17. Relapse/Return to the emergency department.
Intervention/Comparison | Outcome | Illustrative comparative risks (95% CI) | Relative effect: risk ratio (95% CI) | Number of participants (studies) | Certaintyof the evidence (GRADE) | Comments: overview authors' assessment of the certainty of evidence | |
Assumed risk | Corresponding risk | ||||||
With comparator | With intervention | ||||||
Anticholinergic and SABA vs SABA alone (Griffiths 2013) | Relapse | 45 per 1000 | 48 per 1000 (31 to 76) | 1.07 (0.68 to 1.68) | 1389 (10) | Low | Certainty downgraded due to serious imprecision and risk of bias in review (single author selected possible citations) |
Oral LTRA vs control (Watts 2012) | Relapse within 7 days | 83 per 1000 | 32 per 1000 (1 to 727) | 0.39 (0.02 to 8.73) | 22 (1) | Low | Certainty downgraded due to very serious imprecision |
Inhaled anticholinergics + SABA vs SABA alone for children hospitalised with asthma (Vezina 2014) | Relapse within 72 hours of discharge from hospital | 0 per 1000 | 0 (not estimable) | Not estimable | 80 (1) | Low | Certainty downgraded due to risk of bias in review (single author selected possible citations) and serious imprecision |
IV magnesium sulfate (Griffiths 2016) | Return to ED within 48 hours | 22 per 1000 | 9 per 1000 (1 to 211) | 0.41 (0.02 to 9.71) | 85 (2) | Low | Certainty downgraded due to very serious imprecision |
CI: confidence interval; ED: emergency department; GRADE: Grading of Recommendations Assessment, Development and Evaluation; LTRA: leukotriene receptor antagonist; SABA: short acting beta2‐agonist.