11.2 Medical & Obstetric Complications of Pregnancy

Key Takeaways

  • Preeclampsia is diagnosed after 20 weeks gestation by BP ≥140/90 mmHg on two occasions at least 4 hours apart plus proteinuria (≥300 mg/24h or urine protein:creatinine ratio ≥0.3) or severe features (BP ≥160/110 mmHg, platelets <100,000/mcL, SCr >1.1 mg/dL, transaminases 2x normal, pulmonary edema, or cerebral/visual symptoms).
  • Intrapartum magnesium sulfate infusion (4-6 g IV loading dose followed by 1-2 g/h) is mandatory for seizure prophylaxis in preeclampsia with severe features and eclampsia; toxicity (loss of DTRs at 8-12 mEq/L, respiratory depression at 12-15 mEq/L) is reversed with 1 g intravenous calcium gluconate.
  • Gestational Diabetes Mellitus (GDM) screening at 24-28 weeks uses a 1-hour 50g glucose challenge test (threshold ≥130-140 mg/dL), followed by a diagnostic 3-hour 100g oral glucose tolerance test (GDM diagnosed if ≥2 values met: Fasting ≥95, 1-hr ≥180, 2-hr ≥155, 3-hr ≥140 mg/dL). First-line treatment is dietary modification and exercise; insulin is the preferred pharmacotherapy when glycemic targets (fasting <95 mg/dL, 2-hr postprandial <120 mg/dL) fail.
  • Medical management of unruptured ectopic pregnancy with methotrexate is indicated when the patient is hemodynamically stable, ectopic mass is <3.5 cm without fetal cardiac activity, baseline beta-hCG is <5,000 mIU/mL, and renal/hepatic function is normal.
  • Placenta previa presents as painless third-trimester vaginal bleeding and requires C-section delivery at 36 0/7 to 37 6/7 weeks; digital vaginal examination is strictly contraindicated prior to transvaginal ultrasound confirmation due to the risk of life-threatening hemorrhage.
Last updated: July 2026

Medical & Obstetric Complications of Pregnancy

Hypertensive Disorders of Pregnancy

Hypertensive disorders affect 5–10% of pregnancies and represent a leading cause of maternal and perinatal morbidity. Classification is based on gestational age at onset, presence of proteinuria, and organ-specific severe features:

  • Chronic Hypertension: Blood pressure ≥140/90 mmHg documented prior to pregnancy or before 20 weeks gestation, persisting >12 weeks postpartum.
  • Gestational Hypertension: New-onset BP ≥140/90 mmHg occurring after 20 weeks gestation in the absence of proteinuria or severe features. Resolves <12 weeks postpartum.
  • Preeclampsia: New-onset hypertension (≥140/90 mmHg on 2 readings at least 4 hours apart) after 20 weeks gestation accompanied by proteinuria (≥300 mg/24-hour urine collection, urine protein:creatinine ratio ≥0.3, or dipstick 2+).
  • Preeclampsia with Severe Features: Diagnosed when preeclampsia is accompanied by ANY of the following severe criteria (proteinuria is NOT required if severe features are present):
    • Severe blood pressure elevation: systolic ≥160 mmHg or diastolic ≥110 mmHg on two occasions at least 15 minutes apart
    • Thrombocytopenia: platelets <100,000/mcL
    • Impaired liver function: transaminases (AST/ALT) ≥2 times upper limit of normal or severe persistent right upper quadrant / epigastric pain
    • Progressive renal insufficiency: serum creatinine >1.1 mg/dL or doubling of baseline serum creatinine
    • Pulmonary edema
    • New-onset cerebral or visual disturbances (persistent severe frontal headache, scotomas, blurred vision)
  • Eclampsia: Development of new-onset tonic-clonic seizures in a patient with preeclampsia. Managed with IV magnesium sulfate, blood pressure stabilization, and emergency delivery.
  • HELLP Syndrome: A severe variant of preeclampsia defined by Hemolysis (microangiopathic hemolytic anemia with schistocytes, serum total bilirubin >1.2 mg/dL, and LDH >600 U/L), Elevated Liver enzymes (AST/ALT ≥2x upper limit of normal), and Low Platelets (<100,000/mcL). Carries high risk of hepatic subcapsular hematoma rupture, DIC, and placental abruption.

Prevention, Antihypertensives & Seizure Prophylaxis

  • Prophylaxis: Low-dose aspirin (81 mg/day) initiated between 12 and 16 weeks gestation for patients at high risk for preeclampsia (prior preeclampsia, multifetal gestation, chronic hypertension, pregestational diabetes, renal disease, autoimmune disease).
  • Acute Antihypertensive Therapy: Indicated for severe hypertension (BP ≥160/110 mmHg) to reduce stroke risk. First-line agents include:
    • Intravenous Labetalol: Combined alpha-1 and beta-blocker. Avoid if maternal bradycardia (<60 bpm) or severe asthma.
    • Intravenous Hydralazine: Direct vasodilator. Can cause reflex tachycardia and headache.
    • Oral Immediate-Release Nifedipine: Calcium channel blocker. Preferred if IV access is delayed.
    • Note: ACE inhibitors, ARBs, and direct renin inhibitors are strictly teratogenic (cause renal dysgenesis, oligohydramnios, skull hypoplasia) and contra-indicated in all trimesters.
  • Seizure Prophylaxis: Intravenous Magnesium Sulfate (MgSO4) is the agent of choice for seizure prevention in preeclampsia with severe features and for seizure treatment in eclampsia. Administered as a 4–6 g IV loading dose over 15–20 minutes followed by 1–2 g/hour continuous IV maintenance infusion for 24 hours postpartum.
    • Magnesium Toxicity Monitoring: Loss of deep tendon reflexes (patellar reflex) occurs at therapeutic levels of 4–7 mEq/L (loss of DTRs at 8–12 mEq/L; respiratory depression at 12–15 mEq/L; cardiac arrest at >15 mEq/L). Monitor hourly urine output (>30 mL/hr), respiratory rate (>12/min), and patellar reflexes.
    • Antidote for Magnesium Toxicity: Intravenous Calcium Gluconate (1 g IV over 2–5 minutes).
  • Timing of Delivery:
    • Preeclampsia without severe features: Delivery at 37 0/7 weeks gestation.
    • Preeclampsia with severe features / HELLP syndrome: Delivery at ≥34 0/7 weeks gestation (or immediately at any gestational age if maternal/fetal condition deteriorates, e.g., eclampsia, DIC, abruption, refractory severe BP).

Gestational Diabetes Mellitus (GDM)

Gestational diabetes arises from human placental lactogen (hPL / human chorionic somatomammotropin) inducing maternal insulin resistance in the 2nd and 3rd trimesters to ensure adequate glucose delivery to the fetus.

  • Screening & Diagnosis (2-Step Method at 24-28 weeks):
    • Step 1: 1-hour 50g Glucose Challenge Test (GCT). Serum glucose ≥130–140 mg/dL is positive.
    • Step 2: Diagnostic 3-hour 100g Oral Glucose Tolerance Test (OGTT) following an 8-12 hour fast. GDM is diagnosed if ≥2 values equal or exceed Carpenter-Coustan thresholds:
      • Fasting: ≥95 mg/dL
      • 1-Hour: ≥180 mg/dL
      • 2-Hour: ≥155 mg/dL
      • 3-Hour: ≥140 mg/dL
  • Management Protocols:
    • First-line: Nutritional modification (33-40% complex carbohydrates) and light exercise (30 mins post-meal walking).
    • Glycemic Targets: Fasting blood glucose <95 mg/dL, 1-hour postprandial <140 mg/dL, or 2-hour postprandial <120 mg/dL.
    • Pharmacotherapy: If glycemic targets are not achieved after 1–2 weeks of dietary modification, subcutaneous insulin is the first-line pharmacotherapy of choice (does not cross the placenta). Metformin and glyburide are second-line options.
  • Fetal & Neonatal Complications: Fetal hyperinsulinemia driven by maternal hyperglycemia leads to fetal macrosomia (EFW >4,500 g), shoulder dystocia, neonatal hypoglycemia (abrupt loss of maternal glucose supply post-delivery while fetal insulin remains high), polycythemia, hyperbilirubinemia, hypocalcemia, and delayed lung maturity (hyaline membrane disease).
  • Postpartum Management: Discontinue insulin immediately post-delivery. Perform a 2-hour 75g OGTT at 4–12 weeks postpartum to screen for persistent type 2 diabetes mellitus.

Early Pregnancy Loss & Ectopic Pregnancy

  • Ectopic Pregnancy: Implantation outside the endometrial cavity, most commonly in the ampulla of the fallopian tube (95%). Classic presentation: amenorrhea, lower abdominal pain, and vaginal bleeding.
    • Evaluation: Transvaginal ultrasound (TVUS) and quantitative serum beta-hCG. The beta-hCG discriminatory zone (1,500–2,000 mIU/mL) is the level at which an intrauterine gestational sac should reliably be visible on TVUS. An empty uterus with beta-hCG above the discriminatory zone strongly suggests ectopic pregnancy.
    • Medical Management (Methotrexate): Folic acid antagonist that inhibits DNA synthesis in rapidly dividing trophoblastic tissue. Indications for methotrexate:
      1. Hemodynamically stable patient with no severe abdominal pain
      2. Unruptured ectopic mass <3.5 cm in diameter
      3. No fetal cardiac activity on ultrasound
      4. Baseline serum beta-hCG <5,000 mIU/mL
      5. Normal baseline hepatic and renal function, and reliable patient follow-up
    • Surgical Management (Laparoscopic Salpingostomy / Salpingectomy): Indicated for hemodynamically unstable patients, signs of tubal rupture (peritonitis, hemoperitoneum), failed methotrexate therapy, or contraindications to methotrexate.
  • Spontaneous Abortion Subtypes: Defined as pregnancy loss prior to 20 weeks gestation.
    • Threatened Abortion: Vaginal bleeding, closed cervical os, fetal cardiac activity present on ultrasound.
    • Inevitable Abortion: Vaginal bleeding, cramping, open cervical os, products of conception visible at os or internal os dilated, no tissue passed yet.
    • Incomplete Abortion: Vaginal bleeding, severe cramping, open cervical os, partial passage of products of conception with retained tissue in uterus.
    • Complete Abortion: Vaginal bleeding/cramping resolved, closed cervical os, complete passage of all products of conception, empty uterine cavity on ultrasound.
    • Missed Abortion: Nonviable fetus retained in utero, closed cervical os, no vaginal bleeding or cramping.

Third-Trimester Hemorrhage & Placental Disorders

Third-trimester vaginal bleeding is an obstetric emergency requiring immediate maternal stabilization and fetal heart rate evaluation.

FeaturePlacenta PreviaPlacental Abruption (Abruptio Placentae)Vasa Previa
EtiologyPlacenta implants over internal cervical osPremature separation of placenta from decidua basalisFetal vessels course unprotected through membranes over internal os
Clinical PresentationPainless, bright red vaginal bleedingPainful, dark vaginal bleeding with severe uterine tendernessPainless bleeding occurring immediately upon rupture of membranes
Uterine ToneNormal, soft, non-tender uterusHypertonic, rigid, "woody", tender uterusNormal uterine tone
Fetal StatusReassuring unless maternal shock occursNon-reassuring (late decelerations, bradycardia)Rapid fetal bradycardia / sinusoidal tracing (fetal exsanguination)
Risk FactorsPrior C-section, multiparity, prior uterine surgeryMaternal hypertension, cocaine use, trauma, smokingSuccenturiate placenta, velamentous cord insertion, IVF
ContraindicationDigital vaginal exam strictly contraindicatedRapid vaginal exam delayed until previa excludedDigital exam contraindicated
ManagementScheduled C-section at 36 0/7–37 6/7 weeksEmergency C-section if fetal/maternal distressEmergency C-section immediately upon membrane rupture
              [ Suspected Preeclampsia (BP ≥140/90 mmHg after 20 weeks) ]
                                           |
               +---------------------------+---------------------------+
               |                                                       |
  [ Check Proteinuria & Severe Criteria ]                  [ Chronic Hypertension ]
   - Urine Protein ≥300 mg/24h or PCR ≥0.3                   (BP ≥140/90 pre-pregnancy
   - Severe BP ≥160/110 mmHg                                  or <20 weeks gestation)
   - Platelets <100,000/mcL
   - SCr >1.1 mg/dL or ALT/AST ≥2x normal
   - Pulmonary Edema or Cerebral/Visual Symptoms
               |
       +-------+-------+
       |               |
  [ Present ]     [ Absent ] ---> [ Gestational Hypertension ]
       |                               (BP ≥140/90, no proteinuria/severe features)
       v
[ Preeclampsia Confirmed ]
       |
       +-------------------------------+-------------------------------+
       |                                                               |
[ Any Severe Feature Present? ]                                 [ No Severe Features ]
 (BP ≥160/110, Platelets <100k,                                        |
  AST/ALT 2x, SCr >1.1, Headache/Scotomas)                             v
       |                                                [ Delivery at 37 0/7 Weeks ]
       +-------------------------------+
       | Yes                           | Eclampsia (Seizures) / HELLP
       v                               v
[ Preeclampsia with Severe Features ] [ Emergency Stabilization ]
       |
       |- 1. Antihypertensives for BP ≥160/110 (IV Labetalol, IV Hydralazine, Oral Nifedipine)
       |- 2. IV Magnesium Sulfate Loading (4–6 g IV) + Maintenance (1–2 g/hr) for Seizure Prophylaxis
       |- 3. Delivery at ≥34 0/7 Weeks (or immediate delivery if maternal/fetal decompensation)
Test Your Knowledge

A 34-year-old G2P1 woman at 33 weeks gestation presents to the emergency department with severe headache, right upper quadrant abdominal pain, and visual scotomas. Her blood pressure is 168/112 mmHg. Laboratory evaluation reveals hemoglobin 10.1 g/dL, platelets 68,000/mcL, AST 185 U/L, ALT 210 U/L, total bilirubin 1.8 mg/dL, and lactate dehydrogenase (LDH) 820 U/L. Peripheral blood smear shows schistocytes. What is the most appropriate definitive management for this patient?

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Test Your Knowledge

A 29-year-old G1P0 woman at 26 weeks gestation undergoes a 1-hour 50g glucose challenge test with a result of 158 mg/dL (normal <130 mg/dL). A follow-up 3-hour 100g oral glucose tolerance test (OGTT) yields the following results: Fasting 98 mg/dL (normal <95), 1-hour 188 mg/dL (normal <180), 2-hour 162 mg/dL (normal <155), 3-hour 132 mg/dL (normal <140). What is the initial first-line management for this condition?

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Test Your Knowledge

A 25-year-old G1P0 woman at 32 weeks gestation presents with sudden-onset, dark vaginal bleeding and severe continuous abdominal pain. She has a history of poorly controlled gestational hypertension and active cigarette smoking. On physical examination, her uterus is firm, hypertonic, and tender to palpation. Electronic fetal monitoring shows high-frequency, low-amplitude uterine contractions and recurrent late decelerations. What is the most likely diagnosis?

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