2015
DOI: 10.1208/s12248-015-9717-9
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Inhalation Devices and Patient Interface: Human Factors

Abstract: The development of any inhalation product that does not consider the patient needs will fail. The needs of the patients must be identified and aligned with engineering options and physical laws to achieve a robust and intuitive-to-use inhaler. A close interaction between development disciplines and real-use evaluations in clinical studies or in human factor studies is suggested. The same holds true when a marketed product needs to be changed. Caution is warranted if an inhaler change leads to a change in the w… Show more

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Cited by 11 publications
(8 citation statements)
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“…Finally perhaps there is room for improved technology, perhaps with new inhalers with smaller particle size, and simpler use and design which could make the airway delivery of medicinals by inhaler devices more reliable and less operator dependent [ 5 , 28 , 31 ].…”
Section: Discussionmentioning
confidence: 99%
“…Finally perhaps there is room for improved technology, perhaps with new inhalers with smaller particle size, and simpler use and design which could make the airway delivery of medicinals by inhaler devices more reliable and less operator dependent [ 5 , 28 , 31 ].…”
Section: Discussionmentioning
confidence: 99%
“…As changes of devices may decrease adherence, it would be useful to measure upfront which inhaler is best suited for a given patient. (32,38,39) This is further emphasized by the measurements performed in healthy volunteers, where the correlation of inhalation parameters was less optimal, especially using inhalers where actuation of device and inhalation needs coordination.…”
Section: Discussionmentioning
confidence: 99%
“…Unfortunately, approximately 22–78% of patients with asthma and COPD and 31–53% of CF patients are poorly adherent to their inhaled medications [ 36 , 37 ]. Errors in inhalation techniques occur in a percentage of 6.8–43.2%, and only 10–52% of physicians are adequately informed regarding proper device use [ 38 , 39 ]. The most common clinically significant errors include incorrect positioning of both the device and the head, failure (i) to insert and pierce the capsule (for the capsule-based DPIs), (ii) to exhale away from the device prior to inhalation, (iii) to hold the breath after inhalation, and (iv) to maintain a forceful and deep inspiration.…”
Section: Limitations Of Currently Available Dpismentioning
confidence: 99%