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Impact of osteoporosis and osteoporosis medications on fracture healing: a narrative review.
Chandran, M; Akesson, K E; Javaid, M K; Harvey, N; Blank, R D; Brandi, M L; Chevalley, T; Cinelli, P; Cooper, C; Lems, W; Lyritis, G P; Makras, P; Paccou, J; Pierroz, D D; Sosa, M; Thomas, T; Silverman, S.
Affiliation
  • Chandran M; Osteoporosis and Bone Metabolism Unit, Department of Endocrinology, Singapore General Hospital, DUKE NUS Medical School, Singapore, Singapore. mchandran7@gmail.com.
  • Akesson KE; Clinical and Molecular Osteoporosis Research Unit, Department of Clinical Sciences, Lund University, Department of Orthopedics, Skåne University Hospital, Malmö, Sweden.
  • Javaid MK; NIHR Musculoskeletal Biomedical Research Unit, University of Oxford, Oxford, UK.
  • Harvey N; MRC Lifecourse Epidemiology Centre, University of Southampton, NIHR Southampton Biomedical Research Centre, University of Southampton, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • Blank RD; Garvan Institute of Medical Research, Medical College of Wisconsin, Darlinghurst, NSW, Australia.
  • Brandi ML; Medical College of Wisconsin, Milwaukee, WI, USA.
  • Chevalley T; Department of Biomedical, Experimental and Clinical Sciences, University of Florence, Largo Palagi 1, Florence, Italy.
  • Cinelli P; Division of Bone Diseases, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.
  • Cooper C; Department of Trauma Surgery, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
  • Lems W; MRC Lifecourse Epidemiology Centre, University of Southampton, NIHR Southampton Biomedical Research Centre, University of Southampton, University Hospitals Southampton NHS Foundation Trust, Southampton, UK.
  • Lyritis GP; NIHR Oxford Biomedical Research Unit, University of Oxford, Oxford, UK.
  • Makras P; Department of Rheumatology, Amsterdam UMC, Location VUmc, Amsterdam, The Netherlands.
  • Paccou J; Hellenic Osteoporosis Foundation, Athens, Greece.
  • Pierroz DD; Department of Medical Research, 251 Hellenic Air Force & VA General Hospital, Athens, Greece.
  • Sosa M; Department of Rheumatology, MABlab ULR 4490, CHU Lille, Univ. Lille, 59000, Lille, France.
  • Thomas T; International Osteoporosis Foundation, Nyon, Switzerland.
  • Silverman S; University of Las Palmas de Gran Canaria, Investigation Group on Osteoporosis and Mineral Metabolism, Canary Islands, Spain.
Osteoporos Int ; 35(8): 1337-1358, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38587674
ABSTRACT
Antiresorptive medications do not negatively affect fracture healing in humans. Teriparatide may decrease time to fracture healing. Romosozumab has not shown a beneficial effect on human fracture healing.

BACKGROUND:

Fracture healing is a complex process. Uncertainty exists over the influence of osteoporosis and the medications used to treat it on fracture healing.

METHODS:

Narrative review authored by the members of the Fracture Working Group of the Committee of Scientific Advisors of the International Osteoporosis Foundation (IOF), on behalf of the IOF and the Société Internationale de Chirurgie Orthopédique et de Traumatologie (SICOT).

RESULTS:

Fracture healing is a multistep process. Most fractures heal through a combination of intramembranous and endochondral ossification. Radiographic imaging is important for evaluating fracture healing and for detecting delayed or non-union. The presence of callus formation, bridging trabeculae, and a decrease in the size of the fracture line over time are indicative of healing. Imaging must be combined with clinical parameters and patient-reported outcomes. Animal data support a negative effect of osteoporosis on fracture healing; however, clinical data do not appear to corroborate with this. Evidence does not support a delay in the initiation of antiresorptive therapy following acute fragility fractures. There is no reason for suspension of osteoporosis medication at the time of fracture if the person is already on treatment. Teriparatide treatment may shorten fracture healing time at certain sites such as distal radius; however, it does not prevent non-union or influence union rate. The positive effect on fracture healing that romosozumab has demonstrated in animals has not been observed in humans.

CONCLUSION:

Overall, there appears to be no deleterious effect of osteoporosis medications on fracture healing. The benefit of treating osteoporosis and the urgent necessity to mitigate imminent refracture risk after a fracture should be given prime consideration. It is imperative that new radiological and biological markers of fracture healing be identified. It is also important to synthesize clinical and basic science methodologies to assess fracture healing, so that a convergence of the two frameworks can be achieved.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteoporosis / Fracture Healing / Bone Density Conservation Agents / Osteoporotic Fractures Limits: Animals / Humans Language: En Journal: Osteoporos Int Journal subject: METABOLISMO / ORTOPEDIA Year: 2024 Type: Article Affiliation country: Singapore

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteoporosis / Fracture Healing / Bone Density Conservation Agents / Osteoporotic Fractures Limits: Animals / Humans Language: En Journal: Osteoporos Int Journal subject: METABOLISMO / ORTOPEDIA Year: 2024 Type: Article Affiliation country: Singapore