Apexification 07.03.22
Apexification 07.03.22
Discussion:
Apexification, apexogenesis, and revascularization techniques are all alternatives for treating
an open apex. Apexogenesis is a procedure that preserves important pulpal tissue in the apical
section of a root canal, allowing the root apex to form completely.(14)As a result,
apexogenesis can only occur if some essential pulp remains. It was not practicable, in all the
above cases, because the teeth had necrotic pulps. Revascularization has been considered as
an alternative treatment in some situations of inadequate root development because it
encourages the thickness and apical closure of juvenile teeth,. (15)(16) Revascularization, on
the other hand, has the potential for favourable clinical and biological consequences.
However certain disadvantages like the discoloration of the crown (17), development of
bacterial strains that are resistant to antibiotics, and an allergic response to intracanal
medicaments may be present. (18). Furthermore, the process of pulpal revascularization, the
tissue type that has formed on the walls of root canal, and the therapeutic implications of
follow-up for long periods remain unknown and under investigation. In the light of these
considerations, a treatment plan which is a more predictable (apexification) was chosen in the
current circumstances Most apexification treatments involving human young permanent teeth
assosciated with apical periodontitis need the placement of an apical plug to seal the tooth
and prevent bacterial leakage. (19)
The traditional calcium hydroxide apexification treatment takes at least three to four months,
with an average of six months, and requires many appointments. Patient adherence to this
lengthy treatment plan may be low, and many patients fail to show up for planned
appointments. The ultimate goal of the treatment described for such patients is to construct a
barrier apically in a single visit that will prevent toxic products and bacterial components
from the root canal from penetrating into the tissues periapically. This barrier is also
necessary for root filling material compaction on a technical level. (20)
Because of its superior biocompatibility and sealing capabilities, MTA is becoming the key
choice of material for apexification therapy since its discovery by Torabinejad et al. (21). It is
employed in pulp capping, pulpotomy practice, and closing ledges in the root canal (22). For
the immature apex, single-visit apexification is the best reasonable treatment option
presently. MTA is a bioactive cement that can stimulate the creation of new cementum and
PDL, making it biologically suitable for canal closure with an immature open apex. (23)
MTA works by releasing Ca2 ions, which stimulate cellular adhesion and cellular proliferation
while also creating an antimicrobial environment due to the high pH.. CaSiO4, Bi₂O₃,
CaCO3, CaSO₄, and calcium aluminate are the main primary ingredients and it includes a
hydrophilic powder that reacts with water to produce calcium hydroxide and hydrated
CaSiO4 gel. According to Holland et al, MTA's tricalcium oxide reacts with tissue fluids to
form calcium hydroxide, which forms an apical barrier. (24). Apart from poor handling
features, discoloration possibility (Gray MTA), limited washout resistance, and expensive
material cost, ProRoot MTA's long setting time are some of the important issues. (25)(26).
However, MTA causes substantially more consistent apical hard tissue development than
compared to CH. A systematic evaluation evaluating the MTA and CH effectiveness as
materials for the apexification of juvenile teeth found no significant differences in the success
or apical barrier creation between the two groups. Although the time it took for immature
teeth treated with MTA to generate apical biological calcified barriers was much less than for
those treated with CH, MTA and CH were evaluated clinically & radiographically as agents
to induce apexification for 15 children, each with two infected immature permanent teeth, by
Eli-Meligy and Avery (28)(29). Only two of the CH-treated teeth failed after a year due to
chronic periradicular inflammation and pain on percussion. There was no clinical or
radiographic pathology in any of the MTA-treated teeth. In none of the groups, the relative
thickness of the dentinal walls was increased. These findings are consistent with those of
Shah et al. (28), he found that only the root surface was coated with newly formed
mineralized tissue. However, there are a few drawbacks, such as long setting periods (MTA
has a 70-minute initial setting time and a 175-minute final setting time.), handling difficulties,
and the possibility of coronal staining, as well as the high cost of MTA (9), compared to
biodentin.
Biodentine is a new dentin substitute cement that is bioactive. In powder form, it is composed
of tricalcium silicate, dicalcium silicate, calcium carbonate, calcium oxide, zirconium oxide,
and CH.. A water-soluble polymer and calcium chloride make up the liquid for mixing with
the cement powder, which speeds up the setting process. (29)
In comparison to MTA, which takes 2 hours and 45 minutes to set, Biodentine takes only 12
minutes. Biodentine is bioactive, according to Zanini et al. (12), since it causes odontoblast-
like cells to differentiate and promotes the proliferation and biomineralization of the murine
pulpal cells. The reaction of pulp to direct biodentine capping demonstrated the creation of a
full dentine bridge and a thin layer of odontoblast-like cells beneath the osteodentin. (30)
Biodentine has demonstrated to be non-cytotoxic and to increase the creation of collagen
fibers and fibroblasts. Biodentine, unlike MTA, has the drawback of being unable to be
employed in the presence of moisture. On radiographic examination, it was discovered that
teeth treated with biodentine had improved early periapical healing. On the other hand, better
long-period healing of MTA-filled teeth was observed periapically. It could be because MTA
has better marginal adaptability. (31)
Many researchers have shown that a fibroblast cell line can survive in the presence of
Biodentine and MTA. After 24 hours, scanning electron microscopy revealed that cells
attached to most Biodentine surfaces. (32). Human gingival fibroblasts sensitized to
Biodentine and MTA adhered and diffused to the material surface after 7 days in culture,
according to Zhou et al. (33) The biocompatibility of biodentine also has been demonstrated
in human bone marrow stem cells. In human bone marrow stem cells, this biomimetic cement
increased the expression of runt-related transcription factor 2 and promoted osteogenic
development. (34)
Several writers present case studies of apexification treatments in young immature permanent
teeth using a Biodentine apical plug. After 1 month of CH dressing. Biodentine was used as
an apical barrier, while a synthetic collagen membrane was used as a matrix, by Nayak and
Hasan (35), reported the first case. Sinha et al. (36) employed a triple antibiotic paste for a
week in the root canal before putting in a Biodentine apical plug. A 12-month cone-beam
computed CT follow-up revealed gradual reduction of periapical radiolucency, as well as
revealation of excellent periapical tissue repair and a lack of clinical complaints. A single-
visit apexification surgery with Biodentine on a traumatically wounded tooth indicated This
biological and biocompatible calcium-based cement has the potential to cure injured tooth
tissues, making it a viable alternative to multiple-visit apexification. (37) In all cases, the
apical barrier was 5 mm thick, and the canals were retro-filled with gutta-percha and a resin-
based sealant. According to Camilleri et al. (5), Biodentine outperforms MTA in terms of
mechanical properties and biocompatibility because its consistency is better suited to clinical
use, ensuring better handling and safety. The material does not require multiple-step
obturation, and the setting is faster, reducing the risk of bacterial contamination. (13).
Biodentine, on the other hand, may have a disadvantage in terms of radiopacity (12).
MTA and Biodentine both have excellent sealing characteristics, according to comparative
investigations, reducing the danger of microbial contamination in the future. (30) Biodentine
and MTA may be effective apexification materials, as evidenced by the positive clinical and
radiological outcomes in these cases.
Conclusion
Apexification in a single visit using biocompatible materials like Biodentine and MTA can be
a successful treatment option for teeth with open apices. Based on the aforementioned case
studies, it can be concluded that while MTA has superior radiopacity contrast, it is more
expensive, takes longer to set, has a higher risk of discoloration, and is more difficult to
handle.
It does, however, have excellent micro sealing abilities. Biodentin, on the other hand, has a
lower radiopacity, making it more difficult to locate in radiographs at times, but it also has a
lower cost, better biocompatibility, and a very quick setting time, allowing gutta-percha
obturation on the same day, implying that both materials have few advantages over each
other and can be used as needed.
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