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    What to Expect with In-Center Hemodialysis

    Starting a hemodialysis routine.

    As with anything new, being prepared and understanding what’s involved with dialysis can help ease your mind. Being well informed will make the process go as smoothly as possible with your care team.


    Getting in the flow of a new routine

    You'll also be establishing a new routine in your life. On 3 days of every week, you’ll be going to a dialysis center for a treatment session, lasting 3 to 5 hours for daytime hemodialysis or around 8 hours for nocturnal (nighttime) hemodialysis. Embrace the time. Make it as relaxing or as productive as you wish. You may even make new friends there.


    First things first: planning ahead

    Before in-center hemodialysis treatments can begin, you will need a simple surgical procedure that creates a dialysis access site under your skin. An access site allows blood to flow from your artery through a tube to the dialysis machine for filtering and clean blood to flow back to your body through another tube to your vein.

    There are 3 types of hemodialysis access options: fistula, graft or hemodialysis catheter. While each type has its own benefits, speak to your doctor about which is best for you. 

    If you know you will need a fistula, you should be aware that it will be approximately 2 to 3 months before it can be used for your dialysis treatment. If you don’t plan ahead, you will need a hemodialysis catheter—a temporary access site—in order to receive treatment.


    Getting ready for your hemodialysis treatment

    A few minutes before your treatment session, a few simple but important steps are taken to monitor your health and help provide an effective outcome.

    Checking weight and fluid levels.

    Your weight is checked to see how much excess fluid you’re retaining and how much needs to be removed by dialysis.

    Wash your hands and access site.

    You wash your hands and you or your technician washes your access site to help prevent infection.

    Take vital signs, blood pressure and pulse.

    Your vital signs, including blood pressure and pulse, are taken.

    Check the access site and draw blood.

    Your access site is checked and prepared for dialysis. Small samples of blood may also be drawn from your access site for testing.

    Connect the access site to the hemodialysis machine.

    Finally, your access site will be connected to the tubing on the hemodialysis machine and the treatment will begin.

    Find a Fresenius Hemodialysis Center
    Find a dialysis center near you
    Use our Center Locator to find a convenient location or get directions.
    Find a center
    Planning your access surgery
    Once you and your doctor have decided on an access type, you'll want to schedule your surgery. Azura Vascular Care, an affiliate of Fresenius Kidney Care, offers minimally invasive, outpatient dialysis access surgery.
    Find a location near you
    Caring for your access
    Your access will work best when it's kept healthy. Once you get your access, it's important to make proper care part of your daily routine.
    Learn more

    Receiving treatment

    Program the hemodialysis machine and set the timer.

    After you’ve been prepped, a trained team member will program the hemodialysis machine with your fluid goal, turn on the pump and set the timer.

    Regular monitoring during hemodialysis treament.

    You will be regularly monitored during your treatment to make sure that you are tolerating it well and your treatment is working.

    Relax while the hemodialysis machine does the work.

    While the hemodialysis machine does all the work, you can sit back and relax. If you wish, you can also read, watch TV, work on your computer, listen to music or do something else that you enjoy. If you are dialyzing at night, you may wish to simply go to sleep.

    Socialize and make friends during treatment.

    You may also find that you enjoy talking with other people being treated. You may even make a new friend and discover ways to support and encourage each other.


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    Did you know?
    During a typical dialysis treatment, only a pint of blood is outside of your body being cleaned and returned at any time. One pint is the same amount of blood you give during a donation.

    Completing your treatment session

    Disconnecting from hemodialysis after treatment.

    After your treatment session is completed, a timer will sound and a trained team member will disconnect you from the machine.

    Removing needles and evaluating the access site.

    Your needles are removed or your catheter is capped and the access site is evaluated. A pressure dressing may be applied to prevent bleeding.

    Vital signs and fluid are checked.

    Your vital signs are rechecked and your weight is recorded after your treatment to see how much liquid has been removed.

    Resuming your normal activities.

    If your vital signs are stable and you’re feeling well, you’re free to go home and resume your normal activities.


    5 things I wish I knew about hemodialysis before I started

    1. You have options for doing hemodialysis. Even if you’ve started on in-center hemodialysis, you can switch to home hemodialysis if it’s a better fit for your lifestyle. Or you may be able to do overnight (nocturnal) dialysis at your center if you work, go to school or have busy days.
    2. You can travel and keep up with treatments. Contact Fresenius Kidney Care Patient Travel Services at 1-866-434-2597 (option 1) to arrange treatment at a Fresenius Kidney Care center near your destination.
    3. Going to the center can be social. One upside to frequent center visits is getting to know people who can relate to your experience.
    4. You can feel chilly during treatment. The dialysis process can make some people feel cold. Treatment rooms are also temperature controlled and may be cooler than you’re used to. Dress in loose layers or bring along a blanket—you’ll just need to keep everything clear of your access site.
    5. Dialysis treatment can be useful “me time.” Take the opportunity to listen to your favorite music, read a book, write a card, pay bills or shop online.

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    Maximizing benefits, minimizing hemodialysis side effects

    Get the most out of your hemodialysis session.

    Getting the most out of dialysis sessions

    • Completing your treatment. It’s important to complete your entire treatment session to get the full benefits. Stopping even 5 minutes early can affect your health. You may not feel the effects of shortened or missed treatments immediately, but not getting enough dialysis allows waste to accumulate in your body over time—and cause serious health complications.
    • Machine settings. The pump speed at which your blood flows is also important and will require careful adjustment by your care team to provide the most effective treatment. Slower pump speeds are easier on your body, they don’t filter as much blood. If the speed is too slow, you may not have enough toxins removed. If the speed is too fast, it may force blood through your veins with too much pressure and damage your veins and access site.
    Monitoring hemodialysis side effects.

    Monitoring hemodialysis side effects

    • Nausea or cramping. You may experience common dialysis-related symptoms such as abdominal cramps, nausea or other hemodialysis side effects. If you’re feeling uncomfortable at any time, speak up immediately and let your care team know. They may need to check your access site or adjust the speed of your pump, your medication or hemodialysis fluids. They may also give you something to help you feel better.
    • Feeling cold. You will also notice that the room may seem cool. This is because cool room temperatures help decrease humidity, which prevents bacterial growth that can lead to infection. If cool temperatures are uncomfortable for you, you may want to bring a sweater or blanket.
    • Fatigue. You may feel very tired during the first several months of treatment and you will need someone to drive you to and from each of your appointments. You may wish to ask a family member or friend to drive you. Or speak with your social worker about low-cost or free resources for transportation. When you feel well enough, you may be able to drive yourself or take public or private transportation on your own.
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