Introduction
◦ Complicates upto 10% of pregnancies
◦ Represents significant Maternal and Perinatal morbidity and Mortality
◦ Hypertensive disorders of pregnancy is an umbrella term encompassing
preexisting , gestational hypertension ,preeclampsia and it complications
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Classification and definitionof hypertension in
pregnancy
A. Gestational hypertension
B. Pre-eclampsia
C. Chronic hypertension
D. Chronic hypertension with superimposed pre-eclampsia
E. White coat Hypertension
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6.
A. Gestational hypertension
Hypertensionafter 20 weeks gestation on two or more
occasions 4 hours apart without proteinuria on a previously
normotensive patient and resolves within 6 weeks post
delivery
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7.
B. Chronic hypertension
Essential:
Bloodpressure greater than 140/90 mmHg preconception or prior to 20
weeks without an underlying cause
Secondary Hypertension :
chronic kidney disease
endocrine disorders
coarctation of the aorta
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C. Chronic hypertensionwith superimposed
pre-eclampsia
The new development after 20 weeks gestation of one or
more of the features of pre-eclampsia in a patient with
preexisting chronic hypertension
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D. Pre-eclampsia
New onsetHypertension that arises after 20 weeks of gestation and returning
to normal within 6 weeks post partum ,and is associated with proteinuria.
Further classified
1. Pre eclampsia with Severe Features
2. Imminent Eclampsia
3. Eclampsia
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10.
Risk factors ofHypertension In
Pregnancy
◦ Maternal
◦ Primigravida
◦ Family history of pregnancy induced hypertension
◦ DM, Chronic HPT, Renal insufficiency
◦ Anti-phospholipid syndrome and inherited thrombophilia
◦ Extremes of maternal age (18< or >35)
◦ Vascular or connective tissue disease
◦ High BMI
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Fetal
◦ Multiple gestation
◦Unexplained fetal growth restriction
◦ Previous unexplained stillbirths
◦ Hydrops fetalis
Paternal
Primi paternity
Male Partner whose previous partner had preeclampsia
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Socio economic
◦ Lowsocio economic status
◦ Recreational drug use
◦ Smoking
◦ Alcohol
◦ Stress
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PRE-ECLAMPSIA
PATHOPHYSIOLOGY
• Immune factors, genetic factors , dietary factors, CKD , unknown
factors
• Trophoblastic maladaptation
• Reduced uteroplacental perfusion
• Cellular anoxia
• Release of angiogenic factors, apoptotic cells and trophoblastic debris
• Vascular endothelial damage
• Organ system involvement
• Clinical signs and then ^BP, proteinuria and IUGR
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Chronic
hypertensio
n
Pre-
eclampsia
Superimposed pre-
eclampsia
age Usually> 30
years
Young or > 35
years
Usually >30 years
gravidity multigravida primigravida multigravida
Order of signs Fall pregnant
while
hypertensive
Weight gain
HPT
Oedema
proteinuria
Already hypertensive.
Develops severe HPT and
proteinuria
Eclampsia
Risk:maternal and fetal Low to mild Mild to high high
Risk of recurring in
subsequent pregnancies
high Small high
Renal function Relatively
unaffected
Early increase
in
urea,creatinine
,urates
Incr urea and creatinine but
urate can rise
disproportioally d/t pre-
eclmpsia
DIFFERENCES BETWEEN THESE DISORDERS
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Principles in managementof pre-
eclampsia
Admit to hospital :
Establish aetiology of hypertension
• To plan treatment
• To evaluate prognosis
History-taking:
• Previous history of hypertension
• Family History of Hypertension
Evidence of other organ involvement
• Cardiac
• Renal
Continuing Assessment
• 4-hourly BP recording
• Maternal investigations
• Foetal surveillance
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Principles in managementof pre-
eclampsia
Control BP
prevent eclampsia
Check and correct complications
Assess fetal compartment
Definite management is delivery
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Investigations
Urine dipstick:
1+ iseqv. to ± 300mg proteinuria
2+ is eqv. to ± 1000mg protein=> nephrotic range
proteinuria
3+ is eqv. to ± 4000mg/dl
FBC: ↓platelets, Hb
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Management of pre-eclampsia
Managementis done according to clinical group:
Patients before with Severe early onset PET 24 weeks gestation: TOP is advised
Between 24 and 34 weeks: Room for conservative management if both Maternal and
Fetal Compartments are stable
After 34 weeks: Delivery
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Prevention of Pre-eclampsia
◦LOW DOSE ASPIRIN (1mg/kg/daily)
◦ Indications include:
◦ History of early-onset pre-eclampsia
◦ Collagen Vascular Disease
◦ Recurrent pre-eclampsia in previous pregnancies
◦ Previous hypertension with perinatal mortality
◦ Recurrent foetal growth impairment of unknown aetiology
◦ Calcium (100-1500g/daily) is also used in the prevention of pre –eclampsia.
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Management of Pre-
eclampsia
◦AIM of management is to maximise good perinatal outcomes without
endangering maternal health.
◦ ANTIHYPERTENSIVE TREATMENT.
◦ ASSESSING FOR COMPLICATIONS
◦ FETAL MONITORING
◦ USE OF MAGNESIUM SULPHATE
◦ TIMING AND MODE OF DELIVERY
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CONTROL OF BLOODPRESSURE
DRUGS SUITABLE IN PREGNANCY
◦ Alpha-receptor antagonists: Methyldopa
Loading dose: 1-2 g po
Continuation: 500mg 3 times daily to maximum of 2g daily
◦ Alpha and beta-receptor antagonists: Labetalol
Can be used as a short acting agent
◦ Calcium channel blockers: Nifedipine
Long acting used both ante and post partum
Or short acting agent: 10 mg oral
◦ Arteriolar Vasodilators: Hydralazine
Adjunct to methyldopa
Can be used as a rapid agent
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Cont…
◦ If BPis >140/90, commence treatment with Aldomet (Methyldopa) at
a dose of 500mg 6 hourly or 8 hourly depending on BP. Should the
BP be poorly controlled on Aldomet ie. 2 BP spikes in 24 hours
requiring use of a rapid-acting agent, add a second agent.
◦ Adalat (Nifedipine) starting at 10mg 8 hourly up to a maximum of
20mg 6-hourly
◦ Hydralazine is the third-line agent and can be started at a dose of 1mg
8 hourly up to a maximum of 7mg 8 hourly.
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Cont.….
◦ BP >170/110 - should be treated as a hypertensive emergency
◦ Start a Labetalol infusion: 200mg in 200mls normal saline at 20/40/80 ml.hr
titrated against the BP every 30 minutes. Caution in patients with tachycardia.
◦ Alternatively administer Nifedipine capsules 10 mg orally immediately, and if
necessary 20-30 minutes later. Avoid sublingual Nifedipine.
◦ The goal should be to lower BP to 140/90 – 150/90.
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Cont..
◦ Goal: Maintenanceof maternal well-being and
delivery of infant who will survive and develop
normally.
◦ Thus, delivery is delayed
◦ Unless deterioration in the maternal or foetal condition
becomes a dominant feature.
◦ Betamethasone 12mg 12-hourly (two doses) to stimulate
foetal maturity for pregnancies less than 34 weeks
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ECLAMPSIA-MANAGEMENT
◦ Check circulation,airways and breathing
◦ Place the patient in the left lateral position
◦ Administer oxygen – 6 to 8L / per minute
◦ Give Magnesium Sulphate for treatment and prevention of further
seizures
◦ Reduce blood pressure as per regimen
◦ Investigate for complications
◦ Definitive management is delivery
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MAGNESIUM SULFATE
◦ MgSO4used to control convulsions and prevent further convulsions.
◦ SIBAI’S INTRAVENOUS REGIMEN
Loading dose: 6g in 200ml over 20mins IV
Maintenance: 2g/hour IV
Continued until 24 hours post-delivery.
◦ PRITCHARD’S INTRAMUSCULAR REGIMEN
Loading dose:14g (4g IV over 5 mins and 10g IM, 5g in each buttock)
Maintenance: 5g 4-hourly IM.
This is used in primary care .
◦ ZUSPAN REGIMEN
Loading dose: 4g in 200ml IV over 15-20 minutes
Maintenance : 1 g hourly given by infusion pump 32
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Monitoring
◦ Check thefollowing signs every 4 hours before commencing the
next dose of magnesium sulphate.
◦ Presence of peripheral knee or arm reflexes
◦ Respiratory rate above 16 per minute
◦ Urine output of more than 30 mls per hour
◦ Monitor
◦ Blood pressure recording every 10-20 minutes.
◦ ½ Hourly pulse and urine output.
◦ Pulse oximeter if available