REVIEW ARTICLEAntipsychotic drug exposure and risk of fracture a systematic review and meta-analysis of observational studiesPapola, Davidea,b; Ostuzzi, Giovannia; Thabane, Lehanab; Guyatt, Gordonb; Barbui, Corradoa Author Information aDepartment of Neuroscience, Biomedicine and Movement Science, WHO Collaborating Centre for Research and Training in Mental Health and Service Evaluation, Section of Psychiatry, University of Verona, Verona, Italy bDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada Correspondence to Davide Papola, MD, Department of Neuroscience, Biomedicine and Movement Sciences, WHO Collaborating Centre for Research and Training in Mental Health and Service Evaluation, Section of Psychiatry, University of Verona, Piazzale Scuro 10, 37134 Verona, Italy Tel: +39 045 812 4063; fax: +39 045 802 7498; e-mail: [email protected] Received February 13, 2018 Accepted April 5, 2018 International Clinical Psychopharmacology 33(4):p 181-196, July 2018. | DOI: 10.1097/YIC.0000000000000221 Buy SDC Metrics Abstract To investigate the extent to which exposure to first-generation and second-generation antipsychotics (APs) is associated with an increased risk of fractures, with a particular focus on hip fractures, and to ascertain the risk associated with exposure to individual drugs. We included observational studies that reported data on fractures in individuals exposed to APs compared with unexposed individuals or individuals with previous exposure. We extracted information on study design, source of data, population characteristics, outcomes of interest, matching and confounding factors, and used a modified version of the Newcastle–Ottawa Scale to judge study risk of bias. We pooled adjusted estimates of relative effects to generate pooled odds ratios (ORs) and their 95% confidence interval (CI) using a random-effects model. We rated the quality of evidence using the GRADE approach. Of 36 observational studies, 29 proved to have a low risk of bias and seven were found to have a high risk of bias. The risk of hip fracture (OR: 1.57, 95% CI: 1.42–1.74, low quality of evidence) and of any fracture (OR: 1.17, 95% CI: 1.04–1.31, very low quality of evidence) increased with exposure to APs, with similar increases in risk in the first generation and second generation. The risk was similar among different diagnostic categories. The few studies that provided data were insufficient to allow inferences on individual drugs. AP exposure in unselected populations was associated with a 57% increase in the risk of hip fractures and a 17% increase in the risk of any fractures. Between-study heterogeneity limits the confidence in this estimate. Copyright © 2018 Wolters Kluwer Health, Inc. All rights reserved.