Clinical Flashcards

1
Q

What’s the most common presentation for restrictive lung disease?

A

cough

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2
Q

What test should you use to distinguish between restrictive and obstructive lung disease? what finding would indicate these diseases?

A

spirometry

Low FEV1/FVC obstructive. TLC normal or increased

normal or high FEV1/FVC restrictive. TLC decreased

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3
Q

How would you asses the severity of a restrictive lung disease? How do you interpret your findings?

A

DLCO- diffusion capacity and lung volumes

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4
Q

What tests would you use to differentiate between types of restrictive lung disease?

A

DLCO, CXR, and lab tests

Decrease DLCO indicates a interstitial or infiltrative lung disease

Normal DLCO suggests Non pulmonary cause: neuro or MSK

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5
Q

What are some useful values to know when you suspect a neuromuscular cause for a restrictive lung disease? What do you do if this is confirmed?

A

MIP maximal inspiratory pressure
MEP maximal expratory pressure

abnormal in suspected neuromuscular disease like ALS

patient will likely present with other neurologic complains including weakness and fatigue.

Refer to neurologist

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6
Q

Your patient has an increased FEV1/FVC and decreased TLC. DLCO is also decreased. What test would be most appropriate to do first at this point?

Bronchoalveolar lavage
100% O2 15 mins
Spirometry
CXR

A

Bronchoalveolar lavage to distinguish the type of interstitial lung disease (ILD)

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7
Q

You have a patient with chronic dyspnea that you suspect of having a restrictive lung disease. What other PE findings might be present? What’s one confounding factor to this diagnosis should it be present?

A

Check for crackles, cyanosis and additional signs (other than ascities) of R heart failure; JVD ect.

chest pain would be confounding and may relate to systemic disease such as lupus, RA, or sarcoidosis.

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8
Q

What are some signs of interstitial lung disease (ILD) or diffuse parenchymal lung disease (DPLD)? Extrinsic disorders? Neuromuscular?

A

ILD, DPLD- inflammation and scarring of lung tissue on CXR

Extrinsic disorders- disorders that limit expansion of the lungs; chest wall or pleura. (scoliosis or obesity)

Neuromuscular disorders: decrease ability of respiratory muscles to inflate and deflate the lungs.

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9
Q

Discuss the cough reflex: receptor location, nerve involvement and primary brain center involved

A

Receptor locations-pharynx, larynx and tracheobronchial tree esp carina

Vagus nerve

Medulla

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10
Q

Describe the 3 phases of a cough

A
  1. Inspiratory-air in lungs
  2. Compressive-Glottis closes to build intrathoracic pressure from expiratory muscle contraction
  3. Expiratory- release of air (50-500mph)
  4. Recovery breath.
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11
Q

Discuss the causes and consequences of an ineffective cough

A

Cause
Intrinsic pulmonary diseasese-obstructive and restrictive. Impairment of expiratory flow or excessive secretions

Extrapulmonary disorders-CNS, PNS, chest wall or upper airway conditions

Consequence
Ineffective clearance of airway
Retained secretions
Atelectasis or infections; the latter can lead to bronchiectasis (permanently dilated airways)

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12
Q

What are 10 complications of a cough

A
  1. cardiac arrhythmias (vagas nerve involvement)
  2. syncope (vaso-vagal)
  3. Herniations
  4. urinary incontinence (pregnant women)
  5. Rib fracture
  6. headaches
  7. Pneumothorax
  8. Ruptured blood vessels
  9. Decreased quality of life
  10. laryngeal trauma (hoarseness)
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13
Q

How are coughs classified

A

Acute less than 3 wks
Subacute 3-8wks
Chronic 8 + wks

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14
Q

Compare and contrast hx and PE findings for acute cough

UACS
LRI
COPD
Aspiration 
Pul embolism
CHF
A
  1. Upper airway cough syndrom (UACS)

Common etiologies

a. URI- usually viral, post nasal drainage, tubinate erythema.
b. Acute bacterial sinusitis- purulent nasal drainage, headaches, may start as URI (similar)
c. Allergic rhinitis-rhinorrhea, sneezing, congestion, no fever. Pale turbinates

  1. Lower respiratory infection
    Adventitious lung sounds, usually viral- pertussis, pneumonia.
  2. COPD-cough changes
  3. Aspiration- Sudden chocking and coughing- young and very old. unilateral decreased breathing sounds
  4. Pulmonary embolism- Risk factors: DVT, surgery. Symptoms-chest pain, dyspnea, tachypnea, tachycardia.
  5. CHF- Pulmonary congestion
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15
Q

Know the alarm systems for cough related to a potentially life threatening cause

A
  1. Hemoptysis- Serious cause: lung cancer, TB, Pul embolism, Pneumonia. Benign: acute bronchitis
  2. Fever, purulent sputum- Serious cause: Pneumonia, lung absecss. Benign- sinusitis
  3. Wheezing and SOB- Serious: Asthma, COPD, CHF. Benign: Acute Bronchitis
  4. Chest pain- Serious: acute coronary syndrome, Pul. embolism. Benign: Pleurisy
  5. Dyspnea and edema: Serious: Pul. embolism, CHF. no benign
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16
Q

What’s the diagnostic approach to a patient with chronic cough. What investigative studies are useful

A

Treat symptoms, if ineffective try potential irritants (smoking, ACEI ect) if inneffective look into top 3 causes and treat in turn; any therapy that works you maintain.

Treatment:
UACS- antihistamine, decongestant
Asthma- albuterol, corticosteroids, methcholine challenge
GERD- elevate bed, lose weight, PPI or H2 blocker

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17
Q

Describe the pathophysiology of non-pulmonary cough

A

Cardiac
GERD-reflex stimulation more than acid as trigger. Suggestive findings dys____everything: taste, swallowing horse voice, acid reflux. May take 3 months to treat.

Swallowing disorders-stroke lead to aspiration pneumonia and death, neuromuscular disorders ALS etc

Congenital- Tracheo-esophageal fistula lead to severe or fatal complications due to aspiration: Trachea attached to side of the esophagus, or the esophagus branching out from the trachea.

Psychogenic- tic

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18
Q

OMT treatment for various cough etiologies

A

No thoracic pump release with COPD dont rupture a bleb.

Treat- anterior cervical fascia, cervical ME or HVLA, thoracic HVLA.

19
Q

Which common drug can cause a chronic cough?

A

ACEI. switch to ARB

20
Q

What time of day is a smokers cough the worst and why?

A

First thing in the morning, because the cillia are getting active again and making mucous.

21
Q

How might you do a simple test to tease out an upper vs lower respiratory tract disorder?

A

Have the person cough as a test to see if they clear out any obstruction, if it persists it maybe URT disorder.
LRT may present with rales or rhonchi.

22
Q

What are the three most common causes of chronic cough?

A

UACS, Asthma, GERD 90%

If non-smoker, with no ACEI, and normal CXR 99% likely

25% multiple causes

23
Q

Cite differences between pediatric and adult airways

A

More acute angle of the epiglottis
Larger tongue
Angled vocal cords
Funnel shaped larynx -narrows to the cricoid cartilage

24
Q

List signs of a child in respiratory distress compared to normal

A

Distress: use of accessory muscles to breath

Respiratory observations-retraction of chest, nasal flare, tracheal tug, leaning forward, irritability, decreased responsiveness

Increased respiratory rate

Auditory breath changes- grunting, wheezing

25
Q

Describe signs of clinical respiratory failure

A

A child that is unable to maintain adequate O2 despite extra effort and breathing rate.

26
Q

What are some respiratory causes of dyspnea that would be considered obstructive airway problems?

A
Choanal atresia
retropharyngeal abscess
papillomas
Inflammation/Infection
Epiglottitis
Croup
Foreign body aspiration
27
Q

Describe epiglottitis

A

Sudden onset: Life-threatening bacterial infection of the epiglottis
Haemophilus influenza B (Hib)

Swollen epiglottis and aryepiglottic folds
CT-thumbs up sign, or endoscopy see cherry

4Ds
dysphagia, dysphonia (Hot potato voice), drooling, distress

Don’t look at it the airway may occlude.

28
Q

What are the signs and symptoms of foreign body in the airway

A
Ball valve (one way valve, easy to breath in, not out)
Acute respiratory failure
Cyanosis
Cough, gagg
Stridor
Wheeze

Sudden onset

29
Q

What’s a TEF?

A

Tracheoesophageal fistula- This is when the esophagus is malformed and can attach to the trachea in various ways. This can lead to aspiration and breathing complications

30
Q

What’s a diaphragmatic hernia?

A

When hole in diaphragm that allows the abdominal contents to move into the chest cavity.

31
Q

What are some characteristic findings for croup on X-ray?

A

Steeple sign. Caused by inflammation of area around the vocal cords and trachea

32
Q

Which complication of pierre robin sequence is typical of infant airway obstruction?

A

Tongue falls back against the posterior pharynx and causes airway obstruction

33
Q

The obstruction of which airway is especially serious in infants less than 2 months; why? Name a condition in which bone obstructs this airway.

A

These infants are obligate nose breathers

Choanal atresia is complete nasal obstruction of a newborn due to bony obstruction. This can lead to infant death by asphyxia

34
Q

How is hemoptysis different from hematemesis?

A

Hemoptysis-

cough
no nausea or vomiting
frothy sputum
blood tinged sputum persists for days
hx lung disease 
Significant blood loss uncommon
asphyxia possible 

Hematemesis (opposite)
no cough etc.
hx gastric or liver disease.

35
Q

What are some common etiologies of hemoptysis in order of frequency of occurrence?

A
Bronchitis
Lung cancer
Bronchiectasis
Cryptogenic
Pneumonia
TB
36
Q

What are some cardiovascular disorders related to hemoptysis; characterize them

A

Mitral valve stenosis (Rheumatic fever), or L ventricular failure- pink frothy sputum

37
Q

Describe in general terms the respiratory pathogenesis of hemoptysis

A

Frequently involves abnormal vasculature at risk of injury: vasculitis, infection, inflammation, malignancies, AVM, crack cocaine use, pulmonary edema (vascular injury and release of RBC; pink frothy sputum) .

If TB cavitary leson erodes blood vessel you can have massive hemoptysis

If pulmonary embolism leads to infarction=dark red hemoptysis.

38
Q

What are some traceobronchial causes of hemoptysis?

A

Bronchitis
Bronchiectasis
Bronchogenic carcinoma

39
Q

What are some pulmonary parenchyma causes of hemoptysis?

A

TB, Pneumonia, vasculitits, fungal, abscess,

40
Q

What are some primary vascular causes of hemoptysis?

A

Pulmonary embolism-DVT leading to infarct; dark red sputum. pleural effusion and atelectasis. CTA good test.

Crack cocaine-injury to alveolar capillary membrane

Cryptogenic-diagnosis of exclusion. 90% fine in 6 months.

Meds-anti-coagulants, aspirin, cocaine, NSAIDS,

41
Q

Classify hemoptysis

A

mild specks of blood in sputum
moderate specks to 200ml in 24 hrs
massive greater than 200ml

42
Q

What labs or procedures are common when investigating hemoptysis?

A

CXR

CBC w/diff-infections

ESR-infection, autoimmune

HRCT for suspected bronchiectasis

Bronchoscopy with washing for cytology and C&S for suspected: Brochogenic carcinoma

Pulmonary embolus- CT angiography, D-dimer

TB- TST skin test

Biopsy tumors to determine if they’re benign, and to differentiate between small cell and non small cell carcinoma (so you know if chemo is better than surgery)

43
Q

Massive hemoptysis can lead to what fatal complication? How can you prevent it?

A

asphyxiation and respiratory arrest due to blood flooding the tracheobronchial tree.