Pre-eclampsia
- define as development
of hypertension after 20 weeks of gestationT
- common in smokersF
- asso. with lack of
trophoblastic infiltration of arteries wallsT
- progress to eclampsia
less often when antihypertensive treatmentT
- asso. with increase
risk of abruptioT
Notes:
pre-eclampsia is defines as hypertension of at least
140/90 mmHg recorded on two separate occasions
at least 4 hours apart and in the presence of at least
300 mg protein in a 24-hour collection of urine,
arising de novo after the 20th week of gestation in
a previously normotensive women and resolving
completely by the sixth postpartum week.
Symptoms of pre-eclampsia
• May be asymptomatic
• Headache
• Visual disturbances
• Epigastric and right upper abdominal pain
Signs of pre-eclampsia
• Elevation of blood pressure
• Fluid retention (non-dependent oedema)
• Brisk reflexes
• Ankle clonus (more than three beats)
• Uterus and fetus may feel small for gestational age
Risk factors for pre-eclampsia
Predisposing factors for the development of pre-eclampsia
include:
• conditions in which the placenta in enlarged (multiple
gestation, diabetes, hydrops)
• pre-existing hypertension or renal disease
• pre-existing vascular disease (such as in diabetes or
autoimmune vasculitis)
Organ-specific changes associated with
pre-eclampsia
Cardiovascular
• Generalized vasospasm
• Increased peripheral resistance
• Reduced central venous/pulmonary wedge pressures
Haematological
• Platelet activation and depletion
• Coagulopathy
• Decreased plasma volume
• I ncreased blood viscosity
Renal
• Proteinuria
• Decreased glomerular filtration rate
• Decreased urate excretion
Hepatic
• Periportal necrosis
• Subcapsular haematoma
Central nervous system
• Cerebral oedema
• Cerebral haemorrhages
Investigations for pre-eclampsia
These investigations will be repeated at intervals
depending on the overall clinical picture.
• Urinalysis by dipstick (quantitatively inaccurate).
• 24-hour urine collection (total protein and creatinine
clearance) .
• Full blood count (platelets and haematocrit) .
Blood chemistry (renal function, protein
concentration).
• Plasma urate concentration.
• Liver function.
• Coagulation profile.
Ultrasound assessment:
- fetal size
- amniotic fluid volume
- maternal and fetal
- Dopplers.
Management and treatment
The mainstay of treatment for pre-eclampsia remains
ending the pregnancy by delivering the fetus (and the
placenta).
The principles of management of pre-eclampsia are:
• early recognition of the symptomless syndrome,
• awareness of the serious nature of the condition in
its severest form,.
• adherence to agreed guidelines for admission to
hospital, investigation and the use of
antihypertensive and anticonvulsant therapy,
• well-timed delivery to pre-empt serious maternal
or fetal complications,
• postnatal follow-up and counselling for future
pregnancies.
The aim of antihypertensive therapy is to lower the
blood pressure and reduce the risk of maternal cerebrovascular
accident without reducing uterine blood
flow and compromising the fetus.
drugs
Labetolol is an
alpha-blocking
and beta-blocking
agent.
It can be
given orally or intravenously
and has
a good safety record in pregnancy.
Methyldopa is a
centrally acting antihypertensive agent.
It, too, has
a long-established safety record in pregnancy,
but can only be
given orally and takes upwards
of 24 hours
to take effect.
Nifedipine is a
calciumchannel
blocker with
a rapid onset of action.
It can,
however, cause
severe headache that may mimic worsening
disease.
In severe
cases of fulminating disease, an intravenous
infusion of hydralazine or labetolol can be titrated
rapidly against
changes in the blood pressure.
The drug of
choice for the treatment of eclampsia is
magnesium
sulphate. This is
given intravenously and has
been shown
to reduce the incidence of further convulsions
in women with eclampsia.
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