Hernia Clinical Trial
Official title:
Posincisional Hernia Prevention. Effectiveness of Reinforced Tension Line (RTL) Technique Compared With the Conventional Method
The posincisional hernia is considered a delicate complication , with an incidence of 10-12%
in patients undergoing laparotomy may reach 45% in case of emergency and high-risk patients
. It is estimated that in the United States are made about a million of reoperations for
correction of this complication , with millions and despite the myriad studies that have
been done in recent years there has been a decrease in the incidence losses and mortality of
this complication.
Given the seriousness of this problem the last global consensus guidelines sent to the
surgical community in three main areas: Identify the importance of the problem, improve the
theoretical knowledge and technical capacity in the closure of the abdominal wall and
Implement prophylaxis in selected patients.
The technique of reinforced tension line (RTL) was proposed by hollinsky and collaborators
and is a strengthening of the abdominal incision with placement of a suture that runs
lateral to the edge of the incision and closure of the abdominal wall is performed the usual
manner with the only surgete continuous suture for closure is placed lateral to the suture
reinforcement.
In the present study may contribute to these guidelines and to groups of patients at high
risk were identified and applying the RTL technique and demonstrate that its use is safe and
useful in reducing the presence of this complication could be implemented as prophylaxis
handling the same .
The RTL method was applied experimentally on bodies to close the abdominal wall also be used
in a cohort of patients for hernia repair wall , showing that by using it the abdominal wall
is more resistant to shear forces by theoretical foundation that exists to show that could
prevent the development of incisional hernias. There are no studies in the literature
comparing this technique against conventional methods of closure of the abdominal wall as to
the prevention of the same.
The patient at the time of scheduled surgery either electively or urgently where planned
preoperatively making approach by midline is invited to participate in the study, family and
patient reported the details thereof and shall be obtained informed consent to participate.
The patient will be included in the experimental group (RTL) or (conventional) control
according to a list of random numbers.
Estimated Enrollment: 76 Study Start Date July 2014 Estimated study completion date: May
2015 Estimated Primary Completion Date: January 2015.
Arms. Assigned interventions. Experimental: Procedure/ Surgery. Method RTL. The method
consists of two lines of suture, each, over the fascial wound edge. It starts with a suture
strand (in this study was used PDS number 0) in one end of the fascial wound where the
suture is run longitudinally and parallel to the aponeurotic edge. The needle should go in
and out at intervals of 1 cm away and always kept at 0.5 cm from the edge of the fascia.
Upon reaching the opposite angle of the wound suture strand another repeating the same
process on the fascial edge otherwise used. The ends of the two suture strands are tied in
fascial angles.
Thus the fascial wound is sutured with two lines of strengthening its edges. Then proceed to
close the wound with continuous súrgete always ensuring that the suture lines remain
anchored on suture reinforcement.
Other Conventional midline mass closure technique. Upon completion of the surgical procedure
was the closure of abdominal wall which will be made with the number 0 monofilament PDS,
starting with knot at one end of the wound, continuous with continuous súrgete, moving each
point to a centimeter away from the other. Each point will be a distance of one centimeter
from the edge of the fascia. At the opposite end of the wound the same procedure was
initiated and found the two suture lines at the midpoint of the wound will proceed to tying
the two sutures with 4 square knots.
Participants surgeons evaluate the patient in the postoperative monitoring prior to hospital
discharge , searching data hernia . After hospital discharge , participants surgeons
evaluate the patient in the first external consultation with the attending surgeon looking
data incisional hernia. Follow-up time will be 6 months which will be held in the outpatient
and 6 months a CT will be made to identify the presence of incisional hernia
variables
Main outcome : presence of incisional hernia ( dichotomous categorical )
Secondary outcome : presence of complications of surgical wound ; infection , hematoma ,
ecchymosis , seroma ( categorical nominal)
Main predictor : technique for closure of the abdominal wall ( dichotomous categorical )
Conformation : gender ( dichotomous ) , age ( categorical nominal) , comorbidities (
categorical nominal) , emergency surgery ( dichotomous ), cough ( dichotomous ) , type of
surgery ( categorical nominal) .
The presence of incisional hernia will be defined as loss of continuity of the abdominal
wall after surgical closure , with the formation of a peritoneal sac and the protrusion of
different structures of the cavity. Is clinically defined by the presence of a lump in the
region of the surgical wound secondary to a physical effort as well as palpation of a defect
in the continuity of the wound in the abdominal wall. The gold standard for diagnosis will
be computed tomography in which the area of the disruption will be evaluated as well as the
size and the organs involved , which will define the tomographic sign is the separation
distance of the upright which should not be greater than 25 mm .
The present Study be made performed at the Hospital Regional de Alta Especialidad del Bajio.
Population. Patients over 18 years of age undergoing diagnostic laparotomy regardless of
whether background urgent or scheduled at high risk for developing incisional hernia.
Universe:
Laparotomy patients scheduled for either elective or emergency with risk factors for
developing incisional hernia.
Calculation of sample:
The sample size was calculated based on the study of Van Ramshorts, which found 40% of
incisional hernia in patients at high risk with a score higher than 6 as the predictor
scale, against 12% for the submission of the same in high-risk patients, earning a total of
76 patients, divided into 2 groups of 38 patients for each of the techniques, considering
able to detect a difference of at least 28% in the proportion of patients without hernia,
with 80% power and an alpha of 0.5% with two tails.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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