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Dodatno liječenje parcijalne epilepsije losigamonom

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Abstract

Background

Epilepsy is a common neurologic disorder, affecting approximately 50 million people worldwide; nearly a third of these people are not well controlled by a single antiepileptic drug (AED) and usually require treatment with a combination of two or more AEDs. In recent years, many newer AEDs have been investigated as add‐on therapy for partial epilepsy; losigamone is one of these drugs and is the focus of this systematic review. This is an update of a Cochrane review first published in 2012 (Cochrane Database of Systematic Reviews 2012, Issue 6).

Objectives

To investigate the efficacy and safety of losigamone when used as an add‐on therapy for partial epilepsy.

Search methods

We searched the Cochrane Epilepsy Group Specialized Register (16 February 2015), the Cochrane Central Register of Controlled Trials (CENTRAL, The Cochrane Library 16 February 2015) and MEDLINE (Ovid, 1946 to 16 February 2015). We searched trials registers and contacted the manufacturer of losigamone and authors of included studies for additional information. We did not impose any language restrictions.

Selection criteria

Randomized controlled, add‐on trials comparing losigamone with placebo for partial epilepsy.

Data collection and analysis

Two review authors independently assessed trial quality and extracted data. The primary outcomes were 50% or greater reduction in seizure frequency and seizure freedom; the secondary outcomes were treatment withdrawal and adverse events. Results are presented as risk ratios (RRs) with 95% confidence intervals (CIs) or 99% CIs (for the individual listed adverse events to make an allowance for multiple testing).

Main results

Two trials involving a total of 467 patients, aged over 18 years, were eligible for inclusion. Both trials assessed losigamone 1200 mg/day or 1500 mg/day as an add‐on therapy for partial epilepsy. One trial was assessed as being of good methodological quality while the other was of uncertain quality. For the efficacy outcomes, results did show patients taking losigamone were significantly more likely to achieve a 50% or greater reduction in seizure frequency (RR 1.76; 95% CI 1.14 to 2.72), but associated with a significant increase of treatment withdrawal when compared with those taking placebo (RR 2.16; 95% CI 1.28 to 3.67). For the safety outcomes, results indicated the proportion of patients who experienced adverse events in the losigamone group was higher than the placebo group (RR 1.34; 95% CI 1.00 to 1.80), dizziness was the only adverse event significantly reported in relation to losigamone (RR 3.82; 99% CI 1.69 to 8.64). The proportion of patients achieving seizure freedom was not reported in either trial report. A subgroup analysis according to different doses of losigamone showed that a higher dose of losigamone (1500 mg/day) was associated with a greater reduction in seizure frequency than lower doses, but was also associated with more dropouts due to adverse events.

Authors' conclusions

The results of this review showed losigamone did reduce seizure frequency but was associated with more treatment withdrawals when used as an add‐on therapy for people with partial epilepsy. However, trials included were of short‐term duration and uncertain quality. Future well‐designed randomized, double‐blind, placebo‐controlled trials with a longer‐term duration are needed. No new studies have been found since the last version of this review.

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.

Laički sažetak

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Losigamon kao dodatna terapija za liječenje parcijalne epilepsije

Istraživačko pitanje

Ovaj Cochrane sustavni pregled je obnovljena verzija ranije objavljenog sustavnog pregleda pod nazivom "Losigamon kao dodatna terapija za liječenje parcijalne epilepsije" koji je prethodno objavljen u Cochrane bazi sustavnih pregleda (2012, broj 6). Autori su pregledali dokaze o učinkovitosti i sigurnosti losigamona kada se rabi kao dodatni lijek za parcijalnu epilepsiju. Pronađene su dvije studije.

Dosadašnje spoznaje

Epilepsija je čest neurološki poremećaj koji pogađa približno 50 milijuna ljudi u svijetu. U gotovo trećine tih ljudi bolest se ne kontrolira dobro jednim antiepileptikom (AED, eng. antiepileptic drug) i često je potrebno liječenje s dva ili više AED (dodatna terapija). U novije vrijeme istraživani su brojni noviji AED kao dodatna terapija za parcijalnu epilepsiju. Losigamon je među tim lijekovima. Autori ovog Cochrane sustavnog pregleda su željeli ispitati učinkovitost i sigurnost losigamona kao dodatnoga lijeka za parcijalnu epilepsiju.

Obilježja studija

Dokazi se odnose na literaturu dostupnu do veljače 2015. Pronađene su dvije studije koje su procjenjivale dodatnu terapiju losigamonom za parcijalnu epilepsiju, a koje su uključile ukupno 467 pacijenata starijih od 18 godina. Obje studije su procjenjivale doze losigamona od 1200 mg/dan ili 1500 mg/dan.

Ključni rezultati

Rezultati ovog Cochrane sustavnog pregleda su pokazali da se u pacijenata koji su uzimali losigamon kao dodatnu terapiju povećala vjerojatnost smanjenja učestalosti napadaja za 50% ili više u kratkom vremenskom razdoblju; međutim povezan je s češćom nuspojavom ustezanja lijeka negoli placebo. Najučestalija nuspojava uzrokovana losigamonom je bila vrtoglavica.

Kvaliteta dokaza

Jedna studija je imala dobru metodološku kvalitetu dok za drugu kvaliteta nije bila pouzdana.

Authors' conclusions

Implications for practice

The results of this review showed that losigamone reduced seizure frequency in the short‐term, but that it was associated with more treatment‐related withdrawals when compared with placebo, for people with partial epilepsy. Losigamone seemed to be safe and well tolerated; the most frequent adverse event was dizziness.

Implications for research

Future well‐designed randomized, double blinded, placebo‐controlled trials with a longer‐term duration assessing the use of losigamone as an add‐on treatment for partial epilepsy are needed. These studies should also be designed to establish a reliable dose‐response relationship.

Summary of findings

Open in table viewer
Summary of findings for the main comparison. Losigamone compared to placebo for partial epilepsy

Losigamone compared to placebo for partial epilepsy

Patient or population: partial epilepsy
Settings: multicenter
Intervention: losigamone
Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of Participants
(studies)

Quality of the evidence
(GRADE)

Assumed risk

Corresponding risk

Placebo

Losigamone

50% or greater reduction in seizure frequency
Follow‐up: mean 8 to 12 weeks

Study population

RR 1.76
(1.14 to 2.72)

467
(2 studies)

⊕⊕⊕⊝
moderate1

132 per 1000

233 per 1000
(151 to 360)

Moderate

131 per 1000

231 per 1000
(149 to 356)

Treatment withdrawal
Follow‐up: mean 8 to 12 weeks

Study population

RR 2.16
(1.28 to 3.67)

467
(2 studies)

⊕⊕⊕⊝
moderate1

90 per 1000

194 per 1000
(115 to 330)

Moderate

88 per 1000

190 per 1000
(113 to 323)

The proportion of participants experiencing any adverse events
Follow‐up: mean 8 to 12 weeks

Study population

RR 1.34
(1.00 to 1.80)

467
(2 studies)

⊕⊕⊕⊝
moderate1

471 per 1000

631 per 1000
(471 to 848)

Moderate

482 per 1000

646 per 1000
(482 to 868)

Adverse event (dizziness)
Follow‐up: mean 8 to 12 weeks

Study population

RR 3.82
(1.69 to 8.64)

467
(2 studies)

⊕⊕⊕⊝
moderate1

63 per 1000

243 per 1000
(107 to 549)

Moderate

60 per 1000

229 per 1000
(101 to 518)

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 One of the two included trials did not describe the method used to generate the random list and did not mention allocation concealment

Background

Description of the condition

Epilepsy is a common neurological disorder, affecting approximately 50 million people worldwide (Banerjee 2009; De Boer 2008). In developing countries, the median incidence of the disease is 68.7 per 100,000 population, which is higher than that in developed countries (43.4 per 100,000 population) (Kotsopoulos 2002). It is estimated that about 30% of patients have epilepsy that is refractory to one or more agents and they are considered to be drug‐resistant. These patients often need add‐on therapy with other antiepileptic drugs (AEDs) (Schuele 2008). People with epilepsy often have psychosocial, behavioral and cognitive problems, and may place a heavy burden on society (Devinsky 1999). As reported by the World Health Organization (WHO), the overall health burden due to epilepsy accounts for 0.5% of the global burden of disease; this can be considered as more than one‐third of the diabetes burden (1.3%) (WHO 2006). In Europe, the total annual costs of epilepsy are approximately EUR 15.5 billion (Pugliatti 2007). In China, about nine million people suffer from epilepsy; the overall annual costs are approximately USD 773 per patient, which represents half the average annual income (Hong 2009).  

Description of the intervention

Losigamone is a newer AED that has been investigated as an add‐on therapy for partial seizures. When orally administered, losigamone is well absorbed through the gastrointestinal tract and reaches a peak plasma concentration within two to three hours of administration. Its plasma elimination half‐life is approximately four to seven hours (Luszczki 2009). In two double‐blind, placebo‐controlled, add‐on studies, losigamone has shown possible effects in patients with partial epilepsy (Bauer 2001; Baulac 2003). In one study, losigamone at 1200 mg/day or 1500 mg/day, in addition to three standard anticonvulsants, was tested in 264 partial epilepsy patients. A dose‐dependent reduction of seizure frequency was observed: 29.3% of patients receiving losigamone at 1500 mg/day had a 50% or greater reduction in seizure frequency, as compared to 17.2% in those receiving losigamone at 1200 mg/day and 11.8% in the placebo group (Baulac 2003). Generally, losigamone has been shown to be safe and well tolerated. The most commonly reported adverse events are dizziness, headache, somnolence, fatigue, ataxia, nausea, diplopia, abnormal vision and vertigo. No significant clinically pharmacokinetic interactions with other AEDs have been found, which allows the use of losigamone as an add‐on therapy (Bauer 2001; Baulac 2003).

How the intervention might work

The exact mechanism of action of losigamone remains unclear. Data from experimental studies have shown that losigamone stimulates the neuronal chloride channel without directly binding to γ‐aminobutyric acid (GABA), benzodiazepine or picrotoxin receptors, but it can enhance chloride influx in the absence of GABA and potentiate the effects of GABA (Dimpfel 1995; Willmore 2001). It has also been shown to reduce the frequency of spontaneous action potentials and depress repetitive firing of neurons through a decline in presynaptic activity (Draguhn 1997). Other proposed possible mechanisms by which losigamone may decrease neuronal excitability include a decrease in persistent sodium channel current and activation of potassium channel (Gebhardt 2001; Willmore 2001).

Why it is important to do this review

Randomized studies have been conducted to investigate the efficacy and safety of losigamone when used as an add‐on therapy for partial epilepsy, but they have not been systematically reviewed (Bauer 2001; Baulac 2003). This review therefore focused on the use of losigamone as an add‐on therapy for partial epilepsy, summarizing the evidence about efficacy and safety from randomized controlled trials (RCTs). This is an update of a Cochrane review first published in 2012.

Objectives

To investigate the efficacy and safety of losigamone when used as an add‐on therapy for partial epilepsy.

Methods

Criteria for considering studies for this review

Types of studies

Published or unpublished randomized controlled trials (RCTs), with no language restrictions.

Types of participants

Patients of any age with partial epilepsy (defined as simple partial, complex partial or secondary generalized tonic‐clonic seizures) that has failed to respond to one or more antiepileptic drug(s) (AEDs), or refractory partial epilepsy (defined as focal seizures) according to the definition by the International League Against Epilepsy (ILAE) (Berg 2010; Kwan 2010) are eligible.

Types of interventions

  1. The intervention (treatment) group used losigamone in addition to one or more other AEDs.

  2. The control group used placebo in addition to the same cointervention as the treatment group.

Types of outcome measures

Primary outcomes
1. Fifty per cent or greater reduction in seizure frequency

The proportion of participants with a 50% or greater reduction in seizure frequency from pre‐randomization baseline to treatment period. We chose this outcome because it is often reported in this type of study and can be calculated for studies that did not report it, provided that baseline seizure data were recorded.

2. Seizure freedom

The proportion of participants with seizure freedom during the whole treatment period.

Secondary outcomes
1. Treatment withdrawal

The proportion of participants who withdrew during the course of the treatment period for any reason was used as a measure of global effectiveness. Adverse events were usually the main reason for treatment withdrawal.

2. Adverse events

  1. The proportion of participants experiencing any adverse events.

  2. The proportion of participants experiencing any of the following individual adverse events associated with AEDs, or clinically important adverse events reported in the original articles:

    1. dizziness

    2. headache

    3. somnolence

    4. fatigue

    5. ataxia

    6. nausea

    7. diplopia

    8. abnormal vision

    9. vertigo

    10. depression.

Search methods for identification of studies

We conducted a systematic search without language restrictions to identify all relevant published and unpublished RCTs.

Electronic searches

This search was run for the original review on 1 May 2012. Subsequent searches were run on 30 January 2014 and 16 February 2015. For the latest update we searched the following databases.

  1. The Cochrane Epilepsy Group Specialized Register (16 February 2015) using the strategy outlined in Appendix 1.

  2. The Cochrane Central Register of Controlled Trials (CENTRAL, The Cochrane Library 16 February 2015) using the strategy outlined in Appendix 2.

  3. MEDLINE (Ovid, 1946 to 16 February 2015) using the strategy outlined in Appendix 3.

  4. ClinicalTrials.gov (16 February 2015) using the search terms 'losigamone AND epilepsy'.

  5. WHO International Clinical Trials Registry Platform (ICTRP) (16 February 2015) using the search terms 'losigamone AND epilepsy'.

Searching other resources

We also searched Chinese Clinical Trial Register, reference lists of included studies and review articles, and relevant journals from recent years. We contacted the pharmaceutical company that produced losigamone (Dr. Willmar Schwabe GmbH & Co.) to obtain relevant data.

Data collection and analysis

Selection of studies

Two review authors (Xiao Y, Luo M) independently read the titles and abstracts of all studies identified by the search strategy. When we had retrieved all potentially relevant papers, each review author independently evaluated the full text of each paper for inclusion. We recorded the excluded studies and the reasons for exclusion. There was no disagreement between review authors about the selection of studies for inclusion.

Data extraction and management

Two review authors (Xiao Y, Luo M) independently extracted the following information, using a data extraction form.

  • Participants: seizure types, total and number in each group, age, gender, and seizure frequency at the time of randomization.

  • Methods: study design, study duration, randomization method, allocation concealment method, and blinding methods.

  • Interventions: details of losigamone treatment, such as administration method, dosage and duration, and number of background drugs.

  • Outcomes: the proportion of participants with a 50% or greater reduction in seizure frequency, the proportion of participants with seizure freedom during the whole treatment period, the proportion of participants who withdrew during the course of the treatment period for any reason, the proportion of participants experiencing any adverse events, and individual listed adverse events.

  • Other: country and setting, publication year, sources of funding, intention‐to‐treat (ITT) analysis, and factors for heterogeneity.

There were some minor disagreements about the data extraction, however, any disagreements were resolved after discussion between review authors.

Assessment of risk of bias in included studies

Two review authors (Xiao Y, Luo M) independently assessed the risk of bias of the included studies using the 'Risk of bias' tool recommended by the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011). The 'Risk of bias' tool consists of six specific parameters: (1) sequence generation, (2) allocation concealment, (3) blinding, (4) incomplete outcome data, (5) selective outcome reporting and (6) other bias. For each entry, the judgment ('low risk' of bias, 'high risk' of bias, or 'unclear risk' of bias) was followed by a description of the design, and conduct or observations that explained the judgment (Higgins 2011). There was no disagreement in assessing the risk of bias between the review authors.

Measures of treatment effect

We managed data according to the ITT principle. For dichotomous outcomes (50% or greater reduction in seizure frequency, seizure freedom, treatment withdrawal, and adverse events), we used risk ratios (RRs) with 95% confidence intervals (CIs) to analyze the outcomes. For individual listed adverse effects, we used RR with 99% CIs to express the results to make allowance for multiple testing.

Unit of analysis issues

We did not identify any unit of analysis issues.

Dealing with missing data

We contacted study authors to obtain additional information that was not reported in the articles; unfortunately, we have not yet received a response from the authors. We could, therefore, analyze only the data that was available in the published reports.

Assessment of heterogeneity

We evaluated clinical and methodological heterogeneity of included trials by comparing the characteristics of participants (age, gender, seizure types, seizure frequency, epilepsy duration), interventions (administration method, dosage and duration, co‐interventions) and study designs (randomization, allocation concealment and blinding methods) between studies.

We evaluated statistical heterogeneity among the included studies using a Chi2 test with significance set at 0.1 and the I2 statistic. For the Chi2 test a P value of more than 0.1 was considered indicative of no significant statistical heterogeneity. If a P value was less than 0.1, we interpreted heterogeneity according to the percentage ranges of the I2 statistic as follows (Higgins 2011).

  1. 0% to 40%: might not be important;

  2. 30% to 60%: may represent moderate heterogeneity*;

  3. 50% to 90%: may represent substantial heterogeneity*;

  4. 75% to 100%: considerable heterogeneity*.

*The importance of the observed value of the I2 statistic depends on (i) the magnitude and direction of effects and (ii) the strength of evidence for heterogeneity (e.g. P value from the Chi2 test or a CI for the I2 statistic).

Assessment of reporting biases

We could not investigate potential biases of publication using funnel plots and visual inspection for asymmetry to assess reporting bias according to the approach outlined in the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011) as we identified only two studies.

Data synthesis

We used Review Manager 5.2 (RevMan 2012) to synthesize the available data. Whether we applied a fixed‐effect or a random‐effects model mainly depended on the results of the Chi2 test and the I2 statistic for heterogeneity (Higgins 2011). If a P value was more than 0.1, indicating no significant statistical heterogeneity, we used a fixed‐effect model. If a P value was less than 0.1 and the I2 statistic indicated no important or moderate heterogeneity, we used a fixed‐effect model. If a P value was less than 0.1 and the I2 statistic indicated substantial heterogeneity, we explored the factors contributing to heterogeneity first, to determine whether a subgroup analysis was needed. If the substantial heterogeneity could not be explained, we employed a random‐effects model.

Subgroup analysis and investigation of heterogeneity

We planned to perform the following subgroup analyses.

  • Different age groups (e.g. children and adolescents (less than 17 years) and adults).

  • Different doses of losigamone.

However, because of the limited data from the included studies, we could only perform the subgroup analysis according to different doses of losigamone.

Sensitivity analysis

We planned to perform the following sensitivity analysis.

  • Re‐analysis excluding studies without adequate allocation concealment or blinding.

However, because we only identified two trials, we did not perform a sensitivity analysis.

Results

Description of studies

See: Characteristics of included studies; Characteristics of excluded studies.

Results of the search

The original search on 1st May 2012 yielded a total of 29 potentially relevant articles (Cochrane Epilepsy Group Specialized Register: 5, CENTRAL: 8, MEDLINE: 16); we identified a further two relevant articles from reference lists of included studies. After reviewing the titles and abstracts we excluded 26 articles as they were not relevant or were obvious duplicate publications. Of the remaining five articles, we excluded three articles (Morris 1997; Runge 1993; Stefan 2001). Finally, two studies (Bauer 2001; Baulac 2003) were eligible to be included in the review (see Figure 1). We did not identify any ongoing trials or unpublished data. We did an updated search on 30 January 2014 and 16 February 2015 and did not identify any new studies.


Study flow diagram.

Study flow diagram.

Included studies

We included two studies that investigated the efficacy and safety of losigamone as an add‐on therapy for partial epilepsy (see Characteristics of included studies).

The first study conducted in Germany by Bauer et al (Bauer 2001) was a randomized, double‐blind, placebo‐controlled, add‐on study. The study lasted for 16 weeks and consisted of an eight‐week baseline phase and an eight‐week double‐blind treatment phase. A total of 203 patients with partial epilepsy taking no more than three AEDs prior to the study were randomized to treatment with either losigamone or placebo: 99 assigned to losigamone group and 104 to placebo; the mean age of patients in the losigamone group was 36.1 years (range 18 to 63 years) and 35.2 years (range 19 to 74 years) in the placebo group; the mean duration of epilepsy was 23.5 years in the losigamone group and 22.0 years in the placebo group; the mean frequency of partial seizures per 28 days in the losigamone group was 8.77 seizures while in the placebo group was 9.33 seizures. The dosage of losigamone administered was 750 mg/day in the first 2 days after randomization and then maintained at 1500 mg/day from the third day. The authors reported change in seizure frequency and responder rate as primary outcome measures. At the end of the eight‐week follow‐up, 171 patients finished the study; 21 patients dropped out in the losigamone treated group, and 11 patients dropped out in the placebo group. 

The second study conducted by Baulac et al (Baulac 2003) was a multicenter, randomized, double‐blind, placebo‐controlled, add‐on study. The study lasted for 28 weeks and consisted of a 12‐week baseline period, a 12‐week double‐blind treatment phase and a four‐week post‐treatment period for safety observations. A total of 264 patients with partial epilepsy, who had also had one to three AEDs prior to the study, were randomly assigned to the losigamone or placebo group: 87 patients were randomized to losigamone 1200 mg/day, 92 to losigamone 1500 mg/day and 85 to placebo. The mean age of the study population was 35.7 years, the mean duration of the disease was 21 years, and the mean seizure frequency per month before randomization was 9.2 seizures. The percentage reduction in seizure frequency and 50% or greater reduction in seizures were used as primary outcome measures. During the 12‐week double‐blind treatment period, 228 patients completed the study; 11 were withdrawn in the losigamone 1200 mg/day group, 19 in the losigamone 1500 mg/day group and six in the placebo group; 28 (77.8%) of the withdrawals were due to adverse events.

Excluded studies

We excluded both Morris 1997 and Runge 1993 because they had no control group; Stefan 2001 assessed losigamone monotherapy in patients with pharmacoresistant partial seizures undergoing presurgical evaluation (see Characteristics of excluded studies).

Risk of bias in included studies

One trial was assessed as being of good methodological quality (Baulac 2003) while the other was of uncertain quality (Bauer 2001). Overall results of all the risk of bias assessments are summarized in Figure 2 and Figure 3.


Risk of bias graph: review authors' judgments about each risk of bias item presented as percentages across all included studies.

Risk of bias graph: review authors' judgments about each risk of bias item presented as percentages across all included studies.


Risk of bias summary: review authors' judgments about each risk of bias item for each included study.

Risk of bias summary: review authors' judgments about each risk of bias item for each included study.

Allocation

Both included studies were reported as randomized. However, only Baulac 2003 mentioned the method of generation of the random list describing the use of a random number generator and the use of permuted blocks. A third party was responsible for storing the allocation sequence who was not involved in the assignment to ensure adequate allocation concealment. The other study (Bauer 2001) did not describe the method used to generate the random list and did not mention allocation concealment. We contacted the study author asking for clarification of methods used, but so far we have not had a response. Accordingly, whether the randomization and allocation concealment was adequate is unclear.

Blinding

Although both included studies (Bauer 2001; Baulac 2003) were reported as double‐blind, no additional information has been provided regarding the details of blinding, especially whether outcome assessors were blinded or not. Despite the minor flaw, we would like to judge both studies at low risk of bias in this field at present.

Incomplete outcome data

Both Bauer 2001 and Baulac 2003 provided enough information about the number of, and the reasons for dropouts, but neither of them seems balanced across groups. In Bauer 2001, the percentage dropout in the losigamone group was 21.2% (21/99) and 10.6% (11/104) in the placebo group; in Baulac 2003, the percentage of dropout in losigamone 1200 mg/day was 12.6% (11/87), losigamone 1500 mg/day was 20.7% (19/92), and placebo was 7.1% (6/85). We judged both of the studies at high risk of attrition bias.

Selective reporting

Table 1 shows the outcome reporting matrix for the review's primary and secondary outcomes. It was difficult to confirm whether all prespecified outcomes were reported as we could not obtain protocols from both included studies. Given that favorable and unfavorable results were reported in Bauer 2001 and Baulac 2003, we judged both of them to have a low risk of selective reporting bias.

Open in table viewer
Table 1. Outcome reporting matrix

Study ID
(author, date of publication)

Review's primary outcomes

Review's secondary outcomes

Other study outcomes

50% or greater reduction in seizure frequency

Seizure freedom

Treatment withdrawal

Adverse events

Change in seizure frequency

The percentage reduction in seizure frequency

Bauer 2001

×

×

Baulac 2003

×

×

√Full reporting of outcomes for treatment comparison

× No reporting of outcomes for treatment comparison

Other potential sources of bias

We did not identify other potential sources of bias for either included studies.

Effects of interventions

See: Summary of findings for the main comparison Losigamone compared to placebo for partial epilepsy

See: summary of findings Table for the main comparison

Primary outcomes

Fifty per cent or greater reduction in seizure frequency

Both trials (Bauer 2001; Baulac 2003) involving a total of 467 patients contributed to this outcome analysis; Bauer 2001 randomly allocated patients to losigamone 1500 mg/day or placebo, while Baulac 2003 allocated patients to losigamone 1200 mg/day, 1500 mg/day or placebo. When pooling these results, regardless of doses and follow‐up period, patients taking losigamone were significantly more likely to achieve a 50% or greater reduction in seizure frequency than those taking placebo (RR 1.76; 95% CI 1.14 to 2.72) (see Analysis 1.1), the test for heterogeneity indicated no significant heterogeneity (P = 0.56, I2 = 0%), so the fixed‐effect model was applied. When analyzing the results according to different doses, results did show a 50% or greater reduction in seizure frequency favored losigamone administered at 1500 mg/day compared to placebo (RR 1.94; 95% CI 1.25 to 3.01) (see Analysis 1.2), but no significant difference was detected between losigamone 1200 mg/day and placebo (RR 1.47; 95% CI 0.70 to 3.08) (see Analysis 1.3). It was not possible to do the adolescents/adults subgroup analyses because both trials only recruited patients aged over 18 years.

Seizure freedom

The proportion of participants with seizure freedom during the whole treatment period was not reported in either study.

Secondary outcomes

Treatment withdrawal

The number of treatment withdrawals and their reasons were carefully reported in both included trials (Bauer 2001; Baulac 2003). Adverse events were the main reason for treatment withdrawal; other reasons included lack of efficacy, increase of seizure frequency, status epilepticus and poor compliance. A pooled analysis of both studies, regardless of doses and follow‐up period, indicated that patients receiving losigamone experienced a significant increase in treatment withdrawal for any reason, compared to those receiving placebo (RR 2.16; 95% CI 1.28 to 3.67) (see Analysis 2.1), the test for heterogeneity indicated no significant heterogeneity (P = 0.76, I2 = 0%), so the fixed‐effect model was applied. When analyzing the results according to different doses, the dose of losigamone 1500 mg/day resulted in an increased risk of treatment withdrawal compared with placebo (RR 2.34; 95% CI 1.38 to 3.99) (see Analysis 2.2), while the dose of losigamone 1200 mg/day was not likely to lead to significant difference between both groups (RR 1.79; 95% CI 0.69 to 4.63) (see Analysis 2.3).

Adverse events

Both trials reported adverse events according to the WHO Adverse Reaction Terminology (WHO‐ART). In Bauer 2001, the adverse events analysis was performed according to the categorization of treatment‐emergent signs and symptoms (e.g. central and peripheral nervous system disorders, body as a whole ‐ general considerations, vision disorders, psychiatric disorders, gastrointestinal system disorders), only the most frequent adverse events were listed as individual symptoms; overall, they found no significant difference between treatment groups with regard to these adverse events during short‐term follow‐up period. In contrast, in Baulac 2003, all listed adverse events were individual symptoms.

Therefore, individual listed adverse event analysis was mainly based on the later study due to the method of reporting results. The proportion of patients receiving losigamone was higher than those receiving placebo in the occurrence of any adverse events during short‐term follow‐up period, however, the difference was not significant (RR 1.34; 95% CI 1.00 to 1.80) (see Analysis 3.1). A random‐effects model was applied because of the possible substantial heterogeneity (P = 0.10, I2 = 64%), but when re‐analyzing it under a fixed‐effect model, a significant difference was detected (RR 1.33; 95% CI 1.12 to 1.57) (see Analysis 3.2). When analyzing the results according to different doses, the proportion of patients receiving a dose of losigamone 1500 mg/day was more likely to have an adverse event than those taking placebo (RR 1.40; 95% CI 1.14 to 1.71) (see Analysis 3.1), while no significant difference was detected between the dose of losigamone 1200 mg/day and placebo (RR 1.06; 95% CI 0.83 to 1.34) (see Analysis 3.1).

A pooling analysis of the individual listed adverse events indicated that dizziness was the only adverse event that was significantly more likely to occur in the losigamone group than in the placebo group (RR 3.82; 99% CI 1.69 to 8.64) (see Analysis 3.3), there was no significant heterogeneity (P = 0.21, I2 = 37%), so the fixed‐effect model was applied. The incidence of other adverse events was not significantly difference between treatment groups: headache (RR 1.19; 99% CI 0.43 to 3.30) (see Analysis 3.4); somnolence (RR 2.26; 99% CI 0.57 to 8.93) (see Analysis 3.5); fatigue (RR 2.26; 99% CI 0.57 to 8.93) (see Analysis 3.6); ataxia (RR 10.03; 99% CI 0.24 to 411.20) (see Analysis 3.7); nausea (RR 0.85; 99% CI 0.21 to 3.45) (see Analysis 3.8); diplopia (RR 2.85; 99% CI 0.59 to 13.70) (see Analysis 3.9); abnormal vision (RR 2.37; 99% CI 0.48 to 11.68) (see Analysis 3.10); vertigo (RR 6.17; 99% CI 0.44 to 87.50) (see Analysis 3.11); depression (RR 0.63; 99% CI 0.09 to 4.40) (see Analysis 3.12). When analyzing the results according to different doses, patients receiving losigamone 1500 mg/day were associated with significantly increased rates of dizziness than placebo (RR 3.96; 99% CI 1.79 to 8.76) (see Analysis 3.3) but there was no significant difference in other adverse events between both treatment groups: headache (RR 1.50; 99% CI 0.50 to 4.47); somnolence (RR 2.77; 99% CI 0.66 to 11.65); fatigue (RR 2.77; 99% CI 0.66 to 11.65); ataxia (RR 10.17; 99% CI 0.23 to 448.02); nausea (RR 1.29; 99% CI 0.30 to 5.56); diplopia (RR 3.39; 99% CI 0.66 to 17.33); abnormal vision (RR 3.08; 99% CI 0.59 to 16.05); vertigo (RR 6.47; 99% CI 0.42 to 98.79) and depression (RR 0.92; 99% CI 0.12 to 7.30). However, losigamone 1200 mg/day did not show any significant difference from placebo on all listed adverse events: dizziness (RR 5.37; 99% CI 0.77 to 37.42); headache (RR 0.85; 99% CI 0.24 to 3.06); somnolence (RR 1.71; 99% CI 0.36 to 8.19); fatigue (RR 1.71; 99% CI 0.36 to 8.19); ataxia (RR 10.75; 99% CI 0.24 to 473.22); nausea (RR 0.39; 99% CI 0.05 to 3.25); diplopia (RR 2.28; 99% CI 0.40 to 12.90); abnormal vision (RR 1.63; 99% CI 0.26 to 10.25); vertigo (RR 5.86; 99% CI 0.37 to 92.10) and depression (RR 0.98; 99% CI 0.12 to 7.71).

Discussion

Summary of main results

This systematic review assessed the short‐term efficacy and safety of losigamone administered as an add‐on therapy for partial epilepsy. Two RCTs involving a total of 467 patients contributed to the analysis; both trials reported a dose of losigamone 1200 mg/day or 1500 mg/day in addition to one to three AEDs for epilepsy patients older than 18 years. We assessed one trial (Baulac 2003) as good quality, and the other one (Bauer 2001) of uncertain quality (see: Risk of bias in included studies). For the efficacy outcomes, results did show patients taking losigamone were significantly more likely to achieve a 50% or greater reduction in seizure frequency, but this was associated with a significant increase in treatment withdrawal when compared with those taking placebo. For the safety outcomes, results have indicated the proportion of patients who experienced adverse events in the losigamone group was higher than the placebo group. Dizziness was the only adverse event significantly related to losigamone; other adverse events (headache, somnolence, fatigue, ataxia, nausea, diplopia, abnormal vision, vertigo, depression) did not differ significantly between both groups.

A subgroup analysis according to different doses of losigamone has indicated that taking a higher dose of 1500 mg/day could increase the proportion of patients who achieved a 50% or greater reduction in seizure frequency, but it would also lead to an elevated risk of treatment withdrawal and adverse events (particularly dizziness). Taking a relatively low dose of losigamone 1200 mg/day did not show any significant difference in terms of all outcomes analysis.

Overall completeness and applicability of evidence

As a result of the insufficient number of included trials with placebo‐controlled design, short‐term duration and uncertain quality in this review, it is difficult to give any recommendations for current clinical practice of losigamone as an add‐on therapy for partial epilepsy. In this review, results suggest that the higher dose of losigamone 1500 mg/day seems a better starting dose according to its efficacy in reducing seizure frequency, but it is associated with more dropouts due to adverse events. Furthermore, because both of the included trials were focused on the adjunctive therapy of losigamone in partial epilepsy during a short‐term follow‐up (8 to 12 weeks), and recruited patients were only aged over 18 years, there is still no evidence about the efficacy and safety of losigamone in children and adolescents, and no conclusion can be drawn about the long‐term efficacy of losigamone.

Quality of the evidence

We only assessed one trial (Baulac 2003) as being of good quality; it used a double‐blind design, and had an adequate method of randomization and allocation concealment. We assessed the other trial (Bauer 2001) as being of uncertain quality; it did not describe the method used to generate the random list and did not mention allocation concealment, although a double‐blind design was used. Unclear methods of randomization and allocation concealment contribute to high‐risk performance and detection bias and may therefore lead to an overestimation of intervention effects (Schulz 1995).

It is noteworthy that both included trials reported a sample size calculation and performed an ITT analysis to provide adequate statistical power and an unbiased comparison among the treatment groups. In addition, no significant clinical heterogeneity was detected except for the different doses of losigamone used.

Potential biases in the review process

Potential biases from the trials

Although we undertook an extensive and comprehensive search to minimize bias in the review process, we could not confirm whether other studies with negative findings exist, because trials with negative findings are not published as often as trials with positive findings (Hopewell 2009). In addition, we did not receive further unreported data from correspondence with the study authors.

Potential biases from the review authors

There were no potential biases from the review authors in the review process. In the preparation of this review, two review authors independently read and screened trials retrieved for inclusion, independently completed data extraction and assessed the quality of included trials to minimize potential biases. No conflict of interests were found in relation to the review authors of this review.

Agreements and disagreements with other studies or reviews

The efficacy and safety of losigamone when used as an add‐on therapy for partial epilepsy has not been systematically reviewed previously.

Study flow diagram.
Figures and Tables -
Figure 1

Study flow diagram.

Risk of bias graph: review authors' judgments about each risk of bias item presented as percentages across all included studies.
Figures and Tables -
Figure 2

Risk of bias graph: review authors' judgments about each risk of bias item presented as percentages across all included studies.

Risk of bias summary: review authors' judgments about each risk of bias item for each included study.
Figures and Tables -
Figure 3

Risk of bias summary: review authors' judgments about each risk of bias item for each included study.

Comparison 1 Losigamone versus placebo: 50% or greater reduction in seizure frequency, Outcome 1 All doses.
Figures and Tables -
Analysis 1.1

Comparison 1 Losigamone versus placebo: 50% or greater reduction in seizure frequency, Outcome 1 All doses.

Comparison 1 Losigamone versus placebo: 50% or greater reduction in seizure frequency, Outcome 2 1500 mg/day.
Figures and Tables -
Analysis 1.2

Comparison 1 Losigamone versus placebo: 50% or greater reduction in seizure frequency, Outcome 2 1500 mg/day.

Comparison 1 Losigamone versus placebo: 50% or greater reduction in seizure frequency, Outcome 3 1200 mg/day.
Figures and Tables -
Analysis 1.3

Comparison 1 Losigamone versus placebo: 50% or greater reduction in seizure frequency, Outcome 3 1200 mg/day.

Comparison 2 Losigamone versus placebo: treatment withdrawal, Outcome 1 All doses.
Figures and Tables -
Analysis 2.1

Comparison 2 Losigamone versus placebo: treatment withdrawal, Outcome 1 All doses.

Comparison 2 Losigamone versus placebo: treatment withdrawal, Outcome 2 1500 mg/day.
Figures and Tables -
Analysis 2.2

Comparison 2 Losigamone versus placebo: treatment withdrawal, Outcome 2 1500 mg/day.

Comparison 2 Losigamone versus placebo: treatment withdrawal, Outcome 3 1200 mg/day.
Figures and Tables -
Analysis 2.3

Comparison 2 Losigamone versus placebo: treatment withdrawal, Outcome 3 1200 mg/day.

Comparison 3 Losigamone versus placebo: adverse events, Outcome 1 The proportion of participants experiencing any adverse events (random model).
Figures and Tables -
Analysis 3.1

Comparison 3 Losigamone versus placebo: adverse events, Outcome 1 The proportion of participants experiencing any adverse events (random model).

Comparison 3 Losigamone versus placebo: adverse events, Outcome 2 The proportion of participants experiencing any adverse events (fixed model).
Figures and Tables -
Analysis 3.2

Comparison 3 Losigamone versus placebo: adverse events, Outcome 2 The proportion of participants experiencing any adverse events (fixed model).

Comparison 3 Losigamone versus placebo: adverse events, Outcome 3 Dizziness.
Figures and Tables -
Analysis 3.3

Comparison 3 Losigamone versus placebo: adverse events, Outcome 3 Dizziness.

Comparison 3 Losigamone versus placebo: adverse events, Outcome 4 Headache.
Figures and Tables -
Analysis 3.4

Comparison 3 Losigamone versus placebo: adverse events, Outcome 4 Headache.

Comparison 3 Losigamone versus placebo: adverse events, Outcome 5 Somnolence.
Figures and Tables -
Analysis 3.5

Comparison 3 Losigamone versus placebo: adverse events, Outcome 5 Somnolence.

Comparison 3 Losigamone versus placebo: adverse events, Outcome 6 Fatigue.
Figures and Tables -
Analysis 3.6

Comparison 3 Losigamone versus placebo: adverse events, Outcome 6 Fatigue.

Comparison 3 Losigamone versus placebo: adverse events, Outcome 7 Ataxia.
Figures and Tables -
Analysis 3.7

Comparison 3 Losigamone versus placebo: adverse events, Outcome 7 Ataxia.

Comparison 3 Losigamone versus placebo: adverse events, Outcome 8 Nausea.
Figures and Tables -
Analysis 3.8

Comparison 3 Losigamone versus placebo: adverse events, Outcome 8 Nausea.

Comparison 3 Losigamone versus placebo: adverse events, Outcome 9 Diplopia.
Figures and Tables -
Analysis 3.9

Comparison 3 Losigamone versus placebo: adverse events, Outcome 9 Diplopia.

Comparison 3 Losigamone versus placebo: adverse events, Outcome 10 Abnormal vision.
Figures and Tables -
Analysis 3.10

Comparison 3 Losigamone versus placebo: adverse events, Outcome 10 Abnormal vision.

Comparison 3 Losigamone versus placebo: adverse events, Outcome 11 Vertigo.
Figures and Tables -
Analysis 3.11

Comparison 3 Losigamone versus placebo: adverse events, Outcome 11 Vertigo.

Comparison 3 Losigamone versus placebo: adverse events, Outcome 12 Depression.
Figures and Tables -
Analysis 3.12

Comparison 3 Losigamone versus placebo: adverse events, Outcome 12 Depression.

Summary of findings for the main comparison. Losigamone compared to placebo for partial epilepsy

Losigamone compared to placebo for partial epilepsy

Patient or population: partial epilepsy
Settings: multicenter
Intervention: losigamone
Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of Participants
(studies)

Quality of the evidence
(GRADE)

Assumed risk

Corresponding risk

Placebo

Losigamone

50% or greater reduction in seizure frequency
Follow‐up: mean 8 to 12 weeks

Study population

RR 1.76
(1.14 to 2.72)

467
(2 studies)

⊕⊕⊕⊝
moderate1

132 per 1000

233 per 1000
(151 to 360)

Moderate

131 per 1000

231 per 1000
(149 to 356)

Treatment withdrawal
Follow‐up: mean 8 to 12 weeks

Study population

RR 2.16
(1.28 to 3.67)

467
(2 studies)

⊕⊕⊕⊝
moderate1

90 per 1000

194 per 1000
(115 to 330)

Moderate

88 per 1000

190 per 1000
(113 to 323)

The proportion of participants experiencing any adverse events
Follow‐up: mean 8 to 12 weeks

Study population

RR 1.34
(1.00 to 1.80)

467
(2 studies)

⊕⊕⊕⊝
moderate1

471 per 1000

631 per 1000
(471 to 848)

Moderate

482 per 1000

646 per 1000
(482 to 868)

Adverse event (dizziness)
Follow‐up: mean 8 to 12 weeks

Study population

RR 3.82
(1.69 to 8.64)

467
(2 studies)

⊕⊕⊕⊝
moderate1

63 per 1000

243 per 1000
(107 to 549)

Moderate

60 per 1000

229 per 1000
(101 to 518)

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect.
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate.

1 One of the two included trials did not describe the method used to generate the random list and did not mention allocation concealment

Figures and Tables -
Summary of findings for the main comparison. Losigamone compared to placebo for partial epilepsy
Table 1. Outcome reporting matrix

Study ID
(author, date of publication)

Review's primary outcomes

Review's secondary outcomes

Other study outcomes

50% or greater reduction in seizure frequency

Seizure freedom

Treatment withdrawal

Adverse events

Change in seizure frequency

The percentage reduction in seizure frequency

Bauer 2001

×

×

Baulac 2003

×

×

√Full reporting of outcomes for treatment comparison

× No reporting of outcomes for treatment comparison

Figures and Tables -
Table 1. Outcome reporting matrix
Comparison 1. Losigamone versus placebo: 50% or greater reduction in seizure frequency

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 All doses Show forest plot

2

467

Risk Ratio (M‐H, Fixed, 95% CI)

1.76 [1.14, 2.72]

2 1500 mg/day Show forest plot

2

380

Risk Ratio (M‐H, Fixed, 95% CI)

1.94 [1.25, 3.01]

3 1200 mg/day Show forest plot

1

172

Risk Ratio (M‐H, Fixed, 95% CI)

1.47 [0.70, 3.08]

Figures and Tables -
Comparison 1. Losigamone versus placebo: 50% or greater reduction in seizure frequency
Comparison 2. Losigamone versus placebo: treatment withdrawal

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 All doses Show forest plot

2

467

Risk Ratio (M‐H, Fixed, 95% CI)

2.16 [1.28, 3.67]

2 1500 mg/day Show forest plot

2

380

Risk Ratio (M‐H, Fixed, 95% CI)

2.34 [1.38, 3.99]

3 1200 mg/day Show forest plot

1

172

Risk Ratio (M‐H, Fixed, 95% CI)

1.79 [0.69, 4.63]

Figures and Tables -
Comparison 2. Losigamone versus placebo: treatment withdrawal
Comparison 3. Losigamone versus placebo: adverse events

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 The proportion of participants experiencing any adverse events (random model) Show forest plot

2

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

1.1 All doses

2

467

Risk Ratio (M‐H, Random, 95% CI)

1.34 [1.00, 1.80]

1.2 1200 mg/day

1

172

Risk Ratio (M‐H, Random, 95% CI)

1.06 [0.83, 1.34]

1.3 1500 mg/day

2

380

Risk Ratio (M‐H, Random, 95% CI)

1.40 [1.14, 1.71]

2 The proportion of participants experiencing any adverse events (fixed model) Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Subtotals only

2.1 All doses

2

467

Risk Ratio (M‐H, Fixed, 95% CI)

1.33 [1.12, 1.57]

3 Dizziness Show forest plot

2

Risk Ratio (M‐H, Fixed, 99% CI)

Subtotals only

3.1 All doses

2

467

Risk Ratio (M‐H, Fixed, 99% CI)

3.82 [1.69, 8.64]

3.2 1200 mg/day

1

172

Risk Ratio (M‐H, Fixed, 99% CI)

5.37 [0.77, 37.42]

3.3 1500 mg/day

2

380

Risk Ratio (M‐H, Fixed, 99% CI)

3.96 [1.79, 8.76]

4 Headache Show forest plot

1

Risk Ratio (M‐H, Fixed, 99% CI)

Subtotals only

4.1 All doses

1

264

Risk Ratio (M‐H, Fixed, 99% CI)

1.19 [0.43, 3.30]

4.2 1200 mg/day

1

172

Risk Ratio (M‐H, Fixed, 99% CI)

0.85 [0.24, 3.06]

4.3 1500 mg/day

1

177

Risk Ratio (M‐H, Fixed, 99% CI)

1.50 [0.50, 4.47]

5 Somnolence Show forest plot

1

Risk Ratio (M‐H, Fixed, 99% CI)

Subtotals only

5.1 All doses

1

264

Risk Ratio (M‐H, Fixed, 99% CI)

2.26 [0.57, 8.93]

5.2 1200 mg/day

1

172

Risk Ratio (M‐H, Fixed, 99% CI)

1.71 [0.36, 8.19]

5.3 1500 mg/day

1

177

Risk Ratio (M‐H, Fixed, 99% CI)

2.77 [0.66, 11.65]

6 Fatigue Show forest plot

1

Risk Ratio (M‐H, Fixed, 99% CI)

Subtotals only

6.1 All doses

1

264

Risk Ratio (M‐H, Fixed, 99% CI)

2.26 [0.57, 8.93]

6.2 1200 mg/day

1

172

Risk Ratio (M‐H, Fixed, 99% CI)

1.71 [0.36, 8.19]

6.3 1500 mg/day

1

177

Risk Ratio (M‐H, Fixed, 99% CI)

2.77 [0.66, 11.65]

7 Ataxia Show forest plot

1

Risk Ratio (M‐H, Fixed, 99% CI)

Subtotals only

7.1 All doses

1

264

Risk Ratio (M‐H, Fixed, 99% CI)

10.03 [0.24, 411.20]

7.2 1200 mg/day

1

172

Risk Ratio (M‐H, Fixed, 99% CI)

10.75 [0.24, 473.22]

7.3 1500 mg/day

1

177

Risk Ratio (M‐H, Fixed, 99% CI)

10.17 [0.23, 448.02]

8 Nausea Show forest plot

1

Risk Ratio (M‐H, Fixed, 99% CI)

Subtotals only

8.1 All doses

1

264

Risk Ratio (M‐H, Fixed, 99% CI)

0.85 [0.21, 3.45]

8.2 1200 mg/day

1

172

Risk Ratio (M‐H, Fixed, 99% CI)

0.39 [0.05, 3.25]

8.3 1500 mg/day

1

177

Risk Ratio (M‐H, Fixed, 99% CI)

1.29 [0.30, 5.56]

9 Diplopia Show forest plot

1

Risk Ratio (M‐H, Fixed, 99% CI)

Subtotals only

9.1 All doses

1

264

Risk Ratio (M‐H, Fixed, 99% CI)

2.85 [0.59, 13.70]

9.2 1200 mg/day

1

172

Risk Ratio (M‐H, Fixed, 99% CI)

2.28 [0.40, 12.90]

9.3 1500 mg/day

1

177

Risk Ratio (M‐H, Fixed, 99% CI)

3.39 [0.66, 17.33]

10 Abnormal vision Show forest plot

1

Risk Ratio (M‐H, Fixed, 99% CI)

Subtotals only

10.1 All doses

1

264

Risk Ratio (M‐H, Fixed, 99% CI)

2.37 [0.48, 11.68]

10.2 1200 mg/day

1

172

Risk Ratio (M‐H, Fixed, 99% CI)

1.63 [0.26, 10.25]

11 Vertigo Show forest plot

1

Risk Ratio (M‐H, Fixed, 99% CI)

Subtotals only

11.1 All doses

1

264

Risk Ratio (M‐H, Fixed, 99% CI)

6.17 [0.44, 87.50]

11.2 1200 mg/day

1

172

Risk Ratio (M‐H, Fixed, 99% CI)

5.86 [0.37, 92.10]

11.3 1500 mg/day

1

177

Risk Ratio (M‐H, Fixed, 99% CI)

6.47 [0.42, 98.79]

12 Depression Show forest plot

1

Risk Ratio (M‐H, Fixed, 99% CI)

Subtotals only

12.1 All doses

1

264

Risk Ratio (M‐H, Fixed, 99% CI)

0.63 [0.09, 4.40]

12.2 1200 mg/day

1

172

Risk Ratio (M‐H, Fixed, 99% CI)

0.98 [0.12, 7.71]

12.3 1500 mg/day

1

177

Risk Ratio (M‐H, Fixed, 99% CI)

0.92 [0.12, 7.30]

Figures and Tables -
Comparison 3. Losigamone versus placebo: adverse events