Obstetrics Flashcards

1
Q

What is the mortality of an amniotic fluid embolism?

A

20%

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2
Q

What is the incidence of AFE?

A

1/8,000 to 1/80,000

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3
Q

When does a presentation of AFE typically occur?

A

During labour or within 30 minutes of delivery

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4
Q

What are the core features of AFE? (4)

A

Bronchospasm
Pulmonary hypertension
Left ventricular failure
Coagulopathy

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5
Q

What are the most common presenting features of AFE?

A

Aura (restlessness, agitation, numbness) - 30%
Dyspnoea - 20%
Acute foetal compromise - 20%
Hypoxaemia
Hypotension

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6
Q

What are the most common features of AFE?

A

Maternal haemorrhage - 65%
Hypotension - 63%
Shortness of breath - 62%
Coagulopathy - 62%
Aura - 47%
Foetal compromise - 43%
Cardiac arrest - 40%
Cardiac dysrhythmias - 27%
Seizures - 20%

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7
Q

How is a diagnosis of AFE confirmed?

A

It is a clinical diagnosis, however it can only be confirmed on post mortem examination of the pulmonary vessels containing foetal squames and hair

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8
Q

What are the likely biochemical results of AFE?

A

↓ fibrinogen
↓ platelets
↑ fibrin degradation products
↑ APTT
↑ PT

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9
Q

Why is cryoprecipitate of particular use in AFE?

A

Cryoprecipitate containsfibronectinwhich activates thereticuloendothelialsystem and helps to filter antigenic material, and contains fibrinogen which is low in AFE

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10
Q

Which sensory nerve roots are responsible for transmitting the pain of the 1st stage of labour?

A

T10-L1

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11
Q

Which sensory nerve roots are responsible for transmitting the pain of the 2nd stage of labour?

A

S2-S4

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12
Q

What are the advantages of a PCEA bolus regimen

A

Improved satisfaction
Reduced staff resources
Potentially lower motor block

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13
Q

What is a standard regimen for a remifentanil PCA for labour analgesia?

A

0.3-0.5 mcg/kg 2-3 min lockout
Usually 40 mcg bolus

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14
Q

Define pre-eclampsia

A

Disorder of pregnancy:
- New-onset hypertension (systolic blood pressure ≥140 mmHg and/or a diastolic blood pressure ≥90 mmHg)
- After 20 weeks’ gestation

Although often accompanied by new-onset proteinuria, it may present in the absence of proteinuria in some women

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15
Q

Define severe pre-eclampsia

A

Pre-eclampsia with severe hypertension and/or
with symptoms,
and/or
biochemical,
and/or
haematological impairment

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16
Q

Mild hypertension

A

SBP 140-149mmHg
DBP 90-99mmHg

17
Q

Moderate hypertension

A

SBP 150-159mmHg
DBP 100–109mmHg

18
Q

Severe hypertension

A

SBP > 160mmHg
DBP > 110mmHg

19
Q

Symptoms of pre-eclampsia?

A

Severe headache
Problems with vision, such as blurring
Severe pain just below the ribs
Vomiting
Sudden swelling of the face, hands or feet

20
Q

Which patients are at increased risk of pre-eclampsia?

A

Hypertensive disease during a previous pregnancy
Chronic hypertension
Type 1 or 2 diabetes
Chronic kidney disease
Autoimmune disease such as SLE or antiphospholipid syndrome

21
Q

What is the proposed therapy for those at increased risk of pre-eclampsia?

A

Aspirin daily 75 mg

22
Q

What is the success rate of epidural blood patch?

A

50-80%

23
Q

Differential diagnosis for PDPH

A

Simple tension headache
Migraine
Venous sinus thrombosis
Intracranial haemorrhage
Intracranial mass
Pre-eclampsia
Meningitis

24
Q

What is the procedure for epidural blood patch?

A

Most senior anaesthetist
Strict asepsis
20 mL blood - stop if pressure/pain
Lie supine for 2 hours
Gradually mobilise
Follow up 2 hour, 24 hours, 1 week, 1 month

25
Q

Management of seizures in LA toxicity

A

Benzodiazepine, thiopental or propofol in small incremental doses

26
Q

What should you do to follow up LA toxicity?

A

Transfer to appropriate clinical area (ITU)
Exclude pancreatitis by clinical review, daily amylase/lipase for 2 days
Report cases to the NPSA
Document lipid use at lipidregistry.org

27
Q

What are the doses of intralipid during LA toxicity

A

1.5 ml/kg over 1 min of 20% lipid emulsion
Start infusion of 15 ml/kg/hr
Give up to 2 rpt boluses
Double infusion to 30 ml/kg/hr
Maximum cumulative dose of 12 ml/kg

28
Q

When is the peak time for teratogenicity of anaesthetic agents?

A

Week 3-8 gestation
21-56 days

29
Q

What are the treatment options for severe PET?

A

Labetalol (Oral/Infusion)
Hydralazine IV
Oral Nifedipine
Magnesium
Fluid Restrict
Expedite Delivery

30
Q

What are the features of an epidural haematoma?

A

Back pain: often severe and local, and can radiate to the arms or legs
Weakness: progressive weakness in the lower extremities, often bilateral
Paraesthesias: numbness or other sensory deficits in the lower extremities
Bowel and bladder dysfunction
Pain when pressure is applied: can be aggravated by direct pressure on the spine, coughing, sneezing, or straining

31
Q

Phase 1 of AFE

A

Phase 1 (~30 mins)
Amniotic fluid + foetal cells enter maternal circulation
Release of biochemical mediators
Pulmonary artery vasospasm → pulmonary hypertension
Elevated right ventricular pressures + right ventricular dysfunction
Hypoxaemia + hypotension
Myocardial and capillary damage

32
Q

Phase 2 of AFE

A

Phase 2 (if phase 1 survived)
Left ventricular failure
Pulmonary oedema
Biochemical mediators trigger DIC → massive haemorrhage + atony

33
Q
A