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ANTEPARTUM HAEMORRHAGE

       Neoh Hui Pheng
        Batch 22/A2
reference


 RCOG Guidelines
 Obstetrics today
Definition
 Antepartum haemorrhage (APH) is defined as bleeding
  from or in to the genital tract, occurring from 22 weeks
  (>500g) of pregnancy and prior to the birth of the baby.

 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
 Most of the time unpredictable.



                                                             RCOG
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.
                                                  RCOG Guidelines
Different terminologies 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 episode
                                                     RCOG Guidelines
Etiology
 Placenta praevia
 Abruptio placenta
 Vasa praevia
 Excessive show
 Local causes ( bleeding from cervix, vagina and
 vulva )

 Inderterminate APH
Placenta Praevia (PP)
 Implantation of placenta over or near the internal
  os of cervix.
 Confirm diagnosis of PP can be done at 28 weeks
  when LUS forming.

Leading cause of vaginal bleeding in the 2nd and 3rd
 trimester.
Classification
Risk Factors of Placenta Praevia
 Previous placenta praevia (4-8%)
 Previous caesarean sections ( risk with      numbers of c-section)
 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
                                                                       RCOG
Clinical classification
 Minor :                                Deliver vaginally
                                         Type 1 Posterior > likelihood of
    Type 1 (anterior/posterior)         fetal distress
    Type 2 anterior



 Major:                                    Caesarean section
    Type 2 posterior (dangerous type)      Type 2 posterior >
    Type 3                                 chance of fetal distress
                                            Type 3 & 4 anterior –cut
    Type 4                                 through placenta to
                                            deliver. Hence need to be
                                            fast and efficient.
Abruptio Placenta (AP)
 Separation of normally located placenta after 22
 weeks of gestation ( > 500g) and prior to delivery
 of fetus.
Risk factors:
- Previous history of AP
- Maternal hypertension
- Advanced maternal age
- Trauma ( domestic violence, accident, fall)
- Smoking/alcohol/cocaine
- Short umbilical cord
- Sudden decompression of uterus (
  PROM/delivery of 1st twins)
- Retroplacental fibroids
- Idiopathic
Obstetrics Emergency!!
Diagnosed CLINICALLY :
 Painful vaginal bleeding -80%
 Tense and tender abdomen/back pain (70%)
 Fetal distress( 60%)
 Abnormal uterine contractions (hypertonic and high
  frequency)
 Preterm labour ( 25%)
 Fetal death ( 15%)

Ultrasound is NOT USEFUL to diagnose AP.
  Retroplacental clots (hyperechoic) easily missed.
                                              Obstetrics today
Vasa Praevia (VP)
 Rupture of fetal vessels that run in membrane
 below fetal presenting part which is unsupported
 by placenta/ umbilical cord.

 Predisposing Factors:
-Velamentous insertion of the umbilical cord
-Accesory placental lobes
-Multiple gestations

                                          Obstetrics today
The term velamentous
insertion is used to
describe the condition in
which the umbilical cord
inserts on the
chorioamniotic
membranes rather than on
the placental mass.
Diagnosis of VP
 Antenatal diagnosis –reduced perinatal mortality and
    morbidity.
   Painless vaginal bleeding at the time of spontaneous
    rupture of membrane or post amniotomy
   Fetal bradycardia
   Fetal shock or death can occur rapidly at the time of
    diagnosis due to blood loss constitutes a major bulk of
    blood volume is fetus ( 3kg fetus-300ml)
   Hence, ALWAYS check the fetal heart after rupture of
    membrane or amniotomy.
   Definitive diagnosis by inspecting the placenta and
    fetal membrane after delivery.
                                                 Obstetrics today
Complications of APH
Maternal complications               Fetal complications
Anaemia                              Fetal hypoxia
Infection                            Small for gestational age and fetal
                                     growth restriction
Maternal shock                       Prematurity (iatrogenic and
                                     spontaneous)
Renal tubular necrosis               Fetal death
Consumptive coagulopathy
Postpartum haemorrhage
Prolonged hospital stay
Psychological sequelae
Complications of blood transfusion

                                                            RCOG Guidelines
Clinical assessment in APH
 First and foremost Mother and fetal well
 being (mother is the priority)

 establish whether urgent intervention is required
 to manage maternal or fetal compromise.

 Assess the extent of vaginal bleeding,
 cardiovascular condition of the mother

 Assess fetal wellbeing.
Full History
Should be taken after the mother is stable.
 associated pain with the haemorrhage?
Continuous pain : Placental abruption.
Intermittent pain : Labour.
 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 : ruptured
  vasa praevia
 Previous cervical smear history possibility of Ca
  cervix. Symptomatic pregnant women usually present
  with APH (mostly postcoital) or vaginal discharge.
Examination
 General: PULSE & BP ( a MUST!)
 Abdomen:
- The tense, tender or ‘woody’ feel to the uterus
  indicates a significant abruption.
- Painless bleeding, high fetal presenting part –
  Placenta praevia
- soft, non-tender uterus may suggest a lower
  genital tract cause or bleeding from placenta or
  vasa praevia.
Examination
 Speculum :
-identify cervical dilatation or visualise a lower
  genital tract cause.

 Digital vaginal examination
- Should NOT be done until Placenta Praevia has
  been excluded by USG.

                                              RCOG Guidelines
Investigations
 FBC
 Coagulation profile
 Blood Grouping and CXM, GSH.
 Ultrasound- TRO PP/ IUD
 D-dimer : AP
  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
                                            RCOG Guidelines
Management
 WHEN to admit?
 Based on individual assessment
-Discharge after reassurance and counselling
Women presenting with spotting who are no longer
  bleeding and where placenta praevia has been
  Excluded.
However, a woman with spotting + previous IUD due to
  placenta abruption, an admission would be
  appropriate.

- All women with APH heavier than spotting and women
   with ongoing bleeding should remain in hospital at
   least until the bleeding has stopped.
Management
 If preterm delivery is anticipated, a single course of
  antenatal corticosteroids ( dexamethasone 12mg 12 hourly
  ,2 doses) to women between 24 and 34 weeks 6 days 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 weeks) ,
-conservative management if mother is stable .
-Delivery of fetus – life threatening
   At these gestations, experienced neonatologists should be
  involved in the counselling of the woman and her partner
                                                           RCOG
Management
For Placenta Praevia
 Conservative – MaCafee’s regime
( premature < 37 weeks;mother haemodynamically
  stable,no active bleeding, fetus stable)
-advise bed rest, keep pad chart, vital signs
  monitoring , Ultrasound, steroids, GSH, Daily
  CTG and biophysical profile, fetal movement
  count.

 Plan for delivery ( >37 weeks)
Crossmatch 4 units of blood.
Definitive treatment

      Type I,II(ant)                         Type II( post), III,IV



  ARM +/- oxytocin
                                             Caesarean section



Satisfactory progress
without bleeding        Bleeding continues



                        Caesarean section
Vaginal delivery
For Abruptio placenta,(obs
emergency)
 ICU admission : Close monitoring and
    resuscitation!
-   ABC ( high flow O2, aggressive fluid
    resuscitation)
-   Continuous Vital signs monitoring and urine
    output
-   Monitor vaginal bleeding – strict pad chart
-   Continuous CTG for fetal heart rate
-   Crossmatch 4 units of blood
-   FFP – coagulopathy
-   Dexamethasone – preterm
Abruptio Placenta
Decide Mode of delivery
 Vaginal delivery – when fetal death
 Caesarean section –if maternal/ fetal health
  compromised
- Indicated when early DIC sets in
- Consent should be taken for hysterectomy in
  case bleeding could not be controlled.

                                          Obstetrics today
Management
 For Rh negative mothers,
Anti-D Ig should be given to all after any presentation
 with APH, independent of whether routine antenatal
 prophylactic anti-D has been administered.

In the non-sensitised RhD-negative woman for all
  events after 20 weeks of gestation, at least 500 iu
anti-D Ig should be given followed by a test to identify
  FMH, if greater than 4 ml red blood cells; additional
anti-D Ig should be given as required.
                                                 RCOG Guidelines
Antepartum haemorrhage

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Antepartum haemorrhage

  • 1. ANTEPARTUM HAEMORRHAGE Neoh Hui Pheng Batch 22/A2
  • 3. Definition  Antepartum haemorrhage (APH) is defined as bleeding from or in to the genital tract, occurring from 22 weeks (>500g) of pregnancy and prior to the birth of the baby.  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  Most of the time unpredictable. RCOG
  • 4. 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. RCOG Guidelines
  • 5. Different terminologies 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 episode RCOG Guidelines
  • 6. Etiology  Placenta praevia  Abruptio placenta  Vasa praevia  Excessive show  Local causes ( bleeding from cervix, vagina and vulva )  Inderterminate APH
  • 7. Placenta Praevia (PP)  Implantation of placenta over or near the internal os of cervix.  Confirm diagnosis of PP can be done at 28 weeks when LUS forming. Leading cause of vaginal bleeding in the 2nd and 3rd trimester.
  • 9. Risk Factors of Placenta Praevia  Previous placenta praevia (4-8%)  Previous caesarean sections ( risk with numbers of c-section)  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 RCOG
  • 10. Clinical classification  Minor : Deliver vaginally Type 1 Posterior > likelihood of  Type 1 (anterior/posterior) fetal distress  Type 2 anterior  Major: Caesarean section  Type 2 posterior (dangerous type) Type 2 posterior >  Type 3 chance of fetal distress Type 3 & 4 anterior –cut  Type 4 through placenta to deliver. Hence need to be fast and efficient.
  • 11. Abruptio Placenta (AP)  Separation of normally located placenta after 22 weeks of gestation ( > 500g) and prior to delivery of fetus.
  • 12. Risk factors: - Previous history of AP - Maternal hypertension - Advanced maternal age - Trauma ( domestic violence, accident, fall) - Smoking/alcohol/cocaine - Short umbilical cord - Sudden decompression of uterus ( PROM/delivery of 1st twins) - Retroplacental fibroids - Idiopathic
  • 13. Obstetrics Emergency!! Diagnosed CLINICALLY :  Painful vaginal bleeding -80%  Tense and tender abdomen/back pain (70%)  Fetal distress( 60%)  Abnormal uterine contractions (hypertonic and high frequency)  Preterm labour ( 25%)  Fetal death ( 15%) Ultrasound is NOT USEFUL to diagnose AP. Retroplacental clots (hyperechoic) easily missed. Obstetrics today
  • 14. Vasa Praevia (VP)  Rupture of fetal vessels that run in membrane below fetal presenting part which is unsupported by placenta/ umbilical cord.  Predisposing Factors: -Velamentous insertion of the umbilical cord -Accesory placental lobes -Multiple gestations Obstetrics today
  • 15. The term velamentous insertion is used to describe the condition in which the umbilical cord inserts on the chorioamniotic membranes rather than on the placental mass.
  • 16.
  • 17. Diagnosis of VP  Antenatal diagnosis –reduced perinatal mortality and morbidity.  Painless vaginal bleeding at the time of spontaneous rupture of membrane or post amniotomy  Fetal bradycardia  Fetal shock or death can occur rapidly at the time of diagnosis due to blood loss constitutes a major bulk of blood volume is fetus ( 3kg fetus-300ml)  Hence, ALWAYS check the fetal heart after rupture of membrane or amniotomy.  Definitive diagnosis by inspecting the placenta and fetal membrane after delivery. Obstetrics today
  • 18. Complications of APH Maternal complications Fetal complications Anaemia Fetal hypoxia Infection Small for gestational age and fetal growth restriction Maternal shock Prematurity (iatrogenic and spontaneous) Renal tubular necrosis Fetal death Consumptive coagulopathy Postpartum haemorrhage Prolonged hospital stay Psychological sequelae Complications of blood transfusion RCOG Guidelines
  • 19. Clinical assessment in APH  First and foremost Mother and fetal well being (mother is the priority)  establish whether urgent intervention is required to manage maternal or fetal compromise.  Assess the extent of vaginal bleeding, cardiovascular condition of the mother  Assess fetal wellbeing.
  • 20. Full History Should be taken after the mother is stable.  associated pain with the haemorrhage? Continuous pain : Placental abruption. Intermittent pain : Labour.  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 : ruptured vasa praevia  Previous cervical smear history possibility of Ca cervix. Symptomatic pregnant women usually present with APH (mostly postcoital) or vaginal discharge.
  • 21. Examination  General: PULSE & BP ( a MUST!)  Abdomen: - The tense, tender or ‘woody’ feel to the uterus indicates a significant abruption. - Painless bleeding, high fetal presenting part – Placenta praevia - soft, non-tender uterus may suggest a lower genital tract cause or bleeding from placenta or vasa praevia.
  • 22. Examination  Speculum : -identify cervical dilatation or visualise a lower genital tract cause.  Digital vaginal examination - Should NOT be done until Placenta Praevia has been excluded by USG. RCOG Guidelines
  • 23. Investigations  FBC  Coagulation profile  Blood Grouping and CXM, GSH.  Ultrasound- TRO PP/ IUD  D-dimer : AP  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 RCOG Guidelines
  • 24. Management  WHEN to admit?  Based on individual assessment -Discharge after reassurance and counselling Women presenting with spotting who are no longer bleeding and where placenta praevia has been Excluded. However, a woman with spotting + previous IUD due to placenta abruption, an admission would be appropriate. - All women with APH heavier than spotting and women with ongoing bleeding should remain in hospital at least until the bleeding has stopped.
  • 25. Management  If preterm delivery is anticipated, a single course of antenatal corticosteroids ( dexamethasone 12mg 12 hourly ,2 doses) to women between 24 and 34 weeks 6 days 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 weeks) , -conservative management if mother is stable . -Delivery of fetus – life threatening At these gestations, experienced neonatologists should be involved in the counselling of the woman and her partner RCOG
  • 26. Management For Placenta Praevia  Conservative – MaCafee’s regime ( premature < 37 weeks;mother haemodynamically stable,no active bleeding, fetus stable) -advise bed rest, keep pad chart, vital signs monitoring , Ultrasound, steroids, GSH, Daily CTG and biophysical profile, fetal movement count.  Plan for delivery ( >37 weeks) Crossmatch 4 units of blood.
  • 27. Definitive treatment Type I,II(ant) Type II( post), III,IV ARM +/- oxytocin Caesarean section Satisfactory progress without bleeding Bleeding continues Caesarean section Vaginal delivery
  • 28. For Abruptio placenta,(obs emergency)  ICU admission : Close monitoring and resuscitation! - ABC ( high flow O2, aggressive fluid resuscitation) - Continuous Vital signs monitoring and urine output - Monitor vaginal bleeding – strict pad chart - Continuous CTG for fetal heart rate - Crossmatch 4 units of blood - FFP – coagulopathy - Dexamethasone – preterm
  • 29. Abruptio Placenta Decide Mode of delivery  Vaginal delivery – when fetal death  Caesarean section –if maternal/ fetal health compromised - Indicated when early DIC sets in - Consent should be taken for hysterectomy in case bleeding could not be controlled. Obstetrics today
  • 30. Management  For Rh negative mothers, Anti-D Ig should be given to all after any presentation with APH, independent of whether routine antenatal prophylactic anti-D has been administered. In the non-sensitised RhD-negative woman for all events after 20 weeks of gestation, at least 500 iu anti-D Ig should be given followed by a test to identify FMH, if greater than 4 ml red blood cells; additional anti-D Ig should be given as required. RCOG Guidelines