CELLULAR VERSUS VASCULAR REJECTION IN TRANSPLANT KIDNEYS - CORRELATION OF RADIONUCLIDE AND DOPPLER STUDIES WITH HISTOLOGY

Citation
Am. Alnahhas et al., CELLULAR VERSUS VASCULAR REJECTION IN TRANSPLANT KIDNEYS - CORRELATION OF RADIONUCLIDE AND DOPPLER STUDIES WITH HISTOLOGY, Nuclear medicine communications, 14(9), 1993, pp. 761-765
Citations number
NO
Categorie Soggetti
Radiology,Nuclear Medicine & Medical Imaging
ISSN journal
01433636
Volume
14
Issue
9
Year of publication
1993
Pages
761 - 765
Database
ISI
SICI code
0143-3636(1993)14:9<761:CVVRIT>2.0.ZU;2-G
Abstract
The presence of two distinct subtypes of renal allograft rejection are well documented by histological studies. The differentiation between vascular rejection (VR) and cellular rejection (CR) is essential for p roper management by avoiding the need for unnecessary and potentially harmful immunosuppressive treatment of VR. A histological pattern with features that are similar and confusable with some cases of rejection may be seen in cyclosporin A toxicity (CyT). To evaluate the efficien cy of Guy's perfusion index (GPI) and the Doppler pulsatility index (D PI) in differentiating these two histological subtypes, a prospective study was designed in which a total of 140 radionuclide tests and 133 ultrasounds scans performed on the same day on 58 patients during the first 3 months post-transplant were analysed, and the results correlat ed with the histological findings of 84 renal biopsies. Results show t hat the GPI had a sensitivity of 86.5% and a specificity of 94% in dif ferentiating VR and CyT from CR, while the DPI had values of 83% and 6 9%, respectively. Chi-squared analysis showed a higher significant ass ociation between the GPI and histology (P < 0.0001) compared to that o f the DPI and histology (P < 0.005), while Youden's index (J) showed a significant difference (P < 0.05) between GPI and DPI. It is conclude d that GPI is more sensitive and specific than DPI in differentiating transplants that are well perfused from those with poor perfusion (VR and CyT).