On this page
Asset Type
Manufacturer
Model
What This Guide Helps With
Troubleshoots PET or CT image artifacts and degraded quality caused by positioning, motion, accessories, contamination, protocol selection, calibration, or environmental factors.
Step-by-Step Troubleshooting
1. Protect the Patient From Unnecessary Repeat Imaging
Do not repeat CT exposures or PET acquisitions solely to investigate an unexplained image-quality problem without first checking obvious external causes.
If diagnostic image quality cannot be assured, stop clinical use of the affected acquisition path and move the patient to another verified system when necessary.
Expected outcome: The patient is not subjected to unnecessary repeat imaging and questionable images are not relied upon clinically.
2. Characterize the Image Problem
Determine whether the issue affects:
- CT images
- PET images
- Fused PET / CT images
- One examination or multiple patients
- One protocol or all protocols
- A specific anatomical region
- All reconstructed series
Review when the artifact first appeared and whether it is repeatable.
Expected outcome: The artifact is categorized well enough to guide external troubleshooting.
3. Check Patient Motion and Positioning
Review the study for motion, mispositioning, or inconsistent positioning between acquisitions.
Check whether:
- The patient moved
- Arms or body position changed
- Respiratory motion may have affected alignment
- The patient was uncomfortable or unable to remain still
- Positioning devices shifted
Expected outcome: Patient movement and positioning are either identified as the likely cause or reasonably ruled out.
If positioning or motion explains the issue and a repeat study is clinically authorized, correct the setup before reacquisition.
4. Inspect External Objects and Accessories
Check the scan field and patient setup for objects that can introduce artifacts, including:
- Monitoring leads
- Cables
- Metallic objects
- Positioning aids
- Clothing hardware
- External devices
- Accessories inadvertently left in the imaging field
Also inspect approved scanner accessories for damage or incorrect placement.
Expected outcome: No avoidable external object or damaged accessory is affecting image quality.
5. Confirm Correct Protocol and Reconstruction Selection
Verify that the intended clinical protocol, acquisition mode, reconstruction selection, and operator-accessible image settings were used.
Compare with a known-good examination or approved department configuration when appropriate.
Do not alter service calibration or restricted reconstruction parameters.
Expected outcome: The imaging workflow uses the intended approved configuration.
6. Determine Whether the Problem Is Patient-Specific or System-Wide
Review recent studies or approved test images to determine whether the artifact occurs:
- Only with one patient
- Only with one protocol
- Only with one accessory
- Across multiple unrelated examinations
Avoid using patient exposures solely as a troubleshooting test.
Expected outcome: The issue is narrowed to a patient/workflow cause or a reproducible equipment-related condition.
7. Inspect the Accessible Imaging Area
Inspect accessible surfaces and components around the patient opening and table for:
- Foreign material
- Fluid contamination
- Damaged covers
- Loose accessories
- Objects in the imaging path
- Visible physical damage
Do not open detector or gantry covers.
Expected outcome: Accessible imaging surfaces and the scan path are clean, intact, and unobstructed.
8. Review Calibration and Quality-Control Status
Determine whether required calibration or quality-control procedures are current and whether any recent QC test showed abnormal results.
If an approved operator-level or Clinical Engineering QC procedure is appropriate, perform it using designated phantoms and test equipment.
Expected outcome: Quality-control results are acceptable and do not reproduce the image-quality problem.
If QC passes and the external cause has been corrected, proceed to final verification.
9. Verify Image Quality Before Return to Service
Use approved test procedures to verify the affected modality.
Confirm:
- No reproducible unexplained artifact remains
- Images reconstruct normally
- PET / CT registration is appropriate when applicable
- No new fault appears
- Required QC criteria are met
Expected outcome: Image quality is acceptable according to applicable department and manufacturer requirements.
If required image-quality testing passes, troubleshooting can stop and the scanner may be returned to service.
If the Problem Persists
If patient motion, positioning, external objects, accessories, protocol selection, accessible contamination, and approved quality-control checks have been ruled out but artifacts persist, the cause may involve detector performance, calibration, acquisition electronics, reconstruction, motion correction, PET / CT registration, mechanical alignment, or another service-level condition.
The system should be:
- Removed from service when image reliability is uncertain
- Labeled Out of Service
- Sent for repair or formal system evaluation
- Evaluated using appropriate GE Healthcare documentation, phantoms, and approved test equipment
- Calibrated, repaired, or configured only by qualified personnel
Do not compensate for unexplained system artifacts by changing clinical settings without determining the cause.
Following service, complete required image-quality and calibration testing before return to clinical use.
Knowing when to stop external troubleshooting and escalate is proper troubleshooting.
Clinical Use Tip
Compare questionable PET / CT images with positioning, motion, accessories, and recent QC results before repeating a patient scan or assuming detector failure.
Work Order Documentation (CCR Method)
CCR = Complaint, Cause, Resolution
Complaint
What was reported by the clinical staff.
Example:
"Imaging staff reported a repeatable artifact on Discovery MI CT images that was not present on prior studies."
Cause
What was observed during troubleshooting.
Example:
"Clinical Engineering found a removable positioning accessory with metallic material left within the imaging field during the affected examinations."
Resolution
What action was taken.
Example:
"Clinical Engineering removed the accessory, completed approved image-quality verification, confirmed the artifact was no longer present, and returned the scanner to service."
Helpful Details to Include (If Known)
- PET, CT, or fused images affected
- Artifact appearance and location
- Patients or protocols affected
- Patient movement
- Positioning details
- Accessories in the scan field
- Recent configuration changes
- QC status
- Test phantom result
- Final image-quality result
Final Thought
Poor image quality should be investigated systematically before internal failure is assumed. Protect the patient from unnecessary repeat imaging, verify positioning, motion, accessories, protocol selection, and QC status, and escalate when a reproducible artifact remains unexplained.
That is successful troubleshooting.