Abstract
Background
Area-level deprivation is associated with multiple adverse birth outcomes. Few studies have examined the mediating pathways through which area-level deprivation affects these outcomes. The objective of this study was to investigate the association between area-level deprivation and preterm birth, and examine the mediating effects of maternal medical, behavioural, and psychosocial factors.
Methods
We conducted a retrospective cohort study using national, commercial health insurance claims data from 2011, obtained from the Health Care Cost Institute. Area-level deprivation was derived from principal components methods using ZIP code-level data. Multilevel structural equation modeling was used to examine mediating effects.
Results
In total, 138,487 women with a live singleton birth residing in 14,577 ZIP codes throughout the United States were included. Overall, 5.7% of women had a preterm birth. In fully adjusted generalized estimation equation models, compared to women in the lowest quartile of area-level deprivation, odds of preterm birth increased by 9.6% among women in the second highest quartile (odds ratio (OR) 1.096; 95% confidence interval (CI) 1.021, 1.176), by 11.3% in the third highest quartile (OR 1.113; 95% CI 1.035, 1.195), and by 24.9% in the highest quartile (OR 1.249; 95% CI 1.165, 1.339). Hypertension and infection moderately mediated this association.
Conclusions
Even among commercially-insured women, area-level deprivation was associated with increased risk of preterm birth. Similar to individual socioeconomic status, area-level deprivation does not have a threshold effect. Implementation of policies to reduce area-level deprivation, and the screening and treatment of maternal mediators may be associated with a lower risk of preterm birth.
Keywords: Commercially-insured, Area-level deprivation, Preterm birth, Mediating pathways
Background
Ten percent of the four million births in the United States are preterm (birth prior to 37 weeks gestation): a rate relatively intransigent over the past four decades [1]. Preterm birth is a leading cause of infant mortality [2], and preterm infants that survive are susceptible to complications throughout the lifecourse including, respiratory, cardiovascular, and neurological disorders [3]. The consequent social, economic, and human burden is profound.
Both individual- and area-level factors are associated with an increased risk of preterm birth [3]. At the individual level these include sociodemographic characteristics, anthropometrics, infections, and behavioural and psychosocial factors. At the area level these include socioeconomic disadvantage and crime. Although studies have shown an association between area-level socioeconomic disadvantage and poorer birth outcomes, an important limitation of this research is that disadvantage has been measured with numerous indicators, thus making comparisons difficult [4]. In an attempt to create a standardized index, named the neighbourhood deprivation index, Messer and colleagues used principal components analysis to obtain one neighbourhood deprivation factor from 20 variables across seven sociodemographic domains including, education, employment, housing, occupation, poverty, racial composition, and residential stability [5].
Likewise, the neighbourhood deprivation index has been shown to be associated with poorer birth outcomes [6–10]. However, these studies were limited in scope and scale by being conducted in a small number of geographic regions, and by using vital statistics data which do not contain reliable information or information on potentially important covariates. For example, hypertension, sexually transmitted infections, and mental health conditions are underreported or not included on birth certificates [11, 12]. These limitations may affect the generalizability or conservativeness of study findings. Moreover, studies testing the mechanisms of these associations have been limited [13–16]. Proposed mediators of the association between area-level socioeconomic disadvantage and adverse birth outcomes include biologic, behavioural, psychosocial, and socioeconomic factors at the individual level, and access to goods and services at the area level [14, 17].
The objectives of this study were to examine the association between area-level deprivation and preterm birth, and to assess maternal mediators of this association in a national sample of women. We hypothesize that increasing levels of area-level deprivation will be associated with increased odds of preterm birth, and maternal factors will mediate this association. Using national, commercial health insurance claims data, this study extends the state-of-the-science in the following ways. First, no studies to date have examined the association between area-level deprivation and preterm birth among those commercially insured, despite the fact that commercial health insurance is the most common source of payment for deliveries in the United States, accounting for almost one-half of deliveries [18]. Other sources of payment include Medicaid (43.0%), self-pay or uninsured (4.1%), and other insurance (i.e., other government-funded sources or charity) (3.8%). Second, use of a large national sample of women enables us to explore heterogeneity in the association between area-level deprivation and adverse birth outcomes by geographic region of residence to inform policy making. And third, identifying mediating pathways may guide the development of interventions to prevent adverse birth outcomes.
Methods
Study design
This retrospective cohort study used national, commercial health insurance claims data obtained from the Health Care Cost Institute. A convenience sample of de-identified health care services data are provided by three of the largest health insurers (Aetna, Humana, and UnitedHealthcare) from all 50 states. Health Care Cost Institute data represent a quarter of the population with commercial insurance data [19]. Data are compliant with the Health Insurance Portability and Accountability Act, therefore this study was exempt from review by Institutional Review Boards.
Participants
The study sample was derived and variables defined using information available in claims data, that is Diagnosis Related Group (DRG) payment codes and International Classification of Diseases, Ninth Revision (ICD-9) procedure codes. Following previous research [20], we restricted analyses to women, ages 18 through 44, with a live birth that occurred in an inpatient hospital setting in 2011. These women were covered by employer-sponsored insurance for 10 months prior to childbirth, had a DRG code indicating a vaginal or cesarean delivery (765, 766, 774, or 775), and continued coverage for at least 6 weeks after delivery. To ensure a reliable analytic sample, we excluded patients with any of the following: delivery cannot be clearly identified in inpatient claims due to multiple admission records; non-continuous enrollment (i.e., missing membership records); multiple locations reported during the observation period (i.e., change in residence referenced by change in ZIP code); or event service dates that cross periods (e.g., antepartum outpatient visit with an initiation date prior to admission and an end date following discharge for the index event); multiple gestation (ICD-9 codes 651.00–651.23, 651.80–65.93, V27.2, V27.5); or medical indications justifying preterm delivery including, placenta previa (ICD-9 code 641.XX), and vasa previa (ICD-9 codes 663.51 and 663.53). Less than 5% of claims were excluded [20].
Variables
Individual-level variables
Birth outcome and maternal factors were obtained from the Health Care Cost Institute. Births were classified as preterm using the ICD-9 code 644.2, which indicates deliveries before 37 completed weeks of gestation. Age (18–24, 25–34, 35–44 years), and geographic location (state of residential address converted to one of nine United States Census Bureau divisions [21]), were considered as possible covariates, since preterm birth risk and the neighbourhood deprivation index vary by these factors [5, 7–9]. Specifically, preterm birth risk is higher at younger (less than 25 years) and older (35 years and older) ages [3]. Preterm birth risk differs by race [1], however data on race were not available. Therefore our findings may be overestimated and should be interpreted with caution. Reliable data were not available for other potential confounders such as body mass index (BMI), however BMI is a more important causal determinant of intrauterine growth restriction rather than preterm birth [22], and BMI is often controlled for in studies on low birth weight rather than preterm birth [7].
Maternal factors such as health, health behaviours, psychosocial stress, and individual socioeconomic resources have been conceptualized as mechanisms linking area-level socioeconomic disadvantage and preterm birth [13, 17, 22]. We considered maternal health (medical complications, infection, prior obstetric history, obstetric and fetal complications), health behaviours (substance use), and psychosocial stress (mental health conditions) as potential mediators. Data were not available to test mediating pathways through other maternal factors such as chronic stressors, social support, and individual socioeconomic resources. ICD-9 codes of potential mediators were based on prior research using health insurance claims data [23], which underwent clinical review by a maternal fetal medicine specialist (UM) (see Appendix for detailed list).
Area-level variables
We measured exposure to area-level deprivation using the neighbourhood deprivation index, reproducing the methods of Messer and colleagues [5]. This study used ZIP codes of women during pregnancy, which were converted to ZIP Code Tabulation Areas (ZCTA). Unlike many health insurance claims datasets which only include core-based statistical areas (county or counties associated with an urban core [24]), or 3-digit ZIP codes, our data includes 5-digit zip codes. Advantages of using ZIP codes include a large enough scale to protect personal privacy [25], and produce reliable estimates, yet a small enough size to effectively allocate health resources [26].
To compare area-level deprivation across varied geographic locations, preliminary principal component analyses were conducted separately for the nine census divisions. Census divisions are groupings of three to eight adjacent states (and the District of Columbia) that have similar socioeconomics, population characteristics, and historical development [21] (see Table 2 footnotes for the list of states in each division). Principal component analyses were conducted using data from all ZCTAs within a census division. ZCTA-level data were obtained from the 2011 five-year estimates from the American Community Survey [27]. An oblique rotation (promax) was used as the derived factors were correlated (> 0.32), however only the first factor was retained as it accounted for the largest proportion of variability.
Table 2.
Characteristic | Total N 138,487 | Preterm birth N (%) 7870 (5.7) | P valuea | |
---|---|---|---|---|
Age at delivery (years) | < 0.001 | |||
18–24 | 16,584 | 1014 (6.1) | ||
25–34 | 92,117 | 5001 (5.4) | ||
35–44 | 29,786 | 1855 (6.2) | ||
Census divisionb | < 0.001 | |||
New England | 4563 | 233 (5.1) | ||
Middle Atlantic | 18,565 | 1000 (5.4) | ||
East North Central | 22,524 | 1240 (5.5) | ||
West North Central | 10,291 | 561 (5.5) | ||
South Atlantic | 30,527 | 1876 (6.1) | ||
East South Central | 7615 | 473 (6.2) | ||
West South Central | 21,985 | 1316 (6.0) | ||
Mountain | 11,189 | 616 (5.5) | ||
Pacific | 11,228 | 555 (4.9) | ||
Medical factors | ||||
Maternal medical complication | ||||
Hypertension | Present | 14,511 | 1500 (10.3) | < 0.001 |
Absent | 123,976 | 6370 (5.1) | ||
Gestational diabetes | Present | 10,639 | 754 (7.1) | < 0.001 |
Absent | 127,848 | 7116 (5.6) | ||
Pre-existing diabetes | Present | 1753 | 240 (13.7) | < 0.001 |
Absent | 136,734 | 7630 (5.6) | ||
Anaemia | Present | 3531 | 230 (6.5) | < 0.001 |
Absent | 134,956 | 7640 (5.7) | ||
Infection | ||||
Vaginal, sexually transmitted, and systemic infections | Present | 38,485 | 2672 (6.9) | < 0.001 |
Absent | 100,002 | 5198 (5.2) | ||
Prior obstetric history | ||||
Incompetent cervix | Present | 2885 | 479 (16.6) | < 0.001 |
Absent | 135,602 | 7391 (5.5) | ||
Prior preterm birth | Present | 2674 | 576 (21.5) | < 0.001 |
Absent | 135,813 | 7294 (5.4) | ||
Poor obstetric history | Present | 5131 | 513 (10.0) | < 0.001 |
Absent | 133,356 | 7357 (5.5) | ||
Obstetric complication | ||||
Premature rupture of membranes | Present | 1717 | 178 (10.4) | < 0.001 |
Absent | 136,770 | 7692 (5.6) | ||
Fetal complication | ||||
Polyhydramnios | Present | 3417 | 279 (8.2) | < 0.001 |
Absent | 135,070 | 7591 (5.6) | ||
Mode of delivery | < 0.001 | |||
Cesarean section | 49,495 | 3371 (6.8) | ||
Vaginal | 88,992 | 4499 (5.1) | ||
Behavioural factors | ||||
Substance use (drug, alcohol, and tobacco use) | Present | 2153 | 190 (8.8) | < 0.001 |
Absent | 136,334 | 7680 (5.6) | ||
Psychosocial factors | ||||
Mental health condition (depression, anxiety, and other mental disorders) | Present | 7394 | 555 (7.5) | < 0.001 |
Absent | 131,093 | 7315 (5.6) |
aP values of bivariate associations between characteristics and preterm birth status obtained from generalized estimating equation models
b The United States census divisions are composed of the following states: New England (Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont); Middle Atlantic (New Jersey, New York, Pennsylvania); East North Central (Illinois, Indiana, Michigan, Ohio, Wisconsin); West North Central (Iowa, Kansas, Minnesota, Missouri, Nebraska, North Dakota, South Dakota); South Atlantic (Delaware, District of Columbia, Florida, Georgia, Maryland, North Carolina, South Carolina, Virginia, West Virginia); East South Central (Alabama, Kentucky, Mississippi, Tennessee); West South Central (Arkansas, Louisiana, Oklahoma, Texas); Mountain (Arizona, Colorado, Idaho, Montana, Nevada, New Mexico, Wyoming, Utah); and Pacific (Alaska, California, Hawaii, Oregon, Washington)
Variables were considered for inclusion in the index using a priori criteria: (1) variables loaded above 0.25 in any census division; and (2) lower 95% confidence limit of the variable loading was not below the median lower 95% confidence limit factor loading (0.17 in our analyses) [5]. Ninety-two variables loaded above 0.25 across the census divisions. Bootstrap analyses of 500 randomly drawn samples for each division were used to determine the 95% confidence interval of variable loadings. Forty-two of 92 lower 95% confidence limits did not extend below the absolute value of 0.17. Variables were considered for inclusion if they met these criteria in at least one division. Fourteen variables met all criteria (Table 1), and were retained for final principal component analysis, used to obtain final loadings. ZCTA-level data from all divisions were pooled in the final principal components analysis. Area-level deprivation was standardized to have a mean of zero and a standard deviation of one by dividing the index by the square of the eigenvalue. Higher deprivation values indicate higher levels of deprivation.
Table 1.
Sociodemographic domain | Variable |
---|---|
Education | % males and females with less than a high school education |
Employment | % males and females unemployed |
Housing | % housing rented % housing crowded % renter or owner costs in excess of 50% of income |
Occupation | % males in professional occupations |
Poverty | % households in poverty % female headed households with dependent children % households earning under $30,000/year % households on public assistance % households with no car |
Racial composition | % residents who were non-Hispanic blacks |
Residential stability | % in same residence since 1995 % residents 65 years and above |
Urbanization was measured using rural-urban commuting area (RUCA) codes [28]. RUCA codes are useful in public health studies because they may account for access to health care services [29]. ZIP code approximations of RUCA codes were used [30]. Primary RUCA codes of 10 were considered rural, remaining codes were considered non-rural.
Statistical methods
The final study sample included women with data on area-level deprivation and preterm birth. Data structure for the analysis was hierarchical: women at level one, areas at level two. Comparisons between unadjusted and adjusted generalized estimating equation models were used to assess for confounding. Only maternal factors diagnosed in at least 1% of the sample were considered for adjustment. We fit generalized estimating equation models to examine the association between area-level deprivation and preterm birth, accounting for similarities among women from the same ZCTA. Model one was the unadjusted model, model two was adjusted by covariates, and model three was adjusted by covariates and potential mediators. Interactions were assessed by adding a cross-product to the model. We allowed for non-linearity by categorizing area-level deprivation into quartiles, similar to previous studies [7, 8]. Other variables were used as categorical variables. A sensitivity analysis for unmeasured confounding was computed using the E-value [31]. Mediation was assessed using multilevel structural equation modeling [32]. Significance level of 0.05 was used. All P values were two-sided. Principal component analyses and generalized estimating equation models were performed with SAS software (Version 9.4, The SAS Institute Inc., Cary, NC, 2013). Multilevel structural equation modeling was conducted using Mplus (Version 7, Muthén & Muthén, Los Angeles, CA, 2017).
To minimize potential selection bias and endogeneity due to Health Care Cost Institute data not being a random sample, we assessed the effect of controlling for percentage of individuals in a state covered by commercial health insurance whose data was held by the Health Care Cost Institute in 2015, and ZIP code-level urbanization.
Results
A total of 138,494 women from 50 states and the District of Columbia met inclusion criteria for the study. Seven women were missing data on area-level deprivation and were excluded. Overall, 5.7% of women had a preterm birth (Table 2). Preterm births were more common among the youngest and oldest women, and among those residing in the Southeast. Preterm births were less common among women residing along the West and Northeastern coasts. A higher proportion of women with medical complications, infections, poor obstetric history, obstetric and fetal complications, substance use, and mental health conditions had a preterm birth compared to women without these risk factors. Preterm births were more common among women who had a cesarean section compared to a vaginal delivery.
In final analyses, 138,487 women in 14,577 areas were included. The standardized area-level deprivation index ranged from − 1.67 to 5.63. Distribution of area-level deprivation was fairly homogeneous across census divisions (Fig. 1). Overall, cut-off values were − 0.61, − 0.16 and 0.48 for the lowest (least deprived) to highest (most deprived) quartiles. Overall, the mean was 0.03, skewness was 1.3, and kurtosis was 2.3. By census division, quartile cut-off values were higher in the East South Central, South Atlantic, Pacific, and West South Central divisions. A high proportion of women in the southern, western, and Middle Atlantic census divisions resided in the most deprived areas (Appendix). Area-level deprivation was generally higher in central urban and rural areas (data not shown).
Results of generalized estimating equation models are presented in Table 3. Each increasing quartile of area-level deprivation was associated with population-averaged higher odds of preterm birth. Compared to women in the lowest quartile of area-level deprivation, women in the highest quartile of area-level deprivation had an increased odds of preterm birth in unadjusted (OR 1.33; 95% CI 1.24, 1.42), and fully adjusted analyses (OR 1.25; 95% CI 1.17, 1.34). However, the strength of associations may be overestimated due to our inability to account for race. In sensitivity analyses, the E-value for the highest compared to the lowest quartile of area-level deprivation was 1.807 (or 1.603 for the lower confidence limit). When area-level deprivation was modeled as a continuous variable, the P value for trend was < 0.001. State-level coverage of commercial health insurance at the Health Care Cost Institute and urbanization were not included in model three as these variables were not significant predictors. Analyses of effect modification of census division and urbanization were non-significant.
Table 3.
Variable | Model 1 (unadjusted) | Model 2 (minimally adjusted)a | Model 3 (fully adjusted)b | ||||||
---|---|---|---|---|---|---|---|---|---|
OR | 95% CI | P value | OR | 95% CI | P value | OR | 95% CI | P value | |
Area-level deprivation | |||||||||
Quartile 1 (least deprived) | 1.0 | 1.0 | 1.0 | ||||||
Quartile 2 | 1.112 | 1.037,1.193 | 0.003 | 1.115 | 1.039,1.196 | 0.003 | 1.096 | 1.021, 1.176 | 0.011 |
Quartile 3 | 1.152 | 1.074,1.235 | < 0.001 | 1.143 | 1.064,1.228 | < 0.001 | 1.113 | 1.035, 1.195 | 0.004 |
Quartile 4 (most deprived) | 1.328 | 1.241,1.421 | < 0.001 | 1.322 | 1.233,1.417 | < 0.001 | 1.249 | 1.165, 1.339 | < 0.001 |
a Generalized estimating equation model results controlling for age at delivery and census division
b Generalized estimating equation model results controlling for age at delivery, census division, hypertension, gestational diabetes, pre-existing diabetes, infection, incompetent cervix, poor obstetric history, premature rupture of membranes, mode of delivery, substance use, and mental health conditions
OR odds ratio, CI confidence interval
The direct association between area-level deprivation (continuous) and preterm birth was confirmed in the multilevel structural equation model (b = 0.036; P = 0.001). There was a significant indirect effect of area-level deprivation on preterm birth through hypertension (b = 0.013; P = 0.001) and infection (b = 0.010; P = 0.006) (Fig. 2 and Appendix). We did not find significant indirect effects through diabetes, substance use, mental health conditions, or other factors. Of the total effect of area-level deprivation on preterm birth, 39% was mediated (i.e., all indirect effects/all effects or 0.023/0.059). Model fit statistics indicated a reasonable fit of the model: root mean square error of approximation (RMSEA) was low (0.025), comparative fit index (CFI) was adequate (0.86), and standardized root mean square residual (SRMR) for within (0.03) and between (0.04) were low.
Discussion
Area-level deprivation is associated with an increased risk of morbidity and mortality in adulthood [33, 34]. Importantly during pregnancy, when health trajectories are often set for life, area-level deprivation is associated with an increased risk of adverse birth outcomes [35]. In this study, we observed that even among women with commercial health insurance, those that are potentially the most economically advantaged, higher area-level deprivation was associated with an increased risk of preterm birth.
Preterm birth prevalence in this population of commercially-insured women was 5.7%, almost half the national preterm birth rate in 2011 (11.7%) [1]. This was consistent with other studies showing that women with commercial health insurance were less likely to have a preterm birth than women with Medicaid [3]. The range of area-level deprivation index values in this national study were wider (− 1.67 to 5.63) than that found in eight geographic areas in the United States (− 1.85 to 3.72) [5]. However, quartile cut-off values were less extreme in this study (− 0.61, − 0.16 and 0.48 for quartiles one, two and three, respectively) compared to those found by others (− 0.81, − 0.173, and 0.76 for quartiles one, two and three, respectively) [5].
Among commercially-insured women, we observed an increasing trend in the odds of preterm birth as area-level deprivation increased. Note that our findings should be interpreted with caution due to our inability to account for race. Similar to studies examining the association between individual socioeconomic status and health [36], a threshold effect for area-level deprivation was not observed. On average, there was a 25% increase in the odds of preterm birth among women residing in the highest compared to the lowest quartile of area-level deprivation. This estimate may be conservative as we controlled for potential mediators. The effect size of area-level deprivation on preterm birth in our study was similar in magnitude to other studies [7, 8]. Furthermore, in a meta-analysis of seven studies on neighbourhood deprivation measured as a single measure or an index, odds ratios were significantly increased for preterm birth in the most compared to the least deprived neighbourhood quintile (OR 1.23) [35].
Our research adds to these findings by assessing if the association between area-level deprivation and preterm birth is mediated by maternal factors. We found that only hypertension and infection moderately mediated this association. Meng and colleagues showed that approximately 25% of the association between area-level socioeconomic disadvantage and preterm birth and low birthweight was mediated by individual-level factors, with socioeconomic status-related support having the highest level of mediation followed by biologic, behavioural, and psychosocial factors [13]. Schempf and colleagues found that psychosocial mediators reduced the effect of neighbourhood risk on birthweight by 12%, and behavioural mediators reduced the effect by an additional 30% to the point where neighbourhood risk was no longer statistically significant [16]. Meanwhile, area-level factors such as the density of retail outlets for alcohol, tobacco, and unhealthy and healthy foods were unlikely to mediate the association between area-level socioeconomic disadvantage and adverse birth outcomes [14]. However, area-level socioeconomic disadvantage may be associated with other adverse area-level conditions such as inadequate housing and transportation, and violence, which may influence pregnancy through psychological stress [37].
Strengths and limitations
Strengths of this study included a large sample of commercially-insured women from all 50 states and the District of Columbia, and the availability of potential mediators of the association between area-level deprivation and preterm birth. There is limited research on this association among women with commercial health insurance, who account for almost half of all births [18]. The proportion of births covered by commercial health insurance, particularly after the implementation of the Affordable Care Act (ACA), is growing [38, 39]. This study showed that despite access to commercial health insurance coverage, women who resided in areas with higher deprivation were at greater odds of preterm birth.
Limitations of the study include lack of data on important risk factors for preterm birth (e.g., race and individual socioeconomic status), operationalization of area, area and covariate/mediator misclassification, selection bias, and potential inability to generalize to women without commercial health insurance or residential stability, or women whose commercial health insurers are not included in the Health Care Cost Institute data.
Race is an important predictor of preterm birth, with non-Hispanic black women having a 60% higher prevalence of preterm birth compared to non-Hispanic white women [1]. Other studies show that among women with commercial health insurance, 66.1% are non-Hispanic white, 12.2% are non-Hispanic black, 13.3% are Hispanic, and 8.4% are non-Hispanic other race [40]. Our study population may likewise have a high composition of non-Hispanic white women which may in part explain the low prevalence of preterm birth that was observed. Differences by race/ethnicity were not able to be assessed, therefore our findings may be overestimated. In sensitivity analyses, the minimum strength of an association that an unmeasured confounder would need to have, conditional on measured covariates, to explain away the observed association of the highest compared to the lowest quartile of area-level deprivation was 1.807 (or 1.603 for the lower confidence limit). In a previous study examining neighbourhood deprivation, the adjusted relative risk of preterm birth among non-Hispanic black women compared to non-Hispanic white women was 1.4 (95% CI 1.3–1.6) [41]. This relative risk is less than our E-value which suggests that controlling for race in our analyses would likely not explain away this observed association. However, it may explain away the association for other quartile comparisons. Additionally, results from other studies indicate that adjusting for individual confounders other than race may lead to attenuation of area-level associations [7].
We cannot rule out the possibility that the associations observed in this study could be explained by residual confounding from area-level factors. Although, as indicated above an unmeasured confounder would need to have a relative risk of 1.807 or a lower confidence limit of 1.603 to explain away our observed results. The association between area-level deprivation and preterm birth may be confounded by differences in availability and quality of health care services within an area, which was beyond the scope of the data available. Insurance coverage does not indicate equal access and use of medical care [42]. Furthermore, racial differences in adverse birth outcomes are related to the quality of care at the site of delivery [43].
Areas were operationalized using ZIP codes. ZIP codes are established by the United States Postal Service as mail routes for efficient mail delivery. ZIP codes have a large population size with an average of 30,000 residents and may be socioeconomically heterogeneous [44]. In contrast, census tracts, a common operationalization of neighbourhoods used in public health research, are relatively socioeconomically homogenous statistical subdivisions of counties derived by the United States Census Bureau that have an average of 4000 residents and approximately 1000 to 3000 housing units [21]. Krieger and colleagues compared the associations between socioeconomic measures at the census block group (aggregated census blocks (subdivisions of census tracts) that have approximately 250 to 550 housing units [21]), census tract, and ZIP code level, and birthweight [45]. Measures at the census block group and census tract level showed similar associations, while ZIP-code level measures detected smaller associations. These effect sizes were similar to the effect sizes observed in our study (OR range from 1.27 to 2.17). Therefore, the magnitude of effect size using ZIP code-level data may be smaller, nonetheless significant associations still were detected. Misclassification of areas may arise as ZCTAs (aggregated census blocks that approximate ZIP Codes [46]) and ZIP codes sharing the same code may not cover exactly the same geographic area [44].
Maternal factors and outcomes were obtained from commercial health insurance claims data and their accuracy is dependent on institutional and individual coding. The positive predictor value of chronic conditions and birth outcomes for administrative health plans range from 87 to 95% [47]. Non-differential misclassification of exposures and outcomes would bias our results towards the null, therefore our observed associations could be conservative estimates.
Our study included women with commercial health insurance and residential stability. While the majority of women (53%) in the United States have stable commercial health insurance coverage during pregnancy, women who are less likely to have stable commercial health insurance are younger, non-Hispanic white, have lower socioeconomic status, and initiate prenatal care late [48]. Many of these same factors are associated with residential mobility during pregnancy [49], and preterm birth [3]. Selection bias may have led to an underselection of women with low socioeconomic status who may have had a higher risk of preterm birth. Individual-level socioeconomic status data were not available in this study, thus the direction of bias is unknown.
Our results may or may not generalize to the populations of other insurers, as we were unable to determine how individuals included in the Health Care Cost Institute data compare to individuals covered by other insurers. However, our results are internally valid. Whether the results of this study generalize to all pregnant women, particularly after the implementation of the ACA, is unknown. However, studies that take insurance status into account, still find an association between area-level deprivation and adverse birth outcomes [6].
Implications for practice and/or policy
We found that area-level deprivation was associated with increased risk of preterm birth among commercially insured women and medical factors mediated this association. The implementation of the ACA was associated with a decrease in being uninsured, and an increase in being commercially insured and receiving timely prenatal care among young women [50]. Thus, efforts to repeal the ACA may result in poorer access to prenatal care and poorer management of medical factors that mediate the association between area-level deprivation and preterm birth, particularly among young women who are at increased risk of preterm birth [3].
Our findings also suggest potential avenues for policy solutions, such as implementing policies to reduce area-level deprivation, and enabling insurers, employers, and health care providers to work towards designing care paths to address medical mediating factors, particularly hypertension and infection.
Conclusions
Our study showed that in a national sample of commercially-insured women there was notable variation in the area-level deprivation index. Even among this commercially-insured population, there were area-level socioeconomic differences that were related to the health and well-being of mothers and their infants. To reduce the risk of adverse birth outcomes such as preterm birth, it is important to identify both modifiable risk factors and mediators that are potential targets for intervention. Future research should continue to test for mediating pathways between area-level deprivation and preterm birth to determine if hypertension and infection are consistently found to mediate this association, or if there are other important mediating factors. Additional mediating factors to explore include maternal factors such as stress, and area-level conditions such as crime or material and social resources. Longitudinal study designs will enable researchers to consider causal inferences on the effects of area-level factors on preterm birth and other adverse maternal and child health outcomes.
Acknowledgements
The authors acknowledge the assistance of the Health Care Cost Institute and its data contributors, Aetna, Humana, and UnitedHealthcare in providing the claims data analysed in this study.
Funding
This work was supported by the United States Health Resources & Services Administration (grant number R40MC28308); RM was supported by the National Institutes of Health (grant number 5T32HS017589–10) and the Herman Fellowship, Yale School of Public Health; CH was supported by the National Institutes of Health (grant number 2T32HS022242–06).
Availability of data and materials
The data that support the findings of this study are available from the Health Care Cost Institute but restrictions apply to the availability of these data, which were used under license for the current study. The data are available from the Health Care Cost Institute for a licensing fee per its data use terms and conditions.
Abbreviations
- ACA
Affordable Care Act
- BMI
Body mass index
- CFI
Comparative fit index
- CI
Confidence interval
- DPR
Area-level deprivation
- DRG
Diagnosis Related Group
- EN Central
East North Central
- ES Central
East South Central
- HTN
Hypertension
- ICD-9
International Classification of Diseases, Ninth Revision
- INF
Infection
- Mid Atl
Middle Atlantic
- New Engl
New England
- OR
Odds ratio
- PTB
Preterm birth
- RMSEA
Root mean square error of approximation
- RUCA
Rural-urban commuting area
- South Atl
South Atlantic
- SRMR
Standardized root mean square residual
- WN Central
West North Central
- WS Central
West South Central
- ZCTA
ZIP Code Tabulation Area
Appendix
Table 4.
Condition | ICD-9/ DRG code | Definition |
---|---|---|
Medical factors | ||
Maternal medical complication | ||
Hypertension (including preeclampsia and eclampsia) | 401.XX | Essential hypertension |
402.XX | Hypertensive heart disease | |
403.XX | Hypertensive kidney disease | |
404.XX | Hypertensive heart and kidney disease | |
405.XX | Secondary hypertension | |
642.XX | Hypertension complicating pregnancy childbirth and the puerperium | |
Gestational diabetes | 648.00 | Diabetes mellitus complicating pregnancy childbirth or the puerperium |
648.01 | Diabetes mellitus of mother with delivery | |
648.02 | Diabetes mellitus of mother with delivery with postpartum complication | |
648.03 | Antepartum diabetes mellitus | |
648.04 | Postpartum diabetes mellitus | |
648.8 | Abnormal glucose tolerance of mother complicating pregnancy childbirth or the puerperium | |
648.80 | Abnormal glucose tolerance of mother complicating pregnancy childbirth or the puerperium unspecified as to episode of care | |
648.81 | Abnormal glucose tolerance of mother with delivery | |
648.82 | Abnormal glucose tolerance of mother with delivery with postpartum complication | |
648.83 | Abnormal glucose tolerance of mother antepartum | |
648.84 | Abnormal glucose tolerance of mother postpartum | |
Pre-existing diabetes | 250.XX | Diabetes mellitus |
Obesity | 649.1X | Obesity complicating pregnancy, childbirth, or the puerperium |
649.2X | Bariatric surgery status complicating pregnancy, childbirth, or the puerperium | |
278.XX | Overweight, obesity and other hyperalimentation | |
V85.3X | Adult body mass index ≥30.0 and ≤40.9 | |
V85.4X | Adult body mass index ≥40.0 | |
Anemia | 280 | Iron deficiency anemia |
281 | Nutritional deficiency anemia | |
285.2 | Anemia in chronic disease and neoplastic disease | |
285.9 | Anemia unspecified | |
648.2X | Anemia of mother | |
Cholestasis | 646.7X | Liver and biliary tract disorders in pregnancy, antepartum condition or complication |
Periodontal disease | 523.XX | Gingival and periodontal diseases |
IVF | V2385 | Pregnancy resulting from assisted reproductive technology |
Infection | ||
Bacteriuria | 646.5X | Asymptomatic bacteriuria in pregnancy |
791.9 | Bacteriuria | |
Systemic infection | 486 | Pneumonia organism unspecified |
540.X | Acute appendicitis | |
590.XX | Pyelonephritis or infection of kidney unspecified | |
Other infections including genital tract infections and STIs | 041.0X | Streptococcus infection |
041.5 | Hemophilus influenzae (H. influenzae) infection in conditions classified elsewhere and of unspecified site | |
041.8X | Other specified bacterial infections | |
042.XX | Human immunodeficiency virus (HIV) | |
052.XX | Chickenpox | |
053.XX | Herpes zoster | |
054.XX | Herpes simplex | |
056.XX | Rubella | |
070 | Viral hepatitis | |
070.0 | Viral hepatitis a with hepatic coma | |
070.1 | Viral hepatitis a without hepatic coma | |
070.2 | Viral hepatitis b with hepatic coma | |
070.20 | Viral hepatitis b with hepatic coma acute or unspecified without hepatitis delta | |
070.21 | Viral hepatitis b with hepatic coma acute or unspecified with hepatitis delta | |
070.3 | Viral hepatitis b without mention of hepatic coma | |
070.30 | Viral hepatitis b without hepatic coma acute or unspecified without hepatitis delta | |
070.31 | Viral hepatitis b without hepatic coma acute or unspecified with hepatitis delta | |
075.XX | Infectious mononucleosis | |
078.5 | Cytomegaloviral disease | |
079.53 | Human immunodeficiency virus type 2 [HIV-2] | |
079.83 | Parvovirus b19 | |
090.XX | Congenital syphilis | |
091.XX | Syphilis | |
092.XX | Early syphilis, latent | |
093.XX | Cardiovascular syphilis | |
094.XX | Neurosyphilis | |
095.XX | Other forms of syphilis with symptoms | |
096.XX | Late syphilis, latent | |
097.XX | Other and unspecified late syphilis | |
098.XX | Gonococcal infection | |
099.XX | Venereal disease due to chlamydia | |
130.XX | Toxoplasmosis | |
131.XX | Trichomoniasis | |
599.0 | Urinary tract infection site not specified | |
616.1X | Bacterial vaginosis | |
646.6X | Infections of genitourinary tract | |
647.60 | Other viral diseases of mother complicating pregnancy childbirth or the puerperium unspecified as to episode of care | |
647.61 | Other viral diseases of mother with delivery | |
647.62 | Other viral diseases of mother with delivery with postpartum complication | |
647.63 | Other antepartum viral diseases | |
647.64 | Other postpartum viral diseases | |
771.1 | Congenital cytomegalovirus infection | |
795.71 | Nonspecific serologic evidence of human immunodeficiency virus (HIV) | |
V08 | Asymptomatic human immunodeficiency virus (HIV) infection status | |
Prior obstetric history | ||
Cervical incompetence | 654.5x | Cervical incompetence |
Previous preterm labor | V23.41 | Pregnancy with history of pre-term labor |
Poor obstetric history | V23.49 V23.5 | Pregnancy with other poor obstetric history Supervision of high-risk pregnancy with other poor obstetric history |
Obstetric complication | ||
Hemorrhage | 656.00 | Fetal-maternal hemorrhage unspecified as to episode of care in pregnancy |
656.01 | Fetal-maternal hemorrhage with delivery | |
656.03 | Fetal-maternal hemorrhage antepartum condition or complication | |
Premature rupture of membranes | 658.1X | Premature rupture of membranes |
658.20 | Delayed delivery after spontaneous or unspecified rupture of membranes unspecified as to episode of care | |
658.21 | Delayed delivery after spontaneous or unspecified rupture of membranes delivered | |
658.23 | Delayed delivery after spontaneous or unspecified rupture of membranes antepartum | |
Fetal complication | ||
Polyhydramnios | 657.XX | Polyhydramnios |
Fetal growth | 656.50 | Poor fetal growth affecting management of mother unspecified as to episode of care |
656.51 | Poor fetal growth affecting management of mother delivered | |
656.53 | Poor fetal growth affecting management of mother and antepartum condition or complication | |
Mode of delivery | ||
Cesarean section | DRG765 | Cesarean section w cc/mc |
DRG766 | Cesarean section w/o cc/mc | |
Vaginal | DRG774 | Vaginal delivery w complicating diagnoses |
DRG775 | Vaginal delivery w/o complicating diagnoses | |
Behavioural factors | ||
Substance use (drugs, alcohol, and tobacco) | 303.XX | Acute alcoholic intoxication or other and unspecified alcohol dependence |
304.XX | Drug dependence | |
305.XX | Nondependent abuse of drugs | |
648.33 | Antepartum drug dependence | |
649.0X | Tobacco use disorder complicating pregnancy, childbirth, or the puerperium | |
Psychosocial factors | ||
Mental health condition | 290.1X | Presenile dementia |
290.4X | Vascular dementia | |
291.XX | Alcohol withdrawal and alcohol-induced mental disorders | |
292.XX | Drug withdrawal and drug-induced mental disorders | |
293.XX | Delirium and psychotic, mood, anxiety and transient mental disorders | |
294.XX | Amnestic disorder, dementia, and other persistent mental disorders | |
295.XX | Schizophrenia | |
296.XX | Bipolar, manic affective, major depressive and episodic mood disorders | |
297.X | Paranoid state, delusional, paraphrenia and shared psychotic disorders | |
298.X | Depressive type psychosis, excitative type psychosis, reactive confusion, acute paranoid reaction, psychogenic paranoid psychosis, other and unspecified reactive psychosis and unspecified psychosis | |
299.XX | Autistic disorder, childhood disintegrative disorder, other or unspecified pervasive developmental disorder | |
300.XX | Anxiety state unspecified, panic disorder without agoraphobia, generalized anxiety disorder, other anxiety states, hysteria unspecified, conversion disorder, dissociative amnesia, dissociative fugue, dissociative identity disorder, dissociative disorder or reaction unspecified, factitious disorder with predominantly psychological signs and symptoms, other and unspecified factitious illness, phobia unspecified, agoraphobia with panic disorder, agoraphobia without panic attacks, social phobia, other isolated or specific phobias, obsessive-compulsive disorders, dysthymic disorder, neurasthenia, depersonalization disorder, hypochondriasis, somatization disorder, undifferentiated somatoform disorder, other somatoform disorders, unspecified nonpsychotic mental disorder | |
301.XX | Paranoid personality disorder, affective personality disorder unspecified, chronic hypomanic personality disorder, chronic depressive personality disorder, cyclothymic disorder, schizoid personality disorder unspecified, introverted personality, schizotypal personality disorder, explosive personality disorder, obsessive-compulsive personality disorder, histrionic personality disorder unspecified, chronic factitious illness with physical symptoms, other histrionic personality disorder, dependent personality disorder, antisocial personality disorder, narcissistic personality disorder, avoidant personality disorder, borderline personality disorder, passive-aggressive personality, other personality disorders, unspecified personality disorder | |
302.XX | Unspecified psychosexual disorder | |
317 | Mild intellectual disabilities | |
318.X | Moderate, severe and profound intellectual disabilities | |
319 | Unspecified intellectual disabilities | |
648.4X | Mental disorders of mother |
DRG Diagnosis Related Group, HIV human immunodeficiency virus, ICD-9 International Classification of Diseases, Ninth Revision, IVF in vitro fertilization, STI sexually transmitted infection
Table 5.
Census divisiona | Area-level deprivation (quartiles) N (%) | Total N 138,487 | |||
---|---|---|---|---|---|
1 (least deprived) | 2 | 3 | 4 (most deprived) | ||
New England | 1826 (40.0) | 1018 (22.3) | 809 (17.7) | 910 (19.9) | 4563 |
Middle Atlantic | 5982 (32.2) | 4211 (22.7) | 2187 (11.8) | 6185 (33.3) | 18,565 |
East North Central | 6918 (30.7) | 5850 (26.0) | 5445 (24.2) | 4311 (19.1) | 22,524 |
West North Central | 3980 (38.7) | 2804 (27.2) | 2233 (21.7) | 1274 (12.4) | 10,291 |
South Atlantic | 5052 (16.5) | 7847 (25.7) | 8872 (29.1) | 8756 (28.7) | 30,527 |
East South Central | 1274 (16.7) | 1590 (20.9) | 2714 (35.6) | 2037 (26.7) | 7615 |
West South Central | 5152 (23.4) | 4680 (21.3) | 6159 (28.0) | 5994 (27.3) | 21,985 |
Mountain | 3016 (27.0) | 3084 (27.6) | 2907 (26.0) | 2182 (19.5) | 11,189 |
Pacific | 1401 (12.5) | 3316 (29.5) | 3429 (30.5) | 3082 (27.4) | 11,228 |
a The United States census divisions are composed of the following states: New England (Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont); Middle Atlantic (New Jersey, New York, Pennsylvania); East North Central (Illinois, Indiana, Michigan, Ohio, Wisconsin); West North Central (Iowa, Kansas, Minnesota, Missouri, Nebraska, North Dakota, South Dakota); South Atlantic (Delaware, District of Columbia, Florida, Georgia, Maryland, North Carolina, South Carolina, Virginia, West Virginia); East South Central (Alabama, Kentucky, Mississippi, Tennessee); West South Central (Arkansas, Louisiana, Oklahoma, Texas); Mountain (Arizona, Colorado, Idaho, Montana, Nevada, New Mexico, Wyoming, Utah); and Pacific (Alaska, California, Hawaii, Oregon, Washington)
Table 6.
Nonstandardized estimates | Standardized estimates | |||
---|---|---|---|---|
b (SE) | P value | β (SE) | P value | |
Area level | ||||
Preterm regressed on | ||||
Hypertension | 0.263 (0.077) | 0.001 | 0.400 (0.117) | 0.001 |
Infection | 0.102 (0.037) | 0.006 | 0.230 (0.085) | 0.007 |
Deprivation (direct effect) | 0.036 (0.008) | <0.001 | 0.288 (0.076) | <0.001 |
Hypertension regressed on deprivation | 0.048 (0.006) | <0.001 | 0.249 (0.030) | <0.001 |
Infection regressed on deprivation | 0.100 (0.005) | <0.001 | 0.351 (0.017) | <0.001 |
Indirect effects | ||||
Deprivation-hypertension-PTB | 0.013 (0.004) | 0.001 | - | - |
Deprivation-infection-PTB | 0.010 (0.004) | 0.006 | - | - |
All indirect effects | 0.023 (0.006) | <0.001 | - | - |
All effects | 0.059 (0.006) | <0.001 | - | - |
Individual level | ||||
Preterm birth regressed on | ||||
Hypertension | 0.194 (0.009) | <0.001 | 0.190 (0.009) | <0.001 |
Infection | 0.082 (0.008) | <0.001 | 0.081 (0.008) | <0.001 |
Authors’ contributions
RM, SDC, and JRI conceived the study. RM conducted the literature search and wrote the first and successive drafts of the manuscript. EB and CH contributed to preparation of the data set. RM, FMS, SDC, UM, KK, and JRI contributed to study design. RM conducted the principal components analysis with input from FMS. FMS modelled and analysed the data with input from RM. All authors contributed to the interpretation of data and revised the manuscript critically for important intellectual content. All authors read and approved the final manuscript.
Ethics approval and consent to participate
Data are compliant with the Health Insurance Portability and Accountability Act, therefore this study was exempt from review by Institutional Review Boards.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data that support the findings of this study are available from the Health Care Cost Institute but restrictions apply to the availability of these data, which were used under license for the current study. The data are available from the Health Care Cost Institute for a licensing fee per its data use terms and conditions.