Background <p>Branch pulmonary artery (PA) stenosis is a significant congenital heart defect causing elevated pulmonary blood pressure, trans-stenotic pressure drop, and abnormal differential blood flow to the lungs. We propose combined pressure-flow diagnostic parameters, <i>pressure drop coefficient</i> (<i>CDP</i>) and <i>normalized energy loss</i> (<i>Ē</i><sub><i>loss</i></sub>) for improved delineation of stenosis severity. In extension to our previous benchtop experimental study, we performed <i>in vitro</i> experiments using phase contrast magnetic resonance imaging (PC MRI) to evaluate the diagnostic parameters and stenosis severity non-invasively.</p> Methods <p>Subject-specific branch PA test sections representing the main, left, and right PAs (MPA, LPA, and RPA) with a discrete LPA stenosis were manufactured from medical images using additive manufacturing. Three clinically-relevant stenosis severities, 70% area stenosis (AS), 80% AS, and 90% AS, were evaluated at 2 LPM cardiac output under pathophysiologic hemodynamics generated using a mock circulatory loop. 2D (all severities) and 3D (only 70% AS) PC MRI scans were performed to compute the velocity (or flow) and derived pressure drop across the PA test section. The CDP<sub>LPA</sub> and <InlineEquation ID="IEq1"> <EquationSource Format="TEX">\({\overline{E} }_{loss, LPA}\)</EquationSource> <EquationSource Format="MATHML"><math> <msub> <mover> <mi>E</mi> <mo>¯</mo> </mover> <mrow> <mi>l</mi> <mi>o</mi> <mi>s</mi> <mi>s</mi> <mo>,</mo> <mi>L</mi> <mi>P</mi> <mi>A</mi> </mrow> </msub> </math></EquationSource> </InlineEquation> were evaluated for the three stenosis severities using MRI measurements and compared against results from the benchtop study.</p> Results <p>The CDP<sub>LPA</sub> increased with an increase in LPA stenosis severity [70% AS: 11 (2D PC), 11.5 (3D PC); 80% AS: 34.6; 90% AS: 154.2]. These values resulted in an absolute difference of within 107 (2D PC) and 3 (3D PC) compared to the benchtop values. Interestingly, the CDP<sub>LPA</sub> computed by all three methods (benchtop, 2D and 3D PC MRI) showed distinct and non-overlapping ranges for each stenosis severity [70% AS: 11.0–14.5; 80% AS: 34.6–60.7; and 90% AS: 154.2–261.6]. The <InlineEquation ID="IEq2"> <EquationSource Format="TEX">\({\overline{E} }_{loss, LPA}\)</EquationSource> <EquationSource Format="MATHML"><math> <msub> <mover> <mi>E</mi> <mo>¯</mo> </mover> <mrow> <mi>l</mi> <mi>o</mi> <mi>s</mi> <mi>s</mi> <mo>,</mo> <mi>L</mi> <mi>P</mi> <mi>A</mi> </mrow> </msub> </math></EquationSource> </InlineEquation> (absolute) generally increased with an increase in LPA stenosis severity, except for 90% [70% AS: − 435&#xa0;mJ per Q<sub>LPA</sub> (2D PC), − 376&#xa0;mJ per Q<sub>LPA</sub> (3D PC); 80% AS: − 945&#xa0;mJ per Q<sub>LPA</sub>; 90% AS: − 933&#xa0;mJ per Q<sub>LPA</sub> (Q<sub>LPA</sub>–LPA flow rate)].</p> Conclusions <p>The CDP<sub>LPA</sub> demonstrates an improved diagnostic capability over <InlineEquation ID="IEq3"> <EquationSource Format="TEX">\({\overline{E} }_{loss, LPA}\)</EquationSource> <EquationSource Format="MATHML"><math> <msub> <mover> <mi>E</mi> <mo>¯</mo> </mover> <mrow> <mi>l</mi> <mi>o</mi> <mi>s</mi> <mi>s</mi> <mo>,</mo> <mi>L</mi> <mi>P</mi> <mi>A</mi> </mrow> </msub> </math></EquationSource> </InlineEquation> in accurately delineating unilateral PA stenosis severity. Further, PC MRI is a comprehensive and safe clinical modality for the non-invasive diagnosis of branch PA stenosis.</p>

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Non-Invasive Evaluation of Pulmonary Artery Stenosis in Congenital Heart Disease Patients Using Phase Contrast MRI

  • Rupak K. Banerjee,
  • Gavin A. D’Souza,
  • Shreyash M. Manegaonkar,
  • Israel O. Ajiboye,
  • Michael D. Taylor

摘要

Background

Branch pulmonary artery (PA) stenosis is a significant congenital heart defect causing elevated pulmonary blood pressure, trans-stenotic pressure drop, and abnormal differential blood flow to the lungs. We propose combined pressure-flow diagnostic parameters, pressure drop coefficient (CDP) and normalized energy loss (Ēloss) for improved delineation of stenosis severity. In extension to our previous benchtop experimental study, we performed in vitro experiments using phase contrast magnetic resonance imaging (PC MRI) to evaluate the diagnostic parameters and stenosis severity non-invasively.

Methods

Subject-specific branch PA test sections representing the main, left, and right PAs (MPA, LPA, and RPA) with a discrete LPA stenosis were manufactured from medical images using additive manufacturing. Three clinically-relevant stenosis severities, 70% area stenosis (AS), 80% AS, and 90% AS, were evaluated at 2 LPM cardiac output under pathophysiologic hemodynamics generated using a mock circulatory loop. 2D (all severities) and 3D (only 70% AS) PC MRI scans were performed to compute the velocity (or flow) and derived pressure drop across the PA test section. The CDPLPA and \({\overline{E} }_{loss, LPA}\) E ¯ l o s s , L P A were evaluated for the three stenosis severities using MRI measurements and compared against results from the benchtop study.

Results

The CDPLPA increased with an increase in LPA stenosis severity [70% AS: 11 (2D PC), 11.5 (3D PC); 80% AS: 34.6; 90% AS: 154.2]. These values resulted in an absolute difference of within 107 (2D PC) and 3 (3D PC) compared to the benchtop values. Interestingly, the CDPLPA computed by all three methods (benchtop, 2D and 3D PC MRI) showed distinct and non-overlapping ranges for each stenosis severity [70% AS: 11.0–14.5; 80% AS: 34.6–60.7; and 90% AS: 154.2–261.6]. The \({\overline{E} }_{loss, LPA}\) E ¯ l o s s , L P A (absolute) generally increased with an increase in LPA stenosis severity, except for 90% [70% AS: − 435 mJ per QLPA (2D PC), − 376 mJ per QLPA (3D PC); 80% AS: − 945 mJ per QLPA; 90% AS: − 933 mJ per QLPA (QLPA–LPA flow rate)].

Conclusions

The CDPLPA demonstrates an improved diagnostic capability over \({\overline{E} }_{loss, LPA}\) E ¯ l o s s , L P A in accurately delineating unilateral PA stenosis severity. Further, PC MRI is a comprehensive and safe clinical modality for the non-invasive diagnosis of branch PA stenosis.