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Published on: July 3, 2013
[Effect of hypertension on function of the transplanted kidney--3 years follow-up]
Andrzej Oko1, Anna Olejnik, Iiona Idasiak-Piechocka
1Katedra i Klinika Nefrologii Akademii Medycznej w Poznaniu. aoko@usoms.poznan.pl
Insights
Maintaining controlled blood pressure (BP) in hypertensive kidney transplant recipients is crucial. Unsatisfactory BP control led to declining kidney function and cardiovascular events over three years.
Area of Science:
- Nephrology
- Immunology
- Cardiology
Context:
- Hypertension is a common complication after kidney transplantation.
- Aggressive blood pressure management is recommended post-transplant.
- Long-term effects of blood pressure control on graft function require further investigation.
Purpose:
- To compare kidney transplant function in hypertensive patients with satisfactory versus unsatisfactory blood pressure control.
- To evaluate the impact of blood pressure management on graft survival and cardiovascular events over three years.
Summary:
- This study followed 49 hypertensive kidney transplant patients for three years.
- Patients with satisfactory blood pressure control (below 160/90 mmHg) maintained stable graft function.
- Patients with unsatisfactory blood pressure control showed a significant increase in creatinine levels and experienced cardiovascular events.
Impact:
- Demonstrates the critical role of sustained blood pressure control in preserving kidney transplant function.
- Highlights the increased risk of graft deterioration and cardiovascular complications in poorly controlled hypertensive recipients.
- Informs clinical practice regarding intensified antihypertensive strategies in post-transplant care.
Abstract:
Hypertension accelerates the deterioration of the function of transplanted kidney. Aggressive control of blood pressure is recommended in post-transplant period when maintenance levels of the immunosuppressive drugs are achieved. The aim of this study was to compare the transplanted kidney function in two groups of the hypertensive patients matched for age, sex, HLA-mismatches, early post-transplant course, standard triple immunosuppression and hypotensive therapy during 3 years of follow-up. The mean through-levels of cyclosporine A in whole blood were similar in both groups and did not exceed 185 ng/ml. Group 1 consisted of 28 patients with satisfactory blood pressure (BP) control (arterial pressure below 160/90 mmHg) and group 2 consisted of 21 patients with unsatisfactory BP control. Slow but significant increase of the mean creatinine levels was observed in group 2 during 3 years of follow up, whereas in group 1 graft function remained stable. Cardiovascular events were observed only in group 2--stroke in one patient and death because of heart failure in one patient.
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