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Good Handwashing
Handwashing is important for staff and visitors and it is also very
important for the patient. You can never wash your hands too much! Hands
should be washed after going in and out of your child's room, after going
to the bathroom, and before eating. (For boys who use the urinal at night,
it is sometimes helpful to leave washcloths or some type of handiwipes
at the bedside). Please instruct visitors to also wash their hands when
entering and leaving your child's room.
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Protective Isolation, Air Filters and Masks
On admission, your child is placed on "protective isolation". This means
that they are at risk for developing infections and their exposure to
people who are ill should be minimal. Everyone entering your child's room
must wash their hands and wear a white cover gown (except nurses who wear
scrubs). Do not hesitate to remind someone to wash their hands or put
a gown on.
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Visitors should be screened. If they have any cold or flu symptoms, cold sores,
open sores, or recent exposures, they should not visit. Feel free to check with
your nurse if there is any question. If your visitor is a child, they must be
screened by a nurse. This is especially important because children may have
been exposed to contagious illnesses such as chicken pox or may have recently
received immunizations. In either case, they should not visit or be on the PBMT
unit.
The PBMT unit receives air that has passed through "hepa filters". The large
hepafilter units in the hallway and the portable room sized filters in each
room gives your child plenty of protection. The small filters in your child's
room should be on at all times and should always be set on speed "4". Your child
will remain in a filtered room during the transplant and immediate time after
transplant. When your child's counts have recovered, he/she may be moved to
another private room.
Even though the air is filtered, we still ask that your child wear a blue mask
when out of their room. Please change the mask if it gets moist or soiled and
always throw it away if it drops to the floor. We also ask that your child routinely
changes their mask two to three times a day. When off of the unit, a white,
heavier mask is required.
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Daily Bath or Shower
Your child must take a bath or shower every day. Baths
must be taken in a tub. No bed baths are permitted unless your child is
very ill. This is an important guideline as soaking in the tub or shower
has many benefits that you do not get from a bed bath. If you help your
child with their bath and dressing change, it may be completed anytime
during the day. If the nurse is to complete or assist with these cares,
they will be done on the day shift, preferably in the morning. Of course,
if your child does not need assistance and does these cares by themselves,
they can be completed at any time.
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If your child prefers to shower, make sure you clean their bottom area thoroughly.
If the bottom becomes sore, baths are preferred because the soaking helps to
clean and heal the bottom. Each child is prone to diarrhea and good bottom care
is important to prevent skin breakdown. Rectal sores may be treated by doing
a sitz bath two or three times a day. There are options available for creams
to apply to your child's bottom area and your nurse will be happy to help you
pick the best treatment for your child.
Skin Care
Skin care should be an important part of your child's daily routine. Total body
irradiation, chemotherapy, and the general dryness on the PBMT Unit will all
add to your child's dry skin. Even if dry skin has not been a problem in the
past, it is very likely to be now.
The key to skin care is beginning with a skin care routine right from the start.
You should use a mild soap and if you want, you can add bath oil to your child's
bath or rub it in during their shower. The bath water should not be too hot
as hot water is more drying. After the bath or shower, dry off by patting the
skin with a towel. While still slightly damp, apply lotion over all of your
child's body. Before radiation, applying lotion once a day is adequate. It is
best to apply the lotion after radiation is completed for the day. After radiation
is complete, start a routine of applying lotion twice a day. If you have any
questions on the lotion or soap that you are using, please ask your nurse.
Oral Care
Your child should do oral care four times a day. A soft toothbrush can be
used even if the platelet count is low. The only time that we ask that you not
use a toothbrush is if your child experiences any bleeding from their gums.
If there is any gum bleeding or irritation, we prefer that you use a toothette
or a very soft toothbrush for all mouth cares. Mouth care is very important
to prevent oral sores and infections. It is best for your child not to get behind
with mouth cares. This means that even if they do their first one at noon and
their second one at six, they still have two more that day. If the night nurse
comes on and finds that your child is behind, your child may be asked to get
up at midnight to do one. Remember, it is only being done to help. An antifungal
and antibacterial rinse will be ordered to accompany normal brushing (see procedure
below).
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If you are using a toothbrush:
- brush as usual
- rinse with sterile water
- swish with normal saline (salt water) and spit
- swish with an antifungal agent and swallow
- nothing to eat or drink for 20-30 minutes
- swish with peridex and spit
- nothing to eat or drink for 20 minutes
- A & D or vaseline to lips
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If using a toothette:
- swab all surfaces of mouth with toothettes soaked in normal saline
- if old enough, swish with normal saline
- swish with antifungal agent and swallow (for babies, swab medication into
mouth) making contact with all surfaces - do not just squirt it in with a
syringe. This is especially important if there is thrush along those hard-to-reach
areas of the gum line).
- A & D or vaseline to lips
Nystatin and clotrimazole are the two most common antifungal agents. Clotrimazole
slowly dissolves in your mouth or it can be crushed, mixed in water, and swished
and swallowed. If you choose to suck on the troche, move it around in the mouth
as it dissolves. It is best to suck on the troche until it is completely dissolved.
If this is not possible, it must be sucked on for 30 minutes before throwing
it away. Nystatin is a yellow liquid. You swish for 30-60 seconds and then swallow.
Peridex is an antibacterial mouth wash which is to be used twice a day. It
needs to be swished for
30-60 seconds and then spit out. Peridex can cause a temporary discoloration
or staining of the tongue and teeth on some people. If you notice any of this,
do not be concerned as it can be easily removed with a routine dental cleaning.
(For parents who swab peridex into their child's mouth with a toothette, peridex
is not harmful if swallowed).
Pediatric dentistry will see your child initially and is available for follow-up
visits as needed. They are often helpful when it comes to problems and finding
effective remedies.
Exercise
Exercise should be a part of your child's daily routine on the PBMT unit
and needs to be done at least three times a day. Younger children generally
do not have a problem in this area as they are usually up and in the playroom
or out riding bikes in the hallways. If your child is older, it is often harder
to make them get out of bed to exercise, especially if they are not feeling
well. We know it is hard, but cannot stress enough how important good exercise
is to your child as they go through the transplant process.
If your child is having trouble in this area, we will initiate an exercise
schedule for them, such as walking around the unit three times a day or riding
the exercise bike ten minutes twice a day. If your child chooses walking or
riding the stationary bike as their form of exercise, you may want to keep a
record of the progress your child makes (time, miles, tension, etc.). We like
to avoid the use of wheelchairs as much as possible. Physical therapy is always
available, and can help you set up some goals for your child's exercise. Let
your nurse know if at any time you would like your child to see a physical therapist.
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If there are times when your child feels too ill to geout of bed, physical
therapy will come and do bed exercises with them. Even when your child
feels the worst, we will still push them to get up and out of bed if at
all possible. Getting into a chair at least three times a day and doing
whatever activity or exercise you can, will be beneficial to them. Exercise
is important to keep the muscles toned and to help expand the lungs and
keep them free of infection.
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Another form of exercise specific to your lungs is the incentive spirometer.
This needs to be done (ten repetitions) at least four times a day (in addition
to your other exercise) and helps by fully expanding the lungs. Your nurse will
show you and your child how to properly use your incentive spirometer.
Physician Rounds
Two times a day, usually around 8:30 a.m. and 4:00 p.m., the physician and/or
physician assistants will be in to visit with you and your child. In the morning,
a complete assessment will be done on your child. Evening rounds are usually
to check in with you and see if your child has any needs. We like for parents
to be here for rounds. This is an excellent time for you and your child to talk
with the medical and nursing staff about your questions, comments, concerns
and needs. Please feel free to ask questions or express concerns at any time
with the PBMT staff.
Schedules
For the child undergoing a bone marrow transplant, there is a lot of stress.
Along with doing fun activities and talking with your child about their feelings,
it is important to develop a daily schedule to help your child cope. Children
usually handle stress better when they have a familiar routine to follow.
You and your child then know what is expected every day. A schedule also provides
clear direction for your child's daily activities. Working with your child to
develop a daily schedule also allows your child to feel control. Feeling like
they have a say in their day increases cooperation.
Daily tasks that must be completed, along with fun and rest times can be scheduled.
Allowing the child to decorate their schedule and the use of stickers as rewards
will help to make the schedule a fun activity.
Your primary nurse can assist you and your child to develop a daily schedule
that will help make the stress of being hospitalized a little easier if you
are interested.
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