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controller CAVITY ASSESSMENT LED flashes red (Model 08-09 
RFCs) or a purging device message displays (Model 10 RFC) and an 
audible pulsed tone sounds throughout the purge procedure . When 
the tone and the LED/screen message stop, it is safe to insert the 
NovaSure disposable device .

CAUTION:

 CO

2

 continuously flows from the time that the disposable 

device is plugged into the controller until the CIA portion of the 
procedure is complete . To minimize the duration of CO

2

 flow 

and potential risk of embolism, perform the seating procedure 
immediately after inserting the disposable device and proceed 
directly from the seating procedure to the CIA .

WARNING:

 Use caution not to perforate the uterine wall when 

sounding, dilating or inserting the disposable device .

2 .16 Deploy the disposable device outside of the patient and ensure the 

controller ARRAY POSITION LED is extinguished (Model 08-09 RFCs) 
or the screen message does not display (Model 10 RFC) when the 
array is opened . If the LED is not extinguished (Model 08-09 RFCs) 
or the screen message is still displayed (Model 10 RFC), close 
and open the disposable device again . If this does not resolve the 
problem, replace the disposable device .

2 .17 Be certain the WIDTH dial reads greater than or equal to 4 .0 cm .

WIDTH dial

NOTE:

 If the WIDTH dial reads less than 4 .0 cm, close the disposable 

device and repeat step 2 .16 above . If the WIDTH dial still reads 
less than 4 .0 cm, open a new disposable device and return the old 
disposable device to Hologic Technical Support .

2 .18 Unlock the disposable device by pressing the lock release button . 

Close the disposable device by holding the front handle stationary 
and gently pulling the rear handle backwards until the closed array 
indicator, located at the hinge of the front and rear handles, reads, 
“ARRAY CLOSED” . This indicates that the array has been retracted 
into the sheath and the disposable device is in the closed position .

ARRAY 

CLOSED 

indicator

Lock release 

button

2 .19 Make sure the array is completely enclosed by the external sheath .
2 .20 Check that the WIDTH dial reads approximately 0 .5 cm .
2 .21 Using the uterine sound measurement and cervical canal 

measurements, consult the cavity length table (above) to obtain the 
appropriate cavity length settings as described in step 2 .10 above . 

CONTRAINDICATION:

 Do not treat a patient with a uterine cavity 

length that is less than 4 cm, as cervical canal damage may occur . 

2 .22 Using the cavity length table in section 2 .10, select the value 

obtained for length into the NovaSure RF controller input screen by 
depressing the UP/DOWN arrows . 

2 .23 Adjust and lock the cavity length setting feature on the disposable 

device to the value obtained above . (See step 2 .21 .) Ensure that the 
cervical collar is fully retracted to its proximal position .

2 .24 Confirm that the cervix is dilated to a minimum 6 mm (the nominal 

diameter of the NovaSure disposable device) . 

2 .25 Maintain a slight traction on the tenaculum to minimize the angle of 

the uterus .

2 .26 Angle the disposable device in-line with the axis of the uterus as 

the disposable device is inserted transcervically into the uterine 
cavity . By holding the front handle, advance the disposable device 
until the distal end of the sheath touches the fundus . 

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Содержание NovaSure Advanced

Страница 1: ......

Страница 2: ...d the disposable device may contain a more recent revision of the NovaSure system instructions than the manual provided with the controller The NovaSure disposable device is not to be used with other...

Страница 3: ...suctioning The disposable device is connected to the controller via a cord containing the RF cable suction tubing used for pressure monitoring during the cavity integrity assessment cycle and for suct...

Страница 4: ...hyperplasia a patient with any anatomic condition e g history of previous classical cesarean section or transmural myomectomy or pathologic condition e g long term medical therapy that could lead to...

Страница 5: ...the disposable device external to the patient to eliminate the risk of air or gas embolism The NovaSure RF controller CAVITY ASSESSMENT LED flashes red Model 08 09 RFCs or a purging device screen app...

Страница 6: ...after inserting the disposable device and proceed directly from the seating procedure to the CIA Electrically conductive objects e g monitoring electrodes from other devices that are in direct contact...

Страница 7: ...e g hormone D C or patient timing Patients randomized into the control arm received wire loop resection as an endometrial pretreatment Study endpoints The primary effectiveness measure was a validated...

Страница 8: ...rameters between the treatment groups between the age groupings or among the nine investigational sites Table 2 Patient Accountability Number of Patients NovaSure Wire Loop Resection Plus Rollerball E...

Страница 9: ...culty Performing Work Or Other Activities Due to Menses Pre operatively 66 3 65 5 Table 4 Effectiveness Quality of Life QOL NovaSure Wire Loop Resection Plus Rollerball 12 Months 9 9 8 6 24 Months 14...

Страница 10: ...use only in women who do not desire to bear children because the likelihood of pregnancy is significantly decreased following the procedure Patients of childbearing capacity should be cautioned of pot...

Страница 11: ...5 Press the toggle switch on the back panel of the controller into the on position 1 6 Connect the foot switch to the appropriate port on the front panel of the controller NOTE The first time the Mode...

Страница 12: ...ay can be extended CONTRAINDICATION Do not treat a patient with a uterine cavity length that is less than 4 cm as cervical canal damage may occur NOTE Patients with a uterine cavity length greater tha...

Страница 13: ...2 18 Unlock the disposable device by pressing the lock release button Close the disposable device by holding the front handle stationary and gently pulling the rear handle backwards until the closed...

Страница 14: ...eeze the disposable device handles together while gently moving the disposable device 0 5 cm to and from the fundus and rotating the handle of the disposable device 45 counterclockwise from the vertic...

Страница 15: ...m 2 34 Select the value indicated on the WIDTH dial into the NovaSure RF controller input screen by depressing the UP DOWN arrows 2 35 The system can be operated in either automatic mode or manual mod...

Страница 16: ...ting 24 Replacement Instructions 24 Specifications 24 Cleaning and Sanitizing 28 Parts List 28 Warranty 28 Technical Support and Product Return Information 28 Symbol Definitions 29 MODEL 08 09 RF CONT...

Страница 17: ...o be at the cervix and cannot be resolved by using the cervical collar use another tenaculum to grasp the cervix around the sheath Repeat the CIA by pressing the foot switch NOTE CO2 leakage may occur...

Страница 18: ...modification of this equipment is allowed Periodic maintenance Recommended periodic maintenance includes RF power output testing and standard safety tests such as leakage current in accordance with UL...

Страница 19: ...ated when the array is not fully deployed The ENABLE LED cannot be toggled on nor can power be delivered to the array when the ARRAY POSITION LED is illuminated VACUUM LED illuminates in two condition...

Страница 20: ...e new device abort the procedure NOTE Removing the disposable device from the uterine cavity after completing a cavity integrity assessment will require an additional CIA test to be performed upon dis...

Страница 21: ...2 leakage may occur at the external cervical os due to the presence of an over dilated cervix Visible bubbles or the hissing sound of escaping gas may accompany CO2 leakage under either of these condi...

Страница 22: ...ng and standard safety tests such as leakage current in accordance with UL 60601 1 along with regular cleanings described in the Cleaning and Sanitizing section RF power output test The NovaSure RF co...

Страница 23: ...r dilated cervix Visible bubbles or the hissing sound of escaping gas may accompany CO2 leakage under either of these conditions NOTE When following the troubleshooting steps on the Model 10 RFC press...

Страница 24: ...t still displays proceed with the following 2 Attempt gentle reseating of the NovaSure disposable device A Partially retract the array into the sheath by releasing the disposable device handle lock re...

Страница 25: ...ot appear Model 10 RFC Remove the NovaSure disposable device from the uterus after fully retracting the disposable device array into the sheath A Release the disposable device lock release button B Ho...

Страница 26: ...ent into an outlet on a circuit different from that to which the other device s is are connected Contact Hologic Technical Support or the manufacturer of the other equipment for assistance 5 The contr...

Страница 27: ...t s hand placed on her thigh should be avoided for example by insertion of dry gauze between skin surfaces WARNING With any electrosurgical device the potential for arcing exists and neuromuscular sti...

Страница 28: ...lectromagnetic site survey should be considered If the measured field strength in the location in which the RF generator is used exceeds the applicable RF compliance level above the RF generator shoul...

Страница 29: ...non Hologic Manufactured Equipment is warranted through its manufacturer and such manufacturer s warranties shall extend to Hologic s customers to the extent permitted by the manufacturer of such non...

Страница 30: ...Follow instructions for use Fragile Fuse High pressure HP Humidity limitation non condensing Keep dry Manufacturer No oil Not made with natural rubber latex Protect from heat Radio frequency RF energ...

Страница 31: ...MAN 03523 001 Rev 009...

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