10.4 Flashcards

(10 cards)

1
Q
  1. How is OA treatment approached in terms of structural pathology versus symptoms?
A

Current OA management divides treatment into addressing structural joint damage (though no approved disease–modifying drugs exist) and relieving symptoms like pain and disability.

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2
Q
  1. What are the key non-pharmacological treatments currently recommended for OA?
A

These include patient education, weight management, exercise (land-based and strength training), and self-management to improve function and reduce pain.

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3
Q
  1. What pharmacological treatments are used in OA management and what do they target?
A

Pharmacologic therapies—such as NSAIDs, paracetamol, and intra-articular corticosteroid or hyaluronic acid injections—primarily target pain and inflammation rather than reversing structural damage.

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4
Q
  1. What surgical options are available for severe OA?
A

Joint replacement (arthroplasty) is the main surgical intervention, though it is usually reserved for advanced disease after conservative treatments have failed.

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5
Q
  1. Why is there a gap in treatments that modify OA structure?
A

Current therapies focus on symptomatic relief because OA is a multifaceted, multi-tissue disease, and there are no approved drugs that reliably halt or reverse the underlying structural degeneration.

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6
Q
  1. What is the biological rationale behind developing future OA therapeutics?
A

Emerging treatments aim to target the underlying mechanobiological pathways that drive cartilage breakdown, synovial inflammation, and subchondral bone changes—often guided by OA phenotypes and specific biomarkers.

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7
Q
  1. How do mechanical and biological risk factors interact in OA pathogenesis?
A

Excessive loading, joint instability, adipokine secretion, and systemic inflammation all contribute to progressive tissue damage through complex cross-talk among cartilage, bone, and synovium.

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8
Q
  1. What are OA phenotypes and endotypes, and why are they important?
A

OA phenotypes are distinct subtypes based on variations in tissue involvement (e.g., cartilage-driven, synovitis-driven, bone-driven) that can guide personalized and targeted therapeutic strategies.

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9
Q
  1. How might biomarkers aid in developing new OA treatments?
A

Biomarkers help identify patient-specific disease endotypes, allowing clinicians to tailor interventions that target the active pathways driving degeneration and pain.

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10
Q
  1. What future directions are anticipated in OA management?
A

The field is moving toward multifaceted, phenotype-targeted therapies that address both structural changes and pain mechanisms, alongside improved risk factor modification and novel drug development.

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