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International Journal of Trend in Scientific Research and Development (IJTSRD)
Volume 5 Issue 3, March-April 2021 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470
@ IJTSRD | Unique Paper ID – IJTSRD37981 | Volume – 5 | Issue – 3 | March-April 2021 Page 832
Chairside Diagnosis of Periodontal Diseases: A Review
Dr. Sumeet Khanna, Dr. Smarth Khanna, Dr. Parul Goel
PG Student, Department of Periodontology and Implantology,
Desh Bhagat Dental College and Hospital, Gobindgarh, Punjab, India
ABSTRACT
A good clinical diagnosis has always been the need of the hour. Proper
diagnosis is essential for better treatment and planning of the diseases.
Customary clinical estimations utilized for periodontal findingareregularlyof
restricted convenience as they are pointers of past periodontal illnessinstead
of present disease action. Subsequently, there is a requirement for creating
novel demonstrative kits that can identify dynamic diseases, anticipatefuture
illness crisis or movement and assess reaction to periodontal treatment, and
treatment encouragement in periodontal patients. In this futuristic era, there
has been a tremendous amount of research in the field of diagnostic tools that
can be utilized by a dental practitioners and even periodontists in their dayto
day practice. Distinctive chair side diagnostic kits will be discussed in this
paper which will be useful for appropriate diagnosis, assessing the disease
anticipation and proper treatment planning.
KEYWORD: CHAIR SIDE TESTS, DIAGNOSIS, PERIODONTAL DISEASES, SALIVA
How to cite this paper: Dr. Sumeet
Khanna | Dr. Smarth Khanna | Dr. Parul
Goel "Chairside Diagnosis of Periodontal
Diseases: A Review"
Published in
International Journal
of Trend in Scientific
Research and
Development(ijtsrd),
ISSN: 2456-6470,
Volume-5 | Issue-3,
April 2021, pp.832-835, URL:
www.ijtsrd.com/papers/ijtsrd37981.pdf
Copyright © 2021 by author (s) and
International Journal ofTrendinScientific
Research and Development Journal. This
is an Open Access article distributed
under the terms of
the Creative
CommonsAttribution
License (CC BY 4.0)
(http://creativecommons.org/licenses/by/4.0)
INTRODUCTION
Periodontitis is a setofprovocativeinfectionsinfluencing the
periodontium, i.e.,thetissuesthatencompassanduphold the
teeth. Periodontitis incorporate progressive loss of the
alveolar bone, and at whatever point left untreated, can
incite the loosening and subsequent loss of teeth.
Periodontitis is caused bythemicroorganismsthatadhereto
and grow on the tooth's surfaces, accessible an over-
aggressiveimmune response againstthesemicroorganisms.1
An analysis of periodontitis is set up by investigatingthesoft
gingival tissues around the teeth with a probe and by
assessing the patient's X-ray films, to decide the amount of
bone loss and the extend of periodontitis around the teeth.2
Diagnosis is the identification of any condition, disease, or
disorder due to any methodical investigation of the history,
assessment of the signsorsymptoms,andexaminationof the
study results. Successful prognosisispreposterouswithouta
viable diagnosis.3 Similarly, a "Periodontal Diagnosis" is a
significant label that a clinician ties on the periodontal
disease state of the patient, capturing all his previous
involvement in the condition. The grouping of signsandside
effects, alongside a detailed history is evoked, reported and
deciphered to reach at a determination. Frequently an exact
analysis is, the absolute first solid advance step towards the
arrangement and execution of an individualized treatment
plan, contributing essentially towards the achievement of
the treatment.4
It is moderately simple to recognize anatomical damage,
caused by advanced stage of periodontitiswithsymptomatic
guides. On the other hand, incipient disease identification
fills in as a test in any event, for the most experienced
clinician. Accentuation on early discovery fills in as a drive
for dealing with the illness with negligibly intrusive and
financial helpful modalities.5 Consequently, there is a
requirement for creating novel indicative units that can
identify dynamic infection, anticipate future illness crisis or
movement and assess reaction to periodontal treatment,
treatment encouraging administration of periodontal
patient. The accessible chair side indicative units are
intended to quantify microbiological, immunologic and
hereditary constituent in oral analytic liquids such as saliva
or gingival crevicular fluid, which can be an indicative of the
diseases.6
The main aim behind the emergence of different diagnostic
tests is that the previous active dynamic disease is analyzed,
the less intrusive, the less time devouring and therefore the
less expensive the required treatment and the better long
haul visualization for patients with damaging disease.7
IDEAL CHARACTERISTICS OF A DIAGNOSTIC KIT8
1. Quantitative.
2. Exceptionally delicate strategy fit for investigating a
single periodontal site in wellbeing just as disease.
3. Reproducible and amendable for chair side use.
4. Exceptionally explicit.
5. Easy to perform and Versatile.
6. Rapid, one or two stage technique.
7. Non-obtrusive and Affordable.
IJTSRD37981
International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD37981 | Volume – 5 | Issue – 3 | March-April 2021 Page 833
Different specialized challenges in conventional techniques
from sample taking to dispersion, cultivation,
characterization, and identification of isolates and issues
related with sufficient investigation of microbiologic
information makes regular symptomatic techniques time
consuming and cumbersome.1 In this context chairside
periodontal diagnostic kits provides a quick reports.
These diagnostic kits can be characterized as Biochemical
kits, Genetic kits and Microbiological kits.
BIOCHEMICAL KITS
Biochemical test unitsutilizedinperiodonticsinvestigate the
gingival crevicular liquid (GCF). Since this liquid is retrieved
from periodontal tissues, assessing its constituents, like
inflammatory mediators, host derived enzymes and
extracellular matrix components may give early indications
of changes. Kits included are:
Perio-Check (Ac Tech): has 88% sensitivity and 61%
specificity. It is the most rapid chair side test for neutral
proteases like collagenases in GCF. The degrees of these
proteins in GCF have been noted to increment with the
advancement of gingival disease as well as development of
established periodontitis. Interproximal areas can't be
inspected because of the risk of saliva contamination.9
PerioGard TM: depends on the estimation of protein level,
aspartate aminotransferase (AST) in GCF. The test is
intended to be positive at >800 μIU of AST activity and
negative at values less than 800 μIU. One of the major
disadvantages of periogard is that it cannot distinguish
between sites with severe inflammation but with no
attachment loss from sites with attachment loss.10
PocketWatchTM: method is use to analyze AST at the
chairside. It is conceivable to distinguish between dynamic
and latent sites. AST action dictated by PocketWatchTM
provides not only an index of cell death but the degree of the
destructive pockets.11
Prognos-Stik (Dentsply): This framework recognizes the
presence of serine proteinase elastase in GCF sample.10
Perio2000: framework is planned sothatitconsolidates the
highlights of a periodontal test with
the measurement of probing depths, to evaluate bleeding on
probing and recognition of unpredictable sulfurmixesin the
periodontal pocket. Sulfide sensor component is employed
with traditional techniques within the evaluation of
periodontal diseases in patients.12
Dip Stick Test: The MMP-8 test stick depends on the
immune-chromatography rule that utilizes two monoclonal
antibodies explicit for various epitopes of MMP-8. The test
stick results can be distinguished in 5 minutes. Theantibody
identifies the two neutrophils and non-PMN-type MMP-8
isoforms.13
TOPAS (Toxicity Prescreening Assay): distinguishes the
indirect presence of microorganisms by two markers of
gingival contamination: bacterial toxins and bacterial
proteins. This test can be related with the severity of
inflammation and with the advancement of destructive
process making the contrast between an active and a latent
periodontal disease.14
Oral Fluid Nano Sensor Test (OFNASET): is a miniature
electromechanical framework based on electrochemical
detection platform that is capableofreal time,ultrasensitive,
ultra specific multiplex recognition of salivary protein and
RNA biomarkers. OFNASET is utilizedforthepurposeofcare
multiplex recognition of salivary biomarkers for oral
malignant growth. It analyses saliva for the presence of four
salivary mRNA biomarkers (SAT, ODZ, IL-8, and IL-1β) and
two salivary proteomic biomarkers(thioredoxinandIL-8).12
Integrated Micro fluidic Platform for Oral Diagnostics
(IMPOD): A clinical point of care diagnostic test empowers
fast evaluation of an oral diseasebiomarkersinhumansaliva
by utilizing a solid dispensable cartridgeintendedtowork in
a conservative diagnostic instrument. Quickly (< 10 min)
measures MMP-8 in saliva from healthy and periodontally
diseased subjects.15
Electronic Taste Chips (ETC): They are synthetically
sensitized bead microreactors inside the lab-on-a-chip
framework and were applied forestimationofCRPandother
biomarkers of inflammation in salivation. With this
procedure it was conceivable to quantitate the distinction in
CRP levels between healthy and patients with periodontal
infections and can simultaneously screen several
biomarkers.15
GENETIC TEST KITS
Different gene polymorphisms are viewed as risk factors for
the inception or movement of periodontal infection.
Kornman et a (1997), found a relationship between the
polymorphism in gene encoding for interleukin-1α and
interleukin-1β and increased severity of periodontitis.
Although genetic identification is a difficult procedure and
requires an experiencedhand,howeversomechairsideunits
are now accessible for its recognition.16
MyPerioID: test utilizes saliva to decide patient's genetic
susceptibility to periodontal disease and which patients are
at higher risk of more serious periodontal diseases.
PST Genetic Susceptibility Test: It assessestheconcurrent
event of allele 2 at the IL-1A +4845 and 1B +3954 loci that
identify individual’s predisposition for the expression of
inflammation and risk for periodontal diseases.5
MICROBIOLOGICAL TEST KITS
Counting and Identification of the microflora in periodontal
pocket have been a significant piece of exploration
endeavors for a long time. It is assumed that atleast of 300
particular bacterial species can repress the periodontal
pocket. A large number of these have not been recognized.
The microbiological tests can possibly uphold the finding of
different types of periodontal infection, to fill in as pointers
of disease commencement and progression andtofigure out
which periodontal sites are at higher risk for dynamic
annihilation. These tests mostly focused on spirochetes, Aa,
Pg and Pi.
Evalusite (Kodak): It is a novel membrane immunoassay
monetarily accessible in Europe and Canada for the
Chairside identification of 3 periodontal microbes. It
includes linkage between the antigen and a layer bound
neutralizer to frame an immunocomplex that is uncovered
through a calorimetric response.Membraneboundantibody
response in the well explicit to A.actinomycetemcomitans,
P.gingivalisandP.intermedia respondswith plaquesample.17
OMNIGENE (DMDx): A. actinomycetemcomitanscloned test
and P gingivalis entire genomic test involve the basis of the
commercial DMDx identification strategy. For P. gingivalis,
the DNA test examine can give a false negative data.
International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD37981 | Volume – 5 | Issue – 3 | March-April 2021 Page 834
Steenbergen et al foundthe DMDxidentificationtechniqueto
have 96% affectability and 86% particularity for spiked lab
examples of A. actinomycetemcomitans and 60%
affectability and 82% particularity for lab examples of
P.gingivalis.8 However, in clinical specimens a reverse
scenario is seen.17
PERIOSCAN: with 99% sensitivity and 55% specificity is a
chair side diagnostic measure that recognizes an
accumulation of periodontal microbe’s B. forsythus, P.
gingivalis, T. denticola and certain Capnocytophaga species
that produce trypsin like enzyme by using BANA. It cannot
recognize the presence of different microorganisms that
don't produce trypsin like catalyst. The outcomes are
subjective and depend upon the administrator'sappraisal at
the calorimetric end point. The particular microscopic
organisms that are answerableforchemical creationcan't be
determined.This BANA test is extremelydelicate,identifying
even minute amounts of microbes. The test can also be
utilized for evaluation of oral halitosis, to recognize the
presence of two BANA positive species on the tongue
surface: Stomatococcus mucinlagenous and Rothia
dentocariosa.9
IAI PADO TEST 4.5: With the PADO RNA probe test unit,
four periodontal microbes can be recognized: A.
actinomycetemcomitans, P. gingivalis, T. forsythia also, T.
denticola. This test utilizes oligonucleotide probes
corresponding to moderated pieces of the 16S rRNA quality
that encodes the rRNA, which structures a subunit of the
bacterial ribosome. The discovery frequencies discovered
showed a low affectability of the PadoTest 4.5 technique
contrasted with thecheckerboardstrategy.ThePadoTest4.5
appears to disparage the quantity of positive sites
recommended by a high number of false negatives.18
My PerioPath: utilizes a saliva test to recognize thesortand
centralization of the particular microbes that cause
periodontal disease. This test requires the transportation of
saliva tests to a research center for results.12
DNA probes: these are very specific and are utilized to
decide phenotypic marker and has an extraordinary
specificity and sensitivity. These are single stranded pieces
of nucleic acid, marked with a particular tracer that will
hydrogen bond with integral single stranded pieceofDNAor
RNA under the appropriate conditions of pH, temperature
and notorious quality. DNA tests deal with the guideline of
the DNA base sequencing. The reciprocally of DNA is in view
of the hydrogen holding between the bases adenine and
thymine, and guanine and cytosine, separately.19
Microprobe Corporation: It is planned as an in-office
nucleic acid test measure for the semi quantitative location
of periodontal microbes. The bacterial cells in subject’s
plaque samples are lysed by warming within the sight of
detergent. The extracted DNA is then positioned in to the
first well of multi-well cassette and afterward positioned
into a machine with a programmable mechanical arm which
shows computerized current bacterial load.19
CONCLUSION
In any branch of medical field, the success of treatment
entirely depends upon the accuracyofdiagnosis.Recently,in
periodontology chronic periodontitis cases can be managed
accurately by using existing diagnostic methodologies, in
spite of the fact that it is obviously more alluring to have the
option to analyze "dynamic infection" when it happens, as
opposed to months after the fact. Chair side diagnostic test
kits offer fast, reproducible method of diagnosis and the
outcomes can be utilized for persistent inspiration too. They
are helpful particularly in making out the active sites and
observing patients post treatment for assessing the reaction
to treatment and disease recurrence. Incorporating new
salivary indicative techniques to clinical practiceiscritical to
help dental experts in making basic wellbeing related
choices for patients.
REFERENCES:
[1] Newman MG, Takei H, Klokkevold PR, and Carranza
FA. Carranza's clinical periodontology.Elsevierhealth
sciences; 2011 Feb 14.
[2] Savage A, Kenneth A., Moles R., Needleman, and Ian.
"A systematic review of definitions of periodontitis
and methods that have been used to identify this
disease". J Clin Periodontol 2009; 36 (6): 458–467.
[3] King LS. What is a diagnosis? JAMA. 1967 Nov 20;
202(8):714-7.
[4] Armitage G C. Periodontal diagnosisandclassification
of periodontal disease. Periodontol 2000 2004;34:9-
21.
[5] Pajnigara NG, Kolte AP, Kolte RA, and Pajnigara NG.
Chair side diagnostic kits in periodontics.
International dental journal of student’s research.
2016 Apr; 4:25-31.
[6] Chepuri T, Gooty JR, Durvasala S, and Palaparthi R.
Chair side diagnostic test kits in periodontics. Indian
Journal of Dental Advancements. 2015 Jan 1;7(1):41-
6.
[7] Kinane DF. Regulators of tissue destruction and
homeostasis as diagnostic aids in periodontology.
Periodontol 2000; 24:215–25.
[8] Chapple IL. Periodontal diagnosis and treatment-
where does the future lie? Periodontol 2009;51:9-24.
[9] Hemmings KW, Griffiths GS, and Bulman JS.Detection
of neutral protease (Periocheck)andBANAhydrolase
(Perioscan) compared with traditional clinical
methods of diagnosis and monitoring of chronic
inflammatory periodontal disease. J Clin Periodontol
1997; 24:110-114.
[10] Persson GR, Alves MEAF, Chambers DA, Clark WB,
Cohen R. Crawford JM, et al A multicetiterclinieal trial
of PerioGardTM in distinguishing between diseased
and healthy periodontal sites. Study design,
methodology and therapeutic outcome. J Clin
Periodontol 1995; 22:794-803.
[11] Shimada K, Mizuno T, Ohshio K, Kamaga M, Murai S,
and Ito K. Analysis of aspartate aminotransferase in
gingival crevicular fluid assessed by using
PocketWatchTM: a longitudinal study with initial
therapy. J Clin Periodontol 2000; 27:819–223.
[12] Gupta M, Nirola A, and Bhardwaj SJ. Advances in
clinical diagnosis in Periodontics. Indian Journal of
Dental Sciences 2012; 4(4):114-118.
[13] Mantyla P, Stenman M, Kinane DF, Tikanoja S, Luoto
H, Salo T, et al. Gingival crevicular fluid collagenase-2
(MMP-8) test stick for chair-side monitoring of
periodontitis. J Periodontal Res2003;38(4):436–439.
International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD37981 | Volume – 5 | Issue – 3 | March-April 2021 Page 835
[14] Pucau CG, Dumitriu A, and Dumitriu HT. Biochemical
and enzymatic diagnosis aids in periodontal disease.
OHDMBSC 2005; 4:19-25.
[15] Herr AE, Hatch AV, and Giannobile WV. Integrated
microfluidic platform for oral diagnostics. Ann N Y
Acad Sci 2007; 1098: 362–374.
[16] Kornman K, and Crane A. The interleukin-1 genotype
as a severity factor in adult periodontal disease. J Clin
Periodontal 1997;24;72-77.
[17] Thomas Biju et al. "Chairside Diagnostic test kits in
Periodontics".JIDA 2007; 1(10)
[18] Leonhardt A, Carlen A, and Dahlen G. Detection of
Periodontal Markers in Chronic Periodontitis. Open
Dent J 2011; 5:110-115.
[19] Singh V, P Anuradha, S Sahana, Narayan M, Agarwal S,
and Singh S. DNA Probes: Newer Diagnostic Aid in
Periodontal Disease. J Adv Med Dent Scie Res
2019;7(2):49-51

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Chairside Diagnosis of Periodontal Diseases A Review

  • 1. International Journal of Trend in Scientific Research and Development (IJTSRD) Volume 5 Issue 3, March-April 2021 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470 @ IJTSRD | Unique Paper ID – IJTSRD37981 | Volume – 5 | Issue – 3 | March-April 2021 Page 832 Chairside Diagnosis of Periodontal Diseases: A Review Dr. Sumeet Khanna, Dr. Smarth Khanna, Dr. Parul Goel PG Student, Department of Periodontology and Implantology, Desh Bhagat Dental College and Hospital, Gobindgarh, Punjab, India ABSTRACT A good clinical diagnosis has always been the need of the hour. Proper diagnosis is essential for better treatment and planning of the diseases. Customary clinical estimations utilized for periodontal findingareregularlyof restricted convenience as they are pointers of past periodontal illnessinstead of present disease action. Subsequently, there is a requirement for creating novel demonstrative kits that can identify dynamic diseases, anticipatefuture illness crisis or movement and assess reaction to periodontal treatment, and treatment encouragement in periodontal patients. In this futuristic era, there has been a tremendous amount of research in the field of diagnostic tools that can be utilized by a dental practitioners and even periodontists in their dayto day practice. Distinctive chair side diagnostic kits will be discussed in this paper which will be useful for appropriate diagnosis, assessing the disease anticipation and proper treatment planning. KEYWORD: CHAIR SIDE TESTS, DIAGNOSIS, PERIODONTAL DISEASES, SALIVA How to cite this paper: Dr. Sumeet Khanna | Dr. Smarth Khanna | Dr. Parul Goel "Chairside Diagnosis of Periodontal Diseases: A Review" Published in International Journal of Trend in Scientific Research and Development(ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-3, April 2021, pp.832-835, URL: www.ijtsrd.com/papers/ijtsrd37981.pdf Copyright © 2021 by author (s) and International Journal ofTrendinScientific Research and Development Journal. This is an Open Access article distributed under the terms of the Creative CommonsAttribution License (CC BY 4.0) (http://creativecommons.org/licenses/by/4.0) INTRODUCTION Periodontitis is a setofprovocativeinfectionsinfluencing the periodontium, i.e.,thetissuesthatencompassanduphold the teeth. Periodontitis incorporate progressive loss of the alveolar bone, and at whatever point left untreated, can incite the loosening and subsequent loss of teeth. Periodontitis is caused bythemicroorganismsthatadhereto and grow on the tooth's surfaces, accessible an over- aggressiveimmune response againstthesemicroorganisms.1 An analysis of periodontitis is set up by investigatingthesoft gingival tissues around the teeth with a probe and by assessing the patient's X-ray films, to decide the amount of bone loss and the extend of periodontitis around the teeth.2 Diagnosis is the identification of any condition, disease, or disorder due to any methodical investigation of the history, assessment of the signsorsymptoms,andexaminationof the study results. Successful prognosisispreposterouswithouta viable diagnosis.3 Similarly, a "Periodontal Diagnosis" is a significant label that a clinician ties on the periodontal disease state of the patient, capturing all his previous involvement in the condition. The grouping of signsandside effects, alongside a detailed history is evoked, reported and deciphered to reach at a determination. Frequently an exact analysis is, the absolute first solid advance step towards the arrangement and execution of an individualized treatment plan, contributing essentially towards the achievement of the treatment.4 It is moderately simple to recognize anatomical damage, caused by advanced stage of periodontitiswithsymptomatic guides. On the other hand, incipient disease identification fills in as a test in any event, for the most experienced clinician. Accentuation on early discovery fills in as a drive for dealing with the illness with negligibly intrusive and financial helpful modalities.5 Consequently, there is a requirement for creating novel indicative units that can identify dynamic infection, anticipate future illness crisis or movement and assess reaction to periodontal treatment, treatment encouraging administration of periodontal patient. The accessible chair side indicative units are intended to quantify microbiological, immunologic and hereditary constituent in oral analytic liquids such as saliva or gingival crevicular fluid, which can be an indicative of the diseases.6 The main aim behind the emergence of different diagnostic tests is that the previous active dynamic disease is analyzed, the less intrusive, the less time devouring and therefore the less expensive the required treatment and the better long haul visualization for patients with damaging disease.7 IDEAL CHARACTERISTICS OF A DIAGNOSTIC KIT8 1. Quantitative. 2. Exceptionally delicate strategy fit for investigating a single periodontal site in wellbeing just as disease. 3. Reproducible and amendable for chair side use. 4. Exceptionally explicit. 5. Easy to perform and Versatile. 6. Rapid, one or two stage technique. 7. Non-obtrusive and Affordable. IJTSRD37981
  • 2. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD37981 | Volume – 5 | Issue – 3 | March-April 2021 Page 833 Different specialized challenges in conventional techniques from sample taking to dispersion, cultivation, characterization, and identification of isolates and issues related with sufficient investigation of microbiologic information makes regular symptomatic techniques time consuming and cumbersome.1 In this context chairside periodontal diagnostic kits provides a quick reports. These diagnostic kits can be characterized as Biochemical kits, Genetic kits and Microbiological kits. BIOCHEMICAL KITS Biochemical test unitsutilizedinperiodonticsinvestigate the gingival crevicular liquid (GCF). Since this liquid is retrieved from periodontal tissues, assessing its constituents, like inflammatory mediators, host derived enzymes and extracellular matrix components may give early indications of changes. Kits included are: Perio-Check (Ac Tech): has 88% sensitivity and 61% specificity. It is the most rapid chair side test for neutral proteases like collagenases in GCF. The degrees of these proteins in GCF have been noted to increment with the advancement of gingival disease as well as development of established periodontitis. Interproximal areas can't be inspected because of the risk of saliva contamination.9 PerioGard TM: depends on the estimation of protein level, aspartate aminotransferase (AST) in GCF. The test is intended to be positive at >800 μIU of AST activity and negative at values less than 800 μIU. One of the major disadvantages of periogard is that it cannot distinguish between sites with severe inflammation but with no attachment loss from sites with attachment loss.10 PocketWatchTM: method is use to analyze AST at the chairside. It is conceivable to distinguish between dynamic and latent sites. AST action dictated by PocketWatchTM provides not only an index of cell death but the degree of the destructive pockets.11 Prognos-Stik (Dentsply): This framework recognizes the presence of serine proteinase elastase in GCF sample.10 Perio2000: framework is planned sothatitconsolidates the highlights of a periodontal test with the measurement of probing depths, to evaluate bleeding on probing and recognition of unpredictable sulfurmixesin the periodontal pocket. Sulfide sensor component is employed with traditional techniques within the evaluation of periodontal diseases in patients.12 Dip Stick Test: The MMP-8 test stick depends on the immune-chromatography rule that utilizes two monoclonal antibodies explicit for various epitopes of MMP-8. The test stick results can be distinguished in 5 minutes. Theantibody identifies the two neutrophils and non-PMN-type MMP-8 isoforms.13 TOPAS (Toxicity Prescreening Assay): distinguishes the indirect presence of microorganisms by two markers of gingival contamination: bacterial toxins and bacterial proteins. This test can be related with the severity of inflammation and with the advancement of destructive process making the contrast between an active and a latent periodontal disease.14 Oral Fluid Nano Sensor Test (OFNASET): is a miniature electromechanical framework based on electrochemical detection platform that is capableofreal time,ultrasensitive, ultra specific multiplex recognition of salivary protein and RNA biomarkers. OFNASET is utilizedforthepurposeofcare multiplex recognition of salivary biomarkers for oral malignant growth. It analyses saliva for the presence of four salivary mRNA biomarkers (SAT, ODZ, IL-8, and IL-1β) and two salivary proteomic biomarkers(thioredoxinandIL-8).12 Integrated Micro fluidic Platform for Oral Diagnostics (IMPOD): A clinical point of care diagnostic test empowers fast evaluation of an oral diseasebiomarkersinhumansaliva by utilizing a solid dispensable cartridgeintendedtowork in a conservative diagnostic instrument. Quickly (< 10 min) measures MMP-8 in saliva from healthy and periodontally diseased subjects.15 Electronic Taste Chips (ETC): They are synthetically sensitized bead microreactors inside the lab-on-a-chip framework and were applied forestimationofCRPandother biomarkers of inflammation in salivation. With this procedure it was conceivable to quantitate the distinction in CRP levels between healthy and patients with periodontal infections and can simultaneously screen several biomarkers.15 GENETIC TEST KITS Different gene polymorphisms are viewed as risk factors for the inception or movement of periodontal infection. Kornman et a (1997), found a relationship between the polymorphism in gene encoding for interleukin-1α and interleukin-1β and increased severity of periodontitis. Although genetic identification is a difficult procedure and requires an experiencedhand,howeversomechairsideunits are now accessible for its recognition.16 MyPerioID: test utilizes saliva to decide patient's genetic susceptibility to periodontal disease and which patients are at higher risk of more serious periodontal diseases. PST Genetic Susceptibility Test: It assessestheconcurrent event of allele 2 at the IL-1A +4845 and 1B +3954 loci that identify individual’s predisposition for the expression of inflammation and risk for periodontal diseases.5 MICROBIOLOGICAL TEST KITS Counting and Identification of the microflora in periodontal pocket have been a significant piece of exploration endeavors for a long time. It is assumed that atleast of 300 particular bacterial species can repress the periodontal pocket. A large number of these have not been recognized. The microbiological tests can possibly uphold the finding of different types of periodontal infection, to fill in as pointers of disease commencement and progression andtofigure out which periodontal sites are at higher risk for dynamic annihilation. These tests mostly focused on spirochetes, Aa, Pg and Pi. Evalusite (Kodak): It is a novel membrane immunoassay monetarily accessible in Europe and Canada for the Chairside identification of 3 periodontal microbes. It includes linkage between the antigen and a layer bound neutralizer to frame an immunocomplex that is uncovered through a calorimetric response.Membraneboundantibody response in the well explicit to A.actinomycetemcomitans, P.gingivalisandP.intermedia respondswith plaquesample.17 OMNIGENE (DMDx): A. actinomycetemcomitanscloned test and P gingivalis entire genomic test involve the basis of the commercial DMDx identification strategy. For P. gingivalis, the DNA test examine can give a false negative data.
  • 3. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD37981 | Volume – 5 | Issue – 3 | March-April 2021 Page 834 Steenbergen et al foundthe DMDxidentificationtechniqueto have 96% affectability and 86% particularity for spiked lab examples of A. actinomycetemcomitans and 60% affectability and 82% particularity for lab examples of P.gingivalis.8 However, in clinical specimens a reverse scenario is seen.17 PERIOSCAN: with 99% sensitivity and 55% specificity is a chair side diagnostic measure that recognizes an accumulation of periodontal microbe’s B. forsythus, P. gingivalis, T. denticola and certain Capnocytophaga species that produce trypsin like enzyme by using BANA. It cannot recognize the presence of different microorganisms that don't produce trypsin like catalyst. The outcomes are subjective and depend upon the administrator'sappraisal at the calorimetric end point. The particular microscopic organisms that are answerableforchemical creationcan't be determined.This BANA test is extremelydelicate,identifying even minute amounts of microbes. The test can also be utilized for evaluation of oral halitosis, to recognize the presence of two BANA positive species on the tongue surface: Stomatococcus mucinlagenous and Rothia dentocariosa.9 IAI PADO TEST 4.5: With the PADO RNA probe test unit, four periodontal microbes can be recognized: A. actinomycetemcomitans, P. gingivalis, T. forsythia also, T. denticola. This test utilizes oligonucleotide probes corresponding to moderated pieces of the 16S rRNA quality that encodes the rRNA, which structures a subunit of the bacterial ribosome. The discovery frequencies discovered showed a low affectability of the PadoTest 4.5 technique contrasted with thecheckerboardstrategy.ThePadoTest4.5 appears to disparage the quantity of positive sites recommended by a high number of false negatives.18 My PerioPath: utilizes a saliva test to recognize thesortand centralization of the particular microbes that cause periodontal disease. This test requires the transportation of saliva tests to a research center for results.12 DNA probes: these are very specific and are utilized to decide phenotypic marker and has an extraordinary specificity and sensitivity. These are single stranded pieces of nucleic acid, marked with a particular tracer that will hydrogen bond with integral single stranded pieceofDNAor RNA under the appropriate conditions of pH, temperature and notorious quality. DNA tests deal with the guideline of the DNA base sequencing. The reciprocally of DNA is in view of the hydrogen holding between the bases adenine and thymine, and guanine and cytosine, separately.19 Microprobe Corporation: It is planned as an in-office nucleic acid test measure for the semi quantitative location of periodontal microbes. The bacterial cells in subject’s plaque samples are lysed by warming within the sight of detergent. The extracted DNA is then positioned in to the first well of multi-well cassette and afterward positioned into a machine with a programmable mechanical arm which shows computerized current bacterial load.19 CONCLUSION In any branch of medical field, the success of treatment entirely depends upon the accuracyofdiagnosis.Recently,in periodontology chronic periodontitis cases can be managed accurately by using existing diagnostic methodologies, in spite of the fact that it is obviously more alluring to have the option to analyze "dynamic infection" when it happens, as opposed to months after the fact. Chair side diagnostic test kits offer fast, reproducible method of diagnosis and the outcomes can be utilized for persistent inspiration too. They are helpful particularly in making out the active sites and observing patients post treatment for assessing the reaction to treatment and disease recurrence. Incorporating new salivary indicative techniques to clinical practiceiscritical to help dental experts in making basic wellbeing related choices for patients. REFERENCES: [1] Newman MG, Takei H, Klokkevold PR, and Carranza FA. Carranza's clinical periodontology.Elsevierhealth sciences; 2011 Feb 14. [2] Savage A, Kenneth A., Moles R., Needleman, and Ian. "A systematic review of definitions of periodontitis and methods that have been used to identify this disease". J Clin Periodontol 2009; 36 (6): 458–467. [3] King LS. What is a diagnosis? JAMA. 1967 Nov 20; 202(8):714-7. [4] Armitage G C. Periodontal diagnosisandclassification of periodontal disease. Periodontol 2000 2004;34:9- 21. [5] Pajnigara NG, Kolte AP, Kolte RA, and Pajnigara NG. Chair side diagnostic kits in periodontics. International dental journal of student’s research. 2016 Apr; 4:25-31. [6] Chepuri T, Gooty JR, Durvasala S, and Palaparthi R. Chair side diagnostic test kits in periodontics. Indian Journal of Dental Advancements. 2015 Jan 1;7(1):41- 6. [7] Kinane DF. Regulators of tissue destruction and homeostasis as diagnostic aids in periodontology. Periodontol 2000; 24:215–25. [8] Chapple IL. Periodontal diagnosis and treatment- where does the future lie? Periodontol 2009;51:9-24. [9] Hemmings KW, Griffiths GS, and Bulman JS.Detection of neutral protease (Periocheck)andBANAhydrolase (Perioscan) compared with traditional clinical methods of diagnosis and monitoring of chronic inflammatory periodontal disease. J Clin Periodontol 1997; 24:110-114. [10] Persson GR, Alves MEAF, Chambers DA, Clark WB, Cohen R. Crawford JM, et al A multicetiterclinieal trial of PerioGardTM in distinguishing between diseased and healthy periodontal sites. Study design, methodology and therapeutic outcome. J Clin Periodontol 1995; 22:794-803. [11] Shimada K, Mizuno T, Ohshio K, Kamaga M, Murai S, and Ito K. Analysis of aspartate aminotransferase in gingival crevicular fluid assessed by using PocketWatchTM: a longitudinal study with initial therapy. J Clin Periodontol 2000; 27:819–223. [12] Gupta M, Nirola A, and Bhardwaj SJ. Advances in clinical diagnosis in Periodontics. Indian Journal of Dental Sciences 2012; 4(4):114-118. [13] Mantyla P, Stenman M, Kinane DF, Tikanoja S, Luoto H, Salo T, et al. Gingival crevicular fluid collagenase-2 (MMP-8) test stick for chair-side monitoring of periodontitis. J Periodontal Res2003;38(4):436–439.
  • 4. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD37981 | Volume – 5 | Issue – 3 | March-April 2021 Page 835 [14] Pucau CG, Dumitriu A, and Dumitriu HT. Biochemical and enzymatic diagnosis aids in periodontal disease. OHDMBSC 2005; 4:19-25. [15] Herr AE, Hatch AV, and Giannobile WV. Integrated microfluidic platform for oral diagnostics. Ann N Y Acad Sci 2007; 1098: 362–374. [16] Kornman K, and Crane A. The interleukin-1 genotype as a severity factor in adult periodontal disease. J Clin Periodontal 1997;24;72-77. [17] Thomas Biju et al. "Chairside Diagnostic test kits in Periodontics".JIDA 2007; 1(10) [18] Leonhardt A, Carlen A, and Dahlen G. Detection of Periodontal Markers in Chronic Periodontitis. Open Dent J 2011; 5:110-115. [19] Singh V, P Anuradha, S Sahana, Narayan M, Agarwal S, and Singh S. DNA Probes: Newer Diagnostic Aid in Periodontal Disease. J Adv Med Dent Scie Res 2019;7(2):49-51