Table 2. Clinical Outcomes Among 30 086 Children in the Retrospective Cohort.
No. (%) | Stratified Analysisa | Full Matched Analysisb | ||||
---|---|---|---|---|---|---|
Broad-Spectrum Antibiotics (n = 4296) |
Narrow-Spectrum Antibiotics (n = 25 790) |
Risk Difference (95% CI), %c |
P Value |
Risk Difference (95% CI), %c |
P Value |
|
Primary Outcomes at 14 d | ||||||
Treatment failured | 147 (3.4) | 809 (3.1) | 0 (−0.6 to 0.7) | .88 | 0.3 (−0.4 to 0.9) | .39 |
Adverse eventse | 157 (3.7) | 695 (2.7) | 0.9 (0.3 to 1.6) | .001 | 1.1 (0.4 to 1.8) | <.001 |
Secondary Outcomes at 30 d | ||||||
Treatment failured | 372 (8.7) | 2082 (8.1) | 0.3 (2.6 to 2.8) | .51 | 0.6 (−0.4 to 1.6) | .22 |
Adverse eventse | 189 (4.4) | 849 (3.3) | 1.1 (0.4 to 1.8) | .001 | 1.2 (0.5 to 1.9) | <.001 |
Comparisons were made within diagnosis and clinician strata. Risk differences were estimated using fixed-effects linear regression (first differencing method) and diagnosis and clinician strata were included as fixed effects.
Children prescribed narrow-spectrum antibiotics were optimally matched to children prescribed broad-spectrum antibiotics based on a propensity score estimated from patient-level and clinical-level characteristics creating matched sets of difference sizes using all children. Risk differences were estimated using weighted logistic regression with marginal standardization.
A risk difference of more than 0 means that broad-spectrum antibiotics had a higher risk of the adverse outcome than narrow-spectrum antibiotics.
Defined as having the same acute respiratory tract infection diagnosis during the in-person or telephone encounter and a new prescription for a systemic antibiotic.
Defined as encounters for diarrhea, vomiting, candidiasis, noncandidal rash, other or unspecified allergic reaction, and other or unspecified adverse event.