Pelvic Nerve Neuropathy After Kidney Transplantation
M. Nikoobakht, A. Mahboobi, A. Saraji, A. Mehrsai, A. Emamzadeh, M.T. Mahmoudi, and G. Pourmand
ABSTRACT
Objectives. We examined the relation of various age, gender, diabetes, hypertension,
and graft function with the prevalence of femoral and lateral cutaneous nerves sensory
and/or motor disturbances after kidney transplantation.
Materials and Methods. Among 129 patients who underwent kidney transplantation
from April 2001 to March 2002. We excluded, 10 due to preoperative sensory disturbances.
We evaluated the prevalence of sensory and/or motor disturbances preoperatively by
physical examination and postoperatively by both physical and electromyography examinations. The cinical findings were correlated with the following risk factors: age, gender,
preoperative dialysis duration, background diseases. (e.g., diabetes, hypertension), graft
weight, nephron mass index, operative and retraction time, and rejection episodes.
Results. At 1 to 9 days postoperatively, 31 ng (26%) patients, suffered neuropathy of the
lateral cutaneous nerve and 4 (3.3%), femoral neuropathy. No meaningful relation was
detected between the incidence of neuropathy and these risk factors. The probability of
neuropathy was greater among diabetics, hypertensives, women, and those with graft
rejection episodes. All of these complaints were temporary.
Conclusions. Post-kidney transplant femoral and/or lateral cutaneous nerve neuropathy
is a prevalent complication particularly in diabetic, hypertensive, and female patients.
Neuropathy is also more evident after graft rejection.
S
ENSORY (and/or motor) disturbances in the thigh
after kidney transplantation is a relatively prevalent
complaint.1 Kidney transplantation improves life quality
among patients suffering end-stage renal disease. Still, some
problems may occur after kidney transplantation that influence the life quality, presently an important facet of disease
treatment. The lateral cutaneous nerve of the thigh (LCNT)
originates from the roots of L2 and L3 progressing through
the lateral anterior thigh from the inguinal ligament to the
knee. Slight numbness, tenderness, and sometimes pain
may occur when it is damaged. Touch and needle perception are decreased.2
The femoral Nerve (FN) includes nervous roots of L2, L3
and L4. It has two sensory and motor parts. It expands
through the pectineous, sartorius, and quardriceps muscles
and mediates inner anterior surface sensation in the thigh
and foreleg. Damage causes hyposthesia, paresthesia, pain
in the anterior and inside thigh and foreleg, together with a
feeling of weakness when the knee is bent.2 This prospective study sought to describe the prevalence of these side
effects and study the probable risk factors.
MATERIALS AND METHODS
Among 129 kidney transplants from April 5, 2002, to March 19,
2003, we excluded 10 patients who showed cerebral apoplexy,
before thigh neuropathy or sensory disturbance. Patients underwent neurologic investigations 1 day before as well as 1 day and 1
week after transplant, including description and physical examination for the LCNT and FN. The lateral and anterior thigh power
hip flexion and knee extension as well as knee reflexes. Whenever
the clinical evaluation was positive, suggesting confirmation of the
diagnosis, as well as electromyography, and nerve conduction
velocity studies were performed during the second week. We
recorded age (in years), gender, dialysis time (in months), diabetes
record, hypertension record, height (in meters), weight (in kg),
anastomotic time (time necessary from the beginning of anastomosis up to removal of clamp), retractor time (from placement to
removal of retractor), operation time (from the beginning of
From the Urology Research Center, Tehran University of
Medical Sciences, Tehran, Iran.
Address reprint requests to M. Nikoobakht, Urology Research
Center, Sina Hospital, Hasan Abad SQ, Tehran, Iran. E-mail:
nikoobakht_m@hotmail.com
0041-1345/07/$–see front matter
doi:10.1016/j.transproceed.2007.03.085
© 2007 by Elsevier Inc. All rights reserved.
360 Park Avenue South, New York, NY 10010-1710
1108
Transplantation Proceedings, 39, 1108 –1110 (2007)
PELVIC NERVE NEUROPATHY
1109
incision up to complete skin suture in minutes) and transplanted
kidney weight. Plasma creatinine level on the third day after
operation together with that at discharge (in mg/dL) and episodes
of rejection were recorded. During the first week after transplantation, ultrasonography of kidney was performed to evaluate the
existence or not of a collection around the kidney. The calculation
method for the nephron mass index was as follows: weight of
transplanted kidney(g)/BMI and BMI was calculated as: (kg)
wigth/(m*m) height. Logistic regression analysis was used for data
analysis.
RESULTS
Mean patient age was 40.45 years. The 119 patients included 80 men and 39 women. From among 119 patients, 35
were suffering from neuropathy (29.4%), 31 of which were
related to LCNT (26.05%), and 4 to FN (3.36%). Among
patients suffering from femoral neuropathy, paresis was
observed in 100% of patients, but none was affected by
paralysis. Pain, paresthesia, and hypesthesia were observed
in 100%, 50%, and 100% of patients, respectively. Considering neuropathy of the LCNT nerve, pain with irritation
was observed among 22.58% with paresthesis and hypesthesia in 74.19% and 96.77% respectively. The scope of
time to appearance was 1 to 9 days, the median of which
was 1 day and mean, 1.6 days. Risk factors were not
statistically analyzed among patients suffering from the
femoral disorder due to the small number of persons
affected. But diabetes was not seen among these patients;
25% had rejection and 50%, hypertension. Neuropathy of
the thigh and LCNT neuropathy is shown in Tables 1 and 2.
No variable increased neuropathy meaningfully, but in
special cases, these were interacting odds ratios. Increased
Table 1. Sensory Disturbance in the Thigh After Renal
Transplantation Evaluating Possible Predisposing Factors
Variable
P Value
Odds
Ratio
95% Confidence
Interval
Age
Gender
Duration of dialysis
Height
Weight
Diabetes
Hypertension
Deaver time
Anastomtic time
Warm ischemia
Cold ischemia
Local atherosclerosis
Transplanted kidney weight
Nephron mass index
Creatinine day 3
Creatinine at discharge
Antilymphocyte globulin
Rejection
Acute tubular necrosis
Collection volume around
transplanted kidney
.7090
.5127
.6620
.8465
.6305
.2459
.1344
.372
.0891
.1413
.1962
.8041
.6293
.3349
.0118
.1384
.4533
.4175
.1662
.3483
.994
.709
.996
1.534
.993
1.966
1.467
.989
.963
.816
.977
.889
1.003
1.108
1.050
.202
.72
1.471
.398
.998
.961–1.27
.332–1.735
.978–1.0114
.020–116.885
.965–1.022
.628–6.157
.663–3.247
.965–1.013
.921–1.006
.623–1.07
.644–1.012
.350–2.255
.990–1.017
.900–1.364
.907–1.216
.942–1.532
.305–1.699
.579–3.741
.108–1.466
.994–1.002
Table 2. Neuropathy of Lateral Cutaneous Nerve of the Thigh:
Evaluating Possible Predisposing Factors
Variable
P Value
Odds
Ratio
95% Confidence
Interval
Age
Gender
Duration of dialysis
Height
Weight
Diabetes
Hypertension
Deaver time
Anastomtic time
Warm ischemia
Cold ischemia
Local atherosclerosis
Transplanted kidney
weight
Nephron mass index
Creatinine day 3
Creatinine at discharge
Antilymphocyte globulin
Rejection
Acute tubular necrosis
Collecetion volume
around transplanted
kidney
.4469
.6446
.5269
.917
.3130
.1605
.3217
.1803
.0771
.1054
.1142
.9292
.9273
.986
.815
.994
1.274
.984
2.28
1.523
.983
.966
.789
.972
1.044
1.001
.952–1.022
.342–1.942
.976–1.013
.013–121.549
.955–1.015
.721–7.207
.663–3.500
.958–1.008
.919–1.004
.591–1.051
.938–1.007
.406–2.682
.987–1.015
.2547
.6586
.1809
.730
.4303
.239
.4300
1.13
1.034
1.177
.857
1.478
.455
1.007
.913–1.412
.892–1.199
.927–1.495
.357–2.057
.560–3.906
1.123–1.686
.989–.026
age did not increase neuropathy risk. Neuropathy was 1.32
times more prevalent in women. Dialysis time, weight, and
height had no effect on appearance of these side effects.
Times of anastomosis and retractor do not increase the risk.
Diabetes added 1.96 times and hypertension 1.46 times to
the risk. The weight of the transplanted kidney showed no
effect on the occurrence of neuropathy.
Nephron mass index had no effect. Rejection added 1.47
times to the risk and creatinine at discharge added 1.2 fold.
However, none of these factors was significant.
DISCUSSION
Neurologic complications are frequent among renal transplant recipients and may contribute to morbidity. Acute
femoral neuropathy may occur in about 2% of patients as a
result of nerve compression after the operation.1 It also may
be due to the uremic state of renal failure.2 For this reason,
we excluded 10 patients who had sensory disturbances in
the thigh before transplantation. According to our study,
the rate of sensory disturbance of the femoral nerve was
29.4% of which 26.05% were related to the LCNT and
3.36% to the FN. Certain mechanisms have been proposed
for complete FN palsy or ischemia, such as clamping the
internal iliac artery or steal phenomenon.3 There may be
direct surgical damage to the vessels supplying the femoral
nerve4 or direct compression of the femoral nerve by the
transplanted kidney, by a self-retractor or by a hematoma.6,7
Vaziri et al8 demonstrated compression of the FN retaining
by the medial and inferior blade of self-retaining retractors
during renal transplantation as the cause of femoral neu-
1110
ropathy after renal transplantation; in our study, retractor
time was not increased. Other studies about diabetes and
neuropathy have suggested that it is a risk factor for
postoperative sensory disturbances of the thigh.3,5 After
excluding diabetic patients with preexistent neuropathy,
diabetes was shown to increase the probability of LCNT
neuropathy 2.28 times and thigh neuropathy 1.96 times,
although these values were not significant. Diabetes may
predispose to this side effect. Larger studies should be
performed. Uremia has been proposed to be an important
factor,4 but the present study failed to reveal a meaningful
relation between disease time, dialysis time, and neuropathy.
In patient with acute rejection, neuropathy in the thigh
was 1.47 times higher. Immunologic mechanisms or increased lymphatic flow may be responsible. Creatinine at
discharge BMI, and nephron mass index did not show
significant relations with this side effect. Weight of the
kidney had no effect. Hypertension and female gender
increased femoral neuropathy risk by 1.47 and 1.32, respectively.
NIKOOBAKHT, MAHBOOBI, SARAJI ET AL
In conclusion, the incidence of femoral neuropathy after
renal transplantation was 3.36 in our study with increased
incidence among women, diabetics, and hypertensives.9
REFERENCES
1. Murata Y, Sakamoto K, Hayashi R, et al: Sensory disturbance
of the thigh after renal transplantation. J Urol 165:770, 2001
2. Ropper AH, Brown RH: Adams and Victor’s Principles of
Neurology, 8th ed. New York: McGraw Hill; 2005, p. 271
3. Jog MS, Turely JE, Berry H: Femoral neuropathy in renal
transplantation. Can J Neurol Med Sci 21:38, 1994
4. Yasbeck S, Larbrissen A, O’Regan S: Femoral neuropathy
after renal transplantation. J Urol 134:720, 1985
5. Sharma KR, Cross J, Santiago F, et al: Incidence of acute
femoral neuropathy. Arch Neurol 59:541, 2002
6. Sisto D, Chin WS, Geelhoed GW, et al: Femoral neuropathy
after renal transplantation. South Med J 73:1464, 1980
7. Meech PR: Femoral neuropathy following renal transplantation. Aust NZ J Surg 60:117, 1990
8. Vaziri ND, Barton CH, Ravikumar GR, et al: Femoral
neuropathy: a complication of renal transplantation. Nephron
28:30, 1981
9. Vaziri ND, Barnes J, Khosrow M, et al: Compression neuropathy subsequent to renal transplantation. Urology 7:145, 1976