Inclusivity Essentials_ Creating Accessible Websites for Nonprofits .pdf
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.
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
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
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
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
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
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
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
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.
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.
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
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
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.
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
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
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
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
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
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
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
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
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.
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
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.
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.
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.
per rectum – increase danger of perforationPosition – avoid pressure on distended abdomenFacilitate observation
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.
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.
(higher than the normal range of 40-60 times per minute)
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
Jaundice –first 24 hours increase bili liver’s inability to conjugate excess biliAnemia – hemolysisHypogly – pancreatic hyperplasia
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
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
Amount exchanged and infused
3 representatives of chromosome 21 are present instead of the usual 2
Extra chromosome 21 trisomy 21-greater risk for older women - > 35 years of agePaternal age factor, 55 years of age or older
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
Lack shivering response produces heat through increased metabolic process
Warm items first – reduce heat loss
Head covering to prevent heat loss
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
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
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
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.
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
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.
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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.
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
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
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
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
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
Increases the perception of threatCan affect child's coping skillsGreatly depend on their age:
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
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
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
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
– 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
Oucher Scale – pictorial pain assessment tool for 3-7 year old children
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
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
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
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
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
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
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
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)
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
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
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
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.
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
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
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
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
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
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
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
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