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Effects of Teriparatide Compared with Risedronate on Recovery After Pertrochanteric Hip Fracture Results of a Randomized, Active-Controlled, Double-Blind Clinical Trial at 26 Weeks

Aspenberg, Per (författare)
Linköpings universitet,Avdelningen för kliniska vetenskaper,Medicinska fakulteten,Region Östergötland, Ortopedkliniken i Linköping
Malouf, Jorge (författare)
Hospital San Pablo, Spain
Tarantino, Umberto (författare)
University of Roma Tor Vergata, Italy
visa fler...
Garcia-Hernandez, Pedro A. (författare)
University Hospital, Mexico
Corradini, Costantino (författare)
University of Milan, Italy
Overgaard, Soren (författare)
Odense University Hospital, Denmark; University of Southern Denmark, Denmark
Stepan, Jan J. (författare)
Charles University of Prague, Czech Republic; Charles University of Prague, Czech Republic
Borris, Lars (författare)
University Hospital, Denmark
Lespessailles, Eric (författare)
CHR Orleans, France; University of Orleans, France
Frihagen, Frede (författare)
Oslo University Hospital, Norway
Papavasiliou, Kyriakos (författare)
Aristotle University of Thessaloniki, Greece
Petto, Helmut (författare)
Eli Lilly, Austria
Ramon Caeiro, Jose (författare)
University of Santiago de Compostela, Spain
Marin, Fernando (författare)
Eli Lilly Research Centre, England
visa färre...
 (creator_code:org_t)
JOURNAL BONE JOINT SURGERY, 2016
2016
Engelska.
Ingår i: Journal of Bone and Joint Surgery. American volume. - : JOURNAL BONE JOINT SURGERY. - 0021-9355 .- 1535-1386. ; 98:22
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Osteoporosis drugs might affect fracture-healing. We therefore studied the effects of teriparatide in comparison with risedronate on recovery after pertrochanteric hip fractures. Methods: The study was a randomized, multicenter, active-controlled, 78-week trial comparing teriparatide (20 mg/day) with risedronate (35 mg/week) initiated within 2 weeks after fixation of a low-trauma pertrochanteric hip fracture (AO/OTA 31-A1 or 31-A2). The main inclusion criteria were a bone mineral density T-score of amp;lt;=-22.0 and 25-OH-vitamin D of amp;gt;= 9.2 ng/mL. During the first 26 weeks, patients received study medication with oral or injectable placebo plus calcium and vitamin D in a double-blinded fashion. Secondary (Timed Up-and-Go [TUG] test, hip pain, Short Form [SF]-36 health status, and safety) and exploratory (radiographic outcomes and ability to walk) 26-week end points are reported. Results: Of the 224 patients who were randomized, 171 (86 teriparatide, 85 risedronate) were included in the analysis. The mean age was 77 +/- 8 years, 77% were female, and 26% had a prior history of low-trauma fracture. The teriparatide group completed the TUG test in a shorter time at 6, 12, 18, and 26 weeks (differences of 25.7, -4.4, -3.1, and -3.1 seconds, respectively; p = 0.021 for the overall difference). They also reported less pain on a visual analog scale immediately after the TUG test at 12 and 18 weeks (adjusted absolute differences of 10.6 and 11.9 mm, respectively; p amp;lt; 0.05). There were no significant between-group differences in the SF-36 score, Charnley hip pain score, ability to walk, or use of walking aids during follow-up. Radiographic healing at 6, 12, and 26 weeks, mechanical failure of the implant (teriparatide, 7; risedronate, 8), loss of reduction (teriparatide, 2; risedronate, 4), and nonunion (0 cases) were not significantly different. Mild hypercalcemia and hyperuricemia were more frequent with teriparatide. Conclusions: Teriparatide was associated with less pain and a shorter time to complete the TUG test between 6 and 26 weeks compared with risedronate. Other fracture-recovery outcomes were similar. The results should be interpreted with caution as these were secondary end points.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Ortopedi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Orthopaedics (hsv//eng)

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