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Published on: January 21, 2020
Leukocytes in Complex Regional Pain Syndrome type I
Edward C T H Tan1, Wim J G Oyen, R Jan A Goris
1Department of General Surgery - Section Traumatology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands. E.Tan@chir.umcn.nl
Insights
This study found increased leukocyte accumulation in patients with Complex Regional Pain Syndrome type I (CRPS I), suggesting a role for these white blood cells in the condition's development.
Area of Science:
- Pain Medicine
- Immunology
- Radiology
Background:
- The exact cause of Complex Regional Pain Syndrome type I (CRPS I) remains unknown.
- Inflammation is suspected to be a key factor in CRPS I development.
- Leukocytes (white blood cells) may contribute to the inflammatory process in CRPS I.
Purpose of the Study:
- To investigate the role of leukocytes in the pathophysiology of acute CRPS I.
- To assess leukocyte accumulation in patients with CRPS I using radiolabeled leukocyte scans.
Main Methods:
- A pilot study involving six patients diagnosed with acute warm CRPS I.
- Radiolabeled autologous leukocyte scans were performed on both hands of CRPS I patients.
- Comparison was made with unaffected limbs and three control patients with Colles fracture but no CRPS I.
Main Results:
- Leukocyte accumulation was significantly higher in the affected limbs of CRPS I patients compared to controls (mean ratio 1.49 vs. 1.09 at 4 hours post-injection).
- Asymmetrical leukocyte accumulation was observed in CRPS I patients, but not in controls.
- A statistically significant difference (p=0.012) in leukocyte accumulation was found between CRPS I patients and controls at 4 hours.
Conclusions:
- This study provides the first evidence suggesting a significant increase in leukocyte accumulation in acute CRPS I.
- Leukocytes appear to play a role in the underlying pathophysiology of CRPS I.
Objective:
The pathophysiology of Complex Regional Pain Syndrome type I (CRPS I) is unclear. An inflammatory reaction may cause the syndrome in which leukocytes may play an important role.
Materials And Methods:
In this pilot study of six patients with acute warm CRPS I, we performed radiolabeled autologous leukocyte scans of both hands, in order to assess leukocyte accumulation. Comparison was made with the unaffected limb, and with three control patients with a Colles fracture without CRPS I.
Results:
Images of the CRPS I patients obtained 4 h after leukocyte injection provided the clearest results. At 4 h post-injection, there was clear, asymmetrical leukocyte accumulation in the affected extremity with a mean ratio of 1.49+/-0.19. In control patients, no asymmetry was observed between hands (mean ratio 1.09+/-0.06), indicating the absence of specific leukocyte accumulation. There was a statistically significant difference between CRPS I and control subjects 4 h post injection (p=0.012).
Conclusion:
We found a significantly increased accumulation of leukocytes in patients with CRPS I. This is the first study to show a possible role for leukocytes in the pathophysiology of acute CRPS I.
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