Abstract
Objectives:Clinical tumor imaging with 18F-FDG in PET is growing in demand. This article will provide a review of current patient preparation and imaging techniques. The goal is to make the PET study as noninvasive as possible for the patient while obtaining quality images. Communication and coordination when scheduling these studies involves the patient and radiopharmacy, scanner, and support staff. A pertinent patient history (information about weight, pregnancy, breastfeeding, diabetes, etc.) is vital for appropriate patient instructions and patient sequencing. Patient preparation involves many variations on fluid intake, diet, medications, and other factors. Blood glucose levels must be ≤150 mg/dL. If the patient has diabetes mellitus or is glucose intolerant, diet-exercise regime and glucose levels should be monitored. Accurate 18F-FDG dose calculation to be used for region-of-interest analysis or standard uptake value determination is imperative. After 18F-FDG injection, the patient must remain quiet and still to minimize muscle use. Before the scan, the patient may need relaxation medications, urinary catheterization, or other interventions. At the conclusion of this article, the reader should be able to list pertinent patient history issues that are useful for scheduling an 18F-FDG tumor scan, discuss methods to ensure accurate 18F-FDG patient dose calculations, and describe possible methods to help minimize urinary 18F-FDG excretion.
Reimbursed 18F-FDG PET indications are expanding in oncology. The demand for PET as a clinical management tool is escalating. Techniques for performing PET scans are varied. Techniques will continue to change as the new imaging modality increases the scope of practice. The advent of PET and CT scanner integration will enhance the modality. The goal is to make 18F-FDG PET oncologic tumor imaging as comfortable and noninvasive as possible for the patient. This goal is to be accomplished while obtaining accurate, high-quality images.
PATIENT SCHEDULING
Communication and coordination when scheduling these studies is imperative. This involves the patient and staff from the referring physician’s office, radiopharmacy, and scanner unit, as well as ancillary support staff. Obtaining a pertinent patient history allows the PET staff to issue appropriate patient instructions and plan patient sequencing to maintain a flexible facility schedule. Patient information, including a history of diabetes; possibility of pregnancy or breastfeeding; body weight; ability to tolerate the procedure; and need for relaxants, conscious sedation, or general anesthesia, is also critical. Patient information should include results of current anatomic imaging studies, and films should be available at the time of the 18F-FDG study. Information about prior biopsies and surgical interventions is useful. Radiation therapy, chemotherapy, and other medical therapy information is vital and should include dates, doses, and site of therapy.
Diabetic or glucose-intolerant patients need monitoring before the day of the PET study. This monitoring will ensure that the glucose level is ≤150 mg/dL (1). This may require daily monitoring for a few days along with instructions to watch diet and follow exercise recommendations. Diabetic patients may continue to adhere to their oral agents or insulin routines. These medications should not be administered near the 18F-FDG injection time. Insulin administration within 2 h of the 18F-FDG injection time may cause increased glucose uptake in muscle or other soft tissue and compromise tumor uptake (1). If the blood glucose levels are high and cannot be lowered on the day of the study, a patient may have to be rescheduled. In some cases, a diabetic-control specialist may be consulted.
In women of childbearing age, an inquiry regarding the possibility of pregnancy is necessary. It is important for the PET facility and radiation safety personnel to convey the radiation risks to pregnant women and their physicians. The decision to obtain an 18F-FDG tumor scan during pregnancy is a medical decision to be made by the woman and her physician. They must determine whether the benefits outweigh the risks. Management of breastfeeding women usually involves the PET facility radiation safety officer. It is currently recommended that breastfeeding be discontinued for approximately 24 h after the 18F-FDG injection because of 18F-FDG accumulation in breast milk. The normal lactation schedule can be maintained with a breast pump during the 24-h period. A torso tumor scan demonstrates 18F-FDG distribution during lactation in Figure 1. Another method to determine the 18F-FDG accumulation during lactation is to express breast milk and count it in a γ-counter.
Each PET imaging table has a maximum weight-bearing load limit. Some patients may exceed these limits and should not be scheduled for imaging. In some cases, the patient may need to be measured before the scan day or at least before the 18F-FDG injection to ensure their ability to enter the scanner bore comfortably. Idiosyncracies of body size and weight distribution may limit the area of possible imaging even when the table weight-bearing limit is not exceeded. It is vital to make the effort to check these parameters before the 18F-FDG injection to ensure that the area of interest can be imaged optimally.
The ability to tolerate the imaging study is important. Claustrophobic, anxious, or pediatric patients may need special attention. They may require relaxants, conscious sedation, or general anesthesia. This should be scheduled before the day of the PET procedure to arrange family, nursing, and anesthesia support, as well as scanner time and availability. Not all of these situations can be anticipated. Patients in pain also may need to monitor and control their pain by medication or other means (positioning methods, meditation).
The patient history also will help determine whether the patient needs special consideration for the abdomen and pelvis regions. In some cases it may be necessary to enhance the urinary excretion of 18F-FDG during the uptake period and scan. These cases will demand additional effort and time from the patient, PET staff, and ancillary support staff.
Once detailed patient information and history are obtained, the patient may be scheduled. It is important to know at the time of scheduling whether the PET tumor scan will include the brain, torso (orbit through pelvis), or lower extremities. Knowing the indication for the PET scan and the patient’s history of disease is essential in determining the length of the study, informing the patient of the scan’s duration, and scheduling scanner time availability. Most patients with body tumors are imaged from the orbits through the pelvis (30–60 min). A total-body scan, including the brain, torso, and lower extremities (30–90 min), may be indicated on some occasions. PET tumor scans for brain malignancy include only the brain (15–30 min). The additional effort when scheduling a patient is useful in preparing the patient, family, and ancillary support staff and in maintaining the facility schedule and good customer relations.
PATIENT PREPARATION
Patient preparation for 18F-FDG oncologic tumor imaging varies with the patient’s history and abilities. Water intake recommendations vary. The recommendation of 1,418 mL (48 oz) the day before the scan, 709 mL (24 oz) or more the day of the scan, and continued intake after the scan is typical and appropriate. Hydration and frequent bladder voiding decrease the bladder (critical organ) radiation absorbed dose (2). Muscle uptake occurs in nondiabetic patients who are receiving dextrose or lactose in their running intravenous lines. Hyperinsulinemia occurring with carbohydrate administration is likely the cause. This problem can be avoided by the discontinuation of these fluids. The administration of other appropriate fluids should begin 2–4 h before the 18F-FDG injection. These nonglucose fluids may be continued during the scan.
The avoidance of strenuous exercise on the day of the study to limit muscle uptake (muscles use glucose to replace glycogen stores) is recommended (3). In some cases, a patient who is constantly coughing (Fig. 2), chewing, or fidgeting will have increased muscle uptake. Muscle stress, tension, and movement during the uptake portion should be minimized to decrease muscle uptake (Fig. 3). Restful positioning and a calm environment will help reduce stress-related muscle tension. In some situations, the use of a muscle relaxant, such as diazepam, is necessary (1,3,4). This should be given at an appropriate time before the 18F-FDG injection to alleviate muscle uptake. These medications also help anxious or claustrophobic patients tolerate the procedure. It is necessary to make arrangements for a nurse or physician to administer these medications and for a family member to transport the patient home.
Dietary recommendations vary widely from facility to facility. Many of the recommendations have not been well explained but are the result of practice experience. The patient should abstain from caffeine and nicotine for several hours. The effects of caffeine and nicotine on tumor response to glucose have not been documented, but the absence of these drugs may reduce cardiac stimulation and myocardial glucose uptake. The patient may have nothing by mouth (NPO) for 12 h or may have a light breakfast with no sugar the morning of the study and be NPO for 4 h before the study (4). Most medications may be taken with water during the NPO period.
18F-FDG is removed from the human body by excretion in the urinary system. Diuretics and urinary catheterization are used for all patients at some facilities. Other facilities use these methods only when there is a suitable clinical indication. A patient with abdominal or pelvic areas of interest may need to have urinary catheterization and possibly a 3-way continuous flushing catheter to allow clear visualization of structures near or in the bladder or urinary drainage pathways. Diuretics to enhance the excretion of 18F-FDG during the uptake and scan (3,4,6) may be used. When a urinary catheter is used, there should be continual assessment after insertion and throughout the scan. If the catheter is not draining, the bladder will continue to fill with radioactive urine and become uncomfortable for the patient. Special consideration to alleviate radioactive contamination from urine is a must. If urinary contamination occurs, it can cause artifacts and difficulty in scan interpretation. If patients use urinary underpads (Fig. 4), it is advisable to change these just before the 18F-FDG imaging to avoid contamination caused by artifacts. Care must be taken to meet a facility’s radiation safety measures for the radioactive urine and urine-contaminated articles in these cases.
Patients who need conscious sedation or general anesthesia require special consideration and scheduling. It is advisable in such cases to try to perform the 18F-FDG injection before the medication, if possible, to avoid any drug-related changes in 18F-FDG distribution from metabolic or blood flow alterations. Conscious sedation or general anesthesia medication parameters and times should be documented for the interpreting and referring physicians. These parameters should be considered when interpreting the scan.
PATIENT 18F-FDG INJECTION
The patient should be positioned on a bed or in a reclining chair for the injection. The bed or chair can be adjusted so that the patient and technologist are comfortable during the injection and then readjusted to make the patient comfortable during the uptake portion of the study. This will alleviate the need for the patient to walk (which causes muscle uptake) or be moved after the injection. It is imperative for the technologist to spend adequate time before the 18F-FDG injection communicating with the patient about the procedure time sequencing and expectations. Currently, intravenous access is recommended. The intravenous access site should be determined from the patient history and chosen so as to avoid lymph node uptake or dose infiltration in areas of disease (1,3). Intravenous access also assures the technologist that the vein is and will remain viable and provides a method to flush the 18F-FDG dose syringe and intravenous line with saline. Some facilities assume that if the patient is not diabetic that the glucose level at the time of the 18F-FDG injection will be normal. Other facilities monitor the glucose level at the time of the 18F-FDG injection with a glucometer or by serum glucose. The glucometer blood sample can be taken from the intravenous line to be used for the 18F-FDG injection. This eliminates an additional needle stick for the patient. The glucose taken by this method ensures that the glucose level is ≤150 mg/dL. Stress, anxiety, or medications may cause the serum glucose level to be elevated.
The patient should be quiet and lie still in a dimly lit room before the glucose determination and 18F-FDG injection. The technologist should be efficient and timely in the glucose determination, 18F-FDG injection, 20- to 30-mL saline flush, and postinjection activities. A 20- to 30-mL saline flush is useful in reducing the venous retention of 18F-FDG. This should be accomplished with minimal interruption. The patient should be monitored during the uptake period. During the 18F-FDG tumor uptake time the patient should remain quiet and still. The technologist should leave the patient-uptake area at this time and should record dose injection information. The injection site location should be noted in writing to alleviate any concerns when physicians interpret the study. A note should be made of any suspicion of dose infiltration. Dose infiltration will negate the study quantification by region-of-interest (ROI) analysis or standard uptake value (SUV) (3). To ensure accurate ROI and SUV analysis, it is important to assay before and after the 18F-FDG injection syringe with accurate times (5). At some sites, the clocks in the radiopharmacy, patient dosing area, and imaging areas are set to match the PET scanner computer clock or other clock system to maintain accuracy in all the areas. This 18F-FDG dose information may also be entered on the scanner for the patient information and the 18F-FDG tumor imaging study decay corrected for the patient dose data. 18F-FDG injection in central lines or intravenous lines should be performed in cases in which the line and connectors are not in the field of interest. These lines must be flushed with saline to minimize 18F-FDG adherence that may obscure visualization or create artifacts. Documenting the 18F-FDG tumor uptake period is critical for the image decay correction and SUV uptake calculation (5). During the 18F-FDG uptake period, a patient scheduled for an 18F-FDG brain scan should not be allowed any neurologic stimulation. He or she should remain quiet and still in a dimly lit room (1). Brain uptake of 18F-FDG is more rapid than tumor uptake. The 18F-FDG uptake for the brain is approximately 30–45 min. A patient who is to have brain imaging included may be imaged during this period. The 18F-FDG tumor uptake time varies from 60 to 120 min. Patients for whole-body scan (without brain) may be started during this time period.
PATIENT POSITIONING
Patients are requested to empty their bladders or colostomy bags, change diapers or underpads, empty pockets (keys, wallets, etc.), and remove injection site gauze or bandages before positioning on the scanner for the 18F-FDG tumor scan. Artifacts may be caused by an unemptied bladder or colostomy bag with 18F-FDG excretion. Wallets and other items in pockets can create discomfort during the scan. If the clinical indication for the scan includes the neck or esophagus, the patient is asked to take a swallow of water or rinse his or her mouth before the scan to minimize the salivary excretions. The 18F-FDG tumor scan involves patient positioning for patient comfort and anatomic correctness. Special care in positioning is crucial for symmetry of body areas on the transaxial and reformatted images. Extra effort in positioning is important.
It may be helpful to have the patient positioned with his or her head out of the scanner for most of the 18F-FDG tumor scan, if possible. This may help with claustrophobic or anxious patients. Patient positioning must allow for body movement freely through the scanner bore. Extreme care must be taken to place intravenous lines, catheter lines, and all connecting bags, oxygen tubing, safety straps, sheets, and other equipment (e.g., blood pressure cuff, pulse oximeter) in alignment to allow safe movement through the scanner bore for the entire scan time. Patient motion during 18F-FDG tumor imaging creates artifacts or questions about patient position. Technologists must meet this challenge with innovative methods and the use of pillows, cushions, and other props (sandbags, foam, etc.) to decrease motion as a result of discomfort.
The imaging protocol for a clinical indication that involves the head, neck, or upper chest regions should have the imaging begin at the head and continue to the pelvis. Along with the water the patient sipped before positioning, this technique should minimize any 18F-FDG salivary excretions. For clinical indications that involve the pelvis and lower abdomen, the imaging should begin at the pelvis and continue to the head. This will help reduce the bladder artifact and enhance pelvis/abdomen imaging.
Urinary catheter clamping after saline infusion (200 mL) into the bladder before the pelvic images accentuates bladder definition without creating artifacts from intense activity and can be used for appropriate indications. This method can help to visualize abnormal 18F-FDG uptake behind and around the urinary bladder (Fig. 5). After the pelvis imaging is complete (usually in the first 2–3 bed positions), fluid is discontinued and the urinary catheter is unclamped.
Music, books on tape, or CDs may be played or the patient may meditate after any 18F-FDG brain imaging is complete, so that he or she is comfortable and relaxed during the 18F-FDG tumor scan. Some sites use aromatherapy to help patients relax. It is important to note patients’ metal bone pins, pacemakers, etc., so that the physicians will be aware of these items when reviewing transmission and nonattenuated 18F-FDG tumor scans. After the study, the patient should be told to continue with fluid intake to minimize radiation exposure.
CONCLUSION
18F-FDG oncologic tumor imaging is an evolving modality. The advent of CT and PET scanner integration is just one of the advances. Patient, family, referring physician, scheduling secretaries, and ancillary staff education and communication are vital. It is important for technologists and physicians to improve techniques, decrease imaging times, and increase patient comfort while providing quality noninvasive 18F-FDG PET scans. This article is intended to help nuclear medicine technologists and physicians understand some of the challenges involved.
Acknowledgments
The authors wish to thank Rose Busta and Jennifer Johnson for their secretarial support and efforts in completing this manuscript.
Footnotes
For correspondence or reprints contact: Sharon M. Hamblen, CNMT, Division of Nuclear Medicine, Mayo Clinic, 200 First St. SW, Rochester, MN 55905.
E-mail: hamblen.sharon{at}mayo.edu
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