CN111400953A - Simulation system for distraction osteogenesis - Google Patents
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Abstract
Description
技术领域:Technical field:
本发明涉及数值模拟仿真技术领域,具体涉及一种牵张成骨的仿真系统。The invention relates to the technical field of numerical simulation, in particular to a simulation system for distraction osteogenesis.
背景技术:Background technique:
牵张成骨术是通过截骨术将骨骼切开,利用牵张器对骨组织施加稳定和缓慢的牵张力以刺激组织细胞的再生和生长,促进牵张间隙中新骨形成和矿化,从而达到延长骨骼的目的。目前临床上牵张成骨术最大的缺陷在于新骨形成和矿化缓慢,导致牵张器滞留时间久、治疗周期漫长,给患者的生活和工作带来了极大的不便。据临床报道,牵张成骨术治疗下肢(股骨和胫骨)骨缺损所需的牵张支架固定时间可达10个月到3年。另外,约35%~68%的牵张成骨手术存在骨愈合延迟或不愈合等问题。因此,研究如何加速牵张成骨术中新骨形成和矿化进而缩短治疗周期具有非常重要的临床实用价值。牵张成骨新骨形成和矿化的快慢取决于所施加的牵张模式(如牵张期牵张速率、牵张期牵张频率、牵张期持续时间、巩固期施加牵-压耦合刺激时期、牵-压耦合载荷施加速率、牵压耦合载荷施加频率和牵张器刚度等),但目前牵张模式的选择大都基于医生经验,尚没有一种可供医生术前选择最佳牵张模式的工具。Distraction osteogenesis is to cut the bone through osteotomy, and use the distractor to apply stable and slow distraction to the bone tissue to stimulate the regeneration and growth of tissue cells, and promote the formation and mineralization of new bone in the distraction gap. So as to achieve the purpose of lengthening the bones. At present, the biggest drawback of distraction osteogenesis in clinical practice is the slow formation and mineralization of new bone, which leads to a long retention time of the distractor and a long treatment period, which brings great inconvenience to the life and work of patients. According to clinical reports, distraction stent fixation time required for the treatment of lower extremity (femur and tibia) bone defects by distraction osteogenesis can range from 10 months to 3 years. In addition, about 35% to 68% of distraction osteogenesis have problems such as delayed or non-union of bone union. Therefore, it is of great clinical and practical value to study how to accelerate the formation and mineralization of new bone in distraction osteogenesis to shorten the treatment period. The rate of new bone formation and mineralization during distraction osteogenesis depends on the applied distraction mode (eg, distraction rate, distraction frequency, distraction duration, and application of coupled distraction-compression stimulation during consolidation). period, traction-compression coupled load application rate, traction-compression coupled load application frequency, and stretcher stiffness, etc.), but currently, the choice of stretch mode is mostly based on doctor’s experience, and there is no one available for doctors to choose the best stretch before surgery. pattern tool.
牵张成骨系统仿真通过建立力学生物学模型,以程序的方式来模拟和展示牵张力学刺激作用下骨再生的动态过程和成骨结果。应用计算机仿真技术对牵张成骨进行模拟,设置不同的牵张组合加载参数,再现牵张成骨术中复杂的骨再生动态过程,方便医生寻找针对临床对象的最佳牵张模式,有助于缩短牵张成骨治疗周期,降低并发症的发生率。The simulation of the distraction osteogenesis system simulates and displays the dynamic process of bone regeneration and osteogenic results under the stimulation of distraction mechanics in a procedural manner by establishing a mechanobiological model. Using computer simulation technology to simulate distraction osteogenesis, setting different distraction combined loading parameters, reproducing the complex dynamic process of bone regeneration in distraction osteogenesis, it is convenient for doctors to find the best distraction mode for clinical objects. It can shorten the period of distraction osteogenesis and reduce the incidence of complications.
发明内容:Invention content:
本发明的目的在于提供一种牵张成骨的仿真系统,可以针对患者的个性化仿真模型,描述截骨区域骨痂的粘弹塑性行为,利用模糊逻辑实现基于应变调控的组织分化进行数值分析,再现牵张成骨术中复杂的骨再生动态过程,方便医生寻找针对患者的最佳力学刺激条件,有助于缩短整个治疗时间,进而降低并发症的发生率。The purpose of the present invention is to provide a simulation system for distraction osteogenesis, which can describe the viscoelastic-plastic behavior of the callus in the osteotomy area according to the patient's personalized simulation model, and use fuzzy logic to realize the tissue differentiation based on strain regulation for numerical analysis , reproduce the complex dynamic process of bone regeneration in distraction osteogenesis, facilitate doctors to find the best mechanical stimulation conditions for patients, help to shorten the entire treatment time, and thus reduce the incidence of complications.
为了达到上述目的,本发明提供一种牵张成骨的仿真系统,所述牵张成骨的仿真系统依据牵张成骨实施过程中,施加不同的牵张条件会引起骨痂区域组织不同的成骨效应;通过对牵张成骨的骨再生过程进行仿真计算,根据输出的成骨结果判定最佳的牵张加载模式;In order to achieve the above object, the present invention provides a simulation system for distraction osteogenesis. The simulation system for distraction osteogenesis is based on the fact that during the implementation of distraction osteogenesis, applying different distraction conditions will cause different tissue in the callus area. Osteogenic effect; by simulating the bone regeneration process of distraction osteogenesis, the optimal distraction loading mode is determined according to the output osteogenesis results;
所述牵张成骨的仿真系统包括A1对象截骨区域个体化三维重建模块、A2牵张参数设置模块、A3截骨区域计算生物力学分析模块、A4骨再生动态过程模拟模块和A5显示模块;The simulation system for distraction osteogenesis includes an A1 object osteotomy area individualized three-dimensional reconstruction module, A2 distraction parameter setting module, A3 osteotomy area computational biomechanical analysis module, A4 bone regeneration dynamic process simulation module and A5 display module;
所述系统A1对象截骨区域个体化三维重建模块用于对对象截骨区域的CT图像进行自动分割并进行三维重建,得到对象截骨区域的个体化三维几何模型,然后进行网格划分处理;The system A1 object osteotomy area individualized 3D reconstruction module is used to automatically segment and perform 3D reconstruction of the CT image of the object osteotomy area, obtain an individualized 3D geometric model of the object osteotomy area, and then perform grid division processing;
所述系统A2牵张参数设置模块用于对对象个体化三维截骨区域有限元模型设置不同的力学加载模式,作为A3截骨区域计算生物力学分析模块的输入;The system A2 distraction parameter setting module is used to set different mechanical loading modes for the individualized three-dimensional osteotomy area finite element model of the object, as the input of the A3 osteotomy area computational biomechanical analysis module;
所述系统A3截骨区域计算生物力学分析模块用于依据A2牵张参数设置模块传入的加载参数,设置骨线弹性生物力学模型和骨痂区域粘弹塑性生物力学模型,进行模拟牵张确定骨痂区域的力学刺激状态;The system A3 osteotomy area computational biomechanical analysis module is used to set the loading parameters input from the A2 distraction parameter setting module, set the bone linear elastic biomechanical model and the callus area viscoelastic biomechanical model, and perform simulated distraction determination Mechanical stimulation state of the callus area;
所述系统A4骨再生动态过程模拟模块用于将有限元分析得到的应变结果作为输入,运用模糊逻辑控制,确定应变状态在组织分化图上的位置,并输出组织类型变化的结果,更新组织材料类型,再现骨痂的骨再生过程;The system A4 dynamic process simulation module of bone regeneration is used to take the strain results obtained by finite element analysis as input, use fuzzy logic control to determine the position of the strain state on the tissue differentiation map, and output the results of tissue type changes to update tissue materials type, reproducing the process of bone regeneration of callus;
所述系统A5显示模块用于显示所述牵张成骨仿真系统的计算结果。The system A5 display module is used to display the calculation results of the distraction osteogenesis simulation system.
进一步,所述A1对象截骨区域个体化三维重建模块用于得到对象截骨区域个体化的几何和有限元模型。模型由两部分组成:皮质骨和骨痂。对截骨区域有限元模型进行初始状态设置。初始状态设置包括初始皮质骨骨含量为100%、软骨含量为0%和血供为100%,初始骨痂区域骨含量为0%、软骨含量为0%和血供为0%,并将其保存在Excel文件中;Further, the individualized three-dimensional reconstruction module of the A1 osteotomy area of the object is used to obtain an individualized geometric and finite element model of the osteotomy area of the object. The model consists of two parts: cortical bone and callus. Set the initial state of the finite element model of the osteotomy area. The initial state settings include the initial cortical bone content of 100%, the cartilage content of 0% and the blood supply of 100%, the initial callus region of 0% of bone content, 0% of cartilage content and 0% of blood supply. Save in an Excel file;
进一步,通过A2设置不同的牵张加载组合参数。A2牵张参数设置模块设置参数包括:牵张期牵张速率、牵张期牵张频率、牵张期持续时间、巩固期施加牵-压耦合刺激时期、牵-压耦合载荷施加速率、牵压耦合载荷施加频率和牵张器刚度等;Further, different stretch-loading combination parameters were set through A2. The setting parameters of the A2 stretch parameter setting module include: stretch rate, stretch frequency, stretch duration, stretch-compression coupled stimulation period, stretch-compression coupled load application rate, stretch Coupled load application frequency and stretcher stiffness, etc.;
进一步,所述A3截骨区域计算生物力学分析模块用于依据A2牵张参数设置模块传入的加载参数,设置边界条件和材料属性;设置材料属性包括:在ABAQUS的用户材料设置皮质骨杨氏模量、泊松比和骨痂杨氏模量、泊松比、屈服应力、粘度系数(通过包含粘弹塑性生物力学模型的UMAT子程序进行定义材料类型),骨痂区域初始阶段被假定充满结缔组织,进行模拟牵张获得骨痂区域的力学刺激应变状态,包括:Further, the A3 osteotomy area computational biomechanical analysis module is used to set the boundary conditions and material properties according to the loading parameters input by the A2 distraction parameter setting module; setting the material properties includes: setting cortical bone Young's in the user material of ABAQUS Modulus, Poisson's ratio and Young's modulus of callus, Poisson's ratio, yield stress, viscosity coefficient (material type is defined by UMAT subroutine including viscoelastic-plastic biomechanical model), callus area is assumed to be filled at initial stage Connective tissue, perform simulated distraction to obtain mechanically stimulated strain states in the callus area, including:
B1、设置骨痂区域粘弹塑性模型B1. Set the viscoelastic plastic model of the callus area
利用宾汉-麦克斯韦粘弹塑性模型建立骨痂区域的粘弹性生物力学模型,该粘弹塑性模型由线性弹簧、牛顿粘壶和一个摩擦件组成。通过建立皮质骨和骨痂的生物力学模型,编写UMAT子程序,计算骨痂区域的粘弹塑性行为。A viscoelastic biomechanical model of the callus region was established using the Bingham-Maxwell viscoelastic plastic model, which consisted of a linear spring, a Newtonian stick pot and a friction element. By establishing the biomechanical model of cortical bone and callus, UMAT subprogram was written to calculate the viscoelastic-plastic behavior of callus area.
B2、计算骨痂区域应变状态B2. Calculate the strain state of the callus area
在ABAQUS中进行粘弹塑性有限元分析得到有限元模型各单元应变随时间变化曲线。对于每个牵张时间周期,使用ndiff等距分割每个牵张时间周期的应变样本,按照每个样本最大峰值刺激进行采样,得到ndiff个用于组织分化算法的畸变应变γ0和膨胀应变ε0;Viscoelastic-plastic finite element analysis was performed in ABAQUS to obtain the strain curve of each element of the finite element model with time. For each stretch time period, use n diff to equally divide the strain samples for each stretch time period, and sample by the maximum peak stimulus for each sample to obtain n diff distortion strain γ 0 and dilation for the tissue differentiation algorithm strain ε 0 ;
式中,ε1,ε2,ε3分别为各单元的三个主应变。In the formula, ε 1 , ε 2 , and ε 3 are the three principal strains of each element, respectively.
进一步,所述A4骨再生动态过程模拟模块将B2有限元分析得到截骨区域有限元模型各单元的畸变应变γ0和膨胀应变ε0结果作为输入,运用模糊逻辑控制,确定应变状态在组织分化图上的位置,并输出组织类型变化的结果,更新组织材料类型,再现骨痂的骨再生过程,包括:Further, the A4 bone regeneration dynamic process simulation module takes the results of the distortion strain γ 0 and the expansion strain ε 0 of each element of the finite element model of the osteotomy area obtained from the B2 finite element analysis as input, and uses fuzzy logic control to determine the strain state in tissue differentiation. position on the map, and output the results of tissue type changes, update tissue material types, and reproduce the bone regeneration process of callus, including:
C1、建立组织分化模型C1. Establish a tissue differentiation model
将截骨区域有限元模型(即所有皮质骨和骨痂)中每个单元的七个变量作为输入,包括:单元中骨含量的百分比,单元中软骨含量的百分比,单元的膨胀应变,单元的畸变应变,单元的血管分布,邻近单元中骨含量的影响和邻近单元血供的影响。建立包含血管生成、膜内骨化、软骨生成、软骨内骨化、组织破坏、骨成熟和骨吸收的模糊规则,用于描述在力学刺激作用下组织分化结果,最终输出每个单元的骨,软骨和血管的含量变化的百分比。Seven variables for each element in the finite element model of the osteotomy area (i.e. all cortical bone and callus) were used as inputs, including: the percentage of bone content in the element, the percentage of cartilage content in the element, the expansion strain of the element, the Distortion strain, vascularity of cells, effect of bone content in adjacent cells and effect of blood supply to adjacent cells. Establish fuzzy rules including angiogenesis, intramembranous ossification, chondrogenesis, endochondral ossification, tissue destruction, bone maturation and bone resorption to describe the results of tissue differentiation under mechanical stimulation, and finally output the bone of each unit, Percent change in cartilage and blood vessel content.
C2、更新材料属性C2. Update material properties
1)将步骤C1模糊逻辑控制输出的模糊值经过去模糊化得到输出变量的改变量,从而得到组织分化的各单元中血供、骨和软骨含量的改变量ΔCi:1) Defuzzify the fuzzy value output by the fuzzy logic control of step C1 to obtain the change amount of the output variable, thereby obtaining the change amount ΔC i of blood supply, bone and cartilage content in each unit of tissue differentiation:
式中Cperf为各单元中血供含量,Cbone为各单元中骨含量,Ccart为各单元中软骨含量;where C perf is the blood supply content in each unit, C bone is the bone content in each unit, and C cart is the cartilage content in each unit;
Cbone=Clamellar+Cwoven C bone =C lamellar +C woven
式中,Clamellar为各单元中板层骨含量,Cwoven为各单元中编织骨含量;In the formula, C lamellar is the lamellar bone content in each unit, and C woven is the woven bone content in each unit;
Ci+1=ΔCiΔt+Ci C i+1 =ΔC i Δt+C i
上式为迭代函数,Ci+1为当前时间单元中对应的血供、骨或软骨含量,Ci为前一时间单元中对应的血供、骨和软骨含量,Δt为时间步长。The above formula is an iterative function, C i+1 is the corresponding blood supply, bone or cartilage content in the current time unit, C i is the corresponding blood supply, bone and cartilage content in the previous time unit, Δt is the time step.
在每次更新组织含量运行结束时,需要逐步地将截骨区域有限元模型(即所有皮质骨和骨痂)各单元血供、骨和软骨含量Ci重新规范化:对于皮质骨区域各单元血供、骨和软骨含量保持初始状态不变,则对应的皮质骨杨氏模量、泊松比不变;对于骨痂区域各单元血供、骨和软骨含量进行更新并使其范围0≤Ci≤1;At the end of each update tissue content run, it is necessary to gradually renormalize the blood supply, bone and cartilage content C i of each unit of the finite element model of the osteotomy area (i.e. all cortical bone and callus): for each unit of blood in the cortical bone area If the contents of blood supply, bone and cartilage remain unchanged at the initial state, the corresponding Young's modulus and Poisson's ratio of cortical bone remain unchanged; the blood supply, bone and cartilage contents of each unit in the callus area are updated and the range is 0≤C i ≤ 1;
2)在整个牵张步骤的过程中调用ndiff次模糊逻辑控制器来计算各单元血供、骨和软骨含量Ci的变化;2) in the process of the whole stretch step, call the fuzzy logic controller n diff times to calculate the changes of blood supply, bone and cartilage content C i of each unit;
3)之后根据骨痂区域各单元中骨、软骨和结缔组织的含量,对骨痂区域每个单元的材料属性进行更新;3) Then update the material properties of each unit in the callus area according to the content of bone, cartilage and connective tissue in each unit of the callus area;
其中:Ccoon=1-Cbone-Ccart Among them: C coon = 1-C bone -C cart
式中,Ccoon为各单元中结缔组织含量In the formula, C coon is the content of connective tissue in each unit
对于骨痂区域每个单元杨氏模量Eele的更新,使用:For the update of the Young's modulus E ele per cell in the callus area, use:
式中,Elamellar为板层骨杨氏模量,Ewoven为编织骨杨氏模量,Ecart为软骨杨氏模量,Ecoon为结缔组织杨氏模量,上述杨氏模量均由实验获得;In the formula, E lamellar is the Young's modulus of lamellar bone, E woven is the Young's modulus of woven bone, E cart is the Young's modulus of cartilage, and E coon is the Young's modulus of connective tissue, and the above-mentioned Young's modulus is determined by obtained experimentally;
对于骨痂区域每个单元泊松比υele的更新,使用:For the update of the Poisson's ratio υ ele per cell in the callus region, use:
υele=υlamellarClamellar+υwovenCwoven+υcartCcart+υcoonCcoon υ ele =υ lamellar C lamellar +υ woven C woven +υ cart C cart +υ coon C coon
式中,υlamellar为板层骨泊松比,υwoven为编织骨泊松比,υcart为软骨泊松比,υcoon为结缔组织泊松比,上述泊松比均由实验获得;In the formula, υ lamellar is the Poisson’s ratio of lamellar bone, υ woven is the Poisson’s ratio of woven bone, υ cart is the Poisson’s ratio of cartilage, and υ coon is the Poisson’s ratio of connective tissue, and the above Poisson’s ratios are obtained by experiments;
进一步,所述C1中初始骨、软骨和血供含量通过步骤A1获得,即若单元为皮质骨中的单元则采用皮质骨中单元对应的参数,若单元为骨痂中的单元则采用骨痂中单元对应的参数;相邻单元的影响是通过对每个有限元单元质心处进行采样,利用切比雪夫距离获得每个单元的相邻区域,之后通过高斯核函数判断相邻区域每个相邻单元对其影响的权重,最后通过加权平均判定相邻区域内的相邻单元的影响。Further, the initial bone, cartilage and blood supply contents in the C1 are obtained through step A1, that is, if the unit is a unit in the cortical bone, the parameters corresponding to the unit in the cortical bone are used, and if the unit is a unit in the callus, the callus is used. The parameters corresponding to the middle element; the influence of adjacent elements is to sample the centroid of each finite element element, use the Chebyshev distance to obtain the adjacent area of each element, and then use the Gaussian kernel function to determine each phase of the adjacent area. The weight of the influence of adjacent units on it, and finally the influence of adjacent units in the adjacent area is determined by weighted average.
进一步,所述C1中骨成熟和骨吸收规则并不是真正用模糊逻辑实现的,而是作为单独的后处理步骤来实现。这种分离是为了实现编织骨和板层骨的不同吸收率对成骨产生不同的影响,并且区别于组织破坏过程造成的骨含量减少。Further, the bone maturation and bone resorption rules in C1 are not really implemented with fuzzy logic, but as separate post-processing steps. This separation is to achieve that the different resorption rates of woven and lamellar bone have different effects on osteogenesis and are distinct from the reduction in bone content caused by the tissue destruction process.
进一步,所述牵张成骨的仿真系统,将A4骨再生动态过程模拟模块的输出结果作为输入,传回A3截骨区域计算生物力学分析模块,进入下一个分析步计算,直至牵张结束后骨痂处所有单元骨含量为100%,仿真结束并输出成骨结果。Further, the simulation system of distraction osteogenesis takes the output result of the A4 bone regeneration dynamic process simulation module as an input, and sends it back to the A3 osteotomy area calculation biomechanical analysis module, and enters the next analysis step calculation until the distraction ends. The bone content of all units at the callus is 100%, the simulation ends and the osteogenesis results are output.
进一步,所述牵张成骨的仿真系统,在迭代过程中还需要对上一个分析步骨痂区域由于牵张加载导致的大变形单元进行有限元网格重划分和状态数据映射包括:(1)将变形后的网格模型进行模型重塑,生成一个未划分网格的几何模型;(2)利用先前单元的网格尺寸将变形后新的几何模型进行网格划分,得到变形后新的无畸变网格;(3)每一个新的网格根据所在位置判断其与原有每个旧网格相交部分的体积,并计算相交部分的体积占当前网格的权重;(4)将旧网格的每个单元的当前状态按照其对应的加权和赋予到新网格的相应单元上。Further, in the simulation system of distraction osteogenesis, in the iterative process, it is also necessary to perform finite element mesh re-division and state data mapping on the large deformed element in the callus region of the previous analysis step due to distraction loading, including: (1 ) Reshape the deformed mesh model to generate an undivided geometric model; (2) Use the mesh size of the previous unit to mesh the new deformed geometric model to obtain a new deformed geometric model. Distortion-free grid; (3) Each new grid determines the volume of the intersecting part with each old grid according to its location, and calculates the weight of the volume of the intersecting part in the current grid; (4) Combine the old grid The current state of each cell of the grid is assigned to the corresponding cell of the new grid according to its corresponding weighted sum.
本发明提供的牵张成骨的仿真系统中,所述牵张成骨的仿真系统依据牵张成骨实施过程中,施加不同的牵张条件会引起骨痂区域组织不同的成骨效应;通过对牵张成骨的骨再生过程进行仿真计算,根据输出的成骨结果判定最佳的牵张加载模式;另外,本发明在牵张参数设置模块提供针对患者的个性化参数设置包括:牵张期牵张速率、牵张期牵张频率、牵张期持续时间、巩固期施加牵-压耦合刺激时期、牵-压耦合载荷施加速率、牵压耦合载荷施加频率和牵张器刚度;用户可以自定义牵张参数,方便医生寻找针对患者的最佳力学刺激条件,有助于缩短整个治疗时间,进而降低并发症的发生率。In the simulation system for distraction osteogenesis provided by the present invention, the simulation system for distraction osteogenesis is based on the fact that different distraction conditions will cause different osteogenic effects in the callus area during the implementation of distraction osteogenesis; The bone regeneration process of distraction osteogenesis is simulated and calculated, and the best distraction loading mode is determined according to the output osteogenesis results; in addition, the present invention provides personalized parameter settings for patients in the distraction parameter setting module, including: distraction period stretch rate, stretch period stretch frequency, stretch period duration, stretch-compression coupled stimulus period applied during consolidation period, stretch-compression coupled load application rate, stretch-compression coupled load application frequency, and stretcher stiffness; user can Customized stretch parameters make it easier for doctors to find the best mechanical stimulation conditions for the patient, which can help shorten the entire treatment time, thereby reducing the incidence of complications.
此外,本发明的牵张成骨的仿真系统软件采用模块化结构,仿真程序具有良好的可扩展性,操作运行方便,利用模糊逻辑实现基于应变调控的组织分化进行数值分析,提高了系统设计的效率和准确性,也可用于其它类似的骨再生系统设计。In addition, the simulation system software of distraction osteogenesis of the present invention adopts a modular structure, the simulation program has good scalability, and the operation is convenient, and the fuzzy logic is used to realize the numerical analysis of tissue differentiation based on strain regulation, which improves the system design. The efficiency and accuracy can also be used in other similar bone regeneration system designs.
附图说明:Description of drawings:
图1是本发明牵张成骨的仿真系统的示意图;Fig. 1 is the schematic diagram of the simulation system of distraction osteogenesis of the present invention;
图2是本发明牵张成骨的仿真系统实施的流程图;Fig. 2 is the flow chart of the simulation system implementation of distraction osteogenesis of the present invention;
图3是本发明建立的一个模糊规则示意图Fig. 3 is a schematic diagram of a fuzzy rule established by the present invention
具体实施方式:Detailed ways:
以下将结合附图和具体实施例对本发明提出的一种牵张成骨的仿真系统作进一步详细说明。A simulation system for distraction osteogenesis proposed by the present invention will be described in further detail below with reference to the accompanying drawings and specific embodiments.
实施例1Example 1
本实施例提供一种牵张成骨的仿真系统,所述牵张成骨的仿真系统依据牵张成骨实施过程中,施加不同的牵张条件会引起骨痂区域组织不同的成骨效应;通过对牵张成骨的骨再生过程进行仿真计算,根据输出的成骨结果判定最佳的牵张加载模式;如图1所示,所述牵张成骨的仿真系统包括A1对象截骨区域个体化三维重建模块、A2牵张参数设置模块、A3截骨区域计算生物力学分析模块、A4骨再生动态过程模拟模块和A5显示模块。A1所述系统对象截骨区域个体化三维重建模块用于对对象截骨区域的CT图像进行自动分割并进行三维重建,得到对象截骨区域的个体化三维几何模型,然后进行网格划分处理;A2所述系统牵张参数设置模块用于对对象个体化三维截骨区域有限元模型设置不同的力学加载模式,作为A3截骨区域计算生物力学分析模块的输入;A3所述系统截骨区域计算生物力学分析模块用于依据A2牵张参数设置模块传入的加载参数,设置边界条件和材料属性。设置材料属性包括:在ABAQUS的用户材料设置皮质骨杨氏模量、泊松比和骨痂杨氏模量、泊松比、屈服应力、粘度系数(通过包含粘弹塑性生物力学模型的UMAT子程序进行定义材料类型),骨痂区域初始阶段被假定充满结缔组织,进行模拟牵张确定骨痂区域的力学刺激状态;A4所述系统骨再生动态过程模拟模块用于将有限元分析得到的应变结果作为输入,运用模糊逻辑控制,确定应变状态在组织分化图上的位置,并输出组织类型变化的结果,更新组织材料类型,再现骨痂的骨再生过程;A5所述系统显示模块用于显示所述牵张成骨仿真系统的计算结果。The present embodiment provides a simulation system for distraction osteogenesis, and the simulation system for distraction osteogenesis may cause different osteogenic effects of callus area tissue by applying different distraction conditions during the implementation of distraction osteogenesis; By simulating the bone regeneration process of distraction osteogenesis, the optimal distraction loading mode is determined according to the output osteogenesis results; as shown in Figure 1, the simulation system of distraction osteogenesis includes the osteotomy area of the A1 object Individualized 3D reconstruction module, A2 distraction parameter setting module, A3 osteotomy area computational biomechanical analysis module, A4 bone regeneration dynamic process simulation module and A5 display module. The system object osteotomy region individualized 3D reconstruction module described in A1 is used to automatically segment and perform 3D reconstruction of the CT image of the object osteotomy region, obtain an individualized 3D geometric model of the object osteotomy region, and then perform grid division processing; The system distraction parameter setting module in A2 is used to set different mechanical loading modes for the individualized three-dimensional osteotomy area finite element model of the object, which is used as the input of the biomechanical analysis module for calculating the osteotomy area in A3; the system osteotomy area calculation in A3 The biomechanical analysis module is used to set the loading parameters input from the module according to the A2 stretch parameters, and to set the boundary conditions and material properties. Setting the material properties includes: setting the Young's modulus of cortical bone, Poisson's ratio and Young's modulus of callus, Poisson's ratio, yield stress, viscosity coefficient (via the UMAT subsection containing the viscoelastic-plastic biomechanical model) in ABAQUS's User Materials The program defines the material type), the initial stage of the callus area is assumed to be filled with connective tissue, and simulated distraction is performed to determine the mechanical stimulation state of the callus area; the dynamic process simulation module of the system described in A4 is used to simulate the strain obtained by the finite element analysis. The result is used as input, and fuzzy logic control is used to determine the position of the strain state on the tissue differentiation map, and output the result of tissue type change, update the tissue material type, and reproduce the bone regeneration process of the callus; the system display module described in A5 is used to display The calculation results of the distraction osteogenesis simulation system.
如图1~2所示,在所述的牵张成骨仿真系统中,所述A2牵张参数设置模块设置所需参数包括:牵张期牵张速率、牵张期牵张频率、牵张期持续时间、巩固期施加牵-压耦合刺激时期、牵-压耦合载荷施加速率、牵压耦合载荷施加频率和牵张器刚度;此外,在所述系统迭代过程中需要将A4骨再生动态过程模拟模块的输出结果作为输入,传回A3截骨区域计算生物力学分析模块,进入下一个分析步计算,直至牵张结束后骨痂处所有单元骨含量为100%,仿真结束并输出成骨结果。此外,在迭代过程中还需要对上一个分析步骨痂区域由于牵张加载导致的大变形单元进行有限元网格重划分和状态数据映射包括:(1)将变形后的网格模型进行模型重塑,生成一个未划分网格的几何模型;(2)利用先前单元的网格尺寸将变形后新的几何模型进行网格划分,得到变形后新的无畸变网格;(3)每一个新的网格根据所在位置判断其与原有每个旧网格相交部分的体积,并计算相交部分的体积占当前网格的权重;(4)将旧网格的每个单元的当前状态按照其对应的加权和赋予到新网格的相应单元上。As shown in Figures 1-2, in the described distraction osteogenesis simulation system, the required parameters set by the A2 distraction parameter setting module include: distraction rate, distraction frequency, distraction period duration, period of application of distraction-compression coupled stimulation during consolidation phase, rate of distraction-compression coupled load application, frequency of distraction-compression coupled load application, and distractor stiffness; in addition, the A4 bone regeneration dynamic process needs to be The output result of the simulation module is used as input, which is returned to the A3 osteotomy area calculation biomechanical analysis module, and the next analysis step is calculated until the bone content of all units at the callus after the distraction is 100%, and the simulation ends and the osteogenesis result is output. . In addition, in the iterative process, it is also necessary to perform finite element mesh re-division and state data mapping for the large-deformed elements in the callus region of the previous analysis step due to distraction loading, including: (1) The deformed mesh model is modeled Reshape to generate an ungridded geometric model; (2) use the mesh size of the previous element to mesh the deformed new geometric model to obtain a new deformed undistorted mesh; (3) each The new grid judges the volume of the intersecting part with each old grid according to its location, and calculates the weight of the volume of the intersecting part in the current grid; (4) Calculate the current state of each unit of the old grid according to its The corresponding weighted sums are assigned to the corresponding cells of the new grid.
具体的,在所述的牵张成骨仿真系统中,A1对象截骨区域个体化三维重建模块用于进行CT扫描,获取对象截骨区域的CT图像,对CT图像自动分割出对象的截骨区域,并进行三维重建和网格划分,得到对象截骨区域个体化的几何和有限元模型。模型由两部分组成:皮质骨和骨痂。对截骨区域有限元模型进行初始状态设置。初始状态设置包括初始皮质骨骨含量为100%、软骨含量为0%和血供为100%,初始骨痂区域骨含量为0%、软骨含量为0%和血供为0%,并将其保存在Excel文件中。Specifically, in the described distraction osteogenesis simulation system, the individualized 3D reconstruction module of the osteotomy area of the A1 object is used to perform CT scanning, obtain the CT image of the osteotomy area of the object, and automatically segment the CT image into the osteotomy of the object 3D reconstruction and meshing are performed to obtain the individualized geometric and finite element model of the osteotomy area of the object. The model consists of two parts: cortical bone and callus. Set the initial state of the finite element model of the osteotomy area. The initial state settings include the initial cortical bone content of 100%, the cartilage content of 0% and the blood supply of 100%, the initial callus region of 0% of bone content, 0% of cartilage content and 0% of blood supply. Saved in an Excel file.
具体的,在所述的牵张成骨仿真系统中,A3截骨区域计算生物力学分析模块依据A2牵张参数设置模块传入的加载参数,,设置边界条件和材料属性。设置材料属性包括:在ABAQUS的用户材料设置皮质骨杨氏模量、泊松比和骨痂杨氏模量、泊松比、屈服应力、粘度系数(通过包含粘弹塑性生物力学模型的UMAT子程序进行定义材料类型),骨痂区域初始阶段被假定充满结缔组织;Specifically, in the described distraction osteogenesis simulation system, the A3 osteotomy area computational biomechanical analysis module sets the boundary conditions and material properties according to the loading parameters input from the A2 distraction parameter setting module. Setting the material properties includes: setting the Young's modulus of cortical bone, Poisson's ratio and Young's modulus of callus, Poisson's ratio, yield stress, viscosity coefficient (via the UMAT subsection containing the viscoelastic-plastic biomechanical model) in ABAQUS's User Materials procedure to define the material type), the callus area is assumed to be filled with connective tissue at the initial stage;
B1、设置皮质骨的线弹性生物力学模型:B1. Set the linear elastic biomechanical model of cortical bone:
σs=Esεs (1)σ s =E s ε s (1)
式中,σs为线弹性模型应力,Es为线弹性模型弹性模量,εs为线弹性模型应变;where σ s is the linear elastic model stress, E s is the linear elastic model elastic modulus, ε s is the linear elastic model strain;
和骨痂区域的粘弹性生物力学模型(宾汉-麦克斯韦粘弹塑性模型):and a viscoelastic biomechanical model of the callus region (Bingham-Maxwell viscoelastic plastic model):
其中in
式中,σ为粘弹塑性模型应力,η为粘度系数,Ef为粘弹塑性模型弹性模量,σyield为粘弹塑性模型临界应力,ε为粘弹塑性模型应变,t为时间。where σ is the stress of the viscoelastic-plastic model, η is the viscosity coefficient, E f is the elastic modulus of the visco-elastic-plastic model, σ yield is the critical stress of the visco-elastic-plastic model, ε is the strain of the visco-elastic-plastic model, and t is the time.
将上述得到的(1)和(2)本构方程输入到ABAQUS的UMAT子程序中,模拟牵张获得骨痂区域的力学刺激应变状态;Input the above-obtained constitutive equations (1) and (2) into the UMAT subroutine of ABAQUS, and simulate the distraction to obtain the mechanically stimulated strain state of the callus area;
B2、应变结果数据的整理,包括:B2. Arrangement of strain result data, including:
在ABAQUS中进行粘弹性有限元分析得到有限元模型各单元应变随时间变化曲线。对于每个牵张周期,使用ndiff等距应变样本按照每个样本最大峰值刺激进行采样,得到ndiff个用于组织分化算法的应变分量。Viscoelastic finite element analysis was performed in ABAQUS to obtain the strain curve of each element of the finite element model with time. For each stretch cycle, n diff equidistant strain samples were used to sample the maximum peak stimulus per sample, resulting in n diff strain components for the tissue differentiation algorithm.
其中对于每个单元应变分量有:where for each element strain component is:
式中[ε]为单元主应变,ε11、ε22、ε33、ε12、ε23、ε13为ABAQUS求得的6个应变分量;where [ε] is the principal strain of the element, and ε 11 , ε 22 , ε 33 , ε 12 , ε 23 , and ε 13 are the six strain components obtained by ABAQUS;
通过上述方程的求解得到有限元模型各单元的三个主应变:The three principal strains of each element of the finite element model are obtained by solving the above equations:
式中,ε1,ε2,ε3分别为各单元的三个主应变;where ε 1 , ε 2 , and ε 3 are the three principal strains of each element, respectively;
由主应变可得到有限元模型各单元的畸变应变:The distortion strain of each element of the finite element model can be obtained from the principal strain:
式中,γ0为有限元模型各单元所受到的畸变应变;In the formula, γ 0 is the distortion strain received by each element of the finite element model;
由主应变可得到有限元模型各单元的膨胀应变:The expansion strain of each element of the finite element model can be obtained from the principal strain:
式中,ε0为有限元模型各单元所受到的膨胀应变。In the formula, ε 0 is the expansion strain experienced by each element of the finite element model.
具体的,在所述的牵张成骨仿真系统中,A4骨再生动态过程模拟模块;运用模糊逻辑控制,确定应变状态在组织分化图上的位置,并输出组织类型变化的结果,更新组织材料类型,再现骨痂的骨再生过程。包括:Specifically, in the described distraction osteogenesis simulation system, the A4 dynamic process simulation module of bone regeneration uses fuzzy logic control to determine the position of the strain state on the tissue differentiation map, output the results of tissue type changes, and update tissue materials type that reproduces the bone regeneration process of callus. include:
C1、建立组织分化模型C1. Establish a tissue differentiation model
1)、建立输入变量隶属度函数;1), establish the input variable membership function;
将截骨区域有限元模型(即所有皮质骨和骨痂)中每个单元的七个变量作为输入,包括:单元中骨含量的百分比、单元中软骨含量的百分比、单元的膨胀应变、单元的畸变应变、单元的血供、相邻单元中骨含量的百分比和相邻单元血供。其中,初始骨、软骨和血供含量通过步骤A1获得,即若单元为皮质骨中的单元则采用皮质骨中单元对应的参数,若单元为骨痂中的单元则采用骨痂中单元对应的参数;相邻单元的影响通过对每个有限元单元质心处进行采样,利用切比雪夫距离获得每个单元的相邻区域,再通过高斯核函数判断相邻区域每个相邻单元对其影响的权重,最后通过加权平均判定相邻区域内相邻单元的影响。Seven variables for each element in the finite element model of the osteotomy area (i.e. all cortical bone and callus) were used as inputs, including: the percentage of bone content in the element, the percentage of cartilage content in the element, the expansion strain of the element, the Distortion strain, blood supply to cells, percentage of bone content in adjacent cells, and blood supply to adjacent cells. Among them, the initial bone, cartilage and blood supply contents are obtained through step A1, that is, if the unit is a unit in the cortical bone, the parameters corresponding to the unit in the cortical bone are used, and if the unit is a unit in the callus, the parameter corresponding to the unit in the callus is used. Parameter; the influence of adjacent units is obtained by sampling the centroid of each finite element unit, using the Chebyshev distance to obtain the adjacent area of each unit, and then judging the influence of each adjacent unit in the adjacent area by the Gaussian kernel function. Finally, the influence of adjacent units in adjacent areas is determined by weighted average.
2)、建立模糊控制规则2), establish fuzzy control rules
建立描述在力学刺激(畸变应变和膨胀应变)下血管生成、膜内骨化、软骨生成、软骨内骨化和组织破坏等组织分化的模糊控制规则(如建立由17条if-then语言组成的模糊控制规则),如果存在或符合规则条件,则发生相对应的组织分化,这些规则描述了在力学刺激(畸变应变和膨胀应变)下的血管生成、膜内骨化、软骨生成、软骨内骨化和组织破坏的过程。Establish fuzzy control rules that describe tissue differentiation such as angiogenesis, intramembranous ossification, chondrogenesis, endochondral ossification and tissue destruction under mechanical stimulation (distortion strain and expansion strain) (such as establishing a 17 if-then language Fuzzy control rules), corresponding tissue differentiation occurs if the conditions of rules are present or are met, these rules describe angiogenesis, intramembranous ossification, chondrogenesis, endochondral bone under mechanical stimuli (distortion strain and expansion strain) process of transformation and tissue destruction.
如模糊控制器由17条语言的if-then规则组成(见图3),如果存在上述中if条件,则发生相对应的组织分化。这些规则描述了在力学刺激(畸变应变和膨胀应变)下的血管生成、膜内骨化、软骨生成、软骨内骨化和组织破坏的过程。For example, the fuzzy controller consists of 17 language if-then rules (see Figure 3). If the above-mentioned if-then conditions exist, the corresponding tissue differentiation will occur. These rules describe the processes of angiogenesis, intramembranous ossification, chondrogenesis, endochondral ossification and tissue destruction under mechanical stimuli (distorting and distending strain).
规则1至3代表了在力学刺激和相邻区域血供影响下的血管生成。当有中等应变和不低的相邻区域血供存在时,血供增加。
规则4至5描述了膜内骨化。如果相邻区域单元骨浓度不低时,则低力学刺激和足够血供的区域的骨浓度会增加。
规则6至8描述了软骨形成。发生在高力学刺激下,并且不受血供的影响。
规则9至12代表软骨钙化。需要有较高的软骨浓度,并且受到相邻骨浓度的影响。在血供充足和力学刺激相对较高的情况下发生。
规则13至14代表软骨内骨化。发生在中或高血供下。
规则15至17模拟了力学刺激过载导致的组织破坏。
此外,在模糊逻辑中添加了一个附加的规则,用于描述骨成熟和骨吸收的过程。Furthermore, an additional rule was added in fuzzy logic to describe the process of bone maturation and bone resorption.
3)、建立输出变量隶属度函数;3), establish the output variable membership function;
经过模糊规则描述的组织分化过程,最终输出各单元血供改变量、各单元骨含量改变量和各单元软骨含量改变量。After the tissue differentiation process described by fuzzy rules, the change of blood supply in each unit, the change in bone content in each unit and the change in cartilage content in each unit are finally output.
C2、更新材料属性C2. Update material properties
1)将步骤C1模糊逻辑控制输出的模糊值经过去模糊化得到输出变量的改变量,从而得到组织分化的各单元中血供、骨和软骨含量的改变量ΔCi:1) Defuzzify the fuzzy value output by the fuzzy logic control of step C1 to obtain the change amount of the output variable, thereby obtaining the change amount ΔC i of blood supply, bone and cartilage content in each unit of tissue differentiation:
式中Cperf为各单元中血供含量,Cbone为各单元中骨含量,Ccart为各单元中软骨含量;where C perf is the blood supply content in each unit, C bone is the bone content in each unit, and C cart is the cartilage content in each unit;
Cbone=Clamellar+Cwoven (9)C bone =C lamellar +C woven (9)
式中,Clamellar为各单元中板层骨含量,Cwoven为各单元中编织骨含量;In the formula, C lamellar is the lamellar bone content in each unit, and C woven is the woven bone content in each unit;
Ci+1=ΔCiΔt+Ci (10)C i+1 =ΔC i Δt+C i (10)
上式为迭代函数,Ci+1为当前时间单元中对应的血供、骨或软骨含量,Ci为前一时间单元中对应的血供、骨和软骨含量,Δt为时间步长。The above formula is an iterative function, C i+1 is the corresponding blood supply, bone or cartilage content in the current time unit, C i is the corresponding blood supply, bone and cartilage content in the previous time unit, Δt is the time step.
在每次更新组织含量运行结束时,需要逐步地将截骨区域有限元模型(即所有皮质骨和骨痂)各单元血供、骨和软骨含量Ci重新规范化:对于皮质骨区域各单元血供、骨和软骨含量保持初始状态不变,皮质骨杨氏模量、泊松比也不变;对于骨痂区域各单元血供、骨和软骨含量进行更新并使其范围0≤Ci≤1;At the end of each update tissue content run, it is necessary to gradually renormalize the blood supply, bone and cartilage content C i of each unit of the finite element model of the osteotomy area (i.e. all cortical bone and callus): for each unit of blood in the cortical bone area The contents of blood supply, bone and cartilage remain unchanged in the initial state, and the Young's modulus and Poisson's ratio of cortical bone also remain unchanged; the blood supply, bone and cartilage contents of each unit in the callus area are updated and set to the range 0≤C i ≤ 1;
2)在整个牵张步骤的过程中调用ndiff次模糊逻辑控制器来计算各单元血供、骨和软骨含量Ci的变化;2) in the process of the whole stretch step, call the fuzzy logic controller n diff times to calculate the changes of blood supply, bone and cartilage content C i of each unit;
3)之后根据骨痂区域各单元中骨、软骨和结缔组织的含量,对骨痂区域每个单元的材料属性进行更新;3) Then update the material properties of each unit in the callus area according to the content of bone, cartilage and connective tissue in each unit of the callus area;
其中:Ccoon=1-Cbone-Ccart (11)Where: C coon = 1-C bone -C cart (11)
式中,Ccoon为各单元中结缔组织含量In the formula, C coon is the content of connective tissue in each unit
对于骨痂区域每个单元杨氏模量Eele的更新,使用:For the update of the Young's modulus E ele per cell in the callus area, use:
式中,Elamellar为板层骨杨氏模量,Ewoven为编织骨杨氏模量,Ecart为软骨杨氏模量,Ecoon为结缔组织杨氏模量,上述杨氏模量均由实验获得;In the formula, E lamellar is the Young's modulus of lamellar bone, E woven is the Young's modulus of woven bone, E cart is the Young's modulus of cartilage, and E coon is the Young's modulus of connective tissue, and the above-mentioned Young's modulus is determined by obtained experimentally;
对于骨痂区域每个单元泊松比υele的更新,使用:For the update of the Poisson's ratio υ ele per cell in the callus region, use:
vele=vlamellarClamellar+vwovenCwoven+vcartCcart+vcoonCcoon (13)v ele =v lamellar C lamellar +v woven C woven +v cart C cart +v coon C coon (13)
式中,vlamellar为板层骨泊松比,vwoven为编织骨泊松比,vcart为软骨泊松比,υcoon为结缔组织泊松比,上述泊松比均由实验获得;In the formula, v lamellar is the Poisson's ratio of lamellar bone, v woven is the Poisson's ratio of woven bone, v cart is the Poisson's ratio of cartilage, and υ coon is the Poisson's ratio of connective tissue, and the above Poisson's ratios are obtained by experiments;
最终通过比较各组合参数加载的仿真计算中成骨结果,判定最佳的牵张加载模式。Finally, the optimal distraction loading mode was determined by comparing the osteogenesis results in the simulation calculation of loading with each combination of parameters.
本发明提供的牵张成骨的仿真系统中,所述牵张成骨的仿真系统依据牵张成骨实施过程中,施加不同的牵张条件会引起骨痂区域组织不同的成骨效应;通过对牵张成骨的骨再生过程进行仿真计算,根据输出的成骨结果判定最佳的牵张加载模式;另外,本发明在牵张参数设置模块提供针对患者的个性化参数设置包括:牵张期牵张速率、牵张期牵张频率、牵张期持续时间、巩固期施加牵-压耦合刺激时期、牵-压耦合载荷施加速率、牵压耦合载荷施加频率和牵张器刚度;用户可以自定义牵张参数,方便医生寻找针对患者的最佳力学刺激条件,有助于缩短整个治疗时间,进而降低并发症的发生率。In the simulation system for distraction osteogenesis provided by the present invention, the simulation system for distraction osteogenesis is based on the fact that different distraction conditions will cause different osteogenic effects in the callus area during the implementation of distraction osteogenesis; The bone regeneration process of distraction osteogenesis is simulated and calculated, and the best distraction loading mode is determined according to the output osteogenesis results; in addition, the present invention provides personalized parameter settings for patients in the distraction parameter setting module, including: distraction period stretch rate, stretch period stretch frequency, stretch period duration, stretch-compression coupled stimulus period applied during consolidation period, stretch-compression coupled load application rate, stretch-compression coupled load application frequency, and stretcher stiffness; user can Customized stretch parameters make it easier for doctors to find the best mechanical stimulation conditions for the patient, which can help shorten the entire treatment time, thereby reducing the incidence of complications.
另外,本发明的牵张成骨的仿真系统软件采用模块化结构,仿真程序具有良好的可扩展性,操作运行方便,利用模糊逻辑实现基于应变调控的组织分化进行数值分析,提高了系统设计的效率和准确性,也可用于其它类似的骨再生系统设计。In addition, the simulation system software of distraction osteogenesis of the present invention adopts a modular structure, and the simulation program has good scalability, convenient operation and operation, and uses fuzzy logic to realize the numerical analysis of tissue differentiation based on strain regulation, which improves the system design. The efficiency and accuracy can also be used in other similar bone regeneration system designs.
综上,上述实施例对牵张成骨的仿真系统的实施构型进行了详细说明,当然,本发明包括但不局限于上述实施中所列举的构型,任何在上述实施例提供的构型基础上进行变化的内容,均属于本发明所保护的范围。本领域人员可以根据上述实施例的内容举一反三。To sum up, the above embodiments describe in detail the implementation configuration of the simulation system for distraction osteogenesis. Of course, the present invention includes but is not limited to the configurations listed in the above embodiments, any configuration provided in the above embodiments Changes made on the basis belong to the scope of protection of the present invention. Those skilled in the art can draw inferences from the contents of the foregoing embodiments.
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