ACE Report Cover
The Efficacy & Safety of Patient Controlled Intravenous Analgesia With Esketamine after THA
Language
Download
Cite
+ Favorites
Language
Download
Cite
+ Favorites
AceReport Image
ARTHROPLASTY
The Efficacy & Safety of Patient Controlled Intravenous Analgesia With Esketamine after THA .

The efficacy and safety of patient-controlled intravenous analgesia with esketamine after total hip arthroplasty: a randomized controlled trial.

BMC Anesthesiol. 2025 Jan 20;25(1):31.
Contributing Authors

S Qu WJ Zhang HJ Zhou F Deng RJ Liu WJ Yan

One hundred thirty-three patients undergoing elective total hip arthroplasty were randomized to receive either esketamine-based PCIA (n=44), sufentanil-based PCIA (n=45), or continuous fascia iliaca compartment block (FICB, n=44). The primary outcome was postoperative pain assessed via visual analogue scale (VAS) at rest and during movement. Secondary outcomes included pre- and postoperative anxiety and depression scores (SAS/SDS), patient and surgeon satisfaction, Harris hip function scores at 1 and 3 months, and the incidence of adverse reactions. Outcomes were assessed up to 3 months postoperatively. Overall, the results revealed that esketamine and FICB both provided superior pain control at 48 hours compared to sufentanil, with esketamine also showing better patient satisfaction and mood improvement. These findings suggest that esketamine PCIA is an effective and safer alternative for postoperative analgesia following hip arthroplasty.

Unlock the Full ACE Report

You have access to 4 more FREE articles this month.
Click below to unlock and view this ACE Reports
Unlock Now

Critical appraisals of the latest, high-impact randomized controlled trials and systematic reviews in orthopaedics

Access to OrthoEvidence podcast content, including collaborations with the Journal of Bone and Joint Surgery, interviews with internationally recognized surgeons, and roundtable discussions on orthopaedic news and topics

Subscription to The Pulse, a twice-weekly evidence-based newsletter designed to help you make better clinical decisions

Exclusive access to original content articles, including in-house systematic reviews, and articles on health research methods and hot orthopaedic topics

Or upgrade today and gain access to all OrthoEvidence
content for as little as $1.99 per week.
0 of 4 monthly FREE articles unlocked
You've reached your limit of 4 free articles views this month

Access to OrthoEvidence for as little as $1.99 per week.

Stay connected with latest evidence. Cancel at any time.
  • Critical appraisals of the latest, high-impact randomized controlled trials and systematic reviews in orthopaedics
  • Access to OrthoEvidence podcast content, including collaborations with the Journal of Bone and Joint Surgery, interviews with internationally recognized surgeons, and roundtable discussions on orthopaedic news and topics
  • Subscription to The Pulse, a twice-weekly evidence-based newsletter designed to help you make better clinical decisions
Upgrade
Welcome Back!
Forgot Password?
Start your FREE trial today!

Account will be affiliated with


OR
Forgot Password?

OR
Please check your email

If an account exists with the provided email address, a password reset email will be sent to you. If you don't see an email, please check your spam or junk folder.

For further assistance, contact our support team.

Translate ACE Report

OrthoEvidence utilizes a third-party translation service to make content accessible in multiple languages. Please note that while every effort is made to ensure accuracy, translations may not always be perfect.

Cite this ACE Report

OrthoEvidence. The Efficacy & Safety of Patient Controlled Intravenous Analgesia With Esketamine after THA. ACE Report. 2025;307(4):14. Available from: https://myorthoevidence.com/AceReport/Show/the-efficacy-safety-of-patient-controlled-intravenous-analgesia-with-esketamine-after-tha

Copy Citation
Please login to enable this feature

To access this feature, you must be logged into an active OrthoEvidence account. Please log in or create a FREE trial account.

Premium Member Feature

To access this feature, you must be logged into a premium OrthoEvidence account.

Share this ACE Report