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Allergic bronchopulmonary aspergillosis in patients with cystic fibrosis
Allergic bronchopulmonary aspergillosis (ABPA) is a pulmonary disorder that often occurs in patients with asthma or cystic fibrosis (CF) and is characterized by a hypersensitivity response to the allergens of the fungus . In patients with CF, growth of hyphae within the bronchial lumen triggers an i...
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Published in: | Annals of thoracic medicine 2017-04, Vol.12 (2), p.74-82 |
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description | Allergic bronchopulmonary aspergillosis (ABPA) is a pulmonary disorder that often occurs in patients with asthma or cystic fibrosis (CF) and is characterized by a hypersensitivity response to the allergens of the fungus
. In patients with CF, growth of
hyphae within the bronchial lumen triggers an immunoglobulin E (IgE)-mediated hypersensitivity response that results in airway inflammation, bronchospasm, and bronchiectasis. In most published studies, the prevalence of ABPA is about 8.9% in patients with CF. Since the clinical features of this condition overlap significantly with that of CF, ABPA is challenging to diagnose and remains underdiagnosed in many patients. Diagnosis of ABPA in CF patients should be sought in those with evidence of clinical and radiologic deterioration that is not attributable to another etiology, a markedly elevated total serum IgE level (while off steroid therapy) and evidence of
sensitization. Management of ABPA involves the use of systemic steroids to reduce inflammation and modulate the immune response. In patients who do not respond to steroids or cannot tolerate them, antifungal agents should be used to reduce the burden of
allergens. Recent studies suggest that omalizumab may be an effective option to reduce the frequency of ABPA exacerbations in patients with CF. Further randomized controlled trials are needed to better establish the efficacy of omalizumab in managing patients with CF and ABPA. |
doi_str_mv | 10.4103/atm.ATM_231_16 |
format | article |
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. In patients with CF, growth of
hyphae within the bronchial lumen triggers an immunoglobulin E (IgE)-mediated hypersensitivity response that results in airway inflammation, bronchospasm, and bronchiectasis. In most published studies, the prevalence of ABPA is about 8.9% in patients with CF. Since the clinical features of this condition overlap significantly with that of CF, ABPA is challenging to diagnose and remains underdiagnosed in many patients. Diagnosis of ABPA in CF patients should be sought in those with evidence of clinical and radiologic deterioration that is not attributable to another etiology, a markedly elevated total serum IgE level (while off steroid therapy) and evidence of
sensitization. Management of ABPA involves the use of systemic steroids to reduce inflammation and modulate the immune response. In patients who do not respond to steroids or cannot tolerate them, antifungal agents should be used to reduce the burden of
allergens. Recent studies suggest that omalizumab may be an effective option to reduce the frequency of ABPA exacerbations in patients with CF. Further randomized controlled trials are needed to better establish the efficacy of omalizumab in managing patients with CF and ABPA.</description><identifier>ISSN: 1817-1737</identifier><identifier>EISSN: 1998-3557</identifier><identifier>DOI: 10.4103/atm.ATM_231_16</identifier><identifier>PMID: 28469716</identifier><language>eng</language><publisher>India: Medknow Publications and Media Pvt. Ltd</publisher><subject>Allergic bronchopulmonary aspergillosis ; allergic fungal mycosis ; Allergies ; Allergy ; Aspergillosis ; Asthma ; Care and treatment ; Cystic fibrosis ; Development and progression ; Epidemiology ; Estimates ; Fungal infections ; Immunoglobulins ; Monoclonal antibodies ; Pathogenesis ; Pediatrics ; Physiological aspects ; Review ; Tuberculosis</subject><ispartof>Annals of thoracic medicine, 2017-04, Vol.12 (2), p.74-82</ispartof><rights>COPYRIGHT 2017 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications & Media Pvt. Ltd. Apr/Jun 2017</rights><rights>Copyright: © 2017 Annals of Thoracic Medicine 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c589t-d142429b8cd7d298fb2dea1b46e320fcc5d458cc080b02fe6bb7c5ce9234b0c93</citedby><cites>FETCH-LOGICAL-c589t-d142429b8cd7d298fb2dea1b46e320fcc5d458cc080b02fe6bb7c5ce9234b0c93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399694/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1903893067?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28469716$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Janahi, Ibrahim Ahmed</creatorcontrib><creatorcontrib>Rehman, Abdul</creatorcontrib><creatorcontrib>Al-Naimi, Amal Rashid</creatorcontrib><title>Allergic bronchopulmonary aspergillosis in patients with cystic fibrosis</title><title>Annals of thoracic medicine</title><addtitle>Ann Thorac Med</addtitle><description>Allergic bronchopulmonary aspergillosis (ABPA) is a pulmonary disorder that often occurs in patients with asthma or cystic fibrosis (CF) and is characterized by a hypersensitivity response to the allergens of the fungus
. In patients with CF, growth of
hyphae within the bronchial lumen triggers an immunoglobulin E (IgE)-mediated hypersensitivity response that results in airway inflammation, bronchospasm, and bronchiectasis. In most published studies, the prevalence of ABPA is about 8.9% in patients with CF. Since the clinical features of this condition overlap significantly with that of CF, ABPA is challenging to diagnose and remains underdiagnosed in many patients. Diagnosis of ABPA in CF patients should be sought in those with evidence of clinical and radiologic deterioration that is not attributable to another etiology, a markedly elevated total serum IgE level (while off steroid therapy) and evidence of
sensitization. Management of ABPA involves the use of systemic steroids to reduce inflammation and modulate the immune response. In patients who do not respond to steroids or cannot tolerate them, antifungal agents should be used to reduce the burden of
allergens. Recent studies suggest that omalizumab may be an effective option to reduce the frequency of ABPA exacerbations in patients with CF. Further randomized controlled trials are needed to better establish the efficacy of omalizumab in managing patients with CF and ABPA.</description><subject>Allergic bronchopulmonary aspergillosis</subject><subject>allergic fungal mycosis</subject><subject>Allergies</subject><subject>Allergy</subject><subject>Aspergillosis</subject><subject>Asthma</subject><subject>Care and treatment</subject><subject>Cystic fibrosis</subject><subject>Development and progression</subject><subject>Epidemiology</subject><subject>Estimates</subject><subject>Fungal infections</subject><subject>Immunoglobulins</subject><subject>Monoclonal antibodies</subject><subject>Pathogenesis</subject><subject>Pediatrics</subject><subject>Physiological aspects</subject><subject>Review</subject><subject>Tuberculosis</subject><issn>1817-1737</issn><issn>1998-3557</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kk1v1DAQhiMEoqVw5YgiceGSxd8fF6RVBbRSEZdytmzHznrlxMFOQP33eGlpWVQhH2yNn3k983qa5jUEGwIBfq-XcbO9_qIQhgqyJ80plFJ0mFL-tJ4F5B3kmJ80L0rZA0AZwfx5c4IEYZJDdtpcbGN0eQi2NTlNdpfmNY5p0vmm1WU-3MSYSihtmNpZL8FNS2l_hmXX2puy1DQfamIFXjbPvI7Fvbrbz5pvnz5en190V18_X55vrzpLhVy6HhJEkDTC9rxHUniDeqehIcxhBLy1tCdUWAsEMAB5x4zhllonESYGWInPmstb3T7pvZpzGGutKumgfgdSHpTOtbDoFMAM9x5g6i0gAlCDBULYIUAdBhQetD7cas2rGV1va3NZxyPR45sp7NSQfiiKpWSSVIF3dwI5fV9dWdQYinUx6smltSgoJEWcEcQq-vYfdJ_WPFWrFJQAC4kB4w_UoGsDYfKpvmsPompLJKiuAIwr1T1CDW5ytcg0OR9q-IjfPMLX1bsx2P8l2Pq3JTt_7wkE6jB3qs6depi7mvDmbyfv8T-Dhn8BSCzTUA</recordid><startdate>20170401</startdate><enddate>20170401</enddate><creator>Janahi, Ibrahim Ahmed</creator><creator>Rehman, Abdul</creator><creator>Al-Naimi, Amal Rashid</creator><general>Medknow Publications and Media Pvt. 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. In patients with CF, growth of
hyphae within the bronchial lumen triggers an immunoglobulin E (IgE)-mediated hypersensitivity response that results in airway inflammation, bronchospasm, and bronchiectasis. In most published studies, the prevalence of ABPA is about 8.9% in patients with CF. Since the clinical features of this condition overlap significantly with that of CF, ABPA is challenging to diagnose and remains underdiagnosed in many patients. Diagnosis of ABPA in CF patients should be sought in those with evidence of clinical and radiologic deterioration that is not attributable to another etiology, a markedly elevated total serum IgE level (while off steroid therapy) and evidence of
sensitization. Management of ABPA involves the use of systemic steroids to reduce inflammation and modulate the immune response. In patients who do not respond to steroids or cannot tolerate them, antifungal agents should be used to reduce the burden of
allergens. Recent studies suggest that omalizumab may be an effective option to reduce the frequency of ABPA exacerbations in patients with CF. Further randomized controlled trials are needed to better establish the efficacy of omalizumab in managing patients with CF and ABPA.</abstract><cop>India</cop><pub>Medknow Publications and Media Pvt. Ltd</pub><pmid>28469716</pmid><doi>10.4103/atm.ATM_231_16</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Allergic bronchopulmonary aspergillosis allergic fungal mycosis Allergies Allergy Aspergillosis Asthma Care and treatment Cystic fibrosis Development and progression Epidemiology Estimates Fungal infections Immunoglobulins Monoclonal antibodies Pathogenesis Pediatrics Physiological aspects Review Tuberculosis |
title | Allergic bronchopulmonary aspergillosis in patients with cystic fibrosis |
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