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Di s e a s e s o f t h e
             Ne wb o r n
 Pr e p a r e d b y : Ha n s Ch r i s t i a n f . Vi t u g RN,
                                                             MA N c
 F a c u l t y /C l i n i c a l I n s t r u c t o r /R e v i e w e r
"Necrotizing"
means the death
of tissue, "entero"
refers to the
small intestine,
"colo" to the large
intestine, and
"itis" means
inflammation.
An acute
inflammatory
disease of the bowel
with increased
incidence in
preterm and high
risk infants
Theories to Support that Explains NEC
1.Little supply of oxygenation -> plus feeding ->
 stress to the intestinal wall -> allowing bacteria
 to invade intestinal wall and bloodstream ->
 necrosis/perforation of the intestinal wall ->
 decrease absorption of the vitamins and
 minerals and Leak of bacteria into abdomen
 causing peritonitis.

2.Difficult deliveries -> deprived oxygenation ->
 vital organs receives more oxygen

3.Increased RBC counts – thickens the blood
 and impaired circulation -> hinder the
 transport of oxgenation
How does it happen?
• Prematurity remains the most prominent risk
  factor

• Great damage to mucosal lining  diminished
  blood supply  stop secreting protective
  lubricating mucus  unprotected bowel attacked
  by proteolytic enzymes  unable to synthesize
  IgM  Gas-forming bacteria invades damaged
  area  produce intestinal pneumatosis (presence
  of air in the submucosal or subserosal surfaces of
  the bowel)
Signs and Symptoms
•   Infant may “not look well”
•   Poor feeding
•   Apnea
•   Vomiting (often bile stained)
•   Decreased U/O
•   Hypothermia
•   Distended abdomen
•   Gastric residuals
•   Blood in the stools
Diagnostic Evaluation

Radiography
Sausage-shaped
dilation of the
intestines
“Soap suds” or
bubbly appearance o
f thickened bowel
wall
Diagnostic Evaluation
Laboratory
examinations
  – Anemia
  – Leukopenia
  – Leukocytosis
  – Metabolic acidosis
  – Electrolyte
    imbalance
Therapeutic Management
• Oral feedings withheld
  for at least 24 to 48
  hours
• Breast feeding is
  preferred
• Antibiotics
• Probiotics
  – Lactobacillus acidophilus
  – Bifidobacterium infantis
Nursing Management
• Observation and assessment
• Infants left undiapered
• Position infant supine or on the
  side
• Vital signs including blood
  pressure
  –Avoid rectal temperature
TRANSIENT TACHYPNEA OF THE NEWBORN
Some newborns' breathing during
the first hours of life is more rapid
and labored than normal because
of a lung condition called transient
tachypnea of the newborn (TTN).
Definition
• A respiratory problem seen in the newborn
  shortly after delivery
• It is likely due to retained lung fluid
• Common in 35+ week gestation babies who are
  delivered by caesarian section without labor
• Resolves over 24-48 hours
• Causative Factors
  – Pulmonary immaturity
  – Mild surfactant deficiency
Causes of TTN
TTN, also called "wet lungs" or type II
respiratory distress syndrome, usually
can be diagnosed in the hours after
birth.

TTN can occur in both preemies
(because their lungs are not yet fully
developed) and full-term babies.
New borns at higher risk for TTN
include those who are:

delivered by cesarean section
(C-section)
born to mothers with diabetes
born to mothers with asthma
small for gestational age (small
at birth)
Pathophysiology
• Lower levels of circulating catecholamines
  after a caesarean section which are
  necessary to alter the function of channels
  that absorb excess fluid from the lungs
• Delayed absorption of fetal lung fluid from
  the pulmonary lymphatic system
  increased fluid in the lungs  increased
  airway resistance and reduced lung
  compliance
Clinical Manifestations
• Period of rapid breathing
• Tachypnea
• Intracostal and subcostal
  retractions
• Grunting
• Nasal flaring
• Possible cyanosis
Diagnostic Evaluation and Therapeutic
            Management
• Diagnostic evaluation
  – Chest X-ray
  – Levels of PG were found to be negative in
    certain newborns


• Management
  – Supplemental oxygen
  – Antibiotics
ERYTHROBLASTOSIS FETALIS/HEMOLYTIC DISEASE OF THE
                   NEWBORN
Abnormal, rapid
destruction of RBC
Hyperbilirubinemia
in the first 24
hours of life is
most often the
result
Hemolytic disease of the newborn (HDN)
Major causes of RBC destruction
  – Rh Incompatibility (Isoimmunization)
     • Mother is Rh negative, and infant is Rh positive
     • May not occur in first pregnancy
     • Increased risk of fetal blood being transferred to
       maternal circulation  subsequent pregnancy with
       Rh (+) fetus maternal antibodies formed will attach
       and destroy fetal erythrocytes
     • Progressive hemolysis in utero  fetus
       compensates, accelerates rate of erythropoesis 
       immature RBCs appear  erythroblastosis fetalis
       (hydrops fetalis)
Hemolytic disease of the newborn (HDN)
Major causes of RBC destruction
  – ABO Incompatibility
    • Between a mother with type O and an infant
      with A or B blood groups.
    • Anti-A and Anti-B already present in the
      maternal circulation cross the placenta and
      attach to fetal RBCs  hemolysis
    • Less severe hemolytic reaction the Rh
      incompatibility
    • May occur in first pregnancy
Signs and Symptoms
Jaundice
  –Most not
   jaundice at
   birth
Anemia
Hypovolemic
shock may develop
Hypoglycemia
Diagnostic Evaluation

• Maternal antibody titer
  (Indirect Coomb’s test)
• Amniocentesis
• Ultrasound
Therapeutic Management
Prevention of Rh Isoimmunization
  –Administration of RhIg
  –RhIg (RhoGAM) – must be administered
   to unsensitized mothers within 72 hours
   after the first delivery
  –Admin of RhIg at 26 to 28 weeks of
   gestation further reduces risk of
   isoimmunization
Therapeutic Management
• Exchange Transfusion
  –Infants blood is removed in small
   amounts (5 to 10 ml at a time) and
   replaced with compatible blood
  –For severe hydrops
• ABO incompatibility
  –Early detection and phototherapy
Nursing Management
• Recognizing jaundice – initial nursing
  responsibility
• Prepares family incase of transfusion and
  assist practitioner
  – Infant remains NPO during procedures
  – Maintain documentation of blood volume
    exchange, time, cumulative record of the total
    blood exchanged
  – Vital signs
  – Signs of transfusion reactions
DOWN SYNDROME
Down Syndrome
• The genetic disorder most frequently seen as
  causing moderate to severe mental
  retardation
• Etiology is unknown
  – Genetic predisposition
  – Exposure to radiation before conception
  – Immunologic problems
  – Infection
Clinical Manifestations
•   Bradycephaly
•   Back of the head is flat
•   Epicanthal folds
•   Palpebral fissure slanting
    laterally upward
•   Tongue may protrude
•   Narrow palate
•   Low-set ears
•   Short broad hands
•   Transpalmar crease (simian
    line)
•   Short stature
•   Rag-doll appearance
•   IQ of 50-70
Diagnostic Evaluation

• Evident at birth
• Prenatal testing
• Chromosomal
  analysis
Therapeutic Management

• Surgery to correct cardiac
  abnormalities, GI malformations
  and craniofacial deviations
• Neck radiography before the child
  participates in any sports
Nursing Management
• Options for fluid and calorie intake
  – Breastfeeding may not be possible, immature
    sucking reflex
  – Special bottles and utensils
• Routine
  – Changes causes frustration and decreased coping
    abilities
• Encourage self-care
• Advise X-rays before participating in sports
TEMPERATURE CONTROL
Cold Stress
• Infants lack shivering response
• Norepinephrine (SNS) stimulates fat metabolism
  to produce internal heat  blood  surface
  tissues
• Increased in metabolism  increased oxygen
  consumption
• Norepinephrine  vasoconstriction  decrease
  oxygen decreased glucose metabolism
• Results: Hypoxia, Metabolic acidosis,
  Hypoglycemia
Three primary methods for maintaining a
     neutral thermal environment

• Incubator
• Radiant warming
  panel
• Open bassinet
  with cotton
  blankets
Temperature control

• Warm items
  first
• Plastic wrap
• Careful drying
• Kangaroo care
Incubator Care
• Double walled incubators
 –improve infants ability to maintain a
  desirable temp reduces energy
  expenditure r/t heat regulation
• Pre-warm incubator first
• Head covering when outside of the
  incubator
Essential public strategy that enables
the early detection and management of
several congenital metabolic disorders,
which if left untreated , may lead to
mental retardation and even death

For early detection and management of
congenital metabolic disorders
THE NEWBORN SCREENING PROGRAM
Newborn Screening Program (NBS)

• Mandated through RA 9288 (The
  Newborn Screening Act of 2004)
• Done between 24-72 hours after
  birth
Collection of NBS Samples
• Through heel prick method: 4
  drops of blood is drawn from
  heel puncture blotted onto a
  filter paper
• Air dry 4-6 hours
• Sent to laboratory within 24
  hours
• BEST - 48th to 72nd hours of life
• ACCEPTABLE - anytime after 24
  hours from birth until 2 weeks
  of age
Sample collection done
before the ideal time may
result in:
 Falsely elevated thyroid stimulating
 hormone (TSH) = false (+) screen for
 CH
 Falsely elevated 17
 hydroxyprogesterone (17-OH-P) =
 false (+) screeen for CH
 Falsely low galactose and
 phenylalalnine = false (-) screen for
 GAL and PKU
Disorders tested for newborn screening

• Congenital Hypothyroidism (CH)
• Congenital Adrenal Hyperplasia
  (CAH)
• Galactosemia (GAL)
• Phenylketonuria (PKU)
• Glucose-6-Phospate-Dehydrogenase
  Deficiency (G6PD)
Congenital Hypothyroidism (CH)
Congenital Hypothyroidism (CH)

• aka Cretinism
• Lack or
  absence of
  thyroid
  hormone
(H-U-Mi-D)
Hereditary conditions
Underdevelopment of the fetal
thyroid glands

Maternal Intake of anti thyroid drugs
during pregancy

Deficiency, Maternal Iodine
*Manifestations
Poor suck and feeding
Jaundice
Hypotonia
Cool pale dry skin
Swelling around the eyes
Large swollen tongue
Large fontanels with late closure
Poor weight gain and growth
Hoare sounding cry
Delayed milestone (sitting, crawling, walking
and talking)
*Treatment
Lifetime oral doses of thyroid hormone. L-
Thyroxine

Nursing Considerations:
Instruct parents to avoid Soy-based
formulas and iron supplements.
Avoid adjusting medications without
MD’s order to prevent under
medication or over medication.
Excessive medication can
cause : D-I-T-S
Diarrhea
Inability to sleep
Tachycardia
Shakiness in the child
*Treatment
Regular
monitoring of
the child’s
weight, overall
health and
thyroid
hormones level
Congenital Adrenal Hyperplasia (CAH)
Congenital Adrenal Hyperplasia (CAH)

• Excessive or deficient production of
  sex steroids
• Severe salt loss, dehydration and
  abnormally high levels of male sex
  hormones in both boys and girls
• If not detected and treated early,
  infants may die within 7-14 days
Congenital Adrenal Hyperplasia (CAH)
CAH is caused by a
deficiency of adrenal
gland hormones.


21 hydroxylase
is missing or not
working correctly.
Congenital Adrenal Hyperplasia (CAH)
21-OH is responsible for the production
of hormones :
CORTISOL is involved in glucose
metabolism and in normal inflammation
and immune response.
ALDOSTERONE is responsible for blood
pressure and sodium retention.
Congenital Adrenal Hyperplasia (CAH)

*Manifestations
•   Poor feeding
•   Listlessness and drowsiness
•   Vomiting
•   Diarrhea
•   Weight loss
•   Hypotension
•   Hyponatremia
•   Metabolic acidosis
Muscle growth at an early age




Enlargement of penis during childhood
Early deepening of the
voice




Early beard
Pubic hair and underarm hair during
childhood




                    Severe acne
M-E-E-E-P-S-S
Muscle growth at an early age
Enlargement of penis during childhood
Early deepening of the voice
Early beard
Pubic hair and underarm hair during
childhood
Smaller than normal testicles
Severe acne



Male pattern baldness
Early puberty changes such as hair in
airmpits and pubic area




Lack of menstrual periods or scanty or
irregular periods
Excess hair on the face and body




Deep, husky voice
(S-M-E-L-E-D)
Severe acne
Male pattern baldness
Early puberty changes such as hair
in airmpits and pubic area
Lack of menstrual periods or scanty
or irregular periods
Excess hair on the face and body
Deep, husky voice
*Treatment
Lifetime administration of the
deficient or missing hormones
HYDROCORTISONES
lessens the amount of
androgens (prevents early
puberty and allows for more
typical growth and
Over medication can results to
Cushing’s syndrome (Stretch
marks, rounded face, weight
gain, hypertension and bone
loss).

Under medication can occur
during periods of stress and
illness when higher doses of the
Corrective
surgery for
enlarged clitoris
(can be done as
early as one to
three years of
age. To separate
labia and to
Galactosemia (GAL)
Galactosemia (GAL)

This hereditary disorder is
characterized by the lack of the
enzyme Galactose-1-Phosphate
uridyl Transferase (GALT) that
converts galactose to glucose, the
form of sugar that can be used by
body cells.
Galactosemia (GAL)
Initial symptoms also include: (F-L-I-P)

Failure to gain weight
Lethargy
Irritability
Poor feeding and poor suck
Galactosemia (GAL)

Treatment: Giving the child a special
lactose free formula and exclusion of
lactose and galactose foods such as
milk (including breast milk) and other
dairy products from the diet through
out life.
Galactosemia (GAL)

Foods that should be avoided:
Milk and all dairy products
Processed and pre packaged foods
Tomato sauces
Certain medications
Any foods or drugs which contain the ingredients
Lactulose, Casein, Caseinate, Lactalbumin, Curds,
Whey or Whey solids
Galactosemia (GAL)

Calcium and Vitamin D
deficiency is likely to develop
in a child on a lactose free.
Therefor, the child is given
supplements to prevent
deficiencies
Phenylketonuria (PKU)
Phenylketonuria (PKU)

A metabolic disorder characterized by
lack of enzyme Phenylalanine
hydroxylase (PAH) needed to process
the amino acid phenylalanine

The resultant build up of the said
protein in the body leads to mental
retardation
Phenylketonuria (PKU)
• Excessive accumulation of
  phenylalanine = brain
  damage
• Dx – Guthrie test
• Mx - Low protein diet;
  breastmilk
Glucose-6-Phospate-Dehydrogenase
        Deficiency (G6PD)
G6PD is one of
many enzymes
that help the
body process
carbohydrates
and turn them
into energy.
Glucose-6-Phospate-Dehydrogenase
        Deficiency (G6PD)
• A condition where the body lacks
  the enzyme called G6PD a
  metabolic enzyme especially
  important in RBC metabolism
• Hemolytic anemia resulting from
  exposure to certain drug, food
  and chemical
Child during Hospitalization
STRESSORS AND THE CHILD’S REACTION
Illness and Hospitalization:
Children are particularly vulnerable
to the crises of illness and
hospitalization because:

1.Stress represents a change from
 the usual state of health and
 environmental routine

1.Children have limited number of
 coping mechanisms to resolve
 stressors
SEPARATION ANXIETY
• Also known as Anaclitic depression
• Major stress especially for children
  ages 16 to 30 months
• Three Phases:
   –Phase of Protest
   –Phase of Despair
   –Phase of Detachment
SEPARATION ANXIETY
           Three Phases:
Phase of Protest
  • React
    aggressively to
    separation from
    parent
  • Behavior is from
    a few hours to
    several days
SEPARATION ANXIETY
           Three Phases:

Phase of
Despair
 •Child is less
  active
 •Withdraws
  from others
SEPARATION ANXIETY
             Three Phases:
Phase of
Detachment
 • Also called denial
 • Appears detached
   and uninterested in
   parents’ visits
 • Appears to finally
   adjust to the
   surroundings
Loss of Control
  INFANTS
  – Trust
  – Inconsistent care and deviations from daily routine
• TODDLERS
  –   Autonomy
  –   Egocentric pleasures
  –   Rely on the consistency and familiarity of daily rituals
  –   Altered routine and rituals
  –   Regression
• PRESCHOOLERS
  – Egocentrism and magical thinking
  – Physical restriction, altered routines and enforced dependency
Bodily Injury and Pain
• INFANTS
  – Infants younger than 6 months
     • no obvious memory of previous pain
  – Facial expression of discomfort
  – React with physical resistance
  – Distraction and anticipatory preparation does little to
    lessen immediate reaction to pain
• TODDLERS
  – Intrusive experience produce anxiety
  – React with intense emotional upset and physical resistance
  – Communicate about their pain
Bodily Injury and Pain
• PRESCHOOLERS
  – Cause of illness is seen as concrete action the child
    does or the child fails to do  self-blame
  – Contagion – proximity of two object or persons
    causes the illness
  – Injection - fear that the puncture will not close
• SCHOOL-AGE CHILDREN
  – May be less concerned with pain than disability
  – Major concern is their fear of being told that
    something is wrong with them
  – Aware of the significance of different illnesses
Bodily Injury and Pain
• SCHOOL-AGE CHILDREN
  – Passive acceptance of pain
  – Nondirective request for support
  – When someone identifies unspoken messages
    and offers support, they readily accept it
• ADOLESCENTS
  – The nature of bodily injury may be more
    important based on the adolescents’ perception
    rather than the actual degree of severity of the
    illness
  – Changes in body image is their concern
  – Privacy
  – Reluctance to disclose pain
NURSING CARE OF THE CHILD WHO IS
HOSPITALIZED
Communication
• Speak in quiet pleasant tones
• Bend down
• Do not use clichés.
• Explain all procedures
• Be honest
• Be careful in making promises
• Observe nonverbal communication for clues to level of
  understanding
• Do not threaten
• Allow child to show feelings
• Provide time to talk
Communication
• Teach parents to anticipate next stage of development
• If teaching is interrupted, start over from the beginning
• Provide independence
• Do not compare child’s progress to that of anyone else
• Provide praise
• Instead of asking what something is, ask child to give it
  a name or tell you about it
• Allow choices where possible
• Involve parents in child’s care
Communication
• Keep routines
• If parents cannot stay with child, encourage
  them to bring in a favorite toy, pictures of
  family members or to make tape to played for
  the child
Play
• Toddler
   – Enjoys repetition
   – Solitary play
   – Parallel play

• Preschooler
   – Role play, make believe, associative play

• School-age
   – Group, organized activities
   – Group goals with interaction
Play
• Play is a very important part of development for your
  growing child.

• Not only is play time entertaining for your child, but it
  also provides stimulation, increases skills and
  coordination, provides an outlet for your child's
  energy, and helps to encourage exploration by your
  child.
Play is also important for the following
        reasons (Lippincott Williams & Wilkins, 2005)
Play is an excellent
stress reducer and
tension reliever. It
allows the child
freedom of
expression to act out
his fears, concerns
and anxieties
Play is also important for the following
       reasons (Lippincott Williams & Wilkins, 2005)

Play provides a
source of
diversional
activity,
alleviating
separation
anxiety
Play is also important for the following
        reasons (Lippincott Williams & Wilkins, 2005)
Play provides the
child with a sense of
safety and security
because while he is
engaging in play, he
knows that no
painful procedures
will occur.
Play is also important for the following
        reasons (Lippincott Williams & Wilkins, 2005)
Developmentally
appropriate play fosters
the child’s normal
growth and
development, especially
for children who are
repeatedly hospitalized
for chronic conditions
Play is also important for the following
        reasons (Lippincott Williams & Wilkins, 2005)
• Play puts the
  child in the
  driver’s seat,
  allowing him to
  make choices
  and giving him a
  sense of control
Play
  – Way to solve problems
  – Express creativity
  – Decrease stress
  – Prepare for procedures
  – Enhance fine and motor skills
• Make play appropriate for mental age and
  physical/disease state
• Multisensory stimulation
• Safe toys for mental age
• Offer play specific to age group
NURSING CARE OF THE CHILD IN PAIN
Concept of Pain
Preoperational Thought (2-7 yrs)
Relates to pain primarily as physical concrete experience
Magical disappearance of pain
Pain as punishment
Hold someone accountable for own pain
Concrete Operational Thought (7-10 yrs)
Relates to pain physically
Perceive psychologic pain
Fears bodily harm & annihilation
Pain as punishment
Formal Operational Thought (13 yrs and older)
Give reason for pain
Perceives several types of psychologic pain
Fears losing control during painful experience
Q-U-E-S-T (PAIN ASSESSMENT)

QUESTION the child’s parents and child
too, if he is old enough to respond
USE appropriate pain assessment
EVALUATE the child’s behaviour
SECURE the parent’s active participation
in treatment
TAKE the cause of the pain into
consideration
ASSESSMENT
• Wong-Baker FACES Pain Rating Scale
ASSESSMENT
• FLACC (Face, Legs, Activity, Cry and
  Consolability) – for infants and very
  young children

• Behavior is observed to assess pain
Measures each of the five identified
categories on a 0 to 2 scale
• The higher the total score, the more pain
CRIES Neonatal Postoperative Pain
           Measurement Scale

Crying
Requires oxygen to maintain saturation
about 95%
Increased heart rate and blood
pressure
Expression
Sleeplessness
Neonatal Infant Pain Scale

Facial Expression
Crying
Breathing
patterns
State of arousal
Movement of
arms and legs
Premature Infant pain Profile

Gestational age
Heart rate
Oxygen saturation
Behavioral state
Brow bulge
Eye squeeze
Nasolabial furrow
INFANT               Mouth stretched open

                     Eyes tightly shut
Facial expression


                    Brows and forehead
                    knitted

                    Cheeks raised high enough
Younger Children
 Narrowing of the eyes
 Grimace or fearful appearance
 Frequent and longer lasting bouts of
 crying with a tone that is higher and
 louder than normal
 Less receptiveness to comforting by
 parents or other caregivers
 Holding or protecting the painful
 areas
P-A-I-N Management

Pharmacologic interventions
Anticipate and prevent or minimize pain
related to hospitalization, procedure and
treatment

Identify and relieve existing pain
Non pharmacologic interventions to reduce
stress, increase comfort and enhance
Pharmacologic Intervention – mainstay of pain
management and it depends on the specific
needs of the patient

Opioid analgesics
-Highly effective pain relievers and
constitute the core of most pharmacologic
interventions to manage acute pain in
infants and children
-Oral, sublingual, rectal, nasal,
subcutaneous, transdermal, IV and
intraspinal
*Morphine (MS contin)
*Fetanyl (Duragesic)
Non Opioid Analgesics
-are prescribed to manage
mild to moderate pain.
-infants and children
metabolize non opioid
analgesics in the same manner
and at the same rate as adult.
NSAIDS
-relieve for mild to moderate pain and
anti inflammatory effects
-Ibuprofen (advil); Naproxen
(Naprosyn); Tolmetin (Tolectin);
Indomethacin (Indocin) & Ketorolac
(Toradol) are approved for use in
children
-S.E: Inhibition of platelet aggregation
and GI irritation
Acetaminophen
-Is the DOC for treating mild pain.
Available in suppository, liquid and table
form.

-it has the added benefit of helping
reduce fever and is very safe, even for
neonates.

-long term can cause risk of liver
damage
EMLA Cream (lidocaine 2.5% and
          prilocaine 2.5%),
applied to intact skin
under occlusive
dressing, provides
dermal analgesia by
the release of
lidocaine and
prilocaine from the
cream into the
epidermal and dermal
layers of the skin
• Complementary and alternative medicine (CAM)
   – Complementary Pain Medicine
     •   Music Therapy
     •   Hypnosis
     •   TENS (transcutaneous electric nerve stimulation) unit
     •   Acupuncture
  – Non-Pharmacologic Care
     •   Comfort, positioning and non-nutritive sucking
     •   Distraction
     •   Relaxation
     •   Guided Imagery
     •   Biofeedback
     •   Behavioral Contracting
Pediatric Surgery
Pediatric Surgery
• Preoperative classes
    – Younger – simple and as close to the time of the
      procedure as possible
•   Allow to play with equipment
•   Teach and provide time to practice
•   Show pictures
•   Describe sensations
•   Detect misconceptions or fantasies
•   Parents can often be helpful in preparing
PEDIATRIC SURGERY
• Preoperative class
• Listen to child for clarifying misunderstandings
• Give simple information about the system that
  will be affected
• Use of anatomically correct dolls
• Preschool boys: allow to look at penis after
  surgery
• Post surgery: helping child master a threatening
  situation and minimizing physical and
  psychological complications
CHRONICALLY ILL PEDIATRIC CLIENTS:
CONCEPTS OF DEATH DYING AND GRIEVING
Concept of Death in Childhood
   (Lippincotts William and Wilkins, 2005)

Infancy
Concept of death – NONE
Nursing considerations:
Be aware that the older infant
will experience separation
anxiety
Help the family cope with death
so they can be available to the
infant
Concept of Death in Childhood
    (Lippincotts William and Wilkins, 2005)

Early childhood
Knows the words “DEAD” and
“DEATH”. Reactions are influenced
by the attitude of the parents.
Nursing considerations:
Help the family members including
siblings cope with their feelings
Allow the child to express his own
feelings in an open and honest
manner.
Concept of Death in Childhood
    (Lippincotts William and Wilkins, 2005)

Middle childhood.
Understands universality and
irreversibility of death. May have
a fear of parents dying.
Nursing considerations
Use play to facilitate the child’s
understanding of death
Allow siblings to express their
feelings.
Concept of Death in Childhood
    (Lippincotts William and Wilkins, 2005)

Late childhood
Beings to incorporate family and cultural beliefs
about death. Explores views of an afterlife and
faces the reality of own mortality
Nursing considerations
Provide opportunities for the child to verbalize his
fears
Help the child discuss his concerns with the family
Concept of Death in Childhood
    (Lippincotts William and Wilkins, 2005)

Adolescence
Adult perception of death, but still focused on the
HERE and NOW
Nursing considerations
Use opportunities to open discussion about death
Allow expression of feelings of guilt, confusion and
anxiety
Support and maintain self esteem
Helping Families to Cope

• Accept and support participants
• Be available and express your availability
• Encourage parents to assist in the care of
  their child
• Encourage involvement of siblings
• Religious associations as source of
  strength and support
Helping parents to talk with their child about dying
if he is ready to do so
Encouraging all family members to express their
feelings, even though they might be difficult to
hear
Allowing families to spend as much time as
possible with the dying child
Allowing and encouraging parents to continue to
take an active role in their child’s care
Reminding parents that they don’t always have to
be strong and ask for help
Thank you for Listening!

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2 diseases of the newborn

  • 1. Di s e a s e s o f t h e Ne wb o r n Pr e p a r e d b y : Ha n s Ch r i s t i a n f . Vi t u g RN, MA N c F a c u l t y /C l i n i c a l I n s t r u c t o r /R e v i e w e r
  • 2. "Necrotizing" means the death of tissue, "entero" refers to the small intestine, "colo" to the large intestine, and "itis" means inflammation.
  • 3. An acute inflammatory disease of the bowel with increased incidence in preterm and high risk infants
  • 4. Theories to Support that Explains NEC 1.Little supply of oxygenation -> plus feeding -> stress to the intestinal wall -> allowing bacteria to invade intestinal wall and bloodstream -> necrosis/perforation of the intestinal wall -> decrease absorption of the vitamins and minerals and Leak of bacteria into abdomen causing peritonitis. 2.Difficult deliveries -> deprived oxygenation -> vital organs receives more oxygen 3.Increased RBC counts – thickens the blood and impaired circulation -> hinder the transport of oxgenation
  • 5. How does it happen? • Prematurity remains the most prominent risk factor • Great damage to mucosal lining  diminished blood supply  stop secreting protective lubricating mucus  unprotected bowel attacked by proteolytic enzymes  unable to synthesize IgM  Gas-forming bacteria invades damaged area  produce intestinal pneumatosis (presence of air in the submucosal or subserosal surfaces of the bowel)
  • 6. Signs and Symptoms • Infant may “not look well” • Poor feeding • Apnea • Vomiting (often bile stained) • Decreased U/O • Hypothermia • Distended abdomen • Gastric residuals • Blood in the stools
  • 7. Diagnostic Evaluation Radiography Sausage-shaped dilation of the intestines “Soap suds” or bubbly appearance o f thickened bowel wall
  • 8. Diagnostic Evaluation Laboratory examinations – Anemia – Leukopenia – Leukocytosis – Metabolic acidosis – Electrolyte imbalance
  • 9. Therapeutic Management • Oral feedings withheld for at least 24 to 48 hours • Breast feeding is preferred • Antibiotics • Probiotics – Lactobacillus acidophilus – Bifidobacterium infantis
  • 10. Nursing Management • Observation and assessment • Infants left undiapered • Position infant supine or on the side • Vital signs including blood pressure –Avoid rectal temperature
  • 11. TRANSIENT TACHYPNEA OF THE NEWBORN
  • 12. Some newborns' breathing during the first hours of life is more rapid and labored than normal because of a lung condition called transient tachypnea of the newborn (TTN).
  • 13. Definition • A respiratory problem seen in the newborn shortly after delivery • It is likely due to retained lung fluid • Common in 35+ week gestation babies who are delivered by caesarian section without labor • Resolves over 24-48 hours • Causative Factors – Pulmonary immaturity – Mild surfactant deficiency
  • 14. Causes of TTN TTN, also called "wet lungs" or type II respiratory distress syndrome, usually can be diagnosed in the hours after birth. TTN can occur in both preemies (because their lungs are not yet fully developed) and full-term babies.
  • 15. New borns at higher risk for TTN include those who are: delivered by cesarean section (C-section) born to mothers with diabetes born to mothers with asthma small for gestational age (small at birth)
  • 16. Pathophysiology • Lower levels of circulating catecholamines after a caesarean section which are necessary to alter the function of channels that absorb excess fluid from the lungs • Delayed absorption of fetal lung fluid from the pulmonary lymphatic system increased fluid in the lungs  increased airway resistance and reduced lung compliance
  • 17. Clinical Manifestations • Period of rapid breathing • Tachypnea • Intracostal and subcostal retractions • Grunting • Nasal flaring • Possible cyanosis
  • 18. Diagnostic Evaluation and Therapeutic Management • Diagnostic evaluation – Chest X-ray – Levels of PG were found to be negative in certain newborns • Management – Supplemental oxygen – Antibiotics
  • 19. ERYTHROBLASTOSIS FETALIS/HEMOLYTIC DISEASE OF THE NEWBORN Abnormal, rapid destruction of RBC Hyperbilirubinemia in the first 24 hours of life is most often the result
  • 20.
  • 21. Hemolytic disease of the newborn (HDN) Major causes of RBC destruction – Rh Incompatibility (Isoimmunization) • Mother is Rh negative, and infant is Rh positive • May not occur in first pregnancy • Increased risk of fetal blood being transferred to maternal circulation  subsequent pregnancy with Rh (+) fetus maternal antibodies formed will attach and destroy fetal erythrocytes • Progressive hemolysis in utero  fetus compensates, accelerates rate of erythropoesis  immature RBCs appear  erythroblastosis fetalis (hydrops fetalis)
  • 22. Hemolytic disease of the newborn (HDN) Major causes of RBC destruction – ABO Incompatibility • Between a mother with type O and an infant with A or B blood groups. • Anti-A and Anti-B already present in the maternal circulation cross the placenta and attach to fetal RBCs  hemolysis • Less severe hemolytic reaction the Rh incompatibility • May occur in first pregnancy
  • 23. Signs and Symptoms Jaundice –Most not jaundice at birth Anemia Hypovolemic shock may develop Hypoglycemia
  • 24. Diagnostic Evaluation • Maternal antibody titer (Indirect Coomb’s test) • Amniocentesis • Ultrasound
  • 25. Therapeutic Management Prevention of Rh Isoimmunization –Administration of RhIg –RhIg (RhoGAM) – must be administered to unsensitized mothers within 72 hours after the first delivery –Admin of RhIg at 26 to 28 weeks of gestation further reduces risk of isoimmunization
  • 26. Therapeutic Management • Exchange Transfusion –Infants blood is removed in small amounts (5 to 10 ml at a time) and replaced with compatible blood –For severe hydrops • ABO incompatibility –Early detection and phototherapy
  • 27. Nursing Management • Recognizing jaundice – initial nursing responsibility • Prepares family incase of transfusion and assist practitioner – Infant remains NPO during procedures – Maintain documentation of blood volume exchange, time, cumulative record of the total blood exchanged – Vital signs – Signs of transfusion reactions
  • 29. Down Syndrome • The genetic disorder most frequently seen as causing moderate to severe mental retardation • Etiology is unknown – Genetic predisposition – Exposure to radiation before conception – Immunologic problems – Infection
  • 30. Clinical Manifestations • Bradycephaly • Back of the head is flat • Epicanthal folds • Palpebral fissure slanting laterally upward • Tongue may protrude • Narrow palate • Low-set ears • Short broad hands • Transpalmar crease (simian line) • Short stature • Rag-doll appearance • IQ of 50-70
  • 31. Diagnostic Evaluation • Evident at birth • Prenatal testing • Chromosomal analysis
  • 32. Therapeutic Management • Surgery to correct cardiac abnormalities, GI malformations and craniofacial deviations • Neck radiography before the child participates in any sports
  • 33. Nursing Management • Options for fluid and calorie intake – Breastfeeding may not be possible, immature sucking reflex – Special bottles and utensils • Routine – Changes causes frustration and decreased coping abilities • Encourage self-care • Advise X-rays before participating in sports
  • 35. Cold Stress • Infants lack shivering response • Norepinephrine (SNS) stimulates fat metabolism to produce internal heat  blood  surface tissues • Increased in metabolism  increased oxygen consumption • Norepinephrine  vasoconstriction  decrease oxygen decreased glucose metabolism • Results: Hypoxia, Metabolic acidosis, Hypoglycemia
  • 36. Three primary methods for maintaining a neutral thermal environment • Incubator • Radiant warming panel • Open bassinet with cotton blankets
  • 37. Temperature control • Warm items first • Plastic wrap • Careful drying • Kangaroo care
  • 38. Incubator Care • Double walled incubators –improve infants ability to maintain a desirable temp reduces energy expenditure r/t heat regulation • Pre-warm incubator first • Head covering when outside of the incubator
  • 39. Essential public strategy that enables the early detection and management of several congenital metabolic disorders, which if left untreated , may lead to mental retardation and even death For early detection and management of congenital metabolic disorders THE NEWBORN SCREENING PROGRAM
  • 40. Newborn Screening Program (NBS) • Mandated through RA 9288 (The Newborn Screening Act of 2004) • Done between 24-72 hours after birth
  • 41. Collection of NBS Samples • Through heel prick method: 4 drops of blood is drawn from heel puncture blotted onto a filter paper • Air dry 4-6 hours • Sent to laboratory within 24 hours • BEST - 48th to 72nd hours of life • ACCEPTABLE - anytime after 24 hours from birth until 2 weeks of age
  • 42. Sample collection done before the ideal time may result in: Falsely elevated thyroid stimulating hormone (TSH) = false (+) screen for CH Falsely elevated 17 hydroxyprogesterone (17-OH-P) = false (+) screeen for CH Falsely low galactose and phenylalalnine = false (-) screen for GAL and PKU
  • 43. Disorders tested for newborn screening • Congenital Hypothyroidism (CH) • Congenital Adrenal Hyperplasia (CAH) • Galactosemia (GAL) • Phenylketonuria (PKU) • Glucose-6-Phospate-Dehydrogenase Deficiency (G6PD)
  • 45. Congenital Hypothyroidism (CH) • aka Cretinism • Lack or absence of thyroid hormone
  • 46. (H-U-Mi-D) Hereditary conditions Underdevelopment of the fetal thyroid glands Maternal Intake of anti thyroid drugs during pregancy Deficiency, Maternal Iodine
  • 47. *Manifestations Poor suck and feeding Jaundice Hypotonia Cool pale dry skin Swelling around the eyes Large swollen tongue Large fontanels with late closure Poor weight gain and growth Hoare sounding cry Delayed milestone (sitting, crawling, walking and talking)
  • 48. *Treatment Lifetime oral doses of thyroid hormone. L- Thyroxine Nursing Considerations: Instruct parents to avoid Soy-based formulas and iron supplements. Avoid adjusting medications without MD’s order to prevent under medication or over medication.
  • 49. Excessive medication can cause : D-I-T-S Diarrhea Inability to sleep Tachycardia Shakiness in the child
  • 50. *Treatment Regular monitoring of the child’s weight, overall health and thyroid hormones level
  • 52. Congenital Adrenal Hyperplasia (CAH) • Excessive or deficient production of sex steroids • Severe salt loss, dehydration and abnormally high levels of male sex hormones in both boys and girls • If not detected and treated early, infants may die within 7-14 days
  • 53. Congenital Adrenal Hyperplasia (CAH) CAH is caused by a deficiency of adrenal gland hormones. 21 hydroxylase is missing or not working correctly.
  • 54. Congenital Adrenal Hyperplasia (CAH) 21-OH is responsible for the production of hormones : CORTISOL is involved in glucose metabolism and in normal inflammation and immune response. ALDOSTERONE is responsible for blood pressure and sodium retention.
  • 55. Congenital Adrenal Hyperplasia (CAH) *Manifestations • Poor feeding • Listlessness and drowsiness • Vomiting • Diarrhea • Weight loss • Hypotension • Hyponatremia • Metabolic acidosis
  • 56. Muscle growth at an early age Enlargement of penis during childhood
  • 57. Early deepening of the voice Early beard
  • 58. Pubic hair and underarm hair during childhood Severe acne
  • 59. M-E-E-E-P-S-S Muscle growth at an early age Enlargement of penis during childhood Early deepening of the voice Early beard Pubic hair and underarm hair during childhood Smaller than normal testicles
  • 61. Early puberty changes such as hair in airmpits and pubic area Lack of menstrual periods or scanty or irregular periods
  • 62. Excess hair on the face and body Deep, husky voice
  • 63. (S-M-E-L-E-D) Severe acne Male pattern baldness Early puberty changes such as hair in airmpits and pubic area Lack of menstrual periods or scanty or irregular periods Excess hair on the face and body Deep, husky voice
  • 64.
  • 65. *Treatment Lifetime administration of the deficient or missing hormones HYDROCORTISONES lessens the amount of androgens (prevents early puberty and allows for more typical growth and
  • 66. Over medication can results to Cushing’s syndrome (Stretch marks, rounded face, weight gain, hypertension and bone loss). Under medication can occur during periods of stress and illness when higher doses of the
  • 67. Corrective surgery for enlarged clitoris (can be done as early as one to three years of age. To separate labia and to
  • 69. Galactosemia (GAL) This hereditary disorder is characterized by the lack of the enzyme Galactose-1-Phosphate uridyl Transferase (GALT) that converts galactose to glucose, the form of sugar that can be used by body cells.
  • 70. Galactosemia (GAL) Initial symptoms also include: (F-L-I-P) Failure to gain weight Lethargy Irritability Poor feeding and poor suck
  • 71. Galactosemia (GAL) Treatment: Giving the child a special lactose free formula and exclusion of lactose and galactose foods such as milk (including breast milk) and other dairy products from the diet through out life.
  • 72. Galactosemia (GAL) Foods that should be avoided: Milk and all dairy products Processed and pre packaged foods Tomato sauces Certain medications Any foods or drugs which contain the ingredients Lactulose, Casein, Caseinate, Lactalbumin, Curds, Whey or Whey solids
  • 73. Galactosemia (GAL) Calcium and Vitamin D deficiency is likely to develop in a child on a lactose free. Therefor, the child is given supplements to prevent deficiencies
  • 75. Phenylketonuria (PKU) A metabolic disorder characterized by lack of enzyme Phenylalanine hydroxylase (PAH) needed to process the amino acid phenylalanine The resultant build up of the said protein in the body leads to mental retardation
  • 76. Phenylketonuria (PKU) • Excessive accumulation of phenylalanine = brain damage • Dx – Guthrie test • Mx - Low protein diet; breastmilk
  • 77. Glucose-6-Phospate-Dehydrogenase Deficiency (G6PD)
  • 78. G6PD is one of many enzymes that help the body process carbohydrates and turn them into energy.
  • 79. Glucose-6-Phospate-Dehydrogenase Deficiency (G6PD) • A condition where the body lacks the enzyme called G6PD a metabolic enzyme especially important in RBC metabolism • Hemolytic anemia resulting from exposure to certain drug, food and chemical
  • 81.
  • 82. STRESSORS AND THE CHILD’S REACTION Illness and Hospitalization:
  • 83. Children are particularly vulnerable to the crises of illness and hospitalization because: 1.Stress represents a change from the usual state of health and environmental routine 1.Children have limited number of coping mechanisms to resolve stressors
  • 84. SEPARATION ANXIETY • Also known as Anaclitic depression • Major stress especially for children ages 16 to 30 months • Three Phases: –Phase of Protest –Phase of Despair –Phase of Detachment
  • 85. SEPARATION ANXIETY Three Phases: Phase of Protest • React aggressively to separation from parent • Behavior is from a few hours to several days
  • 86. SEPARATION ANXIETY Three Phases: Phase of Despair •Child is less active •Withdraws from others
  • 87. SEPARATION ANXIETY Three Phases: Phase of Detachment • Also called denial • Appears detached and uninterested in parents’ visits • Appears to finally adjust to the surroundings
  • 88. Loss of Control INFANTS – Trust – Inconsistent care and deviations from daily routine • TODDLERS – Autonomy – Egocentric pleasures – Rely on the consistency and familiarity of daily rituals – Altered routine and rituals – Regression • PRESCHOOLERS – Egocentrism and magical thinking – Physical restriction, altered routines and enforced dependency
  • 89. Bodily Injury and Pain • INFANTS – Infants younger than 6 months • no obvious memory of previous pain – Facial expression of discomfort – React with physical resistance – Distraction and anticipatory preparation does little to lessen immediate reaction to pain • TODDLERS – Intrusive experience produce anxiety – React with intense emotional upset and physical resistance – Communicate about their pain
  • 90. Bodily Injury and Pain • PRESCHOOLERS – Cause of illness is seen as concrete action the child does or the child fails to do  self-blame – Contagion – proximity of two object or persons causes the illness – Injection - fear that the puncture will not close • SCHOOL-AGE CHILDREN – May be less concerned with pain than disability – Major concern is their fear of being told that something is wrong with them – Aware of the significance of different illnesses
  • 91. Bodily Injury and Pain • SCHOOL-AGE CHILDREN – Passive acceptance of pain – Nondirective request for support – When someone identifies unspoken messages and offers support, they readily accept it • ADOLESCENTS – The nature of bodily injury may be more important based on the adolescents’ perception rather than the actual degree of severity of the illness – Changes in body image is their concern – Privacy – Reluctance to disclose pain
  • 92. NURSING CARE OF THE CHILD WHO IS HOSPITALIZED
  • 93. Communication • Speak in quiet pleasant tones • Bend down • Do not use clichés. • Explain all procedures • Be honest • Be careful in making promises • Observe nonverbal communication for clues to level of understanding • Do not threaten • Allow child to show feelings • Provide time to talk
  • 94. Communication • Teach parents to anticipate next stage of development • If teaching is interrupted, start over from the beginning • Provide independence • Do not compare child’s progress to that of anyone else • Provide praise • Instead of asking what something is, ask child to give it a name or tell you about it • Allow choices where possible • Involve parents in child’s care
  • 95. Communication • Keep routines • If parents cannot stay with child, encourage them to bring in a favorite toy, pictures of family members or to make tape to played for the child
  • 96. Play
  • 97. • Toddler – Enjoys repetition – Solitary play – Parallel play • Preschooler – Role play, make believe, associative play • School-age – Group, organized activities – Group goals with interaction
  • 98. Play • Play is a very important part of development for your growing child. • Not only is play time entertaining for your child, but it also provides stimulation, increases skills and coordination, provides an outlet for your child's energy, and helps to encourage exploration by your child.
  • 99. Play is also important for the following reasons (Lippincott Williams & Wilkins, 2005) Play is an excellent stress reducer and tension reliever. It allows the child freedom of expression to act out his fears, concerns and anxieties
  • 100. Play is also important for the following reasons (Lippincott Williams & Wilkins, 2005) Play provides a source of diversional activity, alleviating separation anxiety
  • 101. Play is also important for the following reasons (Lippincott Williams & Wilkins, 2005) Play provides the child with a sense of safety and security because while he is engaging in play, he knows that no painful procedures will occur.
  • 102. Play is also important for the following reasons (Lippincott Williams & Wilkins, 2005) Developmentally appropriate play fosters the child’s normal growth and development, especially for children who are repeatedly hospitalized for chronic conditions
  • 103. Play is also important for the following reasons (Lippincott Williams & Wilkins, 2005) • Play puts the child in the driver’s seat, allowing him to make choices and giving him a sense of control
  • 104. Play – Way to solve problems – Express creativity – Decrease stress – Prepare for procedures – Enhance fine and motor skills • Make play appropriate for mental age and physical/disease state • Multisensory stimulation • Safe toys for mental age • Offer play specific to age group
  • 105. NURSING CARE OF THE CHILD IN PAIN
  • 106. Concept of Pain Preoperational Thought (2-7 yrs) Relates to pain primarily as physical concrete experience Magical disappearance of pain Pain as punishment Hold someone accountable for own pain Concrete Operational Thought (7-10 yrs) Relates to pain physically Perceive psychologic pain Fears bodily harm & annihilation Pain as punishment Formal Operational Thought (13 yrs and older) Give reason for pain Perceives several types of psychologic pain Fears losing control during painful experience
  • 107. Q-U-E-S-T (PAIN ASSESSMENT) QUESTION the child’s parents and child too, if he is old enough to respond USE appropriate pain assessment EVALUATE the child’s behaviour SECURE the parent’s active participation in treatment TAKE the cause of the pain into consideration
  • 108. ASSESSMENT • Wong-Baker FACES Pain Rating Scale
  • 109.
  • 110. ASSESSMENT • FLACC (Face, Legs, Activity, Cry and Consolability) – for infants and very young children • Behavior is observed to assess pain Measures each of the five identified categories on a 0 to 2 scale • The higher the total score, the more pain
  • 111.
  • 112. CRIES Neonatal Postoperative Pain Measurement Scale Crying Requires oxygen to maintain saturation about 95% Increased heart rate and blood pressure Expression Sleeplessness
  • 113. Neonatal Infant Pain Scale Facial Expression Crying Breathing patterns State of arousal Movement of arms and legs
  • 114. Premature Infant pain Profile Gestational age Heart rate Oxygen saturation Behavioral state Brow bulge Eye squeeze Nasolabial furrow
  • 115.
  • 116. INFANT Mouth stretched open Eyes tightly shut Facial expression Brows and forehead knitted Cheeks raised high enough
  • 117. Younger Children Narrowing of the eyes Grimace or fearful appearance Frequent and longer lasting bouts of crying with a tone that is higher and louder than normal Less receptiveness to comforting by parents or other caregivers Holding or protecting the painful areas
  • 118. P-A-I-N Management Pharmacologic interventions Anticipate and prevent or minimize pain related to hospitalization, procedure and treatment Identify and relieve existing pain Non pharmacologic interventions to reduce stress, increase comfort and enhance
  • 119. Pharmacologic Intervention – mainstay of pain management and it depends on the specific needs of the patient Opioid analgesics -Highly effective pain relievers and constitute the core of most pharmacologic interventions to manage acute pain in infants and children -Oral, sublingual, rectal, nasal, subcutaneous, transdermal, IV and intraspinal *Morphine (MS contin) *Fetanyl (Duragesic)
  • 120. Non Opioid Analgesics -are prescribed to manage mild to moderate pain. -infants and children metabolize non opioid analgesics in the same manner and at the same rate as adult.
  • 121. NSAIDS -relieve for mild to moderate pain and anti inflammatory effects -Ibuprofen (advil); Naproxen (Naprosyn); Tolmetin (Tolectin); Indomethacin (Indocin) & Ketorolac (Toradol) are approved for use in children -S.E: Inhibition of platelet aggregation and GI irritation
  • 122. Acetaminophen -Is the DOC for treating mild pain. Available in suppository, liquid and table form. -it has the added benefit of helping reduce fever and is very safe, even for neonates. -long term can cause risk of liver damage
  • 123. EMLA Cream (lidocaine 2.5% and prilocaine 2.5%), applied to intact skin under occlusive dressing, provides dermal analgesia by the release of lidocaine and prilocaine from the cream into the epidermal and dermal layers of the skin
  • 124. • Complementary and alternative medicine (CAM) – Complementary Pain Medicine • Music Therapy • Hypnosis • TENS (transcutaneous electric nerve stimulation) unit • Acupuncture – Non-Pharmacologic Care • Comfort, positioning and non-nutritive sucking • Distraction • Relaxation • Guided Imagery • Biofeedback • Behavioral Contracting
  • 126. Pediatric Surgery • Preoperative classes – Younger – simple and as close to the time of the procedure as possible • Allow to play with equipment • Teach and provide time to practice • Show pictures • Describe sensations • Detect misconceptions or fantasies • Parents can often be helpful in preparing
  • 127. PEDIATRIC SURGERY • Preoperative class • Listen to child for clarifying misunderstandings • Give simple information about the system that will be affected • Use of anatomically correct dolls • Preschool boys: allow to look at penis after surgery • Post surgery: helping child master a threatening situation and minimizing physical and psychological complications
  • 128. CHRONICALLY ILL PEDIATRIC CLIENTS: CONCEPTS OF DEATH DYING AND GRIEVING
  • 129. Concept of Death in Childhood (Lippincotts William and Wilkins, 2005) Infancy Concept of death – NONE Nursing considerations: Be aware that the older infant will experience separation anxiety Help the family cope with death so they can be available to the infant
  • 130. Concept of Death in Childhood (Lippincotts William and Wilkins, 2005) Early childhood Knows the words “DEAD” and “DEATH”. Reactions are influenced by the attitude of the parents. Nursing considerations: Help the family members including siblings cope with their feelings Allow the child to express his own feelings in an open and honest manner.
  • 131. Concept of Death in Childhood (Lippincotts William and Wilkins, 2005) Middle childhood. Understands universality and irreversibility of death. May have a fear of parents dying. Nursing considerations Use play to facilitate the child’s understanding of death Allow siblings to express their feelings.
  • 132. Concept of Death in Childhood (Lippincotts William and Wilkins, 2005) Late childhood Beings to incorporate family and cultural beliefs about death. Explores views of an afterlife and faces the reality of own mortality Nursing considerations Provide opportunities for the child to verbalize his fears Help the child discuss his concerns with the family
  • 133. Concept of Death in Childhood (Lippincotts William and Wilkins, 2005) Adolescence Adult perception of death, but still focused on the HERE and NOW Nursing considerations Use opportunities to open discussion about death Allow expression of feelings of guilt, confusion and anxiety Support and maintain self esteem
  • 134. Helping Families to Cope • Accept and support participants • Be available and express your availability • Encourage parents to assist in the care of their child • Encourage involvement of siblings • Religious associations as source of strength and support
  • 135. Helping parents to talk with their child about dying if he is ready to do so Encouraging all family members to express their feelings, even though they might be difficult to hear Allowing families to spend as much time as possible with the dying child Allowing and encouraging parents to continue to take an active role in their child’s care Reminding parents that they don’t always have to be strong and ask for help
  • 136. Thank you for Listening!

Editor's Notes

  1. NEC usually occurs within the first 2 weeks of life, usually after milk feeding has begun (at first, feedings are usually given through a tube that goes directly to the baby's stomach). About 10% of babies weighing less than 3 lbs.-5 oz. (1,500 grams) experience NEC. These premature infants have immature bowels, which are sensitive to changes in blood flow and prone to infection. They may have difficulty with blood and oxygen circulation and digestion, which increases their chances of developing NEC.
  2. The exact cause of NEC is unknown, but one theory is that the intestinal tissues of premature infants are weakened by too little oxygen or blood flow. So when feedings are started, the added stress of food moving through the intestine allows bacteria normally found in the intestine to invade and damage the wall of the intestinal tissues. The damage may affect only a short segment of the intestine or can progress quickly to involve a much larger portion. The infant is unable to continue feedings and starts to appear ill if bacteria continue to spread through the wall of the intestines and sometimes into the bloodstream. He or she may also develop imbalances in the minerals in the blood. In severe cases of NEC, a hole (perforation) may develop in the intestine, allowing bacteria to leak into the abdomen and cause life-threatening infection (peritonitis). Because the infant's body systems are immature, even with quick treatment for NEC there may be serious complications. Other factors seem to increase the risk of developing NEC. Some experts believe that the makeup of infant formula, the rate of delivery of the formula, or the immaturity of the mucous membranes in the intestines can cause NEC. (Babies who are fed breast milk can also develop NEC, but their risk is lower.)Another theory is that babies born through difficult deliveries with lowered oxygen levels can develop NEC. When there isn't enough oxygen, the body sends the available oxygen and blood to vital organs instead of the gastrointestinal tract, and NEC can result.Babies with an increased number of red blood cells (polycythemia) in circulation also seem to be at higher risk for NEC. Too many red blood cells thicken the blood and hinder the transport of oxygen to the intestines.NEC sometimes seems to occur in "epidemics," affecting several infants in the same nursery. Although this may be due to coincidence, it suggests the possibility that it could in some cases be spread from one baby to another, despite the fact that all nurseries have very strict precautions to prevent the spread of infection.Theories to Support that Explains NECLittle supply of oxygenation -> plus feeding -> stress to the intestinal wall -> allowing bacteria to invade intestinal wall and bloodstream -> necrosis/perforation of the intestinal wall -> decrease absorption of the vitamins and minerals and Leak of bacteria into abdomen causing peritonitis.Difficult deliveries -> deprived oxygenation -> vital organs receives more oxygenIncreased RBC counts – thickens the blood and impaired circulation -> hinder the transport of oxgenation
  3. The exact cause of NEC is unknown, but one theory is that the intestinal tissues of premature infants are weakened by too little oxygen or blood flow. So when feedings are started, the added stress of food moving through the intestine allows bacteria normally found in the intestine to invade and damage the wall of the intestinal tissues. The damage may affect only a short segment of the intestine or can progress quickly to involve a much larger portion.The infant is unable to continue feedings and starts to appear ill if bacteria continue to spread through the wall of the intestines and sometimes into the bloodstream. He or she may also develop imbalances in the minerals in the blood.In severe cases of NEC, a hole (perforation) may develop in the intestine, allowing bacteria to leak into the abdomen and cause life-threatening infection (peritonitis). Because the infant's body systems are immature, even with quick treatment for NEC there may be serious complications.Other factors seem to increase the risk of developing NEC. Some experts believe that the makeup of infant formula, the rate of delivery of the formula, or the immaturity of the mucous membranes in the intestines can cause NEC. (Babies who are fed breast milk can also develop NEC, but their risk is lower.)Another theory is that babies born through difficult deliveries with lowered oxygen levels can develop NEC. When there isn't enough oxygen, the body sends the available oxygen and blood to vital organs instead of the gastrointestinal tract, and NEC can result.Babies with an increased number of red blood cells (polycythemia) in circulation also seem to be at higher risk for NEC. Too many red blood cells thicken the blood and hinder the transport of oxygen to the intestines.NEC sometimes seems to occur in "epidemics," affecting several infants in the same nursery. Although this may be due to coincidence, it suggests the possibility that it could in some cases be spread from one baby to another, despite the fact that all nurseries have very strict precautions to prevent the spread of infection.
  4. Signs and SymptomsThe symptoms of NEC can resemble those of other digestive conditions, and may vary from infant to infant. Common symptoms include:poor tolerance to feedingsfeedings stay in stomach longer than expecteddecreased bowel soundsabdominal distension (bloating) and tendernessgreenish (bile-colored) vomitredness of the abdomenincrease in stools, or lack of stoolsbloody stoolsMore subtle signs of NEC might include apnea (periodic stoppage of breathing), bradycardia (slowed heart rate), diarrhea, lethargy, and fluctuating body temperature. Advanced cases may show fluid in the peritoneal (abdominal) cavity, peritonitis (infection of the membrane lining the abdomen), or shock.Diagnosis and TreatmentThe diagnosis of NEC is usually confirmed by the presence of an abnormal gas pattern as seen on an X-ray. This is indicated by a "bubbly" appearance of gas in the walls of the intestine, large veins of the liver, or the presence of air outside of the intestines in the abdominal cavity. A surgeon may insert a needle into the abdominal cavity to withdraw fluid to determine whether there is a hole in the intestines.
  5. NPO – confirmed NECAdministered thru enteral feedings – decrease incidence of NECMost infants with NEC are treated medically, and symptoms end without the need for surgery. Treatment includes:stopping feedingsnasogastric drainage (inserting a tube through the nasal passages down to the stomach to remove air and fluid from the stomach and intestine)intravenous (IV) fluids for fluid replacement and nutritionantibiotics for infectionfrequent examinations and X-rays of the abdomenThe baby's belly size is measured and watched carefully, and periodic blood samples are taken to look for bacteria. Stools are also checked for blood. If the abdomen is so swollen that it interferes with breathing, extra oxygen or mechanically assisted breathing (a ventilator) is used to help the baby breathe.A baby who responds favorably may be back on regular feedings within 72 hours, although in most cases feedings are withheld and antibiotics are continued for 7 to 10 days. If the bowel perforates (tears) or the condition worsens, surgery may be indicated. Severe cases of NEC may require removal of a segment of intestine. Sometimes after removal of diseased bowel, the healthy areas can be sewn back together. Other times, especially if the baby is very ill or there is spillage of stool in the abdomen, the surgeon will bring an area of the intestine or bowel to an opening on the abdomen (called an ostomy). Most infants who develop NEC recover fully and do not have further feeding problems. In some cases, scarring and narrowing of the bowel may occur and can cause future intestinal obstruction or blockage. Another residual problem may be malabsorption (the inability of the bowel to absorb nutrients normally). This is more common in children who required surgery for NEC and had part of their intestine removed.
  6. per rectum – increase danger of perforationPosition – avoid pressure on distended abdomenFacilitate observation
  7. Some newborns' breathing during the first hours of life is more rapid and labored than normal because of a lung condition called transient tachypnea of the newborn (TTN).About 1% of all newborns develop TTN, which usually eases after a few days with treatment. Babies born with TTN need special monitoring and treatment while in the hospital, but afterwards most make a full recovery, with no lasting effect on growth and development.About TTNBefore birth, a fetus' lungs are filled with fluid. While inside the mother, a fetus does not use the lungs to breathe — all oxygen comes from the blood vessels of the placenta.As the due date nears, the baby's lungs begin to clear the fluid in response to hormonal changes. Some fluid may also be squeezed out during the birth, as a baby passes through the birth canal. After the birth, as a newborn takes those first breaths, the lungs fill with air and more fluid is pushed out of the lungs. Any remaining fluid is then coughed out or gradually absorbed into the body through the bloodstream and lymphatic system.In infants with TTN, however, extra fluid in the lungs remains or the fluid is cleared too slowly. So it is more difficult for the baby to inhale oxygen properly, and the baby breathes faster and harder to get enough oxygen into the lungs.Causes of TTNTTN, also called "wet lungs" or type II respiratory distress syndrome, usually can be diagnosed in the hours after birth. It's not possible to detect before the birth whether a child will have it.TTN can occur in both preemies (because their lungs are not yet fully developed) and full-term babies.Newborns at higher risk for TTN include those who are:delivered by cesarean section (C-section)born to mothers with diabetesborn to mothers with asthmasmall for gestational age (small at birth)During vaginal births, especially with full-term babies, the pressure of passing through the birth canal squeezes some of the fluid out of the lungs. Hormonal changes during labor may also lead to absorption of some of the fluid.Babies who are small or premature or who are delivered via rapid vaginal deliveries or C-section don't undergo the usual squeezing and hormone changes of a vaginal birth. So they tend to have more fluid than normal in their lungs when they take their first breaths.
  8. A respiratory problem seen in the newborn shortly after deliveryIt is likely due to retained lung fluid, and common in 35+ week gestation babies who are delivered by caesarian section without laborUsually, this condition resolves over 24-48 hours.Pulmonary immaturity has also been proposed as a causative factor.Mild surfactant deficiency has also been suggested as a causative factor.
  9. (higher than the normal range of 40-60 times per minute)
  10. Antigens –foreign body capable of producing immune response if recognized by the body as foreignIn Rh system, the person must be exposed to the Rh antigen before significant antibody formation takes place and causes sensitivity response called isoimmunizationHydropsand hemolysis causes hypoxia, cardiac failure (fetus) generalized edema (anasarca) and pleural effusionMay be delivered still born or in severe respiratory distressRh positive – present Rh factorPh negative - absence
  11. Jaundice –first 24 hours increase bili liver’s inability to conjugate excess biliAnemia – hemolysisHypogly – pancreatic hyperplasia
  12. RhIg (RhoGAM) – must be administered to unsensitized mothers within 72 hours after the first deliveryAdmin of RhIg at 26 to 28 weeks of gestation further reduces risk of isoimmunization
  13. RhIg (RhoGAM) – must be administered to unsensitized mothers within 72 hours after the first deliveryAdmin of RhIg at 26 to 28 weeks of gestation further reduces risk of isoimmunization
  14. Amount exchanged and infused
  15. 3 representatives of chromosome 21 are present instead of the usual 2
  16. Extra chromosome 21  trisomy 21-greater risk for older women - > 35 years of agePaternal age factor, 55 years of age or older
  17. Epicanthal – extra fold at the inner canthusIris may have white specks(bradycephaly) Head size is usually smaller that 10th – 20th percentileRag-doll appearance – poor muscle toneSimian line – a single horinzontal palm crease rather than the usual crease
  18. PN testing – amniocentesis chorionic villus sampling
  19. Lack shivering response  produces heat through increased metabolic process 
  20. Warm items first – reduce heat loss
  21. Head covering to prevent heat loss
  22. Essential public strategy that enables the early detection and management of several congenital metabolic disorders, which if left untreated , may lead to mental retardation and even deathFor early detection and management of congenital metabolic disorders
  23. A simple procedure to find out if the infant has medical condition that can result to mental retardation or even death if not treated.Air dry in 4-6 hoursSent to the lab within 24 hours
  24. Samples taken less than 24 hours from birth require repeat screening at 2 weeks of ageSample collection done before the ideal time may result in:Falsely elevated thyroid stimulating hormone (TSH) = false (+) screen for CHFalsely elevated 17 hydroxyprogesterone (17-OH-P) = false (+) screeen for CHFalsely low galactose and phenylalalnine = false (-) screen for GAL and PKU
  25. Congenital Hypothyroidism*this is a congenital metabolic disorder characterized by insufficient thyroid hormones that result in retarded growth and brain development.*this disorder can be used by congenital absence of underdevelopment of the fetal thyroid glands, hereditary conditions, maternal iodine deficiency and maternal intake of anti thyroid drugs during pregancy (H-U-Mi-D)*NB with this d/o do not exhibit symptoms because of the presence of maternal thyroid hormones in their body. After 2 to 3 weeks, MTH are depleted and the infant must rely on its own TG to produce the hormones.
  26. Thyroid hormone - which is essential to growth of the brain and the bodyNeonates who are born without the ability to synthesize adequate amounts of thyroid hormoneDelayed development of the nervous system
  27. Congenital Hypothyroidism*this is a congenital metabolic disorder characterized by insufficient thyroid hormones that result in retarded growth and brain development.*this disorder can be used by congenital absence of underdevelopment of the fetal thyroid glands, hereditary conditions, maternal iodine deficiency and maternal intake of anti thyroid drugs during pregancy (H-U-Mi-D)*NB with this d/o do not exhibit symptoms because of the presence of maternal thyroid hormones in their body. After 2 to 3 weeks, MTH are depleted and the infant must rely on its own TG to produce the hormones.
  28. Congenital Hypothyroidism*this is a congenital metabolic disorder characterized by insufficient thyroid hormones that result in retarded growth and brain development.*this disorder can be used by congenital absence of underdevelopment of the fetal thyroid glands, hereditary conditions, maternal iodine deficiency and maternal intake of anti thyroid drugs during pregancy (H-U-Mi-D)*NB with this d/o do not exhibit symptoms because of the presence of maternal thyroid hormones in their body. After 2 to 3 weeks, MTH are depleted and the infant must rely on its own TG to produce the hormones.*ManifestationsPoor suck and feedingJaundiceHypotoniaCool pale dry skinSwelling around the eyesLarge swollen tongueLarge fontanels with late closurePoor weight gain and growthHoare sounding cryDelayed milestone (sitting, crawling, walking and talking)*TreatmentLifetime oral doses of thyroid hormone. L-Thyroxine, to promote normal development and mixed with food or formula. Instruct parents to avoid Soy-based formulas and iron supplements. Avoid adjusting medications without MD’s order to prevent under medication or over medication. Excessive medication can cause D-I-T-S Diarrhea, Inability to sleep, Tachycardia, Shakiness in the child
  29. Congenital Hypothyroidism*this is a congenital metabolic disorder characterized by insufficient thyroid hormones that result in retarded growth and brain development.*this disorder can be used by congenital absence of underdevelopment of the fetal thyroid glands, hereditary conditions, maternal iodine deficiency and maternal intake of anti thyroid drugs during pregancy (H-U-Mi-D)*NB with this d/o do not exhibit symptoms because of the presence of maternal thyroid hormones in their body. After 2 to 3 weeks, MTH are depleted and the infant must rely on its own TG to produce the hormones.*ManifestationsPoor suck and feedingJaundiceHypotoniaCool pale dry skinSwelling around the eyesLarge swollen tongueLarge fontanels with late closurePoor weight gain and growthHoare sounding cryDelayed milestone (sitting, crawling, walking and talking)*TreatmentLifetime oral doses of thyroid hormone. L-Thyroxine, to promote normal development and mixed with food or formula. Instruct parents to avoid Soy-based formulas and iron supplements. Avoid adjusting medications without MD’s order to prevent under medication or over medication. Excessive medication can cause D-I-T-S Diarrhea, Inability to sleep, Tachycardia, Shakiness in the child
  30. Congenital Hypothyroidism*this is a congenital metabolic disorder characterized by insufficient thyroid hormones that result in retarded growth and brain development.*this disorder can be used by congenital absence of underdevelopment of the fetal thyroid glands, hereditary conditions, maternal iodine deficiency and maternal intake of anti thyroid drugs during pregancy (H-U-Mi-D)*NB with this d/o do not exhibit symptoms because of the presence of maternal thyroid hormones in their body. After 2 to 3 weeks, MTH are depleted and the infant must rely on its own TG to produce the hormones.*ManifestationsPoor suck and feedingJaundiceHypotoniaCool pale dry skinSwelling around the eyesLarge swollen tongueLarge fontanels with late closurePoor weight gain and growthHoare sounding cryDelayed milestone (sitting, crawling, walking and talking)*TreatmentLifetime oral doses of thyroid hormone. L-Thyroxine, to promote normal development and mixed with food or formula. Instruct parents to avoid Soy-based formulas and iron supplements. Avoid adjusting medications without MD’s order to prevent under medication or over medication. Excessive medication can cause D-I-T-S Diarrhea, Inability to sleep, Tachycardia, Shakiness in the child
  31. Congenital Hypothyroidism*this is a congenital metabolic disorder characterized by insufficient thyroid hormones that result in retarded growth and brain development.*this disorder can be used by congenital absence of underdevelopment of the fetal thyroid glands, hereditary conditions, maternal iodine deficiency and maternal intake of anti thyroid drugs during pregancy (H-U-Mi-D)*NB with this d/o do not exhibit symptoms because of the presence of maternal thyroid hormones in their body. After 2 to 3 weeks, MTH are depleted and the infant must rely on its own TG to produce the hormones.*ManifestationsPoor suck and feedingJaundiceHypotoniaCool pale dry skinSwelling around the eyesLarge swollen tongueLarge fontanels with late closurePoor weight gain and growthHoare sounding cryDelayed milestone (sitting, crawling, walking and talking)*TreatmentLifetime oral doses of thyroid hormone. L-Thyroxine, to promote normal development and mixed with food or formula. Instruct parents to avoid Soy-based formulas and iron supplements. Avoid adjusting medications without MD’s order to prevent under medication or over medication. Excessive medication can cause D-I-T-S Diarrhea, Inability to sleep, Tachycardia, Shakiness in the childRegular monitoring of the child’s weight, overall health and thyroid hormones level
  32. CAH is caused by a deficiency of adrenal gland hormones. This disorder develops when a particular enzyme called 21 hydroxylase is missing or not working correctly.21-OH is responsible for the production of hormones in cortisol and aldosterone in the adrenal glands. CORTISOL is involved in glucose metabolism and in normal inflammation and immune response. ALDOSTERONE is responsible for blood pressure and sodium retention. Excessive androgens, since it is produced by the adrenal glands.*ManifestationsPoor feedingListlessness and drowsinessVomitingDiarrheaWeight lossHypotensionHyponatremiaMetabolic acidosisUntreated boys may have some of the following traits: M-E-E-E-P-S-SMuscle growth at an early ageEnlargement of penis during childhoodEarly deepening of the voiceEarly beardPubic hair and underarm hair during childhoodSmaller than normal testiclesSevere acneUntreated girls may develop male like traits and behaviors, called VIRILIZATION. (S-M-E-L-E-D)Severe acneMale pattern baldnessEarly puberty changes such as hair in airmpits and pubic areaLack of menstrual periods or scanty or irregular periodsExcess hair on the face and bodyDeep, husky voice
  33. CAH is caused by a deficiency of adrenal gland hormones. This disorder develops when a particular enzyme called 21 hydroxylase is missing or not working correctly.21-OH is responsible for the production of hormones in cortisol and aldosterone in the adrenal glands. CORTISOL is involved in glucose metabolism and in normal inflammation and immune response. ALDOSTERONE is responsible for blood pressure and sodium retention. Excessive androgens, since it is produced by the adrenal glands.*ManifestationsPoor feedingListlessness and drowsinessVomitingDiarrheaWeight lossHypotensionHyponatremiaMetabolic acidosisUntreated boys may have some of the following traits: M-E-E-E-P-S-SMuscle growth at an early ageEnlargement of penis during childhoodEarly deepening of the voiceEarly beardPubic hair and underarm hair during childhoodSmaller than normal testiclesSevere acneUntreated girls may develop male like traits and behaviors, called VIRILIZATION. (S-M-E-L-E-D)Severe acneMale pattern baldnessEarly puberty changes such as hair in airmpits and pubic areaLack of menstrual periods or scanty or irregular periodsExcess hair on the face and bodyDeep, husky voice
  34. CAH is caused by a deficiency of adrenal gland hormones. This disorder develops when a particular enzyme called 21 hydroxylase is missing or not working correctly.21-OH is responsible for the production of hormones in cortisol and aldosterone in the adrenal glands. CORTISOL is involved in glucose metabolism and in normal inflammation and immune response. ALDOSTERONE is responsible for blood pressure and sodium retention. Excessive androgens, since it is produced by the adrenal glands.*ManifestationsPoor feedingListlessness and drowsinessVomitingDiarrheaWeight lossHypotensionHyponatremiaMetabolic acidosisUntreated boys may have some of the following traits: M-E-E-E-P-S-SMuscle growth at an early ageEnlargement of penis during childhoodEarly deepening of the voiceEarly beardPubic hair and underarm hair during childhoodSmaller than normal testiclesSevere acneUntreated girls may develop male like traits and behaviors, called VIRILIZATION. (S-M-E-L-E-D)Severe acneMale pattern baldnessEarly puberty changes such as hair in airmpits and pubic areaLack of menstrual periods or scanty or irregular periodsExcess hair on the face and bodyDeep, husky voice*TreatmentLifetime administration of the deficient or missing hormones HYDROCORTISONES lessens the amount of androgens (prevents early puberty and allows for more typical growth and development) *Monitor child’s growth, BP and hormone levels throughout childhood to prevent under or over medication. Over medication can results to Cushing’s syndrome (Stretch marks, rounded face, weight gain, hypertension and bone loss). Under medication can occur during periods of stress and illness when higher doses of the drug are required by the bodyCorrective surgery for enlarged clitoris (can be done as early as one to three years of age. To separate labia and to create a normal vagina
  35. CAH is caused by a deficiency of adrenal gland hormones. This disorder develops when a particular enzyme called 21 hydroxylase is missing or not working correctly.21-OH is responsible for the production of hormones in cortisol and aldosterone in the adrenal glands. CORTISOL is involved in glucose metabolism and in normal inflammation and immune response. ALDOSTERONE is responsible for blood pressure and sodium retention. Excessive androgens, since it is produced by the adrenal glands.*ManifestationsPoor feedingListlessness and drowsinessVomitingDiarrheaWeight lossHypotensionHyponatremiaMetabolic acidosisUntreated boys may have some of the following traits: M-E-E-E-P-S-SMuscle growth at an early ageEnlargement of penis during childhoodEarly deepening of the voiceEarly beardPubic hair and underarm hair during childhoodSmaller than normal testiclesSevere acneUntreated girls may develop male like traits and behaviors, called VIRILIZATION. (S-M-E-L-E-D)Severe acneMale pattern baldnessEarly puberty changes such as hair in airmpits and pubic areaLack of menstrual periods or scanty or irregular periodsExcess hair on the face and bodyDeep, husky voice
  36. Muscle growth at an early ageEnlargement of penis during childhoodEarly deepening of the voiceEarly beardPubic hair and underarm hair during childhoodSmaller than normal testiclesSevere acne
  37. Muscle growth at an early ageEnlargement of penis during childhoodEarly deepening of the voiceEarly beardPubic hair and underarm hair during childhoodSmaller than normal testiclesSevere acne
  38. Muscle growth at an early ageEnlargement of penis during childhoodEarly deepening of the voiceEarly beardPubic hair and underarm hair during childhoodSmaller than normal testiclesSevere acne
  39. Untreated boys may have some of the following traits: M-E-E-E-P-S-SMuscle growth at an early ageEnlargement of penis during childhoodEarly deepening of the voiceEarly beardPubic hair and underarm hair during childhoodSmaller than normal testiclesSevere acneUntreated girls may develop male like traits and behaviors, called VIRILIZATION. (S-M-E-L-E-D)Severe acneMale pattern baldnessEarly puberty changes such as hair in airmpits and pubic areaLack of menstrual periods or scanty or irregular periodsExcess hair on the face and bodyDeep, husky voice
  40. Untreated boys may have some of the following traits: M-E-E-E-P-S-SMuscle growth at an early ageEnlargement of penis during childhoodEarly deepening of the voiceEarly beardPubic hair and underarm hair during childhoodSmaller than normal testiclesSevere acneUntreated girls may develop male like traits and behaviors, called VIRILIZATION. (S-M-E-L-E-D)Severe acneMale pattern baldnessEarly puberty changes such as hair in airmpits and pubic areaLack of menstrual periods or scanty or irregular periodsExcess hair on the face and bodyDeep, husky voice
  41. Untreated boys may have some of the following traits: M-E-E-E-P-S-SMuscle growth at an early ageEnlargement of penis during childhoodEarly deepening of the voiceEarly beardPubic hair and underarm hair during childhoodSmaller than normal testiclesSevere acneUntreated girls may develop male like traits and behaviors, called VIRILIZATION. (S-M-E-L-E-D)Severe acneMale pattern baldnessEarly puberty changes such as hair in airmpits and pubic areaLack of menstrual periods or scanty or irregular periodsExcess hair on the face and bodyDeep, husky voice
  42. CAH is caused by a deficiency of adrenal gland hormones. This disorder develops when a particular enzyme called 21 hydroxylase is missing or not working correctly.21-OH is responsible for the production of hormones in cortisol and aldosterone in the adrenal glands. CORTISOL is involved in glucose metabolism and in normal inflammation and immune response. ALDOSTERONE is responsible for blood pressure and sodium retention. Excessive androgens, since it is produced by the adrenal glands.*ManifestationsPoor feedingListlessness and drowsinessVomitingDiarrheaWeight lossHypotensionHyponatremiaMetabolic acidosisUntreated boys may have some of the following traits: M-E-E-E-P-S-SMuscle growth at an early ageEnlargement of penis during childhoodEarly deepening of the voiceEarly beardPubic hair and underarm hair during childhoodSmaller than normal testiclesSevere acneUntreated girls may develop male like traits and behaviors, called VIRILIZATION. (S-M-E-L-E-D)Severe acneMale pattern baldnessEarly puberty changes such as hair in airmpits and pubic areaLack of menstrual periods or scanty or irregular periodsExcess hair on the face and bodyDeep, husky voice*TreatmentLifetime administration of the deficient or missing hormones HYDROCORTISONES lessens the amount of androgens (prevents early puberty and allows for more typical growth and development) *Monitor child’s growth, BP and hormone levels throughout childhood to prevent under or over medication. Over medication can results to Cushing’s syndrome (Stretch marks, rounded face, weight gain, hypertension and bone loss). Under medication can occur during periods of stress and illness when higher doses of the drug are required by the bodyCorrective surgery for enlarged clitoris (can be done as early as one to three years of age. To separate labia and to create a normal vagina
  43. CAH is caused by a deficiency of adrenal gland hormones. This disorder develops when a particular enzyme called 21 hydroxylase is missing or not working correctly.21-OH is responsible for the production of hormones in cortisol and aldosterone in the adrenal glands. CORTISOL is involved in glucose metabolism and in normal inflammation and immune response. ALDOSTERONE is responsible for blood pressure and sodium retention. Excessive androgens, since it is produced by the adrenal glands.*ManifestationsPoor feedingListlessness and drowsinessVomitingDiarrheaWeight lossHypotensionHyponatremiaMetabolic acidosisUntreated boys may have some of the following traits: M-E-E-E-P-S-SMuscle growth at an early ageEnlargement of penis during childhoodEarly deepening of the voiceEarly beardPubic hair and underarm hair during childhoodSmaller than normal testiclesSevere acneUntreated girls may develop male like traits and behaviors, called VIRILIZATION. (S-M-E-L-E-D)Severe acneMale pattern baldnessEarly puberty changes such as hair in airmpits and pubic areaLack of menstrual periods or scanty or irregular periodsExcess hair on the face and bodyDeep, husky voice*TreatmentLifetime administration of the deficient or missing hormones HYDROCORTISONES lessens the amount of androgens (prevents early puberty and allows for more typical growth and development) *Monitor child’s growth, BP and hormone levels throughout childhood to prevent under or over medication. Over medication can results to Cushing’s syndrome (Stretch marks, rounded face, weight gain, hypertension and bone loss). Under medication can occur during periods of stress and illness when higher doses of the drug are required by the bodyCorrective surgery for enlarged clitoris (can be done as early as one to three years of age. To separate labia and to create a normal vagina
  44. This hereditary disorder is characterized by the lack of the enzyme Galactose-1-Phosphate uridylTransferase (GALT) that converts galactose to glucose, the form of sugar that can be used by body cells.Build up of galatactose in the body resutls in blindness, severe mental retardation, growth deficiency and deathInfants with galactosemia usually have diarrhea and vomiting within a few days of drinking ilk or formula containing lactose, initial symptoms also include (F-L-I-P)Failure to gain weightLethargyIrritabilityPoor feeding and poor suckWithout treatment, the infant may exhibit hypoglycemia, seizures, hepatomegaly, jaundice, bleeding, serious infections and cataractsTreatment: Giving the child a special lactose free formula and exclusion of lactose and galactose foods such as milk (including breast milk) and other dairy products from the diet through out life.Foods that should be avoided:Milk and all dairy productsProcessed and pre packaged foodsTomato saucesCertain medications
  45. This hereditary disorder is characterized by the lack of the enzyme Galactose-1-Phosphate uridylTransferase (GALT) that converts galactose to glucose, the form of sugar that can be used by body cells.Build up of galatactose in the body resutls in blindness, severe mental retardation, growth deficiency and deathInfants with galactosemia usually have diarrhea and vomiting within a few days of drinking ilk or formula containing lactose, initial symptoms also include (F-L-I-P)Failure to gain weightLethargyIrritabilityPoor feeding and poor suckWithout treatment, the infant may exhibit hypoglycemia, seizures, hepatomegaly, jaundice, bleeding, serious infections and cataractsTreatment: Giving the child a special lactose free formula and exclusion of lactose and galactose foods such as milk (including breast milk) and other dairy products from the diet through out life.Foods that should be avoided:Milk and all dairy productsProcessed and pre packaged foodsTomato saucesCertain medications
  46. This hereditary disorder is characterized by the lack of the enzyme Galactose-1-Phosphate uridylTransferase (GALT) that converts galactose to glucose, the form of sugar that can be used by body cells.Build up of galatactose in the body resutls in blindness, severe mental retardation, growth deficiency and deathInfants with galactosemia usually have diarrhea and vomiting within a few days of drinking ilk or formula containing lactose, initial symptoms also include (F-L-I-P)Failure to gain weightLethargyIrritabilityPoor feeding and poor suckWithout treatment, the infant may exhibit hypoglycemia, seizures, hepatomegaly, jaundice, bleeding, serious infections and cataractsTreatment: Giving the child a special lactose free formula and exclusion of lactose and galactose foods such as milk (including breast milk) and other dairy products from the diet through out life.Foods that should be avoided:Milk and all dairy productsProcessed and pre packaged foodsTomato saucesCertain medications
  47. This hereditary disorder is characterized by the lack of the enzyme Galactose-1-Phosphate uridylTransferase (GALT) that converts galactose to glucose, the form of sugar that can be used by body cells.Build up of galatactose in the body resutls in blindness, severe mental retardation, growth deficiency and deathInfants with galactosemia usually have diarrhea and vomiting within a few days of drinking ilk or formula containing lactose, initial symptoms also include (F-L-I-P)Failure to gain weightLethargyIrritabilityPoor feeding and poor suckWithout treatment, the infant may exhibit hypoglycemia, seizures, hepatomegaly, jaundice, bleeding, serious infections and cataractsTreatment: Giving the child a special lactose free formula and exclusion of lactose and galactose foods such as milk (including breast milk) and other dairy products from the diet through out life.Foods that should be avoided:Milk and all dairy productsProcessed and pre packaged foodsTomato saucesCertain medicationsAny foods or drugs which contain the ingredients Lactulose, Casein, Caseinate, Lactalbumin, Curds, Whey or Whey solidsCalcium and Vitamin D deficiency is likely to develop in a child on a lactose free. Therefor, the child is given supplements to prevent deficiences
  48. This hereditary disorder is characterized by the lack of the enzyme Galactose-1-Phosphate uridylTransferase (GALT) that converts galactose to glucose, the form of sugar that can be used by body cells.Build up of galatactose in the body resutls in blindness, severe mental retardation, growth deficiency and deathInfants with galactosemia usually have diarrhea and vomiting within a few days of drinking ilk or formula containing lactose, initial symptoms also include (F-L-I-P)Failure to gain weightLethargyIrritabilityPoor feeding and poor suckWithout treatment, the infant may exhibit hypoglycemia, seizures, hepatomegaly, jaundice, bleeding, serious infections and cataractsTreatment: Giving the child a special lactose free formula and exclusion of lactose and galactose foods such as milk (including breast milk) and other dairy products from the diet through out life.Foods that should be avoided:Milk and all dairy productsProcessed and pre packaged foodsTomato saucesCertain medicationsAny foods or drugs which contain the ingredients Lactulose, Casein, Caseinate, Lactalbumin, Curds, Whey or Whey solidsCalcium and Vitamin D deficiency is likely to develop in a child on a lactose free. Therefor, the child is given supplements to prevent deficiencies
  49. A metabolic disorder in which the body cannot properly use one of the building blocks of protein called phenylalanineGuthrie testLow protein dietBreastmilk – low in phenylalanineA metabolic disorder characterized by lack of enzyme Phenylalanine hydroxylase (PAH) needed to process the amino acid phenylalanine, a proteiin that is found in almost every food, except pure fat and sugar. The resultant build up of the said protein in the body leads to mental retardation
  50. It is a metabolic enzyme involved in the pentose phosphate pathway, especially important in red blood cell metabolism.G6PD deficiency is an inherited condition in which the body doesn't have enough of the enzyme glucose-6-phosphate dehydrogenase, or G6PD, which helps red blood cells (RBCs) function normally. This deficiency can cause hemolyticanemia, usually after exposure to certain medications, foods, or even infections. Most people with G6PD deficiency don't have any symptoms, while others develop symptoms of anemia only after RBCs have been destroyed, a condition called hemolysis. In these cases, the symptoms disappear once the cause, or trigger, is removed. In rare cases, G6PD deficiency leads to chronic anemia. With the right precautions, a child with G6PD deficiency can lead a healthy and active life.About G6PD DeficiencyG6PD is one of many enzymes that help the body process carbohydrates and turn them into energy. G6PD also protects red blood cells from potentially harmful by products that can accumulate when a person takes certain medications or when the body is fighting an infection.In people with G6PD deficiency, either the RBCs do not make enough G6PD or what is produced cannot properly function. Without enough G6PD to protect them, RBCs can be damaged or destroyed. Hemolyticanemia occurs when the bone marrow (the soft, spongy part of the bone that produces new blood cells) cannot compensate for this destruction by increasing its production of RBCs.
  51. Children are particularly vulnerable to the crises of illness and hospitalization because:Stress represents a change from the usual state of health and environmental routineChildren have limited number of coping mechanisms to resolve stressorsReactions depend on their developmental age
  52. Children are particularly vulnerable to the crises of illness and hospitalization because:Stress represents a change from the usual state of health and environmental routineChildren have limited number of coping mechanisms to resolve stressorsReactions depend on their developmental age
  53. Detachment occurs usually after prolonged separation from parentsPhase of ProtestReact aggressively to separation from parentBehavior is from a few hours to several daysPhase of DespairChild is less activeUninterested in play or foodWithdraws from othersSad, lonely, apatheticStops cryingDepression is evidentPhase of DetachmentAlso called denialAppears to finally adjust to the surroundingsCopes by forming superficial relationships with othersNot a sign of contentment
  54. Detachment occurs usually after prolonged separation from parentsPhase of ProtestReact aggressively to separation from parentBehavior is from a few hours to several daysPhase of DespairChild is less activeUninterested in play or foodWithdraws from othersSad, lonely, apatheticStops cryingDepression is evidentPhase of DetachmentAlso called denialAppears to finally adjust to the surroundingsCopes by forming superficial relationships with othersNot a sign of contentment
  55. Detachment occurs usually after prolonged separation from parentsPhase of ProtestReact aggressively to separation from parentBehavior is from a few hours to several daysPhase of DespairChild is less activeUninterested in play or foodWithdraws from othersSad, lonely, apatheticStops cryingDepression is evidentPhase of DetachmentAlso called denialAppears to finally adjust to the surroundingsCopes by forming superficial relationships with othersNot a sign of contentment
  56. Increases the perception of threatCan affect child's coping skillsGreatly depend on their age:
  57. Fear of bodily Injury and Pain-pain in childhood brings trauma during adulthood and tend to avoid medical careNurses must appreciate their concerns about bodily harm and reactions to painToddler – definition of body boundaries is poorly developed
  58. Speak in quiet pleasant tonesBend down to meet child on own levelUse words appropriate to age/communication ability; do not use clichés.Do not explain more than necessaryExplain all procedures and the reason for itBe honestDo not make a promise that you cannot keepObserve nonverbal communication for clues to level of understandingDo not threaten; and when necessary, punish the act not the child (I like you but not what you did)Allow child to show feelings, provide therapeutic play, pounding or throwing toys, allow child to cry, encourage drawing and creative drawing
  59. Teach parents to anticipate next stage of developmentIf teaching is interrupted, start over from the beginningProvide independenceDo not compare child’s progress to that of anyone elseProvide praise at every opportunityInstead of asking what something is, ask child to give it a name or tell you about itAllow choices where possible
  60. Q-U-E-S-TQUESTION the child’s parents and child too, if he is old enough to respondUSE appropriate pain assessmentEVALUATE the child’s behaviourSECURE the parent’s active participation in treatmentTAKE the cause of the pain into consideration
  61. – pictorial tool often used for preschool and young school-age childrenThe child looks at several pictures of faces ranging from happy to sad (0 to 5 scale) and then chooses whichever face reflects his or her pain
  62. Oucher Scale – pictorial pain assessment tool for 3-7 year old children 
  63. FLACC (Face, Legs, Activity, Cry and Consolability) – for infants and very young childrenBehavior is observed to assess painMeasures each of the five identified categories on a 0 to 2 scaleThe higher the total score, the more pain
  64. FLACC (Face, Legs, Activity, Cry and Consolability) – for infants and very young childrenBehavior is observed to assess painMeasures each of the five identified categories on a 0 to 2 scaleThe higher the total score, the more pain
  65. CRIES Neonatal Postoperative Pain Measurement ScaleCryingREQUIRES oxygen to maintain saturation about 95%Increased heart rate and blood pressureExpressionSleeplessnessNeonatal Infant Pain ScaleFacial ExpressionCryingBreathing patternsState of arousal Movement of arms and legsPremature Infant pain ProfileGestational ageHeart rateOxygen saturationBehavioral stateBrow bulgeEye squeezeNasolabialfurroq
  66. CRIES Neonatal Postoperative Pain Measurement ScaleCryingREQUIRES oxygen to maintain saturation about 95%Increased heart rate and blood pressureExpressionSleeplessnessNeonatal Infant Pain ScaleFacial ExpressionCryingBreathing patternsState of arousal Movement of arms and legsPremature Infant pain ProfileGestational ageHeart rateOxygen saturationBehavioral stateBrow bulgeEye squeezeNasolabial furrow
  67. CRIES Neonatal Postoperative Pain Measurement ScaleCryingREQUIRES oxygen to maintain saturation about 95%Increased heart rate and blood pressureExpressionSleeplessnessNeonatal Infant Pain ScaleFacial ExpressionCryingBreathing patternsState of arousal Movement of arms and legsPremature Infant pain ProfileGestational ageHeart rateOxygen saturationBehavioral stateBrow bulgeEye squeezeNasolabial furrow
  68. 1. INFANT: Facial expression is the most common and consistent behavioural response to all stimuli, painful or pleasurable and may be the single best indicator of pain for the provider and the parents. According to studies, it is more reliable than crying, HR or body position of movement. Mouth stretched openEyes tightly shutBrows and forehead knittedCheeks raised high enough2. Younger ChildrenNarrowing of the eyesGrimace or fearful appearanceFrequent and longer lasting bouts of crying with a tone that is higher and louder than normalLess receptiveness to comforting by parents or other caregivers Holding or protecting the painful areas
  69. PAIN Management:Pharmacologic interventionsAnticipate and prevent or minimize pain related to hospitalization, procedure and treatmentIdentify and relieve existing painNon pharmacologic interventions to reduce stress, increase comfort and enhance healing
  70. Pharmacologic Intervention – mainstay of pain management and it depends on the specific needs of the patientOpioid analgesics-Highly effective pain relievers and constitute the core of most pharmacologic interventions to manage acute pain in infants and children-Oral, sublingual, rectal, nasal, subcutaneous, transdermal, IV and intraspinal*Morphine (MS contin)*Fetanyl (Duragesic)
  71. Pharmacologic Intervention – mainstay of pain management and it depends on the specific needs of the patientOpioid analgesics-Highly effective pain relievers and constitute the core of most pharmacologic interventions to manage acute pain in infants and children-Oral, sublingual, rectal, nasal, subcutaneous, transdermal, IV and intraspinal*Morphine (MS contin)*Fetanyl (Duragesic)Non Opioid Analgesics-are prescribed to manage mild to moderate pain.-infants and children metabolize non opioid analgesics in the same manner and at the same rate as adult.*NSAIDS -relieve for mild to moderate pain and anti inflammatory effects -Ibuprofen (advil); Naproxen (Naprosyn); Tolmetin (Tolectin); Indomethacin (Indocin) & Ketorolac (Toradol) are approved for use in children -S.E: Inhibition of platelet aggregation and GI irritation*Acetaminophen -Is the DOC for treating mild pain. Available in suppository, liquid and table form. -it has the added benefit of helping reduce fever and is very safe, even for neonates. -long term can cause risk of liver damage
  72. Pharmacologic Intervention – mainstay of pain management and it depends on the specific needs of the patientOpioid analgesics-Highly effective pain relievers and constitute the core of most pharmacologic interventions to manage acute pain in infants and children-Oral, sublingual, rectal, nasal, subcutaneous, transdermal, IV and intraspinal*Morphine (MS contin)*Fetanyl (Duragesic)Non Opioid Analgesics-are prescribed to manage mild to moderate pain.-infants and children metabolize non opioid analgesics in the same manner and at the same rate as adult.*NSAIDS -relieve for mild to moderate pain and anti inflammatory effects -Ibuprofen (advil); Naproxen (Naprosyn); Tolmetin (Tolectin); Indomethacin (Indocin) & Ketorolac (Toradol) are approved for use in children -S.E: Inhibition of platelet aggregation and GI irritation*Acetaminophen -Is the DOC for treating mild pain. Available in suppository, liquid and table form. -it has the added benefit of helping reduce fever and is very safe, even for neonates. -long term can cause risk of liver damage
  73. Pharmacologic Intervention – mainstay of pain management and it depends on the specific needs of the patientOpioid analgesics-Highly effective pain relievers and constitute the core of most pharmacologic interventions to manage acute pain in infants and children-Oral, sublingual, rectal, nasal, subcutaneous, transdermal, IV and intraspinal*Morphine (MS contin)*Fetanyl (Duragesic)Non Opioid Analgesics-are prescribed to manage mild to moderate pain.-infants and children metabolize non opioid analgesics in the same manner and at the same rate as adult.*NSAIDS -relieve for mild to moderate pain and anti inflammatory effects -Ibuprofen (advil); Naproxen (Naprosyn); Tolmetin (Tolectin); Indomethacin (Indocin) & Ketorolac (Toradol) are approved for use in children -S.E: Inhibition of platelet aggregation and GI irritation*Acetaminophen -Is the DOC for treating mild pain. Available in suppository, liquid and table form. -it has the added benefit of helping reduce fever and is very safe, even for neonates. -long term can cause risk of liver damagePharmacologic InterventionsNonopioids and NSAIDs – mild to moderate pain; antipyretic effectsAcetaminophen and ibuprofenOpioids – sedation, mental confusion, constipation, pruritus, nausea, vomitingMorphine and FentanylMonitor vital signs after administering any analgesicsEMLA (Eutetic mixture of local anesthetics) – topical analgesicCombinationChildren (except infants younger than 3-6 months) – metabolize drugs more rapidly than adultsYounger children may require higher doses of opioids to achieve the same effect
  74. EMLA Cream (lidocaine 2.5% and prilocaine 2.5%), applied to intact skin under occlusive dressing, provides dermal analgesia by the release of lidocaine and prilocaine from the cream into the epidermal and dermal layers of the skin and by the accumulation of lidocaine and prilocaine in the vicinity of dermal pain receptors and nerve endings.  Lidocaine and prilocaine are amide-type local anesthetic agents.  Both lidocaine and prilocaine stabilize neuronal membranes by inhibiting the ionic fluxes required for the initiation and conduction of impulses, thereby effecting local anesthetic action.
  75. Complementary and alternative medicine (CAM)Complementary Pain MedicineMusic TherapyHypnosis – child’s concentration is focused, narrowed or absorbedTENS (transcutaneous electric nerve stimulation) unit – electric stimulation to relieve painAcupunctureNon-Pharmacologic CareComfort, positioning and non-nutritive suckingDistraction – method used to divert attention from the main portion of experience. Ex. Blowing bubblesRelaxation – tense and relax different muscle groupsGuided Imagery – use of pleasant mental images of events, feelings or sensations. Ex. Favorite vacation spotBiofeedback – training designed to help an individual control his or her autonomic nervous systemBehavioral Contracting
  76. Concept of Death in Childhood (Lippincotts William and Wilkins, 2005)Infancy. Concept of death – NONENursing considerations: Be aware that the older infant will experience separation anxietyHelp the family cope with death so they can be available to the infantEarly childhood. Knows the words “DEAD” and “DEATH”. Reactions are influenced by the attitude of the parents.Nursing considerations:Help the family members including siblings cope with their feelingsAllow the child to express his own feelings in an open and honest manner.Middle childhood. Understands universality and irreversibility of death. May have a fear of parents dying.Nursing considerationsUse play to facilitate the child’s understanding of deathAllow siblings to express their feelings.Late childhood. Beings to incorporate family and cultural beliefs about death. Explores views of an afterlife and faces the reality of own mortalityNursing considerationsProvide opportunities for the child to verbalize his fearsHelp the child discuss his concerns with the familyAdolescence. Adult perception of death, but still focused on the HERE and NOWNursing considerationsUse opportunities to open discussion about deathAllow expression of feelings of guilt, confusion and anxietySupport and maintain self esteem
  77. Concept of Death in Childhood (Lippincotts William and Wilkins, 2005)Infancy. Concept of death – NONENursing considerations: Be aware that the older infant will experience separation anxietyHelp the family cope with death so they can be available to the infantEarly childhood. Knows the words “DEAD” and “DEATH”. Reactions are influenced by the attitude of the parents.Nursing considerations:Help the family members including siblings cope with their feelingsAllow the child to express his own feelings in an open and honest manner.Middle childhood. Understands universality and irreversibility of death. May have a fear of parents dying.Nursing considerationsUse play to facilitate the child’s understanding of deathAllow siblings to express their feelings.Late childhood. Beings to incorporate family and cultural beliefs about death. Explores views of an afterlife and faces the reality of own mortalityNursing considerationsProvide opportunities for the child to verbalize his fearsHelp the child discuss his concerns with the familyAdolescence. Adult perception of death, but still focused on the HERE and NOWNursing considerationsUse opportunities to open discussion about deathAllow expression of feelings of guilt, confusion and anxietySupport and maintain self esteem
  78. Concept of Death in Childhood (Lippincotts William and Wilkins, 2005)Infancy. Concept of death – NONENursing considerations: Be aware that the older infant will experience separation anxietyHelp the family cope with death so they can be available to the infantEarly childhood. Knows the words “DEAD” and “DEATH”. Reactions are influenced by the attitude of the parents.Nursing considerations:Help the family members including siblings cope with their feelingsAllow the child to express his own feelings in an open and honest manner.Middle childhood. Understands universality and irreversibility of death. May have a fear of parents dying.Nursing considerationsUse play to facilitate the child’s understanding of deathAllow siblings to express their feelings.Late childhood. Beings to incorporate family and cultural beliefs about death. Explores views of an afterlife and faces the reality of own mortalityNursing considerationsProvide opportunities for the child to verbalize his fearsHelp the child discuss his concerns with the familyAdolescence. Adult perception of death, but still focused on the HERE and NOWNursing considerationsUse opportunities to open discussion about deathAllow expression of feelings of guilt, confusion and anxietySupport and maintain self esteem
  79. Concept of Death in Childhood (Lippincotts William and Wilkins, 2005)Infancy. Concept of death – NONENursing considerations: Be aware that the older infant will experience separation anxietyHelp the family cope with death so they can be available to the infantEarly childhood. Knows the words “DEAD” and “DEATH”. Reactions are influenced by the attitude of the parents.Nursing considerations:Help the family members including siblings cope with their feelingsAllow the child to express his own feelings in an open and honest manner.Middle childhood. Understands universality and irreversibility of death. May have a fear of parents dying.Nursing considerationsUse play to facilitate the child’s understanding of deathAllow siblings to express their feelings.Late childhood. Beings to incorporate family and cultural beliefs about death. Explores views of an afterlife and faces the reality of own mortalityNursing considerationsProvide opportunities for the child to verbalize his fearsHelp the child discuss his concerns with the familyAdolescence. Adult perception of death, but still focused on the HERE and NOWNursing considerationsUse opportunities to open discussion about deathAllow expression of feelings of guilt, confusion and anxietySupport and maintain self esteem
  80. Concept of Death in Childhood (Lippincotts William and Wilkins, 2005)Infancy. Concept of death – NONENursing considerations: Be aware that the older infant will experience separation anxietyHelp the family cope with death so they can be available to the infantEarly childhood. Knows the words “DEAD” and “DEATH”. Reactions are influenced by the attitude of the parents.Nursing considerations:Help the family members including siblings cope with their feelingsAllow the child to express his own feelings in an open and honest manner.Middle childhood. Understands universality and irreversibility of death. May have a fear of parents dying.Nursing considerationsUse play to facilitate the child’s understanding of deathAllow siblings to express their feelings.Late childhood. Beings to incorporate family and cultural beliefs about death. Explores views of an afterlife and faces the reality of own mortalityNursing considerationsProvide opportunities for the child to verbalize his fearsHelp the child discuss his concerns with the familyAdolescence. Adult perception of death, but still focused on the HERE and NOWNursing considerationsUse opportunities to open discussion about deathAllow expression of feelings of guilt, confusion and anxietySupport and maintain self esteem
  81. Helping parents to talk with their child about dying if he is ready to do soEncouraging all family members to express their feelings, even though they might be difficult to hearAllowing families to spend as much time as possible with the dying childAllowing and encouraging parents to continue to take an active role in their child’s careReminding parents that they don’t always have to be strong and ask for help
  82. Helping parents to talk with their child about dying if he is ready to do soEncouraging all family members to express their feelings, even though they might be difficult to hearAllowing families to spend as much time as possible with the dying childAllowing and encouraging parents to continue to take an active role in their child’s careReminding parents that they don’t always have to be strong and ask for help
  83. Thank you for Listening!