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Suspending DR PLD7300F

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Suspending DR PLD7300F is a critical care procedure using a Portable Left Ventricular Assist Device to support patients with severe heart failure. The device is surgically implanted, connected to the left ventricle, and activated to assist the heart’s pumping function. The patient’s condition and device function are closely monitored during the support period. Duration varies based on the patient’s response and may be used while awaiting heart transplant or recovery. Weaning off the device occurs when the heart function improves.

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    Suspending DR PLD7300F is a medical procedure used in critical care settings to provide temporary circulatory support for a patient in need of advanced life support. It involves the utilization of a specialized medical device known as the PLD7300F (Portable Left Ventricular Assist Device) to assist the heart’s pumping function.

    Description of Suspending DR PLD7300F Procedure:

    1. Indication: The procedure is typically indicated for patients with severe heart failure, cardiogenic shock, or other cardiac conditions that result in the heart’s inability to pump blood effectively. These patients may be experiencing life-threatening hemodynamic instability.
    2. Preparations: Before initiating the procedure, a thorough assessment of the patient’s medical history, cardiac condition, and overall health status is conducted. The medical team should ensure that the patient meets the criteria for PLD7300F support and that all necessary consents have been obtained.
    3. Anesthesia: The procedure usually requires the patient to be under general anesthesia to ensure comfort and minimize patient movement during the device placement.
    4. Access: The medical team gains access to the patient’s circulatory system by inserting appropriate vascular catheters into the large blood vessels, such as the femoral artery and femoral vein, or via a more central approach.
    5. Device Implantation: The PLD7300F is a compact, surgically implantable left ventricular assist device designed to provide circulatory support. It is connected to the heart’s left ventricle, which is responsible for pumping oxygenated blood to the rest of the body.
    6. Device Activation: Once the PLD7300F is properly implanted and connected, it is activated. The device starts assisting the patient’s heart by pumping blood from the left ventricle into the aorta, thereby enhancing overall cardiac output and perfusion to vital organs.
    7. Monitoring: Throughout the suspension period, the medical team closely monitors the patient’s hemodynamic parameters, vital signs, and device function. They also manage any potential complications that may arise during the procedure.
    8. Duration: The duration of PLD7300F support varies depending on the patient’s specific medical condition and their response to therapy. In some cases, the device may be used for a few days to weeks while awaiting heart transplant or for the heart to recover its function.
    9. Weaning: Once the patient’s cardiac function improves sufficiently, the medical team gradually weans them off the PLD7300F support. This process involves careful assessment of the patient’s condition and monitoring the heart’s ability to resume its pumping function effectively.

    It’s important to note that Suspending DR PLD7300F is a highly specialized procedure performed by skilled and experienced medical professionals in specialized cardiac care facilities. The decision to utilize this circulatory support device is made based on the patient’s individual medical needs and the recommendation of a multidisciplinary medical team.

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