BS ISO 14242-3-2009 Implants for surgery - Wear of total hip-joint prostheses - Loading and displacement parameters for orbital bearing type wear testing machines and corresponding.pdf

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1、BS ISO14242-3:2009ICS 11.040.40NO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAWBRITISH STANDARDImplants for surgery Wear of total hip-jointprosthesesPart 3: Loading and displacementparameters for orbital bearingtype wear testing machines andcorresponding environmentalconditions

2、 for testThis British Standardwas published underthe authority of theStandards Policy andStrategy Committee on 30November 2009 BSI 2009ISBN 978 0 580 57753 6Amendments/corrigenda issued since publicationDate CommentsBS ISO 14242-3:2009National forewordThis British Standard is the UK implementation o

3、f ISO 14242-3:2009.The UK participation in its preparation was entrusted to TechnicalCommittee CH/150/4, Bone and joint replacements.A list of organizations represented on this committee can be obtained onrequest to its secretary.This publication does not purport to include all the necessary provisi

4、onsof a contract. Users are responsible for its correct application.Compliance with a British Standard cannot confer immunityfrom legal obligations.BS ISO 14242-3:2009Reference numberISO 14242-3:2009(E)ISO 2009INTERNATIONAL STANDARD ISO14242-3First edition2009-03-15Implants for surgery Wear of total

5、 hip-joint prostheses Part 3: Loading and displacement parameters for orbital bearing type wear testing machines and corresponding environmental conditions for test Implants chirurgicaux Usure des prothses totales de larticulation de la hanche Partie 3: Paramtres de charge et de dplacement pour mach

6、ines dessai dusure du type orbital de maintien et conditions environnementales correspondantes dessai BS ISO 14242-3:2009ISO 14242-3:2009(E) PDF disclaimer This PDF file may contain embedded typefaces. In accordance with Adobes licensing policy, this file may be printed or viewed but shall not be ed

7、ited unless the typefaces which are embedded are licensed to and installed on the computer performing the editing. In downloading this file, parties accept therein the responsibility of not infringing Adobes licensing policy. The ISO Central Secretariat accepts no liability in this area. Adobe is a

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9、odies. In the unlikely event that a problem relating to it is found, please inform the Central Secretariat at the address given below. COPYRIGHT PROTECTED DOCUMENT ISO 2009 All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized in any form or by an

10、y means, electronic or mechanical, including photocopying and microfilm, without permission in writing from either ISO at the address below or ISOs member body in the country of the requester. ISO copyright office Case postale 56 CH-1211 Geneva 20 Tel. + 41 22 749 01 11 Fax + 41 22 749 09 47 E-mail

11、copyrightiso.org Web www.iso.org Published in Switzerland ii ISO 2009 All rights reservedBS ISO 14242-3:2009ISO 14242-3:2009(E) ISO 2009 All rights reserved iiiContents Page Foreword iv Introduction v 1 Scope . 1 2 Normative references . 1 3 Terms and definitions. 1 4 Principle. 2 5 Reagents and tes

12、t specimens . 2 6 Apparatus 3 7 Procedure 6 8 Test report . 7 9 Disposal of test specimen . 8 Bibliography . 9 BS ISO 14242-3:2009ISO 14242-3:2009(E) iv ISO 2009 All rights reservedForeword ISO (the International Organization for Standardization) is a worldwide federation of national standards bodie

13、s (ISO member bodies). The work of preparing International Standards is normally carried out through ISO technical committees. Each member body interested in a subject for which a technical committee has been established has the right to be represented on that committee. International organizations,

14、 governmental and non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization. International Standards are drafted in accordance with the rules given in the ISO

15、/IEC Directives, Part 2. The main task of technical committees is to prepare International Standards. Draft International Standards adopted by the technical committees are circulated to the member bodies for voting. Publication as an International Standard requires approval by at least 75 % of the m

16、ember bodies casting a vote. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. ISO shall not be held responsible for identifying any or all such patent rights. ISO 14242-3 was prepared by Technical Committee ISO/TC 150, Implants for

17、 surgery, Subcommittee SC 4, Bone and joint replacements. ISO 14242 consists of the following parts, under the general title Implants for surgery Wear of total hip-joint prostheses: Part 1: Loading and displacement parameters for wear-testing machines and corresponding environmental conditions for t

18、est Part 2: Methods of measurement Part 3: Loading and displacement parameters for orbital bearing type wear testing machines and corresponding environmental conditions for test BS ISO 14242-3:2009ISO 14242-3:2009(E) ISO 2009 All rights reserved vIntroduction The orbital bearing hip wear simulator (

19、OBM) is widely used and has been successful in evaluating the wear properties of Total Hip Arthroplasty (THA) articulating surfaces. These test results have been shown to correlate well with clinical experience. Since this type of test machine is widely used, it is important that the parameters be s

20、tandardized to make the results more uniform and comparable between laboratories. This test method differs from that in ISO 14242-1 in the articulating motion of the test. Although the motion of the OBM is simpler and less anatomic than the motion described in ISO 14242-1, OBM hip simulators have be

21、en used to evaluate the wear of THA articulating components for more than 25 years. The equipment is used globally for wear testing of THA components, and has been very successful in reproducing the types and amounts of wear that occur in vivo with a wide variety of bearing materials, including poly

22、ethylene, metals and ceramics. Because of this, tests on OBM machines have provided very accurate predictions of the subsequent clinical performance of newly developed materials. This is particularly true for the new crosslinked polyethylenes. Several recent reports with more than five years of foll

23、ow up have shown percent reductions in wear, compared to historical polyethylene, that are very close to those that were predicted as much as ten years earlier in tests run on OBM hip simulators. BS ISO 14242-3:2009BS ISO 14242-3:2009INTERNATIONAL STANDARD ISO 14242-3:2009(E) ISO 2009 All rights res

24、erved 1Implants for surgery Wear of total hip-joint prostheses Part 3: Loading and displacement parameters for orbital bearing type wear testing machines and corresponding environmental conditions for test 1 Scope This part of ISO 14242 specifies relative angular movement between articulating compon

25、ents, the pattern of the applied force, speed and duration of testing, sample configuration and test environment to be used for the orbital bearing type wear testing of total hip joint prostheses. 2 Normative references The following referenced documents are indispensable for the application of this

26、 document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. ISO 14242-2, Implants for surgery Wear of total hip joint prostheses Part 2: Methods of measurement 3 Terms and definitions For t

27、he purposes of this document, the following terms and definitions apply. 3.1 abduction adduction motion about an axis arranged in an anterior-posterior direction through the hip joint NOTE 1 Movement of the femur away from the midline of the torso is termed abduction. Movement of the femur toward th

28、e torso midline is known as adduction. NOTE 2 Angular movement is shown in Figure 1 a). 3.2 flexion extension motion that occurs about a transverse axis through the hip joint NOTE 1 Movement at a joint, which decreases the angle between the torso and the femur, is termed flexion. The opposite action

29、 is termed extension, where the angle between the torso and the femur is increased. NOTE 2 Angular movement is shown in Figure 1 b). BS ISO 14242-3:2009ISO 14242-3:2009(E) 2 ISO 2009 All rights reserved3.3 inward rotation outward rotation component of internal/external motion NOTE 1 The OBM hip simu

30、lator does not apply an independent “inward/outward” motion to the hip (i.e., about the long axis of the femur.) However, Saikko et al.8pointed out that the anti-rotation lever that is connected to each test chamber of an OBM machine induces a component of internal-external rotation to the motion pa

31、th, effectively converting the OBM into a 3-axis machine. The mechanism of the OBM simulator induces a crossing-path component to the relative motion of the bearing surfaces. Because of this, as was demonstrated in detail by Wang et al.13, the magnitude of the shear stress and the amount of change o

32、f direction of this stress during the loaded part of the gait cycle are comparable to that which occurs in a hip replacement in vivo. NOTE 2 Angular movement is shown in Figure 1 c). 3.4 polar axis axis of the acetabular component, which intersects the centre of the spherical articulating surface an

33、d is perpendicular to the plane of the flange or, if no flange is present, perpendicular to the plane of the entry diameter 4 Principle The femoral and acetabular components of a test specimen are placed in position in their normal configuration and the apparatus transmits a specified time-dependent

34、 force between the components together with specified relative angular displacements. A control specimen, if polymers are the object of investigation, is subjected to the same time-dependent force to determine the creep of the test specimen and/or the amount of mass change due to fluid transfer. The

35、 test takes place in a controlled environment simulating physiological conditions. 5 Reagents and test specimens 5.1 Fluid test medium, calf serum approximately 25 % volume fraction diluted with de-ionized water (balance). The fluid test medium should be filtered through a filter of pore size 2 m an

36、d have a protein mass concentration of not less than 17 g/l. To minimize microbial contamination, the fluid test medium should be stored frozen until required for test. An anti-microbial reagent (such as sodium azide) may be added. Such reagents can be potentially hazardous. Routine monitoring of th

37、e pH of the fluid test medium can be undertaken. If it is, the values should be included in the test report (see Clause 8). NOTE The use of a fluid test medium of non-biological origin can be considered when performance requirements relating to this test method are being decided. 5.2 Test specimen,

38、femoral head and acetabular components. The acetabular component shall have the articulating surface attached by its normal immediate backing (for example bone cement or a machined replica of the inner surface of the backing) unless this is impractical due to physical features of the implant system.

39、 If the component forming the articulating surface is fixed to the backing by a rim/snap-fit system the machined replica shall provide the same fixation conditions. If it is not practical to use the normal backing or cement fixation due to physical features of the implant system, the support system

40、for the acetabular component should represent normal design features and conditions of use but should allow removal of the component for measurement of wear without destruction. BS ISO 14242-3:2009ISO 14242-3:2009(E) ISO 2009 All rights reserved 3Consideration should be given to the condition of the

41、 test specimen. This condition should represent the final sterile implanted condition where possible unless processing effects are under investigation. NOTE It can be useful to characterize specimens prior to testing. Profilometry, hardness, photomicrography and other analytical techniques can be us

42、ed. 5.3 Control specimen, identical to test specimen. Consideration should be given to the condition of the control specimen. This condition should represent the final sterile implanted condition where possible unless processing effects are under investigation. NOTE It can be useful to characterize

43、specimens prior to testing. Profilometry, hardness, photomicrography and other analytical techniques can be used. 6 Apparatus 6.1 Testing machine, capable of producing the angular displacements prescribed in Figures 1 and 2 in association with the corresponding forces prescribed in Figures 1 and 3 a

44、nd operating at a frequency of 1 Hz 0,1 Hz. 6.2 Means of mounting and enclosing the test specimen, using a corrosion resistant material, capable of holding femoral and acetabular components, using attachment methods comparable to the intended anatomical fixation and an enclosure that is capable of i

45、solating the test specimen to prevent third body contamination from the test machine and the atmosphere. NOTE Consideration should be given to the support material used to mount femoral and acetabular components to ensure representative force transfer and stress conditions. 6.3 Means of aligning and

46、 positioning the femoral component of the test specimen, in the inferior position so that its axis is situated at the centre of the axes of rotation of the test machine and so that the same position and orientation can be produced following removal of the component for measurement or cleaning, if re

47、quired. NOTE For a modular component, the stem of the implant can be replaced by a support that has an identical cone and assures reproducible positioning of the head. 6.4 Means of aligning and positioning the acetabular component, of the test specimen so that its axis is situated at the centre of t

48、he axes of rotation of the test machine and so that the same position and orientation can be reproduced following removal of the component for measurement. 6.5 Motion control system, capable of generating the angular movements of the femoral component given in Figures 1 and 2 with an accuracy of 3 a

49、t the maxima and minima of the motion and 1 % of the cycle time for phasing. 6.6 Force control system, capable of generating a force whose direction is shown in Figure 1 and which varies as shown in Figure 3 and maintaining the magnitude of the maxima and minima of this force cycle to a tolerance of 3 % of the maximum force value for the cycle and 1 % of the cycle time for phasing. 6.7 Lubrication system, capable of maintaining the contact surfaces immersed in the fluid test medium and having a minimum availa