What is the Richmond Agitation‑Sedation Scale (RASS) and how is it used to assess consciousness in adult intensive‑care patients?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: February 23, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

What is RASS?

The Richmond Agitation-Sedation Scale (RASS) is a 10-point scale ranging from +4 (combative) to -5 (unarousable) that provides the most valid and reliable assessment of sedation depth and agitation in adult ICU patients. 1, 2

Scale Structure and Scoring

  • RASS uses discrete numerical scores from +4 to -5, with positive scores indicating agitation, zero indicating calm and alert, and negative scores indicating sedation 1, 2
  • The scale defines specific levels:
    • +4 = Combative (overtly combative or violent)
    • +3 = Very agitated (pulls or removes tubes/catheters, aggressive)
    • +2 = Agitated (frequent non-purposeful movement, fights ventilator)
    • +1 = Restless (anxious but movements not aggressive or vigorous)
    • 0 = Alert and calm
    • -1 = Drowsy (not fully alert, sustained awakening to voice)
    • -2 = Light sedation (briefly awakens to voice, eye contact <10 seconds)
    • -3 = Moderate sedation (movement or eye opening to voice, no eye contact)
    • -4 = Deep sedation (no response to voice, movement to physical stimulation)
    • -5 = Unarousable (no response to voice or physical stimulation) 1

Psychometric Properties and Validation

  • RASS demonstrates excellent inter-rater reliability (r = 0.956) across diverse ICU populations, including medical, surgical, cardiac surgery, coronary, and neuroscience ICUs 3, 2
  • The scale shows high correlation with visual analog scales (r = 0.93) and moderate-to-high correlation with objective measures like EEG and bispectral index 1, 4
  • RASS achieves superior inter-rater agreement (weighted κ = 0.879) compared to older scales like Ramsay (weighted κ = 0.449), making it more reliable for clinical decision-making 5
  • The scale maintains validity in both ventilated and non-ventilated patients, and in those with or without sedative medications 3

Clinical Application and Target Goals

  • The Society of Critical Care Medicine recommends targeting RASS -2 to 0 (light sedation to awake and calm) for most mechanically ventilated adult ICU patients, as this reduces duration of mechanical ventilation and ICU length of stay 1, 2, 4
  • RASS should be assessed at least every 4 hours per shift to guide sedation titration 1
  • When patients are under-sedated (RASS >0), assess and treat pain first using validated pain scales, then administer sedatives as needed, preferring non-benzodiazepines unless treating alcohol or benzodiazepine withdrawal 1, 2
  • When patients are over-sedated (RASS <-2), hold sedative medications immediately until target is reached, then restart at 50% of the previous dose 1, 2

Treatment Adjustment Algorithm Based on RASS

For RASS >0 (agitated):

  • Assess pain using BPS or CPOT for non-communicative patients 1
  • Treat pain with IV opioids first 1, 4
  • If agitation persists after adequate analgesia, administer sedatives (propofol or dexmedetomidine preferred over benzodiazepines) 1, 2

For RASS -2 to 0 (target range):

  • Continue current sedation strategy 1, 2
  • Reassess regularly to maintain this light sedation level 2

For RASS <-2 (over-sedated):

  • Stop sedative infusions immediately 1, 2
  • Wait until patient reaches RASS -2 to 0 1
  • Restart sedatives at 50% of prior dose 1, 2

For RASS -3 to -5 (deep sedation):

  • Reserve only for specific indications: severe ARDS with refractory patient-ventilator asynchrony, intracranial hypertension, status epilepticus, neuromuscular blockade requirement, or profound hemodynamic instability 2, 4
  • Reassess need for deep sedation daily 2, 4

Advantages Over Other Scales

  • RASS is described by ICU nurses as logical, easy to administer, and readily recalled, facilitating consistent bedside implementation 3, 6
  • The scale demonstrates excellent internal consistency (Cronbach α = 0.989) compared to Ramsay scale (α = 0.828) 5
  • RASS provides better discrimination between sedation levels than older instruments, enabling more precise titration of sedative medications 1, 2

Critical Pitfalls to Avoid

  • Never rely on objective brain function monitors (BIS, entropy, PSI) as the primary sedation assessment method in non-paralyzed patients, as they are inadequate substitutes for RASS scoring 2, 4
  • Never use RASS in neonates or infants under 2 months, as it lacks validation in this population and does not account for developmental differences in pain and sedation responses 7
  • Do not use daily sedation interruption as justification for maintaining deep sedation (RASS <-3) during the remainder of the day when not clinically indicated 4
  • Always assess and treat pain before escalating sedation for agitation, as pain is frequently the underlying cause of apparent agitation 2, 4
  • Avoid benzodiazepines as first-line sedatives unless specifically treating alcohol or benzodiazepine withdrawal, as they increase delirium risk and prolong mechanical ventilation 2, 4

Implementation Considerations

  • Formal education on why and how to use RASS is essential for successful implementation and consistent application across ICU staff 6, 8
  • Visual management tools and reminder cards improve compliance with RASS-based sedation protocols 6
  • RASS facilitates interprofessional communication by providing a standardized language for discussing sedation goals 8

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

RASS Score-Based Treatment Adjustment in ICU Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

The Richmond Agitation-Sedation Scale: validity and reliability in adult intensive care unit patients.

American journal of respiratory and critical care medicine, 2002

Guideline

Analgosedation and Light‑Sedation Strategy for Mechanically Ventilated Adults

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Sedation Assessment in Neonates and Adults

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Related Questions

How is RASS (Richmond Agitation-Sedation Scale) scoring used to manage sedation in intensive care settings?
How should sedoanalgesia (sedation and analgesia) be managed in a critically ill patient in the Intensive Care Unit (ICU) following a surgical procedure?
Can the Richmond Agitation-Sedation Scale (RASS) score be used in pediatric patients?
How is a patient's treatment plan adjusted based on their Richmond Agitation-Sedation Scale (RASS) score?
How is the Richmond Agitation Sedation Scale (RASS) used to manage sedation and agitation in intensive care settings?
What is the recommended initial subcutaneous dose of nicotinamide adenine dinucleotide (NAD+) for an adult patient without known contraindications?
Can the injectable romiplostim (Nplate) increase platelet count?
Can intravenous meropenem cause an increase in platelet count?
What is the Behavioral Pain Index (BPS) and how is it used to assess pain in patients unable to self‑report?
How is pre‑exposure prophylaxis (PrEP) for HIV evaluated and initiated, including eligibility criteria, baseline testing (fourth‑generation antigen/antibody test, estimated glomerular filtration rate, hepatitis B and C status, pregnancy status, CBC, lipid panel), medication options (Truvada (emtricitabine/tenofovir disoproxil fumarate), Descovy (emtricitabine/tenofovir alafenamide), Apretude (cabotegravir) and on‑demand 2‑1‑1 schedule), dosing regimens, and follow‑up monitoring?
In patients with hormone‑receptor‑positive breast cancer, when is serum estradiol measurement indicated and is routine monitoring required?

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.