Polycystic kidney disease: etiology, pathogenesis, and treatment

JR Martinez, JJ Grantham - Disease-a-month, 1995 - Elsevier
Once viewed as hopelessly incurable disorders and the dustbin for careers in academic
medicine, the polycystic kidney diseases have emerged as prime targets of …

Medical therapy with tranexamic acid in autosomal dominant polycystic kidney disease patients with severe haematuria

R Peces, A Aguilar, C Vega, E Cuesta… - Nefrología (English …, 2012 - revistanefrologia.com
Antecedentes: En la poliquistosis renal autosómica dominante (PQRAD), la hematuria
macroscópica por la rotura de quistes renales es una manifestación habitual, que puede ser …

[HTML][HTML] Autosomal dominant polycystic kidney disease

CL Chow, ACM Ong - Clinical medicine, 2009 - ncbi.nlm.nih.gov
Table 2 lists the investigations used in assessing ADPKD patients. New unified diagnostic
ultrasound criteria for at-risk PKD1 and PKD2 individuals have recently been reported …

Treatment of persistent gross hematuria with tranexamic acid in autosomal dominant polycystic kidney disease

Q Yao, M Wu, J Zhou, M Zhou, D Chen, L Fu… - Kidney and Blood …, 2017 - karger.com
Abstract Background/Aims: In this retrospective study we aimed to compare the effect of
tranexamic acid (TXA) vs etamsylate, two hemostatic agents, on hematuria duration in …

Tranexamic acid treatment of life‐threatening hematuria in polycystic kidney disease

T AlAmeel, M West - International journal of nephrology, 2011 - Wiley Online Library
A 41‐year‐old woman with autosomal dominant polycystic kidney disease had chronic
kidney disease class IV. She presented 10 days postpartum with a 4‐day history of severe …

A successful treatment of life-threatening bleeding from polycystic kidneys with antifibrinolytic agent tranexamic acid

B Vujkovac, M Sabovic - Blood coagulation & fibrinolysis, 2006 - journals.lww.com
We describe a successful treatment of a severe, persistent bleeding from both kidneys in a
patient with autosomal dominant polycystic kidney disease (ADPKD) with tranexamic acid …

[PDF][PDF] Tratamiento eficaz de la arteriolopatía urémica calcificante con bifosfonatos

JV Torregrosa, CE Durán, X Barros, M Blasco… - Nefrología …, 2012 - SciELO Espana
TORREGROSA, José V. et al. Tratamiento eficaz de la arteriolopatía urémica calcificante
con bifosfonatos. Nefrología (Madr.)[online]. 2012, vol. 32, n. 3, pp. 329-334. ISSN 0211 …

Traumatic hematuria in patients with polycystic kidney disease

AJP Klein, RA Kozar, LJ Kaplan - The American Surgeon, 1999 - journals.sagepub.com
Autosomal dominant polycystic kidney disease (PKD) is the most prevalent hereditary
disorder in this country and a common cause of chronic renal failure. Patients frequently …

Autosomal dominant polycystic kidney disease, incidental finding with trauma: case report and review of the literature

NJ Gildenhuys, A Van der Merwe - African Journal of Urology, 2017 - ajol.info
Introduction: Pre-existing renal lesions predispose kidneys to effects of otherwise
insignificant blunt trauma, and may uncommonly present as an incidental finding in the …

Hemostatic therapy revisited

JC Horrow - Anesthesiology clinics of North America, 1994 - Elsevier
No benefit accrues from the prophylactic administration of desmopressin to limit surgical
bleeding in patients with normal hemostasis. This applies to many different kinds of surgical …