16 mMol bolus of MgSO4followed by 8 mMol/hour continuous infusion for 10 days
55/55
(i) Lower incidence of CVS in Mg2+ group (ii) Lower incidence of delayed ischemic infarction in Mg2+ group (iii) DIND nonsignificantly reduced in Mg2+ group, though fewer patients with DIND expressed delayed ischemic infarction
15 mMol/L MgSO4 at 20 mL/hour (intracisternal) for 20 days
10
(i) Five patients had good recovery (ii) One patient exhibited moderate disability (iii) One patient exhibited severe disability (iv) Two patients progressed to a vegetative state (v) One patient died
(i) Risk of DCI was lower in patients with higher serum magnesium concentrations when compared to the lowest quartile (ii) No effect on incidence of poor outcome
10 mg/kg bolus followed by 30 mg/kg (IV) infusion of MgSO4 for 7 days
53/51
(i) No difference in outcome measured by GOS after 12 months (ii) Similar incidence of CVS in both groups (iii) Rate of cerebral infarction similar in both groups.
20 mMol bolus followed by 80 mMol/day (IV) for 14 days
30/30
(i) CVS incidence decreased, but not statistically significant (ii) Vasospasm detected via TCD shorter in duration (iii) No difference in outcome measured by GOS at 6 months
20 mMol bolus of MgSO4followed by 120–150 mMol/day
48 treated with nimodipine, Triple-H therapy, bed rest/ 24 treated with MgSO4 adjunct
(i) Incidence of vasospasm was reported to be equal in both groups. (ii) Vasospasm occurring in the nimodipine-only group was correlated with longer hospital stays, when compared to the MgSO4 adjunct group
(i) No adverse effects from continuous magnesium infusion (ii) Lower incidence of both angiographic and clinical CVS observed than the literature values
(i) No benefit from magnesium infusion on the incidence of cerebral infarction (ii) Nonsignificant increase for odds ratio of favorable outcome at 3 and 6 months.
(i) Magnesium infusion reduced the risk for DCI and poor outcome after SAH (ii) Serum levels need to be monitored closely to prevent adverse side effects