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ill-fitting dentures. She had been edentulous for over 50 years. Her medical history
was significant for osteoporosis, hypothyroidism, nephrolithiasis, thyroidectomy,
cholecystectomy, hysterectomy, an ankle fracture suffered in 1986, and a hip
fracture sustained in 1987 that ultimately resulted in total hip replacement. The
patient was taking thyroid and estrogen replacement, as well as calcium and vitamin
D supplements. Clinical examination revealed severe atrophy of the maxilla and
mandible with virtually no residual alveolar ridges (Fig 1). After she had been
evaluated by her internist and no contraindications for surgery were reported, the
patient underwent placement of five endosseous implants in the anterior mandible
and augmentation of the maxillary residual alveolar ridge with nonresorbable
particulate hydroxyapatite. The date of the original surgery was August 31, 1989.
The surgical sites healed without complication, and the implants were uncovered on
December 6, 1989. The patient was restored with a new complete maxillary denture
and fixed hybrid mandibular prosthesis on January 3, 1990.
The patient returned for five routine recall appointments between May 1990 and
June 1991. Panoramic radiographs taken at these appointments revealed normal
healing (Fig 2). However, approximately 9 months following radiographic
examination, the patient returned complaining of pain in the mandible. A new
panoramic radiograph revealed extensive osteolysis around all five implants (Fig 3).
On questioning, the patient related that she had been placed on etidronate disodium
(Didronel, Norwich Eaton Pharmaceuticals, Norwich, New York) in December of
1991 to “build up her bones.” In addition, the patient had recently started a liquid
diet for weight loss that resulted in loosening of her maxillary denture, which caused
her to clench her teeth in an attempt to retain the denture. Importantly, the
radiographic appearance of uniform radiolucencies around each implant was unlike
anything previously observed or reported in the literature. After consultation with
the patient’s internist, the Didronel was discontinued and she was instructed not to
wear her denture. Unfortunately, the osteolysis resulted in loss of all five implants,
which were removed on April 30th, 1992 (Fig 4).
Discussion
Etidronate disodium (1-hydroxyethylidene or EHDP) is a diphosphonate that affects
bone metabolism. It has been used in the United States for the management of
Paget’s disease, osteoporosis, hypercalcemia of malignancy, and for the treatment of
heterotopic ossification following total hip replacement and spinal trauma. It may be
administered orally or intravenously. Low dose therapy ranges from 2.5 to 10
mg/kg/day, while higher dosage regimens of up to 20 mg/kg/day are reserved for
patients who fail to respond to low-dosage regimens. Didronel-induced osteomalacia
from continuous use in patients with osteoporosis has led to the development of
cyclic therapy regimens; the usual regimen consists of 2 weeks of therapy followed
by 10 to 13 weeks without medication.
Didronel has been demonstrated to arrest bone activation and/or turnover
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