ASTM F2726-2008 Standard specification for fixation devices for tracheal tubes and other airway devices《用于气管导管和其他气道设备的固定装置的标准规范》.pdf

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1、 Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States. F 2726-08 Standard specification for fixation devices for tracheal tubes and other airway devices F 2726-08 Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Consh

2、ohocken, PA 19428-2959, United States. Contents Page FOREWORD .I INTRODUCTION . II 1. SCOPE 3 2. NORMATIVE REFERENCES 3 3. TERMS AND DEFINITIONS 4 4. *GENERAL REQUIREMENTS 5 5. *REQUIREMENTS 5 5.2 SIZE DESIGNATION. 6 5.3 MATERIALS . 6 5.4 PATIENT ATTACHMENT MECHANISM. 6 5.5 TUBE LOCKING MECHANISM 7

3、5.6 SECURITY OF ATTACHMENT 7 5.7 MAXIMUM INSTRUMENT SIZE 8 6. REQUIREMENTS FOR FIXATION DEVICES SUPPLIED STERILE. 8 7. CLEANING AND DISINFECTION OR STERILIZATION 9 8. MARKINGS. 9 9. ACCOMPANYING DOCUMENTS 10 ANNEX A (INFORMATIVE) RATIONALE 11 ANNEX B (INFORMATIVE) GUIDELINES FOR EVALUATING AND DOCUM

4、ENTING THE CLINICAL PERFORMANCE OF FIXATION DEVICES IN HUMAN SUBJECTS . 14 ANNEX C (NORMATIVE) TEST FOR SECURITY OF ATTACHMENT 16 ANNEX D (NORMATIVE) TEST METHOD TO DETERMINE THE CHANGE IN PRESSURE DROP CAUSED BY THE TUBE LOCKING MECHANISM . 18 ANNEX E (INFORMATIVE) HAZARD IDENTIFICATION FOR RISK AS

5、SESSMENT 20 ANNEX F (INFORMATIVE) GUIDANCE ON MATERIALS AND DESIGN. 22 ANNEX G (INFORMATIVE) BIBLIOGRAPHY 23 F 2726-08 i Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States. Foreword This ASTM standard was developed as an American Nationa

6、l Standard by ASTM Committee F29, Anesthesia and Respiratory Equipment, Subcommittee F29.12, Airways, Task Group 29.12.08, Tracheal Tube Fixation Devices, in the format of an ISO standard to serve as a guide for future work as a new ISO Standard. This is the first edition of this standard. F 2726-08

7、 ii Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States. Introduction This ASTM Standard provides the essential requirements for the design of fixation devices for tracheal tubes and other airway devices, hereafter referred to as fixation

8、 devices. These devices are intended to secure and stabilize the position of tracheal tubes and other airway devices. This ASTM standard specifies the dimensions and method of size designation of fixation devices so that the operator will know which airway device(s) will be size compatible with thes

9、e fixation devices. Certain fixation devices which are devised for specialized applications are not covered, although most may be classified by the sizing and dimensions required by this standard. Unintentional movement of the tracheal tube or other airway device continues to be a leading cause of p

10、atient injury. Fixation devices are designed to stabilize and fix the position of tracheal tubes and other airway devices to prevent injury. Commercially available fixation devices typically differ from the classical means to secure tracheal tubes or other airway devices (e.g. adhesive or cloth tape

11、) by providing clamps, clips, or other adhesive or non-adhesive based fasteners intended to attach the device to the head of the patient and to secure the tracheal tube or other airway device in one place. The 2005 American Heart Association 3recommends the use of fixation devices rather than tape.

12、These devices may be easier to use and more comfortable for the patient than the classical means. They offer the advantage of ease of relocation or reapplication on the same patient. While these devices have reduced injuries related to the use of adhesive surgical tape, many injuries are still cause

13、d by deficiencies in the manufactured devices. Many devices lack the integrity, security, strength, and immobilization characteristics needed. Some devices, if used improperly, have been demonstrated to create the additional risk of tissue ischemia and necrosis caused by excessive pressure. Several

14、designs have proven difficult to use, especially in emergency conditions, due to lack of clear instructions, markings, and labeling. Annexes C, D, and E are normative; Annexes A, B, F, G, and H are informative. Annex A contains rationale statements for some of the requirements of this part of ISO. T

15、he clauses and sub classes marked with an asterisk (*) after their number have corresponding rationale contained in annex A, included to provide additional insight into the reasoning that led to the requirements and recommendations that have been incorporated in this standard. It is considered that

16、knowledge of the reasons for the requirements will not only facilitate the proper application of this standard, but will expedite any subsequent revisions. F 2726-08 Page 3 Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States. 1. Scope 1.1

17、 *This standard covers basic safety and essential performance requirements for fixation devices designed to be attached to the head, face, or mouth of the patient and equipped with a means to secure and stabilize a tracheal tube or other airway device in its intended position. Devices within the sco

18、pe of this standard may be provided with a wide variety of patient attachment mechanisms and tube locking mechanisms. 1.2 *Devices intended to secure tracheostomy tubes are outside the scope of this standard. NOTE These requirements are addressed in ISO 5366-11and 5366-32. 1.3 *Fixation devices inte

19、nded to secure devices such as gastric tubes, feeding tubes and suction catheters are outside the scope of this standard. 1.4 Flammability of fixation devices, for example if used in the presence of certain flammable anesthetics, electrosurgical units, or lasers is a well-recognized hazard that is o

20、utside the scope of this standard. See Annex F for guidance. 2. Normative references The following normative documents contain provisions which, through reference in this text, constitute provisions of this Standard. For dated references, subsequent amendments to, or revisions of, any of these publi

21、cations do not apply. However, parties to agreements based on this Standard are encouraged to investigate the possibility of applying the most recent editions of the normative documents indicated below. For undated references, the latest edition of the normative document referred to applies. Members

22、 of ISO and IEC maintain registers of currently valid Standards. ASTM D 2665-07, Standard specification for poly (vinyl chloride) (PVC) plastic drain, waste, and vent pipe and fittings ASTM F 1573, Standard specification for anesthetic equipment-Oropharyngeal and nasopharyngeal airways ASTM F 2560-2

23、006, Anesthetic and respiratory equipment Standard specification for supralaryngeal airways and connectors ISO 4135, Anaesthesiology-vocabulary ISO 5361:2005, Anaesthetic and respiratory equipment - Tracheal tubes and connectors ISO 5364:2001 Anaesthetic and respiratory equipment - Oropharyngeal air

24、ways ISO 5367:2000 Breathing tubes intended for use with anaesthetic apparatus and ventilators ISO 7000, Graphical symbols ISO 10993-1, Biological evaluation of medical devices Part 1: Guidance on selection of tests. ISO 11134, Sterilization of healthcare products-requirements for validation and rou

25、tine control Industrial moist heat sterilization ISO 11135, Medical Devices Validation and routine control of ethylene oxide sterilization F 2726-08 Page 4 Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States. ISO 11137, Sterilization of h

26、ealthcare products - Requirements for validation and routine control Radiation sterilization ISO 11607, Packaging for terminally sterilized medical devices ISO 11990, Optics and optical instruments Lasers and laser-related equipment Determination of laser resistance of tracheal tube shafts ISO 11991

27、, Guidance on airway management during laser surgery of upper airway ISO 14155-1, Clinical investigation of medical devices for human subjects - Part 1: General requirements ISO 14155-2, Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans ISO 14408, Tr

28、acheal tubes and related treatments designed for resistance to ignition by a laser - Requirements for marking, labeling and accompanying information ISO 14971, Medical devices Applications of risk management to medical devices 3. Terms and definitions For the purposes of this Standard, the following

29、 terms and definitions apply: 3.1 fixation device device that contains a patient attachment mechanism and a tube locking mechanism to secure and stabilize a tracheal tube or other airway device in its intended position. NOTE The fixation device may incorporate a bite block. 3.2 machine side the side

30、 of the fixation device intended to face away from the patient and toward the breathing system 3.3 patient attachment mechanism the portion of the fixation device that stabilizes the device on the patient NOTE 1 The patient attachment mechanism may be attached to the head, face, or mouth. NOTE 2 Pat

31、ient attachment mechanisms include tape, straps, bands, wires, or pads that either surround the head and/or attach directly to the face. 3.4 patient side the surface of the fixation device intended to be placed on or inserted into the patient 3.5 single fault condition condition in which a single me

32、ans for protection against a safety hazard in equipment is defective or a single external abnormal condition is present F 2726-08 Page 5 Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States. 3.6 tube locking mechanism the portion of the fi

33、xation device that locks the tracheal tube or other airway device to the patient attachment mechanism NOTE The tube locking mechanism may consist of tape, adhesives, fasteners, locks, collets (which squeeze and compress the tracheal tube or other airway device), clips or other means to stabilize the

34、 tracheal tube or other airway device. 4. *General requirements This standard specifies requirements that are generally applicable to risks associated with fixation devices. 4.1 An established risk management process shall be applied to the design of the device. NOTE See Annex E for a list of identi

35、fied hazards. 4.2 Fixation devices shall, when used and maintained in accordance with the instructions of the manufacturer, present no risks that are not reduced to an acceptable level using risk management procedures in accordance with ISO 14971 and which are connected with their intended applicati

36、on in normal condition and single fault condition. 4.3 Fixation devices shall, when transported, stored, installed, operated in normal use as intended, and maintained according to the instructions of the manufacturer, minimize safety hazards which could reasonably be foreseen, in normal condition an

37、d single fault condition. 4.4 *It is recognized that the manufacturer might not be able to follow all the processes identified in this standard for each constituent component of the fixation device, such as proprietary components, subsystems of non-medical origin, and legacy devices. In this case, t

38、he manufacturer should take special account of the need for additional risk control measures. 4.5 The manufacturer may use type tests different from those detailed within this standard, if an equivalent degree of safety is obtained. However, in the event of dispute, the methods specified herein shal

39、l be used as the reference methods. 5. *Requirements NOTE The requirements of this standard were developed using the Hazard Identification for Risk Assessment in Annex E. 5.1 *Fixation devices shall prevent unintended movement of tracheal tubes or other airway devices in those head and neck position

40、s and patient positions for which the device is intended to be used. The following head and neck positions shall include at least a 30o change from a neutral position: a. flexion b. extension c. right and left rotation d. right and left lateral flexion (tilt) F 2726-08 Page 6 Copyright ASTM Internat

41、ional, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States. All these shall be performed in the following patient body positions: a. supine b. prone c. 30-degree Trendelenburg (head down) d. 60-degree sitting e. 90-degree lateral (right and left) Compliance shall be t

42、ested by functional testing. If clinical studies are performed, the clinical studies shall document measurements taken during the conditions for which performance is claimed. The clinical studies shall comply with the requirements of ISO 14155-1 and ISO 14155-2. NOTE See also Annex B and Annex E. 5.

43、2 Size designation The size of a fixation device shall be designated using the same convention as that of the tracheal tube or other airway device that it is intended to secure. Devices that are intended for a range of sizes shall be marked with the corresponding range. a. For devices intended to be

44、 used with tracheal tubes, the size designation shall be the ID size of the tracheal tube in mm, as indicated in ISO 5361. b. For devices intended to be used with supralaryngeal airways, the range of sizes shall be from 0 to 6 for the smallest to largest size devices, as indicated in ASTM F 2560. Th

45、e smallest increment permitted is 0.5. The transition size from pediatric to adult is size 3. c. For devices intended to be used with oropharyngeal airways, the size shall be the designated length in cm of the airway, as indicated in ISO 5365. d. For devices intended to be used with nasopharyngeal a

46、irways, the size shall be the inside diameter in mm, as designated in ASTM F1573. 5.3 Materials Fixation devices, including patient attachment mechanisms, tube locking mechanisms, and all related accessories in their ready-for-use state after any preparation for use recommended by the manufacturer,

47、shall satisfy appropriate biological safety testing, as indicated in ISO 10993-1. Initial biocompatibility evaluation tests shall include all materials in the fixation device. These shall be tested as external communicating, tissue/bone/dentin communicating, and 24 hour duration. NOTE See Annex F fo

48、r guidance on materials and design. 5.4 Patient attachment mechanism 5.4.1 The patient attachment mechanism shall be attached or integral to the fixation device and not require assembly by the user before use. Compliance shall be tested by examination. 5.4.2 *For tracheal tube sizes 4.0, supralaryng

49、eal airway sizes 1.5 and oropharyngeal airway sizes 5, it shall be possible to affix the patient attachment mechanism to the head or face of the patient in such a manner that movement under a strain of 45 N shall not exceed 1 cm in the ventral axis direction. For tracheal tube sizes 90 % relative humidity for at least 1 hour. D.3.1.2. Remove the tracheal tube or other airway device from the environmental chamber and connect the tracheal tube or other airway device connector to the apparatus as shown in Figure D.1. Flow air a