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Cleaning and Infection Control of the Digitest II

•   DO NOT AUTOCLAVE THE DIGITEST II POWER 

UNIT, AS THIS WILL CAUSE DAMAGE TO IT.

•  Ideally, the Power Unit should be protected using 

appropriately-sized disposable plastic barrier 

sleeves. Since the Digitest II incorporates sophis-

ticated electronic circuitry, it should not be directly 

sprayed with or soaked in disinfectant. The device 

may be disinfected by wiping it with a damp cloth or 

paper towel sprayed with an EPA-approved high-

level surface disinfectant, and dried with a paper 

towel. Follow the surface disinfecting protocol 

specified by the disinfectant manufacturer.

•   Autoclaving does not remove accumulated  

debris. Before autoclaving, scrub the autoclavable 

components with a brush, or clean in an ultrasonic 

cleaner, using warm, soapy water.

•  The Tooth Probes, Lip Clip and Wire Assembly may 

be sterilized in any conventional steam autoclave 

(132-135C for 15 min for gravity displacement or  

4 minutes for prevacuum cycle, or using the manu-

facturer’s recommended procedure, if different). 

Minimum cool down interval is 15 min.

Service and Maintenance

•   Do not open the Power Unit, except to change the 

battery. There are no user-serviceable parts inside. 

Internal repairs are to be made only by authorized 

Parkell personnel, by returning the unit to the  

service address at the end of these instructions.

•  Avoid dropping the Power Unit or subjecting it to 

physical shock.

•  Battery should be removed if unit is to be stored 

unused for more than 30 days.

•  To prolong battery life, the device automatically 

turns off after 14 seconds of inactivity.

•  When the battery capacity is low, the Left and  

Right digital display digits will flash alternatively 

while the unit is activated. Replace the battery as 

explained in the section “Changing the Battery”.

•  If a Tooth Probe becomes loose in the mount of  

the Power Unit, it may be tightened by carefully 

inserting a flat screwdriver blade into the split  

metal base of the probe and gently expanding  

the sides apart with a twist of the tool.

•  Discard and replace any Tooth Probe if the  

metal or the insulation becomes damaged  

during use. 

Changing the Battery (Figure 2) 

•  The Digitest II Pulp Vitality Tester comes with a 

high-output, 9 Volt alkaline battery factory installed.

•  The replacement battery may be a Radio Shack 

23-553, Duracell MN1604, Panasonic 6AM6  

or equivalent. Although rechargeable 9 Volt  

batteries may be utilized, they will require more 

frequent changing and charging because of the 

considerable voltage required to perform the pulp 

testing procedure.

•  To replace a weak battery, remove screw (A) and 

carefully lift off the plastic battery door (B) by gently 

pulling it away from the Power Unit. Withdraw the 

weak battery from the battery enclosure, and  

unsnap the wire battery connector. Discard  

battery in accordance with all applicable  

environmental laws.

•  The fresh battery should be snapped onto the  

connector and placed in the Power Unit so the 

top end attached to the connector is placed first 

into the opening. Slight pressure on the bottom of 

the battery will help it to slide home. Replace the 

plastic battery door (B) by engaging the tabs on the 

bottom first, and tighten the screw (A) gently.

Digitest II Setup, Prior to Performing  

Pulp Vitality Testing

•  Standard infection control 

protocol should be followed 

during pulp testing, by wearing 

disposable rubber, vinyl or 

nitrile gloves. When wearing 

gloves, the circuit 

is completed by 

using the autoclav-

able Lip Clip and 

Wire Assembly. 

Plug one end of the 

wire assembly onto 

the socket on the 

bottom of the Power Unit (C), and insert the Lip Clip 

(D) into the other socket. Place a small amount of 

toothpaste on the lip to enhance electrical conduc-

tivity, and then place the Lip Clip over the patient’s 

toothpaste-coated lip, making good contact with 

the mucosa.

•  Although it is strongly recommended that gloves be 

worn when performing vitality testing to maintain 

accepted standards of infection control, if gloves 

are not being worn, the ground wire need not be 

used. The operator may complete the circuit by 

making contact with the metal plate of the unit  

and touching the patient’s cheek or chin with the 

free hand.

•  Remember that to accurately diagnose the condi-

tion of the tooth, pulp testing must be performed  

on a patient who has not been anesthetized or  

received gas analgesia. Make sure to use the 

Digitest II tester BEFORE you administer local 

anaesthesia or gas analgesia.

 •  The tooth to be tested and the adjacent teeth must 

be clean and dry. Interproximal embrasures should 

be made free of any impacted food debris, saliva, 

water or plaque by flossing or scaling with an 

instrument and air-drying before testing.

•  It is often useful to electrically isolate the tooth 

being tested from neighboring teeth or metallic 

restorations by wrapping it with a clear mylar  

strip, such as those used in fabricating Class III 

composite restorations.

•  A dry cotton roll should be placed in the  

buccal vestibule to isolate the tooth from the lip 

and cheek.

•  A plastic mirror should be used to keep the tongue 

off of the tooth during testing.

•   Insert Tooth Probe (E) into 

the open end of the Power 

Unit. To enhance electrical 

conductivity and contact 

between tooth and probe, 

apply a small amount of 

toothpaste to the metal tip.

•   Metal or ceramic surfaces cannot be used as 

touch points for the Tooth Probes. Teeth selected 

for pulp testing must possess enough exposed 

enamel or dentin to allow the probe to make 

contact without touching the gingiva or a metal 

restoration. In certain cases, this may require the 

use of a Precision Probe (included).

•   Fully instruct the patient as to what you will be  

doing, so they are not surprised during the test.

•   Tell the patient that when the vitality test is  

underway, they should carefully raise their hand  

at the first sign of sensing the stimulus. This 

should avoid any patient discomfort. 

Pulp Vitality Testing with the  

Digitest II Pulp Vitality Tester

1)  To activate the unit, press 

and hold the start button (F) for 

a half second, and then release 

the button. When the button is 

depressed, the display will show 

one row of horizontal bars if the 

device is set for “SLOW”, two 

rows for “MEDIUM”, or three rows for “FAST”. When 

the button is released, the display will read “00”, 

indicating that it is ready to begin the vitality test. 

The display will shut off if the unit is not used within 

14 seconds.

2)  If the desired stimulus rate 

mode was displayed, the vitality 

test may proceed, as detailed in 

Step 4.
3)  If you wish to change the  

stimulus rate mode, repeatedly press and release 

the button twice in quick succession. The display 

will cycle between the three stimulus rate modes. 

When the desired setting is displayed, press the 

button one more time to let the display return to 

“00”, so the test may begin.

NOTE: The unit will remember the last  

stimulus rate mode setting, even if the device  

is powered down.

4)  Place the toothpaste-covered tip of the Tooth 

Probe on the middle of the labial or lingual surface 

of the tooth. Avoid soft tissue and restorations such 

as crowns, amalgams or composites.
5)  Depress and hold the button, and the display 

number will rise, indicating that a gentle-pulse 

stimulus is being automatically applied to the tooth. 

When the patient indicates that they feel the stimu-

lus, release the button. The stimulus will stop im-

mediately. The display will freeze and hold the final 

reading for approximately 14 seconds, so it may be 

noted. The unit will then automatically turn itself off.
6)  The maximum stimulus reading is 64. Even if 

there is no response at this level, there is still the 

possibility that the tooth is vital. No sensation at 

this number simply suggests that the tooth is non-

responsive at the time of the test. However, since 

teeth have been known to recover from traumatic 

injury many days after presenting with a “non-vital” 

reading, follow up testing is almost always indicated 

after any initial readings. If this reading persists over 

several visits, it is reasonable to assume that the 

tooth is non-vital. However, this conclusion should 

always be confirmed by another accepted endodon-

tic testing method.
7)  To verify the reading, a corresponding control 

tooth in the same arch should be tested. Molars 

should be matched to molars, premolars to premo-

lars, cuspids to cuspids, and incisors to incisors. 

If this is not possible because teeth are absent, 

endodontically treated, or have full coverage resto-

rations, a similar tooth in the opposite arch should 

be used.

Clinical Observations

•   It is not possible to prepare a “table of normal 

values” for pulp tester readings, because THERE 

IS NO “NORMAL” IN PULP TESTING. Rather, the 

clinician should perform sequential comparisons 

between the subject tooth and the control tooth 

at consecutive office visits, observing how the 

readings are changing as time progresses. By 

utilizing electric pulp testing, along with all avail-

able diagnostic information, it is often possible to 

predict where the tooth’s vitality is heading. This 

allows the clinician to make informed decisions as 

to whether endodontic therapy is appropriate, and 

whether it is prudent to simply watch and wait.

•  There are general anatomic trends in pulp vitality 

readings. Posterior teeth generally require greater 

stimulus than anteriors, probably because of the 

greater thickness of enamel and dentin in posterior 

teeth. Enamel requires a greater stimulus than 

dentin or cementum, because of the higher per-

centage of non-conductive mineral, and the lower 

percentage of water. Cross-arch teeth, or oppos-

ing teeth will have similar thresholds to stimulus.

•  The stimulus threshold may also be affected by 

such factors as the age, gender and previous pain 

history of the patient, pulp chamber size, trauma, 

pathology and use of prescription and non-pre-

scription medications, or illicit drug use. 

A

D

E

SLOW

MEDIUM

FAST

READY

B

Fig. 2

F

C

Continued

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