Pulmonary Hypertension : Radiologist’s Role


Yarol R. C., Barış M. M., Şimşek M. K., Cantürk A.

ECR 2023, Vienna, Avusturya, 1 - 05 Mart 2023, ss.8-13

  • Yayın Türü: Bildiri / Tam Metin Bildiri
  • Doi Numarası: 10.26044/ecr2023/c-18696
  • Basıldığı Şehir: Vienna
  • Basıldığı Ülke: Avusturya
  • Sayfa Sayıları: ss.8-13
  • Dokuz Eylül Üniversitesi Adresli: Evet

Özet

To highlight the new data given in Pulmonary Hypertension (PH) 2022 guideline and assess the differences of radiological approach from the old version.

Methods or Background

Pulmonary hypertension (PH) is a heterogeneous disease driven most often by pathogenic remodeling of distal pulmonary arterioles or a congestive (functional) vasculopathy resulting from pulmonary venous hypertension. (1) The latest 2022 ESC/ERS Guidelines divides PH into 5 categories:1- Pulmonary arterial hypertension2- PH associated with left heart disease3- PH associated with lung diseases and/or hypoxia4- Chronic thrombo-embolic pulmonary hypertension5- Pulmonary hypertension with unclear and/or multifactorial mechanisms.

European Society of Cardiology (ESC) and European Respiratory Society (ERS) has published a new guideline on PHT at August 2022. In this guideline new criterias and approaches were described for radiologic modalities.

Results or Findings

Right heart catheterization is the gold standard for PH diagnosis but radiologic modalities (Ultrasound, CT, MRI, DSA) are complementary tools for both diagnosis and classification.In the new guideline; PA-to-aorta ratio cut-off level changed from 1 to 0.9 on Chest computed tomography (CT) . A combination of three parameters (PA diameter ≥30 mm, RVOT wall thickness ≥6 mm and septal deviation ≥140°) was described and defined as highly predictive of PH (Table. 1). CT is also described as a useful tool for determination of parenchymal lung disease and pulmonary veno-occlusive disease findings. Measurement method of the septal deviation angle is applied as connecting midpoint of interventricular septum to the intersections of RV myocardium and interventricular septum (Fig. 1)(3).Digital subtraction angiography and dual CT are recommended over computed tomography pulmonary angiography for the diagnosis of chronic tromboembolic pulmonary hypertension as opposed to the first version (Fig 2)(4).As a main difference from the previous guideline, Cardiac MRI has been presented. MRI is useful to evaluate atrial and ventricular size, morphology, and function and also primary modality to measure right ventricular ejection fraction , stroke volume index and right ventricular end-systolic volume index (Figure 3).Abdominal ultrasound should be obtained to search for etiologic causes such as liver disease, portal hypertension or portocaval shunt (Abernethy malformation) and to evaluate pulmonary hypertention induced end organ dysfunction (Table 2).

Conclusion

ESC-ERS 2022 guideline adds new approaches and suggestions for diagnosis and screening of PH. Radiologic modalities (USG, MR, CT, DSA) are helpful for detecting underlying condition, classification and screening.