scholarly journals The Effect of Body Mass Index on Intra-Abdominal Pressure and Blood Loss in Lumbar Spine Surgery

2012 ◽  
Vol 51 (2) ◽  
pp. 81 ◽  
Author(s):  
In Ho Han ◽  
Dong Wuk Son ◽  
Kyoung Hyup Nam ◽  
Byung Kwan Choi ◽  
Geun Sung Song
2018 ◽  
Vol 18 (7) ◽  
pp. 1204-1210 ◽  
Author(s):  
Olivia J. Bono ◽  
Gregory W. Poorman ◽  
Norah Foster ◽  
Cyrus M. Jalai ◽  
Samantha R. Horn ◽  
...  

2009 ◽  
Vol 10 (2) ◽  
pp. 145-153 ◽  
Author(s):  
Peyman Pakzaban

Object The design and utilization of a novel device for noninvasive preincision localization of the target spine segment during lumbar spine surgery is presented. Methods The device consists of 4 low-energy laser diodes, emitting planar beams, mounted around the perimeter of a ring at right angles to each other. The beams are used to align 2 radiopaque cables hanging off the sides of the patient with the target spine segment and the radiographic source and film. The performance of the device in guiding the placement of the skin incision was prospectively evaluated in 76 consecutive patients undergoing unilateral 1-level microsurgical lumbar laminotomy. Preincision lateral radiographs obtained with the device were compared with postincision localizing radiographs in all patients. Results In all patients, the location of the incision guided by the final preincision radiograph was found to precisely overlie the target segment as confirmed by a postincision radiograph, the latter obtained after exposure of the underlying laminae. In no instance was it necessary to extend the incision, modify the surgical trajectory, or repeat the postincision radiograph due to improper incision placement. The device's radiopaque cables were clearly visualized on radiography as they traversed the spine image, regardless of body mass index. The initial preincision radiograph based on the surgeon's estimate of the location of the target site localized the target segment in 58 patients (76.3%) and an adjacent segment in the remaining 18 patients (23.7%). Accuracy of the surgeon's initial estimate of the target site (but not accuracy of the device) was found to be inversely associated with body mass index (p < 0.001), thickness of the subcutaneous fat layer overlying the spine (p < 0.001), and presence of transitional lumbosacral anatomy (p = 0.03). Conclusions The localization device presented herein provides accurate noninvasive localization of the target spine segment and guides precise placement of the incision over the target segment during lumbar spine surgery.


Spine ◽  
2014 ◽  
Vol 39 (10) ◽  
pp. 798-804 ◽  
Author(s):  
Alejandro Marquez-Lara ◽  
Sreeharsha V. Nandyala ◽  
Sriram Sankaranarayanan ◽  
Mohamed Noureldin ◽  
Kern Singh

2019 ◽  
Vol 31 (2) ◽  
pp. 194-200 ◽  
Author(s):  
Signe Elmose ◽  
Mikkel Ø. Andersen ◽  
Else Bay Andresen ◽  
Leah Yacat Carreon

OBJECTIVEThe purpose of this study was to investigate the effect of tranexamic acid (TXA) compared to placebo in low-risk adult patients undergoing elective minor lumbar spine surgery—specifically with respect to operative time, estimated blood loss, and complications. Studies have shown that TXA reduces blood loss during major spine surgery. There have been no previous studies on the effect of TXA in minor lumbar spine surgery in which these variables have been evaluated.METHODSThe authors enrolled patients with ASA grades 1 to 2 scheduled to undergo lumbar decompressive surgery at Middelfart Hospital into a double-blind, randomized, placebo-controlled, parallel-group study. Patients with thromboembolic disease, coagulopathy, hypersensitivity to TXA, or a history of convulsion were excluded. Patients were randomly assigned, in blocks of 10, to one of 2 groups, TXA or placebo. Anticoagulation therapy was discontinued 2–7 days preoperatively. Prior to the incision, patients received either a bolus of TXA (10 mg/kg) or an equivalent volume of saline solution (placebo). Independent t-tests were used to compare differences between the 2 groups, with statistical significance set at p < 0.05.RESULTSOf the 250 patients enrolled, 17 patients were excluded, leaving 233 cases for analysis (117 in the TXA group and 116 in the placebo group). The demographics of the 2 groups were similar, except for a higher proportion of women in the TXA group (TXA 50% vs placebo 32%, p = 0.017). There was no significant between-groups difference in operative time (49.53 ± 18.26 vs 54.74 ± 24.49 minutes for TXA and placebo, respectively; p = 0.108) or intraoperative blood loss (55.87 ± 48.48 vs 69.14 ± 83.47 ml for TXA and placebo, respectively; p = 0.702). Postoperative blood loss measured from drain output was 62% significantly lower in the TXA group (13.03 ± 21.82 ml) than in the placebo group (34.61 ± 44.38 ml) (p < 0.001). There was no significant difference in number of dural lesions or postoperative spinal epidural hematomas, and there were no thromboembolic events.CONCLUSIONSTranexamic acid did not have a statistically significant effect on operative time, intraoperative blood loss, or complications. This study gives no evidence to support the routine use of TXA during minor lumbar decompressive surgery.Clinical trial registration no.: NCT03714360 (clinicaltrials.gov)


2019 ◽  
Vol 0 (3.98) ◽  
pp. 80-84
Author(s):  
M.V. Lyzohub ◽  
M.A. Georgiyants ◽  
K.I. Lyzohub

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