Background
Low back pain (LBP) is a leading cause of disability worldwide1, yet the majority of cases are classified as “non-specific”, lacking a clearly defined pathophysiological basis2. Mechanistic phenotyping offers a promising framework by distinguishing nociceptive (NoP), neuropathic (NeP), and nociplastic (NcplP) pain mechanisms3. Recent literature increasingly recognises a substantial subset of patients with mixed pain (MixP) – those exhibiting overlapping features of NoP, NeP, and NcplP – yet clinical understanding of this phenotype remains limited4,5.
Existing evidence suggests MixP is prevalent, yet underdiagnosed, and associated with greater symptom severity, functional impairment, and psychological burden compared to singular pain phenotypes6.
Objective
The study explores the evolving conceptualisation of MixP in LBP, with a focus on its clinical and cognitive correlates. The study seeks to evaluate the associations between MixP (as classified by the painDETECT questionnaire) and outcomes including pain intensity, disability, quality of life, and cognitive-emotional factors.
A retrospective analysis of a prospectively collected tertiary clinic database will be conducted, incorporating patient-reported outcomes (NRS, EQ-5D, ODI, modified NASS-LS) and radiographic data. The study aims to clarify the symptom burden of MixP relative to NoP and NeP groups, and to assess whether mixed mechanisms predict poorer clinical outcomes. Though data collection is ongoing, preliminary trends indicate notable differences between pain phenotypes in pain quality and the presence of pain beyond the low back region. Findings are anticipated to inform more targeted and mechanism-based approaches to LBP management and to address a key gap in current phenotyping models.