3. Objectives
Facts
Review of current BTS guidelines
Diagnosing Acute Asthma in ED
Managing Acute Asthma
When to admit/safe discharge
4. UK key Facts
One of the common conditions seen at Emergency
Department (ED) is asthma.
5.4 million people in the UK are currently receiving
treatment for asthma: 1.1 million children (1 in 11) and 4.3
million adults (1 in 12)
Asthma prevalence is thought to have plateaued since the
late 1990s, although the UK still has some of the highest
rates in Europe and on average 3 people a day die from
asthma.
In 2014 (the most recent data available) 1216 people died
from asthma.
The NHS spends around 1 billion a year treating and
caring for people with asthma—NOT COPD
5. Evidence shows people with an asthma action plan are
four times less likely to be admitted to hospital
because of their asthma.
6. Aim in ED
Focus on ED management with emphasis that:
Emergency Medicine is a : “Prevention, Resuscitation,
Stabilization and appropriate disposition”1 to the
appropriate specialty.
Step1. Diagnosis
Step 2. Assess the severity
Step 3. Treatment
Step 4. Assess the response
7. Which aspects of asthmatics history are
important to current exacerbation?
Prior hospitilizations
ICU admissions
Recent ED visits
Current meds
Co-morbid conditions
9. BTS Asthma guidelines
BTS guidelines for asthma
categorizes presentation into severity
and helps guide treatment with
regards to the category
10. BTS - Moderate exacerbation asthma
• increasing symptoms
• PEFR >50-75% best or predicted
• No features of acute severe asthma
11. BTS - Acute severe asthma
Any one of following;
• PEFR 33-50% best or predicted
• respiratory rate ≥25/min
• heart rate ≥110/min
• inability to complete sentences in one breath
12. Life threatening exacerbation of
asthma
Patient with acute severe asthma with any one of
• PEFR <33% best or predicted
• SpO2 <92%
• PaO2 <8 kPa
• normal PaCO2 (4.6-6.0 kPa)
• silent chest/cyanosis/poor respiratory effort
• Arrhythmia/exhaustion/altered conscious level
13. Key objectives of management
Aim:
- To relieve airflow obstruction and
hypoxaemia
- To prevent relapses
Repetitive administration of rapidly acting
bronchodilators.
Early systemic corticosteroids.
Oxygen
Complications - (pneumothorax)
14. Management of Acute Asthma
Assessment
Clinical features
PEFR
Pulse oximetry
Blood gases (ABG)
Chest X-ray
Not routine
Suspected pneumothorax, consolidation, life threatening, failure
to respond, requiring ventilation
15. Initial Assessment and Management
Assess severity
Good
response
Incomplete
response
Poor
response
Inhaled
SABA
History
Physical Exam
Peak flow determination
16. Treatment of Acute Asthma
Bronchodilator therapy
Salbutamol provides rapid, dose-dependent
bronchodilation.
Continuous administration may be more
effective in severe exacerbations.
Ipratropium bromide is an anticholinergic
bronchodilator with a slow onset of action and
peak effectiveness at 60 to 90 minutes.
17. Treatment of Acute Asthma
Corticosteroid therapy
Oral administration of prednisolone is often
equivalent to iv methylprednisolone unless there is
nausea.
Current evidence is insufficient to permit
conclusions about using inhaled corticosteroids in
acute asthma.
For severe exacerbations unresponsive to
Salbutamol and corticosteroid therapy, adjunctive
treatments may be used: iv magnesium sulphate or
heliox.
18. Magnesium Sulphate
Intravenous magnesium now recommended in patients
with life-threatening attacks. Not recommended for
routine use in asthma exacerbations
Currently, the evidence relates to a single dose (2 g over
20 min)
If an intravenous bronchodilator is to be administered,
current evidence favours the use of intravenous
magnesium rather than intravenous b-agonist or
aminophylline.
Nebulized salbutamol administered in isotonic
magnesium sulfate provides greater benefit than if it is
delivered in normal saline (Evidence A) contentious !!!
19. Treatment of Acute Asthma
Heliox
Heliox is a mixture of helium and oxygen
(usually a 70:30 helium to oxygen ratio) that
is less viscous than ambient air.
Heliox improves delivery and deposition of
nebulized salbutamol.
20. Moderate
PEF >50-75%
SpO2 >92%
No features of severe
Acute Severe
PEF 33-50%
RR >25
SpO2 >92%
HR >110
Cannot complete
sentences
Life threatening
33-92-CHEST
PEF <33%
SpO2 <92%
Cyanosis/Confusion,
Hypotension,
Exhaustion, Silent chest,
Tachycardia
Senior help (ITU,
anaesthetics)
O SHIT!
•O2 to maintain sats 94-98%
•Salbutamol 5mg via O2 driven nebs
•Hydrocortisone IV/oral prednisolone
•Ipratropium via O2 driven nebs
•Consider Magnesium Sulphate IV
ABG, CXR
Salbutamol 4 puffs, then 2
puffs every 2 mins
Salbutamol 5mg via O2
driven nebuliser
If life threatening
features present
Repeat salbutamol nebs,
give oral prednisolone 40-
50mg
21. Asthma in ED short stay unit
(CDU)
Emergency short stay units have been used in the
ED worldwide for several decades.
Studies have shown that they:
Reduce length of stay ( Daly S et al; 2003, Rydman RJ et
al 1999 & 1997, Khan SA et al; 1997)
Improve ED efficiency (Bazarin J et al; 1996)
Are cost-effective ( Graff L G et al; 1988), and
Reduce the number of inpatient admissions (Martinez E
et al; 2001).
22. When is it safe to discharge?
Significant improvement in symptoms
Significant improvement in peak flow –
should be at least 75% of predicted /
personal best
24. Conclusions
Asthma is frequently under treated
Use current guidelines to aid diagnosis and help in
acute management
If patients are not responding as you would expect
Is the diagnosis right?
Are they having the appropriate management?
Are psychological or social factors hindering management?
25. References
1] Daly S, Campbell DA, and C. PA, "Short-stay units and observation medicine: a systematic
review," Med. J. Aust, vol. 178, pp. 559-63, 2003.
[2] Bazarin J, Schneider S, Newman V, and Chodosh J, "Do admitted patients held in the
emergency department impact the through-put of treat and release patients.," Acad. Emerg. Med,
vol. 3, pp. 1113-18, 1996.
[3] Martinez E, Reily BM, Evan AT, and Roberts RR, "The observation unit: a new interface
between inpatient and outpatient care.," Am. J. Med, vol. 110, pp. 274-7, 2001.