E. Upryamova, E. Shifman, V. Krasnopolskiy, Ovezov Am
{"title":"计划性间歇硬膜外注射(PIEB)缓解分娩疼痛","authors":"E. Upryamova, E. Shifman, V. Krasnopolskiy, Ovezov Am","doi":"10.17116/anaesthesiology202004169","DOIUrl":null,"url":null,"abstract":"Objective. To evaluate an effectiveness of the available modes of epidural analgesia (bolus, patient-controlled epidural analgesia, patient-controlled epidural analgesia combined with continuous epidural infusion, programmed intermittent epidural bolus combined with patient-controlled epidural analgesia) in parallel with a stepwise decrease in levobupivacaine concentration for analysis of optimal ratio «mode — concentration of anesthetic» in labor pain relief. Material and methods. We studied 145 women. The onset of pain relief was determined by regular labor. All women were divided into 5 groups depending on the mode of pain relief and local anesthetic concentration: on-demand manual boluses, patientcontrolled epidural analgesia (PCEA), patient-controlled epidural analgesia combined with continuous epidural infusion (PCEA + CEI), programmed intermittent epidural bolus combined with patient-controlled epidural analgesia (PIEB + PCEA); levobupivacaine 0.25 mg/ml; 1.25 mg/ml; 0.625 mg/ml. Labor pain relief efficacy was evaluated using a visual analogue scale. The time points for recording the values were as follows: before anesthesia, after 15 minutes from anesthesia onset, every 30 minutes until the uterine cervix is completely opened and during labor contractions at the delivery room. Анестезиология и реаниматология","PeriodicalId":297480,"journal":{"name":"Anesteziologiya i reanimatologiya","volume":"19 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Programmed intermittent epidural bolus (PIEB) for labor pain relief\",\"authors\":\"E. Upryamova, E. Shifman, V. Krasnopolskiy, Ovezov Am\",\"doi\":\"10.17116/anaesthesiology202004169\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective. To evaluate an effectiveness of the available modes of epidural analgesia (bolus, patient-controlled epidural analgesia, patient-controlled epidural analgesia combined with continuous epidural infusion, programmed intermittent epidural bolus combined with patient-controlled epidural analgesia) in parallel with a stepwise decrease in levobupivacaine concentration for analysis of optimal ratio «mode — concentration of anesthetic» in labor pain relief. Material and methods. We studied 145 women. The onset of pain relief was determined by regular labor. All women were divided into 5 groups depending on the mode of pain relief and local anesthetic concentration: on-demand manual boluses, patientcontrolled epidural analgesia (PCEA), patient-controlled epidural analgesia combined with continuous epidural infusion (PCEA + CEI), programmed intermittent epidural bolus combined with patient-controlled epidural analgesia (PIEB + PCEA); levobupivacaine 0.25 mg/ml; 1.25 mg/ml; 0.625 mg/ml. Labor pain relief efficacy was evaluated using a visual analogue scale. The time points for recording the values were as follows: before anesthesia, after 15 minutes from anesthesia onset, every 30 minutes until the uterine cervix is completely opened and during labor contractions at the delivery room. Анестезиология и реаниматология\",\"PeriodicalId\":297480,\"journal\":{\"name\":\"Anesteziologiya i reanimatologiya\",\"volume\":\"19 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Anesteziologiya i reanimatologiya\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.17116/anaesthesiology202004169\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Anesteziologiya i reanimatologiya","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17116/anaesthesiology202004169","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Programmed intermittent epidural bolus (PIEB) for labor pain relief
Objective. To evaluate an effectiveness of the available modes of epidural analgesia (bolus, patient-controlled epidural analgesia, patient-controlled epidural analgesia combined with continuous epidural infusion, programmed intermittent epidural bolus combined with patient-controlled epidural analgesia) in parallel with a stepwise decrease in levobupivacaine concentration for analysis of optimal ratio «mode — concentration of anesthetic» in labor pain relief. Material and methods. We studied 145 women. The onset of pain relief was determined by regular labor. All women were divided into 5 groups depending on the mode of pain relief and local anesthetic concentration: on-demand manual boluses, patientcontrolled epidural analgesia (PCEA), patient-controlled epidural analgesia combined with continuous epidural infusion (PCEA + CEI), programmed intermittent epidural bolus combined with patient-controlled epidural analgesia (PIEB + PCEA); levobupivacaine 0.25 mg/ml; 1.25 mg/ml; 0.625 mg/ml. Labor pain relief efficacy was evaluated using a visual analogue scale. The time points for recording the values were as follows: before anesthesia, after 15 minutes from anesthesia onset, every 30 minutes until the uterine cervix is completely opened and during labor contractions at the delivery room. Анестезиология и реаниматология