Archived Policies - Radiology
Positron Emission Tomography (PET)
Positron emission tomography (PET) or positron emission tomography/computed tomography (PET/CT) may be considered medically necessary for treatment strategy planning for known or suspected malignancy (except screening, surveillance) when the following criteria are met:
A. Initial Treatment Strategy Planning
1. PET or PET/CT imaging may be considered medically necessary for initial treatment strategy planning prior to obtaining tissue biopsy confirmation when the findings on other imaging modalities (e.g., computed tomography [CT], magnetic resonance imaging [MRI], or ultrasound [US]) are inconclusive and/or discordant; AND
2. PET or PET/CT imaging may be considered medically necessary for initial treatment strategy planning after tissue biopsy confirmation of the malignancy and prior to performance of any chemotherapy, surgical and/or radiation treatment when the:
B. Subsequent Treatment Strategy Planning
PET or PET/CT imaging for subsequent treatment strategy planning may be considered medically necessary:
*NOTE: “Restaging” should not be confused with routine follow-up or monitoring for possible recurrence. Restaging is done when there is clinical suspicion of recurrent disease and, like initial staging, tests are performed to determine the extent of the recurrence. This often means going through the same process that was done when the cancer was first diagnosed: exams, imaging tests, biopsies, and possibly surgery to restage the cancer.
C. Surveillance and Screening
Cardiac PET scanning may be considered medically necessary as a technique to assess myocardial perfusion defects when the patient has at least intermediate risk for coronary artery disease AND the following criteria are met:
Cardiac PET scanning may be considered medically necessary to assess the myocardial viability in patients with severe left ventricular dysfunction as a technique to determine candidacy for a revascularization procedure.
Positron emission tomography (PET) or positron emission tomography/computed tomography (PET/CT) may be considered medically necessary for the following:
NOTE: Appropriate candidates are those patients who have complex partial seizures that have failed to respond to medical therapy and who have been advised to have a resection of a suspected epileptogenic focus located in a region of the brain accessible to surgery. Conventional techniques for seizure localization must have been tried and provided data that suggested a seizure focus, but were not sufficiently conclusive to permit surgery.
EEG's AND PET EXAMINATION: The purpose of the PET examination should be to avoid subjecting the patient to extended pre-operative electroencephalographic recording with implanted electrodes.
Positron emission tomography (PET) or positron emission tomography/computed tomography (PET/CT) is considered experimental, investigational and unproven for all other indications.
PET scans are based on the use of positron emitting radionuclide tracers coupled to organic molecules, such as glucose, ammonia, or water. The radionuclide tracers simultaneously emit two high-energy photons in opposite directions that can be simultaneously detected (referred to as coincidence detection) by a PET scanner, consisting of multiple stationary detectors that encircle the area of interest.
A variety of tracers are used for PET scanning, including oxygen-15, nitrogen-13, carbon-11, and fluorine-18. Because of their short half-life, tracers must be made locally, the majority requiring an on-site cyclotron.
This policy only addresses the use of radiotracers detected with the use of dedicated PET scanners. There is a similar procedure to PET that may be referred to as FDG-SPECT (fluorodeoxyglucose-single photon emission computed tomography), metabolic SPECT, or PET using a gamma camera. In this procedure radiotracers such as FDG may be detected using SPECT cameras.
Surveillance is closely monitoring a patient's condition, looking for sign(s) that a cancer has returned, but withholding treatment until symptoms appear or change; also called observation, watchful waiting, and expectant management.
The purpose of a cancer screening test is to identify the presence of a specific cancer in an individual who does not demonstrate any symptoms. Examples of cancer screening tests are the mammogram (breast), colonoscopy (colon), Pap smear (cervix), and PSA blood level and digital rectal exam (prostate).
PET/CT Fusion Imaging
PET/CT Fusion Imaging is a new diagnostic tool for the staging and restaging of cancer. Patients can be examined with both PET and CT in a single examination. This new technology correlates two simultaneous imaging modalities for a comprehensive examination that combines anatomic data with functional or metabolic information. The CT images are used for anatomic reference of the tracer uptake patterns images in PET, as well as for attenuation correction of the PET data.
Cardiac Pet Scan
In terms of myocardial perfusion studies, patient selection criteria for PET scans involve an individual assessment of the pretest probability of coronary artery disease (CAD), based on both patient symptoms and risk factors. Patients at low risk for CAD may be adequately evaluated with exercise electrocardiography. Patients at high risk for CAD may not benefit from a non-invasive assessment of myocardial perfusion, since, in this setting, a negative test may represent a false negative result. These patients may be immediately referred to coronary angiography.
Patient selection criteria for PET scans for myocardial viability are typically those patients with severe left ventricular dysfunction who are under consideration for a revascularization procedure. A PET scan may determine whether the left ventricular dysfunction is related to viable or nonviable myocardium. Patients with viable myocardium may benefit from revascularization, while those with non-viable myocardium will not. As an example, PET scans are commonly performed in potential heart transplant candidates to rule out the presence of viable myocardium.
For both perfusion and viability study indications, a variety of studies have suggested that the PET scans are only marginally more sensitive or specific than SPECT scans. Therefore the choice between a PET scan (which may not be available locally) and a SPECT scan represents another clinical issue. PET scans may provide the greatest advantage over SPECT scans in obese patients where tissue attenuation of tracer is of greater concern.
This policy is based on multiple evaluations of PET, including Blue Cross Blue Shield Association (BCBSA) Technology Evaluation Center (TEC) Assessments, other systematic reviews, meta-analyses, decision analyses, and cost-effectiveness analyses. In the TEC Assessments, PET scanning was considered an adjunct to other imaging methods (i.e., CT, MRI, ultrasonography), often used when previous imaging studies are inconclusive or provide discordant results. In this setting, the clinical value of PET scans is the rate of discordance among imaging techniques and the percentage of time that PET scanning results in the correct diagnosis, as confirmed by tissue biopsy.
According to The National Comprehensive Cancer Network (NCCN), the most common use of PET scanning is related to oncology, especially in staging and managing lymphoma, lung cancer, and colorectal cancer; however, PET scan has a role in most other types of cancers. The National Comprehensive Cancer Network 2009 updated Clinical Practice Guidelines in Oncology includes new limited indications for the use of PET scans for ovarian, small cell lung, soft tissue sarcoma, and pancreatic cancers.
In 2003, the American College of Cardiology (ACC) and the American Heart Association (AHA) published updated guidelines for cardiac radionuclide imaging. Cardiac applications of PET scanning were included in these guidelines. The ACC/AHA guidelines categorize specific indications for PET scanning:
The medically necessary indications for PET myocardial perfusion studies in this policy are consistent with Class I and Class IIa indications in the ACC guidelines.
PET has perhaps been most thoroughly researched as a technique to assess myocardial viability to determine candidacy for a coronary revascularization procedure. For example, a patient with a severe stenosis identified by coronary angiography may not benefit from revascularization if the surrounding myocardium is non-viable. A fixed perfusion defect, as imaged on SPECT scanning or stress thallium echocardiography, may suggest non-viable myocardium. However a PET scan may reveal metabolically active myocardium, suggesting areas of hibernating myocardium that would indeed benefit from revascularization. The most common PET technique for this application consists of N-13 ammonia as a perfusion tracer and FDG as a metabolic marker of glucose utilization. A pattern FDG uptake in areas of hypoperfusion (referred to as FDG/blood flow mismatch) suggests viable, but hibernating myocardium. The ultimate clinical validation of this diagnostic test is the percentage of patients who experience improvement in left ventricular dysfunction after revascularization of hibernating myocardium, as identified by PET scanning.
SPECT scanning may also be used to assess myocardial viability. For example, while initial myocardial uptake of thallium-201 reflects myocardial perfusion, redistribution after prolonged periods can be used as a marker of myocardial viability. Initial protocols required redistribution imaging after 24 to 72 hours. While this technique was associated with a strong positive predictive value, there was a low negative predictive value, i.e., 40% of patients without redistribution nevertheless showed clinical improvement after revascularization. The negative predictive value has improved with the practice of thallium reinjection. Twenty-four to 72 hours after initial imaging, patients receive a reinjection of thallium and undergo redistribution imaging.
The ACC/AHA guidelines conclude that PET imaging “appears to have slightly better overall accuracy for predicting recovery of regional function after revascularization in patients with left ventricular (LV) dysfunction than single photon techniques (i.e., SPECT scans).” However, the ACC guidelines indicate that either PET or SPECT scans are Class I indications for predicting improvement in regional and global LV function and natural history after revascularization, and thus do not indicate a clear preference for either PET or SPECT scans in this situation.
Further supporting the equivalency of these two testing modalities, Siebelink and colleagues performed a prospective randomized study comparing management decisions and outcomes based on either PET imaging or SPECT imaging in 103 patients with chronic coronary artery disease and left ventricular dysfunction who were being evaluated for myocardial viability. Management decisions included drug therapy or revascularization with either angioplasty or coronary artery bypass grafting. This study is unique in that the diagnostic performance of the two studies was tied to the actual patient outcomes. No difference in patient management or cardiac event-free survival was demonstrated between management based on the two imaging techniques. The authors concluded that either technique could be used for management of patients considered for revascularization with suspicion of jeopardized myocardium.
In patients with symptoms suggestive of CAD, a central clinical issue is to determine whether a coronary angiogram is necessary for further work-up. A variety of non-invasive imaging tests, including PET (using rubidium-82) and SPECT scans, have been investigated as a means of identifying reversible perfusion defects, which may reflect coronary artery disease, and thus identify patients who may benefit from further work-up with an angiogram. The following table summarizes the ACC guidelines for myocardial reperfusion for both SPECT and PET scans in patients with an intermediate risk of coronary artery disease
Identify extent, severity, and location of ischemia (SPECT protocols vary according to whether patient can exercise).
Repeat test after 3–5 years after revascularization in selected high-risk asymptomatic patients (SPECT protocols vary according to whether patients can exercise).
As initial test in patients who are considered to be at high risk (i.e., patients with diabetes or those with a more than 20% 10-year risk of a coronary disease event) (SPECT protocols vary according to whether patients can exercise).
Myocardial perfusion PET when prior SPECT study has been found to be equivocal for diagnostic or risk stratification purposes.
As noted in the table, the data and consensus opinion (as reflected by a Class I designation) favors limiting a PET scan to those situations in which a prior SPECT scan is inconclusive. In the text summary, the guidelines note, “Overall, because of the higher resolution of PET and the routine application of attenuation correction, it is probable that sensitivity and specificity are slightly higher for PET compared with SPECT, but there is not a robust database of head-to-head comparisons.” The previous 1995 version of the guidelines stated, “PET is an expensive imaging modality, and whether the greater cost of PET is justified by a possible improvement in diagnostic accuracy requires further rigorous study. Thus, until data from large-scale, definitive studies are published, PET is considered an effective modality for the noninvasive diagnosis of coronary artery disease but should be considered for routine diagnostic purposes only if the costs of PET are equivalent to or less than the costs of SPECT imaging in the same community.” This discussion of the relative costs of PET and SPECT has been eliminated in the 2003 version of the guidelines.
Studies continued to show the equivalence of SPECT and PET. As one example, Slart and colleagues concluded that there was overall good agreement between SPECT and PET for the assessment of myocardial viability in patients with severe LV dysfunction. Comparative studies reported on test accuracy and did not address impact on clinical outcomes.
While comparative studies were identified for SPECT compared to PET in the evaluation of CAD, the comparative data are still limited. Using a thorax-cardiac phantom, Knesaurek concluded that PET was better at detecting smaller defects. In this study, a 1 cm (centimeter) insert was not detectable by SPECT, yet it was detectable using PET. Merhige reported on outcomes of non-contemporaneous patients with similar probabilities of CAD who were evaluated by SPECT or PET. In this study involving PET scans done at one center compared to those evaluated by SPECT, those receiving PET evaluations had lower rates of angiography (13% versus 31%) and revascularization (6% versus 11%) with similar rates of death and MI at one year of follow-up. These results were viewed as preliminary and additional comparative studies showing impact on outcomes are needed.
The sensitivity and specificity of PET may be slightly better than SPECT. However, their diagnostic utilities are similar in terms of altering disease risk in a manner affecting subsequent decision making among patients with intermediate pretest probability of CAD. For example, a patient with a 50% pretest probability of CAD would have a 9% post-test probability of CAD following a negative PET scan compared to 13% after a negative SPECT. In either case, further testing would not likely be pursued.
Another consideration is that there are fewer indeterminate results with PET than SPECT. A retrospective study by Bateman et al. matched 112 SPECT and 112 PET studies by gender, body mass index, and presence and extent of CAD, and they were compared for diagnostic accuracy and degree of interpretative certainty (age 65 years; 52% male; mean BMI = 32 kg/m2; 76% with CAD diagnosed on angiography). Eighteen of 112 (16%) SPECT studies were classified as indeterminate compared to 4 of 112 (4%) PET studies. Liver and bowel uptake were believed to affect 6 of 112 (5%) PET studies, compared to 46 of 112 (41%) SPECT studies. In obese patients (BMI > 30), the accuracy of SPECT was 67% versus 85% for PET; accuracy in nonobese patients was reported to be 70% for SPECT and 87% for PET. Therefore, for patients with intermediate pretest probability of coronary artery disease, one should start with SPECT testing and only proceed to SPECT in indeterminate cases. Additionally, since obese patients are more prone to liver and bowel artifact, PET testing is advantageous over SPECT in severely obese patients.
In 2005, a joint statement from the Canadian Cardiovascular Society, Canadian Association of Radiologists, Canadian Association of Nuclear Medicine, Canadian Nuclear Cardiology Society, Canadian Society of Cardiac Magnetic Resonance recommended (Class I recommendation, level B evidence) “PET scanning for patients with intermediate pretest probability of CAD who have nondiagnostic noninvasive imaging tests or where such a test does not agree with clinical diagnosis, or may be prone to artifact that could lead to an equivocal other test, such as obese patients.”
While comparative studies were identified for SPECT compared to PET in the evaluation of coronary artery disease, the comparative data are still limited. Using a thorax-cardiac phantom, Knesaurek and Machac concluded that PET was better at detecting smaller defects. In this study, a 1-cm insert was not detectable by SPECT yet it was detectable using PET. Merhige and colleagues reported on outcomes of non-contemporaneous patients with similar probabilities of coronary artery disease that were evaluated by SPECT or PET. In this study involving PET scans done at one center compared to those evaluated by SPECT, those receiving PET evaluations had lower rates of angiography (13% versus 31%) and revascularization (6% and 11%) with similar rates of death and myocardial infarction at one year of follow-up. These results are viewed as preliminary and additional comparative studies showing impact on outcomes are needed. Another publication also described the PAREPET study that will determine whether the amount of viable dysfunctional myocardium and/or sympathetic dysinnervation is associated with the risk of sudden cardiac death.
A review by Di Carli and Hachamovitch describes the current and potential diagnostic uses of cardiac PET and is in agreement with the policy statements. The Study of Perfusion and Anatomy’s Role in CAD (SPARC) trial is recruiting patients to evaluate the role of cardiac PET/CT for the diagnosis of coronary artery disease. To date, there are no articles from the PAREPET or SPARC trials.
Recent review articles discuss the potential applications for PET in various neurological and psychological conditions. Henry and Van Heertum recently suggested that “interictal FDG PET can be used in presurgical epilepsy evaluations to reliably: 1) determine the side of anterior temporal lobectomy, and in children the area of multilobar resection, without intracranial electroencephalographic recording of seizures; 2) select high-probability sites of intracranial electrode placement for recording ictal onsets; and 3) determine the prognosis for complete seizure control following anterior temporal lobe resection.” The performance data for PET localization of seizure foci has already been established. It is suggested that FDG PET might also be used to localize and minimize the placement of intracranial electrodes that could reduce the morbidity associated with intracranial monitoring, even if invasive monitoring was not avoided altogether.
Parsey and Mann state that “brain imaging is not yet part of clinical practice in psychiatry,” and describe the various PET tracers and applications currently being investigated. PET radiotracers include the use of 18F-FDG to track metabolic activity, 15-O-water as a marker for cerebral blood flow, and a variety of 11-C tagged neuroreceptor markers to study serotonergic or dopaminergic activity as well as psychotropic drug effects.
The role of PET in dementia is an active area for research but is not yet clear. The Centers for Medicare and Medicaid Services (CMS) issued a decision memorandum on April 16, 2003, that would not support coverage of FDG PET in Alzheimer’s disease (AD) because the evidence did not demonstrate its use for improved patient outcomes. This decision was based, in part, on a technology assessment conducted at Duke University through the AHRQ Evidence-based Practice Center. This assessment used decision-analysis modeling to examine whether the use of FDG PET would improve health outcomes when used for diagnosis of AD in three clinical populations: patients with dementia, patients with mild cognitive impairment, or subjects with no symptoms but a first-degree relative with AD. PET was considered to have an 88% sensitivity (79% to 94% = 95% confidence interval [CI]) and 87% specificity (77% to 93% = 95% CI) for diagnosing AD. The report concluded that outcomes for all three groups of patients were better if all patients were treated with agents such as cholinesterase inhibitors rather than using FDG PET to select patients for treatment based on PET results, since the complications of treatment were relatively mild and treatment was considered to have some degree of efficacy in delaying the progression of AD. Thus, the adverse effect of not treating subjects with AD who had false-negative PET results was influential in this analysis. However, this conclusion was sensitive to the toxicity associated with treatment.
In October 2003, CMS accepted a petition from the University of California at Los Angeles (UCLA) School of Medicine to reconsider its policy for “use of FDG PET to distinguish patients with AD from those with other causes of symptoms confounding the diagnosis of dementia or to assist with the diagnosis of early dementia in beneficiaries for whom the differential diagnosis included one or more kinds of neurodegenerative disease, in cases where specific criteria have been met.” On September 15, 2004, Medicare made public its final decision memorandum announcing a positive national coverage decision for a subset of patients “with a recent diagnosis of dementia and documented cognitive decline of at least six months, who meet diagnostic criteria for both Alzheimer’s disease (AD) and frontotemporal dementia (FTD), who have been evaluated for specific alternative neurodegenerative diseases or causative factors, and for whom the cause of the clinical symptoms remains uncertain.”
For its reconsideration, CMS requested an update of the original AHRQ assessment. In addition, Medicare considered a consensus report by the Neuroimaging Work Group of the Alzheimer’s Association and proceedings of an expert panel discussion of neuroimaging in AD, convened by the National Institute of Aging and Medicare.
The updated technology assessment concluded that no new publications provided direct evidence to evaluate the use of PET to either differentiate among different types of dementia or to identify those patients with mild cognitive impairment who were at greatest risk to progress to AD.
The additional sources considered by Medicare, i.e., a consensus report, and an expert panel discussion, acknowledged the lack of direct evidence. However, these sources also suggested that, based on expert opinion, PET scanning potentially provided additional information in the small subset of patients presenting with diagnostic uncertainties between AD and FTD. It should be noted that the experts also expressed serious concerns about the potential misuse of PET scanning in patients with dementia, leading to unnecessary radiation exposure and costs.
In their decision memorandum, Medicare notes that they had previously indicated that they would consider “evidence from structured expert decision analysis of clinical scenarios…” in supporting coverage of such clinical indications. The salient points of the specific coverage criteria are summarized as follows:
“The evidence is adequate to conclude that an FDG-PET scan is reasonable and necessary in patients with a recent diagnosis of dementia and documented cognitive decline of at least six months, who meet diagnostic criteria for both Alzheimer’s disease (AD) and frontotemporal dementia (FTD), who have been evaluated for specific alternative neurodegenerative diseases or causative factors, and for whom the cause of the clinical symptoms remains uncertain. The following additional conditions must be met.
Medicare also notes that it intends to cover PET scans in "practical clinical trials" that are Medicare approved for studying the use of PET in dementia. Medicare indicated it will work with the National Institute on Aging (NIA), AHRQ, Alzheimer's Association (AA), and experts in AD and imaging to develop the trials.
In contrast to the CMS national policy, this medical policy continues to consider PET for AD and dementia as investigational, due to the lack of direct evidence that this imaging technique will result in a change in management that will improve patient outcomes.
A recent scientific statement from the AHA provides guidelines and recommendations for perfusion imaging in cerebral ischemia. The authors state that “although the development of these techniques has been fascinating, their role in evaluating a variety of diseases of the CNS [central nervous system] is controversial.” This report mentions that “oxygen extraction fraction (OEF) as measured with PET scanning” is being used in a new national trial to help “define the patient population with occlusive vascular disease at risk for stroke and the potential of an EC-IC [extracranial-intracranial] bypass to decrease that risk.” This report further states that “other types of perfusion imaging with challenge tests may act as surrogate techniques for the more elaborate and expensive PET-OEF technique.”
Two additional studies were identified exploring the use of FDG PET to assist in the differential diagnosis of infection in musculoskeletal conditions. Schmitz et al. evaluated 16 consecutive subjects with suspected spondylodiscitis on the basis of clinical and imaging findings who underwent surgical histopathological evaluation. Interpretation of FDG PET was blinded to clinical information and final diagnosis. This study reported that FDG PET was able to identify the presence of spondylodiscitis in all 12 subjects who had surgically proven infection (100% sensitivity). Among the four cases without evidence of infection at surgery, PET was truly negative in three cases with either degenerative changes or fracture and falsely positive in one patient who had a spinal sarcoma but no associated infection (75% specificity). A study by Manthey et al. explored the use of FDG-PET for differentiating synovitis, loosening, and infection in 23 patients who had 14 hip and 14 knee prostheses, but PET interpretations were not clearly blinded. Results found that PET identified four of four cases with periprosthetic infection and four of five cases with periprosthetic loosening, and there were true-negative PET results in three cases without evidence of infection, loosening, or synovitis. Confirmation of these favorable preliminary results in well-designed, prospective studies including larger numbers of patients is needed.
In a systematic review and meta-analysis of diagnostic imaging to assess chronic osteomyelitis, the authors reviewed studies through July 2003 on six imaging approaches to chronic osteomyelitis, including fluorodeoxyglucose PET. The study concluded that PET is the most accurate mode (pooled sensitivity = 96% [95% CI: 88%-99%]; pooled specificity = 91% [95% CI: 81%-95%]) for diagnosing chronic osteomyelitis. Leukocyte scintigraphy is adequate in the peripheral skeleton (sensitivity = 84% [95% CI: 72%-91%]; specificity = 80% [95%CI: 61%-91%]), but is inferior in the axial skeleton (sensitivity = 21% [95% CI: 11%-38%]; specificity = 60% [95%CI: 39%-78%]). The assessment of PET is based on four prospective, European studies published between 1998 and 2003, with a total of 1,660 patients. However, the study populations vary and include the following: 1) 57 patients with suspected spinal infection referred for FDG PET and who had previous spinal surgery, but not “recently;” 2) 22 trauma patients scheduled for surgery who had suspected metallic implant-associated infection; 3) 51 patients with recurrent osteomyelitis or osteomyelitis symptoms for more than six weeks, 36 in the peripheral skeleton and 15 in the central skeleton; and 4) 30 consecutive non-diabetic patients referred for possible chronic osteomyelitis. The results appear to be robust across fairly diverse clinical populations, which strengthen the conclusions. A clinical trial funded by the U.S. National Institutes of Health at the University of Pennsylvania to look at the use of FDG PET in the complicated diabetic foot started in 2002 and began enrolling patients in March 2007, toward a target of 240 patients. This trial may provide additional information on the use of PET in this specific population.
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The information contained in this section is for informational purposes only. HCSC makes no representation as to the accuracy of this information. It is not to be used for claims adjudication for HCSC Plans.
Medicare (CMS) does have a national coverage position.
A national coverage position for Medicare may have been developed or changed since this medical policy document was written. See Medicare's National Coverage at <http://www.cms.hhs.gov>.
Blue Cross Blue Shield Association Technology Evaluation Center (TEC) Assessments:
Positron Emission Tomography, July 1989, pages 155-183.
Positron Emission Tomography of the Heart, June 1991, pages 186-222.
Positron Emission Tomography (PET) of Central Nervous System Diseases, April 1992, pages 32-110.
Positron Emission Tomography for Assessment of Myocardial Viability, Volume 9, No.29, October 1994, pages 1-19.
Positron Emission Tomography for the Diagnosis of Cardiomyopathy, Volume 9, No. 30, October 1994, pages 1-10.
FDG Positron Emission Tomography for Non-CNS Cancer, Volume 10, No. 20, October 1995, pages 1-33.
PET Myocardial Perfusion Imaging for the Detection of Coronary Artery Disease - Clinical Assessment, Volume 10, No. 21, October 1995, pages 1-25.
PET, SPECT, or MRS in the Differential Diagnosis of Dementias, Volume 10, No. 29, April 1996, pages 1-15.
PET or SPECT in the Management of Seizure Disorders, Volume 11, No. 33, March 1997, pages 1-17.
PET or SPECT in the Diagnosis and Management of Brain Tumors, Volume 11, No. 34, March 1997, pages 1-25.
PET or SPECT for the Assessment of Cerebrovascular Disease, Volume 11, No. 35, March 1997, pages 1-29.
FDG Positron Emission Tomography for Non-CNS Cancers, Volume 12, No. 3, May 1997, pages 1-63.
PET Myocardial Perfusion Imaging for the Detection of Coronary Artery Disease - Cost Effectiveness Analysis, Special Assessment, 1998, pages 1-18.
FDG Positron Emission Tomography in Colorectal CA, Volume 14, No. 25, 4/2000.
FDG Positron Emission Tomography in Lymphoma, Volume 14, No. 26, 4/2000.
FDG Positron Emission Tomography in Melanoma, Volume 14, No. 27, 4/2000.
FDG Positron Emission Tomography in Pancreatic Cancer, Volume 14, No. 28.
FDG Positron Emission Tomography in Head and Neck Cancer, Volume 15, No. 4, 6/2000.
FDG Positron Emission Tomography for Evaluating Breast Cancer, Volume 16, No. 5, 8/2001
FDG Positron Emission Tomography for Evaluating Esophageal Cancer, Volume 16, No. 21, 4/2002.
FDG Positron Emission Tomography (PET) For the Detection of Ovarian Cancer. 6/2002.
FDG Positron Emission Tomography to Manage Patients with an Occult Primary Carcinoma and Metastasis Outside the Cervical Lymph Nodes, 6/2002.
Diamond GA, Forrester JS, Hirsch M et al. Application of conditional probability analysis to the clinical diagnosis of coronary artery disease. J Clin Invest 1980; 65(5):1210-21.
Ritchie JL, Bateman TM, et al. Guidelines for the clinical use of cardiac radionuclide imaging. Journal of the American College of Cardiology (1995) 25(2):521-47.
Guhlmann, A., Brecht-Krauss, D., et al. Fluorine-18-FDG PET and technetium-99m antigranulocyte antibody scintigraphy in chronic osteomyelitis. Journal of Nuclear Medicine (1998) 39(12):2145-52.
Neuroimaging Subcommission of the International League Against Epilepsy (ILAE). Commission on Diagnostic Strategies: recommendations for functional neuroimaging of persons with epilepsy. Epilepsia (2000) 41(10):1350-6.
de Winter, F., van de Wiele, C., et al. Fluorine-18 fluorodeoxyglucose-positron emission tomography: a highly accurate imaging modality for the diagnosis of chronic skeletal infections. Journal of Bone of Joint Surgery American Volume (2001) 83-A(5):651-60.
Siebelink, H.M., Blanksma, P.K., et al. No difference in cardiac event-free survival between positron emission tomography-guided and single-photon emission computed tomography-guided management: a prospective, randomized comparison of patients with suspicion of jeopardized myocardium. Journal of the American College of Cardiology (2001) 37(1):81-8.
Udelson, J.E. Testing our tests: surrogate end points versus driving patient management and outcomes. Journal of the American College of Cardiology (2001) 37(1):89-92.
Schmitz, A., Risse, J.H., et al. Fluorine-18 fluorodeoxyglucose positron emission tomography findings in spondylodiscitis: preliminary results. European Spine Journal (2001) 10(6):534-9.
Wallace, M.B., Nietert, P.J., et al. An analysis of multiple staging management strategies for carcinoma of the esophagus: Computed tomography, endoscopic ultrasound, positron emission tomography, and thoracoscopy/laparoscopy. Annals of Thoracic Surgery (2002) 74(4):1026-32.
Medicare Claims Manual, Rev. 113 (04-99), 50-36.
Medicare Policy: Program Memorandum, Coverage and Related Claims Processing Requirements for Positron Emission Tomography (PET) Scans –for Breast Cancer and Revised Coverage Conditions for Myocardial Viability, Transmittal AB-02-065, May 2, 2002. Accessible at <www.cms.hhs.gov>.
Manthey, N., Reinhard, P., et al. The use of [18F]fluorodeoxyglucose positron emission tomography to differentiate between synovitis, loosening and infection of hip and knee prostheses. Nuclear Medicine Community (2002) 23(7):645-53.
Meller, J., Koster, G., et al. Chronic bacterial osteomyelitis: prospective comparison of (18)F-FDG imaging with a dual-head coincidence camera and (111) ln-labelled autologous leucocyte scintigraphy. European Journal of Nuclear Medicine and Molecular Imaging (2002) 29(1):53-60.
FDG-PET Imaging in the Complicated Diabetic Foot. NCT00194298. Accessed at <www.clinicaltrials.gov> (accessed – 2007 March 30).
Ioannidis, J.P.A., and J. Lau. FDG-PET for the Diagnosis and Management of Soft Tissue Sarcoma (Technology Assessment). Rockville, MD: Agency for Healthcare Research and Quality (2002 April).
FDA Internet Bulletin Board (on-line), 02/98, The History and Evolution of PET, How PET Works, The Cyclotron and PET, Selected PET Resources on the Internet. <www.fda.gov>.
Gourgiotis, L., Sarlis, L., et al. Localization of medullary thyroid carcinoma metastasis in a multiple endocrine neoplasia type 2A patient by 6-[18F]-fluorodopamine positron emission tomography. Journal of Clinical Endocrinology and Metabolism (2003 February) 88(2):637-41.
Crippa, F., Gerali, A., et al. FDG-PET in thyroid cancer. Tumori (2003 September/October) 89(5):540-3.
Boer, A., Szakall, S. Jr., et al. FDG PET imaging in hereditary thyroid cancer. European Journal of Surgical Oncology (2003 December) 29(10):922-28.
Khan, N., Oriuchi, N., et al. PET in the follow-up of differentiated thyroid cancer. British Journal of Radiology (2003) 76, 690-95.
Schiesser, M., Stumpe, K.D., et al. Detection of metallic implant-associated infections with FDG PET in patients with trauma: correlation with microbiologic results. Radiology (2003) 226(2):391-8.
Klocke, F.J., Baird, M.G., et al. ACC/AHA/ASNC guidelines for clinical use of cardiac radionuclide imaging: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (ACC/AHA/ASNC Committee to Revise the 1995 Guidelines for the Clinical Use of Radionuclide Imaging) 2003 American College of Cardiology Web site. Available at <http://www.acc.org>.
Latchaw, R.E., Yonas, H., et al. Guidelines and recommendations for perfusion imaging in cerebral ischemia: a scientific statement for healthcare professionals by the Writing Group on Perfusion Imaging from the Council on Cardiovascular Radiology of the American Heart Association. Stroke (2003) 34(4):1084-104.
Parsey, R.V., and J.J. Mann. Applications of positron emission tomography in psychiatry. Seminars in Nuclear Medicine (2003) 33(2):129-35.
Visvanathan, R. PET imaging and dementia. Medical Science Monitor (2003) 9(4):RA96-100.
Henry, T.R., and R.L. Van Heertum. Positron emission tomography and single photon emission computed tomography in epilepsy care. Seminars in Nuclear Medicine (2003) 33(2):88-104.
Marchesi, M., Biffoni, M., et al. False-positive finding on 18F-FDG PET after chemotherapy for primary diffuse large B-cell lymphoma of the thyroid: a case report. Japan Journal of Clinical Oncology (2004 May) 34(5):280-1.
Gotthardt, M, Battmann, A, et al. 18F-FDG PET, somatostatin receptor scintigraphy, and CT in metastatic medullary thyroid cardinoma: a clinical study and an analysis of the literature. Nuclear Medicine Community (2004 May) 25(5):439-43.
Mansi, L., Moncayo, R., et al. Nuclear medicine in diagnosis, staging and follow-up of thyroid cancer. Quarterly Journal of Nuclear Medicine and Molecular Imaging (2004 June) 48(2):82-95.
Beyer, T., Gerald, A.M., et al. Acquisition Protocol Considerations for Combined PET/CT Imaging. The Journal of Nuclear Medicine (2004 January) 45(1): (Supplement).
Screening for Dementia: Recommendation and Rationale, American Family Physician. U.S. Preventive Services Task Force (2004 March 15).
Patwardhan, M.B., McCrory, D.C., et al. Alzheimer disease: operating characteristics of PET—a meta-analysis. Radiology (2004 April) 231(1):73-80.
Verchakelen, J., De Wever, W., et al. Role of Computed Tomography in Lung Cancer Staging. Current Opinion Pulmonary Medicine (2004) 10(4):248-55.
Matcher, D.B., Kulasingam, S.L., et al. Technology Assessment. Positron emission tomography, single photon emission computed tomography, computed tomography, functional magnetic resonance imaging, and magnetic resonance spectroscopy for the diagnosis and management of Alzheimer’s dementia. Duke Center for Clinical Policy Research and Evidence Practice Center. (2004 April). Available at <http://www.cms.hhs.gov>.
Neuroimaging Work Group, Alzheimer’s Association. The use of MRI and PET for clinical diagnosis of dementia & investigation of cognitive impairment: a consensus report (2004). Available at <http://www.alz.org>.
Neuroimaging in the diagnosis of Alzheimer’s disease and dementia. Expert panel convened by the Neuroscience and Neuropsychology of Aging Program, National Institute of Aging (NIA), DHHS and the Centers for Medicare and Medicaid Services (CMS), DHHS (2004 April 5). Available at <http://www.cms.hhs.gov>.
Matchar, D.B., Kulasingam, S.L., et al. Positron Emission Testing for Six Cancers (Brain, Cervical, Small Cell Lung, Ovarian, Pancreatic and Testicular), (Technology Assessment). Rockville, MD: Agency for Healthcare Research and Quality (2004 February).
Termaat, M.F., Raijmakers, P.G., et al. The accuracy of diagnostic imaging for the assessment of chronic osteomyelitis: a systematic review and meta-analysis. Journal of Bone and Joint Surgery American Volume (2005) 87(11):2464-71.
Slart, R.H., Bax, J.J., et al. Comparison of 99mTc-sestamibi/18FDG DISA SPECT with PET for the detection of viability in patients with coronary artery disease and left ventricular dysfunction. European Journal of Nuclear Medicine and Molecular Imaging (2005) 32(8):972-9.
Isasi, C.R., Moadel, R.M., et al. A meta-analysis of FDG-PET for the evaluation of breast cancer recurrence and metastases. Breast Cancer Research and Treatment (2005) 90(2):105-12.
Sloka, J.S., Hollett, P.D., et al. Cost-effectiveness of positron emission tomography in breast cancer. Molecular Imaging Biology (2005) 7(5):351-60.
Westerterp, M., van Westreenen, H.L., et al. Esophageal cancer: CT, endoscopic US, and FDG PET for assessment of response to neoadjuvant therapy – systematic review. Radiology (2005) 236(3):841-51.
Seidenfeld, J., Samson, D., et al. Management of Small Cell Lung Cancer. Evidence Report.Publication No. 06-E016.Rockville, MD: Agency for Healthcare Research and Quality (2006 July).
Bateman TM, Heller GV, McGhie AI et al. Diagnostic accuracy of rest/stress ECG-gated Rb-82 myocardial perfusion PET: comparison with ECG-gated Tc-99m sestamibi SPECT. J Nucl Cardiology 2006; 13(1):24-33.
Beanlands RS, Chow BJ, Dick A et al. CCS/CAR/CANM/CNCS/CanSCMR joint position statement on advanced noninvasive cardiac imaging using positron emission tomography, magnetic resonance imaging and multidetector computed tomographic angiography in the diagnosis and evaluation of ischemic heart disease--executive summary. Can J Cardiol 2007; 23(2):107-19.
Oncologic Applications of PET Scanning. Chicago, Illinois: Blue Cross Blue Shield Association Medical Policy Reference Manual (2007 February) Radiology 6.01.26.
Miscellaneous Applications of Positron Emission Tomography (PET) Scanning. Chicago, Illinois: Blue Cross Blue Shield Association Medical Policy Reference Manual (2007 April) Radiology 6.01.06.
Di Carli MF, Hachamovitch R. New technology for noninvasive evaluation of coronary artery disease. Circulation 2007; 115(11):1464-80.
Cardiac Applications of PET Scanning. Chicago, Illinois: Blue Cross Blue Shield Association Medical Policy Reference Manual (2009 January) Radiology 6.01.20.
National Clinical Practice Guidelines in Oncology™, v1.2009. National Comprehensive Cancer Network. Available at <http://www.nccn.org> (Accessed – 2009 June).
Study of Perfusion and Anatomy's Role in CAD. ClinicalTrials.gov; NCT00321399.
(Available at http://www.clinicaltrials.gov- Accessed February 2009.)
10/1/2009 Revised/updated entire document
7/1/2009 Policy revised to allow coverage of PET for ovarian cancer, pancreatic cancer, small cell lung cancer, and soft tissue sarcoma.
3/1/2008 Revised/Updated Entire Document
2/1/2005 Revised/Updated Entire Document
10/16/2004 Revised/Updated Entire Document
10/2003 Codes Revised/Added/Deleted
8/1/2003 Revised/Updated Entire Document
5/2000 Codes Revised/Added/Deleted
1/2000 Codes Revised/Added/Deleted
9/1999 Codes Revised/Added/Deleted
4/1999 Codes Revised/Added/Deleted
5/1996 Codes Revised/Added/Deleted
10/1994 Codes Revised/Added/Deleted
10/1992 Codes Revised/Added/Deleted
7/1992 Codes Revised/Added/Deleted
1/1992 Codes Revised/Added/Deleted
5/1990 New Medical Document
|Title:||Effective Date:||End Date:|
|Cardiac Applications of Positron Emission Tomography Scanning||11-15-2018||04-30-2019|
|Cardiac Applications of Positron Emission Tomography Scanning||12-01-2017||11-14-2018|
|Positron Emission Tomography (PET)||04-15-2017||11-30-2017|
|Positron Emission Tomography (PET)||03-01-2016||04-14-2017|
|Positron Emission Tomography (PET)||10-15-2015||02-29-2016|
|Positron Emission Tomography (PET)||01-01-2014||10-14-2015|
|Positron Emission Tomography (PET)||01-01-2012||12-31-2013|
|Positron Emission Tomography (PET)||06-01-2011||12-31-2011|
|Positron Emission Tomography (PET)||06-15-2010||05-31-2011|
|Positron Emission Tomography (PET)||10-01-2009||06-14-2010|
|Positron Emission Tomography (PET)||07-01-2009||09-30-2009|
|Positron Emission Tomography (PET)||03-01-2008||06-30-2009|
|Positron Emission Tomography (PET)||02-01-2005||02-29-2008|
|Positron Emission Tomography (PET)||10-16-2004||01-31-2005|
|Positron Emission Tomography (PET)||08-01-2003||10-15-2004|