Case 18 A 39-year-old woman with painful
vaginal bleeding at 37 weeks'
gestation
Mrs O'Neil, a 39-year-old woman, is brought into the
labour ward by ambulance at 37 weeks' gestation in her
fourth pregnancy. She gives a short history of sudden
onset worsening abdominal pain and bleeding per
vaginum.
What differential diagnoses would
you consider?
• Placental abruption
• Placenta praevia (see Case 17 )
• Early labour
• Other causes (e.g. cervical or vaginal polyps, cervical
ectopy)
• Unexplained
What history would you like to elicit
from this patient to help you formulate
a diagnosis?
Presenting complaints
• Nature and site of pain – is it constant or
intermittent?
• Amount and nature of bleeding – is it fresh and with
clots, exclude ‘ show ’ mixed with liquor?
• Fetal movements – are they present?
• History of problems in present pregnancy (e.g.
pre - eclampsia)
Past obstetric history
Details of previous pregnancies and labours including
complications such as placental abruption, placenta
praevia or intrauterine growth restriction.
Past medical, personal and social history
• Cervical smear history
• History of hypertension
• Smoking or cocaine use
Mrs O'Neil had been feeling somewhat off colour for the
past day or so, although prior to that her pregnancy had
been uneventful. Earlier today she experienced worsening
abdominal pain along with a small amount of dark red
vaginal bleeding. She feels this pain is different from her
previous labours as it was constant and did not feel like
uterine contractions. She had not felt her baby move since
the pain set in.
She has had three uneventful pregnancies all resulting in
vaginal deliveries at term. In her present pregnancy, she
booked at 18 weeks and has seen her midwife on two
occasions as documented in her handheld notes. She
smokes 25–30 cigarettes every day but denies substance
abuse and lives in a council house with her three children.
What key signs would you look for
during the physical examination?
General examination
Check for pallor. Take her pulse and blood pressure.
Abdominal examination
Check the symphysiofundal height, fetal lie and presentation. If uterine contractions are present, what is their
strength, duration and frequency. Is the uterus relaxing
well between contractions?
Check for tenderness on abdominal palpation. What
is the tone of the uterus between contractions (i.e. is it
soft, or hypertonic/hard/woody)?
Assess the fetal heart rate.
Mrs O'Neil is pale and in obvious pain. Her pulse is 132
beats/minute and her BP is 90/60mmHg. The uterine height
is appropriate for gestation, although it is difficult to
ascertain the fetal lie as her uterus feels woody hard and is
tender to touch. The midwife is unable to pick up the fetal
Obstetrics and Gynaecology: Clinical Cases Uncovered.
By M. Cruickshank and A. Shetty. Published 2009 by Blackwell
Publishing. ISBN 978-1-4051-8671-1.122 Part 2: Cases
PART 2: CASES
heart on Doppler ultrasound or cardiotocography (CTG).
There is minimal dark red blood loss per vaginum.
Now let us reconsider the diagnosis
on the basis of the information
available
Mrs O ' Neil ' s history and clinical examination are highly
suggestive of mixed type placental abruption leading to
Box 18.1 Placental abruption
This occurs in approximately 1 in 80 deliveries
Definition
The partial or complete premature separation of the
placenta prior to the birth of the baby
Risk factors
• Increasing maternal age and/or parity
• Low socioeconomic group
• Smoking or cocaine use
• Hypertensive disorders
• Sudden uterine decompression (e.g. rupture of
membranes with polyhydramnios)
• Severe external trauma
• Uterine abnormality, short cord
• Previous history of abruption. Recurrence rate is 7–9%
Symptoms
• Abdominal pain – usually constant and severe with
backache
• Vaginal bleeding – may be old or fresh blood
• Reduced or absent fetal movements
Signs
• Shock out of proportion to blood loss
• Spasm of uterus – described as ‘woody’ – from
hypertonic contractions
• Tender uterus
• Fetal parts difficult to feel
• Often no fetal heart
• Rarely may present as idiopathic preterm labour
Classification
• Concealed: blood trapped between the placenta and
uterine wall, no external bleeding
• Revealed: blood tracks between the membranes and
uterine wall with external bleeding from placenta edge
separation
• Mixed: combination of both types
Box 18.2 Pathophysiology of placental
abruption
• Placental abruption arises from haemorrhage into the
decidua basalis of the placenta
• Expanding haematoma leads to separation of adjacent
placenta with or without vaginal bleeding and fetal
distress or demise
• Bleeding may be concealed wholly or in part
• Bleeding into the amniotic sac leads to bloodstained
liquor
• Bleeding may infiltrate into the myometrium, tracking to
the serosa and resulting in the appearance of a
Couvelaire uterus
• Sustained uterine contraction is thought to be the result
of intramyometrial bleeding and the release of
prostaglandins
shock and intrauterine fetal death as the cause for her
antepartum haemorrhage (APH) (Boxes 18.1 & 18.2 ; Fig
18.1 ). The other common cause of APH, placenta praevia,
is usually associated with a painless APH in which the
shock is in proportion to the external bleeding. Also, as
the bleeding is maternal, the fetus is usually in good
condition. This is therefore an unlikely diagnosis in Mrs
Smith ' s case.
What are the complications associated
with placental abruption?
Placental abruption is a condition frequently associated
with serious maternal morbidity and high perinatal morbidity and mortality (Box 18.3 ).
What would be the next step in the
management of the mother?
Resuscitation of the mother
• Call for help from the senior obstetrician, anaesthetist
and midwifery staff
• Check airway, breathing and circulation (ABC) and
give oxygen. Insert two large - bore intravenous cannulae
and start fluid resuscitation by crystalloid or colloid (Box
18.4 )
• Determine the patient ' s rhesus status and cross - match
blood (4 – 6 units)
• Alert porters, laboratories and the blood bank
• Obtain blood for a full blood count, biochemistry
(urea and electrolytes, serum creatinine and urate, liver
function tests) and coagulation screenCase 18 123
PART 2: CASES
External abruption Relatively concealed abruption Concealed abruption
Figure 18.1 Concealed, revealed and mixed types of placental abruption.
Box 18.3 Complications of placental abruption
• Hypovolaemic shock
• Disseminated intravascular coagulation
• Postpartum haemorrhage
• Renal failure
Fetal complications
• Fetal distress
• Intrauterine fetal death
• Preterm delivery
• Perinatal mortality: 300/1000
KEY POINT
Treatment is aimed at treating the shock and preventing
disseminated intravascular coagulopathy (DIC).
Mrs O'Neil is managed as an obstetric emergency in the
high dependency area of the labour ward. Immediate help is
summoned and resuscitation commenced by giving facial
oxygen and inserting two 14-gauge cannulae for fluid
administration. Blood samples are obtained for urgent
cross-match and relevant investigations and a urinary
catheter inserted for output monitoring.
Intrauterine fetal death is confirmed by an onsite scan.
The scan also confirmed partial separation of an anteriorly
placed placenta by a large retroplacental clot.
Box 18.4 General management principles of
obstetric emergencies
• Manage airway, breathing and circulation
• Remember, there are two patients – the mother and the
fetus (although in this case there has been intrauterine
fetal death)
• The fetus is vulnerable to maternal hypoxia
• Consider invasive monitoring (e.g. central or arterial
line)
• Insert a urinary catheter for monitoring output and
check for proteinuria
• Replace blood and blood products as required
Assess fetal health
Assess by ultrasound and CTG if the fetus is alive. Check
fetal heart and lie and begin continuous fetal CTG. Also,
look for the presence of retroplacental clot, which is not
always evident on the scan, and confirm that the placenta
is not low lying.
Delivery of the fetus
If the fetus is alive, the decision regarding the mode of
delivery depends upon presence or absence of fetal
distress, and the amount of haemorrhage. A caesarean
section may be indicated for fetal or maternal reasons
(e.g. deterioration of maternal condition, fetal distress
as confirmed by CTG). If the fetus is not distressed,
induction or augmentation of labour with artificial
rupture of membranes with or without oxytocin infusion
may be attempted with the aim of a vaginal delivery;
however, the fetal condition must be closely and continuously monitored by CTG. If the fetus is dead, induction of labour may be performed if maternal condition
allows.
Women with severe abruption usually labour spontaneously and tend to have short labours.124 Part 2: Cases
PART 2: CASES
A vaginal examination is performed which reveals that
Mrs O'Neil is in labour and her cervix is 4cm dilated. An
amniotomy (artificial rupture of membranes) is performed
and an infusion of Syntocinon commenced to expedite
delivery. Liquor is noted to be bloodstained, consistent with
the diagnosis of placental abruption.
Mrs O'Neil's condition remains stable over the next 20
minutes and the uterine contractions become more regular.
Soon thereafter she delivers a fresh stillborn fetus weighing
3320g. The placental delivery was followed by the passage
of 950g of old clots, confirming the diagnosis of placental
abruption.
What would you watch out for
after delivery?
Abruption increases the risk of atonicity of the uterus and
postpartum haemorrhage (PPH). PPH can worsen or
cause DIC.
Following the completion of the third stage of labour, the
emergency buzzer is set off, as there is significant atonic
PPH. Help is summoned and the haemorrhage is controlled
by bimanual uterine compression and the administration of
oxytocics. While the resuscitation is being carried out the
anaesthetist notices that there is excessive oozing from the
venepuncture sites along with significant bruising of her arm
along the blood pressure cuff site, and haematuria. He
suspects that DIC has set in and alerts the resuscitation team
to the possibility. The on-call haematologist confirms the
diagnosis of DIC.
The International Society on Thrombosis and Haemostasis defines DIC as: ‘ An acquired syndrome characterized by the intravascular activation of coagulation with
loss of localization arising from different causes. ’
With placental abruption, decidual fragments containing activated coagulation factors enter the maternal circulation. DIC in abruption is caused by enhanced and
sustained abnormal generation of thrombin by intrinsic
pathways of coagulation.
What are the diagnostic tests for DIC?
DIC is primarily a clinical diagnosis; laboratory tests
are used to confirm the diagnosis and monitor replacement of blood components. No one test can diagnose
DIC.
Tests for DIC
• Platelet count ↓
• Prothrombin time ↑
• Thrombin time usually ↑
• Activated partial thromboplastin time ↑
• Fibrinogen ↓
• Fibrinogen degradation products
• Microangiopathic changes on peripheral smear
How will you manage Mrs O'Neil, who
has now developed DIC secondary to
placental abruption?
• Continue to manage ABC
• Mainstay of management is to treat the underlying
cause (e.g. if still undelivered, expedite delivery)
• Manage in consultation with a haematologist
• Laboratory tests dictate the need for blood, fresh
frozen plasma, clotting factors replacement and platelet
transfusion
Mrs O'Neil is managed by a multidisciplinary team
comprising a consultant obstetrician, consultant anaesthetist
and consultant haematologist along with supporting staff in
a high dependency setting. Fluid replacement is guided by
invasive monitoring, urine output and infusion of Syntocinon
is used to maintain uterine contractility.
Packed red cells, fresh frozen plasma and cryoprecipitate
are administered and over the next few hours her clinical
condition stabilizes and her coagulation profile improves.
She is monitored intensively for 24 hours with frequent
relevant investigations.
She is then transferred to a single room in the postnatal
ward caring for women with pregnancy loss. The following
day a debriefing session is undertaken to go through the
events and answer any questions. She is discharged home
on day 4 following delivery, with a date for postnatal
follow-up at the counselling clinic 6 weeks post delivery.Case 18 125
PART 2: CASES
CASE REVIEW
This 39 - year - old parous woman presented at 37 weeks '
gestation in shock with a history of painful APH and loss
of fetal movements. Her age, parity, smoking history and
socioeconomic status place her at risk for placental
abruption. Her history of constant abdominal pain,
vaginal bleeding and the findings of a tender woody
uterus along with fetal demise are highly suggestive of
the diagnosis of placental abruption.
The mainstay of management is adequate resuscitation
of the mother. The guidelines for managing major
obstetric haemorrhage recommend that two peripheral
lines should be set up using at least 14 - gauge cannulae
and blood cross - matched for 6 units. Plasma expansion
should be provided by colloids.
The next step is to expedite delivery of the fetus, the
mode of which depends upon gestation, fetal well - being
and maternal condition. If the mother ' s condition is
stable and the fetus is in good condition, induction of
labour is appropriate, as women with abruption usually
have a quick short labour.
Following delivery, PPH and DIC are the major
complications to watch out for.
• Multidisciplinary team involvement is strongly
recommended
• Resuscitation of the mother and early delivery of the
fetus are the mainstay of management
• PPH and DIC are serious complications to watch out for
KEY POINTS
• Placental abruption is an important cause of maternal
morbidity and perinatal morbidity and mortality
• Differential diagnosis is mainly from placenta praevia and
labour
• APH with sustained painful uterine contractions in the
presence of a tender uterus and fetal distress or demise
should alert one to the diagnosis
Further reading
Baskett TF , Arulkumaran S . Antepartum haemorrhage . Intrapartum Care for the MRCOG and Beyond. RCOG Press . 2002 ;
133 – 141 .
Hl - adky K , Yankowitz J , Hansen WF . Placental abruption . Obset
Gynecol Surv 2002 ; 57 : 299 – 305 .
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