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Nerve Sparing Robotic Prostatectomy:
A Novel and Minimally Invasive Treatment of Prostate Cancer
PCRI
Insights November 2004 vol. 7, no. 4
See update in November 2007 Insights
By Ashutosh Tewari, MD, Director Robotic Oncology and
Prostate Cancer Outcomes at Weill Cornell Medical School, New York
Presbyterian Hospital, and Mani Menon, MD, Director of Vattikuti
Institute of Urology, Henry Ford Hospital, Detroit, MI
Supported by: Akshay Bhandari, MD, Sanjeev Kaul, MD, James
Peabody, MD, Alok
Shrivastava, MD, Ashok Hemal, MD, Melissa Fisher,
MD and Kurshid Guru, MD
Introduction
Recent developments in the field of
surgical robotics have ushered in a
new era of minimally invasive surgery
that now challenges conventional
open surgery. Currently available telemanipulation devices allow the performance of
complex surgical tasks with dexterity and minimal
fatigue due to their ergonomic design,
expanded degree of movements, tremor filtering,
and 3-D stereoscopic visualization. These
devices provide an unsurpassable view of the
operative field and unrestricted ability to execute
any surgical task. Robotic surgery has been
embraced by urologists who have applied it to
complex surgical procedures such as pyeloplasty,
radical cystectomy, donor nephrectomy, and
radical prostatectomy.
Background
Goals of treatment. The goal of treating
prostate cancer includes complete eradication of
cancer coupled with minimal morbidity and
negligible deterioration of quality of life. In order
to meet these goals, we use a da Vinci master-slave
robot system and have developed a minimally
invasive, robot-assisted radical prostatectomy
technique. This is accomplished (1) by
standardizing a unique sequence of surgical
steps, appropriate visual angles using different
lenses, optimal retraction strategies, precise
suturing steps, and anatomical sparing of the
neurovascular structures
and (2) by incorporating time-tested open surgical principles. This
technique (which we call the VIP technique)
results in excellent oncological and surgical outcomes;
causes minimal bleeding, and can be
completed in 90 to 160 minutes. The patient satisfaction
has been tremendous. Not only do both
patients and families appreciate the cosmetic
benefits, but also hospitalization has been significantly
reduced. Most patients can revert back to
their normal lifestyle in less than two weeks.
Dr. Menon developed the
technique in Detroit at the Vattikuti Institute of Urology and
it has been popularized at several centers in the
USA. The data presented here is based on published
data from Henry Ford Hospital.
Patient selection. Men with clinically
localized prostate cancer who choose surgical
treatment are candidates for this procedure.
The authors use survival prediction tables for
selecting patients for surgical treatment. The
data has been published by the authors
and is available online at: www.prostatecalculator.org/survival.html.
Patients
undergo a thorough preoperative evaluation including serum PSA testing,
an
international prostate symptom score (IPSS),
a sexual function inventory, a quality of life
score, and an incontinence questionnaire.
We also record information about other co-morbidities,
such as stroke, cerebral aneurysm, diabetes
mellitus, hypertension, COPD (chronic
obstructive pulmonary disease) and history of
myocardial infarctions.
We specifically question each patient regarding
his medical history, with emphasis on
abdominal surgery, peritonitis, knee or hip
surgery, or peripheral neuropathy. Previous
abdominal surgery is not a contraindication.
However, a history of stroke or cerebral aneurysm
is a relative contraindication for this procedure,
since, for 1-3 hours, the patient would be placed
in a pronounced Trendelenberg position, in
which he is placed head down on a table
inclined at about 45° from the floor with the
knees uppermost and the legs hanging over the
end of the table.
Patients are admitted on the day of surgery
and receive deep vein thrombosis (DVT) prophylaxis (Heparin 5000 IU SC on call to the operating
room) and an antibiotic in the preoperative
holding. Venodyne boots, which gently compress
the patient’s legs during surgery to prevent postoperative
embolic problems, are placed and the
abdomen is shaved from nipple to groin.
Brief Overview of Operative
Technique
Da Vinci robotic technology (Figures 1, 2
and 3). The da Vinci system uses a sophisticated
master-slave robot that incorporates 3-D
visualization, scaling of movement and wristed
instrumentation. The system has three multijoint
robotic arms with one controlling a binocular
endoscope and the other two controlling
articulated instruments.


Two lenses, 0° and 30º,
are used. Two finger-controlled handles (the
“masters”) that are housed in a mobile console
are used to control the two robotic arms and,
together with a foot pedal control, also control
camera movement. Instrument movement can
be scaled from 1:1, which allows exact finger
movements to be transmitted to the instrument
tip, to 1:3 and 1:5, which scale down the movements
to allow precise and delicate dissection.

The stereoscopic three-dimensional
vision allows magnified (10-15-fold) vision with
depth perception. This visual advantage
improves tissue delineation and precise dissection
of delicate neurovascular tissue.
Surgical Team. The robotic team includes
both console-side and patient-side surgeons
(Figure 4). The operating surgeon sits at the
console, and is not scrubbed. After the patient-side
team is scrubbed, they place the ports, present
the operative field to the operating surgeon,
and use suction to keep the field clean.
Surgical Steps. Armed with the findings
of anatomic studies, we developed
our Veil of Aphrodite technique for nerve-sparing. The
details of robotic prostatectomy technique
have been described previously elsewhere.
We first incise the peritoneum over the bladder
(Figure 5).

The prostatic veins are secured
with a stitch, and the junction between
prostate and bladder is dissected precisely. We
control the prostatic arteries (pedicles) by
clips, by sutures, or occasionally by individually
coagulating the vessels with a bipolar forceps.
The anatomic location of the nerves are
previously described (Figure 6).

These nerves are precisely dissected and left in the patient for
future
erectile function (Figure 7).

The lymph nodes are removed
as would be
done in any open procedure. The opening in
the bladder is sutured to the end of the urethra to re- create the continuity. The endo wrist technology and magnified
3-D
vision maximizes precision and allows anastomosis (suturing) to be
more secure and watertight.
We try to avoid damaging the muscles surrounding
the urethra and thus leave the sphincter intact. This enables early
return of urinary
control.
We also preserve maximum blood supply to the urethra and other surrounding
structures by precisely suturing only those vessels that are entering
the prostate and are absolutely required for the safe removal of the
cancerous
gland. We attempt to identify any local spread by use of frozen sections
and take counter measures to maximize cancer control.
Retrieval of specimen
and completion of surgery. The cancer containing prostate
gland is entrapped (intact) in a thick plastic bag to
avoid any tumor spillage. We remove the specimen after slightly enlarging
the umbilical incision as required, and we use plastic steri-strips
for surgical
closure of the incisions.
Postoperative care and discharge. The patients
are sent to recovery on intravenous fluids, antibiotics and pain meds.
They usually are
walking on the evening of the operation and go home either on the same
day or
the
next morning. The catheter is removed between 4-7 days after surgery.
It is
rare to use blood transfusions in this procedure, and the post-operative
pain
is minimal. Patients have small cosmetic incisions, and they go back
to
their work in approximately 12-14 days. Many patients, who are from
distant places fly back to their homes in 1-2 days.
Contemporary Results
From a patient perspective, the following concerns have
been reported to
have the most influence on prostate cancer therapy: oncological control
(margin and PSA recurrence), pain, complications, convenience (catheter duration
and hospital stay) and functional outcomes (incontinence and sexual
recovery). Herein, we analyze the results of our published series
of
patients treated with robotic prostatectomy in comparison with open
radical retropubic
prostatectomy (RRP), bearing in mind the aforementioned
patients’ key preference points. The following discussion is
based on this
work. Table 1 shows that the baseline patients’ characteristics
in both
groups were comparable.

Cancer Control. As shown in Table 2, the oncological
results are compared in two groups – 100 RRP patients and 200
robotic patients. The surgical specimen was inked and processed for
histo-pathological analysis. Margins were considered positive if there was a tumor present
at the ink. For the apex, margins were considered positive if the margins
of the apical biopsies, which represent the actual margin of the apical
dissection, had cancer.

The Gleason scores and
pathological stages were comparable between two groups. Twenty-three
percent of the RRP patients had a
tumor at the inked margin. In the robotic prostatectomy group, we performed
intra-operative biopsies to excise additional peri-apical
collar of
the distal tissue. The residual positive tumor was seen only in 9%
of the
cases. A total of 85% of the RRP patients and 92% of the robotic prostatectomy
patients had an undetectable PSA at a mean follow-up of 556
and 236 days respectively (p<0.05).
Pain. As seen in Table 2, the
robotic prostatectomy patients had much less post-operative pain, which
was managed predominantly with oral
Cox 2 inhibitors such as Celebrex.®
Inconvenience. Mean hospitalization
stay and duration of catheterization were significantly shorter for
the robotic prostatectomy group (See
Table 2). Therefore the inconvenience of staying in the hospital
and the length
of
time until catheter removal were less with robotic prostatectomy
procedure.
Risks and Complications. As shown in Table 3, robotic prostatectomy
is quite safe and the minor and major complications were one-fourth
those experienced by the patients undergoing open radical prostatectomy.

Nerve-Sparing Results. We have developed
some modifications in nerve-sparing that
utilizes the benefits of robotic technology. In
particular, we have improved three-dimensional
stereoscopic vision and intuitive multidirectional
movement of miniaturized robotic
instruments. The foundations of nerve-sparing
have been based on Walsh’s initial principles
and later data from cadaver dissections. These
studies elucidated the course of nerves as seen in
Figures 6, 8, and 9. We delicately dissect the
nerves using (1) micro scissors and (2) delicate
control of bleeders. The incidence of patient reported
sexual functions is quite encouraging.
We have also made technical modifications
for improved continence as well as sexual function.
The anatomy of the sphincter complex is clearly
visualized, and we attempt to minimize
dissection in the vicinity of continence muscles
and preserve its nerve and blood supply.

Continence. Based on third
party telephone interviews, we used survival analysis to compute
the probability of return of continence by two
groups of the patients. Robotic prostatectomy
patients achieved continence much more
quickly than RRP patients; achieving a 50%
return of continence required 160 days in RRP
arm as opposed to 44 days in robotic
prostatectomy patients (p<0.05).
Sexual Function. The sexual function was also
evaluated using third party telephone interviews. The response
was compiled as the ability to (1) achieve erections and (2) maintain
erections
adequate for intercourse. The analysis was limited
to (1) patients who classified themselves as
having normal preoperative erections and sexual
intercourse and (2) the ones who underwent
bilateral nerve sparing. The response indicated
that robotic prostatectomy patients’ erections
returned more than twice as quickly [50% return
of erection occurred at mean follow-up of 180
days vs. 440 days for RRP patients (p<0.05)]. The return
of intercourse was also quicker in the robotic prostatectomy group
in which 50%
patients achieved intercourse at a mean follow-up
of 340 days. Conversely, the RRP patients have
not yet achieved 50% return of intercourse at 700
days (p<0.05). Forty two percent of robotic
prostatectomy and 65% of RRP patients were
known to be using Sildenafil (Viagra®) at the
time of analysis.
Operative Comparisons. The robotic
prostatectomy patients needed an extra 15 minutes
for the setup, but the overall operative times
were comparable in two groups. On the other
hand, the blood loss of the robotic prostatectomy
patients was one-tenth that of the RRP patients.
Using this technique, a trained robotic team
can perform 3-6 cases a day.
Robotic versus Laparoscopic Prostatectomy
In laparoscopy, the surgeon uses long instruments
through small openings and maneuvers
them with direct hand contact. Robotic systems
use even more delicate instruments that possess
two additional degrees of movement
excursion (for a total of six, as with a human
hand). Comfortably seated at the robot console,
the surgeon can maneuver the instruments
via a computer interface.
Laparoscopic radical prostatectomy is associated
with a steep learning curve. Even in the
hands of expert surgeons, laparoscopic radical
prostatectomy requires extensive learning;
approximately 40 cases are needed to master this
technique. In contrast, the learning of robotic
prostatectomy seems to be more intuitive and
less demanding. Wood and Woolf compared 10
robotic prostatectomies with 10 laparoscopic
prostatectomies, all performed by the same surgeon,
who is an experienced upper urinary tract
laparoscopist. Despite this surgeon’s
large amount of laparoscopic experience, the mean
operative time was on average 145 minutes less
for robotic than for laparoscopic prostatectomy.
The estimated blood
loss was comparable (<
500 cc), and there were two conversions (to RRP) in each
group, but no major complications occurred.
The authors’ group performed
48 laparoscopic radical prostatectomies and 50 robot-assisted
prostatectomies within a 12-month period. The
preoperative and intraoperative demographical
variables were comparable in both groups as
were the operative times, changes in
hemoglobin concentrations, durations of hospitalization,
positive margin rates, and overall
complication rates. All measured clinical and
pathologic parameters were comparable to the
best laparoscopic radical prostatectomy results
reported in the literature.
Conclusions
Robotic prostatectomy is a safe, effective and
reproducible technique for removing the
prostate. In most patients, it can be performed
within one and a half to two hours with minimal
blood loss and few complications. The procedure
incorporates principles of both laparoscopic and
open radical prostatectomy. The patients enjoy
benefits of surgical treatment in the setting of
less invasion, minimal pain, limited blood loss
and early functional and overall recovery.
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