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Chapter 28

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Chapter 28. Nursing Care of Patients with Hematologic and Lymphatic Disorders. Anemia. Deficiency of Red Blood Cells, Hemoglobin, or Both Impaired Production Increased Destruction Blood Loss Reduced Capacity to Carry Oxygen to Tissues. Etiologies. Dietary Deficiencies Hemolysis - PowerPoint PPT Presentation
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Nursing Care of Patients with Hematologic and Lymphatic Disorders
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Page 1: Chapter 28

Nursing Care of Patients with Hematologic and Lymphatic Disorders

Page 2: Chapter 28

Deficiency of Red Blood Cells, Hemoglobin, or Both◦ Impaired Production◦ Increased Destruction◦ Blood Loss

Reduced Capacity to Carry Oxygen to Tissues

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Dietary Deficiencies Hemolysis Hereditary Disorders

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Pallor Tachycardia Tachypnea Irritability Fatigue Dyspnea

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Pernicious Anemia◦ Numb Hands or Feet◦ Sore Tongue

Iron Deficiency◦ Mouth Fissures◦ Glossitis◦ Spoon-shaped Nails

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CBC with Microscopic Examination Bone Marrow Analysis Tests to Determine Source of Bleeding

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Eliminate Cause Dietary Changes Supplements Transfusions

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Activity Intolerance Imbalanced Nutrition Risk for Injury Impaired Oral Mucous Membranes

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Bone Marrow Does not Produce Adequate RBCs

Causes◦ Congenital◦ Exposure to Toxins◦ Chemotherapy

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Weakness Fatigue Pallor Dyspnea Headache

Ecchymoses Petechiae Frank Bleeding Infection Death

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Diagnosis◦CBC◦Bone Marrow Biopsy◦TIBC◦Serum Iron

Treatment◦Treat Cause◦Colony Stimulating

Factors◦Steroids◦Bone Marrow

Transplant

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Inherited Autosomal Recessive Disorder

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Diagnosis◦Sickledex Test◦Hemoglobin

Electrophoresis◦CBC◦ESR

Crisis Treatment◦Antibiotics◦Pain Management◦Transfusions◦Fluids◦Oxygen

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Avoid Risk of Reduced Oxygenation◦ Exposure to Cold◦ Infection◦ Strenuous Exercise

Low Dose Penicillin Frequent Transfusions Hydroxyurea

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Risk for Ineffective Tissue Perfusion Acute Pain

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Avoid ◦ Tight Clothing◦ Strenuous Exercise◦ Alcoholic Beverages◦ Cold Temperatures◦ Smoking◦ Unpressurized Aircraft◦ Exposure to Infection

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Overabundance of Red Cells Hemoglobin >18 mg/dL Hematocrit >55% Blood Becomes Thick

◦ Primary ◦ Secondary

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Hypertension Visual Changes Headache Vertigo Dizziness Tinnitus

Bleeding Chest Pain Dyspnea Dark, Flushed Skin Itching

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Phlebotomy Low Dose Aspirin Chemotherapy Radiation Therapy

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Drink 3 Liters of Water Daily Avoid Restrictive Clothing Elevate Feet Report Signs and Symptoms of Iron

Deficiency Report Signs and Symptoms of Bleeding

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Pathophysiology◦ Accelerated Clotting◦ Clotting Factors Depleted◦ Bleeding

Etiology◦ Major Trauma

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Abnormal Bleeding Joint Pain Nausea and Vomiting Organ System Failure Convulsions Shock, Coma Death

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Easy Bruising Petechiae Blood in Urine Black Tarry Stools Bleeding from Nose or Gums New Onset of Painful Joints

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PT, PTT Platelet Count Hbg Hemoglobin, Creatinine

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Correct Underlying Cause Administer

◦ Blood◦ FFP◦ Platelets◦ Cryoprecipitates

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Recognize and Report Bleeding Avoid Trauma and Further Bleeding Teach Patient and Family

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Pathophysiology◦ Platelet Destruction by Immune System◦ Risk for Bleeding

Etiology◦ Acute Viral Illness◦ Drug Reaction◦ Immune System Dysfunction

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Bleeding◦ Petechiae◦ Ecchymoses◦ Bleeding

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Platelet Count Bleeding Time Bone Marrow Aspiration

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Steroids Chemotherapy Transfusions Vitamin K Chemotherapy Splenectomy

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Bleeding Precautions Recognize and Report Signs and Symptoms

Bleeding Teach Patient and Family

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Use Electric Razor Use Soft Toothbrush Avoid Invasive Procedures, Injections Maintain Pressure if Blood Draw Essential Wear Shoes or Slippers

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Avoid Bumps and Bruises Avoid Aspirin and Nsaids Administer Stool Softener Handle Patient Gently Gentle Nose Blowing

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Pathophysiology◦ Missing Clotting Factors

A—Factor VIII B—Factor IX

Etiology◦ Heredity

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Bleeding◦ Joints◦ Muscles◦ Subcutaneous Tissue◦ Brain

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PTT Factor Levels

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Desmopressin Clotting Factors

◦ Factor VIII◦ Factor IX

Blood Transfusion

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Pain Ineffective Protection Risk for Ineffective Self Health Management

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Pathophysiology◦ Increase in Immature WBCs◦ Unable to Fight Infection

Risk Factors◦ Viruses◦ Genetic Factors◦ Radiation/Chemotherapy

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Acute Lymphocytic Leukemia Acute Myelogenous Leukemia Chronic Lymphocytic Leukemia Chronic Myelogenous Leukemia

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Fever Infection Pallor Weakness Tachycardia Palpitations

Dyspnea Abdominal Pain Malaise Sternal/Rib Pain CNS Changes Bleeding

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CBC Bone Marrow Aspiration Lumbar Puncture Genetic Analysis

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Chemotherapy Radiation Therapy Bone Marrow Transplant Peripheral Blood Stem Cell Transplant

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Risk for Injury: Infection, Bleeding Fatigue Impaired Oral Mucous Membranes Knowledge Deficit Anxiety

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Pathophysiology◦ Cancer of Plasma Cells in Bone Marrow◦ Tumors Devour Bone Tissue◦ Organ Invasion

Etiology◦ Unknown◦ Occupational Exposures

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Bone Pain Fever Malaise Spinal Cord Compression Pathological Fractures Hypercalcemia Infection

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CBC, Blood Calcium Bone X-Rays Urine for Bence

Jones Protein Bone Marrow

Biopsy

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Steroids Chemotherapy Control of Serum Calcium Radiation Stem Cell Transplantation IV Pamidronate (Aredia)

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Risk for Infection Risk for Injury

◦ Fracture◦ Complications of Immobility◦ Hypercalcemia

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Cancer of Lymph System◦ Presence of Reed-Sternberg Cells

Etiology◦ Viral ◦ Genetic ◦ Immune Dysfunction

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Painless Swollen Lymph Node Pruritis Pain Induced by Alcohol Fever Night Sweats Weight Loss Malaise

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Edema of Face and Neck Jaundice Nerve Pain Retroperitoneal Node Involvement Spleen, Liver, and Bone Involvement

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Biopsy◦ Lymph Node◦ Liver and Spleen◦ Bone Marrow

CT, Chest X-Ray Lung Bone Scan Lymphangiography CBC

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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

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Chemotherapy Radiation Therapy

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Impaired Comfort Activity Intolerance Risk for Infection Risk for Ineffective Coping

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Lymphoma Arising from B Cells and T Cells Absence of Reed-Sternberg Cells Etiology

◦ Some Viruses◦ H Pylori◦ Immune Dysfunction◦ Occupational Exposures

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Painless Lymph Nodes Enlarged Tonsils and Adenoids Other Signs and Symptoms Similar to

Hodgkin’s Disease

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Biopsy◦ Lymph Nodes◦ Tonsils◦ Bone Marrow◦ Liver◦ Other

Bone Scan CT, Chest X-ray,

IVP MRI, PET Scan Lymphangiography CBC Liver Function

Studies Serum Calcium

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Chemotherapy Monoclonal Antibodies Interferon Therapy Radiation Therapy Stem Cell Transplant

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Activity Intolerance Risk for Infection Risk for Ineffective Coping

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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 Reed-

Sternberg Cells◦ Poorer Prognosis

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Surgical Removal of the Spleen

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Baseline Labs Blood Transfusion if Necessary Vitamin K Baseline Vital Signs Teach Coughing and Deep Breathing

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Monitor for Bleeding Monitor Vital Signs Administer Narcotics for Pain Encourage to Cough and Deep Breathe and

Ambulate

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Bleeding Pneumonia Atelectasis Infection OPSI


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