This study aims to compare the results of two mini invasive surgical approaches in abdominal aortic surgery: mini lumbotomy with retroperitoneal approach versus mini laparotomy with transperitoneal approach. Respiratory and renal functions and recovery of intestinal transit will be assessed after 30 days. The secondary purpose of this study is to assess the life quality and morbi-mortality at 30 days, as well as at 6 and 12 months.
Following abdominal aortic surgery, post-operative outcomes are considered favorable with a rapid recovery of respiratory, renal functions and intestinal transit, with limited cardiac events. Complications are still frequent after the classic open abdominal surgery. In abdominal aortic surgery, "mini" abdominal incision has been proposed as an alternative to the classic large surgical approach. Two mini surgical approaches are possible: mini lumbotomy with retroperitoneal approach, and mini laparatomy with transperitoneal approach. Previous studies have only compared classic versus mini surgical approaches and many are retrospectives studies. Pain control through the mini-incision surgery allowed early mobilization of patients, improved lung function, reduced muscle loss, and favoured intestinal motility. So far, no study has compared the results of two mini invasive aortic approaches. The aim of this prospective randomized study is to compare two mini-invasive surgical approaches and to determine which of them allows the improvement of surgical outcomes with less morbi-mortality.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
206
The patient will be positioned supine. After induction of general anesthesia, a median umbilical incision will be performed. The average length of the incision of the laparotomy will be 10 cm (8-12 cm). The small intestine will be then mobilized medially and held by an orthostatic retractor. Arterial dissection and control as well as bypasses will be performed according to the conventional technique. In case of occlusive disease of the iliac arteries, femoral site will be selected to achieve the distal anastomoses of the bifurcated prosthetic graft.
After induction of general anesthesia, the patient will be positioned in right lateral decubitus at 45° of the table plane. The incision will be performed from the tip of the eleventh rib with a slightly sloping path to the outer edge of the rectus muscle. The average length of the incision of the laparotomy will be 10 cm (8-12 cm). Abdominal aorta will be approached retroperitoneally. Arterial dissection and control as well as bypasses will be performed according to the conventional retroperitoneal technique. In case of occlusive disease of the iliac arteries, femoral site will be selected to achieve the distal anastomoses of the bifurcated prosthetic graft.
Respiratory recovery
evaluated with respiratory function test (Sniff nasal inspiratory pressure, SNIP test)
Time frame: day 30
Renal recovery
evaluated by blood creatinine level, uremia and kalemia
Time frame: day 30
Intestinal transit recovery
evaluated by reapparition of gas and transit
Time frame: day 30
Respiratory recovery
evaluated by SNIP test
Time frame: day 1
Respiratory recovery
evaluated by SNIP test
Time frame: day 3
Respiratory recovery
evaluated by SNIP test
Time frame: day 5
Renal recovery
evaluated by creatinine clearance, uremia and kaliemia
Time frame: day 1
Renal recovery
evaluated by creatinine clearance, uremia and kaliemia
Time frame: day 3
Renal recovery
evaluated by creatinine clearance, uremia and kaliemia
Time frame: day 5
Intestinal recovery
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assessment of intestinal transit (stool emission)
Time frame: day 1
Intestinal recovery
assessment of intestinal transit (stool emission)
Time frame: day 3
Intestinal recovery
assessment of intestinal transit (stool emission)
Time frame: day 5
Post-operative pain assessment
with VAS scale
Time frame: day 1
Post-operative pain assessment
with VAS scale
Time frame: day 3
Post-operative pain assessment
with VAS scale
Time frame: day 5
Quality of life assessment
by using SF-12 questionnaire
Time frame: after 6 months
Quality of life assessment
by using SF-12 questionnaire
Time frame: after 1 year
Morbi-mortality
evaluated by EQ-5D questionnaire
Time frame: after 6 months
Morbi-mortality
evaluated by EQ-5D questionnaire
Time frame: after 1 year
Morbi-mortality
evaluated by non-recovery of functions, eventration and death
Time frame: day 30