2.3 Amniotic Fluid Air Embolism Flashcards
A 37-year-old female who is 30 minute postpartum with an epidural
suddenly becomes short of breath and is worsening.
What are the causes of shortness of breath in pregnancy?
Patient factors
* Asthma
* Pulmonary infection
* Anaemia
Obstetric factors
* Pre-eclampsia
* Amniotic fluid embolism (AFE)
* Pulmonary embolism
* Ergometrine use
* Cardiomyopathy
Anaesthetic factors
* High block assuming that the epidural is still being used in this case
Another way to classify the differential diagnoses is to take the obstetric
versus nonobstetric approach.
What is the pathophysiology of AFE?
First described by Steiner in 1941,
it is a diagnosis of elimination after other causes of
cardiovascular instability and collapse have been rejected.
Difficult diagnosis is reflected by a wide ranging incidence of
1:8000 to 1:80 000 deliveries
Pathogenesis
- Embolic:
due to an emboli caused by entry of
amniotic fluid or fetal cells in the circulation
- Embolic:
- Immunological:
similar to anaphylaxis as fetal cells are not always present
- Immunological:
Presentation
- Occurs usually during labour and delivery
(including LSCS) but can occur
up to 48 hours post delivery, typically in two phases
. - Phase 1:
characterised by acute shortness of breath and hypotension
followed by cardiac failure,
cardiac arrest,
pulmonary oedema,
acute lung injury, convulsions. and loss of consciousness.
The maternal mortality rate is 26%–60%. - Phase 2: 40% of women who survived the first stage will go on to develop
the haemorrhagic phase due to DIC.
What are the risk factors for AFE?
No proven risk factors,
but the following may be associated with a higher risk
of developing AFE:
Advanced maternal age,
multiparity,
meconium stained liquor,
intrauterine fetal death,
polyhydramnios,
strong frequent or tetanic uterine contractions,
microsomia,
chorioamnionitis,
uterine rupture,
and placenta accreta.
What systemic changes occur during AFE?
- Haemodynamic changes
* Increase in systemic and pulmonary vascular resistance,
resulting in acute pulmonary hypertension,
left ventricular dysfunction and pulmonary oedema.
- Myocardial dysfunction results from ischaemia
and as a direct depressant
effect of endothelin and humoral factors.
- Pulmonary
* Vasospasm and ventricular dysfunction lead to hypoxia.
- Survivors develop an ARDS-like picture.
- Coagulation.
- DIC
- Amniotic fluid contains activated coagulation factors II, VII, and X. It
induces platelet aggregation, releases platelet factor III, and has a
thromboplastin-like effect. - The clinical picture is one of massive haemorrhage and haemodynamic
collapse.
What is the management of AFE?
The management is mainly supportive,
invasive monitoring,
and transfer to ITU.
Management goals in the operating theatre are
- Maintaining oxygenation—use of PEEP.
- Haemodynamic stability—inotropes are usually required.
- Maintenance of uterine tone.
- Management of DIC—
Liaise with haematologist. FFP, cryoprecipitate, and
platelets are usually required.
Recombinant factor VII has been used in
massive haemorrhage.