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) |