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Navigating pulmonary hypertension: Echocardiography insight into right ventricular function and dynamics

Heart Science Journal · Vol. 6 No. 4 (2025)

DOI
10.21776/ub.hsj.2025.006.04.4
ISSN
2721-9984, 2721-9976
Terbit
2025-10-31
Penerbit
Universitas Brawijaya
Bahasa
en
Lisensi
creativecommons.org/licenses/by/4.0

Abstrak

Pulmonary hypertension (PH) is a pathophysiological disorder characterized by pulmonary vascular remodeling and dysfunction, which may arise in various clinical contexts, particularly in association with cardiovascular and respiratory diseases. PH is characterized by a mean pulmonary arterial pressure (mPAP) exceeding 20 mmHg at rest as determined by hemodynamic assessment via right heart catheterization (RHC), which remains the gold standard for diagnosis. Transthoracic echocardiography (TTE) is recommended as a non-invasive screening tool for the initial evaluation of individuals presenting with symptoms, risk factors, or clinical suspicion of PH. Echocardiography enables the identification of pulmonary hypertension by assessing right ventricular (RV) dysfunction and increased RV pressure overload. A comprehensive assessment of the RV’s dimensions and function is essential in all individuals with PH, given that mortality in PH is correlated with the severity of RV dysfunction. While RHC remains the definitive diagnostic modality for PH, echocardiography provides a valuable, widely available, and non-invasive alternative for estimating pulmonary artery pressures, assessing RV function, and stratifying disease severity, in alignment with current guidelines from the European Society of Cardiology (ESC) and the European Respiratory Society (ERS).

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28 penulis · 112 tautan kepenulisan bersama · 6 lintas organisasi

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  • University of Brawijaya
  • RSUD Prof. Dr. Saiful Anwar Malang
  • Afiliasi tidak diketahui
  • Organisasi berbeda
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Rekan penulisOrganisasiArtikel bersama
Anna Fuji RahimahUniversity of Brawijaya4
Wella KarolinaUniversity of Brawijaya4
Heny MartiniUniversity of Brawijaya4
Setyasih AnjarwaniUniversity of Brawijaya4
Indra PrasetyaUniversity of Brawijaya3
Cholid Tri TjahjonoUniversity of Brawijaya3
Mohammad Saifur RohmanUniversity of Brawijaya2
Ardian RizalUniversity of Brawijaya2
Stefani HarumsariAfiliasi tidak diketahui1
Nugrahanti PrasetyoriniAfiliasi tidak diketahui1
Pande Made DwijayasaAfiliasi tidak diketahui1
Bambang RahardjoUniversity of Brawijaya1
Budi SatrijoUniversity of Brawijaya1
Dea Arie KurniawanUniversity of Brawijaya1
Nikhen NoverikeUniversity of Brawijaya1
Akhmad Isna NurudinullohUniversity of Brawijaya1
Vemmy Lian SaputriUniversity of Brawijaya1
Muhammad FirdausUniversity of Brawijaya1
Indra Jabbar AzizUniversity of Brawijaya1
Danti Utami SetyowatiRSUD Prof. Dr. Saiful Anwar Malang1
Akita Rukmana AkbarUniversity of Brawijaya1
Anastasia ChristineAfiliasi tidak diketahui1
Yosafat Hasiholan Marthin GultomUniversity of Brawijaya1
Daniel Erikson TambunanUniversity of Brawijaya1
Muhammad Azhar RosyidiUniversity of Brawijaya1
Muhammad Reva AdityaUniversity of Brawijaya1

Afiliasi berasal dari OpenAlex; metadata OAI-PMH jurnal tidak memuatnya. Penulis tanpa ID OpenAlex dicocokkan berdasarkan nama, sehingga dua orang bisa tergabung atau satu orang bisa terpisah.

Sumber metadata: OAI-PMH (metadata jurnal) https://heartscience.ub.ac.id/index.php/heartscience/oai, pertama di-harvest 8 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (oai_dc)
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	<dc:title xml:lang="en">Navigating pulmonary hypertension: Echocardiography insight into right ventricular function and dynamics</dc:title>
	<dc:creator xml:lang="en">Rahmawati, Novi</dc:creator>
	<dc:creator xml:lang="en">Yogibuana, Valerinna</dc:creator>
	<dc:subject xml:lang="en">Right Ventricle</dc:subject>
	<dc:subject xml:lang="en">Echocardiography</dc:subject>
	<dc:subject xml:lang="en">Pulmonary Hypertension</dc:subject>
	<dc:description xml:lang="en">Pulmonary hypertension (PH) is a pathophysiological disorder characterized by pulmonary vascular remodeling and dysfunction, which may arise in various clinical contexts, particularly in association with cardiovascular and respiratory diseases. PH is characterized by a mean pulmonary arterial pressure (mPAP) exceeding 20 mmHg at rest as determined by hemodynamic assessment via right heart catheterization (RHC), which remains the gold standard for diagnosis. Transthoracic echocardiography (TTE) is recommended as a non-invasive screening tool for the initial evaluation of individuals presenting with symptoms, risk factors, or clinical suspicion of PH. Echocardiography enables the identification of pulmonary hypertension by assessing right ventricular (RV) dysfunction and increased RV pressure overload. A comprehensive assessment of the RV’s dimensions and function is essential in all individuals with PH, given that mortality in PH is correlated with the severity of RV dysfunction. While RHC remains the definitive diagnostic modality for PH, echocardiography provides a valuable, widely available, and non-invasive alternative for estimating pulmonary artery pressures, assessing RV function, and stratifying disease severity, in alignment with current guidelines from the European Society of Cardiology (ESC) and the European Respiratory Society (ERS).</dc:description>
	<dc:publisher xml:lang="en">Universitas Brawijaya</dc:publisher>
	<dc:date>2025-10-31</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://heartscience.ub.ac.id/index.php/heartscience/article/view/20140</dc:identifier>
	<dc:identifier>10.21776/ub.hsj.2025.006.04.4</dc:identifier>
	<dc:source xml:lang="en">Heart Science Journal; Vol. 6 No. 4 (2025): The Pursuit of Precision: Navigating Risks, Refining Diagnosis, and Securing Long-Term Vascular Outcomes in Contemporary Cardiovascular Practice</dc:source>
	<dc:source>2721-9984</dc:source>
	<dc:source>2721-9976</dc:source>
	<dc:source>10.21776/ub.hsj.2025.006.04</dc:source>
	<dc:language>en</dc:language>
	<dc:relation>https://heartscience.ub.ac.id/index.php/heartscience/article/view/20140/534</dc:relation>
	<dc:rights xml:lang="en">Copyright (c) 2025 Novi Rahmawati, Valerinna Yogibuana</dc:rights>
	<dc:rights xml:lang="en">http://creativecommons.org/licenses/by/4.0</dc:rights>
</oai_dc:dc>