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6.
Am J Nephrol ; 18(2): 101-4, 1998.
Article in English | MEDLINE | ID: mdl-9569950

ABSTRACT

This study was carried out to find out whether Ramadan fasting would affect the renal function in kidney transplant recipients with normal or impaired graft function. Twenty-three transplant recipients, 17 with a normal function and 6 with an impaired but stable function with plasma creatinine levels not exceeding 300 mmol/l, were included in this study. The mean posttransplant period was 2.0 (range 0.6-6.3) years. Urinary and serum biochemical parameters, ciclosporin A level, and hematocrit were checked weekly, during Ramadan as well as 1 week before and after. Statistical analysis showed no significant changes in all parameters before, during, and after Ramadan. In conclusion, our findings indicate that fasting during the month of Ramadan does not seem to be associated with any significant adverse effects in kidney transplant recipients with normal or impaired graft function and suggest that it is safe for those patients to fast during Ramadan after 1 year of renal transplantation.


Subject(s)
Fasting/physiology , Islam , Kidney Transplantation/physiology , Religion and Medicine , Adult , Biomarkers/blood , Biomarkers/urine , Cyclosporine/blood , Fasting/adverse effects , Female , Humans , Kidney/metabolism , Kidney/physiopathology , Male , Middle Aged , Potassium/blood
7.
Saudi Med J ; 19(2): 197-198, 1998 Mar.
Article in English | MEDLINE | ID: mdl-27701587

ABSTRACT

Full text is available as a scanned copy of the original print version.

8.
Am J Kidney Dis ; 29(4): 631-2, 1997 Apr.
Article in English | MEDLINE | ID: mdl-9100057

ABSTRACT

We report a 38-year-old man who developed systemic lupus erythematosus (SLE) 14 years after commencing regular hemodialysis. When he was initially diagnosed as having end-stage renal disease (ESRD) secondary to chronic glomerulonephritis, he did not have any clinical or serological criteria to suspect SLE. He did not receive, at any stage, any of the drugs known to cause SLE. He showed remarkable improvement after treatment with steroids and cyclophosphamide.


Subject(s)
Kidney Failure, Chronic/therapy , Lupus Erythematosus, Systemic/physiopathology , Renal Dialysis , Adult , Glomerulonephritis/complications , Humans , Kidney Failure, Chronic/etiology , Male
9.
Ren Fail ; 19(6): 771-80, 1997 Nov.
Article in English | MEDLINE | ID: mdl-9415934

ABSTRACT

Estimation of red cell ferritin (RCFer) may give a good indication of iron supply to the erythron and it may therefore be clinically useful for the detection of functional iron deficiency. In a cross-sectional study of hemodialysis patients on erythropoietin (EPO) therapy and regular oral iron we have compared the RCFer levels with conventional indicators of iron status. The patients studied, 19 female, 48 male, mean age 62 +/- 3.6 years (range 20-83 years) were characterized by the following mean parameters: aluminum 1.24 +/- 0.12 mumol/L, PTH 115.7 +/- 39 pg/mL, vitamin B12 626 +/- 71.2 ng/L, serum folate 18.8 +/- 2.2 micrograms/L, and hemoglobin 9.8 +/- 0.3 g/dL (range 7.3-12.4). The median serum ferritin (SF), RCFer, total iron binding capacity (TIBC), transferrin saturation (TS), and serum iron were 68 micrograms/L, 14.1 ag ferritin/red cell, 57 mumol/L, 20% and 11.5 mumol/L, respectively. Eleven patients had a reduced RCFer (< 7 ag ferritin/red cell), 5 had a SF of < 15 micrograms/L and 22 a TS of < 16%. The occurrence of functional iron deficiency was suggested by the presence of 10 subjects with reduced RCFer despite normal SF levels (15-240 micrograms/L). Four patients with reduced SF showed acceptable levels of RCFer, suggesting that some patients may maintain an adequate iron supply despite diminished iron stores. Despite oral iron therapy, a significant number of patients (63%) on regular hemodialysis remain relatively iron deficient with a serum ferritin of less than 100 micrograms/L. It has previously been proposed that oral iron provides adequate supplementation during increased demand caused by EPO stimulation. The present study has demonstrated overt iron deficiency in five subjects and suggests functional iron deficiency in a further seven (22% of total patients). We therefore conclude that oral iron therapy cannot maximize the response to EPO.


Subject(s)
Biomarkers/blood , Erythrocytes/chemistry , Ferritins/blood , Iron Deficiencies , Renal Dialysis/adverse effects , Administration, Oral , Adult , Aged , Aged, 80 and over , Aluminum/blood , Anemia, Hypochromic/blood , Anemia, Hypochromic/etiology , Cross-Sectional Studies , Erythropoietin/therapeutic use , Female , Folic Acid/blood , Hemoglobins/analysis , Humans , Iron/administration & dosage , Male , Middle Aged , Vitamin B 12/blood
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