Kidney Transplantation
About Kidney Living Donors & Tranplantation

Another option for transplant is the living related and living unrelated process. This is when someone you have a relationship with (either genetically related, or unrelated) donates one of their kidneys to you for transplant.

This is a very safe procedure for the donors. They can live a long, happy, and healthy life with one kidney. Donors are screened and tested very thoroughly before donation to ensure that removing a kidney will not affect their health in any way.

There are several advantages to receiving a kidney from a living donor.

 

  1. There is no need to wait for a cadaveric kidney to become available (most living transplants take place  four to six months after the evaluation process begins).
  2. The kidney usually begins to work immediately, even in the operating room. There is a very low  occurrence of ATN (acute tubular nephrosis) in living transplants. A cadaveric kidney may not work right  away for several reasons. This is known as ATN.
  3. There are fewer episodes of rejection. As a result, living donated kidneys tend to last longer.
  4. There is a need for less immunosuppressive drugs, which therefore minimizes the possible side effects.
  5. Living related transplants can be scheduled. This allows both you and the donor to plan for absences from  work, childcare, and other social concerns.

 

To do

Physicians

Manager

  • Gail Frankle, RN, MEd, CPTC

Coordinators

  • Amanda Donovan, RN, BSN
  • Colleen Farrell, RN, CCTC
  • Shannon Prizniak, RN
  • Sandra Ryan, RN
  • Nancy Sabb, RN, BSN
  • Mary Ann Smith, RN, BSN, CCTC

Financial Counselor

  • Faith Baker

Staff Assistants

  • Jessica Giansanti
  • Tanya Gogets, MOA
  • Carol Hershey
  • Martha Kleinfelter
  • Monica Progin

Social Workers

  • Velma Carter-Dryer, MSW, ACSW
  • Hilary Hoover
  • Cynthia T. Royer, MS, BS

Pharmacist

  • Tracy M. Valania, Pharm. D.

Nutritionist

  • Karen E. Smith, RD, CDE

To do

Who can I talk to if I’m not sure a transplant is right for me?

Talk with your nephrologist about the transplantation process. To set up a clinic appointment to learn more about transplantation, call our office at 717-531-3716. Clinic meetings are scheduled every Monday and Thursday morning from 7:30 a.m. to 12:00 p.m..

After an appointment is scheduled, call the transplant office if any changes in your schedule occur that would prohibit you from keeping your appointment. You may reschedule your appointment at this time. A packet of information will be sent out to you. Please fill in the information requested, and return it to our office as soon as possible.

What do I do if I have a person(s) to donate a kidney?

Have your donor(s) call our office prior to your clinic appointment. A secretary will screen the donor(s) with a few questions.

  • If at this time the donor(s) does NOT know his/her blood type, we will mail them a physician’s order to have their blood type tested at a local laboratory. The laboratory should fax the results to us at 717-531-3717. (The donor(s) blood type must be compatible.)
  • If at this time your donor DOES know his/her blood type, they need to bring written documentation of their blood type to our clinic meeting. This can be a blood donor’s card, or it may be a note from their primary care physician.

How many donors can I bring with me?

You can bring as many people with you as would like, although we will only work up two people at a time. They must have documentation of their blood type with them.

What do I need to do after the clinic meeting?

A letter will be sent out to each patient stating whether or not they are considered a candidate for transplantation, along with a list of tests that need to be completed for listing. This letter will also be sent to your nephrologist, the dialysis unit and your primary care physician.

How do I get all these tests completed?

Your nephrologist’s office can schedule all the tests for you, if you are not currently on dialysis. If you are on dialysis, the staff can usually help schedule tests.

NOTE: By patient request - the patient can have all the testing completed at Penn State Milton S. Hershey Medical Center. Our office can schedule the tests for you.

When will I be put on the list?

When all testing is completed and the results are faxed to our office, the transplant physician will review your records. If at this time, no further testing is indicated, you will be put on the list. One of the pre-transplant coordinators will call you at home to let you know when you are listed. You will also receive a letter in the mail. You are NOT listed until you are called by one of our staff, or you receive this letter.

Do I need to do anything after I am listed for transplantation?

You will receive a second letter stating whether you need annual testing to remain active on the transplant list. Also, a blood sample will be taken at the beginning of each month for your physician’s office or dialysis unit. It will be sent to our lab so we may have a current sample on each patient. This allows us to start testing your compatibility with a potential donor before you arrive at the hospital.

 

Daily Tasks

You will be asked to monitor your weight on a daily basis and your blood pressure and temperature twice a day and record them on the chart that will be included in your patient teaching manual.

 

  • Take your temperature in the morning and in the evening. Call the transplant team if your temperature rises above 100 degrees F. Do not take medication to lower your temperature unless instructed to do so by your transplant physician.
  • Check your weight every morning before breakfast, after you have gone to the bathroom. An increase in weight may mean that you are retaining fluids, or that you may need to control your calories.
  • Take your blood pressure every morning and evening. If the top number is > 160 or if the bottom number is > 100 report it to the transplant team.

 

Potential Complications

Rejection

The biggest problem facing all transplant patients is the possibility of rejection. Rejection is the body's attempt to get rid of a foreign substance, in this case your new kidney. There are several kinds of rejection, and they can be a common and life-long issue.

 

  • Hyperacute - This severe form of rejection happens within minutes or hours after transplant surgery. The new kidney must then be taken out. This form of rejection is very rare.
  • Acute - This is the most common type of rejection, and while it can happen anytime, it more frequently occurs during the first six months after transplant.
  • Chronic - This type of rejection can happen at any time, including years after the transplant.

 

A common cause of (chronic) late rejection is not taking your medication, skipping days, or taking the wrong dosage. The medicines that you take will help lessen the number or severity of the rejection episodes, but may not completely prevent them. Most rejections that happen shortly after surgery can be treated medically. If you have rejection symptoms, call the transplant office. The quicker you receive treatment, the more successful the treatment is likely to be.

Some of the signs of rejection are:

 

  • fever above 100oF
  • swelling or tenderness over the new kidney
  • flu-like feelings
  • weight gain of 4 or more pounds overnight
  • decrease in urine output
  • elevated blood pressure

 

It is also important to remember that you may be experiencing rejection without any obvious signs or symptoms. That is why it is so important to have your blood tested on a regular basis and to follow the schedule outlined under the "Daily Medical Tasks" tab. If it is felt that you are having rejection you may have to have your kidney biopsied. This can be done on an outpatient basis. If it is determined that you are in rejection you may need your steroid doses increased. At the end of three days, if your BUN and Creatinine have not decreased, you may have to have IV medication to reverse the rejection and will need to be admitted to the hospital.

Infection

The medications you take to prevent rejection will also place you at greater risk for infection, as they suppress your immune system. Common areas for infection are your lungs, bladder, or the incision site. You will be on medication for the first six months to help decrease your risk of getting an infection. Be sure to tell your family that family members who are ill should not come to visit.

Notify the transplant coordinator

  • if you have a cough that lasts longer than 3 days
  • if you get pain in your chest or short of breath with the cough, or if you cough up anything green or yellow
  • if you have any pain or burning when you urinate
  • if you have any blood or blood clots in your urine or the urine becomes cloudy or foul smelling
  • if you notice your incision getting red, swollen, or secreting pus or fluids

Delayed Graft Function

The functioning of your kidney transplant may be delayed, causing a need for dialysis or longer hospital stay until the kidney "wakes up." Delayed function may last from several days to several weeks.

Diabetes

Some of the immunosuppression medications you take may cause diabetes. Diabetes is an increased level of glucose (sugar) in your blood. Signs of diabetes may include being thirstier, urinating more often, having blurred vision and being confused. Call your transplant coordinator if you have any of these signs. Your blood glucose levels will be monitored for the first year to help detect any problems early.

If you should develop diabetes, you will be given teaching on how to deal with this problem. In some cases, diet, weight loss and exercise can control it. Some people need oral hypoglycemic medications or insulin to help control their diabetes.

High Blood Pressure

High blood pressure is also a common side effect of some of the medications you take. You may need another medication to control your blood pressure. Following your vital signs schedule carefully will help detect this problem and allow early treatment to avoid complications from high blood pressure. Call your transplant coordinator if your blood pressure consistently reads higher than 160/100.

You will be taking medication for the rest of your life in order to prevent your body from rejecting your new kidney. While hospitalized, you will be told what medicines to take, what each medicine does, and common side effects of each medicine by the pharmacist, your nurses, and coordinator. You must become familiar with the names, dosage, and recording of all your medications. The number and dosage of the medicines will be lowered as you improve. Never stop taking a medicine without talking to the transplant team.

Also, you must never take prescriptions from your family doctor or over-the-counter medicines, without first talking to the transplant team. This includes common medications such as aspirin or Tylenol. Many drugs cause serious side effects in patients taking anti-rejection medications. Telephone the transplant program before taking new medicines, even on an emergency basis and even if ordered by a physician in an emergency room. Call your transplant coordinator FIRST!