Puerperium Flashcards

1
Q

Define primary post-partum haemorrhage

A

Loss of > 500ml of blood per-vagina within 24 hours of delivery

  • minor = 500-1000
  • major = > 1000
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2
Q

Aetiology of primary PPH

A

Tone - uterine atony is most common cause
- maternal profile - age>40, BMI > 35, Asian ethnicity
- uterine overdistention - multiple pregnancy, polyhydramnios, foetal macrosomia
- labour - induction, prolonged
- placental problems - placenta praevia, placental abruption, previous PPH
Tissue
- retained placental tissue
Trauma
- instrumental delivery
- episiotomy
- c-section
Thrombin
- vascular - placental abruption, hypertension, pre-eclampsia
- coagulopathies

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3
Q

Clinical features of primary PPH

A

Bleeding per vagina

Dizziness, palpitations SOB

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4
Q

Investigations for primary PPH

A
FBC
Cross match 4-6 units
Coagulation profile
U+E
LFTs
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5
Q

Management of primary PPH

A

Immediate

  • resuscitation
  • involve whole team
  • investigations and monitoring
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6
Q

Definitive management of primary PPH

A

Uterine atony
- bimanual compression to stimulate uterine contraction
- pharmacolgical measures
- intrauterine balloon, haemostatic suture, hysterectomy
Trauma
- repair of primary laceration
Tissue
- IV oxytocin, manual removal of placenta with regional or GA
Thrombin
- correct with blood products under advice of haemotolgy

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7
Q

Drugs used in primary PPH

A

Syntocinon
- synthetic oxytocin - act on receptors in myometrium
- SE = N+V, headache, rapid infusion, hypotension
- CI = hypertoninic uterus, severe CVS disease
Ergometrine
- multiple receptor sites
- SE = hypertension, nausea and bradycardia
- CI = hypertension, eclampsia, vascular disease
Carboprost
- prostaglandin analogue
- SE = bronchospasm, pulmonary oedema, HTN, cardiovascular collapse
- CI = cardiac disease, pulmonary disease
Misoprostol
- prostaglandin analogue
- SE = diarrhoea

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8
Q

Prevention of primary PPH

A

Active management of 3rd stage of labour

- 5-10 units IM/IV oxytocin

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9
Q

Define secondary post-partum haemorrhage

A

Excessive vaginal bleeding in period from 24 hours after delivery to 12 weeks postpartum

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10
Q

Risk factors for secondary PPH

A

Uterine infection - endometritis
- risk factors include C-section, premature rupture of membranes and long labour
Retained placental fragments or tissue
Abnormal involution of placental site
- inadequate closure and sloughing of spiral arteries at placental attachment site
Trophoblastic disease

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11
Q

Clinical features of secondary PPH

A

Excessive vaginal bleeding

- spotting on and off with occasional gush of fresh blood

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12
Q

Investigations for secondary PPH

A
FBC
U+Es
CRP
Coagulation profile
G+S
Blood cultures
USS pelvis - retained placental tissue
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13
Q

Management of secondary PPH

A

Antibiotics - ampicillin and metronidazole
Uterotonics - syntocinon, carboprost and misoprostol
Surgical if excessive of continuing - insertion of balloon catheter

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14
Q

Features of depression during pregnancy

A
Low mood
Lethargy
Anhedonia
Poor sleep and appetite
Worries about childbirth and caring for baby
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15
Q

Management of depression during pregnancy

A

Social support and psychological treatments

Seek specialist advise before prescribing antidepressants

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16
Q

Define postnatal depression

A

Depressive episode within the first 12 months postpartum

- peak incidence is during first 2 months

17
Q

Features of postnatal depression

A

Similar to those of depression

- negative cognitions about motherhood and coping skills

18
Q

Management of postnatal depression

A

Mild - CBT and support groups
Severe - specialist team involved, TCAs, SSRIs
Pharmacological management depends on whether breastfeeding

19
Q

Define Puerperal Psychosis

A

Develops rapidly

Starts within days to weeks of delivery

20
Q

Features of puerperal psychosis

A
Manic/severe low mood
Rapid changes in mood
Confusion
Issues with sleep
Racing thoughts7Hallucinations
Delusions
21
Q

Management of puerperal psychosis

A

Generally require admission to specialist unit - high risk of suicide and infanticide
CBT
ECT
Medications - SSRIs, TCAs, mood stabilisers, antipsychotics