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What's New: Bone and Metabolism

The Bone and Metabolism guidelines have been extensively revised. Major changes to the guidelines are listed below.

New topics


Osteoporosis and minimal-trauma fracture

Key updates in Osteoporosis and minimal-trauma fracture management include:

Vitamin D deficiency

Key updates to Vitamin D defincey in adults include:
  • Clarification on the role of supplementation in patients at risk of deficiency, and treatment in those with confirmed deficiency.
  • Clarified treatment regimens based on severity of deficiency.
  • New treatment regimens for pregnant or breastfeeding adults.
  • Which infants and children should be screened for vitamin D deficiency.
  • Prevention and treatment strategies for vitamin D deficiency and nutritional rickets.
  • The role of vitamin D supplementation.

Thyroid disorders

Approach to diagnosis of thyroid function disorders

Transient thyroid function disorders

The new topic Transient thyroid function disorders groups specific new and existing topics by the self-resolving nature of the disorders, including:

Hypothyroidism

The diagnosis and management of hypothyroidism, has been updated, including:

Thyrotoxicosis and hyperthyroidism

Thyroid disorders and pregnancy

Thyroid disorders and pregnancy is a new topic bringing together extensive revisions to:
Three new algorithms provide quick-reference guidance for thyroid function testing preconception, and management of hypothyroidism, and hyperthyroidism during preconception and pregnancy.

Levothyroxine therapy and long-term follow up for thyroid cancer

Levothyroxine therapy and long-term follow up for thyroid cancer has expanded in response to recommendations from international guidelines that primary care practitioners are well-placed to manage long-term follow up of individuals who have been treated for thyroid cancer and are at low risk of recurrence. The topic offers practical advice for primary care practitioners including:

Adrenal disorders

Adrenal insufficiency: Glucocorticoid replacement during intercurrent illness and surgery

Advice on adjusting glucocorticoid regimens in people with adrenal insufficiency during intercurrent illness and surgery has been expanded and aligned with national and international guidelines. Key updates include:

Adrenal crisis

Key updates in managing adrenal crisis are:
  • an increased emphasis on treating individuals with suspected adrenal crisis immediately in the prehospital setting, then transferring to hospital
  • glucocorticoid recommendations for suspected adrenal crisis in adults and in children are aligned with national and international guidelines.
  • intravenous or intramuscular injection of glucocorticoid is preferred for the emergency management of suspected adrenal crisis in adults ; subcutaneous injection, or oral glucocorticoid, may also be used as an interim measure prehospital or before paramedics arrive.
  • intravenous or intramuscular injection of emergency glucocorticoid is used for children with suspected adrenal crisis
  • emergency intravenous glucose regimens are included for hypoglycaemia associated with adrenal crisis
  • .

Management for adrenal insufficiency during pregnancy and lactation

Advice on adrenal insufficiency during pregnancy and lactation has been expanded, with distinct approaches to management for individuals with pre-existing adrenal insufficiency and new-onset or previously undiagnosed adrenal insufficiency.
Key changes include:

Glucocorticoid-induced adrenal insufficiency (adrenocortical suppression)

Glucocorticoid-induced adrenal insufficiency is the new preferred terminology (previously adrenocortical suppression). A comparative table of glucocorticoidd duration of effect has been expanded to include all systemic glucocorticoids used in Australia.

Primary aldosteronism

Key updates to Primary aldosteronism include:

Osilodrostat for Cushing syndrome

Osilodrostat is a new pharmacological treatment for Cushing syndromebut use is limited to specialists.

Phaeochromocytoma and paraganglioma

Paragangliomas are differentiated from phaeochromocytomas as the clinical presentations, investigations and management vary significantly. Management for both requires a specialist and multidisciplinary approach. Information on factors that may cause a false-positive result on metanephrine screening has been simplified. Genetic testing within families, and lifelong surveillance for metastatic disease, are important.

Calcium disorders

Hypocalcaemia

Key updates to Hypocalcaemia include:
  • serum calcium concentration ranges should be interpreted in the context of clinical presentation, likely aetiology and rate of calcium decrease
  • administration of intravenous calcium for acute severe hypocalcaemia is complex. For clarity and safety, intravenous calcium regimens are divided into regimens for adults and children.

Hypercalcaemia

Key updates to Hypercalcaemia include:

Parathyroid disorders

Hypoparathyroidism

A new topic has been developed on hypoparathyroidism covering:
  • the approach to management.
  • management for chronic hypoparathyroidism in adults.
  • management considerations during pregnancy.
  • brief advice on the specialist management of children with hypoparathyroidism.

Hyperparathyroidism

Expanded information on hyperparathyroidism is included covering signs and symptoms, and the role of surgical and pharmacological management.

Hypophosphataemia

Expanded content has been developed to address the different causes of hypophosphataemia:

Pituitary disorders

Chronic hypopituitarism

Updates to Chronic hypopituitarism include:

Acute hypopituitarism

Expanded content on acute hypopituitarism is included, with:

Pituitary apoplexy

Emergency treatment advice for adults with pituitary apoplexy has been updated, including alternative routes of administration, if intravenous access is not possible.

Acromegaly

Updates to Acromegaly include:
  • updated management advice on treatment targets and the role of surgery, drug therapy and radiation therapy.
  • new advice on managing comorbidities associated with acromegaly.

Cushing disease

New advice is included on the specialist use of drug therapy for Cushing disease, outlining the role of osilodrostat, metyrapone and ketoconazole.

Hypophysitis

Expanded advice has been developed on hypophysitis , including a new table outlining types and aetiologies of hypophysitis.

Short stature in children

New advice on the specialist management of achondroplasia has been included.

Osteogenesis imperfecta

Osteogenesis imperfecta has been expanded to mention emerging treatment, such as sclerostin-inhibitor therapy. As more people with osteogenesis imperfecta are reaching adulthood, new sections discussing management in adult and during pregnancy have been added.

Osteomalacia

Osteomalacia focusses on management of osteomalacia caused by vitamin D deficiency, given the separate content now available on osteomalacia secondary to chronic kidney disease–mineral and bone disorder

Rickets

Rickets has been updated and expanded to emphasise the differences between nutritional rickets, chronic kidney disease–mineral and bone disorder, hypophosphataemic rickets and vitamin D-dependent rickets types 1 and 2.


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