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Original Article
12 (
3
); 156-159
doi:
10.1016/j.jor.2015.01.007

Outpatient minimally invasive spine surgery using endoscopy for the treatment of lumbar spinal stenosis among obese patients

Medical Research Department, Laser Spine Institute, LLC, Florida 33607, United States

∗Corresponding author: Elizabeth M. Hudak. ehudak@laserspineinstitute.com

Disclaimer:
This article was originally published by Reed Elsevier India Pvt. Ltd. and was migrated to Scientific Scholar after the change of Publisher.

Abstract

Abstract

The safety and effectiveness of outpatient endoscopic minimally invasive spinal surgery (MISS) for the treatment of lumbar spinal stenosis among obese patients is not well documented.

Pain, disability, and surgical variables were examined on 41 adult obese patients that underwent lumbar laminotomy and foraminotomy surgeries.

A significant decrease in pain and disability scores between preoperative and postoperative were found (p-value's < 0.001).

MISS using endoscopy can achieve sufficient decompression that results in a significant reduction in the level of pain and disability among obese patients with minimal blood loss and no complications.

Keywords

Body mass index (BMI)
Pain
Disability
Body weight
Decompression
1

1 Methods

1.1

1.1 Inclusion criteria

Analyses included patients who underwent lumbar laminotomy and foraminotomy surgery for the treatment of LSS during an 8-month period, who have not had previous lumbar surgery, did not have more than one moderate or severe level of LSS, over the age of 18, had complete preoperative and postoperative data, had a BMI ≥ 30.0, and were not classified as a worker's compensation case.

After implementing the inclusion criteria, 41 patients were eligible for participation in the study. The eligible sample consisted of adults between the ages of 20 and 72 years (M = 55.10, SD = 12.31). The sample was mostly male (68.3%) and Caucasian (92.7%). See Table 1 for demographic statistics.

Table 1 Demographics.
Demographics N = 41
Age in years (M (SD)) 55.10 (12.31)
Diabetes (% Non-diabetic) 82.9%
Smoker (% Non-smoker) 85.4%
Gender (% males) 68.3%
Race (% white) 92.7%
1.2

1.2 Outcome measures

In past spine surgery studies, the Visual Analog Scale (VAS) and Oswestry Disability Index (ODI) have been frequently used.9,10 In this study, the VAS was used to measure pain intensity. Patients were asked to rate their current level of pain ranging from 0 to 10 with 0 indicating no pain and 10 indicating the worst pain they can imagine. The ODI was used to measure patients' level of disability. For this measure, scores range from 0 to 100. Lower scores on the VAS and ODI indicate a lesser amount of pain and disability respectively.

1.3

1.3 Operative variables

Data pertaining to estimated blood loss (EBL), number of intraoperative and postoperative complications up to 30-days out (NOC), and length of surgery (LOS) were retrieved from patients' medical records.

1.4

1.4 Procedure

Patients who underwent a single-level laminotomy and foraminotomy for the treatment of LSS completed a VAS and ODI both preoperatively and 12-months postoperatively. Informed consent was obtained from all patients included in this study.

1.5

1.5 Surgical procedure

In brief, a scalpel was used to make a stab wound through which a guide-wire was inserted down to the facet region of the vertebral body. Over this guide-wire, the tissues were dilated with the use of a series of increasing diameter dilating tubes to approximately 18 mm. A drill bit was used to create a window into the lamina. This was confirmed through the use of fluoroscopy to determine the depth of penetration of the drill unit. Electrocautery and holmium lasers were used for hemocoagulation and soft tissue removal. Once this was accomplished, a standard mechanical burr system was utilized to grind away the lamina of the vertebral body and widen the opening that was created with the bit. Kerrison and pituitaries rongeurs were utilized during the entire process to assist in bone removal and for general debulking of soft tissues and loose bone fragments. Once the region of the lamina and foraminal canal was properly opened and decompressed, the tube was removed and the procedure was completed. All surgeries were performed in an outpatient setting.

2

2 Results

2.1

2.1 Missing data

Patients with missing data on the outcome measures were excluded from analyses. There was one missing data point for the EBL and NOC variables. There were no missing data points for the VAS, ODI, or LOS.

2.2

2.2 Outcome measures

An alpha level of 0.05 or below was considered statistically significant for all analyses. A significant decrease in VAS (p-value < 0.001) and ODI scores (p-value < 0.001) between preoperative and postoperative was observed. Descriptive statistics for the outcome measures are reported in Table 2. The average EBL was 59.00 mL and the LOS averaged at 78.46 min. There were no reported intraoperative or postoperative complications. See Table 3 for descriptive statistics and Figs. 1 and 2 for the frequency distribution of the surgical variables.

Table 2 Mean and standard deviations for outcome measures.
Variable M (SD)
VASa,b
Preoperative 6.70 (2.41)
Postoperative 2.54 (2.62)
ODIa,b
Preoperative 45.51 (11.17)
Postoperative 20.54 (17.75)
Significantly lower scores between Preoperative and Postoperative; p-value < 0.001.
Lower scores reflect better performance.
Table 3 Estimated blood loss and length of surgery descriptives.
Variable N Minimum Maximum Mean Standard deviation
EBL (mL) 40 10.00 300.00 59.00 57.68
LOS (minutes) 41 22 167 78.46 36.61
Estimated blood loss.
Fig. 1 Estimated blood loss.
Length of surgery.
Fig. 2 Length of surgery.
3

3 Discussion

This study demonstrates that MISS using endoscopy can achieve sufficient decompression that results in a significant reduction in level of pain and disability among obese patients with minimal blood loss and no complications.

The findings reported in this study are comparable with other studies that examine weight and lumbar MISS. For example, a study by Rosen and colleagues13 found that among obese patients that underwent a minimally invasive lumbar fusion, body habitus (as measured by BMI) did not have a significant relationship with outcomes measures that included the VAS, ODI, and number of complications. Thus, our results support previous studies indicating that obesity is not a contraindication to MISS.

Although our study examined outcomes one year postoperative, our findings are consistent with another study that examined outcomes four years postoperative. Using the sample from the Spine Patient Outcome Research Trial (SPORT), Rihn and colleagues14 found that at four years postoperative, obesity did not affect the primary outcomes which included the bodily pain and physical function domains of the 36-Item Short Form Health Survey (SF-36) and the American Academy of Orthopaedic Surgeons MODEMS (Musculoskeletal Outcomes Data Evaluation and Management System) version of the ODI of those treated operatively for LSS.

Other MISS studies produced similar results to ours.12,15 For example, Senker and colleagues15 examined patients who underwent a lumbar MISS fusion or laminotomy. Results found no difference in the complication rate, blood loss, drainage, or length of hospital stay between the normal weight (BMI < 25), overweight (BMI > 25 and < 30), and obese (BMI > 30) patients. Our study supports the notion that the minimally invasive approach helps to minimize the number of complications among obese patients.

As with any study, this one is not without limitations. First, although the BMI calculation measure is well correlated with the degree of adiposity and simple to measure, BMI does not measure total body fat percentage because it cannot distinguish between fat-free mass (bones and muscles) and fat mass. Studies suggest that body habitus plays a role in complications and that BMI does not necessarily correlate with the depth of subcutaneous tissue. Thus, the measurement of weight is an all-inclusive measure rather than just a measure of fat. Second, although the surgeons can visually confirm decompression during surgery, this study does not include radiographic results for confirmation. Thus, conclusions can only be drawn from data pertaining to the self-reported outcomes. Third, our findings are limited due to the lack of a control group. This prevents an adequate comparison between obese patients that undergo an endoscopic MISS procedure versus an open fusion. Even without this direct comparison, the results of this study provide support for the safety of endoscopic MISS procedures.

This study demonstrates that the minimally invasive procedure performed in this study provides sufficient decompression that reduces levels of pain and disability among obese patients with no complications and minimal blood loss. Obese patients should consider minimally invasive endoscopic procedures for the treatment of LSS to achieve adequate decompression resulting in significant improvements in pain and disability with a low rate of complications.

Conflicts of interest

All authors have none to declare.

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