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      Methaemoglobinaemia with G6PD deficiency: rare cause of persistently low saturations in neonates.

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          Abstract

          We report a very rare case of methaemoglobinaemia associated with glucose 6 phosphate dehydrogenase (G6PD) deficiency, complicating a respiratory illness in a preterm neonate. This neonate had consistently low saturation readings despite being ventilated at moderately high pressures in 100% oxygen. An arterial blood gas confirmed a high methaemoglobin level and a high pO2, inconsistent with the saturations. In addition, the bilirubin increased to exchange levels and was difficult to control with quadruple phototherapy. A double volume exchange transfusion was performed, which reduced both bilirubin and methaemoglobin. The pulse oximetry then started to correlate well with pO2. G6PD deficiency was confirmed.

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          Author and article information

          Journal
          Acta Paediatr
          Acta paediatrica (Oslo, Norway : 1992)
          Wiley
          1651-2227
          0803-5253
          Jul 2011
          : 100
          : 7
          Affiliations
          [1 ] Department of Paediatrics, Sandwell & West Birmingham NHS Hospitals Trust, Birmingham, UK.
          Article
          10.1111/j.1651-2227.2011.02278.x
          21418105
          20e1b048-79ad-43b6-8ccd-2cd8ad931373
          History

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