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Orthopaedic Proceedings
Vol. 105-B, Issue SUPP_2 | Pages 101 - 101
10 Feb 2023
Tan W Yu S Gill T Campbell D Umapathysivam K Smitham P
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The progressive painful and disabling predicament of patients with severe osteoarthritis awaiting a total hip or knee arthroplasty (THA/TKA) results in a decline in muscle mass, strength and function also known as Sarcopenia.

We conducted a cross-sectional, prospective study of patients on the waiting-list for a THA/TKA in the South Australian public healthcare system and compared the findings to healthy participants and patients newly referred from their general practitioners. Participants with a history of joint replacements, pacemakers and cancers were excluded from this study. Outcomes of this study included (i) sarcopenia screening (SARC-F ≥4); (ii) sarcopenia, defined as low muscle strength (hand grip strength M<27kg; F<16kg), low muscle quality (skeletal muscle index M<27%, F<22.1%) and low physical performance (short physical performance battery ≤8). Additional outcomes include descriptions of the recruitment feasibility, randomisation and suitability of the assessment tools.

29 healthy controls were recruited; following screening, 83% (24/29) met the inclusion criteria and 75% (18/24) were assessed. 42 newly referred patients were recruited; following screening, 67% (30/45) met the inclusion criteria and 63% (19/30) were assessed. 68 waiting list patients were recruited; following recruitment, 24% (16/68) met the inclusion criteria and 75% (12/16) were assessed. Preliminary data shows increasing waiting time is associated with higher SARC-F scores, lower hand grip strength and lower muscle quality.

As a pilot study, preliminary data demonstrate that: (1) study subjects’ willingness to participate will enable a larger study to be conducted to establish the prevalence of sarcopenia and the diagnostic cut-off points for this patient group. (2) SARC-F is a suitable tool to screen for sarcopenia. (3) There is a positive correlation between waiting time for a THA/TKA and sarcopenia.


Orthopaedic Proceedings
Vol. 95-B, Issue SUPP_34 | Pages 287 - 287
1 Dec 2013
Puthumanapully PK Shearwood-Porter N Stewart M Kowalski R Browne M Dickinson A
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Introduction. Implant-cement debonding at the knee has been reported previously [1]. The strength of the mechanical interlock of bone cement on to an implant surface can be associated with both bone cement and implant related factors. In addition to implant surface profile, sub-optimal mixing temperatures and waiting times prior to cement application may weaken the strength of the interlock. Aims. The study aimed to investigate the influence of bone cement related factors such as mixing temperature, viscosity, and the mixing and waiting times prior to application, in combination with implant surface roughness, on the tensile strength at the interface. Materials and Methods. Tensile tests were carried out on two types of hand-mixed cement, high (HV) and medium viscosity (MV), sandwiched between two cylindrical Cobalt-Chrome coupons with either smooth (60 grit) or rough (20 grit) surface finishes. 144 Specimens were prepared with a cement thickness layer of 2.5 mm in customised rigs (Figure 1). The samples were grouped and tested at two mixing temperatures (23 and 19 degrees), at different mixing times (HV-30s, MV-45s). Waiting times after mixing were varied between early (1.5 min), optimal (4.5 min) or late (8 min); for HV and 4 min, 7.5 min and 11 min for MV cements. All the samples were cured for 24 hours prior to testing. The peak force and stress was calculated for all specimens. Results and Conclusion. Surface Finish: Rough surfaced samples had significantly higher (p < 0.05) mean tensile forces and stress than smooth samples at both 19 and 23 degrees across HV and MV cement types. Cement Type: MV cements, when applied to rough samples with waiting times of 4 minutes at 23 degrees, and 11 minutes at 19 degrees, resulted in the highest peak tensile forces, followed by 7.5 minutes at 23 and 19 degrees respectively (Figure 2). Temperature at different application times for rough and smooth samples: for MV cement, rough samples prepared at 23 degrees, 4 minutes, and smooth samples at 19 degrees, 7.5 minutes were found to be significantly better (p < 0.05) than their counterparts. For HV cement, 23 degrees was found to be better (p < 0.05) for smooth samples at applications times of 4.5 and 8 minutes and 19 degrees for application times of 1.5 minutes. No significant difference was noted for rough samples for the same. Application times at different temperatures for rough and smooth samples: at both 19 and 23 degrees, there were no differences between application times within the rough sample groups for HV or MV. However, for smooth samples, HV cement, tensile forces were significantly higher (p < 0.05) at 23 degrees in the following order; 8 minutes > 4.5 minutes > 1.5. The results show that implant surface roughness and cement mixing time, temperature, viscosity and application times affect the strength of the interlock at the interface


Bone & Joint Open
Vol. 5, Issue 11 | Pages 953 - 961
1 Nov 2024
Mew LE Heaslip V Immins T Ramasamy A Wainwright TW

Aims

The evidence base within trauma and orthopaedics has traditionally favoured quantitative research methodologies. Qualitative research can provide unique insights which illuminate patient experiences and perceptions of care. Qualitative methods reveal the subjective narratives of patients that are not captured by quantitative data, providing a more comprehensive understanding of patient-centred care. The aim of this study is to quantify the level of qualitative research within the orthopaedic literature.

Methods

A bibliometric search of journals’ online archives and multiple databases was undertaken in March 2024, to identify articles using qualitative research methods in the top 12 trauma and orthopaedic journals based on the 2023 impact factor and SCImago rating. The bibliometric search was conducted and reported in accordance with the preliminary guideline for reporting bibliometric reviews of the biomedical literature (BIBLIO).