Pulmonology -10% Flashcards

(54 cards)

1
Q

Acute Bronchiolitis

eti, sxs, dx

A

MCC RSV - fall and winter months

Infants and young children

Sxs:

  • tachypnea
  • respiratory distress
  • expiratory wheezing

Dx:

  • nasal washing for RSV culture antigen assay
  • CXR - normal
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2
Q

Acute Bronchiolitis

Tx

A

Hospitalization if

  • O2 Sat < 95-96%
  • < 3mos old
  • RR > 70
  • nasal flaring
  • retractions
  • atelectasis on CXR

Supportive Tx —>

  • humidified O2,
  • antipyretics,
  • B agonist (albuterol),
  • neb racemic epinephrine, and
  • steroids

O2 is only tx to improve

Ribavirin for severe lung or heart dz in IMC pts

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3
Q

Acute Bronchitis

A

Cough > 5 days; lasts 1-3 wks

MC Viral/Rhinovirus or Coronavirus, Bacterial - M catarrhalis

Chronic Lung pt - H influ, S pneumo, M. catarrhales

Sxs:

  • Cough NO fever ( if + then consider PNA) w/ sputum
  • concurrent URI

Dx - clinical - diffuse lung sounds

  • if focal lung sounds = CXR

Tx:

  • Supportive - NSAIDs, nasal decongestants (Afron), inhaled ipratropium analgesics
  • NO ABX
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4
Q

Acute Epiglottitis

dx, tx

A

X ray lateral film - Thumbprint sign

Secure airway - get cultures for H influ

Tx:

  • intubation
  • supportive care
  • Ceftriaxone* Tx as outpatient if stable
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5
Q

Acute Epiglottitis

eti, sxs

A

EMERGENCY - Supraglottic inflammation

airway obstruction d/t H. influenzas type B (Hib)

MC unvaccinated children

Sxs: 3 Ds of epiglottis

  • Dysphagia
  • Drooling
  • Respiratory Distress
  • tripoding
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6
Q

ARDS

dx

A

ABG PaO2 and FIO2 ratio - not responsive to 100% O2

  • mild 200-300
  • mod 100-200
  • severe <100

CXR

  • bilateral infiltrates => white out pattern
  • spares CP angles

Cardiacs Cath of plum artery

  • Pulm cap wedge pressure (PCWP) < 18 mmHg = ARDS
  • if > 18 mmHg - Cardiopulm edema
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7
Q

Acute Respiratory Distress Syndrome

eti

A

ARDS - respiratory failure characterized by fluid collecting in lungs = no O2

incr permeability of alveolar-capillary membrane -> development of protein rich pulp edema (non cariogenic pulm edema)

can also be d/t critically ill pts or those with significant injuries I.e. sepsis, severe trauma, aspiration of gastric contents, near drowning

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8
Q

ARDS

sxs

A
  • Severe SOB - unable to breath independently w/o ventilator
  • rapid onset of profound dyspnea occurring w/in 12-24 hrs after precipitating event
  • Tachypnea
  • pink frothy sputum crackles
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9
Q

ARDS

tx

A

Tx underlying cause

PEEP lowest setting to maintain PaO2 > 60 mmHg and keep O2 sat > 90%

often fatal

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10
Q

Asthma dx

A
  • PFT - dec FEV1, decr FEV1/FVC ratio
  • Methacholine challenge test >/= 20% dec in FEV1 Bronchodilator test >= 12% incr in FEV1
  • Peak Expiratory Flow Rate used in ED (nl is 400-600) PEFR >15% from initial attempt = response to tx

Severity

  • Intermittent
    • Daytime < 2/wk but <1d; nocturnal = 2/mo
    • FEV1 > 80%
  • Mild Persistent
    • Daytime > 2/wk but <1d; nocturnal > 2/mo
    • FEV1 > 80%
  • Mod Persistent
    • Daily sx; exacerbation >/=2 / wk, nocturnal > 1/mo
    • FEV1 > 60% < 80%
  • Severe Persistent - cont daytime sxs, limited physical activty
    • FEV1< 60%
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11
Q

Asthma

eti

A

Chronic, reversible, hyperresponsiveness, inflammatory airway disease w/ recurrent attacks of breathlessness and episodic wheezing

Sxs:

  • Atopy - eczema
    • asthma’s triad
    • nasal polyps
    • ASA/NSAID allergy
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12
Q

Asthma

sxs

A

SXS: triad of dyspnea, wheezing, cough chest tightness

PE

  • prolonged expiration with wheezing
  • hyperresonance to percussion
  • tachycardia
  • tachypnea

Early Phase

  • Bronchospasm - mucosal edema - minutes to 1-2hrs, responds to bronchodilators

Late Phase

  • mucosal inflammation and incr mucus production, recurrent sxs
  • occurs 4-6 hrs
  • nebs no response
  • need CS tx
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13
Q

Asthma

tx

A

Categorization

Mild intermittent - (<2x/wk or < 2n/mo) -

  • SABA PRN - Albuterol

Mild Persistent (>2x/wk or 3-4 n/mo)

  • low dose ICS daily = Albuterol + Fluticasone (or budesonide - only neb one)

Mod Persistent - (Daily sx or > 1n/wk)

  • Low dose ICS + LABA Daily Med dose ICS + LABA daily
  • Salmeterol or Formoterol (LABA) = never use as monotherapy, usu added to ICS (advair)

Severe Persistent (sx sev x / d and nightly)

  • High dose ICS + LABA qd High dose ICS + LABA + PO steroids

Acute exacerbations O2 Neb SABA Ipatropium bromide PO steroids (5-7 days)

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14
Q

COPD

dx, tx

A

Dx

  • CXR - hyperinflation, parenchymal bullae, blebs are pathogno
  • Spirometry - smokers >45yo, or >10yrs pack year
    • FEV1 / FVC ratio < 0.7, non reversible
  • Gold criteria - all FEV1/FVC < 0.7
    • Gold 1 - FEV1 >80%
    • Gold 2 - FEV 1 > 50 & <79
    • Gold 3 - FEV1 > 30 & < 49
    • Gold 4 - FEV1 <30

Tx - assessment test - CAT <10 (Group A and C)

  • Group A - SAMA or SABA =
    • albuterol or ipatropium = both Atrovent, Combivent
  • Group B - LAMA or LABA or both =
    • Triotropium or Salmeterol - LABA can be used as monotherapy or + LAMA
  • Group C - LAMA > LABA or BOTH or ICS/LABA
  • Group D - LAMA/LABA +/- ICS

Oxygen therapy - only treatment that prolong survival****

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15
Q

COPD

Eti, sxs

A

Chronic Bronchitis - cough > 3 mos for at least 2 years

  • blue bloaters
  • purulent sputum, cyanotic (R sided HF)
  • wheezes common

Emphysema - destruction of alveolar-capillary membrane; thin, smoker

  • *doesn’t smoke (pure emphysema from alpha trypsin deficiency 20-50yo)
  • pink puffers, barrel chested
  • clear sputum, no breath sounds, no cough

Sxs

  • Early dz - tobacco smoke, prolonged expiration, wheezes
  • Late dz - inr AP chest diameter
  • decr tactile fremitus
  • hyperresonance
  • decr breath sounds
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16
Q

Croup

A

Eti:

  • Infection of upper airway - obstructs breathing causing barking cough
  • MCC - parainfluenza virus
  • Children 6mos-3yo, fall - early winter mos

sxs

  • barking cough
  • stridor

dx

  • Steeple sign on PA CXR

tx

  • supportive - air humidifier
  • antipyretics
  • Severe - IV Fluids, neb racemic epi, steroids (Dexamethasone)
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17
Q

Curb-65 Score

A

Hospitalization for Pneumonia Severity

  • Confusion
  • Urea > 7 or BUN > 20
  • RR > 30
  • BP < 90/60
  • Age > 65yo

0-1 = low risk

2 = probable admission vs close outpt mgmt

3-5 = admission & manage as severe

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18
Q

Cystic Fibrosis

A

Autosomal recessive = abn chloride ch transport = altered water andchloride across cells = produce abn mucus that obstructs glands and ducts

Sxs

  • Sinusitis in infancy, nasal polyposis**
  • bronchitis & pneumonia -> bronchiectasis** Pseudomonas
  • Meconium ileus
  • FTT
  • pancreatic insufficiency - steatorrhea
  • infertility M>W

Dx

  • Newborn Screening for CF
    • Quantitative pilocarpine iontophoresis aka Sweat test = incr sodium and chloride levels > 60 mmol/L
    • confirm w/ genetic testing

Tx

  • CF regional center
  • Mucociliary clearance = mucolytics - hypertonic saline and Dnase
    • Chest PT
    • clear pulm infx aggressively
  • pancreatic enzyme replacement
  • psychological support
  • Transplant - option but NOT a cure
  • Spec meds = Ivacaftor, Lumacaftor, Tezacaftor
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19
Q

Foreign Body Aspiration

A

MC in mainstem or lobar bronchus R>L and d/t food

RFs - institutionalization, advanced age, poor dentition, etoh, sedative use

Sxs: Presentation depends on location of obstruction

  • Inspiratory stridor - high in airway
  • wheezing and decr breath sounds - low in airway

Dx

  • Expiratory CXR - hyperinflation to affected side
  • ABG - eval ventilation

Tx

  • Remove foreign body with bronchoscope
  • Rigid bronchoscopy in children
  • Flexible is diagnostic and therapeutic in adults
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20
Q

Hemoptysis

eti, sxs

A

Coughing up blood - airway bleeding

MCC

  • Bronchitis - hemoptysis, dry cough, cough with phlegm
  • Tumor mass - hemoptysis, chest pain, rib pain, tobacco hx, wt loss, clubbing
  • Tuberculosis - hemptysis, chest pain, sweating

Sxs:

  • blood stained mucus or blood from bronchi, larynx, trachea, or lungs
  • Bronchial capillaries rupture d/t acute infx (viral/bacterial bronchitis, bronchiectasis, cig smoking)
  • Tiny blood vessles broken
  • Vascular engorgement w/ erosions in Pulm HTN or masses
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21
Q

Hemoptysis

dx, tx

A

Dx

  • Cytology
  • Sputum/expectorant examination
  • Fiberoptic bronch - for CA tissue
    • biopsy
    • bronchial lavage
    • brushing
  • Rigid bronch - massive bleeding - better suctioning and airway maintenance capabilities
  • High Res CT - pathophys

Tx

  • massive hemoptysis - aggressive early consult with pulmnologist
  • ABCs - airway maintenance is vital - primary COD d/t aspyhixation
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22
Q

Horner’s Syndrome (Lungs CA)

A

Cervical sympathetic chain

  1. unilateral facial anhidrosis (no sweating)
  2. ptosis
  3. miosis
23
Q

Hyaline Membrane Disease

A

Premature infants - babies born before lungs are producing enough surfactant.

MCC respiratory disease in preterm babies < 30wks

Sxs

  • tachypnea
  • intercostal retractions
  • SOH w/ grunting sounds
  • nasal flarings

Dx

  • resp acidosis
  • CXR - ground glass appearance, diffuse bilat atelectasis

Tx

  • antenatal steroids 24-48 hrs of birth - bethametasone IM x 2
  • artificial surfactant through endotrach tube
  • Mech vent PP
24
Q

Idiopathic Pulmonary Fibrosis

Restrictive Pulm diseases

A

Chronic progressive lung disorder from increase scarring = reduces Lung capacity

MC all interstitial lung disease

Sxs

  • DOE
  • Thoracic pain + dry cough
  • Inspiratory crackles, clubbing of fingers

Dx

  • PFT = decr lung volume and normal FEV1/FVC ratio; restrictive
  • CXR - fibrosis
  • CT = diffuse patchy fibrosis, honey combing, ground glass opacities

Tx

  • Corticosteroids, O2
  • eventually lung transplant * only cure
25
Influenza
Viral respiratory infx by orthomyxovirus (three strains A, B, C) sxs * fever, **coryza**, cough, headache, malaise * uncomplicated - body aches and fever * complicated - dyspnea + above Dx * rapid **antigen test** in clinic * rapid serology more accurate * CXR - **bilateral diffuse _infiltrates_** Tx * symptomatic for most * antivirals w/in \< 48 hrs * Tamiflu/**Oseltamivir** or Zanamivir/Relenza for influ A & B * Zanamivir - c/i in kids \< 7yo powder * Prevent yearly vaccine - trivalent/quadvalent killed or live attenuated intranasal * Gullain Barre or egg allergy
26
Light's Criteria
Pleurocentesis to determine if Pleural fluid is exudative: 1. Pleural fluid protein / serum protein \>0.5 2. Pleural fluid LDH / Serum LDH \>0.6 3. Pleural fluid LDH \> 2/3 ULN serum LDH Exudative - infection, malignancy, immune, MCC - pna, CA, PE, TB
27
Lung Cancer - Adenocarcinoma
35-40% of cases MC type of bronchogenic carcinoma 30-40% MC mucous cells **_non-smoker_** w/ incidental finding and small **_peripheral_** lesion
28
Lung Cancer - Carinoid
1-2% tumor that produces excess serotonin (niacin B3 deficiency) Pink purple leasion in the central airway resistant to chemo/radiation surgical excision
29
Lung Cancer eti, sxs, dx
Two major categories 1. Small Cell Lung Cancer (SCLC) - 15% and poor prognosis 2. Non-Small Cell Lung Cancer (NSCLC) - 85% * Ad * adenocarcinoma​ * squamous cell carcinoma * large cell carcinoma * carcinoid tumor Sx * Cough * Dyspnea, * chest pain * hemoptysis - airway involvement * Wt loss - B signs - weight loss, fever, nt swts Dx * CXR to screen * **Bronchoscopy and biopsy or FNA - gold standard** * Squamous Cell or SCLC - central mass * Adenocarcinoma - peripheral mass * LC and Carcinoid - throughout lungs * TNM Staging
30
Lung Cancer - Large Cell
rare 5% rapid doubling time rarely response to surgery peripheral
31
Lung Cancer - SCLC
15% ; Highly aggressive always occurs in smokers rapidly growing, mets by dx ; **mediastinal mass** **_cannot be tx with sx, needs chemo/XRT_** a/w * ACTH and ADH - hyponatremia and hypercalcemia * Lambert-Eaton myasthenic syndrome - muscle weakness of limbs d/t ACTH/ADH * SVC syndrome * Horner syndrome * SIADH - decr Na
32
Lung Cancer - Squamous Cell Carcinoma
25-35% of cases Bronchial in origin and centrally located mass MC in smokers likely to have **persistent cough, recurrent PNA,** **hemoptysis,** **central bronchus** solitary tumor **\*\* Hypercalcemia \*\* paraneoplastic syndrome**
33
Lung Cancer Treatment
_NSCLC_ Surgical resection Adj chemo and Radiation if advanced (Stage 4 = palliative (mets) _SCLC_ **chemo only** 5 year prognosis = 15%
34
Pancoast Syndrome
A/w Squamous Cell Carcinoma tumor at lung apex, apical mass crushes **brachial plexus** + **cervical sympathetic chain** * Shoulder pain * UE weakness * **Horner's syndrome - miosis, anhidrosis, ptosis**
35
Pertussis
Whooping cough - severe hacking cough followed by high pitched intake of breath (sounds like whoop) Gram neg bacteria = **Bordetalla pertusis** Consider in **adults with cough \> 2 wks**, patients \< 2yo 1. catarrhal stage - cold like sxs, poor feeding, sleeping 2. Paroxysmla stage - high pitched **inspiratory whoop** 3. Convalescent stage - residual cough (100 days) Dx - Nasopharyngeal swab of secretions and culture Tx - with M**acrolide (clarithomycin/azithromycin)** * supportive care w/ steroids + B2 agonists * vaccinations * 5 doses - 2, 4, 6, 15-18mos, 4-6 yrs (DTap) * 11-18 yo = 1 dose Tday * Expectant mothers Tdap each pregnancy at 27-36 wks
36
Pleural Effusion
Accumulation of excess fluids in pleura space Sxs * dyspnea * vague discomfort or sharp pain that worsens during inspiration * **decrease tactile fremitus, decr absent breath sounds** Dx * Determine whether pleurocentesis * **exudative** (infection, malignancy, immune) or * **transudative** (transient changes in hydrostatic pressure - cirrhosis, MCC CHF, nephrotic syndrome, ascites, hypoalbuminemia * **Lateral decubitis CXR** * Isolated L Pleural effusion = exudative * R sided = transudative * Chest CT * **US - guided thoracentesis - gold** Tx * **Thoracentesis**
37
Pleuritic Chest Pain
Inflammation of tissues that line lungs and chest cavity (pleura) sudden, intensely sharp , stabing, burning pain in chest when inhaling and exhaling exacerbated by deep breathing, coughing, sneezing, or laughing **MCC - PNA, pericarditis, pericardial effusion, pancreatitis**
38
Pneumonia - Bacterial
**S pneumo \> H influ \> Moraxella catarrhalis** = show on gram stain **Atypical - Legionella, Mycoplasma pneumo, Chlamydophila pneumo** Sxs * fever, dyspnea, cough, myalgias, rigors/sweat, new cough * +/- sputum - rust - pneumococcal * *S pneumo* - single rigor, pleurisy * *H influ* - underlying COPD * *Legionella* - **high fever**, hypoNa, bad abd pain + diarrhea, appears more ill than CXR * *M. pneumo* - walking pneumo, extrapulm sxs **bullous myringitis (bloody TM)** Dx * CXR - Patchy, segmental **lobar**, multilobar **_consolidation_** * Blood cultures x 2 - only inpatient * Sputum gram stain Tx * Outpatient - **macrolides (azithromycin**), **_Doxy,_** resp FQ (Levofloxacin) * Pneumococcal =\> ​tx until pts afebrile for 72 hrs (x5d) * atypical pna (legionella, pertussis) =\> x 2-3 wks * Inpt - **_Ceftriaxone + azithromycin_**, or resp FQs * Prevnar and Pneumovax - vaccines
39
PNA - Fungal
Common in IMC pts (AIDS, steroid use, organ transplant) _Coccidiodes_ (valley fever) * non remitting cough/bronchitis non responsive to conventional tx * Fungal inhalation in **Western States** * Dx with ELISA for IgM and IgG * Tx with **fluconazole/itraconazole** _Pulmonary aspergillosis_ - health immune systems * **fluconazole/itraconazole** _Cryptococcus_ - soil, disseminate and amenintitis * LP for meningitis * Tx with **amp B** _Histoplasmosis_ - apical pulmonary lesions resembling cavitary TB, worsening cough and dyspnea, progression to disabling respiratory dysfx * **bird or bat droppings** - Mississippi Ohio River Valley * Signs - mediastinal or hilar LAD (sarcoid) * tx with **amp B** _HIV - PJP (Pneumocystis jiroveci)_ -Common in HIV pts with CD4 count \< 200 * CXR - diffuse interstitial or bilateral **perihila**r infiltrates * dx - bronchoalveolar lavage PCR, labs, HIV tests, low O2 despite supplemental oxygen * Tx with **bactrim** and steroids
40
PNA - Viral
Adults - Flu MC Kids - RSV quick onset Dx * CXR - bilateral interstitial infiltrates * rapid antigen testing for flu * RSV nasal swab * cold agglutinin titer negative Tx * Flu with Tamiflu (A & B) if sxs \< 48hrs onset * symptomatic tx = B2 agonists, fluids, rest
41
**Pneumoconiosis** Restrictive Lung Diseases
Pulmonary fibrosis with a known cause **Abestosis** * Insulation, demolition, construction * CXR - reticular, linear pattern, w/ basilar predominancy, opacities, honeycombing * can turn into mesothelioma **Coal Workers** * coal mining, * Nodular opacity in upper lung fields; hilar adenopathy not necessarily prominent **Silicosis** * mining, sandblasting, stone or quarry work * **eggshell calcification of hilar nodes** * incr risk of TB and progression to massive fibrosis **Berylliosis** * high tech fields, nuclear power, ceramics, foundries * diffuse infiltrates, **hilar adenopathy** * req's chronic steroids
42
Pneumothorax
Collapsed lung caused by accumulation of air in pleural space _Spontaneous vs traumatic_ * primary - abs of underlying dz (tall, thin, male age 10-30 at greater risk), smoker * Secondary - presence of underlying dz (**COPD,** asthma, CF, ILD) _Acquired_ * Iatrogenic * Traumatic -\> penetrating or blunt trauma * Barotrauma - mechanical ventilation SXS: * Acute onset ipsilateral chest pain and dyspnea - **decreased tactile fremitus** * deviated trachea * **hyperresonance** * Diminished breath sounds Tx - depends on size * **small \< 15%** of diameter of hemithorax - resolves spontaneously w/o chest tube placement * **large \> 15%** diameter & symptomatic - chest tube placement * Serial CXR q 24 hrs until resolve
43
Pulmonary Embolism eti, sxs
blockage in one of pulmonary arteries in lungs MCC - deep veins of LEs RF: * Virchow's Triad * Hypercoagulable state (sx, CA, OCP, preg, smoking, long bone fracture) * Venous stasis * Epithelial injury Sxs * Dyspnea MC * pleuritic chest pain * Tachycardia --\> EKG with **S1Q3T3, non spec ST waves** * Tachypnea
44
Pulmonary Embolism Treatment
**Hemodynamically stable** 1. Anticoags * **UFH or LMWH =\> Warfarin** - 3 mos bridge with heparin 3-5 days * INR range 2-3 * LMWH and hep for cancer and pregnant patients\*\* * factor Xa inhibitors **Rivaroxaban or** PO Direct Thrombin Inhibitors **Dabigatran** * Minimal antigoag for 3 mos w/ reversible RFs * if unprovoked - 6 mos then reeval * If two eps unprovoked - long term anticoag 1. **IVC filter -** stable pt who can't take anticoags or unsuccessful UNSTABLE 1. **Thrombolectomy** - if unstable or massive PE
45
Respiratory Syncytial Virus
MCC LRTI in children - get by age 3 leading cause of PNA and bronchiolitis sxs * Rhinorrhea * wheezing/coughing that persists for months * low grade fever * nasal flaring/retractions * nail bed cyanosis Tx * hospitalization if * tachypnea w/ feeding difficulties * visible retractions * O2 Sat \<95% * Supportive care * albuterol via neb * antipyretics * humidified O2 * Steroids (controversial) * Resolves in 5-7 days Vaccines for children with lung issues or premature --\> **synagis prophylaxis (palivizumab)** 1x/m for 5 mos in Nov
46
Sarcoidosis ## Footnote **Restrictive Lung Disease**
Granulomatous disease =\> **noncaseating granulomas** that affects multiple organ systems 20-40yo, Northern europeans or AAs Sxs * fever, weight loss, arthralgias, erythema nodosum Dx * Hypercalcemia; **ACE levels x 4 UNL** * ele ESR * Biopsy of peripheral lesions or fiberoptic bronch for central pulm lesions * Serial PFT for progression Tx * Corticosteroids, methotrexate, immunosuppressive meds * ACE-I for periodic HTN
47
Screening for Lung Cancer
**USPSTF** **Annual low dose CT, if** * 55-80 yo * \>30 pack year hx * current smokers or * quit within last 15 years Incidental finding on CXR * send for CT * if suspicious - need bx * Ill defined borders, lobular or spiculated = cancer * If not suspicious \< 1cm * monitor q 3mos, 6 mos, yearly for two years * calcifications, smooth, well defined edges = benign Mets- Adeno and Small cell = BRAIN METS bone
48
SVC Syndrome
a/w SCLC obstruction of SVC by tumor resulting in * facial fullness * JVD * dilated veins in anterior chest
49
Tension PTX
penetrating injury -\> air in pleural space increasing and unable to escape **_Mediastinal shift leading to TRACHEAL deviation to contralateral side or severe JVD_** CXR = pleural air ABG = hypoxemia medical emergency - large bore needles to allow air out of chest **Needle decompression - 2nd ICS, midclavicular line, above rib**
50
Tuberculosis eti, sxs, dx
**Mycobacterium tuberculosis** RF - endemic area, IMC (HIV), recent immigrants (\<5yo), prisoners, health care workers transmission - inhalation of aerosolized droplets Sxs: * fatigue, productive cough, **bloody sputum** * **night sweats**, wt loss, post tussive rales * miliary TB = spread outside lungs - neuro or GI * vertebral column (Pott disease) Dx: * **Sputum for AFB smears** - have to be 3 AFB negatives * NAAT - quicker dx * CXR - cavitary lesions, infiltrates, **ghon complexes** in **apex of lungs** * Bx - **caseating granulomas**
51
Tuberculosis Treatment
_Empiric tx_ PPD + & CXR negative - **latent TB** =\> **Isoniazid 9 mos +B6 for neuropathy** PPD + & CXR positive - active TB =\> quad therapy (RIPE) x2 mos, then 2 drugs for 4 mos * **Rifampin** - red orange urine, hepatitis * **Isoniazid** - perip neuropathy (B6 pyridoxine 25-50mg/day) * **Pyrazinamide** - hyperuricemia (gout) * **Ethambutol** - optic neuritis (eye changes), red green blindedness _Need two negative AFB smears and cultures to stop therapy_ Prophy isoniazid for household members - for 1 year dc therapy if transaminases \> 3-5 x ULN
52
**Tuberculosis** Screening
PPD - Tb skin test **Mantoux Test Rules** - tests positive if * \>5mm at high risk, fibrotic changes on CXR, IMC HIV/Drugs, steroids/TNF antagonist daily, or close contact w/ infectious TB * \> 10mm in pts \< 4yo, and risk factors = health care facilities, IVD, recent immigrants with high prevalence, renal insufficiency, prison, homeless shelter, bypass surgery * \> 15mm if no other risk factor
53
Well's Criteria
54
PE - dx
Negative suspicion - rule out