Abstract
BACKGROUND:
Foster youth have higher rates of psychotropic medication use and concurrent multiclass psychotropic polypharmacy compared with nonfoster youth. However, less is known about the extent of multiclass psychotropic polypharmacy after adjusting for patient factors associated with psychotropic medication use
OBJECTIVES:
To (a) compare psychotropic medication use and psychotherapy use by youth in foster care to those not in foster care in the Oklahoma Medicaid population across various sociodemographic and clinical factors, and (b) determine if patient-related characteristics are associated with high levels of concurrent multiclass psychotropic polypharmacy.
METHODS:
This cross-sectional, retrospective analysis was conducted using paid prescription, outpatient, and inpatient Oklahoma Medicaid administrative claims from calendar year 2016. Foster youth and adolescents aged 20 years or younger were identified (n = 9,325) and compared with the general Oklahoma Medicaid population of the same age (n = 639,868). Descriptive statistics highlight baseline demographic and clinical differences between the 2 groups. Multivariable logistic regression was used to determine if covariates were associated with concurrent multiclass psychotropic polypharmacy. A subgroup analysis of foster youth taking at least 1 psychotropic medication was also performed to determine factors associated with the highest level of concurrent multiclass psychotropic polypharmacy.
RESULTS:
Foster care was associated with higher odds of concurrent multiclass psychotropic polypharmacy regardless of presence of psychotherapy. Among the subgroup of foster youth taking at least 1 psychotropic medication, attention deficit hyperactivity disorder medications were the most commonly prescribed medication class, followed by antidepressants and anxiolytics when use was not chronic. However, at the highest level of chronic multiclass psychotropic polypharmacy (4-5 chronic concurrent medications), antipsychotics rose to the top, and anxiolytics were the least likely to be prescribed. Overall, the foster care population had the highest proportion of individuals with concurrent multiclass psychotropic polypharmacy (9.2% vs. 1.9%, P < 0.0001). The highest level of chronic multiclass psychotropic polypharmacy was more likely to occur in males (OR = 1.66, 95% CI = 1.40-1.96) and patients living in group homes (OR = 4.13, 95% CI = 2.02-8.44) or foster homes (OR = 1.66, 95% CI = 1.25-2.19). Being overweight or obese was associated with an 83% higher odds of being at the highest level of concurrent multiclass psychotropic polypharmacy (95% CI = 1.27-2.64).
CONCLUSIONS:
Despite higher psychotherapy use, high rates of psychotropic medication use and concurrent multiclass psychotropic polypharmacy in foster youth remain a concern for policymakers. Patterns observed at different levels of concurrent multiclass psychotropic polypharmacy may be key to identifying youth who require additional monitoring. Future research exploring factors associated with higher levels of psychotropic concurrent multiclass psychotropic polypharmacy in foster youth can lead to actionable interventions and important policy changes.
What is already known about this subject
Foster youth are more likely to be prescribed psychotropic medications in comparison with other youth.
Foster youth have higher rates of psychotropic polypharmacy.
Youth in foster care have higher utilization rates of health services.
What this study adds
Increase in age, being male, increasing Deyo Charlson Comorbidity Index score, being overweight or obese, and presence of hyperlipidemia were associated with higher odds of concurrent multiclass psychotropic polypharmacy among youth.
Although foster youth receiving psychotherapy have lower odds of concurrent multiclass psychotropic polypharmacy than those not receiving psychotherapy, foster youth are still at higher odds of taking psychotropic medications compared with their nonfoster counterparts regardless of the presence of psychotherapy.
ADHD medications are most commonly prescribed when youth are taking 3 or fewer medications, and antipsychotic medications are most commonly prescribed among youth taking 4-5 medications.
Concern about psychotropic medication use in foster youth has been well documented in the literature. Studies consistently show that foster youth use more psychotropic medication compared with other youth, including other youth on Medicaid.1-3 Foster youth also have higher rates of taking multiple psychotropic medications either within the same class or between multiple different medication classes.4-9
Foster youth are a vulnerable population at increased risk for adverse childhood experiences compared with other children, even after controlling for income and family structure.10 Foster youth also have twice the prevalence of mental health disorders compared with nonfoster youth receiving Supplemental Security Income.11 In addition, these youth use mental health services at higher rates than other children.12 However, despite the prevalence of mental health issues that make this population more susceptible to psychotropic medication use and known concerns of psychotropic overprescribing among foster youth, use of these medications still occurs at high rates.13,14
Policymakers have taken notice of the high levels of psychotropic medication use and polypharmacy among foster youth. The American Academy of Child and Adolescent Psychiatry published guidelines to promote safe use of psychotropic medications in children and adolescents.15 By 2010, 26 states had guidelines for psychotropic medication use in foster children, and 13 more had guidelines in development.16 The increase in antipsychotic prescribing for children and adolescents over recent decades has also prompted the National Committee for Quality Assurance’s Healthcare Effectiveness Data and Information Set (HEDIS) to include the use of multiple concurrent antipsychotics by children and adolescents as one of their outcome measures.17 It included this measure because youth prescribed antipsychotics are at risk for weight gain, extrapyramidal side effects, hyperprolactinemia, and metabolic effects, so this measure can highlight potentially unsafe use of antipsychotic medications.18 Although these policy initiatives show promise in curbing observed upward trends in psychotropic medication use and polypharmacy among children and adolescents,14 recent studies are still finding high levels of psychotropic medication use and polypharmacy among foster youth.8,9
There remains an opportunity to better understand concurrent multiclass psychotropic polypharmacy (use of at least 2 classes of psychotropic medications concurrently for at least 90 consecutive days) alongside psychotherapy and to better understand prescription patterns at various levels of psychotropic polypharmacy in this population. The primary objective of this study was to describe psychotropic medication and psychotherapy use by youth in foster care in the Oklahoma Medicaid population compared with those not in foster care. Secondary objectives were to describe the prevalence of each drug class across different levels of concurrent multiclass psychotropic polypharmacy and identify patient-related characteristics associated with the highest level of concurrent multiclass psychotropic polypharmacy.
Methods
Data Source
Data for this research used computerized, individual-level prescription, outpatient, and inpatient Oklahoma Medicaid claims and eligibility data from the Oklahoma Health Care Authority (OHCA), along with foster care eligibility data from the Oklahoma Department of Human Services (ODHS). Pharmacy Management Consultants (PMC), a department of the University of Oklahoma College of Pharmacy, maintains administrative claims data for OHCA in a secure environment. Use of the data was part of an agreement between PMC, OHCA, and ODHS. Data were extracted and deidentified for research purposes. The institutional review boards at the University of Oklahoma Health Sciences Center and ODHS approved this study.
Study Design
Stakeholders from PMC, OHCA, and ODHS initiated this research with guidance from local practitioners and individuals involved in caring for children and adolescents in foster care. This cross-sectional, retrospective analysis of paid administrative claims was part of a larger mixed-methods project assessing the psychotropic medication use process in Oklahoma foster youth. The review period was January 1, 2016-December 31, 2016. Oklahoma Medicaid (MOK) youth were included in the review if they were eligible for MOK at any time during the review period and were aged 0-20 years (defined as a child by OHCA). Any person designated as foster care, but with unconfirmed MOK eligibility was excluded. A subgroup analysis was performed on foster youth with any use of attention deficit hyperactivity disorder (ADHD), antidepressant, antipsychotic, mood stabilizer, and/or anxiolytic medications. This subgroup was analyzed across 4 levels: nonchronic use (lowest), chronic single-class use, 2-3 classes, or 4-5 classes (highest).
Outcomes
The outcomes for this research were based on metrics adapted from the Medicaid/Mental Health Network for Evidence Based Treatment (MEDNET) collaboration.19 The metrics were designed to determine various drug or service patterns of use within the Medicaid population. The primary outcome was concurrent multiclass polypharmacy (defined as concurrent use of at least 2 different classes of medications for 90 or more consecutive days). For the subgroup analysis, the outcome of concurrent multiclass polypharmacy was divided into nonchronic use (lowest), chronic single-class use, 2-3 concurrent classes, or 4-5 concurrent classes (highest).
The classes of psychotropic medications selected for review were identified by a Generic Product Identifier20 and included ADHD, anti-anxiety, depression, first- and second-generation antipsychotics, and mood stabilizers. ADHD medications included amphetamines salts, clonidine, guanfacine, atomoxetine, methylphenidate, and dexmethylphenidate. Anxiolytic medications included benzodiazepines, hydroxyzine, and buspirone. Antidepressant medications included selective serotonin reuptake inhibitors, tricyclic antidepressants, serotonin and norepinephrine reuptake inhibitors, mirtazapine, doxepin, trazodone, and bupropion. As stated, antipsychotics included all first- and second-generation products. Mood stabilizers included valproic acid, carbamazepine, lamotrigine, oxcarbazepine, and lithium.
Covariates
Covariates were determined using the Andersen framework for health care utilization.21 This framework is used to understand health care utilization at several levels of determinants of health. The 3 levels assessed in this study were predisposing factors, enabling factors, and need factors.
Predisposing factors included were age (calculated as age on the last day of the review period); sex (male or female); self-reported race; and length of MOK eligibility during the review year (in months). Subjects who reported more than 1 race were combined into a single classification for multiple races. Marital status and occupation were not assessed given the age of the population. Education level was not included in the data available for the study.
Core-based statistical area (CBSA) designation served as an enabling factor because disparities in access to health care exist between rural and urban areas.22 Counties are classified as rural, micropolitan, or metropolitan based on their population size as of the 2010 census.23 The CBSA designation covariate was split into rural versus micropolitan and metropolitan.
Clinical characteristics and psychotherapy served as need factors. Those included were presence of a mental health-related diagnosis, psychotherapy, Deyo Charlson Comorbidity Index (DCCI) score,24 having overweight or obese status, hyperlipidemia, opioid dependence, and nonopioid substance abuse. International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) diagnosis codes within the claims data served as identifiers for presence of hyperlipidemia (E78.5). The variable for body mass index was recoded as a dummy variable, where overweight or obese status = 1 based on the presence of ICD-10-CM diagnosis codes for overweight or obesity (E66.x). DCCI score is derived from an algorithm of diagnosis codes and a higher comorbidity index correlates to more comorbidities.25 The mental health services codes used to define psychotherapy were determined by the collaborative research team (available from the authors upon request).
Statistical Analysis
Descriptive statistics were calculated using chi-square, Fisher’s exact, or Student’s t-tests (where appropriate) to assess baseline demographic and clinical differences between foster youth and Medicaid youth not in foster care. Multivariable logistic regression was used to determine if the collected covariates were factors associated with concurrent multiclass psychotropic polypharmacy. Ordered logistic regression was used to analyze the subgroup of the foster care population that had received at least 1 claim for a psychotropic medication to determine whether covariates were associated with having a higher level of polypharmacy. All analyses were performed using SAS version 9.4 (SAS Institute, Cary, NC).
Results
From January 1, 2016, to December 31, 2016, a total of 649,193 Oklahoma Medicaid youth were identified as eligible for this study. Of those, 9,481 were identified as in foster care. After applying exclusions, 639,868 nonfoster and 9,325 foster care members remained (Figure 1). Table 1 highlights the demographics of these 2 groups. Compared with the nonfoster youth, the foster care population was younger (6.4 years vs. 8.7 years, P < 0.001), with most youth aged less than 4 years. A larger proportion of foster care youth self-identified with multiple races compared with the general population (22.8% vs. 15.9%, P < 0.001). The foster care population maintained a longer average period of eligibility (10.9 months vs. 9.9 months, P < 0.001). Based on utilization data, foster youth had a higher proportion of overall prescription medication use than the general population (77.9% vs. 62.4%, P < 0.001), as well as higher use of psychotropic medications (22.4% vs. 10.6%, P < 0.001). Although medical claims were high in both populations, nearly all foster youth had at least 1 medical claim (97.7% vs. 71.6%, P < 0.001). While the presence of chronic conditions was low for both populations, the foster care population had a higher DCCI score (0.10 vs. 0.07, P < 0.001). However, this difference may not be clinically significant. There were no significant differences in occurrence of opioid dependence, occurrence of nonopioid substance abuse, presence of hyperlipidemia, or being overweight/obese between the 2 groups.
TABLE 1.
Nonfostera (n = 639,868) | Fostera (n = 9,325) | P Value | |
---|---|---|---|
Age, mean (SD) | 8.73 (5.72) | 6.41 (5.00) | < 0.001 |
Age group, years | |||
0-4 | 29.2 (186,691) | 43.9 (4,090) | < 0.001 |
5-12 | 41.6 (266,011) | 40.8 (3,802) | |
13-20 | 29.3 (187,166) | 15.4 (1,433) | |
Sex (male) | 50.5 (323,229) | 52.1 (4,857) | 0.003 |
Race | |||
White | 59.6 (381,237) | 55.2 (5,150) | < 0.001 |
Black | 11.2 (71,532) | 12.0 (1,122) | |
Asian | 1.5 (9,542) | 0.2 (15) | |
American Indian or Alaskan Native | 11.5 (73,475) | 9.7 (904) | |
Native Hawaiian or Pacific Islander | 0.4 (2,420) | 0.1b | |
Mixed | 15.9 (101,592) | 22.8 (2,124) | |
Unknown | 0.1 (70) | 0.0b | |
CBSA designation | |||
Rural | 16.3 (104,546) | 16.2 (1,508) | 0.333 |
Metro or micro | 82.4 (527,001) | 83.8 (7,813) | |
Unknown | 1.3 (8,321) | 0.04b | |
DCCI score, mean (SD) | 0.07 (0.29) | 0.10 (0.34) | < 0.001 |
Overweight/obese | 2.0 (12,641) | 2.2 (203) | 0.167 |
Hyperlipidemia | 0.4 (2,284) | 0.3 (26) | 0.208 |
Mean months eligible, mean (SD) | 9.89 (3.4) | 10.88 (2.5) | < 0.001 |
Receiving any prescription medication | 62.4 (399,206) | 77.9 (7,264) | < 0.001 |
Received any psychotropic medication | 10.6 (67,886) | 22.4 (2,092) | < 0.001 |
ADHD | 6.6 (42,317) | 16.9 (1,576) | < 0.001 |
Antipsychotics | 1.7 (10,724) | 8.7 (808) | |
Depression | 4.2 (26,998) | 11.9 (1,113) | |
Mood | 1.1 (6,829) | 4.8 (451) | |
Anxiolytics | 2.6 (16,502) | 4.64 (433) | |
Single-class polypharmacyc | |||
ADHD | 1.4 (8,704) | 5.3 (492) | < 0.001 |
Antipsychotics | 0.1 (297) | 0.3 (32) | |
Depression | 0.3 (2,198) | 1.9 (174) | |
Mood | 0.0 (208) | 0.2 (20) | |
Anxiolytics | 0.0 (89) | 0.0b | |
Concurrent multiclass psychotropic polypharmacyd | 1.9 (12,394) | 9.2 (859) | < 0.001 |
Two classes | 1.3 (8,010) | 4.5 (418) | < 0.001 |
Three classes | 0.5 (3,366) | 3.3 (310) | |
Four classes | 0.1 (897) | 1.3 (121) | |
Five or more classes | 0.0 (121) | 0.1 (10) | |
Presence of psychotherapy | 4.0 (25,498) | 22.4 (2,086) | < 0.001 |
aAll values are % (n) unless otherwise indicated.
bCell counts with less than 10 individuals were suppressed to protect patient privacy.
cOne or more of the same class of medications on the same day for 90 consecutive days or longer.
dOne or more classes of mental health medications on the same day for 90 consecutive days or longer.
ADHD = attention deficit hyperactivity disorder; CBSA = core-based statistical area; DCCI = Deyo Charlson Comorbidity Index; SD = standard deviation.
While ADHD medications were the most commonly prescribed class of psychotropic medication regardless of foster care status, more foster youth received a medication from this class compared with youth not in foster care (16.9% vs. 6.6%, P < 0.001). Similarly, of youth meeting criteria for single-class polypharmacy, ADHD medications were the most frequently prescribed drug class in both populations, but more foster youth received these medications than youth not in foster care (5.3% vs. 1.4%, P < 0.001). Polypharmacy was also significantly higher for foster youth in each of the medication classes except anxiolytics (P < 0.001 for antipsychotics, depression, and mood classes). In addition, overall presence of concurrent multiclass psychotropic polypharmacy was higher in foster youth compared with the general population (9.2% vs. 1.9%, P < 0.001). Psychotherapy in foster youth was higher than the general population (22.4% vs. 4.0%, P < 0.001). Furthermore, the percentage of foster youth using each type of service was also higher than observed in the nonfoster group (P < 0.001 for all), with psychotherapy being substantially higher in foster youth (22.4% vs. 4.0%).
Several patient factors were associated with increased odds of having concurrent multiclass psychotropic polypharmacy after adjusting for covariates (Table 2). Each increase in 1 year of age was associated with a 14.5% higher odds of concurrent multiclass psychotropic polypharmacy (odds ratio [OR] = 1.15, 95% confidence interval [CI] = 1.14-1.15) as was being male (OR = 1.89, 95% CI = 1.82-1.96). Being any race other than white or living in a rural location (OR = 0.89, 95% CI = 0.84-0.93) was associated with lower odds of psychotropic polypharmacy. The clinical characteristics of being overweight or obese (OR = 1.50, 95% CI = 1.37-1.64), having hyperlipidemia (OR = 1.73, 95% CI = 1.45-2.07), and each increase in 1 point in DCCI score (OR = 1.42, 95% CI = 1.36-1.48) were associated with increased odds of psychotropic polypharmacy.
TABLE 2.
Effect | Odds Ratio | 95% CI | |
---|---|---|---|
Age, years | 1.15a | 1.14 | 1.15 |
Male (reference = female) | 1.89a | 1.82 | 1.96 |
American Indian or Alaskan Native (reference = white) | 0.71a | 0.66 | 0.75 |
Asian (reference = white) | 0.19a | 0.13 | 0.27 |
Black (reference = white) | 0.56a | 0.52 | 0.59 |
Mixed (reference = white) | 0.84a | 0.79 | 0.90 |
Native Hawaiian or Pacific Island (reference = white) | 0.42a | 0.26 | 0.68 |
Rural (reference = urban) | 0.89a | 0.84 | 0.93 |
DCCI score, mean | 1.42a | 1.36 | 1.48 |
Presence of overweight/obesity | 1.50a | 1.37 | 1.64 |
Presence of hyperlipidemia | 1.73a | 1.45 | 2.07 |
Foster care vs. nonfoster care receiving no psychotherapy | 5.81a | 5.18 | 6.52 |
Foster care vs. nonfoster care receiving psychotherapy | 2.22a | 1.99 | 2.48 |
aStatistically significant at P < 0.05.
CI = confidence interval; DCCI = Deyo Charlson Comorbidity Index.
Given an interaction between foster care status and psychotherapy, individuals in foster care receiving no psychotherapy had higher odds of polypharmacy than individuals not in foster care receiving no psychotherapy (OR = 5.81, 95% CI = 5.18-6.52; Table 2). In addition, individuals in foster care receiving psychotherapy had higher odds of polypharmacy than those not in foster care receiving psychotherapy (OR = 2.22, 95% CI = 1.99-2.48).
Demographics of a subgroup analysis of foster youth taking any targeted psychotropic medication are highlighted in Table 3. Those in the highest level of multiclass use (4-5 chronic psychotropic medications) had a mean age of 13.1 years, whereas single class chronic use had the lowest mean age (9.3 years). No youth aged 4 years or younger were prescribed medications in the highest level (4-5 chronic psychotropic medications). The proportion of males and whites increased from the lowest to the highest level of use (53.7%-71.0% and 51.0%-65.7%). A higher proportion of those in the 4-5 chronic psychotropic medication classes subgroup were classified as being overweight/obese (12.2%, P < 0.001) and having hyperlipidemia (3.1%, P = 0.004) compared with those in the other levels of chronic psychotropic polypharmacy. ADHD was the most commonly prescribed medication class for those with nonchronic use to those taking 2-3 chronic psychotropic medications. However, antipsychotics were the most commonly prescribed medication class among those taking 4-5 concurrent psychotropic medications.
TABLE 3.
Nonchronic Psychotropic Medication Usea (n = 775) | Single-Class Chronic Psychotropic Medication Usea (n = 458) | 2-3 Chronic Psychotropic Medication Classesa (n = 728) | 4-5 Chronic Psychotropic Medication Classesa (n = 131) | P Value | |
---|---|---|---|---|---|
Age, mean (SD) | 10.15 (4.53) | 9.29 (3.58) | 11.74 (3.34) | 13.13 (2.89) | < 0.001 |
Age group, years | < 0.001 | ||||
0-4 | 11.4 (88) | 4.8 (22) | 0.3c | 0.0c | |
5-12 | 53.9 (418) | 74.0 (339) | 57.2 (416) | 35.9 (47) | |
13-20 | 34.7 (269) | 21.2 (97) | 42.6 (310) | 64.1 (84) | |
Sex (male) | 53.7 (416) | 62.2 (285) | 60.2 (438) | 71.0 (93) | 0.001 |
Race | 0.003 | ||||
White | 51.0 (395) | 51.8 (237) | 56.3 (410) | 65.7 (86) | |
Black | 12.4 (96) | 9.6 (44) | 12.8 (93) | 9.9 (18) | |
American Indian or Alaskan Native | 10.3 (80) | 8.5 (39) | 5.4 (39) | 4.6c | |
Mixed | 26.1 (202) | 29.5 (135) | 24.7 (180) | 19.9 (86) | |
Unknownb,c | 0.3c | 0.7c | 0.8c | 0.0c | |
Rural | 16.1 (125) | 14.2 (65) | 16.1 (117) | 10.7 (14) | 0.345 |
Mean months eligible, mean (SD) | 11.55 (1.51) | 11.88 (0.68) | 11.91 (0.64) | 11.98 (0.15) | < 0.001 |
Receiving psychotherapy | 36.5 (283) | 48.0 (220) | 61.4 (447) | 53.4 (70) | < 0.001 |
Residence status | < 0.001 | ||||
Own residence | 14.2 (110) | 49.7 (53) | 0.4 (62) | 35.7c | |
Foster home | 49.7 (385) | 50.2 (230) | 51.1 (372) | 45.8 (60) | |
Group home | 0.4c | 1.3c | 2.5 (18) | 3.8c | |
Other | 35.7 (277) | 36.9 (169) | 37.9 (276) | 45.0 (59) | |
Overweight/obese | 4.1 (32) | 2.4 (11) | 7.3 (53) | 12.2 (16) | < 0.001 |
Hyperlipidemia | 0.7c | 0.2c | 0.8c | 3.1c | 0.004 |
DCCI score, mean (SD) | 0.12 (0.37) | 0.13 (0.46) | 0.11 (0.34) | 0.11 (0.38) | 0.508 |
Medication utilization | |||||
ADHD | 57.7 (447) | 81.4 (373) | 86.1 (627) | 98.5 (129) | < 0.001 |
Antipsychotic | 17.3 (134) | 10.7 (49) | 68.0 (495) | 99.2 (130) | < 0.001 |
Antidepressant | 39.6 (307) | 26.0 (119) | 76.9 (560) | 97.0 (127) | < 0.001 |
Mood stabilizer | 12.0 (93) | 6.1 (28) | 30.4 (221) | 83.2 (109) | < 0.001 |
Anxiolytic | 24.0 (186) | 10.7 (49) | 19.2 (140) | 44.3 (58) | < 0.001 |
aAll values are % (n) unless otherwise indicated.
bThe 11 members of unknown race were excluded from the final regression model (Table 4).
cCell counts with less than 10 individuals were suppressed to protect patient privacy.
ADHD = attention deficit hyperactivity disorder; DCCI = Deyo Charlson Comorbidity Index; SD = standard deviation.
Controlling for independent variables, the odds of the highest level of multiclass chronic psychotropic polypharmacy (4-5 medication classes) compared with lower levels of polypharmacy was 2.1 times greater for those with psychotherapy than for those with no psychotherapy (95% CI = 1.80-2.49; Table 4). High-level chronic psychotropic use was also more likely in males (OR = 1.66, 95% CI = 1.40-1.96). Being overweight or obese was associated with an 83% higher odds of the highest level of concurrent multiclass psychotropic polypharmacy compared with those who were not overweight or obese (95% CI = 1.27-2.64). Compared with living in their own residence, living in a foster home, a group home, or other type of home were all associated with the highest level of concurrent multiclass psychotropic polypharmacy. High-level psychotropic use was not associated with presence of hyperlipidemia, an increased DCCI score, black race, mixed race, or rural location.
TABLE 4.
Effect | Odds Ratio | 95% CI | |
---|---|---|---|
Presence of psychotherapy (reference = none) | 2.12a | 1.80 | 2.49 |
Age, years | 1.11a | 1.09 | 1.13 |
Male (reference = female) | 1.66a | 1.40 | 1.96 |
American Indian or Alaskan Native (reference = white) | 0.58a | 0.42 | 0.79 |
Black (reference = white) | 0.79 | 0.61 | 1.02 |
Mixed (reference = white) | 0.84 | 0.69 | 1.01 |
Rural (reference = urban) | 1.00 | 0.79 | 1.25 |
Foster home (reference = own residence) | 1.66a | 1.25 | 2.19 |
Group home (reference = own residence) | 4.13a | 2.02 | 8.44 |
Other (reference = own residence) | 1.77a | 1.33 | 2.36 |
Overweight/obese (reference = not overweight or obese) | 1.83a | 1.27 | 2.64 |
Presence of hyperlipidemia (reference = none) | 2.52 | 0.99 | 6.40 |
DCCI, mean | 0.92 | 0.74 | 1.14 |
aStatistically significant at P < 0.05.
CI = confidence interval; DCCI = Deyo Charlson Comorbidity Index.
Discussion
Implications
This study compared psychotropic medication use and psychotherapy occurrence for foster care youth versus youth not in foster care in a state Medicaid population and observed differences in concurrent multiclass psychotropic polypharmacy among foster youth versus nonfoster youth, such as increase in age, being male, increase in DCCI score, being overweight or obese, and having hyperlipidemia. However, being any race other than white and living in a rural location were associated with lower odds of concurrent multiclass psychotropic polypharmacy. Oklahoma foster youth have higher proportions of psychotherapy than youth in the general Oklahoma Medicaid population, which is similar to findings by researchers examining Delaware’s Medicaid program.26 However, Oklahoma foster youth also have a higher proportion of psychotropic medication use and a higher odds of concurrent multiclass psychotropic polypharmacy compared with youth in the general Oklahoma Medicaid population regardless of psychotherapy. Therefore, opportunities remain to better understand factors involved in psychotropic medication prescribing for foster youth.
Adverse effects are a concern with long-term use of antipsychotic medications, especially in foster youth.27-29 Oklahoma foster youth had a slightly higher DCCI score, and after adjusting for other covariates, metabolic variables such as being overweight or obese and hyperlipidemia were associated with a higher odds of concurrent multiclass psychotropic polypharmacy in foster youth compared with nonfoster youth. Therefore, metabolic monitoring of youth taking psychotropic medications, as Oklahoma Medicaid policy requires,30 should continue. However, data in this study did not allow for examination of the extent of metabolic monitoring in this population.
Results of this study indicate that foster youth are still more likely to receive psychotropic medications than their nonfoster counterparts. Higher psychotropic medication use was observed in individuals in foster care compared with those not in foster care. Although psychotherapy plays a role in lessening the odds associated with psychotropic medications, foster youth are still at a higher odds of taking psychotropics compared with their nonfoster counterparts regardless of whether they are receiving psychotherapy.
The most common medication class to be present at up to 2-3 chronic psychotropic medication class level is ADHD. However, for those taking 4-5 medication classes, antipsychotics become the highest occuring medication. ADHD medications have previously been identified as the most common drug class at various levels of psychotropic polypharmacy among Medicaid youth.5,7,9,31 However, less is known about which medication is most commonly prescribed at various levels of polypharmacy within a cohort of only foster youth. Zito et al. (2008) reported a similar trend of ADHD being the most commonly prescribed medication class at lower levels of multiclass polypharmacy, with antipsychotic medications being most common at the highest level.32 Over 10 years later, in a different Medicaid population, our study found a similar pattern. Recently, Moran et al. (2019) found that approximately 1 in 660 adolescents are at risk of new-onset psychosis after receiving a prescription for an ADHD medication.33 Prescription of antipsychotic medications after initiation of ADHD medications may be a potential point to identify foster youth who may require monitoring or therapeutic interventions.
Another key finding in this study was the observation that no youth aged 4 years and younger had been prescribed medications at the highest level of concurrent multiclass psychotropic polypharmacy. Since 2010, the Oklahoma Medicaid program has used a pediatric psychiatric consultation service and prior authorization program for antipsychotics for youth aged 4 years and younger.34 This program requires all antipsychotic prescriptions for youth in this age range to be reviewed by a pediatric psychiatrist before approval. The psychiatrist service is also available for prescribers to consult with regarding any treatment regimens for pediatric Medicaid patients. This program may be an important reason for the low rate of polypharmacy in this population. It is also important to note that foster care youth had a higher percentage of children aged 4 years and under compared with the full Medicaid population (43.9% vs. 29.2%). This difference may have affected the results.
Limitations
This study has some limitations to consider. Administrative claims data are limited to the available information. Errors may include incorrect diagnoses or procedure codes, incorrect days supply, or inclusion of reversed claims. Prescriptions paid for out of pocket are also not reflected in data, although occurrence of this is thought to be minimal, since prescriptions for youth in this population do not have a copay or a limit on total monthly prescriptions. Also, relevant diagnosis and procedure codes included for consideration in the analysis were determined based on the clinical experience of the research team and stakeholders. Coding patterns may differ between states or regions. Coding for obesity may be underreported, particularly in younger children; therefore, obesity rates may be higher than reported.
Some variables in the administrative claims data are subject to self-reporting (e.g., race). Although coding used to determine appropriate service use was chosen by the stakeholder committee, it is possible that some service types were not included, and individuals may have received appropriate services but were not classified as such. Potential coding errors may also have been present within the analyses.
This review was limited largely to administrative claims data available through OHCA. Data were not reviewed longitudinally, which may have highlighted specific trends in psychotropic medication use. Some information, such as an individual’s time in foster care, was unavailable in the claims data for inclusion in the analysis. Medicaid programs are also different from state to state, so caution should be taken in generalizing findings to other foster children or Medicaid programs.
Conclusions
Determining appropriate psychotropic medication use in this population is challenging. Despite higher psychotherapy occurrence, rates of psychotropic medication use and concurrent multiclass psychotropic polypharmacy remain a concern in foster youth, and metabolic adverse effects were observed in this population. The ability to locate those at highest risk for high levels of psychotropic medication use in a timely fashion is key to ensuring that this population is receiving optimal care. Based on the presence of an antipsychotic at the highest level of polypharmacy, the addition of an antipsychotic to a regimen may be an important signal for additional monitoring. Longitudinal studies should be undertaken to explore factors associated with higher levels of psychotropic polypharmacy in foster youth and used to further assist in developing actionable interventions. Outcomes of multiclass psychotropic polypharmacy in foster youth, such as metabolic diseases, placement issues, and issues when foster kids age out of the system, should also be explored to further inform potential opportunities for policies.
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