Week 3: Respiratory medicine (2) (emergencies, X-ray, infections) Flashcards

(90 cards)

1
Q

anaphylaxis

A
  • SERIOUS allergic reaction
  • Sensitised individual exposed to specific antigen
  • Commonly from insects bites/ stings, food, medications
  • Immunological response: – IgE → antigen → mast cell & basophils ‡ → histamine ↑ → body response
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2
Q

signs and symptoms of anaphylaxis

A
  • Occurs in minutes - Pruritus, urticaria & angioedema, hoarseness, progressing to stridor & bronchial obstruction, wheeze & chest tightness from bronchospasm
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3
Q

management of anaphylaxis

A
  • DO NOT DELAY! GET HELP
  • Remove trigger, maintain airway, 100% O2
  • Intramuscular adrenaline 0.5 mg (Repeat every 5 mins as needed to support CVS)
  • IV hydrocortisone 200mg
  • IV chlorpheniramine 10 mg
  • If hypotensive: lie flat and fluid resuscitate
  • Treat bronchospasm: NEB salbutamol
  • Laryngeal oedema: NEB adrenaline
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4
Q

COPD exacerbation

A
  • Infective
    • Change in sputum volume / colour o Fever
    • Raised WCC +/- CRP
  • Non-infective
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5
Q

symptoms and signs of COPD exacerbartion

A
  • More coughing, wheezing, or shortness of breath than usual.
  • Changes in the color, thickness, or amount of mucus.
  • Feeling tired for more than one day.
  • Swelling of the legs or ankles.
  • More trouble sleeping than usual.
  • Feeling the need to increase your oxygen if you are on oxygen
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6
Q

management of COPD exacerbation

A
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7
Q

classification of asthma

A
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8
Q

raised CO2 in asthma attack

A

Raised CO2 is near fatal because shows patient is getting tired and cannot blow off CO2 anymore -→ need anaesthetics and intubation

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9
Q

management of acute asthma

A
  • ABCDE
  • Aim for SpO2 94-98% with oxygen as needed, ABG if
  • sats <92%
  • 5mg nebulised Salbutamol (can repeat after 15 mins)
  • 40mg oral Prednisolone STAT (IV Hydrocortisone if
  • PO not possible)
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10
Q

severe asthma management

A

same as acute +

  • Nebulised Ipratropium Bromide 500 micrograms
  • Consider neb back to back Salbutamol
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11
Q

life threatening asthma

A

acute + severe +

  • Urgent ITU or anaesthetist assessment
  • Urgent portable CXR
  • IV Aminophylline
  • Consider IV Salbutamol if nebulised route ineffective
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12
Q

pneumonia

A

Consolidation on CXR with fever +/- purulent sputum +/ raised WCC and / or CRP

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13
Q

management of pneumonia

A
  • ABCDE
  • If any features of sepsis – immediately treat using sepsis pathway – NO DELAY in initiating IV antibiotics and fluids
  • Otherwise treat with antibiotics as per CURB-65 score, local pneumonia guidelines and awareness of any patient drug allergies
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14
Q

first line Abx for pneumonia

A

PO amoxicillin

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15
Q

second line antibiotics for CAP

A

PO amoxicillin and doxycycline (dual)

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16
Q

third line antibiotics for CAP

A

IV CO-AMOXICLAV or meropenem + oral doxycycline

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17
Q

which pathogens cause typical CAP

A
  • S.pneumoniae
  • H. influenzae
  • S. aureus
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18
Q

which pathogens cause atypical CAP

A

Mycoplasma pneumoniae, Chlamydia pneumoniae, and Legionella pneumophila

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19
Q

common HAPs

A
  • MRSA
  • SA
  • Pseudomonas
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20
Q

masisve haemoptysis

A
  • >240mls in 24 hours OR
  • >100mls / day over consecutive days
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21
Q

Management of Massive Haemoptysis

A

• ABCDE

  • Lie patient on side of suspected lesion (if known)
  • Oral Tranexamic Acid for 5 days or IV
  • Stop NSAID’s / aspirin / anticoagulants
  • Antibiotics if any evidence of respiratory tract infection
  • Consider Vitamin K/
  • CT aortogram – interventional radiologist may be able to undertake bronchial artery embolisation
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22
Q

presentation of tension pneumo

A
  • Hypotension
  • Tachycardia
  • deviation of the trachea away from the side of the pneumothorax
  • mediastinal shift away from pneumothorax
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23
Q

Management of Tension Pneumothorax:

A
  • Large bore intravenous cannula into 2nd ICS MCL
  • Chest drain into the affected side
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24
Q

symptoms of PE

A
  • Chest pain (pleuritic)
  • SOB
  • Haemoptysis
  • Low cardiac output followed by collapse (if Massive PE)
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25
unprovoked PE
*PE i.e. no obvious risk factor – in these cases consider underlying malignancy or thrombophilia*
26
PE management
* ABCDE * Oxygen if hypoxic * Analgesia if pain * Subcutaneous DOAC (or LMWH if contraindicated) whilst awaiting CTPA * Should be fully anticoagulated once confirmed **diagnosis on CTPA**
27
massive PE management
* hypotension/ imminent cardiac arrest * signs of right heart strain on CT / Echo * Consider thrombolysis with IV alteplase (risk of intracerebral bleed approx. 4%)
28
**Thrombolysis contraindications**
29
how to report a chest x-ray
* intro * quality of film * ABCDE * review areas
30
X-ray intro
* Name and age of patient * Date CXR taken * Type of CXR (e.g. PA or AP, erect or mobile) * **Quality of film**
31
**Quality of film**
* **Rotation** * Medial aspect of each clavicle should equidistant from spinous processes * Spinous processes should be vertically orientated against vertebral bodies * **Inspiration** – 5-6 anterior ribs * **Projection** (not AP or PA) * **Exposure**- left hemidiaphragm should be visible to the spine and vertebrae should be visible behind the heart
32
airway
trachea central, carina, bronchi, hilar structures
33
breathing
lungs, pleura
34
cardiac
heart size and border
35
diaphragm
costophrenic angles - flattened?
36
everything else
soft tissue, bones, tubes, valves, pacemakers, review areas
37
review areas
* the lung apices * the retrocardiac region * behind the diaphragm * the peripheral region of the lungs * the hilar regions
38
how to present a potential diagnosis from an X-ray
e.g. “loss of right costophrenic angle which may be in keeping with a pleural effusion” as opposed to “a right pleural effusion”)
39
descriptive terms x-ray
* Refer to zones * Right Upper, Middle and Lower, * Left Upper, Middle and Lower * Shadowing can be * Complete (whiteout of whole lung field) * Dense / opacification (affecting one or more zones), * Diffuse * Alveolar (cotton wool like appearance)
40
**Cardio thoracic ratio**
(The heart diameter is the shorter white arrow; the thoracic diameter is the longer black arrow. The Heart diameter is over 1⁄2 the thoracic diameter. The Cardio-thoracic ratio is therefore increased = Cardiomegaly.)
41
deviation towards pathology
atelectasis
42
deviation away from pathology
pleural effusion pneumothorax
43
pleural effusion X-ray
44
pneumothorax
45
pneumonia
46
Lung cancer
Cant tell the difference between lung cancer and pneumonia on X-ray
47
which medications causes coughs
ACEi, ARB, B blockers, NSAIDS
48
pneumonia and its risk factors
*Lung inflammation caused by bacterial or viral infection, in which the air sacs fill with pus and may become solid. Inflammation may affect both lungs ( double pneumonia ) or only one ( single pneumonia ).* **Risk factors** Smoking, age\>65, immuno-suppression, exposure to chemicals, and underlying lung disease
49
legionaires disease
s a form of pneumonia, usually caused by Legionella pneumophila. Association with infected water in showers or hot tubs – ask your patient if there is a ***history of recent travel or stay in a air conditioned hotel?*** Associated with higher CURB-65 scores.
50
CXR consolidation differntials
Pneumonia TB (usually uopper lobe) lung cancer lobar collapse haemorrhage
51
causes of non-resolving pneumonia
CHAOS
52
**Pneumonia Follow Up**
* HIV test * Immunoglobulins * Pneumococcal IgG serotypes * Haemophilus influenzae b IgG * Follow up in clinic in 6 weeks with a repeat CXR to ensure resolution
53
COVID-19
* Coronavirus disease (COVID-19) is an infectious disease caused by a newly discovered coronavirus Coronaviruses (CoV) are a large family of viruses that cause illness ranging from the common cold to more serious diseases such as Severe Acute Respiratory Syndrome (SARS-CoV) * SARS-CoV-2 (severe acute respiratory syndrome-related coronavirus 2) is the name of the virus, not the disease that results from it. * Can cause a viral pneumonia
54
which COVID-19 pts require hospitlisation
* hypoxia (below 92%) * lymphopaenia * bilateral, lower zone changes on CXR
55
management of hospitalised COVID-19 patients
* Unwell patients require oxygen supplementation, some going on to CPAP or invasive ventilation * Evidence Base e.g. Dexamethasone (and consider Tocilizumab +/- Remdesivir) * Antibiotics may be needed if suspected superadded bacterial infection
56
prevention of covid 19
vaccination
57
novel therapies for covid-19
given to ‘at risk’ people who have tested positive of COVID-10 Casirivimab/imdevimab, sold under the brand name **REGEN-COV** among others, is a medicine developed by the American biotechnology company Regeneron Pharmaceuticals. It is an artificial "antibody cocktail" designed to produce resistance against the SARS-CoV-2 coronavirus responsible for the COVID-19 pandemic
58
covid chest x-ray
59
TB
A bacterial infection spread through inhaling tiny droplets from the coughs or sneezes of an infected person. * Mycobacterium tuberculosis. * Acid-fast bacilli
60
risk factors of TB
61
clinical features of TB
* Often fever and nocturnal sweats (typically drenching) * Weight loss (weeks – months) * Malaise * **Respiratory TB:** cough ± purulent sputum/ haemoptysis, may also present with pleural effusion * **Non-Respiratory TB:** Skin (erythema nodosum); Lymphadenopathy; Bone/joint; Abdominal; CNS (meningitis); Genitourinary; Miliary (disseminated); Cardiac (pericardial effusion)
62
DD of haemoptysis
63
investigations for TB
*Admit to a side room& start infection control measures (e.g. masks & negative pressure room)* * If productive cough: x3 sputum samples for AAFB (acid-alcohol fast bacilli – acid-fast stain also called Ziehl-Neelsen stain) &TB culture (If no productive cough & pulmonary TB suspected consider bronchoscopy) * Routine bloods (especially LFTs) & include HIV test and vitamin D levels * Consider CT chest if pulmonary TB suspected but clinical features/ CXR not typical
64
If diagnosis between pneumonia and TB not clear
start antibiotics for pneumonia (as per CURB-65) whilst investigating possibility of TB.
65
If patient critically unwell and high likelihood of TB (no time to wait for sputum results)
then start anti-TB therapy AFTER sputum samples sent.
66
why is TB treatment started before TB culture
* TB culture can take 6-8 weeks. So, treatment is often started before a culture confirmed diagnosis can be made. A novel PCR test (Gene Xpert) is available in some centres which can give immediate information regarding drug sensitivities or resistance
67
**Anti-TB therapy (ATT)**
* **Ripe (rifampicin, isoniazid, pyrazinamide, ethambutol for 2 moths follow by R and I for 4 months** * Minimum of 6 moths total * Patients weight important – dose dependent * Check baseline LFTs and monitor * Check visual acuity before giving ethambutol * Compliance is crucial and directly observed therapy sometimes used for patients * Pyridoxine also given (while on isoniazid) as prophylaxis against peripheral neuropathy
68
major side effects of TB treatment rifampicin
hepatitis, orange/red secretions, many drug interactions inc warfarin
69
major side effects of TB treatment isoniazid
hepatitis peripheral neuropathy
70
major side effects of TB treatment pyrazinamide
hepatitis, vomiting
71
major side effects of TB treatment ethambutol
optic neuritis (must do a baseline visual acuity test and LFTs must be monitored closely)
72
bronchiectasis
* Chronic dilatation of one or more bronchi. The bronchi exhibit poor mucus clearance and there is predisposition to recurrent or chronic bacterial infection * **Gold standard diagnostic test = High Resolution CT** * Chronic dilatation of one or more bronchi. The bronchi exhibit poor mucus clearance and there is predisposition to recurrent or chronic bacterial infection * Gold standard diagnostic test = High Resolution CT
73
**Bronchiectasis Causes** *
* Post infective – whooping cough, TB * Immune deficiency – Hypogammaglobulinaemia * Genetic / Mucociliary clearance defects – Cystic fibrosis, primary ciliary dyskinesia, Young’s syndrome (triad of bronchiectasis, sinusitis, and reduced fertility), Kartagener syndrome (triad of bronchiectasis, sinusitits, and situs inversus) * Obstruction – foreign body, tumour, extrinsic lymph node * Toxic insult – gastric aspiration (particularly post lung transplant), inhalation of toxic chemicals/gases * Allergic bronchopulmonary aspergillosis * Secondary immune deficiency – HIV, malignancy * Rheumatoid arthritis * Associations – inflammatory bowel disease; yellow nail syndrome
74
**Blood Tests to try and identify cause in newly diagnosed Bronchiectasis:**
* Immunoglobulin levels * Cystic Fibrosis Genotype * Aspergillus IgE / IgG and Total IgE * HIV test * Rheumatoid Factor * Auto Antibodies * Alpha-1-antitrypsin level
75
**Bronchiectasis Common Organisms**
* Haemophilus influenzae * Pseudomonas aeruginosa * Moraxella catarrhalis * Stenotrophomonas maltophilia * Fungi – aspergillus, candida * Non-tuberculous mycobacteria * Less common - Staphylococcus aureus (think about CF)
76
**Bronchiectasis Management**
1. Treat underlying cause 2. Physiotherapy – mucus / airways clearance 3. Sputum for routine culture as well as nontuberculous mycobacteria 4. 10-14 days antibiotics according to sputum cultures / sensitivities for acute exacerbations (infections): Common 1st line Oral Antibiotics: 5. IV antibiotics for severe infections
77
rare side effect of ciprofloxacin
achilles tendonitis
78
**Long term bronchiectasis treatment**
* Long-term (prophylactic) antibiotics for patients with recurrent infective exacerbations * Supportive – flu / covid vaccines, bronchodilators if required * Pulmonary Rehab – MRC Dyspnoea Score \>3 * Long-term (prophylactic) antibiotics for patients with recurrent infective exacerbations * Supportive – flu / covid vaccines, bronchodilators if required * Pulmonary Rehab – MRC Dyspnoea Score \>3 * Long-term (prophylactic) antibiotics for patients with recurrent infective exacerbations * Supportive – flu / covid vaccines, bronchodilators if required * Pulmonary Rehab – MRC Dyspnoea Score \>3
79
**Bronchiectasis Infective Exacerbations**
* Sometimes patients and clinicians find it difficult to distinguish an acute infection (exacerbation) in patients with bronchiectasis versus their baseline chronic symptoms. Here is a useful definition: * A person with bronchiectasis with a deterioration in 3 or more key symptoms for at least 48 hours: * Cough * Sputum volume and / or consistency * Sputum purulence * Breathlessness and / or exercise tolerance * Fatigue * Haemoptysis
80
signs of bronchiectasis on CT
Signet ring sign ## Footnote with the dilated bronchus representing the “ring” and the adjacent smaller artery representing the “jewel” on the ring.
81
**Allergic bronchopulmonary aspergillosis (ABPA)**
* Caused by aspergillus fumigatus exposure * Aspergillus is a common fungus found indoors and outdoors * ABPA is a combination of types 1 and 3 hypersensitivity reactions following inhalation of fungal spores i.e. it is not a fungal infection * Repeated damage from these immunological reactions leads to bronchiectasis (often upper lobe) * ABPA is seen more in patients with Asthma, Bronchiectasis and Cystic Fibrosis * Diagnosis is made by a combination of symptoms (often dry cough and wheeze) along with positive blood tests (raised Aspergillus IgE level as well as a high Total IgE – these are often accompanied by a high eosinophil level too) * Treatment (steroids) may be required if ongoing symptoms and high Total IgE level
82
**CF Definition**
CF is an autosomal recessive disease leading to mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). This can lead to a multisystem disease (most commonly affecting the respiratory and gastrointestinal systems but can affect any part of the body with CFTR) characterised by thickened secretions.
83
**CF Diagnosis**
One or more of the characteristic phenotypic features - * Or a history of CF in a sibling * Or a positive newborn screening test result And * An increased sweat chloride concentration (\> 60 mmol/l) – SWEAT TEST * Or identification of two CF mutations – genotyping * Or demonstration of abnormal nasal epithelial ion transport (nasal potential difference)
84
**CF Presentations**
* Meconium ileus * In 15-20% of newborn CF infants the bowel is blocked by the sticky secretions. There are signs of intestinal obstruction soon after birth with bilious vomiting, abdominal distension and delay in passing meconium. * Intestinal malabsorption * Over 90% of CF individuals have intestinal malabsorption. In most this is evident in infancy. The main cause is a severe deficiency of pancreatic enzymes. * Recurrent Chest infections * Newborn screening
85
CF complications: resp
* **Respiratory Infections** * Needs aggressive therapy with physio and antibiotics * Antibiotic prophylaxis
86
CF complications: constitutional
* **Low Body Weight** * needs careful monitoring * may be consequence of pancreatic insufficiency (lack of pancreatic enzymes), therefore in those patients give pancreatic enzyme replacement therapy * high calorie intake and often extra supplements - may need NG or PEG feeding
87
CF complications: GI
* **Distal Intestinal Obstruction Syndrome (DIOS)** * DIOS vs. constipation – faecal obstruction in ileocaecum versus whole bowel * Due to intestinal contents in the distal ileum and proximal colon (thick, dehydrated faeces) * Due to insuffiencet prescription of pancreatic enzymes or non compliance, also salt deficiency/ hot weather * Palable right iliac fossa mass (faecal) * **Diagnosis**:right palabale mass in iliac fossa, AXR demonstratingfaecal loading at junction of small and large bowel * **Treatment**: PO Gastrografin–this works by drawing water across the bowel wall by osmosis into the bowel lumen, aiming to rehydrate the dehydrated faecal mass and allow it to pass
88
CF can also be related to
diabetes **the thick, sticky mucus causes scarring of the pancreas**. This scarring prevents the pancreas from producing normal amounts of insulin. So, like people with type 1 diabetes, they become insulin deficient.
89
**CF Lifestyle Advice**
* No smoking * Avoid other CF patients * Avoid friends / relatives with colds / infections * Avoid jacuzzis (pseudomonas) * Clean and dry nebulisers thoroughly * Avoid stables, compost or rotting vegetation – risk of aspergillus fumigatus inhalation * Annual influenza immunisation * Sodium chloride tablets in hot weather / vigorous exercise
90
**CF Management**
* As per bronchiectasis – physio for airways clearance * Exercise * Mucolytic treatment options also include nebulised DNase (pulmozyme) * Pancreatic Enzyme Replacement Therapy (e.g. Creon) for patients who are Pancreatic Insufficient * Nutritional supplementation if under weight * Fat soluble vitamin (A,D,E,K) replacement * Long-term antibiotics (sometimes inhaled or nebulised) * Optimisation of CF related diabetes – this occurs in approximately 1 in 3 adults with CF and if present requires insulin therapy * Novel CFTR modulators / potentiators (e.g. Kaftrio) – these have shown excellent efficacy with improvements in FEV1, weight, quality of life and a reduction in frequency of infective exacerbations * Long-term monitoring for CF related diabetes, CF related liver disease and osteoporosis