Myalgia
OtherOverview
Myalgia refers to muscle pain that may be localised to a specific region or widespread across multiple body areas. It is a symptom rather than a standalone diagnosis, arising from a broad range of causes including mechanical overload, systemic illness, inflammatory conditions, medications, and psychosocial factors. Accurate clinical assessment is essential to identify the underlying aetiology and guide appropriate management or referral.
Pathophysiology
Muscle pain arises through nociceptive activation of free nerve endings within muscle tissue, triggered by mechanical stress, metabolic byproducts (e.g. lactate, bradykinin, prostaglandins), ischaemia, or inflammatory mediators. Central sensitisation may amplify pain perception in chronic or widespread presentations. The underlying cause determines the dominant mechanism — peripheral sensitisation in localised overuse injury, immune-mediated inflammation in viral or autoimmune myalgia, and altered descending inhibition in fibromyalgia-spectrum disorders.
Patient Education
Muscle pain is common and usually resolves with rest, gentle movement, and time. Staying active within comfortable limits, maintaining hydration, and addressing sleep and stress are important for recovery. If pain is widespread, persistent, or accompanied by other symptoms such as fatigue, fever, or weakness, further assessment is recommended.
Typical Presentation
Site
Localised (single muscle or region) or diffuse/widespread (multiple regions)
Quality
Deep aching, heaviness, tenderness to touch; may be sharp with acute injury or burning in neuropathic overlap
Intensity
Variable; 2–8/10 depending on aetiology and acuity
Aggravating
Physical activity, sustained postures, palpation, psychological stress, poor sleep, cold environments
Relieving
Rest, heat, gentle movement, analgesia, improved sleep, hydration
Associated
Fatigue, reduced range of motion, muscle stiffness, weakness; systemic features (fever, malaise) if infective or inflammatory cause
Orthopaedic Tests
Palpation of Affected Muscle Groups
Procedure
Systematic palpation of symptomatic muscle regions; assess for tenderness, trigger points, guarding, or swelling
Positive Finding
Reproducible tenderness or pain consistent with patient's complaint
Sensitivity / Specificity
Unknown / Unknown
Interpretation
Confirms localisation of pain; helps identify trigger points or regional vs widespread distribution
Resisted Muscle Testing (Regional)
Procedure
Apply resistance to the affected muscle group through its range; assess for pain and/or weakness
Positive Finding
Pain with resistance (contractile tissue involvement) or weakness suggesting muscle pathology or neurological involvement
Sensitivity / Specificity
Unknown / Unknown
Interpretation
Differentiates contractile vs inert tissue involvement; weakness may indicate myopathy, nerve involvement, or pain inhibition
Functional Movement Screen (e.g. Squat, Single-Leg Stance)
Procedure
Observe patient performing basic loaded or unloaded movements relevant to their complaint
Positive Finding
Pain reproduction, compensatory patterns, or inability to complete movement
Sensitivity / Specificity
Unknown / Unknown
Interpretation
Assesses functional impact and movement quality; guides exercise prescription and identifies contributing biomechanical factors
⚠ Red Flags
- •Severe proximal muscle weakness with elevated CK suggesting inflammatory myopathy (polymyositis, dermatomyositis)
- •Myalgia with fever, rash, or systemic illness suggesting viral or bacterial infection (e.g. Ross River virus, influenza, sepsis)
- •Dark urine with acute severe myalgia suggesting rhabdomyolysis — urgent medical referral
- •New myalgia in patient on statins or other myotoxic medications suggesting drug-induced myopathy
- •Unintentional weight loss, night sweats, or fatigue suggesting malignancy or systemic inflammatory disease
- •Temporal arteritis pattern (jaw claudication, scalp tenderness, visual changes) in older adults with new head/neck myalgia
⚡ Yellow Flags
- •Widespread pain with fatigue, sleep disturbance, and cognitive symptoms suggesting fibromyalgia-spectrum disorder
- •High pain catastrophising or fear-avoidance beliefs amplifying symptom reporting
- •Significant psychosocial stressors, anxiety, or depression concurrent with onset
- •Prolonged symptom duration without clear structural cause suggesting central sensitisation
- •Frequent healthcare seeking across multiple providers without diagnosis
Osteopathic Techniques
Region
Symptomatic muscle group
Technique
Soft Tissue
Rationale
Direct inhibition and myofascial release reduce peripheral nociceptive input, address trigger points, and restore local tissue extensibility
Region
Cervical/thoracic/lumbar spine (as relevant)
Technique
Articulation
Rationale
Restores segmental mobility and reduces referred muscular tension from restricted spinal segments; addresses neuromotor contributors to regional myalgia
Region
Affected musculature
Technique
MET
Rationale
Muscle energy techniques restore resting muscle length, improve proprioceptive input, and reduce protective guarding around painful regions
Region
Rib cage and thoracic spine
Technique
Soft Tissue / Articulation
Rationale
Improves respiratory mechanics and autonomic tone; addresses widespread myalgia with a postural or respiratory component
Add-On Approaches
Chinese Medicine
Acupuncture to local ashi points and distal points for pain modulation; cupping for localised muscle tension
Chiropractic
Spinal manipulation for segmental contributors; soft tissue adjuncts; ergonomic and activity advice
Physiotherapy
Graded exercise therapy, hydrotherapy, pain neuroscience education, sleep hygiene, activity pacing
Remedial Massage
Trigger point therapy, myofascial release, lymphatic techniques for inflammatory myalgia
Rehabilitation Exercises
Gentle Walking / Low-Impact Cardiovascular
Diaphragmatic Breathing and Relaxation
Progressive Muscle Relaxation Stretching
Graded Resistance Training — Region-Specific
Referral Criteria
- •Suspected rhabdomyolysis (dark urine, severe weakness, acute onset) — emergency referral
- •Elevated CK with progressive proximal weakness — rheumatology or neurology referral for inflammatory myopathy workup
- •Myalgia in context of systemic illness, fever, or rash — GP/medical referral for infectious or inflammatory workup
- •Suspected statin or drug-induced myopathy — GP referral for medication review
- •Widespread pain meeting fibromyalgia criteria unresponsive to conservative care — pain specialist or rheumatology referral
- •Persistent unexplained myalgia >6–8 weeks without improvement — GP referral for bloods (CK, ESR, CRP, TFTs, FBC)
Consider These Diagnoses
This presentation may reflect several distinct diagnoses. Use the links below to explore conditions that may better explain the clinical picture.