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What is anemia?
Blood level is low
Deficiency in the number of erythrocytes, the quality or quality of hemoglobin, and/or volume of packed RBCs (hematocrit)
What happens during anemia?
Decrease of hemoglobin and hematocrit
What are major signs of anemia?
Fatigue — Don’t have enough RBCs
Discoloration — Jaundice (Bilirubin)
What are types of anemia?
Iron Deficiency Anemia — dietary, malabsorption, blood loss, or hemolysis
Thalassemia minor/major — inadequate production of normal hemoglobin
Megaloblastic or Pernicious Anemia — Cobalamin or B-12 deficiency due to impaired DNA synthesis or absorption issues
Anemia or Chronic Disease — associated with underproduction of RBCs (serious chronic illness or medications that suppress immune system) or chronic blood loss (gastritis/bleeding ulcers, hemorrhoids, menstruation, etc.)
Chronic or acute blood loss
Increased RBC Destruction — Hemolysis: ex. Sickle cell, medications, trauma, etc.
Iron Deficiency Anemia
Dietary, malabsorption, blood loss, or hemolysis (destruction of RBCs)
Thalassemia minor/major
Inadequate production of normal hemoglobin
Blood transfusion — Disadvantage
Megaloblastic or Pernicious Anemia
Cobalamin or B-12 deficiency due to impaired DNA synthesis or absorption issues
Anemia of Chronic Disease
Associated with underproduction of RBC’s — serious chronic illness or medications that suppress the immune system
OR
Chronic blood loss (gastritis/bleeding ulcers, hemorrhoids, menstruation, etc.)
Nursing assessment for Integumentary Manifestations
Pallor
Jaundice
Pruritus
Why does pallor (pale skin) occur with anemia?
Decrease of hemoglobin and blood flow to the skin
Why does jaundice (yellowing skin) occur with anemia?
Increase concentration of serum bilirubin
Why does pruritus (itchy skin) occur with anemia?
Increase serum and skin bile salt concentrations
What are the cardiopulmonary manifestations of anemia?
Cardiac output maintained by increasing heart rate and stroke volume due to inadequate O2 in tissues
Clinical Manifestations of Integumentary
Pallor, cyanosis, jaundice
Clinical Manifestations of mucous membranes
Pallor
Clinical Manifestations of Tongue
Shiny, beefy red, smooth, glossitis (inflammation of tongue)
Clinical Manifestations of Eyes
Conjunctival pallor (pale color of inner lining of the lower eyelid), scleral icterus (yellowing of eyes), retinal hemorrhage (bleeding in eyes)
Clinical Manifestations of Cardiopulmonary
Tachycardia, palpitations, angina (chest pain/discomfort), systolic murmur, MI, intermittent claudication (muscle pain, cramping, or weakness in the legs)
Clinical Manifestations of Respiratory
Dyspnea on activity, low SpO2
Clinical Manifestations of Abdomen/GI
Splenomegaly (enlarged spleen), hepatomegaly (enlarged liver), sore mouth/difficulty swallowing
Clinical Manifestations of Neurological
Numbness, ataxia (poor muscle control that causes clumsy movements)
Clinical Manifestations of musculoskeletal
Bone pain
Clinical Manifestations of Constitutional
Weakness, fatigue, sensitivity to cold
Major diagnosis of anemia
Fatigue
Imbalanced nutrition
Ineffective health management
What are the nursing interventions for anemia?
Alternate rest and activity
Prioritize activities: accommodate energy levels, maximize O2 supply
Provide assistance to minimize risk for injury
Evaluate nutritional needs
What are the risk factors for iron deficiency anemia?
Older adults
Poor diet
Menstruating and pregnant women
What are the management priorities for iron deficiency anemia?
Iron rich diet
Iron supplementation (Consider taking with acidic foods)
Discusses patient education for Iron Replacement Therapy
What safety measures needs to be taken with iron deficiency anemia?
Liquid iron should be diluted and ingested through a straw — can stain teeth
Bleeding/bruising precautions
What are the patient and family teachings that need to be done?
Diet teaching — foods high in iron and how to maximize absorption
Discuss the need for diagnostic studies to identify the cause
Emphasize compliance with dietary and drug therapy
Patients who require lifelong iron supplementation should be monitored for potential liver problems related to iron storage
What is iron best absorbed as in what environment?
Ferrous sulfate in an acidic environment
When should iron be taken?
An hour before means when duodenal is most acidic
Avoid binding iron with food
What food/vitamin can be taken with iron?
Vitamin C (ascorbic acid) and orange juice enhance iron absorption
Why should people ingest iron through a straw?
Undiluted iron may stain teeth
What can be a substitute for ferrous sulfate?
Ferrous gluconate
How does iron effect stool?
It turns the stool black because of excess iron
What does iron cause? What do they need to be started on?
Causes constipation, so patients should be started on stool softeners and laxatives if needed
What is the primary cause of pernicious anemia?
Absence of intrinsic fluid
This protein is required for the body to absorption B-12 in the intestines
What are other causes of pernicious anemia?
GI surgery
Chronic diseases of GI tract
Excessive alcohol
Smoking
Long-term users of H2-histamine receptor blockers and proton pump inhibitors
Strict vegetarians
What is most commonly caused by pernicious anemia?
Cobalamin deficiency
Which results in poor cobalamin absorption through the GI tract
What are megaloblastic anemias?
A group of disorders caused by impaired DNA synthesis and characterized by the presence of large RBCs
Most common cause of megaloblastic anemia
Cobalamin (vitamin B-12) and/or folic acid deficiencies
Less common causes of megaloblastic anemia
Suppression of DNA synthesis by drugs
Inborn errors of cobalamin and folic acid metabolism
Erythroleukemia — Malignant blood disorder: A proliferation of erythropoietic cells in bone marrow
What is anemia of chronic illness associated with?
Cytokine (interleukin 6) release causing retention of iron in macrophages
Chronic inflammatory process, autoimmune disorder, infectious disorder, (HIV, malaria, hepatitis), malignancy, heart failure
How is anemia of chronic illness different from anemia of other causes?
Reaction aimed at underlying condition
May require blood transfusion
Erythropoietin cautiously
Teach activity modifications
Dietary considerations
What are the causes of acute blood loss?
Trauma
Surgical and surgical complications
What are the concerns related to acute blood loss?
Volume loss and hypovolemic shock
Less sudden loss may compensate with correcting volume loss, but HCT fall is significant
Bleeding ulcer with loss of 750 mL hematemesis over 30 minutes
May have postural hypotension, but normal HGB and HCT, but over next 1-2 days H and H will fall because of intravascular fluid increases (Extravascular to intravascular) and ADH and aldosterone
What are the assessments for anemia from acute blood loss?
Dependent on location of bleeding
Pain from tissue distension, organ displacement and/or nerve compression
Pallor, dusky, cold, clammy skin
Tachycardia, Tachypnea and Hypotension, especially postural
Evidence of slower bleeding
What symptoms are evidence of slower bleeding?
Stools
Urine
Retroperitoneal
Change in heart sounds (muffled)
Diminished lung sounds
Ecchymosis
Abdominal distention
Reduced peripheral pulse strength
Peripheral pallor
What is the adult vascular volume?
Around 5L
Medical management for acute blood loss
Laboratory
Blood bank
Surgical consult
Nursing interventions for acute blood loss
ABC’s
Identify cause — assessment matters
Oxygenation considerations
Volume replacement — need venous access
Common blood products used for replacement
Long term — iron replacement
What are common blood products used for replacement for acute blood loss?
Crystalloid (normal saline, lactated ringers solution)
Packed red blood cells
Plasma for clotting replacement
Platelets
Consider calcium needs
What are the two types of hemolysis?
Intrinsic hemolysis
Extrinsic hemolysis
How does intrinsic hemolysis come from?
Most often hereditary
What is the prototype for anemia from hemolysis?
Sickle cell disease
What needs to be focused on for intrinsic hemolysis?
Preventing dehydration, increased tissue oxygen needs, and infection
Where does extrinsic hemolysis come from?
From physical destruction, antibody reactions, infectious agents and toxin
What is the most important site for RBC destruction?
Spleen
What is polycythemia?
A myeloproliferative disorder that results in the overproduction and presence of increased numbers of RBC’s
What can result from polycythemia?
This can result in impairment in blood circulation due to the viscosity of the blood as well as hypervolemia
What are the symptoms of polycythemia?
Viscous blood due to high RBC count
Vertigo, headache, tinnitus, visual disturbances
Generalized pruritus — exacerbated by hot bath — due to histamine release from increase number of basophils
Angina, heart failure, intermittent claudication, thrombophlebitis
What are the nursing interventions for polycythemia?
Phlebotomy — for acute exacerbations
Monitor I & O to prevent overload and dehydration
Myelosuppressive agents (suppress bone marrow function) — give as directed and teach patient about potential side effects
Assess nutritional status and provide appropriate teaching
Activities and medications to decrease thrombus formation
Supportive care
What is aplastic anemia?
A condition that occurs when the body stops producing enough new blood cells
How does aplastic anemia affect the body?
It leaves the body fatigued and more prone to infections and uncontrolled bleeding
What are the clinical manifestations for aplastic anemia?
Fatigue
Shortness of breath
Rapid or irregular heart rate
Pale skin
Frequent or prolonged infections
Unexplained or easy bruising
Nosebleeds and bleeding gums
Prolonged bleeding from cuts
Skin rash
Dizziness
Headache
What is the most common cause of aplastic anemia?
The immune system attacking stem cells in the bone marrow
What are other factors that can injure the bone marrow and affect blood cell production?
Radiation and chemotherapy treatments
Exposure to toxic chemicals
Use of certain prescription drugs — such as chloramphenicol
Autoimmune disorders, certain blood diseases, and serious infection
A viral infection
Pregnancy
What are prevention tactics for aplastic anemia?
There’s no prevention for most cases of aplastic anemia
Avoiding exposure to insecticides
Herbicides
Organic solvents
Paint removers
Other toxic chemicals might lower the risk of the disease
What is normal hemostasis?
Involves the vascular endothelium, platelets, and coagulation factors
They function together to stop hemorrhage and repair vascular injury
Disruption of any component may result in bleeding or thrombotic
What is thrombocytopenia?
A reduction of platelets
Result of thrombocytopenia
Abnormal hemostasis
Prolonged or spontaneous bleeding
What is thrombocytopenia commonly from?
Ingestion of high doses of certain drugs (chemotherapy, etc)
What is the range of thrombocytopenia?
Below 150,000/microliters
What are acquired problems that arise from a reduction in platelet count?
Immune Thrombocytopenic Purpura (ITP)
Thrombotic Thrombocytopenic Purpura (TTP)
Heparin Induced Thrombocytopenia (HIT)
What are laboratory findings for thrombocytopenia?
Low platelet count <150 K
Prolonged bleeding from trauma or injury at platelet counts < 50 K
Spontaneous, life-threatening hemorrhage at platelet counts < 20 K
Assessment for Thrombocytopenia
Epistaxis, gingival bleeding, petechiae, purpura, superficial ecchymoses
Prolonged bleeding after routine procedures
Weakness, tachycardia, dizziness, abdominal pain, hypotension
Hemorrhage insidious, acute or severe — joints, retina, cerebral
Nursing assessment for thrombocytopenia
Vital signs — Check for fever, tachycardia, and hypotension
Question carefully about any overt or covert
Do a complete medication assessment including OTC medications
Question more thoroughly these symptoms:
Pain
Stool cool
Bleeding gums
Changes in menses
Vomiting blood
Easy bruising
Headaches
Bloody urination
Nursing interventions for thrombocytopenia
Prompt follow-up evidence of bleeding tendency — prolonged nose bleed, petechiae; “Minor” bleeding may be only visible sign of internal bleeding
Monitor medications that may affect platelet counts — discourage use of OTC meds especially aspirin and aspirin containing medications
Monitor blood counts and coagulation studies — D-dimer, PT, aPTT
Monitor menstrual bleeding
Prevent injury:
Avoid injections, use smallest gauge possible, apply direct pressure after injections and venipunctures for 5-10 minutes
Use of ice packs
Assess ability to self-ambulate — keep “traffic pattern” clear, call light available
Soft bristle toothbrush
Avoid intramuscular injections
What is considered Heparin Induced Thrombocytopenia?
An immune-mediated response resulting in premature platelet destruction and platelet-fibrin thrombus formation
Manifestations of Heparin Induced Thrombocytopenia
Dyspnea
Bruising
Hypertension
Anxiety
Interprofessional Care for Heparin Induced Thrombocytopenia
Permanently stop all heparin including heparin flushes
Start the patient on a direct thrombin inhibitor
Start warfarin (Coumadin) when platelet count reaches 150,000/microliter
For severe clotting:
Plasmapheresis to clear platelet-aggregating IgG from the blood
Protamine sulfate to interrupt circulating heparin
Thrombolytic agents to treat thromboembolic events
Surgery to remove clots
When must heparin be discontinued?
When HIT is first recognized
How should you maintain anticoagulation when heparin is discontinued?
The patient should be started on a direct thrombin inhibitor, such as lepirudin (Refludan) or argatroban (Acova)
When should Coumadin be started?
When the platelet count has reached 150,000/microliter
People who have heparin induced thrombocytopenia should never be given what?
Heparin or low-molecular-weight heparin
What are the risk factors of thromboembolism (Deep vein thrombosis - DVT)?
Venous stasis
Endothelial damage
Hypercoagulability of blood
What are the nursing processes for DVT?
Assessment
Analysis
Planning
Implementation
Evaluation
Management Priorities
Safety
Patient and family teaching
Psycho-social/Spiritual Considerations
What are ways to prevent Deep Vein Thrombosis?
Graduated Compression Stockings
Early and Aggressive Mobilization
SQ Heparin/Lovenox
What are the diagnostics and labs that you should look out for with Deep Vein Thrombosis?
Hematocrit and Hemoglobin
Platelet count
D-dimer
Coagulation Studies: INR, aPTT, Activated Clotting Time (ACT), Anti-factor Xa
*Link each of these labs with medications. Which lab would you follow based on what med the patient was prescribed?
Medical treatment for DVT
Medication Therapy:
Heparin gtt with a bridge to Coumadin
Other long-term anti-coagulants
Catheter-guided admin of thrombolytic drugs (tPA)
Surgical intervention for DVT
Venous Thrombectomy
IVC Filter Placement
Nursing management for Acute DVT
Prevention is first! But if that doesn’t:
Manage pain
Follow labs
Administer medications
Nursing management for Chronic DVT
Dietary and medication teaching
Lifestyle teaching — smoking, weight management, oral contraception, mobility
Nursing care for Heparin protocol
Monitor labs and make prompt changes as described in order set
Monitor for complications of thromboembolism — Shortness of breath, angina, and change of mental status are most significant/life threatening
Prevention is key! — Venous Thromboembolism (VTE) is a major hospital associated risk
What is Neutropenia?
When a person has a low level of neutrophils
Where are neutrophils made?
Bone marrow
What are the signs and symptoms of neutropenia?
A fever
Chills or sweating
Sore throat, sores in the mouth, or a toothache
Abdominal pain
Pain near the anus
Pain or burning when urinating, or urinating often
Diarrhea or sores around the anus
A cough or shortness of breath
Any redness, swelling, or pain — especially around a cut, wound, or catheter
Unusual vaginal discharge or itching
What are the causes of neutropenia?
Some types of chemotherapy
Cancers that will affect bone marrow directly — Leukemia, lymphoma, and multiple myeloma
Cancers that spread
Radiation therapy — To body or to bones in the pelvis, legs, chest, or abdomen
Vitamin deficiencies, most commonly vitamin B12, folate, and copper deficiency
Sepsis — an infection of the bloodstream
Pearson syndrome
Certain infections — Including Hepatitis A, B, and C, HIV/AIDS, malaria, tuberculosis, dengue fever, and Lyme disease
Hypersplenism or enlarged spleen
Neutropenia Lab Values
Between 2.0 and 7.5 × 10^9/litre — Not neutropenic
Less than 2.0 and 10^9/litre — Neutropenic
Less than 0.5 × 10^9/litre — Severely neutropenic
Nursing interventions for Neutropenia
Educate patient on infection prevention strategies, including meticulous hand hygiene, avoiding crows, and maintaining a clean living environment
Emphasize the importance of promptly reporting any signs of infection
The nurse should place the patient in a private room and institute neutropenic precautions (REVERSE ISOLATION)
Administer medications as ordered