PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY TREATMENT OF RENAL TRANSPLANT ARTERY STENOSIS
- 1 December 1982
- journal article
- research article
- Published by Wolters Kluwer Health in Transplantation
- Vol. 34 (6) , 339-343
- https://doi.org/10.1097/00007890-198212000-00005
Abstract
Since June 1979, percutaneous transluminal angioplasty (PTA) has been the procedure of choice for renal transplant artery stenosis (RTAS) at the Hospital of the University of Pennsylvania. Of 241 renal allograft recipients, 17 (7%) when studied by arteriogram because of suspected RTAS proved to have significant stenosis (the mean reduction in luminal width for the group being 68%) and underwent PTA. RTAS was equally prevalent in cadaver and related kidney allografts and was no less common in HLA-identical related donor grafts, arguing against the importance of immune factors in etiology. RTAS was equally prevalent whether the anastomotic technique was end to end or end to side. However, when RTAS occurred after end to side anastomoses, it was usually postanastomotic. Fifteen of 17 of the attempts at dilation by PTA were successful by angiographic analysis. Thirteen of the 15 successfully dilated patients had long-term allograft survival and in all of these instances blood pressure (BP) was decreased after PTA. After a mean of 67 weeks, BP decreased from a systolic of 184 ± 24 mm Hg pre-PTA to 135 ± 15 mm Hg (P < 0.001) and from a diastolic of 115 ± 10 mm Hg pre-PTA to 87 ± 11 mm Hg (P < 0.001). The majority of patients continue to require antihypertensive drugs but in a less vigorous regimen than pre-PTA. Serum creatinine level fell following PTA from 1.9 ± 0.6 to 1.7 ± 0.5 mg/100 ml (P < 0.01). Repeat angiographic study was done in nine patients, an average of 61 weeks after PTA, and no recurrent RTAS was identified. Three minor complications of PTA occurred but none led to long-term sequelae. Thus, we believe PTA of RTAS is relatively safe, carrying less mortality and morbidity than operative treatment, and is capable of improving BP control and renal allograft function.This publication has 6 references indexed in Scilit:
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