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        <identifier>oai:figshare.com:article/34009860</identifier>
        <datestamp>2026-09-28T05:46:51Z</datestamp>
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          <dc:title>Data Sheet 4_Perioperative intravenous lidocaine for the prevention of chronic postsurgical pain: a systematic review and meta-analysis of randomized controlled trials.pdf</dc:title>
          <dc:creator>Wei-Jing Zhu (25119831)</dc:creator>
          <dc:creator>Ran An (456243)</dc:creator>
          <dc:creator>Qian-Yun Pang (14849779)</dc:creator>
          <dc:creator>Xiao-Long Liang (14849776)</dc:creator>
          <dc:subject>Foetal Development and Medicine</dc:subject>
          <dc:subject>chronic postsurgical pain</dc:subject>
          <dc:subject>intravenous lidocaine</dc:subject>
          <dc:subject>local anesthetic systemic toxicity</dc:subject>
          <dc:subject>meta-analysis</dc:subject>
          <dc:subject>neuropathic pain</dc:subject>
          <dc:subject>perioperative analgesia</dc:subject>
          <dc:subject>safety monitoring</dc:subject>
          <dc:subject>systematic review</dc:subject>
          <dc:description>Background&lt;p&gt;Chronic postsurgical pain (CPSP) poses a significant clinical burden, yet the efficacy of perioperative intravenous lidocaine for its prevention remains inconclusive. This meta-analysis evaluates its preventive efficacy and administration regimens.&lt;/p&gt;Methods&lt;p&gt;PubMed, EMBASE, and the Cochrane Library were searched from database inception to a prespecified cutoff of June 1, 2025; final electronic searches were run on June 8, 2025, to identify randomized controlled trials (RCTs) comparing perioperative intravenous lidocaine with placebo/standard care in adults. Primary outcomes were CPSP incidence at 3 and 6 months postoperatively.&lt;/p&gt;Results&lt;p&gt;Eighteen RCTs (1,391 patients) were included. Intravenous lidocaine significantly reduced CPSP incidence (RR = 0.67; 95% CI: 0.53 to 0.85; P = 0.001) and neuropathic pain risk (RR = 0.60; 95% CI: 0.43 to 0.85; P = 0.004) at 3 months. However, the reduction in the incidence of CPSP was not statistically significant at 6 months (RR = 0.68; 95% CI: 0.41 to 1.12; P = 0.13). Exploratory subgroup analyses of CPSP incidence at 3 months showed favorable pooled estimates in selected surgery and administration-regimen categories; however, they did not demonstrate a statistically significant difference between regimen categories. Safety assessment was limited by inconsistent adverse-event reporting and limited pharmacokinetic monitoring.&lt;/p&gt;Conclusion&lt;p&gt;Perioperative intravenous lidocaine reduces CPSP at 3 months, but evidence of an effect on CPSP incidence at 6 months remains inconclusive. Future trials should incorporate structured pharmacokinetic monitoring and exposure-response analyses and evaluate lidocaine's additive value alongside optimal regional anesthesia.&lt;/p&gt;Systematic Review Registration&lt;p&gt;PROSPERO, https://www.crd.york.ac.uk/PROSPERO/view/CRD420251063756, identifier CRD420251063756.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-28T05:46:51Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fmed.2026.1927770.s003</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Data_Sheet_4_Perioperative_intravenous_lidocaine_for_the_prevention_of_chronic_postsurgical_pain_a_systematic_review_and_meta-analysis_of_randomized_controlled_trials_pdf/34009860</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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