Serum creatine phosphokinase elevation in patients treated with intravenous magnesium sulfate

Objective: During the treatment of pre-term labor with magnesium sulfate, we noted an abnormal elevation of maternal serum creatine phosphokinase. This study was aimed at evaluating the relationship between tocolysis with MgSO 4 and maternal serum CPK elevation, which represents the possible damage...

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Published in:International journal of gynecology and obstetrics Vol. 76; no. 3; pp. 257 - 266
Main Authors: Kuno, N, Ishikawa, K
Format: Journal Article
Language:English
Published: Shannon Elsevier Ireland Ltd 01-03-2002
Elsevier Science
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Abstract Objective: During the treatment of pre-term labor with magnesium sulfate, we noted an abnormal elevation of maternal serum creatine phosphokinase. This study was aimed at evaluating the relationship between tocolysis with MgSO 4 and maternal serum CPK elevation, which represents the possible damage of muscles by magnesium sulfate. Methods: Clinical records of 45 women treated with magnesium sulfate and beta-sympathomimetics for the treatment of pre-term labor were retrospectively examined. Results: Serum CPK was abnormally elevated in 32 out of 45 cases (71.1%), but in only one out of 21 in the control group. In three cases, the decrease of serum creatine phosphokinase after cessation of magnesium sulfate was demonstrated, despite the continuous infusion of beta-sympathomimetics. Conclusions: Magnesium sulfate may cause muscular damage and abnormal elevation of maternal serum creatine phosphokinase. Special attention must be paid to patients when drugs acting on muscle cells, for example succinyl choline, are going to be used.
AbstractList Objective: During the treatment of pre-term labor with magnesium sulfate, we noted an abnormal elevation of maternal serum creatine phosphokinase. This study was aimed at evaluating the relationship between tocolysis with MgSO 4 and maternal serum CPK elevation, which represents the possible damage of muscles by magnesium sulfate. Methods: Clinical records of 45 women treated with magnesium sulfate and beta-sympathomimetics for the treatment of pre-term labor were retrospectively examined. Results: Serum CPK was abnormally elevated in 32 out of 45 cases (71.1%), but in only one out of 21 in the control group. In three cases, the decrease of serum creatine phosphokinase after cessation of magnesium sulfate was demonstrated, despite the continuous infusion of beta-sympathomimetics. Conclusions: Magnesium sulfate may cause muscular damage and abnormal elevation of maternal serum creatine phosphokinase. Special attention must be paid to patients when drugs acting on muscle cells, for example succinyl choline, are going to be used.
Objective: During the treatment of pre‐term labor with magnesium sulfate, we noted an abnormal elevation of maternal serum creatine phosphokinase. This study was aimed at evaluating the relationship between tocolysis with MgSO4 and maternal serum CPK elevation, which represents the possible damage of muscles by magnesium sulfate. Methods: Clinical records of 45 women treated with magnesium sulfate and beta‐sympathomimetics for the treatment of pre‐term labor were retrospectively examined. Results: Serum CPK was abnormally elevated in 32 out of 45 cases (71.1%), but in only one out of 21 in the control group. In three cases, the decrease of serum creatine phosphokinase after cessation of magnesium sulfate was demonstrated, despite the continuous infusion of beta‐sympathomimetics. Conclusions: Magnesium sulfate may cause muscular damage and abnormal elevation of maternal serum creatine phosphokinase. Special attention must be paid to patients when drugs acting on muscle cells, for example succinyl choline, are going to be used.
During the treatment of pre-term labor with magnesium sulfate, we noted an abnormal elevation of maternal serum creatine phosphokinase. This study was aimed at evaluating the relationship between tocolysis with MgSO4 and maternal serum CPK elevation, which represents the possible damage of muscles by magnesium sulfate. Clinical records of 45 women treated with magnesium sulfate and beta-sympathomimetics for the treatment of pre-term labor were retrospectively examined. Serum CPK was abnormally elevated in 32 out of 45 cases (71.1%), but in only one out of 21 in the control group. In three cases, the decrease of serum creatine phosphokinase after cessation of magnesium sulfate was demonstrated, despite the continuous infusion of beta-sympathomimetics. Magnesium sulfate may cause muscular damage and abnormal elevation of maternal serum creatine phosphokinase. Special attention must be paid to patients when drugs acting on muscle cells, for example succinyl choline, are going to be used.
Author Kuno, N
Ishikawa, K
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  surname: Ishikawa
  fullname: Ishikawa, K
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Issue 3
Keywords Tocolysis
Magnesium
CPK
Human
Magnesium sulfate
Treatment
Intravenous administration
Pregnancy disorders
Enzyme
Creatine kinase
Transferases
Female
Threatened premature delivery
Tocolytic
Language English
License CC BY 4.0
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Elsevier Science
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Snippet Objective: During the treatment of pre-term labor with magnesium sulfate, we noted an abnormal elevation of maternal serum creatine phosphokinase. This study...
Objective: During the treatment of pre‐term labor with magnesium sulfate, we noted an abnormal elevation of maternal serum creatine phosphokinase. This study...
During the treatment of pre-term labor with magnesium sulfate, we noted an abnormal elevation of maternal serum creatine phosphokinase. This study was aimed at...
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pascalfrancis
wiley
elsevier
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StartPage 257
SubjectTerms Biological and medical sciences
CPK
Creatine Kinase - blood
Female
Genital system. Reproduction
Humans
Magnesium
Magnesium Sulfate - adverse effects
Magnesium Sulfate - therapeutic use
Medical sciences
Obstetric Labor, Premature
Pharmacology. Drug treatments
Pregnancy
Retrospective Studies
Sympathomimetics - therapeutic use
Tocolysis
Tocolytic Agents - adverse effects
Tocolytic Agents - therapeutic use
Title Serum creatine phosphokinase elevation in patients treated with intravenous magnesium sulfate
URI https://dx.doi.org/10.1016/S0020-7292(01)00582-3
https://onlinelibrary.wiley.com/doi/abs/10.1016%2FS0020-7292%2801%2900582-3
https://www.ncbi.nlm.nih.gov/pubmed/11880128
Volume 76
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