COPD and Bronchiectasis Flashcards

1
Q

preventable and treatable disease, is characterized by persistent respiratory symptoms and airflow limittaion that is due to airway and/or alveolar abnormalities caused by significant exposure to noxiuos particles or gases

A

COPD

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2
Q

Most common respiratory symptoms of COPD

A

Dyspnea
cough
sputum production

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3
Q

Most important risk factor in COPD

A

Cigarette smoke

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4
Q

key cell playes in COPD

A

Neutrophils, macrophages and CD8

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5
Q

Pathogenesis of COPD

A

Plasma leakage, sensory nerve impairment, smooth muscle constriction

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6
Q

____is already present in the early stages of COPD

A

Inflammation

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7
Q

Gold stage 0

A

asymptomatic but smoking individual

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8
Q

Airway inflammation is characterized by

A

Increased numbers of neutrophils, macrophages and CD8 lymphocytes

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9
Q

Effect of COPD in bronchus

A

Wall thickening and inflmmation -> mucus gland hypertrophy -> increased secretions -> phlegm

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10
Q

Effect of COPD in bronchiole

A

Wall thickening->inflam_>repair->remodeling->loss of alveolar attachment

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11
Q

Effect of COPD in alveoli

A

Wall thinning ->inflammation ->elastolysis coalescence ->decreased elasticity

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12
Q

In asthma the basement membrane

A

Thicken because smooth muscles are hyper reacting

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13
Q

Mediators in asthma

A

IL-4 IL5

LTD4, histamine, ROS

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14
Q

Mediators in COPD

A

IL-8 and TNF alpha

LTB4, ROS

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15
Q

Effects in asthma are in the___

A

All airways

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16
Q

Effects in COPD are in the _____

A

Peripheral airways

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17
Q

Mechanisms underlying airflow imitation in COPD

A

Small airway disease

PArenchymal destruction

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18
Q

Cause of airflow limitation

A

Irreversible, Fibrosis and narrowing of airways

Loss of elastic recoil due to alveolar destruction

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19
Q

Primary site of airflow limitation:

A

Peripheral airways (bronchi and nronchioles <2mm)

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20
Q

PFT results in COPD

A

FRC increases
RV increases to detriment of inspiratory capacity decreases
TLC and TV stays the same

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21
Q

Pathophysiological Changes in COPD

A
Mucus hypersecretion
Ciliary dysfunction
Airflow limitation
Pulmonary hyperinflation
Gas exchange abnormalities
Pulmonary hypertension
cor pulmonale - leads to death
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22
Q

total volume of air expired after a full inspiration

A

Fore vital capcity

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23
Q

volume of air expired in the first second during maximal respiratory effort

A

FEV1

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24
Q

Goal of COPD Assessment

A

To determine level of airflow limitation, its impact to patient’s health status and the risk of future events to eventually guide therapy

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25
Classification of severity of airflow limitation in COPD:
GOLD 1: mild FEV1/FV <0.70 GOLD 2: Moderate; 50%
26
Tools for assessment in COPD
mMRC breathlessness scale COPD assessment Test (CAT) Clinical COPD questionnaire
27
Modified MRC Questionnaire
Assesses patient's level of breathlessness or dyspnea at various activities
28
COPD Assessment Test
8 item questionnaire Scoring system : 0 to 40 If score is at least 10-more = symptomatic
29
Assess Risk of exacerbation
Ask history: >2 in the past year FEV1 postBD <50% predicted >1 hospitalization for COPD in the past year
30
Performed when COPD develops in patient of caucasian descent >45 years or with a strong family history COPD
Alpha-1 Antitrypsin Deficient Screening
31
Characterized by persistent airflow limitation with several features usually associated with asthma and COPD
Asthma-COPD Overlap syndrome
32
How to manage ACOS
treat asthma first, then COPD
33
Goals of therapy in COPD
Reduce symptoms Reduce risk Avoidance of risk factors through:
34
Greatest capacity to influence the natural history of COPD
Smoking cessation
35
Brief strategies to help the patient willing to quit smoking
``` ASK ADVICE ASSESS ASSIST ARRANGE ```
36
Stimulate beta-2 receptors, thus relax airway smooth muscle
Beta-2 agonist
37
Block the effect if Ach on M3 receptors and relax smooth muscle
Anti-cholinergics
38
Exact MOA controversial; Antagonize bronchoconstriction through PDE4 inhibition in smooth muscle;
Methylxanthines
39
Eacerbations are reduced by ______in patients with severe and very severe COPD (GOLD 3 and 4) and a history of exacerbations
ROFLUMILAST (PDE4) inhibitors
40
Management of Group A
Give bronchodilator->Evaluate effect _> change if ineffective
41
management of group B
Mandatory put in LAMA or LABA depending on patient and behavior on side effect
42
management of Group C
LAMA, if with exacerbations, shift to LAMA +LABA Alternatively LAMA +ICS
43
management of Groupd D
Dual therapy (LAMA+LABA) If with exacerbations, sequentially add: ICS, PDE4, Macrolide, Descalation of symptoms
44
Pneumococcal polysaccharide vaccine is recommended for those who are
65 years old and older | Younger than 65 with FEV1 <40% predicted
45
Removal of hyperinflated section
Lung volume Reduction Surgery
46
an acute event characterized by worsening of the patient's respiratory symptoms that is beyond normal day to day variation and leads to a change in medication
Exacerbations
47
Most common cause of COPD exacerbation
Viral infection
48
Antonisen Criteria
At least two of the following cardinal symptoms: Shortness of breath Sputum purulence Increase sputum volume ``` or any one of the above plus URTI Wheeze Cough Increased PR/RR ```
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Mild Exacerbations
Requiring more reliever medication
50
Moderate Exacerbations
Systained worsening symptoms (2-3 days) Need for antibiotic and or systemic CS Unscheduled hospital visits
51
Severe Exacerbations
Require hospitallization
52
Oxygen saturation
88-92%
53
Antibiotics should be given to patients with
Increased dyspnea, sputum volume, and sputum purulence
54
Abnormal and permanent dilatation of the medium-sized bronchi , destruction of elastic and muscular components of their walls, primarily mediated by neutrophils
Bronchiectasis
55
Primary criteria for bronchiectasis
Impairment of mucociliary drainage in one or both of the lungs. - Acute or chronic infection - Anatomic airway obstruction - Congenital disease that predisposes to chronic infection
56
enzyme deficiency that produce non-functional cilia
Alpha-1 anti trypsin deficiency
57
SIte of pathology in bronchiectasis
Medium sized bronchi - replaced by fibrous tissue
58
Causes of bronchiectasis
``` Post infective Mechanical obstruction Deficient immune response Inflammatory pneumonitis Congenital Excessive immune response Abnormal mucus clearance Fibrosis ```
59
reed classification
Radiologic classification
60
Reed classification (Radiologic)
Cylindrical Bronchiectasis -Sections of bronchi are consistently widened Varicose Bronhiectasis - There are local constrictions and there is an irregular pattern that closely mimics that of the varicose veins Saccular (Cystic) Bronchiectais - dilation increases towards the peripheral areas of the lung; honeycombing
61
Predominant organism in sputum of bronhiectasis patient
gram negative
62
Cystic fibrosis
Mucoviscoidosis AR disorder CFTR protein
63
Cystic fibrosis Diagnosis
Gibson-Cooke Sweat Test -Gold standard -Forearm sweat stimulated with pilocarpine (+) >60mml/L Cl
64
Clinical features of Cystic fibrosis
Coughing, dyspnea, and expiration of foul, voluminous secretions especially prevalent in the morning
65
Signet ring sign on Chest CT
bronchiectasis
66
Only curative treatment of bronhiectasis
Surgical Treatment