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61 Cards in this Set
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White Blood Cells(Leukocytes)
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White Blood Cells (WBC)
Formed in bone marrow and lymphatic tissue Destroy foreign cells via phagocytosis and antibody production |
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Granulocytes
(neutrophils, eosinophils, basophils) |
Neutrophils
fight bacteria Eosinophils fight parasites responds to allergens influences the inflammatory process Basophils contain histamine activate the inflammatory response |
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Agranulocytes
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Participate in inflammatory and immune reactions
Monocytes (macrophages) First line of defense in inflammatory process Phagocytize large cells & necrotic tissue Important for chronic infections Lymphocytes Blast cells in bone marrow, spleen, thymus and other lymph glands and tissue Responsible for immune protection |
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T Lymphocytes (T cells, B cells, Nautral killer cells)
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T-cells
Made in thymus Cell mediated immunity (RT an antigen) B cells Humoral immunity “memory” cells that produce antibodies to specific antigens Natural killer cells kill certain type of tumor cells and viruses |
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What is Acute Lymphocytic Leukemia (ALL)
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Cancer is the 2nd cause of death <15 years
Leukemia malignant disease of bone marrow and lymph system ALL most common form of childhood cancer Peak onset 3-5 years of age 80% of cases of acute leukemia in childhood Etiology; Genetic abnormalities Philadelphia chromosome (↓ prognosis) Trisomy 21 = 20 x ↑ Risk Chernoble - Nuclear Radiation exposure Alkylating agents or certain chemical agents Virus trigger of oncogene |
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What is the ALL Pathophysiology?
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Abnormal, poorly differentiated blast cells
DNA mutation of an immature white blood cell Causes the cell to multiply uncontrollably Infiltrate bone marrow & ↑ vascular RE organs Hepatomegaly Splenomegaly Lymphadenopathy Malignant blast cells replace the functioning WBC’s in bone marrow causing: Anemia (↓↓ RBCs) Neutropenia (↓↓ WBCs) Thrombocytopenia (↓↓ Plts) |
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What are the ALL Signs and symptoms?
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1st sign: Infections that linger > 2 weeks (↓WBC)
Fever Chills Anorexia Weight loss (↑ metabolic demands of CA cells) Bone & joint pain (Marrow expansion) Abdominal pain (Hepatosplenomegaly) Pallor, fatigue, lethargy (↓ RBCs) Ecchymosis, petechiae, GI bleeding (↓ Plts) CNS = ↑ICP ( HA, Vomiting & Irritability) Late stage RT Brain protected by blood barrier. |
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How to diagnose ALL?
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Bone Marrow Aspiration @ iliac spine
>25% blast cells = + diagnosis Lumbar puncture (LP) √ any CNS involvement PET, CT & MRI Scans |
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ALL good prognosis?
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WBC <10,000/mm3
Age 1-10 Female Early + response No CNS involvement |
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ALL poor prognosis
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WBC >50,000/mm3
Age <1 or >10 Male Poor treatment response CNS involvement |
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Corticosteroids
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Anti-inflammatory
↓ and kill lymphoblastic cells (↓ WBC) Prednisone - 40 mg/m2 PO QD Dexamethasone – 2.5 -10mg/m2/day IM/IV ÷ q6-8H Side Effects: Hyperglycemia Na & Fluid retention = wt gain, puffy moon face Peptic ulcers, mood changes Delayed growth pattern |
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Enzymes
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↓ levels of amino acid (asparagine) →
↓↓ tumor growth L-Asparaginase (Elspar) 10,000 u/m2/day IM 2x/week Side Effects: Allergic rxn = chills, fever & rash Jaundice √ LFTs Respiratory distress & ↓ BP N & V, DM |
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Plant Alkaloids
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Anti-neoplastic = Inhibits cell division
Vincristine (Oncovin) 1.5 mg/m2 IV Side Effects Peripheral neuropathy severe constipation ↓ bowel innervation Stomatitis, N & V, Anemia Thrombocytopenia |
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Alkylating Agents
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Interferes with cell growth
Cyclophosphamide (cytoxan, CTX) 60-250 mg/m2/day Ifosfamide (Ifos) 1.2gm/m2/day Cisplatin (Platinol) 30-70 mg/m2/day Side Effects Alopecia Pulmonary fibrosis Hemorrhagic cystitis (caused by chemical irritation of drugs) Leukopenia Anorexia, N & V |
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Antibiotics
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Documented bacterial infections
Actinomycin D (dactinomysin, ACT-D) 2.5 mg/m2/wk Bleomycin (Blenoxane) 10-20 U/m2/wk Doxorubicin (Adriamycin) 20mg/m2/wk Side Effects Cardiotoxic! Red urine (Not hematuria) Alopecia N & V and stomatitis |
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CNS Prophylactic (Antimetabolites)
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Inhibits folic acid reductase = inhibits DNA synthesis and cellular replication. Inhibits replication of neoplastic cells
Methotrexate (MTX, Amethopterin) 20mg/m2/week PO IV or Intrathecal Mercaptopurine (6-MP) 75mg/m2/day IV Cytarabine (Ara-C, Cytosar-U) 100-200mg/m2/day IV 5-Fluorouracil (5-FU) 7-12mg/kg IV Side Effects Leukopenia, chills/fever, vomiting Red rash, Alopecia ↓ Folic Acid metabolism Hyperurecemia |
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Allopurinol (zyloprim)
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Inhibits production of uric acid.
CA cell destruction = ↑ uric acid levels accumulates in tubules → renal calculi Side Effects ↑ SGOT & SGPT = hepatotoxicity Blocks metabolism of 6-MP = 6-MP toxicity Need 1/3 -1/4 normal dose of 6-MP |
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Mesna (mesnex)
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Ifosamide detoxifying agent.
Binds to toxic metabolites. Prevents hemorrhagic cystitis Use with alkylating agents Cytoxan, Ifos, Platinol |
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Radiation
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Prophylactic in high risk patients
Minimize CNS involvement Side Effects after 7-10 days GI |
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What are the radiation side effects?
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Side Effects after 7-10 days
GI dysphagia, stomatitis, N & V, diarrhea Skin Erythema, desquamination, alopecia Myleosuppression ↓ RBCs ↓ WBCs↓ Plts Fatigue, Infection, Bruising/Bleeding Pneumonitis ↑ RR ↑HR Dyspnea & dry cough |
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What are Transfusions?
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Used to correct specific deficiencies
PRBC Epoetin (Epogen)/Procrit ↑ RBC in 2-6 weeks Platelets Granulocyte Colony Stimulating Factors-GCSF Filgrastin (Neupogen) ↑Neutrophils (ANC) Stimulate dev of new white blood cells 10-14 days SE: Bone pain, fever, malaise & HA Whole blood transfusions Rarely used since ↑ risk of fluid overload |
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What is a Bone Marrow Transplant?
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Replaces pt own bone marrow.
Need 500 cc -1 Liter Takes 1-3 weeks for marrow to self produce Autologous uses own bone marrow if in remission Allogenic (Donor) √ Compatible = match 6 HLA antigens Prevent Graft vs. Host Disease (GVHD) |
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What you have to do for a Bone Marrow Transplant?
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1st give ↑↑ dose chemo and radiation (total body)
Rids body of CA cells Suppresses immune system to prevent rejection Strict reverse isolation Neutropenic Precautions No fresh flowers, fruit, veggies Monitor visitors √ immunization status Monitor s/s of infection √ Temp, CBC, Activity √ Absolute Neutrophil Count (ANC) <500 ↑ risk for overwhelming infection ANC = WBC times the % of neutrophils |
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Nursing Interventions (prevent Infections)
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Live vaccines are contraindicated.
No MMR or Varicella Inactivated vaccines Wait @ least 6 months after chemo for appropriate immune response ↑↑ predisposition to resistant organisms Broad spectrum prophylactic antibiotics |
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Nursing Interventions (Nutrition)
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↑↑ Hydration ↑ Protein
↑Caloric Intake Bland , easily digestible diet Encourage nutritious foods Allow pt to choose ↑ Pt participation with meal planning No acidic juices or spicy foods |
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Nursing Interventions (Mouth Care)
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Frequent cleansing
Magic Mouthwash (Malox/Benadryl/HO) Cotton swabs not toothbrush for ↓ Plts Stomatitis Chloroseptic spray Viscous Lidocaine |
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Nursing Interventions (Skin Care)
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High risk for rectal ulcers from diarrhea
Keep area clean and dry & OTA Turn & Position Sheepskin or Air mattress √ SE from meds & radiation ↑risk for skin breakdown & irritation |
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Nursing Interventions (Nausea and Vomitting)
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Small frequent feeding
↑ PO intake via ices, jello, favorite fluids √ weight √ I and O’s Antiemetics Ondanesetron (Zofran) [Aloxy] Blocks 5-HT3 site in brain Dronabinol (Marinol) THC synthetic active component of marijuana |
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Nursing Interventions (Peripheral Neuropathy)
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↓ bowel innervation → constipation
Foot drop, tremors, jaw pain Weakness & numbness of extremities Maintain safe environment Assist with ambulation Sneakers, hand rails & walkers |
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Nursing Interventions (Alopecia)
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Prepare child & family ( temp condition)
Allow kids to cut their own hair! Obtain wig before hair is lost Scarfs or hats Re-growth 3-6months Darker, thicker & curlier |
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Nursing Interventions (Hemorrhagic Cystitis)
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Chemical irritation to the bladder
↑ Fluid intake (1.5 x daily amount) ↑ Voiding frequency Medication Mesna ↓ Urotoxicity of Ifos & Cisplatin |
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Nursing Interventions (Pain Relief)
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Evaluate non-verbal and verbal cues
Note cultural differences & accommodate needs |
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Nursing Interventions (Position)
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H2O beds
bean bag chairs stuffed animals |
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Nursing Interventions (Change Environment)
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↓ Sensory stimulation (lights, noise, activity)
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Nursing Interventions (Relaxation Techniques)
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Massages, rocking, guided imagery, distraction,
Humor! |
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Pain Meds
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Give ATC to maintain steady state
Give meds before pain is severe Adhere to scheduled med time Kids have ↑ BMR Need more frequent dosing not ↑ dose Tylenol [10-15 mg/kg/dose q 4-6 H] Maximum 90 mg/kg/dose (hepatotoxic) Tylenol with codeine [Codeine 0.5 -1 mg/kg/dose] Tylenol No. 1 (Codeine 7.5 mg & Acetaminophen 300 mg) Tylenol No. 2 (Codeine 15 mg & Acetaminophen 300mg) Percocet [oxycodone 0.1 mg/kg/dose] [Oxycodone 5 mg & Acetaminophen 325 mg] Tylox [Oxycodone 5 mg & Acetaminophen 500 mg] Vicodin [Hydrocodon 5mg & Acetaminophen 500 mg] |
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Pain meds NSAIDS & OPIOIDS
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NSAIDS
Ibuprophen (Motrin) 40 mg/kg/day SE: Skin rash, abdominal cramps, N, dizziness Opioids Hydromorphone (Dilaudid) 0.4 -1mg/kg q 4-6 H Quick onset of action 15 minutes Shorter duration than MSO4 ↑ potency 1 mg Dilaudid = 4 mg MSO4 Morphine SO4 (Roxanol) 0.025 -2.6 mg/kg/H SE: Sedation, ↓ RR ↓BP Constipation Flushed face Methadone (Dolophine) 0.2 mg/kg q 6-8 H Long ½ life 24 -36 H SE: Confusion, Sedation, ↓BP Constipation |
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Pain Meds Nursing Interventions
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Emotional support
Guidance with honest answers Education Serious signs & symptoms, adverse drug effects When to seek medical attention Establish good plan for FU care Encourage verbalizations or fears/ concerns Reassure pt will be comfortable |
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What is Neuroblastoma?
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Most common solid malignant tumor in kids
↑ risk < 2 years old. 75% before child is 5 years old. Tumors begin as embryonic cells Develop into the adrenal medulla and sympathetic nervous system (ganglia). Majority a non-familial, sporadic pattern Silent Tumor 70% Dx after metastasis Poor Prognosis |
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What are the clinical manafestations of neuroblastoma?
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Mediastinum (15%)
Compresses trachea & bronchi Tracheal deviation Persistent cough, Dyspnea & SOB Stridor & Chest pain Lymphadenopathy Cervical, supraclavicular & groin Neck/facial edema ↑ ↑ HA in AM & ↑ ↑ HC Supraorbital ecchymosis (Raccoon eyes) Infection Systemic Weight loss RT Anorexia RT ↓↓ Bowel function Irritability Fatigue Myoclonus ataxia syndrome Anemia Febrile, ↑ HR ↑ BP Changes in urination, bowel elimination |
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Signs That Diagnose Neuroblastoma?
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CT: Chest, Abdomen & Pelvis
Bone Scan IVP Abdominal Sonogram Bone Marrow aspiration and biopsy CBC: √Anemia √Thrombocytopenia 24 H urine collection of VMA Vanillylmandelic Acid = ↑ DA & NE |
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Neuroblastoma Treatment?
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Surgery if tumor is localized
Radiation ↓ size of tumor a & p surgery Chemotherapy Diffuse & advanced disease Cytoxin, Vincristine & Cisplatin 3F8 immunotherapy |
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What is Wilm’s Tumor (Nephroblastoma)?
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Common type of abdominal tumor
↑ Incidence with Hypospadias & Cryptorchidism 80% diagnosed at <5years ↑ risk @ 3 years 90% survival rate ↑ Cure rate with early diagnosis Encapsulated Tumor Arises from renal parenchyma Rapidly growing tumor Favors left kidney and usually unilateral 10% of cases have both kidneys involved |
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What are the Clinical Signs for Wilm’s Tumor (Nephroblastoma)?
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Non-tender mid-line abdominal mass
Flank pain ↑↑ BP RT kidney & adrenal compression & Renin Anemia RT Hematuria Rare Mets → Lung & Bone |
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Wilm’s Tumor (Nephroblastoma) Diagnose ASAP
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Abdomen & Chest
CT scan, X-Ray & Ultrasound IVP Renal function tests CBC with differential Bone scan |
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What is the therapy for Wilm’s Tumor (Nephroblastoma)?
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1st Place sign on wall:
DO NOT PALPATE ABDOMEN! Radiation and chemo a & p surgery Surgery Radical Nephrectomy whole kidney and adrenal Large Y autopsy-like incision: Examine entire abdominal cavity |
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What are Nursing Interventions forWilm’s Tumor (Nephroblastoma)?
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Prepare family for scar
Prepare for chemo and radiation Abdominal surgical care I&O’s Monitor bleeding No contact sports Watch for any kidney infections or ⇊ function |
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What is Osteogenic SarcomaOsteosarcoma?
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Arises from bone forming osteoblasts and bone digesting osteoclasts
Most common bone tumor in children 10 – 15 years, can go up to 25 years Femur, tibia or shoulder near growth plate ↑ Frequency during growth spurt |
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What are the Signs and Symptoms for Osteogenic SarcomaOsteosarcoma?
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Gradual onset
Insidious, intermittent local joint pain Palpable mass – (Bone Biopsy) Pain more intense with activity Limp & change in gait, ↓ ROM High serum alkaline PO4, and LDH Pathological fractures Starburst formation on x-ray |
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What is the Therapy for Osteogenic SarcomaOsteosarcoma?
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R/O Metastasis
Bone Scan, CT, MRI & Lung Scan Surgery Amputation 3” proximal to tumor or joint Limb salvage Chemotherapy ↑ Methotrexate, Adriamycin, Cisplatin, Ifos |
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Osteogenic Sarcoma Osteosarcoma Pre OP
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Exercise to strengthen upper arms
Prepare patient for extensive PT Emotional support allow pt to grieve for limb loss Focus on what the pt can do Support Group: ACS-Osteo Support Group; Camping & youth directed activities www.candlelighters.org |
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Osteogenic Sarcoma Osteosarcoma Post OP
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√ signs of hemorrhage q1H x 24 then q4H
Tourniquet at bedside (arterial bleed) Venous oozing reinforce dressing Pressure dressing Mold and shape for prosthesis Phantom limb pain Stimulation of nerve endings Burning, aching, tingling & cramping. It is real! Pain meds & Elavil |
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Osteogenic Sarcoma Osteosarcoma Post OP positioning
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1st 24 H - Elevate stump with pillow
>24 H No pillow below knee Position prone to prevent hip flexion No external rotation or abduction Place prosthesis immediately after surgery. Fosters early function and adjustment |
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What is Ewing’s Sarcoma?
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2nd most common malignant bone tumor
Highly invasive into bone marrow. Infiltrates soft tissue around the bone Pain with soft tissue mass Sites: Femur, tibia, fibula, ulnar, ribs and vertebrae 5 – 25 years of age (peaks @ age 10-20) Prognosis depends on degree of infiltration |
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What is Therapy for Ewing’s Sarcoma?
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Chemotherapy
Shrinks tumor & control mets VAC Vincristine, Actinomycin & Cytoxan Intensive Total Body Radiation (6-8 weeks) No Surgery – tumor is too invasive |
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What is Nursing Interventions for Ewing’s Sarcoma?
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Anticipatory guidance RT Therapy SE
Radiation burns Erythema, blisters, pain Hyperpigmentation Loose clothing, protective cream, Protect against sunlight Avoid sudden changes in temp No ice/heat packs |
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What is Non-Hodgkin’s Lymphoma?
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Malignancy of lymphatic system
Proliferation of T or B lymphocytes Lymphoblastic Lymphoma 30% 75% Medialstinal mass, Pleural effusion Lymphadenopathy Large B Cell Lymphoma 20% Lymphadenopathy & Invades other tissues Associated with Epstein Barr virus Small,non-cleaved type 50% Burkitts Lymphoma-90% (intrabdominal mass) Generalized and very aggressive ↑ Incidence with age Males 2x > females ↑ Incidence with AIDS |
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What are Signs and Symptoms of Non-Hodgkin’s Lymphoma?
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Acute onset & progression
Pain & swelling in chest or abdomen Lymphadenopathy in neck, underarm or groin Fever, malaise & Night Sweats Mediastinal mass = SOB ↑ RR ↑ Cough CNS = HA & vomiting (no nausea) Superior Vena Cava Syndrome (SVCS) Obstruction of SVC Edema of face, neck & trunk Bone Marrow Infiltration Petechia, Bruising, Bleeding & Bone Pain |
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What to Use to Diagnose Non-Hodgkin’s Lymphoma?
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Biopsy from tumor site
Staging (I – IV) Bone marrow & Lumbar puncture CT: Chest, Abdomen & Pelvis PET Scans (total body) ↑ activity & uptake Gallium Scans- Cardiac Tumor Lysis Syndrome (WBC > 50,000) Release of purines from destroyed lymphoblasts ↑ Uric acid levels →Renal Failure Therapy IV NaHCO3 keep urine pH > 7-8 Allopurinol (Zyloprim) ↑ uric acid secretion |
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What is the Treatment for Non-Hodgkin’s Lymphoma?
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Chemotherapy
Multi Agent aggressive R-CHOP protocol R= Retuxin (monoclonal AB therapy) CHOP Cytoxin, Adriamycin, Oncovin (Vincristin) & Prednisone Radiation 20 - 40 treatments @ tumor site |
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What are the nursing interventions for Chemo/Radiation & Immunizations for Non-Hodgkin’s Lymphoma?
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Chemotherapy & Radiation SE
Aranesp, Procrit, PRBC Transfusions Neupogen & Neutropenic Precautions No fresh fruit or Vegetables ↓ Exposure to infections Immunizations Flu, PPCV, Gamma Globulins, Acyclovir Leuprolide (Lupron) suppress ovaries |