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Perioperative erythropoietin protects the CNS against ischemic lesions in patients after open heart surgery
Summary Aim The aim of this study was to establish erythropoietin as a protective factor against brain ischemia during open heart surgery. Methods A total of 36 consecutive patients scheduled for revascularization heart surgery were included in the study. Of the patients 18 received 3 intravenous do...
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Published in: | Wiener Klinische Wochenschrift 2016-12, Vol.128 (23-24), p.875-881 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Summary
Aim
The aim of this study was to establish erythropoietin as a protective factor against brain ischemia during open heart surgery.
Methods
A total of 36 consecutive patients scheduled for revascularization heart surgery were included in the study. Of the patients 18 received 3 intravenous doses of recombinant human erythropoietin (rHuEpo, 24,000 IU) and 18 patients received a placebo. Magnetic resonance imaging (MRI) to detect new brain ischemic lesions was performed. Additionally, S100A, S100B, neuron-specific enolase A and B (NSE-A and B) and the concentration of antibodies against N‑methyl-D-aspartate receptors (NMDAR) to identify new neurological complications were determined.
Results
Patients who received rHuEpo showed no postoperative ischemic changes in the brain on MRI images. In the control group 5 (27.8 %) new ischemic lesions were found. The NMDAR antibody concentration, S100A, S100B and NSE showed no significant differences between the groups for new cerebral ischemia. High levels of lactate before and after external aortic compression (
p
= 0.022 and
p
= 0.048, respectively) and duration of operation could predict new ischemic lesions (
p
= 0.009).
Conclusions
The addition of rHuEpo reduced the formation of lesions detectable by MRI in the brain and could be used clinically as neuroprotection in cardiac surgery. |
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ISSN: | 0043-5325 1613-7671 |
DOI: | 10.1007/s00508-016-1063-0 |