Overview
These conditions fall into three clinical groups:
| Group | Conditions |
|---|
| Bleeding after birth | Postpartum hemorrhage |
| Early-pregnancy complications | Molar pregnancy, miscarriage (spontaneous abortion), ectopic pregnancy |
| Bleeding in the second half of pregnancy | Placenta previa, placental abruption, vasa previa |
Emergency warning: Heavy bleeding, severe one-sided or generalized abdominal pain, shoulder-tip pain, dizziness/fainting, fever after pregnancy loss, rupture of membranes with bleeding, or reduced fetal movements require urgent obstetric assessment.
1. Postpartum hemorrhage
Definition
Postpartum hemorrhage (PPH) is excessive bleeding after childbirth.
- A common modern definition is cumulative blood loss of at least 1,000 mL, or any blood loss with signs/symptoms of hypovolemia, within 24 hours after birth.
- Primary PPH: within the first 24 hours after delivery.
- Secondary PPH: from 24 hours to 6 weeks postpartum.
Pregnancy increases circulating blood volume, so a woman may lose a large amount of blood before becoming hypotensive. Early tachycardia, pallor, dizziness, reduced urine output, or altered consciousness are important warning signs.
Causes: the “4 Ts”
| Cause | Meaning | Examples |
|---|
| Tone | Uterus fails to contract | Uterine atony, the commonest cause |
| Trauma | Genital-tract injury | Cervical/vaginal/perineal tear, uterine rupture, uterine inversion |
| Tissue | Retained or abnormally adherent placental tissue | Retained placenta, retained products, placenta accreta spectrum |
| Thrombin | Coagulation disorder | DIC, severe abruption, inherited bleeding disorder, anticoagulation |
Uterine atony
Normally, contraction of uterine muscle fibers compresses the blood vessels at the placental bed, termed the “living ligature” mechanism. In uterine atony, the uterus remains soft and poorly contracted, so these vessels bleed freely.
Risk factors
- Overdistended uterus: multiple pregnancy, polyhydramnios, macrosomia
- Prolonged or very rapid labor
- Oxytocin exposure or uterine muscle fatigue
- Chorioamnionitis
- Grand multiparity
- Magnesium sulfate or some anesthetic agents
- Retained placenta
- Prior PPH
Recognition
- Excessive vaginal bleeding
- Boggy, enlarged uterus, especially in atony
- Continued bleeding despite uterine massage
- Tachycardia, hypotension, pallor, confusion
- A firm uterus with bleeding suggests trauma or retained tissue rather than atony.
Immediate management
PPH must be treated as a simultaneous resuscitation and cause-control emergency.
- Call for help: obstetric, anesthesia, blood bank, operating theatre staff.
- Assess ABCs: airway, breathing, circulation; give oxygen if needed.
- Two large-bore IV cannulas.
- Send blood for CBC, group and crossmatch, coagulation tests, fibrinogen, electrolytes, and blood gas where appropriate.
- Begin rapid warmed crystalloid while arranging blood products; activate a massive transfusion protocol for severe hemorrhage.
- Quantify blood loss and monitor pulse, blood pressure, urine output, mental state, and temperature.
- Identify the cause using the 4 Ts.
If uterine atony is suspected
- Empty the bladder.
- Perform uterine massage and bimanual uterine compression.
- Start a uterotonic, usually oxytocin.
- Add further uterotonics depending on contraindications:
- Ergometrine/methylergometrine: avoid in hypertension or preeclampsia.
- Carboprost: avoid in asthma and use cautiously in cardiac, hepatic, or renal disease.
- Misoprostol: may be used when injectable uterotonics are unavailable or as an adjunct.
- Give tranexamic acid (TXA) as early as possible and within 3 hours of birth for established PPH, unless contraindicated. The 2024 individual-patient meta-analysis supports early TXA treatment without an apparent increase in thromboembolic events in trial populations (Ker et al., 2024).
If bleeding continues
- Inspect the cervix, vagina, and perineum and repair lacerations.
- Manually remove retained placenta or retained tissue when indicated.
- Give blood components guided by clinical bleeding and laboratory results. In severe PPH, early attention to fibrinogen is important.
- Use uterine balloon tamponade if bleeding from atony persists despite first-line measures and appropriate resources are available.
- Escalate to surgical/interventional treatment:
- Compression sutures, such as B-Lynch suture
- Uterine artery ligation or internal iliac artery ligation
- Uterine artery embolization, if stable and rapidly available
- Hysterectomy if hemorrhage is uncontrollable or placenta accreta spectrum is present
The current
WHO PPH guideline emphasizes standardized treatment bundles using uterotonics, TXA, IV fluids, assessment for trauma/tissue, monitoring, and escalation where needed.
Secondary PPH
Usually caused by:
- Retained products of conception
- Infection, especially endometritis
- Subinvolution of the placental site
- Breakdown/infection of genital-tract wounds
- Less commonly, a coagulation disorder
Assessment includes examination, ultrasound when indicated, CBC, infection assessment, antibiotics if infection is suspected, and uterine evacuation only when clinically indicated.
Prevention
- Identify antenatal risk factors.
- Active management of the third stage of labor.
- Prophylactic uterotonic, commonly oxytocin, after delivery.
- Deliver high-risk patients where blood products, anesthesia, surgery, and critical care are available.
2. Molar pregnancy
Definition
A molar pregnancy, also called a hydatidiform mole, is an abnormal gestation caused by abnormal fertilization and abnormal trophoblastic proliferation. The placental chorionic villi become swollen and cystic, producing a grape-like appearance.
It is part of gestational trophoblastic disease (GTD). Some cases persist as gestational trophoblastic neoplasia (GTN), which needs oncology follow-up and chemotherapy.
Types
| Feature | Complete mole | Partial mole |
|---|
| Fetal tissue | Absent | Often present but abnormal/nonviable |
| Genetic pattern | Usually androgenetic diploid, commonly 46,XX | Usually triploid, commonly 69,XXY |
| Fertilization | Empty ovum fertilized, with paternal genome duplication or two sperm | Normal ovum fertilized by two sperm |
| Trophoblastic proliferation | Diffuse and marked | Focal, less marked |
| hCG | Often markedly elevated | Less markedly elevated |
| Uterine size | Often larger than dates | Often normal or smaller than dates |
| Persistent GTN risk | Higher | Lower |
A complete mole has paternal genetic material with no viable embryo. A partial mole has an abnormal triploid conceptus and may resemble a missed or incomplete miscarriage. Berek & Novak describes complete moles as typically androgenetic diploid and partial moles as typically triploid.
Risk factors
- Previous molar pregnancy
- Extremes of maternal age, especially very young or older reproductive age
- Prior pregnancy loss in some populations
- Rare familial recurrent molar pregnancy syndromes
Clinical features
- Vaginal bleeding in the first trimester
- Uterus larger than expected for dates, especially in complete mole
- Excessive nausea/vomiting due to high hCG
- Passage of grape-like vesicles, now uncommon because diagnosis is often earlier
- Early-onset preeclampsia, especially before 20 weeks
- Hyperthyroid features: tremor, tachycardia, heat intolerance
- Theca-lutein ovarian cysts
- No fetal heart activity in complete mole
Diagnosis
- Quantitative serum β-hCG
- Transvaginal ultrasound
- Complete mole: diffuse echogenic intrauterine mass with multiple small cystic spaces, classically “snowstorm” appearance; no fetus.
- Partial mole: may show gestational sac/fetal tissue with cystic placental changes.
- Histopathology after evacuation confirms the diagnosis.
- Baseline assessment may include CBC, blood group/Rh status, renal/liver function, thyroid function if clinically indicated, and chest imaging if GTN is suspected.
Management
Initial treatment
- Stabilize if heavy bleeding or severe hyperemesis/preeclampsia occurs.
- Suction evacuation/curettage is usually the preferred fertility-preserving treatment.
- Send all tissue for histopathology.
- Give anti-D immunoglobulin to an unsensitized Rh-negative patient according to local guidance.
- Hysterectomy may be considered in selected patients who do not desire fertility, but it does not remove the need for hCG follow-up.
hCG surveillance
Serial quantitative hCG measurement is essential because hCG should progressively fall to normal after complete evacuation.
Persistent or rising hCG may indicate postmolar GTN.
Features suggesting GTN
- hCG level plateaus over serial measurements
- hCG rises over serial measurements
- hCG remains detectable for a prolonged period
- Histologic choriocarcinoma
- Metastatic disease
Patients should avoid pregnancy during the surveillance interval because a new pregnancy raises hCG and makes recurrence/persistence difficult to detect. Use reliable contraception as advised by the treating trophoblastic-disease center.
Prognosis
Most molar pregnancies resolve after evacuation and surveillance. GTN is highly treatable, including many metastatic cases, when identified promptly.
3. Abortion / miscarriage
Terminology
In clinical obstetrics, spontaneous abortion means miscarriage, or spontaneous loss of an intrauterine pregnancy before fetal viability. The gestational-age threshold differs by country, often before 20 to 24 weeks.
“Abortion” can also refer to induced termination of pregnancy, but the conditions below refer to spontaneous miscarriage.
Main causes
Most first-trimester miscarriages are caused by fetal chromosomal abnormalities. Other contributors include:
- Uterine anomalies
- Antiphospholipid syndrome
- Uncontrolled diabetes or thyroid disease
- Severe infection, though less common
- Cervical insufficiency in later losses
- Lifestyle factors such as smoking
- Increasing maternal age
A single early miscarriage is common and usually does not mean infertility or a recurrent problem.
Types of miscarriage
| Type | Cervix | Fetal cardiac activity / retained tissue | Typical features |
|---|
| Threatened miscarriage | Closed | Pregnancy may still be viable | Bleeding with or without mild cramps |
| Inevitable miscarriage | Open | Pregnancy cannot continue | Bleeding, cramps, dilated cervix |
| Incomplete miscarriage | Open | Some products expelled, some retained | Heavy bleeding, pain, retained tissue |
| Complete miscarriage | Closed after expulsion | Uterus empty or nearly empty | Bleeding/pain settle after tissue passes |
| Missed miscarriage | Usually closed | Nonviable intrauterine pregnancy retained | Minimal bleeding or no symptoms |
| Septic miscarriage | Variable | Infected retained tissue may be present | Fever, uterine tenderness, foul discharge, systemic illness |
| Recurrent pregnancy loss | Not a clinical type of acute miscarriage | Usually defined by repeated losses | Requires targeted evaluation |
Evaluation
- Assess hemodynamic stability: pulse, blood pressure, ongoing blood loss.
- Ask about pain, bleeding, tissue passage, fever, pregnancy dates, ectopic risk factors, and Rh status.
- Perform abdominal and pelvic examination when appropriate.
- Transvaginal ultrasound to establish intrauterine pregnancy, viability, retained tissue, and exclude ectopic pregnancy.
- Quantitative β-hCG may be repeated if ultrasound findings are inconclusive.
- CBC and blood group/Rh testing if bleeding is significant.
A pregnancy of uncertain viability or pregnancy of unknown location should not be labeled miscarriage prematurely. Repeat ultrasound and serial hCG can be necessary.
Management
Threatened miscarriage
- Confirm viability and exclude ectopic pregnancy.
- Expectant management and safety-net advice are common.
- Progesterone may be considered in selected women with early bleeding and a history of previous miscarriage, depending on local protocol.
- Advise urgent review for increasing pain, bleeding, syncope, or fever.
Complete miscarriage
- Usually needs no uterine intervention if the patient is stable, bleeding has settled, and ultrasound/clinical assessment supports complete passage.
- Follow-up confirms symptom resolution and, when needed, hCG decline.
Incomplete or missed miscarriage
Three options are generally available if the patient is stable and infection is absent:
-
Expectant management
Allowing spontaneous passage of tissue.
-
Medical management
Usually with misoprostol, sometimes preceded by mifepristone depending on guideline and availability.
-
Surgical uterine evacuation
Vacuum aspiration or suction curettage. It is indicated sooner for hemodynamic instability, heavy uncontrolled bleeding, infection, suspected molar pregnancy, or patient preference.
Septic miscarriage
This is an emergency.
- Broad-spectrum IV antibiotics
- IV fluids and resuscitation
- Prompt uterine evacuation once stabilized
- Culture tests and management of sepsis
- Escalation to critical care if shock or organ dysfunction occurs
Rh prophylaxis
Give anti-D immunoglobulin to unsensitized Rh-negative patients according to gestation, bleeding severity, and local guidance, particularly after surgical management or later first-trimester/second-trimester loss.
Recurrent pregnancy loss
Repeated miscarriages merit evaluation for:
- Antiphospholipid syndrome
- Uterine cavity abnormalities
- Parental chromosomal rearrangements in selected cases
- Thyroid disease and diabetes where relevant
- Products-of-conception genetic testing in selected cases
4. Placenta previa
Definition
Placenta previa occurs when the placenta implants in the lower uterine segment and lies over, partially over, or very close to the internal cervical os.
Current ultrasound reporting commonly describes:
- Placenta previa: placenta covers the internal os.
- Low-lying placenta: placental edge is close to, but does not cover, the internal os.
Older classifications include complete, partial, and marginal previa.
Pathophysiology
As the lower uterine segment stretches in late pregnancy and the cervix begins to efface/dilate, the placental attachment may shear. This causes maternal bleeding from the placental bed.
Risk factors
- Previous cesarean birth
- Previous placenta previa
- Prior uterine surgery or curettage
- Multiparity
- Multiple pregnancy
- Advanced maternal age
- Smoking or cocaine use
- Assisted reproduction
A placenta previa with a prior cesarean scar increases concern for placenta accreta spectrum, in which the placenta is abnormally adherent or invasive.
Clinical features
- Painless, bright-red vaginal bleeding in the second half of pregnancy
- Bleeding may stop and recur
- Usually a soft, non-tender uterus
- Fetal malpresentation, particularly breech or transverse lie, may occur
Diagnosis
- Ultrasound establishes placental location.
- Transvaginal ultrasound is safe and provides the most accurate assessment of the relationship between placenta and internal os.
- A low placenta identified at the mid-pregnancy scan often resolves later because expansion of the lower uterine segment moves the placental edge away from the os.
Critical precaution
Do not perform a digital vaginal examination until placenta previa has been excluded by ultrasound. A digital examination can disrupt placental attachment and trigger severe hemorrhage.
Management
Acute bleeding
- Maternal stabilization: two IV lines, CBC, coagulation screen, blood group/crossmatch.
- Continuous fetal assessment if gestation is viable.
- Ultrasound assessment.
- Anti-D for Rh-negative unsensitized patients as appropriate.
- Obstetric consultation and admission if bleeding is significant or recurrent.
Ongoing care
Management depends on:
- Amount and recurrence of bleeding
- Gestational age
- Placental position
- Fetal status
- Labor or rupture of membranes
- Access to emergency care
A patient with persistent placenta previa generally requires cesarean birth, often planned before labor begins. Timing is individualized based on bleeding and maternal-fetal status. Heavy ongoing bleeding, maternal instability, labor with significant previa, or fetal compromise requires urgent delivery.
5. Placental abruption
Definition
Placental abruption, or abruptio placentae, is premature separation of a normally implanted placenta from the uterine wall before birth.
Bleeding can be:
- Revealed: blood exits through the vagina.
- Concealed: blood accumulates behind the placenta, so visible bleeding may be minimal despite severe maternal and fetal compromise.
- Mixed: both concealed and vaginal bleeding occur.
Pathophysiology
Separation of the placenta causes bleeding into the decidua and behind the placenta. This reduces placental gas/nutrient exchange, causing fetal hypoxia. Severe abruption can consume clotting factors and trigger DIC.
Risk factors
- Hypertension, preeclampsia
- Previous abruption
- Maternal trauma, including road traffic collision or intimate-partner violence
- Cocaine use and smoking
- Prelabor rupture of membranes
- Chorioamnionitis
- Multifetal pregnancy
- Sudden uterine decompression, such as after rupture of membranes with polyhydramnios
- Thrombophilia in selected cases
Clinical features
- Painful vaginal bleeding
- Constant abdominal pain or back pain
- Uterine tenderness
- Tense, rigid, “board-like” uterus
- Frequent uterine contractions
- Reduced fetal movements
- Nonreassuring fetal heart tracing or fetal death in severe cases
- Maternal shock that seems disproportionate to visible bleeding, suggesting concealed hemorrhage
Not every abruption presents classically. It is largely a clinical diagnosis.
Diagnosis
- Maternal evaluation and fetal monitoring are central.
- CBC, blood group/crossmatch, coagulation tests, and especially fibrinogen.
- Ultrasound may demonstrate retroplacental hematoma, but a normal ultrasound does not rule out abruption.
- Continuous cardiotocography is used for viable pregnancies.
Complications
Maternal
- Massive hemorrhage and shock
- DIC
- Acute kidney injury
- PPH
- Need for hysterectomy in severe cases
- Maternal death, rarely
Fetal
- Hypoxia and acidosis
- Growth restriction in chronic abruption
- Preterm birth
- Stillbirth
Management
- Stabilize mother first.
- Two large-bore IV lines, blood products as required, and early obstetric/anesthetic involvement.
- Continuous fetal monitoring if viable.
- Correct coagulopathy with appropriate components.
- Administer anti-D for Rh-negative unsensitized patients where indicated.
- Immediate delivery is indicated for severe abruption, maternal instability, significant fetal compromise, or fetal death with maternal deterioration/coagulopathy.
- Vaginal birth may be appropriate if delivery is imminent or fetal death has occurred and the mother is stable.
- Cesarean birth is often needed for a live fetus with acute compromise when vaginal delivery is not imminent.
6. Vasa previa
Definition
Vasa previa occurs when unprotected fetal blood vessels run through the membranes over or very near the internal cervical os.
Unlike placenta previa, the threatened vessels are fetal vessels, not maternal placental tissue. When membranes rupture or the cervix dilates, these vessels can tear, causing rapid fetal hemorrhage.
Types
- Type 1: vessels from a velamentous cord insertion cross the lower uterine segment.
- Type 2: vessels connecting a succenturiate or bilobed placental lobe cross near the os.
Risk factors
- Velamentous cord insertion
- Succenturiate or bilobed placenta
- Low-lying placenta or resolved placenta previa
- Multiple pregnancy
- In vitro fertilization/assisted reproduction
Clinical features
Antenatally, the mother may have no symptoms.
The classic intrapartum presentation is:
- Rupture of membranes
- Sudden painless vaginal bleeding
- Acute fetal bradycardia or sinusoidal fetal heart tracing
The blood loss is fetal. Even a relatively small volume can be catastrophic because fetal blood volume is limited.
Diagnosis
- Antenatal diagnosis is made with transvaginal ultrasound plus color Doppler.
- The goal is to identify fetal vessels crossing or close to the internal os before labor or membrane rupture.
Management
- Refer to maternal-fetal medicine/obstetric care.
- Avoid labor and membrane rupture.
- Plan cesarean birth before spontaneous labor, often in the late preterm period, with timing individualized to risk and local protocol.
- Corticosteroids may be considered if preterm birth is expected.
- In suspected vasa previa with bleeding and fetal heart-rate abnormality after membrane rupture, perform immediate emergency cesarean delivery and prepare neonatal resuscitation/transfusion.
Key distinction
Vasa previa is especially dangerous because the mother may appear relatively stable while the fetus rapidly exsanguinates.
7. Ectopic pregnancy
Definition
An ectopic pregnancy implants outside the endometrial cavity. Most are in the fallopian tube, especially the ampullary portion.
Other sites include:
- Interstitial/cornual region
- Cervix
- Cesarean-scar pregnancy
- Ovary
- Abdominal cavity
- Heterotopic pregnancy: simultaneous intrauterine and ectopic pregnancies, more likely after assisted reproduction
Risk factors
- Previous ectopic pregnancy
- Tubal surgery or sterilization
- Pelvic inflammatory disease, especially chlamydial infection
- Endometriosis
- Assisted reproductive technology
- Smoking
- Intrauterine device failure: pregnancy is rare with an IUD, but if pregnancy occurs, the relative likelihood of ectopic implantation is higher
- Prior abdominal/pelvic surgery
Many patients have no identifiable risk factor.
Clinical presentation
Typical symptoms occur at 6 to 10 weeks:
- Amenorrhea or positive pregnancy test
- Vaginal spotting/bleeding
- Unilateral lower abdominal or pelvic pain
Features of rupture/hemoperitoneum:
- Severe abdominal pain
- Shoulder-tip pain from diaphragmatic irritation
- Syncope, dizziness, weakness
- Peritoneal signs
- Hypotension or shock
- Abdominal distension
A ruptured ectopic pregnancy is a life-threatening emergency. Absence of hypotension does not exclude significant internal bleeding.
Diagnosis
Pregnancy test
A positive pregnancy test confirms pregnancy but not its location.
Transvaginal ultrasound
Possible findings:
- Definite intrauterine pregnancy excludes ectopic pregnancy in most spontaneous conceptions, but not heterotopic pregnancy.
- Adnexal mass separate from the ovary
- Extrauterine gestational sac/yolk sac/fetal pole
- Free pelvic or intraperitoneal fluid, particularly concerning when significant
Serial quantitative β-hCG
If ultrasound does not identify an intrauterine or ectopic pregnancy, the condition is called a pregnancy of unknown location.
Serial hCG trends and repeat ultrasound are used, but hCG alone should not be used to diagnose ectopic pregnancy or to give methotrexate to a potentially viable intrauterine pregnancy.
Management
1. Emergency surgical management
Required for:
- Hemodynamic instability
- Suspected or confirmed rupture
- Peritoneal signs or significant hemoperitoneum
- Contraindication to methotrexate
- Inability to attend follow-up
- Often, high hCG, fetal cardiac activity outside the uterus, or a large ectopic mass, depending on circumstances
Surgery is generally laparoscopic if the patient is stable. Procedures include:
- Salpingectomy: removal of affected tube
- Salpingostomy: incision to remove ectopic tissue while preserving the tube in selected cases
2. Methotrexate medical treatment
Methotrexate stops trophoblastic cell growth. It may be suitable when the patient:
- Is hemodynamically stable
- Has no evidence of rupture
- Can reliably attend serial hCG monitoring
- Has no contraindication to methotrexate
Contraindications include significant liver, renal, or hematologic disease, immunodeficiency, breastfeeding, certain active pulmonary/hepatic disease, and inability to follow up. Regimens differ, but all require hCG monitoring until the level becomes undetectable.
The risk of rupture continues until hCG resolves. ACOG notes that nonruptured tubal ectopic pregnancy can often be treated with methotrexate, but an unstable patient needs prompt surgery (
ACOG tubal ectopic guidance).
3. Expectant management
Rarely appropriate when:
- Patient is stable and asymptomatic
- hCG is very low and falling
- No concerning ultrasound findings
- Reliable follow-up is available
Follow-up and future fertility
- Follow hCG to resolution after methotrexate and after salpingostomy.
- Advise urgent review for worsening pain, shoulder pain, fainting, or heavy bleeding.
- Future intrauterine pregnancy is possible, but risk of recurrent ectopic pregnancy is increased.
- Early ultrasound in the next pregnancy is appropriate to confirm intrauterine implantation.
High-yield comparison: bleeding in late pregnancy
| Feature | Placenta previa | Placental abruption | Vasa previa |
|---|
| Main source of bleeding | Maternal placental bed | Maternal placental bed behind placenta | Fetal vessels |
| Pain | Usually painless | Usually painful | Usually painless |
| Uterus | Soft, non-tender | Tender, hypertonic, possibly rigid | Usually soft |
| Bleeding | Bright red, may recur | Variable, may be concealed | Often occurs at membrane rupture |
| Fetal compromise | Possible if major bleed | Common in severe cases | Sudden, profound, often immediate |
| Vaginal examination | Avoid digital exam until ultrasound excludes previa | Examination only as clinically appropriate after assessment | Avoid membrane rupture/labor if diagnosed |
| Typical delivery approach | Cesarean if placenta covers os | Depends on maternal/fetal status and labor progress | Planned cesarean before labor; emergency cesarean if bleeding/rupture occurs |
Recent-evidence note
The medical-library descriptions are consistent with recent evidence, but PPH guidance has been updated since older textbook editions. In particular, the
WHO 2025 consolidated PPH guidance and the TXA meta-analysis, PMID
39461793, should guide current clinical practice alongside local obstetric protocols.