reemerged in the late 1990s, which also coincided with activities aimed at intensive control and elimination (Odhiambo et al., \u003cspan citationid=\"CR20\" class=\"CitationRef\"\u003e2020\u003c/span\u003e; Snow et al., \u003cspan citationid=\"CR30\" class=\"CitationRef\"\u003e1996\u003c/span\u003e; Snow \u0026amp; Noor, \u003cspan citationid=\"CR31\" class=\"CitationRef\"\u003e2015\u003c/span\u003e). Additionally, there has been a gigantic shift towards the usage of modern statistical methods in developing spatiotemporally detailed maps that are being increasingly applied in informing policies (Kraemer et al., \u003cspan citationid=\"CR11\" class=\"CitationRef\"\u003e2016\u003c/span\u003e; Ye \u0026amp; Andrada, \u003cspan citationid=\"CR40\" class=\"CitationRef\"\u003e2020\u003c/span\u003e). Spatiotemporal modelling techniques for a comprehensive quantification of malaria burden and research-based insights into the key contributing factors are recommended as an epidemiological prerequisite to intervention strategies (Odhiambo et al., \u003cspan citationid=\"CR20\" class=\"CitationRef\"\u003e2020\u003c/span\u003e; Wimberly et al., \u003cspan citationid=\"CR33\" class=\"CitationRef\"\u003e2021\u003c/span\u003e).\u003c/p\u003e \u003cp\u003ePreviously, in India, geospatial mapping reported that 13% of the country is under very high malaria risks, with a high probability of outbreaks in low to moderate-risk regions (S. Sarkar et al., \u003cspan citationid=\"CR26\" class=\"CitationRef\"\u003e2019\u003c/span\u003e). Further, mapping techniques have been used in surveying the vectors and insecticidal resistance in India (Kumar et al., \u003cspan citationid=\"CR12\" class=\"CitationRef\"\u003e2024\u003c/span\u003e; A. Sarkar et al., \u003cspan citationid=\"CR25\" class=\"CitationRef\"\u003e2020\u003c/span\u003e; Singh et al., \u003cspan citationid=\"CR29\" class=\"CitationRef\"\u003e2017\u003c/span\u003e). Through this work, we first identify the spatiotemporal trends in the malaria parameters from 2019 to 2023 and understand the spatial clusters using maps for all malaria epidemiological parameters. We used an ensemble of Random Forest Regression and Zero-Inflated Poisson Regression to assess the significant covariates that could influence malaria transmission in the three-primary malaria-predominant regions. We then develop a dashboard that visualises the spatial trends and clusters for the general public and the country's stakeholders.\u003c/p\u003e"},{"header":"2. Methods","content":"\u003ch2\u003e2.1\u0026nbsp;Malaria Data\u003c/h2\u003e\n\u003cp\u003eDistrict-level data on the malaria situation for the year 2018-2023 were obtained from the NCVBDC, a Ministry of Health and Family Welfare, Government of India department responsible for the control of malaria in India. The parameters included Percentage of Falciparum Cases (% PF), Annual Parasite Incidence (API), Annual Falciparum Incidence (AFI), Annual Blood Slide Examination Rate (ABER), Slide Positivity Rate (SPR), and Slide Falciparum Rate (SFR). More information about these parameters is discussed in Sam et al., 2025 (Under Review). Further, the Annual Vivax Incidence (AVI) was estimated by subtracting the AFI from API.\u0026nbsp;\u003c/p\u003e\n\u003ch2\u003e2.2\u0026nbsp;Spatial Analysis\u003c/h2\u003e\n\u003cp\u003eFor the spatial plots, we used the official shapefiles available on the Online Maps Portal, maintained by the Ministry of Science \u0026amp; Technology \u003cspan lang=\"EN-IN\"\u003e(Ministry of Space \u0026amp; Technology, 2025)\u003c/span\u003e. We accessed the official government websites for those districts that were mismatched and standardised the district names to ensure consistency with the available malaria data. This step was essential for accurately mapping and plotting the data. Through this, we retrieved 667 districts in 2019, 674 in 2020, 682 in both 2021 and 2022, and 678 in 2023. We then plotted the spatial distribution for each malaria parameter using Geopandas v.0.14.3 (Bossche et al., 2025). The spatial clusters were identified using the Getis-Ord Gi* statistic, which is suitable for comparing the global mean of all districts with the local mean of each district and the corresponding neighbouring districts. Districts having standardised z-scores \u0026gt; 0 and p-values \u0026lt; 0.05 were classified as the hotspots where spatial clustering exists. The Getis-Ord Gi* statistic and their methods have been discussed in detail here \u003cspan lang=\"EN-IN\"\u003e(Getis \u0026amp; Ord, 1992; Sam et al., 2025)\u003c/span\u003e.\u0026nbsp;\u003c/p\u003e\n\u003ch2\u003e2.3\u0026nbsp;Meteorological, socio-economic and Land-use Land-cover covariates\u003c/h2\u003e\n\u003cp\u003eThe meteorological data was collated from the Modern-Era Retrospective Analysis for Research and Applications version 2, or MERRA-2, which provides monthly advanced reanalysis data at a spatial resolution of 0.5\u0026deg;\u0026times;0.625\u0026deg; (Gelaro et al., 2017). We collated the monthly gridded data on surface temperature, precipitation, specific humidity and soil moisture that was overlaid on the district boundaries, for obtaining the district-wise data. This was then aggregated at the annual level to obtain the mean, maximum and minimum for each variable. Data on the land-use land-cover classes were collated from the ESA Sentinel-2 imagery that provided the data at a 10m resolution (Karra et al., 2021). Using the same procedure of overlaying the data, we obtained the areas for water bodies, tree cover, bare lands, built-up areas, snow land, croplands and flooded vegetation for all districts and each year. For the socio-economic data, we used the Household Recode File from the representative National Family Health Survey-5 conducted between 2019-2021 to obtain district-wise household-related information describing the socio-economic characteristics, healthcare choices, nutritional and educational status, and prevalence of common disorders.\u003c/p\u003e\n\u003ch2\u003e2.4\u0026nbsp;Ensemble models\u003c/h2\u003e\n\u003cp\u003eWe first identified three distinct regions that have witnessed the highest degree of transmission observed between 2019 and 2023. The clusters that were identified using the Getis-Ord G* statistics, as discussed in 2.2, also belonged to these three regions. The \u0026apos;Central\u0026apos; regions comprised Telangana, Maharashtra, Chhattisgarh, Odisha and Andhra Pradesh, while the \u0026apos;North\u0026apos; region consisted of Uttar Pradesh and Uttarakhand. The seven states in north-eastern India, namely Assam, Arunachal Pradesh, Meghalaya, Nagaland, Tripura, Mizoram and Manipur, comprised the \u0026apos;North-eastern\u0026apos; region. \u0026nbsp;\u003c/p\u003e\n\u003cp\u003eWe then used an ensemble modelling approach where ensembles of Random Forest Regression Models were developed for each year and region to obtain the feature importance for ranking the variables according to their importance. For obtaining the ranked matrices of the most significant variables, a Monte Carlo Simulation was performed, following which we developed three spatiotemporal Zero-inflated Poisson (ZIP) Regression models for the central, northeast and northern regions of the country separately, as a significant number of districts reported zero API. More information about the methodology can be found in Sam et al., 2025. In contrast to our previous methodology, we here computed the API per 100,000 people to convert all decimals to integers as required for the ZIP, while no categorical variable for mapping the \u003cem\u003eP. falciparum\u003c/em\u003e distribution was introduced. In contrast, we introduced a categorical variable corresponding to the year, accounting for the temporal variations. The spatiotemporal model can be written as:\u0026nbsp;\u003c/p\u003e\n\u003cp\u003e\u003cimg width=\"126\" height=\"23\" src=\"data:image/png;base64,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\" alt=\"image\"\u003e\u003c/p\u003e\n\u003cp\u003ewhere \u003cem\u003ei\u003c/em\u003e denotes the states and \u003cem\u003et\u003c/em\u003e represents the year. For the present study, the Risk Ratios (RR) and the Odds Ratios (OR) were computed by exponentiating the model coefficients for the Poisson and logistic components in the ZIP model, respectively.\u0026nbsp;\u003c/p\u003e\n\u003ch2\u003e2.5\u0026nbsp;Creation of the \u0026apos;MIDAS\u0026apos; Dashboard\u003c/h2\u003e\n\u003cp\u003eWe created an interactive dashboard showing the spatiotemporal variations in the malaria parameters. We used a GeoJSON file to load the geospatial data onto the dashboard. The dashboard was developed using the Dash and Plotly (Plotly Technologies Inc, 2015)\u0026nbsp;frameworks available in Python. Previously, the NIMR-MDB dashboard was developed using R but is currently not hosted for viewing by the general public \u003cspan lang=\"EN-IN\"\u003e(C. P. Yadav \u0026amp; Sharma, 2022)\u003c/span\u003e. We also used data analytical software like Pandas (Reback et al., 2020) and GeoPandas (Jordahl et al., 2019). Our dashboard was structured into three sections to enhance user experience and effective data exploration. The interactive control panel on the left includes dropdown menus and radio buttons that can be used to filter the data by year, geographical regions (states and districts), and malaria indicators that are of interest. The visualisation area on the right shows the spatial and temporal visualisations, where trends and distributions of malaria incidences are depicted. The third section is the header and footer, which sets a context for the general user. For the visualisation components, we have used choropleth maps and time-series maps that track the indicators over time using interactive illustrations. We name our dashboard \u0026quot;MIDAS\u0026quot;, or the Malaria Indicators Dashboard for Analysis and Surveillance. The dashboard has been successfully tested on an internal server and will be made publicly accessible after requisite approvals.\u0026nbsp;\u003c/p\u003e"},{"header":"3.\tResults and Discussion","content":"\u003ch2\u003e3.1\u0026nbsp;Spatiotemporal variations in the malaria parameters across India\u003c/h2\u003e\n\u003cp\u003eIndia reported a cumulative of 0.33 million cases in 2019, which dropped to 0.18 million in 2020 - the year of the COVID-19 pandemic. There was a 13.3% reduction in the cases in 2021, but it increased by 9% in 2022 and again by 29% in 2023 when compared to the previous year. The temporal trends for the Blood Slides Collected (BSC) and Examined (BSE), Rapid Diagnostic Kits (RDT) Collected and Examined, and the Total Number of P. falciparum (Pf\u003csub\u003et\u003c/sub\u003e) and \u003cem\u003eP. vivax\u003c/em\u003e (Pv\u003csub\u003et\u003c/sub\u003e) cases are provided in Table S1. There was a similar drop in the total blood slides collected and examined from 2019 to 2020, which later started improving from 2021 onwards. However, the SPR marginally increased from 0.252 in 2019 to 0.254 in 2020, which later dropped to 0.18 in 2021 and 0.17 in 2023. Both SFR and % PF were higher than the corresponding Slide Vivax Rate and % \u003cem\u003eP. vivax\u003c/em\u003e from 2020 onwards (Sam et al., 2024).\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eAmong the states, Maharashtra had the highest blood slides examined in 2019; however, the neighbouring state of Gujarat reported the highest ABER (24.5), with districts like the Dangs (44.57) and Kachchh (40.29) reporting higher surveillance. In 2019, a \u003cem\u003eP. vivax\u003c/em\u003e outbreak in the densely populated districts of Bareilly (34576) and Budaun (18302) in Uttar Pradesh reported the highest proportion (35.4%) of \u003cem\u003eP. vivax\u003c/em\u003e in the whole country. Subsequently, both of these districts had SPR\u0026gt; 10. Further, the \u003cem\u003eP. falciparum\u0026nbsp;\u003c/em\u003e(% PF \u0026gt; 85) predominant districts of Sukma, Bijapur, Dakshin Bastar Dantewada and Narayanpur in Chhattisgarh, and Lawngtlai, Mamit and Lunglei in Mizoram reported SPR\u0026gt; 5 and API \u0026gt; 15. Interestingly, Nuh in Haryana, which was majorly affected by \u003cem\u003eP. falciparum\u003c/em\u003e (84.7%), reported a high SPR of 5.77 but an API of 0.68 and an ABER of 1.18. \u0026nbsp; \u0026nbsp;\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eIn 2020, the same districts in Chhattisgarh and the north-eastern states, along with Malkangiri in Odisha, reported both API and AFI \u0026gt; 10. Gadchiroli in Maharashtra, which borders Bastar to the east, reported a higher API of 7.7 when compared to 2019 (2.09). It was among the districts having the highest surveillance with an ABER of 75.37. In the subsequent years, Gadchiroli reported an API of 10.47 in 2021, 7.79 in 2022 and 5 in 2023, while the SPR was also restricted to below 1. The eastern city of Kolkata, which is among the world\u0026apos;s most densely populated metropolitan cities, has reported API \u0026gt; 2 since 2019, with a maximum of 5.9 in 2022. Except in 2021 (AFI = 1.5; % PF = 33.3), Kolkata reported AFI \u0026lt; 1, while the % PF varied between 5.5-14.5, highlighting the significance of \u003cem\u003eP. vivax\u003c/em\u003e in the malaria transmission.\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eWe note that P. falciparum-predominant regions have consistently been the same throughout the years \u0026ndash; it is primarily dominant in Central India and North-eastern India. Consequently, these are the regions that have reported very high API and AFI \u0026gt; 10. For instance, Lawngtlai in Mizoram has reported very high P. falciparum-based transmission for all five years, which was the maximum for the whole country in 2021 (API = 26.2; AFI = 22.4; SPR: 4.1), 2022 (API = 39.3; AFI = 30.3, SPR: 4.8) and in 2023 (API = 56.2; AFI = 38.9; SPR: 16.6). However, a transition to \u003cem\u003eP. vivax\u003c/em\u003e was observed in Northeast India. A very high \u003cem\u003eP. vivax\u003c/em\u003e transmission was observed in Lawngtlai, Mamit and Lunglei in Mizoram and Dhalai and South Tripura in Tripura. In Lawngtlai, there was a 213% increase in the AVI in 2020 when compared to 2019. The transmission further intensified in 2022 and 2023, as an AVI of 9.0 and 17.6 was reported in Lawngtai. A similar pattern was observed for the remaining districts (Figure 3), which also share international borders with Myanmar and Bangladesh. Previously, cross-boundary malaria was highlighted as a potential risk factor for malaria resurgence in the region (Kumari et al., 2022; Sam et al., 2024). The spatial distribution of API across the districts is provided in Figure 1, while the distribution of AVI is provided in the supplementary.\u003c/p\u003e\n\u003ch2\u003e3.2\u0026nbsp;Identification of spatial clusters using Getis-Ord Gi* Statistics\u003c/h2\u003e\n\u003cp\u003eWe classified the districts further based on their Getis-Ord Z-scores and the associated p-values. Districts with z-scores greater than 0 and p-values \u0026lt; 0.05 were classified as hotspots \u003cspan lang=\"EN-IN\"\u003e(Getis \u0026amp; Ord, 1992).\u003c/span\u003e We observe that the hotspots are distributed in the same districts only from 2019 to 2024. For API, these districts are distributed across two distinct regions in the country, namely the Central Region covering Maharashtra (1), Andhra Pradesh (4), Telangana (1), Chhattisgarh (6), and Odisha (2), and the Northeast Region spanning across Assam (2), Mizoram (8), and Tripura (8). An additional zone in the northern parts of the country that covers Uttar Pradesh and Uttarakhand was observed. The significant hotspots observed for (a) API, (b) AFI, and (c) AVI are provided in Figure 2, while the spatial maps and the intensity of the transmission are provided in Figure 3.\u003c/p\u003e\n\u003cp\u003eFor API, we observe that Bastar (Z-score: 4.95), Dastin Bastar Dantewada (Z-score: 4.71) and Sukma (Z-score: 4.5) in the Central Zone show highly significant clustering in 2019. The neighbouring districts of Narayanpur (Z-score: 3.0), Kondagaon (Z-score: 2.97) and Gadchiroli (Z-score: 2.47) are also identified as hotspots. We observe that these districts show a lesser extent of clustering over the years as their Z-scores reduce below 2 in 2023 (Figure 2). In contrast, the districts in northeast India, such as Saiha, Lawngtlai, Serchhip, Lunglei, Champai \u0026amp; Mamit, show increasing Z-scores, with the maximum in 2023. For instance, Saiha and Lunglei reported Z-scores of 4.87 and 4.78, respectively. The eight districts in Tripura also reported maximum Z-scores in 2023. Hailakandi in Assam and Kolasib in Mizoram emerged as hotspots in 2023. Further, the districts in Andhra Pradesh and Telangana were identified as hotspots in 2019 and 2020 only.\u003c/p\u003e\n\u003cp\u003eSimilar to the API, the significant hotspots for the AFI were restricted broadly to the central and northeast parts of the country. The districts in the central region exhibited very high clustering between 2019 and 2021, which declined slightly in 2022 and 2023. For instance, Bastar in Chhattisgarh reported a Z-score of 4.77 in 2019, which decreased to 3.76 in 2021 and 2.58 in 2023. The neighbouring districts of Sukma and Dakshin Bastar Dantewada in Chhattisgarh that reported very high Z-scores \u0026gt; 4 also followed a similar trend. In contrast, the clustering in north-eastern districts, especially those in Mizoram (Saiha, Serchhip, Lawngtlai and Champai), reported increased clustering in the later years as the Z-scores were \u0026gt; 4. The clustering in Tripura reported relatively moderate clustering with Z-scores ~ 2.1, which reduced in the later years. A few districts that reported very low transmission, such as Hailakandi in Assam, were also categorised as high-risk areas due to the neighbouring districts reporting very high API (Figure S5).\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eWe observe a geographical shift in the clusters observed for AVI that is also evident in the spatial distribution maps of AVI throughout the years (Figure S1; Section 3.1). All five districts that emerged as the focal point of AVI transmission, namely Lawngtlai, Mamit and Lunglei in Mizoram and Dhalai and South Tripura in Tripura, were all classified as hotspots for AVI. Thus, the emergence of \u003cem\u003eP. vivax\u003c/em\u003e is occurring in this part of the country that was previously dominated by \u003cem\u003eP. falciparum\u003c/em\u003e. In the north, the districts around Bareilly were identified as significant hotspots in 2019 and 2020, but the clustering was not significant in the subsequent years as these regions also witnessed fewer cases (Figure 1). Likewise, a similar trend was observed in the central region as districts like Sukma and Uttar Bastar Kanker, which are also categorised as significant hotspots for AFI, did not emerge as clusters for AVI post-2021. However, in contrast, the districts in north-eastern India showed very strong clustering after 2021. Districts in Mizoram, such as Saiha, Lawngtai, Lunglei and Serchhip, showed Z-scores \u0026gt; 5 in 2023 and \u0026gt; 4.5 in both 2022 and 2021, while all eight districts in Tripura were classified as significant hotspots with the highest degree of clustering in 2023.\u003c/p\u003e\n\u003ch2\u003e3.3\u0026nbsp;Identifying potential risk factors for malaria transmission using the spatiotemporal ensemble model\u003c/h2\u003e\n\u003cp\u003eUsing the region-specific ensemble of Random Forest Regression and Zero-inflated Poisson Regression models, the significant covariates that are likely influencing malaria transmission were identified for each of the parameters, i.e. API, AFI and AVI. The estimated region-wise associations or the Risk Ratios for API, AFI and AVI in districts reporting \u0026ge; 0 are provided in Figure 4. We observe that for API in the Central Region, % total of Scheduled Castes and Scheduled Tribes (RR: 2.18 (95% CI: 2.1, 2.27)), % population not having mobile (RR: 1.7 (95% CI: 1.68, 1.73)) and % population who are not having normal BMI (RR: 1.06 (95% CI: 1.03, 1.08)) are among the socio-economic determinants positively associated with increased malaria transmission in districts. In our previous work, we found the same factors responsible for the malaria risk for the entire country (Sam et al., 2025; Under Review). Obesity has been previously identified as a risk factor in Sweden (Wyss et al., 2017), while malnutrition was associated with malaria in Cameroon (Kojom Foko et al., 2021).\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eWe also observe that % of households (HH) owning livestock is negatively associated with malaria in all regions for API (0.3 \u0026lt; RR \u0026lt; 0.7), but it is positively associated with AVI in the Central (RR: 1.3 (95% CI: 1.19, 1.42)). Livestock-based interventions have been recommended as a strategy for controlling malaria\u0026nbsp;\u003cspan lang=\"EN-IN\"\u003e(Franco et al., 2014)\u003c/span\u003e, but the in-house raising of animals in Indonesia \u003cspan lang=\"EN-IN\"\u003e(Hasyim et al., 2018)\u003c/span\u003e and the presence of cattle in households in Tanzania were associated with malaria \u003cspan lang=\"EN-IN\"\u003e(Mayagaya et al., 2015)\u003c/span\u003e. Thus, more evidence-based research is needed to ascertain the role of livestock in malaria control. Similarly, a mother\u0026apos;s education is negatively associated with API in all three regions, but we observe a positive association with AVI in the Central Region (RR: 1.7 (95% CI: 1.53, 1.88)). An educated mother will be aware of the symptoms of malaria. During outbreaks, testing and diagnosis increase due to pre-existing knowledge about the symptoms. This could lead to more cases being reported to the system. Similarly, in the absence of outbreaks, awareness about the prevention measures and careful adoption of the interventions will reduce the risk of malaria \u003cspan lang=\"EN-IN\"\u003e(Njau et al., 2014)\u003c/span\u003e. \u0026nbsp; \u0026nbsp;\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eHealthcare accessibility, which is indicated by factors such as % of the population accessing treatment from private doctors or public hospitals, is negatively associated with the malaria risk for all regions and parameters. We also observe that % of HH having Rashtriya Swasthya Bima Yojana (RSBY) is positively associated with malaria parameters in multiple regions. The RSBY is a flagship programme of the Ministry of Health, Government of India that offers health insurance coverage to families below the poverty line. Economically marginalised households are more likely to access healthcare facilities due to their health insurance coverage (Thomas, 2016).\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eIn the north-eastern region, factors such as % HH living in muddy walled structures as well as % HH belonging to the poorest wealth index are positively associated with API, AFI and AVI. Economically disadvantaged communities are among the most vulnerable sections in this region, as earlier reported in Assam (K. Yadav et al., 2014). The percentage of HH using unprotected drinking water from sources like natural springs is also associated with the API (RR: 1.29 (95% CI: 1.28, 1.3)) and AFI (RR: 1.24 (95% CI: 1.23, 1.25)), as also reported in Ethiopia (Yang et al., 2020). Previously, these muddy houses have been linked to an increased risk of malaria in Mandla, India (Sharma et al., 2021). We also observe a significant positive association shown by % HH using Insecticide Treated Nets (ITNs) in the northeast with API (RR: 3.5 (95% CI: 3.36, 3.64)), AFI (RR: 2.27 (95% CI: 2.16, 2.39)) and AVI (RR: 3.45 (95% CI: 3.2, 3.71)). In contrast, the % HH using ITNs had a negative association with the API (RR: 0.15 (95% CI: 0.14, 0.17)) and AVI (RR: 0.26 (95% CI: 0.23, 0.29)) in the North Region. This implies that outdoor transmission could be responsible for the malaria outbreaks in the north-eastern region. Contrarily, only a few districts, such as Budaun, reported high transmission in the North, and they had a very low proportion (1.7%) of HHs using ITNs. Thus, with less ITN usage, it is likely that the cases increased during outbreaks.\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eAdditionally, in the north, we also observe that both % of the population using rainwater for drinking purposes and % of the population fetching water elsewhere for household usage (RR: 4.54 (95% CI: 4.19, 4.9)) are very strongly associated with the API. In Kolkata and Chennai, \u003cem\u003eAnopheles Stephensi\u003c/em\u003e has reportedly been found in overhead water tanks, which had been kept open by residents to collect rainfall for later usage (Mandal et al., 2011). Thus, water storage practices in this northern belt could be responsible for the increased outbreaks. The 2018 outbreak in Bareilly, a district in Uttar Pradesh, was also attributed to excessive rainfall, along with poor surveillance (Kamal et al., 2020). Moreover, travelling to fetch water has been linked to increased cases in Africa (Ahmed et al., 2020; Minale \u0026amp; Alemu, 2018). In the northeast, we observe that % of HH having a water source in their own yard is also positively associated with the AVI (RR: 1.55 (95% CI: 1.42, 1.7)). In Tanzania, increasing coverage of non-piped water was associated with rising malaria cases (Shayo et al., 2021). Additionally, the prevalence of tobacco non-smokers was positively associated with malaria in the north. In Nigeria, decreased endophily for Anopheles was previously reported in a room that was habitated by smokers; however, the role of tobacco smoking habits needs to be investigated (Obembe et al., 2018).\u003c/p\u003e\n\u003cp\u003eThe forested land area defined by the \u0026apos;Trees\u0026apos; variable was positively associated with API, AFI and AVI in both the Central and Northeast regions. This was complemented by the meteorological variables like the maximum of both precipitation and specific humidity. In the north, agricultural land defined by the LULC variable \u0026apos;crops\u0026apos; was positively associated with both API and AVI. To investigate the temporal factor, the categorical variables\u0026apos; Year\u0026apos; for 2020, 2021, 2022 and 2023 were included with 2019 as the reference. We obtained a significant negative association for these variables with API, AFI and AVI for both the central and northern regions, reflecting a decrease in cases. However, a significant positive association was shown with API in 2023 and with AVI in 2020, 2021 and 2022 for the northeast region. Thus, our model could capture the increase in AVI in the north-eastern region, as also observed in Figure 2. The estimated ORs for the districts reporting API, AFI and AVI = 0 are provided in the supplementary. Overall, the models reported MSEs \u0026lt; 0.3 for AVI, between 0.15 and 2.6 for API and \u0026lt; 1.9 for AFI, thus indicating the suitability of the models.\u0026nbsp;\u003c/p\u003e\n\u003ch2\u003e3.4 Dashboard\u003c/h2\u003e\n\u003cp\u003eOur \u0026apos;MIDAS\u0026apos; dashboard provides the spatiotemporal mapping of malaria indicators for all districts between 2019 and 2023. On the left panel, the user can choose between spatial and temporal variations. For both, there are dropdown menus through which a user can select the year and the parameters of interest. After initialisation, the spatial maps and temporal plots are generated. Using the mouse, the data for all districts can be viewed. The temporal maps provide the annual change in the malaria parameters for each district. The snapshot for the dashboard is provided in Figure 5, while the detailed Standard Operating Procedure is provided as supplementary material.\u0026nbsp;\u003c/p\u003e"},{"header":"4. Conclusion","content":"\u003cp\u003eThrough this work, we map the spatiotemporal distributions of malaria indicators between 2019 and 2023. We observe that malaria has reduced in the last five years, compared to the previous decades, although there is a marginal increase in 2023 when compared to 2022. The significant hotspots for API, AVI and AFI are concentrated in Central India and North-eastern India; however, the clusters for AVI were also found in the northern states of Uttar Pradesh and Uttarakhand. A geographical expansion in the clusters for AVI is observed in Northeast India throughout the years. This unprecedented increase in \u003cem\u003eP. vivax\u003c/em\u003e has been confirmed microscopically and molecularly at subcentre and village spatial levels (Unpublished Data). Our region-specific spatiotemporal models for each indicator suggest that while economically marginalised communities continue to be the most vulnerable sections, drinking water practices, maternal education, and healthcare accessibility are the likely drivers of the transmission. We believe that simple behavioural changes in the population, such as periodic overhead water tank cleaning or adopting ITNs and a healthy lifestyle, could reduce the malaria burden. Our dashboard is expected to raise awareness among the general public and help the stakeholders involved in malaria control in tracking the malaria indicators over the years. Our study uses annual data, where the true impact of seasonality can not be measured. Further, while the ecological study design is helpful in assessing the population-level patterns, the risks reported here should be reassessed through cross-sectional or longitudinal study designs to avoid potential bias, although similar associations have been reported elsewhere. We also recommend to the stakeholders to include the identified variables during data collection on reported malaria cases. Future work should also focus on longer temporal data to assess the impact of weather variables. We hope that our study will help the stakeholders and generate awareness among the general public of the country. Let\u0026apos;s end malaria once and for all together!\u0026nbsp;\u003c/p\u003e"},{"header":"Declarations","content":"\u003ch2\u003eFunding:\u003c/h2\u003e \u003cp\u003eFunding for this study was provided by the Gates Foundation (NV-044445). AS wants to thank the Ministry of Education for providing the Prime Minister Research Fellowship (ID-1302077).\u003c/p\u003e\u003ch2\u003eAcknowledgements:\u003c/h2\u003e \u003cp\u003eThe authors thank the National Centre for Vector Borne Disease Control Programme for the malaria data, the Indian Institute for Population Science and the Demographic and Health Survey for the National Family Health Survey data, and the National Aeronautics and Space Administration for the meteorological data. The authors thank Dr. Tanu Jain (Director, NCVBDC), Dr. Pranab Jyoti Bhuyan (Additional Director, NCVBDC) and the malaria team at the NCVBDC for their valuable insights. The work is based on research findings by the authors and not the opinion of the government.\u003c/p\u003e"},{"header":"References","content":"\u003col\u003e\n\u003cli\u003eAhmed, S., Reithinger, R., Kaptoge, S. K., \u0026amp; Ngondi, J. M. (2020). Travel Is a Key Risk Factor for Malaria Transmission in Pre-Elimination Settings in Sub-Saharan Africa: A Review of the Literature and Meta-Analysis. \u003cem\u003eThe American Journal of Tropical Medicine and Hygiene\u003c/em\u003e, \u003cem\u003e103\u003c/em\u003e(4), 1380. https://doi.org/10.4269/AJTMH.18-0456\u003c/li\u003e\n\u003cli\u003eBossche, J. Van den, Jordahl, K., Fleischmann, M., Richards, M., McBride, J., Wasserman, J., Badaracco, A. G., Snow, A. D., Ward, B., Tratner, J., Gerard, J., Perry, M., cjqf, Hjelle, G. A., Taves, M., Hoeven, E. ter, Cochran, M., Bell, R., rraymondgh, \u0026hellip; Gardiner, J. (n.d.). \u003cem\u003egeopandas/geopandas: v1.0.1\u003c/em\u003e. https://doi.org/10.5281/ZENODO.12625316\u003c/li\u003e\n\u003cli\u003eFranco, A. O., Gomes, M. G. M., Rowland, M., Coleman, P. G., \u0026amp; Davies, C. R. (2014). Controlling Malaria Using Livestock-Based Interventions: A One Health Approach. \u003cem\u003ePLOS ONE\u003c/em\u003e, \u003cem\u003e9\u003c/em\u003e(7), e101699. https://doi.org/10.1371/JOURNAL.PONE.0101699\u003c/li\u003e\n\u003cli\u003eGelaro, R., McCarty, W., Su\u0026aacute;rez, M. J., Todling, R., Molod, A., Takacs, L., Randles, C. A., Darmenov, A., Bosilovich, M. G., Reichle, R., Wargan, K., Coy, L., Cullather, R., Draper, C., Akella, S., Buchard, V., Conaty, A., da Silva, A. M., Gu, W., \u0026hellip; Zhao, B. (2017). The Modern-Era Retrospective Analysis for Research and Applications, Version 2 (MERRA-2). \u003cem\u003eJournal of Climate\u003c/em\u003e, \u003cem\u003e30\u003c/em\u003e(14), 5419\u0026ndash;5454. https://doi.org/10.1175/JCLI-D-16-0758.1\u003c/li\u003e\n\u003cli\u003eGetis, A., \u0026amp; Ord, J. K. (1992). The Analysis of Spatial Association by Use of Distance Statistics. \u003cem\u003eGeographical Analysis\u003c/em\u003e, \u003cem\u003e24\u003c/em\u003e(3), 189\u0026ndash;206. https://doi.org/10.1111/J.1538-4632.1992.TB00261.X\u003c/li\u003e\n\u003cli\u003eHasyim, H., Dhimal, M., Bauer, J., Montag, D., Groneberg, D. A., Kuch, U., \u0026amp; M\u0026uuml;ller, R. (2018). Does livestock protect from malaria or facilitate malaria prevalence? A cross-sectional study in endemic rural areas of Indonesia. \u003cem\u003eMalaria Journal\u003c/em\u003e, \u003cem\u003e17\u003c/em\u003e(1), 1\u0026ndash;11. https://doi.org/10.1186/S12936-018-2447-6/TABLES/2\u003c/li\u003e\n\u003cli\u003eJordahl, K., Van Den Bossche, J., Wasserman, J., McBride, J., Gerard, J., Tratner, J., Perry, M., \u0026amp; Farmer, C. (n.d.). geopandas/geopandas: v0.5.0. \u003cem\u003eZndo\u003c/em\u003e. https://doi.org/10.5281/ZENODO.2705946\u003c/li\u003e\n\u003cli\u003eKamal, S., Chandra, R., Mittra, K. K., \u0026amp; Sharma, S. N. (2020). An investigation into outbreak of malaria in Bareilly district of Uttar Pradesh, India. \u003cem\u003eJournal of Communicable Diseases\u003c/em\u003e, \u003cem\u003e52\u003c/em\u003e(4), 1\u0026ndash;11. https://doi.org/10.24321/0019.5138.202034\u003c/li\u003e\n\u003cli\u003eKarra, K., Kontgis, C., Statman-Weil, Z., Mazzariello, J. C., Mathis, M., \u0026amp; Brumby, S. P. (2021). GLOBAL LAND USE/LAND COVER WITH SENTINEL 2 AND DEEP LEARNING. \u003cem\u003eInternational Geoscience and Remote Sensing Symposium (IGARSS)\u003c/em\u003e, \u003cem\u003e2021-July\u003c/em\u003e, 4704\u0026ndash;4707. https://doi.org/10.1109/IGARSS47720.2021.9553499\u003c/li\u003e\n\u003cli\u003eKojom Foko, L. P., Nolla, N. P., Nyabeyeu Nyabeyeu, H., Tonga, C., \u0026amp; Lehman, L. G. (2021). Prevalence, Patterns, and Determinants of Malaria and Malnutrition in Douala, Cameroon: A Cross-Sectional Community-Based Study. \u003cem\u003eBioMed Research International\u003c/em\u003e, \u003cem\u003e2021\u003c/em\u003e(1), 5553344. https://doi.org/10.1155/2021/5553344\u003c/li\u003e\n\u003cli\u003eKraemer, M. U. G., Hay, S. I., Pigott, D. M., Smith, D. L., Wint, G. R. W., \u0026amp; Golding, N. (2016). Progress and Challenges in Infectious Disease Cartography. \u003cem\u003eTrends in Parasitology\u003c/em\u003e, \u003cem\u003e32\u003c/em\u003e(1), 19\u0026ndash;29. https://doi.org/10.1016/J.PT.2015.09.006\u003c/li\u003e\n\u003cli\u003eKumar, G., Gupta, S., Kaur, J., Pasi, S., Baharia, R., Mohanty, A. K., Goel, P., Sharma, A., \u0026amp; Rahi, M. (2024). Mapping malaria vectors and insecticide resistance in a high-endemic district of Haryana, India: implications for vector control strategies. \u003cem\u003eMalaria Journal\u003c/em\u003e, \u003cem\u003e23\u003c/em\u003e(1), 1\u0026ndash;11. https://doi.org/10.1186/S12936-023-04797-8/TABLES/5\u003c/li\u003e\n\u003cli\u003eKumari, R., Kumar, A., Dhingra, N., \u0026amp; Sharma, S. N. (2022). Transition of Malaria Control to Malaria Elimination in India. In \u003cem\u003eJournal of Communicable Diseases\u003c/em\u003e (Vol. 54, Issue 1, pp. 124\u0026ndash;140). Indian Society for Malaria and Communicable Diseases. https://doi.org/10.24321/0019.5138.202259\u003c/li\u003e\n\u003cli\u003eMandal, B., Biswas, B., Banerjee, A., Mukherjee, T. K., Nandi, J., \u0026amp; Biswas, \u0026amp; D. (2011). Breeding propensity of Anopheles stephensi in chlorinated and rainwater containers in Kolkata City, India. \u003cem\u003eJ Vector Borne Dis\u003c/em\u003e, \u003cem\u003e48\u003c/em\u003e, 58\u0026ndash;60. www.mrcindia.org/chennai.hmt.\u003c/li\u003e\n\u003cli\u003eMayagaya, V. S., Nkwengulila, G., Lyimo, I. N., Kihonda, J., Mtambala, H., Ngonyani, H., Russell, T. L., \u0026amp; Ferguson, H. M. (2015). The impact of livestock on the abundance, resting behaviour and sporozoite rate of malaria vectors in southern Tanzania. \u003cem\u003eMalaria Journal\u003c/em\u003e, \u003cem\u003e14\u003c/em\u003e(1), 1\u0026ndash;14. https://doi.org/10.1186/S12936-014-0536-8/TABLES/4\u003c/li\u003e\n\u003cli\u003eMinale, A. S., \u0026amp; Alemu, K. (2018). Mapping malaria risk using geographic information systems and remote sensing: The case of Bahir Dar City, Ethiopia. \u003cem\u003eGeospatial Health\u003c/em\u003e, \u003cem\u003e13\u003c/em\u003e(1), 157\u0026ndash;163. https://doi.org/10.4081/gh.2018.660\u003c/li\u003e\n\u003cli\u003eMinistry of Space \u0026amp; Technology. (2025). \u003cem\u003eSurvey of India\u003c/em\u003e. https://onlinemaps.surveyofindia.gov.in/Digital_Product_Show.aspx\u003c/li\u003e\n\u003cli\u003eNjau, J. D., Stephenson, R., Menon, M. P., Kachur, S. P., \u0026amp; McFarland, D. A. (2014). Investigating the Important Correlates of Maternal Education and Childhood Malaria Infections. \u003cem\u003eThe American Journal of Tropical Medicine and Hygiene\u003c/em\u003e, \u003cem\u003e91\u003c/em\u003e(3), 509\u0026ndash;519. https://doi.org/10.4269/AJTMH.13-0713\u003c/li\u003e\n\u003cli\u003eObembe, A., Popoola, K. O. K., Oduola, A. O., \u0026amp; Awolola, S. T. (2018). Differential behaviour of endophilic Anopheles mosquitoes in rooms occupied by tobacco smokers and non-smokers in two Nigerian villages. \u003cem\u003eJournal of Applied Sciences and Environmental Management\u003c/em\u003e, \u003cem\u003e22\u003c/em\u003e(6), 981\u0026ndash;985. https://doi.org/10.4314/JASEM.V22I6.23\u003c/li\u003e\n\u003cli\u003eOdhiambo, J. N., Kalinda, C., MacHaria, P. M., Snow, R. W., \u0026amp; Sartorius, B. (2020). Spatial and spatio-temporal methods for mapping malaria risk: a systematic review. \u003cem\u003eBMJ Global Health\u003c/em\u003e, \u003cem\u003e5\u003c/em\u003e(10), 2919. https://doi.org/10.1136/BMJGH-2020-002919\u003c/li\u003e\n\u003cli\u003ePlotly Technologies Inc. (2015). \u003cem\u003eCollaborative data science\u003c/em\u003e. Plotly Technologies Inc.\u003c/li\u003e\n\u003cli\u003eRahi, M., \u0026amp; Sharma, A. (2022). Malaria control initiatives that have the potential to be gamechangers in India\u0026apos;s quest for malaria elimination. \u003cem\u003eThe Lancet Regional Health - Southeast Asia\u003c/em\u003e, \u003cem\u003e2\u003c/em\u003e, 100009. https://doi.org/10.1016/j.lansea.2022.04.005\u003c/li\u003e\n\u003cli\u003eReback, J., McKinney, W., Jbrockmendel, Van Den Bossche, J., Augspurger, T., Cloud, P., Gfyoung, Sinhrks, Klein, A., Hawkins, S., Roeschke, M., Tratner, J., She, C., Ayd, W., Petersen, T., MomIsBestFriend, Garcia, M., Schendel, J., Hayden, A., \u0026hellip; Winkel, M. (2020). pandas-dev/pandas: Pandas 1.0.5. \u003cem\u003eZndo\u003c/em\u003e. https://doi.org/10.5281/ZENODO.3898987\u003c/li\u003e\n\u003cli\u003eSam, A. K., Karmakar, S., Mukhopadhyay, S., \u0026amp; Phuleria, H. C. (2024). A historical perspective of malaria policy and control in India. \u003cem\u003eIJID Regions\u003c/em\u003e, \u003cem\u003e12\u003c/em\u003e, 100428. https://doi.org/10.1016/J.IJREGI.2024.100428\u003c/li\u003e\n\u003cli\u003eSarkar, A., Kumar, V., Jasrotia, A. S., Taloor, A. K., Kumar, R., Sharma, R., Khajuria, V., Raina, G., Kouser, B., \u0026amp; Roy, S. (2020). \u003cem\u003eSpatial Analysis and Mapping of Malaria Risk in Dehradun City India: A Geospatial Technology-Based Decision-Making Tool for Planning and Management\u003c/em\u003e. 207\u0026ndash;221. https://doi.org/10.1007/978-981-15-2097-6_14\u003c/li\u003e\n\u003cli\u003eSarkar, S., Singh, P., Lingala, M. A. L., Verma, P., \u0026amp; Dhiman, R. C. (2019). Malaria risk map for India based on climate, ecology and geographical modelling. \u003cem\u003eGeospatial Health\u003c/em\u003e, \u003cem\u003e14\u003c/em\u003e(2), 281\u0026ndash;292. https://doi.org/10.4081/gh.2019.767\u003c/li\u003e\n\u003cli\u003eSharma, R. K., Rajvanshi, H., Bharti, P. K., Nisar, S., Jayswar, H., Mishra, A. K., Saha, K. B., Shukla, M. M., Das, A., Kaur, H., Wattal, S. L., \u0026amp; Lal, A. A. (2021). Socio-economic determinants of malaria in tribal dominated Mandla district enrolled in Malaria Elimination Demonstration Project in Madhya Pradesh. \u003cem\u003eMalaria Journal\u003c/em\u003e, \u003cem\u003e20\u003c/em\u003e(1), 1\u0026ndash;13. https://doi.org/10.1186/S12936-020-03540-X/TABLES/4\u003c/li\u003e\n\u003cli\u003eShayo, F. K., Nakamura, K., Al-Sobaihi, S., \u0026amp; Seino, K. (2021). Is the source of domestic water associated with the risk of malaria infection? Spatial variability and a mixed-effects multilevel analysis. \u003cem\u003eInternational Journal of Infectious Diseases\u003c/em\u003e, \u003cem\u003e104\u003c/em\u003e, 224\u0026ndash;231. https://doi.org/10.1016/J.IJID.2020.12.062\u003c/li\u003e\n\u003cli\u003eSingh, P., Lingala, M. A. L., Sarkar, S., \u0026amp; Dhiman, R. C. (2017). Mapping of Malaria Vectors at District Level in India: Changing Scenario and Identified Gaps. \u003cem\u003eHttps://Home.Liebertpub.Com/Vbz\u003c/em\u003e, \u003cem\u003e17\u003c/em\u003e(2), 91\u0026ndash;98. https://doi.org/10.1089/VBZ.2016.2018\u003c/li\u003e\n\u003cli\u003eSnow, R. W., Marsh, K., \u0026amp; Le Sueur, D. (1996). The need for maps of transmission intensity to guide malaria control in Africa. \u003cem\u003eParasitology Today\u003c/em\u003e, \u003cem\u003e12\u003c/em\u003e(12), 455\u0026ndash;457. https://doi.org/10.1016/S0169-4758(96)30032-X\u003c/li\u003e\n\u003cli\u003eSnow, R. W., \u0026amp; Noor, A. M. (2015). \u003cem\u003eMalaria risk mapping in Africa The historical context to the Information for Malaria (INFORM) project\u003c/em\u003e.\u003c/li\u003e\n\u003cli\u003eThomas, T. K. (2016). Role of health insurance in enabling universal health coverage in India: A critical review. \u003cem\u003eHealth Services Management Research\u003c/em\u003e, \u003cem\u003e29\u003c/em\u003e(4), 99\u0026ndash;106. https://doi.org/10.1177/0951484816670191/ASSET/D98EA4BB-0994-4C0B-AE48-F95F055111DA/ASSETS/IMAGES/LARGE/10.1177_0951484816670191-FIG3.JPG\u003c/li\u003e\n\u003cli\u003eWimberly, M. C., de Beurs, K. M., Loboda, T. V., \u0026amp; Pan, W. K. (2021). Satellite Observations and Malaria: New Opportunities for Research and Applications. \u003cem\u003eTrends in Parasitology\u003c/em\u003e, \u003cem\u003e37\u003c/em\u003e(6), 525\u0026ndash;537. https://doi.org/10.1016/J.PT.2021.03.003/ATTACHMENT/A6F80937-DD23-43E2-B10A-3606AAC53BB1/MMC1.DOCX\u003c/li\u003e\n\u003cli\u003eWorld Health Organization. (2024). \u003cem\u003eGlobal Malaria Programme operational strategy 2024-2030\u003c/em\u003e. 01\u0026ndash;84.\u003c/li\u003e\n\u003cli\u003e\u003cem\u003eWorld malaria report 2024\u003c/em\u003e. (2024). World Health Organisation. https://www.who.int/teams/global-malaria-programme/reports/world-malaria-report-2024\u003c/li\u003e\n\u003cli\u003eWyss, K., W\u0026aring;ngdahl, A., Vesterlund, M., Hammar, U., Dashti, S., Naucler, P., \u0026amp; F\u0026auml;rnert, A. (2017). Obesity and Diabetes as Risk Factors for Severe Plasmodium falciparum Malaria: Results From a Swedish Nationwide Study. \u003cem\u003eClinical Infectious Diseases\u003c/em\u003e, \u003cem\u003e65\u003c/em\u003e(6), 949\u0026ndash;958. https://doi.org/10.1093/CID/CIX437\u003c/li\u003e\n\u003cli\u003eYadav, C. P., \u0026amp; Sharma, A. (2022). National Institute of Malaria Research-Malaria Dashboard (NIMR-MDB): A digital platform for analysis and visualisation of epidemiological data. \u003cem\u003eThe Lancet Regional Health - Southeast Asia\u003c/em\u003e, \u003cem\u003e5\u003c/em\u003e. https://doi.org/10.1016/j.lansea.2022.100030\u003c/li\u003e\n\u003cli\u003eYadav, K., Dhiman, S., Rabha, B., Saikia, P. K., \u0026amp; Veer, V. (2014). Socio-economic determinants for malaria transmission risk in an endemic primary health centre in Assam, India. \u003cem\u003eInfectious Diseases of Poverty\u003c/em\u003e, \u003cem\u003e3\u003c/em\u003e(1), 1\u0026ndash;8. https://doi.org/10.1186/2049-9957-3-19/TABLES/3\u003c/li\u003e\n\u003cli\u003eYang, D., He, Y., Wu, B., Deng, Y., Li, M., Yang, Q., Huang, L., Cao, Y., \u0026amp; Liu, Y. (2020). Drinking water and sanitation conditions are associated with the risk of malaria among children under five years old in sub-Saharan Africa: A logistic regression model analysis of national survey data. \u003cem\u003eJournal of Advanced Research\u003c/em\u003e, \u003cem\u003e21\u003c/em\u003e, 1\u0026ndash;13. https://doi.org/10.1016/J.JARE.2019.09.001\u003c/li\u003e\n\u003cli\u003eYe, Y., \u0026amp; Andrada, A. (2020). Estimating Malaria Incidence through Modeling Is a Good Academic Exercise, but How Practical Is It in High-Burden Settings? \u003cem\u003eThe American Journal of Tropical Medicine and Hygiene\u003c/em\u003e, \u003cem\u003e102\u003c/em\u003e(4), 701\u0026ndash;702. https://doi.org/10.4269/AJTMH.20-0120\u003c/li\u003e\n\u003c/ol\u003e"}],"fulltextSource":"","fullText":"","funders":[],"hasAdminPriorityOnWorkflow":false,"hasManuscriptDocX":true,"hasOptedInToPreprint":true,"hasPassedJournalQc":"","hasAnyPriority":true,"hideJournal":true,"highlight":"","institution":"","isAcceptedByJournal":false,"isAuthorSuppliedPdf":false,"isDeskRejected":"","isHiddenFromSearch":false,"isInQc":false,"isInWorkflow":false,"isPdf":false,"isPdfUpToDate":true,"isWithdrawnOrRetracted":false,"journal":{"display":true,"email":"[email protected]","identity":"researchsquare","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":true,"externalIdentity":"","sideBox":"","snPcode":"","submissionUrl":"/submission","title":"Research Square","twitterHandle":"researchsquare","acdcEnabled":true,"dfaEnabled":false,"editorialSystem":"","reportingPortfolio":"","inReviewEnabled":false,"inReviewRevisionsEnabled":true},"keywords":"Malaria, Mapping, Digital dashboard, MIDAS, Socio-economic inequities, Policy","lastPublishedDoi":"10.21203/rs.3.rs-6781302/v1","lastPublishedDoiUrl":"https://doi.org/10.21203/rs.3.rs-6781302/v1","license":{"name":"CC BY 4.0","url":"https://creativecommons.org/licenses/by/4.0/"},"manuscriptAbstract":"\u003cp\u003eWith less than two years remaining from 2027 – the year which the government has targeted to achieve zero Indigenous cases, we map the malaria indicators across the 700+ districts for five years between 2019 and 2023 using spatiotemporal maps and also assess the potential drivers of malaria transmission in different regions. We used the annual district-wise malaria data from the National Center for Vector Borne Disease Control Programme (NCVBDC) and the cross-sectional socio-economic data from the National Family Health Survey. We also collated the meteorological and land-use land-cover data from the MERRA-2 and Sentinel-LPA satellites, respectively. We then developed region-specific ensembles of spatiotemporal models that allowed us to identify the associated covariates while the regions were identified using the Getis-Ord Gi* statistics. With 0.33 million malaria cases in 2019, the COVID-19 pandemic led to a significant reduction in reported cases. The \u003cem\u003eP. falciparum\u003c/em\u003e affected regions are widespread in North-eastern and Central India. However, after the pandemic, an emerging geographical expansion into the north-eastern parts is observed for the \u003cem\u003eP. vivax\u003c/em\u003e, which is evident from the clusters and the spatiotemporal ensemble models. Population belonging to scheduled castes and scheduled tribes and those economically marginalised are among the most vulnerable, but lifestyle habits such as drinking water practices, maternal education, and healthcare accessibility are identified as the potential drivers of malaria transmission. We also developed a digital dashboard that allows the general public and the stakeholders to track the malaria indicators for each district and the corresponding year.\u003c/p\u003e","manuscriptTitle":"Mapping Malaria Risk in India between 2019-2023: A Tool for the Public to Track Malaria","msid":"","msnumber":"","nonDraftVersions":[{"code":1,"date":"2025-08-06 06:00:52","doi":"10.21203/rs.3.rs-6781302/v1","editorialEvents":[{"type":"communityComments","content":0}],"status":"published","journal":{"display":true,"email":"[email protected]","identity":"researchsquare","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":true,"externalIdentity":"","sideBox":"","snPcode":"","submissionUrl":"/submission","title":"Research Square","twitterHandle":"researchsquare","acdcEnabled":true,"dfaEnabled":false,"editorialSystem":"","reportingPortfolio":"","inReviewEnabled":false,"inReviewRevisionsEnabled":true}}],"origin":"","ownerIdentity":"01de19fd-137d-4185-9a6a-87992ba39363","owner":[],"postedDate":"August 6th, 2025","published":true,"recentEditorialEvents":[],"rejectedJournal":[],"revision":"","amendment":"","status":"posted","subjectAreas":[{"id":49829229,"name":"Health sciences/Diseases/Infectious diseases/Malaria"},{"id":49829230,"name":"Health sciences/Health care/Health policy"},{"id":49829231,"name":"Health sciences/Health care/Public health/Epidemiology"},{"id":49829232,"name":"Health sciences/Health care/Disease prevention/Lifestyle modification"}],"tags":[],"updatedAt":"2025-08-06T06:00:52+00:00","versionOfRecord":[],"versionCreatedAt":"2025-08-06 06:00:52","video":"","vorDoi":"","vorDoiUrl":"","workflowStages":[]},"version":"v1","identity":"rs-6781302","journalConfig":"researchsquare"},"__N_SSP":true},"page":"/article/[identity]/[[...version]]","query":{"redirect":"/article/rs-6781302","identity":"rs-6781302","version":["v1"]},"buildId":"8U1c8b4HqxoKbykW_rLl7","isFallback":false,"isExperimentalCompile":false,"dynamicIds":[84888],"gssp":true,"scriptLoader":[]}

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