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Blood Disorders

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Question
Answer
Sickle Cell Anemia   Have BOTH defective gene **if you only get one you are a carrier  
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  Abnormal Hbg molecule= Hgb S= causes cells to sickle  
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complication of sickle cell anemia   cells cannot move through the blod vessls- they get stuck bc of shape  
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caused by   dehydration, stress, poor nutrition, vessels become clogged or blocked= tissue hypoxia  
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  death usually occurs from tissue damage to major organs  
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S/S   pain in bones/organs, fever, anemia, clots in lungs or spleen/spleenomegaly, edema, leukocytosis, chest/abdominal pain, D. ulcers  
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Positive screening of Hgb   get immunized, stay rested= reduce the amount of o2 demand for body, rest, eat well, regular check ups  
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PRIORITY for sickle cell anemia patients   PAIN CONTROL-- while in hospital- give Pain med and IV fluids-- may be "fequent fliers"- give apin meds promptly - pain will be over whelming  
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unique manefestation on Sickle cell anemia   Acute chest syndrom  
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  constantly check for HF R or L  
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  coughing, wheezing, techypnea, chest pain Jaundice - due to increase rate of RBC destruction Gallstones - from increase bilirubin  
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  risk for infection compromises growth Priapism-- increased time for an erection  
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when blood flow is reduced the patient will experience   localized ischemia, severe pain, tissue infarction, fever, pain, swelling  
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  treatment is surrpotive rather than curative regular blood transfusion Narcotics Oxygen Hydration  
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Hemolytic Anemia   chronic premature destruction of RBCs (erythrocytes) iron and Hgb are released  
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caused by   autoimmune reaction radiation blood transfusion (maily if you get the wrong blood) arsenic & lead poisoning medication  
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S/S - may go unnoticed or a sudden, severe reaction may occur   mild fatigue, pallor, jaundice, palpitations, hypotension, dyspnea, back & joint pain-- wrong blood  
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Treatment and Interventions   Find and fix UNDERLYING cause Blood transfusion Erythrocytoapheresis- procedure that removes abnormal RBC and replaces them with healthy RBCS Splenectomy- surgical removal of spleen Corticosteroids- decrease autoimmune response  
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  folic acid- increases production of RBCs  
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Pancytopenia   Numbers of ALL marrow-produced blood cells are reduced  
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Aplastic Anmeia   inadequate stem cell production in bone marrow possible autoimmune DEATH RATE IS HIGH  
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Assessment finding   infections (low WBC) coagulation abnormalities (low WBC) small skin hemorrhages (low platlets) enlarged spleem  
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Nursing Managmetn   watch for s/s of infection, assess temp, vitals, monitor for bleeding HISTORY  
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Pernicious Anemia   VIT B 12 deficieny- injections daily for 2 weeks then one per month for rest of life No cure but treatments are available for pt to have normal life span  
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Caused by   partial or complete removal of the fundus of the stomach (gastrectomies)  
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source of the intrinsic factor which is necessary for absorption of B12   fundus  
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Necessary element in the production of RBC and NS function   VIT B 12  
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immature RBCs   large and die quickly  
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labwork will show   low RBC Hgb low High Bili- jaundice  
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Cardinal sign   tounge in sore and beefy red- toung is very vascular  
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the more Neurological problems   the worst the Anemia is (tingling of hands & feet, loss of body position, memory loss, confusion, depression, if NOT treated- partial or total paraylsis  
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Diet   high in protein, vitamins, minerals  
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  B12 has no side effects & cannot overdose  
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Folic Acid Def   low folic acid levels -- Treatment-- VIT C- helps with maturity of RBC and absoption  
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Foods with Folate:   breads, cereals, green leafy vegies, orange juice, dried peas and beans  
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Polycythemia Vera (Erythrocytosis)   abnormal production of RBCS, WBCS, PLTS RBC count may range from 7-10 mill-- (norm is 3.6-5.4)  
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  oxygen content of blood is diminished due to short life span of RBCS Blood flow rate is slowed due to increased thickness-- increased risk for clots  
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  HTN- bc H blood vol- thick blood CVA- clotting factors H CHF- too much blood hemorrhage- at risk bc amount H amount of Blood  
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S/S   Angina(most common), HA, fatigue, Night sweats, Puritis, Dyspnea, enlarged spleen/liver, skin bruising, bleeding mucous membranes  
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Treatment- Objective- Supress bone marrown, decrease blood cell mass, reduce # of RBCS, WBCS, PLTS   chemo to suppress bone marrow phlebotomy- reduce excess volume (sv x wk) high risk for developing Leukemia  
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  high fluid intake- help prevent clots restriction of blood flow- no tight cloths' encourage isometric exercise if angina - educate patient to REST  
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Position to put pt in with enlarged spleen   sitting position  
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Lymphatic System   a network of vessls that transport lymph (watery fluid from plasma that exits the walls of capillariers and enters interstitial space)  
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ALWAYS   check tonsils for size & enlargement  
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lymphocytes & macrophages   trap destroy remove (why our lymph nodes are swollen)  
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Primary lymphemdema   congenitally acquired/ Affects women more that men (mastectomy)  
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Secondary Lymphedema   develops from complications of other disorders, removal of mult lymph nodes  
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  Parasitic worm-- Most common cause of Lymphedema -- always ask about forgien travel (secondary)  
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when the volume of lymph exceeds the capicity of the vessels- lymph enters interstitial space w/in soft tissues   trapped fluid eventually causes non-pitting edema  
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  RESULTS FROM IMPAIRED LYMPH CIRCULATION  
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nursing management for Lymphedema   assess affected area, elevate extremity, encourage movement, support, teach about garments and mechanical devices  
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Treatment   symptomatic  
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Lymphangitis, Lymphadenitis   Strepococcal microorganisms  
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  red streaks-fever-tender-enlarged lymph nodes Visual inspection and Palpation  
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PAIN managment   note the respose to antibiotic therapy- decrease redness, swellilng, elevate extremity, apply warm soaks to area  
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  BROAD SPECTRUM ANTIBIOTICS  
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Infectious Mononucleosis   Epstein-Barr Virus Direct contact secretions  
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  Fatigue, Fever, sore throat, cervical lymph enlargement, oozing tonsils, pharyngeal swelling  
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Epstein-Barr virus can cause lyphoma bc   of the way it attacks the body  
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AViod blood donation for   6 months  
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Hodgkins Disease   Reed Sternberg cells onset 15-40 and then older than 55 orderly growth more curable  
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Non-Hodgkins   NON-reed sternberg cells Genetic - Aggressive peaks after 50 30 subtypes B&T cell origins Mets common Less curable  
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Leukocytosis   increase in WBC sign of infection more indicate leukemia usually accompany fever  
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common s/s of leukemia   anemia, weakness, fatigue  
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  definite cause is unknown- toxic chemicals, radiation, viruses, certain drugs, genetics  
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ALL   occurs primarily in children  
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AML   Affects all age ranges  
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CLL AND CML   CLL- commonly affects those older than 40- MOST COMMON in adults CML- found in those older that 20- incidence increases with age- 95% genetic link  
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  in ALL leukemias- there is risk of infection  
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ecchymosis   bruising  
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petichia   tiny red dots  
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purupa   redish/ purple small skin hemorrhages  
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most of the pt discomfort results from treatment than the disease   chemo/radiation  
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normal platlet count   150,000-350,000  
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WBC   5,000-10,000  
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if you have cancer and you are anemic   you will recieve a blood transfusion  
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treatment of choice if remission occrs   Bone Marrow Transplant  
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Multiple Myeloma   Cause is unkown CANCER OF THE plasma cells - results in abnormal production of immunoglobulins Abnormal plasma cells cannot protect the pt  
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PLASMA CELLS   destroy bone & lymph nodes, liver, spleen and kidneys  
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  symptoms occur when kidneys are damaged or infection sets in Pathological FX RENAL CALCULI  
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HOW MUCH FLUID   3-4 L unless contraindicated  
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Agranulocytosis Caused by adverse reaction to...   Butazolidine, Choloromycetin, Penicillin & its derivatives, Dilantin, Onocovin, Diuretics, Thorazine, Sulfa CELEBREX  
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  Neoplastic disease- cancer causing  
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  chemotherapy, radiation, bacterial and viral infections  
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RESULTS IN   bone marrow suppresion- thus reducing WBC pro # of granulocytes are severly reduced  
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s/s   HA, fever, chills(BAD-chills cause body heat=fever)Fatigue Mucous membrane ulceration of the...  
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  nose, mouth, pharynx, vagina, rectum  
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MAIN GOAL   remove cause of bone marrow supression prevent or treat infection  
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  blood transfusion- provide mature wbc to wk system  
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protective isolation   due to low WBC- reverse or neutropenic  
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diet   soft, bland, high in calories, protein, vitamins  
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Aplastic Anmeia   bone marrow shuts down completely severe life threatening very poor DX  
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ppl on chemo have blood drwn   everyday for labs  
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1st sign of organ rejection   FEVER  
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thrombocytopenia   decrease inPLT count related to  
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  aplastic anemia, tumors, leukemia, chemo  
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platelet survival rate is also lowered due to   infection or viral illness  
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