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Assessment of Renal Vascular Anatomy On Multi-Detector Computed Tomography in Living Renal Donors
Assessment of Renal Vascular Anatomy On Multi-Detector Computed Tomography in Living Renal Donors
Fig. 1. The 40-year-old female prospective renal donor. 3D volume-rendered CT and coronal maximum-intensity projection demonstrating three right-sided
(R1, R2, R3) and two left-sided (L1, L2) renal arteries.
the purposes of this study, initial assessment of all eligi- due to the presence of fibromuscular dysplasia in the
ble MDCTs was performed by two radiology residents right renal artery. In the other 2 subjects, the right kid-
(EC, BM). Subsequent review of all imaging by a fellow- ney was used due to surgeons’ preference.
ship-trained radiologist (MM) was performed. For image On the left, the distances between multiple arteries
analysis, thin slice (1 mm) multi-planar reformats were ranged from 1 to 43 mm, and on the right, they were 1
used with maximum-intensity-projection (10 mm) ren- to 84 mm (Tables 2 and 3).
dering used as an adjunct display where required. The median length of the right renal artery was
Parameters assessed in this study were as follows: 44 mm (IQR 28–60) and 34 mm (IQR 19–49) on the left.
Table 1. Breakdown of the number of renal arteries on either side and LEFT Kidney: 2 or more renal arteries, n = 47
whether they proceeded to donation
Total distance (mm)† Total Range (mm)
Renal arterial variations (n = 160) (number of subjects)
<2 3–5 6–10 10–20 >20
Number of renal arteries 1 2 3 >3
2 arteries 17 8 8 6 3 42 1–43
Left donated 113 40 6 1 3 arteries 0 1 2 1 0 4 1–35
54 20 3 0 >3 arteries 0 0 1 0 0 1 9–27
Right donated 111 42 6 1
3 0 0 0 †Between the most superior and inferior renal arteries when> 2 ves-
sels present.
Table 3. Distance between the renal arteries when multiple – Right systems were used for kidney donation. In two patients
with partial duplex systems, the contralateral kidney was
RIGHT Kidney: 2 or more renal arteries, n = 49
used for donation.
Total Distance (mm)† Total Range (mm)
(a) (b)
Fig. 3. The 34-year-old female prospective
renal donor. 3D volume-rendered CT demon-
strating a 6mm aneurysm of an upper pole
branch of the right renal artery.
however, they used digital subtraction angiography, Potential living donors are assessed by a multidisci-
which is the gold standard. CT angiography can underes- plinary team that includes nephrologists, transplant sur-
timate the incidence of FMD particularly in the mid and geons, immunologists, radiologists, social workers and
distal renal artery in mild disease. psychiatrists (if indicated). All donors are evaluated with
Renal artery aneurysms (RAA) incidence on CT is serological, urine and radiologic investigations. Many of
reported at approximately 0.7%.21 Accepted indications the investigations and clinical assessments are combined
for treatment of RAA include the following: size> 2 cm, to occur on a single day to reduce the number of visits
medially resistant hypertension, presence in females of that a potential donor needs to make to the transplant
child bearing age, thromboembolism, dissection and rup- centre. Imaging modalities include chest radiography,
ture.22 RAA were identified in 1.9% of our cohort. None abdominal ultrasonography and radioisotope renography
of these met the criteria for intervention. None of these to estimate glomerular filtration rate. Commonly MDCT is
kidneys were used for donation. When present and crite- performed on the same visit. Thus, if a potential donor
ria for treatment have been met, RAA can be treated sur- has been deemed unsuitable for reasons other than
gically with auto-transplantation. More recently, novel anatomical reasons, such as medical and immunological
endovascular techniques have been used with increasing reasons, or due to subject decision not to proceed and/or
frequency.23 change in the health of the potential recipient, they may
Ostial atherosclerosis can make cross-clamping of a have already undergone MDCT. 80 of our screened sub-
renal artery more difficult, and this was present in 3.1% jects (50%) proceeded to donation.
of our cohort (n = 5). When calcified ostial disease is The present study has several limitations. It is a sin-
present, our transplant surgeons do not typically use gle-centre retrospective experience of potential donors
that kidney for donation, even if the no associated in a living-donor programme. Immediate and delayed
stenosis is present. None of the five subjects in our complications in recipients have not been analysed. Ini-
cohort with ostial calcified disease proceeded to dona- tially, this study was conceived as an assessment of
tion. The presence of bilateral renal arterial calcification potential donors and therefore IRB approval had not
is a criterion for exclusion from donation.24 However, granted for evaluation of recipients. This would be a
the identification of atherosclerotic calcification in a relevant outcome measure for success in a living-donor
small vessel can be challenging and is likely underre- programme and should be the aim of further studies.
ported in our cohort. The presence of distal atheroscle- In conclusion, MDCT can identify the significant varia-
rosis is less of an issue from a technical point of view tion in renal arterial, venous and ureteric anatomy. This
however may indicate early vascular disease in that kid- information is crucial for the transplant surgeon.
ney. None of our cohort with mid/distal vessel
atherosclerosis underwent further imaging investigations
based on the MDCT findings. Further investigation with
Acknowledgements
magnetic resonance angiography (MRA) would be per- The authors would like to acknowledge the assistance
formed if a stenosis of> 30% is identified or in the pres- of the transplant co-ordinator team in Beaumont Hospi-
ence of hypertension. tal. The study was discussed at out IRB board and
Ureteric abnormalities are of importance when select- subsequently registered and approved (CA271). All
ing a kidney for transplant, as the ureters will typically authors have approved the manuscript and consent for
need to be anastomosed to the urinary bladder. A duplex publication. This study received no funding. Authors’
system is found in 0.7–3% of the adult population.25 Our contributions are as follows: BM, EC, LT and DON col-
cohort displayed a 3.8% incidence (n = 6) of ureteric lected the data. DON, ML, RD and MM prepared the
abnormalities, complete duplex systems in 2 cases. Two manuscript. DON, DL and MM conceptualised and
case in our cohort with partial duplex systems proceeded designed the study. DON, MM, LT, BM and EC analysed
to transplant. the data.