Interpectoral and Pectoserratus Plane Block vs. Local Anesthetic Infiltration for Partial Mastectomy: A Prospective Randomized Trial

被引:0
|
作者
Eisler, Patryk [1 ,2 ]
Zimmermann, Stephan [1 ]
Henningsson, Ragnar [1 ]
机构
[1] Cent Hosp Karlstad, Dept Anesthes & Intens Care, Karlstad, Sweden
[2] Spital Grabs, Dept Anesthesia, Grabs, Switzerland
关键词
BREAST-CANCER SURGERY; PARAVERTEBRAL BLOCK; REGIONAL ANESTHESIA; ANALGESIA; CONSENSUS; RECOVERY; IMPACT; PAIN; CARE;
D O I
10.1155/2024/9989997
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background. Patients undergoing breast surgery are at risk of severe postoperative pain. Several opioid-sparing strategies exist to alleviate this condition. Regional anesthesia has long been a part of perioperative pain management for these patients. Aim. This randomized study examined the benefits of interpectoral and pectoserratus plane block (IPP/PSP), also known as pectoralis nerve plain block, compared with advanced local anesthetic infiltration. Methods. We analyzed 57 patients undergoing partial mastectomy with sentinel node dissection. They received either an ultrasound-guided IPP/PSP block performed preoperatively by an anesthetist or local anesthetic infiltration performed by the surgeon before and during the surgery. Results. Pain measured with the numerical rating scale (NRS) indicated no statistically significant difference between the groups (IPP/PSP 1.67 vs. infiltration 1.97; p value 0.578). Intraoperative use of fentanyl was significantly lower in the IPP/PSP group (0.18 mg vs 0.21 mg; p value 0.041). There was no statistically significant difference in the length of stay in the PACU (166 min vs 175 min; p value 0.51). There were no differences in reported postoperative nausea and vomiting (PONV) between the groups. The difference in postoperative use of oxycodone in the PACU (p value 0.7) and the use of oxycodone within 24 hours postoperatively (p value 0.87) was not statistically significant. Conclusions. Our study showed decreased intraoperative opioid use in the IPP/PSP group and no difference in postoperative pain scores up to 24 hours. Both groups reported low postoperative pain scores. This trial is registered with NCT04824599.
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页数:7
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