Evidence map›Paper›PMID 35688442›Full record

Trial reportThe journal of knee surgery2023

HTX-011 in Combination with Multimodal Analgesic Regimen Minimized Severe Pain and Opioid Use after Total Knee Arthroplasty in an Open-Label Study.

Gwo-Chin Lee, Richard Berkowitz, Scott Hacker, Jia Hu, Alan Rechter

2 registry-linked trialsOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The journal of knee surgery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03974932 phase3completednot on this map

A Phase 3b, Open-Label Study of HTX-011 as Part of a Scheduled Non-Opioid Multimodal Analgesic Regimen in Subjects Undergoing Total Knee Arthroplasty

TypeinterventionalSponsorHeron TherapeuticsRan2019 to 2021Enrolled116ConditionsAnalgesiaArmsHTX-011, Ibuprofen, Acetaminophen, Celecoxib, +/- Bupivacaine HCl
NCT07775248 phase4recruitingnot on this mapstarted 2025, after this paper: background citation

Novel Extended-Release Bupivacaine Polymer for Sustained Pain Relief Following Total Knee Arthroplasty

TypeinterventionalSponsorHenry Ford Health SystemRan2025 to 2026Enrolled150ConditionsOsteoarthritis (OA) of the KneeArmsPeriarticular Injection, Adductor Canal Block, Bupivacaine-Meloxicam
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

Gwo-Chin LeeDepartment of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, Pennsylvania.
Richard BerkowitzUniversity Orthopedic and Joint Replacement Center, Tamarac, Florida.
Scott HackerGrossmont Orthopedic Medical Group, La Mesa, California.
Jia HuHeron Therapeutics, Inc., San Diego, California.
Alan RechterDepartment of Orthopaedic Surgery, Orthopaedic Associates, LLP, Houston, Texas.
Heron Therapeutics (United States) · USHouston Perinatal Associates · USSharp Grossmont Hospital · USUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Total knee arthroplasty (TKA) can be associated with significant postoperative pain despite multimodal analgesic (MMA) protocols, and most patients require the use of opioids postoperatively. HTX-011 is a dual-acting local anesthetic containing bupivacaine and low-dose meloxicam in an extended-release polymer. In a prior randomized controlled trial (RCT), HTX-011 reduced pain and opioid use through 72 hours after TKA compared with bupivacaine hydrochloride. This open-label study (NCT03974932) evaluated the efficacy and safety of HTX-011 combined with an MMA regimen in patients undergoing TKA under spinal anesthesia. All patients received intraoperative HTX-011 (400 mg bupivacaine/12 mg meloxicam) in combination with an MMA regimen consisting of preoperative acetaminophen, celecoxib, and pregabalin and postoperative acetaminophen and celecoxib until discharge. Opioid rescue was allowed upon patient request for additional pain control. Pain scores, opioid consumption, discharge readiness, and adverse events were recorded. Fifty-one patients were treated. Compared with the prior RCT, HTX-011 with this MMA regimen further lowered pain scores and reduced opioid use. Mean patient-reported pain scores remained in the mild range, and 82% of patients or more did not experience severe pain at any individual time point through 72 hours after surgery. Mean total opioid consumption was low over 72 hours: 24.8 morphine milligram equivalents (1-2 tablets of oxycodone 10 mg/day). Approximately 60% of patients were ready for discharge by 12 hours, and 39% were discharged without an opioid prescription and did not call back for pain management. The treatment regimen was well tolerated, and no added risk was observed with the addition of MMA. HTX-011 with an MMA regimen reduced postoperative pain and opioid use following TKA.

Indexed as

Arthroplasty, Replacement, KneeOpioid-Related DisordersAcetaminophenAnalgesicsAnalgesics, OpioidAnesthetics, LocalBupivacaineCelecoxibHumansMeloxicamPostoperative PainAcetaminophenAnalgesicsAnalgesics, OpioidAnesthetics, LocalBupivacaineCelecoxibMeloxicam

Identifiers

PMID35688442
PMCPMC10289832
OpenAlexW4281733214

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.