UNIT 2 HIGH RISK PREGNANCY CHAPTER 10,11,12 Flashcards

1
Q

What are some risk factors of HIGH Risk Pregnancy

A

Biophysical
Psychosocial
Demographic
Environmental

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2
Q

What would indicate the pregnant mother is at high risk Biohysically?

A

Biophysical risks include factors that originate within the mother or fetus and affect the development or functioning of either one or both. Examples include genetic disorders, nutritional and general health status, and medical or obstetric-related illnesses. Box 10.2 lists common risk factors for several pregnancy-related problems.
EXAMPLES
Poorly controlled diabetes mellitus
Fetomaternal hemorrhage
Fetal congenital anomalies (e.g., gastrointestinal obstruction, central nervous
system abnormalities)
Genetic disorders
Twin-to-twin transfusion syndrome

Genetic considerations: Genetic factors may interfere with normal fetal or neonatal development, result in congenital anomalies, or create difficulties for the mother. These factors include defective genes, transmissible inherited disorders and chromosomal anomalies, multiple gestation, large fetal size, and ABO incompatibility.

  • Nutritional status: Adequate nutrition, without which fetal growth and devel- opment cannot proceed normally, is one of the most important determinants of pregnancy outcome. Conditions that influence nutritional status include the following: adolescent pregnancy; three pregnancies in the previous 2 years; tobacco, alcohol, or drug use; inadequate dietary intake because of chronic illness or food fads; history of bariatric surgery; inadequate or excessive weight gain; and hematocrit value less than 33%.
  • Medical and obstetric disorders: Complications of current and past pregnancies, obstetric-related illnesses, and pregnancy losses put the woman at risk
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3
Q

What would indicate the pregnant mother is at high risk Psychosocially?

A

Psychosocial risks consist of maternal behaviors and adverse life events that have a negative effect on the health of the mother or fetus. These risks may include emotional distress, history of depression or other mental health problems, disturbed interpersonal relationships such as intimate partner violence, substance use or abuse, inadequate social support, and unsafe cultural practices.

Smoking: Risks include low birth weight infants, higher neonatal mortality rates, increased rates of miscarriage, and increased incidence of prelabor rupture of membranes. These risks are aggravated by low socioeconomic status, poor nutritional status, and concurrent use of alcohol.

  • Caffeine: Birth defects in humans have not been related to caffeine con- sumption. However, pregnant women who consume more than 200 mg of caffeine daily (equivalent to about 12 ounces of coffee per day) may be at increased risk for giving birth to infants with intrauterine growth restriction (IUGR).
  • Alcohol: Although the exact effects of alcohol in pregnancy have not been quantified and its mode of action is largely unexplained, it exerts adverse effects on the fetus, resulting in fetal alcohol syndrome, fetal alcohol effects, learning disabilities, and hyperactivity.
  • Drugs: The developing fetus may be affected adversely by drugs through several mechanisms. They can be teratogenic, cause metabolic disturbances, produce chemical effects, or cause depression or alteration of central nervous system (CNS) function. This category includes medications prescribed by a health care provider or bought over the counter, and commonly abused drugs such as heroin, cocaine, and marijuana (see Chapter 11 for more information about drug and alcohol abuse).
  • Psychologic status: Childbearing triggers profound and complex physiologic, psychologic, and social changes, with evidence to suggest a relationship be- tween emotional distress and birth complications. This risk factor includes conditions such as specific intrapsychic disturbances and addictive lifestyles; a history of child abuse or intimate partner violence; inadequate support systems; family disruption or dissolution; maternal role changes or conflicts; noncompliance with cultural norms; unsafe cultural, ethnic, or religious prac- tices; and situational crises.
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4
Q

What would indicate the pregnant mother is at high risk Demographically?

A

Sociodemographic risks arise from the context in which the mother and family live. These risks may place the mother and fetus at risk. Examples include lack of prenatal care, low income, single marital status, and living as an ethnic minority within a context of structural racism (see Box 10.1).

Low income: Poverty underlies many other risk factors and leads to inade- quate financial resources for food and prenatal care, poor general health, in- creased risk for medical complications of pregnancy, and greater prevalence of adverse environmental influences.
* Lack of prenatal care: Failure to diagnose and treat complications early is a major risk factor arising from financial barriers or lack of access to care;
* Marital status: The increased mortality and morbidity rates for unmarried women, including an increased risk for preeclampsia, are often related to in- adequate prenatal care and a young childbearing age.
* Parity
The number of previous pregnancies is a risk factor associated with age and includes all first pregnancies, especially a first pregnancy at either end of the childbearing age continuum. The incidence of preeclampsia and dystocia is increased with a first birth.
* Age: Women at both ends of the childbearing age spectrum have an in- creased incidence of poor outcomes; however, age may not be a risk factor in all cases. Physiologic and psychologic risks should be evaluated.
* Adolescents: Possible pregnancy and birth complications include anemia, preeclampsia, prolonged labor, and contracted pelvis and cephalopelvic dis- proportion. Long-term social implications of early motherhood are lower edu- cational attainment, lower income, increased dependence on government support programs, higher divorce rates, and higher parity.
* Mature mothers: The risks to older mothers (over 35 years of age) are not from age alone but from other considerations such as number and spacing of previ- ous pregnancies, genetic disposition of the parents, medical history, lifestyle, nutrition, and prenatal care.
* Ethnicity: Although ethnicity by itself is not a major risk, race is associated with some poor pregnancy outcomes. In the United States, for example, African American women have rates of preterm birth that are almost twice as high as those of other racial and ethnic groups.

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5
Q

What would indicate the pregnant mother is at high risk Environmentally?

A

Various environmental substances can affect fertility and fetal development, the chance of a live birth, and the child’s subsequent mental and physical develop- ment. Environmental influences include infections, radiation, chemicals such as mercury and lead, therapeutic drugs, illicit drugs, industrial pollutants, cigarette smoke, stress, and diet. Paternal exposure to mutagenic agents in the workplace has been associated with an increased risk for miscarriage.

Toxoplasmosis results from infection with a common parasite found in cat feces and contaminated food. It can cause serious complications for pregnant women and people with weakened immune systems.
Symptoms include muscle pain, fever, and headache, all of which can last for weeks.

DO NOT USE OR DO
eating raw food
and handling cat litter

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6
Q

What statement would be considerate of a patients pyschosocial status (pregnant woman)?

A. Is there anything that has been causing stress at home are you using any drugs to cope?
B. Is there any genetic disorders that run in your family that might affect the baby?

A

A. Is there anything that has been causing stress at home are you using any drugs to cope?

Psychosocial risks consist of maternal behaviors and adverse life events that have a negative effect on the health of the mother or fetus. These risks may include emotional distress, history of depression or other mental health problems, disturbed interpersonal relationships such as intimate partner violence, substance use or abuse, inadequate social support, and unsafe cultural practices.

Label of a high-risk pregnancy may
result in:
* Increased sense of vulnerability
* Stress related to diagnoses
* Ambivalence regarding pregnancy
* Inability to accomplish tasks of
parenthood
* Fearful for well-being of mother

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7
Q

What is the function of the Coombs test?

A

Rh incompatibility; detects antibodies for incompatibility to
maternal antigens
* Cell free DNA in maternal blood
* A new screening message for noninvasive prenatal genetic
diagnosis
* Fetal Rh status; Fetal gender
* Paternally transmitted single gene disorders
* Works by amplifying cell free DNA

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8
Q

What does IUGR stand for? What type of pregnant patients?

A

Intrauterine Growth Restriction

A condition in which a baby doesn’t grow to normal weight during pregnancy.

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9
Q

What is Electronic Fetal Monitoring

A
  • Goal
  • to determine if intrauterine
    environment supportive to fetus
  • Non-stress test (fetal activity
    determination) REACTIVE IS GOOD
  • Procedure
  • Interpretation 32 weeks
    gestation before valid
  • Vibroacoustic stimulation
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10
Q

What does Fetal Monitoring Movement consist of ?

A

baby kicks

5 kicks every hour is good

Daily fetal movement count
(DFMC)
* Simple yet valuable method to
evaluate fetal wellbeing
* Several methods can be used
to count
* Once a day for 60 minutes
* 2 to 3 times daily
* 10 movements in 2-hour
period optimal

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11
Q

What is one of the most noninvasive as simplest ways to monitor fetal well being?

A. Daily fetal movement count
B. Non stress test

A

A. Daily fetal movement count

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12
Q

Is it important to eat before Daily fetal movement count?
Yes
No

A

Yes

  • Eat meal or snack before
    counting
  • Limit external stimuli
    to concentrate on kicks
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13
Q

Would you increase external stimuli when starting the daily fetal movement count?

Yes
No

A

No

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14
Q

Indications for use of Ultrasonography?

A

Diagnostic ultrasonography is an important, safe technique in ante- partum fetal surveillance. It is considered by many to be the most valuable diagnostic tool used in obstetrics. It provides critical informa- tion to health care providers regarding fetal activity and gestational age, normal versus abnormal fetal growth curves, fetal and placental anatomy, fetal well-being, and visual assistance that increases the safety of invasive tests that must be performed

*Fetal heart rate activity
* Gestational age
* Fetal growth
* Fetal anatomy
* Fetal genetic disorders
* Placental position &
function
* Adjunct to invasive tests

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15
Q

Magnetic
resonance
imaging (MRI)

A

Magnetic resonance imaging (MRI) is a noninvasive radiologic technique used for obstetric and gynecologic diagnosis. Similar to computed tomography (CT), MRI provides excellent pictures of soft tissue. Unlike CT, ionizing radiation is not used. Therefore, vascular structures within the body can be visualized and evaluated without injecting an iodinated contrast medium, thus eliminating any known biologic risk. Similar to that of sonography, MRI is noninvasive and can provide images in multiple planes, but no interference occurs from skeletal, fatty, or gas-filled structures, and imaging of deep pelvic structures does not require a full bladder.

Fetal structure & growth
* Placenta (position, density, &
presence of gestational
trophoblastic disease)
* Quantity of amniotic fluid
* Maternal structures (uterus,
cervix, adnexa, and pelvis)
* Biochemical status of tissues &
organs
* Soft tissue, metabolic, or
functional anomalies

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16
Q

Which of the following statements indicate the fetus is well?

A.Nonreactive stress Test
B. Reactive stress test

A

B. Reactive stress test

NST results are either reactive (Fig. 10.9) or nonreactive (Fig. 10.10). Box 10.7 lists the criteria for both results. A reactive NST is considered normal, while a nonreactive test requires further evaluation. The test- ing period is often extended, usually for an additional 20 minutes, with the expectation that the fetal sleep state will change and the test will become reactive. During this time, vibroacoustic stimulation (see later discussion) may be used to stimulate fetal activity. If the test does not meet the criteria after 40 minutes, a contraction stress test or BPP should be performed. Once the NST is initiated, it is usually repeated once or twice weekly for the remainder of the pregnancy (G

17
Q

Reactive nonstress test

A

A Reactive Nonstress Test. Accelerations of the fetal heart greater than 15 beats/min and that last longer than 15 seconds can be identified. When the patient appreciates a fetal movement, she presses an event marker on the monitor, which creates arrows on the lower portion of the tracing.

Two accelerations in a 20-min period, each lasting at least 15 s and peaking at least 15 beats/min above the baseline. (Before 32 weeks of gestation, an acceleration is defined as a rise of at least 10 beats/min lasting at least 10 seconds from onset to offset.)

The nonstress test (NST) is the most widely applied technique for antepartum evaluation of the fetus. The basis for the NST is that the normal fetus produces characteristic heart rate patterns in response to fetal movement, uterine contractions, or stimulation

18
Q

Nonreactive stress test

A

Nonreactive test: A test that does not demonstrate at least two qualifying accelerations within a 20-min window (see Fig. 10.10).

19
Q

Contraction stress test

A

The contraction stress test (CST) or oxytocin challenge test (OCT) was the first widely used electronic fetal assessment test.

This test can either be positive or negative,

Positive is BAD
Late decelerations occur with 50% or more of contractions, even if there are fewer than three contractions in 10 min

Negative is GOOD
At least three uterine contractions in a 10-min period, with no late or significant variable decelerations

20
Q

Should the contraction stress test be done for women who are at risk for preterm labor?

A. No
B. Yes

A

A. No

In general, the CST cannot be performed on women who should not give birth vaginally at the time the test is done.

The CST should not be per-formed in patients who are at high risk for preterm labor, including those with pre-term labor rupture of membranes, multiple gestation, and cervical insufficiency. The test should also be avoided in patients with conditions in which uterine contractions could be dangerous, such as placenta previa and previous classical incision for cesarean birth or other uterine surgery

Because of these disadvantages, the CST is generally used as a backup, rather than a primary method of antepartum testing.

21
Q

Chorionic villus sampling (CVS)

A
  • Earlier diagnosis & rapid results
  • Performed @ 10-13 weeks gestation
  • Removal small tissue specimen from
    fetal portion of placenta
  • Chorionic villi originate in zygote
  • Tissue reflects genetic makeup of
    fetus

Earliest test to detect genetic disorders
This test is invasive. mainly done for women who have past medical history of genetic disorders and or advanced age mothers or geriatric mothers

22
Q

What is this protein”alpha-fetoprotein (AFP)” used to indicate?

A

Maternal serum alpha-fetoprotein (AFP) levels are used as a screening tool for NTDs in pregnancy. Through this technique, approximately 85% to 92% of open NTDs and almost all cases of anencephaly can be detected early (Wapner & Dugoff, 2019). Screening is recommended for all pregnant women.

23
Q

Percutaneous umbilical blood sampling (PUBS)

A

Direct access to the fetal circulation during the second and third tri- mesters is possible through percutaneous umbilical blood sampling (PUBS) (also called cordocentesis).

24
Q

When are amniocentesis done during what is the range of gestation?

A

15-26weeks

  • Indication for use
  • Genetic concerns
  • Mother over 35 years
  • Family history chromosomal
    abnormalities
  • Fetal maturity
  • L/S and S/A ratios
  • Fetal hemolytic disease
25
Q

Maternal Complications of Amniocentesis

A
  • Hemorrhage
  • Feto-maternal hemorrhage- mixing of blood with fetal and mom’s blood
  • Infection
  • Labor
  • Abruptio placentae
  • Damage to intestines or
    bladder
  • Amniotic fluid embolism
26
Q

Fetal Complications of Amniocentesis

A
  • Death
  • Hemorrhage
  • Infection (amniotitis)
  • Injury from needle
  • Risks minimized by using
    ultrasound to direct the
    procedure
27
Q

What pain does Ectopic pregnancy experience

A

Most cases of ectopic (tubal) pregnancy are diagnosed before rupture based on the three most classic symptoms: (1) abdominal pain, (2) delayed menses, and (3) abnormal vaginal bleeding (spotting). Ab- dominal pain occurs in almost every case. It usually begins as a dull, lower-quadrant pain on one side. The discomfort can progress from a dull pain to a colicky pain when the tube stretches, to sharp, stabbing pain. It progresses to a diffuse, constant, severe pain that is generalized throughout the lower abdomen.

28
Q

What is the pain experienced during ruptures ectopic pregnancy?

A

If the ectopic pregnancy is not diagnosed until after rupture has oc- curred, referred shoulder pain may be present in addition to generalized, one-sided, or deep lower quadrant acute abdominal pain. Referred shoul- der pain results from diaphragmatic irritation caused by blood in the peritoneal cavity.

29
Q

Risk factors for preterm labor

A
  • History of a previous spontaneous preterm birth between 16 and 36 weeks of gestational
  • History of genital tract colonization, infection, or instrumentation
  • Blackrace
  • Bleeding of uncertain origin in pregnancy
  • Uterine anomaly
  • Use of assisted reproductive technology
  • Multifetal gestation
  • Cigarette smoking, substance abuse
  • Prepregnancy underweight (BMI ,19.6) and prepregnancy obesity (BMI .30)
  • Periodontal disease
  • Limited education and low socioeconomic status
  • Late entry into prenatal care
  • High levels of personal stress in one or more domains of life
30
Q

What does Alpha Feto-Protein detect

A

Can identify genetic disorders and neural tube defects

31
Q

What does Human Chorionic Gonadotropin detect

A

high levels may indicate Trisomy 21 ( Down syndrome)

32
Q

What does Unconjugated Estriol detect

A

Low levels may indicate Trisomy 18 (Edwards Syndrome)

33
Q

What does Inhibit A detect

A

A marker that is more sensitive Down syndrome than other test