BACKGROUND: : Chronic allograft nephropathy (CAN) is characterized by loss of parenchymal perfusion. We applied therefore the novel parameter Tissue Pulsatility Index (TPI) to quantify transplant perfusion in the long-term surveillance of renal transplants. METHODS: : Color Doppler sonographic videos of renal transplants from 38 renal transplant recipients were recorded under defined conditions. TPI was calculated as ratio of the difference of mean systolic and diastolic velocities of the entire region and the average velocity. RESULTS: : TPI was significantly different between the proximal and distal cortical layers (1.12 vs. 1.56, respectively P=0.000). In patients with elevated creatinine as a measure of compromised function, significantly (P=0.016) higher values (TPI=1.70) were found at distal cortical level compared to patients with normal creatinine (TPI=1.34). After transplantation, TPI rises significantly: 1.10 in 0-1 years vs. 1.41 in 1-2.9 years, P=0.002; 1.10 in 0-1 years vs. 1.37 in 3-4.9 years, P=0.000; 1.10 in 0-1 years vs. 1.31 in 7-8.9 years, P=0.049). TPI declines later on in our population to significantly lowered values in the group more than 9 years after transplantation (1.10 in 0-1 years vs. 0.94 in >9 years, P=0.044). CONCLUSION: : With the novel TPI, we could demonstrate significant differences between proximal and distal cortical perfusion, between compromised and well-functioning transplants, and could observe significant changes of transplant perfusion at various points at the posttransplantation time scale.
BACKGROUND: : Chronic allograft nephropathy (CAN) is characterized by loss of parenchymal perfusion. We applied therefore the novel parameter Tissue Pulsatility Index (TPI) to quantify transplant perfusion in the long-term surveillance of renal transplants. METHODS: : Color Doppler sonographic videos of renal transplants from 38 renal transplant recipients were recorded under defined conditions. TPI was calculated as ratio of the difference of mean systolic and diastolic velocities of the entire region and the average velocity. RESULTS: : TPI was significantly different between the proximal and distal cortical layers (1.12 vs. 1.56, respectively P=0.000). In patients with elevated creatinine as a measure of compromised function, significantly (P=0.016) higher values (TPI=1.70) were found at distal cortical level compared to patients with normal creatinine (TPI=1.34). After transplantation, TPI rises significantly: 1.10 in 0-1 years vs. 1.41 in 1-2.9 years, P=0.002; 1.10 in 0-1 years vs. 1.37 in 3-4.9 years, P=0.000; 1.10 in 0-1 years vs. 1.31 in 7-8.9 years, P=0.049). TPI declines later on in our population to significantly lowered values in the group more than 9 years after transplantation (1.10 in 0-1 years vs. 0.94 in >9 years, P=0.044). CONCLUSION: : With the novel TPI, we could demonstrate significant differences between proximal and distal cortical perfusion, between compromised and well-functioning transplants, and could observe significant changes of transplant perfusion at various points at the posttransplantation time scale.
Authors: Andrzej Paweł Wieczorek; Magdalena Maria Woźniak; Aleksandra Stankiewicz; Giulio Aniello Santoro; Michał Bogusiewicz; Tomasz Rechberger; Jakob Scholbach Journal: World J Urol Date: 2011-07-28 Impact factor: 4.226
Authors: Magdalena M Woźniak; Thomas M Scholbach; Jakob Scholbach; Agata Pawelec; Paweł Nachulewicz; Andrzej P Wieczorek; Agnieszka Brodzisz; Maria M Zajączkowska; Halina Borzęcka Journal: Arch Med Sci Date: 2015-05-29 Impact factor: 3.318