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Table of Contents
Northern Lincolnshire and Goole NHS Foundation Trust - Nuclear Medicine
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SOP Code | Title | Review Date |
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REF001 | Bone Scan | 2027-11-04 |
Authorised By | Authorisation Signature (only on master paper copy) | Date Authorised |
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Prof G Avery | 2021-04-20 |
REF001 - Bone Scan
Purpose
The purpose of this document is to assist clinicians in deciding on the appropriateness of a Nuclear Medicine bone scan and to give guidance on the mechanism of referral.
Background
The bone scan a sensitive method for demonstrating disease in bone, often providing earlier diagnosis or demonstrating more lesions than are found on X-ray. It can be used to investigate a wide variety of conditions, both benign and malignant, in adults and children. It is a non-specific investigation and any lesion in bone such as fracture, infection, tumour or healing bone will show as an area of increased radiopharmaceutical accumulation. In many clinical situations, however, the anatomical distribution of the radiopharmaceutical combined with the clinical history or radiographs will suggest a specific diagnosis.
Phosphate analogues are now widely used for bone imaging, having a high localisation in bone and fairly rapid blood clearance from soft tissues. The radiopharmaceutical used locally is Tc99m labelled disodium oxidronate (HDP). The uptake of radiopharmaceutical in bone is related to a number of factors, the most important of which are the blood supply and the rate of bone turnover. Other factors include the quantity of mineralised bone, capillary permeability and the fluid pressure within bone. The phosphates bind to bone first by adsorption on to the bone, followed by binding to the crystalline lattice and organic matrix. The bone scan therefore provides a functional display of skeletal activity. As functional change in bone occurs earlier than structural change, the bone scan, as stated above, will often detect abnormalities before they are seen on X-ray.
Delayed images are usually acquired between 2 and 4 hours after administration of the radiopharmaceutical. When infection of a bone or joint is suspected, or when an assessment of blood flow is required, a three phase investigation can be performed. This involves a dynamic flow study of the area of interest with rapid sequential images taken at the time of radiopharmaceutical administration. Dynamic images are followed by static images of the areas of interest at approximately 5 minutes after administration. These demonstrate the blood pool in normal soft tissue and any hyperaemic areas in bones, joints or soft tissue. Conventional delayed images are then acquired between 2 and 4 hours after administration.
ARSAC Licence Holders |
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Prof Ged Avery |
Dr Najeeb Ahmed |
Typical Radiation Dose (mSv) | ~2.4-4 |
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Staff Permitted to Refer
- Any clinician holding a current valid medical qualification currently employed in Primary or Secondary care.
Referring clinicians are reminded of the requirement to avoid unnecessary exposure to ionising radiation. The investigation may already have been requested at this hospital or elsewhere and clinicians are asked to be particularly vigilant to ensure that their request is not a double request.
Acceptance of Referrals
Requests will only be accepted if the diagnostic question fulfills one of the referral criteria below. Appropriate clinical information must be supplied to allow the investigation to be justified. It is not acceptable to simply request the investigation without appropriate clinical information.
Requests will be returned to the referrer if:
- The diagnostic question is unclear.
- The diagnostic question cannot be answered by the investigation.
- Insufficient clinical information is supplied to justify the investigation.
Requests should be submitted on the orange stripe NUCLEAR MEDICINE (ISOTOPE SCAN) request form. Patient details, Investigation required and Reason for Test/Diagnostic Question should be fully and appropriately completed and the form signed.
Primary Care referrals will be accepted on a standard X-ray request form provided that the same details as required by the orange stripe form are completed. Primary Care are encouraged to use the orange striped form which can be supplied by the Medical Physics Department.
Referral Criteria
Sufficient clinical information must be provided to justify the investigation proceeding.
The clinical indications for a bone scan are continually being extended, but fall into the categories as detailed below.
Investigation | Examples |
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Cause of Bone Pain | • Metastatic tumour • Benign bone tumour • Infection • Fracture • Trauma • Degenerative disease • Peripheral Arthritis • Avascular necrosis • Painful prostheses (but see contraindications) • Osteomalacia • Osteomyelitis • Paget's disease |
Malignancy | • Initial assessment for staging purposes • Assessment of the extent of malignant disease • Assessment of the progression of malignant disease • Assessment of response to treatment or therapy • Investigation of a suspected primary bone tumour (e.g. Ewing's sarcoma, Osteogenic sarcoma, Chondrosarcoma |
Orthopaedic disorders | • Avascular necrosis • Perthes disease • Investigation of painful prostheses |
Benign bone tumours | • Osteoid osteoma • Ivory osteoma • Haemangioma of the spine |
Suspected infection | • Osteomyelitis • Septic arthritis • Infected prosthesis |
Suspected fracture | • Scaphoid • Neck of femur • Fracture from non-accidental injury • Delayed union or non-union of injury |
Suspected exercise-related trauma | • Fracture • Stress fracture • Shin splints |
Known or suspected arthritis | • Osteoarthritis • Synovitis • Rheumatoid arthritis • Reflex Sympathetic Dystrophy Syndrome (Sudeck's) |
Known or suspected metabolic bone disease | • Osteomalacia • Osteoporosis – not for diagnosis (which requires a DEXA scan), but for assessment of complications e.g. fracture, or differentiation from metastatic disease. |
Known or suspected Paget's disease and response to treatment | |
Assessment of the significance of lesions seen on X-ray, CT or MRI |
Contraindications
Medications | Some drugs may interfere with the quality of scintigraphic images: * Aluminium: reduced skeletal tracer uptake, diffuse hepatic tracer uptake, increased renal tracer uptake * Androgen deprivation therapy for prostate cancer (bicalutamide, oestrogens): increased mammary tracer uptake in case of gynecomastia * Bone-modifying agents including bisphosphonates (such as Zolendric Acid) and Denosumab or agents interfering with osteoblast function (e.g. cabozantinib): reduced skeletal tracer uptake * Corticosteroids: reduced skeletal tracer uptake, reduced tracer uptake at fracture sites * Haematopoietic growth factors: increased spinal tracer uptake, possible increased tracer uptake in the appendicular skeleton * Iron: increased renal tracer uptake, increased tracer uptake at site of intramuscular injection, diffuse hepatic tracer uptake * Methotrexate: diffuse hepatic tracer uptake * Nephrotoxic chemotherapy: increased renal tracer uptake and reduced skeletal tracer uptake * Nifedipine: reduced skeletal tracer uptake Please include details on the request of any such medications that the patient is taking. The investigation is best undertaken at a time as long as possible from the last dose i.e. just prior to the next dose to attain the best quality scan. Further information can be found in the The EANM practice guidelines for bone scintigraphy [1]. |
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Surgery | Bone uptake in prostheses can persist for months, even years, as a result of the surgery itself. Post surgery there may be increased bone uptake. Therefore bone scans for investigation of the general causes for painful prosthesis should not be performed within less than 12 months post-surgery. If there is a high suspicion of infection, a White Cell Scan should be considered. |
Medical Conditions | Axial Spondyloarthritis: Bone scintigraphy is not indicated for axial spondyloarthritis [2] Discitis: Bone scans have a sensitivity of 81.4% and specificity of 40.7%. The advantages of this radiopharmaceutical include low cost, low radiation burden, and single-day imaging procedure. It is limited, however, by low specificity. [3] If it is thought that it could be useful for a particular patient, please discuss with the ARSAC licence holder. Myeloma: Do not use isotope bone scans to identify myeloma related bone disease. [4] |
Patient Preparation
Diet | The patient should be well hydrated at the time of administration of the radiopharmaceutical and drink approximately 600ml of fluids between injection and scan. |
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