Epicondylitis

About Epicondylitis

Epicondylitis, commonly referred to as “tennis elbow” (lateral epicondylitis) or “golfer’s elbow” (medial epicondylitis), is a common musculoskeletal condition affecting adults who engage in repetitive or sustained upper-limb activities. It is characterized by localized pain and tenderness at the lateral or medial epicondyle of the humerus and is frequently aggravated by gripping, lifting, or resisted wrist and forearm movements.

Epicondylitis is best understood as a load-related tendinopathy rather than an acute inflammatory condition. Its etiology is multifactorial and may involve repetitive mechanical loading, insufficient load tolerance of the tendon, suboptimal movement patterns, and inadequate conditioning of the forearm musculature. Symptoms often develop gradually and may fluctuate over time, influenced by activity demands, occupational exposures, and individual capacity to adapt to load.

About CCG Care Pathways

Purpose

CCG is a knowledge translation resource of the Canadian Chiropractic Association. Its care pathways help chiropractors and other clinicians organize conservative care for musculoskeletal conditions. Each pathway outlines the main steps of the clinical encounter and supports decisions about assessment, care, monitoring, referral, co-management, and discharge. The pathways provide a structured approach to care, not a fixed prescription.

Development

Pathways draw on relevant clinical practice guidelines, systematic reviews, peer-reviewed literature, and safety or professional sources. These sources inform, but do not determine, pathway content. Their findings reflect the questions, populations, outcomes, methods, and judgments used and may not apply to every person. Condition-specific sources are identified by author or organization and year, with full citations in one reference list at the end of the pathway.

Principles of Care

Musculoskeletal conditions are shaped by physical, psychological, social, cultural, and environmental factors, so no single approach fits everyone. Good care is ethical, evidence-informed, person-centred, culturally responsive, and tailored to the patient’s goals, preferences, circumstances, and response. Shared decision-making and informed consent guide care. Education, active rehabilitation, and self-management support recovery, functioning, participation, and long-term health. Regular reassessment shows whether the plan is helping and when to continue, adapt, stop, refer, co-manage, or discharge.populations.

Pathway Flow at a Glance

The pathway follows a recurring clinical cycle: understand the person and their goals; screen for safety and referral needs; develop a working clinical profile; agree on a plan and relevant outcomes; provide care; reassess response and safety; and continue, adapt, stop, refer, co-manage, or discharge as appropriate.

Disclaimer

CCG care pathways support professional clinical judgment; they do not replace it or the advice of a qualified provider. They are not prescriptive, authoritative, or regulatory and are not intended for diagnosis or billing. Clinicians remain responsible for practicing within their competence and scope, meeting applicable legal and regulatory requirements, obtaining informed consent, recognizing emergencies, and arranging referral or co-management when needed.

Epicondylitis Care Pathway

1. Record Keeping

Accurate, timely, and sufficiently detailed documentation supports safe, high-quality care. The record should reflect clinically relevant patient interactions, clinical reasoning, decisions, care provided, and progress over time. Documentation should meet the legal, regulatory, privacy, retention, and organizational requirements that apply where the clinician practices. A structured format, such as SOAP, may support consistency, clarity, and continuity and can be adapted to the encounter and practice setting.

Subjective: Record the patient’s concerns, symptoms, functioning and participation, goals, preferences, relevant history and context, and response or adverse effects from previous care.

Objective: Record relevant examination findings, outcome measures, diagnostic test results when available, and clinically important changes.

Assessment: Record the clinical interpretation of findings, working diagnosis or clinical profile, differential and safety considerations, relevant risk factors or modifiers, and the patient’s progress or response.

Plan: Record care provided or proposed, education and self-management, consent and patient decisions, changes to the plan, agreed outcomes and reassessment point, referrals or co-management, follow-up, and discharge planning.

Document at the time of the encounter or as soon as practicable. Corrections and additions should preserve the integrity of the record. Clear records support patient safety, shared decision-making, communication, continuity, and accountability.

2. Informed Consent
  • Definition: A continuing process in which a capable patient, or an authorized substitute decision-maker when required, voluntarily agrees to a proposed examination or intervention after receiving and understanding the information needed to make an informed choice.
  • Key Aspects:
    • Prior to interaction: Obtain consent before beginning an examination, procedure, or treatment, except where applicable law permits otherwise. Explain what is proposed and why. Revisit consent when the plan or material information changes.
    • Voluntarily and specific: must be voluntary and specific to the proposed care. Consider the patient’s capacity for the decision at the time it is required and follow applicable requirements for substitute decision-making when the patient lacks capacity. The patient may ask questions, refuse, place limits on, or withdraw consent.
    • Transparent process: Use honest, plain, and accessible communication. Offer interpretation or other communication support when needed and consider language, culture, health literacy, disability, and prior trauma. Written or digital information may support but does not replace discussion.
    • Patient understanding and agreement:
      • Diagnosis/prognosis: Explain relevant findings, the clinical impression or working diagnosis, important uncertainty, and the expected course in understandable language.
      • Treatment plan: Discuss the nature and purpose of proposed care, expected benefits, material risks and side effects, burdens, reasonable alternatives, the option of no intervention, and the likely consequences of accepting or declining.
      • Questions: Invite questions, explore goals and preferences, allow appropriate time for a decision, and confirm understanding, for example using teach-back.
    • Documentation: Record the consent discussion and decision, including material information provided, questions, capacity or substitute decision-maker where relevant, consent, refusal, limits or withdrawal, and any need to revisit consent. Follow documentation requirements applicable to the jurisdiction and practice setting.
3. Health History
  • Apply cultural awareness and trauma-informed care principles.
  • Sociodemographic information: Age, gender, sex, race/ethnicity.
  • Main complaint: Location of elbow pain (medial or lateral), onset (gradual or sudden), duration, severity, and symptom behaviour. Identify aggravating and easing factors (e.g., gripping, lifting, repetitive wrist or forearm use).
  • Body systems: Neurologic, cardiovascular, genitourinary, gastrointestinal, musculoskeletal, bone density, eyes/ears/nose/throat, respiratory, skin, mental health, reproductive.
  • Health, lifestyle, and history: Past medical conditions, medications (including opioids, anticoagulants, corticosteroids etc.), supplements, injuries, comorbidities, hospitalizations, surgeries, diet, exercise, sleep habits, smoking, alcohol/substance use, family support, caregiver responsibilities, work/school environment.
  • Work, sport, and activity exposure: Occupational demands, repetitive tasks, forceful gripping, sustained postures, tool use, sports or recreational activities, recent changes in workload or technique, and hand dominance.
  • Social determinants of health: Employment, childcare, education, nutrition, housing, domestic violence, child maltreatment, discrimination, social isolation.
  • Previous care and responses: Prior treatments (e.g., exercise, manual therapy, injections, bracing, medication), perceived benefit, adverse effects, and adherence.
  • Beliefs, expectations, and understanding: Understanding of their condition, expectations of care, concerns about prognosis, work participation, or long-term impact.
  • Screen for flags: Identify red flags, orange flags, and psychosocial (yellow) factors that may influence care planning.

​​Outcomes Assessments:

  • Pain: Use pain scales (e.g., NRS) and diagrams.
  • Function and Participation: Evaluate impact on daily activities (PSFS, WHODAS, PRTEE, QuickDASH).
  • Recovery: Use self-rated recovery scales.
  • Quality of life: Assess using tools such as SF-12.
  • Work/school status: Monitor return to activities.
  • Individual goals: Set SMART goals (Specific, Measurable, Achievable, Relevant, Timely).
  • Patient feedback: Gatherand integrate patient experience and satisfaction.
4. Red Flags : Differential Diagnosis Requiring Medical Referral

ACTION: Refer immediately to emergency care:

  • Acute traumatic injury: Suspected fracture or dislocation following trauma, marked deformity, significant swelling, inability to move the elbow, or severe pain.
  • Suspected septic process: Rapid onset of swelling, erythema, warmth, fever, or systemic symptoms suggestive of septic olecranon bursitis or joint infection.
  • Neurovascular compromise: Progressive neurologic deficits, loss of distal pulses, or signs of compartment syndrome.

ACTION: Refer to appropriate medical provider:

  • Inflammatory or systemic disease: Suspicion of inflammatory arthritis (e.g., rheumatoid arthritis, gout) based on multi-joint involvement, morning stiffness, or systemic features.
  • Ligamentous injury or instability: Suspected ulnar collateral ligament injury, particularly in throwing athletes or following acute valgus stress.
  • Intra-articular pathology: Locking, catching, or inability to fully extend or flex the elbow suggestive of osteochondral defects or loose bodies.
  • Persistent or worsening symptoms: Progressive pain, swelling, or functional loss that is disproportionate to findings or not responding to appropriate conservative care.
5. Orange Flags: Symptoms of Psychiatric Disorders Requiring Referral

Orange Flags are signs that a mental health or substance use concern may require emergency or timely assessment or shared care, and may change whether and how MSK care proceeds. They are not diagnoses. Ask directly and respectfully when concern arises, considering immediate safety, severity, change from usual, daily functioning and context. Psychosocial factors that may affect recovery but do not require separate mental health or medical assessment are addressed under Yellow Flags.

ACTION: Arrange emergency assessment now when there is immediate danger or an urgent medical need:

  • Suicide, self-harm or harm to others: current intent or plan, a recent attempt, inability to stay safe, or behaviour suggesting an immediate risk of serious harm.
  • Severe change in mental state: extreme agitation, confusion, disorganization, possible psychosis or mania with impaired judgment or unsafe behaviour, or inability to meet basic needs when this creates immediate danger.
  • Substance-related or medical emergency: suspected overdose, severe intoxication, dangerous withdrawal, delirium or another sudden change requiring urgent medical care.

When immediate safety is uncertain, do not leave the person alone while help is arranged. Follow local emergency procedures and call 9-1-1 for immediate danger or urgent medical need. If the person is thinking about suicide, call or text 9-8-8: Suicide Crisis Helpline with them or support them to do so.

If violence, abuse or exploitation is disclosed or suspected, support immediate safety and follow applicable safety and reporting requirements.

ACTION: Arrange prompt medical or mental health assessment when there is:

  • Suicide or self-harm thoughts: thoughts without immediate danger.
  • Substantial symptoms or effects: severe, persistent or worsening symptoms of depression, anxiety, trauma, possible psychosis or mania, eating problems or substance use that substantially affect daily life, decision-making or safe participation in care.
  • Other reasons for assessment: a marked change from usual behaviour or functioning; concern about medication or substance effects; a presentation outside the clinician’s competence; or a request for help.

Agree with the patient on who will be contacted, how soon and what to do if the situation worsens. Confirm that the person has connected with the service when clinically important.

ACTION: Adapt and coordinate MSK care:

  • Safe care: care may continue when it is safe and acceptable and does not delay needed assessment. Adapt communication, examination and care; obtain ongoing consent; and coordinate with other providers with the patient’s permission.
  • Continue the MSK assessment: do not assume that a mental health or substance use concern explains the MSK presentation. Continue to consider physical causes and the patient’s account.
  • Questionnaires: they may support conversation and monitoring, but do not establish a diagnosis or replace direct questions, clinical judgment or action.
  • Acceptable support: ask what type of help is acceptable and whether language, cultural, family, community or other supports are important to the patient.

ACTION: Document and follow up:

Record the concern; relevant questions and the patient’s responses; the safety decision and reasons; actions, advice and referrals; communication and consent; follow-up; and any unresolved concern. Follow applicable privacy, safety and reporting requirements.

For provincial, territorial and national services, see Mental health support: Get help (Public Health Agency of Canada 2026).

6. Yellow Flags: Factors that May Affect Recovery or Participation

Yellow Flags are personal, social, work, school, healthcare, environmental or structural factors that may influence symptoms, functioning, participation or response to care. They are contextual, not diagnoses or certain predictions, and do not mean that symptoms are psychological. They guide how care is tailored and do not by themselves require urgent referral. Explore them through conversation and ongoing outcome review, with attention to the patient’s priorities, strengths and circumstances. A separate Yellow Flag score is not required. New or worsening signs of serious physical illness follow the Red Flag process. Mental health or substance use concerns that need separate assessment, or any immediate safety concern, follow the Orange Flag process and applicable emergency or safeguarding procedures.

Explore relevant factors:

  • Understanding, expectations and healthcare experiences: concerns about injury or damage, uncertainty, recovery expectations, confidence, conflicting advice, previous dismissal or harm, and trust in care.
  • Responses to symptoms and activity: worry, fear, avoidance, cycles of doing too much and then needing prolonged rest, difficulty pacing, coping, sleep, confidence in self-management, and return to meaningful activities.
  • Emotional and life context: distress, low mood, anxiety, grief, trauma, caregiving, relationship change, job loss or other major events. Ask permission before sensitive questions and limit discussion to what is relevant and acceptable to the patient.
  • Relationships, culture and strengths: supportive relationships, isolation, family and community roles, cultural or spiritual practices, identity, preferences, language and other sources of resilience.
  • Work, school and administrative context: physical and psychosocial demands, control, satisfaction, job security, accommodations, return concerns, and compensation, insurance or legal processes. Explore these neutrally and in context.
  • Social and structural conditions: consider social and structural determinants of health (Public Health Agency of Canada 2026), including income, housing, food security, transportation, childcare, access and cost of care, discrimination, racism, colonialism, neighbourhood and workplace conditions, and physical or digital accessibility.

ACTION: Respond with the patient:

  • Ask, do not assume: use open questions to understand what helps, what gets in the way, what matters and what feels feasible. Ask about strengths and protective factors, not only difficulties. Do not treat a person’s circumstances, culture or choices as a deficit.
  • Plan together: integrate relevant findings into shared goals, education, self-management, physical activity or exercise, and participation in meaningful activities. Adapt communication, setting, pace, cost and access where possible.
  • Connect and coordinate: with the patient’s consent, consider appropriate clinical, social, workplace, school, community, Indigenous or culturally specific supports. Clarify who will do what and follow up when the connection is important to the plan.
  • Review response to care: reassess the patient’s account and the pathway’s selected outcomes at clinically relevant points. If progress differs from expected, review the clinical impression, care plan, access and other barriers; do not automatically attribute the outcome to Yellow Flags.
  • Document: record relevant factors and strengths, the patient’s priorities and preferences, agreed actions, consent, referrals or coordination, follow-up, and any change requiring the Orange Flag process.
7. Physical Examination

The physical examination should be focused, hypothesis-driven, and informed by the health history and identified risk factors.

  • Observation: Inspect the upper limb for asymmetry, swelling, discoloration, muscle wasting, or protective postures. Observe functional movements involving gripping, lifting, or forearm rotation.
  • Range of motion (ROM): Assess active, passive, and resisted wrist, elbow, and shoulder ROM. Note pain reproduction, movement limitations, or compensatory patterns.
  • Palpation: Palpate the lateral and medial epicondyles and surrounding soft tissues for localized tenderness, thickening, temperature changes, or swelling. Assess adjacent regions (forearm, wrist, shoulder) as clinically indicated.
  • Grip strength: Evaluate grip strength and pain response during gripping tasks, particularly in functional or provocative positions.
  • Neurological examination: Perform a focused neurologic examination if symptoms suggest neural involvement, including assessment of sensation, reflexes, and myotomes. Consider screening for cubital tunnel syndrome or radial tunnel syndrome when indicated.
  • Special/Orthopedic Tests: Use condition-specific tests selectively to support clinical reasoning (e.g., pain reproduction with resisted wrist extension for lateral symptoms or resisted wrist flexion for medial symptoms).
  • Advanced Diagnostics: Imaging is not routinely indicated for suspected epicondylitis. Radiography may be considered in cases of trauma, suspected fracture, or atypical presentation. Advanced imaging should be reserved for refractory cases or when alternative pathology is suspected.

8. Clinical Presentation for Epicondylitis

Epicondylitis typically presents as localized, activity-related elbow pain that is mechanically provoked.

Common features include:

  • Reduced tolerance to load rather than constant pain at rest.
  • Pain localized to the lateral or medial elbow, aggravated by gripping, lifting, or repetitive wrist and forearm movements.
  • Functional difficulty with everyday tasks (e.g., opening jars, carrying objects, tool use, work- or sport-specific activities).

Presentation may vary by symptom location:

Lateral elbow presentations may include:

  • Lateral elbow pain with decreased strength or pain during resisted gripping.
  • Pain reproduced with resisted wrist extension.
  • Pain at the lateral elbow with isolated resisted extension of the middle finger.

Medial elbow presentations may include:

  • Medial elbow pain aggravated by resisted wrist flexion and forearm pronation.

Additional considerations:

  • Localized tenderness near the epicondyle is common.
  • Functional limitations may reflect compensatory movement patterns or concurrent impairments at the wrist, shoulder, or cervical region.
  • Symptom impact and care-seeking behaviour may be influenced by occupational demands, psychosocial factors, and prior experiences with care.
9. Conservative Treatment Considerations for Epicondylitis

Conservative Treatment Considerations for Epicondylitis (Lucado 2022, Hoogvliet 2013)

Management should be individualized, multimodal, and focused on improving load tolerance, function, and participation. No single intervention is universally effective. 

Applies to both lateral epicondylitis (LE) and medial epicondylitis (ME)

  • Education/self-management: activity modification, pacing, graded return to valued activities, and aligning expectations with a load-related tendinopathy framework. 
  • Therapeutic exercise: progressive, symptom-guided loading of the involved musculature (isometric, concentric, and/or eccentric). 
  • Multimodal care: combine exercise with other conservative interventions as clinically indicated (e.g., manual therapy, taping, supports). 

Lateral epicondylitis (LE)

  • Manual therapy (local and regional): elbow mobilization/manipulation to reduce pain and improve pain-free grip strength; regional techniques (cervical/thoracic/wrist) as adjuncts when impairments are identified. 
  • Soft tissue interventions: may be used as adjuncts within a multimodal plan (particularly when paired with exercise). 
  • Adjuncts for short-term symptom relief: taping, TENS/cryotherapy/laser where appropriate, recognizing that benefits may be short-term. 
  • Dry needling: may be considered for pain/function as part of a broader plan (evidence varies by technique and comparator). 

Medial epicondylitis (ME)

  • Exercise: progressive loading of the wrist flexor–pronator group. 
  • Screen and account for ulnar nerve involvement: ulnar neuritis can co-occur and should inform treatment and referral/co-management decisions. 

Adjuncts: consider bracing/supports and other modalities selectively based on symptom response and functional demands (not as stand-alone care).

10. Risk and Prognosis for Epicondylitis

Common Risk Factors (Lucado et al., 2022):

  • Repetitive or sustained wrist bending/twisting and forearm rotation (e.g., screwing, tool use).
  • High perceived physical exertion combined with elbow flexion/extension and wrist bending, particularly when performed for more than 2 hours per day.
  • Repetitive hand or wrist movements for at least 2 hours per day, especially among individuals with long-term exposure (e.g., ≥9 years).
  • Occupational tasks involving handling loads greater than 20 kg at least 10 times per day over prolonged periods (e.g., >20 years).
  • Individual factors including female sex, dominant-side involvement, previous smoking history, and co-existing upper-limb conditions (e.g., rotator cuff disorders, De Quervain’s disease, carpal tunnel syndrome).
  • Low job control and low social support.

Prognosis (Lucado et al., 2022):

  • The clinical course is influenced by the degree to which ongoing activity demands continue to exceed tissue load tolerance.
  • Some individuals experience full and timely symptom resolution with conservative, non-surgical care.
  • However, more than half of individuals seeking general medical care continue to report symptoms at one year.
  • Approximately 20% of individuals report persistent pain lasting 3–5 years following care.
11. Ongoing Follow-up

Ongoing follow-up is a shared review of whether the plan remains safe, useful, acceptable and aligned with the patient’s goals. The timing of review should reflect symptoms, risk, the care being tried, goals and access rather than a fixed visit schedule.

  • Review symptoms and safety: ask what has changed in symptoms, functioning and daily activities; review adverse effects; and check for new or worsening Red Flags and relevant Orange or Yellow Flag concerns. Arrange earlier or urgent assessment when the findings require it.
  • Review outcomes: repeat the small set chosen at baseline and use the same measures when possible. These may include the Patient-Specific Functional Scale, WHODAS 2.0, quality of life using the patient’s own rating or a measure such as WHOQOL-BREF, symptom impact, participation and the patient’s own assessment of change. Interpret measures with the patient and alongside what has changed in daily life rather than relying on a score alone.
  • Review goals, preferences and consent: ask whether care remains acceptable, feasible and worthwhile; revisit goals and priorities; and confirm consent when the plan or circumstances change.
  • Adapt care: continue what is useful and acceptable, and change, pause or stop what is not. If progress is not sufficient from the patient’s perspective, review the clinical impression, the fit and amount of care, barriers to participation, other health or social factors and whether other expertise is needed.
  • Support self-management and participation: review the strategies the patient is using, including physical activity or exercise, symptom management, pacing and participation in work, school, caregiving, recreation or community life. Ask what is helping and which barriers can be addressed.
  • Referral and co-management: arrange emergency assessment for Red Flags requiring urgent care. Consider referral or co-management when findings or needs are beyond the clinician’s role, the patient’s condition is worsening, progress remains insufficient after the plan has been reviewed, or the patient requests another opinion.
  • Plan the next step: agree whether to continue, change the interval between visits, move toward more self-directed care, or apply the Criteria for Discharge section.
12. Criteria for Discharge

Discharge is a shared decision about ending or transferring a course of care. It does not require complete symptom resolution, a normal outcome score or a fixed number of visits.

  • When discharge may be appropriate: consider discharge when the patient’s goals have been met to a degree they consider satisfactory; the patient feels able to manage with less or no clinician involvement; the patient chooses to end care; continued care is not providing enough benefit to justify its burden, cost or time; or care is being transferred to another provider.
  • Reassess before discharge: review symptoms, functioning, participation, selected outcomes, goals, adverse effects, confidence and preferences. Check for new or worsening Red Flags and any Orange or Yellow Flag concerns that still require action. If the condition is worsening or a safety concern remains, arrange the required assessment or referral rather than routine discharge.
  • When progress has slowed: review the clinical impression, response to care, goals, barriers and access, other health or social factors, and other reasonable options before deciding with the patient whether to continue, change or end care.
  • Plan after discharge: agree on self-management, physical activity or exercise, symptom management, pacing and participation in work, school, caregiving, recreation or community life. Explain which changes should prompt earlier or urgent assessment and when and where to seek care.
  • Future access to care: explain how the patient can return if symptoms recur, functioning declines, or goals or demands change. Any planned future review or supportive care should have an agreed purpose, expected benefit and review point.
  • Referral or transfer: explain the reason, share a relevant summary with the patient’s consent, and clarify who will address outstanding concerns when possible. Avoid an unintended gap in care when safety or ongoing needs remain.
  • If the patient ends care or does not return: respect the patient’s right to stop. Record what is known and unknown about the outcome, advice or referral offered, attempts to communicate when clinically warranted, and any unresolved safety concern. Follow applicable record keeping and communication requirements.
  • Documentation: record the reason care ended, the patient’s status and selected outcomes, goals and preferences, unresolved concerns, advice and self-management plan, referral or transfer details, and how to seek care again if needed.