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Observational Study
. 2016 Apr 5;315(13):1362-71.
doi: 10.1001/jama.2016.3010.

Change in Pain and Physical Function Following Bariatric Surgery for Severe Obesity

Affiliations
Observational Study

Change in Pain and Physical Function Following Bariatric Surgery for Severe Obesity

Wendy C King et al. JAMA. .

Abstract

Importance: The variability and durability of improvements in pain and physical function following Roux-en-Y gastric bypass (RYGB) or laparoscopic adjustable gastric banding (LAGB) are not well described.

Objectives: To report changes in pain and physical function in the first 3 years following bariatric surgery, and to identify factors associated with improvement.

Design, setting, and participants: The Longitudinal Assessment of Bariatric Surgery-2 is an observational cohort study at 10 US hospitals. Adults with severe obesity undergoing bariatric surgery were recruited between February 2005 and February 2009. Research assessments were conducted prior to surgery and annually thereafter. Three-year follow-up through October 2012 is reported.

Exposures: Bariatric surgery as clinical care.

Main outcomes and measures: Primary outcomes were clinically meaningful presurgery to postsurgery improvements in pain and function using scores from the Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36) (ie, improvement of ≥5 points on the norm-based score [range, 0-100]) and 400-meter walk time (ie, improvement of ≥24 seconds) using established thresholds. The secondary outcome was clinically meaningful improvement using the Western Ontario McMaster Osteoarthritis Index (ie, improvement of ≥9.7 pain points and ≥9.3 function points on the transformed score [range, 0-100]).

Results: Of 2458 participants, 2221 completed baseline and follow-up assessments (1743 [78.5%] were women; median age was 47 years; median body mass index [BMI] was 45.9; 70.4% underwent RYGB; 25.0% underwent LAGB). At year 1, clinically meaningful improvements were shown in 57.6% (95% CI, 55.3%-59.9%) of participants for bodily pain, 76.5% (95% CI, 74.6%-78.5%) for physical function, and 59.5% (95% CI, 56.4%-62.7%) for walk time. Additionally, among participants with severe knee or disability (633), or hip pain or disability (500) at baseline, approximately three-fourths experienced joint-specific improvements in knee pain (77.1% [95% CI, 73.5%-80.7%]) and in hip function (79.2% [95% CI, 75.3%-83.1%]). Between year 1 and year 3, rates of improvement significantly decreased to 48.6% (95% CI, 46.0%-51.1%) for bodily pain and to 70.2% (95% CI, 67.8%-72.5%) for physical function, but improvement rates for walk time, knee and hip pain, and knee and hip function did not (P for all ≥.05). Younger age, male sex, higher income, lower BMI, and fewer depressive symptoms presurgery; no diabetes and no venous edema with ulcerations postsurgery (either no history or remission); and presurgery-to-postsurgery reductions in weight and depressive symptoms were associated with presurgery-to-postsurgery improvements in multiple outcomes at years 1, 2, and 3.

Conclusions and relevance: Among a cohort of participants with severe obesity undergoing bariatric surgery, a large percentage experienced improvement, compared with baseline, in pain, physical function, and walk time over 3 years, but the percentage with improvement in pain and physical function decreased between year 1 and year 3.

Trial registration: clinicaltrials.gov Identifier: NCT00465829.

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Conflict of interest statement

Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr Coucourlas reports receipt of research grants from Covidien, Ethicon, Nutrisystem, and PCORI; and consultant fees from Apollo Endosurgery. Dr Dakin reports receipt of consultant fees from Covidien. Dr Pories reports receipt of research grants from Johnson & Johnson Janssen Pharmaceuticals. Dr Wolfe reports receipt of consultant fees from EnteroMedics. Dr Flum reports having had an advisor role with Pacira Pharmaceuticals, providing expert testimony for Surgical Consulting LLC, and receiving travel expenses from PCORI. The other authors report no disclosures.

Figures

Figure 1
Figure 1. Longitudinal Assessment of Bariatric Surgery-2 (LABS-2) Study Flow From Approached Patients to Analysis Sample
a The number of patients initially screened for eligibility was not recorded. b Indicates that all pain and function measures may not have been completed.
Figure 2
Figure 2. Back and Leg Pain Before and After Bariatric Surgery
Observed data are reported in eTable 2. a Patients were asked, “In the past 4 weeks, how much did pain interfere with your normal work, including both work outside the home and house work?” Those who reported having no back or leg pain to the preceding question were grouped with those reporting “not at all.” b Sample size of model. Modeled data, adjusted for age and site are shown. c Patients were asked, “If you had to spend the rest of your life with the symptoms you have right now, how would you feel about it?” Those who reported no back or leg pain to the preceding question were grouped with those reporting “very satisfied.”

Comment in

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