Antepartum Haemorrhage
This guideline provides recommendations for managing antepartum haemorrhage (APH), defined as bleeding from the genital tract from 24 weeks of pregnancy until birth. APH complicates 3-5% of pregnancies and is a leading cause of perinatal and maternal mortality.
Structured like the source document: use the contents list to jump to each section, then revise the main bullet points and sub-points.
Contents
Jump to any section from the PDF-style summary.
- 1Introduction and DefinitionsAntepartum haemorrhage (APH) is defined as bleeding from or into the genital tract from 24+0 weeks of pregnancy until birth. It complicates 3–5% of pregnancies and is a leading cause of maternal and perinatal mortality, with placenta praevia and placental abruption being the most important causes.
- 2Risk Factors, Prediction and PreventionAPH is generally unpredictable, with most cases occurring in low-risk women. Prevention focuses on modifying risk factors, as other interventions have limited evidence. Risk factors differ for placental abruption and placenta praevia.
- 3Complications and OutcomesAPH is associated with significant maternal and perinatal morbidity and mortality. Complications are more likely with placental causes, heavy bleeding, and early gestations. Unexplained APH also carries increased risks.
- 4Initial Assessment and ManagementWomen with APH require immediate assessment in a hospital with full obstetric, anaesthetic, neonatal, and transfusion facilities. The primary goal is to rapidly identify and manage maternal or fetal compromise, prioritising maternal stabilisation.
- 5InvestigationsInvestigations aim to assess the physiological consequences of the APH and determine the cause. Placental abruption remains a clinical diagnosis, as no test is reliably diagnostic.
- 6Inpatient and Antenatal ManagementManagement following an APH episode involves decisions on hospitalisation, use of corticosteroids and tocolytics, and modification of subsequent antenatal care.
- 7Labour and DeliveryDecisions regarding the timing and mode of delivery depend on maternal and fetal condition, gestational age, and the cause of APH. Active management of the third stage is crucial due to the high risk of PPH.
- 8Specific Management ScenariosThis section covers key management points for RhD-negative women, massive APH, coagulopathy, and women on anticoagulant therapy.
- 9Neonatal, Postnatal and TrainingCare extends beyond the APH event to include specialised neonatal management, comprehensive postnatal support, and regular multidisciplinary team training to maintain skills.
Introduction and Definitions
Antepartum haemorrhage (APH) is defined as bleeding from or into the genital tract from 24+0 weeks of pregnancy until birth. It complicates 3–5% of pregnancies and is a leading cause of maternal and perinatal mortality, with placenta praevia and placental abruption being the most important causes.
APH complicates 3–5% of pregnancies. Up to one-fifth of very preterm babies are born in association with APH.
The main causes are placenta praevia and placental abruption. Other causes include local lesions of the vulva, vagina, or cervix. If no cause is identified, it is termed 'unexplained APH'.
The amount of blood lost is often underestimated. Clinical assessment must include signs of shock, as visible loss may not represent total loss (e.g., concealed abruption). Fetal compromise or demise is an important indicator of significant volume depletion.
Recurrent APH is defined as episodes of APH occurring on more than one occasion.
Definitions of APH Severity
| Classification | Definition |
|---|---|
| Spotting | Staining, streaking, or blood spotting on underwear or sanitary protection. |
| Minor haemorrhage | Blood loss < 50 ml that has settled. |
| Major haemorrhage | Blood loss of 50–1000 ml, with no signs of clinical shock. |
| Massive haemorrhage | Blood loss > 1000 ml and/or signs of clinical shock. |
Risk Factors, Prediction and Prevention
APH is generally unpredictable, with most cases occurring in low-risk women. Prevention focuses on modifying risk factors, as other interventions have limited evidence. Risk factors differ for placental abruption and placenta praevia.
- C
APH has a heterogeneous pathophysiology and cannot be reliably predicted. Approximately 70% of placental abruption cases occur in low-risk pregnancies.
- P
Women should be advised, encouraged and helped to change modifiable risk factors such as smoking and drug misuse (cocaine, amphetamines).
Risk Factors for Placental Abruption:
The most predictive risk factor is abruption in a previous pregnancy (recurrence rate 4.4% after one, 19–25% after two).
Other risk factors include: pre-eclampsia, fetal growth restriction, non-vertex presentation, polyhydramnios, advanced maternal age, multiparity, low BMI, assisted reproductive techniques, intrauterine infection, PPROM, abdominal trauma, and first-trimester bleeding (especially with an intrauterine haematoma).
Maternal thrombophilias (e.g., Factor V Leiden, Prothrombin 20210A) are associated with an increased risk, though the association may be weak.
Prevention of Placental Abruption:
Evidence for folic acid supplementation is conflicting.
There are no good data to support antithrombotic therapy (aspirin +/- LMWH) to prevent abruption, even in women with thrombophilia.
Prevention of Haemorrhage from Placenta Praevia:
- P
It is good practice to avoid vaginal and rectal examinations and advise women to avoid penetrative sexual intercourse.
Cervical cerclage is not recommended to prevent bleeding or prolong pregnancy outside of a clinical trial.
There is no role for prophylactic tocolytics to prevent bleeding.
Risk Factors for Placenta Praevia
| Risk Factor | Associated Risk/Odds |
|---|---|
| Previous placenta praevia | Adjusted OR 9.7 |
| Previous caesarean sections (overall) | RR 2.6 |
| One previous caesarean section | OR 2.2 |
| Two previous caesarean sections | OR 4.1 |
| Three+ previous caesarean sections | OR 22.4 |
| Previous termination of pregnancy | |
| Multiparity | |
| Advanced maternal age (>40 years) | |
| Multiple pregnancy | |
| Smoking | |
| Assisted conception | |
| Deficient endometrium (e.g., uterine scar, curettage) |
Complications and Outcomes
APH is associated with significant maternal and perinatal morbidity and mortality. Complications are more likely with placental causes, heavy bleeding, and early gestations. Unexplained APH also carries increased risks.
- P
Clinicians should be aware of the potential for significant maternal and perinatal morbidity and mortality.
- P
Health professionals should be aware that domestic violence in pregnancy may result in APH and ask about it in cases of repeated presentations.
Unexplained APH is associated with increased risk of adverse outcomes:
Increased frequency of preterm delivery (OR 3.17), stillbirth (OR 2.09), and fetal anomalies (OR 1.42).
Babies are more likely to be small for gestational age, admitted to NICU, and develop hyperbilirubinaemia.
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 (DIC) | |
| Postpartum haemorrhage | |
| Prolonged hospital stay & psychological sequelae | |
| Complications of blood transfusion |
Initial Assessment and Management
Women with APH require immediate assessment in a hospital with full obstetric, anaesthetic, neonatal, and transfusion facilities. The primary goal is to rapidly identify and manage maternal or fetal compromise, prioritising maternal stabilisation.
- P
Women with APH should be managed in a hospital with facilities for resuscitation, blood transfusion, and emergency operative delivery, supported by a multidisciplinary team.
- P
The first step is to establish if urgent intervention is required for maternal or fetal compromise.
In major or massive haemorrhage, immediately begin resuscitation (Airway, Breathing, Circulation). The mother is the priority and should be stabilised before establishing the fetal condition.
If there is no compromise, take a full history: assess for pain (continuous suggests abruption, intermittent suggests labour), risk factors, fetal movements, and ruptured membranes (consider vasa praevia).
Perform an examination:
Abdominal palpation: A tense or 'woody' uterus suggests significant abruption. A soft, non-tender uterus may suggest placenta praevia or a lower genital tract cause.
Speculum examination: Can identify cervical dilatation or a local cause. Refer for colposcopy if the cervix appears suspicious.
A digital vaginal examination should NOT be performed if placenta praevia is a possible diagnosis until it has been excluded by ultrasound.
Investigations
Investigations aim to assess the physiological consequences of the APH and determine the cause. Placental abruption remains a clinical diagnosis, as no test is reliably diagnostic.
- D
Placental abruption is a clinical diagnosis; there are no sensitive or reliable diagnostic tests available.
- C
Ultrasound can be used to diagnose placenta praevia but does not exclude abruption. It has poor sensitivity (24%) for detecting retroplacental clot, but high specificity (96%).
- D
Perform a Kleihauer test in rhesus D (RhD)-negative women to quantify fetomaternal haemorrhage (FMH) and determine the required dose of anti-D immunoglobulin. It is not a sensitive test for diagnosing abruption.
- P
Assess the fetal heart rate with a cardiotocograph (CTG) once the mother is stable or resuscitation has commenced. An abnormal CTG in abruption is associated with poor fetal outcome and delivery should be expedited.
- D
If fetal viability cannot be detected by external auscultation, an ultrasound should be used to establish fetal heart pulsation.
Continuous FHR monitoring is not advised at gestations <26+0 weeks if active obstetric intervention for the fetus is not planned.
Maternal Blood Tests in APH
| Severity of Haemorrhage | Investigations |
|---|---|
| Major or Massive | Full blood count, Coagulation screen, U&Es, LFTs, and cross-match 4 units of blood. |
| Minor | Full blood count and Group & Save. A coagulation screen is not indicated unless the platelet count is abnormal. |
Inpatient and Antenatal Management
Management following an APH episode involves decisions on hospitalisation, use of corticosteroids and tocolytics, and modification of subsequent antenatal care.
Hospitalisation:
- P
Women with spotting that has resolved, where placenta praevia is excluded, can go home after a reassuring assessment.
- P
Women with APH heavier than spotting or with ongoing bleeding should remain in hospital at least until the bleeding has stopped.
Antenatal Corticosteroids:
- A
Offer a single course of antenatal corticosteroids to women between 24+0 and 34+6 weeks of gestation at risk of preterm birth due to APH.
- P
In women with minor, resolved spotting from a likely non-placental cause, corticosteroids are unlikely to be of benefit but can be considered.
Tocolytic Therapy:
- P
Tocolysis should NOT be used in a woman with a major APH, who is haemodynamically unstable, or if there is fetal compromise. It is contraindicated in placental abruption.
- P
A senior obstetrician should make any decision to initiate tocolysis. It may be considered for very preterm women needing transfer or to complete a course of corticosteroids, provided they are stable.
Altering Antenatal Care Following APH:
- P
Following APH from a cervical ectropion, subsequent care need not be altered.
- D
Following APH from placental abruption or unexplained APH, reclassify the pregnancy as ‘high risk’. Care should be consultant-led with serial ultrasound scans for fetal growth.
Labour and Delivery
Decisions regarding the timing and mode of delivery depend on maternal and fetal condition, gestational age, and the cause of APH. Active management of the third stage is crucial due to the high risk of PPH.
Timing and Mode of Delivery:
- P
Women with APH and associated maternal and/or fetal compromise require immediate delivery.
- P
If the fetus is compromised, caesarean section is the appropriate method, with concurrent maternal resuscitation.
- P
If fetal death is diagnosed, vaginal birth is recommended for most women, provided the mother is stable.
For APH after 37+0 weeks that has settled, consider induction of labour to avoid risks of abruption.
For APH before 37+0 weeks with no compromise and settled bleeding, there is no evidence to support elective premature delivery.
Intrapartum Fetal Monitoring:
- D
Women in labour with active vaginal bleeding require continuous electronic fetal monitoring (EFM).
- D
Recommend continuous EFM for women in preterm labour whose pregnancy was complicated by major APH, recurrent minor APH, or suspected abruption.
- P
Intermittent auscultation is appropriate for women who have had one episode of minor APH with no subsequent concerns.
Anaesthesia:
- P
Regional anaesthesia is recommended for operative delivery unless contraindicated (e.g., maternal cardiovascular instability, coagulopathy).
- P
Consider a general anaesthetic for caesarean section in cases of maternal or fetal compromise to facilitate resuscitation and expedite delivery.
Management of the Third Stage of Labour:
- P
Postpartum haemorrhage (PPH) should be anticipated in women who have experienced APH.
- A
Women with APH from placental abruption or placenta praevia should be strongly recommended to receive active management of the third stage of labour.
- B
Consider using ergometrine-oxytocin (Syntometrine®) for the third stage in these women, in the absence of hypertension.
Specific Management Scenarios
This section covers key management points for RhD-negative women, massive APH, coagulopathy, and women on anticoagulant therapy.
Anti-D Immunoglobulin for RhD-Negative Women:
- B
Anti-D Ig should be given to all non-sensitised RhD-negative women after any presentation with APH, regardless of whether routine prophylaxis has been given.
- D
For bleeding after 20+0 weeks, give at least 500 iu of anti-D Ig and perform a test to quantify FMH, giving more anti-D if required.
- D
In recurrent bleeding, anti-D Ig should be given at a minimum of 6-weekly intervals.
Management of Massive APH (>1000ml or shock):
- P
Management should follow locally devised multidisciplinary protocols for massive obstetric haemorrhage.
- P
The core team should include a consultant obstetrician, anaesthetist, haematologist, and the midwifery labour ward coordinator.
The four pillars of management are: Communication, Resuscitation, Monitoring/Investigation, and Arresting the bleeding (definitive treatment is delivery of fetus and placenta).
Blood Products and Coagulopathy:
- D
Consider Disseminated Intravascular Coagulation (DIC) in women with massive blood loss or a major placental abruption.
If DIC is suspected, urgently request clotting studies, platelet count, and seek advice from a haematologist.
Empirically give up to 4 units of FFP and 10 units of cryoprecipitate (two packs) while awaiting results in cases of relentless bleeding.
APH with Anticoagulant Therapy:
- D
Advise women on anticoagulants to stop their medication and attend hospital urgently if any vaginal bleeding occurs.
For women at high risk of haemorrhage where continued heparin is essential, manage with intravenous unfractionated heparin until risk factors resolve.
Therapeutic Goals in Massive Blood Loss Management
| Parameter | Target |
|---|---|
| Haemoglobin | > 8 g/dl |
| Platelet count | > 75 x 10⁹/l |
| Prothrombin time (PT) | < 1.5 x mean control |
| Activated partial thromboplastin time (aPTT) | < 1.5 x mean control |
| Fibrinogen | > 1.0 g/l |
Neonatal, Postnatal and Training
Care extends beyond the APH event to include specialised neonatal management, comprehensive postnatal support, and regular multidisciplinary team training to maintain skills.
Neonatal Management:
- P
In major or massive APH, the neonate should be assessed by a senior paediatrician/neonatologist due to the risk of fetal anaemia and compromise.
In abruption and vasa praevia, an experienced paediatrician/neonatologist should be present at delivery to manage potential neonatal anaemia.
An experienced paediatrician/neonatologist should attend delivery if an anterior placenta praevia is incised during caesarean section.
Management in Extreme Preterm Pregnancy (24+0 to 26+0 weeks):
- P
The mother’s life always takes priority; she must be resuscitated and stabilised before any decision regarding delivery.
- D
A senior paediatrician/neonatologist should be involved in counselling women when extreme preterm birth is likely.
Conservative management is usually appropriate if the mother's condition is stable.
Postnatal Issues:
- P
Postnatal management after major or massive APH should include thromboprophylaxis, debriefing, and clinical incident reporting.
An experienced obstetrician should debrief the woman and her partner, offering a follow-up appointment and support contacts.
Commence or reinstitute thromboprophylaxis as soon as the immediate risk of haemorrhage is reduced, as haemorrhage and transfusion are VTE risk factors.
Obstetric Skill Drills:
- C
Management of a major APH should be included in obstetric skill drills.
Practical, multi-professional training in obstetric emergencies increases knowledge and promotes effective teamworking.