hypertensive disease pregnancy Flashcards

1
Q

causes of preexisting hypertension in a young person (if dx in first trimester)
+ what signs / inx can help?

A

Renal - renal artery stenosis (lsiten for bruit, renal USS) urinalysis Hb /protein, casts, Cr
CKD from GN, polycystic kidney disease
Cardiac - aortic coarctation (look for radiofemoral delay)
Endocrine - hyperparathyroidism (calcium), cushings, conns syndrome, phaeochromocytoma (urinary catecholamines) Low K (hyperaldosteronism / conns)

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2
Q

What are the risks of essential HTN in pregnancy (%)

A

25% risk of PET
28% PTB
17% IUGR
4% Abruption and death

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3
Q

GHTN

Rate of development to PET

A

GHTN only 15% develop PET (less the later the onset is)

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4
Q

Severe Complications of PET

A
Eclampsia - tonic clonic grand mal seizure (only 1/3 have HTN dx in the week before they have an eclamptic seizure - antepartum 45%, intrapartum 18% PN 36%) 
Stroke
Cortical blindness - from posterior reversible encephalopathy syndrome - oedema to the CNS 
Respiratory distress / pulmonary oedema
HELLP
DIC
Renal failure
Hepatic rupture
Transient L  venticular dysfunction
placental - abruption, death, IUGR
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5
Q

PET risk factors

A
Medical
Renal disease, 
Preexisting HTN OR 3.5 
Antiphospholipid syndrome RR 9 
Connective tissue disease
Sickle cell
Diabetes (preexisting or GDM) RR 3.5 
Obstetric 
Primip (2-3X increase)
twins (2X)
Prev PET (7X) 
Long interpreg interval (over 10 years) (2-3X) 
Hydrops / large placenta
Molar pregnancy / triploidy 

General
over 40
obese
FHX - mother had it - 25% chance, sister 40%

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6
Q

MAP How do you calculate

A

Mean arterial pressure

D + 1/3 (S-D)

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7
Q

nifedipine
Mode of action
Side effects

A

Calcium channel blocker

Side affects include flushing, headache, oedema

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8
Q

labetalol
Mode of action
contraindications
Side effects

A

a and b adrenergic blocker
BD - QID
contraindicated in asthma

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9
Q

ACEi and Angiotensin II receptors

What affects on the fetus in pregnancy

A

Teratogenic
T1 - cardiovascular and neurological malformations
T2/3 oligohydramnios, renal failure, hypotension, decrease skull ossification, hypocalvaria renal tubular dysgenesis, IUD

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10
Q

Magnesium sulphate dosing
Indications for Mg levels
Signs of overdose

A

Loading dose 4g diluted in saline over 15-20mins then 1-2g / hour maintenance for 24-48 hours
If seizes again 2-4g IV over 10 mins (recurrence on MgSO4 10%)
IM ok too
If AKI then half maintenance dose
Indications for MgSO4 levels are AKI, liver impairment or oliguric

Side effects - loss deep tendon reflex as neuromuscular blockade, Double vision, slurred speech, respiratory depression and cardiac arrest

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11
Q

Indications for aspirin prophylaxis

Aspirin reduces the risk of PET by 15% but the NNT is 90

A

From 12 weeks

one major
Prev PET
T1 or T2 diabetes
Chronic HTN
Chronic kidney disease
Autoimmune disease (SLE, antiphospholipid syndrome) 
OR
more then one moderate risk factor
First pregnancy
40 or older
Preg interval over 10 years
BMI 35+ at first visit
Fhx PET
Multiple pregnancy
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12
Q

BP treatment thresholds
SOMANZ
Why treat high BPS

A

Antihypertensives for 160/110
Stat treatment for 170/110

cerebral haemorrhage, posterior reversible encephalopathy syndrome, hypertensive encephalopathy

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13
Q

How to check BP

  • position
  • sounds
A

Sitting, feet flat on floor, arm at the level of the heart
Supine should be avoided
in labour - BP maybe measured in lateral recumbency

Correct cuff size - the bladder must cover over 80% of the arm circumference

Sounds
K1 - first sound heard
K4 (muffling - best not to use this)
K5 - Disappearance of the sound completely

rate of deflation <2mm per second

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14
Q

How do you diagnose PET when preexisting Proteinurea or HTN

A

You cannot use worsening BP or PCR as an indication of PET
You also cannot use SGA as this is independent of PET
You need maternal systemic effects or fetal effects eg oligo, abn dopplers

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15
Q

CLASP study

outcomes

A

In our multicentre study 9364 women were randomly assigned 60 mg aspirin daily or matching placebo.

Overall, the use of aspirin was associated with a reduction of only 12% in the incidence of proteinuric pre-eclampsia, which was not significant. Nor was there any significant effect on the incidence of IUGR or of stillbirth and neonatal death. Aspirin did, however, significantly reduce the likelihood of preterm delivery (19.7% aspirin vs 22.2% control; absolute reduction of 2.5 [SD 0.9] per 100 women treated; 2p = 0.003). There was a significant trend (p = 0.004) towards progressively greater reductions in proteinuric pre-eclampsia the more preterm the delivery.

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16
Q

CLASP study

inclusion

A

74% were entered for prophylaxis of pre-eclampsia, 12% for prophylaxis of IUGR, 12% for treatment of pre-eclampsia, and 3% for treatment of IUGR.

17
Q

CLASP - is there harm to aspirin?

A

Aspirin was not associated with a significant increase in placental haemorrhages or in bleeding during preparation for epidural anaesthesia, but there was a slight increase in use of blood transfusion after delivery.

18
Q

CLASP findings

A

Findings do not support routine prophylactic or therapeutic administration of antiplatelet therapy in pregnancy to all women at increased risk of pre-eclampsia or IUGR.

Non significant reduction in PET
Aspirin did, however, significantly reduce the likelihood of preterm delivery (19.7% aspirin vs 22.2% control; absolute reduction of 2.5 [SD 0.9] per 100 women treated; 2p = 0.003). There was a significant trend (p = 0.004) towards progressively greater reductions in proteinuric pre-eclampsia the more preterm the delivery.

Low-dose aspirin may be justified in women judged to be especially liable to early-onset pre-eclampsia severe enough to need very preterm delivery. In such women it seems appropriate to start low-dose aspirin prophylactically early in the second trimester.

19
Q

How does aspirin help the placenta?

A

Aspirin works by irreversibly inhibiting almost all the platelet cyclo oxygenase activity thereby blocking synthesis of the thromboxane - a vasoconstrictor and platelet aggregating agent

20
Q

Pre pregnancy counselling previous PET

A

15% risk recurrence (7X increased)
This number is increased if any baseline medical conditions - CKD, HTN, APLS
Higher recurrence if HELLP or early onset PET
Consideration of lifetime cardiovascular disease risk - candidates for screening and possible intervention
PET increases lifetime risk of HTN (3-4X) IHD (2X) and CVS

21
Q

Indications for aspirin for PET prophylaxis

A

Major - 1 of these
Major risk factors for pre-eclampsia include:
 Previous pre-eclampsia requiring delivery before 37weeks
or
With haemolysis, elevated liver enzymes, and/or low platelets
(HELLP Syndrome)
 Predisposing medical conditions
• Autoimmune e.g.
o Systemic Lupus Erythematosus
o Scleroderma
o Anti-phospholipid syndrome
• Chronic hypertension
• Diabetes type 1 and 2
• Any chronic kidney disease
 Assisted conception with oocyte donation
 Family history of pre-eclampsia (mother and/or sister)

Minor - more then 1

22
Q

When to take aspirin

A

At night
best at 12 weeks
evidence best before 16 weeks
can give up to 20 weeks

23
Q

What are the benefits of calcium

Who gets it ?

A

The Cochrane review demonstrated that calcium supplementation also reduces the overall
risk of pre-eclampsia, [RR 0.45 (95% CI 0.31 to 0.65); I² = 70%]. As above the effect was
greatest for women with low calcium diets and women at high risk of pre-eclampsia.
Importantly calcium supplementation also reduced the risk of preterm birth [RR 0.76 (95% CI
0.60 to 0.97); I² = 60%], maternal death or serious maternal morbidity [RR 0.80 (95% CI 0.65
to 0.97); I² = 0%].
Calcium did not reduce the rate of SGA infants and should not be
prescribed for prevention of SGA alone.

24
Q

Aspirin contraindications ?

A

Contraindications to LDA (rare in women of reproductive age)
• Previous peptic ulcer
• Asthma induced by Non-Steroidal Anti Inflammatory Drugs
• Allergy to aspirin

25
Q

NNT for aspirin and calcium to prevent PET

A

NNT for calcium 7

NNT for aspirin 56

26
Q

what is the harm of high levels of Vit C and E

A

LBW babies

27
Q

What BPS need Tx

What BP needs urgent treatment

What are Tx targets

A

> 160/110

Who needs tx
BPs >140/90

BP targets are 130-150/80-100

28
Q

Options for tx severe hypertension
160/110
What are their onsets

A

nifedipine 10 mg oral conventional release
onset of action 30-45 minutes - max effect in 30 minutes
repeat tab after 30-45 minutes
max 80 mg daily

Labatelol
20 mg IV bolus over 2 minutes
onset: 5 minutes
Max effect 10-15 minutes

Repeat every 10 minutes with 40-80mg
Max 300 mg

Hydralazine
5-10 mg IV bolus over 3-10 minutes 
(5 mg if fetal compromise)
onset 20 minutes
max effect 10-18 minutes
repeat q 20 mins 
max 30 mg 
consider crystalloid bolus 200 mg
29
Q

MgSO4 antidote ?

A

IV calcium gluconate

30
Q

Signs of MgSO4 toxicity

A

– reflexes are absent
– the respiratory rate is less than 12 per minute, or
– the urine output drops below 100 mL in 4 hours.