W32 Osteoarthritis And Rheumatoid Arthritis Flashcards

1
Q

What are the medicines used for Osteoarthritis and Rheumatoid arthritis?

A
  • Paracetamol
    • NSAIDs
    • Ibuprofen, Naproxen, or Diclofenac, or a Coxib (such as Celecoxib or Etoricoxib)
    • Opioids
    • Glucocorticoids
    -Prednisolone, methylprednisolone and triamcinolone
    • Conventional Disease Modifying Anti-Rheumatic Drugs (cDMARDs)
    -Methotrexate, Leflunomide, Sulfasalazine, Hydroxychloroquine
    • Tumor Necrosis Factor Alpha (TNFα) Inhibitors
    • Biological Disease Modifying Anti-Rheumatic Drugs (bDMARDs)
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2
Q

What is Arthritis?

A

● ‘inflammation of joint‘
● In common terms, arthritis is used to describe one of two conditions affecting joints:
o Osteoarthritis
-Common, slowly progressive deterioration in joints
o Rheumatoid arthritis
-An autoimmune disease of the joints

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3
Q

What is osteoarthritis?

A

• OA is the most common cause of arthritis, the most common disease of synovial joints, and is a major cause of disability.
• Age-related, progressive disorder
• Commonly affects weight bearing joints
• Knees, hips, spine, (hands)
• Characterized by:
• Progressive deterioration and loss of articular cartilage
• Pain and limitation of motion
• Progressive disability
• Inflammation may or may not be present
• Joint pain often eased by rest
• Pain worsens at end of the day

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4
Q

Diagnostics of Osteoarthritis:

A
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5
Q

What are the OA risk factors? (6)

A
  • Age
  • Obesity
  • Injury
  • Occupational overuse
  • Female gender
  • Family history
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6
Q

Which joints are affected in OA?

A

Any joint can be affected by OA
Joints most affected:
- Neck, lower back, hips, base of thumb, ends of fingers, knees, base of big toe

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7
Q

What are the treatment goals in osteoarthritis? (4)

A
  • relieve pain;
  • maintain mobility and function;
  • prevent further joint damage;
  • improve the patient’s mental health and quality of life
    =Minimise impact on ADL & QoL
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8
Q

What is the management of Osteoarthritis?

A
  • Patient education and counselling
  • Physical therapies
  • Physiotherapy and occupational therapy
  • Correction of exacerbating factors
  • Pharmacotherapy
  • Simple analgesic (Paracetamol, Aspirin)
  • NSAIDs (Topical vs systemic)
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9
Q

Non-pharmacologic approaches in OA?

A
  • Weight loss - critical
  • Physiotherapy, exercise programs,
    -Strengthen supporting muscles
  • Massage, hot or cold packs (?acupuncture)
  • Devices and aids (e.g., walking sticks)
  • Surgery (e.g., joint debridement or joint replacement,)
    -30% of patients
  • Not effective: Magnets & copper bracelets
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10
Q

Pharmacologic management – General principles in OA? (goals)

A
  • Relieve symptoms (pain and stiffness)
  • Improve joint function
  • OA mainly affects older people
    -co-existing conditions
    -use conservative approach
  • Individualise therapy based on stage and severity of disability
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11
Q

Medication options for OA?

A
  • Paracetamol
  • Topical preparations
  • Opioids
  • NSAIDs
  • Intra-articular corticosteroids
  • Intra-articular hylans
    -For knee (not usually recommended)
  • Anti-depressant
  • Glucosamine & Chondroitin
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12
Q

Summary of OA management

A

Simple analgesics
* (e.g., Paracetamol)
Topical or oral NSAIDs PRN
* Consider topical capsaicin
Higher dose NSAIDs (plus Paracetamol) or Opioids (plus Paracetamol)
Corticosteroids (in severely affected joint that is inflamed)
* Intra-articular corticosteroid injection
Antidepressants (to alleviate depression associated with chronic pain and improve analgesic response)

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13
Q

Rheumatoid Arthritis (RA)
A joint affected by rheumatoid arthritis has what features? (3)
Osteoarthritis? (2)

A
  1. Inflamed synovium spreading across joint surface
  2. Thinning of cartilage
  3. Erosion into corner of bone
  4. Thinned cartilage
  5. Bone ends rub together
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14
Q

Short description of RA?

A
  • RA – a chronic, progressive, inflammatory, systemic disease that primarily affects synovial joints.
  • In the UK, about 1% of the population is affected.
  • RA is 2–4 times **more common in women than in men
  • Approximately one–third of people stop work because of RA within 2 years of its onset and this increases thereafter.
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15
Q

Immunopathology of RA?

A

➢Inflammation is the hallmark of active RA
➢ Activation of T cells by macrophages and unidentified antigens cause cytokine
release.
➢ Cytokines are also produced by synovial fibroblasts.
➢Primary problem is inflammation of the synovium – if uncontrolled –> bone erosions and structural damage to the joints
➢TNFa and IL-1, IL-2, IL-4 and IL-8 are important in the initiation and maintenance of inflammation and cartilage and bone damage and synovitis.

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16
Q

Clinical presentation of RA?– usually symmetrical

A

*Stiffness
*Usually, ~1 hour in the morning
*Swelling
*Tissue around joint may feel soft and spongy
*Red and warm
*Loss of function
*(e.g., grip strength)
*Systemic manifestations
*Eyes, lungs, heart, nerves….
*Often initial presentation is nonspecific inflammation
*Fever, malaise, weakness etc.

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17
Q

What is the Classic criteria for RA?

A

A diagnosis of definite RA requires at least four of the following criteria:
1. Morning stiffness for ≥ 1 h.
2. Arthritis of three or more joints and soft tissue swelling.
3. Arthritis of hand joints (wrist, MCP or PIP joints).
4. Symmetrical arthritis.
5. Rheumatoid nodules.
6. Serum RF (positive in ˂ 5% of normal control subjects).
7. Radiographic changes. Hand X-ray changes typical of RA must include erosions or unequivocal bony decalcification.

(1-4 must be continuously present for at least 6 weeks)

18
Q

Investigations – common investigations in patients with RA (Primary Care)? (4)

A
  • Offer – a blood test for rheumatoid factor (RF) in adults with RA who are found to have synovitis on clinical examination (positive in 60-70% of people with RA).
  • Consider – anti-CCP antibodies in adults with suspected RA if they are negative for RF
    (positive in about 80% of people with RA).
  • Arrange – X-ray the hands and feet in adults with suspected RA and persistent synovitis.
  • Consider – FBC, RFT, LFT, CRP & ESR
19
Q

Conclusive diagnosis of RA?(4)

A
  • The occurrence of early morning stiffness
  • Symmetrical painful polyarthritis
  • High RF titre
  • Joint erosions

ACR criteria 1, 2, 4, 6 and 7

20
Q

Functional assessment of RA: (monitor response to treatment

A
  • Duration of morning stiffness
  • Grip strength
  • Functional questionnaire: e.g. ability to dress, walk, open doors, turn taps, pick up small objects
  • Degree of joint movement: e.g. fingers, arms, hips, knees; chest expansion, spinal extension when stooping
  • Ability to perform activities of daily living: e.g. work related tasks, maintaining the home, child care
21
Q

The aims of the RA management are..?

A
  • Relieve pain and discomfort and ameliorate symptoms
  • Arrest or limit disease progression and, if possible, reverse pathological changes
  • Maintain mobility and function and promote the best possible quality of life.
22
Q

Management of RA?– In simple words

A
  • Non-pharmacological therapies
  • Pharmacological therapies
  • Drugs to control the disease process
  • Drugs for symptoms
23
Q

Management of RA?

A
  • Patient education and counselling
  • Physical: physiotherapy, osteopathy, occupational therapy, appliances, etc.
  • Social: domestic assistance, modification of the home environment, financial support
  • Pharmacotherapy: analgesics, anti-inflammatory agents (i.e., NSAIDs, anti-
    cytokine drugs and corticosteroids), slow-acting (‘disease-modifying’) antirheumatic drugs (i.e., immunoregulators and antiproliferative
    immunosuppressants)
  • Appropriate management of anaemia and other complications
  • Psychiatric support
  • Surgery: synovectomy, arthroplasty and other joint surgery
24
Q

Non-pharmacologic management of RA?

A
  • Patient education
  • Physiotherapy
  • Occupational therapy
  • Hand exercise programme
  • Podiatry
  • Psychological interventions
  • Diet and complementary therapies
    -Mediterranean diet
  • Smoking cessation
    -Linked to poor progression
  • Cardiovascular risk modification
    -The systemic inflammation increases cardiac risk and patients should be monitored
25
Q

Pharmacological therapies for RA?

A
  • Drugs to control the disease process
    -DMARDs & bDMARDs
    Drugs for symptoms
  • Corticosteroids (prednisolone)
  • NSAIDs
  • Paracetamol
  • Fish Oil
26
Q

Management of suspected RA:
What symptoms would lead to a referral? (3)
What to consider prescribing?

A
  • Refer urgently, within 3 working days of presentation – even with a normal acute phase (i.e., negative anti-CCP antibodies or RF) if a patient has the following:
  1. Small joints of the hands or feet are affected.
  2. More than one joint is affected.
  3. There has been a delay of 3 months or longer between the onset of symptoms and the person seeking medical advice.
  • Consider – NSAIDs at the lowest effective dose for the shortest duration possible (until rheumatology appointment)
  • Ibuprofen, naproxen, diclofenac, or a coxib (e.g., celecoxib or etoricoxib)
  • Consider potential GI, liver and cardio-renal toxicity, and the person’s risk factors, including age and pregnancy.
  • Offer – proton pump inhibitor (PPI) with NSAIDs.
  • Do not prescribe a glucocorticoid in primary care before a specialist assessment is carried out.
27
Q

Methotrexate POM
dose?
freq?
dosage form?

A
  • First line therapy for RA
  • MTX is immunosuppressant, folate anatagonist
  • Dose: 7.5 - 25mg ONCE weekly
  • MHRA Warning this is a ONCE WEEKLY dose.
  • Fatalities have been reported due to prescribing and dispensing errors
  • Dosage form: tablets, a liquid, and pre-filled injection pens or syringes
  • Patient card – to record the details of patients’ weekly dose and the day they take it.
  • Refer to local guideline - Shared care protocol, Shared care prescribing and monitoring guidance
27
Q

Folic acid:

A
  • 5mg once weekly, preferably the day after the methotrexate – should not be given on the same day as methotrexate.
  • Folic acid reduces toxic effects and improves continuation and compliance – can be
    given more frequently (up to 5mg daily EXCEPT for day that methotrexate is taken)

PA: Do not take folic acid on the same day as your methotrexate. It can stop your medicine from working properly.

28
Q

Monitoring:

A

Baseline
* FBC, creatinine & electrolytes, LFTs, and CXR (unless CXR done within the last 6 months).
* Lung function tests should be undertaken in patients with pre-existing lung disease
or respiratory symptoms before starting treatment.

During treatment
* FBC, LFTs and creatinine & electrolytes every 1- 2 weeks for first four to six weeks then monthly – This time period may vary depending on how quickly patient is titrated up to maintenance dose
* NB: FBC and LFTs are required two weeks after any dose increase

29
Q

Adverse effects of MTX? (for info- there are loads)

A

Myelosuppression- sore throat, fever malaise, bleeding, brusing, purport
Pulmonary- cough, dyspnoea, fever
Hepatic- Abnormalities of liver function
Gastrointestinal- Nausea, vomiting, anorexia, diarrhoea
Skin- rash, alopecia, skin ulceration
Renal- nephrotoxicity and renal failure
Reproductive- reduced oogenesis and spermatogenesis during treatment, Teratogenic

30
Q

Special recommendations for MTX?

A
  • Live vaccines should generally be avoided in patients taking methotrexate.*
  • Patients receiving methotrexate should be advised to limit their alcohol intake well within national recommendations.
  • All patients, male and female, should be advised against conception and pregnancy during treatment with MTX as it is an abortifacient as well as a teratogenic drug. Patients should be advised to continue contraception for at least 6 months after stopping MTX.
  • Methotrexate must be avoided in breast-feeding as the drug may be secreted into the breast milk.

*Reccomended to take pneumococcal and flu vaccines as MTX is an immunosuppressant

31
Q

Leflunomide
when to use?
common adverse effects?

A
  • Leflunomide may be used as monotherapy in patients who have intolerance or contraindications to use of MTX in RA, or it may be used in combination with methotrexate for patients with suboptimal response to MTX alone.
    Leflunomide is used for moderate to severe RA.
  • Common adverse effects include headache, diarrhoea, and nausea. Other effects are weight loss, allergic reactions, including a flu-like syndrome, skin rash, alopecia, and hypokalemia.
32
Q

When to avoid leflunomide? (2)
Monitoring?

A
  • The drug is not recommended in patients with liver disease as it can be
    hepatotoxic.
  • Leflunomide is contraindicated in pregnancy

Monitoring parameters include signs of infection, complete blood count,
electrolytes, and liver enzymes.
-Frequency: at baseline and every 2 weeks for the first 6 months then every 8 weeks

33
Q

Sulfasalazine (SSZ)
When to give to pt?
Common adverse effects?
Monitoring?

A

Sulfasalazine (SSZ)* Sulfasalazine – similar to leflunomide in the treatment of RA.
* The onset of activity is 1 to 3 months (faster onset of action & less toxic)
* Common adverse effects are (nausea, vomiting, anorexia) and leukopenia.
* Close monitoring of full blood counts (including differential white cell count and platelet count) is necessary initially, and at monthly intervals during the first 3 months

34
Q

Hydroxychloroquine:
When to use?
Safe?
Use in pregnancy?
Adverse effects?

A
  • Hydroxychloroquine is used for early, mild RA, and may be combined with MTX.
    -Onset of effects takes 6 weeks to 6 months.
  • Hydroxychloroquine has less adverse effects on the liver and immune system than other DMARDs.
  • Hydroxychloroquine can be used with caution in pregnancy.
  • Hydroxychloroquine may cause ocular toxicity, including irreversible retinal damage and corneal deposits, CNS disturbances, GI upset, and skin discoloration and eruptions.
35
Q

Further Pharmacological Management: (RA)

A
  • Tumor necrosis factor (TNF) alpha inhibitor: (specialist)
    -adalimumab, certolizumab pegol, etanercept, golimumab, or infliximab (initiated by specialist)
  • Biological DMARDs (Under expert supervision)
    -abatacept, sarilumab, or tocilizumab
  • Targeted synthetic DMARDs
    -baricitinib, filgotinib, tofacitinib, or upadacitinib
  • If adequate control is not achieved – Orthopaedic surgery
36
Q

Supplements for RA and OA? (4)

A
  • Glucosamine sulphate 750 – 1500 mg
    BD for 3 – 6 months –> OA
  • Capsaicin cream –> OA
  • Selenium? –> RA
  • Fish oil? –> RA
37
Q

Summary of RA:

A
  • Most people with RA produce antibodies (‘rheumatoid factors’)
    -Seropositive people usually have more aggressive course than seronegative people
  • DMARDs (and bDMARDs) can be used to induce an inflammatory remission
    -therefore, significantly prevent joint damage
  • All patients with RA should commence a DMARD as soon as possible
  • DMARDs are generally associated with significant toxicity, though, and require careful monitoring and patient counselling
  • The choice of initial DMARD depends upon patient factors and disease severity
    -MTX is the gold standard if no contra-indication
  • Some patients commence on >1 DMARD initially
38
Q

Generalised Clinical Differences OA vs RA

A

Osteoarthritis (OA)
* Disease caused by cartilage destruction
* Affects bigger joints
* Asymmetrical
* May not be inflammatory
* Worse at end of day, after exercise
* Rheumatoid factor negative

Rheumatoid Arthritis (RA)
* Disease with strong immune component
* Affects any joints
* Symmetrical
* An inflammatory disease
* Worse at start of day, exercise can help
* Rheumatoid factor positive

39
Q

Clinical feature of OA vs RA:

A

OA:
- can affect different joints
- tends to be one sided
- typically occurs later in life but can start earlier in joints already affected by RA
- stiff less than 30 mins in morning
- joints feel bony but no soft swelling

RA:
often starts in small joints
- pain is in symmetric joints
- morning pain and stiffness for more than 30 mins