exam 2 Flashcards

(45 cards)

1
Q

Specific diets for different conditions: GI

A

Appendicitis: NPO for surgery
Celiac Disease: Foods Allowed:
Potato, soy, rice or bean flour
Cornmeal, flax, quinoa
Plain, fresh, or frozen fruits and vegetables
Meat, fish, beans, peanut butter, nuts
Milk and milk products (unless made with gluten additives)
Butter, margarine, salad dressings, sugar, honey, jelly, marshmallows ground coffee, tea
Foods to Avoid
Wheat products: rye, barley, oats, durum flower, farina
Creamed or breaded vegetables, canned backed beans, some French fries
Malted milk, flavored or frozen yogurt
Meats or poultry prepared with gluten or fillers, some egg substitues
Commercial salad dressings, prepared soups, condiments, sauces, nondairy cream substitutes, licorice
Biliary Atresia: Give A, D, E, K
GERD: smaller more frequent feedings

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

childhood obesity risk factors and treatments

A

..

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

appropriate nursing interventions for GERD

A

Smaller, more frequent feedings
Keeping child upright for 30 min after feeds
Administer proton-pump inhibitors
Educate parents on both pharm and non-pharm interventions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

care of the patient with appendicitis

A

Observe for pain be suddenly relieved without intervention
Monitor temperature
Keep NPO for surgery
Administer IV pain meds
Post-op care may include IV antibiotics (if perforated)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

classic s/s of various GI disorders

A
Appendicitis:
Abdominal pain- RLQ 
N/V
Fever
small frequent soft stools
when pain goes away- they have perforated
Meckel's Diverticulum: 
Bleeding
Anemia
Abdominal pain (when obstruction occurs)
Abdominal distention
Hypoactive bowel sounds
Biliary Atresia: 
Jaundice 
Clay colored stool
Failure to thrive 
Enlarged liver/spleen
Elevated bilirubin, aks phos, liver enzymes
Pyloric Stenosis
Projectile vomit- fresh milk 
Weight loss
Progressive dehydration
Lethargy 
Celiac Disease	
Diarrhea
Steatorrhea (fatty stools)
Constipation
FTT
Abdominal distension or bloating
Irritability
Dental disorders
Anemia
Delayed onset of puberty
Intussusception	
Sudden onset of intermittent abdominal pain
Knees drawn up
Vomiting and diarrhea
Currant-jelly stools
Lethargy
Sausage-shaped mass in upper abdomen
Gastroesophageal Reflux (GER)	
Vomiting or regurgitation
FTT
Irritability
Respiratory symptoms
Dysphagia or refusing to eat
Abnormal neck posturing
Abdominal pain
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Caring for child with Meckel’s Diverticulum

A
Diagnostic Tests
Abdominal x-rays
Meckel scan
Stool tests (for color, consistency, and blood)
CBC

IVF for NPO status
PRBCs if anemia is present
Prepare child and family for surgery if indicated
Pain control

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Cleft palate/cleft lip pre-op and post op

A
Protect the suture line!!!
Use elbow restraints
Position child in supine or side-lying
Avoid spoons, straws, pacifiers, or PO syringes
May breastfeed, may need special nipple for bottle feeding
Pain medication and keeping child calm
Lip: Lay on Back
Palate: Lay on Stomach
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Increased ICP manifestations/treatment

A

Intervene quickly to prevent long-term damage or death!
Symptoms
Headaches
Morning emesis with immediate relief
Complaining of blurry or double vision
Progress to seizure activity
herniated brain is the worst case from intracranial pressure

infant: 
Head enlargement
Anterior fontanel—tense, bulging, non-pulsatile
Scalp veins dilated
Cranial sutures separated
“Bossing” of frontal bone
“Setting-sun” eyes
Changes in LOC/irritable/lethargic
Opisthotonos
Poor feeding
Shrill, high pitched cry
Developmental delay
Seizures
Periodic/Irregular breathing is an ominous sign, precedes apnea
Older Child:
Headache, Nausea/Vomiting
Ataxia
Strabismus/Diplopia
Pupil response to light—sluggish or unequal
Papilledema
Changes in LOC
Potential Intellectual Impairment
Seizures
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Manifestations/treatment/teaching: seizures, spina bifida, cerebral palsy, meningitis

A

seizures
Types
Focal/Partial- 60% of seizures, impairment of consciousness, localization, and progression of the seizure, one hemisphere of the brain
General- absence and tonic/clonic seizures, affects the whole brain
Unknown- epileptic spasms where it is unclear whether the mod of onset is general or focal
Primary treatment- anticonvulsants
Secondary treatment- surgery, Nurse will do preop/postop care and discharge teaching
Education- help families cope, explain the importance of medication adherence, oral care (Dilantin)
Observe and report seizure activity
Time, oxygenation status, safety, take in everything, do not restrain, ease to the ground if standing
Danger- seizure lasting 30 minutes or so many seizures that the child cannot recover
Febrile seizures:
Treatment- identify cause of high temperature and treat

Spina Bifida
Defect without protrusion of the spinal cord or meninges.
These children don’t typically need immediate medical intervention
Benign and asymptomatic
Will note a dimple, patch of hair, or discoloration of skin
Education of presence and monitoring of symptoms of tethered cord

Cerebral Palsy
Mobility- critical to development in the child with CP. Treatment could include physiotherapy, pharmacological management, or surgery. PT/OT are very involved and include the parents on the process.
Nutrition- May have difficulty eating and swallowing r/t poor mouth, tongue, and throat control. They need more time and support. Special diets such as soft or pureed. Manual support of the jaw and proper positioning to help with chewing and swallowing and to prevent choking and aspiration. All efforts will be exhausted, barring the child isn’t suffering, before going to a feeding tube.
Support and Education- Lifelong disorder that based on severity could include daily intensive therapy from caregivers, encourage respite care, understand that when a child is admitted that it is a chance for the family to take a break. Try to not judge when they are gone. Education requires help from social work, parents, teachers, and support staff.

Meningitis
Can lead to brain damage, nerve damage, deafness, stroke, death
Must act fast!
Deterioration over 24 hours
Diagnosis with an LP and administer antibiotics after sample has been collected
Examination
Opsithotonic position (infant) or c/o neck pain
Positive Kernig and Brudzinski
Rash- petechial, vesicular, or macular
Interventions- aimed at reducing ICP and maintain perfusion, treating volume deficits, controlling seizures, and prevent injury from altered LOC
Isolation- Droplet isolation for first 24 hours after initiation of antibiotics, then standard precautions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Otitis media: cause, treatment, education

A

Inflammation of the middle ear with presence of fluid
Follows upper respiratory infection- strep and influenza infections most common
Complications- hearing loss, expressive speech delay, perforation, meningitis (EXTREME!)
Antibiotics vs observing, analgesics

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Trisomy 21: characteristics, G&D, education

A

The structures of the face are very distinct. You also will note that the nasal passages are smaller. In infants the depressed bridge of the nose leaves them a small nasal passage. With the protruding tongue and mouth open most of the time, keeping secretions clear is important. Dry mucous membranes will make eating and babbling/talking a challenge.
single palmer crease, short 5th finger that curves here separated 1st & 2nd toes
widel

Promotion of nutrition
Diffuclty with suck and feeding due to lack of muscle tone, small mouth, large tongue, underdeveloped nasal bone, and chronically stuff nose
Bulb syringe, humidification, and changing position will help with feeding, breast feeding is usually possible and the antibodies help with fighting infection
No need for special diets unless they have an underlying GI disease like celiac

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What dietary restrictions or additions are there for the following disorders? Galactosemia, PKU, Diabetes, Salt wasting CAH.

A

Galactosemia: No milk products, no breast milk, soy based formula

PKU: Special formula
Breast feed if mom is following PKU diet

DM1: carb control

DM2: Less trans-fats, more fruit/veggies, balanced, incorporate fav foods, portion size, exercise
Limit bad sugars

Salt wasting CAH: salt

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What does the nurse need to emphasize with medication teaching for the following endocrine disorders? Congenital hypothyroidism, Diabetes, CAH, Growth hormone deficiency, precocious puberty

A

Congenital Hypothyroidism: Education: s/s hyper/hypo, lifelong supplements, medications, not changing meds

DM1:
Teaching skills (glucose checks & admin. Insulin & nutrition
Administer insulin based on 1. Glucose levels, 2. For meals
Have parent check sugars in night after sports

DM2: Education on lifestyle modifications

CAH: Ambiguous genitalia: provide comfort to parents, encourage parent bonding, explain in simple terms
Non-salt: receives life-long supplements
Medications for Salt-Wasters
Need aldosterone replaced also
Florinef Acetate oral once a day
Also need an injectable form of cortisone ie Solu-cortef on hand to administer if child is vomiting and cannot keep medication down or when experiencing severe stress
Increased dietary salt encouraged
Medic Alert Bracelet

GH Deficiency: GH injections: sites, give at night (body naturally secretes at night)
Educate how to give it, very expensive

Precocious puberty: Dress according to dev stage, peers of same age
LHRH analogs or synthetic hormones that block the body’s production of the sex hormones.
Given IM once every 4 weeks. Usually see no side effects.
Girls: decrease in breast size or at least no more development
Boys: the penis and testicles may shrink back to normal size.
Height will also slow down to the expected rate before puberty
Discontinue when puberty is expected

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

How would the nurse’s approach to teaching a newly diagnosed diabetic four year old differ from a ten year old and a 17 year old?

A

Toddler: cake icing (not the best option) carb followed by protein or carb & protein (protein sandwich, nuggets, chocolate milk)
Fear of needles, strangers, picky eaters
Teen: scars, not fitting in, appearance

School age: rewards, games, sports
Teen: thinking of appearance, they think they are invincible- starting experimenting with drugs & alcohol, consider their mindset

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What advice would you give to a Type 1 Diabetic who wanted to join a soccer team?
What advice would you give to a Type 2 Diabetic who wanted to join a soccer team?

A

DM1: Have parent check sugars in night after sports (bottom out), Cells utilize blood glucose more effectively
Exercise lowers blood sugar
Helps insulin to enter the cell more readily
Insulin requirement is reduced
Always carry a carbohydrate source to treat hypoglycemia or take before exercise to prevent

DM2: hell yeah

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What careful considerations does the nurse need to make when talking with parents of a child diagnosed with precocious puberty?

A

Provide support and anticipatory guidance
Dress and activities should be appropriate for chronological age
Sexual interest usually match’s child’s age
After puberty, child is no longer different from peers
Child is fertile if untreated. No form of contraception is recommended unless the child is sexually active
Teach parents and child injection procedure if needed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

How would you teach the mother of a newly diagnosed baby with congenital hypothyroidism about how to recognize s/s of hyperthyroidism and hypothyroidism?

A
HYPO
prior to 6 weeks:
Poor feeding
Lethargy
Prolonged neonatal jaundice
Respiratory difficulty & bradycardia
Constipation
Hoarse cry
Large fontanels
after 6 weeks: 
Depressed nasal bridge
Short forehead
Puffy eyelids
Large tongue
Course dry lusterless hair
Large fontanels and wide cranial sutures
Umbilical Hernia
Abdominal distension
Hypothermia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What would you suggest to a mother who wants to breast feed her newborn recently diagnosed with PKU? What about a mother with a baby who has galactosemia?

A

PKU:
Special formula
Breast feed if mom is following PKU diet- NO phenylanine herself

Galactosemia:
No milk products, no breast milk, soy based formula

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Why is it important for parents to get to know their pharmacist?

A

Hidden galactose in meds

So pharmacists are away of their galactosemia

20
Q

How would you know if growth hormone therapy was effective? How would the nurse know when it may be time to stop the therapy?

A

Growth 4-4.8 inches the first year and 2.7-3.5 following year
Usually a prompt increase in growth rate after treatment starts (usually noticeable within three or four months.) then the rate slowly declines over time but continues to be greater than would be without treatment.

The decision as to when to stop meds is made jointly by parents, child, and doctor. Consider stopping treatment when growth slows to less than 1-2 inches per year. But usually epiphysis closure is definitive criteria to stop. Average length of treatment 6.5 years. Minimal side effects of medication. Arthralgia, myalgia, injection site reaction, edema. May see worsening of scoliosis and slipped cap epiphysis.

21
Q

How would you manage a sick day for a patient with DM I?

How would you manage a sick day for a patient with CAH who receives hydrocortisone pills each morning?

A

DM1:
Monitor blood glucose every 2-4 hours
Do NOT stop taking insulin
Monitor urine for ketones (Strip) every 2-4 hours
Maintain hydration
If able to tolerate food take soft bland foods and 8 oz of fluid per hour
Notify health care practitioner if vomiting and BS above 240

CAH: Lifelong replacement is needed with increased doses during periods of stress, surgery, infection, or injury.
salt wasters: Also need an injectable form of cortisone ie Solu-cortef on hand to administer if child is vomiting and cannot keep medication down or when experiencing severe stress

22
Q

HUS triad

A
  1. Hemolytic anemia
  2. Thrombocytopenia
  3. acute renal failure

Watery diarrhea- hemorrhagic colitis- triad of hus

23
Q

Pre-op care of Epispadias/Bladder Extrophy

A

Meticulous hygiene
Sterile, nonadherent moist dressing placed over exposed bladder
Moist barrier ointment for surrounding skin
Fluid management
Following primary surgery, nursing care is aimed at: decreasing pain and agitation, No crying, preserving pelvic immobility, maintaining ureteric catheter patency, maintaining operative site intact.
Parent teaching: Appearance of defect, Realistic outcomes, Teach signs/symptoms of infection, Sponge baths, don’t immerse in wate

24
Q

Teaching and s/s UTI in different ages

A

More common in girls – shorter urethra

CM: stomach ache
Infant: fussy, low grade fever
Wearing a diaper is susceptible
Potty training- UTI, bad perineal care

Tx: antibiotic

Prevention: frequent diaper changes, no bubble bath, avoid hot tubs and pools, drinking water, cranberry juice

25
AGN and Nephrotic syndrome: teaching/clinical manifestations/nursing care
``` AGN CM: Edema -- periorbital Anorexia Cola-colored urine Decreased urine output Pale, irritable, lethargic HA, abdominal discomfort, dysuria Increased BP hematuria ``` management: No specific treatment Recovery often spontaneous Supportive measures Hospitalization for substantial edema, hypertension, or significant oliguria Rest as needed Thorough assessments Assess urine volume, color, character Assess child’s appearance Assess behavior Advise family against bringing in salty foods, not to consume salty foods in front of child Divide amount of fluid allowed evenly and provide throughout the day Provide it in small cups to give the illusion of increased quantity Activity planning: need for frequent rest periods Infection prevention Frequent health supervision once/if at home (weekly to monthly) Assess BP every 4-6 hours Assess body weight daily Strict I/O Consider sodium and water restriction Dialysis for severe cases Medication Therapy: Loop diuretics i.e. furosemide, Calcium channel blockers, beta blockers, ACE inhibitors, Antibiotics, anti-convulsants if seizures are present Nutrition: Sodium restriction, Restrict foods with potassium if oliguria is present, Protein restriction for severe azotemia ``` Nephrotic Weight gain Edema Diarrhea, loss of appetite, malabsorption Decreased UO Urine is dark and frothy Pallor Skin breakdown Irritable Fatigue, lethargic Weight loss is often obscured by edema Nails are white Normal or decreased BP Susceptible to infection Goals: Reduce the excretion of urinary protein Maintain protein-free urine Prevent / treat acute infection Control edema Good nutrition (including protein, restrict salt) Corticosteroid therapy Prednisone daily for six weeks, then tapered for six weeks Expect improvement 7-21 days after initiating steroids Immunosuppressant therapy Indicated with frequent relapsing or steroid-resistant nephrotic syndrome Oral alkylating agent such as cyclophosphamide Loop Diuretics: Furosemide Plasma expander like human albumin Prognosis With early detection and prompt treatment, damage to membrane is minimal and full renal function is often restored Relapse ``` ``` Daily weight I/O Urine for albumin Abdominal girth Edema Skin condition Shock and infection Skin care Infection prevention Nutrition Diversion Family Anticipatory Guidance and Support ```
26
VUR care/medications/teaching
Prevent pyelonephritis!!! Conservative, non-operative therapy is effective in most cases High incidence of spontaneous resolution over time Low-dose antibacterial therapy with frequent urine cultures Surgery may be indicated with recurrent UTI’s, intolerance to antibiotics, noncompliance with therapy, or VUR after puberty in females Follow up ultrasounds post-operatively to evaluate renal growth
27
Enuresis management
``` Conditioning therapy Retention control training Waking schedule treatment Medication therapy (anticholinergic effect) Punishment is not treatment! Supportive therapy Child’s role Fluid restriction Behavior modification Patient education for the child and the parents ANTICIPATORY GUIDANCE Encouragement, patience and support Child’s active participation Side effects of medications Avoid diapering Positive reinforcement ```
28
Legg Calve Perthes vs Slipped Capital Epiphysis- presentation and treatment
SKFE Femoral head dislocates from the neck and shaft of the femur at the level of the epiphyseal plate Cause- mostly unknown!  Teen growth spurt Hormonal alterations Management Quick intervention is needed!! Screw inserted percutaneously into the femoral head Osteoarthritis may be a long term complication Legg-Calve-Perthes Avascular necrosis of the femoral head Most often children 4-8 years old, males more than females Patho Interruption of the blood supply to femoral head Swelling of soft tissue around the hip New blood vessels develop to provide the area with circulation allowing bone resorption and deposition 18-24 months for revascularization, more likely to fracture in this process. Over time the femoral head is reformed Treatment Anti-inflammatory meds Activity limitation Bracing, casting, or traction recommended Nursing implications Pain medications Education!! know how to properly place the brace and care for skin under the brace. Exercise of unaffected extremity is recommended. Treatment is based on severity of the disease. Sometimes no treatment except for avoiding contact sports. Often swimming and bicycling is recommending to help with range of motion without further damage.
29
Fractures in children and casting- process and complications
Clinical manifestations Swelling, bruising or redness, pain or tenderness Diminished functional use of affected part Muscular rigidity Crepitus Vascular injury Complications Circulatory impairment, nerve compression syndromes Physeal damage Nonunion, Malunion Infection, Pulmonary emboli 1. Observe nerve/circulation status closely 2. Reposition every 2 hours 3. Support wet cast with pillow & palm hand 4. Elevate extremity 5. Petal rough cast edges 6. No objects under cast 7. R.O.M. to extremity distal to cast 8. Restrict strenuous activity 9. Report foul odor, observe drainage 10. Clean soiled areas 11. Prepare for cast removal 12. Provide positive diversion and therapeutic play
30
JIA- medication adherence, treatment/cares
Pain Medications for inflammation Maintain joint range of motion without tension on the joints Splits or orthotics can be used, monitor skin for breakdown Psychosocial needs School Adequate sleep to minimize fussiness and non-compliance Support groups maintain weight
31
Hip Dysplasia- dx and treatment
assessment Trendelenburg Gait Trunk shifts over affected joint Ortolani Maneuver Abduct hips , listen and feel for a clunk Barlow Maneuver Adduct hips and feel for the femoral head slipping out ``` treatment Early detection is important! Pavlik Harness Keeps knees flexed and hips abducted to allow hips to grow normally Cares Do not adjust straps, only remove as directed Sleep on back Long socks and shirt under harness Call doctor with complications ```
32
Club Foot casting
Starts as soon after birth as possible Bracing, casting, or surgical release of soft tissue Once casted, skin assessment is important. Show parents how to assess temperature and cap refill of extremities when home as this will be an outpatient procedure if the child has no other problems. There will be pressure on the skin to move the foot into placement! Bones should be set before they start walking
33
Sickle Cell crisis: cause, manifestation, treatment, Hgb F
cause Diagnosed 3-4 months of age Individuals of African, Mediterranean, Middle Easter, and Indian decent Recessive genes for sickle cell are passed on from both parents who have the gene or trait Stress on the body can cause sickling: trauma, infection, fever, acidosis, dehydration, physical exertion, excessive cold exposure, or hypoxia. Blood gets viscous and starts to clump in small capillaries preventing normal blood flow. ``` manifestation Pain and clumping most often occurs in the joints, but can be anywhere in the body. Clumping in the lung capillaries leads to acute chest. This is a medical emergency. This leads to decreased gas exchange, producing hypoxia, which leads to further sickling. retinopathy/blindness avascular necoris splenomegaly hematuria ab pain dactylics osteomyelitis priapism anemia CHF ``` treatment aggressive hydration. They will get 2x maintenance fluids IV for the first few days. Once they start to have a decrease in pain we can change them to IV+PO. Narcotics- ED protocol and then PCA+basal rate IV fluids Antibiotics if febrile Hgb F decreased hgb- shorter cell life
34
Anemia
RBCs and Hgb are lower than normal ``` Causes Decreased production or RBCs Lack of dietary intake of nutrients needed to produce the cells Alterations in the cell structure Malfunctioning tissues (bone marrow) Toxin exposure (lead poisoning) Blood loss Genetic and cellulation development disorders ``` ``` iron deficiency anemia Lack of iron to produce hemoglobin Peak prevalence in children 6-24 months and puberty Causes Cow’s milk consumption 50% of iron in maternal milk is absorbed 10% of iron in cow’s milk is absorbed Assessment Health history Milk consumption Lack of supplementation Diet Chronic or acute blood loss Exam Fatigue, lethargy, pallor Safety Risk for changes in neuro function Unsteady gait related to dizziness Dietary interventions Infants fed only iron fortified formula Breast fed infants to start on supplementation at 4-5 months Limit milk to 24oz per day Education on iron rich foods Picky eaters Supplementation Proper iron fortified diet Oral or IV supplement Blood transfusions Oral care Stool softeners ```
35
Hemophilia injury management/treatment
TREAT THE BLEED Treat with RICE REST—immobilize for comfort and to prevent further bleeding ICE—apply cold to promote vasoconstriction COMPRESSION—pressure to encourage clot formation ELEVATION—elevate joint Gentle active ROM Only after bleeding stopped—within 24 to 48 hours Allow client to control own pain tolerance DO NOT do passive exercise Could stretch joint capsule Could cause bleeding with acute episode ``` Management Prevention Factor replacement NEVER THROW FACTOR AWAY! HIV Education ```
36
Diagnostic procedures for oncologic processes: nurses role
treat side effects of chemo labs: Labs drawn and focused on will be determined by the suspected dx, same with radiology. A common practice when cancer is suspected is a chest xray to look for mediastinal mass. If this child with a mass is sedated and they are unable to maintain their airway, we have a serious emergency!! radiology procedures: bone marrow aspirate or biopsy as well as lumbar puncture. Biopsy of the tumor: would dictate and pre-op and post-op cares for the nurse. education Scared!! Lots of teaching and hands on practice with central lines When to be alarmed Temp of 101 or greater (or climbing) Cough or rapid breathing Oozing gums, nose bleed lasting longer than 10 minutes Lethargic, fatigue Ear, head, neck ache (nuchal rigidity) Problems with central line: broken, red/sore Abdominal pain, problems eating
37
Symptoms at diagnosis: leukemia, retinoblastoma, neuroblastoma, wilm’s
leukemia: bone pain metastasis to blood, bone, CNS, spleen, liver or more ``` retinoblastoma: Cat Eye reflex Strabismus Red, painful eye, often with glaucoma Blindness (late sign) ``` neuroblastoma: Swollen/asymmetric abdomen Bowel and bladder dysfunction Bruising of the eyes Wilm's: Swelling, mass in abdomen R/T compression: HTN, hematuria, wt loss, fever, mets to lungs
38
Neutropenia
risk for infection | low WBC, neutrophil count
39
ANC calculation
ANC= Bands+Segs (or Neutrophils) x WBC(10) | < 500 neutropenic
40
Parental characteristics, common characteristics of abused children
social isolation poor support system parental low self-esteem & less adequate maternal functioning Alcohol abuse (caregiver)—The compulsive use of alcohol that is not of a temporary nature. Drug abuse (caregiver)—The compulsive use of drugs that is not of a temporary nature. Financial problem (caregiver)–A risk factor related to the family’s inability to provide sufficient financial resources to meet minimum needs. Inadequate housing (caregiver)–A risk factor related to substandard, overcrowded, or unsafe housing conditions, including homelessness. compatibility between child & parents temperament and parents ability to deal with behavioral style
41
abuse prevention
Child Abuse Prevention and Treatment Act (CAPTA) provides funds to states to improve CPS systems assist states with screening and investigating child abuse and neglect report child protective services (MO) department of children & families (KS)
42
reporting child abuse
When in doubt, report. Worst case scenario, it was nothing and a social worker visit the house. Best case scenario, you save lives!!!! And break cycles!!! mandatory reporter
43
abuse in different cultures
Cupping, coining, Eastern medicine practices used that could appear to be abuse goal: Better circulation, helps lymphatic system
44
Understanding of concept of death
Infant Unconditional love and trust Ensure family is available to the child Toddler (1-3 yo.) Familiarity and routine Maximize time with parents, bring in items from home Child (3-5 yo.) Death is punishment for wrong doing, correct this misunderstanding Use precise language Help family express that they will miss the child and will continue to function when they are gone School age (5-10 yo.) Concrete understanding of death Need specific honest details Encourage to help with decisions Young adolescent (10-14 yo.) Benefits from reinforcement of self-esteem Respect privacy and need for peers Support the need for independence and decision making Older teen (14-18 yo.) Adult-like understanding Needs support through honest, detailed explanations and need to be heard!
45
Family centered care
Honesty with parents and child (as developmentally appropriate) Clarify and answer questions No judgment Sensitive to ethnic, spiritual, or cultural preferences assure change in focus to pain control & comfort