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What does bone marrow produce
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ESR- erythrocyte sedimentation rate
test the measures the settling of the rbcs in a test tube
When it is settling it means that that pt may have an acute infection
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Complete Blood Count consists of
Hemoglobin and Hematocrit
-
Normal # for RBCs
4,200,000 to 6,100,000/mm3
-
Normal # for WBCs
(5,000-10,000/mm3)
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Normal # for Platelets
150,000-400,000/mm3
-
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PT
Prothrombin Time 11-12.5 sec
test to evaluate hemostasis
-
PTT
Partial Thromboplatin Time 30-45 sec
The PTT evaluates thecoagulation factors
-
INR
International normalized ratio
normal range 0.7-1.8
- when on warfarin – range 2-3
- desired levels may vary according to patient condition
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Bleeding Time
1- 9 mins
They slit your arm and put gauze on it, then time how long it takes for you to stop bleeding
Drugs like aspirin and Motrin will effect the bleeding time
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Radiologic Studies (diagnostic studies hemolytic system)
CT and MRI
-
Biopsies used in
– Bone marrow, Lymph Node
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What would be primary nursing concerns for a patient post-procedure bone marrow biopsy?
-
What Position is the pt in for a Bone Marrow biopsy
prone or side lying
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What should you educate the pt with when the are getting a bone marrow biopsy
Educate them on what to expect and feel
Some patients say they can feel the pressure of the needle going into their hip
Tell them they are conscious for sedation (local anesthetic)
-
What kind of technique is used for Bone marrow biopsy
Sterile
because you are going right into the bone
-
What kind of Post Care do you want to do for your pt after a Bone Marrow biopsy
•Prevent bleeding (may have to put pressure on site)
•Check for infection
•Pain relief
•Ice packs- vasoconstrict, stop bleeding
•Avoid contact sports
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Anemia
- Deficieny of RBCs
- Low Hgb and Hct
•Not a specific disease but rather a manifestation of a pathologic process
-
Main Manifestation of Anemia
tissue Hypoxia
-
Integumentary Manifestations of Anemia
- Pallor, especially of the ears, the nail beds, the palmar creases, the conjunctivae, and around the mouth
- •Cool to the touch
- •Intolerance of cold temperatures
- •Nails become brittle and may lose the normal convex shape; over time, nails become concave and fingers assume clublike appearance
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Cardio Manifestations of Anemia
Tachycardia at basal activity levels, increasing with activity and during and immediately after meals
•Murmurs and gallops heard on auscultation when anemia is severe
•Orthostatic hypotension
-
Respiratory Manifestations of Anemia
- Dyspnea on exertion
- Decreased oxygen saturation levels
-
Neurologic Manifestations of Anemia
- Increased somnolence and fatigue
- Headache
-
What are the 3 Anemias Caused by Decreased Erythrocyte Production
•Decreased Hb synthesis (Fe+ deficiency)
•Defective DNA synthesis (Folic acid deficiency)
•Decreased availability of erythrocyte precursors (Aplastic anemia)
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Iron-Defficiency Anemia is from
•inadequate diet malabsorption, blood loss, hemolysis
-
Clinical Manifestations of Iron-Defficiency Anemia
•headache, inflammation of tongue and cheilitis (inflammation of lips),
-
Cheilitis
Inflammation of lips
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Diagnostic studies found in Iron-Defficiency Anemia
- increase TIBC,
- low serum iron,
- H/H low
-
How do you know its iron deficiency
Take a blood test
We need iron for the hgb to attach to the rbc
ron will be low
Hgb/Hct low
Classic for iron deficiency- TIBC (total iron binding capacity) will increase
-
TIBC is performed to rule out
Iron-Deficiency Anemia
IF you have iron deficiency this test will be increased
If the rbcs are not holding onto the iron- then they have a greater capacity to hold onto iron
-
Drug Therapy for Iron-Deficiency Anemia
•GI side effects esp. constipation
- •Take between meals to reduce GI distress and
- improve absorption
•Liquid take with straw
side effects: black stool, constipation
-
Assess pt with Iron-Deficiency Anemia for
Hypoxemia
-
Nursing Management: Iron-Deficiency Anemia
•Administer O2 as ordered
•Alternate rest/activity
•Monitor VS, hgb/hct
•Teach about meds
•Transfuse with blood products if needed- pRBC’s
-
Teach pt with Iron Deficiency Anemia about a Diet
•Increase protein and iron (b/c hemoglobin is made of protein)
•Small, frequent meals
•Increase iron-rich foods (red meat, kidney beans, green leafy vegetables etc)
-
Megaloblastic Anemias
Cobalamin Deficiency
Folic Acid Deficiency
-
Cobalamin Deficiency is
Vit B12 deficiency
Lack of Intrinsic Factor (IF)
-
Clinical Manifestations of Cobalamin Deficiency
sore tongue, N/V, weakness, paresthesia of feet and hands, ataxia, confusion, pallor
-
Diagnostic studies for Cobalamin Deficiency
- macrocytic RBC’s,
- decreased cobalamin,
- Schilling test for IF absorption
-
Nuero Signs are classic in what Anemia
Cobalamin
Confusion and Ataxia
-
Ataxia
Lack of muscle coordination
-
Why is the intrinsic factor important
it allows the absorption of Vit. B12
if you are lacking IF than you are not able to absorb B12 causing Cobalamin anemia
-
What does Shillings test test for
used to determine whether the body absorbs vitamin B12 normally
-
Collabrative care for a pt with Cobalamin Anemia
•supplemental Vit. B12 IM for pernicious anemia,
•Increase dietary B12 (not for pernicious anemia)
•CaloMist – B12 nasal spray – maintain vitamin levels
-
Pernicious Anemia is the Lack of
Intrinsic Factor which causes Vit. B12 Not to be aborbed
supplemental Vit. B12 has to be given IM
-
Cobalamin Anemia is the lack of
B12 but the Intrinsic Factor is still working properly
Supplemental Vit B12 can be given by Diet
-
Folic Acid Deficiency Anemia causes
poor nutrition, malabsorption, drugs, alcohol abuse,
-
What is Folic Acid needed for
needed for DNA synthesis leading to RBC formation
-
Folic Acid Deficiency Anemia Clincal Manifestations
sore tongue, N/V, weakness, paresthesia of feet and hands, pallor
No changes in Neuro signs
-
Folic Acid Deficiency Anemia Treatment
Folic acid replacement (1mg), diet high in folic acid
-
Aplastic Anemia
deficiency of RBC
•Congenital due to chromosomal alterations
•Acquired due to exposure to chemicals, radiation, medications, bacteria, viruses
-
Pancytopenia
deficiency of RBC, WBC and platelets
-
What would the nurse expect to assess in the patient with Aplastic Anemia
Signs of infection- increased WBC, fever, depressed
First clue may be a sore throat
-
Diagnostic studies for pts with Aplastic Anemia
RBC, WBC and platelet counts, TIBC, bone marrow study
-
Nursing and Collaborative Management for a pt with Aplastic Anemia
•Bone marrow transplant
•Immunosuppression with cyclosporin, etc.
•Prevent complications from infection and hemorrhage
-
Because Immunosuppresion is a treatment for Aplastic Anemia how can we prevent further infections
Wear Gloves and Wash Hands
-
What assessment do you want to narrow in on for Aplastic Anemia
NEURO assessment
Can be a sign of hypoxia
For bleeding or infection
Bleeding may occur first in the brain- confusion, change in mental status, stroke like symptoms, septic
-
What is a Caution for visitors visiting Aplastic Anemia
Screen visitors
Anyone with a cold or infection should not be in there
Children may not be sick but may be carrying an infection- so some kids may not be aloud in
Avoid invasive Procedures
-
What kind of room do you want for a pt with Aplastic Anemia
Private room and possible isolation
private room if their WBC is really low
-
Acute Anemia caused by blood loss
sudden blood loss due to trauma or surgery
-
Chronic Anemia caused by blood loss
- gradual blood loss where body adapts but there is insufficient RBC’s – GI bleeding, excessive
- menstruation
-
Collaborative care for Acute Anemia blood loss
•replacing volume, prevent shock, blood transfusions, iron supplements etc
-
What are the steps to stop Acute Anemia blood loss
- replace blood volume,
- ID source of hemorrhage and stop bleeding,
- administer dextran,
- Hetastarch, a
- lbumin,
- lactated
- Ringer’s,
- supplemental iron.
-
Nurse Management for Acute blood loss
•Post OP – monitor incision sites, drainage tubes, and dressings for blood loss.
•Administer O2 therapy – monitor O2 saturation
•Administer fluids, electrolytes, blood transfusions
•Administer meds to increase production of RBC’s
-
Nurse Management for Chronic Blood loss
•ID source of bleeding and stop bleeding
•Nursing management is same as for iron-deficiency anemia
-
Polycythemia
•Increased production of RBC’s causing impaired circulation due to increased blood viscosity
-
What is the Nursing Priority for Polycythemia
Hydration for fluid balance because blood is very viscous
-
Primary - Polycythemia vera
– form of cancer in which there is an increase in RBC, WBC and platelets (cells are often impaired)
-
Secondary (Polycythemia)
•hypoxia stimulates erythropoietin in kidneys which increase production of RBCs
•Hepatomegaly, spleenomegaly, intermittent claudication, pain,
-
Diagnostic studies for Polycythemia
•Hb, rbc, wbc, platelets, (frequent)
• bone marrow examination
at some time the dr. takes blood out of body and puts some back in
-
Collabrative care for Polycythemia
- Hydration
- frequent small meals
- Avoid iron supplements
- Avoid Citrus with meals
-
Why wont Aspirin work for Polycythemia
Because this is a clumping problem not a clotting problem that has to do with platelets
So aspiriin will not help
-
Why do we want to avoid Citrus foods with meals with Polycythemia
citrus increases absorption of iron
-
What can we look for on the pt with Polycythemia ??
Bruises on places that are not normal for day to day activities and play
-
myelosuppressant agents
Reduce bone marrow activity
used in pts with Polycythemia
-
What are pts at risk for if they have Polycythemia
Hyperkalemia: becuase Once the cells die they are going to release potassium
Stroke: because blood is viscous and moves slower
-
Thrombocytopenia
Low platelet count
Which means patient has problems with clotting
-
•Immune Thrombocytopenic Purpura –
(idiopathic thrombocytopenic Purpura)
autoimmune disease that causes abnormal platelet destruction
-
Thrombotic Thrombocytopenic Purpura
–formation of micro-thrombi/platelets that deposit in arterioles and capillaries resulting in few platelets in circulation
-
Thrombocytopnia Clinical Manifestations
•Petechiae, ecchymoses, prolonged bleeding after routine procedures, major complication is hemorrhage
-
Diagnostic Studies for Thrombocytopenia
•Platelet count (decreased), bleeding time (prolonged), bone marrow, Hb/Hct
-
•Collaborative Care
Immune Thrombocytopenic Purpura
corticosteroids, IV immunoglobulin,, splenectomy, platelet transfusion
-
Collaborative Care
Thrombotic Thrombocytopenic Purpura
•corticosteroids, plasma exchange, anti-platelet agents
-
Leukopenia
–is a reduction in the total number of WBC
-
Neutropenia
reduction in number of neutrophils (granulocytopenia)
•Syndrome that occurs with a variety of illness
•Classic signs of infection or inflammation may not occur
-
Neutropenia Diagnostic studies
- Low Neutrophil Count 1000-1500, peripheral
- blood smear to assess for immature cells, bone marrow aspirations
may not have typical signs of infection
Patients may not have the fever
So you have to look outside the box to figure it out
-
Collabrative Care for Neutropenia
•Alert for minor complaints (sore throat, diarrhea, low grade fever etc)
•Antibiotics
•Screened visitors
•Strict handwashing- MUST
- •Private room (Laminar air flow rooms if needed)- protective isolation (you are protecting the
- patient, not yourself)
•Avoidance of fresh fruits and vegetables (severely compromised)- because of the bacteria on the outside of them
-
Leukemia
•A group of malignant disorders affecting the blood and blood-forming tissues of
•Bone marrow
•Lymph system
•Spleen
•Accumulation of dysfunctional cells due to loss of regulation in cell division
-
Patient can have Leukemia in responce to what
Chemotherapy
-
Hemostasis
the process that the body uses to form blood clots to help stop bleeding.
-
Prolonged PT but normal PTT
liver disease
-
the PTT and PT tests are sometimes selectively performed as pre
Pre-surgical procedures to screen for potential bleeding tendencies.
-
Acute Leukemia
symptom occur rapidly and without intervention will progress to death
-
Leukemia Cells cause
•Splenomegaly
•Hepatomegaly
•Lymphadenopathy
- •Bone pain- immature
- cells
-
Leukemia Cells invade
•Meningeal irritation
•Oral lesions
•Solid masses
-
Hodgkins Disease
a malignant condition caused by proliferation of abnormal, giant, multinucleated cells called Reed-Steinberg cells located in the lymph nodes
- enlarged cervical, axillary or inguinal nodes, fever,
- fatigue, night sweats
-
Non- Hodgkins Disease
malignant neoplasms of the immune system (lymphoid cancers that do not include Reed-Steinburg Cells)
painless lymph node enlargement
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