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Authors Hu J, Huang D, Li M, Wu C, Zhang J
Received 11 April 2018
Accepted for publication 25 July 2018
Published 2 November 2018 Volume 2018:11 Pages 2633—2643
DOI https://doi.org/10.2147/JPR.S170810
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Amy Norman
Peer reviewer comments 2
Editor who approved publication: Dr E Alfonso Romero-Sandoval
Background: Pregabalin (PGB) and gabapentin (GBP) are current and emerging
drugs in the field of pre-emptive preoperative analgesia. However, the role of
PGB or GBP in acute postoperative pain management still remains elusive.
Materials and
methods: We conducted a comprehensive
literature search of articles published by December 3, 2017. A total of 79
randomized controlled trials with 6,201 patients receiving single-dose
premedication were included. Through a network meta-analysis (NMA), we
validated the analgesic effect and incidence of adverse events by using various
doses of PGB or GBP administration.
Results: NMA results suggested that the analgesic effect may be dose related.
For 24-hour opioid consumption, a consistent decrease was found with the
increase in the dose of PGB or GBP. For 24-hour pain score at rest, a high dose
(≥150 mg) of PGB was more effective in decreasing pain score than a dose of 75
mg, and a high dose (≥900 mg) of GBP reduced pain intensity than doses of 300
or 600 mg. Moreover, the incidence of adverse reactions varied with varying
doses of PGB or GBP.
Conclusion: A dose–response relationship was detected in opioid consumption
and postoperative pain for a single-dose preoperative administration of PGB and
GBP. Making reasonable choice of drugs and dosage may prevent the occurrence of
adverse reactions.
Keywords: PGB, GBP, single dose, acute postoperative pain, network meta-analysis
