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Acute antibody-mediated rejection of the kidney transplant - experience of a single center in Croatia (CROSBI ID 204014)

Prilog u časopisu | stručni rad

Orlić, Lidija ; sladoje-Martinović, Branka ; Mikolašević, Ivana ; Pavletić-Peršić, Martina ; Bubić, Ivan ; Jelić, Ita ; Rački, Sanjin Acute antibody-mediated rejection of the kidney transplant - experience of a single center in Croatia // Medicinski glasnik Ljekarske komore Zeničko-dobojskog kantona, 11 (2014), 1; 138-144

Podaci o odgovornosti

Orlić, Lidija ; sladoje-Martinović, Branka ; Mikolašević, Ivana ; Pavletić-Peršić, Martina ; Bubić, Ivan ; Jelić, Ita ; Rački, Sanjin

engleski

Acute antibody-mediated rejection of the kidney transplant - experience of a single center in Croatia

ABSTRACT Aim To describe the experience of the Department of Nephrology and Dialysis, University Hospital Rijeka, Croatia, in the treatment of patients with acute humoral rejection (AHR) of kidney transplant by using high dose of intravenous immunoglobulin (IVIG) alone and as a first line treatment. Methods Eight kidney transplant recipients in whom the AHR appeared at different time after the transplantation were reported. At the time of transplantation cross-match in all patients was negative for both T and B cells. At the time of presentation, all patients had signs of renal allograft dysfunction and the rejection was proven by biopsy of the kidney transplant with positive C4d- staining and histopathological evidence of antibody- mediated injury. Early rejection was considered within 180 days after the transplantation and the late one 180 days after the transplantation. In two cases plasmapheresis (PAF) with albumin as replacement fluid was performed. Plasma exchange was done with a 35 mL/kg/body weight volume exchange with albumin for six times. Results Acute humoral rejection was classified as early in three patients and in five as late one. In two patients PAF had been performed as the first line treatment. After the completion of PAF, recuperation of severe graft dysfunction was incomplete and in addition IVIG (as a single dose of 2.0 g/kg) was administered to these patients. In six patients IVIG as a single dose of 2.0 g/kg was applied as the first line treatment. Conclusion Usage of high dose IVIG in the treatment of the acute humoral rejection is efficient, safe and relatively well tolerated.

graft rejection ; imunosupresion ; recommendations ;

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Podaci o izdanju

11 (1)

2014.

138-144

objavljeno

1840-0132

Povezanost rada

Kliničke medicinske znanosti

Indeksiranost