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Saving Mothers' Lives: - Public Health Agency for Northern Ireland

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Obesity was present in 55% of these cases and morbid obesity was present a quarter of women who<br />

died of ischaemic heart disease/myocardial infarction. A similar picture was seen <strong>for</strong> deaths from sudden<br />

adult death syndrome (SADS). Abdominal obesity is the <strong>for</strong>m of obesity most strongly associated with<br />

the metabolic syndrome with its associated increased risk of cardiovascular disease. Clinically there<br />

is increased waist circumference with raised triglycerides, total cholesterol and low concentrations of<br />

high-density lipoprotein cholesterol in the peripheral blood. Non-esterifi ed fatty acids are also frequently<br />

raised. Raised levels of non-esterifi ed fatty acids have also been associated with sudden death from<br />

cardiovascular disease 13 . Measurement of non-esterifi ed fatty acids at postmortem is unreliable but a<br />

good proxy is measurement of abdominal circumference particularly in ratio to the hip circumference 14 . For<br />

women an abdominal girth greater than 88 centimetres would be a criterion helping to defi ne the metabolic<br />

syndrome 15 .<br />

Ischaemic and unascertained<br />

Three of the 12 women who died from ischaemic heart disease and whose cases were assessed had no<br />

postmortem. Three autopsies were poor but the other six were good or better. All these women had clinical<br />

risk factors such as smoking, obesity or diabetes. The clinical history was often suggestive in the cases<br />

of women who died from sudden adult death syndrome (SADS). One woman, who had been investigated<br />

some years earlier <strong>for</strong> episodes of collapse that had been attributed to vasovagal faints, collapsed and<br />

died whilst talking to someone. Two other cases may have been due to SADS but cannot be adequately<br />

categorised; the coroner failed to release the autopsy report in one case whilst in the other the autopsy<br />

was so bad that an attributable cause may have been missed. Of the other cases of SADS where autopsy<br />

reports were available, one was adequate and another poor but the majority were very good and had<br />

clearly excluded other potential causes. For example:<br />

A young girl was found dead a few months after delivery and a thorough, detailed, autopsy failed<br />

to demonstrate a cause of death. Cardiomyopathy was suspected but excluded after referral to a<br />

cardiac pathologist and so a diagnosis of SADS was made. Subsequently cardiac tissue that had<br />

been submitted <strong>for</strong> genetic studies showed a mutation which was not in the European Society of<br />

Cardiology database.<br />

The pathogenicity in this particular case is not known and can obviously only be determined when more<br />

cases are identifi ed. This would require more detailed investigation of cardiomyopathies and SADS. It<br />

is, however, vital that there is further screening of the family members when a young woman under the<br />

age of 40 years has an unascertainable cause of death. In one study there were cardiac abnormalities<br />

in 40% of the families associated with such deaths. The causes included electrical conduction problems,<br />

cardiomyopathies of all types and hypercholesterolaemia 16 .<br />

Arterial dissections<br />

There were 17 deaths from arterial dissection subject to pathological review. Of these eight were in the<br />

aorta, four in the splenic artery, three in the coronary arteries and one each in the external iliac and the<br />

basilar arteries.<br />

All of the postmortems on the aortic dissections were per<strong>for</strong>med to a high standard. Two women were<br />

morbidly obese, two had Marfanoid features, the father of another had died of aortic dissection and one<br />

had three separate aortic dissections with only the third rupturing. One further woman died of pulmonary<br />

embolus: the dissection had re-entered to create a double barreled aorta. In all but one case histology<br />

revealed features such as organisation of the blood within the aortic wall indicating that the dissection<br />

had started some days prior to fi nal rupture though the duration of the clinical symptoms had rarely been<br />

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