NMT » Case Studies » Current Case


Imaging Gastro Intestinal
Bleeding in Nuclear Medicine

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Tiffany MaGill, student nuclear medicine technologist,
Medical College of Georgia

Cherry Lim, NMT, Aiken Regional Hospital, Aiken, SC

Mary Anne Owen, M.H.E., RT(N)
Program Director, Nuclear Medicine Technology,
Medical College of Georgia

Deborah Gibbs, B.S., CNMT, RT(N)
Clinical Education Coordinator, Nuclear Medicine Technology
Medical College of Georgia



NMT Technologists' Considerations (click to view)

Organ / Pathology

RPH and Dose

Method of Localization

Method of Administration

Route of Excretion

  Biodistribution

  Pitfalls

 

GI Bleed

Indications: Bright Red or Maroon Blood from the rectum

…recent polypectomy, vascular malformation, low hematocrit or hemoglobin

 

 

Tc99m RBC UltraTag 20-50 mCi –best for intermittent bled

(can also use Tc 99m Sulfur Colloid for acute bleed, 10-20 mCi)

 

 

Compartmentalization to the blood vessels and to areas of GI bleeding.

 

 

IV inj. of pt.’s tagged blood

 

Renal System

 

Spleen (critical), bladder, kidneys, blood, heart, liver

 

Very hot spleen can indicate blood lysis during the tagging process.

Introduction of  air into vial or failure to vent air from vial can cause TcO4 to dissociate quickly demonstrating free tech

 Contamination:  take lateral to differentiate surface activity from bowel

  Collimator

Mode (D or PL)

Counts or Time

  Views

Energy Windows

Patient Prep

Drug Interventions and Findings

 

Low Energy High Res. Par. Hole

 

Flow: D

Pool: D

(Planar Scan type)

 

Flow: 16 frames, 4s ea.

Pool: 12 frames, 5 min. ea.

Delay: 1 frame, 5 min.

 

Size: 128x128

ANT for all views, flow and pool.

 

140 keV, 20% window

 

Collect pt. blood sample (1-3 mL) using Heprin or ACD as anticoagulant.

 

Location of bleeding in the GI tract, esp. in the intestines.

Most positive scans visualize from 60-90 minutes.  Splenic Flecture, illeocecal junture, sigmoid colon, and hepatic flecture common sites for bleeding.

 



Discussion (click to view)
Successful management of GI bleeding patients often depends on accurate localization of the bleeding site. While upper GI tract bleeding sites can be located with endoscopy and selective arteriography in most cases, lower GI bleeds are most often located with Nuclear Medicine GI bleed imaging due to its very high sensitivity. Nuclear medicine studies can detect bleeding rates as low as 0.05 to 0.1mL/min, while angiography will only demonstrate active bleeding at a rate of 0.5mL/min. or greater. If the nuclear medicine study is positive, then angiography can be helpful in further characterizing the bleeding site and sometimes for therapeutic reasons. Tc99m sulfur colloid and Tc99m RBCs are used in GI bleed studies. Sulfur colloid is primarily used for active bleeds, while tagged RBCs are best suited for intermittent bleeds. A primary diagnostic challenge that may foil proper localization of the bleeding site is the tendency of bleeding to be intermittent in nature regardless of the cause. For this reason, delayed images may be necessary in order to localize the bleeding site. Radioactivity that moves over time, is indicative of movement of blood into and through the GI tract, while fixed focal areas typically represent vascular formations. Some false positive findings may include accessory spleen in sulfur colloid scan, kidney and bladder activity in Tc99m RBCs scan, and also in varices or other vascular abnormalities. However, these areas will not demonstrate movement in the bowel lumen in subsequent images, which is necessary in a true positive scan. Cine views can be especially helpful in observing intraluminal transit (Early).



Findings (from radiologist’s reports)


The radiologist noted an area of hyperemia (what is this?) in the right upper quadrant on the flow images. On the pool images, there were several focal areas of activity noted. In frame 17, there is a focal area in the right lower quadrant and right upper quadrant. In frame 18, there is one in the left upper quadrant and right lower quadrant. In frame 19, all three areas show high activity. Frames 20 and 21 don’t definitely demonstrate any focal areas of activity. In frames 22 through 24, there is an area of focal activity in the right upper quadrant, and in the 25th, the left upper quadrant area reappears as well as the right lower quadrant area. In the last 3 frames, there is an area of intense activity in the right upper quadrant with linear configuration suggestive of transverse colon. Delayed images demonstrated focal areas in the right upper and lower quadrants. Overall impression was that this was a positive GI bleed scan. Though the pictures were confusing, they were very suggestive of right colonic focus, which could be cecum or near the hepatic flexure. The radiologist was confident that vasopressin injection should cover both those regions. The patient was immediately taken in for a visceral angiogram to more accurately locate and treat the bleeding. While a pinpoint bleed was not located, an area of hyperemia was found in a short segment of bowel near the hepatic flexure, which corresponded with the location noted on the GI bleed scan pool pictures, and could represent inflammation angiodysplasia (an abnormal growth or formation of blood vessels). An 80% stenosis of the right common femoral artery was also found during the angiogram, which can be seen somewhat on pool pictures as well.


Instructor's Comments:

Q: What is hyperemia?

Patient History


The patient had a recent polypectomy, and it was suspected that the bleeding could be coming from the areas where polyps were removed. The patient was admitted one day prior for rectal bleeding. On the morning of the GI bleed scan, the patients hemoglobin and hematocrit levels were both below the normal range.

Instructor's Comments:

Q: What is considered normal range?



Radiopharmacy


The radiopharmaceutical used for this GI bleed scan was Tc99m UltraTag RBCs. It is ideal for GI bleed imaging because is localizes via compartmentalization to the blood vessels and areas of GI bleeding (Shackett). The tagging process is accomplished when Tc99m pertechnetate diffuses across the RBC membrane and is reduced by intracellular stannous ions that are injected into the reaction vial from the first syringe in the kit. After the Tc99m pertechnetate has been reduced, it cannot diffuse back out of the cell (UltraTag Package Insert).

Instructor's Comments:
Q: What happens if air is not vented from the reaction vial? What tagging deficiency will occur from this occurrence?
Q: How can this phenomenon be demonstrated on the patient scan?


Normal biodistribution includes the spleen (which is the critical organ), bladder, kidneys, blood, heart, and liver. Increased uptake in the spleen can indicate blood lysis during the tagging process, which could be due to handling the blood too roughly while mixing (Debra Gibbs). A positive scan will show increased activity within the intestinal lumen.



Patient Preparation


Patient preparation included first drawing a 1-3mL blood sample for tagging. In this case, the in-patient had an existing IV access, which was used to draw the blood. The blood is then tagged with 20-50mCi of Tc99m Pertechnetate. Directly before the scan, the patient is positioned and then the tagged blood is injected back into the patient, in this case using the existing IV access. This particular patient received a 24.5mCi dose. Flow and pool images are then acquired, and sometimes delay images may be requested by the radiologist.



Instrumentation


The Picker PrismXP Gamma Camera was positioned over the patient’s abdomen as close as possible to optimize image resolution. The Odyssey software protocol for a Tc99m GI Bleed scan was selected. Energy window is 20%, collimators are low energy high resolution parallel hole. Dynamically acquired planar flow images are set at 16 frames at 4 seconds each, and dynamically acquired planar pool images are set at 12 frames at 5 minutes each. If delayed images are needed, the Odyssey protocol for GI Bleed Delays is selected, and views are set at 5 minutes each. Patient position is the same as the flow and pool images.



Positioning


The patient was positioned supine on the table and covered with a blanket since it was very cold in the room. The patient was instructed not to move, but was asleep through most of the scan, so movement wasn’t a problem.



Processing


Images were not adjusted or rescaled for intensity. The images were presented with flows first, then pools, and delays on a separate film. The radiologist reading the pictures also came into the scan room to view the cine view of the flow and pool pictures to get a better idea of where the activity was traveling.


References (click to view)


Early, Paul J., & Sodee, D. Bruce. (1995). Principles and Practice of Nuclear Medicine
(2nd ed.).
St Louis, MO: Mosby, Inc.


Shackett, Pete. (2000). Nuclear Medicine Technology: Principles & Quick Reference. Philadelphia, PA: Lippincott Williams & Wilkins.


October 2001