摘要
Acute progressive cerebral infarction (APCI) is marked by worsening symptoms and neurological decline with high mortality.This study aimed to compare the clinical efficacy of edaravone (Eda) and edaravone dexborneol (Eda.B) in APCI treatment.Clinical data from 98 APCI patients were retrospectively analysed: 48 received Eda and 50 received Eda.B intravenously for 2 weeks.Hemorheological parameters, neurological and cognitive function (NIHSS, MoCA, BI), serum inflammatory and oxidative stress markers (IL-6, IL-17, IL-1, MMP-9, MDA, SOD, GSH-Px), and cerebral perfusion (MRI-based) were evaluated.Compared to Eda, Eda.B significantly reduced blood viscosity indices and erythrocyte sedimentation rate, improved NIHSS, MoCA, and BI scores, and favourably modulated inflammatory-oxidative markers.Eda.B also enhanced cerebral blood volume and flow, while reducing mean transit time and time to peak.The clinical efficacy rate was higher in the Eda.B group (96.0% vs. 83.3%,p < 0.05), with similar adverse reaction rates (16.0% vs. 25.0%,p > 0.05).In conclusion, Eda.B showed superior effectiveness in improving neurological and cognitive function, cerebral perfusion, and reducing inflammation and oxidative stress in APCI patients. RezumatInfarctul cerebral acut progresiv (APCI) se caracterizeaz prin agravarea rapid a simptomelor i declin neurologic accentuat, fiind asociat cu o mortalitate ridicat.Acest studiu a comparat eficiena clinic a edaravonei (Eda) i a edaravonei dexborneol (Eda.B) n tratamentul APCI.Au fost analizate retrospectiv datele clinice a 98 de pacieni, dintre care 48 au primit Eda i 50 Eda.B, intravenos, timp de dou sptmni.S-au evaluat parametrii hemoreologici, funciile neurologice i cognitive (NIHSS, MoCA, BI), markerii serici inflamatori i de stres oxidativ (IL-6, IL-17, IL-1, MMP-9, MDA, SOD, GSH-Px), precum i perfuzia cerebral pe baza RMN.Comparativ cu Eda, Eda.B a redus semnificativ vscozitatea sngelui i viteza de sedimentare a hematiilor, a mbuntit scorurile funcionale i a reglat favorabil markerii inflamatori i de stres oxidativ.De asemenea, Eda.B a crescut volumul i fluxul sanguin cerebral, reducnd timpul mediu de tranzit.Rata de eficien clinic a fost mai mare n grupul Eda.B (96,0% vs. 83,3%, p < 0,05), fr diferene semnificative n privina reaciilor adverse.n concluzie, Eda.B s-a dovedit mai eficient n ameliorarea funciilor neurologice i cognitive, a perfuziei cerebrale i n reducerea inflamaiei i stresului oxidativ la pacienii cu APCI.