Pulmonary Arterial Hypertension PAH is a medical condition serious and severe. In Congo, its epidemiology and its etiologies are poorly understood. This study, aimed at improving the care of patients with PAH, was interested to epidemio-clinical aspects, and prognosis of this entity. This was a retrospective, cross-sectional study carried out from the 1st January 2021 to December 31, 2022 (2 years) in Brazzaville University Hospital. Were included 148 patients, the diagnostic criteria having permit to retain a PAH were compliant to that of the PAPUCO study (PAH if PAPS ≥ 35 mmHg, severe PAH if PAPS ≥ 60 mmHg). The heart failure syndrome was present in 140 cases (94.6%), it was right exclusively in 36 cases (24.3%). The etiologies of the group, they were present in 97 cases (66%) followed group III in 24 cases (16.2%). PAH was said to be severe in 39 cases (26.3%). The evolution has been towards complications in 29 cases (19.6%), lethality in 17 cases (11.5%). Poor prognosis factors were the existence of underlying heart disease underlying (AOR =5.6; p =0.02), male sex (AOR=4.8; p=0.02); hyperkalemia (AOR= 9.4; p=0.00). High blood pressure pulmonary is an increasingly common condition encountered in clinical practice in our context.
Published in | Cardiology and Cardiovascular Research (Volume 8, Issue 1) |
DOI | 10.11648/j.ccr.20240801.11 |
Page(s) | 1-6 |
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This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
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Copyright © The Author(s), 2024. Published by Science Publishing Group |
PAH, Left Heart Disease, Brazzaville, Congo
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APA Style
Ngamami, S. F. M., Taty, R. J., Letomo, K. M. N., Landa, C. M. K., Naibe, G. T., et al. (2024). Pulmonary Arterial Hypertension: Epidemiological, Clinical Aspects and Prognoses in the Cardiology Department and Internal Medicine of CHU Brazzaville. Cardiology and Cardiovascular Research, 8(1), 1-6. https://doi.org/10.11648/j.ccr.20240801.11
ACS Style
Ngamami, S. F. M.; Taty, R. J.; Letomo, K. M. N.; Landa, C. M. K.; Naibe, G. T., et al. Pulmonary Arterial Hypertension: Epidemiological, Clinical Aspects and Prognoses in the Cardiology Department and Internal Medicine of CHU Brazzaville. Cardiol. Cardiovasc. Res. 2024, 8(1), 1-6. doi: 10.11648/j.ccr.20240801.11
AMA Style
Ngamami SFM, Taty RJ, Letomo KMN, Landa CMK, Naibe GT, et al. Pulmonary Arterial Hypertension: Epidemiological, Clinical Aspects and Prognoses in the Cardiology Department and Internal Medicine of CHU Brazzaville. Cardiol Cardiovasc Res. 2024;8(1):1-6. doi: 10.11648/j.ccr.20240801.11
@article{10.11648/j.ccr.20240801.11, author = {Solange Flore Mongo Ngamami and Ruddy Junior Taty and Kivie Mou-moue Ngolo Letomo and Christian Michel Kouala Landa and Gankama Thibault Naibe and Jospin Karel Makani Bassoukouahou and Rog Paterne Bakekolo and Meo Stephane Ikama and Fikahem Ellenga Mbolla}, title = {Pulmonary Arterial Hypertension: Epidemiological, Clinical Aspects and Prognoses in the Cardiology Department and Internal Medicine of CHU Brazzaville}, journal = {Cardiology and Cardiovascular Research}, volume = {8}, number = {1}, pages = {1-6}, doi = {10.11648/j.ccr.20240801.11}, url = {https://doi.org/10.11648/j.ccr.20240801.11}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ccr.20240801.11}, abstract = {Pulmonary Arterial Hypertension PAH is a medical condition serious and severe. In Congo, its epidemiology and its etiologies are poorly understood. This study, aimed at improving the care of patients with PAH, was interested to epidemio-clinical aspects, and prognosis of this entity. This was a retrospective, cross-sectional study carried out from the 1st January 2021 to December 31, 2022 (2 years) in Brazzaville University Hospital. Were included 148 patients, the diagnostic criteria having permit to retain a PAH were compliant to that of the PAPUCO study (PAH if PAPS ≥ 35 mmHg, severe PAH if PAPS ≥ 60 mmHg). The heart failure syndrome was present in 140 cases (94.6%), it was right exclusively in 36 cases (24.3%). The etiologies of the group, they were present in 97 cases (66%) followed group III in 24 cases (16.2%). PAH was said to be severe in 39 cases (26.3%). The evolution has been towards complications in 29 cases (19.6%), lethality in 17 cases (11.5%). Poor prognosis factors were the existence of underlying heart disease underlying (AOR =5.6; p =0.02), male sex (AOR=4.8; p=0.02); hyperkalemia (AOR= 9.4; p=0.00). High blood pressure pulmonary is an increasingly common condition encountered in clinical practice in our context. }, year = {2024} }
TY - JOUR T1 - Pulmonary Arterial Hypertension: Epidemiological, Clinical Aspects and Prognoses in the Cardiology Department and Internal Medicine of CHU Brazzaville AU - Solange Flore Mongo Ngamami AU - Ruddy Junior Taty AU - Kivie Mou-moue Ngolo Letomo AU - Christian Michel Kouala Landa AU - Gankama Thibault Naibe AU - Jospin Karel Makani Bassoukouahou AU - Rog Paterne Bakekolo AU - Meo Stephane Ikama AU - Fikahem Ellenga Mbolla Y1 - 2024/01/18 PY - 2024 N1 - https://doi.org/10.11648/j.ccr.20240801.11 DO - 10.11648/j.ccr.20240801.11 T2 - Cardiology and Cardiovascular Research JF - Cardiology and Cardiovascular Research JO - Cardiology and Cardiovascular Research SP - 1 EP - 6 PB - Science Publishing Group SN - 2578-8914 UR - https://doi.org/10.11648/j.ccr.20240801.11 AB - Pulmonary Arterial Hypertension PAH is a medical condition serious and severe. In Congo, its epidemiology and its etiologies are poorly understood. This study, aimed at improving the care of patients with PAH, was interested to epidemio-clinical aspects, and prognosis of this entity. This was a retrospective, cross-sectional study carried out from the 1st January 2021 to December 31, 2022 (2 years) in Brazzaville University Hospital. Were included 148 patients, the diagnostic criteria having permit to retain a PAH were compliant to that of the PAPUCO study (PAH if PAPS ≥ 35 mmHg, severe PAH if PAPS ≥ 60 mmHg). The heart failure syndrome was present in 140 cases (94.6%), it was right exclusively in 36 cases (24.3%). The etiologies of the group, they were present in 97 cases (66%) followed group III in 24 cases (16.2%). PAH was said to be severe in 39 cases (26.3%). The evolution has been towards complications in 29 cases (19.6%), lethality in 17 cases (11.5%). Poor prognosis factors were the existence of underlying heart disease underlying (AOR =5.6; p =0.02), male sex (AOR=4.8; p=0.02); hyperkalemia (AOR= 9.4; p=0.00). High blood pressure pulmonary is an increasingly common condition encountered in clinical practice in our context. VL - 8 IS - 1 ER -