Fracture strength of the proximal femur injected with a calcium sulfate/hydroxyapatite bone substitute.


Journal

Clinical biomechanics (Bristol, Avon)
ISSN: 1879-1271
Titre abrégé: Clin Biomech (Bristol, Avon)
Pays: England
ID NLM: 8611877

Informations de publication

Date de publication:
03 2019
Historique:
received: 10 01 2019
revised: 05 03 2019
accepted: 11 03 2019
pubmed: 25 3 2019
medline: 24 3 2020
entrez: 24 3 2019
Statut: ppublish

Résumé

Available interventions for preventing fragility hip fractures show limited efficacy. Injection of a biomaterial as bone substitute could increase the fracture strength of the hip. This study aimed to show the feasibility of injecting a calcium sulfate/hydroxyapatite based biomaterial in the femoral neck and to calculate the consequent change in strength using the finite element method. Five patients were injected with 10 ml calcium sulfate/hydroxyapatite in their femoral neck. Quantitative CT scans were taken before and after injection. Five additional patients with fragility hip fractures were also scanned and the images from the non-fractured contralateral sides were used. Finite element models were created for all proximal femora with and without injection and the models were tested under stance and sideways fall loading until fracture. The change in fracture strength caused by the injection was calculated. Additionally, perturbations in volume, location, and stiffness of the injected material were created to investigate their contribution to the fracture strength increase. The 10 ml injection succeeded in all patients. Baseline simulations showed theoretical fracture strength increases of 0-9%. Volume increase, change in location and increase in stiffness of the material led to increases in fracture strength of 1-27%, -8-26% and 0-17%, respectively. Altering the location of the injection to a more lateral position and increasing the stiffness of the material led to increases in fracture strength of up to 42%. This study shows that an injection of calcium sulfate/hydroxyapatite is feasible and can theoretically increase the hip's fracture strength.

Sections du résumé

BACKGROUND
Available interventions for preventing fragility hip fractures show limited efficacy. Injection of a biomaterial as bone substitute could increase the fracture strength of the hip. This study aimed to show the feasibility of injecting a calcium sulfate/hydroxyapatite based biomaterial in the femoral neck and to calculate the consequent change in strength using the finite element method.
METHODS
Five patients were injected with 10 ml calcium sulfate/hydroxyapatite in their femoral neck. Quantitative CT scans were taken before and after injection. Five additional patients with fragility hip fractures were also scanned and the images from the non-fractured contralateral sides were used. Finite element models were created for all proximal femora with and without injection and the models were tested under stance and sideways fall loading until fracture. The change in fracture strength caused by the injection was calculated. Additionally, perturbations in volume, location, and stiffness of the injected material were created to investigate their contribution to the fracture strength increase.
FINDINGS
The 10 ml injection succeeded in all patients. Baseline simulations showed theoretical fracture strength increases of 0-9%. Volume increase, change in location and increase in stiffness of the material led to increases in fracture strength of 1-27%, -8-26% and 0-17%, respectively. Altering the location of the injection to a more lateral position and increasing the stiffness of the material led to increases in fracture strength of up to 42%.
INTERPRETATION
This study shows that an injection of calcium sulfate/hydroxyapatite is feasible and can theoretically increase the hip's fracture strength.

Identifiants

pubmed: 30903873
pii: S0268-0033(19)30023-3
doi: 10.1016/j.clinbiomech.2019.03.008
pii:
doi:

Substances chimiques

Biocompatible Materials 0
Bone Substitutes 0
Durapatite 91D9GV0Z28
Calcium Sulfate WAT0DDB505

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

172-178

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Joeri Kok (J)

Department of Biomedical Engineering, Lund University, Box 118, 221 00 Lund, Sweden. Electronic address: joeri.kok@bme.lth.se.

Aurimas Širka (A)

Department of Orthopedics and Traumatology, Lithuanian University of Health Sciences, A. Mickevičiaus g. 9, LT 44307 Kaunas, Lithuania.

Lorenzo Grassi (L)

Department of Biomedical Engineering, Lund University, Box 118, 221 00 Lund, Sweden. Electronic address: lorenzo.grassi@bme.lth.se.

Deepak Bushan Raina (DB)

Department of Orthopedics, Clinical Sciences, Lund University, Box 118, 221 00 Lund, Sweden. Electronic address: deepak.raina@med.lu.se.

Šarūnas Tarasevičius (Š)

Department of Orthopedics and Traumatology, Lithuanian University of Health Sciences, A. Mickevičiaus g. 9, LT 44307 Kaunas, Lithuania.

Magnus Tägil (M)

Department of Orthopedics, Clinical Sciences, Lund University, Box 118, 221 00 Lund, Sweden. Electronic address: magnus.tagil@med.lu.se.

Lars Lidgren (L)

Department of Orthopedics, Clinical Sciences, Lund University, Box 118, 221 00 Lund, Sweden.

Hanna Isaksson (H)

Department of Biomedical Engineering, Lund University, Box 118, 221 00 Lund, Sweden; Department of Orthopedics, Clinical Sciences, Lund University, Box 118, 221 00 Lund, Sweden. Electronic address: hanna.isaksson@bme.lth.se.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH