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- Publisher Website: 10.1186/s12871-020-01223-3
- Scopus: eid_2-s2.0-85098855945
- PMID: 33413104
- WOS: WOS:000609188800001
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Article: The analgesic efficacy of ultrasound-guided transversus abdominis plane (TAP) block combined with oral multimodal analgesia in comparison with oral multimodal analgesia after caesarean delivery: a randomized controlled trial
Title | The analgesic efficacy of ultrasound-guided transversus abdominis plane (TAP) block combined with oral multimodal analgesia in comparison with oral multimodal analgesia after caesarean delivery: a randomized controlled trial |
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Authors | |
Keywords | Transversus abdominis plane block Oral analgesics Caesarean deliver |
Issue Date | 2021 |
Publisher | BioMed Central Ltd. The Journal's web site is located at http://www.biomedcentral.com/bmcanesthesiol/ |
Citation | BMC Anesthesiology, 2021, v. 21, p. article no. 7 How to Cite? |
Abstract | Background:
The transversus abdominis plane (TAP) block is used increasingly in parturients after caesarean delivery. This is a randomized controlled trial to evaluate the effectiveness of bilateral single-shot of TAP blocks in patients who received multimodal oral analgesia for postoperative pain relief.
Methods:
Parturients who were scheduled for elective caesarean delivery under spinal anaesthesia were recruited and randomized to receive bilateral single-shot of TAP blocks or placebo in addition to multimodal oral analgesia which consisted of regular tramadol, celecoxib and paracetamol, with oral oxycodone used as a rescue for breakthrough pain. Only parturients in the TAP group would receive the TAP blocks with an injection of 15 ml (0.25%) ropivacaine on each side under aseptic techniques. All the parturients were evaluated for pain or related complications in the first 24 h after surgery. The primary outcome is the percentage of parturients who required oxycodone as a rescue analgesia.
Results:
Eighty and 79 parturients were allocated to the TAP and placebo group respectively. Nine out of 79 (11.4%) parturients in the TAP group and 15 out of 73 (20.5%) parturients in the placebo group required oxycodone for breakthrough pain, P = 0.122.
Conclusions:
Bilateral single-shot of TAP blocks confer little additional benefit when a multimodal oral analgesic regimen is used for pain control after caesarean section under spinal anaesthesia.
Trial registration:
Clinical Trial Registry of China (http://www.chictr.org.cn) identifier: ChiCTR-INR-16010130, retrospectively registered on Dec 12, 2016. |
Description | eid_2-s2.0-85098855945 |
Persistent Identifier | http://hdl.handle.net/10722/304483 |
ISSN | 2023 Impact Factor: 2.3 2023 SCImago Journal Rankings: 0.658 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | YU, Y | - |
dc.contributor.author | GAO, S | - |
dc.contributor.author | Yuen, VMY | - |
dc.contributor.author | Choi, SW | - |
dc.contributor.author | XU, X | - |
dc.date.accessioned | 2021-09-23T09:00:40Z | - |
dc.date.available | 2021-09-23T09:00:40Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | BMC Anesthesiology, 2021, v. 21, p. article no. 7 | - |
dc.identifier.issn | 1471-2253 | - |
dc.identifier.uri | http://hdl.handle.net/10722/304483 | - |
dc.description | eid_2-s2.0-85098855945 | - |
dc.description.abstract | Background: The transversus abdominis plane (TAP) block is used increasingly in parturients after caesarean delivery. This is a randomized controlled trial to evaluate the effectiveness of bilateral single-shot of TAP blocks in patients who received multimodal oral analgesia for postoperative pain relief. Methods: Parturients who were scheduled for elective caesarean delivery under spinal anaesthesia were recruited and randomized to receive bilateral single-shot of TAP blocks or placebo in addition to multimodal oral analgesia which consisted of regular tramadol, celecoxib and paracetamol, with oral oxycodone used as a rescue for breakthrough pain. Only parturients in the TAP group would receive the TAP blocks with an injection of 15 ml (0.25%) ropivacaine on each side under aseptic techniques. All the parturients were evaluated for pain or related complications in the first 24 h after surgery. The primary outcome is the percentage of parturients who required oxycodone as a rescue analgesia. Results: Eighty and 79 parturients were allocated to the TAP and placebo group respectively. Nine out of 79 (11.4%) parturients in the TAP group and 15 out of 73 (20.5%) parturients in the placebo group required oxycodone for breakthrough pain, P = 0.122. Conclusions: Bilateral single-shot of TAP blocks confer little additional benefit when a multimodal oral analgesic regimen is used for pain control after caesarean section under spinal anaesthesia. Trial registration: Clinical Trial Registry of China (http://www.chictr.org.cn) identifier: ChiCTR-INR-16010130, retrospectively registered on Dec 12, 2016. | - |
dc.language | eng | - |
dc.publisher | BioMed Central Ltd. The Journal's web site is located at http://www.biomedcentral.com/bmcanesthesiol/ | - |
dc.relation.ispartof | BMC Anesthesiology | - |
dc.rights | BMC Anesthesiology. Copyright © BioMed Central Ltd. | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Transversus abdominis plane block | - |
dc.subject | Oral analgesics | - |
dc.subject | Caesarean deliver | - |
dc.title | The analgesic efficacy of ultrasound-guided transversus abdominis plane (TAP) block combined with oral multimodal analgesia in comparison with oral multimodal analgesia after caesarean delivery: a randomized controlled trial | - |
dc.type | Article | - |
dc.identifier.email | Yuen, VMY: vtang131@hkucc.hku.hk | - |
dc.identifier.email | Choi, SW: htswchoi@HKUCC-COM.hku.hk | - |
dc.identifier.authority | Choi, SW=rp02552 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1186/s12871-020-01223-3 | - |
dc.identifier.pmid | 33413104 | - |
dc.identifier.pmcid | PMC7789306 | - |
dc.identifier.scopus | eid_2-s2.0-85098855945 | - |
dc.identifier.hkuros | 325344 | - |
dc.identifier.volume | 21 | - |
dc.identifier.spage | article no. 7 | - |
dc.identifier.epage | article no. 7 | - |
dc.identifier.isi | WOS:000609188800001 | - |
dc.publisher.place | United Kingdom | - |