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D R . T H E I N T W A I P H Y O
P G 3 , E M
Antepartum Haemorrhage
 Antepartum haemorrhage (APH) is defined as
bleeding from or in to the genital tract, occurring
from 24+0 weeks of pregnancy and prior to the birth
of the baby.
 The most important causes of APH are placenta
praevia and placental abruption.
 APH complicates 3–5% of pregnancies
 leading cause of perinatal and maternal mortality
worldwide
 Up to one-fifth of very preterm babies are born in
association with APH
Severity
 NO consistent definitions of the severity of APH. It is
recognised that the amount of blood lost is often
underestimated
 The amount of blood coming from the introitus may
not represent the total blood lost (for example in a
concealed placental abruption).
 It is important to assess for signs of clinical shock
 The presence of fetal compromise or fetal demise is
an important indicator of volume depletion
Different terminology used
 Spotting – staining, streaking or blood spotting
noted on underwear or sanitary protection
 Minor haemorrhage – blood loss less than 50 ml
that has settled
 Major haemorrhage – blood loss of 50–1000 ml,
with no signs of clinical shock
 Massive haemorrhage – blood loss greater than
1000 ml and/or signs of clinical shock.
 Recurrent APH - > one occasion.
Placenta praevia
 Placenta praevia exists when the placenta is inserted
wholly or in part into the lower segment of the
uterus.
 classified by ultrasound imaging according to what
is relevant clinically:
 if the placenta lies over the internal cervical os -
major praevia;
 if the leading edge of the placenta is in the lower
uterine segment but not covering the cervical os,
minor or partial praevia exists
Risk factors for placenta praevia
 Previous placenta praevia (4-8%)
 Previous caesarean sections (risk increased with no. of CS)
 Previous termination of pregnancy
 Multiparity
 Advanced maternal age (>40 years)
 Multiple pregnancy
 Smoking
 Deficient endometrium due to presence or history of:
• uterine scar
• endometritis
• manual removal of placenta
• curettage
• submucous fibroid
 Assisted conception
Clinical assessment in women presenting with
APH
 First and foremost  Mother and fetal well being
 establish whether urgent intervention is required to
manage maternal or fetal compromise.
 The process of triage includes
 history taking to assess coexisting symptoms such as
pain,
 an assessment of the extent of vaginal bleeding,
 the cardiovascular condition of the mother, and an
assessment of fetal wellbeing
history should be taken.
 pain associated with the haemorrhage.
 Placental abruption - continuous.
 Labour pain- intermittent.
 Risk factors for abruption and placenta praevia should be
identified.
 Reduced fetal movements?
 If the APH is associated with spontaneous or iatrogenic
rupture of the fetal membranes, bleeding from a ruptured
vasa praevia
 Previous cervical smear history -to assess the possibility of
a neoplastic lesion of the cervix
Examination of the woman should be performed
to assess the amount and cause of APH
 General examination- pulse and blood pressure recorded.
 Abdominal palpation
 tenderness or signs of an acute abdomen. The tense or
‘woody’ feel to the uterus on abdominal palpation
indicates a significant abruption.
 Painless bleeding,high presenting part – placenta praevia
 A soft, non-tender uterus may suggest a lower genital
tract cause or bleeding from placenta or vasa praevia.
Speculum examination
 to identify cervical dilatation or visualise a lower
genital tract cause for the APH.
Digital vaginal examination
 If placenta praevia is a possible diagnosis, digital
vaginal examination should not be performed until
an ultrasound has excluded placenta praevia.
Investigation
 FBC
 Coagulation profile
 Bd Gp & Rh and cross match
 USS –location of placenta
 D-dimer
 Colour doppler- TVS –VP
 In all women who are RhD-negative, a Kleihauer test
should be performed to quantify FMH to gauge the dose
of anti-D Ig required
 Fetal monitoring- CTG monitoring
Management
 If preterm delivery is anticipated, a single course of
antenatal corticosteroid (Dexa 12 mg 12hrly 2 doses)
to women between 24 and 34 wk of gestation
 Tocolytics should not be given unless for very
preterm women who need time to transfer to
hospital with NICU
 For very preterm (24 – 26 wk)
 Conservative management – if mother stable
 Delivery of fetus – life threatening
 At these gestations, experienced neonatologists
should be involved
For placenta praevia
 Conservative –MacCafee ‘s regime
 (Premature < 37 wk ,mother haemodynamically
stable , no active bleeding,fetus stable)
 Advise bed rest ,keep pad chart,vital signs
monitoring,USG, Steroids,GSH,daily CTG, and
biophysical profile,Fetal movement count.
 Plan for delivery (>37 wk)
 Crossmatch 4 U of blood
Definitive treatment
 Type I, II (ant)  ARM +/- oxytocin
 If satifactory progress without bleeding  VD
 If bleeding continue  CS
 Type II (post ),III, IV  CS
For Rh negative mother
 Anti-D Ig should be given to all non-sensitised RhD-
negative women after any presentation with APH,
independent of whether routine antenatal prophylactic
anti-D has been administered.
 In the non-sensitised RhD-negative woman in the
event of recurrent vaginal bleeding after 20+0 weeks
of gestation, anti-D Ig should be given at a minimum
of 6-weekly intervals.
 In the non-sensitised RhD-negative woman for all
events after 20+0 weeks of gestation, at least 500 iu
anti-D Ig should be given followed by a test to identify
FMH greater than 4 ml red blood cells; additional anti-
D Ig should be given as required.
Complications of APH
Maternal complications
 Anaemia
 Infection
 Maternal shock
 Renal tubular necrosis
 Consumptive
coagulopathy
 Postpartumhaemorrhage
 Prolonged hospital stay
 Complication of blood
transfusion
Fetal complications
 Fetal hypoxia
 Small for gestational age
and fetal growth
restriction
 Prematurity (iatrogenic
and spontaneous)
 Fetal death
THANK YOU

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Antepartum haemorrhage

  • 1. D R . T H E I N T W A I P H Y O P G 3 , E M Antepartum Haemorrhage
  • 2.  Antepartum haemorrhage (APH) is defined as bleeding from or in to the genital tract, occurring from 24+0 weeks of pregnancy and prior to the birth of the baby.  The most important causes of APH are placenta praevia and placental abruption.  APH complicates 3–5% of pregnancies  leading cause of perinatal and maternal mortality worldwide  Up to one-fifth of very preterm babies are born in association with APH
  • 3. Severity  NO consistent definitions of the severity of APH. It is recognised that the amount of blood lost is often underestimated  The amount of blood coming from the introitus may not represent the total blood lost (for example in a concealed placental abruption).  It is important to assess for signs of clinical shock  The presence of fetal compromise or fetal demise is an important indicator of volume depletion
  • 4. Different terminology used  Spotting – staining, streaking or blood spotting noted on underwear or sanitary protection  Minor haemorrhage – blood loss less than 50 ml that has settled  Major haemorrhage – blood loss of 50–1000 ml, with no signs of clinical shock  Massive haemorrhage – blood loss greater than 1000 ml and/or signs of clinical shock.  Recurrent APH - > one occasion.
  • 5. Placenta praevia  Placenta praevia exists when the placenta is inserted wholly or in part into the lower segment of the uterus.  classified by ultrasound imaging according to what is relevant clinically:  if the placenta lies over the internal cervical os - major praevia;  if the leading edge of the placenta is in the lower uterine segment but not covering the cervical os, minor or partial praevia exists
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  • 8. Risk factors for placenta praevia  Previous placenta praevia (4-8%)  Previous caesarean sections (risk increased with no. of CS)  Previous termination of pregnancy  Multiparity  Advanced maternal age (>40 years)  Multiple pregnancy  Smoking  Deficient endometrium due to presence or history of: • uterine scar • endometritis • manual removal of placenta • curettage • submucous fibroid  Assisted conception
  • 9. Clinical assessment in women presenting with APH  First and foremost  Mother and fetal well being  establish whether urgent intervention is required to manage maternal or fetal compromise.  The process of triage includes  history taking to assess coexisting symptoms such as pain,  an assessment of the extent of vaginal bleeding,  the cardiovascular condition of the mother, and an assessment of fetal wellbeing
  • 10. history should be taken.  pain associated with the haemorrhage.  Placental abruption - continuous.  Labour pain- intermittent.  Risk factors for abruption and placenta praevia should be identified.  Reduced fetal movements?  If the APH is associated with spontaneous or iatrogenic rupture of the fetal membranes, bleeding from a ruptured vasa praevia  Previous cervical smear history -to assess the possibility of a neoplastic lesion of the cervix
  • 11. Examination of the woman should be performed to assess the amount and cause of APH  General examination- pulse and blood pressure recorded.  Abdominal palpation  tenderness or signs of an acute abdomen. The tense or ‘woody’ feel to the uterus on abdominal palpation indicates a significant abruption.  Painless bleeding,high presenting part – placenta praevia  A soft, non-tender uterus may suggest a lower genital tract cause or bleeding from placenta or vasa praevia.
  • 12. Speculum examination  to identify cervical dilatation or visualise a lower genital tract cause for the APH. Digital vaginal examination  If placenta praevia is a possible diagnosis, digital vaginal examination should not be performed until an ultrasound has excluded placenta praevia.
  • 13. Investigation  FBC  Coagulation profile  Bd Gp & Rh and cross match  USS –location of placenta  D-dimer  Colour doppler- TVS –VP  In all women who are RhD-negative, a Kleihauer test should be performed to quantify FMH to gauge the dose of anti-D Ig required  Fetal monitoring- CTG monitoring
  • 14. Management  If preterm delivery is anticipated, a single course of antenatal corticosteroid (Dexa 12 mg 12hrly 2 doses) to women between 24 and 34 wk of gestation  Tocolytics should not be given unless for very preterm women who need time to transfer to hospital with NICU
  • 15.  For very preterm (24 – 26 wk)  Conservative management – if mother stable  Delivery of fetus – life threatening  At these gestations, experienced neonatologists should be involved
  • 16. For placenta praevia  Conservative –MacCafee ‘s regime  (Premature < 37 wk ,mother haemodynamically stable , no active bleeding,fetus stable)  Advise bed rest ,keep pad chart,vital signs monitoring,USG, Steroids,GSH,daily CTG, and biophysical profile,Fetal movement count.  Plan for delivery (>37 wk)  Crossmatch 4 U of blood
  • 17. Definitive treatment  Type I, II (ant)  ARM +/- oxytocin  If satifactory progress without bleeding  VD  If bleeding continue  CS  Type II (post ),III, IV  CS
  • 18. For Rh negative mother  Anti-D Ig should be given to all non-sensitised RhD- negative women after any presentation with APH, independent of whether routine antenatal prophylactic anti-D has been administered.  In the non-sensitised RhD-negative woman in the event of recurrent vaginal bleeding after 20+0 weeks of gestation, anti-D Ig should be given at a minimum of 6-weekly intervals.  In the non-sensitised RhD-negative woman for all events after 20+0 weeks of gestation, at least 500 iu anti-D Ig should be given followed by a test to identify FMH greater than 4 ml red blood cells; additional anti- D Ig should be given as required.
  • 19. Complications of APH Maternal complications  Anaemia  Infection  Maternal shock  Renal tubular necrosis  Consumptive coagulopathy  Postpartumhaemorrhage  Prolonged hospital stay  Complication of blood transfusion Fetal complications  Fetal hypoxia  Small for gestational age and fetal growth restriction  Prematurity (iatrogenic and spontaneous)  Fetal death