Publications by authors named "J Ficker"

Background: In patients with chronic diseases, including those with chronic obstructive pulmonary disease (COPD), knowledge on the disease and its self-management is considered as relevant for improving disease control and long-term outcome. We studied to which extent components of knowledge depended on potential predictors, such as participation in educational programs and disease severity. For example, the perception of exacerbations or GOLD grade might modulate the content and reliability of COPD understanding.

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Rationale: Adherence to positive airway pressure (PAP) therapy is a common and challenging issue. Although some studies have looked at the impact of initial mask selection, there is a lack of data regarding the impact of a change in mask on adherence to PAP therapy.

Objective(s): This study investigated the impact of a mask change or renewal on mid-term PAP adherence.

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Article Synopsis
  • The iNAP® Sleep Therapy System effectively reduces the severity of obstructive sleep apnea by applying negative oral pressure through an intra-oral device.
  • In a study involving 130 patients, over half (52%) showed significant improvement with more than 50% reduction in apnea-hypopnea index (AHI) after using the device.
  • The system was well-tolerated with low adverse events, and improvements in oxygen saturation and AHI were maintained even 28 days after treatment.
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Background: Telemonitoring-guided interventions can improve short-term positive airway pressure (PAP) therapy adherence, but long-term effects are unknown. This study investigated long-term PAP therapy termination in patients with sleep apnoea managed with standard care, telemonitoring-guided proactive care or telemonitoring-guided proactive care + patient engagement tool.

Methods: German healthcare provider data were analysed retrospectively.

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Osimertinib has become the preferred first-line therapy for epidermal growth factor receptor ( mutation-positive metastatic non-small cell lung cancer (NSCLC) in recent years. Originally, it was approved for second-line treatment after epidermal growth factor receptor tyrosine kinase inhibitors (TKIs) of the first and second generations had failed and T790M had emerged as a mode of resistance. Osimertinib itself provokes a wide array of on- and off-target molecular alterations that can limit therapeutic success.

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