Skip to main content

Main menu

  • Home
  • Content
    • Current
    • Ahead of print
    • Past Issues
    • JNM Supplement
    • SNMMI Annual Meeting Abstracts
    • Continuing Education
    • JNM Podcasts
  • Subscriptions
    • Subscribers
    • Institutional and Non-member
    • Rates
    • Journal Claims
    • Corporate & Special Sales
  • Authors
    • Submit to JNM
    • Information for Authors
    • Assignment of Copyright
    • AQARA requirements
  • Info
    • Reviewers
    • Permissions
    • Advertisers
  • About
    • About Us
    • Editorial Board
    • Contact Information
  • More
    • Alerts
    • Feedback
    • Help
    • SNMMI Journals
  • SNMMI
    • JNM
    • JNMT
    • SNMMI Journals
    • SNMMI

User menu

  • Subscribe
  • My alerts
  • Log in
  • Log out
  • My Cart

Search

  • Advanced search
Journal of Nuclear Medicine
  • SNMMI
    • JNM
    • JNMT
    • SNMMI Journals
    • SNMMI
  • Subscribe
  • My alerts
  • Log in
  • Log out
  • My Cart
Journal of Nuclear Medicine

Advanced Search

  • Home
  • Content
    • Current
    • Ahead of print
    • Past Issues
    • JNM Supplement
    • SNMMI Annual Meeting Abstracts
    • Continuing Education
    • JNM Podcasts
  • Subscriptions
    • Subscribers
    • Institutional and Non-member
    • Rates
    • Journal Claims
    • Corporate & Special Sales
  • Authors
    • Submit to JNM
    • Information for Authors
    • Assignment of Copyright
    • AQARA requirements
  • Info
    • Reviewers
    • Permissions
    • Advertisers
  • About
    • About Us
    • Editorial Board
    • Contact Information
  • More
    • Alerts
    • Feedback
    • Help
    • SNMMI Journals
  • View or Listen to JNM Podcast
  • Visit JNM on Facebook
  • Join JNM on LinkedIn
  • Follow JNM on Twitter
  • Subscribe to our RSS feeds
Research ArticleClinical Investigations

Clinical Utility of Enhanced Relative Activity Recovery on Systolic Myocardial Perfusion SPECT: Lessons from PET

Danai Kitkungvan, Pimprapa Vejpongsa, Ketan P. Korrane, Stefano Sdringola and K. Lance Gould
Journal of Nuclear Medicine December 2015, 56 (12) 1882-1888; DOI: https://doi.org/10.2967/jnumed.115.153759
Danai Kitkungvan
Division of Cardiovascular Medicine, Department of Internal Medicine, University of Texas Health and Science Center at Houston, Houston, Texas
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Pimprapa Vejpongsa
Division of Cardiovascular Medicine, Department of Internal Medicine, University of Texas Health and Science Center at Houston, Houston, Texas
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Ketan P. Korrane
Division of Cardiovascular Medicine, Department of Internal Medicine, University of Texas Health and Science Center at Houston, Houston, Texas
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Stefano Sdringola
Division of Cardiovascular Medicine, Department of Internal Medicine, University of Texas Health and Science Center at Houston, Houston, Texas
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
K. Lance Gould
Division of Cardiovascular Medicine, Department of Internal Medicine, University of Texas Health and Science Center at Houston, Houston, Texas
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Abstract

SPECT and PET myocardial perfusion images show greater myocardial intensity and homogeneity in systole than diastole because of greater systolic myocardial thickness, less partial volume loss, and enhanced activity recovery. Consequently, conventional myocardial perfusion images obtained from whole cardiac cycles have lower myocardial intensity and greater heterogeneity than systolic images. Considering relative activity distribution on SPECT systolic images may add clinical utility to whole-cycle images and wall motion. Methods: Patients undergoing coronary angiogram within 4 mo after SPECT myocardial perfusion imaging were reviewed. Images were interpreted by 2 masked interpreters using a 17-segment, 5-point scale to determine summed rest scores (SSS), summed stress scores, and summed difference scores on conventional and systolic images in 603 patients (55.6% no coronary artery disease [no-CAD] and 44.4% CAD). Studies were considered normal when the SSS was less than 4 and summed difference score was less than 2. Results: In the no-CAD group, systolic SSS was lower than SSS from conventional images (2 ± 2.3 vs. 3 ± 2.6, P < 0.001). In contrast, SSS derived from systolic and conventional images were not different in the obstructive CAD group (9.1 ± 7.6 vs. 9.2 ± 7.4, P = 0.559). When systolic images were considered, true-negative studies increased from 27.2% to 43.3% (P < 0.001) whereas false-positive studies decreased from 28.4% to 12.3% (P < 0.001). True-positive (38% vs. 37.2%, P = 0.505) and false-negative studies (6.5% vs. 7%, P = 0.450) were not significantly changed. Diagnostic accuracy increased from 65.2% to 80.8% (P < 0.001). Conclusion: For gated SPECT myocardial perfusion imaging, when relative activity distribution on systolic images was considered, false-positive studies were reduced and diagnostic accuracy was improved.

  • systolic myocardial perfusion SPECT
  • ECG gated SPECT perfusion images
  • myocardial perfusion imaging
  • SPECT image artifact

SPECT myocardial perfusion imaging (MPI) for evaluation of coronary artery disease (CAD) is well established and widely used (1,2). However, SPECT MPI is potentially subject to attenuation, partial-volume loss, and imaging artifacts due to contractile motion (3–5). Despite advances in SPECT MPI, imaging artifacts may lead to false-positive studies and difficulty differentiating true perfusion defects from artifacts in some patients (3–5).

Most SPECT MPI studies are now performed using electrocardiographic gating (6,7) that provides significant clinical information on left ventricular (LV) ejection fraction, wall thickening, and regional wall motion to augment SPECT MPI interpretation (8–10). However, routine interpretation of myocardial perfusion images and their summed stress scoring uses conventional whole-cycle images acquired during the entire cardiac cycle not separate systolic or diastolic gated perfusion images (7–11).

Because diastole comprises two thirds of the cardiac cycle, images acquired during diastole might be expected to have more influence on the conventional whole-cycle images than systolic images. However, diastolic images have substantially less myocardial intensity and count density than systolic images (12–15). For electrocardiography (ECG)-gated myocardial perfusion images even by high-resolution PET, systolic images have significantly greater quantitative recovery of absolute myocardial activity due to less partial-volume loss of the thicker systolic LV wall compared with diastolic wall thickness (14–17).

Similar to PET, in gated SPECT MPI, differences between systolic and diastolic quantitative recovery of myocardial activity arise from greater partial-volume loss caused by thinner diastolic LV wall thickness than in systole relative to the limited resolution of SPECT scanners that affects conventional whole-cycle perfusion images (12,17–20). Moreover, even in healthy subjects, myocardial perfusion images have regional variability due to varying LV wall thickness caused by papillary muscles, myocardial fiber orientation, and angled imaging planes (21–24). Therefore, the lower diastolic count recovery, compared with systole, can produce or potentiate image inhomogeneity that may appear as perfusion defects in conventional whole-cycle images of healthy subjects that improve or normalize on systolic images (25,26).

Cardiac translational motion in fixed imaging planes of the scanner also causes a complex difference between systolic and diastolic images, as demonstrated in Figure 1. Normally in systole, the heart and aortic root recoil downward and medially with LV ejection and move upward in diastole (27–29). As a consequence, the apex and inferior wall commonly descend into the distal inferior imaging plane in systole and move up out of this plane in diastole (14,29–31). This translational motion may leave the distal inferior imaging plane with less activity during diastole, thereby creating artifactual defects in conventional whole-cycle images that are not present on systolic images, as documented on prior ECG-gated PET studies (14,29–31).

FIGURE 1.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIGURE 1.

Medial and downward recoil of left ventricle during systole may move inferior myocardium into and out of the most inferior imaging plane, thereby reducing inferior activity, especially for inferior apex, with resulting artifact in conventional whole-cycle images not present on systolic images.

LV wall motion on ECG-gated perfusion images is commonly used to help differentiate myocardial scar or ischemia from attenuation artifact (8–10). However, our purpose was to test the potential added clinical utility of considering relative activity distribution on systolic images in addition to relative activity and wall motion on standard gated whole-cycle images. Quantitative measurements by ECG-gated PET have proven that systolic perfusion images have quantitatively significantly reduced partial-volume loss and better quantitative activity recovery than diastolic or whole-cycle images (14,29–31). Therefore, for SPECT perfusion imaging, we tested the hypothesis that interpreting relative activity distribution of systolic images would decrease the number of false-positive studies because of reduced partial-volume loss and reduced translational motion on systolic images, thereby improving diagnostic accuracy.

MATERIALS AND METHODS

Patient Selection

From January 2010 to December 2013, all sequential patients who underwent stress and rest gated SPECT MPI with 99mTc-sestamibi at Memorial Hermann Hospital, Texas Medical Center, were reviewed. Patients who had a coronary angiogram within 4 mo after gated SPECT MPI were included in the study. The Committees for the Protection of Human Subjects (institutional review board) of the University of Texas and Memorial Hermann Hospital approved the project and determined that signed patient consent for data analysis was not necessary because only deidentified data were used from existing medical records.

Patients with nonischemic cardiomyopathy, previous coronary revascularization, or an interim event were excluded from the study because perfusion defects in these groups may not correlate with the result of coronary angiogram at the time they were performed (9,32). As reported for virtually all MPI–angiogram comparisons in the literature and routine clinical practice, patients were considered to have CAD when the angiogram showed 50% or greater stenosis of the left main coronary artery or a 70% or greater stenosis of other epicardial coronary arteries by visual interpretation as entered into the official angiogram report.

Imaging Protocols and Interpretation

All images were acquired according to the guidelines of the American Society of Nuclear Cardiology (ASNC) using ECG-gated (8 frames per R-R cycle) SPECT single-day or 2-d (depending on body weight) protocols (7). In our institution, only stress images are gated. All γ cameras were dual-detector systems, with a 90° orientation (7). Images were reconstructed primarily by filtered backprojection with a Butterworth prefilter; power of 10; critical frequency of 0.45 Nq for stress, 0.4 Nq for rest images, and 0.35 Nq for ECG-gated images at rest and stress; and, less commonly, a quantitative ramp filter or ordered-subset expectation maximization/maximum likelihood expectation maximization, 2 iterations, subset 10, and the same filters.

Stress was performed by standard exercise treadmill (Bruce or modified Bruce protocol), adenosine infusion (4-min intravenous infusion at a dose of 140 mcg/kg/min with or without slow-paced walk on treadmill), regadenoson (single 400-mcg intravenous bolus), or dobutamine infusion (intravenous infusion at 5–40 mcg/kg/min) (6).

SPECT myocardial perfusion images were interpreted by 2 masked interpreters using the ASNC 17-segment and 5-point qualitative scale (0, normal; 1, equivocal or mildly reduced; 2, moderately reduced; 3, severely reduced radioisotope uptake; and 4, absence of tracer uptake) to determine a consensus of summed rest score (SRS) and summed stress score (SSS) on conventional whole-cycle images (7). Summed difference score (SDS) is the difference of SSS and SRS indicating reversibility of perfusion defect (7).

In addition, gated stress images were navigated to the single end-systolic frame with the visually smallest LV cavity to calculate systolic SSS and SDS (systolic SSS − SRS). Occasionally for small hearts, the LV cavity nearly disappears as the end systolic frame for analysis. There was no additional training provided to interpreters for systolic image interpretation, who interpreted systolic images as if they were interpreting conventional images. Conventional whole-cycle images and systolic images were considered normal when SSS was less than 4 and SDS was less than 2 (7). LV regional wall motion and thickening were not used for determining SSS and SDS, consistent with ASNC guidelines.

Statistical Analysis

Demographic and patient characteristics were summarized according to the presence or absence of obstructive CAD using descriptive statistics (mean ± SD) for continuous variables and frequency (%) for categoric variables. Data were compared using unpaired and paired t tests where indicated for continuous variables. A 2-tailed Fisher exact test and McNemar χ2 test were used to compare paired categoric variables. P values of less than 0.05 indicated statistical significance.

RESULTS

During the study period, 4,564 sequential patients underwent SPECT MPI at our institution. After inclusion and exclusion criteria were applied, 603 patients meeting criteria were included in our study. The mean age was 57.5 ± 11.8 y, and 366 patients (60.7%) were men. Pharmacologic stress with intravenous adenosine infusion was used in 529 patients (87.7%), exercise treadmill stress in 52 patients (8.6%), and regadenoson in16 patients (2.7%). Baseline patient characteristics, risk factors for CAD, and type of stress test are described in Table 1. Significant obstructive CAD by angiography was found in 268 patients (44.4%). Among patients with CAD (Table 2), single-vessel disease was reported in 147 patients (54.9%), and the left anterior descending artery was the most commonly affected (165 patients, 61.6%).

View this table:
  • View inline
  • View popup
TABLE 1

Baseline Patient Characteristics

View this table:
  • View inline
  • View popup
TABLE 2

Coronary Artery Distribution in Patients with Obstructive CAD

Figure 2 shows schematic plots of scanner activity recovery across sections of short-axis images for conventional whole-cycle and systolic images in an example patient with normal coronary artery and no other obvious source of imaging artifact. Because of limited scanner resolution and efficiency at heart depth and associated partial-volume loss, the scanner failed to recover true activity (red dashed line) particularly more so causing relative perfusion defects in anterior and inferior walls in this example. In systole, the LV walls are thicker throughout the heart, with better activity recovery by the scanner and more homogeneous images than the conventional whole-cycle images such that the anterior defect normalizes on systolic images (Fig. 2A).

FIGURE 2.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIGURE 2.

In this example with normal angiogram, red dashed line indicates schematically true activity that scanners typically do not recover because of limited resolution and efficiency. Scanner activity recovery in anterior and inferior walls is less on conventional whole-cycle images than systolic images because of limited scanner resolution and partial-volume loss for diastolic images or cardiac motion. This difference between systolic and conventional whole-cycle relative images is less prominent for lateral walls because of their greater thickness due to papillary muscles and associated better activity recovery. (A) In systole, LV walls are thickened with better activity recovery by scanner such that anterior defect normalizes on systolic images, suggesting that defect on conventional image is artifact due to partial-volume loss. (B) Activity recovery profiles for inferior wall during systole compared with anterior defect. This inferior defect also substantially improves to nearly normal on systolic images, suggesting that defect in whole-cycle image is artifact. Some residual attenuation is likely due to diaphragm and liver.

The inferior defect has similar but less complete activity recovery profiles compared with the anterior defect (Fig. 2B), as expected because of diaphragmatic and liver attenuation. Nonetheless, both these defects substantially improve to nearly normal on systolic images, thereby suggesting that the defects seen in conventional images of this example are artifacts, as confirmed by a normal angiogram.

Examples of conventional whole-cycle and systolic image interpretation are demonstrated in Figure 3. Figure 3A illustrates short-axis views of an anterior stress perfusion defect on conventional whole-cycle images not present on the systolic images, suggesting that the defect on the whole-cycle image is an artifact, confirmed by coronary angiogram. Figure 3B illustrates an inferior stress defect on both the conventional whole-cycle and the systolic images, suggesting a true defect, confirmed by corresponding stenosis on coronary angiogram.

FIGURE 3.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIGURE 3.

(A) Anterior stress perfusion defect on whole-cycle image not present on systolic images suggesting that defect on whole-cycle image is artifact as confirmed by normal coronary angiogram. (B) Inferior stress perfusion defect on both whole-cycle and systolic images indicating true perfusion defect as confirmed by coronary angiogram.

Quantitative Scores of Perfusion Defects

All calculated SRS, SSS, and SDS were significantly lower in patients with no significant CAD as demonstrated in Table 3. LV ejection fraction in this group of patients was higher than those with CAD (61.6% ± 9.8% vs. 50.6% ± 15.8%, P < 0.001). In patients with no CAD, systolic SSS (Table 4) were significantly lower than SSS calculated from conventional whole-cycle images (2 ± 2.3 vs. 3 ± 2.6, P < 0.001). On the other hand (Table 4), the SSS derived from systolic and conventional whole-cycle images were not different in patients with significant CAD (9.1 ± 7.6 vs. 9.2 ± 7.4, P = 0.559). On average (Table 4), SSS calculated from systolic images were lower than those of conventional whole-cycle images by 1.0 ± 1.2 in patients with no CAD and by 0.1 ± 1.3 in patients with obstructive CAD (P < 0.001).

View this table:
  • View inline
  • View popup
TABLE 3

Interpretation Result by Conventional and Systolic Images in Patients With and Without CAD

View this table:
  • View inline
  • View popup
TABLE 4

SSS by Conventional and Systolic Images in Patients With and Without CAD

Integration of systolic images with gated SPECT MPI interpretation (Fig. 4) increased the number of true-negative studies from 164 (27.2%) to 261 (43.3%, P < 0.001) whereas false-positive studies decreased from 171 (28.4%) to 74 (12.3%, P < 0.001). In patients with obstructive CAD, the number of true-positive and false-negative studies was not significantly changed by adding systolic image interpretation (Fig. 4). Overall, diagnostic accuracy increased from 65.2% to 80.8% (P < 0.001) when systolic images were incorporated into image analysis (Fig. 4).

FIGURE 4.
  • Download figure
  • Open in new tab
  • Download powerpoint
FIGURE 4.

Bar graph demonstrates result of considering systolic images in interpretation of whole-cycle conventional images compared with coronary angiogram.

The consideration of systolic images did not change interpretation of conventional whole-cycle images (from abnormal to normal or normal to abnormal) in most patients (499 patients, 82.8%), as demonstrated in Table 5. For patients with baseline SSS greater than 8, none of the conventional whole-cycle image interpretations was altered by adding systolic image analysis (Table 5). Among 104 patients (17.2%) with conventional whole-cycle image interpretation altered by adding systolic images, the changed interpretations by considering systolic images correlated with their angiographic data were as follows: false-positive to true-negative in 97 patients (93.3%), true-positive to false-negative in 5 patients (4.8%), and false-negative to true-positive in 2 patients (1.9%).

View this table:
  • View inline
  • View popup
TABLE 5

Image Interpretation by Conventional and Systolic Images Based on Baseline SSS

In 97 studies in which interpretation changed from false-positive to true-negative, 31 patients (32%) had SSS less than 4 (mean SSS of 2.6 ± 0.5) but were considered to be abnormal by conventional whole-cycle images due to SDS of 2 or greater (mean SDS of 2.2 ± 0.4). In 5 studies that changed from true-positive to false-negative, the mean SSS and SDS with conventional method were 3.4 ± 0.9 and 1.6 ± 1.1, respectively, and 1.8 ± 1.3 and 0 ± 1.2, respectively, with added analysis of systolic images.

DISCUSSION

In our study, perfusion defects on systolic images, as measured by SSS, in patients without obstructive CAD were less severe and smaller than on conventional whole-cycle images because of greater homogeneity and enhanced activity recovery associated with less partial-volume loss and less motion artifact on systolic images. By contrast, in patients with obstructive CAD, there was no significant difference in the interpreted size or severity by SSS of perfusion defects between systolic and conventional whole-cycle images. These data suggest that artifactual perfusion defects in healthy subjects tend to improve or normalize on systolic images whereas true perfusion abnormalities in patients with obstructive CAD remain unchanged on systolic images. Incorporating systolic images into our routine SPECT MPI analysis improved clinical interpretation by decreasing the number of false-positive studies and increasing true-negative studies and improved overall diagnostic accuracy.

In our study, systolic images altered 32% of SPECT MPI clinical interpretation from false-positive to true-negative studies based on perfusion defects that normalized on systolic images despite being reversible on conventional rest–stress images. Systole comprises one third of the heart cycle at slow heart rates of resting conditions. At higher heart rates during vasodilator or exercise stress, systole comprises half or more of the cardiac cycle. Accordingly, as previously published in detail for quantitative PET perfusion imaging (14), systolic images have greater impact on whole-cycle images during tachycardia of stress, compared with the slower heart rates at resting conditions. Therefore, SDSs parallel the SSSs.

Systolic image interpretation is most useful and beneficial when perfusion defects are mild because systolic images did not alter interpretation of conventional whole-cycle images when SSS was 8 or greater. Our data indicate that considering systolic images is particularly useful for separating true perfusion abnormalities from motion artifacts for these mild perfusion defects, as confirmed by coronary angiogram.

Although not statistically significant, in a small number of patients (4.8% in our study) with small mild stress perfusion defects, systolic image interpretation might cause false-negative results. However, with or without additional information from systolic images, coronary intervention may not be beneficial or indicated in these patients because of small areas of mild myocardial ischemia. With this qualification, the use of systolic images in SPECT MPI interpretation substantially reduced false-positive studies at the small expense of a slight, statistically insignificant increase in number of false-negative studies.

We acknowledge several limitations in our study. Our study is a retrospective, case-control design that cannot account for unmeasured confounders. It was not designed to evaluate sensitivity and specificity of the SPECT MPI compared with coronary angiogram because referral bias could not be objectively considered (33,34). As a university quaternary care center, referral bias or unrecognized confounders likely affected our observed percentage of false-positive and false-negative images but their change by considering systolic images remains valid. Moreover, our observed 28% false-positive whole-cycle SPECT perfusion images compares with the average of 24% reported in a large recent meta-analysis with a range of false-positives up to 44%–53% in current practice (35,36).

Although only stress images were ECG-gated for systolic analysis in this study, comparing ECG-gated resting systolic images with stress systolic images would be expected to reduce artifacts of rest–stress change even more than reported here because the systolic rest images also have thicker LV walls and less partial-volume loss than diastolic or whole-cycle rest images. Whatever small differences in processing between gated and ungated images are unlikely to affect our results because the same gated–ungated processing differences applied to the definite stress defects on systolic and diastolic images confirmed by angiogram were also applied to stress defects that normalized on systolic images in patients with no stenosis on angiogram.

Despite our awareness of and our many publications on its limitations, visual interpretation of coronary stenosis on angiogram was used as a reference standard for binary classification of our study population into significant or nonsignificant coronary artery stenosis, similar to all previous reports on diagnostic accuracy of SPECT MPI in the literature and in widespread clinical practice (37,38).

Although our daily clinical interpretations incorporate wall motion and thickening on gated images, ASNC and American College of Cardiology protocols for qualitative SSS use relative defects without modification of the SSS by wall motion or thickening. Moreover, the literature reports no methodology for incorporating wall motion and thickening into SSS of relative perfusion defects.

Separately and in addition to the clinical use of wall motion and thickening, our study addresses the value of considering relative activity distribution on systolic images having enhanced activity uptake with corresponding greater homogeneity and intensity without motion artifacts due to ECG-gated acquisition. Therefore, as similar to all prior reports on SSS in MPI, our study did not incorporate regional LV wall motion and thickening to our whole-cycle SPECT MPI SSS (8–10,39,40). Interestingly, considering systolic stress scores provides a potential methodology for semiquantitatively incorporating ECG-gated data into interpretation of relative myocardial perfusion images.

CONCLUSION

Our study demonstrates that myocardial perfusion defects on conventional whole-cycle SPECT images that visually normalize on systolic images quantified by SSS are artifacts documented by correlation with coronary angiogram. Therefore, integrating relative activity distribution on systolic images combined with interpretation of conventional whole-cycle stress SPECT perfusion images reduces false-positive results with no significant increase in false-negatives and improves overall diagnostic accuracy, thereby potentially reducing the need for diagnostic coronary angiograms.

DISCLOSURE

The costs of publication of this article were defrayed in part by the payment of page charges. Therefore, and solely to indicate this fact, this article is hereby marked “advertisement” in accordance with 18 USC section 1734. K. Lance Gould receives internal funding from the Weatherhead PET Center for Preventing and Reversing Atherosclerosis endowment. He is also the 510(k) applicant for cfrQuant approved by the Food and Drug Administration. He has arranged that all his royalties permanently go to a University of Texas (UT) scholarship fund. UT has a commercial nonexclusive agreement with Positron Corporation to distribute and market cfrQuant in exchange for royalties. However, K. Lance Gould retains the ability to distribute cost-free versions to selected collaborators for research. Additionally, he has signed a nonfinancial, mutual nondisclosure agreement with Volcano Corporation (maker of FFR pressure wires) to discuss coronary physiology projects. No other potential conflict of interest relevant to this article was reported.

Footnotes

  • Published online Aug. 13, 2015.

  • © 2015 by the Society of Nuclear Medicine and Molecular Imaging, Inc.

REFERENCES

  1. 1.↵
    1. Hendel RC,
    2. Berman DS,
    3. Di Carli MF,
    4. et al
    . ACCF/ASNC/ACR/AHA/ASE/SCCT/SCMR/SNM 2009 appropriate use criteria for cardiac radionuclide imaging. J Am Coll Cardiol. 2009;53:2201–2229.
    OpenUrlCrossRefPubMed
  2. 2.↵
    1. Wolk MJ,
    2. Bailey SR,
    3. Doherty JU,
    4. et al
    . ACCF/AHA/ASE/ASNC/HFSA/HRS/SCAI/SCCT/SCMR/STS 2013 multimodality appropriate use criteria for the detection and risk assessment of stable ischemic heart disease. J Am Coll Cardiol. 2014;63:380–406.
    OpenUrlCrossRefPubMed
  3. 3.↵
    1. Case JA,
    2. Bateman TM
    . Taking the perfect nuclear image: quality control, acquisition, and processing techniques for cardiac SPECT, PET, and hybrid imaging. J Nucl Cardiol. 2013;20:891–907.
    OpenUrlCrossRefPubMed
  4. 4.
    1. Burrell S,
    2. MacDonald A
    . Artifacts and pitfalls in myocardial perfusion imaging. J Nucl Med Technol. 2006;34:193–211.
    OpenUrlAbstract/FREE Full Text
  5. 5.↵
    1. Dvorak RA,
    2. Brown RK,
    3. Corbett JR
    . Interpretation of SPECT/CT myocardial perfusion images: common artifacts and quality control techniques. Radiographics. 2011;31:2041–2057.
    OpenUrlCrossRefPubMed
  6. 6.↵
    1. Henzlova MJ,
    2. Cerqueira MD,
    3. Mahmarian JJ,
    4. Yao SS
    . Stress protocols and tracers. J Nucl Cardiol. 2006;13:e80–e90.
    OpenUrlCrossRefPubMed
  7. 7.↵
    1. Holly TA,
    2. Abbott BG,
    3. Al-Mallah M,
    4. et al
    . Single photon-emission computed tomography. J Nucl Cardiol. 2010;17:941–973.
    OpenUrlCrossRefPubMed
  8. 8.↵
    1. Smanio PE,
    2. Watson DD,
    3. Segalla DL,
    4. et al
    . Value of gating of technetium-99m sestamibi single-photon emission computed tomographic imaging. J Am Coll Cardiol. 1997;30:1687–1692.
    OpenUrlCrossRefPubMed
  9. 9.↵
    1. Go V,
    2. Bhatt MR,
    3. Hendel RC
    . The diagnostic and prognostic value of ECG-gated SPECT myocardial perfusion imaging. J Nucl Med. 2004;45:912–921.
    OpenUrlAbstract/FREE Full Text
  10. 10.↵
    1. Lima RS,
    2. Watson DD,
    3. Goode AR,
    4. et al
    . Incremental value of combined perfusion and function over perfusion alone by gated SPECT myocardial perfusion imaging for detection of severe three-vessel coronary artery disease. J Am Coll Cardiol. 2003;42:64–70.
    OpenUrlCrossRefPubMed
  11. 11.↵
    1. Paul AK,
    2. Nabi HA
    . Gated myocardial perfusion SPECT: basic principles, technical aspects, and clinical applications. J Nucl Med Technol. 2004;32:179–187.
    OpenUrlAbstract/FREE Full Text
  12. 12.↵
    1. Fukuchi K,
    2. Uehara T,
    3. Morozumi T,
    4. et al
    . Quantification of systolic count increase in technetium-99m-MIBI gated myocardial SPECT. J Nucl Med. 1997;38:1067–1073.
    OpenUrlAbstract/FREE Full Text
  13. 13.
    1. Galt JR,
    2. Garcia EV,
    3. Robbins WL
    . Effects of myocardial wall thickness on SPECT quantification. IEEE Trans Med Imaging. 1990;9:144–150.
    OpenUrlCrossRefPubMed
  14. 14.↵
    1. Johnson NP,
    2. Sdringola S,
    3. Gould KL
    . Partial volume correction incorporating Rb-82 positron range for quantitative myocardial perfusion PET based on systolic-diastolic activity ratios and phantom measurements. J Nucl Cardiol. 2011;18:247–258.
    OpenUrlCrossRefPubMed
  15. 15.↵
    1. Yamashita K,
    2. Tamaki N,
    3. Yonekura Y,
    4. et al
    . Quantitative analysis of regional wall motion by gated myocardial positron emission tomography: validation and comparison with left ventriculography. J Nucl Med. 1989;30:1775–1786.
    OpenUrlAbstract/FREE Full Text
  16. 16.
    1. Hoffman EJ,
    2. Huang SC,
    3. Phelps ME
    . Quantitation in positron emission computed tomography: 1. Effect of object size. J Comput Assist Tomogr. 1979;3:299–308.
    OpenUrlCrossRefPubMed
  17. 17.↵
    1. Bartlett ML,
    2. Buvat I,
    3. Vaquero JJ,
    4. et al
    . Measurement of myocardial wall thickening from PET/SPECT images: comparison of two methods. J Comput Assist Tomogr. 1996;20:473–481.
    OpenUrlCrossRefPubMed
  18. 18.
    1. Pretorius PH,
    2. King MA
    . Diminishing the impact of the partial volume effect in cardiac SPECT perfusion imaging. Med Phys. 2009;36:105–115.
    OpenUrlCrossRefPubMed
  19. 19.
    1. Smith WH,
    2. Kastner RJ,
    3. Calnon DA,
    4. et al
    . Quantitative gated single photon emission computed tomography imaging: a counts-based method for display and measurement of regional and global ventricular systolic function. J Nucl Cardiol. 1997;4:451–463.
    OpenUrlCrossRefPubMed
  20. 20.↵
    1. Hutton BF,
    2. Osiecki A
    . Correction of partial volume effects in myocardial SPECT. J Nucl Cardiol. 1998;5:402–413.
    OpenUrlCrossRefPubMed
  21. 21.↵
    1. Pretorius PH,
    2. Pan TS,
    3. Narayanan MV,
    4. King MA
    . A study of the influence of local variations in myocardial thickness on SPECT perfusion imaging. IEEE Trans Nucl Sci. 2002;49:2304–2308.
    OpenUrlCrossRef
  22. 22.
    1. Bogaert J,
    2. Rademakers FE
    . Regional nonuniformity of normal adult human left ventricle. Am J Physiol Heart Circ Physiol. 2001;280:H610–H620.
    OpenUrlAbstract/FREE Full Text
  23. 23.
    1. Ho SY
    . Anatomy and myoarchitecture of the left ventricular wall in normal and in disease. Eur J Echocardiogr. 2009;10:iii3–iii7.
    OpenUrlCrossRef
  24. 24.↵
    1. Chareonthaitawee P,
    2. Kaufmann PA,
    3. Rimoldi O,
    4. Camici PG
    . Heterogeneity of resting and hyperemic myocardial blood flow in healthy humans. Cardiovasc Res. 2001;50:151–161.
    OpenUrlAbstract/FREE Full Text
  25. 25.↵
    1. Bartlett ML,
    2. Bacharach SL,
    3. Voipio-Pulkki LM,
    4. Dilsizian V
    . Artifactual inhomogeneities in myocardial PET and SPECT scans in normal subjects. J Nucl Med. 1995;36:188–195.
    OpenUrlAbstract/FREE Full Text
  26. 26.↵
    1. Gewirtz H,
    2. Tawakol A,
    3. Bacharach SL
    . Heterogeneity of myocardial blood flow and metabolism: review of physiologic principles and implications for radionuclide imaging of the heart. J Nucl Cardiol. 2002;9:534–541.
    OpenUrlCrossRefPubMed
  27. 27.↵
    1. Pratt RC,
    2. Parisi AF,
    3. Harrington JJ,
    4. Sasahara AA
    . The influence of left ventricular stroke volume on aortic root motion: an echocardiographic study. Circulation. 1976;53:947–953.
    OpenUrlAbstract/FREE Full Text
  28. 28.
    1. Beller CJ,
    2. Labrosse MR,
    3. Thubrikar MJ,
    4. Robicsek F
    . Role of aortic root motion in the pathogenesis of aortic dissection. Circulation. 2004;109:763–769.
    OpenUrlAbstract/FREE Full Text
  29. 29.↵
    1. Loghin C,
    2. Sdringola S,
    3. Gould KL
    . Common artifacts in PET myocardial perfusion images due to attenuation-emission misregistration: clinical significance, causes, and solutions. J Nucl Med. 2004;45:1029–1039.
    OpenUrlAbstract/FREE Full Text
  30. 30.
    1. Gould KL,
    2. Pan T,
    3. Loghin C,
    4. Johnson N,
    5. Guha A,
    6. Sdringola S
    . Frequent diagnostic errors in cardiac PET-CT due to misregistration of CT attenuation and emission PET images: a definitive analysis of causes, consequences and corrections. J Nucl Med. 2007;48:1112–1121.
    OpenUrlAbstract/FREE Full Text
  31. 31.↵
    1. Johnson NP,
    2. Pan T,
    3. Gould KL
    . Shifted helical CT to optimize cardiac PET-CT co-registration: quantitative improvement and limitations. Mol Imaging. 2010;9:256–267.
    OpenUrlPubMed
  32. 32.↵
    1. Danias PG,
    2. Ahlberg AW,
    3. Clark BA 3rd.,
    4. et al
    . Combined assessment of myocardial perfusion and left ventricular function with exercise technetium-99m sestamibi gated single-photon emission computed tomography can differentiate between ischemic and nonischemic dilated cardiomyopathy. Am J Cardiol. 1998;82:1253–1258.
    OpenUrlCrossRefPubMed
  33. 33.↵
    1. Ladapo JA,
    2. Blecker S,
    3. Elashoff MR,
    4. et al
    . Clinical implications of referral bias in the diagnostic performance of exercise testing for coronary artery disease. J Am Heart Assoc. 2013;2:e000505.
    OpenUrlAbstract/FREE Full Text
  34. 34.↵
    1. Miller TD,
    2. Hodge DO,
    3. Christian TF,
    4. et al
    . Effects of adjustment for referral bias on the sensitivity and specificity of single photon emission computed tomography for the diagnosis of coronary artery disease. Am J Med. 2002;112:290–297.
    OpenUrlCrossRefPubMed
  35. 35.↵
    1. Patel MR,
    2. Dai D,
    3. Hernandez AF,
    4. et al
    . Prevalence and predictors of nonobstructive coronary artery disease identified with coronary angiography in contemporary clinical practice. Am Heart J. 2014;167:846–852.e2.
    OpenUrlCrossRefPubMed
  36. 36.↵
    1. Al Moudi M,
    2. Sun Z,
    3. Lenzo N
    . Diagnostic value of SPECT, PET and PET/CT in the diagnosis of coronary artery disease: a systematic review. Biomed Imaging Interv J. 2011;7:e9.
    OpenUrlPubMed
  37. 37.↵
    1. Gould KL
    . Does coronary flow trump coronary anatomy? JACC Cardiovasc Imaging. 2009;2:1009–1023.
    OpenUrlCrossRefPubMed
  38. 38.↵
    1. Parker MW,
    2. Iskandar A,
    3. Limone B,
    4. et al
    . Diagnostic accuracy of cardiac positron emission tomography versus single photon emission computed tomography for coronary artery disease: a bivariate meta-analysis. Circ Cardiovasc Imaging. 2012;5:700–707.
    OpenUrlAbstract/FREE Full Text
  39. 39.↵
    1. Cerqueira MD,
    2. Nguyen P,
    3. Staehr P,
    4. Underwood SR,
    5. Iskandrian AE
    ; ADVANCE-MPI Trial Investigators. Effects of age, gender, obesity, and diabetes on the efficacy and safety of the selective A2A agonist regadenoson versus adenosine in myocardial perfusion imaging integrated ADVANCE-MPI trial results. JACC Cardiovasc Imaging. 2008;1:307–316.
    OpenUrlCrossRefPubMed
  40. 40.↵
    1. Hachamovitch R,
    2. Hayes SW,
    3. Friedman JD,
    4. Cohen I,
    5. Berman DS
    . Comparison of the short-term survival benefit associated with revascularization compared with medical therapy in patients with no prior coronary artery disease undergoing stress myocardial perfusion single photon emission computed tomography. Circulation. 2003;107:2900–2907.
    OpenUrlAbstract/FREE Full Text
  • Received for publication January 2, 2015.
  • Accepted for publication July 16, 2015.
PreviousNext
Back to top

In this issue

Journal of Nuclear Medicine: 56 (12)
Journal of Nuclear Medicine
Vol. 56, Issue 12
December 1, 2015
  • Table of Contents
  • Table of Contents (PDF)
  • About the Cover
  • Index by author
Print
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for your interest in spreading the word on Journal of Nuclear Medicine.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Clinical Utility of Enhanced Relative Activity Recovery on Systolic Myocardial Perfusion SPECT: Lessons from PET
(Your Name) has sent you a message from Journal of Nuclear Medicine
(Your Name) thought you would like to see the Journal of Nuclear Medicine web site.
Citation Tools
Clinical Utility of Enhanced Relative Activity Recovery on Systolic Myocardial Perfusion SPECT: Lessons from PET
Danai Kitkungvan, Pimprapa Vejpongsa, Ketan P. Korrane, Stefano Sdringola, K. Lance Gould
Journal of Nuclear Medicine Dec 2015, 56 (12) 1882-1888; DOI: 10.2967/jnumed.115.153759

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
Clinical Utility of Enhanced Relative Activity Recovery on Systolic Myocardial Perfusion SPECT: Lessons from PET
Danai Kitkungvan, Pimprapa Vejpongsa, Ketan P. Korrane, Stefano Sdringola, K. Lance Gould
Journal of Nuclear Medicine Dec 2015, 56 (12) 1882-1888; DOI: 10.2967/jnumed.115.153759
Twitter logo Facebook logo LinkedIn logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One
Bookmark this article

Jump to section

  • Article
    • Abstract
    • MATERIALS AND METHODS
    • RESULTS
    • DISCUSSION
    • CONCLUSION
    • DISCLOSURE
    • Footnotes
    • REFERENCES
  • Figures & Data
  • Info & Metrics
  • PDF

Related Articles

  • SPECT Myocardial Perfusion Imaging: Poststress, End Systolic Images and the Ongoing Effort to Improve Diagnostic Accuracy
  • This Month in JNM
  • PubMed
  • Google Scholar

Cited By...

  • SPECT Myocardial Perfusion Imaging: Poststress, End Systolic Images and the Ongoing Effort to Improve Diagnostic Accuracy
  • Google Scholar

More in this TOC Section

  • Feasibility of Ultra-Low-Activity 18F-FDG PET/CT Imaging Using a Long–Axial-Field-of-View PET/CT System
  • Cardiac Presynaptic Sympathetic Nervous Function Evaluated by Cardiac PET in Patients with Chronotropic Incompetence Without Heart Failure
  • Validation and Evaluation of a Vendor-Provided Head Motion Correction Algorithm on the uMI Panorama PET/CT System
Show more Clinical Investigations

Similar Articles

Keywords

  • Systolic myocardial perfusion SPECT
  • ECG gated SPECT perfusion images
  • myocardial perfusion imaging
  • SPECT image artifact
SNMMI

© 2025 SNMMI

Powered by HighWire