PuraStat自组装肽水凝胶与矿物基血液喷雾用于猪上、下消化道病变内镜止血的比较

E. Gil, Kate M O'Neill, Elton Aleksi, J. Budrewicz, R. Melidone, L. Spirio
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摘要

目的比较基于rada16的自组装肽水凝胶与无机粉末喷雾装置对猪上、下消化道病变术后出血的控制效果。方法对6头约克郡猪在饲养第0天的胃和下结肠进行内镜下观察。3只动物的伤口用2.5% RADA16溶液(PuraStat®)治疗,2只动物用雾化矿物粉末(hemspray®)治疗,1只动物作为未治疗的对照组。主要结果是控制初始出血、止血时间和再出血发生率所需的试验品应用。次要结果包括动物恢复、每周内镜评估和4周研究结束时的临床病理。结果PuraStat组和止血喷雾组所需给药次数和止血时间相当。两种治疗的再出血率相当。在10分钟观察期的最后4分钟,12个止血喷雾组中有2个(17%)胃部位再出血,18个PuraStat组中没有一个(0%)胃部位再出血。在每周的内镜随访中未观察到迟发性出血。所有动物血液学和血清学指标均正常。组织学显示,PuraStat和血液喷雾剂治疗的所有缺陷都有预期的愈合反应,炎症比未治疗的部位少。不同组之间的胃和结肠的组织形态学观察具有可比性,用于测试和对照材料,炎症评分低于未治疗部位。两种系统的性能和可用性反应总体上都很好,尽管PuraStat在上消化道病变中治疗预期部位的能力评分明显更好。结论PuraStat和止血喷雾是治疗上、下消化道伤口轻、中度出血的有效止血剂。12个使用血液喷雾治疗的部位中2个出现再出血,18个使用purastat治疗的部位无再出血。与未治疗的对照组相比,PuraStat和hemspray与更好的伤口愈合相关。PuraStat与hemspray系统相比,治疗上消化道病变的能力更容易。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of PuraStat self-assembling peptide hydrogel versus mineral-based Hemospray for endoscopic hemostasis of upper and lower gastrointestinal lesions in pigs
Objective To compare a RADA16-based self-assembling peptide hydrogel versus an inorganic powder-based spray device for controlling postoperative bleeding in upper and lower GI mucosal lesions in pigs. Methods Multiple mucosal lesions were endoscopically-created in the stomachs and lower colons of six Yorkshire swine on Day 0. Three animals’ wounds were treated with 2.5% RADA16 solution (PuraStat®), two animals were treated with an aerosolized mineral powder (Hemospray®), and one animal was an untreated control. Primary outcomes were test article applications required to control initial bleeding, time-to-hemostasis, and rebleeding incidence. Secondary outcomes included animal recovery, and clinical pathology at weekly endoscopic evaluations and the 4-week study terminus. Results Number of material administrations required and time-to-hemostasis was comparable between PuraStat and Hemospray groups. Rebleeding rates were comparable between treatments. Two of 12 (17%) Hemospray and none of 18 (0%) PuraStat stomach sites experienced rebleeding during the final 4 min of the 10-min observation period. No delayed bleeding was observed during weekly endoscopic follow-ups. Hematology and serology values remained normal in all animals. Histology showed expected healing responses at all PuraStat- and Hemospray-treated defects, with less inflammation than untreated sites. Histomorphological observations were comparable between different groups for both the stomach and colon for test and control materials, with lower inflammation scores than untreated sites. Performance and usability responses were generally good with both systems, although the Ability to Treat Intended Site score was significantly better with PuraStat in upper GI lesions. Conclusions PuraStat and Hemospray were effective topical hemostats for mild-to-moderate bleeding in upper and lower GI wounds. Rebleeding was observed in two of 12 Hemospray-treated sites and none of 18 PuraStat-treated sites. PuraStat and Hemospray were associated with better wound healing than untreated controls. The ability to treat upper GI lesions was easier with the PuraStat versus Hemospray system.
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