|Year : 2016 | Volume
| Issue : 2 | Page : 44-50
Treatment of intertrochanteric femoral fracture with proximal femoral medial sustainable intramedullary nails: study protocol for a randomized controlled trial
Peng-bin Yin, An-hua Long, Jing Shen, Pei-fu Tang
Department of Orthopedics, Chinese PLA General Hospital, Beijing, China
|Date of Web Publication||31-May-2016|
Department of Orthopedics, Chinese PLA General Hospital, Beijing
Source of Support: None, Conflict of Interest: None
Background: Conservative management of intertrochanteric femoral fracture often yields poor therapeutic outcomes, and surgical fixation is generally warranted. Biomechanical instability of intertrochanteric femoral fracture is a major cause of fixation failure. To increase the stability of intramedullary nails in intertrochanteric femoral fracture, it is critical to strengthen the support between the nail and the cortical bone. Our previously designed proximal femoral medial sustainable intramedullary nail has been proven to be able to provide this internal support and stabilization by finite element analysis. We aim to examine the efficacy and safety of internal fixation with this new type of intramedullary nail in the treatment of stable and unstable intertrochanteric femoral fractures.
Methods/Design: This will be a single-center, two-arm, parallel, randomized controlled trial conducted at the Chinese PLA General Hospital, China. Seventy-two patients with stable or unstable intertrochanteric femoral fracture diagnosed according to AO/OTA Classification of Fractures and Dislocations will be randomly assigned to receive internal fixation either with proximal femoral medial sustainable intramedullary nails, or proximal femoral nail antirotation. The primary outcome measure will be bone healing condition 6 months postoperatively; secondary outcomes will be requirement for revision surgery, quality of life and complications 1 year postoperatively.
Discussion: Our findings will provide an evidence base for the use of proximal femoral medial sustainable intramedullary nails for the treatment of intertrochanteric femoral fracture.
Trial registration: ClinicalTrial.gov identifier: NCT01437176; registered on 1 September 2011.
Ethics: This protocol was approved by Ethics Committee of Chinese PLA General Hospital of China (approval No. 07/06/2011) and will be performed in accordance with the Declaration of Helsinki formulated by the World Medical Association.
Informed consent: Written informed consent will be obtained prior to involvement in the clinical trial.
Keywords: clinical trial; fracture; intertrochanteric femoral fracture; internal fixation; intramedullary nail; proximal femoral medial sustainable intramedullary nail; proximal femoral nail antirotation; randomized controlled trial
|How to cite this article:|
Yin Pb, Long Ah, Shen J, Tang Pf. Treatment of intertrochanteric femoral fracture with proximal femoral medial sustainable intramedullary nails: study protocol for a randomized controlled trial. Clin Trials Orthop Disord 2016;1:44-50
|How to cite this URL:|
Yin Pb, Long Ah, Shen J, Tang Pf. Treatment of intertrochanteric femoral fracture with proximal femoral medial sustainable intramedullary nails: study protocol for a randomized controlled trial. Clin Trials Orthop Disord [serial online] 2016 [cited 2021 Jan 16];1:44-50. Available from: https://www.clinicalto.com/text.asp?2016/1/2/44/183001
| Background|| |
As society ages rapidly, the incidence of osteoporosis-related intertrochanteric femoral fracture is increasing. Intertrochanteric femoral fracture often results in severe bleeding, and treatment may be complicated by femoral head extrusion and lower limb deformity. Conservative treatment for proximal femoral fracture does not generally achieve good clinical outcomes, especially in the elderly, who are more likely to encounter complications (Jain et al., 2003). Consequently, surgical fixation is the preferred treatment; surgical intervention reportedly accelerates recovery and reduces the likelihood of complications that arise as a result of long-term bed rest (Bergeron et al., 2009).
Internal fixation devices commonly used for intertrochanteric femoral fracture are mostly either extramedullary implants with a dynamic condylar screw (Crawford et al., 2006) and proximal femoral locking plate, or intramedullary implants such as the Gamma nail and proximal femoral nail antirotation (PFNA). It has been long discussed which method can achieve a better result.
Recently, internal fixation with an intramedullary nail is becoming increasingly popular, particularly in the treatment of unstable intertrochanteric femoral fracture (de Vries et al., 2006; Kuzyk et al., 2009a). Internal fixation with an intramedullary nail is quicker, results in less perioperative trauma and blood loss, and provides stronger long-term biomechanical stability (Kuzyk et al., 2009b). If an intertrochanteric femoral fracture is unstable, internal fixation with an intramedullary nail provides sufficient biomechanical stability to allow early postoperative weight-bearing exercise (Simmermacher et al., 2008; Yli-Kyyny et al., 2012). Nonetheless, internal fixation with currently available intramedullary nails may be complicated by internal fixation failure and other implant-related complications, such as bending and segmentation of the intramedullary nail, coxa vara and femoral stem fracture; the failure rate is particularly high after fixation of severely comminuted and unstable intertrochanteric femoral fractures.
The PFNA is a novel proximal femoral nail based on designs by the Association for Osteosynthesis/Association for the Study of Internal Fixation (AO/ASIF) and is used for the treatment of proximal femoral fractures; it provides strong anti-rotation and angle stability (Helwig et al., 2009). The system is characterized by the ability to apply cement through its helical perforated blade, increasing the tensile force for stabilization and avoiding rotation and inward collapse. In addition, distal inclined locking can reduce stress concentration and decrease the risk of distal fracture (Mereddy et al., 2009). Although the incidence of postoperative greater trochanteric pain syndrome after internal fixation with PFNA is reportedly as high as 10%, Pu et al. (2009) have suggested that this might be a consequence of the proximal femoral anatomy of Chinese people causing the screw to protrude from the greater trochanter. Unfortunately, screw withdrawal can exacerbate greater trochanteric pain syndrome, destabilize the biomechanical properties of the proximal femur, and cause avascular necrosis, malunion and refracture of the femoral head (Seral et al., 2004). Biomechanical instability is a major cause of fixation failure. The fixation stability of the intramedullary nail in intertrochanteric femoral fracture can be increased by strengthening the interaction between the intramedullary nail and the cortical bone. Our previously designed noval proximal femoral medial sustainable intramedullary nail has been proven to be able to provide internal support and stabilization, and would be expected to reduce screw cutting, femoral head rotation and the incidence of coxa vara. To the best of our knowledge, the efficacy of internal fixation of stable and unstable intertrochanteric femoral fracture with this new type of intramedullary nail has not been examined. Here, we describe a study that will examine the efficacy and safety of internal fixation with this new type of intramedullary nail in the treatment of stable and unstable intertrochanteric femoral fracture.
| Methods/Design|| |
This will be a single-center, two-arm, parallel, randomized controlled trial. It will be performed at the Chinese People's Liberation Army (PLA) General Hospital, China. Seventy-two patients with stable or unstable intertrochanteric femoral fracture diagnosed according to the AO/OTA Classification of Fractures and Dislocations will be randomly assigned to undergo internal fixation with either a proximal femoral medial sustainable intramedullary nail or a PFNA. The primary outcome measure will be bone healing condition, assessed by X-ray, 6 months after surgery. The secondary outcome measures will be requirement for revision surgery, quality of life and complications arising 1 year after surgery. A flow chart of the trial protocol is shown in [Figure 1].
|Figure 1: Flow chart of the trial protocol. |
Note: NTIN: New-type intramedullary nail (i.e., proximal femoral medial sustainable intramedullary nail); PFNA: proximal femoral nail antirotation.
Click here to view
Eligible patients with stable or unstable intertrochanteric femoral fracture will be recruited from the Division of Traumatic Disease, Department of Orthopedics, Chinese PLA General Hospital, China.
Patients of either sex who meet all the following criteria will be recruited:
- Age > 18 years
- Diagnosed with intertrochanteric femoral fracture by anteroposterior and lateral radiographs and advanced computed tomography or magnetic resonance imaging techniques
- Unilateral intertrochanteric femoral fracture
- Recent closed fracture (surgical intervention within 2 weeks of emergency admission)
- Patients were ambulatory before fracture, though they many have used a walking aid such as a cane or frame
- Anticipated medical optimization with operative fixation of the hip
- Able to tolerate anesthesia and surgery
- No other severe trauma
- Able to provide informed consent
Patients with any of the following conditions will be excluded:
- Patients not suitable for internal fixation (severe osteoarthritis, rheumatoid arthritis or pathological fracture)
- Associated major injuries of the lower extremity (i.e., ipsilateral or contralateral fractures of the foot, ankle, tibia, fibula, knee or femur; dislocation of the ankle, knee or hip; or femoral head defects caused by fracture)
- Retained hardware around the affected hip
- Infection around the hip (i.e., soft tissue or bone)
- Patients with disorders of bone metabolism other than osteoporosis (i.e., Paget's disease, renal osteodystrophy or osteomalacia)
- Patients with moderate or severe cognitive impairment (Six Item Screener with three or more errors)
- Patients with Parkinson's disease (or dementia) severe enough to increase the likelihood of falling or severe enough to compromise rehabilitation
- Poor compliance
- Patients judged by the research team not to be suitable for participation due to difficulty with follow up, for example having no fixed address, plans to move away within the next year or intellectual impairment without adequate family support.
According to the AO/OTA Classification of Fractures and Dislocations (Bosse et al., 2001), stable intertrochanteric femoral fracture is classified as below A2.1 (with 2.1) and unstable intertrochanteric femoral fracture as above A2.1 (without A2.1). Patients with either fracture type will be randomly assigned by a researcher using computerized randomization method to undergo internal fixation either with a PFNA or proximal femoral medial sustainable intramedullary nail, a new-type intramedullary nail (NTIN). The randomly generated numbers and assignments will be preserved in an opaque sealed envelope and will not be disclosed until eligible patients have agreed to participate in the trial. If any error or disclosure with regard to randomization occurs, a new randomization sequence will be generated starting from the problematic serial number and allocated to subsequent patients. Patients will be blinded to information regarding grouping and intervention, but the researcher responsible for surgery will know the grouping.
Implantation of PFNA
According to the degree and direction of fracture displacement, the affected limb will be subject to skin traction and fixation in a neutral position. Anteroposterior radiographs of the pelvis and lateral radiographs of both hips will be taken to clarify the fracture type and measure the diameter of the contralateral medullary cavity to determine the diameter of the PFNA (Shandong Weigao Orthopedic Device Company Limited, Weihai, China) and the length of proximal and distal interlocking intramedullary nails. Prophylactic antibiotics will be administered 30 minutes before surgery. The patients will be positioned supine on an extension table with the capacity for lower limb traction. Under general or epidural anesthesia and after traction of the affected lower limb, the unaffected lower limb will be extended, abducted or subject to slight countertraction in abduction and extorsion.
Closed traction and reduction will be performed under X-ray guidance. After reduction, a 3-6 cm longitudinal incision will be made above the vertex of the greater trochanter to expose the top of the greater trochanter. The PFNA entry point will be selected slightly lateral to the tip of the greater trochanter. The medullary canal will be opened, enlarging the entrance to facilitate the insertion of the thick tail of the PFNA ([Figure 2]). After a guide wire has been inserted into the medullary canal and its position confirmed by fluoroscopy (expansion of the medullary canal will not be undertaken in most patients with osteoporosis), a gunsight-equipped properly-sized PFNA blade will be slowly screwed into the proximal femoral medullary canal. The insertion depth and declination of the PFNA blade will then be adjusted. A guide pin will be inserted via the proximal locking pore of the gunsight. After the insertion position of the guide pin has been confirmed by fluoroscopy, a hole will be drilled to penetrate the lateral cortex using a cannulated drill along the guide pin. A properly sized screw blade held in an inserter will be impacted along the guide pin in an anticlockwise direction. The inserter will be rotated in a clockwise direction so that the screw blade compresses the fracture fragments, the screw blade will be locked, and generally a distal locking screw will be positioned. After satisfactory internal fixation is confirmed on fluoroscopy in the anteroposterior view, the end cap will be inserted. After irrigation of the surgical site, the skin will be closed with sutures.
Implantation of proximal femoral medial sustainable intramedullary nail
The implantation procedure of the NTIN (Shandong Weigao Orthopedic Device Company Limited, China; patent number ZL201020121021.6; [Figure 3]) will be similar to that of the PFNA, except that after positioning of the screw blade, the limit screw will be fastened to lock the sleeve, and the sustainable nail will be inserted through the guide sleeve and fastened. As for PFNA implantation, a distal screw will be inserted for static locking.
|Figure 3: Proximal femoral medial sustainable intramedullary nail (new-type intramedullary nail).|
Click here to view
Bone healing condition evaluated by X-ray examination 6 months after treatment.
All were assessed 12 months after treatment:
- Requirement for revision surgery
- Quality of life quantified using the Medical Outcomes Study 36-item Short Form Health Survey (MOS SF-36) score (Farivar et al., 2007), Activities of Daily Living (ADL) Scale score (Shinar et al., 1987) and Functional Independence Measure (FIM) score (Stineman et al., 1996)
- Complications (mortality, nonunion, implant breakage/failure, infection, deep vein thrombosis)
The timing of trial outcome measures is shown in [Table 1].
Withdrawal of treatment
If patients exhibit severe adverse events, are potentially pregnant or subsequently fulfil any of the exclusion criteria after enrollment, researchers will determine whether the patient should be withdrawn from the trial according to their experience. Related data from these patients will be subject to intention-to-treat analysis unless patients request their data are discarded. The reason for trial withdrawal will be recorded in the case report form and medical case notes.
Withdrawal of consent of follow-up
If patients or their relatives decline to undergo follow-up, the patients will be withdrawn from the trial and data collected before withdrawal will only be included in the final analysis after acquiring informed consent.
Criteria for withdrawal from treatment
Upon the request of the researcher or patients due to safety concerns; patients who have no fixed address; those who report a plan to move away in the next year, or intellectually impaired patients without adequate family support.
Any expected or unexpected adverse events will be recorded. The occurrence of complications and severe adverse events will be recorded as secondary endpoints. Expected complications include postoperative delayed femoral shaft fracture on the affected side, screw loosening, delayed union, malunion, bone nonunion and other related postoperative complications including secondary infection, pressure sores, venous thrombosis and pneumonia. If severe adverse events occur, detailed information of the adverse events including the date of occurrence, measures taken related to the treatment, causal relationship with the treatment and treatment of the adverse event will be declared to the researchers responsible for the trial and the ethics committee.
Paper case report forms with complete information will be preserved in a secure locked environment for future viewing. Data will be input into an electronic database by professional staff using a double-data entry strategy. Conduct of the trial will be monitored by a professional research associate to ensure patient safety and data integrity; for example, it will be established that the correct consented procedure was undertaken, primary endpoints were evaluated and that patients were compliant. The research associate will have access to all essential documents. In addition to regular site visits, the research associate will liaise with the trial center via e-mail or telephone.
Each patient will be allocated a unique trial number. Paper case report forms will be preserved in a secure and locked location in accordance with local data protection laws and regulations. During clinical visits, the research associate will check each patient's related data to ensure that data preservation is compliant with data protection laws and regulations, and to ensure data accuracy and integrity.
All data will be analyzed by professionals using SPSS 15.0 software (SPPS Inc., Chicago, IL, USA). Classification variables will be expressed as proportions, and measurement data as the mean ± standard deviation. For general clinical data, the chi-square test will be used to compare numeration data between the two study groups, and Student's t-test will be used to compare measurement data. The paired t-test will be to compare individual patient's measurement before and after treatment. A P value < 0.05 will be considered statistically significant.
| Discussion|| |
The optimal surgical therapeutic strategy for intertrochanteric femoral fracture is still not known, particularly when cortical bone is deficient in the femoral neck (Schipper et al., 2004), but the NTIN appears to have substantial potential. In an antirotation intensity test, the blade of the PFNA holds the femoral head and neck, while the medial sustainable nail anchors the blade and the fracture fragments are reduced and fixed by a plane made by the locking bolt and locking screws, providing stability against antirotation. When reducing and fixing fracture fragments using NTIN medial sustainable nails, we believe that the plane of the nail affords even greater anti-rotatory properties (Han, 2014).
We aim to inform the evidence base for the rational use of the proximal femoral medial sustainable intramedullary nail (NTIN) in the treatment of intertrochanteric femoral fracture.
Recruiting is ongoing at the time of submission.
In April 2015, the team led by PFT developed a method to measure the proximal femur in three dimensions using computer-aided design software, including Mimics, and used this method to analyze the anatomic morphology of the proximal femur after internal fixation with an InterTan intramedullary nail or a PFNA. They found that the change in anteversion of the femoral neck was greater after internal fixation with a PFNA than with an InterTan intramedullary nail, and there was a strong correlation between the anteversion of the two types of intramedullary nails and the anteversion of the femoral neck on the affected side. In the same year, they also conducted a study to compare the therapeutic effects of internal fixation with PFNA and InterTan nails in 178 elderly patients with intertrochanteric femoral fracture, examining the duration of surgery and hospitalization, the amount of intraoperative bleeding, postoperative complications, bone healing time and functional recovery (using Harris scores). They concluded that PFNA was superior for intertrochanteric femoral fracture in elderly patients with osteoporosis, and that this method was more suitable for unstable intertrochanteric femoral fracture in young patients. 
Conflicts of interest
PFT conceived and designed this trial protocol. PBY and AHL helped to develop the study measures and analyses.JS wrote the paper. All authors approved the final version of this paper for publication.
This paper was screened twice using CrossCheck to verify originality before publication.
This paper was double-blinded and stringently reviewed by international expert reviewers.
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[Figure 1], [Figure 2], [Figure 3]
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