Pulmonology Flashcards

(98 cards)

1
Q

Post-Viral Cough

A
  • aka post-infectious cough
  • no specific etiological agent
  • cough lasting from 3-8 weeks following a viral URI or bronchitis
  • usually normal CXR
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2
Q

Chronic Cough

A
  • cough lasting > 8 weeks in adults
  • cough lasting >4 weeks in children
  • can be sign of underlying condition:
    • GERD
    • ACE inhibitor use (lisinopril)
    • asthma
    • upper airway cough sundrome
    • sarcoidosis, TB, cancer
  • CXR to r/o other causes
  • if cause can’t be identified:
    • consider chest CT scan
    • pft
    • refer to pulmonologist
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3
Q

Chronic Bronchitis

A

“Blue Bloaters”

  • chronic cough with phlegm for 3months of the year for 2+ years → without acute cause
  • PE: crackles and wheezes, percussion = normal
  • Dx: FEV1/FVC = <0.7
    • increased HGB and HCT → chronic hypoxemia
    • CXR: peribronchial and perivascular markings
  • TX: SABAs for mild, LAMA for moderate-severe or LABA +/- ICS
    • SAMA (ipratroprium) = main inhaler for COPD
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4
Q

COPD definition

A

chronic bronchitis + emphysema

proteases > anti-proteases

Causes: smoking, pollution, chronic damage to lungs, family hx, occupational exposure to dust, vapors, fumes and other chemicals, childhood factors (frequent respiratory infx, low birth weight)

alpha 1 antitrypsin deficiency

Post-bronchodilater FEV1/FVC must be <0.7 for a diagnosis by GOLD criteria

tend to be >40 years old

for acute exacerbation aim for SpO2 of 88-92%

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5
Q

Emphysema

A

part of COPD

“Pink Puffers”

  • enlarged air spaces as a result of damage to alveolar septae → decreased lung function → chronic hyperventilation
  • S/sxs: quiet lungs, thin, barrel chest, minimum sputum, underweight, pursed lips to increase resistance of exhale
  • PE: diminished breath sounds, prolonged expiration, and diminished heart sounds, hyperresonance on percussion
  • Dx:
    • CXR: loss of lung markings, hyperinflation, flattened diaphragm, small thin appearing heart
    • subpleural blebs = pathognomonic
  • Tx: SAMA (ipratropium bromide) or albuterol inhaler
    • oxygen
    • PO steroid burst during exacerbation
    • abx if increased sputum production, increased purulence, or increased dyspnea
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6
Q

Acute Bronchiolitis

A

Most commonly caused by RSV in fall and winter

  • common in infants and children
  • S/sxs: wheezing, tachypnea, respiratory distress, fever
    • often have prodromal viral sxs (fever, uri) for 1-2 days followed by respiratory distress
  • PE: expiratory wheezes, may have normal serous nasal discharge
  • Diagnosis: CXR = normal
    • test for influenza, RSV (antigen test or nasal washing monocloncal antibody test)
  • Tx: Supportive tx → humidifed air, antipyretics, beta-agonists, nebulized racemic epi
    • oxygen = mainstay of tx
    • Palivizumab prophylaxis (Synagis) for immunocompromised, premature infants etc
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7
Q

Acute Bronchitis

A

cough > 5 days, can last 1-3 weeks

most often viral (95%), but bacterial = Moraxella, S. pneumo, chlamydia pneumoniae

  • S/sxs: cough >5 days, low fever, malaise, dyspnea, URI sxs
    • may have hemoptysis (most common cause of hemoptysis, followed by carcinoma)
  • PE: less severe than PNA (normal vitals) no crackles or egophany
    • may have rhonchi or wheezing
      • rhonchi that clears with cough
  • Dx: clinical, can obtain CXR if uncertain
  • Tx: supportive → fluids, rest, corticosteroids if underlying RAD
    • Dextromethrophan (Tessalon Pearls)
    • Guaifenesin (robitussin)
    • SABAs for wheezing
    • antipyrettics
    • Ribavirin if severe lung or heart disease
    • if O2<96% on RA→ hospitalize
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8
Q

Acute Epiglottitis

A

Medical Emergency → usually caused by Hflu

Males> females, DM =risk factor in adults; most common in age 3mo-6yr

  • S/sxs: fever, odynophagia (pain with swallowing), Tripoding , dyspnea
    • 3Ds: drooling, dysphagia (difficulty swallowing), Respiratory distress
  • PE: inspiratory stridor**, muffled hot-potato voice, hoarseness, **Thumb print sign
  • Diagnosis: laryngoscopy
  • tx: secure airway then cx for Hflu
    • intubate if necessary, supportive care
    • ceftriaxone (or 2nd or 3rd gen cephs)
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9
Q

Acute Laryngotracheitis

A
  • aka Croup
  • **barking cough most commonly caused by parainfluenzae virus**
  • abrupt onset of symptoms
  • **Steeple Sign**
  • home treatment: symptomatic care maybe with some dexamethasone
  • Nebulized epi with IV/oral/IM dexamethasone
  • **the WESLEY CROUP SCORE** >12 → send to the hospital
    • mild = 2
    • Moderate 3-7
    • severe >/= 8
    • impending respiratory failure >/=12
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10
Q

Step 1 therapy for Asthma in Adults

A

sxs < 2x/month

  • Controller:
    • TAke ICS whenever SABA is taken
  • Reliever:
    • SABA
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11
Q

SABA

A

short acting beta agonist

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12
Q

Step 2 therapy for Asthma in Adults

A

sxs 2x/month + but less than 4-5days/week

  • Controller:
    • low dose maintenance ICS
  • Reliever:
    • PRN SABA
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13
Q

ICS

A

inhaled corticosteroid

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14
Q

Step 3 Therapy for Asthma in Adults

A

sxs most days, or waking with asthma once/week +

  • Controller:
    • low dose maintenance ICS-LABA
  • Reliever:
    • PRN SABA
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15
Q

LABA

A

long acting beta 2 agonist

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16
Q

LTRA

A

leukotriene receptor antagonist

i.e. singulair (montelukast)

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17
Q

Step 4 Therapy for Asthma in Adults

A

sxs most days, or waking with asthma once/week+, or low lung function

  • Controller:
    • medium/high dose maintenance ICS-LABA
  • Reliever:
    • PRN SABA
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18
Q

Step 5 Therapy for Asthma in Adults

A
  • Controller:
    • add on LAMA
    • refer for phenotypic assessment
    • +/- anti-IgE, anit-IL5/5R, anti-IL4R
    • consider high dose ICS-LABA
  • Reliever:
    • PRN SABA
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19
Q

Age for pediatric asthma tx

A

6-11 years old

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20
Q

Step 1 therapy for Asthma in Peds

A

sxs <2x/month

  • Controller:
    • low dose ICS whenever SABA is taken; or daily low dose ICS
  • Reliever:
    • PRN SABA
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21
Q

Step 2 Therapy for Asthma in Peds

A

sxs 2x/month+ but less than daily

  • Controller:
    • daily low dose ICS
    • other:
      • daily LTRA, or low dose ICS taken whenever SABA taken
  • Reliever:
    • PRN SABA
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22
Q

Step 3 Therapy for Asthma in Peds

A

sxs most days, or waking with asthma 1x/week+

  • Controller:
    • low dose maintenance ICS-LABA or medium dose ICS
    • Other:
      • low dose ICS + LTRA
  • Reliever:
    • PRN SABA
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23
Q

Step 4 Therapy for Asthma in Peds

A

sxs most days or waking with asthma 1x/week + AND low lung function

  • Controller:
    • medium dose ICS-LABA and refer for expert advice
    • other:
      • high dose ICS-LABA, or add on tiotropium or add on LTRA
  • Reliever:
    • PRN SABA
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24
Q

Step 5 Therapy of Asthma for Peds

A
  • Controller:
    • Refer for phenotypic assessment + add-on therapy. e.g. anti-IgE
    • other:
      • add-on anti-IL5, or add on low dose OCS but consider side-effects
  • Reliever:
    • PRN SABA
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25
SABAs
Short acting beta-2 agonists * albuterol * levalbuterol * metaproterenol * Terbutaline
26
Albuterol (Proventil-HFA; Proair-HFA)
SABA: MDI and neb * _dosing_: 2puffs Q4-6hours (90mcg/puff) * stimulates beta-2 receptors = bronchial muscle relaxation * _SEs_: **_HypoK_** especially during continuous neb * beta-2 stimulation causes cellular uptake of K+ = decreased srum K+ * also **tachycardia** (because not very selective and will stimulate beta-1 receptors)
27
Levalbuterol (Xopenex-HFA)
SABA: MDI and neb * steroisomer of albuterol, but higher affinity for beta-2 so less sysstemic sympathetic effects = b/c less binding to beta-1 * _SEs_: **_HypoK_**
28
Metaproterenol (Alupent)
SABA: PO * _SEs_: palpitations * tachycardia * **hypoK** * tremor * HA, nausea, nervousness
29
Terbutaline
SABA: PO or pareneteral (SQ injection) * often used for acute attack (**0.25mg SubQ**) * _SEs:_ * SABA * tocolytic * **not approved for children \<6yo**
30
LABAs
long acting beta-2 agonists * salmeterol DPI (Serevent Diskus) * Formoterol DPI (Foradil) * Arformoterol (Brovana) * not for kids * Indacaterol (Arcapta) * not for kids * Olodaterol (striverdi Respimat) * (**Some Fish Are Inherently Odorous)**
31
Salmeterol DPI (Serevent Diskus)
LABA **do not use as monotherapy** * partial agonist
32
Formoterol DPI (Foradil)
LABA * helpful for nighttime sxs * full agonist * onset = to that of albutero but DO NOT USE FOR ACUTE BRONCHOSPASM * _SEs:_ **paradoxical bronchospasm**
33
Arformoterol (Brovana)
LABA: neb * used for **COPD only!!** * 2x more potent than formoterol * _SEs:_ * _​_**paradoxical bronchospasm** * palpitation/tachy/tremor * lightheadedness/nervousness/HA/nausea * **NOT APPROVED FOR CHILDREN**
34
Indacaterol (Arcapta)
LABA: DPI * for COPD * _SEs_: * **paradoxical bronchospasms** * palpitations/tachy/tremor * nervousness/lightheadedness/HA/nausea * **NOT APPROVED IN CHILDREN**
35
Olodaterol (Striverdi Respimat)
LABA: inhaler * **Long half life!!** t1/2 = 45hours * *2C9 substrate =* increased side SEs * plus Same SEs as other LABAs
36
Inhaled Corticosteroids (ICS)
MOA: inhibit inflammatory cells (mast cell, eosinophils, neutrophils) and cytokines (histamine, leukotriens) **\*\*Flat dose response curve = double the dose adds limited additional effect \*\*** **BID Dosing is better (need more in smokers)** * Beclomethasone HFA (QVAR) * Budesonide DPI (Pulmicort) * Ciclesonide (Alvesco) * Fluticasone HFA (Flovent) * Fluticasone DPI (Flovent Diskus) * Flunisolide (Aerobid) * Mometasone DPI (Asmanex) * _SEs_: * oral candidiasis * cough * Dysphonia * Adrenal Suppression (at high dose)
37
Omalizumab (Xolair)
monoclono- **anti-IgE antibody** * stops release of inflammatory mediatorys * used for moderate to severe asthma * **significantly reduces ICS use** * SQ injection * _SEs:_ * injection site rxn, bruising, redness, pain, stinging, itching etc * anaphylaxis (rare) * monitor 2 hours after injection for 3 months then 30 min thereafter
38
Combined ICS/LABA
* Fluticasone/Salmeterol (Advair) DPI * Fluticasone/Vilanterol (Breo Ellipta) * +3A4 inhibitors (both advair and breo) = increased LABAs = **QT prolongation** * Budesonide/Formoterol HFA (Symbicort) * Mometasone/Formoterol (Dulera) * _SEs_: Thrush * dysphonia * pharyngitis * HA * nausea * tremor
39
GOLD 1-4
for COPD * Gold 1: FEV1 \>80% * mild * Gold 2: FEV1 50-79% * moderate * Gold 3: FEV1 30-49% * severe * Gold 4: FEV1 \<30% * very severe
40
ABCD categorization of COPD
41
Stage A COPD Tx
* First Line: * SABA prn or SAMA prn (bronchodilators) * Second Line: * LAMA or LABA or SABA + SAMA
42
Stage B COPD Tx
* First line: * LAMA or LABA (long acting bronchodilators) * Second Line: * LAMA + LABA
43
Stage C COPD Tx
* First line: * ICS + LABA or **LAMA** * Second Line: * LAMA + LABA * LAMA + PDE4i * LABA + PDE4i
44
Stage D COPD Tx
* First Line: * ICS + LABA and/or LAMA * Second Line: * ICS + LABA and LAMA * ICS + LABA and PDE4i * LAMA + LABA * LAMA + PDE4i
45
Phosphodiesterase (PDE)-4 inhibitors
inhibit breakdown of cAMP = reduction of inflammation **Roflumilast (Dalirespt)** * for prevention of COPD * _SEs_: * diarrhea, decreased appetite, weight loss, abdominal pain * headache, insomnia * anxiety and depression * DDI: CYP 1A2 and 3A4 * inducers: butalbital, phenytoin, rifampin, carbamazepine (avoid use) * inhibitors: amiodarone, clarithromycin, cimetidine, ketoconazole (use with caution)
46
Most common bacterial organisms associated with mild exacerbation of COPD and More Severe COPD
* Mild: * strep pneumo, H.flu, Moraxella * Severe: * E.coli, Klebsiella, enterobacter, pseudomonas
47
Pseudomonas risk factors
1. 4 or more courses of abx over the past year 2. recent hospitalization (2+ days in past 90) 3. isolation of pseudomonas during a previous hospital visit 4. severe underlying COPD 1. FEV1\<50
48
Mepolizumab (Nucala)
monoclondal antibody that **targets** **IL-5** * IL-5 stimulates matural and release of eosinophils in bone more = inflammation * Indication: maintenance tx of severe asthma **age \>/=12 yo** * _SEs_: * anaphylaxis, angioedema, bronchospasm, hypotension, urticaria, rash * herpes zoster has occurred: IZ if appropriate prior to starting therapy
49
Reslizumab (Cinqair)
monoclonal antibody **against IL-5** * _indications_: add on maintenance tx with severe asthma for **\>/= 18 yo** and an eosinophilic phenotype * IV infusion only * _SEs_: * **anaphylaxis, malignancy** * CPK electation = adverse muscle related rxns * oropharyngeal pain
50
Methylxanthines
**theophylline** inhibit phosphodiesterase = bronchodilation * less effective than ICS * narrow therapeutic index 5-15mcg/mL * metabolized by CYP 1A2 and 3A4 * DDI: inducers: carbamazeine, phenytin, rifampin, ST. John Wort * inhibitors: clarithromycin, telithromycin, ketoconazole, itraconazole, voriconazoe, grape fruit juice * _SEs_:cardiac arrhythmias, seizures
51
LAMAs
long acting muscarinic antagonists * Tiotroprium * alcidinium * glycopyrrolate * Umeclidinium
52
SABA + Anticholinergic
* Albuterol/Ipratroprium (Combivent Respimat) * Duoneb * _SEs_: paradoxical bronchospasm * palpitations/tremor/tachy * **CONTRAINDICATION: soy or peanut allergy** * NOT for Children
53
Leukotriene Inhibitors
only for asthma (LTRA) * montelukast (Singulair) * Zileuton (Zyflo) * SEs: **hepatotoxicity** * DDIs: * **inducers**: rifampin, carbamazepine, St. John's wort * **inhibitors**: fluconazole, amiodarone, fluvoxamine, metronidazole, voriconazole
54
Omalizumab (Xolair)
immunomodulator (**anti-IgE antibody**) * inhibits biding of IgE onto mast cells and basophils = stops release of inflammatory mediators mainly used in COPD, but also for moderate-severe asthma * SQ injects Q2-4 weeks **in clinic**, must be observed 2 hours after injection x 3months, then 30 min thereafter. * significantly reduces use of ICS
55
Abx for COPD exacerbation outpt (⅓ cardinal sxs)
Mild, no abx needed cardinal sxs: increased dyspnea, sputum volume, or purulence
56
Abx for COPD exacerbation outpt (⅔) no risk factors
macrolide 2nd and 3rd gen ceph doxy Septra (TMP/Sulfamethoxazole)
57
Abx for COPD exacerbation outpt (⅔ cardinal signs) with risk factors
respiratory FQs (moxi/levo/gemi) Amoxicillin/Clavulanate (Augmentin)
58
Abx for COPD exacerbations in hospital (⅔ of cardinal) with risk factors for pseudomonas
FQ (levo PO or IV) Cephalosporins (Cefepime IV or Ceftazidime IV) Zosyn IV (piperacillin + tazobactam)
59
Abx for COPD exacerbations in hospital (⅔ cardinal) with no pseudomonas risk
FQ (levo or Moxi) Cephalosporins (ceftriaxone or cefotaxime)
60
Complicated COPD
FEV1\<50% age \>65 \>/= 3 exacerbations/year cardiac disease
61
Influenza
ssRNA Hemagglutinin spikes→ allow virus to bind to host(targeted by IZs) , neuraminidase→ allow virus to bud (targeted by meds) * S/sxs: **sudden onset** high fever, chills, malaise, sore throat, headache, and coryza, **myalgias** (especially legs and lumbosacral), non-productive cough * **_classic triad: FEVER, DRY COUGH, MYALGIAS_** * PE: ill appearance, mild pharyngeal edema, cervical adenopathy +/-, serous nasal drainage * Dx: **rapid antigen test**, serology = more accurate, WBC does not correlate well with severity → often normal or low (if \>15K → suggests secondary bacterial) * Tx: mild disease & healthy? → supportive tx (acetaminophen, fluids, and rest) * hospitalized or at-risk? → neuraminidase inhibitors (Oseltamivir or Zanamivir (Dr. Oz txs the flu)) → need to be initiated within 48 hours of onset * empiric antiviral tx: children \<2, pregnant, 65+, women up to 2 weeks post-partum, chronic or immunosuppressed
62
Pertussis
aka Whooping Cough → causative agent **bordetella pertussis** → gram -, coccobacillus common in children \<2 yrs, respiratory droplet transmission * S/sxs: consider in adults with cough \> 2weeks * _catarrhal stage_: cold like sxs, poor feeding and sleeping * _paroxysmal stage_: high-pitched **inspiratory whoop** *between coughing fits* → post-tussive emesis is highly indicative of this infx * _convalescent stage_: residual cough (up to 100 days) * Dx: nasopharyngeal swab for cx and PCR * Tx: supportive care +/- steroids/SBAS * **Macrolides** (clarithromycin, azithromycin) * DTaP, TDap Izs * Complications: **PNA**, encephalopathy, otitis media, sinusitis, seizures
63
Bacterial Pneumonia
Causative Agents: **S. Pneumo (rusty color sputum**, common in after splenectomy), **S. aureus (salmon colored sputum**, lobar, after influenza), Hflu, **Klebsiella (alcohol abuse; currant jelly sputu**m, aspiration); atypicals → **mycoplasma (young ppl living in dorms**, (+) cold agglutination), **chlamydia (college kids**, sore throat), **legionella (air conditioning**, low Na+, GI sxs and high fever) * S/sxs: tachycardia, tachypnea, **fever**, pleuritic chest pain, dyspnea +/- rigors (associated with strep pneumo) * PE: CXR: **infiltrate/consolidation** * Typical: percussion → dull, increased tactile fremitus, egophony and crackles * atypical: pulmonary exam is often normal (may have crackles) * Dx: CXR, **blood cxs x 2** , sputum gram stain * Tx: outpt → **doxycycline, macrolides (500mg 1st day, then 250mg for days 2-5)** * CURB-65: Confusion, uremia (BUN \>19), RR \>30, BP \<90/\<60, age 65+ * inpatient tx: * **ceftriaxone + azithromycin, respiratory fluoroquinolones** (Moxi, levo)
64
RSV
\*\*\*most common cause of lower respiratory tract infx in children world wide\*\*\* leading cause of pna and bronchiolitis * S/sxs: rhinorrhea, **wheezing/coughing**, persists for months, low grade fever, nasal flaring/ retractions, often prodomal sxs for 1-2 days before **respiratory distress** * PE: visible retractions * Dx: nasal washing, **RSV antigen test** * CXR can show diffuse infiltrates * Tx: oxygen \<95-96% → hospitalize, same with tachypnea, difficulty feeding * supportive tx * should resolve in 5-7 days * albuterol via neb, humidified O2
65
Carcinoid Tumors
1-2% of lung cancers → carcinoid syndrome tumors that arise from **neuroendocrine cells** → lead to excess secretion of _serotonin_, bradykinin, and histamine * \*\*\*often start at appendix, mesastasize to liver then travel via blood stream to the **lungs**\*\*\* * S/sxs: flushing, diarrhea, wheezing, and low blood pressure * vasodilation and flushing = increased histamine and bradykinin * PE: heart valve dysfunction → tricuspid regurge due to _increased serotonin_ that causes **collagen fiber thickening, fibrosis** * Dx: **CT-scan**, **_octreoscan_** (radiolabeled somatostatin analog binds to receptors on tumor cells) * urinalysis: shows increased **5-hydroxyindoleacetic acid (5-HIAA)** = main metabolite of serotonin * **pellagra** (vitamin B3 deficiency/ niacin) * Tx: **surgical excision** * octreotide: somatostatin analog binds to somatostatin receptors and **decreases the serotonin being secreted** by the tumor * niacin supplement
66
Squamous Cell Carcinoma
non-small cell lung cancer **characterized by _keratin_ production** * S/sxs: cough, weight loss, night sweats, hemoptysis (superficial squamous cells burst in lungs), chestpain/back pain, SOB * **located in bronchial tubes (where it starts**) * paraneoplastic syndrome → **hypercalcemia** of malignancy = think stones, bones, and psychiatric overtones * → mediated by **PTHrP** (parathyroid hormone related peptide) * Tx: stage I and II: surgery * Stage IIIa: surgery +chemo * Advanced disease (IIIB and IV): * treat the driver mutation * if PDL1 is expressed by tumor → **pembrolizumab** (PDL1 inhibitor) * if PDL1 expression \<50% → **tradition chemo + PDL1 inhibitor** * _Pancoast Tumor_: should pain, horner's syndrome, brachial plexus compression * _Horner's Syndrome_: unilateral miosis, ptosis, and anhydrosis
67
Adenocarcinoma
non-small cell cancer most common type of lung cancer, and _most common type of lung cancer to occur in never smokers_ * **begins in periphery of lungs** * also associated with smoking and asbestos exposure * paraneoplastic syndrome: _thrombophlebitis_ * tx:
68
Adenocarcinoma
non-small cell cancer most common type of lung cancer, and _most common type of lung cancer to occur in never smokers_ * **begins in periphery of lungs** * PATHOLOGY: * neoplastic gland formation * also associated with smoking and asbestos exposure * paraneoplastic syndrome: _thrombophlebitis_ * tx:Tx: stage I and II: surgery * Stage IIIa: surgery +chemo * Advanced disease (IIIB and IV): * treat the driver mutation * if PDL1 is expressed by tumor → **pembrolizumab** (PDL1 inhibitor) * if PDL1 expression \<50% → **tradition chemo + PDL1 inhibitor**
69
Large Cell Carcinoma
non-small cell carcinoma very fast doubling time but causes sxs late * rare: only 5% * usually begins on the outer edges of the lungs * _paraneoplastic syndrome_: **gynecomastia** * Tx: stage I and II: surgery * Stage IIIa: surgery +chemo * Advanced disease (IIIB and IV): * treat the driver mutation * if PDL1 is expressed by tumor → **pembrolizumab** (PDL1 inhibitor) * if PDL1 expression \<50% → **tradition chemo + PDL1 inhibitor**
70
Small Cell Lung Cancer
“All of the Ss" * grow very quickly → 54-132 day doubling rate * (if faster growth than this = decreased risk of malignancy) * **aggressive and metastic** * All the Ss: * Smoking, Sentrally located, Super Aggressive, SVC syndrome, Sitting to Standing (Lambert-Eaton Myasthenic Syndrome), Sodium/SIADH→ leads to low sodium through SIADH * **TX: surgical excision is NOT an option** * _limited stage disease_ → chemo and radiation * _extensive stage disease_ → chemo + immunotherapy * _Superior Vena Cava Syndrome_: cancer pushes on superior vena cava and traps blood in upper body * _Lambert-Eaton Myasthenic Syndrome_: similar to myasthenia gravis → *proximal muscle weakness* * _Syndrome of Inappropriate Secretion of ADH_ (SIADH): * euvolemic hyponatremia → retaining too much water * _Cushing Syndrome_: too much cortisol * central obesity, purple striae, hyperglycemia * * _Carcinoid syndrome_: flushing, diarrhea, telangiectasia
71
When to Screen for Lung Cancer
pts 50-80 yo; with \>50 year pack hx of smoking, with either current smoking or having quit \<15 years ago
72
Pulmonary Nodules
nodule \<3cm (coin lesion), mass \>3cm * smooth, well defined edges → most likely benign * **ill-defined, lobular, spiculated edges** → most likely cancer * when found as incidental finding: * _Fleischner society pulmonary nodule recommendation_ * when found as part of cancer screening: * **Lung-RADS**
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Pleural Effusion
excess fluid in the pleural space * S/sxs: dyspnea, discomfort or sharp pain that worsens with inspiration * PE: _dullness to percussion_ * **decreased** tactile fremitus, **decreased** breath sounds * may have a pleural friction rub * CXR: **blunting of costophrenic angles** + _meniscus sign_ * lateral decubitus film (pt lying on their side) = best to detect smaller effusions * differentiates b/w loculations and empyema from new effusions and scarring * Tx: * **_thoracocentesis_ is both diagnostic and therapeutic** * if _empyema_ (pleural fluid pH \<7.2, glucose \<40mg/dL, or positive gram stain of pleural fluid) → can inject **streptokinase** to break up loculations * chronic effisions or recurrent and causing sxs: * **pleurodesis** (pleural space is artificially obliterated) or by intermittent drainage with an indwelling catheter
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loculations
**the compartmentalization of a fluid-filled cavity into smaller spaces** (locules) by fibrous septa
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Pneumothorax
collapse lung caused by an accumulation of air in the pleural space * **Primary**: occurs in absence of underlying disease (tall, thin males age 10-30) * **secondary**: in presence of underlying disease (COPD, asthma, CF, interstitial lung disease) * **Tension Pneumothorax**: penetrating injury → air into pleural space increased and unable to escape * S/sxs: **acute onset** ipsilateral chest pain and **dyspnea** * non-exertional, sudden * PE: decreased tactile fremitus, deviated trachea, hyperresonance, diminished breath sounds * _tension pneumo_: **mediastinal shift** to the contralateral side and impaired ventilation, **increased JVP, systemic hypotension** * Dx: * CXR: pleural air * ABG: shows hypoxemia * Tx: depends on size * \<15% (small)= will resolve **spontaneously** * **can also do high flow 100% oxygen** * \>15% (large) and symptomatic = **chest tube placement** * need to do **serial CXR every 24 hours** until resolved * _tension pneumo_: * MEDICAL EMERGENCY!!! large bore needle to allow air of the chest + chest tube for decompression * Pt Education: * avoid pressure changes 2+ weeks
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Cor Pulmonale
Right Ventricular enlargement → eventually leads to R heart failure secondary to a lung disorder that causes pulmonary HTN * Etiology: * COPD (most common), pulmonary embolism, vasculitis, asthma, ARDS * S/sxs: * worsening dyspnea, purulent sputum production, inspiratory crackles, ventricular gallop * PE: lower extremity edema, JVD distention, hepatomegaly, parasternal lift * tricuspid/pulmonic insufficiency **loud S2** * EKG: **S1Q3T3** * \*\*\*\*occurs after pulmonary HTN\*\*\*\*\* * Dx: tx the underlying condition b4 the cardiac structure change becomes irreversible * **diuretics are not helpful and MAY BE HARMFUL!**
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Pulmonary Embolism
obstruction of pulmonary blood flow due to a blood clot (usually thrombosed from a DVT) * Risk Factors: **Virchow's Triad:** 1. Damage (trauma, infx, inflammation) 2. Stasis: immobilization, surgery, prolonged sitting \> 4 hours 3. hypercoagulability: protein C or S deficiency, factor V leiden mutation, Oral contraceptive pills, malignancy, pregnancy, smoking * S/sxs: Classic Triad: * **dyspnea, pleuritic chest pain,** hemoptysis (classic but rare), cough * PE: Tachypnea (most common sign), tachycardia, low-grade fever, lung exam = normal * if large PE = syncope, hypotension, pulseless electrical activity * Dx: **helical (spiral) CT angiography** * _pulmonary angiography_ = GOLD STANDARD (may order if high suspicion and negative CT or VQ scan) * D-Dimer or ABG = respiratory alkalosis secondary to hyperventilation * _Westermark sign_: avascular markings distal to PE * _Hampton hump_: wedge-shaped infiltrate due to infarction * **atelectasis** = most common abnormal finding * Tx: **Heparin** and **oral direct thrombin inhibitors** (_dabigatran_)
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Pulmonary HTN
blood pressure in lungs is usually **very low** (15/5) pulmonary HTN → \>25mmHg usually caused by underlying disorder: constrictive pericarditis, mitral stenosis, L ventricular failure * Risk Factors: middle-aged or young women (mean age = 50), **BPMR2 gene defect** → usually inhibits pulmonary vessel smooth muscle growth and vasoconstriction * S/sxs: * dyspnea on exertion, fatigue, chest pain, edema * PE: **loud pulmonic component of S2 due to prominent P2,** may have a fixed or paradoxically split P2 * signs of R heart failure: * JVD, ascites, hepatojugular reflux * lower limb edema * pulmonary regurg, R ventricular heave, systolic ejection click * Dx: **R heart catheterization** = _GOLD STANDARD_ * CXR: enlarged pulmonary arteries, lung fields may not be clear, depends on underlying cause * **Echocardiogram**: increased pressure in pulmonary arteries, Right ventricles→ dilated pulmonary artery, dilation/hypertrophy of R atrium/ventricle * **ECG**: right heart strain pattern: T-wave inversion in R precordial leads (V1-4), and inferior leads (II, III, aVF) **cor pulmonale** * Tx: * identify and tx underlying cause * heart-lung transplant = definitive
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Idiopathic Pulmonary Fibrosis
scarring of the lungs due to unknown cause \*\*\*most common in men \>40, smokers\*\*\* * S/sxs: Worsening dyspnea, non-productive (dry) cough * PE: fine, dry, bibasilar inspiratory crackles * clubbing of fingers * Dx: * CXR: **basal predominant reticular opacities _(honeycombing)_** * Chest CT: Preferred imaging\*\*\*\* **reticular honeycombing, focal ground-glass opacifications**, bronchiectasis * PFTs: **demonstrate a restrictive pattern** (opposite of asthma) * → decreased lung volume with a normal or increased FEV1/FVC * Tx: lung transplant → only cure
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Asbestosis
lung disease caused by asbestos Occupation: insulation, demolition, construction, shipworker * S/sxs: dyspnea **on exertion**, cough * PE: bibasilar crackles * **restrictive lung pattern**: normal or increased FEV1/FVC, normal or decreased FVC, decreased lung volume (shifted to the R on loop) * Dx: * CXR: * reticular **linear pattern** with **basilar predominance, opacities**, and **honey combing** * “**shaggy heart sign**” ground glass obscures the heart * Biopsy: may show **linear asbestos bodies** * Tx: no therapy → bronchodilators, O2, corticosteroids, +/- lung transplant * \*\*\*can progress to bronchogenic carcinoma or mesothelioma\*\*\*
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Coal Worker's Pneumoconiosis
aka black lung disease occurs when coal dust is inhaled and leads to scarring in the lungs * S/sxs: dyspnea, cough, fine crackles * **caplan syndrome**: coal worker pneumoconiosis + RA (serologically positive) * PE: bibasilar crackles * **restrictive lung pattern**: normal or increased FEV1/FVC, normal or decreased FVC, decreased lung volumes * Dx: * CXR: **small nodules** especially in the **upper lung fields** with hyperinflation of the lower lobes in an obstructive pattern (looks like emphysema) * _Lung Biopsy_: show dark “black” lungs (not needed for diagnosis) * Tx: supportive care
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Silicosis
inhalation of silicone dioxide Risk factors: quarry work with **granite, slate, quartz**, pottery, sandblasting, glass, etc * s/sxs: * acute: dyspnea, cough, weight loss, fatigue * chronic: often asymptomatic, dyspnea on exertion, non-productive cough, crackles * Dx: many small (\<10mm) round nodular opacities (**miliary papttern**) mostly in the upper lobes * **_eggshell calcification_** of hilar and mediastinal nodes * bilateral nodular densities that progress * Tx: removal from exposure= MAINSTAY * nonspecific management: corticosteroids, O2, rehab
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Berylliosis
granulomatous pulmonary disease caused by exposure to beryllium used for aerospace material→ high risk: ceramics, tool and dye manufacturing, jewelry making, fluorescent light bulbs * S/sxs: dyspnea, cough, joint pain, fever weight loss * Dx: * CXR: hilar lymphadenopathy, and increased interstitial lung markings (looks like sarcoidosis) → diffuse infiltrates * tx: chronic corticosteroid use * oxygen * methotrexate if corticosteroids do not work * **associated with risk of lung, stomach, and colon cancer**
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Sarcoidosis
unknown cause, chronic multisystem inflammatory **granulomatous disease** (exaggerated T-cell response to antigens or self-antigens that leads to central immune system activation, granuloma formation, and peripheral immune depression) Risk factors: female, African American, N. Europeans, age 20-40 * S/Sxs: dry cough, dyspnea, chest pain, and crackles * affects lymph nodes as well * may have abnormal masses or nodules (granulomas) * PE: * **erythema nodosum (**classic), **lupus pernio**, maculopapular rash, anterior uveitis, restrictive cardiomyopathy, arrhythmias, heart block * Dx: serum blood tests show: **hypercalcemia** and **ACE levels x4 normal** * ESR = elevated * CXR: Bilateral hilar lymphadenopathy * _Diagnosis_: biopsy of peripheral lesion or fiber-optic bronchoscopy for central pulmonary lesion * PFTS: **restrictive pattern** * Tx: * Symptomatic pts: CORTICOSTEROIDS (1mg/kg **prednisone)** **methotrexate** and other immunosuppressive meds * **ACE inhibitors** for periodic HTN * → leading cause of death = pulmonary fibrosis
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Obstructive Sleep Apnea
intermittent obstructive airflow → results in periods of apnea at night Risk factors: OBESITY!!! structural abnormalities of the upper airway, family hx, alcohol/sedatives/opiates, hypothyroidism * S/sxs: * SNORING and **daytime sleepiness**! caused by disrupted nocturnal sleep * personality changes: poor mood and mental dysfunction * **morning headaches**, polycythemia * can lead to systemic and pulmonary HTN and **Afib** * Diagnosis: * **Polysomnography = GOLD STANDARD** * can also do home sleep apnea testing but rarely covered by insurance * _Obesity-Hypoventilation Syndrome_: -obesity (\>30BMI), -awake alveolar hypoventilation PaCO2 \>45mmHg, -alternative causes of hypercapnia and hypoventilation ruled out * Tx: * WEIGHT LOSS, exercise, avoiding alcohol/sedatives, and not sleeping supine * **oral appliances** → mild to moderate * → **BiPAP** or **CPAP** * **Uvulopalatopharyngoplasty (UPPP) →** remove extra tissue from oropharynx * **tracheostomy**
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Acute Respiratory Distress Syndrome (ARDS)
type of **respiratory failure** that is **fluid collection in the lungs** and prevents exhange of O2 * usually occurs in **critically ill** or someone with **significant injuries** * S/sxs; **rapid onset** of _sever dyspnea_ occurring 12-24 hours after a precipitating event * PE: tachycardia, **pink, frothy sputum**, diffuse crackles * Dx: sxs develop within 1 week, bilateral diffuse infiltrates on CXR (not explained by congestive heart failure) * CXR: shows **air bronchograms & bilateral fluffy infiltrate** * tx: * identify and tx underlying cause * tracheal intubation
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Influenza
ssRNA hemagluttinin and neuraminidase tx: neuraminidase inhibitors vaccines: target hemagluttinin Type A = most common Type B= humans only Type C = nonsymptomatic, little medical concern SHIFT vs DRIFT
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Histoplasmosis
* Histoplasma * S**ystemic fungi and mold → yeast at 37C** * inhalation from bats/ birds: CAVES and TREE REMOVAL * acute pneumonia sometimes developes * infect Macrophages * bone marrow disruption * apical pulmonary lesions resembling cavitary TB * tx: **itraconazole**
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Cryptococcosis
* **yeast** that can end up in the brain but is inhaled! * \*\***Defining opportunistic infection in aids patients**\*\* * skin lesions that look similar to acne, molloscum contagiosum, or basal cell carcinoma * CNS: low grade fever, ocular or facial palseys, headache * Lungs: pneumonia, AIDS (severe dyspnea) tx: **Fluconazole for non CNS, CNS: amphotericin B**
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Pneumocystis
* yeast: pneumocystis jirovecii * \*\*only issue for immunocompromised people\*\* * aerosolized: fever, dyspnea and DRY cough tx: **Bactrim (sulfamethoxazole/trimethoprim )** high risk for HIV pts with CD4 counts \<200/mcL
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Strep pneumoniae
* gram + diplococci, ENCAPSULATED * causes pneumonia: * rusty mucus * productive cough * fever * malaise * sudden onset chills and rigors (violent shaking) * causes: bacteremia and meningitis * tx: **Ceftriaxone**
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Viral PNA
most common cause in adults: **Influenza;** most common cause in children **RSV, Parainfluenza virus** * S/sxs: **persistent** sxs of sore throat, HA, myalgias, malaise for **more than 3-5 days** then **_new respiratory sxs_** _-→_ dyspnea, cyanosis * Dx: CXR: **bilateral lung involvement with interstitial infiltrate** * Rapid antigen test for influenza * _RSV_ nasal swab * _cold agglutinin titer_ to r/o Mycoplasma (should be negative with this) * Tx: flu → oseltamivir, zanamivir * RSV → **Ribavirin**
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Asthma
**reversible** chronic, inflammatory airway disease → recurrent attacks of breathlessness and wheezing that affects the trachea to the terminal bronchioles * caused by **mast cell mediators** * diminished FEV1 that is improved with inhaler * s/sxs: dyspnea, wheezing, cough, chest tightness (NOT PAIN) * worse at night * increased mucus production * PE: wheezing, prolonged expiratory phase * Diagnosis: * **GOLD STANDARD**: FEV1/FVC \< 75-80% in adults, below 85% in children * \>12% increase in FEV1 after bronchodilator * exhaled nitric oxide = can be used to measure eosinophilic airway inflammation * if pt \<5 yo = RAD, not asthma * GINA guidelines
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Cystic Fibrosis
**_Autosomal Recessive Disorder_** mutation in the CFTR gene → abnormal production of mucus by most exocrine glands → pulm infx most common cause of death (staph and HIB acute, chronic = pseudomonas) * lungs normal at birth then begin to develop pulmonary disease often during infancy or childhood * _infancy_: **meconium ileus**, failure to thrive (FTT), diarrhea from malabsorption (can lead to rectal prolapse) * _pulmonary:_: CF = **most common cause of bronchiectasis in the US** (dilation and destruction of the bronchi due to chronic infx and inflammation * PE: rhonchi and crackles * CXR may show hyperinflation, mucus pluggung and focal atelectasis * Dx: elevated sweat chloride test on **two different days** * use pilocarpine → NaCL \>60mEq/L * Tx: **CFTR genotyping** to see if they are approved for CFTR modulator therapy * hypertonic saline and chest physiotherapy → clears the secretions from the airways * tx infections * replacement of pancreatic enzymes: **supplement fat-soluble enzymes (A, D, E, K)**
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Foreign Body Aspiration
usually lodges in the larynx or trachea can lead to chronic, recurrent infx if left for a while→ PNA, ARDS, asphyxia * Risk factors: \>85 yo, \<2 yo, poor dentition, alcohol use, sedative use, institutionalization * S/sxs: Inspiratory stridor * Dx: CXR first * tx: rigid bronchoscopy = preferred for children * soft or rigid bronchoscopy for adults * surgical removal * Cxs if PNA is suspected
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Newborn Respiratory Distress Syndrome
aka Hyaline membrane disease * affects **preterm infants** when they have not produced enough **surfactant** → poor lung compliance and atelectasis * \*\*\*most common cause of respiratory distress in pre-term infants\*\*\* * Risk factors: caucasion, male, multiple births, maternal diabetes * S/sxs: * respiratory distress at birth (tachypnea \>60 /min, tachycardia, chest wall retractions, grunting, nasal flaring, cyanosis) * Dx: CXR: diffuse bilateral atelectasis that cause a **ground glass appearance** and air bronchograms * Tx: * antenatal steroids within 24-48 hours of birth → **betamethasone IM x 2** * **artificial surfactant** via ET tube * mechanical ventilation with positive pressure
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Bronchiectasis
chronic widening or enlargement of the bronchi and their branches → increased risk of infection
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Viral PNA
most common cause in adults: **Influenza;** most common cause in children **RSV, Parainfluenza virus** * S/sxs: **persistent** sxs of sore throat, HA, myalgias, malaise for **more than 3-5 days** then **_new respiratory sxs_** _-→_ dyspnea, cyanosis * Dx: CXR: **bilateral lung involvement with interstitial infiltrate** * Rapid antigen test for influenza * _RSV_ nasal swab * _cold agglutinin titer_ to r/o Mycoplasma (should be negative with this) * Tx: flu → oseltamivir, zanamivir * RSV → **Ribavirin**