scholarly journals Long-term treatment of osteoporosis: safety and efficacy appraisal of denosumab

Author(s):  
Athanasios Anastasilakis



2018 ◽  
Vol 178 (3) ◽  
pp. R81-R87 ◽  
Author(s):  
Robert A Adler

Modern osteoporosis treatment began in the mid-1990s with the approval of amino-bisphosphonates, anti-resorptive agents that have been shown to decrease osteoporotic fracture risk by about half. In 2005, the first cases of atypical femoral fractures (AFF), occurring in the shaft of the femur, were reported. Since then, more cases have been found, leading to great concern among patients and a dramatic decrease in bisphosphonate prescribing. The pathogenesis and incidence of AFF are reviewed herein. Management and an approach to prevention or early detection of AFF are also provided. Denosumab, a more recently approved anti-resorptive medication has also been associated with AFF. Long-term management of osteoporosis and prevention of fracture are challenging in light of this serious but uncommon side effect, yet with an aging population osteoporotic fracture is destined to increase in frequency.



2008 ◽  
Vol 20 (3) ◽  
pp. 399-401 ◽  
Author(s):  
L. Spicuzza ◽  
C. Sciuto ◽  
M. La Rosa


1994 ◽  
Vol 17 ◽  
pp. S74-S87 ◽  
Author(s):  
E. Moll ◽  
N. Neumann ◽  
W. Schmid-Burgk ◽  
M. Stabl ◽  
R. Amrein




2014 ◽  
Vol 68 (7) ◽  
pp. 498-505 ◽  
Author(s):  
Hideaki Katagiri ◽  
Mauricio Tohen ◽  
David P. McDonnell ◽  
Shinji Fujikoshi ◽  
Michael Case ◽  
...  


1996 ◽  
Vol 24 (3) ◽  
pp. 311-315 ◽  
Author(s):  
E Pogliani ◽  
M Milani

Patients with chronic myeloproliferative disease are at increased risk of both thromboembolic and haemorrhagic complications. Cerebral thrombosis is a common cause of death in myeloproliferative disease patients. Picotamide is a new anti-platelet drug sharing a dual anti-thromboxane activity: inhibition of thromboxane A2 synthase and thromboxane A2 receptor antagonism. Picotamide inhibits in vitro and ex vivo platelet aggregation induced by different agonists. Interestingly, in vitro studies show that picotamide is able to increase prostacycline biosynthesis. In the clinical setting, picotamide treatment induces only a slight prolongation of bleeding time. The safety and efficacy of picotamide long-term treatment in 15 patients with essential thrombocytosis and a positive history of previous thromboembolic events was evaluated. After 12-month treatment with picotamide no patients suffered from thrombotic events and only one minor and transient bleeding episode was observed. This observational long-term trial shows that picotamide treatment in patients with thrombocytosis at high risk of thrombotic events is safe and well tolerated. Picotamide did not increase the risk of bleeding in these patients, while at the same time, no thrombotic events were observed during the 1-year treatment.



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