Diabetes in pregnancy: are we providing the best care ... - HQIP
Diabetes in pregnancy: are we providing the best care ... - HQIP
Diabetes in pregnancy: are we providing the best care ... - HQIP
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was no <strong>in</strong>formation available to panels as to why <strong>the</strong> postmortem exam<strong>in</strong>ation was not carried out despite<br />
be<strong>in</strong>g offered. In one case only external exam<strong>in</strong>ation was performed, and for one case it was documented<br />
<strong>in</strong> <strong>the</strong> medical records that postmortem exam<strong>in</strong>ation was not needed. Overall, 45% (62/137) of babies who<br />
died <strong>we</strong>re documented to have had a postmortem exam<strong>in</strong>ation, which is slightly higher than <strong>the</strong> national<br />
average of 40% <strong>in</strong> 2002-03. 5<br />
Postmortem exam<strong>in</strong>ation fi nd<strong>in</strong>gs <strong>we</strong>re available to <strong>the</strong> panel for 57 out of 62 babies and <strong>are</strong> reported <strong>in</strong><br />
table 5.7. The reported <strong>in</strong>cidence of islet cell hyperplasia and eos<strong>in</strong>ophilic <strong>in</strong>fi ltrates <strong>in</strong> <strong>the</strong> pancreas was<br />
lo<strong>we</strong>r <strong>in</strong> this group of babies than <strong>in</strong> previous reports. 6 It is diffi cult to be certa<strong>in</strong> of <strong>the</strong> reasons for this<br />
difference, but possibilities <strong>in</strong>clude under-report<strong>in</strong>g due to advanced autolysis, a particular problem<br />
<strong>in</strong> <strong>the</strong> pancreas.<br />
Table 5.7<br />
Postmortem exam<strong>in</strong>ation fi nd<strong>in</strong>gs <strong>in</strong> babies who died after 20 <strong>we</strong>eks gestation hav<strong>in</strong>g a postmortem<br />
Specific f<strong>in</strong>d<strong>in</strong>gs reported n (%)<br />
(N=57)* †<br />
Islet cell hyperplasia 6 (11)<br />
Eos<strong>in</strong>ophilic pancreatitis 1 (2)<br />
Cardiomegaly 10 (18)<br />
Vascular thrombosis 0 (0)<br />
No abnormality reported on postmortem 41 (72)<br />
* 5 postmortem exam<strong>in</strong>ation reports <strong>we</strong>re not available.<br />
† There may have been more than one fi nd<strong>in</strong>g reported for any baby undergo<strong>in</strong>g postmortem exam<strong>in</strong>ation.<br />
5.4 Conclusions<br />
Women <strong>in</strong> <strong>the</strong> enquiry <strong>we</strong>re similar to women <strong>in</strong> <strong>the</strong> descriptive study with respect to socio-demographic<br />
characteristics. Due to <strong>the</strong> sampl<strong>in</strong>g methodology for <strong>the</strong> enquiry (see Chapter 4), half of <strong>the</strong> women <strong>in</strong> <strong>the</strong><br />
enquiry had a poor <strong>pregnancy</strong> outcome.<br />
T<strong>we</strong>lve percent of women <strong>in</strong> <strong>the</strong> enquiry had nephropathy and 32% had ret<strong>in</strong>opathy (pre-exist<strong>in</strong>g or<br />
diagnosed for <strong>the</strong> fi rst time <strong>in</strong> <strong>pregnancy</strong>). About half of women <strong>in</strong> <strong>the</strong> enquiry had recurrent hypoglycaemia<br />
dur<strong>in</strong>g <strong>pregnancy</strong> and a fi fth had at least one severe hypoglycaemic episode requir<strong>in</strong>g external help.<br />
Babies with antenatal evidence of fetal growth restriction had a higher proportion of mo<strong>the</strong>rs with<br />
nephropathy comp<strong>are</strong>d to all babies <strong>in</strong> <strong>the</strong> enquiry, and 70% had a poor outcome. Forty one per cent<br />
of babies with antenatal evidence of macrosomia had a poor outcome, which was similar to <strong>the</strong> 50% of<br />
babies <strong>in</strong> <strong>the</strong> whole enquiry sample with a poor outcome.<br />
Sixteen percent of babies who died from 24 <strong>we</strong>eks of gestation up to 28 days after delivery had a cause<br />
of death classifi ed as ‘severe or lethal congenital anomaly’. Women <strong>in</strong> <strong>the</strong> enquiry had a higher proportion<br />
of unexpla<strong>in</strong>ed antepartum fetal death and a lo<strong>we</strong>r proportion of deaths due to immaturity than <strong>the</strong> general<br />
maternity population. Nearly half of all babies who died had a postmortem exam<strong>in</strong>ation.<br />
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