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Hypoglycaemia in Clinical Diabetes

Hypoglycaemia in Clinical Diabetes

Hypoglycaemia in Clinical Diabetes

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CONSEQUENCES OF HYPOGLYCAEMIA 205of mild ventricular atrophy <strong>in</strong> those with early onset diabetes. None of the f<strong>in</strong>d<strong>in</strong>gs wererelated to the presence of microvascular disease or diabetes duration, suggest<strong>in</strong>g that thecumulative effects of hyperglycaemia were unlikely to be causative. However, no def<strong>in</strong>ite l<strong>in</strong>kwas confirmed between exposure to severe hypoglycaemia and any of these defects, althoughthe study was limited by retrospective report<strong>in</strong>g of the history of preced<strong>in</strong>g hypoglycaemiaover a long period of time (Ferguson et al., 2005). Another study did not f<strong>in</strong>d a difference<strong>in</strong> tests of cognitive function over a period of 18 months <strong>in</strong> 142 patients tak<strong>in</strong>g part <strong>in</strong> astudy exam<strong>in</strong><strong>in</strong>g the impact of <strong>in</strong>tensive therapy versus usual care (Wysocki et al., 2003).The study group had a wide age range from 6–15 years and data from younger childrenwere not analysed separately.Although there are methodological problems <strong>in</strong> design<strong>in</strong>g studies to assess long-termcognitive function <strong>in</strong> children who have an ongo<strong>in</strong>g chronic disorder, these studies do raiseanxieties. It is felt that until hypoglycaemia can be reliably avoided, glycaemic control shouldbe less <strong>in</strong>tensively managed <strong>in</strong> younger children to avoid the risk of severe hypoglycaemia.This would put younger children at greater risk of develop<strong>in</strong>g the long-term microvascularcomplications of diabetes <strong>in</strong> an attempt to avoid the possible cognitive defects that may beassociated with recurrent hypoglycaemia.Hypoglycaemic HemiplegiaThis is a rare complication of acute hypoglycaemia <strong>in</strong> which the patient recovers fromthe hypoglycaemia with a transient hemiparesis last<strong>in</strong>g no more than 24 hours. Whenneuroimag<strong>in</strong>g is performed it is rare to f<strong>in</strong>d an abnormality. There is no evidence of anysevere sequelae to this neurological manifestation of severe neuroglycopenia (Pocecco andRonfani, 1998).Fear of <strong>Hypoglycaemia</strong>Both the children with diabetes and their parents worry about the prospect of a severe episodeof hypoglycaemia (Gold et al., 1997; Clarke et al., 1998; Gonder-Frederick et al., 1997;Marrero et al., 1997; Nordfelt and Ludvigson, 2005) (see Chapter 14). In one study severehypoglycaemia caused more fear than the prospect of an episode of diabetic ketoacidosis(Nordfelt and Ludvigson, 2005). Although there is little evidence that this modifies behaviourto attempt hypoglycaemia avoidance, such as relax<strong>in</strong>g glycaemic control or eat<strong>in</strong>g moresnacks, the adverse effects on quality of life should not be underestimated (Gold et al.,1997).Prediction of Nocturnal <strong>Hypoglycaemia</strong>Overnight glucose profiles have been shown to be extremely variable. As a result studies ofovernight hypoglycaemia have been unable to provide a ‘safe’ glucose value with which togo to bed. What is more useful is the fast<strong>in</strong>g blood glucose concentration on the follow<strong>in</strong>gmorn<strong>in</strong>g. One study showed that the median fast<strong>in</strong>g blood glucose at 07:00 hours wassignificantly lower follow<strong>in</strong>g hypoglycaemia than a night with no hypoglycaemia (3.7[1.4–10.6] versus 8.5 [3.8–19.2] mmol/l, p = 000001) (Matyka et al., 1999a) (Figure 9.2).

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