Wk 3: Hypertension/Pre-eclampsia/Clinical Deterioration Flashcards

1
Q

What blood pressure is defined as pregnancy hypertension and thus the threshold for pre-eclampsia screening?

A

Systolic blood pressure (BP)= ≥ 140mmHg
and/or
Diastolic blood pressure= ≥90 mmHg
*some require proteinuria

These measurements should be confirmed by repeated readings over several hours.
- clinicians should commence therapy to target a blood pressure less than or equal to 140/90

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2
Q

What are the thresholds hypertension?

A

Mild Hypertension
Systolic BP 140 - 149
Diastolic BP 90 - 99

Moderate Hypertension
Systolic BP 150 -159 mmHg
Diastolic BP - 100-109 mmHg

Severe Hypertension
Systolic BP ≥160 mmHg (some say 170)
and/or
Diastolic BP ≥110 mmHg

Severe Hypertension requiring immediate treatment
Systolic BP ≥170 mmHg
and/or
Diastolic BP ≥ 110 mmHg

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3
Q

Define gestation/pregnancy-induced hypertension

A
  • New onset of hypertension after 20 weeks gestation
  • without any maternal or fetal features of pre-eclampsia
  • BP returns to normal within 3 months postnatally
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4
Q

What is a key practice point for managing sever pre-eclampsia?

A

Lower blood pressure carefully, as inadequate placental perfusion may occur where placental circulation has adapted to a higher blood pressure.

If lowered to quickly, can cause;
- cerebral haemorrhage
- hypertensive encephalopathy

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5
Q

What is the management of severe hypertension?

A
  • Admit to Hospital for Acute Treatment
  • Do not allow BP to fall below 140/80
    Antihypertensive therapy with (for all those with systolic >170 or diastolic >110);
  • Nifedipine, maximum 40 mg, oral
  • Labetalol, 20–80 mg, IV bolus over 2 minutes
  • Hydralazine, 5–10 mg, IV bolus over 5 minutes administered by a medical officer, or IM injection

Fluid restriction
- Nil by mouth
- 80 ml/hr IV crystalloid

Observations during acute Treatment of severe hypertension
- 15 minutely BP
- 30 minutely - complete set of vital signs, and assessment of response to treatment
- continuous oxygen saturation monitoring
- continuous fetal monitoring.

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6
Q

What assessment should be considered for hypertension?

A

Maternal assessment
- history: headache, visual disturbances, epigastric or right upper quadrant pain
- Vital signs: BP, pulse, respiratory rate, temperature
- General examination: abdominal palpation, reflexes, clonus.
- Spot urine PCR
- FBE
- platelets are < 100 x 109/L include:
- Liver function test - AST, ALT and LDH
- Clotting profile - coagulation profile (APTT, PT, fibrinogen)
- group and hold
- Urea, creatinine, electrolytes
- Abdominal palpation
- Reflexes and clonus
- Oedema
- MSU
- uric acid (in some organisations)

Fetal assessment
- Fetal movements
- CTG if >28wks
- US assessment of fetal growth,
AFI, UA dopplers
- Antenatal corticosteroids (Betamethasone) administration to a woman who is expected to birth pre-term should be considered
- Antenatal Magnesium Sulphate administration to the woman who is expected to birth pre-term (<30 weeks gestation) is recommended for the purpose of fetal neuroprotection

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7
Q

What further investigations should be considered for suspected pre-eclampsia?

A

Features of pre-eclampsia:
- urinalysis for protein
- urine microscopy

Thrombocytopenia or a falling
haemoglobin:

  • investigate for disseminated
    intravascular coagulation
    and/or haemolysis
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8
Q

What is the management for moderate hypertension?

A

Ongoing treatment with antihypertensive medication
= Aim for BP <150/100

First line agents:
- Labetalol 100–400 mg TDS
- Methyldopa 250–750 mg TDS

Second line;
- nifedipine

Antenatal care – aim for BP <150/100
- Individualise schedule of antenatal visits
- BP monitoring as clinically indicated
- Routine CTG not indicated
- 28–30 weeks US for growth
- 30–32 weeks US for growth

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9
Q

What is the management of mild hypertension?

A
  • optional antihypertensive therapy
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10
Q

What are some fetal and maternal indications for immediate delivery in the context of hypertension?

A

Maternal
- Inability to control hypertension
- uncontrollable pre-eclampsia
- uncontrolled hypertension
- Deteriorating biochemistry
aka deteriorating platelet count, deteriorating liver function and deteriorating renal function.
- Placental abruption
- Persistent neurological symptoms
- Persistent epigastric pain, nausea or vomiting with abnormal LFTs
- Acute pulmonary oedema
- Gestational age > 37 weeks
- HELLP Syndrome

Fetal
- Severe fetal growth restriction
- Abnormal CTG requiring immediate delivery
- gestational age >37wks

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11
Q

Explain the drug methyldopa. Including the;
- dose
- actions
- contraindications
- practice points

A

Dose: 250 mg-750 mg
every 8 hours/TDS

Actions: centrally acting adreergic agonist

Contraindications: depression

Practice points:
- Slow onset of action over
24 hours
- dry mouth
- sedation
- depression
- blurred vision

Withdrawal effect:
rebound hypertension

Prescribed;
- hypertension of any kind in pregnancy e.g. chronic hypertension

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12
Q

Explain the drug labetalol for ongoing treatment and acute treatment of hypertension. Including the;
- dose
- actions
- contraindications
- practice points

A

Dose:
Ongoing: 100mg-400mg every 8hrs/TDS
Acute: 20–80 mg; max 80mg/dose

Actions: Beta blocker with
mild alpha vasodilator effect

Contraindications: Asthma, chronic airways limitation

Side effects:
- Bradycardia
- bronchospasm
- headache
- nausea
- scalp tingling which usually
resolves within 24 hours

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13
Q

Explain the drug nifedipine in both the acute and ongoing context. Including the;
- dose
- actions
- contraindications
- practice points

A

Dose:
Acute: 10 mg tablet; max 40 mg
Onoging: 30mg or 60mg slow
release every 12 hours

Actions: calcium channel blocker/antagonist

Contraindications: aortic stenosis

Practice points:
- Severe headache in first
24 hours
- flushing
- tachycardia
- peripheral oedema
- constipation

Prescription:
- used in acute hypertensive situations
- may be used as a second line agent with labetalol or methyldopa

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14
Q

Define chronic hypertension

A

= Pre-existing hypertension that is a strong risk factor for the development of preeclampsia
and requires close clinical surveillance

Includes essential hypertension, secondary hypertension and white coat hypertension.

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15
Q

Define essential hypertension

A

= A systolic BP ≥ 140 mmHg and/or a diastolic BP ≥ 90 mmHg before pregnancy or before 20 weeks gestation without a known cause. It may include women presenting early in pregnancy on anti-hypertensive medications where no secondary cause for hypertension has been determined.
Considered chronic hypertension

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16
Q

Define secondary hypertension

A

= hypertension due to a condition such as;
- chronic kidney disease (e.g. glomerulonephritis, reflux nephropathy and adult
polycystic kidney disease)
- renal artery stenosis
- systemic disease with renal involvement (e.g. diabetes mellitus, systemic lupus erythematosus)
- endocrine disorders (e.g. phaeochromocytoma, Cushing’s syndrome and primary hyperaldosteronism)
- coarctation of the aorta
- medications.

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17
Q

Define white coat hypertension

A

= raised BP in the presence of a clinical attendant but normal BP in any other setting

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18
Q

What is the management of hypertension at A/N app?

A
  • ?signs and symptoms of pre-eclampsia
  • ?risk factors for pre-eclampsia and commence prophylaxis if present (150mg of aspirin daily, nocte + 1.5g calcium daily)

If sever hypertension
- follow hospital guidelines/previously discussed treatment of meds, FBC, NBM, crystalloid

If mild-mod
- ?first diagnosis or pre-existing
- ?medicated if pre-existing
Provide ongoing care of;
- Ophthalmic examination
- ECG (if not done recently)
- 24-hour urine catecholamines (if medicated)
- Urinalysis for proteinuria and spot urine PCR
- Serum electrolytes

Antenatal care – aim for BP <150/100
- Individualise schedule of antenatal visits
- 20 week US for morphology
- 28–30 weeks US for growth
- 30–32 weeks US for growth
- CTG if clinically indicated: e.g. abnormal fetal growth,
decreased fetal movement, unstable BP

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19
Q

What are some key practice point for antihypertensive therapy?

A
  • a BP ≥ 160/100 mmHg treatment is essential
  • mild-mod= Antihypertensive drug therapy is optional
  • Antihypertensive drug therapy confers no clear benefit to women with mild pre-eclampsia.
  • Lower blood pressure carefully, as inadequate placental perfusion may occur where placental circulation has adapted to a higher blood pressure.
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20
Q

Define pre-eclampsia

A

= A multi system disorder unique to pregnancy, characterised by hypertension and involvement of one or more organ systems and/or the fetus after 20 weeks’ gestation.
- resolves after delivery of the placenta, however, deranged blood values can take up to 3/12 to fully recover.

  • Proteinuria is a common, recognised additional feature after hypertension but is not a sign necessary for clinical diagnosis.
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21
Q

Define superimposed pre-eclampsia

A

= chronic hypertension that develops one or more of the systemic features of pre-eclampsia after 20 weeks of gestation.

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22
Q

Define eclampsia

A

= New onset Grand Mal Seizure in a pregnant woman with pre-eclampsia
- Cause unknown, lots of theories as to the cause.
- some suggest that seziures are a result of cerebral vasospasm and endothelial damage leading to cerebral ischaemia, microinfarctions and oedema.
- can occur antenatally, intrapartum and postnatally
- most commonly occurs 24hrs postnatally
- is not the most commonest cause of seizures in pregnancy and the differential diagnosis includes
epilepsy and other medical problems that must be considered carefully, particularly when typical features of severe preeclampsia are lacking.

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23
Q

Define HELLP syndrome?

A

= HELLP =Haemolysis, elevated liver enzymes, low platelets
- Life-threatening pregnancy complication considered to be a variant of pre-eclampsia
H: hemolysis= break down of RBCs
EL: elevated liver enzyme
LP: low platelet count
- Mortality rate 1 - 2%

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24
Q

What are the symptoms of HELLP syndrome?

A

*may at first seem like pre-eclampsia
- Headache
- Nausea and vomiting/indigestion with pain after eating
- Abdominal or chest tenderness ad upper right quadrant pain from liver distension
- Shoulder pain or pain when breathing deeply
- Bleeding
- Changes in vision
- Swelling
Signs to consi
- Epigastric (abdominal) or substernal (chest) pain, including abdominal or chest tenderness and upper right side pain (from liver distention)
- upper r) quadrant pain indicative of hepatic involvement.
- pain relief responds poorly
- Nausea, vomiting, or indigestion with pain after eating
- Headache that won’t go away, even after taking medication such as acetaminophen
- Shoulder pain or pain when breathing deeply
- Bleeding
- Changes in vision including blurred vision, seeing double, or flashing lights or auras
- Swelling, especially of the face or hands
- Shortness of breath, difficult breathing, or gasping for air

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25
Q

What are some diagnostic markers of HELLP syndrome?

A
  • High blood pressure
  • Protein in the urine
  • Abnormalities in laboratory blood work (increased liver enzymes, decreased platelets, and the presence of hemolysis)
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26
Q

What are some risk factors for developing HELLP syndrome?

A
  • preeclampsia and eclampsia
  • family history
  • family history of certain autoimmune conditions
  • family history of certain clotting disorders
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27
Q

What are the severity classes of HELLP syndrome?

A

= classified based on the blood test values which reflect the condition of the mothers blood vessels, liver and other organs.

Classes
*the lower class, the more dangerous the situation.
- Class I (severe thrombocytopenia): AST ≥ 70 IU/L, LDH ≥ 600 IU/L, platelets ≤ 50,000/uL
- Class II (moderate thrombocytopenia): AST ≥ 70 IU/L, LDH ≥ 600 IU/L, platelets > 50,000 ≤ 100,000/uL
- Class III (mild thrombocytopenia): AST ≥ 40 IU/L, LDH > 600 IU/L, platelets > 100,000 ≤ 150,000/uL

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28
Q

What is the significance of the platelets component of HELLP syndrome classing/diagnosis?

A

= (also known as thrombocytes) are colorless blood cells that help blood clot and stop bleeding by clumping and forming plugs in blood vessel injuries.
- Thrombocytopenia is a condition in which you have a low blood platelet count and is one of the defining characteristics of HELLP syndrome.

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29
Q

What is the treatment of HELLP syndrome?

A
  • delivery of baby and placenta
  • blood transfusions (sometimes with specifically RBC, platelets or plasma)
  • corticosteroids for fetal lung development in very preterm pregnancy
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30
Q

How can HELLP syndrome be prevented?

A
  • good physical health pre pregnancy
  • regular antenatal care
  • understanding of the warning and early signs
  • aspirin if at risk. Prevents pre-eclampsia and thus chnaces of developing HELLP syndrome.
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31
Q

What is the impact of HELLP syndrome on the baby?

A
  • if >1000g at birth appears to be no adverse long-term outcomes and same survival rates as non-HELLP babies.
  • <1000g at birth long hospital stays., increased chance of needing ventilator support
  • Placental abruption
  • Placental failure with intrauterine hypoxia/asphyxia
  • Extreme prematurity
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32
Q

Who are the three at-risk (based on a diagnosis) groups for hypertension?

A
  • pre existing primary hypertension
  • secondary chronic hypertension
  • those who develop new onset hypertension in the second half of pregnancy
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33
Q

When is transfer to a tertiary hospital indicated in the context of hypertension and pregnancy?

A
  • All pre-term pregnancies with severe pre-eclampsia, eclampsia or HELLP syndrome
  • All term pregnancies complicated by eclampsia or HELLP syndrome
  • Any pregnancy in which the health care provider believes his/her health care
    facility would be unable to manage the complications of hypertension in
    pregnancy.
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34
Q

What is the management of hypertension found in an antenatal setting?

A
  • recheck in 15mins
  • consult and refer to supporting hospital.
  • if >160 systolic or >100 diastolic reccomende ambulance transfer.
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35
Q

Explain the normal progression of blood pressure in pregnancy

A
  • falls in first trimester
  • reaching a nadir by the second trimester
  • rises again to pre-conception levels towards end of third trimester.
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36
Q

Define proteinuria

A

= urinary excretion of ≥0.3 g protein in a 24-hour specimen.
= ≥1+ reading on dipstick (must be with no evidence of UTI)

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37
Q

What are the 7 classifications of hypertension related conditions we must be aware of?

A
  • Preeclampsia – eclampsia
  • Gestational hypertension
  • Chronic hypertension
    - essential
    - secondary
    - white coat
  • Preeclampsia superimposed on chronic hypertension
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38
Q

How can pre-eclampsia be diagnosed?

A
  1. hypertension after 20wks
  2. accompanied with one or more of the following signs of organ involvement.
    Renal involvement
    - Significant proteinuria – a spot urine protein / creatinine ration > 30mg / mmol
    - Serum or plasma creatinine greater than or equal to 90 micromol/L or
    - Oliguria < 80mL / 4 hours
    Haematological involvement
    - Thrombocytopenia < 100,000 /µL
    - Haemolysis: schistocytes or red cell fragments on blood film, raised bilirubin, raised lactate dehydrogenase > 600mIU/L, decreased haptoblobin
    - DIC
    Liver involvement
    - Raised transaminases
    - Severe epigastric or right upper quadrant pain
    Neurological involvement
    - Convulsions (Eclampsia)
    - Persistent visual disturbances (photopsia, scotomata, cortical blindness,
    posterior reversible encephalopathy syndrome, retinal vasospasm)
    - Persistent, new headache
    - Stroke
    - Pulmonary oedema
    - Fetal growth restriction (FGR)
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39
Q

Define superimposed preeclampsia

A

= when a woman with pre-existing hypertension develops systemic features of preeclampsia, after 20 weeks gestation.
- Worsening or accelerated hypertension should increase surveillance for preeclampsia but is not diagnostic.

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40
Q

What are some risk factors for pre-eclampsia?

A

Moderate risk
- Age 40 years or more
- First pregnancy/nulliparity
- Multiple pregnancy
- Interval since last pregnancy of more than 10 years
- Body mass index of >35 at presentation
- Family history of pre-eclampsia
High risk
- Autoimmune disease e.g. Systemic Lupus Erythematosus (SLE), antiphospholipid syndrome
- Chronic hypertension
- Chronic kidney disease
- Hypertensive disease during a previous pregnancy
- Diabetes
- African American ethnic background
- PAPP-A <0.45 MoM
- Antiphospholipid syndrome

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41
Q

What is the management of new onset hypertension after 20wks gestation?

A
  • assess for signs and symptoms of pre-eclampsia
  • ?need to admit to unit
  • admit if preeclampsia symptoms are identified
42
Q

What is the management of eclampsia?

A
  • Resus
  • IV mag sulph (4g IV over 20mins loading dose)
  • if seziure occurring/ongoing while preparing mag sulf= diaz 5-10mg at rate of 2–5 mg/
    minute (maximum dose of 10 mg) or Clonazepam 1–2 mg IV over 2–5 minutes OR Midazolam 5–10 mg IV over 2–5 minutes or
    IM
  • maintenance dose of mag sulf of 1g IV via controlled induction live for 24/hr post birth.
  • if seziures continue with mag stuff then consider bolous or diasepam, midazolam or clonazepam.
    *note: if impaired renal function; reduce maintenance dose of magnesium sulfate to 0.5 g/hour and start O\ongoing serum monitoring
  • prevention of further sezirues
  • control of hypertension
    - do avoid hypo
    - nifedipine, hydralazine, labetalol, diazoxide
  • delivery

Monitor
- BP and pulse every 5 minutes until stable then every 30 minutes
- Respiratory rate and patellar reflexes hourly
- Temperature 2nd hourly
- Continuous ^CTG monitoring
- Measure urine output hourly via IDC
- Strict fluid balance monitoring
- Check serum magnesium if toxicity is clinically
suspected
- Therapeutic serum magnesium level 1.7–3.5
mmol/L

Stop function/review management when;
- Urine output < 80 mL in 4 hours
- Deep tendon reflexes are absent or
- Respiratory rate < 12 breaths/minute

43
Q

When is magnesium sulphate indicated?

A

= recommended for use antepartum, intrapartum and
within the first 24 hours postpartum for severe pre-eclampsia or in eclamptic episode for its anticonvulsant properties when the following factors are present:
- persistently elevated blood pressure despite adequate hypotensive therapy and appropriate fluid management,
- evidence of CNS dysfunction, thrombocytopenia or liver disease

44
Q

Define pre-eclamptic angina and what does it often indicate?

A

= Epigastric or right upper quadrant pain.
- often represents hepatic involvement

45
Q

What is the antenatal management of HELLP?

A
  • platelet transfusion pre-operative delivery
46
Q

What is the postpartum management of HELLP?

A
  • ?platelet transfusion if any bleeding related to pre-eclampsia thrombocytopenia
  • ?platelet transfusion in first 72hrs only if platelets fall below 40,000 despite no bleeding but there is a concern for bleeding e.g. after c/s
  • If the count remains below 40,000 after 72 hours from delivery without significant
    bleeding and without sign of impending recovery, consultation with the Consultant
    Haematologist or Obstetric Physician is indicated.
47
Q

What baseline assessments should be carried out on a women who presents with chronic hypertension?

A

Maternal
- Ophthalmic examination.
- Spot urine protein: creatinine ratio where there is doubt about proteinuria on dipstick, i.e., +1 or +2 proteinuria.
- Serum electrolytes.
- ECG (if not done recently).
- 24 hour urine catecholamines if there is severe hypertension.

Fetal
- Baseline ultrasound for the assessment of fetal anatomy.
- Follow-up ultrasound at 26-28 weeks.
- From 28 weeks, ultrasound every 2-3 weeks to evaluate fetal growth.
- Weekly non-stress tests from 30 weeks.

48
Q

Explain the post partum management of chronic hypertension

A
  • note it may be partcularly high on the 3rd-6th day after delivery so may need to increase or commence antihypertensive meds at that time.
  • blood pressure is unstable for 1-2 weeks after delivery and may be difficult to control
49
Q

What are some risk factors for preeclampsia?

A
  • previous Hx
  • antiphospholipid antibodies
  • pre-existing diabetes
  • multiple pregnancy
  • nulliparity
  • family history
  • elevated BMI >25
  • maternal age >40
    Diastolic BP >80mmHg at booking
  • chronic hypertension
  • pre existing renal disease
  • congenital heart defects
  • autoimmune disease
  • > 10 years since previous pregnancy
  • short sexual relationship prior to conception
  • other thromophilias
  • maternal ages <20 or >35 years
    maternal depression or anxiety
  • assisted reproduction tech
  • fetal triploidy
50
Q

What should be involved in pre-pregnancy counselling for those at sever risk of developing pre-eclampsia?

A
  • discussion of risk factors, symptoms and management
  • offer calcium and low dose aspirin supps
  • ?labetalol or methyldopa to optimise blood pressure
  • pre conception counselling
51
Q

What calcium should be offered in pregnancy and why?

A

= calcium supplements of 1200mg – 2000mg daily.
- seen to almost half risk of pre-eclampsia and reduces complications

52
Q

Explain the use of low-dose aspirin in those at risk of pre-eclampsia.

A

= those at risk should commence before or at 16wks and cease at 37wks.

53
Q

If the decision to expodite birth is made in the context of hypertension, what efforts to stabilise the situation pre-birth must be made?

A
  • control hypertension
  • correct coagulopathy
  • consider eclampsia prophylaxis
  • attention to fluid status
54
Q

What is used as an anecdote/reversal agent for mag sulf?

A

= 10% calcium gluconate 10 mL IV over 5-10 minutes
- requires ECG during administration due to risk of cardiac arrhythmias

55
Q

What are some key practice points to follow at the birth of a women with hypertension?

A
  • Actively manage third stage
  • Ergometrine should NOT be used in severe preeclampsia or eclampsia
  • Consider *carbetocin if increased risk
    of PPH
  • Consider VTE prophylaxis
56
Q

What are the first trimester screening options for those t risk of sever pre-eclampsia?

A

Placental growth factor (PlGF)
- Lowered levels in women at risk of pre-eclampsia15 and in fetal aneuploidies and/or impaired placentation2 disorders (which can also
be associated with pre-eclampsia)
- Positive predictive detection value of 56%15 for pre-eclampsia

Pre-eclampsia ratio test (PERT)
- measures proteins released from the placenta to assist in identifying women who will progress on to develop pre-eclampsia or not..

Uterine artery pulsatility index (UTPI)
- Measured between 11+0 and 13+6 weeks gestation15
- Positive predictive detection value of 48% for early onset preeclampsia

Pregnancy associated plasma protein A (PAPP-A)
- Levels less than 0.4 MoM, associated with an increased risk of HDP, preterm birth and fetal growth restriction34
- Present in 8–23% of women with pre-eclampsia15
- Low positive predictive detection value of 16%15

Combined first trimester screening
- VCGS offer testing called Early-Onset Pre-eclampsia (EO-PE) screening with a detection rate of 75%
- Blood is taken between 11-13.6 weeks measuring serum pregnancy-associated plasma protein -A (PAPP-A) and placental growth factor (PIGF) in maternal blood.
- u/s as well to assess placental blood flow.
*not covered by medicare
*these coupled with fam history and maternal BP=diagnosis

57
Q

What are the possible short and long term complication of hypertensive disorders?

A

Short term
- prem
- SGA
- admission to SCN
- stillbirth/death

Long term
- insulin resistance
- Diabetes melitis
- CAD
- hypertension
- increased risk of CVD
- overweight or oesity

58
Q

What are some indicators of fetal compromise in the context of hypertension?

A
  • reduced fetal movements
  • abnormal ctg
  • small amniotic deepest vertical pocket
  • low AFI
  • oligohydramnios
  • > 10th centile
  • fall in growth velocity
  • symmetrical vs asymmetrical growth
  • umbilical artery pulsatility >95centile
  • severe if absent or reversed end diastolic flow on umbilical artery
  • Ductus venosus doppler showing; Absent or reversed “a” wave or Identification of an abnormal ductus venosus waveform is not diagnostic in
    isolation when there is no other Doppler abnormality
  • middle cerebral artery showing cerebral redistribution
59
Q

What mode of birth is indicated for hypertension in pregnancy if it is indicated?

A
  • Recommend vaginal birth unless a caesarean section is required for other
    obstetric indications
  • If vaginal birth is planned and the cervix is unfavourable, recommend cervical
    ripening to increase the chance of successful vaginal birth
60
Q

Explain the drug hydralazine for ongoing treatment and acute treatment of hypertension. Including the;
- dose
- actions
- contraindications
- practice points

A

Dose:
Acute: 5–10 mg (first dose 5 mg if fetal compromise)
Ongoing: 25–50 mg tds

Action: Vasodilator

Contraindications

Practice points/side effects;
- Flushing, headache, nausea, lupus-like syndrome

61
Q

What is the necessary BP monitoring during the intrapartum phase for those with hypertension?

A

BP <160/110 mmHg – hourly BP measurement
BP ≥160/110 mmHg – continuous BP measurement.
Intrapartum analgesia

62
Q

At what gestation should the corticosteroid of betamethasone be considered at if sever hypertension/pre-eclampsia?

A

anything less than or qual to 36+3

63
Q

What are those with chronic hypertension and pre-eclampsia at risk for?

A
  • accelerated hypertension in the third trimester
  • superimposed pre-eclampsia
  • fetal growth restriction
  • placental abruption, premature delivery
  • stillbirth

Pre-eclampsia specific
- chronic hypertension
- ischaemic heart disease
- cerebrovascular disease
- peripheral vascular disease
- deep vein thrombosis
- end-stage renal disease
- type 2 diabetes
- elevated TSH
- all cancers

64
Q

What are signs of magnesium toxicity?

A
  • decreased deep tendon reflexes
  • respiratory rate <12 breaths per minute
  • reduced urine output: <40 mL per hour
  • serum magnesium concentration >3.5 mmol/L
65
Q

What is the necessary maternal observations during the use of mag sulf?

A

During loading dose:
- 5-minutely BP, pulse (PR) and respiratory rate (RR)
- at completion of loading dose, record BP, PR, RR and deep tendon reflexes
- observe for adverse effects.

During maintenance dose:
- hourly BP, PR and RR
- hourly urine output
- hourly deep tendon reflexes.

Maintain an accurate record of fluid balance.

Before discontinuing MgSO4 therapy:
- BP should be stable (consistently below 150/100)
- woman should have adequate diuresis
- woman should be clinically improved, with no headache or epigastric pain

66
Q

What are some key practice points in the post partum management of HELLP?

A
  • Daily obstetric review
  • 4-hourly observations for 48 hours:
    - vital signs
    - reflexes
    - clonus
  • Send the placenta for pathological examination and follow up results
  • Enalapril is the preferred antihypertensive agent:
    - 5 mg daily
    - can be used safely by breastfeeding mothers of term infants
    - exercise caution with breastfeeding mothers of preterm infants.
  • Hypertension may persist for up to three months and will require monitoring and slow withdrawal of antihypertensive therapy.
  • education
67
Q

Compare the drugs available for acute treatment of hypertension vs those used for maintenance/long term.

A

Acute: labetalol, nifedipine, hydralazine

Ongoing
1st line: labetalol and methyldopa
2nd line: hydralazine, nifedipine (if available) and prazosin
*multiple may be required

**all compatible with breast feeding

68
Q

What medication classes may make sense to use for hypertension, but are contraindicated in pregnancy?

A
  • Angiotensin converting enzyme (ACE) inhibitors
  • angiotensin receptor blockers (ARBs)

*3rd trimester use has been associated with FDIU and neonatal renal failure.
*can be used post partum and care computable with Breastfeeding

69
Q

What organ systems may be effected in pre-eclampsia and what may occur?

A

Renal involvement
- significant proteinuria - spot urine protein/creatinine ratio greater than or equal to 30mg/mmol
- Serum or plasma creatinine > 90 micromol/L
- Oliguria - < 80ml of urine over 4 hours

Haematological involvement
- Thrombocytopenia < 100 x 109/L
- Haemolysis
- DIC

Liver involvement
- Raised serum transaminases (AST and ALT >70IU/L
- Severe epigastric or right upper quadrant pain

Neurological involvement
- Convulsion/eclampsia
- Hyper-reflexia with sustained clonus (>3 beats)
- Persistent, new headache
- Persistent visual disturbances (photophobia, cortical blindness, posterior reversible encephalopathy syndrome, retinal vasospasm
- Stroke, usually haemorrhagic

Pulmonary oedema

Fetal growth restriction

70
Q

What is the intent behind prolonging a pre-eclamptic pregnancy?

A

= is of no benefit to the woman but may be a considered practice at early gestations to improve fetal outcome.
- thus is preeclampsia develops before 34wks delay birth 24-48hrs for administration of corticosteroids.

71
Q

What is the pharmacological management for those at a moderate to high risk of hypertension in pregnancy?

A
  • Low dose Aspirin 100-150mg from 16 weeks gestation, taken at night
  • 1.5 G calcium daily
72
Q

What are some complications of pre-eclampsia?
- maternal
- fetal
- neonatal

A

Maternal
- intercerebral haemorrhage
- placenta abruption
- eclampsia
- HELLp syndrome
- disseminated IV coagulation
- acute renal failure
- pulmonary odema
- acute respiratory distress
- ascites
- liver rupture
- eclampsia -1:200-300 women

Fetal
- FGR
- Oligohydramnios
- hypoxia from placental insufficiency
- placental abruption
- iatrogenic preterm birth
- FDIU

Neonatal
- all those associated with pre term birth
- hypoxia and neurological injury
- preinatal death

73
Q

Who should be involved in the multidisciplinary team treating a pt with acute preeclampsia?

A

Obstetrician
Midwife
Anaesthetist
Physician
Haematologist
Paediatrician

74
Q

What is the managements of a hypertensive pregnant person at;
- > or at 37wks
- <37wks
- <34wks

A

Management ≥37+0 weeks
- Birth is indicated
- Control BP as per Severe hypertension

Management <37 weeks
- Control BP – see Severe hypertension
- Prior to delivery:
- aim for BP <150/100
- optimise fluid status
- correct coagulopathy
- consider MgSO4 - See
- At ≥34 weeks, do not delay delivery as continuation of pregnancy is associated with risk to the fetus.

Management < 34 weeks
- Control blood pressure – see Severe hypertension
- At <34 weeks delivery should be delayed for 24–48hrs - if fetal and maternal status permit - to allow for administration of corticosteroids.

75
Q

When is Magnesium Sulfate (MgSO4) (Magnesium Sulfate Heptahydrate) indicated in the context of pregnancy hypertension?

A
  • for women with pre-eclampsia for whom there is concern about the risk of eclampsia
  • first-line management of an eclamptic seizure
  • first-line treatment of any seizure during pregnancy
  • neuroprotection of preterm infants
  • if diagnosis of sever pre-eclampsia is made

e.g. of clinical situation
- increased reflexes associated with clonus and/or severe headache, visual changes

76
Q

WHat are some key practice points of administering mag sulf?

A
  • 20ml/hr of urine output is inadequate
  • caution should be taken with any additional intravenous fluid administration to manage hypotension because of the potential risk of pulmonary oedema.
77
Q

What is the load and maintenance doses of mag sulf?

A

Loading dose:
- Using a 10mL vial of magnesium sulfate (10ml= 500mg/ml) prepare 4 gram (i.e. 8mL) of magnesium sulfate 50% in a 10mL syringe
- Configure the pump to accept the 10mL syringe and set the pump to 32mL/hr for 15 minutes

Maintenance dose:
- Once the loading dose has been completed, use the prepared 25g in 50mL magnesium sulfate syringe and re-set the pump to accept the 50mL syringe.
- Set the pump to administer the maintenance rate of 1g/hr (2mL/hr) or as ordered, until at least 24 hours post birth/delivery.

78
Q

What are some side effects of mag sulf?

A
  • hypotension secondary to reductions in systemic vascular resistance
  • facial flushing
  • visual disturbances
  • flushing at injection site
  • chest pain
  • nasal stuffiness
  • ECG changes
  • circulatory collapse
  • gastro-intestinal upset
  • urinary retention
  • magnesium toxicity
  • tissue necrosis at the injection site
79
Q

What are some contraindications of mag sulf?

A
  • caution in women being treated with cardiac
    glycosides/digitalis.
  • Concurrent use of magnesium sulfate and CNS depressants may result in an enhanced CNS depressant effect.
80
Q

What is the likely effect of the varying concentrations of mag sulf per mmol/L

A

0.8 - 1.0= normal plasma level
1.7 - 3.5= therapeutic range
2.5 - 5.0= ECG changes (P-Q interval prolongation, widen QRS complex)
4.0 - 5.0= reduction in deep tendon reflexes
> 5.0= loss of deep tendon reflexes
> 7.5= sinoatrial and atrioventricular blockade. Respiratory paralysis and CNS depression
> 12= cardiac arrest

Note: If serum magnesium level is >3.5mmol/L, cease infusion and consult with obstetrician

81
Q

What should the obs regimen be when administering mag sulf?

A

During administration of the loading or bolus dose:
- 5 minutely blood pressure and pulse (x 4 readings)
- observe for the development of side effects
- check patellar reflexes after administration

During administration of the maintenance infusion:
- ½ hourly blood pressure, pulse, and respiratory rate (pre-treatment respiratory rate should be ≥ 16per
minute). These may be undertaken hourly post-birth.
- 1 hourly patellar reflexes
- 1 hourly urine measures, 4 hourly testing of urinary protein
- 2 hourly temperature
- continuous electronic fetal monitoring from 26 weeks gestation until clinical review/discussion by medical staff. Between 24- 26 weeks gestation, individualised management with regard to fetal monitoring will be
considered
- maintain a strict fluid balance chart.

82
Q

What are some signs of mag sulf toxicity?

A
  • urine output <100mL in 4 hours
  • absent patellar reflexes
  • respiratory depression
83
Q

What are the main aspect of care for a women with sever pre-eclampsia?

A

Stabilise
- Control BP - IV Labetalol is the primary drug of choice for urgent control of severe hypertension in pregnancy. Hydralazine is the drug of choice for women with asthma or congestive heart failure.
- Prevent seizures using Magnesium Sulphate IV

Monitor
- vital signs
- urinary output
- neurological status
- clotting factors
- fetal condition

Plan for labour/birth
- The choice of either Caesarean section or Induction of labour is dependent upon:
- severity of the maternal disease
- gestational age
- fetal condition
- if the woman is in labour, consider epidural
- if the woman is in 2nd stage, consider expediting the birth.
- Consider thromboprophylaxis as pre-eclampsia is a risk factor for venous thromboembolism (VTE)
- Fluid management- this is closely monitored due to decreased urine output but risk of pulmonary oedema
- Strict fluid balance chart
- Oliguria is common with severe pre-eclampsia and in isolation does not require fluid replacement unless plasma creatinine is rising
- Hourly urine output measurements
- Limit fluids to 60-80ml/hr
- Timing of birth
- dependent on severity of maternal disease, gestational age and fetal condition
- prior to 34 weeks, aim to delay birth until administration of corticosteroids, if maternal and fetal condition permit
- consider Magnesium Sulphate for neonatal neuroprotection for women < 30 weeks gestation
- active 3rd stage management however DO NOT use Ergometrine or Syntometrine as routine oxytocics

84
Q

What monitoring should occur postnatally for a women with pre-eclampsia?

A
  • Daily obstetric review
  • 4-hourly observations for 48 hours:
    - vital signs and when BP is stable
    - reflexes
    - clonus
  • Send the placenta for pathological examination and follow up results
  • Magnesium sulphate should stop at a minimum of 24 hours post birth but as clinically indicated may continue beyond this time
  • Enalapril is the preferred antihypertensive agent:
    - 5 mg daily
    - can be used safely by breastfeeding mothers of term infants
    - exercise caution with breastfeeding mothers of preterm infants.
  • Slow withdrawal of anti-hypertensive medication and regular BP monitoring (may take up to 3 months for BP to stablise)
  • A diuresis has occurred and urine output has normalised (initially hourly IDC measurements)
  • FBE, LFT’s and U&E are stable/improving
  • After birth, all clinical and laboratory derangements of preeclampsia recover, but there is often a delay.
  • The woman and her family are often overwhelmed and distressed from their experience and appropriate counselling post-partum should include psychological and family support.
  • All women who develop pre-eclampsia and gestational hypertension are at risk of these disorders in future pregnancies and should receive appropriate counselling before embarking upon another pregnancy.
85
Q

WHat are some maternal and fetal complications of eclampsia?

A
  • coma
  • intracerebral haemorrhage
  • resp distress
  • perinatal death
86
Q

What is the first linea treatment for eclampsia?

A
  • Magnesium sulfate (MgSO4)
  • Diazepam is not an appropriate first line treatment.
87
Q

What are some signs of impending eclampsia?

A
  • sever frontal headache due to cerebral oedema
  • Hyperreflexia- impending eclampsia
  • Reduced urine output- renal failure
  • Blurred vision/visual disturbance- retinal oedema
  • Epigastric pain- due to haemorrhage in subcapsular layer of liver
  • Vomiting and nausea - due to cerebral oedema and liver damage
88
Q

What are the signs of an eclamptic episode?

A
  • generalised seizures with jerking limb and head movements
  • may be cyanosed
  • tongue biting
  • urinary incontinence
  • are generally single and self-limiting lasing less than 90 seconds
89
Q

What is the management of a prolonged seizure from ecalmpsia?

A
  • may be due to other intracerebral pathology, in which case benzodiazepines are appropriate:
    - intravenous diazepam (2 mg/min to maximum of 10mg)
    or
    - Midazolam (0.1 – 0.2 mg/kg IV or IM).
  • Urgent CT scan/MRI is recommended
90
Q

What is the management of eclampsia if birth is being planned?

A
  • Nil by mouth
  • 80ml/hr IV crystalloids
  • Continuous fetal monitoring is required whilst awaiting birth as there is no reason for delaying birth once an eclamptic seizure has occurred.
  • Prepare for Caesarean section if required.
  • Prepare for a potentially pre-term birth- Paediatrician informed and present at birth
  • If the woman is to birth, active 3rd stage of labour with Oxytocinon - DO NOT use Ergometrine or Syntometrine
91
Q

What documentation needs to occur in an eclamptic event?

A
  • Note the time the seizure occurred and its duration
  • Note the time of the emergency call and time of arrival of staff
  • Accurate documentation of all fluids administered and output
  • All observations and treatments to be documented
91
Q

What considerations need to be made regarding the women environment in the context of hypertension in pregnancy?

A
  • it is high enough acuity
  • is there adequate peads
  • Once the woman is stabilised, ongoing care should occur in a high dependency unit or intensive care unit with one on one care
  • High dependency level care should continue for 24-48 hours post seizure and if stable, then transfer to a Postnatal ward.
  • Enable the woman to spend time with her baby and encourage this
  • Support the woman with her feeding choices, commence expressing with the woman’s consent
  • Psychological support is paramount following a situation such as this.
92
Q

What is the main risk with HELLP?

A
  • expectant management is harmful with a 6.3% incidence of maternal death and an increased risk or placental abruption.
  • In such cases delivery should be planned as soon as feasible. (KEMH 2018)
93
Q

What are some maternal complications of HELLP syndrome?

A
  • Liver rupture
  • Cerebral oedema
  • Cerebral haemorrhage
  • Maternal death
94
Q

Define disseminated Intravascular Coagulation (DIC)

A

= an acquired syndrome characterized by the intravascular activation of coagulation (aka initiation of clotting) with a loss of localisation arising from different causes.
- It can originate from and cause damage to the microvasculature, which if sufficiently severe, can produce organ dysfunction
- always secondary to another underlying cause

  • Overproduction of thrombin leads to fibrin deposition and clots=
  • these microthrombi cause organ dysfunction
  • because of this massive clotting action the body becomes depleted of platelets
95
Q

What are the signs of DIC

A
  • thrombosis and/or bleeding as it is a thrombo-haemorrhagic disorder.
  • sever bleeding (PV, intrauterine, intraabdominal)
  • oozing from the skin/mucosa
  • shock
  • dyspnea, hemoptysis, acute renal failure
96
Q

What are some common primary complications that DIC can stem from?

A
  • Placental abruption (most common cause)
  • Amniotic fluid embolism
  • Pre eclampsia/HELLP syndrome
  • Retained stillbirth
  • Acute fatty liver of pregnancy
  • Severe infection
  • Massive bleeding (PPH, acreta)
  • septic abortion
97
Q

What results when DIC occurs?

A

= there is an excessive consumption of platelets and clotting factors resulting in:
- prolonged clotting time (prolonged prothombin time and partial thromboplastin time)
- low platelets (thrombocytopenia)
- low fibrinogen
- Raised D-Dimers
- haemorrhage

98
Q

Which professionals should be involved in the management of a pt with DIC early?

A

Haematology- to advise on appropriate blood products required to correct the clotting
Senior Obstetrician
Anaesthetic staff
Intensive care staff

99
Q

What is the management of DIC?

A
  • the cause should be investigated promptly and treated appropriately
  • Full blood examination
  • Cross- matching
  • Clotting profiles
  • Fibrinogen
  • Tranexamic acid (TXA) should be considered.