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        <datestamp>2026-09-21T06:05:19Z</datestamp>
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          <dc:title>Table 2_Efficacy, treatment retention, and tolerability of newer- versus older-generation antiseizure medications in older adults with epilepsy: a systematic review and meta-analysis.xlsx</dc:title>
          <dc:creator>Changyan Fan (25080784)</dc:creator>
          <dc:creator>Chaosheng Li (3180048)</dc:creator>
          <dc:creator>Chenyan Sui (25080787)</dc:creator>
          <dc:creator>Likun Han (14000205)</dc:creator>
          <dc:creator>Xin Gu (244758)</dc:creator>
          <dc:creator>Yong Liu (6908)</dc:creator>
          <dc:subject>Neurology and Neuromuscular Diseases</dc:subject>
          <dc:subject>antiseizure medications</dc:subject>
          <dc:subject>epilepsy</dc:subject>
          <dc:subject>meta-analysis</dc:subject>
          <dc:subject>older adults</dc:subject>
          <dc:subject>seizure freedom</dc:subject>
          <dc:subject>treatment retention</dc:subject>
          <dc:description>Objective&lt;p&gt;Older adults with epilepsy frequently have multiple comorbidities, polypharmacy, and reduced medication tolerance; therefore, ASM selection must consider seizure control, treatment persistence, and tolerability. This study compared the efficacy and safety outcomes of newer-generation and older-generation ASMs in older adults with epilepsy.&lt;/p&gt;Methods&lt;p&gt;PubMed, Embase, Web of Science Core Collection, and the Cochrane Library were searched from inception to April 30, 2026. Comparative clinical studies evaluating newer-generation versus older-generation ASMs in populations defined as older adults by the original studies were eligible. The primary outcome was seizure freedom; secondary outcomes included seizure-free retention, treatment retention, withdrawal for any reason, discontinuation due to adverse events, and adverse reactions. Risk ratios (RRs) with 95% confidence intervals (CIs) were pooled using fixed- or random-effects models according to statistical and clinical heterogeneity.&lt;/p&gt;Results&lt;p&gt;Nine studies involving 2,507 participants were included, comprising randomized, open-label, post-hoc subgroup, and retrospective evidence. Overall seizure freedom did not differ significantly between the two medication categories (RR = 1.18, 95% CI 0.80–1.76; I&lt;sup&gt;2&lt;/sup&gt; = 93%), and the restricted sensitivity analysis remained non-significant (RR = 1.11, 95% CI 0.94–1.30). No significant difference was observed in seizure-free retention. Newer-generation ASMs were associated with higher treatment retention (RR = 1.34, 95% CI 1.22–1.47), with the inverse outcome of withdrawal for any reason correspondingly lower (RR = 0.71, 95% CI 0.64–0.80); adverse-event-related discontinuation was also lower (RR = 0.54, 95% CI 0.45–0.64). In the exploratory post-stroke analysis based on two randomized studies, the random-effects estimate did not show a significant difference in seizure freedom (RR = 1.30, 95% CI 0.81–2.08; I&lt;sup&gt;2&lt;/sup&gt; = 77%).&lt;/p&gt;Conclusion&lt;p&gt;Across a small and clinically heterogeneous evidence base, seizure freedom did not clearly differ between newer- and older-generation ASMs, whereas treatment retention and adverse-event-related discontinuation favored newer-generation agents; however, the certainty of evidence was low or very low. These class-level findings should be interpreted cautiously because the medication categories were pharmacologically heterogeneous and the evidence included mixed study designs, variable age definitions, and inconsistent outcome windows.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-21T06:05:19Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fneur.2026.1902489.s002</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Table_2_Efficacy_treatment_retention_and_tolerability_of_newer-_versus_older-generation_antiseizure_medications_in_older_adults_with_epilepsy_a_systematic_review_and_meta-analysis_xlsx/33950437</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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