Preterm Labour

Preterm labour is the onset of regular uterine contractions with cervical change between 24+0 and 36+6 weeks gestation, the leading cause of neonatal morbidity and mortality worldwide.

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Key Facts

  • Preterm birth (<37 weeks) affects 7-8% of pregnancies in the UK
  • Prematurity is the leading cause of neonatal mortality and morbidity worldwide
  • Fetal fibronectin (fFN) and cervical length measurement are key diagnostic tools (NICE NG25)
  • Antenatal corticosteroids (betamethasone 12mg IM × 2) reduce RDS, IVH, and neonatal death if given 24-34+6 weeks
  • Magnesium sulphate for neuroprotection should be given if delivery expected <30 weeks (4g IV loading dose)
  • Nifedipine is first-line tocolytic in the UK (20mg PO loading, then 10-20mg TDS-QDS)
  • Cervical cerclage may be offered for cervical length <25mm on TVS before 24 weeks with history of preterm birth (NICE NG25)
  • Survival at 24 weeks is approximately 40-50%, rising to >95% at 32 weeks

Overview

Key Facts

Preterm labour is defined as the onset of regular painful uterine contractions leading to progressive cervical dilatation between 24+0 and 36+6 weeks of gestation. Preterm birth remains the leading cause of neonatal mortality and long-term disability.

Epidemiology

  • 7-8% of births in the UK are preterm
  • Approximately 60,000 preterm births per year in the UK
  • Spontaneous preterm labour accounts for 70-80% of preterm births
  • Iatrogenic preterm delivery (for maternal/fetal indication) accounts for 20-30%
  • Incidence has been relatively stable or slightly increasing due to assisted reproduction

Aetiology

  • Infection/inflammation (most common identifiable cause): chorioamnionitis, bacterial vaginosis, UTI
  • Cervical insufficiency
  • Uterine abnormalities (bicornuate uterus, fibroids)
  • Multiple pregnancy
  • Polyhydramnios
  • Previous preterm birth (strongest risk factor: recurrence risk 15-50%)
  • PPROM
  • Placental abruption
  • Social factors: smoking, low socioeconomic status, stress, domestic violence

Pathophysiology

  • Multiple pathways converge on activation of the myometrium and cervical ripening
  • Infection triggers inflammatory cascade (IL-1, IL-6, TNF-α) → prostaglandin production → uterine contractions
  • Premature activation of the hypothalamic-pituitary-adrenal axis
  • Cervical shortening and funnelling precede clinical labour
  • Decidual haemorrhage/abruption activates thrombin which stimulates contractions

Clinical Presentation

Symptoms

  • Regular, painful uterine contractions (≥4 in 20 minutes)
  • Lower abdominal cramping or pelvic pressure
  • Low back pain (constant or rhythmic)
  • Vaginal discharge (mucoid, bloody show)
  • Sensation of pelvic pressure or heaviness

Signs

  • Palpable regular uterine contractions on tocometry
  • Cervical dilatation and/or effacement on examination
  • Short cervical length on transvaginal ultrasound (<25mm is significant)

Red Flags

  • Cervical dilatation >3cm (advanced preterm labour - tocolysis unlikely to be effective)
  • Signs of chorioamnionitis (fever, tachycardia, uterine tenderness, offensive discharge)
  • Vaginal bleeding (abruption)
  • Abnormal CTG (fetal compromise)
  • PPROM (pooling of liquor on speculum)

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Braxton Hicks contractionsIrregular, painless, no cervical changeCTG, cervical length
Urinary tract infectionDysuria, frequency, suprapubic painUrine MC&S
Round ligament painSharp unilateral groin pain with movementClinical
Placental abruptionConstant pain, vaginal bleeding, tender uterusClinical, USS
AppendicitisRIF pain, guarding, feverUSS, surgical review
Renal colicColicky loin-to-groin painUSS KUB, urinalysis

Diagnosis / Investigation

Bedside

  • CTG (fetal monitoring)
  • Speculum examination (look for cervical dilatation, pooling of liquor, bleeding)
  • Fetal fibronectin (fFN) swab (if cervix <3cm dilated): negative result has >95% NPV for delivery within 7 days
  • Urinalysis and urine MC&S
  • Vital signs including temperature

Bloods

  • FBC, CRP (infection screen)
  • Blood cultures if pyrexial
  • Group and save
  • U&Es

Imaging

  • Transvaginal cervical length measurement: <25mm is significant, <15mm is high risk
  • Ultrasound for fetal presentation, weight estimation, liquor volume

Special Tests

  • High vaginal swab and low vaginal swab for Group B Streptococcus
  • Consider amniocentesis if infection suspected (rarely performed in UK practice)

Management

Non-pharmacological

  • Admit to unit with appropriate neonatal facilities
  • In utero transfer to tertiary unit if <27 weeks gestation
  • Neonatal team counselling regarding prognosis at given gestation
  • Bed rest (limited evidence but commonly advised)

Pharmacological

  • Antenatal corticosteroids: betamethasone 12mg IM × 2 doses (24 hours apart) if 24-34+6 weeks (NICE NG25). Single rescue course may be considered.
  • Tocolysis: nifedipine 20mg PO stat then 10-20mg TDS-QDS (first-line, NICE NG25). Used to gain 48 hours for steroid effect and in utero transfer.
  • Alternative tocolytic: atosiban (oxytocin receptor antagonist) 6.75mg IV bolus then infusion
  • Magnesium sulphate for neuroprotection: 4g IV loading dose over 15 minutes if delivery expected within 24 hours at <30 weeks (reduces risk of cerebral palsy by 30%)
  • Antibiotics: if evidence of infection (IV benzylpenicillin 3g then 1.5g 4-hourly for GBS prophylaxis)
  • Erythromycin 250mg QDS PO for 10 days if PPROM (ORACLE trial)

Surgical/Interventional

  • Cervical cerclage: rescue cerclage if cervical dilatation 1-4cm before 24 weeks with no infection (limited evidence)
  • Prophylactic cerclage at 12-14 weeks for women with history of ≥3 preterm births or second-trimester losses
  • Arabin pessary: alternative to cerclage (evidence debated)

Referral Criteria

  • All women in suspected preterm labour require hospital assessment
  • In utero transfer to tertiary unit if <27 weeks or anticipated neonatal surgical needs
  • Preterm birth prevention clinic referral for women with risk factors in subsequent pregnancies

Prognosis

  • Survival by gestational age: 24 weeks ~50%, 26 weeks ~75%, 28 weeks ~90%, 32 weeks ~95%, 34 weeks ~98%
  • Major morbidity (cerebral palsy, chronic lung disease, severe disability): 24 weeks ~30%, 28 weeks ~10%, 32 weeks ~3%
  • Antenatal corticosteroids reduce RDS by 34%, IVH by 46%, and neonatal death by 31%
  • Magnesium sulphate reduces cerebral palsy by 30% when given before 30 weeks
  • Recurrence risk of preterm birth: 15-50% (strongest predictor of subsequent preterm birth)

Other Relevant Information

Survival and Outcome by Gestational Age

GestationSurvivalMajor Disability
23 weeks30-40%40-50%
24 weeks40-55%25-35%
26 weeks75-80%15-20%
28 weeks90-95%8-10%
32 weeks>95%2-3%
34 weeks>98%<1%

Key Trials

TrialFinding
ORACLEErythromycin in PPROM reduces neonatal morbidity
MagNET/ACTOMgSO4MgSO4 neuroprotection before 30 weeks
APOSTEL IIINifedipine vs atosiban (similar efficacy)
Preterm Labour Revision Notes | MedPrep