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Effectivity of dexamethasone in patients undergoing off-pump coronary artery bypass surgery
Based on our previous pilot study, systemic inflammatory response syndrome is more common in off-pump compared to on-pump coronary artery bypass. Therefore, we conducted a clinical trial of dexamethasone in patients undergoing off-pump coronary artery bypass. Sixty consecutive patients undergoing of...
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Published in: | Asian cardiovascular & thoracic annals 2021-06, Vol.29 (5), p.388-393 |
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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: | Based on our previous pilot study, systemic inflammatory response syndrome is more common in off-pump compared to on-pump coronary artery bypass. Therefore, we conducted a clinical trial of dexamethasone in patients undergoing off-pump coronary artery bypass.
Sixty consecutive patients undergoing off-pump coronary artery bypass were enrolled from August 2018 to January 2019 and randomized to a dexamethasone or placebo group of 30 each. Clinical outcomes were analyzed.
There was a lower incidence of major adverse cardiac events in the dexamethasone group compared to the placebo group (17% versus 43%,
= 0.024). Clinical outcomes in the dexamethasone group were better than those in the placebo group, in terms of duration of mechanical ventilation (
= 0.029), intensive care unit stay (
= 0.028), hospital stay (
= 0.04), and vasoactive-inotropic score (
= 0.045). There were significant differences in inflammatory markers between the two groups: interleukin-6 (
= 0.0001), procalcitonin (
= 0.0001), and C-reactive protein (
= 0.0001) were lower in the dexamethasone group. There was a significant association between the incidence of major adverse cardiac events and both interleukin-6 (
= 0.005) and procalcitonin (
= 0.007).
Preoperative dexamethasone in patients undergoing off-pump coronary artery bypass is effective in improving clinical outcomes and controlling the postoperative inflammatory reaction. |
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ISSN: | 0218-4923 1816-5370 |
DOI: | 10.1177/0218492320977648 |