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. Author manuscript; available in PMC: 2014 Dec 17.
Published in final edited form as: Cochrane Database Syst Rev. 2013 Dec 3;12:CD005431. doi: 10.1002/14651858.CD005431.pub3
Outcome or subgroup title No. of studies No. of participants Statistical method Effect size
1 Unspecified time for visual acuity between 20/20 and 20/40 1 Odds Ratio (M-H, Fixed, 95% CI) Totals not selected
2 Time to resolution of primary hemorrhage (days) 1 Mean Difference (IV, Fixed, 95% CI) Totals not selected
3 Risk of secondary hemorrhage 1 Odds Ratio (M-H, Fixed, 95% CI) Totals not selected
4 Time to rebleed (days) Other data No numeric data
5 Risk of glaucoma or elevated intraocular pressure (IOP) 1 Odds Ratio (M-H, Fixed, 95% CI) Totals not selected
6 Adverse effects 1 Odds Ratio (M-H, Fixed, 95% CI) Totals not selected
 6.1 Nausea or vomiting 1 Odds Ratio (M-H, Fixed, 95% CI) 0.0 [0.0, 0.0]
 6.2 Dizziness or hypotension 1 Odds Ratio (M-H, Fixed, 95% CI) 0.0 [0.0, 0.0]
 6.3 Syncope 1 Odds Ratio (M-H, Fixed, 95% CI) 0.0 [0.0, 0.0]
 6.4 Diarrhea 1 Odds Ratio (M-H, Fixed, 95% CI) 0.0 [0.0, 0.0]
 6.5 Rash or pruritis 1 Odds Ratio (M-H, Fixed, 95% CI) 0.0 [0.0, 0.0]
 6.6 Hot flashes 1 Odds Ratio (M-H, Fixed, 95% CI) 0.0 [0.0, 0.0]
 6.7 Dry mouth or nose 1 Odds Ratio (M-H, Fixed, 95% CI) 0.0 [0.0, 0.0]
7 Duration of hospitalization (days) 1 Mean Difference (IV, Fixed, 95% CI) Totals not selected