Surgical Procedure
Use of a New Nerve Stimulator During
Radical Prostatectomy
David T. Chang, MD
Postdoctoral Residency Fellow
Senior Resident
College of Physicians and Surgeons
Columbia University
New York, New York |
Erik T. Golubuff, MD
Director of Urology
Allen Pavilion
Columbia-Presbyterian
Medical Center
New York, New York |
Carl A. Ollson, MD
John K. Lattimer
Professor & Chairman
Squier Urological Clinic
Medical Center
New York, New York |
Prostate
Cancer is the most commonly diagnosed visceral malignancy in men in the United States. In 1998, estimates indicated that 184,500 new
cases of prostate cancer would have been diagnosed and that approximately 39,200 men would
die from the disease by the end of the year. One
of the more common treatments for the localized prostate cancer involves surgical
extirpation of the prostate during radical prostatectomy.
Although this surgical procedure offers some survival advantage with long term
follow-up, the occurrence of complications such as incontinence and erectile dysfunction
has prompted concern in both patients and physicians.
To address this
issue, Walsh and colleagues initially studied the preservation of the postoperative
erectile function by defining the usual location of the cavernous nerves in terms of their
relation to prostate and urethra (Figures 1A and 1B).
Using this knowledge, Walsh developed and described the anatomic radical retropubic
prostatectomy, a procedure specifically designed to preserve the cavernous nerves while
still allowing surgical extirpation of the cancerous prostate.
Background
The appeal of the anatomic approach to radical
prostatectomy results from the preservation of the cavernous nerves and their stimulatory
signals to the penis. Reported rates of potency following radical prostatectomy range
widely from 11% to 86%, however. This
variation may result from a number of factors, including differences in surgical
technique, discrepancies in preoperative erectile status, age variation within study
populations, and variation in the methods used to determine
postoperative potency.
In general,
success rates are reportedly higher in studies from larger university centers when
compared with general Medicare population. In
addition, complete return of erectile function to preoperative levels is less likely in
patients who are older and have more advanced disease.
The number of
neurovascular bundles preserved during radical prostatectomy is another factor that
appears to correlate with postoperative erectile status.
Specifically, higher rates of potency are generally associated with bilateral nerve
preservation compared with the unilateral preservation of bilateral nerve sacrifice. Therefore, newer techniques that refine the
anatomic nerve-sparing radical prostatectomy would theoretically improve
postoperative quality of life for many patients.
In particular,
more accurate intraoperative identification of the neurovascular bundles may be helpful. Even well intentioned attempts to preserve the
neurovascular bundles and cavernous nerves are sometimes unsuccessful because locating
these structures proves difficult. This
problem may result from variation in the location of the neurovascular bundles; presence
of blood in the operative field, which makes visualization of the bundles difficult; or
even poor exposure due to body habitus.
A recently
developed device helps urologic surgeons identify and map the neurovascular bundles so
they may attempt to improve postoperative potency. Patient
selection for use of this surgical apparatus follows conventional criteria for radical
retropubic prostatectomy with localized prostate cancer.
Equipment
The new device, called CaverMap
Surgical Aid (Blue Torch Corporation, Norwood, Mass), combines a nerve stimulator with an
erectile response detection system for intraoperative use.
This system consists of three major components (Figure 2). The control unit contains the digital and analog
electronics, adjustable controls, user interface, and connectors for the probe handle and
disposable kit. The probe handle, which is
sterile and reusable, is the component that allows the surgeon to control the device
intraoperatively. The disposable kit, which
contains items for onetime use, is made up of the probe tip that attaches to the probe
handle, the tumescence sensor, and the lead that connects the sensor to the control unit. The electrode containing probe tip emits the
electrical current.
General Use
The probe tip is placed on tissues that
are suspected to contain sensitive nerves. When
the tissue is stimulated, erectile responses are detected in the form of minute changes in
penile circumference in a previously placed tumescence sensor. A full erection is not achieved for two reasons: (1) only external nerve stimulation is used, (2)
other coordinated signals and changes in vasculature are usually required for a normal
erection. Rather, a small erectile response
in the form of an increase or decrease in penile girth is produced.
Based on the
presence or absence of a confirmed response, the course of the cavernous nerves can then
be mapped, and informed decisions regarding the dissection pattern to be used can be made
for each individual patient. The CaverMap
Surgical Aid can also be used to assess the functional state of the cavernous nerves at
the end of the procedure.
Stimulation is
accomplished by inducing a biphasic current pulse train for up to 80 seconds with a
controlled current intensity (8 to 20 mA) and pulse duration of 800 microseconds. The device is programmed to provide a gradual
increase in current (from 8 to 20 mA) in 20-second increments.
Changes in
penile circumference are electronically detected and displayed as relative change, with
both visible and audible di splays (light-emitting diode [LED] scale and changes in a tone,
respectively). The penile sensor contains a
small amount of mercury that allows measurement of electric resistance to the supplied
current. As the penile circumference changes,
so does the length of mercury in the sensor loop, which is reflected in minute changes in
resistance. Minimal changes in tumescence of
0.5% are considered positive responses to nerve stimulation. To avoid exhausting the erectile response,
stimulation is discontinued once an unequivocal response is reached, with no attempt to
determine maximal responses with higher current intensity.
Operative Technique
Step 1: Anesthesia and preliminary dissection
After prophylactic antibiotics are
given and sequential intermittent compression devices are placed and activated,
endotracheal anesthesia is administered. The
patient is prepped and draped according to surgeon preference. Prior to placement of the initial Foley catheter,
the tumescence sensor is placed around the base of the penis (Figure 3). The sensor, a thin, elastic, circular piece,
should fit snugly around the base of the penis. This
strain gauge is connected to the control unit so that the system is able to sense changes
in penile diameter in response to nerve stimulation.
A lower midline
incision is used to enter the space of Retzius, and appropriate retraction is placed for
adequate surgical exposure. Following
bilateral pelvic lymphadenectomy (with or without pathologic analysis of frozen sections),
the periprostatic fat is removed and the superficial brand of the dorsal vein is divided. The puboprostatic ligaments are divided or
preserved according to surgeon preference, and the endopelvic fascia is incised.
Step 2: Determining baseline nerve status and function
Baseline responses to nerve stimulation
should be established either at this time or foll owing
division of the dorsal vein complex and urethra. The
CaverMap Surgical Aid is used to stimulate the neurovascular bundles bilaterally as they
pass through the tissue posterolateral to the urethra (Figure 4). The probe tip may be bent to various angles to
facilitate placement into the desired position along the prostate. If no tumescence response is obtained, the
stimulation procedure is discontinued, and the procedure proceeds as the surgeon would
ordinarily. If a response is obtained,
further stimulation is then performed.
Step 3: Mapping neurovascular bundles
Stimulation
proceeds sequentially along the lateral aspect of the prostate at the prostatic apex, the
mid region, and the base of the prostate. By
noting where the probe tip is located when it elicits a tumescence response, the course of
the neurovascular bundles becomes apparent and provides an anatomic map for
the surgeon interested in their preservation.
The degree of
stimulation is controlled by the probe handle, which has both coarse and
fine switches (Figure 5). When
the coarse switch is activated, the signal is delivered along eight electrodes
across the tip to locate the general vicinity of the neurovascular bundles. When the fine switch is activated, the
output is changed so that the stimulatory signal is delivered along only four, two, or one
electrode(s) at the probe tip for more precise, accurate localization of the neurovascular
bundles.
Step 4: Dividing the lateral pedicle
Beginning at
the apex of the prostate, the lateral attachments are divided and controlled according to
surgeon preference. If a tumescence response
is noted when stimulating tissue, that tissue
is spared. The lateral tissues are mobilized
closer to the prostate, and special attention should be paid to the remaining
extracapsular tissue during this dissection. This
should not be preserved at the expense of transecting the prostatic capsule or a palpable
neoplasm. In that case, the neurovascular
bundle should be sacrificed and included with the specimen to perform the proper cancer
operation.
Stimulation
is then performed sequentially in cephalad direction.
The coarse and fine switches may be used for precise
localization of neurovascular bundles. If
stimulation produces a tumescence response, tissue is preserved; this tissue overlies the
neurovascular bundles. Dissection continues
in a cephalad direction to the level of the bladder neck.
Step 5: Completing the procedure
Following
complete removal of the prostate and seminal vesicles with ligation of the vasa
deferentia, hemostatis is achieved, and the bladder neck is reconstructed according to the
surgeon preference with eversion of the bladder mucosa.
Before vesicourethral anastomosis is performed, the CaverMap Surgical Aid can be
used to stimulate the neurovascular bundles once more to confirm unilateral or bilateral
nerve function. The anastomosis is then
completed, a final Foley catheter and drains are placed, and the wound is closed in
layers.
Clinical Experience
Initial
clinical experience with the CaverMap Surgical Aid appears promising. In the first published study to examine the
clinical usefulness of this device, Klotz and Herschorn reported a 84% success rate
preserving erectile function in 17 patients who underwent intraoperative dissection guided
by the nerve stimulator. However, on a more
cautionary note, these investigators also reported a 12% rate of positive margins at
either the apical or lateral regions. Whether
this might have been prevented without using the CaverMap Surgical Aid is not known.
Our
clinical experience with the CaverMap Surgical Aid so far has been positive. The easy-to-use device is now in routine use at
our institution for those patients who undergo radical retropubic prostatectomy and who are also candidates for nerve-sparing
procedures.
Summary and Conclusions
Erectile dysfunction following radical
prostatectomy results from a number of factors, and preservation of the neurovascular
bundles contributes to better postoperative potency.
The CaverMap Surgical Aid uses a nerve stimulation device to identify and map the
route of the neurovascular bundles and the cavernous nerves during radical prostatectomy. This information allows the surgeon to perform the
nerve-sparing prostatectomy with improved results, particularly in cases where the anatomy
may not be obvious.
This technology
must be used judiciously. Although it
provides much more anatomic information that ever before, the surgeon must balance the
sometimes incompatible goals of a negative margin of resection with preservation of the
neurovascular bundles. No direct evidence
suggests that the CaverMap Surgical Aid contributes in any way to increases in the rates
of margin positivity, but knowledge of the precise location of the neurovascular bundles
may increase the temptation to remove a smaller than usual margin. This may occur in an effort to preserve a bundle
that is closely apposed to the prostate and that may have ordinarily been divided during
the dissection.
Another benefit
of using the CaverMap Surgical Aid involves helping establish baseline and postdissection
continuity and determining efficacy of the cavernous nerves. In particular, a tumescence response following
removal of the surgical specimen is reassuring in demonstrating a physical neural
connection between the area receiving stimulation and the penis.
Investigators at our institution and
others are now performing controlled studies with longer periods of follow-up. When the resulting data are available, they will
be stratified and analyzed to determine the true benefit of the CaverMap Surgical Aid. With confirmation of the promising initial
results, cavernous nerve mapping may become a standard part of anatomic radical
prostatectomy.
Suggested Reading:
Hendrick JG, Kaplan SA. What the literature reveals about the
complications of radical retropubic prostatectomy. Contemp
Urol 1997; 1:13-22.
Klotz L, Herschorn
S. Early experience with intraoperative cavernous nerve stimulation with penile tumescence
monitoring to improve nerve sparing during radical prostatectomy. Urology 1998; 52: 537
542.
Quinlan DM, Epstein JI, Carter BS,
et al. Sexual function following radical
prostatectomy: Influence of preservation of neurovascular bundles.
J Urol 1991; 145-998-1002.
Walsh PC. Anatomic radical retropubic prostatectomy. In: Walsh PC, Retick AB, Vaughan ED, et al, eds.
Campbells Urology. Toronto, Ontario: WB Saunders; 1998: 2569-2585
Walsh PC, Lepor H, Eggleston C.
Radical Prostatectomy with preservation of sexual function: Anatomical and pathological
considerations. Prostate 1993: 4:473-485
Copyright ã 1998 by MPI.
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