MRI Safety Screening Protocol (ACR)
MRI Safety Screening Protocol (ACR): MRI Examination Ordered → Complete MRI Screening Form → Cardiac Device? → Proceed with EP Clearance.
Interactive Decision Tree
Algorithm Steps
- ▶Start
MRI Examination Ordered
- ●Action
Complete MRI Screening Form
Implants, devices, foreign bodies, pregnancy
- ◆Decision
Cardiac Device?
- MRI-Conditional
- MRI-Unsafe
- ■End
Proceed with EP Clearance
Device reprogrammed, monitoring
- ■End
MRI Contraindicated
Consider CT, US, nuclear
- ■End
No Contraindications
Proceed with examination
- ◆Decision
Other Implants?
- ●Action
Check MRIsafety.com
Verify device compatibility
- ■End
Proceed per Conditions
Follow SAR and field limits
- ◆Decision
Metallic Foreign Body?
- Orbital risk
- No risk
- ●Action
Orbit X-ray
Required if metalwork history
- ◆Decision
Pregnancy?
- ■End
MRI Generally Safe
Avoid gadolinium if possible
Guideline Source
ACR Guidance Document on MR Safe Practices
Clinical Safety Information
Clinical Decision Support — Not a Substitute for Clinical Judgment
Individual patient factors may require deviation from these recommendations.
Known Limitations
- Device databases not exhaustive
- New devices may lack safety data
- Field strength and SAR limits vary
Applicable Regions
UK: MHRA guidance
US: ACR guidance; mrisafety.com widely used
Next steps
Finish the workflow by opening the most relevant calculator, then convert the session into a live account when you are ready.
Related Resources
Frequently Asked Questions
What is the MRI Safety Screening Protocol (ACR)?
The MRI Safety Screening Protocol (ACR) is a diagnostic clinical algorithm for Radiology. It provides a structured decision tree to guide clinical decision-making, based on ACR Guidance Document on MR Safe Practices.
What guideline is the MRI Safety Screening Protocol (ACR) based on?
This algorithm is based on ACR Guidance Document on MR Safe Practices (DOI: 10.1002/jmri.26637).
What are the limitations of the MRI Safety Screening Protocol (ACR)?
Known limitations include: Device databases not exhaustive; New devices may lack safety data; Field strength and SAR limits vary. Individual patient factors may require deviation from these recommendations.
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