Hematology Flashcards

(64 cards)

1
Q

Concepts of hematologic disorders

A

GAS EXCHANGE AND TISSUE PERFUSION
RBC = delivers oxygen (hemoglobin)
— heme needs iron to transport oxygen
— four molecules of O2 can attach to heme

Someone with 100% SPO2 reading -> how many molecules are attached to the heme

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2
Q

Anemia

A

Reduction of RBC, hemoglobin and/or hematocrit
Classifications:
— blood loss
— hemolytic
— impaired RBC production

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3
Q

Types of anemia

A

Iron-deficiency (microcytic)
— blood loss, poor nutrition

Hemolytic
— immune
— trauma
— sickle cell

Megaloblastic (macrocytic)
— vitamin B12 deficiency
— PERNICIOUS ANEMIA
— folic acid deficiency

Aplastic anemia
— bone marrow suppression

Chronic
— chronic renal failure
— kidneys no longer produce epogen

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4
Q

What are CM of anemia?

A

— fatigue
— dizziness
— possible fainting
— hypotension
— hypovolemia
— high HR -> dysrhythmias
— chest pain -> low oxygen delivery
— SOB
— yellowing of the eyes in colored persons

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5
Q

Sickle cell anemia

A

Genetic
RBC in sickle shape (C shape)
— decreased oxygen carrying capacity
— abnormal hemoglobin
— C’s clump together very easily -> occludes blood vessels
— organ damage
— PULM EBOLISM, MI, stroke, kidney disease

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6
Q

Clinical manifestations of sickle cell anemia

A

— retinopathy
— cardiomegaly
— CHF
— hematuria
— stroke
— pneumonia
— splenomegaly
— ulcers on extremities
— osteomyelitis

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7
Q

Triggers for sickle cell

A

— HYPOXIA
— high altitudes
— dehydration
— venous stasis
— physical/emotional stress
— anesthesia
— infections
— low or high body temp

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8
Q

Medical surgical tx for sickle cell

A

— PAIN MANAGMENT
— opioids -> constipation
— hydration to keep cells from clumping
— OXYGEN
— prevent infection
— do not bend over -> RBCs can clump
— blood transfusion (hgb <7.5)
— hydroxyurea -> reduces sickling -> CAN INCREASE CANCER RISK FOR INFANTS (make sure female is not pregnant)

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9
Q

Teaching for sickle cell

A

— prevent crisis -> STAY HYDRATED; stay oxygenated
— manage drugs -> women on birth control taking hydroxurea
— emotional support -> will have disease for rest of life

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10
Q

Education for hydroxyurea

A

Do not get pregnant
Risk for infant cancers

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11
Q

Sickle cell nursing dx and interventions

A

Nursing dx:
— acute pain
— ineffective peripheral tissue perfusion
— deficient fluid volume
— activity intolerance
— risk for decreased cardiac tissue perfusion
— risk for infection
— risk for ineffective cerebral tissue perfusion

Nursing interventions:
— admin OXYGEN
— admin pain medications
— do not bend the client -> restricted blood flow/clumping of sickle RBCs
— check circulation of peripheral extremities
— assess signs of central claudication
— keep pt warm -> NO HEATING PADS
— admin IV fluids and PO fluids

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12
Q

Generalized anemia

A

— complete blood count with diff and RBC indices
— reticulocyte count
— iron studies
— coomb’s test -> hemolytic anemia / looks for antibodies on surface of RBC
— bone marrow aspiration -> looks to see if there is anything preventing RBC production

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13
Q

Normal range for RBC
What does decreased/increased lab indicate

A

4.2-6.1

Decreased = anemia or bleeding
Increased = severely dehydrated or PV

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14
Q

Normal range for hemoglobin

A

12-18

Deceased = anemia, bleeding, fluid overload
Increased = severely dehydrated

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15
Q

Normal range for hematocrit

A

37-52%

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16
Q

Medical surgical tx for anemia

A

— determine underlying cause
— iron deficiency -> oral ferrous for mild anemia (take with food - hard on the stomach)
— vitamin C enhances absorption of oral ferrous

Severe: IV or IM dextran
— check BP
— tele monitoring

Vitamin B12
— diet
— oral supplments

Blood loss
— stop bleeding
— mass trauma

Immune
— transfusion
— bone marrow transplant
— immunosuppressive therapies
— HIGH RISK FOR INFECTION

Chronic disease
— procrit/epogen injections to help stimulate erythropoietin

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17
Q

Assessment for anemia

A

— diet
— meds

CM:
— FATIGUE
— pallor
— cyanosis
— jaundice -> hemolytic anemia
— bleeding
— dry skin
— mouth ulcers or fissures
— smooth tongue
— lymph node involvement -> infection/cancer
— tachycardia -> low blood volume
— VS -> O2 saturation (carbon dioxide/monoxide poisoning the SPO2 will not be accurate)

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18
Q

Nursing dx for anemia

A

— activity intolerance
— fatigue
— altered tissue perfusion
— impaired gas exchange
— anxiety
— impaired comfort
— risk for bleeding
— risk for injury
— impaired memory

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19
Q

Interdisciplinary interventions and nursing interventions for anemia

A

— oxygen
— oral or IM iron
— supplments -> VITAMIN B, FOLIC ACID
— epoetin SQ weekly
— RBC transfusion for hgb <7.5

Nursing interventions:
— energy conservation
— supportive care
— correct anemia -> diet changes
— teaching self care

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20
Q

Level of hemoglobin that indicates need for blood transfusion

A

<7.5

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21
Q

Primary polycythemia Vera

A

Loss of cellular regulation
— RBCs, WBC and platelet
— blood will become viscous (THICK) -> poor oxygenation
— HIGH HEMOGLOBIN AND HEMATOCRIT

Hyperkalemia, high hct + hgb, high uric acid

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22
Q

CM and complications of polycythemia Vera

A

CM:
— HTN
— headache
— dizziness
— itching
— dyspnea
— purple/gray color

Complications:
— angina
— claudication -> stopping of oxygen/clotting
— thromboses
— infarctions -> MI, CVA
— intracranial bleeds/CVA FROM HTN

Medical tx:
— ANTICOAGULANTS

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23
Q

Nursing interventions for primary polycythemia Vera

A

— prevent clots = get up and ambulate as frequently as possible
— HYDRATION -> 3L/day
— stop smoking
— promote venous return
— elevate feet to prevent pooling in lower extremities
— avoid tight clothing
— support hose
— thrombocytopenia precautions -> bleeding precautions
— use electric razor, soft toothbrush (anticoagulants)
— neutropenic precautions -> higher risk for infection

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24
Q

Primary polycythemia Vera education

A

— contact doctor first sign of infection or occlusion
— exercise slowly
— stop activity at first sign of chest pain or dizziness (possible MI)
— interdisciplinary -> anticoagulants, chemotherapy to thin down/stop overproduction

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25
Nursing dx PPV
Ineffective protection Risk for bleeding Risk for ineffective tissue perfusion
26
Myelodysplastic syndrome (MDS)
PRECANCEROUS STATE — abnormal cell formation in bone marrow — destroyed by body after release; decrease in all blood cell types — Pancytopenia — 30% develop leukemia Risk factors: — >65 age — exposure to chemicals — tobacco smoke — chemo/radiation
27
Diagnostics for myelodysplastic syndrome
— cytogenetic testing -> looks at chromosomes that are identified as abnormal — peripheral blood smears -> cell abnormalities Medical tx: — supportive care — blood/platelet transfusion — epogen injections
28
Platelet disorders
— local bleeding-petichiae — easier to control — Idiopathic thrombocytopenic purpura -> immune system destroys platelets — Thrombotic thrombocytopenic purpura -> platelets clump together and forms clots
29
Clotting disorders
— occurs deeper in the body — bleeding in joint spaces; SQ — deeps bleeds difficult to control and often restarts — hemophilia — heparin-induced thrombocytopenia
30
Reasons for platelet disorders
Decreased production — cancers and tx — aplastic anemia — toxins; meds, alcohol Increased destruction — autoimmune — infections, meds, spleen disorder, cancers Increased consumption — disseminating intravascular coagulation - body is running out of platelets
31
Normal platelet count
150,000-400,000
32
Thrombocytopenia
TOO FEW PLATELETS — 40,000-80,000 platelets — risk for bleeding with mild trauma <20,000 risk for spontaneous bleed <5,000 risk for fatal bleed in CNS or GI hemorrhage Idiopathic thrombocytopenic purpura
33
Thrombocytosis
TOO MUCH PLATELET — platelets >60,000 — risk for clotting Thrombotic thrombocytopenic purpura
34
Idiopathic thrombocytopenic purpura
Autoimmune disorder — patients makes antibodies against own platelets — macrophages destroy Viral infections thought to trigger condition Most common in women 20-40 Dx: serial law platelets and bone marrow biopsy — shows bone marrow is putting out normal rate — body is chewing it up (platelets) Tx: — immunosuppressive drugs (prednisone) — platelet transfusion — splenectomy -> last resort
35
Thrombotic thrombocytopenic purpura
Autoimmune disease — platelets clump together abnormally in capillaries and too few available in circulation — clotting occurs but also fails to clot when trauma occurs — tissue becomes ischemic -> kidney failure, MI, CVA — FATAL IN 3 MO. IF NOT TREATED Tx: — plasmaphoresis — fresh frozen plasma to provide platelet aggregation inhibitors — platelet inhibitor drugs
36
Hemophilia
Genetic disorder — chance of giving disorder to offspring — women carrier Types: A = factor 8 (VIII) — 80% B = factor 9 (IX) — 20% Symptoms: — abnormal bleeding to any trauma, specifically joints — bleeding longer than normal — problem forming stable fibrin clot -> allows for extensive bleeding
37
PT range
11-12.5 Warfarin therapy Liver failure
38
INR range
0.8-1.1
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PTT range
60-70 seconds Heparin therapy
40
Medical and nursing management of hemophilia
Complications most common -> joint problems from repeated episodes of bleeding Dx -> prolonged PTT Tx -> replace missing factor with infusion of synthetic factors
41
Nursing management of hemophilia
Minimize trauma and other causes of bleeding — thrombocytopenia precautions — risk assessment -> protect pt from injury Assess s/s bleeding Prepare to admin platelet infusion for counts below 10,000 — replace missing clotting factors with transfusion of synthetic factors — educate patient and family -> risk for bleeding
42
Cancers of the blood
— leukemia — lymphoma — multiple myeloma
43
Leukemia
Uncontrolled NORMAL cell production — cancer occurs in stem cells of bone marrow -> overcrowded with nonfunctional cells Overproduction of blasts cells -> immature WBC Exact cause unknown — genetic and environmental factors involved — 50% of pt have abnormal chromosomes Normal cell production decreased results in: — Pancytopenia — neutropenia — anemia — thrombocytopenia — infiltration of tissue/organs
44
Acute leukemia
Sudden onset of abono al blood cells
45
Chronic leukemia
Abnormal cells replicate slowly
46
How is leukemia classified
By cell type — lymphoid cells: lymphocytic — myeloid cells: myelogenous
47
Types of leukemia
Acute lymphocytic leukemia — most common type in young children Acute myelogenous leukemia — most common type in adults Chronic lymphocytic leukemia — most common chronic adult leukemia Chronic myelogenous leukemia — asymptomatic for years enforce entering fast growth phase
48
Leukemia risk factors
— prior exposure to chemo or ionizing radiation — bone marrow hypoplasia (slow growth) — genetic -> Down syndrome — immune deficiency — virus
49
Definitive test for leukemia
Bone marrow biopsy
50
Leukemia dx
Abnormal WBC — high blast cells -> poor prognosis — low hgb + hct — low platelet Chromosome analysis X-ray, CAT scan, MRI
51
Clinical manifestations of leukemia
Systemic: — weight loss — fever — frequent infections Psychological: — fatigue — loss of appetite — SOB — weakness (lack of oxygen) — pain/tenderness in bones/joints — lymph node swelling — spleen/liver enlargement Skin: — night sweats — easy bleeding and bruising — purplish patches or spots
52
Nursing interventions for bone marrow aspiration
— provide info to pt about blood cells and production Nursing: — prone or side lying position — sedatives — needle and incision will be made Follow-up care: — control bleeding — inspection of site q2 hr — pain control
53
Medical tx of leukemia
Induction therapy — started as soon as dx confirmed — hospitalized 2-3 wk in protective isolation S/S: — severe bone marrow suppression — alopecia — n/v — stomatitis — organ toxicity Consolidation therapy: once recovered — repeat drugs or bone marrow transplant Maintenance: — months and years to maintain remission
54
What are the two main types of lymphomas?
Hodgkin’s lymphoma — teens and adults in 50s-60s Nonhodgkin’s lymphoma — all other lymphomas — over 60 types — older adult men
55
Hodgkin’s lymphoma
Starts in single lymph node in neck, underarm, or chest — proceeds in orderly fashion to next — fatigue, anorexia, SOB — sweats, fever, itching, weight loss — pain in node areas after alcohol intake
56
Risk factors and tx of Hodgkin’s lymphoma
Risk factors: — viral infections — chemical exposure Tx: — external radiation and chemo — CURABLE
57
Non-Hodgkin’s lymphoma
CHRONIC/NOT CURABLE — lymphadenopathy in multiple sites — spreads to other organs by the time of dx Risk factors: — autoimmune — immunosuppressive disorders -> HIV — chemicals Tx: — chemo/monoclonal antibodies — radiation — not curable
58
Multiple myeloma
Overgrowth of plasma cells — plasma cells overproduce gamma globulin (gammopathy) — excess antibodies in blood CLOG BLOOD VESSELS of KIDNEY and other organs -> infects the organs Produces excess cytokines — increase cancer growth rate and destroy bone Dx testing: — serum electrophoresis test detects monoclonal immunoglobulin (high levels of calcium) — bone marrow -> greater than 10% infiltrated plasma cells — X-ray -> osteolytic bone lesions
59
Early s/s of multiple myeloma
— fatigue — anemia — easy bruising — bone pain — infections
60
Late s/s of multiple myeloma
— bone factures — kidney dysfunction — HTN — RARE: hypercalcemia, hyper viscosity syndrome Leads to progressive bone destruction, bleeding, kidney failure, immunosuppression and death
61
Treatment and nursing interventions of multiple myeloma
Tx: — chemo agents — bone marrow transplant — INCURABLE Nursing: — care of immunocompromised patient — pain control
62
Nursing care for leukemia, lymphoma and multiple myeloma
INFECTION PROTECTION — prophylactic drugs -> antiviral, antibiotic, anti fungal — neutropenic precautions — monitor labs daily — monitor for early manifestations of infection — hygiene/skin care THROMBOCYTOPENIC PRECAUTIONS (bleeding precautions) — energy conservation — teach self care -> avoid large crowds — psychosocial support
63
Neutropenic precautions
Infection protection — avoid crows, children, ill people — wear mask — hand hygiene — good personal hygiene, mouth care — avoid constipation — shave with electric razor — do not handle feces — NO FRESH FLOWERS OR GARDENING — no invasive procedures — no sexual relations — no fresh fruits/veggies, raw meat, eggs, cheese — assess temperature
64
Thrombocytopenic precautions
Bleeding precautions — assess for s/s of bleeding -> bruises/nose/gums/urine/stool/severe headache — avoid IM/SQ/IV or invasive procedures — NO ASPIRIN/NSAID — soft toothbrush — no flossing/dental procedures — no razor blades -> electric — stool softeners to prevent straining — hold pressure for 5 min on venipuncture sites — teach s/s of bleeding — avoid situations where falls may occur