Hematology Flashcards

1
Q

Nursing care of hemarthrosis

A

Ice pack, Non weight bearing, elevate affected limb to heart, immobilization, no PROM exercises until acute injury phase is done

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2
Q

Health promotion/ education for Hemarthrosis

A

sport choices (non contact), healthy weight and good fitness, normalization (chronic illness), use of prophylactic infusions

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3
Q

Patient education for hemarthrosis

A

teach venipuncture and factor administration, stress that f.a. is never delayed, avoid aspirin (motrin ok) physical activity and exercise is fine and encouraged when not bleeding (choose sports carefully)

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4
Q

Who is Hemophilia B named after?

A

Stephen Christmas, the first patient described outlining the symptoms of Hem B

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5
Q

Why do cells sickle (what causes the clinical symptoms)

A

blood viscosity and hemoglobin increases and causes cells to sickle

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6
Q

SCD labs

A

CBC – decreased HGB/Hct, increased reticulocyte count, increased WBC’s and platelets, increased total bilirubin, Kids with SCD usually “live” at a hgb of sometimes 6-7. will typically not be symptomatic

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7
Q

What is hemoglobin electrophoresis?

A

lack of HGB A

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8
Q

1 cause of death in SCD

A

infection

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9
Q

1 cause of hospitalization in SCD

A

vaso-occlusive crisis

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10
Q

SCD nursing care post splenectomy

A

PICU transfer, Immediate, conservative pRBC transfusion (<10cc/kg), Raise HGB to no higher than 8.0 to avoid autotransfusion, Pain management, Antibiotics, THESE CHILDREN MAY RAPIDLY DETERIORATE

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11
Q

Nursing Care in Vaso Occlusive Crisis

A

Hydration: 1.5 x maintenance (not for every type of crisis!)
Analgesics- Opioid/NSAID combo, Appropriate dose, Appropriate time intervals
Antibiotics if infection is suspected
Oxygen is not routinely given unless there is an increased O2 demand/hypoxia

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12
Q

Discharge Teaching for Vaso Occlusive Crisis

A

Assessment tools, Tapering PO analgesics, Side effects, Incentive spirometry, deep breathing, Tolerance vs addiction, Keep pain journal

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13
Q

Genetics in SCD

A

Autosomal Recessive- 25% chance of getting

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14
Q

Pain and Fever management for SCD- Pt ed

A

Monitor temp, give NSAIDs as needed, ATC regimen should be instituted, Usually Ketorolac (Toradol), Morphine, Motrin, Use PCA if needed, Use non pharmacological techniques as well (heating pads, guided imagery, distraction), Assess and reassess pain frequently, ADVOCATE, Monitor your own beliefs and LISTEN to your patient

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15
Q

Pain management in kids

A

Pharm and non pharm methods
Pharm- Opioids and NSAIDs
Nonpharm- Psychological, Behavioral, Physical (slide 64)
Adjuvant medications given to calm child

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16
Q

S&S of Anemia

A

Pallor, weakness, fatigue, decreased HGB, HCT, RBCs

17
Q

What is ITP

A

autoimmune destruction of platelets

18
Q

Lab data for ITP

A

Lab Data: low platelet count (< 20,000) & antiplatelet antibodies, normal Hgb, normal differential, normal bone marrow (only done if something else is suspected)

19
Q

Prognosis for ITP

A

usually good, most children recover with no long term consequences

20
Q

PT ed in Iron deficiency anemia

A

Give iron supplements with fruit, not with milk
Give liquid iron through a straw or perform oral care after administration
Monitor for constipation, pallor, weakness, fatigue

21
Q

Normal CBCs for kids

A

Normal hgb- 11-15
Normal Hct- 30-44%
Normal retic- 0.5-1.5%
Normal WBC- 4.5-11

22
Q

Parvovirus and staff education

A

Appears with Aplastic anemia, B19 titers are elevated
Staff- pregnant staff should avoid contact with these patients because infection can cause harm to the fetus

23
Q

Treatment of Beta Thalassemia

A

RBC transfusions, folic acid, chelation, splenectomy, BMT, cord blood, SCT
Gene therapy in the works
NO IRON

24
Q

Von Willebrand’s Nursing Care

A

Treatment is given pre-operatively with surgery/dental work or bleeding episodes
Desmopressin (DDAVP®)
vWF: FVIII concentrate (Humate P®)
Other Supportive Measures- Anti-fibrinolytics, Oral contraceptives, Topical hemostatic agents

25
Q

Management of nose bleeds

A

Teach pt/parent to manage nose bleed by leaning FORWARD and apply continuous pressure to tip of nose with thumb and forefinger for at least 10 minutes.
Avoid all temptation to pick or blow your nose after a bleed