Floton S20 Advanced Non-Invasive Ventilation

Adaptive Triggering  Technology (ATT)  tracks  every  breath and monitors  the different stages   of   the respiration cycle utilizing an Advanced Leak Calculation Algorithm that ensures reduced work  of  breathing (WOB) whilst providing the patient with effective and comfortable treatment.

Curative Medical Inc., USA  introduces new Floton Non-Invasive Bi Level  Positive   Airway Pressure systems for the treatment of Respiratory insufficiency including COPD  and Obstructive Sleep Apnea.

Compact, Lightweight and Quiet the Floton BiLevel Series understands that every breath is different    using the Advanced Adaptive Triggering Technology (ATT) designed to effortlessly synchronize with the natural breathing of the patient.

The New Cutting Edge Technology incorporates the measurement of the pressure directly at the mask level through a specially designed Hose Pipe.

This technology makes it  possible  for accurate leak  management and enhances the sensitivity of the  machine  to  detect  extremely low patient  effort.

Floton ST series ventilators have advanced  modes of BiLevel  Ventilation  including  CPAP, S,  ST,  T, APCV.  The new APCV (Assisted Pressure Control Ventilation) mode  allows the patient to trigger an inspiration  even as it follows  the Time cycle and backup  breath rate decided by the physician.

One of the main reasons for machine fault is the seepage of water from the integrated humidifier into the machine during transport or shifting. In Floton BiLevel Systems, the disconnection of the integrated humidifier connecting pipe isolates the flow generator from the humidifier.

 

Floton Specifications

Pressure Range BiLevel – S20 : 4cmH20 – 20cmH20
Pressure Measurement Mask Pressure
Ramp Time 0-60min adjustable 1min/step
BPM* 5 to 50 Breaths Per Minute
I/E%* 10% to 80%
Ventilation Mode* 2 modes:  SPONTANEOUS AND CPAP
I-Slop 6 levels. From 100msec to 600msec
Expiratory Cycling E-Sens : 6 Levels
Inspiration Triggering I-Sens : 6 Levels, Adaptive Triggering /
Technology (ATT)
Tidal Volume 50 to 3000ml
Noise (10cm H2O )  <28dB (A)
Dimensions 180mm x 210mm x 105mm
Weight 1.2kg (1.55kg with humidifier)
Automatic Altitude Compensation 700hPa ~ 1060hPa
Mask On / Off Detection Automatic Start/Stop on breath detection
Alarms  Power Failure, Low minute ventilation,Low Tidal Volume, Apnea, High Pressure
Power Supply 100-240 VAC, 50/60 Hz, 24DV, 2.5 A max.
Protection against shock / Water ingress Class II, Type B applied part / IPXO
Electromagnetic compatibility EN 60601-1-2
Certification CE 0123
Relative Humidity 10% ~ 93% (Non-condensing)
Humidifier** Heated, Integrated, 250ml, 44 C
Data Recording 365 days of data storage, Respiratory Events,
Trends of Pressure leak and Respiratory Rate.
* : Feature not available in Floton S20** : Humidifier Optional

WheezoMeter State-of-the-Art Wheeze Measuring Device

The WheezoMeter™ analyzes 30 seconds of breath sounds using advanced signal processing algorithms to detect, quantify and objectively document the presence of wheeze and its extent, the WheezeRATE™.

  • The WheezoMeter™ is calibrated and validated as determined by consensus of a panel of experts who evaluated and scored many recordings for presence of wheeze.
  • The WheezoMeter™ uses a cascade of 6 proprietary technologies to “defend” the signals against false detection of ambient noises as wheeze

WheezeRATE™: Proportion of the respiratory cycle duration occupied by wheezing – Tw/Ttot

Acoustic Respiratory Monitoring

The WheezoMeter™ can be used by:

  • Physicians: Pediatricians, GPs, internists, asthma/allergy specialists.
  • Nurses: Emergency, ICU/PICU/NICU, ward, asthma nurses, school nurses.
  • Technicians and Paramedics: Respiratory therapists, EMS personnel, military medics, sports paramedics, occupational health officers.
  • Patients and Caregivers: Under guidance of a healthcare professional.

The WheezoMeter™ design is based on ergonomic humaninterfacing principles as dictated by functional and anatomical requirements in a state-of-the-art attractive form.

  • Facilitates the correct anatomical placement of the device in contact with the trachea at the correct contact force.
  • Provides stable contact with the skin surface for the duration of the test.
  • Isolates the measuring head and sensor from vibrations and tremor of the hand holding the WheezoMeter™.

WheezoMeter™ uses:

  • Obtain a “spot check” measurement of present wheeze activity, any time, any place, as often as needed without any patient effort.
  • Measure WheezeRATE™ before and after administration of a bronchodilator (“pre-post” test).
  • Communicate status of homebound or remote patient to physician or healthcare professional.

Personal WheezoMeter™ Specifications

System Components WheezoMeter™ with embedded Black Fin® processor. Self-contained cushioned built-in silicone-coated PPG Sensor
Carrying case
Sensors PPG Sensor with broad spectrum frequency response, >60 dB dynamic range and superior ambient noise rejection
Software Proprietary KarmelSonix Wheeze Detection algorithms plus comprehensive ambient noise rejection capability.
Capacity Allows scrolling of the last 10 measurements for review
Batteries 2 AA batteries (not included)
Auxiliary Input Infant sensor holder for babies and
toddlers (optional)
Warranty One year limited warranty
WheezoMeter™ is protected by international and US patents 6,168,568; 6,261,238. Specifications are subject to change without prior notice.

PulmoTrack An Innovative New System for Wheeze Identification & Quantification

Asthma is reversible airflow obstruction, associated with a state of increased responsiveness of the tracheobronchial tree to many different stimuli (that do not affect normal individuals).
…Patients experience dyspnea, cough and wheezing as the major complaints.

Tintinalli: Emergency Medicine, American College of Emergency Physicians


PulmoTrack® enables the continuous monitoring of wheeze and cough*.
This easy, quick and noninvasive system provides:

  • Wheeze by wheeze identification
  • Accurate measurement of Wheeze Rate
  • Classification of wheeze as inspiratory or expiratory
  • Respiratory rate and I\E ratio
  • Cough* Counting

WHEEZE RATE: Proportion of the respiratory cycle duration occupied by wheezing – Tw/Ttot

Respiratory Acoustic Monitor

The PulmoTrack® Respiratory Acoustic Monitor can be used for:

  • Bronchodilatation Test: Measurement of
    response to treatment.
  • Bronchoprovocation Test particularly for
    infants or other non-cooperative patients.
  • Performance of physical examination in a pulmonary function testing environment to identify and quantify the presence of wheezing.

The PulmoTrack® Respiratory Acoustic Monitor system consists of two acoustic sensors attached to the skin over the trachea and chest with disposable acoustic insulating adhesive pads, a pneumo graph belt sensor for documenting breathing activity, and an ambient microphone to filter environmental noises.

Wheeze detection is carried out by patented* software using advanced algorithms that apply strict criteria to determine the presence of wheezing, as defined by CORSA (Computerized Respiratory Sound Analysis) guidelines1.

1. Sovijärvi ARA, Dalmasso F, Vanderschoot J, Malmberg LP, Righini G, Stoneman SAT, Definition of terms for application of respiratory sounds.Eur Respir Rev 2000;10:597-610

PulmoTrack® facilitates improved patient management.

  • Minimum patient active effort offers previously unavailable objective pulmonary symptoms documentation in all age groups and continuous overnight monitoring.
  • Precise measurement of wheeze rate provides quantitative patient data.
  • Archivable and retrievable reports over a period of time enable the following of symptom trends.
  • Detailed graphical spectral display and acoustic playback features allow review of specific records for secondary data analysis.

 

PulmoTrack® Specifications

System Components 2-ppg™ Sensors
Respiratory Sensor including belt
Signal conditioning unit
Analog/digital converting unit
Laptop computer
Acoustic adhesive pads
System case
Sensors Piezoelectric, useful range – 75-4000Hz
Adhesive Pads Biocompatible, noise shield
Software KarmelSonix dedicated software
Software Features Data analysis – wheeze detection
Wheeze rate %
Respiratory rate
I:E Ratio
Data archiving & retrieval
Zooming
Audio playback
Printable reports
*PulmoTrack™ is protected by patent numbers: US 6,168,568, US 6,261,238 & EP 0944355. PulmoTrack™ is FDA, CE & TGA cleared.

WHolter Ambulatory Wheeze and Cough Holter

24-Hour Symptoms Recorder in a Patient’s Own Environment

Ever wonder what the patient is experiencing overnight, during exercise, after a meal, at the work place? The WHolter™ is the first ambulatory wheeze and cough 24-hour recorder that can document objectively and quantitatively patients with:

  • Nocturnal Asthma
  • COPD or Chronic Bronchitis
  • Occupational Asthma
  • Chronic Cough
  • Allergies

The WHolterTM is used to continuously determine and provide a detailed report on:

  • WheezeRATETM, wheeze time over total time
  • Inspiratory and Expiratory WheezeRATETM
  • CoughCOUNTTM, number of coughs per minute/hour
  • Respiratory Rate
  • I:E Ratio

WHolterTM: Listens to your patient when you can’t…

 

Ambulatory Monitor

Overnight or 24-hour WHolterTM recording can be used to

  • Document Nocturnal Asthma, assess its severity and provide a clear temporal pattern of overnight wheeze activity
  • Evaluate level of Asthma control and need for Step-up or Step-down of Asthma treatment
  • Evaluate Chronic Cough patients, symptom association (e.g. exposure) and response to treatment
  • Objectively document effect of occupational and environmental (e.g. fragrances) pollutants and allergen

The WHolterTM overnight or 24 hours recorder is prescribed by a physician to assess symptoms, diagnose nocturnal asthma, chronic cough etc. Dispensing the unit, including patient education, correct application of the sensors in the right locations and activation of the recorder is done in a specialized clinic, e.g. PFT Lab, Sleep Lab, Holter (cardiac, hypertension, asthma / allergy specialist) or at the physician’s office/clinic. At the end of24 hours or 8 hours (if only nocturnal WHolter study is indicated) the patient returns the unit, the data is uploaded and sent for analysis and interpretation.


Fig. 1: The WHolter™ WheezeRATE™ overnight record of a 24 years old asthma patient. Note the early-morning wheeze that eventually woke the patient up to administer Albuterol. The overnight average WheezeRATE was 3.7% with 86 minutes (18.6% of the night) with WheezeRATE > 5%.

The WHolterTM consists of a Data Logger recording unit with a 24 hours digital recording capacity to store continuous information from 2 PPG sensors, pneumogram belt and ambient microphone. The WHolterTM is supplied with a Check-in/Checkout software that allows registering a patient when the deviceis dispensed, upload the recorded data to the computer and prepare the unit for the next patient. Data Analysis is performed by the PulmoTrack® software package sold separately, or as part of a PulmoTrack®-WHolter™. Use of ambient microphone for event recording.

The WHolterTM is intended for performing ambulatory lung sounds and respiratory activity recording on those patients who may benefit from such a recording, including, but not limited to, those with complaints of shortness of breath, wheezing, cough, and when there is a need for performing continuous acoustic pulmonary function measurements.

 

24-Hour Symptoms Recorder in a Patient’s Own Environment

 

Technical Specifications

Data logger capacity : BGb digital recorder
Continuous recording for 24 h
Analog input : Two sound contact sensors
Pneumograph belt
Ambient microphone
Data Acquisition : 16-bit, at 8250 samples per second, per
channel
Contact Sensors : Two PPG sensors
Frequency range: 80-2400 Hz
Required Batteries : 2 AA NiMh >2900AH
Rechargeable batteries (not included)
Dimensions and
Weight :
13.8 x 7.6 x 2.6 cm
210 gr (with batteries)
Check-In/Out
Software :
Supplied on a CD, used to login patient
and upload of data
Wholter™ is protected by patents 6,168,568; 6,261,238, and by pending US and international patents. PulmoTrack-CC™, WheezeRATE™, CoughCOUNT™ are trademarked by KarmelSonix.
Specifications are subject to change without prior notice.

OSAScreen Sleep Screener

Fast, Simple and Versatile
OSA Screening, CPAP Pressure Determination
Extensive Reports

OSAScreen is an advanced Medical Device for the screening of Sleep Disordered Breathing (SDB), specially for Obstructive Sleep Apnea Syndrome (OSAS). It records the patient respiratory oral and nasal airflow, snoring, SaO2, Pulse Rate and CPAP pressure.

Highly informative reports are analysed and generated from this collected data.

Advanced Ergonomic Design

  • Wrist worn, light weight and low power consumption.
  • 2-inch Coloured LED, displays all parameters and waves in real time.
  • Icon operation, recording length and Battery indication.
  • 24 hours embedded recording capacity, Micro-SD and Bluetooth optional.

Powerful Device for SDB

  • Records 7 parameters: SpO2, Pulse Rate Airflow, Snoring, CPAP Pressure Battery and Recording Time.
  • Compliant with the level IV of International sleep diagnosis standards
  • Evaluation of SDB and screening of OSAS
  • Determination of CPAP Pressure.
  • Online instant test score.

Technical Specifications

  • Oxygen Saturation Range : 0 to 100%
  • Pulse Rate Range : 30~240 BPM
  • Nasal/Oral Airflow Rate Range : 10~40/min

Wavelengths

Red : 60nm @ 3mw nominal
Infrared : 910nm @ 3mw nominal

Accuracy

SpO2 : 70 to 100% ± 3%
Pulse Rate : the larger ± of 3% and 1BMP

Resolution

SpO2 : 1%
Pulse Rate : 1BMP

Temperature

Operating : 5°C ~ 40°C
Infrared : -20°C ~ +55°C

Humidity

Operating : 15% to 95% non-condensing
Storage : 5% to 95% non-condensing

Atmosphere Pressure

Operating : 860 ~ 1060hPa
Storage : 500 ~ 1060hPa

Batteries Life

Operating : approx. 18 hrs ofcontinuous operation
Storage : 9 months typical

Power Requirement : 2 AAA Bateries

Dimensions : 62 x 57 x 21mm

Weight : 70g (without Batteries)

Type of Protection : Internally Powered (on battery power)

Degree of Protection : Type BF

Mode of Operation : Continuous