Technetium Sulfur Colloid :Technetium Sulfur Colloid Natasha Dehombre
Objectives :Objectives List all 11 TC Sulfur Colloid procedures
Discuss the Indications as well as the contraindications
Explain Patient prep and doses
Discuss methods of administration /localization for each procedure
Review the acquisitions for each procedure
Explain what is normal and abnormal
Discuss sources of error
ProceduresTechnetium Sulfur Colloid can be used for 11 procedures :ProceduresTechnetium Sulfur Colloid can be used for 11 procedures Bone Marrow Study
Cystography
Esophageal Transit Time
Gastric Emptying Scan
Gastroesophageal Reflux assesment
Gastrointestinal bleed scan LeVeen Denver Shunt
Liver/Spleen Scan
Lymphoscintigraphy
Serosal intercavity infusion
Synovectomy
Bone Marrow Study :Bone Marrow Study Technetium Sulfur Colloid localizes by:
phagocytosis by the reticular cells of the liver, Spleen, bone marrow, and lungs.
The adult dose ranges from: 12 - 15 mCi
Technetium Sulfur Colloid is administered IV, straight stick, or Intravenous catheter flush.
Some indication for the study include:
Evaluation of functional capacity of bone marrow
Evaluation of bone marrow space enlargement
Assessment of bone marrow for metastasis
Bone Marrow Study :Bone Marrow Study There are no Contraindications for this study.
When is comes to patient preparation it is important to:
Identify the patient - Explain the procedure
Void before imaging - Verify Dr’s order
As for acquisitions we will set up:
Statics-100,000 to 200,000 counts
Whole Body- 10-12cm per minute
Bone Marrow StudyThe Difference between normal and abnormal studies are: :Bone Marrow StudyThe Difference between normal and abnormal studies are: In normal studies:
majority of radiotracer will visualize in the axial skeleton
Relative radiotracer uptake is roughly 82% liver, 10% spleen, 8% bone marrow
Active physiologic bone marrow in sternum, vertebral column, shoulders, humerus, pelvis, and femoral heads. In abnormal studies:
Enlarged bone marrow space will present activity through the rest of the bony skeleton
Increased liver and spleen size
Increased visualization outside normal regions may indicate extramedullary hematopoiesis
Bone Marrow Study :Bone Marrow Study During this procedure there can be sources of error or artifacts here is a description of some of the causes.
Liver/spleen uptake will make visualization of lower rib cage, lower thoracic and perhaps upper lumbar vertebrae difficult to analyze
Patients with suppressed RES will affect he diagnostic value of the test.
Lung uptake may indicate colloid clumping with radiopharmaceutical due to aluminum contamination of antacids or androgen therapy
Chemotherapy may cause irregular distribution, hepatomegaly, and /or greater than normal shift to spleen and bone marrow.
Bone Marrow Study :Bone Marrow Study During patient interview patients should answer the following questions
Is there a History or family history of cancer?
If so what type, how long?
Do you have any known blood disorders?
Do you have a history of Liver/Spleen disease?
History of Malaria or tropical disease?
Anemia of any kind?
Any recent trauma
Diabetic?
Feeling lethargic?
High or low blood pressure
Previous MRI, CT, PET scans or Xrays?
Surgery on the bones?
Recent blood work results
Females: pregnant? Nursing?
Toxicity to hematopoietically active bone marrow is a primary limitation of radionuclide therapy. Accurate patient-specific skeletal dosimetry is crucial to avoiding marrow toxicity and tumor underdosing. In current assessments of skeletal dose, deposition of particle energy is tracked within an infinite extent of trabecular spongiosa, with no allowance for particle escape to cortical bone. Paired-image radiation transport (shown here in a model constructed for the right proximal femur) provides a more realistic 3-dimensional geometry for particle transport at both macroscopic and microscopic levels of the skeletal site. :Toxicity to hematopoietically active bone marrow is a primary limitation of radionuclide therapy. Accurate patient-specific skeletal dosimetry is crucial to avoiding marrow toxicity and tumor underdosing. In current assessments of skeletal dose, deposition of particle energy is tracked within an infinite extent of trabecular spongiosa, with no allowance for particle escape to cortical bone. Paired-image radiation transport (shown here in a model constructed for the right proximal femur) provides a more realistic 3-dimensional geometry for particle transport at both macroscopic and microscopic levels of the skeletal site.
Cystography :Cystography Technetium Sulfur Colloid localizes in two ways, Direct (retrograde) and indirect (antegrade)
Direct localization (retrograde): -Compartmental, flows with saline and urine
Indirect localization (antegrade):
-Compartmental, blood (bound to protein and some red blood cells
Cystography :Cystography Adult Dose Range includes:
Direct- .5-1 mCi Indirect- 3-10mCi
Children’s dose range is adjusted to weight
Technetium Sulfur Colloid is administered Direct(retrograde) by injection into foley catheter or Indirect (antegrade) by intravenous injection, butterfly or IV catheter.
Some indications for the study includes:
Evaluation/detection of vesicoureteral reflux
Quantification of post void bladder residual
Evaluation of management and continuing assessment of patients with reflux
Cystography :Cystography The only contraindication for this study is that indirect method is not recommended in patients with known significant renal dysfunction.
When dealing with patient Prep it is important to:
Identify patient -verify Dr’s order
Explain procedure -signed consent
PT must void before -catheterize pt for exam direct cystography
Cystography :Cystography As for Acquisitions, we will set up
Direct flow:
1or2 sec. frames for 30 seconds to 1 minute during filling and voiding segments.
Statics:
120 second images, bladder at full capacity and post void.
Indirect flow and static:
images during void and post void.
CystographyThe Difference between normal and abnormal studies are: :CystographyThe Difference between normal and abnormal studies are: In normal studies:
No visualization of reflux of solution and tracer past bladder during filling and/or voiding.
(normal valve action at ureterovesical junction depends on oblique entry of ureter into bladder, active ureter paraistalisis )
All or nearly all solution is voided from bladder In abnormal studies:
Significant activity in upper urinary tracts during filling, at full capacity and/or while voiding
Reflux is associated with causing UTI’s especially in pediatric patients
Bacterial infections of the kidneys can present with fever, leukocytosis, and bacteremia.
Cystography :Cystography During this procedure there can be sources of error or artifacts here is a description of some of the causes.
Recent contrast radiographic studies may interfer with results.
Contamination of area by infusion leakage, etc
Indirect method: reflux may be missed during filling phase, which is not imaged.
Kidneys may retain radiotracer. Patient may not be able to hold contents of bladder for two hours until imaging or void on command
Cystography :Cystography During patient interview patients should answer the following questions
Do you have a history or family history of renal obstruction or disease?
History or family history of cancer?
History of ureter, bladder, or urethra infections or obstructions?
Any pains or problems with micturition?
Adult female: Pregnant? Nursing?
Intravenous (indirect) radionuclide cystogram Retrograde (direct) radionuclide shows bilateral bladder to ureter reflux. cystogram shows bladder to left ureter At the time of urination (curve 1 reflux. registered above bladder) activity grow above both ureters and kidneys (other curves). :Intravenous (indirect) radionuclide cystogram Retrograde (direct) radionuclide shows bilateral bladder to ureter reflux. cystogram shows bladder to left ureter At the time of urination (curve 1 reflux. registered above bladder) activity grow above both ureters and kidneys (other curves).
Esophageal Transit Time :Esophageal Transit Time Technetium Sulfur Colloid localization is compartmental; esophagus to stomach
The Patient dose ranges from
150-300 microcuries
The methods of administration for this study include:
Po in 15 ml of water, one bolus swallow
Alternative: PO using 1.35 mCi TC99m SC in 50ml of apple sauce
Esophageal Transit Time :Esophageal Transit Time Some indications for this study includes:
Evaluation of esophageal sphincter dysfunction
Evaluation of dysphagia and decreased esophageal motility attributed to achalasia (delay in peristalsis and marked esophageal retention)
Evaluation of PT’s who cannot tolerate manometry or with equivical or negative manometry results having reasonable suggestion of disease.
Evaluation of clinical management by monitoring for serial changes or response to therapy
Evaluation of swallow functioning due to abnormal results on related studies.
Esophageal Transit Time :Esophageal Transit Time Esophageal transit time has no contraindications.
When is comes to patient preparation it is important to:
Identify the PT
Verify Dr’s order
Explain procedure
Ensure PT fasted for 8hrs or over night
Instruct PT as to cooperation with swallowing
As for acquisitions we will set up:
Flow- .23 seconds/15 seconds for 1 minute
Dynamic- 15sec/frame for 9 minutes
Esophageal Transit TimeThe Difference between normal and abnormal studies are: :Esophageal Transit TimeThe Difference between normal and abnormal studies are: In normal studies:
Low count rates or none detectable 5-10 seconds after first swallow
Transit rates >90% after 1 to 8 swallows
<4% of the maximal activity in esophagus by 10 minutes. In abnormal studies:
Transit Rates 5-40% after 8 swallows
In patients with achalasia or scleroderma, transit may be reduced to 20-40%
Diffuse esophageal spasm has significantly reduced transit Rate for first half of study, then normal after 20 swallows
Esophageal Transit Time :Esophageal Transit Time During this procedure there can be sources of error or artifacts here is a description of some of the causes.
Inability to swallow or aspiration of dose
Regurgitation with or without aspiration
Attenuating articles or clothing
Esophageal Transit Time :Esophageal Transit Time During patient interview patients should answer the following questions:
Do you have a history or family history of cancer?
If so what type and how long?
History or esophageal motility dysfunction?
Had any therapy
Trouble swallowing?
Pain when swallowing?
Feel that you must swallow many times to get food down?
Have any abdominal pain?
History of Raynaud’s phenomenon?
History of systemic sclerosis?
History of reflux esophagitis?
Recent or planned esophageal manometry study?
Recent Barium x-ray study?
Females: Pregnant? Nursing?
Gastric Emptying :Gastric Emptying The Localization of Technetium Sulfur Colloid for this procedure is compartmental; moved along with food through gastrointestinal tract
The adult dose for this study is:
100uCi- 1 mCi
In this study TC99m SC is administered in two ways, Solid and liquid:
In solid administration:
Radiotracer is usually mixedwith 1 or 2 whole eggs or egg whites (or oatmeal, beef stew, liver, some use sandwich)
In Liquid administration:
Radiotracer mixed into 120cc water or other (orange juice, milk) for liquid and ingested orally
Gastric Emptying :Gastric Emptying Some indications for this study include
Determination of delayed gastric emptying with quantitation of gastric emptying rate
evaluation of mechanical obstruction
Evaluation of anatomic obstruction (pyloric, postsurgical, post-radiotherapy)
Evaluation of suspected tumors or surgery
The contraindications for this study include:
Allergy to eggs; use oatmeal, baby food, sweet potatoes, chicken or beef livers, or beef stew
Hypoglycemic patient
Gastric Emptying :Gastric Emptying When dealing with patient Prep it is important to:
Identify the PT
Verify Dr’s order
Explain the procedure
Ensure diabetics receive orange juice 2 hrs before test if necessary
Ensure PT to be NPO 4-12 hours before examination
Physician to discontinue sedatives 12 hours before examination.
As for acquisition, we will set up:
Statics
Preset for 60-120 seconds or 50,000 counts
Dynamics
Preset for 60sec/image, 60-90 minutes
Gastric EmptyingThe Difference between normal and abnormal studies are: :Gastric EmptyingThe Difference between normal and abnormal studies are: In normal studies:
Liquid (50%) at 10-56 minutes or 80% in 1 hr with an adult mean of 40 minutes.
Solid (50%) movement out of stomach within a lower limit of 32 minutes to an upper limit of 120 minutes with an adult mean
Terminate study before 60 minutes if gastric emptying becomes > or equal to 95%
T1/2 (50%) for infant given breast milk: 25-45 minutes, or formula or bovine milk: 60-90 minutes In abnormal studies:
Very little or no movement in stomach after 60 minutes. Cause of delayed gastric emptying are mechanical obstruction or altered function
Rapid emptying may occur in cases of “dumping syndrome”
Gastric Emptying :Gastric Emptying During this procedure there can be sources of error or artifacts here is a description of some of the causes.
Burnt eggs; nonuniform mixing of radiotracer
Too much or too little food/ water
Inconsistent amount of food will yield inconsistent data. Each patient should receive the same type, same amount
Patient allergies or intolerance to eggs or food
Patient unable to eat or may vomit or aspirate food and dose
Belt buckles or buttons
Gastric Emptying :Gastric Emptying During patient interview patients should answer the following questions:
Do you have a history or family history of cancer?
If so what type? When?
Diabetic?
Abdominal pains? If so where and since when?
Bloated or acid burning after eating?
Nausea and or vomiting?
History of ulcers?
Hiatal hernia?
Gastric surgery?
On any medications? Relgan or Domperidone?
Had previous related tests?
Female: Pregnant? Nursing?
Gastroesophageal Reflux :Gastroesophageal Reflux The Localization of Technetium Sulfur Colloid for this procedure is compartmental, esophagus to gastrointestinal tract
The adult dose range for this study is
300uCi to 2mCi; 1 mCi or more if acidified orange juice is used.
The methods of administration for this study includes:
Oral (PO) in water, orange juice, milk, wet oatmeal, or saline total of 300ml
PO with acidified orange juice (150ml orange juice and 150ml of 0.1 normal HCI) to delay gastric emptying time and propose the PT to reflux
Ingested through a nasogastric tube if Pt has a history of esophageal motility dysfunction or for children
Gastroesophageal Reflux :Gastroesophageal Reflux Some indications for this study include:
Detection and quantitation of gastroesophageal reflux
Evaluation of Pt’s with diaphragmatic hernia
Evaluation of Pt’s with heartburn regurgitation, or bilious vomiting
Evaluation of children with asthma, chronic lung disease, or aspiration pneumonia
There are no contraindications for this study
Gastroesophageal Reflux :Gastroesophageal Reflux When dealing with patient Prep it is important to:
Identify the PT
-Verify Dr’s order
Explain the procedure
Ensure Pt has fasted for 8 hours or overnight
As for acquisition, we will set up:
Statics 30sec/image; some go for 300,000-500,000 counts
Gastroesophageal refluxThe Difference between normal and abnormal studies are: :Gastroesophageal refluxThe Difference between normal and abnormal studies are: In normal studies
or equal to 4-5% refluxed radiotracer
Activity will appear to be refluxing up the esophagus towards the mouth
For pulmonary aspiration, activity in the lungs. Detection of aspitation during esophageal reflux exams is 0-25%
Gastroesophageal Reflux :Gastroesophageal Reflux During this procedure there can be sources of error or artifacts, here is a description of some of the causes.
Inability to swallow or aspiration of dose
Esophageal retention
Regurgitation with or without aspiration
Attenuating articles or clothing
Patient with known esophageal varices
(potentially life-threatening condition involving dilation of distal esophageal blood vessels usually associated with chronic obstruction of venous drainage from esophageal veins into the hepatic portal system caused by cirrhosis of the liver and alcoholism) perhaps not enough for a contraindication, but consideration may be given to this condition
Gastroesophageal Reflux :Gastroesophageal Reflux During patient interview patients should answer the following questions:
Do you have a history or family history of cancer?
If so what type and for how long?
History of esophageal motility disfunction?
Feel burning or pain in upper abdomen or lower chest after eating?
Have liver disease?
Stomach disease or problem?
After a meal, does it taste like gastric juices when you belch (mini-vomit)?
Female: Pregnant? Nursing?
Gastrointestinal Bleed :Gastrointestinal Bleed Technetium Sulfur Colloid localizes by:
Compartmental, tagged to and circulating with blood.
The Adult Dose range for this study is:
10-20mCi
For this procedure the methods of administration are:
Intravenous injections, or drawing, tagging and reinjection of tagged red blood cells
Gastrointestinal Bleed :Gastrointestinal Bleed Some indications for this study include:
Detection and localization of bleeding sites in patients with active or intermittent gastrointestinal bleeding.
Detection and localization of secondary blood loss as in blood pooling in peritoneal cavity or ruptured arterial venous supplies
Detection and localization of actively bleeding sites for patients with portal hypertension and hypertension to abdominal collateral vessels
Some contraindications for this study include:
Patients with contrast studies under way
Medically unstable patient (uncontrolled hypotension)
Gastrointestinal Bleed :Gastrointestinal Bleed When dealing with patient Prep it is important to:
Identify the PT
-Verify Dr’s order
Explain the procedure
Obtain signed consent for blood work
Instruct Pt to empty bowel and bladder before beginning procedure
If possible have Pt’s or attending nurse look for active signs of bleeding
Check Pt’s current vital signs (blood pressure and heart rate) and assess for orthostatic hypotension
Obtain lab work and information concerning recent blood transfusion
Gastrointestinal Bleed :Gastrointestinal Bleed As for acquisition, we will set up:
Flow:
2-5sec/frame, 60-180 seconds
Dynamics:
60sec/frame for 60 minutes
Statics:
500,000 counts- 2 million counts
Gastrointestinal BleedThe Difference between normal and abnormal studies are: :Gastrointestinal BleedThe Difference between normal and abnormal studies are: In normal studies:
Heart vascular space of liver and spleen and great vessels prominent
Soft tissue uptake Is light and homogeneous
Bladder, bowel, and penile activity not unlikely In abnormal studies:
Flow-focal area of increased activity may also be present
Dynamic study-focal area that may or may not move with time.
Statics-focal area peristalses with time. Blood pool may persist in anbdominal cavity and may or may not move
If little or no movement it may be vascular activity or pool in abdominal cavity. Typical focal areas of active bleeding include ascending, transverse, descending sigmoid colon
Uptake with no change overtime may be inflammatory bowel disease or bad tag excreted into bowel
Gastrointestinal Bleed :Gastrointestinal Bleed During this procedure there can be sources of error or artifacts, here is a description of some of the causes.
Bad radiotracer tag could lead to poor results. Do a thyroid image to confirm bad tag.
Belt buckles articles in clothing, necklaces etc. may attenuate the image
A full bladder may mask the imaging area
Mesenteric varices, uterine or penile blood pool hepatic hemangioma, accessory spleen, and/or renal pelvis of transplanted kidney may may be interpreted as false positives
Intermittence of bleeding compounds the problem of detection
Gastrointestinal Bleed :Gastrointestinal Bleed During patient interview patients should answer the following questions:
Do you have a history or family history of cancer?
If so what type and for how long?
History of bleeding?
Are you bleeding now?
If so for how long? What is the color of the stool?
Do you have active history of internal or external hemorrhoids (non bleeding or actively bleeding)?
Taking aspirin or blood thinners?
Do you have pain?
History of diverticulitis, Crohn’s disease or other diseases?
Colostomy or other surgery?
Ever had endoscopy, CT, upper GI, Barium enema, colonoscopy?
Recent blood transfusions
Recent lab work?
Female: Pregnant? Nursing?
LeVeen Shunt or Denver Shunt Patency :LeVeen Shunt or Denver Shunt Patency Technetium Sulfur Colloid in this study localizes:
compartmentally, peritoneal cavity to blood circulation.
The adult dose range for this procedure:
3mCi
Methods of administration include:
Intraperitoneal injection with local anesthetic by physician
Typically lower left quadrant. Can be guided by ultrasonography to localization of ascites
Usually administered in 7-10 mL of normal saline solution.
LeVeen Shunt or Denver Shunt Patency :LeVeen Shunt or Denver Shunt Patency Some indications for this study include:
Evaluation of LeVeen shunt (peritoneavenous) patency (shunts ascitic fluid from the peritoneal cavity to the venous circulation using a low pressure valve activated by breathing exercises, inserted into the abdominal wall with collection tube inserted through the jugular vein into the superior vena cava
Evaluation of increasing ascites secondary to the use of implanted shunt ex. Increased sodium consumption, inadequate diuretic agents, worsening liver or heart failure
LeVeen Shunt or Denver Shunt Patency :LeVeen Shunt or Denver Shunt Patency The only contraindication for this procedure is:
Patients with pulmonary hypertension may be a consideration with Technetium MAA
When dealing with patient Prep it is important to:
Identify the PT - Verify Dr’s order -Explain procedure
Prepare Pt for intraperitoneal injection
Supplies for procedure:
20-ga needle
25-ga needle
(2) 3 cc syringes
1% lidocaine
3-way stop cock
Sterile gloves
Sterilization solution/ swabs
(3) 4x4 sterile gauzes
Arrange for paracentesis by physician
LeVeen Shunt or Denver Shunt Patency :LeVeen Shunt or Denver Shunt Patency As for acquisition, we will set up:
Flow:
Denver shunt; 3 sec/frame for 60 seconds. Injection directly into pump
Statics:
180-300 sec/image or 500,000 counts
Dynamic:
10 minutes/frame for 6 frames
Whole Body Sweep
Check length of patient, patient orientation, 8-10cm/ minute
LeVeen or Denver Shunt PatencyThe Difference between normal and abnormal studies are: :LeVeen or Denver Shunt PatencyThe Difference between normal and abnormal studies are: In normal studies:
Lung and/or shunt tubing present within 60 minutes. Usually this is a rapid visualization (within 10-30 minutes of injection)
Liver is the target organ within 30 minutes. This method is not presently used as much because of the difficulty of separating the liver from the ascities In abnormal studies:
No activity in the liver after 4 hour delays, indicating obstruction
Activity stops at abdominal pump; very little or no activity in tubing (indicating valve failure or obstruction in tubing.
LeVeen or Denver Shunt Patency :LeVeen or Denver Shunt Patency During this procedure there can be sources of error or artifacts, here is a description of some of the causes.
Risk of infection with injection, Patient should be monitored
Jewelry, medallions, buttons items in shirt pockets, or belt buckles can cause artifacts. Also note any surgically implanted devices.
If little or no visualization of the lungs with visualization of the superior vena cava and right heart, check Pt history for compromising diseases, operations and cancers
If no visualization of radiotracer in abdomen check needle and radiotracer tag
LeVeen or Denver Shunt Patency :LeVeen or Denver Shunt Patency During patient interview patients should answer the following questions:
Do you have a history or family history of cancer?
If so what type and for how long?
Have abdominal pain?
Abdominal distension?
If so more so than before or after surgery?
Female: Pregnant? Nursing?
Intraperitoneal administration of the tracer with scanning time up to 3 hours. Good clearance from peritoneum and tracer uptake in the lungs proves shunt patency. :Intraperitoneal administration of the tracer with scanning time up to 3 hours. Good clearance from peritoneum and tracer uptake in the lungs proves shunt patency.
Liver/Spleen Scan :Liver/Spleen Scan Technetium Sulfur Colloid localizes by:
phagocytosis by the reticular cells of the liver, Spleen, bone marrow, and lungs
The adult dose ranges from: 2-7mCi
The methods of administration for this procedure are:
Intravenous, IV injection or IV catheter and flush. Invert syringe before administering the dose to mix particles
Liver/Spleen Scan :Liver/Spleen Scan Some indications for this study include:
Assessment of anatomy, size and relative position of liver and spleen
Assessment of hepatomegaly, splenomegaly, splenic infarcts, accessory spleen or splenosis
Assessment of benign mesenchymal (kupffer cells) focal lesions (hemangioma, hamartoma) and hepatocellular focal nodular hyperplasia
Assessment of chronic liver or spleen disease
Detection and assessment of hepatic or splenic trauma
Evaluation for liver disease, chronic anemia, leukemia, or other blood disorders.
Evaluation of hepatic infaction
Liver/Spleen Scan :Liver/Spleen Scan The only contraindication for this procedure is:
Study should be performed before any iodinated or barium containing contrast agents. Particularly barium in the colon may result in artificial defects with the liver and spleen.
When is comes to patient preparation it is important to:
Identify the patient
Verify Dr’s order
Explain the procedure
If available write concentrations of alanine amino tranferase, lactate dehydrogenase, and total bilirubin on history sheet
Liver/Spleen Scan :Liver/Spleen Scan As for acquisition, we will set up:
Flow:
1-3 sec/frame for 1 minute followed by immediate static pool (60 seconds or 500,000 counts)
Statics
500,000 – 1 million counts
SPECT
120 stops at 30 sec/stop
Liver/Spleen ScanThe Difference between normal and abnormal studies are: :Liver/Spleen ScanThe Difference between normal and abnormal studies are: In normal studies:
Flow-Because liver is fed 75% by portal system, there should be -6 second delay from aorta presenting to liver presenting. Liver will show dimly at first from aortic flush
Statics-Liver and spleen should have equal heterogeneous distribution with little or no bone marrow uptake
Relative radiotracer uptake is 85% in liver, 10% spleen and 5% bone marrow In abnormal studies:
Colloid shifting presents in marrow, spleen, lungs, and kidneys. These may be caused by severe liver dysfunction
Hotspots: tumors, superior vena cava obstruction, Budd-Chiari syndrome (hepatic thrombosis)
Cold spots: metastatic tumors, hepatomas, adenomas, abscess, cyst, infarction.
Accumulation in renal transplant indicates rejection of that organ
Liver/Spleen Scan :Liver/Spleen Scan During this procedure there can be sources of error or artifacts, here is a description of some of the causes.
Tape marker due to clothes or camera to prevent movement and distortion of holes in marker
For females breast may cause attenuation. Patient can hold them up out of FOV or they can be tapped
Lung uptake caused by aluminum contamination of antacids or virilizing androgen therapy, or large colloid size may indicate colloid clumping within radiopharmaceutical
Increased spleen uptake caused by nitrosources, recent halothane or mrthylcellulose
Decreased spleen uptake caused by chemotherapy, epinephrine, and antimalarials
Deep lesions may be missed
Deep respirations may blur images
Liver/Spleen Scan :Liver/Spleen Scan During patient interview patients should answer the following questions:
Do you have a history or family history of cancer?
If so what type and for how long?
History of liver /spleen disease?
History of tropical diseases?
Abdominal pains?
Recent trauma?
Feeling lethargic?
High blood pressure? Diabetic?
Had any previous related scans X-ray’s or recent barium studies?
Surgery on liver or spleen?
Recent blood work results?
Assess Pt for jaundice and possible alcohol abuse
Hepatic artery catheter?
Had radiation chemotherapy?
Pregnant or nursing?
Taking birth control pills?
Slide 62:99mTc-Sulfur colloid SPECT (fused with simultaneously acquired CT) scan in patient with enhancing liver mass. Colloid uptake in mass typical of focal nodular hyperplasia
Lymphoscintigraphy :Lymphoscintigraphy Technetium Sulfur Colloid localizes by:
Compartmental, phagocytosis
The Adult Dose range for this study:
200uCi- 2 mCi; 450uCi- 1 mCi is typical, two to six injections some up to 7 mCi total.
Methods of administration:
For Melanoma: injections, 2-6 subcutaneous and/or intradermal.
For breast lesions: intraglandular injection 4-6 injections placed into tissue surrounding lesion found by palpitation, needle aspiration or ultrsound.
For lymphedema: Injections, 2 sites per limb, subcutaneous
Lymphoscintigraphy :Lymphoscintigraphy Some indication for the study include:
Evaluation of staging (spreading) of cancers
Evaluation of lymphatic kinetics
Detection of metastatic invasion of the lymph nodes
Evaluation of node resection
Evaluation of chronic lymphedema of swollen extremity
Differentiation of primary and secondary lymphedema
This study does not have any contrindications
Lymphoscintigraphy :Lymphoscintigraphy When is comes to patient preparation it is important to:
Identify the patient
Verify Dr’s order
Explain the procedure
Wipe area with alcohol pad, shave if necessary; clean area with Betadine or chosen sterilizing solution
For breast study patient is to bring mammograms and any related studies with her (outpatient) or make previous related studies available (inpatient)
For breast study Patient is instructed to massage area of injection after injections and between imaging sessions
For lymphedema, physician to instruct patient to wear elastic stockings. These should be removed 3-4 hours before study.
Lymphoscintigraphy :Lymphoscintigraphy As for acquisition, we will set up:
Flow:
30-60 sec/frame, 10-15 minutes
Immediate Statics:
Collect for 5 minutes (300 seconds) every 5 minutes for up to 30 minutes
Whole Body:
Set for 10-15 cm/minute
Delay:
40,000-200,000 counts or 5 minutes each
LymphoscintigraphyThe Difference between normal and abnormal studies are: :LymphoscintigraphyThe Difference between normal and abnormal studies are: In normal studies:
The radiotracer enters the lymphatic systems through normal channels and proceeds through the system into the major lymphatic beds.
Visualizing the sentinel node or nodes is normal within the first Half hour
After 4 hours a chain of activity should visualize in the inguinal, iliac, and/or pre-aortic regions
Liver should also be present
A biopsy of those nodes, once removed will yield the result In abnormal studies:
None or only some of the expected nodes visualizing
Continuity of chain interrupted or abdominal pathway created by tumor replacement of node or lymphatic obstruction
Enlargement of chain width because of lymphoma, congestion, or lymphadenitis
Unexpected intensity difference; reduced in malignant lymphoma or increased in congestion and lymphadenitis
Lymphoscintigraphy :Lymphoscintigraphy During this procedure there can be sources of error or artifacts, here is a description of some of the causes.
A “star” artifact, caused by the intensity of the injection site(s), may obscure nodes in the proximaity from presenting properly
Injection sites that are too distant from the ROI may obscure primary nodes close to the lesion.
the injection (s) may not migrate as expected if there is intervening scar tissue from a prior surgery or injury
One view of the presenting nodes may not be enough to properly locate the nodes or node multiple views including anterior, posterior, oblique, and laterals may be needed
Some nodes are small or weak in intensity. Enough counts and care must be taken to locate all that might be present
Lymphoscintigraphy :Lymphoscintigraphy During patient interview patients should answer the following questions:
Do you have a history or family history of cancer?
If so what type and for how long?
Is this a pre surgery or post surgery study?
Had any surgery in area of interest?
Where is the site/sites under scrutiny?
Had recent biopsies?
Had past or recent related scans PET, CT, MRI etc?
History of lymphedema?
Female: Pregnant? Nursing?
Lymphoscintigraphy after the peritumoral injection. For 1 hr after the injection, dynamic lymphoscintigraphy was performed every 5 min in the anterior and lateral views and then until 2 hr prior to surgery at an interval of 3-6 hr, with static images obtained to monitor the residual radioactivity. :Lymphoscintigraphy after the peritumoral injection. For 1 hr after the injection, dynamic lymphoscintigraphy was performed every 5 min in the anterior and lateral views and then until 2 hr prior to surgery at an interval of 3-6 hr, with static images obtained to monitor the residual radioactivity.
Therapy: Intercavitary (Serosal) :Therapy: Intercavitary (Serosal) Technetium Sulfur Colloid localizes by:
Compartmental to serosal cavity, Macrophages consume colloid particles and become fixed on serosal compartmental lining
The adult dose Ranges from:
2-3mCi
Technetium Sulfur Colloid is administered:
Intracath placement is into cavity of concern through which the therapy is administered
Therapy: Intercavitary (Serosal) :Therapy: Intercavitary (Serosal) Some indication for the study include:
Palliation by reduction of recurrent effusion in serosal cavities secondary to malignant disease, especially those not successfully treated with sclerosing agents such as tetracycling
Prevention of recurrence of malignant disease on serosal surfaces
Treatment of cystic neoplasms
Treatment of malignant ascites(especially ovarian source)
Some contraindications include:
Patients with intraperitoneal infection
Patients with >6monthe life expectancy
Detection of the presence of loculated fluid
Therapy: Intercavitary (Serosal) :Therapy: Intercavitary (Serosal) When is comes to patient preparation it is important to:
Identify the patient
Verify Dr’s order
Explain the procedure
The written directive must be signed by authorized user
Obtain a signed consent from the patient
Patients receiving intrapleural administration must have a thoracentesis to remove the effusion
Therapy: Intercavitary (Serosal) :Therapy: Intercavitary (Serosal) As for acquisition, we will set up:
Statics
250,000 counts or 180 second images
Therapy: Intercavitary (Serosal)The Difference between normal and abnormal studies are: :Therapy: Intercavitary (Serosal)The Difference between normal and abnormal studies are: In normal studies:
Palliation of the pain caused by excess fluid within affected cavity. Maximum effect occurs at 3 month. Dose may need repeating
Temporary therapeutic treatment (remission) of cancer causing the production if excess fluid within the affected cavity
Serosal cavity present as thoroughly and evenly perfused with radiotracer In abnormal studies:
Little no palliative relief of pain and/or cancer causing the production of excess fluid within the affected cavity
Images may have clumping or subspaces with more activity than others
Therapy: Intercavitary (Serosal) :Therapy: Intercavitary (Serosal) During this procedure there can be sources of error or artifacts, here is a description of some of the causes.
Do not use as IV injection, radiotherapy colloid will localize in the liver. The preparation should be a cloudy, brownish green colloidial suspension.
Any leakage from the therapy site must be treated as radioactive spill and cleaned in accordance with precautions pertaining to beta emitters
There are newer non radioisotopic drugs being used for therapy as well as newer Y90 labeled monoclonal antibody and microsphere therapies
Therapy: Intercavitary (Serosal) :Therapy: Intercavitary (Serosal) During patient interview patients should answer the following questions:
Do you have a history or family history of cancer?
If so what type and for how long?
Presently experiencing pain?
If so for how long?
Feel you have fluid build up?
If so how long?
Have results of any other related examinations?
Results of any recent laboratory tests?
Had any other therapy?
If so what type and when?
Female: Pregnant? Nursing?
Therapy: Intra-articular (Joint) Synovectomy :Therapy: Intra-articular (Joint) Synovectomy Technetium Sulfur Colloid localizes by:
Compartmentalization to synovial cavity
The adult dose:
1mCi (weight Based)
Method of administration:
Injection through needle placement into a joint (synovial) cavity.
Some indications include:
Palliation of joint pain caused by rheumatoid arthritis
Palliation of joint pain caused by hemophilic arthropathy
Palliation of joint pain caused by villondular synovitis
Therapy: Intra-articular (Joint) Synovectomy :Therapy: Intra-articular (Joint) Synovectomy For this procedure there are no contraindications
When is comes to patient preparation it is important to:
Identify the patient
Verify Dr’s order
Explain the procedure
The written directive must be signed by authorized user
Obtain a signed consent from the patient
Patients with hemophilia are usually given factor VIII before therapy at 24 and 72 hours after therapy. This is also required In known cases of factor IX deficiency
Patient must bring laboratory results and recent X-ray films of area of interest
Therapy: Intra-articular (Joint) Synovectomy :Therapy: Intra-articular (Joint) Synovectomy As for acquisition, we will set up:
Statics
250,000 counts or 180 second images
Therapy: Intra-articular (Joint) Synovectomy :Therapy: Intra-articular (Joint) Synovectomy In normal studies:
Reduction of pain associated with the affected joint
Reduction of inflammation within the affected joint
Reduction of degradation of cartilage and bone within the affected joint
Improvement of the function of the affected joint
Joint space presents as thoroughly and evenly perfused with radiotracer In abnormal studies:
Little or no palliative effect felt in affected joint
Images may have clumping or subspaces with more activity that others
Therapy: Intra-articular (Joint) Synovectomy :Therapy: Intra-articular (Joint) Synovectomy During this procedure there can be sources of error or artifacts, here is a description of some of the causes.
Extravasation of therapy dose or misplacement of needle will, depending on extent, negatively affect the usefulness of the therapy
Do not use IV injection. Radiotherapy colloid will localize in the liver. The preparation should be a cloudy brownish green colloidal suspension
Therapy: Intra-articular (Joint) Synovectomy :Therapy: Intra-articular (Joint) Synovectomy During patient interview patients should answer the following questions:
Do you have a history or family history of cancer?
If so what type and for how long?
History of joint disease?
Experiencing pain at present?
Results of previous lab tests and/or recent scan results?
What other means of therapy are u currently undergoing?
Recent operations?
Female: Pregnant? Nursing?
Summary :Summary We were able to discuss all 11 Tc99m SC prodecures, Bone Marrow Study Cystography, Esophageal Transit Time, Gastric Emptying Scan, Gastroesophageal Reflux assessment, Gastrointestinal bleed scan, LeVeen Denver Shunt, Liver/Spleen Scan, Lymphoscintigraphy, Serosal intercavity infusion, Synovectomy
Also we were able to discuss the indication as well as the contraindications for all 11 procedures
Took a good look at the precautions that should be taken while performing certain procedures as well as the acquisition for each
We were also able to determine what the essential patient preparations were as well as how to determine what normal and abnormal studies look like
Question1 :Question1 How does Technetium Sulfur Colloid localize in the bone marrow ?
Answer :Answer phagocytosis by the reticular cells of the liver, Spleen, bone marrow, and lungs.
Question 2 :Question 2 What are some indications for a cystograph?
Answer :Answer Some indications for the study includes:
Evaluation/detection of vesicoureteral reflux
Quantification of post void bladder residual
Evaluation of management and continuing assessment of patients with reflux
Question 3 :Question 3 In which procedure is Tc99m SC administered in both solid and liquid?
Answer :Answer Gastric Emptying
Question 4 :Question 4 Where would Tc99m SC localize in a gastroesophageal reflux study
Answer :Answer The Localization of Technetium Sulfur Colloid for this procedure is compartmental, esophagus to gastrointestinal tract
Question 5 :Question 5 What test/scan would be performed given these indications?
Detection and localization of bleeding sites in patients with active or intermittent gastrointestinal bleeding.
Detection and localization of secondary blood loss as in blood pooling in peritoneal cavity or ruptured arterial venous supplies
Detection and localization of actively bleeding sites for patients with portal hypertension and hypertension to abdominal collateral vessels
Answer :Answer Gastrointestinal Bleed
Question 6 :Question 6 What does ETT stand for?
Answer :Answer Esophageal Transit Time
Question 7 :Question 7 What test/scan is
this?
Answer :Answer Liver /spleen scan
Question 8 :Question 8 How does TC99m SC localize in a liver /spleen scan?
Answer :Answer Technetium Sulfur Colloid localizes by:
phagocytosis by the reticular cells of the liver, Spleen, bone marrow, and lungs
Question 9 :Question 9 Name indications for a Lymphoscintigraphy study
Answer :Answer Some indication for the study include:
Evaluation of staging (spreading) of cancers
Evaluation of lymphatic kinetics
Detection of metastatic invasion of the lymph nodes
Evaluation of node resection
Evaluation of chronic lymphedema of swollen extremity
Differentiation of primary and secondary lymphedema
Question 10 :Question 10 These are indications for which type of scan?
Palliation of joint pain caused by rheumatoid arthritis
Palliation of joint pain caused by hemophilic arthropathy
Palliation of joint pain caused by villondular synovitis
A) Therapy: Intercavitary (Serosal)
B) Therapy: Intra-articular (Joint) Synovectomy
C)Palliative therapy
D)Palliative joint therapy
Answer :Answer B) Therapy: Intra-articular (Joint) Synovectomy
References :References Nuclear Medicine Technology: Procedures and quick Reference second edition Pete Shackett 2000 351west camden street BaltimoreMD 21201
Nuclear Medicine and PET/CT sixth edition technologies and techniques edited by Paul E Christian, Kristen M. Waterstram-Rich Rochester Institute of Technology Rochester, New York