ISSN: 2455-5479
Archives of Community Medicine and Public Health
Case Report       Open Access      Peer-Reviewed

Medication-related osteonecrosis of the jaw-A case report and literature review

Chieh Chen1* and Da-Ming Liao2

1Division of Family Medicine, Hualien Armed Forces General Hospital, R.O.C, Taiwan
2Dental Department, Puli Christian Hospital, R.O.C, Taiwan
*Corresponding author: Chieh Chen, Division of Family Medicine, Hualien Armed Forces General Hospital, R.O.C, 970 No. 198, Minde 1st Street, Hualien City, Taiwan, Tel: 0928-698950; E-mail: guppy5230@yahoo.com.tw
Received: 09 February, 2023 | Accepted: 20 February, 2023 | Published: 21 February, 2023
Keywords: Fracture prevention; Osteoporosis; Medication-related osteonecrosis of the jaw; Bone anti-resorptive agent; Osteonecrosis of the jaw

Cite this as

Chen C, Da-Ming L (2023) Medication-related osteonecrosis of the jaw-A case report and literature review. Arch Community Med Public Health 9(1): 016-021. DOI: 10.17352/2455-5479.000196

Copyright License

© 2023 Chen C, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Osteoporosis is a skeletal disease caused by changes in the structure of the human skeleton, resulting in fragile and easily fractured bones. Because it is more common in postmenopausal women or the elderly, fractures may cause disability in the elderly, resulting in reduced quality of life, bedridden, or increased mortality. Therefore, the treatment of osteoporosis is one of the important issues in today’s aging society. In addition, diseases such as bone metastasis of cancer and multiple myeloma also need to be paid attention to. Drugs for the treatment of osteoporosis have been widely used in the prevention and treatment of osteoporosis because of their inhibitory effect on osteoclast activity, and even become the first-choice drug for bone metastases of some malignant tumors. Drugs for the treatment or prevention of osteoporosis can inhibit osteoclasts, and can also be used to treat hypercalcemia complications of malignant tumors or bone-related systemic diseases. For example, bisphosphonates or monoclonal antibody preparations (eg: Denosumab, Romosozumab, etc.) can resist bone resorption. However, in recent years, the literature pointed out that patients using anti-bone resorption drugs may have adverse reactions to maxillofacial osteonecrosis. Medication-Related Osteonecrosis of the Jaw (MRONJ) may occur in patients with osteoporosis and tumors. Bisphosphonates or synthetic human monoclonal antibodies can inhibit bone resorption and are currently the most commonly used drugs for the treatment of osteoporosis in the world. The literature for nearly 20 years has shown that long-term use of such antiresorptive drugs increases the risk of osteonecrosis of the jaw in the oral cavity. Therefore, MRONJ is still a complication that we must pay attention to. Once MRONJ occurs, it is recommended to refer to an oral surgeon immediately; the current clinical treatment methods include the use of antibacterial mouthwash and drugs to control pain in mild cases, and antibiotics for infection control in moderate cases.

Introduction

Osteoporosis is defined as low bone mineral density caused by altered bone microstructure, ultimately predisposing patients to low-impact, fragility fractures. Osteoporotic fractures lead to a significant decrease in quality of life, with increased morbidity, mortality, and disability. Medication-Related Osteonecrosis of the Jaw (MRONJ) is a rare, severe debilitating condition from unknown causes. It is characterized by nonhealing exposed bone in a patient with a history of antiresorptive or antiangiogenic agents in the absence of radiation exposure to the head and neck region. Osteonecrosis of the jaw is a poorly understood condition that has recently been associated with the use of potent bisphosphonate treatment. The prevalence appears to be approximately 1% - 10% in patients with malignancy treated with very high doses of intravenous bisphosphonates. The use of high-dose corticosteroids, such as prednisone, is a common cause of avascular necrosis. The reason is unknown, but some experts believe that corticosteroids can increase lipid levels in the blood, reducing blood flow. The people at highest risk for ONJ in patients taking bisphosphonates are people who have cancer that has spread to the bones and are being treated with intravenous bisphosphonates zoledronic acid or pamidronate. The people at the highest risk had also had dental procedures such as tooth extractions. There are more and more older people in Taiwan. Presently, nearly one-fifth of the elderly population (the elderly are defined as those over 65 years old), so the future public health policy will focus on the care of the elderly and the prevention of diseases of older age. Among many senile diseases, osteoporosis has been a concern. Osteoporosis is a skeletal disease in which bones are fragile and prone to fractures due to changes in the structure of the human body. Osteoporosis tends to occur in menopausal women and the elderly population; then resulting fractures most commonly occur in the spine, hip, and distal radius of the wrist. Fractures can be disabling and lead to poor quality of life, such as bedridden or increased mortality in the elderly. Therefore, the treatment of osteoporosis is one of the important issues in today’s aged society. Osteoporosis is a common skeletal metabolic disease in older people. It can cause persistent bone density loss, bone fragility and low Bone Mineral Density (BMD), so it is easy to cause non-traumatic fractures [1].

Case

A 42-year-old woman, five months after receiving regular chemotherapy for stage IV breast cancer, found bone metastases due to nuclear medicine scans and used Denosumab (Prolia) subcutaneous injection to relieve the discomfort of the bone pain. When she went to the dental clinic for her gum inflammation, Dr. Liao found that there was osteonecrosis of the mandible (Figures 1,2).

Discussion

Definition of MRONJ

The latest definition of Medication-Related Osteonecrosis of the Jaw [2] is a consensus issue by the American Academy of Oral and Maxillofacial Surgery in 2022. The diagnosis of this type of disease must meet the following three items:

  1. Current or previous treatment with antiresorptive therapy alone or in combination with immune modulators or anti-angiogenesis drugs.
  2. Exposed bone or bone that can be probed through an intraoral or extraoral fistula in the maxillofacial region that has persisted for more than 8 weeks. Internal and external fistulas protrude to the surface of the bone and persist for more than eight weeks.
  3. No history of radiation therapy to the jaws or metastatic disease to the jaws. (No history of radiation therapy to the jaws or metastatic disease to the jaws).
Incidence rate

The proportion of MRONJ due to the use of drugs in the world is relatively small, but it is still listed as a common adverse reaction of antiresorptive drugs [3]. Among patients with osteonecrosis of the jaw, its pathogenic mechanism has not been fully elucidated; however, since Marx et al. published 36 cases in 2003, osteonecrosis of the jaw occurred mainly due to long-term use of bisphosphonates [4]. According to the data of the American Society of Oral and Maxillofacial Surgery in 2022, the risk of osteoporosis patients getting MRONJ is less than 0.05%; the risk of malignant tumors is higher, less than 5%. In patients with osteoporosis, the incidence of osteonecrosis of the jaw after injection of denosumab will increase (0.04% - 0.3%), while those using bisphosphonates will have a lower risk (0.02% - 0.05%). Many articles that report in the world pointed out that, the incidence of MRONJ was 0.283% per year in patients treated with osteoporosis using oral BPs (bisphosphonate such as alendronate), but the incidence of MRONJ increased to 0.92% in the tenth year [5,6]. Taiwan’s data shows that MRONJ the average age is 73 years old, and 3/4 were women. Therefore, it is necessary to educate patients to monitor themselves before using drugs and ask patients to inform the dentist before tooth extraction.

Pathophysiological mechanism

The process of bone metabolism starts with osteoclasts contacting the bone surface and decomposing the bone matrix. During the process of the bone matrix being decomposed, growth factors are released at the same time to stimulate the formation of osteoblasts, which then form mature bones. Rizzoli [4] put forward a theory in 2008, stating that the pathological causes of delayed jawbone healing caused by bisphosphonates include: 1. Affecting angiogenesis. 2. Affect bone metabolism, 3. Inflammation, trauma, and oral surgery. When bisphosphonates are attached to the bone tissue and then absorbed by osteophagocytic cells, they inhibit the development of osteophagic cells by stimulating the release of osteophagic inhibitory molecules, indirectly causing the self-apoptosis of osteophagic cells and inhibiting bone regeneration and re-absorption. Once bisphosphonates are combined with bones, they are difficult to be metabolized by the human body and will be attached to bones for a long time. Taking alendronate as an example, the half-life in bones exceeds ten years. Both denosumab and romosozumab are human monoclonal antibodies that can be used in patients with osteoporosis, but their mechanism of action is different. Denosumab is a receptor activator of nuclear factor kappa-B ligand (RANK-L) inhibitor, which can inhibit osteoclasts. It has a short half-life and its efficacy will disappear six months after injection. Romosozumab regulates the Wnt pathway and combines with sclerostin to increase bone formation and reduce bone resorption [7]. The treatment of osteoporosis relies on inhibiting the activity of osteoclasts, but over-inhibition of the activity of osteoclasts may lead to excessive accumulation of inactive bone cells, causing continuous micro-trauma to the bones and increasing the probability of osteonecrosis of the jaw [8,9]. Bone resorption drugs enter the human body and hinder the progress of osteoclasts [2], when the dead bone cells cannot be decomposed and release the growth factors contained in the cells, the osteogenesis cannot proceed, and the dead bone cannot be replaced by new bone cells. Drugs that inhibit bone resorption can also cause jaw bone ischemia, immune dysfunction, and poor oral hygiene, followed by secondary infections, which become the type of osteomyelitis MRONJ. Clinical symptoms include pain, infection, and poor oral hygiene (Figure 3) [10-12]. Because the jawbone has a faster rate of bone turnover than other bones, the jawbone will be affected more [13,14]. If bone necrosis occurs in the jawbone, the gum soft tissue attached to the necrotic jawbone will also be necrotic. Especially in elderly patients, carrion will be found in the oral cavity, and the exposed area will also be due to traumatic fractures of the jawbone, tooth extraction, and inappropriate activities. Factors such as dentures, severe periodontal diseases, or oral infections caused by deep caries, become more serious. Other non-specific symptoms are mostly gingival inflammation, swelling, suppuration, bleeding, loose teeth, unhealed wounds, numbness of the jawbone, exposed alveolar, bone resorption, bone sclerosis, moth-eaten and Rotten bones spawn.

Risk factors of MRONJ

The risk factors for medication-related osteonecrosis of the jaw are drugs that inhibit bone resorption; in addition, other causes that make MRONJ more likely to occur are considered to be called initiating factors [15], such as the patient’s own chronic systemic diseases, inflammatory conditions of the jaw itself, etc. Discussion of risk factors is mainly divided into three categories for discussion [16], 1. Drug-related factors and their indications; 2. Local factors; 3. Systemic factors.

1. Drug-related factors: Drug-related factors include dose, dosage form, potency, or duration of use. Among osteoporosis patients, the incidence rate of patients who use oral bisphosphonates is about 0.05%; the incidence rate of patients who use Denosumab (DMB) is about 0.3% in ten years; but cancer patients will use more doses than osteoporosis patients. The probability of producing MRONJ will increase to 0.03% - 5%. Osteonecrosis occurred in 0% - 0.15% of patients with osteoporosis and 1% in DMB patients who received bisphosphonates for jawbone-related surgery. In cancer patients, the rate ranged from 1.6% - 14.8%; while the proportion of cancer patients with MRONJ is higher, obviously the influence of drug dose is huge. In addition, the duration of drug use will also affect. Generally using bisphosphonate or DMB in patients with malignant tumors increases, and the incidence of MRONJ is higher. Among osteoporosis patients, bisphosphonate for four years or more is even a 0.21% chance that users will have MRONJ.

2. Local factors: Since the bone turnover rate of the jawbone is several times that of the long bones [14,16], MRONJ mainly presents oral-related symptoms, and patients often suffer from oral alveolar bone disease, surgery, or trauma. For example, Osteonecrosis of the jaw occurs only from local infections, tooth extractions, implants, wounds, or pressure sores caused by improperly fitted dentures. Therefore, dental treatments such as tooth extractions will be considered the most important risk factors in the study. However, the cause-and-effect relationship is also because the alveolar bone wounds in the oral cavity are easily affected by anti-resorptive drugs, resulting in slower healing, infection, and even osteonecrosis. Alveolar bone surgery is still listed as a relevant local factor in the current literature, and the mandibular bone accounts for 75% of the jawbone, which is the most prone location for MRONJ. If there are exostoses in the jawbone or the alveolar ridge behind the mandible, there are more chances of ulceration due to the pressure of the dentures or the thinner mucosa, which in turn increases the chance of osteonecrosis [17]. The original inflammation in the oral cavity can also cause MRONJ. Before taking anti-resorptive drugs or such drugs, the inflammation in the teeth, including periodontitis or periapical inflammation, etc., or the bone caused by abnormal occlusion. Injuries can also increase the probability of osteonecrosis. Studies have also found that dental examination and treatment before treatment can significantly reduce the occurrence of MRONJ [16].

3. Systemic factors: Many systemic or demographic risk factors, including age, postmenopausal women, patients on long-term systemic steroid therapy, cancer, anemia, diabetes mellitus, hyperparathyroidism, rheumatoid arthritis, low serum calcium level, etc., and even smokers, etc. Since anti-resorptive agents are often used by female cancer patients and osteoporosis patients, chronic diseases and bad living habits, such as diabetes and smoking, will affect peripheral blood supply and affect wound healing, but whether it is direct risk factors are still inconclusive [2,16].

Timing of referral for medication-related osteonecrosis of the jaw

After long-term use of anti-resorptive drugs, various symptoms of MRONJ may appear, including gingival or oral mucosa rupture, redness, swelling and pain of the gums, increased shaking of the teeth around the affected area; in addition to the exposure of the alveolar bone, sometimes the surrounding soft tissues inflammation and swelling, suppuration and infection may occur. If the mandibular bone lesion affects the inferior alveolar nerve, there will be numbness of the lips; the maxillary bone lesion may cause the mouth, nose, and sinuses to communicate and sinusitis. If you have the above symptoms, you should immediately refer to an oral surgeon. If you need dental surgery, you must arrange a return visit every six to eight weeks to ensure the successful healing of the gingival mucosa [12,14,16,18,19]. In 1994, the World Health Organization evaluated osteoporosis and recommended that the bone density value be used as the diagnostic standard. The bone density value of any bone in the body is lower than -2.5 standard deviations of the average value of 20-year-old young women (T-score is less than -2.5) can be diagnosed as osteoporosis. If combined with fractures, it is called severe osteoporosis; the bone density value is between -1 and -2.5 standard deviations (T-score is between -1 and -2.5), then called osteopenia, bone density value higher than -1 standard deviation (T-score greater than -1) is normal. Drugs for the treatment or prevention of osteoporosis can inhibit osteoclasts, and can also be used to treat hypercalcemia complications of malignant tumors or bone-related systemic diseases, such as bisphosphonates (BPs) (Table 1) or monoclonal antibody preparations such as Denosumab (DMB), Romosozumab, etc., can resist bone resorption; however, recent literature has pointed out that patients who use anti-resorptive drugs may have adverse reactions of maxillofacial osteonecrosis [1] and this adverse reaction is currently often known as medication-related osteonecrosis of the jaw (MRONJ), or it used to be called bisphosphonate-related osteonecrosis of the jaw (BRONJ). Since the American Association of Oral and Maxillofacial Surgeons (AAOMS) published a consensus document in 2007, it was updated in 2009, 2014, and 2022 in order to spread the knowledge and experience development of MRONJ. The American Academy of Oral and Maxillofacial Surgeons believes that physicians should be familiar with the adverse side effects of MRONJ associated with anti-resorptive or anti-angiogenic drugs; dentists treat patients with risky drugs such as osteoporosis, multiple sclerosis, rheumatoid arthritis, multiple myeloma, or patients with bone metastases of cancer, special caution should be exercised.

Clinical treatment and prevention strategies

The best way to reduce MRONJ is to prevent it. The public should go to the dentist every six months to reduce the occurrence of tooth decay and periodontal disease [12,18]. During the period of medication, good oral hygiene should be maintained. For discomfort symptoms and oral health, you should take the initiative to inform the dentist about the history of osteoporosis, cancer, or tumor-related medication, such as bisphosphonates, steroids, etc. When doing invasive dental treatment, and fully communicating with the dentist to understand the incidence of osteonecrosis of the jaw and preventive methods; physicians need to be more cautious before prescribing anti-resorptive drugs. It is recommended to consult an oral surgeon or dentist to evaluate the oral condition. Complete caries filling, root canal treatment, and periodontal disease treatment to reduce the chance of osteonecrosis of the jaw. Table 2 shows the prevention strategies recommended by the American Academy of Oral and Maxillofacial Surgeons in 2022. Once MRONJ occurs, referral to an oral surgeon is recommended (Table 2). The current clinical treatment methods are to use an antibacterial mouthwash and drugs to control pain in mild cases, and antibiotics to control infection in moderate cases [19], supplemented by conservative bone decay surgery. If severe osteonecrosis occurs, large-scale surgery will be performed. Extensive bone debridement surgery, even jawbone resection, and reconstruction; the use of hyperbaric oxygen therapy (HBO) is still controversial. There are reports that hyperbaric oxygen combined with drug withdrawal can significantly and continuously relieve the effect. In addition, after using hyperbaric oxygen, most patients have a short-term remission Phenomenon, but easy to relapse.

Conclusion

As defined by the World Health Organization (WHO), osteoporosis is present when BMD is 2.5 SD or more below the average value for young healthy women (a T-score of < −2.5 SD). A second, higher threshold describes “low bone mass” or osteopenia as a T-score that lies between −1 and −2.5 SD. Bone density measurement by DXA at the hip and spine is generally considered the most reliable way to diagnose osteoporosis and predict fracture risk. Some people have a peripheral DXA, which measures bone density in the wrist and heel. This type of DXA is portable and may make it easier for screening. Osteoporosis is a health condition that weakens bones, making them fragile and more likely to break. It develops slowly over several years and is often only diagnosed when a fall or sudden impact causes a bone to break (fracture). A condition in which there is a decrease in the amount and thickness of bone tissue. This causes the bones to become weak and break more easily. Eating habits: You are more likely to develop osteoporosis if your body doesn’t have enough calcium and vitamin D. Although eating disorders like bulimia or anorexia are risk factors, they can be treated. Lifestyle: People who lead sedentary (inactive) lifestyles have a higher risk of osteoporosis. Drugs for the treatment or prevention of osteoporosis can inhibit osteoclasts, and can also be used to treat hypercalcemia complications of malignant tumors or bone-related systemic diseases, such as bisphosphonates or monoclonal antibody preparations (such as Denosumab, Romosozumab, etc.) can resist bone resorption; however, recent literature has pointed out that patients who use anti-resorptive drugs may have adverse reactions of maxillofacial osteonecrosis; bisphosphonates can inhibit bone resorption. At present, it is one of the most commonly used drugs for the treatment of osteoporosis in the world, but many case reports have presented more and more evidence that long-term use of bisphosphonates increases the risk of adverse reactions of oral severe osteonecrosis of the jaw. In addition, osteoporosis drugs that may cause osteonecrosis of the jaw to include 1. The incidence of bisphosphonates such as oral Alendronate is about 0.004-0.1%, and intravenous Zoledronate is about 0.017%. Generally, oral drugs have a lower incidence of jaw osteonecrosis than injection drugs; 2. The incidence rate of Denosumab synthetic human monoclonal antibody (Prolia™) was 0.04%. Anti-resorptive drugs can reduce the incidence of fractures caused by osteoporosis, and can also treat cancer bone metastases and multiple myeloma, etc. [20]. But before using these agents, patients and their families must be informed of the risk of osteonecrosis of the jaw, and patients should be advised not to treat osteoporosis. In addition to caring for cancer and tumors, the health of the oral cavity and jawbone must also be taken care of. In addition, all specialists need to work together to formulate an appropriate treatment plan based on each patient’s different diseases and medication methods, in order to effectively reduce the occurrence of MRONJ.

  1. Aguirre JI, Castillo EJ, Kimmel DB. Biologic and pathologic aspects of osteocytes in the setting of medication-related osteonecrosis of the jaw (MRONJ). Bone. 2021 Dec;153:116168. doi: 10.1016/j.bone.2021.116168. Epub 2021 Sep 3. PMID: 34487892; PMCID: PMC8478908.
  2. Ruggiero SL, Dodson TB, Aghaloo T, Carlson ER, Ward BB, Kademani D. American Association of Oral and Maxillofacial Surgeons' Position Paper on Medication-Related Osteonecrosis of the Jaws-2022 Update. J Oral Maxillofac Surg. 2022 May;80(5):920-943. doi: 10.1016/j.joms.2022.02.008. Epub 2022 Feb 21. PMID: 35300956.
  3. Marx RE. Pamidronate (Aredia) and zoledronate (Zometa) induced avascular necrosis of the jaws: a growing epidemic. J Oral Maxillofac Surg. 2003 Sep;61(9):1115-7. doi: 10.1016/s0278-2391(03)00720-1. PMID: 12966493.
  4. Rizzoli R, Burlet N, Cahall D, Delmas PD, Eriksen EF, Felsenberg D, Grbic J, Jontell M, Landesberg R, Laslop A, Wollenhaupt M, Papapoulos S, Sezer O, Sprafka M, Reginster JY. Osteonecrosis of the jaw and bisphosphonate treatment for osteoporosis. Bone. 2008 May;42(5):841-7. doi: 10.1016/j.bone.2008.01.003. Epub 2008 Jan 18. PMID: 18314405.
  5. Chiu WY, Chien JY, Yang WS, Juang JM, Lee JJ, Tsai KS. The risk of osteonecrosis of the jaws in Taiwanese osteoporotic patients treated with oral alendronate or raloxifene. J Clin Endocrinol Metab. 2014 Aug;99(8):2729-35. doi: 10.1210/jc.2013-4119. Epub 2014 Apr 23. PMID: 24758181.
  6. Aguirre JI, Castillo EJ, Kimmel DB. Preclinical models of medication-related osteonecrosis of the jaw (MRONJ). Bone. 2021 Dec;153:116184. doi: 10.1016/j.bone.2021.116184. Epub 2021 Sep 11. PMID: 34520898; PMCID: PMC8743993.
  7. Marx RE. Understanding Drug-Induced Osteonecrosis of the Jaws. In: Drug-Induced Osteonecrosis of the Jaws: How to Diagnose, Prevent, and Treat It. 1st ed. Quintessence Publishing. 2022: 3–8.
  8. Dunphy L, Salzano G, Gerber B, Graystone J. Medication-related osteonecrosis (MRONJ) of the mandible and maxilla. BMJ Case Rep. 2020 Jan 5;13(1):e224455. doi: 10.1136/bcr-2018-224455. Corrected and republished in: Drug Ther Bull. 2020 Nov;58(11):172-175. PMID: 31907213; PMCID: PMC6954753.
  9. Allen MR, Burr DB. The pathogenesis of bisphosphonate-related osteonecrosis of the jaw: so many hypotheses, so few data. J Oral Maxillofac Surg. 2009 May;67(5 Suppl):61-70. doi: 10.1016/j.joms.2009.01.007. PMID: 19371816.
  10. AlDhalaan NA, BaQais A, Al-Omar A. Medication-related Osteonecrosis of the Jaw: A Review. Cureus. 2020 Feb 10;12(2):e6944. doi: 10.7759/cureus.6944. PMID: 32190495; PMCID: PMC7067354.
  11. Kishimoto H, Noguchi K, Takaoka K. Novel insight into the management of bisphosphonate-related osteonecrosis of the jaw (BRONJ). Jpn Dent Sci Rev. 2019 Nov;55(1):95-102. doi: 10.1016/j.jdsr.2018.09.002. Epub 2019 May 17. PMID: 31193410; PMCID: PMC6526304.
  12. Ruggiero SL, Dodson TB, Fantasia J, Goodday R, Aghaloo T, Mehrotra B, O'Ryan F; American Association of Oral and Maxillofacial Surgeons. American Association of Oral and Maxillofacial Surgeons position paper on medication-related osteonecrosis of the jaw--2014 update. J Oral Maxillofac Surg. 2014 Oct;72(10):1938-56. doi: 10.1016/j.joms.2014.04.031. Epub 2014 May 5. Erratum in: J Oral Maxillofac Surg. 2015 Jul;73(7):1440. Erratum in: J Oral Maxillofac Surg. 2015 Sep;73(9):1879. PMID: 25234529.
  13. Soutome S, Otsuru M, Hayashida S, Murata M, Yanamoto S, Sawada S, Kojima Y, Funahara M, Iwai H, Umeda M, Saito T. Relationship between tooth extraction and development of medication-related osteonecrosis of the jaw in cancer patients. Sci Rep. 2021 Aug 26;11(1):17226. doi: 10.1038/s41598-021-96480-8. PMID: 34446755; PMCID: PMC8390686.
  14. Dixon RB, Tricker ND, Geretto LP: Bone turnover in early canine mandible and tibia. J Dent Res. 1997; 76: 336.
  15. Kwon TG. Risk Factors for Medication-Related Osteonecrosis of the Jaw. In: Medication-related osteonecrosis of the jaws. Bisphosphonates, Denosumab, and New Agents Springer Publishing. 2015; 32-3.
  16. Nicolatou-Galitis O, Schiødt M, Mendes RA, Ripamonti C, Hope S, Drudge-Coates L, Niepel D, Van den Wyngaert T. Medication-related osteonecrosis of the jaw: definition and best practice for prevention, diagnosis, and treatment. Oral Surg Oral Med Oral Pathol Oral Radiol. 2019 Feb;127(2):117-135. doi: 10.1016/j.oooo.2018.09.008. Epub 2018 Oct 9. PMID: 30393090.
  17. Fliefel R, Tröltzsch M, Kühnisch J, Ehrenfeld M, Otto S. Treatment strategies and outcomes of bisphosphonate-related osteonecrosis of the jaw (BRONJ) with characterization of patients: a systematic review. Int J Oral Maxillofac Surg. 2015 May;44(5):568-85. doi: 10.1016/j.ijom.2015.01.026. Epub 2015 Feb 26. PMID: 25726090.
  18. Kuroshima S, Sasaki M, Sawase T. Medication-related osteonecrosis of the jaw: A literature review. J Oral Biosci. 2019 Jun;61(2):99-104. doi: 10.1016/j.job.2019.03.005. Epub 2019 May 15. PMID: 31109863.
  19. Querrer R, Ferrare N, Melo N, Stefani CM, Dos Reis PED, Mesquita CRM, Borges GA, Leite AF, Figueiredo PT. Differences between bisphosphonate-related and denosumab-related osteonecrosis of the jaws: a systematic review. Support Care Cancer. 2021 Jun;29(6):2811-2820. doi: 10.1007/s00520-020-05855-6. Epub 2020 Nov 2. Erratum in: Support Care Cancer. 2021 Mar 18;: PMID: 33140246.
  20. Yao S, Ding X, Rong G, Zhou J, Zhang B. Association Between Malignant Diseases and Medication-Related Osteonecrosis of the Jaw (MRONJ): A Systematic Review and Meta-Analysis. J Craniofac Surg. 2022 Oct 3. doi: 10.1097/SCS.0000000000009033. Epub ahead of print. PMID: 36184756.
 

Help ?