top of page

Eduovisual

Pregnancy, Childbirth & Puerperium

Preterm labor: diagnosis and management

Clinical Overview and When to Suspect Preterm Labor

— Contractions without documented cervical change = "threatened preterm labor," not true PTL.

— Preterm birth subcategories: late preterm 34–36 6/7, moderate 32–33 6/7, very preterm 28–31 6/7, extremely preterm <28 weeks.

— Pregnant patient 20–36 weeks reporting menstrual-like cramping, low back pain, pelvic pressure, increased vaginal discharge, spotting, or rhythmic tightening.

— Vague symptoms are common; low threshold for evaluation because earliest tocolytic and corticosteroid window is the most impactful.

Prior spontaneous preterm birth (strongest modifiable predictor).

Short cervical length (<25 mm before 24 wk by TVUS).

— Multiple gestation, polyhydramnios, uterine anomalies (septate, bicornuate), prior cervical procedures (LEEP, cone).

— Infection: bacteriuria/UTI, BV, chorioamnionitis, periodontal disease, STIs.

— Short interpregnancy interval (<18 mo), tobacco/cocaine use, low BMI, Black race, age <18 or >35, late/no prenatal care.

Board pearl: The single strongest predictor of recurrent preterm birth is a prior spontaneous preterm delivery <37 weeks — this drives both progesterone prophylaxis and serial cervical length surveillance starting at 16 weeks.

Definition: Regular uterine contractions (≥4/20 min or ≥8/60 min) with cervical change (dilation ≥3 cm or effacement ≥80%) between 20 0/7 and 36 6/7 weeks gestation.
Epidemiology / burden: ~10% of US births are preterm; leading cause of neonatal mortality and long-term neurodevelopmental morbidity. Disproportionately affects Black patients — a recognized Step 3 health-equity association.
When to suspect in clinic or triage:
Risk factors (high-yield):
Step 3 management: Any pregnant patient 20–36 6/7 weeks presenting with contractions, leaking fluid, or bleeding should be sent directly to L&D triage, not the outpatient clinic — CCS clock should reflect immediate transfer rather than scheduling a same-week visit.
Solid White Background
Presentation Patterns and Key History

Rhythmic abdominal tightening every few minutes, sometimes painless.

Low, dull back pain that comes and goes — frequently mistaken for musculoskeletal.

Pelvic pressure ("baby feels like it's falling out").

Change in vaginal discharge: mucoid, watery, blood-tinged ("bloody show").

Menstrual-like cramping.

Gush or continuous leak of fluid → suspect PPROM (preterm premature rupture of membranes), changes management drastically.

Heavy bleeding → rule out abruption or previa before pelvic exam.

Fever, foul discharge, uterine tendernesschorioamnionitis, contraindicates tocolysis and mandates delivery.

Decreased fetal movement → assess fetal status before focusing on contractions.

— Exact GA by best obstetric dating (LMP confirmed by first-trimester US is most reliable).

— Parity, prior preterm births and GA at delivery, prior cesarean, cervical procedures.

— Current pregnancy: singleton vs multifetal, placental location, GBS status, prior cervical length, 17-OH progesterone or vaginal progesterone use.

— Prenatal labs: blood type/Rh, GBS, infection screen, glucose tolerance.

— Tobacco, cocaine, methamphetamine (vasoconstriction → abruption, PTL).

— Recent UTI symptoms, dental infection, recent intercourse, group B Strep history.

— Domestic violence screening — abdominal trauma is a Step 3 mandatory ask in any pregnant patient with new contractions or bleeding.

— Braxton-Hicks: irregular, non-progressive, relieved by hydration/position change, no cervical change.

— True PTL: regular, increasing in intensity and frequency, with cervical change.

Key distinction: Painless cervical dilation in the mid-trimester (16–24 wk) with bulging membranes and no contractions is cervical insufficiency, not preterm labor — management is emergency cerclage, not tocolysis.

Classic complaint cluster (often vague):
Red-flag overlays to elicit on history:
Targeted OB history:
Substance, social, and infection history:
Distinguish from Braxton-Hicks:
Solid White Background
Physical Exam Findings (and Maternal-Fetal Assessment)

Vitals (maternal HR, BP, temp, RR, SpO2) — tachycardia + fever raises concern for chorioamnionitis or sepsis.

Continuous external fetal monitoring (EFM) + tocodynamometer — quantify contraction frequency, duration, fetal HR baseline and variability.

Leopold maneuvers for fetal lie/presentation.

Sterile speculum exam BEFORE digital exam if PPROM possible.

— Inspect for pooling of amniotic fluid in posterior fornix.

Nitrazine test: amniotic fluid turns paper blue (pH >6.5).

Ferning on dried slide under microscope.

— Inspect cervix visually for dilation, effacement, bleeding, prolapsed cord, or visible membranes.

— Obtain GBS, gonorrhea/chlamydia, and wet mount swabs if not recent.

— Document dilation (cm), effacement (%), station (–3 to +3), consistency, position.

— In PPROM, digital exams increase infection risk and should be deferred unless delivery is imminent.

Fundal height to corroborate GA.

Uterine tenderness → think abruption or chorioamnionitis.

Tense, board-like uterus with vaginal bleeding → placental abruption until proven otherwise.

— Reassuring: baseline 110–160, moderate variability, accelerations, no late/recurrent variable decels.

— Non-reassuring tracing in PTL workup escalates urgency toward delivery rather than tocolysis.

CCS pearl: On a CCS case of suspected preterm labor, your first three orders should be continuous fetal monitoring, IV access with crystalloid bolus, and sterile speculum exambefore labs return, before tocolytics, and before any digital exam if rupture is on the differential.

Initial L&D triage sequence (CCS-friendly order):
Speculum exam (high yield):
Digital cervical exam — only after PPROM is excluded:
Abdominal exam:
Fetal assessment:
Solid White Background
Diagnostic Workup — Initial Labs, Imaging, Biomarkers

CBC (leukocytosis suggests infection; anemia changes resuscitation).

Urinalysis + urine culture — UTI/pyelonephritis is a classic preterm labor trigger.

Urine drug screen (cocaine/meth strongly associated with PTL and abruption).

GBS culture if not done within 5 weeks — drives intrapartum antibiotic prophylaxis.

Cervical/vaginal swabs: GC/CT, wet mount for BV/trich.

Type & screen, especially if Rh-negative or bleeding.

— Sterile speculum: pooling + nitrazine + ferning = clinical PROM.

— Equivocal cases: commercial immunoassays (PAMG-1/AmniSure, IGFBP-1/Actim PROM).

Avoid digital exams until rupture excluded.

CL <20 mm before 30 weeks → high probability of preterm delivery within 7 days.

CL ≥30 mm → very low likelihood; supports observation/discharge.

— CL 20–29 mm → consider fetal fibronectin to refine risk.

— Performed between 22 0/7 and 34 6/7 weeks, on intact membranes, no recent intercourse or digital exam (within 24 h).

High negative predictive value (~99%) for delivery within 7–14 days when negative.

— Positive fFN is less specific — use to rule out, not rule in.

— Confirm GA, fetal presentation, estimated fetal weight, amniotic fluid index, placental location, anomalies.

— Multiple gestation status (chorionicity already known ideally).

Board pearl: The combination of negative fFN + cervical length ≥30 mm gives a <2% chance of delivery within 7 days — a classic Step 3 "safe to discharge with close follow-up" stem.

Core lab panel on L&D arrival:
Confirm rupture of membranes (if suspected):
Transvaginal ultrasound — cervical length (TVUS CL):
Fetal fibronectin (fFN):
Obstetric ultrasound:
Solid White Background
Diagnostic Workup — Advanced or Confirmatory Studies

— Indicated when clinical chorioamnionitis is uncertain but suspected (e.g., PPROM with maternal tachycardia but no fever).

— Send fluid for Gram stain, glucose (<14 mg/dL suggests infection), WBC, culture, and lactate.

— A positive result mandates delivery, not continued expectant management.

Renal/pelvic ultrasound if pyelonephritis suspected (hydronephrosis, stones).

Right upper quadrant ultrasound if abdominal pain mimics cholecystitis or HELLP.

MRI without contrast preferred over CT for non-OB abdominal pathology when feasible.

— BMP, LFTs, uric acid, LDH, haptoglobin, peripheral smear, urine protein/creatinine ratio or 24-h urine, platelet count.

— Rule out HELLP as a delivery indication masquerading as PTL.

— Fibrinogen <200 mg/dL in pregnancy is abnormal and points to DIC/abruption.

— Trends matter; a shortening cervix on serial TVUS in a high-risk patient supports admission and intervention even with equivocal contractions.

— If status unknown and delivery looks imminent, intrapartum PCR can guide antibiotic prophylaxis.

— In extreme prematurity (<26 wk), confirm absence of lethal anomalies before committing to aggressive resuscitation plans — informs counseling with neonatology.

Key distinction: Clinical chorioamnionitis (Triple I) is a clinical diagnosis — maternal fever ≥39.0 °C alone, or ≥38.0 °C plus fetal tachycardia, maternal leukocytosis, or purulent cervical discharge. Once diagnosed, delivery + broad-spectrum antibiotics is the rule regardless of GA; tocolysis is contraindicated.

Amniocentesis for suspected intraamniotic infection:
Imaging in atypical presentations:
Preeclampsia workup if BP elevated or symptoms overlap:
Coagulation studies and fibrinogen if bleeding or abruption suspected:
Repeat cervical length and fFN:
GBS rapid PCR:
Fetal anatomic re-evaluation:
Solid White Background
Risk Stratification and First-Line Management Logic

— Regular contractions + cervical change or + short CL or + positive fFN with symptoms → admit.

— Contractions without cervical change, CL ≥30 mm, negative fFN → observe 4–6 h, reassess, discharge with precautions.

Contraindications to tocolysis: chorioamnionitis, non-reassuring fetal status, severe preeclampsia/eclampsia, significant abruption with maternal/fetal instability, lethal fetal anomaly, intrauterine fetal demise, advanced labor (≥4 cm dilation often), GA ≥34 weeks (relative).

— Otherwise, the goal is to buy 48 hours for corticosteroid effect and maternal transfer.

<24 weeks: Counsel with neonatology re: periviability; individualize resuscitation; corticosteroids from 22 0/7 if active resuscitation planned.

24 0/7–33 6/7 weeks: Betamethasone, tocolysis ×48 h, MgSO4 for neuroprotection <32 wk, GBS prophylaxis if indicated.

34 0/7–36 6/7 weeks (late preterm): Single course of betamethasone if no prior course and delivery likely within 7 days; tocolysis generally not recommended.

≥37 weeks: No longer preterm; manage as term labor.

— If current facility lacks appropriate NICU level for the GA, arrange maternal transport while stable — safer than neonatal transport after birth.

Step 3 management: For a patient at 30 weeks in confirmed PTL, your "core bundle" orders are: (1) IM betamethasone 12 mg q24h ×2, (2) IV magnesium sulfate for neuroprotection, (3) tocolytic for 48 h, (4) GBS prophylaxis per status, (5) NICU and neonatology consult, (6) maternal transfer if not at a Level III facility.

Decision node #1 — Is this true preterm labor?
Decision node #2 — Is delivery contraindicated to delay?
Decision node #3 — Gestational age dictates bundle:
Decision node #4 — Transfer:
Solid White Background
Pharmacotherapy — First-Line Regimens

Betamethasone 12 mg IM q24h ×2 doses (preferred) or dexamethasone 6 mg IM q12h ×4.

— Indicated 24 0/7–33 6/7 weeks at risk of delivery within 7 days; considered from 22 0/7 if resuscitation planned.

Late preterm (34 0/7–36 6/7): single course if no prior course and delivery expected within 7 days — reduces neonatal respiratory morbidity.

Rescue course: one additional course if >14 days since first course, before 34 wk, and delivery again likely within 7 days.

— Benefits: ↓ RDS, IVH, NEC, neonatal death.

<32 weeks and delivery anticipated within 24 h.

— Typical: 4–6 g IV load over 20–30 min, then 1–2 g/h, usually for up to 12–24 h.

— Reduces cerebral palsy risk. Monitor DTRs, respirations, urine output, magnesium level; calcium gluconate is the antidote for toxicity.

Nifedipine (CCB) — first line for most; 20–30 mg PO load then 10–20 mg q4–6h. Avoid with hypotension; do not combine with magnesium (risk of profound hypotension/neuromuscular blockade).

Indomethacin (NSAID) — preferred <32 weeks; 50–100 mg load then 25–50 mg q4–6h. Avoid >32 wk (premature ductus closure, oligohydramnios). Limit to 48 h.

Terbutaline (β-agonist) — SC 0.25 mg; black-box: no prolonged use, no oral terbutaline (maternal cardiac events, death). Short-term tocolysis only.

Atosiban (oxytocin antagonist) — not FDA-approved in US.

Penicillin G IV (or ampicillin); cefazolin for low-risk penicillin allergy; clindamycin/vancomycin by susceptibility for anaphylaxis-risk allergy.

Board pearl: Tocolytics do not improve neonatal outcomes by themselves — their job is to buy 48 hours so corticosteroids and magnesium can work, and to allow transport to a facility with appropriate NICU level.

Antenatal corticosteroids (the single highest-yield intervention):
Magnesium sulfate for fetal neuroprotection:
Tocolytics (choose ONE, for ≤48 h):
GBS intrapartum prophylaxis:
Solid White Background
Procedures and Advanced Management

History-indicated cerclage (12–14 wk): ≥1 prior second-trimester loss attributed to painless cervical dilation, or prior cerclage.

Ultrasound-indicated cerclage (before 24 wk): singleton, prior spontaneous preterm birth <34 wk, and CL <25 mm on TVUS.

Exam-indicated ("rescue") cerclage: painless dilation with visible/bulging membranes <24 wk, no infection, no labor.

Contraindications: active labor, chorioamnionitis, PPROM, significant bleeding, lethal anomaly, IUFD.

— Cerclage is not effective in multiple gestations and may be harmful.

Vertex preterm singleton: vaginal delivery preferred when feasible.

Preterm breech, especially <32 wk: cesarean generally preferred due to head-entrapment risk and limited evidence for vaginal preterm breech.

Periviable (<25 wk): mode individualized; cesarean only if maternal indication or after explicit decision for active neonatal resuscitation, given maternal morbidity risk.

— Recommended in vigorous preterm neonates; ↓ IVH, transfusion need.

— Antenatal consult to counsel on survival/morbidity by GA, document shared decision-making.

— Confirm NICU bed availability before tocolysis fails or transfer window closes.

CCS pearl: For periviable PTL (22–25 wk), order a formal neonatology consult and document parental counseling about resuscitation goals before committing to cesarean for fetal indications — this is both an ethics and exam expectation on Step 3.

Cervical cerclage (procedural prevention, not acute PTL treatment):
Pessary: Limited US evidence; not routinely recommended.
Amnioinfusion: Considered for variable decels from cord compression in labor, not for PTL itself.
Mode of delivery considerations:
Delayed cord clamping (30–60 sec):
Neonatology and NICU coordination:
Solid White Background
Special Populations — Comorbid Maternal Disease

Avoid β-agonist tocolytics (terbutaline) in maternal arrhythmia, hyperthyroidism, severe hypertension; risk of pulmonary edema, MI.

Nifedipine preferred but watch BP in cardiac patients; avoid concurrent magnesium.

— Peripartum cardiomyopathy and pulmonary edema risk rises with tocolytics + corticosteroids + IV fluids — limit crystalloid to ~125 mL/h.

Magnesium clears renally → toxicity risk with CrCl <30; reduce maintenance dose, follow Mg levels q6h, monitor DTRs and respirations.

NSAIDs (indomethacin) worsen renal function and BP — avoid in preeclampsia or renal disease.

— Tocolysis generally contraindicated; delivery is the treatment.

— Steroids still given for fetal lung maturity if GA <34 wk and delivery not imminent within hours.

— Betamethasone causes transient hyperglycemia for 3–5 days; anticipate insulin requirement increases.

— Use sliding-scale or insulin infusion in poorly controlled cases.

— Indomethacin generally fine; avoid in aspirin-sensitive asthma.

— Terbutaline can worsen tachycardia but is bronchodilatory.

— Pyelonephritis, appendicitis, periodontal infection — treat the source; uterine activity often resolves.

— Suspected chorioamnionitis → deliver, no tocolysis.

— Cocaine/meth: rule out abruption; tocolysis after stabilization.

— Opioid use disorder: continue methadone or buprenorphine; do not abruptly taper.

Key distinction: Magnesium toxicity order — loss of DTRs first (~9–12 mg/dL), then respiratory depression (~12–18), then cardiac arrest (>25). Stop infusion, give calcium gluconate 1 g IV, support ventilation.

Cardiac disease:
Renal impairment / preeclampsia:
Hepatic dysfunction / HELLP:
Diabetes (pregestational or gestational):
Asthma:
Infections:
Substance use disorder:
Solid White Background
Special Populations — Multiples, Adolescents, and Periviable

— Twins and higher-order multiples account for a disproportionate share of PTL; median GA at delivery ~36 wk for twins, ~32 wk for triplets.

17-OH progesterone and cerclage are NOT effective in multifetal pregnancies for prevention.

Vaginal progesterone may be considered with short cervix in twins (evolving evidence).

— Magnesium neuroprotection and antenatal steroids: same indications by GA.

— Higher baseline PTL risk; also at risk for poor prenatal care attendance.

— Step 3 ethical layer: minors can usually consent to their own prenatal and labor care in most US states without parental consent (state-specific); document.

— Higher rates of comorbidities (HTN, DM) drive iatrogenic preterm delivery more than spontaneous PTL.

— Begin vaginal progesterone (200 mg suppository nightly) or — where still used — 17-OH progesterone caproate in selected patients starting 16 weeks (note: 17-OHPC has been withdrawn from US market; vaginal progesterone is current default).

Serial TVUS cervical lengths every 1–2 wk from 16 to 24 wk.

— Decision framework: antenatal steroids, MgSO4, tocolysis, cesarean for fetal indication, active neonatal resuscitation — each is optional and contingent on shared decision-making.

— Survival without major morbidity rises sharply each week: ~30% at 23 wk → >70% at 25 wk in modern NICUs.

Expectant management with latency antibiotics: ampicillin + azithromycin IV ×48 h, then amoxicillin PO ×5 d.

— Steroids, MgSO4 if <32 wk, no tocolysis after 34 wk.

Board pearl: 17-OH progesterone caproate (Makena) was withdrawn from the US market in 2023 after the PROLONG trial failed to confirm benefit — current first-line prevention for recurrent spontaneous PTL is vaginal progesterone in singletons with prior PTB or short cervix.

Multiple gestation:
Adolescent pregnancy (<18 yr):
Advanced maternal age (≥35 yr):
Prior preterm birth:
Periviable PTL (22 0/7–25 6/7 wk):
PPROM <34 weeks (no infection, no labor):
Solid White Background
Complications and Adverse Outcomes

Respiratory distress syndrome (RDS) — surfactant deficiency; mitigated by antenatal steroids.

Intraventricular hemorrhage (IVH) — especially <32 wk; reduced by steroids, MgSO4, delayed cord clamping.

Necrotizing enterocolitis (NEC) — favored by formula feeding; human milk protective.

Retinopathy of prematurity (ROP) — driven by oxygen exposure and immaturity; screening per AAP.

Bronchopulmonary dysplasia (BPD) — chronic oxygen need at 36 wk PMA.

Sepsis (early-onset GBS, E. coli) — empiric ampicillin + gentamicin.

Hypoglycemia, hypothermia, hyperbilirubinemia, feeding intolerance.

Long-term: cerebral palsy, developmental delay, learning disabilities, vision/hearing impairment.

Tocolytic adverse events: pulmonary edema (β-agonists, especially with fluid overload), hypotension (nifedipine), maternal arrhythmia (terbutaline), platelet dysfunction and renal effects (indomethacin).

Magnesium toxicity: loss of DTRs, respiratory depression, cardiac arrest — antidote calcium gluconate.

Chorioamnionitis → endometritis, sepsis, postpartum hemorrhage (atony in infected uterus).

Iatrogenic preterm cesarean morbidity: hemorrhage, infection, implications for future placentation (accreta).

— NICU separation, postpartum depression risk doubles with preterm birth — screen at every postpartum visit with Edinburgh or PHQ-9.

— Preterm birth accounts for the largest single share of newborn hospitalization costs in the US.

Step 3 management: A patient on magnesium + nifedipine who develops dyspnea and crackles is presenting with pulmonary edema — stop both agents, give supplemental O2, IV furosemide, sit upright, check Mg level, obtain CXR/ECG, and consider switching tocolytic class.

Neonatal complications (rise sharply with decreasing GA):
Maternal complications:
Psychosocial complications:
Healthcare system burden:
Solid White Background
When to Escalate Care — ICU, Consult, Transfer

— Magnesium toxicity with respiratory compromise.

— Pulmonary edema from tocolytics + fluids.

— Septic shock from chorioamnionitis or pyelonephritis.

— HELLP with hepatic hematoma, DIC, or AKI.

— Massive abruption with hemorrhagic shock and DIC.

— Periviable PTL (22–25 wk).

— Multiple gestation in PTL.

— Suspected accreta or anomalous placentation.

— Recurrent or refractory PTL despite tocolysis.

— Complex maternal disease (cardiac, renal transplant, lupus, sickle cell).

— Any expected delivery <34 wk.

— Anomalous fetus.

— Documented shared decision-making for periviable resuscitation.

— Default rule: transfer mother before delivery if local NICU level is insufficient.

Level I: well-newborn nursery.

Level II: ≥32 wk and ≥1500 g.

Level III: <32 wk or <1500 g, requires sustained ventilatory support.

Level IV: subspecialty surgical neonatal care.

— Admit: confirmed PTL with cervical change, PPROM, abruption, infection, non-reassuring tracing.

— Discharge with close follow-up (24–72 h): contractions resolved, no cervical change, CL ≥30 mm and/or fFN negative, reassuring fetal status, reliable patient and access to care.

CCS pearl: On a CCS case, ordering "transfer to tertiary-care center with Level III NICU" for a 27-week PTL patient before her cervix dilates to 6 cm is rewarded; waiting until she is in advanced labor and the baby must transfer postnatally is penalized for delayed disposition.

Escalate to OB-anesthesia and OB-intensivist / MICU:
Maternal-fetal medicine (MFM) consult:
Neonatology consult — antenatal, not after delivery:
Maternal transfer (in utero):
Inpatient vs outpatient triage:
Solid White Background
Key Differentials — Same-Category (Obstetric) Causes

— Irregular, non-progressive, painless or mildly uncomfortable, no cervical change. Resolve with hydration and rest. Reassurance + return precautions.

Painless cervical dilation in the second trimester, often with bulging membranes; no or minimal contractions.

— Management: emergency or history-/US-indicated cerclage, not tocolysis.

— Rupture without labor. Pooling, ferning, nitrazine positive.

— Management: latency antibiotics, steroids, MgSO4 <32 wk, deliver at 34 wk or sooner for infection/non-reassuring status.

— Painful vaginal bleeding, tense/tender uterus, frequent low-amplitude contractions, possible non-reassuring tracing, ± DIC.

— Cocaine, trauma, HTN, prior abruption are risks. Management: stabilize, deliver if maternal/fetal compromise.

Painless bleeding; previa diagnosed on US; vasa previa presents with bleeding at rupture with fetal bradycardia.

No digital exam until placenta location confirmed.

— Fever, fetal/maternal tachycardia, uterine tenderness, leukocytosis. Deliver + broad-spectrum antibiotics (ampicillin + gentamicin ± clindamycin for cesarean).

— Sharp, lateralized lower abdominal pain with movement; no contractions, no cervical change.

— Recheck GA dating — a misdated pregnancy at "35 weeks" may actually be 38 wk; tocolysis is inappropriate.

Key distinction: Painful contractions with bleeding + rigid uterus = abruption (clinical diagnosis; ultrasound often misses it); painless bleeding without contractions = previa (US confirms). Both are bleeding emergencies but the management priorities diverge.

Braxton-Hicks contractions:
Cervical insufficiency:
Preterm PROM (PPROM):
Placental abruption:
Placenta previa / vasa previa:
Chorioamnionitis / intraamniotic infection:
Round ligament pain:
Term labor mistaken for preterm:
Solid White Background
Key Differentials — Non-Obstetric Causes of Abdominal/Pelvic Pain

Cystitis / pyelonephritis — dysuria, frequency, CVA tenderness, fever; pyelo is a major PTL trigger. Treat with IV ceftriaxone until afebrile 24–48 h, then PO; avoid nitrofurantoin near term and sulfa in third trimester.

Nephrolithiasis — flank pain radiating to groin; renal/pelvic US, then low-dose CT if needed.

Appendicitis — pain often higher and more lateral in pregnancy as uterus displaces appendix; MRI preferred imaging if US non-diagnostic. Surgical emergency.

Cholecystitis / cholelithiasis — RUQ pain, Murphy sign, US-diagnosed; laparoscopic cholecystectomy can be done in any trimester (second trimester ideal).

Constipation, gastroenteritis, GERD — common pregnancy-related GI complaints, no cervical change.

HELLP, AFLP, intrahepatic cholestasis of pregnancy — RUQ pain, elevated LFTs, ± pruritus.

Round ligament pain, symphysis pubis dysfunction, sciatica.

Herpes zoster, shingles dermatomal pain mistaken for visceral.

Ovarian torsion — sudden, severe unilateral pain ± nausea; Doppler US. Often requires laparoscopy.

Degenerating fibroid — focal uterine tenderness, low-grade fever, conservative management with acetaminophen ± short NSAID course.

Pulmonary embolism — pregnancy is hypercoagulable; dyspnea, tachycardia. Workup: CXR → lower-extremity Doppler → V/Q or CTPA. Anticoagulate with LMWH.

Board pearl: A pregnant patient with fever, flank pain, and "contractions" is pyelonephritis until proven otherwise — treat the infection aggressively, and the contractions often resolve without tocolytics.

Urinary tract:
GI:
Hepatic:
MSK / dermatologic:
Adnexal:
Pulmonary / cardiac:
Solid White Background
Secondary Prevention and Long-Term Plan

— Document the index PTL details: GA at delivery, suspected etiology (infection, abruption, idiopathic, iatrogenic), cervical length history, prior interventions.

— Counsel: recurrence risk ~15–30% after one prior spontaneous PTL; higher with earlier index delivery and short interpregnancy interval.

— Recommend ≥18 months between delivery and next conception; <6 months doubles PTL risk.

— Discuss contraception before discharge — LARC (IUD, implant) ideal; postplacental IUD if available.

Singleton with prior spontaneous PTB <37 wkvaginal progesterone 200 mg nightly from 16 to 36 wk; serial TVUS cervical lengths every 1–2 wk from 16 to 24 wk.

Short CL <25 mm before 24 wk → vaginal progesterone (with or without prior PTB).

Prior PTB + short CL → consider cerclage.

17-OHPC is no longer used in the US.

— Smoking cessation (counseling + nicotine replacement if needed).

— Treat BV and asymptomatic bacteriuria, periodontal care.

— Optimize maternal nutrition, BMI, glycemic control, BP.

— Address substance use disorders (referral, MAT for OUD).

— Screen and treat STIs preconceptionally.

— Preterm birth (and preeclampsia) confer increased lifetime cardiovascular risk — counsel about long-term BP, lipid, glucose surveillance and lifestyle modification.

— Ensure NICU graduate clinic, audiology, ophthalmology (ROP), and early-intervention referrals are in place before discharge.

Step 3 management: At the 6-week postpartum visit after preterm delivery, your "secondary prevention" order set includes: contraception (LARC preferred), depression screen, BP check, glycemic follow-up if gestational DM, plan for vaginal progesterone in any future pregnancy from 16 wk, and smoking-cessation counseling.

Postpartum to next-pregnancy planning:
Interpregnancy interval:
Pharmacologic prophylaxis in next pregnancy:
Modifiable risk reduction:
Maternal long-term health:
Neonatal follow-up:
Solid White Background
Follow-Up, Monitoring, and Counseling

— Continuous EFM + toco during active intervention; intermittent thereafter if stable.

MgSO4 monitoring: DTRs hourly, respirations, urine output (≥30 mL/h), Mg level if symptoms or renal impairment.

Glucose checks q4–6 h × 3–5 days after betamethasone, especially in DM.

— Daily CBC, temperature curve in PPROM; vigilance for chorioamnionitis.

— Twice-weekly NST/BPP after 32 wk in stable PPROM.

— Follow-up within 3–7 days with OB; immediate return for new bleeding, leaking fluid, regular contractions, fever, decreased fetal movement.

— Activity modification individualized; strict bed rest is NOT recommended (no benefit, ↑ VTE risk).

— Continue vaginal progesterone if indicated.

— Serial TVUS cervical lengths every 1–2 wk from 16 to 24 wk.

— Growth ultrasounds q3–4 wk in third trimester if growth restriction concerns.

Influenza, Tdap (27–36 wk), COVID-19, RSV (32–36 wk) vaccinations on schedule.

— Fetal kick counts after 28 wk.

— Recognition of preterm labor symptoms.

— Contraindication of smoking, illicit drugs, alcohol.

— Mental health: anticipate NICU stress, postpartum depression screening.

— Document discussions about mode of delivery, neonatal resuscitation thresholds (especially periviable), breastfeeding plans, postpartum contraception.

Board pearl: Bed rest does not prevent preterm birth and may worsen outcomes via VTE, deconditioning, and depression — recommending it on a Step 3 stem is a distractor; the correct answer is targeted progesterone, cerclage when indicated, and treatment of modifiable risks.

Monitoring on inpatient PTL admission:
Discharge after stabilized non-progressive PTL:
Outpatient surveillance in high-risk patients:
Counseling priorities:
Birth plan and shared decision-making:
Solid White Background
Ethical, Legal, and Patient Safety Considerations

— Between 22 0/7 and 25 6/7 wk, decisions about antenatal steroids, MgSO4, cesarean for fetal indication, and active neonatal resuscitation should be made with explicit informed consent that reflects realistic survival and morbidity data.

— Document shared decision-making notes including survival statistics, expected NICU course, and parental values; revisit if conditions change.

— Respect parental refusal of cesarean for fetal indication at periviable GA — maternal autonomy is paramount.

Minor pregnant patient: in most US states, pregnant minors can consent to care related to their pregnancy and their newborn without parental involvement — but practices vary by state; consult risk management.

Patient with substance intoxication or altered capacity: if delivery is emergent and capacity is impaired, follow emergency exception to consent; involve surrogate when feasible.

Intimate partner violence (IPV) during pregnancy: routine screening; offer resources but reporting to law enforcement generally requires patient consent (state-specific).

Positive maternal/neonatal toxicology: many states mandate child welfare notification; know local law and document supportive interventions, not just punitive reporting.

Maternal in-utero transfer is safer than neonatal transfer — failing to transfer in time is a recurring sentinel-event theme.

Tocolytic + magnesium combinations are high-risk; standardized order sets, paired smart pumps, and bedside Mg toxicity protocols reduce errors.

Look-alike/sound-alike risk: betamethasone vs dexamethasone dosing schedules differ; verify.

— Black patients have ~50% higher preterm birth rates than white patients; this is largely driven by structural racism, not biology. Step 3 may test recognition of this disparity and the duty to address it through equitable care models.

Key distinction: Maternal autonomy generally supersedes fetal interests in US law — even a competent pregnant patient refusing a recommended cesarean for fetal indications must have that decision respected, with rigorous informed-consent documentation.

Periviable counseling and shared decision-making:
Informed consent edge cases:
Mandatory reporting:
Patient safety / transitions of care:
Health-equity:
Solid White Background
High-Yield Associations and Rapid-Fire Clinical Facts

Board pearl: If a Step 3 stem shows you a stable patient at 30 wk with regular contractions and 2 cm dilation, the single best next step is usually IM betamethasone — even before you choose a tocolytic, because steroids are what actually improve outcomes.

Strongest predictor of recurrent spontaneous preterm birth = prior spontaneous preterm birth.
Cervical length <25 mm before 24 wk = elevated PTL risk in singletons.
Fetal fibronectin negative + CL ≥30 mm = <2% delivery within 7 days.
Antenatal corticosteroids reduce RDS, IVH, NEC, and neonatal death — the single highest-impact intervention.
Magnesium sulfate <32 wk = fetal neuroprotection against cerebral palsy.
Tocolysis duration = up to 48 h, just enough for steroid effect.
Indomethacin = preferred tocolytic <32 wk; avoid >32 wk (premature ductal closure).
Nifedipine = preferred tocolytic for most patients; never combine with magnesium (synergistic hypotension/neuromuscular blockade).
Terbutaline = SC only, short-term; black-box against oral or prolonged use.
17-OH progesterone caproate (Makena) = withdrawn from US market; current prevention is vaginal progesterone.
Cerclage = singleton, prior PTB, CL <25 mm; not effective in twins.
PPROM <34 wk antibiotics = ampicillin + azithromycin IV ×48 h → amoxicillin PO ×5 d.
Chorioamnionitis = deliver; no tocolysis; antibiotics (ampicillin + gentamicin).
Late preterm (34–36 6/7 wk) steroids = single course if no prior course and delivery within 7 days.
Bed rest = no benefit, possible harm; not recommended.
GBS prophylaxis = penicillin first-line; cefazolin for low-risk allergy; clindamycin/vancomycin for high-risk allergy.
Maternal in-utero transfer > neonatal transfer when NICU level inadequate.
Smoking cessation is the single biggest modifiable lifestyle intervention.
Black race / structural racism = major contributor to US PTB disparity.
Delayed cord clamping 30–60 sec improves preterm neonatal outcomes.
Solid White Background
Board Question Stem Patterns

— 28-wk patient with cramping, CL 32 mm, fFN negative, no cervical change after 4 h observation. Next step: discharge home with OB follow-up in 3–7 days — not admission or tocolysis.

— Preeclamptic patient on MgSO4 develops loss of DTRs and RR 8. Next step: stop magnesium, give calcium gluconate 1 g IV, support ventilation, check Mg level.

— 28-wk PTL, no contraindications. Best tocolytic: indomethacin (preferred <32 wk).

— 33-wk PTL. Best tocolytic: nifedipine (avoid indomethacin >32 wk).

— 35-wk patient likely to deliver in 48 h, no prior steroid course. Next step: single course of betamethasone, no tocolysis, no MgSO4.

— Fever, fetal tachycardia, uterine tenderness, contractions. Next step: delivery + ampicillin + gentamicin, not tocolysis.

— Multipara with prior spontaneous PTB at 32 wk now at 14 wk. Next step: start vaginal progesterone at 16 wk and serial TVUS cervical lengths from 16–24 wk.

— 23-wk patient in PTL. Best next step: neonatology consult and shared decision-making about active resuscitation before committing to delivery mode.

— Fever, CVA tenderness, contractions. Next step: IV ceftriaxone, IV fluids, monitor — contractions usually resolve.

— Patient on MgSO4 receives nifedipine and becomes hypotensive. Cause: synergistic hypotension/NM blockade; avoid combination.

Step 3 management: Whenever the stem says "most likely to improve neonatal outcome," the answer is almost always antenatal corticosteroids — not the tocolytic, not the antibiotic, not the cerclage.

Stem 1 — "Negative fFN, long cervix":
Stem 2 — "Magnesium toxicity":
Stem 3 — "Tocolytic choice by GA":
Stem 4 — "Late preterm steroids":
Stem 5 — "Chorioamnionitis masquerading as PTL":
Stem 6 — "Recurrent PTL prevention":
Stem 7 — "Periviable counseling":
Stem 8 — "Pyelonephritis triggering PTL":
Stem 9 — "Drug interaction":
Solid White Background
One-Line Recap

Preterm labor — defined as regular contractions with cervical change between 20 0/7 and 36 6/7 weeks — is managed by confirming the diagnosis (cervical exam, TVUS cervical length, fetal fibronectin), then deploying the evidence-based bundle of antenatal corticosteroids, magnesium sulfate for neuroprotection if <32 weeks, a 48-hour tocolytic to buy time, GBS prophylaxis, and in-utero transfer to an appropriate-level facility — while ruling out chorioamnionitis, abruption, and PPROM that mandate delivery instead of delay.

Board pearl: When in doubt on a Step 3 PTL stem, your highest-yield single order is betamethasone, followed by magnesium sulfate (if <32 wk) and maternal in-utero transfer to a Level III center — these three move the needle on neonatal outcomes far more than any tocolytic choice ever will.

Highest-impact intervention = antenatal betamethasone (24 0/7–33 6/7 wk; single course also 34 0/7–36 6/7 wk if delivery within 7 d and no prior course).
Tocolytics buy 48 hours, no more — choose indomethacin <32 wk, nifedipine ≥32 wk, never combine nifedipine with magnesium.
Magnesium <32 wk = fetal neuroprotection; watch for toxicity (loss of DTRs → respiratory depression); antidote = calcium gluconate.
Prevention in next pregnancy = vaginal progesterone (200 mg nightly from 16 wk) for prior spontaneous PTB or short cervix; cerclage for prior PTB + CL <25 mm in singleton; 17-OHPC is off the US market.
Always rule out infection, abruption, and PPROM — these change management from "delay" to "deliver."
Solid White Background
bottom of page