|Year : 2019 | Volume
| Issue : 2 | Page : 93-100
Clinical utility of hyperbaric oxygen therapy in dentistry
Kaitlyn Re1, Shrey Patel1, Jason Gandhi2, Yiji Suh1, Inefta Reid3, Gunjan Joshi3, Noel L Smith4, Sardar Ali Khan5
1 Department of Physiology and Biophysics, Stony Brook University School of Medicine, Stony Brook, NY, USA
2 Department of Physiology and Biophysics, Stony Brook University School of Medicine, Stony Brook, NY, USA; Medical Student Research Institute, St. George's University School of Medicine, Grenada, West Indies
3 Department of Internal Medicine, Stony Brook Southampton Hospital, Southampton, NY, USA
4 Foley Plaza Medical, New York, NY, USA
5 Department of Physiology and Biophysics; Department of Urology, Stony Brook University School of Medicine, Stony Brook, NY, USA
|Date of Submission||20-Feb-2019|
|Date of Acceptance||16-Apr-2019|
|Date of Web Publication||25-Jun-2019|
Sardar Ali Khan
Department of Physiology and Biophysics; Department of Urology, Stony Brook University School of Medicine, Stony Brook, NY
Source of Support: None, Conflict of Interest: None
This fuller impact of the use of hyperbaric oxygen therapy within dentistry is taking greater notice with newer research findings. There are new advancements in research regarding postradiotherapy cases, osteonecrosis of the jaw, osteomyelitis, periodontal disease, and dental implants. Hyperbaric oxygen therapy can even be used in conjunction with other procedures such as bone grafting. Although the research and clinical utility has come a long way, there are several complications to be mindful of during the application of hyperbaric oxygen therapy.
Keywords: hyperbaric oxygen therapy; dentistry; osteoradionecrosis of the jaw; dental implants; periodontal disease; oral submucous fibrosis; mandibular osteomyelitis
|How to cite this article:|
Re K, Patel S, Gandhi J, Suh Y, Reid I, Joshi G, Smith NL, Khan SA. Clinical utility of hyperbaric oxygen therapy in dentistry. Med Gas Res 2019;9:93-100
|How to cite this URL:|
Re K, Patel S, Gandhi J, Suh Y, Reid I, Joshi G, Smith NL, Khan SA. Clinical utility of hyperbaric oxygen therapy in dentistry. Med Gas Res [serial online] 2019 [cited 2019 Sep 16];9:93-100. Available from: http://www.medgasres.com/text.asp?2019/9/2/93/260651
| Introduction|| |
Hyperbaric oxygen therapy (HBOT) facilitates the transfer of oxygen to the tissues of the human body. By doing so, it promotes healing of wounds and minimizes the typical recovery time for patients. At this juncture, strictly within dental medicine, HBOT indicates the distribution of comprehensive oxygen at pressures greater than 1.4 atmosphere absolute (ATA), often in a series of treatments. This treatment requires the patient to stand within a hyperbaric chamber with pressure greater than ambient. It has many uses such as patient care, and wound care within standard medicine and dental medicine.
HBOT exploits numerous physiological principles of how gases and oxygen react under specific adjustments of pressure. There is a direct relationship between the concentration of oxygen in solution and the diffusion gradient. The increase in concentration of oxygen in solution results in the increase of the diffusion gradient for the delivery into deeper tissue, thus being the basis for HBOT. Henry’s law defines that at constant temperature, the concentration of gas that is dissolved in a given liquid is proportional to the partial pressure of the gas above the fluid. In HBOT, the oxygen level is amplified, which highly increases the oxygen tension in the tissues. When the treatment is concluded, the oxygen tension decreases allowing for an inundation of neutrophils. Neutrophils are a type of white blood cells which specifically aid in fighting off infection and tissue regrowth. Conclusively, the increase in dissolved oxygen generated by HBOT has potential to alter tissue responses to disease and injury. In some cases, this may prevent death and or amputation of limbs. HBOT is most commonly executed at a compression rate of 0.067 ATA/min (6.8 kPa/min). However, a study conducted in 2007 concluded that the pressure equalization can lead to middle ear pain and or discomfort, cranial sinus pain, and teeth pain. It is recommended that specific care must be implemented with patients who suffer from peripheral circulatory disorders and have short interval between clinical symptoms, as per Hirsch and Watson and the American College of Cardiology/American Heart Association guidelines.
| History|| |
The use of HBOT can be dated back to the 1600s; however it was unverified until 1956. Ite Boerema, the chief of surgery at University of Amsterdam, The Netherlands is known for his success while using HBOT to lengthen safe operating times during cardiac surgery. By 1960, records show that there was a drastic decrease in mortality rate from 66% to 23%. Records also indicate that HBOT excessively decreased the invalidity rate, which demonstrates its ability to save both life and limb.
HBOT utilizes several physiologic principles of how gases respond under pressure and more specifically of how oxygen responds under pressure. The increase in concentration of oxygen in solution, based on its solubility under pressure, raises the diffusion gradient for its delivery into deep tissues, which is the premise of HBOT. Ultimately the increases in dissolved oxygen generated by hyperbaric therapy have several physiologic effects that can alter tissue responses to disease and injury. As this technology becomes more available to clinical practice, HBOT should be considered as a therapeutic option.
The study of physiology under inflated pressures is said to have begun in 1644 by an Italian physicist Evangelista Torricelli, who invented the first barometer. The collaboration between Galileo, Blaise Pascal, Robert Boyle, and Robert Hooke lead to the discovery of the inverse relationship between pressure and altitude. Hooke is responsible for creating the first air pump that eventually helped facilitate the creation and discovery of HBOT.
| Therapeutic Principles|| |
The fundamental mechanism for HBOT depends on the intracellular inception of reactive species of oxygen and nitrogen. Cell signaling transduction cascades within this mechanism signify the importance of the reactive species, oxygen and nitrogen. The reactive species of oxygen and nitrogen work together to cause nitrative stress by damaging the cells.
| Uses in Dentistry|| |
While it has various uses specific to dental medicine, HBOT is most often used for prevention of complications during radiation therapy. It is known to effectively increase tissue oxygenation and, moreover, expedite the healing of wounds. The healing of wounds is especially significant in periodontal disease and oral submucous fibrosis. Recent studies on the role of HBOT in the management of necrotizing fasciitis, wound dehiscence after intraoral bone grafting in non-irradiated patients, osteoradionecrosis of the mandible, and oral submucous fibrosis are crucial for recognizing the future scope of impact HBOT in dentistry. In specific, necrotizing fasciitis is a flesh-eating disease, as the infection commonly leads to death of parts of the body’s soft tissue. This disease spreads rapidly and requires immediate aggressive surgical management and an extended debridement. In some cases, early amputation is required. Wound dehiscence, the separation of the edges of a surgical incision, requires the doctor to clean and debride the lesion to remove the dead and infected tissue, in which amplifies the healing process. The most important aspect of this is expediting the healing process in which prevents further complications such as surgical site infections. HBOT has the potential to prevent the following complications that co-inside with necrotizing fasciitis and wound dehiscence.
HBOT is an effective utilization in various chronic radiation-induced tissue injuries. Osteoradionecrosis prophylaxis resulting from a radiation-induced dental disease had an underlying response rate of 96%. The overall response rate for soft tissue necrosis and hemorrhagic cystitis was 84%. [Table 1] lists the use of HBOT in dental cases with respect to radiotherapy.
Osteoradionecrosis of the jaw is commonly acknowledged as death of the jaw bone and bone within the head and neck region because of the decreased oxygen tension-hypotension hypocellularity and hypovascularity. Osteoradionecrosis is a nonhealing, nonseptic lesion of the bone in which bone volume and density cannot be maintained by the hypocellular, hypovascular, hypoxic tissue, which cannot adequately meet its metabolic demands. As the soft tissue decays, the bone begins to become exposed. Saliva and other foreign entities within the oral cavity will prompt cross-contamination, thus leading to significance in infection and further complications. Symptoms of osteoradionecrosis include mouth pain, jaw swelling, poor smelling breath, mouth sores, and difficulty opening the jaw.,
In 2013, a study was done regarding HBOT and mandibular osteoradionecrosis during tooth extractions. It was determined that HBOT provided adequate prevention. HBOT in conjunction with penicillin proceeding tooth extraction proved to have a more efficient and longer lasting recovery in comparison to the patients exclusively treated with penicillin. Time sensitivity is imperative – if the treatment of HBOT is administered 2 weeks prior to the dental treatment, complications arise in 1.5% to 4.2% of the patients. If the treatment is prolonged to six months prior to the dental treatment, the percentage of complications increases to 15.8%. Osteoradionecrosis often yields an array of serious side effects. These include facial deformity, pain, pathological fracture, sequestration of devitalized bone, and orocutaneous fistulas. Dysgeusia, paresthesia, bone exposure, gingival ulceration, tooth fracture, pathologic mandibular fracture, xerostomia, and orocutaneous fistula are common within the oral cavity. All of the following induce extreme irritation and pain, and often lead to more severe complications if not treated in a timely manner. HBOT increases the oxygen tension in the region and promotes angiogenesis, the development of new blood cells. The development of new blood cells directly leads to wound healing. When a wound is beginning to heal, the angiogenic capillaries sprout and invade the fibrin-rich would clot. When the clot is invaded, the alpha v beta 3 receptors are targeted, which are necessary for wound healing.
Osteoradionecrosis is often diagnosed in three different stages: spontaneous, from trauma preceding radiotherapy, and due to trauma post-radiotherapy. In the spontaneous stage, the high dose of radiation during treatment can directly lead to death of the bone cells, destroying the bone. Radiation of > 700 cGy is considered enough to immediately kill the bone cells after one full year. In trauma preceding radiotherapy, if radiation therapy is within 21 days of a tooth extraction, often times this leads to radiotherapy for oral cancers or mandibulotomy. Trauma post-radiotherapy is very common, especially after dental extractions. Tooth extractions normally follow severe infection and inflammation of gum tissue surrounding the tooth. After a tooth is extracted, the tissues become 3-H with advancing years, typically 3. As the radiation affects progress, the tissue cannot handle the increase in vascular nutrition and oxygen demands that are required for healing. If the tissue cannot heal, osteoradionecrosis will develop.
A Marx protocol was created for the treatment of ORN within the jaw, that includes three critical stages. Stage I of this process requires setting the HBOT level to 2.4 ATA for a total of 90 minutes. After a third of the session is completed, it is necessary to inspect the targeted area for softening of exposed bone and granulation tissue. If the following are present, it is suggested to follow up with non-surgical debridement and follow up with an addition of 10 HBOT sessions. Stage II is necessary only if little or no response is observed after the previous 30 sessions of treatment. Stage II requires peripheral resection of non-vital bone to bleeding bone margins, followed by 10 postoperative sessions of HBOT. Stage III recommends resection of the mandible after 30 ineffective sessions of HBOT. Add plates and pins and covering the soft tissue deficit will help to stabilize the mandible. The 10 subsequent treatments of HBOT and 3 months of healing are recommended. At this point, bone remodeling can be completed.
Postradiation therapy can both improve quality of life and increase average life span of those suffering from post-radiation central nervous system injury. Various experiments have concluded that HBOT does in fact stimulate improvements in subjective, clinical, and radiological outcomes. Sometimes, radiation such as HBOT can bring upon xerostomia on those treated. Xerostomia is defined as dry mouth resulting from reduced or absent saliva flow. Radiation therapy, such as HBOT, often damages salivary glands while also treating the diagnosed issue. Radiation-induced xerostomia is one of the most common morbidities of radiation therapy in patients with head and neck cancer. The more important conclusion is that HBOT often helps to cure and heal those diagnosed with head and neck cancer, explaining why the xerostomia is often overlooked.
High concentration of radiotherapy in conjunction with chemoradiation therapy promotes and expedites damage of tissue cells and vasculature. HBOT raises oxygen levels in hypoxic tissue, stimulates angiogenesis and fibroplasias, and is an effective and powerful treatment for postoperative wounds in oral, pharyngeal, and laryngeal carcinoma surgeries. In contrast, HBOT has also been proven to help those suffering with hyposalivation, a salivary gland hypofunction. Studies show that patients with hyposalivation may also face complications in regard to active respiratory infection. There were 60.4% of the 274 studied facing challenges associated with acute respiratory infection and hyposalivation while 35.5% of the 274 patients only suffered from hyposalivation. The human mouth serves as the only direct entranceway into the respiratory apparatus, thus leading to the digestive tract.
HBOT is considered an effective treatment amongst those suffering as it has the potential to reduce medical and dental treatment costs and limit the negative effects of radiation amongst those suffering, thus improving the patient’s quality of life.
Mandibular osteomyelitis is a rare, non-suppurative, chronic inflammatory disease of an unknown genesis that is associated with the bone marrow, cortical bone, periosteum, as well as blood vessels and nerves. It is an unresponsive infection that results from dormant bacteria. It is commonly distinguished as an area with minimal pus formation, fistula, or bony sequestrate formation. After HBOT admission, patients have reported lack of both pain and swelling. The average patient has received 40 treatments. HBOT works by favoring the action of the inflammatory cells and increases the host response to the targeted pain and swelling. A study conducted in 2008 proved that HBOT has an 80% success rate with a 21-day treatment. It can be concluded that HBOT is powerful in conjunction to aggressive medical and surgical treatment.
Periodontal disease is a chronic inflammatory condition of the supporting structure of the teeth. The most common cause of periodontal disease is the accumulation of bacterial plaque. If the plaque is not removed, it hardens into calculus and tartar which eventually leads to periodontal disease. Periodontal disease disturbs the soft tissues and bone that support the teeth. In periodontitis, pathobionts, and keystone pathogens such as Porphyromonas gingivalis appear in greater proportion than in health. As a keystone pathogen, P. gingivalis impairs host immune responses and appears necessary but not sufficient to cause periodontitis. Various experiments have shown HBOT to have an abbreviated benefit on pocket reduction and bacterial elimination in patients with chronic periodontitis. HBOT works by hindering the growth of subgingival obligate anaerobes and facultative anaerobes. By doing so, it advocates the healing of the infected periodontium.
When a tooth becomes too badly damaged from trauma or decay to be properly repaired, it is often recommended to be extracted from the mouth. Dental implants have become an increasingly popular method of tooth replacement prior to extraction. The implant is surgically placed into the mandible maxilla and retained during functional loading as a result of the ability for the bone to integrate with the implant as growth progresses. Osseointegration is necessary for the implant to settle properly. For osseointegration to be successful, there must be relatively high biocompatibility between the material of the implant and the jaw bone, there must be adequate quality of bone tissue, proper surgical technique, and macro- and microstructure of the implant. If the patient does not meet all of the following standards, HBOT is an advised treatment. HBOT prepares the bone and the adjacent tissue for implant retrieval.
Biofilms are commonly characterized as complex microbial communities that grow on various surfaces in nature. The emergence of biofilms within the oral cavity commonly leads to an affluence of tissue loss and bone degradation. As a result, osseointegrated dental implants are frequently used with intention of restorative treatment of the oral cavity. These implants have the potential to provide new surfaces for the biofilm bacteria to form. The resulting infections are difficult to treat with antibiotics. HBOT is commonly known to be a safe and effective means of treatment. A study done in 2012 exclaimed that the administration of high concentrations of oxygen therapy has a direct correlation to the growth of healthier tissue and higher affinity and implant-bone integration. However, there are minimal results leading to the necessity of HBOT prior to the placement of implants, only stating its effectiveness after the placement. A 15-year study conducted by Granstrom and colleagues concluded a 13.5% implant failure rate in non-irradiated patients and 53.7% in irradiated patients and 8.1% in irradiated patients receiving HBOT.
Oral submucous fibrosis
Oral submucous fibrosis is a constant debilitating disease as a result of juxta epithelial fibrosis of the oral cavity. Although success of treatment is rare, HBOT is commonly executed. This requires the patient to inhale 100% oxygen at increased atmospheric pressure often ranging between 2.0 and 2.5 atm (1 atm = 101.325 kPa) for 60–120 seconds. HBOT works to increase oxygen tension and flow to impaired tissue. HBOT also has the ability to prevent inflammation which helps expedite the healing process.
Oromandibular reconstruction is an extensive surgery with great benefits when completed successfully. The principle motive is to improve both function and aesthetic, when necessary. Surgeons manipulate the autogenous bone grafts to provide a substantial arch to articulate with the upper jaw, restoring swallowing speech, mastication and esthetics. As procedures progress in difficulty, the probability of complications heightens. An 84-year-old woman was initially diagnosed with mucosal carcinoma of the right oral cavity. During reconstruction after segmental excision of the mandible, a titanium plate was selected based on several risk factors. After the operation, the plate became exposed at the center of the chin. After various other solutions were tested, it can be concluded that HBOT was the only auspicious solution. HBOT leads to epithelization of the wound.
| Potential Complications|| |
The most general complication faced from HBOT is barotrauma. Barotrauma is injury to your body because of barometric changes or significant adjustment in water pressure. The injury specifically targets the middle ear and sinuses because of the difference in pressure between the exterior and tympanic membrane. These symptoms include but are not limited to, ear pain, dizziness and muffled hearing. If adjustments are not made to the pressure, middle ear effusions, rupture of the tympanic membrane and sinus complications arise. Due to the intimate connection between the teeth and the sinuses, dentists often encounter physiological and pathological phenomena resulting from the drastic increase in altitude.
Ontological complications, ocular or contraindications, osteogenesis, maxillary osteomyelitis, salivary gland function, and irritated oral mucosa will be further discussed.
The human body anatomy renders an intimate relationship between the teeth and the sinus cavity. When there is pressure within the sinus cavity, there is potential for it to travel to the roots of the top of your teeth, specifically within the isolated upper teeth and back molars. Specifically, the relationship of the maxillary posterior teeth with the sinus floor and buccal cortex. It has been proven through rigorous research that distance from root apex to the sinus floor increases with increased age of the patient. On the contrary, the palatal roots of maxillary first molars exhibited the highest incidence as well as the greatest mean length (1.96 mm) of protrusion into the maxillary sinus.
In consonance with Boyle’s law, a significant modification in environmental pressure results in an inverse change in volume, thus leading to significant effect on the sinus cavity. Under systematic circumstances, the Eustachian tube within the ear must be open to eliminate the pressure difference between the internal and ambient environments. When the Eustachian tube is blocked, the sinus ostia is indirectly blocked. When the pressure change exceeds this capacity, sinus barotrauma transpires. If succumbs to carbon monoxide poisoning during HBOT, the rate of sinus abnormalities of barotrauma is 66.3%. It is important to air on the side of caution for the patients with history of sinusitis, otitis media and or upper respiratory infections as they tend to have a higher frequency of sinus barotrauma. The sinus cavities cooperate with the nasal cavities through ostia and a long duct in the sinuses. When the opening in the sinus ostium that connects the nasal cavity and the sinus is blocked, the pressure is no longer equally shared between them. As the ambient pressure is increased, it is transmitted through the sinus wall and often leads to vascular congestion and edema of the sinus mucosa. If the elastic limit of the sinus mucosa is surpassed, hemorrhage will occur.
A study done in 2015 by students at the Tokyo Medical and Dental University, Japan states the complications with HBOT within the department of otolaryngology. Otology is a branch of medicine which studies normal and pathological anatomy and physiology of the ear as well as their diseases, diagnosis and treatment. The complications assessed as a result of HBOT were otalgia, ear fullness, hearing loss and tinnitus. In conclusion, it is essential for physicians to be attentive to both middle and inner ear barotrauma as probable complications following HBOT. The interest within otology complications in this article is undeviatingly relevant to the location of the sinus to the oral cavity. The thin floor of the main sinus can be found directly above the roots of the teeth towards the rear end of the oral cavity. Damage to the sinus cavity can result in damage roots of the oral cavity as they are so closely located. Damage to the roots often require extensive dental procedures such as extractions, root canals and periodontal surgeries. The amputation of the pulp as a result of infection and decay within the enamel and dentin require extensive treatment and can be harmful to the rest of the oral cavity if not properly treated in a timely manner.
Ocular complications and contraindications
HBOT increases the concentration of reactive oxygen species in blood and tissue as a result of the increase in oxygen pressure. This is often beneficial concerning various diseases but may result in ocular complications as a result. An abundance of reactive oxygen species in tissues and or deficiencies in antioxidant activity are frequent contributions to specific ocular complications such as cataracts. Cataracts are presented as opacification of the customary crystalline lens. The high concentration of reactive oxygen species and deficiencies in antioxidant activities have the ability to contribute to keratoconus, a disorder of the eye distinguished by the dissipation and prominence of the cornea. Complications such as keratoconus are commonly aggravated by exposure to additional reactive oxygen species throughout the exploitation of HBOT. The retina is extremely prone to oxidative damage as elucidated by macular degeneration and cataract as a result of the retina’s susceptibility to oxidative stress. For instance, macular degeneration commonly comprises of oxidative stress and death of the retinal pigment epithelial cells as a result of increasing age. HBOT has the potential to exaggerate these processes resulting in various complications subsiding in the retina.
For example, under normal conditions age-related macular degeneration involves oxidative stress and death of the retinal pigment epithelial cells. HBOT may exacerbate these processes. In addition to cataract, age-related macular degeneration and keratoconus, there may be other ocular diseases for which exposure to HBOT-related oxidative stress may be significantly adverse.
Periosteal distraction osteogenesis
The restoration of bone loss and complications that emerge as a result are often convoluted and potentially improbable. As a result, a new technology in which consists of creating an artificial space between the bone surface and the periosteum to generate new bone by gradually expanding the periosteum without following through with a corticotomy. This treatment process effectively prevents the potential complications as a result of the body’s immune system but also decrease the potential of an inadequate donor. A study done in 2014 on rabbits indicated a positive relationship between periosteal distraction osteogenesis and HBOT. Mature mammals treated with HBOT for 8 weeks saw that the quality and quantity of the newly formed bone were improved.
Maxillary osteomyelitis associated with osteopetrosis
Osteopetrosis is an infrequent condition which prevents growth of bone density and leads to deficient bone remodeling. The severity of the conditions range from neonatal on-set with life-threatening complications such as bone marrow failure. The most common is characterized by fractures, short stature, compressive neuropathies, hypocalcemia and attendant tetanic seizures. Specific to maxillary, it appears as a critical increase in bone density, as a result of defection of the osteoclasts within the body.
The treatment of maxillary osteomyelitis in patients with autosomal dominant osteopetrosis type II is unfeasible with merely antibiotics such as amoxicillin and clavulanic acid. The use of HBOT has been found to be successful. HBOT is crucial for bone regeneration, as it allows for a significant inflation of angiogenesis. The development of angiogenesis signifies an increase in tissue growth. Although osteopetrosis specifically affects bone density, the increase in tissue regeneration has a positive effect on the maxillofacial region.
Salivary gland function
The development of salivary glands is carried out by branching morphogenesis. The goal of the salivary gland is to produce and effectively secrete saliva. The development requires adequate functioning and harmony among epithelial, mesenchymal, neuronal and endothelial cells. Tissue bioengineering and gene-and cell therapy are commonly the most productive way to regenerate these cells. HBOT is necessary for hydroxylation of lysine and proline residues during collagen synthesis. This expedites cross linking and maturation of collagen which allows for vigorous healing, including but not excluded to the epithelial, mesenchymal, neuronal and endothelial cells. The status of the salivary glands can be validated with the machinery best known as DW-MRI. It has the potential to check the physiological and functional changes proceeding hyperbaric oxygen therapy.
Irradiated oral mucosa microvessel density
Succeeding radiation therapy, it is common to see slight eradication of cell proliferation and microvascular tissue in the oral mucosa. At high concentrations of radiation therapy, protein cell DNA is damaged beyond repair which prevents the cells from dividing, thus it can no longer survive. In the human body, RAD51AP1 is imperative for homologous recombination as it highly cooperates with and stimulates the function of RAD51 and DMC1 recombinases. Oral mucositis potentially results in an inflammatory response, repopulation, in fractioned radiotherapy protocols preceding and paralleling the epithelial changes, macrophages and fibroblasts.
Exfoliative oral cytology is commonly used as a diagnostic and prognostic methodology for overseeing patients battling oral cancer and potential malignant disorder. When the body is inflamed, there appears to be a higher concentration of lymphocytes. A high concentration of lymphocytes typically means the body is fighting off an infection. It is also common for the epithelial cells to present an abnormal folding phenotype. After application of HBOT, the density of the blood vessels and area were increased almost immediately. D2-40 positive lymphatic vessels were significantly increased in both the number and area within the sub-epithelial. There also appeared to be normal folding within the epithelial cells. The strongest results were obtained 6 months after the treatment of HBOT.
| Pliability of Hyperbaric Oxygen Therapy|| |
HBOT can be manipulated and safely utilized under various conditions. It can overcome the complication of medically-ventilated patients and provide very efficient treatments.
Acute respiratory distress syndrome
Acute respiratory distress syndrome is commonly found to be the basis of the necessity of ventilation. Acute respiratory distress syndrome results from a highly concentrated protein edema that engenders severe hypoxemia and incapacitated carbon dioxide excretion. Sepsis, pneumonia, aspiration of gastric contents, and a wide array of major traumas are often associated with the development of this condition. The neutrophil-dependent and platelet-dependent damage to the endothelial and epithelial barriers of the lung primarily cause lung injury. This injury of the lung epithelial barrier prevents removal of alveolar edema fluid and deprives the lung of adequate quantities of surfactant which delays resolution. HBOT is a safe method for patients who require mechanical ventilation. The only potential complication is regarding sedation. Sedation must be perfect prior to the treatment; otherwise patients may face ventilator asynchrony. Patient-ventilator asynchrony is the incongruous between neural inspiratory and mechanical inspiratory time. Modifications in timing, respiratory drive, respiratory muscle pressure and respiratory system mechanics influence the interaction between the patient and the ventilator.
Irradiated maxillofacial dental implants
Dental implants are artificial tooth roots made of titanium, which have the capabilities of holding various types of artificial teeth, such as crowns, bridges and dentures. These implants are anchored in the jawbone, where the bone tissue integrates with the implant to form a stable foundation for the artificial tooth. If the bone tissue does not integrate with the titanium implant, the implant is rejected and causes further complications. Implant rejection may be caused by the long-term effects on reduced vascularization comprising the implantation site. Within every natural tooth, there is an endodontium. The endodontium is in the center of the tooth, highly vascularized and surrounded by rigid dentin walls and made up of living connective tissue and cells called odontoblasts. The pulp vascular system is established by vasculogenesis during embryonic development, sprouting angiogenesis is the predominant process during regeneration and therapeutic processes. The high vascularity constitutes the pulp as an effective way to supply nutrients and remove waste. It is also responsible for regeneration and tooth transplantation.
HBOT can improve the tissue vascularity, thus increasing the implant survival rate by enhancing osteointegration within the patients. The graph below shows the significant difference regarding the implant failure rate between those treated with and without HBOT. There is clear evidence that HBOT has a positive effect on implant osteointegration.
|Figure 1: Effect of hyperbaric oxygen therapy on implant failure rate.|
Note: Data were from Lynch and Deaton.
Click here to view
Aside from lack of vascularity with the oral cavity, implants can be rejected from inflammation caused by oral microflora thus leading to peri-implantitis. Peri-implantitis is the destructive inflammatory process affecting the soft and hard tissues surrounding dental implants. The site-specific infectious diseases causes an inflammatory response in the soft tissue and leads to severe bone loss around the titanium implant.
Non-irradiated bone grafting
Bone grafting is a surgical procedure that uses transplanted bone to repair and rebuild diseased or damaged bones. Materials for the bone graft can be artificial, natural, synthetic, or even taken from the patient’s own body. The purpose of bone grafting is to facilitate healing and promote osseointegration of the titanium implant where there is not a sufficient amount of bone present in the targeted area. HBOT works in conjunction with other treatments to heal bone grafting as it has been proven to expedite the healing process. It also has the ability to facilitate the functional recovery of patients and to reduce the postoperative complications when deactivated and washed thoroughly with saline.
| Conclusion|| |
HBOT is an effective treatment in dental medicine as it facilitates the healing process and expedites the recovery of the patient. Despite the potential complications that may arise, it has various benefits. As previously stated, HBOT often works well in conjunction with other treatments.
The authors are thankful to Drs. Todd Miller, Kelly Warren, and Peter Brink for departmental support, as well as Mrs. Wendy Isser and Ms. Grace Garey for literature retrieval at the Renaissance School of Medicine at Stony Brook University.
Study design, concept and definition: KR, SP, JG, YS, IR, GJ, NLS, SAK. All authors read and approved the final version of the paper for publication.
Conflicts of interest
The authors have no conflicts of interest to declare.
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| References|| |
Hexdall E, Brave R, Kraft K, Siewers J. Diving deep into hyperbaric oxygen therapy. Nursing
Lam G, Fontaine R, Ross FL, Chiu ES. Hyperbaric oxygen therapy: exploring the clinical evidence. Adv Skin Wound Care
Carney AY. Hyperbaric oxygen therapy: an introduction. Crit Care Nurs Q
Gerth WA. Applicability of Henry’s law to hydrogen, helium, and nitrogen solubilities in water and olive oil at 37 degrees C and pressures up to 300 atmospheres. Arch Biochem Biophys
Devaraj D, Srisakthi D. Hyperbaric oxygen therapy - can it be the new era in dentistry? J Clin Diagn Res
Edwards ML. Hyperbaric oxygen therapy. Part 1: history and principles. J Vet Emerg Crit Care (San Antonio)
Lee CH, Chen WC, Wu CI, Hsia TC. Tension pneumocephalus: a rare complication after hyperbaric oxygen therapy. Am J Emerg Med
Leopardi LN, Metcalfe MS, Forde A, Maddern GJ. Ite Boerema--surgeon and engineer with a double-Dutch legacy to medical technology. Surgery
West JB. Early history of high-altitude physiology. Ann N Y Acad Sci
Thom SR. Hyperbaric oxygen: its mechanisms and efficacy. Plast Reconstr Surg
. 2011;127 Suppl 1:131S-141S.
Xiong T, Chen H, Luo R, Mu D. Hyperbaric oxygen therapy for people with autism spectrum disorder (ASD). Cochrane Database Syst Rev
Dauwe PB, Pulikkottil BJ, Lavery L, Stuzin JM, Rohrich RJ. Does hyperbaric oxygen therapy work in facilitating acute wound healing: a systematic review. Plast Reconstr Surg
Lambade P, Dawane P, Thorat P. Oral submucous fibrosis--a treatment protocol based on clinical study of 100 patients in central India. Oral Maxillofac Surg
Shamim T. Clinical utility of hyperbaric oxygen therapy in dentistry. Med Gas Res
Leiblein M, Marzi I, Sander AL, Barker JH, Ebert F, Frank J. Necrotizing fasciitis: treatment concepts and clinical results. Eur J Trauma Emerg Surg
Marcarelli M, Trovato L, Novarese E, Riccio M, Graziano A. Rigenera protocol in the treatment of surgical wound dehiscence. Int Wound J
Tahir AR, Westhuyzen J, Dass J, et al. Hyperbaric oxygen therapy for chronic radiation-induced tissue injuries: Australasia’s largest study. Asia Pac J Clin Oncol
Hyperbaric oxygen therapy: exploring the clinical evidence. Adv Skin Wound Care
Cook TJ. Late radiation necrosis of the jaw bones. J Oral Surg (Chic)
Zehr LJ, Cooper JS. Osteoradionecrosis, Mandible. StatPearls
. Treasure Island (FL): StatPearls Publishing LLC. 2018.
Sultan A, Hanna GJ, Margalit DN, et al. The use of hyperbaric oxygen for the prevention and management of osteoradionecrosis of the jaw: a Dana-Farber/Brigham and Women’s Cancer Center multidisciplinary guideline. Oncologist
Heyboer M 3rd, Wojcik SM, Grant WD, Faruqi MS, Morgan M, Hahn SS. Professional attitudes in regard to hyperbaric oxygen therapy for dental extractions in irradiated patients: a comparison of two specialties. Undersea Hyperb Med
Heyboer M, 3rd
, Wojcik SM, McCabe JB, et al. Hyperbaric oxygen and dental extractions in irradiated patients: short- and long-term outcomes. Undersea Hyperb Med
Lambade PN, Lambade D, Goel M. Osteoradionecrosis of the mandible: a review. Oral Maxillofac Surg
Ceponis P, Keilman C, Guerry C, Freiberger JJ. Hyperbaric oxygen therapy and osteonecrosis. Oral Dis
Tonnesen MG, Feng X, Clark RA. Angiogenesis in wound healing. J Investig Dermatol Symp Proc
Lu SY, Tsai CY, Lin LH, Lu SN. Dental extraction without stopping single or dual antiplatelet therapy: results of a retrospective cohort study. Int J Oral Maxillofac Surg
Nabil S, Samman N. Incidence and prevention of osteoradionecrosis after dental extraction in irradiated patients: a systematic review. Int J Oral Maxillofac Surg. 2011;40:229-243.
Vorrasi JS, Kolokythas A. Controversies in traditional oral and maxillofacial reconstruction. Oral Maxillofac Surg Clin North Am
Valadao J, Pearl J, Verma S, Helms A, Whelan H. Hyperbaric oxygen treatment for post-radiation central nervous system injury: a retrospective case series. Undersea Hyperb Med
Malallah OS, Garcia CMA, Proctor GB, Forbes B, Royall PG. Buccal drug delivery technologies for patient-centred treatment of radiation-induced xerostomia (dry mouth). Int J Pharm
Fox NF, Xiao C, Sood AJ, et al. Hyperbaric oxygen therapy for the treatment of radiation-induced xerostomia: a systematic review. Oral Surg Oral Med Oral Pathol Oral Radiol
Dequanter D, Jacobs D, Shahla M, Paulus P, Aubert C, Lothaire P. The effect of hyperbaric oxygen therapy on treatment of wound complications after oral, pharyngeal and laryngeal salvage surgery. Undersea Hyperb Med
Iwabuchi H, Fujibayashi T, Yamane GY, Imai H, Nakao H. Relationship between hyposalivation and acute respiratory infection in dental outpatients. Gerontology
Lin LC, Yau G, Lin TF, Lin TK, Tang YY, Wang KY. The efficacy of hyperbaric oxygen therapy in improving the quality of life in patients with problem wounds. J Nurs Res
Gonzalez-Navarro B, Arranz-Obispo C, Albuquerque R, Jane-Salas E, Lopez-Lopez J. Osteomyelitis of the jaw (with pathological fracture) following extraction of an impacted wisdom tooth. A case report. J Stomatol Oral Maxillofac Surg
Agarwal A, Kumar N, Tyagi A, De N. Primary chronic osteomyelitis in the mandible: a conservative approach. BMJ Case Rep
Handschel J, Brussermann S, Depprich R, et al. Evaluation of hyperbaric oxygen therapy in treatment of patients with osteomyelitis of the mandible. Mund Kiefer Gesichtschir
Chen CY, Lin KP, Lu SH, Chen YJ, Lin CF. Adjuvant hyperbaric oxygen therapy in the treatment of hemodialysis patients with chronic osteomyelitis. Ren Fail
Ma L, Hu P, Wu ZQ, Song XZ. Clinical application of vacuum sealing drainage combined with chymotrypsin in the treatment of post-traumatic mandibular osteomyelitis. Zhonghua Kou Qiang Yi Xue Za Zhi
Laudenbach JM, Simon Z. Common dental and periodontal diseases: evaluation and management. Med Clin North Am
Johnson TM. Smoking and periodontal disease. US Army Med Dep J
Costalonga M, Herzberg MC. The oral microbiome and the immunobiology of periodontal disease and caries. Immunol Lett
Nogueira-Filho GR, Rosa BT, David-Neto JR. Effects of hyperbaric oxygen therapy on the treatment of severe cases of periodontitis. Undersea Hyperb Med
Gaviria L, Salcido JP, Guda T, Ong JL. Current trends in dental implants. J Korean Assoc Oral Maxillofac Surg
Kern JS, Kern T, Wolfart S, Heussen N. A systematic review and meta-analysis of removable and fixed implant-supported prostheses in edentulous jaws: post-loading implant loss. Clin Oral Implants Res
Compton SM, Clark D, Chan S, Kuc I, Wubie BA, Levin L. Dental implants in the elderly population: a long-term follow-up. Int J Oral Maxillofac Implants
Goiato MC, Santos DM, Danelon M, Pesqueira AA, de Carvalho Dekon SF, Fajardo RS. Hyperbaric oxygen: therapy for patients with maxillofacial implants? J Craniofac Surg
Oliveira NM, Martinez-Garcia E, Xavier J, et al. Biofilm formation as a response to ecological competition. PLoS Biol
Veerachamy S, Yarlagadda T, Manivasagam G, Yarlagadda PK. Bacterial adherence and biofilm formation on medical implants: a review. Proc Inst Mech Eng H
Shandley S, Matthews KP, Cox J, Romano D, Abplanalp A, Kalns J. Hyperbaric oxygen therapy in a mouse model of implant-associated osteomyelitis. J Orthop Res
Chouinard AF, Giasson L, Fortin M. Hyperbaric oxygen therapy for head and neck irradiated patients with special attention to oral and maxillofacial treatments. J Can Dent Assoc
Kumar MA, Radhika B, Gollamudi N, Reddy SP, Yaga US. Hyperbaric oxygen therapy-a novel treatment modality in oral submucous fibrosis: a review. J Clin Diagn Res
Kumar BP, Venkatesh V, Kumar KAJ, Yadav BY, Mohan SR. Mandibular reconstruction: overview. J Maxillofac Oral Surg
Maeda T, Yamamoto Y, Tanaka S, Hayashi T. Application of vacuum-assisted closure therapy and hyperbaric oxygen therapy for an exposed titanium plate after mandible reconstruction. J Craniofac Surg
Lynch JH, Deaton TG. Barotrauma with extreme pressures in sport: from scuba to skydiving. Curr Sports Med Rep
Kumar S, Kumar PS, John J, Patel R. Barotrauma: tooth under pressure. J Mich Dent Assoc
Shokri A, Lari S, Yousef F, Hashemi L. Assessment of the relationship between the maxillary sinus floor and maxillary posterior teeth roots using cone beam computed tomography. J Contemp Dent Pract
Jang JK, Kwak SW, Ha JH, Kim HC. Anatomical relationship of maxillary posterior teeth with the sinus floor and buccal cortex. J Oral Rehabil
Wang P, Zhang XM, Zhai ZH, Li PL. MRI findings of otic and sinus barotrauma in patients with carbon monoxide poisoning during hyperbaric oxygen therapy. PLoS One
Ambiru S, Furuyama N, Aono M, Otsuka H, Suzuki T, Miyazaki M. Analysis of risk factors associated with complications of hyperbaric oxygen therapy. J Crit Care
Kiran Kumar Krishanappa S, Eachempati P, Kumbargere Nagraj S, et al. Interventions for treating oro-antral communications and fistulae due to dental procedures. Cochrane Database Syst Rev
Huang GT. Dental pulp and dentin tissue engineering and regeneration: advancement and challenge. Front Biosci (Elite Ed)
McMonnies CW. Hyperbaric oxygen therapy and the possibility of ocular complications or contraindications. Clin Exp Optom. 2015;98:122-125.
Deng H, Yuan L. Molecular genetics of congenital nuclear cataract. Eur J Med Genet
Fournie P, Touboul D, Arne JL, Colin J, Malecaze F. Keratoconus. J Fr Ophtalmol
Zhao D, Wang Y, Han D. Periosteal distraction osteogenesis: an effective method for bone regeneration. Biomed Res Int
Suer BT, Ortakoglu K, Gunaydin Y, et al. Effects of the hyperbaric oxygen on de novo bone formation during periosteal distraction. J Craniofac Surg
Stark Z, Savarirayan R. Osteopetrosis. Orphanet J Rare Dis
Jayachandran S, Kumar MS. A paradoxical presentation of rickets and secondary osteomyelitis of the jaw in Type II autosomal dominant osteopetrosis: Rare case reports. Indian J Dent Res
Carvalho PHA, Moura LB, Real Gabrielli MF, Cabrini Gabrielli MA, Antonio Pereira Filho V. Maxillary osteomyelitis associated with osteopetrosis: Systematic review. J Craniomaxillofac Surg
Grassmann JP, Schneppendahl J, Hakimi AR, et al. Hyperbaric oxygen therapy improves angiogenesis and bone formation in critical sized diaphyseal defects. J Orthop Res
Patel VN, Hoffman MP. Salivary gland development: a template for regeneration. Semin Cell Dev Biol
Bhutani S, Vishwanath G. Hyperbaric oxygen and wound healing. Indian J Plast Surg
Loimu V, Seppala T, Kapanen M, et al. Diffusion-weighted magnetic resonance imaging for evaluation of salivary gland function in head and neck cancer patients treated with intensity-modulated radiotherapy. Radiother Oncol
Parplys AC, Kratz K, Speed MC, Leung SG, Schild D, Wiese C. RAD51AP1-deficiency in vertebrate cells impairs DNA replication. DNA Repair (Amst)
Gruber S, Dorr W. Tissue reactions to ionizing radiation-Oral mucosa. Mutat Res
Shashikala R, Indira AP, Manjunath GS, Rao KA, Akshatha BK. Role of micronucleus in oral exfoliative cytology. J Pharm Bioallied Sci. 2015;7:S409-413.
Svalestad J, Hellem S, Thorsen E, Johannessen AC. Effect of hyperbaric oxygen treatment on irradiated oral mucosa: microvessel density. Int J Oral Maxillofac Surg
Matthay MA, Zemans RL. The acute respiratory distress syndrome: pathogenesis and treatment. Annu Rev Pathol
Bessereau J, Aboab J, Hullin T, et al. Safety of hyperbaric oxygen therapy in mechanically ventilated patients. Int Marit Health
Sassoon CS, Foster GT. Patient-ventilator asynchrony. Curr Opin Crit Care
Kuroshima S. Dental implant treatment in patients receiving anti-resorptive agents. Clin Calcium
Rombouts C, Giraud T, Jeanneau C, About I. Pulp vascularization during tooth development, regeneration, and therapy. J Dent Res
Demarco FF, Conde MC, Cavalcanti BN, Casagrande L, Sakai VT, Nor JE. Dental pulp tissue engineering. Braz Dent J
Shah DN, Chauhan CJ, Solanki JS. Effectiveness of hyperbaric oxygen therapy in irradiated maxillofacial dental implant patients: A systematic review with meta-analysis. J Indian Prosthodont Soc
Preethanath RS, AlNahas NW, Bin Huraib SM, et al. Microbiome of dental implants and its clinical aspect. Microb Pathog
Prathapachandran J, Suresh N. Management of peri-implantitis. Dent Res J (Isfahan)
Kumar P, Vinitha B, Fathima G. Bone grafts in dentistry. J Pharm Bioallied Sci
Hollander MHJ, Boonstra O, Timmenga NM, Schortinghuis J. Hyperbaric oxygen therapy for wound dehiscence after intraoral bone grafting in the nonirradiated patient: a case series. J Oral Maxillofac Surg
Zhang Y, Li JZ, Lu XC, et al. Intramedullary nailing combined with bone grafting for benign lesions of the proximal femur. Orthop Surg
[Table 1], [Table 2]