Methaemoglobinaemia: From pathophysiology to contemporary clinical management.

Methaemoglobin (MetHb) is an oxidised form of haemoglobin that cannot carry oxygen, caused by genetic mutations, enzyme deficiencies, or exposure to oxidising agents like dapsone and cocaine-derived anaesthetics. Symptoms emerge at MetHb concentrations above 10% and include cyanosis, confusion, arrhythmias, and potentially death, though arterial blood gas readings appear misleadingly normal. Intravenous methylene blue is the first-line treatment for symptomatic cases, with alternative therapies including high-dose vitamin C and exchange transfusion, though evidence for optimal use of alternatives remains limited.

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IV methylene blue is first-line for symptomatic methaemoglobinaemia; recognising misleadingly normal ABGs is key to timely intervention.

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