Sasha: Clinical Assessment Heme/Onc Flashcards

1
Q

Blood Draw:

Adult site

Infant site

A

Adult sites: Cubital fossa, medial vein

Infant sites: Heel, Scalp

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2
Q

Is a venipuncture clean or sterile?

A

well… it depends -usually? CLEAN so what does this mean? use alcohol prep…start on the inside making circular motions and work your way out cleaning the site. when would we do sterile blood draw? transfusions/blood culture so that way you don’t introduce bacteria into the sample

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3
Q

When would you want an arterial sample?

A

BLOOD GAS you order these when your patient has an altered mental state you want to know how much oxygen is in the brain

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4
Q

What is anemia?

A

Disorder of RBC there are numerous types and etiologies

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5
Q

what symptoms do all anemia’s share?

A

All share fatigue and pallor as symptoms

why do you have these symp? Lack of oxygen to body tissues

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6
Q

what is pallor? and where do you look for it on the body?

A

Pallor= pale Look for this in conjunctiva mucosa and on skin of hands and nails—can mean low anemia

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7
Q

what (at minimum) lab work do you do for anemia

A

CBC with differential

Peripheral blood smear (usually), shows morphology of RBC

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8
Q

What does CBC stand for?

A

Complete blood count

I know you got this one….good job!!!!!

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9
Q

what is the difference between a CBC w/ differential and a CBC without differential and what does a CBC include?

A

Differential- gives more information…more to interpret..

all the different types of WBC (neutrophils, Lymphocytes, Monocytes, Eosinophils, Basophils)

Gives the percentages of WBC

what does a CBC include:

  • Hemoglobin (Hgb)
  • Hematocrit (Hct)
  • Red blood cell (RBC) count
  • RBC indices
  • White blood cell (WBC) count
  • Platelet count
  • Reticulocyte count (√ bone marrow)
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10
Q

what is hemoglobin ? (Hgb)

A

oxygen carrying protein in RBC

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11
Q

what is hematocrit? (Hct)

A

percentage of RBC in blood

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12
Q

What are RBC indices?

A

MCV – measures RBC volume (macro/normo/microcytic)

MCHC – measures Hgb concentration in single RBC (hypo/hyperchromic)

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13
Q

what is reticulocyte count?

A

assessment of bone marrow function

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14
Q

describe this pictureand the arrows :)

A

to understand abnormal we have to be able to describe normal first

red arrow: center should be 1.3 diameter of whole RBC

Black arow- platlets- not a lot of platlets on blood smears

blue arrow- WBC not a whole lot of WBC on normal blood smears

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15
Q

What is anemic referring to?

What is an H&H?

what is hematocrit?

What are the normal values for Women and Men?

A

Referring to hemoglobin level when they say “I’m anemic”

H&H- hemaglobin and hemoatocrit

Hematorcrit=number of RBC in a sample=H&H

Low hemoglobin=low hematocrit (directly proportional)

If someone has a low hemoglobin level, they are going to have a low hematocrit.

  • Hgb <13.5 g/dL or Hct <41% in men
  • Hgb <12.0 g/dL or Hct <36% in women
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16
Q

why do men have higher values to be reached in their H+H?

A

Muscle mass for men, higher= men need more oxygen to muscles to function so there number is higher

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17
Q

what happens to your hemoglobin when you are bleeding ?

what about acute bleeding ? aka trauma

A

stays normal ….because its just a portion…

In trauma Hemoglobin is normal but you know its not normal because half of the blood has come out and is on the floor in the ER

36-48ish hours later you will see the drop in hemoglobin after acute bleeding and more plasma…H&H will be low

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18
Q

SO what are the 3 things that can cause falsely anemic or normal H+H levels…

A
  • *–Acute bleeding**
  • *–Pregnancy** (“physiologic”=increased blood volume so RBCs diluted but ok! aka dilutional anemia)
  • *–Volume depletion** (hemo-concentrated) “dehydration makes it look like higher [hemoglobin]
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19
Q

how does pregnancy show on an H+H

A

during pregnancy you can increase your blood volume by 50% !!!!!!!! but does not rise the hemoglobin level….they will have more plasma in blood sample…. Appears she has less hemoglobin but she does not

isnt this CRAZY

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20
Q

what about volume depletion how does that affect our H+H

A

let’s say you’re really dehydrated…. You will have less volume in the blood which makes the [hemoglobin] look higher since all of the cells are closer together

Ruth’s Explanation: regarding the dehydration= higher H+H - She misspoke if she said that you will have more plasma if you are dehydrated. If you are dehydrated your blood will have a lower percentage of serum, or plasma, to RBC/WBC/PLT, thus increasing the percentage of your blood that is made up of those cells. Like when you cook down tomatoes to make tomato sauce - as the water cooks off, the sauce gets thicker. It still has the same amount of sugar and fiber etc, they just make up a larger percent of it.

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21
Q

Morphology of RBC

Define:

Microcytic

Macrocytic

Normocytic

give me there MCV numbers and what deficencies you see in each

A

Macrocytic (larger cells)

Microcytic (abnormally small cells)

Microcytic (MCV < 80)
–Iron deficiency
–Thalassemia
–Lead poisoning
Macrocytic (MCV > 100)
–Vitamin B12 deficiency
–Folate deficiency
Normocytic
–Anemia of chronic disease

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22
Q

what does MCV stand for

A

mean corpuscular volume

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23
Q

So what other symptoms do we see with Anemia -low hemaglobin (5)…

and then

what other other signs do we see depending on underlying pathology for anemia? (4)

A

OTher symptoms
•Exertional dyspnea- shortness of breath during exercise
•Dyspnea at rest- SOB
•Palpitations
•Roaring pulsatile (pulsating) sound in the ears
•Rarely, lethargy, confusion, CHF, angina (not getting enough O2), arrhythmia, and/or AMI with severe anemia
Other signs- depends on underlying pathology
•Bounding pulses
•Lymphadenopathy (disease of lymph nodes)
•Hepatosplenomegaly (enlargement to liver and spleen)
•Bone tenderness, especially over the sternum

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24
Q

my sternum is killing me? how come?

A

a lot of bone marrow and RBC are made in sternum…..so could have pain there if anemic

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25
Q

what is the number 1 cause of anemia

A

IRON DEFICIENCY ANEMIA!

GREAT JOB :)

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26
Q

what is it typically cause by in infants?

why is it typically caused by in children?

why is it typically caused by in adults?

it is referring to Iron deficiency Anemia…. sorry :)

A

infants-who love breast milk and have hard time transitioning to food
•Children – typically due to poor diet
•Adults – typically due to blood loss (eg, GI bleed, menses)

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27
Q

signs and symptoms of Iron deficiency Anemia (6)

A

•Signs/Symptoms
–Fatigue
–Cheilitis, glossitis
–Pica and pagophagia (want to eat paint/rocks)
–Koilonychia “spoon nails”

cards on what these wierd words mean later… no worries :)

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28
Q

what Labs for Iron deficieny am i going to order and what am i going to see for results (3 labs tests)

A

•Lab – low serum ferritin <15mcg/L, ↑ TIBC

TIBC= total iron binding capacity

Peripheral blood smear – hypochromic, microcytic (these definitions will come up in a card a little later )
the RBC will look small

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29
Q

hypochromic?

A

RBC look pale due to lack of hemoglobin

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30
Q

microcytic

A

look small and then middle part smaller etc.

think back to the picture of normal blood smar

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31
Q

melena

A

black tarry stool….. yum

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32
Q

hematochezia

A

bright red stool from distal GI bleed

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33
Q

Pica

A

eating non food product

ie. dirt, rocks, and paint!

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34
Q

Pagophagia

A

eating ice!

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35
Q

Koilonychia

A

spooning of nails

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36
Q

what is this?

A

Cheilitis=lesions on corner of mouth

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37
Q

annnd… what is this?

A

Glossitis=smooth sore tongue

Key for “nuitritonal deficient anemia” (B12, folate, and iron)

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38
Q

so if iron deficient anemia happens from my diet then what foods have iron in them?

A

Red meat, pork, poultry, seafood, beans, leafy greens, dried fruit (raisins), iron fortified cereals, breads, pasta

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39
Q

Mother presents wth her 12 month old babe they do labs and find out she has iron deficiency anemia… why is it so common in a 12 month old?

A

weaning from breast milk starts to occur and they can start to get iron deficiency… if they are having a hard time weaning then it can be a problem they just want mom’s milk… they need real food to not get iron deficient .

CBC will show anemia

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40
Q

what are the three things in your work up for someone with iron def. anemia

A
  1. CBC-abnormal
  2. History
  3. Iron level/ iron panel / total iron binging capacity (TIBC)

if you don’t have a lot of iron you will have a lot of TIBC because its waiting to bind to iron.

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41
Q

So we are still talking about nutritional deficiencies if you were wondering….

what are two types of megaloblastic anemias

A

Vitamin B12 & Folate Deficiency

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42
Q

who is at higher risk of devloping Vitamin B12 & Folate Deficiency (4)

A

–Older adults (maybe not getting a good diet)
–Alcoholics (spending money on other things)
–Pure vegans (in animal products)
–Those with malnutrition

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43
Q

how long do i have to have nutirional deficiency to get these anemia’s?

A

–Vitamin B12: takes years
–Folate: takes 4-5 months

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44
Q

WHAT ARE THE TWO STEPS FOR

Vitamin B12 & Folate Deficiency Workup

A

•Step 1 – check vitamin B12 and folate levels… DUH
•If results are borderline or discordant with other clinical features…
•Step 2 – check methylmalonate (MMA) and total homocysteine
–If vitamin B12 deficiency: both elevated
–If folate deficiency: only total homocysteine elevated

MMA AND TOTAL HOMOCYSTEINE WILL ALWAYS LEAD YOU TO THE ANSWER OF EXACTLY WHICH DEFICENCY IT IS!

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45
Q

what do i NEED to rule out when doing a workup of vit B12 and folate defic.? WHY?

A

HAVE TO RULE OUT B12

Have to evaluate for b12 because it can cause irreversible neurologic damage

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46
Q

ALRIGHT…. let’s talk about

Vitamin B12 Deficiency

who do we see it in?

A

Watch for especially in patients with gastric bypass, GI disease (Crohn’s, etc)

again DONT MISS THIS! can cause irreversible neurological damage!

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47
Q

Vitamin B12 Deficiency

SIGNS AND SYMPTOMS (4…well kinda 5)

what are some S/S with late findings (1)

A

–Gait disturbance
–Glossitis
–Anorexia/diarrhea

–Paresthesias (damage to peripheral nerves, pins and needles, tingly), decreased sensory of position (is it up is it down..remember that test?) and vibratory sense

•Late finding – altered mental status
and you know why? because if you miss this it causes IRREVERSIBLE NEUROLOGICAL DAMAGE

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48
Q

Treatment of

Vitamin B12 Deficiency

in PERNICIOUS ANEMIA

A

TX – parenteral B12

FACT: B12 is absorbed in ileum with intrinsic factor, so want to get it parenteral (injection) because if they have pernicious anemia then they don’t have intrinsic factor and can’t absorb it if you take it as a pill. you will have issues…so PARENTERAL IT IS!

(intrinsic factor is too expsensive to give instead of parentral B12!)

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49
Q

What is Pernicious Anemia? and what does it cause?

A

What is it? lack of intrinsic factor

stomach does not make Intrinsic factor in Pernicious anemia

why is this bad aka what does this cause…… so due to a lack of intrinsic factor we get B12 deficiency

so: Pernicious leads to B12 deficency since intrinsic factor absorbs B12

or

B12 Deficency happens BECAUSE you lack intrinsic factor (pernicious anemia)

sorry to say this so many different ways! she just kept stressing this so i wanted to say it as many ways as possible so everyone understands :)

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50
Q

Pernicious Anemia Signs and symptoms (6)

A

–Skin tingling/burning
–Glossitis
–Fatigue, dyspnea
–Leg weakness or spasms
–Imbalance while standing (especially at night)
–Dementia

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51
Q

is Pernicious Anemia associated with other autoimmune disorders?

A

YES!

•Associated with other autoimmune d/o (thyroid & T1DM)

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52
Q

PERNICIOUS ANEMIA

LAB FINDINGS

TREATMENT

A

LABS: antibodies to intrinsic factor (IF)

TX: IM B12

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53
Q

Thalassemia PATHO

A

Impaired production of globin chains (genetic defect)

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54
Q

4 TYPES of Thalassemia? and their symptoms/signs

A

1) Beta minor - asymptomatic
2) alpha minor – asymptomatic

3) Beta Major- (present ~6 months old) –
–Pallor
–Growth retardation
–Hepatosplenomegaly(HSM), jaundice
–Abnormal skeletal development, “chipmunk” facies
4) Alpha major – incompatible with extra-uterine life

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55
Q

Beta Thalassemia Major (BTM)

what ar the characteristics on the blood smear? what specific cell do you see characteristic of this?

treatment for BTM?

name two types in thalassemia that require different treatments?

A
  • BTM – profound (KEY!) hypochromic, microcytic anemia with bizarre RBC morphology (“Target cells”)
  • BTM TX – life-long transfusions

2 types: heterozygote’s (minor)– much more mild symptoms

homozygote’s (major) – life-long transfusions (BTM)

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56
Q

what type of anemia is Thalassemia?

A

INHERITED ANEMIA (not nutritional)

People may have minors (remember the four types there were two types of minors that were asymptomatic) and never know it

Around 6 months the infant now produces its own hemoglobin but there is a defect and it now causes a defect in the child.

again blood smear apperance : Hypochromic, microytic, profoundly low

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57
Q

Tell me about the apperance and symptoms that happen in a child with Beta Thalassemia Major?

A

Child will fall off the growth cord!

Facial and skull features will be deformed

hoffman described this as a: Chipmunk face

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58
Q

what is unique in the Beta Thalassemia Major peripheral blood smear?

A

It will have target cells!

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59
Q

what will children with Beta Thalassemia Major need for life?

A

Will need life long transfusions

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60
Q

What is sickle cell anemia?

A

HEMOLYTIC ANEMIA

•Production of abnormally-shaped RBCs
–Subtype causing anemia: homozygous hemoglobin S
•Diminished ability to function as RBCs
–Vasoocclusion
–Hemolysis

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61
Q

Signs and Symp. of Sickle Cell Anemia (4)

A

–Dactylitis (acute pain in the hands and/or feet) [the vessels more easily occulde causing issues]
–Joint pain
–Splenic sequestration
–Multiorgan/multisystem dysfunction or failure

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62
Q

what age does sickle cell show up at?

A

AGE 2

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63
Q

tell me all about this picture and whats the problem with it?

A

Crescent or “Sickle” shaped

They look sharp…. They get stuck in blood stream— spleen gets big because its trying to clean up the messed up RBC

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64
Q

painful episode? what is that? how long can it last?

A

Previously referred to as SICKLE CELL CRISIS

•No identifiable cause; lasts 2-7 days
•Can affect any area of the body….. it is basal occulding
•Pain trivial to excruciating
•½ of episodes accompanied by:
–Fever
–Swelling
–Tenderness
–Tachypnea
–Hypertension
–Nausea/vomiting

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65
Q

What do you not want to miss with SICKLE CELL ANEMIA

A

Acute Chest Syndrome (ACS)

this should be at the TOP of your differential with Sickle Cell Disease (SCD)

66
Q

what is Acute Chest Syndrome (ACS)

definition?

A

•Leading cause of death in patients with SCD
•Defined as:
–New radiodensity (consolidation) on chest x-ray PLUS fever and/or respiratory symptoms
•Unclear etiology

67
Q

Acute Chest Syndrome (ACS)

signs/symptoms

A

–Temperature ≥38.5°C
–Tachypnea
–Intercostal retractions, nasal flaring, or use of accessory muscles
–Chest pain
–Cough, wheezing, rales

*******Always look for it; progresses rapidly

68
Q

Acute Chest Syndrome (ACS)

treatment

A

•TX – broad spectrum abx & ICU admission

69
Q

what is going on here?

A

Acute Chest Syndrome

Left side- radioopaque…. Probably fluid collection

70
Q

Glucose 6-phosphate dehydrogenase (G6PD) Deficiency

what is it?

as if we have not heard about this deficiency enough!

A

Anemia caused by enzymatic disorder of RBC

  • Most common enzymatic disorder of RBCs in the world (up to 400 million people)
  • G6PD protects RBCs against oxidant injury; deficiency results in hemolysis

Kids born with it

They don’t have enzyme at all

Newborns when born are screened for this

71
Q

Glucose 6-phosphate dehydrogenase (G6PD) Deficiency

signs and symptoms

A

–Asymptomatic
–Jaundice (neonatal, hyperbilirubinemia)
–Pallor, dark urine ± abdominal/back pain

72
Q

Can you have G6PD and not know as an adult?

A

sure thing!

Adult may present with this with no history of diagnosis because they are fine and have mild disorder (enzyme but not a lot of it) but then they can get a fava bean and then come to your office and BAM THEY HAVE IT

73
Q

Triggers of G6PD Deficiency

A

Triggers:

  • infection
  • drugs (eg, nitrofurantoin)
  • chemicals (eg, methylene blue, dyes)
  • fava beans
74
Q

how does a blood smear look with G6PD Deficiency

what is the important cells only seen in this disease?

A

•Peripheral blood smear:
–Heinz bodies
–Bite cells

75
Q

Screening tests for G6PD deficiency?

A

–Fluorescent spot test

76
Q

Treatment for G6PD Deficiency

A

mild form: avoid triggers

severe form: transfusion

77
Q

What is Aplastic Anemia

and what do you have to get?

A

basically LOW EVERYTHING

•Pancytopenia= deficiency of all three cellular components of the blood (red cells, white cells, and platelets)

  • Neutropenia (↓ WBCs)
  • Thrombocytopenia (↓ platelets)
  • Anemia (↓RBCs)
  • Decreased # reticulocytes

you get a bone marrow biopsy…

78
Q

what are the two types of aplastic anemia

A

–Inherited congenital bone-failure syndromes
•eg, “Fanconi’s”
–Idiopathic, acquired (much more common)

79
Q

what are potential causes of aquired aplasic anemia (4)

A

•Potential causes of acquired:
–Viral infection
–Drugs
–Toxic chemicals
–Autoimmune

80
Q

Inherited Bone-Failure Syndromes (Fanconi’s)

signs and symptoms

A

–Abnormal skin pigmentation
–Short stature
–Renal, cardiac, GI abnormalities
–Microcephaly
–Hypogonadism
–Skeletal anomalies

81
Q

Acquired Aplastic Anemia signs and symptoms (7)

A

•Signs/symptoms (insidious onset):
–Pallor
–Petechiae (pinpoint dots on the skin from micro-hemmoraging)
–Purpura
–Ecchymosis
–Mucosal and gingival bleeding
–Vaginal bleeding
–Active bacterial infections

Fine up until trigger that causes bone marrow to stop producing those cells

82
Q

Whats wrong with having decreased platelets, WBC, RBC in Aplastic Anemia?

A

No platelets-Can’t clot=Bruising = bleed more

NO WBC- get sick

No RBC- O2 carrying capacity out the window

83
Q

Difference between Ecchymosis/purpura/petechiae

A

= all bleeding into skin… not much difference

84
Q

Differene between Petechiae and rash

A

Determine if there is blanching or not.

Petechiae will not blanch. This is because petechiae is caused from blood vessels breaking under the skin, therefore with applied presure to the area, it will stay red.

However, a rash will blanch. This is because rashes involve blood vessels that have remained intact. When you apply pressure to the rash, you are occluding the blood vessels in the dermis, therefore the skin will turn white (blanch). When you release the pressure, the skin will return back to red because you are releasing pressure off of the blood vessels.

85
Q

Petechiae

what is it? what is it caused by?

A

little pinpoint dots on the skin that come from microhemmoraging

caused by decreased platelets, thrombocytopenia

86
Q

whats this?

A

petechiae

87
Q

what this?

A

purpura

they are bigger!

88
Q

what’s this?

A

ecchymosis

biggest

89
Q

what is Anemia of Chronic Disease

and its PATHO?

A
  • Associated with infectious, inflammatory or neoplastic disease (eg, CKD, RA, leukemia)
  • Typically normochromic, normocytic, hypoproliferative, and mild in degree

Pathogenesis:
–reduction in red blood cell (RBC) production by bone marrow
–mild shortening of RBC survival
–Inability to ↑ erythropoiesis in response to anemia

*******Side comment Hoffman said: ****************

RBC look normal but there are not. Does not happen acutely it is after several years of having a chronic disease.

90
Q

Signs and Symptoms of Lead Poisoning

A

Has vague symptoms:

–“Lead colic” abdominal pain
–Anemia
–Headache, irritability
–Confusion

91
Q

Where do you get the most lead exposure?

A

most due to lead exposure at work (ie. glass industry, auto industry)

92
Q

SO, I’m a new provider what happens if I miss lead poisoning?

A

•If you miss it – irreversible damage (nervous system, kidneys & other organ systems)

GREAT! SO DON’T MISS IT! :D

93
Q

HOW DO YOU DIAGNOSIS LEAD POISONIG?

(by lab value)

A

•DX – blood lead level >80 mcg/dL

94
Q

AHHH, WHAT IS WRONG WITH ME?

A

lead collects on the gum line… so check it out!

95
Q

what is so unique to the lead poisoning blood smear? if you see this word you 100% KNOW ITS LEAD POSIONING?

A

BASOPHILIC STIPPLING ON PERIPHERAL BLOOD SMEAR! = LEAD POISONING

96
Q

HOW DO YOU TREAT LEAD POISONING

A

chelation

97
Q

I KNOW IT’S A LOT!

BUT GUESS WHAT!

A

WE ARE DONE WITH ANEMIA!

now onto Disorders of the RBC’s

98
Q

what is Polycythemia Vera

what are the levels for hemoglobin that indicates this?

A

•Myeloproliferative disorder=Disorder of RBC-makes a ton of RBC’s
•Often found incidentally on CBC
–Hemoglobin >18.5 in men or >16.5 in women
–Persistent leukocytosis (elevate WBC) & thrombocytosis (Elevated Platelets) because bone marrow over producing

99
Q

signs and symptoms of Polycythemia Vera (5)

A

–Splenomegaly
–Headache
–Generalized pruritus (post-bath)-severe ithching
–Unusual thrombosis (clotting)
–Erythromelalgia (hands turn colors)

100
Q

How do we treat Polycythemia Vera

A

PHLEBOTOMY to remove excess RBC

only makes sense … :D

101
Q

Erythromelalgia

A

hands change colors

normal pulse but change in color of hands

**specific to polycynthemia vera**

102
Q

Coagulopathies (3 things she mentioned)

A

Coagulopathies: “Royal disease” (cause a queen had it or something ) (also called clotting disorder and bleeding disorder) is a condition in which the blood’s ability to clot (coagulate) is impaired. This condition can cause prolonged or excessive bleeding, which may occur spontaneously or following an injury or medical and dental procedures.

  1. Hemophilia- A disorder in which blood doesn’t clot normally.
  2. Hypercoaguable State: the blood shouldn’t clot when it’s just moving through the body. If blood tends to clot too much, it is referred to as a hypercoagulable state or thrombophilia.
  3. Hypocoaguable State: so just the other way around… you don’t clot.
103
Q

What is the most inheritied hypercoagulability disorder in Caucasian’s

A

Factor V Leiden

104
Q

What is a risk with Factor V Leiden?

how do people with this usually present?

A

•Risk of venous thromboembolism (DVT or PE) although most asymptomatic

A lot of time they present with a clot

105
Q

What do you ALWAYS ASK ABOUT BECAUSE OF Factor V Leiden

A

•Ask about hx clotting (PMH & FH)

Blood clots in family members? During history

******Before going on Birth control- ASK! because estrogen in BC causes blood clots

So then put on progesterone instead

NEVER BE ON ESTROGEN with history of blood clots.

106
Q

Treatment of Factor V Leiden

A

TX

  • anticoagulation if clot,
  • ↓ clotting risk through lifestyle
  • modify risk
107
Q

What is Immune Thrombocytopenia

A

Former term: idiopathic thrombocytopenia purpura (ITP)

•Acquired, thrombocytopenia caused by autoantibodies against platelet antigens

Thrombocytopenia: deficiency of platelets in the blood. This causes bleeding into the tissues, bruising, and slow blood clotting after injury.

108
Q

How do patients present with Immune Thrombocytopenia

aka what do you see on your exam?

A

petechiae, purpura, epistaxis

show up complaining of bleeding

109
Q

What is this?

A

purpura

110
Q

Triggers of Immune Thrombocytopenia

A

viral infection & systemic conditions (eg, SLE) that disrupt immune homeostasis

111
Q

Treatment of Immune Thrombocytopenia

A

glucocorticoids unless actively bleeding than IVIG (IV immunoglobulin)

112
Q

What is Hemophilia?

what are the two types?

A
  • X-linked recessive disorder
  • A – Factor VIII deficiency; B – Factor IX deficiency

Bleed into the joints —2 year old with huge knee…

Joint destruction from so much bleeding

113
Q

signs and symptoms of Hemophilia

Late complications?

A

–Easy bruising
–Hemarthrosis (80% of hemorrhage occurs in joints)

•Late complications – ICH (intracranial hemorrhage), joint destruction

114
Q

at what age is this usually presented and why? (hemophilia)

A

Usually present @ 1-1.5 years old

Kids around 1 year of age –start walking and start falling

parents bring them in because OMG MY KID WON’T STOP BLEEDING

115
Q

WHAT LAB DO YOU GET FOR HEMOPHILIA

A

prolonged PTT: partial thromboplastin time

116
Q

What is the treatment of Hemophilia

A

factor VIII for hemophilia A

factor IX for hemophilia B

117
Q

Is hemophilia rare?

A

yes more likely child abuse (which is so sad)

Prof. Hoffman said always air on the side of caution and do a child abuse workup to make sure its not that :(

She gave the example of a head contusion she said that is more likely child abuse then hemophilia.

118
Q

what are spontaneous hemarthrosis

A

large joints in hemophilia

119
Q

What is von Willebrand Disease

A
  • Most common inherited bleeding d/o
  • Platelets have normal morphology but lack factor VIII/vWF complex – impacts ability to adhere
120
Q

What are the three types of von Willebrand Disease

A

•3 types:

  1. mild to moderate decrease vWF
  2. dysfunction of vWF
  3. absolute lack of vWF
121
Q

what is the most common hypocoagulative disorder?

A

von Willebrand Disease

122
Q

TO see if someone is Hypocoagulative what kinds of questions can you ask?

A

When you go to the dentist to you bleed A TON?

After surgery do you need blood transfusion?

Heavy heavy menstrual cycle?

123
Q

signs and symptoms of von Willebrand Disease

A

–Easy bruising w/ hematoma
–Skin bleeding
–Prolonged bleeding from mucosal surfaces (eg, epistaxis, dental/sugery, GI, menorrhagia)

124
Q

how do you diagnosis von Willebrand Disease

A

increased bleeding time, normal platelet count

Platelets are normal they just can’t adhere

Bleeding time will see how well they can adhere

125
Q

What is the treatment of von Willebrand Disease

A

•TX of mild mucosal bleeding with DDAVP – desmopressin –it acts by increasing circulating levels of factor VIII and vWF

126
Q

Alright guys almost there…. lets start Oncology

A

and just remember this is the only lecture for CA for the exam so by doing these flashcards you are almost done with studying for CA

:)

127
Q

what is Multiple Myeloma

A
  • Classic – older patients with atraumatic back pain
  • Plasma cells proliferate in bone marrow causing destruction of skeleton “punched out lesions”

Cancer of bone marrow!

128
Q

What are signs and symptoms of Multiple Myeloma (4)

A

–Bone pain “punched out lesions”
–Fatigue/generalized weakness

-decreased reflexes
–Weight loss

129
Q

What do x-rays look like in Multiple Myeloma

A

•X-ray shows “punched out” lesions

Get an x ray

Plasma cells are proliferating in bone and causes this punched out thing on x-ray

Then bone scan to see where lesions are

Raadiolucent air where the holes are

130
Q

What will Multiple myeloma x ray show

A

punched out

131
Q

What labs do you do for multiple myeloma

A

hypercalcemia, renal insufficiency, anemia

132
Q

What does the exam reveal for multiple myeloma?

what are some Ddx that you should be thinking of?

A

•Exam – decreased reflexes

Ddx- osteoarthritis, vertebral compression factor, herniated disc

133
Q

What is going to be your diagnostic workup for multiple myeloma?

A

•Diagnostic workup: bone marrow biopsy

In the hip…. Posterior superior iliac crest

134
Q

Multiple Myeloma blood smear

A

see a lot of B cells

135
Q

What are the 4 types of Leukemia and differntiate acute from chronic?

A

Leukemia=blood cancer

90%of all leukemia’s are in adults!

If it is child Leukemia then most common is acute

  1. Acute lymphoblastic leukemia (ALL)- rapid development of immature cells (mostly blast cells) most common in kids
  2. Chronic lymphocytic leukemia (CLL)
  3. Acute myeloid leukemia (AML)
  4. Chronic myeloid leukemia (CML)

•Acute – rapid ↑immature WBCs (aka “blast” cells)
Chronic – excessive buildup of mature but still abnormal WBCs

136
Q

Casue

and

risk factors of leukemia (6)?

A

•Exact cause of leukemia is unknown

•Risk factors:
–Smoking
–Ionizing radiation
–Chemicals (eg, benzene)
–Prior chemotherapy
–Down syndrome
–Family history of leukemia

137
Q

symptoms of leukemia

(hint: it’s a whole diagram of symptoms)

A

NONSPECIFIC

comes into your office is “Soooo run down, extremely tired, can’t get rid of the cough”

you say alright lets give it another week or two

Symptoms failed to resolve and he went back

Extremely high WBC count—he had leukemia

Hoffman told us this story… who knows if she’ll take questions from experiences she’s had. so here it is :)

138
Q

LeuKemia Cutis

A

Rash primarily on face and chest

139
Q

what is this?

A

splenomegaly in leukemia

140
Q

Leukemia Diagnostic Studies

A
  • CBC with differential
    • Leukocytosis (↑WBCs) – hallmark (crowds out other cells which is why you se decrease in other stuff)
    • Anemia (↓H+H)
    • Thrombocytopenia
  • Peripheral blood smear & bone marrow biopsy abnormalities
  • Gene testing (do this with a chronic type)
    • Philadelphia chromosome in CML
141
Q

What is the hallmark in Leukemia?

A

high WBC count

And then low everything else because WBC hogging all the space

142
Q

Leukemia treatment

A

TX (depends on type & age of the person)
–Usually combination of:
•Chemotherapy
•Radiation
•Bone marrow transplant
•and/or Watchful waiting

older age - watch and wait

143
Q

Signs and symptoms of Lymphoma (5)

A
  1. Painless lymphadenopathy
  2. “B” symptoms (if present, aggressive lymphoma) these things happen EVERY NIGHT!
    • Fever >38ºC (>100.4ºF)
    • Weight loss >10% over the past 6 months
    • Night sweats (drenching)
  3. Pruritis (generalized itching)
  4. Anorexia
  5. SOB if nodes become restrictive
144
Q

How does patint present with lymphoma?

A

Non tender palpable lymph node

145
Q

Descirbe X-ray findings for lymphoma

A

Could pick it up on chest x-ray and having a large mediastinal mass

146
Q

Hodgkin’s vs Non-Hodgkin’s

explain key difference between the two?

A
  • If Reed-Sternberg cell present -Hodgkin’s
  • If Reed-Sternberg cell not present - NHL
  • DX – lymph node biopsy
147
Q

What does the Reed Sternberg cell look like on a blood smear

A

OWL’S EYES

148
Q

Most common malignancy of head and neck in children (teenagers mostly)

A

Hodgkin’s Lymphoma

149
Q

Hodgkin’s Lymphoma

age of onset?

Exam findings?

A
  • Ages: 15-35 and >55
  • Exam – nontender, firm, rubbery consistency cervical and/or supraclavicular node(s) neck and above!!! KEY!; mediastinal mass on routine chest x-ray
150
Q

Non-Hodgkin’s Lymphoma

what is it?

exam findings?

A
  • Most common type – 60,000/yr in U.S.
  • Group of 20+ types
    • eg, Burkitt lymphoma – fastest growing tumor, most common in abdomen
  • EXAM Findings: Lymphadenopathy below the clavicles, multiple peripheral nodes
  • Can die within days because tumor is so fast growing

Doubles every 24 hours

151
Q

what is Neutropenic Fever

A

oncology emergency

•Cancer patients receiving chemotherapy – at risk for invasive infection due to colonizing bacteria and/or fungi that translocate across GI mucosal surfaces

152
Q

what could be your only sign for Neutropenic Fever

A

•Fever may be earliest & only sign of infection

EMERGENCY!

153
Q

What do you have to do early with Neutropenic Fever and what do you do to treat it?

A

•Recognize early; initiate broad-spectrum antibx to avoid sepsis & possibly death

If present with fever this has to be TOP OF LIST.

IV ABX need to be given 60 min from presentation!

154
Q

What is neutorpenia related to neurtopenic Fever

A

•Neutropenia defined as absolute neutrophil count <500 cells/microL

155
Q

okay great, so now we know what neutropenia…. what does Absolute Neutrophil Count mean?

A

ANC = total white blood cell (WBC) count x percentage of polymorphonuclear cells (PMNs) and bands

156
Q

Is Neutopenic Fever an emergency?

what must the fever be?

A
  • Fever >38.3°C (101°F)
  • Oncologic emergency!
157
Q

NICE JOB GUYS!

hope these helped!

only thing not on here is that little paper packet she gave us with normal lab values on it that we have to know..

I may add those in later this weekend :)

other then that… enjoy and happy studying!

A
158
Q

how many more times is the hematocrit than the hemoglobin? (usually)

A

3x more!

159
Q

what is the fastest growing tumor and where is it found?

A

burkitts lymphoma, in abdomen

doubles in size every 24 hours and pt can die within days

160
Q

what does the term left shift mean

A

increase in release of immature cells, sometimes called “stabs” indicating inflammatory response