Abstract
D-dimer molecules are formed by the degradation of cross-linked fibrin during the process of fibrinolysis. The formation of D-dimer requires the activity of activated factor XIII (factor XIIIa), plasmin, and thrombin. To assess the awareness about D-dimer assay among dental students. A cross-sectional study was done among 100 dental practitioners through an online survey. The survey consisted of 10 semiclosed prevalidated and reliable questionnaires based on the knowledge, attitude, and practice of the dentists on D-dimer assay. Descriptive and inferential statistics were performed to report the responses of the participants. Most participants did not know what a D-dimer assay is (55%). Forty-six percent of participants responded that the D-dimer assay is used to rule out serious blood clots. Fifty-four percent of the participants responded that fibrin D-dimers are formed when fibrin strands are formed. The current study shows that the knowledge about D-dimer assay is more in CRRI than in participants of junior year of study. Thus, more rigorous educational programs should be initiated to further enrich the knowledge among dental students.
Keywords: Awareness, D-dimer, dental students, innovation
INTRODUCTION
Cross-linked fibrin is broken down into D-dimer molecules during fibrinolysis. Three enzymes are required to make D-dimers: activated factor XIII, plasmin, and thrombin.[1] The coagulation system's thrombin transforms soluble fibrinogen into fibrin monomers, which kicks off the process.[2] Noncovalent connections within the protein are created by the thrombin breakdown of peptides from the N-terminal region, resulting in allosteric alterations.[3] Fibrin is reinforced by interactions with factor XIII, which cross-links the D domains of the nearing fibrin monomers after thrombin activation. A D-dimer molecule is formed when plasmin digests the fibrin clot.[2]
D-dimer measurements are widely conducted with a variety of quantitative and qualitative cutoffs using central laboratory and point-of-care testing.[4] Because D-dimer molecules are formed only when thrombin is created and cross-linked fibrin is broken down, their presence implies intravascular coagulation.[5] Thus, D-dimer levels are taken as an indicator of thrombotic and thrombolytic activity, as well as a worldwide marker of blood coagulation and fibrinolytic system activation.[6]
In various clinical settings, the presence or lack of the D-dimer molecules has a range of effects. Deep-vein thrombosis (DVT), pulmonary embolism (PE), aortic dissection, and disseminated intravascular coagulation (DIC) require D-dimer testing for current triage and diagnosis.[7] D-dimer testing is most useful when the risk of thromboembolism is less, with a negative result surely ruling out thrombosis and a positive result indicating thrombosis.
Since the 1980s, the number of PubMed articles evaluating the use of the D-dimer test results in the diagnosis of clotting diseases has continuously increased. This study combines D-dimer with clinical data as part of a diagnosis, such as determining the duration of anticoagulant therapy and ruling out venous thromboembolism (VTE). Despite the large amount of data, the therapeutic value and importance of many of the findings are still being debated. Several efforts are undertaken to increase the use of the D-dimer test in various medical conditions and integrate it with other laboratory and clinical test results.
Our team has substantial research and knowledge, which has resulted in high-quality publications.[8,9,10,11,12,13,14,15,16,17] The study's goal was to see how well dentistry students knew about the D-dimer assay.
MATERIALS AND METHODS
This is a cross-sectional study done among 100 dental practitioners through an online survey. The survey consisted of 10 semiclosed prevalidated and reliable questionnaires based on the knowledge, attitude, and practice of the dentists on D-dimer assay. The ethical approval of the current study was obtained from the institutional ethical board (IHEC/SDC/PROSTHO/21/044). The consent of the participants has been obtained after explaining the need for the study. Prior approval to carry out the study has been obtained from the international research committee of the author's university. The pros of the study were that it was done through an online survey and was less time-consuming compared to manual methods or entering the responses of the participants. The cons of the survey were the limited geographical area in which data were collected and analyzed using SPSS software version 23.0 (IBM Corp, IBM SPSS Statistics for Windows, Armonk, NY). Descriptive and inferential analyses were performed to report the responses of the participants.
RESULTS
The current study equal number of students for first year to CRRI. It shows that most participants did not know what a D-dimer assay is (55%) [Figure 1]. Most participants in the study thought that the other name of the D-dimer assay was fibrin D-dimer and fibrin degeneration fragment (41%). Most participants knew that the D-dimer assay was a “plasma protein test” (55%) [Figure 2] and is used to rule out serious blood clots (46%) [Figure 3]. Most participants responded that fibrin D-dimers are formed when fibrin strands are formed (54%) and that the elevated level of D-dimer indicates the active formation of blood clots (51%) [Figure 4]. The participants were also aware that the normal level of D-dimer was <0.50 (47%) [Figure 5]. The participants responded that D-dimer is expressed as Fibrinogen Equivalent Units (FEU) (57%) [Figure 6]. It is evident from the association graph that the knowledge about D-dimer is more in senior participants than in juniors (21%) [Figure 7].
Figure 1.

Do you know about D-dimer assay?
Figure 2.

What is D-dimer assay used for?
Figure 3.

What is D-dimer assay used for?
Figure 4.

What does elevated level of D-dimer indicate?
Figure 5.

What is the normal level of D-dimer?
Figure 6.

What causes the increase in D-dimer?
Figure 7.

Correlation between the year of study and the knowledge about D-dimer assay
Figure 1 represents the number of participants who were aware of what a D-dimer assay is. Blue represents response “yes” and green represents response “no.” It is evident that most participants did not know what a D-dimer assay is (55%).
Figure 2 represents the question: what is D-dimer assay used for? Blue represents response “blood tests” and green represents response “plasma protein test.” It is evident that most participants answered “plasma protein test” (55%).
Figure 3 represents the question: What is D-dimer assay used for? Blue represents response “to rule out serious blood clots,” green represents response “to rule out liver diseases,” and brown represents response “to rule out pulmonary embolism.” It is evident that most participants responded that D-dimer assay is used to rule out serious blood clots (46%)
Figure 4 represents the question: What does elevated level of D-dimer indicate? Blue indicates the response “active formation of blood clots” and green represents the response “degeneration of blood clots.” It is evident that most participants responded that elevated level D-dimer indicates the active formation of blood clots (51%).
Figure 5 represents the question: What is the normal level of D-dimer? Blue represents <0.50, green represents 0.60, and brown represents 0.70. It is evident that most participants responded that the normal level of D-dimer <0.50 (47%).
Figure 6 represents the question: What causes the increase in D-dimer? Blue represents clotting problems, green represents pregnancy, and brown represents the response “both.” It is evident that most participants responded to clotting problems (51%).
Figure 7 represents the year of study correlated with knowledge of students about D-dimer assay. Blue represents the response “yes” and green represents the response “no.” The X-axis indicates the year of study and the Y-axis represents the number of responses of students. Participants responded that the D-dimer is expressed as FEU (57%). It is evident that the knowledge about D-dimer is more in senior participants than in juniors (21%).
DISCUSSION
The current study shows the knowledge about D-dimer assay among dental students.[18] The study reveals that the knowledge about D-dimer assay is more in CRRI than in participants in junior year. This result is in correlation with an article written by Favresse et al., who in his study revealed that senior dental practitioners had the most knowledge about D-dimer assay and its uses in clinical practice.[19] There were no studies done on assessing the knowledge about D-dimer assay among dental students.[20]
When a clot dissolves in the human body, one of the protein fragments generated is D-dimer. It is usually undetected or only noticeable at an extremely low level unless the body is creating and breaking down the clots.[21] D-dimer is a blood test that tests for it. When a clinician suspects that the symptoms are caused by anything other than DVT or a PE, the D-dimer test can help. It's a painless and rapid method to rule out irregular or excessive clotting as the source of the issue. However, if the danger of PE is substantial, as determined by a clinical evaluation, it should not be used.
A D-dimer result that is normal or “negative” (below a certain cutoff level) indicates that the person being tested is free of an acute disease or sickness that causes aberrant clot creation and breakdown.[22] A negative D-dimer, according to most doctors, is most valid and advantageous when performed on those who are at risk of thrombosis.[23,24,25,26]
High amounts of fibrin breakdown products could be indicated by a positive D-dimer test.[27] It indicates that a large blood clot (thrombus) has developed and broken down somewhere in the body, but it does not say where or why. VTE or DIC could be the cause of increased levels of D-dimer levels.[28]
CONCLUSION
The current study shows that the knowledge about D-dimer assay is more in CRRI than in participants of junior year of study. Thus, more rigorous educational programs should be initiated to further enrich the knowledge among dental students.
Financial support and sponsorship
The present study is funded by the
Saveetha Institute of Medical and Technical Sciences
Saveetha Dental College and Hospitals
Saveetha University.
Conflicts of interest
There are no conflicts of interest.
Acknowledgment
The authors acknowledge Saveetha University for all the help and support.
REFERENCES
- 1.Ginsberg JS, Wells PS, Kearon C, Anderson D, Crowther M, Weitz JI, et al. Sensitivity and specificity of a rapid whole-blood assay for D-dimer in the diagnosis of pulmonary embolism. Ann Intern Med. 1998;129:1006–11. doi: 10.7326/0003-4819-129-12-199812150-00003. [DOI] [PubMed] [Google Scholar]
- 2.Keeling DM, Wright M, Baker P, Sackett D. D-dimer for the exclusion of venous thromboembolism: Comparison of a new automated latex particle immunoassay (MDA D-dimer) with an established enzyme-linked fluorescent assay (VIDAS D-dimer) Clin Lab Haematol. 1999;21:359–62. doi: 10.1046/j.1365-2257.1999.00248.x. [DOI] [PubMed] [Google Scholar]
- 3.Perrier A, Desmarais S, Goehring C, de Moerloose P, Morabia A, Unger PF, et al. D-dimer testing for suspected pulmonary embolism in outpatients. Am J Respir Crit Care Med. 1997;156:492–6. doi: 10.1164/ajrccm.156.2.9702032. [DOI] [PubMed] [Google Scholar]
- 4.Harper PL, Theakston E, Ahmed J, Ockelford P. D-dimer concentration increases with age reducing the clinical value of the D-dimer assay in the elderly. Intern Med J. 2007;37:607–13. doi: 10.1111/j.1445-5994.2007.01388.x. [DOI] [PubMed] [Google Scholar]
- 5.D'Angelo A, D'Alessandro G, Tomassini L, Pittet JL, Dupuy G, Crippa L. Evaluation of a new rapid quantitative d-dimer assay in patients with clinically suspected deep vein thrombosis. Thromb Haemost. 1996;75:412–6. [PubMed] [Google Scholar]
- 6.Akutsu K, Sato N, Yamamoto T, Morita N, Takagi H, Fujita N, et al. A rapid bedside D-dimer assay (cardiac D-dimer) for screening of clinically suspected acute aortic dissection. Circ J. 2005;69:397–403. doi: 10.1253/circj.69.397. [DOI] [PubMed] [Google Scholar]
- 7.Johnson ED, Schell JC, Rodgers GM. The D-dimer assay. Am J Hematol. 2019;94:833–9. doi: 10.1002/ajh.25482. [DOI] [PubMed] [Google Scholar]
- 8.Ponnanna AA, Maiti S, Rai N, Jessy P. Three-dimensional-Printed Malo Bridge: Digital Fixed Prosthesis for the Partially Edentulous Maxilla. Contemp Clin Dent. 2021;12:451–3. doi: 10.4103/ccd.ccd_456_20. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Maiti S, Aparna J, Jessy P. Polyether ether ketone –As an alternative biomaterial for Metal Richmond crown-3-dimensional finite element analysis. J Conserv Dent. 2021;24:553. doi: 10.4103/jcd.jcd_638_20. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Merchant A, Ganapathy DM, Maiti S. Effectiveness of local and topical anesthesia during gingival retraction. Braz Dent Sci. 2022;25:e2591. [Google Scholar]
- 11.Kasabwala H, Maiti S, Ashok V, Sashank K. Data on dental bite materials with stability and displacement under load. Bioinformation. 2020;16:1145–51. doi: 10.6026/973206300161145. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Agarwal S, Maiti S, Ashok V. Correlation of soft tissue biotype with pink aesthetic score in single full veneer crown. Bioinformation. 2020;16:1139–44. doi: 10.6026/973206300161139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Neha N, Maiti S, Jessy P. Adhesion of microflora and the role of denitrifies in colour stability on provisional crowns: An in-vitro study. Int J Dentistry Oral Sci. 2021;8:3805–9. [Google Scholar]
- 14.Sharmila R, Maiti S, Jessy P. Comparative analysis of abrasion resistance in relation to different temporary acrylic crown material using toothbrush simulator-an in vitro study. Int J Dent Oral Sci. 2021;8:2153–7. [Google Scholar]
- 15.Merchant A, Maiti S, Ashok V, Ganapathy DM. Comparative analysis of different impression techniques in relation to single tooth impression. Bioinformation. 2020;16:1105–10. doi: 10.6026/973206300161105. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Agarwal S, Ashok V, Maiti S. Open- or closed-tray impression technique in implant prosthesis: A dentist's perspective. J Long Term Eff Med Implants. 2020;30:193–8. doi: 10.1615/JLongTermEffMedImplants.2020035933. [DOI] [PubMed] [Google Scholar]
- 17.Rupawat D, Maiti S, Nallaswamy D, Sivaswamy V. Aesthetic outcome of implants in the anterior zone after socket preservation and conventional implant placement: A retrospective study. J Long Term Eff Med Implants. 2020;30:233–9. doi: 10.1615/JLongTermEffMedImplants.2020035942. [DOI] [PubMed] [Google Scholar]
- 18.Heidari A. Spectroscopy and Quantum Mechanics of the Helium Dimer (He2+), Neon Dimer (Ne2+), Argon Dimer (Ar2+), Krypton Dimer (Kr2+), Xenon Dimer (Xe2+), Radon Dimer (Rn2+) and Ununoctium Dimer (Uuo2+) Molecular Cations. Chem Sci J. 2016;7(2):e112. [Google Scholar]
- 19.Favresse J, Lippi G, Roy PM, Chatelain B, Jacqmin H, Ten Cate H, et al. D-dimer: Preanalytical, analytical, postanalytical variables, and clinical applications. Crit Rev Clin Lab Sci. 2018;55:548–77. doi: 10.1080/10408363.2018.1529734. [DOI] [PubMed] [Google Scholar]
- 20.Wells PS, Anderson DR, Rodger M, Forgie M, Kearon C, Dreyer J, et al. Evaluation of D-dimer in the diagnosis of suspected deep-vein thrombosis. N Engl J Med. 2003;349:1227–35. doi: 10.1056/NEJMoa023153. [DOI] [PubMed] [Google Scholar]
- 21.Palareti G, Cosmi B, Legnani C, Tosetto A, Brusi C, Iorio A, et al. D-dimer testing to determine the duration of anticoagulation therapy. N Engl J Med. 2006;355:1780–9. doi: 10.1056/NEJMoa054444. [DOI] [PubMed] [Google Scholar]
- 22.Stein PD, Hull RD, Patel KC, Olson RE, Ghali WA, Brant R, et al. D-dimer for the exclusion of acute venous thrombosis and pulmonary embolism: A systematic review. Ann Intern Med. 2004;140:589–602. doi: 10.7326/0003-4819-140-8-200404200-00005. [DOI] [PubMed] [Google Scholar]
- 23.Zhao Q, Yang Y, He SW, Wang XT, Liu C. Risk factors for intussusception in children with Henoch-Schönlein purpura: A case-control study. World J Clin Cases. 2021;9:6244–53. doi: 10.12998/wjcc.v9.i22.6244. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Li J, Zhou K, Duan H, Yue P, Zheng X, Liu L, et al. Value of D-dimer in predicting various clinical outcomes following community-acquired pneumonia: A network meta-analysis. PLoS One. 2022;17:e0263215. doi: 10.1371/journal.pone.0263215. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Kearon C, de Wit K, Parpia S, Schulman S, Spencer FA, Sharma S, et al. Diagnosis of deep vein thrombosis with D-dimer adjusted to clinical probability: Prospective diagnostic management study. BMJ. 2022:e067378. [Google Scholar]
- 26.Auditeau C, Khider L, Planquette B, Sanchez O, Smadja DM, Gendron N. D-dimer testing in clinical practice in the era of COVID-19. Res Pract Thromb Haemost. 2022;6:e12730. doi: 10.1002/rth2.12730. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Tripodi A. D-dimer testing in laboratory practice. Clin Chem. 2011;57:1256–62. doi: 10.1373/clinchem.2011.166249. [DOI] [PubMed] [Google Scholar]
- 28.Kavak S, Yildirim MS, Altındag R, Mertsoy Y, Alakus MF, Guleken MD, et al. Correlation of neuroimaging findings with clinical presentation and laboratory data in patients with COVID-19: A single-center study. Biomed Res Int 2021. 2021:2013371. doi: 10.1155/2021/2013371. [DOI] [PMC free article] [PubMed] [Google Scholar]
