Ped\'s Exam #3 Study Guide PDF

Title Ped\'s Exam #3 Study Guide
Author Nita Gopinath
Course Pediatric care
Institution Ameritech College of Healthcare
Pages 18
File Size 973.2 KB
File Type PDF
Total Downloads 110
Total Views 131

Summary

Peds exam 3 study guide...


Description

Peds Exam 3 Chapter 27 

Polydactyly: additional 1 or + fingers or toes



Syndactyly: 2 fingers or toes are fused



Pectus Excavatum: funnel chest: indentation in the lower portion of the sternum



Torticollis: sternocleidomastoid muscle is injured and bleeds during birth o Treatment is successful if the child loos in direction of affected muscle



Talipes Disorder: club foot; require a series of casts or braces to gradually correct o If you try to straighten newborn’s feet to midline, if you can straighten then it is NOT a true talipes disorder and won’t require casting.



Developmental Dysplasia of the Hip (DDH): improper formation of the hip socket o Assess:  Newborn:  Barlow sign: feeling of the femur head slipping out of the socket posterolaterally; start w/ knees apart, rotate midline and feel the femur head slip out of the acetabulum









Ortolani sign: clicking or clunking sound when a displaced femoral head reenters the acetabulum; start w/ knees together, rotate laterally and hear femoral head slip into acetabulum Older children who can walk:  Trandelenburg Sign: stand on one leg (the affected leg), the test is positive if the pelvis drops on the side opposite of the leg they are standing on.

Treatment:  Pavlik harness: hold the hips flexed, abducted and externally rotated o Must be worn continuously 23*/day. Except for bathing  Monitor skin integrity

Ankyloglossia: tongue tied; assess for difficulty w/ feeding



Pierre Robin Sequence Syndrome: triad of micrognathia; small mandible, cleft palate & glossoptosis (tongue is malpositioned downward) o Causes severe upper airway obstructionrespiratory distress  Keep side-lying or prone not supine for sleeping (until they can roll over) to avoid obstruction



Esophageal Atresia: (EA) the lumen of the esophagus doesn’t form completely; results in a “blind pouch” that doesn’t connect to anything = no access to GI



Tracheoesophageal Fistula: opening develops between the closed lower esophagus and trachea

o

Assessment:









Mom may have had polyhydramnios (too much amniotic fluid) do a VACTERL work up  Lots of mucus, “blowing bubbles & frothy sputum”, drooling, periodic cyanotic episodes, & drooling. Have suction available because they can’t handle their secretions Meconium plug syndrome: bowel obstruction from meconium; associated w/ Hirschsprung disease, cystic fibrosis, hypothyroidism o Tx: saline enema

Hydrocephalus: accumulation of an excess amount of CSF in brain o Assessment:  Measure head circumference at birth to make comparisons  Sunset eyes = sclera shows above the iris because of upper lid retraction  Assess fontanelles for width and tension o Tx:  If caused by over production of fluid, then diuretic is given  If more extensive, a VP (ventriculoperitoneal) Shunt (drain excess fluid from ventricles into peritoneum Neural Tube Disorders: not all neural tube disorders involve the spinal cord

o o o

Spina bifida: collective term for all spinal cord disorders Spina bifida occulta: benign disorder; posterior side of vertebrae fail to fuse; dimpling of skin or tuft of hair is a sign Meningocele: the meninges (pia, arachnoid & dura maters) herniate through unformed vertebrae = protruding circular mass



o

Tx: immediate surgery to replace the meninges and close the gap in the skin to prevent infections Meningomyelocele: common birth defect affecting the CNS; the meninges and the spinal cord protrude through the vertebrae; spinal cord ends at protrusion; causes partial or complete paralysis  Associated w/ hydrocephalous  Protect the sac  Requires surgery to close the gap

Chapter 40: Ped’s Respiratory Disorders     







Cough: reflex; nerves in respiratory tract stimulated by dust, chemical, mucus or inflammation Paroxysmal Coughing: series of expiratory coughs after a deep inspiration; common w/ pertussis (whooping cough) or aspiration Tachypnea: increased RR; 1st indication of airway obstruction in children o depth and quality of respiration are also important Anoxia: cells in the body lack O2 Hypoxia: decreased oxygen in body cells  children/infants become anxious and restless o Cyanosis: blue tinge to the skin; indication of hypoxia  Degree of cyanosis is not an accurate indicator of the degree of hypoxia Hypoxemia: lack of O2 in the blood o s/s: tachypnea, decreased alertness & activity, inability to feed because can’t suck and breathe at the same time retractions: more forceful inspiration than normal; required to inflate lungs d/t airway obstruction, stiff noncompliant lungs, intrapleural pressure is decreased to the point that the intercostal spaces draw inward

Adventitious Sounds: o Vibrations: air being forced past and obstruction like mucus o Rhonchi: snoring o Stridor: harsher, strident sound on INSPIRATION; base of tongue or in larynx o Wheezing: EXPIRATORY whistle; heard when obstruction is in the lower trachea or bronchioles o Crackles/rales: snapping sound of alveoli popping open; heard when alveoli become fluid filled

    











o Will have diminished breath sound when alveoli are so filled that air can’t enter them Hyperinflation: inability to exhale completely; air is chronically trapped in alveoli; aka pigeon breast Spirometry: most common test of lung function in children o Measures the peak expiratory flow amount of air that can be forced out of the lungs Pharyngitis: infection and inflammation of the throat o Caused by an ADENOVIRUS Streptococcal pharyngitis: can lead to acute rheumatic fever & glomerulonephritis if not treated Epistaxis: nosebleed; very common in children o Keep children in upright position with head tilted slightly forward, not back into the nasopharynx o Hold pressure to the cartilage on the sides of the nose with your fingers for 10 minutes Congenital laryngomalacia/tracheomalacia: weak laryngeal structure that collapses more than usual on inspiration o Stridor: high pitch crowing sound on INSPIRATION  Caused by a blocked airway Croup: laryngotracheobronchitis; inflammation of the larynx, trachea, & major bronchi. o caused by para-influenza virus o assessment:  barky cough (like a seal), dyspnea, inspiratory stridor, retractions o tx:  cool moist air & corticosteroid (dexamethasone) or Racemic Epinephrine via nebulizer to reduce inflammation bronchiolitis: inflammation of fine bronchioles & small bronchi o common in children < 2 years of age o main cause is RSV- Respiratory Synapsical Virus  RSV: droplet lives 6* on surfaces  Hand hygiene prevents the spread  Droplet precautions  Keep RSV pts together to prevent spread asthma: chronic inflammatory disorder of the airways  obstruction of the bronchioles o assessment:  get thorough hx  wheezing {audible on expiration}; dyspnea, cough  pulmonary function tests (studies): most accurate tests for diagnosing asthma and its severity o tx/management:  bronchodilators: inhalers; beta2 agonists (albuterol, terbutaline)  cholinergic antagonists: blocks parasympathetic nervous systemrelief of acute bronchospasms  anti-inflammatory agents: decrease airway inflammation (prednisone, solumedrol)  combined meds: steroid w/ long acting beta2 agonist atelectasis: alveoli collapse

 



o management: keep child in semi-fowlers position for the best lung expansion tuberculosis: (TB) must have sputum culture to positively confirm a diagnosis of active TB Cystic fibrosis: respiratory disorder; mucus glands secrete and excess of mucus, and it is thicker than normal; causes obstruction of lungs, pancreas, liver, small intestine & reproductive system o Pancreas involvement: digestive enzymes necessary for the digestion of fat become so thick they plug the ducts; eventually mucus cells atrophy and stop producing enzymes. Stools become large, bulky, & greasy (steatorrhea) o Assessment:  Sweat testing: collect sweat from 2 different sites  Confirmation of CF o Therapeutic Management:  Medications  Digestion: o Pancrelipase: enzyme replacement to help w/ digestion of fats  Administer capsules w/ all meals & snacks; can open capsules and sprinkle on food  Respiratory: o Proventil/albuterol: short acting beta2 agonist o Atrovent: cholinergic antagonist (anticholinergic) o Dornase alfa: (pulmozyme) decreases the viscosity of mucus & improves lung function  Assess sputum thickness & pt ability to expectorate  Antibiotics: specific for pulmonary infection o Tobramycin o Ticarcillin o Gentamicin  Vitamins o Daily multivitamin o Fat soluble vitamins Therapeutic techniques for Respiratory Disorders: o Chest physiotherapy: CPT;  Change position  Percussion: striking a supped or curved palm against the chest to determine the consistency of tissue beneath surface area  Vibration: as child exhales vibrate hand against child’s chest; mechanically loosens secretions o Nebulizers: mechanical devices that provide a stream of moistened air directly into the respiratory tract o Pharmacologic Therapy:  Nasal sprays: moisten & loosen nasal secretions  Antihistamines: reduce mucus production in presence of allergies  Corticosteroids: reduce airway inflammation; brief use of nasal decongestants may be advised  Bronchodilators: open lower airway



 Antibiotics: may be ordered if the illness is caused by a bacterial infection Improving oxygenation: o Tracheotomy: procedure to create an airway  Tracheostomy: opening in the trachea to create an artificial airway  Primary nursing responsibility when a child with trach tube eats- prevent aspiration of food or fluids into the tube o Incentive spirometer: peds use 4 times daily; to do it right, use on INSPIRATION

Chapter 41: Cardiac Disorders   

Congenital heart disease: anatomic defects born with o Risk factors: maternal: infection, ETOH/drugs, DM Acquired Heart Disease: disorders that develop after birth o risk factors: rheumatic fever, hypertension & hyperlipidemia Fetal Circulation: 

Placenta oxygenates & removes carbon dioxide from the blood  3 Fetal Shunts o Patent Foramen Ovale: flapped opening between atria. Oxygenated blood bypasses the lungs and continues to left ventricle and aorta o Patent Ductus Arteriosus: connects pulmonary artery to the aorta; oxygenated blood bypasses lungs o Ductus Venosus: shunt that allows oxygenated blood in umbilical vein to bypass liver. Blood then enters IVC & enters right atrium



General Assessment of Heart Disorders o Appearance: o Check for cyanosis in mucous membranes of the mouth  If cyanosis increases w/ crying, cardiac dysfunction is suggested. Indicates infant can’t meet the increased circulatory demands of exertion o Ruddy complexion: body has overproduced RBCs (polycythemia)

o

Murmurs: whooshing sound o Innocent heart murmur: sound heard is not concerning o Organic heart murmur: sound heard is a result of heart disease or congenital disorder

Diagnostic tests: o Transthoracic Echocardiography: noninvasive US of the heart gives detailed information of heart structure and function  Primary diagnostic test for congenital heart disease o Cardiac catheterization: invasive test; catheter pass through large vein/artery into the heart.  Diagnose or repair defects  Evaluate dysrhythmias  Access for catheterization is frequently obtained in the femoral vein OR artery but radial or neck access can be used o Post procedure: assess insertion site for bleeding or hematoma  Prevent bleeding by maintaining the affected extremity in a straight position for 4-8 hours Congestive Heart Failure: inability of the heart to supply the oxygenated blood demanded by the body o Clinical Manifestations: o Cool extremities o Peripheral edema o Nasal flaring  Position in Semi-fowlers ↑Pulmonary Blood Flow Disorders o Patent Ductus Arteriosus: (PDA) ductus arteriosus (between pulmonary artery & aorta) doesn’t close ↑ pulmonary blood flow o Assessment:  Wide Pulse Pressure (90/40)  Bounding pulses o







Atrial Septal Defect: hole in septum between R & L atria↑ pulmonary blood flow o Assessment:  Loud, harsh murmur w/ fixed split 2nd heart sound

o



Ventricular Septal Defect: MOST COMMON DEFECT IN CHILDREN

↓Pulmonary Blood Flow Disorders o Tetralogy of Fallot:  4 Components:  Pulmonary artery stenosis o Degree of cyanosis is directly proportional to the degree of pulmonary stenosis  VSD  Overriding Aorta  Right Ventricular hypertrophy

 

Assessment:  Hypercyanotic spell or “tet spell”: Episodes of acute cyanosis & hypoxia Management:



Teach Parents: When child becomes cyanotic & dyspneic, place child in a knee-chest position to increase systemic vascular resistance & reduce R to L shunting



Obstruction of Blood Flow o Coarctation of the Aorta: narrowing of the lumen of the aorta  Assessment:  ↑ BP & pulses in Upper Extremities  ↓BP & weak or absent femoral pulse o Absence of palpable femoral pulses from the decrease BP to lower body may be the only symptom



Acquired Heart Disease: o Kawasaki Disease: febrile, multisystem disorder that occurs in children before puberty.  Vasculitis: inflammation of blood vessels; main and life-threatening symptom because it can lead to formation of aneurysms & MI  Strawberry tongue w/ white coating  Enlarged lymph nodes  Observe for symptoms of bowel obstruction; enlarged lymph nodes in abdomen can compress intestines



o

Tx:

 Gamma globulin (IVIG)  ****Aspirin: high dose 80-100 mg/kg/day divided q 6* Rheumatic Fever: inflammatory diseased caused by untreated strep throat infection  Subcutaneous nodules over bony prominence, large joints  Erythema marginatum: rash that appears and disappears rapidly  Tx: antibiotics ranging from 5 years to indefinitely  Encourage periods of rest to ↓ cardiac workload  Can use ASA for tx

Cardiomyopathy: most common cause of heart transplant in children > 1 y.o.  Dilated: most common  Hypertrophic: hypertrophy of Left Ventricle  Most common cause of sudden cardiac death in an otherwise healthy child  Arrhythmogenic Right Ventricular: rare & inherited dz. Causes ventricular tachyarrhythmias & sudden death in young people & athletes o Hypertension: adolescents w/ HTN are advised to not use oral contraceptives (they elevate BP)  Criteria to define childhood HTN: systolic reading above the 95th percentile for the child’s age Cardiac Surgery: chief cure for congenital heart disease o Hypothermia: used to ↓ body temp to reduce metabolic need & slow the HR o Postoperative Care:  Prevent pooling of lung secretions: suction PRN; especially if using ventilator o



Chapter 42: Ped’s w/ Immune Disorders









Immune Response: body’s action plan devised to combat invading organisms o Antigen: foreign substance o Immunity: body’s ability to destroy antigens o Allergen: specific type of antigen that causes and IgE (allergic) antibody response o Humoral Immunity: use B lymphocytes (memory cells) cells that secrete large quantities of immunoglobulins (antibodies {think air force}); fight specific antigens the body has been exposed to before  IgM: Massive response- 1st on scene w/ antibodies specific to antigen  IgG: body recoGnizes a previously seen antigen; IgG’s are immediately produced  Infants have maternal IgG protection for 6 months  Complement activation: cascade response by different proteins that when activated by an antigen cause increased vascular permeability, smooth muscle contraction, chemotaxis (chemical signal calling leukocytes to the area), phagocytosis, & lysis (killing) of foreign antigen  Deficiency in humoral immunity = ↓ antibodies o Cell-Mediated Immunity: hand to hand combat by T lymphocytes; 70-80% of lymphocytes; causes transplant rejection  Developed in bone marrow, but matured (trained) in thymus gland  Cytotoxic  Helper T-cells  Suppressor T-cells HIV/AIDS: virus causes disfunction in immune system by attacking specific T-cells (CD4); symptoms of AIDS in children most commonly begin as frequent respiratory infections o 3 classifications of HIV in children o Tx: Zidovudine: during pregnancy goal is to keep CD4 cell count at >500 cells/mm3  Action: stops replication of the virus; ↓ risk of maternal-fetal transmission  Nursing Considerations:  Administer IV over 60 minutes  Administer around the clock for maximum effectiveness  Monitor labs  Encourage small frequent meals to help w/ loss of appetite & taste  Rx can cause paresthesia’s; teach pt and parents about safety  Only reduces risk of transmission placentally; must remain vigilant w/ hygiene & infection control measures Hypersensitivity: o Type I- Anaphylaxis: IgE; caused by exposure to insect bites, Rx, latex, and foods;  Food allergy: most common cause of anaphylaxis o Type II- Cytotoxic Response: Blood transfusion reaction; only foreign cells are destroyed o Type III- Immune Complex: Autoimmune o Type IV- Cell-Mediated Hypersensitivity or Delayed Hypersensitivity: lymphocytes react to antigens; macrophages called to area; inflammatory response occurs that destroys foreign tissue; ex: PPD TB test; transplant reaction, contact dermatitis Reactions to Allergens o Urticaria: swelling & itching; often from ingested antigens

 



o

Contact dermatitis: rash: related to antigen that touches the skin  Example of a delayed (Type IV) hypersensitivity response

o o

Wheal: small raised bump; looks like mosquito bite Flare: redness that surrounds a wheal  Wheal & flare will appear at site of allergy test from the release of histamine by mast cells

Tolerance: sustained unresponsiveness; when contact w/ allergen can’t be avoided immunotherapy (hyposensitization) is used to produce tolerance Anaphylaxis: TRUE EMERGENCY so fast interventions are necessary o Immediate therapy: IM EPI injection or oral antihistamine o Long-term therapy: corticosteroids; cyclosporine (immunosuppressant) & monoclonal antibody usually used in older adolescents/adults Allergic Rhinitis: risk factor for developing asthma  Perennial Allergic Rhinitis: allergen present year-round; house dust mites, pet hair o assessment:  pale nasal mucous membrane & blackened area under eyes (allergic shiners)

o

Therapeutic Management:

 





Avoid ALLERGENS!!!! Rx:  Antihistamines: educate about rebound effect (after 3 days of use when stop using, will have increased congestion) o Topical steroid used to reduce itching; use sparingly in young infants-thing layer  Immunotherapy  develop tolerance Lichenification: thick, leathery skin; occurs from constant rubbing/itching

Elimination Diet: used w/ food allergies; if uncertain what allergy is, or suspect allergy, start removing most common allergens from diet (peanut (85% of fatalities from food anaphylaxis), milk, wheat, egg, soy, seafood, tree nuts) o Keep a food diary  Colic/fussy eaters could be sign of food allergy

Chapter 43: Infectious Disease in Children 





Stages of infectious disease o Incubation: time between invasion and onset of symptoms; microorganisms grow & multiply in host o Prodromal: time between the beginning of nonspecific symptoms and the onset of disease specific symptoms o Illness: specific symptoms occur o Convalescent: time betwe...


Similar Free PDFs