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Review Article LongTerm Ventricular Assist Devices Main Complications in Contemporary Clinical Practice Dayanna Machado Pires Lemos,1,2 Gustavo Paes Silvano,1 Kely Regina da Luz,1 Marco Aurlio Lumertz
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How to fill out long-term ventricular assist devices

01
Gather all necessary medical records and documentation.
02
Conduct a thorough evaluation of the patient's cardiac function and overall health.
03
Discuss the patient's eligibility for a long-term ventricular assist device with a multidisciplinary team.
04
Choose the appropriate type of ventricular assist device based on the patient's specific needs.
05
Prepare the patient for surgery, including pre-operative assessments and consent.
06
Perform the surgical implantation of the ventricular assist device.
07
Monitor the patient closely during the recovery process, managing any complications.
08
Educate the patient and family on device management and the importance of follow-up care.

Who needs long-term ventricular assist devices?

01
Patients with severe heart failure who are not candidates for heart transplantation.
02
Individuals experiencing significant symptoms of heart failure, such as shortness of breath and fatigue.
03
Patients who require support for the heart's pumping function.
04
Those who have a poor quality of life due to heart-related issues.
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Long-term ventricular assist devices are mechanical pumps that are used to support heart function and blood flow in individuals with weakened hearts, particularly in patients with advanced heart failure.
Healthcare providers and institutions that implant or manage long-term ventricular assist devices for patients are required to file relevant documentation and reports.
To fill out the necessary documentation for long-term ventricular assist devices, healthcare providers should follow the specific guidelines set by health authorities, ensuring all required patient information, device details, and procedural data are accurately recorded.
The purpose of long-term ventricular assist devices is to improve the patient's quality of life by maintaining adequate blood circulation and organ perfusion in patients with severe heart failure, possibly acting as a bridge to heart transplantation or as a long-term therapy.
The information that must be reported includes patient demographics, device type and model, implantation date, monitoring data, adverse events, and any other relevant clinical information pertaining to the patient's condition and device performance.
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