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Revista odontológica mexicana

versión impresa ISSN 1870-199X

Rev. Odont. Mex vol.18 no.1 Ciudad de México ene./mar. 2014

 

Case report

 

Multi-disciplinary treatment of female patient afflicted with generalized aggressive periodontitis and type 1 diabetes mellitus

 

Evelyn Vásquez Ciriaco,* María del Carmen López Buendía §

 

* Graduate, Implantology and Periodontics Specialty.

§ Professor, Implantology and Periodontics Specialty.

Graduate and Research School, National School of Dentistry, National University of Mexico (UNAM).

 Correspondence

 

ABSTRACT

The impact of systemic diseases on oral health has been well documented. Certain systemic disorders can modify the host's immune response to periodontal pathogens, thus exacerbating the severity of the periodontal disease. Among systemic diseases, uncontrolled diabetes mellitus is associated to periodontal disease. Aggressive periodontitis can appear in young adults and elicit rapid destruction of the periodontal insertion apparatus. Severe loss of periodontal support present in these cases hinders prognosis of affected teeth, and thus, the clinician faces complications when designing treatment plans and deciding upon extraction or non extraction of compromised teeth. Accomplishment of comprehensive treatment requires participation of other fields of dentistry. The aim of the present study was to present the multi-disciplinary treatment of a 17-year-old female patient afflicted with type 1 diabetes mellitus and generalized aggressive periodontitis, and present results obtained one year after completion of treatment.

Key words: Aggressive periodontitis, type 1 diabetes mellitus, periodontal disease, multi-disciplinary treatment.

 

INTRODUCTION

Diabetes mellitus (DM) is caused by an insulin-dependent glucose metabolism alteration, as well as by lipid metabolism. Classical symptoms are: polydipsia, polyuria and polyphagia; frequently accompanied by chronic fatigue and weight loss. Diabetes mellitus complications include retinopathy, nephropathy neuropathy and cardiovascular diseases. Association between DM and periodontal disease has been extensively discussed in scientific literature.1 Some authors2,3 have diagnosed cases of aggressive periodontitis in patients with systemic diseases such as congenital neutropenia, Chediak-Higashi syndrome or diabetes mellitus. An analysis conducted by the National Health and Nutrition Examination Survey confirmed the fact that prevalence of periodontitis was significantly higher in diabetic patients when compared to non-diabetic ones (17.3 versus 9 %).1 Many studies on epidemiology have reported the fact that severity and extension of periodontal disease is greater in uncontrolled diabetes mellitus patients when compared to healthy patients. These studies also report that periodontitis manifestations vary within the diabetic population. This is due to differences in studied populations.4,5 The main oral manifestations exhibited by non-controlled diabetes mellitus patients are the following: increase in periodontal disease severity and edentulism in most patients over 40 years of age.6

Other authors suggest that type 1 and 2 diabetes mellitus are associated to increase in susceptibility to periodontal disease. Nevertheless, the response of healthy and diabetic patients to surgical and non-surgical periodontal therapy has been shown to be similar.7,8

By definition, aggressive periodontitis affects young subjects and is characterized by presenting constant rapid-progression episodes; the amount of microbial deposits is inconsistent with the periodontal destruction severity. It can appear as a localized or generalized condition. It exhibits familial tendency and is associated to the presence of Actinobacillus actinomycetemcomitans and Porphyromonas gingivalis, as well as abnormal neutrophil function.9,10 In young adults aggressive periondontitis cases, ethnic and genetic factors play an important role.11 Prevalence of localized aggressive periodontitis in European populations varies from 0.1 to 0.2% among adolescents and young adults; prevalence in African-American populations is 10%. Hispanic populations exhibit 5%, and Caucasian population in the USA shows a 1.3% prevalence.11 Severe loss of periodontal support observed in aggressive periodontitis cases hinders the process of deciding upon extraction or non extraction of compromised teeth.12 Some authors emphasize upon infection and inflammation control to improve results of the condition.13,14 Nevertheless when treating patients with generalized aggressive periodontitis, conventional mechanical therapy along with oral hygiene are frequently not sufficient to control the disease.15

Use of systemic antibiotics as part of aggressive periodontitis treatment has been supported in systematic reviews. Among broad spectrum antibiotics, we found that the combination of amoxicillin with metronidazole is effective to suppress Actinobacillus actinomycetemcomitans. Thisis probably due to the synergic effect which has been demonstrated in vitro when using a combination of both.16 Other antibiotics recommended for aggressive periodontitis treatment are: clindamycin, clavulanic acid, ciprofloxacin, tetracycline, azithromycin and tetracycline fibers.12,15-19

Within the realm of surgical therapy methods, there are different types of materials to correct bone defects. In the case of aggressive periodontitis treatment, some authors13 suggest use of different regeneration materials. One of them is the use of guided tissue regeneration technique (GTR). Several clinical studies have shown the success of guided tissue regeneration treatment in reconstructive periodontal surgery. After the systematic review20 of GTR use in bone defects, it can be concluded that this technique is more effective than the clinical gain of insertion levels and decrease of pocket depth when compared with conventional flap debridement surgery.

Bone grafts are another material used for the regeneration of periodontal bone defects. There is a great variety of grafts. In general terms, and according to aim analysis,21 it was concluded that defects treated with bone grafts exhibited increase of the bone level, decrease (reduction) of alveolar crest loss, increase of insertion levels and decrease of probing depth when compared to the conventional technique of flap debridement. No clinical differences have been observed among different types of grafts (particulated allograft, calcium phosphate and ceramic grafts). When combined with membranes, the gain of clinical insertion levels was increased, and the probing depth was decreased when compared with results achieved with the use of solely grafts. Within the great variety of existing materials used for periodontal regeneration, we find plasma rich in growth factors (PRGF)22 which has shown beneficial effects. According to clinical results PRGF increases and accelerates bone regeneration, and soft tissue healing is more rapid and predictable.

The aim of the present study was to present the multi-disciplinary treatment of a 17 year old female patient, afflicted with type 1 diabetes mellitus and generalized aggressive periodontitis, as well as to record results one year after completion of treatment.

 

CLINICAL CASE

17 year old female patient, with insulin-controlled type 1 diabetes mellitus history, since the age of 12, who attended the Periodontics Department of the Research and Graduate School of the National School of Dentistry (UNAM). The patient's complaint was pain upon mastication (Figure 1).

Clinical exploration revealed deficient oral hygiene, grade II and III dental mobility (teeth were splinted with orthodontic devices), plaque accumulation, multiple periodontal abscesses, suppuration, spontaneous bleeding, intensely swollen and edematous gums, presence of calculi and periodontal pockets with 8 mm minimum depth (Table I).

Dental history revealed absence of caries or previous dental treatment. When interviewed, the mother informed that her daughter had been diagnosed with periodontitis ten years before and had experienced early tooth loss.

Intra-oral radiographic series revealed severe bone loss in most teeth, with floating teeth appearance, as well as broadening of the periodontal ligament space around all the teeth (Figure 2).

Physical examination was non-contributory. Initial glycemia revealed poor glucose metabolic control, 220 mg/dL. Thus, the patient was remitted to the endocrinologist to achieve optimum glycemia control. Diagnosis emitted was generalized aggressive periodontitis and type 1 diabetes mellitus.

From the first visit, the patient and her mother were educated in diabetes management and oral health. An endocrinologist controlled the patient's glycemia in subsequent appointments.

 

TREATMENT

Treatment consisted of a periodontal phase 1 in which the following was accomplished: personal plaque control, brushing and dental floss techniques, and thereafter continued with root scarping and planning of all teeth. Endodontics and Oral Prosthesis Departments were consulted in order to tailor a comprehensive treatment plan. Upon completion of phase 1 the patient was prescribed amoxicillin with metronidazole for 7 days. During phase 2 all teeth exhibiting poor prognosis were extracted. (17, 16, 12, 11, 21, 22, 26, 27, 37, 36, 46, 47, 48). Process regularization and placement of free flap (onlay type) were undertaken in the upper anterior area in order to avoid ridge collapse. 4-0 vicryl was used for suturing. All along this period, the patient was subjected to antibiotic coverage (Figure 3).

Upon completion of surgery, upper and lower provisional removable prostheses were put into place. During the next surgery, flap debridement was achieved in lower teeth (35, 34, 33, 32, 31, 41, 42, 43, 44, 45). PRGF and auto-graft were applied, suture was performed with isolated 4-0 vicryl stitches (Figure 4).

Later on, surgery was performed with GTR and auto-graft in teeth 23, 24, 25 as well as flap debridement in teeth 13, 14, 15 (Figure 5).

Work was undertaken with collaboration from Oral Prosthesis and Endodontics Departments. Teeth number 13 and 23 were subjected to root canal treatment before surgery. Acrylic provisional prostheses were placed on teeth 15, 14, 13, 23, 24 and 25 in order to build splinted abutments. The patient was instructed on antibiotic and analgesic use according to the type of surgery performed.

After 8 months had elapsed from the last surgery, the prosthesis department built final restorations.

Upon completion of treatment the patient was subjected to a maintenance phase (Figure 6).

 

RESULTS

Final laboratory tests revealed 140 mg/dL glycemia control (compared to 220 mg/dL initial figures. Periodontal treatment elicited no complications and metabolic diabetes control brought about significant improvement in periodontal circumstances. Clinical change was significant. Assessment after one year revealed absence of inflammation clinical signs, reduction in periodontal pocket depth as well as 13% dental-bacterial plaque percentage. Tooth mobility decreased in all remaining teeth where grade 1 mobility was observed. A multi-disciplinary treatment was achieved with the participation of the endocrinologist, oral prosthesis department and the endodontics department, in order to attain successful and comprehensive oral rehabilitation.

 

DISCUSSION

There is ample discussion with respect to the presence of aggressive periodontitis associated to diabetes mellitus. Parameters of the American Periodontics Academy9 indicate that most patients with aggressive periodontitis are healthy; nevertheless, some publications point out an association of aggressive periodontitis with systemic conditions such as diabetes mellitus.2,23

There equally is controversy with respect to the manner in which to treat aggressive periodontitis. In 2001, Kai P. Worch, in a case report, stabilized aggressive periodontitis by means of combining root planning and scraping with systemic antibiotic coverage. Soete & et al, when using full mouth disinfection protocol established by Quirynen & et al, significantly decreased pocket depth and achieved clinical insertion gain in aggressive periodontitis patients. Other clinical operators such as Dodson & et al, stressed the use of regenerative materials combined with antibiotics for aggressive periodontitis treatment. There is a great variety of antibiotics suitable for aggressive periodontitis treatment. Selection criteria remain unclear. Antibiotic selection must be based upon patient-related factors as well as disease-related factors. In the present clinical case antibiotic coverage was deemed convenient, since it was observed that conventional periodontal treatment by itself did not elicit a favorable response.

Some authors like Debora C Rodriguez and Mario Taba Jr expressed in their publication the fact that non-surgical periodontal therapy allows the decrease of glycated hemoglobin levels, especially in patients afflicted with severe diabetes mellitus and periodontal disease. Nevertheless, up to the present date, in these cases, it has not been possible to determine clinical stability.

Regardless of all existing fashions to treat aggressive periodontitis, prognosis depends upon the following factors: whether the disease is localized or generalized, degree of destruction present at diagnosis time as well as the operator's skill to control future progression.12

 

CONCLUSIONS

One of the most important aspects of periodontal treatment success is educating the patient with respect to the disease, including cause, risk factors and the patient's role in the course of treatment.

In this patient afflicted with generalized aggressive periodontitis, the combination of mechanical, antimicrobial and surgical therapies as well as a suitable maintenance phase achieved stabilization of periodontal health. Appropriate glycemia control was also contributive to treatment results. Participation of medical areas and other dental areas was necessary for achievement of comprehensive and successful patient treatment.

 

REFERENCES

1. Aubrey SW, Avigdor K. The relationship between periodontal diseases and diabetes : an overview. Ann Periodontol. 2001; 6: 91-98.         [ Links ]

2. De Vree H, Steenackers K, Boever JA. Periodontal treatment of rapid progressive periodontitis in 2 siblings with papillon-Lefevre syndrome:15-year follow up. J Clin Periodontol. 2000; 27: 354-360.         [ Links ]

3. Bodur A, Bodur H, Bal B, Balos K. Generalized aggressive periodontitis in a prepubertl patient: A case report. Quintessence Int. 2001; 32: 303-308.         [ Links ]

4. Tervonen T, Oliver RC. Long-term control of diabetes mellitus and periodontitis. J Clin Periodontol. 1993; 20: 431-435.         [ Links ]

5. Campus G, Salem A, Uzzau S, Baldoni E, Tonolo G. Diabetes and periodontal disease: a case-control study. J Periodontol. 2005; 76: 418-425.         [ Links ]

6. Murrah VA. Diabetes mellitus and associated oral manifestations: a review. Journal of Oral Pathology. 1985; 14: 227.         [ Links ]

7. Gustke CJ. Treatment of periodontitis in the diabetic patient. J Clin Periodontol. 1999; 26: 133-137.         [ Links ]

8. American Academy of Periodontology. Parameter on periodontitis associated with systemic conditions. J Periodontol. 2000; 71: 876-879.         [ Links ]

9. American Academy of Periodontology. Parameters of care supplement. Parameter on aggressive periodontitis. J Periodontol. 2000; 71: 867-869.         [ Links ]

10. Hilgers KK, Dean JW, Mathieu GP. Localized aggressive periodontitis in a six-year-old: a case report. Pediatr Dent. 2004; 26: 345-351.         [ Links ]

11. Levin L, Baev V, Lev R, Stabholz A, Ashkenazi M. Aggressive periodontitis among young israeli army personnel. J Periodontol. 2006; 77: 1392-1396.         [ Links ]

12. Klokkevold RP, Newman GM, Takei H, Carranza AF. Treatment of aggressive and atypical forms of periodontitis. 11th ed. In: Carranza's Clinical Periodontology. E.U.: Elsevier; 2006: pp. 693-700.         [ Links ]

13. Mengel R, Soffner M, Flores-de-Jacoby L. Bioabsorbable membrane and bioactive glass in the treatment of intrabony defects in patients with generalized aggressive periodontitis: results of a 12-month clinical and radiological study. J Periodontol. 2003; 74: 899-908.         [ Links ]

14. Jaffin RA, Greenstein G, Berman CL. Treatment of juvenile periodontitis patients by control of infection and inflamation. J Periodontol. 1984; 55 (5): 261-267.         [ Links ]

15. Purucker P, Mertes H, Goodson JM, Bernimoulin JP. Local versus systemic adjunctive antibiotic therapy in 28 patients with generalized aggressive periodontitis. J Periodontol. 2001; 72: 1241-1245.         [ Links ]

16. Guerrero A, Griffiths GS, Nibali L, Suvan J, Moles DR, Laurell L et al. Adjunctive benefits of systemic amoxicillin and metronidazole in non-surgical treatment of generalized aggressive periodontitis: a randomized placebo-controlled clinical trial. J Clin Periodontol. 2005; 32: 1096-1107.         [ Links ]

17. Xajigeorgiou C, Skellari D, Slini T, Baka A, Konstantinidis A. Clinical and microbiological effects of different antimicrobials on generalized aggressive periodontitis. J Clin Periodontol. 2006; 33: 254-264.         [ Links ]

18. Buchmann R, Nunn ME, Van Dyke TE, Lange DE. Aggressive periodontitis: 5-year follow-up of treatment. J Periodontol. 2002; 73: 675-683.         [ Links ]

19. Sigusch B, Beir M, Klinger G, Pfister W, Glockmann E. A 2-step non surgical procedure and systemic antibiotics in the treatment of rapidly progressive periodontitis. J Periodontol. 2001; 72: 275-283.         [ Links ]

20. Murphy KG, Gunsolley JC. Guided tissue regenration for the treatment of periodontal intrabony and furcation defects. A systematic review. Ann Periodontol. 2003; 8: 266-302.         [ Links ]

21. Reynolds MA, Aichelmann-Reidy ME, Branch-Mays GL, Gunsolley JC. The efficacy of bone replacement grafts in the treatment of periodontal osseous defects. A systematic review. Ann Periodontol. 2003; 8: 227-265.         [ Links ]

22. Anitua E. Plasma rich in growth factors: preliminary results of use in the preparation of future sites for implants. Int J Oral Maxillofac Implants. 1999; 14: 529-535.         [ Links ]

23. Emingil G, Darcan S, Keskinoğlu A, Kütükçüler N, Atilla G. Localized aggressive periodontitis in a patient with type 1 diabetes mellitus: a case report. J Periodontol. 2001; 72: 1265-1270.         [ Links ]

 

LECTURAS RECOMENDADAS

1. Reiner M, Klaus ML, Wilhelm M, Johannes W. A telescopic crown concept for the restoration of partially edentulous patiens with aggressive generalized periodontitis: two case reports. Int J Periodontics Restorative Dent. 2002; 22: 128-137.         [ Links ]

2. Kai PW, Max AL, Jonathan MK. A multidisciplinary approach to the diagnosis and treatment of early-onset periodontitis: a case report. J Periodontol. 2001; 72: 96-106.         [ Links ]

3. John SM, Roselyn C, Lawrence CP. Complications associated with diabetes mellitus after guided tissue regeneration: a case report revisited. Compendiuem. 2002; 23 (12): 1135-1145.         [ Links ]

4. Debora CR, Mario T, Arthur BN, Sergio LS, Marcio FM. Effect of non-surgical periodontal therapy on glycemic control in patients with type 2 diabetes mellitus. J Periodontol. 2003; 74: 1361-1367.         [ Links ]

5. Goerge WT, Brian AB, Mark PB, Robert JG, Marc SW et al. Severa periodontitis and risk for poor glycemic control in patients with non-insulin-dependent diabetes mellitus. J Periodontol. 1996; 67: 1085-1093.         [ Links ]

Mailing address:
María del Carmen López Buendía
E-mail: cdmclopezb@hotmail.com

 

Note

This article can be read in its full version in the following page: http://www.medigraphic.com/facultadodontologiaunam

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