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1.
Transplantation ; 65(2): 253-5, 1998 Jan 27.
Article in English | MEDLINE | ID: mdl-9458024

ABSTRACT

BACKGROUND: Mothers treated with cyclosporine (CsA) have previously not been allowed to breast-feed due to the reported accumulation of the drug in breast milk. The purpose of this study was to evaluate the consequences of allowing breast-feeding. METHODS: Seven infants were breast-fed by mothers who had undergone kidney transplantation alone (n=5) or simultaneous kidney and pancreas transplants (n=2). In addition to CsA, all mothers received prednisolone at 5-7.5 mg/day and six mothers received azathioprine at 50-100 mg. CsA concentration was measured in the whole blood of mothers and babies and in breast milk. Serum creatinine was measured in babies 1 week after birth and after 4-12 months of breast-feeding. RESULTS: Blood CsA levels ranged from 55 to 130 ng/ml in mothers (12-hr trough), 50 to 227 ng/ml in breast milk (mean for each woman), and was below the detection limit of 30 ng/ml in all infants. Breast milk concentration ranged from 87 to 440 ng/ml in 16 samples obtained at various time points from one mother. Infants' serum creatinine ranged from 25 to 54 micromol/L at 1 week after birth and 23-52 micromol/L after breast-feeding. All babies thrived. CONCLUSIONS: Breast-fed infants of mothers treated with CsA received less than 300 microg per day of CsA and absorbed undetectable amounts. There were no demonstrable nephrotoxic effects or other side effects. Thus, women with kidney transplants could be allowed to breast-feed.


Subject(s)
Breast Feeding , Cyclosporine/pharmacokinetics , Immunosuppression Therapy , Immunosuppressive Agents/pharmacokinetics , Kidney Transplantation , Adult , Azathioprine/therapeutic use , Creatinine/blood , Cyclosporine/analysis , Cyclosporine/blood , Cyclosporine/therapeutic use , Female , Glucocorticoids/therapeutic use , Humans , Immunosuppressive Agents/analysis , Immunosuppressive Agents/blood , Immunosuppressive Agents/therapeutic use , Infant , Infant, Newborn , Milk, Human/chemistry , Pancreas Transplantation , Prednisolone/therapeutic use
2.
Scand J Urol Nephrol ; 28(1): 17-20, 1994 Mar.
Article in English | MEDLINE | ID: mdl-8009187

ABSTRACT

Calcium channel blocking agents (CCB) differ in molecular structure and effects. Each must therefore be evaluated separately. Out of 139 patients who received cadaveric kidney transplants between March 1990 and December 1991 22 were treated with the CCB agent felodipine as antihypertensive therapy on admission and post transplant. The early function of their grafts was compared with that of grafts to patients not treated with any CCB agent pre or post transplant (n = 38). There were no other significant differences in patient or donor characteristics. In the felodipine treated group, 18/22 showed immediate onset of graft function vs 20/38 in the non CCB group (p = 0.02). Dialysis post transplant was required by one felodipine-treated patient vs 12 in the non CCB group. Serum creatinine on day 7 was lower in felodipine treated patients, median 155 vs 259 mumol/l. Felodipine treatment did not seem to cause any significant interaction with cyclosporin A (CyA). The frequency and severity of acute rejection did not differ between the groups.


Subject(s)
Felodipine/administration & dosage , Kidney Failure, Chronic/surgery , Kidney Transplantation/physiology , Kidney/blood supply , Postoperative Complications/prevention & control , Premedication , Adolescent , Adult , Aged , Blood Flow Velocity/drug effects , Blood Flow Velocity/physiology , Cadaver , Creatinine/blood , Cyclosporine/administration & dosage , Cyclosporine/adverse effects , Felodipine/adverse effects , Female , Glomerular Filtration Rate/drug effects , Glomerular Filtration Rate/physiology , Graft Rejection/physiopathology , Graft Rejection/prevention & control , Humans , Kidney Failure, Chronic/physiopathology , Kidney Function Tests , Male , Middle Aged , Postoperative Complications/physiopathology , Regional Blood Flow/drug effects , Regional Blood Flow/physiology , Renal Dialysis , Retrospective Studies
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