Fetal Tachycardia in Labor: Definition and Management
Fetal tachycardia in labor is defined as a baseline fetal heart rate greater than 160 beats per minute, and the initial management focuses on identifying and treating the underlying cause—most commonly chorioamnionitis or maternal fever—while implementing intrauterine resuscitative measures. 1, 2
Definition and Recognition
- Fetal tachycardia is defined as a baseline heart rate exceeding 160 bpm on continuous electronic fetal monitoring, assessed over a 10-minute window. 1
- The baseline rate must be sustained and distinguished from transient accelerations or maternal heart rate. 1
- Tachycardia is classified as part of the "BRA" (Baseline Rate Assessment) component of the DR C BRAVADO mnemonic for fetal heart rate interpretation. 1
Primary Causes to Identify
The most critical step is determining the etiology, as this drives management:
- Chorioamnionitis or intrauterine infection is the most common cause of fetal tachycardia after membrane rupture, as bacteria can ascend more easily once membranes are ruptured. 2, 3
- Maternal fever from any source (infection being most concerning) directly causes fetal tachycardia. 2, 4
- Early fetal compensatory response to hypoxia can manifest as tachycardia before other concerning signs develop. 2
- Fetal tachycardia combined with meconium-stained amniotic fluid increases the relative risk of fetal infection 51-fold, suggesting the fetus itself is infected rather than just the membranes. 3
Initial Management Steps
Immediate Assessment
- Assess maternal temperature and vital signs immediately to identify fever or signs of infection as the underlying cause. 2
- Evaluate the complete fetal heart rate tracing for baseline variability, accelerations, and decelerations—tachycardia with preserved moderate variability and accelerations is far less concerning than tachycardia with minimal/absent variability. 1
- Perform or review recent vaginal examination to assess cervical dilation, station, and rule out rapid labor progression. 2
Intrauterine Resuscitative Measures
Implement general resuscitative interventions while investigating the cause:
- Change maternal position to left lateral to optimize uteroplacental blood flow and relieve potential cord compression. 2, 5
- Administer oxygen at 6-10 L/min via face mask to maximize maternal and fetal oxygenation. 2, 5
- Give IV fluid bolus to improve maternal intravascular volume and uteroplacental perfusion. 2, 5
- Discontinue oxytocin if being administered, as uterine tachysystole can contribute to fetal stress. 2, 5
Infection-Specific Management
If chorioamnionitis is suspected based on maternal fever, fetal tachycardia, uterine tenderness, or foul-smelling amniotic fluid:
- Administer broad-spectrum antibiotics immediately without waiting for culture results. 2
- Switch to continuous electronic fetal monitoring if using intermittent auscultation, as chorioamnionitis necessitates continuous monitoring. 1
- Recognize that fetal tachycardia may be an early indicator of intrauterine infection, often preceding maternal fever. 4
Monitoring Strategy
- Continuous electronic fetal monitoring is mandatory once tachycardia is identified to assess for development of concerning patterns (late decelerations, loss of variability). 2
- Consider internal fetal scalp electrode placement if external monitoring provides inadequate signal quality for accurate heart rate and variability assessment. 2
- Assess the overall clinical picture using the "stoplight algorithm" or NICHD categorization system to determine if the tracing is Category I (reassuring), II (indeterminate), or III (abnormal). 1
Critical Pitfalls to Avoid
- Do not dismiss isolated fetal tachycardia as benign—it warrants investigation for infection even in the absence of maternal fever, as fetal tachycardia can precede maternal temperature elevation by hours. 4
- Do not confuse fetal tachyarrhythmias (sustained heart rates >180 bpm from primary cardiac rhythm disturbances) with labor-related tachycardia—true fetal arrhythmias require specialized fetal cardiology evaluation and may need antiarrhythmic therapy. 6, 7, 8
- Meconium-stained fluid with tachycardia should raise high suspicion for fetal infection rather than being automatically attributed to acute fetal distress from hypoxia. 3
- Loss of baseline variability accompanying tachycardia significantly increases concern for fetal acidosis and may indicate progression to Category III tracing requiring expedited delivery. 1, 9
When to Expedite Delivery
- If tachycardia is accompanied by absent baseline variability with recurrent late or prolonged decelerations (Category III tracing), expedited delivery via operative vaginal delivery or cesarean section is indicated. 5, 9
- If intrauterine resuscitation and treatment of underlying infection do not improve the tracing, delivery should be expedited based on the overall clinical assessment. 5, 9