American Journal of Nephrology

Clinical Study

A New Treatment forInterdialytic Hyperkalemia – The Use of Fosinopril Sodium

Mousa D. · Rassoul Z. · Popovich W. · Hassan A. · Margate V. · Hawas F. · Suleiman M. · Al Khader A.

Author affiliations

Department of Nephrology, Riyadh Military Hospital, Riyadh, Saudi Arabia

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Am J Nephrol 1999;19:395–399

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Article / Publication Details

First-Page Preview
Abstract of Clinical Study

Published online: June 18, 1999
Issue release date: May – June

Number of Print Pages: 5
Number of Figures: 1
Number of Tables: 2

ISSN: 0250-8095 (Print)
eISSN: 1421-9670 (Online)

For additional information: https://www.karger.com/AJN

Abstract

Fosinopril sodium is the first of the phosphinic acid class of angiotensin-converting enzyme inhibitors (ACEI). It is used as an antihypertensive agent, but differs from other ACEI in its dual routes of excretion (liver and kidney), and less incidence of hyperkalemia and cough. We conducted a study in known chronic hemodialysis patients who developed interdialytic hyperkalemia in spite of other treatments to control hyperkalemia. We used fosinopril in this group of patients to assess the effect of fosinopril on serum potassium (K) levels. Twenty-four patients were given fosinopril 10 mg at 18:00 h daily for 8 weeks. K levels were measured before and after each dialysis treatment. Interdialytic weight gains were recorded. The average pretrial potassium level was 6.57 mmol/l (± 0.47), and the posttrial level was 5.34 (± 0.76); p ≤ 0.0001. No statistically significant interdialytic weight gain or reduction occurred. No first dose hypertensive effect or cough were reported. We have found the use of fosinopril to be successful in lowering predialysis serum K levels in hyperkalemic dialysis patients.




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References

  1. Singhvi SM, Duchin KL, Morrison RA, Williard DA, Everett DW, Frantz M: Disposition of fosinopril sodium in healthy subjects. Br J Clin Pharmacol 1988;25:9–15.
    External Resources
  2. Duchin KL: Clinical pharmacology of fosinopril. Drug Invest 1995;3(suppl 4):12–17.
  3. Germino FW, Lastra J, Pool P, Punzi H, Spinowitz B, Smith W, Mills D: An open label pilot study evaluating cough profile of fosinopril sodium in hypertensive patients with documented cough associated with previous ACE inhibitor monotherapy (abstract). Am J Hypertens 1992;6:113A.
  4. David D, Jallad N, Germino W, Willett M, de Silva J, Weidner S, Mills D: A comparison of the cough profile of fosinopril and enalapril in hypertensive patients with a history of ACE inhibitor-associated cough. Am J Ther 1995;2:806–813.
    External Resources
  5. Duchin KL, Kripalani K, Kramer P, Sica D: Disposition and pharmacodynamics of fosinopril sodium and its diacid in hemodialysis patients (abstract). Kidney Int 1989;35:245.
  6. Sica D, Davis J, Fakhry I, Nunley J: Fosinopril sodium pharmacokinetic and pharmacodynamics in CAPD (abstract). Kidney Int 1989;35:277.
  7. Textor SC, Bravo EL, Fouad FM, Terazi RC: Hyperkalemia in azotemic patients during angiotensin-converting enzyme inhibition and aldosterone reduction with captopril. Am J Med 1982;73:719–725.
    External Resources
  8. Atlas SA, Case DB, Sealey JE, Laragh JH, McKinstry DN: Interruption of the renin-angiotensin system in hypertensive patients by captopril induces sustained reduction in aldosterone secretion, potassium retention, and natriuresis. Hypertension 1979;1:274–280.
    External Resources
  9. Mulrow PJ, Kusano E, Baba K, Shier D, Doi Y: Adrenal renin: A possible local hormonal regulator of aldosterone production. Yale J Biol Med 1989;62:503–510.
    External Resources
  10. Schlueter W, Keilani T, Batlle DC: Tissue renin angiotensin systems: Theoretical implications for the development of hyperkalemia using angiotensin-converting enzyme inhibitors. Am J Med Sci 1994;307(suppl 1):81–86.
  11. Keilani T, Schlueter W, Batlle DC: Selected aspects of ACE inhibitor therapy for patients with renal disease: Impact on proteinuria, lipids and potassium. J Clin Pharmacol 1995;35:87–97.
  12. Keilani T, Schlueter W, Molteni A, Batlle DC: Converting enzyme inhibition with fosinopril does not suppress plasma aldosterone and may not cause hyperkalemia despite moderate renal impairment. J Am Soc Nephrol 1991;2:281.
  13. Panese S, Martin R, Virginillo M: Mechanism of enhanced cellular potassium secretion in man with chronic renal failure. Kidney Int 1987;31:1377–1382.
    External Resources
  14. Al Khader AA, Al Hasani MK, Dhar JM, Suleiman M: Effect of diet during Ramadan on patients on chronic hemodialysis. Saudi Med J 1991;12:30–31.

Article / Publication Details

First-Page Preview
Abstract of Clinical Study

Published online: June 18, 1999
Issue release date: May – June

Number of Print Pages: 5
Number of Figures: 1
Number of Tables: 2

ISSN: 0250-8095 (Print)
eISSN: 1421-9670 (Online)

For additional information: https://www.karger.com/AJN


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