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睡眠障碍中心的认证标准(9)
http://www.100md.com 2018年3月1日 《世界睡眠医学杂志》 20183
     Standard

    D14PAP Therapy

    The facility must maintain equipment for the delivery of positive airway pressure therapy for sleep apnea,including remote control of the device(pressure output,device mode).

    EPolicies and Procedures

    The sleep facility must maintain written protocols,in paper or electronic form,for all testing procedures conducted in the facilityThere are additional standards in sections F and I that are required to be included in the Policy and Procedures Manual.
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    Standard

    E1Policy and Procedures Manual

    AASM accredited sleep facilities must maintain a Policy and Procedures Manual that is easily accessible,in paper form or electronically,from the control roomThe manual must contain all policies,procedures,protocols specific to the sleep facility,and all current AASM Practice Parameters and Clinical Guidelines.

    Standard

, 百拇医药     E2Protocols:PSG,MSLT,MWT,and PAP Titration

    The sleep facility must maintain written,paper or electronic format,protocols for comprehensive polysomnography,multiple sleep latency test,maintenance of wakefulness test,and titration of positive pressure therapy.

    Sleep facilities are encouraged to use “Clinical Guidelines for the Manual Titration of Positive Airway Pressure in Patients with Obstructive Sleep Apnea” in constructing PAP titration protocols.
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    Standard

    E3Other Protocols

    AASM accredited sleep facilities that conduct esophageal pressure monitoring and actigraphy must maintain protocols for these procedures.

    AASM accredited sleep facilities that test sleep patients under age 13 years must maintain population specific protocols in the Policy and Procedures Manual for comprehensive polysomnography,titration of positive pressure therapy and capnography.
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    Standard

    E4Equipment Maintenance

    A written plan for monitoring of all patientrelated equipment for electrical and mechanical safety is requiredThe written plan must include specific instructions regarding documentation of complianceThe plan must address:monthly visual inspection of equipment by staff for apparent defects; adhering to manufacturer′s recommendations for monitoring and maintenance of recording equipment; and electrical safety testing by a certified electrician or biomedical engineer to include at least annual testing for ground fault(resistance should be less than 05 ohms from chassis to ground)and chassis leakage current(amperage should be less than 100 microamps from equipment that will be in direct contact with the patient,and less than 300 microamps from equipment that will not be in direct contact with the patient,including the recording PCs)., http://www.100md.com
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