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Asthma control over 3 years in a real-life study.

Lundbäck, Bo, 1948 (author)
Karolinska Institutet,Gothenburg University,Göteborgs universitet,Krefting Research Centre
Rönmark, Eva, 1953 (author)
Umeå universitet,Gothenburg University,Göteborgs universitet,Krefting Research Centre,Yrkes- och miljömedicin
Lindberg, Anne (author)
Umeå universitet,Lungmedicin
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Jonsson, Ann-Christin (author)
Larsson, Lars-Gunnar (author)
James, Mark (author)
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 (creator_code:org_t)
Elsevier BV, 2009
2009
English.
In: Respiratory medicine. - : Elsevier BV. - 1532-3064 .- 0954-6111. ; 103:3, s. 348-55
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • This was a 3-year "real-life" study, during which patients' medication was increased and decreased to achieve sustained asthma control. Patients (282) were randomised to receive treatment with SAL 50microg, FP 250microg, or SFC 50/250microg via a Diskustrade mark inhaler, bid. A 12-month double-blind period was followed by a 2-year open phase. The physician increased or decreased patients' medication to achieve and maintain asthma control at regular clinical assessments using criteria based on the asthma treatment guidelines. On completion 73% (168/229) of the subjects were receiving SFC to maintain control of their asthma, compared with 21% (49/229) receiving FP and 5% (12/229) receiving SAL. Odds ratio for requiring increased treatment were 2.66 (p=0.002) for patients initially randomised to FP and 9.38 (p<0.0001) SAL, compared with SFC. Time until 25% of patients first required an increase in study medication was 6months for patients initially treated with SAL compared to 12months for FP and 21months for SFC. Symptoms and use of rescue medication improved first, followed rapidly by PEF with the greatest improvements occurring over the first year. Airway hyperresponsiveness continued to improve throughout the study. The majority of patients achieved and maintained control of asthma over a 3-year period with physician-driven medication changes. Patients treated with SFC were more likely to achieve control than patients treated with FP or SAL alone. Continuing improvements in airway hyperresponsiveness indicate the importance of maintaining treatment after clinical control of symptoms and lung function are achieved.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Lungmedicin och allergi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Respiratory Medicine and Allergy (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Arbetsmedicin och miljömedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Occupational Health and Environmental Health (hsv//eng)

Keyword

Adolescent
Adult
Aged
Albuterol
analogs & derivatives
therapeutic use
Androstadienes
therapeutic use
Asthma
drug therapy
physiopathology
Bronchodilator Agents
therapeutic use
Double-Blind Method
Drug Administration Schedule
Drug Therapy
Combination
Family Practice
Female
Follow-Up Studies
Forced Expiratory Volume
drug effects
Humans
Logistic Models
Lung
physiopathology
Male
Middle Aged
Nebulizers and Vaporizers
Treatment Outcome
Young Adult

Publication and Content Type

ref (subject category)
art (subject category)

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