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Neoh Hui Pheng Batch 22/A2
ANTEPARTUM HAEMORRHAGE
reference
RCOG GuidelinesObstetrics today
DefinitionAntepartum 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 APHMost of the time unpredictable.
RCOG
SeverityNO 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 episodeRCOG Guidelines
EtiologyPlacenta praeviaAbruptio placentaVasa 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 conceptionRCOG
Clinical classificationMinor :
Type 1 (anterior/posterior) Type 2 anterior
Major: Type 2 posterior (dangerous type)Type 3 Type 4
Deliver vaginallyType 1 Posterior > likelihood of fetal distress
Caesarean sectionType 2 posterior > chance of fetal distressType 3 & 4 anterior –cut 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 VPAntenatal diagnosis –reduced perinatal
mortality and morbidity. Painless vaginal bleeding at the time of
spontaneous rupture of membrane or post amniotomy
Fetal bradycardiaFetal 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 APHMaternal 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 APHFirst 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.
ExaminationSpeculum : -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
InvestigationsFBC Coagulation profileBlood 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
ManagementWHEN 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
ManagementFor 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
Satisfactory progress without bleeding
Vaginal delivery
Bleeding continues
Caesarean section
Caesarean section
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 PlacentaDecide 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
ManagementFor 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