Predictors of instanteous relief from spinal manipulation for non-specific low back pain: a delphi study

Stanley Innes, Amber Beynon, Christopher Hodgetts, Rachel Manassah, Denyse Lim & Bruce F. Walker
Chiropractic & Manual Therapies volume 28, Article number: 39 (2020)

Abstract
Background
There is some evidence and anecdotal reports that high-velocity low-amplitude (HVLA) spinal manipulation therapy (SMT) for non-specific low back pain (NSLBP) may immediately reduce pain in some patients. The mechanism for such a change remains unclear and the evidence is conflicting. The aim of this study was to seek consensus among a sample of expert manual therapists as to the possible clinical predictors that could help identify patients who are most likely to receive instant relief from NSLBP with SMT intervention.

Methods
Thirty-seven expert chiropractors and manipulative physiotherapists from around the world were invited to participate in a three round online Delphi questionnaire during the second half of 2018. Participants were provided with a list of 55 potential signs and symptoms as well as offering them the option of suggesting other factors in the first round. The variables were rated using a 4-point Likert likelihood scale and a threshold of 75% agreement was required for any item to progress to the next round.

Results
Of these 37 experts, 19 agreed to participate. Agreement as to the proportion of patients who receive instantaneous relief was minimal (range 10–80%). A total of 62 items were ranked over the 3 rounds, with 18 of these retained following the third round. The highest rated of the 18 was ‘A history including a good response to previous spinal manipulation’.

Discussion/conclusion
Five categories; patient factors, practitioner factors, signs and symptoms of NSLBP presentation, an instrument of measurement (FABQ), and the presence of cavitation following SMT best describe the overall characteristics of the factors. The 18 factors identified in this study can potentially be used to create an instrument of measurement for further study to predict those patients with NSLBP who will receive instantaneous relief post-SMT.

Journal Reference

From the DISCUSSION section of the study:

It appears logical that the most highly rated predictive factor for a patient to experience an instantaneous positive response to HVLA SMT for NSLBP was “a history that included a good response to previous spinal manipulation”.

The items, “A patient with high trust and confidence in the practitioner”, “a good patient-practitioner relationship”, “patient has comprehensive understanding of a condition” and “practitioner understanding of patient expectations” were all highly agreed upon predictors and reflect known aspects of a therapeutic alliance.

There were two items in the final list that were in accord with factors known to impact negatively on outcomes of patients experiencing LBP. These were the presence of co-morbidities [37, 38] (“opinion of health status”) and psychosocial factors [39] (“FABQ Work scale”).

The items of “patient susceptible to placebo effect” and “the production of a clicking sound (cavitation) at the moment of thrust”, although not linked by the experts in this study, could possibly be viewed together. The thrust component without a cavitation can reduce spinal pain [41]. However, there is also evidence that, at least in part, the audible sound produces a placebo effect.

While many items were thought to be impacted on by psychosocial factors there was nonetheless a considerable number with a biomechanical focus. Three of the five criteria for the clinical prediction rule for identifying patients with non-radicular low back pain who will benefit from SMT [48] were retained and indicated a milder less complicated profile i.e., pain shorter in duration, no radiculopathy or fear-avoidance issues, and reduced or painful (end) ranges of motion. While there is some evidence that patient self-reported changes in motion were predictive of post-SMT immediate improvement [49], the reliability and validity of altered ranges of movement or pain provocation is yet to be demonstrated in clinical trials and is thought to require advanced studies to inform their clinical utility.

 

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