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Synchrony

Manufactured by Philips
Sourced in Germany

Synchrony is a high-performance lab equipment product from Philips. It is designed for precise and reliable data collection and analysis. The core function of Synchrony is to synchronize and integrate multiple data sources, enabling researchers to obtain comprehensive and synchronized data for their experiments and studies. Synchrony is an essential tool for a wide range of laboratory applications, providing researchers with the necessary capabilities to conduct their work efficiently and effectively.

Automatically generated - may contain errors

2 protocols using synchrony

1

High-Flow Nasal Cannula vs. Non-Invasive Ventilation

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HFNC was delivered using an Optiflow nasal interface connected to the PT101AZ (Airvo2) humidifier (Fisher & Paykel Healthcare, Auckland, New Zealand). Therapy typically was initiated at a flow of 35 L/min, titrating flow upward if tolerated to 45–50 L/min, in order to maintain SaO2 > 90% or according to specific clinical orders. In addition, all patients from the HFNC group answered a questionnaire about comfort and tolerability during the first 12 h of their admission to the ED.
NIV was initiated by bi-level positive airway pressure (BiPAP) in the spontaneous/timed mode (Synchrony, Respironics, Inc, Murrysville, Pennsylvania) supplied with an identical set of masks. Expiratory and inspiratory pressures were gradually increased to the maximum tolerated over 1 h, in order to maintain SaO2 > 90%, or according to specific clinical orders.
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2

Pressure Support Ventilation in Patients

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Patients were ventilated using the pressure support ventilation (PSV) module of two ventilators (Neftis; Linde, Munich Germany or Synchrony; Philips Respironics, Andover MA, USA).
Inspiratory positive airway pressure (IPAP) was set as the maximum inspiration pressure value tolerated by patients, able to ensure an exhaled tidal volume of 6 mL/kg (measured body weight). Expiratory positive airway pressure (EPAP) between 2 and 8 cmH2O was applied. A back up respiratory rate of 12 breaths/min was set. Oxygen was added to ventilator at a flow able to reach a target SaO2≥ 90%. PSV was delivered using either nasal or full face mask based on patient comfort.
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