Off-label Rescue Agents for Vasoplegic Syndrome after Cardiopulmonary Bypass

Abstract

Abstract

Introduction: Cardiovascular disease is the number one cause of death in the United States today¹. Cardiopulmonary bypass (CPB) is a common technique used in the surgical management of cardiovascular disease. A relatively common complication of CPB is vasoplegia, which has an approximate incidence of anywhere from 5-25%^1-8. Methylene blue is used to treat vasoplegic syndrome (VS) when higher dose vasopressors are ineffective. Vasoplegic syndrome (VS) is defined as a syndrome of low systemic vascular resistance (SVR) in the presence of normal or high cardiac output^1-4. Generally, VS is characterized as a high cardiac output state (CI < 2.2 L/min/m²) with difficulty maintaining a mean arterial pressure (MAP) greater than 60 mmHg despite increasing vasopressor requirements^1-3,7. The focus of this case report is to examine methylene blue’s effectiveness in treating vasoplegia after weaning from CPB. This case report will also compare and contrast methylene blue and another rescue agent, hydroxocobalamin, and how they combat vasoplegia.

Case presentation: The case involved a 65-year-old male presenting for an aortic root and aortic valve replacement and removal of an abscess in his heart. The patient was under general anesthesia, put on cardiopulmonary bypass and then underwent a deep hypothermic circulatory arrest for the placement of the aortic root graft and aortic valve. Weaning from bypass was difficult as a result of vasoplegia, for which methylene blue was given when vasopressor requirements were increasing.  

Discussion: Methylene blue is a guanylyl cyclase inhibitor that has been found to increase SVR and decrease vasopressor requirements in vasoplegic syndrome by inhibiting nitric oxide synthase (NOS), thus limiting the production of nitric oxide (NO) as well as inhibiting the enzyme guanylyl cyclase and preventing vasodilation⁵. The timing of administration of methylene blue is debatable, being that it is commonly given postoperatively, but the literature favors earlier administration in high-risk patients that will be placed on CPB^2-5. Typical dosing for methylene blue is 2 mg/kg intravenously (IV) but increasing the dose to 3 mg/kg can be used to account for the larger volume of distribution (Vd) that is present in patients on CPB². The only true contraindications for methylene blue are a hypersensitivity to the drug and a deficiency in the glucose-6-phosphate dehydrogenase, which is the enzyme that is responsible for turning methylene blue into its metabolites^1-8. Treating VS with methylene blue after CPB has shown significantly quicker recovery and normal hemodynamics, shorter duration of vasopressor infusions, less incidence of renal complications, shorter length of stay (LOS) and less 30-day mortality⁶. 

References:

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