Respiratory Flashcards

(106 cards)

1
Q

What are some indication for VATS procedure?

A

wedge resection/segmentectomy
lobectomy
decortication
bullectomy
tx of recurrent pneumothorax

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2
Q

What are the benefits of video-assisted thoracoscopic surgery over open
thoracotomy?

A

Smaller incision so less:
pain
wound complications
healing time
length of stay

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3
Q

What are the possible indications for a lobectomy?

A

Lung ca
Aspergilloma
Tuberculosis
Lung abcess

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4
Q

How would you Ix ?lung ca, after CXR?

A

staging CT TAP
Tissue diagnosis - bronch/EBUS/CT guided biopsy
If curative - PET

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5
Q

How would you work up a patient for lung surgery?

A

hx and exam
PFTs inc transfer factor
cardiopulmonary exercise testing

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6
Q

When performing a lobectomy, what FEV1 would you want the patient to have?

A

FEV1 at least 1.5

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7
Q

When performing a pneumonectomy, what FEV1 would you want the patient to have?

A

FEV1 2

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8
Q

Do you know of a VO2 max threshold which offers a better post- operative
prognosis for the patient?

A

at least 15mg/kg/min

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9
Q

Tell me about the different histological cell types of lung cancer

A
  • SCLC 20%
  • NSCLC (adenocarcinoma, SCC, broncheolar carcinoma, large cell carcinoma, neuro endocrine)

most common: SCC, then adenocarcinoma

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10
Q

What’s the treatment for SCLC?

A

rarely operable
limited disease - chemo/radio
late disease - palliative chemo

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11
Q

What’s the treatment for Non SCLC?

A

curative surgery/radical radiotherapy for early disease
chemo/molecular therapies if more advanced

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12
Q

If VATS had been done recently what would you expect?

A

Tracheal deviation towards side
Reduced air entry

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13
Q

Reasons for bilateral lung surgery

A

Bilateral apical pleurectomies for recurrent pneumothoraces
Lung volume reduction eg bullectomy
TB

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14
Q

What inhalers can you use for COPD?

A

short acting beta - salbutamol
short acting mucs - ipratropium
long acting beta - salmeterol
long acting musc - tioptropium

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15
Q

Clinical findings for pneumonectomy vs lobectomy?

A

Pneumo
- trache deviated
- absent breath sounds
- dull percussion
Lobe
- trache might/not be deviated
- breath sounds normal/reduced
- percussion normal

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16
Q

What are the respiratory causes of clubbing?

A

ILD
CF
Lung abscess
Bronchiectasis
Lung ca

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17
Q

Whats the difference between primary and secondary pneumothorax?

A

Primary - spontaenous in otherwise healthy person
Seconday - some form of ILD

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18
Q

What the initial management of breathless primary spontaneous pneumothorax?

A

ABCDE, rapid escalation, senior help
Try to aspirate up to 2.5l litres
If stops being breathless or residual <2.5cm - home w OP FU
If not drain
<2cm and asx - conservative with early FU

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19
Q

Is there any role for suction in the management of a pneumothorax?

A

Rarely used due to risk of re-expansion pulmonary edema
High volume, low pressure recommended

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20
Q

Management of patients with on-going air leak or recurrent pneumothoraces

A

Talc pleuradhesis/pleurectomy
Bullectomy
Surgery/VATS
VATS has 5% chance of recurring pneumothorax vs 1% for open surgery

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21
Q

Differentials for normal chest exam apart from scars

A
  • *Wedge resection** - pulmonary nodule
  • *Lung biopsy**
  • *Pneumothorax** -Surgical tx/non resolving/recurrent
  • *Lobectomy** - long time ago
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22
Q

How would you investigate a patient with asthma?

A

Baseline obs inc sats
Bloods inc CRP
ABG
Skin prick/RAST
CXR
PF
Spirometry

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23
Q

What would you look for in FBC for asthma?

A

WCC - infection/steroids
Eosinophilia

IgE also important

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24
Q

Relevance of PF in asthma

A

Diurnal variation shows not well controlled
Reduction early morning

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25
How might a spirometry in an asthma patient differ than in a patient with chronic obstructive pulmonary disease?
COPD - obstructive spirometry, reduced FEV1 preserved FEC, reduced FEV1FVC ratio asthma is reversible obstruction (whereas COPD is fixed), should show improvement following bronchodilator by 200ml PF or 15%
26
How do you treat asthma?
BTS guidelines 1st - SABA 2nd - inhaled steroid 3rd - LABA 4th - LRA
27
What are some causes of air flow obstruction?
Bronchiectasis COPD Obliterative bronciolitis
28
What does polyphonic wheeze indicate?
Airflow obstruction
29
Causes of wheeze?
Asthma COPD Pulmonary edema
30
What is obliterative bronchiolitis?
Fixed airflow obstruction Secondary to viral infection, polutants or following stem cell transplantations or GvsH
31
What's the definition of reversible airflow obstruction?
significant change in either FEV1 or peak expiratory flow rate, in response to a short acting beta-agonist 200ml or 15% change uncontrolled asthmatics tend to have \>400ml change
32
Differentials of bibasal inspiratory creps?
Bronchiectasis (coarse, clear on coughing) B/L pneumonias CCF (elevated JVP, peripheral edema)
33
Investigations for ILD?
Obs inc sats FBC - anaemia, infection U+Es, LFTS - MEDS **Autoimmune** - RF, dsDNA, ANA, ACNA **RAST/allergens/av avian precipitans** ABG CXR **HRCT** - honeycombing (fibrosis), groundglass - alveolitis **Echo** - Right sided heart strain/failure, PHTN **Spirometry** **BAL/lung biopsy**
34
What are the typical lung function characteristics associated with pulmonary fibrosis?
spirometry tests - restrictive pattern reduction in the FEV1 and FEC,a preserved ratio reduced total lung capacity reduced transfer factor.
35
How do you treat ILD?
MDT Physio, OT, resp nurses if tx connective tissue disorder DMARD groundglass might be **steroid** response idiopathic pulmonary fibrosis - anti fibrotic agent e.g **pirfenidone**
36
Cuases of lower zone fibrosis SAB IPM
Systemic sclerosis/RA/SLE Alpha 1 anti tryspin, ABPA Bronchiectasis Infection Medications - bleomycin, nitro, hydralazine, methrotrexate, amiodarone Clubbing + \>50 suggests IPF
37
Causes of apical fibrosis | (CASH RAT)
Silicosis Coal workers pneumoconiosis Histiocytosis Ank spond ABPA Radiation TB
38
What's next line if Ix suggest pulmonary fiborsis?
FVC \<80% refer to tertiary care for pirfenidone/nintedanib Then MDT ax, surgeons ?lung transplant
39
Substance exposure that can cause ILD
Asbestos Radiotherapy Siclia/berylium Birds Amiodarone/methotrexate
40
Examples of idiopathic interstitial pneumoniae
desquamative interstitial pneumonia respiratory bronchiolitis interstitial lung disease **(RB-ILD)** acute interstitial pneumonia **(AIP)** nonspecific interstitial pneumonia **(NSIP).**
41
Examination findings suggesting CF
Coarse crackles loudest in upper zone - broncheictasis Portacath scar chest/axilla Clubbing PEG O2 Signs of CF
42
Whats the cause of cystic fibrosis?
Auto recessive mutaton in CFTR Increased salt excretion causing thicker mucus affects rep, disgestive tract, reproductive system
43
Features of CF
_Multi system disease_ bronchiectasis pancreatic insufficiency - Creon + fat soluble vitamins Liver - cholestasis, gallstones, cirrhosis, liver failure Kidney stones Reproductive issues
44
How you would manage someone with cystic fibrosis?
**MDT,** speciailist centre **Physio** - postural drainage, enhanced breathing techniques to clear mucus from chest **Dieticians -** supplements, gastrostomy Regular **nebs** - muclotyics, nebulised ABx prophylaxis, recombinant DNAse, hypertonic saline **ABx** PO azithromycin, regular IV ABx 2/52 course **Pancreas** - Creon, vitamins, high calorie diets **Gene** therapies under development
45
Explain the microbiology of cystic fibrosis lung disease.
most common **Pseudomonas aeruginosa** **Burkholderia cenocepacia** and **mycobacterium abscessus****poor prognosis**absolute**contraindication**to lung**transplantation**.
46
Explain the genetics of CFTR
autosomal recessive genetic mutation chromosome 7 in production of defective CFTR Lots of different mutations, most common in UK is DeltaF508 now known as Ph508del 508 deletion 50% of UK are homozygous
47
Describe the nutritional issues in CF
Pancreatic insufficiency catabolic state due to chornic infection leading to high calorie requirements often low BMI + signs of supplemental feeding CF patient can have button PEG tube which lies flush with skin so less detectable Also CF related diabetes
48
Non resp features of CF
CF liver disease - PHTN, Hypersplenism Osteopaenia/porosis, low impact fractures eg coughing Infertility - absent vas deferns men Sinus disease/nasal polyps Constipation/meconium, distal intestinal obstruction Gallstones, kidney stones
49
Respiratory complications of CF
ABPA Pneumothoraces Bronchiectasis Haemopytsis - may require bronchial artery embolisation
50
How is CF diagnosed?
All newborns tested as part of Guithrie Immunoreactive trypsin levels via heelprick - if raised CF suspected then screened for most common CTFR mutations + sweat test - abnormally high chrloide content \>60mmol
51
52
What does a clam shell scar indicate?
Double lung transplant Likely accompanied with: inter costal drain scars trache scars centrail line scars hand tremor - transplant meds clubbing ?fibrosis ?bronchiectasis
53
How can you tell from examination if lung transplant is working well?
If not working: Supplemental O2 Cyanosis
54
What are the most common indications for lung transplant?
CF Bronchiectasis pulmonary vascular disease pulmonary fibrosis COPD (single lung)
55
What would be the usual indications to a double lung transplant, and why would you do a double over a single transplantation?
Double transplant prognosis is better CF and bronchiectasis usually have double, plus some pulmonary vascular and PF
56
medications used in lung transplantation
Usually combo: tacrolimus + mycophenolate/azothioprine + steroid cyclosporin was used but now less as causes renal impairment
57
Can you tell me about complications of lung transplantation?
Acute - hyper acute rejection, opportunistic infection (Causing damage to transplant) Becomes progressively more susecptible to broncilitis obliterans over time, eventually causes resp failure and death
58
Do you know of any contraindications to lung transplantation?
* **malignancies** within the last five years * v high or low **BMIs** * **smoking** or using illicit drugs * **mental health** conditions won't take medications on a regular basis/ regularly turn up to clinic appointments. severe atherosclerotic disease, infection, poor functional status, no social support
59
Scars that indicate lung transplant
Clamshell - double Median sternotomy and/or lateral thoracotomy - single lung/heart Drains Central line trache
60
Criteria for lung transplant
1. **\> 50% risk death** from lung disease within **two years** if transplant is not performed 2. **\> 80% likelihood** of **surviving** at least 90 days post-transplant 3. \> 80% likelihood of a 5-year post-transplant survival from a general medical perspective provided there is adequate graft function. Median surival is around 6 years, worse in COPD and PF i.e sick enough to need transplant but well enough for it to work
61
What's the main cause of chronic lung transplant rejection?
Bronchilitis obliterans + infection, malignancy (lymphoproliferative, skin
62
Complications of immuno suppresion
**Malignancy** - lymphoproliferative, skin Steroids - DM, osteoporosis, skin thinning, **cushings** Tarcolimus - tremor ABx and anti rejection meds - hearing and **renal impairment**
63
When to refer for lung transplant
All UIP or fibrotic NSIP otherwise **FVC \<80%** **transfer factor \<40%** CF
64
Which COPD patients benefit most from lung transplant
BODOE \>6 (COPD survival score) | (SOB, FEV, ET, BMI)
65
Yellow nail syndrome - discolored, hypertrophie, thickened
66
Possible examination findings of yellow nail syndrome
Creps clear with coughing - **bornchiectasis** Dystrophied, thickened discolored **nails** Wheeze, productive cough Long term venous access Cor pulmonale **Pleural effusion** **Lymphedema**
67
Ix for bronchiectasis
Routine bloods HIV/immunoglobulins Aspergillous serology CF if \<40 sputum culture PFTs CXR HRCT
68
Management of bronchiectasis
Physio - postural drainage Nebs - hypertonic saline, sometimes neds eg psuedomonas Long term ABx - azithromycin 2 weeks of ABx guided by sputum MCS PEEP Flu +pneumococcal vax carbocisteiene Surgcial if severe despite max med rx
69
Causes of bronchiectasis
Immunodeficiency Connective tissue eg RA IBD Lobar pneumonia pulmonary TB fungal mould eg ABPA
70
If you had a patient in whom you suspected bronchiectasis, what sort of questions would you ask in their clinical history?
Chest pain Cough - ?productive ?volume of sputum ?number of infections/year, SOB/wheeze, haemopytsis GI sx (IBD) joint pain/swellings travel ?TB prev severe chect infection eg pertusiss, TB CF - steotorrhae, BMI, fertility (also cilliary dyskinesia, nasal biopsy)
71
Examination findings to look for ax conditions in bronchiectasis
IBD (abdo scars) RA joints Clubbing eg CF
72
If you had a suspected a patient had lung cancer how would you proceed with investigations?
Bloods: * FBC - anaemia * CRP - infection/malignancy * LFTs - liver mets, future tx * U+Es - hyponatraemia SLCL, future tx * clotting ?intervention Spirometry ?lung function/futness for surgery Sputum CXR staging CT CT TAP
73
If you only have a CT scan and that looks like the patient has lung cancer. How would you then proceed?
The next step would be trying to identify a tissue diagnosiS via: o bronchoscopy o ultrasound-guided bronchoscopy o percutaneously via a radiologist. + lymph nodes, pleural effusion if curative PET CT
74
How might someone present if they have lung cancer?
* persistent cough +- haemoptysis * weight loss * voice change * SVCO - face.arm swelling, distended veins * thirst/bone pain/confusion * collapse/effusion +-trachea deviated, reduced percussion * monophonic wheeze from tumour * Horners if apical
75
Hypertrophic Pulmonary Osteoarthropathy HPOA
76
Cause of hypercalaemia in lung Ca
bone mets ectopic PTH secretion
77
Management of lung ca patients with stage 4 disease
Usually palliative If NSCLC molecular therapies
78
Hormonal issues ax with SCLC
Lambert Eaton SIADH ectopic ACTH
79
wasting small muscles of hands
80
Causes of exduative pleural effusion (ie no other signs of overload)
* parapneumonic effusions * lung **infarction** eg from *PE* * lung **malignancy** * **connective tissue** disorders eg RA PE, lymphoma, vasculitis
81
Causes of transudative effusions (ie with overload)
CCF Liver failure CKD Hypoalbuminaemia PE, myoxedma, periotneal dialysis
82
How do you tell between a transudative and exudative effusion?
Lights criteria 1. Pleural/serum protein is \>0.5 2. Pleral/serum LDH \>0.6 3. Pleural LDH greater than 2/3 upper limit of normal serum LDH
83
What would you want to test for in pleural fluid sample?
* pH * MCS * cell count * cytology * glucose * triglyceride AFB ?TB (e.g RA or chylous effusion
84
Indications for drainage of pleural effusion?
If pH \>7.2/frank pus/culture positive/large and sx drain
85
If this patient had a pleural effusion secondary to a primary lung cancer. How would you manage that?
drain and then long term catheter or pleuradhesis at bedisde or via thoracoscopy
86
What does low pleural glucose indicate?
Infection Malignancy Esophageal rupture **\<1.6 RA**
87
Causes of high glucose in pleural fluid
Pancreatits
88
What kind of lung cancer would require a lobectomy?
NSCLC if caught early (SCLC is often disseminated and therefore not good for surgery)
89
Eligibility criteria for surgery for NSCLC?
patient preference, co morbidities etc lobectomy needs FEV1 of \> 1.5 litres ▪ pneumonectomy FEV1 of \> 2 litres. • Cardiopulmonary exercise testing \>15 mls/kl/minute confers a better prognosis.
90
Most common cancer in smokers
Squamous cell
91
Postero lateral thoractomy scar - pneumonectomy
92
Reason for pneumonectomy \>lobectomy in NSCLC
involves both the upper and lower lobe/ tumour particularly central excision of just one lobe not possible
93
Anterior mediastinotmy - Chamberlain prodecture scare to access aortic arch, lymph nodes, mediastinal mass etc
94
VATS ports + anterolateral
95
What questions would you ask to try and find out underlying cause of ILD?
Asbestos Meds - amiodarone, methotrexate, nitro, chemo eg bleomycin connective tissue/RA back probs 0 ank spond
96
What drug treatments are used for interstitial lung disease?
• IPF: **pirfenidone o nintedanib.** For patients with non-specific interstitial pneumonia: o Steroids o Immunosuppressive therapy.
97
Signs of PHTN or cor pulmonale on examination
RVH raised JVP SOB edema loud s2
98
What tests would you do to Ix SOB with normal examination?
FBC/U+eS/LFTS/TFTS/ CXR/ECG Auto immune/vasculitic screen CTPA hrct PFTS inc transfer factor ABG Sleep studies
99
Differentials of SOB with normal examination
Anaemia Ca Obesity hypoventiliation syndrome Hyperventiliation
100
What would you expect the arterial blood gas findings to be in someone with obesity hypoventilation?
T2RF
101
What are the usual spirometric findings in someone with Chronic Obstructive Pulmonary Disease?
Obstuctive FEV2/FVC ratio \<0.7
102
How would you classify the severity of Chronic Obstructive Pulmonary Disease via Spirometry?
FEV1 vs predicted 1. \>80% predicted mild 2. 50-80% moderate 3. 30-50% severe 4. \<30% very severe
103
What is cor pulmonale?
Right sided heart failure secondary to resp disdease in chronically hypoxic patients chronic hypoxia causes pulmonary vasocontriction causing PHTN then Right sided heart failure
104
Rx of cor pulmonale
LTOT (reduces the pulmonary vasoconstriction) Diuretics
105
What is LTOT?
• Long term oxygen therapy is classically oxygen which is given for at least 16 hours a day in order to treat patients who are chronically hypoxic, to reduce the risk of Cor Pulmonale.
106
LTOT Indications
* Non‐smoker * PaO2 \<7.3kPa on air * PaCO2 that does not rise excessively on O2 7.3-8 if: • secondary polycythaemia • pulmonary hypertension • peripheral oedema