Evidence map›Paper›PMID 41169900›Full record

ReviewJournal of pain research2025

Chemonucleolysis for Lumbar Disc Herniation: History and Current State of the Technology.

Timothy R Deer, Kevin E Macadaeg, Kee D Kim, David J Copenhaver, Boyle C Cheng, Anand Patel, Alexander Vaccaro, Kenneth D Candido, Pragya B Gupta, Douglas P Beall

Abstract readReview
In one paragraph

Review in Journal of pain research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. [Lumbar disc herniation].Orthopadie (Heidelberg, Germany) · 2026
    Review
  3. Article
  4. Review
  5. Article
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

10 authors.

Timothy R Deer *Department of Pain Management, The Spine and Nerve Center of the Virginias, Charleston, WV, USA.ORCID 0000-0001-8907-7730
Kevin E Macadaeg *Department of Anesthesiology and Pain Management, Indiana Spine Group, Carmel, IN, USA.
Kee D KimDepartment of Spinal Neurosurgery, University of California, Davis, Department of Neurological Surgery, Sacramento, CA, USA.
David J CopenhaverDepartment of Anesthesiology and Pain Medicine, University of California, Davis, Sacramento, CA, USA.
Boyle C ChengDepartment of Neurosurgery, Allegheny Health Network Research Institute, Pittsburgh, PA, USA.ORCID 0000-0002-1725-5515
Anand PatelDepartment of Orthopedics, Conquest Research, Winter Park, FL, USA.
Alexander VaccaroDepartment of Orthopaedic Surgery, Rothman Orthopaedic Institute, Philadelphia, PA, USA.
Kenneth D CandidoDepartment of Pain Management, Chicago Anesthesia Pain Specialists, Chicago, IL, USA.
Pragya B GuptaDepartment of Interventional Pain Medicine, Otrimed Clinical Research, Edgewood, KY, USA.ORCID 0000-0002-2482-7569
Douglas P BeallDepartment of Pain Management, Comprehensive Specialty Care, Edmond, OK, USA.ORCID 0000-0001-8340-696X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The most common cause of radicular leg pain is lumbar disc herniation (LDH). LDH occurs when the central disc material, predominantly the nucleus pulposus, is displaced beyond the margins of the disc, compressing the spinal nerve roots and in turn causing radicular leg pain. Patients with persistent LDH symptoms that do not respond to conservative management have limited treatment options other than surgery. There has been a resurgence of interest in chemonucleolysis, in which an enzyme or other substance is directly injected into the intervertebral disc with the goal of reducing the size of the nucleus pulposus, relieving pressure on the nerve roots. Chemonucleolysis with chymopapain was widely used in the 1980s and 1990s as an effective treatment for LDH that was less invasive than surgery. Following the discontinuation of chymopapain in 1999, no chemonucleolytic therapy has been commercially available in the US. SI-6603 (condoliase) is a mucopolysaccharidase that selectively degrades chondroitin sulfate glycosaminoglycan (GAG) chains in the nucleus pulposus. Condoliase is approved in Japan and recently demonstrated significant improvements in worst leg pain (vs sham) in a pivotal US phase 3 clinical trial. Chemonucleolytic agents with less substrate specificity include gelified ethanol and oxygen-ozone, which are under postmarket surveillance in Europe, as well as collagenase in China. The re-emergence of chemonucleolysis is anticipated to improve the treatment landscape for LDH, providing patients with the option to avoid more invasive surgical intervention.

Indexed as

condoliaseintradiscal therapylumbar radiculopathyradicular leg painSI-6603

Identifiers

PMID41169900
PMCPMC12570984

What OpenQuestion holds

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Registered trials

None linked

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.