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COPD vs BA
GOLD & GINA
Updates in Guidelines
By: Dr Riham Hazem Raafat
Ass. Prof. of Chest Diseases
Ainshams University
1
 70 years old male with a history of dyspnea for 10 years
 Presenting with dyspnea with white productive
sputum, no fever or URI symptoms
 Skin test +ve for house dust mites, pollens, and cockroaches
 Non-smoker
 Is it COPD or Asthma ?
Obstructive Lung Diseases
Integrity and elasticity of lung : DESTROYED
Poor elastic recoil: Air trapping (Hyperinflation)
Problem is with expiration.
Patient has to force the air out using abdominal & intercostal muscles: EXERTION
In Spirometry: FEV1/FVC is decreased.
2
Symptoms
10 %
COPD
have more
reversibility
5% severe
Asthma
usually episodic in
nature, does not
progress, usually
begins in early
childhood, and shows
a good response to
bronchodilators and
corticosteroids
very slowly
progressive onset
and most patients
are diagnosed in
their 60s, there is
little variability in
symptoms, and
patients show a
poor response to
bronchodilators and
corticosteroids
Airflow Limitation
CXR Usually Normal unless?
Abnormal
Usually in > 20 pack years
(Triggers)
Features suggestive of BA or COPD must fulfill at least 3 or more
of the following to settle diagnosis of one of them:
• Age of onset
• Pattern of symptoms
• Lung Function
• Lung Function between attacks
• PH/FH
• Time course
• CXR
GOLD
• Launched in 1997 in collaboration with the NHLBI, NIH and WHO.
• Non-biased review of the current evidence for assessment, diagnosis
and treatment of patients with COPD that can aid the clinician.
Objectives
Recommend effective management and prevention strategies.
Increase awareness among medical community, health officials and the
general public
Decrease morbidity and mortality through implementation of effective
programs
6
Descriptive levels of Evidence
7
Evidence
category
Sources of Evidence
A • RCT with a rich body of data
B • RCT with a limited body of data
• Meta-analysis of RCTs
C • Non-randomized trials
• Observational studies
D • Panel Consensus Judgment
Pathways to Diagnosis
Onset in midlife
Slowly Progressive
© 2019 Global Initiative for Chronic Obstructive Lung Disease
Refined ABCD assessment tool
4
Assessment of Exacerbation Risk
- COPD exacerbations are defined as an acute worsening of respiratory symptoms
that result in additional therapy.
- Classified as:
 Mild (treated with SABDs only)
 Moderate (treated with SABDs plus antibiotics and/or oral corticosteroids)
 Severe (patient requires hospitalization or visits the emergency room). Severe
exacerbations may also be associated with acute respiratory failure.
- Blood eosinophil count may also predict exacerbation rates (in patients treated with
LABA without ICS).
© 2019 Global Initiative for Chronic Obstructive Lung Disease
CAT: COPD Assessment Test
mdcalc.com
cattestonline.com
3
mMRCDS:
Modified Medical Research Council
Dyspnea Scale
Pharmacological
treatment algorithm
5
✓
✓
✓
✓
Non-Pharmacological
- Smoking Cessation
- Pulmonary Rehabilitation
- O2 Therapy / MV
- Vaccination
- Surgical/Bronchoscopic interv.
(Individualized)
High Symp
CAT > 20
Eos >300
Updates in Pharmacotherapy in GOLD 2019
8
Co-suspension technique
• New formulation:
• Drug crystals are suspended in HFAbased propellant
by engineered low-density phospholipid particles.
Ferguson GT, Hickey AJ, Dwivedi S. Co-suspension delivery technology in pressurized metered-dose
inhalers for multi-drug dosing in the treatment of respiratory diseases. Respir Med. 2018 Jan
10
ADVANTAGES
1. Porous particle + drug crystal mixtures remain afloat instead of
sedimenting
2. Prevents flocculation/aggregation of drug particles
3. Decreased DDI/DCI
4. Size: 2-3 um: optimum
5. Low spray velocity HFApropellant: decreased dysphonia
1. LABA+LAMA has greater improvement in quality of life
compared to placebo or its individual bronchodilator
components
Martinez FJ et al., Efficacy and Safety of Glycopyrrolate/Formoterol Metered Dose Inhaler Formulated
Using Co-Suspension Delivery Technology in Patients With COPD. Chest. 2017 Feb 11
LABA+LAMA combination
Martinez FJ et al., Efficacy and Safety of Glycopyrrolate/Formoterol Metered Dose Inhaler Formulated
Using Co-Suspension Delivery Technology in Patients With COPD. Chest. 2017 Feb 12
• Efficacy and safety data from 9 DB-RCTs evaluated GP MDI at doses 0.6 to 144ug and
FF MDI at doses 2.4 to 19.2 ug supported selection on GFF (18/9.6 ug) MDI for Phase III
evaluation
• Time period: 24 weeks
• Patients:
 Age group: 40-80 years
 Moderate to severe COPD
 Can continue OCS, ICS or PDE-4 inhibitors
PINNACLE-1
(2103 pts.)
PINNACLE-2
(1615 pts.)
GFF MDI 526 510
GP MDI 451 439
FF MDI 449 437
Placebo 219 223
Tiotropium* 451 N/A
*Open- label (EMA: Active comparator)
Adm. via DPI
Results: Lung Functions
Martinez FJ et al., Efficacy and Safety of Glycopyrrolate/Formoterol Metered Dose Inhaler Formulated
Using Co-Suspension Delivery Technology in Patients With COPD. Chest. 2017 Feb 13
GFF MDI 126 ml GP MDI 66 ml FF MDI 62 ml
PL MDI -24 ml
TIO 105 ml
GFF MDI 116 ml GP MDI 63 ml FF MDI 61 ml
PL MDI 13 ml
150
91
86
-7
122
137
80
8
82
1º 1º
Results: Treatment difference (1º)
14
Resp. Q’naire (on a scale of 0 to100, with lower scores: better functioning)
Other parameters measured:
1. Average use of Rescue Albuterol (Daily andNighttime)
2. No. of exacerbations
CONCLUSION: IMPROVED EFFICACY, SIMILAR SAFETY PROFILE
Martinez FJ et al., Efficacy and Safety of Glycopyrrolate/Formoterol Metered Dose Inhaler Formulated
Using Co-Suspension Delivery Technology in Patients With COPD. Chest. 2017 Feb
PINNACLE-1 PINNACLE-2
GFF MDI GP MDI FF MDI PL MDI TIO GFF MDI GP MDI FF MDI PL MDI
Change
(Baseline Vs. Wk 24)
- 3.3 -1.0 -2.7 -0.8 -2.6 -3.0 -2.2 -2.3 -1.2
Rx difference
(GFF MDI Vs. Others)
N/A -2.33** -0.64 -2-52* -0.73 N/A -0.78 -0.66 -1.72
2. Double blind RCT reported benefits of single-inhaler triple therapy
compared with ICS/LABA therapy in patients with advanced COPD
Lipson DA et al., FULFIL Trial: Once-Daily Triple Therapy for Patients with Chronic
Obstructive Pulmonary Disease. Am J Respir Crit Care Med. 2017 Aug 15
FULFIL: Lung Function and Quality of Life Assessment in COPD with Closed TripleTherapy
Results
16
24 weeks (ITT) 54 weeks (EXT)
OD triple
therapy#
BD ICS/LABA## Vs. OD triple
therapy#
BD ICS/LABA## Vs.
n 911 899 210 220
Change from
baseline FEV1
142 ml -29 ml p<0.001 126 ml -53 ml p<0.001
Mean change
from baseline
SGRQ score
-6.6 -4.3 p<0.001 -4.6 -1.9 p = 0.065
(Maybe due to small
sample size)
Reduction in
exacerbation rate
N/A
Lipson DA et al., FULFIL Trial: Once-Daily Triple Therapy for Patients with Ch
35% reduction; 95%CI, 14–51; (p=0.002) versus dual
ICS/LABA therapy
ronic Obstructive Pulmonary Disease. Am J
Respir Crit Care Med. 2017Aug
# fluticasone furoate 100/umeclidinium 62.5/vilanterol 25 ug
## budesonide 400/formetrol 12 ug
September 2017: USFDAapproval
Grade D-COPD
Once a day oral inhalation
Enhances patient’s adherence to therapy
and reduces device errors that occur when
patients are using multiple inhalers.
C/I during exacerbation episode
Systemic S/E of steroids +
https://www.fiercepharma.com/pharma/glaxo-wins-fda-nod-for-closed-triple-therapy-
trelegy-ellipta-pegged-as-a-blockbuster
17
FDA approval for first “closed” triple therapy
3- Tiotropium Effect
Improves the effectiveness of PR in increasing
exercise performance (Evidence B)
Exacerbation phenotype
Wedzicha JA, Roflumilast: a review of its use in the treatment of
COPD. International Journal of Chronic Obstructive Pulmonary Disease. 2016 18
4. Beneficial effects of roflumilast have been reported in greater
patients with a prior history of hospitalization for an acute
exacerbation
Martinez FJ, Calverley PM, Goehring UM, Brose M, Fabbri LM, Rabe KF.Effect of roflumilast on exacerbations in
patients with severe chronic obstructive pulmonary disease uncontrolled by combination therapy (REACT): a
multicentre randomised controlled trial. Lancet.2015
19
When Blood Eosinophils < 100 cells/ul
Post-hoc analysis
Rabe KF et al., Effect of roflumilast in patients with severe COPD and a history of hospitalisation. Eur Respir J. 2017 Jul
20
• Chronic Bronchitis patients
• Patients who had previously suffered at least one serious exacerbation
Decreases
Neutrophil chemotactic factor
NF-KB translocation
Increases
IL-10
HDAC 2 expression
Non-selective PDE-4 inhibitors
PDE-4B: anti-inflammatory effects
PDE-4D: vomiting
 Rate of severe exacerbations per patient per
year by history of prior hospitalisation in the
previous year.
Update to Roflumilast
(Daliresp)
2017
2019
21
5. Oral Macrolide for one year in patients prone to exacerbations
reduced the risk of exacerbations compared to usual care in
non current smokers.
Albert RK, Connett J, Bailey WC, et al. Azithromycin for Prevention of Exacerbations of COPD. The New
England journal of medicine. 2011;365(8):689-698. doi:10.1056/NEJMoa1104623.
22
Azithromycin 250 mg/day for one year
Albert RK, Connett J, Bailey WC, et al. Azithromycin for Prevention of Exacerbations of COPD. The New
England journal of medicine. 2011;365(8):689-698. doi:10.1056/NEJMoa1104623.
23
Endpoint Azithromycin Placebo
Median time to first exacerbation (days) 266 days 174 days
SGRQ -2.8 ± 12.1 -0.6 ± 11.4
Group Participants Exacerbations
Azithromycin 558 317 (57%)
Placebo 559 380 (68%)
After 1 year of Macrolide?
2017
2019
24
© 2019 Global Initiative for Chronic Obstructive Lung Disease
GINA
GINA guidelines 2018 27
• Launched in 1993 in collaboration with the NHLBI, NIH and WHO.
Objectives
Increase awareness of asthma
Improve management of asthma
Improve availability and accessibility of effective asthma therapy
Difference from GOLD guidelines
Meta analysis: EvidenceA
GINA 2018 guidelines 28
Stepwise management of Asthma
Mild Moderate
29
KEY CHANGES
ICS should be considered for
patients with mild asthma
(rather than SABAalone)
• Reduces R/O
serious exacerbations.
{Reddel et al., Lancet 2017}
SC Mepolizumab
(anti-IL5 mAB) add-on Rx
for patients with severe
eosinophilic asthma
Anti IL-5
Nair P,Wenzel Set al.; ZONDA Trial Investigators. Oral Glucocorticoid-Sparing Effect of Benralizumab inSevere
Asthma. N Engl J Med. 2017
31
*EosinophilicAsthma
*
Nair P,Wenzel Set al.; ZONDA Trial Investigators. Oral Glucocorticoid-Sparing Effect of
Benralizumab in Severe Asthma. N Engl J Med. 2017 33
Results
Other key updates: GINA 2018
1. New Section added: Perimenstrual (catamenial) asthma
• Asthma worse perimenstrually in ~20% women
• More common in women with high BMI; often have dysmenorrhea and shorter cycles.
• Add-on treatment: OCP and/or LTRA may be helpful
2. New therapy added: HDM-SLIT (house dust mite – sublingual IT) Therapy
• When medication is discontinued, symptoms may recur. This is where allergen immunotherapy
(AIT) comes into play
• Repeated doses of a specific relevant allergen for the treatment of IgE-mediated allergicdisease
3. Evidence A: recommendation against stopping ICS during pregnancy
• Stopping ICS increases the risk of exacerbations in pregnancy
34
36
Have a Nice Day
Thank You

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BA vs COPD.pptx

  • 1. COPD vs BA GOLD & GINA Updates in Guidelines By: Dr Riham Hazem Raafat Ass. Prof. of Chest Diseases Ainshams University 1
  • 2.  70 years old male with a history of dyspnea for 10 years  Presenting with dyspnea with white productive sputum, no fever or URI symptoms  Skin test +ve for house dust mites, pollens, and cockroaches  Non-smoker  Is it COPD or Asthma ?
  • 3. Obstructive Lung Diseases Integrity and elasticity of lung : DESTROYED Poor elastic recoil: Air trapping (Hyperinflation) Problem is with expiration. Patient has to force the air out using abdominal & intercostal muscles: EXERTION In Spirometry: FEV1/FVC is decreased. 2
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  • 7. 10 % COPD have more reversibility 5% severe Asthma usually episodic in nature, does not progress, usually begins in early childhood, and shows a good response to bronchodilators and corticosteroids very slowly progressive onset and most patients are diagnosed in their 60s, there is little variability in symptoms, and patients show a poor response to bronchodilators and corticosteroids Airflow Limitation
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  • 10. CXR Usually Normal unless? Abnormal Usually in > 20 pack years (Triggers)
  • 11. Features suggestive of BA or COPD must fulfill at least 3 or more of the following to settle diagnosis of one of them: • Age of onset • Pattern of symptoms • Lung Function • Lung Function between attacks • PH/FH • Time course • CXR
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  • 14. GOLD • Launched in 1997 in collaboration with the NHLBI, NIH and WHO. • Non-biased review of the current evidence for assessment, diagnosis and treatment of patients with COPD that can aid the clinician. Objectives Recommend effective management and prevention strategies. Increase awareness among medical community, health officials and the general public Decrease morbidity and mortality through implementation of effective programs 6
  • 15. Descriptive levels of Evidence 7 Evidence category Sources of Evidence A • RCT with a rich body of data B • RCT with a limited body of data • Meta-analysis of RCTs C • Non-randomized trials • Observational studies D • Panel Consensus Judgment
  • 16. Pathways to Diagnosis Onset in midlife Slowly Progressive
  • 17. © 2019 Global Initiative for Chronic Obstructive Lung Disease
  • 18.
  • 20. Assessment of Exacerbation Risk - COPD exacerbations are defined as an acute worsening of respiratory symptoms that result in additional therapy. - Classified as:  Mild (treated with SABDs only)  Moderate (treated with SABDs plus antibiotics and/or oral corticosteroids)  Severe (patient requires hospitalization or visits the emergency room). Severe exacerbations may also be associated with acute respiratory failure. - Blood eosinophil count may also predict exacerbation rates (in patients treated with LABA without ICS). © 2019 Global Initiative for Chronic Obstructive Lung Disease
  • 21. CAT: COPD Assessment Test mdcalc.com cattestonline.com 3 mMRCDS: Modified Medical Research Council Dyspnea Scale
  • 22. Pharmacological treatment algorithm 5 ✓ ✓ ✓ ✓ Non-Pharmacological - Smoking Cessation - Pulmonary Rehabilitation - O2 Therapy / MV - Vaccination - Surgical/Bronchoscopic interv. (Individualized) High Symp CAT > 20 Eos >300
  • 23. Updates in Pharmacotherapy in GOLD 2019 8
  • 24. Co-suspension technique • New formulation: • Drug crystals are suspended in HFAbased propellant by engineered low-density phospholipid particles. Ferguson GT, Hickey AJ, Dwivedi S. Co-suspension delivery technology in pressurized metered-dose inhalers for multi-drug dosing in the treatment of respiratory diseases. Respir Med. 2018 Jan 10 ADVANTAGES 1. Porous particle + drug crystal mixtures remain afloat instead of sedimenting 2. Prevents flocculation/aggregation of drug particles 3. Decreased DDI/DCI 4. Size: 2-3 um: optimum 5. Low spray velocity HFApropellant: decreased dysphonia
  • 25. 1. LABA+LAMA has greater improvement in quality of life compared to placebo or its individual bronchodilator components Martinez FJ et al., Efficacy and Safety of Glycopyrrolate/Formoterol Metered Dose Inhaler Formulated Using Co-Suspension Delivery Technology in Patients With COPD. Chest. 2017 Feb 11
  • 26. LABA+LAMA combination Martinez FJ et al., Efficacy and Safety of Glycopyrrolate/Formoterol Metered Dose Inhaler Formulated Using Co-Suspension Delivery Technology in Patients With COPD. Chest. 2017 Feb 12 • Efficacy and safety data from 9 DB-RCTs evaluated GP MDI at doses 0.6 to 144ug and FF MDI at doses 2.4 to 19.2 ug supported selection on GFF (18/9.6 ug) MDI for Phase III evaluation • Time period: 24 weeks • Patients:  Age group: 40-80 years  Moderate to severe COPD  Can continue OCS, ICS or PDE-4 inhibitors PINNACLE-1 (2103 pts.) PINNACLE-2 (1615 pts.) GFF MDI 526 510 GP MDI 451 439 FF MDI 449 437 Placebo 219 223 Tiotropium* 451 N/A *Open- label (EMA: Active comparator) Adm. via DPI
  • 27. Results: Lung Functions Martinez FJ et al., Efficacy and Safety of Glycopyrrolate/Formoterol Metered Dose Inhaler Formulated Using Co-Suspension Delivery Technology in Patients With COPD. Chest. 2017 Feb 13 GFF MDI 126 ml GP MDI 66 ml FF MDI 62 ml PL MDI -24 ml TIO 105 ml GFF MDI 116 ml GP MDI 63 ml FF MDI 61 ml PL MDI 13 ml 150 91 86 -7 122 137 80 8 82 1º 1º
  • 28. Results: Treatment difference (1º) 14 Resp. Q’naire (on a scale of 0 to100, with lower scores: better functioning) Other parameters measured: 1. Average use of Rescue Albuterol (Daily andNighttime) 2. No. of exacerbations CONCLUSION: IMPROVED EFFICACY, SIMILAR SAFETY PROFILE Martinez FJ et al., Efficacy and Safety of Glycopyrrolate/Formoterol Metered Dose Inhaler Formulated Using Co-Suspension Delivery Technology in Patients With COPD. Chest. 2017 Feb PINNACLE-1 PINNACLE-2 GFF MDI GP MDI FF MDI PL MDI TIO GFF MDI GP MDI FF MDI PL MDI Change (Baseline Vs. Wk 24) - 3.3 -1.0 -2.7 -0.8 -2.6 -3.0 -2.2 -2.3 -1.2 Rx difference (GFF MDI Vs. Others) N/A -2.33** -0.64 -2-52* -0.73 N/A -0.78 -0.66 -1.72
  • 29. 2. Double blind RCT reported benefits of single-inhaler triple therapy compared with ICS/LABA therapy in patients with advanced COPD Lipson DA et al., FULFIL Trial: Once-Daily Triple Therapy for Patients with Chronic Obstructive Pulmonary Disease. Am J Respir Crit Care Med. 2017 Aug 15 FULFIL: Lung Function and Quality of Life Assessment in COPD with Closed TripleTherapy
  • 30. Results 16 24 weeks (ITT) 54 weeks (EXT) OD triple therapy# BD ICS/LABA## Vs. OD triple therapy# BD ICS/LABA## Vs. n 911 899 210 220 Change from baseline FEV1 142 ml -29 ml p<0.001 126 ml -53 ml p<0.001 Mean change from baseline SGRQ score -6.6 -4.3 p<0.001 -4.6 -1.9 p = 0.065 (Maybe due to small sample size) Reduction in exacerbation rate N/A Lipson DA et al., FULFIL Trial: Once-Daily Triple Therapy for Patients with Ch 35% reduction; 95%CI, 14–51; (p=0.002) versus dual ICS/LABA therapy ronic Obstructive Pulmonary Disease. Am J Respir Crit Care Med. 2017Aug # fluticasone furoate 100/umeclidinium 62.5/vilanterol 25 ug ## budesonide 400/formetrol 12 ug
  • 31. September 2017: USFDAapproval Grade D-COPD Once a day oral inhalation Enhances patient’s adherence to therapy and reduces device errors that occur when patients are using multiple inhalers. C/I during exacerbation episode Systemic S/E of steroids + https://www.fiercepharma.com/pharma/glaxo-wins-fda-nod-for-closed-triple-therapy- trelegy-ellipta-pegged-as-a-blockbuster 17 FDA approval for first “closed” triple therapy
  • 32. 3- Tiotropium Effect Improves the effectiveness of PR in increasing exercise performance (Evidence B)
  • 33. Exacerbation phenotype Wedzicha JA, Roflumilast: a review of its use in the treatment of COPD. International Journal of Chronic Obstructive Pulmonary Disease. 2016 18
  • 34. 4. Beneficial effects of roflumilast have been reported in greater patients with a prior history of hospitalization for an acute exacerbation Martinez FJ, Calverley PM, Goehring UM, Brose M, Fabbri LM, Rabe KF.Effect of roflumilast on exacerbations in patients with severe chronic obstructive pulmonary disease uncontrolled by combination therapy (REACT): a multicentre randomised controlled trial. Lancet.2015 19 When Blood Eosinophils < 100 cells/ul
  • 35. Post-hoc analysis Rabe KF et al., Effect of roflumilast in patients with severe COPD and a history of hospitalisation. Eur Respir J. 2017 Jul 20 • Chronic Bronchitis patients • Patients who had previously suffered at least one serious exacerbation Decreases Neutrophil chemotactic factor NF-KB translocation Increases IL-10 HDAC 2 expression Non-selective PDE-4 inhibitors PDE-4B: anti-inflammatory effects PDE-4D: vomiting  Rate of severe exacerbations per patient per year by history of prior hospitalisation in the previous year.
  • 37. 5. Oral Macrolide for one year in patients prone to exacerbations reduced the risk of exacerbations compared to usual care in non current smokers. Albert RK, Connett J, Bailey WC, et al. Azithromycin for Prevention of Exacerbations of COPD. The New England journal of medicine. 2011;365(8):689-698. doi:10.1056/NEJMoa1104623. 22
  • 38. Azithromycin 250 mg/day for one year Albert RK, Connett J, Bailey WC, et al. Azithromycin for Prevention of Exacerbations of COPD. The New England journal of medicine. 2011;365(8):689-698. doi:10.1056/NEJMoa1104623. 23 Endpoint Azithromycin Placebo Median time to first exacerbation (days) 266 days 174 days SGRQ -2.8 ± 12.1 -0.6 ± 11.4 Group Participants Exacerbations Azithromycin 558 317 (57%) Placebo 559 380 (68%)
  • 39. After 1 year of Macrolide? 2017 2019 24
  • 40. © 2019 Global Initiative for Chronic Obstructive Lung Disease
  • 41. GINA GINA guidelines 2018 27 • Launched in 1993 in collaboration with the NHLBI, NIH and WHO. Objectives Increase awareness of asthma Improve management of asthma Improve availability and accessibility of effective asthma therapy Difference from GOLD guidelines Meta analysis: EvidenceA
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  • 44. GINA 2018 guidelines 28 Stepwise management of Asthma Mild Moderate
  • 45. 29 KEY CHANGES ICS should be considered for patients with mild asthma (rather than SABAalone) • Reduces R/O serious exacerbations. {Reddel et al., Lancet 2017} SC Mepolizumab (anti-IL5 mAB) add-on Rx for patients with severe eosinophilic asthma
  • 46. Anti IL-5 Nair P,Wenzel Set al.; ZONDA Trial Investigators. Oral Glucocorticoid-Sparing Effect of Benralizumab inSevere Asthma. N Engl J Med. 2017 31 *EosinophilicAsthma *
  • 47. Nair P,Wenzel Set al.; ZONDA Trial Investigators. Oral Glucocorticoid-Sparing Effect of Benralizumab in Severe Asthma. N Engl J Med. 2017 33 Results
  • 48.
  • 49. Other key updates: GINA 2018 1. New Section added: Perimenstrual (catamenial) asthma • Asthma worse perimenstrually in ~20% women • More common in women with high BMI; often have dysmenorrhea and shorter cycles. • Add-on treatment: OCP and/or LTRA may be helpful 2. New therapy added: HDM-SLIT (house dust mite – sublingual IT) Therapy • When medication is discontinued, symptoms may recur. This is where allergen immunotherapy (AIT) comes into play • Repeated doses of a specific relevant allergen for the treatment of IgE-mediated allergicdisease 3. Evidence A: recommendation against stopping ICS during pregnancy • Stopping ICS increases the risk of exacerbations in pregnancy 34
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  • 51. Have a Nice Day Thank You