NCM 209 Lec - Transes
NCM 209 Lec - Transes
birth or infection
MCN CONCEPT
12 DOH STANDARDS OF PRENATAL CARE
PRENATAL CARE
According to DOH, it is recommended before to
THE PURPOSE OF PRENATAL CARE IS TO have at least 4 visits, now, it should be at least 8
ENSURE AND UNCOMPLICATED PREGNANCY visits because statistics says…
AND THE DELIVERY OF A LIVE AND HEALTHY
INFANT Back in 2015, 303,000 pregnant women died, 2.7M
babies died, and 2.5M babies are pre-mature who
BALANCE OF FORCES IN PREGNANCY died.
3. Blood pressure
4. FHT
5. Fundic height
● use tape measure
A. start at the symphysis pubis to
fundus
➔ 5th month = 20 cm
➔ 6th month = 21-24 cm
➔ 7th month = 25-28 cm
➔ 8th month = 29-30 cm
➔ 9th month = 30-34 cm
6. Leopold’s maneuver
● Warm hands
➔ It is normally about 45% for men and ❖ Protein/albumin (for GDM) – PIH,
40% for women preeclampsia
❖ Mas mag take time ito kasi may ● It is a screening test not diagnostic test
fasting; 3 takes
● It only signals that further testing should be
❖ 75g Glucose done
❖ Dapat hutdon ang drink in 1 sitting! ● Most accurate during the 16th to 18th week
● Done late in the first trimester, @ 10th and ● absence of fetal blood
12th weeks. Or 15-20 wks
GASTROSCHISIS
● To check chromosomal defect, genetic
disorder especially if woman is 35 year old
and above ● a fetal complication of teratogens where fetal
abdominal cavity fails to close
❖ Down syndrome
❖ Neural tube defect ● represents a congenital defect characterized
by a defect in the anterior abdominal wall
● 8 – 10 weeks pa si placenta through which the abdominal contents freely
protrude
MATERNAL SERUM ALPHA-FETO PROTEIN
● abdomen did not close
● High levels of AFP = fetal neural defect:
❖ Anencephaly ● related factors:
★ infection (deprivation of oxygen) ➢ Genetic studies
★ young maternal age ➢ Rh incompatibility
★ Smoking ➢ Hydrops fetalis
★ drug abuse
★ low birth/gestational age (early labor ● Blood from the umbilical cord
= premature baby)
BIOPHYSICAL SCORING
SPINA BIFIDA
● 30 minutes observation by USD
SCORE INTERPRETATION
FETAL BREATHING
2 1 or more episodes of
active extension with
AMNIOTIC FLUID INDEX return to flexion of limbs
and trunk
● Anteroposterior diameter
● 4 quadrant technique
Note: if positive, there is an option to take the
FETAL MOVEMENT COUNTING
patient’s case; then do double gloving, soak
instrument separated from those with non-hep B ● done after 27 weeks AOG
patients; 30 mins:non for positive then it takes 1
hour for disinfection of instruments) ● (viable na man ang 28 weeks so justifiable
na dapat ganito na talaga ang number of
❖ Hepatitis B surface Antibodies (HBsAb) movement
● The test that looks for antibodies that ● twice daily for 20-30 minutes
your immune system makes in
response to the surface protein of the NORMAL = 5-6 movements in 20-30 minutes
hepatitis B virus,
RISK FACTORS CAUSING GDM: Increase level of glucose in the blood will cross the
placenta (macrosomic baby), so the baby will also
● Obesity (usually walang payat na diabetic) have hyperglycemia. And since the baby does not
have decreased sensitivity to insulin then it will have
● Family History
an increase in insulin, which will result to
● Personal History hyperinsulinemia. This will convert into growth
● Sedentary Lifestyle hormone which will result to big babies or
macrosomic babies. The increase level of glucose
● Improper Diet (sweet, salty and fatty foods) which will also increase the energy in cell
(adenotricosphate) that will lead to macrosomia.
PATHOPHYSIOLOGY OF GDM
FETAL/NEONATAL COMPLICATIONS OF GDM
Human Placental Lactogen
(Human Chorionic somatomammotropin) ● Fetal- naa sa sulod si baby (inside)
● Fetal hyperglycemia
Decrease Insulin sensitivity ● Fetal hyperinsulinemia
● Respiratory Distress
● Preeclampsia
● No diuretics 10 days before —> it can affect the ALCOHOL EFFECTS ON FETUS
result
● Fetal Alcohol Syndrome (FAS)
● At least 10 hours fasting —> there should be
a particular time in performing this to avoid
● Intrauterine Growth Restriction
delayed procedure
● Preterm Delivery
● Test is done in the morning OPIOIDS
● Morphine
● Heroin
● Methadone LIFETIME EFFECTS OF SUBSTANCE
ABUSE
● Analgesics (prescription is necessary for
pregnant women) ● Mental retardation
● Physical deformities (FAS)
STIMULANTS ● Developmental problems
IUGR or Intrauterine growth restriction
● Cocaine
● Amphetamine Gastroschisis is a factor for this
● Ecstasy
● Caffeine
ACQUIRED IMMUNODEFICIENCY
EFFECTS OF STIMULANTS SYNDROME (AIDS)
FICTION
HOW DOES HIV INTERRUPT THE
- It would be extremely unlikely to get HIV NORMAL FUNCTION OF THE IMMUNE
from kissing, even open-mouth deep kissing. SYSTEM?
HIV is transmitted through blood, semen,
vaginal fluids, and breast milks and these HIV INFECTED T-CELL
fluids are not usually present during kissing.
● HIV infects a type of white blood cell in the
6. Condoms are really effective in preventing
HIV transmission body’s immune system called a T-helper cell
(also called a CD4 cell).
FACT
● These vital cells keep us healthy by fighting
- Latex condoms have pores measuring off infections and diseases.
.5mm3, while HIV virus measures only
.005mm3. if the CD4 cells are low in amount, the person is
7. There is a connection between other STD’s
and HIV infection most likely susceptible to infection
- Having a sexually transmitted disease (STI) ● A measure of the number of helper T-cells
can increase a person’s risk of becoming
per cubic millimeter of blood, used to
infected with HIV up to 10x
analyze the prognosis of patients infected
with HIV. - the patient has to undergo frequent IV. ASYMPTOMATIC PERIOD
monitoring of CD4 cells
● Time period between seroconversion
● Number of CD4 cells in the blood provides a and onset of HIV/AIDS-related illness
measure of immune system damage ● Duration variable: < 1 year to > 15
years
● CD4 count reflects phase of disease
● Most people remain healthy
(asymptomatic) for about three years
CD4 count: this is where AIDS can be determined
● Duration may depend on
★ 500-1200: normal socio-economic factors
★ 200-500: beginning of HIV illness
● The CD4 count is above 500 cells/ml
★ <200: AIDS V.
PHASES OF HIV/AIDS
● Body starts making antibodies to HIV a few ★ Factors affecting the course of HIV/AIDS
include nutrition, emotional stress, and
weeks after infection access to health care
★ People infected with HIV can infect
● HIV test becomes positive
others at any phase of the disease
● Vaginal tears
● Antenatal care
BREASTFEEDING RECOMMENDATIONS ↓
↓
Increase Hemolysis
ANEMIA IN PREGNANCY
● Jaundice (discoloration/yellowish of skin)
Nutritional Influence of RBC Production
● Kernicterus (a medical term wherein ang
increase amount of bilirubin in the blood
will accumulate in the brain kay dili na ● Folic Acid
siya enough nga didto lang siya mag ● Vitamin B12 or cobalamin
stay ang bilirubin sa blood, maad na siya
kay ang blood maabot mana siya sa ● Iron
brain; if ang baby increase kaaayo ang
amount ng bilirubin sa brain would Increased Blood Volume 40-50% (Meet
experience seizure) increased demand, Protect from impaired
venous return, Prepare for blood loss) →
● Hydrops Fetalis (this is due to the
increase amount of bilirubin; a fetal Decrease hemoglobin concentration →
complication na magkaroon ng PHYSIOLOGIC ANEMIA
accumulation of fluid in the fetal
circulation) Signs and Symptoms of Anemia
↓ 3. Shortness of breath
4. Hypotension
● Erythroblastosis Fetalis (severe
hemolytic disease) (sobrang baba na ng 5. Asymptomatic
RBC; anemic na masyado ang baby)
Management of Physiologic Anemia
MANAGEMENT OF Rh INCOMPATIBILITY
● Intrauterine Fetal Blood transfusion (perform at ● Rest
28 weeks; guided by ultrasound) ● Iron supplement
● Replace fetal RBCs ● Oxygen therapy
● Keep the fetus healthy until he or she is ● Nutrition
mature enough to be delivered ● Blood transfusion- severe type of anemia
● Phototherapy
Priority Nursing Diagnosis of Anemia
★ Aka light therapy to treat jaundice
★ Exposure to light using ● Altered tissue perfusion
LED/polarized light at a specific time ● Altered Nutrition less than body
of the day requirements
● RhoGAM (very known medication) ● Activity intolerance
★ Anti D Immunoglobulin
★ After 28 weeks AOG Iron → Transferrin (stored by the stomach)
★ Within 72 hours after birth →Ferritin (absorbed by the intestine)
★ Suppress immune system of mother
not to produce antibodies (MOA)
● Bleeding
● Completion curettage
● Abdominal cramping
● Prophylactic antibiotic
● Passage of watery vaginal discharges
● Passage of product of conception o Anticipate for infections
● Oxytocin administration
(incomplete abortion)
Signs and Symptoms of Ectopic Pregnancy TUBAL PREGNANCY
● Symptoms of bleeding
● Bleeding into the uterine cavity: in the
implantation site kasi doon dadaan ang
blood kahit dito nag implant sa may fallopian
tube
● Sharp one-Sided abdominal pain: the area
where in the implantation happens
● Syncope or fainting: blood loss
● Referred shoulder pain (ruptured EP)
● tower abdominal pain
● Vaginal bleeding
● Abdominal tenderness
● Low HCG hormone
● Transvaginal ultrasound
● Physical examination: to perform head to toe
OVARIAN PREGNANCY
assessment
● Pregnancy test
● HCG: level of placental hormone
● Pelvic examinations: includes internal exam
FETAL MALPOSITION
MONITORING FETAL WELL-BEING
Persistent Occiput Posterior
-fetus enters the birth canal, descends, and is
• Early US for accurate gestational dating delivered in occiput posterior position.
• amniocentesis for fetal lung maturity -fetus is facing up instead of facing down the
• ultrasound if macrosomia is suspected vagina.
• antepartum newborn screening test post 34
weeks Transverse Occiput Arrest
-baby is head-down but the head is turned
PREGNANCY CATEGORY OF completely sideways towards the mother’s
MEDICATIONS: hipbone, causing baby to ‘arrest’ (get stuck)
because it doesn’t fit well.
Factors Causing POP
• Category A--safe (vitamins)
- lack of rotation due to poor contraction
• Category B-- no animal effects (penicillin)
-abnormal flexion of head
• Category C--no studies available
-incomplete rotation
• Category D--evidence of risk but benefits
-inadequate
outweigh the risks
-epidural anesthesia
• Category X-- risks outweigh benefits
-large baby
Surgical Management:
● Cesarean Section
NURSING MANAGEMENT:
● Hydration (Oral or IV)
● Bedrest (Home or Hospital), usually left side
lying
● Medications to stop labor (MgS04, brethine,
terbutaline, etc.)
ASSESSMENT:
● A complete pelvic examination is required,
including a rectovaginal examination to
assess sphincter tone
● A Sims speculum or a standard bivalve
speculum with the anterior blade removed
may facilitate diagnosis.
● Mild uterine prolapse may be recognized
only when the patient strains during the
bimanual examination
● Evaluate all patients for estrogen status.
UTERINE PROLAPSE ○ Signs of decreased estrogens
■ Loss of rugae in the vaginal
● Uterine Prolapse/Pelvic Relaxation/Pelvic mucosa
floor hernia ■ Decreased secretions
● a descent or herniation of the uterus into or ■ Thin perineal skin
beyond the vagina ■ Easy perineal tearing
● Considered under the broader heading of
“pelvic organ prolapse” which also include ● If urinary obstruction is present, the patient
cystocele, urethrocele, enterocele, and may exhibit suprapubic tenderness or a
rectocele tympanitic bladder.
● anatomically, the vaginal vault has 3 ● If infection is present, purulent cervical
compartments: discharge may be noted.
○ an anterior compartment
(consisting of the anterior vaginal
wall) Lab Studies Imaging Studies
○ a middle compartment (cervix)
● Laboratory ● Pelvic
○ posterior compartment (posterior
studies are ultrasound
vaginal wall).
unnecessary in examination
○ UP involves the middle compartment
uncomplicated ● Ultrasonograph
cases y
Four stages of uterine prolapse are defined:
● Cervical ● MRI- to grade
● stage I - descent of the uterus to any point
cultures - pelvic organ
in the vagina above the hymen
cases prolapse
● stage II - descent to the hymen
complicated by
● stage III - as descent beyond the hymen
ulceration or
● stage IV - total eversion or procidentia
purulent
discharge
Uterine prolapse always is accompanied by some
● Papanicolaou
degree of vaginal wall prolapse
test (Pap
smear
cytology) or
biopsy - rare
cases of
suspected
carcinoma
● BUN and
creatinine
measurement -
if PE findings
suggest urinary
obstruction
TREATMENT/MEDICAL MANAGEMENT:
● Pessaries
○ fitted into the vagina to hold the
uterus in place
○ Temporary or permanent form
○ fitted individually for each woman
○ Attaining and maintaining optimal
weight is recommended
● Surgery
○ uterus sutured back into place
○ colpopexy - involves the use of
surgical mesh for supporting the
uterus
○ Hysterectomy - removal of uterus
○ Provide factual information about
individual condition involved to
promote informed decision making
○ Provide for ways to obtain privacy to
allow for sexual expression for
individual and/or between partners
without embarrassment and/or
objection of others
● CONSTIPATION
○ Administer stool softeners/laxatives
as prescribed
○ Encourage increase in fluid and fiber
intake
○ Encourage early ambulation RISK FACTORS:
● Women who hace had previous surgery on
● URINARY INCONTINENCE the uterus (uupper muscular portion)
○ Determine if client is aware of ● Having more than five full-term pregnancies
incontinence. Developmental issus/ ● Having overdistended uterus (as with twins
medical conditions that can impair or other multiples)
patient’s awareness and sensory ● Abnormal positions of the baby such as
perception of voiding transverse lie
○ Determine patient’s particular ● Use of Pitocin (oxytocin) and other
symptoms (e.g continus dribbling) labor-induced medication (prostaglandin)
○ Implement bladder training for ● Rupture of the scar from a previous CS
incontinence management by delivery
providing ready access to bathroom ● Uterine/abdominal trauma
or commode, encouraging adequate ● Uterine congenital anomaly
fluid intake, and establishing ● Obstructed labor; maneuvers within the
voiding/bladder emptying uterus
● Interdelivery interval (time between
● SEXUAL DYSFUNCTION deliveries)
PATHOPHYSIOLOGY
ASSESSMENT:
● Evaluate maternal vital signs
● Note an increase in rate and depth of
respirations, an increase in pulse, or a drop
in BP indicating status change
● Assess fetal status by continuous monitoring
● Speak with family, and evaluate their
understanding of the situation
● Observe for signs and symptoms of
Impending rupture
○ Lack of cervical dilaition
○ Tetanic uterine contraction = nonstop
○ Restlessness
○ Anxiety
○ Severe abdominal pain
○ Fetal bradycardia
○ Late or variable deceleration of the
FHR
Oligohydra Maternal fear of ↑ Incidence of Fetal heart ↑ Fear for baby Tachycardia,
mnios “dry birth” congenital aberrations chronic asphyxic
anomalies ↑ Risk of insult, bradycardia,
cesarean birth, acute Asphyxic
↑ Incidence of renal forceps, vacuum insult Chronic
lesions Continuous hypoxia Congenital
electronic heart block
↑ Risk of IUGR monitoring and
intervention in
↑ Risk of fetal labor
acidosis
Uterine Hemorrhage Fetal anoxia
↑ Risk of cord rupture Cesarean birth
compression for hysterectomy Fetal hemorrhage
Postmaturity
↑ Risk of death ↑ Neonatal
Meconium ↑ Psychologic ↑ Risk of fetal morbidity and
staining of stress due to asphyxia mortality
amniotic fear for baby
fluid ↑ Risk of meconium
aspiration
↑ Risk of
pneumonia due to
PAGES 18-21
aspiration of
meconium
Postdates ↑ Anxiety Postmaturity
Premature ↑ Risk of ↑ Perinatal (>42 weeks) ↑ Incidence of syndrome
rupture of infection morbidity induction of ↑ Risk of
membranes (chorioamnio Prematurity labor fetal-neonatal
nitis) ↑ Incidence of mortality and
↑ Birth weight cesarean birth morbidity
↑ Risk of ↑ Use of ↑ Risk of
preterm labor ↑ Risk of respiratory technology to antepartum
distress syndrome monitor fetus fetal death
↑ Anxiety Fear Prolonged ↑ Risk of ↑ Incidence or
for the baby hospitalization shoulder risk of large
Prolonged dystocia baby
hospitalization
Diabetes ↑ Risk of ↑ Risk of
hydramnios malpresentatio Assessment Normal Abnormal
↑ Risk of n Technique Assessment Assessment
hypoglycemia ↑ Risk of Findings Findings
or macrosomia
hyperglycemia ↑ Risk of IUGR Inspection/ ● Exhaustion ● Extreme
↑ Risk of ↑ Risk of Observation ● Fatigue exhaustion
preeclampsia respiratory ● Sleep ,
eclampsia distress hunger weakness,
syndrome and
↑ Risk of depression
congenital at the end
anomalies of 6th
week
Preeclampsia - ↑ Risk of ↑ Risk of small ● Pallor
eclampsia seizures for-gestational- ● Anxiousne
↑ Risk of age baby ss and
stroke ↑ Risk of restlessne
↑ Risk of preterm birth ss
HELLP ↑ Risk of ● Dizziness
mortality ● Fainting
UTERINE ATONY
OVULATION AND
MENSTRUATION/LACTATION SIGNS AND SYMPTOMS
● Boggy Uterus
● Large Uterus
● Return of ovulation and menstruation varies ● Expulsion of large clots
for each postpartal woman ● Bright red bleeding
○ Menstruation returns between 6 and ● Hypovolemic shock
10 weeks after birth in nonlactating
mother - ovulation returns within 6 FACTORS CAUSING UTERINE ATONY
months ● Multiple Gestation
○ Return of ovulation and menstruation ● Hydramnios
in breastfeeding mother is prolonged ● Large baby
related to length of time ● Uterine Myoma
breastfeeding continues ● Anestheia
● Breast begin milk production ● Oxytoxic drugs
○ A result of interplay of maternal ● Multiparity
hormones ● Advanced maternal age
● Prolonged tocolytic agents
ASSESSMENT OF EPISIOTOMY/EPISSIORRAPY ● Dystocia
● Previous Uterine surgery
Assessment Normal Abnormal ● Chorioamnionitis
Technique ● Full bladder
LACERATIONS HEMATOMA
Vaginal: SIGNS AND SYMPTOMS OF HEMATOMA
● anterior ● severe perineal and pelvic pain not relieved
● posterior by analgesia
● lateral wall ● bluish bulging under the skin
Perineal: ● tenderness
● first degree – skin ● firm to palpate
● second degree – muscles ● minor bleeding
● third degree – external anal sphincter
● fourth degree – rectal sphincter and rectal FACTORS CAUSING HEMATOMA
mucus membrane ● Rapid Spontaneous birth
Cervical: ● Varicosities
● lateral ● Episiorrhaphy
● Lacerations
SIGNS AND SYMPTOMS OF LACERATIONS
● Firm and Contracted Uterus MANAGEMENT OF HEMATOMA:
● Bright red Bleeding MEDICAL MANAGEMENT
● Tear in the birth canal, and perineum ● Analgesics
● Cold Compress
FACTORS CAUSING LACERATIONS
● Precipitate labor SURGICAL MANAGEMENT
● Dystocia ● Incision and drainage
● Malpresentation ● Removal of sutures
● Large babies ● Packing
● Instrumentation ● Ligation of vessels
● Lithotomy position
● Rapid cervical dilatation NURSING DIAGNOSIS AND INTERVENTIONS
● Alteration in comfort; Pain ○ Administer oxygen as ordered
○ proper referral ● Dysfunctional Grieving
○ ice pack application on the perineum ● Anxiety Fear
○ analgesics as ordered ○ Obtain consent for surgery
○ assist for surgical intervention ○ Give factual informations
○ Explain procedures
○ Do not give reassurance o Emotional
support
UTERINE RUPTURE
COMPLETE
UTERINE INVERSION
● involves endometrium, myometrium and
perimetrium DEGREE OF INVERSION
● First-degree - the inverted fundus extends
INCOMPLETE to, but not through, the cervix.
● intact peritoneum ● Second-degree - the inverted fundus
extends through the cervix but remains
SIGNS AND SYMPTOMS OF UTERINE RUPTURE within the vagina.
● Localized abdominal pain ● Third-degree - the inverted fundus extends
● Abdominal tenderness outside the vagina.
● Tearing feeling ● Total inversion - the vagina and uterus are
● Hypovolemic shock inverted.
● Concealed bleeding
● Change in abdominal contour SIGNS AND SYMPTOMS
● Visualization of protruded uterus
FACTORS CAUSING UTERINE RUPTURE ● Sudden gush of large amount of blood
● Difficult Vaginal Delivery ● Hypovolemic shock after 10 minutes
● Weak uterine operative site
● vertical uterine scar from previous CS FACTORS CAUSING UTERINE INVERSION
● Faulty presentation ● Pulling the umbilical cord before placental
● Multiple gestation separation
● Traumatic maneuvers using instruments for ● Extreme pushing of the fundus
delivery ● Fundal implantation of the placenta
● Injudicious use of oxytoxic agents
● Obstructed Labor GOAL OF CARE OF UTERINE INVERSION
● Prevent Hemorrhage
GOAL OF MANAGEMENT OF UTERINE ● Jhonson’s Maneuver
RUPTURE ● Prevent Shock
● Repair of tear or laceration ● Prevent Infection
● Prevent Hemorrhage ● Prevent Death
● Prevent Hypovolemic shock
● Prevent Infection MEDICAL MANAGEMENT
● Prevent Death ● Initially:
○ Tocolytic
MEDICAL MANAGEMENT OF UTERINE ○ General anesthesia
RUPTURE ○ Nitroglycerine
● Intravenous fluid ● Oxytocic agents
● Blood Transfusion ● Double intravenous fluid
● Antibiotics ● Oxygen administration
● Oxytoxics ● Ready for CPR
● Antibiotics
SURGICAL MANAGEMENT OF UTERINE ● Blood Transfusion
RUPTURE
● Laparotomy SURGICAL MANAGEMENT
● Tubal ligation ● Jhonson’s Maneuver
● Hysterectomy ● Surgical Replacement
● Hysterectomy Laparotomy
NURSING DIAGNOSIS AND INTERVENTIONS OF ● General Anesthesia
UTERINE RUPTURE
● Fluid Volume Deficit NURSING DIAGNOSIS AND INTERVENTION
● Altered Cardiac Output ● Fluid Volume Deficit
● Altered Tissue Perfusion ● Altered Cardiac Output
○ Monitor VS every 15 minutes ● Altered Tissue Perfusion
○ Evaluate blood loss IVF and BT ○ Determine the degree of inversion
○ Assess VS, NVS, and CRT ● Retained Placenta fragments
○ Evaluate blood loss ● Endometritis
○ Use large needles/cannula for ● Uterine Myoma
intravenous fluid
○ Regulate IVF and BT as ordered MEDICAL MANAGEMENT OF UTERINE
○ Administer oxygen by face mask SUBINVOLUTION
● Anxiety ● Oxytocin
○ Emotional support ● M. Malate
○ Stay with the client ● IVF
○ Listen
○ Give factual informations SURGICAL MANAGEMENT OF UTERINE
● Risk for infection SUBINVOLUTION
○ Aseptic technique ● Hysterectomy
○ Administer prophylactic antibiotics
NURSING DIAGNOSIS AND MANAGEMENT
● Fluid
LATE POSTPARTUM HEMORRHAGE
● Volume Deficit
Occurs between 24 hrs and 6 weeks postpartum ● Altered Cardiac Outout
● Altered Tissue Perfusion
● Retained Placental Fragments ● Alteration in thermoregulation; hyperthermia
● Subinvolution – “Opposite of involution, ● AnxIety
Lumaki ang uterus even after panganak” ● Fear
● Endometritis
Gestational surrogates
- has no genetic ties to the child. That's
because it wasn't her egg that was used.
- more common than a traditional surrogate
OTHER REASONS:
- age
- sexual orientation
CHOOSING A SURROGATE:
1. Is at least 21 years old
2.
3. Has passed a psychological screening by a
mental health professional
4.
5. have a complete medical evaluation and
pregnancy history to assess the likelihood of a
healthy, full-term pregnancy.
implanted on the vaginal OS which causes
bleeding which can lead to preterm labor.
PEDIA Concept
● Placental Aging is due to the aging of the
placenta. Not enough nutrients are provided
HIGH RISK NEWBORN to the baby since the placenta is unable to
supply oxygen and nutrients to the baby
from the mother
PROBLEMS RELATED TO MATURITY: E. PREECLAMPSIA/ECLAMPSIA
PRETERM ● Increase blood pressure (hypertension)
during gestational age causes
vasoconstriction, which leads to decrease in
● Preterm is a neonate born before 37 weeks oxygen supply and nutrients to the baby,
of gestation which can cause prematurity.
○ 36 weeks and 6 days/7 is still
considered as preterm but, termed
as borderline preterm FETAL FACTORS
● Primary concern: relates to immaturity of all
body system A. MULTIPLE PREGNANCY
● Cause: unknown ● Most common factor
● Ex. twins, triplets, etc. which can be
MATERNAL FACTORS hereditary
● Uterine Stretch Theory – when a uterus
reaches its maximum capacity to stretch, it
A. AGE will initiate contraction which leads to
● The younger the mother, the more prematurity.
predispose to develop a preterm infant. ○ Ex. triplets: mas mudako ug maayo,
Example, teens aged 13-15 yrs old doesn’t ma reach ang maximum capacity to
have a fully developed body system to bear stretch so mag initiate ug contraction
a child maong madeliver ang babies even
● Mothers beyond 35 years old are not able to though preterm pa..
bear a baby due to their body system not
being normal which can most likely cause a B. INFECTION
premature baby ● Presence of infection warrants prematurity
● Once the baby has an infection, the fetus
experiences respiratory distress so the baby
has to be delivered, which can cause
prematurity
● The baby can still be delivered normally
depending on its condition and if the baby
responds to the meds
OTHOTHER FACTORS
● Neonate born after 42 weeks of gestation 2. The failing placental function will place infant
● About 12% of all infants are post-term at risk for intrauterine hypoxia during labor
● Causes of delayed birth is unknown and delivery.
● Hypoxia – respiratory distress Fig 7.
Post term baby
MATERNAL FACTORS
● If the baby is experiencing distress, it
facilitates relaxation of rectal
A. First pregnancies between the ages 15 to muscles, which releases meconium.
19 years are unexpected pregnancies, they Meconium then floats around the
tend to hide their pregnancies. amniotic sac which the baby can
○ As a result, dili iingon na nag labor or drink which would lead to meconium
start na ang labor so ma extend ang aspiration syndrome once the baby is
labor delivered.
B. Woman older than 35 years
C. Multiparity with small babies so dili mafeel so 3. MECONIUM ASPIRATION SYNDROME
the uterine won’t reach its maximum capacity ● Crying is a baby’s first reaction. If the
which can lead to post term babies. baby swallowed its meconium, matuk
an ang baby then ang meconium
pwede muadto sa lungs.
FETAL FACTORS
4. HYPOGLYCEMIA - from nutritional
deprivation and poor storage of glycogen at
A. Fetal anomalies such as anencephaly birth
● Anencephaly – baby’s brain didn’t develop. ● Placental aging – decrease oxygen,
Life can be sustained but can’t live longer. nutrients which would lead to low
Death depends on the severity (most blood glucose, resulting in lethargy
common is 3 hours)
5. POLYCYTHEMIA- increase RBC (from both
mother and baby)
ASSESSMENT ● Manifestation: reddish
NURSING INTERVENTIONS
1. Observe for signs of respiratory distress
ASSESSMENT
● Respiratory distress MATERNAL FACTOR
○ SGA associated with prematurity
● Loose and dry skin, little fat, little muscle mass ● Maternal DM – the most widely known
● Wasted Appearance (payat) contributing factor, increase insulin acts as a
● Small liver fetal growth hormone
● Head is larger compared to body ● The baby is inside the mother with Diabetes
● Wide skull sutures Mellitus
● Poor skin turgor ● Maraming sugar sa loob ng mother so the
● Sunken abdomen doctor prescribed her with synthetic insulin
○ Decrease abdominal muscle ● Glucose goes inside the baby’s body since it is
a nutrient and it’s able to pass through the
placental barrier
● The baby then produces its own insulin to
compensate sa daghan na glucose na
makuha ni baby from mommy.
○ Insulin from the mother cannot pass
through the placental barrier since
malaki ang molecule ng insulin
● Since sige produce and baby ng insulin,
managhan na ang insulin
○ Aside sa pang store ug glucose, fetal
growth hormone din ang insulin
maong mudako ang baby
● Once ma cut ang cord after delivery, pa cut din
ang glucose supply pero maretain parin ang
glucose na naa na sa body ng baby
● It would take time for the baby’s body to adjust
na hinayan na ang pag produce ng insulin
○ Mag decrease ang blood glucose
levels ni baby since na cut off naman
iyang supply, as a result mas daghan
na ang insulin compared sa glucose,
which causes hypoglycemia
FETAL FACTORS
● Increase insulin acts as a fetal growth
hormone - Hypoglycemia
● Macromia - an unusual large newborn with a
birth weight more than 4500 grams or 4kgs
ASSESSMENT
● Large, obese
● Lethargic and limp = hypoglycemia
● May feed properly because of lethargy
● Signs and symptoms of birth trauma (if NSVD)
○ Bruising
○ Broken clavicle
■ Pelvic disproportion (mother’s PROBLEMS OF LGA BABIES
pelvic is proportion but since 1. Hypoglycemia (low blood sugar) of baby after
the baby is too big and the delivery
shoulder is broader, doctors 2. Respiratory distress
intentionally break the clavicle ● Due to prolonged labor
in order to deliver the baby. 3. Hyperbilirubinemia
○ Evidence of molding ● Increase bilirubin level
■ Resulting from pressure on 4. Potential complications related to increase in
the baby’s head during body size:
childbirth ● Leading cause of breech position and
○ Cephalhematoma shoulder dystocia
■ Presence of blood clots, ● Fractured skull, clavicles, cervical or brachial
accumulation of blood plexus injury, and Erb’s palsy
○ Caput succedaneum ○ Shoulder dystocia – difficulty
■ Cranial trauma delivering the shoulder
○ Erb’s palsy – naipit ang part ng facial
nerves •
● Generally, there is no treatment other than
lifting the child gently to prevent discomfort.
Occasionally, the arm on the affected side
may be immobilized (movement is restricted
by applying restraints)
COMMON ACUTE CONDITIONS OF NEWBORN
MANAGEMENT
A. OXYGEN THERAPY
● Hood nasal prong, mask, endotracheal tube,
CPAP (Continuous positive airway pressure)
or PEEP (Positive and expiratory pressure)
may be used)
HYPERBILIRUBINEMIA
c) Infections
● is an abnormally high level of Bilirubin in the d) Birth trauma
blood; results to jaundiced e) Maternal diabetes
○ RBC starts to breakdown (hemi into f) Medications
globin). Globin is further broken ● There are certain medications that can lead
down which results to bilirubin and to conjugation of bilirubin
needs to be conjugated. Additional Notes:
○ Unconjugated bilirubin in the liver ● Mixing of maternal and fetal blood happens
results as a waste product during delivery
○ Conjugated bilirubin becomes ○ Placenta is detached from the
water soluble which gives color to the abdominal wall resulting in small
urine and stool openings or wounds on the wall =
● In physiologic jaundiced: mixing of maternal and fetal blood
○ occurs on the second day to seventh
day (sometimes extends to 10 days) ● No mixing of maternal and fetal blood
○ average increase of 2mg/dl; not during the pregnancy
exceeding 12mg/dl ○ Placenta is attached on the
● Pathological Jaundice of Neonates abdominal wall. Oxygen, nutrients,
○ Any of the following features etc. are transferred from the mother
characterizes pathological jaundice: and baby through Facilitated
■ Clinical jaundice appearing in Diffusion and Active Transport.
the first 24 hours.
■ Increases in the level of total
bilirubin by more than 12
ASSESSMENT
mg/dl
● Therapy is aimed at preventing Kernicterus,
which results in permanent neurological
damage resulting from the deposition of
bilirubin in the brain cells.
CAUSES
a) Immaturity of the liver
● Cannot facilitate bilirubin conjugation
b) Rh or ABO incompatibility
● Blood factors
ABO Rh
MANAGEMENT
1) Phototherapy (Bililight)
● is use of intense florescent lights to reduce
serum bilirubin levels
● The use of blue lights overhead or in blanket 2) Exchange blood transfusion via umbilical
– device wrapped around infant catheter-for very severe cases
● Injury from treatment, such as: eye damage, ● infants blood – remove = 5 / 10ml at a time
dehydration, or sensory deprivation ● infused with PlainNSS
○ Eye damage – too much exposure to ● draw blood from artery, infuse blood in the
UV light; provide eye shield to vein
prevent eye damage
○ Dehydration – init ang light
○ Sensory deprivation – baby isn’t
carried if it is undergoing
phototherapy
● Possible complication of phototherapy: eye
damage, dehydration, sensory deprivation
● Wallaby blanket - a blanket which, when
wrapped around the infant’s torso, delivers
effective therapy to jaundiced babies
○ no need to cover the baby’s eyes as
all light treatment is delivered
through the blanket NURSING INTERVENTIONS
● Physiologic jaundice can disappear if the
1. Expose as much of the newborn's skin as
baby is exposed to sunlight because of the
possible.
UV rays
● Undress the baby
2. Cover the genital area, and monitor the
genital area for skin irritation or breakdown.
● Do not remove the diaper
3. Cover the newborn's eyes with eye shields
or patches; make sure that eyelids are closed
when shields or patches are applied.
4. Remove the shields or patches at least
once per shift (during a feeding time) to
inspect the eyes for infection or irritation and
to allow eye contact and bonding with parents.
5. Monitor skin temperature closely.
● Body temp increases because of
exposure to light Ioff if init na kaayo
si baby
6. Increase fluids to compensate for water loss
○ Increase fluid through IVF Letting
the baby drink water can lead to
water intoxication.
○ Increase fluid through IVF Letting
the baby drink water can lead to
water intoxication
7. Expect loose green stools and green urine
8. Monitor the newborn's skin color with the
fluorescent light turned off, every 4 to 8 hours.
● Check for progress
9. Monitor the skin for bronze baby syndrome
- a grayish-brown discoloration of the skin.
● Too much exposure
● Continuous phototherapy – not ● Rh: mother (-) – pinoy, father (usually
turned off for 24 hours. Only turned +) – foreigner = expect
off if diaper needs to be changed or hyperbilirubinemia
for feeding. (more severe = longer 20. Prepare for phototherapy, and monitor the
exposure) newborn closely during the treatment
● Intermittent phototherapy – has a
schedule. Usual order is 6 hours on
and 6 hours off (ex. 7am on, 1pm off,
7pm on, 1am off)
10. Reposition newborn every 2 hours.
● Provide ample time for exposure
● Prevent ulceration
11. Provide stimulation.
12. After treatment, continue monitoring for
signs of hyperbilirubinemia, because
rebound elevations are normal after therapy is
discontinued.
13. Turn off phototherapy lights before
drawing blood specimen for serum bilirubin
levels and avoid allowing blood specimen to
remain uncovered under fluorescent lights (to
prevent the breakdown of bilirubin in the
blood specimen).
● Blood specimen exposed under the
light gives a false result. Cannot get
actual serum bilirubin level since the
blood is exposed under the light so
mag continue ug breakdown
14. Monitor for the presence of jaundice;
assess skin and sclera for jaundice
● Assessment is crucial within the first
24 hours MECONIUM ASPIRATION SYNDROME (MAS)
● Apply blanch pressure then slowly ● Occurs when infants take meconium into their
release. When you are going to lungs during or before delivery
blanch, the skin turns white and ● Occurs in term or post-term infants
slowly turns to pink after you release. ● During fetal distress there is increases
If jaundice is present, the skin slowly intestinal peristalsis, relaxing the anal
turns to yellow once you release sphincter and releasing meconium into the
pressure. amniotic fluid.
● The more severe, the more it will ● Aspiration can occur in utero or with the first
appear on the eyes breath.
● Dark skin – check inner arm, sclera, ● Meconium can block the airway partially or
or inner lip completely and can irritate the newborn’
15. Examine the newborn's skin color in natural airway, causing respiratory distress
light.
16. Press finger over a bony prominence or tip
of the newborn's nose to press out capillary CAUSES AND RISK FACTORS
blood from the tissues. 1. Common to post mature
● Jaundice starts at the head first, 2. Maternal history of diabetes
spreads to the chest, abdomen, and 3. Hypertension
then the arms and legs, followed by 4. Difficult delivery
the hands and feet 5. Poor intrauterine growth
● Checking severity of jaundice
17. Keep newborn well hydrated to maintain
blood volume.
● IVF flow rate should correct ASSESSMENT
18. Facilitate early, frequent feeding to hasten Respiratory distress is present at birth:
passage of meconium and encourage ● tachypnea,
excretion of bilirubin ● cyanosis,
19. Report to the physician any signs of ○ ineffective breathing pattern can lead
jaundice in the first 24 hours of life and any to
abnormal S&S ○ ineffective oxygenation that can lead
to hypoxia which leads to cyanosis
● retractions, ruptures, the baby is already exposed which
○ due to the effort of the baby’s puts the baby at risk for infection
breathing pattern 2. Prolonged or difficult labor
○ subcoastal or substernal ● can develop ascending infection because of
● nasal flaring, internal examination
● grunting, 3. Maternal infection
● Crackles, and rhonchi may be present. ● Once the mother is sick, it can be passed on
● Infant’s nails, skin, and umbilical cord may to the baby, especially during the 3rd
be stained a yellow-green color. trimester
4. Cross contamination
5. Aspiration
● Aspiration of meconium
● Aspiration of milk
● Aspiration pneumonia – when food, saliva,
liquids, etc. is breathed into the lungs. Since
these are foreign bodies, it could put the
baby at risk for infection
ASSESSMENT FINDINGS
Often does not have specific sign of illness
1. Poor feeding
MANAGEMENT ● most common problem assessed if the
a) Suctioning must be done immediately after patient is experiencing sepsis
the head is delivered before the first breath 2. Irritability
is taken; 3. Lethargy
● No need to suction if amniotic fluid is 4. Pallor
clear because there is no meconium 5. Tachypnea
staining 6. Tachycardia
b) Vocal cords should be viewed to see if the 7. Abdominal distention
airway is clear before stimulation and crying ● Assessed by getting abdominal girth
● Extracorporeal membrane 8. Temperature instability - difficulty keeping
oxygenation (ECMO)- temperature within normal range
● Cardiopulmonary bypass to support
gas exchange allows the lungs to DIAGNOSIS
rest
1. Blood culture, urine culture, and
cerebrospinal fluid cultures
NURSING INTERVENTIONS 2. Routine CBC, urinalysis, fecalysis
1. No need to suction if amniotic fluid is clear 3. Radiographic test
because there is no meconium staining Additional Notes:
● Monitor vital signs ● Urinalysis – determine if there is infection
2. Ensuring adequate oxygenation but cannot determine the type of bacteria
3. Administration of antibiotic therapy ● Urine Culture - dili pwede mag diretso
● Given immediately; don’t wait for signs of unless sure na naa nay infection. Urine
infection = prophylaxis (prevention) culture determine the type of bacteria
4. Maintain thermoregulation present in urine
○ To be certain what causes the
infection
● Urine culture and sensitivity - test the type of
SEPSIS bacteria that is sensitive in a particular
● Generalized infection resulting from the medication
presence of bacteria in the blood
● Major common cause is group B beta- MANAGEMENT
hemolytic streptococci
1. Intensive antibiotic therapy
● Depending on the type of bacteria present
CONTRIBUTING FACTORS (common: Amoxicillin, gentamicin, amikacin)
1. Prolonged rupture of membranes 2. IV fluids
● Amniotic sac serves as a shield to protect 3. Respiratory therapy
the baby from infection. Once the membrane ● includes oxygenation, percussion, vibration
(help loosen secretions)
NURSING INTERVENTIONS FETAL CIRCULATION
Routine newborn care with special emphasis on the
following:
E. VALVULAR DEFECTS
a) right side – tricuspid (separates R & L
ventricle)
b) left side – mitral / biscuspid
● S/S: palpitations
D. COARCTATION OF AORTA ○ once blood enters into a certain
chamber, the valve should close.
● Narrowing of the aorta Since sira ang tricuspid valve, mag
● Significant decrease in blood flow to abdomen flutter siya = palpitations
and legs ○ Pain
○ Decrease in blood flow because of ○ Edema
the narrowing ■ Sobra congest
● Blood shunted to head and arms ○ Weakness, dizziness
● S/S: BP /pulse – higher in arms than legs ■ Kulang ang oxygenated blood
○ High pulse pressure in carotid and to be distributed to other parts
radial pulse of the body
■ Bounding carotid and radial ● Mgt: Surgery – valvotomy, valvuloplasty
pulse valve replacement
○ Warm upper body ○ Valvotomy – repair
■ More blood ○ Valvuloplasty – replace (usually pig)
○ Cold and clammy lower extremities
due to compromised blood flow
● Mgt: surgery – angioplasty – repaired of
narrowed vessel
Additional Notes:
● Coarctation of the aorta refers to a
narrowing of the main blood vessel carrying
oxygen-rich blood from the heart to the body
throughout the body maong kulang ang
CYANOTIC TYPE
oyxgen
A. TRANSPOSITION OF GREAT VESSELS ● Pulmonary artery and aorta are switched from
their normal positions
● Aorta arises from right ventricle, pulmonary ● Deoxygenated bloods goes to the body
artery arises from left ventricle oxygenated instead of the lungs.
blood therefore circulates through left side of ● Oxygenated blood returns from the lungs and
heart to lungs and back to left side goes right back to the lungs again instead of
● Unoxygenated blood enters the right atrium to the body
from body, goes back to right ventricle and ● Mustard operation – corrects the problem by
back to circulation without being oxygenated using a synthetic material creating baffles to
● S/S: direct deoxygenated blood to the lungs and
○ Cyanotic appearance oxygenated blood to the body.
○ Shortness of breath
○ Poor feeding
○ Clubbing of the fingers or toes – B. TETRALOGY OF FALLOT
very evident manifestation of heart ● This condition is characterized by the following
problems four defects:
○ peripheral hypoxemia - ex. cold, ○ Ventricular Septal Defect - an
clammy skin, slow pulse abnormal opening, or ventricular
○ Severe progressive pulmonary septal defect, that allows blood to
hypertension. pass from the right ventricle to the
● Complications: left ventricle without going through
○ Arrythmias the lungs
○ Heart failure ○ Pulmonary Stenosis - a narrowing
● Mgt: Balloon Atrial Septostomy (Rashkind (stenosis) at or just beneath the
Procedure) pulmonary valve that partially blocks
the flow of blood from the right side
of the heart to the lungs
○ Right Ventricular Hypertrophy - the
right ventricle is more muscular
than normal
■ Since nag narrow ang
pulmonary valve, mas
maraming blood maiwan sa
right ventricle
■ Compensatory mechanism:
mag expand
○ Overriding Aorta - the aorta lies
directly over the ventricular septal
defect
■ Blood from the right ventricle
and left ventricle goes to the
aorta
● Tetralogy of Fallot results in cyanosis (bluish
color of the skin and mucous membranes due
to lack of oxygen)
Additional Notes: ○ There is lack of oxygen because
● Override between the two great vessel: deoxygenated blood didn’t go to the
Pulmonary artery & Aorta lungs which was supposed to be
● Normal: Pulmonary artery is connected oxygenated by the lungs
directly to distribute deoxygenated blood to ● Cyanosis develops within the first few years of
the lungs life.
● Normal: Aorta receives blood coming from the ● First presentation may include poor feeding,
left ventricle to distribute to the body fussiness, tachypnea, and agitation
● Transposition: pulmonary artery is directly ○ Poor feeding – lack of oxygen
connected to the aorta. Deoxygenated blood because feeding entails oxygenation
directly goes into the circulation without going ● Cyanosis occurs and demands surgical repair.
through the lungs ● Dyspnea on exertion is common.
● Ang deoxygenated blood sa pulmonary artery ● Hypoxic "tet" spells are potentially lethal,
kay niadto sa aorta na dapat sa lungs. Since unpredictable episodes that occur even in
niadto man sa aorta, ma dispense ang blood noncyanotic patients with TOF. These spells
can be aborted with relatively simple
procedures
○ Mukalit lang lagom ang bata
● Birth weight is low.
● Growth is retarded.
● Development and puberty may be delayed.
● Right ventricular predominance on palpation
● May have a bulging left hemithorax
● Systolic thrill at the lower left sternal border
● Single S2 - Pulmonic valve closure not heard
● Systolic ejection murmur
● Cyanosis and clubbing – Variable
● Squatting position
○ Facilitate return of blood going to the
circulation
● Scoliosis
○ Common associated problem with
TOF
● Retinal engorgement
○ More blood going to the upper
extremities
● Hemoptysis
○ Coughing out blood
○ Ma irritate and bronchial artery since
kulang ang oxygen sa lungs. Once
ma irritate, it causes blood and once
mag ubo, ma spit out ang blood
● Mgt: Tet Spells
○ Knee-chest position:- This provides a
calming effect, reduces systemic
venous return.
○ Oxygen therapy
○ Morphine sulfate - decrease systemic
venous return.
○ Surgery: Blalock Taussig Shun
A thorough history is the best guide to establishing
the etiology of the failure to thrive:
HIGH RISK INFANT
● Poverty is the greatest single risk
factor worldwide and in the United
COMMON HEALTH PROBLEMS DURING States
INFANCY ● Nutritional deficiency is the
fundamental cause
MENINGITIS
● inflammation of meninges of the brain and ● Opisthotonos - arching of the back head
spinal cord and heels bent backward and body arched
● Cause by bacteria, viruses, other forward
microorganism
● as a primary disease or as a result of
complications of neurosurgery, trauma,
infection of the sinus or ears, or systemic
infections.
● H Influenzae Meningitis
○ the most common form; between 6 to
12 months
○ Bacterial meningitis - Haemophilus
influenza type B, Streptococcus
pneumoniae, or Neisseria ● Brudzinski sign - Flexion at the hip in
meningitidis response to forward flexion of the neck
○ Viral meningitis is associated with
viruses such as mumps, herpesvirus,
and enterovirus.
Diagnosis
- CSF testing obtained by lumbar puncture
- The fluid is cloudy with increased pressure,
increased white blood cell count and
elevated protein and decreased glucose
levels
Interventions:
1. Provide isolation and maintain it for at least
24 hours after antibiotics are initiated.
2. Administer antibiotics and antipyretics as
prescribed.
3. Perform neurological assessment and
monitor for seizures and complications
4. Assess for changes in level of
consciousness and irritability
5. Monitor intake and output
LUMBAR TAP 6. Assess nutritional status.
7. Determine close contacts of the child with
meningitis because the contacts will need
Assessment prophylactic treatment
● Fever, chills, headache, 8. Meningococcal vaccine is recommended to
● high-pitched cry, irritability protect against meningitis
● Vomiting, Poor feeding or anorexia
and return to baseline
condition
SEIZURES
- Pahumanay na
● Recurrent sudden changes in b. Absence - rarely 20 seconds, stares
consciousness, behavior, sensations and or straight, does not fall
muscular activities beyond voluntary control
cause by excess neuronal discharge ➢ Status Epilepticus - continuous seizure,
● Normally the neuron sends out messages in cause by a tumor or blockage
electrical impulses periodically and the firing
individual neuron is regulated by an Contributing Factors (Seizure Disorder)
inhibitory feedback loop mechanism 1. Intracranial infection - common in meningitis
● With seizures many more neurons than or hydrocephalus
normal fire in a synchronous fashion in a 2. Space occupying lesion
particular area of the brain; the energy 3. CNS defects
generated overcomes the inhibitory
feedback mechanism Assessment Findings
1. Restlessness/irritability
2. Body stiffens and loss of consciousness
Febrile Seizures 3. Clonic movements - quick, jerking
movements of arms, legs, and facial muscle
● Common in children between 6 mos – 3 yrs 4. Pupils dilate and roll up
old
● Common in 5% of population under 5 years Treatment
old, familial 1. Drug Therapy
○ *familial = if a member in the family a. Diazepam
has a history of disease, the offspring b. Phenobarbital
may manifest the disease *threshold c. Dilantin
varies between patients, some pt.
may have a seizure triggered by a 2. Surgery
temp. of 39.1 C a. Tumor
● Non Progressive, does not generally result b. Hematoma
in brain damage
● Commonly associated with high fever – 38.9 Diagnostic Test
to 41.1 Celsius ● Blood studies
● Some appear to have a low seizure ○ to rule out lead poisoning,
threshold and convulse when a fever of 37.8 ○ Hypoglycemia
to 39.8 ○ Infection
○ Electrolytes imbalance
Classification
1. Partial Seizure ● EEG – to detect abnormal wave
- - Putting nodes to check brain activity
a. Simple - localized motor activity,
shaking of arm or leg, limited to one Interventions
side of the body 1. Reduce fever with antipyretics.
2. Give prescribed medication
b. Complex - psychomotor seizure, 3. Generalized seizure precautions
memory loss and staring, non 4. Do not restrain; pad crib rails; do not use
purposeful movements tongue blade
5. Observe and record the time of seizure,
➢ AURA – sensation that signals an attack duration, and body parts involved.
➢ After – sleep or confuse; unaware of the 6. Suction and administer oxygen after the
seizure seizure as required.
7. Observe the degree of consciousness and
2. Generalized behavior after seizure
a. Tonic - Clonic 8. Provide rest after the seizure
➢ Prodromal - maluya; early
symptoms Seizure Precautions
➢ AURA - naay makita na lights ● Keep the head elevated
and other feels na murag ● Oxygen on standby - hook pt. During
padulungay na mag seizure seizure, do not give via nasal cannula above
➢ Tonic - bubbles in the mouth 4L of O2
➢ Post ictal - occurring between ● Medication located at nurse’s station
the end of an epileptic seizure
● Take note of the time of the seizure and ● Administration of the prescribed
when it ends antibiotics, emphasizing that the 10-
● Suction equipment on standby at bedside in to 14-day period is necessary to
case of choking eradicate infective organisms.
● Screening for hearing loss may be
necessary.
OTITIS MEDIA
● Administering ear medications.
● Bacterial or viral infection of the middle ear ○ Younger than age 3, pull the
● Common in infants and preschoolers lobe down and back.
● Eustachian is shorter, wider, and straighter ○ Older than 3 years, pull the
thereby, allowing nasopharyngeal secretion pinna up and back.
to enter middle ear more easily
CLEFT LIP AND PALATE
Assessment Findings
1. Behavior that would indicate pain ● Non-union of the tissue and bone of the
- restless and repeatedly shakes the upper lip and hard/soft palate during
head embryonic development
- frequently pulls or tugs at affected ● Failure of the maxillary and premaxillary
ear processes to fuse during fetal development
2. Irritability, cough, nasal congestion, fever
3. Hearing impairment Etiology - primarily genetic environmental factors
4. Purulent discharges ● Viral infection
● Exposure to radiation
Diagnosis ● Folic acid deficiency
1. Examination of ear with otoscope ● Teratogenic factors
- reveals bright red bulging eardrum
2. Culture and sensitivity of ear discharges Assessment Findings
1. Facial abnormality
Possible Complication 2. Difficulty sucking and swallowing
- permanent hearing loss 3. Milk escapes through nose
- mastoiditis - inflamed mastoid, bacteria
migrates to area
Management
1. Antibiotics, analgesics
2. Myringotomy
- Incision into the tympanic membrane
to relieve pressure and drain the fluid
with/without tube
Post-operative Interventions
1. Wear earplugs while bathing, shampooing,
and swimming,
2. Diving and submerging under water are not
allowed.
3. Child should not blow his or her nose for 7 to
10 days after surgery
Assessment
Interventions ● Cleft lip
1. Encourage fluid intake. ○ can range from a slight notch to a
2. Teach the parents to feed infants in upright complete separation from the floor of
position, to prevent reflux. the nose
3. Instruct the child to avoid chewing as much ● Cleft palate
as possible during the acute period because ○ nasal distortion
chewing increases pain. ○ midline or bilateral cleft
4. Provide local heat and have the child lie with ○ variable extension from the uvula
the affected ear down. and soft and hard palate.
5. Instruct the parents in the appropriate
procedure to clean drainage from the ear Associated problems
with sterile cotton swabs. 1. .Feeding problems
6. Instruct the parents in: 2. URTI - milk may enter the lungs if inhaled
● Administration of analgesics or 3. Ear infection
antipyretics 4. Speech defect, dental malformation
5. Body image stomach
Management (Rule of ten) Gastrostomy – creation
1. Surgical Correction of an opening directly
● Cheiloplasty - Corrections of cleft into the stomach
lip, done - 2 months old
● Palatoplasty - Cleft palate surgery Fig. 23 Client who
○ Done - before speech underwent gastrostomy
development
○ Allow for palatal changes that Gastrostomy
take place with in 12-18 tube
months Create a balloon
● Logan bar/steri strips - to take the to anchor; para
tension off the sutures dili matanggal
For the food
Con’t Management (OF)
2. Team approach therapy Stoma
● Dentist and orthodontist
● Audiologist Stricture – narrowing of the area because of the
● Speech therapist scarring from the infection
● Pediatrician
NURSING INTERVENTION PRE OPERATIVE-
Nursing Intervention (PRE OP CLEFT LIP) LEFT CLEFT PALATE
1. Feed in upright position’ in small frequent ● Prepare parents to care for child after
feedings surgery
2. Burp frequently - feeding lasting 5 - 10 min. ● Instruct concerning feeding methods and
Then immediately burp positioning
3. Use large-holed nipples ○ Feed upright, use large-holed nipples
4. Use rubber-tipped syringe – if unable to suck
5. Gavage feeding as ordered NURSING INTERVENTION POST
6. Finish feeding with water OPERATIVE-LEFT CLEFT
7. Provide emotional support for parents and ● Suction mucus and saliva gently and do not
family touch the sutures
● Incision care
Nursing Intervention (POST OP CLEFT LIP) ● Clean suture with sterile cotton swab with
1. Maintain patent airway half strength hydrogen peroxide followed by
2. Assess color; monitor for frequent saline
swallowing ● Apply antibiotic ointment
3. Do not place in prone position ● Do not displace logan bar
4. Avoid straining suture lines ● Do not place in prone position, place in side
5. Use elbow restraints - prevent scratching the lying position
site with hands ● Keep spoons, pacifier, straws, away from
6. Resume feedings as ordered (Haberman child’s mouth for 7-10 days post op
feeder) ● Elbow restrain
7. Provide pain control as ordered ● Special feeder - syringe with rubber tubing
into side of mouth, breck feeder
Additional Notes: ● Monitor respiratory status.
✓ Death is likely to occur without surgical ● Maintain patent airway; continued use of
intervention incubator if indicated
- Especially if it is tracheoesophageal since ● Suction as needed, change position
there is no intake of food frequently; avoid hyperextension of neck
○ Hyperextension of neck can stretch
✓ Urgency of surgery depends on the severity of the esophagus and trachea as well
condition na wala pa nagheal ang site
● Maintain IV fluids, antibiotics, and parenteral
Fig. 22 Gastrostomy nutrition as prescribed.
● Maintain adequate nutrition – gastrostomy
Fig. 24 Esophageal ○ NPO – to allow continuous healing
Anastomosis on the post- operative site
● Monitor strict intake and output. Determine
Esophageal anastomosis client’s nutrition
– creating a connection to ● Monitor daily weight.
make an opening from the ○ Reflection of client’s progress (weight
esophagus directly into the should increase)
● Inspect the surgical site for signs and ● TYPE III/ C
symptoms of infection. ○ upper end blind; lower end connects
● Monitor for anastomotic leaks as evidenced into trachea
by purulent drainage from the chest tube, ○ esophagus has a blind pouch
increased temperature, and increased white ○ trachea is connected directly to the
blood cell count. stomach
○ Anastomotic leaks – starts once ■ Air enters the stomach, which
infection sets in; formation of leads to bloating. Some of the
purulent discharges (pus gastric juices can go to the
trachea which could lead to
● Observe for signs of stricture at the aspiration
anastomosis site (e.g., poor/refusal to feed,
dysphagia, drooling, regurgitated undigested ● TYPE IV/D
food). ○ Both the trachea and esophagus has
an opening to the stomach
○ There is a risk for aspiration since
the esophagus has an opening in the
ESOPHAGEAL ATRESIA/TEF
trachea
■ Although food is able to go to
the stomach, food could still
● The esophagus terminates before it reaches enter the trachea which could
the stomach, ending in a blind pouch, and/or reach the lungs
a fistula is present that forms an unnatural
connection with the trachea. ● TYPE V/E
○ Fistula – abnormal connection ○ Esophagus is connected to the
between two body parts; mag stomach but still has an opening
reconnect siya sa lain body part connected to the trachea
○ Atresia – no opening connection; ■ could lead to bloating
wala nag connect sa organ (because of air from the
● Congenital anomaly trachea) and/or aspiration
(because of the food)
Types TEA/TEF
CLINICAL MANIFESTATION
● TYPE I/A
○ lower segments of the esophagus 1. Excessive amount of secretions constant
are blind drooling large secretion from the nose
○ air is directly connected to the lungs 2. Intermittent/unexplained cyanosis
○ closed esophagus – food isn’t a. Compromised oxygenation/aspiration
digested because it doesn’t reach the 3. Coughs and chokes
stomach so the patient vomits a. Aspiration
○ mubalik ra ang food sa taas since 4. Fluids returns through nose and mouth
wala man siyay padulngan = a. Saliva returns upward since there is
vomiting no opening in the esophagus
5. Regurgitation & vomiting
6. Abdominal distention
● TYPE II/ B a. If trachea is connected to the
○ upper end of esophagus opens into stomach
the trachea; blind lower segment b. Bloating
○ combination of fistula and atresia 7. Inability to pass a small catheter through the
○ esophagus has a connection to the mouth or nose into the stomach
trachea, but the esophagus also has a. Catheter returns upward since there
a blind pouch so it isn’t connected to is a blind pouch, wala nay maadtuan
the stomach ang catheter
■ Instead of the stomach, food
is diverted inside the trachea
which is connected to the DIAGNOSTIC EVALUATION
lungs, which could cause
aspiration ● Maternal history of polyhydramnios
● X-ray of abdomen and Chest X-ray
○ To determine the type of fistula
● X-ray with radiopaque catheter
○ Insertion of catheter with a dye. The increased temperature, and increased white
dye serves as a guide. blood cell count
○ Subayon sa dye 10. Observe for signs of stricture at the
● Insertion of a catheter
anastomosis site (e.g., poor/refusal to feed,
Management dysphagia, drooling, regurgitated undigested
food).
Includes maintenance of :
● a patent airway
● prevention of aspiration pneumonia ○ gastric Hypertrophic Pyloric Stenosis
or blind pouch decompression
● supportive therapy
● Congenital hypertrophy of the circular
● surgical repair
muscles of the pylorus in the stomach; the
muscle becomes progressively thickened
1. Drug Therapy
and elongated with narrowing of the pyloric
● Antibiotics – for respiratory infection
canal.
● The stenosis usually develops in the first few
2. Surgery
weeks of life, causing projectile vomiting,
● Primary repair – esophageal anastomosis
dehydration, metabolic alkalosis, and failure
● Gastrostomy - feeding
to thrive.
● Esophagostomy - drain secretions
Assessment
Pre-operative Interventions
● Absence of ganglion cells in a portion of the 1. Administer enema as ordered with Isotonic
large intestine solution only
● Is a parasympathetic nerve cells that 2. Do not treat loose stools – child is
regulates peristalsis in the intestine constipated
● The absence of the ganglion cells would 3. Administer TPN - Total Parenteral Nutrition
result to absence peristalsis and affected allows gastric rest, or allows the stomach to
colon becomes dilated and filled with feces relax
and gas 4. Instruct parents on colostomy care, correct
● The disease may be a familial congenital diet; feed pt. 24 hrs post-operation
defect or may be associated
Intussusception
Factors
Imperforate Anus
1. Hyperperistalsis and unusual mobility of ● Congenital malformation in which there is no
cecum and ileum anal opening or there is stricture of the anus
2. Lesion such as polyp and tumor ● Etiology is unknown
a. It is considered a surgical abdominal ● An arrest in embryonic development on 7th
emergency in children to 8th week of intrauterine life
b. Mechanical Bowel Obstruction ● A membrane remains and blocks the union
Occurs: intestinal walls press against between the rectum and the anus
each other causing inflammation, ● Blind rectal pouch with normal anus
edema and decreased blood flow.
c. May progress to necrosis, perforation Clinical Presentation
and peritonitis. ● No stool passage with in 24 hours after birth
d. Gangrene of the bowel ● Meconium stool from other orifice
● Only a dimple indicates the site of the anus
Clinical presentation ● Inability to insert thermometer
Diagnosis
1. Sudden onset of abdominal pain (in a ● Digital rectal exam
healthy baby) ● Ultrasound
2. Infant cries out sharply and draws knees up ● Abdominal X-rays
to abdomen Management
3. Vomiting occurs and increases overtime ● If suspected, do not take rectal temperature
(Bile stained vomitus) ● Pre-operative care
4. Currant jelly stool ○ Monitor for the presence of stool in
5. Signs of shock the urine and vagina (indicates a
6. (+) for Occult blood in stools fistula) and report immediately.
7. Sausage-shaped mass in RLQ ○ Administer IV fluids as prescribed
○ Prepare the child and parents for the
surgical procedures, including the
Diagnosis potential for colostomy
Often based on history and physical examination
alone ● Post-operative Care
○ Expose perineum to air
● Barium enema ○ Check bowel sounds
○ Is definitive (in 75% of cases) ● It is ○ NGT for gastric decompression
therapeutic and curative in most ○ Change position frequently
cases with less than 24-hour duration ○ Oral feeding started gradually as
soon as peristalsis function returned
● Digital rectal exam ○ Instruct the parents to use only a
○ reveals mucous, blood water-soluble lubricant and to insert
Immediate Treatment the dilator no more than 1 to 2 cm
● IV fluids
● NPO status
● Diagnostic barium enema
Displaced Urethral Openings
● Surgery – manual reduction of invagination
○ resection with anastomosis HYPOSPADIAS
○ possible colostomy (gangrenous) ● Males: urethra opens on the lower surface of
Nursing Management the penis
● Provide routine pre- and post-operative care ● Females: urethra opens into the vagina
for abdominal surgery
● Monitor fluid and electrolyte status EPISPADIAS
● Maintain nutrition and hydration ● Only in males
● Resume feedings 24 hours post operative
● Urethra opens on the dorsal surface of the ○ Handwashing and avoiding exposure
penis to infection.
● Congenital absence of the upper wall of the
urethra ● When feeding infants and young children,
● Procreation may be interfered with in severe use a small, straight-handled spoon to push
cases food to the side and back of the mouth.
● Increased risk of urinary tract infection ● Encourage fluids and foods rich in fiber.
Management ● Constipation results from decreased muscle
● Circumcision is delayed until surgical repair tone, which affects gastric motility.
● Surgical repair ● Provide good skin care because the skin is
○ Meatotomy - moving the meatus to dry and prone to infection.
the tip of the glans penis or the ● Family education – counseling
orifice to be in front of the vaginal developmental progress
opening
Assessment
● Fidgets with hands or feet or squirms in the
seat
● Easily distracted with external or internal HIGH RISK TODDLER
stimuli
● Difficulty with following through on
instructions
● Poor attention span BURNS
- an injury to body tissue caused by
excessive heat
- most severe form of trauma to the
integumentary system
TYPES OF BURNS
1. PARTIAL THICKNESS
PHASES/STAGES OF BURNS
1. EMERGENT PHASE
2. SHOCK PHASE
- fluid shift from plasma to interstitial causing
hypovolemia
ASSESSMENT FINDINGS
Minor Burns
• Antibiotic
- prophylaxis
- Predispose to develop infection because of skin
Breakdown
• Analgesic ointment
- to relieve pain - Taking healthy skin from one part of the
body and transplant (move) it to cover skin
• Gauze bandage that's damaged or missing
- prevent exposure to environment - Auto graft - self; skin used for grafting is
- Decrease incidence of infection from the patient itself
- Skin used is usually from the buttocks and
Moderate Burns abdomen
• do not rupture blisters - Tilapia skin is also used for skin grafting to
- prone to develop infections because of skin lessen or prevent scarring while promoting
breakdown wound healing
• analgesia/antipyretic ointment
• warm water and mild soap
• burn dressing – bulky dressing Additional Notes:
- magtubig if blisters break causing the fluids to ✓ Treatment depends on severity
leak. Gauze can quickly dampen if the dressing ✓ Severe burns if left untreated after 24 hours will
is thin lead
to death (because of fluid shifting, hypovolemic
shock)
✓ NOTE: Parameters such as vital sign (heart
rate),
urine output, adequacy of capillary filling, and
sensorium status determine adequacy of fluid
resuscitation
Fig. 9 Antibiotic Fig. 10 Bulky dressing
✓ Discourage the use of toothpaste. Toothpastes
Severe Burns only have a cooling effect.
- Can worsen the burn
a. Supportive Therapy; Fluid Management - Can make the burn more
● Can lessen the occurrence of hypovolemic
shock if done right away COMPARING OPEN AND CLOSED BURN
● Crystalloid solutions: Lactated Ringer THERAPY
- - Most common
● Colloid solutions: such FFP
- dextran is commonly used
- faster action
● Catheterization
- Monitoring and assessing the condition of
client for hypovolemic shock and
remobilization
b. Wound Care
● open or closed burn therapy, hydrotherapy
● Hydrotherapy – submerging patient in a
whirlpool/bath tub to prepare for
debridement (facilitates skin softening)
c. Drug Therapy
● Topical antibiotic (Silver Sulfadiazine)
● Systemic antibiotics – prevent infection
● Tetanus toxoid/HTIG - SOP OTHER CONSIDERATIONS IN THE
● Analgesic – morphine sulfate TREATMENT OF BURN
d. Physical Therapy
● to prevent disability caused by scarring,
contracture 1. Hand injuries
● Contracture - permanent tightening of the - each individual finger and toes should be dressed
muscles, tendons, skin, and nearby tissues and movement encouraged
that causes the joints to shorten and - to prevent contractures
become very stiff. - creates tissue scarring in-between the fingers or
e. Surgery toes resulting in webbed hands or feet
● Escharotomy 2. Facial burns
- Surgical removal of eschar - open technique with ointment use only
● Debridement open technique – eyes, mouth, and nose
- Removal of dead tissue are left open
● Skin grafting ointment – keeps area moist
3. Topical antimicrobials
- silver sulfadiazine and sulfamylon - used only
for major burns and should not be used in 2. Monitor alterations in fluid and electrolytes
outpatients 3. Promote maximum nutritional status
silver sulfadiazine – if patient is still 4. Prevent wound infection
admitted (needs skill, wrong application 5. Prevent GI complications
can cause irritation) sulfamylon – once patient is ● Curling’s ulcer – common burn
discharged complication
4. Any burn that does not heal in a month - Burn patients undergoes stress. Stress
should be referred to a burn surgeon promotes the GI tract to produce more acids.
If client has no intake, this will lead to
erosion of the mucosa, resulting in curling’s
ulcer
● Patients are usually given antacids
6. Provide health teachings
ETIOLOGY
Additional Notes:
✓ Athetoid and tremor are likely the same except
that Athetoid can still provide balance while tremor
has no balance at all.
✓ Cerebral Palsy entails Paralysis and Weakness.
TYPES OF PARALYSIS
COMMON PROBLEMS
Depends on affected area
Additional Notes:
✓ People with cerebral palsy inside rehabilitation
Facilities are called “Residents” because they live
in that area with a purpose.
✓ They are physically challenged or physically
handicapped because they are able; they only have
problems in certain areas.
MEDICAL MANAGEMENT
1. Drug therapy PT, speech therapy, audiotherapy, OT, etc.
Antianxiety – given when patient is anxious 2. Assess the child's
skeletal muscle relaxants – for stiff muscles developmental level and
local nerve block intelligence.
2. Speech/audiotherapy Mental retardation
3. Physical/occupational therapy 3. Encourage early intervention and participation
Physical - ADL, Paralympics in
Occupational – taught how to make a living school programs.
NOTE: Surgical interventions are reserved for the 4. Prepare for using mobilizing devices.
child Teach the client the different techniques in using
who does not respond to more conservative the mobilizing devices
measures 5. Encourage communication and interaction with
(PT) or for the child whose spasticity causes the
progressive child on his or her developmental level rather than
Deformity. chronological age level.
6. Provide a safe environment
7. Assist in ADL
8. Provide safe appropriate toys for the child's age
NORMAL DEVELOPMENT VS. CEREBRAL
and
PALSY
developmental level.
9. Position the child upright after meals.
10. Administer medications as prescribed to
decrease
spasticity.
11. Therapy
INGESTION OF POISONS
1. Salicylate poisoning
• aspirin, oils of wintergreen
• decrease RR
• Toxicity begins at doses of 150 - 200 mg/kg.
• S/S – CNS depression
- Vomiting (initial manifestation)
- respiratory failure
2. Acetaminophen poisoning
• commonly used analgesics
• risk for liver damage
• Antidote – mucomyst (N-Acetylcysteine)
• S/S – vomiting, liver tenderness, abdominal pain Fig. 18 Photo of Lead Poisoning
3. Lead Poisoning (Plumbism)
• common in toddlers and preschoolers Blood Lead Level Test
• Prevention: Lead-free •Used for screening and diagnosis
• Lead interferes with RBC function •Intervention depends on the level of lead in the
• Lead value of 15ug/dl – health hazard body
• Symptoms appear when lead level is – 70ug/dl
• Most serious effect: Lead encephalitis
• Air, soil, water, houses, ceramic cookware, solder
used in
metal cans and pipes
- Toys also contains lead
- The brighter the color, the higher the lead
content
• S/S:
Abdominal complaints – colicky pain,
Constipation, vomiting
Pallor – this concerns the RBC
Irritability
Loss of coordination
Encephalopathy
(+) lead in the blood
NURSING ACTION
OTHER SYMPTOMS
SYMPTOMS
Additional Notes:
✓ Cystic fibrosis affects the cells that produce
sweat,
mucus, and digestive enzymes Fig. 24 Areas affected by Cystic Fibrosis A
✓ Thick mucus may build up in the lungs and
block
the airways, which makes it ideal of bacterial
growth and may lead to lung infections
-
Bacteria thrives in thick, tenacious
secretions
✓ The fluid can also block tubes in the pancreas,
this
may hinder the digestive enzymes. This can cause
malnutrition and vitamin deficiency
✓ Sweat can also become very salty. Thus, a large
amount of salt is lost when sweating. This can upset
the mineral balance in the blood, which may result
growth and may lead to lung infections
-
Bacteria thrives in thick, tenacious
secretions
✓ The fluid can also block tubes in the pancreas,
this
may hinder the digestive enzymes. This can cause
malnutrition and vitamin deficiency
✓ Sweat can also become very salty. Thus, a large
amount of salt is lost when sweating. This can upset
the mineral balance in the blood, which may result
in serious health conditions, such as dehydration,
decrease BP, stroke, and rarely death.
✓ Although people with the disorder require daily
care,
they can still live a normal life.
✓ There is no cure for cystic fibrosis. People with
CF
will not live longer lives because complications will
appear over time.
✓ Most common among white people; less
common
Fig. 25 Areas affected by Cystic Fibrosis B in Asians
✓ Caused by a defect in the cystic fibrosis
transmembrane conductance regulator gene
(CFTR gene)
✓ In order to have cystic fibrosis, a child must
inherit
a faulty gene from each parent. Children who
inherit one normal and one faulty gene will be a
carrier of the defective gene and may not usually
develop CF. However, they may pass the defective
gene on their own children.
✓ A genetic test or blood test is used for newborn
screening
✓ Goals of treatment are to prevent and control
infections that occur in the lungs
-
Fig. 26 Example Inheritance Pattern To loosen the mucus in the lungs
of Cystic Fibrosis -
To treat and prevent intestinal blockages
-
To provide adequate nutrition
-
To prevent dehydration
Increase bacterial
invasion•
The most common symptoms are pancreatic
enzyme deficiency caused by duct blockage,
progressive chronic lung disease associated with
infection, and sweat gland dysfunction resulting in
increased sodium and chloride
sweat concentrations.
Fig. 27 Cystic Fibrosis
4 Symptoms Same With Celiac Disease
SYMPTOMS •Malnutrition
Additional Notes: •protuberant abdomen
✓ Cystic fibrosis affects the cells that produce •steatorrhea
sweat, •fat-soluble vitamin deficiency
mucus, and digestive enzymes
✓ Thick mucus may build up in the lungs and A. RESPIRATORY
block 1. Wheezing and dry nonproductive cough
the airways, which makes it ideal of bacterial 2. Dyspnea
3. Cyanosis Normal - if sweat chloride concentration is 20
Poor diffusion of oxygen meq/L or
4. Clubbing of the fingernails and toes lower than 40mEq/L.
Determine the length of oxygen deprivation •Chloride concentrations of 50 to 60 mEq/L are
5. Barrel chest highly
Result of compensatory mechanism of the suggestive of cystic fibrosis and require a repeat
respiratory area test.
6. Repeated episodes of bronchitis and pneumonia •A chloride concentration higher than 60 mEq/L is
Complications of CF that causes death a Positive result
B. GASTROINTESTINAL
1. Meconium ileus in the neonate
2. Intestinal obstruction
● Pain
● abdominal distention
● severe constipation
● nausea and vomiting
3. Steatorrhea (frothy, foul-smelling stools) easy
bruising and anemia
4. Malnutrition and failure to thrive
5. Generalized edema due to hypoalbuminemia
albumin is responsible to maintain oncotic pressure
para dili basta basta mag transfer ang fluids and
other electrolytes to other compartment. If wala na,
this would lead to shifting of bodily fluids, resulting
in generalized edema (ex. ascites) Fig. 28 Quantitative Sweat Chloride Test
6. Rectal prolapse
due to large, bulky stools and lack of the 2. Chest x-ray
supportive fat pads around the rectum •Film reveals atelectasis (lung collapse) and
obstructive
C. INTEGUMENTARY emphysema.
1. Abnormally high concentrations of sodium and 3. Pulmonary function tests
chloride in sweat •Provide evidence of abnormal small airway
2. Parents reporting that the infant tastes “salty” function.
when kissed 4. Stool, fat, enzyme analysis:
3. Dehydration and electrolyte imbalances, • A 72-hour stool sample is collected to check the
especially during hyperthermic conditions fat and/or enzyme (trypsin) content
Hyperthermic conditions = due to excessive •Food intake is recorded during the collection
sweating during -Can give an explanation about the fat content in
the client’s stool
D. REPRODUCTIVE 5. Duodenal analysis
1. Delay puberty in girls. •nasogastric tube is inserted to aspirate duodenal
2. Infertilityhighly viscous cervical secretions secretions
3. Sterility •to check if GI area is affected
caused by the blockage of the vas deferens by
abnormal secretions or by failure of normal THERAPEUTIC MANAGEMENT
development of duct structures. 1. RESPIRATORY SYSTEM
•Goals of treatment include preventing and
Additional Notes: treating pulmonary infection by improving aeration,
✓ Respi, GI, and Repro have increase mucus removing secretions, and administering
production if patient has CF antimicrobial medications.
a. Chest physiotherapy
DIAGNOSTIC TESTS - chest tapping
1. Quantitative Sweat Chloride Test b. Aerosol Therapy - nebulization
• the most reliable diagnostic test Bronchodilator
Pilocarpine – a cholinergic drug that stimulate Antimicrobial
production of sweat Mucolytic – loosen mucus
-the sweat is collected, and the sweat c. Use of a Flutter Mucus Clearance Device
electrolytes are measured -
- a device is placed on a child to collect the a small, hand-held plastic pipe with a stainless
sweat steel ball on the inside
•
- ✓ Malabsorption can lead to permanent intestinal
chest physiotherapy damage
- -
can loosen secretions In children, malabsorption can lead to
d. Use of a ThAIRapy vest device abnormal growth and development
- ✓ Some gene variation may increase the risk of
provides high-frequency chest wall oscillation to developing the disease
help loosen secretions ✓ Celiac disease may be triggered or become
active for the first time after surgery, emotional
2. GASTROINTESTINAL SYSTEM stress, viral infections, pregnancy, and childbirth
a. The goal of treatment for pancreatic insufficiency ✓ Factors that may predispose a person to celiac
is to replace pancreatic enzymes disease are Type 1 diabetes, Down syndrome,
b. The amount of pancreatic enzymes administered Autoimmune thyroid disease, and Rheumatoid
is adjusted to achieve normal growth and a arthritis
decrease in the number of stools to two or three ✓ Doctors recommend gluten-free mineral and
daily. vitamin supplements for chronic nutritional
c. Enteric-coated pancreatic enzymes should not be deficiency
crushed or chewed. ✓ Doctors recommend steroids for severe intestinal
d. Pancreatic enzymes should not be given if the damage to control inflammation
child isNPO. ✓ Inflammation in the small intestine starts to
e. Encourage a well-balanced, high-protein reduce
(hypoalbuminemia), high-calorie diet; multivitamins once gluten has been removed from diet
and vitamins A, D, E, and K are also administered. -
F. Assess weight and monitor for failure to thrive Regrowth and complete healing of the villi
(due to weight loss). may take several months to years
g. Monitor for constipation (increase mucus) and
intestinal obstruction.
h. Ensure adequate salt intake and fluids that
provide an adequate supply of electrolytes during
extremely hot weather and if the child has a fever.
Children with cystic fibrosis are easily dehydrated
because of increased perspiration
HOME CARE
CELIAC CRISIS
INTERVENTIONS
1. Maintain a gluten-free diet, substituting corn, rice,
and COMMON HEALTH PROBLEMS IN
millet as grain sources. PRESCHOOL AGE
Gluten can be found in preservatives, vitamin
supplements, herbal supplements, toothpaste and
mouthwash, hair and skin products, and lipstick BRONCHIAL
2. Instruct parents and child about lifelong
elimination of ● it is an obstructive disease of the lower
gluten sources such as wheat, rye, oats, and barley. respiratory tract
3. Administer mineral and vitamin supplements, ● often cause by an allergic reaction to an
including environmental allergen
iron, folic acid, and fat-soluble supplements A, D, E, ● allergic reaction results in histamine release
and ○ airway responses causes inflammation,
K constriction, obstruction
4. Teach the child and parents about a gluten-free
diet and Allergic reaction results to 3 main airway
about reading food labels carefully for hidden responses
sources of a. Edema of mucous membrane
gluten ● Presence of inflammation
5. Instruct the parents in measures to prevent celiac b. Spasm of the smooth muscles
crisis. ● Smooth muscles are tightened
Prevent exposure from any other infection because of the reaction of the
Small frequent feeding histamine release, creating a narrow
airway, which causes constriction ● Chronic - more than 6 months, long
and obstruction period of time
c. . Accumulation of secretions
● The release of histamine thickens the Severe attack
wall which releases secretions a. Shortness of breath
b. Use of accessory muscles
c. Retractions
d. Nasal flaring
e. Irritability (earliest sign hypoxia)
f. Diaphoresis
DIAGNOSIS
a. ABG – respiratory acidosis
b. Peak flow meter - An objective way to
Additional Notes: measure airway obstruction
● Compromised air exchange because of the ● The most reliable early sign of an asthma
secretions and the spasm. The air in the attack is a drop in the in the child peak
alveolus becomes trapped creating the expiratory flow rate
wheezing sound
MEDICAL MANAGEMENT
a. Drug therapy
RISK FACTOR ● Bronchodilators - Beta-2-agonist
bronchodilator, xanthine derivative
a. Family history of allergies and asthma
● Antiasthma - Corticosteroids, Mast cell
b. Client history of eczema
stabilizer , leukotriene inhibitors
- Contact dermatitis/eczema
● Antibiotics
inflammation of skin that cause ○ Prophylaxis treatment since there is
allergens increase production in mucus,
increasing the chance of bacterial
growth
CLINICAL MANIFESTATIONS
b. Hyposensitization – limit allergens
a. Expiratory wheeze c. Exercise – aimed to increased expiratory
● Narrow bronchial airways function
b. Cough d. Incentive Spirometer – alternative to
c. Thick tenacious secretions exercise
d. Barrel chest - if chronic ● Used daily
● Narrow bronchial airways ● Measures the amount and rate a person
● Acute - within 6 month breathes in order to diagnose illness or
period/temporary determine progress of treatment
● Pia (24 hr period)
* From the word “nephro” it affects the kidney
*Before its enlargement, manifestations are
asymptomatic.
NURSING INTERVENTIONS
1. Place client in high fowler’s position
● Facilitates lung expansion ASSESSMENT
2. Administer oxygen as ordered
● Low flow if there’s no doctor’s order since ● Palpable mass
the airways are constricted. If the airways ● Hematuria
are constricted, there is impaired diffusion ● Hypertension
of gasses so pwede mag pundo if dili ● Anemia
maapas ug pagawas ang gas ● Low grade fever
3. Administer medications as ordered
4. Provide good hydration
● Can facilitate proper expulsion of secretions
5. Provide chest physiotherapy
6. Promoting energy conservation
7. Monitor respiratory function
8. Provide family health teachings
● Include what triggers asthma attack
● Allergy-causing foods
Additional Notes:
* The kidneys are responsible for removing wastes
from the body, regulating electrolyte imbalance and
blood pressure, and stimulating red blood cell
production
* As there’s irritation with the renal parenchyma,
hematuria manifests
* Regulator of blood is affected, thus, hypertension
* Numbers 4 and 5 helps with loosening secretions follows
WILM’S TUMOR * Anemia happens as blood circulation has been
affected
● Nephroblastoma
● A large malignant tumor that develops in the
renal parenchyma DIAGNOSTIC TESTS
● Arises from bits of embryonic tissue that ● Sonogram
remains after birth ● CT Scan
● It accounts for 20% of solid tumors in childhood ● IVP - intravenous pyelogram
● Tumor is rarely discovered until it is large ○ Introduction of dye to determine the
enough to be palpated affected part or the area of the mass
Additional Notes
4. Provide routine preoperative care
STAGING OF NEPHROBLASTOMA
POSTOPERATIVE
STAGE 1 ● Limited to kidney 1. Assess the respiratory, circulatory, fluid and
● Not easily electrolyte status
diagnosed 2. Monitor patency and adequacy of urinary
status
STAGE 2 ● Tumor extends 3. Observe for any postoperative complications
beyond kidney but (signs of infection)
completely 4. Provide care for child receiving radiation and
encapsulated chemotherapy
Additional Notes:
* Its different types depend on the location
* Common manifestations are frequent urination,
painful urination and dysuria
* Not all manifestations are present to people with
UTI as it depends on the infected
ASSESSMENT FINDINGS
1. Low grade fever
2. Abdominal pain - lower region
3. Burning pain upon urination (dysuria)
4. Hematuria
5. Foul-smelling
6. Urinary frequency (polyuria)
NURSING INTERVENTION 7. Enuresis - common sign for preschooler
PREOPERATIVE a. Cannot withhold urine
1. Do not palpate the abdomen
2. Handle the child carefully DIAGNOSTIC TEST
a. Do not place in prone position to
avoid rupturing of the capsule ● Urine analysis - presence of pus cells and
3. Monitor BP, Intake, and Output bacteria
a. Include the VS as well ○ Clean catch
○ WBC count is increased
TYPES
TREATMENT
1. Acute: Occurs 2 to 3 weeks after a
● Antibiotic streptococcal infection
● Analgesic - for the pain 2. Chronic: Can occur after the acute phase or
● Antispasmodic - to relieve spasm slowly over time
● Increase fluid intake a. Manifestations usually extend
○ Facilitate passage of bacteria beyond 6 months
INTERVENTIONS
1. Monitor vital signs, weight, intake and output,
and the characteristics of urine (color and
CAUSES foam).
a. Fluid retention can cause an
1. Immunological diseases increase in weight
2. Autoimmune diseases b. I/O for fluid retention and Oliguria
3. Antecedent group A beta-hemolytic 2. Limit activity; provide safety measures.
streptococcal infection of the pharynx or skin 3. Provide high-quality nutrient foods
4. History of pharyngitis or tonsillitis 2 to 3 weeks a. Restrictions depend on the stage and
before symptoms severity of the disease, especially the
extent of the edema (LSLF).
b. In uncomplicated cases: Regular diet
is permitted but sodium is restricted
to a “no added salt to foods” diet.
(bland diet)
c. Moderate sodium restriction:
Hypertension or edema. Increase in
sodium attracts more water which
can increase BP
d. Foods high in potassium are
restricted during periods of oliguria.
e. Protein is restricted if the child has
severe azotemia resulting from
prolonged oliguria.
4. Monitor for complications
a. Azotemia
b. Dialysis (if chronic)
5. Administer diuretics, antihypertensive, and INTERVENTIONS
antibiotics as prescribed 1. Monitor vital signs, intake and output, and daily
6. Instruct the parents to report signs of bloody weights.
urine, headache (increase BP), or edema 2. Monitor urine for specific gravity and albumin.
(progression). 3. Monitor for edema.
7. Instruct the parents that the child needs to 4. Nutrition: A regular diet without added salt is
obtain appropriate adequate treatment for prescribed if the child is in remission; sodium is
infections, specifically infections. restricted during periods of massive edema.
5. Corticosteroid therapy is prescribed as soon as
NEPHROTIC SYNDROME the diagnosis has been determined; monitor
the child closely for signs of infection.
● Increase permeability to plasma
a. Patient becomes
(protein-albumin)
immunocompromised
● Is a kidney disorder characterized by massive
6. Immunosuppressant therapy - reduce the
proteinuria, hypoalbuminemia
relapse rate and induce long-term remission
(hypoproteinemia), and edema.
7. Diuretics may be prescribed to reduce edema.
● Autoimmune process
8. Plasma expanders such as salt-poor human
● The primary objective of therapeutic
albumin may be prescribed for the severely
management is to reduce the excretion of
edematous child.
urinary protein and maintain protein-free urine
9. Instruct the parents regarding the signs of
● Patho: plasma enters the renal tubules –
infection and the need to avoid contact with
excreted in the urine = proteinuria Protein shift
other children who may be infectious.
causes altered oncotic pressure (swelling)
CLASSIFIED
1. Acute (rapidly developing) TONSILLITIS AND ADENOIDITIS
2. Chronic (slowly developing)
Tonsillitis refers to inflammation and infection of the
tonsils.
TYPES
Adenoiditis refers to inflammation and infection of the
1. Acute Lymphocytic Leukemia adenoids.
a. Primarily strikes children and young
adults Assessment
b. 80 - 85 % of childhood leukemia
c. The malignant cells involved is the ● Persistent or recurrent sore throat
lymphoblast ● Enlarged, bright red tonsils that may be covered
2. Acute Myeloid Leukemia with white exudate
a. Also known as - acute ● Difficulty in swallowing
nonlymphocytic leukemia ● Mouth breathing and an unpleasant mouth odor
● Fever
b. Cells involved as the granulocytes
● Cough
● Enlarged adenoids may cause nasal quality of
ASSESSMENT FINDINGS speech, mouth breathing, hearing difficulty,
snoring, and/or obstructive sleep apnea.
1. Anemia (weakness, pallor, dyspnea)
2. Bleeding (petechiae, bruise) Preoperative interventions
3. Infection (fever, chills, malaise)
4. Enlarged lymph nodes ● Assess for signs of active infection.
5. Enlarged spleen and liver (splenomegaly and ● Assess bleeding and clotting studies because
hepatomegaly) the throat is vascular.
6. Abdominal pain ● Prepare the child for a sore throat
postoperatively and inform the child that he or
7. Bone and joint pain she will need to drink liquids.
● Assess for any loose teeth to decrease the risk
of aspiration during surgery.
DIAGNOSIS
Goal of care: complete cure Interventions postoperatively
● Position the child prone or side-lying to facilitate 4. red eyes
drainage.
● Have suction equipment available, but do not 5. swollen lymph nodes
suction unless there is an airway obstruction.
● Monitor for signs of hemorrhage (frequent Interventions
swallowing may indicate hemorrhage); if
hemorrhage occurs, turn the child to the side and ● Monitor temperature frequently.
notify the physician. ● Assess heart sounds, rate, and rhythm.
● Discourage coughing or clearing the throat. ● Assess extremities for edema, redness, and
● Provide clear, cool, noncitrus and noncarbonated desquamation.
fluids. ● Examine eyes for conjunctivitis.
● Avoid milk products initially because they will ● Monitor mucous membranes for inflammation.
coat the throat. ● Monitor strict intake and output.
● Avoid red liquids, which simulate the appearance
of blood if the child vomits. MEDICATION
● Do not give the child any straws, forks, or sharp
objects that can be put into the mouth. ★ IVIG
● Administer acetaminophen (Tylenol) for sore ★ Aspirin
throat as prescribed. ★ steroids
● Instruct the parents to notify the physician if
bleeding, persistent earache, or fever occurs.
PARENT EDUCATION
● Instruct the parents to keep the child away from
crowds until healing has occurred.
● Follow-up care is essential to recovery.
● The signs and symptoms of Kawasaki disease
include the following:
KAWASAKI DISEASE
Ø Irritability may last up for up to 2
● Kawasaki disease is known as mucocutaneous months after the onset of symptoms.
lymph node syndrome and is an acute systemic
inflammatory illness. Ø Peeling of the hands and feet may
● The cause is unknown but may be associated occur.
with an infection from an organism or toxin.
● Cardiac involvement is the most serious Ø Pain in the joints may persist for
complication; aneurysms can develop. several weeks.
Assessment Ø Stiffness in the morning, after naps,
and in cold temperatures may occur.
Acute stage
● Record the temperature until child has been
● Fever afebrile for several days.
● Conjunctival hyperemia ● Notify the physician if the temperature is 101° F
● Red throat or higher.
● Swollen hands, rash, and enlargement of the ● Salicylates such as acetylsalicylic acid (aspirin)
cervical lymph nodes may be given.
● Signs of aspirin toxicity include tinnitus,
Subacute stage headache, vertigo, bruising; do not administer
aspirin or aspirin-containing products if child has
● Cracking lips and fissures been exposed to chickenpox or the flu.
● Desquamation of the skin on the tips of the ● S/sx of bleeding: epistaxis, hemoptysis,
fingers and toes hematemesis, hematuria, melena, and bruises
● Joint pain on body.
● Cardiac manifestations ● S/sx of cardiac complications chest pain or
● Thrombocytosis tightness (older children), cool and pale
extremities, abdominal pain, nausea and
Convalescent stage: Child appears normal but signs of vomiting, irritability, restlessness, and
inflammation may be present. uncontrollable crying.
● Child should avoid contact sports, if age
appropriate, if taking aspirin or anticoagulants.
DIAGNOSIS ● Avoid administration of MMR or varicella vaccine
to the child for 11 months post–intravenous
● fever x 3/5days immune globulin therapy, if appropriate.
● + 4/5 diagnostic criteria
1. erythema
2. rash on trunk
NURSING INTERVENTION
● Mites are small eight-legged parasites, they
are tiny (not visible with the naked eye), and
1. Institute skin isolation precautions burrow into the skin to produce intense
★ Head covering itching, which tends to be worse at night
★ Gloves ● Scabies attack at night
2. Use specific shampoo/comb
3. Provide health teachings on treatment and prevention
● Scabies may involve:
★ Check on other family members ➔ webs between the fingers,
★ Washing of bed linens ➔ wrists
★ No sharing of combs and hats ➔ Elbows
➔ knees,
➔ waist
IMPETIGO ➔ umbilicus,
➔ axillary folds,
➔ around the nipples,
● Superficial bacterial infection of the outer ➔ sides and backs of the feet,
layers of the skin ➔ genital area, and the buttocks.
● Etiology: Staphylococcus aureus/ Beta H.
streptococcus MANAGEMENT
● Incubation period – 2 to 5 days
● Period of communicability – outbreak of ● Medication (SCABICIDES) - Permethrin
lesion until it’s healed cream / Lindane lotion
● Mode of transmission direct contact ● Scabicides – meds to treat scabies
● Very contagious ● Lindane should not be used in children
younger than 2 years because of the risk of
ASSESSMENT FINDINGS neurotoxicity and seizures.
● Because it’s easily absorbed in the skin
● Well demarcated lesions
● Macules, vesicles (fluid), papule (pus) that Instruction:
rupture = moist erosio
● Once most area dries, scab is honey colored body is scrubbed with soap and water before
crus application
● Pruritus
leave on the skin for 8 – 14 hours
MANAGEMENT
then completely washed with warm water
● Topical antibiotic – bactroban
● Systemic antibiotic - penicillin or ● Stress importance of proper hygiene
erythromycin
INTERVENTIONS
NURSING MANAGEMENT
● When permethrin is used, the cream is
1. Implement skin isolation techniques massaged thoroughly and gently into all skin
surfaces from the head to the soles of the
Including child’s things
feet; care should be taken to avoid contact antistreptolysin O (ASO) titer
with the eyes.
● Household members and contacts of the ECG - Prolonged PR interval
infected child need to be treated at the same
time. leukocytosis
Evidence of previous
RHEUMATIC FEVER (RF)
group A streptococcal infection
● An inflammatory disorder that may involve + Throat culture or rapid streptococcal antigen test
the connective tissue of heart, joints, lungs
and brain
● Is an autoimmune disease that occurs as a two of the major criteria, or one major criterion plus
reaction to a group A two minor criteria, are present along with evidence
beta-hemolyticstreptococcal infection of streptococcal infection.
● It is precipitated by streptococcal infection
which is undiagnosed and untreated
● Antigenic markers for streptococcal toxin Exceptions are chorea and indolent carditis each
closely resemble markers of the heart of which by itself can indicate rheumatic fever.
valves; this resemblance causes antibodies
made against the streptococcal to also
attacks the heart valve MEDICAL MANAGEMENT
A CNS disorder characterized by abrupt, 2. Bed rest – is essential during the active process
purposeless involuntary movement of rheumatic fever to reduce cardiac workload
● any joints might be affected 1. Assess joints for pain, swelling, tenderness,
● begins with high fever associated with or limitation of motion
macular rash on chest, thigh 2. Promote maintenance of joint mobility
● Other symptoms included are: Anemia (passive ROM exercise)
● Anorexia weight loss 3. Change position frequently
4. Promote comfort and relief of pain
Other Polydipsia Polydipsia
5. Ensure bed rest
symptoms Polyuria Polyuria
6. Provide heat treatments
Polyphagia Polyphagia
7. Provide cold treatments as ordered – acute
Fatigue Fatigue
8. Provide psychologic support and encourage
Blurred vision Blurred vision
to verbalize feelings
Glyocosuria Glyocosuria
pruritus pruritu
DIAGNOSIS
Assessment TYPE 1 TYPE 2
● Fasting blood sugar – 126 mg/dl or greater
Age of onset 5 – 7 yr / Increasingly ● Random blood sugar – 200 mg/dl or greater
puberty ● With CBG and HGT
● 2 hours oral glucose tolerance test (OGTT) –
Type of Onset abrupt gradual
200 mg/dl or greater
Weight Marked weight Assessment ● Done together with FBS. Baseline data is
changes loss with obesity FBS result. Right after FBS, patient drinks
glucose (8oz) then blood is checked 2 hrs
after drinking.
● Glycosylated hemoglobin – provide
information about what the child’s glucose 5. Monitor Intake and Output every shift, weigh
level have been during the preceding 3 to 4 daily
months 6. Provide emotional support
7. Observe for complications
MANAGEMENT FOR TYPE I DIABETES DKA if type I = CNS complications = check level of
consciousness
Goal: to keep your blood sugars as close to normal
as possible to prevent the complications of diabetes
1. Insulin Therapy
2. Meal planning
3. Exercise
4. Stress management
5. Blood glucose and urine ketone
monitoring
NURSING INTERVENTION
SCOLIOSIS
FORMS
1. Structural / Progressive form
-“S” curve of the spine
-usually idiopathic
-does not disappear with position changes
-needs more aggressive treatment
MANAGEMENT
BONE TUMORS
A. OSTEOGENIC SARCOMA
NURSING MANAGEMENT
a. Provide routine preoperative care
● NPO, IVF, VS
Additional Notes:
✓ Malignancy – rapid growth in a bone tissue
● Client and family should undergo counseling
before and after amputation
b. Offer support or encouragement and accept
client’s response of anger and grief
ASSESSMENT c. Discuss to patient and family
● rehabilitation program (pre-op) and use of
a. Pain prosthesis
b. Swelling, redness ● crutch walking
c. Tender mass, warm to touch ● phantom limb sensation as normal
d. Limitation of movement recurrence
○ Associated with the swelling and pain ○ When you “feel” the amputated body
e. Pathologic fracture part.
○ a break in a bone that is caused by ○ It is often painful normal occurrence
an underlying disease especially after amputation
○ common struggle after amputation NURSING INTERVENTION
d. Prevent hip and knee contractures prone position
several times a day (unless otherwise ordered) ● Caution adolescent to continue to be careful
e. Provide stump care and avoid activities that may cause added
● Prone to infection stress to affected limb such as football and
weight lifting
○ Can cause pathologic fractures since
bones become fragile
Additional Notes:
✓ TERRAMYCIN – prophylaxis ointment to prevent
ophthalmia neonatorum caused by STI
B. CHLAMYDIA
CLINICAL FINDINGS
● Chlamydia trachomatis
a. Pain and swelling on affected part
● Most common STI
b. Palpable mass (tumor)
● May causes ophthalmia neonatorum, sterility in
c. Tender and warm to touch (swelling)
female or male, tubal pregnancy (ectopic
d. 15- 35% of clients have metastasis (invade other
pregnancy)
parts of body) at time of diagnosis
● Ewing’s sarcoma has poor
Signs & symptoms
prognosis compared to
● watery, gray-white vaginal discharge
osteosarcoma.
● vulvar itching
MANAGEMENT Treatment
● doxycycline
1. High doses of radiation therapy ● tetracycline
● Treatment should be aggressive ● azithromycin (most common)
because of the poor prognosis
2. Chemotherapy
3. Surgery C. SYPHILIS
● Crosses placenta after 16 week of pregnancy
DIAGNOSIS (dangerousfor oogenesis)
Additional Notes:
✓ SYPHILIS is dangerous when pregnant especially at
16 weeks due to Oogenesis (formation of organs)
because the bacteria can cross to the placenta that
can affect the growth of the baby
F. GENITAL WARTS
D. TRICHOMONIASIS
Treatment
● Metronidazole ANOREXIA NERVOSA
● douche with weak vinegar solution to reduce
pruritus ● A disorder characterized by refusal to maintain
a minimally normal body weight because of
a disturbance in perception of the size or
appearance of the body
● An eating disorder characterized by extremely
low bodyweight, body image distortion and an
obsessive fear of gaining weight.
● Eating disorder associated with mental
disturbance
○ Needs psychiatric evaluation if
○ client is suspected with anorexia nervosa
NURSING INTERVENTION
1. Monitor vital signs
2. Monitor intake and output
i. Fluid and electrolyte imbalance
3. Record food intake
4. Monitor weight
5. Encourage client to express feelings
6. Help client to set realistic goal for self
MANAGEMENT
7. Help client identify interest and positive aspect
1. Nutritional therapy of self
a. Total parenteral nutrition - Intravenous
b. Enteral tube feeding - NGF = OF
2. Behavior modification - Psychiatrist) Additional Notes:
3. Medication – antidepressant ✓ Difference between the two eating disorders is their
4. Counseling perception
Anorexia nervosa – payat pero feeling niya
a. Individual therapy taba
b. Group therapy -Prefers not to eat
c. Family therapy Bulimia – either no perception but has ideal
body shape/weight
-Cannot control food intake
BULIMIA NERVOSA
OBE
● Bulimia – refers to recurrent and episodes binge OBESITY
eating and purging
● accompanied by an awareness that eating ● An excessive accumulation of fat that
pattern is abnormal but not being able to stop increases body weight by 20% or more (IBW)
● Bulimic person is of normal of weight or slightly ○ Obesity is now among the most widespread
overweight or underweight medical problems affecting children and
● may abuse purgative, laxatives and diuretic to adolescents living in the United States and
aid in weight control other developed countries.
○ Obesity increases the child's risk of of
serious health problems such as heart
CLINICAL MANIFESTATION AND DIAGNOSIS
disease, DM type 2 and stroke
● Dental caries and erosion ○ It can also create emotional and social
● Throat irritation problems
● Electrolytes imbalance – hypokalemia ○ Often feels isolated from the peer group
○ Associated with the use of laxatives (insecurities)
○ And Diuretics ○ Embarrassed to participate in sports
● Behavior problem ○ Adolescents may have difficulty
○ drug abuse achieving a sense of identity if they are
○ alcoholism always excluded from group and if they
○ stealing don’t like their image in the mirror
○ BMI – most accurate method of ● mature due to peer pressure - a form of
assessment rebellion
■ Indicates relationship between height ● Children at greatest risk
and weight 1. have family in which alcohol or drug
abuse is present
Causes 2. suffer from abuse, neglect (feels
● Many different factors contribute to this euphoria)
imbalance 3. have behavior problems –
● between calorie intake and consumption aggressiveness and excessively
● Genetic factors- Obesity tends to run in rebellious
families 4. slow learners
● Dietary habits 5. have problems with depression and
○ fast food, processed snack foods, low-self esteem
○ and sugary drinks
○ use food as means of satisfying emotional
STAGES OF SUBSTANCE ABUSE
needs
○ indulging in late – night eating
● Physical inactivity- The popularity of television, Stage 0: Pre abuse or Curiosity stage
● computers, and video games results into an ● Describes the adolescent with an increased
increasingly sedentary lifestyle potential for substance abuse
● Need for peer acceptance; anger and
boredom
1. Suicidal talk
2. Preoccupation with death and dying
3. Signs of depression
4. Behavioral changes
5. Giving away special possessions and making
arrangements to take care of unfinished business
6. Difficulty with appetite and sleep
NUrsing intervention
1. Maintain a patent airway and adequate
If left untreated - you would loss him
ventilation
- *the lower the GCS, the more the
Citicoline
patient has arrested breathing; very
low GCS = intubate
2. Contussion - results from more severe
2. Monitor VS and NVS
blow that bruises the brain and disrupts
3. Observe for CSF leakage
neural function
4. Prevent complications of immobility
5. Prepare a client for surgery if indicated
S/S: Neurologic deficits depend on site and extent
6. Provide psychological support to client and
of damage LOC, sensory deficits, hemiplegia
family
(paralyzed half of body)
7. Client teachings: rehabilitation
3. Hemorrhage
Diagnostic Test
a. Epidural - blood between dura mater and skull
1. Skull x ray
laceration of middle meningeal artery during skull
2. CT scan
fracture blood accumulates rapidly
4. Fractures
Types of fractures 3. Cranioplasty - repair of cranial defect with a
- Linear metal or plastic plate
- Depressed
- Comminutes PREOPERATIVE NURSING INTERVENTION
- Compound (combination of both)
S/s: leakage of CSF from nose or ear 1. Routine pre op care
CSF - very clear and watery ang consistency 2. Provide emotional support
3. Shampoo the scalp and check for signs of
infection
4. Shave hair
5. Evaluate and record baseline vital signs and ● ● Penetrating wounds
neuro checks ● ● Spinal shock – occurs immediately
6. Avoid enema - ○ Insult to the CNS
7. Give pre op steroid as ordered - to ○ Several days to 3 months
decrease brain swelling ○ Absence of reflexes below the level
of the lesion
POST OPERATIVE NURSING INTERVENTION Management
1. Maintain a patent airway - - immobilization and maintenance of normal
2. Check VS and NVS spinal alignment to promote fracture healing
3. Monitor fluid and electrolytes - because we
are drawing fluids 1. Horizontal turning frames - Stryker frame
4. Assess dressing frequently and report for 2. Skeletal traction
any abnormalities a. Cervical tongs
5. Administer medications as ordered b. Halo traction
6. Apply ice to swollen eyelids, lubricate lids 3. Surgery
with petroleum jelly a. Decompression b.
7. Refer for rehabilitation b. Laminectomy
c. Spinal fusion
2. Level of injury
a. Cervical
- C1-CB (quadriplegia)
- Paralysis of all four
extremities
- Respiratory paralysis- C6
3. Mechanisms of injury
● Hyperflexion
● Hyperextension
● Axial loading – diving accidents