Keywords
dynamic hip screw, hip fracture, intracapsular, neck of femur, sliding hip screw, derotation screw,
dynamic hip screw, hip fracture, intracapsular, neck of femur, sliding hip screw, derotation screw,
Intracapsular neck of femur (NOF) fractures comprise one of the most common orthopaedic injuries1. The majority are treated with arthroplasty, as the femoral neck biomechanics and vulnerability of the blood supply lead to a high incidence of non-union and avascular necrosis following internal fixation. Some may be treated with fixation rather than replacement depending on patient factors and fracture configuration, however, the optimal fixation method is controversial2.
The choice of fixation method for intracapsular fractures is either cannulated hip screws (CHS), or dynamic hip screw (DHS) with or without a derotation screw (DRS). These devices provide stability in the plane of the femoral neck, whilst enabling compression at the fracture site to facilitate direct healing.
The biomechanics of basicervical fractures are influenced by fracture character and fixation method. Stankewich et al. (1996) investigated the biomechanical impact afforded to fracture configuration under cyclical and failure loading. They determined that force at the fracture site correlates with fracture angle. The more vertical the fracture angle, the greater the force resisted by the implant alone, and ultimate failure force correlated with the moment arm3.
The load through the hip when walking at 4km/h is approximately 238% body weight (BW), increasing to 250% when ascending stairs and 260% when descending4. Therefore a 70kg person loads the hip with approximately 1400–1500N when walking. The torsional force through the femur is also 23–83% larger when climbing stairs than when walking4. Using synthetic femurs Freitas et al. (2014) compared the load to failure for a pauwels III fracture fixed with a DHS plus DRS against a control group without fracture and found the mean load to failure in the DHS group was 1742N, compared to 1329N in the control group5.
Blair (1994) states that a DRS provides rotational control during insertion of the lag screw, but no additional fixation thereafter6. This opinion is echoed by both clinical experience of others7,8 and biomechanical testing by Swiontkowski et al. (1987)9. However, biomechanical studies of cadaveric fractures have shown that DHS with DRS gives superior stabilisation, theoretically reducing AVN and non-union10,11.
In this study we examine the impact employing a permanent derotation screw concomitantly with a 2-hole DHS has on rate of revision to arthroplasty in the treatment of intracapsular NOF fractures.
A list of 161 patients were identified as sustaining an intracapsular NOF fracture treated with internal fixation between April 2009 and April 2014. The patient follow-up notes and imaging were reviewed, excluding those treated with CHS, and ensuring follow up for at least one year. This left 64 patients treated with DHS, 28 of those treated with a derotation screw (the DRS group), and 36 without (the non-DRS group).
X-rays, operation notes, discharge summaries and clinic letters were reviewed to assess the outcomes associated with the treatments. Each fracture was assessed and scored using Pauwels and Gardens classifications1 to ensure homogeneity between the DRS group and the non-DRS group with regards to fracture severity. The follow-up was reviewed and a negative outcome was defined as the need for revision surgery to hip arthroplasty.
The following inclusion criteria were applied:
Patient demographics between the groups are summarised in Table 1. The Pauwels and Gardens scores are shown in Table 2 and Table 3. Pauwels score cut-offs are 0–30° for 1, 30–50° for 2 and >50° for 312. The mean fracture angle in the DRS group was 39.78 degrees (SD 11.11) compared to 35.18 degrees (SD 9.69) in the non-DRS group, and the proportion of each fracture character in the 2 groups shows a similar distribution. We therefore determined that the groups were sufficiently homogeneous to allow comparison.
DRS: permanent derotation screw.
The patients in the DRS group had a significantly lower rate of revision to arthroplasty than those in the non-DRS group (p=0.0203), as shown in Table 4. Without a derotation screw the revision rate was 39%, in comparison to 14% when a DRS was used.
N=64 | Derotation screw | No derotation screw | |
---|---|---|---|
No Revision | 24 (76%) | 22 (61%) | |
Revision | 4 (14%) | 14 (39%) | P=0.0299 |
Employing a permanent derotation screw alongside a dynamic hip screw seems to offer protection against requirement for revision to arthroplasty, carrying a relative risk reduction of 66% and NNT of 4.06. This NNT suggests the clinical impact of routinely employing a DRS could be quite significant, and needs to be further investigated with robust, prospective clinical studies. To the best of the our knowledge, there are no previous studies analysing the impact a derotation screw has on the failure rate of 2-hole sliding hip screws when used for treating intracapsular hip fractures.
Of the 18 patients requiring revision, 16 underwent total hip arthroplasty, 1 underwent hemiarthroplasty and one (in the non-DRS group) was managed conservatively despite requiring revision. We included this patient as it was documented that they required revision to arthroplasty, but were not fit for surgery, and therefore met our definition of a negative outcome.
When reviewing images it was not possible to ascertain whether an intraoperative derotation wire had been used as these images were rarely saved, and operative notes were unreliable in reporting this. Our non-DRS group therefore likely contained some patients that were covered with an intraoperative derotation wire and some that were not.
This study shows a reduced rate of revision to arthroplasty when a permanent DRS was used alongside a 2-hole DHS for fixation of intracapsular neck of femur fractures when compared to DHS alone. Given effect size suggested in this study and potential improvements in patient care that could be achieved we recommend this is an area that should be investigated with a randomised controlled trial.
Dataset 1: Source data used as a basis for the findings in this study. Data collected for this study was collected through Hull Royal Infirmary’s hip fracture database, which is gathered for the national hip fracture database (NHFD). DOI, 10.5256/f1000research.11433.d16127013.
All data collected for this study was collected through Hull Royal Infirmary’s hip fracture database, which is gathered for the national hip fracture database (NHFD). From the NHFD website: "the NHFD is approved by the NHS England HRA Confidentiality Advisory Group (CAG) to collect patient data without consent under Section 251 exemption. (This approval was formerly administered under the NIGB-ECC/PIAG)." and "patients do not need to give formal consent" for data to be collected, but “may opt out if they wish”.
SW, lead researcher and author, designed the study, collected data, analysed data and performed the write up. RP performed background research and contributed to the write up. IV assisted with data collection and analysis. AA-M obtained patient lists and internal permissions. RM oversaw the project.
Supplementary File 1: Statistical analysis of the source data summarising the main findings. Statistics were calculated using SPSS.
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Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
No
Are sufficient details of methods and analysis provided to allow replication by others?
No
If applicable, is the statistical analysis and its interpretation appropriate?
Partly
Are all the source data underlying the results available to ensure full reproducibility?
Partly
Are the conclusions drawn adequately supported by the results?
No
Competing Interests: No competing interests were disclosed.
Is the work clearly and accurately presented and does it cite the current literature?
Yes
Is the study design appropriate and is the work technically sound?
Yes
Are sufficient details of methods and analysis provided to allow replication by others?
No
If applicable, is the statistical analysis and its interpretation appropriate?
Partly
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Partly
Competing Interests: No competing interests were disclosed.
Is the work clearly and accurately presented and does it cite the current literature?
Yes
Is the study design appropriate and is the work technically sound?
No
Are sufficient details of methods and analysis provided to allow replication by others?
No
If applicable, is the statistical analysis and its interpretation appropriate?
No
Are all the source data underlying the results available to ensure full reproducibility?
Yes
Are the conclusions drawn adequately supported by the results?
Partly
Competing Interests: No competing interests were disclosed.
Alongside their report, reviewers assign a status to the article:
Invited Reviewers | |||
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1 | 2 | 3 | |
Version 1 15 May 17 |
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