Table 4.
Incidence rate ratios for adverse events associated with short term use of oral corticosteroids, by reason for medical visit
Adverse event | 5-30 days* | P value | 31-90 days* | P value | |
---|---|---|---|---|---|
Incidence rate ratio† (95% CI) | Incidence rate ratio† (95% CI) | ||||
Sepsis: | |||||
Respiratory conditions‡ | 3.77 (1.94 to 7.35) | <0.001 | 2.53 (1.25 to 5.10) | 0.01 | |
Musculoskeletal conditions§ | 12.91 (5.49 to 30.34) | <0.001 | 4.32 (1.87 to 9.97) | 0.001 | |
Venous thromboembolism: | |||||
Respiratory conditions‡ | 3.11 (2.20 to 4.40) | <0.001 | 1.27 (0.88 to 1.82) | 0.20 | |
Musculoskeletal conditions§ | 4.70 (3.08 to 7.17) | <0.001 | 2.02 (1.31 to 3.11) | 0.001 | |
Fracture: | |||||
Respiratory conditions‡ | 1.96 (1.63 to 2.37) | <0.001 | 1.33 (1.13 to 1.56) | <0.001 | |
Musculoskeletal conditions§ | 2.46 (2.02 to 3.00) | <0.001 | 1.65 (1.37 to 1.99) | <0.001 |
*Number of days from date when corticosteroid prescription was filled. Reference period was 5-180 days before prescription date.
†Sepsis was adjusted for antibiotics, 5-HT3 receptor antagonists, antidepressants, anti-inflammatory agents, antimuscarinics, opiate agonists, and phenothiazine. Venous thromboembolism was adjusted for antibiotics, androgens, anxiolytics, anti-inflammatory agents, azoles, calcium channel blockers, coumarin, diuretics, opiate agonists, and platelet aggregation inhibitors. Fractures were adjusted for anti-inflammatory agents, COX-2 inhibitors, and opiate agonists.
‡Upper respiratory tract infection, allergy, bronchitis, lower respiratory tract disorder, upper respiratory tract disorder, or asthma.
§Spinal conditions, connective tissue disorders, or joint disorders.