Pregnancy-Induced Hypertension (PIH): Comprehensive Nursing Notes
Evidence-based nursing knowledge for optimal maternal and fetal outcomes

Table of Contents
Introduction
Pregnancy-induced hypertension (PIH) is a significant obstetrical complication affecting 5-10% of all pregnancies worldwide. It represents a spectrum of hypertensive disorders that occur during pregnancy, typically after 20 weeks gestation. PIH is a leading cause of maternal and perinatal morbidity and mortality globally, making it a critical area of focus for nursing care.
PIH was historically referred to as “toxemia” due to the belief that it was caused by maternal toxins in response to fetal proteins. While no such toxins were ever identified, the term illustrates the systemic nature of the condition. Modern understanding of PIH encompasses several distinct conditions, all characterized by elevated blood pressure during pregnancy, with potentially serious outcomes for both mother and fetus.
As nurses, our role in the management of PIH is multifaceted – from early detection through assessment and monitoring to active intervention and patient education. These comprehensive notes aim to provide nursing students with an evidence-based understanding of pregnancy-induced hypertension, its pathophysiology, classifications, assessment techniques, and appropriate nursing interventions.
Pathophysiology
The exact pathophysiology of pregnancy-induced hypertension remains incompletely understood, but significant advances have been made in understanding the underlying mechanisms. Current research indicates that PIH develops through a complex interplay of factors:
Placental Development Abnormalities
The primary pathological process appears to originate in the placenta:
- Abnormal trophoblastic invasion: During normal pregnancy, trophoblast cells invade the spiral arteries, replacing the muscular and elastic tissues with fibrinoid material. This physiological change creates low-resistance vessels that can accommodate increased blood flow to the placenta.
- Impaired spiral artery remodeling: In PIH, there is inadequate/shallow trophoblastic invasion of the spiral arteries in the myometrium. The arteries remain narrow and retain their muscular walls.
- Reduced placental perfusion: The failure of spiral arteries to dilate appropriately leads to placental hypoperfusion and ischemia.
Endothelial Dysfunction and Systemic Response
Placental ischemia triggers a cascade of events leading to widespread endothelial dysfunction:
- Angiogenic imbalance: The ischemic placenta releases excessive amounts of anti-angiogenic factors such as soluble fms-like tyrosine kinase-1 (sFlt-1) and soluble endoglin (sEng).
- Reduction in pro-angiogenic factors: There are decreased levels of vascular endothelial growth factor (VEGF) and placental growth factor (PlGF).
- Systemic endothelial damage: This angiogenic imbalance induces widespread endothelial cell dysfunction in maternal blood vessels.
Memory Aid: The “Two-Stage Disorder”
Stage 1: “Poor Placentation” (Reduced placental perfusion)
Stage 2: “Problematic Proteins” (Release of anti-angiogenic factors)
Remember: PIH = Poor Placentation → Problematic Proteins → Pressure Increase in Hypertension
Systemic Effects
The endothelial dysfunction leads to multiple systemic effects:
- Increased vascular sensitivity to vasopressors like angiotensin II
- Vasoconstriction leading to hypertension
- Increased capillary permeability causing edema
- Activation of coagulation cascade resulting in microthrombi
- End-organ damage affecting kidneys, liver, brain, and other vital organs
Cardiovascular Changes
Normal pregnancy involves:
- Increased cardiac output
- Decreased systemic vascular resistance
- Decreased sensitivity to vasopressors
In PIH, these adaptations are altered:
- Increased systemic vascular resistance
- Increased sensitivity to vasopressors
- Reduced plasma volume (hemoconcentration)
Classification of Hypertensive Disorders in Pregnancy
Hypertensive disorders of pregnancy encompass a spectrum of conditions. According to the American College of Obstetricians and Gynecologists (ACOG) and international guidelines, they are classified as follows:
Classification | Definition | Key Features |
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Chronic Hypertension | Hypertension that predates pregnancy or is diagnosed before 20 weeks gestation |
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Gestational Hypertension | New onset of hypertension after 20 weeks gestation without proteinuria or other systemic features |
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Preeclampsia | New-onset hypertension after 20 weeks gestation with proteinuria or end-organ dysfunction |
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Preeclampsia with severe features | Preeclampsia with one or more severe complications |
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Eclampsia | Preeclampsia with grand mal seizures not attributable to other causes |
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HELLP Syndrome | Variant of severe preeclampsia characterized by Hemolysis, Elevated Liver enzymes, and Low Platelets |
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Chronic Hypertension with Superimposed Preeclampsia | Chronic hypertension complicated by preeclampsia |
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Memory Aid: “CREEP-HELP”
To remember the classifications:
- Chronic Hypertension
- Gestational Hypertension
- Preeclampsia (mild or severe)
- Eclampsia
- HELLP Syndrome
- Preeclampsia superimposed on chronic hypertension
Risk Factors
Certain factors increase the risk of developing pregnancy-induced hypertension. Understanding these risk factors is essential for early identification and management of high-risk pregnancies.
Category | Risk Factors | Level of Risk |
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Demographic Factors |
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Moderate |
Obstetric History |
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High |
Medical Conditions |
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High |
Family History |
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Moderate |
Placental Factors |
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High |
Genetic Factors |
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Variable |
Risk Assessment Tool
Current guidelines recommend low-dose aspirin (81 mg daily) prophylaxis starting between 12-28 weeks and continuing until delivery for women with:
- One or more high-risk factors
- Two or more moderate risk factors
Early identification of high-risk women allows for appropriate preventive measures and vigilant monitoring.
Clinical Manifestations
Pregnancy-induced hypertension presents with a range of clinical manifestations that vary in severity based on the classification and progression of the disorder.
Cardinal Signs
- Hypertension: Blood pressure ≥140/90 mmHg on two occasions at least 4 hours apart
- Proteinuria: ≥300 mg in a 24-hour urine collection, protein/creatinine ratio ≥0.3, or dipstick reading of 1+ (if quantitative methods unavailable)
- Edema: While no longer a diagnostic criterion, edema (particularly in the face, hands, and around the eyes) is commonly observed
System-Specific Manifestations
Body System | Clinical Manifestations | Nursing Assessment Focus |
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Cardiovascular |
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Renal |
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Neurological |
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Hepatic |
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Hematologic |
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Pulmonary |
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Uteroplacental |
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Signs of Severe Preeclampsia
The presence of any of the following indicates severe preeclampsia:
- Blood pressure ≥160/110 mmHg on two occasions at least 4 hours apart
- Thrombocytopenia (platelets <100,000/µL)
- Impaired liver function (elevated transaminases >2x normal)
- Progressive renal insufficiency (serum creatinine >1.1 mg/dL or doubling of baseline)
- Pulmonary edema
- New-onset cerebral or visual disturbances
- Severe persistent right upper quadrant or epigastric pain unresponsive to medication
Memory Aid: “HELLP ME”
For severe features of preeclampsia:
- Hypertension (≥160/110 mmHg)
- Elevated liver enzymes
- Low platelets (<100,000/µL)
- Liver pain (RUQ/epigastric)
- Pulmonary edema
- Mental changes/headache
- Eye disturbances
Assessment and Diagnosis
Accurate diagnosis of pregnancy-induced hypertension requires comprehensive assessment and diagnostic testing. Nurses play a crucial role in collecting assessment data and facilitating diagnostic procedures.
Nursing Assessment
1. History Taking
- Complete obstetric history (gravida, para, previous pregnancy complications)
- Medical history (pre-existing conditions, medications)
- Family history (hypertension, preeclampsia, cardiovascular disease)
- Current pregnancy symptoms (headache, visual changes, epigastric pain)
- Timing of symptom onset
2. Physical Examination
- Blood pressure measurement: Use appropriate technique following these guidelines:
- Patient seated with back supported
- Arm at heart level
- Appropriate cuff size (bladder encircling 80% of arm)
- At least 5 minutes of rest before measurement
- Readings at least 4 hours apart
- Edema assessment: Check for pitting edema in face, hands, sacrum, and lower extremities
- Weight measurement: Document recent weight changes (gain of >2 lbs/week in 2nd trimester or >1 lb/week in 3rd trimester suggests fluid retention)
- Neurological assessment: Deep tendon reflexes (hyperreflexia), clonus, level of consciousness
- Abdominal examination: Right upper quadrant/epigastric tenderness, uterine size/fundal height
- Pulmonary assessment: Respiratory rate, effort, auscultate for crackles
3. Fetal Assessment
- Fetal heart rate monitoring
- Fetal movement assessment
- Fundal height measurement (to assess for intrauterine growth restriction)
Diagnostic Tests
Diagnostic Test | Purpose | Abnormal Findings in PIH | Nursing Considerations |
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Urinalysis | Screen for proteinuria |
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24-hour urine collection | Quantify proteinuria | ≥300 mg protein/24 hours |
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Complete blood count | Assess for hematologic changes |
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Comprehensive metabolic panel | Evaluate organ function |
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Coagulation studies | Assess for coagulopathy |
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LDH and peripheral blood smear | Evaluate for hemolysis |
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Ultrasound | Assess fetal growth and placental status |
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Doppler velocimetry | Assess uterine/umbilical blood flow |
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Non-stress test/Biophysical profile | Assess fetal well-being |
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Diagnostic Criteria for Preeclampsia (ACOG Guidelines)
Blood pressure ≥140/90 mmHg on two occasions at least 4 hours apart after 20 weeks gestation, and either:
- Proteinuria ≥300 mg/24 hours (or protein/creatinine ratio ≥0.3 or dipstick 1+ if quantitative methods unavailable)
- OR in the absence of proteinuria, new-onset hypertension with any of the following:
- Thrombocytopenia (platelets <100,000/µL)
- Renal insufficiency (serum creatinine >1.1 mg/dL or doubling from baseline)
- Impaired liver function (elevated transaminases >2x normal)
- Pulmonary edema
- Cerebral or visual symptoms
Nursing Management
Effective nursing management of pregnancy-induced hypertension is essential for optimizing maternal and fetal outcomes. The nursing care focuses on monitoring, interventions to prevent complications, and education.
Monitoring and Surveillance
Parameter | Frequency | Nursing Interventions |
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Blood Pressure |
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Urine Output |
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Neurological Status |
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Edema | Every shift |
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Fetal Status |
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Laboratory Values | As ordered, typically daily for severe PIH |
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Therapeutic Interventions
1. Blood Pressure Management
Medication | Dosage | Nursing Considerations |
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Labetalol |
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Hydralazine | IV: 5-10 mg q20-40min (max 20 mg) |
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Nifedipine |
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Methyldopa | 250-500 mg PO BID-TID (max 3g/day) |
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Important Note:
Blood pressure management goal in pregnancy:
- For severe hypertension: Lower BP to 140-150/90-100 mmHg
- Avoid rapid or excessive blood pressure reduction as it may compromise uteroplacental perfusion
ACE inhibitors, ARBs, and nitroprusside are contraindicated in pregnancy due to potential fetal harm.
2. Seizure Prevention and Management
Magnesium Sulfate is the drug of choice for seizure prophylaxis and management in preeclampsia and eclampsia.
Administration | Dosage | Nursing Monitoring |
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Loading Dose | 4-6 g IV over 15-20 minutes |
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Maintenance | 1-2 g/hour continuous IV infusion | |
For Active Seizure | Additional 2 g IV bolus over 3-5 minutes |
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Toxicity Antidote | Calcium gluconate 1 g IV over 3-5 minutes |
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Memory Aid: “MAGNESIUM Toxicity – 10-5-2-1”
- 10 mEq/L: Cardiac arrest
- 5 mEq/L: Loss of deep tendon reflexes
- 2 mEq/L: ECG changes
- 1 mEq/L: Therapeutic level for normal physiology
Remember: “Respiratory Rate, Reflexes, and Renal output” – The 3 R’s for monitoring magnesium sulfate therapy
3. Fluid and Electrolyte Management
- Maintain fluid balance with careful monitoring of intake and output
- IV fluid rate typically 80-125 mL/hour (avoid fluid overload)
- Monitor for signs of pulmonary edema (crackles, dyspnea, decreased O2 saturation)
- Maintain accurate fluid balance records
4. Position and Activity Modifications
- Promote left lateral position to enhance uterine blood flow and reduce pressure on vena cava
- Limited activity or modified bed rest may be prescribed (complete bed rest is no longer routinely recommended)
- Minimize environmental stimuli (low lighting, reduced noise)
5. Patient Education
- Explain the condition, its risks, and warning signs
- Teach self-monitoring techniques (blood pressure, fetal movement, symptom recognition)
- Provide information on dietary recommendations (moderate sodium restriction, adequate protein)
- Explain medication regimens, including side effects to report
- Stress the importance of follow-up appointments
Preventive Measures
Low-Dose Aspirin for High-Risk Women
- 81 mg aspirin daily started between 12-28 weeks gestation
- Continue until delivery
- Recommended for women with high risk factors:
- Previous preeclampsia
- Multifetal pregnancy
- Chronic hypertension
- Type 1 or 2 diabetes
- Renal disease
- Autoimmune disease (SLE, APS)
Delivery Considerations
The definitive treatment for preeclampsia is delivery of the fetus and placenta. Timing depends on:
- Gestational age
- Severity of maternal condition
- Fetal status
Clinical Scenario | Recommended Timing of Delivery |
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Preeclampsia with severe features |
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Preeclampsia without severe features |
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Gestational hypertension |
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Chronic hypertension |
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Eclampsia |
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Postpartum Care
- Continue monitoring for at least 72 hours postpartum, as risk for complications remains high
- Most severe complications (eclampsia, stroke, pulmonary edema) occur in the postpartum period
- Continue antihypertensive therapy as needed
- Modify medication if breastfeeding
- Educate about signs and symptoms to report after discharge
- Schedule close follow-up (within 7-10 days of discharge)
- Discuss contraception and risks for future pregnancies
Practice Point: Postpartum Vigilance
Up to 25% of eclamptic seizures occur postpartum, with most occurring within the first 48 hours. However, eclampsia can occur up to 6 weeks postpartum. Maintain high vigilance during this period, especially for women who had severe preeclampsia.
Complications
Pregnancy-induced hypertension can lead to serious complications affecting both the mother and fetus if not properly managed. Understanding these potential complications is essential for early recognition and intervention.
Maternal Complications
Complication | Clinical Presentation | Nursing Implications |
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Eclampsia |
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HELLP Syndrome |
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Placental Abruption |
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Pulmonary Edema |
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Acute Kidney Injury |
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Cerebral Hemorrhage |
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DIC (Disseminated Intravascular Coagulation) |
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Liver Rupture/Hematoma |
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Long-term Cardiovascular Risk |
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Fetal/Neonatal Complications
Complication | Clinical Presentation | Nursing Implications |
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Intrauterine Growth Restriction (IUGR) |
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Oligohydramnios |
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Preterm Birth |
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Perinatal Asphyxia |
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Fetal Demise |
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Long-term Effects |
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Critical Time Periods
The risk for complications remains elevated during specific time periods:
- At presentation: Risk for eclampsia, placental abruption, and fetal distress
- During labor and delivery: Risk for cerebral hemorrhage, placental abruption, and HELLP syndrome
- 24-48 hours postpartum: Peak risk for pulmonary edema and eclampsia
- Up to 6 weeks postpartum: Continued risk for hypertension and late eclampsia
Vigilant monitoring should continue throughout these periods.
Nursing Care Plans
Comprehensive nursing care plans for patients with pregnancy-induced hypertension address key nursing diagnoses and provide structured interventions to optimize maternal and fetal outcomes.
1. Risk for Decreased Cardiac Output
Assessment | Nursing Interventions | Rationale | Expected Outcomes |
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2. Risk for Injury (Maternal and Fetal)
Assessment | Nursing Interventions | Rationale | Expected Outcomes |
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3. Risk for Ineffective Tissue Perfusion
Assessment | Nursing Interventions | Rationale | Expected Outcomes |
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4. Deficient Knowledge
Assessment | Nursing Interventions | Rationale | Expected Outcomes |
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5. Anxiety
Assessment | Nursing Interventions | Rationale | Expected Outcomes |
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Memory Aids
These memory aids will help nursing students remember key aspects of pregnancy-induced hypertension.
The “5 P’s” of Preeclampsia Pathophysiology
- Placental dysfunction (poor placentation)
- Pressure elevation (hypertension)
- Proteinuria (renal involvement)
- Peripheral edema (fluid shifts)
- Platelet dysfunction (coagulation changes)
CLASP: Warning Signs for Severe Preeclampsia
- Cerebral symptoms (headache, visual disturbances)
- Liver involvement (RUQ pain, elevated enzymes)
- Altered kidney function (oliguria, proteinuria)
- Severe hypertension (≥160/110 mmHg)
- Platelet abnormalities (<100,000/µL)
“RIGHT SIDE”: Nursing Priorities for PIH
- Rest in left lateral position
- Input/output monitoring
- Gauge blood pressure regularly
- Hyperreflexia assessment
- Treat symptoms promptly
- Seizure prevention (magnesium sulfate)
- Inform about danger signs
- Delivery planning
- Evaluate fetal well-being
MAGNESIUM Monitoring: “The 3 R’s + B”
- Respiratory rate (>12/min)
- Reflexes (present)
- Renal function (urinary output >30 mL/hr)
- Blood levels (therapeutic: 4-7 mEq/L)
ABCS of PIH Management
- Assess blood pressure, protein, and edema
- Bed rest (modified activity) in left lateral position
- Calcium gluconate (antidote for magnesium toxicity)
- Seizure prevention with magnesium sulfate
HELLP Syndrome: Remember the Definition
- Hemolysis
- Elevated
- Liver enzymes
- Low
- Platelets
Best Practices & Updates
Nursing care for pregnancy-induced hypertension continues to evolve as new research emerges. Here are three key updates to current practice that all nursing students should be aware of:
1. Low-Dose Aspirin Prophylaxis
The American College of Obstetricians and Gynecologists (ACOG) now recommends daily low-dose aspirin (81 mg) for women at high risk of preeclampsia. This should be initiated between 12-28 weeks of gestation and continued until delivery.
Clinical Implications: Nurses should identify high-risk women early in pregnancy for aspirin prophylaxis and educate them about the importance of adherence. This intervention can reduce the risk of preeclampsia by 24% and the risk of preterm birth by 14%.
2. Revised Diagnostic Criteria for Preeclampsia
Current guidelines no longer require proteinuria for the diagnosis of preeclampsia. Hypertension after 20 weeks gestation with evidence of end-organ dysfunction (thrombocytopenia, renal insufficiency, liver involvement, pulmonary edema, cerebral symptoms) is sufficient for diagnosis.
Clinical Implications: Nurses should remain vigilant for signs of preeclampsia even in the absence of proteinuria. This change allows for earlier detection and management of atypical presentations of preeclampsia.
3. Extended Postpartum Monitoring
Recent evidence indicates that women with hypertensive disorders of pregnancy should be monitored for at least 72 hours postpartum, with extended follow-up for up to 12 weeks. The risk of complications, including eclampsia and stroke, extends well into the postpartum period.
Clinical Implications: Nurses should educate patients about the importance of postpartum follow-up and the need to report concerning symptoms. Blood pressure should be checked within 7-10 days postpartum for all women with hypertensive disorders, with earlier checks for those with severe features.
Evidence-Based Practices for PIH Management
- Blood Pressure Targets: Current evidence supports treatment of severe hypertension (≥160/110 mmHg) to reduce the risk of stroke and other complications. The goal is to maintain BP between 140-150/90-100 mmHg rather than normalization.
- Magnesium Sulfate Therapy: Remains the gold standard for seizure prophylaxis in preeclampsia with severe features. It reduces the risk of eclampsia by more than 50% compared to placebo.
- Delivery Timing: For preeclampsia with severe features, delivery after 34 weeks is recommended. For preeclampsia without severe features, delivery at 37 weeks optimizes maternal and neonatal outcomes.
- Modified Bed Rest: Complete bed rest is no longer routinely recommended due to increased risk of thromboembolism. Activity modification with periods of left lateral rest is preferred.
- Calcium Supplementation: In populations with low calcium intake, supplementation during pregnancy may reduce the risk of preeclampsia by up to 64%.
References
- American College of Obstetricians and Gynecologists. (2020). ACOG Practice Bulletin No. 222: Gestational hypertension and preeclampsia. Obstetrics & Gynecology, 135(6), e237-e260. https://doi.org/10.1097/AOG.0000000000003891
- American College of Obstetricians and Gynecologists. (2019). ACOG Practice Bulletin No. 203: Chronic hypertension in pregnancy. Obstetrics & Gynecology, 133(1), e26-e50. https://doi.org/10.1097/AOG.0000000000003021
- Braunthal, S., & Brateanu, A. (2019). Hypertension in pregnancy: Pathophysiology and treatment. SAGE Open Medicine, 7, 2050312119843700. https://doi.org/10.1177/2050312119843700
- Cheng-Chen, C., & Jen-Jiuan, L. (2021). Effects of a case management program for women with pregnancy-induced hypertension. Journal of Nursing Research, 29(5), e167. https://doi.org/10.1097/JNR.0000000000000476
- Granger, J. P., Alexander, B. T., Bennett, W. A., & Khalil, R. A. (2001). Pathophysiology of pregnancy-induced hypertension. American Journal of Hypertension, 14(S3), 178S-185S. https://doi.org/10.1016/S0895-7061(01)02086-6
- Magee, L. A., Pels, A., Helewa, M., Rey, E., von Dadelszen, P., & Canadian Hypertensive Disorders of Pregnancy Working Group. (2014). Diagnosis, evaluation, and management of the hypertensive disorders of pregnancy: Executive summary. Journal of Obstetrics and Gynaecology Canada, 36(5), 416-441. https://doi.org/10.1016/S1701-2163(15)30588-0
- Mol, B. W., Roberts, C. T., Thangaratinam, S., Magee, L. A., de Groot, C. J., & Hofmeyr, G. J. (2016). Pre-eclampsia. The Lancet, 387(10022), 999-1011. https://doi.org/10.1016/S0140-6736(15)00070-7
- Phipps, E. A., Thadhani, R., Benzing, T., & Karumanchi, S. A. (2019). Pre-eclampsia: Pathogenesis, novel diagnostics and therapies. Nature Reviews Nephrology, 15(5), 275-289. https://doi.org/10.1038/s41581-019-0119-6
- Ramos, J. G. L., Sass, N., & Costa, S. H. M. (2017). Preeclampsia. Revista Brasileira de Ginecologia e Obstetrícia, 39(9), 496-512. https://doi.org/10.1055/s-0037-1604471
- Rana, S., Lemoine, E., Granger, J. P., & Karumanchi, S. A. (2019). Preeclampsia: Pathophysiology, challenges, and perspectives. Circulation Research, 124(7), 1094-1112. https://doi.org/10.1161/CIRCRESAHA.118.313276