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Hematological Conditions in Children Nursing Assessment and Interventions Kathryn Kushto- Reese

Sickle cell anemia summer 2013

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Page 1: Sickle cell anemia summer 2013

Hematological Conditions in Children

Nursing Assessment and Interventions

Kathryn Kushto-Reese

Page 2: Sickle cell anemia summer 2013

Sickle Cell Disease

Inherited: autosomal recessive Hemoglobin (Hgb A) replaced by

abnormal sickle hemoglobin (Hgb S)

Valine (amino acid) substituted for glutamic acid on beta chain of Hgb molecule

Page 3: Sickle cell anemia summer 2013

Course of DiseaseCourse of Disease

In healthy infants at about 6 In healthy infants at about 6 months months

–normally fetal hemoglobin is normally fetal hemoglobin is replaced by normal HbAreplaced by normal HbA

In infant with sickle cell disease, In infant with sickle cell disease, HbA replaced by HbSHbA replaced by HbS

Page 4: Sickle cell anemia summer 2013

PathophysiologyPathophysiology

EITHER:EITHER:–decrease in oxygen tension decrease in oxygen tension

( hypoxemia) ( hypoxemia)

OROR–decrease in blood pH ( metabolic decrease in blood pH ( metabolic

acidosis)acidosis) Causes RBCs to lose their normal shapeCauses RBCs to lose their normal shape

Page 5: Sickle cell anemia summer 2013

Normal and Sickle CellsNormal and Sickle Cells

Page 6: Sickle cell anemia summer 2013

Normal & Sickle RBCsNormal & Sickle RBCs

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Sickled CellsSickled Cells

Have a short life span Lodge in small capillaries, break apart Increase the viscosity of blood

–slows circulation–occlude vessels –cause tissue ischemia

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Things that Cause Changes in Things that Cause Changes in Oxygen Tension or Blood pHOxygen Tension or Blood pH

Fever Infection Dehydration Hypoxia Acidosis Extreme Exercise Serious Cold Exposure High Altitudes

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SUMMER CAMPSUMMER CAMP

Page 10: Sickle cell anemia summer 2013

Organ Systems AffectedOrgan Systems Affected SpleenSpleen: infection, : infection,

sequestrationsequestration LiverLiver: enlargement, : enlargement,

gallstones, jaundicegallstones, jaundice BonesBones: osteoporosis, : osteoporosis,

lordosis, kyphosis, lordosis, kyphosis, aseptic necrosis of aseptic necrosis of head of the femur head of the femur

SkinSkin: ulcers: ulcers

KidneysKidneys: necrosis, : necrosis, scarringscarring

CNSCNS: stroke, : stroke, paralysisparalysis

EyesEyes: blindness, : blindness, hemorrhagehemorrhage

CVCV: cardiomegaly, : cardiomegaly, murmurmurmur

LungsLungs: “chest : “chest syndrome”, infectionsyndrome”, infection

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Complications of SCDComplications of SCD

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OstoearthrosisOstoearthrosis

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Chronic ComplicationsChronic Complications

Icteric sclera / jaundice Anorexia Infection Growth retardation Delayed puberty Bone and joint problems

Page 14: Sickle cell anemia summer 2013

Types of Sickle Cell CrisesTypes of Sickle Cell Crises Most common type of Sickle Cell

Crisis Vaso-occlusive (VOC) Potentially Life Threatening Acute Chest Syndrome Splenic Sequestration( blood

trapped in spleen→CV collapse

Page 15: Sickle cell anemia summer 2013

Clinical SymptomsClinical SymptomsVOC CrisisVOC Crisis

PAIN: extremely painful, swelling of PAIN: extremely painful, swelling of joints in hands and feet (Hand and foot joints in hands and feet (Hand and foot syndrome), severe abdominal pain.syndrome), severe abdominal pain.

FeverFever ANEMIAANEMIA

–hemoglobin of 5.5 to 9.5 g/dlhemoglobin of 5.5 to 9.5 g/dl–hematocrit of 19-29 %hematocrit of 19-29 %–Reticulocyte count > 2.5 %Reticulocyte count > 2.5 %

Fever, pneumoniaFever, pneumonia HematuriaHematuria

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Management: Vaso-occlusive Management: Vaso-occlusive CrisisCrisis

PAIN MANAGEMENT Bed rest Oxygen Hydration ( 1.5-2 x maintenance fluid) Balance electrolytes Antibiotics for infection Blood transfusions

Page 17: Sickle cell anemia summer 2013

Acute Chest SyndromeAcute Chest Syndrome

Leading cause of morbidity and Leading cause of morbidity and mortality.mortality.

Presence of a new pulmonary infiltrate Presence of a new pulmonary infiltrate associated with:associated with:– severe chest painsevere chest pain– feverfever– cough, dyspnea, tachypneacough, dyspnea, tachypnea– wheezing, retractionswheezing, retractions– Hypoxia and severe anemiaHypoxia and severe anemia

Page 18: Sickle cell anemia summer 2013

Acute Chest SyndromeAcute Chest Syndrome

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Management of Acute chest Syndrome

Pain Management Oxygen Hydration Pulse oximetry monitoring VS measurement and assessment of BS, WOB, IS

and cough and deep breathing PFT,s Antibiotics Transfusion for severe hypoxemia, anemia

Page 20: Sickle cell anemia summer 2013

HydroxyureaHydroxyurea

Increases amount of HbgF Increases amount of HbgF (mechanism is unknown) (mechanism is unknown)

Decreases number of hospitalizations Decreases number of hospitalizations and episodes of pneumonia , and episodes of pneumonia , posssibly CVA’sposssibly CVA’s

Used in children with > 3 episodes of Used in children with > 3 episodes of VOC requiring hospitalization per year VOC requiring hospitalization per year or recurrent episodes of Chest or recurrent episodes of Chest Syndrome, and history of CVA’s Syndrome, and history of CVA’s

Page 21: Sickle cell anemia summer 2013

Risks of HydroxyureaRisks of Hydroxyurea

Decreases blood counts– blood work every 2 weeks until dosage is

finalized

Can cause infection and bleeding Small risk of cancer or leukemia when

used for several years Teratogenic

Page 22: Sickle cell anemia summer 2013

Nursing DiagnosesNursing Diagnoses Acute pain related to tissue ischemia Acute pain related to tissue ischemia Risk for Infection related to compromised splenic function Risk for Infection related to compromised splenic function Activity intolerance related to pain Activity intolerance related to pain Deficient fluid volume related to increased fluid Deficient fluid volume related to increased fluid

requirements and po limitationsrequirements and po limitations Risk of ineffective peripheral tissue perfusion related to Risk of ineffective peripheral tissue perfusion related to

decreased capillary blood supplydecreased capillary blood supply Fatigue related to inadequate tissue oxygenation Fatigue related to inadequate tissue oxygenation Anxiety related to unfamiliar hospital environment Anxiety related to unfamiliar hospital environment Interrupted family processes related to caring for a child Interrupted family processes related to caring for a child

with a chronic condition with a chronic condition

Page 23: Sickle cell anemia summer 2013

Diagnostic TestsDiagnostic Tests

Hemoglobin ElectrophoresisHemoglobin Electrophoresis (from newborns cord blood)(from newborns cord blood) Sickle-turbidity test (Sickledex) Sickle-turbidity test (Sickledex) ( quick screening > 6 months after fetal ( quick screening > 6 months after fetal

Hgb levels fallHgb levels fall CBC, for drop Hgb and high CBC, for drop Hgb and high

reticulocyte countreticulocyte count

Page 24: Sickle cell anemia summer 2013

EARLY DETECTIONEARLY DETECTION

Page 25: Sickle cell anemia summer 2013

Newborn Screening

Mandated in all 50 states and D.C.Mandated in all 50 states and D.C. Evidence based practice shows that early detection Evidence based practice shows that early detection

and treatment can prevent life threatening and treatment can prevent life threatening pneumococcal infections.pneumococcal infections.

(USPSTF ( 2007).(USPSTF ( 2007). Helpful because parents can start penicillin Helpful because parents can start penicillin

prophylaxis by 2 months of age in affected infants prophylaxis by 2 months of age in affected infants and pneumococcal conjugate vaccinations and and pneumococcal conjugate vaccinations and parental education about early warning signs of parental education about early warning signs of infectioninfection

Page 26: Sickle cell anemia summer 2013

Well Child CareWell Child Care

Nutrition ( folic acid supplements) Adequate hydration Infection prevention Immunizations (vaccines) (Given to High risk children with underlying medical

conditions.)

– Pneumococcal ( PCV-13, PPSV)– Meningococcal ( MCV4)– Influenza vaccine ( yearly)