Mx - APH Flashcards

1
Q

What is antepartum haemorrhage and how commonly does it occur?

A

APH is defined as vaginal bleeding after 20 weeks gestation. It occurs in approx 2-6% of pregancies

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2
Q

What are the causes of APH?

A

placental abruption
placenta praevia
others - vasa previa, cervicitis, lower genital tract infection and malignancy

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3
Q

What are the risk factors for placental abruption?

A
previous abruption
hypertension or PET
smoking and drug use
trauma
PPROM
multiple pregnancy or polyhydramnios
ECV
thrombophilia
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4
Q

How does placental abruption present?

A

PV bleeding
Continuous abdo pain
Tender, firm (“wooden”) uterus -contracts in response to bleeding. A clinical dx - USS detects only 50%

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5
Q

What are the risk factors for placenta praevia?

A

advanced maternal age
previous C/S
smoking
multiparity

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6
Q

How does placenta praevia usually present?

A

Painless PV bleeding

Dx using USS

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7
Q

What are the key points for APH assessment?

A

1) Assessment - is the woman stable or is urgent intervention required? FMF and FHR?
2) If woman is stable - full history should be taken - nature and how much bleeding?
Painful? (placental abruption vs praevia),
SROM? (vasa previa)
Pap smear hx?
3) Exam - BP and HR, abdominal tenderness and rigidity, speculum examination - avoid VE if placenta praevia is possible.
4) Ix
- USS to dx placenta praevia
- FBC, Gp and hold
- Kleihauer test in Rh-neg to quantify FMH to gauge anti-D Ig dose
- Fetal - CTG

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8
Q

Which patients require admission?

A

Women with heavier than spotting, ongoing bleeding, unexplained APH or placental abruption should remain - mx is consultant led.

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9
Q

Pharmacological mx?

A

Steroids - 24-34 weeks gestation in case of imminent delivery
Anti-D Ig for Rh-negative women
Tocolysis - considered by consultant obstetrician

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10
Q

When and how should women with APH be delivered?

A

APH with fetal/maternal compromise - immediate delivery usually by C/S
If no compromise - senior obstetrician to establish timing and mode.
Continuous CTG is required in labour, with active mx of 3rd stage in anticipation of risk of PPH

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