What is the appropriate emergency department workup for a 24‑week pregnant woman presenting with a near‑syncope episode?

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Emergency Department Workup for Near-Syncope in a 24-Week Pregnant Woman

The ED workup for a 24-week pregnant woman with near-syncope should prioritize immediate positioning in left lateral decubitus, followed by a mandatory 12-lead ECG, orthostatic vital signs, and at least 4 hours of continuous fetal heart rate monitoring, with disposition determined by the presence or absence of high-risk cardiac features. 1, 2, 3

Immediate Management Upon Arrival

  • Position the patient in left lateral decubitus immediately to relieve aortocaval compression from the gravid uterus, which is a pregnancy-specific cause of presyncope at 24 weeks gestation 1
  • If left lateral positioning is not feasible, assist the patient to sit or lie down in any safe position within 1-2 minutes of arrival 1
  • Administer supplemental oxygen to maintain maternal oxygen saturation >95% to ensure adequate fetal oxygenation 3
  • Establish two large-bore (14-16 gauge) intravenous lines above the level of the diaphragm 3, 4

Risk Stratification and Activation Criteria

Activate emergency cardiology consultation immediately if any of the following high-risk features are present: 1, 2

  • No improvement within 1-2 minutes of positioning or symptoms worsen 1
  • Near-syncope occurred during exertion (suggests cardiac etiology) 2
  • Palpitations preceding the episode 1
  • History of structural heart disease or heart failure 1, 2
  • Family history of sudden cardiac death 1, 2
  • Symptoms suggesting myocardial infarction or stroke 1

Mandatory Diagnostic Testing

12-Lead ECG (Required for All Patients)

  • Obtain a 12-lead ECG immediately as it is noninvasive, inexpensive, and can identify life-threatening conditions despite a low 5% overall yield 1, 2
  • Specifically evaluate for: myocardial infarction or ischemia, arrhythmias or conduction abnormalities, prolonged QT interval, ventricular hypertrophy, and pre-excitation patterns 2

Orthostatic Vital Signs

  • Measure blood pressure and heart rate in supine position, then after standing 1, 2
  • Abnormal results are defined as: systolic BP drop >20 mmHg or heart rate increase >20 bpm 1, 2

Laboratory Testing

  • Obtain routine blood work including a coagulation panel with fibrinogen level 3
  • Serum fibrinogen <200 mg/dL is an adverse factor requiring extended monitoring 3

Fetal Assessment (Mandatory at 24 Weeks)

  • Initiate continuous electronic fetal heart rate monitoring for at least 4 hours minimum 3, 4
  • Perform fetal heart rate auscultation as soon as maternal stabilization is achieved 3
  • Obtain urgent obstetrical ultrasound if gestational age is uncertain or if delivery may be anticipated 3

Disposition Algorithm

Safe for Discharge Criteria (All Must Be Present)

  • No structural heart disease 1, 2
  • Normal 12-lead ECG 1, 2
  • Clinical features clearly suggesting vasovagal or orthostatic syncope 1, 2
  • No high-risk features present 1
  • Normal fetal heart rate monitoring for 4 hours 3
  • No uterine tenderness, significant abdominal pain, or vaginal bleeding 3

Admission Criteria (Any One Present)

Admit for 24-hour observation if any of the following are present: 1, 2, 3

  • Age >45 years 2
  • History of congestive heart failure or ventricular arrhythmias 2
  • Abnormal ECG 2
  • Physical exam findings of heart failure 2
  • Cardiac murmur suggesting outflow obstruction 2
  • Uterine tenderness or significant abdominal pain 3
  • Vaginal bleeding 3
  • Sustained contractions (>1 per 10 minutes) 3
  • Rupture of membranes 3
  • Atypical or abnormal fetal heart rate pattern 3
  • Serum fibrinogen <200 mg/dL 3

Additional Considerations

Pregnancy-Specific Etiologies to Consider

  • Supine hypotensive syndrome (managed by left lateral positioning) 1
  • Physiologic changes including increased cardiac output, decreased systemic vascular resistance, and aortocaval compression 2
  • Common benign causes: vasovagal syncope and orthostatic hypotension 2
  • Life-threatening causes to exclude: pulmonary embolism, cardiac arrhythmias, amniotic fluid embolism 2

Imaging Studies

  • Do not defer or delay radiographic studies (including abdominal CT) if indicated for maternal evaluation due to concerns about fetal radiation exposure 3
  • Focused abdominal sonography for trauma (FAST) should be considered if intraperitoneal bleeding is suspected 3

Rh Status Management

  • Administer anti-D immunoglobulin to all Rh-negative pregnant trauma patients 3
  • Perform Kleihauer-Betke testing in Rh-negative patients to quantify maternal-fetal hemorrhage and determine need for additional anti-D doses 3

Critical Pitfalls to Avoid

  • Do not assume benign vasovagal syncope without obtaining a 12-lead ECG 1, 2
  • Do not discharge patients with any high-risk features, even if symptoms have resolved 1, 2
  • Do not delay fetal monitoring in viable pregnancies (≥23 weeks) 3
  • Patients with 3-4 risk factors have a 57.6-80.4% risk of 1-year mortality or significant arrhythmia, while those with zero risk factors have 0% 72-hour cardiac mortality 2

Continuous Monitoring

  • Continuous cardiac monitoring is appropriate for the first 24 hours if arrhythmia is suspected 2
  • Arrange outpatient cardiology follow-up if any concerning features are present 2

References

Guideline

Management of Near Syncope (Presyncope) in Pregnancy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Evaluation and Management of Syncope in Pregnancy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Guidelines for the Management of a Pregnant Trauma Patient.

Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC, 2015

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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