Accepted on 20 Dec 2019
Submitted on 20 Dec 2019
Non-communicable diseases (NCDs) are rising in prevalence globally in line with an increasingly ageing population, refined diets and sedentary lifestyles. NCDs account for 41 million deaths each year, or 71% of all global deaths [40]. Approximately 80% of people over the age of 65 in the USA are affected by one or more NCDs, and 77% exhibit at least two NCDs, creating a significant burden of disease to individuals and to the healthcare economy [13]. The co-morbid presence of two or more NCDs presents a major challenge to the economy, equating to two thirds of all health costs in the USA [14]; however, less than 1% of health expenditure in the USA is focussed on prevention to improve overall health [129].
The greatest global NCD burden arises due to cardiovascular disease (CVD), which is responsible for 17.9 million deaths (one third of total mortality) and 45% of NCD-induced mortality [104]. In Europe, CVD is responsible for 3.9 million deaths (45% of deaths), and whilst CVD mortality rates are reducing, the absolute numbers have increased in the last 25 years due to an increasingly ageing population [135]. Ischaemic heart disease, stroke, hypertension (leading to heart failure), rheumatic heart disease, cardiomyopathy and atrial fibrillation cause over 95% of CVD-related deaths [103].
In this consensus report, the term CVD is used as a general term for atherosclerotic diseases, principally coronary heart disease, cerebrovascular disease and peripheral vascular disease. A number of chronic infectious-inflammatory-immune diseases are associated with significantly higher risks of adverse cardiovascular events, including rheumatoid arthritis, psoriasis, systemic lupus erythematosus and periodontitis [103], consistent with the thesis that chronic elevations in the systemic inflammatory burden are causally related to CVD development and its sequelae. Whilst there is evidence for over 50 gene polymorphisms playing a role in the modulation of atherogenesis [46], effect sizes are small and the major traditional risk factors for CVD remain lifestyle factors, principally tobacco smoking, dyslipidaemia, hypertension and altered glucose metabolism. The latter correlate strongly with diets high in saturated fats, salt and refined sugars and contribute to obesity and type 2 diabetes mellitus, major attributable risk factors for myocardial infarction [50]. The same risk factors account for over 90% of the stroke burden [87], yet all are modifiable through improved lifestyles, including reducing salt, saturated fat and refined carbohydrate intake, exercising, increasing intake of antioxidant micronutrients and regular moderate alcohol consumption [50].
Periodontitis is also an NCD with a high prevalence of 45–50% overall, with the most severe form affecting 11.2% of the world’s population, making it the sixth most common human disease [52]. The Global Burden of Diseases, Injuries, and Risk Factors Study (2017) of Years Lost to Disability (YLD) reported that from 1990 to 2017 oral diseases (mainly periodontitis and caries) contributed the most YLD in age-standardised prevalence rates from 354 diseases and injuries across 195 countries [39]. There is now a significant body of evidence to support independent associations between severe periodontitis and several NCDs, including diabetes [17], cardiovascular disease [128], chronic obstructive pulmonary disease [64] and chronic kidney disease (CKD) [117]. Indeed, severe periodontitis is independently and significantly associated with all-cause and cardiovascular mortality in several different populations [63, 117]. Proposed mechanisms include bacteraemia and the associated systemic inflammatory sequelae, including elevations in C-reactive protein and oxidative stress [113]. In populations with multi-morbidity, for example chronic kidney disease with co-morbid diabetes and periodontitis, periodontitis is associated with significantly reduced survival from all-cause and cardiovascular mortality [117]. It appears, therefore, that periodontitis may be a modifiable non-traditional risk factor for CVD.
In 2012 a joint workshop was held between the European Federation of Periodontology (EFP) and the American Academy of Periodontology to review the literature relating periodontitis and systemic diseases, including CVD. The consensus report was based upon four technical papers that systematically reviewed the evidence for epidemiological associations between periodontitis and incident CVD [28], mechanisms of biological plausibility relating to periodontal bacteria and systemic inflammation [101, 113] and periodontal intervention studies [23]. The workshop concluded there was consistent and strong epidemiological evidence that periodontitis imparts increased risk for future atherosclerotic cardiovascular disease. It also concluded the impact of periodontitis on CVD was biologically plausible, via translocated circulating oral microbiota, which may directly or indirectly induce systemic inflammation that impacts upon the development of atherothrombogenesis, and whilst in vitro, pre-clinical and clinical studies supported the interaction and associated biological mechanisms, intervention trials were not sufficiently adequate to draw further conclusions at that time.
The present workshop was jointly organised by the EFP and the World Heart Federation (WHF) to include global experts in both periodontal and cardiovascular disciplines and was held in Madrid on 18 and 19 February 2019. Four technical reviews updating the evidence base from the 2012 workshop were prepared and supplemented by additional studies discussed at the workshop. The reviews focussed on epidemiological associations [45], mechanistic links [114], results from intervention studies [89] and the potential risk and complications of periodontal therapy in patients undertaking antithrombotic (antiplatelet and anticoagulant) therapy.
While this consensus report focuses predominantly on relevant evidence published since the 2012 workshop, there are biological areas that have subsequently come to prominence, and where the underpinning body of evidence was not covered in the 2013 consensus report; hence, certain pre-2012 manuscripts are referenced to ensure the context of these recent studies is clear.
Furthermore, sections 4.3: What is the effect of statin intake on clinical periodontal outcomes? and section 5: Cardiovascular risks and complications of periodontal therapeutic interventions were not dealt with in the previous workshop; hence, a full appraisal of the scientific evidence was carried out in this consensus meeting.
Finally, following the review of the presented evidence, recommendations for both medical and dental teams, as well as patients and the public, were elaborated.
There is evidence from epidemiological studies that periodontitis patients exhibit significant endothelial dysfunction, measured by flow mediated dilation (FMD), arterial stiffness (e.g., pulse wave velocity – PWV) and a significantly greater thickness of the carotid intima media (cIMT) and elevated arterial calcification scores. There is one imaging study (ATHEROREMO-IVUS study) associating high levels of antibodies against periodontal pathogens and a lower extent of positive atheromatous plaque remodelling [24].
There is robust evidence from epidemiological studies for a positive association between periodontitis and coronary heart disease. A systematic review [28], which was updated in preparation for this workshop, identified a total of six case-control and cohort epidemiological studies, published in the last five years, which demonstrated an increased risk of a first coronary event in patients with clinically diagnosed periodontitis or more severe periodontitis compared to patients without periodontitis or less severe periodontitis. Relative risk estimates vary between studies, depending on population characteristics and periodontitis case definitions. There are two cohort studies reporting an association between periodontitis and higher cardiovascular mortality (due to coronary heart disease and cerebrovascular disease).
There is evidence from epidemiologic studies for a positive association between periodontitis and cerebrovascular disease. A systematic review [28], which was updated in preparation for this workshop, identified a total of three case-control and cohort studies, which demonstrate an increased risk of a first cerebrovascular event in patients with clinically diagnosed periodontitis or more severe periodontitis compared to patients without periodontitis or less severe periodontitis. Relative risk estimates vary between studies, depending on population characteristics and periodontitis case definitions. Furthermore, a recent analysis of data from the Atherosclerosis Risk in Communities (ARIC) study demonstrated an association between periodontal profile class and incident ischemic stroke. In this cohort, patients with periodontitis had more than double the risk of cardioembolic and thrombotic stroke compared to periodontally healthy individuals [115]. In addition, as previously documented, there are two cohort studies reporting an association between periodontitis and higher cardiovascular mortality (due to coronary heart disease and cerebrovascular disease) [28].
There is limited but consistent evidence that individuals with periodontitis have a higher prevalence and incidence of PAD compared to individuals without periodontitis [140]. For cross-sectional data, the most significant evidence comes from two large, population-based studies in the USA (NHANES 1999–2002) and South Korea (KoGES-CAVAS). Both studies found a positive association between the extent of clinical attachment loss (NHANES 1999–2002) and severity of radiographic bone loss (KoGES-CAVAS) with PAD, defined using the Ankle Brachial Index (ABI), with adjusted odd ratios (OR) of 2.2 (95% confidence interval -CI-; [1.2; 2.4]) and 2.0 (95% CI [1.1; 3.9]), respectively [2, 70]. One prospective cohort study, conducted in male veterans in the USA, reported a positive association between periodontitis (measured by severity of radiographic bone loss) and the incidence of PAD over a 25–30 year follow-up period, with an adjusted OR of 2.3 (95% CI [1.3; 3.9]) [77]. There are no studies that have evaluated the association between periodontitis and the incidence of Major Adverse Limb Events (MALE).
Several studies report positive associations between periodontitis and heart failure. There is evidence from a large Asian study using the Taiwanese National Health Insurance Research Database reporting a significantly higher incidence of atrial fibrillation in individuals with periodontal diseases compared to individuals without periodontal diseases (hazard ratio –HR = 1.31, 95% CI [1.25; 1.36]) [18].
There is currently limited scientific evidence that CVD is a risk factor for the onset or progression of periodontitis.
From three studies investigating the association between periodontitis and secondary cardiovascular events, two large studies did not find a significant association [31, 100]; however, a small study (100 subjects) reported a significant association (HR = 2.8, 95% CI [1.2; 6.5]) with recurrent cerebro-vascular events [116].
There is evidence that oral bacterial species can enter the circulation and cause bacteremia, which has been demonstrated following daily life activities (tooth brushing, flossing, chewing or biting an apple), although it has been studied more frequently following professional interventions (tooth polishing, scaling, tooth extraction, surgical extraction of third molars and periodontal probing).
The risk of bacteremia has been associated with periodontal health status in a systematic review, suggesting a higher risk of bacteremia associated with gingival inflammation [127]. A recent randomized clinical trial (RCT) concluded that periodontal therapy (by means of scaling and root planing, SRP) induced bacteremia in both gingivitis and periodontitis patients, but the magnitude and frequency were greater among periodontitis patients [5].
Whilst there are methodological limitations in some of the reported studies, the overall picture supports the contention that bacteremia results from daily life activities and oral interventions, and it is more frequent, of longer duration and involves more virulent bacteria in periodontitis patients.
There is evidence through traces of DNA, RNA or antigens derived from oral bacterial species, mainly periodontal pathogens, that have been identified in atherothrombotic tissues. Studies have attempted to correlate the presence of these bacteria in atherothrombotic tissues with other sample sources (subgingival plaque, serum, etc.) in the same patients, and these suggest that in periodontitis patients there is a higher probability of a positive correlation [3, 73]. At least two studies have demonstrated viable P. gingivalis and A. actinomycetemcomitans in athero-thrombotic tissue when culturing the atheroma samples [56, 98].
Different animal models have been employed to provide evidence that periodontal pathogens can promote atheroma formation. P. gingivalis has been shown to accelerate atherosclerosis in murine models, to induce fatty streaks in the aorta of rabbits and to induce aortic and coronary lesions after bacteremia in normocholesterolaemic pigs (Schenkein & Loos. 2003).
Recently, further evidence has emerged using hyperlipidemic ApoEnull mice after infection with P. gingivalis and also with a polymicrobial experimental infection (P. gingivalis, Treponema denticola, Tannerella forsythia and Fusobacterium nucleatum). A polymicrobial infection was shown to induce aortic toll-like receptor (TLR) and inflammasome signaling, with an enhanced oxidative stress reaction generated within the aortic endothelial cells [20, 131, 132].
There is also in vitro evidence of intracellular entry by periodontal pathogens (P. gingivalis, A. actinomycetemcomitans, etc.) [101]. In vivo and in vitro studies demonstrate the importance of the fimbriae of P. gingivalis to host cell entry and to promote atherothrombotic lesions in experimental models [138]. In vitro experiments have shown certain bacterial strains expressing P. gingivalis hemagglutinin A (HagA) have an increased capability to adhere and enter human coronary artery endothelial cells (HCAEC) [7].
There is evidence of significantly higher levels of C-reactive protein (CRP) in periodontitis patients versus healthy controls and in CVD and periodontitis patients compared with either condition alone. The effect of periodontal therapy has been shown to associate with a significant decrease in CRP levels, along with improvements in surrogate measurements of cardiovascular health [27, 55, 93].
There is evidence of elevated levels of serum interleukin (IL)-6 in periodontitis patients and lower levels of IL-4 and IL-18. The effect of periodontal therapy has shown a significant decrease in the serum levels of IL-6, serum amyloid A and alpha 1 anti-chymotripsin. Peripheral neutrophils from periodontitis patients release excess IL-1β, IL-8, IL-6 and tumour necrosis factor (TNF)-α when stimulated by periodontal pathogens. Periodontal therapy only partially reduces the cytokine hyperreactivity with some evidence of a constitutively elevated response [66].
There is evidence of significantly higher levels of fibrinogen in periodontitis patients versus healthy controls and in CVD and periodontitis patients compared with either condition alone [15]. Periodontal therapy appears to result in a significant decrease in fibrinogen levels [69, 133].
There is evidence from different studies of significantly higher levels of platelet activation markers in periodontitis patients and that these higher levels may be reversed by periodontal therapy [4]. However, there is conflicting evidence that significantly higher levels of plasminogen activator inhibitor (PAI) are found in periodontitis patients (Schenkein & Loos. 2003).
There is evidence that Heat Shock Proteins (HSP) from periodontal pathogens (Porphyromona gingivalis, Tannerella forsythia, Aggregatibacter actinomycetemcomitans and Fusobacterium nucleatum) generate antibodies that can cross-react with human HSPs. These antibodies have been shown to activate cytokine production, as well as monocyte and endothelial cell activation.
Presence of anti-cardiolipin antibodies have been significantly associated in periodontitis patients, which reversed following periodontal therapy. There is some evidence that periodontal pathogens can elicit antibodies that cross-react with cardiolipin (Schenkein & Loos. 2003).
In three out of four population-based studies (Parogene study, NHANES III, DANHES), higher levels of serum immunoglobulin (Ig)G against P. gingivalis were associated with periodontitis patients and cardiovascular disease (acute coronary syndrome, death from cardiovascular disease and cardiovascular disease). The ATHEROREMO-IVUS study failed to demonstrate an association between serum levels of IgG and IgA against P. gingivalis, A. actinomycetemcomitans, T. forsythia and P. intermedia and major adverse cardiac events (MACE) [24]. This is consistent with data from Boillot et al. [11].
There is evidence from systematic reviews that serum total cholesterol levels, low-density lipoproteins (LDL), triglycerides, very low-density lipoproteins (VLDL), oxidized LDL and phospholipase A2 are elevated in periodontitis. High-density lipoprotein (HDL) levels are reduced in periodontitis patients compared with controls (Schenkein & Loos. 2003). These levels are reversed after periodontal therapy [125].
There is strong mechanistic evidence that peripheral blood neutrophils (PBNs) from periodontitis patients produce higher levels of total and extracellular reactive oxygen species (ROS) than healthy controls, under various conditions of priming and stimulation and from unstimulated cells [66, 74]. This hyper-reactivity to stimulation by periodontal bacteria is reduced following successful periodontal therapy to control patient levels, but the unstimulated hyperactivity remains, suggesting constitutive and reactive mechanisms underlie neutrophil hyper-responsiveness in periodontitis [75]. Gene expression data in PBNs supports the functional data [136]. Serum antioxidant levels and those in gingival crevicular fluid (GCF) are reduced in periodontitis patients, reflecting increased ROS activity [16]. This data is supported by a study of endarterectomy samples, which demonstrated evidence for activation of the ROS-generating systems in neutrophils, specifically the presence of myeloperoxidase (MPO), cell-free DNA and DNA-MPO complexes [99].
There is scientific evidence of pleiotropy between periodontitis and cardiovascular diseases [1, 83, 111, 112]. The highly pleiotropic genetic locus CDKN2B-AS1 (chromosome 9, p21.3) associated with coronary artery disease, type 2 diabetes, ischemic stroke and Alzheimer’s disease is also consistently associated with periodontitis [1, 33, 68, 83]. Its function appears to be related to the regulation of gene expression [48]. Interestingly, a pilot study identified that a genetic variant in the CDKN2B-AS1 locus was associated with the extent of elevated levels of C-reactive protein in periodontitis [124].
A conserved non-coding element within CAMTA1 upstream of VAMP3, also first identified as a genetic susceptibility locus for coronary artery disease, was found to be associated with periodontitis [111]. A GWAS suggested the VAMP3 locus was associated with a higher probability of subgingival overgrowth of periodontal pathogens [29].
There is evidence for plasminogen (PLG) as a shared genetic risk factor for coronary artery disease and periodontitis [111].
The fourth pleiotropic locus between coronary artery disease and periodontitis is a haplotype block at the VAMP8 locus [83].
These shared genetic factors suggest a mechanistic link or immunological commonalities between coronary artery disease and periodontitis. The impairment of the regulatory pathways by genetic factors may be a common pathogenic denominator of at least coronary artery disease and periodontitis. There are indications that aberrant inflammatory reactivity, determined by genetic variants in the loci CDKN2B-AS1 (ANRIL), PLG, CAMTA1/VAMP3 and VAMP8 could partially explain the epidemiological link between periodontitis and cardiovascular diseases.
There have been no prospective randomized controlled periodontal intervention studies on primary prevention of cardiovascular diseases (including first ischemic events or cardiovascular death) since the last consensus report [128]. The Group questioned the feasibility of performing adequately powered RCTs in primary prevention at a population level due to important ethical, methodological and financial considerations.
However, consistent observational evidence suggests several oral health interventions, including self-performed oral hygiene habits (toothbrushing) (two studies: [25, 91]), dental prophylaxis (one study: [60]), increased self-reported dental visits (one study: [115]) and periodontal treatment (three studies: [47, 60, 91] produced a reduction in the incidence of ACVD events.
Cross-sectional data of the Scottish Health Surveys from 1995 to 2003 pertaining to 11,869 men and women (mean age of 50 years) was linked to a database of hospital admissions and deaths with follow-up until December 2007 (Information Services Division, Edinburgh) [25]. Participants who brushed less than once a day exhibited the highest incidence of ACVD events (HR = 1.7, 95% CI [1.3; 2.3]) compared with those who brushed twice a day, indicating that self-performed oral hygiene routines may reduce the incidence of ACVD.
A retrospective nationwide, population-based study in Taiwan, including 511,630 participants with periodontitis and 208,713 controls, used the Longitudinal Health Insurance Database 2000 to estimate the incidence rate of ACVD events from 2000 to 2015 [60]. The hazard ratio for acute myocardial infarction was reduced more in the group of periodontitis patients who received dental prophylaxis (HR = 0.90, 95% CI [0.86; 0.95]) than intensive treatment (including gingival curettage, scaling and root planing, and/or periodontal flap operation and/or tooth extraction) (HR = 1.09, 95% CI [1.03; 1.15]). Consistent reductions in the incidence rate of Ischemic Stroke were observed in both the dental prophylaxis (HR = 0.78, 95% CI [0.75; 0.91]) and intensive treatment groups (HR = 0.95, 95% CI [0.91; 0.99]).
A cohort of 8,999 patients with periodontitis who received a complete (non-surgical and if needed surgical) periodontal treatment protocol were followed between 1979 and 2012 [47]. During the study follow-up, poor responders to the periodontal treatment had an increased incidence of ACVD events (incidence rate –IR = 1.28, 95% CI [1.07; 1.53]) compared with good responders, suggesting successful periodontal treatment could reduce the incidence of ACVD events.
In the Atherosclerosis Risk in Communities (ARIC) study, including 6,736 participants followed during 15 years, self-reported regular dental care users had a lower risk for ischemic stroke (HR = 0.77, 95% CI [0.63; 0.94]) compared to episodic care users [115].
A prospective population-based study using data from the National Health Insurance System-National Health Screening Cohort (NHISHEALS), including 247,696 participants free from any CVD history recruited between 2002 and 2003, reported an increased number of dental caries lesions, the presence of periodontitis and a greater loss of teeth were all associated with an increased risk of future major cardiovascular events (MACEs), including cardiovascular death, acute myocardial infarction, heart failure and stroke [91]. One additional toothbrushing episode per day was associated with a reduced incidence of ACVD events (HR = 0.91, 95% CI [0.89, 0.93]), and regular professional cleaning reduced the risk even further (HR = 0.86, 95% CI [0.82; 0.90]).
In summary, progression of ACVD may be influenced by successful periodontal treatment independent of traditional CVD risk factor management.
There is only one pilot multi-centre study on secondary prevention of ACVD events (PAVE: [21, 88]), which reported no statistically significant difference in the rate of CVD events between patients who underwent treatment of periodontitis versus community care (risk ratio –RR = 0.72, 95% CI [0.23; 2.22]). Several methodological limitations highlighted in the trial limit the applicability/usefulness of such evidence to inform the research and healthcare communities.
Thus, there is insufficient evidence to support or refute the potential benefit of the treatment of periodontitis in preventing or delaying ACVD events [61].
Table 1 summarizes the evidence on the effect of periodontal therapy on surrogate markers of CVD. There is moderate evidence for reduction of low-grade inflammation as assessed by serum levels of CRP, IL-6 and improvements in surrogate measures of endothelial function (flow-mediated dilatation of the brachial artery).
Table 1
Summary of the evidence on the effect of periodontal therapy on surrogate markers of cardiovascular diseases.
| Topic | Outcome | Number of RCTs and SR since last consensus | References | Effect | Overall Level of Evidence |
|---|---|---|---|---|---|
| Effect of Periodontal Therapy on Lipids | Lipids (multiple) | 6 RCTs | [12, 22, 26, 38, 44, 51] | No | Moderate |
| Effect of Periodontal Therapy on Blood Pressure | Systolic, diastolic | 3 RCTs | [22, 44, 142] | Yes | Limited |
| Effect of Periodontal Therapy on Endothelial Function | Endothelial Function (multiple measures) | 2 RCTs | [22, 105] | Yes | Moderate |
| 1 SR | [122] | ||||
| Effect of Periodontal Therapy on interleukin (IL)-6 | IL-6 | 3 RCTs | [38, 51, 142] | Yes | Moderate |
| Effect of Periodontal Therapy on C-Reactive Protein (CRP) | CRP | 5 SR | [27, 37, 49, 90, 125] | Yes | Moderate |
| 7 RCTs following 2014 | [12, 22, 26, 44, 51, 53, 142] | ||||
| Effect of Periodontal Therapy on Pulse Wave Velocity (PWV) | PWV | 1 RCT | [51] | No | Limited |
| Effect of Periodontal Therapy on carotid Intima-Media Thickness (c-IMT) | Common c-IMT | 1 RCT | [51] | Yes | Limited |
RCT, randomised clinical trial; SR, systematic review.
Moderate evidence suggests periodontal treatment does not have an effect on lipid fractions, whilst there is limited evidence suggesting periodontal treatment reduces arterial blood pressure and stiffness, subclinical ACVD (as assessed by mean carotid Intima-Media-Thickness), and there is insufficient evidence of an effect on ACVD biomarkers of coagulation, endothelial cell activation and oxidative stress.
Statins are medications prescribed to decrease LDL cholesterol. Numerous trials have demonstrated their benefit for the prevention of cardiovascular diseases [141].
Interestingly, statins possess various additional properties relevant to the pathogenesis and treatment of periodontitis [34]. In particular, it has been reported that statins are anti-inflammatory [54, 94, 97, 102, 106], can promote bone formation [41, 67, 81, 134], can inhibit matrix metalloproteinases (MMPs) [54, 71, 96] and possess anti-microbial properties [126].
A systematic review with meta-analysis of pre-clinical in vivo trials reported a positive effect of local or systemic statin administration for the prevention of alveolar bone loss in experimental periodontitis models in rodents [9].
Several observational clinical studies have evaluated the effect of systemic statin intake on periodontal conditions [65, 76, 107, 109, 110, 123]. Statin use was not found to be associated with decreased tooth loss in adults with chronic periodontitis when analysing administrative health plan data [109]. However, a five-year population-based follow-up study comparing participants treated with statins with those who did not medicate with statins concluded long-term treatment with statins was associated with reduced tooth loss [76]. Furthermore, patients on statin medication were reported to exhibit significantly fewer signs of periodontal inflammatory lesions than patients without a statin regimen [65]. A cross-sectional study compared the periodontal status of patients with hyperlipidaemia (with or without statin intake) to normolipidaemic individuals and found higher gingival bleeding and probing depths in the hyperlipidaemic patients who were not statin users [107]. In an RCT, periodontal patients with risk factors or with established atherosclerosis were assigned to either a high or low dose statin intake [123]. After three months, a significant reduction of periodontal inflammation was seen in the high-dose compared to the low-dose group. Thus, within the limits of the above reported studies, there is some limited evidence suggesting statins may have a positive impact on periodontal health.
Very few clinical studies have been designed to evaluate the effect of adjunctive systemic statin intake in conjunction with periodontal therapy [35, 36, 108]. In a randomized placebo-controlled pilot study in 38 patients with chronic periodontitis, adjunctive statin intake led to beneficial effects on radiological bone loss and tooth mobility after 3 months [35]. Another 3 month-study compared the treatment response to nonsurgical periodontal therapy in 107 chronic periodontitis patients (35 normolipidemic as control, 36 hyperlipidaemic on nonpharmacological therapy and 36 hyperlipidemic on statins) and found a greater improvement in gingival index in the nomolipidemic control and in the statin groups [108]. Based on this limited evidence, two recent systematic reviews with meta-analysis on the effects of (local and systemic) statins on periodontal treatment concluded systemic statin intake does not enhance the outcomes of periodontal therapy [8, 82].
Non-surgical treatment of periodontitis involving supra- and sub-gingival instrumentation of the affected dentition (under local anaesthesia) is often delivered in several short sessions. Alternatively, full-mouth non-surgical periodontal treatment can be performed within 24 hours.
Delivering periodontal treatment in a full-mouth fashion (i.e., within 24 hours) triggers a one-week acute systemic inflammatory response associated with a transient impairment of endothelial function [89]. This distant effect is not observed when periodontal treatment is delivered across several separate sessions [42]. This is achieved by limiting the number of teeth involved and the time devoted to completing the dental instrumentation. These findings raise the question of whether performing longer sessions of periodontal treatment could contribute to an individual’s inflammatory burden/risk and increase their short-term risk of suffering from a vascular event. There is consistent and strong observational evidence that common acute infections/inflammatory responses are associated at a population level with an increased risk of vascular events within the first four weeks of the infectious/inflammatory event [120].
There is no evidence for specific effects of periodontal treatment procedures on increasing ischemic cardiovascular risk. Two observational studies reported no effect of invasive dental treatment in elevating ischemic cardiovascular risk [19, 86], and one study suggested a minimal increased risk within four weeks following treatment [79].
Chen et al. [19] performed a case-crossover and self-controlled case series using the Taiwanese National Health Insurance Research Database, including over 110,000 myocardial Infarction cases and 290,000 Ischemic Stroke patients, between 1999 and 2014. They reported a non-significant increase in the incidence of myocardial infarction within the first 24 weeks following invasive dental treatment (including periodontal procedures) except for a modest risk of myocardial infarction during the first week for patients without other comorbidities (OR = 1.31, 95% CI [1.08; 1.58], after 3 days).
A registry-based case-control study between 2011 and 2013 including 51,880 cases who underwent an invasive dental procedure compared to 246,978 controls reported no association with increased incidence of myocardial infarction (OR 0.98, 95% CI [0.91; 1.06]) [86].
Minassian et al. [79] performed a self-controlled case series including nearly 10 million participants included in an insurance database from 2002 and 2006 in the USA. The analysis showed that invasive dental treatment (largely comprising of tooth extractions and only 4% being non-surgical and surgical periodontal procedures) is associated with an increased risk of incident acute cardiovascular events (IR = 1.5, 95% CI [1.09; 2.06]) within the first four weeks of treatment recorded.
In summary, the Group concluded delivering periodontal treatment is safe with regard to cardiovascular risk.
There is limited evidence on the effects of invasive dental treatment on the incidence of Ischemic Events in patients with established CVD or after an event.
A small RCT on the effects of the treatment of periodontitis on CVD biomarkers in patients with established CVD [80] showed no cardiovascular adverse events within three months of completion of scaling and root planing (periodontal therapy).
In the PAVE feasibility randomized secondary prevention trial, provision of periodontal scaling and root planing treatment in patients with established CVD did not increase the incidence of cardiovascular events compared to the control group (community treatment) within six months [6].
In summary, the Group concluded delivering periodontal treatment is safe with regards to cardiovascular risk in patients with established CVD.
Periodontal treatment consists of numerous procedures with different levels of bleeding risk. However, this risk of bleeding is low in the vast majority of procedures and can be easily controlled with local haemostatic measures.
Perioperative bleeding risk varies according to the extent and invasiveness of the periodontal procedure performed. The majority of periodontal procedures may be grouped within the ESC/AHA/EHRA [121, 122]. Low Bleeding Risk (frequency less than 1% of post-operative bleeding) group: supragingival polishing, non-surgical periodontal treatment, conventional surgical periodontal treatment (conservative, resective or regenerative), tooth extractions and dental implant placement. Moderate bleeding risk (frequency between 2–5%) may be observed in major autogenous bone augmentation procedures, such as block bone harvesting, sinus floor elevation and procedures where healing is by secondary intention, such as free gingival grafting. Appendix 1 summarizes the main recommendations for patients with antithrombotic therapy when perfoming periodontal therapy.
Individuals undergoing single acetylsalicylic acid (ASA) therapy (aspirin) in different therapeutic dosages, as well as therapy with clopidogrel, ticlopidine or ticagrelor show no statistically significant differences in frequency of bleeding events when compared to controls (i.e., subjects not undergoing anti-platelet therapy) [30, 62].
Dual antiplatelet therapy, most commonly ASA in combination with clopidogrel, may pose a certain risk for postoperative bleeding complications; however, it appears these haemorrhagic events may be managed safely with local haemostatic measures [84, 85].
Thus, current evidence does not support discontinuation of antiplatelet therapy before dental procedures, irrespective of the type of therapy employed (single or dual antiplatelet therapy) or the type of procedure performed (single, multiple tooth extractions, non-surgical and surgical periodontal therapy and dental implant procedures).
In patients taking oral anticoagulant therapy (vitamin-K antagonists, VKA) and undergoing dental extraction, minor dental procedures and dental implant placement do not seem to increase the risk of bleeding compared to patients who discontinue oral anticoagulant therapy [118, 139]. There may be a higher post-operative bleeding risk in patients continuing VKA and undergoing either minor dental surgery or other higher-risk procedures when compared to non-VKA patients [10, 118], but local haemostatic agents appear to be effective in controlling post-operative bleeding [72].
Limited trials and evidence are available on the management of patients on novel oral anticoagulant (NOAC) therapy undergoing dental treatment; hence, the Group concluded further studies regarding dental procedures in these patients are strongly encouraged.
It appears there is no need for interruption of NOAC therapy in most dental treatments due to a low incidence of bleeding complications, which can be successfully managed with local haemostatic measures when comparing groups continuing NOAC and groups discontinuing NOAC therapy [58, 59, 92, 137], and with reported timing of discontinuation and reinstitution varying greatly. When comparing NOAC patients with healthy individuals, there seems to be a higher incidence of delayed bleeding (2 days and later) in those patients who do not discontinue NOAC therapy [78].
However, attention should be paid to:
Current AHA/ACC/SCAI/ACS/ADA/ESC/ACCP guidelines on perioperative management of antithrombotic therapy do not suggest discontinuation of anti-platelet therapy for Low Bleeding Risk procedures [32, 43, 57].
Various approaches for perioperative management of anticoagulant therapy have been suggested. The Group reviewed the guidelines on perioperative management of vitamin K antagonists (VKA) and suggests discontinuation of medication treatment if the INR is 4 or below for Low or Medium Bleeding Risk procedures [95]. However, if the internationalised normalised ratio (INR) is 3.5 or above, the expert Group recommends dental clinicians seek advice and consult with the responsible medical professional. Management of high thromboembolic risk cases should be collaborative in consultation with the medical professional responsible for the VKA therapy [57, 130].
After reviewing novel anticoagulant (non VKA) and direct anticoagulant (NOAC/DOAC) therapies guidelines, the Group concluded that for Low Bleeding Risk periodontal procedures no discontinuation of anticoagulants is recommended [121, 122]. These procedures could be performed 18–24 hrs after the last intake (depending on a renal function assessment for the medication in question) and then restarted 6 hrs following treatment. The expert Group, however, strongly recommends the dental clinician consult with the responsible medical professional. When a Medium Bleeding Risk periodontal procedure is planned, discontinuation of therapy should be agreed with the medical professional responsible for and/or prescribing the anticoagulant therapy.
Lastly, in cases of combined anti-platelet and anticoagulant therapies, which pertain to patients with the highest thrombotic and ischemic risk (i.e., chronic atrial fibrillation or after an acute myocardial infarction or recent coronary stenting), when periodontal procedures (either of Low or Medium Bleeding Risk) are required, any alterations in medication should be discussed and agreed upon with the responsible medical professional [121, 122]. In elective periodontal procedures, the operation should be delayed until after treatment stabilization and appropriate consultation with the medical specialist.
In cases of triple therapy (dual anti-platelet and one anticoagulant) or one anticoagulant plus one anti-platelet, such patients need individualised management by the responsible medical professional according to their thrombotic and haemorrhagic risk [130].
It is important to highlight that local haemostatic agents (such as oxidised cellulose, absorbable gelatin sponges, sutures, tranexamic acid mouthwashes, compressive gauze soaked in tranexamic acid) should be used and dental clinicians should consider the confounding effect of local anaesthetic with vasoconstrictors.
Because of the potential negative impact of periodontitis on CVD complications, the following recommendations are made:
This may include
Dentists should be able to identify the early signs of gum disease, but patients should also suspect gum disease if noticing
Patients should inform their dentist about the outcome of their visits to the physician and provide an update on their CVD history and any changes in medications. Patients should inform the dentist if they are on anticoagulant therapy.
Patients should understand it is important to keep their mouth and whole body as healthy as possible with regular dental and medical visits.
If your physician has told you that you have cardiovascular disease (CVD), you should make an appointment with a dental surgeon to have your mouth and gums checked.
This is because people with CVD may have a higher chance of getting further complications when they have gum disease. The earlier you seek help, the better the outcome will be.
You may have gum disease if you have ever noticed
If you have noticed any of these problems, it is important to see a dentist as soon as possible.
Gum disease may also be present and get worse with no apparent that you have it, especially if you smoke, so even if you do not think you have gum disease now, you should still have annual check-ups of your mouth as part of managing your CVD. Your dentist will be able to pick up early signs of gum disease.
You need to clean your teeth and gums twice daily at home for a minimum of two minutes. Also, cleaning between your teeth daily is important, and your oral health professional will show you how to do this. You should visit a dental surgeon as soon as possible for a diagnosis and advice on what you need to do. It is important to keep your mouth as healthy as possible with regular oral and dental care, according to the recommendations of your oral health professional.
The additional file for this article can be found as follows:
Supplementary Appendix 1Antithrombotic therapy: when, how and why. Comprehensive approach for oral health professionals. DOI: https://doi.org/10.5334/gh.400.s1
This workshop was funded through an unrestricted grant from DENTAID SA to the European Federation of Periodontology to organize the EFP/EHF Workshop. All individual experts participating in the workshop have declared no conflict of interest with the results of the consensus workshop or the publication.
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