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Condition: Proteinuria
Therapy: Dialysis
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Total 461 results found since Jan 2013.
SARS-CoV-2 infection: a possible trigger for the recurrence of IgA nephropathy after kidney transplantation?
J Nephrol. 2023 Jun 21. doi: 10.1007/s40620-023-01684-y. Online ahead of print.ABSTRACTImmunoglobulin A nephropathy, the most common primary glomerulonephritis worldwide, is a leading cause of chronic kidney disease and end-stage kidney failure. Several cases of immunoglobulin A nephropathy relapse in native kidneys have been described after COVID-19 vaccination or SARS-CoV-2 infection. Here, we report the case of a 52-year-old kidney transplant recipient who had a stable transplant function for more than 14 years, with a glomerular filtration rate above 30 ml/min/1.73 m2. The patient had been vaccinated against COVID-19 f...
Source: Journal of Nephrology - June 21, 2023 Category: Urology & Nephrology Authors: Eric Jankowski Mandy Schlosser Thorsten Wiech Gunter Wolf Martin Busch Source Type: research
Gender Difference of Blood Pressure Control Rate and Clinical Prognosis in Patients With Resistant Hypertension: Real-World Observation Study
CONCLUSION: In resistant hypertension, men were younger than women, but end-organ damage was more common and the risk of cardiovascular event was higher. More intensive cardiovascular prevention strategies may be required in male patients with resistant hypertension.PMID:37096308 | PMC:PMC10125792 | DOI:10.3346/jkms.2023.38.e124
Source: J Korean Med Sci - April 25, 2023 Category: General Medicine Authors: Hyung Joon Joo Yunjin Yum Yong Hyun Kim Jung-Woo Son Sung Hea Kim Seonghoon Choi Seongwoo Han Mi-Seung Shin Jin-Ok Jeong Eung Ju Kim Working Group on Hypertension Complication Source Type: research
Persistent acidosis and chronic kidney disease in a patient with type 1 glycogen storage disease
Clin Nephrol. 2023 Mar 5. doi: 10.5414/CN111005. Online ahead of print.ABSTRACTType 1 glycogen storage disease (GSDI) is a rare autosomal recessive disorder caused by glucose-6-phosphatase (G6Pase) deficiency. We discuss a case of a 29-year-old gentleman who had GSDI with metabolic complications of hypoglycemia, hypertriglyceridemia, hyperuricemia, and short stature. He also suffered from advanced chronic kidney disease, nephrotic range proteinuria, and hepatic adenomas. He presented with acute pneumonia and refractory metabolic acidosis despite treatment with isotonic bicarbonate infusion, reversal of hypoglycemia, and la...
Source: Clinical Nephrology - March 5, 2023 Category: Urology & Nephrology Authors: Kai Xiong Lim Yan Mee Law Weiwen Guo Source Type: research
Cardiorenal Syndrome in the Hospital
Clin J Am Soc Nephrol. 2023 Jan 13. doi: 10.2215/CJN.0000000000000064. Online ahead of print.ABSTRACTThe cardiorenal syndrome refers to a group of complex, bidirectional pathophysiological pathways involving dysfunction in both the heart and kidney. Upward of 60% of patients admitted for acute decompensated heart failure have CKD, as defined by an eGFR of <60 ml/min per 1.73 m2. CKD, in turn, is one of the strongest risk factors for mortality and cardiovascular events in acute decompensated heart failure. Although not well understood, the mechanisms in the cardiorenal syndrome include venous congestion, arterial underfi...
Source: Clinical Journal of the American Society of Nephrology : CJASN - February 14, 2023 Category: Urology & Nephrology Authors: Wendy McCallum Mark J Sarnak Source Type: research
Evaluating Kidney Function Decline in Children with Chronic Kidney Disease Using a Multi-Institutional Electronic Health Record Database
CONCLUSIONS: In large-scale real-world data for children with CKD, disease etiology, albuminuria, hypertension, age, male sex, lower eGFR, and greater medical complexity at start of follow-up were associated with more rapid decline in kidney function.PMID:36754006 | DOI:10.2215/CJN.0000000000000051
Source: Clinical Journal of the American Society of Nephrology : CJASN - February 8, 2023 Category: Urology & Nephrology Authors: Caroline A Gluck Christopher B Forrest Amy Goodwin Davies Mitchell Maltenfort Jill R Mcdonald Mark Mitsnefes Vikas R Dharnidharka Bradley P Dixon Joseph T Flynn Michael J Somers William E Smoyer Alicia Neu Collin A Hovinga Amy L Skversky Thomas Eissing An Source Type: research
A case of membranous nephropathy with microspherular deposits progressing to collapsing nephropathy and dialysis dependency, but with full recovery following immunosuppression
We report a case presenting with severe nephrotic syndrome and pathological features of collapsing glomerulopathy. This is the first case we are aware of that progressed to requiring dialysis. The patient received rituximab and corticosteroids. She has now been off dialysis for over a year with both serum creatinine and urine protein-creatinine ratio returning to baseline.PMID:36708206 | DOI:10.5414/CN110998
Source: Clinical Nephrology - January 28, 2023 Category: Urology & Nephrology Authors: Matthew Sayer Samuel Pattle Paul J Phelan Christopher O C Bellamy Source Type: research
