Zobrazeno 1 - 10
of 149
pro vyhledávání: '"High‐output cardiac failure"'
Autor:
Dan‐Ying Lee, Ting Chen, Wei‐Chieh Huang, Ruey‐Hsing Chou, Cheng‐Hsueh Wu, Chih‐Yu Yang, Chiu‐Yang Lee, Chih‐Ching Lin, Der‐Cherng Tarng
Publikováno v:
ESC Heart Failure, Vol 11, Iss 1, Pp 189-197 (2024)
Abstract Aims Patients with high‐flow arteriovenous (AV) access are at risk of developing high‐output cardiac failure (HOCF) and subsequent hospitalization. However, diagnosing HOCF is challenging and often requires invasive procedures. The role
Externí odkaz:
https://doaj.org/article/e19a4b9daa644945873664aa45451c8c
Autor:
Daisuke Takahashi, Kan Katayama, Yoshinobu Iyoda, Ayumi Fukumori, Kayo Tsujimoto, Masahiro Yamawaki, Fumika Tanaka, Ryosuke Saiki, Keiko Oda, Yasuo Suzuki, Tomohiro Murata, Yoshinaga Okugawa, Kaoru Dohi
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Most male X-linked Alport syndrome patients with COL4A5 nonsense mutations experience end-stage kidney failure by 30 years old. Although there is no definition of high-flow arteriovenous fistula, access blood flows greater than 2000 mL/min might pred
Externí odkaz:
https://doaj.org/article/94e7b2ef08554d22a75e841494502b91
Autor:
Ming-zhe Wen, Xin-yu Li, Yu-chen Shen, Zhen-feng Wang, Lian-zhou Zheng, De-ming Wang, Xin-dong Fan, Li-xin Su, Xi-tao Yang
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
PurposeThe aim of this study was to describe the treatment technique, outcomes, and complications of Schobinger stage IV head and neck arteriovenous malformations (HNAVMs) with associated high-output cardiac failure (HOCF) using ethanol and coils wit
Externí odkaz:
https://doaj.org/article/db085a31bb024b90ad9d716fe52af4b9
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)
Abstract Background Systemic bevacizumab is a novel targeted anti-angiogenic therapy for high-output cardiac failure (HOCF) in hereditary hemorrhagic telangiectasia (HHT) but published data is limited. This survey-based study measured physician-repor
Externí odkaz:
https://doaj.org/article/a13e6bcb08d144d589427e5835c793f3
Akademický článek
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Autor:
Agnes S. Kim, Katharine J. Henderson, Sumeet Pawar, Min Jung Kim, Shahnaz Punjani, Jeffrey S. Pollak, John T. Fahey, Guadalupe Garcia‐Tsao, Lissa Sugeng, Lawrence H. Young
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 9, Iss 20 (2020)
Background Patients with hereditary hemorrhagic telangiectasia have liver vascular malformations that can cause high‐output cardiac failure (HOCF). Known sequelae include pulmonary hypertension, tricuspid regurgitation, and atrial fibrillation. Met
Externí odkaz:
https://doaj.org/article/9e117051f89748ec8e33003bb18d3982
Publikováno v:
American Journal of Perinatology Reports, Vol 07, Iss 01, Pp e1-e4 (2017)
Abstract Background Pial arteriovenous fistula (AVF) is composed of one or more direct arterial feeding vessels with a single draining vein without nidus. A patient with the disease with high-flow AV shunting in the neonatal period not only suffers
Externí odkaz:
https://doaj.org/article/e718653a4ffa47868e0b675213b643d1
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Rebeca Gregorio-Hernández, Ester Sanz-López, Alejandra Aguado-Del Hoyo, Gema Manrique-Martín, Juan Carlos De-Agustín, Manuel Sánchez-Luna
Publikováno v:
American Journal of Perinatology Reports, Vol 06, Iss 02, Pp e216-e221 (2016)
Abstract Introduction Congenital umbilical arteriovenous malformations (AVMs) are extremely rare. We present the first case of congenital umbilical AVM with feeding arteries originating not only from abdominal but also from the mammary arteries.
Externí odkaz:
https://doaj.org/article/682dbb9bb48c405c834e3e18a3c550b5
Autor:
Amitava Sur, Heran Manraj, Pascal M. Lavoie, Ken Lim, Douglas Courtemanche, Paul Brooks, Susan Albersheim
Publikováno v:
American Journal of Perinatology Reports, Vol 06, Iss 01, Pp e99-e103 (2016)
Abstract Rapidly involuting congenital hemangiomas (RICH) are the commonest variety of congenital hemangioma, often diagnosed antenatally as high-flow arteriovenous shunts causing hemodynamic compromise to the fetus. The postnatal management of such
Externí odkaz:
https://doaj.org/article/8727ad063db84fd196bfc53cd5ddb67f