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Effect of Teriparatide or Risedronate in Elderly Patients With a Recent Pertrochanteric Hip Fracture: Final Results of a 78-Week Randomized Clinical Trial

Malouf-Sierra, Jorge (author)
Hospital San Pablo, Spain
Tarantino, Umberto (author)
University of Tor Vergata, Italy
Garcia-Hernandez, Pedro A. (author)
University Hospital, Mexico
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Corradini, Costantino (author)
University of Milan, Italy
Overgaard, Soren (author)
University of Southern Denmark, Denmark
Stepan, Jan J. (author)
Charles University of Prague, Czech Republic; Charles University of Prague, Czech Republic
Borris, Lars (author)
Aarhus University Hospital, Denmark
Lespessailles, Eric (author)
CHR Orleans, France; Orleans University, France
Frihagen, Frede (author)
Oslo University Hospital, Norway
Papavasiliou, Kyriakos (author)
Aristotle University of Thessaloniki, Greece
Petto, Helmut (author)
Eli Lilly, Austria
Aspenberg, Per (author)
Linköpings universitet,Avdelningen för Kirurgi, Ortopedi och Onkologi,Medicinska fakulteten,Region Östergötland, Ortopedkliniken i Linköping
Ramon Caeiro, Jose (author)
University of Santiago de Compostela, Spain
Marin, Fernando (author)
Eli Lilly Research Centre Ltd, England
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 (creator_code:org_t)
2017-01-26
2017
English.
In: Journal of Bone and Mineral Research. - : WILEY. - 0884-0431 .- 1523-4681. ; 32:5, s. 1040-1051
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • We present final results of a study comparing teriparatide 20g every day (QD) with risedronate 35mg once per week (QW) started within 2 weeks after surgery for a pertrochanteric hip fracture. Patients with BMD T-score-2.0 and 25OHD 9.2ng/mL were randomized to receive 26-week double-dummy treatment plus calcium and vitamin D, followed by 52-week open-label treatment with the same assigned active drug. Primary endpoint was change from baseline in lumbar spine (LS) BMD at 78 weeks. Secondary and exploratory endpoints were change in BMD at the proximal femur, function, hip pain (Charnley score and 100mm Visual Analog Scale [VAS]), quality of life (Short Form-36), radiology outcomes, and safety. Data were analyzed with mixed models for repeated measures (MMRM) and logistic regression. Totally, 224 patients were randomized; 171 (teriparatide: 86) contributed to the efficacy analyses (mean +/- SD age: 77 +/- 7.7 years, 77% females). Mean baseline LS, femoral neck (FN), and total hip (TH) T-scores were -2.16, -2.63, and -2.51, respectively. At 78 weeks, BMD increased significantly more with teriparatide compared to risedronate at the LS (+11.08% versus +6.45%; pamp;lt;0.001) and FN (+1.96% versus -1.19%; p=0.003), with no significant between-group difference in TH BMD. Timed up-and-go (TUG) test was significantly faster with teriparatide at 6, 12, 18, and 26 weeks (differences: -3.2 to -5.9s; p=0.045 for overall difference). Hip pain during TUG test by 100mm VAS was significantly lower with teriparatide at 18 weeks (adjusted difference: -11.3mm, p=0.033; -10.0 and -9.3mm at 12 and 26 weeks, respectively; p=0.079 for overall difference). Other secondary and exploratory outcomes were not different. Teriparatide group showed two new hip fractures versus seven with risedronate (p=0.171) and more frequent hypercalcemia and hyperuricemia. In conclusion, 78-week treatment with teriparatide showed significantly greater increases in LS and FN BMD, less pain, and a faster TUG test versus risedronate. (c) 2016 American Society for Bone and Mineral Research.

Subject headings

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

Keyword

TERIPARATIDE; BONE MINERAL DENSITY; PERTROCHANTERIC HIP FRACTURE; FRACTURE RECOVERY; BISPHOSPHONATES

Publication and Content Type

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art (subject category)

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