The Impact of Intraperitoneal Dexmedetomidine with Bupivacaine on Patients’ Postoperative Pain in Endometriosis Laparoscopic Surgery; A Randomized, Clinical Trial

In: Shiraz E-Medical Journal · 2019 · vol. 20(7) · doi:10.5812/semj.85296 · W2948661416
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Intraperitoneal dexmedetomidine plus bupivacaine significantly reduced postoperative pain scores and analgesic consumption in laparoscopic endometriosis surgery compared to bupivacaine alone.

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This randomized clinical trial compared intraperitoneal dexmedetomidine (DEX) plus bupivacaine versus bupivacaine alone and versus normal saline in patients undergoing laparoscopic surgery for endometriosis, assessing postoperative pain using VAS scores at multiple time points up to 48 hours and tracking rescue analgesic use. The DEX+bupivacaine group had significantly lower pain scores in the recovery room and at 2, 6, 12, 24, and 48 hours, with fewer rescue analgesic requirements, though the longest time to first rescue analgesia occurred in the bupivacaine-only group. The authors note limitations including a small sample size and that surgeries were not all performed by a single surgeon, despite efforts to unify surgical techniques and equipment. This paper is centrally about endometriosis — it tests intraperitoneal DEX plus bupivacaine for postoperative pain control after laparoscopic endometriosis surgery.

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Abstract

Background: Endometriosis is routinely treated with laparoscopy, which despite significant advantages over laparotomy cannot diminish postoperative pain. Insufficient postoperative pain control decreases patient satisfaction. Objectives: This study was designed to evaluate the efficacy of intraperitoneal dexmedetomidine (DEX) combined with bupivacaine on postoperative pain in endometriosis laparoscopic surgery. Methods: Fifty-three patients with endometriosis, scheduled for laparoscopy in Rasoul-e-Akram Hospital, Tehran, from January 2016 to May 2017 who were randomly divided into three groups, including group 1 (G1, n = 21) received 50 mL intraperitoneal saline, group 2 (G2, n = 16) received 50 mL intraperitoneal instillation of bupivacaine 0.25%, and group 3 (G3, n = 16) received 50 mL bupivacaine 0.25% plus dexmedetomidine 1 µg/kg. Each patient with a history of allergy to local anesthetics or dexmedetomidine, cardiac disease, renal or hepatic failure, severe pulmonary disease; in addition, pregnant and comorbid obese patients were excluded from the study. Patients’ postoperative pain was assessed in the recovery room after 2, 6, 12, 24, and 48 hours using visual analogue scale (VAS). Total analgesic consumption was also recorded. Results: The postoperative VAS scores were significantly lower in group 3 than other groups in the recovery room, and 2, 6, 12, 24 and 48 hours after the surgery (P < 0.001). However, there was no significant difference between 1 and 2 groups. Furthermore, total VAS in the first 24 hours in group 3 was significantly lower than the two other groups (P < 0.001). Conclusions: We conclude 1 μg/kg intraperitoneal DEX administration combined with bupivacaine may prolong postoperative analgesia and decrease rescue analgesia requirement compared with bupivacaine alone.
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The results of the present study on the assessment of postoperative VAS scores showed significantly less pain in group 3 (DEX + bupivacaine) than group 2 (bupivacaine) and group 1 (normal saline) in the recovery room, and 2, 6, 12, 24, and 48 hours after the surgery (P < 0.001) and fewer rescue analgesic requirement in group 3. While the longest time to the first rescue analgesic requirement was in group 2. As pain relief after gynecologic laparoscopic interventions has remained a critical issue, researchers broadly investigated to determine the highest safety and tolerance to analgesic techniques among patients who planned for surgery ( 20). Our study demonstrated that intraperitoneally distillated DEX with bupivacaine significantly attenuated postoperative pain and declined postoperative rescue analgesic consumption compared with intraperitoneally administered bupivacaine alone or normal saline. Meta-analysis studies on minor gynecologic procedures (such as tubal ligation) confirmed the efficacy of intraperitoneal bupivacaine on postoperative pain ( 21). However, research on patients undergoing minimally invasive gynecologic surgery has provided diverse results on the efficacy of intraperitoneal administration of bupivacaine on postoperative pain control. In this regard, Rivard et al. has found it efficient ( 19), while other researchers did not find any improvement in the pain control, narcotic use, length of hospital stay, or the level of patients’ satisfaction following the use of bupivacaine ( 22, 23), which is consistent with our study findings. It may also reflect this fact that intraperitoneal normal saline and intraperitoneal bupivacaine alone have similar effectiveness, as reported by Esmat and colleagues ( 6). As hypothesized, the local anesthetic agent administration causes visceral afferent signaling, and modification of visceral nociception that will block sodium channels ( 24). Thus recent studies have evaluated the efficacy of the combination of intraperitoneal bupivacaine with another local anesthetic agent. Ahmed et al. showed that intraperitoneal instillation of meperidine or DEX in combination with bupivacaine 0.25% significantly decreased the postoperative analgesic requirements and the incidence of shoulder pain compared with bupivacaine 0.25% alone in patients undergoing laparoscopic gynecological surgeries ( 25). Memis et al. also demonstrated that administrating a combination of clonidine and bupivacaine via intra-peritoneal root could provide more effective analgesia compared to bupivacaine alone during the early postoperative period ( 26). Narasimham and Rao also found that the intraperitoneal administration of bupivacaine alone or combined with DEX or tramadol could relieve procedure-related following after laparoscopic cholecystectomy ( 27). The prolonged sedation of DEX is attributed to its longer half-life than clonidine ( 28). The results of the above-mentioned studies are consistent with the results of the present study, confirming the efficacy of the combination of DEX with another analgesic; however, the surgical type and the adjuvant analgesic differ among studies. Similar to the results of the present study, other researchers have also revealed that intraperitoneal administration of DEX with bupivacaine, in laparoscopic gynecologic surgeries, was associated with a reduction in VAS and postoperative analgesic requirements in the hours of surgery ( 29- 31). In addition to these results, the present study showed maximum painlessness at 48th hour postoperatively in DEX plus bupivacaine group. Additionally, there was no statistically significant difference in the place of maximum pain in 24 hours and administration of local anesthetic had no efficiency on trocar site pain. As far as the authors are concerned, the combination of DEX with bupivacaine has not been studied on the laparoscopic procedure for the treatment of endometriosis and the origin of postoperative pain depends on the surgical technique. Therefore, further studies on the pain origin of this specific type of surgery may elucidate the mode of analgesia in the present study. The strengthening point of the present study was comprised of a combination of gynecologic procedures such as retroperitoneal dissection, endometrioma, endometriotic nodule resection, and hysterectomy; all patients were postoperatively planned for similar pain regimen, suggesting the differences in pain controlling due to administrating intra-peritoneal local anesthetics. Also, the extended follow-up period of 48 hours (compared to 24 hours in previous studies) is the other strength of our study. The limitation of our study included small sample size and all surgeries were not performed by a single surgeon; however, the surgical techniques and equipment were unified. As there are few studies on using a combination of DEX and bupivacaine, further studies considering different dosages and roots of local anesthetics are required to compare this approach of analgesia with other regional techniques with the goal of achieving more benefit with regard to postoperative pain relief along with minimized adverse effects following laparoscopic surgeries.

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Outcome instruments

VAS-pain

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endometriosis

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