Nov 29, 2011 - hip joints the spherical femoral head articulates in a hemispherical UHMWPE socket. Use a polymer on metal couple so as to achieve low friction and low contact pressure. Now we know the polymer has an ultimate tensile strength of appro
and the types of arthroplasty performed are shown in Tables. II and ... arthroplasties performed. Number of ..... in all 12 a Girdlestone arthroplasty was performed.
Gonzalez Della Valle A, Serota A, Go G, Sorriaux G, Sculco TP, Sharrock NE, et al. Venous thromboembolism .... Yu HT, Dylan ML, Lin J, Dubois RW. Hospitals' ...
Abstract: Instability after total hip arthroplasty (THA) is not a rare occurrence. Numerous factors have been associated with dislocation including surgical approach, implant design, failure to restore proper hip mechanics and soft tissue restraints,
V early osteointegration. On-growth of bone to porous coated prostheses is ... rich femoral component or with the ce- ... total hip arthroplasty in dogs (1, 2). Loo-.
Radiological analysis assessing heterotopic ossification, femoral osteolysis and femoral stem ... following total joint replacement.12 A retrospec- tive study by ...
Total hip replacement (THR) is a very common procedure undertaken in up to 285 000 .... diagnosis can include activity-related pain, aseptic loosening,.
an ideal total hip replacement with a large femoral head and a high head-neck ratio. B: Cam-type impingement in the native hip caused by a reduced femoral head-neck offset and similar impingement in a prosthetic hip with a small femoral head and a sk
575. INTRODUCTION. Total hip replacement (THR) provides a very effective ... arthroplasty, bilateral arthroplasty; those transferred or initially treated at other ...
90% (Schulte et al 1993; Neumann, Freund and SÃËrenson. 1994). Since its ..... Fowler JL, Gie GA, Lee AJC, Ling RSM. .... Clin On/top l993;292: 191-201. VOL.
Department of Trauma and Orthopaedic Surgery, Medical School, Uni- versity of Newcastle upon Tyne, Newcastle upon Tyne ... age orthopaedic surgeon in a non-specialist hospital is not known. The published data from the Norwegian and ..... 1. Medical D
Despite the current success of total hip replacement, we continue to strive for improvements, particularly in the durability or survivorship of the components,.
Total hip replacement (THR) may be required for patients with a high dislocated hip as a con- sequence of severe developmental dysplasia of the hip (DDH),1 ...
May 30, 2016 - introduction: In the Middle East, severe developmental dysplasia of the hip with subsequent high dislocation is often seen. We assessed the ...
stable (greater than the control) when walking over barriers as was roll for the sit-to-stand task, indicative of ... after total hip replacement regarding the risk of a fall, especially in the elderly. Most patients ... metre cable to a computer whi
flap, following damage to the inferior branch of the superior gluteal nerve, or by failure ... flap, was used in 29 hips, and the posterior. (P) .... was undisplaced.
resulting in deformities, protrusio acetabuli and malalignment of the limbs. Ligamentous laxity is seen frequently. In the past few decades there has been an ...
primary total hip replacements and 11 were revision operations, with aseptic loosening of the original implant being the main indication for revision. The.
D. W. MURRAY, A. R. BRITTON, C. J. K. BULSTRODE. From the Nuffield Orthopaedic Centre, Oxford, England. The recommendation that patients having a total hip replacement should receive pharmacological thromboprophylaxis is based on the belief that fata
ossification is seen in 5 per cent of hips not previously operated on. Harris noted myositis ossificans in. 14 per cent of patients following total hip replacement.
Arthritis of the hip joint occurs when the joint cartilage wears out. This results in pain, stiffness, and frequently a limp. The pain is usually located in the groin or ...
Now that total hip replacement (THR) is widely used and accepted ... made on the long-term results of Charnley arthroplasty in .... Revision of Girdlestone. 1.
Marc E. Umlas. From the Centre for Total Joint Replacement, New York, USA. We report 16 cases of erythematous eruption on the skin within the flaps of the ...
Artificial Total Hip Replacement
Learning Objectives After studying this case study, you should be able to do the following: 2. Name the four components found in the 1. List and briefly explain six biocompatibility artificial hip replacement, and, for each, list its considerations relative to materials that are specific material requirements. employed in artificial hip replacements.
hotograph showing the components of an artificial total hip
replacement (in exploded perspective). These components are (from left to right) as follows: femoral stem, ball, acetabular cup insert, and acetabular cup. (Photograph courtesy of Zimmer, Inc., Warsaw, IN, USA.)
ANATOMY OF THE HIP JOINT
As a prelude to discussing the artificial hip, let us first briefly address some of the anatomical features of joints in general and the hip joint in particular. The joint is an important component of the skeletal system. It is located at bone junctions, where loads may be transmitted from bone to bone by muscular action; this is normally accompanied by some relative motion of the component bones. Bone tissue is a complex natural composite consisting of soft and strong protein collagen and brittle hydroxyapatite, which has a density between 1.6 and 1.7 g/cm3. Bone is an anisotropic material with mechanical properties that differ in the longitudinal (axial) and transverse (radial) directions (Table CS4.1). The articulating (or connecting) surface of each joint is coated with cartilage, which consists of body fluids that lubricate and provide an interface with a very low coefficient of friction that facilitates the bone sliding movement.
Table CS4.1 Mechanical Characteristics of Human Long Bone, Both Parallel and Perpendicular to the Bone Axis Parallel to Bone Axis
Perpendicular to Bone Axis
17.4 (2.48 ⫻ 106)
11.7 (1.67 ⫻ 106)
Ultimate strength, tension, MPa (ksi)
Ultimate strength, compression, MPa (ksi)
Elongation at fracture
Property Elastic modulus, GPa (psi)
Source: From D. F. Gibbons, “Biomedical Materials,” pp. 253–254, Handbook of Engineering in Medicine and Biology, D. G. Fleming and B. N. Feinberg, CRC Press, Boca Raton, FL, 1976. With permission.
CS4.1 Anatomy of the Hip Joint • CS4.2 Figure CS4.1 Schematic diagram of human hip joints and adjacent skeletal components. Spine
The human hip joint (Figure CS4.1) occurs at the junction between the pelvis and the upper leg (thigh) bone, or femur. A relatively large range of rotary motion is permitted at the hip by a ball-and-socket type of joint; the top of the femur terminates in a ball-shaped head that fits into a cuplike cavity (the acetabulum) within the pelvis. An x-ray of a normal hip joint is shown in Figure CS4.2a. This joint is susceptible to fracture, which normally occurs at the narrow region just below the head. An x-ray of a fractured hip is shown in Figure CS4.2b; the arrows show the two ends of the fracture line through the femoral neck. Furthermore, the hip may become diseased (osteoarthritis); in such a case, small lumps of bone form on the rubbing surfaces of the joint, which causes pain as the head rotates in the acetabulum. Damaged and diseased hip joints have been replaced with artificial or prosthetic ones with moderate
Figure CS4.2 X-rays of (a) a normal hip joint and (b) a fractured hip joint. The arrows in (b) show the two ends of the fracture line through the femoral neck.
CS4.3 • Case Study 4
Artificial Total Hip Replacement
Acetabular cup Ball Fixation agent
Femoral stem Fixation agent
Femur ( a)
Figure CS4.3 (a) Schematic diagram and (b) x-ray of an artificial total hip replacement. success, beginning in the late 1950s. Total hip replacement surgery involves the removal of the head and the upper portion of the femur, as well as some of the bone marrow at the top of the remaining femur segment. Into this hole within the center of the femur a metal anchorage stem is secured that has the ball portion of the joint at its other end. In addition, the replacement cup socket must be attached to the pelvis. This is accomplished by removal of the old cup and its surrounding bone tissue. The new socket is affixed into this recess. A schematic diagram of the artificial hip joint is presented in Figure CS4.3a; Figure CS4.3b shows an x-ray of a total hip replacement. In the remainder of this case study, we discuss material constraints and materials that have been used with the greatest degree of success for the various artificial hip components.
MATERIAL REQUIREMENTS In essence, there are four basic components to the artificial hip: (1) the femoral stem, (2) the ball that attaches to this stem, (3) the acetabular cup that is affixed to the pelvis, and (4) a fixation agent that secures the stem into the femur and the cup to the pelvis. The property constraints on the materials to be used for these elements are stringent because of the chemical and mechanical complexity of the hip joint. Some of the requisite material characteristics will now be discussed. Whenever any foreign material is introduced into the body environment, rejection reactions occur. The magnitude of rejection may range from mild irritation or inflammation to death. Any implant material must be biocompatible; that is, it must produce a minimum degree of rejection. Products resulting from reactions with body fluids must be tolerated by the surrounding body tissues such that normal tissue function is unimpaired. Biocompatibility is a function of the location of the implant, as well as its chemistry and shape. Body fluids consist of an aerated and warm solution containing approximately 1 wt% NaCl in addition to other salts and organic compounds in relatively minor concentrations. Thus, body fluids are very corrosive, which for metal alloys can lead not only to uniform corrosion but also to crevice attack and pitting and, when stresses are present,
CS4.2 Material Requirements • CS4.4 to fretting,1 stress corrosion cracking, and corrosion fatigue. It has been estimated that the maximum tolerable corrosion rate for implant metal alloys is about 0.01 mil per year (2.5 ⫻ 10⫺4 mm per year). Another adverse consequence of corrosion is the generation of corrosion products that either are toxic or interfere with normal body functions. These substances are rapidly transported throughout the body; some may segregate in specific organs. Even though others may be excreted from the body, they may nevertheless persist in relatively high concentrations because of the ongoing corrosion process. The bones and replacement components within the hip joint must support forces that originate from outside the body, such as those due to gravity; in addition, they must transmit forces that result from muscular action such as walking. These forces are complex and fluctuate with time in magnitude, direction, and rate of application. Thus, mechanical characteristics such as modulus of elasticity, yield strength, tensile strength, fatigue strength, fracture toughness, and ductility are all important considerations relative to the materials of choice for the prosthetic hip. For example, the material used for the femoral stem should have minimum yield and tensile strengths of approximately 500 MPa (72,500 psi) and 650 MPa (95,000 psi), respectively, and a minimum ductility of about 8%EL. In addition, the fatigue strength [for bending stresses that are fully reversed (Figure 8.17a of Introduction; Figure 9.23a of Fundamentals)] should be at least 400 MPa (60,000 psi) at 107 cycles. For the average person, the load on the hip joint fluctuates on the order of 106 times per year. Ideally, the modulus of elasticity of the prosthetic material should match that of bone. A significant difference can lead to deterioration of the surrounding bone tissue and implant failure, which requires a second surgery and another prosthetic implant. Furthermore, because the ball-and-cup articulating surfaces rub against one another, wear of these surfaces is minimized by using very hard materials. Excessive and uneven wear can lead to a change in shape of the articulating surfaces and cause the prosthesis to malfunction. In addition, particulate debris will be generated as the articulating surfaces wear against one another; accumulation of this debris in the surrounding tissues can also lead to inflammation. Frictional forces at these rubbing counterfaces should also be minimized to prevent loosening of the femoral stem and acetabular cup assembly from their positions secured by the fixation agent. If these components do become loose over time, the hip joint will experience premature degradation that may require it to be replaced. Three final important material factors are density, property reproducibility, and cost. It is highly desirable that lightweight components be used, that material properties from prosthesis to prosthesis remain consistent over time, and, of course, that the cost of the prosthesis components be reasonable. Ideally, an artificial hip that has been surgically implanted should function satisfactorily for the life of the recipient and not require replacement. For current designs, lifetimes range between 15 and 25 years. Although this is a substantial improvement from the previous 5- to-10-year figures, longer lifetimes are still desirable. Several final comments are in order relative to biocompatibility assessment. Biocompatibility of materials is usually determined empirically; that is, tests are conducted wherein materials are implanted in laboratory animals and the biocompatibility of each material is judged on the basis of rejection reactions, level of corrosion, generation of toxic substances, and so on. This procedure is then repeated on humans for materials that were found to be relatively biocompatible in animals. It is difficult to predict the biocompatibility of a material. For example, mercury, when ingested into the 1
Fretting is a combination of corrosion and wear in which corrosion produces small debris (generally oxide particles) that increases the friction and induces greater abrasion.
CS4.5 • Case Study 4
Artificial Total Hip Replacement
body, is poisonous; however, dental amalgams, which have high mercury contents, have generally been found to be very biocompatible. Because of this biocompatibility assessment issue, most manufacturers select only materials that have been approved for biomedical use. One final requirement for implant materials is that they be nonmagnetic [i.e., do not exhibit ferromagnetic or ferrimagnetic behavior (Chapter 20 of Introduction; Chapter 18 of Fundamentals)]. A frequently used medical diagnostic tool is MRI (magnetic resonance imaging) spectroscopy, a medical test in which the patient is subjected to a very strong magnetic field. The presence of any ferromagnetic/ferrimagnetic materials implanted in the patient will disrupt the applied magnetic field and render MRI spectroscopy unusable. In addition, the magnitudes of these magnetic fields are such that significant forces may be brought to bear on any magnetic implant materials; these forces may loosen the implant and/or harm the patient. Ferromagnetic materials that should be avoided for implant applications include some ferrous alloys (i.e., ferritic and martensitic stainless steels) and alloys with high contents of nickel and/or cobalt.
MATERIALS EMPLOYED Femoral Stem and Ball Early prosthetic hip designs called for both the femoral stem and ball to be of the same material—a stainless steel. Subsequent improvements have been introduced, including the use of materials other than stainless steel and constructing the stem and ball from different materials. Indeed, stainless steel is rarely used in current implant designs. The opening photograph of this case study shows one hip replacement design. Currently, the femoral stem is constructed from a metal alloy of which there are two primary types: cobalt–chromium–molybdenum and titanium. Some models still use 316L stainless steel, which has a very low sulfur content (⬍ 0.002 wt%); its composition is given in Table 11.4 of Introduction (Table 13.4 of Fundamentals). The principal disadvantages of this alloy are its susceptibility to crevice corrosion and pitting and its relatively low fatigue strength. As a result, its use has decreased. Various Co–Cr–Mo alloys are used for artificial hip prostheses. One that has been found especially suitable, designated F75, is a cast alloy that has a composition of 66 wt% Co, 28 wt% Cr, and 6 wt% Mo. Its mechanical properties and corrosion rate range are listed in Table CS4.2. The corrosion and fatigue characteristics of this alloy are excellent.
Table CS4.2 Mechanical and Corrosion Characteristics of Three Metal Alloys That Are Commonly Used for the Femoral Stem Component of the Prosthetic Hip
CS4.3 Materials Employed • CS4.6 Of the metal alloys that are implanted for prosthetic hip joints, probably the most biocompatible is the titanium alloy extra low interstitial (ELI)2 Ti–6Al–4V; its composition is 90 wt% Ti, 6 wt% Al, and 4 wt% V. The optimal properties for this material are produced by hot forging; any subsequent deformation and/or heat treatment should be avoided to prevent the formation of microstructures that are deleterious to its bioperformance. The properties of this alloy are also listed in Table CS4.2. Recent improvements for this prosthetic device include using a ceramic material for the ball component rather than any of the aforementioned metal alloys. The ceramics of choice are a high-purity and polycrystalline aluminum oxide or zirconium oxide, which are harder and more wear resistant than metals and generate lower frictional stresses at the joint. However, the elastic moduli of these ceramics are large and the fracture toughness of alumina is relatively low. Hence, the femoral stem is still fabricated from one of the above alloys and is then attached to the ceramic ball; this femoral stem–ball component thus becomes a two-piece unit. The materials selected for use in an orthopedic implant come after years of research into the chemical and physical properties of a host of different candidate materials. Ideally, the material(s) of choice not only will be biocompatible but also will have mechanical properties that match the biomaterial being replaced—bone. However, no synthetic material is both biocompatible and possesses the property combination of bone and the natural hip joint—low modulus of elasticity, relatively high strength and fracture toughness, low coefficient of friction, and excellent wear resistance. Consequently, material property compromises and trade-offs must be made. For example, recall that the modulus of elasticity of bone and femoral stem materials should be closely matched such that accelerated deterioration of the bone tissue adjacent to the implant is avoided. Unfortunately, synthetic materials that are both biocompatible and relatively strong also have high moduli of elasticity. Thus, for this application, it was decided to trade off a low modulus for biocompatibility and strength.
Acetabular Cup Some acetabular cups are made from one of the biocompatible alloys or aluminum oxide. More commonly, however, lightly crosslinked ultra-high-molecular-weight polyethylene (Section 15.19 of Introduction; Section 13.16 of Fundamentals) is used. This material is virtually inert in the body environment and has excellent wear-resistance characteristics; furthermore, it has a very low coefficient of friction when in contact with the materials used for the ball component of the socket. Crosslinking the polyethylene significantly reduces the wear rate. A two-component cup assembly is shown for the total hip implant in the opening photograph for this case study. It consists of an ultra-high-molecular-weight polyethylene insert that fits within the cup; this cup is fabricated from one of the metal alloys listed in Table CS4.2, which, after implantation, becomes bonded to the pelvis.
Fixation Successful performance of the artificial hip joint calls for the secure attachment of both the femoral stem to the femur and the acetabular cup to the pelvis. Insecure attachment of either component ultimately leads to a loosening of that component and the accelerated degradation of the joint. Two fixation methods, cemented and noncemented,3 are commonly used to secure these two prosthetic components to their surrounding bone
The term “extra-low interstitial” means that the concentrations of interstitial impurities such as carbon, nitrogen, and oxygen are maintained at very low levels. Although the presence of these impurities increases strength (by solid-solution strengthening), ductility may be reduced significantly to unacceptable levels. 3 Noncemented fixation may also be referred to as uncemented, cementless, or slip-fit fixation.
CS4.7 • Case Study 4
Artificial Total Hip Replacement
structures. For cemented attachment, the most commonly used fixation agent is a poly(methyl methacrylate) (acrylic) bone cement while for noncemented attachment the stem and cup are coated with a porous surface layer and ingrowth of bone into the surface pores fixates the implant to the bone. Noncemented attachment is most commonly used in the United States. The porous layer commonly consists of either a sintered metal powder or an electrosprayed metal. Such a coating has been applied to the upper stem and acetabular cup regions of the hip replacement shown in the opening photograph for this case study. The growth of bone tissue into this three-dimensional pore network provides a very secure implant-bone bond. Use of cemented fixation is still preferred for patients with compromised health or pore bone quality that may lead to slow bone growth. In cemented fixation, the poly(methyl methacrylate) (acrylic) bone cement is polymerized in situ during surgery. This reaction must be carefully controlled, because the heat released during polymerization can lead to damage to the bone tissue. Acrylic cement has, in some cases, contributed to femoral stem loosening because it is brittle and does not bond well with the metallic implant and bone tissue. Successive loading cycles can cause cracking and failure; therefore, cemented fixation is generally not the preferred option for active or heavy people.
SUMMARY In this case study, the artificial total hip replacement was explored. The hip anatomy was first presented, which was followed by a discussion of the components and material requirements for the artificial replacement. Implant materials must be biocompatible with body tissues and fluids, corrosion resistant, and mechanically compatible with interfacing replacement/body components. The femoral stem and ball are normally made of a cold-worked stainless steel, a cast Co–Cr–Mo alloy, or a hot-forged titanium alloy. Some recent designs call for a polycrystalline aluminum oxide or zirconium oxide ball. Lightly crosslinked ultra-high-molecular-weight polyethylene is commonly used for the acetabular cup, whereas either acrylic bone cement or a porous metal surface layer is normally the fixation agent for attachment of the femoral stem (to the femur) and acetabular cup (to the pelvis).
REFERENCES Black, J., and G. Hastings (Editors), Handbook of Biomaterial Properties, Chapman & Hall, London, 1998. Davis, J. R., Handbook of Materials for Medical Devices, ASM International, Materials Park, OH, 2003.
Ratner, B. D., A. S. Hoffman, F. J. Schoen, and J. E. Lemons (Editors), Biomaterials Science: An Introduction to Materials in Medicine, Elsevier Academic Press, San Diego, CA, 2004.
DESIGN QUESTION CS4.D1 The transdermal patch has recently become popular as a mechanism for delivering drugs into the human body. (a) Cite at least one advantage of this drug-delivery system over oral administration using pills and caplets.
(b) Note the limitations on drugs that are administered by transdermal patches. (c) Make a list of the characteristics required of materials (other than the delivery drug) that are incorporated in the transdermal patch.