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  <front>
    <journal-meta />
    <article-meta>
      <title-group>
        <article-title>Spatio-temporal visualisation of disease incidence and respective intervention strategies</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <string-name>Dr Priscilla Rogers</string-name>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Manager IBM Research Australia</string-name>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Stefan Von Cavallar</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Matthew Davis</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Kelly L. Wyres</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Matthias Reumann</string-name>
          <xref ref-type="aff" rid="aff2">2</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Martin J. Sepulveda</string-name>
          <xref ref-type="aff" rid="aff1">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Priscilla Rogers</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <aff id="aff0">
          <label>0</label>
          <institution>IBM Research - Australia</institution>
          ,
          <addr-line>204 Lygon Street, Carlton, VIC 3053</addr-line>
          ,
          <country country="AU">Australia</country>
        </aff>
        <aff id="aff1">
          <label>1</label>
          <institution>IBM Research - Watson</institution>
          ,
          <addr-line>1101 Kitchawan Road, Yorktown Heights, NY, 10598</addr-line>
          <country country="US">USA</country>
        </aff>
        <aff id="aff2">
          <label>2</label>
          <institution>IBM Research - Zurich</institution>
          ,
          <addr-line>Saeumerstrasse 4, 8803 Rueschlikon</addr-line>
          ,
          <country country="CH">Switzerland</country>
        </aff>
      </contrib-group>
      <pub-date>
        <year>2014</year>
      </pub-date>
      <fpage>38</fpage>
      <lpage>39</lpage>
      <abstract>
        <p>SUMMARY The ability to effectively collect and leverage information offers rich new insights, which can greatly inform decision making within healthcare practice and health systems. In this study, we show how information can be collected, analysed and presented in new ways to inform key decision makers in understanding the prevalence of disease and the response to interventions. We demonstrate this for malaria, using data sources from Kenya, where malaria is one of the three biggest causes of mortality for children under the age of 5 in the sub-Saharan continent of Africa1.</p>
      </abstract>
    </article-meta>
  </front>
  <body>
    <sec id="sec-1">
      <title>-</title>
      <p>Priscilla Rogers is a Research Staff Member at IBM
Research - Australia, and the manager of the Laboratory’s
Healthcare Research team. In this role, she is responsible
for driving the research agenda in healthcare, and is
passionate about data-driven healthcare and pioneering
technologies for transformative plays in the sector. Priscilla
studied Mechanical Engineering at Monash University, and
holds a PhD in acoustic microfluidics for lab-on-a-chip
device applications, also from Monash.</p>
    </sec>
    <sec id="sec-2">
      <title>DESCRIPTION</title>
      <p>The Cognitive Healthcare and Health Systems Hub is a framework that provisions the ability to collect, store
and analyse data from many data providers in a secure manner. The visualisation portal allows relevant
bodies to obtain and visualise tailored insights into data within the Hub. This includes a portal to visualise the
disease burden of a particular disease and the potential impact of available and relevant interventions. The
portal employs a geospatial 3D environment in which to visualise data, enabling the user to view information
from a sub-county/town/house level through to a country wide overview. By further augmenting the disease
model data with information representing other entities, such as points of interest (i.e. healthcare clinics,
pharmacies etc) we can obtain a deeper insight into the disease and appropriate resources available to the
different regions.</p>
      <p>At its most basic, the disease model data is visualised by utilising a combination of D32 and Cesium3. The D3
framework is used to process the visualisation data and transform it into a form ready for presentation. The
Cesium framework is used to present the visualisation data within a geospatial 3D environment, for example
displaying sub-county boundary lines, sub-county names, points of interest etc., right through to rendering the
level of red shading within each sub-county region to represent the estimated incidence of disease. Enhanced
user functionality is provided by the framework, allowing the user to both navigate the 3D environment and
clearly see how the disease burden changes with space and time.</p>
      <p>The Spatiotemporal Epidemiological Modeler (STEM), an open source tool to simulate models of disease, was
used to generate data for an epidemic malaria outbreak and associated public health interventions in Kenya4.</p>
      <p>STEM contains a malaria disease model to simulate disease transmission by region using environmental and
earth science data sources, including elevation, temperature, precipitation, and vegetation coverage5,6.</p>
      <p>To model malaria in Kenya and integrate the intervention scenarios, we made several changes to the included models and data in STEM. First, we replaced the
default Kenya data with higher resolution political and earth science data sources, enabling simulations at sub-county resolution. Next we modified the program
to modulate disease model parameters by region. This allows us to target interventions for specific regions. For the “distribute bed nets” intervention, the malaria
model’s biting rate was modified; for “spray insecticide”, we constrain the mosquito population. To feed simulation data directly to the visualisation portal, we also
implemented a JSON data logger in STEM. Model parameters for the baseline and intervention scenarios were derived from literature.
The portal enables the user to select which scenario output to visualise. Such visualisation allows intuitive access to information essential for those interested in
understanding transmission dynamics or planning disease control strategies. Future versions could also link directly to the simulation engine, allowing scientists to
modify rate parameters real time to the simulation and actively test alternate hypotheses. Such comparisons will greatly inform public health policy-makers.</p>
    </sec>
    <sec id="sec-3">
      <title>CONCLUSION</title>
      <p>In this study, we simulate disease incidence data for various scenarios using a mathematical model for analysing and visualising the infectious disease spread in
human populations over time and over geographies. We have shown how leveraging information can be used to inform users on the prevalence of disease and the
ways in which the diseases are best treated and prevented.</p>
    </sec>
  </body>
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