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丙泊酚全凭静脉麻醉的猪复苏后肠损伤及细菌易位时机的评估

Assessment of Post-Resuscitation Intestinal Injury and Timing of Bacterial Translocation in Swine Anaesthetized With Propofol-Based Total Intravenous Anaesthesia.

作者信息

Tassopoulos Andreas, Chalkias Athanasios, Papalois Apostolos, Karlovasiti Paraskevi, Zanda Jacopo Sergio Antonio, Chatzidakis Stefanos, Gazouli Maria, Iacovidou Nicoletta, Fanni Daniela, Xanthos Theodoros

机构信息

Department of Cardiology, Red Cross General Hospital, Athens, GRC.

Department of Anesthesiology, University of Thessaly, School of Health Sciences, Faculty of Medicine, Larisa, GRC.

出版信息

Cureus. 2020 Sep 10;12(9):e10362. doi: 10.7759/cureus.10362.

DOI:10.7759/cureus.10362
PMID:33062485
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7549874/
Abstract

Introduction and objectives Bacterial translocation (BT) is the passage of viable bacteria or endotoxins from the gastrointestinal lumen to extra-luminal tissues and is usually observed after intestinal ischaemia-reperfusion injury. The aim of this study was to investigate post-resuscitation BT after cardiac arrest and resuscitation in a swine anaesthetized with propofol-based total intravenous anaesthesia. Materials and methods Eighteen female Landrace/Large White piglets were randomly divided into control (CON), cardiac arrest (CA) and cardiac arrest-cardiopulmonary resuscitation (CA-CPR) groups. In the CON group, the animals were only monitored for two hours. In the CA group, the animals were not resuscitated and underwent necropsy immediately after cardiac arrest. In the CA-CPR group, the animals were resuscitated until the return of spontaneous circulation (ROSC) and were monitored for two hours. The animals of the CON and CA-CPR groups underwent necropsy 24 hours later. Bacterial translocation was assessed by blood and tissue cultures and endotoxin measurement in the portal and systemic circulation. Malondialdehyde content calculation and histological analysis of the intestine were performed in order to estimate ischemia and reperfusion (I/R) tissue damage. Results  Malondialdehyde content, an indicator of oxidative stress, was significantly higher in the CA-CPR group compared to the CA in homogenized ileum (p=0.016). Malondialdehyde content in homogenized colon revealed significantly higher levels in the CA-CPR group compared to the CON (p=0.004) and the CA group (p=0.016). We found significantly higher levels of portal endotoxin in the CA-CPR group compared to the CON (p=0.026) and the CA group (p=0.026). The number of positive mesenteric lymph nodes cultures for was greater in the CA-CPR group, followed by the CA and CON groups, although the difference was not significant (67%, 33%, and 33%, respectively; p=0.407). Conclusions Malondialdehyde content and portal endotoxin levels do not increase during the cardiac arrest interval, but only after CPR and ROSC. Although the number of positive MLNs cultures was greater in the CA-CPR animals, no statistically significant differences were observed between the three groups due to the short monitoring period.

摘要

引言与目的 细菌易位(BT)是指活细菌或内毒素从胃肠道腔转移至腔外组织,通常在肠道缺血再灌注损伤后出现。本研究旨在探讨在丙泊酚全静脉麻醉的猪心脏骤停及复苏后复苏期的细菌易位情况。

材料与方法 18只雌性长白/大白仔猪随机分为对照组(CON)、心脏骤停组(CA)和心脏骤停-心肺复苏组(CA-CPR)。CON组动物仅监测2小时。CA组动物不进行复苏,心脏骤停后立即进行尸检。CA-CPR组动物复苏至自主循环恢复(ROSC),并监测2小时。CON组和CA-CPR组动物24小时后进行尸检。通过血液和组织培养以及门静脉和体循环中的内毒素测量评估细菌易位。进行丙二醛含量计算和肠道组织学分析以评估缺血再灌注(I/R)组织损伤。

结果 氧化应激指标丙二醛含量在CA-CPR组匀浆回肠中显著高于CA组(p = 0.016)。CA-CPR组匀浆结肠中的丙二醛含量显著高于CON组(p = 0.004)和CA组(p = 0.016)。我们发现CA-CPR组门静脉内毒素水平显著高于CON组(p = 0.026)和CA组(p = 0.026)。CA-CPR组肠系膜淋巴结培养阳性的数量最多,其次是CA组和CON组,尽管差异不显著(分别为67%、33%和33%;p = 0.407)。

结论 丙二醛含量和门静脉内毒素水平在心脏骤停期间不增加,仅在心肺复苏和ROSC后增加。尽管CA-CPR组动物肠系膜淋巴结培养阳性数量较多,但由于监测期短,三组之间未观察到统计学显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ae4/7549874/5d82d9ba1ccd/cureus-0012-00000010362-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ae4/7549874/6fe97387aba3/cureus-0012-00000010362-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ae4/7549874/f54ad41d071f/cureus-0012-00000010362-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ae4/7549874/5d82d9ba1ccd/cureus-0012-00000010362-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ae4/7549874/6fe97387aba3/cureus-0012-00000010362-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ae4/7549874/f54ad41d071f/cureus-0012-00000010362-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ae4/7549874/5d82d9ba1ccd/cureus-0012-00000010362-i03.jpg

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