MENNONITE COLLEGE OF NURSING at Illinois State University Maternal Infant Nursing -316 Fetal Assessment Worksheet The purpose of this worksheet is to guide your understanding of the normal fetal heart rate patterns, variations in heart rate patterns during labor, components of the biophysical profile, tests of fetal maturity, and antenatal testing interpretation. Complete the worksheet and bring it to class on the assigned day. We will review and discuss the content in the worksheet in class. You will be responsible for this material and will be tested on it. Chapter 21 on Assessment of Fetal Well-being and section on Evaluating Labor Progress & Electronic Fetal Monitoring in Chapter 23 in Olds(9th ed.) to complete most of the questions in this worksheet. The next two pages of this worksheet and the last several slides on the Fetal Assessment Powerpoint have current information on fetal monitoring interpretation that would be extremely helpful to you when you are assigned to be in Labor for a clinical day. It would behoove you to bring it with you to clinical on those days. 1 FETAL HEART RATE/VARIABILITY/DECELERATIONS I. Fetal Heart Rate (FHR) A. Baseline FHR consists of: 1. The mean of the FHR observed between contractions during a continuous 10minute period of monitoring rounded to the nearest 5bpm. It does not include the rate during accelerations or decelerations. Fetal Heart Rate levels: Marked bradycardia 70 BPM Mod. bradycardia 71-99 BPM Mild bradycardia 100-109 BPM Normal 110-160 BPM Moderate tachycardia 161-179 BPM Marked tachycardia >180 BPM • 2. FHR variability-- Baseline variability is a measure of the interplay effect between the sympathetic nervous system and the parasympathetic nervous system. It is defined as: • • Fluctuations in the FHR of two cycles per min or greater Variability is visually quantitated as the amplitude of peak-to-trough in bpm-Absent—amplitude range undetectable-Minimal—amplitude range detectable but 5 bpm or fewer-Moderate (normal)—amplitude range 6-25 bpm-Marked—amplitude range greater than 25 bpm **Beat-to-beat Variability is probably the most accurate indicator of fetal well-being that the nurse has. If BTBV is poor, the fetus is probably in distress and needs to be delivered SOON. • • • • B. Periodic changes - changes in FHR, either accelerations or decelerations, from baseline returning to baseline that occur in response to contractions or fetal movement 1. Accelerations 1. Description-- A visually apparent abrupt increase (onset to peak less than 30 sec.) in the FHR from the most recently calculated baseline The duration of an acceleration is defined as the time from the initial change in FHR from baseline to the return of the FHR to baseline At 32 weeks of gestation and beyond, an acceleration has an acme of 15 bpm or more above baseline, with a duration of 15 sec. or more but less than 2 min. Before 32 weeks gestation an acceleration has an acme of 10 bpm or more above baseline, with a duration of 10 sec. or more but less than 2 min. If an acceleration lasts 10 min. or longer it is a baseline change 2. Cause- stimulation of autonomic nervous system of the fetus seen with fetal movement, vaginal exams, abdominal palpation, uterine contractions. These are usually seen as signs of fetal well-being. 3. Nursing intervention - None. 2 2. Decelerations-- Periodic decreases in FHR from the normal baseline. There are 3 types that we discuss. A. Early Decelerations 1. Description-- "mirrors" contraction. In association with a uterine contraction, a visually apparent, gradual (onset to nadir 30 sec. or more) decrease in FHR with return to baseline. *Nadir of the deceleration occurs at the same time as the peak of the contraction 2. Cause - head compression after: - Uterine contraction - Vaginal exam - Fundal pressure - Placing internal fetal scalp electrode 3. Nursing interventions--benign pattern, no intervention required. B. Late Decelerations 1. Description - In association with a uterine contraction, a visually apparent, gradual (onset to nadir 30 sec. or more) decrease in FHR with return to baseline. Onset, nadir, and recovery of the deceleration occur after the beginning, peak, and end of the contraction, respectively - Very ominous when associated with loss of STV, rising baseline, or tachycardia - Repetitious 2. Cause - uteroplacental insufficiency or decreased maternal-fetal exchange during contractions causing hypoxemia Seen with - Hyperstimulation of uterus with oxytocin - Toxemia - Postmaturity - SGA - Maternal diabetes, anemia, or cardiac disease - Placenta previa or abruption 3. Nursing interventions - Change maternal position to left lateral - Stop Pitocin/Oxytocin if being used - O2/mask at 7-10L/min - Correct maternal hypotension - Increase mainline IV rate (Bolus) - Elevate legs C. Variable Decelerations 1. Description-- V, U, or W shaped An abrupt (onset to nadir less than 30 sec), visually apparent decrease in the FHR below the baseline. The decrease in FHR is 15 bpm or more, with a duration of 15 seconds or more, but < 2 minutes. 2. 3. 3 Cause - umbilical cord compression. If repetitive, it may indicate nuchal cord (cord around baby’s neck). Nursing Intervention - Change maternal position - If severe, may need to try Amnioinfusion ASSESSMENT OF FETAL WELL-BEING Chapters 21 MATERNAL ASSESSMENT OF FETAL MOVEMENT 1. Describe the “Cardiff Count-to-10 Method” or “Daily Fetal Movement Record” (DFMR) method for assessing fetal movement. (sample instructions and chart in Self-Care Guide in back of text). Also see pp383-385. USE OF ULTRASONOGRAPHY IN PREGNANCY 2. Identify and define the 3 levels of ultrasound presently defined by American College of Obstetricians and Gynecologists (ACOG). a. b. c. 3. Name two methods that can be used when performing an ultrasound. Differentiate them. Which can be used earliest in pregnancy? a. b. 4. What information can be obtained from an ultrasound during the first trimester? second? Third? 5. Describe the measurements that can be obtained to determine gestational age of the fetus during the pregnancy. a. b. c. d. 6. How is ultrasound used to assess placental maturity (grading 0 – 3)? Placental location? Cervical length? 7. 4 Define IUGR and discuss the importance of early detection in relation to fetal well-being. ANTENATAL FETAL SURVEILLANCE 8. Why is Amniotic Fluid Volume (AFV) or Amniotic Fluid Index (AFI) evaluation important in assessing fetal wellbeing? 9. Review Tables 21-5 & 6 Biophysical Profile (BPP) (p.515) and become familiar with the 5 parameters assessed. Think about what two pieces of equipment are used to complete a BPP. What are the 2 most important components of the BPP? Nuchal Translucency Pg. 503. 10. Define Nuchal Translucency? 11. What does it detect? 12. At what gestation is it done? OTHER ANTENATAL TESTING 1. Complete the table on the next page on CST, and NST. 2. How is the vibroacoustic stimulator used in an NST? 5 ANTEPARTAL FETAL HEART RATE MONITORING Compare/contrast the NonStress Test (NST) & the Contraction Stress Test(CST) by completing the following table. Nonstress Test (NST) also called Fetal Activity Determination Test Contraction Stress Test (CST) Advantagest Disadvantages Procedure Interpretation of Tests: What terms are used? Include criteria used: Normal Reactive Clinical Significance Negative Clinical Significance Abnormal Nonreactive Clinical Significance Positive Clinical Significance Equivocal Unsatisfactory Clinical Significance Suspicious Hyperstimulation Unsatisfactory Risks to mother & fetus 6 Clinical Significance AMNIOTIC FLUID STUDIES 10. Contrast how amniocentesis is used early in pregnancy versus later in pregnancy. 11. What is the significance of the following amniotic fluid studies? a. AFP Screening-Maternal Serum Alpha Fetal Protein (MSAFP) is a screening tool for which defects in pregnancy? When is the test most accurate? What follow-up testing should be done if an abnormal result is obtained? b. Quadruple Check—what are the 4 tests included here? What do they detect? c. Bilirubin OD450/nm - normal value = (ch. 20 pp. 478-479) d. L/S Ratio e. Phosphatidylglycerol (PG) f. Color OTHER DIAGNOSTIC TESTS 12. What is Chorionic Villi Sampling and when is Chorionic Villi Sampling (CVS) done during a pregnancy? Why might this be advantageous to the mother? 13. Fetoscopy is not done as often as in the past because of advances in Sonography and use of PUBS. When might Fetoscopy still be indicated, and what is the nurse’s role during and after the procedure? 14. What is Cordocentesis/Percutaneous Umbilical Blood Sampling (PUBS) and how is it used during the 2nd and 3rd trimesters to detect fetal status? 15. What is the significance of fetal fibronectin in relation to preterm delivery? 7 INTRAPARTUM FETAL MONITORING AND CARE CHAPTER 23, BASIS FOR MONITORING 1. What are the goals of Fetal Heart Monitoring (FHM)? 2. Describe the advantages and disadvantages of external uterine monitoring. EVALUATION OF UTERINE ACTIVITY 3. In addition to uterine activity, what other activities of the mother may be reflected on the tracing with the tocodynamometer? 4. Internal monitoring measures what aspect of the uterine contraction that the external monitor does not measure? 5. Differentiate between the water-filled intrauterine pressure catheter (IUPC) from the INTRAN IUPC. Normal baseline uterine resting tone from an IUPC should remain between _5-15_ mm Hg. Normal pressures during uterine contractions should be 50-85 mm Hg. 6. Hypertonicity of the uterus puts a fetus at risk. How can the nurse detect the effects of hypertonicity on the fetus? What is the nursing action in this situation? (A Critical Thinking Exercise!) FYI: *If uterine pressure is > 30 mm Hg, there is oxygen getting to baby, but baby usually can compensate. *If uterine pressure is > 70 mm Hg, there is no perfusion of oxygen getting to the baby. The nurse needs to monitor closely to see that the fetus is able to cope with the oxygen supply. 7. Define the following: a. Duration of contraction b. Frequency of contraction (Review deceleration patterns discussed at beginning of worksheet.) 8. What changes in FHR pattern might you see indicating that the fetus is not coping? 8 9. Complete the following table on frequency of fetal monitoring. Low-Risk High-Risk Frequency of Auscultation Pregnancy Pregnancy 1st Stage Latent Phase Active Phase 2nd Stage EVALUATION OF FETAL HEART RATE Match the following terms and/or fetal heart rates: 1. 2. 3. 4. 5. 6. 7. 8. ____ ____ ____ ____ ____ ____ ____ ____ 9. ____ 10. ____ 11. 12. __ ____ 13. ____ 14. ____ 15. List causes of fetal tachyardia. 16. List causes of fetal bradycardia. 17. What kinds of drugs may decrease variability?_______________________ 18. Identify what constitutes a reassuring fetal heart rate(FHR) patterns? a. b. c. d. 9 Normal Fetal Heart Rate Tachycardia Bradycardia Moderate tachycardia Mild Bradycardia Marked Tachycardia Moderate bradycardia Reflects balance between sympathetic and parasympathetic effect on fetal heart rate FHR changes in association with uterine contractions Caused by fetal head compression Marked Bradycardia Caused by umbilical cord compression Caused by uteroplacental insufficiency Transient increases in FHR a. b. c. d. e. f. g. h. i. j. k. l. m. n. Periodic changes < 100 BPM 110-160 BPM Late Deceleration > 160 for >10 min. Acceleration 100-109 BPM 160-179 BPM Early Deceleration > 180 BPM < 110 for > 10 min. Variability Variable Decels < 70 BPM 19. Identify what constitutes nonreassuring FHR patterns? a. b. c. d. e. Additional Assessment Techniques 20. How is fetal scalp stimulation used to to re-establish fetal well-being? 21. What is the significance of drawing a umblical cord pH? 22. How does the Base Deficit(BD) reflect either metabolic or respiratory acidosis? BD and Base Excess(BE) is derived based on the pH, pCO2, H2CO3, and reflects how much base was “used up” during labor. 10 Cord Blood Gasses Normal Umbilical Artery levels pH 7.20 pCO2 < 60 pO2 > 20 BE < -10 or BD < 10 Severity of pH mild = 7.1 - 7.2 mod = 7.0 - 7.1 severe= < 7.0 usually indicates severe neurological damage Respiratory Acidemia--usually caused by a build-up of CO2 and not severe pH < 7.2 pCO2 > 60 pO2 variable BE < -10 Metabolic Acidemia-- usually caused by hypoxemia and more severe pH < 7.2 pCO2 <60 pO2 <20 BE < -10 Mixed Respiratory and Metabolic Acidemia pH < 7.2 pCO2 > 60 pO2 < 20 BE worse Cord blood gasses are good to have in cases of low Apgar Scores or non-reassuring baselines. 11