Intrapartum Fetal Surveillance Flashcards

1
Q

What are some indications for Electronic Fetal Monitoring?

A

Any High risk condition:

  1. maternal medical conditions: DM, HTN, etc
  2. Maternal obstetric complications: hx of prior c-sections, 42+ weeks, preeclampsia, gestational DM
  3. intrapartum complications
  4. epidural use
  5. known or suspected fetal conditions
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2
Q

What functions do each of the two transducers perform with electronic fetal monitoring?

A
  1. uterine contractions

2. fetal heart rate

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3
Q

If you use structured intermittent auscultation, how often should you listen?

A

every 15-30 minutes in active first stage of labor and every 5-15 minutes in second stage of labor

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4
Q

What pnemonic describes interpreting continuous electronic fetal monitoring?

A

DR C BRAVADO

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5
Q

What does DR C BRAVADO stand for?

A
Determine Risk
Contractions
Baseline RAte
Accelerations
Decelerations
Overall Assessment
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6
Q

What are 3 ways to monitor contractions?

A
  1. palpation
  2. external transducer
  3. intrauterine pressure catheter
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7
Q

What is considered a normal number of contractions?

A

= 5 contractions in 10 minutes averaged over 30 minutes

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8
Q

What is considered tachysystole with regards to contractions?

A

> 5 contractions in 10 minutes averaged over 30 minutes

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9
Q

How is the Baseline RAte defined?

A

Mean fetal heart rate rounded to increments of 5 BPM during a 10-minute segment

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10
Q

How is baseline bradycardia defined?

A

Baseline <110 BPM for greater than 10 minutes

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11
Q

What are 7 maternal causes of baseline bradycardia?

A
  1. supine positioning
  2. hypotension
  3. connective tissue disease, ie lupus
  4. hypothermia
  5. hypoglycemia
  6. excessive vagal stimulation
  7. tachysystole
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12
Q

What are 4 fetal causes of Baseline Bradycardia?

A
  1. prolonged cord occlusion/cord prolapse
  2. fetal hypoxia
  3. cardiac conduction or anatomic defects
  4. Post dates >42 0/7 weeks
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13
Q

How is baseline Tachycardia defined?

A

Baseline >160 BPM for greater than 10 minutes

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14
Q

How is variability defined?

A

Fluctuations in baseline FHR that are irregular in amplitude and frequency

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15
Q

What are the 4 ways variability can be characterized?

A
  1. absent: undetectable
  2. minimal: AMPLITUDE range detectable but = 5 BPM
  3. Moderate: 6 to 25 BPM
  4. Marked: >25 BPM
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16
Q

What are 6 maternal causes of Decreased Variability?

A
  1. fever
  2. CNS depressants (ie opioids, benzos, MgSO4)
  3. general anesthesia
  4. Alcohol
  5. Corticosteroids
  6. Anticholinergics/parasympathetics
17
Q

What are 6 fetal causes of decreased variability?

A
  1. fetal sleep cycles (20- to 40-minute duration)
  2. prematurity
  3. cardiac anomalies
  4. fetal tachycardia
  5. hypoxia/acidosis
  6. CNS anomalies
18
Q

How are accelerations defined?

A

visually apparent, abrupt increase in FHR above baseline
- onset to peak in <30 seconds

Peak must be >/= 15 BPM above baseline
(or =10 sec if <32 weeks gestation)

Must last >/=15 seconds
(or >/=10 seconds if <32 weeks gestation)

Must return to baseline within 2 minutes

19
Q

What are the 3 classifications of Decelerations?

A
  1. Early
  2. Variable
  3. Late
20
Q

How are decelerations defined?

A

by their rate of onset (abrupt or gradual) and their timing in relation to the contraction

21
Q

How are early decelerations defined?

A

visually apparent, gradual decrease in FHR with return to baseline in association with a uterine contraction

  • nadir coincides with the peak of contraction
  • onset to nadir >/= 30 seconds (gradual in onset)
22
Q

What is the physiology of early decelerations?

A

Fetal head compression –> local changes in cerebral blood flow –> stimulation of vagal centers in the fetus –> decelerations of FHR

23
Q

How are variable decelerations defined?

A

visually apparent, abrupt decrease in FHR below baseline

  • onset to nadir <30 seconds
  • decrease in FHR is >/= 15 BPM, with duration of >/=15 seconds (but less than 2 minutes)
24
Q

What is the physiology behind variable decelerations?

A

cord compression
–> rise in fetal peripheral resistance –> sudden fetal HTN –> parasympathetic outflow –> slowing of fetal atrial pacemaker –> variable FHR deceleration

25
When are decelerations described as recurrent?
if decelerations occur with >/= 50% of contractions in any 20 minute period
26
What is the purpose of an amnioinfusion?
1. reduces cord compression 2. reduces variable decelerations leads to fewer cesarean deliveries use with recurrent variable decelerations not useful for late decelerations or meconium
27
When performing amnioinfusion, what volumes of fluids are used?
initial infusion of 250-500 mL maintenance rate of 50-60 mL/hour
28
How are late decelerations defined?
onset to nadir >/=30 seconds with nadir occurring AFTER peak of contraction Generally, onset, nadir, and recovery of the deceleration occur after the start, peak, and ending contraction, respectively
29
Describe the physiology of a late deceleration
uteroplacental insufficiency --> fetal hypoxemia --> O2 centralized via peripheral vasoconstriction --> hypertension --> late FHR deceleration
30
What is a prolonged deceleration?
Any deceleration that is at least 15 BPM below the baseline that lasts >/= 2 minutes, but <10 minutes
31
What is the etiology of a sinusoidal pattern of FHR? (list 3)
1. fetal anemia 2. evolving asphyxia 3. may represent a terminal pattern
32
Describe the risk of fetal acidemia based of NICHD Categories.
Category I - No risk Category II - Indeterminate risk (insufficient research) Category III - High risk (Abnormal)
33
Describe a Category III FHR tracing.
``` - sinusoidal pattern OR - absent FHR variability with any of the following: > recurrent late decelerations > recurrent variable decelerations > bradycardia ```
34
Describe a Category I FHR Tracing.
Must have all of the following: - baseline 110 to 160 BPM - moderate baseline variability - late or variable decelerations absent - accelerations present or absent