Laser in Perio
Laser in Perio
Laser in Perio
* 200 Park Avenue South, Suite 1414, New York, NY 10003, USA.
E-mail address: [email protected]
0011-8532/04/$ - see front matter Ó 2004 Elsevier Inc. All rights reserved.
doi:10.1016/j.cden.2004.06.004
Box 1. Laser use in dentistry
Periodontics
Initial (nonsurgical) pocket therapy
Nonosseous gingival surgery
Frenectomy
Gingivectomy
Graft
Periodontal regeneration surgery
De-epithelialization
Removal of granulomatous tissue
Osseous recontouring
Fixed prosthetics/cosmetics
Crown lengthening/soft tissue management around abutments
Osseous crown lengthening
Troughing
Formation of ovate pontic sites
Altered passive eruption management
Modification of soft tissue around laminates
Bleaching
Implantology
Second-stage recovery
Peri-implantitis
Removable prosthetics
Epulis fissurata
Denture stomatitis
Residual ridge modification
Tuberosity reduction
Torus reduction
Soft tissue modification
Pediatrics/orthodontics
Exposure of teeth
Soft tissue management of orthodontic patients
Oral surgery/oral medicine/oral pathology
Biopsy
Operculectomy
Apicoectomy
Oral soft tissue pathologies
Operative dentistry
Deciduous teeth
Permanent teeth
R.A. Convissar / Dent Clin N Am 48 (2004) 771–794 773
Delivery systems
The field of lasers in general practice essentially began with the
introduction of the American Dental Laser (Birmingham, Michigan) dLase
300 neodymium:yttrium-aluminum-garnet (Nd:YAG) laser in 1990. Before
the introduction of this instrument, most dental lasers used bulky articulated
arms for their delivery systems. These articulated arms were not conducive to
the practice of general dentistry, owing to the long learning curve needed to
master their use and the difficulty of delivering the laser energy to the entire
oral cavity. Articulated arm delivery systems consist of a series of rigid
hollow tubes with mirrors at each joint (called a knuckle) that reflect the
energy down the length of the tube. These joints exist to allow the delivery
arm to be bent and configured in such a way as to bring the handpiece close
Fig. 1. Articulated arm delivery system. (Courtesy of DEKA Laser Technologies LLC, Ft.
Lauderdale, FL.)
774 R.A. Convissar / Dent Clin N Am 48 (2004) 771–794
to the target tissue. The laser energy exits the tube through a handpiece
(Fig. 1). Strauss [1] described the intraoral use of an articulated arm delivery
system. He stated that it is a difficult way to remove discrete lesions within the
oral cavity because of the awkward three-dimensional maneuverability of the
arm. A second problem with the use of articulated arms is the alignment of
the mirrors. To transmit the laser energy efficiently, the mirrors at each
knuckle must be aligned precisely. A misalignment of the mirrors could cause
a drop-off in the amount of energy transmitted to the handpiece. The mirrors
could go out of alignment through the normal use of moving the articulated
arm for each new procedure or if the laser is moved from treatment room to
treatment room. Articulated arm delivery systems are noncontact systems
(ie, the handpiece or its attachments do not come into contact with the target
tissue). Dentists are familiar with contact technology: The fissure bur
contacts the enamel during tooth preparation. The curet contacts the root
surface during scaling and root planing. The scalpel contacts the soft tissue
when incising. Using a technology in which there is no contact between the
instrument and target tissue can be challenging at first. This is one major
reason for a longer learning curve with these instruments compared with
contact technology instruments.
The American Dental Laser dLase Nd:YAG system was the first such
instrument to use a fiberoptic delivery system. This fiberoptic technology
allows for contact with the target tissue. The fiberoptic cables are attached to
a small handpiece similar in size to a dental turbine and are available in sizes
ranging from 200 lm in diameter to 1000 lm in diameter. Fiberoptic cables
also are relatively flexible. This flexibility allows for easy transmission of the
laser energy throughout the oral cavity, including into periodontal pockets.
Fiberoptic delivery and articulated arm systems are not the only two delivery
systems currently on the market. One manufacturer has developed a hollow
waveguide delivery system. In contrast to an articulated arm system, this
waveguide is a single long, semiflexible tube, without knuckles or mirrors. The
laser energy is transmitted along the reflective inner lumen of this tube and
exits through a handpiece at the end of the tube (Fig. 2). This handpiece comes
with various attachments that the dentist may select, depending on the
procedure to be performed, and may be used either in contact or out of contact
with the target tissue. Fig. 3 illustrates fiberoptic cables of various diameters
and handpieces from a carbon dioxide (CO2) waveguide delivery system.
The final delivery system is the air-cooled fiberoptic delivery system. This
type of delivery system is unique to the erbium family of lasers. A con-
ventional fiberoptic delivery system cannot transmit the wavelength of the
erbium family of lasers, owing to the specific characteristics of the erbium
wavelength. These special air-cooled fibers terminate in a handpiece with
quartz or sapphire tips. These tips are used slightly (1–2 mm) out of contact
with the target tissue.
Since the introduction of the dLase 300, general practitioners have seen
the number of wavelengths and manufacturers available to them increase
R.A. Convissar / Dent Clin N Am 48 (2004) 771–794 775
Fig. 2. Waveguide delivery system. (Courtesy of Opus Dent, Santa Clara, CA.)
Fig. 3. Fiberoptic cables of various diameters and handpieces from a CO2 waveguide delivery
system. (Courtesy of Robert Convissar, DDS, New York, NY.)
The coral pink and the melanotic gingiva would respond equally well to the
CO2 laser. Using the same patient models, gingivectomies performed with
the Nd:YAG and diode lasers would result in a significant difference in the
cutting efficiency. Diode and Nd:YAG lasers are absorbed preferentially by
tissue pigments, such as hemoglobin and melanin. The darker melanotic
gingiva would absorb the laser energy much more easily; it would cut more
quickly and easily than the coral pink gingiva. The melanotic tissue might
cut more rapidly than the clinician would like, possibly damaging the tissue
or creating a larger zone of thermal necrosis around the target tissue. In this
case, laser parameters (pulse duration, hertz, joules) would need to be
Table 1
Wavelengths currently available for sale in the United States
Wavelength Manufacturer Delivery system
Diode, 810–830 nm Biolase Fiberoptic cable
Hoya/Conbio Fiberoptic cable
Zap Lasers Fiberoptic cable
OpusDent Fiberoptic cable
Biolitec* Fiberoptic cable
Nd:YAG, 1064 nm Biolase Fiberoptic cable
Lares Research Fiberoptic cable
Millenium Dental Technologies Fiberoptic cable
Er:Cr:YSGG, 2780 nm Biolase Air-cooled fiberoptic/handpiece
Er:YAG, 2940 nm Hoya/Conbio Air-cooled fiberoptic/handpiece
OpusDent Hollow waveguide
CO2, 10,600 nm OpusDent Hollow wave guide
Deka Articulated arm
* The wavelength produced by the Biolitec laser is 980 nm; all other diode lasers produce
a wavelength of 810–830 nm.
R.A. Convissar / Dent Clin N Am 48 (2004) 771–794 777
Gingival surgery
According to statistics compiled by the American Dental Association,
dentists spend more time in the delivery of prosthetic care than any other
field except operative dentistry. The 2000 Survey of Dental Practice [2]
showed that the average general dentist spent 35.7% of his or her time in the
delivery of operative dentistry and 19% of his or her time in the delivery of
prosthetic care. A review of the procedures listed in Box 1 shows that most
of the laser procedures in fixed, removable, and implant prosthetics are
variations of the simple gingivectomy. The same may be said about most
soft tissue procedures in pediatric dentistry and many minor oral surgical
778 R.A. Convissar / Dent Clin N Am 48 (2004) 771–794
reached from this research is that diode and Nd:YAG lasers are safe and
effective wavelengths to be used in nonsurgical periodontal therapy when
used according to established protocols. As long as the laser energy is not
directed onto the root surface, wavelengths have been shown to be effective
instruments in nonsurgical periodontal therapy. This technique is discussed
in detail in the article on laser use for initial periodontal therapy. Fig. 4
illustrates a diode laser fiber being introduced into a periodontal pocket. The
fiber (slightly elongated for illustrative purposes) is parallel to the long axis of
the tooth, and the fiber tip does not come into contact with the root surface.
Fig. 4. Diode laser fiberoptic entering a periodontal pocket parallel to the long axis of the
tooth. (From Convissar RA. Lasers in general dentistry. Oral Maxillofac Surg Clin N Am
2004;16:165–79; with permission.)
782 R.A. Convissar / Dent Clin N Am 48 (2004) 771–794
Osseous resection
Many full-thickness mucoperiosteal flap procedures include osseous
resection. The only wavelengths cleared by the FDA for osseous surgery
are the erbium family of lasers. Er:YAG and Er:Cr:YSGG are the only
wavelengths that have the ability to ablate osseous tissue safely. There is
a great difference between FDA clearance for specific procedures, however,
and proof of efficacy when using lasers for those procedures. As addressed
earlier, the American Academy of Periodontology report [32] discusses the
fact that even though Er:Cr:YSGG has FDA clearance, peer-reviewed
literature defending its use for osseous procedures is lacking. In comparison,
the report does enumerate four articles in its discussion of the Er:YAG
wavelength, all of which led the American Academy of Periodontology to
state that the Er:YAG wavelength shows ‘‘the best application of laser use
directly upon hard tissue.’’ Four articles is hardly enough evidence to accept
unequivocally the role of this wavelength in osseous surgery. This is one area
of laser dentistry that needs more research. The role of lasers in osseous
surgery is discussed in more detail in the article on erbium lasers in this issue.
Endodontics
It is a well-accepted tenet of endodontic therapy that the cause of
periapical lesions and loss of tooth vitality is bacterial contamination.
Without the presence of bacteria, teeth do not lose vitality, and periapical
lesions do not develop. Spangberg [47] stated that the importance of infection
now is accepted as the major factor for the development of periradicular
inflammatory disease. Schilder [48] stated that the success of endodontic
treatment depends on the dentist’s ability to clean and disinfect the complex
canal system three dimensionally, then to fill and seal this space completely.
In a landmark study, Kakehashi et al [49] took normal rats and germ-free
rats and exposed their pulps. By day 8, all normal rats had nonvital, necrotic
pulps and periapical abscesses. The germ-free rats never lost pulp vitality. No
granulomas or abscesses formed. Dentinal bridges began to form by day 14,
with complete healing of the exposures by day 28, even with gross food
impaction in the endodontic access holes. Other studies have compared the
success rates of endodontically treated teeth with positive cultures with
endodontically treated teeth with negative cultures. Cultures were taken
immediately before obturation of the canals. The success rate of teeth with
negative cultures immediately before obturation was significantly higher
than the success rate of teeth with positive cultures [50,51].
Sundqvist et al [52] stated that most cases of endodontic failure are
thought to involve a continuing infection of the root canal system. Other
786 R.A. Convissar / Dent Clin N Am 48 (2004) 771–794
Fig. 5. Variety of endodontic attachments for the Er:Cr:YSGG laser handpiece. (Courtesy of
Biolase, San Clemente, CA.)
If bacteria are not removed from the tubules, this could lead to failure of the
endodontic treatment. Smear layer removal allows for superior cleaning and
sterilization of the root canal. Takeda et al [63] compared 17% ethyl-
enediaminetetraacetic acid (EDTA), a chelating solution commonly used in
endodontics to enlarge canals and remove the smear layer, with 6%
phosphoric acid and Er:YAG laser energy. Sixty extracted human teeth were
used in their study. The results showed that the Er:YAG laser was the most
effective in removal of the smear layer from root canal walls [63]. In
a separate study, Takeda et al [64] used 36 extracted teeth in a study to
evaluate further the use of Er:YAG lasers inside root canals. Their results
showed the Er:YAG laser–treated walls were free of debris, with open
dentinal tubules. Takeda et al [64] concluded that the Er:YAG laser
irradiation efficiently cleaned the root canal walls. A further study concluded
that Er:YAG lasers are effective in removing debris and the smear layer from
root canal walls [65]. When Er:YAG lasers were compared with other lasers,
notably argon and Nd:YAG lasers, the results showed that the Er:YAG laser
was the most effective wavelength and more effective than 17% EDTA in
removal of smear layer from root canal walls [66]. The sole remaining step in
endodontic therapy is the obturation of the canal. Er:YAG lasers have
shown a remarkable ability to enhance the results of the obturation process.
Application of Er:YAG energy to the root canal walls has been shown to
increase the adhesion of epoxy-based root canal sealers (AH26, AH Plus,
Topseal, Sealer 26, and Sealer Plus) to the canal walls. Pecora et al [67] used
99 extracted maxillary molars with an Instron Universal testing machine.
Their results showed that there was a statistically significant difference
between laser-treated dentin and EDTA-treated dentin with respect to
adhesion of sealer to the dentin walls [67]. Sousa-Neto et al [68] used 40
extracted human molars with an Instron Universal testing machine. Their
results showed that laser application significantly increased the adhesion of
root canal sealers. Research also has attempted to respond to the concerns of
laser energy flowing outside the root canal. One major concern would be the
effect of laser energy on the periodontal ligament surrounding the tooth, just
beyond the apex of the tooth. Research to date has concluded that the effects
on the periodontal ligament when using Er:YAG laser energy is minimal, and
no discernible effects on the periodontal ligament have been noted. Kimura
et al [69] irradiated 20 extracted human teeth with Er:YAG laser energy.
With the use of thermocouples and scanning electron microscopy, they
discovered that the root surface temperature did not increase significantly,
and there was no evidence of carbonization or melting.
All of this research involves the use of the Er:YAG laser wavelength of
2940 nm. The manufacturer of the Er:Cr:YSGG wavelength of 2780 nm has
suggested the use of their unit for complete endodontic therapy, including
instrumentation of the canal. This manufacturer has developed a series of
thin, flexible endodontic tips that may be used to enlarge the root canal. This
wavelength has been cleared by the FDA for endodontic instrumentation
R.A. Convissar / Dent Clin N Am 48 (2004) 771–794 789
Operative dentistry
Practically since the profession of dentistry began, dentists have been
seeking a method of removing decay painlessly and atraumatically without
affecting the surrounding healthy dental tissue. The field of laser operative
dentistry began with the FDA clearance of the Premier Laser Systems
Er:YAG laser for caries removal and cavity preparation in 1997. Since then,
three more erbium laser manufacturers have entered the market touting their
ability to remove diseased hard tissue without the need for anesthesia. These
lasers are indicated for all classifications of caries in enamel, dentin, and
cementum for deciduous and permanent teeth. Erbium lasers are capable of
removing not only decayed tooth structure, but also many nonmetallic
restorations. Defective composite, glass ionomer, and compomer restora-
tions may be removed quickly and easily without the use of analgesia. The
one limitation of use with erbium lasers is the removal of metallic and
porcelain restorations. Currently there is no laser that is able to remove
defective amalgam, gold, or porcelain restorations. These restorations must
be removed in a conventional manner before the laser may be used on the
tooth to remove the recurrent decay. It is beyond the scope of this article to
discuss in detail the process by which erbium lasers remove decay; this is
discussed in the article on erbium lasers elsewhere in this issue.
The erbium family of lasers are the only wavelengths that are indicated for
use in enamel, dentin, and cementum. For the sake of completeness, the
Nd:YAG laser was cleared for removal of first-degree caries in enamel in
1995; however, as a result of the limitations of its approval, its use in
operative dentistry is practically nonexistent today. The Nd:YAG laser has
been supplanted by the much more versatile erbium family. This family of
lasers consists of the Er:YAG laser with a wavelength of 2940 nm and the
Er:Cr:YSGG laser with a wavelength of 2780 nm. Although many dentists
790 R.A. Convissar / Dent Clin N Am 48 (2004) 771–794
are familiar with the name ‘‘Waterlase,’’ used to describe the Er:Cr:YSGG
wavelength, this is actually a misnomer. The statement that water plays a role
in the cutting ability of this laser compared with Er:YAG lasers, used in
advertising for this company’s products for years, is scientifically invalid.
Although the concept of ‘‘accelerated water’’ was proposed in 1994 by Riziou
and DeShazer [70], scientific studies have shown this not to be the fact.
Research by Fried et al [71] into the mechanism of Er:YAG and Er:Cr:YSGG
concluded unequivocally that the mechanism proposed by Riziou and
DeShazer [70] was incorrect. Hibst [72], using high-speed photography, also
concluded that there was no scientific basis for any evidence of a ‘‘hydro-
kinetic effect.’’ Freiberg and Cozean [73] concluded from their study of the
erbium family of lasers that if a hydrokinetic effect exists, it is not effective on
hard materials and does not contribute to enamel ablation.
Another significant difference is the absorption rate of these two
wavelengths in water and hydroxyapatite. Coluzzi [74] stated that the
Er:YAG wavelength has a 20% higher absorption in hydroxyapatite than
Er:Cr:YSGG. Hibst [72] stated that the absorption of Er:Cr:YSGG in water
is only half that of Er:YAG. Hibst [72] also compared Er:YAG and
Er:Cr:YSGG with the same operating parameters, the same optical fiber,
and the same spot size. He concluded that mass removal of dentin is greater
and pulpal temperature increase is smaller during laser drilling with
Er:YAG. Hibst [72] and Gimbel [75] also described multiple clinical trials
detailing the need for anesthetic during operative procedures with the
Er:YAG laser is only 2% to 10%. The author could find no similar peer-
reviewed studies using the Er:Cr:YSGG wavelength. Does this mean that
Er:YAG is superior biologically to Er:Cr:YSGG? It seems that there is
a stronger biologic rationale for the use of Er:YAG over Er:Cr:YSGG in
operative dentistry. The fact that Er:YAG causes less of a pulpal
temperature increase and removes more dentin per pulse than Er:Cr:YSGG
would lead one to that assumption; however, ‘‘wet-fingered’’ dentists put
a great deal of stock in clinical results they can see. The clinical results
dentists achieve with the Er:Cr:YSGG laser are within the bounds of
clinically acceptable results. Research is ongoing with other wavelengths
for hard tissue ablation. A new CO2 wavelength of 9.6 l is in development.
The frequency-doubled alexandrite laser also is under development. The
processes of development and testing of the alexandrite laser for dental use is
discussed in the article on laser research in this issue. For the present, the
Er:Cr:YSGG and Er:YAG lasers are clinically acceptable for use on dental
hard tissue.
Summary
When selecting a laser for a specific procedure, the dentist must consider
the interaction between the wavelength, target tissue, and surrounding tissue.
For many dental procedures, most soft tissue lasers produce excellent results.
R.A. Convissar / Dent Clin N Am 48 (2004) 771–794 791
References
[1] Strauss R. Laser management of discrete lesions in: laser applications in oral and
maxillofacial surgery. Philadelphia: WB Saunders; 1997.
[2] 2000 Survey of dental practice. Chicago: American Dental Association Publishing; 2001.
[3] Wigdor H, Walsh J, Featherstone JDB, Visuri S, et al. Lasers in dentistry. Lasers Surg Med
1995;16:103–33.
[4] Bader H. Use of lasers in periodontics. Dent Clin North Am 2000;44:779–92.
[5] Parkins F. Lasers in pediatric and adolescent dentistry. Dent Clin North Am 2000;44:
821–30.
[6] Ng V, Bissada N. Clinical evaluation of systemic doxycycline and ibuprofen administration
as adjunctive treatment for adult periodontitis. J Periodontol 1998;69:146–56.
[7] Asikainen S, Jousimies-Somer H, Kanervo A, et al. The immediate efficacy of adjunctive
doxycycline in treatment of localized juvenile periodontitis. Arch Oral Biol 1990;35:231–4.
[8] Lee W, Aitken S, Kulkarni G, et al. Collagenase activity in recurrent periodontitis: rela-
tionship to disease progression and doxycycline therapy. J Periodontol Res 1991;26:479–85.
[9] Jansson H, Bratthall G, Soderholm G. Clinical outcome observed in subjects with recurrent
periodontal disease following local treatment with 25% metronidazole gel. J Periodontol
2003;74:372–7.
[10] Rudhart A, Purucker P, Kage A, et al. Local metronidazole application in maintenance
patients: clinical and microbiologic evaluation. J Periodontol 1998;69:1148–54.
[11] Riep B, Purucker P, Bernimoulin J. Repeated local metronidazole therapy as an adjunct to
scaling and root planing in maintenance patients. J Clin Periodontol 1999;26:710–5.
[12] Latner L. Patient selection and clinical applications of periodontal tetracycline fibers.
Gen Dent 1998;46:58–61.
[13] Greenstein G. Treatiang periodontal diseases with tetracycline-impregnated fibers: Data
and controversy. Comp Cont Educ Dent 1996;16:448–55.
[14] Killoy WJ. Local delivery of antimicrobials: a new era in the treatment of adult periodontitis.
Comp Cont Educ Dent 1999;20(4 Suppl):13–8.
[15] Treatment of periodontitis by local administration of minocycline microspheres: a controlled
trial. J Periodontol 2001;72:1535–44.
[16] Dean JW, Branch-Mays GL, Hart TC, et al. Topically applied minocycline microspheres:
why it works. Comp Cont Educ Dent 2003;24:247–50.
[17] Van Steenberghe D, Rosling B, Soder P, et al. A 15 month evaluation of the effects of
repeated subgingival minocycline in chronic adult periodontitis. J Periodontol 1999;70:
657–67.
[18] Caton J. Evaluation of Periostat for patient management. Comp Cont Educ Dent 1999;20:
451–60.
[19] Caton JG, Ciancio SG, Blieden TM, et al. Treatment with subantimicrobial dose
doxycycline improves the efficacy of scalaing and root planing in patients with adult
periodontitis. J Periodontol 2000;71:521–32.
[20] Moritz A, Schoop U, Goharkhay K, et al. Treatment of periodontal pockets with a diode
laser. Surg Med 1998;22:302–11.
792 R.A. Convissar / Dent Clin N Am 48 (2004) 771–794
[43] Gregg RH, McCarthy DK. Laser periodontal therapy: case reports. Dent Today 2001;20:
74–81.
[44] Gregg RH, McCarthy DK. Laser ENAP for periodontal ligament regeneration. Dent Today
1998;17:86–9.
[45] Gregg RH, McCarthy DK. Laser periodontal therapy for bone regeneration. Dent Today
2001;21:54–9.
[46] Gregg RH, McCarthy DK. Laser ENAP for periodontal bone regeneration. Dent
Today 1998;17:88–91.
[47] Spangberg L. Endodontics today—a turn of the century reflection. Oral Surg Oral Med
Pathol Oral Radiol Endod 2000;89:659.
[48] Schilder H. Cleaning and shaping the root canal. Dent Clin North Am 1974;18:269–96.
[49] Kakehashi S, Stanley HR, Fitzgerald RJ. The effects of surgical exposures of dental pulps in
germ-free and conventional laboratory rats. Oral Surg Oral Med Oral Pathol Oral Radiol
Endod 1965;20:340–9.
[50] Heling B, Shapira J. Roentgenologic and clinical evaluation of endodontically treated teeth,
with or without negative cultures. Quintessence Int 1978;9:79–84.
[51] Zeldow B, Ingle J. Correlation of the positive culture to the prognosis of endodontically
treated teeth: a clinical study. J Am Dent Assoc 1963;66:9–13.
[52] Sundqvist G, Figdor D, Persson S, et al. Microbiologic analysis of teeth with failed
endodontic treatment and the outcome of conservative retreatment. Oral Surg Oral Med
Pathol Oral Radiol Endod 1998;85:86–93.
[53] Nair P, Sjogren U, Kreu G, et al. Intraradicular bacteria and fungi in root filled
asymptomatic human teeth with therapy-resistant periapical lesions: a long term light and
electron microscope follow-up study. J Endod 1990;61:580–8.
[54] Sjogren U, Hagglund B, Sundqvist G, et al. Factors affecting the long-term results of
endodontic treatment. J Endod 1990;16:498–504.
[55] Sjogren U, Figdor D, Persson S, et al. Influence of infection at the time of root filling on the
outcome of endodontic treatment of teeth with apical periodontitis. Int Endod J 1997;30:
297–306.
[56] MacDonald J, Hare G, Wood A. The bacteriologic status of the pulp chambers in intact
teeth found to be nonvital following trauma. Oral Surg Oral Med Oral Pathol Radiol
Endod 1957;10:318–22.
[57] Wittgow W, Sabiston C. Microorganisms from pulpal chambers of intact teeth with necrotic
pulps. J Endod 1975;1:168–71.
[58] Moritz A, Gutknecht N, Schoop U, et al. Irradiation of infected root canals with a
diode laser in vivo: Results of microbiological examinations. Lasers Surg Med 1997;21:
221–6.
[59] Gutknecht N, Moritz A, Conrads G, et al. Bactericidal effects of the Nd:YAG laser in vitro
root canals. J Clin Laser Med Surg 1996;142:77–80.
[60] Schoop U, Moritz A, Kluger W, et al. The Er.YAG laser in endodontics: results of an
in-vitro study. Lasers Surg Med 2002;30:360–4.
[61] Mehl A, Folwaczny M, Haffner C, et al. Bactericidal effects of 2.94 microns Er.YAG-laser
radiation in dental root canals. J Endod 1999;25:490–3.
[62] Fogel H, Pashley D. Dentin permeability: effects of endodontic procedure on root slabs.
J Endod 1990;16:442–5.
[63] Takeda FH, Harashima T, Kimura Y, et al. A comparative study of the removal of smear
layer by three endodontic irrigants and two types of laser. Int Endod J 1999;32:32–9.
[64] Takeda FH, Harashima T, Kimura Y, et al. Efficacy of Er.YAG laser irradiation in
removing debris and smear layer on root canal walls. J Endod 1998;24:548–51.
[65] Takeda FH, Harashima T, Eto J, et al. Effect of Er.YAG laser treatment on the root canal
walls of human teeth: an SEM study. Endod Dent Trauma 1998;14:270–3.
[66] Takeda FH, Harashima T, Kimura Y, et al. Comparative study about the removal of smear
layer by three types of laser. J Clin Laser Med Surg 1998;16:117–22.
794 R.A. Convissar / Dent Clin N Am 48 (2004) 771–794
[67] Pecora J, Cussioli A, Guerisoli M, et al. Evaluation of Er.YAG laser and EDTAC on dentin
adhesion of six endodontic sealers. Braz Dent J 2001;12:27–30.
[68] Sousa-Neto M, Marchesan M, Pecora J, et al. Effect of Er.YAG laser on adhesion of root
canal sealers. J Endod 2002;28:185–7.
[69] Kimura Y, Yonaga K, Yokoyama K, et al. Root surface temperature increase during
Er.YAG laser irradiation of root canals. J Endod 2002;28:76–8.
[70] Rizoiu I, DeShazer L. New laser matter interaction concept to enhance hard tissue cutting
efficiency. SPIE Proc 1994;2134A:309–17.
[71] Fried D, Ashouri N, Breunig T, et al. Mechanism of water augmentation during IR laser
ablation of dental enamel. Lasers Surg Med 2002;31:186–93.
[72] Hibst R. Lasers for caries removal and cavity preparations: state of the art and future
directions. J Oral Laser Applic 2002;2:203–12.
[73] Freiberg R, Cozean C. Pulsed erbium laser ablation of hard dental tissue: the effects of
atomized water spray vs. water surface film. SPIE Proc 2002;4160:74–81.
[74] Coluzzi D. An overview of laser wavelengths used in dentistry. Dent Clin North Am 2000;44:
753–66.
[75] Gimbel C. Hard tissue laser procedures. Dent Clin North Am 2000;44:931–54.