Skoči na glavni sadržaj

Ostalo

Erythrocytosis in a Hemodialysis Patient Treated with Iron Sucrose

Nikolina Bašić-Jukić
Bruna Brunetta
Martina Blažev
Iva Blajić
Nikolina Dumančić
Petar Kesi


Puni tekst: engleski pdf 58 Kb

str. 385-388

preuzimanja: 785

citiraj


Sažetak

A 59-year-old Caucasian male started intermittent hemodialysis in March 1995 for the treatment of end-stage renal disease of unknown etiology. In December 2002, he started receiving parenteral iron sucrose, 100 mg every two weeks, for iron deficiency. He did not receive erythropoietin. One month later he experienced severe pruritus. Blood analysis revealed erythrocytosis. Iron therapy was discontinued immediately, and four venepunctures were performed to avoid thrombosis of AV fistula. Malignant disease was excluded. It was decided to apply an angiotensin convertase enzyme inhibitor (ACEi), ramipril, in a dose of 2.5 mg/day. However, the patient developed severe cough as a side effect of ramipril and was
switched to an angiotensin receptor type II antagonist (AAR), losartan, in a dose of 25 mg/day. While the patient was prone to hypotension during the dialysis sessions, losartan was administered every evening at bedtime. One month after the introduction of AAR, a stable hemoglobin level was achieved. On control MSCT six months later, there was no sign of malignant disease. Oral ACEi and AAR are appropriate treatment in the control of erythrocytosis in dialysis patients.

Ključne riječi

Hemodialysis; Erythrocytosis; Losartan; Ramipril

Hrčak ID:

14562

URI

https://hrcak.srce.hr/14562

Datum izdavanja:

1.12.2004.

Podaci na drugim jezicima: hrvatski

Posjeta: 1.974 *