Skip to main content
Full access
Articles
Published Online: 1 September 2012

Adherence to Antipsychotics and Cardiometabolic Medication: Association With Health Care Utilization and Costs

Abstract

Objective:

This study examined the association between adherence to antipsychotic and cardiometabolic medication and annual use of health care services and expenditures.

Methods:

MarketScan Medicaid files from 2004 to 2008 were used to evaluate annual cross-sections of patients with schizophrenia and diabetes, hypertension, or hyperlipidemia. Annual adherence to antipsychotic and cardiometabolic medication was defined as a score of at least 80% on proportion of days covered. Logistic regression was used to examine the association between antipsychotic adherence and adherence to cardiometabolic medications. Count data models and generalized linear models estimated health care utilization and health care expenditures, respectively, for outpatient, emergency, inpatient, and overall health services.

Results:

A total of 87,015 unique patients with schizophrenia received at least one antipsychotic medication. The overall prevalence of any comorbid cardiometabolic condition was 42.9% in 2004 and increased to 52.5% in 2008. Adherence to cardiometabolic medications was significantly greater among patients who were adherent to antipsychotic medications (adjusted odds ratio=6.9). Adjusted annual expenditures for emergency and inpatient care were higher for patients who were nonadherent to either antipsychotics or cardiometabolic medications than for patients who were adherent to antipsychotic and cardiometabolic medications. They were highest for patients who were nonadherent to both groups of medications. Outpatient, medication, and overall expenditures were lower for patients who were nonadherent to antipsychotic medications, regardless of cardiometabolic medication adherence.

Conclusions:

Among Medicaid patients with schizophrenia, cardiometabolic conditions are common, and adherence to antipsychotics and adherence to cardiometabolic medications are strongly related. Interventions that can improve medication adherence to treatment of both schizophrenia and comorbid cardiometabolic conditions may reduce emergency visits and hospitalizations. (Psychiatric Services 63:920–928, 2012; doi: 10.1176/appi.ps.201100328)
Schizophrenia affects more than 1.5 million people in the United States (1) and represents a significant economic burden. The annual costs of schizophrenia were estimated to be $62.7 billion in 2002 alone (2). Proper management of schizophrenia with antipsychotic drugs can improve symptoms and reduce disease burden (3). However, antipsychotic nonadherence is common (49) and is associated with increased emergency department visits, inpatient hospitalizations, and costs (5,1012). In the United States, costs of inpatient care related to antipsychotic nonadherence in 2005 were estimated to be nearly $1.5 billion (10).
By contributing to deficits in cognitive flexibility, concentration, and memory, antipsychotic nonadherence also has an impact on the treatment of other conditions (13,14). This effect is particularly concerning because patients with schizophrenia receive disproportionately worse general medical care and have poorer outcomes than patients with other mental illnesses (7,1518).
Nonadherence may be especially important in the self-management of cardiometabolic health conditions such as diabetes, hypertension, and hyperlipidemia (19,20) because coronary heart disease contributes to decreased life expectancy among patients with schizophrenia (21). The risk of cardiovascular mortality among patients with schizophrenia is roughly double the risk in the general population (22). Factors such as smoking, sedentary lifestyle, poor dietary habits, and obesity are believed to contribute to heart disease risk among patients with schizophrenia (23), but it is unclear whether nonadherence to antipsychotic treatment plays a role in cardiovascular health (24). Nonadherence to antipsychotics may have an adverse cascading impact on nonadherence to cardiometabolic medications, which is known to be related to increased risk of hospitalization and higher health care costs (25).
Previous studies have compared adherence across antipsychotics and medications for comorbid illnesses (9,13,26) and examined the relationship of antipsychotic nonadherence with hospitalizations, functional outcomes, and costs (10,2729). However, the relationship between antipsychotic adherence and adherence to cardiometabolic medications among patients with schizophrenia is unclear. One study reported that rates of adherence to antipsychotics and to nonpsychiatric medications are uncorrelated (9), a second study found a modest correlation between antipsychotic adherence and adherence to diabetes and antihypertensive medications (13), and another study found that antipsychotic nonadherence predicted nonadherence to diabetes medication (26).
This study assessed associations between antipsychotic adherence and adherence to cardiometabolic medication among patients with schizophrenia and at least one cardiometabolic condition. It also evaluated the association between adherence to antipsychotic and cardiometabolic medications and health care utilization and costs.

Methods

Study design and data

We conducted a cross-sectional time-series study from 2004 to 2008 of Medicaid patients with schizophrenia and comorbid cardiometabolic conditions. We chose a prevalent user cohort design to provide generalizable snapshots of a population of Medicaid beneficiaries that was large enough to enable sufficiently powered analyses of adherence, utilization, and expenditure patterns (3032).
Medicaid claims data were obtained from Thomson Reuters MarketScan Medicaid files, which contain details about enrollment, prescription claims, inpatient admissions, inpatient facility records, and outpatient claims for approximately seven million beneficiaries of multiple Medicaid programs. Specific states contributing data to Thomson Reuters are not identifiable.

Population selection

Patients with schizophrenia were defined as having one inpatient or two or more outpatient visits with ICD-9-CM codes 295.1–295.3, 295.6, or 295.9 during each annual cross-section (33). Patients who were dually enrolled in Medicare, younger than 18 or older than 64, not continuously enrolled in Medicaid during the year assessed, or without drug coverage for the entire year were excluded. Because we were interested in all patients with schizophrenia rather than just newly diagnosed or newly treated schizophrenia, we included patients that met inclusion criteria in any year. Patients could be counted in the analysis during more than one year because excluding patients after their first year of observation would have biased our sample toward patients earlier in their disease, especially during later years of the time period we studied. We restricted the sample to users of second-generation antipsychotics because they are the most commonly prescribed medications for schizophrenia. We excluded patients using long-acting injectable antipsychotics because of the challenges of measuring adherence to these products. The final sample represented annual snapshots of patients with schizophrenia using oral second-generation antipsychotics in 2004–2008.
Patients were further categorized on the basis of antipsychotic medication use; diagnoses of diabetes, hyperlipidemia, and hypertension; and use of medications to treat a cardiometabolic condition. Comorbid conditions were identified as having at least one inpatient or two outpatient claims for hypertension (ICD-9-CM codes 401.xx–405.xx), hyperlipidemia (272.xx), and diabetes (250.xx). Cardiometabolic medications included all oral medications for diabetes (metformin, sulfonylureas, thiazolidinediones, and other categories); statins for hyperlipidemia; and antihypertensive medications classified as angiotensin converting enzyme inhibitors, angiotensin II receptor blockers, beta blockers, calcium channel blockers, and diuretics, including loop, thiazide, and potassium-sparing categories of diuretic therapy (34).

Outcomes

The outcomes included medication adherence, utilization of health services for all causes, and expenditures for health services for all causes. Adherence to oral second-generation antipsychotics, oral antidiabetes medications, statins, and antihypertensives was measured as the proportion of days covered (PDC), which captures the number of days in a year without gaps in medication coverage divided by the number of days observed in the same year. The PDC measure has been shown to perform particularly well as a measure of adherence to antipsychotic medications by individuals with schizophrenia (35). The PDC measurement interval for a given patient began on the date of the first prescription observed of each medication in each year and continued through the end of that year. The days' supply of each prescription was added to the actual date that the prescription was dispensed to calculate the next scheduled fill date. Periods were considered gaps in the PDC metric if there was no medication available for any drug within each therapeutic class. This therapeutic class-based measure accommodated problems with measuring patient switching and the use of two or more medications simultaneously but may overestimate actual adherence. The PDC ranges from 0 to 1, with 0 representing no medication use and 1 representing perfect adherence (36). Patients were designated as adherent or nonadherent by using a PDC cut-point of .8, which has been shown previously to predict health outcomes resulting from adherence (37).
No classes of second-generation antipsychotics, including low-dose quetiapine, were excluded. Adherence to cardiometabolic medication by the pooled cardiometabolic cohort was calculated as an unweighted average of PDC of the three classes of cardiometabolic drugs.
Health service utilization outcomes included annual counts of outpatient visits for all causes, emergency visits, and inpatient admissions. Health services were identified as unique visits per date of service to any provider. Health expenditure outcomes included payments for prescriptions and for inpatient, outpatient, and emergency visits during each year. Health expenditures were inflation-adjusted to 2008 dollars.

Explanatory variables

The explanatory variable of interest was adherence to antipsychotics. We controlled for age group (18–34, 35–54, and 55 and older), race (white non-Hispanic, black non-Hispanic, and other or missing), male gender, Charlson Comorbidity Index (CCI) score (38), and Medicaid eligibility that was due to blindness or disability. Possible scores on the CCI range from 0 to 30, with higher scores indicating more comorbidity and, therefore, greater risk of one-year mortality. We also controlled for characteristics of the Medicaid plan that provided a prescription copayment for antipsychotics, provider capitation, and state mental health substance abuse treatment coverage. In addition, we controlled for having a history of visits to a psychiatrist or for psychotherapy at baseline as a proxy for schizophrenia severity. Finally, we constructed indicators for type of second-generation antipsychotic initiated, which allowed us to control for patterns of antipsychotic pharmacotherapy.

Statistical analysis

We evaluated adherence to antipsychotic medications and cardiometabolic medications by patients in each annual cross-section and by patients pooled across all years. We also compared adherence to medications among patients by demographic characteristics, treatment, and comorbid condition for each annual cross-section and in a pooled population. For unadjusted and regression analyses, we partitioned the sample into four groups: adherent to antipsychotics and cardiometabolic medications, adherent to antipsychotics and nonadherent to cardiometabolic medications, nonadherent to antipsychotics and adherent to cardiometabolic medications, and nonadherent to both antipsychotics and cardiometabolic medications. Comparisons across the four groups were made by using t tests for continuous variables and chi square tests for categorical variables.
The unadjusted mean number of emergency visits, inpatient admissions, and outpatient visits per year by the four adherence groups were compared. Similarly, unadjusted total payments for these services as well as for prescription drugs were assessed by using descriptive and bivariate statistics. The likelihood of inpatient admissions and emergency visits was estimated with random effects logistic regression. Results are reported as odds ratios. The number of emergency visits, outpatient visits, and inpatient hospitalizations was estimated with random-effects negative binomial regression to account for the overdispersion of these outcomes.
To examine the relationship between the four adherence groups and expenditures for services, we prepared generalized estimating equations (GEEs) that accounted for the proportion of the groups that did not use the service and the distribution of users of the service among the four adherence groups. Outpatient, medication, and overall expenditures were estimated by using one-part GEEs with gamma distributions and log link functions to account for kurtosis. Inpatient and emergency expenditures were estimated by using two-part GEEs to account for the high proportion of nonusers. For the first-part model that estimated the probability of using emergency services or of being admitted, we estimated GEEs with a binomial distribution and logit link function. For the second-part model that estimated the level of expenditures among users, we estimated GEEs with gamma distributions and log link functions. All expenditure outcomes are reported as inflation-adjusted dollars for the exponentiated linear prediction.
Each regression adjusted for age, sex, race, capitation, use of medication copay, use of psychotherapy, use of psychiatrist, coverage of mental health and substance abuse treatment services, specific antipsychotic medications, CCI score, number of comorbid metabolic conditions (diabetes, hyperlipidemia, and hypertension), and calendar year. For all outcomes, a sensitivity analysis considered patients with comorbid diabetes, patients with comorbid hypertension, and patients with comorbid hyperlipidemia. [The results of the analysis are available online as a data supplement to this report.]
Specifically for the expenditure models, two additional sensitivity analyses explored whether conclusions were robust in relation to our sampling approach or covariate adjustment. [The results of the analyses are available in an online appendix to this report.]
The first sensitivity analysis excluded patients in capitated plans and patients with no coverage for mental health and substance abuse treatment services because these factors may influence expenditures. The second sensitivity analysis used this restricted sample but also removed covariates for visits with a psychiatrist and use of psychotherapy because these variables might reflect behaviors associated with medication adherence. This model also removed cardiometabolic cohort count indicators that measured the number of cardiometabolic conditions of each patient. Removing these indicators explored the potential that we might be overadjusting regression models by counting comorbidity with both the CCI and the cardiometabolic condition count indicator.
All analyses represent associations because our use of a time-series design with a cross-section of prevalent users did not allow us to control for temporal relationships between adherence behaviors and use of services. Human subjects approval was obtained from the Western Institutional Review Board, an independent commercial institutional review board located in Olympia, Washington.

Results

We identified 87,015 unique patients with schizophrenia taking at least one antipsychotic medication between 2004 and 2008. Of these, 14.2% (N=12,349) had diabetes, 28.6% (N=24,843) had hypertension, and 12.5% (N=10,909) had hyperlipidemia. The overall prevalence of any comorbid cardiometabolic condition was 42.9% (N=9,169) in 2004 and increased steadily to 52.1% (N=9,001) in 2008. [Further details about the sample are available in an online appendix to this report.]
A total of 33,230 (38%) patients used cardiometabolic medications for diabetes, hyperlipidemia, or hypertension (Table 1). The mean±SD age was 48±10 years, 43% (N=14,217) were male, and 53% (N=17,551) were black. Hypertension was the most common of the treated comorbidities (N=24,843, 75%), followed by diabetes (N=12,349, 37%) and hyperlipidemia (N=10,909, 33%). Most (N=20,948, 63%) patients had just one of the three comorbid conditions; 9,693 (29%) had two conditions, and 2,589 (8%) had all three conditions. Statistically significant differences (p<.05) among the four adherence groups for nearly all covariates were found. Differences between the groups in sex, race, capitated insurance coverage, psychotherapy use, rates of hyperlipidemia and hypertension, and antipsychotic copay were noteworthy.
Over all years, 65.2% (N=21,665) of antipsychotic users were classified as adherent. Among patients prescribed a cardiometabolic drug, 60.6% (N=7,480) of patients prescribed diabetes medication, 59.5% (N=14,774) of those prescribed antihypertensives, and 61.6% (N=6,717) of those prescribed antihyperlipidemics were classified as adherent to the cardiometabolic medication. Among patients in the pooled sample, the odds of being adherent to cardiometabolic medications were significantly greater among patients who were adherent to antipsychotics than among patients who were not (AOR=6.9, 95% confidence interval [CI]=6.4–7.4) (Figure 1). The AORs comparing antipsychotic adherence among patients who were or were not adherent to cardiometabolic medication were 12.7 for diabetes medications, 9.2 for antihyperlipidemic medications, and 11.5 for antihypertensive medications.
The adjusted number of emergency visits and inpatient admissions was roughly double among the patients who were not adherent to antipsychotics compared with the adherent group (Table 2), but the adherent group had more outpatient visits. Expenditures paralleled this pattern. Mean unadjusted one-year total expenditures were highest for the group that was fully adherent to antipsychotics and cardiometabolic medications ($30,847) and lowest for the group that was fully nonadherent to antipsychotics and cardiometabolic medications ($20,757).
Patients who were adherent to antipsychotic and cardiometabolic medications were modeled as the reference group in analyses comparing health care service use and costs among the other adherence groups (Table 3). In these analyses, relatively infrequent outcomes such as emergency visits and inpatient admissions were first modeled as the risk of having a visit among all patients. Subsequent analyses estimated the number of visits and expenditures among users compared with the fully adherent group. Because outpatient visits were relatively common, only the number of visits and expenditures were modeled. Medication expenditures and total expenditures were modeled for all patients.
Patients who were nonadherent to both drug types had the greatest increase in risk of emergency visits (adjusted odds ratio [AOR]=3.9) and inpatient admissions (AOR=4.0). Smaller but significant increases in risk of emergency visits and inpatient admissions were observed for patients who were adherent to antipsychotics but not cardiometabolic medications (emergency visits, AOR=1.9; inpatient admissions, AOR=2.2) as well as for patients who were nonadherent to antipsychotic medications but adherent to cardiometabolic medications (emergency visits, AOR=2.1; inpatient admissions (AOR=2.1).
Adjusted annual expenditures for emergency visits and inpatient admissions were higher for patients who were nonadherent to either antipsychotic or cardiometabolic medications and were highest for the patients who were nonadherent to both groups of medications. Expenditures for emergency visits ($668), inpatient admissions ($5,857), outpatient visits (−$2,749), and medication (−$3,099) were lower for fully nonadherent patients than for patients adherent to antipsychotic and cardiometabolic medications. Overall health care expenditures were lower for patients who were adherent to neither cardiometabolic or antipsychotic medications (−$1,128) and for patients who were adherent to cardiometabolic medications but not antipsychotic medications (−$1,467). Results did not statistically significantly change in sensitivity analyses of the sampling approach and covariate adjustment.

Discussion

Approximately 36% of patients with schizophrenia in our sample were classified as nonadherent to antipsychotic medication, which is lower than the 50% nonadherence rate reported in the literature (49). We also found that adherence to antipsychotics and adherence to cardiometabolic medications were strongly related. The magnitude of the association of antipsychotic adherence and cardiometabolic medication adherence observed in our study (OR=6.9, p<.001) was larger than the association observed in two previous studies of antipsychotics, antidiabetics, and antihypertensives (9,13), but the direction of the associations was relatively consistent.
The possible implications of antipsychotic nonadherence are particularly interesting, especially given the strong relationship between antipsychotic and cardiometabolic nonadherence. Our results suggest that antipsychotic nonadherence may contribute substantially to emergency visits and hospitalizations. Compared with patients who were adherent to both antipsychotics and medications for cardiometabolic conditions, patients who were nonadherent to one or more classes had a higher likelihood of emergency visits and a hospitalization.
Health care expenditures were similar for patients who were adherent to antipsychotics but nonadherent to cardiometabolic medications and for fully adherent patients. Patients who were nonadherent to antipsychotics and adherent to medications for cardiometabolic conditions had lower overall health care expenditures than fully adherent patients. Although this is partly accounted for by reduced medication costs and fewer outpatient visits associated with schizophrenia management, antipsychotic nonadherence was associated with a greater increase in emergency visits and inpatient care than was cardiometabolic medication nonadherence. Emergency visits and inpatient costs of the fully nonadherent group were even more dramatically increased, illustrating the compounded effects of nonadherence.
Patients who were adherent to antipsychotics were at reduced risk for use of acute, costly services, including emergency visits and inpatient admissions, which translated into lower expenditures for these services. Our finding is consistent with several previous studies (5,1012). Reduced health service utilization and lower health expenditures may be indicative of better drug treatment, which could reduce the need for intensive health care resources (use of emergency or inpatient facilities). However, patients who adhered to antipsychotic medication had significantly more outpatient visits, and their drug expenditures were proportionally higher because of their better adherence. These higher costs more than offset the lower emergency and inpatient expenditures.
The higher outpatient service utilization of patients who were adherent to antipsychotic medications may be related to behavioral or disease management factors. For example, it might be reflective of the need to closely monitor antipsychotic treatments. Consensus guidelines recommend monthly to quarterly monitoring of weight, blood pressure, blood sugar, and lipids to avoid the potential adverse effects of antipsychotic medications (39). Because we cannot be certain our findings were related to these factors, nor differentiate which expenditures were attributed to psychiatric or cardiometabolic factors, future studies should explore the sources of increased expenditures by types of nonadherence.
Three plausible reasons may explain the increased prevalence, from 43% to 53%, of cardiometabolic conditions over a five-year period. First, the uptick might be reflective of underlying changes in the Medicaid population that were not captured in our data. We observed a significant reduction in the schizophrenia population from 2006 (N=20,723) to 2007 (N=16,910), which may reflect changes in state eligibility requirements that were not captured in our data. These changes could influence the severity of mental illness among patients diagnosed as having schizophrenia or the cardiometabolic risk of patients with schizophrenia. Second, increasing attention to cardiometabolic risk from research such as the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) may have increased rates of screening for cardiometabolic conditions among antipsychotic users (40). This would represent an increase in diagnosis and treatment of previously undiagnosed conditions, not necessarily an increase in the prevalence of these conditions.
Finally, an actual increase in the risk of cardiometabolic effects resulting from antipsychotic medication use might be a contributor. Antipsychotic medications, and in particular second-generation antipsychotic agents, have been linked to weight gain, disruptions in glucose metabolism, diabetes, hypertension, and hyperlipidemia (40,41). Growing concern and management of these potential problems might also have increased diagnosis or treatment of cardiometabolic conditions.
This study had several limitations. First, we did not examine the temporal relationship between antipsychotic and cardiometabolic medication adherence in our annual cross-sections. Further, our pooling of annual cross-sections of patients likely resulted in counting some patients more than once, allowing their adherence and service use to vary by year. We controlled for year in our analyses, but we were unable to adjust for individual-level clustering of observations, which could result in modestly smaller confidence intervals for our estimates.
Second, a primary outcome in this study was medication adherence, which was measured using pharmacy administrative claims data. Use of these data to measure adherence assumes that patients who obtain medications actually take them. Third, by virtue of requiring drug use, our study population could be biased to reflect more adherent patients. This phenomenon could be reflected in measures of adherence to both antipsychotic and cardiometabolic medication. Fourth, our measurement of health care utilization and expenditures covered only relatively short, one-year intervals. Given the likely long-term benefits of antipsychotic and cardiometabolic medication adherence, it is possible we underestimated the positive effects and long-term cost reductions associated with being adherent.
Fifth, adherence may be affected by the types of services and expenditures patients receive for treatment of schizophrenia and cardiometabolic conditions, but we did not attempt to differentiate adherence rates by categories of services and expenditures. Finally, unobservable factors could have influenced our study findings. For example, patient self-efficacy (a belief that medication adherence will improve one's health) or social support may influence the decision to use both antipsychotic and cardiometabolic medications. Future studies could use primary data collection to capture the influence of other variables on the relationships examined by this study.
Our study supports the need for interventions targeting medication adherence by patients with schizophrenia and comorbid cardiometabolic conditions. Such interventions might specifically target patients who have demonstrated problems with adherence and have the potential to improve medication adherence by Medicaid patients with schizophrenia and comorbid cardiometabolic conditions. Such adherence improvement might translate into reduced use of emergency visits and inpatient admissions (42). Approaches that use pharmacy claims to screen for nonadherence may be one option, given that these approaches have been shown to efficiently and accurately identify patients at risk (5,43).

Conclusions

Based on analysis of annual cross-sections of Medicaid patients with schizophrenia, comorbid cardiometabolic conditions are common, and adherence with medications used to treat these conditions is strongly correlated with antipsychotic adherence. Nonadherent patients are at increased risk of use of emergency services and hospitalization. Average one-year costs are higher for adherent compared with nonadherent patients because of medication and outpatient expenditures, but longer-term cost implications of adherence should be explored by future studies.

Acknowledgments and disclosures

This study was funded by Novartis Pharmaceuticals Corporation. Dr. Maciejewski is a recipient of Research Career Scientist award RCS 10-391 from the U.S. Department of Veterans Affairs. The authors acknowledge the helpful comments of Christopher Zacker, Ph.D., during the early stages of manuscript preparation.
Dr. Hansen, Dr. Maciejewski, and Dr. Farley have served as consultants to Takeda Pharmaceuticals, Inc., and Novartis. Dr. Maciejewski owns stock in Amgen. Dr. Farley has received unrestricted grant support from Pfizer and the Robert Wood Johnson Foundation. At the time of this research, Dr. Yu-Isenberg was with Novartis Pharmaceutical Corporation and is now with GlaxoSmithKline.

Supplementary Material

File (pss6309_0920_ds.pdf)
Supplemental material

References

1.
Wu EQ, Shi L, Birnbaum H, et al.: Annual prevalence of diagnosed schizophrenia in the USA: a claims data analysis approach. Psychological Medicine 36:1535–1540, 2006
2.
Wu EQ, Birnbaum HG, Shi L, et al.: The economic burden of schizophrenia in the United States in 2002. Journal of Clinical Psychiatry 66:1122–1129, 2005
3.
Lehman AF, Lieberman JA, Dixon LB, et al.: Practice guideline for the treatment of patients with schizophrenia, second edition. American Journal of Psychiatry 161:1–56, 2004
4.
McCombs JS, Nichol MB, Stimmel GL, et al.: Use patterns for antipsychotic medications in Medicaid patients with schizophrenia. Journal of Clinical Psychiatry 60(suppl 19):5–11, 1999
5.
Valenstein M, Copeland LA, Blow FC, et al.: Pharmacy data identify poorly adherent patients with schizophrenia at increased risk for admission. Medical Care 40:630–639, 2002
6.
Lacro JP, Dunn LB, Dolder CR, et al.: Prevalence of and risk factors for medication nonadherence in patients with schizophrenia: a comprehensive review of recent literature. Journal of Clinical Psychiatry 63:892–909, 2002
7.
Gilmer TP, Dolder CR, Lacro JP, et al.: Adherence to treatment with antipsychotic medication and health care costs among Medicaid beneficiaries with schizophrenia. American Journal of Psychiatry 161:692–699, 2004
8.
Dolder CR, Lacro JP, Dunn LB, et al.: Antipsychotic medication adherence: is there a difference between typical and atypical agents? American Journal of Psychiatry 159:103–108, 2002
9.
Dolder CR, Lacro JP, Jeste DV: Adherence to antipsychotic and nonpsychiatric medications in middle-aged and older patients with psychotic disorders. Psychosomatic Medicine 65:156–162, 2003
10.
Sun SX, Liu GG, Christensen DB, et al.: Review and analysis of hospitalization costs associated with antipsychotic nonadherence in the treatment of schizophrenia in the United States. Current Medical Research and Opinion 23:2305–2312, 2007
11.
Haywood TW, Kravitz HM, Grossman LS, et al.: Predicting the “revolving door” phenomenon among patients with schizophrenic, schizoaffective, and affective disorders. American Journal of Psychiatry 152:856–861, 1995
12.
Sullivan G, Wells KB, Morgenstern H, et al.: Identifying modifiable risk factors for rehospitalization: a case-control study of seriously mentally ill persons in Mississippi. American Journal of Psychiatry 152:1749–1756, 1995
13.
Piette JD, Heisler M, Ganoczy D, et al.: Differential medication adherence among patients with schizophrenia and comorbid diabetes and hypertension. Psychiatric Services 58:207–212, 2007
14.
Jeste SD, Patterson TL, Palmer BW, et al.: Cognitive predictors of medication adherence among middle-aged and older outpatients with schizophrenia. Schizophrenia Research 63:49–58, 2003
15.
Folsom DP, McCahill M, Bartels SJ, et al.: Medical comorbidity and receipt of medical care by older homeless people with schizophrenia or depression. Psychiatric Services 53:1456–1460, 2002
16.
Druss BG, Bradford WD, Rosenheck RA, et al.: Quality of medical care and excess mortality in older patients with mental disorders. Archives of General Psychiatry 58:565–572, 2001
17.
Weiss AP, Henderson DC, Weilburg JB, et al.: Treatment of cardiac risk factors among patients with schizophrenia and diabetes. Psychiatric Services 57:1145–1152, 2006
18.
Dolder CR, Furtek K, Lacro JP, et al.: Antihypertensive medication adherence and blood pressure control in patients with psychotic disorders compared to persons without psychiatric illness. Psychosomatics 46:135–141, 2005
19.
Correll CU, Druss BG, Lombardo I, et al.: Findings of a US national cardiometabolic screening program among 10,084 psychiatric outpatients. Psychiatric Services 61:892–898, 2010
20.
Nasrallah HA, Meyer JM, Goff DC, et al.: Low rates of treatment for hypertension, dyslipidemia and diabetes in schizophrenia: data from the CATIE schizophrenia trial sample at baseline. Schizophrenia Research 86:15–22, 2006
21.
Hennekens CH, Hennekens AR, Hollar D, et al.: Schizophrenia and increased risks of cardiovascular disease. American Heart Journal 150:1115–1121, 2005
22.
Brown S, Inskip H, Barraclough B: Causes of the excess mortality of schizophrenia. British Journal of Psychiatry 177:212–217, 2000
23.
Goff DC, Cather C, Evins AE, et al.: Medical morbidity and mortality in schizophrenia: guidelines for psychiatrists. Journal of Clinical Psychiatry 66:183–194, 2005
24.
Stahl SM, Mignon L, Meyer JM: Which comes first: atypical antipsychotic treatment or cardiometabolic risk? Acta Psychiatrica Scandinavica 119:171–179, 2009
25.
Sokol MC, McGuigan KA, Verbrugge RR, et al.: Impact of medication adherence on hospitalization risk and health care cost. Medical Care 43:521–530, 2005
26.
Nelson LA, Graham MR, Lindsey CC, et al.: Adherence to antihyperlipidemic medication and lipid control in diabetic Veterans Affairs patients with psychotic disorders. Psychosomatics 52:310–318, 2011
27.
Knapp M, King D, Pugner K, et al.: Non-adherence to antipsychotic medication regimens: associations with resource use and costs. British Journal of Psychiatry 184:509–516, 2004
28.
Ascher-Svanum H, Faries DE, Zhu B, et al.: Medication adherence and long-term functional outcomes in the treatment of schizophrenia in usual care. Journal of Clinical Psychiatry 67:453–460, 2006
29.
Ward A, Ishak K, Proskorovsky I, et al.: Compliance with refilling prescriptions for atypical antipsychotic agents and its association with the risks for hospitalization, suicide, and death in patients with schizophrenia in Quebec and Saskatchewan: a retrospective database study. Clinical Therapeutics 28:1912–1921, 2006
30.
Beebe LH, Smith K, Crye C, et al.: Telenursing intervention increases psychiatric medication adherence in schizophrenia outpatients. Journal of the American Psychiatric Nurses Association 14:217–224, 2008
31.
Weiden P, Aquila R, Standard J: Atypical antipsychotic drugs and long-term outcome in schizophrenia. Journal of Clinical Psychiatry 57(suppl 11):53–60, 1996
32.
Nicholl D, Akhras KS, Diels J, et al.: Burden of schizophrenia in recently diagnosed patients: healthcare utilisation and cost perspective. Current Medical Research and Opinion 26:943–955, 2010
33.
Lurie N, Popkin M, Dysken M, et al.: Accuracy of diagnoses of schizophrenia in Medicaid claims. Hospital and Community Psychiatry 43:69–71, 1992
34.
Briesacher BA, Andrade SE, Fouayzi H, et al.: Comparison of drug adherence rates among patients with seven different medical conditions. Pharmacotherapy 28:437–443, 2008
35.
Karve S, Cleves MA, Helm M, et al.: Prospective validation of eight different adherence measures for use with administrative claims data among patients with schizophrenia. Value in Health 12:989–995, 2009
36.
Benner JS, Glynn RJ, Mogun H, et al.: Long-term persistence in use of statin therapy in elderly patients. JAMA 288:455–461, 2002
37.
Karve S, Cleves MA, Helm M, et al.: Good and poor adherence: optimal cut-point for adherence measures using administrative claims data. Current Medical Research and Opinion 25:2303–2310, 2009
38.
Quan H, Sundararajan V, Halfon P, et al.: Coding algorithms for defining comorbidities in ICD-9-CM and ICD-10 administrative data. Medical Care 43:1130–1139, 2005
39.
American Diabetes Association American Psychiatric Association, American Association of Clinical Endocrinologists, et al.: Consensus development conference on antipsychotic drugs and obesity and diabetes. Journal of Clinical Psychiatry 65:267–272, 2004
40.
Lieberman JA, Stroup TS, McEvoy JP, et al.: Effectiveness of antipsychotic drugs in patients with chronic schizophrenia. New England Journal of Medicine 353:1209–1223, 2005
41.
Starrenburg FC, Bogers JP: How can antipsychotics cause diabetes mellitus? Insights based on receptor-binding profiles, humoral factors and transporter proteins. European Psychiatry 24:164–170, 2009
42.
Zygmunt A, Olfson M, Boyer CA, et al.: Interventions to improve medication adherence in schizophrenia. American Journal of Psychiatry 159:1653–1664, 2002
43.
Hansen RA, Dusetzina SB, Dominik RC, et al.: Prescription refill records as a screening tool to identify antidepressant non-adherence. Pharmacoepidemiology and Drug Safety 19:33–37, 2010

Figures and Tables

Figure 1 Adherence to medications for hypertension, hyperlipidemia, and diabetes and to antipsychotics among patients with schizophrenia
Table 1 Adherence to antipsychotics and medication for comorbid cardiometabolic conditions by 33,230 Medicaid patients, 2004–2008
Table 2 Annual utilization and expenditures for health care services among 33,230 patients, by adherence to antipsychotics and medications for cardiometabolic conditions, 2004–2008
Table 3 Annual use of health care services by patients who were nonadherent to antipsychotics or cardiometabolic medications, 2004–2008

Information & Authors

Information

Published In

Go to Psychiatric Services
Go to Psychiatric Services
Cover: Candy Apples, by Wayne Thiebaud, 1964/1990. Watercolor over hand-ground and dry-point etching, 5 × 5 inches. Gift of Mr. and Mrs. Paul LeBaron Thiebaud, 1996.19. Kemper Museum of Contemporary Art, Kansas City, Missouri.
Psychiatric Services
Pages: 920 - 928
PubMed: 22706887

History

Published online: 1 September 2012
Published in print: September 2012

Authors

Details

Richard A. Hansen, Ph.D.
Dr. Hansen is affiliated with the Department of Pharmacy Care Systems, Auburn University, 207 Dunstan Hall, Auburn, AL 36849 (e-mail: [email protected]). Dr. Maciejewski is with the Division of General Internal Medicine, Duke University, and with the U.S. Department of Veterans Affairs Medical Center, both in Durham, North Carolina. At the time of the research, Dr. Yu-Isenberg was with Novartis Pharmaceutical Corporation, East Hanover, New Jersey, and is now with GlaxoSmithKline, Research Triangle Park, North Carolina. Dr. Farley is with the UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill.
Matthew Maciejewski, Ph.D.
Dr. Hansen is affiliated with the Department of Pharmacy Care Systems, Auburn University, 207 Dunstan Hall, Auburn, AL 36849 (e-mail: [email protected]). Dr. Maciejewski is with the Division of General Internal Medicine, Duke University, and with the U.S. Department of Veterans Affairs Medical Center, both in Durham, North Carolina. At the time of the research, Dr. Yu-Isenberg was with Novartis Pharmaceutical Corporation, East Hanover, New Jersey, and is now with GlaxoSmithKline, Research Triangle Park, North Carolina. Dr. Farley is with the UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill.
Kristina Yu-Isenberg, Ph.D., M.P.H.
Dr. Hansen is affiliated with the Department of Pharmacy Care Systems, Auburn University, 207 Dunstan Hall, Auburn, AL 36849 (e-mail: [email protected]). Dr. Maciejewski is with the Division of General Internal Medicine, Duke University, and with the U.S. Department of Veterans Affairs Medical Center, both in Durham, North Carolina. At the time of the research, Dr. Yu-Isenberg was with Novartis Pharmaceutical Corporation, East Hanover, New Jersey, and is now with GlaxoSmithKline, Research Triangle Park, North Carolina. Dr. Farley is with the UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill.
Joel F. Farley, Ph.D.
Dr. Hansen is affiliated with the Department of Pharmacy Care Systems, Auburn University, 207 Dunstan Hall, Auburn, AL 36849 (e-mail: [email protected]). Dr. Maciejewski is with the Division of General Internal Medicine, Duke University, and with the U.S. Department of Veterans Affairs Medical Center, both in Durham, North Carolina. At the time of the research, Dr. Yu-Isenberg was with Novartis Pharmaceutical Corporation, East Hanover, New Jersey, and is now with GlaxoSmithKline, Research Triangle Park, North Carolina. Dr. Farley is with the UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill.

Metrics & Citations

Metrics

Citations

Export Citations

If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Simply select your manager software from the list below and click Download.

For more information or tips please see 'Downloading to a citation manager' in the Help menu.

Format
Citation style
Style
Copy to clipboard

View Options

View options

PDF/EPUB

View PDF/EPUB

Login options

Already a subscriber? Access your subscription through your login credentials or your institution for full access to this article.

Personal login Institutional Login Open Athens login
Purchase Options

Purchase this article to access the full text.

PPV Articles - Psychiatric Services

PPV Articles - Psychiatric Services

Not a subscriber?

Subscribe Now / Learn More

PsychiatryOnline subscription options offer access to the DSM-5-TR® library, books, journals, CME, and patient resources. This all-in-one virtual library provides psychiatrists and mental health professionals with key resources for diagnosis, treatment, research, and professional development.

Need more help? PsychiatryOnline Customer Service may be reached by emailing [email protected] or by calling 800-368-5777 (in the U.S.) or 703-907-7322 (outside the U.S.).

Media

Figures

Other

Tables

Share

Share

Share article link

Share