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radiology/SOPs/Imaging-Procedures/SOP-RAD-001-CT-Protocol.md

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Standard Operating Procedure: CT Imaging Protocol

Document ID SOP-RAD-001
Title Computed Tomography (CT) Imaging Protocol
Revision 1.0
Effective Date [DATE]
Author [AUTHOR]
Approved By [APPROVER]
Department Radiology/Diagnostic Imaging

1. Purpose

To establish standardized procedures for performing computed tomography (CT) examinations to ensure patient safety, optimal image quality, and regulatory compliance with ACR, state, and federal requirements.

2. Scope

This procedure applies to all CT examinations including:

  • Non-contrast CT studies
  • Contrast-enhanced CT studies
  • CT angiography (CTA)
  • CT-guided procedures
  • Emergency/trauma CT

3. Responsibilities

3.1 CT Technologist

  • Screen patients for contraindications
  • Position patient properly
  • Select and execute protocols
  • Assess image quality
  • Monitor patient during examination

3.2 Radiologist

  • Approve protocols
  • Supervise contrast administration
  • Interpret studies and generate reports
  • Manage contrast reactions

3.3 Radiology Nurse (if applicable)

  • Assess IV access
  • Administer contrast
  • Monitor for reactions
  • Provide patient care

3.4 Medical Physicist

  • Establish dose optimization protocols
  • Perform quality control
  • Monitor radiation exposure

4. Definitions

Term Definition
CTDI CT Dose Index - measure of radiation output
DLP Dose Length Product - total dose metric
HU Hounsfield Units - density measurement
kVp Kilovoltage peak
mAs Milliampere-seconds
MPR Multiplanar reconstruction

5. Equipment and Materials

  • CT scanner (accredited)
  • Power injector
  • Contrast media (iodinated)
  • IV supplies
  • Emergency equipment and medications
  • Shielding devices
  • Patient monitoring equipment

6. Procedure

6.1 Pre-Examination

6.1.1 Order Verification

  • Valid physician order present
  • Appropriate indication documented
  • Protocol selection appropriate for indication
  • Prior imaging reviewed (if available)

6.1.2 Patient Identification

  • Verify using two identifiers
  • Confirm exam matches order
  • Review clinical history

6.1.3 Safety Screening

For all patients:

  • Pregnancy status (women of childbearing age)
  • Previous CT studies (cumulative dose awareness)
  • Ability to cooperate with positioning
  • Metal implants/devices in scan field

For contrast studies - additional screening:

Risk Factor Check
Previous contrast reaction ☐ Yes ☐ No
Allergies (iodine, shellfish) ☐ Yes ☐ No
Kidney disease/elevated creatinine ☐ Yes ☐ No
Diabetes (metformin use) ☐ Yes ☐ No
Thyroid disease ☐ Yes ☐ No
Multiple myeloma ☐ Yes ☐ No
Age >70 years ☐ Yes ☐ No
Dehydration ☐ Yes ☐ No

Renal Function Assessment:

eGFR Level Risk Action
≥60 Low risk Proceed
45-59 Moderate risk Hydration, consider alternatives
30-44 High risk Alternative imaging preferred, radiologist approval
<30 Very high risk Avoid unless emergent, nephrology consult
  • Explain procedure and risks
  • Obtain informed consent for contrast (if applicable)
  • Document consent

6.2 Patient Preparation

6.2.1 Preparation by Exam Type

Exam Type Preparation Required
Head CT Remove metallic objects from head/neck
Chest CT Breathing instructions, arms above head
Abdomen/Pelvis CT Oral contrast (if ordered), full bladder (pelvic)
CT Angiography IV access, contrast protocol
CT Colonography Bowel preparation

6.2.2 IV Access for Contrast

  • Assess vein suitability
  • 20-gauge or larger preferred for power injection
  • Verify patency with saline flush
  • Secure catheter properly

6.3 Patient Positioning

6.3.1 Standard Positions

Body Part Position Gantry Entry
Head Supine, neutral Head first
Neck Supine, neck extended Head first
Chest Supine, arms up Head or feet first
Abdomen Supine, arms up Head first
Pelvis Supine, arms up Feet first
Extremity Per protocol Varies

6.3.2 Positioning Considerations

  • Center patient in gantry
  • Use positioning aids as needed
  • Apply shielding where appropriate
  • Ensure patient comfort
  • Remove all artifacts from scan field

6.4 Protocol Selection and Parameters

6.4.1 Dose Optimization Principles

  • ALARA (As Low As Reasonably Achievable)
  • Use automatic exposure control (AEC)
  • Size-appropriate protocols
  • Limit scan range to clinical question

6.4.2 Standard Protocol Parameters

Protocol kVp mAs Slice Thickness Pitch
Head routine 120 Auto 5mm N/A (axial)
Chest routine 120 Auto 5mm/1.25mm 1.0-1.5
Abdomen routine 120 Auto 5mm/2.5mm 1.0-1.5
CT Angiography 100-120 Auto 0.625-1.25mm 0.8-1.0
Low-dose chest 100-120 Reduced 1.25mm 1.0-1.5

6.4.3 Pediatric Considerations

  • Reduce kVp and mAs based on weight/age
  • Use pediatric-specific protocols
  • Apply "Image Gently" principles
  • Minimize number of phases

6.5 Contrast Administration

6.5.1 Contrast Selection

Indication Contrast Type Concentration
Routine enhanced Low-osmolar 300-350 mgI/mL
CT Angiography Low-osmolar 350-370 mgI/mL
High-risk patients Iso-osmolar 270-320 mgI/mL

6.5.2 Contrast Volume and Rate

Exam Type Volume Rate
Head with contrast 100 mL 1-2 mL/sec
Chest with contrast 100-125 mL 2-3 mL/sec
Abdomen with contrast 100-150 mL 2-3 mL/sec
CT Angiography 75-125 mL 4-5 mL/sec

6.5.3 Timing Methods

  • Fixed delay (empiric)
  • Bolus tracking (threshold trigger)
  • Test bolus (timing determination)

6.6 Image Acquisition

  1. Scout/Topogram

    • Acquire scout images
    • Verify positioning and coverage
    • Set scan range
  2. Pre-Contrast (if applicable)

    • Acquire non-contrast images
    • Assess for baseline findings
  3. Contrast Injection (if applicable)

    • Verify IV patency
    • Program injector parameters
    • Monitor injection
  4. Post-Contrast Acquisition

    • Acquire at appropriate phase(s)
    • Arterial: 25-35 seconds
    • Portal venous: 60-70 seconds
    • Delayed: 3-5 minutes (as needed)
  5. Image Review

    • Review images for quality
    • Assess for artifacts
    • Repeat if technically inadequate

6.7 Post-Examination

6.7.1 Patient Care After Contrast

  • Monitor for 15-30 minutes
  • Assess IV site
  • Provide hydration instructions
  • Advise on potential delayed reactions
  • Metformin patients: follow institutional protocol

6.7.2 Documentation

  • Complete FRM-RAD-001 CT Procedure Log
  • Document dose metrics (CTDIvol, DLP)
  • Record contrast details
  • Note any adverse events
  • Submit images to PACS

6.8 Image Post-Processing

Reconstruction Application
Soft tissue Routine interpretation
Bone Skeletal evaluation
Lung Pulmonary parenchyma
3D/MPR Vascular, complex anatomy
MIP Angiography

7. Contrast Reaction Management

7.1 Reaction Classification

Severity Symptoms Action
Mild Nausea, urticaria (limited), warmth Observe, treat symptoms
Moderate Extensive urticaria, bronchospasm, hypotension Medical treatment, monitor
Severe Anaphylaxis, cardiac arrest, seizure Emergency response, call code

7.2 Emergency Equipment

Available in CT suite:

  • Oxygen and suction
  • Emergency medications (epinephrine, diphenhydramine, etc.)
  • IV fluids
  • Defibrillator/AED
  • Crash cart

8. Radiation Safety

8.1 Dose Monitoring

  • Record CTDIvol and DLP for each exam
  • Compare to diagnostic reference levels
  • Investigate outliers

8.2 Diagnostic Reference Levels

Exam CTDIvol (mGy) DLP (mGy·cm)
Head 60 1000
Chest 15 400
Abdomen 20 700
Abdomen/Pelvis 20 900

9. Quality Control

Activity Frequency
Daily warm-up and calibration Daily
Water phantom QC Daily/Weekly
CT number accuracy Weekly
Spatial resolution Monthly
Physicist review Annually

10. Documentation

  • FRM-RAD-001 CT Procedure Log
  • FRM-RAD-002 Contrast Administration Record
  • FRM-RAD-003 Adverse Reaction Report
  • Dose reports
  • QC logs

11. References

  • ACR Practice Parameter for CT
  • ACR Manual on Contrast Media
  • Image Gently Campaign
  • AAPM CT Protocols
  • State radiation regulations

Revision History

Rev Date Description Author
1.0 [DATE] Initial release [AUTHOR]