Bisphosphonates, particularly alendronate, are the recommended treatment for fragility fractures in postmenopausal women. Additionally, calcium and vitamin D supplementation should be considered, along with lifestyle advice on nutrition, exercise, and fall prevention.

Bisphosphonates: Uses, Adverse Effects, and Patient Counselling

Bisphosphonates are drugs that mimic the action of pyrophosphate, a molecule that helps prevent bone demineralization. They work by inhibiting osteoclasts, the cells responsible for breaking down bone tissue. Bisphosphonates are commonly used to prevent and treat osteoporosis, hypercalcemia, Paget’s disease, and pain from bone metastases.

However, bisphosphonates can cause adverse effects such as oesophageal reactions, osteonecrosis of the jaw, and an increased risk of atypical stress fractures of the proximal femoral shaft in patients taking alendronate. Patients may also experience an acute phase response, which includes fever, myalgia, and arthralgia following administration. Hypocalcemia may also occur due to reduced calcium efflux from bone, but this is usually clinically unimportant.

To minimize the risk of adverse effects, patients taking oral bisphosphonates should swallow the tablets whole with plenty of water while sitting or standing. They should take the medication on an empty stomach at least 30 minutes before breakfast or another oral medication and remain upright for at least 30 minutes after taking the tablet. Hypocalcemia and vitamin D deficiency should be corrected before starting bisphosphonate treatment. However, calcium supplements should only be prescribed if dietary intake is inadequate when starting bisphosphonate treatment for osteoporosis. Vitamin D supplements are usually given.

The duration of bisphosphonate treatment varies depending on the level of risk. Some experts recommend stopping bisphosphonates after five years if the patient is under 75 years old, has a femoral neck T-score of more than -2.5, and is at low risk according to FRAX/NOGG.

The presence of a Codman triangle on an X-ray is a strong indication of osteosarcoma, a bone tumor that can cause night pain and is unresponsive to analgesics. This condition is often associated with Paget disease of the bone, which increases the risk of developing osteosarcoma. Giant cell tumor is another bone tumor that can occur in young adults and has a characteristic ‘soap bubble’ appearance on X-ray. Osteochondroma is a common benign bone tumor that can rarely transform into a malignant chondrosarcoma. Osteoarthritis is a painful joint condition caused by mechanical destruction of the cartilage, often worsened by factors such as obesity and age. Treatment options for osteoarthritis include pain relief medication and joint replacement surgery.

Types of Bone Tumours

Benign and malignant bone tumours are two types of bone tumours. Benign bone tumours are non-cancerous and do not spread to other parts of the body. Osteoma is a benign overgrowth of bone that usually occurs on the skull and is associated with Gardner’s syndrome. Osteochondroma, the most common benign bone tumour, is a cartilage-capped bony projection on the external surface of a bone. Giant cell tumour is a tumour of multinucleated giant cells within a fibrous stroma that occurs most frequently in the epiphyses of long bones.

Malignant bone tumours are cancerous and can spread to other parts of the body. Osteosarcoma is the most common primary malignant bone tumour that mainly affects children and adolescents. It occurs most frequently in the metaphyseal region of long bones prior to epiphyseal closure. Ewing’s sarcoma is a small round blue cell tumour that mainly affects children and adolescents. It occurs most frequently in the pelvis and long bones and is associated with t(11;22) translocation. Chondrosarcoma is a malignant tumour of cartilage that most commonly affects the axial skeleton and is more common in middle-age.

The anterior tibial artery continues as the dorsalis pedis.

The foot has two arches: the longitudinal arch and the transverse arch. The longitudinal arch is higher on the medial side and is supported by the posterior pillar of the calcaneum and the anterior pillar composed of the navicular bone, three cuneiforms, and the medial three metatarsal bones. The transverse arch is located on the anterior part of the tarsus and the posterior part of the metatarsus. The foot has several intertarsal joints, including the sub talar joint, talocalcaneonavicular joint, calcaneocuboid joint, transverse tarsal joint, cuneonavicular joint, intercuneiform joints, and cuneocuboid joint. The foot also has various ligaments, including those of the ankle joint and foot. The foot is innervated by the lateral plantar nerve and medial plantar nerve, and it receives blood supply from the plantar arteries and dorsalis pedis artery. The foot has several muscles, including the abductor hallucis, flexor digitorum brevis, abductor digit minimi, flexor hallucis brevis, adductor hallucis, and extensor digitorum brevis.

The patient is experiencing acute inflammatory arthritis, which is likely caused by pseudogout. This condition occurs when calcium pyrophosphate dihydrate crystals are deposited in the synovial fluid, and it is often associated with chronic hypercalcemia resulting from primary hyperparathyroidism. Pseudogout typically affects the knee joint, and the presence of rhomboid-shaped calcium pyrophosphate crystals in the synovial fluid is diagnostic. Calcium hydroxyapatite crystals are typically found in tendons, while calcium oxalate is the most common component of renal calculi. Xanthomas refer to the deposition of cholesterol and other lipids in soft tissues, while gout is characterized by the deposition of monosodium urate in joints and soft tissues.

Understanding Pseudogout

Pseudogout, also known as acute calcium pyrophosphate crystal deposition disease, is a type of microcrystal synovitis that occurs when calcium pyrophosphate dihydrate crystals are deposited in the synovium. This condition is commonly associated with increasing age, but younger patients who develop pseudogout usually have an underlying risk factor such as haemochromatosis, hyperparathyroidism, low magnesium or phosphate levels, acromegaly, or Wilson’s disease.

The knee, wrist, and shoulders are the most commonly affected joints in pseudogout. Diagnosis is made through joint aspiration, which reveals weakly-positively birefringent rhomboid-shaped crystals, and x-rays, which show chondrocalcinosis. In the knee, linear calcifications of the meniscus and articular cartilage can be seen.

Management of pseudogout involves joint fluid aspiration to rule out septic arthritis, followed by treatment with NSAIDs or intra-articular, intra-muscular, or oral steroids, similar to the treatment for gout. Understanding the risk factors and symptoms of pseudogout can help with early diagnosis and effective management of this condition.

Understanding Perthes’ Disease

Perthes’ disease is a condition that affects the hip joints of children between the ages of 4-8 years. It is caused by a lack of blood supply to the femoral head, leading to bone infarction and degeneration. Boys are five times more likely to develop this condition, and around 10% of cases are bilateral. Symptoms include hip pain, limping, stiffness, and reduced range of hip movement. Early changes can be seen on x-rays, such as widening of the joint space, while later changes include decreased femoral head size and flattening.

Diagnosis is typically made through a plain x-ray, but a technetium bone scan or magnetic resonance imaging may be necessary if symptoms persist despite a normal x-ray. Complications of Perthes’ disease can include osteoarthritis and premature fusion of the growth plates.

The Catterall staging system is used to classify the severity of the disease, with Stage 1 being the mildest and Stage 4 being the most severe. Management options include casting or bracing to keep the femoral head within the acetabulum, observation for children under 6 years old, and surgical intervention for severe deformities in older children.

Overall, most cases of Perthes’ disease will resolve with conservative management, and early diagnosis can improve outcomes. It is important for parents and healthcare providers to be aware of the symptoms and seek medical attention if they suspect a child may be affected by this condition.

Understanding Erythrocyte Sedimentation Rate (ESR)

The Erythrocyte Sedimentation Rate (ESR) is a test that measures the rate at which red blood cells settle in a tube over a period of time. It is a non-specific marker of inflammation and can be affected by various factors such as the size, shape, and number of red blood cells, as well as the concentration of plasma proteins like fibrinogen, alpha2-globulins, and gamma globulins.

A high ESR can be caused by various conditions such as temporal arteritis, myeloma, connective tissue disorders like systemic lupus erythematosus, malignancies, infections, and other factors like increasing age, female sex, and anaemia. On the other hand, a low ESR can be caused by conditions like polycythaemia, afibrinogenaemia, or hypofibrinogenaemia.

It is important to note that while a high ESR can indicate the presence of an underlying condition, it is not a definitive diagnosis and further testing may be required to determine the cause. Therefore, it is essential to consult a healthcare professional for proper evaluation and management.

Adductor Longus Muscle

The adductor longus muscle originates from the anterior body of the pubis and inserts into the middle third of the linea aspera. Its main function is to adduct and flex the thigh, as well as medially rotate the hip. This muscle is innervated by the anterior division of the obturator nerve, which originates from the spinal nerves L2, L3, and L4. The adductor longus is one of the adductor muscles, which are a group of muscles located in the thigh that work together to bring the legs towards the midline of the body. The schematic image below illustrates the relationship of the adductor muscles.

The deltoid muscle is responsible for shoulder abduction and is innervated by the axillary nerve, which originates from the C5 and C6 nerve roots. Compression of this nerve can result in limited ability to raise the affected arm beyond 15 degrees and loss of sensation in the skin overlying the inferior deltoid muscle. Common causes of axillary nerve injury include shoulder dislocation, humeral neck fracture, and shoulder surgery.

In contrast, median nerve palsy typically presents with symptoms of carpal tunnel syndrome or weakness and sensory loss in the forearm and hand, rather than the shoulder and upper arm. Musculocutaneous nerve damage is rare and usually occurs due to direct injury to the axilla. Signs of this type of nerve damage include weakened flexion at the shoulder and elbow, weakened supination of the forearm, and loss of sensation over the lateral forearm.

The radial nerve is responsible for innervating much of the posterior arm and forearm, and symptoms of radial nerve damage depend on the location of the injury. Suprascapular nerve damage may also affect shoulder abduction, but other shoulder movements are typically affected as well.

Upper limb anatomy is a common topic in examinations, and it is important to know certain facts about the nerves and muscles involved. The musculocutaneous nerve is responsible for elbow flexion and supination, and typically only injured as part of a brachial plexus injury. The axillary nerve controls shoulder abduction and can be damaged in cases of humeral neck fracture or dislocation, resulting in a flattened deltoid. The radial nerve is responsible for extension in the forearm, wrist, fingers, and thumb, and can be damaged in cases of humeral midshaft fracture, resulting in wrist drop. The median nerve controls the LOAF muscles and can be damaged in cases of carpal tunnel syndrome or elbow injury. The ulnar nerve controls wrist flexion and can be damaged in cases of medial epicondyle fracture, resulting in a claw hand. The long thoracic nerve controls the serratus anterior and can be damaged during sports or as a complication of mastectomy, resulting in a winged scapula. The brachial plexus can also be damaged, resulting in Erb-Duchenne palsy or Klumpke injury, which can cause the arm to hang by the side and be internally rotated or associated with Horner’s syndrome, respectively.

Mefenamic acid is classified as an NSAID because it works by inhibiting COX, which ultimately leads to a decrease in prostaglandin production. Any response indicating an increase or alteration in prostaglandin levels would be inaccurate. The idea of blocking dorsal horn sodium channels is more characteristic of a neuropathic medication rather than an NSAID.

Understanding Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) and COX-2 Selective NSAIDs

Non-steroidal anti-inflammatory drugs (NSAIDs) are medications that work by inhibiting the activity of cyclooxygenase enzymes, which are responsible for producing key mediators involved in inflammation such as prostaglandins. By reducing the production of these mediators, NSAIDs can help alleviate pain and reduce inflammation. Examples of NSAIDs include ibuprofen, diclofenac, naproxen, and aspirin.

However, NSAIDs can also have important and common side-effects, such as peptic ulceration and exacerbation of asthma. To address these concerns, COX-2 selective NSAIDs were developed. These medications were designed to reduce the incidence of side-effects seen with traditional NSAIDs, particularly peptic ulceration. Examples of COX-2 selective NSAIDs include celecoxib and etoricoxib.

Despite their potential benefits, COX-2 selective NSAIDs are not widely used due to ongoing concerns about cardiovascular safety. This led to the withdrawal of rofecoxib (‘Vioxx’) in 2004. As with any medication, it is important to discuss the potential risks and benefits of NSAIDs and COX-2 selective NSAIDs with a healthcare provider before use.

It is not recommended to partially sample suspicious naevi as this can greatly compromise the accuracy of histological interpretation. Complete excision is necessary for lesions that meet diagnostic criteria. However, it may be acceptable to delay wide excision for margins until definitive histology results are available.

When dealing with suspicious melanomas, it is important to excise them with complete margins. Radical excision is not typically performed for diagnostic purposes, so if subsequent histopathological analysis confirms the presence of melanoma, further excision of margins may be necessary. Incisional punch biopsies of potential melanomas can make histological interpretation challenging and should be avoided whenever possible.

Malignant melanoma is a type of skin cancer that has four main subtypes: superficial spreading, nodular, lentigo maligna, and acral lentiginous. Nodular melanoma is the most aggressive, while the other forms spread more slowly. Superficial spreading melanoma typically affects young people on sun-exposed areas such as the arms, legs, back, and chest. Nodular melanoma appears as a red or black lump that bleeds or oozes and affects middle-aged people. Lentigo maligna affects chronically sun-exposed skin in older people, while acral lentiginous melanoma appears on nails, palms, or soles in people with darker skin pigmentation. Other rare forms of melanoma include desmoplastic melanoma, amelanotic melanoma, and melanoma arising in other parts of the body such as ocular melanoma.

The main diagnostic features of melanoma are changes in size, shape, and color. Secondary features include a diameter of 7mm or more, inflammation, oozing or bleeding, and altered sensation. Suspicious lesions should undergo excision biopsy, and the lesion should be completely removed to facilitate subsequent histopathological assessment. Once the diagnosis is confirmed, the pathology report should be reviewed to determine whether further re-excision of margins is required. The margins of excision are related to Breslow thickness, with lesions 0-1mm thick requiring a margin of 1 cm, lesions 1-2mm thick requiring a margin of 1-2 cm (depending on site and pathological features), lesions 2-4mm thick requiring a margin of 2-3 cm (depending on site and pathological features), and lesions over 4mm thick requiring a margin of 3 cm. Further treatments such as sentinel lymph node mapping, isolated limb perfusion, and block dissection of regional lymph node groups should be selectively applied.