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Periodontology 2000, Vol. 48, 2008, 148–169  2008 The Author.

Printed in Singapore. All rights reserved Journal compilation  2008 Blackwell Munksgaard
PERIODONTOLOGY 2000

An overview of tooth-bleaching
techniques: chemistry, safety and
efficacy
M U N T H E R A.M. S U L I E M A N

Tooth discolouration results from varied and com- systems are based primarily on hydrogen peroxide or
plex causes that are usually classified as being either one of its precursors, notably carbamide peroxide,
intrinsic or extrinsic in nature. Extrinsic discoloration and are often used in combination with an activating
arises when external chromogens are deposited on agent such as heat or light. Bleaching agents can be
the tooth surface or within the pellicle layer. Intrinsic applied externally to the teeth (vital bleaching), or
discoloration occurs when the chromogens are internally within the pulp chamber (nonvital
deposited within the bulk of the tooth (usually in the bleaching) (41, 54). Both techniques aim to bleach
dentine) and are often of systemic or pulpal origin (1, the chromogens within the dentine, thereby changing
150). A third category of Ôstain internalizationÕ has the body color of the tooth.
been described to include those circumstances where
extrinsic stain enters the tooth through defects in the
tooth structure (1).
Tooth discoloration creates a wide range of cos-
Tooth discoloration
metic problems, and, as the dental profession and
Natural color of teeth
the public strive for a more esthetically pleasing
appearance, considerable amounts of time and Teeth are made up of many colors, with a natural
money are being invested in attempts to improve the gradation from the darker gingival third to the lighter
appearance of discolored teeth. A study assessing the incisal third of the tooth. This variation is affected by
impact of teeth on personal esthetic satisfaction the thickness and translucency of enamel and den-
found that dental variables (including tooth color) tine, as well as by the reflectance of different colors.
were more important than orthodontic variables, Typically, canine teeth are naturally darker than
suggesting that the appearance of the teeth was a central and lateral incisors and teeth become darker
greater contributing factor to an esthetic smile than with age, whereas lighter teeth are common in
their position within the arch (101). In another study, younger people, especially in the primary dentition.
of 254 patients, it was found that the appearance of The color of teeth is primarily determined by the
the dentition was more important to women than to dentine but is influenced by the color, translucency
men and that the esthetics of the dentition was more and varying degrees of calcification of enamel as well
important to younger patients (147). as its thickness, which is notably greatest at the
The methods available to manage discolored teeth occlusal or incisal edge. The normal color of teeth is
range from the removal of surface stain, bleaching or determined by the blue, green and pink tints of
tooth-whitening techniques and surgical techniques enamel and is reinforced by the yellow through to
to camouflage of the underlying discoloration, using brown shades of the dentine beneath.
veneers and crowns.
The use of a variety of bleaching techniques has
Classification of tooth discoloration
attracted most interest from the dental profession
because these techniques are noninvasive and rela- The appearance of teeth depends on their absorptive
tively simple to carry out. Contemporary bleaching or reflective properties of light and is influenced by

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An overview of tooth-bleaching techniques

Table 1. Colours produced by various causes of tooth


Metabolic causes of discoloration
discolouration A number of metabolic disorders, such as alkap-
Types of discolouration Colour produced tonuria, congenital erthropoietic porphyria and
Extrinsic (direct stains) congenital hyperbilirubinemia, cause tooth discol-
Tea, coffee and other foods Brown to black oration. Alkaptonuria is an inborn error of metabo-
Cigarettes ⁄ cigars Yellow ⁄ brown to black lism that results in a brown discoloration of the
Plaque ⁄ poor oral hygiene Yellow ⁄ brown permanent dentition (79), whereas congenital
Extrinsic (indirect stains) erythropoietic porphyria, a rare, recessive, autoso-
Polyvalent metal salts and Black and brown
mal metabolic disorder, gives a red ⁄ purple–brown
cationic antiseptics
(e.g. chlorhexidine) discoloration of teeth (37). Congenital hyperbiliru-
Intrinsic binemia is characterized by yellow–green discolor-
Metabolic causes ation caused by the deposition of bile pigments in
(e.g. congenital Purple ⁄ brown calcifying dental hard tissues, particularly at the
erythropoietic porphyria) neonatal line, as a result of massive hemolysis in
Inherited causes Brown or black
rhesus incompatibility.
(e.g. amelo ⁄
dentinogenisis) Banding appearance
Iatrogenic causes
Tetracycline Classically yellow, brown, Inherited causes of discoloration
blue, black or grey
Fluorosis White, yellow, grey or black Amelogenesis imperfecta is a hereditary condition
Traumatic causes Brown in which the mineralization or matrix of enamel
Enamel hypoplasia Grey black formation is disturbed. There are currently 14 dif-
Pulpal haemorrhage Pink spot ferent subtypes based on clinical appearance, with
products
Root resorption Yellow
the majority inherited as an autosomal-dominant or
Ageing causes X-linked trait with varying degrees of expressivity
Internalized (139, 158, 160). The appearance can be badly
Caries Orange to brown affected with hypoplastic thin enamel that is yellow
Restorations Brown, grey, black to yellow–brown in color or the enamel can be quite
mildly hypomineralized (Ôsnow-cappedÕ), depending
on the type of amelogenesis imperfecta present.
all the structures that make up the tooth, including The color of the teeth is presumed to reflect the
the enamel, dentine and pulp. Any changes to these
degree of hypomineralization of the enamel: the
structures during formation or throughout develop-
darker the color the more severe the degree of
ment and post-eruption (3 months in utero to 20
hypomineralization (18).
years) can cause a change in the light-transmission Dentine defects can either be inherited or caused
properties and hence discoloration. by environmental factors (120). Genetically deter-
Table 1 shows the types of tooth discoloration and
mined defects may occur in isolation or may be
the typical tooth colors they produce.
associated with a systemic disorder.
Dentinogenesis imperfecta is an inherited disorder
of dentine, which may or may not be associated
Intrinsic discoloration with osteogenesis imperfecta (18). Dentinogenesis
imperfecta type I is associated with osteogenesis
Intrinsic discoloration occurs following a change to imperfecta (mixed connective tissue disorder of type
the structural composition or thickness of the den- I collagen) and is characterized by opalescent pri-
tinal hard tissues during tooth development. mary teeth, especially when the condition is the
This classification can be further subdivided into result of a dominant inheritance pattern. Dentino-
the following categories: genesis imperfecta type II or hereditary opalescent
• metabolic causes. dentine may be more severe in the primary than in
• inherited causes. the secondary dentition, the pulp chambers often
• iatrogenic causes. become obliterated and the dentine undergoes rapid
• traumatic causes. wear once the enamel has chipped away. Clinically,
• idiopathic causes. the appearance is an amber, grey to purple–blue
• ageing causes. discoloration or opalescence, thought to be a result

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of the absorption of chromogens into the porous • degree I: there is minimal expression of tetracy-
dentine after exposure of the dentine. This condition cline stain, which is uniformly confined to the
is clearly demonstrated by opalescence on trans- incisal three-quarters of the crown and is light
illumination. yellow in color.
Unlike dentinogenesis imperfecta type II, denti- • degree II: there is more variability in staining,
nogenesis imperfecta type I shows enamel that is ranging from a highly uniform deep yellow to a
much less prone to fracture and the dentine seldom grey-banded discoloration in which a distinctive
obliterates pulp chambers; hence, radiographic difference in discoloration is noted between the
examination can differentiate between the two types. cervical region and the incisal four-fifths of the
A third type of dentinogenesis imperfecta has been crown.
described (157) that is similar in appearance to • degree III: there is very dark blue or grey uniform
dentinogenesis imperfecta types I and II but with the discoloration.
radiographic appearance of Ôshell teethÕ with multiple Post-eruptive staining with minocycline used for the
pulpal exposures in the primary dentition. treatment of acne in adolescents and adults has been
There is some controversy as to whether dentinal described as a result of chelation with iron to form
dysplasias are a separate entity from dentinogenesis insoluble complexes (14) or by the formation of
imperfecta (18). The primary and secondary denti- complexes of the drug with secondary dentine (117).
tions in type I dentinal dysplasia are of normal Fluorosis may be the result of the natural occurrence
shape and form but have an amber translucency. of fluoride in water supplies or from fluoride in
The pulp chambers in the primary dentition are mouthrinses, tablets or toothpastes. This type of
frequently obliterated while only crescentic pulpal staining is most often confined to the enamel, varying
remnants are found parallel to the cemento–enamel from areas of flecking to diffuse opaque mottling
junction of the secondary dentition. Type II dentinal superimposed onto a chalky white or dark brown–
dysplasias are thought to involve thistle-shaped pulp black background. The dark discoloration is thought to
chambers and pulp stones with a brown tooth dis- be post-eruptive by a process of internalization of
coloration (126). extrinsic stain into the porous enamel (151). The
severity of the discoloration is related to the age and
dose administered and can affect both the primary and
Iatrogenic causes of discoloration
secondary dentitions in endemic cases of fluorosis.
Tetracycline staining results from systemic adminis-
tration of the drug and its subsequent chelation to
Traumatic causes of discoloration
form complexes with calcium ions on the surface of
hydroxylapatite crystals primarily within dentine, al- One of the most common causes of tooth discolor-
though enamel is also affected (140). Tetracycline ation seen in everyday general practice is that caused
should be avoided in expectant and breast-feeding by pulpal hemorrhagic products following trauma.
mothers, and in children up to the age of 12 years, to The major cause of the discoloration is thought to be
avoid discoloration of the developing teeth. The dis- the accumulation of the hemoglobin molecule or
coloration produced depends on the type of tetracy- hematin molecules in the traumatized tooth, and
cline used, the dosage and the period of time for their penetration into the dentine determines the
which it is taken, as well as the age of the patient at severity of the discoloration.
the time of administration. Generally, the affected Root resorption following trauma often presents as
teeth tend to be yellow or brown–grey in color and a pink spot lesion at the cemento–enamel junction in
the appearance is worse on eruption and diminishes an otherwise symptomless tooth. The resorption al-
with time. This is because once erupted the teeth are ways begins at the root surface but may be internal
susceptible to color changes by photo-oxidation (of pulpal origin) or external (of periodontal origin).
(exposure to light), causing lightening of the intrinsic Enamel hypoplasia in permanent teeth may be the
stain. Various analogues of tetracycline produce dif- result of disturbance of the developing tooth germ
ferent color changes, for example, chlorotetracycline following trauma or infection of the deciduous tooth,
produces a slate-grey color, and a creamy discolor- giving rise to a localized enamel defect. Pitting or
ation is produced by oxytetracycline (10, 94). grooving may predispose to later internalization of
Tetracycline staining has also been classified external chromogens. Generalized hypoplasia may
according to the extent, degree and location of the result from any disturbance of the developing tooth
tetracycline involvement (64). germ by many different fetal or maternal conditions,

150
An overview of tooth-bleaching techniques

such as rubella infection or even drug intake during into the pellicle layer and producing a stain as a result
pregnancy. The defect is usually directly related to of the basic color of the chromogens; and indirect
the degree of the systemic upset and can be chro- staining where there is chemical interaction at the
nologically traced back to the time of the upset. tooth surface with another compound that produces
Dentine hypercalcification may result following the stain.
trauma temporarily disturbing the blood supply of a
tooth and affecting the odontoblasts, giving rise to
Direct staining
excessive irregular dentine deposition in the pulp
chamber and canal walls. The tooth gradually Direct-staining chromogens derived from dietary
decreases in translucency and becomes yellow or sources such as tea and coffee are taken up into the
yellow–brown in color but is still vital (113). pellicle and their natural color imparts the stain onto
the tooth surface. Smoking or chewing tobacco,
medicines, spices, vegetables and red wine are also
Idiopathic causes of discoloration
known to cause direct staining. It is the polyphenolic
Molar incisor hypomineralization is a condition of compounds found in food that are thought to give
unknown etiology that is characterized by severely rise to the color of the stain (105). The actual mech-
hypomineralized enamel affecting the incisors and anism of staining is not fully understood but certainly
permanent first molars (154). The appearance of the involves pellicle constituents. Naked enamel does not
hypomineralized enamel is asymmetrical, affecting take up chromogens easily and pellicle proteins are
one molar severely while leaving the contralateral often cited as reacting with chromogens, but how
molar relatively unaffected or only with minor sub- specific this reaction is has not been clarified and
surface defects (152). The incisors also show asym- some degree of nonspecificity is probable; the chro-
metry but not usually with loss of enamel substance. mogen is merely incorporated within the pellicle
The enamel defects can vary from white to yellow or layer much as a sponge can soak up and hold fluids.
brownish areas, but they always show a sharp de- Dentine chromogens may be absorbed into the tissue
marcation between sound and affected enamel (153). itself as dentine is more porous than enamel, both in
The enamel is porous and brittle, breaking down respect of intertubular dentine and the tubules
shortly after eruption under masticatory forces, and themselves (125).
often resembles enamel hypoplasia but is distin- Traditionally, extrinsic tooth discoloration has
guished by having irregular borders with normal en- been classified according to its origin and whether it
amel as opposed to smooth borders with hypoplastic is metallic or nonmetallic (47).
lesions (153). Nonmetallic extrinsic stains caused by beverages,
The suggestions of possible etiologies for molar tobacco, mouthrinses and other medicines are ad-
incisor hypomineralization include environmental sorbed on to the tooth surface by incorporation into
changes during a limited time period, infections the plaque or the acquired pellicle. Chromogenic
during early childhood, dioxin in breast milk and bacteria have also been implicated in extrinsic
genetic factors. staining in children who have poor oral hygiene
(causing green and orange stains) and in those who
have good oral hygiene (causing black–brown stains)
Ageing causes of discoloration
but the mechanism involved has not been estab-
The natural darkening and yellowing of teeth with age, lished (150).
and the change in their light-transmission properties,
is the result of a combination of factors involving both
Indirect staining
enamel and dentine. The enamel undergoes both
thinning and textural changes (96), while the deposi- Indirect dental stains are associated with cationic
tion of secondary and tertiary dentine and pulp stones antiseptics and metal salts that are either colorless or
all contribute to the darkening process of ageing. a different color from the stain produced as a result of
a chemical interaction with another compound.
Polyvalent metal salts are known to be associated
Extrinsic discoloration with extrinsic staining, such as the black discolor-
ation seen in people using iron supplements and in
External staining may be divided into two main cat- iron foundry workers exposed occupationally to these
egories: direct staining by compounds incorporated metal salts. Other examples include the green dis-

151
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coloration resulting from use of mouthrinses con- silver points in root canals give a grey or pink
taining copper salts or the violet–black color resulting appearance to a root-treated tooth.
from the use of potassium permanganate-containing
mouthrinses (149).
Cationic antiseptics, such as chlorhexidine, hexe- Development of night guard vital
tidine, cetylpyridinium chloride and others mouth- bleaching
rinses, also cause staining after prolonged use.
Chlorhexidine, for example, produces the brown– A successful home bleaching technique using
black discoloration seen around the labial and lingual hydrogen peroxide was first described by Klusmier in
surfaces of anterior teeth after only about 7–10 days 1968 (52) when it was noticed that teeth became
of use. whiter after treatment of a mouth injury with Gly-
The mechanism of staining by metal salts, and oxide (hydrogen peroxide mouthwash) in an ortho-
particularly by cationic antiseptics, has attracted dontic retainer. The results were lighter teeth in
much interest from the dental profession and has addition to healing of the injury. However, this
been much debated (1, 150). The majority of the data technique received worldwide acceptance when de-
drawn from randomized controlled laboratory and scribed in 1989 by Haywood & Heyman (53), who
clinical studies support a dietary etiology. Thus, employed 10% carbamide peroxide in a custom-
staining is thought to be a result of the precipitation made tray worn at night: the Ônight guard vital
of anionic dietary chromogens, such as polyphenols, bleaching techniqueÕ (53).
onto adsorbed cationic antiseptics or polyvalent
metal salts on the tooth surface (1, 150).
Development of power bleaching
Internalized discoloration In-surgery bleaching techniques used since the early
1900s were further modified in 1991 with the intro-
Extrinsic stains are taken up into the enamel or duction of 30% hydrogen peroxide gels activated by
dentine via a developmental or acquired defect. The conventional light-curing units rather than a heat
incorporation of extrinsic stain into the porous tooth source. This technique is often referred to as Ôpower
structure of developmental defects has already been bleachingÕ. Although these power gels could be con-
discussed under the intrinsic staining section above. trolled easily compared with the liquids used previ-
Acquired defects of teeth resulting from function ously, full-mouth isolation was still needed to protect
and parafunction, dentinal caries and restorative the gums and the surrounding soft tissues. Power
materials can all lead to tooth discoloration, directly bleaching was frequently combined with home-use
or indirectly. tray systems to maximize the bleaching effect and
• tooth wear and gingival recession: the loss of en- give a kick start to the whitening procedure before the
amel and dentine by erosion, abrasion and attrition patient continued with night guard vital bleaching at
can result in the exposure of dentine to extrinsic home.
chromogens. The exposure of dentine, or the loss A further modification to the power bleaching
of enamel, gives rise to darker looking teeth as system was the use of an argon laser as an activating
more of the yellow color of dentine is apparent. light source to replace conventional curing lights
Cracks as a result of trauma to the enamel, or (110). The present-day systems are activated by a
gingival recession and exposure of dentine, pre- variety of light sources: plasma arc lamps, Xenon-
dispose the teeth to extrinsic stain internalization. halogen, light emitting diode (LED) light and diode
• dentinal caries: the progression of the carious le- lasers. However, light sources are not essential and
sion is usually associated with changes in color, there are systems that require chemical activation
ranging from the initial white spot lesion to the only and are merely painted onto the teeth with the
black arrested lesion that picks up stain from an usual use of gingival and mucosal isolation (22).
extrinsic source (145).
• restorative materials: the classic grey–black dis-
coloration seen around old amalgam restorations Current bleaching materials
is thought to be caused by the migration of tin into
the dentinal tubules (155). Eugenol-containing The home bleaching materials currently available are
medictions cause an orange–yellow stain, and a combination of different concentrations and fla-

152
An overview of tooth-bleaching techniques

vours of both carbamide peroxide or hydrogen per-


Bleaching chemistry
oxide used in either custom-made trays or Ôone size
fits allÕ type trays. In addition to these are the rela- Hydrogen peroxide acts as a strong oxidizing agent
tively new hydrogen peroxide gels on polyethylene through the formation of free radicals, reactive oxy-
strips (Whitestrips; Procter & Gamble, Cincinnati, gen molecules and hydrogen peroxide anions (32).
OH, USA), which are applied like medical plasters These reduce or cleave pigment molecule double
onto the surface of the labial tooth and lap over the bonds to either break down pigments to small en-
incisal edges of the teeth. Other over-the-counter ough molecules that diffuse out of the tooth or to
bleaching agents include paint-on carbamide perox- those that absorb less light and hence appear lighter.
ide preparations of various concentrations used in a Such pigmented molecules tend to be organic, al-
similar way to the bleaching strips. Disposable trays though inorganic molecules can be affected by these
that are prefilled with 9% hydrogen peroxide with reactions.
inbuilt gingival protection have recently been intro- Hydrogen peroxide forms a loose association with
duced (Ultradent Products Inc., South Jordan, UT, urea to produce urea peroxide (carbamide peroxide),
USA). which is easily broken down in the presence of water
Glycerine-based home bleaching solutions have to release free radicals that penetrate through the
now been largely replaced because they dehydrate enamel pores and into the dentine to produce the
the tooth, increasing the risk of thermal sensitivity. bleaching effect. The urea can theoretically be further
Less viscous solutions of both hydrogen peroxide and decomposed to carbon dioxide and ammonia, which
carbamide peroxide are now available that are ap- elevates the pH to facilitate the bleaching procedure
plied for shorter time periods, but their low viscosity further (138). This can be explained by the fact that,
may lead to leakage onto the gingivae, increasing the in a basic solution, lower activation energy is re-
potential gingival irritation (76). quired for the formation of free radicals from
The Ôdeep bleaching techniqueÕ has recently be- hydrogen peroxide, and the reaction rate is higher,
come popular among the profession, with its pro- resulting in an improved yield compared with an
claimed predictability of shade B1 (Vita, Zahnfabrik, acidic environment (27).
Germany) results for every patient. This technique The breakdown of hydrogen peroxide into free
involves night guard vital bleaching for 14 nights radicals is summarized in Fig. 1.
using 16% carbamide peroxide in specially made Stains caused by inorganic substances locked into
trays that is followed, on the 15th day, by a 1-h in- the crystal lattice of the enamel structure, or held
surgery power bleaching session using 9% hydrogen superficially by salivary protein interactions, require
peroxide in the same trays. The manufacturers the oxidation of the sulphide or thiolate bonds via
claim that the home bleaching conditions the teeth suitable catalysts, such as Fe(II), before they are
by increasing their permeability so that the in-sur- receptive to bleaching agents. Often these catalysts
gery procedure is a lot more effective. The trays are are either unavailable or in short supply, causing the
made by first taking impressions in metal trays degradation of hydrogen peroxide to proceed very
using a medium-bodied silicone for greater accu-
racy. The reservoirs on the trays are made by adding
a colored stone to the cast models instead of the A
resin usually used in this procedure. This, coupled H2O2 2HO·
with the use of a greater force ⁄ pressure in the
vacuum moulding machine, gives rise to a better HO· + H2 O2 H2O + HO·2
seal to the bleaching tray about 1 mm below the
HO·2 H + O·2
+
gingival margin. It is this better sealing of the tray,
enabling the bleaching agent to be active all night, B
which is believed to be key to the procedure. In
2 H2O2 2H2O + 2{O} 2H2O + O2
addition, the patient must continue with the home
bleaching for 14 consecutive days and, to reduce the C
inevitable sensitivity, the patient is given a desen- H2O2
+ -
H + HOO
sitizing agent containing benzalkonium chloride and
Fig. 1. Hydrogen peroxide forms free radicals like hydroxyl
fluoride. There is no scientific evidence yet available and perhydroxyl radicals and superoxide anions (A),
to support the claims made regarding this tech- reactive oxygen molecules that are unstable and trans-
nique. formed to oxygen (B), and hydrogen peroxide anions (C).

153
Sulieman

slowly, and therefore extended treatment times are 13, 89, 123). Adverse effects reported by frequency for
usually required for these stains (103). all home bleaching products show that 27% of pa-
The perhydroxyl (HO2•) free radical is thought to be tients suffer an unpleasant taste and a further 27%
the most reactive species in tooth bleaching, the complain of a burning palate sensation. Other ad-
formation of which is favoured by high pH, but this is verse effects included burning throat or gingival tis-
rarely the situation as the product shelf life is sues, gingival ulceration and tooth sensitivity (60). All
adversely affected under these conditions. Although such ill effects usually resolve on cessation of treat-
the perhydroxyl free radical is a very reactive species, ment.
it does need metal trace elements in the mouth to A number of studies have reported an increase in
catalyse its action. gingival health following bleaching procedures (109)
With use of both carbamide peroxide and hydrogen and two reasons have been put forward for this. The
peroxide the teeth should ideally be dry and free of first is that the bleaching solution is toxic to the
debris because enzymes and proteins found in saliva bacteria within the gingival crevice (8) and the sec-
are capable of catalyzing the nonbleaching break- ond is that patients undergoing bleaching might take
down of peroxides to water and oxygen. more interest in their teeth and as a result may
In addition to their use in nonvital bleaching improve their oral hygiene during the treatment.
techniques, perborates in gel form, very much like
carbamide peroxide, have been used for tray-applied
Tooth sensitivity
vital bleaching. However, when dispatched in powder
form, perborates can be incorporated into a paste The sensitivity of teeth in some individuals during
after mixing with water, saline or hydrogen peroxide bleaching is a problem that has attracted little re-
and placed in the pulp chambers of nonvital teeth. search attention, even though two-thirds of patients
Sodium perborate is stable when in the form of a dry generally experience sensitivity during home
powder but in the presence of acid, moist air or water bleaching, which usually lasts between 1 and 4 days
it decomposes to form metaborate, hydrogen per- (67, 99, 112, 119). However, a number of studies have
oxide and nascent oxygen (Fig. 2). Hydrogen peroxide assessed the occurrence of the sensitivity relative to
mixed with sodium perborate potentiates its effect its time of onset and duration of the symptoms. The
and is believed to produce a better bleaching effect incidence of sensitivity ranges from 11 to 93% of
(103, 114), although no evidence to support this is patients using 10% carbamide peroxide (32, 71, 73,
available. These compounds have also been shown to 79) and the average first report of sensitivity was after
remove chlorhexidine-induced extrinsic stain both 4.8 days (±4.1 days), usually lasting for 5 days (±3.8
in vitro and in vivo (2). Other products marketed as days) (142).
peroxide-free bleaching agents employ an oxygen Tooth sensitivity is believed not to relate to ex-
complex made up of a mixture of sodium perborate, posed root surface or dentine or caries, but instead is
sodium chlorite and oxygen. explained by the easy passage of the hydrogen per-
oxide molecules through the enamel and dentine into
the pulp (50). This results in pulpal inflammation
Bleaching safety
affecting the pulpal sensory nerves that trigger in
A number of authors have investigated the safety of response to stimuli, such as cold drinks, until the
bleaching procedures (11–13, 22, 28, 60, 61, 66–69, 73, inflammation subsides. However, dentine exposure
89, 90, 97, 118, 122, 123, 131, 162) but have tended to may be a factor in tooth sensitivity as it is often
concentrate mainly on the use of carbamide peroxide misdiagnosed as not being present clinically (9). In
used in at home bleaching systems (11, 13, 28, 60, 66– fact, other workers (65) have correlated the incidence
69, 89, 90, 97, 118, 122, 123, 162). The evidence on and severity of thermal sensitivity with gingival
safety published to date on the whole tend to suggest recession and the frequency, not actual duration, of
that bleaching is a relatively safe procedure (28, 60, the treatment (76).
61, 67–69, 73, 90, 97, 122, 131, 162) but some workers Risk factors for the development of tooth sensitivity
have voiced concerns about potential structural and gingival irritation that are associated with night
changes that may occur as a result of bleaching (11– guard vital bleaching were reported by Leonard et al.
(74). No statistical relationship existed between age,
Na2[B2(O2)2 (OH)4 ] + 2H2O 2Na BO3+ 2H2O2 gender or tooth characteristics, with the dental arch
Fig. 2. The formation of hydrogen peroxide from sodium bleached and the development of side effects. Ini-
perborate. tially, a statistically significant association existed

154
An overview of tooth-bleaching techniques

between the side effects and the whitening solution leads to the sensation of pain. Histological changes to
used. However, when the analysis was controlled for the pulp after night guard vital bleaching with 10%
usage pattern, this relationship disappeared. Patients carbamide peroxide have recently been reported to
who changed the whitening solution more than once be minor; they did not affect the overall health of the
a day reported more statistically significant side pulp tissue and were reversible within 2 weeks post-
effects than did those who did not change the treatment (40). In a previous study in which the pulps
whitening solution during their usage time. were evaluated after overnight bleaching with 10%
Schulte et al. (119) reported on a clinical study carbamide peroxide for either 4 or 14 days, mild
involving the use of 10% carbamide peroxide on 28 inflammatory changes were demonstrated in four out
people. Four subjects discontinued bleaching because of 12 teeth, irrespective of treatment duration (46).
of thermal sensitivity, whereas the remainder showed However, in those teeth treated for 14 days, followed
no change in pulpal readings recorded before the start by a rest period of 14 days, no inflammation was
of the treatment and at any time during the study. detected.
Sterrett et al. (129) found that all the individuals In a clinical study monitoring post-operative dis-
experienced mild, transient sensitivity during a 3- comfort associated with vital bleaching, Nathonson &
week trial. However, the consensus view from other Parra (99) found that 30% of patients had no sensi-
trials was that two-thirds of patients experienced tivity, whereas the majority of the others only expe-
mild, transient thermal sensitivity, which disap- rienced mild symptoms lasting less than 24 h, with
peared on the cessation of bleaching (67, 99, 112, patient age having no effect on the degree of sensi-
119). The penetration into the pulp of various com- tivity experienced. This was contrary to the widely
mercially available 10% carbamide peroxide bleach- held view that younger patients with wider pulp
ing products has been shown to differ significantly horns would develop more sensitivity.
and may therefore account for the varying levels of The efficacy of desensitizing agents used in pa-
sensitivity reported (144). tients who experience tooth sensitivity during tooth
Although there is a widely held belief that higher whitening has been reported in a study of such pa-
concentrations of bleaching agents produce a greater tients who had pre-existing symptoms prior to the
prevalence of tooth sensitivity, studies reported start of the whitening procedure (76). This study
disprove this theory (68, 86). suggested that the use of a 3% potassium nitrate and
Cohen & Parkins (24) monitored vital bleaching for 0.11% fluoride desensitizing agent for 30 min prior
six children with tetracycline-stained teeth involving to whitening may decrease tooth sensitivity when
heat and hydrogen peroxide application for eight compared with a placebo gel.
consecutive 30-min sessions at 1-week intervals. Pre-
treatment and post-treatment vitality tests were
Effects on the pulp
performed on test and control teeth, and no changes
in vitality were found throughout the study. A study of the penetration of hydrogen peroxide re-
Cohen (23) also attempted to relate the prevalence ported that the compound enters readily through the
of tooth sensitivity in vital bleaching with possible enamel and dentine to reach the pulp chamber of
histological pulpal changes. The study involved 19 extracted teeth (16). Bowles & Thompson (15) have
patients in whom 51 premolars were bleached with shown that hydrogen peroxide concentrations as low
35% hydrogen peroxide and heat in 30-min sessions. as 5% can dramatically inhibit pulpal enzyme activity.
All test and control teeth were extracted for ortho- These enzymes were quite sensitive to the combina-
dontic reasons and subsequently histologically tion of hydrogen peroxide and heat, but the quantities
examined. Of the patients treated, 78% experienced required to produce this inhibitory effect were in the
some form of sensitivity, lasting for 24 h, from region of 50 mg. A follow-up study then went on to
bleaching; in one individual the discomfort lasted for show that although dental hard tissues exhibited
48 h. Histological findings from the study showed substantial permeability to hydrogen peroxide, espe-
that all pulps were normal except for moderate cially with the application of heat, the quantities that
vasodilation and aspiration of odontoblast nuclei into diffuse into the pulp chamber were in the order of only
the dental tubules, which was found to occur with micrograms: too low to produce inhibitory effects on
equal frequency in both test and control teeth. Cohen enzymes and therefore unable to cause permanent
(23) concluded that sensitivity and discomfort during pulpal damage (16). The effects of carbamide peroxide
and after bleaching procedures are caused by heat penetration were also studied and it was found that
application increasing the intrapulpal pressure that for the same effective concentration, there was less

155
Sulieman

penetration of the pulp from carbamide peroxide than hardness and fracture resistance of enamel (13, 89).
from free hydrogen peroxide (26). Bleaching does not cause any perceptible etching of
The effects of light-enhanced bleaching on the the teeth, and morphological changes in the outer 25
in vitro surface and on intrapulpal temperature rise lm of the enamel are clinically insignificant (90, 146).
have been reported (4, 134, 137). Baik et al. (4) inves- Abrasion, erosion, surface hardness and morphologi-
tigated the effect of the presence, absence and ageing cal changes of enamel and dentine following power
of heat-enhancing colorant added to the bleaching gel bleaching using 35% hydrogen peroxide were inves-
on the temperature rise of the gel itself, as well as on tigated (131). There were no significant changes
the temperature rise within the pulp chamber, when a following the bleaching procedure as the high con-
tooth was exposed to a variety of lights. The results centration of hydrogen peroxide did not affect the
showed that the freshness of this bleaching agent abrasion, erosion or hardness of both enamel and
influences the temperature rise of the bleaching gel dentine. One possible reason for the reported delete-
and may also increase the intrapulpal temperature. rious effect on enamel and ⁄ or dentine of bleaches is
Use of the lights elevated the bleach temperature, not the bleach itself but the pH of the formulation
which resulted in an increased intrapulpal tempera- used. The pH of various commercially available tooth-
ture that may further impact on patient sensitivity and whitening agents was analysed in a study by Price et
pulpal health. A variety of different bleaching lights, al. (108) who found the range was from highly acidic
including a diode laser, were investigated by Sulieman (pH 3.67) to highly basic (pH 11.13), with the over-the-
et al. (134, 137) who found that these lights did not counter preparations having a significantly different
increase the intrapulpal temperature above the critical pH to both the at-home and in-surgery bleaching
5.5 C (161) as long as they were used within the materials. The over-the-counter bleaching agents
manufacturersÕ guidelines. have been found to have very acidic pH values, which
may cause erosion of the enamel, and the toothpastes
supplied with them can be quite abrasive (62).
Root resorption
There may be a loss of organic components from
Cervical resorption is seen occasionally in bleached, bleached enamel and dentine surfaces. The cal-
root-filled teeth and has been attributed to a combi- cium:phosphate ratio of dentine was found to be
nation of trauma and bleaching with high-concen- significantly reduced by bleaching with 30% hydro-
tration hydrogen peroxide (30%) and heat (39). gen peroxide and 10% carbamide peroxide in a study
Heithersay et al. (57, 58) studied the radiographs and by Rotstein et al. (115). In another study, by
records of 204 teeth from 158 patients who had re- McCraken & Haywood (90), teeth exposed to 6 h of
ceived tooth-bleaching treatment in a specialist end- bleaching using carbamide peroxide lost an average
odontic practice in the past 1–19 years. Seventy-eight of 1.06 lg ⁄ mm2 of calcium, which was found to be
per cent of these teeth had prior incidents of trau- similar to the amount lost from the enamel after a
matic injury. All teeth were bleached using a combi- 2-min exposure to carbonated cola, orange juice or
nation of thermocatalytic or heat-activated 30% carbonated diet cola (48). The potential for reminer-
hydrogen peroxide and walking bleach techniques. alization in vivo could counteract these effects but to
Only four of these teeth (2%) had developed invasive date this has not been investigated.
cervical resorption during the review period, which Bleaching has no effect on the erosion and
might have been a result of the original trauma. demineralization of enamel (17, 80, 106, 123), but the
methods of assessment have been debated as mi-
crohardness has often been the sole method of
Effects on physical properties measurement. The argument is that measuring only
the softened portion of the lesion is unable to
Scanning electron microscopy of enamel bleached quantify the bulk loss of tissue, which would require
with carbamide peroxide showed little or no change in assessment methods such as profilometry.
morphology (55), whereas other work showed areas of
shallow erosions (54) or more substantial changes in
enamel structure (11, 12, 123). Surface hardness and Effects on enamel ⁄ dentine
wear resistance has also been investigated with results bonding
showing a lack of agreement on the overall effect of
bleaching. The results range from no effect on tooth- Bonds to enamel ⁄ dentine may be altered following
wear (70, 73, 156) to a significant decrease in the bleaching because of the presence of hydrogen

156
An overview of tooth-bleaching techniques

peroxide. Resin tags in bleached enamel are less proteins, lipids and nucleic acids have a number of
numerous, less well defined and shorter than those potential pathological consequences (38). To prevent
in unbleached enamel (100). Bonding to dentine these potential dangers, the body has a number of
may be altered after bleaching (33) and the smear defense mechanisms at the tissue and cellular level
layer may be removed (61). Bonding between glass that work to repair any damage sustained. Enzymes
ionomer and dentine may also be affected by the such as catalase, peroxidase and superoxide dimu-
possible precipitation of hydrogen peroxide and tase are commonly found in body fluids, tissues and
collagen that forms on the cut dentine surface after organs to metabolize hydrogen peroxide (37, 57).
tooth bleaching (100). Salivary peroxidase has been suggested to be the
The residual oxygen in the tooth surface also bodyÕs most important and effective defence against
inhibits the polymerization of the composite resin potential adverse effects (19). The hydrogen peroxide
and disrupts the surface (62, 93). However, bond exposure dose has been estimated to be approxi-
strength improves if the procedure is delayed for 2 mately 3.5 mg for a treatment of both arches using
weeks post-bleaching. 10% carbamide peroxide (77), while the oral cavity is
capable of decomposing more than 29 mg of hydro-
gen peroxide per minute (84).
Effects on restorative materials The dermal toxicity of hydrogen peroxide is low,
with concentrations of up to 35% not considered as
The effects of bleaching agents on composite resins being irritant to rabbit skin; however, concentrations
are conflicting, ranging from no effect (7, 67, 83) to of greater than 50% are corrosive. Various mouth
alteration of surface hardness (5, 42), surface rough- rinses and oral antiseptics (10 and 15% carbamide
ening ⁄ etching (127) and changes in tensile strength peroxide, and hydrogen peroxide up to a concentra-
(31). However, these effects were very small and tion of 3%) have been used for some time with no
considered unlikely to be clinically significant (140). detectable ill effect on humans and have been ap-
Prolonged bleaching treatment may cause micro- proved by the US Food and Drug Administration
structural changes in amalgam surfaces and this may since 1979. On the contrary, reports are of beneficial
increase exposure to the patient of toxic by-products effects on gingival irritation and plaque accumula-
(115). Existing amalgams may change in color from tion, and an anticariogenic action (124).
black to silver, but not all combinations of amalgam Hydrogen peroxide has been found not to be car-
and bleaching agents result in higher mercury levels. cinogenic, mutagenic or teratogenic (37, 78, 159), and
Little effect is reported on gold or porcelain resto- concerns of toxicity or serious damage to soft tissues
rations; however, the glass ionomer matrix may show appear to be unfounded (49). Initially, concerns were
alteration in its matrix (63). Provisional crowns made raised about the role of hydrogen peroxide in muta-
of methyl methacrylate may discolor to become genesis on the basis of some in vitro tests that were
orange, but other materials are not affected (111). not reproduced in vivo (67). In fact, the frequency of
genetic mutation induced by 10% carbamide perox-
ide is not significantly different from that of a phys-
Toxic effects iological saline control (159). The only side effect
reported from ingesting large quantities of a car-
Carbamide peroxide administered as a home bamide peroxide home bleaching product was a
bleaching agent breaks down to produce hydrogen laxative effect from the presence of glycerine found
peroxide and urea in the mouth. The toxicology of within the gel (3).
hydrogen peroxide has been reviewed by the Euro-
pean Centre for Ecotoxicology and Toxicology of
Chemicals (36), and others (77), who reported that Evidence of efficacy of
hydrogen peroxide is found to occur naturally in tooth-whitening techniques
many vegetables and is produced in humans during
normal metabolism of aerobic cells. In addition to A variety of case reports and small clinical studies
this, phagocytic cells, such as neutrophils and mac- have shown that a 10% carbamide peroxide gel used
rophages, provide an important source of endoge- in night guard vital bleaching techniques produces
nous hydrogen peroxide and play an essential role in predictable results (66, 69, 74, 75, 85, 88, 104, 109,
defence against various pathological microorganisms 116) as do hydrogen peroxide strips (44). Similarly,
(148). However, free radical oxidative reactions with Ôpower bleachingÕ using 35% hydrogen peroxide, with

157
Sulieman

or without light and ⁄ or heat activation, has also been resulted in heat or light that catalysed breakdown of
shown to be effective (60, 130, 131, 133). the gels. They also concluded that proprietary
Heyman et al. (59) reported a mean change of 7 chemicals added to the gels caused them to perform
units on the Vita shade guide after bleaching with a differently from the 35% aqueous hydrogen peroxide
10% carbamide peroxide gel over 7 days. However, liquid controls used in the laboratory tests. Further-
there was a wide range of responses, ranging from 3 more, these chemicals were also probably responsi-
to 13 units, which highlights the unpredictable nature ble for the reduced time required to bleach with the
of teeth. Papathanasiou et al. (104) reported a mean Xe-halogen light. Contrary to these results, Luk et al.
change of 8 Vita units when using a 15% in-office (81) reported that color and temperature changes
hydrogen peroxide system, whereas Gerlach & Zhou were significantly affected by an interaction of the
(44) reported a mean change of 5.5 units when using bleach and light variables. The application of lights
a whitening strip, but 25% of their sample had a significantly improved the whitening efficacy of some
shade change in excess of 8 units. bleaching materials but it caused a significant tem-
Clinical and laboratory studies have also reported perature increase in the outer and inner tooth sur-
tooth-whitening changes using the L*a*b* system of faces. Other workers have also reported a study on
measurement (25). For example, an in vitro study on the use of lights for in-surgery bleaching and con-
dentine by White et al. (156) reported an improve- cluded that the use of lights with the peroxide gel
ment of DL* of 7 units when a 10.5% carbamide significantly lightened teeth more than peroxide or
peroxide gel was used for 30 h. Similarly, Gerlach & light treatment alone (143). The results of this study
Zhou (44) reported an improvement of DL* of 2 units must be interpreted with caution as the reported
with a whitening strip product. shade improvement with light-only application was
Various workers have compared two or more night 4.9 shade guide units, which was probably the result
guard vital bleaching agents clinically; very similar of a great deal of tooth dehydration. In another
results were obtained, usually in the magnitude of in vitro study, it was found that an activating light
about 7 shade guide units improvement (82). Ro- source did improve the whitening effect but the
senstiel et al. (112) reported on a single power freshness of the hydrogen peroxide was probably
bleaching session in a group of 20 young adults, more of a contributing factor (135).
which produced an average whitening effect of 6.2 L* Researchers at Procter & Gamble have reported on
units (as measured using a colorimeter) that was still many trials using a whitening strip and various con-
detectable 6 months post-treatment. In-surgery centrations of carbamide peroxide (44). In general,
bleaching has been compared with night guard vital the magnitude of the whitening response decreased
bleaching using 10% carbamide peroxide in a 3- with age and, on average, for every 10 years of aging,
month single blinded clinical study (163). Compari- individuals should expect approximately 0.3 units
sons were made of the color change, color relapse as less whitening benefit. Baseline color also affected
well as tooth and gum sensitivity. A 14-day home the response, with the greatest average whitening
treatment was compared with 60 min of in-surgery seen in individuals with more yellow teeth. For both
bleaching consisting of two clinical bleaching ses- strip and tray systems used, increasing the peroxide
sions of three 10-min applications. The at-home concentration was observed to improve the whiten-
bleaching produced significantly lighter teeth, but ing response (47, 48, 141). When treatment time was
significantly higher cervical sensitivity. Colour doubled to 28 days using these whitening strips, an
relapse for both bleaching techniques stabilized by 6 additional 29% whitening effect was achieved com-
weeks. pared with the normal treatment duration of 14 days
Long-term results of bleaching efficacy were re- (34, 50). Pre-brushing teeth prior to the application of
ported by Leonard (72), with at least 43% shade whitening strips was also found to yield a signifi-
retention without retreatment at 10 years. cantly more efficacious whitening result (50), al-
The effect of the lights used for in-surgery bleach- though no explanation for this was offered.
ing techniques have been the subject of various de- After the introduction of a new higher-concentra-
bates as to their efficacy in improving the bleaching tion whitening strip (14% hydrogen peroxide), which
process (6, 70, 81). Hein et al. (56) reported that the was thinner and incorporated a smaller volume of
three lights used in their study (halogen curing light, bleaching gel, various comparative trials were re-
Xe-halogen light and metal halide light) did not ported in a pooled report (43). Efficacy results for
lighten teeth more than their bleach gels alone and these strips were significantly better than placebo or
concluded that output from any of the lights used pooled positive controls evaluated in clinical trials

158
An overview of tooth-bleaching techniques

assessing tooth shade. The reported irritation and dentine, which can be changed by bleaching tech-
patient tolerability were similar to those reported niques (121, ten Bosch and Coops, 1995). Some
with previous lower-concentration strips and other studies, using 35% hydrogen peroxide, have reported
marketed positive bleaching controls. color changes in both enamel and dentine (3, 52, 91,
Hydrogen peroxide (8.7%), carbamide peroxide 92, 98, 132). Others dispute the idea of color change
(18%) and sodium percarbonate (19%) paint-on- in dentine and believe that this occurs in enamel
bleaching agents have been introduced directly to the only, thereby masking the unchanged dentine (21).
public as over-the-counter preparations. The shade However, the successful bleaching of tetracycline-
improvements with these agents were reported to be stained teeth, and those with dentinogenesis imper-
about 4 shade guide units from baseline (41) with a fecta (30, 61), add weight to the argument that the
reduction in yellowness (Delta b*) of about )0.95 color change takes place primarily within dentine.
units (43). McCaslin et al. [1999] reported on a study using 10%
Long-term efficacy has been reported by Leonard carbamide peroxide and its effect on dentine color
(72), with shade retention without retreatment in at changes, and found that the color change in dentine
least 43% of subjects at 10 years post-treatment. The occurred at a uniform rate.
initial efficacy of the night guard vital bleaching A study by Carrillo et al. (20), of inside ⁄ outside
technique was 98% for nontetracycline-stained teeth, bleaching of nonvital teeth and the surrounding vital
and, with extended treatment times for tetracycline- teeth, reported an average Vita shade change of 15
stained teeth, 86% of these teeth were lightened. and 6 for the nonvital and vital teeth respectively.
Laboratory studies have reported on the efficacy of Friedman (39) also reported very favourable shade
different concentrations of carbamide peroxide. Al- changes for nonvital bleaching, but was cautious over
though higher concentrations of 10 and 16% long-term results (1–5 years) with 50% shade relapse
produced a quicker 2-shade shift than a 5% con- observed.
centration, the eventual result on whitening was the
same for all concentrations (75). Other studies that
compared various concentrations of carbamide per- Indications and contraindications
oxide and hydrogen peroxide also found that the for bleaching
eventual result was the same, but the time taken to
reach that end point was quicker with high concen- Nearly every patient can have their teeth bleached,
trations of bleaching agents (130, 136). In a similar but not every case is guaranteed to have a successful
clinical study on patients with tetracycline-stained outcome or be enough to satisfy the esthetic needs of
teeth, more rapid bleaching effects were achieved the patient. The indications for bleaching are basi-
with a higher concentration of carbamide peroxide cally the same for both in-surgery and home
(15 and 20%) but the end results were the same as bleaching but the clinician must decide which
those for a lower concentration of carbamide perox- method is best suited to the patientÕs needs.
ide (10%) (87). In a separate study comparing the
clinical effect of 10 and 15% carbamide peroxide
Indications
using three different shade-assessment methods, re-
sults at 2 weeks showed a significantly better shade • generalized staining.
improvement for the higher-concentration product. • ageing.
However, by 6 weeks there were no statistical signif- • smoking and dietary stains such as those of tea and
icant differences between the two concentrations coffee.
(86). • fluorosis.
To establish the efficacy of both 20% carbamide • tetracycline staining.
peroxide and the equivalent concentration of 7.5% • traumatic pulpal changes.
hydrogen peroxide used in an in vivo study of day- • pre-restorative and post-restorative treatments.
time use of bleaching agents, it was found that there Very severe tetracycline staining may not be amena-
were no significant differences between the two ble to bleaching alone and therefore combination
products in terms of tooth lightness, and gingival and treatments, such as bleaching and veneers, may be
tooth sensitivities (95). considered. Prior bleaching reduces the amount of
The mechanism of tooth color change during tooth substance removed in preparation for the ve-
bleaching is poorly understood. Many workers sug- neers, which would otherwise have been necessary in
gest that tooth color is primarily determined by the order to mask the stain and allow for porcelain build

159
Sulieman

up. Fluorosis with multiple spots of varying colors The sensitive patient can have fluoride-desensitizing
may require a combination of bleaching and micro- gels applied to teeth in the bleaching trays for a
abrasion using hydrochloric acid and abra- period of a few weeks prior to bleaching. Elderly pa-
sives ⁄ polishes (29). Bleaching is also indicated prior tients with yellow receded roots present a problem in
to extensive restorative cosmetic work in the anterior that the roots do not bleach as readily compared with
region of the mouth in order to allow general the crowns, leaving an obvious mismatch that re-
improvement of the shade of the teeth, which are quires to be corrected by restorative dentistry. If the
then matched with the new restorative restorations. patients are aware of this and are willing to undergo
Bleaching can also be used post-restoratively when restorative work to address this issue, then it cannot
patients present with incorrectly made restorations be considered as a contraindication.
whose shades are lighter than the natural dentition.
As mentioned above, bleaching can be undertaken
in most cases but some contraindications are worthy Who best to bleach?
of mention. Patients with high expectations may
never be satisfied and should be identified by asking a Although it is difficult to predict the result of
simple question as to what they hope to achieve with bleaching teeth for every individual, there are some
the bleaching procedure. Patients who reply Ôdazzling guidelines gained from various studies, reports and
whiteÕ or words to that effect should be treated personal experience. For instance, the effect of
cautiously, while more reasonable replies may be Ôa bleaching in older patients who have teeth with small
freshening look to the teethÕ or a Ôlittle lighterÕ. Decay, pulps and various accumulated dietary stains, as well
peri-apical lesions and sensitivity does not preclude as the aging discoloration caused by secondary den-
those patients from bleaching, but these conditions tine deposition, is relatively predictable. In the au-
have to be resolved prior to bleaching. thorsÕ experience, teenagers with yellow teeth or with
basically white teeth except for the yellow canines
tend to respond well to bleaching. Browns stains are
Contraindications
more difficult to bleach but generally respond to
• patientsÕ high expectations. longer bleaching regimens than stains caused by
• decay and peri-apical lesions. nicotine (51). White fluorosis spots tend not to bleach
• pregnancy. but will become less obvious as a result of the light-
• sensitivity, cracks and exposed dentine. ening of the surrounding tooth area (51).
• existing crowns or large restorations in the smile Severe tetracycline staining may be very difficult to
zone. bleach but mild-to-moderate tetracycline staining
• elderly patients with visible recession and yellow tends to respond to extended bleaching regimes of 3
roots. to 6 months (51). Different brands of tetracycline
Existing crowns or restorations that need to be present with different colored tooth banding, which
changed following bleaching may be considered as a is especially difficult to treat as not all respond well to
contraindication for patients who do not want or bleaching, leaving the possible need to use restora-
cannot afford this extra financial burden. It is not tions to cover the nonresponsive band (51). Figure 3
always necessary to change composites following shows an example of fluorosis brown stain removed
bleaching because some types of composites display using 10% carbamide peroxide.
a chameleon effect, taking on the shade of the sur-
rounding tooth and blending in well, if not quite
Bleaching protocol
perfectly. The other contraindications mentioned
above can be rectified before embarking on a Diagnosis of the cause of the discoloration should be
bleaching course of treatment. For instance, in the made and recorded in the patientÕs notes. The op-
case of decay, a restoration can be preformed and tions for treatment can be extrinsic stain removal,
resurfaced for the correct bleached shade about 2 bleaching or both. Other options, such as veneers and
weeks post-bleaching once the end shade has stabi- crowns, should also be discussed with the patient and
lized and to allow for the dissipation of the residual recorded in the notes.
oxygen that may inhibit the composite bond to The teeth that are to be bleached should be iden-
enamel ⁄ dentine. Similarly, apical lesions should be tified and checked for the following:
treated and the root canal filling sealed effectively • vitality.
using a glass ionomer material prior to bleaching. • caries.

160
An overview of tooth-bleaching techniques

pre-operative photograph with the shade tab in situ


should always be taken under standardized lighting
conditions without using the dental operating light,
which would result in washout of the shade. After all
the relevant explanations, options, limitations and
prognosis have been discussed with the patient, a
consent form should be signed and the patient
referred for a hygiene session about 7–10 days prior
to the bleaching procedure.

Home bleaching
Bleaching material ⁄ regimen
Nearly all the bleaching materials on the market have
been shown to work to a comparable extent (82).
Generally, the higher-concentration, thicker, more
viscous materials produce a lightening effect more
quickly than lower-concentration, less viscous
materials. However, higher concentrations tend to
produce more cases of thermal sensitivity (107).
The choice of material to use depends on a number
Fig. 3. The use of 10% carbamide peroxide to remove a of factors, including the type of discoloration present
brown flourotic stain from a maxillary right central and how dark the teeth are initially. However, the
incisor. most important consideration has to be the patient,
their lifestyle, the time available for bleaching
and whether there are existing problems with tooth
• cracks.
sensitivity.
• recession, exposed dentine.
The bleaching regimen is therefore determined by
• developmental defects such as white spots.
the patientsÕ lifestyle, preference and schedule. If the
In addition, the presence of composite fillings, ve-
patient is happy and able to wear trays overnight,
neers, crowns or highly translucent teeth should be
then 10% carbamide peroxide worn for 8 h overnight
noted. Patients must be warned that these will not
is the treatment of choice (Fig. 4). However, if time is
change shade but their margins may merely be
at a premium, this regimen is not recommended as
cleaned up by the bleaching agent acting on the
bleaching will take about 4 weeks in total as the top
surrounding tooth structure. Hence, they may need
and the bottom teeth are bleached separately. In the
replacement following the bleaching treatment.
authorsÕ experience, some patients are able to wear
Highly translucent teeth do not bleach well and
both upper and lower trays simultaneously overnight,
sometimes appear greyer rather than whiter (45).
Patients need to be aware of all these points and the
information again needs to be recorded in the notes.
Some authors advocate the use of full-mouth peri-
apical radiographs to document the size and vitality
of pulps to predict sensitivity levels or check for peri-
apical pathology (51). In view of the current ioniza-
tion radiation regulations and the unnecessary
exposure of the patient to high levels of radiation,
other forms of vitality testing, such as ethyl chloride
or electric pulp testers, are advised instead. Any teeth
that require root canal therapy should have this car-
ried out prior to the bleaching procedure. Following
the assessment of the teeth, the shade should be Fig. 4. Loaded tray inserted into the patients mouth before
agreed with the patient and recorded in the notes. A removal of excess bleaching agent.

161
Sulieman

thereby reducing the bleaching period to 2 weeks, but ucts; they are aimed at reducing the concentration
many patients cannot cope with this regimen. Higher and amount of bleaching gel used, or the bleaching
concentrations of carbamide peroxide, such as 15 or time. The trays are trimmed back, if necessary, and
20%, can be selectively used to treat darker teeth less gel is used in the trays with the excess thoroughly
within an arch such as canines while still using 10% removed. The patients can be instructed to apply the
carbamide peroxide to bleach the lighter teeth within bleaching materials only on alternate nights, or even
the arch at the same time. every third night, to reduce the problems of sensi-
Some patients are unable to wear trays overnight tivity. This can delay the treatment time but ensures
and prefer daily use, which has the advantage of more that the patient is comfortable with the bleaching
frequent replenishment of the bleaching gel for regime.
maximum bleaching effect, but both occlusal pressure
and increased salivary flow may dilute the gel (35).
Nonvital bleaching techniques
Home bleaching side effects
There are a number of nonvital bleaching techniques
Some patients experience problems with gingival or available, which include Ôwalking bleach and modi-
soft tissue irritation during home bleaching, but the fied walking bleachÕ, nonvital power bleaching, also
vast majority of problems are those of tooth sensi- known as Ôthermo ⁄ photo bleachingÕ, and Ôinside ⁄
tivity, which have been reported to affect about two- outside bleachingÕ.
thirds of patients (61, 99). Painful gums may be the
result of incorrectly fitting trays impinging on them
Walking bleach technique
or the use of excess material in the trays. The trays
can be easily trimmed back and polished, while the First described by Spasser (128), the walking bleach
patient can be instructed to use less material if other technique involved sealing into the tooth a mixture of
areas of mucosa or soft tissues are irritated. Some sodium perborate with water by introducing it into
patients who bleach teeth overnight report a metallic the pulp chamber. After 1 week the patient would
taste sensation immediately following tray removal, return and the procedure would be repeated until the
but this usually disappears after about 2 h (42). desired whitening had occurred. The technique was
Thermal tooth sensitivity is a common side effect modified using a combination of 30% hydrogen
noticed by patients as early as the third day of peroxide and sodium perborate sealed into the pulp
bleaching following the removal of trays and may chamber for 1 week Ômodified or combination walk-
persist for 3–4 h afterwards. Patients who experience ing bleach techniqueÕ (102, 103). Sodium perborate is
severe sensitivity should be advised to stop bleaching stable when in the form of a dry powder, but in the
and the sensitivity should be treated. Treatment can presence of acid, warm air or water it decomposes to
take the form of fluoride-containing toothpastes or form metaborate, hydrogen peroxide and nascent
neutral sodium fluoride gels in the bleaching trays oxygen. Hydrogen peroxide mixed with sodium per-
worn overnight. Desensitizing potassium nitrate, or borate potentiates its effect and produces a better
potassium nitrate and fluoride-containing gels, are bleaching effect (114).
also available for use in trays for about 2 h before or Prior to any bleaching procedure the nonvital tooth
after the bleaching procedure. Potassium nitrate in must be radiographed to assess the quality of the root
toothpastes takes about 3 weeks to reduce sensitivity canal obturation and the apical tissues. Any defi-
measurably, but when put in a tray for 10–30 min, ciencies must be rectified before bleaching.
relief is almost immediate. Lower degrees of sensitivity The Ôcombination bleach techniqueÕ differs from
can be treated with desensitizing toothpaste rubbed or the above only in that sodium perobrate is mixed
brushed onto the cervical necks of the affected teeth. with 30% hydrogen peroxide (or lower concentra-
Fluoride acts primarily as a blocker of dentinal tions), instead of water, to form a thick paste that is
tubules, which acts to slow down the dentinal fluid sealed into the cavity. The procedure is quicker acting
flow that causes sensitivity, while potassium nitrate and hence can produce results after 1 week. The
acts like an anesthetic by preventing the nerve from current walking bleach technique involves sealing in
repolarizing after it has depolarized in the pain cycle 10% carbamide peroxide instead of sodium perbo-
(51). rate without needing to mix the product, simply
Other forms of treating sensitivity are passive in syringing the gel into the cavity and reviewing the
terms of not involving specific desensitizing prod- patient in 3 days.

162
An overview of tooth-bleaching techniques

Internal nonvital power bleaching


This technique is the least favoured because of its use
of high temperatures and the probable increased risk
of internal resorption. Hydrogen peroxide gel at a
concentration of 30–35% is applied into the pulp
chamber and activated either by light or heat. The
temperature is usually between 50 and 60 C and
maintained for 5 min before the tooth is allowed to
cool down for a further 5 min before the gel is re-
moved by washing with water for a further minute
(114). The tooth is dried and the Ôwalking bleach
techniqueÕ is used between visits until the tooth is
reviewed 2 weeks later to assess if further treatment is
necessary.
A variation of this technique uses 35% hydrogen
peroxide gel applied both internally to the pulp
chamber and externally to the labial surface of the
tooth, with light activation internally and externally.
High temperatures are not involved and the same
preparation protection techniques are used on the
tooth. Light activation both internally and externally
can be in the form of a conventional halogen-curing
light, plasma arc lamp or a diode laser. Following this Fig. 5. Bleaching of a nonvital upper left central incisor
procedure, the tooth is washed and dried before being using the inside ⁄ outside technique.
sealed with a temporary restoration. The patient is
reviewed 2 weeks later when the shade would have manual dexterity to place the bleaching agent into
stabilized and the tooth is ready for a definitive res- the cavity. Coupled to the ease with which overuse
toration to be placed or is bleached further if required. can lead to overbleaching the tooth, and with the
potential for external resorption still existing, al-
though reduced, this technique is by no means
Inside ⁄ outside bleaching
without its risks.
This technique is a combination of internal bleaching As with the modified bleaching technique, the in-
of nonvital teeth using the home bleaching tech- side ⁄ outside bleaching technique has been modified
nique. The preparation of the nonvital tooth is exactly by use of varying concentrations of carbamide per-
the same as for the Ôwalking bleach techniqueÕ in that oxide, such as 5, 16, 22 or 35%, as used in the waiting
a protective barrier is placed over the root canal room technique. Figure 5 shows a typical example of
system using glass ionomer material and the access the results achieved using this technique.
cavity is completely cleaned in readiness for the
bleaching procedure.
The advantage of this technique for bleaching Power bleaching
nonvital teeth is that it utilizes both an internal and
an external approach for the bleaching agent. The use The power bleaching technique is used on those
of a lower concentration of bleach, usually 10% car- patients who do not have the necessary time avail-
bamide peroxide, is thought to reduce the risk of able for home bleaching, who have a problem with
external resorption. There is no need for frequent wearing trays that may cause them to gag or who
changes in temporary dressings, as experienced with even find the taste of the home bleaching gel not to
the walking bleach when the oxygen build up within their liking. Another advantage is that the immediate
the pulp chamber dislodged the dressing. Addition- results produced in power bleaching can be used to
ally, the technique achieves the lightening effects motivate the patient to continue with home bleach-
within a matter of days compared with weeks. ing top-up treatment. It must be emphasized that
The main disadvantages of this technique are the although there is an immediate result with power
need for patient compliance and a little degree of bleaching, it is by no means necessarily the end point

163
Sulieman

in terms of tooth whiteness and further bleaching low the critical temperature once the power output
sessions may be necessary. It can be likened to the was reduced from 3 to 2 W (137).
home bleaching procedure that produces results There are many different materials available, but
within the first 4 days for most people but over the broadly speaking they are either based on 35% car-
next couple of weeks this is further enhanced until it bamide peroxide or hydrogen peroxide of the same or
reaches a terminal end point where the tooth shade higher concentration. Hydrogen peroxide is more
does not improve any further. widely used as the power bleaching agent, but the
The increased surgery time required for in-surgery range of concentrations in current use varies from
bleaching is obviously a disadvantage, as it makes the about 17–50% and the bleaching time for which they
procedure more expensive for the patient. Some re- are used also varies. Thirty-five per cent carbamide
ports also highlight that power bleaching causes peroxide yields approximately 10% hydrogen perox-
dehydration of the teeth, thereby giving a falsely ide and is used in certain bleaching systems, some-
lighter shade immediately post-treatment (6). This times known as Ôwaiting room bleachÕ, because the
causes further problems, with patients perceiving patient wears the custom-made trays full of the
that there is color regression or rebound following material and waits in the waiting room of the surgery.
rehydration of the teeth. Some manufacturers have Thirty-five per cent hydrogen peroxide is available
addressed this problem by producing gels that con- in a powder–liquid combination mixed together to
tain 10–20% water, which rehydrates the teeth produce a gel, or in a ready-made gel to which liquid
throughout the bleaching procedure, while others is added. There are many different combinations
have tackled the problem by using lower concentra- available depending on the system or activation
tions of hydrogen peroxide (15%), which is a water- method used.
based solution, thereby increasing the water content
by 20%. However, by far the biggest disadvantage of
the power bleaching procedure is the caustic nature Light activation
of the 35–50% hydrogen peroxide used. The need for
a meticulous protocol in handling, applying, removal Various types of curing lights are used to activate the
and disposal of these materials is essential. The risk bleaching gel or expedite the whitening effect. Ini-
of tissue burns to the lips, cheeks, gingiva, the rest of tially, conventional curing lights were used but these
the face or eyes makes isolation and protection were quickly joined by lasers and plasma arc lamps.
techniques mandatory (Fig. 6). In addition, some systems are activated by a chemi-
The main safety issue concerning the activating cal reaction upon mixing two gels, while others utilize
lights used in power bleaching is heat generation and a dual-activation system.
its effect on the pulp. Recent research showed that Halogen curing lights can be used with a number of
the increase in the intrapulpal temperature with most different systems and generally activation is via the
bleaching lamps was below the critical threshold lightÕs bleach mode for 30 s per tooth and the appli-
of a 5.5 C increase thought to produce irreversible cation involves three 10-min passes. Plasma arc
damage. The only lamp that produced an intrapulpal lamps are also used in a similar way to halogen cur-
temperature increase above this threshold was the ing lights but, with the aid of a full smile illuminator,
laser-based lamp, and this was also found to be be- they can act in the same way as Xenonhalogen lights,
irradiating both arches at the same time, which is
generally three 10-min passes. Similarly, metal halide
lamps are used with a two-part 25% hydrogen per-
oxide gel in a dual-arch technique employing three
20-min passes followed by the application of sodium
fluoride gel.
Diode lasers of 830 and 980 nm wavelengths can be
used for tooth bleaching in combination with 35–
50% hydrogen peroxide gel. The gel is produced by
mixing the hydrogen peroxide liquid with a powder
containing mainly fumed silica and a blue dye. The
blue dye absorbs the laser wavelength and heats up
Fig. 6. Isolation of teeth and gums typically used in a to cause the controlled breakdown of the hydrogen
power bleaching procedure. peroxide to oxidizing perhydroxyl free radicals.

164
An overview of tooth-bleaching techniques

Waiting room bleach technique 8. Bentley CD, Leonard RH, Crawford JJ. Effect of whitening
agents containing carbamide peroxide on carcinogenic
bacteria. J Esthet Dent 2000: 12: 33–37.
Thirty-five per cent carbamide peroxide is activated 9. Bevenius J, Lindskog S, Hultenby K. The micromorphol-
by holding the syringe under hot running water for a ogy in vivo of the buccocervical region of premolar teeth
few minutes prior to use. The gel is transferred into in young adults. A replica study by scanning electron
the custom-made tray and the excess material re- microscopy. Acta Odontol Scand 1994: 52: 323–334.
10. van der Bijl P, Pitigoi-Aron G. Tetracyclines and calcified
moved from the patientsÕ mouth before asking the
tissues. Ann Dent 1995: 54: 69–72.
patient to sit in the waiting room for about 30–60 11. Bitter NC. A scanning electron microscopy study of the
min. After this time has elapsed the patient returns effect of bleaching agents on the enamel. A preliminary
and the gel is suctioned and rinsed off the teeth. The report. J Prosthet Dent 1990: 67: 852–855.
procedure can be repeated two or three times more 12. Bitter NC. A scanning electron microscopy study of the
long term effect of bleaching agents on the enamel sur-
in the one session.
face in vivo. Gen Dent 1998: 46: 84–88.
Power bleaching may frequently require more than 13. Bitter NC, Sanders JL. The effect of four bleaching agents
one visit to produce an optimal result. However, for on the enamel surface: a scanning electron microscopy
many patients a single visit is enough to satisfy their study. Quintessence Int 1993: 24: 817–824.
esthetic needs and no further treatment is required. 14. Bowles WH, Bokmeyer TJ. Staining of adult teeth by mi-
nocycline: binding of minocycline by specific proteins.
Power bleaching should be used in cases where time
J Esthet Restor Dent 1997: 9: 30–34.
is at a premium with patients requiring faster results 15. Bowles WH, Thompson LR. Vital bleaching: the effects of
and in cases where it is felt that the patient needs a heat and hydrogen peroxide on pulpal enzymes. J Endod
Ôkick startÕ before continuing with home bleaching. It 1986: 12: 108–112.
can also be used on teeth with different stain etiol- 16. Bowles WH, Ugwuneri Z. Pulp chamber penetration by
ogies, but must be carried out with meticulous care hydrogen peroxide following vital bleaching procedures.
J Endod 1987: 8: 375–377.
and attention as a result of the caustic nature of the
17. Burgmaier GM, Schulze IM, Attin T. Fluoride uptake and
35% hydrogen peroxide used. development of artificial erosions in bleached and fluo-
The goal of modern dentistry is maximum preser- ridated enamel in vitro. J Oral Rehabil 2002: 29: 799–804.
vation of tooth substance with excellent esthetics. 18. Cameron C, Widmer R. Handbook of Paediatric Dentistry,
Bleaching alone, or in combination with minimally 2nd edn. Philadelphia, USA: Mosby, 2003.
19. Carlsson J. Salivary peroxidase: an important part of our
invasive adhesive dentistry, very often fulfils this goal
defence against oxygen toxicity. J Oral Pathol 1987: 16:
without the need to progress to the much more 412–416.
destructive techniques of veneers, crowns and 20. Carrillo A, Arredondo Trevino MV, Haywood VB. Simul-
bridges. taneous bleaching of vital teeth and an open-chamber
nonvital tooth with 10% carbamide peroxide. Quintes-
sence Int 1998: 29: 643–648.
21. Chiappinelli JA, Walton RE. Tooth discolouration resulting
References from long-term tetracycline therapy: a case report.
Quintessence Int 1992: 23: 539–541.
1. Addy A, Moran J, Newcombe R, Warren P. The compar- 22. Christensen G. Why resin curing lights do not increase
ative tea staining potential of phenolic, chlorhexidine and tooth lightening. Status report. CRA Newsletter 2000: 24: 6.
anti-adhesive mouthrinses. J Clin Periodontol 1995: 22: 23. Cohen SC. Human pulpal response to bleaching proce-
923–928. dure on vital teeth. J Endod 1979: 5: 134.
2. Addy M, Prayitno S, Taylor L, Cadogan S. An in vitro study 24. Cohen S, Parkins FM. Bleaching tetracycline stained vital
of the role of dietary factors in the aetiology of tooth teeth. Oral Surg Oral Med Oral Pathol 1970: 29: 465–471.
staining associated with the use of chlorhexidine. J Peri- 25. Commission Internationale de lÕEclairage. The L*a*b*
odontal Res 1979: 14: 403–410. system. Austria: Wien, 1976.
3. Albers HF. Home bleaching. ADEPT Report 1991: 2: 9. 26. Cooper J, Bokmeyer TJ, Bowles WH. Penetration of the
4. Baik JW, Rueggeberg FA, Liewehr FR. Effect of light en- pulp chamber by carbamide peroxide bleaching agents.
hanced bleaching on in-vitro surface and intrapulpal J Endod 1992: 18: 315–317.
temperature rise. J Esthet Restor Dent 2001: 13: 370–378. 27. Cotton FA, Wilkinson G. Oxygen. In: Cotton FA, Wilkinson
5. Bailey SJ, Swift EJ. Effects of home bleaching products on G, editors. Advances in inorganic chemistry. A compre-
resin. J Dent Res 1991: 70: 570. (Abstract No. 2434). hensive text. New York: Interscience Publisher, 1972: 403–
6. Barghi NB. Making a clinical decision for vital tooth 420.
bleaching: at-home or in-office? Compend Contin Educ 28. Covington J, Friend G, Lamoreaux W. Carbamide peroxide
Dent 1998: 19: 831–838. tooth bleaching effects on enamel composition and
7. Baughan L, Dishman M, Covey DA. Effect of carbamide topography. J Dent Res 1990: 69: 175 (Abstract No. 530).
peroxide on composite bond strength. J Dent Res 1992: 71: 29. Croll TP. Enamel microabrasion for removal of superficial
281 (Abstract No. 1403). discolouration. J Esthet Dent 1989: 1: 14–20.

165
Sulieman

30. Croll TP, Sasa IS. Carbamide peroxide bleaching of teeth vital bleaching technique. Quintessence Int 1992: 27: 471–
with dentinogenesis imperfecta discolouration: report of a 488.
case. Quintessence Int 1995: 26: 683–686. 51. Haywood VB. A comparison of at-home and in-office
31. Cullen DR, Nelson JA, Sandvrik JL. Effect of peroxide bleaching. Dent Today 2000: 19: 44–53.
bleaches on tensile strength of composite resin material. 52. Haywood VB, Drake M. Research on whitening teeth
J Dent Res 1992: 71: 281 (Abstract No. 1405). makes news. NC Dental Review 1990: 7: 9.
32. Dahl JE, Pallesen U. Tooth bleaching – a critical review of 53. Haywood VB, Heymann HO. Nightguard vital bleaching.
the biological aspects. Crit Rev Oral Biol Med 2003: 14: Quintessence Int 1989: 20: 173–176.
292–304. 54. Haywood VB, Houck V, Heymann HO. Nightguard vital
33. Della Bona A, Barghi N, Berry TG, Godwin JM. In-vitro bleaching: effects of varying pH solutions on enamel
bond strength testing of bleached dentine. J Dent Res surface texture and colour change. Quintessence Int 1991:
1992: 71: 659 (Abstract No. 1154). 22: 775–782.
34. Donly KJ, Gerlach RW, Segura A, Walters PA, Zhou X. Post- 55. Haywood VB, Leech T, Heymann HO, Crumpler D,
orthodontic tooth whitening. J Dent Res 2001: 80: 151 Bruggers K. Nightguard vital bleaching: effects on enamel
(Abstract No. 924). surface texture and diffusion. Quintessence Int 1990: 21:
35. Dunn JR. Dentist-prescribed home bleaching: current 801–806.
status. Compend Contin Educ Dent 1998: 19: 760–764. 56. Hein DK, Ploeger BJ, Hartup JK, Wagstaff RS, Palmer TM,
36. ECETOC. Joint Assessment of Commodity Chemicals No. Hansen LD. In-office vital tooth bleaching: what do lights
22: Hydrogen Peroxide [CAS No. 7722-84-1]. Brussels, add? Compend Contin Educ Dent 2003: 24: 340–352.
Belgium: European Centre for Ecotoxicology and Toxi- 57. Heithersay GS. Invasive cervical resorption: an analysis of
cology of Chemicals, 1983. potential predisposing factors. Quintessence Int 1999: 30:
37. Fayle SA, Pollard MA. Congenital erythropietic porphyria- 83–95.
oral manifestations and dental treatment in childhood: a 58. Heithersay GS, Dahlstrom SW, Marin PD. Incidence of
case report. Quintessence Int 1994: 25: 551–554. invasive cervical resorption in bleached root-filled teeth.
38. Floyd RA, Schneider JE. Hydroxyl free radical damage to Aust Dent J 1994: 39: 82–87.
DNA. In: Vigo-Pelfrey C, editor. Membrane lipid oxida- 59. Heymann HO, Swift EJ, Bayne SC, May KN, Wilder AD,
tion. Boca Raton, FL: C.R.C. Press, 1990: 230–238. Mann GB, Peterson CA. Clinical evalusation of two
39. Friedman S. Internal bleaching: long term outcomes and carbamide peroxide tooth whitening agents. Compend
complications. J Am Dent Assoc 1997: 4: 51S–55S. Contin Educ Dent 1998: 19: 359–362.
40. Fugaro JO, Nordahl I, Fugaro OJ, Matis BA, Mjor IA. Pulp 60. Howard J. Patient-applied tooth whiteners. J Am Dent
reaction to vital bleaching. Oper Dent 2004: 29: 363–368. Assoc 1992: 132: 57–60.
41. Gambarini G, Testarelli L, De Luca M, Dolci G. Efficacy 61. Hunsaker KJ, Christensen GJ, Christensen RP. Tooth
and safety assessment of a new liquid tooth whitening gel bleaching chemicals-influence on teeth and restorations.
containing 5.9% hydrogen peroxide. Am J Dent 2004: 17: J Dent Res 1990: 69: 303.
75–79. 62. Jay AT. Tooth whitening: the financial rewards. Dent
42. Garber DA. Dentist monitored bleaching: a discussion of Manage 1990: 30: 28–31.
combination and laser bleaching. J Am Dent Assoc 1997: 63. Jefferson KL, Zena RB, Giammara BT. The effect of car-
128: 26–30. bamide peroxide on dental luting agents. J Dent Res 1991:
43. Gerlach RW, Barker ML. Professional vital bleaching using 70: 571 (Abstract No. 2440).
a thin and concentrated peroxide gel on whitening strips: 64. Jordan RE, Boksman L. Conservative vital bleaching
an integrated clinical summary. J Contemp Dent Pract treatment of discoloured dentition. Compend Contin Educ
2004: 5: 1–17. Dent 1984: 10: 803–807.
44. Gerlach RW, Zhou X. Vital bleaching with whitening 65. Jorgensen MG, Carroll WB. Incidence of tooth sensitivity
strips: summary of clinical research on effectiveness and after home whitening treatment. J Am Dent Assoc 2002:
tolerability. J Contemp Dent Pract 2001: 2: 1–15. 133: 1076–1082.
45. Goldstein RE. In-office bleaching: where we came from, 66. Kalili T, Caputo AA, Mito R, Sperbeck G, Matyas J. In vitro
where we are today. J Am Dent Assoc 1997: 128: 11S–15S. toothbrush abrasion and bond strength of bleaching en-
46. Gonzalez-Ochoa J. Histological changes to dental pulp amel. J Dent Res 1991: 70: 546 (Abstract No. 2243).
after vital bleaching with 10% carbamide peroxide (dis- 67. Kawachi T, Yahagi T, Kada T, Tazima Y, Ishidate M, Sasaki
sertation). Indianapolis: Indiana University School of M, Sugiyama T. Cooperative programme on short-term
Dentistry, 2002. assays for carcinogenicity in Japan. IARC Sci Publ 1980:
47. Gorlin RJ, Goldman HM Environmental pathology of the 27: 323–330.
teeth. In: Thoma KH, editor. ThomaÕs oral pathology, 6th 68. Kihn PW, Barnes DM, Romberg E, Peterson K. A clinical
edn. Vol. I. St Louis, USA: CV Mosby Co, 1971: 184–192. evaluation of 10 percent vs. 15 percent carbamide per-
48. Grobler SR, Senekal PJC, Laubscher JA. In vitro deminer- oxide tooth-whitening agents. J Am Dent Assoc 2000: 131:
alization of enamel by orange juice, apple juice, Pepsi 1478–1484.
Cola and Diet Pepsi Cola. Clin Prev Dent 1990: 12: 5–9. 69. Kowitz GM, Nathoo SA, Rustogi KN, Chemielewski MB,
49. Hamon CB, Klebanoff SJ. A peroxide mediated strepto- Wong R. Clinical comparison of Colgate Platinum Tooth
coccus mitis dependent antimicrobial system. J Exp Med Whitening system and Rembrandt Gel Plus. Compend
1973: 137: 438–450. Contin Educ Dent 1994: 17: S46–S51.
50. Haywood VB. History, safety and effectiveness of current 70. Kozak KM, Duschner HH, Gotz H, White DJ, Zoladz JR.
bleaching techniques and application of the night guard Effects of peroxide gels on enamel and dentin in vitro.

166
An overview of tooth-bleaching techniques

Research presented at the 30th Annual Meeting of the 92. McEvoy SA. Chemical agents for removing intrinsic stains
American Association for Dental Research, 2001. from vital teeth II. Current techniques and their clinical
71. Lai SC, Tay FR, Cheung GS, Wei SH. Reversal of com- application. Quintessence Int 1989: 20: 379–384.
promised bonding in bleached enamel. J Dent Res 2002: 93. McGukin RS, Thurmond BA, Osovitz S. In vitro enamel
81: 477–481. shear bond strengths following vital bleaching. J Dent Res
72. Leonard RH Jr. Long-term treatment results with night- 1991: 70: 377.
guard vital bleaching. Compend Contin Educ Dent 2003: 94. Moffitt JM, Cooley RO, Olsen NH, Hefferen JJ. Prediction
24: 364–374. of tetracycline induced tooth discolouration. J Am Dent
73. Leonard RH Jr, Garland GE, Eagle JC, Caplan DJ. Safety Assoc 1974: 88: 547–552.
issues when using a 16% carbamide peroxide whitening 95. Mokhlis GR, Matis BA, Cochran MA, Eckert GJ. A clinical
solution. J Esthet Restor Dent 2002: 14: 358–367. evaluation of carbamide peroxide and hydrogen peroxide
74. Leonard RH Jr, Haywood VB, Phillips C. Risk factors for whitening agents during daytime use. J Am Dent Assoc
developing tooth sensitivity and gingival irritation asso- 2000: 131: 1269–1277.
ciated with nightguard vital bleaching. Quintessence Int 96. Morely J. The esthetics of anterior tooth ageing. Curr Opin
1997: 28: 527–534. Cosmet Dent 1997: 4: 35–39.
75. Leonard RH, Sharma A, Haywood VB. Use of different 97. Murchison DF, Charlton DF, Moore BK. Carbamide per-
concentrations of carbamide peroxide for bleaching teeth: oxide bleaching: effects on enamel surface hardness and
an in-vitro study. Quintessence Int 1998: 29: 503–507. bonding. Oper Dent 1992: 17: 181–185.
76. Leonard RH Jr, Smith LR, Garland GE, Caplan DJ. 98. Nathanson D, Parra C. Bleaching vital teeth: a review and
Desensitizing agent efficacy during whitening in an at-risk clinical study. Compend Contin Educ Dent 1987: 8: 490–
population. J Esthet Restor Dent 2004: 16: 49–55. 497.
77. Li Y. Biological properties of peroxide-containing tooth 99. Nathonson D. Vital tooth bleaching: sensitivity and pulpal
whiteners. Food Chem Toxicol 1996: 34: 887–904. considerations. J Am Dent Assoc 1997: 128(Suppl.): 41S–
78. Li Y. Peroxide-containing tooth whiteners: an update on 44S.
safety. Compend Contin Educ Dent 2000: 28: S4–S9. 100. Nathoo SA, Chmielewski M, Kirkup RE. Effects of Colgate
79. Link J. Discolouration of teeth in alkaptonuria and par- Platinum Professional Toothwhitening System on mi-
kinsonism. Chronicle 1973: 36: 136. crohardness of enamel, dentin and composite resins.
80. Lopes GC, Bonissoni L, Baratieri LN, Vieira LC, Monteiro S Compend Contin Educ Dent 1994: 17: S627–S630.
Jr. Effect of bleaching agents on the hardness and mor- 101. Neumann LM, Christensen C, Cavanaugh C. Dental
phology of enamel. J Esthet Restor Dent 2002: 14: 24–30. eshetic satisfaction in adults. J Am Dent Assoc 1989: 118:
81. Luk K, Tam L, Hubert M. Effect of light energy on peroxide 565–570.
tooth bleaching. J Am Dent Assoc 2004: 135: 194–201. 102. Nutting EB, Poe GS. A new combination for bleaching
82. Lyons K, Ng B. Nightguard vital bleaching: a review and teeth. J South Calif Dent Assistants Assoc 1963: 31: 289.
clinical study. N Z Dent J 1998: 94: 100–105. 103. Nutting EB, Poe GS. Chemical bleaching of discoloured
83. Machida S, Anderson MH, Bales DJ. Effect of home endodontically treated teeth. Dent Clin North Am 1967:
bleaching agents on adhesion to tooth structure. J Dent Nov: 655–662.
Res 1992: 71: 600 (Abstract No. 678). 104. Papathanasiou A, Bardwell DS, Kugel G. A clinical study
84. Marshall MV, Gragg PP, Packman EW, Wright PB, Cancro evaluating a new chairside and take-home whitening
LP. Hydrogen peroxide decomposition in the oral cavity. system. Compend Contin Educ Dent 2001: 22: 289–294.
Am J Dent 2001: 14: 39–45. 105. Pearson D. The Chemical Analysis of Foods, 7th edn.
85. Matis BA, Cochran MA, Eckert G, Carlson TJ. The efficacy London, UK: Churchill Livingstone, 1976.
and safety of a 10% carbamide peroxide bleaching gel. 106. Potocnik I, Kosec L, Gaspersic D. Effect of 10% carbamide
Quintessence Int 1998: 29: 555–563. peroxide bleaching gel on enamel microhardness, micro-
86. Matis BA, Mousa HN, Cochran MA, Eckert GJ. Clinical structure and mineral content. J Endod 2000: 26: 203–206.
evaluation of bleaching agents of different concentra- 107. Pretty IA, Ellwood P, Aminian A. Vital tooth bleaching in
tions. Quintessence Int 2000: 31: 303–310. dental practice: 1. Professional bleaching. Dent Update
87. Matis BA, Yousef M, Cochran MA, Eckert GJ. Degradation 2006: 33: 288–304.
of bleaching gels in vivo as a function of tray design and 108. Price RB, Sedarous M, Hiltz GS. The pH of tooth-
carbamide peroxide concentration. Oper Dent 2002: 27: whitening products. J Can Dent Assoc 2000: 66: 421–426.
12–18. 109. Reinhardt JW, Eivins SC, Swift EJ. Clinical study of night-
88. McCaslin AJ, Haywood VB, Potter BJ, Dickinson GL, guard vital bleaching. Quintessence Int 1993: 24: 379–384.
Russell CM. Assessing dentin colour changes from night 110. Reyto R. Laser tooth whitening. Dent Clin North Am 1998:
guard vital bleaching. J Am Dent Assoc 1999: 130: 1485– 21: 755–762.
1490. 111. Robinson F, Haywood VB, Myers M. Effect of 10% car-
89. McCraken MS. Effects of vital bleaching on the hardness bamide peroxide on colour of provisional restoration
of enamel. Presented at the American Dental Association materials. J Am Dent Assoc 1997: 128: 727–731.
Student Table Clinic, Seattle, 1991. 112. Rosensteil SF, Gegauff AG, Johnston WM. Randomised
90. McCraken MS, Haywood VB. Demineralisation effects of clinical trial of the efficacy and safety of a home bleaching
10% carbamide peroxide. J Dent Res 1996: 24: 395–398. procedure. Quintessence Int 1996: 27: 413–424.
91. McEvoy SA. Chemical agents for removing intrinsic stains 113. Rotstein I. Bleaching non-vital teeth. In: Cohen S, Burns
from vital teeth I. Technique development. Quintessence RC. Pathways to the pulp. 7th edn. St Louis, USA: Mosby,
Int 1989: 20: 323–328. 1998: p. 674.

167
Sulieman

114. Rotstein I. Intra-coronal bleaching of non-vital teeth. In: 133. Sulieman M, Addy M, Rees JS. Development and evalua-
Greenwall L, editor. Bleaching techniques in restorative tion of a method in vitro to study the effectiveness of
dentistry. London: Martin Dunitz, 2001: 159–163. tooth bleaching. J Dent 2003: 31: 415–422.
115. Rotstein I, Mor C, Arwaz JR. Changes in surface levels of 134. Sulieman M, Addy M, Rees JS. Surface and intra-pulpal
mercury, silver, tin and copper of dental amalgams trea- temperature rises during tooth bleaching: a study in-vitro.
ted with carbamide peroxide and hydrogen peroxide Br Dent J 2005: 199: 37–40.
in vitro. Oral Surg Oral Med Oral Pathol Oral Radiol 135. Sulieman M, MacDonald E, Rees JS, Addy M. Comparison
Endod 1997: 83: 506–509. of three in-office bleaching systems based on 35%
116. Russell CM, Dickinson GL, Johnson MH. Dentist-super- hydrogen peroxide with different light activators. Am J
vised home bleaching with ten per cent carbamide Dent 2005: 18: 194–197.
peroxide gel: a six month study. J Esthet Dent 1996: 8: 136. Sulieman M, MacDonald E, Rees JS, Newcombe RG, Addy
177–182. M. Tooth bleaching by different concentrations of car-
117. Salman RA, Salman GD, Glickman RS, Super DG, Salman bamide peroxide and hydrogen peroxide whitening strips:
L. Minocycline induced pigmentation of the oral cavity. a study in vitro. J Esthet Restor Dent 2006: 93: 93–101.
J Oral Med 1985: 40: 154–157. 137. Sulieman M, Rees JS, Addy M. Surface and pulp chamber
118. Scherer W, Cooper H, Ziegler B, Vijayaraghavan TV. At temperature rises during tooth bleaching using a diode
home bleaching system: effects on enamel and cemen- laser: a study in vitro. Br Dent J 2006: 200: 631–634.
tum. J Esthet Dent 1991: 3: 54–56. 138. Sun G. The role of lasers in cosmetic dentistry. Dent Clin
119. Schulte JR, Morrissette DB, Gasior EJ, Czajewski MV. The North Am 2000: 44: 831–850.
effects of bleaching time on the dental pulp. J Am Dent 139. Sundell S, Koch G. Hereditary amelogenesis imperfecta:
Assoc 1994: 125: 1330–1335. epidemiology and classification in a Swedish child pop-
120. Sclare R. Hereditary opalescent dentine (dentinogenesis ulation. Swed Dent J 1985: 9: 157–169.
imperfecta). Br Dent J 1984: 84: 164–166. 140. Swift EJ. A method for bleaching discoloured vital teeth.
121. Seale NS, Thrash WJ. Systematic assessment of colour Quintessence Int 1988: 19: 607–611.
removal following vital bleaching of intrinsically stained 141. Swift EJ, Heymann HO, Ritter AV, Rosa BT, Wilder AD.
teeth. J Dent Res 1985: 64: 457–461. Clinical evaluation of a novel ÔtraylessÕ tooth whitening
122. Seghi RR, Denry I. Effects of external bleaching on system. J Dent Res 2001: 80: 151 (Abstract No. 921).
indentation and abrasion characteristics of human en- 142. Tam L. Clinical trail of three 10% carbamide peroxide
amel in vitro. J Dent Res 1992: 71: 1340–1344. bleaching products. J Can Dent Assoc 1999: 65: 201–205.
123. Shannon H, Spencer P, Gross K, Tira D. Characterisation 143. Tavares M, Stultz J, Newman M, Smith V, Kent R, Carpino
of enamel exposed to 10% carbamide peroxide bleaching E, Goodson JM. Light augments tooth whitening with
agents. Quintessence Int 1993: 24: 39–44. peroxide. J Am Dent Assoc 2003: 134: 167–175.
124. Shapiro WB, Kaslick RS, Chasens AL, Eisenberg R. The 144. Thitinanthapan W, Satamanont P, Vongsavan N. In vitro
influence of urea peroxide gel on plaque, calculus and penetration of the pulp chamber by three brands of car-
chronic gingival inflammation. J Periodontol 1973: 44: bamide peroxide. J Esthet Dent 1999: 11: 259–264.
636–639. 145. Thylstrup A, Ferjeerskov O. Clinical and pathological
125. Shellis RP. Transport processes in enamel and dentine. In: features of dental caries. In: Ferjeeskov C and Kidd E,
Addy M, Embery G, Edgar WM, Orchardson R, editors. editors. Textbook of clinical cariology, 2nd edn. Copen-
Tooth wear and sensitivity. London: Martin Dunitz, 2000: hagen, Denmark: Munksgaard, 1995: 2.
19–28. 146. Titley KC, Torneck CD, Smith DC, Chernecky R, Adibfar A.
126. Shields ED, Bixler D, El-Kafrawy AM. A proposed classi- Scanning electron microscopy observations on the pene-
fication for heritable dentine defects with description of a tration and structure on the resin tags in bleached and
new entity. Arch Oral Biol 1973: 18: 543–553. unbleached bovine enamel. J Endod 1991: 17: 72–75.
127. Singleton LS, Wagner MJ. Peroxide tooth whitener con- 147. Vallittu PK, Vallittu AS, Lassila VP. Dental aesthetics – a
centration versus composite resin etching. J Dent Res survey of attitudes in different groups of patients. J Dent
1992: 71: 281 (Abstract No. 1404). 1996: 24: 335–338.
128. Spasser HF. A simple bleaching technique using sodium 148. Victorin K. Review of genotoxicity of ozone. Mutat Res
perborate. NY Dent J 1961: 27: 332–334. 1992: 277: 221–238.
129. Sterrett J, Price RB, Bankey T. Effects of home bleaching 149. Vogel RI. Intrinsic and extrinsic discolouration of the
on the tissues of the oral cavity. J Can Dent Assoc 1995: 61: dentition. A review. J Oral Med 1975: 30: 99–104.
412–420. 150. Watts A, Addy M. Tooth discolouration and staining. A
130. Sulieman M, Addy M, MacDonald E, Rees JS. The effect review of the literature. Br Dent J 2001: 190: 309–316.
of hydrogen peroxide concentration on the outcome of 151. Weatherall JA, Robinson C, Hallsworth AS. Changes in the
tooth whitening: an in vitro study. J Dent 2004: 32: 295– fluoride concentration of the labial surface enamel with
299. age. Caries Res 1972: 6: 312–324.
131. Sulieman M, Addy M, MacDonald E, Rees JS. A safety 152. Weerheijm KL. Molar incisor hypomineralisation (MIH).
study in-vitro for the effects of an in-office bleaching Eur J Paediatr Dent 2003: 3: 115–120.
system on the integrity of enamel and dentine. J Dent 153. Weerheijm KL. Molar incisor hypomineralisation (MIH):
2004: 32: 581–590. clinical presentation, aetiology and management. Dent
132. Sulieman M, Addy M, MacDonald E, Rees JS. The Update 2004: 31: 9–12.
bleaching depth of a 35% hydrogen peroxide based in- 154. Weerheijm KL, Mejare I. Molar Incisor Hypomineralisa-
office product: a study in vitro. J Dent 2005: 33: 33–40. tion: a questionnaire inventory of its occurance in mem-

168
An overview of tooth-bleaching techniques

ber countries of the European academy of paediatric 159. Woolverton CJ, Haywood VB, Heymann HO. A toxico-
dentistry. Int J Paediatr Dent 2003: 13: 411–416. logical screen of two carbamide peroxide tooth whiteners.
155. Wei SH, Ingram MI. Analysis of the amalgam tooth J Dent Res 1991: 70: 558 (Abstract No. 2335).
interface using the electron microprobe. J Dent Res 1969: 160. Wright J, Robinson C, Shoe R. Characterisation of the
48: 317. enamel ultra structure and mineral content in hypoplastic
156. White DJ, Kozak KM, Duschner HH, Gotz H, Zoldaz JR. amelogenesis imperfecta. Oral Surg Oral Med Oral Pathol
Effects of whitening peroxide gels on exposed surface 1991: 72: 594–601.
dentine in vitro. Research presented at the 30th Annual 161. Zach L, Cohen G. Pulp response to externally applied
Meeting of the American Association for Dental Research, heat. Oral Surg, Oral Med, Oral Path 1965: 19: 515–530.
2001. 162. Zalkind M, Arwaz JR, Goldman A, Rotstein I. Surface
157. Wiktop CJ Jr. Amelogenesis imerfecta, dentinogenesis morphology changes in human enamel, dentin and
imperfecta and dentine dysplasia revisited: problems in cementum following bleaching: a scanning electron
classifications. J Oral Pathol 1988: 17: 547–553. microscope study. Endod Dent Traumatol 1996: 12: 82–84.
158. Winter GB. Anomalies of tooth formation and eruption. 163. Zekonis R, Matis BA, Cochran MA, Al Shetri SE, Eckert GJ,
In: Welbury RW, editor. Paediatric dentistry. Oxford, UK: Carlson TJ. Clinical evaluation of in-office and at-home
Oxford University Press, 1997: 266–270. bleaching treatments. Oper Dent 2003: 28: 114–121.

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