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International Journal of Dentistry and Oral Science (IJDOS)  /  IJDOS-2377-8075-08-8089

Neuropathic Pain Management in a Tertiary Care Oral Medicine Unit


Abhinaya LM1, Muthukrishnan Arvind2*, Deepika Rajendran3

1 Department of Oral Medicine and Radiology and Special Care Dentistry, Saveetha Dental College and Hospital, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai 600077, Tamil Nadu, India.
2 Professor and Head, Department of Oral Medicine and Radiology and Special Care Dentistry, Saveetha Dental College and Hospital, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai 600077, Tamil Nadu, India.
3 Senior Lecturer, Department of Oral Medicine and Radiology and Special Care Dentistry, Saveetha Dental College and Hospital, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai 600077, Tamil Nadu, India.


*Corresponding Author

Muthukrishnan Arvind,
Professor and Head, Department of Oral Medicine and Radiology and Special Care Dentistry, Saveetha Dental College and Hospital, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai 600077, Tamil Nadu, India.
Tel: 9444303303
E-mail: arvindm@saveetha.com

Received: July 30, 2021; Accepted: August 11, 2021; Published: August 18, 2021

Citation:Abhinaya LM, Muthukrishnan Arvind, Deepika Rajendran. Neuropathic Pain Management in a Tertiary Care Oral Medicine Unit. Int J Dentistry Oral Sci. 2021;8(8):4010-4015. doi: dx.doi.org/10.19070/2377-8075-21000819

Copyright: JMuthukrishnan Arvind©2021. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.



Abstract

Neuropathic pain is initiated by a primary lesion or dysfunction of the nervous system and can be triggered by local trauma or systemic disorders. Neuropathic pain has a complex presentation which is often a diagnostic challenge and requires a multidisciplinary approach in management. Neuropathic pain prevalence is estimated between 1 and 10%, with few studies reporting that neuropathic components can be found in 35% of all painful syndromes. Our aim of the study was to evaluate the most effective treatment modality in management of neuropathic pain. Retrospective analysis was done at the Department of Oral Medicine and Radiology of Saveetha University hospital from June 2019 - March 2020. A total of 32 patients who were diagnosed clinically as Trigeminal neuralgia (TN) and Post herpetic neuralgia (PHN) cases were included in the study. Out of the 32 patients, females (56.2%) were predominant than males (43.7%).Majority of the study patients age group were 60-70 years (37.5%) followed by 50-60 years (31.25%).The study cases consisted of about 96.8% of TN followed by 3.1% of PHN cases. The left trigeminal nerve (53.13%) was more commonly affected when compared to the right trigeminal (46.88%).The branches of the trigeminal nerve affected were higher in V3 (62.5%) and V2 (18.75%). The common medical management of TN involved Carbamazepine (56.25%), combination of Carbamazepine, Gabapentin and Methylcobalamin (28.13%).Only three patients had undergone surgical management for TN (3.13%). Comparison of medical management in the study group using VAS pain scores was done. Neuropathic pain requires a proper evidence based management of pain either medically or surgically. Our study has shown a significant reduction in pain in patients under medical treatment. Clinicians hence must use a systematic approach in management of neuropathic pain with regular follow up.



1.Keywords
2.Introduction
3.Conclusion
4.References


Keywords

Neuropathic Pain; Post Herpetic Neuralgia; Trigeminal Neuralgia; Vas Pain Scale.


Introduction

Neuropathic pain is defined as pain arising as a direct consequence of a lesion or a disease affecting the somatosensory system- The international association for the study of pain (IASP) special interest group on neuropathic pain [22]. Neuropathic pain possesses a significant challenge to diagnosticians due to the complexity involved and managing the condition appropriately[49]. Neuropathic pain is frequently seen with other conditions like diabetes [20], carpal tunnel syndrome, Guillain-Barre syndrome, cancer [23, 58]multiple sclerosis and kidney disorders [48]. Neuropathic pain presents as a chronic pain condition often impacting the quality of life in patients suffering from it. Neuropathic pain is classified into a number of clinical entities, the most common are Trigeminal neuralgia, Glossopharyngeal neuralgia, Post herpetic neuropathies and Burning mouth syndrome.

Trigeminal neuralgia is an excruciating short lasting, unilateral facial pain [37] that may be spontaneous or triggered by gentle [47], innocuous stimuli and separated by pain free intervals of varying duration [19]. Diagnostic criteria recognize two subsets of TN: a classical(previously idiopathic or primary) type and a symptomatic(secondary) TN by the International Headache Society (IHS) [14]. Classical TN may be related to neurovascular compression but may be unrelated to recognizable pathology whereas symptomatic TN that is related to a variety of symptoms and pathologies such as trauma, CNS tumors and systemic disease [19]. Unrecognized [7] by classification is Atypical TN cases (30%) that present with most but not all diagnostic criteria and are often refractory to treatment [26, 41, 51]. Post herpetic neuralgia is a complication of acute herpes zoster (HZ) or shingles. Acute HZ is a reactivation of latent varicella virus infection [54] and may occur decades after primary infection [43]. Trigeminal and cervical nerves are affected in 8% to 28% and 13% to 23% of acute herpes zoster infection cases, respectively [42].

Management of TN includes non-surgical [46] and surgical management. In standard practice, the first line of treatment [4] is carbamazepine, which relieves most of the symptoms followed by other drugs such as oxcarbazepine, phenytoin, baclofen, lamotrigine, gabapentin and sodium valproate [1]. When medication [25] no longer provide relief, surgical management plays a role. Various surgical techniques used for management include percutaneous radiofrequency thermal rhizotomy, physical compression, trigeminal ganglion balloon decompression, botulinum injections, gamma-knife radiosurgery and cryosurgery. All these techniques are aimed at relieving the nerve compression. Research has indicated that there is no influence of age, sex ethnicity or side of face on the management therapy of TN [9].

Management of PHN include tricyclic antidepressants, gabapentin, pregabalin, opioid and topical[8] lidocaine patches as the first line drugs which was proposed by the American Academy of Neurology evidence based guidelines. Therefore, an effective evidence based management with prior sequential clinical examination and accurate diagnosis [31] are essential for the proper management for neuropathic pain. Previously our team has a rich experience in working on various research projects across multiple discipline [15-40]. Now the growing trend in this area motivated us to pursue this project.

Aim of the study was to evaluate the most effective treatment modality in management of neuropathic pain.


Materials and Methods

A retrospective study was conducted in the Department of Oral Medicine of Saveetha University hospital from June 2019 to March 2020. The study was approved by the scientific review board (SRB) and institutional ethical committee (Approval number SDC/SIHEC/2020/DIASDATA /0619-0320). The study consisted of two reviewers - one primary researcher and one department faculty who reviewed the study patients who were diagnosed with Trigeminal neuralgia and Post herpetic neuralgia cases after cross verifying the patient's medical records and clinical photographs.

The retrieved data was then formulated on a excel sheet then later transferred to SPSS software. IBM SPSS 20 was used in the study for statistical analysis. The qualitative variables in the study were sex and age of the patients. The quantitative variables were VAS scores (1-10) which was grouped into Mild(1-4);Moderate (4-7) and Severe (7-10).

Frequency distribution tests and descriptive analysis was done using chi-square tests in SPSS IBM20.


Results & Discussion

In this study a total of 32 patients were included who were diagnosed under Trigeminal neuralgia (TN), and Post herpetic neuralgia (PHN) categories. These included 18 female patients (56.2%) and 14 male patients (43.7%) [Graph 1].

The age of the patients were grouped and frequency distribution of patients were higher in the age group of 60-70 years(37.5%) followed by 40-50 years (31.25%) and 50-60 years (31.25%) [Graph 2].

The study cases consisted of about 96.8% of Trigeminal neuralgia patients (TN) followed by 3.1% of Post herpetic neuralgia cases [Graph 3].

Frequency distribution of the commonly affected side by the trigeminal nerve in the study population was the left side (53.13%) and right side of the face (46.87%)[Graph 4].

The branches of the trigeminal nerve affected were higher in V3 (62.5%) , V2 (18.75%) followed by V2, V3 (15.63%) and V1, V3 (3.13%) [Graph 5].

The common medical management of trigeminal neuralgia involved Carbamazepine (56.25%), combination of Carbamazepine, Gabapentin and Methylcobalamin (28.13%) and Gabapentin and Methylcobalamin (15.63%)[Graph 6].

Only three patients had undergone surgical management for trigeminal neuralgia (3.13%) using cryosurgery, peripheral neurectomy and combination of both [Graph 7].

Descriptive analysis was done using the chi-square test with a p value (p<0.05).

Cross tabulation between pretreatment VAS pain score was statistically not significant (p>0.05) [Graph 8] but there was a significant correlation seen in VAS score following post medical management (p<0.05) [Graph 9].

The International Association for the study of pain (IASP) defines pain as an unpleasant sensory and emotional experience associated with actual or potential tissue damage or described in terms of such damage. Comparison of nociceptive pain and neuropathic pain, neuropathic pain is persistent for longer duration, not responsive to pain [5] medications, often debilitating and difficult to treat. Neuropathic pain was commonly seen in females and in the 60-70 years age group which was similar to the study done by Korczeniewska et al., [17], Siqueira et al., [44]whose mean age was 62.5 years whereas a study done by Bangash et al., [3] showed the mean age to be 54 years.

According to Veerapaneni et al., [53]Trigeminal Neuralgia, was one of the most commonly observed type of neuropathic pain which is similar to our study.The most commonly presented side of pain was left side in our study which was contradicting to the studies done by Bangash et al., [3] who had reported right side being the commonly affected in his study from 2011. Bangash et al had also reported that the commonly affected branch of the trigeminal nerve was the mandibular branch, maxillary and combination of both maxillary and mandibular branch being affected which was similar to our study where 62.5% of cases were affected by the mandibular branch, 18.75% by maxillary and 15.63% were affected by both maxillary and mandibular branch. Post herpetic neuralgia is a neuropathic pain syndrome which is characterized by pain that persists for months to years after resolution of the herpes zoster infection. Management of PHN is prevention using the zoster vaccine and in the later stages through antiviral medication and subsequent pain management.

According to the European Federation of Neurological Societies and the Quality Standards Subcommittee of the American Academy of Neurology, the first line of drugs is Carbamazepine (56.25%) which is similar to the drug management provided to our patients in the study. Study done by Zakrewska et al., [59] showed that carbamazepine, carbamazepine with gabapentin proved effective which was in concordance to our study. Singh et al., [43]study revealed that PHN are treated commonly using the first line of drugs such as carbamazepine and lidocaine patches which was in concordance to our study.

There were very limited data on studies who have compared the VAS scores[24] to that of the management given for Trigeminal neuralgia which is the foreground of our study. The most commonly used surgical management was peripheral neurectomy followed by cryosurgery which was in concordance to our study. Our study though had a significant correlation between medical management and VAS score, Salama et al., [38] study showed poor response with pharmacotherapy and patients experienced drug intolerance. A study done by Turton et al., [50]revealed that there was an ineffectiveness in symptom reduction under medical management and underwent surgical management through microvascular decompression. The drawbacks of our study were that of limited sample size, with shorter period of follow up duration and only VAS pain scale was assessed and the future scope lies in a analysing more patients, initiate multicentric study with proper drug regimen and standardization, monitoring of the adverse effects and attempt usage of alternative drugs such as Cannabis for neuropathic pain management. Our institution is passionate about high quality evidence based research and has excelled in various fields [32-39]. We hope this study adds to this rich legacy.



GRAPH 1: This graph depicts the frequency distribution of gender in the study population. X-axis depicts the gender of patients and Y-axis depicts the number of patients in the study population. The number of female participants were 18 (56.25%) and 14 male participants in the study (43.75%).



GRAPH 2: This graph depicts frequency distribution of patients in different age groups. X-axis depicts the age groups among the study population and Y-axis depicts the number of patients. There were 12 patients in the age group of 60-70 years(37.5%) followed by 10 patients in each 40-50 years (31.25%) and 50-60 years (31.25%).



GRAPH 3: This graph represents the clinical types of neuropathic pain seen in the study population. X-axis depicts the type of neuropathic pain-Trigeminal and Post herpetic neuralgia and Y-axis depicts the number of patients in the study population.31 patients from the study population had Trigeminal neuralgia (96.88%) and one patient with post herpetic neuralgia (3.13%).



GRAPH 4: This graph depicts the side affected by the trigeminal nerve. X-axis depicts the side affected and Y-axis depicts the number of patients.17 patients (53.13%) were affected by the left trigeminal nerve followed by 15 patients (46.88%) affected by left trigeminal nerve.



GRAPH 5: This graph depicts the branches of the trigeminal nerve affected in the study population. X-axis depicts the different branches involved and Y-axis depicts the number of patients. The branches of the trigeminal nerve affected were higher in V3 (62.5%) in 20 patients, V2 (18.75%) in 6 patients, V2,V3 (15.63%) in 5 patients and V1,V3 (3.13%) in one patient.



GRAPH 6: This graph represents the medical management of trigeminal neuralgia cases. X-axis depicts the varied drugs prescribed and Y-axis depicts the number of patients in the study population. 16 patients were prescribed on Carbamazepine (56.25%), 9 patients on combination of Carbamazepine, Gabapentin and Methylcobalamin (28.13%) and 5 patients on Gabapentin and Methylcobalamin (15.63%).



GRAPH 7: This graph depicts the surgical management of trigeminal neuralgia cases. X-axis depicts the varied surgical modalities and Y-axis depicts the number of patients in the study population. Only three patients had undergone surgical management for trigeminal neuralgia (3.13%) using cryosurgery, peripheral neurectomy and combination of both.



GRAPH 8: Bar chart comparing the pretreatment VAS pain score assessment for medical management of neuropathic pain. X-axis depicts the different medications used for neuropathic pain and Y-axis depicts the percentage of cases. Pretreatment VAS scores are graded as Mild (pink); moderate (blue) and severe (green). In the Carbamazepine group, VAS varied from mild to severe. The pretreatment VAS score was moderate in the other 2 groups, Gabapentin + Methylcobalamin (20.8%) and Gabapentin+Methylcobalamin Carbamazepine (25.0%).The chi square analysis [chi-square-3.692;df-4;p- .449(p>0.05)] is statistically not significant. There was no statistical significance on comparison of pretreatment VAS score with different medications used for management of neuropathic pain.



Graph 9 : Bar chart comparing the post treatment VAS pain score assessment for medical management of neuropathic pain. X-axis depicts the different medications used for neuropathic pain and Y-axis depicts the percentage of cases. Post treatment , no patients were in the severe VAS category. In the Carbamazepine group all patients from severe and moderate VAS in pretreatment improved and presented with mild VAS ( 66.7%). The post treatment VAS score varied from moderate to mild in the other 2 groups, Gabapentin + Methylcobalamin and Gabapentin+Methylcobalamin Carbamazepine.The chi square analysis [chi-square-3.562;df-2;p-.016 (p<0.05)] is statistically significant. Carbamazepine medication shows a statistically significant decrease in the VAS score levels when compared to that of the other groups.


Conclusion

Our study results show that there was a significant reduction in the pain symptoms in patients treated with Carbamazepine as the first line of drug for medical management which is a positive outcome. There were only three studies which had undergone surgical management post ineffectiveness under drug therapy. This presents as a strong evidence that maximum number of patients can be treated under medications and have a significant reduction in pain. Only the cases which are proven ineffective under anticonvulsants, relapse cases or patients under medications for a longer duration and have not shown significant reduction in pain can be advised with surgical management. Hence, proper diagnosis followed by relevant medications and follow up can be sufficient in management of majority of neuropathic pain cases.


References

    [1]. Suwal P. ‘General Systemic Evaluation of Prosthodontic Patients: A Literature Review’, 2013;13(2):90–94.
    [2]. Pihlstrom BL, Michalowicz BS, Johnson NW. Periodontal diseases. Lancet. 2005 Nov 19;366(9499):1809-20.
    [3]. Mootha A, Malaiappan S, Jayakumar ND, Varghese SS, Toby Thomas J. The Effect of Periodontitis on Expression of Interleukin-21: A Systematic Review. Int J Inflam. 2016;2016:3507503.Pubmed PMID: 26998377.
    [4]. Varghese SS, Thomas H, Jayakumar ND, Sankari M, Lakshmanan R. Estimation of salivary tumor necrosis factor-alpha in chronic and aggressive periodontitis patients. Contemp Clin Dent. 2015 Sep;6(Suppl 1):S152-6. Pubmed PMID: 26604566.
    [5]. Ramesh A, Varghese SS, Jayakumar ND, Malaiappan S. Chronic obstructive pulmonary disease and periodontitis–unwinding their linking mechanisms. J. Oral Biosci. 2016 Feb 1;58(1):23-6.
    [6]. Priyanka S, Kaarthikeyan G, Nadathur JD, Mohanraj A, Kavarthapu A. Detection of cytomegalovirus, Epstein-Barr virus, and Torque Teno virus in subgingival and atheromatous plaques of cardiac patients with chronic periodontitis. J Indian Soc Periodontol. 2017 Nov-Dec;21(6):456-460.Pubmed PMID: 29551863.
    [7]. Foz AM, Artese HP, Horliana AC, Pannuti CM, Romito GA. Occlusal adjustment associated with periodontal therapy--a systematic review. J Dent. 2012 Dec;40(12):1025-35.Pubmed PMID: 22982113.
    [8]. Herrera D, Roldán S, González I, Sanz M. The periodontal abscess (I). Clinical and microbiological findings. J Clin Periodontol. 2000 Jun;27(6):387- 94.
    [9]. Khalid W, Vargheese SS, Lakshmanan R, Sankari M, Jayakumar ND. Role of endothelin-1 in periodontal diseases: A structured review. Indian J Dent Res. 2016 May-Jun;27(3):323-33.Pubmed PMID: 27411664.
    [10]. Khalid W, Varghese SS, Sankari M, Jayakumar ND. Comparison of Serum Levels of Endothelin-1 in Chronic Periodontitis Patients Before and After Treatment. J Clin Diagn Res. 2017 Apr;11(4):ZC78-ZC81.Pubmed PMID: 28571268.
    [11]. Avinash K, Malaippan S, Dooraiswamy JN. Methods of Isolation and Characterization of Stem Cells from Different Regions of Oral Cavity Using Markers: A Systematic Review. Int J Stem Cells. 2017 May 30;10(1):12-20. Pubmed PMID: 28531913.
    [12]. Ramamurthy JA, Mg V. Comparison of effect of Hiora mouthwash versus Chlorhexidine mouthwash in gingivitis patients: A clinical trial. Asian J Pharm Clin Res. 2018 Jul 7;11(7):84-8.
    [13]. Nyman SR, Lang NP. Tooth mobility and the biological rationale for splinting teeth. Periodontol 2000. 1994 Feb;4(1):15-22.
    [14]. Nyman S, Lindhe J. Persistent tooth hypermobility following completion of periodontal treatment. J Clin Periodontol. 1976 May;3(2):81-93.Pubmed PMID: 1064597.
    [15]. Mühlemann HR. Tooth Mobility: The Measuring Method. Initial and Secondary Tooth Mobility. J Periodontol. 1954 Jan;25(1):22–9.
    [16]. Schulte W, d'Hoedt B, Lukas D, Maunz M, Steppeler M. Periotest for measuring periodontal characteristics--correlation with periodontal bone loss. J Periodontal Res. 1992 May;27(3):184-90.Pubmed PMID: 1608031.
    [17]. Castellini P, Scalise L, Tomasini EP. Teeth mobility measurement: a laser vibrometry approach. J Clin Laser Med Surg. 1998 Oct;16(5):269-72.Pubmed PMID: 9893508.
    [18]. Goellner M, Berthold C, Holst S, Wichmann M, Schmitt J. Correlations between photogrammetric measurements of tooth mobility and the Periotest method. Acta Odontol Scand. 2012 Jan;70(1):27-35.Pubmed PMID: 21504267. [19]. Mühlemann HR. 10 years of tooth-mobility measurements. J. Periodontol. 1960 Apr;31(2):110-22. [20]. Persson R. Assessment of tooth mobility using small loads. II. Effect of oral hygiene procedures. J Clin Periodontol. 1980 Dec;7(6):506-15.Pubmed PMID: 7012187.
    [21]. Persson R. Assessment of tooth mobility using small loads. III. Effect of periodontal treatment including a gingivectomy procedure. J Clin Periodontol. 1981 Feb;8(1):4-11.Pubmed PMID: 6941976.
    [22]. Serio FG. Clinical rationale for tooth stabilization and splinting. Dent Clin North Am. 1999 Jan 1;43(1):1-6.
    [23]. Forabosco A, Grandi T, Cotti B. The importance of splinting of teeth in the therapy of periodontitis. Minerva Stomatol. 2006 Mar;55(3):87-97.Pubmed PMID: 16575381.
    [24]. Thamaraiselvan M, Elavarasu S, Thangakumaran S, Gadagi JS, Arthie T. Comparative clinical evaluation of coronally advanced flap with or without platelet rich fibrin membrane in the treatment of isolated gingival recession. J Indian Soc Periodontol. 2015 Jan;19(1):66.
    [25]. Ravi S, Malaiappan S, Varghese S, Jayakumar ND, Prakasam G. Additive Effect of Plasma Rich in Growth Factors With Guided Tissue Regeneration in Treatment of Intrabony Defects in Patients With Chronic Periodontitis: A Split-Mouth Randomized Controlled Clinical Trial. J Periodontol. 2017 Sep;88(9):839-845.Pubmed PMID: 28474968.
    [26]. Panda S, Jayakumar ND, Sankari M, Varghese SS, Kumar DS. Platelet rich fibrin and xenograft in treatment of intrabony defect. Contemp Clin Dent. 2014 Oct;5(4):550.
    [27]. Ramesh A, Ravi S, Kaarthikeyan G. Comprehensive rehabilitation using dental implants in generalized aggressive periodontitis. J Indian Soc Periodontol. 2017 Mar;21(2):160.
    [28]. Kavarthapu A, Thamaraiselvan M. Assessing the variation in course and position of inferior alveolar nerve among south Indian population: A cone beam computed tomographic study. Indian J Dent Res. 2018 Jul- Aug;29(4):405-409.Pubmed PMID: 30127186.
    [29]. Ramesh A, Vellayappan R, Ravi S, Gurumoorthy K. Esthetic lip repositioning: A cosmetic approach for correction of gummy smile - A case series. J Indian Soc Periodontol. 2019 May-Jun;23(3):290-294.Pubmed PMID: 31143013.
    [30]. Ramesh A, Varghese SS, Doraiswamy JN, Malaiappan S. Herbs as an antioxidant arsenal for periodontal diseases. J Intercult Ethnopharmacol. 2016 Jan 27;5(1):92-6.Pubmed PMID: 27069730.
    [31]. Soares PB, Fernandes Neto AJ, Magalhães D, Versluis A, Soares CJ. Effect of bone loss simulation and periodontal splinting on bone strain: Periodontal splints and bone strain. Arch Oral Biol. 2011 Nov;56(11):1373-81.Pubmed PMID: 21550587.
    [32]. Jain AR. Prevalence of partial edentulousness and treatment needs in rural population of South India. World J. Dent. 2017 Jun;8(3):213-7.
    [33]. Varghese SS, Ramesh A, Veeraiyan DN. Blended Module-Based Teaching in Biostatistics and Research Methodology: A Retrospective Study with Postgraduate Dental Students. J Dent Educ. 2019 Apr;83(4):445-450.Pubmed PMID: 30745352.
    [34]. Ashok V, Ganapathy D. A geometrical method to classify face forms. J Oral Biol Craniofac Res. 2019 Jul 1;9(3):232-5.
    [35]. Padavala S, Sukumaran G. Molar incisor hypomineralization and its prevalence. Contemp. Clin. Dent. 2018 Sep;9(Suppl 2):S246-50.
    [36]. Ke Y, Al Aboody MS, Alturaiki W, Alsagaby SA, Alfaiz FA, Veeraraghavan VP, et al. Photosynthesized gold nanoparticles from Catharanthus roseus induces caspase-mediated apoptosis in cervical cancer cells (HeLa). Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):1938-1946.Pubmed PMID: 31099261.
    [37]. Ezhilarasan D. Oxidative stress is bane in chronic liver diseases: Clinical and experimental perspective. Arab J Gastroenterol. 2018 Jun;19(2):56-64.Pubmed PMID: 29853428. [38]. Krishnan RP, Ramani P, Sherlin HJ, Sukumaran G, Ramasubramanian A, Jayaraj G, et al. Surgical Specimen Handover from Operation Theater to Laboratory: A Survey. Ann Maxillofac Surg. 2018 Jul-Dec;8(2):234-238. Pubmed PMID: 30693238.
    [39]. Ezhilarasan D, Sokal E, Najimi M. Hepatic fibrosis: It is time to go with hepatic stellate cell-specific therapeutic targets. Hepatobiliary Pancreat Dis Int. 2018 Jun;17(3):192-197.Pubmed PMID: 29709350.
    [40]. Pandian KS, Krishnan S, Kumar SA. Angular photogrammetric analysis of the soft-tissue facial profile of Indian adults. Indian J. Dent. Res. 2018 Mar 1;29(2):137-43.
    [41]. Ramamurthy JA, Mg V. Comparison of effect of Hiora mouthwash versus Chlorhexidine mouthwash in gingivitis patients: A clinical trial. Asian J Pharm Clin Res. 2018 Jul 7;11(7):84-8.
    [42]. Gupta P, Ariga P, Deogade SC. Effect of Monopoly-coating Agent on the Surface Roughness of a Tissue Conditioner Subjected to Cleansing and Disinfection: A Contact Profilometric In vitro Study. Contemp Clin Dent. 2018 Jun;9(Suppl 1):S122-S126.Pubmed PMID: 29962776.
    [43]. Vikram NR, Prabhakar R, Kumar SA, Karthikeyan MK, Saravanan R. Ball Headed Mini Implant. J Clin Diagn Res. 2017 Jan;11(1):ZL02-3.
    [44]. Paramasivam A, Vijayashree Priyadharsini J, Raghunandhakumar S. N6- adenosine methylation (m6A): a promising new molecular target in hypertension and cardiovascular diseases. Hypertens Res. 2020 Feb;43(2):153- 154.Pubmed PMID: 31578458.
    [45]. Palati S, Ramani P, Shrelin HJ, Sukumaran G, Ramasubramanian A, Don KR, et al. Knowledge, Attitude and practice survey on the perspective of oral lesions and dental health in geriatric patients residing in old age homes. Indian J Dent Res. 2020 Jan-Feb;31(1):22-25.Pubmed PMID: 32246676.
    [46]. Samuel SR, Acharya S, Rao JC. School Interventions-based Prevention of Early-Childhood Caries among 3-5-year-old children from very low socioeconomic status: Two-year randomized trial. J Public Health Dent. 2020 Jan;80(1):51-60.Pubmed PMID: 31710096.
    [47]. Ebeleseder KA, Glockner K, Pertl C, Städtler P. Splints made of wire and composite: an investigation of lateral tooth mobility in vivo. Endod Dent Traumatol. 1995 Dec;11(6):288-93.Pubmed PMID: 8617165.
    [48]. Kumbuloglu O, Saracoglu A, Ozcan M. Pilot study of unidirectional E-glass fibre-reinforced composite resin splints: up to 4.5-year clinical follow-up. J Dent. 2011 Dec;39(12):871-7.Pubmed PMID: 22001066.
    [49]. Sekhar LC, Koganti VP, Shankar BR, Gopinath A. A comparative study of temporary splints: bonded polyethylene fiber reinforcement ribbon and stainless steel wire + composite resin splint in the treatment of chronic periodontitis. J Contemp Dent Pract. 2011 Sep 1;12(5):343-9.Pubmed PMID: 22269194.
    [50]. Bhawna G. Burden of smoked and smokeless tobacco consumption in India - results from the Global adult Tobacco Survey India (GATS-India)- 2009-2010. Asian Pac J Cancer Prev. 2013;14(5):3323-9.Pubmed PMID: 23803124.
    [51]. Kinane DF, Chestnutt IG. Smoking and periodontal disease. Crit Rev Oral Biol Med. 2000 Jul;11(3):356-65.
    [52]. Sobouti F, Rakhshan V, Saravi MG, Zamanian A, Shariati M. Two-year survival analysis of twisted wire fixed retainer versus spiral wire and fiberreinforced composite retainers: a preliminary explorative single-blind randomized clinical trial. Korean J Orthod. 2016 Mar;46(2):104-10.Pubmed PMID: 27019825.
    [53]. Akcali A, Gümüs P, Özcan M. Clinical comparison of fiber-reinforced composite and stainless steel wire for splinting periodontally treated mobile teeth. Braz. Dent. Sci. 2014 Aug 25;17(3):39-49.
    [54]. Vijayashree Priyadharsini J. In silico validation of the non-antibiotic drugs acetaminophen and ibuprofen as antibacterial agents against red complex pathogens. J Periodontol. 2019 Dec;90(12):1441-1448.Pubmed PMID: 31257588.
    [55]. Pc J, Marimuthu T, Devadoss P, Kumar SM. Prevalence and measurement of anterior loop of the mandibular canal using CBCT: A cross sectional study. Clin Implant Dent Relat Res. 2018 Apr 6;20(4):531-4.
    [56]. Ramesh A, Varghese S, Jayakumar ND, Malaiappan S. Comparative estimation of sulfiredoxin levels between chronic periodontitis and healthy patients - A case-control study. J Periodontol. 2018 Oct;89(10):1241-1248.Pubmed PMID: 30044495.
    [57]. Ramadurai N, Gurunathan D, Samuel AV, Subramanian E, Rodrigues SJ. Effectiveness of 2% Articaine as an anesthetic agent in children: randomized controlled trial. Clin Oral Investig. 2019 Sep;23(9):3543-50.
    [58]. Sridharan G, Ramani P, Patankar S, Vijayaraghavan R. Evaluation of salivary metabolomics in oral leukoplakia and oral squamous cell carcinoma. J Oral Pathol Med. 2019 Apr;48(4):299-306.
    [59]. Ezhilarasan D, Apoorva VS, Ashok Vardhan N. Syzygium cumini extract induced reactive oxygen species-mediated apoptosis in human oral squamous carcinoma cells. J Oral Pathol Med. 2019 Feb;48(2):115-121.Pubmed PMID: 30451321.
    [60]. Mathew MG, Samuel SR, Soni AJ, Roopa KB. Evaluation of adhesion of Streptococcus mutans, plaque accumulation on zirconia and stainless steel crowns, and surrounding gingival inflammation in primary molars: randomized controlled trial. Clin Oral Investig. 2020 Sep;24(9):1-6.Pubmed PMID: 31955271.
    [61]. Samuel SR. Can 5-year-olds sensibly self-report the impact of developmental enamel defects on their quality of life? Int J Paediatr Dent. 2021 Mar;31(2):285-286.Pubmed PMID: 32416620.
    [62]. R H, Ramani P, Ramanathan A, R JM, S G, Ramasubramanian A, et al. CYP2 C9 polymorphism among patients with oral squamous cell carcinoma and its role in altering the metabolism of benzo[a]pyrene. Oral Surg Oral Med Oral Pathol Oral Radiol. 2020 Sep;130(3):306-312.Pubmed PMID: 32773350.
    [63]. Chandrasekar R, Chandrasekhar S, Sundari KKS, Ravi P. Development and validation of a formula for objective assessment of cervical vertebral bone age. Prog Orthod. 2020 Oct 12;21(1):38.Pubmed PMID: 33043408.
    [64]. Vijayashree Priyadharsini J, Smiline Girija AS, Paramasivam A. In silico analysis of virulence genes in an emerging dental pathogen A. baumannii and related species. Arch Oral Biol. 2018 Oct;94:93-98.Pubmed PMID: 30015217.

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