Musculoskeletal/Orthopaedic/Rheumatology Flashcards
A 28-year-old man is brought to the Emergency Department after he had an accident while driving a motorcycle and had his right ankle injured. On examination, his vital signs are stable. The right ankle joint is laterally displaced and there is a laceration over the joint. Which one of the following is the most important initial step in management?
A. Wound debridment.
B. Tetanus immunization.
C. Intravenous antibiotics.
D. Reduction of the displacement.
E. X-ray of the joint.
D. Reduction of the displacement
Open fractures and/or dislocations are defined as the bone and/or joint being exposed to the external environment, or when the fracture or dislocation is caused by blunt or penetrating forces sufficient to disrupt or penetrate skin, subcutaneous tissue, muscle fascia, muscle, and/ or the bone or joint. Open fractures are often contaminated by foreign material (e.g., clothing, grass, dirt, gravel), dead or devitalized tissue, and bacteria.
`Always follow the following rules in open fractures/ dislocations:
- Remove any gross contamination off the wound. No provisional irrigation or debridement is performed at this stage.
- Take photographs of the wound and dress it with wet sterile cover (the photographs are taken, so that other treating physicians do not need to uncover the wound to see it)
- Give patient analgesic (preferably intravenously to both control the pain and prepare for a reduction in the emergency department). Morphine is a good option.
- By gentle traction, reduce the fracture and correct misalignments as much as possible.
- Start the patient on intravenous prophylactic antibiotics.
- Give the patient tetanus prophylaxis if indicated.
- Obtain X-rays.
- Urgently arrange for transferring the patient to the operating room for surgical wound debridement and definite treatment of the fracture and dislocation.`
In this scenario the most appropriate initial management would be reduction of the dislocation by gentle traction after non-surgical removal of any gross contamination, and analgesia. The patient then should be started on intravenous antibiotics and receive tetanus prophylaxis.
X-ray of the joint (option E) is required pre-operatively to visualize the anatomical disruption. Wound debridement (option A) is crucial but should be performed in the operating room ideally with 1-2 hours of presentation.
A 72-year-old man was brought to the emergency department after he sustained a fracture of his left hip following a fall at home. Initial pain management was considered and the
operation carried out with intramedullary nail placement. Today, he is being discharged. Which one of the following is the most important management option to consider for him on
discharge?
A. Painkillers.
B. Walker.
C. Crutches.
D. Low molecular weight heparin.
E. Warfarin
A Painkillers.
According to guidelines provided by the Agency for Clinical Innovation (ACI), it is crucial to mobilize patients with hip fracture within 24 hours of the surgery. Pain following hip fracture should be presumed severe and continuous. Effective pain management is a primary goal for patients with a hip fracture, because immobility caused by pain has been associated with the increased risk of the following:
* Pressure ulcers
* Pneumonia
* Venous thromboembolism (VTE)
With greater pain, the likelihood of the following will increase:
* Delirium
* Sleep disturbances
* Depression
Pain control is of significant importance for early mobilization of patients who have undergone hip surgery, because the pain brought on by physical activity is the most important factor preventing from being mobile; therefore, pain control with painkillers play a crucial role in early mobilization.
Pain is often undertreated or poorly controlled in orthogeriatric patients due to:
1. Reluctance or inability of an older patient to request analgesia
2. Reluctance of medical staff to prescribe analgesia in older frail patients
3. Cognitive impairment in patients, making assessment of pain level difficult
Pain management techniques for patients with hip fracture include pharmacological approaches such as paracetamol and opioids and use of femoral nerve block.
(Options B and C) Walking aids such as crutches or walkers should be advised to provide more convenient mobilization, but they are not superior to analgesics, because with pain the patient is unlikely to become physically active and changes posture (e.g. from sitting to standing or walking).
(Option D) LMWH is also important in prevention of VTE in this patient, but this has already been started immediately after the surgery and continued during the hospital stay.
(Option E) Warfarin is not routinely used for prophylaxis of VTE in patients with hip surgery.
A 35-year-old woman is brought to the Emergency Department after she sustained a motor vehicle accident as a frontseat passenger, and had her left ankle injured. On examination, her vital signs are stable. The left ankle joint is laterally displaced and there is a 13-cm laceration over the joint. The left dorsal pedis pulse is barely felt and the foot is cold and pale. The condition is diagnosed as open fracture/dislocation of the ankle joint. Which one of the following is the most important step in preventing wound infection and ensuing complications?
A. Intravenous antibiotics.
B. Wound debridment.
C. Tetanus prophylaxis.
D. Reduction of the displacement.
E. X-ray of the joint.
B. Wound debridment.
This patient has an open fracture/dislocation of the ankle joint with vascular compromise. Open fractures/dislocations are characterized by the bone and/ or joint exposure to external environment, or when the fracture or dislocation is caused by blunt or penetrating forces sufficient to disrupt or penetrate the skin, subcutaneous tissue, muscle fascia, muscle, and/ or the bone or joint. Open fractures are often contaminated by foreign material (e.g., clothing, grass, dirt, gravel), dead or devitalized tissue and bacteria.
Always follow the following rules in open fractures / dislocations:
1. Remove any gross contamination off the wound. No provisional irrigation or debridement is performed at this stage.
2. Take photographs of the wound and dress it with wet sterile cover (the photographs are taken, so that other treating physicians do not need to uncover the wound to see it.)
3. Give patient analgesic (preferably intravenously to both control the pain and prepare for a reduction in the emergency department). Morphine is a good option.
4. By gentle traction, reduce the fracture and correct misalignments as much as possible.
5. Start the patient on intravenous prophylactic antibiotics.
6. Give the patient tetanus prophylaxis if indicated.
7. Obtain X-rays.
8. Urgently arrange for transferring the patient to the operating room for surgical wound debridement and definite treatment of the fracture and dislocation.
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The question, however, asks about the most important step in preventing infections and consequent complications
. Debridement of all devitalized soft tissues and bone all the way down to the bone is the most crucial step in preventing the infection and the consequent adverse outcomes such as delayed healing, amputation, etc.
Option A: Prophylactic antibiotics are started prior to debridement and definite treatment, and are of great importance; however, debridement remains the cardinal step in preventing infections.
Option C: Tetanus prophylaxis should be given to the patient if indicated but this does not prevent other infections if adequate debridement is not carried performed.
Wound debridement is always crucial but should be performed in the operating room after the above measures have been undertaken; therefore, it is not a priority but an extremely
important step in preventing infections.
A 57-year-old construction worker man presents to your practice with the hand deformity illustrated in the accompanying photograph. He works with a drilling machine and has tingling sensation in his hand after work. He drinks 2 bottles of beers every day and even more on weekends. Which one of the following could be the most likey cause of his problem?
A. Alcohol consumption.
B. An autoimmune process.
C. Vibration injury.
D. Direct trauma.
E. Injury to the ulnar nerve.
A. Alcohol consumption.
The picture shows puckering of palmar skin and a nodule at the base of fourth (ring) finger which are highly suggestive of Dupuytren’s contracture (DC). DC is caused by fibrous hyperplasia of palmar fascia leading to nodular formation and contracture over the fourth and fifth fingers commonly.
This condition occurs in 10% of males over the age of 65 years particularly in those of North European descent. There is a genetic predisposition for the disease and the condition is assumed to have an autosomal dominant inheritance, but for clinical presentation to develop other factors are hypothesized to be involved.
An association between DC and some conditions have been well-established. These conditions are as follows:
-Male gender
-Alcohol Excess
-Smoking
-Liver cirrhosis
-COPD
-Diabetes mellitus
-Heavy manual labour
Of the above factors, the most common risk factors in descending order are:
-Age
-Alcohol excess
-Sex (male)
-Previous hand injuries
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In this man’s case, excess alcohol drinking can be the most likely contributing factor to his condition. Each bottle of beer contains 1.5 - 2 units of alcohol depending on the size and the alcohol concentration.
The pathophysiology of DC is not well-understood. Proliferation of fibrocytes and inflammatory processes are speculated to be the most likely pathophysiology. The disease is not autoimmune. No nerve is involved in DC.
While playing basketball, a 23-old-man landed on his left foot awkwardly and injured his ankle. He is in the emergency department now. On examination, lateral dislocation of the ankle is evident. Dorsal pedis pulse is absent and the foot looks pale and is cold to touch. Which one of the following would be the next best step in management?
A. Reduce the dislocation in the emergency department.
B. Send the patient to the operating room for reduction under general anesthesia.
C. Immobilize the joint with plaster.
D. Send the patient to the operating room for open reduction and internal fixation.
E. Angiography.
A. Reduce the dislocation in the emergency department.
Early reduction/alignment of a dislocation/fracture is always the most important step in management. This is even more crucial when a dislocation or fracture has caused neurovascular compromise.
In the field (prehospital), if there is evidence of neurovascular compromise such as a cold, discolored, and pulseless or insensate foot, reduction of the dislocation or alignment of the fracture should be tried after the patient is given analgesia with intravenous opiates (morphine). If morphine is not available, intravenous benzodiazepines can be used instead. Reduction and alignment is achieved by gentle in-line traction. Alignment should be maintained en route to the hospital.
In the emergency department, if the reduction/alignment has not been performed in the field, reduction should be attempted as soon as possible even before radiological examination if there is vascular compromise.
By definition, dislocation of the ankle is always considered unstable due to accompanying disruption of the lateral or medial ligaments or the tibiofibular syndesmosis. Ankle dislocation requires immediate orthopedic or podiatric consultation for surgical intervention such as internal or external fixation of any accompanying fracture and repair of capsular or ligamentous tears.
None of the other options take precedence over early reduction of the joint.
Which one of the following is a recognized feature of polymyalgia rheumatica?
A. Weakness of the distal muscle groups.
B. Elevated serum creatine phosphokinase (CPK).
C. An association with bronchial carcinoma.
D. Weight loss.
E. A peak incidence in the fourth decade of life.
D. Weight loss.
Polymyalgia rheumatica (PMR)
is a relatively common inflammatory disease in elderly people (almost never seen before < 50) and a common indication for long-term steroid use. The incidence increases with advancing age. It is more common in women.
PMR has many nonspecific features and a wide range of differential diagnoses. No gold standard diagnostic test is available and the diagnosis is mainly made clinically. About 15- 20% of patients with PMR develop giant cell arteritis (GCA) and 40-50% of those with GCA are found to have associated PMR. Despite the similarities in the age of onset and some clinical manifestations, the relationship between PMR and GCA is not yet clearly established; however, these two disorders are thought to represent different manifestations of a shared disease process.
The symptoms of polymyalgia rheumatica (PMR) include pain and stiffness of the shoulder and hip girdle. The neck may be involved in some patients. The stiffness can be so severe that the patient may have great difficulty getting off the chair, turning over in bed, or raising the arms above shoulder height. Stiffness after periods of rest (gel phenomenon) as well as morning stiffness of more than 30 minutes typically occurs.
Muscle weakness is not a feature of PMR. However, this can be difficult to assess in the setting of pain, especially if symptoms are protracted and untreated, resulting in disuseatrophy. Some patients report the following systemic features:
-Low-grade fever (high, spiking fevers are rare and should prompt evaluation for underlying infection, malignancy, or vasculitis)
- Weight loss
- Malaise and/or fatigue
- Depression
- Anorexia
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Of the options, weight loss can be a manifestation of PMR; however, not all patients with PMR have weight loss or other systemic symptoms.
(Option A) Weakness of distal muscle groups is not a feature of PMR.
(Option B) Creatine phosphokinase elevation is associated with inflammatory processes of muscles or muscle breakdown, none of which occurs in PMR.
(Option C) There is no association between PMR and lung cancer including small cell carcinoma of the lung.
(Option E) PMR/GCA is almost never seen before the age of 50. The average age of onset is 70 years.
TOPIC REVIEW
Several diagnostic criteria for PMR exist. One set of diagnostic criteria is as follows:
-Age of onset 50 years or older
-Erythrocyte sedimentation rate ≥40 mm/h
-Pain persisting for ≥1 month and involving 2 of the following areas: neck, shoulders, and pelvic girdle
-Absence of other diseases capable of causing the same musculoskeletal symptoms
-Morning stiffness lasting ≥30 minutes
-Rapid response to prednisone (≤20 mg)
Michael is a 66-year-old patient of yours, who has osteoarthritis of the left knee. Six months ago and after non-pharmacological measures and paracetamol on an as-needed basis failed to relieve the pain, you started him on regular full-dose paracetamol. Today he is at your practice with the complaint that he is still suffering from severe knee pain despite
taking paracetamol. He is diabetic and has ischemic heart disease and peptic ulcer disease. Which one of the following is the most appropriate option to add to paracetamol at this stage?
A. Celecoxib.
B. Tramadol.
C. Codeine.
D. Slow-release morphine preparations.
E. Diclofenac.
C. Codeine.
For mild to moderate osteoarthritic pain without evidence of inflammation, pharmacological treatment starts with paracetamol. Regular full-dose of paracetamol (up to 4gr/day) even in the absence of pain is superior to taking the medication on an as-needed basis.
If the clinical response to paracetamol is not satisfactory, or if the clinical presentation of osteoarthritis is inflammatory, NSAIDs should be considered with the lowest effective dose or intermittent dosing if symptoms are intermittent. NSAIDs are associated with an increased risk of gastrointestinal problems such as dyspepsia and peptic ulcer disease and are contraindicated in patients with active peptic ulcer disease. Selective COX-2 inhibitors are preferred in these patients. The addition of prophylactic proton pump inhibitors or misoprostol is an alternative.
On the other hand, selective COX-2 inhibitors are associated with an increased risk of cerebrovascular or cardiovascular diseases and should be avoided in patients with a history of these conditions.
This patient has peptic ulcer disease and cardiovascular disease; therefore, NSAIDs and COX-2 inhibitors are inappropriate options for him.
Opiates and tramadol are drugs of choice for the treatment of patients with moderate to severe osteoarthritis, for whom NSAIDs are contraindicated or ineffective in controlling pain.
In this patient with a contraindication to both non-selective NSAIDs (e.g. ibuprofen, diclofenac, naproxen) and celecoxib, the addition of a weak opiate such as codeine will be the next best step in management.
(Option A) Celecoxib is not an appropriate option for this man because he has cardiovascular disease.
(Option B) Although tramadol is effective in the management of OA pain, either as a single therapy or added to paracetamol is associated with more adverse effects and is not considered an option at this stage. Studies showed that tramadol has more adverse effects than diclofenac.
(Option D) Strong opiates (e.g. oxycodone, morphine) are associated with more adverse effects, but about the same efficacy as weak opiates for the management of OA.
(Option E) With peptic ulcer disease, diclofenac is not an appropriate option to consider for this man.
TOPIC REVIEW
Pharmacological management of osteoarthritis of the knee
- Paracetamol – paracetamol (or other simple analgesics) are first-line pharmacological therapy for pain control. Paracetamol is safe and can be used up to 1mg every 4 hours. Patients should be advised to use paracetamol on a regular basis (even in pain-free periods) rather than as-needed because the latter often fails to adequately control the pain.
-Non-steroidal anti-inflammatory drugs (NSAIDs) – addition of NSAIDs is the next best step in management if:
1.Optimal therapy with paracetamol fails to control the pain
2.There is evidence of inflammation, such as pain that is worse with rest, nocturnal pain, and gelling of the joint (stiffness with rest).
3.COX-2 inhibitors have all the adverse effects of NSAIDs, although they seem to be less irritating to the stomach lining; therefore, better choices if there is a risk of GI bleeding
Opiate analgesics and tramadol
Opiate analgesics are used if:
-NSAIDs are contraindicated
-NSAIDs fail to control the symptoms
Opiates have a modest effect in managing moderate to severe OA pain in patients for whom paracetamol is ineffective, and who do not respond to, or have contraindications for NSAIDs. However, most of the research on opioid use has been in short-term trials and long-term efficacy has not been shown.
Intra-articular treatments
-Corticosteroids – a single injection can provide rapid relief for up to 4 weeks. The patient should be advised to rest 24 hours after the injection. This therapy can be used if the patient has an important occasion to participate in or wants to travel. Repeated injections are not as effective.
-Hyaluronan – hyaluronan is given weekly for 3 to 5 weeks. Effect sizes are small. They provide slower onset but longer-lasting (up to 12 weeks) pain relief than corticosteroids.
There is conflicting evidence of the benefit of glucosamine in the treatment of the symptoms of knee OA. There is insufficient evidence to support the benefit of preventing the progression of cartilage loss.
PRACTICE POINTS
-Regular use of full-dose paracetamol (500-1000 mg/4-6 hours, up to 4 mg /day) even when there is no pain, is superior to its use on an as-needed basis.
-Whenever NSAIDs are considered, they should be given with the minimum effective dose for 2-4 weeks and close monitoring of blood pressure, renal function, and gastrointestinal symptoms.
-NSAIDs are contraindicated in patients with active peptic ulcer disease. In those at risk of or with a history of peptic ulcer disease, either the selective COX-2 inhibitor – celecoxib should be used or non-selective NSAIDs be given with prophylactic PPIs.
-Celecoxib must be avoided in patients with a history of cardiovascular diseases such as ischemic heart disease, cerebrovascular disease, etc
A 67-year-old woman presents to your clinic with complaints of painful hips and shoulders and headache. She relates that muscle pain is felt in both arms and hips. She feels her shoulders are stiff and her hips cannot move when she wakes up. It almost takes 40 minutes of painful physical activity for the stiffness to relent. Her appetite is decreased and she
has lost 5 kg. “To make me even more miserable, the terrible headaches have just been started”, she mentions. The headache is felt on the right side and is throbbing with no response to analgesics. On physical examination, she is noted to have bilateral painful restricted movements of shoulder and hip joints. Her right temple is tender to touch. She is
not febrile and the rest of the exam is inconclusive. Which one of the following would be the most appropriate next step in management?
A. Check serum creatine kinase (CK) level.
B. Check the rheumatoid factor.
C. Check ESR.
D. Perform a muscle biopsy.
E. Star the patient on prednisolone.
C. Check ESR.
The clinical picture is highly suggestive of two closely-associated clinical syndromes, polymyalgia rheumatica and giant cell (temporal) arteritis (GCA). The etiology of these two syndromes is unknown. Either of these syndromes can develop solitarily, although in 15-20% of cases both are present. If so, polymyalgia rheumatica invariably precedes temporal arteritis.
The patients are usually older (the 60s or 70s). These conditions are very rare among those younger than 50 years. Women are more commonly affected.
Polymyalgia rheumatica presents with pain and stiffness of the shoulders and hips symmetrically. The cervical spine may be involved. There is marked stiffness usually early in the morning lasting over 30 minutes. The symptoms tend to subside or at least relieve by the end of the day. Constitutional symptoms such as malaise, low-grade fever, anorexia, and
weight loss may be present.
Giant cell arteritis presents with headaches often unresponsive or poorly responsive to analgesics, scalp tenderness, jaw claudication, and weak or absent pulsation of the temporal artery. Not all patients with CGA present with headaches.
When these two conditions are suspected, the next best step in management would be measuring the erythrocyte sedimentation rate (ESR). With an elevated ESR (>40), it is prudent that corticosteroids be started immediately to prevent permanent visual loss.
With visual problems at presentation, intravenous corticosteroids (methylprednisolone) replace the oral route for the first 3 days of therapy.
(Options A and D) Creatine kinase levels or muscle biopsy would come first if myositis was suspected.
(Option B) Serologic tests, such as rheumatoid factor (RF), antinuclear antibodies (ANA), and cyclic citrullinated peptide (CCP) antibodies are typically negative.
(Option E) Corticosteroids (e.g. prednisolone) are indicated if ESR is >40mm/h.
Which one of the following cannot be associated with HLA- B27?
A. Acute anterior uveitis.
B. Ankylosing spondylitis.
C. Reactive arthritis.
D. Behçet disease.
E. Psoriatic arthritis.
D. Behçet disease.
HLA-B27 is found in almost 90% of patients with seronegative spondyloarthropathies.
Seronegative spondyloarthropathies include:
-Ankylosing spondylitis (AS)
-Reactive arthritis
-Psoriatic arthritis
-Inflammatory bowel disease
Anterior uveitis is another possible finding in seronegative spondyloarthropathies; hence, from another standpoint, it could be said that those with anterior uveitis may suffer from a seronegative spondyloarthropathy and consequently be HLA-B27 positive.
Behçet disease is a diffuse vasculitis of unknown origin. The disease is characterized by a triple-symptom complex of:
1. Recurrent oral aphthous ulcers
2. Recurrent genital ulcers
3. Uveitis
Behçet disease has no association with HLA-B27
A 67-year-old man presents to your office with complaints of reduced dexterity of his left hand and difficulty grasping objects. His hand is shown in the following photograph. Which one of the following investigations will confirm the diagnosis?
A. X-ray of the hand.
B. MRI.
C. Ultrasonography of the hand.
D. CT scan of the hand.
E. Blood sugar level.
C. Ultrasonography of the hand.
The picture shows palmar skin puckering and a nodule at the base of the fourth finger, indicative of Dupuytren contracture. The diagnosis is almost always made clinically and no imaging is needed. However, ultrasonography can demonstrate thickening of the palmar fascia and the presence of a nodule. At cases, ultrasonography of the hand is considered if the patient is planned for injection of corticosteroids directly into the cord and avoiding injecting into the flexor tendon.
Since there is an association between Dupuytren contracture and diabetes mellitus, blood sugar level can be measured if the physician is suspicious of diabetes based on history and/or clinical findings. X-ray, CT scan or MRI is almost never indicated.
Treatment options for Dupuytren contracture:
-Physiotherapy (for mild cases): e.g. heat and ultrasonographic waves, physical therapy, custom splint or brace for finger stretching
-Occupational therapy
Intralesional corticosteroid injection
-Collagenase injection
-Other measures: 5-fluorouracil, imiquimod, botulinum toxin, and hyperbaric oxygen
-Surgery: surgery is indicated if MCP contracture is more than 30° or there is contracture of PIP
A 32-year-old man presents to your office with complaint of low back pain in the setting of ankylosing spondylitis (AS), which he has had for the past 5 years. He has been on treatment with naproxen 500 mg, 3 times a day, for the past few years with no significant improvement. An X-ray of the lumbosacral area is obtained and is shown in the following
photograph. Which one of the following is the most appropriate management option for this patient?
A. Start him on sulfasalazine.
B. Start him on methotrexate.
C. Start him on infliximab.
D. Start him on cyclosporine.
E. Double the dose of naproxen.
C. Start him on infliximab.
Non-steroidal anti-inflammatory drugs (NSAIDs) are first-line therapy for symptomatic patients with AS. Recent studies suggest that regular NSAID use in AS slows radiographic progression more than on-demand use. An individualized assessment of the risk of long-term NSAID use should be made in consultation with the rheumatologist before long-term daily NSAID use is recommended.
Tumour Necrotizing Factor (TNF) inhibitors
such as infliximab are used when there is not adequate response to at least two different NSAIDs. TNF inhibitor therapy has strikingly improved the quality of life in over two-thirds of the patients. These agents are listed on the Pharmaceutical Benefits Scheme (PBS) for active AS not adequately responsive to exercise and NSAIDs, but not for non-radiographic axial AS, meaning that these drugs are not indicated where the X-ray changes of sacroiliitis are absent. Randomized controlled trials, however, suggest better clinical responses in early non-radiographic disease.
This patient has not adequately responded to maximum dose of naproxen (an NSAID). On the other hand, his lumbosacral X-ray shows the classic bamboo spine (squaring and fusion of lumbosacral vertebrae) seen in AS; therefore, he will be an appropriate candidate to be started on infliximab as the most appropriate next step in management.
(Options A and B) Sulfasalazine and methotrexate are not indicated where there is axial involvement.
(Option D) Cyclosporine has not shown effective in management of axial AS.
(Option E) Doubling the dose of naproxen will exceed the maximum dose of this drug and is associated with significant adverse effects and probably no improved outcome.
NOTE - If there was an option suggesting switching to another NSAID, it would be the correct answer because some patients unresponsive to one NSAID may improve on another.
A 68-year-old woman presents to your practice complaining of pain in her right hip. The pain started 2 days ago and has escalated since. She refuses to bear weight on the affected side, as this brings on severe pain. The patient denies any history of osteoarthritis or other joint diseases, but admits to long-term use of oral corticosteroids for Behçet disease. On examination, all movements of the right hip joint are diminished and very painful. Which one of the following would be the most likely diagnosis?
A. Gout.
B. Avascular necrosis of the femoral head.
C. Osteoarthritis of the hip joint.
D. Septic arthritis.
E. Bony metastasis from a primary cancer.
B. Avascular necrosis of the femoral head.
There are many conditions that can cause hip or groin pain in adults. The following 2 are the most common causes in adults:
- A flare of a chronic inflammatory condition such as rheumatoid arthritis
- Degenerative changes of the hip joint, such as in osteoarthritis
Other causes, especially in the elderly may include:
- Fracture of the femoral head or neck
- Degenerative spondylosis of lumbosacral spine (neurogenic claudication)
- Arterial occlusions (vascular claudication)
- Polymyalgia rheumatica
- Trochanteric bursitis
- Bony metastases from a primary cancer
- Atraumatic avascular necrosis of the femoral head
Atraumatic avascular necrosis of the femoral neck, although not a very common condition, should always be suspected in an elderly patient, particularly if the following risk factors are present in the history:
-Long-term steroid use
-Chronic alcohol use and resulting liver disease
-Sickle cell disease
-Past hip fracture
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Of the given options, considering the history of long-term steroid use, avascular necrosis of the femoral head seems more likely.
The initial step in diagnosis would be an X-ray of the hip. Typical finding is variable density of the femoral head.
Sonography can be used to exclude joint effusion due to an acute inflammation such as in a flare up of rheumatoid arthritis or septic arthritis. The most accurate diagnostic tool would be an MRI with characteristic ‘geographic’ subchondral lesions. It is often considered if the diagnosis remains equivocal.
(Option A) Gout can cause acute inflammation and pain of the joint, but the hip joint is unlikely to be affected by this disease.
(Option C) Sudden onset of the hip pain, without any previous history, is a very unlikely to be caused by osteoarthritis (OA) of the hip. The history of OA often includes insidious onset and progression to more severe states over a long period of time.
(Option D) Septic arthritis is a serious condition that can lead to complete joint destruction and permanent disability within hours if untreated, and needs to be excluded; however, it is not the most common diagnosis in this case scenario. The patient with septic arthritis is expected to be more systematically ill, but the range of motions of the affected hip joint
would be painfully limited, just such as this patient.
(Option E) Bony metastases from a primary cancer does not seem to be a likely diagnosis, as a cancer so advanced to metastasize to distant sites, is expected to have presented with sign and symptoms of the primary tumor earlier. The examination is mentioned to be unremarkable otherwise.
A 35-year-old man presents to your GP clinic with severe back pain for several years. The pain is worse on waking up in the morning. Pain and stiffness make him stay in bed for at least 30 minutes. The pain ameliorates by walking and physical activity throughout the day. His condition has deteriorated recently despite being on the maximum dose of naproxen. An X-ray of his lumbosacral spine is shown in the accompanying photograph. Which one of the following would be the most appropriate next step in management?
A. Sulfasalazine.
B. Methotrexate.
C. Adalimumab.
D. Aspirin.
E. Prednisolone.
C. Adalimumab.
The X-ray shows severe deformities of the lumbosacral spine evident by the fusion of vertebrae resulting in the characteristic bamboo spine, a hallmark radiographic feature in ankylosing spondylitis (AS)
.
Non-steroidal anti-inflammatory drugs (NSAIDs) are first-line therapy for symptomatic patients with AS; however, when the disease is rapidly progressive and/or there is not adequate response despite the maximum dose of NSAIDs, biological disease-modifying anti-rheumatic drugs (bDMARDs) are next step in management.
Of these drugs, Tumor Necrotizing Factor (TNF) inhibitors
have strikingly improved the quality of life in more than two-thirds of the patients. These agents are indicated for active AS not adequately responsive to exercise and NSAIDs with radiographic axial AS (as in this case), but not for non-radiographic axial AS, meaning that these drugs are not indicated where the X-ray changes typical for AS are absent. Randomized controlled trials, however, suggest better clinical responses in early non-radiographic disease. Infliximab, etanercept, adalimumab, and golimumab are TNF inhibitors approved for the treatment of AS when indicated.
With inadequate response to NSAIDs and characteristic X-ray findings, this patient is eligible for treatment with adalimumab as the next best step in management.
Traditional DMARDs such as methotrexate, azathioprine, and sulfasalazine have little effect on spinal disease, but can be useful for associated peripheral arthritis. Other biologic agents available for rheumatoid arthritis in Australia have not been effective for the treatment of AS.
(Options A and B) Sulfasalazine and methotrexate are not effective treatments when there is axial involvement.
(Option D) If among the options, a trial of a second NSAID would be the correct answer because one of the criteria required for bDMARD to be covered by the pharmaceutical benefits scheme (PBS) is the failure of at least two NSAIDs before the commencement of bDMARDs. Aspirin is a salicylate, not an NSAID.
(Option E) Systemic steroids may be used for extra-spinal presentations of AS such as uveitis, inflammatory bowel disease (IBD), etc. but are not indicated nor effective for the treatment of spinal involvement
A 51-year-old man presents to your practice for back pain. He was diagnosed with ankylosing spondylitis 20 years ago and has had mild back pain all this time. He had received no
medical treatment and has been on an exercise program on an on-and-off basis. The patient suffers from peptic ulcer disease and has been treated for the condition several times.
Which one of the following is the most appropriate next step in management?
A. Paracetamol.
B. Naproxen.
C. Methotrexate.
D. Sulfasalazine.
E. Infliximab.
Correct Answer Is A
First-line management of ankylosing spondylitis (AS) is NSAIDs. Regular use of NSAIDs has been shown to reduce the symptoms as well as the rate at which skeletal changes
occur. This patient has been diagnosed with AS 20 years ago and has not received any medication. On the other hand, mild low back pain is the patient’s current complaint.
Without gastric problems, NSAIDs (naproxen) was the drug of choice to consider first, but with peptic ulcer disease and because the pain is mild, simple analgesics such as paracetamol should be tried first in an attempt to alleviate the patient’s pain without significantly increasing the risk of his peptic ulcer disease deteriorate.
NOTE - In general, simple analgesics and opioids are considered where there is residual pain despite NSAID use or when NSAIDs are contraindicated.
(Option B) Despite the increased risk, NSAIDs may be considered at the lowest doses possible, once simple analgesics proved ineffective in pain control. COX2-selective NSAIDs
such as celecoxib are preferred over non-selective NSAIDs if the patient does not have cardiovascular or cerebrovascular diseases.
(Options C and D) Methotrexate and sulfasalazine may occasionally be considered for the treatment of extra-spinal manifestation of AS.
(Option E) Infliximab is a tumor necrotizing factor (TNF) inhibitor approved to use in patients with axial involvement with inadequate response to a maximum dose of NSAIDs or in
those with severely progressive disease.
An 80-year-old woman sustains a fall in the bathroom and is brought to the emergency department by her daughter. She has severe pain and decreased range of motion in all
directions in the right hip. The right leg appears shorter than the left and is externally rotated. A bedside portable X-ray of the pelvis is taken which is shown in the following
photograph. Which one of the following is the most appropriate management option for this patient?
A. Intramedullay nail placement.
B. External fixation.
C. Hip arthroplasty.
D. Analgesics and bed rest.
E. Traction.
Correct Answer Is C
The X-ray shows an intracapsular (Garden) fracture of the right femoral neck. The fracture can be subcapital, transcervical, or basicervical. Only such fractures can be considered genuine femoral neck fractures.
Garden classification of intracapsular (subcapital) fractures of the femoral neck is as follows:
Garden type I: incomplete fracture with valgus impaction
Garden type II: Complete fracture without displacement
Garden type III: Complete fracture with partial displacement of the fracture fragments
Garden type IV: Complete fracture with total displacement allowing the femoral head to rotate back to an anatomic position
In reality the distinction between classes is difficult; however, complete fracture and displacement of the femoral head makes Garden type III (or IV) femoral neck fracture the most
likely diagnosis.
Garden types I and II femoral neck fractures are surgically stabilized with closed reduction and internal fixation. Garden types III and IV are controversial in the type of implant used
for treatment. In younger patients, closed or open reduction is recommended. In less active older patients, however, prosthetic replacement is recommended.
None of other options are superior to hip arthroplasty.
Examination of an aspirate from an acutely painful swollen knee is as follows:
White blood cell count: 4100 (<2000μL)
Red blood cells: few
Crystals: negative
Culture: no growth
Which of the following is the most accurate interpretation of the results?
A. Traumatic tap.
B. Inflammation.
C. TB arthritis.
D. Viral arthritis.
E. Gonococcal arthritis.
Correct Answer Is B
Biochemically, the synovial fluid is an ultrafiltrate of plasma across the synovial membrane enriched with various compounds produced by the synoviocytes. In normal physiological conditions, the biochemical composition of
the synovial fluid is similar to that of plasma. In pathological conditions, laboratory evaluation of synovial fluid provides information about the pathology of the disease affecting the joint (e.g., arthritis).
Similar to other body fluids, common laboratory evaluation of synovial fluid includes the following three steps:
Physical examination of synovial fluid (e.g., appearance, including color, viscosity, and other physical characteristics)
Chemical analysis (e.g., glucose, total protein level, uric acid)
Microscopic evaluation (e.g., cell count and differential count, crystal identification)
Based on physical and laboratory findings, synovial fluid can be categorized as:
Normal
Non-inflammatory
Inflammatory
Septic
Hemorrhagic
The following table summarizes the characteristic feature of synovial fluid in different conditions: (See photo)
Although a cell count of 4800 in the aspirate analysis could be seen in both inflammatory and infectious conditions, a very high cell count of >50,000 or even >100,000 is more specific for infectious causes (read the Exam Tip below). Furthermore, a negative culture does not exclude infection but makes it less likely.
In practice, a cell count of 2000-50,000 is the typical finding in inflammatory joint diseases such as rheumatoid arthritis, lupus arthritis, gout, and pseudogout. The absence of crystals, however, makes crystal-induced
inflammation unlikely.
(Option A) Although a traumatic tap results in blood in the synovial fluid, other features such as elevated white cell count are absent unless a concomitant condition is present. A few red blood cells (RBCs) are usually present
even in a normal synovial fluid.
(Option C) In TB arthritis, synovial fluid analysis is usually not helpful. The white cell count can be high or low with the dominance of either neutrophils or lymphocytes and no other specific diagnostic features. In fact, this
aspirate analysis can also be caused by TB as well, yet an inflammatory condition is more likely.
(Option D) Viral arthritis presents with a high white cell count with a predominance of polymorphonuclears (PMNs), but the cultures are negative.
(Option E) A white cell count of 4100, makes gonococcal arthritis less likely. Gonococcal arthritis often presents with a white cell count of 34000-68000
EXAM TIP
Remember the following tips for the exam:
The WBC count of a normal joint aspirate is < 200.
With degenerative diseases (e.g., OA) or trauma, the WBC count of joint fluid is 200-2000.
Typical inflammatory joint fluid either with the crystalline or non-crystalline disease has a WBC of 2000-50,000 (more commonly 5,000-50,000)
The typical WBC count of joint fluid in septic arthritis is usually >50,000; however, septic arthritis should be considered a possibility in every joint aspirate with WBC>5000, especially if the arthritis is monoarticular and
the patient has already received antibiotics.
It is not common for gout and pseudogout to present with WBC>50,000. If so, co-infection is a possibility to consider.
A 37-year-old man is brought to the Emergency Department after he sustained a motor vehicle accident. Upon arrival, a quick review excludes any life-threatening internal injuries.
He has a deformed right leg highly indicative of a fracture. There is a bleeding laceration over the deformity. An X-ray shows fractures of the tibial and fibula. As the initial
management, intravenous fluid and antibiotics are started. Which one of the following is the most appropriate next step in management?
A. External fixation.
B. Internal fixation.
C. Tetanus prophylaxis.
D. Wound debridment.
E. Wound closure.
Correct Answer Is C
The vignette describes a typical case of open fracture of the right leg. Open fractures are characterized by the fracture exposure to the environment trough a breach of the skin and
underlying soft tissue. Such fractures are particularly at increased risk of infection that can compromise the fracture and healing process.
Always follow the following rules in open fractures / dislocations
**Remove any gross contamination off the wound. No provisional irrigation or debridement is performed at this stage.
**Take photographs of the wound and dress it with wet sterile cover (the photographs are taken, so that other treating physicians do not need to uncover the wound to see
it.)
**Give patient analgesic (preferably intravenously to both control the pain and prepare for a reduction in the emergency department). Morphine is a good option.
**By gentle traction, reduce the fracture and correct misalignments as much as possible.
**Start the patient on intravenous prophylactic antibiotics.
**Give the patient tetanus prophylaxis if indicated.
**Obtain X-rays.
**Urgently arrange for transferring the patient to the operating room for surgical wound debridement and definite treatment of the fracture and dislocation.
There is no comment regarding significant misalignment. The patient’s wound should be covered by wet dressing after photographs are taken (if possible). He also has been started
on intravenous antibiotics; therefore, the next best step for him would tetanus prophylaxis if indicated.
(Options A and B) Fixation of fractures is performed in the operating room after surgical irrigation and wound debridement.
(Option D) Wound debridement including surgical removal of all devitalized soft tissues and bone is a crucial step in management of any open fracture/dislocation because
infections may ensue and result in poor outcomes. However, debridement should be performed in the sterile environment of the operating room, not in the non-sterile environment
of the Emergency Department where more exploration of the wound can lead to increased risk of infection.
(Option E) Wound closure can be performed (if not contraindicated such as in highly contaminated wounds or delayed presentation) after vigorous irrigation and debridement of the
wound and fixation of the fracture.
You are visiting a 75-year-old woman in your practice, who is complaining of bilateral pain and stiffness in her shoulders and hips. She explains that the pain and stiffness are worst
on waking, but becomes better after 40 to 60 minutes of physical activity. On examination, there is no remarkable finding except generalized stiffness of her hip and shoulder
girdles. Which of the following investigations is most consistent with the diagnosis?
A. Elevated serum calcium.
B. Elevated erythrocyte sedimentation rate (ESR).
C. Positive rheumatoid factor (RF).
D. Increased serum alkaline phosphatase level.
E. Joint space narrowing and decreased bone density on X-rays of the shoulders and hips.
Correct Answer Is B
Pain and morning stiffness of hip and shoulder girdles taking 40-60 minutes of activity to relieve is consistent with polymyalgia rheumatic as the most likely diagnosis.
Polymyalgia rheumatica is an inflammatory rheumatic condition characterized clinically by aching and morning stiffness in the shoulders, hip girdle, and neck. The condition can be
associated with giant cell (temporal) arteritis (GCA). The 2 disorders are thought to represent different manifestations of a shared disease process.
Polymyalgia rheumatica is almost exclusively a disease of adults over the age of 50, and 2- to 3-times more common in women than men.
The prevalence increases with age and
the average age at diagnosis is over 70 years.
Clinical manifestations of polymyalgia rheumatica include:
**The subacute or chronic onset of aching and morning stiffness in the shoulders, hip girdles, neck, and torso (usually symmetric)
**Morning stiffness that typically lasts more than 30 minutes
**Pain – shoulder pain is more common at presentation (70-95%) than hip and neck (50-70%). The pain is worse with movement
**Decreased range of motion
**Synovitis, tenosynovitis, and bursitis - ~50% of patients can exhibit distal musculoskeletal involvement; some patients may have swelling and pitting edema of the hands,
wrists, ankles, and top of the feet. Tenosynovitis can also cause carpal tunnel syndrome, which occurs in approximately 10 to 15% of patients with polymyalgia rheumatica
**Subjective weakness - Muscle strength is usually normal, but weakness is frequently reported by patients and may be a problem diagnostically due to diminished effort on
examination because of pain, or clinically because of disuse atrophy. Thus, careful testing is required if weakness is reported.
**Systemic manifestations - Up to 40% of patients may have malaise, fatigue, depression, anorexia, weight loss, and fever
NOTE – Muscle tenderness is not a prominent feature despite what the name implies. If present, tenderness is more likely to be due to synovial or bursal inflammation than
muscle involvement.
The most characteristic finding in polymyalgia rheumatica (and giant cell arteritis) is an elevated erythrocyte sedimentation rate (ESR) that is above 40mm/h. According to some
studies, an elevated ESR can be seen in 78-93%. ESR may exceed 100mm/h in some patients.
(Option A) Serum calcium is unaffected in polymyalgia rheumatica.
(Option C) Serologic tests, such as rheumatoid factor (RF), antinuclear antibodies (ANA), and cyclic citrullinated peptide (CCP) antibodies are typically negative.
(Option D) Some patients may have some rise in their liver enzymes, especially alkaline phosphatase; however, this is more common in patients with giant cell arteritis than
polymyalgia rheumatica alone.
(Option E) Joints are not affected in polymyalgia rheumatica. No X-ray abnormalities are expected
References
* UpToDate- Clinical Manifestations and diagnosis of polymyal
A 74-year-old woman presents to the emergency department with sudden-onset left visual loss that occurred within a few hours. She also mentions having left-sided headaches for
the past few days and hip and shoulder pain and stiffness for 7 months. She has tried over-the-counter painkillers for her headache with no response. Which one of the following is
the most appropriate next step in management?
A. Muscle biopsy.
B. CT scan of the head.
C. MRI of the head.
D. Erythrocyte sedimentation rate (ESR).
E. Ocular massage.
Correct Answer Is D
Sudden-onset visual loss and headache in a patient over the age of 50 is very likely to be giant cell (temporal) arteritis until proven otherwise. Additionally, this patient has had hip
and shoulder pain, suggestive of polymyalgia rheumatica as a strong association.
Giant cell arteritis (GCA) and polymyalgia rheumatica are closely associated syndromes with unknown etiology. GCA and polymyalgia rheumatica can develop alone, although in
20% of cases both are present (as in this case)
Polymyalgia rheumatica presents with pain and stiffness of shoulders and/or hips often symmetrically. Neck pain and/or stiffness may be present. Shoulder pain is the presenting
symptom in 70-95% of patients. Hip and/or shoulder pain is present in 50-70% of patients.
Tenosynovitis and bursitis may be present in 50% of patients. A decreased range of
motion can be found on examination. A subjective sense of muscle weakness may be reported by the patient despite the fact that muscles are not involved. Constitutional
symptoms such as fever, weight loss, malaise, fatigue, and anorexia are present in 40% of patients.
GCA presents with headaches often unresponsive or poorly responsive to analgesics, scalp tenderness, jaw claudication, and weak or absent pulsation of the temporal artery. A new headache occurs in at least 2/3 of patients. The headache may have a variety of presentations in GCA, but being new-onset is the critical feature. In its classic form, the headache of GCA is located in temporal regions, but it may also occur in frontal or occipital areas or may be generalized. Headache is the chief complaint in most patients, but in some, it may be absent or elicited by direct questioning.
Systemic symptoms of GCA include fever, fatigue, and weight loss. Up to 50% of patients have a fever that is often low-grade but can exceed 39°C in 15% of patients which can be
mistaken for infection. Importantly, in approximately 10% of patients, constitutional symptoms are the only manifestations of GCA.
NOTE – in patients with polymyalgia rheumatica, ongoing monitoring for symptoms or physical findings suggestive of GCA is recommended. Evaluation including biopsy should be
performed if symptoms of GCA develop, even if patients are on corticosteroids.
Once GCA/polymyalgia rheumatica is suspected on clinical grounds, ESR is the most appropriate next step in management. An elevated ESR above 40mm/h is the most
characteristic finding in GCA/polymyalgia rheumatica. With an elevated ESR, immediate treatment with systemic corticosteroids should be started and a temporal artery biopsy for a
definite diagnosis arranged.
(Option A) Although some patients may complain of muscle pain and tenderness, muscles are not involved in GCA/polymyalgia rheumatica. If present, tenderness is more likely to
be due to synovial or bursal inflammation than muscle involvement. Muscle biopsy has no role in the diagnosis of these conditions.
(Options B and C) Imaging studies such as CT scans or MRIs are not routinely used for diagnosis of GCA/polymyalgia rheumatica unless the diagnosis is equivocal and other
diagnoses are considered.
(Option E) ocular massage is used initially for urgent management of retinal artery occlusion that not the case here
A 76-year-old woman presents with painful and stiff shoulders that she has had for the past 2 months. The stiffness is worse in the morning and improves after 30-60 minutes of
physical activity. She denies headaches, visual problems, or symptoms such as fever or weight loss. Initial laboratory tests results are:
RBC: 5x10^6 cells/mm3 (4.5-6.5x10^6)
Hb:115g/L (130-180)
MCV: 85 fL (76-96)
WCC: 9000 cells/mm3 (N: 4000-11000)
Platelet: 500,000/mm3 (N: 150,000-400,000)
Metabolic panel: normal
ESR: 65mm/h
CRP: Positive
RF: negative
ANA: negative
Which of the following would you consider for treating this patient?
A. Paracetamol.
B. Prednisolone.
C. Antibiotics.
D. Non-steroidal anti-inflammatory drugs (NSAIDs).
E. Physical therapy.
Correct Answer Is B
The painful stiff shoulder and/or hip girdle in a person over the age of 50 years is mostly consistent with polymyalgia rheumatica as the most likely diagnosis.
Polymyalgia rheumatica is an inflammatory rheumatic condition characterized clinically by aching and morning stiffness in the shoulders, hip girdle, and neck. The condition can be
associated with giant cell (temporal) arteritis (GCA). The two disorders are thought to represent different manifestations of a shared disease process.
Polymyalgia rheumatica is almost exclusively a disease of adults over the age of 50, and 2- to 3-times more common in women than men. The prevalence increases with age and
the average age at diagnosis is over 70 years.
Polymyalgia rheumatica presents with pain and stiffness of shoulders and/or hips often symmetrically. Neck pain and/or stiffness may be present. Shoulder pain is the presenting
symptom in 70-95% of patients. Hip and/or neck pain is present in 50-70% of patients. Tenosynovitis and bursitis may be present in 50% of patients. A decreased range of motion
can be found on examination. A subjective sense of muscle weakness may be reported by the patient despite the fact that muscles are not involved. Constitutional symptoms such
as fever, weight loss, malaise, fatigue, and anorexia are present in 40% of patients.
The most characteristic finding in polymyalgia rheumatica (and giant cell arteritis) is an elevated erythrocyte sedimentation rate (ESR) that is above 40mm/h. According to some
studies, an elevated ESR (and CRP) can be seen in 78-93% .ESR may exceed 100mm/h in some patients.
Normocytic normochromic anemia is seen in some patients. WCC is normal, but platelet count can be raised, as platelets are acute phase reactants and can be elevated in
inflammatory conditions. Serologic tests, such as rheumatoid factor (RF), antinuclear antibodies (ANA), and cyclic citrullinated peptide (CCP) antibodies are typically negative.
Some may have an increase in their liver enzymes, especially alkaline phosphatase; however, this is more common in patients with giant cell arteritis than polymyalgia rheumatica
alone.
Corticosteroids are recommended as the initial therapy in patients with polymyalgia rheumatica. The primary objective of treatment is improvement in symptoms. Therapy is mostly
symptomatic and has not been proven to improve prognosis or prevent progression to giant cell arteritis. Most patients experience dramatic improvement in symptoms within days
of therapy.
Prednisone/prednisolone 0-20mg, daily in the morning, is the recommended regimen. Therapy is often required for 2 to 3 years. The minimum duration of therapy is unlikely to be
less than 12 months. Long-term use of corticosteroid use in such patients is associated with corticosteroid-induced bone loss and osteoporosis. Prophylactic calcium/vitamin D
supplementation is recommended and bisphosphonates (e.g. alendronate) may be indicated for prevention.
In patients with CGA, daily doses of 40-60mg are required. The addition of aspirin is recommended. For patients with visual symptoms, who present early, a 3-day course of
intravenous prednisolone, followed by oral therapy is the management of choice.
NOTE – Response to treatment is monitored with ESR and CRP.
(Option A) Polymyalgia rheumatica is an inflammatory condition. Paracetamol is unlikely to be of considerable benefit in patients with polymyalgia rheumatica.
(Option C) Antibiotics have no role in the management of polymyalgia rheumatica and/or GCA.
(Option D) NSAIDs have been tried as corticosteroid-sparing alternatives, but can be associated with significant adverse effects. NSAIDs are occasionally used in patients on very
low doses of corticosteroids, who also require analgesic or anti-inflammatory therapy for other disorders, such as osteoarthritis or rotator cuff tendonitis.
(Option E) Physical therapy is recommended as adjunctive therapy in patients who have difficulty regaining good mobility and a full range of motion despite control of the
inflammatory process.
A 73-year-old woman presents to your practice with a complaint of shoulder pain for the past 8 months. The pain is mostly felt in both shoulders and is aching and vague in nature.
She also has shoulder girdle stiffness in the morning, often taking 30-60 minutes of physical activity and sometimes a hot bath to improve. She denies any fever, weight loss,
headache, or visual symptoms. Past medical history is significant for osteoporosis, for which she is on alendronate and supplemental calcium and vitamin D. Laboratory tests show
normocytic, normochromic anemia and an erythrocyte sedimentation rate (ESR) of 100mm/h. Which one of the following is the most appropriate next step in management?
A. Corticosteroids.
B. Non-steroidal anti-inflammatory drugs (NSAIDs).
C. Paracetamol.
D. Methotrexate.
E. Infliximab.
Correct Answer Is A
The clinical picture is highly suggestive of polymyalgia rheumatica an inflammatory disease of uncertain etiology that can be associated with giant cell arteritis in some patients. If both conditions are present polymyalgia rheumatica invariably precedes GCA.
As in this patient, polymyalgia rheumatica presents with pain and stiffness of the shoulders and hips in a symmetrical fashion. The cervical spine may be involved. There is marked stiffness usually early in the morning. The symptoms tend to subside or at least relieve by the end of the day. Constitutional symptoms such as malaise, low-grade fever, anorexia, and weight loss may be present in 40% of patients.
Corticosteroids are recommended as the initial therapy in patients with polymyalgia rheumatica. The primary objective of treatment is the improvement in symptoms.
Prednisone/prednisolone 10-20mg, daily in the morning is the recommended regimen. Therapy is often required for 2 to 3 years. The minimum duration of therapy is unlikely to be
less than 12 months. Long-term use of corticosteroid use in such patients is associated with corticosteroid-induced bone loss and osteoporosis. In this patient with pre-existing
osteoporosis, long-term corticosteroid therapy may result in the deterioration of bone loss; nonetheless, there is no alternative effective therapy for myalgia rheumatica to replace
corticosteroids.
This patient should also be started on preventive measures to decrease the adverse effects of corticosteroids on bone, if the duration of therapy is predicted to exceed one month:
**Weight-bearing exercises where possible
**Adequate calcium intake
**Measurement and addition of vitamin D if indicated
**Monitoring bone density from the outset of therapy
**Bisphosphonates if indicated
(Option B) NSAIDs have been tried as corticosteroid-sparing alternatives, but can be associated with significant adverse effects. NSAIDs are occasionally used in patients on very low doses of corticosteroids who also require analgesic or anti-inflammatory therapy for other disorders, such as osteoarthritis or rotator cuff tendonitis. NSAIDs alone are unlikely to be useful for the treatment of polymyalgia rheumatica.
(Option C) Polymyalgia rheumatica is an inflammatory condition. Paracetamol is unlikely to be of considerable benefit in patients with polymyalgia rheumatica.
(Option D) Methotrexate alone is not shown to be effective in managing polymyalgia rheumatica Addition of methotrexate to corticosteroids may be used to reduce the dose of corticosteroids in patients who are at increased risk of corticosteroid-induced adverse effects such as osteopenia/osteoporosis. This has been suggested by some but not all
studies. In general, methotrexate is rarely used in patients with polymyalgia rheumatica without GCA, because low doses of corticosteroids are often sufficient to control the
disease.
(Option E) The use of TNF inhibitors, such as infliximab and etanercept, is effective in the treatment of polymyalgia rheumatica as an alternative to corticosteroids
A 70-year-old man presents with complaints of headache and blurry vision in his right eye. He also mentions a history of shoulder pain that has been bilateral and associated with
morning stiffness of at least 30 minutes for the past few months. Which one of the following investigations is most important to establish the diagnosis?
A. Erythrocyte sedimentation rate (ESR).
B. ANA.
C. Temporal artery biopsy.
D. CT scan of the head.
E. Evoked visual potential.
Correct Answer Is C
The clinical picture of headache and visual impairment in a patient over the age of 50 is highly suggestive of giant cell arteritis. The preceding history of shoulder pain and stiffness
indicates polymyalgia rheumatica and makes the diagnosis more certain.
When CGA is suspected the initial step is measuring the erythrocyte sedimentation rate (ESR). An elevated ESR is the most characteristic finding in patients with GCA/polymyalgia
rheumatica. An ESR level of less than 40mm/h makes CGA/polymyalgia rheumatica an unlikely diagnosis while measurings above 40mm/h prompt treatment with corticosteroids to
prevent permanent visual loss. Arrangements then should be made to perform a temporal artery biopsy. Superficial temporal artery biopsy is the criterion standard for diagnosis
of CGA and should be obtained almost without exception in patients with suspected GCA on clinical grounds. It is essential because the treatment course for GCA is long and often
complicated, and many of the nonspecific symptoms of GCA such as headache, body aches, and fatigue may occur in many other diseases. A positive temporal artery biopsy is
100% specific but has a relatively low sensitivity of 15-40% for the diagnosis of GCA.
NOTE - Patients who only have the symptoms of polymyalgia rheumatica do not need a biopsy. However, such patients should be carefully questioned about headache, jaw or
arm claudication, visual symptoms, and any unusual pain in the face, throat, or tongue. Any of these symptoms suggest the possibility of GCA.
(Option B) ESR is performed to determine if prompt treatment with corticosteroids should be started. It is not diagnostic for CGA.
(Option C) Serologic tests, such as rheumatoid factor (RF), antinuclear antibodies (ANA), and cyclic citrullinated peptide (CCP) antibodies are typically negative, and not used for
diagnosis of CGA.
(Option D) Imaging studies such as CT scans are not routinely used to diagnose GCA unless another diagnosis is considered.
(Option E) Evoked visual potentials test is used for the diagnosis of optic neuritis and is not indicated here.
Mr. Johnson comes to your practice, complaining of progressively increasing left knee pain. He is 67 years old and otherwise healthy. He elaborates that the pain is brought on by walking. Generally, he feels well in the morning except for the stiffness of the left knee which often resolves within minutes of physical activity. When he starts walking, the pain is
brought on and builds up to a maximum intensity throughout the day. On physical examination, everything is normal except the crepitations of the left knee. The knee is not tender or warm to the touch and there is no swelling either. You order an X-ray of the left knee. Which one of the following would be the least likely finding on the X-ray?
A. Joint space narrowing.
B. Subchondral cysts.
C. Periarticular osteoporosis.
D. Osteophytes.
E. Increased density of bone ends.
Correct Answer Is C
This patient’s clinical presentation fits the diagnosis of osteoarthritis of the left knee. Osteoarthritis is the most common arthropathy worldwide.
The diagnosis of OA is mainly clinical. An X-ray of the affected joint is necessary to confirm the diagnosis. The characteristic findings on X-ray of an osteoarthritic joint are:
**Joint space narrowing
**Presence of subchondral cysts
**Sclerosis of subchondral bone
**Osteophytes at the outer edges of the joint lines
The pathophysiology of the disease includes chronic destruction of bone cartilage. With the diminished protective function of the cartilage, the periarticular bone undergoes repetitive trauma leading to bone destruction, which is followed by abnormal bone formation in form of bony spurs also called osteophytes.
Osteophyte formation plays a major role in the pathophysiology of pain in OA.
The healing process is affected by bony areas leads to sclerosis of the bony edges of the joint, signified by hyperdense sclerotic subchondral bones. Joint destruction and degeneration lead to joint space narrowing. Subchondral cyst formation would be another finding.
Osteopenia or osteoporosis around the joint is seen in inflammatory conditions such as rheumatoid arthritis or neuropathic arthropathy.
Neuropathic arthropathy (Charcot’s joint) may be seen in the following conditions:
**Diabetes mellitus neuropathy – is the most common cause in Australia and worldwide. It is related to long-term poor blood glucose control.
**Alcohol neuropathy
**Cerebral palsy
**Leprosy
**Syphilis (tabes dorsalis)
**Spinal cord injury
**Myelomeningocele
**Syringomyelia
**Intra-articular steroid injection
**Congenital insensitivity to pain
**Peroneal muscular atrophy
The classic findings on an X-ray of a joint with neuropathic arthropathy would be:
**Juxta-articular osteopenia
**Joint space narrowing
Osteopenia/osteoporosis around the joint (juxta-articular) is unlikely to be seen in OA.
A 17-year-old boy falls on his outstretched right arm, with subsequent shoulder pain and limited movement of his right shoulder, especially when attempting to elevate his arm over
the head. His appearance is illustrated in the following photograph. Which one of the following is the most likely diagnosis?
A. Fracture of the surgical neck of humerus.
B. Rupture of the rotator cuff tendon.
C. Dislocated glenohumeral joint.
D. Rupture of the long head of biceps tendon.
E. Dislocated acromioclavicular joint.
Correct Answer Is C
The flattened shoulder, as well as the way the patient is holding the affected arm to limit shoulder for preventing pain is typical for anterior glenohumeral dislocation.
Shoulder dislocations account for 50% of all major joint dislocations. In over 90% of cases, such dislocation occurs anteriorly. Posterior, inferior, or superior dislocations account for
the remaining 10%.
An anterior shoulder dislocation is usually caused by a blow to the abducted, externally rotated, and extended arm (e.g. blocking a basketball shot). Less commonly, a blow to the
posterior humerus or a fall on an outstretched arm may cause an anterior dislocation.
An anteriorly dislocated shoulder causes the arm to be slightly abducted and externally rotated. The patient resists all movement. There is loss of the normal round appearance of
the shoulder resulting in a flat shoulder as seen in the photograph.
(Option A) Fracture of the surgical neck of the humerus does not cause a flat shoulder. Pain and tenderness are almost always present. Bruising, swelling, or deformity may occur.
(Option B) Rotator cuff ruptures does not cause the shoulder to become flat. Pain and varying inability to abduct the arm are characteristic features.
(Option D) Rupture of the long head of the biceps tendon does not cause a flattened shoulder. Resisted flexion can elicit pain in the antecubital fossa. On forearm flexion, the bulk of the contracted biceps is lower than the unaffected arm.
(Option E) Acromioclavicular (AC) joint dislocation causes pain, tenderness and the classic step deformity in the AC joint. Arm raise is limited due to exquisite pain when attempted.
A young man presents to the emergency department after injuring his shoulder in a fall. His X-ray is shown in the following photograph. Testing the motor function by resisted
isometric contraction of which one of the following muscles would be most likely to confirm the presence of an associated nerve injury?
A. Latissimus dorsi.
B. Pectoralis major.
C. Trapezius.
D. Serratus anterior.
E. Deltoid
Correct Answer Is E
Significant findings on this X-ray of the shoudler are a humeral head out of the glenoid fossa and displaced inferiorly. These findings are typical for anterior dislocation of the
glenohumeral joint.
Shoulder dislocations often result in injury of the axillary nerve. Axillary nerve runs inferiorly to the humeral head and wraps around the surgical neck of the humerus. Axillary nerve
innervates the deltoid and terese minor muscles and the skin of the lateral shoulder (shoulder badge region). Axillary nerve dysfunction manifests as loss of sensation in a ‘shoulder badge’ distribution and deltoid muscle weakness. It is impractical to ask the patient to move the affected arm due to pain; however, in the presence of axillary nerve injury, the patient is often unable to isometrically contracts the deltoid muscle.
No other muscle mentioned in the options are innervated by the axillary nerve; hence, unaffected by axially nerve injury.
A patient with anterior dislocation of the shoulder is unable to perform which one of the following actions?
A. Turning the door knob.
B. Combing hair.
C. Taking a knife from the table.
D. Shaking hand.
E. Wrist extension.
Correct Answer Is B
Shoulder dislocation often result in injury of the axillary nerve. Axillary nerve runs inferiorly to the humeral head and wraps around the surgical neck of the humerus. Axillary nerve
innervates the deltoid and terese minor muscles and the skin of the lateral shoulder (shoulder badge region) Axillary nerve dysfunction manifests as loss of sensation in a ‘shoulder badge’ distribution and deltoid muscle weakness. Even in the absence of such injury, a patient with anterior shoulder dislocation cannot raise the arm; hence not able to comb hair.
Patients with anterior shoulder dislocation can use their elbow, wrists and fingers, so they can grasp and turn the door knob, pick and hold objects with their hand, shake hand or
extend the wrist.