Dose optimization of intravenous magnesium sulfate after acute stroke

Parenterally administered MgSO4 is neuroprotective in standard animal models of focal cerebral ischemia and in many other paradigms of brain injury. Previous small clinical trials in stroke patients have explored the safety and tolerability of different infusion regimens. This study was undertaken t...

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Veröffentlicht in:Stroke (1970) 1998-05, Vol.29 (5), p.918-923
Hauptverfasser: MUIR, K. W, LEES, K. R
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LEES, K. R
description Parenterally administered MgSO4 is neuroprotective in standard animal models of focal cerebral ischemia and in many other paradigms of brain injury. Previous small clinical trials in stroke patients have explored the safety and tolerability of different infusion regimens. This study was undertaken to optimize the regimen for a multicenter trial. Within 24 hours of the onset of clinically diagnosed stroke, patients were randomized to receive placebo or one of three intravenous MgSO4 infusions: a loading infusion of 8, 12, or 16 mmol, followed by 65 mmol over 24 hours. Cardiovascular parameters, serum magnesium concentrations, and blood glucose concentrations were determined. Outcome at 30 and 90 days was recorded. Twenty-five patients were recruited and treated at a mean time of 20 hours after stroke. No tolerability problems were identified. No effects of magnesium on heart rate, blood pressure, or blood glucose were evident. Serum magnesium concentrations rose to target levels most rapidly in the highest loading infusion group and were maintained in all groups for at least 24 hours. MgSO4 infusions that rapidly elevate the serum magnesium concentration to potentially therapeutic levels are well tolerated and have no major hemodynamic effects in patients with acute stroke. The 16-mmol loading infusion achieved target serum concentrations most rapidly and has been chosen for further trials.
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W ; LEES, K. R</creator><creatorcontrib>MUIR, K. W ; LEES, K. R</creatorcontrib><description>Parenterally administered MgSO4 is neuroprotective in standard animal models of focal cerebral ischemia and in many other paradigms of brain injury. Previous small clinical trials in stroke patients have explored the safety and tolerability of different infusion regimens. This study was undertaken to optimize the regimen for a multicenter trial. Within 24 hours of the onset of clinically diagnosed stroke, patients were randomized to receive placebo or one of three intravenous MgSO4 infusions: a loading infusion of 8, 12, or 16 mmol, followed by 65 mmol over 24 hours. Cardiovascular parameters, serum magnesium concentrations, and blood glucose concentrations were determined. Outcome at 30 and 90 days was recorded. Twenty-five patients were recruited and treated at a mean time of 20 hours after stroke. No tolerability problems were identified. No effects of magnesium on heart rate, blood pressure, or blood glucose were evident. Serum magnesium concentrations rose to target levels most rapidly in the highest loading infusion group and were maintained in all groups for at least 24 hours. MgSO4 infusions that rapidly elevate the serum magnesium concentration to potentially therapeutic levels are well tolerated and have no major hemodynamic effects in patients with acute stroke. 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R</creatorcontrib><title>Dose optimization of intravenous magnesium sulfate after acute stroke</title><title>Stroke (1970)</title><addtitle>Stroke</addtitle><description>Parenterally administered MgSO4 is neuroprotective in standard animal models of focal cerebral ischemia and in many other paradigms of brain injury. Previous small clinical trials in stroke patients have explored the safety and tolerability of different infusion regimens. This study was undertaken to optimize the regimen for a multicenter trial. Within 24 hours of the onset of clinically diagnosed stroke, patients were randomized to receive placebo or one of three intravenous MgSO4 infusions: a loading infusion of 8, 12, or 16 mmol, followed by 65 mmol over 24 hours. Cardiovascular parameters, serum magnesium concentrations, and blood glucose concentrations were determined. Outcome at 30 and 90 days was recorded. Twenty-five patients were recruited and treated at a mean time of 20 hours after stroke. 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Drug treatments</topic><topic>Systole</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MUIR, K. W</creatorcontrib><creatorcontrib>LEES, K. R</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Stroke (1970)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MUIR, K. W</au><au>LEES, K. 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The 16-mmol loading infusion achieved target serum concentrations most rapidly and has been chosen for further trials.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins</pub><pmid>9596235</pmid><doi>10.1161/01.STR.29.5.918</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; American Heart Association Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection; Journals@Ovid Complete
subjects Acute Disease
Aged
Anticonvulsants - administration & dosage
Anticonvulsants - therapeutic use
Biological and medical sciences
Blood Glucose - drug effects
Blood Glucose - metabolism
Blood Pressure - drug effects
Blood Pressure - physiology
Cerebral Hemorrhage - drug therapy
Cerebral Infarction - drug therapy
Cerebrovascular Disorders - blood
Cerebrovascular Disorders - drug therapy
Diastole
Double-Blind Method
Female
Heart Rate - drug effects
Heart Rate - physiology
Humans
Hypotension - etiology
Injections, Intravenous
Magnesium - blood
Magnesium Sulfate - administration & dosage
Magnesium Sulfate - therapeutic use
Male
Medical sciences
Neuropharmacology
Neuroprotective agent
Pharmacology. Drug treatments
Systole
Time Factors
Treatment Outcome
title Dose optimization of intravenous magnesium sulfate after acute stroke
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