Abstract

IntroductionThere are many reasons to believe that the nitric oxide/guanosine 3’5’ - cyclic monophosphate (or NO/cGMP) pathway on vasoplegic states is underestimated. To study indigo carmine (IC) as an alternative to methylene blue was the investigation rationale.MethodsThe IC (3mg/kg intravenous infusion) study protocol included five experimental groups; 1) Control group — saline was injected at 0 and 10 minutes; 2) IC group — IC was injected at 0 and saline at 10 minutes; 3) compound 48/80 (C48/80) group — C48/80 was injected at 0 minute and saline at 10 minutes; 4) C48/80 + IC group — C48/80 was injected at 0 minute and IC at 10 minutes; and 5) IC + C48/80 group — IC was injected at 0 minute and C48/80 at 10 minutes. The studies were carried out by registering and measuring hemodynamic and blood gasometric parameters, including continuous cardiac output.Results1) The effects of the drugs (IC and C48/80) were more evident in the first 20 minutes of recording; 2) hypotensive responses were more pronounced in the C48/80 groups; 3) IC isolated or applied before C48/80 caused transient pulmonary hypertension; and 4) after the first 20 minutes, the pressure responses showed stability with apparent hypotension more pronounced in the C48/80 groups. Clinical observations showed significant hemodynamic instability and catastrophic anaphylactic reactions (agitation, pulmonary hypertension, severe bronchospasm, urticaria, high-intensity cyanosis, violent gastric hypersecretion, and ascites).ConclusionA global results analysis showed differences between groups only in the first 20 minutes of the experiments.

Highlights

  • There are many reasons to believe that the nitric oxide/guanosine 3’5’ – cyclic monophosphate pathway on vasoplegic states is underestimated

  • Arterial hypotension occurred in two groups (C48/80, C48/80 + indigo carmine (IC)); and in group IC + C48/80, the mean arterial pressure (MAP) drop started after the first 10 minutes, when the second injection was performed

  • In 1997, we reported an unprecedented experience with methylene blue (MB) to treat anaphylactic shock from iodine contrast, after high doses of adrenaline and hydrocortisone failed[4]

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Summary

Introduction

There are many reasons to believe that the nitric oxide/guanosine 3’5’ – cyclic monophosphate (or NO/cGMP) pathway on vasoplegic states is underestimated. To study indigo carmine (IC) as an alternative to methylene blue was the investigation rationale. We have noticed in the medical literature the case report of a patient undergoing methylene blue (MB) infusion to check for ureteral perviousness. A more significant and longer-lasting improvement in these parameters with indigo carmine (IC) infusion was observed[1]. We read the first reported case of IC use to treat vasoplegic syndrome in cardiac surgery — in a 78-year-old patient under cardiopulmonary bypass for myocardial revascularization. IC was successfully used after fluid overload, norepinephrine, vasopressin, and MB failed to control arterial hypotension[2]. These two observations suggest that IC may be an alternative agent for reversing vasodilation in conditions such as anaphylaxis and septic shock. IC investigations as a therapeutic option or experimental tool are scarce or inexistent

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