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Overview. Classifications of anemiaInvestigative toolsBlood smear componentscase studiesiron deficiency anemialead poisoning. Classification of Anemia. Blood lossImpaired red cell formationHemolytic anemia. Classification of Anemia. Impaired red cell formationdeficiencybone marrow failuredyshematopoietic anemia.
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1. ANEMIA IN CHILDHOOD Presented by
Ruth Anne Herring, RN, MSN, CPNP
Pediatric Nurse Practitioner
Texas Children’s Cancer Center
2. Overview Classifications of anemia
Investigative tools
Blood smear components
case studies
iron deficiency anemia
lead poisoning
3. Classification of Anemia
Blood loss
Impaired red cell formation
Hemolytic anemia
4. Classification of Anemia
Impaired red cell formation
deficiency
bone marrow failure
dyshematopoietic anemia
5. Classification of Anemia
Hemolytic Anemia
corpuscular
membrane defects
enzyme defects
hemoglobin defects
extracorpuscular
immune
isoimmune
autoimmune
idiopathic
6. Approach to Diagnosis of Anemia detailed history
careful physical examination
peripheral blood smear
red cell morphology
MCV
RDW
WBC and platelet morphology
bone marrow evaluation
additional testing
7. History
diet
family history
environmental exposures
symptoms (headache, exertion dyspnea, fatigue, dizziness, weakness, mood or sleep disturbances, tinnitis)
8. Physical Examination pallor
jaundice
tachycardia
tachypnea
orthostatic hypotension
venous hum
systolic ejection murmur
t peripheral edema
splenomegaly
glossitis
gingival pigmentation
9. Peripheral Blood Components RBC
Hgb
HCT
MCV - a calculated value
MCH
RDW
Reticulocyte Count
10. Red Cell Morphology
anisocytosis
poikilocytosis
elliptocytes
Howell-Jolly bodies
Cabot’s rings
Heinz bodies
Sickled cells
Spiculated/Crenulated red cells
Target cells
Basophilic stippling
11. Using MCV to Characterize Anemia
Hypochromic Microcytic
Iron deficiency anemia
Thalassemia
Sideroblastic anemia
Chronic infection
Lead poisoning
Hemoglobin E trait
Inborn errors of iron metabolism
Copper deficiency
Severe Malnutrition
12. Using MCV to Characterize Anemia
Macrocytic
Normal newborn
Increased erythropoiesis
Post-splenectomy
Liver disease
Obstructive jaundice
Aplastic anemia
Hypothyroidism
Megaloblastic anemia
Down’s syndrome
13. Using MCV to Characterize Anemia Normocytic
Acute blood loss
Infection
Renal failure
Connective tissue disorder
Liver disease
Disseminated malignancy
Early iron deficiency
Aplastic anemia
Bone marrow infiltration
Dyserythropoietic anemia
14. Using MCV and RDW
15. Using MCV and RDW
16. Differential diagnosis of microcytosis
17. Iron Deficiency Anemia causes
Dietary deficiency
Increased demand (growth)
Impaired absorption
Blood loss
gut problems
gall bladder
lung
nose
heart
kidney
menstrual problems
trauma
18. Iron Deficiency Anemia Symptoms
GI
anorexia
pica
atrophic glossitis
guaiac positive stool
CNS
fatigue
irritability
Cardiac
increased cardiac output
cardiac hypertrophy
Musculoskeletal
impaired exercise performance
radiographic changes
19. Iron Deficiency Anemia
characteristics of peripheral blood smear
microcytic
hypochromic
20. Iron Deficiency Anemia
additional diagnostic tests
free erythrocyte protoporphyrin (elevated)
serum ferritin (decreased)
serum iron (decreased)
Iron binding capacity (increased)
Iron saturation (decreased)
21. Iron Deficiency Anemia Treatment
oral iron supplementation: 6mg/kg/day of elemental iron
for at least 3 months
check retic count after 2 weeks
side effects (educate family)
goal: to replace iron stores, not just circulating Hgb
22. Iron Deficiency Anemia failure to respond to therapy
non-compliance
inadequate dose
ineffective preparation
unrecognized blood loss
impaired GI absorption
coexistence of disease
incorrect diagnosis
23. Iron Deficiency Anemia
parenteral therapy
indications
poor compliance
severe bowel disease
intolerance of oral iron
chronic hemorrhage
acute diarrhea disorder
24. Dosing of Parenteral Therapies Iron Dextran
provides 50mg/ml elemental iron
for weight >15kg: dose (ml) =
0.0442 (desired Hgb - Observed Hgb) x LBW + (0.26 x LBW)
LBW (males)=50kg+2.3kg/inch of height over 5 ft.
LBW (females )=45.5kg+2.3kg/inch of height over 5 ft.
For weight 5 - 15kg: dose (ml) =
0.0442 (desired Hgb - Observed Hgb) x W + (0.26 x W)
W = wt in kg
25. Dosing of Parenteral Therapies
Ferrlecit (sodium ferrous gluconate)
each 10cc provides 125mg elemental iron
dilute 10ml in 100ml 0.9NS and administer IV over 1 hour
repeat for up to 8 sessions
test dose recommended
26. Anemia of Lead Poisoning epidemiology
air
water
food
soil
paint
folk remedies
miscellaneous (cosmetics, pottery, live near lead industry) Risk factors
age
nutrition
pica
developmental delay
27. Anemia of Lead Poisoning symptoms
NONE!
With levels >60 mcg/dl
lead colic
constipation
anaorexia
hyperirritability
anemia
28. Anemia of Lead Poisoning fetus and infant more vulnerable to damaging effects
more susceptible with concurrent iron deficiency anemia
effects of prolonged exposure to mild elevations
neurologic deficits
decreased in IQ (2-3 points for every 10mcg/dl of lead)
speech and language delays
hearing loss
29. Anemia of Lead Poisoning
characteristics of smear
hypochromic
normocytic or microcytic
sideroblasts
basophilic stippling
30. Anemia of Lead Poisoning
diagnostic tests
blood lead level
X-rays of long bones
31. Anemia of Lead Poisoning prevention is the cure!
Primary prevention:
removal of lead from gasoline
removal of lead from paint
Secondary prevention
edcuation
soil abatement
dust abatement
pain hazard remediation (18-23% decline in lead levels >25mcg/dl)
32. Anemia of Lead Poisoning treatment - chelation
Chelation: decreases blood lead levels, does not decrease lead already in tissues
<10 mcg/dl: non-toxic
10-14 mcg/dl: low lead level exposure
parental education
15-19 mcg/dl: mild lead poisoning
risk of neurodevelopmental effects
parental education for lead exposure reduction
33. Anemia of Lead Poisoning
treatment
> 20 mcg/dl: medical evaluation and identification of environmental sources
20-44 mcg/dl: lead hazard control, involvement of Case Mgr or Social Worker
consider oral chelation if levels persist after environmental intervention
34. Anemia of Lead Poisoning 45-69 mcg/dl
Abdominal X-ray for enteral lead deposits
DMSA (for children without encephalopathy)
30mg/kg/day divided TID x 5 days followed by 20mg/kg/day divided BID x 2 weeks
may repeat course every 2 weeks
or CaNa2EDTA (requires hospitalization)
25mg/kg/day x 5 days by continuous infusion or in divided doses
repeat if lead level >45mcg/dl within 7-14 days of tx
35. Anemia of Lead Poisoning 70-90 mcg/dl
MEDICAL EMERGENCY requiring immediate hospitalization
monitor for increased ICP
monitor hemodynamic stability
osmotic therapy and drug therapy
chelation therapy
BAL and CaNa2EDTA combination therapy
Initiate therapy with BAL only
25mg/kg/day in 6 divided doses by IM injection
4 hours after initial BAL injection, begin CaNa2EDTA
50mg/kg/day either as continuous IV infusion or divided doses IV over 4-6 hours
IM injections are simpler but more painful
36. Anemia of Lead Poisoning 5-7 days after initial tx with BAL / CaNa2EDTA
if lead level is 45-69mcg/dl
give second course of CaNa2EDTA
if lead level is >70mcg/dl
repeat course of BAL / CaNa2EDTA
48 hours after second course, if lead level remains 45-69mcg/dl
7 days after second course, begin course of CaNa2EDTA
37. Lead Chelation BAL
chelates lead in the brain
given IM
side effects: febrile reactions, elevated liver enzymes, N/V, headache, conjunctivitis, rhinorrhea, lacrimation, salivation
contraindicated for persons with
peanut allergy
G6PD deficiency
38. Lead Chelation CaNa2EDTA
only agent proven to improve IQ scores
usually given as slow IV infusion; rapid IV infusion may case encephalopathy
IM painful if not mixed with procaine
side effects: proteinuria, urinary sedimentation, elevated BUN, Creatinine, and liver enzymes
adequate hydration is essential
39. Lead Chelation Succimer (DMSA)
only oral chelation agent
43-60% reduction in blood levels with fewer side effects
“rotten egg” odor
side effects: abdominal pain, N/V, diarrhea, elevated LFTs
40. Lead Chelation D-Penicillamine
reduces moderately elevated blood lead levels by 33%
only recommended for use when patients have had unacceptable reactions to DMSA and CaNa2EDTA
side effects: rash, leukopenia, thrombocytopenia, hematuria, proteinuria, eosinophilia, nephrotoxicity
contraindicated for persons with PCN allergy