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[Preprint]. 2020 Nov 25:2020.07.14.20152728. [Version 3] doi: 10.1101/2020.07.14.20152728

Table 3: Placebo-controlled studies:

Secondary outcomes

Variables No of trials Proportion with ≥1 event, intervention group (%) Proportion with ≥1 event, control group (%) Odds ratio (95% CI) I2 % P for heterogeneity
Efficacy outcomes
Upper respiratory infection* 28 7931/13493 (58.8) 7823/13034 (60.0) 0.96 (0.90 to 1.02) 4.4 0.40
Lower respiratory infection* 14 3583/12167 (29.4) 3601/12027 (29.9) 0.98 (0.93 to 1.04) 0.0 0.56
Emergency department attendance and/or hospital admission due to ARI 18 117/9887 (1.2) 125/9769 (1.3) 0.90 (0.70 to 1.16) 0.0 1.00
Death due to ARI or respiratory failure 33 14/13612 (0.1) 11/13058 (0.1) 1.04 (0.61 to 1.78) 0.0 1.00
Use of antibiotics to treat an ARI* 13 2035/7562 (26.9) 2082/7423 (28.0) 0.91 (0.82 to 1.02) 13.4 0.31
Absence from work or school due to ARI 10 378/1527 (24.7) 364/1044 (34.9) 0.91 (0.69 to 1.20) 35.3 0.13
Safety outcomes
Serious adverse event of any cause* 35 545/13861 (3.9) 554/13326 (4.2) 0.97 (0.86 to 1.09) 0.0 1.00
Death due to any cause 34 117/13854 (0.8) 97/13293 (0.7) 1.15 (0.90 to 1.49) 0.0 1.00
Hypercalcaemia 21 50/9294 (0.5) 39/8919 (0.4) 1.20 (0.81 to 1.79) 0.0 1.00
Renal stones 20 110/11540 (1.0) 128/11138 (1.1) 0.85 (0.66 to 1.10) 0.0 1.00
*

This analysis includes a subset of participants in the trial by Pham et al, who completed symptom diaries.