Hypertensive Disorders in Pregnancy Flashcards

1
Q

Definitions;

  1. Pregnancy-induced HTN
  2. Gestational HTN
  3. Pre-eclampsia
  4. Primary/Secondary HTN
A
  1. BP>140/90 after 20w
  2. New HTN after 20w without proteinuria
  3. HTN and proteinuria(>0.3g/24h)
  4. BP>140/90 before pregnancy/before 20w
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2
Q

Classifications:

  1. HTN
  2. Pre-eclampsia
A
  1. a) Mild: 140/90-149/99
    b) Moderate: 150/100-159/109
    c) Severe: 160/110+
  2. a) Mild: Mild/mod HTN+proteinuria
    b) Moderate: Severe HTN+Proteinuria, X maternal complications
    c) Severe: any HTN <34w OR with maternal complications + Proteinuria
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3
Q

PRE-ECLAMPSIA

Epidemiology

A
  • 6% nulliparous

- 15% recurrence rate, up to 50% if severe pre-eclampsia before 28w

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4
Q

Risk f

A
  1. Prev Hx
  2. FHx
  3. Microvasc disease ie diabetes, chronic HTN, CKD, sickle cell disease, autoimmune ie antiphospholipid syndrome
  4. Nulliparity
  5. Twin pregnancy
  6. Obesity
  7. Extremes of age, esp >40y
  8. Long interpregnancy interval
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5
Q

Clinical features:

  1. History
  2. Examination
A
  1. Usually asymptomatic. at late stages: headache, drowsiness, nausea/vomiting, epigastric pain, visual disturbances
  2. HTN first sign usually. Sudden, non-postural oedema, epigastric tenderness, urine dipstick(≥2+)
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6
Q

Maternal Complications

A
  1. Eclampsia(.05% pregnancies)
  2. HELLP
  3. Renal failure
  4. Cerebrovascular haemorrhage
  5. Pulmonary oedema
  6. DIC
  7. Liver failure
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7
Q

Fetal Complications

A
  1. If <34w, Preterm birth(up to 10% preterm deliveries), IUGR
  2. Any gestation, increased risk of placental abruption.
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8
Q

Investigations:

  1. Confirming Dx
  2. Monitoring for maternal complications
  3. Monitoring for fetal complications
A
  1. 2 BP measurements 4h apart. If dipstick positive, urine culture to exclude infection. PCR ≥30mg/nmol. repeat testing as proteinuria can be absent in early disease.
  2. FBC: rapid fall in platelets → HELLP. rise in Hb. LFTs: rise in ALT; bilirubin(haemolysis). Lactate: increases. U&;E’s: rising creatinine, uric acid
  3. USS, Umbilical artery Doppler and if abn, CTG.
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9
Q

Screening

A
  1. High risk(age >40, nulliparity, pregnancy interval>10y, FHx, PMH, BMI ≥ 30, pre-existing vasc disease, pre-existing renal disease, multiple pregnancy) get regular BP and urinalysis, each antenatal visit.
    - HTN w single diastolic measurement of 110/2 measurements of 90,4h apart and/or 1+ preoteinuria require escelation in surveillance.
  2. Uterine artery Doppler at 11-13+6w, BP, biochemical markers to assess risk.
  3. Biochemical markers:
    a) Oxidative response
    - uric acid, urinary kallikrenin, fibronectin

b) 1st trimester
- PAPP-A, inhibin A, Corticotrophin-releasing hormone, activin

c) 2nd trimester
- β-HCG, αFP, unconjugated estriol

*If at risk, Aspirin 75mg from 12w until birth

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10
Q

Management:

Assessment in Day Assessment Unit

A
  1. Mild/moderate HTN + X proteinuria, BP+urinalysis every 2w and USS every 2-4w.
  2. Admit if: proteinuria ≥2+ although no HTN. Discharge if PCR not significant. Definitely admit if symptoms, proteinuria≥2+, Severe HTN, suspected fetal compromise.
  3. if 1+ proteinuria, quantify and review 2d later.
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11
Q

Drugs

A
  1. Antihypertensives:
    - if ≥150/110.
    - Oral nifedipine than IV labetalol. Aim 140/90
    - Benefits: increase mom’s safety, reduce hospitalisation, allow prolongation of pregnancy
  2. Magnesium sulphate:
    - IV loading then IVI
    - usually followed by delivery.
    - Monitor urine output, resp rate, 02 sats, reflexes
  3. Steroids:
    - if gestation <34w
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12
Q

Timing of delivery:

  • ≥1 fetal/maternal complications likely within 2w of proteinuria onset.
    1. Gestational HTN wout fetal compromise.
    2. Mild pre-eclampsia.
    3. Moderate/severe
    4. Severe w complications/fetal distress
A
  1. Monitor, IOL at 40w if Tx req.
  2. by 37w
  3. delivery if 34-36w. <34w, conservative Mx with intensive maternal and fetal surveillance. Clinical deterioration prompts delivery.
  4. DELIVER!!!!!!!
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13
Q

Conduct of delivery

A
  1. <34w, C section
  2. > 34w, IOL w prostaglandins.
  3. Epidural reduces BP
  4. Continuous CTG
  5. BP and fluid balance
  6. Antihypertensives
  7. Avoid maternal pushing at 160/110
  8. Oxytocin over ergometrine at 3rd stage
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14
Q

Postnatal care

A
  1. LFT, platelets, renal fn.
  2. Fluid balance: 80ml/h + losses
  3. CVP if urine output persistently low; frusemide if CVP high, fluids if low. if normal but persistent oliguria, may need dialysis w rising K+.
  4. BP maintained at 140/90. Tx w beta blocker(1st line) OR nifedipine/ACE-i
  5. Long term: GP and community midwives. if persistent proteinuria/HTN at 6w, refer to renal/HTN clinic.
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15
Q

PRE-EXISTING HTN IN PREGNANCY

Epidemiology

A

about 5% pregnancies

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16
Q

Risk f

A

Age, high BMI, FHx, COCP.

Predisposes to HTN needing Tx later in life.

17
Q

Aetiology

A

Primary: Idiopathic. Secondary: Obesity, diabetes, Renal disease. Rare: Phaeochromocytoma, coarctation of aorta, Cushing’s, cardiac disease.

18
Q

Clinical features

A

usually asymptomatic. otherwise, fundal changes, renal bruits, radiofemoral delay.

19
Q

Complications

A

Worsening HTN, pre-eclampsia(6x). perinatal mortality only marginal increase in absence of these.

20
Q

Investigations:

  1. Identifying secondary HTN
  2. Look for coexistent disease
  3. Identify pre-eclampsia
A
  1. Phaeochromocytoma: exclude w two 24h urine collections for VMA
  2. Renal fn. and renal US
  3. Quantify proteinuria at booking and uric acid lvl for comparisons later.
21
Q

Management:

  1. HTN
  2. Risk of pre-eclampsia
A
  1. Stop ACE-i. Labetalol(1st line), Nifedipine(2nd line)

2. Treat as high-risk. More freq antenatal visits. Screen w umbilical artery Doppler. Low-dose aspirin