Table 1.
Important outcomes | Seizure frequency, quality of life, adverse effects | ||||||||
Number of studies (participants) | Outcome | Comparison | Type of evidence | Quality | Consistency | Directness | Effect size | GRADE | Comment |
What are the effects of monotherapy in newly diagnosed generalised epilepsy (tonic clonic type)? | |||||||||
4 (395) | Seizure frequency | Carbamazepine v sodium valproate | 4 | −1 | 0 | −1 | 0 | Low | Quality point deducted for subgroup analysis. Directness point deducted for uncertainty about epilepsy classification |
4 (157) | Seizure frequency | Carbamazepine v phenobarbital | 4 | −2 | 0 | 0 | 0 | Low | Quality points deducted for sparse data and subgroup analysis |
5 (395) | Seizure frequency | Phenytoin v sodium valproate | 4 | −1 | 0 | 0 | 0 | Moderate | Quality point deducted for subgroup analysis |
2 (147) | Seizure frequency | Phenytoin v oxcarbazepine | 4 | −2 | 0 | 0 | 0 | Low | Quality points deducted for sparse data and subgroup analysis |
1 (186) | Seizure frequency | Lamotrigine v carbamazepine | 4 | −1 | 0 | −2 | 0 | Very low | Quality point deducted for sparse data. Directness points deducted for uncertainty about epilepsy type and population restricted to older people |
What are the effects of additional treatments in people with drug-resistant generalised epilepsy? | |||||||||
3 (296) | Seizure frequency | Adding lamotrigine v adding placebo | 4 | −1 | 0 | 0 | 0 | Moderate | Quality point deducted for incomplete reporting of results |
2 (286) | Seizure frequency | Adding levetiracetam v adding placebo | 4 | −1 | 0 | 0 | 0 | Moderate | Quality point deducted for incomplete reporting in 1 RCT |
Type of evidence: 4 = RCT; 2 = Observational.Consistency: similarity of results across studies.Directness: generalisability of population or outcomes. Effect size: based on relative risk or odds ratio.