Guides management of preeclampsia, gestational diabetes, and other high-risk conditions with monitoring protocols. Use when managing high-risk pregnancies, monitoring preeclampsia, or managing GDM.
Guides management of preeclampsia, fetal growth restriction, preterm labor, and other high-risk conditions with evidence-based monitoring protocols and delivery timing per ACOG and SMFM guidelines.
Approximately 6–8% of pregnancies in the United States are classified as high-risk, requiring increased surveillance and often multidisciplinary co-management with Maternal-Fetal Medicine (MFM). Hypertensive disorders of pregnancy complicate 5–10% of pregnancies and remain a leading cause of maternal mortality worldwide. ACOG Practice Bulletin No. 222 (Gestational Hypertension and Preeclampsia) and SMFM guidance on antenatal surveillance define specific monitoring intervals, laboratory thresholds, and delivery timing criteria that must be followed precisely.
Failure to escalate care, missing laboratory trends, or delivering too early or too late results in preventable morbidity. This skill structures the management of common high-risk conditions with precise criteria, surveillance schedules, and delivery timing algorithms.
Per ACOG Practice Bulletin No. 222:
| Diagnosis | Criteria |
|---|---|
| Chronic HTN | BP ≥ 140/90 before 20 weeks or pre-existing diagnosis |
| Gestational HTN | BP ≥ 140/90 after 20 weeks without proteinuria or severe features |
| Preeclampsia without severe features | BP ≥ 140/90 after 20 weeks + proteinuria (≥ 300 mg/24 hr or P/C ratio ≥ 0.3) OR other end-organ criteria |
| Preeclampsia with severe features | Any of: BP ≥ 160/110 on two occasions 4 hrs apart, platelets < 100K, creatinine > 1.1 or doubling, liver transaminases ≥ 2× ULN, pulmonary edema, new-onset headache unresponsive to medication, visual disturbances |
| HELLP syndrome | Hemolysis (LDH ≥ 600, schistocytes, bilirubin ≥ 1.2), Elevated Liver enzymes (AST/ALT ≥ 2× ULN), Low Platelets (< 100K) |
| Eclampsia | Preeclampsia + new-onset seizures |
| Superimposed preeclampsia | Chronic HTN + new proteinuria or sudden worsening / new severe features after 20 weeks |
Treat within 30–60 minutes per ACOG Committee Opinion No. 767:
| Agent | Protocol |
|---|---|
| Labetalol IV | 20 mg → 40 mg → 80 mg (q10 min) |
| Hydralazine IV | 5 mg → 10 mg (q20 min) |
| Nifedipine PO | 10 mg → 20 mg (q20 min) |
Per SMFM guidance, classify FGR and determine surveillance:
| FGR Classification | Criteria | Surveillance |
|---|---|---|
| EFW < 10th percentile, normal Doppler | Isolated small for GA | Growth US q 3–4 weeks, weekly NST starting 32 weeks |
| EFW < 10th percentile, elevated UA S/D ratio | FGR with abnormal Doppler | Growth US q 2–3 weeks, twice-weekly NST, weekly Doppler |
| EFW < 3rd percentile | Severe FGR | Growth US q 2 weeks, twice-weekly BPP, serial Doppler |
| Absent end-diastolic flow in UA | — | Consider admission, daily BPP, deliver by 34 weeks |
| Reversed end-diastolic flow in UA | — | Admit, continuous monitoring, betamethasone, deliver by 32 weeks or sooner if deteriorating |
Delivery timing:
Short cervix (< 25 mm on transvaginal US before 24 weeks):
Active preterm labor (23 + 0 to 33 + 6 weeks):
| Condition | Recommended Delivery GA |
|---|---|
| Uncomplicated pregnancy | 39 + 0 to 40 + 6 |
| Gestational HTN | 37 + 0 (or upon diagnosis if ≥ 37 wks) |
| Preeclampsia without severe features | 37 + 0 |
| Preeclampsia with severe features | 34 + 0 (after steroids if possible) |
| Chronic HTN (controlled) | 38 + 0 to 39 + 0 |
| Chronic HTN (poorly controlled) | 36 + 0 to 37 + 0 |
| GDM — diet-controlled | 39 + 0 to 40 + 6 |
| GDM — medication-controlled | 39 + 0 |
| Pre-gestational DM (well-controlled) | 37 + 0 to 39 + 0 |
| FGR (isolated, normal Doppler) | 37 + 0 to 38 + 0 |
| Dichorionic-diamniotic twins | 38 + 0 |
| Monochorionic-diamniotic twins | 36 + 0 |
| Prior classical cesarean | 36 + 0 to 37 + 0 |
| Placenta previa | 36 + 0 to 37 + 0 |