Cochrane · systematic review · CD003615
Oxcarbazepine versus phenytoin monotherapy for epilepsy: an individual participant data review
Nevitt, SJ, Tudur Smith, C, Marson, AG · Cochrane Database of Systematic Reviews · 2018 · Cochrane Library
SoF tableOnly the outcomes this review put in its Summary of Findings table are listed (the Cochrane Handbook caps them at about seven per comparison). Its other analyses are not shown here.
Questions
11
current version
GRADE rated
11
No studies
0
Included studies
NR
No studies 0 · 0%Ungraded 0 · 0%Very low 0 · 0%Low 2 · 18.2%Moderate 8 · 72.7%High 1 · 9.1%
Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.
Questions and results
Current version onlySummary of findings: oxcarbazepine versus phenytoin (primary outcomes)
Population: adults and children with newly diagnosed epilepsy
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Time to treatment failure (any reason related to treatment) All participants Range of Summary of findings: oxcarbazepine vs phenytoin (primary outcomes) | HR 0.78 [0.53, 1.14] | 2 studies · 476 participants | Moderate Downgraded: risk of bias, imprecision, indirectness |
Time to treatment failure (any reason related to treatment) Subgroup: focal onset seizures Range of Summary of findings: oxcarbazepine vs phenytoin (primary outcomes) | HR 0.69 [0.43, 1.09] | 2 studies · 333 participants | Moderate Downgraded: risk of bias, imprecision, indirectness |
Time to treatment failure (any reason related to treatment) Subgroup: generalised onset seizures Range of Summary of findings: oxcarbazepine vs phenytoin (primary outcomes) | HR 1.03 [0.51, 2.08] | 2 studies · 143 participants | Moderate Downgraded: risk of bias, imprecision, indirectness |
Time to treatment failure due to adverse events All participants Range of Summary of findings: oxcarbazepine vs phenytoin (primary outcomes) | HR 0.22 [0.1, 0.51] | 2 studies · 480 participants | High |
Time to treatment failure due to lack of efficacy All participants Range of Summary of findings: oxcarbazepine vs phenytoin (primary outcomes) | HR 1.17 [0.31, 4.35] | 2 studies · 480 participants | Moderate Downgraded: risk of bias, imprecision, indirectness |
Summary of findings: oxcarbazepine versus phenytoin (secondary outcomes)
Population: adults and children with newly diagnosed epilepsy
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Time to first seizure (post‐randomisation) All participants Range of Summary of findings: oxcarbazepine vs phenytoin (secondary outcomes) | HR 0.97 [0.75, 1.26] | 2 studies · 468 participants | Moderate Downgraded: risk of bias, indirectness |
Time to first seizure (post‐randomisation) Subgroup: focal onset seizures Range of Summary of findings: oxcarbazepine vs phenytoin (secondary outcomes) | HR 0.92 [0.68, 1.25] | 2 studies · 326 participants | Moderate Downgraded: risk of bias, indirectness |
Time to first seizure (post‐randomisation) Subgroup: generalised onset seizures Range of Summary of findings: oxcarbazepine vs phenytoin (secondary outcomes) | HR 1.11 [0.66, 1.86] | 2 studies · 142 participants | Low Downgraded: risk of bias, indirectness |
Time to achieve 12‐month remission (seizure‐free period) All participants Range of Summary of findings: oxcarbazepine vs phenytoin (secondary outcomes) | HR 1.04 [0.77, 1.41] | 2 studies · 468 participants | Moderate Downgraded: risk of bias, indirectness |
Time to achieve 12‐month remission (seizure‐free period) Subgroup: focal onset seizures Range of Summary of findings: oxcarbazepine vs phenytoin (secondary outcomes) | HR 1.09 [0.75, 1.57] | 2 studies · 326 participants | Moderate Downgraded: risk of bias, indirectness |
Time to achieve 12‐month remission (seizure‐free period) Subgroup: generalised onset seizures Range of Summary of findings: oxcarbazepine vs phenytoin (secondary outcomes) | HR 0.94 [0.55, 1.62] | 2 studies · 142 participants | Low Downgraded: risk of bias, indirectness |
Comparison
Population: adults and children with newly diagnosed epilepsy
| Outcome | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Time to withdrawal of allocated treatment ‐ all participants 8‐week titration period then 48‐week maintenance period Total: 56 weeks (392 days) | HR 1.64 [1.06, 2.54] | 2 studies · 476 participants | Moderate |
Time to withdrawal of allocated treatment Stratified by epilepsy type ‐ partial epilepsy 8‐week titration period then 48‐week maintenance period Total: 56 weeks (392 days) | HR 1.95 [1.15, 3.33] | 2 studies · 333 participants | Moderate |
Time to withdrawal of allocated treatment Stratified by epilepsy type ‐ generalised epilepsy 8‐week titration period then 48‐week maintenance period Total: 56 weeks (392 days) | HR 1.16 [0.54, 2.46] | 2 studies · 143 participants | Moderate |
Time to achieve 6‐month remission ‐ all participants 8‐week titration period then 48‐week maintenance period Total: 56 weeks (392 days) | HR 0.94 [0.74, 1.21] | 2 studies · 468 participants | Moderate |
Time to achieve 6‐month remission Stratified by epilepsy type ‐ partial epilepsy 8‐week titration period then 48‐week maintenance period Total: 56 weeks (392 days) | HR 0.85 [0.63, 1.15] | 2 studies · 326 participants | Moderate |
Time to achieve 6‐month remission Stratified by epilepsy type ‐ generalised epilepsy 8‐week titration period then 48‐week maintenance period Total: 56 weeks (392 days) | HR 1.2 [0.76, 1.89] | 2 studies · 142 participants | Moderate |
Time to achieve 12‐month remission ‐ all participants 8‐week titration period then 48‐week maintenance period Total: 56 weeks (392 days) | HR 0.95 [0.7, 1.29] | 2 studies · 468 participants | Moderate |
Time to achieve 12‐month remission Stratified by epilepsy type ‐ partial epilepsy 8‐week titration period then 48‐week maintenance period Total: 56 weeks (392 days) | HR 0.92 [0.64, 1.33] | 2 studies · 326 participants | Moderate |
Time to achieve 12‐month remission Stratified by epilepsy type ‐ generalised epilepsy 8‐week titration period then 48‐week maintenance period Total: 56 weeks (392 days) | HR 1.01 [0.59, 1.73] | 2 studies · 142 participants | Moderate |
Time to first seizure ‐ all participants 8‐week titration period then 48‐week maintenance period Total: 56 weeks (392 days) | HR 1.04 [0.8, 1.35] | 2 studies · 468 participants | Moderate |
Time to first seizure Stratified by epilepsy type ‐ partial epilepsy 8‐week titration period then 48‐week maintenance period Total: 56 weeks (392 days) | HR 1.08 [0.8, 1.47] | 2 studies · 326 participants | Moderate |
Time to first seizure Stratified by epilepsy type ‐ generalised epilepsy 8‐week titration period then 48‐week maintenance period Total: 56 weeks (392 days) | HR 0.94 [0.56, 1.56] | 2 studies · 142 participants | Moderate |