| Congestive
Heart Failure
This booklet has been written to answer questions that
many patients and family members ask about their care
during their hospital stay. It will explain the experiences
you will have while you are here. Using this as a guide,
your care will be adapted to your needs. When being
treated for just Congestive Heart Failure, your length
of stay may be about 4 days. You may stay a shorter
or longer time, depending on many factors.
Remember, this is a guide Specific care and timing will
be adjusted to you.
Guide to MEETINGS in the Hospital
Someone from Respiratory Care will come to your room
to talk about your breathing and evaluate your oxygen
needs. They will see you every day.
A Nutrition Supervisor or Dietician will come to talk
with you about your food preferences and patterns, answer
questions you may have, and help you learn to about
low sodium foods.
A Pharmacist will talk with you about your medications,
how to take each one, and what to expect from each one.
A Discharge Planning nurse will help you with any help
you may need after you leave the hospital.
The second day you are here you will have a visit by
a Physical Therapist to evaluate any needs you may have.
He or she will work with you to increase activity without
making your symptoms worse, and will also help you to
set up a home exercise program.
Guide to ACTIVITY in the Hospital
How much you do will depend on your comfort with breathing
and your oxygen level as measured by the oximeter.
The physical therapist will work with you on learning
to balance your activity and rest. When able, you will
start by walking twice on the unit as well as to the
bathroom on the first day.
On the 2nd day you will walk 2-3 times and practice
stepping on and off a 6 inch step. Someone from physical
therapy will work with you on a home exercise plan.
Your main goal the last two days you are here will be
to prepare to go home.
Guide to NUTRITION in the Hospital
Your diet will depend on your condition. You may start
on liquids if you are very sort of breath, and then
advance to solid foods. You will be encouraged to eat
6 small meals per day. A nurse or nutrition supervisor
can help you make out the menu for each day, using a
2gram sodium limit. The sodium restriction will help
prevent your body from retaining excess fluid. Your
doctor may also want to limit how much fluid you drink.
Guide to TREATMENTS in the Hospital
IV
Fluids and medicines may be given to you through an
intravenous catheter, or IV. The IV tubing may be disconnected
so that you can move around more freely. The IV catheter
will be removed the day you go home.
Intake & Output
While you are here the nurse will measure the amount
of fluids you drink and will also measure your urine.
You may have a Foley catheter put into your bladder
to drain your urine. If you have a Foley catheter, it
will be removed and we will make sure you urinate before
you go home.
Vital signs
You will be weighed you arrive and every day in the
early morning. Your temperature, blood pressure, pulse,
and rate of breathing will be checked every 4 to 8 hours
or more often if needed. The doctor and nurse will listen
to your heart and lungs every day. You may wear a portable
telemetry unit so that your heart rhythm can be watched
as you go about your activities.
Oximeter
A clip or wrap will be placed on your finger or earlobe
to check the oxygen level in your blood. This will be
checked regularly to help decide your oxygen needs.
It will help determine if you need oxygen and how much.
This will be removed before you go home.
Guide to TESTS in the hospital
Lab tests will be ordered by your doctor. A laboratory
technician will draw blood for some of these tests.
The first day you are here, your nurse will send a urine
sample to the lab. You will also have a chest xray,
electrocardiogram (EKG), and perhaps an echocardiogram
the first day.
You will probably have more lab tests, an EKG and chest
xray the 2nd and 3rd days you are here.
Guide to MEDICINE in the Hospital
You will be given a diuretic to help your body eliminate
extra fluids, and medicines to help your heart work
better as a pump. You may also have medicines available
to help reduce anxiety or pain, and something to help
you sleep. Please let your nurses know how you are feeling.
The day before you are discharged, your doctor will
be making decisions about your medicines for home. The
pharmacist will be available to talk with you about
what you will be taking at home. Be sure you understand
what you will be taking at home. If you would like more
information about your medicine, tell your nurse.
Guide to LEARNING in the Hospital
Please help us by sharing what you know about congestive
heart failure and how you manage at home. We will need
to know whether you have a home scale and are able to
use it, or if you would be able to get one. You will
receive a packet of information to use here and to take
home with you. You will learn about this condition and
how you can manage it when you leave the hospital.
We will review with you what congestive heart failure
is, what causes the symptoms you have had, and what
other symptoms you might experience. To help you with
this, we have four short videos about Congestive Heart
Failure for you to watch while you are in the hospital.
Every day you are here you will be offered the chance
to watch the videos on congestive heart failure. Please
ask questions if you don't understand something.
While you are here you will learn about your medicines
and healthy food choices for a 2 gram sodium diet. It
will be important to weigh yourself every day after
you leave the hospital. You will learn about the record
sheets we have for you to use to record your weights.
Please take your weight records to your doctor appointments.
It will be important for you to learn what symptoms
and signs you should report to your doctor and when
to call for questions.
On the day you leave the hospital, we want to be sure
you understand the discharge instructions from you doctor
and your plan of care for home, including when to call
your doctor and when your next appointment is scheduled.
Your nurse, doctor, and/or a pharmacist will review
your medicines for home. If you have any questions,
do not hesitate to ask. Share any concerns you may have
so that we can make the move from the hospital to home
easy and less stressful.
After you have gone home, a nurse may call you to check
on how you are managing and answer any questions you
may have.
We hope your stay has gone smoothly, that you received
the care you needed, and that you have everything for
your return home.
Best wishes for a speedy recovery!
Booklet compliments of the CHF Care Map Team
Patient & Family Education Council 9/2000
DAILY WEIGHT
Follow these instructions:
Weigh yourself at the same time each day. In the morning
before breakfast is the best time.
Wear the same amount of clothing each time.
Empty your bladder before weighing.
Use the same scale each time.
Adjust the scale to the "zero point" each time.
If you use a spring type scale, put it on a hard surface,
as carpeting may cause it to give wrong number.
Keep a written record of your weights on the back of
this sheet and bring it with you to each doctor visit.
Call your doctor if your weight increases 2-3 pounds
over a week
Weight / Symptom
Record Month:__________
Take with you to all doctor appointments
Weigh each day: Check boxes that apply to you each
day:
|
Date
|
Weight
|
Fatigue
|
Short
of breath/cough
|
Foot
or ankle swelling
|
Using
more pillows to sleep |
No
problems |
| 1 |
|
|
|
|
|
|
| 2
|
|
|
|
|
|
|
| 3
|
|
|
|
|
|
|
| 4
|
|
|
|
|
|
|
| 5
|
|
|
|
|
|
|
| 6
|
|
|
|
|
|
|
| 7
|
|
|
|
|
|
|
| 8
|
|
|
|
|
|
|
| 9
|
|
|
|
|
|
|
| 10
|
|
|
|
|
|
|
|