collection
https://read.qxmd.com/read/27940460/minimal-change-disease
#1
REVIEW
Marina Vivarelli, Laura Massella, Barbara Ruggiero, Francesco Emma
Minimal change disease (MCD) is a major cause of idiopathic nephrotic syndrome (NS), characterized by intense proteinuria leading to edema and intravascular volume depletion. In adults, it accounts for approximately 15% of patients with idiopathic NS, reaching a much higher percentage at younger ages, up to 70%-90% in children >1 year of age. In the pediatric setting, a renal biopsy is usually not performed if presentation is typical and the patient responds to therapy with oral prednisone at conventional doses...
February 7, 2017: Clinical Journal of the American Society of Nephrology: CJASN
https://read.qxmd.com/read/31444174/secular-trends-in-incidence-modality-and-mortality-with-dialysis-receiving-aki-in-children-in-ontario-a-population-based-cohort-study
#2
JOURNAL ARTICLE
Rahul Chanchlani, Danielle Marie Nash, Eric McArthur, Michael Zappitelli, Victoria Archer, John Paul Kuwornu, Amit X Garg, Jason H Greenberg, Stuart L Goldstein, Lehana Thabane, Ron Wald
BACKGROUND AND OBJECTIVES: There is a limited appreciation of the epidemiology of dialysis-receiving AKI in children. The primary objective of the study was to evaluate changes in the incidence of dialysis-receiving AKI among children over a period of 20 years in Ontario, Canada. The secondary objectives were to assess temporal trends in the utilization of various dialysis modalities and 30-day mortality among children with dialysis-receiving AKI. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: All children (29 days to 18 years) who received their first dialysis for AKI between 1996 and 2015 were identified from healthcare administrative databases...
September 6, 2019: Clinical Journal of the American Society of Nephrology: CJASN
https://read.qxmd.com/read/27034399/hla-dq-mismatches-and-rejection-in-kidney-transplant-recipients
#3
JOURNAL ARTICLE
Wai H Lim, Jeremy R Chapman, Patrick T Coates, Joshua R Lewis, Graeme R Russ, Narelle Watson, Rhonda Holdsworth, Germaine Wong
BACKGROUND AND OBJECTIVES: The current allocation algorithm for deceased donor kidney transplantation takes into consideration HLA mismatches at the ABDR loci but not HLA mismatches at other loci, including HLA-DQ. However, the independent effects of incompatibilities for the closely linked HLA-DQ antigens in the context of HLA-DR antigen matched and mismatched allografts are uncertain. We aimed to determine the effect of HLA-DQ mismatches on renal allograft outcomes. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Using data from the Australia and New Zealand Dialysis and Transplant Registry, we examined the association between HLA-DQ mismatches and acute rejections in primary live and deceased donor kidney transplant recipients between 2004 and 2012 using adjusted Cox regression models...
May 6, 2016: Clinical Journal of the American Society of Nephrology: CJASN
https://read.qxmd.com/read/27012951/emergency-department-visits-after-kidney-transplantation
#4
JOURNAL ARTICLE
Jesse D Schold, Nissreen Elfadawy, Laura D Buccini, David A Goldfarb, Stuart M Flechner, Michael P Phelan, Emilio D Poggio
BACKGROUND AND OBJECTIVES: In 2011, there were approximately 131 million visits to an emergency department in the United States. Emergency department visits have increased over time, far outpacing growth of the general population. There is a paucity of data evaluating emergency department visits among kidney transplant recipients. We sought to evaluate the incidence and risk factors for emergency department visits after initial hospital discharge after transplantation in the United States...
April 7, 2016: Clinical Journal of the American Society of Nephrology: CJASN
https://read.qxmd.com/read/26912549/bone-disease-after-kidney-transplantation
#5
REVIEW
Antoine Bouquegneau, Syrazah Salam, Pierre Delanaye, Richard Eastell, Arif Khwaja
Bone and mineral disorders occur frequently in kidney transplant recipients and are associated with a high risk of fracture, morbidity, and mortality. There is a broad spectrum of often overlapping bone diseases seen after transplantation, including osteoporosis as well as persisting high- or low-turnover bone disease. The pathophysiology underlying bone disorders after transplantation results from a complex interplay of factors, including preexisting renal osteodystrophy and bone loss related to a variety of causes, such as immunosuppression and alterations in the parathyroid hormone-vitamin D-fibroblast growth factor 23 axis as well as changes in mineral metabolism...
July 7, 2016: Clinical Journal of the American Society of Nephrology: CJASN
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