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Original Research

Psychiatric comorbidity and Healthcare Effectiveness Data and Information Set (HEDIS) measures of alcohol and other drug treatment initiation and engagement across 7 health care systems

, PhDORCID Icon, , PhD, , PhD, , MS, , PsyD, , PhD, MS, , PhD, MPH, , PhD, MPH, MSW, , MD, PhD, , MD, MPH, MS, , DrPH, MSW & , PhD, LMSW show all

Abstract

Background: Psychiatric comorbidity is common among patients with alcohol and other drug (AOD) use disorders. To better understand how psychiatric comorbidity influences AOD treatment access in health care systems, the present study examined treatment initiation and engagement among a large, diverse sample of patients with comorbid psychiatric and AOD use disorders. Methods: This study utilized data from a multisite observational study examining Healthcare Effectiveness Data and Information Set (HEDIS) measures of initiation and engagement in treatment (IET) among patients with AOD use disorders from 7 health care systems. Participants were aged 18 or older with at least 1 AOD index diagnosis between October 1, 2014, and August 15, 2015. Data elements extracted from electronic health records and insurance claims data included patient demographic characteristics, ICD-9 (International Classification of Diseases, Ninth Revision) diagnostic codes, and procedure codes. Descriptive analyses and multivariate logistic regression models were used to examine the relationship between patient-level factors and IET measures. Results: Across health care systems, out of a total of 86,565 patients who had at least 1 AOD index diagnosis during the study period, 66.2% (n = 57,335) patients also had a comorbid psychiatric disorder. Among patients with a comorbid psychiatric disorder, 34.9% (n = 19,998) initiated AOD treatment, and of those, 10.3% (n = 2,060) engaged in treatment. After adjusting for age, sex, and race/ethnicity, patients with comorbid psychiatric disorders were more likely to initiate (odds ratio [OR] = 3.20, 95% confidence interval [CI] = 3.08, 3.32) but no more likely to engage (OR = 0.56, 95% CI = 0.51, 0.61) in AOD treatment, compared with those without a comorbid psychiatric disorder. Conclusions: Findings suggest that identification of comorbid psychiatric disorders may increase initiation in AOD treatment. However, innovative efforts are needed to enhance treatment engagement both generally and especially for individuals without diagnosed psychiatric conditions.

Introduction

Psychiatric comorbidity is common among patients with alcohol and other drug (AOD) use disorders. Results from the 2015 National Survey on Drug Use and Health (NSDUH) estimate that of the 20.8 million people who met criteria for an AOD use disorder during the past year, about 13% had both an alcohol use and another substance use disorder, and 41% met criteria for a psychiatric disorder.Citation1 Notably, among patients with AOD use disorders, the presence of a co-occurring psychiatric disorder can influence both initiation and engagement in AOD treatment.Citation2–5 For example, in nationally representative survey samples, although individuals with alcohol use disorders were more likely to receive mental health care than AOD treatment,Citation3,Citation4 psychiatric comorbidity increased the odds of receiving AOD treatment,Citation2–4 in part because these individuals accessed integrated treatment addressing both mental health and AOD use problems.Citation3,Citation4 Identifying patient-level factors—such as the presence of psychiatric comorbidity—that can impact AOD treatment initiation and engagement is critical to improving system-level processes to address gaps between treatment need and receipt.

Health care systems are now required to measure AOD treatment initiation and engagement using the Healthcare Effectiveness Data and Information Set (HEDIS) AOD Initiation and Engagement in Treatment (IET) performance measures.Citation6,Citation7 However, very few studies have examined to what extent patient AOD care meets these standards for those with comorbid psychiatric disorders. One study of Veterans Health Administration patients found that 20% of eligible patients with co-occurring psychiatric and AOD use disorders initiated AOD treatment, and 60% of those who initiated engaged in treatment.Citation8 However, this study did not examine whether patients with comorbid psychiatric and AOD disorders were more likely to access AOD treatment compared with those without a comorbid psychiatric disorder, nor did it examine factors associated with AOD treatment initiation and engagement among patients with a comorbid psychiatric disorder.

Among patients diagnosed with AOD use disorder and comorbid psychiatric disorders, previous studies have identified several patient characteristics that may influence AOD treatment initiation and engagement, including age,Citation9 gender,Citation9–13 type and severity of comorbid psychiatric disorder,Citation4,Citation10 and presence of multiple AOD use disorders.Citation5 In a sample of older adults, patients who initiated treatment had more severe symptoms of AOD abuse and depression, compared with patients who did not initiate treatment.Citation14 Among a sample of patients with both severe mental illnesses and AOD use disorders, women were more likely to initiate treatmentCitation10 and patients with severe mental illness, such as schizophrenia, were less likely to initiate treatment.Citation10 In another sample of patients with co-occurring AOD and psychiatric disorders seeking private residential treatment, women were more likely to remain in treatment.Citation9 Among men, older age was also associated with treatment retention.Citation9 A study utilizing a nationally representative sample of US adults found that those with multiple past-year AOD use disorders were more likely to have comorbid mood or personality disorders and were less likely to seek treatment.Citation5 Thus, based on the limited literature in this area, it appears that women and older adults may be more likely than other subgroups to access AOD care and to remain in treatment, whereas those with multiple AOD use disorders may be less likely to utilize treatment. Overall, although previous studies have endeavored to better understand patient-level factors associated with AOD treatment initiation and engagement for patients with comorbid psychiatric disorders, there remain gaps in the literature. In particular, previous study samples have not included large or diverse patient populations.

Understanding how psychiatric comorbidity is related to accessing AOD treatment in health care systems could help to identify patients most and least likely to initiate and engage in care. A better understanding of care patterns may also inform approaches to supporting patients in need of critical services. The primary aim of the present study was to determine whether psychiatric comorbidity may influence service utilization outcomes based on HEDIS AOD IET measures. We hypothesized that among patients with an AOD diagnosis, those with a comorbid psychiatric disorder diagnosis in the year prior to the index AOD diagnosis would be more likely to both initiate and engage in AOD treatment than those with AOD diagnosis only. We also examined the effects of specific psychiatric disorders, including anxiety, depression, and psychosis, as well as prior AOD use disorders (given the high level of comorbidity typically observed within AOD use disordersCitation15,Citation16), on initiation and engagement.

Methods

The present study used health care system data from a multisite study (National Institute on Drug Abuse [NIDA] CTN-0072-OT: Examine Patient and System-Level Factors Associated with HEDIS AOD-IET Measure Performance across Health Systems) examining HEDIS AOD IET measures among patients with an index AOD diagnosis assigned between October 1, 2014, and August 15, 2015. Seven health care systems in the Health Systems Node of the National Drug Abuse Treatment Clinical Trials Network (CTN) participated in the main study (5UG1DA040314-03). These systems have diverse geographic, patient demographic, and organizational characteristics. All health care systems shared a common Virtual Data Warehouse (VDW) consisting of harmonized data elements from both electronic health records (EHRs) and insurance claims data, which facilitated multisite research by allowing programs written at one site to be distributed and efficiently run at other health care systems. All data were extracted from the VDW. See the main paper by Weisner et al. for a detailed description of data sources and extraction methods.Citation17 Participants were adults (age ≥ 18) with at least 1 HEDIS-qualifying AOD use disorder diagnosis during the study period. This research was reviewed and approved by the Kaiser Permanente Northern California Institutional Review Board. This study met requirements for a waiver of informed consent.

Measures

Patient demographic characteristics

Measures included age, sex, and race/ethnicity.

Comorbidity

Comorbid psychiatric disorder diagnoses in the year prior to index identification date were based on International Classification of Diseases (ICD)-9 diagnosis codes. Presence of any psychiatric disorder diagnosis in the past year was dichotomously coded. Separate indicators for past-year psychiatric disorder were created for several diagnostic subcategories: depressive disorder (yes/no), anxiety disorder (yes/no), and psychotic disorder (yes/no), as well as an indicator for presence of a prior AOD use disorder diagnosis in the year prior to the index diagnosis but not within 60 days of the index diagnosis (yes/no).

Outcomes: Initiation and engagement

Treatment initiation was defined as a subsequent AOD treatment service (excluding emergency department [ED] visit or detoxification) within 14 days of the ED or outpatient claim/encounter index identification date. An inpatient index identification setting (excluding those for detoxification only, which account for 2% of inpatient index encounters) was considered to be initiation of treatment per HEDIS definition, whereas an ED or outpatient claim/encounter index identification diagnosis required a subsequent AOD service (not including detoxification or ED visits) within 14 days of the index diagnosis in order to be considered initiation. Engagement was defined as having 2 or more AOD-related services within 30 days following treatment initiation. Data elements required for calculating each of the treatment initiation and engagement variables included ICD-9 diagnosis codes (alcohol, opioid, barbiturate, cocaine, cannabis, amphetamine, hallucinogen, and unspecified), department, and dates of service. Initiation and engagement rates were calculated only for adult patients who had a “new” index diagnosis (as defined by having no AOD use disorder diagnoses in the 60 days before the index diagnosis) associated with an AOD abuse or dependence diagnosis between October 1, 2014, and August 15, 2015,Citation18 and were continuously enrolled in the health care system 2 months prior to through 44 days following the index date. Index diagnoses included diagnoses given at an ED, outpatient claim/encounter, or inpatient discharge encounter. Type of AOD use disorder diagnosis and care setting for the index diagnosis were identified for each patient.

Analytic plan

Descriptive analyses examined individual characteristics (e.g., age, sex, race/ethnicity), prior psychiatric disorder diagnoses (any psychiatric disorder, as well as specific subcategories of anxiety disorders, depressive disorders, psychotic disorders), and prior AOD use disorder diagnoses among patients with an AOD index diagnosis (N = 86,565). Bivariate comparisons examined characteristics of patients who initiated AOD treatment among those with and without a comorbid psychiatric disorder in the year prior to their index diagnosis. Then, among those patients who initiated AOD treatment, bivariate comparisons of characteristics of patients who engaged in AOD treatment were examined for those with and without a comorbid psychiatric disorder diagnosis in the year prior to index. Chi-square and t tests were used to examine differences between groups with regard to initiation and engagement.

Generalized linear models with a logit link, clustered on health care system with random intercept effect, were used to investigate the relationship between any psychiatric disorder diagnosis and AOD treatment initiation and engagement, and between diagnostic subcategories (anxiety disorders, depressive disorders, psychotic disorders, prior AOD use disorders) and AOD treatment initiation and engagement. Univariate models investigated the effect of each psychiatric disorder diagnosis on AOD IET. Multivariate models controlling for other covariates including age, sex, and race/ethnicity were also examined (Model 1 in ). Specific diagnostic subcategories of prior psychiatric disorders were then added to the final multivariate models controlling for covariates (Model 2 in ). Given previous research suggesting that factors affecting AOD treatment may differ for women and for men,Citation9–13 gender differences in AOD treatment initiation and engagement were examined in sensitivity analyses. All analyses were performed using SAS 9.4 (SAS Institute, Cary, NC).

Results

Patient characteristics

In this sample of 86,565 individuals with a new AOD use disorder diagnosis, the majority of patients (n = 57,335; 66.2%) had a comorbid psychiatric disorder diagnosis in the year prior to their index AOD diagnosis, including 41.7% (n = 36,079) who had a prior AOD use disorder diagnosis more than 60 days before the AOD index diagnosis, 27.4% (n = 23,705) with an anxiety disorder, 30.4% (n = 26,293) with a depressive disorder, and 11.4% (n = 9,879) with a psychotic disorder. Among patients with a comorbid psychiatric disorder, 34.9% (n = 19,998) initiated AOD treatment (see ), and of those who initiated treatment, 10.3% (n = 2,060) engaged in treatment (see ). Most patients with a comorbid psychiatric disorder initiated treatment through inpatient settings (n = 14,367; 71.8%), whereas most patients who engaged in treatment received the index diagnosis in an outpatient setting (n = 1,144; 55.5%).

Table 1. Initiation: Patient characteristics stratified by prior psychiatric disorders (N = 86,565).

Table 2. Engagement: Patient characteristics stratified by prior psychiatric disorders for those who initiated AOD treatment (n = 24,188).

Although men constituted a larger proportion of patients with an index AOD diagnosis (60.4% men vs. 39.6% women), women were more likely to have a comorbid psychiatric disorder (74.9% vs. 60.6%; P < .0001). Among patients who had a comorbid psychiatric disorder, a higher proportion of men initiated AOD treatment compared with women (P < .0001); however, there was no difference between men and women regarding engagement (P = .6416).

Multivariate analyses

Controlling for demographic characteristics (age, sex, and race/ethnicity), logistic regression analyses revealed that patients with a comorbid psychiatric disorder were more likely to initiate AOD treatment compared with those without a comorbid psychiatric disorder (odds ratio [OR] = 3.20, 95% confidence interval [CI] = 3.08, 3.32), but they were less likely to engage in AOD treatment (OR = 0.56, 95% CI = 0.51, 0.61). When adjusting for all psychiatric disorder diagnoses a year prior to AOD index diagnosis, patients with comorbid depressive (OR = 1.12, 95% CI = 1.07, 1.16), psychotic (OR = 1.40, 95% CI = 1.34, 1.47), or prior AOD use disorders (OR = 3.66, 95% CI = 3.54, 3.79) had higher odds of initiation compared with those without the respective disorders. Patients with comorbid anxiety (OR = 1.21, 95% CI = 1.10, 1.33) or depressive disorders (OR = 1.20, 95% CI = 1.09, 1.32) were more likely to engage in AOD treatment. Presence of a prior AOD use disorder diagnosis was associated with increased odds of initiating AOD treatment (OR = 3.66, 95% CI = 3.54, 3.79) but decreased odds of engaging in treatment (OR = 0.44, 95% CI = 0.40, 0.48). See .

Table 3. Univariate and multivariate logistic regression analyses for risk of diagnosis of psychiatric disorder a year prior to AOD index associated with AOD treatment initiation and engagement.

Discussion

The present study examined HEDIS AOD use disorder treatment initiation and engagement among those with and without a comorbid psychiatric disorder, among patients receiving care in 7 large health care systems in the United States. We expected that patients with a comorbid psychiatric disorder in the year prior to receiving an AOD index diagnosis would be more likely to both initiate and engage in AOD treatment compared with those without comorbid psychiatric disorders. Those with a comorbid psychiatric disorder were indeed more likely to initiate treatment, but rates of engagement did not differ compared with those without a comorbid psychiatric disorder. When we examined specific categories of psychiatric disorders, those with anxiety disorders were no more likely to initiate treatment compared with patients with other comorbid psychiatric disorders or those without comorbid psychiatric disorders, but they were more likely to engage in treatment once they initiated. Patients with comorbid depressive disorders were somewhat more likely to initiate and engage. Those with psychotic disorders were more likely to initiate treatment but less likely to engage. In particular, patients who had previously been diagnosed with an AOD use disorder prior to the index diagnosis were most likely to initiate treatment but least likely to engage in treatment. Overall, these findings suggest that patients with comorbid psychiatric disorders are more likely to initiate AOD treatment but may encounter other barriers to engaging in treatment, and engagement may be particularly challenging for those with multiple AOD use disorders. Therefore, patients with certain comorbid conditions may require tailored efforts to support initiation and engagement in AOD treatment.

In the present study, most patients with comorbid psychiatric disorders received their AOD index diagnosis through inpatient settings; however, most patients who went on to engage in AOD treatment received their index diagnosis in an outpatient setting. These findings have important implications for how health care systems identify and support patients in need of treatment for both psychiatric and AOD use disorders. Of note, identification and proper diagnosis of comorbid psychiatric and AOD use disorders can be complex due to symptom overlap and more acute issues such as intoxication and withdrawal. As a result, assessment and accurate diagnosis may take more time than may be available during a single ED or outpatient visit.

Previous research has demonstrated that patients with psychiatric and AOD use disorders often seek treatment in mental health settings rather than specialty AOD care settings.Citation3 Patients with comorbid psychiatric disorders may have established relationships with mental health providers treating their psychiatric conditions, thus enhancing the likelihood they would be interested in initiating AOD treatment, or perhaps facilitating referrals for specialty AOD care if needed. Ideally, treatment for comorbid psychiatric and AOD use disorders should be considered together during a treatment plan and addressed concurrently in a treatment program for dual diagnosis or co-occurring disorders, given the large number of AOD patients also presenting with a comorbid psychiatric condition and/or multiple AOD use disorders. Unfortunately, providers in mental health settings often do not effectively identify AOD problems nor recommend that patients reduce AOD use or initiate specialty AOD care.Citation19 Consequently, although having a comorbid psychiatric disorder may motivate patients to seek care, AOD use disorders may still be under-identified in settings serving patients with mental health problems. Further, among patients without an established mental health provider, such as the subset of those identified as having an AOD use disorder in an inpatient setting, our findings may reflect the health care system’s difficulty engaging patients with comorbid psychiatric and AOD use disorders in AOD treatment.

Individuals with comorbid psychiatric and AOD use disorders have more health care needsCitation20 and therefore may be more likely to make health care visits compared with individuals with AOD disorders only. Integrated AOD screening and treatment can help to identify patients in need of AOD treatment and enhance referrals to specialty AOD care.Citation21 Our findings underscore the importance of regular screening for both psychiatric and AOD use disorders in outpatient settings and providing immediate brief intervention, such as screening, brief intervention, and referral to treatment (SBIRT), which can improve access to specialty AOD care.Citation22

Importantly, although identification of a comorbid psychiatric disorder may increase the chances that an individual will initiate AOD treatment, rates of initiation and engagement in AOD treatment remain low overall. Nonetheless, special focus may be needed to enhance initiation and engagement in AOD treatment, especially for individuals without a comorbid psychiatric disorder, given the lower treatment uptake among this group.

Some prior studies have found gender differences in AOD treatment initiation and engagement,Citation9–13 whereas others have not found such differences.Citation23 We found that among patients with comorbid psychiatric disorders, men were more likely to initiate AOD treatment, but there were no gender differences in AOD treatment engagement. As others have noted, the relationship between AOD treatment initiation and engagement and gender is likely complex.Citation23 Future research should consider structural and other barriers related to accessing AOD treatment, including parsing out the multifaceted issues related to AOD treatment access for men and women, and how health care systems can better address these issues to support patients with comorbid psychiatric and AOD use disorders who could benefit from treatment.

Limitations

Data used in the present study are from EHR systems and reflect only diagnoses and encounter events coded by providers. As such, it is possible that some patients were misdiagnosed due to complexities in distinguishing between substance-induced disorders and idiopathic psychiatric disorders, for example. All AOD use disorders were grouped into a single category; however, it is possible that specific AOD use disorders may be associated with a unique pattern of comorbid disorders and treatment initiation and engagement. A limited number of subcategories of psychiatric diagnoses were available to examine separately from the overall category of any psychiatric disorder; therefore, the relative contributions of other diagnoses, such as personality disorders, were not examined. Although this reflects real-world practice, our data may not fully represent all patients with comorbid psychiatric and AOD use disorders receiving care within these 7 health care systems. In addition, some patients may have chosen to seek care outside of health care systems examined in the study (e.g., self-help groups or care at outside facilities); our data would not reflect such visits. Further, each health care system is organized differently with a diverse set of resources and providers, which can therefore lead to variations in EHR coding across health care systems, although our investigators across health care systems attempted to address this.

Future directions

Future investigations are needed to better understand system- and patient-level factors impacting AOD treatment initiation and engagement for patients with comorbid psychiatric and AOD use disorders.

Conclusion

Our study examined AOD treatment initiation and engagement following an AOD index diagnosis among patients with and without comorbid psychiatric disorders who were receiving care through 7 health care systems. Findings suggested that identification of a comorbid psychiatric disorder may increase initiation of AOD treatment but may not impact engagement in AOD treatment. Innovative efforts are needed to enhance AOD treatment initiation, especially for individuals without diagnosed psychiatric conditions, and engagement more generally.

Acknowledgments

We thank Andrea Altschuler, PhD, at Kaiser Permanente Northern California for her contributions.

Additional information

Funding

This study was supported by a grant from the National Institute of Drug Abuse (NIDA) (5UG1DA040314-03). The content is solely the responsibility of the authors and does not necessarily represent the official views of NIDA. The NIDA Clinical Trials Network (CTN) Research Development Committee reviewed the study protocol, and the NIDA CTN publications committee reviewed and approved the manuscript for publication. The funding organization had no role in the collection, management, analysis, and interpretation of the data or decision to submit the manuscript for publication.

Notes on contributors

Amy M. Loree

A.M.L. contributed to the conception of the analyses and wrote the manuscript. H.Y. conceived of and conducted the analysis. D.D.S. critically revised the manuscript. A.H.K.-S. coordinated data collection across sites, oversaw analysis, and drafted portions of the Methods section. B.Y.J., I.V.H., C.I.C., G.T.L., and R.C.H. contributed data and critically revised the manuscript. I.A.B. contributed data. C.W. oversaw research conception and design. B.K.A. contributed data, contributed to the conception of the analyses, and critically revised the manuscript.

Hsueh-Han Yeh

A.M.L. contributed to the conception of the analyses and wrote the manuscript. H.Y. conceived of and conducted the analysis. D.D.S. critically revised the manuscript. A.H.K.-S. coordinated data collection across sites, oversaw analysis, and drafted portions of the Methods section. B.Y.J., I.V.H., C.I.C., G.T.L., and R.C.H. contributed data and critically revised the manuscript. I.A.B. contributed data. C.W. oversaw research conception and design. B.K.A. contributed data, contributed to the conception of the analyses, and critically revised the manuscript.

Derek D. Satre

A.M.L. contributed to the conception of the analyses and wrote the manuscript. H.Y. conceived of and conducted the analysis. D.D.S. critically revised the manuscript. A.H.K.-S. coordinated data collection across sites, oversaw analysis, and drafted portions of the Methods section. B.Y.J., I.V.H., C.I.C., G.T.L., and R.C.H. contributed data and critically revised the manuscript. I.A.B. contributed data. C.W. oversaw research conception and design. B.K.A. contributed data, contributed to the conception of the analyses, and critically revised the manuscript.

Andrea H. Kline-Simon

A.M.L. contributed to the conception of the analyses and wrote the manuscript. H.Y. conceived of and conducted the analysis. D.D.S. critically revised the manuscript. A.H.K.-S. coordinated data collection across sites, oversaw analysis, and drafted portions of the Methods section. B.Y.J., I.V.H., C.I.C., G.T.L., and R.C.H. contributed data and critically revised the manuscript. I.A.B. contributed data. C.W. oversaw research conception and design. B.K.A. contributed data, contributed to the conception of the analyses, and critically revised the manuscript.

Bobbi Jo H. Yarborough

A.M.L. contributed to the conception of the analyses and wrote the manuscript. H.Y. conceived of and conducted the analysis. D.D.S. critically revised the manuscript. A.H.K.-S. coordinated data collection across sites, oversaw analysis, and drafted portions of the Methods section. B.Y.J., I.V.H., C.I.C., G.T.L., and R.C.H. contributed data and critically revised the manuscript. I.A.B. contributed data. C.W. oversaw research conception and design. B.K.A. contributed data, contributed to the conception of the analyses, and critically revised the manuscript.

Irina V. Haller

A.M.L. contributed to the conception of the analyses and wrote the manuscript. H.Y. conceived of and conducted the analysis. D.D.S. critically revised the manuscript. A.H.K.-S. coordinated data collection across sites, oversaw analysis, and drafted portions of the Methods section. B.Y.J., I.V.H., C.I.C., G.T.L., and R.C.H. contributed data and critically revised the manuscript. I.A.B. contributed data. C.W. oversaw research conception and design. B.K.A. contributed data, contributed to the conception of the analyses, and critically revised the manuscript.

Cynthia I. Campbell

A.M.L. contributed to the conception of the analyses and wrote the manuscript. H.Y. conceived of and conducted the analysis. D.D.S. critically revised the manuscript. A.H.K.-S. coordinated data collection across sites, oversaw analysis, and drafted portions of the Methods section. B.Y.J., I.V.H., C.I.C., G.T.L., and R.C.H. contributed data and critically revised the manuscript. I.A.B. contributed data. C.W. oversaw research conception and design. B.K.A. contributed data, contributed to the conception of the analyses, and critically revised the manuscript.

Gwen T. Lapham

A.M.L. contributed to the conception of the analyses and wrote the manuscript. H.Y. conceived of and conducted the analysis. D.D.S. critically revised the manuscript. A.H.K.-S. coordinated data collection across sites, oversaw analysis, and drafted portions of the Methods section. B.Y.J., I.V.H., C.I.C., G.T.L., and R.C.H. contributed data and critically revised the manuscript. I.A.B. contributed data. C.W. oversaw research conception and design. B.K.A. contributed data, contributed to the conception of the analyses, and critically revised the manuscript.

Rulin C. Hechter

A.M.L. contributed to the conception of the analyses and wrote the manuscript. H.Y. conceived of and conducted the analysis. D.D.S. critically revised the manuscript. A.H.K.-S. coordinated data collection across sites, oversaw analysis, and drafted portions of the Methods section. B.Y.J., I.V.H., C.I.C., G.T.L., and R.C.H. contributed data and critically revised the manuscript. I.A.B. contributed data. C.W. oversaw research conception and design. B.K.A. contributed data, contributed to the conception of the analyses, and critically revised the manuscript.

Ingrid A. Binswanger

A.M.L. contributed to the conception of the analyses and wrote the manuscript. H.Y. conceived of and conducted the analysis. D.D.S. critically revised the manuscript. A.H.K.-S. coordinated data collection across sites, oversaw analysis, and drafted portions of the Methods section. B.Y.J., I.V.H., C.I.C., G.T.L., and R.C.H. contributed data and critically revised the manuscript. I.A.B. contributed data. C.W. oversaw research conception and design. B.K.A. contributed data, contributed to the conception of the analyses, and critically revised the manuscript.

Constance Weisner

A.M.L. contributed to the conception of the analyses and wrote the manuscript. H.Y. conceived of and conducted the analysis. D.D.S. critically revised the manuscript. A.H.K.-S. coordinated data collection across sites, oversaw analysis, and drafted portions of the Methods section. B.Y.J., I.V.H., C.I.C., G.T.L., and R.C.H. contributed data and critically revised the manuscript. I.A.B. contributed data. C.W. oversaw research conception and design. B.K.A. contributed data, contributed to the conception of the analyses, and critically revised the manuscript.

Brian K. Ahmedani

A.M.L. contributed to the conception of the analyses and wrote the manuscript. H.Y. conceived of and conducted the analysis. D.D.S. critically revised the manuscript. A.H.K.-S. coordinated data collection across sites, oversaw analysis, and drafted portions of the Methods section. B.Y.J., I.V.H., C.I.C., G.T.L., and R.C.H. contributed data and critically revised the manuscript. I.A.B. contributed data. C.W. oversaw research conception and design. B.K.A. contributed data, contributed to the conception of the analyses, and critically revised the manuscript.

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