Newborns with a Family History of MCADD Medium-Chain Acyl-CoA Dehydrogenase Deficiency JCG0323v2

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Overview

The joint Trust Guideline for Babies with MCADD are at risk of encephalopathy and death in the first few days of life. Recognition of the risk in a baby with a family history of MCADD followed by simple measures to ensure an adequate supply of milk or alternative sources of glucose can prevent morbidity and mortality.

Categories
Clinical
Reference
Date Uploaded
27.05.2016
Date Review
23.05.2019
File Size
107Kb


Clinical Guidelines
This guideline has been approved by the Trust's Clinical Guidelines Assessment Panel as an aid to the diagnosis and management of relevant patients and clinical circumstances. Not every patient or situation fits neatly into a standard guideline scenario and the guideline must be interpreted and applied in practice in the light of prevailing clinical circumstances, the diagnostic and treatment options available and the professional judgement, knowledge and expertise of relevant clinicians. It is advised that the rationale for any departure from relevant guidance should be documented in the patient's case notes.
The Trust's guidelines are made publicly available as part of the collective endeavour to continuously improve the quality of healthcare through sharing medical experience and knowledge. The Trust accepts no responsibility for any misunderstanding or misapplication of this document.