Journal
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
Volume 326, Issue 15, Pages 1504-1515Publisher
AMER MEDICAL ASSOC
DOI: 10.1001/jama.2021.15255
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In this study, new prescription dispensation of tramadol was significantly associated with a higher risk of all-cause mortality, cardiovascular events, and fractures compared to codeine, with no significant differences in the risk of other adverse outcomes. The findings emphasize the importance of cautious interpretation due to potential residual confounding.
Question Is tramadol compared with codeine prescription dispensation associated with differences in the risk of mortality and other clinical outcomes? Findings In this retrospective cohort study that used propensity score matching and included 368 960 participants, a new prescription dispensation of tramadol, compared with codeine, was significantly associated with a higher risk of all-cause mortality (HR, 2.31), cardiovascular events (HR, 1.15), and fractures (HR, 1.50), but there was no significant difference in the risk of constipation, delirium, falls, opioid abuse/dependence, or sleep disorders. Meaning New prescription dispensation of tramadol, compared with codeine, was significantly associated with a higher risk of mortality, cardiovascular events, and fractures, although the findings should be interpreted cautiously, given the potential for residual confounding. Importance Although tramadol is increasingly used to manage chronic noncancer pain, few safety studies have compared it with other opioids. Objective To assess the associations of tramadol, compared with codeine, with mortality and other adverse clinical outcomes as used in outpatient settings. Design, Setting, and Participants Retrospective, population-based, propensity score-matched cohort study using a primary care database with routinely collected medical records and pharmacy dispensations covering more than 80% of the population of Catalonia, Spain (approximate to 6 million people). Patients 18 years or older with 1 or more year of available data and dispensation of tramadol or codeine (2007-2017) were included and followed up to December 31, 2017. Exposures New prescription dispensation of tramadol or codeine (no dispensation in the previous year). Main Outcomes and Measures Outcomes studied were all-cause mortality, cardiovascular events, fractures, constipation, delirium, falls, opioid abuse/dependence, and sleep disorders within 1 year after the first dispensation. Absolute rate differences (ARDs) and hazard ratios (HRs) with 95% confidence intervals were calculated using cause-specific Cox models. Results Of the 1 093 064 patients with a tramadol or codeine dispensation during the study period (326 921 for tramadol, 762 492 for codeine, 3651 for both drugs concomitantly), a total of 368 960 patients (184 480 propensity score-matched pairs) were included after study exclusions and propensity score matching (mean age, 53.1 [SD, 16.1] years; 57.3% women). Compared with codeine, tramadol dispensation was significantly associated with a higher risk of all-cause mortality (incidence, 13.00 vs 5.61 per 1000 person-years; HR, 2.31 [95% CI, 2.08-2.56]; ARD, 7.37 [95% CI, 6.09-8.78] per 1000 person-years), cardiovascular events (incidence, 10.03 vs 8.67 per 1000 person-years; HR, 1.15 [95% CI, 1.05-1.27]; ARD, 1.36 [95% CI, 0.45-2.36] per 1000 person-years), and fractures (incidence, 12.26 vs 8.13 per 1000 person-years; HR, 1.50 [95% CI, 1.37-1.65]; ARD, 4.10 [95% CI, 3.02-5.29] per 1000 person-years). No significant difference was observed for the risk of falls, delirium, constipation, opioid abuse/dependence, or sleep disorders. Conclusions and Relevance In this population-based cohort study, a new prescription dispensation of tramadol, compared with codeine, was significantly associated with a higher risk of subsequent all-cause mortality, cardiovascular events, and fractures, but there was no significant difference in the risk of constipation, delirium, falls, opioid abuse/dependence, or sleep disorders. The findings should be interpreted cautiously, given the potential for residual confounding. This propensity score-matched cohort study uses primary care data to assess the associations of tramadol, compared with codeine, with all-cause mortality and other adverse clinical outcomes (cardiovascular events, fractures, constipation, delirium, falls, opioid abuse/dependence, and sleep disorders) 1 year after first dispensation in outpatient settings in Catalonia, Spain.
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