keyword
https://read.qxmd.com/read/25518545/-growth-retardation-in-children-with-chronic-renal-disease
#1
REVIEW
(no author information available yet)
Despite recent advances in the management of children with chronic renal disease (CRD), growth retardation remains its most visible comorbid condition. Growth retardation has adverse impact on morbidity and mortality rates, quality of life and education, and in adult patients on job family life, and independent leaving accomodation. Pathophysiology of impaired growth in CRD is complex and still not fully understood. The following complications are: anorexia, malnutrition, inflammation, decreased residual renal function, dialysis frequency and adequacy, renal anemia, metabolic acidosis, fluid/electrolyte imbalance, renal osteodistrophy, growth hormone (GH) and insulin-like growth factor-1 (IGF-1) resistance...
September 2014: Srpski Arhiv za Celokupno Lekarstvo
https://read.qxmd.com/read/23405977/pulmonary-hypertension-in-dialysis-patients
#2
REVIEW
George Kosmadakis, Didier Aguilera, Odette Carceles, Enrique Da Costa Correia, Ioannis Boletis
Pulmonary hypertension in end-stage renal disease patients is associated with significantly increased morbidity and mortality. The prevalence of pulmonary hypertension in dialysis patients is relatively high and varies in different studies from 17% to 49.53% depending on the mode of dialysis and other selection factors, such as the presence of other cardiovascular comorbidities. The etiopathogenic mechanisms that have been studied in relatively small studies mainly include arteriovenous fistula-induced increased cardiac output, which cannot be accomodated by, the spacious under normal conditions pulmonary circulation...
2013: Renal Failure
https://read.qxmd.com/read/20013598/-ab0-incompatible-kidney-transplantation-case-13-2009
#3
JOURNAL ARTICLE
Martina Guthoff, Dorothee Wernet, Wolfgang Steurer, Nils Heyne
UNLABELLED: PATIENT HISTORY AND CLINICAL FINDINGS: A 49-year old patient with chronic kidney disease was referred for evaluation of living donor kidney transplantation from his spouse in a blood group incompatible setting. CLINICAL INVESTIGATIONS: Patient blood group was 0, donor blood group was A, subtype A. recipient isoagglutinin titer against donor erythrocytes was 1:64. Crossmatch (CDC) and antibody screening were negative. There were no contraindications for living donor kidney transplantation from donor and recipient side...
December 2009: Deutsche Medizinische Wochenschrift
https://read.qxmd.com/read/19001812/rapid-accomodation-of-an-a1-renal-allograft-after-preconditioning-for-abo-incompatible-transplantation
#4
JOURNAL ARTICLE
Geoff Allen, Christopher E Simpkins, Dorry Segev, Daniel Warren, Karen King, Janis Taube, Jayme Locke, William Baldwin, Mark Haas, Raghu Chivukula, Robert A Montgomery
BACKGROUND: Successful ABO-incompatible (ABOi) kidney transplantation of non-A2 renal allografts requires preconditioning to reduce anti-blood group antibody to safe lev-els in order to avoid hyperacute rejection. Unfortunately, early post-transplant acute antibody-mediated rejection remains a problem in these patients and can result in rapid graft loss. A number of investigators have encountered ABOi recipients who have had no evidence of allograft injury in the setting of elevated titers of anti-ABO antibody, a protective phenomenon that has been termed 'accommodation'...
2009: Contributions to Nephrology
https://read.qxmd.com/read/16889538/histologic-findings-from-positive-crossmatch-or-abo-incompatible-renal-allografts-accomodation-or-chronic-allograft-injury
#5
EDITORIAL
B Sis, B Kaplan, P F Halloran
No abstract text is available yet for this article.
August 2006: American Journal of Transplantation
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