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Welcome to Niche Medical's Customer Newsletter. If you missed our
first newsletter you will find a copy in the News section on our
website at www.nichemedical.com.au
This newsletter is designed to inform our customers of the latest
information on our products and services. We aim to include
information on best practice, continuing education, equipment
operation and clinical updates. In every issue, we will also feature
one institution or individual using our products and we would value
your input and feedback. Please send all articles and feedback to
Craig Abud - craig@nichemedical.com.au
Our goal is to provide you with valuable information in a format
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| Vapotherm® Competition Winner - TSANZ / ANZSRS
Conference Perth, March 2005 |
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Congratulations to Jenny Busch of the Royal Hobart Hospital
on winning an Apple i-Pod® in our Vapotherm® Competition at
the recent TSANZ / ANZSRS Conference in Perth. Thank you to
all delegates who entered our competition.
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| Vapotherm® High Flow Gas Therapy via Nasal Cannula for
Respiratory Insufficiency |
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Study Title: High Flow Gas Therapy via Nasal Cannula
for Respiratory Insufficiency.
Study Authors: Joy Sarkisian-Donovan RRT; John J
Hill, RRT Respiratory Care Staff; Michael J Neary MD; David
M.F. Murphy MD.
Study Site: Deborah Heart and Lung Center, Brown
Mills, NJ, USA.
Publication: RESPIRATORY CARE Journal, November
2004, Volume 49, No. 11.
Introduction: High flow gas therapy (HFT) via nasal
cannula (NC) is a recent development for the treatment of
patients with respiratory compromise. HFT delivers high flows
of up to 40 litres per minute (lpm) supplemental gas at BTPS
(Body Temperature Pressure Saturated) which patients find
comfortable. In this study, we used HFT in lieu of
non-invasive or invasive ventilation for patients with
respiratory insufficiency. Respiratory insufficiency was
defined as an increasing demand for supplemental oxygen along
with decreasing oxygen saturation (Sa02%) and increasing
respiratory rate (RR).
Method: Subjects with respiratory insufficiency were
sequentially placed on HFT. All HFT measurements were
recorded. A subjective modified Borg scale for dyspnea
assessment was recorded after placement on HFT. HFT was
delivered using the Vapotherm® 2000i system. Failures on HFT
were advanced to non-invasive or invasive ventilation. HFT was
delivered via NC with temperature and flow rates titrated to
patient comfort and oxygenation requirement. Recorded
measurements post placement of HFT at time intervals of 30-60
minutes included RR and Sa02% measured by pulse oximetry.
Results: Twenty-nine patients (29) were studied
There were 10 females and 19 males. The mean age was 65 years
(range of 16-84 years). Prior to initiation of HFT the mean
respiratory rate was 25 bpm (range of 14 to 40 bpm), the mean
Sa02% was 88% (range 78% - 95%). Supplemental oxygen in the
control group was delivered using standard techniques
including Nasal Cannula at 6 lpm (six patients) and Venturi or
Non-Rebreather Mask (twenty-three patients).
After administering HFT the mean respiratory rate was 20
bpm (range of 14 - 29), mean Sa02% was 97% (range 90% - 100%),
the mean Fi02 requirement was 86% (range 35% - 100%) titrated
using an oxygen blender, with a mean flow rate of 28 lpm
(range 20 - 40 lpm). The mean temperature was 37 degrees
celsius (28 patients at 37 degrees celsius, 1 patients at 36
degrees celsius). Using a one-tailed, paired, t-test, there
was a significant decrease in the respiratory rate (RR) for
HFT compared to the Pre-HFT (p=0.0001). There was a
significant increase in Sa02% with HFT compared to Pre-HFT
(p=0.000004). No patient using HFT required subsequent
non-invasive or invasive ventilation.
Conclusion: Vapotherm® HFT significantly increased
Sa02% and significantly decreased RR in all 29 patients in
this study. HFT can improve acute respiratory insufficiency in
patients without discomfort as indicated by patient response
to the Borg scale questionnaire. HFT at flows up to 40 lpm via
Nasal Cannula may be considered as an alternative to more
agressive respiratory therapy such as non-invasive or invasive
ventilation.
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| The Effects of Vapotherm® High-Flow vs. Low-Flow Oxygen
on Exercise in Advanced Obstructive Airways
Disease |
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Study Title: The Effects of High-Flow vs Low-Flow
Oxygen on Exercise in Advanced Obstructive Airways Disease.
Study Authors: Wissam Chatila, MD; Tom Nugent, MD;
Gwendolyn Vance, RN; John Gaughan, PhD; and Gerard J. Criner,
MD.
Study Centre: Division of Pulmonary and Critical
Care Medicine, Department of Medicine; Temple University
School of Medicine, Philadelphia, P.A, USA.
Study Objectives: Current options to enhance
exercise performance in patients with COPD are limited. This
study compared the effects of high flows of humidified oxygen
to conventional low-flow oxygen (LFO) delivery at rest and
during exercise in patients with COPD.
Study Design: Prospective, nonrandomized, nonblinded
study.
Study Setting: Outpatient exercise laboratory.
Patients: Ten patients with COPD, stable with no
exacerbation, and advanced airflow obstruction (age, 54 +/- 6
years; FEV1, 23 +/- 6% predicted [mean +/- SD]).
Interventions: After a period of rest and baseline
recordings, patients were asked to exercise on a cycle
ergometer for up to 12 minutes. Exercising was started on LFO
first; after another period of rest, the patients repeated
exercising using the high- flow oxygen (HFO) system, set a 20
L/min and matched to deliver the same fraction of inspired
oxygen (FI02) as that of LFO delivery.
Measurements and results: Work of breathing and
ventilatory parameters (tidal volume, respiratory rate,
inspiratory time fraction, rapid shallow breathing index,
pressure-time product) were measured and obtained from a
pulmonary mechanics monitor. Borg dyspnea scores, pulse
oximetry, blood gases, vital signs were also recorded and
compared between the two delivery modes.
Patients were able to exercise longer on high flows (10.0
+/- 2.4 min vs 8.2 +/- 4.3 min) with less dyspnea, better
breathing pattern, and lower arterial pressure compared to LFO
delivery. In addition, oxygenation was higher while receiving
HFO at rest and exercise despite the matching of FI02.
Conclusion: High flows of humidified oxygen improved
exercise performance in patients with COPD and severe oxygen
dependency, in part by enhancing oxygenation.
Please click on the below link to view the entire
publication - this link requires a subscription to CHEST
online.
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Evaluation of the EasyOne® Spirometer for Paediatric
Use: A Pilot Study |
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Study Author:
- Andrew D. Coates, Lung Function Laboratory, Mater
Misericordiae Health Services, Brisbane.
Background:
- Spirometers for paediatric use must be well constructed,
be accurate at both high and low volumes and flows and be
easy to hold in a child's hands. Mouthpiece size, child
incentive software, stringent infection control needs, and
ease of use of software are also important.
- Most spirometers are marketed directly for adult patient
use. The current ATS Standardization of Spirometry is
largely focused on adult testing, and spirometers are
usually marketed with agreement to those recommendations.
[1]
- The ndd Medical Technologies EasyOne® spirometer has
features suitable for testing children.
Aim:
- To investigate the accuracy of the EasyOne® spirometer
for use in a paediatric service.
Method:
- Compare spirometry measures in a group of children
tested using the EasyOne® and a Laboratory- based
SensorMedics Vmax 20c® spirometer.
- The EasyOne® was used in PC-mode without the child
incentive display.
- The EasyOne® does not require re-calibration.
Calibration checks were made prior to each session using a
3-Litre Calibration Syringe. The Vmax® was calibrated
prior to each session using the same syringe.
- Children attending clinics were initially tested on
the Vmax® and then on the EasyOne® spirometer.
- Following the BTS/ARTP Spirometry guidelines, the
children stood and wore noseclips. [2]
- Agreement assessed using SPSS software with Student's
paired-T tests and Bland Altman plots.
Results:
- 12 children agreed to be studied. [4M: 8F, ages 5- 15,
10.4 mean (3.6 (SD)]
- Spirometry on both systems was determined to be
acceptable and reproducible. [2]
- Child ilnesses were asthma (2), post-Chronic Neonatal
Lung Disease (2), Cystic Fibrosis (7), and pre-scoliosis
correction (1).
- Only the FVC parameter showed a statistically
significant bias of 95ml in favour of the EasyOne®.
Discussion:
- FVC Bias of 95ml (EasyOne®) unlikely to be clinically
significant. Repeatability of 100ml is sought in children.
[2]
- The small samples size may be why statistical
significance was not seen for the other biases.
- The EasyOne® spirometer appears to have the required
accuracy for use in paediatrics.
- Given the EasyOne's® accuracy, proceed to design a
full evaluation trial for paediatrics. This should be a
multiple arm study - e.g. 30 asthmatics, 30 CF, 30
controls.
- Further investigation of the acceptability of the
EasyOne® should include studying the two modes of use
(portable and PC-based), the child incentive software, and
the utility of the quality grading system.
Conclusions:
- In paediatrics, EasyOne® spirometry measures compare
well with the Vmax® Laboratory-based spirometer.
- Further full evaluation warranted.
Acknowledgements:
- This poster was presented at the recent ANZSRS
(Australian and New Zealand Society of Respiratory
Science) Conference in Perth, where it was awarded as Best
Poster. I gratefully acknowledge the ANZSRS for the
opportunity of presenting my work. My thanks also to
Gordon Williams for designing this poster.
References:
- Standardization of Spirometry, 1994 Update. American
Thoracic Society. Am J Respir Crit Care Med, 1995. 152(3):
p. 1107-36.
- Guidelines for the measurement of respiratory
function. Recommendations of the British Thoracic Society
and the Association of Respiratory Technicians and
Physiologists. Respir Med, 1994. 88 (3): p. 165-94.
View the full poster in pdf
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