Relationship between systemic inflammation and recovery over 12 months after an acute episode of low back pain.

Author(s):  
David M. Klyne ◽  
Mary F. Barbe ◽  
Paul W. Hodges
PLoS ONE ◽  
2007 ◽  
Vol 2 (8) ◽  
pp. e706 ◽  
Author(s):  
Emmanuel Coudeyre ◽  
Florence Tubach ◽  
François Rannou ◽  
Gabriel Baron ◽  
Fernand Coriat ◽  
...  

2017 ◽  
Vol 71 ◽  
pp. 75-82 ◽  
Author(s):  
Juliano Bergamaschine Mata Diz ◽  
Bruno de Souza Moreira ◽  
Diogo Carvalho Felício ◽  
Luiza Faria Teixeira ◽  
Fabianna Resende de Jesus-Moraleida ◽  
...  

2021 ◽  
Author(s):  
Okan Günaydın ◽  
Elzem Bolkan Günaydın

Aim: To compare the hematological parameters associated with systemic inflammation between acute and subacute/chronic nonspecific low back pain and to evaluate their diagnostic roles in relation to chronicity in low back pain. Materials & methods: This retrospective case–control study included 150 participants aged 18–65 years with acute nonspecific low back pain, 150 with subacute/chronic nonspecific low back pain, 150 as the control group. Results: Red cell distribution width was significantly higher in the subacute/chronic pain group compared with the acute pain group (p = 0.003), and had a poor diagnostic value for chronicity (Cutoff: 11.95, p = 0.003). There were no significant differences in terms of other parameters (p > 0.05). Conclusion: Red cell distribution width has a poor diagnostic value for chronicity in nonspecific low back pain.


2017 ◽  
Vol 97 (9) ◽  
pp. 889-895 ◽  
Author(s):  
Gustavo C. Machado ◽  
Chris G. Maher ◽  
Paulo H. Ferreira ◽  
Jane Latimer ◽  
Bart W. Koes ◽  
...  

Pain ◽  
2010 ◽  
Vol 151 (1) ◽  
pp. 1-2
Author(s):  
Andrea D. Furlan ◽  
Nancy Carnide

2021 ◽  
Author(s):  
Luke Christopher Jenkins ◽  
Wei-Ju Chang ◽  
Valentina Buscemi ◽  
Matthew Liston ◽  
Peter Humburg ◽  
...  

Predicting the development of chronic low back pain (LBP) at the time of an acute episode remains challenging. The Understanding persistent Pain Where it ResiDes (UPWaRD) study aimed to identify neurobiological and psychological risk factors for chronic LBP. Individuals with acute LBP (N=120) participated in a prospective cohort study with six-month follow-up. Candidate predictors were selected from the neurobiological (e.g. sensorimotor cortical excitability assessed by sensory and motor evoked potentials, Brain Derived Neurotrophic Factor genotype), psychological (e.g. depression and anxiety), symptom-related (e.g. LBP history) and demographic domains. Analyses involved multivariable linear regression models with pain intensity or disability degree as continuous variables. Secondary analyses involved a multivariable logistic model with presence of low back pain at six months (thresholding pain intensity and disability degree) as a dichotomous variable. Lower sensory cortex and corticomotor excitability, higher baseline pain intensity, higher depression, stress and pain catastrophizing were the strongest predictors (R2=0.47) of pain intensity at six months. Older age and higher pain catastrophizing were the strongest predictors (R2=0.30) of disability at six months. When LBP outcome was dichotomised, sensory cortex and corticomotor excitability, BDNF genotype, depression and anxiety, LBP history and baseline pain intensity, accurately discriminated those who did and did not report LBP at six months (c-statistic 0.91). This study identifies novel risk factors for future LBP after an acute episode that can predict an individuals pain intensity and level of disability at six-month follow-up, and accurately discriminate between those who will and will not report LBP at six months.


2017 ◽  
Vol 96 (8) ◽  
pp. 535-540 ◽  
Author(s):  
Bárbara Zille Queiroz ◽  
Daniele Sirineu Pereira ◽  
Nayza Maciel de Britto Rosa ◽  
Renata Antunes Lopes ◽  
André Gustavo Pereira Andrade ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document