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Objectives: Physiological management during pedi-atric renal transplants may affect outcomes secondary to intraoperative organ perfusion. Our goal was to investigate intraoperative factors affecting postope-rative renal function. We investigated whether mean arterial pressure, total intravenous fluids, central venous and invasive arterial pressure monitoring, and epidural analgesia would correlate with postoperative serum creatinine.
Materials And Methods: The design was a retrospective cohort study. Pediatric renal transplants performed from 2016 to 2022 were included, and 47 patients age <18 years were included. The primary outcome variables were creatinine levels at postoperative day 1 and day 30.
Results: There was a significant negative correlation between weight-adjusted mean arterial pressure after reperfusion and day 30 creatinine (r = -0.55; P < .001). There was also a significant negative correlation between transfused volume of red blood cells and day 30 creatinine (r = -0.73; P = .0068). Epidural catheter placement was associated with significantly lower median serum creatinine on day 1 (111 vs 248 μmol/L; P = .012) and lower mean serum creatinine on day 30 (62.5 ± 29.2 vs 92.5 ± 35.3 μmol/L; P = .011). Patients with epidural catheters received a significantly greater mean volume of intravenous fluids versus the nonepidural group (82.5 ± 23.4 vs 65.2 ± 25.7 mL/kg;P = .042). There was no correlation between total infused intravenous fluids and day 1 or day 30 postoperative serum creatinine. No correlation was found between central venous pressure monitoring, invasive arterial pressure monitoring, and posto-perative creatinine.
Conclusions: Mean arterial pressure after reperfusion, transfused volume of red blood cells, and epidural analgesia had a measurable effect on posttransplant kidney function. Variations in total infused intravenous fluids and the use of invasive hemodynamic moni-toring did not correlate with postoperative serum creatinine.
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http://dx.doi.org/10.6002/ect.2025.0058 | DOI Listing |
Zhong Nan Da Xue Xue Bao Yi Xue Ban
May 2025
Nursing Department, Third Xiangya Hospital, Central South University, Changsha 410013.
Objectives: End stage renal disease (ESRD) is a major disease that seriously threatens the health of young people, and kidney transplantation is an effective treatment method to improve its prognosis.Young ESRD patients at a critical stage of life development often face significant physical and psychological challenges while waiting for kidney transplantation. Their psychological state directly affects treatment compliance and transplantation outcomes.
View Article and Find Full Text PDFClin Transplant Res
September 2025
Division of Nephrology, Department of Internal Medicine, Kyung Hee University College of Medicine, Seoul, Korea.
Background: Calcineurin inhibitor (CNI) toxicity is a significant cause of graft dysfunction in kidney transplant recipients, yet distinguishing it from acute rejection (AR) and acute tubular necrosis (ATN) remains challenging. This study investigated the use of urinary mRNA biomarkers as a noninvasive tool for identifying CNI toxicity.
Methods: We retrospectively enrolled 110 kidney transplant recipients and classified them into four groups based on pathological findings: stable graft function (n=35), CNI toxicity (n=25), AR (n=30), and ATN (n=20).
Transplant Rev (Orlando)
September 2025
Nursing Department, Faculty of Health Sciences Başkent University, Ankara, Türkiye.
Transpl Immunol
September 2025
Molecular and Transplant Immunology Laboratory, Department of Transfusion Medicine (Blood Center), Medanta-The Medicity, Gurgaon, Haryana, India.
Over 60 % of kidney transplant candidates are non-sensitised while remaining 40 % are sensitised because of previous exposure to human alloantigens during previous transplants, blood transfusions, and pregnancy in women. Pre-transplant compatibility testing is mandatory prior to renal transplantation for detecting the presence of donor-specific antibodies (DSAs), which are associated with early hyperacute/acute and later chronic rejections. Initially, complement-dependent cytotoxicity crossmatch (CDCXM) was used as a traditional method for detecting preformed DSAs.
View Article and Find Full Text PDFAm J Transplant
September 2025
Institut de Transplantation Urologie Néphrologie (ITUN), CHU Nantes, Nantes, France; Centre de Recherche en Transplantation et Immunologie UMR1064, INSERM, Université de Nantes, Nantes, France. Electronic address:
A comprehensive analysis was performed on all consecutive biopsy-proven Thrombotic Microangiopathy (TMA) complicating kidney transplantation in the post C5 inhibitor era (from 2009) to identify pathological profiles, determine causes and establish risk factor associated with death-censored graft survival, in two French center. Pathological criteria were assessed according to the TMA Banff Working Group, followed by an unbiased analysis to identify distinct subgroups. 119 cases were identified, 8(6.
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