RESPIRATORY Chap 373-419 Flashcards

1
Q

T/F
FEV1:VC is NORMAL in Restrictive disease

A

TRUE

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2
Q

T/F
FEV1:VC is NORMAL in Obstructive disease

A

False, decreased

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3
Q

At rest, Tidal Volume is _____ml/kg body weight

A

6-7ml/kg

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4
Q

Decreased FEFmax (Maximal Forced Expiratory Flow)
Decreased FVC
Decreased FEV1/FVC

A

Obstructive pulmonary disease (eg. Asthma, cystic fibrosis)

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5
Q

Normal FEFmax (Maximal Forced Expiratory Flow)
Decreased FVC
Normal FEV1/FVC

A

Restrictive pulmonary disease (eg. pneumonia, kyphoscoliosis)

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6
Q

Sudden, unexpected death of an infant taht is unexplained even by autopsy

A

Sudden Infant Death Syndrome (SIDS)

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7
Q

MC congenital anomaly of the nose

Usually associated with syndromes if bilateral
May remain asymptomatic if unilateral until a respiratory tract infection that may cause obstruction

Dx by inability to pass a catheter through each nostril

A

Choanal atresia

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8
Q

Syndrome that is more sommonly associated with choanal atresia

A

CHARGE (Coloboma, Heart disease, Atresia choanae, Retarded growth & development, Genital anomaly, Ear anomalies)

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9
Q

Treatment of choice for choanal atresia

A

Transnasal repair

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10
Q

Drug used to help prevent development of granulation tissue and stenosis post choanal atresia repair

A

Mitomycin C (chemo drug used for gi cancers)

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11
Q

MC type of congenital midline nasal mass

A

Nasal dermoid

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12
Q

MC site of nasal bleeding

A

Kiesselbach plexus

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13
Q

Profuse unilateral epistaxis associated with a masal mass in an adolescent boy

A

Juvenile nasopharyngeal angiofibroma

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14
Q

MC site of nasal polyp

A

Ethmoidal sinus, middle meatus

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15
Q

Unilateral, foul smelling nasal secretion

A

Foreign body

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16
Q

MC complication of common cold (rhinosinusitis)

A

Acute Otitis Media

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17
Q

Sinuses present at birth

A

Maxillary (pneumatized at 4yrs)
Ethmoid (pneumatized at birth)

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18
Q

Patient has persistent, non improving nasal congestion for more than 10 days, with high grade fever (39C), associated with headache and facial pain

Pe: sinus tenderness, with erythema and swelling of the nasal mucosa, purulent discharge, negative transillumination

A

Sinusitis

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19
Q

Initial treatment for acute bacterial sinusitis

A

Amoxicillin (45mkday BID)

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20
Q

Treatment for sinusitis who fail to respond to amoxicillin within 72 hours or severe sinusitis

A

High dose Co-amoxiclav (80-90mkday)

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21
Q

Drug of choice for Frontal sinusitis or severe sinusitis with noted vomiting or poor compliance

A

IV Ceftriaxone

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22
Q

Inflammation of the pharynx that may present as erythema, edema, exudates or enanthem

A

Pharyngitis

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23
Q

Pharyngitis associated with conjunctivitis associated with exposure in swimming pools

Pharyngitis resolves in 7 days
Conjunctivitis resolves in 14 days

A

Pharyngoconjunctival fever

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24
Q

Patient presents with fever, sore throat, EXUDATIVE PHARYNGITIS, &/or PERITONSILLAR ABSCESS
Symptoms persists, neck pain and swelling develops
Patient appears TOXIC

A

Lemierre Syndrome (internal jugular vein septic thrombophlebitis)

Cause by Fusobacterium necrophorum

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25
Unimmunized patient was noted to have bull neck appearance with gray pharyngeal pseudomembrane
Diphtheria
26
Patient,5yr, was noted to have fever and sore throat Pe: erythematous pharynx, enlarged tonsils with white exudates, petechial lesion on the soft palate (DOUGHNUT SIGN), swollen uvula, anterior CLADS
GAS Pharyngitis
27
Drug of choice for GAS pharyngitis in children
Amoxicillin
28
Treatment for eradication of GAS in chronic carriers
Clindamycin (20mkday in 3 doses x 10 days)
29
3-4yrs, boy with recent history of ear infection Present with fever, irritability, decreased oral intake, drooling, neck pain, stridor Noted bulging of posterior pharyngeal wall With CLADS
Retropharyngeal Abscess
30
Definitive diagnosis for pharyngeal abscess
Incision & drainage and culture
31
3 yr old, previous history of throat infection Present with fever, dysphagia, prominent bulge lateral pharyngeal wall with medial displacement of tonsil
Lateral pharyngeal abscess
32
Treatment of choice for pharyngeal abscess
3rd generation cephalosphorin + AmpiSulbactam or Clindamycin
33
Adolescent with recent history of acute pharyngotonsillitis Presents with sore throat, fever, TRISMUS, dysphagia Pe: ASYMMETRIC TONSILLAR BULGE, displacement of uvula
Peritonsillar abscess Tx: surgical drainage and antibiotics for GAS
34
MC cause of bacterial infection in the pharynx
Group A Beta Hemolytic Streptococcus (GABHS)
35
Rapid unilateral enlargement of tonsil Appears grossly normal
Tonsillar neoplasm MC Lymphoma
36
Most common form of acute upper respiratory obstruction Bark-like, brassy cough associated hoarseness, INSPIRATORY STRIDOR, & respiratory distress
Croup
37
Patient present with URTI, rhinorrhea, pharyngitis, mild cough, low grade fever for 1 to 3 days Then develops barking cough, hoarseness, and INSPIRATORY STRIDOR Symptoms are worse at night, and patient prefers to sit up in bed There was noted other family members with mild respiratory illness NECK XRAY: STEEPLE SIGN (subglottic narrowing)
Croup (Laryngotracheobronchitis)
38
Acute course of high fever, sore throat, dyspnea & rapidly progressing respiratory obstruction. There was noted drooling, with neck hyperextended. Patient assumes TRIPOD position (sitting upright, leaning forward with chin & mouth open) No other family members were ill Pe: large, cherry red, swollen epiglottis Neck Xray: THUMB SIGN Patient was noted to be restless
Acute Epiglottitis
39
Mainstay treatment for croup
Airway management Treatment of hypoxia
40
Acute bacterial infection of the upper airway that is potentially life threatening Often follows a viral infection
Bacterial tracheitis
41
Presents with high fever, brassy cough, toxic looking. Patient can lie flat, no drooling, no dysphagia mucosal swelling of cricoid cartilage (major pathologic feature) with copious, thick purulent secretions
Bacterial tracheitis Treatment: Vancomycin or Clindamycin & 3rd generation cephalosphorin (Cefotaxime or Ceftriaxone)
42
MC congenital laryngeal anomaly
Laryngomalacia
43
MC cause of stridor in infants & children
Laryngomalacia
44
Infant presents with inspiratory stridor that worsens with crying and feeding DX & Tx?
Laryngomalacia Tx: expectant observation
45
Presents with BIPHASIC stridor Occurs with a respiratory tract infection Second most common cause of stridor On direct laryngoscopy, reveals a small sized tracheal opening
Subglottic stenosis
46
High pitched inspiratory stridor associated usually with CNS lesions
Bilateral Vocal cord paralysis
47
Presents with aspiration, coughing and choking after a GI surgery. Noted to have weak & breathy cry
Unilateral vocal cord paralysis
48
Abnormal AIR-filled dilation of laryngeal saccule that arises from the false vocal cords to the inner surface of thyroid cartilage. Communicates WITH laryngeal lumen Presents with dyspnea & hoarseness
Laryngocele
49
MUCUS-filled dilatation of the laryngeal saccule DOES NOT communicate with laryngeal lumen Presents with respiratory distress and stridor
Saccular cyst (congeniyal cyst of the larynx)
50
MC location where foreign bodies in the airway are seen
Right bronchus
51
Immediate complication of bronchial foreign body
Air trapping Other features: obstructive emphysema, shift of mediastinum OPPOSITE the side of obstruction
52
2nd MC cause of stridor in neonates MC cause of airway obstruction requiring tracheostomy Usually associated with oversuzed ET tube
Laryngotracheal stenosis
53
MC cause of chronic hoarseness in children
Vocal nodules Causes: 1. Vocal abuse - voice worse at night 2. Laryngopharyngeal reflux - voice worse in the morning
54
MC respiratory tract neoplasm in children
Papillomas
54
MC respiratory tract neoplasm in children
Papillomas
55
MC cause of papillomas in children
HPV 6 & 11
56
3 yr old patient present with chonic hoarseness since 2 years of age but was noted to be increasing in quality. There was noted of mild respiratory distress while playing Prenatal hx: born term via NSD, mother was previously treated for warts DX & TX?
Respiratory Papillomatosis Tx: Endoscopic surgical removal If with recurrence of more than 4 times a year, rapid regrowth with airway compromise or distal multisite spread, need for adjunct therapy (Antiviral eg. Acyclovir, photodynamic therapy, NSAIDS, retinoids, mumps vaccine)
57
Patient presents with first episode of wheezing with associated decreased feeding and tachypnea There was noted family member who has a mild respiratory disease
Acute bronchiolitis
58
Distention of air spaces with IRREVERSIBLE disruption of the alveolar septa
Pulmonary emphysema
59
5mos patient presents with mild tachypnea & wheeze CXR: Distention of left upper lobe, with shift of mediastinum to the right Previous congenital scan revealed problem in the lungs
Congenital lobar emphysema
60
MC site affected by lobar emphysema
Left upper lobe
61
Treatment for Congenital lobar emphysema
Surgery & excision of the lobe
62
Chronic obstructive lung disease of the bronchioles & smaller airways FIBROSIS of the small airways Chest CT: Mosaic pattern of hyperlucency, air trapping & bronchiectasis
Bronchiolitis obliterans
63
Formation of lamellar concretions of CALCIUM PHOSPHATE or "microliths" in alveoli Rare, autosomal recessive Sandstorm appearance in CXR (bilateral infiltrates with fine micronodular appearance) more on the mid &lower lung fields
Pulmonary alveolar microlithiasis (PAM)
64
Complete absence of a lung Associated with VACTERL CXR: unilateral lung collapse, shift of mediastinal structures TOWARDS AFFECTED site Chest CT is diagnostic
Pulmonary agenesis
65
Decrease in the number of alveoli and airway generations Secondary to intrauterine disorders OLIGOHYDRAMNIOS
Pulmonary hypoplasia
66
Consists of hamartomatous or dysplastic lung tissue mixed with normal lung Generally confined to one lobe Can be diagnosed prenatally
Congenital pulmonary airway malformation (CPAM)
67
MC type of CPAM Macrocystic (>5mm cyst) Localized in one part of the lobe Good prognosis
Type I
68
Least common type of CPAM MICROcystic throughout Poorest prognosis Patients usually die at birth
Type 0
69
Earliest clinical signs of pulmonary edema
Increased work of breathing, tachypnea, dyspnea
70
Inflammation of the lung parenchyma
Pneumonia
71
MC bacterial pathogen of pneumonia in children 3wk to 4yr
Streptococcus pneumoniae
72
Pneumonia that occurs for - 2 or more episodes in a year or - 3 or more episodes ever with radiographic clearing in between
Recurrent pneumonia
73
Most consistent manifestation of pneumonia
Tachypnea
74
Hyperinflation with bilateral interstitial infiltrates & peribronchial cuffing Viral or Bacterial pneumonia?
Viral pneumonia
75
Confluent lobar consolidation Viral or Bacterial pneumonia?
Bacterial pneumonia
76
Patient presents with fever, tachypnea, increased work of breathing PE: Crackles bilateral lobe Cxr: bilateral interstitial infiltrates Wbc slightly elevated with LYMPHOCYTIC predominance
Viral pneumonia
77
Patient presents with HIGH fever, tachypnea, increased work of breathing, PE: Crackles right middle lobe, retractions Cxr: right middle lobe consolidation Wbc elevated with NEUTROPHILIC predominance
Bacterial pneumonia Tx: AMOXICILLIN (80-90mkday)
78
Incomplete expansion or complete collapse of air bearing tissue
Atelectasis
79
CXR presents with volume loss and displacemet of fissures; mediastinal structures are displaced TOWARDS AFFECTED side (if massive)
Atelectasis
80
MC cause of pleural effusion in children
Bacterial pneumonia