Taema OSIRIS 2: Versatile Ventilator for Adult and Pediatric Patients in Emergency and Post-operative Care
The Taema OSIRIS 2 is a versatile medical device designed to cater to a wide range of applications in both adult and pediatric patients. Whether it's in emergency situations, during transportation, inter-hospital transfers, or post-operative recovery, the OSIRIS 2 delivers reliable ventilation support to meet diverse clinical needs. Its adaptability across different scenarios makes it a valuable asset in various healthcare settings, providing essential respiratory assistance when required.
Equipped with multiple ventilation modes, the OSIRIS 2 offers flexibility in treatment approaches. It can deliver Controlled Mechanical Ventilation or Assist Controlled Mechanical Ventilation, allowing healthcare professionals to customize ventilation parameters based on patient condition and requirements. Additionally, clinicians have the option to administer ventilation using either pure oxygen or a mixture of air and oxygen, further enhancing treatment adaptability and patient care.
One notable feature of the OSIRIS 2 is its capability to provide Spontaneous Ventilation with Pressure Support and Positive End-Expiratory Pressure (PEEP). This mode allows for non-invasive ventilation using a mask, offering a more comfortable and less intrusive method of respiratory support. Moreover, this mode operates within a controlled pressure safety framework, ensuring patient safety and optimal ventilation management.
To guarantee continuous and adequate ventilation, even in the absence of spontaneous patient respiration, the OSIRIS 2 incorporates a minimum respiratory rate setting. This proactive measure ensures that ventilation is maintained at a sufficient level, providing assurance to healthcare providers and optimizing patient outcomes. By offering a comprehensive range of ventilation modes and safety features, the OSIRIS 2 emerges as a reliable and versatile solution for respiratory care across various clinical settings.
The Taema OSIRIS 2 provides precise control over various ventilation parameters, allowing healthcare professionals to tailor treatment to individual patient needs. With adjustable settings for tidal volume, respiratory rate, PEEP, inspiratory trigger, I:E ratio, and FiO2, clinicians have the flexibility to optimize ventilation therapy based on patient condition and response. Tidal volume can be adjusted within a range of 100 to 1500 mL, while respiratory rate settings range from 6 to 40 breaths per minute, ensuring customizable ventilation rates to suit diverse patient requirements.
Additionally, the OSIRIS 2 offers control over Positive End-Expiratory Pressure (PEEP), with settings ranging from 0 to 15 cmH2O. This feature helps maintain lung recruitment and improve oxygenation by preventing alveolar collapse during expiration. The inspiratory trigger can be adjusted within a range of -0.5 to -4 cmH2O, facilitating responsive ventilator triggering based on patient effort.
The device also allows for adjustment of the I:E ratio, ranging from 1:3 to 1:1, enabling clinicians to fine-tune the balance between inspiration and expiration for optimal gas exchange. Furthermore, FiO2 settings can be adjusted to deliver 100% oxygen or a mixture of air and oxygen, providing flexibility in oxygen therapy delivery.
In CMV-ACMV mode, the OSIRIS 2 can deliver ventilation with either 100% oxygen or an air/oxygen mixture, accommodating various clinical scenarios and patient needs. Pressure Support mode offers additional support by delivering pressures ranging from 5 to 40 cmH2O, ensuring adequate ventilation assistance while allowing for patient comfort and synchrony.
The OSIRIS 2 is equipped with comprehensive alarm systems, including audible and visual alarms with a liquid-crystal display for alarm messages. Alarms can alert healthcare providers to critical parameters such as maximum and minimum airway pressures (Pmax and Pmin), maximum respiratory rate (fmax), and power supply status. These alarms help ensure patient safety and enable timely intervention in the event of deviations from preset ventilation parameters, enhancing the overall monitoring and management of ventilated patients.
