Cegla RC-Test COPD Instructions Manual

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The Digital Pulmonary Function Test for COPD and Pulmonary Emphysema
COP D
TesT
PHYSIOLOGICAL BACKGROUND
The physiological background of the pulmonary parameters.
The one second capacity (FEV1)
measures in the first second the ma­ximum exhaled lung volume. This measurement predominantly mirrors a narrowing of the large airways. The six second capacity in contrast is the standard for the measurement of changes to the small airways. Unlike to the bronchi, the bronchio­le are not stabilized by cartilage, but rather, held open by elastic draws in the lung tissue. When inhaling deeply these draws cause the bronchiole to expand. When exhaling the draw of the lung tissue lets up due to the shrin­king lung volume which narrows the bronchiole even more.
The Six Second Capacity (FEV6)
measures the “rest” breathing volume after 6 seconds of exhaling. That is, at a point in time at which the retraction power of the lung volume, as descri­bed above, is significantly diminished. COPD is an illness which besides the larger airways (mucous buildup, nar­rowing) primarily effects the smallest airways and the pulmonary alveoli. This results in dissolution of the setting of the smallest airways and thereby causing a diminished holding open of these bronchial parts during exhaling. The FEV6 mirrors therefore the distur­bances in the pulmonary periphery si­gnificantly better than the FEV1. From the ratio FEV1/FEV6 the narrowing of the smallest airways can be determi­ned. With illnesses such as pulmonary fi­brosis (an airway restricting illness) the fibrosis affected lung tissue of the bronchiole is pulled apart, so that with a generally diminished FEV1 (due to diminished lung volume with pulmona-
ry fibrosis) the FEV6 is in comparison significantly increased. With COPD we observe disturbances, which can be (partially) rectified with medicine and other changes which are caused by physical disturbances of the lung tissue and thereby cannot respond to medicine. Here the physical therapy, for example with the RC-Cornet (basic cornet), can help. This respiratory therapy device loosens mucous, stabilizes and expands the small bronchi and reduces shortness of breath of the patient.
Detailed instructions for use are availa­ble at www.cegla.de.
07/2015
Article-no. 160EN PPN 1107 1177 1670
The related products as well as accessories for the RC-Test are available in pharmacies, medical supply stores or at www.cegla-shop.com.
RC-Cornet
®
Respiratory Therapy Device Loosens mucous, reduces short­ness of breath and coughing. Article-no. 210EN PPN 1108 4186 6756 PIP 392-5542
Oxygen cannula craton adults
Comfortable to wear due to the soft kraton nose tips. Article-no. 710EN PPN 1103 3673 0429
Oxygen cannula phthalate-free adults
With soft kraton nose tips, free of phthalate (plasticizers). Article-no. 760EN PPN 1110 3980 1541
RELATED PRODUCTS
INSTRUCTIONS FOR USE
0
1
2
3
Normal
I
II
III
IV
Obstruction
Index
COPD-
Classifi-
cation
FEV1/ FEV6-
ratio and
FEV1 value in % of
the standard value (SV)
FEV1 /FEV6 0,70
FEV1 /FEV6 < 0,70 &
FEV1
80 % of the NW
FEV1 /FEV6 < 0,70 &
FEV1 < 80 % of the NW
FEV1 /FEV6 < 0,70 &
FEV1 < 50 % of the NW
FEV1 /FEV6 < 0,70 &
FEV1 < 30 % of the NW
FEV1-Value
iin % of
the standard
value
80 %
< 80 %
< 50 %
< 30 %
DISPLAY EXPLAINATION
Please read the instructions for use of the RC-Test COPD carefully before first use.
Manufacturer: R. Cegla GmbH & Co. KG Horresser Berg 1 56410 Montabaur Germany
www.cegla.d e
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RC-TEST PREPARATION APPLICATION DESCRIPTION
Normal
Notice that both arrows point to the green area!
Possible COPD or Emphysema Result
A possible COPD indica­tion results when the left arrow points to the yellow
area and the right arrow indicates a number I to IV. Recommendation: Spirometer Examination
Possible Restriction Result
Indications of a restrictive
pulmonary illness, for
example fibrosis, result
when the left arrow points to the yellow area and the right arrow to the green area. COPD indication is unlikely. Recommendation: Spirometer Examination
Indication of severe COPD
When the left arrow
points to the red and
the right arrow indicates
a number III to IV, then
that is a sure indication
of severe COPD. Recommendation: Spirometer examinationCOPD.
Display of the pulmonary function parameters
1. The display shows
the FEV1 (absolute) and the FEV1 in % of the
standard value. Each value of the breathing maneuver is dis­played until the enter key is pushed.
2. By pushing the
-key you can check
the following displays one after the other:
a) a. FEV6 (absolute)
and FEV6 in % of the
standard value
b) a. FEV1/FEV6 ratio
and FEV1/FEV6 in %
of the standard value
c) a. Estimated
biological age of the
lung
TEST ASSESSMENT CLEANING AND DISINFECTION
Battery charge condition
Now blow
Bad maneuver (delayed start or cough)
Biological lung age
Age
Size
Sex
DEVICE SYMBOLS
Device Head
Device Body
Before first use, please put in the bat­teries.
1. Fasten the mouth piece* onto the device.
3. After the battery indicator goes out then the device is ready for use.
4. Enter the age of the patient and confirm the entry with the enter key.
5. Enter the size of the patient and confirm the entry with the enter key.
6. Enter the sex of the patient and confirm the entry with the enter key.
All surfaces should be cleaned weekly (wiped down), more often when nee­ded. We recommend for cleaning the use of disinfectant disposable wipes. Special attention should be paid to the device head. To clean or disinfect please remove the device head with a light tug from the device body. Now the device head can be soaked in a soap water bath or disinfectant solution for 15 minutes. Afterwards rinse with warm water to accelerate the drying process. The device body itself may not come into contact with water.
* With the RC-Test COPD can be used the safety
mouthpiece (per patient | no to be cleaned | article-no. 460EN or the reusable mouthpiece (for one patient | article-no. 180EN). Mouthpie­ces are available separately in pharmacies or at
www.cegla-shop.com
The patient must position the device in the hand so that the backside opening is not covered. The patient stands upright, inhales deeply and encloses the mouth­piece tightly with his/her lips. Afterwards he/she exhales as fast and as powerful as possible for 6 seconds.
After 6 seconds a beep will sound. Afterwards the exhaling maneuver should be carried out another two times.
The device recognizes a bad or an insufficient exhale maneuver and shows this as a ! on the display.
The best test can be displayed with the enter key.
If the device is not used for two minutes then it automatically turns itself off.
To turn the device off please hold down the power button for three seconds.
2. Turn on the device.
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