Quality of Life Clinical Trial
Official title:
Abdominal Midline Incisional Hernia Repair and Functional Outcome: Randomized Controlled Trial to Compare Open and Laparoscopic Surgical
Background: Midline incisional hernia is reported from 0,5 to 11% after abdominal
operations. Primary repair without mesh reinforcement is almost abandoned because of high
recurrence rates (24 to 46%). Use of prosthetic mesh in incisional hernia repair lowered the
recurrence rates under 10%. Recurrence rate alone is not the main quality criterion for
incisional hernia repair anymore. Large series and meta-analyses confirmed the value of
laparoscopic repair as at least equal if not better compared with open repair. Discomfort,
pain, diminished quality of life and body image alteration influences functional well being.
No baseline information exists in any of these fields treating pre- or post-operative phases
in patients with incisional hernia. Respiratory functions and medico-economic evaluation are
other rarely investigated fields that we consider in our trial. The objective of this study
is to analyse the functional outcome status of patients after laparoscopic incisional hernia
repair compared to open repair.
Methods: A randomized controlled non-blinded clinical trial is designed to compare
laparoscopic incisional hernia mesh repair with open repair on post operative pain, health
related quality of life outcomes, body image and cosmetic measurements, respiratory
functions, recurrence rates, and cost. Volunteers will be recruited in Geneva University
Hospital, department of surgery, visceral surgery unit. Eligibility criteria is male patient
aged over 18 years, with reducible incisional hernia who are candidates for elective surgery
and medically fit for general anesthesia.30 patients will be enrolled for each group.
Follow-up will take place at 10th, 30th days as well as 3 12 and 24 post operative months by
questionnaires and by clinical exam by independent expert. An overall cost-analysis will be
realized. Patient enrollment in the study will start in April 2008 and estimated to end in
september 2009.
Midline incisional hernia is reported from 0,5 to 11% after abdominal operations.
Discomfort, pain, body image alteration and diminished quality of life influences functional
well being. Alteration in pulmonary function, risk of visceral incarceration or cutaneous
complications are potential medical complications. Primary repair without mesh reinforcement
is almost abandoned because of high recurrence rates (24 to 46%). Recurrence rate with
prosthetic repair in published series vary from 4% to 29%. Different techniques for mesh
placement and variety of mesh and fixation material explains this wide range of recurrence
rate nevertheless, large series with standardized techniques report less than 4% of
recurrence rates.
Laparoscopic repair for incisional hernia is first published in 1993. Following reported
large personal series in recent years and evolution of adapted materiel, this technique
gained popularity.
The main difference between open and laparoscopic techniques is the reconstruction of the
abdominal wall. In all open techniques, abdominal wall is reconstructed (hernia edges
brought together) with reinforcement of the abdominal wall by a mesh inserted onlay, sublay
or inlay. In laparoscopic repair, the fascial defect is left in-situ but reinforced with a
mesh, overlapping largely the edges of hernia.
Advocated advantages of laparoscopy are: less abdominal wall dissection (less surgical
complications), tension-free mesh repair (no suturing), less postoperative pain, less
respiratory complications, shorter hospital stay, faster return to professional activity.
Disadvantages attributed to laparoscopic repair are the steep learning curve, high material
cost, longer operation times and rare but serious complications.
Large series and meta analyses confirmed the value of laparoscopic repair as at least equal
if not better compared with open repair. Most of the trials are focused on recurrence,
complication rate, hospital stay and sick leave. Only recently, quality of life and pain
started to be evaluated. No valuable data exists on chronic pain or persistent neuralgia,
body image, cosmesis or neuroticism neither after open nor the laparoscopic repair.
Chronic pain or persistent neuralgia has been recognized as a complication after inguinal
hernia repair but was reported in the 1980s as a rare and infrequent condition. Studies from
the mid 1990s have reported a higher frequency, with up to 50% of patients reporting pain
after hernia repair more than 1 year after surgery. Chronic pain after hernia repair can be
disabling, with considerable impact on quality of life. The natural history of postoperative
pain, including its prevalence, etiology, duration, associated disability and it's social
and economical impact remain undefined.
We know from our experience in inguinal hernia that chronic pain needs to be investigated
scrupulously to be identified. 20 to 27% chronic pain is associated to open repair in series
without specific questionnaires. Overall frequency of chronic pain is higher in studies with
specific measurements, where pain is the primary outcome of interest. Preoperative
psychological state of patient (depression, dependencies, drug consumption etc.) or history
of chronic pain with previous surgery or accident may be a predicting factor.
The definition of "chronic pain" by the International Association of the Study of Pain is
"pain lasting for 3 months or more". There is no a consensus on neither in the definition,
nor the severity grades of CSPOP in the literature. In our study chronic pain is defined as
a minimal score > 4 using the quadruple visual analogue scale (VASQ) 3 months after
procedure.
Somatic, and neuropathic chronic pain syndromes are described. Neuropathic pain usually
develops in the sensory distribution of an injured nerve. Chronic residual neuralgia occurs
as a result of surgical handing of sensory nerves. The nerve trauma can be due to partial or
complete division, stretching, contusion, crushing, electrical damage, or sutures
compression. Secondary nerve damage can occur due to irritation or compression by an
adjacent inflammatory process such as granuloma. Neuropathic pain described as pulling,
tugging, tearing, throbbing, stabbing, shooting, numbing, and dull. The onset of neuropathic
pain is often delayed, occurring after a latent period of days to weeks. Pain is often
aggravated by ambulation and sexual intercourse. Once chronic pain is installed, it does not
change without a radical treatment. Preoperative psychological state of patient (Depression,
dependencies, drug consumption etc.) or history of chronic pain with previous surgery or
accident may be a predicting factor.
The definition of ''Body image'' is given as person's perception of, satisfaction with, and
attitudes toward his or her body in general and to particular areas of the body. Little is
known about the subjective feelings and cosmetic consequences of scarring in patients who
undergo either conventional or laparoscopic abdominal surgery. Few data has been reported
about body image in patients with cancer, particular after mutilating operations such as
mastectomy. Three papers on ileocolectomy, proctectomy and live donor nephrectomy are
published by Dutch groups, comparing laparoscopy and laparotomy. Body image in presence of
an incisional hernia is certainly degraded before the surgery, unfortunately no baseline
data exists to date. Therefore, an hypothetic, relative, significant improvement in body
image by laparoscopic treatment compared to open repair needs to be evaluated.
The standard open technique in our institution has two declinations, the first technique is
retromuscular sublay and the second, open onlay mesh repair. In both techniques the fascial
defect is closed by suture repair with mesh reinforcement. Superiority of one of these
techniques compared to another is not proved, properly done, both achieve low recurrence
rates. Laparoscopic technique needs to meet widely accepted good-practice principles:
complete adhesiolysis between abdominal wall and viscera, use of specific bilayer mesh (non
adherent on the visceral surface), coverage of totality of the previous scar length with at
least 5cm overlap, adequate fixation.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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