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Original Investigation
June 26, 2024

Pneumonia Risk, Antipsychotic Dosing, and Anticholinergic Burden in Schizophrenia

Author Affiliations
  • 1Department of Psychiatry, Amsterdam University Medical Center, Amsterdam, the Netherlands
  • 2GGZ inGeest Mental Health Care, Amsterdam, the Netherlands
  • 3Neuroscience Mood, Anxiety, Psychosis, Stress & Sleep Research Program, Amsterdam University Medical Center, Amsterdam, the Netherlands
  • 4Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University Medical Center, Maastricht, the Netherlands
  • 5Public Health Mental Health Research Program, Amsterdam University Medical Center, Amsterdam, the Netherlands
  • 6Department of Psychiatry, the Zucker Hillside Hospital, Northwell Health, Glen Oaks, New York
  • 7Department of Psychiatry and Molecular Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York
  • 8Department of Child and Adolescent Psychiatry, Charité Universitätsmedizin Berlin, Berlin, Germany
  • 9Department of Psychiatry, Hofstra/Northwell School of Medicine, Hempstead, New York
  • 10Department of Medicine, Hofstra/Northwell School of Medicine, Hempstead, New York
  • 11South Oaks Hospital, Northwell Health System, Amityville, New York
  • 12Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden
  • 13Department of Forensic Psychiatry, University of Eastern Finland, Niuvanniemi Hospital, Kuopio, Finland
  • 14Public Health Solutions, National Institute for Health and Welfare, Helsinki, Finland
  • 15Department of Psychiatry, Psychotherapy and Psychosomatics, Faculty of Medicine, University of Augsburg, Augsburg, Germany
  • 16German Center for Mental Health, München, Germany
  • 17Center for Psychiatric Research, Stockholm City Council, Stockholm, Sweden
  • 18School of Pharmacy, University of Eastern Finland, Kuopio, Finland
JAMA Psychiatry. 2024;81(10):967-975. doi:10.1001/jamapsychiatry.2024.1441
Key Points

QuestionÌý What antipsychotics are associated with pneumonia, which is the fourth leading cause of death in patients with schizophrenia?

FindingsÌý In this cohort study of 61 889 people with schizophrenia, antipsychotics with high anticholinergic burden were associated with an increased incidence of pneumonia. Significantly higher risks were detected for clozapine (≥180 mg/d), quetiapine (≥440 mg/d), and olanzapine (≥11 mg/d).

MeaningÌý Findings of this study suggest that in patients with schizophrenia, pneumonia is associated with the use of specific antipsychotics, setting the stage for personalized prevention strategies to decrease the incidence of this life-threatening condition in patients with schizophrenia.

Abstract

ImportanceÌý Antipsychotic drugs (particularly clozapine) have been associated with pneumonia in observational studies. Despite studies of the associations between antipsychotic use and incident pneumonia, it remains unclear to what degree antipsychotic use is associated with increased risk of pneumonia, whether dose-response associations exist, and what agents are specifically associated with incident pneumonia.

ObjectiveÌý To estimate pneumonia risk associated with specific antipsychotics and examine whether polytherapy, dosing, and receptor binding properties are associated with pneumonia in patients with schizophrenia.

Design, Setting, and ParticipantsÌý This cohort study identified patients with schizophrenia or schizoaffective disorder (hereafter, schizophrenia) aged 16 years or older from nationwide Finnish registers from 1972 to 2014. Data on diagnoses, inpatient care, and specialized outpatient care were obtained from the Hospital Discharge Register. Information on outpatient medication dispensing was obtained from the Prescription Register. Study follow-up was from 1996 to 2017. Data were analyzed from November 4, 2022, to December 5, 2023.

ExposuresÌý Use of specific antipsychotic monotherapies; antipsychotics modeled by dosage as low (<0.6 of the World Health Organization defined daily dose [DDD] per day), medium (0.6 to <1.1 DDDs per day), or high dose (≥1.1 DDDs per day); antipsychotic polypharmacy; and antipsychotics categorized according to their anticholinergic burden as low, medium, and high.

Main Outcomes and MeasuresÌý The primary outcome was hospitalization for incident pneumonia. Pneumonia risk was analyzed using adjusted, within-individual Cox proportional hazards regression models, with no antipsychotic use as the reference.

ResultsÌý The study included 61 889 persons with schizophrenia (mean [SD] age, 46.2 [16.0] years; 31 104 men [50.3%]). During 22 years of follow-up, 8917 patients (14.4%) had 1 or more hospitalizations for pneumonia and 1137 (12.8%) died within 30 days of admission. Compared with no antipsychotic use, any antipsychotic use overall was not associated with pneumonia (adjusted hazard ratio [AHR], 1.12; 95% CI, 0.99-1.26). Monotherapy use was associated with increased pneumonia risk compared with no antipsychotic use (AHR, 1.15 [95% CI, 1.02-1.30]; P = .03) in a dose-dependent manner, but polytherapy use was not. When categorized by anticholinergic burden, only the use of antipsychotics with a high anticholinergic burden was associated with pneumonia (AHR, 1.26 [95% CI, 1.10-1.45]; P < .001). Of specific drugs, high-dose quetiapine (AHR, 1.78 [95% CI, 1.22-2.60]; P = .003), high- and medium-dose clozapine (AHR, 1.44 [95% CI, 1.22-1.71]; P < .001 and AHR, 1.43 [95% CI, 1.18-1.74]; P < .001, respectively), and high-dose olanzapine (AHR, 1.29 [95% CI, 1.05-1.58]; P = .02) were associated with increased pneumonia risk.

Conclusions and RelevanceÌý Results of this cohort study suggest that in patients with schizophrenia, antipsychotic agents associated with pneumonia include not only clozapine (at dosages ≥180 mg/d) but also quetiapine (≥440 mg/d) and olanzapine (≥11 mg/d). Moreover, monotherapy antipsychotics and antipsychotics with high anticholinergic burden are associated with increased pneumonia risk in a dose-dependent manner. These findings call for prevention strategies aimed at patients with schizophrenia requiring high-risk antipsychotics.

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