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MS.LINCY SAMSON ,PBBSC ( N )
NURSING TUTOR
CHILD HEALTH NURSING
GANGA COLLEGE OF NURSING
COIMBATORE
REVIEW OF ANEMIA
Learning Objectives
At the end of the class the students will be able to
• define anemia
• list down the causes of anemia
• describe the Pathophysiology of anemia
• discuss the clinical manifestations of anemia
• state the diagnostic evaluation of anemia
• explain the management of anemia and aplastic anemia
Functions of Blood
 Transports
 Nutrients absorbed from GI tract
 O2 – from lungs to cells of whole body
 CO2 – from metabolized cells to lungs
 Wastes - from metabolized cells to kidney
 Hormones – from endocrine glands to target cells
 Body temperature control
 Maintenance of body fluid pH (Buffering action)
 Prevent blood loss (coagulation)
 Prevent diseases (phagocytosis and antibody production)
ANEMIA
INTRODUCTION
Anemia is a common blood disorder that occurs
when the body does not have enough RBCs.
RBC carry Oxygen throughout the body using a
protein called Hemoglobin. If there are not
enough of these cells or the protein results in
anemia.
DEFINITION
The term Anemia describes a condition in which
the number of Red Blood Cells(RBC) or
Hemoglobin(Hgb) concentration is reduced below
the normal values for age.
It is derived from the Greek word
“Ana” - Absent or decreased
“Emia”- Blood
CLASSIFICATION
Classification
Etiological Morphological Pathophysiological Severity
ETIOLOGICAL
BASED ON THE DISTURBANCE OF ERYTHROPOIESIS
Anemia
Decreased
production
Iron deficiency
Anemia
Bone marrow
suppression
Hemorrhage
Increased Loss
Increased
destruction
Morphological (Size
and colour of RBC)
Classification
Normocytic
(Normal cell size)
Normochromic
(Normal amount of
RBC)
Microcytic
(Smaller than
Normal cell size)
Hypochromic
( RBC)
Macrocytic
(Larger than
Normal cell size)
Hyperchromic
( RBC)
Morphological categories of Anemia
COMMON ANEMIA INCHILDREN
Iron deficiency anemia
Sickle cell anemia
A plastic anemia
Thalassemia
IRON DEFICIENCY ANEMIA
Iron deficiency is the most common micronutrient
deficiency worldwide and one of the most important public
health problems, affecting approximately 25% of the world’s
population
(WHO).The
according to the World Health Organization
most common causes of iron
efficiency in children include insufficient intake, low birth
weight and gastrointestinal losses related to excessive
intake of cow milk
DEFINITION
Lack of supplemental iron for the synthesis of
most prevalent nutritional and
disorder among infant and
hemoglobin
hematological
children
ETIOLOGY
Decreased iron stores Decreased intake
Increased losses Increased demands
ETIOLOGY cont…
• Insufficient supply of iron at birth (from mother)
• Prematurity (for full term 5-6 months they can store iron
but preterm only 2-3months )
• Insufficient intake of iron during the period ofrapid
growth (toddler)
• Impaired absorption
• Lack of vitamin C
• Blood loss
• Worm infestation
• Excessive intake of cow milk
Supply of inadequate iron
Depletion of iron stores
Depletion of serum transferrin
concentration
Sub normal Hb concentration
Sub normal oxygen carrying capacity
PATHOPHYSIOLOGY
CLINICAL MANIFESTATIONS
CLINICAL MANIFESTATIONScont..
CLINICAL MANIFESTATIONScont..
• Fatigue
• Tiredness
• restlessness
• Weakness
• Anorexia
• Failure tothrive
CLINICAL MANIFESTATIONScont..
• Poor attention span
• Learning problem
• Behavioral problem
• Slow cognitive development
• Poor school performnace
CLINICAL MANIFESTATIONScont..
• Excessive pallor of the skin, conjunctiva and
mucous membrane
• Nails become thin, brittle and flat
• Pica and atrophy of tongue papillae
CLINICAL MANIFESTATIONScont..
• In severe anemia spleen mayenlarge
• Cardiac enlargement with soft systolic murmur
• Unhappiness
• Lack of co-operation
DIAGNOSTIC EVALUATION
• Total blood count
• Peripheral bloodsmear
• Serum ferretin
• Total iron binding capacity
• Recticulocyte count
MANAGEMENT
Oral Iron therapy
 Most economical and effective
medication
 Simple salt like ferrous sulphate,
 ferrous fumarate and ferrous
gluconate,
 elemental iron in oral 6mg/kg
24hours
 supplemental iron10-50mg/kg/day
MANAGEMENT cont..
Parenteral IronTherapy
• Iron dextran complex : 50 mg/ml in 2 ml saline
• R o u t e intramuscular --- z track
method intravenous --- infusion methods
Iron: How much do we need?
Category Requirement
Preterm infants 2-4 mg/kg/day
Full terminfants 1 mg/kg day
Children 1-3 years old 7mg/day
Children 4-8 years old 10 mg/day
Children 9-13 yearsold 8 mg/day
Males 14-18 11 mg/day
Females 14-18 15 mg/day
DIETARY MANAGEMENT
NURSING MANAGEMENT
• Assist the child in developing a schedule for
daily activity and rest.
• Stress the importance of frequent rest periods.
• Monitor hemoglobin, hematocrit, RBC count,
and reticulocyte counts.
• Educate energy-conservation techniques.
• Encourage child to continue iron therapy for a
total therapy time (6 months to a year), even
when fatigue is no longer present.
NURSING MANAGEMENT
• Explain the importance of the diagnostic
procedures (such as complete blood
count), bone marrow aspiration and a
possible referral to a hematologist.
• Explain the importance of iron
replacement/supplementation.
• Educate the parents and the family
regarding foods rich in iron (organ and
other meats, leafy green vegetables,
molasses, beans).
PREVENTION
• Adequate antenatal care for the prevention of maternal
anemia and iron and folic acid supplementation to all
antenatal mother.
• Prevention of preterm delivery and control of infections in
prenatal, natal and post natal period.
PREVENTION cont..
• Introduction of semisolid and solid foods from 4 to 6
months of age as complementary feeding.
• Universal immunization to all children to prevent chronic
illness
• Iron and folic acid supplementation to the children and
adolescent girls
PREVENTION cont..
• Adequate treatment of parasitic infestations, chronic
illness.
• Improvement of living condition by avoidance of open air
defecation, environmental sanitation, hygienic measures,
balanced diet and preventing nutritional deficiencies.
PREVENTION cont…
• Encourage breastfeeding exclusively for 4-6 Months
• For 4 months an additional source of iron should be added, first as
an iron supplement, then transitioning to iron-fortified infant cereals.
• For <12 months who are not breastfed or are partially breastfed,
use only iron-fortified formulas (12 mg of iron per litre).
• For 6 Months encourage one feeding per day of foods rich in
vitamin C.
• Avoid feeding unmodified (nonformula) cow milk until age of 12
months.
• 1-5 years should also consume an adequate amount of iron-
containingfoods to meet daily requirements.
COMPLICATIONS
• Mild iron deficiency anemia usually does not
cause complications. However, left untreated
lead to the following health problems
– Heart failure
– Delayed growth and development
– Infections
NURSING DIAGNOSIS
• Fatigue related to decreased hemoglobin anddiminished
oxygen-carrying capacity of the blood.
• Parental Deficient knowledge related to the complexity of
treatment, lack of resources, or unfamiliarity with the
disease condition.
• Risk for infection related to invasion of microorganism
• Risk for bleeding related to bone marrow malfunctions
DEFINITION
Sickle cell anemia is one of a group of disease
collectively termed hemoglobinopathies, in
which normal adult Hgb is partly or completely
replaced by abnormal sickle Hgb.
Cont…
Sickle cell disease includes all those hereditary
disorders whose clinical, hematologic and
pathologic features are related to the presence
of HbS
PATHOPHYSIOLOGY
– Due to obstruction caused by the sickled
RBC’s
– increased RBC destruction
The abnormal adhesion,entanglement and
enmeshing ofrigid sickle-shaped RBC’s with
one another
Intermittently block the micro circulation
PATHOPHYSIOLOGY
Vasoocclusion
Absence of blood flow to adjacent tissues
Local hypoxia
Tissue ischemia and infaraction
PATHOPHYSIOLOGY
CLINICAL MANIFESTATIONS
• Progressive anemia
• Mild jaundice
• Fever
• Head ache
CLINICAL MANIFESTATIONScont..
Other features include
• Growth retardation
• Chronic anemia
• Possible delayed sexual maturation
• Marked susceptibility to sepsis
CLINICAL MANIFESTATIONS cont..
Vasoocclusive crisis
• Pain in areas of involvement
• Extremities-painful swelling of hands and feet(sickle
cell dactylitis or hand foot syndrome), painful joints
• Abdomen-severe pain resembling acute surgical
condition.
CLINICAL MANIFESTATIONScont..
• Cerebrum-stroke, visual disturbances
• Chest-symptoms resembling pneumonia
• Liver-obstructive jaundice
• Kidney-hematuria
• Genitalia-priapism (painful constant penile
erection)
CLINICAL MANIFESTATIONScont..
Sequestration crisis
• Pooling of large amounts of blood
• Hepatomegaly
• Spleenomegaly
• Circulatory collapse
CLINICAL MANIFESTATIONScont..
Aplastic crisis
• Diminished RBC production resulting in profond
anemia
CLINICAL MANIFESTATIONScont..
,
Effects of chronic vasoocclusive phenomena
• Heart-cardiomegaly, systolic murmurs
• Lungs-altered pulmonary function, susceptibility to
infections, pulmonary insufficiency
• Kidneys-inability to concentrate urine, enuresis
progressive renal failure
• Liver-hepatomegaly, cirrhosis, intrahepatic cholestasis
CLINICAL MANIFESTATIONScont..
• Spleen-spleenomegaly, functional reduction in splenic
activity progressing to autosplenectomy.
• Eyes –intraocular abnormalities, retinal detachment and
blindness
• Extremities-avascular necrosis of hip or shoulder,
skeletal deformities, chronic leg ulcers
• CNS-hemiparesis, seizures
DIAGNOSIS
• New born screening
• Sickle turbidity test
• Hemoglobin electrophoresis
• Peripheral smear
MANAGEMENT
Supportive and symptomatic treatment
• Rest to minimize energy expenditure and
oxygen use
MANAGEMENT cont..
• Hydration through oral and IV therapy
MANAGEMENT cont..
• Electrolyte replacement. since hypoxia results in
metabolic acidosis which also promotes sickling
MANAGEMENT cont..
• Analgesics for severe pain from vasoocclusion
MANAGEMENT cont..
• Blood replacement to treat anemia and to
reduce the viscosity of the sickled blood.
MANAGEMENT cont..
• Antibiotics to treat any existing infection.
MANAGEMENT cont..
• Stem cell transplantation
• Gene therapy
NURSING DIAGNOSIS
• Impaired tissue perfusion
• Activity intolerance
• Risk for infection
• Body image disturbances
• Ineffective family coping
• Knowledge deficit
APLASTIC ANEMIA
DEFINITION
Aplastic anemia is caused by bone marrow
depression and involved all the blood elements
resulting pancytopenia (insufficient number of
RBC’s, WBC’s and platelets. )
Cont…
• Hemopoietic failure is mediated by activated
cytotoxic T cells in blood and marrow.
• Involvement off only RBC’s is termed as hypoplastic
anemia
• Involvement of granulocytes is known as
agranulocytosis
• Involvement of platelets is known as
thrombocytopenia
CAUSES
• Aplastic anemia can be congenital as Fanconi
anemia
• Diamond-blackfan syndrome
• Dyskeratosis congenita
• TAR syndrome
CAUSES
• Acquired aplastic anemia may occur due to
• Viral infections (HIV, HB, EBV)
• Bacterial or parasitic infections
• Infilteration of malignant cells as in leukemia
• Exposure to radiation, chemicals (DDT)
• Drugs (chloramphenicol, antimetabolites)
CAUSES
• Human parvovirus infection
• Immune disorders such as eosinophilic faciitis
and hypoimmunoglobulinemia
• Industrial and house hold chemicals including
benzene and its derivatives which are found in
peroleum products, dyes, paint remover, shellac
and lacquers
CLINICAL MANIFESTATIONS
• Progressive and persistent anemia
• Weakness
• Easy fatigability
• Petechiae
• Ecchymosis
• Mucosal bleeding
• Hematuria
• GI bleeding
• Recurrent infections are common due to leukopenia
and neutropenia
• Intracranial bleeding may occur and presented as
head ache
• Irritability
• Excessive drowsiness
• Convulsions
• unconsciousness
CLINICAL MANIFESTATIONScont..
DIAGNOSTIC EVALUATION
• Blood examination
• Bone marrow study
MANAGEMENT
• Supportive care
• Bone marrow transplantation
MANAGEMENT
• Immunosuppresents
• Drugs such as cyclosporine and anti thymocyte
globulin suppress the activity of immune cells
• Corticosteroids such as methylprednisone
MANAGEMENT
• Bone marrow stimulants
• Colony stimulating factors such as
sargramostism (leukine)
• Neupogen, neulasta helps to stimulate the bone
marrow to produce new blood cells
• Blood transfusion
NURSING DIAGNOSIS
• Impaired tissue perfusion
• Activity intolerance
• Chronic pain
• Body image disturbances
• Ineffective family coping
• Knowledge deficit
Summary
 Anemia is defined as reduction of RBCs or Hgb concentration to levels
below normal for age. The nurse’s role in treatment of anemia is to
assist in establishing a diagnosis, prepare the child for laboratory test
administer prescribed medications, decrease tissue oxygen needs,
implement safety precautions, and observe for complications.The main
nursing goal in prevention of nutritional anemia is parent education
regarding correct feedingpractices.
Reference
 Marlow-Text book of PediatricNursing,
1996, Elsevier.
 Hockenberry- Wong’s Essentials ofPediatric
Nursing, 2012, Elsevier.
 Ghai, Essential paediatrics, 2009, CBS.
REVIEW OF ANEMIA
REVIEW OF ANEMIA

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REVIEW OF ANEMIA

  • 1. MS.LINCY SAMSON ,PBBSC ( N ) NURSING TUTOR CHILD HEALTH NURSING GANGA COLLEGE OF NURSING COIMBATORE
  • 3. Learning Objectives At the end of the class the students will be able to • define anemia • list down the causes of anemia • describe the Pathophysiology of anemia • discuss the clinical manifestations of anemia • state the diagnostic evaluation of anemia • explain the management of anemia and aplastic anemia
  • 4.
  • 5. Functions of Blood  Transports  Nutrients absorbed from GI tract  O2 – from lungs to cells of whole body  CO2 – from metabolized cells to lungs  Wastes - from metabolized cells to kidney  Hormones – from endocrine glands to target cells  Body temperature control  Maintenance of body fluid pH (Buffering action)  Prevent blood loss (coagulation)  Prevent diseases (phagocytosis and antibody production)
  • 7. INTRODUCTION Anemia is a common blood disorder that occurs when the body does not have enough RBCs. RBC carry Oxygen throughout the body using a protein called Hemoglobin. If there are not enough of these cells or the protein results in anemia.
  • 8. DEFINITION The term Anemia describes a condition in which the number of Red Blood Cells(RBC) or Hemoglobin(Hgb) concentration is reduced below the normal values for age. It is derived from the Greek word “Ana” - Absent or decreased “Emia”- Blood
  • 10. ETIOLOGICAL BASED ON THE DISTURBANCE OF ERYTHROPOIESIS Anemia Decreased production Iron deficiency Anemia Bone marrow suppression Hemorrhage Increased Loss Increased destruction
  • 11. Morphological (Size and colour of RBC) Classification Normocytic (Normal cell size) Normochromic (Normal amount of RBC) Microcytic (Smaller than Normal cell size) Hypochromic ( RBC) Macrocytic (Larger than Normal cell size) Hyperchromic ( RBC)
  • 13. COMMON ANEMIA INCHILDREN Iron deficiency anemia Sickle cell anemia A plastic anemia Thalassemia
  • 14. IRON DEFICIENCY ANEMIA Iron deficiency is the most common micronutrient deficiency worldwide and one of the most important public health problems, affecting approximately 25% of the world’s population (WHO).The according to the World Health Organization most common causes of iron efficiency in children include insufficient intake, low birth weight and gastrointestinal losses related to excessive intake of cow milk
  • 15. DEFINITION Lack of supplemental iron for the synthesis of most prevalent nutritional and disorder among infant and hemoglobin hematological children
  • 16. ETIOLOGY Decreased iron stores Decreased intake Increased losses Increased demands
  • 17. ETIOLOGY cont… • Insufficient supply of iron at birth (from mother) • Prematurity (for full term 5-6 months they can store iron but preterm only 2-3months ) • Insufficient intake of iron during the period ofrapid growth (toddler) • Impaired absorption • Lack of vitamin C • Blood loss • Worm infestation • Excessive intake of cow milk
  • 18. Supply of inadequate iron Depletion of iron stores Depletion of serum transferrin concentration Sub normal Hb concentration Sub normal oxygen carrying capacity PATHOPHYSIOLOGY
  • 21. CLINICAL MANIFESTATIONScont.. • Fatigue • Tiredness • restlessness • Weakness • Anorexia • Failure tothrive
  • 22. CLINICAL MANIFESTATIONScont.. • Poor attention span • Learning problem • Behavioral problem • Slow cognitive development • Poor school performnace
  • 23. CLINICAL MANIFESTATIONScont.. • Excessive pallor of the skin, conjunctiva and mucous membrane • Nails become thin, brittle and flat • Pica and atrophy of tongue papillae
  • 24. CLINICAL MANIFESTATIONScont.. • In severe anemia spleen mayenlarge • Cardiac enlargement with soft systolic murmur • Unhappiness • Lack of co-operation
  • 25. DIAGNOSTIC EVALUATION • Total blood count • Peripheral bloodsmear • Serum ferretin • Total iron binding capacity • Recticulocyte count
  • 26. MANAGEMENT Oral Iron therapy  Most economical and effective medication  Simple salt like ferrous sulphate,  ferrous fumarate and ferrous gluconate,  elemental iron in oral 6mg/kg 24hours  supplemental iron10-50mg/kg/day
  • 27. MANAGEMENT cont.. Parenteral IronTherapy • Iron dextran complex : 50 mg/ml in 2 ml saline • R o u t e intramuscular --- z track method intravenous --- infusion methods
  • 28. Iron: How much do we need? Category Requirement Preterm infants 2-4 mg/kg/day Full terminfants 1 mg/kg day Children 1-3 years old 7mg/day Children 4-8 years old 10 mg/day Children 9-13 yearsold 8 mg/day Males 14-18 11 mg/day Females 14-18 15 mg/day
  • 30. NURSING MANAGEMENT • Assist the child in developing a schedule for daily activity and rest. • Stress the importance of frequent rest periods. • Monitor hemoglobin, hematocrit, RBC count, and reticulocyte counts. • Educate energy-conservation techniques. • Encourage child to continue iron therapy for a total therapy time (6 months to a year), even when fatigue is no longer present.
  • 31. NURSING MANAGEMENT • Explain the importance of the diagnostic procedures (such as complete blood count), bone marrow aspiration and a possible referral to a hematologist. • Explain the importance of iron replacement/supplementation. • Educate the parents and the family regarding foods rich in iron (organ and other meats, leafy green vegetables, molasses, beans).
  • 32. PREVENTION • Adequate antenatal care for the prevention of maternal anemia and iron and folic acid supplementation to all antenatal mother. • Prevention of preterm delivery and control of infections in prenatal, natal and post natal period.
  • 33. PREVENTION cont.. • Introduction of semisolid and solid foods from 4 to 6 months of age as complementary feeding. • Universal immunization to all children to prevent chronic illness • Iron and folic acid supplementation to the children and adolescent girls
  • 34. PREVENTION cont.. • Adequate treatment of parasitic infestations, chronic illness. • Improvement of living condition by avoidance of open air defecation, environmental sanitation, hygienic measures, balanced diet and preventing nutritional deficiencies.
  • 35. PREVENTION cont… • Encourage breastfeeding exclusively for 4-6 Months • For 4 months an additional source of iron should be added, first as an iron supplement, then transitioning to iron-fortified infant cereals. • For <12 months who are not breastfed or are partially breastfed, use only iron-fortified formulas (12 mg of iron per litre). • For 6 Months encourage one feeding per day of foods rich in vitamin C. • Avoid feeding unmodified (nonformula) cow milk until age of 12 months. • 1-5 years should also consume an adequate amount of iron- containingfoods to meet daily requirements.
  • 36. COMPLICATIONS • Mild iron deficiency anemia usually does not cause complications. However, left untreated lead to the following health problems – Heart failure – Delayed growth and development – Infections
  • 37. NURSING DIAGNOSIS • Fatigue related to decreased hemoglobin anddiminished oxygen-carrying capacity of the blood. • Parental Deficient knowledge related to the complexity of treatment, lack of resources, or unfamiliarity with the disease condition. • Risk for infection related to invasion of microorganism • Risk for bleeding related to bone marrow malfunctions
  • 38.
  • 39. DEFINITION Sickle cell anemia is one of a group of disease collectively termed hemoglobinopathies, in which normal adult Hgb is partly or completely replaced by abnormal sickle Hgb.
  • 40. Cont… Sickle cell disease includes all those hereditary disorders whose clinical, hematologic and pathologic features are related to the presence of HbS
  • 41. PATHOPHYSIOLOGY – Due to obstruction caused by the sickled RBC’s – increased RBC destruction The abnormal adhesion,entanglement and enmeshing ofrigid sickle-shaped RBC’s with one another Intermittently block the micro circulation
  • 42. PATHOPHYSIOLOGY Vasoocclusion Absence of blood flow to adjacent tissues Local hypoxia Tissue ischemia and infaraction
  • 44. CLINICAL MANIFESTATIONS • Progressive anemia • Mild jaundice • Fever • Head ache
  • 45. CLINICAL MANIFESTATIONScont.. Other features include • Growth retardation • Chronic anemia • Possible delayed sexual maturation • Marked susceptibility to sepsis
  • 46. CLINICAL MANIFESTATIONS cont.. Vasoocclusive crisis • Pain in areas of involvement • Extremities-painful swelling of hands and feet(sickle cell dactylitis or hand foot syndrome), painful joints • Abdomen-severe pain resembling acute surgical condition.
  • 47. CLINICAL MANIFESTATIONScont.. • Cerebrum-stroke, visual disturbances • Chest-symptoms resembling pneumonia • Liver-obstructive jaundice • Kidney-hematuria • Genitalia-priapism (painful constant penile erection)
  • 48. CLINICAL MANIFESTATIONScont.. Sequestration crisis • Pooling of large amounts of blood • Hepatomegaly • Spleenomegaly • Circulatory collapse
  • 49. CLINICAL MANIFESTATIONScont.. Aplastic crisis • Diminished RBC production resulting in profond anemia
  • 50. CLINICAL MANIFESTATIONScont.. , Effects of chronic vasoocclusive phenomena • Heart-cardiomegaly, systolic murmurs • Lungs-altered pulmonary function, susceptibility to infections, pulmonary insufficiency • Kidneys-inability to concentrate urine, enuresis progressive renal failure • Liver-hepatomegaly, cirrhosis, intrahepatic cholestasis
  • 51. CLINICAL MANIFESTATIONScont.. • Spleen-spleenomegaly, functional reduction in splenic activity progressing to autosplenectomy. • Eyes –intraocular abnormalities, retinal detachment and blindness • Extremities-avascular necrosis of hip or shoulder, skeletal deformities, chronic leg ulcers • CNS-hemiparesis, seizures
  • 52. DIAGNOSIS • New born screening • Sickle turbidity test • Hemoglobin electrophoresis • Peripheral smear
  • 53. MANAGEMENT Supportive and symptomatic treatment • Rest to minimize energy expenditure and oxygen use
  • 54. MANAGEMENT cont.. • Hydration through oral and IV therapy
  • 55. MANAGEMENT cont.. • Electrolyte replacement. since hypoxia results in metabolic acidosis which also promotes sickling
  • 56. MANAGEMENT cont.. • Analgesics for severe pain from vasoocclusion
  • 57. MANAGEMENT cont.. • Blood replacement to treat anemia and to reduce the viscosity of the sickled blood.
  • 58. MANAGEMENT cont.. • Antibiotics to treat any existing infection.
  • 59. MANAGEMENT cont.. • Stem cell transplantation • Gene therapy
  • 60. NURSING DIAGNOSIS • Impaired tissue perfusion • Activity intolerance • Risk for infection • Body image disturbances • Ineffective family coping • Knowledge deficit
  • 62. DEFINITION Aplastic anemia is caused by bone marrow depression and involved all the blood elements resulting pancytopenia (insufficient number of RBC’s, WBC’s and platelets. )
  • 63. Cont… • Hemopoietic failure is mediated by activated cytotoxic T cells in blood and marrow. • Involvement off only RBC’s is termed as hypoplastic anemia • Involvement of granulocytes is known as agranulocytosis • Involvement of platelets is known as thrombocytopenia
  • 64. CAUSES • Aplastic anemia can be congenital as Fanconi anemia • Diamond-blackfan syndrome • Dyskeratosis congenita • TAR syndrome
  • 65. CAUSES • Acquired aplastic anemia may occur due to • Viral infections (HIV, HB, EBV) • Bacterial or parasitic infections • Infilteration of malignant cells as in leukemia • Exposure to radiation, chemicals (DDT) • Drugs (chloramphenicol, antimetabolites)
  • 66. CAUSES • Human parvovirus infection • Immune disorders such as eosinophilic faciitis and hypoimmunoglobulinemia • Industrial and house hold chemicals including benzene and its derivatives which are found in peroleum products, dyes, paint remover, shellac and lacquers
  • 67. CLINICAL MANIFESTATIONS • Progressive and persistent anemia • Weakness • Easy fatigability • Petechiae • Ecchymosis • Mucosal bleeding • Hematuria • GI bleeding
  • 68. • Recurrent infections are common due to leukopenia and neutropenia • Intracranial bleeding may occur and presented as head ache • Irritability • Excessive drowsiness • Convulsions • unconsciousness CLINICAL MANIFESTATIONScont..
  • 69. DIAGNOSTIC EVALUATION • Blood examination • Bone marrow study
  • 70. MANAGEMENT • Supportive care • Bone marrow transplantation
  • 71. MANAGEMENT • Immunosuppresents • Drugs such as cyclosporine and anti thymocyte globulin suppress the activity of immune cells • Corticosteroids such as methylprednisone
  • 72. MANAGEMENT • Bone marrow stimulants • Colony stimulating factors such as sargramostism (leukine) • Neupogen, neulasta helps to stimulate the bone marrow to produce new blood cells • Blood transfusion
  • 73. NURSING DIAGNOSIS • Impaired tissue perfusion • Activity intolerance • Chronic pain • Body image disturbances • Ineffective family coping • Knowledge deficit
  • 74. Summary  Anemia is defined as reduction of RBCs or Hgb concentration to levels below normal for age. The nurse’s role in treatment of anemia is to assist in establishing a diagnosis, prepare the child for laboratory test administer prescribed medications, decrease tissue oxygen needs, implement safety precautions, and observe for complications.The main nursing goal in prevention of nutritional anemia is parent education regarding correct feedingpractices.
  • 75. Reference  Marlow-Text book of PediatricNursing, 1996, Elsevier.  Hockenberry- Wong’s Essentials ofPediatric Nursing, 2012, Elsevier.  Ghai, Essential paediatrics, 2009, CBS.