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Respiratory Alter.

Test #2

QuestionAnswer
Otitis Media middle ear infection
Common cause of otitis media eustachian tube - straighter in younger children and does not drain properly
Peak age for otitis media 6 months - 2 yrs
risk factors *winter, household w/ smokers, males, formula fed babies
Most common etiology *hemophilus influenzae *streptococcus pneumoniae *moraxella catarrhalis
Acute otitis media rapid onset & short duration (3wks)
acute otitis media with effusion A.O.M with fluid also present in middle ear
subacute otitis media with effusion middle ear infection & effusion lasting 3wks - 3 months (assoc. with a low grade fever)
chronic otitis media with effusion middle ear infection with effusion persisting beyond 3 months (assoc. with low grade fever and fullness in ear)
Clinical Manifestations O.M. *pulling ears *fever *irritable/dizzy *purulent drainage may or may not be present
Diagnostic evaluation for O.M middle ear effusion w/ 1 or more of the following: erythema of tympanic membrane, bulging TM, absent landmarks, poor light reflex w/ otoscope, limited TM mobility, earache
Therapeutic Management for O.M *wait longer to tx w/ abx *abx 10-14 days for non-draining: PE tubes topical ear drops recommended *analgesics *decongestants *Myringotomy- incision in TM
Candidates for prophylaxis therapy of O.M. *3 episodes of O.M. in a 6 month period *2 episodes before 6 months
Complications of O.M. Hearing Impairment, Chronic effusion
Treating complications of O.M Pressure Equalizer tubes
Complications of PE Tubes Meningitis, Subdural empyema, Mastoiditis
Removal of PE Tubes remian in 6 months before spontaneously rejection
Parent Education for O.M. *no bottle propping *no smoking around child *Compliance
Tonsillitis inflammation & infection of the masses of lymphiod tissue that encircle the pharyngeal cavity. Tonsils filter & protect respiratory and alimentary tracts from invasion by pathogenic organisms
Size of tonsils in child > in adults to protect agains URI when especially susceptible
Palatine or Faucial Tonsils Visualized during oral exam
Pharyngeal tonsils AKA adenoids, posterior wall of NP, opposite posterior nares
Lingual tonsils base of tongue
Tubal Tonsils near posterior NP opening of eustachian tubes
Clinical manifestations of tonsilitis *sore throat, fever, dysphagia, anorexia, vomiting *tonsils enlarged w/ yellow exudate *difficulty swallowing
Therapeutic management for tonsilitis bed rest, antipyretics, cool mist vaporizer, liquid diet, warm saline gargle, throat culture to r/o strep, Pen x 10 days for strep, sx tx is controversial
Tonsilectomy removal of palatine tonsils
What happens to the lingual and tubal tonsils when palatine tonsils are removed? they enlarge to compensate and can pharyngeal and eustachian tube obstruction
What is the most common surgery performed after the newborn period? tonsilectomy
At what age should tonsils be removed? after 3-4 yrs of age d/t blood loss and possible regrowth and hypertrophy of lymphoid tissue
Adenoidectomy is recommended for... recurrent O.M. to prevent hearing loss, hypertrophic adenoids that obstruct breathing, *over the age of 3-4
Post-op assessment of adenoidectomy hearing, smell and taste (expect improvement)
Pre-op assessment of tonsilectomy/ adenoidectomy *bleeding tendencies (site is very vascular) *Baseline vitals *loose teeth (so they arent dislodge and swallowed or aspirated)
Post-op care for tonsil/adenoidectomy *position on abd. or side to facilitate drainage *discourage coughing and clearing of throat *inspect all secretions & emesis for blood *avoid crying, give analgesics, ice collar
S/S of hemorrhage in tonsil/adenoidectomy frequent swallowing, increased pulse
Risk period for hemorrhage in tonsil/adenoidectomy first 24 hrs *7-14 days post-op d/t sloughing
Things to avoid with tonsil/adenoidectomy red/brown fluids, straws (may percipitate bleeding), citrus juice, milk/icecream,
Food and fluids for tonsil/adenoidectomy cool H2O, crushed ice, flavored popsicles, or diluted juice, soft food 1-2 days post-op or as tolerated
Mononucleosis acute self-limiting infectious disease common among young persons up to 25 years of age
Mono cause Epstein Barr Virus or Cytomegalovirus- both are herpes simlex family viruses
Mono incubation and infection *communicable through direct contact with oral secretions *incubation period is 4-6wks
Cardinal sign of mono *general malaise * fever *sore throat *cervical lymphnoid adenopathy
Early warning signs of mono *flu like symptoms *malaise *headache *low grade fever
Associated symptoms of mono *splenomegaly *hepatic involvement *macular eruption (if abx given virus-drug reaction) *exudate *pharyngitis/tonsilitis)
Heterophil Antibody Test used to diagnose mono- determines the extent to which a patients serum will agglutinate sheep RBCs (titer of 1:160 is diagnostic)
Rapid Response tests for mono Monospot slide test- rapid sensitive, inexpensive and easy to perform. *can detect significant agglutination at lower levels which permits earlier diagnosis
Therapeutic management for mono *symptomatic tx (mild analgesics) *bed rest *penicillan of strep + *activity restriction if splenomegaly is present
Prognosis of mono generally good *acute symptoms disappear in 7-10 days *fatigue may subside in 2-4 weeks *mar require restricted activity for 2-3 months
Croup Syndrome etiology usually viral
Croup peak age 3months to 3 years
Croup incidence increased occurrence in the winter months
Croup symptoms *hoarseness *barky/brassy cough *inspiratory stridor * respiratory distress-co2-respiratory acidosis-respiratory failure
Acute Laryngotracheobronchitits (LTB) Most common croup syndrome (AKA viral croup)
Incidence of LTB 3-8 years (usually <5yrs affected)
LTB etiology *para inlfuenza viruses *respiratory syncytial virus (RSV)
LTB progression rapid, edema and inflammation proceeds to vocal chords and lower airway (can go to bed in good condition and wake-up in respiratory stridor)
LTB therapeutic management *high humidity via cool mist tent * oxygen prn *racemic epinephrine (fast acting anti-inflammatory) *corticosteroids *keep infant calm *monitor resp *ET tube or trach set up at bedside *increase fluids
Acute Spasmodic Laryngitis (Spasmodic Croup)Etiology Viral with allergen component
Acute Spasmodic Laryngitis incidence 3 months to 3 years
Spasmodic Croup Progression rapid, usually occurs at night with sudden wakening of symptoms, subsids in a few hours (cold night air sometimes relieves spasms)
Therapeutic management of Spasmodic Croup self-limiting, cool mist tent at night, hospitalized if severe, Racemic Epinephrine/ corticosteriods if severe
Acute Epiglottittis a serious life threatening inflammatory process at the epiglottis. Results in tracheal obstruction
Acute Epiglottittis Etiology Bacterial Croup (commonly hemophilus influenza B)
Peak age for Acute Epiglottittis 2-6 years
Clinical manifestations of Acute Epiglottittis *sudden onset *pale/shocky *respiratory distress *frightened *assumes tripod position *drooling
DO NOT attempt to visualize throat with tongue blade with.... Acute Epiglottittis
Therapeutic Management for acute epiglottittis *notify physician *prepare to assist w/ tracheostomy/ intubation *intubated til swelling subsides (48hrs) *humidified oxygen *IV abx, corticosteriods
Prevention of acute epiglottittis HIB vax *begins at 2 months: administration has greatly decreased incidence
Acute bronchiolitis bronchiole mucosa swells and fills with exudate
Incidence of acute bronchiolitis *fall and winter months * 1st and 2nd year of life (rare after 2yrs)
Etiology of actue bronchiolitis *RSV *Adeno and Para Influenza virus
Clinical Manifestations of acute bronchiolitis *gradual onset of respiratory distress *Barrel chested d/t trapped air & over inflation *usually occurs with URI expect nasal discharge and mild fever
Diagnostic eval. for acute bronchiolitis RSV made by ELISA from N.P secretions *must r/o asthma/RAD *high occurence in cystic fibrosis patients
Therapeytic management for acute bronchiolitis *mist tent to loosen secretions *Bronchodialator/steroids *Ribavirin by hood, tent or mask for 12 hours *wear hepta filter mask-toxic to pregnant women
RSV protocol *coherent clients/nurses *contact/droplet isolation *handwashing *avoid succeptible patients
Prophylactic therapy for RSV Respigam vax (Gamma Globulin) decreases severity of infection but does not prevent it
Cystic Fibrosis a generalized multisystem disorder affecting the exocrine glands. Defect in CFtransmembrane Regulator (CFTR) proteins found in lungs, GI, sweat glands and GU *the substance they secrete are abnormally viscous
Cystic Fibrosis etiology Autosomal recessive trait, males > females
Cystic Fibrosis patho secretions of the exocrine glands are thick and sticky rather than thin and slippery
Pulmonary effects of cystic fibrosis decreased cilliary action & mucous secreting cells have increased production of thick secretions
Bronchioles and bronchi effects of cystic fibrosis become plugged- results in irreversible fibrotic changes of the lungs
Clinical manifestations of cystic fibrosis *pulmonary infections *emphysema *atelactasis *pneumothorax *nasal polyps *chronic sinusitis *hemoptysis *cough *wheezing *increased ap chest diameter *decreased exertional endurance
Hepatic signs of cystic fibrosis intrahepatic biliary tract becomes obstructed and causes biliary cirrhosis (result in portal HTN)
Reproductive signs of cystic fibrosis *fibrosis of epididymis and vasdeferans *obstruction of fallopian tubes *causes infertility
GI and pancreatic signs of CF become obstructed, enzymes do not reach intestines and digestion is impaired-results in loss of foodstuff in stools
Earliest signs of CF affecting GI and pancreas *rectal polyps(3mo-3yr)*intussusception<2yrs *heat prostration *pancreatic fibrosis *glucose intolerance *diabetes *pancreatitis *FTT w/good appetite *frequent smelly stools *pot belly *vomiting *Maldigestion *hyperglycemia
Cardiac signs of CF Cor pulmonale (hypertrophy of right ventricle) *clubbing of fingers in older children
Metabolic signs of CF Have increased permeability to chloride *salty saliva *hypoelectrolytemia *metabolic acidosis *growth retardation
CF diagnostic evaluation *usually done before 6mo *health/family history *sodium levels *meas. trypsin *enzymes in stool *chest X-ray
Immunoreactive Trypsinogen Test shows increased blood levels of IRT an enzyme produced by the pancreas in the newborn (CF testing)
BMC (Borehringer-Mannheim Corp) meconium strip test includes lactose and protein content: present in babies with CF & used for screening
Pulmonary function studies for CF decreases vital capacity/flow rates & increases residual volume or increased total lung capacity or both (after 4yrs)
Definitive diagnosis for CF postive sweat test and one or more criteria (fam hx., absent enzymes, lung changes, steatorrhea)
Goal of care in CF prevent and control pulmonary infection
Preventing and controlling pulmonary infection in CF *bronchodilators *mucolytics *antihistamines *chest physiotherapy & postural drainage *breathing exercises * bronchopulmonary lavage
Lobectomy in CF remove portion of lung *symptomatic treatment that retards progression of pulmonary involvement
Lung transplant in CF *living donors: one lobe from 2 donors *cadaveric donor: transplanted from brain dead donor -50% are alive in 5 years
Up and coming treatment for CF Denufusol- in phase 3 testing. Given fast track status with FDA. Enhances lung hydration and mucociliary mechanisms
Apnea of infancy cessatation of breathing for 20 seconds or more associated with bradycardia, cyanosis or pallor
Incidenc of infant apnea *2wks-6mo *while asleep
Etiology of infant apnea *seizure disorder *GER *significant anemia *sepsis *hypoglycemia *impaired regulation of breathing *maternal cocaine abuse
Therapeutic management of infant apnea *cardiopulmonary monitoring *treat underlying cause *theophylline to decreases apnea swells
Interventions for infant apnea *start with gentle stimulation *turn supine *rub or pat trunk *flick the feet *never shake *proceed with cpr if no brething in response to the above
SIDs sudden death, unexplained by history, which through postmortem exam fails to demonstrate an adequate cause of death
SIDs etiology unkown
Theories of SIDs *brainstem abnormalities *sleep habits *CO2 breathing *smoking
Created by: jas067
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