Complicated Pregnancy & High-Risk Antepartum; Ch 19-21

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20 Terms

1
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What is the simple high-risk pregancy framework?

  • Recognize cues: Vital signs, symptoms, bleeding/fluid loss, labs, fetal status

  • Name the threat: Perfusion, oxygenation, infection, hemorrhage, seizure, preterm birth

  • Stabilize first: Maternal ABCs, urgent medications, IV access, monitoring, escalation

  • Plan forward: Fetal surveillance, delivery timing, teaching, resources, follow-up


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What are the spectrum of hypertensive disorders ?

  • Chronic hypertension: Present before pregnancy, before 20 weeks, or known preexisting hypertension.

  • Gestational hypertension: New BP ≥140/90 after 20 weeks without proteinuria or other preeclampsia features.

  • Preeclampsia: New hypertension after 20 weeks with proteinuria and/or evidence of maternal organ dysfunction.

  • Preeclampsia with severe features: Severe-range BP and/or significant neurologic, hepatic, renal, hematologic, or pulmonary findings.

  • Eclampsia: New-onset seizure in a patient with preeclampsia when another cause is not more likely.

  • Severe hypertension: systolic ≥160 and/or diastolic ≥110 mm Hg → urgent confirmation and treatment per protocol.


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What is the pathophysiology of preeclampsia: connect pathophysiology to the symptoms?

  • The placenta initiates a systemic maternal endothelial disorder.

  • There is abnormalities in the vasculator when it originally develops thus leading to endothelial function

  • Abnormal placentation: Impaired trophoblastic remodeling → reduced uteroplacental perfusion.→ Endothelial dysfunction: Inflammatory and vascular signaling affects vessels throughout the body.→ Vasoconstriction + leak: Higher vascular resistance + capillary leak → edema and reduced effective perfusion. →Organ / placental injury: Brain, liver, kidney, lungs, platelets, uteroplacental; circulation can be affected.

  • Clinical translation: headache/visual change = brain • RUQ/epigastric pain = liver • oliguria = kidney • dyspnea = pulmonary edema • abnormal fetal growth/tracing = placental disease


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What are the severe features of preeclampsia that indicate organ injury?

  • BP: Persistent severe-range BP ≥160 systolic or ≥110 diastolic

  • Brain: Severe persistent headache or visual symptoms

  • Liver: Severe RUQ/epigastric pain or abnormal liver function

  • Kidney: Worsening renal function / reduced urine output

  • Lungs: Pulmonary edema or new respiratory compromise

  • Blood: Thrombocytopenia / HELLP pattern

  • Nursing habit: symptoms + BP + labs + fetal status are interpreted together—not one cue at a time.


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What should nurses do to assess and care for severe preeclampsia?

  • Immediate assessment

    • Repeat/confirm severe BP appropriately

    • Focused neuro + respiratory assessment

    • Pain, bleeding, edema, reflexes, urine output

    • Continuous fetal assessment when appropriate

  • Prepare + intervene

    • Notify/activate severe-hypertension pathway

    • IV access; CBC/platelets, creatinine, liver tests, urine studies as ordered

    • Give urgent antihypertensive medication per protocol

    • Begin magnesium sulfate when indicated

      • smooth muscle relaxant → to prevent seizure → too much check for resp. distress

  • Anticipate

    • Seizure precautions and quiet environment

    • Strict I&O / fluid awareness

    • Corticosteroids if preterm birth is anticipated and appropriate

    • Possible delivery if maternal or fetal condition worsens

  • Do not delay escalation while waiting for every laboratory result if the patient has severe symptoms or severe-range BP.

  • Persistant low fetal hr indicates poor perfusion


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Magnesium sulfate: Purpose, monitoring, toxicity

  • Why we give it

    • Seizure prophylaxis in severe preeclampsia → Prevent seizure & stop contractions (tocolytic)

    • Treatment/prevention of recurrent eclamptic seizures

    • Also used in selected early preterm birth situations for fetal neuroprotection

    • It is NOT the primary medication for lowering severe blood pressure.

      • Would given antihypertensive to lower bp like labetalol is commonly given in preeclampsia

  • What to monitor

    • Respiratory rate and effort

    • Deep tendon reflexes

    • Level of consciousness

    • Urine output / renal function

    • Maternal vital signs + fetal status

    • Infusion rate and concurrent medications

    • Can be fall risk b/c relaxing muscle

  • Toxicity cues

    • Depressed or absent reflexes

    • Respiratory depression

    • Progressive weakness / decreased LOC

    • Low urine output can increase risk of accumulation

    • Stop infusion / escalate per protocol

    • Calcium gluconate is the antidote.

  • Two medications may be needed: magnesium prevents seizures; antihypertensives treat severe blood pressure.


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Pregestantional diabetes v. Gestational diabetes

  • The nursing priorities overlap, but timing of hyperglycemia changes fetal risk.

  • Pregestational diabetes

    • Type 1 or type 2 diabetes exists before pregnancy.

    • Early-pregnancy glycemic control matters because organ

    • development is occurring.

    • Pregnancy changes insulin needs and can worsen vascular/renal disease.

    • Requires close maternal and fetal surveillance throughout pregnancy.

  • Gestational diabetes

    • Hyperglycemia first recognized during pregnancy in a patient without known preexisting diabetes.

    • Pregnancy hormones increase insulin resistance.

    • For most patients not diagnosed earlier, screening occurs at 24–28 weeks.

    • Nutrition, activity, glucose monitoring, and medications as needed reduce risk.

  • Key distinction: congenital anomaly risk is linked mainly to significant hyperglycemia during early organogenesis in pregestational diabetes.


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How does maternal glucose control affect the fettus and what are the concerns?

  • Maternal hyperglycemia

    • Glucose crosses the placenta.

  • Fetal hyperglycemia

    • Fetal pancreas increases insulin production.

  • Fetal hyperinsulinemia

    • Promotes excess growth and changes neonatal transition.

  • Maternal concerns

    • Preeclampsia / hypertension

    • Polyhydramnios

    • Operative birth / birth trauma risk

    • Future type 2 diabetes after GDM

  • Fetal concerns

    • Large-for-gestational-age growth

    • Shoulder dystocia risk

    • Stillbirth risk rises with poor control

    • Pregestational DM: congenital anomalies with poor early control

  • Newborn concerns

    • Hypoglycemia after cord is cut

    • Respiratory transition concerns

    • Jaundice / polycythemia may occur

    • Feeding + glucose monitoring are priorities


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How is gestational diabetes managed?

  • The nurse translates glucose data into practical daily behaviors and escalation.

  • Monitor

    • Self-monitor blood glucose as prescribed

    • Bring logs / device data to visits

    • Look for patterns, not one isolated value

  • Eat + move

    • Individualized meal pattern

    • Regular meals/snacks as directed

    • Safe activity when not contraindicated

  • Medication

    • Medication when lifestylemeasures do not meet targets

    • Insulin is commonly used during pregnancy

    • Teach injection and hypoglycemia safety

  • Follow through

    • Growth / fetal surveillance based on treatment and control

    • Birth planning individualized

    • Postpartum glucose testing + long-term prevention

    • Teaching goal: make the plan doable in the patient’s real life—work, food access, culture, cost, family support, and health literacy all matter.


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How does pregestational diabeties change in pregnancy?

  • More surveillance is needed because diabetes affects multiple maternal systems.

  • Before / early pregnancy

    • Optimize glucose control when possible

    • Review medications and comorbidities

    • Assess renal, retinal, cardiovascular, thyroid status as appropriate

  • Across pregnancy

    • Insulin needs may shift by trimester

    • Watch closely for hypoglycemia and hyperglycemia

    • Monitor BP, fetal growth, and fetal well-being

  • Birth + postpartum

    • Coordinate intrapartum glucose management

    • Insulin needs typically fall sharply after

    • placental delivery

    • Support breastfeeding and long-term diabetes care

  • Nursing risk check: vomiting + diabetes in pregnancy can become dangerous quickly—assess hydration, glucose, ketones, and signs of DKA per protocol.


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Third Trimester bleeding: Placenta previa v abruption?

  • Pain pattern helps—but maternal and fetal status always come first.

  • Placenta previa- Typical pattern

    • Placenta lies low and may partially or completely cover the cervix.

    • Bleeding is classically painless and may be bright red.

    • Ultrasound establishes placental location.

    • Persistent previa can require cesarean birth.

  • Placenta abruption- Typical pattern

    • Placenta separates from the uterine wall before birth.

    • Bleeding often occurs with abdominal/back pain, tenderness, or frequent contractions.

    • Blood may be visible OR concealed.

    • Maternal hemorrhage, fetal hypoxia, and coagulopathy can develop rapidly.

  • Never let “amount of visible blood” be the only severity measure—abruption can bleed behind the placenta

  • ‘Placenta accreta: placenta grows too deeply into the uterine wall and fails to detach normally after childbirth


<ul><li><p>Pain pattern helps—but maternal and fetal status always come first.</p></li><li><p>Placenta previa- Typical pattern</p><ul><li><p>Placenta lies low and may partially or completely cover the cervix.</p></li><li><p>Bleeding is classically painless and may be bright red.</p></li><li><p>Ultrasound establishes placental location.</p></li><li><p>Persistent previa can require cesarean birth.</p></li></ul></li><li><p>Placenta abruption- Typical pattern</p><ul><li><p>Placenta separates from the uterine wall before birth.</p></li><li><p>Bleeding often occurs with abdominal/back pain, tenderness, or frequent contractions.</p></li><li><p>Blood may be visible OR concealed.</p></li><li><p>Maternal hemorrhage, fetal hypoxia, and coagulopathy can develop rapidly.</p></li></ul></li><li><p>Never let “amount of visible blood” be the only severity measure—abruption can bleed behind the placenta</p></li><li><p>‘Placenta accreta: placenta grows too deeply into the uterine wall and fails to detach normally after childbirth</p></li></ul><p></p>
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How is placenta previa treated to protect against provoking hemorrhage?

  • Diagnosis and severity guide observation versus delivery planning.

  • Assess

    • Maternal VS and symptoms

    • Amount/color of bleeding

    • Fetal heart rate and activity

    • Contractions / uterine activity

    • Hemodynamic signs may precede dramatic visible loss

  • Prepare

    • IV access if significant bleeding

    • CBC, type & screen / crossmatch as ordered

    • `Ultrasound to define placental location

    • Avoid unnecessary cervical manipulation

    • Prepare blood / OR resources if unstable

  • Teach / anticipate

    • Report any recurrent bleeding promptly

    • Activity recommendations are individualized

    • Delivery plan depends on placental location and bleeding

    • Persistent placenta covering the cervix → cesarean delivery

  • If placenta previa is suspected in a bleeding patient, clarify placental location before a routine digital cervical examination.


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How is placenta abruption treated (nursing priorties)?

  • Recognize cues

    • Sudden abdominal or back pain

    • Uterine tenderness / rigidity

    • Frequent contractions

    • Vaginal bleeding may be present or absent

  • Assess severity

    • Maternal tachycardia/hypotension

    • Increasing pain or shock signs

    • Nonreassuring fetal status

    • Falling fibrinogen / coagulopathy may emerge

  • Nursing priorities

    • Rapid maternal and fetal assessment

    • IV access, labs, type/crossmatch, and hemorrhage readiness

    • Continuous fetal monitoring when viable

    • Oxygen/supportive measures as clinically indicated

    • Escalate rapidly; anticipate urgent birth if maternal or fetal status is unstable

    • Prepare for DIC / massive transfusion pathways in severe cases


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Define PROM, PPROM, & preterm labor

  • PROM

    • Rupture of membranes before labor begins.

    • At term, the major concern is timing of labor and infection risk as the interval lengthens.

    • Term PROM is ≥37 weeks.

  • PPROM

    • Preterm prelabor rupture of membranes: membranes rupture before labor AND before 37 weeks.

    • Major concerns: infection, cord complications, fetal compromise, and preterm birth.

  • Preterm labor

    • Regular uterine contractions with cervical change before 37 weeks.

    • Membranes may be intact or ruptured.

    • Management depends on gestational age, maternal/fetal status, and contraindications to prolonging pregnancy.

  • Question to ask first: “Did the membranes rupture? Is labor present? How many weeks?”


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How is suspected rupture of membranes assesed without increasing risk?

  • Confirm the story, maternal status, and fetal response.

  • History

    • Time of gush or ongoing trickle

    • Color / odor / amount

    • Contractions, bleeding, pain

    • Fetal movement

    • Recent intercourse / exam / trauma

    • Gestational age + GBS status if known

  • Assessment

    • Maternal temperature and vital signs

    • Fetal heart rate

    • Uterine activity / tenderness

    • Sterile speculum evaluation as ordered

    • Tests for amniotic fluid per facility protocol

    • Minimize digital cervical exams when PPROM is possible

  • Escalate for

    • Fever / uterine tenderness

    • Fetal tachycardia or nonreassuring status

    • Heavy bleeding / concern for abruption

    • Cord prolapse or abnormal presentation

    • Active labor

    • Maternal instability


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How is prematurity risk with PPROM infection risk managed?

  • The goal is not “keep pregnant at all costs.”

  • Maternal + fetal surveillance

    • Temperature, symptoms, uterine tenderness

    • FHR and fetal movement

    • Contractions / bleeding

    • Labs only when clinically useful

  • Prepare the fetus

    • Antenatal corticosteroids when preterm birth risk and gestational age meet criteria

    • Magnesium sulfate for fetal neuroprotection in selected early preterm birth risk

  • Prevent / treat infection

    • GBS testing and intrapartum prophylaxis as indicated

    • Latency antibiotics are used in appropriate expectant PPROM management

    • Suspected intraamniotic infection changes the plan

  • Know when expectant management stops

    • Maternal infection

    • Significant hemorrhage / abruption

    • Nonreassuring fetal status

    • Active labor or other obstetric indication for delivery

  • Management is gestational-age and condition dependent—students should know the purpose of each intervention, not memorize one universal timeline.


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What are some medications used in pregnancy for different goals?

  • Fetal Preperation: Betamethasone / corticosteroids

    • Goal: accelerate fetal lung and organ maturation when preterm birth is anticipated within an appropriate window.

  • Two Purposes: Magnesium sulfate

    • Goal A: prevent/treat eclamptic seizures in severe hypertensive disease.

    • Goal B: fetal neuroprotection before selected early preterm births.

  • Buy Time: Tocolytic therapy- stop or slow down contractions to delay preterm labor

    • Goal: short-term delay of preterm birth in selected patients so other treatments/transfer can occur.

    • Not appropriate when delaying birth is unsafe.

  • Clinical judgment question: “Is prolonging this pregnancy safer than delivery right now?”


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Rh incompatibility Patho

  • The goal is prevention of maternal sensitization.

  • Rh-negative patient; No anti-D antibodies initially. → Exposure to Rh-positive RBCs; Fetomaternal blood mixing can occur with birth, bleeding, trauma, or procedures. → Maternal anti-D antibodies; Without prophylaxis, immune sensitization can occur. → Future fetal RBC injury; Maternal antibodies cross the placenta and can cause fetal/newborn hemolytic disease.

  • Rho(D) immune globulin supplies passive anti-D and prevents sensitization. It does not remove antibodies once the patient is already sensitized.


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What should nurses consider with Rho(D) immune globulin?

  • Ask: could fetal Rh-positive blood have entered maternal circulation?

  • Routine prevention

    • Unsensitized Rh-negative patient

    • Antepartum prophylaxis around the usual third-trimester timing

    • After birth if the newborn is Rh-positive, with the recommended window

    • Confirm antibody-screen and newborn testing results

  • Potential sensitizing events

    • Pregnancy bleeding

    • Abdominal trauma

    • Amniocentesis / CVS

    • External cephalic version

    • Pregnancy loss / termination depending

    • gestational age and current guidance

    • Other fetomaternal hemorrhage risk

  • Nursing checks

    • Correct patient + Rh status

    • Verify patient is not already sensitized

    • Dose may depend on gestation / volume of fetomaternal hemorrhage

    • Document indication and administration

    • Teach: this is prevention for current/future pregnancies

  • Important nuance: recommendations for RhIG in pregnancy loss before 12 weeks have changed—follow current institutional and obstetric guidance.


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What are some risks that can come from physiology, medications, mental health, substance use, or structural barriers in pregnancy?

  • Medical complexity

    • Cardiac, renal, autoimmune, endocrine, infectious, neurologic or other chronic conditions may destabilize during pregnancy.

  • Age / body / obstetric factors

    • Advanced maternal age, obesity, multifetal pregnancy, prior complications, or assisted reproduction may increase surveillance needs.

  • Mental health + substance use

    • Screen routinely and nonjudgmentally; untreated illness and abrupt medication changes can both carry risk.

  • Social / structural risk

    • Housing, transportation, food access, intimate partner violence, insurance, work leave, language and health literacy can shape outcomes.

  • Nursing stance: screen → ask what matters → reduce stigma → coordinate care → make the plan realistic and safe.