| Literature DB >> 36195914 |
Annelieke Cesanne Moorman1,2, David Newell3.
Abstract
OBJECTIVES: An audible pop is the sound that can derive from an adjustment in spinal manipulative therapy and is often seen as an indicator of a successful treatment. A review conducted in 1998 concluded that there was little scientific evidence to support any therapeutic benefit derived from the audible pop. Since then, research methods have evolved considerably creating opportunities for new evidence to emerge. It was therefore timely to review the evidence.Entities:
Keywords: Audible pop; Chiropractic; Pain; Spinal manipulation; Systematic review
Mesh:
Year: 2022 PMID: 36195914 PMCID: PMC9531394 DOI: 10.1186/s12998-022-00454-0
Source DB: PubMed Journal: Chiropr Man Therap ISSN: 2045-709X
Fig. 1PRISMA flow diagram
Study characteristics
| Study | Aim | Participants | Intervention | Presence of AP’S | Outcome measure | Conclusion |
|---|---|---|---|---|---|---|
Bialosky et al. [ U.S.A Prospective Cohort Secondary analysis | Assess the role of the AP in HVLA manipulation associated thermal pain sensitivity to both A-delta fiber mediated pain perception and temporal summation | n = 40 Males and females, pain free, aged 18–60 | HVLA thrust technique on the sacroiliac joint two times on each side, regardless of whether an AP was perceived. The examiner noted if AP was perceived | AP present: n = 18 AP absent: n = 22 | NPRS as a measure of expected and perceived pain and psychological questionnaires (PCS, FPQ-III and anxiety VAS). Immediate follow-up directly after intervention and after 4 min | Hypoalgesia is associated with HVLA manipulation and occurs independently of a perceived AP. Inhibition of lower extremity temporal summation may be larger when AP is perceived |
Sillevis and Cleland [ U.S.A RCT secondary analysis | 1. Determine if audible sounds during a thrust manipulation have an immediate effect on pain perception within a group of chronic neck pain patients. 2. Determine if there is a positive correlation between the presence of audible sounds and a change in autonomic function | n = 100 Males and females with chronic (present for at least 3 months) cervical pain aged 18–65 | High-velocity anterior-to-posterior force to the upper thoracic spine targeting T3-T4 segment in supine position. Presence of audible sounds recorded by the researcher. Control: mobilization directed at T3-T4 | n = 50 mobilization n = 50 manipulation of which One pop: n = 14 Multiple pops: n = 18 No pop: n = 18 | VAS used to assess pain and automated pupillometry used to capture pupil responsiveness measured in the form of pupil diameter. Follow-up directly after intervention and after 4 min | The presence of joint sounds does not influence the overall activity of the autonomic nervous system (P = .31, .44, .47, respectively) following a thrust manipulation or contribute to the reduction of pain (P > 0.05) in patients with chronic neck pain |
Cleland et al. [ U.S.A Prospective Cohort secondary analysis | Examine the relationship between the audible pop and patient-centered outcomes in a cohort of patients with neck pain treated with thoracic spine thrust manipulation | n = 72 Males and females with neck pain with or without unilateral upper extremity symptoms, and baseline NDI > 10% aged 18–60 | 3 different thrust manipulation techniques to the thoracic spine: distraction manipulation, upper and middle thoracic spine manipulation. The presence or absence of an AP was noted by the treating therapist. 3 thrusts were repeated if no AP was noted | ≤ 3 pops: n = 21 > 3 pops: n = 51 | Change scores for pain and disability (NDI and NPRS) and cervical ROM. Additionally, GROC was completed. Follow-up 2–4 days after first session | No relationship between the number of audible pops and clinically meaningful improvements in pain (P = 0.41), disability (P = 0.66) or cervical ROM (P > 0.05) in patients with neck pain |
Flynn et al. [ U.S.A Prospective Cohort secondary analysis | Investigate whether the occurrence of a manipulative pop during sacroiliac region manipulation is related to the outcome of the intervention over a 4-week period | n = 70 Males and females with a primary complaint of low back pain with or without referral into the lower extremity and an ODQ score of > 30% aged 18–60 | Total of 5 physical therapy sessions over 4 weeks. In the first two sessions pts received HVLA thrust manipulation on the sacroiliac region on the more symptomatic side, and ROM exercise. If cavitation heard onto ROM exercise. If no cavitation heard after additional attempt on opposite side with a maximum of two attempts per side, onto ROM exercise. Cavitation was noted by the patient or therapist | AP present: n = 59 AP absent: n = 11 | NPRS to rate pain intensity, ODQ and measurement of lumbopelvic flexion ROM changes. Follow-up at 1 week, and 4 weeks after intervention | AP may not relate to improved outcomes from HVLA thrust manipulation for patients with non-radicular low back pain at either an immediate odds ratio: 1.1 (95% CI, 0.29–3.86) or longer-term odds ratio: 1.7 (95% CI, 0.41–7.1) follow-up |
Flynn et al. [ U.S.A Prospective Cohort | Investigate whether the occurrence of a manipulative pop during sacroiliac region manipulation is related to the outcome of the intervention | n = 71 Males and females with non-radicular low back pain aged 18–60 | HVLA thrust technique on the sacroiliac joint, side determined by an algorithm. The therapist noted whether the therapist or patient heard an AP. If no AP, the manipulation was repeated. If no AP, the therapist manipulated the opposite site with a maximum of 2 attempts per side | AP present: n = 50 AP absent: n = 21 | Changes in ROM, NPRS scores and modified ODQ scores. Reassessment 48 h after the manipulation | No relationship between AP during sacroiliac region manipulation and improvement in ROM (P = 0.74), pain (P = 0.23) or disability (0.49). Occurrence of AP did not improve odds of dramatic improvement |
AP Audible Pop, HVLA High-Velocity Low-Amplitude, NPRS Numeric Pain Rating Scale, PCS Pain Catastrophizing Scale, FPQ-III Fear of Pain Questionnaire III, VAS Visual Analog Scale, RCT Randomized Controlled Trial, NDI Neck Disability Index, ROM Range of Motion, GROC Global Rating of Change, ODQ Oswestry Disability Questionnaire.
Evaluation of Bias
| Bialosky (2010) | Cleland (2007) | Flynn (2003) | Flynn (2006) | Sillevis (2011) | ||
|---|---|---|---|---|---|---|
| Q1 | Hypothesis/aim/objective clearly described | 1 | 1 | 1 | 1 | 1 |
| Q2 | Main outcomes in Introduction or Methods | 1 | 1 | 1 | 1 | 1 |
| Q3 | Patient characheristics clearly described | 1 | 1 | 1 | 1 | 1 |
| Q4 | Interventions of interest clearly described | 1 | 1 | 1 | 1 | 1 |
| Q5 | Principal confounders clearly described | 2 | 1 | 1 | 1 | 1 |
| Q6 | Main findings clearly described | 1 | 1 | 1 | 1 | 1 |
| Q7 | Estimates of random variability provided for main outcomes | 1 | 1 | 1 | 1 | 1 |
| Q8 | All adverse events of interventon reported | 0 | 0 | 0 | 0 | 0 |
| Q9 | Characteristics of patients lost to follow-up described | 0 | 1 | 1 | 1 | 1 |
| Q10 | Probability values reported for main outcomes | 1 | 1 | 1 | 1 | 1 |
| Q11 | Subjects asked to participate were representive of source population | 1 | 1 | 1 | 1 | 1 |
| Q12 | Subjects prepared to participate were representive of source population | 1 | 1 | 1 | 1 | 1 |
| Q13 | Location and delivery of study treatment was representative of source population | UTD | UTD | UTD | UTD | UTD |
| Q14 | Study participants blinded to treatment | 0 | 0 | 0 | 0 | 0 |
| Q15 | Blinded outcome assessment | 0 | 0 | 0 | 0 | 0 |
| Q16 | Any data dredging clearly described | 1 | 1 | 1 | 1 | 1 |
| Q17 | Analyses adjust for differing lenths of follow-up | 1 | 1 | 1 | 1 | 1 |
| Q18 | Appropriate statistical tests performed | 1 | 1 | 1 | 1 | 1 |
| Q19 | Compliance with interventions was reliable | 1 | 1 | 1 | 1 | 1 |
| Q20 | Outcome measures were reliable and valid | 1 | 1 | 1 | 1 | 1 |
| Q21 | All participants recruited from the same source population | 1 | 1 | 1 | 1 | 1 |
| Q22 | All participants recruited over the same time period | 1 | 1 | 1 | 1 | 1 |
| Q23 | Participants randomized to treatment(s) | 0 | 0 | 0 | 0 | 1 |
| Q24 | Allocation of treatment concealed from investigators and participants | 0 | 0 | 0 | 0 | 1 |
| Q25 | Adequate adjustment for confounding | UTD | UTD | UTD | UTD | UTD |
| Q26 | Losses to follow-up taken into account | 1 | UTD | UTD | UTD | 1 |
| Q27 | Sufficient power to detect treatment effect at significance level of 0.05 | UTD | UTD | UTD | UTD | 1 |
| Total | 20 | 18 | 18 | 18 | 22 | |
UTD Unable to determine