Treatment Options, Apexogenesis And Apexification.pdf

  • Uploaded by: Ion Bondari
  • 0
  • 0
  • December 2019
  • PDF

This document was uploaded by user and they confirmed that they have the permission to share it. If you are author or own the copyright of this book, please report to us by using this DMCA report form. Report DMCA


Overview

Download & View Treatment Options, Apexogenesis And Apexification.pdf as PDF for free.

More details

  • Words: 3,263
  • Pages: 4
Injuries to Permanent Dentition Symposium

Treatment Options: Apexogenesis and Apexification Shahrokh Shabahang, DDS, MS, PhD Abstract This article will describe requirements for case selection and review the procedures for apexogenesis and apexification in immature permanent teeth. Nonclinical and clinical data will be presented to support the recommendations, and outcomes will be presented from clinical studies. The dental pulp is an ectomesenchymally derived connective tissue with certain unique properties such as being encased in hard tissues, which limits its collateral circulation. The pulp provides a matrix for binding of its cells and provides support allowing communication between the cells. In addition to immune cells, the dental pulp contains odontoblasts, which are specialized cells capable of producing dentin. In the absence of a vital pulp, dentin deposition is arrested. When an immature tooth is affected by caries or trauma, the pulp requires proper management according to the degree of inflammation and its vitality. Maintenance of pulp vitality will allow continued root development along the entire root length. If the pulp is irreversibly inflamed or necrotic, root-end closure procedures are required when the apex has not fully formed. (J Endod 2013;39:S26–S29)

Key Words Apexification, apexogenesis, immature permanent teeth, treatment

From the Department of Endodontics, Loma Linda University, Loma Linda, California. This article is being published concurrently in Pediatric Dentistry 2013;35(2). The articles are identical. Either citation can be used when citing this article. Address requests for reprints to Dr Shahrokh Shabahang, 5 East Citrus Avenue, Suite 201, Redlands, CA 92373. E-mail address: [email protected] 0099-2399/$ - see front matter Copyright ª 2013 American Academy of Pediatric Dentistry and American Association of Endodontists. http://dx.doi.org/10.1016/j.joen.2012.11.046

S26

Shabahang

Role of the Dental Pulp in Tooth Development

T

he dental pulp contains immune cells that allow it to mount a response against offending irritants. The pulp also contains odontoblasts, which are specialized to form dentin. In the absence of a vital pulp, the tooth structure is susceptible to infection, and dentin deposition is arrested. Maintenance of pulp vitality is imperative in an immature permanent tooth to allow continued root development. The pulp tissue is removed when pathologically inflamed or necrotic. Although studies are underway to develop materials and techniques for pulp regeneration procedures, the purpose of this review is to provide an overview of apexogenesis and apexification in immature permanent teeth with pulpal pathosis.

Apexogenesis or Apexification Proper assessment of the affected tooth is critical in determining an accurate diagnosis and prescribing the appropriate treatment plan. Assessment of pulp vitality will aid in determining the proper treatment option. If vital and not irreversibly inflamed, maintenance of its vitality will allow natural continued root development. Figure 1 presents a flow chart to facilitate the decision-making process when treating permanent teeth with incomplete root development. Assessment of the tooth in question is made by using radiographic evaluation to determine the maturity of the developing root and clinical evaluation that is based on history and clinical testing. Obviously immature teeth are frequently associated with child patients. Pulp testing in children is a complex procedure and subjective in nature. Maintenance of pulp vitality by using apexogenesis will allow continued root development along the entire root length. Depending on the extent of inflammation, pulp capping, shallow pulpotomy, or conventional pulpotomy may be indicated. The dental pulp in young patients is more cellular and able to recover from injuries. Cvek et al (1) demonstrated that in teeth with complex crown fractures, the exposed pulp maintained its vitality for up to 7 days. In these teeth, only the most superficial 2 mm of the pulp is inflamed and requires removal. If pulpal necrosis occurs in immature teeth, an alternative treatment approach must be used because of the presence of an open apex (2). The young pulpless tooth frequently has thin, fragile walls, which makes it difficult to adequately clean and to obtain the necessary apical seal (2). Traditionally, the approach has been to use calcium hydroxide (CH) to induce apexification after disinfection of the root canals in the conventional manner (3). Completion of endodontic therapy was typically delayed until completion of root-end closure through apexification. Apexification is defined as ‘‘a method of inducing a calcified barrier in a root with an open apex or the continued apical development of an incompletely formed root in teeth with necrotic pulp’’ (4). The disadvantages of traditional, long-term CH therapy include variability in treatment time, unpredictability of formation of an apical seal, difficulty in following up patients, and delayed treatment. An alternative to CH therapy is placement of an apical plug. Several investigators have demonstrated the use of dentin apical plugs in nonsurgical root canal therapy of mature teeth (5–9). Mineral trioxide aggregate (MTA) is a material that may be best suited as an apical plug. In 1999, Shabahang et al (10) showed consistent barrier formation when MTA was used as an apical plug in an in vivo dog model with open apices. Several studies have confirmed successful clinical outcomes including healing of existing periapical lesions in majority of immature teeth that were treated with an MTA apical plug (11, 12).

JOE — Volume 39, Number 3S, March 2013

Injuries to Permanent Dentition Symposium used root canal irrigants (26, 27). MTAD is effective as a final rinse before obturation to disinfect the root canal system and to remove the smear layer. In 2001, Iwaya et al (28) published a case that demonstrated the effectiveness of a double antibiotic paste to disinfect a premolar with a necrotic pulp and a large periradicular radiolucent lesion. Three years later, Banchs and Trope (29) published a similar case. In this case report and subsequent studies, Trope’s group recommended a mixture of metronidazole, ciprofloxacin, and minocycline. In in vitro studies this antibiotic combination has demonstrated the potential to disinfect the root canal system (30).

Treatment Outcomes Figure 1. Case selection for treatment of permanent teeth with incomplete root development.

The advantages of using an apical plug include requirement for fewer appointments to complete the treatment, more predictable apical barrier formation, and reduced need for patient follow-up appointments. The disadvantage of this technique is that, similarly to CH therapy, it only addresses the apical opening and does not account for complete root development along the entire root length. Regardless of the technique used, a critical step in treatment of pulpless teeth with open apices is proper debridement and disinfection of the canal space.

Disinfection Protocols Immature permanent teeth pose special challenges during endodontic procedures not only because of the wide-open root apex but also because of the thin dentin walls. Therefore, debridement is completed primarily by chemical means to remove any remaining pulp tissues and for disinfection. Furthermore, an accurate determination of root length is required to ensure complete canal debridement and to confine treatment materials to the canal space to avoid damaging the very valuable remnants of the Hertwig epithelial root sheath. Generally, electronic apex locators are not accurate in teeth with wide-open apices (13). Radiographic root determination is the best means to obtain accurate root length measurement. Sodium hypochlorite (NaOCl) and CH have excellent tissuedissolving properties as well as antimicrobial efficacy (14–18). Whereas NaOCl exerts its effect during the course of the procedure, CH requires additional exposure time. A 1-week obturation of the canal space with CH will allow disinfection along with dissolution and removal of pulpal remnants (19). Despite its convenient availability, several investigators have reported shortcomings with respect to NaOCl’s ability to completely disinfect the root canal space (20–22). Long-term exposure to CH may also have detrimental effects on dentin. Studies have shown that long-term CH therapy that would expose root dentin to CH for periods exceeding 1 month results in structural changes in the dentin, with higher susceptibility to root fracture (23, 24). Use of antibiotics has also been documented during the past years and is regaining popularity in recent years. In 1980, Das (25) reported successful apexification of a tooth after root canal debridement and intracanal antibiotic therapy with an oxytetracycline HCl ointment. In 2003, Torabinejad and his group published a series of reports to demonstrate the advantages of a mixture of doxycycline, citric acid, and detergent (BioPure MTAD; DENTSPLY Tulsa Dental Specialties, Tulsa, OK) over NaOCl and other commonly JOE — Volume 39, Number 3S, March 2013

Nonclinical and clinical studies have reported good results with a variety of techniques. The most significant shortcoming of longterm CH therapy is the length of time required to complete treatment and frequent challenges in following up with patients over time. A root fracture at the cervical region is a common cause of failure in these cases. Thin dentin at the cervical region and changes in the dentin structure resulting from long exposure times to CH are the causative factors. Table 1 summarizes the outcome results from several studies. Depending on the study, the speed of barrier formation by using CH therapy varies from 3 to 24 months (2, 31). The suggested time to change the CH in the canal varies from once every 3 months, once every 6–8 months, or not at all (31–33). Torneck and Smith (34) have indicated that there may be incomplete bridging of the apex, even though a two-dimensional radiograph may give the appearance of complete bridge formation. Periradicular inflammation may persist around the apices of many teeth because of the presence of necrotic tissue in the irregularities of the apical bridge. Therefore, the presence of a radiographically and clinically closed apex is not necessarily indicative of a normal periodontium (35). Another major drawback of the apexification protocol that uses CH is the effect that a long-term application of CH has on the structural integrity of the root dentin. Several studies have demonstrated that with longer exposures of dentin to CH, its ability to resist fracture is significantly decreased (23, 36). In a systematic review and meta-analysis comparing the outcomes of CH apexification and MTA apical plug, the authors concluded that the clinical success of both procedures was the same (37). On the basis of the combined data of the 2 studies, the difference in clinical success between the 2 treatment regimens was not statistically significant. Overall, the results of several studies show that MTA plugs are effective in treating immature permanent teeth with necrotic pulps. The advantages of apexification that uses an MTA plug are reduced treatment time and a more predictable barrier formation. The shortcoming, similar to CH therapy, is that placement of an apical plug does not account for continued root development along the entire root length. Complete root development requires a viable pulp containing cells that can differentiate into dentin-producing odontoblasts. For this, ongoing studies are aiming to identify procedures and materials that allow pulp regeneration. The dental pulp is complex with a variety of cells, nerves, and blood vessels. To regenerate this organelle, it is important to keep in mind the required prerequisites, including cells that are capable of differentiating into pulp cells, the proper signal that is required for the differentiation, and an appropriate scaffold that is suitable for guiding regeneration of the desired tissues, while keeping out the faster growing osseous tissues.

Apexogenesis and Apexification

S27

Shabahang

Technique/material

Investigator(s)

No. of cases

Observation

JOE — Volume 39, Number 3S, March 2013

CH therapy CH therapy CH therapy

Heithersay, 1970 Ghose et al, 1987 Morfis and Siskos, 1991

21 43 34

14–75 months 3–10 months

CH therapy CH therapy

Lee et al, 2010 Walia et al, 2000

32 15

10–14 weeks

CH therapy

Dominguez Reyes et al, 2005

26

Average time 12.19 months

CH therapy

Mendoza et al, 2010

28

Comparison of MTA plug with CH therapy Comparison of MTA plug with CH therapy

El-Meligy and Avery, 2006

15

3.24–13.96 months (mean 8.6 months) 12 months

Pradhan et al, 2006

20

8 months

MTA plug

Pace et al, 2007

11

2 years

MTA plug MTA plug MTA plug MTA plug MTA plug MTA plug

Erdem and Sepet, 2008 Sarris et al, 2008 Holden et al, 2008 Nayar et al, 2009 Annamalai and Mungara, 2010 Moore et al, 2011

5 17 20 38 30 22

MTA plug MTA plug

Simon et al, 2007 Witherspoon et al, 2008

43 78

2 years 11.7 years 12–44 months 12 months 12 months Mean follow-up time 23.4 months 12 months Mean recall time was 19.4 months

A PubMed search was conducted in August 2012 to identify citations with CH, MTA, apical plug, outcomes, and clinical studies.

Outcomes Apical canal seen radiographically, but no apical barrier clinically 49 of 51 developed an apical barrier Continued root development in 6 cases, continued root development and bridge formation in 3 cases, bridge formation in 21 cases, and in 4 cases no root-end closure Apical closure in necrotic cases with or without lesion 100% apical closure with porous barrier. Older children with narrow apex had shorter time; teeth without periapical infection showed faster results. Apical closure obtained in 100% of cases; 88.4% needed 3–4 sessions (average of 3.23 sessions) Cementoid tissue (85.72%) or osseous tissue (14.28%) 2 of CH teeth had become reinfected, but all teeth treated with MTA plug remained successful Periapical lesions resolved in 4.6  1.5 months for MTA group and in 4.4  1.3 months for CH group. Total treatment was completed in 0.75  0.5 months for MTA group and 7  2.5 months for CH group. 10 of 11 cases healed, and remaining case considered incomplete healing 4 of 5 teeth healed; 1 case in MTA was extruded 94.1% clinical success, 76.5% radiographic success; 17.6% uncertain Healing rate was 93.75% All teeth were clinically and radiographically successful 100% success clinically and radiographically Clinical and radiographic success rate of 95.5%; discoloration in 22.7% of teeth 81% healed 93.5% of teeth treated in 1 visit healed, and 90.5% of teeth treated in 2 visits healed

Injuries to Permanent Dentition Symposium

S28 TABLE 1. Outcomes of Clinical Studies with CH Therapy and MTA Apical Plug

Injuries to Permanent Dentition Symposium Acknowledgments The author denies any conflicts of interest related to this study.

References 1. Cvek M, Cleaton-Jones PE, Austin JC, Andreasen JO. Pulp reactions to exposure after experimental crown fractures or grinding in adult monkeys. J Endod 1982;8:391–7. 2. Frank AL. Therapy for the divergent pulpless tooth by continued apical formation. J Am Dent Assoc 1966;72:87–93. 3. Seltzer S. The root apex. In: Seltzer S, Krasner P, eds. Endodontology: Biologic Considerations in Endodontic Procedures. Malvern, PA: Lea & Febiger; 1988:1–30. 4. Sheely EC, Roberts GJ. Use of calcium hydroxide for apical barrier formation and healing in non-vital immature permanent teeth: a review. Br Dent J 1997;183: 241–6. 5. Tronstad L. Tissue reactions following apical plugging of the root canal with dentin chips in monkey teeth subjected to pulpectomy. Oral Surg Oral Med Oral Pathol 1978;45:297–304. 6. Holland R, De Souza V, Nery MJ, et al. Tissue reactions following apical plugging of the root canal with infected dentin chips: a histologic study in dogs’ teeth. Oral Surg Oral Med Oral Pathol 1980;49:366–9. 7. Holland R, Nery MJ, Souza V, et al. The effect of the filling material in the tissue reactions following apical plugging of the root canal with dentin chips: a histologic study in monkeys’ teeth. Oral Surg Oral Med Oral Pathol 1983;55:398–401. 8. Holland GR. Periapical response to apical plugs of dentin and calcium hydroxide in ferret canines. J Endod 1984;10:71–4. 9. Brady JE, Himel VT, Weir JC. Periapical response to an apical plug of dentin filings intentionally placed after root canal overinstrumentation. J Endod 1985;11:323–9. 10. Shabahang S, Torabinejad M, Boyne PJ, et al. A. comparative study of root-end induction using osteogenic protein-1, calcium hydroxide, and mineral trioxide aggregate in dogs. J Endod 1999;24:1–5. 11. Holden DT, Schwartz SA, Kirkpatrick TC, Schindler WG. Clinical outcomes of artificial root-end barriers with mineral trioxide aggregate in teeth with immature apices. J Endod 2008;34:812–7. 12. Moore A, Howley MF, O’Connell AC. Treatment of open apex teeth using two types of white mineral trioxide aggregate after initial dressing with calcium hydroxide in children. Dent Traumatol 2011;27:166–73. 13. Hulsmann M, Pieper K. Use of an electronic apex locator in the treatment of teeth with incomplete root formation. Endod Dent Traumatol 1989;5:238–41. 14. The SD. The solvent action of sodium hypochlorite on fixed and unfixed necrotic tissue. Oral Surg Oral Med Oral Pathol 1979;47:558–61. 15. Cunningham WT, Balekjian AY. Effect of temperature on collagen-dissolving ability of sodium hypochlorite endodontic irrigant. Oral Surg Oral Med Oral Pathol 1980; 49:175–7. 16. Cunningham WT, Joseph SW. Effect of temperature on the bactericidal action of sodium hypochlorite endodontic irrigant. Oral Surg Oral Med Oral Pathol 1980; 50:569–71. 17. Morgan RW, Carnes DL Jr, Montgomery S. The solvent effects of calcium hydroxide irrigating solution on bovine pulp tissue. J Endod 1991;17:165–8.

JOE — Volume 39, Number 3S, March 2013

18. Baumgartner JC, Cuenin PR. Efficacy of several concentrations of sodium hypochlorite for root canal irrigation. J Endod 1992;18:605–12. 19. Sj€ogren U, Figdor D, Sp angberg L, Sundqvist G. The antimicrobial effect of calcium hydroxide as a short-term intracanal dressing. Int Endod J 1991;24:119–25. 20. Shabahang S, Pouresmail M, Torabinejad M. In vitro antimicrobial efficacy of MTAD and sodium hypochlorite. J Endod 2003;29:450–2. 21. Waltimo T, Trope M, Haapasalo M, Ørstavik D. Clinical efficacy of treatment procedures in endodontic infection control and one year follow-up of periapical healing. J Endod 2005;31:863–6. 22. Siqueira JF Jr, Rocas IN. Clinical implications and microbiology of bacterial persistence after treatment procedures. J Endod 2008;34:1291–301. 23. Andreasen JO, Farik B, Munksgaard EC. Long-term calcium hydroxide as a root canal dressing may increase risk of root fracture. Dent Traumatol 2002;18: 134–7. 24. Hatibovic-Kofman S, Raimundo L, Zheng L. Fracture resistance and histological findings of immature teeth treated with mineral trioxide aggregate. Dent Traumatol 2008;24:272–6. 25. Das S. Apexification in a nonvital tooth by control of infection. J Am Dent Assoc 1980;100:880–1. 26. Torabinejad M, Khademi AA, Babagoli J, et al. A new solution for the removal of the smear layer. J Endod 2003;29:170–5. 27. Torabinejad M, Shabahang S, Aprecio R, Kettering JD. The antimicrobial effect of MTAD: an in vitro investigation. J Endod 2003;29:400–3. 28. Iwaya SI, Ikawa M, Kubota M. Revascularization of an immature permanent tooth with apical periodontitis and sinus tract. Dent Traumatol 2001;17:185–7. 29. Banchs F, Trope M. Revascularization of immature permanent teeth with apical periodontitis: new treatment protocol? J Endod 2004;30:196–200. 30. Hoshino E, Kurihara-Ando N, Sato I. In-vitro antibacterial susceptibility of bacteria taken from infected root dentine to a mixture of ciprofloxacin, metronidazole and minocycline. Int Endod J 1996;29:125–30. 31. Finucane D, Kinirons MJ. Non-vital immature permanent incisors: factors that may influence treatment outcome. Endod Dental Traumatol 1999;15:273–7. 32. Chosack A, Sela J, Cleaton-Jones P. A histological and quantitative histomorphometric study of apexification of nonvital permanent incisors of vervet monkeys after repeated root filling with a calcium hydroxide paste. Endod Dent Traumatol 1997;13:211–7. 33. Abbott PV. Apexification with calcium hydroxide: when should the dressing be changed? the case for regular dressing changes. Aust Endod J 1998;24: 27–32. 34. Torneck CD, Smith J. Biologic effects of endodontic procedures on developing incisor teeth: I—effect of partial and total pulp removal. Oral Surg Oral Med Oral Pathol 1970;30:258–66. 35. Koenigs JF, Heller AL, Brilliant JD, et al. Induced apical closure of permanent teeth in adult primates using a resorbable form of tricalcium phosphate ceramic. J Endod 1975;1:102–6. 36. Rosenberg B, Murray PE, Namerow K. The effect of calcium hydroxide root filling on dentin fracture strength. Dent Traumatol 2007;23:26–9. 37. Chala S, Abouqal R, Rida S. Apexification of immature teeth with calcium hydroxide or mineral trioxide aggregate: systematic review and meta-analysis. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2011;112:e36–42.

Apexogenesis and Apexification

S29

Related Documents


More Documents from ""

December 2019 9
December 2019 11
Dental Caries Booklet.pdf
December 2019 18
Nomenclature.pdf
June 2020 9
Homo.oeconomicus.doc
December 2019 28