LOINC Panel Details

Panel: 74725-3 - Patient safety event report - hospital - device or medical &or surgical supply, including health information technology - version 1.2:-:Pt:^Patient:-:AHRQ

• 74725-3 - Patient safety event report - hospital - device or medical &or surgical supply, including health information technology - version 1.2:-:Pt:^Patient:-:AHRQ (Patient Safety Event Report - Hospital: Device or Medical/Surgical Supply, including Health Information Technology - Version 1.2) (Seq: 349, Type: N/A) None
  • 74081-1 - Patient safety event:ID:Pt:^Event:Nom:AHRQ (Event ID:) (Seq: 1, Type: N/A) None

    Required: R
  • 30947-6 - Date form completed (Initial Report Date (HERF Q1):) (Seq: 2, Type: N/A) {mm/dd/yyyy}

    Required: R
  • 74724-6 - Best description of the event or unsafe condition:Find:Pt:^Event:Nom:AHRQ (Which of the following best describes the event or unsafe condition?) (Seq: 3, Type: N/A) None

    Required: R
  • 74723-8 - Device involved in patient safety event or unsafe condition:Type:Pt:{Device}:Nom:AHRQ (What type of device was involved in the event or unsafe condition?) (Seq: 4, Type: N/A) None

    Required: R
  • 74722-0 - At the time of the event, the device was placed within the patient's tissue:Find:Pt:^Patient:Ord:AHRQ (At the time of the event, was the device placed within the patient's tissue?) (Seq: 5, Type: N/A) None

    Required: C
  • 74721-2 - Event resulted in the device being removed:Find:Pt:^Event:Ord:AHRQ (Did the event result in the device being removed?) (Seq: 6, Type: N/A) None

    Required: C
  • 74720-4 - Device name (What is the name (brand or generic) of the device, product, software, or medical/surgical supply?) (Seq: 7, Type: N/A) None

    Required: O
  • 74719-6 - Manufacturer name (What is the name of the manufacturer?) (Seq: 8, Type: N/A) None

    Required: O
  • 74718-8 - Device ID (Which of the following identifiers are known?) (Seq: 9, Type: N/A) None

    Required: R
  • 74717-0 - Model # (What is the model number?) (Seq: 10, Type: N/A) None

    Required: C
  • 55081-4 - Product version code:ID:Pt:Software:Nom: (Seq: 11, Type: N/A) None

    Required: C
  • 74716-2 - Vendor firmware version (What is the firmware version?) (Seq: 12, Type: N/A) None

    Required: C
  • 74715-4 - Serial # (What is the serial number?) (Seq: 13, Type: N/A) None

    Required: C
  • 74714-7 - Lot or batch no. (What is the lot or batch number?) (Seq: 14, Type: N/A) None

    Required: C
  • 74713-9 - Other UDI [Type] (What is the type of other unique product identifier?) (Seq: 15, Type: N/A) None

    Required: C
  • 74726-1 - Other UDI (What is the other unique product identifier?) (Seq: 16, Type: N/A) None

    Required: C
  • 74712-1 - Expiration date (What is the expiration date?) (Seq: 17, Type: N/A) {mm/dd/yyyy}

    Required: C
  • 74711-3 - UDI (What is the Unique Device Identifier (UDI)?) (Seq: 18, Type: N/A) None

    Required: C
  • 74710-5 - Asset tag number (What is the asset tag number?) (Seq: 19, Type: N/A) None

    Required: C
  • 74709-7 - Device intended for single use was involved in the event or unsafe condition:Find:Pt:^Event:Ord:AHRQ (Was a device intended for single use involved in the event or unsafe condition (including use of a reprocessed single-use device)?) (Seq: 20, Type: N/A) None

    Required: R
  • 74708-9 - Device intended for single use was reused in the event or unsafe condition:Find:Pt:^Event:Ord:AHRQ (Was a device intended for a single use reused in the event or unsafe condition?) (Seq: 21, Type: N/A) None

    Required: C
  • 74707-1 - Medication or other substance was involved:Find:Pt:^Event:Ord:AHRQ (Did the event or unsafe condition involve a medication or other substance?) (Seq: 22, Type: N/A) None

    Required: R
  • 74706-3 - Health information technology device was involved:Find:Pt:^Event:Ord:AHRQ (Did the event or unsafe condition involve an HIT device?) (Seq: 23, Type: N/A) None

    Required: C
  • 74705-5 - Best characterization of health information technology device:Find:Pt:{Device}:Nom:AHRQ (Which of the following best characterizes the type of HIT device related to the event or unsafe condition?) (Seq: 24, Type: N/A) None

    Required: C
  • 74704-8 - Administrative or billing system component:Type:Pt:Administrative or billing system:Nom:AHRQ (Which component of the administrative/billing system?) (Seq: 25, Type: N/A) None

    Required: C
  • 74703-0 - Electronic health record system component:Type:Pt:Electronic health record:Nom:AHRQ (Which type or component of the EHR?) (Seq: 26, Type: N/A) None

    Required: C
  • 74702-2 - Circumstances involving the health information technology device in the event or unsafe condition:Type:Pt:{Device}:Nom:AHRQ (Which of the following describes the circumstances involving the HIT device in the event or unsafe condition?) (Seq: 27, Type: N/A) None

    Required: C
  • 74701-4 - Problem that resulted from the equipment or device function problem:Type:Pt:{Device}:Nom:AHRQ (Which problem(s) resulted from the equipment/device function problem?) (Seq: 28, Type: N/A) None

    Required: C
  • 74700-6 - Ergonomics or human &or device interface issue:Type:Pt:{Device}:Nom:AHRQ (Which ergonomics or human/device interface issue(s)?) (Seq: 29, Type: N/A) None

    Required: C