Intrauterine fetal demise: Difference between revisions
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==Background== | ==Background== | ||
*Defined as fetal death after 20 WGA | *Defined as fetal death after 20 WGA (weeks gestational age) | ||
**Prior to 20 WGA, fetal loss is classified as [[spontaneous abortion]] | |||
*Occurs in approximately 1 in 160 pregnancies | |||
*Risk increases with advancing gestational age | |||
*Most common causes include: | |||
**Placental abnormalities (e.g. [[Placental Abruption|abruption]], insufficiency) — most common identifiable cause | |||
**Chromosomal/genetic abnormalities | |||
**Maternal conditions ([[Preeclampsia|preeclampsia]], [[Diabetes in Pregnancy|diabetes in pregnancy]], [[Hypertension|chronic hypertension]], thrombophilias, autoimmune disease) | |||
**Umbilical cord abnormalities (knots, prolapse, compression) | |||
**Intrauterine infection (e.g. [[Chorioamnionitis|chorioamnionitis]], CMV, parvovirus B19, syphilis, listeria) | |||
**Fetal Hydrops | |||
**Cause remains unexplained in up to 25–60% of cases | |||
==Clinical Features== | ==Clinical Features== | ||
*Decreased or absent fetal movement (most common presenting complaint) | |||
*Vaginal bleeding (may or may not be present) | |||
*Uterine cramping or contractions | |||
*Absence of fetal heart tones on Doppler | |||
*Loss of pregnancy symptoms (e.g. breast tenderness, nausea) | |||
*Uterus may be small for gestational age | |||
*If prolonged fetal demise (retained > 3–4 weeks): | |||
**Signs/symptoms of [[Disseminated Intravascular Coagulation|DIC]] (bleeding, petechiae, ecchymosis) | |||
==Differential Diagnosis== | ==Differential Diagnosis== | ||
{{VB DDX greater than 20}} | |||
==Evaluation== | ==Evaluation== | ||
*Ultrasound | |||
**Absence of fetal cardiac activity on real-time ultrasound is diagnostic | |||
**Should be confirmed by two experienced operators if any uncertainty | |||
**Additional findings: overlapping skull bones (Spalding sign), soft tissue edema, echogenic amniotic fluid | |||
*Labs | |||
**[[CBC]] — evaluate for anemia, thrombocytopenia | |||
**[[Coagulation studies]] (PT/INR, PTT, fibrinogen) — screen for DIC | |||
***Risk of DIC increases significantly if fetus retained > 4 weeks | |||
***Fibrinogen < 200 mg/dL is concerning for consumptive coagulopathy | |||
**Type and screen (or crossmatch if actively bleeding) | |||
**[[Kleihauer-Betke test]] — to quantify fetomaternal hemorrhage, especially if Rh-negative mother | |||
**Consider: [[BMP]], [[LFTs]], [[Urinalysis|UA]], [[Uric Acid|uric acid]] if preeclampsia suspected | |||
*Fetal monitoring | |||
**No role for fetal heart rate monitoring once IUFD is confirmed | |||
==Management== | ==Management== | ||
*Hemodynamic stabilization | |||
**IV access, fluid resuscitation as needed | |||
**Transfuse blood products if evidence of hemorrhage or DIC | |||
*Rh immunoglobulin | |||
**Administer [[RhoGAM]] to all Rh-negative mothers | |||
**Standard dose (300 mcg) covers up to 30 mL of fetal whole blood | |||
**Additional doses guided by Kleihauer-Betke results | |||
*DIC management | |||
**If evidence of coagulopathy, correct with FFP, cryoprecipitate, and/or platelets as indicated | |||
**Target fibrinogen > 150–200 mg/dL | |||
*Delivery planning | |||
**Induction of labor is the standard approach for most patients | |||
**Timing is generally at the discretion of OB; urgent delivery is indicated if: | |||
***Active hemorrhage | |||
***DIC | |||
***Sepsis/chorioamnionitis | |||
***Preeclampsia with severe features | |||
**Methods of induction vary by gestational age (misoprostol, oxytocin, or mechanical dilation) | |||
**Cesarean delivery is rarely indicated and should be avoided if possible given increased maternal morbidity without fetal benefit | |||
*Supportive care | |||
**Emotional support is critical — grief counseling, social work involvement | |||
**Allow family time with the infant after delivery when desired | |||
**Pain management (including neuraxial analgesia for labor) | |||
==Disposition== | ==Disposition== | ||
*All patients with confirmed IUFD require admission and obstetric consultation | |||
*Transfer to a facility with OB capability if diagnosed at a facility without obstetric services | |||
*Urgent OB consultation if concurrent DIC, hemorrhage, sepsis, or preeclampsia | |||
*Social work and/or chaplaincy involvement should be arranged early | |||
*Postpartum considerations include: | |||
**Lactation suppression counseling | |||
**Grief support and follow-up | |||
**Autopsy and placental pathology (per patient preference) to determine etiology | |||
==See Also== | ==See Also== | ||
*[[Spontaneous abortion]] | |||
*[[Placental abruption]] | |||
*[[Preeclampsia]] | |||
*[[DIC]] | |||
*[[Third trimester bleeding]] | |||
*[[Chorioamnionitis]] | |||
==External Links== | ==External Links== | ||
*[https://www.acog.org/clinical/clinical-guidance/obstetric-care-consensus/articles/2020/03/management-of-stillbirth ACOG Obstetric Care Consensus: Management of Stillbirth] | |||
*[https://www.aafp.org/pubs/afp/issues/2007/1101/p1295.html AAFP: Evaluation of Fetal Death] | |||
==References== | ==References== | ||
Latest revision as of 09:35, 22 March 2026
Background
- Defined as fetal death after 20 WGA (weeks gestational age)
- Prior to 20 WGA, fetal loss is classified as spontaneous abortion
- Occurs in approximately 1 in 160 pregnancies
- Risk increases with advancing gestational age
- Most common causes include:
- Placental abnormalities (e.g. abruption, insufficiency) — most common identifiable cause
- Chromosomal/genetic abnormalities
- Maternal conditions (preeclampsia, diabetes in pregnancy, chronic hypertension, thrombophilias, autoimmune disease)
- Umbilical cord abnormalities (knots, prolapse, compression)
- Intrauterine infection (e.g. chorioamnionitis, CMV, parvovirus B19, syphilis, listeria)
- Fetal Hydrops
- Cause remains unexplained in up to 25–60% of cases
Clinical Features
- Decreased or absent fetal movement (most common presenting complaint)
- Vaginal bleeding (may or may not be present)
- Uterine cramping or contractions
- Absence of fetal heart tones on Doppler
- Loss of pregnancy symptoms (e.g. breast tenderness, nausea)
- Uterus may be small for gestational age
- If prolonged fetal demise (retained > 3–4 weeks):
- Signs/symptoms of DIC (bleeding, petechiae, ecchymosis)
Differential Diagnosis
Vaginal Bleeding in Pregnancy (>20wks)
- Emergent delivery
- Placental abruption
- Placenta previa
- Vasa previa
- Uterine rupture
- Preterm labor
- Vaginal trauma
- Placenta accreta
- Intrauterine fetal demise
Evaluation
- Ultrasound
- Absence of fetal cardiac activity on real-time ultrasound is diagnostic
- Should be confirmed by two experienced operators if any uncertainty
- Additional findings: overlapping skull bones (Spalding sign), soft tissue edema, echogenic amniotic fluid
- Labs
- CBC — evaluate for anemia, thrombocytopenia
- Coagulation studies (PT/INR, PTT, fibrinogen) — screen for DIC
- Risk of DIC increases significantly if fetus retained > 4 weeks
- Fibrinogen < 200 mg/dL is concerning for consumptive coagulopathy
- Type and screen (or crossmatch if actively bleeding)
- Kleihauer-Betke test — to quantify fetomaternal hemorrhage, especially if Rh-negative mother
- Consider: BMP, LFTs, UA, uric acid if preeclampsia suspected
- Fetal monitoring
- No role for fetal heart rate monitoring once IUFD is confirmed
Management
- Hemodynamic stabilization
- IV access, fluid resuscitation as needed
- Transfuse blood products if evidence of hemorrhage or DIC
- Rh immunoglobulin
- Administer RhoGAM to all Rh-negative mothers
- Standard dose (300 mcg) covers up to 30 mL of fetal whole blood
- Additional doses guided by Kleihauer-Betke results
- DIC management
- If evidence of coagulopathy, correct with FFP, cryoprecipitate, and/or platelets as indicated
- Target fibrinogen > 150–200 mg/dL
- Delivery planning
- Induction of labor is the standard approach for most patients
- Timing is generally at the discretion of OB; urgent delivery is indicated if:
- Active hemorrhage
- DIC
- Sepsis/chorioamnionitis
- Preeclampsia with severe features
- Methods of induction vary by gestational age (misoprostol, oxytocin, or mechanical dilation)
- Cesarean delivery is rarely indicated and should be avoided if possible given increased maternal morbidity without fetal benefit
- Supportive care
- Emotional support is critical — grief counseling, social work involvement
- Allow family time with the infant after delivery when desired
- Pain management (including neuraxial analgesia for labor)
Disposition
- All patients with confirmed IUFD require admission and obstetric consultation
- Transfer to a facility with OB capability if diagnosed at a facility without obstetric services
- Urgent OB consultation if concurrent DIC, hemorrhage, sepsis, or preeclampsia
- Social work and/or chaplaincy involvement should be arranged early
- Postpartum considerations include:
- Lactation suppression counseling
- Grief support and follow-up
- Autopsy and placental pathology (per patient preference) to determine etiology
