| Literature DB >> 21559256 |
Polytimi Leonardou1, Sofia Gioldasi, Paris Pappas.
Abstract
Transplant renal artery stenosis (TRAS) is a well-known cause of posttransplant hypertension accompanied by possible graft dysfunction and is potentially curable when is diagnosed early. Colour Doppler Ultrasonography (CDU) is the screening procedure of choice in most studies whereas some centers employ Magnetic Resonance Angiography (MRA), if available. Although both CDU and MRA can arouse suspicion of disease in less symptomatic cases, angiographic techniques are essential for confirmation of TRAS. Percutaneous Transluminal Angioplasty (PTA) is a good and widespread therapeutic approach for the treatment of TRAS due to its acceptable complication rate and high technical success rate. The purpose of this paper is to assess the safety and efficacy of PTA in the treatment of TRAS, to compare the long-term outcomes between different reports, and to examine the role of PTA with stenting in inhibiting recurrence of the disease.Entities:
Year: 2011 PMID: 21559256 PMCID: PMC3087892 DOI: 10.1155/2011/693820
Source DB: PubMed Journal: J Transplant ISSN: 2090-0007
Figure 1(a) Anastomotic transplant renal artery stenosis. (b) Postpercutaneous transluminal angioplasty and stenting image.
Figure 2(a) Transplant renal artery stenosis. (b) Postpercutaneous transluminal angioplasty and stenting image.
Figure 3(a) Transplant renal artery stenosis and postbiopsy arteriovenous fistula. (b) Postpercutaneous transluminal angioplasty and stenting and post-embolization image.
Studies published over the last decade presenting transplant renal artery stenosis treated by percutaneous transluminal angioplasty and stenting.
| Study (year) | Number of patients | Technical success (%) | Clinical Success (%)* | Follow-up (mean; months) | Complications related to the procedure (%) |
|---|---|---|---|---|---|
| Ghazanfar et al. (2011) [ | 44 | 100 | 86 | 60 | —** |
| Saratnahaei et al. (2010) [ | 9 | 100 | 77.7 | 17.3 | — |
| Henning et al. (2009) [ | 13 | 92.3 | Not mentioned | 33.15 | — |
| Hagen et al. (2009) [ | 24 | 93 | 75 | 3 | 14 |
| Pappas et al. (2008) [ | 22 | 100 | 91 | 29.5 | — |
| Peregrin et al. (2008) [ | 55 | 88 | 65 | 36 | 25.5 |
| Geddes et al. (2008) [ | 27 | 100 | 88.8 | 60 | 7.4 |
| Valpreda et al. (2008) [ | 30 | 100 | 80 | 85.2 | 2.9 |
| Polak et al. (2006) [ | 7 | 100 | 83.3 | 25.3 | — |
| Audard et al. (2006) [ | 29 | 93.1 | 67.2 | 148 | 10.3 |
| Salvadori et al. (2005) [ | 26 | 100 | 76.3 | 43.3 | — |
| Voiculescu et al. (2005) [ | 31 | 90.3 | 75.5 | 45.2 | 12.9 |
| Beecroft et al. (2004) [ | 17 | 100 | 94 | 27 | 10.5 |
| Patel et al. (2001) [ | 17 | 94 | 82 | 26.9 | — |
*Estimated as significant clinical benefit or good graft function during the whole follow-up period.
**No procedure-related complication mentioned.