OBJECTIVE

Focusing health interventions in places with suboptimal glycemic control can help direct resources to neighborhoods with poor diabetes-related outcomes, but finding these areas can be difficult. Our objective was to use indirect measures versus a gold standard, population-based A1C registry to identify areas of poor glycemic control.

RESEARCH DESIGN AND METHODS

Census tracts in New York City (NYC) were characterized by race, ethnicity, income, poverty, education, diabetes-related emergency visits, inpatient hospitalizations, and proportion of adults with diabetes having poor glycemic control, based on A1C >9.0% (75 mmol/mol). Hot spot analyses were then performed, using the Getis-Ord Gi* statistic for all measures. We then calculated the sensitivity, specificity, positive and negative predictive values, and accuracy of using the indirect measures to identify hot spots of poor glycemic control found using the NYC A1C Registry data.

RESULTS

Using A1C Registry data, we identified hot spots in 42.8% of 2,085 NYC census tracts analyzed. Hot spots of diabetes-specific inpatient hospitalizations, diabetes-specific emergency visits, and age-adjusted diabetes prevalence estimated from emergency department data, respectively, had 88.9%, 89.6%, and 89.5% accuracy for identifying the same hot spots of poor glycemic control found using A1C Registry data. No other indirect measure tested had accuracy >80% except for the proportion of minority residents, which had 86.2% accuracy.

CONCLUSIONS

Compared with demographic and socioeconomic factors, health care utilization measures more accurately identified hot spots of poor glycemic control. In places without a population-based A1C registry, mapping diabetes-specific health care utilization may provide actionable evidence for targeting health interventions in areas with the highest burden of uncontrolled diabetes.

In the U.S., diabetes prevalence has doubled over the last two decades, and now nearly 1 in 10 Americans has diabetes (1,2). However, these increases have not been evenly distributed, and some geographic regions face a substantially higher burden of diabetes (3,4). For individuals with suboptimal glycemic control, the risk of diabetes-related complications is higher, which leads to frequent hospitalizations, more health care expenditures, disability, and premature death (5,6).

To more effectively reduce the burden of diabetes-related health problems, interventions could target those geographic regions where more people with diabetes have poor glycemic control (7,8). These health interventions for diabetes could also be tailored to the specific health needs of affected communities (9,10). However, the first step is to identify the geographic areas where the proportion of people with poorly controlled diabetes is particularly high.

In New York City (NYC), the A1C Registry was created in 2006 by the NYC Department of Health and Mental Hygiene as a comprehensive collection of all A1C test results (excluding point-of-care tests) from NYC residents (11). Using address information provided with results, the A1C Registry has been used to identify geographic areas with high incidence of poor glycemic control (12,13). Identification of these areas provides potential focal points to target limited resources for improving glycemic control among adults with diabetes. Other efforts using A1C data from diabetes registries have been helpful in exploring disparities in diabetes management. Prior studies have used this data to assess barriers to care and examine the impact of the food and built environment on glycemic control (1416).

However, most of the country does not have access to a comprehensive registry of A1C values with detailed geographic data. Therefore, the objective of our study was to identify alternative data sources and measures that are more widely available to other jurisdictions. These proxies could be used as indirect measures of identifying hot spots of poor glycemic control. Existing literature has found that glycemic control varies based on race and socioeconomic status (1719). In addition, a previous study has shown that local geographic regions with higher rates of diabetes-specific emergency department use overlap with areas that have higher rates of microvascular diabetes-related complications (20).

We hypothesized that some of these measures could be used as proxies for poor glycemic control if the geographic hot spots of these factors overlapped substantially with a high prevalence of high A1C values. To test this hypothesis, we compared the accuracy of using hot spots of demographic, socioeconomic, and health care utilization data to identify hot spots of poor glycemic control.

Study Population

Our study included all unique adults identified in the NYC A1C Registry with likely diabetes (referred to as diabetes going forward) based on having an A1C of ≥6.5% (48 mmol/mol) for two or more tests (12). For health care utilization data, we included data from general, acute-care hospitals in NYC for patients who either had an inpatient hospitalization or emergency department visit and who had a diagnosis of diabetes. We excluded patients from correctional facilities and nursing homes to study the general, noninstitutionalized adult population in NYC. In addition, we excluded data from specialty hospitals (e.g., surgical subspecialty, oncology, or veterans). We only included adults residing in NYC who had a geocodable home address that matched to a NYC census tract (21).

Data Sources

We used laboratory data from the NYC A1C Registry as a gold standard for identifying areas with a high proportion of individuals with poor glycemic control (11). Data on all A1C values (regardless of the indication for the test) are electronically reported from laboratories to the NYC Department of Health and Mental Hygiene. For this study, we used A1C values from 2011 to 2013 to determine whether a person with diabetes had poor control and data from 2006 to 2013 (providing an additional 5-year look-back period) to determine whether a person in our study had diabetes based on a history of two or more A1C tests of ≥6.5% (48 mmol/mol). For sociodemographic predictors, we used the American Community Survey (ACS), which is an ongoing nationwide survey performed by the U.S. Census Bureau. It gathers data including demographic and socioeconomic characteristics. For obtaining census tract–level estimates, survey data are pooled over 5 years (22). To best match the 2011–2013 study period, we used ACS data from 2009 to 2013.

For health care utilization metrics, we used the Statewide Planning and Research Cooperative System (SPARCS) database, which is a comprehensive all-payer New York State claims database (23,24). Using data from 2011 to 2013, we calculated rates of emergency department visits, inpatient hospitalizations, and previously validated estimations of diabetes prevalence based on emergency claims data (25). To compare the study populations of adults with diabetes in the A1C Registry and SPARCS inpatient and emergency patient populations, we abstracted available data on age, sex, race/ethnicity, and health insurance status for analysis in summary statistics.

Main Outcome

Our main outcome was the identification of hot spots where the prevalence of poor glycemic control demonstrated statistically significant clustering. To calculate the prevalence of poor glycemic control using A1C Registry data, we divided the number of adults with diabetes whose most recent A1C result was >9.0% (75 mmol/mol) by the total number of adults with diabetes as determined by having two or more A1C results ≥6.5% (48 mmol/mol). An individual was considered to have poor glycemic control if his/her most recent A1C test result in the 2011–2013 study period was >9.0% (75 mmol/mol) (26). This calculation was performed for each census tract in NYC. The hot spot analysis described below was then performed to identify statistically significant clusters of poor glycemic control (20).

Predictor Variables

We analyzed the selected demographic and socioeconomic factors from the ACS, in addition to health care utilization patterns from SPARCS, to predict the geographic location of poor glycemic control hot spots (18,27). For demographic and socioeconomic characteristics, ACS data were used to calculate the proportion of non-Hispanic black, Hispanic, or minority (nonwhite or Hispanic) residents; the proportion of residents living below 100% of the federal poverty level; and the proportion of residents having less than a high school degree or equivalent. In addition, we used median household income to identify clustering of low median income.

For health care utilization patterns, we identified areas with higher rates of per capita diabetes-specific inpatient hospitalizations and emergency department visits, in addition to estimates of age-adjusted diabetes prevalence based on emergency department claims data. To create the per capita measures, we used SPARCS data for the annual number of inpatient hospitalizations and emergency department visits with a primary diagnosis (not secondary) starting with the prefix of 250 (first three numbers/letters of the code) and divided it by the total number of estimated adults from the ACS data by census tract.

We also used emergency department claims data to estimate the prevalence of diabetes among unique NYC adults who had visited an emergency department at least once during the study period (28). We divided the number of these unique NYC adults in the emergency department claims data who had ever received a primary or secondary diagnosis of diabetes (prefix 250) by the total number of unique adults who had ever visited the emergency department. This estimate was then age adjusted using four age strata (18–24, 25–44, 45–65, and ≥65 years old) and the direct method described by the Centers for Disease Control and Prevention (29). As previously published, this measure demonstrates potential to estimate the prevalence of diabetes at a smaller, more specific geographic level (28).

Statistical Analysis

To identify statistically significant hot spots of poor glycemic control and predictor variables, we used advanced geospatial clustering analysis (20). We first determined the optimal distance band for identifying the maximal spatial autocorrelation or clustering of measured values (30). To do this, we used the Getis-Ord General G statistic within fixed distance bands in 0.5-mile increments from 0.5 to 5.0 miles. Spatial weights were row standardized in this analysis to account for the nonuniform geographic distribution of NYC census tracts (31). After identifying the optimal distance band to perform our hot spot analysis, we used the Getis-Ord Gi* statistic to identify statistically significant hot spots of our main outcome and predictor variables at a 95% confidence level using a false discovery rate correction to account for multiple comparisons. A sensitivity analysis was also performed around the optimal distance band to test the influence of using smaller versus larger geographic distances to identify these hot spots.

To compare the accuracy of our predictor variables, we assessed the degree of overlap at the census tract level between poor glycemic control hot spots as identified with A1C Registry data (as the gold standard) versus hot spots for each of the predictor variables included in the study. Using 2 × 2 tables, we calculated the sensitivity [true positives/(true positives + false negatives)], specificity [true negatives/(true negatives + false positives)], positive predictive value (PPV) [true positives/(true positives + false positives)], negative predictive value (NPV) (true negatives/[false negatives + true negatives]), and overall accuracy [true positives + true negatives)/all observations] for identifying a hot spot of poor glycemic control using the hot spots of predictor variables. CIs for these statistics were determined using the binomial exact method.

To limit the influence of small cell counts, we excluded 57 census tracts that had an adult population estimate <100 for elimination of primarily nonresidential areas (e.g., parks and airports). In addition, we excluded 25 of the remaining 2,110 census tracts that had <30 unique adults in our analyses of A1C Registry data and in our estimates of age-adjusted diabetes prevalence, estimated from emergency department visit data. These exclusions were performed to reduce the influence of a few census tracts that did not have an adequate number of observations to produce reliable estimates (21).

Statistical analyses were performed in Stata 14.2 (StataCorp, College Station, TX). Geographic analysis was performed using ArcGIS Desktop 10.3.1 (Esri, Redlands, CA).

Institutional Review Board Approval

Our study protocol was approved by the institutional review boards at the New York University School of Medicine and NYC Department of Health and Mental Hygiene.

Study Population

Using the NYC A1C Registry, we identified 570,645 unique adults with diabetes, 101,643 of whom had an A1C >9.0% (75 mmol/mol). There were more adults who were between 25 and 64 years old or male in the group with poorly controlled glucose compared with all adults with diabetes (Table 1). Using emergency department claims data, we also identified 291,515 unique NYC adults with diabetes who had at least one inpatient hospitalization and 393,579 unique NYC adults with diabetes who had at least one emergency department visit. We found that the emergency department population had a slightly higher proportion of non-Hispanic black and Hispanic individuals and younger patients compared with the inpatient hospitalized population (Table 1).

Table 1

Study population characteristics for the A1C Registry and unique inpatient and emergency department patients in NYC from 2011 to 2013

NYC A1C Registry
Inpatient hospitalizationsEmergency department visits
All adults with diabetesAdults with poorly controlled diabetes
Unique adults with diabetes, n 570,645 101,643 291,515 393,579 
Age distribution (years)     
 18–24 0.3 0.7 0.8 1.3 
 25–44 9.1 15.9 8.6 11.8 
 45–64 47.4 56.6 37.9 42.0 
 ≥65 43.1 26.7 52.7 44.9 
Sex distribution     
 Male 45.7 49.3 46.2 45.1 
 Female 54.3 50.7 53.8 54.9 
Race/ethnicity distribution     
 Non-Hispanic white Not available Not available 41.7 37.2 
 Non-Hispanic black Not available Not available 30.1 32.7 
 Hispanic Not available Not available 22.1 24.3 
 Non-Hispanic Asian Not available Not available 6.1 5.8 
Health insurance status     
 Private Not available Not available 17.3 18.6 
 Medicare Not available Not available 53.1 44.4 
 Medicaid Not available Not available 26.0 26.9 
 Uninsured Not available Not available 3.6 10.1 
NYC A1C Registry
Inpatient hospitalizationsEmergency department visits
All adults with diabetesAdults with poorly controlled diabetes
Unique adults with diabetes, n 570,645 101,643 291,515 393,579 
Age distribution (years)     
 18–24 0.3 0.7 0.8 1.3 
 25–44 9.1 15.9 8.6 11.8 
 45–64 47.4 56.6 37.9 42.0 
 ≥65 43.1 26.7 52.7 44.9 
Sex distribution     
 Male 45.7 49.3 46.2 45.1 
 Female 54.3 50.7 53.8 54.9 
Race/ethnicity distribution     
 Non-Hispanic white Not available Not available 41.7 37.2 
 Non-Hispanic black Not available Not available 30.1 32.7 
 Hispanic Not available Not available 22.1 24.3 
 Non-Hispanic Asian Not available Not available 6.1 5.8 
Health insurance status     
 Private Not available Not available 17.3 18.6 
 Medicare Not available Not available 53.1 44.4 
 Medicaid Not available Not available 26.0 26.9 
 Uninsured Not available Not available 3.6 10.1 

Data are percent unless otherwise indicated.

Clustering Analysis

With use of the Getis-Ord General G statistic, maximal spatial clustering for the prevalence of high A1C values was identified within a distance band of 1.5 miles in NYC. For predictor variables, maximal spatial clustering was also identified at 1.5 miles for minority race/ethnicity, poverty, low education, low median income, and age-adjusted diabetes prevalence estimated from emergency department visit data. Maximal spatial clustering for non-Hispanic black residents and Hispanic residents and the frequency of diabetes-specific inpatient hospitalizations and emergency department visits were found at a slightly wider distance band of 2.0 miles. Given these results and slightly higher precision of a smaller distance band, we decided to map all hot spot analyses using 1.5 miles to maintain consistency in our analyses. Using A1C Registry data, we identified hot spots in 42.8% of the 2,085 NYC census tracts analyzed, with the average prevalence of poorly controlled diabetes of 20.6% in hot spots compared with 14.7% in non–hot spots.

Demographics Factors

Among demographic predictors, we found that the highest sensitivity at 83.0% was achieved by using hot spots of minority residents to identify poor glycemic control hot spots as measured by the gold standard A1C data. Specificity was 88.6% with PPV and NPV at 84.5% and 87.4%, respectively. Comparatively, hot spots of non-Hispanic black residents and hot spots of Hispanic residents were much less sensitive at 58.0% and 51.9%. However, hot spots of non-Hispanic black residents did have a higher specificity, at 91.2%, for identifying hot spots of poor glycemic control (Table 2).

Table 2

Using hot spots of health care utilization and demographic and socioeconomic factors to identify hot spots of poor glycemic control

Predictor variables clustered at 1.5 miles using hot spot analysisSensitivitySpecificityPPVNPVAccuracy
Demographic factors      
 Proportion of non-Hispanic black residents 58.0 (54.6–61.2) 91.2 (89.4–92.7) 83.1 (79.9–86.0) 74.4 (72.0–76.6) 77.0 (75.1–78.8) 
 Proportion of Hispanic residents 51.9 (48.6–55.2) 87.4 (85.4–89.3) 75.5 (71.9–78.9) 70.9 (68.5–73.2) 72.2 (70.3–74.1) 
 Proportion of minority residents 83.0 (80.3–85.4) 88.6 (86.7–90.3) 84.5 (81.9–86.8) 87.4 (85.4–89.2) 86.2 (84.6–87.6) 
Socioeconomic factors      
 Low median household income 65.9 (62.7–69.0) 79.9 (77.6–82.2) 71.1 (67.8–74.1) 75.8 (73.3–78.2) 73.9 (72.0–75.8) 
 Proportion of residents below poverty level 59.3 (56.0–62.5) 91.2 (89.4–92.7) 83.4 (80.3–86.2) 75.0 (72.7–77.2) 77.6 (75.7–79.3) 
 Proportion of residents with <high school degree or equivalent 56.4 (53.1–59.7) 81.8 (79.5–84.0) 69.9 (66.4–73.2) 71.5 (69.0–73.0) 70.9 (68.9–72.9) 
Health care utilization      
 Frequency of diabetes-specific inpatient hospitalizations 75.7 (72.7–78.5) 98.8 (98.0–99.4) 98.0 (96.6–98.9) 84.5 (82.4–86.3) 88.9 (87.5–90.2) 
 Frequency of diabetes-specific emergency visits 77.1 (74.2–79.8) 98.9 (98.1–99.4) 98.1 (96.8–99.0) 85.3 (83.3–87.1) 89.6 (88.2–90.9) 
 Estimated age-adjusted diabetes prevalence 86.5 (84.1–88.7) 91.7 (90.0–93.2) 88.6 (86.3–90.7) 90.1 (88.3–91.7) 89.5 (88.1–90.8) 
Predictor variables clustered at 1.5 miles using hot spot analysisSensitivitySpecificityPPVNPVAccuracy
Demographic factors      
 Proportion of non-Hispanic black residents 58.0 (54.6–61.2) 91.2 (89.4–92.7) 83.1 (79.9–86.0) 74.4 (72.0–76.6) 77.0 (75.1–78.8) 
 Proportion of Hispanic residents 51.9 (48.6–55.2) 87.4 (85.4–89.3) 75.5 (71.9–78.9) 70.9 (68.5–73.2) 72.2 (70.3–74.1) 
 Proportion of minority residents 83.0 (80.3–85.4) 88.6 (86.7–90.3) 84.5 (81.9–86.8) 87.4 (85.4–89.2) 86.2 (84.6–87.6) 
Socioeconomic factors      
 Low median household income 65.9 (62.7–69.0) 79.9 (77.6–82.2) 71.1 (67.8–74.1) 75.8 (73.3–78.2) 73.9 (72.0–75.8) 
 Proportion of residents below poverty level 59.3 (56.0–62.5) 91.2 (89.4–92.7) 83.4 (80.3–86.2) 75.0 (72.7–77.2) 77.6 (75.7–79.3) 
 Proportion of residents with <high school degree or equivalent 56.4 (53.1–59.7) 81.8 (79.5–84.0) 69.9 (66.4–73.2) 71.5 (69.0–73.0) 70.9 (68.9–72.9) 
Health care utilization      
 Frequency of diabetes-specific inpatient hospitalizations 75.7 (72.7–78.5) 98.8 (98.0–99.4) 98.0 (96.6–98.9) 84.5 (82.4–86.3) 88.9 (87.5–90.2) 
 Frequency of diabetes-specific emergency visits 77.1 (74.2–79.8) 98.9 (98.1–99.4) 98.1 (96.8–99.0) 85.3 (83.3–87.1) 89.6 (88.2–90.9) 
 Estimated age-adjusted diabetes prevalence 86.5 (84.1–88.7) 91.7 (90.0–93.2) 88.6 (86.3–90.7) 90.1 (88.3–91.7) 89.5 (88.1–90.8) 

Data are percent (CI).

Socioeconomic Factors

Compared with the proportion of minority residents, socioeconomic characteristics were not as accurate in identifying hot spots of poor glycemic control. The sensitivity of hot spots of low income, poverty, and low education for identifying poor glycemic control hot spots was 65.9%, 59.3%, and 56.4%, respectively. However, hot spots of poverty did demonstrate a high specificity, at 91.2%, for hot spots of poor glycemic control. The PPVs and NPVs for socioeconomic predictors were generally lower than values for the proportion of minority residents (Table 2).

Health Care Utilization

As for health care utilization patterns, the frequency of diabetes-specific inpatient hospitalizations and emergency visits had higher specificity, at 98.8% and 98.9%, for identifying hot spots of poor glycemic control. Sensitivity for these two measures was also higher than any other individual demographic or socioeconomic predictor except for the proportion of minority residents. Hot spots of age-adjusted diabetes prevalence based on emergency department claims data had slightly lower specificity, at 91.7%, than other health care utilization measures. However, hot spots of estimated age-adjusted diabetes prevalence based on emergency department surveillance had the highest sensitivity, at 86.5%, of any of the studied predictors for identifying hot spots of poor glycemic control (Table 2).

Geographic Distribution

Since the frequency of diabetes-specific emergency department visits had the highest PPV at 98.1% and overall accuracy at 89.6%, we mapped the geographic overlap of poor glycemic control hot spots based on A1C Registry data versus hot spots of diabetes-specific emergency department use (Fig. 1). Though the NPV for this measure, at 85.3%, was not the highest of all studied predictors, most of the same areas were identified in a comparison of hot spots in these maps.

Figure 1

Comparison of overlap for hot spots of high A1C prevalence and diabetes-specific emergency department use. Data shown by NYC census tract. Some areas marked as limited data owing to low population or observation counts. A: Rates of emergency department visits for a primary diagnosis of diabetes. B: Prevalence of poor glycemic control as defined by A1C >9.0% (75 mmol/mol). C: Comparison of hot spots of high A1C prevalence and emergency department use. ED, emergency department.

Figure 1

Comparison of overlap for hot spots of high A1C prevalence and diabetes-specific emergency department use. Data shown by NYC census tract. Some areas marked as limited data owing to low population or observation counts. A: Rates of emergency department visits for a primary diagnosis of diabetes. B: Prevalence of poor glycemic control as defined by A1C >9.0% (75 mmol/mol). C: Comparison of hot spots of high A1C prevalence and emergency department use. ED, emergency department.

Close modal

Sensitivity Analysis

We also analyzed the effect of changing the distance band on the sensitivity and PPVs for identifying hot spots of poor glycemic control. Increasing the distance band generally increased sensitivity for most of the predictive factors. Increasing the distance band did not have a consistent effect on PPVs and for most factors was slightly lower with a distance band of 2.5 miles. Decreasing the distance band decreased sensitivity and PPVs, which was most pronounced when we decreased the distance band to 0.5 miles. Increasing and decreasing the distance band also did not have a material effect on which factors had the highest sensitivity or PPVs (Supplementary Tables 1 and 2).

Overall, we found that hot spots of health care utilization measures had higher accuracy than demographic and socioeconomic factors for identifying hot spots with a high prevalence of poor glycemic control. Through this ecologic study, we demonstrate that some of these indirect measures can identify local hot spots of poor glycemic control.

For the greatest impact on health and to address disparities, it is critical to ensure better health intervention allocation to areas that are at greatest risk for the worst health outcomes (32). With geographically detailed data, it is possible to find these areas, which can inform how to tailor interventions that are specific to the neighborhoods with the greatest risk of diabetes-related complications (33).

The accuracy of socioeconomic factors, including median household income, the proportion of residents below the poverty level, and the proportion of residents with less than a high school degree or equivalent, ranged from 70% to 78%. Thus, hot spots of these socioeconomic measures had significantly less overlap with poor glycemic control hot spots than certain demographic factors such as the proportion of minority residents, which had an accuracy of 86%.

However, all health care utilization measures analyzed in our study demonstrated higher accuracy at 88–89% compared with the selected demographic and socioeconomic factors. Of all measures in our study, the frequency of diabetes-specific emergency department visits had the highest PPV, although the frequency of diabetes-specific inpatient hospitalizations essentially mapped the same regions. Also, estimated age-adjusted diabetes prevalence based on emergency department claims data had the highest sensitivity for identifying poor glycemic control hot spots based on A1C data. Though the A1C Registry and SPARCS data likely have divergent biases (individuals of low socioeconomic status are often less likely to have A1C values checked but are more likely to have emergency department visits), there was convergence in the identification of poor glycemic control hot spots between these two data sources.

In the existing literature of population-based studies of A1C values, a national study of 1,350 adults with diabetes from National Health and Nutrition Examination Survey (NHANES) 2007–2010 data demonstrated that poor glycemic control was more common among non-Hispanic black and Hispanic populations (18.7 and 18.8%) versus non-Hispanic white populations (10.1%) (17). The study also found that poor glycemic control was more common among those without a usual source of medical care (22.4%) or among those using hospitals or emergency departments for their health care needs (22.9%) compared with those accessing care at a clinic (15.2%) or a doctor’s office (11.2%) (17). No statistically significant or consistent pattern of association was found between poor glycemic control and education level or poverty income ratios (17).

Our study is not only consistent with prior studies of glycemic control but also provides evidence that in the absence of a population-level A1C Registry with geographically detailed data, health care utilization measures may potentially provide the best proxy for identifying local hot spots of poor glycemic control (18,27). The majority of states across the country already have a systematic process for collecting administrative data on emergency department visits and inpatient hospitalizations (34). Currently, 36 states contribute data to the State Emergency Department Databases (SEDD) and 48 states contribute data to the State Inpatient Databases (SID), both of which are coordinated by the Agency for Healthcare Research and Quality (35).

In areas where comprehensive systems to collect administrative data are not already in place, it may only be necessary to obtain data from selected health care facilities that have the highest geographic coverage of a particular region (25). As shown in a prior study, specific hospitals may be able to act as sentinel hospitals that can provide adequate health surveillance for a particular region as long as the hospital or group of hospitals have a patient population that mirrors the general population for the geographic area of interest (25).

By mapping of hot spots of diabetes-specific health care utilization, these methods have the potential to provide actionable evidence to both public health and health care institutions (36). Population health interventions can then be targeted to places with the highest burden of poor glycemic control (12). With address-level data, it is possible to find these hot spots with a higher level of geographic detail (28). However, our sensitivity analyses suggest that there may be a limit to these methods, as accuracy tends to decrease with use of very small distances.

With the constant pressure of limited resources, it is important to concentrate efforts to improve the health of adults with diabetes in areas with a higher burden of disease, which in part can be characterized by poor glycemic control (37,38). Thus, the PPVs of these indirect measures for tracking poor glycemic control hot spots may be more important if decisions are made to allocate additional resources to areas. This approach would reduce the likelihood of focusing resources in areas (false positives) that may not actually have the anticipated burden of disease. If these methods are used in areas outside of NYC, it should be noted that a higher or lower prevalence of poor glycemic control will have an effect on values for PPV and NPV.

In addition, a modeling approach that combines several predictive factors may be more accurate, though parameters of such models developed in specific cities may not be generalizable to other regions. Also, our geospatial analysis was performed on proportions, rates, and aggregated values. Though some areas may not score high on these metrics, the number of people with poor diabetes control in these areas may still be high on an absolute scale. Therefore, in areas with substantial variation in population density, it may be necessary to perform other types of clustering analyses using count data.

Furthermore, the importance of geographically identifying these poor glycemic control hot spots is important for identifying which particular communities may face a higher burden of diabetes (39). The cultural characteristics of residents in poor glycemic control hot spots could be used to tailor health interventions for diabetes to match the specific cultural context of these identified neighborhoods (40,41). Our finding that nearly half of the NYC census tracts were poor glycemic control hot spots reflects not necessarily that diabetes control is much worse in NYC but, rather, that there is substantial clustering of poor glycemic control in certain neighborhoods.

Further study is needed to understand whether our findings can be generalized to other geographic areas and when these alternative measures may fail to act as good proxies of poor glycemic control. NYC is a dense and unique urban environment with substantial demographic and socioeconomic segregation, in addition to a large undocumented population—all factors that have an impact on access to care, hospital utilization, and the likelihood of having tests like an A1C performed. The next steps in this line of research include conducting validation studies in other regions of the country and looking at the specific areas of poor glycemic control that these indirect measures may miss. These approaches have the potential to identify areas where the burden of poorly controlled diabetes is highest and direct resources to residents at higher risk for adverse diabetes-related outcomes.

Limitations

Identification of unique individuals in the A1C Registry and administrative data was based on matching algorithms that used a combination of patient variables (e.g., the SPARCS database uses the first two characters of first and last names, last four digits of social security numbers, sex, and date of birth to probabilistically match claims by the same patient). Incorrectly coded or missing data may have led to incorrect matches or double counting of individuals using the algorithms that matched visits or registry values for the same person. If individuals with diabetes or poor glycemic control were more or less likely to be double counted because of these errors, then that would have erroneously inflated or deflated the rates of diabetes or poor control. In addition, hospitals may not always accurately record diagnosis codes, although one study suggested that a diabetes diagnosis code among emergency department visits has a 95% sensitivity and 99% specificity for identifying individuals with diabetes among emergency department patients (42).

Also, we did not have race/ethnicity data on patients within the A1C Registry. Some groups may have different normal ranges for this test or have a higher prevalence of conditions (e.g., sickle cell) which may give false negative results. In NYC, we found that identification of hot spots appeared to work better in some counties compared with others, which may be due to variation in the quality of data provided by different hospitals. NYC is also a dense urban environment, and many of its census tracts contain a high number of residents. Less densely populated regions may require larger geographic units or longer time periods to obtain the counts necessary to provide an accurate analysis. Finally, our study is observational; thus, associations identified cannot be considered as evidence of causation.

Funding. This study was funded by National Institute of Diabetes and Digestive and Kidney Diseases grant K23-DK-110316 to study the geographic distribution of adults with diabetes.

The content of this article solely reflects the opinions of the authors and does not represent the official views of the NYC Department of Health and Mental Hygiene or the New York University School of Medicine.

Duality of Interest. No potential conflicts of interest relevant to this article were reported.

Author Contributions. D.C.L. researched data and wrote the manuscript. Q.J. researched data and reviewed and edited the manuscript. B.P.T., B.E., C.A.K., and K.J.K. reviewed and edited the manuscript. W.Y.W. wrote the manuscript. D.C.L. is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

1.
Zimmet
P
,
Alberti
KG
,
Magliano
DJ
,
Bennett
PH
.
Diabetes mellitus statistics on prevalence and mortality: facts and fallacies
.
Nat Rev Endocrinol
2016
;
12
:
616
622
[PubMed]
2.
NCD Risk Factor Collaboration (NCD-RisC)
.
Worldwide trends in diabetes since 1980: a pooled analysis of 751 population-based studies with 4.4 million participants [published correction appears in Lancet 2017;389:e2]
.
Lancet
2016
;
387
:
1513
1530
[PubMed]
3.
Danaei
G
,
Finucane
MM
,
Lu
Y
, et al.;
Global Burden of Metabolic Risk Factors of Chronic Diseases Collaborating Group (Blood Glucose)
.
National, regional, and global trends in fasting plasma glucose and diabetes prevalence since 1980: systematic analysis of health examination surveys and epidemiological studies with 370 country-years and 2.7 million participants
.
Lancet
2011
;
378
:
31
40
[PubMed]
4.
Beckles
GL
,
Chou
CF
.
Disparities in the prevalence of diagnosed diabetes—United States, 1999-2002 and 2011-2014
.
MMWR Morb Mortal Wkly Rep
2016
;
65
:
1265
1269
[PubMed]
5.
Palta
P
,
Huang
ES
,
Kalyani
RR
,
Golden
SH
,
Yeh
HC
.
Hemoglobin A1cand mortality in older adults with and without diabetes: results from the National Health and Nutrition Examination Surveys (1988-2011)
.
Diabetes Care
2017
;
40
:
453
460
[PubMed]
6.
Saydah
S
,
Tao
M
,
Imperatore
G
,
Gregg
E
.
GHb level and subsequent mortality among adults in the U.S
.
Diabetes Care
2009
;
32
:
1440
1446
[PubMed]
7.
Barker
LE
,
Kirtland
KA
,
Gregg
EW
,
Geiss
LS
,
Thompson
TJ
.
Geographic distribution of diagnosed diabetes in the U.S.: a diabetes belt
.
Am J Prev Med
2011
;
40
:
434
439
[PubMed]
8.
Loop MS, Howard G, de Los Campos G, et al. Heat maps of hypertension, diabetes mellitus, and smoking in the continental United States. Circ Cardiovasc Qual Outcomes 2017;10:e003350
[PubMed]
9.
Auchincloss
AH
,
Diez Roux
AV
,
Brown
DG
,
Erdmann
CA
,
Bertoni
AG
.
Neighborhood resources for physical activity and healthy foods and their association with insulin resistance
.
Epidemiology
2008
;
19
:
146
157
[PubMed]
10.
Story
M
,
Kaphingst
KM
,
Robinson-O’Brien
R
,
Glanz
K
.
Creating healthy food and eating environments: policy and environmental approaches
.
Annu Rev Public Health
2008
;
29
:
253
272
[PubMed]
11.
Chamany
S
,
Silver
LD
,
Bassett
MT
, et al
.
Tracking diabetes: New York City’s A1C Registry
.
Milbank Q
2009
;
87
:
547
570
[PubMed]
12.
Wu
WY
,
Jiang
Q
,
Di Lonardo
SS
.
Poorly controlled diabetes in New York City: mapping high-density neighborhoods
.
J Public Health Manag Pract
2018
;
24
:
69
74
13.
Chamany
S
,
Wu
W
,
Parton
H
. Diabetes and Its Complications.
Long Island City, NY
,
New York City Department of Health and Mental Hygiene
,
2013
14.
Zhang
YT
,
Mujahid
MS
,
Laraia
BA
, et al
.
Association between neighborhood supermarket presence and glycated hemoglobin levels among patients with type 2 diabetes mellitus
.
Am J Epidemiol
2017
;
185
:
1297
1303
[PubMed]
15.
Aronson
R
,
Orzech
N
,
Ye
C
,
Brown
RE
,
Goldenberg
R
,
Brown
V
.
Specialist-led diabetes registries and prevalence of poor glycemic control in type 2 diabetes: the Diabetes Registry Outcomes Project for A1C Reduction (DROP A1C)
.
Diabetes Care
2016
;
39
:
1711
1717
[PubMed]
16.
Tabaei
BP
,
Rundle
AG
,
Wu
WY
, et al
.
Associations of residential socioeconomic, food, and built environments with glycemic control in persons with diabetes in New York City from 2007-2013
.
Am J Epidemiol
2018
;
187
:
736
745
[PubMed]
17.
Ali
MK
,
McKeever Bullard
K
,
Imperatore
G
,
Barker
L
,
Gregg
EW
;
Centers for Disease Control and Prevention (CDC)
.
Characteristics associated with poor glycemic control among adults with self-reported diagnosed diabetes—National Health and Nutrition Examination Survey, United States, 2007-2010
.
MMWR Suppl
2012
;
61
:
32
37
[PubMed]
18.
Kirk
JK
,
D’Agostino
RB
 Jr
,
Bell
RA
, et al
.
Disparities in HbA1c levels between African-American and non-Hispanic white adults with diabetes: a meta-analysis
.
Diabetes Care
2006
;
29
:
2130
2136
[PubMed]
19.
Selvin
E
,
Parrinello
CM
,
Sacks
DB
,
Coresh
J
.
Trends in prevalence and control of diabetes in the United States, 1988-1994 and 1999-2010
.
Ann Intern Med
2014
;
160
:
517
525
[PubMed]
20.
Lee
DC
,
Long
JA
,
Sevick
MA
, et al
.
The local geographic distribution of diabetic complications in New York City: associated population characteristics and differences by type of complication
.
Diabetes Res Clin Pract
2016
;
119
:
88
96
[PubMed]
21.
Lee
DC
,
Doran
KM
,
Polsky
D
,
Cordova
E
,
Carr
BG
.
Geographic variation in the demand for emergency care: a local population-level analysis
.
Healthc (Amst)
2016
;
4
:
98
103
[PubMed]
22.
Spielman
SE
,
Folch
DC
.
Reducing uncertainty in the American community survey through data-driven regionalization
.
PLoS One
2015
;
10
:
e0115626
[PubMed]
23.
Quan
JM
.
SPARCS: the New York State health care data system
.
J Clin Comput
1980
;
8
:
255
263
[PubMed]
24.
New York State Department of Health. Statewide Planning and Research Cooperative System (SPARCS) [Internet], 2016. Available from https://www.health.ny.gov/statistics/sparcs/. Accessed 21 June 2017
25.
Lee
DC
,
Swartz
JL
,
Koziatek
CA
,
Vinson
AJ
,
Athens
JK
,
Yi
SS
.
Assessing the reliability of performing citywide chronic disease surveillance using emergency department data from sentinel hospitals
.
Popul Health Manag
2017
;
20
:
427
434
[PubMed]
26.
Garber
AJ
,
Abrahamson
MJ
,
Barzilay
JI
, et al
.
AACE/ACE comprehensive diabetes management algorithm 2015
.
Endocr Pract
2015
;
21
:
438
447
27.
Zhao
W
,
Katzmarzyk
PT
,
Horswell
R
, et al
.
HbA1c and lower-extremity amputation risk in low-income patients with diabetes
.
Diabetes Care
2013
;
36
:
3591
3598
[PubMed]
28.
Lee
DC
,
Long
JA
,
Wall
SP
, et al
.
Determining chronic disease prevalence in local populations using emergency department surveillance
.
Am J Public Health
2015
;
105
:
e67
e74
[PubMed]
29.
Klein
RJ
,
Schoenborn
CA
.
Age adjustment using the 2000 projected U.S. population
. In
Healthy People Statistical Notes
.
Hyattsville, MD
,
National Center for Health Statistics
,
2001
30.
Getis
A
,
Ord
JK
.
The analysis of spatial association by use of distance statistics
.
Geogr Anal
1992
;
24
:
189
206
31.
Esri. Hot Spot Analysis (Getis-Ord Gi*) (Spatial Statistics) [Internet]. Available from http://desktop.arcgis.com/en/arcmap/10.3/tools/spatial-statistics-toolbox/hot-spot-analysis.htm. Accessed 11 April 2018
32.
Bilheimer
LT
.
Evaluating metrics to improve population health
.
Prev Chronic Dis
2010
;
7
:
A69
[PubMed]
33.
Cromley
E
,
Kleinman
LC
,
Ramos
MA
, et al
.
A community-engaged approach to select geographic areas for interventions to reduce health disparities
.
Prog Community Health Partnersh
2011
;
5
:
299
305
[PubMed]
34.
Hirshon
JM
.
The rationale for developing public health surveillance systems based on emergency department data
.
Acad Emerg Med
2000
;
7
:
1428
1432
35.
Agency for Healthcare Research and Quality. Healthcare Cost and Utilization Project [Internet], 2017. Available from https://www.hcup-us.ahrq.gov/. Accessed 11 April 2018
36.
Curtis
AJ
,
Lee
WA
.
Spatial patterns of diabetes related health problems for vulnerable populations in Los Angeles
.
Int J Health Geogr
2010
;
9
:
43
[PubMed]
37.
Wrobel
JS
,
Mayfield
JA
,
Reiber
GE
.
Geographic variation of lower-extremity major amputation in individuals with and without diabetes in the Medicare population
.
Diabetes Care
2001
;
24
:
860
864
[PubMed]
38.
Tompkins
JW
,
Luginaah
IN
,
Booth
GL
,
Harris
SB
.
The geography of diabetes in London, Canada: the need for local level policy for prevention and management
.
Int J Environ Res Public Health
2010
;
7
:
2407
2422
[PubMed]
39.
Piccolo
RS
,
Duncan
DT
,
Pearce
N
,
McKinlay
JB
.
The role of neighborhood characteristics in racial/ethnic disparities in type 2 diabetes: results from the Boston Area Community Health (BACH) Survey
.
Soc Sci Med
2015
;
130
:
79
90
[PubMed]
40.
Castro
FG
,
Shaibi
GQ
,
Boehm-Smith
E
.
Ecodevelopmental contexts for preventing type 2 diabetes in Latino and other racial/ethnic minority populations
.
J Behav Med
2009
;
32
:
89
105
[PubMed]
41.
Gutierrez
J
,
Devia
C
,
Weiss
L
, et al
.
Health, community, and spirituality: evaluation of a multicultural faith-based diabetes prevention program
.
Diabetes Educ
2014
;
40
:
214
222
[PubMed]
42.
Zgibor
JC
,
Orchard
TJ
,
Saul
M
, et al
.
Developing and validating a diabetes database in a large health system
.
Diabetes Res Clin Pract
2007
;
75
:
313
319
[PubMed]
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