Three Dimensional Digital Preoperative Planning for the Osteosynthesis of Distal Radius Fractures

April 25, 2022 updated by: Yuichi Yoshii, Tokyo Medical University

Background: Three dimensional (3D) digital pre-operative planning software for osteosynthesis of fractures was developed. To assess the usefulness of the 3D planning, we evaluated the accuracy of the reduction shapes and selected implants in the patients with distal radius fractures.

Methods: Thirty wrists of 30 distal radius fracture patients who underwent osteosynthesis using volar locking plates were evaluated. Fifteen wrists were treated with 3D preoperative planning as the plan group. The other fifteen wrists were treated with conventional preoperative planning as the control group. Volar tilt and radial inclination were measured after operation and compared with the healthy side wrist. In addition, preoperative planning and postoperative reductions were compared by measuring the volar tilt and radial inclination of the 3D images in the plan group. The intra-class correlation coefficient (ICC) values of the radiological parameters between healthy side wrists and injured side wrists, between preoperative planning and postoperative reductions were evaluated. For the accuracy of the implant choices, the ICCs for the screw lengths between the preoperative plan and the actual choices were evaluated in the plan group.

Study Overview

Detailed Description

Patients and Methods The study protocol was approved by our Institutional Review Board. Thirty wrists of 30 distal radius fracture patients who underwent osteosynthesis using locking plates (19 females, 11 males; age range 23-89, mean age 59.5 years) were evaluated. Patients were excluded if they reported a previous history of traumatic injuries to the arm. The patients were divided into two groups: 15 patients in the plan group utilized our 3D digital preoperative planning software, and 15 patients in the control group utilized standard preoperative assessment on plain radiographs and CT scans. The age, sex, and fracture types were matched between groups. According to the preoperative CT scans, fractures were classified using the AO classification system.

Preoperative Planning In the plan group, 3D digital preoperative planning and a surgical simulation were performed in order to determine the reduction and the placement of the implants in addition to the plate/screw size prior to surgery. Reduction and placement of the implants were simulated using software newly-developed by the authors (Zed-Trauma, LEXI Co., Ltd. Tokyo, Japan). Planning using this software is based on digital imaging and communications in medicine (DICOM) data from CT scans. All preoperative planning group patients had pre- and post-operative CT scans in order to compare the planned and post-operative reduction shape and placement of the implant. The CT comprised contiguous sections of 1 mm thickness. The software allows the surgeons to 1) visualize the fracture displacement, 2) simulate repositioning of the fragments, 3) place the plate and screws, 4) adjust the sizes of the implants, and 5) check the shape after the reduction and implant placement by measuring anatomical shape (Figure 1 and 2). After importing the DICOM images to the software, a 3D image of the distal radius was made. Each distal radius fracture was segmented according to the main fracture fragments using the cut function. Each fragment was repositioned in accordance with fracture lines. After repositioning the fragments, the bone shape was checked three dimensionally. Reduction of the fragment was performed to regain the volar tilt and the radial inclination, and less than 2mm step-off for the intra-articular displacement referring to the healthy side wrist X ray. Simulation of the implantation of the volar locking plate used 3D templates with variable sizes of plates and screws. The Stellar II locking plate (HOYA Technosurgical, Inc., Tokyo, Japan) was used in this study. This plate system has small, medium, and large sizes for the width, and short and long sizes for the plate length. Screw lengths from 10 to 24 mm for the distal (2.4 mm diameter), and 10 to 20 mm for the proximal (2.6 mm diameter) are available. Computer aided design models of different-sized implants were installed in the software. The plate size was chosen to cover the distal fragment maximally and not exceeded the width of the distal radius. The plans were made by a single hand surgeon. After the planning, osteosynthesis was performed under general anesthesia. During the surgery, the operator performed the reduction and the placement of the plate while comparing images between the preoperative plan and fluoroscopy. The surgeons tried to reproduce the planned position of the implant by checking the distances from the margin of the implant to the margin of the radius under fluoroscopy. The screw sizes were determined by intraoperative measurement in reference to the preoperative plan. For the screw fixation, a guide block was used to insert the distal screws.

In the control group, preoperative planning was performed using conventional posterior-anterior and lateral view radiographs. Based on the X-ray image, the plate size was chosen using the conventional template. After the planning, osteosynthesis was performed under general anesthesia in the same manner as for the plan group. The surgeries were performed by several residents and fellows under supervision of a hand surgeon.

Evaluations The planned sizes of implant were compared with the actual sizes used at operation in the plan group. The screw holes were numbered from 1 to 8 for the distal (there were 7 holes in small and medium plates, and 8 holes in a large plate), and from 1 to 3 for the proximal. The screw lengths actually chosen were recorded according to the screw number.

To evaluate the accuracy of the anatomical reduction, volar tilt and radial inclination of the post-operative wrists X-ray were compared with those of the healthy side wrist in both plan and control groups. The posterior-anterior view was obtained with the elbow flexed at 90°, the ulna perpendicular to the humerus, and the forearm in the pronated position. The lateral view was obtained with the elbow flexed at 90° and adducted against the trunk. The wrists were in a neutral position with no flexion, extension, or deviation in either view. Volar tilt was measured on a lateral view. The angle between a line along the distal radial articular surface and the line perpendicular to the longitudinal axis of the radius at the joint margin was measured as volar tilt. Radial inclination was measured on a posterior-anterior view. The angle between one line connecting the radial styloid tip and the ulnar aspect of the distal radius and a second line perpendicular to the longitudinal axis of the radius was measured as radial inclination. These radiological parameters were measured by a single hand surgeon. In addition, preoperative planning and postoperative reductions were compared by measuring the volar tilt and radial inclination of the 3D images in the plan group (Figure 3). The axis of the radius was adjusted. The angle between a line from the dorsal edge to the volar edge of the radius and the line perpendicular to the longitudinal axis of the radius was measured as 3D volar tilt. The angle between a line from the radial styloid tip to the ulnar aspect of the distal radius and the line perpendicular to the longitudinal axis of the radius was measured as 3D radial inclination.

Statistical Analysis The results are expressed as mean +/- standard deviation. An intra-class correlation coefficient (ICC) was used to evaluate the accuracy of the anatomical reduction. The ICC values of the radiological parameters (volar tilt and radial inclination) between healthy side wrists and injured side wrists after the surgery were evaluated in both the plan and control groups. In addition, the ICCs of the 3D measurements between the pre-operative plan and the post-operative 3D images were evaluated in the plan group.

For the accuracy of the implant choices, the ICCs for the screw lengths between the preoperative plan and the actual choices were evaluated. According to the previous recommendation12, ICC less than 0.40 was considered poor reproducibility, between 0.40 and 0.59 was considered moderate, between 0.60 and 0.74 was considered good, and between 0.75 and 1.00 was considered excellent. The differences between preoperative plan and postoperative reductions, healthy side and injured side after surgery were analyzed using the paired t-test. P values of <0.05 were considered significant. All analyses were performed using SPSS version 13.0 (SPSS, Chicago, IL, USA).

Study Type

Interventional

Enrollment (Anticipated)

100

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Ibaraki
      • Ami, Ibaraki, Japan, 300-0395
        • Recruiting
        • Tokyo Medical University Ibaraki Medical Center
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • the patients who have distal radius fracture in their unilateral wrist.

Exclusion Criteria:

  • the patients who reported a previous history of traumatic injuries to the arm.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: NON_RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Plan group
3D preoperative planning for the distal radius fracture was performed prior to the osteosynthesis.
preoperative planning using 3D digital planning software or conventional template
osteosynthesis using volar locking plate
Active Comparator: Control group
Conventional preoperative planning for the distal radius fracture was performed prior to the osteosynthesis.
preoperative planning using 3D digital planning software or conventional template
osteosynthesis using volar locking plate

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Intraclass correlation coefficients between preoperative plan and after surgery
Time Frame: 1 week
An intra-class correlation coefficient (ICC) was used to evaluate the accuracy of the anatomical reduction. The ICC values of the radiological parameters (volar tilt and radial inclination) between healthy side wrists and injured side wrists after the surgery were evaluated in both the plan and control groups. In addition, the ICCs of the 3D measurements between the pre-operative plan and the post-operative 3D images were evaluated in the plan group.
1 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Yuichi Yoshii, Tokyo Medical University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2014

Primary Completion (Anticipated)

May 1, 2024

Study Completion (Anticipated)

May 1, 2025

Study Registration Dates

First Submitted

September 14, 2016

First Submitted That Met QC Criteria

September 16, 2016

First Posted (Estimate)

September 21, 2016

Study Record Updates

Last Update Posted (Actual)

April 27, 2022

Last Update Submitted That Met QC Criteria

April 25, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 14-21

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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