Outpatient Antenatal Testing FLAME LECTURE: 54 STELLER 8.25.14 Learning Objectives Understand the rationale for prenatal outpatient fetal assessment Describe approaches for assessment of fetal well being Prerequisites: FLAME LECTURE 53: Overview of Interpreting Fetal Heart Rate Tracings See also – for closely related topics FLAME LECTURE 54B: The Nonstress Test (NST) and Contraction Stress Test (CST) FLAME LECTURE 56: The Biophysical profile FLAME LECTURE 57: Assessment of fetal movement FLAME LECTURE 59: Assessment of amniotic fluid volume Rationale of Prenatal Outpatient Fetal Assessment Goals Detect uteroplacental insufficiency Prevent stillbirth Avoid unnecessary iatrogenic preterm delivery Physiologic basis: The fetal brain is incredibly sensitive to changes in O2 and pH, and under stress: Chemoreceptor response to acidemia [ vagally-mediated deceleration of the fetal heart rate Fetal movements decrease as the fetus attempts to conserve energy1-2 Blood flow is directed to the brain, heart and adrenals and away from the kidneys [ a decrease in renal perfusion [ a decrease in fetal urine production [ oligohydramnios 1. Olesen AG. Acta Obstet Gynecol Scand. 2004. 2. Manning FA. AJOG 1993 Antepartum Fetal Distress Cascade H Y P O X I A LATE DECELERATIONS APPEAR (CST) ACCELERATIONS DISAPPEAR (NST) BREATHING STOPS (BPP) MOVEMENT CEASES (BPP, FMC) FETAL TONE ABSENT (BPP) Porto, Clin Ob Gyn, 1987 A C I D O S I S Antenatal Assessment Modalities Fetal movement (kick) counting Nonstress test Contraction stress test Biophysical profile (BPP) parameters: fetal breathing, fetal body movements, fetal tone, amniotic fluid volume Modified BPP (mBPP) = NST + AFI Umbilical Artery Doppler velocimetry (for IUGR fetuses only) Indications for Antenatal Testing = Risk factors for uteroplacental insufficiency Pregnancy Maternal APL syndrome, SLE Grave’s disease Asthma, poorly controlled Hemoglobinopathies Cyanotic Chronic Type heart disease renal disease I DM, Type II DM Hypertensive AMA disorders (usually > 38 y.o.) Fetal movement gHTN, Pre-eclampsia A2 GDM Oligohydramnios/ Poly IUGR Late-term/Post-term Isoimmunization Previous unexplained fetal demise Monochorionic or discordant twins Third trimester vaginal bleeding Timing of antepartum surveillance WHEN TO START? WHY TO START? HOW OFTEN TO PERFORM? No large clinical trials to guide recommendations of initiation and frequency of testing THE UCI APPROACH - Initiation 26 wks 32 - 34 40 41 @ Dx Individualize DM: DFR Htn IUGR Diabetes: Class BC Gestation Diabetes Post Dates PIH Decrease FM cHTN, SLE Immune disorders IUGR Rh Isoimmun Antiphospholipid antibody syndrome Cardiac, pulmonary or renal disease Discord. Twins Mono-mono twins Mono-di twins Third trimester bleeding Hematol. disease THE UCI APPROACH – Frequency Twice AFI CST weekly NST with weekly AFI twice weekly in postdates or AFI < 8.0 alternating w/ NST q3-4 days in DM AFI is not as useful in DM, increased AFI Twins NST with IUGR/discordance: twice weekly, UAD + DVP weekly Testing NST < 28 weeks: BPP primarily is often not reassuring or equivocal due to neurologic immaturity REASSURANCE? Incidence of stillbirth within 1 week after a normal fetal assessment modality3-5 1.9/1000 NSTs - NPR of 99.8% 0.3/1000 CSTs – NPR of 99.9% 0.8/1000 BPPs – NPR of 99.9% 0.8/1000 mBPPs – NPR of 99.9% 0/214 Dopplers in IUGR fetuses – NPR of 100%6 They do not predict stillbirths related to acute changes in maternal-fetal status Abruptio placentae Umbilical cord accident Achilles heel is high false positive rate (approx 35% CST, 55% NST) Abnormal testing… now what? Fix the offending disease process if possible i.e DKA, PNA Perform a ‘back-up’ test (CST, BPP or prolonged monitoring), or repeat testing in short intervals7 Ex. Decreased fetal movement + nonreactive NST Term: CST [ deliver if positive or equivocal Significantly preterm: BPP [ deliver, continuously monitor or retest in 24 hours, depending on results If not reassured, hospitalize and weigh the risks and benefits of expediting delivery following consideration of gestational age and the disease state THE UCI APPROACH: In general NST + AFI Both Normal Nonreactive / AFI < 5 CST Or BPP 8 Negative Retest 3-4 days Consider delivery Positive <6 CFM vs. daily NST IMPORTANT LINKS PRACTICE BULLETIN 145 - Antepartum Fetal Surveillance OTHER REFERENCES 1. Olesen AG. Acta Obstet Gynecol Scand. 2004. 2. Manning FA. AJOG 1993 3. Freeman RK. AJOG 1982 4. Miller DA. AJOG 1996. 5. Manning FA. AJOG. 1987. 6. Almstrom H. Lancet. 1992 7. Manning FA. AJOG. 1990.