Protocol: Prospective cohort study investigating the impact of muscle degeneration on low back pain after lumbar decompression

Author:

Gotfryd Alberto Ofenhejm1,Antonioli Eliane1,Couri Pedro Henrique Cortat Proba1,Castro Adham Amaral e2,Machado Luciana Pereira Magalhaes2,Gomes Amanda Maradini Narciso1,Miranda Frederico Celestino2,Baptista Eduardo2,Barros Durval Carmo Santos2,Rosemberg Laercio Alberto2,Lenza Mario1

Affiliation:

1. Programa Locomotor, Hospital Israelita Albert Einstein

2. Hospital Israelita Albert Einstein

Abstract

Abstract

Background The main reason for surgical procedures in the lumbar spine is nerve compression associated with radiculopathy or neurogenic claudication. Lumbar surgical decompression is effective in relieving neurogenic pain and restoring walking ability. However, the presence of associated preoperative low back pain (LBP) in patients with neurological symptoms is not uncommon, and its management is still controversial. Chronic dysfunctions, such as atrophy and muscle fat replacement of the main spine muscles, are related to pain intensity. These dysfunctions can be identified and measured by means of magnetic resonance imaging (MRI) as muscle fat infiltration and reduction of muscular cross-sectional area. The primary objective of this study was to correlate the degree of muscle degeneration with the presence of LBP before lumbar decompression surgery. The secondary objectives are evaluations of the impact of different surgical techniques in muscle degeneration, as well as of the association of pain, disability, quality life and psychosocial factors during recovery after lumbar decompression surgery. Methods This prospective cohort will include individuals older than 18 years who underwent surgical lumbar decompression. Radiographic exams and MRI examinations will be performed before the surgical procedure. Changes in scores of pain, kinesiophobia, psychosocial risk prognosis, perception of improvement, anxiety, depression, disability and quality of life will be measured at baseline and at 3, 6, 12 and 24 months of follow-up. The primary outcome will be the intensity of LBP. Study status Protocol Trial version: 02 Date: Feb 10, 2021 Recruitment Start Date: January 2020 Recruitment Estimated End Date: December/2025 Status: Recruiting Trial registration number: NCT04273828

Publisher

Research Square Platform LLC

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