Form 139 Adult Heart and HeartLung Status 3 Initial Justification

Data System for Organ Procurement and Transplantation Network

139. Adult Heart and HeartLung Status 3 Initial Justification Form Medical Urgency Data_Form.xlsx

Adult Heart and HeartLung Status 3 Initial Justification Form Medical Urgency Data

OMB: 0915-0157

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Adult Heart and HeartLung Status 3 Initial Justification Form Medical Urgency Data
Fields to be completed by members



Form Section Field Label Notes
Status 3 Justification Form
Section IV
Dischargeable left ventricular assist device (LVAD) for discretionary 30 days
Status 3 Justification Form
Section IV
Multiple inotropes or a single high dose inotrope and hemodynamic monitoring
Status 3 Justification Form
Section IV
Select one of the following
Status 3 Justification Form
Section IV
Candidate is supported by either
Status 3 Justification Form
Section IV
A continuous infusion of at least one high dose intravenous inotrope
Status 3 Justification Form
Section IV
Was the candidate on inotropic or mechanical support at the time cardiac index was obtained?
Status 3 Justification Form
Section IV
Cardiac index
Status 3 Justification Form
Section IV
Cardiac index - Test Date
Status 3 Justification Form
Section IV
Cardiac index - Test Time
Status 3 Justification Form
Section IV
Pulmonary capillary wedge pressure
Status 3 Justification Form
Section IV
Pulmonary capillary wedge pressure - Test Date
Status 3 Justification Form
Section IV
Pulmonary capillary wedge pressure - Test Time
Status 3 Justification Form
Section IV
Systolic blood pressure
Status 3 Justification Form
Section IV
Systolic blood pressure - Test Date
Status 3 Justification Form
Section IV
Systolic blood pressure - Test Time
Status 3 Justification Form
Section IV
Mechanical circulatory support device (MCSD) with hemolysis
Status 3 Justification Form
Section IV
Two separate samples collected within 48 hours of each other confirming markers of active hemolysis as evidenced by at least two of the following
Status 3 Justification Form
Section IV
Mechanical circulatory support device (MCSD) with pump thrombosis
Status 3 Justification Form
Section IV
Mechanical circulatory support device (MCSD) with right heart failure
Status 3 Justification Form
Section IV
Dobutamine
Status 3 Justification Form
Section IV
Dobutamine - Date of Initiation
Status 3 Justification Form
Section IV
Dopamine
Status 3 Justification Form
Section IV
Dopamine - Date of Initiation
Status 3 Justification Form
Section IV
Epinephrine
Status 3 Justification Form
Section IV
Epinephrine - Date of Initiation
Status 3 Justification Form
Section IV
Milrinone
Status 3 Justification Form
Section IV
Milrinone - Date of Initiation
Status 3 Justification Form
Section IV
Inhaled nitric oxide
Status 3 Justification Form
Section IV
Inhaled nitric oxide - Date of Initiation
Status 3 Justification Form
Section IV
Intravenous prostacyclin
Status 3 Justification Form
Section IV
Intravenous prostacyclin - Date of Initiation
Status 3 Justification Form
Section IV
Pulmonary capillary wedge pressure
Status 3 Justification Form
Section IV
Pulmonary capillary wedge pressure - Test Date
Status 3 Justification Form
Section IV
Pulmonary capillary wedge pressure - Test Time
Status 3 Justification Form
Section IV
Central venous pressure
Status 3 Justification Form
Section IV
Central venous pressure - Test Date
Status 3 Justification Form
Section IV
Central venous pressure - Test Time
Status 3 Justification Form
Section IV
Mechanical circulatory support device (MCSD) with device infection
Status 3 Justification Form
Section IV
Mechanical circulatory support device (MCSD) with mucosal bleeding
Status 3 Justification Form
Section IV
Number of hospitalizations for mucosal bleeding within the past six months
Status 3 Justification Form
Section IV
Mechanical circulatory support device (MCSD) with aortic insufficiency (AI)
Status 3 Justification Form
Section IV
Veno-arterial extracorporeal membrane oxygenation (VA ECMO) after 7 days
Status 3 Justification Form
Section IV
Non-dischargeable, surgically implanted, non-endovascular left ventricular assist device (LVAD) after 14 days
Status 3 Justification Form
Section IV
Percutaneous endovascular circulatory support device after 14 days
Status 3 Justification Form
Section IV
Intra-aortic balloon pump after 14 days
Status 3 Justification Form
Section IV
Mechanical Circulatory Support Device (MCSD) with life threatening ventricular arrhythmia after 7 days
Status 3 Justification Form
Section IV
Select at least one of the following
Status 3 Justification Form
Section IV
Exception for status 3
Status 3 Justification Form
Section IV
This exception request is specifically related to a device recall
Status 3 Justification Form
Section IV
Clinical Narrative






OMB No. 0915-0157; Expiration Date: XX/XX/20XX

PUBLIC BURDEN STATEMENT:

The private, non-profit Organ Procurement and Transplantation Network (OPTN) collects this information in order to perform the following OPTN functions: to assess whether applicants meet OPTN Bylaw requirements for membership in the OPTN; and to monitor compliance of member organizations with OPTN Obligations. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. The OMB control number for this information collection is 0915-0157 and it is valid until XX/XX/202X. This information collection is required to obtain or retain a benefit per 42 CFR §121.11(b)(2). All data collected will be subject to Privacy Act protection (Privacy Act System of Records #09-15-0055). Data collected by the private non-profit OPTN also are well protected by a number of the Contractor’s security features. The Contractor’s security system meets or exceeds the requirements as prescribed by OMB Circular A-130, Appendix III, Security of Federal Automated Information Systems, and the Departments Automated Information Systems Security Program Handbook. The public reporting burden for this collection of information is estimated to average 0.27 hours per response, including the time for reviewing instructions, searching existing data sources, and completing and reviewing the collection of information. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden, to HRSA Information Collection Clearance Officer, 5600 Fishers Lane, Room 14N39, Rockville, Maryland, 20857 or paperwork@hrsa.gov.
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