Lecture 25 Flashcards
(8 cards)
Mechanisms
active process where cells in joint tissues repond to external stimuli and drives structural pathologies. External signals can be mechanical or biological and can affect different tissues. As they communicate with each other, all tissues are impacted and cascade begins.
Modifiable risk factors
Obesity and joint injury can activate multiple signalling pathways that drives joint OA and pain onset/progression.
Pathology vs pain
targeting one tissue does not treat pathology in another. Disability and physical problems are clinical issues that may or may not be correlated with pain. Pain is not correlated with structural disease and treatments may not help with pain. Also, different types of pain have different molecular drivers and treatment targets. No structurally modifying drugs approved that reverse, halt or slow OA. Now, key targets is symptom management and decrease risk factors
symptom and risk factor management
Holistic evaluation of patients and conditions. Focus on clinical not imaging diagnosis to develop plan based of patient needs and wants. Some patients should also not have treatments
comorbidities
accompanied by heart disease, hypertension, depression and diabetes, increase management complexity. Treatment of OA mustn’t worsen comorbidity. Topical and oral non-steroidal anti inflammatory drugs are recommended as 1st line of treatment, decrease paracetamol due to marginal efficacy, intra-ventricular corticosteroids are used in some cases (not repeated). Some are actively recommended against due to efficacy.
Biological targeted therapies
No strong random clinical trial evidence suggesting a beneficial effect over placebo despite preclinical evidence for involvement of pathways in OA. More studies needed.
surgical therapies
Only joint alignment surgery esp. high tibial osteotomy and arthroplasty have evidence for efficacy, Anterior cruciate ligament repair while increase joint stability do not alter long-term OA risk supporting that factors beyond mechanics along play a role in post-traumatic OA pathophysiology.
random ass statistics
50% patients dont have pain and functional status well assessed
2/3 patients not offered non-drug effective treatments
2/3 patients receive inappropriate drug regaments