Literature DB >> 16199929

Life-threatening hyperkalemia during a combined therapy with the angiotensin receptor blocker candesartan and spironolactone.

Hideki Fujii1, Hajime Nakahama, Fumiki Yoshihara, Satoko Nakamura, Takashi Inenaga, Yuhei Kawano.   

Abstract

We describe a hypertensive nephrosclerosis patient presenting with severe hyperkalemia due to a combination therapy of the angiotensin receptor blocker (ARB) candesartan and spironolactone despite mildly decreased renal function. Recently, ARBs are replacing the ACE inhibitors. The combined therapy with ARB and spironolactone will eventually become the standard regimen. The strict attention and close monitoring of serum potassium should be mandatory in combination therapy to prevent hyperkalemia. Assessment of trans-tubular potassium gradient (TTKG) and fractional excretion of potassium (FEK) before starting the therapy would help in identifying the patients at higher risk of developing hyperkalemia. Co-administration of thiazide or loop diuretics is recommended to reduce the risk of hyperkalemia.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16199929

Source DB:  PubMed          Journal:  Kobe J Med Sci        ISSN: 0023-2513


  4 in total

Review 1.  Management of hyperkalaemia consequent to mineralocorticoid-receptor antagonist therapy.

Authors:  Sara S Roscioni; Dick de Zeeuw; Stephan J L Bakker; Hiddo J Lambers Heerspink
Journal:  Nat Rev Nephrol       Date:  2012-10-16       Impact factor: 28.314

2.  A study of tubular potassium secretory capacity in older patients with hyperkalaemia.

Authors:  C Mc Greevy; J Horan; D Jones; K Biswas; Y M O'Meara; E C Mulkerrin
Journal:  J Nutr Health Aging       Date:  2008-02       Impact factor: 4.075

3.  Maximizing diuretic therapy in resistant hypertension.

Authors:  Joel Handler
Journal:  J Clin Hypertens (Greenwich)       Date:  2007-10       Impact factor: 3.738

4.  Commentary in support of a highly effective hypertension treatment algorithm.

Authors:  Joel Handler
Journal:  J Clin Hypertens (Greenwich)       Date:  2013-08-07       Impact factor: 3.738

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.