Chapter 24 Nursing Care of Patients with Hematopoietic
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Transcript Chapter 24 Nursing Care of Patients with Hematopoietic
Nursing Care of Patients with Hematologic
and Lymphatic Disorders
Deficiency of Red Blood Cells, Hemoglobin, or
Both
◦ Impaired Production
◦ Increased Destruction
◦ Blood Loss
Reduced Capacity to Carry Oxygen to Tissues
Dietary Deficiencies
Hemolysis
Hereditary Disorders
Pallor
Tachycardia
Tachypnea
Irritability
Fatigue
Dyspnea
Pernicious Anemia
◦ Numb Hands or Feet
◦ Sore Tongue
Iron Deficiency
◦ Mouth Fissures
◦ Glossitis
◦ Spoon-shaped Nails
CBC with Microscopic Examination
Bone Marrow Analysis
Tests to Determine Source of Bleeding
Eliminate Cause
Dietary Changes
Supplements
Transfusions
Activity Intolerance
Imbalanced Nutrition
Risk for Injury
Impaired Oral Mucous Membranes
Bone Marrow Does not Produce Adequate
RBCs
Causes
◦ Congenital
◦ Exposure to Toxins
◦ Chemotherapy
Weakness
Fatigue
Pallor
Dyspnea
Headache
Ecchymoses
Petechiae
Frank Bleeding
Infection
Death
Diagnosis
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CBC
Bone Marrow Biopsy
TIBC
Serum Iron
Treatment
◦ Treat Cause
◦ Colony Stimulating
Factors
◦ Steroids
◦ Bone Marrow
Transplant
Inherited
Autosomal
Recessive Disorder
Diagnosis
◦ Sickledex Test
◦ Hemoglobin
Electrophoresis
◦ CBC
◦ ESR
Crisis Treatment
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Antibiotics
Pain Management
Transfusions
Fluids
Oxygen
Avoid Risk of Reduced Oxygenation
◦ Exposure to Cold
◦ Infection
◦ Strenuous Exercise
Low Dose Penicillin
Frequent Transfusions
Hydroxyurea
Risk for Ineffective Tissue Perfusion
Acute Pain
Avoid
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Tight Clothing
Strenuous Exercise
Alcoholic Beverages
Cold Temperatures
Smoking
Unpressurized Aircraft
Exposure to Infection
Overabundance of Red Cells
Hemoglobin >18 mg/dL
Hematocrit >55%
Blood Becomes Thick
◦ Primary
◦ Secondary
Hypertension
Visual Changes
Headache
Vertigo
Dizziness
Tinnitus
Bleeding
Chest Pain
Dyspnea
Dark, Flushed Skin
Itching
Phlebotomy
Low Dose Aspirin
Chemotherapy
Radiation Therapy
Drink 3 Liters of Water Daily
Avoid Restrictive Clothing
Elevate Feet
Report Signs and Symptoms of Iron
Deficiency
Report Signs and Symptoms of Bleeding
Pathophysiology
◦ Accelerated Clotting
◦ Clotting Factors Depleted
◦ Bleeding
Etiology
◦ Major Trauma
Abnormal Bleeding
Joint Pain
Nausea and Vomiting
Organ System Failure
Convulsions
Shock, Coma
Death
Easy Bruising
Petechiae
Blood in Urine
Black Tarry Stools
Bleeding from Nose or Gums
New Onset of Painful Joints
PT, PTT
Platelet Count
Hbg
Hemoglobin, Creatinine
Correct Underlying Cause
Administer
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Blood
FFP
Platelets
Cryoprecipitates
Recognize and Report Bleeding
Avoid Trauma and Further Bleeding
Teach Patient and Family
Pathophysiology
◦ Platelet Destruction by Immune System
◦ Risk for Bleeding
Etiology
◦ Acute Viral Illness
◦ Drug Reaction
◦ Immune System Dysfunction
Bleeding
◦ Petechiae
◦ Ecchymoses
◦ Bleeding
Platelet Count
Bleeding Time
Bone Marrow Aspiration
Steroids
Chemotherapy
Transfusions
Vitamin K
Chemotherapy
Splenectomy
Bleeding Precautions
Recognize and Report Signs and Symptoms
Bleeding
Teach Patient and Family
Use Electric Razor
Use Soft Toothbrush
Avoid Invasive Procedures, Injections
Maintain Pressure if Blood Draw Essential
Wear Shoes or Slippers
Avoid Bumps and Bruises
Avoid Aspirin and Nsaids
Administer Stool Softener
Handle Patient Gently
Gentle Nose Blowing
Pathophysiology
◦ Missing Clotting Factors
A—Factor VIII
B—Factor IX
Etiology
◦ Heredity
Bleeding
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Joints
Muscles
Subcutaneous Tissue
Brain
PTT
Factor Levels
Desmopressin
Clotting Factors
◦ Factor VIII
◦ Factor IX
Blood Transfusion
Pain
Ineffective Protection
Risk for Ineffective Self Health Management
Pathophysiology
◦ Increase in Immature WBCs
◦ Unable to Fight Infection
Risk Factors
◦ Viruses
◦ Genetic Factors
◦ Radiation/Chemotherapy
Acute Lymphocytic Leukemia
Acute Myelogenous Leukemia
Chronic Lymphocytic Leukemia
Chronic Myelogenous Leukemia
Fever
Infection
Pallor
Weakness
Tachycardia
Palpitations
Dyspnea
Abdominal Pain
Malaise
Sternal/Rib Pain
CNS Changes
Bleeding
CBC
Bone Marrow Aspiration
Lumbar Puncture
Genetic Analysis
Chemotherapy
Radiation Therapy
Bone Marrow Transplant
Peripheral Blood Stem Cell Transplant
Risk for Injury: Infection, Bleeding
Fatigue
Impaired Oral Mucous Membranes
Knowledge Deficit
Anxiety
Pathophysiology
◦ Cancer of Plasma Cells in Bone Marrow
◦ Tumors Devour Bone Tissue
◦ Organ Invasion
Etiology
◦ Unknown
◦ Occupational Exposures
Bone Pain
Fever
Malaise
Spinal Cord Compression
Pathological Fractures
Hypercalcemia
Infection
CBC, Blood Calcium
Bone X-Rays
Urine for Bence
Jones Protein
Bone Marrow Biopsy
Steroids
Chemotherapy
Control of Serum Calcium
Radiation
Stem Cell Transplantation
IV Pamidronate (Aredia)
Risk for Infection
Risk for Injury
◦ Fracture
◦ Complications of Immobility
◦ Hypercalcemia
Cancer of Lymph System
◦ Presence of Reed-Sternberg Cells
Etiology
◦ Viral
◦ Genetic
◦ Immune Dysfunction
Painless Swollen Lymph Node
Pruritis
Pain Induced by Alcohol
Fever
Night Sweats
Weight Loss
Malaise
Edema of Face and Neck
Jaundice
Nerve Pain
Retroperitoneal Node Involvement
Spleen, Liver, and Bone Involvement
Biopsy
◦ Lymph Node
◦ Liver and Spleen
◦ Bone Marrow
CT, Chest X-Ray
Lung
Bone Scan
Lymphangiography
CBC
Stage I: Single Lymph Node or Site
Stage II: Two or More Nodes on Same Side of
Diaphragm
Stage III: Nodes on Both Sides of Diaphragm
Stage IV: Widely Disseminated Disease in
Organs or Tissues
Chemotherapy
Radiation Therapy
Impaired Comfort
Activity Intolerance
Risk for Infection
Risk for Ineffective Coping
Lymphoma Arising from B Cells and T Cells
Absence of Reed-Sternberg Cells
Etiology
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Some Viruses
H Pylori
Immune Dysfunction
Occupational Exposures
Painless Lymph Nodes
Enlarged Tonsils and Adenoids
Other Signs and Symptoms Similar to
Hodgkin’s Disease
Biopsy
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Lymph Nodes
Tonsils
Bone Marrow
Liver
Other
Bone Scan
CT, Chest X-ray,
IVP
MRI, PET Scan
Lymphangiography
CBC
Liver Function
Studies
Serum Calcium
Chemotherapy
Monoclonal Antibodies
Interferon Therapy
Radiation Therapy
Stem Cell Transplant
Activity Intolerance
Risk for Infection
Risk for Ineffective Coping
Hodgkin’s
◦ Less Common
◦ Age 15 to 40 and
>55
◦ Reed-Sternberg Cells
◦ Younger
◦ Good Prognosis
◦ Alcohol-induced Pain
Non-Hodgkin’s
◦ More Common
◦ Usually >Age 50
◦ Absence of ReedSternberg Cells
◦ Poorer Prognosis
Surgical Removal of the Spleen
Baseline Labs
Blood Transfusion if Necessary
Vitamin K
Baseline Vital Signs
Teach Coughing and Deep Breathing
Monitor for Bleeding
Monitor Vital Signs
Administer Narcotics for Pain
Encourage to Cough and Deep Breathe and
Ambulate
Bleeding
Pneumonia
Atelectasis
Infection
OPSI