Description

A 69-year-old man presented with deformities to his mid-thighs bilaterally and inability to weight-bear. He had fallen from standing height after tripping over a loose rug at his home. He suffered no other injuries and examination indicated no neurovascular deficits. Prior to injury, he had been independently mobile and fully weight-bearing without issue. Plain radiographs indicated bilateral femoral shaft fractures (figures 1 and 2). There was no clinical or radiographical evidence of pelvic or proximal femoral fractures. His medical history included osteoporosis, coronary angioplasty and hypertension. His current medication included: risedronate (11 years’ use), ramipril, atorvastatin and aspirin. He underwent bilateral fascia iliaca compartment blocks with subsequent intramedullary fracture fixation.

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Figure 1

Anteroposterior and lateral plain film radiographs of right femur fracture.

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Figure 2

Anteroposterior and lateral plain film radiographs of left femur fracture.

Bisphosphonates (such as risedronate) are a class of drug widely used in the treatment of osteoporosis. They decrease the rate of bone mineral density (BMD) loss by inhibiting osteoclastic bone resorption, the process through which essential minerals such as calcium are reabsorbed from bone.1 2 Adverse effects of bisphosphonate use include musculoskeletal pain, hypocalcaemia, oesophageal irritation, atrial fibrillation and jaw osteonecrosis.2

Atypical subtrochanteric femoral insufficiency fractures are an extremely rare adverse effect of long-term bisphosphonate use. They have an estimated incidence of 1 in 1000 per year; however, the evidence suggesting a definitive link is still somewhat controversial.3–5 Such fractures may be atraumatic or caused by low-energy impact and are often bilateral.3 6 7 Affected patients have usually been on >3–5 years of bisphosphonate therapy and may report acute-to-chronic histories of thigh or groin pain.3 4 8 Intramedullary nailing is the recommended mode of treatment.9

The mechanism through which bisphosphonates may contribute to atypical fracture patterns, such as in this patient, is yet to be definitively determined. The proposed mechanism is decreased osteoclastic activity and impeded bony remodelling following prolonged bisphosphonate use, which contributes to increased skeletal fragility due to the accumulation of bony microdamages which would otherwise normally be repaired in individuals not on bisphosphonates.4 6 10

Although the optimal duration of bisphosphonate therapy remains unclear, recent recommendations suggest a 3–5 year therapy duration (5 years for risedronate) for patients at ‘low-risk’ of fracture, at which time a ‘drug holiday’' and reassessment of BMD should be undertaken.11 12

This case adds to the still controversial evidence that bisphosphonates may be linked with atypical femoral fractures. Further research is needed to infer a definitive link. This patient recovered well from his surgery and was discharged 4 weeks later after a period of rehabilitation. On clinical recommendation, he agreed to stop taking risedronate and will undergo BMD reassessment with subsequent discussions concerning further osteoporosis management.

Bisphosphonates are still a very welcome revolutionary drug class for the treatment of osteoporosis. The overall risk of both typical and atypical femoral fractures still remains significantly lower in patients taking bisphosphonates.3 However it would be advisable for medical practitioners to engage in regular reviews of long-term medication, patient counselling regarding this rare potential adverse effect and BMD reassessment after 3–5 years of bisphosphonate therapy with consideration of ‘drug holidays’.