psoriatic arthritis , anklylosing spondylitis, reactive arthritis & septic arthritis Flashcards
What percentage of people with psoriasis develop Psoriatic Arthritis (PsA)?
Approximately 8% of individuals with psoriasis develop Psoriatic Arthritis (PsA).
At what age does Psoriatic Arthritis commonly begin?
Psoriatic Arthritis commonly begins between the ages of 30 and 50.
What percentage of PsA patients can have the condition without psoriasis?
10-15% of patients can have Psoriatic Arthritis without having psoriasis.
What is dactylitis, and how often does it occur in PsA patients?
Dactylitis is a distinctive sausage-like swelling affecting one or two digits, occurring in around 25% of patients.
Name some features in the history and examination of Psoriatic Arthritis.
- Personal or family history of psoriatic rash on extensor surfaces<br></br>- Joint involvement in hands and feet<br></br>- Dactylitis<br></br>- Eye disease<br></br>- Nail changes (pitting, yellowing, ridges, oncholysis)<br></br>- Enthesopathy (including Achilles tendonitis)
What are the patterns of presentation in Psoriatic Arthritis?
- Symmetrical polyarthritis (20–40%)<br></br>- Asymmetric oligoarthritis (30–55%)<br></br>- Distal interphalangeal joint disease (7–17%)<br></br>- Arthritis mutilans (5%)<br></br>- Spondylitic pattern +/– sacroiliitis (5–30%)
Describe arthritis mutilans and its characteristics.
Arthritis mutilans is an aggressive and destructive form of Psoriatic Arthritis affecting 5% of patients. It involves the reabsorption of bone, collapse of soft tissue, and telescoping of the digits.
What blood markers are raised in Psoriatic Arthritis, and what is the status of rheumatoid factor (RF)?
Raised inflammatory markers are present, but rheumatoid factor (RF) is negative in Psoriatic Arthritis.
What imaging modalities are used for investigating Psoriatic Arthritis?
- X-ray: Detects joint damage, marginal erosions, ‘whiskering’, osteolysis, and enthesitis.<br></br>- MRI: Detects early inflammatory changes.<br></br>- Ultrasound: Detects enthesitis and synovitis.
Name some non-medical management options for Psoriatic Arthritis.
Physiotherapy, occupational therapy, orthotics, and chiropodist are non-medical management options.
List some symptomatic medical treatments for Psoriatic Arthritis.
- Corticosteroids/joint injections<br></br>- Topical steroid eyedrops
What are the three categories of disease-modifying medications used for Psoriatic Arthritis?
- NSAIDs<br></br>2. csDMARDs (e.g., methotrexate, sulfasalazine, leflunomide)<br></br>3. Anti-TNF (bDMARD) in severe cases unresponsive to NSAIDs and methotrexate.
Provide examples of biologics used in the treatment of Psoriatic Arthritis.
- Secukinumab - bDMARD, anti-IL17<br></br>2. Targeted synthetic DMARDs (e.g., tofacitinib - Janus kinase inhibitor) used after the failure of csDMARDs +/– bDMARDs.
What are the first-line disease-modifying medications for Psoriatic Arthritis?
First-line disease-modifying medications include NSAIDs and csDMARDs.
What is Psoriatic Arthritis, and how is it associated with psoriasis?
Psoriatic arthritis is an inflammatory arthritis associated with psoriasis. It ranges in severity from mild joint stiffness to complete joint destruction in arthritis mutilans.
What percentage of patients with psoriasis develop Psoriatic Arthritis, and when does it typically occur?
Psoriatic arthritis occurs in 10-20% of patients with psoriasis, usually within 10 years of developing the skin condition. It can precede skin changes and may occur at any age, most commonly in middle age.
What are the patterns of Psoriatic Arthritis, and which ones are the most common?
There are five recognized patterns: Asymmetrical oligoarthritis, Symmetrical polyarthritis, Distal interphalangeal predominant pattern, Spondylitis, and Arthritis mutilans. The most common patterns are Asymmetrical oligoarthritis and Symmetrical polyarthritis.
Describe the features of Arthritis mutilans, the most severe form of Psoriatic Arthritis.
Arthritis mutilans is the most severe form, affecting the phalanges (bones of fingers and toes). It involves osteolysis (bone destruction) around the joints, leading to progressive shortening of the digits. The telescoping digit appearance results from skin folding as the digit shortens.
How can Psoriatic Arthritis be distinguished from rheumatoid arthritis based on joint involvement?
Psoriatic arthritis tends to affect the distal interphalangeal (DIP) joints and the axial skeleton, distinguishing it from rheumatoid arthritis. Rheumatoid arthritis typically does not affect these joints.
What are some signs of Psoriatic Arthritis observed in the skin and nails?
Signs include psoriasis plaques on the skin, nail pitting, onycholysis (nail separation from the nail bed), dactylitis (inflammation of the entire finger), and enthesitis (inflammation at tendon insertion points into bone).
What is the Psoriasis Epidemiological Screening Tool (PEST), and how is it used in screening for Psoriatic Arthritis?
PEST is a screening tool involving questions about joint pain, swelling, arthritis history, and nail pitting. A high score triggers a referral to a rheumatologist, aiding in the identification of Psoriatic Arthritis in patients with psoriasis.
What are the characteristic x-ray changes seen in Psoriatic Arthritis?
X-ray changes include periostitis (inflammation of the periosteum), ankylosis (fusion of bones at the joint), osteolysis (bone destruction), and the “pencil-in-cup” appearance, associated with arthritis mutilans, featuring erosion and a cup-like appearance in the joint.
What is the classic x-ray finding in the digits associated with arthritis mutilans?
The “pencil-in-cup” appearance is the classic x-ray finding in the digits. It involves erosion of bones at the joint, creating a cup-like appearance on one side and a pointed appearance resembling a pencil on the other side. This appearance is specific to arthritis mutilans.
How is the management of Psoriatic Arthritis coordinated, and which professionals are involved?
The management involves coordination between dermatologists, rheumatologists, and a multidisciplinary team. Treatment may include NSAIDs, steroids, DMARDs (e.g., methotrexate, leflunomide, sulfasalazine), and anti-TNF medications (etanercept, infliximab, adalimumab), as well as Ustekinumab, a monoclonal antibody targeting interleukin 12 and 23.
What is the characteristic feature of ankylosing spondylitis in the axial skeleton?
Ankylosing spondylitis is characterized by partial or complete fusion and rigidity of the spine, leading to a chronic inflammatory disease of the axial skeleton.
What is the genetic predisposition associated with ankylosing spondylitis, and how common is it?
Ankylosing spondylitis has a genetic predisposition, with 90% of cases associated with HLA B27. There is often a strong family history of the condition.
What is the typical age of onset for ankylosing spondylitis?
The typical age of onset for ankylosing spondylitis is 20-40 years.
What are the clinical features related to articular symptoms in ankylosing spondylitis?
Articular symptoms include inflammatory spinal and back pain, with a gradual onset of dull pain that progresses slowly. Early morning stiffness lasting more than 30 minutes that improves with activity is a common feature. Peripheral arthritis, though rare, may also occur in joints like the knee, shoulders, and hips.
What are the signs associated with the lumbar spine in ankylosing spondylitis?
Patients with ankylosing spondylitis often display restricted movements in the lumbar spine. Schobers test is used to measure lumbar spine flexion, involving measurements below and above the posterior superior iliac crests while the patient bends forward. Normal extension should exceed 20cm.
How does ankylosing spondylitis manifest in the thoracic spine?
In the thoracic spine, dorsal kyphosis can develop as the disease progresses. Some cases exhibit reduced chest expansion, defined as less than 5 cm.
What are the manifestations of ankylosing spondylitis in the cervical spine?
Movements at the cervical spine can be globally reduced, with the neck forced into a flexed position by dorsal kyphosis. The occiput-to-wall distance is measured with the patient standing against a wall, providing a readout of fixed neck flexion (normal = 0).
What signs indicate tenderness in ankylosing spondylitis?
Tenderness in ankylosing spondylitis is observed in the sacroiliac joints and may include inflammatory enthesitis, such as the Achilles tendon and iliac crests, which is painful on palpation.
Describe the characteristic posture seen in late ankylosing spondylitis.
Late-stage ankylosing spondylitis is characterized by the loss of lumbar kyphosis with pronounced cervical lordosis, resulting in a ‘question mark’ posture.
How is the Schobers test used to assess ankylosing spondylitis?
The Schobers test is used to measure lumbar spine flexion in ankylosing spondylitis. It involves measuring 5cm below and 10cm above the posterior superior iliac crests while the patient is upright. The patient then bends forward, and the distance is remeasured. In normal situations, the extension should exceed 20cm.
What is the significance of the occiput-to-wall distance in ankylosing spondylitis assessment?
The occiput-to-wall distance is measured to assess ankylosing spondylitis. It provides a readout of fixed neck flexion, with a normal distance being 0.
What is the characteristic appearance on x-rays for ankylosing spondylitis?
X-rays of ankylosing spondylitis reveal characteristic features such as periostitis (inflammation of the periosteum), ankylosis (fusion of bones at the joint), osteolysis (bone destruction), and the “bamboo spine” appearance due to syndesmophyte formation.
How is the management of ankylosing spondylitis coordinated, and what are the potential treatment options?
Management involves coordination between healthcare professionals. Treatment options may include NSAIDs, physiotherapy, and, in severe cases, biologics such as TNF inhibitors. A multidisciplinary approach is essential for optimal care.
What is Ankylosing Spondylitis (AS), and what parts of the body does it primarily affect?
Ankylosing Spondylitis is an inflammatory condition affecting the axial skeleton, mainly the spine and sacroiliac joints, causing progressive stiffness and pain. It is also referred to as axial spondyloarthritis.
What is the strong genetic link associated with Ankylosing Spondylitis, and how common is it?
Ankylosing Spondylitis has a strong link with the HLA-B27 gene, present in around 90% of AS patients. However, it is estimated that less than 10% of people with the gene will develop AS. The condition is more common in men, although women can also be affected.
Describe the typical presentation of Ankylosing Spondylitis in terms of age, gender, and symptoms.
The typical presentation is a young adult male in their 20s, with symptoms developing gradually over at least three months. The main presenting features include pain and stiffness in the lower back and sacroiliac pain in the buttock region.
How do symptoms of Ankylosing Spondylitis vary with rest and activity?
Symptoms of Ankylosing Spondylitis worsen with rest, including increased pain and stiffness. Conversely, symptoms improve with movement and activity. The pain and stiffness are typically worse at night and in the morning, taking at least 30 minutes to improve in the morning.
What additional symptoms and problems can be associated with Ankylosing Spondylitis?
Additional symptoms and problems associated with Ankylosing Spondylitis include chest pain related to costovertebral and sternocostal joints, enthesitis (inflammation where tendons or ligaments insert into bone), dactylitis (inflammation of the entire finger), vertebral fractures, and shortness of breath related to restricted chest wall movement.
What are the key associations with Ankylosing Spondylitis, as remembered by the “5 As” mnemonic?
The key associations with Ankylosing Spondylitis can be remembered using the “5 As” mnemonic: Anterior uveitis, Aortic regurgitation, Atrioventricular block (heart block), Apical lung fibrosis (fibrosis of the upper lobes of the lungs), and Anemia of chronic disease.
What is the purpose of Schober’s Test, and how is it performed?
Schober’s test assesses spinal mobility. The patient stands straight, and the L5 vertebra is located. Points are marked 10cm above and 5cm below this level. The patient bends forward, and the distance between the points is measured. A length of less than 20cm indicates restricted lumbar movement, supporting a diagnosis of ankylosing spondylitis.
What are the key investigations for ankylosing spondylitis, and what information do they provide?
Key investigations include inflammatory markers (CRP and ESR), HLA B27 genetic testing, X-ray of the spine and sacrum, and MRI of the spine showing bone marrow edema early in the disease. Inflammatory markers may rise with disease activity, and X-rays can reveal characteristic features such as a “bamboo spine” and other changes.
What is the typical x-ray finding in the later stages of ankylosing spondylitis?
In the later stages of ankylosing spondylitis, a “bamboo spine” is a typical x-ray finding, indicating fusion of the sacroiliac and spinal joints. X-rays can also show squaring of vertebral bodies, subchondral sclerosis and erosions, syndesmophytes, ossification of ligaments, discs, and joints, as well as fusion of facet, sacroiliac, and costovertebral joints.
How is medical management approached for ankylosing spondylitis, and what are the first-line options?
Medical management involves controlling symptoms and preserving function. First-line options include non-steroidal anti-inflammatory drugs (NSAIDs). Second-line options are anti-TNF medications (e.g., adalimumab, etanercept, or infliximab). Third-line options include secukinumab or ixekizumab (monoclonal antibodies against interleukin-17) and upadacitinib (JAK inhibitor).
What additional management strategies are recommended for ankylosing spondylitis?
Additional management includes physiotherapy, exercise, and mobilization. Avoiding smoking is advised. Bisphosphonates are recommended for osteoporosis. Intra-articular steroid injections may be considered for specific joints. Severe joint deformity may require surgery, and the rheumatology multidisciplinary team is involved in overall patient management.
What is the defining characteristic of Reiter’s syndrome, and what is its triad?
Reiter’s syndrome is an infection-induced systemic illness characterized by an inflammatory synovitis. The triad includes urethritis, conjunctivitis/uveitis/iritis, and arthritis.
What are the most common preceding infections associated with Reiter’s syndrome?
The most common preceding infections are urogenital, such as chlamydia and neisseria, and enterogenic, including salmonella and campylobacter.
What is the age range and sex distribution commonly observed in Reiter’s syndrome?
Reiter’s syndrome commonly presents in early adulthood, between the ages of 20 and 40, with an equal sex distribution.
What is the role of HLA B27 in Reiter’s syndrome?
Reiter’s syndrome is associated with HLA B27 positivity.
How does Reiter’s syndrome manifest in response to an infection?
Reiter’s syndrome occurs in response to an infection in another part of the body. Large joints, such as the knee, become inflamed around 1-3 weeks following the infection, triggering an autoimmune arthropathy.
What are the common symptoms of Reiter’s syndrome, particularly related to arthritis?
Common symptoms include peripheral arthritis, typically asymmetrical oligoarthritis, starting 1-4 weeks after infection. Large joints of the lower limbs are most commonly affected. Axial arthritis, especially of the sacroiliac joints and lumbosacral spine, may occur in up to 40% of patients and is associated with HLA-B27.
What constitutional symptoms may be observed in Reiter’s syndrome, and why is sepsis a concern?
Constitutional symptoms include fever, fatigue, and malaise, which can be severe and mimic sepsis (which needs to be excluded).
What signs are associated with Reiter’s syndrome, apart from arthritis?
Signs include dactylitis, mucocutaneous lesions (keratodermia blenorrhagica, circinate balanitis, painless oral ulcers, hyperkeratotic nails), ocular lesions (conjunctivitis, iritis, anterior uveitis), and visceral manifestations (mild renal disease, carditis).
Describe the triad that defines Reiter’s syndrome.
Reiter’s syndrome is characterized by the triad of urethritis, conjunctivitis/uveitis/iritis, and arthritis.