Improving pain control during transarterial chemoembolization for hepatocellular carcinoma performed under local anesthesia with multimodal analgesia

被引:6
作者
Vanderbecq, Quentin
Gregory, Jules [1 ,2 ,3 ]
Dana, Jeremy
Burgio, Marco Dioguardi [1 ,2 ]
Garzelli, Lorenzo [1 ,2 ]
Raynaud, Lucas
Fremy, Sebastien [1 ]
Paulatto, Luisa
Bouattour, Mohamed [2 ,3 ]
Kavafyan-Lasserre, Juliette [4 ]
Vilgrain, Valerie [1 ,2 ]
Ronot, Maxime [1 ,2 ,5 ]
机构
[1] Hop Beaujon, AP HP Nord, Dept Radiol, F-92110 Clichy, France
[2] Univ Paris Cite, Ctr Rech Inflammat, INSERM U1149, CRI, F-75018 Paris, France
[3] FHU MOSA, F-92110 Clichy, France
[4] Hop Beaujon, AP HP Nord, Liver Canc Unit, F-92110 Clichy, France
[5] Hop Beaujon, AP HP Nord, Dept Anesthesiol & Intens Care, F-92110 Clichy, France
关键词
Analgesics opioid; Chemoembolization; Hepatocellular carcinoma; Liver cirrhosis; Non -narcotic analgesics; Pain measurement; PATIENT-CONTROLLED ANALGESIA; RANDOMIZED CONTROLLED-TRIAL; DRUG-ELUTING BEADS; POSTEMBOLIZATION SYNDROME; MORPHINE; TRAMADOL; EMBOLIZATION; DEXAMETHASONE; MANAGEMENT; NEFOPAM;
D O I
10.1016/j.diii.2022.10.013
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: The purpose of this study was to assess the performance of a reinforced analgesic protocol (RAP) on pain control in patients undergoing conventional trans-arterial chemoembolization (cTACE) for hepatocellu-lar carcinoma (HCC). Materials and methods: Eighty-one consecutive patients (57 men, 24 women) with a mean age of 69 + 10 (standard deviation) years (age range: 49-92 years) underwent 103 cTACEs. Standard antalgic protocol (50 mg hydroxyzine, 10 mg oxycodone, 8 mg ondansetron, and lidocaine for local anesthesia) was prospec-tively compared to a RAP (standard + 40 mg 2-h infusion nefopam and 50 mg tramadol). The individual pain risk was stratified based on age, the presence of cirrhosis and alcoholic liver disease, and patients were assigned to a low-risk group (standard protocol) or high-risk group (RAP). The primary endpoint was severe periprocedural abdominal pain (SAP), defined as a visual analog scale score >= 30/100. A predefined intermediate analysis was performed to monitor the benefit-risk of the RAP. Based on the intermediate analysis, all patients were treated with the RAP. Results: The intermediate analysis performed after 52 cTACE showed that 2/17 (12%) high-risk patients (i.e., those receiving the RAP) experienced SAP compared to 15/35 (43%) low-risk patients (odds ratio [OR] = 0.18; 95% confidence interval [CI]: 0.02-0.98; P = 0.03). Analysis of all procedures showed that 12/67 (18%) patients in cTACE receiving the RAP experienced SAP compared to 15/36 (42%) patients who did not receive it (OR = 3.27; 95% CI: 1.32-8.14; P = 0.01). There were no statistical differences in adverse events, particularly for nausea, between groups. Conclusion: Reinforcing the analgesic protocol by combining non-opioid and opioid molecules reduces peri-operative pain in patients undergoing cTACE for HCC.(c) 2022 Societe francaise de radiologie. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:123 / 132
页数:10
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