APH Flashcards

1
Q

Define APH

A

RCOG defines this as bleeding from or into the genital tract occurring in the period from 24 weeks gestation up to the birth of the baby. Revealed or concealed therefore vigilance is required for signs of shock.

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2
Q

Incidence rate

A

3-5% of pregnancies

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3
Q

Causes of APH

A

Placenta previa
Placental Abruption
Placenta Accreta/percreta /increta
Varicosities/polyps or trauma

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4
Q

3 categories

A

Spotting/ minor <50 mls
Major 50-1000mls
Massive >1000mls or signs of clinical shock

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5
Q

Risk Factors

A
Previous APH
Previous Abruption/ previa
Substance misuse
Grand multiparity
Pre-eclampsia/ PIH 
Intrauterine infection
Polyhydramnious
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6
Q

Placental Abruption

A

Is the complete or partial detatchment of the placenta from the uterine wall prematurely. Trauma or spontaneously. 10x more likely if history of placental abruption. Increased risk of abruption with hypertension and chorioamniotitis.

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7
Q

Symptoms of Placental abruption

A

Bleeding can be overt or concealed.
Continuous abdominal pain continuous in back or side.
Palpation should be avoided but on gentle palpation tense/rigid and large on palpation. Difficult to feel fetal parts. Pathological CTG and Shock.

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8
Q

Placenta previa

A

Placenta implant in the lower part of the uterus close to or over the cervical os. Blood loss is never concealed,
Low lying (not occluding os)
Marginal (occlusion could occur)
Partial (partial occlusion of cervix)
Total (cervix is completely covered by it)
DO NOT VE UNTIL PREVIA IS RULED OUT WITH USS

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9
Q

Placenta accreta/increta or percreta

A

Placenta is embedded in the uterine wall. Detected on USS.

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10
Q

Why is quick intervention important?

A

Normal physiological changes in pregnancy mean women are likely to compensate longer but deteriorate quicker and lose blood rapidly. >1000mls lose ability to compensate.

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11
Q

Potential outcome of APH

A

Hypovolaemic shock > loss of blood > decreased circulatory volume > decreased oxygen perfusion> anaerobic respiration> cell dysfunction> increased lactate, low pH> SIRS> MODS> Death

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12
Q

What is there an increased risk of with APH?

A

Increased risk of PPH, anaemia and infection. Little reserves following APH for compensation. If MOH risk of coagulopathy and MODS.

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13
Q

What should we prepare with APH?

A

Resuscitaire for NNR.
IUGR.
Premature delivery.
HIE as a result of Hypoxia

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14
Q

What history is useful for APH?

A

Coagulopathy? USS? Trauma? Prev APH or Abruption? How much loss? Colour of loss? is it clotting? Fetal Movements? Rapid dilatation? Any pain?

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15
Q

Rh Neg?

A

Take Kleihauer bloods to calculate dose of Anti D.

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16
Q

What bloods would we need?

A
FBC (Hb &amp; PLT (DIC)) 
Us&amp;Es (kidney function)
LFTs (Liver function)
Clotting Studies (DIC?) 
Group and Save (Crossmatch 4 units)
17
Q

Initial Management

A

ABCDE O2 15l/min with non rebreathe mask
2x 16G cannulas (early access as peripheral veins with collapse in hypovolaemic shock)
Begin continuous monitoring with Dynamap and baby on CTG.
Catheterise using ANTT with foley indwelling catheter with urometer and fluid balance to prevent pulmonary oedema due to potential decreased kidney function.

18
Q

How to identify cause?

A

USS to rule out placenta previa & abruption.

Once previa is ruled out, further vaginal examination can be undertaken to assess dilatation etc.

19
Q

Further intervention

A

? expedite delivery, prepare for theatre.
May subside/stabilise.
?preterm corticosteroid e.g. dexamethasone
Prepare for NNR.
Cord Bloods.
Active 3rd stage recommended. 1:1 care on CDS ?ITU/HDU
Repeat bloods at 6 and 12 hours to observe Hb and PLT.
Adjust VTE
?SCBU/ HYPO pathway.
BFS, Pain relief, VTE adjusted, TWOC.
Document, DATIX, Debrief.