Dialysis

Dialysis Vascular Access

Dialysis Vascular Access

Information on access options can be found at www.kidney.org, www.aakp.org, or www.esrd.ipro.org.

Aterio-venous Fistula (AVF)

The fistula is the gold standard for vascular access and should be considered first for every patient needing hemodialysis.  This type of access is placed in any of the body locations listed below, by a vascular surgeon.  It is a connection between an artery and a vein to create a large blood vessel to provide a high volume of blood flow so that your hemodialysis treatment will be efficient and effective.  It also allows for repeated needle insertions. Although you may have had a catheter placed for an immediate treatment, The Regional Dialysis Center supports the “Fistula First” program.

The “Buttonhole” technique and self cannulation are also part our program.  Please ask your nurse about these techniques and “Fistula First”.

Locations: Forearm, upper arm

Advantages: Lasts many years

                     Less chance of infection

                     Higher blood flow rates

                     Fewer complications                       

Graft

A graft is another access that is inserted by a vascular surgeon.  It a synthetic tube placed under the skin in any of the locations listed below.  It can be straight or in a loop.  This type also allows for needle insertions for high blood flow. 

Locations: Forearm, upper arm, thigh (deleted straight or loop here)

Advantages: Can be used two weeks after placement

                     For use when a fistula does not work

                     For patients with special health issues

Catheter (Perm-Cath)

This is a temporary access that is placed by doctors in our Special Procedures Unit.  A dialysis catheter is placed under the skin and into a large vein that leads to your heart.  It has two lumens, one to deliver blood from the patient to the filter and the other one returns blood from the filter to the patient. 

Locations: Neck (jugular vein), groin (femoral vein), or chest (subclavian vein) — should be avoided

Advantages:

Only used in an emergency or for temporary access                                            

 Can be used when other access types are maturing

Disadvantages:

Infection 

Clotting

Lower blood flow rates

Vessel damage

Designed for short-term use only

Care of Your Vascular Access

Proper care of your vascular access must be followed to ensure your safety and prevent infections. 

Post-Dialysis Fistula or Graft Care

When the needles are removed from the fistula, while wearing a glove, the patient holds pressure over the needle sites to stop the bleeding.

Pressure should be adequate to stop the bleeding but not stop the blood flow through the access.

Pressure should be held for at least 10-15 minutes and released gradually.

The sites will be covered with bandages, which should remain on the sites until the next day.

Occasionally, you may experience leaking from the venipuncture sites after dialysis. If bleeding occurs, apply direct pressure to the site.

It is recommended you carry some 4 x 4 bandages in your purse or car, and have some at home to enable you to hold pressure on the sites to stop the bleeding.

Pressure should be held just as it is done post dialysis.

Notify the physician or dialysis center if bleeding occurs at home.

Care of the Fistula or Graft at Home

It is important to keep the fistula clean. By keeping the skin in the area of your A-V fistula clean, you can substantially reduce the risk of infection. Wash your fistula daily with soap and water.

On a daily basis:

Check your fistula for signs of infection such as redness, swelling, soreness, or drainage.

Check your fistula for proper function, making sure you feel a pulse or thrill along the length of your fistula or vein to which your graft is attached. To do this, place your fingertips over your access.

Wash your fistula site. 

You may shower and bath normally.

Do not:

Restrict blood flow through your A-V access for long periods. Be careful when lifting and carrying objects that press against it.

Sleep on your A-V access.

Use your A-V access for the administration of any drug or medication without professional renal medical assistance.

Wear tight jewelry over your A-V access.

Allow lab draws or IV insertions in the arm of the A-V fistula.

Allow your blood pressure to be monitored using this arm.

When to call the doctor:

Absence of thrill (buzzing sensation) in arm.

Pain or swelling in arm.

When signs or symptoms of infection occur. I.e.: drainage, tenderness, redness, warm to touch.

If any substantial bleeding occurs from fistula at home.

Treatment of hematoma or clotted access

Hematoma

A hematoma is bruising of the skin around your fistula caused by blood leaking into the tissue. Ice the area for 24 hours 15 minutes on 15 minutes off. Apply moist, warm compresses after 24 hours. Check your access for thrill. 

Thrombosed Access (also called a clotted access)

Removal of clot in the fistula or graft is necessary before the access can be used for the purpose of dialysis. This is done in the Special Procedures Unit and must be done as soon as possible once the clotted access is noted. 

Care of the Perm-Cath at home 

Check the exit site for signs of infection, such as drainage, swelling, redness, and soreness.

Keep a dry dressing over the port ends.

You may shower with your physician’s okay.

Cover your dressing before showering using plastic wrap or baggies. You may also use catheter shields, which are available online. Ask your provider for more details.

If the bandage covering the catheter exit site becomes wet, replace it with a clean, dry one. 

When to call the doctor:

If drainage, pain, swelling or redness is noted around the catheter exit site.

If fever is more than 100 degrees.

If the catheter comes out at home, place direct pressure on the skin site with the palm of your hand or any clean towel or washcloth.

Do Not:

Pull or tug on the catheter.

Remove any sutures that are holding the catheter in place.  This must be done by the nephrologist.

Allow usage of the catheter by anyone for IV or lab draws. 

Remove any caps or unclamp any clamps on the catheter.

Treatment Options

The Dialysis Center at Faxton-St. Luke’s Healthcare provides care for those with chronic and acute renal failure. The center offers several treatment options, including outpatient hemodialysis, home hemodialysis, and peritoneal dialysis. Not all patients are candidates for each method. Treatment depends on the patient’s physical condition, emotional condition, and family. Options can be discussed with the patient’s nephrologist.

Hemodialysis

Hemodialysis is a process where a small amount of blood (just over a cup) is removed from the body and sent through an artificial kidney. The artificial kidney has a cellophane-like membrane, and is bathed in a solution called dialysate. The blood is cleansed of waste products and excess fluid. The blood is then returned to the patient. Dialysis is not only the removal of fluid, but also the removal of waste. This includes electrolytes, especially potassium, which, in excess, can cause cardiac arrhythmias. Hemodialysis is usually performed three times a week, for three to five hours at our outpatient hemodialysis center located at the Faxton Campus.

Home Hemodialysis

If a patient is physically stable and mentally fit, the patient and his or her partner can be trained for home dialysis. Training may take 3 to 5 weeks to complete. The patient and partner are responsible for all aspects of the treatment including water testing, insertion of needles or accessing a catheter, and monitoring vital signs and machine operation. For more information on home dialysis, contact your primary nurse. The physician has final approval on whether this treatment is right for you.  The Regional Dialysis Centers offers NxStage home hemodialysis. 

Peritoneal Dialysis

Peritoneal dialysis removes waste products and excess fluid from the blood, but in a way different from hemodialysis. A membrane that surrounds all of our organs is called a peritoneal membrane. This membrane acts like an artificial filter that filters out waste products and excess fluid. In peritoneal dialysis, a catheter is surgically placed in the abdomen and dialysate is instilled into the abdomen and left for a number of hours. After a prescribed amount of time, the dialysate is drained out of the abdomen. It is a slower dialysis method and must be done several times during the day, every day. Sterility is vital during peritoneal dialysis connections.

There are two types of home peritoneal dialysis:

CAPD (Continuous Ambulatory Peritoneal Dialysis) is a manual method of doing exchanges.  The patient connects a fill and drain bag to the catheter, performs the exchange, and disconnects the tubing from the catheter. Exchanges must be done four to five times per day during waking hours. Precautions must be taken to assure sterile connections to the catheter. 

CCPD (Continuous Cycling Peritoneal Dialysis) is a method of doing exchanges with a machine called a cycler. The patient connects his catheter to the cycler, at midday or late afternoon, which automatically drains and fills the abdomen once. The patient disconnects himself and is free until bedtime. At bedtime, the patient reconnects himself to the cycler and the cycler automatically drains and fills the abdomen four to five more times during the night while the patient sleeps eight to 10 hours. Sterility is vital during the dialysis connections.   

Ask your renal team for more information on these dialysis treatment options.

Transplantation

Renal transplantation is the placement of a kidney from another person (donor) into the patient with renal failure. It involves major, but low-risk, surgery. The donated kidney can perform all the functions that the patient’s damaged kidneys are unable to do. 

The patient with a functioning donated kidney no longer requires dialysis treatments, because the kidney works more effectively than dialysis. The patient who receives a transplant generally feels better and has more energy. Many restrictions are lifted after transplantation, including food and liquid restrictions.

A strict medication regimen must be adhered to prevent rejection of the transplanted kidney. However, if rejection does occur, the patient may have to return to dialysis.

Once your physician gives you medical approval, arrangements can be made with the transplant hospital for information and evaluation.

Any questions about these treatment options can be asked of your primary nurse or physician.

Nocturnal Dialysis

This is a type of hemodialysis where you receive your dialysis treatments while you are sleeping at night for 6-8 hours.  This can be done in dialysis center or at home via a monitoring system with a dialysis unit.  The initial requirements are the same as home dialysis.  Nocturnal dialysis is not currently offered at Faxton-St. Luke’s Healthcare.

No Treatment

Dialysis is your choice. You have the right to refuse dialysis, or there may come a time when you feel that dialysis is no longer an option and you want to discontinue your treatments. If this occurs, it is important to discuss your feelings with your loved ones and your health care team. Your doctor and primary nurse can advise you about the type of care you may need once a decision has been made. Your social worker is also available to make arrangements for end-of-life care. More information is available at www.kidney.org.

Dialysis Medication

Q.        Do you know why you get Aranesp?

A.        Normal functioning kidneys produce a hormone called erythropoietin, which tells the bone marrow to produce red blood cells. Red blood cells carry oxygen throughout the body.  Diseased or damaged kidneys do not produce as much erythropoietin so the bone marrow makes fewer new red blood cells, a condition called anemia.

Q.        What does anemia feel like?

A.        If you have anemia, you may feel weak, tired and may lack energy most of the time. Even mild exercise may bring on fatigue, difficulty breathing and sometimes chest pain. Although dialysis makes up for the loss of some kidney function, it cannot correct anemia.

Q.        What is Aranesp?

A.        Aranesp is a drug that works just like the erythropoietin produced by the body. Aranesp stimulates the bone marrow to produce red blood cells at a more normal level.

Q.        When is Aranesp given?

A.        Aranesp is given once a week at the end of your dialysis session into the blood tubing during the rinse back of your blood.

The amount of Aranesp you receive is based on a blood test called hemoglobin. You will continue to get monthly hemoglobin tests to see if you are staying within the target range. Adjustments will be made according to your results.

Venofer/ iron sucrose

Q.        Why do I get Iron?

A.        To make red blood cells, your body needs iron as well as Aranesp. Chronic kidney failure patients on dialysis have a special need for iron. This is because you lose a little blood (which contains iron) during hemodialysis treatments.

You may also have other problems that cause you to lose blood, or that make it difficult for your body to store or release iron.

Q.        When is Iron given?

A.        Lab tests are done every three months to check your iron levels.

Iron is given during dialysis.

Depending on your iron levels you will receive iron every treatment for 10 treatments in a row and then once every two weeks or you may start out getting iron once every two weeks.

Hectoral/ doxercalciferol

Q.        What is doxercalciferol?

A.        Doxercalciferol is a form of vitamin D hormone replacement therapy.

Q.        Why do you need doxercalciferol?

A.       Kidneys are responsible for normal calcium balance. Normal calcium balance helps make bones strong and keeps them healthy. The healthy kidney makes a special form of Vitamin D called calcitriol.

When you have kidney disease, your kidneys stop making calcitriol. Without calcitriol, you cannot absorb enough calcium from your diet. The body begins to “rob” calcium from your bones. This makes your bones grow weak.

Also, without calcitriol, the glands in your neck (parathyroid glands) will make too much PTH- parathyroid hormone; this will cause even more calcium to be taken from your bones and increases bone disease.

If the PTH is not controlled, your doctor’s only choice may be to recommend that your parathyroid glands be surgically removed.

Doxercalciferol is given to restore PTH to safe levels and normalize calcium levels.

Q.        When is Doxercalciferol given?

A.        Lab tests are done every three months to determine how much doxercalciferol you require. It is administered every treatment at the end of your dialysis session into the blood tubing during the rinse back of your blood.

Helpful Resources

Helpful Resources

www.kidneyschool.org

A site for patients to take an active role in their health. Educational modules must be downloaded.

www.kidney.org

The official site of the National Kidney Foundation. It contains a wealth of information for patients and their families. 

www.aakp.org

The American Association for Kidney Patients is a comprehensive site for information.  There is a fee for joining the society. 

www.nxstage.com

An informative site for prospective home hemodialysis patients.

www.kidneyoptions.com

An informative site supported by Fresenius for patient education on options for dialysis and free information packets.

www.ultracare-dialysis.com

A site supported by Fresenius for information about dialysis units for travel, treatment options, education programs, patient information.

www.Davita.com

This site is a renal diet helper.  It supplies kidney friendly recipes.

Dialysis Appointments

Dialysis Appointments

What should I know before I get there on the first day?

Please arrive no sooner than 10 minutes prior to your appointment time. All appointments are carefully scheduled, and we are unable to accommodate you earlier than your prearranged time.

Please report to the waiting room rather than walking directly to the unit.

We apologize if there are delays in starting your treatment. Possible reasons may include equipment problems, staffing issues, or medical problems with other patients. Our top priority is the safe treatment of every patient in our care.

Treatments are scheduled three times per week for three to five hours, as prescribed by your nephrologist. Once you are given a regular schedule, on occasion, there may be circumstances that require us to ask you to change your dialysis time. 

If you wish to have a different dialysis schedule or want to go to a satellite unit, please notify your renal team. Changes are made based on your place on the waiting list and when your requested spot in the unit or schedule becomes available.

To ensure fairness to all patients who are treated at the center, we have a policy in place for patients who chronically arrive late for appointments, sign off treatments early (AMA), or do not show up for their appointments. We encourage compliance and give patients who abide by the rules a more preferred schedule.

What if I can’t make my appointment?

If for some reason you cannot make your appointment, please call 315-624-5660. The charge nurse may be able to reschedule you if time allows.

What should I expect at my appointment each day or week?

  1. Our staff will assist you into the unit at your scheduled time.
  2. You will be weighed on the scale while standing, while in your wheelchair, or while in the Hoyer lift. This weight determines how much fluid you have gained since your last treatment.
  3. You will be brought to your seat for your treatment.
  4. Your nurse will verify your identity by confirming your name and date of birth at every treatment.  
  5. Once in your seat, a nurse will take your temperature, blood pressure, and heart rate, and will examine you for signs of fluid overload, such as edema or shortness of breath. He or she will listen to your heart and lungs, and look at your vascular access for any signs or symptoms of infection or malfunction. This is the time to tell your nurse of any problems or complications you may be having or if you have had a change in medications. It is recommended that you carry an updated list of medications with you at all times. 
  6. The nurse will set your machine according to your doctor’s orders. 
  7. Your nurse will be wearing personal protective equipment for safety for example, a gown, gloves, mask, goggles or face shield. 
  8. Your nurse will prepare your vascular access by cleaning your fistula or your dialysis catheter. This prevents bacteria from entering your bloodstream and causing a possible infection. If using a fistula, the nurse will insert two needles into it. The purpose of the vascular access is to have a way to remove blood from your body and return it in high volumes.
  9. Once your dialysis access and the dialysis machine are ready, the nurse will then “connect” you to the machine using two lines. Labs that need to be drawn are taken before the connection to the machine is made. The access line pulls the “dirty” blood from your body, and the venous, or return line, pushes the “clean” blood back into your body. Approximately half a pint of blood is removed and returned to your body per minute.
  10. While on the dialysis machine, blood is continually being pulled from your body, traveling through the dialyzer (filter), which removes toxins and extra fluid. This is done by the processes of diffusion, osmosis, and ultrafiltration. The blood is then returned to your body.
  11. To prevent your blood from clotting in the dialyzer or blood tubings, Heparin is given during your treatment. 
  12. You are closely monitored by nursing staff throughout your treatment. You can expect to have your blood pressure taken every 30 minutes to make sure it is not too high or too low. 
  13. While receiving treatment, you may hear machine alarms. These alarms alert the staff of any potential problems and are quickly responded to and resolved. 
  14. Remain in a reclined position with your feet elevated while receiving treatment. This prevents your blood pressure from falling too low.
  15. If you have needles in place, please hold that part of your body still to prevent a needle from being dislodged.
  16. If at any time you do not feel well, please alert the staff. This includes nausea, muscle cramps, and dizziness.
  17. Report any pain using the Pain Scale 0-10 as a measurement. (Please note: The Pain Scale is located in the back of this guide for your reference.) 
  18. During each month of dialysis, expect to have blood work drawn, your feet and/or stumps checked for vascular problems, and a monthly education topic presented to you. You will also be asked about your medications to make sure your medication list is up to date.
  19. Once your treatment is completed, your blood will be returned to your body. Any post treatment lab work will be drawn before needles are removed or your dialysis catheter is closed.
  20. If you are patient holding your needle sites after they are removed, for infection control purposes, you will need to wear a glove. 
  21. Vitals will again be taken before you go home (this includes blood pressure, heart rate, temperature, and weight). Be sure to rest a few minutes before getting out of your chair if you feel lightheaded or weak.
  22. Every patient, before leaving the unit, must wash their hands, use the hand sanitizer or hand wipes provided by your nurse.  This is for your protection and for others.
  23. Remember: Watch your fluid and sodium consumption in between dialysis treatments. It is important to take good care of your body to receive the most from your dialysis treatments.

Who Will Be Caring For Me?

Who Will Be Caring For Me?

Nephrologist

Chances are good that you already have a nephrologist assigned to you. If you were admitted to the hospital, a consult was made with a nephrologist who directed your care. That same nephrologist will continue with your care, making rounds at the dialysis units. You may also have appointments at your nephrologist’s office. The nephrologist prescribes the orders for your dialysis treatments and is the only one who can make any changes. Some nephrologists have nurse practitioners who make rounds, and any of your questions for the physician can be discussed with the nurse practitioner.

Primary Nurse

Each patient is assigned a primary nurse who will oversee the patient’s treatment and plans of care. Your primary nurse doesn’t necessarily provide you with your treatment each time you have dialysis; an associate nurse may care for you. As mentioned previously, labs, education, foot checks, and medication reconciliation are done on a monthly basis and overseen by your primary nurse. Any questions you may have about your treatment can be directed to your primary nurse.

Social Worker

You will be assigned a primary social worker who can provide assistance to you and your family in adjusting to kidney disease and helping you maintain an optimal quality of life. The social worker can assist you with changes you experience in the home, workplace, and community. He or she can help you plan a treatment schedule that fits your lifestyle, help schedule travel plans, and identify supportive resources to meet your needs. The social worker is available to help with any other issues or concerns as they arise, so please feel free to contact them.

Dieticians

Part of your responsibility during dialysis involves making adjustments in your eating habits to prevent a dangerous build up of toxins. A dietitian will work with you to individualize your nutrition care plan, educate you and your family about diet changes, and review your monthly lab work with you. Your dietitian will help you adjust to your diet while addressing your individual nutritional needs.

Care Attendants

Care attendants are assigned to the same area in the center daily. They are attentive to the needs of the patients and nurses. Any questions asked of them will be directed to the nurse.

Other Providers

There are many people who work at the dialysis center to ensure its smooth operation. They are secretaries, biomedical technicians, a financial coordinator, and unit managers. 

Dialysis Bio-Med Team

Our dialysis bio-med team is comprised of three certified dialysis technicians with more than 30 years combined technical experience, as well as a certified water technician.  Their mission is to ensure that all dialysis-related equipment is operating optimally at all times to provide our patients the best care available.

Your safety and well-being are of the utmost importance. Our team of dedicated professionals works diligently to ensure that the stringent standards of the Department of Health, as well as our organization, are always met. Some of the steps taken to ensure adherence to these guidelines include detailed inspections, evaluations and any equipment repairs required. 

 

About Relationship-Based Care at Faxton St. Luke's

About Relationship-Based Care

What is Relationship-Based Care (RBC)?

With RBC, nursing is just one part of the healthcare delivery picture. It takes an entire organization to care for you. Nursing plays a significant role in your care and recovery, but each and every employee has a piece in creating a positive experience for you.

Relationship-Based Care (RBC) was adopted by FSLH following the consolidation of Faxton Hospital and St. Luke’s-Memorial Hospital in the fall of 2005. FSLH partnered with Creative Health Care Management to build and sustain this model of patient care which has helped FSLH become a healthcare organization that provides a positive, caring and healing experience for you and your family. It has been instrumental in guiding our employees and creating exceptional teamwork.

What are the principles of RBC?

  1. Responsibility for relationship and decision making - a registered nurse manages your care from admission to discharge
  2. Continuity of care through work allocation and patient assignment
  3. Communication
  4. Management
  5. Process improvements
  6. Providing a caring and healing environment of care

Every department is represented at the table and has a voice in making decisions about how care and service are provided in their own area. Employees in our 60 units and departments continually look at processes and procedures and ask, “How can we do this even better and make sure that the patient and their family are always our central focus?”

How do employees have a voice?

Each of FSLH’s 60 departments has a Unit Practice Council (UPC). The UPC is a small group, usually 8-10 people, who meet regularly to discuss issues/challenges that have arisen and work on solutions to improve them. Unit Practice Councils are comprised of individuals who are selected by their peers and accept the responsibility, authority and accountability to represent the staff on the unit. UPC members focus on implementation of the RBC principles, always putting the you and your family at the center of all they do.

Once a month, all 60 UPCs send a representative to a meeting where the details of creating the best possible patient experiences are discussed and coordinated among all the members.

Working together, UPCs have helped to streamline patient transport, address dietary issues and expedite linen delivery, to name a few. They have also improved employee satisfaction, which we believe is integral to delivering quality healthcare – happy employees lead to happy patients.

Are other healthcare organizations doing this?

Organizations that preceded Faxton St. Luke’s Healthcare with implementation of the Relationship-Based Care model only involved nursing. FSLH was the first in the nation to roll out RBC system-wide.

In July, 2009, Faxton St. Luke’s Healthcare was on the national stage as our organization took part in the National Relationship-Based Care Symposium held at the Turning Stone Resort. The symposium, hosted by Creative Health Care Management, showcased our employees and the great strides FSLH has made on our RBC journey. Leaders in diverse roles at all levels of healthcare organizations from across the United States attended and several toured FSLH to speak with staff and further examine our success.

Since the symposium, healthcare organizations across the country have contacted FSLH to learn how we were able to engage the entire organization, every employee in every department. As part of the Keith A. Fenstemacher Center for Continuous Learning, we have begun a formal two-day program for organizations to attend to learn first-hand about our road to success.

Our journey isn’t over; we are still working to further improve the patient and family experience. It isn’t always easy, but it’s what we are passionate about. The commitment of our leadership and the hard work and dedication of our more than 3,000 employees have made this exciting transformation possible. As we continue our journey, we are reminded about the two things that make Faxton-St. Luke’s Healthcare special – It’s the people. It’s the care.

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