Protocols for High-Risk Pregnancies. Группа авторов

Protocols for High-Risk Pregnancies - Группа авторов


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      12 Mari G, Deter RL, Carpenter RL, et al. Collaborative group for doppler assessment of the blood velocity in anemic fetuses. Noninvasive diagnosis by Doppler ultrasonography of fetal anemia due to maternal red‐cell alloimmunization. N Engl J Med 2000; 342:9–14.

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       Michael P. Nageotte1,2

      1 Miller Children’s and Women’s Hospital, Long Beach, CA, USA

      2 Department of Obstetrics and Gynecology, University of California, Irvine, CA, USA

      Antepartum fetal testing is utilized to assess fetal well‐being, especially in the complicated pregnancy. Several tests are utilized including the nonstress test (NST), the biophysical profile (BPP), the modified BPP, and the contraction stress test (CST).

      The NST is currently the most common means of evaluation of fetal oxygenation status during the antepartum period. Less intensive than the CST in many regards, the NST evolved as an excellent means of fetal assessment following observations that the occurrence of two or more accelerations of the fetal heart during a CST most often predicted a negative CST while the absence of these accelerations of baseline fetal heart rate was associated with a positive test and poor perinatal outcome. The basic premise of the NST is that the fetal heart will accelerate its rate with fetal movement if the fetus is not acidotic or depressed neurologically.

      A reactive NST is defined by the presence of two or more accelerations of the fetal heart rate of at least 15 beats per minute lasting for at least 15 seconds within 20 minutes. Other definitions of reactivity have been proposed with a requirement of two or more accelerations in as little as 10 minutes before the test is considered reactive. If such accelerations are not elicited either spontaneously or with repeated vibroacoustic stimulation within 40 minutes of monitoring, the NST is interpreted as nonreactive. Options for further management include admission to hospital for delivery or extended monitoring or, more commonly, some form of backup test (e.g., a CST or BPP) is performed immediately. If the variable decelerations are repetitive or prolonged (lasting greater than one minute), the test is read as equivocal and a back‐up test is indicated at that time.

      The fetal BPP is a frequently utilized method of antepartum fetal surveillance. The BPP score is a composite of four acute or short‐term variables (fetal tone, movement, breathing, and nonstress test) and one chronic or long‐term variable (amniotic fluid index). All four short‐term variables of the BPP are regulated by the fetal central nervous system (CNS). The fetal CNS is highly sensitive to decreases in the level of oxygenation and these biophysical variables are directly influenced by changes in the state of oxygenation of the fetus.

      In the presence of progressive hypoxemia, clinical studies have confirmed that reactivity is the first biophysical variable to disappear. This is followed by the loss of fetal breathing and subsequently the loss of fetal movement. Fetal tone is the last variable to be lost in the presence of ongoing in utero hypoxemia.

      Fetal urine production is the predominant source of amniotic fluid volume and is directly dependent upon renal perfusion. In response to sustained fetal hypoxemia, there is a long‐term adaptive response mediated by chemoreceptors located in the aortic arch and carotid arteries. This results in chemoreceptor‐mediated centralization of fetal blood flow by differential channeling of blood to vital organs in the fetus (brain, heart, adrenals), at the expense of nonessential organs (lung, kidney) by means of peripheral vasoconstriction. In cases of prolonged or repetitive episodes of fetal hypoxemia, there is a persistent decrease in blood flow to the lungs and kidneys resulting in a reduction in the amniotic fluid production leading to oligohydramnios. Amniotic fluid volume, therefore, is a reflection of chronic fetal condition. On average, it takes approximately 13 days for a fetus to progress from a normal to an abnormal amniotic fluid volume.

      Source: Based on Manning et al. (1980). Reproduced with permission of Elsevier.

Biophysical variable Normal (score = 2) Abnormal (score = 0)
Nonstress test Reactive: More than two accelerations of greater than 15 bpm for more than 15 seconds in 20 minutes Nonreactive: Less than two accelerations of greater than 15 bpm for more than 15 seconds in 20 minutes
Fetal breathing movements More than one episode of more than 30 seconds in 30 minutes Absence or less than 30 seconds in 30 minutes
Gross body movements More than three discrete body/limb
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