Adenocarcinoma of Lung, Lung Cancer, Lung Diseases
Conditions
Brief summary
Patients with suspicious lung lesions were undertaken for PET/CT directed under CT fluoroscopy lung biopsy or robotic-assisted biopsy. The biopsy planning including patient positioning was done after F18-FDG PET/CT whole body or regional imaging of the patient. Written consent was obtained and the patient will be prepared for the biopsy. Lung biopsies were done using a semi-automatic biopsy gun under the imaging guidance (PET fused CT fluoroscopy) following aseptic precautions. Follow-up CT scans were taken post-biopsy. The time consumed for the procedure, radiation exposure to the interventionist, complications and diagnostic yield in both the arms were compared.
Detailed description
Patients with clinical suspicion of lung lesions were recruited for FDG PET/CT. Based on the PET/CT findings and clinical details a PET/CT guided biopsy was planned. The patients were assigned to the two arms. In the first arm, participants underwent a robotic-assisted biopsy. In the second arm, participants underwent PET/CT-directed CT fluoroscopy-guided lung biopsy. The biopsy planning including patient positioning was done after F18-FDG PET/CT whole body or regional imaging of the patient. Written consent was obtained and the patient will be prepared for the biopsy. Lung biopsies were done using a semi-automatic biopsy gun under the imaging guidance (PET fused CT fluoroscopy) following aseptic precautions. Follow-up CT scans were taken post-biopsy. The time consumed for the procedure, radiation exposure to the interventionist, complications and diagnostic yield in both the arms were compared.
Interventions
PROCEDURERobotic arm assisted PET/CT guided biopsy
After preparing the participant for the procedure, the participant was positioned on the PET/CT table with the immobilizer. An automated robotic arm (MAXIO-EX, Perfint healthcare Pvt Ltd, Chennai, India) was used to guide the needle for biopsy. Co-axial 18 G biopsy needle (BARD Biopsy disposable coaxial biopsy needle pack, Bard Peripheral Vascular, Inc., Arizona, USA) was inserted according to the orientation planned by the robotic biopsy device. After the location is ensured, the trocar stylet is removed from the coaxial cannula and specimens were retrieved using a semiautomated biopsy gun. A repeat CT chest was acquired two hours after the procedure to rule out post-procedural complications. Complications during the procedure were noted, and immediate management was done.
PROCEDUREPET fused CT-Fluoroscopy guided biopsy
CT fluoroscopy was used to place the biopsy needle to the FDG avid lung lesion
Sponsors
Post Graduate Institute of Medical Education and Research, Chandigarh
Study design
Observational model
OTHER
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes
Inclusion criteria
1. Age \>/= 18 years 2. FDG avid amenable lung lesion 3. INR \< 1.2 and Platelet counts \> 80,000/mm3
Exclusion criteria
1. Participants with pre-existing bleeding diathesis like hemophilia, coagulopathy defined by INR ≥ 1.2 and Platelet counts ≤ 80,000/mm3 2. Participants who refuse to provide the written informed consent 3. Signs of hypoperfusion like cyanosis, hypotension etc. 4. Presence of hypoxemia (SpO2 \< 95% -measured in a pulse oximeter) 5. Pregnant/Lactating females participants 6. Non-cooperative participants 7. Inaccessible lesions (based on the decision made on pre-biopsy planning) 8. CoVID-19 positive participants
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| To compare the accuracy ( in percentage) of trans-thoracic percutaneous PET fused CT-fluoroscopy guided lung biopsy and automated robotic arm assisted PET/CT guided lung biopsy | three months | Histology reports of the biopsies were recorded and the mutation analysis, Adequacy of the sample was decided by the pathologist who received the sample and when inadequate, we were notified accordingly by the Department of Pathology. The histopathological results were analyzed. True positive, True negative False-positive and False-negative were calculated for both the groups. The diagnostic accuracy in percentage for both arms will be calculated and compared. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| To compare the radiation exposure and complication in the both arms | three months | Procedure related complications and radiation exposure to the participants and interventionist were noted in the both arms. |
Countries
India
Outcome results
None listed