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Learn Mat 6
Learn Mat 6
Learn Mat 6
TOPIC I. Care of At-Risk/ High Risk: Nursing Care of the Client during Labor and Delivery – FHR and
FHT monitoring
Let’s first review your background of anatomy and physiology of reproductive system.
Introduction
Nursing procedures performed during labor and delivery includes monitoring of the FHR, monitoring uterine activity and
cervical examination.
Analysis of the FHR is one of the primary evaluation tools used to determine fetal oxygen status indirectly. FHR
assessment can be done intermittently using a fetoscope (a modified stethoscope attached to a headpiece) or a
Doppler (ultrasound) device, or continuously with an electronic fetal monitor applied externally or internally.
Fetal Monitoring
• The fetal monitor displays the fetal heart rate (FHR).
• The device monitors uterine activity.
• The monitor assesses frequency, duration, and intensity of contractions.
• The monitor assesses FHR in relation to maternal contractions.
• Baseline FHR is measured between contractions; the normal FHR at term is 110 to 160 beats/minute.
Interpretation of FHR and uterine contractions should be conducted at regular intervals. The Association of Women’s
Health, Obstetric, and Neonatal Nurses (AWHONN) specifies guidelines for monitoring patients who lack risk factors and
monitoring of patients who have risk factors.
• the FHR and uterine activity should be assessed every 30 minutes during the first stage of labor and every 15
minutes during the second stage of labor.
• The assessment of the FHR may be done via auscultation or electronically, and the assessment of uterine activity
may be done via palpation or electronically.
• AWHONN guidelines specify that a patient with risk factors needs continuous FHR monitoring, and the
assessment should be done every 15 minutes during the first stage of labor and every 5 minutes during the
second stage of labor.
• Risk factors are those known items which could cause complications to either the mother or the fetus/neonate.
• Risk factors can be discovered at any stage of pregnancy or during the labor process.
• Risk factors can be found to originate in the patient’s obstetric (OB) history, medical history, current OB status,
or psychosocial status. Examples of each include:
Intermittent FHR monitoring is the periodic auscultation of FHR by either fetoscope or a handheld Doppler device.
Because the Doppler is more sensitive to fluctuations in FHR, it’s more commonly used.
Up and about
Intermittent FHR monitoring allows the patient to ambulate during the first stage of labor. Because auscultation isn’t
done until after a contraction, this type of monitoring doesn’t document how the fetus is responding to the stress of
labor as well as continuous FHR monitoring does.
Limited Intermittent
FHR monitoring can detect FHR baseline rate and rhythm as well as changes from the baseline; however, it can’t detect
variability in FHR as documented by electronic fetal monitoring.
Baseline
Risky business
For patients whose pregnancy is considered high-risk—because of an increased risk for prenatal death, cerebral palsy or
neonatal encephalopathy, and the use of oxygen for labor induction or augmentation—continuous electronic fetal
monitoring is recommended.
External uterine palpation can tell you the frequency, duration, and intensity of contractions and the relaxation time
between them. The character of contractions varies with the stage of labor and the body’s response to labor-inducing
drugs, if administered. As labor advances, contractions become more intense, occur more often, and last longer. In some
patients, labor progresses rapidly, preventing the patient from entering a health care facility.
• Review the patient’s admission history to determine the onset, frequency, duration, and intensity of
contractions. Also, note where contractions feel strongest or exert the most pressure.
• Describe the procedure to the patient.
• Assist the patient into a comfortable side-lying position.
• Drape the patient with a sheet.
• Place the palmar surface of your fingers on the uterine fundus and palpate lightly to assess contractions.
Each contraction has three phases: increment (rising), acme (peak), and decrement (letting down or ebbing).
How fast?
To assess frequency, time the interval between the beginning of one contraction and the beginning of the next.
How long?
To assess duration, time the period from when the uterus begins tightening or contracting until it has relaxed
completely.
How hard?
To assess intensity, palpate the uterine fundus and compare the degree of tightness as described previously in
the section, “Do you feel a nose (mild contraction), a chin (moderate contraction), or a forehead (strong contraction)?”
• Determine how the patient copes with discomfort by assessing her breathing and relaxation techniques.
• Assess contractions in low-risk patients every 30 minutes in the latent phase and the active phases, and every 15
minutes in the transition phase of the first stage of labor. More frequent assessments are required for high-risk
patients. High-risk fetal status assessments should also occur every 30 minutes during the latent phase, every 15
minutes during the active phase, and every 5 minutes in the second stage.
Contraction without relaxation
If any contraction lasts longer than 90 seconds and isn’t followed by uterine muscle relaxation, or if the relaxation period
is less than 1 minute between contractions, notify the doctor. This may indicate tachysystole of the uterus or tetanic
contractions. When the uterus doesn’t relax, or the relaxation period is less than 1 minute, uteroplacental blood flow is
interrupted, which can lead to fetal hypoxia and fetal distress. If you determine that the patient’s contractions last
longer than 90 seconds or if the relaxation period is less than 1 minute, follow these steps:
• Discontinue the oxytocin infusion to stop uterine stimulations (if the patient is receiving oxytocin).
• Make sure that the patient is lying on her left side; this increases uteroplacental perfusion.
• Administer oxygen via face mask to increase fetal oxygenation.
• Notify the doctor or nurse-midwife immediately.
Continuous external electronic monitoring is an indirect, noninvasive procedure. Two devices, an ultrasound transducer
and a tocotransducer, are placed on the mother’s abdomen to evaluate fetal well-being and uterine contractions during
labor. These devices are held in place with an elastic stockinette or by using plastic or soft straps.
Steps to follow:
• Explain the procedure to the patient, and make sure that she has signed a consent form, if required by your
facility.
• Ensure that the patient you are caring for is the same patient you are documenting on, whether you are
documenting on a paper chart or electronically. Make sure your documentation and the strip (whether a paper
strip or an electronic one) match for all components of the FHR assessment.
Fetal strip evaluation should be done in systematic fashion that addresses all components of the strip. In 2008, the
National Institute of Child Health and Human Development (NICHD) has updated criteria for interpretation of electronic
FHR monitoring data that is considered the national standard of assessment and documentation of electronic FHR
monitoring data. The strip should be evaluated considering uterine activity/contractions, the baseline FHR, the
variability of the FHR, periodic or episodic changes to the FHR, and changes in the FHR over time. Following the
evaluation of the electronic FHR monitoring strip, the strip should be graded into one of three categories.
Uterine activity
Uterine contraction activity should be evaluated in segments of 10 minutes but averaged over a 30-minute window. A
normal contraction pattern should mean that there are less than or equal to five contractions in 10 minutes (averaged
over 30 minutes). If greater than five contractions occur in the 10-minute period, the terminology assigned to it is
tachysystole. Additional components of a uterine contraction pattern assessment include intensity of the contraction,
duration of the contraction, and rest or relaxation time between contractions. Uterine tachysystole or hypercontractility
are not considered valid term to apply to assessment of uterine activity. Also, the assessment of the uterine activity
should be considered in light of the response of the FHR.
• The normal baseline FHR should range from 110 to 160 beats per minute (bpm) and is rounded to increments of
5 bpm in a 10-minute window.
• Periodic and episodic changes are not considered when determining the baseline.
• An FHR in excess of 160 bpm is defined as fetal tachycardia and an FHR less than 110 bpm is defined as fetal
bradycardia.
• Sinusoidal pattern is a smooth undulating wave pattern in which no acceleration or deceleration are noted. (See
Identifying baseline FHR irregularities, page 337.)
FHR variability is a fluctuation of the baseline FHR that occur as variations in the amplitude and frequency. This
fluctuation represents the interaction between the sympathetic and parasympathetic nervous systems of the fetus. The
constant interactions between these systems results in a moment-to-moment change in the FHR. It signals that both
nervous systems are working. This interaction can be termed as: absent, minimal, moderate, or marked and is
determined by the bpm.
Changes to the FHR can be reassuring or non-reassuring, depending on the change and the whole picture of FHR and
uterine activity and last less than 2 minutes. (See Changes to the FHR, pages 338 and 339.) Changes that last greater
than 2 minutes and less than 10 minutes are considered a prolonged change, and changes that last more than 10
minutes are considered a baseline change.
Episodic or periodic
Changes to the FHR are classified as either episodic or periodic. Episodic changes are not associated with uterine
contractions, and periodic changes are associated with uterine contractions.
• the fetal monitor strip records the FHR in beats per minute in the top recording and
• uterine activity (UA) in millimeters of mercury (mm Hg) in the bottom recording.
You can obtain information on fetal status and labor progress by reading the strips horizontally and vertically.
• Reading horizontally on the FHR or the UA strip, each small block represents 10 seconds. Six consecutive small
blocks, separated by a dark vertical line, represent 1 minute.
• Reading vertically on the FHR strip, each block represents an amplitude of 10 beats/minute. Reading vertically
on the UA strip, each block represents 5 mm Hg of pressure.
2 readings, 1 printout
Classifications of FHR monitoring were developed, by the National Institute of Child Health and Human
Development (NICHD), as a means to help organize the data obtained from a systematic evaluation of the FHR. There
are three categories of interpretation: Class I, Class II, and Class III.
Class I (Normal)
• The tracings are normal and a solid predictor of a normal fetal acid-base balance.
• No actions are recommended for tracings in this class.
• Criteria for this class includes:
➢ baseline FHR within normal limits (110 to 160),
➢ moderate variability,
➢ no late or variable decelerations, and early deceleration and
➢ acceleration may or may not be present.
Class II (Indeterminate)
• The tracings are considered abnormal and are predictive of an abnormal fetal acid-base balance.
• Efforts to resolve the FHR pattern needs to be made.
• Criteria for this class includes:
➢ absent FHR variability with recurrent late decelerations,
➢ recurrent variable deceleration or bradycardia, or sinusoidal pattern.
Cardiotocography (CTG)
• a technical means of recording (-graphy), the fetal heart beat (-cardio), and the uterine contractions (-toco)
during pregnancy, typically in the third trimester.
• a test used in pregnancy to monitor both the fetal heart pattern as well as the uterine contractions.
• It should only use in the 3rd trimester when fetal neural reflexes are present.
• Its purpose is to monitor fetal well-being & allows early detection of fetal distress antenatal or intra-partum.
• An abnormal CTG indicates the need for further invasive investigation & ultimately may lead to emergency CS.
Continuous external electronic monitoring is an indirect, noninvasive procedure. Two devices, an ultrasound
transducer and a tocotransducer, are placed on the mother’s abdomen to evaluate fetal well-being and uterine
contractions during labor. These devices are held in place with an elastic stockinette or by using plastic or soft straps.
Internal monitoring, also called direct monitoring, is an invasive procedure that uses a spiral electrode attached
to the presenting fetal part (usually the scalp) and an IUPC. This helps assess fetal response to uterine contractions,
measures intrauterine pressure, and tracks labor progress.
Internal monitoring is indicated for high-risk pregnancies. However, it can be performed only if the amniotic sac
has ruptured, the cervix is dilated at least 2 cm, and the presenting part of the fetus is at least in the 1 station. Maternal
complications of internal fetal monitoring may include uterine perforation and intrauterine infections. Fetal
complications may include abscess, hematoma, and infection.
Spiral electrode
The spiral electrode, sometimes called a fetal scalp electrode or FSE, detects the fetal heartbeat and transmits it to the
monitor, which converts the signals to a fetal electrocardiogram (ECG) waveform.
An IUPC may be used if external uterine monitoring doesn’t provide satisfactory information. It may also be necessary in
high-risk pregnancies or if the patient is obese. Insertion of an IUPC is done only by specially trained health care
provider. Nurses need to check the policy per institution on who is allowed to place an IUPC.
References:
1. Pilliteri, Adele, (2010). Maternal and child Health Nursing: Care of the Childbearing and Child Rearing Family (6th
ed). Philadelphia: Lippincott Williams and Wilkins.
2. https://www.youtube.com/watch?v=BCVOjdX4mso
3. https://www.youtube.com/watch?v=DvcDXvlCXAE
4. https://www.youtube.com/watch?v=fDeulZdDc_g
5. https://www.youtube.com/watch?v=ac14n5uD4_0&t=21s