Beruflich Dokumente
Kultur Dokumente
Khristy C
Tjiang kelvin
Steven matuali
07120100107
07120110030
07120110055
ETIOLOGI OF ANEMIA
1. BLOOD LOSS / Erythrocyte loss
a. Acute : HEMORRHAGE
b. Chronic : LOW-VOLUME LOSS
2.EXCESSIVE BLOOD CELL DESTRUCTION /HEMOLYSIS
a.Hereditary abnormalities : erythrocyte membrane,
hemoglobinopathy
b.Aquired abnormalities : immunologic defect, obstetric infection, chemistry,
physic, mechanic abnormality.
3.DEFICIENT RED BLOOD CELL PRODUCTION
(ineffective hematopoiesis).
a. Nutritrional anemia : protein, folic acid, Fe, vit B12 def
b. Bone marrow failure : aplastic anemia, anemia in malignancy
c. low erythropoietin or Decreased marrow response to erythropoietin
Anemias may be classified morphologically based on the average size of the cells and
the hemoglobin concentration into:
Macrocytic
Normochromic, normocytic
Hypochromic, microcytic
CLINICAL EVALUATION :
The causes anemia suggested from history and physical examination :
HISTORY
- blood loss : obvious and dramatic clue to the causes anemia.
- History of anemia reaches back to childhood is highly suggestive of a
hereditary disorder ---especially congenital hemolytic anemia.
- sudden onset pancytopenia in healthy individual may be explain with
history of exposure to toxic chemicals or new medication.
-TRANFUSION HISTORY
- PAST BLOOD COUNT MEASUREMENTS
-NUTRITIONAL HABIT
-ACUTE OR CHRONIC ILLNES : WEIGHT LOSS, FEVER, NIGHT
SWEATS .
SYMPTOMS: weakness or fatigue in general or during exercise, malaise
and poor concentration , headache, dizziness .
Severe anemia -dyspnoe (shortness of breath) on exertion.
PHYSICAL EXAMINATION :
PHYSICAL SIGN DEPEND ACUTE OR CHRONIC OF ONSET :
ACUTE BLOOD LOSS SHOW SIGNS HYPOXIA AND HYPOVOLEMIA
(FOR EXAMPLE TACHYCARDIA AND HYPOTENSI ORTHOSTATIC ) --LOSS 40 % BLOOD WILL EXHIBIT IN SIGN AND SYMTOMPS
HYPOVOLEMIC SHOCK
ANEMIA DEVELOPS GRADUALLY BODY HAS TIME TO INCREASE
PLASMA VOLUME :
--- IN YOUNGER INDIVIDUAL SIGNS AND SYMTOMS NOT
APPEAR UNTIL Hb 7 8 g/dL
--- IN OLDER : Hb 10 g/dL CAN BE SYMTOMPMATIC
(EXSPECIALLY PATIENT CVD OR ATHEROSCLEROTIC).
GENERAL : SKIN AND MUCOUS MEMBRANE PALLOR
( LESS REALIBLE INHEAVILY PIGMENTED PATIENTS)
Macrocytic Anemia
Etiologi
1.Megaloblastic anemia, the most common cause of macrocytic anemia
(due to a deficiency of either vitamin B12, folic acid (or both).
Deficiency in folate and/or vitamin B12 (inadequate intake or insufficient
absorption)
Folate deficiency normally does not produce neurological symptoms, while
B12 deficiency does.
2.Pernicious anemia is an autoimmune condition-- decrease intrinsic factor
produced by the parietal cells of the stomach. Intrinsic factor is required to
absorb vitamin B12 from food-- destruction of intrinsic factor --- poor absorption
of vitamin B12.
3. Removal of the functional portion of the stomach--- during gastric bypass
surgery, leading to reduced vit B12/folate absorption.
4. Hypothyroidism
5. Alcoholism , liver Disease coomonly causes a macrocytosis, although not
specifically anemia.
6 Methotrexate, zidovudine, and other drugs that inhibit DNA replication.
Folate Deficiency
MCV
> 100
> 100
Smear
Macrocytosis with
hypersegmented
neutrophils
Macrocytosis with
hypersegmented
neutrophils
Pernicious anemia
Yes
NO
Homocystine
Elevated
Elevated
Methylmalonic Acid
Elevated
NORMAL
NORMOCYTIC ANEMIA
Normocytic anaemia occurs when the overall hemoglobin
levels decreased, but the red blood cell size (MCV)
remains normal.
Causes :
Acute blood loss
Anemia of chronic disease
Aplastic anemia (bone marrow failure)
Hemolytic anemia
HEINZ BODY ANEMIA
Heinz Bodies are an abnormality that form on the cells in
this condition.
This form of anemia may be brought on by taking certain
medications; acetaminophen (Tylenol).
MICROCYTIC ANEMIA
Microcytic anemia is primarily a result of hemoglobin synthesis failure/insufficiency,
Etiologies:
1.HEME SYNTHESIS DEFECT
Iron deficiency anemia
Anemia of chronic disease (more commonly presenting as normocytic anemia)
2.GLOBIN SYNTHESIS DEFECT
alpha-, and beta-thalassemia
HbE syndrome
HbC syndrome
3.SIDEROBLASTIC DEFECT
Hereditary sideroblastic anemia
Acquired sideroblastic anemia, including lead toxicity
Reversible sideroblastic anemia
Iron-Deficiency Anemia
An iron deficiency inhibits Hb synthesis, leading to hypochromic microcytic
anemia: MCH "26 pg, MCV "70 fL, Hb "11 g/L.
The primary causes are:
blood loss (most common cause); 0.5mg Fe are lost with each mL of blood;
insufficient iron intake or absorption;
increased iron requirement due to growth, pregnancy, breast-feeding, etc.;
decreased iron recycling (due to chronic infection);
Iron-Deficiency Anemia
Clinical Manifestations
Most common: pallor
Second most common: inflammation of the tongue
(glossistis)
Cheilitis=inflammation/fissures of lips
Sensitivity to cold
Weakness and fatigue
Diagnostic Studies
CBC
Iron studies Diagnostics:
Iron levels: Total iron-binding capacity (TIBC), Serum Ferritin.
Endoscopy/Colonscopy
Sources
of
Physical Manifestation :
Spoon Nails in Iron
Deficiency
iron
to
make
hemoglobin
1.iron
supplement
2.
meat
red meat, such as beef or liveras well as chicken, pork, fish, and shellfish.
3.Nonmeat
foods
sources
of
iron
include:
Spinach
and
other
dark
green
leafy
vegetables
Peanuts, peanut butter, and almonds , Eggs ,Peas; lentils; and white, red, and
baked
beans
Measurements of Anemia
Red cell distribution width (RDW) is a measurement of the variation
in RBC cell size
Standard deviation/mean MCV x 100
The range for normal values is 11.5-14.5%
A value > 14.5 means that there is increased variation in cell size
above the normal amount (anisocytosis)
A value < 11.5 means that the RBC population is more uniform in
size than normal.
Treatment anemia
Goals of Treatment
1.to increase the red blood cell count and/or
hemoglobin level.
2.to treat the underlying condition or cause of the
anemia.
3.
severe
of
these
medicines
include:
*Antibiotics
to
treat
infections.
*Hormones to treat adult and teenaged women who have heavy
menstrual
bleeding.
*erythropoietin to stimulate body to make more red blood
cells.
*Chelation
therapy
for
lead
poisoning.
anemia
medical
procedure
1.blood
2.blood and marrow stem cells transplants.
Procedures
to
treat
it
transfusions
Diagnostic Studies
Mucosal cell
Aplastic Anemia
19/04/2011
Clinical Manifestations
Gradual development
Symptoms caused by suppression of any or all bone marrow
elements
General manifestations of anemia
Fatigue
Dyspnea
Pale skin
Frequent or prolonged infections
Unexplained or easy bruising
Nosebleed and bleeding gums
Prolonged bleeding from cuts
Dizziness
headache
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