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نقش درمان آسپرژیلوس برونکوپولمونری آلرژیک با استفاده از آنتی‌ایمونوگلوبین E (آنتی‐IgE) در افراد مبتلا به فیبروز سیستیک

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Appendices

Appendix 1. Glossary

Term

Explanation

Antigen

Any substance capable of inducing a specific immune response and of reacting with the products of that response.

Cɛ3 domain

One part of IgE antibody.

Cytokine

A non‐antibody protein released by a cell population on contact with a specific antigen.

Eosinophil count

Number of a type of white blood cells.

Eepithelialized

Where skin is present.

Hhyphae

Threadlike structures in a fungus.

Monoclonal anti‐IgE antibody

An antibody against the immunoglobulin E antibody which is produced by a single clone of cells, therefore a single pure type of antibody.

Peripheral blood eosinophilia

An increase in eosinophils (a type of white blood cells) circulating in the blood.

Quasi‐randomized trials

Where method of allocation is not completely random, e.g. alternation, date of birth, day of week or case record number etc.

Appendix 2. Additional electronic search strategies

Database

Date searched

Search terms

Clinicaltrials.gov

(clinicaltrials.gov)

29 September 2017

'anti IgE and cystic fibrosis' AND 'omalizumab and cystic fibrosis'

WHO ICTRP

(apps.who.int/trialsearch/)

24 January 2018

'anti IgE and cystic fibrosis' AND 'omalizumab and cystic fibrosis'

Study flow diagram.
Figuras y tablas -
Figure 1

Study flow diagram.

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figuras y tablas -
Figure 2

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
Figuras y tablas -
Figure 3

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Table 1. Adverse effects in included trial

AEs

Omalizumab group

N = 9, n (%)

Placebo group

N = 5, n (%)

Non‐serious AEs

Participants with AE(s)

9 (100)

5 (100)

Infective pulmonary exacerbation of CF

7 (78)

4 (80)

Cough

4 (44)

1 (20)

Headache

4 (44)

1 (20)

Pyrexia

3 (33)

2 (40)

Hemoptysis (blood in sputum)

4 (44)

0

Injection site swelling

4 (44)

0

Injection site warmth

4 (44)

0

Injection site erythema (redness)

3 (33)

0

Hypokalemia

2 (22)

0

Nasopharyngitis

2 (22)

0

Sputum increased

1 (11)

1 (20)

Bronchopulmonary aspergillosis allergic

2 (22)

0

Rhonchi (noisy expiratory breathing sound)

1 (11)

1 (20)

Non‐cardiac chest pain

1 (11)

1 (20)

Vomiting

0

1 (20)

SAEs

Participants with any SAE

6 (67)

1 (20)

Infective pulmonary exacerbation of CF

5 (56)

1 (20)

Allergic Bronchopulmonary Aspergillosis

2 (22)

0

Distal intestinal obstruction syndrome

1 (11)

0

Hemoptysis

1 (11)

0

Rhonchi

1 (11)

0

AE: adverse event
CF: cystic fibrosis
SAE: serious adverse event

Figuras y tablas -
Table 1. Adverse effects in included trial