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Multimodality imaging of chronic thromboembolic pulmonary hypertension : new insights into old challenges
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<p dir="ltr"><b>BACKGROUND:</b><br><br>Most forms of pulmonary hypertension carry unsatisfactory prognosis with the notable exception of chronic thromboembolic pulmonary hypertension (CTEPH), a complication of acute pulmonary embolism (APE) where complete cure is possible with pulmonary endarterectomy (PEA). CTEPH is often underdiagnosed leading to delayed referral or missed diagnosis. Computed Tomography Pulmonary Angiography (CTPA) is commonly performed in patients with suspected CTEPH or dyspnoea of unknown cause; however, the frequency of misdiagnosis of CTEPH findings on CTPA is currently unknown. There is abundant CT literature describing arterial abnormalities of CTEPH but none regarding venous flow disturbances. Hypodense filling defects within the pulmonary veins (pulmonary vein sign: PVS) has been noted in APE but its presence and relevance in CTEPH is unascertained. CTPA used for CTEPH diagnosis contains information on cardiac chamber size that has potential for adverse outcome prediction but this is unproven. As normative values for atrial volumes on non-ECG gated CTPA is lacking, it is necessary to establish normal ranges prior to appreciating morphological differences in CTEPH. <br><br><b>OBJECTIVES: </b><br><br>Comprehend extent of CTEPH misdiagnosis on CT by radiologists, evaluate venous flow abnormalities in CTEPH with proximal and distal distribution with hemodynamic correlation, derive normal ranges for biatrial volumes on non-ECG gated CT and assess if cardiac chamber size on CTPA is useful for CTEPH risk estimation and outcome prediction. <br><br><b>MATERIALS & METHODS: </b><br><br><b>Study 1:</b> Original CT reports 35 patients awaiting PEA scored for pulmonary vascular, cardiovascular and lung parenchymal abnormalities and compared to reading by two investigators with cardiothoracic subspeciality experience. Control group for expert reads included 35 CTPAs negative for thromboembolism. <b>Study 2:</b> Blinded CTPA analysis of 50 proximal CTEPH cases and 50 controls each in 3 groups— APE, nonthromboembolic cohort, and pulmonary arterial hypertension (PAH). Pulmonary venous flow reduction was assessed by the presence of filling defect of at least 2 cm in a pulmonary vein draining into left atrium.<b> Study 3:</b> Retrospective multi-institutional study of 93 CTEPH cases with CTPA and right heart catheterisation performed with in 3- month period. After excluding 17 suboptimal CTPAs, there were 52 proximal and 24 distal cases. Blood flow in the major pulmonary veins was graded. Subgroup analysis of PVS was performed in 38 proximal cases before and after PEA. <b>Study 4:</b> Of 3334 cases who had CTPA over a 12-month period, 304 also had transthoracic echocardiography (TTE) within a 6-month period. Of these 74 had normal diastology on TTE. After applying CT exclusion criteria (thromboembolic disease, LA attenuation <150 HU, significant motion), planimetry was performed using area length method in 35 patients and compared to TTE. <b>Study 5:</b> Out of 53 patients who had PEA between 2014-2019, 44 had paired CTPA and right heart catheterisation before and after surgery. After excluding 11 cases with suboptimal CTPA, semiautomated and manual CT biatrial and biventricular size quantifications were performed in 33 patients and correlated with hemodynamic parameters. <br><br><b>RESULTS: </b><br><br><b>Study 1:</b> Expert readers correctly identified all 35 CTEPH cases. Amongst original reporters, the terminology “CTEPH” was used in 2 patients. Another 7 descriptive reports picked up combination of PH and few vascular signs of CTEPH without stating a definitive diagnosis. Taking these 9 reports as being consistent with radiologists diagnosing CTEPH, overall sensitivity for original reporters was 26%. Pulmonary arterial abnormalities were described in isolation in 63% with no mention of PH or CTEPH. Signs of PH and mosaic attenuation were documented in 53% and 6% respectively. <b>Study 2:</b> PVS was most prevalent in CTEPH. Compared with all controls, sensitivity and specificity of PVS for CTEPH was 78.0% and 85.3% (95% CI, 64.0–88.5 & 78.6–90.6) versus 34.0% and 70.7% in APE, 8.0% and 62% in nonthromboembolic and 2.0% and 60% in PAH. Occlusive arterial disease was most commonly associated with corresponding absent venous flow. <b>Study 3:</b> There was no significant difference in hemodynamic parameters (mPAP 46±11 and 41±12 mm Hg and PVR 9.4±4.5 and 8.4 ±4.8 WU) between the 2 groups but PVS was more frequent in proximal (79%) than distal (29%) CTEPH. PVS was present in 29/38 patients (76%) before surgery. Postoperatively, 33/38 cases (87%, P<0.001) had normal venous flow. <b>Study 4:</b> Normal ranges for indexed LA and RA volumes were 27 + 5 and 20 + 6 mL/m2, and 30 + 8 and 29 + 9 mL/m2 for TTE and CT respectively. Bland–Altman analysis revealed underestimation of biatrial volumes by TTE. CT intraclass correlation coefficients (ICC 95% CI) for LA and RA volumes were 0.99 (0.96– 1.00) and 0.96 (0.76–0.99), respectively with excellent correlation between semiautomated and manual measurements for left (r 0.99, 95% CI 0.98–0.99) and right atrium (r 0.99, 95% CI 0.99–1.00). <b>Study 5:</b> Indexed right atrioventricular volumes were twice that of left atrioventricular volumes pre-PEA with significant (p < 0.001) augmentation of left heart filling post-PTE. Left to right ventricular ratio cut point ≤0.82 has high sensitivity (91% and 97%) and specificity (88% and 85%) for identifying significant elevations of mean pulmonary artery pressure and pulmonary vascular resistance respectively (AUC 0.90 and 0.95), outperforming atrial ratios (sensitivity 78% and 79%, specificity 82% and 92%, and AUC 0.86 and 0.91). Manual ventricular basal dimension ratio correlates strongly with semiautomated volume ratio (r 0.77, 95% CI 0.64–0.85) and is a quicker alternative with comparable prognostic utility (AUC 0.90 and 0.95). A RV:LV ratio of ≥1.01 can identify significant hemodynamic elevations with the same accuracy as more complex measurements. <br><br><b>CONCLUSION: </b><br><br>Radiologists frequently miss CTEPH findings giving falsely low sensitivity for CT. PVS is easy to detect with higher sensitivity and specificity in CTEPH compared with APE and is not a PAH characteristic. Asymmetric pulmonary venous enhancement is an additional parameter in CT assessment of CTEPH and can differentiate CTEPH from PAH. PVS is a common feature in proximal but infrequent in distal CTEPH. PVS does not correlate with hemodynamic severity. PVS resolution following PEA can be a measure of successful clearance. Cardiac chamber assessment on CTPA is easy and reproducible. A RV:LV ratio of ≥1.01 is a simple metric that can be used for CTEPH outcome prediction.</p><p><br></p><h3>LIST OF SCIENTIFIC PAPERS</h3><p dir="ltr">I. Rogberg AN, <b>Gopalan D</b>, Westerlund E, Lindholm P. Do radiologists detect chronic thromboembolic disease on computed tomography? Acta Radiol. 2019 Nov;60(11):1576-1583. PMID: 30897932.<br><a href="https://doi.org/10.1177/0284185119836232" rel="noreferrer" target="_blank">https://doi.org/10.1177/0284185119836232</a><br><br></p><p dir="ltr">II. <b>Gopalan D</b>, Nordgren-Rogberg A, Le EPV, Pavey H, Tarkin J, Nyrén S, Auger W, Lindholm P. Abnormal Pulmonary Venous Filling: An Adjunct Feature in the Computed Tomography Pulmonary Angiogram Assessment of Chronic Thromboembolic Pulmonary Hypertension. J Am Heart Assoc. 2020 Nov 3;9(21):e018075. PMID: 33115320; PMCID: PMC7763423.<br><a href="https://doi.org/10.1161/JAHA.120.018075" rel="noreferrer" target="_blank">https://doi.org/10.1161/JAHA.120.018075</a><br><br></p><p dir="ltr">III. <b>Gopalan D</b>, Riley JYJ, Leong K, Guo HH, Zamanian RT, Hsi A, Auger W, Lindholm P. Pulmonary Vein Sign on Computed Tomography Pulmonary Angiography in Proximal and Distal Chronic Thromboembolic Pulmonary Hypertension With Hemodynamic Correlation. J Thorac Imaging. 2023 May 1;38(3):159-164. PMID: 36919975; PMCID: PMC10128904.<br><a href="https://doi.org/10.1097/RTI.0000000000000706" rel="noreferrer" target="_blank">https://doi.org/10.1097/RTI.0000000000000706</a><br><br></p><p dir="ltr">IV. <b>Gopalan D</b>, Riley J, Leong K, Alsanjari S, Ariff B, Auger W, Lindholm P. Biatrial Volumetric Assessment by Non-ECG-Gated CT Pulmonary Angiography Correlated with Transthoracic Echocardiography in Patients with Normal Diastology. Tomography. 2022 Nov 17;8(6):2761-2771. PMID: 36412689; PMCID: PMC9680340.<br><a href="https://doi.org/10.3390/tomography8060230" rel="noreferrer" target="_blank">https://doi.org/10.3390/tomography8060230</a><br><br></p><p dir="ltr">V. <b>Gopalan D</b>, Riley JYJ, Leong K, Alsanjari S, Auger W, Lindholm P. Computed Tomography Pulmonary Angiography Prediction of Adverse Long-Term Outcomes in Chronic Thromboembolic Pulmonary Hypertension: Correlation with Hemodynamic Measurements Pre- and Post-Pulmonary Endarterectomy. Tomography. 2023 Sep 26;9(5):1787-1798. PMID: 37888734; PMCID: PMC10611069.<br><a href="https://doi.org/10.3390/tomography9050142" rel="noreferrer" target="_blank">https://doi.org/10.3390/tomography9050142</a></p><p dir="ltr"><br></p>
Title: Multimodality imaging of chronic thromboembolic pulmonary hypertension : new insights into old challenges
Description:
<p dir="ltr"><b>BACKGROUND:</b><br><br>Most forms of pulmonary hypertension carry unsatisfactory prognosis with the notable exception of chronic thromboembolic pulmonary hypertension (CTEPH), a complication of acute pulmonary embolism (APE) where complete cure is possible with pulmonary endarterectomy (PEA).
CTEPH is often underdiagnosed leading to delayed referral or missed diagnosis.
Computed Tomography Pulmonary Angiography (CTPA) is commonly performed in patients with suspected CTEPH or dyspnoea of unknown cause; however, the frequency of misdiagnosis of CTEPH findings on CTPA is currently unknown.
There is abundant CT literature describing arterial abnormalities of CTEPH but none regarding venous flow disturbances.
Hypodense filling defects within the pulmonary veins (pulmonary vein sign: PVS) has been noted in APE but its presence and relevance in CTEPH is unascertained.
CTPA used for CTEPH diagnosis contains information on cardiac chamber size that has potential for adverse outcome prediction but this is unproven.
As normative values for atrial volumes on non-ECG gated CTPA is lacking, it is necessary to establish normal ranges prior to appreciating morphological differences in CTEPH.
<br><br><b>OBJECTIVES: </b><br><br>Comprehend extent of CTEPH misdiagnosis on CT by radiologists, evaluate venous flow abnormalities in CTEPH with proximal and distal distribution with hemodynamic correlation, derive normal ranges for biatrial volumes on non-ECG gated CT and assess if cardiac chamber size on CTPA is useful for CTEPH risk estimation and outcome prediction.
<br><br><b>MATERIALS & METHODS: </b><br><br><b>Study 1:</b> Original CT reports 35 patients awaiting PEA scored for pulmonary vascular, cardiovascular and lung parenchymal abnormalities and compared to reading by two investigators with cardiothoracic subspeciality experience.
Control group for expert reads included 35 CTPAs negative for thromboembolism.
<b>Study 2:</b> Blinded CTPA analysis of 50 proximal CTEPH cases and 50 controls each in 3 groups— APE, nonthromboembolic cohort, and pulmonary arterial hypertension (PAH).
Pulmonary venous flow reduction was assessed by the presence of filling defect of at least 2 cm in a pulmonary vein draining into left atrium.
<b> Study 3:</b> Retrospective multi-institutional study of 93 CTEPH cases with CTPA and right heart catheterisation performed with in 3- month period.
After excluding 17 suboptimal CTPAs, there were 52 proximal and 24 distal cases.
Blood flow in the major pulmonary veins was graded.
Subgroup analysis of PVS was performed in 38 proximal cases before and after PEA.
<b>Study 4:</b> Of 3334 cases who had CTPA over a 12-month period, 304 also had transthoracic echocardiography (TTE) within a 6-month period.
Of these 74 had normal diastology on TTE.
After applying CT exclusion criteria (thromboembolic disease, LA attenuation <150 HU, significant motion), planimetry was performed using area length method in 35 patients and compared to TTE.
<b>Study 5:</b> Out of 53 patients who had PEA between 2014-2019, 44 had paired CTPA and right heart catheterisation before and after surgery.
After excluding 11 cases with suboptimal CTPA, semiautomated and manual CT biatrial and biventricular size quantifications were performed in 33 patients and correlated with hemodynamic parameters.
<br><br><b>RESULTS: </b><br><br><b>Study 1:</b> Expert readers correctly identified all 35 CTEPH cases.
Amongst original reporters, the terminology “CTEPH” was used in 2 patients.
Another 7 descriptive reports picked up combination of PH and few vascular signs of CTEPH without stating a definitive diagnosis.
Taking these 9 reports as being consistent with radiologists diagnosing CTEPH, overall sensitivity for original reporters was 26%.
Pulmonary arterial abnormalities were described in isolation in 63% with no mention of PH or CTEPH.
Signs of PH and mosaic attenuation were documented in 53% and 6% respectively.
<b>Study 2:</b> PVS was most prevalent in CTEPH.
Compared with all controls, sensitivity and specificity of PVS for CTEPH was 78.
0% and 85.
3% (95% CI, 64.
0–88.
5 & 78.
6–90.
6) versus 34.
0% and 70.
7% in APE, 8.
0% and 62% in nonthromboembolic and 2.
0% and 60% in PAH.
Occlusive arterial disease was most commonly associated with corresponding absent venous flow.
<b>Study 3:</b> There was no significant difference in hemodynamic parameters (mPAP 46±11 and 41±12 mm Hg and PVR 9.
4±4.
5 and 8.
4 ±4.
8 WU) between the 2 groups but PVS was more frequent in proximal (79%) than distal (29%) CTEPH.
PVS was present in 29/38 patients (76%) before surgery.
Postoperatively, 33/38 cases (87%, P<0.
001) had normal venous flow.
<b>Study 4:</b> Normal ranges for indexed LA and RA volumes were 27 + 5 and 20 + 6 mL/m2, and 30 + 8 and 29 + 9 mL/m2 for TTE and CT respectively.
Bland–Altman analysis revealed underestimation of biatrial volumes by TTE.
CT intraclass correlation coefficients (ICC 95% CI) for LA and RA volumes were 0.
99 (0.
96– 1.
00) and 0.
96 (0.
76–0.
99), respectively with excellent correlation between semiautomated and manual measurements for left (r 0.
99, 95% CI 0.
98–0.
99) and right atrium (r 0.
99, 95% CI 0.
99–1.
00).
<b>Study 5:</b> Indexed right atrioventricular volumes were twice that of left atrioventricular volumes pre-PEA with significant (p < 0.
001) augmentation of left heart filling post-PTE.
Left to right ventricular ratio cut point ≤0.
82 has high sensitivity (91% and 97%) and specificity (88% and 85%) for identifying significant elevations of mean pulmonary artery pressure and pulmonary vascular resistance respectively (AUC 0.
90 and 0.
95), outperforming atrial ratios (sensitivity 78% and 79%, specificity 82% and 92%, and AUC 0.
86 and 0.
91).
Manual ventricular basal dimension ratio correlates strongly with semiautomated volume ratio (r 0.
77, 95% CI 0.
64–0.
85) and is a quicker alternative with comparable prognostic utility (AUC 0.
90 and 0.
95).
A RV:LV ratio of ≥1.
01 can identify significant hemodynamic elevations with the same accuracy as more complex measurements.
<br><br><b>CONCLUSION: </b><br><br>Radiologists frequently miss CTEPH findings giving falsely low sensitivity for CT.
PVS is easy to detect with higher sensitivity and specificity in CTEPH compared with APE and is not a PAH characteristic.
Asymmetric pulmonary venous enhancement is an additional parameter in CT assessment of CTEPH and can differentiate CTEPH from PAH.
PVS is a common feature in proximal but infrequent in distal CTEPH.
PVS does not correlate with hemodynamic severity.
PVS resolution following PEA can be a measure of successful clearance.
Cardiac chamber assessment on CTPA is easy and reproducible.
A RV:LV ratio of ≥1.
01 is a simple metric that can be used for CTEPH outcome prediction.
</p><p><br></p><h3>LIST OF SCIENTIFIC PAPERS</h3><p dir="ltr">I.
Rogberg AN, <b>Gopalan D</b>, Westerlund E, Lindholm P.
Do radiologists detect chronic thromboembolic disease on computed tomography? Acta Radiol.
2019 Nov;60(11):1576-1583.
PMID: 30897932.
<br><a href="https://doi.
org/10.
1177/0284185119836232" rel="noreferrer" target="_blank">https://doi.
org/10.
1177/0284185119836232</a><br><br></p><p dir="ltr">II.
<b>Gopalan D</b>, Nordgren-Rogberg A, Le EPV, Pavey H, Tarkin J, Nyrén S, Auger W, Lindholm P.
Abnormal Pulmonary Venous Filling: An Adjunct Feature in the Computed Tomography Pulmonary Angiogram Assessment of Chronic Thromboembolic Pulmonary Hypertension.
J Am Heart Assoc.
2020 Nov 3;9(21):e018075.
PMID: 33115320; PMCID: PMC7763423.
<br><a href="https://doi.
org/10.
1161/JAHA.
120.
018075" rel="noreferrer" target="_blank">https://doi.
org/10.
1161/JAHA.
120.
018075</a><br><br></p><p dir="ltr">III.
<b>Gopalan D</b>, Riley JYJ, Leong K, Guo HH, Zamanian RT, Hsi A, Auger W, Lindholm P.
Pulmonary Vein Sign on Computed Tomography Pulmonary Angiography in Proximal and Distal Chronic Thromboembolic Pulmonary Hypertension With Hemodynamic Correlation.
J Thorac Imaging.
2023 May 1;38(3):159-164.
PMID: 36919975; PMCID: PMC10128904.
<br><a href="https://doi.
org/10.
1097/RTI.
0000000000000706" rel="noreferrer" target="_blank">https://doi.
org/10.
1097/RTI.
0000000000000706</a><br><br></p><p dir="ltr">IV.
<b>Gopalan D</b>, Riley J, Leong K, Alsanjari S, Ariff B, Auger W, Lindholm P.
Biatrial Volumetric Assessment by Non-ECG-Gated CT Pulmonary Angiography Correlated with Transthoracic Echocardiography in Patients with Normal Diastology.
Tomography.
2022 Nov 17;8(6):2761-2771.
PMID: 36412689; PMCID: PMC9680340.
<br><a href="https://doi.
org/10.
3390/tomography8060230" rel="noreferrer" target="_blank">https://doi.
org/10.
3390/tomography8060230</a><br><br></p><p dir="ltr">V.
<b>Gopalan D</b>, Riley JYJ, Leong K, Alsanjari S, Auger W, Lindholm P.
Computed Tomography Pulmonary Angiography Prediction of Adverse Long-Term Outcomes in Chronic Thromboembolic Pulmonary Hypertension: Correlation with Hemodynamic Measurements Pre- and Post-Pulmonary Endarterectomy.
Tomography.
2023 Sep 26;9(5):1787-1798.
PMID: 37888734; PMCID: PMC10611069.
<br><a href="https://doi.
org/10.
3390/tomography9050142" rel="noreferrer" target="_blank">https://doi.
org/10.
3390/tomography9050142</a></p><p dir="ltr"><br></p>.
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