Eslicarbazepine acetate in post-stroke epilepsy: Clinical practice evidence from Euro-Esli
| Main Author: | |
|---|---|
| Publication Date: | 2020 |
| Other Authors: | , , , , |
| Format: | Article |
| Language: | eng |
| Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
| Download full: | http://hdl.handle.net/10400.16/2476 |
Summary: | Objectives: To assess the effectiveness and safety/tolerability of eslicarbazepine acetate (ESL) in patients included in the Euro-Esli study who had focal seizures associated with post-stroke epilepsy (PSE). Materials and methods: Euro-Esli was a pooled analysis of 14 European clinical practice studies. Effectiveness assessments (evaluated after 3, 6 and 12 months of ESL treatment and at final follow-up ["last visit"]) included rates of response (≥50% seizure frequency reduction), seizure freedom (no seizures since at least the prior visit) and retention. Safety/tolerability was assessed throughout ESL treatment by evaluating adverse events (AEs) and discontinuation due to AEs. A post hoc analysis was conducted of patients with PSE versus patients without PSE ("non-PSE"). Results: Of 1656 patients included in the analysis, 76 (4.6%) had PSE and 1580 (95.4%) had non-PSE. Compared with non-PSE patients, PSE patients were significantly older, had significantly shorter epilepsy duration, significantly lower total baseline seizure frequency, and were treated with significantly fewer prior and concomitant antiepileptic drugs (P < .001 for all). At the last visit, the responder rate was significantly higher in PSE versus non-PSE patients (72.9% vs 60.6%; P = .040), as was the seizure freedom rate (48.6% vs 31.7%; P = .003). After 12 months, retention was significantly higher in PSE versus non-PSE patients (87.8% vs 77.4%; P = .035). The incidence of AEs was similar for PSE versus non-PSE patients (36.0% vs 35.8%; P = .966). Conclusions: These findings suggest that ESL may be an effective and well-tolerated treatment option for patients with focal seizures due to PSE. |
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Eslicarbazepine acetate in post-stroke epilepsy: Clinical practice evidence from Euro-EsliEpilepsyeslicarbazepine acetateseizuresstrokeObjectives: To assess the effectiveness and safety/tolerability of eslicarbazepine acetate (ESL) in patients included in the Euro-Esli study who had focal seizures associated with post-stroke epilepsy (PSE). Materials and methods: Euro-Esli was a pooled analysis of 14 European clinical practice studies. Effectiveness assessments (evaluated after 3, 6 and 12 months of ESL treatment and at final follow-up ["last visit"]) included rates of response (≥50% seizure frequency reduction), seizure freedom (no seizures since at least the prior visit) and retention. Safety/tolerability was assessed throughout ESL treatment by evaluating adverse events (AEs) and discontinuation due to AEs. A post hoc analysis was conducted of patients with PSE versus patients without PSE ("non-PSE"). Results: Of 1656 patients included in the analysis, 76 (4.6%) had PSE and 1580 (95.4%) had non-PSE. Compared with non-PSE patients, PSE patients were significantly older, had significantly shorter epilepsy duration, significantly lower total baseline seizure frequency, and were treated with significantly fewer prior and concomitant antiepileptic drugs (P < .001 for all). At the last visit, the responder rate was significantly higher in PSE versus non-PSE patients (72.9% vs 60.6%; P = .040), as was the seizure freedom rate (48.6% vs 31.7%; P = .003). After 12 months, retention was significantly higher in PSE versus non-PSE patients (87.8% vs 77.4%; P = .035). The incidence of AEs was similar for PSE versus non-PSE patients (36.0% vs 35.8%; P = .966). Conclusions: These findings suggest that ESL may be an effective and well-tolerated treatment option for patients with focal seizures due to PSE.Wiley-BlackwellRepositório Científico da Unidade Local de Saúde de Santo AntónioSales, FranciscoChaves, JoãoMcMurray, RobLoureiro, RuiFernandes, HélderVillanueva, Vicente2021-06-17T14:42:21Z2020-122020-12-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.16/2476eng1600-040410.1111/ane.13323info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-26T10:09:25Zoai:repositorio.chporto.pt:10400.16/2476Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T21:20:59.171089Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
| dc.title.none.fl_str_mv |
Eslicarbazepine acetate in post-stroke epilepsy: Clinical practice evidence from Euro-Esli |
| title |
Eslicarbazepine acetate in post-stroke epilepsy: Clinical practice evidence from Euro-Esli |
| spellingShingle |
Eslicarbazepine acetate in post-stroke epilepsy: Clinical practice evidence from Euro-Esli Sales, Francisco Epilepsy eslicarbazepine acetate seizures stroke |
| title_short |
Eslicarbazepine acetate in post-stroke epilepsy: Clinical practice evidence from Euro-Esli |
| title_full |
Eslicarbazepine acetate in post-stroke epilepsy: Clinical practice evidence from Euro-Esli |
| title_fullStr |
Eslicarbazepine acetate in post-stroke epilepsy: Clinical practice evidence from Euro-Esli |
| title_full_unstemmed |
Eslicarbazepine acetate in post-stroke epilepsy: Clinical practice evidence from Euro-Esli |
| title_sort |
Eslicarbazepine acetate in post-stroke epilepsy: Clinical practice evidence from Euro-Esli |
| author |
Sales, Francisco |
| author_facet |
Sales, Francisco Chaves, João McMurray, Rob Loureiro, Rui Fernandes, Hélder Villanueva, Vicente |
| author_role |
author |
| author2 |
Chaves, João McMurray, Rob Loureiro, Rui Fernandes, Hélder Villanueva, Vicente |
| author2_role |
author author author author author |
| dc.contributor.none.fl_str_mv |
Repositório Científico da Unidade Local de Saúde de Santo António |
| dc.contributor.author.fl_str_mv |
Sales, Francisco Chaves, João McMurray, Rob Loureiro, Rui Fernandes, Hélder Villanueva, Vicente |
| dc.subject.por.fl_str_mv |
Epilepsy eslicarbazepine acetate seizures stroke |
| topic |
Epilepsy eslicarbazepine acetate seizures stroke |
| description |
Objectives: To assess the effectiveness and safety/tolerability of eslicarbazepine acetate (ESL) in patients included in the Euro-Esli study who had focal seizures associated with post-stroke epilepsy (PSE). Materials and methods: Euro-Esli was a pooled analysis of 14 European clinical practice studies. Effectiveness assessments (evaluated after 3, 6 and 12 months of ESL treatment and at final follow-up ["last visit"]) included rates of response (≥50% seizure frequency reduction), seizure freedom (no seizures since at least the prior visit) and retention. Safety/tolerability was assessed throughout ESL treatment by evaluating adverse events (AEs) and discontinuation due to AEs. A post hoc analysis was conducted of patients with PSE versus patients without PSE ("non-PSE"). Results: Of 1656 patients included in the analysis, 76 (4.6%) had PSE and 1580 (95.4%) had non-PSE. Compared with non-PSE patients, PSE patients were significantly older, had significantly shorter epilepsy duration, significantly lower total baseline seizure frequency, and were treated with significantly fewer prior and concomitant antiepileptic drugs (P < .001 for all). At the last visit, the responder rate was significantly higher in PSE versus non-PSE patients (72.9% vs 60.6%; P = .040), as was the seizure freedom rate (48.6% vs 31.7%; P = .003). After 12 months, retention was significantly higher in PSE versus non-PSE patients (87.8% vs 77.4%; P = .035). The incidence of AEs was similar for PSE versus non-PSE patients (36.0% vs 35.8%; P = .966). Conclusions: These findings suggest that ESL may be an effective and well-tolerated treatment option for patients with focal seizures due to PSE. |
| publishDate |
2020 |
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2020-12 2020-12-01T00:00:00Z 2021-06-17T14:42:21Z |
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http://hdl.handle.net/10400.16/2476 |
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eng |
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1600-0404 10.1111/ane.13323 |
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Wiley-Blackwell |
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Wiley-Blackwell |
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