RESP Flashcards

1
Q

FEV1

A

Forced expiratory volume in 1 sec

if the FEV1 is 80% or greater than the predicted value = NORMAL
Thus is the FEV1 is less than 80% of the predicted value = LOW i.e abnormal

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2
Q

FVC

A

forced vital capacity, total amount forcible expired
low fvc = airway restriction
compared with the predicted values, if the FVC is 80% or greater than the predicted value = NORMAL
Thus is the FVC is less than 80% of the predicted value = LOW i.e abnormal

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3
Q

FEV1/FVC

A

if ratio below 0.7 = airway obstruction

If the ratio is high i.e. normal but the FVC is low = airway restriction

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4
Q

RESPIRATORY FAILURE:

Types: + differences

A
  • TYPE 1 RESPIRATORY FAILURE:
    • pO2 (partial O2 pressure) is low
    • pCO2 (partial CO2 pressure) is low or normal
    • With Type 1 = 1 change = low pO2 then normal/low CO2
    • Pulmonary embolism (form of ventilation-perfusion mismatch) most commonly causes Type 1
  • TYPE 2 RESPIRATORY FAILURE: • pO2 is low
    • pCO2 is high
    • WithType2=2changes=lowpO2+highpCO2 • Hypoventilation causes Type 2
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5
Q

Restrictive vs. Obstructive Respiratory Disease: -

A

Obstructive:
• FEV1/FVC below 0.7 • FEV1 lower than FVC • ASTHMA:
- Variable airflow obstruction - Reversible
• COPD:
- Relatively fixed airflow obstruction
- May be a mixture of restrictive and obstructive disease
(• Bronchiectasis -)
Restrictive:
• FEV1/FVC above 0.7
• FVC & FEV1 below 80% predicted value
• Due to restriction, lung volumes are small and most of breath is out in first second
• Interstitial lung disease:
- FIBROSING ALVEOLITIS - SARCOID

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6
Q

COPD
Clx:
Tx:

A

Characteristic symptoms are productive cough with white or clear sputum, wheeze and breathlessness, usually following many years of a smokers cough
On examination a patient with severe disease is breathless at rest with prolonged expiration, chest expansion is poor and the lungs are hyper inflated (barrel chest)
Lung function test:
• FEV less than 80% predicted value
• FEV1/FVC less than 0.7 - airway obstruction
• Stages:
- Stage 1 - FEV1 less than 80% of predicted value - Stage 2 - FEV1 50-79%
- Stage 3 - FEV1 30-49%
- Stage 4 - FEV1 less than 30% of predicted value

Bronchodilators:
• tiotropium bromide, a long- acting antimuscarinic agent initially with a rescue short acting B2 agonist e.g. salbutamol or terbutaline to prevent /reduce acute symptoms
• A long-acting B2 agonist e.g. formoterol or salmeterol is added in patients with persistent dyspnoea (difficulty breathing)
Corticosteroids: moderate/severe COPD, a trial recommended as proportion will have a reversible element to their disease and airway function improves considerably
• Prednisolone daily for two weeks- lung function before and after treatment period
• If improvement in airflow limitation (increase in FEV by more than 15%) =discontinue prednisolone and move to inhaled corticosteroid such as beclometasone twice daily

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7
Q

ASTHMA:
Types:

Management:

A

Allergic/eosinophilic asthma (70%):
- Allergens (e.g. fungal allergens and pets etc.) & atopy
Non-allergic/non-eosinophilic (30%):
- Exercise, cold air & stress
- Smoking & non smoking associated - Obesity associated

  • Immediate management:
    • Oxygen therapy to maintain O2 sat (94%-98%)
    • Nebulised 5mg salbutamol (+ ipratropium if life threatening) - repeat/IV infusion
    • Prednisolone (with or without hydrocortisone IV)
    • Take arterial blood gases and repeat within 2 hours if severe attack
    • Chest X-ray if fails to respond to tx
    • Check PEFR within 15-30 mins/regularly
    • Oximetry to ensure SaO2 is greater than 92%
  • SABA mild
  • SABA + ICS
  • SABA + LABA + ICS
  • SABA + LABA + ICS + 4th drug e.g. anti-IgE monoclonal etc. severe
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8
Q

Bronchodilators:

Anti-inflammatory steroids:

Others:

A

• Beta2-agonists:
Short acting Beta agonist (SABA) (4 hours):
• Salbutamol (partial agonist)
• Terbutaline

Long acting Beta agonist (LABA) (12 hours):
• Salmeterol
• Formoterol (full agonist)

Muscarinic antagonists:
- Short-acting e.g. ipratropium
- Long acting e.g. tiotropium - has high affinity and disassociates
slowly from muscarinic receptors
- Act on airway M3 receptors

Methylxanthines:

  • phosphodiesterase (PDE) inhibitors: prevent conversion of cyclic-AMP to 5’-AMP = build up of cyclic-AMP and thus increased smooth muscle relaxation
  • Long-acting; theophylline (non-selective so has wide range of side effects e.g. CVS, CNS & GI tract) & aminophylline

• Inhaled corticosteroids (ICS):
- Prednisolone
• Beclomatasone
• Budesonide

-Leukotriene receptor antagonist e.g. montelukast
• Oral corticosteroid needed for those not controlled on inhaled corticosteroids e.g. prednisolone
- Steroid-sparing agents:
• Methotrexate
• Ciclosporin
• IV immunoglobulin
• Anti-IgE monoclonal antibody - omalizumab

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9
Q

HYPERSENSITIVITY PNEUMONITIS/EXTRINSIC ALLERGIC ALVEOLITIS:

Tx:

A

Chronic:

Corticosteroids e.g. prednisolone

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10
Q

BRONCHIECTASIS:
Dx:
Major pathogens on sputum culture:
Tx:

A
  • Haemophilus influenza
  • Streptococcus pneumoniae - -Staphylococcus Aureus
  • Pseudomonas aeruginosa

Antibiotics: 2 weeks
• If pseudomonas aeruginosa then high dose oral ciprofloxacin twice daily
• Haemophilus influenzae is common and responds to oral amoxicillin, co-amoxiclav or doxycycline - some multi-resistant species need IV cephalosporin
• If staphylococcus aureus then give flucloxacillin
- Bronchodilators such as nebulised salbutamol is useful for asthma or COPD
sufferers
- Anti-inflammatory agents e.g. long term azithromycin can reduce exacerbation frequency

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11
Q

CF:
Tx:

A

Prophylaxis antibiotics:
• Flucloxacillin - Staphylococcus Aureus
• Amoxycillin - Haemophilus influenzae
Pseudomonal & flu vaccine
MRSA present then treat with Rifampicin and Fucidin
Pseudomonas aeruginosa present then treat with Ciprofloxacillin and nebulised Colomycin
Regular chest physiotherapy (postural drainage, forced expiratory techniques)
B2 agonists (salbutamol) & inhaled corticosteroids (beclometasone) - purely for symptomatic relief
Mucolytics such as Dornase alfa (nebulised) or inhaled DNAse - to clear airways of mucus
Amiloride - inhibits Na+ transport thus less thick mucus Bilateral lung transplant:

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12
Q

SARCOIDOSIS:

Staging:

Tx:

A

CXR:
• Used for staging:
- Stage 0 - normal
- Stage 1 - Bilateral hilar lymphadenopathy (BHL)
- Stage 2 - Pulmonary infiltrates with BHL
- Stage 3 - Pulmonary infiltrates without BHL
- Stage 4 - Progressive pulmonary fibrosis, bulla formation (honeycombing - confluence of two or more elements of the bronchial tree) & bronchiectasis

  • Corticosteroids:
    • Prednisolone orally then gradually reduce dose • In severe illness give IV methylprednisolone
    • If steroid-resistant then:
  • Methotrexate but close monitoring required
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13
Q

IDIOPATHIC PULMONARY FIBROSIS (IPF):

RF:
Tx:

A

Risk factors:
- Factors implicated in triggering the aberrant wound healing include:
• Cigarette smoking
• Infectious agents (CMV, Hep C, EBV)
• Occupational dust exposure (metals, woods)
• Drugs - methotrexate, imipramine (anti-depressant)
• Chronic gastro-oesophageal reflux disease (GORD)
• Genetic predisposition

Pirfenidone - an antifibrotic agent that can slow the rate of FVC decline (need to check eligibility)

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14
Q

PULMONARY HYPERTENSION: def

A

defined as an mPAP of above 25mmHg as measured at right heart catheterisation and secondary right ventricular failure

Warfarin - due to intrapulmonary thrombosis

  • Diuretics for oedema
  • Oral calcium channel blockers as pulmonary vasodilators
  • Oral endothelin receptor antagonist e.g. bosenten
  • Phosphodiesterase-5 inhibitors
  • Prostanoid (mediators of vasoconstriction) analogues e.g. inhaled iloprost
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15
Q

PLEURAL EFFUSION: def

A

the excessive accumulation of fluid in the pleural space

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16
Q

BRONCHIAL CARCINOMA:
most common?

  • Non-small cell lung cancer (80% of lung cancers): Tx:
A

Adenocarcinoma - MOST COMMON OVERALL:

  • May be central or peripheral
  • Usually single lesions but they can arise in a multifocal pattern, sometimes bilaterally
  • Originate from mucus-secreting glandular cells
  • MOST COMMON CELL TYPE IN NON-SMOKERS
  • Often cause peripheral lesions on CXR/CT
  • Metastases common especially to; pleura, lymph nodes, brain, bones, adrenal glands
  • Commonly associated with asbestos

Chemotherapy +/- radiotherapy for more advanced disease e.g. with monoclonal antibodies targeting the epidermal growth factor receptor e.g. CETUXIMAB - improves mean survival

17
Q
  • WEGENER’S GRANULOMATOSIS:

Tx:

A
(Granulomatous disease of unknown aetiology)
Severe disease (biopsy proven renal disease) should be treated with corticosteroid e.g. prednisolone and cyclophosphamide or rituximab to induce remission
- Azathioprine and methotrexate are usually used as maintenance
18
Q

GOODPASTURE’S SYNDROME

TX:

A

• Corticosteroids e.g PREDNISOLONE
• Plasmapheresis (where you remove blood and clean to remove
offending antibodies before inserting it back)

19
Q

PULMONARY THROMBOLUS AND INFARCT

TX:

A

Anticoagulate with low molecular weight heparin e.g. Enoxaparin or Dalteparin

Prevention of further emboli long term:
Placed on vitamin K antagonist such as Warfarin (acts by preventing Vitamin K being used by liver to produce clotting factors 2,7,9 & 10 (1972)) - Warfarin affects the Extrinsic pathway by the Prothrombin Time (WEPT) for a period of 3-6 months
(INR 2-3)
Management of massive PE:
• Oxygen if hypoxic
• Morphine with anti-emetic if patient is in pain or very distressed

20
Q

SINUSITIS:
TX:

A

(Infection of the paranasal sinuses that is bacterial or occasionally fungal)

  • Nasal decongestants such as xylometazoline
  • Broad spectrum antibiotics such as co-amoxiclav (H.influenzae can be resistant to amoxicillin)
21
Q

ACUTE EPIGLOTITIS:

TX:

A
  • IV antibiotics e.g. ceftazidime
22
Q

WHOOPING COUGH - BORDATELLA PERTUSSIS:

TX:

A

Antimicrobials such as macrolides e.g. clarithromycin will eliminate carriage of bacteria and reduce symptoms in catarrhal stage and early paroxysmal stage

23
Q

CROUP/ACUTE LARYNGOTRACHEOBRONCHITIS:

TX:

A

Oral or intramuscular corticosteroids e.g. dexamethasone should be given with oxygen and adequate fluids

24
Q

LOWER RESPIRATORY TRACT INFECTIONS: - PNEUMONIA EXPLAINED

A

Defined as inflammation of the substance of the lungs
An acute lower respiratory tract infection
Usually caused by bacteria but can also be caused by viruses and fungi
Usually due to infection affecting distal airways and alveoli with the formation of an inflammatory exudate

25
Q

HAP is the

which pathogens

A

second most common form of hospital acquired infection after UTI’s

Aerobic GRAM-NEGATIVE bacilli/rods are MOST COMMONLY involved:

  • Pseudomonas Aeruginosa - Escherichia coli (E.coli)
  • Klebsiella Pneumoniae
26
Q

Organism indicated in CAP:

A
• Streptococcus pneumoniae (most common) 
• Haemophilus influenzae
• Atypical:
- Mycoplasma pneumoniae
- Chlamydophila pneumoniae
• Enteric GRAM-NEGATIVE BACTERIA:
- E.coli
- Klebsiella pneumoniae
27
Q

Organisms indicated in HAP:

A

• GRAM-NEGATIVE BACTERIA:
- Pseudomonas aeruginosa - E.coli
- Klebsiella pneumoniae
• Staphylococcus Aureus including MRSA

28
Q

Pnemonia:
Tx:

A

Analgesia such as paracetamol or NSAID : pleuritic pain - reducing risk due to restricted breathing e.g. sputum retention or secondary infection
Narrow spectrum antimicrobials if mild = amoxicillin 5-7days
IV antibiotics if severe = co-amoxiclav or clarithromycin 7-10 days

Special cases: Severe Legionella spp. pneumonia:
- Ensure fluoroquinolone in regimen either alone or with clarithromycin
Necrotising pneumonia or other features of Panton-Valentine leukocidin (PVL - a cytotoxin prodcued by some aggressive strains of S.aureus that causes a necrotising pneumonia) producing S.aureus infection:
- IV linezolid
- IV clindamycin
- IV rifampicin

Pseudomonas aeruginosa:

  • IV ceftazidime
  • With gentamicin/tobramycin
29
Q

Pneumonia complications:

Tx of them:

A

Respiratory failure
Hypotension - due to a combination of dehydration and vasodilation due to sepsis
Parapneumonic effusion & empyema:

Antimicrobials:

  • Co-amoxiclav
  • Piperacillin-tazobactam
  • Meropenam (for anaerobic coverage)
30
Q

TUBERCULOSIS: micro?

Systemic features:

Tx:

A

Acid-fast bacilli (resist decolorisation) - go red/pink with Ziehl-neelsen stain

• Weight loss (most predictive of TB)
• Low grade fever
• Anorexia
• Night sweats (most predictive of TB)
• Malaise
CONSIDER TB FOR ANY CHRONIC ILLNESS WITH FEVER & WEIGHT LOSS!!!!
ALL CASES OF TB MUST BE NOTIFIED TO PUBLIC HEALTH ENGLAND

Patients with fully sensitive TB require 6 months of treatment (in CNS TB need 12 months):
• Rifampicin for 6 months:
- Bactericidal, blocks protein synthesis - effective throughout treatment course
• Isoniazid for 6 months:
- Bactericidal for rapidly growing bacilli (blocks cell wall
synthesis), most effective in initial stages
• Pyrazinamide for first 2 months:
- Bactericidal initially, less effective later
• Ethambutol for first 2 months:
- Bacteriostatic, blocks cell wall synthesis -
• Remember by “RIPE”