Respiratory Flashcards

1
Q

Chlamydia Psittaci

  1. Treatment (1st Line and 2nd Line)
  2. How does it Present ?
A

1st Line = Doxycycline
2nd Line = Macrolides

Severe Pneumonia + Headaches + Organomegaly + Failure to respond to PENICILLIN base Antibiotics

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2
Q

Cystic Fibrosis Gene and Mutation

A

Delta F508 Deletion in Long Arm of Chromosome 7

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3
Q

Organisms that Colonize Cystic Fibrosis Patients ?

A
  1. Staphylococcus Aureus
  2. Pseudomonas Aeruginosa
  3. Burkholderia cepacia
  4. Aspergillus
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4
Q
A

pH<7.2 - Indication for placement of chest tube in Pleural Effusion.

PH <7.35 - Indication for ventilation and intubation in Asthma.

PO2<7.3 - Indication for LTOT.

FEV1 <1.5 - Contraindication for lung cancer resection

PaO₂ < 9.3 kPa in PCP - add corticosteroids in Tx.

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5
Q

Cystic Fibrosis Treatment

A
  1. Chest Physio
  2. High Fat diet
  3. Minimize Contact with other CF patients
  4. Creon
  5. Lumacaftor (More CFTR) /Ivacaftor (Potentiate existing CFTR) (Orkambi)
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6
Q

Contraindication for Lung Transplant in Cystic Fibrosis

A

Burkholderia cepacia

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7
Q

What type of Ventilation in :

COPD with Acidosis ?
T1RF
T2RF

A

NIV
CPAP
BiPAP

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8
Q

Allergic BronchoPulmonary Aspergillosis

  1. Treatment
  2. Features
A
  1. Corticosteroids
  2. Raised IgE + Eosinophilia + Positive IgG precipitins
    (NOT as positive as in aspergilloma)

Recurrent Chest Infections and NOT RESPONDING TO ASTHMA TREATMENT

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9
Q

What is the X ray finding for ABPA ?

A

Fitting CXR - transient migratory pulmonary infiltrates

PROXIMAL Bronchiectasis

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10
Q

Panacinar vs Centri acinar in COPD
Aetiology

A

Centri-Acinar in Smokers and Coal Worker Pneumoconiosis

Panacinar - Alpha-1- Antitrypsin Deficiency

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11
Q

Causes of Bronchiectasis

A

‘A SICK AIRWAY’

Airway obstruction/ lesion

Sequestration

Infection/Inflammation

Cystic Fibrosis

Kartagener’ s Syndrome

ABPA

Immunodeficiencies(Hypogammaglobinemia,Myeloma,
Selective igA deficiency,Lymphoma )

William Campbell Syndrome

Aspiration

Yellow Nail Syndrome/Young Syndrome

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12
Q

Tram Track Sign on X ray defined as ?

A

Dilated Bronchi with Thickened Walls in the Lower Zone

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13
Q

Common Organism to colonize in CF

A

Psuedomonas in ADULTS
S.Aureus in CHILDREN

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14
Q

Most Common Organisms Colonizing Bronchiectasis patients

A
  1. Haemophilus influenzae
  2. Pseudomonas aeruginosa (Long History and PPI Use associated)
  3. Klebsiella spp.
  4. Streptococcus pneumoniae
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15
Q

Mnemonic for Upper Lobe Fibrosis

A

A TEA SHOP

ABPA

TB
Extrinsic Alveolar Alveolitis
AS

Sarcoidosis
Histiocytosis
Occupational (Silicosis and Berylliosis)
Coal Worker Pneumoconeosis

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16
Q

Mnemonic for Lower Lobe Fibrosis

A

IPAS-BM

Infection

A
Aspiration
Alpha 1 Antitrypsin
Asbestosis

S
Systemic Sclerosis
RA

Bronchiectasis

Medications - Busulfan Bleomycin Nitrofurantoin Hydralazine Methotrexate Amiodarone

or SCAR

Systemic Sclerosis
Cryptogenic Fibrosing Alveolitis (IPF)
Asbestosis
RA

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17
Q

Smoking Cessation

A

Varenicline - a nicotinic receptor partial agonist
Start 1 week before Target Stop Date

Start 1 week before Target to Stop Date and 12 weeks course (Only continued if stop attempted)

SELF HARM or SUICIDAL BEHAVIOR CONTRAINDICATED

Bupropion -
norepinephrine-dopamine reuptake inhibitor and nicotinic antagonist

Start 1 to 2 weeks before Target Stop Date

Seizures Risk –> CONTRAINDICATED IN EPILEPSY

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18
Q

Smoking Cessation in Pregnancy

A

Varenicline and Bupropion CONTRAINDICATED

Give CBT and Motivational Interviewing

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19
Q

Meigs Syndrome Triad ?

A

Ascites + Pleural Effusion, + Benign Ovarian Tumor

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20
Q

Right Sided Pleural Pneumothorax + Menstruating Women Think What ?

A

Catamenial Pneumothorax

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21
Q

Mnemonic for Pleural Cavities

A

CAVITY

Cancer - Lung SCC

Autoimmune -
RA , Wagener’s Granulomatosis

Vascular - Bland and Septic Emboli

Infection - PTB, Pulmonary Abscess

Trauma - Pneumatocele

Youth -
Congenital Airway Malformations
Bronchogenic Cysts

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22
Q

Red Flags for Chest Drain insertion ?

A

Hemodynamic Compromise

Severe Hypoxia

Bilateral Pneumothorax

Underlying Lung Disease

> /50 with Significant Smoking History

Hemopneumothorax

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23
Q

Discharge Advice for Patients treated for Pneumothorax

A

Scuba Diving - NEVER unless B/L Pleurectomy + Normal CT and PFT

Flying - 1 week post check X ray

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24
Q

LTOT offered in COPD if ?

A

2 ABG showing PO2<7.3
3 weeks apart

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25
Q

What type of Lung Cancer is Associated with Non Smokers ?

A

Adeno Carcinoma

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26
Q

Difference between Biopsy for EAA vs Sarcoidosis

A

EAA - Non Caseating Granuloma BUT LESS DENSE AND LESS DEFINED

Sarcoidosis - Non Caseating Granuloma BUT MORE DENSE AND DEFINED

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27
Q

EAA

  1. Pathophysiology
  2. Radiological Findings
  3. Clinical Progression
  4. Treatment
A
  1. Not IgE associated
    Not Eosinophilia Associated
    No Type 1 HSN

Acute (Type 3) and Chronic (Type 4) vs ABPA (TYPE 2)

  1. Upper / Middle Lobe Fibrosis
    Honey Combing
    Ground Glass
  2. Fibrosis then Respiratory Failure then Hypoxemia
  3. Avoidance
    Oral Glucocorticoids
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28
Q

Byssinosis
What exposure ?

A

Cotton / Flax / Textile

Monday Chest Tightness

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29
Q

Silo Fillers Lung
What Exposure ?

A

Nitric Oxide from Grain Dust in Silos

Type 1 HSN so Not EAA

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30
Q

When to give steroids in Sarcoidosis

A

Symptomatic + Stage II/III
Hypercalcemia
Ocular Neuro or Cardiac Involvement

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31
Q

In EAA Farmers Lung makes you have Emphysema (Obstructive Picture) but Bird Farmers Lung causes Fibrosis (Restrictive Picture)

A

So in EAA both Restrictive and Obstructive Picture can be seen

REMEMBER THIS

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32
Q

Pleural Plaques in Asbestosis are BENIGN

They increase risk of Pleural Effusion NOT MESOTHELIOMA

A

Remember this point

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33
Q

Inspiratory Capacity = ?

Functional Residual Capacity = ?

Residual Volume = ?

Expiratory Reserve Volume (ERV) Reduced by What ?

Vital Capacity = ?

Total Lung Capacity = ?

A

Tidal Volume + Inpiratory Reserve Volume

Expiratory Reserve Volume + Residual Volume

FRC - ERV

Obesity

Inspiratory Capacity + ERV

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34
Q

Treatment for IPF

A

Pulmonary Rehabilitation
Breathless on Exertion –> LTOT
Vaccinate Pneumococcus and Influenza

If FVC<50-80% = Antifibrinolytics

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35
Q

Radiological Findings

A

Stage 1: Lower zone lung opacification

Stage 2: Ground glass

Stage 3: Honeycomb

36
Q

Causes of Exudative vs Transudative Pleural Effusion ?

A

Exudative

Malignancy
Pneumonia and Parapneumonic Effusions
Pancreatitis
Autoimmune ( RA Churgg Straus Pleurisy)
Post MI

Transudative

CHF Cirrhosis Nephrotic Syndrome
Peritoneal Dialysis
PE
Hypothyroidism

37
Q

Lights Criteria

A

Exudative if 1 of

Pleural LDH/ Serum LDH >0.6

Pleural Protein/Serum Protein >0.5

Pleural LDH >2/3rd upper limit of Serum LDH

38
Q

Why does HAPE and HACE occur ?

A

HAPE - High Altitude Pulmonary Edema

Uneven Pulmonary Vasoconstriction from Hypobaric Hypoxia

HACE - High Altitude Cerebral Vasodilation

39
Q

Treatment for HACE and HAPE

A

HAPE

Descent and Oxygen
Nifedipine , Dexamethasone, Acetazolamide
PDE5i

HACE

Descent
Dexamethasone

40
Q

Acute Mountain Sickness Preventative and Treatment

A

Acetazolamide -

Preventative by creating a primary metabolic acidosis and compensatory respiratory alkalosis –> improving RR

Treatment is DESCENT

41
Q

Where is NIV not indicated ?

A

Bronchiectasis (a Trial only at best)
Limited by excessive secretions

42
Q

Oxygen Dissociation Curve Mnemonic ?

A

Left Shift - We have LEFT the tissue behind (Cells hold onto Hb)

Right Shift - Giving Oxygen to Tissues

43
Q

Causes of Right and Left Shift in Oxygen Dissociation Curve

A

Right Shift (CADET)

Raised PCO2
Raised Acid
Raised 2,3-DPG
Raised Temperature

Left Shift

Low (ABOVE 5)
Hb F
Met Hb
Carboxyhemoglobin

44
Q

Examples of Hemoglobin Structural Changes that make LEFT SHIFT

A

Changes to Heme Affinity -
Hb Kempsey (β99 Asp→Asn) - INCREASED O2 Affinity

Changes to Allosteric Regulators like 2,3-DPG
- Hb Rainier (β145 Tyr→His) - INCREASED O2 Affinity by making Hb more sensitive to regulators

HbS (Valine to Glutamate at C6)

45
Q

Causes of Respiratory Alkalosis

A

Hyperventilation
PE (+ REDUCED PaO2)
Altitude
Pregnancy
CNS - Stoke Encephalitis SAH
Salicylate Poisoning (Early Resp alkalosis –> Metabolic Acidosis)

46
Q

What causes a Raised TLCO ?
Watch Medicosis Video)

A

PELHAM for raised TLCO

P ulmonary haemorrhage, polycythaemia
E xercise
L eft to Right shunts
H yperkinetic states
A sthma (Late Stage Neovascularization)
M ale gender

Reduced DLCO

Reduced Perfusion

Systolic HF
Anaemia
Pulmonary Embolism
PAH (Narrowed)
Systemic Sclerosis (Damage to Pulmonary Artery)
ASBESTOSIS

Decreased Perfusion

INTRINSIC Restrictive Lung Disease
Medications
Emphysema

47
Q

Dyspnea + Obstructive Pattern + RA = >

A

Bronchiolitis Obliterans

48
Q

How does Bronchiolitis Obliterans Appear on CT

A

Centrilobular Nodules with Bronchial wall Thickening

49
Q

Conditions with Raised KCO ?

A

KCO = TLCO / VA

VA roughly is lung volume or effective lung volume in compared to normal healthy lungs)

So Raised KCO means ether TLCO is increased or VA is reduced.

In here, Raised KCO is pretty much poor lung volume (Low VA)

ANK SPOND, Scoliosis, kyphosis = lung posture

NM weakness (Also reduced effective lung volume)

Lobectomy and pneumonectomy (again low lung volume).

*TLCO also known as DLCO on the web.
*KCO = DLCO/VA
*VA = effective lung volume

50
Q

ERV is low in which patients and why ?

A

Obese because of decreased chest wall compliance

51
Q

OSA Treatment ?

A

Weight Loss
CPAP
If not tolerated Oral mandibular devices

52
Q

OSA Acid Base Picture ?

A

Compensated Respiratory Acidosis

53
Q

LTRA Side Effects ?

A

Unmasking Churgg Strauss Syndrome

Hepatic and Neuropsychiatric

54
Q

Poor Prognostic Factors for Sarcoidosis ?

A

Factors associated with poor prognosis

insidious onset, symptoms > 6 months

absence of erythema nodosum

extrapulmonary manifestations: e.g. lupus pernio, splenomegaly

CXR: stage III-IV features

black African or African-Caribbean ethnicity

PS - MOST Sarcoidosis resolves without treatment

55
Q

Surgical Contraindication for NSCLC ?

A

Mediastinoscopy before CT TRO Mediastinal LN

Surgical Contraindications

  1. SVCO
  2. Vocal Cord Paralysis
  3. Tumor near Hilum
  4. Malignant Pleural Effusion
  5. FEV1<1.5 (<1.5 for Lobectomy and <2 for Pneumonectomy)
56
Q

Cavitating Lesions Mnemonic

A

WAP RATS
(Wet Ass Pussy RATS)

Wegners, Abscess, PE
RA, Aspergillosis, TB, SCC

57
Q

Alpha 1 Antitrypsin Deficiency
1. MOA
2. Inheritance
3. Treatment

A

Serine protease inhibitor (serpin) –> Inhibit Neutrophil Elastase —> Prevent Alveolar Breakdown

Autosomal Recessive / Co-Dominant
Chromosome 14

Alpha 1 Antitrypsin Concentrates
Lung Volume Reduction Surgery

58
Q

A1AT Deficiency Genotypes

A

alleles classified by their electrophoretic mobility - M for normal, S for slow, and Z for very slow

normal: PiMM

heterozygous: PiMZ
evidence base is conflicting re: risk of emphsema
however, if non-smoker low risk of developing emphsema but may pass on A1AT gene to children

homozygous PiSS: 50% normal A1AT levels

homozygous PiZZ: 10% normal A1AT levels

59
Q

How does Sarcoidosis Cause Hypercalcemia

A

Macrophages activate 1 Alpha Hydroxylase –> Activated Vitamin D3 –> Increase Calcium Absorption via Intestine DCT

60
Q

Cherry Red Lesion on Bronchoscopy THINK WHAT ?

A

Lung Carcinoid

61
Q

Why give Corticosteroids in COPD ?

A

Reduce Frequency of Exacerbations

62
Q

Isocyanates associated with which Cancer

Polyvinyl Chloride ?

Aromatic Amines ?

A

Squamous Cell Carcinoma

Angiosarcoma of Liver

Bladder Ca

63
Q

Occupational Asthma Diagnostic Investigation

A

Serial Peak Flow at Home and Work

64
Q

Most Common Chemical Associated with Occupational Asthma

A

Isocyanates

65
Q

Squamous Cell Cancer

A

Most Common Cancer in UK
Cavitates
PTHrP
HPOA and Clubbing
Central

66
Q

Sarcoidosis CXR Classification ?

A

Sarcoidosis CXR
1 = BHL
2 = BHL + infiltrates
3 = infiltrates
4 = fibrosis

67
Q

Bronchiectasis and Bilateral Hilar Lymphadenopathy NOT caused by ????

A

Amyloidosis

68
Q

B/L Hilar Lymphadenopathy Causes ?

A

Berylliosis
Histoplasmosis
Coccidioidomycosis

69
Q

Subfertility + Recurrent Chest Infections + Quiet Heart Sounds ?

A

Kartagener Syndrome

Do Sweat Test TRO Cystic Fibrosis (Absence of Vas Deferens - Normal Sperms but just less

70
Q

PAH Diagnostic Criteria

A

Pulmonary Arterial Pressure >20

71
Q

Primary Spontaneous Pneumothorax Management

A

OP Follow up every 2-4 days ambulatory

72
Q

Secondary Spontaneous Pneumothorax Management

A

Inpatient

OP Follow-up once stable in 2-4 weeks

73
Q

Hertford Syndrome Triad

Lofgren Syndrome Triad

A

CHRONIC Fever + Triad of 1. Parotitis
2. Anterior Uveitis
3. Facial Palsy

ACUTE Fever + Triad of
1. Erythema Nodosum
2. Migratory Polyarthritis
3. B/L Hilar Lymphadenopathy

74
Q

Jüngling’s disease what is it ?

A

Chronic Sarcoidosis with Cystic Bony Lesions in Acral Region (Fingers)

75
Q

Mnemonic for Occupational Asthma Chemicals ?

A

GF works at PEPSI factory and comes home daily with Asthma symptoms

GF— Glutaraldehyede. Flour

PEPSi :
Platinum salt
Epoxy resins
Proteolytic enzymes
Soldering flux resins
Isocyanates

76
Q

Mat Worker Lung Organism

Mushroom Worker Lung

Farmers Lung

A

Aspergillus clavatus

Thermophilic actinomycetes

Saccharopolyspora rectivirgula

77
Q

Is Coal Dust Associated with Lung Cancer ?

78
Q

Do we need follow-up for Pleural Plaques on CXR ?

A

NO they aren’t premalignant

79
Q

Cystic Fibrosis Features

A

short stature
DM
delayed puberty
rectal prolapse (due to bulky stools)
nasal polyps
male infertility, female subfertility

80
Q

ARDS Diagnostic Criteria

A

2012 Berlin definition: remember as ABCD

A: Acute onset (within 1 week of lung injury)

B: bilaterafl infiltrates on CXR

C: (not) cardiogenic

D: Decreased PaO2:FiO2 (mild <300, mod <200, severe <100)

HYPOXIC despite Oxygenation

81
Q

Mechanism of Action of LTRA

A

Binds to CysLT1 Receptors

Blocking action of cysteinyl leukotrienes in Bronchial Tissue which are released by Immune System to increase mucus secretion, bronchoconstriction etc …

82
Q

Investigation of Choice for Fixed Upper Airway (Tumor, Goiter etc… )

A

Flow - Volume Loops

83
Q

Asthma workup (New Guidelines) for >16

A
  1. Eosinophilia or FeNO (>40ppb)
  2. BDR (FEV1>12% or 200mls Pre and Post BD OR >10% of Predicted)
    If Unavailable then PEFR
    3.Twice Daily for 2 weeks (20% variability)
  3. Bronchial Challenge Test

If NO for BDR Test then Straight to Bronchial Challenge Test

84
Q

Asthma Workup for 5-16 y/o

A

SAME as above but

FeNO > 35ppb
NO Eosinophilia

1, 2, 3 same but 4 is

  1. Skin Prick for House Mite OR Total IgE raised

If Yes –> Eosinophils >0.5*10^9 ? –> If NO then Refer for 2nd Opinion and Bronchial Challenge Test

85
Q

Asthma Workup for <5y/o

A

Any Preschooler with 1 hospital admission OR >/= 2 ED admissions WITHIN 12 months