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Small area spatial modelling &
      mapping of health
          Dianna Smith
         11 March 2013
Research streams
 Social and spatial health inequalities in
  US, UK, NZ
 Measuring demand/access to services:
  ArcGIS
 Modelling demand/access to services: spatial
  interaction
 Filling in missing data: spatial microsimulation
  for synthetic populations
Mathur, R., Noble, D., Smith, D., Greenhalgh, T., & Robson, J. (2012). Quantifying the risk of type 2 diabetes in East
London using the QDScore: a cross-sectional analysis. British Journal of General Practice, 62(603), e663-e670.
                                                                                                                 © The authors
Spatial interaction (gravity)
                                        m m m
 Identify the relative
                                m
                             S ij    Oi Ai W j   exp(   d ij )
                                                           m

  attractiveness of a
  destination for
  segments of the
  population
 Calculate demand for
  services
   Or location-allocation
    for mobile services
Small area spatial modelling and mapping of health
Linking datasets and building estimates

 If there is a               Health data     Census
  representative              (non-spatial)   (spatial)
  population survey that      age             age
  has variables in            sex             sex
  common with a               ethnicity
  census, these variables                     ethnicity
  can be used to calculate    social grade
                                              social grade
  the probabilities of each   BMI (obesity)
  person in the survey        diabetes
  living in each area.
 If the survey includes
  data on obesity and
  diabetes for each
  person, every time a
  person is „assigned‟ to
  an area the prevalence
A good model
 The linking characteristics must be predictive of
 the health outcome for that population
   In Scotland, ethnicity is irrelevant for BMI estimation
 Helps if there is some scale where prevalence is
 known
   Aggregate the estimated data to check accuracy
 Cluster the areas with populations which are most
 similar in terms of predictive characteristics for
 the behaviour/outcome
   Global smoothing algorithm can create error in
   „unusual‟ populations
Area characteristics: clusters




Cluster
membership
   1:High % in DE, over 50
   2: Low % DE, over 50
   3: Low % DE, high % over 50



                                           ±
   4: High % non-white, % DE, % under 50
   5: High % DE, % under 50                    0   3   6   12
                                                            Kilometers
Estimated Diabetes
                                                                                    LS29                                                 LS21

                                  BD20
                                                                                                                                     LS19
                                                                                     LS20



                              BD21                                                                              LS19
                                                        BD16                                                                                LS17
                                                                               BD17                                                LS16


                                                                                                                         LS18
                                                                                                  BD10
         BD22                                                           BD18

                                                                                                                                           LS6
                                             BD15                                                                                  LS5
                                                                  BD9                        BD2
                                                                                                                            LS13
                                                                                                                                          LS4

                                                                              BD8                                                               LS3
                                                                                                               LS28
                                                                                                   BD3
                                     BD13                                            BD1
                                                                                                                                   LS12
                                                                        BD7
                                                         BD14
                                                                                BD5
                                                                                                                                            LS11
 Diabetes SIR                                                                                            BD4
 (Optimal model)                                                        BD6
      75.5 - 92.8                                                                                                 BD11
                                                                                                                                   LS27
      92.9 - 100.0



                                         ±
                                                                                    BD12
      100.1 - 150.0
      150.1 - 250.0                                                                        BD19
                      0   1   2          4          6           8
      250.1 - 350.1                                              Kilometers
Potential applications
 Building on incomplete datasets from current
  records: linking data from multiple sources
  (building on Tatem et al 2012, “Mapping
  populations at risk”
 Estimating outcomes of interventions: scenario
  modelling
Difficulties
 All very quantitative models
 Minimal applications (of the models) in
 LMICs, especially in terms of health outcomes
References
 Mathur, R., Noble, D., Smith, D., Greenhalgh, T., &
  Robson, J. (2012). Quantifying the risk of type 2
  diabetes in East London using the QDScore: a cross-
  sectional analysis. British Journal of General
  Practice, 62(603), e663-e670.
 Smith, D. M., Pearce, J. R., & Harland, K. (2011). Can
  a deterministic spatial microsimulation model provide
  reliable small-area estimates of health behaviours?
  An example of smoking prevalence in New Zealand.
  Health & Place, 17(2), 618-624.
 Tatem, A., Adamo, S., Bharti, N., Burgert, C., Castro,
  M., Dorelien, A., et al. (2012). Mapping populations at
  risk: improving spatial demographic data for infectious
  disease modeling and metric derivation. Population
  Health Metrics, 10(1), 8.

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Small area spatial modelling and mapping of health

  • 1. Small area spatial modelling & mapping of health Dianna Smith 11 March 2013
  • 2. Research streams  Social and spatial health inequalities in US, UK, NZ  Measuring demand/access to services: ArcGIS  Modelling demand/access to services: spatial interaction  Filling in missing data: spatial microsimulation for synthetic populations
  • 3. Mathur, R., Noble, D., Smith, D., Greenhalgh, T., & Robson, J. (2012). Quantifying the risk of type 2 diabetes in East London using the QDScore: a cross-sectional analysis. British Journal of General Practice, 62(603), e663-e670. © The authors
  • 4. Spatial interaction (gravity) m m m  Identify the relative m S ij  Oi Ai W j exp(   d ij ) m attractiveness of a destination for segments of the population  Calculate demand for services  Or location-allocation for mobile services
  • 6. Linking datasets and building estimates  If there is a Health data Census representative (non-spatial) (spatial) population survey that age age has variables in sex sex common with a ethnicity census, these variables ethnicity can be used to calculate social grade social grade the probabilities of each BMI (obesity) person in the survey diabetes living in each area.  If the survey includes data on obesity and diabetes for each person, every time a person is „assigned‟ to an area the prevalence
  • 7. A good model  The linking characteristics must be predictive of the health outcome for that population  In Scotland, ethnicity is irrelevant for BMI estimation  Helps if there is some scale where prevalence is known  Aggregate the estimated data to check accuracy  Cluster the areas with populations which are most similar in terms of predictive characteristics for the behaviour/outcome  Global smoothing algorithm can create error in „unusual‟ populations
  • 8. Area characteristics: clusters Cluster membership 1:High % in DE, over 50 2: Low % DE, over 50 3: Low % DE, high % over 50 ± 4: High % non-white, % DE, % under 50 5: High % DE, % under 50 0 3 6 12 Kilometers
  • 9. Estimated Diabetes LS29 LS21 BD20 LS19 LS20 BD21 LS19 BD16 LS17 BD17 LS16 LS18 BD10 BD22 BD18 LS6 BD15 LS5 BD9 BD2 LS13 LS4 BD8 LS3 LS28 BD3 BD13 BD1 LS12 BD7 BD14 BD5 LS11 Diabetes SIR BD4 (Optimal model) BD6 75.5 - 92.8 BD11 LS27 92.9 - 100.0 ± BD12 100.1 - 150.0 150.1 - 250.0 BD19 0 1 2 4 6 8 250.1 - 350.1 Kilometers
  • 10. Potential applications  Building on incomplete datasets from current records: linking data from multiple sources (building on Tatem et al 2012, “Mapping populations at risk”  Estimating outcomes of interventions: scenario modelling
  • 11. Difficulties  All very quantitative models  Minimal applications (of the models) in LMICs, especially in terms of health outcomes
  • 12. References  Mathur, R., Noble, D., Smith, D., Greenhalgh, T., & Robson, J. (2012). Quantifying the risk of type 2 diabetes in East London using the QDScore: a cross- sectional analysis. British Journal of General Practice, 62(603), e663-e670.  Smith, D. M., Pearce, J. R., & Harland, K. (2011). Can a deterministic spatial microsimulation model provide reliable small-area estimates of health behaviours? An example of smoking prevalence in New Zealand. Health & Place, 17(2), 618-624.  Tatem, A., Adamo, S., Bharti, N., Burgert, C., Castro, M., Dorelien, A., et al. (2012). Mapping populations at risk: improving spatial demographic data for infectious disease modeling and metric derivation. Population Health Metrics, 10(1), 8.