Obstetric Complications Flashcards

1
Q

Preterm birth is defined as a birth that occurs after 20 weeks but before 37 completed weeks of gestation. How is preterm labor (PTL) diagnosed?

A

Uterine contractions accompanied with cervical change or cervical dilation of 2 cm and/or 80% effaced

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2
Q

Etiologies of preterm labor

A
Spontaneous
Multiple gestations
Preterm premature rupture of membranes
Pregnancy-associated HTN
Cervical incompetence or uterine anomalies
Antepartum hemorrhage
Intrauterine growth restriction (IUGR)
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3
Q

Risk factors for PTL

A

SES factors: African American 2x more likely than Caucasian; Decreased access to prenatal care; High stress levels, poor nutrition

Medical/obstetric factors: previous hx of PTL, hx of 2nd trimester abortion, repeated 1st trimester abortions, bleeding in first trimester, UTI/genital tract infection, multiple gestation, uterine anomalies, polyhydramnios, incompetent cervix

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4
Q

4 main pathways addressed in prevention of PTL

A

Infection (cervical)
Placental-vascular
Psychosocial stress/work strain
Uterine stretch

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5
Q

How is PTL prevented via infection-cervical pathway?

A

Treat bacterial infections associated with preterm labor: Bacterial vaginosis, Group B strep, Gonorrhea, Chlamydia

[there is a link between infection and progressive changes in cervical length, and cervical length is a predictor for preterm birth risk]

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6
Q

The relative risk of PTL increases as cervical length decreases. What are screening methods to determine cervical length?

A

Routine screening with US

Fetal fibronectin (FFN) — released in response to disruption of membranes as with uterine activity, cervical shortening, or infection [negative predictive value is good, positive predictive value is low]

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7
Q

How is the placental vascular pathway involved in risk for PTL?

A

Alteration of placental vasculature at the level of placental-decidual-myometrial interface may result in poor fetal growth, which is a risk factor for PTL as well as growth restriction and preeclampsia

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8
Q

How is the stress-strain pathway involved in risk for PTL?

A

Mental and physical stress induce release of cortisol and catecholamines, which are associated with uterine contractions

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9
Q

Symptoms of preterm labor

A

Menstrual like cramping, low/dull backache, pelvic pressure, increase in discharge/bloody discharge, and uterine contractions

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10
Q

Management of PTL

A

Initial assessment with cervical exam to assess dilation, effacement, and fetal presenting part

Evaluate for underlying correctable problems such as infection (culture for group B strep)

External monitoring for uterine activity and fetal HR

Reevaluate cervix hourly and administer oral or IV hydration

CBC, urinalysis, and urine culture

Obtain US (fetal presentation, growth, amniotic fluid volume, r/o congenital anomalies)

Consider tocolytics

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11
Q

Indications/criteria to begin tocolytics in PTL

A

2 cm dilation and/or 80% effaced, or made cervical change; and gestational age <34 weeks and no contraindications

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12
Q

3 tocolytics used in PTL

A

Magnesium sulfate

Nifedipine

Prostaglandin Synthetase Inhibitors (Indomethacin)

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13
Q

In the US, the tocolytic agent of choice in PTL is magnesium sulfate. Therapeutic serum levels range from 5.5 to 7.0 mg/dL. Typically a 6g loading dose is given IV, then 3g/hr for continuous maintenance. Therapy is continued until both doses of _____ are administered, and may be titrated down if uterine activity stops. Some studies have shown magnesium sulfate may play a role in _______ and possibly protects against cerebral palsy. It is currently indicated for use in less than 32 weeks gestation PTL.

A

Steroids

Neuroprotection

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14
Q

Side effects of magnesium sulfate

A

Maternal: feeling of warmth and flushing, N/V, respiratory depression (with high serum levels), cardiac conduction defects and arrest (high serum levels)

Neonate: loss of muscle tone, drowsiness, lower apgar scores

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15
Q

Oral agent effective in suppressing PTL with minimal maternal and fetal side effects including HA, cutaneous flushing, hypotension, and tachycardia

A

Nifedipine

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16
Q

Tocolytic used on short term basis, mostly for extreme prematurity

A

Prostaglanin synthetase inhibitors

17
Q

Complications of prostaglandin synthetase inhibitor (indomethacin) when used as PTL tocolytic

A

Oligohydramnios

Premature closure of fetal ductus arteriosus —> pulmonary HTN and heart failure

Increased risk of necrotizing enterocolitis and intracranial hemorrhage

18
Q

When is ibuprofen indicated for tocolysis?

A

Not used for primary tx of preterm labor, but used to decrease uterine activity not associated with labor — to the point that hyperactive contractions are interfering with pt’s life

19
Q

Drug given to accelerate premature fetal lung maturation

A

Glucocorticoids (betamethasone, dexamethasone)

Given between 22-34 weeks gestation

Effects last 7 days

20
Q

A single course of ______ is recommended for pregnant women between 34-36 weeks of gestation at risk of preterm birth w/i 7 days, and who have not received a previous course of antenatal corticosteroids

A

Betamethasone

21
Q

Lower limit of preterm viability in weeks and grams

A

23-24 weeks or 500 grams

22
Q

PTL intervention used in women with previous hx of spontaneous PTL/PPROM, given weekly from 16-36 wks

A

IM progesterone (Makena)

23
Q

PTL intervention used in women with a shortened cervix (<2.5cm)

A

Vaginal progesterone (prometrium or crinone)

Pessary (arabin pessary)

24
Q

The etiology of PROM is unknown. What are some risk factors?

A

Vaginal/cervical infections
Abnormal membranes
Incompetent cervix
Nutritional deficiencies

25
Q

Why shouldn’t you check the cervix of a presumed ruptured preterm patient?

A

Increases the risk of infection, especially with prolonged latency before delivery

26
Q

3 tests used for confirmation of PROM

A

Pooling
Nitrazine paper
Ferning

[may also use US to evaluate amniotic fluid volume]

Note: false positives on nitrazine may be caused by urine, semen, cervical mucous, blood, or vaginitis; false negatives may occur with remote PROM with no remaining fluid or with minimal leakage

27
Q

In the management of preterm premature rupture of membranes (PPROM), the risk of preterm delivery must be balanced with the risk of infection, as an intact amnionic sac provides a barrier to ________, an infection of the membranes and fetal infection associated with about 30% of preterm deliveries

A

Chorioamnionitis

28
Q

Management of PPROM depends on gestational age at time of rupture, amniotic fluid index, fetal status, and maternal status. The goal is to continue the pregnancy until lung profile is mature. Most will deliver at ____ weeks regardless of fetal lung maturity (earlier with dx of chorioamnionitis)

A

34

29
Q

Signs/symptoms of chorioamnionitis

A

Maternal temp >100.4
Fetal or maternal tachycardia
Tender uterus
Foul smelling amniotic fluid/purulent discharge

30
Q

ACOG recommendations for abx and tocolytic usage in PPROM

A

For abx, ACOG recommends 48 hr course of ampicillin and erythromycin/azithromycin followed by 5 days of amoxil and erythromycin

For tocolytics, ACOG does not recommend for or against, they may be used if there is no evidence for chorioamnionitis and primary purpose is to have time to get steroid tx to baby

31
Q

Define intrauterine growth restriction (IUGR) vs. small for gestational age (SGA)

A

IUGR: birth weight of newborn is below 10% for given gestational age

SGA: birth weight at lower extreme of normal birth weight distribution

32
Q

Growth restricted fetuses are at risk for what complications?

A
Meconium aspiration
Asphyxia
Polycythemia
Hypoglycemia
Mental retardation
Adult onset of conditions such as HTN, diabetes, and atherosclerosis
33
Q

Maternal causes of IUGR

A

Poor nutritional intake/maternal low body weight

Cigarette smoking, drug abuse, alcoholism

Cyanotic heart disease

Pulmonary insufficiency (i.e., poorly controlled asthma)

Antiphospholipid syndrome

Hereditary thrombophilias

Collagen vascular dz

34
Q

Placental causes of IUGR involve insufficient substrate transfer through placenta as well as defective trophoblastic invasion. What conditions may result in placental insufficiency?

A

HTN (preexisting or gestational)

Renal disease

Placental or cord abnormalities such as velamentous cord insertion

Diabetes

35
Q

Fetal causes of IUGR

A

Intrauterine infections — listeriosis, TORCH

Congenital anomalies/genetic disorders

Multiple gestations

Chromosomal abnormalities

36
Q

How is IUGR diagnosed?

A

Primary screening test is PE of fundal height. If fundal height lags more than 3 cm behind the gestational age, then order an ultrasound

US is used routinely for high risk conditions that predispose to IUGR such as HTN, renal dz, diabetes, drug abuse, antiphospholipid syndrome, lupus

37
Q

Pre-pregnancy management of IUGR involves optimization of disease processes (i.e., blood sugar control, HTN control)

Antepartum management of IUGR involves decreasing any modifiable risk factors (improve nutrition, stop smoking, etc.) with the goal of delivering before fetal compromise but after fetal lung maturity. What tests are monitored in antepartum period?

A

Non-stress test 2x/week

Biophysical profile

Doppler studies of umbilical a. (Umbilical flow velocity waveform of normally growing fetuses is characterized by high-velocity diastolic flow, whereas with intrauterine growth restriction there is diminution of umbilical a. diastolic flow)

38
Q

T/F: Babies with IUGR require C-section delivery

A

False — IUGR is not an indication for C-section, but fetuses have less reserve and may have intolerance of labor

Require continuous fetal monitoring and other factors may necessitate C-section

39
Q

What tests should be monitored after birth of baby with IUGR?

A

Monitor neonatal blood glucose, as these babies have less hepatic glycogen stores

Monitor respiratory status as RDS is more common