Atopic dermatitis (eczema)
♦ Inflammation of epidermis
Care goals
S/S
Interventions
** A child with any integumentary disorders needs to be monitored for signs of superficial and systemic infection.**
Impetigo
♦ Contagious bacterial infection of the skin caused by beta-hemolytic strep or staph
S/S:
Interventions
Pediculosis Capitis (lice)
♦ The infestation of hair and scalp with lice
♦ Nits = eggs (white)
♦ Adult lice are harder to see – small tan or gray specs that move quickly
Interventions
Scabies
♦ Parasite burrows in skin, spread by close contact.
♦ Infectious during entire course of infection.
♦ Host mite dies after 4-5 weeks in burrow but eggs hatch in 3-5d and mature to complete life cycle.
S/S
Interventions
Pediatric Burns
♦ Lower temps and shorter exposure can cause a more severe burn in a child b/c skin is thinner
♦ Severely burned children at risk of
♦ Higher proportion of body fluid to mass puts kids at increased risk of CV complications
♦ Scarring is more severe in children; may delay growth
♦ Fluid replacement always needed in first 24-hr. (especially if more than 10% of TBSA burned)
Interventions
Sickle Cell Anemia
♦ Hemoglobin A is partly or completely replaced by abnormal sickle hemoglobin S
♦ Sickledex (sickle-turbidity test) can be done with finger stick and produces results in 3 min – positive result requires confirmation via hemoglobin electrophoresis to distinguish a carrier from someone with the disease
** Hemoglobin S is sensitive to changes in the O2 content of the RBC **
Situational precursors
Interventions
Sickle Cell Vaso-Occlusive Crisis
Caused by stasis of blood w/ clumping of cells in the microcirculation, ischemia and infarction Manifestations: -fever -painful swelling of hands, feet, and joints -abdominal pain
Sickle cell Splenic Sequestration
Caused by pooling and clumping of blood in the spleen (hypersplenism) Manifestations: profound anemia, hypovolemia, and shock
Sickle Cell Hyperhemolytic crisis
An accelerated rate of RBC destruction
Manifestations: anemia, jaundice, reticulocytosis
Sickle Cell Aplastic crisis
Caused by diminished production and increased destruction of RBCs, triggered by viral infection or depletion of folic acid Manifestations: profound anemia and pallor
Iron-deficiency anemia
Causes
S/S
Interventions
Iron-rich foods
Aplastic Anemia
♦ Deficiency of circulating erythrocytes and all other formed elements of blood, resulting in the arrested development of cells within the bone marrow
S/S
Therapeutic management
Hemophilia
Clotting deficiency: VIII (A, Classic), IX (B, Christmas) Primary tx: clotting factor replacement ID w/ abnormal bleeding with trauma/surgery (sometimes first detected after circumcision), nosebleeds, joint bleeding that causes pain, tenderness, swelling, limited ROM, bruis easy. Tests show Platelet, Hgb, Hct is normal, clotting factor function abnormal (so prolonged PTT). Immobilize affected extremity if there is joint pain, elevate, apply ice. If active bleed apply pressure 15min. Assess neuro status (risk of intracranial hemorrhage), monitor urine for hematuria. Avoid contact sports. Wear protection gear while learning to walk or participating in sports (helmet, knees/elbows). MAKE THEM SWIMMERS! Should have medic-alert bracelet!!!
von Willebrand’s disease
Deficiency of protein by same name
Characterized by tendency to bleed from mucous membranes
The d/o causes platelets to adhere to dmg’d endothelium.
SEE: nosebleed, gum bleeding, easy bruising, excessive menstrual bleed
Tx: similar to hemophilia, factor replacement
Should have medic-alert bracelet!!!
Beta Thalassemia Major
Autosomal recessive disorder (both parents must be carriers)
Highest incidence in individuals of Mediterranean descent
Reduced production of 1 of the globin chains in the synthesis of Hgb
Tx is supportive – goal of therapy is to maintain normal hemoglobin levels by the administration of blood transfusions
Monitor for iron overload; chelation therapy may be necessary
Iron administration
-Best on empty stomach 1 hr before meals or 2 hr after. -Give with multivitamin or Vit C to help w/ absorption -Don’t give w/ milk or antacids (decr absorption) -Give liquid iron in straw and rinse mouth or brush teeth after -Tell parents that stools will be black, can cause constipation and has foul aftertaste
Normal child temperature vs Fever s/s
Tx: can give ibuprofen/Motrin
(not ASA (aspirin) b/c of Reye’s syndrome which seems to occur when given for flu or chicken pox as well)
~ Reye’s is a sudden acute brain damage and liver function problem
Moderate dehydration
increased pulse, RR, irritable/more thirsty, dry mucous membranes, decreased tears, sunken anterior fontanel, slowed cap refill
PKU (Phenylketonuria)
♦ Genetic disorder that results in central nervous system damage from toxic levels of phenylalanine (and essential amino acid) in the blood
♦ Test done w/in first 48 hrs of life after baby has started formula or breastmilk
♦ Required by all 50 states
♦ Tests for phenylalanine in the blood, toxic levels > 20 mg/dL
♦ Causes dmg to CNS
TESTING: after NB has begun formula or breastfeeding
♦ Assessment in all children: -digestive issues and vomiting -seizures -musty odor of the urine -mental retardation
♦ Assessment in older children: -Eczema -Hypertonia -Hypopigmentation of the hair, skin, and irises -hyperactive behavior
♦ Foods to restrict (that have phenylalanine): -meats and diary -aspartame
Leukemia: General
♦ Malignant increase in # of leukocytes (usually at an immature stage) in the bone marrow
♦ Proliferating immature WBCs depress the bone marrow, causing anemia from decreased erythrocytes, infection from neutropenia, and bleeding from thrombocytopenia
♦ S/S: fever, pallor, fatigue, anorexia, hemorrhage (usually petechiae), bone and joint pain
♦ WBC count could be normal, elevated, or depressed depending on presence of infection or #s of immature vs mature cells
♦ Diagnostic test: bone marrow biopsy
Hodgkin’s Disease
♦ Malignancy of the lymph nodes that originates in a single lymph node or a single chain – metastasizes to nonnodal sites, esp. spleen, liver, bone marrow, lungs, medistinum
♦ Characterized by presence of Reed-Sternberg cells in lymph node biopsy
♦ Generally good prognosis
Wilms’ Tumor (Nephroblastoma)
♦ Most common intraabdominal and kidney tumor of childhood
♦ S/S: swelling or mass in the abdomen (firm, nontender, deep); urinary retention; anemia (from hemorrhage in tumor); pallor, anorexia, fatigue (from anemia); hypertension (due to secretion of renin from tumor); weight loss; fever
♦ Avoid palpating the abdomen!!
♦ Measure abdominal girth daily
Brain Tumors
♦ Often characterized by a headache that is worst upon awakening and improves throughout the day