TY - JOUR
T1 - Republished
T2 - Severe hypophosphataemia following oral bisphosphonate treatment in a patient with osteoporosis
AU - Bagger, Louise Wulff
AU - Hansen, Per Kim Dyhr
AU - Schwarz, Peter
AU - Nielsen, Barbara Rubek
N1 - Publisher Copyright:
© 2021 Lippincott Williams and Wilkins. All rights reserved.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/7
Y1 - 2021/7
N2 - A 76-year- old woman was treated with oral bisphosphonate, alendronate, for osteoporosis in an outpatient clinic. Routine blood tests 4 months after alendronate prescription surprisingly revealed severe hypophosphataemia. The patient was hospitalised and treated with intravenous and oral phosphate supplements. Alendronate was later reintroduced as treatment for osteoporosis and the patient once again presented with severe hypophosphataemia in subsequent routine blood tests. The patient had only presented with lower extremity pain, muscle weakness and difficulty walking. Blood tests in the emergency department both times reconfirmed severe hypophosphataemia. Plasma (p-) ionised calcium levels were normal or slightly elevated and p-parathyroid hormone levels were normal or slightly suppressed. The p-25-hydroxyvitamin- D and p-creatine were in the normal range. Critical illness, malabsorption, nutritional issues and genetics were reviewed as potential causes but considered unlikely. Phosphate levels were quickly restored each time on replacement therapy and the case was interpreted as bisphosphonate-induced severe hypophosphataemia.
AB - A 76-year- old woman was treated with oral bisphosphonate, alendronate, for osteoporosis in an outpatient clinic. Routine blood tests 4 months after alendronate prescription surprisingly revealed severe hypophosphataemia. The patient was hospitalised and treated with intravenous and oral phosphate supplements. Alendronate was later reintroduced as treatment for osteoporosis and the patient once again presented with severe hypophosphataemia in subsequent routine blood tests. The patient had only presented with lower extremity pain, muscle weakness and difficulty walking. Blood tests in the emergency department both times reconfirmed severe hypophosphataemia. Plasma (p-) ionised calcium levels were normal or slightly elevated and p-parathyroid hormone levels were normal or slightly suppressed. The p-25-hydroxyvitamin- D and p-creatine were in the normal range. Critical illness, malabsorption, nutritional issues and genetics were reviewed as potential causes but considered unlikely. Phosphate levels were quickly restored each time on replacement therapy and the case was interpreted as bisphosphonate-induced severe hypophosphataemia.
KW - calcium and bone
KW - drugs: endocrine system
KW - geriatric medicine
KW - unwanted effects / adverse reactions
UR - http://www.scopus.com/inward/record.url?scp=85106865372&partnerID=8YFLogxK
U2 - 10.1136/dtb.2021.235083rep
DO - 10.1136/dtb.2021.235083rep
M3 - Journal article
C2 - 34031179
SN - 0012-6543
VL - 59
SP - 107
EP - 111
JO - Drug and therapeutics bulletin
JF - Drug and therapeutics bulletin
IS - 7
M1 - 235083rep
ER -