2001
DOI: 10.1016/s1081-1206(10)62494-5
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Risk factors for the persistence of respiratory symptoms in childhood asthma

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Cited by 21 publications
(13 citation statements)
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“…78.43% of the patients were atopic, confirming previous observations on the proportion of atopics to non-atopics among the asthmatic patients [16]. According to Bahceciler et al [17], allergen sensitivity is a risk factor for the persistence of respiratory symptoms. We proved that in non-atopic patients suffering from asthma, the decline in lung function increases, which is in contrast to a study showing the opposite results [18].…”
Section: Discussionsupporting
confidence: 75%
“…78.43% of the patients were atopic, confirming previous observations on the proportion of atopics to non-atopics among the asthmatic patients [16]. According to Bahceciler et al [17], allergen sensitivity is a risk factor for the persistence of respiratory symptoms. We proved that in non-atopic patients suffering from asthma, the decline in lung function increases, which is in contrast to a study showing the opposite results [18].…”
Section: Discussionsupporting
confidence: 75%
“…During maximal expiration, proximal airways contribute mostly to measurements assessed during the early phase of expiration, including FEV1, whereas distal airways are believed to contribute most to the end of expiration [71]. Therefore, FEF25-75% and FEF50% have been suggested to reflect distal airway obstruction and have been used in epidemiological and therapeutic studies involving asthmatic subjects [72][73][74][75]. However, FEF25-75% and FEF50% are highly variable spirometric tests [76].…”
Section: Noninvasive Measurements Spirometry and Plethysmographymentioning
confidence: 99%
“…We had previously evaluated 279 asthmatic children who had been followed up for 3 years at Marmara University Pediatric Allergy and Immunology Division [11]. We randomly selected 100 patients from this previous study subjects but we could reach 74 patients and 62 of them accepted to attend the study.…”
Section: Subjectsmentioning
confidence: 99%
“…At the end of 1 month, the dose was decreased to 400 mcg/day, if an improvement had been achieved. The dose was then tapered during follow-up visits (every 2-3 months) to the lowest dose needed to control symptoms [11].…”
Section: Follow-up and Therapymentioning
confidence: 99%