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Objective To assess risks of mortality associated with use of individual antipsychotic drugs in elderly residents in nursing homes.
Design Population based cohort study with linked data from Medicaid, Medicare, the Minimum Data Set, the National Death Index, and a national assessment of nursing home quality.
Setting Nursing homes in the United States.
Participants 75445 new users of antipsychotic drugs (haloperidol, aripiprazole, olanzapine, quetiapine, risperidone, ziprasidone). All participants were aged ≥65, were eligible for Medicaid, and lived in a nursing home in 2001-5.
Main outcome measures Cox proportional hazards models were used to compare 180 day risks of all cause and cause specific mortality by individual drug, with propensity score adjustment to control for potential confounders.
Results Compared with risperidone, users of haloperidol had an increased risk of mortality (hazard ratio 2.07, 95% confidence interval 1.89 to 2.26) and users of quetiapine a decreased risk (0.81, 0.75 to 0.88). The effects were strongest shortly after the start of treatment, remained after adjustment for dose, and were seen for all causes of death examined. No clinically meaningful differences were observed for the other drugs. There was no evidence that the effect measure modification in those with dementia or behavioural disturbances. There was a dose-response relation for all drugs except quetiapine.
Conclusions Though these findings cannot prove causality, and we cannot rule out the possibility of residual confounding, they provide more evidence of the risk of using these drugs in older patients, reinforcing the concept that they should not be used in the absence of clear need. The data suggest that the risk of mortality with these drugs is generally increased with higher doses and seems to be highest for haloperidol and least for quetiapine.
Up to a third of all elderly patients in nursing homes are treated with antipsychotic drugs.1 2 3 4 5 In the past, inappropriate prescribing of antipsychotics in nursing homes has primarily been considered a marker of suboptimal care.6 7 Federal action thus focused primarily on defining and enforcing specific diagnostic criteria for the initiation and monitoring of these drugs (Omnibus Budget Reconciliation Act).8 In recent years, evidence has accumulated that their use is a drug safety issue as well. After earlier warnings of increased risks of cerebrovascular events (with risperidone, olanzapine, and aripiprazole),9 the Food and Drug Administration issued an advisory warning in 2005 that atypical antipsychotics were associated with a 60-70% increased risk of death compared with placebo in randomised controlled trials among older patients with dementia, and black box warnings were added to the labels of all atypical drugs.10 Subsequent studies found risks at least as high among users of conventional antipsychotics,11 12 13 and the Food and Drug Administration issued a similar warning for such drugs in 2008.14
Despite these strong safety warnings, use of antipsychotic drugs in nursing homes is likely to remain substantial—as evidenced by the recent audit by the US Department of Health and Human Services15—because of the continued growth in the number of people with dementia, the perceived need for some type of intervention in patients with severe persistent symptoms, and a paucity of effective alternative pharmacological or behavioural approaches.16 Questions about the comparative safety of individual antipsychotic drugs are therefore of paramount importance to patients and prescribers, but the existing Food and Drug Administration advisories do not distinguish between drugs in these classes and thus offer no guidance in that regard.
In the absence of randomised trials, surveillance data from large longitudinal healthcare databases provide a unique opportunity to examine the comparative safety of individual drugs, provided that rigorous methodological approaches are applied to minimise bias. Such databases also include the most vulnerable segments of the population, such as residents of nursing homes, who are commonly excluded from trials.
We investigated whether the risk of overall and cause specific mortality is equal across antipsychotic drugs or whether there are regimens with safety advantages that should be prescribed preferentially in older residents of nursing homes.
The study cohort was drawn from a merged dataset of Medicaid and Medicare claims, the minimum data set (MDS), the Online Survey Certification and Reporting (OSCAR) system, and the National Death Index in 45 states in the United States (all except Arizona, Delaware, Nevada, Oregon, and Rhode Island) for 2001-5. Claims data provided information on patients’ demographics, eligibility for Medicaid, physician services and admissions to hospital and their accompanying diagnoses, admissions to long term care, and filled prescriptions for drugs. The Minimum Data Set is a federally mandated health assessment tool used in nursing homes that captures information on physical, psychological, and psychosocial functioning, active clinical diagnoses, health conditions, treatments, and services. The Online Survey Certification and Reporting system is a uniform database of nursing home regulatory reviews, which is generated yearly for all nursing homes certified by the Centers for Medicare and Medicaid Services (CMS) and includes operational and staffing characteristics and aggregate resident characteristics.
Our cohort consisted of all patients aged ≥65 who were dually eligible for Medicare and Medicaid, who started treatment with an antipsychotic drug during a stay in a nursing home, and who had six months’ continuous Medicaid coverage before the date they started the antipsychotic drug (index date). Incident use required the absence of filled prescriptions for an antipsychotic in the six months before the index date. We used an incident user design to avoid underascertainment of events that occur soon after treatment begins17 and to ensure that baseline covariates at study entry were assessed before the start of treatment and were not affected by the treatment itself.18 Residents were excluded if they filled a prescription for both conventional and atypical antipsychotics on the index date and if they had a pre-existing diagnosis for cancer, schizophrenia, or bipolar disorder as these residents probably received antipsychotics for reasons other than behavioural problems related to dementia (fig 11).
Antipsychotic drugs considered include haloperidol, aripiprazole, olanzapine, quetiapine, risperidone, and ziprasidone. Other drugs (thioridazine, chlorpromazine, perphenazine, fluphenazine, acetophenazine, mesoridazine, promazine, trifluoperazine, triflupromazine, chlorprothixene, loxapine, molindone, pimozide, and thiothixene) were excluded because they were used by too few patients (1% for all combined) to permit interpretable estimation of the associations between drug and outcome (fig 11).). Each participant was assigned to a specific drug based on the first prescription; a given exposure was considered as discontinued if there was a gap in treatment of 14 days or more. We chose the most commonly used drug in this population, risperidone, as the reference drug. We converted daily doses of the index drug to equivalent doses of chlorpromazine (in mg)19 20 21 and used the median daily dose in the population (50 mg) as a cut off to assess the effect in groups of higher and lower doses (see table A in appendix on bmj.com). In dose-response analyses, we empirically defined cut offs for low, medium, and high dose groups for each individual drug after inspection of the dose distributions (see table B in appendix on bmj.com).
Information on vital status and causes of death was available through linkage with the National Death Index. We identified all deaths in the cohort within 180 days after the index date. We excluded deaths from cancer because such cancers were probably pre-existing and might have been associated with use of some drugs in this class to reduce nausea or to potentiate drugs for pain relief. As we recognise the potential for misclassification of causes of death in older populations,22 we examined the following groups of causes based on suggested pharmacological effects of antipsychotics23 24 25 26 27 and the Food and Drug Administration analysis10: diseases of the circulatory system (ICD-10 (international classification of diseases, 10th revision) codes I00-I99), cerebrovascular diseases (ICD-10 codes I60-I69), diseases of the respiratory system (ICD10 codes J00-J99), and all other causes combined.
We assessed characteristics of patients in the six months before cohort entry. Sociodemographic characteristics included age, sex, race, education, and geographical region (state). Clinical characteristics were determined according to the most recent Minimum Data Set assessment before the start of treatment, ICD-9 diagnostic and procedure codes associated with admissions to hospital and visits to physicians, and drug use. These variables assessed psychiatric morbidity, cardiovascular morbidity, cerebrovascular disease, Parkinson’s disease, epilepsy, diabetes, obesity, functional impairment, the Charlson index, and use of healthcare services potentially predictive of adverse health outcomes in the short term (number of days in hospital, number of distinct prescriptions for drugs excluding antipsychotics).28 We obtained characteristics of nursing homes, which could be correlated with care processes and risk of adverse health outcomes, from the Online Survey Certification and Reporting system. These included variables such as facility size, occupancy rate, availability of special care units, staffing levels, ownership, resident characteristics (for example, proportion with dementia, depression) and quality indicators (for example, proportion bedbound).
We compared distributions of sociodemographic, clinical, and use characteristics among participants who started taking different antipsychotics and calculated rates of mortality during follow-up. We censored follow-up at the time of discontinuation of treatment, augmentation, or switch to a different drug, and admission to hospital for 10 days or more, as treatment status is unknown during inpatient stays. To reduce the potential for informative censoring, we implemented a 30 day grace period. All deaths occurring during this time were attributed to the initial exposure.
We fitted proportional hazards models for pairwise comparisons against risperidone (unadjusted; adjusted for age, sex and calendar year; and adjusted for multiple variables). In multivariate analyses, we used propensity score adjustment to balance potential confounders.29 Propensity scores were derived from predicted probabilities of the start of treatment estimated in logistic regression models that contained all covariates listed above. Cox models were stratified across 10ths of the propensity score. In addition, we plotted multivariate adjusted Kaplan-Meier curves for survival as a function of the duration of use of the index antipsychotic using inverse probability of treatment weighting.30 In confirmatory analyses, we fitted high dimensional propensity scores,31 which have been shown to improve validity in claims data studies by further reducing residual confounding.32 33
We ran propensity score and outcome models separately in groups defined by recorded diagnoses of dementia and behavioural disturbances and by dose, dividing each group into those taking ≤50 mg or >50 mg chlorpromazine equivalents a day. A dose-response analysis was conducted to compare the risk of deaths from causes other than cancer in residents treated with high or medium versus low dose antipsychotics, for all drugs separately and combined. In sensitivity analyses, we estimated the strength of the residual confounding that would be required to fully explain the observed associations for deaths from causes other than cancer if in truth no such associations existed.34
From 2001 to 2005, 75445 older residents of nursing homes started treatment with antipsychotic drugs. Compared with the reference group risperidone, patients who started taking haloperidol were more likely at baseline to have cardiovascular disease, less likely to have psychiatric comorbidities, and had slightly worse general indicators of comorbidity. Patients who started taking risperidone had slightly fewer recorded diagnoses of depression and less use of antidepressants and other psychoactive drugs than patients who started treatment with other atypical antipsychotics. They also tended to have a lower use of cholinesterase inhibitors. Patients treated with quetiapine had more diagnoses of parkinsonism than the other groups, and patients treated with olanzapine had fewer diagnoses of diabetes. There were also some differences in the prescribing of specific drugs between regions and settings (table 11 and table C in appendix on bmj.com).
Eighty per cent of residents (n=60167) were censored before the end of 180 days. Discontinuation of treatment was the most common reason for censoring (57.2%, n=34388), followed by hospital admission for 10 days or longer (17.4%, n=10464), treatment switches or augmentation (13.1%, n=7902), and death (12.3%, n=7413). A total of 6598 residents died from causes other than cancer during the first 180 days after the start of treatment, yielding an event rate of 37.1 per 100 person years (95% confidence interval 36.2 to 38.0). Table 2 shows event rates for specific treatmentstreatments.
Findings from the Cox regression analyses indicated that, compared with risperidone, patients treated with haloperidol had double the risk of mortality (hazard ratio adjusted for propensity score 2.07, 95% confidence interval 1.89 to 2.26) and patients treated with quetiapine had a reduced risk (0.81, 0.75 to 0.88). No meaningful differences in risk were observed for aripiprazole, olanzapine, and ziprasidone (table 33).). Adjusted Kaplan-Meier plots are consistent with these findings (fig 22).). The effect of haloperidol was strongest during the first 40 days of treatment (hazard ratio adjusted for propensity score 2.34, 2.11 to 2.60) and reduced to 1.32 (1.02 to 1.71) and 1.46 (1.07 to 2.00) after 40-79 and 80-180 days of treatment, respectively. The corresponding rate ratios for quetiapine were 0.74 (0.66 to 0.82), 0.87 (0.75 to 1.01), and 0.91 (0.79 to 1.05). Analyses stratified by dose confirmed the overall findings (figs 33 and 44),), and we did not find evidence that the effect measure was modified by the presence of a recorded diagnosis of dementia or behavioural disturbances (see table D in appendix on bmj.com). Sensitivity analyses indicated that for an unmeasured confounder (such as frailty, severity of dementia) present in 25% of the population, relative risks ≥5.0 linking the hypothetical confounder to both haloperidol use and mortality would be needed to fully explain the observed association with mortality. For confounders present in 10% or 5% of the population, relative risks of >6.0 and 7.5, respectively, would be needed. To fully explain the protective association for quetiapine, relative risks of >2.5, 3.5, and 5.0 would be required for an unmeasured confounder present in 25%, 10%, and 5%, respectively, of the population (see figs A and B in appendix on bmj.com).
Almost half (49%, n=3262) of deaths were recorded as caused by circulatory disorders, 10% (n=655) by cerebrovascular diseases, and 15% (n=981) by respiratory disorders. Table 2 shows the cause specific event rates by treatment groupgroup.. The increased risk of death with haloperidol and the decreased risk with quetiapine were observed for all causes examined. Although no difference in overall mortality was observed for olanzapine, findings suggest a possibly lower risk of death from cerebrovascular diseases (hazard ratio adjusted for propensity score 0.88, 0.73 to 1.07; hazard ratio adjusted for high dimensional propensity score 0.83, 0.68 to 1.01). Given the relatively small number of patients treated with aripiprazole and ziprasidone, the associations for cause specific mortality are imprecisely estimated (table 33).
When we compared the risk of all deaths from causes other than cancer in residents treated with high versus low and medium versus low dose of a given drug, our findings suggest a dose-response relation for all antipsychotic drugs except quetiapine (fig 44).). The dose effects were most pronounced for haloperidol (hazard ratio adjusted for propensity score 1.84 for high and 1.40 for medium dose, both compared with low dose) and for risperidone (1.35 for high and 1.19 for medium dose).
In elderly residents receiving antipsychotic drugs in nursing homes, there is variation in the risk of death according to the type of drug used. Compared with risperidone users, haloperidol users had an increased risk and quetiapine users had a decreased risk of dying within 180 days. The effects were strongest shortly after the start of treatment and remained after adjustment for dose. No clinically meaningful differences were observed for the other drugs. There was no evidence that the treatment effect differed for patients with a diagnosis of dementia or behavioural disturbances. A dose-response relation was observed for all drugs, except quetiapine. The study was carried out in 75445 residents of nursing homes in 45 states in the US. All participants were aged ≥65, started treatment with antipsychotic drugs between 2001 and 2005, and were eligible for Medicaid.
Our results for haloperidol are consistent with the findings of observational studies that report a greater risk of death with conventional versus atypical antipsychotics in older adults,11 12 13 32 and the study by Liperoti et al, which found an increased risk with haloperidol compared with risperidone in patients with dementia in nursing homes in five US states (n=9729).35 Our finding of a reduced risk of death from causes other than cancer with quetiapine is compatible with an observation made by Rossom et al in a population of predominately male veterans with dementia.36 In contrast, Liperoti et al, using Minimum Data Set information to determine drug exposure, did not observe differences in mortality between individual atypical drugs.35
Another study that examined causes of death in elderly users of antipsychotics was done in British Columbia and found that those who started treatment with conventional rather than atypical antipsychotics had the highest relative risk of death from respiratory diseases (hazard ratio 1.71, 1.35 to 2.17), followed by circulatory disorders (1.23, 1.10 to 1.36).37 Our findings for haloperidol compared with risperidone in nursing home residents in the US mirror these results. Differences in cause specific mortality with atypical antipsychotic drugs have not previously been examined. Our comparative findings, however, are consistent with results reported in a recent meta-analysis that combined data from placebo controlled trials and found that the risk of cardiovascular outcomes in elderly patients with dementia was increased with risperidone and olanzapine but not with quetiapine. Likewise, risperidone, but not olanzapine or quetiapine, was found to be associated with an increased risk of stroke.38
A major strength of our study is the large population of residents in US nursing homes, which allowed us to examine the effect of individual drugs, different doses, and cause specific mortality. It was large enough to allow us to restrict our population to new users, which reduces the likelihood of missing early adverse events, allows for an evaluation of risks over duration of use, ensures that the assessment of baseline characteristics is not influenced by any effects of antipsychotic treatment, and reduces the likelihood that current treatment assignment is influenced by past experiences related to drugs, such as adverse events and refractory symptoms.17 To clearly identify exposure groups, we compared single drug treatments with each other and censored patient follow-up as soon as the patient switched drugs or augmented treatment with a second antipsychotic drug.
We looked at residual confounding by indication as an alternative explanation of our findings. This would occur if patients who were frail and at increased risk of death were more or less likely to be prescribed certain antipsychotic drugs. We supplemented confounder information derived from claims data with clinical assessment data (Minimum Data Set) and potential indicators of nursing home quality (Online Survey Certification and Reporting).39 We used multiple methods to mitigate confounding by the predefined covariates and by proxies for unobserved factors (adjustment for high dimensional propensity score31) and found results to be consistent. Sensitivity analyses showed that strong risk factors for death that are fairly imbalanced among exposure groups must be unmeasured and uncontrolled to explain the observed associations for deaths from causes other that cancer.
There is potential for misclassification of exposure status through lack of consumption of filled prescriptions. Patients in nursing homes are closely monitored, however, and adherence will be high, but occasional as-needed use might be an important source of misclassification. Patients were classified into groups with low and high doses according to the initial prescription. In case of dose adjustments, this could have resulted in misclassification of exposure in dose stratified analyses. Dose assignment, however, remained unchanged for over 90% of patients according to the second and last prescription filled before the end of follow-up. Results were also consistent when we used an alternative dose conversion algorithm.40
Broad categories of causes of death identified from death certificates have been found to agree with causes of death adjudicated by a physician, but problems arise when more specific subcategories of death—such as specific cardiovascular causes—are used.22 23 Although we examined only broad categories of causes of death, potential for misclassification remains, particularly in elderly people for whom the incidence of cardiovascular deaths tends to be overestimated,22 and we caution against overinterpretation of these aspects of the results.
Our study population consisted of patients eligible for Medicaid. This restriction should not affect the validity of our findings. The central issue determining internal validity is comparability between the subcohorts included, not whether the study sample is representative of patients in nursing homes overall. As long as socioeconomic status and its correlates do not modify the effect of antipsychotic drugs on short term mortality, the findings should also be generalisable (that is, externally valid).
Various environmental, psychosocial, and behavioural interventions have been developed to deal with behavioural disturbances in patients with dementia,41 but their effectiveness has not been rigorously studied42 and their implementation is often hampered by a lack of resources.43 Although such non-pharmacological interventions are nearly universally recommended as first line treatment,44 they are commonly insufficient in people with severe and persistent or recurrent symptoms. Consequently, most patients will be given a psychotropic drug at some point in their disease progression.9 16 In the absence of proved effective and safe alternative pharmacological treatments, it is likely that antipsychotic drugs will continue to be used widely, despite the fact that they have not been approved for this indication, their use cannot be justified as evidence based,38 and there are clear data confirming their associated risk.
The evidence provided in our study reinforces the important risks associated with the use of these drugs and underscores the need to try alternative means of dealing with behavioural problems in older patients with dementia. While our findings cannot tackle the efficacy-safety trade off involved in the decision to proceed with drug treatment for severe and refractory behavioural problems in people with dementia, they can contribute to decision making regarding treatment for clinicians considering use of antipsychotics in patients whose behavioural problems might themselves pose a risk to the patient or others. If the clinician faces a situation in which use of these drugs seems inevitable, our findings underscore the importance of always prescribing the lowest possible dose and of closely monitoring patients, especially shortly after the start of treatment. The evidence accumulated so far implies that use of haloperidol in this vulnerable population cannot be justified because of the excess harm. Quetiapine might be somewhat safer than other atypical drugs, but these findings will require replication in other studies.
Appendix: Extra tables (A-D) and figures (A and B)
Contributors: All authors were responsible for study concept and design. SC and SS acquired the data, which were analysed and interpreted by all authors. KFH drafted the manuscript, which was critically revised for important intellectual content by all authors. KFH, TG, RL, and SS did the statistical analysis. SC, JA, and SS gave administrative, technical, or material support. SS was the study supervisor, and KFH is guarantor.
Funding: This study was supported by AHRQ/FDA Award HS017918 and AHRQ Award HS016097. KFH and SS were partially funded by National Institute of Mental Health R01-MH078708. The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; and preparation, review, or approval of the manuscript.
Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/coi_disclosure.pdf (available on request from the corresponding author) and declare: no support from any organisation for the submitted work; no financial relationships with any organisations that might have an interest in the submitted work in the previous three years; no other relationships or activities that could appear to have influenced the submitted work.
Ethical approval: This study was approved by the Institutional Review Board of the Brigham and Women’s Hospital, the Partners Human Research Committee.
Data sharing: No additional data available.
Cite this as: BMJ 2012;344:e977