Thursday, February 26, 2009

Pediatric Nursing: Respiratory Disorders 2

Pneumonia
An inflammatory condition of the lungs

in which alveoli fill with fluid or blood

resulting in poor oxygenation and air

exchange.


Symptoms
High fever
Thick green, yellow, or blood tinged secretions
Grunting respirations
Rales, crackles, diminished breath sounds
Cough and cyanosis
Infiltrate seen on x-ray


Management
Assess for respiratory distress
NPO (rr > 60 = high risk for aspiration)
IV fluids
Oxygen as need to keep oxygen saturation above 95%
CPT
Deep suctioning
Acetaminophen for fever / antibiotics


Pneumonia Isolation
Respiratory isolation
May be taken off isolation if RSV negative and on antibiotics for 24 hours.


Pathophysiology: Cystic Fibrosis
A chronic, progressive, genetic illness involving the digestive system and lungs.
Abnormality of the exocrine glands
Sweat and mucous glands
Mucus of CF is thick and viscous
Causes scar tissue
Leads to irreversible lung damage


Exocrine Gland Dysfunction
Mucous secretions are thick and tenacious
Dysfunction of mucous producing glands leads to multiple gastrointestinal absorption problems.
Blocked pancreatic ducts
No secretion of digestive enzymes


Symptoms
Meconium ileus at birth
Failure to thrive
Steatorrhea stools / constipation
Voracious appetite with poor weight gain
Recurrent respiratory infections
Chronic cough
Malabsorption of intestines

Diagnosis
Positive sweat test
Genetic marker
Life long management
Enzyme replacement with eating
Daily CPT postural drainage
Inhaled bronchodilators
Control of lung infections
Nutritional supplements as needed



Medications
Enzymes to help digest food
Antibiotics to control infection
Bronchodilators to open airways
Vitamin C to improve absorption of other meds
Vitamins E, A, D, K / fat soluble vitamins


Long Term Complications
Nasal polyps
Sinusitis
Rectal polyps / prolapse
Hyperglycemia / diabetes
infertility


Asthma
Asthma is a chronic, inflammatory lung disease involving recurrent breathing problems.
Caused by complex, multicellular reaction in the airway characterized by:
Airway inflammation
Airway hyper-responsiveness to a variety of triggers


Symptoms
Wheezing
Cough
Tightness of chest
Prolonged expiratory phase
Hypoxemia
X-ray = hyper-expansion of lungs



Medical Management
High fowlers position / bed rest
Pulse oximetry
Nebulized albuterol
CPT
Methylprednisone / Solu-medrol IV
IV fluids
Oxygen to keep oxygen sats > 95%


Home Management
Peak flow spirometer
Identify triggers
Maximize lung function
Optimal physical growth
Optimal psycho-social state
Maximum participation


Peak Flow Monitoring

  • Spirometry measures how
    much and how fast air is
    forcefully expelled from fully
    inflated lungs.

  • Recommended standard of care
    for management of asthma.


Home Medications
Rescue drugs: short acting albuterol beta 2 agonist – used as a quick-relief agent for acute bronchospasm and for prevention of exercise induced bronchospasm.
Anti-inflammatory or preventative: low-dose inhaled corticosteroid: inhaled or oral prednisone
Allergy: Singulair


Bronchodilators
Bronchodilators rapidly relax the airway smooth muscle cells, thus reversing the bronchospasm until anti-inflammatory effect of steroids is attained.
Aerosols
Via mouth piece 3 years and older
Via facial mask for less than 3 years


Corticosteroids
Steroids reduce the inflammatory component of bronchial obstruction, decrease mucus production and mediator release, as well as the late phase (cellular) inflammatory process.
Methyl prednisone IV in severe cases
May need Reglan if experiencing GI upset
PO prednisone – always give with food to decrease GI upset


Anti-inflammatories
Oral prednisone (Pedia-pred, Prelone, Liquid pred) recommended for short course in moderate or severe exacerbation
Inhaled: Pulmicort, AeroBid, Flovent
Infant: mask should fit firmly: cataracts
Older child: rinse and spit after treatment to prevent thrush


Family Teaching:
Teach how to use medication
When to use and how often
No OTC drugs
Increase fluid intake
Signs and symptoms of respiratory distress



Bronchopulmonary Dysplasia


History
It occurs in newborns who are born prematurely and or have a variety of pulmonary disorders and who require ventilatory support with high pressure and oxygen in the first 2 weeks of life.


Pathophysiology
Fibrosis of airways and marked hyperplasia of the bronchial epithelium
Increased fluid in the lungs, as a result of disruption of the alveolar-capillary membrane
Over distention due to damage to alveolar supporting structures resulting in air trapping
Fibrosis, airway edema, and broncho-constriction


BPD Symptoms
Persistent respiratory distress
Dependent on supplemental oxygen
Failure to thrive
Gastro-esophageal reflux
Pulmonary hypertension


Long Term Management
Supplemental oxygen
CPT
Bronchodilators
Diuretics (pulmonary hypertension)
Anti-inflammatory medication
Nutritional support: po formula + NG supplement
Gastrostomy tube (GER)
Bicarbonate in formula due to chronic state of acidosis


Long-term Outcomes
Oxygen dependent
Visual problems
Feeding difficulties
Developmental delay
Learning difficulties





Pediatric Nursing: Respiratory Disorders

Pediatric Nursing: Respiratory Lecture notes


Upper Airway Characteristics
Narrow tracheo-bronchial lumen until age 5
Tonsils, adenoids, epiglottis proportionately larger in children
Tracheo-bronchial cartilaginous rings collapse easily


Lower Airway Characteristics
Fewer alveoli in the neonate
Poor quality of alveoli until age 8
Lack of surfactant that lines the alveoli in the premature infant
Inhibits alveolar collapse at end of expiration

Respiratory Characteristics
Basal metabolic rate is greater thus greater oxygen consumption
Immunoglobulin G (IgG) levels reach low point around 5 months of age


Focused Physical Assessment
Types of breathing:
Less than 7 years abdominal breathing
Greater than 7 years abdominal breathing can indicate problems


Respiratory Rate
Inspiratory phase slightly longer or equal to expiratory phase
Prolonged expiratory phase = asthma
Prolonged inspiratory phase = upper airway obstruction
Croup
Foreign body


Color
Observe color of face, trunk, and nail beds
Cyanosis = inadequate oxygenation
Clubbing of nails = chronic hypoxemia


Respiratory Distress
Grunting = impending respiratory failure
Severe retractions
Diminished or absent breath sounds
Apnea or gasping respirations
Poor systemic perfusion / mottling
Tachycardia to bradycardia = late sign
Decrease oxygen saturations


Chest Retractions
Retractions suggest an obstruction to inspiration at any point in the respiratory tract.
As intrapleural pressure becomes increasingly negative, the musculature "pulls back" in an effort to overcome the blockage.
The degree and level of retraction depend on the extent and level of the obstruction.

Diagnostic Tests
Detects abnormalities of chest or lungs
Chest x-ray
Sweat chloride Test
MRI
Laryngoscope / bronchoscopy
CT Scan


Sweat Chloride Test
•Analysis of sodium and chloride
•Contents in sweat
•Gold Standard for diagnosis
•May do genetic screening earlier
if positive family history

Foreign Body
A foreign body in one
or the other of the bronchi
causes unilateral
retractions.
*usually the right due to
broader bore and more
vertical placement.


Oxygen Therapy: Nursing Interventions
Proper concentration
Adequate humidity: make sure there is fluid in the bottle
Make sure prongs are in nose and that the nares are patent – suction out nares to increase oxygen flow
Monitor oxygen SATS: if alarm keeps on going off but the infant / child looks good, check the device
Monitor activity level or infant / child



Aerosol Therapy
Respiratory Therapist will do the treatment
Communicate with therapist – eliminated needless paging for treatments
Treatment should be done before the infant eats
When you make your morning rounds assess if there is any infant / child that needs an immediate treatment


Home Teaching Inhaled Medications
Correct dosage
Prescribed time
Proper use of inhaler
No OTC drugs
Encourage fluids
When to call physician


Aerosol Therapy
Nebulizer - infant

Outpatient Aerosol Treatment
Mechanical Ventilation

CPT
In the small child you can position on your lap
Do first thing in the AM
Do before meals or one hour after
Do after the aerosol treatment since the treatment will help open the airways and loosen the mucous
Suction the infant after treatment – teach parents to do bulb suction – RN, LVN or RT to deep suction prn


Severe Respiratory Distress
Nasal flaring and grunting
Severe retractions
Diminished breath sounds
Hypotonia
Decreased oxygen saturations


What to do if infant / child in respiratory distress!
Stimulate the infant / child - remember crying or activity will help mobilize secretions and expand lungs
Have the older child sit up take deep breaths and cough
CPT to loosen secretions and suction! suction! suction!
Give oxygen
Assess if interventions work
Call for help if you need it – pull the emergency cord – yell for help


Allergic Rhinitis
Symptoms
Itching of nose, eyes, and throat
Sneezing and stuffiness
Watery nasal discharge / post nasal drip
Watery eyes
Swelling around the eyes


Rhinitis Treatment
Antihistamines
Competitive inhibitors for histamine at the mast cell receptor sites
Benadryl – OTC medication
Prescription –Cromolyn or steroid nasal spray
Environmental changes - avoidance of allergens
Do not use combination OTC medications especially those that contain pseudoephedrine

Sinusitis Symptoms
Fever
Purulent rhinorrhea
Pain in facial area
Malodorous breath
Chronic night-time cough


Treatment
Normal saline nose drops
Warm pack to face
Acetaminophen for pain
Increase po fluid intake
Antibiotics
Recent studies question their effectiveness


Tonsillitis
Inflammation of the tonsils.
Part of the immune system to trap and kill bacteria and viruses traveling through the body.

Tonsillitis
Child may refuse to drink
Night snoring = enlarged tonsils or adenoids
Size of tonsils are obstructing airway


Treatment
Antibiotics x ten days if positive for beta strep
Acetaminophen for pain
Cool fluids
Saline gargles
Antiseptic sprays
Viral throat infections will not get better faster with antibiotics.


Tonsillectomy
Done if child’s respiratory status is compromised
Post operative care:
Side lying position
Ice collar
Watch for swallowing
Cool fluids / soft diet


Croup
Laryngotracheobronchitis or Acute spasmotic croup
Infants from 3 months to about 3 years
Respiratory symptoms are caused by inflammation of the larynx and upper airway, with resultant narrowing of the airway.

Symptoms
Symptoms:
Hoarseness
Inspiratory stridor
Barking cough
Afebrile
Often worsens at night


Management
Home care:
Cool mist
Fluids
Hospital care:
Racemic epinephrine inhalant
Mist tent – not used much anymore
Dexamethasone: IV over 1 to several minutes


Pertussis or whooping cough
Agent: Bordetella Pertussis
Source: respiratory
Transmission: droplet
Incubation: 10 days
Period of communicability: before onset of paroxysms to 4 weeks after onset


Management
Respiratory support as needed
Suctioning
Oxygen to keep oxygen saturation at > 98 %
Nutritional support
IV fluids
Erythromycin, Zithromax or Biaxin for child and all exposed family members

Isolation Precautions
Transmission through direct contact with discharges from respiratory mucous of infected persons.
Highly contagious with up to 90% of household contacts developing disease after contact.
Respiratory and contact isolation for 3-4 days after the initiation of antibiotic therapy.


Epiglottitis Symptoms
Acute inflammation of supra-glottic structures.
Medical Emergency
Sudden onset
High fever
Dysphasia and drooling
Epiglottis is cherry red and swollen


Epiglottitis
Has decreased dramatically since introduction of the Haemophilus influenzae type b or Hib vaccine in 1985.
Incidence as of 2003: 32 cases in children under 5 years of age.
Incidence in the adult population has increased from 0.8 to 3.1 per 100,000 adults


Management
Diagnosis made on presenting symptoms
No tongue blade in mouth
Emergency tracheostomy set
No procedures until in the operating room
Keep quiet
Ceftriaxone – third-generation cephalosporin for 7 to 10 days.


Apnea
Apnea is cessation of respiration lasting longer than 20 seconds.
Monitor in hospital for 48 hours for underlying problems.
Discharge home with monitor


Foreign Body
Severe inspiratory stridor
Symptoms depend on location
Unilateral chest movement
Chest x-ray
Bronchoscope to remove object

Teaching
No small hard candies, raisins, popcorn or nuts until age 3 or 4 years
Cut food into small pieces
No running, jumping, or talking with food in mouth
Inspect toys for small parts
Keep coins, earring, balloons out of reach


Influenza
Associated with community epidemic
Febrile, URI, achy joints,
Management:
Acetaminophen for fever
Fluids
Keep away from others
Watch for signs of pneumonia


Bronchiolitis
Acute obstruction and inflammation of the bronchioles.
Most common causative agent: RSV
Respiratory syncytial virus
Bronchioles become narrowed or occluded as a result of inflammatory process, edema, mucus and cellular debris clog alveoli


Symptoms
Harsh dry cough
Low grade fever
Feeding difficulties
Wheezing
Respiratory distress with apnea
Thick mucus


Management
Oxygen to maintain oxygen saturation >than 95%
Pulse oximeter
Normal saline nose drops before suctioning
Deep suction especially before feeding
CPT to mobilize secretions
Inhalation therapy – not sure it is beneficial
Mechanical ventilation as needed


RSV Positive - Isolation
RSV is spread from respiratory secretions through close contact with infected persons or contact with contaminated surfaces or objects.
Patient should be on contact and respiratory isolation
Can be placed with other RSV + patients




Tuesday, February 24, 2009

Alteration in Fluid and Electrolyte Status Lecture notes

Fluid and Electrolytes
Alteration in Fluid and Electrolyte Status Lecture notes

Developmental and Biological Variances
 Infants younger than 6 weeks do not produce tears.
 In an infant a sunken fontanel may indicate dehydration.
 Infants are dependant on others to meet their fluid needs.
 Infants have limited ability to dilute and concentrate urine.

Developmental and Biological
 The small the child, the greater the proportion of body water to weight and proportion of extracellular fluid to intracellular fluid.
 Infants have a larger proportional surface are of the GI tract than adults.
 Infants have a greater body surface area and higher metabolic rate than adults.
Water Balance
 Regulated by Anti-diuretic Hormone ADH.
 Acts on kidney tubules to reabsorb water.
 The young infant is highly susceptible to dehydration.

Increased Water Needs
 Fever
 Vomiting and Diarrhea
 High-output in renal failure
 Diabetes insipidus
 Burns
 Shock
 Tachypnea

Decreased Water Needs
 Congestive Heart Failure
 Mechanical Ventilation
 Renal failure
 Head trauma / meningitis

General Appearance
 How does the child look?
 Skin:
• Temperature
• Dry skin and mucous membranes
• Poor turgor, tenting, dough-like feel
• Sunken eyeballs; no tears
• Pale, ashen, cyanotic nail beds or mucous membranes.
• Delayed capillary refill > 3 seconds
Loss of Skin Elasticity

Cardiovascular
 Pulse rate change:
 Note rate and quality: rapid, weak, or thready
 Bounding or arrhythmias
 Tachycardia #1 sign that something is wrong
 Increased HR may be first subtle sign of hypovolemia
 Blood Pressure
 Note increase or decrease (remember it takes a 25% decrease in fluid or blood volume for change to occur)
Respiratory
 Change in rate or quality
 Dehydration or hypovolemia
 Tachypnea
 Apnea
 Deep shallow respirations
 Fluid overload
 Moist breath sounds
 Cough

Diagnostic Tests
 Make sure free flowing specimen is obtained, a hemolyzed or clotted specimen may give false values.
Hemoglobin and Hematocrit
 Measures hemoglobin, the main component of erythrocytes, which is the vehicle for transporting oxygen.
 Hgb and hct will be increased in extracellular fluid volume loss.

 Hgb and hct will be decreased in extracellular fluid volume excess.
Electrolytes
 Electrolytes account for approximately 95% of the solute molecules in body water.
 Sodium Na+ is the predominant extracellular cation.
 Potassium K+ is the predominant intracellular cation.

Potassium
 High or low values can lead to cardiac arrest.
 With adequate kidney function excess potassium is excreted in the kidneys.
 If kidneys are not functioning, the potassium will accumulate in the intravascular fluid
Potassium
 Adults: 3.5 to 5.3 mEq /L
 Child: 3.5 to 5.5 mEq / L
 Infant: 3.6 to 5.8 mEq / L

 Panic Values:
<> 7.0 mEq / L

Hyperkalemia
 Defined as potassium level above 5.0 mEq / L
 Significant dysrhythmias and cardiac arrest may result when potassium levels arise above 6.0 mEq/L
 Adequate intake of fluids to insure excretion of potassium through the kidneys.

CM: Hyperkalemia
 Nausea
 Irregular heart rate
 Pulse slow / irregular
Causes of Hyperkalemia
 Acute renal failure
 Chronic renal failure
 Glomerulonephritis

Diagnostic tests:
 Serum potassium
 ECG
 Bradycardia
 Heart block
 Ventricular fibrillation

Hypokalemia
 Potassium level below 3.5 mEq / L
 Before administering make sure child is producing urine.
 A child on potassium wasting diuretics is at risk – Lasix
CM: Hypokalemia
Neuromuscular manifestations are: neck flop, diminished bowel sounds, truncal weakness, limb weakness, lethargy, and abdominal distention.

Causes of Hypokalemia
 Vomiting / diarrhea
 Malnutrition / starvation
 Stress due to trauma from injury or surgery.
 Gastric suction / intestinal fistula
 Potassium wasting diuretics
 Ingestion of large amounts of ASA

Foods high in potassium
 Apricots, bananas, oranges, pomegranates, prunes
 Baked potato with skin, spinach, tomato, lima beans, squash
 Milk and yogurt
 Pork, veal and fish
Monitor Potassium Levels

Sodium
 Sodium is the most abundant cation and chief base of the blood.
 The primary function is to chemically maintain osmotic pressure and acid-base balance and to transmit nerve impulses.
 Normal values: 135 to 148 mEq / L

Hyponatremia
 Reflects an abnormal rate of sodium to water and is defined as a serum sodium concentration less than 135 mEq/L.
 Results from retention of water secondary to impairment in free water excretion.

Pathophysiology
 When sodium levels drop in the fluids outside the cells, water will sweep into the cells in an attempt to balance the concentration of salt outside the cells.
 Cells will swell as the result of the excess water.
 Brain cells cannot accommodate – symptoms of hyponatremia result from brain swelling

Diagnosis
 10 to 15% of patients
 Vomiting, diarrhea, or excessive sweating
 Vital Signs: BP (orthostatic), skin turgor, mucous membrane appearance, jugular vein distention, edema
 Lab values
 History of oral intake of low-electrolyte or electrolyte free fluids

Early Manifestations
 Anorexia, nausea, lethargy and apathy
 More advanced symptoms: disorientation, agitation, seizures, depressed reflexes, focal neurological deficits
 Severe: coma and seizures: sodium concentration less than 120 mEq/L
Medical Management
 Normal saline given as resuscitative fluid
 May need to reduce the fluid rate to 75% of maintenance
 Supplemental oxygen
 Water and salt restrictions

Hypernatremia
 Serum sodium greater than 150 mEq/L is caused by conditions that produce an excessive gain of sodium or excessive loss of water that is greater than the loss of sodium.
Clinical Pearl
 Most infant with severe dehydration have a history of lethargy, listlessness, and decreased responsiveness; those with hypernatremia dehydration tend to be irritable and fussy.

Hypernatremia
 Inadequate fluid intake – 75%
 Gastrointestinal losses – 44%
 Occurs primarily in infants with diarrhea dehydration
 Diabetes insipidus was major reason for excessive urinary output
 Loss from high fever, environmental temperatures and hyperventilation

Primary Sodium Excess
 Improperly mixed formula or re-hydration solution
 Ingestion of sea water
 Hypertonic saline IV
 High breast milk sodium

Primary Water Deficit
 Diabetes Insipidus
 Diabetes Mellitus
 Gastroenteritis (water loss greater than solute loss)
 Inadequate breast feeding
 Withholding of water: handicapped
 Increased insensible loss – premature infant

Treatment Modalities
Intraosseous Therapy
Central Venous Catheter

Total Parental Nutrition
TPN Therapy
 TPN provides complete nutrition for children who cannot consume sufficient nutrients through gastrointestinal tact to meet and sustain metabolic requirements.
 TPN solutions provide protein, carbohydrates, electrolytes, vitamins, minerals, trace elements and fats.

Complications of TPN
 Sepsis: infection
 Liver dysfunction
 Respiratory distress from too –rapid infusion of fluids
TPN: care reminder
caREminder:
 The TPN infusion rate should remain fairly constant to avoid glucose overload. The infusion rate should never be abruptly increased or decreased.

Dehydration
General Assessment
 Loss of weight
 Level of consciousness
 Alert to irritable
 Restless to lethargic
 Lethargic to coma
Skin Turgor
 In moderate dehydration the skin may have a doughy texture and appearance.

 In severe dehydration the more typical “tenting” of skin is observed.
Skin Turgor

Urine Output
 Normal urine output is 1-2 mL/kg/hr
 In mild dehydration urine output may be low – parent may report decrease in voiding
 Moderate dehydration urine output would be low and concentrated (oliguric) with elevated specific gravity.
 Severe dehydration would by (anuric) very low – very concentrated urine with high S.G.

Vital Signs
 The heart rate is the most sensitive indicator of dehydration / hypovolemia.
 HR will be elevated in an attempt to compensate for fluid loss.
 Blood pressure will only drop as child is severely dehydrated (>10%).
Treatment of Mild to Moderate
 ORT – oral re-hydration therapy
 50 ml / kg every 4 hours
 Increase to 100 ml / kg every 4 hours
 Non carbonated soda, jell-o, fruit juices or tea.
 Commercially prepared solutions are the best.

Re-hydration Therapy
 Increase po fluids if diarrhea increases.
 Give po fluids slowly if vomiting.
 Stop ORT when hydration status is normal
 Start on BRAT diet
 Bananas
 Rice
 Applesauce
 Toast


Teaching / Parent Instruction
 Call PMD
 If diarrhea or vomiting increases
 No improvement seen in child’s hydration status.
 Child appears worse.
 Child will not take fluids.
 NO URINE OUTPUT

Moderate to Severe Dehydration
Fluid replacement

 Isotonic fluids initially:

 Normal Saline 0.9%
 Followed by: Dextrose 5% in.45 NS

Potassium is added only after child has voided.

Nursing Interventions
 Assess child’s hydration status
 Accurate intake and output
 Daily weights
 most accurate way to monitor fluid levels
 Hourly monitoring of IV rate and site of infusion.
 Increase fluids if increase in vomiting or diarrhea.
 Decrease fluids when taking po fluids or signs of edema.

Care Reminder
 A severely dehydrated child will need more than maintenance to replace lost fluids. 1 ½ to 2 times maintenance.
 Adding potassium to IV solution.
 Never add in cases of oliguria / anuria
• Urine output less than 0.5 mg/kg/hour
 Never give IV push
 Double check dosage

Over hydration
 Occurs when child receives more IV fluids that needed for maintenance.
 In pre-existing conditions such as meningitis, head trauma, kidney shutdown, nephrotic syndrome, congestive heart failure, or pulmonary congestion.

Signs and Symptoms
 Tachypnea
 Dyspnea
 Cough
 Moist breath sounds
 Weight gain from edema
 Jugular vein distention
Safety Precautions
 Use small bags of fluid or buretrol to control fluid volume.
 Check IV solution infusion against physician orders.
 Always use infusion pump so that the rate can be programmed and monitored.
 Even mechanical pumps can fail, so check the intravenous bag and rate frequently.
 Record IV rate q hour

Acid – Base Imbalances
Acidosis:
 Respiratory acidosis is too much carbonic acid in body.
 Metabolic Acidosis is too much metabolic acid.
Alkalosis.
 Respiratory alkalosis is too little carbonic acid.
 Metabolic alkalosis is too little metabolic acid.
Respiratory Acidosis
 Caused by the accumulation of carbon dioxide in the blood.
 Acute respiratory acidosis can lead to tachycardia and cardiac arrhythmias.
Causes of Respiratory Acidosis
 Any factor that interferes with the ability of the lungs to excrete carbon dioxide can cause respiratory acidosis.
 Aspiration, spasm of airway, laryngeal edema, epiglottitis, croup, pulmonary edema, cystic fibrosis, and Bronchopulmonary dysplasia.
 Sedation overdose, head injury, or sleep apnea.

Medical Management
 Correction of underlying cause.
 Bronchodilators: asthma
 Antibiotics: infection
 Mechanical ventilation
 Decreasing sedative use.
Respiratory Alkalosis
 Occurs when the blood contains too little carbon dioxide.
 Excess carbon dioxide loss is caused by hyperventilation.
Causes of hyperventilation

 Hypoxemia
 Anxiety
 Pain
 Fever
 Salicylate poisoning: ASA
 Meningitis
 Over-ventilation

Management
 Stress management if caused by hyperventilation.
 Pain control.
 Adjust ventilation rate.
 Treat underlying disease process.

Metabolic Acidosis
 Caused by an imbalance in production and excretion of acid or by excess loss of bicarbonate.
Causes:
 Gain in acid: ingestion of acids, oliguria, starvation (anorexia), DKA or diabetic ketoacidosis, tissue hypoxia.
 Loss of bicarbonate:
diarrhea, intestinal or pancreatic fistula, or renal anomaly.

Ingestion of large doses of Aspirin
Management
 Treat and identify underlying cause.
 IV sodium bicarbonate in severe cases.
 Assess rate and depth of respirations and level of consciousness.

Metabolic Alkalosis
 A gain in bicarbonate or a loss of metabolic acid can cause metabolic alkalosis.
Causes:
 Gain in bicarbonate:
Ingestion of baking soda or antacids.
Loss of acid:
Vomiting, nasogastric suctioning, diuretics massive blood transfusion

Clinical Manifestations
 Hypertonicity or tetany
 Management: Correct the underlying condition

Friday, February 6, 2009

Things to note: Digoxin in Pediatrics

  1. You must always check apical pulses in Kids before giving Digoxin
  2. If they are bradycardic hold the Digoxin and call the physician
    < 100 beats / min for infant and toddler
    < 80 beats in the older child
    < 60 beats in the adolescent
  3. Teach parents signs of Digoxin toxicity which includes vomiting in children and sight alteration(double vision) which babies cannot tell you but older kids may be able to tell you.
  4. Digoxin must be given when due, if a dose is missed call the physician
  5. Digoxin cannot be made up if for example the child throws up after you give the med, you have to call the doctor
  6. Digoxin toxicity can occur when taking lasix as well why? Because lasix depletes pottassium which gives Digoxin more receptors to bind to hence rendering it toxic.

Thursday, February 5, 2009

Pediatric Nursing Cardiac Diseases


  • Lecture notes on Pediatric Cardiac Diseases

    Health History
    Family history of defects / early cardiac disease / siblings with defects
    Maternal history of stillborns or miscarriages
    Congenital anomalies / genetic anomalies / fetal alcohol syndrome / Down Syndrome and Turner Syndrome
    Maternal exposure to rubella



    Present Health History
    Heart murmur
    Tires while eating
    Low weight for height
    Sweats while eating (diaphoretic)
    Cyanosis, worsens with feeding or activity level
    Irritable weak cry


    Health History
    In the older child additional symptoms may include:
    Chest pain
    Decreased activity level
    Syncope
    Slight of build


    Heart Sounds
    Use both the bell (for low frequency) and the diaphragm (for high frequency)
    Quality: distinct S1 and S2
    Rate matches radial pulse
    Intensity
    Rhythm



    Heart Sounds
    Heart sounds should be crisp and distinct in children.
    S1 is the first heart sound, produced by closure of the tricuspid and mitral valves when ventricular contraction begins.
    S2 is produced by the closure of the aortic and pulmonic valves.



    Heart Murmurs
    These sounds are produced by blood passing through a defective valve, great vessel, or other heart structure.
    Murmurs are classified by: intensity, location, radiation, timing, and quality.



    Knee-chest Position (TET spells)

    Children with cyanotic heart
    defect squat (assumes a knee-chest position) to relieve
    cyanotic spells. Some times called “tet” spells.
    Nurses put infant in knee-chest
    position. This positioning decreases blood return from the lower extremities.



    First Breath
    Pulmonary alveoli open up
    Pressure in pulmonary tissues decreases
    Blood from the right heart rushes to fill the alveolar capillaries
    Pressure in right side of heart decreases
    Pressure in left side of heart increases
    Pressure increases in aorta



    Treatment Modalities
    Palliative procedures
    Pulmonary artery banding
    Shunts
    Corrective procedures


    Diagnostic Test
    Chest x-ray to define silhouette of the heart.
    Heart size, shape, pulmonary markings, and cardiomegaly.
    Electrocardiogram to define electrical activity of the heart.
    Echo-cardiogram to visualize anatomic structures.
    Cardiac Conduction

    Cardiac Catheterization
    An invasive test to diagnose or treat cardiac defects.
    Visualizes heart and vessels.
    Measures oxygen saturation of chambers.
    Measures intra-cardiac pressures.
    Determines muscle function and pumping action of the heart.

    Pre-cardiac Catheterization
    Assess vital signs with blood pressure.
    Hemoglobin and hematocrit
    Pedal pulses
    NPO
    Hold digoxin
    IV if child is polycythemic

    Post-cardiac Catheterization
    Vital sign, with apical pulse, and blood pressure q 15 minutes for first hour.
    Apical pulse for 1 minute to check for bradycardia or dysrhythmias.

    Toxicity to Dye
    Watch for signs of toxicity to the dye used during the procedure.
    Increased temperature
    Urticaria
    Wheezing
    Edema
    Dyspnea
    Headache

    Home Care Instructions
    Keep dressing in place for 24 hours.
    Keep site dry and clean.
    Observe site for redness, swelling, drainage, or bleeding.
    Check temperature.
    Avoid strenuous exercise.
    Acetaminophen for pain.
    Keep follow-up appointment
    Pre-procedure medications as ordered.
    Post-cardiac Catheterization
    Assess pulses below the cath site.
    Record quality and symmetry of pulses.
    Assess temperature and color of affected extremity.
    Check dressing for bleeding or hematoma formation.

    Right to Left Shunts
    Occurs when pressure in the right side of the heart is greater than the left side of the heart.
    Resistance of the lungs in abnormally high
    Pulmonary artery is restricted
    Deoxygenated blood from the right side shunts to the left side
    Hole in septum + obstructive lesion =
    Deoxygenated blood from the right side of the heart shunts to the left side of the heart and out into the body.

    Clinical Manifestations
    Hypoxemia = the result of decreased tissue oxygenation.
    Polycythemia = increased red blood cell production due to the body’s attempt to compensate for the hypoxemia.
    Increase viscosity of the blood = heart has to pump harder.
    Potential Complications
    Thrombus formation due to sluggish circulation.
    Brain abscess or stroke due to the un-oxygenated blood bypassing the filtering system of the lungs.

    Left to Right Shunt
    Pressures on the left side of the heart are normally higher than the pressures in the right side of the heart. If there is an abnormal opening in the septum between the right and left sides, blood flows from left to the right.

    Clinical Manifestations
    The infant is not cyanotic.
    Tachycardia due to pushing increased blood volume.
    Cardiomegaly due to increased workload of the heart.
    Dyspnea and pulmonary edema due to the lungs receiving blood under high pressure from the right ventricle.
    Increased number of respiratory infections due to blood pooling in the the lungs promoting bacterial growth.

    Congestive Heart Failure
    Major manifestation of cardiac disease.
    Under 1 year of age due to congenital anomaly.
    Over 1 year with no congenital anomaly may be due to acquired heart disease.
    Cardinal Signs of CHF
    Tachycardia
    Cardiomegaly
    Tachypnea
    Hepatomegaly

    Digoxin Therapy

    nDigoxin increases the force of the myocardial contraction.
    qTake an apical pulse with a stethoscope for 1 full minute before every dose of digoxin. If bradycardia is detected.
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* Call physician before administering the drug.

Patent Ductus Arteriosus
PDA
Incidence 10%
One of the most common benign defects
Ductus normally closes within hours of birth
Connection between the pulmonary artery (low pressure) and aorta (high pressure)
High risk for pulmonary hypertension

Diagnosis and Treatment
Diagnosis: heart murmur may be heard in the pulmonary valve area because the heart is forcing an unusually large amount of blood through a normal sized valve.
Echocardiogram is the primary method used to diagnose the defect – it can show the hole and its size and any enlargement of the right atrium and ventricle in response to the extra work they are doing.


Treatment
Surgical closure of the atrial septal defect
After closure in childhood the heart size will return to normal over a period of four to six months.
No restrictions to physical activity post closure


Ventricular Septal Defect
VSD
30% of defects
Opening in the ventricular septum
Left-to-right shunt
Right ventricular hypertrophy
Deficient systemic blood flow
VSD
Small holes generally are asymptomatic
Medium to moderate holes will cause problems when the pressure in the right side of the heart decreases and blood will start to flow to the path of least resistance (from the left ventricle through the VSD to the right ventricle and into the lungs)
This will generally lead to CHF


Diagnosis and Treatment
Diagnosis – heart murmur – clinical pearl a louder murmur may indicate a smaller hole due to the force that is needed for the blood to get through the hole.
Electrocardiogram – to see if there is a strain on the heart
Chest x-ray – size of heart
Echocardiogram – shows size of the hole and size of heart chambers


Treatment VSD
CHF: diuretics of help get rid of extra fluid in the lungs
Digoxin if additional force needed to squeeze the heart
FTT or failure to grow may need higher calorie concentration
Will need prophylactic antibiotics before dental procedures if defect is not repaired


Surgical Repair
Over a period of years the vessels in the lungs will develop thicker walls – the pressure in the lungs will increase and pulmonary vascular disease
If pressure in the lungs becomes too high the un-oxygenated blood with cross over to the left side of the heart and un-oxygenated blood with enter the circulatory system.
If the large VSD is repaired these changes will not occur.


Coarctation of Aorta
COA
7 % of defects
Congenital narrowing of the descending aorta
80% have aortic-valve anomalies
Difference in BP in arms and legs (severe obstruction)+


Diagnosis and Treatment
In 50% the narrowing is not severe enough to cause symptoms in the first days of life.
When the PDA closes a higher resistance develops and heart failure can develop.
Pulses in the groin and leg will be diminished
Echocardiogram will show the defect in the aorta


Treatment
Prostaglandin may given to keep the PDA open to reduce the pressure changes
The most common repair is resection of the narrowed area with re-anastomosis of the two ends
Surgical complications – kidney damage due to clamping off of blood flow during surgery
High blood pressure post surgery – may need to be on antihypertensives
Antibiotic prophylactic need due to possible aortic valve abnormalities.


Pulmonary Stenosis
PS
7% of defects
Obstruction of blood flow from right ventricle
Hypertrophy of right ventricle
If severe cyanosis due to right-to-left shunt


Pulmonary Valvar Stenosis
In pulmonary valvar stenosis the pulmonary valve leads to narrowing and obstruction between the right ventricle and the pulmonary artery.
Thickened tissue become less pliable and increases the obstruction
Right ventricle must work harder to eject blood into the pulmonary artery.


Diagnosis and Treatment
Diagnosis: heart murmur is heard – clicking sound when the thickened valve snaps to an open position.
Electrocardiogram would be normal
Echocardiogram most important non-invasive test to detect and evaluate pulmonary stenosis
Cardiac Catheterization – to measure pressures and measure the stenosis


Treatment
Cardiac Catheterization to dilate the valve and open up the obstruction.
Open- heart procedure would only needed for more complex valve anomaly.


Tetralogy of Fallot (TOF)
6% of defects
Most common cardiac malformation responsible for cyanosis in a child over 1 year


TOF
Four Components
VSD
Pulmonary stenosis – narrowing of pulmonary valve
Overriding of the aorta – aortic valve is enlarged and appears to arise from both the left and right ventricles instead of the left ventricle
Hypertrophy of right ventricle – thickening of the muscular walls because of the right ventricle pumping at high pressure


Clinical Manifestations
Dependent on degree of right ventricular outflow obstruction.
Right-to-left shunt
Clubbing of digits
"tet" spells - treated by flexing knees forward and upward
Severe irritability due to low oxygen levels


Diagnosis
Cyanosis
Oxygen will have little effect on the cyanosis
Loud heart murmur
Echocardiogram – demonstrates the four defects characteristic of tetralogy


Treatment
If oxygen levels are extremely low prostaglandins may be administered IV to keep the PDA open
Complete repair is done when the infant is about 6 months of age
Correction includes
Closure of the VSD with dacron patch
The narrowed pulmonary valve is enlarged
Coronary arteries will be repaired
Hypertrophy of right heart should remodel within a few months when pressure in right side is reduced


Long Term Outcomes
Leaky pulmonary valve that can lead to pulmonary insufficiency
Arrhythmias after surgery
Heart block – occasionally a pacemaker is necessary
Periodic echocardiogram and exercise stress test or Holter evaluation


Aortic Stenosis
6% of defects
Aortic valve: has two rather than three leaflets. Leaflets are thickened or fused.
Obstruction of blood flow from left ventricle
Mild symptoms: dizziness, syncope, angina, fatigue
30% incidence of sudden death


Aortic Stenosis
Causes obstruction to blood flow between the left ventricle and aorta.
Most common form is obstruction of the valve itself
When the aortic valve does not open properly the left ventricle must work harder to eject blood into the aorta.
Left ventricular muscle becomes hypertrophied.


Diagnosis
Heart murmur or AS is a turbulent noise caused by ejection of blood through the obstructed valve.
Electrocardiogram is usually normal
Echocardiogram will show the obstruction and rule out other heart anomalies
Exercise stress test – provides information on impact of the stenosis on heart function


Treatment
Cardiac catheterization – balloon dilation of the narrowed valve.
Surgical valvotomy if the closed procedure does not work – often done when patient is older when severe calcium deposits further obstruct the valve.
Recurrent valve obstruction is a complication and if valve replacement is done too early the child may outgrow the valve.
Antibiotic prophylaxis especially if valve replacement


Hypoplastic Left Heart
One of the most complex defects seen in the newborn and the most challenging of all the congenital defects
All the structures on the left side of the heart are severely underdeveloped.
Mitral and aortic valves are either completely closed or are very small – left ventricle is tiny – aorta is small and often only a few millimeters in diameter


HLH
Life threatening shock develops when the ductus arteriosis closes
Low oxygen saturations – will not increase with oxygen administration
Pulses will be weak in all extremities
Plan to deliver infant in a hospital capable of providing the aggressive treatment needed


Treatment
Three staged procedure to reconfigure the cardiovascular system
Norwood – right ventricle becomes the systemic ventricle pumping blood to the body
Glenn done at 3-6 months
Fontan done at 2 -3 years of age


Long Term Complications
Easily tiring when participating in sports or other exercises
Formation of blood clots – heparin or Coumadin use
Heart arrhythmias – pace maker
Cardiac failure


Bacterial Endocarditis
Infection of endocardial surface of the heart
History of CHD, Kawasaki Disease, Rheumatic Fever, or prosthetic valves are more susceptible to infection
Prophylactic antibiotics with dental care, throat, intestinal, urinary or vaginal infections or surgery.


Kawasaki Disease
Acute-self limiting disease
Generalized vasculitis
Peak incidence 6 months to 2 years
More common in males and Japanese

http://www.aafp.org/afp/990600ap/3093.html


Clinical Manifestations
High fever
Conjunctivitis
Strawberry tongue
Edema of hands and feed
Reddening of palms and soles
Lymph node swelling


Blood Values
Elevated WBC
Elevated ESR
Elevated platelets


Management
Intravenous gamma globulin
High dose of ASA while in hospital
Low dose ASA upon discharge
Base-line echocardiogram to assess coronary artery status