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AioCare Doctor is a clinically proven professional application for healthcare professionals (i.e. doctors, nurses, respiratory technicians and clinical trial investigators) to diagnose and monitor chronic respiratory diseases such as asthma, COPD, cystic fibrosis (CF), idiopathic pulmonary fibrosis (IPF) by evaluating lung function and patient symptoms in time. It is intended to use with portable spirometer AioCare. We made spirometry easy and accessible to any healthcare professional, regardless if the examination is performed in the office, hospital (bedside testing) or at home. Advanced AI based algorithms assist during the inhale/exhale maneuvers to assure high quality examination and to prevent typical errors during spirometry performed by less experienced patients and operators or without supervision. Quick reporting and automated interpretation of the bronchodilator test make AioCare the most convenient and safe lung function tool. All professional users get free access to the online panel with instant data upload for better management of multiple patients and trends (FEV1, FVC, PEF) overtime browsing. Ultimate features of AioCare Doctor app: - Full-loop test - Measure FEV1, FVC, PEF, FEV1/FVC, FEF25-75 and other... - GLI and ERS reference values - Pulse Oximetry module (medical grade) - ATS/ERS 2019 Standards of Spirometry - Available modes: full-loop spirometry (FVC maneuver), peak flow meter, heart rate. - Bronchodilator test - Multiple patient records - Convenient contact with your Patient via secure chat - Automatic quality check (AI based algorithms) - Export of results to PDF - Share via email - Secure encrypted connection - E-mail support within 48 hours - Fast integration with eCRFs for clinical trial management, analysis and reporting. - Patient app notifications (reminders) for better patient adherence. Coming soon: - Asthma Action Plan - Self-management plan in the event of an exacerbation - Disease Action Plan planned for your patient - Slow vital capacity (SVC maneuver) Note: The application works with a class IIa medical device that meets the medical device (MDD) standards, compliant with ISO 26782: 2009 and ISO 23747: 2015 standards. The device is certified and CE marked by the TUV Nord Accredited Certification Body for medical devices in the European Economic Area. Please use carefully and in accordance with the purpose and territory (EEA/EU) and in accordance with the instructions for use.
