MD, PhD, MAE, FMedSci, FRCP, FRCPEd.
This up-date of a Cochrane Review evaluated the benefits and harms of SMT compared to (1) sham SMT/placebo intervention, (2) no treatment, and (3) other conservative interventions in people with chronic LBP (18+ years old).
The authors searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, Embase, two other databases, and two trial registers up to 18 October 2024, unrestricted by language. They also screened the reference lists of all included studies and relevant systematic reviews, and approached content experts to identify potentially missing studies. They included randomised controlled trials (RCTs) that examined the effect of spinal manipulation or mobilisation in adults with chronic LBP compared to sham SMT/placebo, no treatment, and other conservative interventions. They placed no restrictions on the setting. We excluded studies that exclusively examined sciatica. The critical outcomes were pain, functional status, and adverse events. The primary time point was one month for pain and functional status. We evaluated adverse events at the end of the intervention. Bias in the included studies was assessed using the original Cochrane risk of bias tool (RoB 1).
Seventy‐six RCTs (11,866 participants) met the inclusion criteria, 50 (66%) of which were not included in the previous version of this review. Seventeen trials (2021 participants) compared SMT to sham SMT/placebo, and four trials (435 participants) compared SMT to no treatment. Most trials (43, including 8291 participants) examined the effect of SMT compared to other conservative interventions. The remaining trials examined other comparisons.Treatment allocation was appropriately conducted in just four sham SMT/placebo‐controlled trials (24%), while only six trials ‘blinded’ participants to the intervention (35%), indicating a high risk of selection and performance bias. Similarly, the no‐treatment controlled trials were as susceptible to selection bias (50%) and performance bias (75%).Results

SMT versus sham SMT/placeboThe authors found very low‐certainty evidence (downgraded for inconsistency and study limitations) that SMT may result in a small reduction in pain compared to sham SMT/placebo at one month (mean difference (MD) ‐7.01, 95% confidence interval (CI) ‐12.48 to ‐1.53; I2 = 94%; 16 studies, 1570 participants) and very low‐certainty evidence (downgraded for study limitations and inconsistency) that SMT may result in a medium improvement in functional status compared to sham SMT/placebo at one month (standardised mean difference (SMD) ‐0.41, 95% CI ‐0.69 to ‐0.13; I2 = 82%; 13 studies, 1416 participants), but the evidence is very uncertain.SMT versus no treatment

The authors found very low‐certainty evidence (downgraded for study limitations, inconsistency, and imprecision) that SMT may result in a medium reduction in pain compared to no treatment at one month (MD ‐13.99, 95% CI ‐27.33 to ‐0.66; I2 = 89%; 4 studies, 325 participants), but the evidence is very uncertain. They found low‐certainty evidence (downgraded for study limitations and imprecision) that SMT may result in a large improvement in functional status compared to no treatment at one month (SMD ‐0.84, 95% CI ‐1.32 to ‐0.35; I2 = 71%; 4 studies, 312 participants).

SMT versus other conservative interventions

Low‐certainty evidence (downgraded for inconsistency) indicated that SMT may result in little to no difference in pain (MD ‐4.72, 95% CI ‐8.26 to ‐1.17; I2 = 89%; 31 studies, 4109 participants) and may result in a small improvement in functional status (SMD ‐0.25, 95% CI ‐0.38 to ‐0.11; I2 = 73%; 28 studies, 3940 participants) compared to other conservative interventions at one month.

These effects, however, should be interpreted with caution due to the substantial statistical heterogeneity for which there is no clear explanation.

Less than half of the studies (47%) reported on adverse events, of which 12 studies reported these systematically. Adverse events in the SMT group were limited to muscle soreness, stiffness, and/or transient increase in pain. None of the studies registered any serious complications related to either the experimental or control group treatment. The evidence is very uncertain about the adverse effects of SMT.

Authors’ conclusions: When SMT is compared to sham SMT/placebo, it may result in a small improvement in pain and medium improvement in functional status in adults with chronic low back pain. When compared to no treatment, SMT may result in a medium improvement in pain and a large improvement in functional status. When compared to other conservative interventions, SMT may result in little to no difference in pain and a small improvement in functional status. The evidence is of low to very low certainty, largely due to the fact that the effects of SMT were examined in trials conducted in different settings and populations, with different types of SMT technique, dosage, and frequency of treatment. Continuing to conduct RCTs in the same manner will neither strengthen the evidence nor our confidence in it.

Once again, it has been confirmed that most trials of SMT are, because of their failure to report adverse effects, in violation of ethical standards. But the importance of this excellent review lies elsewhere. Despite 76 published RCTs, there is huge uncertainty about the benefits of SAM. What should we make of this fact?

In my view, it highlights that:

  • the studies are often of poor quality;
  • the effect of SMT are so small that they are negligibel;
  • patients with back pain should look for treatments that are safe and effective;
  • the choice can therefore not be SMT.

3 Responses to Spinal manipulative therapy for adults with chronic low back pain, an update of a Cochrane Review

  • “SMT may result in a medium improvement in functional status compared to sham SMT/placebo at one month”

    “and may result in a small improvement in functional status compared to other conservative interventions at one month.”

    Compared to:

    “NSAIDs are slightly more effective than placebo regarding disability. However, the magnitude of the effects is small, and the level of evidence was low.”

    Non‐steroidal anti‐inflammatory drugs for chronic low back pain. Cochrane Database Syst Rev. 2016 Feb

    • whenever you quote selectively and compare to NSAIDs, you probably know yourself that you are bullshitting [unles, of course, you are more stupid than I thought].

  • Prof Ernst, this type of sarcastic reply to DC does you an injustice. In your position, with the status that you have acquired over the years, if you cannot be polite, don’t say anything at all.

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