2013
DOI: 10.1016/j.pupt.2013.01.011
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Stepping-across controlled asthmatic patients to extrafine beclometasone/formoterol combination

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Cited by 16 publications
(6 citation statements)
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“…The clinical effectiveness of efBDP-FOR in asthma patients requiring combination ICS-LABA therapy is well established. 12–16,21–27,46,47 However, to our knowledge, no studies have evaluated both the clinical and cost effectiveness of switching from another ICS-LABA combination to efBDP-FOR in the typical asthma patient — a scenario that is likely to be increasingly common in primary care, given the substantially lower cost and comparable effectiveness of the efBDP-FOR inhaler and, in the UK, certain NHS recommendations to physicians. 2…”
Section: Discussionmentioning
confidence: 99%
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“…The clinical effectiveness of efBDP-FOR in asthma patients requiring combination ICS-LABA therapy is well established. 12–16,21–27,46,47 However, to our knowledge, no studies have evaluated both the clinical and cost effectiveness of switching from another ICS-LABA combination to efBDP-FOR in the typical asthma patient — a scenario that is likely to be increasingly common in primary care, given the substantially lower cost and comparable effectiveness of the efBDP-FOR inhaler and, in the UK, certain NHS recommendations to physicians. 2…”
Section: Discussionmentioning
confidence: 99%
“…14 In another recent RCT, asthma patients previously controlled with FP-SAL (500μg/day FP) were effectively stepped across or switched to efBDP-FOR (400μg/day efBDP); lung function and asthma control were maintained, no safety issues were reported, and efBDP-FOR was noted to have a relatively rapid (5 min) onset of action. 25 However, those studies involved carefully selected patient populations, as is typical of a RCT, and did not include cost analyses.…”
Section: Discussionmentioning
confidence: 99%
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“…Few studies have evaluated whether asthma control can be maintained when patients are stepped across from one ICS/LABA to another (18,19); therefore, this Phase IIIa study was conducted to evaluate whether FF/VI 100/25 µg OD was non-inferior to FP/SAL 250/50 µg BID in adult and adolescent patients with persistent asthma already well controlled on BID ICS/LABA. The study examined lung function and tolerability, as well as patientreported symptoms and quality of life.…”
Section: Introductionmentioning
confidence: 99%