Showing posts with label Adrenaline. Show all posts
Showing posts with label Adrenaline. Show all posts

Saturday, 21 June 2025

Chronic Renal Failure and Bleeding Due to Dieulafoy Lesion: Two Case Reports and Literature Review | Chapter 10 | Medicine and Medical Research: New Perspectives Vol. 4

Dieulafoy’s lesions are rare vascular malformations of the gastrointestinal tract. Dieulafoy’s lesion was first reported by Gallard in 1884 and then described in detail by Georges Dieulafoy in 1898. A Dieulafoy’s lesion is an aberrant vessel that does not reduce in caliber when it extends from the submucosa to the mucosa. Damage to this artery can cause severe and intermittent arterial bleeding from small vascular stumps that are difficult to visualize. Multiple factors have been proposed that increase the risk of upper gastrointestinal bleeding in end-stage renal disease patients including platelet dysfunction due to uremia, high prevalence of arteriovenous malformations, various co-morbidities like cardiovascular disease, diabetes mellitus, liver cirrhosis and old age. Furthermore, these catastrophic bleeding episodes frequently result in hemodynamic instability and the need for transfusion of multiple blood products. Recently, uremic syndrome has been identified as a risk factor for gastric mucosal lesions. We present two clinical cases of acute digestive bleeding due to the Dielafoy lesion with chronic kidney disease as the main cause, where two different therapies were performed endoscopically. Endoscopic therapy is still the first-line diagnostic and/or treatment option for Dieulafoy’s lesion. This study concluded with the results of the patients that the best therapy was the application of the hemostatic hemoclip on the injury vs. the injection with adrenaline on the wound site. Uremia is identified as a risk factor for upper gastrointestinal bleeding in patients with pre-existing Dieulafoy lesions, as well as a higher incidence of new bleeding.

 

Author (s) Details

 

Gustavo Adolfo Hernández Valdez
Department of Internal Medicine, ISSSTE APP General Hospital of Tepic, Tepic, Nayarit, Mexico.

 

Diana Estefanía Ibarra García
Department of Internal Medicine, ISSSTE APP General Hospital of Tepic, Tepic, Nayarit, Mexico.

 

Juan Antonio Contreras Escamilla
Department of Internal Medicine, ISSSTE APP General Hospital of Tepic, Tepic, Nayarit, Mexico.

 

Janette Alejandra Gamiño Gutierrez
Hospital Civil de Guadalajara Fray, Mexico.

 

Francisco Manuel Tonatiuh Carrillo Beltran
Department of Internal Medicine, ISSSTE APP General Hospital of Tepic, Tepic, Nayarit, Mexico.

 

Ulises Solis Gomez
Department of Internal Medicine, ISSSTE APP General Hospital of Tepic, Tepic, Nayarit, Mexico.

Jocelyn Nataly Quintero Meléndez
Department of Internal Medicine, ISSSTE APP General Hospital of Tepic, Tepic, Nayarit, Mexico.

 

Ivan Alejandro Medina Jimenez
Department of Internal Medicine, ISSSTE APP General Hospital of Tepic, Tepic, Nayarit, Mexico.

 

Marco Antonio González Villar
Department of Internal Medicine, ISSSTE APP General Hospital of Tepic, Tepic, Nayarit, Mexico.

 

Jorge Rojas Morales
Department of Internal Medicine, ISSSTE APP General Hospital of Tepic, Tepic, Nayarit, Mexico.

 

 

Please see the book here:- https://doi.org/10.9734/bpi/mmrnp/v4/2410

Thursday, 27 May 2021

Adrenaline Hunters: Past, Present and Future at 1900 | Chapter 17 | Highlights on Medicine and Medical Research Vol. 10

 The Italian anatomist Eustachio characterised the adrenal gland in 1564, but its physiologic function was unknown for three centuries. Nobody knew what Addison's disease was until 1855, when it was first reported. In 1894, Oliver and Schäfer discovered that adrenal extracts can raise blood pressure. As a result, in the late 1890s, a group of highly driven scientists set out to isolate the active principle for medicinal use, but they all failed. For example, Abel's epinephrine preparation was an inactive benzoylated derivative. Takamine, a Japanese industrial chemist, and his young associate Uenaka, who had settled in New York on August 5, 1900, succeeded in crystallising the adrenal extract using a method that was not before used. In the vacuum pan, the active principle was separated, crystallised with ammonia, and validated by the Vulpian reaction. According to ‘Uenaka's Experimental Memorandum,' the unique crystal was given the name ‘adrenalin' (no “e”) on November 7, 1900. Simultaneously, Takamine submitted for a US patent, which was granted on June 2, 1903, and Parke, Davis & Company trademarked the name "Adrenalin" for use in the global market. Adrenaline has saved many lives as a hemostatic during surgery and in the treatment of heart failure. Using the name "adrenaline" has historical, etymological, and practical grounds.

Author(s) Details

Tetsumori Yamashima
Department of Psychiatry and Neurobiology, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.

View Book :- https://stm.bookpi.org/HMMR-V10/article/view/1128