Risk Factors and Natural History of Parastomal Hernia Following Radical Cystectomy and Ileal Conduit

2021 ◽  
Author(s):  
Alireza Ghoreifi ◽  
Evan Allgood ◽  
Gilbert Whang ◽  
Antoin Douglawi ◽  
Wenhao Yu ◽  
...  
2014 ◽  
Vol 191 (5) ◽  
pp. 1313-1318 ◽  
Author(s):  
Nick W. Liu ◽  
Jeromy T. Hackney ◽  
Paul T. Gellhaus ◽  
M. Francesca Monn ◽  
Timothy A. Masterson ◽  
...  

2021 ◽  
Vol 10 (3) ◽  
pp. 1389-1398
Author(s):  
Dechao Feng ◽  
Zhenghao Wang ◽  
Yubo Yang ◽  
Dengxiong Li ◽  
Wuran Wei ◽  
...  

2018 ◽  
Vol 199 (3) ◽  
pp. 766-773 ◽  
Author(s):  
Ahmed A. Hussein ◽  
Youssef E. Ahmed ◽  
Paul May ◽  
Taimoor Ali ◽  
Basim Ahmad ◽  
...  

2006 ◽  
Vol 175 (4S) ◽  
pp. 397-397 ◽  
Author(s):  
Wassim Kassouf ◽  
Philippe E. Spiess ◽  
Gordon A. Brown ◽  
Mark F. Munsell ◽  
H. Barton Grossman ◽  
...  

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Alcivan Batista de Morais Filho ◽  
Thiago Luis de Holanda Rego ◽  
Letícia de Lima Mendonça ◽  
Sulyanne Saraiva de Almeida ◽  
Mariana Lima da Nóbrega ◽  
...  

Abstract Hemorrhagic stroke (HS) is a major cause of death and disability worldwide, despite being less common, it presents more aggressively and leads to more severe sequelae than ischemic stroke. There are two types of HS: Intracerebral Hemorrhage (ICH) and Subarachnoid Hemorrhage (SAH), differing not only in the site of bleeding, but also in the mechanisms responsible for acute and subacute symptoms. This is a systematic review of databases in search of works of the last five years relating to the comprehension of both kinds of HS. Sixty two articles composed the direct findings of the recent literature and were further characterized to construct the pathophysiology in the order of events. The road to the understanding of the spontaneous HS pathophysiology is far from complete. Our findings show specific and individual results relating to the natural history of the disease of ICH and SAH, presenting common and different risk factors, distinct and similar clinical manifestations at onset or later days to weeks, and possible complications for both.


2013 ◽  
Vol 189 (4S) ◽  
Author(s):  
Timothy F. Donahue ◽  
Hebert A. Vargas ◽  
John P. Sfakianos ◽  
Matthew Kent ◽  
William M. Hilton ◽  
...  

PEDIATRICS ◽  
1989 ◽  
Vol 84 (3) ◽  
pp. 500-508 ◽  
Author(s):  
Sanford L. Leikin ◽  
Dianne Gallagher ◽  
Thomas R. Kinney ◽  
Desirée Sloane ◽  
Panpit Klug ◽  
...  

A study of the natural history of sickle hemoglobinopathies was begun in March 1979. By August 1987, a total of 2824 patients <20 years of age were enrolled. There have been 14 670 person-years of followup. Seventy-three deaths have occurred. Most of the deaths were in patients with hemoglobin SS. The peak incidence of death was between 1 and 3 years of age, and the major cause in these young patients was infection. Cerebrovascular accidents and traumatic events exceeded infections as a cause of death in patients > 10 years of age. There was limited success in identifying risk factors for death. Comparison of this study's overall mortality of 2.6% (0.5 deaths per 100 person-years) with previous reports indicates improvement of survival in US patients <20 years of age with sickle hemoglobinopathies. This improvement is most likely due to parental education and counseling about the illness and the early institution of antibotics in suspected infections.


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