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A Metin Gülmezoglu National Perinatal Epidemiology Unit,
Radcliffe Infirmary, Oxford OX2 6HE
Correspondence to: Dr A M Gülmezoglu, United
Kingdom Cochrane Centre, NHS Research and Development Programme,
Summertown Pavilion, Oxford OX2 7LG mgulmezoglu{at}cochrane.co.uk
Pre-eclampsia is a multisystem disorder associated with
hypertension and proteinuria and is a fairly common complication of pregnancy. Eclampsia, the occurrence of fits with pre-eclampsia, is
rare, but both conditions can have serious consequences for the mother
and infant. Anticonvulsants are given to women with eclampsia to
prevent further fits and to women with pre-eclampsia to prevent the
first fit, thereby improving the outcome for mother and infant.
Clinical practice, however, varies greatly worldwide. In the United
Kingdom diazepam has been popular since the 1970s and phenytoin
since the early 1990s, but the use of magnesium sulphate remains
uncommon.
1 2
Magnesium sulphate has been widely used for
decades in the United States and has recently been acknowledged as the
preferred anticonvulsant for women with eclampsia.3 There
is little evidence to support or refute the use of anticonvulsants in
women with pre-eclampsia.4 We conducted a survey to
determine the current use of anticonvulsants in eclampsia and
pre-eclampsia.
A questionnaire was sent to consultants in the United Kingdom and
the Republic of Ireland asking about their use of anticonvulsants in
women with eclampsia or pre-eclampsia. Two reminders were sent six
weeks apart.
The table summarises the main results. Of the 662 respondents who used
prophylactic anticonvulsants, 658 were more likely to prescribe them in
the presence of signs or symptoms of imminent eclampsia and 364 would
consider using an anticonvulsant if delivery was unlikely within the
next 24 hours. Over half (475) of the respondents would collaborate in
a placebo controlled trial of magnesium sulphate versus placebo in
women with pre-eclampsia.
Compared with earlier surveys,
1 2
our survey
was shorter and simpler and focused largely on anticonvulsant use. Our
survey also had a slightly better response rate (table). Since 1991, when the last survey was conducted,2 the reported use of
magnesium sulphate in pre-eclampsia has risen from 2% to 40%. During
1992 only 2% of women with eclampsia received magnesium
sulphate,5 whereas 60% of respondents in our survey said
that they would now use this anticonvulsant for such women. As the use
of magnesium sulphate had remained at 2% for 14 years,2
this change probably occurred after publication of evidence showing
that magnesium sulphate is better than diazepam or phenytoin for
eclampsia.3 Despite this substantial shift in practice,
diazepam remains the most widely used anticonvulsant for pre-eclampsia
and eclampsia, and phenytoin continues to be used by a quarter of
respondents. We believe that magnesium sulphate should be used in
preference to diazepam and phenytoin.
Uncertainty about the role and choice of prophylactic anticonvulsant
treatment for pre-eclampsia is reflected in the variation in clinical
practice. For example, an increasing proportion of obstetricians never
use prophylactic anticonvulsants (16% in 1991 v 23% in
1996).2 Among those who do there is no consensus on which
agent to use or when prophylaxis is appropriate (data not shown). One
aim of our survey was to assess the feasibility of conducting a
multicentre, randomised, placebo controlled trial of magnesium sulphate
versus placebo in women with pre-eclampsia. Over half of the
respondents indicated their interest in collaborating in such a study
compared with only 3% of respondents in the 1991 survey.2
This confirms the increased uncertainty about the role of
anticonvulsants in women with pre-eclampsia.
We thank the respondents to our questionnaire.
Contributors: LD had the original idea and participated in the
design and conduct of the study. AMG participated in the design and
conduct of the study and was responsible for coordination. Both authors
supervised the analysis and wrote the paper and will act as guarantors
for the paper. Sarah Ayers provided programming support and Caroline
Busby entered the data.
Funding: This study was funded by a grant from the Department
for International Development; it does not take any responsibility for
the contents of this article.
Conflict of interest: None.
(Accepted 5 August 1997)
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Subjects, methods, and results
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Comment
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Acknowledgments
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References
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References
© BMJ 1998