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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 29, No 6, November/December 2018

392

AFRICA

beneficial effect of aspirin is a consequence of an improvement

in the transformation of uterine spiral arteries.

Masotti

et al

.

57

demonstrated a differential inhibition of cyclo-

oxygenase in the prostaglandin synthetic pathway in platelets

and vessels by low doses of aspirin. The finding of aspirin

as a prophylactic measure for placental-mediated disease has

huge implications for first-trimester screening for PE, in that

such screening not only identifies a high-risk group that can

be subjected to close monitoring, but an intervention can be

instituted, with a significant reduction in the disease process. As

noted above, a combination of medical and obstetric history,

maternal characteristics, mean arterial pressure, UA PI, PAPPA

and PLGF could identify a high proportion of pregnancies at risk

for severe PE, IUGR and stillbirths, and use of aspirin in this high-

risk group could substantially reduce adverse perinatal outcomes.

The prophylactic use of low-dose aspirin is associated with a

significant decrease of almost 50% in perinatal death associated

with severe early-onset pre-eclampsia, provided the treatment is

initiated before 16 weeks’ gestation

Conclusion

Central to our understanding of the pathogenesis of early-

onset PE is absolute utero-placental ischaemia, on the basis

of lack of placental vascular transformation between eight

and 16 weeks’ gestation. By contrast, relative utero-placental

ischaemia, due to a mismatch between utero-placental blood

flow and increased demand for nutrients, occurring late in

pregnancy, may be central to the development of late-onset PE.

These pathogenic mechanisms have advanced our understanding

of this condition, leading to better prediction, screening and

intervention modalities.

Screening for PE in the first trimesterwill trigger commencement

of a prophylactic therapeutic intervention with low-dose aspirin,

resulting in a substantial reduction in early-onset PE. Screening in

the second trimester will lead to more focused management of the

screen-positive group, while prediction of adverse foetal outcomes

in established PE in the third trimester, using a combination

of cardiac Doppler, multi-vessel Doppler assessment of foetal

circulation, and biomarkers, could lead to a significant reduction

in foetal perinatal morbidity and mortality rates. Hopefully,

advances in our understanding of this enigmatic disease will lead

to further prophylactic and new therapeutic interventions.

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