Here is a full summary of both documents, written to be clear and detailed at the same time.
Document 1: PhysioCTG 2018 - The Original Guideline
What it is: The first fetal monitoring guideline based entirely on physiology (understanding why the fetal heart rate changes) rather than just pattern recognition (describing what the trace looks like).
The Core Idea
Old guidelines classified CTG traces into categories (Normal / Suspicious / Pathological) by ticking boxes and combining features. This guideline argues that approach misses the point. Instead, you need to understand what is happening to the fetus physiologically - is it coping? Is it running out of reserves? Is it deteriorating?
The key question to always ask: "Is THIS fetus fit to undertake the progressive hypoxic journey of labour?"
CTG Features - The Basics
| Feature | Normal | Abnormal |
|---|
| Baseline rate | 110-160 bpm | <110 (bradycardia) or >160 (tachycardia) |
| Variability | 5-25 bpm bandwidth | <5 bpm (reduced) or >25 bpm (saltatory) |
| Accelerations | Present, >15 bpm rise, >15 sec | Absent |
| Cycling | Alternating sleep/wake states | Absent - sign of CNS compromise |
Cycling is particularly important - it means the fetal brain is switching between sleep and active states, which is a sign of normal neurological function. Loss of cycling is a red flag.
Saltatory pattern (variability >25 bpm) is associated with rapidly evolving hypoxia or autonomic instability. It needs urgent attention, especially in the second stage.
Sinusoidal pattern (smooth, regular sine-wave) suggests severe fetal anaemia (e.g. anti-D alloimmunisation, vasa praevia). It is a serious sign.
The Four Types of Hypoxia
This is the heart of the guideline. Hypoxia in labour follows one of these patterns:
1. Acute Hypoxia
- Looks like: A prolonged deceleration lasting >3 minutes (or >5 minutes)
- Caused by: The 3 major intrapartum accidents - cord prolapse, placental abruption, uterine rupture - OR iatrogenic causes: maternal hypotension, uterine hyperstimulation
- Key rule - the 3-Minute Rule:
- 0-3 min: Alarm raised, team called
- 3-6 min: Find the cause. If an accident - prepare immediate delivery. If iatrogenic - fix it (stop oxytocin, change position, give tocolytic)
- 6-9 min: Look for recovery (variability returning, heart rate stabilising)
- 9-12 min: If not recovering, delivery should be underway
- Important caveat: If the deceleration was preceded by reduced variability and absent cycling, skip the 3-minute rule - deliver immediately. If variability and cycling were normal before and in the first 3 minutes, 90% will recover by 6 min and 95% by 9 min.
2. Subacute Hypoxia
- Looks like: Fetus spending most of its time in decelerations - more time down than at the baseline
- Caused by: Uterine hyperstimulation (too many/too long contractions)
- pH drops at: 0.01 per 2-3 minutes (slower than acute)
- Management: Stop oxytocin/prostaglandins, change position, give tocolytic, consider delivery. In second stage, stop pushing first and see if it improves within 10 minutes.
3. Gradually Evolving Hypoxia (most common)
This follows a stepwise progression - like what happens to an athlete during sustained exercise:
- Decelerations appear (hypoxic stress)
- Accelerations disappear, cycling is lost
- Decelerations become wider and deeper
- Baseline rises - catecholamine surge, fetus trying to redistribute blood to vital organs (first sign of attempted compensation)
- Variability reduces - brain now vasoconstricting to protect itself (decompensation begins)
- Step-ladder pattern - unstable, progressively falling baseline (pre-terminal)
- Stages 1-4 = compensated - fetus is stressed but coping
- Stages 5-6 = decompensated - fetus is failing
- The goal is to intervene at stage 4 (rising baseline) before decompensation
4. Chronic Hypoxia (antenatal, affects labour care)
- Looks like: Baseline at upper end of normal, reduced variability, blunted or absent accelerations, absent cycling, shallow decelerations
- This fetus has already used up its reserves before labour even starts
- Very low threshold for intervention during labour
- Use the Chronic Hypoxia Checklist to screen for this at the start of monitoring
The Fetal Monitoring Checklist
Before starting intrapartum monitoring, assess:
- Is the baseline appropriate for gestational age?
- Is variability normal with cycling present?
- Are there true accelerations?
- Are there no shallow/late decelerations?
- Consider the clinical picture: meconium, temp, growth restriction, reduced movements
Overall impression: Normal / Chronic Hypoxia / Other
Intrapartum CTG Assessment Tool
At each review, ask:
- Has the baseline risen by ≥10%?
- Is the inter-contraction interval >90 seconds? (less than this = not enough recovery time between contractions)
- Is cycling maintained?
- Is variability abnormal (<5 or >25 bpm)?
- Are there features of hypoxia? If so, what type?
- Are central organs well oxygenated (stable baseline + normal variability)?
Intermittent Auscultation (IA)
For low-risk women, IA is appropriate. Method:
- Listen immediately after a contraction for at least 1 minute
- Every 15 minutes in first stage, every 5 minutes in active second stage
- Always palpate the maternal pulse simultaneously to avoid confusing it with the fetal heart
- Document as a single number, not a range
Switch to continuous CTG if: rising baseline, slow-recovering decelerations, persistent overshoots, maternal fever, meconium, hyperstimulation, epidural, or any risk factor (see full list in the document).
Adjunctive Tests
Fetal Scalp Stimulation (FSS):
- Rub the fetal scalp during a vaginal examination
- If an acceleration is provoked: risk of acidosis is <2.5%
- If no acceleration: risk of acidosis is >38%
STAN (ST analysis / Fetal ECG):
- Detects myocardial glycogenolysis (energy shortage in the heart) via ST segment changes
- Only useful with a stable baseline and normal variability at the start
- Ignore ST events on a normal CTG - they occur in 50% of well-oxygenated fetuses
- Do NOT use in: chorioamnionitis/sepsis, chronic hypoxia, pre-terminal traces, acute hypoxia, active second stage
- The guideline presents a cautious recommendation - STAN is potentially useful but must be used alongside clinical judgement
Fetal Scalp Blood Sampling (FBS):
- The 2013 Cochrane review found no benefit
- May actually increase caesarean section rates
- The authors do not recommend FBS in this guideline
What NOT to Do
- Maternal oxygen to a well-oxygenated mother does NOT help the fetus and may cause harm
- IV fluids in a normotensive, well-hydrated woman do NOT improve fetal oxygenation and give false reassurance
Special Circumstances (summary)
| Situation | Key Point |
|---|
| Meconium | Extra vigilance for hypoxia; lower threshold to deliver |
| Oxytocin | Stop if hyperstimulation; full assessment before restarting |
| Pyrexia | Increases fetal metabolic demand; pyrexia + acidosis = high risk of neonatal encephalopathy |
| Epidural | Can cause sudden maternal hypotension → acute deceleration |
| Scar rupture | May present as sudden acute bradycardia |
| Subclinical chorioamnionitis | Only 8-12% have fever - watch for rising baseline without preceding decelerations |
| Preterm | Higher baseline, less variability, fewer accelerations are normal for gestation |
Document 2: CTG Consensus 2024 - The Updated Guideline
What it is: A formal revision by an international panel of 44+ experts from 14 countries, updating the 2018 guideline with new scientific evidence. Published in the European Journal of Obstetrics & Gynecology (2024).
Why Was It Updated?
Since 2018, new evidence emerged on:
- The Zig-Zag pattern (a specific type of increased variability)
- Features of chorioamnionitis (infection/inflammation) on the CTG
- A new concept called RUPI-L (Relative Utero-Placental Insufficiency of Labour)
- Debate about the role of baroreceptors vs chemoreceptors in causing decelerations
- Evidence that units using physiological CTG interpretation had fewer emergency caesareans and less HIE (hypoxic-ischaemic encephalopathy)
Key Changes and New Concepts
1. New Deceleration Terminology - Away from "Early / Variable / Late"
The panel notes that deceleration morphology (shape, timing relative to contractions) has no proven correlation with poor perinatal outcomes. Therefore, they replaced baro/chemoreceptor terminology with two simple types based on likely cause:
"Quicklie" deceleration:
- Abrupt drop from baseline (>30 bpm), reaches nadir within 30 seconds, quick recovery
- Caused by umbilical cord compression - transient hypoxaemia only, not true hypoxia/acidosis
- What to assess: the intervening baseline between decelerations - is it stable with reassuring variability and cycling?
"Tardy" deceleration:
- Gradual drop, slow recovery even after the contraction has ended
- Caused by utero-placental insufficiency - can be associated with acidosis if variability is reduced
- Often due to structural placental damage (infarction, thrombosis) - cannot be reversed by position change or fluids
Practical tip: The panel still includes morphological types (early/variable/late) for clinicians not yet fully confident in physiological interpretation, but strongly encourages moving away from them over time.
2. The Zig-Zag Pattern - Renamed and Redefined
Previously called "saltatory pattern" (which required >25 bpm variability for >30 minutes). Problem: during labour, ongoing contractions mean you rarely see 30 minutes of uninterrupted increased variability.
New definition - Zig-Zag pattern:
- Abrupt, erratic up-and-down fluctuations in FHR variability >25 bpm
- Lasting at least 1 minute (much shorter threshold than "saltatory")
- Caused by autonomic instability - likely parasympathetic nervous system predominance during intense hypoxic stress
Why it matters - the evidence:
- Zig-Zag lasting >2 minutes = approximately 11-fold increase in neonatal unit admission
- Marked increased variability lasting >1 minute = 2-fold increase in neonatal acidosis
Management:
- Zig-Zag lasting >1 min: act immediately - reduce/stop oxytocin, consider tocolytic
- Zig-Zag during active pushing in second stage: stop directed pushing immediately to restore fetal cerebral oxygenation via carotid arteries
- Zig-Zag + rising baseline without repetitive decelerations: think fetal neuroinflammation from chorioamnionitis - avoid further hypoxic stress
3. SOFI - Suggestive of Fetal Inflammation (Chorioamnionitis)
New addition to the classification table. Recognises that only 8-12% of chorioamnionitis cases have obvious maternal fever and tachycardia - the rest are subclinical and detectable on the CTG.
CTG sign of SOFI:
- Baseline FHR increase of >10% without preceding repetitive decelerations (or baseline >10% higher than expected for gestational age)
Evidence base:
- IL-6 levels in umbilical artery at birth are 5-fold higher in fetuses with >10% baseline rise without decelerations
- Absence of cycling is associated with a 4-fold increase in maternal pyrexia
- When neuroinflammation features (absent cycling, Zig-Zag, sinusoidal) are present alongside SOFI, IL-6 levels are 4-fold higher still
- Fetuses with SOFI contributed to approximately 30% of all composite adverse outcomes
Features of neuroinflammation on CTG:
- Loss of cycling
- Zig-Zag pattern
- Sinusoidal pattern
Management: If neuroinflammation features are present - expedite birth. The concern is that adding hypoxic stress on top of an already inflamed fetal brain dramatically increases the risk of neonatal encephalopathy.
ChorioDuck Score: A recently published scoring system to help recognise chorioamnionitis on the CTG. A score >5 may help with clinical decisions, but more large-scale evidence is still needed before routine use is recommended.
4. RUPI-L - Relative Utero-Placental Insufficiency of Labour (New Concept)
The concept: Some fetuses have a subclinically impaired placenta that isn't bad enough to cause growth restriction or obvious antenatal CTG abnormalities - but is unmasked the moment regular uterine contractions begin, because contractions intermittently reduce placental blood flow.
CTG signs of RUPI-L (appear as soon as regular contractions start):
- Wide and deep decelerations immediately from the onset of regular contractions or induction
- Decelerations improve or disappear when contractions reduce in strength/frequency
- Baseline between decelerations often at the upper end of normal (due to chronic catecholamine release from long-standing subclinical hypoxia)
- Zig-Zag pattern episodes (1-10 minutes long)
Key point: These fetuses may look fine on an antenatal CTG but decompensate quickly in labour. The goal is to recognise RUPI-L early so you can modify stress or expedite birth.
5. Baroreceptor Debate Resolved (Practically)
Some animal researchers questioned whether baroreceptors cause decelerations, arguing chemoreceptors are dominant. The consensus panel's response: this academic debate is a distraction from clinical care. What matters is understanding the mechanism well enough to act. Therefore:
- References to "baroreceptor-mediated" and "chemoreceptor-mediated" decelerations have been removed from the updated guideline
- Replaced by the simpler Quicklie/Tardy classification (based on likely underlying cause - cord compression vs utero-placental insufficiency)
6. Updated Checklist Tools
Fetal Monitoring Checklist ("Is THIS fetus FIT for labour?") - updated to include:
- Signs of chorioamnionitis
- Signs of RUPI-L
Intrapartum Fetal Assessment Tool ("How is THIS fetus?") - updated to include:
- Initial baseline FHR (to make identifying a ≥10% rise easier)
- Recognition of hypoxic stress superimposed on ongoing fetal inflammation
7. Avoiding Erroneous Maternal Heart Rate Recording
"Double Mountain Peak Sign": Large-amplitude accelerations coinciding with uterine contractions suggest the machine is picking up the maternal heart rate rather than the fetal heart rate (because the maternal HR rises with contractions, while the fetal HR typically decelerates).
Other signs of erroneous recording: sudden apparent "improvement" in variability, sudden "disappearance" of decelerations, sudden drop or rise in the recorded baseline.
Action: Stop oxytocin and active pushing immediately until the true fetal heart rate is confirmed by maternal pulse oximetry, ultrasound, or fetal scalp electrode.
8. Things That Are NOT Recommended (confirmed/strengthened)
Fetal Scalp Blood Sampling (FBS) - now explicitly recommended against:
- Multiple Cochrane reviews (2007, 2013, 2017) found no improvement in long-term outcomes
- A 2019 UK multicentre study found FBS increased emergency caesarean section rates by 60%
- The Flamingo RCT (the only RCT directly comparing FBS to CTG alone) also showed no benefit
- Recommendation: FBS should no longer be used in clinical practice
STAN (Fetal ECG / ST analyser):
- A 2024 meta-analysis of all 9 RCTs on STAN found no benefit when used alongside the traditional "Normal/Intermediary/Abnormal" CTG table
- It may be beneficial if used alongside physiological CTG interpretation - but this is not yet confirmed
- Current recommendation: not recommended with the traditional table; to be reviewed once physiological CTG is more widely implemented
Maternal oxygen supplementation:
- Not recommended to correct FHR abnormalities in a well-oxygenated mother
- ACOG Practice Bulletin (2022) confirms this - routine oxygen use is not recommended for Category II/III traces
IV fluids to correct FHR abnormalities:
- Not recommended unless the mother is genuinely dehydrated, hypotensive, or septic
- NHS Resolution 2019 report: excess fluids in labour increase neonatal convulsions (dilutional hyponatraemia) and maternal/neonatal morbidity from fluid overload
Updated Classification Table (Summary)
| Type | CTG Features | Management |
|---|
| No Hypoxia | Appropriate baseline, normal variability, cycling, no repetitive decelerations | Routine hourly review |
| Chronic Hypoxia | Higher baseline than expected, reduced variability/absent cycling, absent accelerations, shallow decelerations | Avoid further stress; expedite delivery if not imminent |
| RUPI-L | Wide/deep decelerations from onset of contractions, Zig-Zag, upper-normal baseline | Consider clinical context; may need to expedite |
| Gradually Evolving - Compensated | Rising baseline (with normal variability), decelerations, loss of accelerations; inter-deceleration interval > time in deceleration | Conservative interventions; review every 30-60 min |
| Gradually Evolving - Decompensated | Reduced or increased variability (Zig-Zag), rising baseline, repetitive decelerations; step-ladder pattern | Urgent intervention (stop oxytocin/prostaglandins, tocolytic); expedite delivery if no improvement |
| Subacute Hypoxia | More time in decelerations (>90s) than at baseline (<30s); possible Zig-Zag | 1st stage: stop oxytocin, tocolysis, consider delivery within 10-15 min. 2nd stage: stop pushing, consider tocolysis or operative delivery |
| Acute Hypoxia | Prolonged deceleration >3 min | If preceded by reduced variability: deliver immediately. If preceded by normal variability and cycling: 3-minute rule applies |
| SOFI/Chorioamnionitis | >10% baseline rise without preceding decelerations ± loss of cycling / Zig-Zag / sinusoidal | Consider progress of labour and parity; if neuroinflammation features present, expedite birth |
| Other abnormal patterns | Double Mountain Peak sign, sinusoidal, uncertain baseline | Escalate; exclude maternal HR recording; exclude non-hypoxic causes (fetal anaemia, arrhythmia) |
How the Two Documents Relate
| PhysioCTG 2018 | CTG Consensus 2024 |
|---|
| Core framework | Types of hypoxia; compensation vs decompensation | Same framework, retained and expanded |
| Decelerations | Early / Variable / Late + physiological explanation | "Quicklie" / "Tardy" - cleaner, pathophysiology-based |
| Increased variability | "Saltatory pattern" (>30 min threshold) | "Zig-Zag pattern" (>1 min threshold - more practical) |
| Chorioamnionitis | Mentioned in special circumstances | Full entry in classification table with IL-6 evidence |
| RUPI-L | Not included | New concept - subclinical placental insufficiency unmasked by contractions |
| FBS | Not recommended | Explicitly recommended against (stronger wording) |
| Maternal oxygen/fluids | Not recommended | Not recommended - reinforced with ACOG bulletin |
| STAN | Cautiously supported | Not recommended with current CTG tables; to be reviewed |
The 2024 document states it replaces and supersedes the 2018 guideline, but the 2018 guideline must still be read alongside it to understand the foundational principles.