respiratory-final Flashcards

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1
Q

s/s pnuemonia

A

Cough Fever Wheezing Dyspnea Poor Feeding Lethargy Vomiting Abdominal pain

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2
Q

clinical findings of Pneumonia

A

ENT: May be normal or nasal congestion, OM, pharyngitis may be present Lungs: Rales, diminished breath sounds, rhonchi. Respiratory distress Heart: Tachycardia Abdomen: Right sided pain/tenderness General: Poor perfusion, lethargy; ill appearing

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3
Q

who should get a chest xray if pnuemonia is suspected?

A

Healthy, immunized children who will be treated as an outpatient do not require CXR Particularly helpful when the dx is uncertain Hospitalized children and children with respiratory distress should have a CXR

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4
Q

are blood cultures necessary with pneumonia?

A

not necessary for patients treated on an outpatient basis Indicated for hospitalized patients as well as for patients who deteriorate or do not improved

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5
Q

additional testing for pneumonia is

A

CBC CMP Influenza RSV Strep

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6
Q

Indications for hospitalization with pneumonia

A

Infants Apnea/Grunting/respiratory distress Respiratory rate >70 Poor feeding Comorbidities SaO2 <92% Older Children Grunting/respiratory distress Respiratory rate >50 SaO2 <92% Unable to tolerate po fluids Comorbidities

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7
Q

Outpatient Antimicrobial Therapy for pneumonia

A

Outpatient Antimicrobial Therapy 60 days to 5 years: Amoxillin 90mg/kg/day; divided bid If penicillin allergic: Zithromax (10mg/kg x1 day then 5mg/kg/day x5d Biaxin (15mg/kg/day; divided bid) Cefzil (30mg/kg/day; divided bid) School aged children & adolescents Amoxillin Consider macrolide if mycoplasma is suspected Zithromax Biaxin

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8
Q

Asthma: clinical manifestations

A

Chronic Inflammation Bronchial hyper-responsiveness after exposure to allergens, viruses, cold air, exercise, irritants leads to Wheezing Bronchospasm Dyspnea Cough

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9
Q

Asthma Risk Factors

A

Asthma Risk Factors Frequent Colds Frequent OM Food Allergies Atopic Dermatitis (Eczema) Allergic Rhinitis Persistent Wheezing after age 3

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10
Q

The Road to Asthma

A

The Road to Asthma Food Allergies Allergy to milk proteins IgE antibody response Markers for atopy Dermatitis 3mo – 3 years Follows exposure to food or external allergen

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11
Q

Diagnostic Criteria

A

Diagnostic Criteria Periodic symptoms of airway obstruction Airflow obstruction symptoms that can be at least somewhat reversed Exclusion of alternate diagnosis

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12
Q

symptoms of asthma

A

Asthma Symptoms Cough Wheeze Cough with exercise and/or nocturnal Dyspnea Sensation of chest tightness Sputum Asthma Pattern of Symptoms Continuous or Intermittent Day or Night Time Seasonal, Perennial or Both Onset and Duration

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13
Q

Asthma Precipitating Factors

A

Asthma Precipitating Factors Allergens (outdoors & indoors) Irritants Viruses Drugs Stress Foods Seasonal changes Other GERD, Sinusitis, rhinitis, menses

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14
Q

Asthma Diagnosis

A

Asthma Diagnosis Difficult to diagnose if child <3 History Family History Social History Physical PFT

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15
Q

asthma Prevention

A

Prevention Primary Prevention Breast feeding Hold solid foods until 4 months Healthy diet Exposure to smoke Minimize home allergens Abx sparingly Prevention Secondary Prevention Flu Vaccine Immunotherapy Avoid Triggers Pharmacology ICS, LTRA, Oral Steroids Prevention Tertiary Prevention Daily meds Pre-exercise prophylaxis Management of acute exacerbations

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16
Q

asthma Classification & Treatment

A

Classification & Treatment Mild Intermittent Day: 2 times or less per week Night: 2 nights or less per month PEF/FEV 80% of expected No daily meds needed SABA PRN Mild Persistent Day: >2/week, less than 1/day Night: 2 or more/month PEF/FEV 80% of expected Low dose ICS SABA PRN Moderate Persistent Day: Daily Night: More than 1/week PEV/FEV 60-80% of expected Low dose ICS (,<5), Med >5) LABA Severe Persistent Day: Continual Night: Frequent PEF/FEV: 60% or less than expected High dose ICS LABA

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17
Q

cf

A

Cystic Fibrosis Exocrine gland dysfunction Chronic respiratory infections Pancreatic enzyme deficiency 90% of patients have lung involvement Principle cause of death is respiratory failure

18
Q

cf

A

Resultant reduced height of epithelial lining fluid and decreased hydration of mucus results in mucus that is stickier to bacteria, which results in infection and inflammation. These abnormalities result in viscid secretions in the respiratory tract, pancreas, GI tract, sweat glands, and other exocrine tissues. Increased viscosity of these secretions makes them difficult to clear. defects result in decreased chloride excretion, increased sodium and water reabsorption across endothelial cells

19
Q

Cystic Fibrosis
History intestinal symptoms? respiratory? pancreatic? gu symptoms

A

Intestinal Symptoms Infants Intestinal obstruction at birth Meconium Ileus, Volvulus, Intestinal Atresia Delayed Meconium passage; prolonged jaundice Infants and Children Frequent Stooling; oil/fat in stools FTT Intussusception Rectal prolapse Pancreatic Symptoms Pancreatic Insufficiency Fat soluable vitamin deficiency Malabsorption of protein, carbs and fats Steatorrhea (frequent, poorly formed, large, bulky, foul-smelling, greasy stools that float in water) FTT, flatulence, abd pain, abd distention, anorexia, GER Respiratory Symptoms Chronic or recurrent cough; dry and hacking at the beginning and can produce mucoid (early) and purulent (later) sputum. Prolonged symptoms of bronchiolitis occur in infants. Coughing fits that can lead to vomiting Recurrent wheezing, recurrent pneumonia, atypical asthma, pneumothorax, hemoptysis, and digital clubbing (may be the initial manifestation) Dyspnea on exertion, history of chest pain, recurrent sinusitis, nasal polyps, and hemoptysis may occur GU Symptoms Males Vas deferens absence causes males sterility. Hyrdoceles Undescended Females Fertility is maintained, but may be decreased. Secondary sexual development is often delayed. Amenorrhea may occur in patients if the patient has severe nutritional or pulmonary involvement.

20
Q

Cystic Fibrosis
Physical

A

Cystic Fibrosis
Physical Pulmonary Tachypnea Respiratory distress Wheeze and/or rales Cough (dry or productive of mucoid or purulent sputum) Increased anteroposterior diameter of chest Clubbing Cyanosis Hyperresonant chest upon percussion Cystic Fibrosis
 GI Abdominal distention Hepatosplenomegaly (fatty liver and portal hypertension) Rectal prolapse Dry skin (vitamin A deficiency) Other Findings Scoliosis Kyphosis Swelling of submandibular gland or parotid gland Rhinitis Nasal Polyps

21
Q

Work Up for cf

A

Work Up Sweat Test quantitative pilocarpine iontophoresis test (QPIT) to collect sweat and perform a chemical analysis of its chloride content is currently considered to be the only adequately sensitive and specific type of sweat test Neonatal Screening: Multiple states in the US have implemented neonatal screening for cystic fibrosis. All screening algorithms in current use in the United States rely on testing for immunoreactive trypsinogen (IRT) as the primary screen for cystic fibrosis.7 The presence of high levels of IRT, a pancreatic protein typically elevated in infants with cystic fibrosis, warrants second level testing in the form of repeat IRT testing, DNA testing, or both. Within these 2 categories, various modifications are used.

22
Q

findings on cxr for cf

A

CXR Hyperinflation peribronchial thickening

23
Q

Cystic Fibrosis
Treatment

A

Cystic Fibrosis
Treatment Multidisciplinary Approach Medical Home PCP, Pulmonology; Gastroenterology, Nutritionist, ENT, Cardiology, Surgery Diet: High energy, high fat Exercise Bronchodilators, pulmonary hygiene Pancreatic Enzyme Replacement

24
Q

ages for Croup

A

Croup Common viral respiratory illness Kids 6-36 months, but can occur in older children as well, especially up to age 5 More common in the fall and winter Pathogens Viruses Parainfluenza virus accounts for approximately 80% of cases Adenovirus RSV Enterovirus

25
Q

Pathogens croup

A

Pathogens Viruses Parainfluenza virus accounts for approximately 80% of cases Adenovirus RSV Enterovirus

26
Q

podromal symptoms and s/s of croup

A

Croup is often preceded by mild URI symptoms Sore throat, low grade fever, rhinorrhea Stridor and respiratory distress generally develop suddenly and generally late in the evening Symptoms include: Barky cough Stridor Respiratory distress

27
Q

What is used to test child for croup?

A

Westley Score 0-3 = Mild Occasional barking cough, no stridor at rest, and mild or absent suprasternal or subcostal retractions. 3-6= Moderate frequent cough, audible stridor at rest, and visible retractions, but little distress or agitation. >6 = Severe frequent cough, prominent inspiratory (and, occasionally, expiratory) stridor, conspicuous retractions, decreased air entry on auscultation, and significant distress and agitation. Lethargy, cyanosis, and decreasing retractions are harbingers of impending respiratory failure.

28
Q

Croup Clinical Diagnosis

A

Croup Clinical Diagnosis Soft – Tissue neck films Strep Testing Influenza Laryngoscopy

29
Q

Croup Treatment

A

Croup Treatment Decadron .6mg/kg IM .15-.3mg/kg have been shown to be effective Racemic Epinephrine 3 hour observation Humidified oxygen or misty air Little empircial evidence of efficacy

30
Q

what is Bronchiolitis

A

Bronchiolitis is a virally induced acute inflammation of the lower respiratory tract in children <2 years old Inflammation increased mucous production, airway edema and necrosis of epithelial cells Clinically children may have rhinitis, cough, tachypnea, wheeze, rales, accessory muscle use, and/or nasal flaring

31
Q

what age does bronchiolitis usually occur

A

< 2

32
Q

bronchiolitis Clinically

A

Clinically children may have rhinitis, cough, tachypnea, wheeze, rales, accessory muscle use, and/or nasal flaring

33
Q

how long does bronchiolitis last

A

bronchiolitis is a self limited disease, with a median duration of 12 days Bronchiolitis is the top cause of hospitalization for children less than 1 year old

34
Q

Diagnose of Bronchiolitis

A

Diagnose Bronchiolitis by History and Physical (B; Strong Recommendation) Assess risk factors for severe disease (B; Moderate Recommendation) Age < 12 weeks Premature gestation Cardiopulmonary disease Immunodeficiency Radiographic or Laboratory studies should not be obtained routinely (B; Moderate Recommendation) Virological testing should not change management

35
Q

So when should you consider obtaining a CXR?

A

So when should you consider obtaining a CXR? Severe respiratory distress/ potential ICU admission Child has signs/symptoms of airway complication such as pneumothorax Child with suspected bronchiolitis is not following anticipated clinical course Unclear diagnosis

36
Q

meds for bronchiolitis

A

2006: “A carefully monitored trial of an a -adrenergic or B–adrenergic medication is an option. Inhaled bronchodilators should be continued only if there is a documented positive clinical response to the trial using an objective means of evaluation”

37
Q

albuterol for bronchiolitis?

A

2014: “Clinicians should not administer albuterol to infants and children with a diagnosis of bronchiolitis (B; Strong Recommendation)

38
Q

epi and bronchiolitis?

A

“Clinicians should not administer epinephrine to infants and children with a diagnosis of bronchiolitis” (B; Strong Recommendation)

39
Q

So when should you consider using epinephrine for bronchiolitls?

A

So when should you consider using epinephrine? “potentially as a rescue agent in severe disease” Be weary of using in ER to prevent hospital admission Short action of medication No overall reduction in rate of hospitalization by day 7

40
Q

nebulized hypertonic saline and bronchiolitls?

A

2006: No recommendation provided. 2014: “Nebulized hypertonic saline should not be administered to infants with a diagnosis of bronchiolitis in the ED” (B; Moderate Recommendation) 2014: “Clinicians may administer nebulized hypertonic saline to infants and children hospitalized for bronchiolitis” (B; Weak Recommendation)