Literature DB >> 32481441

The 95% effective dose of nalbuphine in patient-controlled intravenous analgesia for patients undergoing laparoscopic total hysterectomy compared to equivalent sufentanil.

Zhentao Sun1, Zefei Zhu, Guanyu Yang, Hongyu Zheng.   

Abstract

PURPOSE: To evaluate the 95% effective dose of nalbuphine in patient-controlled intravenous analgesia (PCIA) by the sequential method and compare the analgesia efficacy with the equivalent dose of sufentanil on patients undergoing laparoscopic total hysterectomy.
METHODS: In the first part, we defined a successful analgesia as the highest VAS ≤3 in 24 hours postoperatively. On the contrary, a failed analgesia was the highest VAS>3. According to the last patient's outcome, the next patients would be given an increase or decreased dose grade. This process ended up with 9 cross-over points. In the second part, 60 patients undergoing laparoscopic total hysterectomy were selected. They were randomly divided into 2 groups (n = 30 each group): receiving sufentanil 1.78 μg/kg (group S) and nalbuphine 1.78 mg/kg (group N). PCIA pump was given at the end of the operation with 5 mL bonus loading. The total amount of PCIA was 100 mL and programmed to deliver 0.5 mL each time with a lockout interval of 15 minutes and the background infusion amount of 2 mL/h. The VAS score and Ramsay score of were collected after the operation, the number of effective pressing times of PCIA were also recorded. Adverse reactions were documented in detail.
RESULTS: The 95% effective dose of nalbuphine in PCIA on patients undergoing laparoscopic total hysterectomy was 1.78 mg/kg. There was no significant difference in VAS between the sufentanil group and the nalbuphine groups (P > .05), but the number of the use of PCIA in the group S was more than that in the group N obviously (P <.05). The group S has a lower ramsay sedation score than group N at every time point. (P <.05). The incidence of nausea and vomiting was not statistically significant differences between two groups in the first 24 hours after colonoscopy (P >  q .05).
CONCLUSION: Nalbuphine 1.78 mg/kg in PCIA is recommended for the patients undergoing laparoscopic total hysterectomy. And nalbuphine is a reasonable alternative to sufentanil when used in PCIA.

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Year:  2020        PMID: 32481441      PMCID: PMC9452073          DOI: 10.1097/MD.0000000000020424

Source DB:  PubMed          Journal:  Medicine (Baltimore)        ISSN: 0025-7974            Impact factor:   1.817


  7 in total

1.  A Dose-Response Relationship Study of Prophylactic Nalbuphine to Reduce Pain During the Awakening Period in Patients Undergoing Laparoscopic Total Hysterectomy: A Randomized, Controlled, Double-Blind Clinical Study.

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Journal:  Drug Des Devel Ther       Date:  2022-03-31       Impact factor: 4.162

2.  The 95% effective dose of nalbuphine in patient-controlled intravenous analgesia for patients undergoing laparoscopic total hysterectomy compared to equivalent sufentanil: Retraction.

Authors: 
Journal:  Medicine (Baltimore)       Date:  2022-06-17       Impact factor: 1.817

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4.  Analgesic Effect Comparison Between Nalbuphine and Sufentanil for Patient-Controlled Intravenous Analgesia After Cesarean Section.

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Journal:  Front Pharmacol       Date:  2020-11-16       Impact factor: 5.810

5.  Analgesic Effects of Different κ-Receptor Agonists Used in Daytime Laparoscopic Cholecystectomy.

Authors:  Wanjun Zhou; Jiawu Wang; Chengyun Hu; Feibiao Dai; Zhetao Zhang; Chuanyao Li; Chaoliang Tang; Yanhu Xie
Journal:  Biomed Res Int       Date:  2021-12-29       Impact factor: 3.411

6.  Comparison of Analgesic Effects between Nalbuphine and Sufentanil in First-Trimester Surgical Abortion: A Randomized, Double-Blind, Controlled Trial.

Authors:  Panpan Fang; Jing Qian; Jianming Ding; Xiao Pan; Han Su; Xuesheng Liu
Journal:  Pain Ther       Date:  2021-11-29

7.  Application of Ultrasound-Guided Transversus Abdominis Plane Block Combined with Nalbuphine Patient-Controlled Intravenous Analgesia in Postoperative Analgesia After Laparotomy: A Randomized Controlled Trial.

Authors:  Kunyu Han; Yuhe Zhang; Ruiping Bai; Rui An; Simei Zhang; Mengwen Xue; Xin Shen
Journal:  Pain Ther       Date:  2022-04-14
  7 in total

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