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Reproducibility of CT signs of right heart strain in acute
pulmonary embolism
Poster No.:
B-397
Congress:
ECR 2010
Type:
Scientific Paper
Topic:
Chest
Authors:
J. M. Barraza Jr. , C. Thilo , U. J. Schoepf , J. W. Nance Jr. , J. G.
1
1
1
1
1
2 1
1
2
Ravenel , P. Costello , D. K. Kang ; Charleston, SC/US, Suwon/
KR
Keywords:
Pulmonary embolism, Right heart strain, Computed tomography
angiography
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Page 1 of 18
Purpose
Purpose: To determine the interobserver reproducibility of previously-described CTPA
findings to indicate RV dysfunction, with the goal of identifying the most consistent, least
observer-dependent method.
Introduction:
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Acute pulmonary embolism (PE) is a common but deadly event with a 3
month mortality rate of up to 17.4%.
Even if PE is properly treated with anticoagulation, the mortality rate in
hemodynamically stable patients varies from 8.1% to 15.1%.
The most common cause of death in PE patients is acute right heart failure.
Acute PE increases the pressure of the pulmonary arterial system and right
ventricle (RV), resulting in RV dysfunction, which may progress to right heart
failure and circulatory collapse.
Patients with RV dysfunction have a higher mortality rate than those without,
even if they are initially hemodynamically stable.
The presence of RV dysfunction is a marker for adverse clinical outcome in
patients with acute PE.
Contrast medium enhanced Computed Tomography Pulmonary
Angiography (CTPA) is increasingly used as the first-line imaging test in
suspected PE, and is available 24 hours a day at most institutions.
CTPA not only allows direct visualization of emboli, but also provides
information regarding right-heart status.
The literature shows variable results for the prognostic power of CTPA
evidence of RV dysfunction as a predictor of adverse outcomes.
This variability may, in part, be explained by the somewhat subjective nature
of diagnosing RV dysfunction via CTPA, since formal criteria for establishing
these signs of dysfunction are not available.
Methods and Materials
Patients:
We retrospectively identified 52 consecutive patients hospitalized at our institution
between October 2008 and August 2009 with acute PE diagnosed on CTPA.
Page 2 of 18
Two patients were excluded from the study due to insufficient contrast enhancement of
ventricular chambers for reliable delineation of the endocardial borders; thus a total of 50
patients were eligible for the study.
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The mean age of the subjects was 56 ± 15 years.
Women: 58% (n=29)
Men: 42% (n=21)
All patients included in this study had undergone a clinical assessment by an attending
physician of the probability of pulmonary embolism, using the Wells scoring system.
•
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33 patients with high probability according to Wells score
17 patients with abnormal D-Dimer test.
CTPA Acquisition:
Non-ECG gated CTPA using a 64-slice multi detector-row CT system (Somatom
Sensation, Siemens, Forchheim, Germany)
Image acquisition parameters
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0.33 msec gantry rotation time
32×0.6 mm collimation with z-flying focal spot technique
120 kV, 160 mAseff
Pitch of 1.2
A reconstructed section-thickness of 1 mm
Contrast-medium enhancement
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100 mL of a non-ionic iodinated contrast medium (Ultravist 370, BayerSchering, Berlin, Germany) injected at 4 mL/sec
Automated bolus-triggering with a threshold of 100 HU
CTPA Interpretation (Figure 1 on page 6):
All CTPA studies were independently reviewed by two observers with 6 and 3 years posttraining experience, respectively, in cardiothoracic CT.
Observers were blinded to the patients' clinical characteristics. Studies were reviewed
electronically on a clinical workstation (Multi Modality Workplace, Siemens).
The window and level settings were individually adjusted for each patient-study for
optimized display of pulmonary emboli and the cardiac chambers.
Page 3 of 18
The initial clinical diagnosis of PE was confirmed in the presence of at least one filling
defect in the pulmonary artery tree, including at the subsegmental level.
Deviation of the interventricular septum
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Normal (convex toward the RV)
Flattened septum
Septal bowing (convex toward the LV)
IVC Reflux
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1 = no reflux into IVC
2 = trace of reflux into IVC only
3 = reflux into IVC but not hepatic veins
4 = reflux into IVC with opacification of proximal hepatic veins
5 = reflux into IVC with opacification of hepatic veins to the level of the midportion of the liver
6 = reflux into IVC with opacification of distal hepatic veins.
RVDaxial/LVDaxial Ratio
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The two observers identified the axial sections through the RV and LV that
showed the greatest distance, perpendicular to the long axis of the heart,
between the endocardium and the interventricular septum.
RVDaxial and LVDaxial distance were subsequently measured, and the
RVDaxial /LVDaxial ratio was calculated.
RVD4-CH/LVD4-CH Ratio
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Observers independently reconstructed four-chamber (4-CH) views on the
workstation using the approach illustrated in Figure 2 on page 7.
The two observers then identified the levels of reconstructed 4-CH views
for RV and LV that showed the greatest distance between the ventricular
endocardium and the interventricular septum. RVD4-CH and LVD4-CH were
subsequently calculated.
RVV/LVV Ratio
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The volumetric analysis of both ventricles was performed using the
workstation's volume-analysis application (Volume analysis, software
version VE31A, Siemens).
The endocardial contours were semi-automatically segmented from the
valvular plane down to the apex of both ventricles.
Page 4 of 18
This involved manually outlining the endocardial contours on the transverse sections
comprising the minimal and maximal expanse of the ventricle; these were then
automatically propagated to the neighboring sections.
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The RVV/LVV ratio was subsequently calculated.
The time needed to perform workstation volumetric measurements was
recorded.
Statistical Analysis:
Interobserver reproducibility for determining the grade of IVC reflux and the position of
the interventricular septum
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Unweighted Kappa statistics.
The k value for agreement
Poor: < 0.20
Fair: 0.21 - 0.40
Moderate: 0.41 - 0.60
Good: 0.61 - 0.80
Very Good: 0.81 - 1.00
For continuous variables
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Spearman's rank correlation
Bland-Altman analysis
MedCalc (version 10.4.8, MedCalc Software, Mariakerke, Belgium) was used for all
statistical analyses.
Limitations:
The various signs evaluated in the study were not correlated with outside reference
standards, such as echocardiography.
The prognostic value of the findings were not studied for adverse patient outcomes.
•
This study aimed solely at analyzing the observer-dependence of the CT
signs of RV dysfunction
Page 5 of 18
Participation was limited to two observers; additional observers would have increased
the validity of the findings.
The cohort would be too small to meaningfully contribute to existing data.
Another potential limitation of the study is that image acquisition by CTPA was not ECGgated.
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Non-ECG gated CTPA measurement of ventricular chamber size is
invariably inaccurate, because the images are obtained in different phases
of the cardiac cycle.
Both overestimation and underestimation of the CTPA-derived RVD/LVD
ratio may occur because of motion-artifact and insufficient contrast-medium
attenuation.
However, the use of ECG-gated CTPA protocols over routine non-ECG
gated CTPA has been shown to result in only limited incremental diagnostic
improvement.
Lastly, performance of heart chamber volumetry is somewhat, but not substantially more
time consuming.
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Mean 6 minutes 14 sec for observer 1
Mean 7 minutes 22 sec for observer 2
Images for this section:
Page 6 of 18
Fig. 1: CT signs of RV dysfunction in a 57 year old woman with acute PE. A. 4-CH
view shows septal bowing (arrow), convex toward the LV. B. Grade 5 reflux of contrast
medium into the IVC (short arrow) and proximal hepatic veins (long arrows). C and D.
Measurements of maximal RV (C) and LV (D) diameters on transverse sections show
RVDaxial/LVDaxial ratio of 1.3. E and F. Measurements of maximal RV (E) and LV
(F) diameters on 4-CH views show RVD4-CH/LVD4-CH ratio of 1.4. G and H. Semiautomated volumetry of the RV (pink) and LV (orange) displayed on transverse sections
(G) and as coronal reformat (H) shows RVV/LVV ratio of 2.57.
Page 7 of 18
Fig. 2: Reconstruction of 4-CH views: (A) the vertical long-axis plane is aligned on axial
sections through the center of the mitral valve and the LV apex, (B) the horizontal longaxis plane is aligned on the vertical long-axis plane through the center of the mitral valve
and the LV apex, (C) the short-axis plane is aligned on the vertical and horizontal longaxis planes, perpendicular to both, (D) the 4-CH plane is aligned on the short-axis plane
through the anterior mitral valve papillary muscle and the apex of the RV.
Page 8 of 18
Results
The initial clinical diagnosis of acute PE, which had served as an inclusion criterion, was
confirmed by both observers in all 50 patients.
The most central level of involvement with PE:
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Main pulmonary arteries: 12 patients (24%)
Segmental pulmonary artery: 24 patients (48%)
Subsegmental pulmonary artery: 14 patients (28%)
Within 30 days of follow-up
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Death: one patient
Adverse clinical event: 10 patients
6 requiring endotracheal intubation
5 requiring thrombolysis
One requiring vasopressors
One requiring cardiopulmonary resuscitation
During nine-month follow up
•
Death: 4 patients (8%)
Septal Bowing
Observer 1
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Normal in 48% (n=24)
Flattened in 34% (n=17)
Septal bowing in 18% (n=9)
Observer 2
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Normal in 60% (n=30)
Flattened septum in 32% (n=16)
Septal bowing in 8% (n=4)
Overall interobserver reproducibility for describing the position of the ventricular septum:
Page 9 of 18
•
Fair (k=0.32, 95% CI 0.090 - 0.551)
Reproducibility for differentiating normal versus abnormal (i.e. flattening or bowing)
position of the septum:
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Moderate (k=0.44, 95% CI 0.2204 - 0.685)
IVC Reflux
Observer 1
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Grade 1 in 30% (n=15)
Grade 2 in 30% (n=15)
Grade 3 in 18% (n=9)
Grade 4 in 10% (n=5)
Grade 5 in 4% (n=2)
Grade 6 in 8% (n=4)
Observer 2
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Grade 1 in 22% (n=11)
Grade 2 in 42% (n=21)
Grade 3 in 20% (n=10)
Grade 4 in 8% (n=4)
Grade 5 in 8% (n=4)
No reflux (grade 1) vs. minimal (grade 2-3) vs. substantial (grade 4-6):
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Moderate agreement (k=0.57, 95% CI 0.365 - 0.770)
Substantial (grade 4-6) vs. non-substantial reflux (grade 1-3):
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Good agreement (k=0.68, 95% CI 0.408 - 0.946)
Inter-Observer Correlation of CT Measures of Right Heart Dysfunction
Observer 1
Observer 2
Correlation
coefficient*
RVDaxial
4.5 ± 0.9 cm
4.5 ± 0.7 cm
0.88 (p<0.0001)
LVDaxial
4.1 ± 0.9 cm
4.0 ± 0.8 cm
0.87 (p<0.0001)
RVDaxial/LVDaxial
ratio
1.16 ± 0.45
1.18 ± 0.4
0.88 (p<0.0001)
Page 10 of 18
RVD4-CH
4.4 ± 0.7 cm
4.5 ± 0.6 cm
0.83 (p<0.0001)
LVD4-CH
3.9 ± 0.8 cm
3.9 ± 0.8 cm
0.82 (p<0.0001)
1.21 ± 0.38
0.85 (p<0.0001)
RVD4-CH
ratio
/LVD4-CH 1.21 ± 0.46
RVV
130.5 ± 48.9 ml
130.1 ± 47.9 ml
0.95 (p<0.0001)
LVV
92.6 ± 42.2 ml
90.4 ± 39.9 ml
0.97 (p<0.0001)
RVV/LVV ratio
1.68 ± 1.06
1.71 ± 1.14
0.93 (p<0.0001)
RVDaxial = RV diameter on axial sections, LVDaxial = LV diameter on axial sections
RVD4-CH = RV volume on 4-CH views, LVD4-CH = LV volume on 4-CH views
RVV = RV volume, LVV = LV volume, * Spearman' rank correlation coefficient
RVD/LVD Ratio
On Bland-Altman analysis
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RVDaxial/LVDaxial ratio measurements (Figure 1 on page 12):
The means = 0.014
Standard deviations = 0.195
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RVD4-CH/LVD4-CH ratio (Figure 2 on page 12):
The means = 0.001
Standard deviations = 0.242
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RVV/LVV ratio (Figure 3 on page 13):
The means = 0.033
Standard deviations = 0.229
Page 11 of 18
Images for this section:
Fig. 1: Bland-Altman analysis of RVDaxial/LVDaxial ratio measured by the two observers
Page 12 of 18
Fig. 2: Bland-Altman analysis of RVD4-CH/LVD4-CH ratio measured by the two
observers.
Page 13 of 18
Fig. 3: Bland-Altman analysis of RVV/LVV ratio measured by the two observers
Page 14 of 18
Conclusion
This study shows that considerable differences exist in the interobserver reproducibility
of CT findings of RV dysfunction on CTPA in patients with acute PE.
Cardiac chamber measurements are more reproducible than septal bowing and IVC
reflux, which have more limited interobserver correlation for establishing their presence
and severity.
According to the data, volumetric determination of the RVV/LVV ratio is the least userdependent and most reproducible.
We propose the use of volumetric measurements of cardiac chambers to study RV
dysfunction in patients with acute PE.
References
1. Alpert JS, Smith R, Carlson J, Ockene IS, Dexter L, Dalen JE. Mortality in patients
treated for pulmonary embolism. JAMA 1976;236:1477-1480
2. Carson JL, Kelley MA, Duff A et al. The clinical course of pulmonary embolism. N Engl
J Med 1992;326:1240-1245
3. Van Beek EJ, Kuijer PM, Buller HR, Brandjes DP, Bossuyt PM, ten Cate JW.
The clinical course of patients with suspected pulmonary embolism. Arch Intern Med
1997;157:2593-2598
4. Goldhaber SZ, Visani L, De Rosa M. Acute pulmonary embolism: clinical outcomes
in the International Cooperative Pulmonary Embolism Registry (ICOPER). Lancet
1999;353:1386-1389
5. Kaspar W, Konstantinides S, Geibel A, et al. Management strategies and determinants
of outcome in acute major pulmonary embolism: results of a multicenter registry. J Am
Coll Cardiol 1997;30:1165-1171
6. Ribeiro A, Lindmarker P, Juhlin-Dannfelt A, Johnsson H, Jorfeldt L. Echocardiography
Doppler in pulmonary embolism: right ventricular dysfunction as a predictor of mortality
rate. Am Heart J 1997;134:479-487
Page 15 of 18
7. Grifoni S, Olivotto I, Cecchini P, et al. Short-term clinical outcome of patients with acute
pulmonary embolism, normal blood pressure, and echocardiographic right ventricular
dysfunction. Circulation 2000;101:2817-2822
8. Goldhaber SZ (2002) Echocardiography in the management of pulmonary embolism.
Ann Intern Med 2002;136:691-700
9. Kucher N, Rossi E, De Rosa M, Goldhaber SZ. Prognostic role of echocardiography
among patients with acute pulmonary embolism and a systolic arterial pressure of 90 mm
Hg or higher. Arch Intern Med 2005;165:1777-1781
10. Lomis NN, Yoon HC, Moran AG, Miller FJ. Clinical outcomes of patients after a
negative spiral CT pulmonary arteriogram in the evaluation of acute pulmonary embolism.
J Vasc Interv Radiol 1999;10:707-712
11. Costantino MM, Randall G, Gosselin M, Brandt M, Spinning K, Vegas CD. CT
angiography in the evaluation of acute pulmonary embolus. AJR Am J Roentgenol
2008;191:471-4.
12. Eng J, Krishnan JA, Segal JB, et al. Accuracy of CT in the diagnosis of pulmonary
embolism: a systematic literature review. AJR Am J Roentgenol 2004;183:1819-27.
13. Ginsberg MS, King V, Panicek DM. Comparison of interpretations of CT angiograms
in the evaluation of suspected pulmonary embolism by on-call radiology fellows and
subsequently by radiology faculty. AJR Am J Roentgenol 2004;182:61-6.
14. Schoepf UJ, Goldhaber SZ, Costello P. Spiral computed tomography for acute
pulmonary embolism. Circulation 2004;109:2160-2167
15. Ocak I, Fuhrman C. CT angiography findings of the left atrium and right ventricle in
patients with massive pulmonary embolism. AJR Am J Roentgenol 2008;191:1072-6.
16. Oliver TB, Reid JH, Murchison JT. Interventricular septal shift due to massive
pulmonary embolism shown by CT pulmonary angiography: an old sign revisited. Thorax
1998;53:1092-1094
17. Reid JH, Murchison JT. Acute right ventricular dilatation: a new helical CT sign of
massive pulmonary embolism. Clin Radiol 1998;53:694-698
18. Contractor S, Maldjian PD, Sharma VK, Gor DM. Role of helical CT in detecting
right ventricular dysfunction secondary to acute pulmonary embolism. J Comput Assist
Tomogr 2002;26:587-591
19. Araoz PA, Gotway MB, Trowbridge RL, et al. Helical CT pulmonary angiography
predictors of in-hospital morbidity and mortality in patients with acute pulmonary
embolism. J Thorac Imaging 2003;18:207-216
Page 16 of 18
20. Collomb D, Paramelle PJ, Calaque O, et al. Severity assessment of acute pulmonary
embolism: evaluation using helical CT. Eur Radiol 2003;13:1508-1514
21. Aviram G, Rogowski O, Gotler Y, et al. Real-time risk stratification of patients with
acute pulmonary embolism by grading the reflux of contrast medium into the inferior
vena cava on computerized tomographic pulmonary angiography. J Thromb Haemost
2008;6:1488-1493.
22. Quiroz R, Kucher N, Schoepf UJ, et al. Right ventricular enlargement on chest
computed tomography: prognostic role in acute pulmonary embolism. Circulation
2004;109:2401-2404
23. Schoepf UJ, Kucher N, Kipfmueller F, Quiroz R, Costello P, Goldhaber SZ. Right
ventricular enlargement on chest computed tomography: a predictor of early death in
acute pulmonary embolism. Circulation 2004;110:3276-3280
24. Mansencal N, Joseph T, Vieillard-Baron A, et al. Diagnosis of right ventricular
dysfunction in acute pulmonary embolism using helical computed tomography. Am J
Cardiol 2005;95:1260-1263
25. He H, Stein MW, Zalta B, Haramati LB. Computed tomography evaluation of right
heart dysfunction in patients with acute pulmonary embolism. J Comput Assist Tomogr
2006;30:262-266
26. Van der Meer RW, Pattynama PM, van Strijen MJ, et al. Right ventricular
dysfunction and pulmonary obstruction index at helical CT: prediction of clinical
outcome during 3-month follow-up in patients with acute pulmonary embolism. Radiology
2005;235:798-803
27. Do#an H, Kroft LJ, Huisman MV, van der Geest RJ, de Roos A. Right ventricular
function in patients with acute pulmonary embolism: analysis with electrocardiographysynchronized multi-detector row CT. Radiology 2007;242:78-84
28. van Belle A, Büller HR, Huisman MV, Huisman PM, Kaasjager K, Kamphuisen PW,
Kramer MH, Kruip MJ, Kwakkel-van Erp JM, Leebeek FW, Nijkeuter M, Prins MH, Sohne
M, Tick LW; Christopher Study Investigators. Effectiveness of managing suspected
pulmonary embolism using an algorithm combining clinical probability, D-dimer testing,
and computed tomography. JAMA. 2006;295:172-179
29. Piazza G, Goldhaber SZ. Acute pulmonary embolism: part I: epidemiology and
diagnosis. Circulation. 2006;114:e28-32
30. Wells PS, Anderson DR, Rodger M, Ginsberg JS, Kearon C, Gent M, Turpie AG,
Bormanis J, Weitz J, Chamberlain M, Bowie D, Barnes D, Hirsh J. Derivation of a simple
Page 17 of 18
clinical model to categorize patients probability of pulmonary embolism: increasing the
models utility with the SimpliRED D-dimer. Thromb Haemost. 2000;83:416-420
31. Altman DG. Practical statistics for medical research. London, UK: Chapman and Hall,
1991:404
32. Bland JM, Altman DG. Statistical methods for assessing agreement between two
methods of clinical measurement. Lancet 1986;1:307-310
33. Ghaye B, Ghuysen A, Bruyere PJ, D'Orio V, Dondelinger RF. Can CT pulmonary
angiography allow assessment of severity and prognosis in patients presenting with
pulmonary embolism? What the radiologist needs to know. Radiographics 2006;26:23-39
34. Araoz PA, Gotway MB, Harrington JR, Harmsen WS, Mandrekar JN. Pulmonary
embolism: prognostic CT findings. Radiology 2007;242:889-897
35. Gosselin MV, Rubin GD. Altered intravascular contrast material flow dynamics: clues
for refining thoracic CT diagnosis. AJR Am J Roentgenol 1997;169:1597-1603.
36. Ghuysen A, Ghaye B, Willems V, et al. Computed tomographic pulmonary
angiography and prognostic significance in patients with acute pulmonary embolism.
Thorax 2005;60:956-961
37. Ghaye B, Ghuysen A, Willems V, et al. Severe pulmonary embolism: pulmonary artery
clot load scores and cardiovascular parameters as predictors of mortality. Radiology
2006;239:884-891
38. Lim KE, Chan CY, Chu PH, Hsu YY, Hsu WC. Right ventricular dysfunction secondary
to acute massive pulmonary embolism detected by helical computed tomography
pulmonary angiography. Clin Imaging 2005;29:16-21
39. Lu MT, Cai T, Ersoy H, et al. Comparison of ECG-gated versus non-gated CT
ventricular measurements in thirty patients with acute pulmonary embolism. Int J
Cardiovasc Imaging 2009;25:101-107
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