Conditions
Extracting in a patient on antiresorptives
What medication-related osteonecrosis of the jaw actually tracks, why the osteoporosis and oncology figures cannot be compared without their denominators, what drug holidays and CTX testing have and have not shown, and how I decide who to treat and who to refer.
The risk of osteonecrosis of the jaw after an extraction in a patient on an antiresorptive is set mostly by how much of the drug the patient has received, and the gap between the two populations is large: an international consensus put the incidence at 1% to 15% in oncology patients and 0.001% to 0.01% in osteoporosis, and a survey-and-examination study of patients on oral bisphosphonates found 0.10%, so the figure that gets quoted depends heavily on the denominator and the method behind it. In cancer patients the risk rose with the number of infusions and the duration of treatment in cohort studies, and in three pooled phase III trials it was 1.3% with zoledronic acid and 1.8% with denosumab, a difference that was not significant there, although a later meta-analysis of 23 trials did find a higher incidence with denosumab. Denosumab differs from the bisphosphonates in that its effect wears off rather than residing in bone, and stopping it produces a rebound in bone turnover with multiple vertebral fractures in some patients, which makes an unplanned pause a medical decision rather than a dental one. Short drug holidays before extraction have not been shown to reduce the risk in the retrospective cohorts and meta-analyses that have tested them, in oncology and osteoporosis patients, though one large-animal study found a benefit, and serum CTX has performed poorly as a predictor in three systematic reviews. My own position is that the risk follows cumulative dose — duration times the amount given — rather than the timing within an infusion cycle; I refer patients above my comfort level so that post-operative complications are managed by someone equipped for them, I do not use CTX, and I usually give antibiotics after the extraction, though there is a fair argument for starting them before.
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This piece is education for clinicians, not advice for any patient. It describes conditions, precautions and the reasoning behind decisions at the level of the condition; it does not give step-by-step operative technique, and it is not a substitute for the judgement of the treating clinician, the patient's physicians, or the guidance of the relevant professional bodies. Reading it creates no clinician–patient or consulting relationship, and nothing here is direction to any reader about a patient in front of them.
Drug doses, maximums and formulations change and differ between references and package inserts — verify every figure against a current primary source before you rely on it. Where a position here differs from current product labelling that is stated in the text, and the labelling, not this page, is the reference. Guidance cited is drawn from several countries and professional bodies; which applies to you is a question for your own regulator and permit. Passages describing occupational exposure, equipment or staffing are general background rather than an occupational-health assessment of any workplace.