🧠 Post-Cardiac-Arrest Neuroprognostication
Multimodal neuroprognostication for comatose survivors of cardiac arrest, requiring concordant unfavorable indicators after a defined delay.
Premature assessment (< 72 h or with sedation/hypothermia confounders) is unreliable and risks inappropriate withdrawal of care (original synthesis · not guideline verbatim).
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When to use
Use ≥ 72 h after ROSC, with confounders excluded, to combine clinical, electrophysiologic, biomarker, and imaging indicators.
How it works
At ≥ 72 h in a comatose patient (M ≤ 3), ≥ 2 concordant unfavorable indicators (absent pupillary/corneal reflexes, absent bilateral N20, malignant EEG, NSE > 60, status myoclonus, diffuse anoxic injury on CT/MRI) suggest poor prognosis; no single indicator decides.
Key points
- Premature assessment (< 72 h or with sedation/hypothermia confounders) is unreliable and risks inappropriate withdrawal of care (original synthesis · not guideline verbatim).
- A single positive indicator is insufficient; at least two concordant findings plus multidisciplinary consensus are required.
- Absent motor response or the GCS-M item alone has a high false-positive rate and must not determine prognosis.
References
- Nolan JP, et al. ERC-ESICM post-resuscitation care guidelines. Intensive Care Med 2021.
- Sandroni C, et al. Neuroprognostication after cardiac arrest. Intensive Care Med 2022.
Worked calculation
The values below come from this tool's own example placeholders and are computed server-side with the formula shown on this page, so the arithmetic can be checked quickly. It demonstrates how to substitute values only — it is not clinical advice and not a real case.
| Assessment timing | ≥ 72 h after ROSC, with sedation/paralysis/hypothermia and other confounders excluded |
|---|---|
| Bilateral pupillary + corneal reflexes absent (≥ 72 h) | No |
| Bilateral N20 (SSEP) absent | No |
| Highly malignant EEG (> 24 h, suppression/burst-suppression) | No |
| NSE > 60 µg/L (48 and/or 72 h) | No |
| Status myoclonus (≤ 72 h, early generalized) | No |
| CT/MRI diffuse extensive anoxic injury | No |
→NeuroprognosisNo poor-prognosis predictors (not equivalent to good prognosis)
- Positive indicators:0 → No poor-prognosis predictors (not equivalent to good prognosis)
- Decision rule:For a comatose patient (M ≤ 3) at ≥ 72 h, ≥ 2 concordant unfavorable indicators are required to suggest poor prognosis; no single indicator decides alone. The result must reach multidisciplinary consensus and be combined with clinical context
- Reliable indicators:Bilateral pupillary + corneal reflexes absent ≥ 72 h, bilateral N20 absent, highly malignant EEG > 24 h, NSE > 60 (a rising trend is more supportive), status myoclonus ≤ 72 h, CT/MRI diffuse anoxic injury
| Assessment timing | < 72 h or confounders still present |
|---|---|
| Bilateral pupillary + corneal reflexes absent (≥ 72 h) | Yes |
| Bilateral N20 (SSEP) absent | Yes |
| Highly malignant EEG (> 24 h, suppression/burst-suppression) | Yes |
| NSE > 60 µg/L (48 and/or 72 h) | Yes |
| Status myoclonus (≤ 72 h, early generalized) | Yes |
| CT/MRI diffuse extensive anoxic injury | Yes |
→NeuroprognosisDefer (timing not reached/confounders present)
- Principle:Reliable prognostication should be performed ≥ 72 h after ROSC, with sedation/paralysis/hypothermia/metabolic confounders excluded; premature assessment is unreliable — avoid premature withdrawal of life-sustaining therapy (WLST)
- Current positive indicators:6 (for reference only; no conclusion before the assessment window)
- Basis:ERC-ESICM 2021/2025 neuroprognostication guidelines; AHA 2020
Frequently asked questions
- What is Post-Cardiac-Arrest Neuroprognostication?
- Multimodal neuroprognostication for comatose survivors of cardiac arrest, requiring concordant unfavorable indicators after a defined delay.
- How is Post-Cardiac-Arrest Neuroprognostication calculated? What is the core formula?
- At ≥ 72 h in a comatose patient (M ≤ 3), ≥ 2 concordant unfavorable indicators (absent pupillary/corneal reflexes, absent bilateral N20, malignant EEG, NSE > 60, status myoclonus, diffuse anoxic injury on CT/MRI) suggest poor prognosis; no single indicator decides.
- When is Post-Cardiac-Arrest Neuroprognostication used?
- Use ≥ 72 h after ROSC, with confounders excluded, to combine clinical, electrophysiologic, biomarker, and imaging indicators.
- What are the key clinical points for Post-Cardiac-Arrest Neuroprognostication?
- Premature assessment (< 72 h or with sedation/hypothermia confounders) is unreliable and risks inappropriate withdrawal of care (original synthesis · not guideline verbatim). A single positive indicator is insufficient; at least two concordant findings plus multidisciplinary consensus are required. Absent motor response or the GCS-M item alone has a high false-positive rate and must not determine prognosis.
- What are the limits and cautions when using Post-Cardiac-Arrest Neuroprognostication?
- For licensed clinicians and clinical researchers. Interpret results with history, investigations and local protocols; not a diagnosis or prescription, and not a substitute for multidisciplinary decision-making or local guidelines.
- How is Post-Cardiac-Arrest Neuroprognostication calculated in practice? Can you show a worked example?
- Inputs: Assessment timing ≥ 72 h after ROSC, with sedation/paralysis/hypothermia and other confounders excluded, Bilateral pupillary + corneal reflexes absent (≥ 72 h) No, Bilateral N20 (SSEP) absent No, Highly malignant EEG (> 24 h, suppression/burst-suppression) No, NSE > 60 µg/L (48 and/or 72 h) No, Status myoclonus (≤ 72 h, early generalized) No, CT/MRI diffuse extensive anoxic injury No → Result: Neuroprognosis No poor-prognosis predictors (not equivalent to good prognosis)(Positive indicators: 0 → No poor-prognosis predictors (not equivalent to good prognosis), Decision rule: For a comatose patient (M ≤ 3) at ≥ 72 h, ≥ 2 concordant unfavorable indicators are required to suggest poor prognosis; no single indicator decides alone. The result must reach multidisciplinary consensus and be combined with clinical context, Reliable indicators: Bilateral pupillary + corneal reflexes absent ≥ 72 h, bilateral N20 absent, highly malignant EEG > 24 h, NSE > 60 (a rising trend is more supportive), status myoclonus ≤ 72 h, CT/MRI diffuse anoxic injury) Inputs: Assessment timing < 72 h or confounders still present, Bilateral pupillary + corneal reflexes absent (≥ 72 h) Yes, Bilateral N20 (SSEP) absent Yes, Highly malignant EEG (> 24 h, suppression/burst-suppression) Yes, NSE > 60 µg/L (48 and/or 72 h) Yes, Status myoclonus (≤ 72 h, early generalized) Yes, CT/MRI diffuse extensive anoxic injury Yes → Result: Neuroprognosis Defer (timing not reached/confounders present)(Principle: Reliable prognostication should be performed ≥ 72 h after ROSC, with sedation/paralysis/hypothermia/metabolic confounders excluded; premature assessment is unreliable — avoid premature withdrawal of life-sustaining therapy (WLST), Current positive indicators: 6 (for reference only; no conclusion before the assessment window), Basis: ERC-ESICM 2021/2025 neuroprognostication guidelines; AHA 2020)