Clinical Care of the Hematologic System Flashcards

1
Q

What is usually the cause of iron deficiency in adults?

A

bleeding

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2
Q

how is anemia defined in regards to hematocrit levels with adult males and females?

A

less than 41% (Hemoglobin 13.5g/dL) in Males

less than 37% (hemoglobin 12g/dL in Females

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3
Q

what are the symptoms/PE findings of of anemia?

A

lymphadenopathy, hepatosplenomegaly, or bone tenderness.

Mucosal changes such as smooth tongue suggests megaloblastic anemia

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4
Q

What labs would you do for anemia?

A

CBC with diff
Iron with total iron biding capacity (TIBC)
Microscopic analysis
Hemoglobin electrophoresis

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5
Q

what will be your findings on TIBC for anemia?

A

Ferritin value <12 mcg/L indicates iron (Fe) deficiency anemia

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6
Q

what is the treatment if the cause of anemia is not identified?

A

referral to internal medicine

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7
Q

What are some of the specific anemias?

A

Iron Deficiency Anemia

Vitamin B12 Deficiency

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8
Q

Physical exam findings of Iron deficiency anemia?

A

fatigue, tachycardia, palpitations, tachypnea on exertion.

smooth tongue, brittle nails, cheilosis. dysphagia, and pica (craving foods not rich in iron, like ice chips).

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9
Q

What is the most important treatment with anemia?

A

identification of blood loss….

after Oral Iron (ferrous sulfate, 325 mg, 3x day, 3-6 months)
or parenteral iron (dosage derived by hematologist)

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10
Q

What are the essentials of diagnosis for Vitamin B12 Deficiency?

A

hype segmented neutrophils on peripheral blood smear.
Serum B 12 < 100pg/ml

Hallmark is megaloblastic anemia (large RBCs)

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11
Q

vitamin b12 deficiency normally develops more than how many years after vitamin b 12 ceases?

A

3 years.

because the body has 2000-5000 mcg of b12 stored.

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12
Q

what population is most likely to see B12 deficiency?

A

vegans

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13
Q

what are some rare causes of b12 deficiency?

A

fish tapeworm
pancreatic insufficiency
Severe Crohn disease that destroyed much of the ileum

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14
Q

physical findings of B12 deficiency?

A

glossitis
anorexia
diarrhea
late stages will be pale, w paresthesia and difficulty w balance

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15
Q

what is the hallmark of Vitamin B 12 deficiency?

A

megaloblastic anemia on CBC with diff.

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16
Q

What is the treatment of Vitamin B12 deficiency?

A

IM injection of B12. Daily for a week, Weekly for a month, monthly for life.

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17
Q

three stages of blood clotting?

A

Formation of prothrombinase
prothrombin into thrombin
thrombin converts soluble fibrinogen into insoluble fibrin threads

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18
Q

Hemophilia A is a congenital deficiency of which coagulation factor?

A

VIII

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19
Q

Hemophilia B is a congenital deficiency of which coagulation factor?

A

IX

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20
Q

what is a condition where the process of coagulation and fibrinolysis become abnormally activated within the vasculature, leading to ongoing coagulation and fibrinolysis?

A

Disseminated intravascular coagulation (DIC)

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21
Q

what are some manifestations of DIC?

A

petechia, ecchymoses, blood oozing from wounds.

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22
Q

causes of DIC?

A

sepsis
malignancy
obstetrical complications
intravascular hemolysis

less common, but seen in heat stroke, crush injuries and rattlesnake and viper bites.

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23
Q

what medications would you give for DIC?

A

heparin

coumadin

24
Q

symptoms of DIC

A

bruising
epistaxis
bleeding from eyes
heavy vaginal bleeding

25
what drugs could cause a episodic hemolytic anemia in patients with g6pd?
Primaquine, aspirin, ciprofloxacin
26
what do you call the "bite" cells that appear in patients with g6pd under oxidative stress?
Heinz bodies.
27
how do you see heinz bodies on a blood smear?
stain with Cresyl Violet or they will not be visible.
28
Symptoms/Physical Exam findings of Sickle Cell:
jaundice, pigment, gallstones, hepatosplenomegaly, and poor healing ulcers over the lower tibia non healing ulcers in the lower ley. cardiomegaly painful episodes in the bones (especially long bones and chest) low grade fever
29
if you have Sickle Cell Trait, you are clinically normal, but what can cause acute painful episodes?
extreme conditions such as vigorous exertion at high altitudes (or in unpressurized aircrat)
30
what percentage of blasts will be in the bone marrow with acute leukemia?
20%
31
two classifications of acute leukemia?
Acute myeloid leukemia (AML) is an adult disease with median age of 60 years old. Acute Lymphoblastic leukemia (ALL) 80% in childhood and 20% of adults.
32
You will have blasts in what percentage of acute leukemia patients?
90%
33
vast majority of AML patients are diagnosed at what age?
20
34
symptoms of acute leukemia
fatigue bleeding on mucosal surfaces, gingival bleeding, epistaxis, menorrhagia infection gum hypertrophy and bone and joint pain patients may appear peale and have petechia. enlarged liver, spleen, and lymph nodes sternum, tibia, and femur tenderness
35
DDX of acute leukemia
mono pertussis anemia hypothyroid
36
what is the hallmark of acute leukemia with labs/studies/EKG?
pancytopenia with circulating blasts patients with ALL may have mediastinal mass visible with x ray
37
what percentage of blasts is required to make a diagnosis of acute leukemia?
20%
38
How many achieve remission with AML diagnosed under 60 years old?
70-80%
39
what is a high white cell count called?
leukocytosis
40
what is a low white cell count called?
leukopenia
41
what are some etiologies of neutrophils leukocytosis?
bacterial infection inflammation metabolic disease stress
42
what are some etiologies of lymphocyte leukocytosis?
viral infection immune disease stress leukemia
43
what are some etiologies of eosinophil leukocytosis?
skin disease drug reaction parasite infection asthma
44
what are some etiologies of basophil leukocytosis?
chronic myeloid leukemia
45
signs and symptoms of leukocytosis or leukopenia are varied and depend on underlying cause. name some
``` Infectious symptoms: fever skin erythema, ulcerations, fissure, gingivitis, swelling, oral ulceration dental pain abnormal respiratory exam ``` Other findings: jaundice joint pain
46
how do you determine the cell being affected with either leukocytosis or leukopenia?
CBC with diff
47
what is the disease with abnormally low amount of circulating platelets?
thrombocytopenia
48
the risk of spontaneous bleeding with thrombocytopenia does not increase until the platelets fall below what range?
10,000 to 20,000 /mcl
49
potential causes of thrombocytopenia?
``` bone marrow failure DIC chemo nutritional deficiencies bone malignancy meds ```
50
symptoms of thrombocytopenia
Petechia*** | mucocutaneous bleeding
51
treatment for thrombocytopenia?
stop offending medications evaluate for cause refer to internal medicine or hematologist MEDEVAC
52
What is thrombocytosis?
abnormally high amount of circulating thrombocytes n(450,000)
53
what are the two different categories of thrombocytosis?
Reactive- anemia, blood loss, infection, inflammation, post splenectomy Autonomous- primarily cancers of bone marrow
54
symptoms of thrombocytosis?
``` 50-60 years of age elevated platelets increased risk of thrombosis erythromelagia- painful burning of hands with erythema splenomegaly in 25% of patients ```
55
Treatment for thrombocytosis?
refer to hematology if there is no infectious cause and does not resolve in 2-4 weeks