Professional Documents
Culture Documents
PEDIATRIC NURSING
the application of nursing knowledge in the psychomotor, psychosocial and cognitive
development of children and the utilization of nursing process in the care of clients from birth to
adolescence period.
Definition of Terms
Growth: Increase in size of a structure. Human growth is orderly and predictable, but not even; it follows
a cyclical pattern.
Development: Maturation of physiologic and psychosocial systems to more complex state.
Phylogeny: Development or evolution of a species or group; a pattern of development for a species
Ontogeny: Development of an individual within a species
6 - 12 years Latency: Energy used to gain new skills INDUSTRY vs. INFERIORITY 5. EARLY ADOLESCENCE MIDDLE CHILDHOOD
in social relationships and knowledge Significant relations: NEIGHBORHOOD - Learns independence and - Learning physical skills
Behaviors: and SCHOOL how to relate to opposite necessary for games
- Sense of industry and mastery Psychosocial virtues: Competence sex - Learning to get along
- Learns control over aggressive Mal-adaptations and malignancies: with age – mates
destructive impulses Narrow virtuosity - inertia - Achieving personal
- Acquires friends independence
- Learning appropriate
Theories PSYCHOSEXUAL MODEL (Freud) PSYCHOSOCIAL MODEL (Erikson) INTERPERSONAL MODEL DEVELOPMENTAL TASK
(Sullivan) (Havighurst)
masculine or feminine
social roles
12 – 18 years Genital: Sexual pleasure through IDENTITY vs. ROLE CONFUSION 6. LATE ADOLESCENCE / ADOLESCENCE
genitals Significant relations: PEER GROUPS and YOUNG ADULT - Achieving new and more
Behaviors: ROLE MODEL - Develops intimate mature relations with age
- Becomes independent of Psychosocial virtues: Fidelity and relationship with person of mates or both sexes
parents Loyalty the opposite sex - Accepting one’s physique
- Responsible for self Mal-adaptations and malignancies: - Becomes economically, and using the body
- Develops sexual identity, Fanaticism - repudiation intellectually and effectively
ability to love and work emotionally self-sufficient - Achieving emotional
independence from
parents and other adults
- Selecting and preparing
for an occupation
- Preparing for marriage
and family life
18 – 25 years INTIMACY vs. ISOLATION 7. MIDDLE AGE EARLY ADULTHOOD
Significant relations: PARTNERS and - Learns to be - Selecting a mate
FRIENDS interdependent and - Learning to live with a
Psychosocial virtues: Love assumes responsibility for partner
Mal-adaptations and malignancies: others - Starting a family
Promiscuity – exclusivity - Rearing Children
- Managing a home
Theories PSYCHOSEXUAL MODEL (Freud) PSYCHOSOCIAL MODEL (Erikson) INTERPERSONAL MODEL DEVELOPMENTAL TASK
(Sullivan) (Havighurst)
- Getting started in an
occupation
- Taking on civic
responsibilities
- Finding a congenial social
group
6 - 12 months
Breast milk or formula continues to be primary source of nutrition.
Introduction of solid foods starts with cereal (usually rice cereal), which is continued until 18
months.
Introduction of other food is arbitrary; most common sequence is fruits, vegetables, meats.
Decrease amount of formula to about 30 oz. as foods are added.
Iron supplementation can be stopped.
Finger foods such as cheese, meat, carrots can be started around 10 months.
Chopped table food or junior food can be introduced by 12 months
Weaning from breast or bottle to cup should be gradual during second 6 months. NURSING ALERT:
Introduce one
b. TODDLER new food a week
to assess for food
Caloric requirement is approximately 100 calories/kg/day allergy
Increased need for calcium, iron, and phosphorus.
Needs 16 - 24 oz milk/day.
Appetite decreases
Able to feed self.
Negativism may interfere with eating.
Initial dental examination at 3 years.
c. PRE-SCHOOL
Caloric needs diminish in relation to body size: 85 kcal/kg/day
“Junk” food may become a problem; excess sugar, starches, fat.
Obesity is a risk in this age group.
Nutrition education should be integrated into school program.
d. SCHOOL-AGE
Boys requires more calories
Increased need for Iron during pre-pubertal period
Adequate Calcium intake to ensure good teeth
Involve children in planning and preparing meals
e. ADOLESCENT
Nutritional requirements peak during years of maximum growth: age 10-12 in girls, 2 years later in
boys
Appetite increases.
Inadequate diet can retard growth and delay sexual maturation.
Food intake needs to be balanced with energy expenditure
Increased needs include calcium for skeletal growth
IRON for increased muscle mass and blood cell development.
ZINC for development of skeletal and muscle tissue and sexual maturation.
AGE FEARS
3. The unknown
Table 1.4 Childhood Fears
N o” attitude
E xplores genitals
E elimination training (Bowel Training)
D evelopmental task : autonomy vs shame and doubt
S eparation anxiety
P arallel play
R ituals and routines
A ccident – prone
I nvolve parents in child care
S ibling rivalry
E xplain procedures
A lways active
G rows steadily
E xplain pre-pubertal changes
P romote safety
A ttachment to opposite sex
I dentity vs. role confusion/diffusion
R espect Independece
S ubstance abuse must be addressed.
B. Anthropometric Measurements:
Weight - 2,500 – 4,000 g
Length -18 – 21 inches
Head Circumference -13 – 14 inches / 33- 35 cm.
Chest Circumference -12 – 13 inches / 30 – 33 cm.
C. Gestational Age
Preterm - more than 20 weeks but less than 38 weeks AOG
Term – 38 -40 weeks AOG
Postterm – 40 weeks and above
FEMALE: EXTERNAL
STRUCTURES Doesn’t cover the Slightly covering Completely covers
( Labial folds) clitoris the clitoris the clitoris
(d) SKIN
NORMAL DEVIATIONS FROM NORMAL
SKIN Pink all over the body Central Cyanosis –
Acrocyanosis – blue extremities; due indicates decreased
to immature peripheral circulation oxygenation or airway
obstruction
Pallor – indicative of
anemia due to
excessive blood loss;
dec. iron stores of fetus
Gray Skin – indicative of Infection.
Refer ASAP
Pathologic Jaundice – occurs within
the 1st 24 hours
- indicative of Rh/ ABO
Incompatibility, Hemolysis
Period of Reactivity
30 minutes after birth
Awake and active
VS are increased
Mother infant bonding: breastfeeding and rooming-in of infant
Resting Period
2 to 4 hours
VS returning to baseline
1 ½ sleep and difficult to be aroused
(c) BRONCHITIS
infection of the major bronchi
Assessment:
cough, worse at night; becomes productive
in 2-3 days
Implementation:
Monitor for respiratory distress
Increased fluid intake
Acetaminophen as ordered
(e) PNEUMONIA
inflammation of the alveoli
inhalation of causative agent à bloodstream
Primary atypical pneumonia – most common cause of
pneumonia between 5-12 years
Implementation:
antimicrobial therapy
Oxygen
cool humidification
encourage child to lie on the affected side
isolation procedures as needed
Antipyretics
IVF; liberal fluid intake
(f) ASTHMA
chronic inflammatory disease of airways
commonly caused by physical and chemical irritants common
symptoms – coughing in the absence of respiratory infection, especially at night
Assessment:
episodes of wheezing, breathlessness, dyspnea, chest tightness
SOB, cough, wheezing
child speaks in short, broken phrases
retractions
exercise induced bronchospasm
severe spasm or obstruction
Implementation:
continuously monitor respiratory status
administer quick-relief (rescue) medication
initiate an IV line; prepare to correct
dehydration, acidosis or electrolyte imbalance
Medications
Quick relief
To treat symptoms and exacerbations
Short acting beta 2 agonists
Anticholinergics – for relief of acute
bronchospasm (ipratropium bromide)
Long term control
Corticosteroids
Long acting b2 agonist
Long acting bronchodilator
Nebulizer, MDI ( metered dose inhaler)
Used to deliver many medications
Non-CFC (chlorofluorocarbon) – albuterol
Chest physiotherapy
Includes breathing exercises
Home care measures:
instruct in measures to eliminate allergens
avoid extremes of environmental temperature
avoid exposure to individuals with a viral infection
instruct the child in how to recognize early symptoms
instruct the child in the cleaning of devices used for inhaled medications
keep immunization up to date
Implementation:
Require emergency medical treatment
Cardiac catheterization
Balloon atrial septostomy
Prognosis:
Spontaneous closure after infancy rarely occurs
Without treatment – life expectancy short
Management:
Oral of IV Indomethacin (prostaglandin inhibitor) to promote ductus closure
Interventional cardiac catheterization with Dacron coated stainless coil insertion by
6 mos to 1 year
Surgical closure by ductal ligation
CARDIAC SURGERY
Postoperatively:
Monitor for signs of discomfort
Monitor for signs of sepsis (fever, lethargy, diaphoresis, altered LOC)
Monitor lines, tubes or catheters ; remove promptly
Administer pain medications; note effectiveness
Encourage rest periods
Facilitate parent-child contact as soon as possible
Home Care
omit activities in which child could fall for 2-4 weeks
avoid crowds for 2 weeks after discharge
no added salt diet
do not put creams, lotions or powders on the incision site
child may return to school 3rd week after discharge
no physical education for 2 months
follow up check-up 2 weeks after hospitalization
avoid immunizations, invasive procedure and dental visits for 2 months
advise parents regarding importance of dental visit every 6 month
Assessment:
tachycardia
tachypnea
profuse scalp sweating especially in infants
fatigue and irritability
sudden weight gain
respiratory distress
Management:
Goal of treatment: To improve cardiac function, remove accumulated fluid and sodium, decrease
cardiac demands, improve tissue oxygenation
Asssessment:
Signs of carditis: SOB, edema of the face, abdomen or ankles, precordial pain
Signs of polyarthritis: edema, inflammation of the large joints, joint pain
Erythema marginatum: macular rash on trunk and extremities
Subcutaneous nodules
Fever
Elevated ASO ( Anti streptolysin O)
Elevated ESR ( Erythrocyte Sedimentation Rate)
Elevated CRP ( C- Reactive Protein)
Management:
Assess vital signs
Control joint pain and inflammation with massage
Febrile phase – provide bed rest
Limit physical exercise in child with carditis
Administer antibiotics (penicillin) as prescribed
Administer salicylates and anti-inflammatory agents
Instruct parents about the importance of follow up and need for antibiotic prophylaxis for
dental work, infection, invasive procedures
Advise child to inform the parents if anyone in school develops a strep throat infection
Assessment:
fever
conjunctival injection
red, cracked lips; “strawberry tongue”
Swollen hands, rash, enlargement of the cervical lymph nodes
Implementation:
monitor temperature frequently
assess heart sounds and rhythm
assess extremities for edema, redness, desquamation
monitor mucus membrane for inflammation
weigh daily
administer IV immune globulin
instruct parents in the administration of prescribed meds
aspirin – need to monitor bleeding
D. HEMATOLOGIC DISORDERS
(a) LEUKEMIA
the most frequent type of childhood cancer
Brain tumors – 2nd
Etiology:
Environmental - Viruses
Familial/genetic
Host factors
STAGES OF TREATMENT
1. INDUCTION
Goal: to remove bulk of tumor
Methods: surgery, radiotherapy, chemotherapy, BM transplant
Effects: often the most intensive phase
Side Effects potentially life threatening
2. CONSOLIDATION
Goal: to eliminated any remaining malignant cells
Methods: chemo/radio
Side effects will still be evident
3. MAINTENANCE
Goal: to keep the child disease free
Chemotherapy
This phase may last several years
4. OBSERVATION
Goal: to monitor the child at intervals for evidence of recurrent
disease and complications of treatment
Method: treatment is complete
Child may continue in this stage indefinitely
NURSING INTERVENTION
Help child cope with intrusive procedures
Provide information geared to developmental level and Emotional readiness
Explain what is going to happen, why it is necessary, how it will feel
Allow child to handle to handle and manipulate equipments
Allow child some control in situations
Positioning, selecting injection site
Support child and parents
Maintain frequent clinical conferences to keep all informed
Always tell the truth
Acknowledge feelings and encourage child/family to express them
Provide contact with another parent or support group
Minimize side effects of treatment
A. Skin breakdown
Keep clean and dry; wash with warm water; no soaps or creams
Do not wash off radiation marks
Avoid all topical agents with alcohol
Do not use heating pads or hot water bottle
B. Bone marrow suppression
Provide frequent rest periods
Avoid crowds
Evaluate any potential site of infection
Monitor temperature
Avoid use of aspirin
Select activities that are physically safe
C. Nausea and vomiting
Administer antiemetic at least half an hour before chemotherapy
Eat light meal prior to administration of therapy
Administer IVF if needed
D. Alopecia
Reduce trauma of hair loss
Buy wig before hair falls out
Discuss various head coverings
Avoid exposing head to sunlight
E. Nutrition deficits
Establish baseline
Provide high calorie, high protein
F. Developmental delay
Facilitate return to school as soon as possible
Discuss limit setting, discipline
LEUKEMIA
Most common form of childhood cancer
Peak 3-5 years
Proliferation of abnormal wbc that do not mature beyond the blast phase
Blast cells – infiltrate other organs – liver, spleen, lymph tissue
Types:
Acute Lymphocytic leukemia (ALL)
80-85%
Acute
75% chance of surviving
3. Aplastic crisis
Caused by the diminished production and increased destruction of RBCs, triggered by viral
infection or the depletion of folic acid
Profound anemia and pallor
Implementation:
Administer oxygen and blood transfusions
Administer analgesics
Maintain adequate hydration and blood flow with IV normal saline as prescribed and with
oral fluids
Assist the child to assume a comfortable position so that the child keeps the extremities
extended to bed no more than 30 degrees
Avoid putting strain on painful joints
Encourage consumption of a high calorie, high protein diet with folic acid supplementation
Administer antibiotics as prescribed
Monitor for signs of increasing anemia and shock (pallor, vital sign changes)
Implementation:
Blood transfusion
corticosteroids and immunosuppresives
splenectomy
bone marrow transplant
Medic Alert bracelet
(e) HEMOPHILIA
x linked recessive trait
Hemophilia A – deficiency of Factor VIII
Hemophilia B – deficiency of factor IX
Males inherit hemophilia from their mothers and females inherit the carrier status from
their fathers
Assessment:
prolonged bleeding after minor injury
At birth after cutting cord
Following circumcision
Following IM immunization
Increase bruising as child learns to crawl and walk
Abnormal bleeding in response to trauma
Joint bleeding – pain, tenderness, swelling limited range of motion
Tendency to bruise easily
Prolonged PTT
Normal BT, PT, platelet count
Implementation:
prepare to administer Factor VIII concentrate /cryoprecipitate
Thaw slowly
Gently rotate bottle
Infuse immediately; deteriorates at room temperature
monitor for bleeding
monitor for joint pain; immobilize the affected extremity if joint pain
occurs
assess neurological status ( child at risk for intracranial bleeding)
monitor urine for hematuria
Control bleeding by immobilization, elevation, application of ice; apply
pressure (15 mins) for superficial bleeding
instruct parents regarding activities of the child
avoidance of contact sports
E. GASTROINTESTINAL DISORDERS
(a) CLEFT LIP AND CLEFT PALATE
1 in 1000 births
multifactorial
common among children with chromosomal abnormalities
results from failure of the embryonic structures of the face to unite
may occur separately or may combine to produce a single unilateral or bilateral cleft from the lip
through the soft palate
interfere with the child’s capacity to meet oxygenation and nutritional needs
may seriously hamper normal bonding process of children with parents
Assessment:
facial abnormality visible at birth
cleft lip or palate or both, unilateral or bilateral
difficulty sucking
inability to form airtight seal around nipple
formula/milk escapes through nose in infants with cleft palate
predispose to infection – communication between mouth and nose
difficulty swallowing
abdominal distension related to excessive insertion of air
Management:
team approach : otolaryngologist, audiologist, pediatrician, dentist, orthodontist, speech
therapist
Surgical correction:
early correction – prevent speech defects (cleft palate)
CHEILOPLASTY
Correction of cleft lip
Unite edges to allow lips to be both functional; aesthetic reasons
Performed usually at age 2 ½ months
NURSING INTERVENTION:
Cleft Lip (PreOP)
feed in upright position
burp frequently
press cleft lip together with fingers – to encourage sucking and to strengthen muscles
if unable to suck, use a rubber tipped syringe; drip onto side of mouth
finish feeding with water to wash away formula in palate area
provide small, frequent feedings
provide emotional support for parents
Nursing Intervention:
Pre-Op cleft palate repair
prepare parents to care fro child after surgery
instruct concerning feeding methods and positioning
Post-Op cleft palate repair
position on side for drainage of blood
have suction available
prevent injury or trauma on suture line
Use cups only for liquids; no bottles
avoid straws, utensils, popsicle sticks, chewing gum
provide soft toys
Use elbow and wrist restraints
Provide liquid diet initially then soft diet
Give water after each feeding to clean suture line
Hold and cuddle
ESOPHAGEAL ATRESIA
congenital defect; upper segment of the esophagus ends in a blind pouch
TRACHEOESOPHAGEAL FISTULA
defect in which embryonic structures fail to divide into a separate esophagus and
trachea
opening between two structures
usually occur together
Assessment:
copious oral and nasal secretions –first sign of a defect
choke or cough
when suctioning or gavage is attempted – catheter cannot pass into
stomach
Medical and Surgical intervention
prevention of aspiration
drainage tube may be placed in the blind pouch –
to suction secretions
esophageal atresia – medical emergency
(end to end anastomoses)
feeding tube maybe inserted into the stomach through
gastrostomy until repair heals
Nursing intervention:
Provide nutrition
Provide gastrostomy tube feeding until anastomosis site has healed
Start oral feedings when infant can swallow well
Promote respiratory function
Position properly
Assessment:
olive size mass or bulge
under right rib cage -BQ
vomiting – projectile; non
bilous
peristaltic waves during and
after feeding
failure to thrive
dehydration Increased Hct
diagnostic tests: Metabolic alkalosis
UGIS – narrowing of diameter Decreased serum Na, K, Cl
of pylorus
Nursing intervention:
Pre-Op:
Replace fluids and electrolytes
Prevent vomiting
Give thickened feedings
High Fowler’s
Place on right side after feeding
Minimize handling
Strict I and O monitoring, daily weights, urine sp gravity
Post Op
Advance diet as tolerated
Place on right side after feeding
Observe incision for signs of infection
Provide client teaching and discharge planning
(d) INTUSSUSCEPTION
telescoping of bowel into itself
ileocecal region
edema, necrosis of bowel, obstruction
most common at age 6 months
more in boys than in girls
associated with cystic fibrosis
Assessment:
piercing cry
sausage shape mass in the abdomen upon palpation - BQ
severe abdominal pain (pulls leg up)
vomiting of bile stained fluid
bloody mucus in stool
“currant jelly” stool - BQ
Management:
barium enema
surgery
Nursing intervention:
Enema as ordered
Mineral oil or isotonic saline
Do not use water or soap suds – water intoxication
Use volume appropriate to weight of child
o infants – 150-200ml
o children – 250-500 ml
Administer TPN as ordered
Provide low residue diet
provide client teaching and discharge teaching
Colostomy care
Nursing intervention:
keep operative site clean
observe infant for signs of hypovolemic shock and infection
if anoplasty heals – regular dilatation of anus to prevent stricture
after surgery – side lying or prone with hips elevated
Assessment:
chronic diarrhea
failure to thrive
Steatorrhea
Distended abdomen
Abdominal pain, irritability, listlessness, vomiting
Symptoms of ADEK deficiency
Diagnostic tests:
pancreatic enzymes
jejunal or duodenal biopsies
Management:
diet therapy
gluten free diet
TPN in children
Nursing Intervention:
gluten free diet (BROW – Barley, Rye, Oatmeal, Wheat)
supplemental fat soluble vitamins
client teaching
gluten free diet
importance of reading the label
avoidance of infection
adhering to diet even if symptoms are controlled
importance of long term follow up
(h) APPENDICITIS
Inflammation of the appendix
Ischemia, gangrene, rupture, peritonitis – if untreated
School age children – most common surgical procedure -BQ
Due to mechanical obstruction or anatomic defects
Assessment:
diffuse pain RLQ
nausea, vomiting
guarding of abdomen
rebound tenderness
decreased bowel sounds
fever
diagnostic tests:
Complete blood count (CBC) reveals increase WBC
elevated acetone in urine
Nursing Intervention:
antibiotics/ antipyretics as ordered
no enemas may cause rupture
no heating pads
routine preop care
Post op care:
semi-Fowler’s position
Monitor NGT
Monitor penrose drains
(i) PARASITISM
roundworms, pinworms
Assessment:
pinworms – anal itching, disturbed sleep
roundworms – colic , abdominal pain, lack of appetite, weight loss
Nursing intervention:
obtain stool culture
observe all excreta for worms
Scotch tape swab
Instruct parents to change clothing, bed linens, towels and launder in hot water
Instruct all family members to scrub hands and fingernails prior to eating and after using toilet
F. INTEGUMENTARY DISORDERS
(a) ECZEMA
atopic dermatitis - often the first sign of an allergic
predisposition in a child
usually manifests during infancy
Asssessment:
erythema, weeping vesicles that rupture and crusts
severe pruritus; scratching causes thickening and
darkening
dry skin, sometimes urticaria
Medical Intervention:
topical steroids
Antihistamines
coal tar preparation
colloid baths
diet therapy: elimination of offending food
Nursing Intervention:
avoid heat and prevent sweating
check materials in contact with child’s skin (sheets, lotions, soap
avoid frequent baths
avoid use of soap
provide lubricant immediately after bath
administer topical steroids as ordered
use cotton instead of wool
keep child’s nails short; use elbow or glove restraints if needed
apply wet saline or Burrow’s solution compresses
G. MUSCULOSKELETAL DISORDERS
CARE OF THE CHILD WITH A CAST
if cast is of plaster – will remain wet for at least 24 hrs
use only the flats of their hands to move children
casts must remain open to the air until dry
casted extremities are elevated to help blood return and reduce swelling
Initial chemical hardening reaction may cause a change in an infant’s body
Choose toys too big to fit down cast
Do not use baby powder near cast – medium for bacteria
Prepare for anticipated casting by having child help apply cast in a doll
Nursing Intervention:
perform exercises as ordered
provide cast care
child who is learning to walk must be prevented from trying to stand; apply restraints if
necessary
provide diversional activities
provide skin care
client teaching
(c) SCOLIOSIS
lateral curvature of the spine
most commonly in adolescent girls
familial pattern; associated with other nueromuscular condition
idiopathic majority
Assessment:
failure of curve to straighten when child bends forward with knees straight and arms hanging
down feet
uneven bra strap marks
uneven hips
uneven shoulders
asymmetry of rib cage
xray: reveals curvature
Management:
stretching exercises
Milwaukee brace – worn 23 hours/day for 3 years
plaster jacket vest
spinal fusion
Nursing Intervention:
teach/encourage exercise
provide care for the child with Milwaukee brace
Child wears brace 23 hours/day
Monitor pressure points
Promote positive body image with brace
Provide cast care
Assist with modifying clothing for immobilization devices
Adjust diet with decreased activity
Provide client teaching and discharge instructions
o Exercise
o Cast care
Correct body mechanics
Alternative education for long term hospitalization
Availability of community agencies
H. GENITO-URINARY DISORDERS
(b) HYPOSPADIAS
urethral opening located anywhere along the ventral surface of penis
Assessment:
Urinary meatus misplaced
Inability to make straight stream of urine
Management:
minimal defects – no intervention
neonatal circumcision delayed, tissue maybe needed for corrective repair
surgery at age 3-9 months
Nursing Intervention:
diaper normally
provide support for parents
post op: check pressure dressing
monitor catheter drainage
(c) PHIMOSIS
an abnormal narrowing of the foreskin so that it cannot be retracted over the glans penis
may be present at birth or may develop as a result of poor hygiene with accumulation of smegma
Management:
Prevention – regular pulling the foreskin back and cleaning
Circumcision
Nursing intervention:
circumcision care
Close observation for bleeding
Ice application
Administration of analgesics
(d) ENURESIS
involuntary passage of urine after the age of control is expected (4 years)
Types:
A. Primary :in children who have never achieved control
B. Secondary: in children who have developed complete control
May occur anytime but most frequent at night
More common in boys
No organic cause
Etiologic possibilities:
Sleep disturbances
Delayed neurologic development
Immature development of bladder
Psychologic problems
Assessment:
PE normal
History of repeated voluntary urination management:
bladder retention exercises
Drug therapy
TCA – imipramine
Anticholinergics
Nursing Intervention:
Provide information/counseling to family:
Confirm that this not conscious behavior and that the child is not purposely misbehaving
Assure parents that they are not responsible and that this is a relatively common problem
Involve child in care; give praises and support with small accomplishments
Age 5-6 years – can strip wet beddings
Age 10-12 years – can do laundry and change bed
Avoid scolding and belittling the child
Assessment:
Associated structural changes
Prolapsed rectum
Inguinal hernia
Widely split symphysis
Rotated hips
Associated anomalies
Epispadias
Cleft scrotum or clitoris
Undescended testes
Chordee (downward deflection of the penis)
Management:
reconstructive surgery
urinary diversion
delayed until 3-6 months
Nursing intervention: Preop:
Provide bladder care; prevent infection
Keep area as clean as possible
Change diaper frequently; keep loose fitting
Wash with mild soap and water
Cover exposed bladder with vaseline gauze
Postop:
Design play activities to foster toddler’s need for autonomy
child will be immobilized for extended period of time
Prevent trauma; as child gets older and more mobile, trauma is more likely
Assessment:
Proteinuria
Hypoproteinemia
Hyperlipidemia
Dependent edema
Puffiness around the eyes in morning
Ascites
Scrotal edema
Ankle edema
anorexia, vomiting, diarrhea
Pallor, lethargy
Hepatomegaly
Management:
Drug therapy
Corticosteroids
Antibiotics
*diuretics are not given because it can lead to hypotension
Nursing Intervention:
Provide bed rest to conserve energy
Find activities for quiet play
Provide high protein, low sodium diet – during edema phase
Maintain skin integrity
Avoid IM injections – meds not absorbed in edematous tissues
Obtain morning urine for protein studies
Provide scrotal support
Monitor I and O, vital signs
Weigh daily
Administer medications as ordered
Protect from sources of infection
Assessment:
History of strep infection (URTI or impetigo)
Edema, anorexia, lethargy
Hematuria or dark colored urine
Fever
Hypertension
Diagnostic tests:
Urinalysis – RBC, WBC, protein, cellular casts
Urine specific gravity increased
BUN, creatinine increased
ESR elevated
Hgb, Hct decreased
Management:
Antibiotics for prophylaxis
Antihypertensives
Digitalis – if with CHF
Fluid restriction
Peritoneal dialysis – if severe renal complication occurs
Nursing Management:
Monitor I and O, BP
Weigh daily
Provide diversional activity
Provide client teaching and discharge planning
Medication administration
Prevention of infection
Signs of renal complications
Importance of long term follow up
J. NEURO-SENSORY DISORDERS
CRANIAL DEFECTS:
(a) CRANIOSYNOSTOSIS
one or more of the sutures close too soon
ICP increases; interferes with normal brain growth that may lead to mental retardation
Assessment:
Suture lines of the skull manually palpated
Radiographs are made to confirm
(b) MICROCEPHALY
The brain fails to grow
May be due to a chromosomal defect or from drugs, toxins or radiation
Mental Retardation (MR)
(c) HYDROCEPHALUS
Imbalance of CSF absorption or production
Caused by malformations, tumors, hemorrhage, infection, trauma
Types:
Communicating – impaired absorption within subarachnoid space
Non-communicating – obstruction of CSF flow within theventricular system
Assessment:
Infant – increased head circumference
Macewen’s sign – cracked-pot sound on percussion of bones of head
Anterior fontanel tense, bulging
Scalp veins dilated
Frontal bossing, sunsetting eyes
Child – behavior changes
Headache, nausea and vomiting
Ataxia, nystagmus
Surgical Implementation:
Goal: to prevent further CSF accumulation by bypassing the blockage and draining the fluid from
the ventricles to a location where it may be reabsorbed
VP Shunt – CSF drains into the peritoneal cavity from the lateral ventricle
AV Shunt – CSF drains into the right atrium
PostOP Care:
Keep child flat as prescribed – to avoid rapid reduction of intracranial fluid
Observe increase ICP – if present, elevate head of the bed no more than 30-45
Monitor for infection
Measure head circumference
Monitor I and O
Provide comfort measures; administer medications (diuretics, antibiotics, or
anticonvulsants)
Toddler – headache and anorexia is the earliest common signs of shunt malfunction
Implementation:
Evaluate sac; measure lesion
Neuro check frequently
Monitor for increase ICP
Measure head circumference; assess fontanels (if
still open)
Protect the sac
Cover with sterile, moist (normal saline) non-adherent dressing
Change dressing every 2-4 hours or as needed
Place prone position
Head is turned to one side for feeding
Diapering may be C/I until defect repaired
Always obsrve aseptic technique when providing care
Watch for early signs of infection
Administer antibiotics as prescribed
Administer anticholinergics – improve urinary continence
Administer laxatives and antispasmodics as prescribed
(e) MENINGITIS
infectious process of the CNS caused by bacteria and viruses
acquired as a primary or as a result of complications
diagnosis – CSF analysis (increase pressure, cloudy CSF, high protein, low glucose)
bacterial or viral
Assessment:
signs and symptoms vary depending of age group
fever, chills
vomiting, diarrhea
poor feeding or anorexia
altered LOC
bulging anterior fontanel
nuchal rigidity
Implementation:
RESPIRATORY ISOLATION; maintain for at least 24 hours after antibiotics are initiated
administer antibiotics as prescribed
monitor VS and neuro status
Monitor I and O
assess nutritional status
determine close contacts of the child with meningitis
Assessment:
extreme irritability and crying
feeding difficulties
stiff and rigid arms and legs
delayed gross development
abnormal motor performance
alterations of muscle tone
abnormal posturing
persistence of primitive reflexes
Implementation:
early recognition
PT, OT, speech therapy, education and recreation
assess the child’s developmental level and intelligence
early intervention
encourage communication and interaction with the child on a functional level
provide safe environment
position upright after meals
provide safe, appropriate toys for age and developmental level