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Antepartum haemorrhage

Medical Professionals

Professional Reference articles are designed for health professionals to use. They are written by UK doctors and based on research evidence, UK and European Guidelines. You may find one of our health articles more useful.

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What is an antepartum haemorrhage?

Antepartum haemorrhage (APH) is usually defined as bleeding from the birth canal after the 24th week of pregnancy1 . It can occur at any time until the second stage of labour is complete; bleeding following the birth of the baby is postpartum haemorrhage.

Bleeding before 24 completed weeks of pregnancy is miscarriage, which is discussed in the separate Miscarriage article.


In the UK and Ireland there were 14 women who died from obstetric haemorrhage during or up to six weeks after the end of pregnancy in 2016-18. This represents an overall mortality rate of 0.63 per 100,000 maternities (95% CI 0.32-0.97)2 . There were six deaths due to antepartum haemorrhage: three followed placental abruption and three were after placenta praevia percreta. Worldwide, obstetric haemorrhage is responsible for 27% of all maternal deaths, most of which occur in low- and middle-income countries3 .

  • It affects 3-5% of all pregnancies1 .

  • Up to 20% of very preterm babies are born in association with APH, which explains the association between APH and cerebral palsy.

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Antepartum haemorrhage causes (aetiology)1

No definite cause is diagnosed in about 50% of all women who present with antepartum haemorrhage; however, placenta praevia and placental abruption are the major identifiable causes:

  • Placenta praevia: insertion of the placenta, partially or fully, in the lower segment of the uterus. See the separate Placenta Praevia article. A 2017 study found a total of 29 articles were included. The pooled overall prevalence of APH among pregnant women with placenta previa was 51.6%

  • Placental abruption: premature separation of a normally placed placenta. See the separate Placenta Problems (Placenta Accreta and Placental Abruption) article.

  • Local causes - eg, vulval or cervical infection, trauma or tumours.

  • Partner violence is common in pregnancy, occurring in 2.8% of pregnant women in a Canadian population-based study4 . It may result in APH. Women should be asked about this, particularly if there are repeated episodes. See the separate Domestic Violence article.

  • Vasa praevia: bleeding from fetal vessels in the fetal membranes, leading to high risk of fetal haemorrhage and death at rupture of the membranes. See the separate Placenta Problems (Placenta Accreta and Placental Abruption) article

  • Uterine rupture: rare but very dangerous for both mother and baby. See the separate Uterine Rupture article

  • Inherited bleeding problems are very rare, occurring in 1 in 10,000 women5 .

  • Whilst risk factors for APH, in particular for placenta praevia and placental abruption, have been identified, APH cannot be predicted; 70% of cases of placental abruption occur in low-risk pregnancies.

  • There is limited evidence that APH can be prevented but women should be encouraged to change modifiable risk factors such as smoking and cocaine and amfetamine abuse.

  • Antenatal anaemia should be investigated and treated. Iron-deficiency anaemia not only reduces a woman's tolerance to bleeding but may also contribute to uterine atony2 .

Antepartum haemorrhage symptoms

  • Bleeding, which may be accompanied by pain (suggestive of abruption) or be painless (suggesting praevia).

  • Uterine contractions may be provoked.

  • There may be malpresentation or failure of the fetal head to engage, with placenta praevia.

  • There may be associated signs of fetal distress.

  • If the bleeding is severe, the mother may show signs of hypovolaemic shock; however, young, fit, pregnant women can compensate very well until sudden and catastrophic decompensation occurs2 .

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Antepartum haemorrhage treatment and management1

Always admit the patient to hospital for assessment and management, even if bleeding is only a very small amount; there may be a large amount of concealed bleeding with only a small amount of revealed vaginal bleeding. Phone 999/112/911 if there are any major concerns regarding maternal or fetal well-being.

  • Estimate amount of blood loss. This is often underestimated and needs to combined with an assessment of signs of clinical shock:

    • Minor haemorrhage = blood loss <50 ml and has stopped.

    • Major haemorrhage = blood loss 50-1000 ml with no signs of shock.

    • Massive haemorrhage = blood loss >1000 ml and/or signs of shock.

  • The mainstays of management of massive haemorrhage are effective communication between clinical staff, resuscitation, monitoring and accurate diagnosis of the underlying cause. The bleeding will be arrested by delivery of the fetus.

  • Severe bleeding: the mother's life should take priority. Any decision regarding the delivery of the baby should wait until the mother's condition is stable.

  • Fetal distress: urgent delivery of the baby, irrespective of gestational age. Fetal compromise is an important indicator of reduced circulating blood volume.

  • No vaginal examination should be attempted, at least until a placenta praevia is excluded by ultrasound. It may initiate torrential bleeding from a placenta praevia.

  • Resuscitation can be inadequate because of underestimation of blood loss and misleading maternal response, especially in small women. For example, a woman who weighs 55 kg will have lost almost 30% of her blood volume if she loses 1500 ml of blood, whereas for a woman of 70 kg, this represents about 20% of her blood volume2 .

  • Blood tests:

    • FBC and 'group and save'. NB: initial Hb may not reflect degree of blood loss. Low platelet count may suggest significant abruption.

    • Clotting studies, if platelet count is abnormal, as coagulopathy is common and should be anticipated.

    • Crossmatch four units and check U&Es and LFTs, if there is major or massive haemorrhage.

  • Gentle palpation of the abdomen to determine the gestational age of the fetus, presentation and position.

  • Fetal monitoring.

  • Arrange urgent ultrasound to exclude placenta praevia; ultrasound cannot exclude placental abruption, which is a clinical diagnosis.

  • With every episode of bleeding, a rhesus-negative woman should have a Kleihauer test and be given prophylactic anti-D immunoglobulin6 .

  • Maternal corticosteroids should be offered to any woman at risk of preterm birth, who is between 24+0 and 33+6 weeks of gestation7 .

Further management

  • Further management will depend on fetal distress, the cause of the APH, the extent of bleeding and gestation.

  • All women need to be assessed individually, taking into account not only the amount of blood loss but also any relevant current or past medical and obstetric history.

  • Placenta praevia: see the separate Placenta Praevia article.

  • Moderate or severe placental abruption: see the separate Placenta Problems (Placenta Accreta and Placental Abruption) article.



  • Maternal mortality is lower if managed by an experienced obstetrician and if no vaginal examination is performed before admission to hospital.

  • According to a 2017 systematic review of 123 studies abruption is the most frequently reported risk factor for stillbirth (range: 3.4-51.8%), neonatal death (range: 1.1-19%), and overall perinatal mortality (range: 4-56.3%)8 . However, more than half (55%) of excess perinatal deaths associated with abruption are attributed to preterm birth.

  • In pregnancies when the cause of APH is not known, there is still a greater risk of preterm delivery and induced labour but no increase in perinatal mortality after adjusting for gestational age9 .

Further reading and references

  1. Antepartum Haemorrhage; Royal College of Obstetricians and Gynaecologists (December 2011)
  2. Saving Lives, Improving Mothers’ Care; Lessons learned to inform maternity care from the UK and Ireland Confidential Enquiries into Maternal Deaths and Morbidity 2016-18, December 2020
  3. Say L, Chou D, Gemmill A, et al; Global causes of maternal death: a WHO systematic analysis. Lancet Glob Health. 2014 Jun;2(6):e323-33. doi: 10.1016/S2214-109X(14)70227-X. Epub 2014 May 5.
  4. Daoud N, Urquia ML, O'Campo P, et al; Prevalence of abuse and violence before, during, and after pregnancy in a national sample of Canadian women. Am J Public Health. 2012 Oct;102(10):1893-901. Epub 2012 Aug 16.
  5. Kadir RA, Aledort LM; Obstetrical and gynaecological bleeding: a common presenting symptom. Clin Lab Haematol. 2000 Oct;22 Suppl 1:12-6; discussion 30-2.
  6. BCSH guideline for the use of anti-D immunoglobulin for the prevention of haemolytic disease of the fetus and newborn; British Committee for Standards in Haematology (Jan 2014)
  7. Preterm labour and birth; NICE Guidelines (November 2015 - last updated June 2022)
  8. Downes KL, Grantz KL, Shenassa ED; Maternal, Labor, Delivery, and Perinatal Outcomes Associated with Placental Abruption: A Systematic Review. Am J Perinatol. 2017 Aug;34(10):935-957. doi: 10.1055/s-0037-1599149. Epub 2017 Mar 22.
  9. Bhandari S, Raja EA, Shetty A, et al; Maternal and perinatal consequences of antepartum haemorrhage of unknown origin. BJOG. 2014 Jan;121(1):44-50; discussion 50-2. doi: 10.1111/1471-0528.12464. Epub 2013 Oct 15.

Article history

The information on this page is written and peer reviewed by qualified clinicians.

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