Opciones de fuentes de alimentación

Descubra las opciones de fuentes de alimentación de Aerogen 

Controladores Aerogen Pro-X y Aerogen USB: reutilizables, flexibles y portátiles

Descubra el controlador Aerogen Pro-X: una fuente de alimentación de Aerogen

Descubra el controlador Aerogen Pro-X, una fuente de alimentación que alimenta la tecnología Aerogen en cada fase del proceso respiratorio del paciente, incluidas: ventilación mecánica invasiva (VMI), alto flujo (AF), ventilación no invasiva (VMNI) y respiración espontánea (RE). El controlador Aerogen Pro-X es una fuente de alimentación portátil que cuenta con modo continuo y de 30 minutos, desarrollada para facilitar la administración de fármacos en aerosol en todo el hospital.1

Reutilizable

Fácil de configurar, el controlador Aerogen Pro-X se puede utilizar varias veces, en diferentes pacientes, en todo el hospital.1

Flexible

Dos modos de uso, 30 minutos y continuo, según las necesidades de administración de medicación.1

Portátil

Gracias a su batería interna de 45 minutos, podrá llevar el controlador Aerogen Pro-X a donde necesite. Con adaptador opcional de montaje múltiple para un uso más prolongado en una sola ubicación.1


Controlador Aerogen Pro-X

Controlador USB Aerogen

Descubra el controlador USB Aerogen: una fuente de alimentación de Aerogen

Descubra el controlador USB Aerogen, una fuente de alimentación portátil que puede utilizarse a través de la conexión USB y los puertos USB de ventiladores y otros equipos médicos (no disponible en EE. UU.). El controlador USB Aerogen permite elegir entre los modos de funcionamiento de 30 minutos y 6 horas, y alimenta la tecnología Aerogen en cada fase del proceso respiratorio del paciente, incluidas VMI, AF, VMNI y RE. 2

Reutilizable

Fácil de configurar, el controlador USB Aerogen se puede utilizar varias veces, en diferentes pacientes de todo el hospital.2

Flexible

Dos modos de uso, 30 minutos y 6 horas, según las necesidades de administración de medicación.2

Portátil

Permite el funcionamiento desde los puertos USB de los ventiladores o cualquier otro equipo médico (no disponible en EE. UU.), así como el enchufe con opción de adaptador de CA/CC de Aerogen.2

Controladores de Aerogen

Soporte de producto

Aerogen Ultra with a face mask for EMS use: set-up guide

Aerogen Ultra with mouthpiece for EMS use: set-up guide

Aerogen Solo on a NIV single-limb circuit for EMS use: set-up guide

Aerogen Solo on the dry side of the humidifier: set-up guide

Aerogen Solo for adult nasal high-flow: set-up guide

Aerogen Solo for paediatric nasal high-flow: set-up guide

Aerogen Solo at the wye: set-up guide

Aerogen Continuous Nebulisation Tube: set-up guide

Aerogen Ultra: set-up guide

General

I have a medical/clinical query, or my query is not addressed below. Who can I contact for medical or clinical information related to the use of Aerogen products?

Please contact Aerogen Medical Affairs directly for medical information/published clinical research regarding the use of Aerogen products. Email: MedicalScience@aerogen.com (US/Canada/LATAM) or msl@aerogen.com (all other countries).

What medications can be used with the Aerogen Solo, Aerogen Pro?

The Aerogen Solo & Aerogen Pro should be used with physician prescribed medications for inhalation which are approved for use with a general purpose nebuliser.¹ Should you require information on a whether a medication is approved for inhalation please contact the medication manufacturer directly.

Should I adjust the drug dosage when I’m using the Aerogen Solo, Aerogen Pro?

Information on drug dosing must be sourced from the manufacturer’s approved prescribing information for the inhaled formulation. Aerogen Ltd cannot provide specific advice on medication dose.

Is the drug affected if it causes discoloration of the water in a humidifier?

Occasionally, a change in the colour of the water in a heated humidifier has been noted with certain medications if aerosolized proximal to the humidifier. Should you have concerns related to a specific medication please do not hesitate to contact the Medical Affairs team at the email addresses listed above for assistance. The treating clinician should always consider a medications SPC and/or consult with a pharmacist/hospital pharmacy to determine whether placement proximal to the humidifier is suitable for a given therapeutic. Aerogen devices are approved for use in a number of positions offering the treating health care professional a range of placement options if discoloration is a concern. These positions are detailed in the directions for use documents which are accessible on the website.¹

What do I do if crystals form in the nebuliser chamber?

Any medication that has a high ionic concentration, for instance hypertonic saline solutions, if permitted to dry on the Aerogen Vibronic aerosol generator in the nebuliser chamber, may form visible crystals. In the event where crystallisation is observed in the Aerogen Solo, Aerogen recommend to aerosolise a few drops of normal saline solution to clear any residual crystallisation.

How do you remove residue in the chamber after nebulisation of viscous drugs?

Should you wish to remove any viscous drug residues from the Aerogen Solo medication reservoir you may nebulise a few drops of normal saline.

What effect does bias ventilator flow have on aerosol output and deposition?

The impact of bias ventilator flow on aerosol deposition depends on the location of the aerosol generator in the circuit. An in vitro study by Ari et al., (2010) assessing aerosol delivery during mechanical ventilation in the presence of bias flow determined that optimal aerosol deposition may be achieved by nebuliser placement on the dry side of humidifier. Similarly, Berlinski & Willis (2013) demonstrated in a paediatric model, that in the presence of bias flow, nebulisers were more effective when placed back at the humidifier as compared to closer to the wye.²⁻³ In the absence of bias flow optimal deposition was observed when the nebuliser was placed at or close to the wye in this adult model.⁴

Can you use a Heat and Moisture Exchange Device (with filter) (HME/HMEF) while delivering aerosol with the Aerogen Solo?

Yes, the Aerogen Solo is approved for use with a HME.¹ The Aerogen Solo should be placed between the patient and HME as detailed in the Aerogen Solo directions for use.¹ Note: Only a HME/HMEf approved for use with a nebuliser should be used. Follow the HME/HMEf manufacturer instructions regarding use with a nebuliser. Ensure the combination of nebuliser, T-piece and HME/HMEf volumes are suitable for the tidal volume being delivered, according to the patient size.

What are the advantages of Aerogen vibrating mesh nebulisers (VMN) compared with other nebulisers, or inhalers for adult and pediatric patients?

Aerogen vibrating mesh nebulisers are electrically powered, quiet and require no additional flow or pressure to operate, ensure a minimal residual volume and are suitable for use with physician prescribed solutions that are approved for use with a general-purpose nebulisers.¹ A narrative review by Lin et al. compared VMN with other, similar, during invasive mechanical ventilation.⁵

Can you deliver an effective dose with the Aerogen Solo to an adult patient during High flow therapy?

Both in vitro and in vivo studies have examined aerosol delivery efficiency via Aerogen devices concurrent with High Flow Nasal Oxygen therapy with adult models/patients⁶⁻¹⁰ These studies suggest that an effective dose may be delivered during concurrent High Flow Nasal Oxygen therapy and medication aerosolisation via the Aerogen Solo.⁶⁻¹⁰

Do different ventilator parameters affect aerosol delivery?

Yes, a range of ventilator parameters; including flow, inspiratory time (duty cycle), ventilatory mode, timing of nebulisation and circuit features; tube sizes, heat, and humidification, can affect aerosol delivery in mechanically ventilated patients.2,11-13 Reviews by Dr. Dhanani and others summarise the impact of these features on aerosol delivery.11,13

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  1. 30-354 Rev U Aerogen Solo Instruction Manual.
  2. 30-763 Rev H Aerogen USB Controller System Instruction Manual.

GL1222B04-23