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Effectiveness of Fascia Iliaca Compartment Block after Elective Total Hip Replacement: A Prospective Randomized Controlled Study

机译:选修总髋关节替换后筋膜髂套房块的有效性:前瞻性随机对照研究

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摘要

Objective: An assessment of the feasibility of fascia iliaca compartment block (FICB) combined with nonopioid analgesics and patient controlled analgesia (PCA), oxycodone, in the perioperative anaesthetic management for elective total hip replacement (THR). Design: A randomised, single-center, open-label study. Setting: A single hospital. The study was conducted from October 2018 to May 2019. Participants: In total, 109 patients were scheduled for elective total hip replacement. Interventions: Postoperative FICB with 0.375% ropivacaine in conjunction with nonopioid analgesics (paracetamol, metamizole, and pregabalin) and oxycodone as rescue analgesia. Measurements: Pain intensity was measured using the Numeric Pain Rating Scale (NRS) at rest and during rehabilitation, the total dose of postoperative oxycodone required, the occurrence of opioid-related adverse events, patient hospitalisation time, and level of satisfaction. Follow-up period: 48 h. Main Results: A total of 109 patients were randomised into two groups and, of these, 9 were subsequently excluded from the analysis (three conversions to general anaesthesia, two failures to perform FICB, four failures to use the PCA pump). Patients in the FICB group received standard intravenous analgesia with FICB, and those in the control group were managed with standard intravenous analgesia only. Pain level measured with NRS was significantly lower at rest and during rehabilitation in the FICB group. Oxycodone use in the first 48 h was significantly higher in the control group (p < 0.001); additionally, the time to the first dose of rescue analgesia was significantly shorter (p < 0.001). In the control group, there was a higher rate of side effects and a significantly longer hospitalisation time (p < 0.001). Similarly, higher satisfaction with the applied analgesic treatment was noted in the FICB group. Conclusions: FICB in elective THR treatments is an effective form of analgesia, which reduces the need for opioids, the number of complications, the length of hospitalisation, and which ensures a high level of patient satisfaction with the analgesic treatment used. Trial registration: ClinicalTrials.gov No. {"type":"clinical-trial","attrs":{"text":"NCT04690647","term_id":"NCT04690647"}}NCT04690647.
机译:目的:评估筋膜室隔室块(FICB)与非磷镇痛和患者控制镇痛(PCA),羟考酮,在围手术期麻醉替代术(THR)中的围手术化麻醉剂(THR)中的可行性评估。设计:随机,单中心,开放标签学习。环境:单一医院。该研究于2018年10月至2019年5月进行。参与者:总共有109名患者进行选修总髋关节替代品。干预:术后FICB,0.375%Ropivacaine与非磷镇痛药(扑热息痛,Metamizole和Praetabalin)和羟考酮作为救援镇痛。测量:使用休息和康复期间的数值疼痛评定量表(NRS)测量疼痛强度,所需术后羟考酮的总剂量,阿片类药物相关不良事件,患者住院时间和满意度水平。随访期限:48小时。主要结果:总共109名患者随机分为两组,其中9例随后被排除在分析中(三次转换为全身麻醉,两个故障执行FICB,四次故障使用PCA泵)。 FICB组中的患者接受了具有FICB的标准静脉镇痛,但仅使用标准静脉镇痛进行控制组。在FICB组的休息和康复期间,用NRS测量的疼痛水平显着降低。在前48小时的羟考酮中使用对照组显着高(P <0.001);此外,第一剂量抢救镇痛的时间显着较短(P <0.001)。在对照组中,副作用率较高,住院时间明显更长(P <0.001)。类似地,在FICB组中注意到对应用镇痛治疗的更高满意度。结论:选择性Thr治疗的FICB是一种有效的镇痛形式,可降低阿片类药物,并发症的数量,住院时间,并确保使用所使用的镇痛治疗的患者满意度。试验注册:ClinicalTrials.gov No. {“类型”:“临床试验”,“attrs”:{“text”:“nct04690647”,“term_id”:“nct04690647”}} NCT04690647。

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