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In light of the existing concerns on HES use, this study leaves several unanswered questions: how should patients be informed when they are asked to participate in a clinical trial that may randomise them to receive HES? How can a prestigious research group consider it appropriate to adopt a ’non‐inferiority’ study design to evaluate the safety profile of a controversial drug such as HES, when any proven beneficial effects (if there are any) remain unanswered?
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Ischemic Preconditioning Improves Cardiac Function in Off-pump CABG Patients
In patients undergoing off-pump coronary artery bypass grafting (CABG), regional ischemic preconditioning (IP) enhances postoperative myocardial performance, according to a recent report. […]
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Use of Cardiopulmonary Bypass for Treatment of Malignant Hyperthermia
This suggests the potential for CPB or extracorporeal membrane oxygenation (ECMO) as a possible treatment for the symptoms of MH.
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