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Medical electrical equipment — Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency 医用电气设备第2-80部分:通气不足通气支持设备基本安全和基本性能的特殊要求
发布日期: 2024-08-28
注1条款AA.2中包含了本子条款的指导或理由。 本文件适用于201.3.302中定义的用于通气功能不全的通气支持设备(以下也称为ME设备)及其附件的基本安全性和基本性能: -旨在用于家庭保健环境中; 注2:在家庭医疗保健环境中,驱动通气支持设备的电源通常不可靠。 注3此类通气支持设备也可用于专业医疗机构。 -旨在供非专业操作员使用; -预期用于通气功能不全或衰竭的患者,其中最脆弱的患者可能会因失去这种人工通气而受伤;-拟用于运输操作用途;和 -不适用于依赖人工通气来维持生命的患者。 实施例1患有中度至重度慢性阻塞性肺病(COPD)、中度肌萎缩侧索硬化(ALS)、重度支气管肺发育不良或肌营养不良的患者。 通气支持设备不被认为使用生理闭环控制系统,除非其使用生理患者变量来调整人工通气治疗设置。 本文件也适用于制造商打算连接到用于通气功能不全的通气支持设备的呼吸机呼吸系统的附件,其中这些附件的特性会影响用于通气功能不全的通气支持设备的基本安全性或基本性能。实施例2呼吸器、连接器、水阱、呼气阀、加湿器、呼吸系统过滤器、外部电源、分布式报警系统。 如果一个条款或子条款特别旨在仅适用于ME设备,或仅适用于ME系统,该条款或子条款的标题和内容将如此说明。如果不是这种情况,该条款或子条款适用于相关的ME设备和ME系统。 除了IEC 60601?1:20 05+AMD1:2012+AMD2:2020,7.2.13和8.4.1。 注4其他信息见IEC 60601?1:2005+AMD1:2012+AMD2:2020,4.2。 注5关于为给定患者选择适当呼吸机的指南,请参见ISO/TR 21954。本文件未规定以下方面的要求: -ISO 80601中给出的用于危重护理应用的依赖呼吸机的患者的呼吸机或附件?2?12; -ISO 80601中规定的用于麻醉应用的呼吸机或附件?2?13; -ISO 80601中规定的用于紧急医疗服务环境的呼吸机或附件?2?84; -ISO 80601中规定的用于家庭医疗环境中依赖呼吸机的患者的呼吸机或附件?2?72; -ISO 80601中给出的用于通气障碍的通气支持设备或附件?2?79; -睡眠呼吸暂停治疗ME设备,ISO 80601?2?70; -高频喷射通风机(HFJV),在ISO 80601?2?87;-高频振荡呼吸机; -ISO 80601中规定的呼吸高流量设备?2?90; 注6通气支持设备可结合高流量治疗操作模式,但该模式仅适用于自主呼吸患者。 -用户驱动的复苏器,其在ISO 10651-4中给出; -气体动力紧急复苏器,其在ISO 10651-5中给出; -氧疗恒流ME设备;和 -胸甲或“铁肺”通气设备。

NOTE 1       There is guidance or rationale for this subclause contained in Clause AA.2.

This document applies to the basic safety and essential performance of ventilatory support equipment, as defined in 201.3.302, for ventilatory insufficiency, as defined in 201.3.302, hereafter also referred to as ME equipment, in combination with its accessories:

    intended for use in the home healthcare environment;

NOTE 2     In the home healthcare environment, the supply mains driving the ventilatory support equipment is often not reliable.

NOTE 3     Such ventilatory support equipment can also be used in professional health care facilities.

    intended for use by a lay operator;

    intended for use with patients who have ventilatory insufficiency or failure, the most fragile of which would likely experience injury with the loss of this artificial ventilation;

    intended for transit-operable use; and

    not intended for patients who are dependent on artificial ventilation for their immediate life support.

EXAMPLE 1        Patients with moderate to severe chronic obstructive pulmonary disease (COPD), moderate amyotrophic lateral sclerosis (ALS), severe bronchopulmonary dysplasia or muscular dystrophy.

Ventilatory support equipment is not considered to use a physiologic closed-loop control system unless it uses a physiological patient variable to adjust the artificial ventilation therapy settings.

This document is also applicable to those accessories intended by their manufacturer to be connected to the ventilator breathing system of ventilatory support equipment for ventilatory insufficiency, where the characteristics of those accessories can affect the basic safety or essential performance of the ventilatory support equipment for ventilatory insufficiency.

EXAMPLE 2        Breathing sets, connectors, water traps, expiratory valve, humidifier, breathing system filter, external electrical power source, distributed alarm system.

If a clause or subclause is specifically intended to be applicable to ME equipment only, or to ME systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME equipment and to ME systems, as relevant.

Hazards inherent in the intended physiological function of ME equipment or ME systems within the scope of this document are not covered by specific requirements in this document except in IEC 606011:2005+AMD1:2012+AMD2:2020, 7.2.13 and 8.4.1.

NOTE 4       Additional information can be found in IEC 606011:2005+AMD1:2012+AMD2:2020, 4.2.

NOTE 5       See ISO/TR 21954 for guidance on the selection of the appropriate ventilator for a given patient. 

This document does not specify the requirements for:

    ventilators or accessories for ventilator-dependent patients intended for critical care applications, which are given in ISO 806012?12;

    ventilators or accessories intended for anaesthetic applications, which are given in ISO 806012?13;

    ventilators or accessories intended for the emergency medical services environment, which are given in ISO 806012?84;

    ventilators or accessories intended for ventilator-dependent patients in the home healthcare environment, which are given in ISO 806012?72;

    ventilatory support equipment or accessories intended for ventilatory impairment, which are given in ISO 806012?79;

    sleep apnoea therapy ME equipment, which are given in ISO 806012?70;

    high-frequency jet ventilators (HFJVs), which are given in ISO 80601?2?87;

    high-frequency oscillatory ventilators (HFOVs);

    respiratory high flow equipment, which are given in ISO 806012?90;

NOTE 6     Ventilatory support equipment can incorporate high-flow therapy operational mode, but such a mode is only for spontaneously breathing patients.

    user-powered resuscitators, which are given in ISO 10651-4;

    gas-powered emergency resuscitators, which are given in ISO 10651-5;

    oxygen therapy constant flow ME equipment; and

    cuirass or “iron-lung” ventilation equipment.

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归口单位: ISO/TC 121/SC 3
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