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.
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
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Braxton Hicks contractions | Irregular, painless, no cervical change | CTG, cervical length |
| Urinary tract infection | Dysuria, frequency, suprapubic pain | Urine MC&S |
| Round ligament pain | Sharp unilateral groin pain with movement | Clinical |
| Placental abruption | Constant pain, vaginal bleeding, tender uterus | Clinical, USS |
| Appendicitis | RIF pain, guarding, fever | USS, surgical review |
| Renal colic | Colicky loin-to-groin pain | USS 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
| Gestation | Survival | Major Disability |
|---|---|---|
| 23 weeks | 30-40% | 40-50% |
| 24 weeks | 40-55% | 25-35% |
| 26 weeks | 75-80% | 15-20% |
| 28 weeks | 90-95% | 8-10% |
| 32 weeks | >95% | 2-3% |
| 34 weeks | >98% | <1% |
Key Trials
| Trial | Finding |
|---|---|
| ORACLE | Erythromycin in PPROM reduces neonatal morbidity |
| MagNET/ACTOMgSO4 | MgSO4 neuroprotection before 30 weeks |
| APOSTEL III | Nifedipine vs atosiban (similar efficacy) |