Evidence map›Paper›PMID 38828388›Full record

ReviewFrontiers in pain research (Lausanne, Switzerland)2024

Mechanisms of complex regional pain syndrome.

Jagan Devarajan, Shayla Mena, Jianguo Cheng

Abstract readReview
In one paragraph

Review in Frontiers in pain research (Lausanne, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Mechanisms Underlying Pain Avoidance in Complex Regional Pain Syndrome.European journal of pain (London, England) · 2026
    Observational
  5. Review
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  11. Review
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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

3 authors.

Jagan DevarajanDepartment of Pain Management, Neurological Institute, Cleveland Clinic, Cleveland, OH, United States.
Shayla MenaDepartment of Pain Management, Neurological Institute, Cleveland Clinic, Cleveland, OH, United States.
Jianguo ChengDepartment of Pain Management and Neurosciences, Neurological Institute, Cleveland Clinic, Cleveland, OH, United States.

Funding

A first in class, mechanism-guided, cell-based therapy for complex regional pain syndromeUG3NS127258 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI CHENG, JIANGUO · 2022 to 2022
$2.0M
NINDS NIH HHS UG3 NS127258
6 · The paper itself

Abstract

Complex Regional Pain Syndrome (CRPS) is a chronic pain disorder characterized by a diverse array of symptoms, including pain that is disproportionate to the initial triggering event, accompanied by autonomic, sensory, motor, and sudomotor disturbances. The primary pathology of both types of CRPS (Type I, also known as reflex sympathetic dystrophy, RSD; Type II, also known as causalgia) is featured by allodynia, edema, changes in skin color and temperature, and dystrophy, predominantly affecting extremities. Recent studies started to unravel the complex pathogenic mechanisms of CRPS, particularly from an autoimmune and neuroimmune interaction perspective. CRPS is now recognized as a systemic disease that stems from a complex interplay of inflammatory, immunologic, neurogenic, genetic, and psychologic factors. The relative contributions of these factors may vary among patients and even within a single patient over time. Key mechanisms underlying clinical manifestations include peripheral and central sensitization, sympathetic dysregulation, and alterations in somatosensory processing. Enhanced understanding of the mechanisms of CRPS is crucial for the development of effective therapeutic interventions. While our mechanistic understanding of CRPS remains incomplete, this article updates recent research advancements and sheds light on the etiology, pathogenesis, and molecular underpinnings of CRPS.

Indexed as

autoimmune disorderautonomic dysfunctioncomplex regional pain syndromegenetic predispositionneuroimmune interactionsneuroinflammationpathophysiology

Identifiers

PMID38828388
PMCPMC11140106

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Registered trials

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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.