Objective: To compare treatment patterns and Medicaid spending between schizophrenia patients initiating once-monthly paliperidone palmitate (PP1M) and oral atypical antipsychotics (OAAs) within four comorbid populations: cardiovascular disease (CVD), diabetes, hypertension and obesity. Methods: Five-state Medicaid data identified comorbid adults with schizophrenia initiating PP1M or OAAs (index) from September 2009 balanced with inverse probability of treatment weighting. Chi-squared and t-tests compared index antipsychotic (AP) exposure (no gap >90 days) duration, AP polypharmacy, and index AP adherence (proportion of days covered >= 80%) and persistence (no gap >= 60 days) at 12 months post-index. Linear models with a non-parametric bootstrap procedure compared costs. Results: PP1M patients consistently had longer index AP exposure (e.g. CVD: 244 vs. 189 days; p < .001) and less AP polypharmacy (e.g. CVD: 21.1% vs. 28.1%; p < .001) versus OAA patients. Relative to OAA patients, adherence was more likely in PP1M patients with CVD or obesity (e.g. CVD: 28.6% vs. 22.1%; p < .001) and less likely for patients with diabetes (22.0% vs. 24.4%; p = .031). Persistence was consistently more likely for PP1M versus OAA patients (e.g. CVD: 49.9% vs. 27.4%; p < .001). Total costs were not significantly different between PP1M and OAA patients for any comorbidity. PP1M patients with diabetes, hypertension or obesity had higher pharmacy and lower medical costs (all p < .05). Conclusions: Treatment with PP1M versus OAAs may reduce AP polypharmacy and increase AP persistence in comorbid patients with schizophrenia, without increasing total healthcare costs. Comorbidities are a highly prevalent driver of excess mortality in this vulnerable population; thus, future studies should specifically address the real-world effectiveness of therapies, including long acting injectable therapies (LAIs), for these patients.
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Groupe d’analyse, Ltée, 1000 De La Gauchetière West, Suite 1200, Montréal, H3B 4W5, QCGroupe d’analyse, Ltée, 1000 De La Gauchetière West, Suite 1200, Montréal, H3B 4W5, QC
Lafeuille M.-H.
Tandon N.
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Janssen Scientific Affairs LLC, Titusville, NJGroupe d’analyse, Ltée, 1000 De La Gauchetière West, Suite 1200, Montréal, H3B 4W5, QC
Tandon N.
Tiggelaar S.
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Groupe d’analyse, Ltée, 1000 De La Gauchetière West, Suite 1200, Montréal, H3B 4W5, QCGroupe d’analyse, Ltée, 1000 De La Gauchetière West, Suite 1200, Montréal, H3B 4W5, QC
Tiggelaar S.
Kamstra R.
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Groupe d’analyse, Ltée, 1000 De La Gauchetière West, Suite 1200, Montréal, H3B 4W5, QCGroupe d’analyse, Ltée, 1000 De La Gauchetière West, Suite 1200, Montréal, H3B 4W5, QC
Kamstra R.
Lefebvre P.
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Groupe d’analyse, Ltée, 1000 De La Gauchetière West, Suite 1200, Montréal, H3B 4W5, QCGroupe d’analyse, Ltée, 1000 De La Gauchetière West, Suite 1200, Montréal, H3B 4W5, QC
Lefebvre P.
Kim E.
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Janssen Scientific Affairs LLC, Titusville, NJGroupe d’analyse, Ltée, 1000 De La Gauchetière West, Suite 1200, Montréal, H3B 4W5, QC
Kim E.
Yue Y.
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Janssen Scientific Affairs LLC, Titusville, NJGroupe d’analyse, Ltée, 1000 De La Gauchetière West, Suite 1200, Montréal, H3B 4W5, QC
Yue Y.
Joshi K.
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Janssen Scientific Affairs LLC, Titusville, NJGroupe d’analyse, Ltée, 1000 De La Gauchetière West, Suite 1200, Montréal, H3B 4W5, QC