The clinical course of acute, subacute and persistent low back pain: a systematic review and meta-analysis

被引:0
作者
Wallwork, Sarah B. [1 ]
Braithwaite, Felicity A. [1 ,2 ]
OKeeffe, Mary [3 ]
Travers, Mervyn J. [4 ]
Summers, Simon J. [5 ]
Lange, Belinda [6 ]
Hince, Dana A. [7 ]
Costa, Leonardo O. P. [8 ]
da C. Menezes Costa, Luciola
Chiera, Belinda [9 ]
Moseley, G. Lorimer [1 ]
机构
[1] Univ South Australia, IIMPACT Hlth, Adelaide, SA, Australia
[2] South Australian Hlth & Med Res Inst SAHMRI, Hopwood Ctr Neurobiol, Persistent Pain Res Grp, Adelaide, SA, Australia
[3] Univ Sydney, Inst Musculoskeletal Hlth, Fac Med & Hlth, Sch Publ Hlth, Sydney, NSW, Australia
[4] Univ Notre Dame Australia, Sch Hlth Sci & Physiotherapy, Fremantle, Australia
[5] Queensland Univ Technol, Sch Biomed Sci, Brisbane, Qld, Australia
[6] Flinders Univ S Australia, Caring Futures Inst, Coll Nursing & Hlth Sci, Adelaide, SA, Australia
[7] Univ Notre Dame, Inst Hlth Res, Fac Med Nursing Midwifery & Hlth Sci, Fremantle, Australia
[8] Univ Cidade Sao Paulo, Masters & Doctoral Programs Phys Therapy, Sao Paulo, Brazil
[9] Univ South Australia, UniSA STEM, Adelaide, SA, Australia
基金
英国医学研究理事会;
关键词
QUALITY-OF-LIFE; PRIMARY-CARE; PROGNOSTIC-FACTORS; INCEPTION COHORT; ACUTE EPISODE; LONGITUDINAL ANALYSIS; PSYCHOSOCIAL FACTORS; GENERAL-PRACTICE; RISK-FACTORS; FOLLOW-UP;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Understanding the clinical course of low back pain is essential to informing treatment recommendations and patient stratification. Our aim was to update our previous systematic review and meta-analysis to gain a better understanding of the clinical course of acute, subacute and persistent low back pain. Methods: To update our 2012 systematic review and meta-analysis, we searched the Embase, MEDLINE and CINAHL databases from 2011 until January 2023, using our previous search strategy. We included prospective inception cohort studies if they reported on participants with acute (< 6 wk), subacute (6 to less than 12 wk) or persistent (12 to less than 52 wk) nonspecific low back pain at study entry. Primary outcome measures included pain and disability (0-100 scale). We assessed risk of bias of included studies using a modified tool and assessed the level of confidence in pooled estimates using the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) tool. We used a mixed model design to calculate pooled estimates (mean, 95% confidence interval [CI]) of pain and disability at 0, 6, 12, 26 and 52 weeks. We treated time in 2 ways: time since study entry (inception time uncorrected) and time since pain onset (inception time corrected). We transformed the latter by adding the mean inception time to the time of study entry. Results: We included 95 studies, with 60 separate cohorts in the systematic review (n = 17 974) and 47 cohorts (n = 9224) in the meta-analysis. Risk of bias of included studies was variable, with poor study attrition and follow-up, and most studies did not select participants as consecutive cases. For the acute pain cohort, the estimated mean pain score with inception time uncorrected was 56 (95% CI 49-62) at baseline, 26 (95% CI 21-31) at 6 weeks, 22 (95% CI 18-26) at 26 weeks and 21 (95% CI 17-25) at 52 weeks (moderate-certainty evidence). For the subacute pain cohort, the mean pain score was 63 (95% CI 55-71) at baseline, 29 (95% CI 22-37) at 6 weeks, 29 (95% CI 22-36) at 26 weeks and 31 (95% 23-39) at 52 weeks (moderate-certainty evidence). For the persistent pain cohort, the mean pain score was 56 (95% CI 37-74) at baseline, 48 (95% CI 32-64) at 6 weeks, 43 (95% CI 29-57) at 26 weeks and 40 (95% CI 27-54) at 52 weeks (very low-certainty evidence). The clinical course of disability was slightly more favourable than the clinical course of pain. Interpretation: Participants with acute and subacute low back pain had substantial improvements in levels of pain and disability within the first 6 weeks ( moderate-certainty evidence); however, participants with persistent low back pain had high levels of pain and disability with minimal improvements over time (very low-certainty evidence). Identifying and escalating care in individuals with subacute low back pain who are recovering slowly could be a focus of intervention to reduce the likelihood of transition into persistent low back pain. Protocol registration: PROSPERO - CRD42020207442
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页码:E29 / E46
页数:18
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