Respiratory for long case Flashcards

1
Q

Lung disease severity measures - history

A
  • Exercise tolerance, up flights stairs
  • Ability to be comfortable, speaking in sentences
  • Frequency of exacerbations
  • Frequency of hospital admissions
  • Frequency of respiratory infections
  • Frequency of intubations
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2
Q

Lung disease severity measures - exam

A
  • Respiratory rate
  • Acute irritability
  • Low sats and oxygen requirements
  • cyanosis
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3
Q

Lung disease severity measures - investigations

A
  • FEV1 and FVC
  • DLCO
  • Oxygen saturation and concentration on arterial blood gas
  • Degree of hypercapnoea and compensation for respiratory acidosis
  • Pulmonary pressure on TTE
  • VO2 max on exercise testing
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4
Q

Adherence measures/history - cardiorespiratory

A
  • Regular use of inhalers with correct use of spacer and medications
  • Smoking cessation
  • Peak expiratory flow measures on regular basis
  • Use of action plan
  • Regular GP and specialist appointments
  • Yearly influenza vaccinations, completed pneumococcal vaccinations
  • Avoidance of potential triggers
  • Involvement in rehabilitation and exercise program
  • Involvement of loved ones, community support in care
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5
Q

Bronchiectasis risk factors

A

recurrent childhood infections

immunodeficiency

abnormal mucociliary drainage – CF, kartager’s syndrome

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6
Q

complications of bronchiectasis

A

o Frequency of pneumonia, courses of antibiotics

o Abscess, empyema and thoracic decortication surgery (time of surgery, management, complications)

o Recurrent pleurisy – severity of symptoms, impact on life, management

o Colonisation with resistant organisms – recent cultures, eradication with Abx

o Pulmonary hypertension and right heart failure

o Bronchial haemorrhage requiring bronchoscopy and cautery

o Amyloidosis

o Other systemic infections (infective endocarditis)

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7
Q

Diagnosis of CF

A

CT

sweat testing

ciliary function testing

bronchoscopy

immunoglobulins

eosinophilia (allergic bronchopulmonary aspergillosis)

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8
Q

Treatment of bronchiectasis

A

o Sputum clearance

o Antibiotics

o Bronchodilators

o Inhaled steroids

o Oral steroids

o Twice daily postural drainage

o Vaccination

o Treatment of HF

o IV immunoglobulin

o Bronchoscopy of haemoptysis

o Lobectomies, wedge resections for localised drainage

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9
Q

Lung carcinoma - local symptoms

A

o Reduced exercise tolerance

o Pleural and thoracic chest pain (pleural and thoracic wall involvement)

o Dysphagia, hoarseness, stridor (tracheal and oesophageal obstruction)

o Headache and dizziness (superior vena caval obstruction)

o Bony pain, abdominal pain (metastasis)

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10
Q

lung carcinoma - systemic symptoms

A

o Loss of weight, appetite, night sweats

o New paraesthesia, weakness unsteadiness (LEMS, peripheral neuropathy, cerebellar degeneration, polymyositis and dermatomyositis, acute transverse myelitis)

o Limb pain, purpura (DVT, DIC)

o Polyuria (hypercalcaemia)

o Acanthosis nigricans, scleroderma

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11
Q

Lung carcinoma - investigations

A

o CT scans, biopsy -bronchoscopy or CT guided, VATS pleural, pleural tap

o Staging -CTCAP, PET scan

o PFTs for fitness for surgery FEV1 >1.5L

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12
Q

Lung carcinoma - treatment

A

o Chemotherapy – weekly/fortnightly course number of courses

 Antiemetic therapy, chemotherapy nursing support

 In hospital, clinic, home

o Radiotherapy

 Brain – prophylactic

 Chest –

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13
Q

Complications of lung carcinoma - disease

A

o Progression of local disease, metastasis – liver, abdominal, bony involvement

 Cord compression ascites biliary sepsis obstructive pneumonia DVT/PE

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14
Q

Complications of prednisolone treatment

A

 Myopathy

 Opportunistic infections

 Mania/psychosis

 Osteoporotic fractures

 Dysmorphic cushingoid features

 BSL derangements, refractory hypertension

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15
Q

Chemotherapy SEs lung cancer

A

 Nausea vomiting

 Mucositis

 Typhlitis, neutropaenic sepsis

 Peripheral neuropathy and pain

 Ototoxicity

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16
Q

Complications lung Ca - cancer pain

A

 Degree of opioid requirement

  • Number of rotations
  • Overdoses

 Local nerve blocks

 Functional loss due to pain

 Degree of sleep loss

 Degree of emotional distress

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17
Q

Measures of response - lung cancer

A

 Surveillance scans and PET post treatment course

 Blood counts, BMT myeloid/lymphoid malignant cell counts

 Blood tests – CA199, PSA

 Degree of functionality – walking, daily activities, ability to walk, moods  Level of pain

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18
Q

COPD precipitants

A

o Upper and lower respiratory tract infections

o Omission of medications

o Heart failure

o Sleep apnoea

o Pneumothorax

o GORD

o aspiration

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19
Q

COPD diagnosis

A

o Initial symptoms, spirometry – bronchodilator responsiveness, CT, arterial blood gases, FVC, FEV1

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20
Q

Complications of COPD

A

o Number of hospital admissions

o Number of exacerbations

o Number intubations

o Current exercise tolerance, flights of stairs, things unable to do

o FEV1, 6 minute walk test

o Oxygen concentration on arterial blood gas

o Current weight and degree of weight loss

o Pulmonary hypertension and right heart failure

o Lung cancer (separate issue)

o Depression (separate issue)

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21
Q

ECOG

A

0 Acute without restriction of performance

1 Ambulatory and able to attend light work activity, unable to carry out strenuous activity

2 Can manage self-care but unable to attend any form of work activity, ambulatory for more than 50% of the time while awake

3 Can manage one limited self care, bed bound for more than 50% of the time

4 Disabled, completely bed bound

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22
Q

Smoking - history

A

 Amount smoked

 Evidence of nicotine dependence –

smokes >10/day

30mins between smokes

smoking from waking

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23
Q

Smoking - high risk groups

A
  • Pregnancy
  • Parents of young children
  • Aboriginal and torres strait islanders
  • Mental illness
  • Other substance abuse
  • Lung disease
  • CVD risk factors and diabetes
  • Low socio-economic status
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24
Q

Smoking - Initial management

A

brief advice, motivational interviewing, quit date Follow up - Relapses occur in first few weeks of quitting and require follow up • Associated with weight gain, stress, and withdrawal symptoms

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25
Q

Smoking - pharmacological therapy

A

 NRT increases quit rates by 60% from placebo, combination therapy oral and patch more effective than one alone CI – pregnancy, arrhthymias, lactation, CVD, angina, stroke

 Varenicline – most effective, doubling abstinence rates, nausea; CI neuropsychiatric disease; however no increase in SI

 Bupropion – effective with social support

  • CI in seizures, CNS disease, PD MAOI treatment;

caution in DM, CKD, other drugs that may reduce seizure threshold

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26
Q

Current COPD treatment

A

o Bronchodilators and spacer

o Domociliary oxygen – ABG, desaturation on 6MWT

o Annual influenza vaccinations o BiPAP

o Number of prednisolone courses

o Pulmonary rehabilitation attendance, number of times, usefulness o Lung valves, lobectomies

o Transplantation work up (separate issue)

o Antiprotease therapy for alpha1 antitrypsin

o Frusemide for RHF

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27
Q

COPD - asthma ddx

A

Non smoker

Childhood onset

Allergy

Nocturnal symptoms

Rapid response to treatment

Eosinophila in sputum

Bronchodilator reversibility

Atopy

28
Q

COPD - bronchiectasis ddx

A

Daily sputum expectoration

Childhood recurrent chest infections, pertussis

Clubbing

29
Q

COPD examination

A
  • Pursed lip breathing
  • Cyanosis/polycythaemia
  • Intercostal recession
  • Prolonged forced expiration
  • Tracheal tug
  • Reduced diaphragmatic movements
  • Reduced chest wall expansion
  • Hoover’s sign
  • Reduced breath sounds w/ wheeze
  • Sputum
  • RHF – parasternal heave, cv JVP, palpable P2, pulsatile liver
  • Cachexia
30
Q

Sleep apnoea - history

A
  • History – symptoms/concern leading to sleep study
  • Use of hypnotics
  • Evidence of paroxysmal nocturnal dyspnoa, orthopnoea, sensation of choking
  • Driving – heavy machinery licence, adherence to driving restrictions
31
Q

Risk factors OSA

A

obesity

daytime sleepiness

alcohol

hypertension

atrial fibrillation

GORD,

COPD

systolic heart failure

deviated nasal septum

nasopharyngeal deformity or tonsillar enlargement (if no obvious obesity)

32
Q

Epworth sleepiness scale

A

o Reading

o TV

o Theatre or meeting

o Driving as a passenger > 1hr

o Lying in afternoon

o Sitting and talking

o Sitting after lunch

o Dozing at traffic lights

33
Q

Components of sleep study

A

o Electroencephalogram o Apnoea/hypoapnoea index o Chin myogram o Electro-occular monitoring REM sleep o Sats probe o ECG overnight

34
Q

Managment OSA

A

o Use of CPAP

 Adherence, nose bridge ulcers, uncomfortable mask, dyspnoea/anxiety in mask

 Improvement in sleepiness

o Weightloss

o Surgical correction of upper airway

35
Q

OSA exam

A
  • Malampatti score
  • Neck circumference
  • BMI - Hip/waist ratio
  • Acanthosis nigricans
  • Evidence of nasal bridge ulcers
36
Q

Interstitial lung disease - symptom history

A

o Dry cough, worsening dysponea

o History of pneumothorax, young woman

o Systemic/rheumatic symptoms

o History of asthma -> Churg-Strauss syndrome

o Haemoptysis/renal disease – Goodpastures/SLE

37
Q

Interstitial lung disease - drug/RTx history

A

 Cardiac/anti-arrhythmic – amiodarone, procainamide

 Hydralazine

 Rheumatologic – MTX, penicillamine

 Chemotherapeutics – bleomycin, bisulphin

o Prior radiotherapy

38
Q

Interstitial lung disease - rheumatic symptoms

A

Raynauds

Polyarthritis

Rashes

Morning stiffness

Generalised malaise, LOW, LOA, sweats

Pleural lung disease, pericarditis

39
Q

Interstitial lung disease - occupational history

A

 Silica, asbestos, coal

 Nitrogen, chloride gas, ammonia gas

 Brake fluid, vinyl chloride

40
Q

Interstitial lung disease - Hypersensitivity exposure

A

 Bird, farmers – mouldy hay/grain

 Cotton (byssinosis), flax/hemp dust

o History of tuberculosis exposure

41
Q

Interstitial lung disease - investigations

A

o CT chest – fibrosis, usual interstitial pneumonia (honey combing, subpleural basal predominance, traction bronchiectasis), Non-specific interstitial fibrosis

o Brochoscopy and lavage w/ biopsy

o ESR, CRP, ANA/ENA ABG

42
Q

Interstitial lung disease - treatment

A

o Remove exposure, steroids – hypersensitivity, COP, sarcoidosis, CTD, histiocytosis X

o Nifedipine

o Lung Tx

o Home O2

43
Q

Investigations for pulmonary HTN

A

TTE, cardiac catheterisation, PFT, CT chest, V/Q, CTPA, HRCT, 6 minute walk test

44
Q

Risk factors for Pul HTN

A

o Prior PE, COPD, heart failure, family history, gene testing (BMPR2), HIV, interstitial lung disease, sleep apnoea, scleroderma/MCTD

45
Q

Medications for pul HTN

A

warfarin, bosentin, sildenafil, prostacyclin (SE: flushing)

46
Q

History for sarcoidosis

A

o Systemic symptoms

o Joint symptoms and rash

o Eye involvement – uveitis

o Sinusitis, parotiditis

o Renal stones

o Nerve palsies

47
Q

Differentials for sarcoidosis

A

o Connective tissue disease

-SLE – joint/rashes, mucosal involvements, RA, seronegative arthritis, sjogrens o Bechet’s disease

– genital and mucosal ulcers, family history o Vasculitis

– Granulomatous polyangiitis, eosinophilic polyangiitis, polyarteritis nodosa, GCA/PMR +/- glomerulonephritis

o Antiphospholipid syndrome

o Lymphoma, paraproteinaemia, POEMS, castleman’s

o Subacute infective endocarditis

o Atrial myxoma

o Cholesterol emboli – recent angiography

o Tick disease

o Hypothyroidism/hyperthyroidism

48
Q

Symptoms of hypercalcaemia in sarcoid

A

o Polyuria, polydipsia, confusion

49
Q

Investigations for sarcoidosis

A

o ESR, CRP, ANA/ENA/ANCA, dsDNA, SPEP, immunoglobulins, TFTs, FBE, CMP, Vitamin D, CT chest, TTE, blood cultures bone marrow biopsy

50
Q

Cystic fibrosis - systemic involvement

A

o Recurrent pneumonia, pleurisy, effusion, empyema and abscess

o Bronchiectasis

o Nasal polyps

o Pancreatic failure - malabsorption,

o small bowel obstruction

o Focal biliary cirrhosis

o Exocrine diabetes mellitus

51
Q

Cystic fibrosis - investigations

A

o Sweat/chloride testing

o PCR/DNA gene marker

o Spirometry FEV1, CT scans

o Sputum cultures, colonisation

o FBE for anaemia of chronic disease, IDA, and B12 deficiency o LFTs, INR, abdominal USS, AFP, gastroscopy for varices

52
Q

Cystic fibrosis - complications

A

o Haemoptysis

o Pneumonia

o Empyema

o Pleurisy

o Pneumothorax

53
Q

Management of cystic fibrosis

A

o Physiotherapy

o Exercise tolerance o Pancreatic enzyme supplementation

o High fat diet

o Recombinant DNAase - Transplantation work up o Regular appointments

o Fertility, consideration of IVF

54
Q

Indications for lung transplant

A

COPD FER <25%

cystic fibrosis PaCO2 > 55, FER < 30%

ILD DLCO <20%, symptoms

eisenmengers, pulHTN – PAP >55, cardiac index <2L/min?

55
Q

Contra-indications for lung transplant

A

Relative -

T2DM ,osteoporosis, etOH, smoking, MAC/tuberculosis abscesus colonisation

wt >130% ideal <70% ideal

compliance

Absolute

HIV, HBV, HCV, malignancy <5yrs

56
Q

Transplant history

A
  • Rejection
  • HLA matching
  • Infections

– influenza, aspergillosis, CMV, myxomavirus, aspergillosis

  • Immunosuppression – renal transplant, hyperlipidaemia, post transplant lymphoproliferative disorders
  • Brochiolitis oliterans

– chronic rejection,

57
Q

COPD History

A

Smoking history, other substances

Dust, gas exposure

Chronic sputum production, cough

Exercise tolerance

Ankle swelling

Loss of weight and appetite

Frequency of exacerbation

Vaccinations

Previous lung surgery

Recent PE/DVT, pneumothoracies

Pulmonary rehab

58
Q

Investigations for COPD

A

ABG

PFT (FER <0.7, TLC high, VC low, DLCO decreased); note that dyspnoea on minimal exertion correlates to FEV1 30% of predicted

FBE Hb level, elevated if PaO2 is <55; HCT > 52% in males, 45% females signifies erythrocytosis indication for LTOT

HRCT - for emphysema and other causes of lung dysfunction

Sleep study - considered if PaO2 is high (>60) in the presence of cor pulmonale and/or polycythemia

Sputum culture indicative of moraxella catarrhalis, haemophilus influenzae and streptococcus pneumonia

Steriod challenge for FER responsiveness

59
Q

Smoking related complications

A

IHD

Peripheral vascular disease

Berger’s disease of the peripheries

Carcinoma of lung, head and neck, bladder, oesophagous, colon, renal

Osteoporosis in women

Erectile dysfunction in men

Peptic ulcers

Polycythemia

?Tobacco-alcohol amylopia

60
Q

Management of COPD

A

Instruct patient on meds

Steroids for exacerbation

Inhalers - inhaled steroids, muscarinic antagonist, beta agonist - all long acting

Phosphodiesterase 4 inhibitors

Antibiotics - if acute, prophylactic drugs

Quit smoking - nicotene patch, bupropion for anti-craving

?Oxygen supplementation - PaO2 <55mmHg or <88% sats at rest or asleep, PaO2 56-59 w/ cor pulmonale, RVH and p pulmonale on ECG, PCV > 0.55

Frusemide if cor pulmonale present

Consider transplant if <55 yrs

Nutritional advice

Vaccinations (pneumococcal, influenza)

?Alpha-antitrypsin deficiency (treat w/ smoking cessation, tamoxifen or danazol)

61
Q

Bronchiectasis History

A

Symptoms of cough and sputum production

Frequency of exacerbation (record most recent and length of stay, management each time)

Use of prophylactic antibiotics

Previous postural drainage, chest physio and mucolytics

Prior episodes of massive haemoptysis

PHx - recurrent infections, including pertussis/whooping cough, measles, TB; Alcohol use, cystic fibrosis, immunodeficiency, HIV, Asthma

Social set up - work and home stressor

Depression

62
Q

Bronchiectasis examination

A

RR, O2 sats, HR, BP

Peripheral cyanosis, clubbing

Hypertrophic pulmonary osteoarthropathy wrists and ankles

Ausculation - coarse creps and wheeze

Parasternal heave, loud P2, raised JVP, ascites, pitting oedema at peripheries, HSM

Dextrocardia (right sided heart beat - Kartagener’s syndrome)

63
Q

Management of Bronchiectasis

A

Reduce secretions - Regular chest therapy, recombinant DNAse

Prevent and treat exacerbations - Abx according to severity, regular bronchodilator +/- steroids

Treat cor pulmonale and persistent hypoxia w/ frusemide and LTOT

Treat Allergic Bronchopulmonary Aspergillosis w/ high dose steroids +/- antifungal therapy

Treat hypogammaglobulinaemia w/ IV immunoglobulins

Nutritional dietary supplements, availability of community based healthcare resources and psychological counselling

64
Q

Cystic fibrosis history

A

Age of diagnosis

Current respiratory symptoms

Epistaxis - nasal polyps, sinonasal symptoms

Recurrent admissions, abx therapy

Physiotherapy

Steatorrhoea (pancreatitis), intestinal obstruction (meconium ileus), RUQ pain (gallstones)

Pancreatic enzyme supplementation

Heat intolerance and exhaustion

FHx of CF

T2DM history

Appetite, weightloss, pancreatic supplementation

Reproductive plans

65
Q

Investigations for Bronchiectasis and CF

A

CXR - cystic air spaces, air-fluid levels in dilated bronchi, thickened bronchial walls with peribronchial cuffing- appearance of tramlines and ring shadows

HRCT

PFTs - may be obstructive/restrictive or both

Sputum microscopy and culture

FBE - anaemia of chronic disease +/- chronic haemoptysis, eosinophilia (ABPA), low alb poor prognosis, ESR, CRP

UEC for renal function

Fibreoptic bronchoscopy, sweat chloride levels >70mmol/L, serum immunoglobulin assay, sperm assay or respiratory mucosal Bx (Kartager’s syndrome/ciliary dyskinaesia), skin tests and serology for aspergillosis

66
Q

Management of Asthma

A

Optimise control - oral steroids required if SABA and IGCS not sufficient; LABA may be required if still not sufficient; leukotriene inhibitors for further control

Revise inhaler technique

Develop/revise asthma action plan - plan when symptoms worsen, PEFR measurements, self adjustment of meds, when to seek medical help

Stop smoking influenza, pneumococcal vaccinations

67
Q

Features of asthma clinical severity

A

Three or more of

Daytime symptoms > 2 per week

Need for SABA > 2 per week

Any limitation of activities

Any symptoms during night or waking