Introduction: The aim of this prospective audit was to assess the effectiveness and safety of rectal paraldehyde in the management of acute, including prolonged, tonic–clonic convulsions. There are very limited published data on its effectiveness and safety, and previous data have focused on its intramuscular route of administration.
Methods: Four hospitals participated in the study. Information was collected on each dose of paraldehyde used for the treatment of a tonic–clonic convulsion over 1 year. Data were not included on patients treated with rectal paraldehyde for other seizure types or non-convulsive status epilepticus.
Results: Data analysis was undertaken regarding 53 episodes in 30 patients. Patient’s ages ranged from 5 months to 16 years (mean 6.12 years, median 5.91 years). A pre-existing diagnosis of epilepsy was recorded in 35 episodes (66%). The mean dose of paraldehyde was 0.65 ml/kg (SD 0.22, 95% CI 0.59 to 0.71) and median dose 0.79 ml/kg. Rectal paraldehyde terminated the convulsion in 33 (62.3%) of the 53 episodes. In the 35 episodes where a pre-existing diagnosis of epilepsy was recorded, paraldehyde stopped the convulsion on 26 (74.3%) occasions. There was no difference in the dose of paraldehyde between the episodes where the convulsion was or was not terminated. There was no recorded respiratory depression in any episode.
Conclusions: This study provides unique evidence that rectal paraldehyde is effective and safe in treating acute prolonged tonic–clonic convulsions. This would appear to confirm that paraldehyde should remain a treatment for the management of prolonged tonic–clonic convulsions, including convulsive status epilepticus.
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Competing interests None.
Contributors: REA, AG and ABS were responsible for the original study idea and design. AGR analysed the data. REA is a member of the original and current Status Epilepticus Working Group.
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