Third trimester bleeding: Difference between revisions
Ostermayer (talk | contribs) (Created page with "==Background== *Third trimester bleeding (also termed antepartum hemorrhage) refers to vaginal bleeding occurring after 28 weeks gestational age through delivery<ref name="sakornbut">Sakornbut E, Leeman L, Fontaine P. Late pregnancy bleeding. ''Am Fam Physician''. 2007;75(8):1199-1206.</ref> *Complicates 2–5% of all pregnancies<ref name="sakornbut"/> *Is an obstetric emergency associated with significant maternal and fetal morbidity and mortality<ref name="gandhi">Gand...") |
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==Evaluation== | ==Evaluation== | ||
===Workup=== | ===Workup=== | ||
* | *Primary survey and maternal stabilization | ||
**ABCs; two large-bore IVs, crystalloid resuscitation<ref name="muench"/> | **ABCs; two large-bore IVs, crystalloid resuscitation<ref name="muench"/> | ||
**Continuous maternal vital sign monitoring | **Continuous maternal vital sign monitoring | ||
**Left lateral uterine displacement | **Left lateral uterine displacement | ||
* | *Laboratory studies | ||
**CBC (serial hematocrit) | **CBC (serial hematocrit) | ||
**Type and crossmatch (or at minimum type and screen) | **Type and crossmatch (or at minimum type and screen) | ||
| Line 72: | Line 72: | ||
**Metabolic panel | **Metabolic panel | ||
**[[Kleihauer-Betke test]] — especially if Rh-negative to calculate RhoGAM dosing | **[[Kleihauer-Betke test]] — especially if Rh-negative to calculate RhoGAM dosing | ||
* | *Fetal assessment | ||
**Continuous electronic fetal heart rate monitoring and tocometry | **Continuous electronic fetal heart rate monitoring and tocometry | ||
**Category III fetal heart rate tracings (absent variability with recurrent late/variable decelerations, bradycardia, or sinusoidal pattern) warrant emergent delivery | **Category III fetal heart rate tracings (absent variability with recurrent late/variable decelerations, bradycardia, or sinusoidal pattern) warrant emergent delivery | ||
* | *Imaging | ||
**Transabdominal ultrasound to assess: | **Transabdominal ultrasound to assess: | ||
***Placental location (rule out previa before any digital vaginal exam) | ***Placental location (rule out previa before any digital vaginal exam) | ||
| Line 83: | Line 83: | ||
===Diagnosis=== | ===Diagnosis=== | ||
* | *Placental abruption is primarily a '''clinical diagnosis'''; ultrasound has poor sensitivity (25–50%) because acute hemorrhage may be isoechoic to placental tissue<ref name="brandt"/> | ||
* | *Placenta previa is diagnosed on ultrasound (transabdominal or transvaginal) | ||
* | *Vasa previa is diagnosed by transvaginal ultrasound with color Doppler demonstrating fetal vessels over the internal os, confirmed with pulse-wave Doppler showing fetal heart rate waveform<ref name="oyelese"/> | ||
* | *Uterine rupture is a clinical diagnosis; ultrasound may show free fluid, abnormal fetal lie, or absent myometrium, but operative findings are often required for confirmation<ref name="patel"/> | ||
* | *Apt test (alkali denaturation test) can distinguish fetal from maternal blood when the source of bleeding is uncertain; fetal hemoglobin (HbF) resists alkali denaturation and remains pink, while adult hemoglobin (HbA) denatures and turns brown | ||
====Critical Rule==== | ====Critical Rule==== | ||
| Line 94: | Line 94: | ||
==Management== | ==Management== | ||
* | *Resuscitation | ||
**IV access with two large-bore (16–18 gauge) catheters | **IV access with two large-bore (16–18 gauge) catheters | ||
**Aggressive crystalloid resuscitation; initiate massive transfusion protocol if hemodynamically unstable | **Aggressive crystalloid resuscitation; initiate massive transfusion protocol if hemodynamically unstable | ||
**Correct coagulopathy with blood products (pRBCs, FFP, cryoprecipitate, platelets) as indicated | **Correct coagulopathy with blood products (pRBCs, FFP, cryoprecipitate, platelets) as indicated | ||
* | *Rh immunoglobulin | ||
**Administer [[RhoGAM]] (300 mcg) to all Rh-negative mothers | **Administer [[RhoGAM]] (300 mcg) to all Rh-negative mothers | ||
**Additional doses guided by Kleihauer-Betke quantification | **Additional doses guided by Kleihauer-Betke quantification | ||
* | *Fetal monitoring | ||
**Continuous electronic fetal monitoring; ensure immediate operative delivery capability | **Continuous electronic fetal monitoring; ensure immediate operative delivery capability | ||
* | *Condition-specific management | ||
** | **Placental abruption | ||
***Mild, with reassuring fetal status and preterm gestation: close inpatient observation, serial labs, consider antenatal corticosteroids if < 37 weeks | ***Mild, with reassuring fetal status and preterm gestation: close inpatient observation, serial labs, consider antenatal corticosteroids if < 37 weeks | ||
***Moderate-to-severe abruption, maternal instability, or nonreassuring fetal status: emergent delivery<ref name="brandt"/> | ***Moderate-to-severe abruption, maternal instability, or nonreassuring fetal status: emergent delivery<ref name="brandt"/> | ||
***If fetal demise has occurred, vaginal delivery is generally preferred to minimize maternal surgical morbidity<ref name="sakornbut"/> | ***If fetal demise has occurred, vaginal delivery is generally preferred to minimize maternal surgical morbidity<ref name="sakornbut"/> | ||
***DIC: correct coagulopathy aggressively; target fibrinogen > 150–200 mg/dL | ***DIC: correct coagulopathy aggressively; target fibrinogen > 150–200 mg/dL | ||
** | **Placenta previa | ||
***If stable, not actively hemorrhaging, and preterm: inpatient observation, antenatal corticosteroids, plan for cesarean delivery at 36–37 weeks<ref name="sakornbut"/> | ***If stable, not actively hemorrhaging, and preterm: inpatient observation, antenatal corticosteroids, plan for cesarean delivery at 36–37 weeks<ref name="sakornbut"/> | ||
***Active hemorrhage or maternal/fetal instability: emergent cesarean delivery | ***Active hemorrhage or maternal/fetal instability: emergent cesarean delivery | ||
***Tocolysis may be considered cautiously if preterm with contractions contributing to bleeding<ref name="sakornbut"/> | ***Tocolysis may be considered cautiously if preterm with contractions contributing to bleeding<ref name="sakornbut"/> | ||
** | **Vasa previa | ||
***Known diagnosis: planned cesarean delivery at 34–37 weeks of gestation<ref name="smfm">Society for Maternal-Fetal Medicine (SMFM); Sinkey RG, Odibo AO, Dashe JS. #37: Diagnosis and management of vasa previa. ''Am J Obstet Gynecol''. 2015;213(5):615-619. PMID 26292048.</ref> | ***Known diagnosis: planned cesarean delivery at 34–37 weeks of gestation<ref name="smfm">Society for Maternal-Fetal Medicine (SMFM); Sinkey RG, Odibo AO, Dashe JS. #37: Diagnosis and management of vasa previa. ''Am J Obstet Gynecol''. 2015;213(5):615-619. PMID 26292048.</ref> | ||
***Acute bleeding with rupture of fetal vessels: emergent cesarean delivery and preparation for neonatal transfusion | ***Acute bleeding with rupture of fetal vessels: emergent cesarean delivery and preparation for neonatal transfusion | ||
** | **Uterine rupture | ||
***Emergent cesarean delivery/laparotomy<ref name="patel"/> | ***Emergent cesarean delivery/laparotomy<ref name="patel"/> | ||
***Uterine repair versus hysterectomy depending on extent of injury, hemodynamic stability, and future fertility desires | ***Uterine repair versus hysterectomy depending on extent of injury, hemodynamic stability, and future fertility desires | ||
***Aggressive resuscitation and blood product administration | ***Aggressive resuscitation and blood product administration | ||
* | *Antenatal corticosteroids | ||
**Administer betamethasone or dexamethasone for fetal lung maturity if 23–36+6 weeks gestation and delivery is anticipated, but do not delay emergent delivery for steroid administration<ref name="gyamfi">Gyamfi-Bannerman C. Society for Maternal-Fetal Medicine (SMFM) Consult Series #44: Management of bleeding in the late preterm period. ''Am J Obstet Gynecol''. 2018;218(1):B2-B8.</ref> | **Administer betamethasone or dexamethasone for fetal lung maturity if 23–36+6 weeks gestation and delivery is anticipated, but do not delay emergent delivery for steroid administration<ref name="gyamfi">Gyamfi-Bannerman C. Society for Maternal-Fetal Medicine (SMFM) Consult Series #44: Management of bleeding in the late preterm period. ''Am J Obstet Gynecol''. 2018;218(1):B2-B8.</ref> | ||
* | *MgSO4 for neuroprotection | ||
**Consider magnesium sulfate for fetal neuroprotection if < 32 weeks gestation and delivery is imminent | **Consider magnesium sulfate for fetal neuroprotection if < 32 weeks gestation and delivery is imminent | ||
Latest revision as of 16:15, 19 March 2026
Background
- Third trimester bleeding (also termed antepartum hemorrhage) refers to vaginal bleeding occurring after 28 weeks gestational age through delivery[1]
- Complicates 2–5% of all pregnancies[1]
- Is an obstetric emergency associated with significant maternal and fetal morbidity and mortality[2]
- The two most common causes — placental abruption and placenta previa — account for approximately half of all cases[2]
- The remaining cases are attributable to less common etiologies (vasa previa, uterine rupture, cervical pathology) or remain unexplained
- The physiologic hypervolemia of pregnancy (30–50% increase in blood volume) may mask early signs of hemorrhagic shock, and clinicians should be aware that significant blood loss can occur before vital sign derangements appear[3]
Clinical Features
General
- Vaginal bleeding — ranges from light spotting to massive hemorrhage; may be bright red, dark, or mixed with amniotic fluid
- Bleeding may be partially or completely concealed (e.g. in abruption)
- Abdominal or pelvic pain, uterine tenderness, or contractions may be present depending on etiology
- Signs of hemodynamic instability (tachycardia, hypotension, pallor, altered mental status) in severe cases
- Abnormal fetal heart rate patterns
By Etiology
Placental Abruption
- Most common cause of painful third trimester bleeding
- Classic triad: vaginal bleeding, abdominal/uterine pain, uterine contractions[4]
- Uterus often tender and hypertonic ("woody" or "board-like")
- Concealed hemorrhage may present without vaginal bleeding but with pain, uterine irritability, and fetal distress[4]
- May be complicated by DIC in ~10% of cases (more common with fetal death)[1]
- Risk factors: hypertension/preeclampsia, trauma, cocaine use, tobacco use, prior abruption, PPROM, advanced maternal age, multiparity
Placenta Previa
- Classic presentation is painless, bright red vaginal bleeding
- May have an initial "sentinel bleed" that is not immediately life-threatening[1]
- Bleeding may become profuse without warning
- Uterus is typically soft and non-tender
- Risk factors: prior cesarean delivery, prior previa, multiparity, advanced maternal age, smoking, IVF, multiple gestation
Vasa Previa
- Rare (~1 per 2,500 deliveries) but carries very high fetal mortality when undiagnosed[5]
- Onset of vaginal bleeding typically coincides with rupture of membranes
- Bleeding is of fetal origin; even small-volume blood loss can cause rapid fetal exsanguination
- Fetal heart rate tracing may show sinusoidal pattern or acute bradycardia
- Risk factors: velamentous cord insertion, bilobed/succenturiate placenta, low-lying placenta, IVF, multiple gestation[5]
Uterine Rupture
- Most commonly occurs in women with prior uterine surgery (especially prior cesarean section) during trial of labor[6]
- Presentation may include sudden severe abdominal pain, vaginal bleeding, loss of fetal station, cessation of contractions, and maternal hemodynamic instability
- Fetal bradycardia is often the earliest and most consistent sign[7]
- Fetal parts may become palpable through the abdomen
- Risk factors: prior cesarean section (especially classical incision), myomectomy, uterine instrumentation, labor induction/augmentation, grand multiparity
Differential Diagnosis
- Placental Abruption
- Placenta Previa
- Vasa Previa
- Uterine Rupture
- Cervicitis / cervical lesion (polyp, ectropion, cancer)
- Bloody show / normal labor onset
- Chorioamnionitis
- Cervical or vaginal trauma
- Coagulopathy (inherited or acquired)
- Intrauterine fetal demise
- Marginal sinus rupture
- Placenta accreta spectrum
Evaluation
Workup
- Primary survey and maternal stabilization
- ABCs; two large-bore IVs, crystalloid resuscitation[3]
- Continuous maternal vital sign monitoring
- Left lateral uterine displacement
- Laboratory studies
- CBC (serial hematocrit)
- Type and crossmatch (or at minimum type and screen)
- Coagulation panel: PT/INR, PTT, fibrinogen — screen for DIC
- Fibrinogen < 200 mg/dL is concerning for consumptive coagulopathy
- Metabolic panel
- Kleihauer-Betke test — especially if Rh-negative to calculate RhoGAM dosing
- Fetal assessment
- Continuous electronic fetal heart rate monitoring and tocometry
- Category III fetal heart rate tracings (absent variability with recurrent late/variable decelerations, bradycardia, or sinusoidal pattern) warrant emergent delivery
- Imaging
- Transabdominal ultrasound to assess:
- Placental location (rule out previa before any digital vaginal exam)
- Retroplacental hematoma (though sensitivity for abruption is limited)
- Fetal presentation, viability, and amniotic fluid volume
- Transvaginal ultrasound with color Doppler if vasa previa suspected[5]
- Transabdominal ultrasound to assess:
Diagnosis
- Placental abruption is primarily a clinical diagnosis; ultrasound has poor sensitivity (25–50%) because acute hemorrhage may be isoechoic to placental tissue[4]
- Placenta previa is diagnosed on ultrasound (transabdominal or transvaginal)
- Vasa previa is diagnosed by transvaginal ultrasound with color Doppler demonstrating fetal vessels over the internal os, confirmed with pulse-wave Doppler showing fetal heart rate waveform[5]
- Uterine rupture is a clinical diagnosis; ultrasound may show free fluid, abnormal fetal lie, or absent myometrium, but operative findings are often required for confirmation[7]
- Apt test (alkali denaturation test) can distinguish fetal from maternal blood when the source of bleeding is uncertain; fetal hemoglobin (HbF) resists alkali denaturation and remains pink, while adult hemoglobin (HbA) denatures and turns brown
Critical Rule
- Do NOT perform a digital vaginal examination until placenta previa has been excluded by ultrasound — digital exam in the setting of previa can precipitate catastrophic hemorrhage[1]
- Sterile speculum exam may be performed to evaluate the cervix and assess the source/quantity of bleeding
Management
- Resuscitation
- IV access with two large-bore (16–18 gauge) catheters
- Aggressive crystalloid resuscitation; initiate massive transfusion protocol if hemodynamically unstable
- Correct coagulopathy with blood products (pRBCs, FFP, cryoprecipitate, platelets) as indicated
- Rh immunoglobulin
- Administer RhoGAM (300 mcg) to all Rh-negative mothers
- Additional doses guided by Kleihauer-Betke quantification
- Fetal monitoring
- Continuous electronic fetal monitoring; ensure immediate operative delivery capability
- Condition-specific management
- Placental abruption
- Mild, with reassuring fetal status and preterm gestation: close inpatient observation, serial labs, consider antenatal corticosteroids if < 37 weeks
- Moderate-to-severe abruption, maternal instability, or nonreassuring fetal status: emergent delivery[4]
- If fetal demise has occurred, vaginal delivery is generally preferred to minimize maternal surgical morbidity[1]
- DIC: correct coagulopathy aggressively; target fibrinogen > 150–200 mg/dL
- Placenta previa
- If stable, not actively hemorrhaging, and preterm: inpatient observation, antenatal corticosteroids, plan for cesarean delivery at 36–37 weeks[1]
- Active hemorrhage or maternal/fetal instability: emergent cesarean delivery
- Tocolysis may be considered cautiously if preterm with contractions contributing to bleeding[1]
- Vasa previa
- Known diagnosis: planned cesarean delivery at 34–37 weeks of gestation[8]
- Acute bleeding with rupture of fetal vessels: emergent cesarean delivery and preparation for neonatal transfusion
- Uterine rupture
- Emergent cesarean delivery/laparotomy[7]
- Uterine repair versus hysterectomy depending on extent of injury, hemodynamic stability, and future fertility desires
- Aggressive resuscitation and blood product administration
- Placental abruption
- Antenatal corticosteroids
- Administer betamethasone or dexamethasone for fetal lung maturity if 23–36+6 weeks gestation and delivery is anticipated, but do not delay emergent delivery for steroid administration[9]
- MgSO4 for neuroprotection
- Consider magnesium sulfate for fetal neuroprotection if < 32 weeks gestation and delivery is imminent
Disposition
- All patients with third trimester bleeding require emergent OB consultation
- Admit for observation at minimum; most patients will require inpatient monitoring
- Indications for emergent delivery include:
- Maternal hemodynamic instability despite resuscitation
- Category III fetal heart rate tracing in a viable fetus
- Massive hemorrhage
- Suspected uterine rupture
- Ruptured vasa previa
- If at a facility without obstetric/surgical capability, stabilize and arrange emergent transfer
- Ensure neonatal resuscitation team (NICU) is available or on standby for all deliveries
- Social work and emotional support services as needed, particularly in cases of fetal demise
See Also
- Placental Abruption
- Placenta Previa
- Vasa Previa
- Uterine Rupture
- Intrauterine fetal demise
- Vaginal Bleeding (Pregnant)
- DIC
- Postpartum hemorrhage
External Links
- Prompt evaluation and treatment of third-trimester bleeding - Clin Obstet Gynecol 2020
- Placental abruption at near-term and term gestations - Am J Obstet Gynecol 2023
- Vasa Previa - Obstet Gynecol 2023
- SMFM #37: Diagnosis and management of vasa previa - Am J Obstet Gynecol 2015
- Vaginal bleeding in late pregnancy - Emerg Med Clin North Am 2019
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 Sakornbut E, Leeman L, Fontaine P. Late pregnancy bleeding. Am Fam Physician. 2007;75(8):1199-1206.
- ↑ 2.0 2.1 Gandhi M, Guo W. Prompt evaluation and treatment of third-trimester bleeding. Clin Obstet Gynecol. 2020;63(4):751-760. PMID 33332831.
- ↑ 3.0 3.1 Muench MV, Canterino JC. Vaginal bleeding in late pregnancy. Emerg Med Clin North Am. 2019;37(2):251-264. PMID 30940370.
- ↑ 4.0 4.1 4.2 4.3 Brandt JS, Ananth CV. Placental abruption at near-term and term gestations: pathophysiology, epidemiology, diagnosis, and management. Am J Obstet Gynecol. 2023;228(5S):S1313-S1329. PMID 37164498.
- ↑ 5.0 5.1 5.2 5.3 Oyelese Y, Javinani A, Shamshirsaz AA. Vasa previa. Obstet Gynecol. 2023;142(3):503-518. PMID 37590981.
- ↑ Tanos V, Toney ZA. Uterine scar rupture – Prediction, prevention, diagnosis, and management. Best Pract Res Clin Obstet Gynaecol. 2019;59:115-131.
- ↑ 7.0 7.1 7.2 Patel RM, Kaler M, Al-Soufi S, et al. Diagnosis and management of uterine rupture in the third trimester of pregnancy: a case series and literature review. Cureus. 2023;15(6):e40060. PMID 37431303.
- ↑ Society for Maternal-Fetal Medicine (SMFM); Sinkey RG, Odibo AO, Dashe JS. #37: Diagnosis and management of vasa previa. Am J Obstet Gynecol. 2015;213(5):615-619. PMID 26292048.
- ↑ Gyamfi-Bannerman C. Society for Maternal-Fetal Medicine (SMFM) Consult Series #44: Management of bleeding in the late preterm period. Am J Obstet Gynecol. 2018;218(1):B2-B8.
