https://doi.org/10.52418/moldovan-med-j .64-4.21.05 0 /^Access
UDC: 616.314-089.843
The general condition of patients requiring the alveolar bone crest reconstruction
Alexandru Ghetiu
Arsenie Gutan Department of Oral and Maxillofacial Surgery and Oral Implantology Nicolae Testemitanu State University of Medicine and Pharmacy, Chisinau, the Republic of Moldova
Corresponding author - Alexandru Ghetiu, e-mail: [email protected] Manuscript received July 27, 2021; revised manuscript October 05, 2021; published online October 12, 2021
Abstract
Objectives: To present the survey questionnaire used for the medical assessment of patients requiring alveolar ridge reconstruction as well as the study of concomitant pathologies and their influence on the healing process.
Material and methods: The study involved 173 patients aged between 18 and 69 years. All patients have been assessed according to the survey questionnaire developed to determine the patient's general condition, life anamnesis, and medical history.
Results: Out of the total of 173 patients, 72 (41.6%) had no concomitant pathologies, 8 patients (4.6%) had concomitant pathologies that did not interfere with the operation, 40 (23.1%) had pathologies that might affect the outcome of alveolar ridge reconstruction but still were admitted to surgery, and 53 patients (30.6%) had pathologies that could affect the outcome of the reconstruction procedure and were not admitted to bone grafting. Conclusions: Assessment of patients with alveolar ridge defects during preparation and planning of preimplantation bone reconstruction identified a number of concomitant pathologies, more or less noticed by the patient, which may remain unclear due to superficial study of the patient's condition that is able to influence the surgical treatment outcome. These issues can be both intraoperative and postoperative and lead to failure of surgical treatment and further reoperation.
Key words: alveolar ridge reconstruction, systemic conditions.
Cite this article
Ghetiu A. The general condition of patients requiring the alveolar bone crest reconstruction. Mold Med J. 2021;64(4):29-34. https://doi.org/10.52418/ moldovan-med-j.64-4.21.05.
Introduction
In our days, implant treatment of toothless is the most elected method. Chele et al. propose the immediate post extraction implant placement [1], however, in cases of alveolar ridge deficiency additional bone growth is needed. In 2016, Knofler W. et al. showed that bone growth procedures associated with dental implants are required in 58.2% of cases [2]. Postoperative healing after bone grafting is directly influenced by the general condition of the body. Thus, in addition to the thorough study of the affected area, the assessment of the patient's general condition and concomitant diseases are equally important for the rehabilitation of edentulous patients with severe mandibular atrophy.
A multitude of alveolar grafting methods are proposed in preimplantation. In literature, there are studies on guided bone regeneration, which is the most widely used method of alveolar grafting showing high efficacy [3].
Guided bone regeneration (GBR) is an extremely delicate procedure that relies on body's ability of self-healing. Therefore, patients with poor healing potential cannot undergo GBR procedures. Systemic conditions that may impede the patient to undergo surgery include a number of general medical conditions such as: uncontrolled diabetes mellitus, tumors, recent radiation of the head and neck rei (S9
gion, acquired immunodeficiency syndrome (AIDS) or other conditions that cause immunosuppression, decompen-sated systemic conditions, cardio-vascular diseases, etc. [4]. Cardiovascular diseases are systemic conditions that highly affect tissue regeneration as they disrupt the nutrition and oxygenation of tissues through vascular damage. These types of diseases are extensively evaluated while preparing patients for preimplantation. Cardiovascular diseases are among the most common systemic conditions. Patients with cardiovascular diseases may develop medical conditions such as: congestive heart failure, angina pectoris, myocardial infarction, cardiac arrhythmia, heart valve prosthesis, pacemaker, hypertension, anticoagulant addiction, and post-extraction dental hemorrhage (PDH) [5].
Patients may also suffer from general diseases and conditions such as: infectious endocarditis, diabetes mellitus, osteoporosis, hormonal medication, radiotherapy, gastro-esophageal reflux disease (GERD), systemic lupus erythematosus, HIV infection, smoking status, and stress. All these diseases may have a different impact on alveolar ridge reconstruction. Often, because of the focus on local diseases doctors neglect the assessment of body's general condition. A general pathology may go unnoticed if the patient does not communicate about it. All causes mentioned above, as well as superficial examination of the patient can generate poor
results and failure of clinical outcomes. Thus, it is imperative to detect concomitant pathologies and study their impact on alveolar ridge reconstruction.
This study is to assess the general medical condition of patients requiring alveolar ridge reconstruction. To study the concomitant pathologies and their influence on the healing process after bone grafting.
Material and methods
The study took place between 2016 and 2020. There were assessed 173 patients aged between 18 and 69 years and the mean age constituted 46.7±0.3 years (84 men and 89 women).
All patients have been assessed according to a survey questionnaire that was developed to determine the patient's general condition, life anamnesis, and medical history. The first part contains information about the patient's personal data. The second part is filled in by the doctor and contains information about oral hygiene, smoking status, smile line and aesthetic expectations of the patient. The third part of the survey questionnaire contains a set of questions to which the patient answers by ticking the options, if necessary; additionally it states information about the disease.
List of patient's questions:
0 Do you suffer/ have you suffered from any acute or chronic diseases?
0 Do you suffer/ have you suffered from: disorders of the immune system; allergies or drug/nonmedicinal intolerances; hypertension; vascular diseases; heart disease; respiratory diseases; gastrointestinal diseases; hepatobiliary diseases; kidney and/or urinary diseases; neurological diseases; mental illness; eye diseases; hematological diseases; endocrine diseases; diseases of the skeleton; diseases of the skin and mucous membranes; tumors; obstructive sleep apnea?
0 Are you following any treatment (medicinal, homeopathic, phytotherapy)?
0 Have you been on any treatment with: antibiotic in the last month, anticoagulants, or bisphosphonates?
0 Are you having difficulty breathing?
0 Do you have / have you had any vicious habits?
0 Have you undergone any surgery in your lifetime?
0 Have you had dental treatment before?
0 Have accidents/incidents or complications occurred in previous dental treatments?
0 Have you ever donated blood?
0 Are you pregnant?
In the study all patients have had severe alveolar ridge atrophy requiring reconstruction and further implant-prosthetic rehabilitation. By using the survey questionnaire, the presence or absence of general pathologies was evaluated and some of the patients were accepted for bone grafting. Other patients were not engaged in bone reconstruction surgery because of concomitant pathologies occurrence associated with absolute contraindications. The selected patients were assessed according to evaluating postoperative healing parameters at 7 days, 21 days, and 6 months (implantation stage). The influence of general pathology on healing pro-
cess was also taken into account. The healing parameters were: wound dehiscence, mucosal erosion, and graft exposure. These parameters have been analyzed after clinical and paraclinical aspects by using pictures. The data obtained was entered into a Microsoft Excel table and analyzed statistically using IBM SPSS Statistics 22.
Results and discussion
Out of the total 173 patients, 72 (41.6%) had no concomitant pathologies, 8 patients (4.6%) had concomitant pathologies that did not interfere with the operation, 40 (23.1%) had pathologies that could affect the outcome of alveolar ridge reconstruction but still were admitted to intervention, and 53 patients (30.6%) had pathologies that could affect the outcome of the reconstruction and were not admitted to bone grafting. 53 (100%) patients who were not admitted to bone reconstruction had the following general pathologies and vices (tab.1.): osteoporosis treated with intravenous bisphosphonates (3-5.7%), cardiopathies or angiopathies treated with oral anticoagulants (7-13.2%), compensated or decompensated diabetes mellitus (14-26.4%), long-term treatment of pemphigus with corticosteroids that decreases osteogenesis and creates immunosuppression (1-1.9%), long-term treatment of osteoarthritis with corticosteroids that decreases osteogenesis and creates immunosuppression (2-3.8%), radiotherapy performed no less than 12 months after the last cure (5-9.3%), chemotherapy performed no less than 6 months after the last cure (3-5.7%), rheumatoid arthritis treated with cytostatic (7-13.2%), hemophilia (23.8%), non-compliant heavy smokers (more than 10 cigarettes/day) (8-15.1%), after use of intravenous phosphate drugs (current consumption in suspension) (1-1.9%).
Table 1. Patients with general pathologies and unaccepted vices for bone reconstruction
General pathologies and vices Patient No Percentage
Osteoporosis treated with intravenous 3
bisphosphonates
Cardiopathies or angiopathies treated with 7 13.2%
oral anticoagulants
Compensated or decompensated diabetes mellitus 14 26.4%
Long-term treatment of pemphigus with 1 1.9%
corticosteroids
Long-term treatment of osteoarthritis with 2
corticosteroids
Radiotherapy /no less than 12 months after 5 9.3%
the last cure
Chemotherapy /no less than 6 months after 3
the last cure
Rheumatoid arthritis treated with cytostatic 7 13.2%
Hemophilia 2 3.8%
Non-compliant heavy smokers 8 15.1%
After use of intravenous phosphate drugs 1 1.9%
Total 53 patients 100%
40 patients (100%) had pathologies and vices that could affect the outcome of alveolar ridge reconstruction but still were admitted to intervention (tab. 2). These pathologies are: hyperparathyroidism (osteoporosis) (1-2.5%), hypothyroidism (osteoporosis) (4-10%), Crohn's disease (osteoporosis caused by malabsorption of D2 and calcium in the intestine) (2-5%), gastroesophageal reflux disease (5-12.5%), compensated diabetes (18-45%), and light smokers (up to 10 cig/ day) (10-25%).
Table 2. Patients with general pathologies and vices admitted to bone reconstruction
General pathologies and vices Patient No Percentage Local complications
Wound dehiscence Erosion of the mucosa with graft exposure
Hyperparathyroidism 1 2.5% 0 - 0% 1 - 2.5%
Hypothyroidism 4 10% 1 - 2.5% 0 - 0%
Crohn's disease 2 5% 0 - 0% 0 - 0%
Gastrointestinal reflux disease 5 12.5% 2 - 5% 1 - 2.5%
Compensated diabetes 18 45% 6 - 15% 1 - 2.5%
Light smokers 10 25% 3 - 7.5% 1 - 2.5%
Total 40 100% 12 - 30% 4 - 10%
Other 8 (100%) patients had the following concomitant pathologies that did not interfere with alveolar ridge reconstruction (tab. 3): drug allergy (3-37.5%), hepatitis B infection (2-25%), chronic bronchitis (2-25%), and renal lithiasis (1-12.5%).
table 3. Patients with concomitant pathologies that do not interfere with bone reconstruction surgery
Local complications
General Patient Percen- Wound Erosion of
pathologies No tage dehis- the mucosa
cence with graft
exposure
Drug allergy 3 - 37.5% 37.5% 0 0
Hepatitis B 2 - 25% 25% 0 0
Chronic bronchitis 2 - 25% 25% 0 0
Renal lithiasis 1 - 12.5% 12.5% 0 0
Total 8 patients 100% 0% 0%
The majority of patients (72) admitted to surgery did not have concomitant pathologies or vices (tab. 4).
table 4. Patients without concomitant pathologies and complications admitted to bone reconstruction
General pathologies Patient No Percentage Local complications
Wound dehiscence Erosion of the mucosa with graft exposure
No pathologies 72 100% 1 - 1.4% 5 - 7%
The presence of complications was studied in patients who underwent alveolar ridge reconstruction. Concomitant pathology which is influencing the outcome of alveolar ridge reconstruction can lead to high rate of exacerbations. Thus, out of 72 patients (100%), 1 patient (1.4%) had wound dehiscence and 5 patients (7%) had mucosal erosion with graft exposure. All these patients, who experienced complications were completely healthy without concomitant pathologies. Patients with general pathologies that did not influence bone reconstruction (8 patients) had no postoperative complications. 40 (100%) patients who had pathologies that could affect the outcome of alveolar ridge reconstruction showed wound dehiscence in 12 cases (30%) and erosion of the mucosa with graft exposure in 4 cases (10%).
The positive outcome of bone reconstruction surgery is closely related to bone structure characteristics. Bone tissue is a dynamic highly organized structure that can be remodeled according to mechanical stress and hormonal activity. The resorbed bone is replaced by the forming cells and the bone neoformation, which lasts approximately 3 months [6]. Another component of the positive outcome of bone reconstruction procedures is related to body condition when various intra- and postoperative complications may occur but they are not directly related to bone healing. These conditions and their management are described below [7].
Some cardiovascular pathologies are treated with anticoagulant medication. These can lead to immediate and delayed complications with harmful consequences or alveolar ridge reconstruction failure. Zanoaga O. et al. showed that dental extractions can be carried out without cancelling the administration of antithrombotic drugs [8]. Two classes of new oral anticoagulants are currently available for this purpose: thrombin inhibitors (dabigatran) and factor Xa inhibitors (rivaroxaban, apixaban, edoxaban). Unlike vitamin K inhibitors (acenocoumarol, warfarin), which block the formation of several active vitamin K-dependent factors (factors II, VII, IX and X), new oral anticoagulants block the activity of a single factor in the blood clotting cascade [8]. These new oral anticoagulants are: Dabigatran etexilate (brand name Pradaxa), Rivaroxaban (brand name Xarelto), Apixaban (brand name Eliquis), and Edoxaban (brand name Lixiana).
Cardiac pathology and increased risk of endocarditis should be considered in the oral surgical patient. Patients with valvular prostheses, history of infectious endocarditis, as well as those with cyanogenic congenital heart disease may develop infectious endocarditis, which remains a severe form of valvular dysfunction associated with poor prognosis and high mortality. In 2018, Zanoaga O. showed that dentoalveolar surgery requires prophylaxis of the infective endocarditis [9].
Glucose metabolism disease influences the tissue healing. Uncontrolled diabetes was associated with greater variability and increased rate of infectious complications in alveolar ridge reconstructions; insulin-mediated metabolic control can reverse these adverse effects [10].
The high rate of complications, such as resorption, non-
integration and delayed healing of bone graft, especially in the upper jaw, can occur in patients with osteoporosis. Generally, osteoporosis is not a contraindication for bone augmentation and placement of dental implants. Although, an increase of risk factors and complications can be expected in patients with osteoporosis [11]. A number of therapeutic approaches have been proposed to accelerate bone healing and prevent complications in bone grafting. These treatments include bisphosphonates, hormone replacement therapy (HRT), calcitonin, diet high in vitamins and calcium supplements [12]. The cornerstone of osteoporosis prevention and treatment is the provision of adequate intake of calcium, vitamin D and weight-bearing exercises. It is known that mechanical demand produces an increase of the cellular metabolism and collagen synthesis. There are studies showing that physical exercises are beneficial for preventing bone loss in postmenopausal women. Smoking is a risk factor for osteoporosis and is also associated with high rate of implant failure [13]. A combination of osteoporosis and tobacco intake leads to a high complication rate, thus, quitting smoking is imperative for a positive outcome of bone reconstruction in patients with osteoporosis. Other risk factors for osteoporosis are the use of corticosteroids and increased consumption of alcohol and caffeine. Patients with osteoporosis should be encouraged to reduce alcohol and caffeine intake before dental implant surgery or bone grafting.
Currently, it is unknown if the use of systemic bisphos-phonates for the treatment of osteoporosis influences directly or indirectly the capacity of guided bone regeneration (GBR) techniques [14]. Bisphosphonates are the synthetic analogues of inorganic pyrophosphate. The most common oral drugs used in the treatment of osteoporosis are: alen-dronate, risedronate and ibandronate. They have been shown to reduce osteoclast activity and therefore bone resorption [15]. Recently, bisphosphonates have been associated with jaw osteonecrosis. Most cases of necrosis are, however, associated with intravenous administration of high doses of pamidronate and zoledronate, which are commonly used for bone metastases treatment in multiple myeloma and breast cancer. Treatment with oral bisphosphonates may be considered as risk factor for osteonecrosis [16].
In 2008, Radzichevici M. showed that the excess of phosphorus accumulates in tissues. Phosphorus binds with calcium and is retained in the bone in large quantities sclerosing and destroying bone vascular and nerve endings. Thus, the oral cavity appears to be "the gate of infection" that communicates with the jaw bones through the periodontium [17]. In this way the mechanism of overinfection of jaw bones can be explained. The high risk of failure or occurrence of postreconstruction osteonecrosis in patients who administer or have administered narcotic phosphorus substances emphasizes the importance of a full preoperative assessment.
Long-term administration of corticosteroids within systemic pathologies has negative impact on the body, i.e. on marginal periodontium and alveolar ridge reconstruction. Corticosteroid therapy has an adverse effect on the bone system and can induce osteoporosis [18]. Regarding the alveo-
lar ridge reconstruction in long-term corticosteroid therapy it is reasonable to assess the risk induced by corticosteroid-induced osteoporosis [19].
After radiotherapy osteoblasts and osteoclasts decrease quantitatively and the terminal differentiation of osteoblasts is accelerated. Data published showed that mesenchymal stem cells in the bone marrow are quantitatively reduced [20]. Vascular sclerosis and fibrosis are characteristic features of radiation injury. Spontaneous bone healing is highly compromised and reduced in irradiated areas and the physiology of bone regeneration is modified as well [21]. One of the most important life-threatening adverse effect is osteo-radionecrosis. Ionizing radiation limits the vascularization, increases the incidence of fibrous union, and leads to high morbidity rate. Bone grafts cannot be used when vascular system is in poor condition [22]. Therefore, alveolar ridge reconstruction should be considered from 12 months after the last course of radiotherapy.
Gastric pathologies have a great impact on the oral cavity state, as well they affect the rehabilitation after oral surgery. Gastroesophageal reflux disease GERD constitutes the risk factor for chronic marginal periodontitis; therefore, it can influence the outcome of alveolar ridge reconstruction. The most reasonable explanation is the reduction of salivary gland functioning. Mixed saliva covers all vital internal anatomical surfaces with secretions rich in mucin that provide a diffuse protective barrier against mechanical, thermal, chemical and microbial damage. Saliva also acts as an endogenous antacid agent that acts against symptomatic gastroesophageal reflux disease. Therefore, the decrease of salivary secretion leads to insufficient acid neutralization [23]. Hyposalivation in patients with GERD has been demonstrated in several studies. It was found an association between reduced salivary flow and periodontal disease among the elderly [24]. Therefore, we can conclude that hyposalivation in GERD may have an influence on the development of chronic periodontitis by allowing the proliferation of intraoral bacteria, thus increasing the risk of infection of grafts and materials used in alveolar ridge reconstructions. Therefore, dental surgeons should manage GERD in patients requiring alveolar ridge reconstruction.
In 2016, Adachi et al. showed that the degree of endo-scopic atrophy of the gastric mucosa in patients with marginal periodontitis was significantly higher compared to those without periodontitis [25]. Long-term H. pylori infection causes not only atrophy of the gastric mucosa, but also marginal periodontitis. Therefore, it is reasonable to treat H. pylori before alveolar ridge reconstruction. This measure will help to control periodontopathic bacteria and prevent complications after reconstruction.
HIV-positive patients may be candidates for alveolar bone reconstruction. These immunocompromised patients may be incapable for sustained, controlled and effective immune response to exogenous trauma that constitutes a high risk for developing further postoperative complications. Thus, HIV-positive patients have a high postoperative infection rate after rehabilitation of maxillofacial trauma (11.8%
vs 4.4% HIV-negative) [26]. The hypothesis of a higher risk for HIV-infected patients after oral surgery has been presented [27]. No relationships between complications and vi-rologic or immunological laboratory parameters were found.
A special category of patients requiring alveolar ridge reconstruction are smokers. Although, smokers may not have general pathologies that could influence the outcome of alveolar ridge reconstruction there is a risk associated with smoking consequences on tissues and structures of the oral cavity. Smoking has been associated with increased accumulation of bacterial plaque; high incidence of gingivitis and periodontitis; high rate of tooth loss and increased resorption of the alveolar bone; and poor mucogingival healing after surgery due to frequent occurrence of refractory periodontitis. Several studies have shown that smoking was a risk factor for marginal bone loss or implant failure [28]. Some authors suggest that better results can be achieved in smokers if an aggressive antimicrobial regimen is followed
[29], however, the results obtained after keeping this regimen are not as favorable as those obtained in non-smokers.
Particular attention should be paid to patients aged 60 years old or over (geriatrics) while performing alveolar ridge reconstruction. Being a geriatric patient is not a contraindication for implant treatment and alveolar ridge reconstruction. Healthy elderly patients without systemic conditions can have dental implants and there is no evidence that geriatric changes of bone metabolism affect directly the osseoin-tegration. According to Hyo-Jung Lee et al. implant therapy in geriatric patients should not be considered a risk factor
[30]. It is imperative to assess the general state of the geriatric patient that is a candidate for oral reconstructive surgery and take a therapeutic decision according to obtained results.
The study allowed us to identify some steps (fig. 1) for the guidance of specialists that have to elect patients with general diseases for alveolar ridge reconstruction [29].
Fig. 1. Decision tree for determining whether the patient is a candidate for GBR, based on their systemic conditions [29]
The fact that 10% of all patients presented concomitant pathologies that can influence the alveolar ridge reconstruction highlights the importance of anamnesis and a thorough preoperative preparation in order to maximize the positive outcome of alveolar ridge reconstruction.
Conclusions
The study has shown the existence of: high rate of postoperative complications after alveolar ridge reconstruction in patients with concomitant pathologies, which are able to influence the healing process; low complication rate or its absence when concomitant pathologies are lacking; pathologies that cannot influence the healing process. Assessment of patients with alveolar ridge defects during preparation and planning of preimplantation bone reconstruction identified a number of concomitant pathologies, more or less noticed by the patient, which may remain unclear due to superficial study of the patient's condition that is able to influence the surgical treatment outcome. These issues can be both intraoperative and postoperative and lead to failure of surgical treatment and further reoperation.
References
1. Chele N. Implantarea dentara imediata: riscuri si beneficii [Immediate dental implantation: risks and benefits]. Chisinau; 2017. 272 p. Romanian.
2. Knofler W, Barth T, Graul R, Krampe D. Retrospective analysis of 10000 implants from insertion up to 20 years-analysis of implantations using augmentative procedures. Int J Implant Dent. 2016 Dec;2(1):25. doi: 10.1186/s40729-016-0061-3.
3. Jensen SS, Terheyden H. Bone augmentation procedures in localized defects in the alveolar ridge: clinical results with different bone grafts and bone-substitute materials. Int J Oral Maxillofac Implants. 2009;24:218-236.
4. Cooper LF, Masuda T, Yliheikkila PK, Felton DA. Generalizations regarding the process and phenomenon of osseointegration. Part II. In vitro studies. Int J Oral Maxillofac Implants. 1998 Mar-Apr;13(2):163-174.
5. Lusk KA, Snoga JL, Benitez RM, Sarbacker GB. Management of direct-acting oral anticoagulants surrounding dental procedures with low-to-moderate risk of bleeding. J Pharm Pract. 2018 Apr;31(2):202-207. doi: 10.1177/0897190017707126.
6. Sirbu D, Topalo V, Chele N, et al. Regenerarea osoasa in reabilitarea implanto-protetica a pacientilor cu defecte ale oaselor maxilare [Bone regeneration in the rehabilitation process of patients with defects of the maxillary bones]. Med Stomatol. 2016;1(38):33-42. Romanian.
7. Ghetiu A, Sirbu D, Chele N, Bran S, Jurjiu V, Nosaci A. Crearea ofertei osoase a maxilarului superior cu atrofie avansata in reabilitarea implanto-protetica prin grefa osoasa autogena din creasta iliaca [Reconstruction of the upper jaw bone volume with advanced atrophy in the implant-prosthetic rehabilitation by autogenous bone graft from the iliac crest]. Med Stomatol. 2019;4(53):9-18. Romanian.
8. Zanoaga O. Anticoagulantele orale noi in practica medicului stoma-tolog [New oral anticoagulants in dental practice]. Med Stomatol. 2019;4(53):46-52. Romanian.
9. Zanoaga O, Frasineanu D, Zgircea A, Mostovei A, Hachi G. Antibio-ticoprofilaxia in stomatologie la pacientii cu risc sporit de endocardita infectioasa [Antibiotic prophylaxis in dentistry in patients with an increased risk of infectious endocarditis development]. Med Stomatol. 2018;1(46):45-49. Romanian.
10. Donos N, Dereka X, Mardas N. Experimental models for guided bone regeneration in healthy and medically compromised conditions. Periodontal 2000. 2015 Jun;68(1):99-121. doi: 10.1111/prd.12077.
11. Sirbu D, Topalo V, Voloc A, Corcimari E, Voloc C. Studiul radiologic al osteoporozei la pacientii de sex feminin cu reabilitare implanto-protetica
la mandibulä [Radiological study of osteoporosis in female patients with rehabilitation for mandibular implant prosthesis]. Mold J Health Sci. 2018;1(15):44-55. Romanian.
12. Mofid MM, Inoue N, Atabey A, Marti G, Chao EYS, Manson PN, Vander Kolk CA. Callus stimulation in distraction osteogenesis. Plast Reconstr Surg. 2002 Apr;109(5):1621-1629. doi: 10.1097/00006534-20020415000020.
13. Erdogan O, Shafer DM, Taxel P, Freilich MA. A review of the association between osteoporosis and alveolar ridge augmentation. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007 Dec;104(6):738.e1-738.e13. doi: 10.1016/j.tripleo.2007.04.008.
14. Greenspan SL, Emkey RD, Bone HG, Weiss SR, Bell NH, Downs RW, McKeever C, Miller SS, Davidson M, Bolognese MA, Mulloy AL, Heyden N, Wu M, Kaur A, Lombardi A. Significant differential effects of alen-dronate, estrogen or combination therapy on the rate of bone loss after discontinuation of treatment of postmenopausal osteoporosis. A randomized, double-blind, placebo-controlled trial. Ann Intern Med. 2002 Dec 3;137(11):875-883. doi: 10.7326/0003-4819-137-11-200212030-00008.
15. Fini M, Giavaresi G, Torricelli P, Borsari V, Giardino R, Nicolini A, Carpi A. Osteoporosis and biomaterial osteointegration. Biomed Pharmaco-ther. 2004 Nov;58(9):487-493. doi: 10.1016/j.biopha.2004.08.016.
16. Marx RE, Sawatari Y, Fortin M, Broumand V. Bisphosphonate-induced exposed bone (osteonecrosis/ osteopetrosis) of the jaws: risk factors, recognition, prevention and treatment. J Oral Maxillofac Surg. 2005 Nov;63(11):1567-1575. doi: 10.1016/j.joms.2005.07.010.
17. Radzichevici M. Osteomielita toxica a maxilarelor, particularitätile clinice si paraclinice, metode de tratament [Toxic osteomyelitis of the maxilla, clinical and paraclinical features, treatment plan]. Med Stomatol. 2019;4(53):110-114. Romanian.
18. McCabe LR. Understanding the pathology and mechanisms of type I diabetic bone loss. J Cell Biochem. 2007 Dec 15;102(6):1343-1357. doi: 10.1002/jcb.21573.
19. Chatzopoulos GS, Cisneros A, Sanchez M, Wolff LF. Systemic medical conditions and periodontal status in older individuals. Spec Care Dentist. 2018 Nov;38(6):373-381. doi: 10.1111/scd.12319.
20. Gungor T, Hedlund T, Hulth A, Johnell O. The effect of irradiation on osteoclasts with or without transplantation of hematopoietic cells. Acta Orthop Scand. 1982;53(3):333-337. doi: 10.3109/17453678208992225.
21. Lerouxel E, Moreau A, Bouler JM, Giumelli B, Daculsi G, Weiss P, Malard O. Effects of high doses of ionising radiation on bone in rats: a new model for evaluation of bone engineering. Br J Oral Maxillofac Surg. 2009 Dec;47(8):602-607. doi: 10.1016/j.bjoms.2008.12.011.
22. Sciubba JJ, Goldenberg D. Oral complications of radiotherapy. Lancet Oncol. 2006 Feb;7(2):175-183. doi: 10.1016/S1470-2045(06)70580-0.
23. Song JY, Kim HH, Cho EJ, Kim TY. The relationship between gastroesophageal reflux disease and chronic periodontitis. Gut Liver. 2014;8(1):35-40. doi: 10.5009/gnl.2014.8.1.35.
24. Hirotomi T, Yoshihara A, Ogawa H, Ito K, Igarashi A, Miyazaki H. Salivary spinability and periodontal disease progression in an elderly population. Arch Oral Biol. 2008;53(11):1071-76. doi: 10.1016/j.archo-ralbio.2008.05.009.
25. Adachi K, Mishiro T, Tanaka S, Yoshikawa H, Kinoshita Y. A study on the relationship between reflux esophagitis and periodontitis. Intern Med. 2016;55(18):2523-2528. doi: 10.2169/internalmedicine.55.6898.
26. Martinez-Gimeno C, Acero-Sanz J, Martin-Sastre R, Navarro-Vila C. Maxillofacial trauma: influence of HIV infection. J Craniomaxillofac Surg. 1992 Oct;20(7):297-302. doi: 10.1016/s1010-5182(05)80399-3.
27. Campo J, Cano J, Romero J, Hernando V, Rodriguez C, Bascones A. Oral complication risks after invasive and non-invasive dental procedures in HIV-positive patients. Oral Dis. 2007;13(1):110-116. doi: 10.1111/j.1601-0825.2006.01262.x.
28. Noda K, Arakawa H, Kimura-Ono A, Yamazaki S, Hara ES, Maekawa K, Matsuka Y. A longitudinal retrospective study of the analysis of the risk factors of implant failure by the application of generalized estimating equations. J Prosthodont Res. 2015 Jul;59(3):178-184. doi: 10.1016/j. jpor.2015.04.003.
29. Bashutski J, Oh TJ, Chan HL, Wang HL. Guided tissue regeneration: a decision-making model. J Int Acad Periodontol. 2011 Jul;13(2):48-57.
30. Hyo-Jung L, Young-Kyun K, Jin-Young P, Su-Gwan K, Myung-Jin K, Pil-Young Y. Short-term clinical retrospective study of implants in geriatric patients older than 70 years. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2010 Oct;110(4):442-446. doi: 10.1016/j.tripleo.2010.02.019.
Author's ORCID iD and academic degrees
Alexandru Ghetiu, MD, PhD Applicant - https://orcid.org/0000-0003-1950-2871 Author's contribution
AG conceptualized the idea, conducted literature review, wrote the manuscript, revised and finalized the text. Funding
The trial was the author's initiative. The author is independent and takes responsibility for the integrity of the data and accuracy of the data analysis.
Ethics approval and consent to participate
The research project was approved by the Research Ethics Committee of Nicolae Testemitanu State University of Medicine and Pharmacy (Protocol No 8, 31.05. 2021).
Conflict of Interests
No competing interests were disclosed.