Zobrazeno 1 - 10
of 483
pro vyhledávání: '"High-output heart failure"'
Autor:
Enklajd Marsela, MD, Eric Hirsch, MD, Leandro Slipczuk, MD, PhD, Mark I. Travin, MD, Renée M. Moadel, MD, MS, Ulrich P. Jorde, MD, Sasa Vukelic, MD, PhD
Publikováno v:
JACC: Case Reports, Vol 29, Iss 14, Pp 102387- (2024)
We introduce the innovative use of technetium-99m–labeled macroaggregated albumin to diagnose high-output heart failure in a patient with multiple myeloma with persistent congestion symptoms. Symptom resolution occurred with lenalidomide and steroi
Externí odkaz:
https://doaj.org/article/10593ebb1b954aa69a6b6a7a6e6fe5ad
Publikováno v:
ESC Heart Failure, Vol 10, Iss 4, Pp 2686-2693 (2023)
Abstract Wet beriberi is a rare but fatal disease in modern society. The nonspecific clinical manifestations, including symptoms of heart failure and recalcitrant lactic acidosis, can prevent timely diagnosis. The use of a pulmonary artery catheter c
Externí odkaz:
https://doaj.org/article/614325ff321241eb8053e47f664da592
Autor:
Paisit Kosum, MD, MSc, Pairoj Chattranukulchai, MD, MSc, Nonthikorn Theerasuwipakorn, MD, MSc, Suchat Sricholwattana, MD, MSc, Aekarach Ariyachaipanich, MD, Monravee Tumkosit, MD, Chaisiri Wanlapakorn, MD, MSc, Suphot Srimahachota, MD, Smonporn Boonyaratavej, MD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 6, Pp 2140-2144 (2023)
A minority of patients with heart failure present in a high-output state. We described an uncommon case of high-output heart failure caused by an iliac arteriovenous fistula (IAVF), a rare but serious complication after lumbar discectomy surgery (LDS
Externí odkaz:
https://doaj.org/article/6fab6ad16f3f414f9bd852490ea73cec
Autor:
Akash Mathavan, Akshay Mathavan, Renuka Reddy, Kirk Jones, Christina Eagan, Hassan Alnuaimat, Ali Ataya
Publikováno v:
Pulmonary Circulation, Vol 13, Iss 4, Pp n/a-n/a (2023)
Abstract Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant hereditary disorder characterized by recurrent spontaneous epistaxis, mucocutaneous telangiectasias, and solid organ arteriovenous malformations (AVMs). Pulmonary hyper
Externí odkaz:
https://doaj.org/article/c3dff2a3748348b2aea223e03cb2e42d
Publikováno v:
Clinical Case Reports, Vol 11, Iss 7, Pp n/a-n/a (2023)
Key Clinical Messages Hereditary hemorrhagic telangiectasia (HHT), a rare hereditary disorder, can cause recurrent massive epistaxis and gastrointestinal bleeding leading to severe anemia. Early diagnosis of HHT is essential to provide timely interve
Externí odkaz:
https://doaj.org/article/cf457e89f7694e9fae67e0267acbacfc
Autor:
Jan Malik, Anna Valerianova, Satu Sinikka Pesickova, Kristyna Michalickova, Zuzana Hladinova, Zdenka Hruskova, Vladimira Bednarova, Katarina Rocinova, Monika Tothova, Marketa Kratochvilova, Lucie Kaiserova, Kristina Buryskova Salajova, Vaclav Lejsek, Martin Sevcik, Vladimir Tesar
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
IntroductionHeart failure (HF) is a serious complication of end-stage kidney disease (ESKD). However, most data come from retrospective studies that included patients on chronic hemodialysis at the time of its initiation. These patients are frequentl
Externí odkaz:
https://doaj.org/article/9cdeba0fcad04194a6995256714d4f14
Publikováno v:
BMC Cardiovascular Disorders, Vol 22, Iss 1, Pp 1-7 (2022)
Abstract Background High-output heart failure is a rare condition that occurs when the heart is unable to respond to a sustained increase in blood demand. On echocardiography, a cardiac index of > 4 L/min/m2 (or 6 L/min) is a clear indicator of this
Externí odkaz:
https://doaj.org/article/57f7e11410ea4931926089e4bac70f1e
Autor:
Yadin Bornstein, MD, M. Libby Weaver, MD, Courtenay M. Holscher, MD, PhD, Thomas Reifsnyder, MD
Publikováno v:
Journal of Vascular Surgery Cases and Innovative Techniques, Vol 7, Iss 3, Pp 529-531 (2021)
High-output heart failure can occur in patients undergoing hemodialysis via permanent access. We have described two cases of hyperacute high-output heart failure. Two patients with multiple previous failed access attempts presented for redo access. E
Externí odkaz:
https://doaj.org/article/6837d2536b1a476bae2667479edd603a
Autor:
Lucas R. Cusumano, Joseph A. Tesoriero, Craig B. Wilsen, James Sayre, Matthew Quirk, Justin P. McWilliams
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-7 (2021)
Abstract Background Hepatic arteriovenous malformations (AVMs) in hereditary hemorrhagic telangiectasia (HHT) patients are most commonly hepatic artery to hepatic venous shunts which can result in high-output heart failure. This condition can be debi
Externí odkaz:
https://doaj.org/article/6b13cdf3a31a413c89e0e44ba34660a7
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