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Pb980

Manufactured by Medtronic
Sourced in United States

The PB980 is a lab equipment product manufactured by Medtronic. It serves as a piece of lab equipment with a core function, but no further details about its intended use can be provided in an unbiased and factual manner.

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5 protocols using pb980

1

Invasive Ventilation Protocol for Adults

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We assessed adult patients within 24 h after receiving invasive mechanical ventilation, which was anticipated to be continued for more than 48 h. The exclusion criteria were as follows: patients aged below 18 years, with trauma or chest tube insertion at the measurement point, receiving treatment with continuous neuromuscular blocking agent (NMBA) infusion, and diagnosed with esophageal disease.
Throughout the study period, all patients received pressure assist-control ventilation using the same ICU ventilator (PB840 or PB980) (Covidien, Mansfield, Massachusetts). The inspiratory pressure was set to obtain a tidal volume of 6–8 mL/kg ideal body weight. Parameters such as positive end-expiratory pressure, fraction of inspired oxygen, respiratory frequency, inspiratory time and flow trigger sensitivity were adjusted by bedside physicians. Other patient management strategies were performed by the bedside physicians and nurses according to the critical care guidelines and the analgesia-sedation protocol of our institution.
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2

Comparative Analysis of ICU Ventilators

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Five all-age ICU ventilators (Servo-i [Maquet, Wayne, New Jersey], PB840 [Covidien, Mansfield, Massachusetts], PB980 [Covidien], Evita Infinity V500 [Dra ¨ger, Lu ¨beck, Germany], and Avea [CareFusion, San Diego, California]) (Table 1) were compared, using an ASL 5000 lung simulator (version 3.5, IngMar Medical, Pittsburgh, Pennsylvania) with increasing and decreasing system leaks. Different gas leaks were created by sets of 3-way stopcocks (Discofix, B. Braun Medical, Bethlehem, Pennsylvania) placed between an endotracheal tube/nasal cannula and the lung simulator (Fig. 1). Each ventilator was connected to the lung simulator by a standard neonatal corrugated circuit (Neonatal Breathing Circuit, Hudson RCI-Teleflex, Morrisville, North Carolina). All of the ventilators were studied with a dry circuit.
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3

Comparative Evaluation of ICU Ventilators

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Four all-age ICU ventilators (Servo-i [Maquet, Wayne, New Jersey], PB980 [Covidien, Mansfield, Massachusetts], Evita Infinity V500 [Dra ¨ger, Telford, Pennsylvania], and Avea [CareFusion, San Diego, California]) (Table 1) were compared using an ASL 5000 lung simulator (version 3.5, IngMar Medical, Pittsburgh, Pennsylvania) with increasing and decreasing system leaks. Three-way stopcocks (Discofix, B. Braun Medical, Bethlehem, Pennsylvania) placed between an ETT and the lung simulator were used to create different leak levels (Fig. 1). The connection between the lung simulator and each ventilator was via the manufacturer's standard neonatal circuit or a standard neonatal circuit (Neonatal Breathing Circuit, Hudson RCI-Teleflex, Morrisville, North Carolina). Ventilators were studied with a dry circuit.
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4

Ventilator Performance Evaluation in ICU

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The study was performed in the medical ICU at Hospital Edouard Herriot in Lyon, France. The experimental setup consisted of the following components. An ASL 5000 test lung (Ingmar Medical, Pittsburgh, Pennsylvania) was set in passive condition with a compliance of 20 mL/cm H 2 O to generate high peak expiratory flow and a linear resistance of 5 cm H 2 O/L/s during both inspiration and expiration. Flow and pressure (P ev ) were measured proximal to the expiratory valve (Fig. 1). Air flow was measured with a pneumotachograph (3700 series, Hans Rudolph, Shawnee, Kansas). P ev was assessed with a pressure transducer (Gabarith PMSET 1DT-XX, Becton Dickinson, Singapore). Analog signals of flow and P ev were sent to a data logger (MP150, Biopac, Goleta, California) (Fig. 1). A wireless dual limb ventilator circuit (22 mm inner diameter, 1.6 m long; Intersurgical, Berkshire, United Kingdom) was used. Seven ICU ventilators provided by the French representatives of the manufacturers were tested: PB980 (Medtronic, Dublin, Ireland); C5 and C6 (Nihon Kohden Europe, Roshbach, Germany); Carescape860 (GE Health Care, Chicago, Illinois); Evita V500 (Dra ¨ger, Lu ¨beck, Germany); Servo U ventilator (Maquet-Getinge, Getinge, Sweden); and Respironics V680 (Philips, Amsterdam, The Netherlands).
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5

Ventilator Expiratory Pause Accuracy

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Three ventilators capable of imposing an expiratory pause (negative inspiratory force or negative inspiratory force maneuver) were studied: Evita XL (Dr€ ager, Telford, Pennsylvania), PB-980 (Medtronic, Minneapolis, Minnesota), and Avea (CareFusion, Yorba Linda, California). Each ventilator first underwent a full device check. Expiratory pause maneuver accuracy was tested in 4 modes: CPAP, pressure-support ventilation (PSV), volume control ventilation, and pressure-regulated volume control. CPAP was tested at 5 cm H 2 O and PSV was tested at driving pressures of 10 and 15 cm H 2 O above a PEEP of 5 cm H 2 O. For both volume control ventilation and pressure-regulated volume control, the settings were as follows: f of 20 breaths/min, tidal volume of 500 mL, inspiratory time of 0.85 s, and a PEEP of 5 cm H 2 O. For PSV, a maximum (quickest) pressurization rate was used except for the protocol that examined post-trigger pressurization characteristics. For all protocols (except one that examined the influence of a trigger mechanism and sensitivity level), flow trigger was used and set to a sensitivity of 2 L/min.
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