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Treatment of children with infantile spasms: A network meta-analysis
Puneet Jain1, Jitendra K Sahu2, Paul S Horn3,4
1Epilepsy Program, Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Insights
High-dose adrenocorticotropic hormone (ACTH) and prednisolone are most effective for infantile spasms. These treatments show superior remission rates compared to other non-surgical interventions for this condition.
Area of Science:
- Pediatric Neurology
- Pharmacology
- Clinical Trials
Background:
- Infantile spasms are a rare and severe epilepsy syndrome in infants.
- Early diagnosis and treatment are crucial for improving outcomes.
- Non-surgical interventions are the mainstay of treatment, but comparative effectiveness data are limited.
Purpose of the Study:
- To systematically review and perform a network meta-analysis (NMA) of non-surgical interventions for infantile spasms.
- To provide comparative effectiveness estimates and rankings for first-line treatments.
- To identify the most effective interventions for achieving remission.
Main Methods:
- Systematic review and network meta-analysis (NMA) of randomized controlled trials (RCTs).
- Included RCTs involved children aged 2 months to 3 years with infantile spasms.
- Analyzed electroclinical and clinical remission rates within one month of treatment initiation.
Main Results:
- Seventeen RCTs were included in the NMA, comparing various first-line treatments.
- For electroclinical remission, high-dose ACTH, methylprednisolone, low-dose ACTH/MgSO4, low-dose ACTH, and high-dose prednisolone were ranked highest.
- For clinical remission, low-dose ACTH/MgSO4, high-dose ACTH, high-dose prednisolone, and low-dose ACTH were ranked highest.
Conclusions:
- Adrenocorticotropic hormone (ACTH) and high-dose prednisolone are more effective in achieving both electroclinical and clinical remissions for infantile spasms.
- These treatments demonstrate superior efficacy compared to other non-surgical options.
- Symptomatic etiology negatively impacts remission likelihood, even when accounting for treatment lag.
Aim:
We performed a systematic review and network meta-analysis (NMA) to obtain comparative effectiveness estimates and rankings of non-surgical interventions used to treat infantile spasms.
Method:
All randomized controlled trials (RCTs) including children 2 months to 3 years of age with infantile spasms (with hypsarrhythmia or hypsarrhythmia variants on electroencephalography) receiving appropriate first-line medical treatment were included. Electroclinical and clinical remissions within 1 month of starting treatment were analyzed.
Results:
Twenty-two RCTs comparing first-line treatments for infantile spasms were reviewed; of these, 17 were included in the NMA. Both frequentist and Bayesian network rankings for electroclinical remission showed that high dose adrenocorticotropic hormone (ACTH), methylprednisolone, low dose ACTH and magnesium sulfate (MgSO4 ) combination, low dose ACTH, and high dose prednisolone were most likely to be the 'best' interventions, although these were not significantly different from each other. For clinical remission, low dose ACTH/MgSO4 combination, high dose ACTH (with/without vitamin B6 ), high dose prednisolone, and low dose ACTH were 'best'.
Interpretation:
Treatments including ACTH and high dose prednisolone are more effective in achieving electroclinical and clinical remissions for infantile spasms.
What This Paper Adds:
Adrenocorticotropic hormone and high dose prednisolone are more effective than other medications for infantile spasms. Symptomatic etiology decreases the likelihood of remission even after adjusting for treatment lag.
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