Short‐Term Glucocorticoid Treatment Normalizes the Microcirculatory Response to Remote Ischemic Conditioning in Early Complex Regional Pain Syndrome

• Published in: Pain practice Vol. 19; no. 2; pp. 168 - 175
• Main Authors: Kumowski, Nina, Hegelmaier, Tobias, Kolbenschlag, Jonas, Mainka, Tina, Michel‐Lauter, Beate, Maier, Christoph
• Format: Journal Article
• Language: English
• Published: United States 01.02.2019
• Subjects: complex regional pain syndromes; glucocorticoids; inflammation; microcirculation; remote ischemic conditioning; complex regional pain syndromes; remote ischemic conditioning; glucocorticoids; inflammation; microcirculation
• ISSN: 1530-7085; 1533-2500
• DOI: 10.1111/papr.12730

Background The early phase of complex regional pain syndrome (CRPS) is characterized by an inflammatory state and therefore often treated with anti‐inflammatory acting glucocorticoids. Recently, we demonstrated that remote ischemic conditioning (RIC), a cyclic application of nondamaging ischemia on a remote extremity, reduces blood flow and increases oxygen extraction in the CRPS‐affected extremity. Aim The aim of the presented study was to analyze the effect of short‐term pain treatment including glucocorticoid pulse treatment on the RIC‐induced perfusion parameters. Method Independently from the study, pain treatment was started with an oral glucocorticoid pulse (180 to 360 mg prednisolone) in 12 patients with CRPS (disease duration < 1 year). RIC was conducted before and after pulse treatment. Three cycles of 5 minutes ischemia and 10 minutes reperfusion were applied to the contralateral limb. Blood flow, tissue oxygenation, and oxygen extraction fraction were assessed ipsilateral before and during RIC. Current pain was assessed on the numeric rating scale (0 to 10), and finger–palm distance was measured. Results Pain level (5.8 ± 1.5 vs. 3.1 ± 1.1) and finger–palm distance (5 ± 1.9 cm vs. 3.7 ± 1.9 cm) were decreased significantly by the treatment. RIC decreased blood flow by 32.8% ± 42.8% (P < 0.05) and increased oxygen extraction fraction by 8.5% ± 10.3% (P < 0.05) solely before the treatment. After treatment, all parameters remained unchanged after RIC (P < 0.05 vs. before), comparable to healthy subjects. Conclusion Confirming previous results, RIC presumably unmasks luxury perfusion in untreated CRPS patients. In accordance with the clinical improvement, the short‐term pain treatment with glucocorticoids as major component normalizes impaired perfusion. These results might underline the rationale for anti‐inflammatory treatment in early‐phase CRPS.