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The ResMed Lumis 150 VPAP is a bilevel positive airway pressure device designed for non-invasive ventilatory support. It is used in both clinical and home settings, and buyers ranging from hospital procurement teams to informed individual patients need to assess it carefully before ordering. This guide covers the key features, specifications, compatibility considerations and practical limitations worth understanding before purchase.
Unlike a standard CPAP device, the Lumis 150 VPAP delivers two distinct pressure levels: a higher inspiratory pressure and a lower expiratory pressure. This bilevel approach is suited to breathing patterns that require more active ventilatory support throughout the night. The device offers multiple therapy modes, including S, ST and T modes, which determine how the device responds to the patient's own breathing effort.
Understanding which mode is prescribed is essential before ordering. A device supplied in one default mode may require clinical configuration before use. Confirm with the prescribing clinician which mode is required and whether the device has been set accordingly.
The Lumis 150 VPAP includes an iVAPS (intelligent Volume-Assured Pressure Support) mode. This mode automatically adjusts pressure support in response to measured ventilation, targeting a set alveolar ventilation rate. It is a clinically significant feature that distinguishes the 150 series from simpler bilevel devices. If iVAPS is required, verify it is enabled on the specific unit being purchased, as firmware or regional configuration differences can affect mode availability.
The device stores therapy data including leak, tidal volume, respiratory rate and usage hours. This information is accessible via the built-in display and, depending on configuration, through ResMed's AirView remote monitoring platform. Compliance monitoring is a standard requirement in many care pathways. Check whether the device includes wireless connectivity and whether it has been registered to a previous patient account, as this may affect data access.
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ResMed Lumis 150 VPAP ST BIPAP Unit with Power Supply and Bag £539.99 Buy nowView product |
The Lumis 150 VPAP operates across a pressure range suitable for higher-needs patients. Confirm the IPAP and EPAP ranges supported by the unit on offer, as earlier firmware versions may impose different limits. The device includes configurable alarms for apnoea, high leak and disconnection. For clinical or ward use, verify that alarm outputs meet the requirements of the care environment.
The device is compatible with ResMed's HumidAir heated humidifier and ClimateLineAir heated tubing. Humidification reduces the risk of rainout and supports patient comfort throughout the night. The humidifier, water chamber and heated tubing are typically sold separately or as part of a bundle. Confirm what is included with any specific listing before ordering. Standard unheated tubing can be used, but humidification performance will differ.
The Lumis 150 has an integrated power supply and a compact footprint suitable for bedside use. It accepts a standard AC mains supply. There is no internal battery in the standard configuration. If uninterrupted power is required, an external DC power solution or compatible battery pack must be sourced separately. Ask before ordering if power resilience is a requirement.
A pre-owned Lumis 150 VPAP should have its usage hours stated clearly. Hours of use give a practical indication of component wear, particularly on the blower motor. A unit described only as used without an hour count should prompt further enquiry before purchase. Photographs form part of the description on any reputable listing and should show the device exterior, display screen and rear panel clearly.
Any pre-owned unit offered for clinical or patient use should have been cleaned and inspected before dispatch. Function testing should confirm that the device powers on, cycles through modes, generates the correct pressures and displays no active fault codes. A full engineer service and calibration is a separate matter and is not implied by in-house function testing alone. If the care environment requires periodic electrical safety testing under PUWER, this remains the responsibility of the operating organisation.
The Lumis 150 is compatible with a wide range of ResMed and third-party interfaces. However, the device requires a compatible circuit with the correct vent configuration. Single-limb circuits with an integrated leak port or a separate vent valve are both possible depending on the mode in use. Confirm the circuit type required before ordering tubing or a mask. The interface, cushion, headgear and tubing are consumable items and are not typically included with a pre-owned device unless stated.
The following items are frequently omitted from a base device listing and must be sourced independently:
The ResMed Lumis 150 VPAP is a capable bilevel device with advanced ventilation modes including iVAPS. Buyers should confirm the therapy mode required, verify usage hours and function test status on pre-owned units, and establish clearly which accessories are included. Humidification components, tubing, interface and consumables are almost always sold separately. For clinical use, PUWER obligations and any site-specific commissioning requirements remain with the operating organisation. When any detail is uncertain, ask before ordering.
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