Zobrazeno 1 - 10
of 1 540
pro vyhledávání: '"Vaso-occlusive Crisis"'
Autor:
Ernesto Calderon Martinez, Stephin Zachariah Saji, Thomas Campos Carmona, Vaidarshi Abbagoni, Mohammad Salman, Mishell Estefanía Llerena Vargas, Suchita Mylavarapu, Druvini Fernando, Lakshmi Sheethal Arvapalli, Nathalia Schettino Samad, Nithin Karnan, Camila Sanchez Cruz
Publikováno v:
eJHaem, Vol 5, Iss 6, Pp 1312-1321 (2024)
Abstract Introduction Sickle cell disease (SCD) is characterized by acute episodes called vaso‐occlusive crises (VOC). VOC is marked by severe pain due to blocked blood vessels by sickled cells. Ketamine has been reported to be effective and safe i
Externí odkaz:
https://doaj.org/article/6cf3fca7e4c84f5887dd9938f99fa3bb
Autor:
Pooja Zanzari, Ashwin Vasava, Jitendra Patel, Kamal Arvindbhai Patel, Pooja Modi, Mitul Navadiya, Kruti Jayant Nathani
Publikováno v:
Global Journal of Transfusion Medicine, Vol 9, Iss 1, Pp 22-27 (2024)
Introduction: Sickle cell disease (SCD) is an inherited single-gene autosomal recessive disorder. Red cell exchange (RCE) refers to the removal of diseased red blood cells (RBCs) in exchange for healthy donor RBCs. In the present study, RCE was perfo
Externí odkaz:
https://doaj.org/article/88c9a65711214b429d2e9d4eafc388f0
Publikováno v:
BMC Research Notes, Vol 17, Iss 1, Pp 1-4 (2024)
Abstract Objectives Hypoxia is a known feature of sickle cell anaemia (SCA) which results from chronic anaemia and recurrent vaso-occlusive crisis (VOC) which can cause tissue ischaemia that leads to an end organ damage. The hallmark of SCA is chroni
Externí odkaz:
https://doaj.org/article/c444992684c744bd8548d67df7e40a25
Publikováno v:
Journal of Vascular Diseases, Vol 3, Iss 1, Pp 77-87 (2024)
Sickle cell disease (SCD) imposes a significant health burden, particularly in low- and middle-income countries where healthcare professionals and resources are scarce. This opinion paper delves into the management strategies employed for vaso-occlus
Externí odkaz:
https://doaj.org/article/22eb414561f346dea68184923ed1d34a
Publikováno v:
The Lancet Regional Health. Europe, Vol 40, Iss , Pp 100901- (2024)
Summary: Background: Historically, sickle cell disease (SCD) patients experiencing frequent hospitalized vaso-occlusive crises (HVOC) have been associated with increased mortality, yet recent data reflecting the widespread use of hydroxyurea and adva
Externí odkaz:
https://doaj.org/article/e9ceec406ba542b8907354716abcda45
Publikováno v:
Jurnal Penyakit Dalam Indonesia, Vol 10, Iss 4, Pp 223-227 (2023)
Sickle cell disease (SCD) is a hemoglobinopathy inherited in an autosomal recessive pattern arising from a mutation causing substitution of valine for glutamic acid in the sixth amino acid of the β-globin chain. The clinical manifestation of SCD var
Externí odkaz:
https://doaj.org/article/9d5bcc3c92504e74847d3428735ccbe6
Publikováno v:
eJHaem, Vol 4, Iss 4, Pp 970-976 (2023)
Abstract Acute chest syndrome (ACS) is a frequent complication of sickle cell disease (SCD). Because coronavirus disease 2019 (COVID‐19) increases mortality and morbidity in many diseases, we retrospectively analyzed the impact of SARS‐CoV‐2 in
Externí odkaz:
https://doaj.org/article/cf051054693f451eb989c0ecaf57d2ce
Publikováno v:
Children, Vol 11, Iss 9, p 1106 (2024)
Sickle cell disease (SCD) is the most common hemoglobinopathy in the world. Sickle cell vaso-occlusive episodes (VOEs) are very painful acute events and the most common complication as well as reason for hospitalization. SCD pain is best evaluated ho
Externí odkaz:
https://doaj.org/article/44410ce2d54145c2bc8bf4305335cdfd
Publikováno v:
Asian Journal of Medical Sciences, Vol 14, Iss 10, Pp 221-226 (2023)
Background: Sickle cell disease (SCD) has various complications among which one of the main organs to be affected is the hepatobiliary system ranging from mild liver function test derangements to significant hepatic abnormalities with marked hyperbil
Externí odkaz:
https://doaj.org/article/cef8543e5e4544ec877646827c65c223
Autor:
Kwaku Marfo, Yvonne Dei-Adomakoh, Catherine Segbefia, Duah Dwomoh, Adeline Edgal, Nancy Ampah, Badarinath Chickballapur Ramachandrachar, Kumaresan Subramanyam, Ashok Natarajan, Olufolake Egbujo, Kenneth I. Ataga
Publikováno v:
BMC Health Services Research, Vol 23, Iss 1, Pp 1-14 (2023)
Abstract Background Sickle cell disease (SCD) is a major public health concern in sub-Saharan Africa, accounting for nearly 75% of the global disease burden. The current analysis evaluated patient characteristics, treatment patterns, healthcare resou
Externí odkaz:
https://doaj.org/article/e6c59267870f4939bf453c91a2c5a4c2