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Abstract
Introduction: A final flush with chelating agents and other test groups in the apical third. Conclusion: Root canal cleanliness benefits
antiseptic irrigating solutions is needed to remove the from solutions activation (especially sonic activation and manual-dynamic activation)
smear layer. The improvement of these protocols is in comparison with no activation during the final irrigation regimen. (J Endod
possible by using specific delivery and agitation tech- 2010;-:1–6)
niques. This study examined the effect of different final
irrigation regimens and methods of activation on smear Key Words
layer removal in curved canals after root canal instru- Automated-dynamic activation, final irrigation, manual-dynamic activation, smear
mentation. Methodology: Mesial root canals of 50 ex- layer, sonic activation
tracted mandibular molars were prepared using
ProTaper rotary files (Dentsply Maillefer, Ballaigues,
Switzerland) and 3% NaOCl. Teeth were then allocated
to two control groups and four experimental groups (n
T he ultimate goal of endodontic treatment is to control the microbial factor in
complex root canal anatomy, especially in the apical one third (1). This objective
is achieved by combining instrument-based preparation (manual or mechanical)
= 10) for final irrigation as follows: no-activation group with antiseptic irrigating solutions followed by three-dimensional obturation of the
(final rinse with a 27-gauge needle and 17% EDTA/3% root canal system. The gold standard irrigant is still sodium hypochlorite, which can
NaOCl), manual-dynamic activation group (final rinse be associated with EDTA to offer bactericidal, solvent, and chelating actions all in
17% EDTA/3% NaOCl + gutta-percha agitation), one. This combination offsets the drawbacks of the instrument-based preparation,
automated-dynamic activation group (final rinse 17% particularly the creation of debris (2) and the smear layer (3). The smear layer is poten-
EDTA/3% NaOCl + RinsEndo [Dürr Dental GmbH & Co tially infected, and its removal allows more efficient penetration of intracanal medica-
KG, Bietigheim-Bissingen, Germany]), and sonic- tions into the dentinal tubules and a better interface between the filling material and the
activation group (final rinse 17% EDTA/3% NaOCl + En- root canal walls (4).
doactivator [Advanced Endodontics, Santa Barbara, The literature reports generally show that regardless of the instrumentation and
CA]). All mesial roots were split with a new approach irrigation techniques, the effectiveness of irrigating solutions remains limited in the
to allow visualization of every third of the canal, partic- apical one third of a prepared canal. This is particularly true for curved root canals
ularly the apical third. The samples were prepared for (5, 6) and even on single-rooted teeth (7, 8). Therefore, the improvement of
scanning electron microscopic observation to assess irrigating protocols is essential during root canal treatment in order to achieve
the smear layer removal. Blind scoring was performed better cleaning efficiency especially in the very complex apical area.
by two calibrated observers using a five-score scale. Currently, several techniques and systems are available and reported to improve
The differences in smear layer scores between the exper- final irrigation before obturation (9). Among these protocols passive ultrasonic irriga-
imental groups were analyzed with the Kruskal-Wallis tion has shown promising results on debris (10) and smear layer removal (11).
test and the Mann-Whitney U test. The level of signifi- However, there are little published scientific data comparing the new and
cance was set at p = 0.05. Results: Very high levels emerging devices and methods for disinfection with a conventional syringe irrigation.
of root canal cleanliness (#score 3) were found for First, a fully tapered and apically trimmed nonstandardized gutta-percha master cone
each test group with activation. For the middle and could be used in a well-prepared canal as a cost-effective mechanical agitator. A gentle
apical third, the no-activation group was significantly pumping with short vertical strokes has been shown to promote disinfection (12, 13).
less effective than the three other activation groups (p Another recently released device, the RinsEndo irrigation system (Dürr Dental GmbH &
< 0.05). The manual-dynamic activation group (final Co KG, Bietigheim-Bissingen, Germany), delivers solutions at a flush-through rate of 6.2
rinse 17%EDTA/3%NaOCl + gutta-percha agitation) mL/min using pressure-suction technology for intracanal activation (1.6 Hz). This
and the sonic-activation group (final rinse 17%EDTA/ device generates a mechanical action that is able to produce a hydrodynamic exchange
3%NaOCl + Endoactivator) showed significantly better circuit (13, 14). Finally, the Endoactivator system (Advanced Endodontics, Santa
smear layer removal (p < 0.05) in comparison with the Barbara, CA) has been purported to improve disinfection. This device uses
From the )Department of Endodontics and Restorative Dentistry, School of Dentistry, University, Paris, France; and †Department of Surface Physico-Chemistry,
ENSCP, Paris, France.
Supported in part by the Association de formation en Endodontie Appliquée.
Address requests for reprints to Dr Gregory Caron, 5 rue Garanciere 75006 Paris , France. E-mail address: greg.hypomoclion@gmail.com.
0099-2399/$0 - see front matter
Copyright ª 2010 American Association of Endodontists.
doi:10.1016/j.joen.2010.03.037
JOE — Volume -, Number -, - 2010 Final Irrigant Activation Protocols for Smear Layer Removal in Curved Canals 1
ARTICLE IN PRESS
Basic Research—Technology
a cordless sonic handpiece to activate strong, highly flexible polymer The frequency of activation used was 100 push-pull strokes per minute
tips. Noncutting tips have tapers and terminal diameters that closely (12). The canals were then flushed with 3 mL of a 3% solution of
match the dimensions of the final root canal preparation (15). Mechan- sodium hypochlorite. This solution was then activated for 30 seconds
ical oscillations are produced mainly at the tip of the activator with per canal using the pumping master cone method.
a frequency ranging from 1 to 10 kHz. Automated-dynamic Activation Group. After optimally
The purpose of this study was to assess smear layer removal effi- preparing the canal, surplus NaOCl was suctioned away with the
ciency after using gutta-percha master cone or RinsEndo or the Endoac- 27-gauge needle. Following the manufacturer’s instructions, each canal
tivator in comparison to conventional final irrigation using a 27-gauge was flushed with 1 mL of 17% EDTA using the RinsEndo system for 1
needle. The null hypothesis was that there is no difference in smear layer minute per canal. Each canal was then flushed with 3 mL of a 3% solu-
removal between final irrigation with no activation and final irrigation tion of sodium hypochlorite delivered via the RinsEndo system for 30
with activation. seconds in each canal.
Sonic-activation Group. After optimally preparing the canal,
Materials and Methods surplus NaOCl was suctioned away with the 27-gauge needle. Each canal
The study was conducted on 50 freshly extracted mature human was then irrigated with 1 mL of 17% EDTA using the 27-gauge needle.
mandibular molar teeth with two separate mesial canals. None of the This intracanal solution was activated with either a red (25/04) or blue
teeth had received restorative or endodontic treatment before extrac- (35/04) EndoActivator tip at a speed of 10 kHz for 1 minute per canal.
tion. After extraction, the teeth were conserved in a solution of physio- Each canal was then flushed with 3 mL of 3% sodium hypochlorite. This
logic saline to avoid damaging the pulp tissue and then stored at 4 C solution was then activated using either the red or blue EndoActivator tip
(16). Each individual tooth was then photographed and x-rayed to visu- for 30 seconds per canal.
alize the root canal anatomy and confirm that each canal curved at more After activation, the action of the sodium hypochlorite was stopped
than 20 (17). by syringing in 3 mL of physiologic saline solution per canal (ie, 6 mL for
After cutting a four-wall access cavity, the full lengths of the mesio- each tooth in the four test groups). All the samples were then placed in
buccal and mesiolingual canals were determined when a #08 K-type file a solution of physiologic saline and stored at 4 C until proceeding with
could be visualized at the apical foramen. Both the mesial and distal the sectioning protocol.
roots were sealed with melted wax to close the apical foramen (18).
The aim was to prevent the irrigants from escaping through the apex Sectioning of the Teeth and Preparation for SEM
in order to simulate in vivo conditions (19). The two mesial root canals The teeth were sectioned in two halves; only the mesial root was
were prepared using the Protaper Universal rotary files system (Dents- kept for further study. Two horizontal grooves were made using a Frios
ply Maillefer, Ballaigues, Switzerland) following the protocol described diamond-cutting disk (Microsaw; Dentsply Friadent, Mannheim,
by Machtou and Ruddle (20) in which the apical one-third taper of the Germany) mounted on a surgical dental handpiece to separate the
finished preparation is approximately 10%. All the canals were mesial root into thirds (the apical third, the middle third, and the
prepared so that the finished size of each apical foramen ranged coronal third). This step was performed using a surgical microscope.
between 0.20 mm and 0.30 mm in diameter. A medium nonstandar- Colored gutta-percha cones were fitted and used as markers to best
dized gutta-percha master cone (Henry Schein, Melville, NY) was fitted gauge groove depth. The objective was to avoid any intrusion of the
in each canal to the full working length, and then the tooth was x-rayed. cutting disc into the canals, which would pollute the samples by splat-
After each instrument, the expending preparation was flooded by tering cutting debris into the root canal system. To avoid any contami-
passively irrigating 0.5 mL of 3% sodium hypochlorite (Parcan; Septo- nation, coronal thirds were discarded because there was a bigger gap
dont, Saint-Maur-des-Fosses, France) into the canal using a 27-gauge between the gutta-percha markers and the prepared walls of the canal.
needle (Monoject; Tyco Kendall, Hampshire, UK) loosely inserted as This gap compromised vision and increased the possibility of the cutting
far as possible without binding. A #10 K-type patency file was used to disc inadvertently introducing debris into this region of the canal.
maintain apical patency and move debris into suspension followed by The apical and middle one thirds of the canal were then
flushing the canal again with 0.5 mL of fresh irrigant. All procedures sectioned in the longitudinal plane with a precision diamond bur
were performed by the same operator (GC). (889 Model; Komet, Paris, France). A continuous supply of air was
The teeth were randomly divided into four experimental groups (n delivered to improve vision and cutting precision, which eliminated
= 10) and two control groups. The negative controls (n = 5) received the potential of introducing debris into this region of the canal.
no final irrigation regimen after fitting of the master cone. The positive Each third was vertically split by applying slight pressure to an enamel
controls (n = 5) were immersed for 5 minutes in a bath of 17% EDTA chisel into the longitudinal groove. Each sample was dehydrated in
followed by an immersion for 5 minutes in a bath of 3% NaOCl after the graded series of ethanol solutions, critical point dried, coated with
splitting process. gold, and viewed with a scanning electron microscope (Hitachi
S2500,Verrieres-le-buisson, France) at 15 kV (Fig. 1).
Final Irrigation Protocols
No-activation Group. After suctioning away the intracanal surplus SEM Evaluation and Statistical Analysis
of NaOCl with the 27-gauge needle, 1 mL of 17% EDTA (Largal Ultra; Each fragment was first viewed at low magnification (30) by the
Septodont, Saint-Maur-des-Fossés, France) was flushed into each canal operator (GC) and another trained dentist with SEM studies (KN) in
and was left in place for 1 minute per canal. All canals were then flushed order to gain an overview of the sample. Image acquisition on the
with 3 mL of 3% sodium hypochlorite, which was left in place for 30 most typical zones of the sample was performed at a magnification of
seconds per canal. 1,000 to assess the presence of smear layer. The images were blindly
Manual-dynamic Activation Group. After suctioning away the assessed by two practitioners with no inside knowledge of the operative
intracanal surplus of NaOCl with the 27-gauge needle, 1 mL of 17% procedures and who were fully conversant with qualitative analysis on
EDTA was flushed into each canal. This solution was activated by using root canal images produced by scanning electron microscopy (PM,
a gutta-percha cone as previously described for 1 minute in each canal. FB). Analysis began using the scale described in Hülsmann et al
Figure 1. Four different apical sample fragments highlighting the reproducibility and preservation of the apical one-third samples using our experimental protocol.
Magnification: 30.
(21), but the significant lack of sensitivity in the best scores prompted at a = 0.05. All statistical analyses were performed with the SPSS for
us to refine the system, as follows (Fig. 2): score 1: no smear layer and Windows 12.0 software package (SPSS Inc, Chicago, IL).
dentinal tubules open, score 2: small amounts of scattered smear layers
and dentinal tubules open, score 3: thin smear layer and dentinal
tubules partially open (characteristic image of crescent), score 4: Results
partial covering with a thick smear layer, and score 5: total covering After consensus was reached for each group, mean scores for
with a thick smear layer. smear layer removal in the apical third and the middle third were listed
First, the full set of samples was independently evaluated by two (Table 1). The full set of negative control samples scored a 5 with
observers (PM and FB). If there were conflicting results between these a complete covering of a thick smear layer. All the positive control
two observers, then a final evaluation was made with the lower score samples scored a 1 with no visible smear layer. In the middle third,
chosen every time. Nonparametric data were analyzed by using the comparisons between each group showed a statistically significant
Kruskal-Wallis test and the Mann-Whitney rank sum test for pairwise difference (p < 0.005). When comparing each test group, only the
comparisons. The significance level for all statistical analyses was set ‘‘no-activation group’’ scored a 3 with a thin smear layer and showed
JOE — Volume -, Number -, - 2010 Final Irrigant Activation Protocols for Smear Layer Removal in Curved Canals 3
ARTICLE IN PRESS
Basic Research—Technology
Figure 2. A new fine-tuned scale used to evaluate sample cleanliness. Magnification: 1,000.
a statistical difference with the three other activation groups (p < 0.05) group, the ‘‘sonic group’’ (final irrigation + Endoactivator) showed
in which smear layer scores were always inferior to 3. a statistical difference compared with all the test groups (p < 0.05).
Comparisons between each group showed a statistically significant The exception was the ‘‘manual-dynamic activation group’’ (final irriga-
difference (p < 0.005) in the apical third. When comparing each test tion + gutta-percha agitation) in which no statistical diffence was
JOE — Volume -, Number -, - 2010 Final Irrigant Activation Protocols for Smear Layer Removal in Curved Canals 5
ARTICLE IN PRESS
Basic Research—Technology
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