| المساهمون: |
Nash, Peter, Hall, Stephen, Jones, Graeme, Goemaere, Stefan, Kaufman, Jean-Marc, Raeman, Frank, Hala, Tomas, Kasalicky, Petr, Palicka, Vladimir, Valter, Ivo, Pail, Margus, Maasalu, Katre, Heikkinen, Jorma, Audran, Maurice, Le Jeunne, Claire, Schaeverbeke, Thierry, Li, Edmund, Zeher, Margit, Horváth, Katalin, Vered, Iris, Tordjman, Karen M, Eshed, Varda, Benbasat, Carlos, Ish-Shalom, Sophia, Alekna, Vidmantas, Baranauskaitė, Asta, Tamulaitienė, Marija, Venalis, Algirdas, Sawicki, Andrzej, Przedlacki, Jerzy, Lipinski, Krzysztof, Korkosz, Mariusz, Czerwinski, Edward, Codreanu, Catalin, Sarbu, Adrian, Zbranca, Eusebie, Bolosiu, Horatiu, Blanco, Francisco Javier, Mellibovsky, Leonardo, Lippuner, Kurt, Theiler, Robert, Rizzoli, René, Cooper, Cyrus, Eastell, Richard, Keen, Richard, Recknor, Christopher, Emkey, Ronald, Gallagher, Francis J, Adler, Robert, Malamet, Raymond, Klein, Steven, Jackson, Rebecca |
| الوصف: |
Background. Persistent use of glucocorticoid drugs is associated with bone loss and increased fracture risk. Concurrent oral bisphosphonates increase bone mineral density and reduce frequency of vertebral fractures, but are associated with poor compliance and adherence. We aimed to assess whether one intravenous infusion of zoledronic acid was non-inferior to daily oral risedronate for prevention and treatment of glucocorticoid-induced osteoporosis. Methods. This 1-year randomised, double-blind, double-dummy, non-inferiority study of 54 centres in 12 European countries, Australia, Hong Kong, Israel, and the USA, tested the effectiveness of 5 mg intravenous infusion of zoledronic acid versus 5 mg oral risedronate for prevention and treatment of glucocorticoid-induced osteoporosis. 833 patients were randomised 1:1 to receive zoledronic acid (n=416) or risedronate (n=417). Patients were stratified by sex, and allocated to prevention or treatment subgroups dependent on duration of glucocorticoid use immediately preceding the study. The treatment subgroup consisted of those treated for more than 3 months (272 patients on zoledronic acid and 273 on risedronate), and the prevention subgroup of those treated for less than 3 months (144 patients on each drug). 62 patients did not complete the study because of adverse events, withdrawal of consent, loss to follow-up, death, misrandomisation, or protocol deviation. The primary endpoint was percentage change from baseline in lumbar spine bone mineral density. Drug efficacy was assessed on a modified intention-to-treat basis and safety was assessed on an intention-to-treat basis. This trial is registered with ClinicalTrials.gov, number NCT00100620. [.]. |
