A Sechrist Monoplace hyperbaric chamber at the Moose Jaw Union Hospital, Saskatchewan, Canada
Hyperbaric medicine is medical treatment in which an ambient pressure greater than sea level atmospheric pressure is a necessary component. The treatment comprises hyperbaric oxygen therapy (HBOT), the medical use of oxygen at an ambient pressure higher than atmospheric pressure, and therapeutic recompression for decompression illness, intended to reduce the injurious effects of systemic gas bubbles by physically reducing their size and providing improved conditions for elimination of bubbles and excess dissolved gas.
The equipment required for hyperbaric oxygen treatment consists of a pressure chamber, which may be of rigid or flexible construction, and a means of delivering 100% oxygen. Operation is performed to a predetermined schedule by trained personnel who monitor the patient and may adjust the schedule as required. HBOT found early use in the treatment of decompression sickness, and has also shown great effectiveness in treating conditions such as gas gangrene and carbon monoxide poisoning. More recent research has examined the possibility that it may also have value for other conditions such as cerebral palsy and multiple sclerosis, but no significant evidence has been found.
Therapeutic recompression is usually also provided in a hyperbaric chamber. It is the definitive treatment for decompression sickness and may also be used to treat arterial gas embolism caused by pulmonary barotrauma of ascent. In emergencies divers may sometimes be treated by in-water recompression if a chamber is not available and suitable diving equipment to reasonably secure the airway is available.
A number of hyperbaric treatment schedules have been published over the years for both therapeutic recompression and hyperbaric oxygen therapy for other conditions.
- 1 Scope
- 2 Medical uses
- 3 Contraindications
- 4 Therapeutic principles
- 5 Hyperbaric chambers
- 6 Treatments
- 7 Costs
- 8 Research
- 9 History
- 10 See also
- 11 References
- 12 Further reading
- 13 External links
Hyperbaric medicine includes hyperbaric oxygen treatment, which is the medical use of oxygen at greater than atmospheric pressure to increase the availability of oxygen in the body; and therapeutic recompression, which involves increasing the ambient pressure on a person, usually a diver, to treat decompression sickness or an air embolism by eliminating bubbles that have formed within the body.
In the United States the Undersea and Hyperbaric Medical Society, known as UHMS, lists approvals for reimbursement for certain diagnoses in hospitals and clinics. The following indications are approved (for reimbursement) uses of hyperbaric oxygen therapy as defined by the UHMS Hyperbaric Oxygen Therapy Committee:
- Air or gas embolism;
- Carbon monoxide poisoning;
- Central retinal artery occlusion;
- Clostridal myositis and myonecrosis (gas gangrene);
- Crush injury, compartment syndrome, and other acute traumatic ischemias;
- Decompression sickness;
- Enhancement of healing in selected problem wounds;
- Exceptional blood loss (anemia);
- Idiopathic sudden sensorineural hearing loss;
- Intracranial abscess;
- Mucormycosis, especially rhinocerebral disease in the setting of diabetes mellitus;
- Necrotizing soft tissue infections (necrotizing fasciitis);
- Osteomyelitis (refractory);
- Delayed radiation injury (soft tissue and bony necrosis);
- Skin grafts and flaps (compromised);
- Thermal burns.
Evidence is insufficient as of 2013 to support its use in autism, cancer, diabetes, HIV/AIDS, Alzheimer's disease, asthma, Bell's palsy, cerebral palsy, depression, heart disease, migraines, multiple sclerosis, Parkinson's disease, spinal cord injury, sports injuries, or stroke. Despite the lack of evidence, in 2015, the number of people utilizing this therapy has continued to rise.
There is limited evidence that hyperbaric oxygen therapy improves hearing in patients with sudden sensorineural hearing loss who present within two weeks of hearing loss. There is some indication that HBOT might improve tinnitus presenting in the same time frame.
HBOT in diabetic foot ulcers increased the rate of early ulcer healing but does not appear to provide any benefit in wound healing at long term follow-up. In particular, there was no difference in major amputation rate. For venous, arterial and pressure ulcers, no evidence was apparent that HBOT provides an improvement over standard treatment.
There is some evidence that HBOT is effective for late radiation tissue injury of bone and soft tissues of the head and neck. Some people with radiation injuries of the head, neck or bowel show an improvement in quality of life. Importantly, no such effect has been found in neurological tissues. The use of HBOT may be justified to selected patients and tissues, but further research is required to establish the best people to treat and timing of any HBO therapy.
There is tentative evidence for HBOT in traumatic brain injury. As of 2012 there is insufficient evidence to support its general use in TBI. In stroke HBOT does not show benefit. HBOT in multiple sclerosis has not shown benefit and routine use is not recommended.
A 2007 review of HBOT in cerebral palsy found no difference compared to the control group. Neuropsychological tests also showed no difference between HBOT and room air and based on caregiver report, those who received room air had significantly better mobility and social functioning. Children receiving HBOT were reported to experience seizures and the need for tympanostomy tubes to equalize ear pressure, though the incidence was not clear.
The toxicology of the treatment has recently been reviewed by Ustundag et al. and its risk management is discussed by Christian R. Mortensen, in light of the fact that most hyperbaric facilities are managed by departments of anaesthesiology and some of their patients are critically ill.
The only absolute contraindication to hyperbaric oxygen therapy is untreated pneumothorax. The reason is concern that it can progress to tension pneumothorax, especially during the decompression phase of therapy, although treatment on oxygen-based tables may avoid that progression. The COPD patient with a large bleb represents a relative contraindication for similar reasons.[page needed] Also, the treatment may raise the issue of Occupational health and safety (OHS), which has been encountered by the therapist.[clarification needed]
Patients should not undergo HBO therapy if they are taking or have recently taken the following drugs:
- Doxorubicin (Adriamycin) – A chemotherapeutic drug. This drug has been shown to potentiate cytotoxicity during HBO therapy.
- Cisplatin – Also a chemotherapeutic drug.
- Disulfiram (Antabuse) – Used in the treatment of alcoholism.
- Mafenide acetate (Sulfamylon) – Suppresses bacterial infections in burn wounds
The following are relative contraindications -- meaning that special consideration must be made by specialist physicians before HBO treatments begin:
- Cardiac disease[clarification needed]
- COPD with air trapping - can lead to pneumothorax during treatment.
- Upper respiratory infections – These conditions can make it difficult for the patient to equalise their ears or sinuses, which can result in what is termed ear or sinus squeeze.
- High fevers – In most cases the fever should be lowered before HBO treatment begins. Fevers may predispose to convulsions.
- Emphysema with CO2 retention – This condition can lead to pneumothorax during HBO treatment due to rupture of an emphysematous bulla. This risk can be evaluated by x-ray.[clarification needed]
- History of thoracic (chest) surgery – This is rarely a problem and usually not considered a contraindication. However, there is concern that air may be trapped in lesions that were created by surgical scarring. These conditions need to be evaluated prior to considering HBO therapy.
- Malignant disease: Cancers thrive in blood-rich environments but may be suppressed by high oxygen levels. HBO treatment of individuals who have cancer presents a problem, since HBO both increases blood flow via angiogenesis and also raises oxygen levels. Taking an anti-angiogenic supplement may provide a solution. A study by Feldemier, et al. and recent NIH funded study on Stem Cells by Thom, et al., indicate that HBO is actually beneficial in producing stem/progenitor cells and the malignant process is not accelerated.
- Middle ear barotrauma is always a consideration in treating both children and adults in a hyperbaric environment because of the necessity to equalise pressure in the ears.
Pregnancy is not a relative contraindication to hyperbaric oxygen treatments,[page needed] although it may be for underwater diving. In cases where a pregnant woman has carbon monoxide poisoning there is evidence that lower pressure (2.0 ATA) HBOT treatments are not harmful to the fetus, and that the risk involved is outweighed by the greater risk of the untreated effects of CO on the fetus (neurologic abnormalities or death.) In pregnant patients, HBO therapy has been shown to be safe for the fetus when given at appropriate levels and “doses” (durations). In fact, pregnancy lowers the threshold for HBO treatment of carbon monoxide-exposed patients. This is due to the high affinity of fetal hemoglobin for CO.[page needed]
The therapeutic consequences of HBOT and recompression result from multiple effects. The increased overall pressure is of therapeutic value in the treatment of decompression sickness and air embolism as it provides a physical means of reducing the volume of inert gas bubbles within the body; Exposure to this increased pressure is maintained for a period long enough to ensure that most of the bubble gas is dissolved back into the tissues, removed by perfusion and eliminated in the lungs. The improved concentration gradient for inert gas elimination (oxygen window) by using a high partial pressure of oxygen increases the rate of inert gas elimination in the treatment of decompression sickness. For many other conditions, the therapeutic principle of HBOT lies in its ability to drastically increase partial pressure of oxygen in the tissues of the body. The oxygen partial pressures achievable using HBOT are much higher than those achievable while breathing pure oxygen under normobaric conditions (i.e. at normal atmospheric pressure); A related effect is the increased oxygen transport capacity of the blood. Under normal atmospheric pressure, oxygen transport is limited by the oxygen binding capacity of hemoglobin in red blood cells and very little oxygen is transported by blood plasma. Because the hemoglobin of the red blood cells is almost saturated with oxygen under atmospheric pressure, this route of transport cannot be exploited any further. Oxygen transport by plasma, however is significantly increased using HBOT as the stimulus. Recent evidence suggests that exposure to hyperbaric oxygen (HBOT) mobilizes stem/progenitor cells from the bone marrow by a nitric oxide (NO) -dependent mechanism. This mechanism may account for the patient cases that indicate recovery of damaged organs and tissues with HBOT.
The traditional type of hyperbaric chamber used for therapeutic recompression and HBOT is a rigid shelled pressure vessel. Such chambers can be run at absolute pressures typically about 6 bars (87 psi), 600,000 Pa or more in special cases. Navies, professional diving organizations, hospitals, and dedicated recompression facilities typically operate these. They range in size from semi-portable, one-patient units to room-sized units that can treat eight or more patients. The larger units may be rated for lower pressures if they are not primarily intended for treatment of diving injuries.
A rigid chamber may consist of:
- a pressure vessel that is generally made of steel or aluminium with the view ports (windows) made of acrylic;
- one or more human entry hatches—small and circular or wheel-in type hatches for patients on gurneys;
- the entry lock that allows human entry—a separate chamber with two hatches, one to the outside and one to the main chamber, which can be independently pressurized to allow patients to enter or exit the main chamber while it is still pressurized.
- a low volume medical or service airlock for medicines, instruments, and food;
- transparent ports or closed-circuit television that allows technicians and medical staff outside the chamber to monitor the patient inside the chamber;
- an intercom system allowing two-way communication;
- an optional carbon dioxide scrubber—consisting of a fan that passes the gas inside the chamber through a soda lime canister;
- a control panel outside the chamber to open and close valves that control air flow to and from the chamber, and regulate oxygen to hoods or masks;
- an over-pressure relief valve.
- a built-in breathing system (BIBS) to supply and exhaust treatment gas.
- a fire suppression system.
Flexible monoplace chambers are available ranging from collapsible flexible aramid fiber-reinforced chambers which can be disassembled for transport via truck or SUV, with a maximum working pressure of 2 bar above ambient complete with BIBS allowing full oxygen treatment schedules. to portable, air inflated "soft" chambers that can operate at between 0.3 and 0.5 bars (4.4 and 7.3 psi) above atmospheric pressure with no supplemental oxygen, and longitudinal zipper closure.
Hard chambers and soft chambers are not equivalent in efficacy and safety as they are different in many aspects.
In the larger multiplace chambers, patients inside the chamber breathe from either "oxygen hoods" – flexible, transparent soft plastic hoods with a seal around the neck similar to a space suit helmet – or tightly fitting oxygen masks, which supply pure oxygen and may be designed to directly exhaust the exhaled gas from the chamber. During treatment patients breathe 100% oxygen most of the time to maximise the effectiveness of their treatment, but have periodic "air breaks" during which they breathe chamber air (21% oxygen) to reduce the risk of oxygen toxicity. The exhaled treatment gas must be removed from the chamber to prevent the buildup of oxygen, which could present a fire risk. Attendants may also breathe oxygen some of the time to reduce their risk of decompression sickness when they leave the chamber. The pressure inside the chamber is increased by opening valves allowing high-pressure air to enter from storage cylinders, which are filled by an air compressor. Chamber air oxygen content is kept between 19% and 23% to control fire risk (US Navy maximum 25%). If the chamber does not have a scrubber sysytem to remove carbon dioxide from the chamber gas, the chamber must be isobarically ventilated to keep the CO2 within acceptable limits.
Smaller "monoplace" chambers can only accommodate the patient, and no medical staff can enter. The chamber may be pressurised with pure oxygen or compressed air. If pure oxygen is used, no oxygen breathing mask or helmet is needed, but the cost of using pure oxygen is much higher than that of using compressed air. If compressed air is used, then an oxygen mask or hood is needed as in a multiplace chamber. Most monoplace chambers can be fitted with a demand breathing system for air breaks. In low pressure soft chambers, treatment schedules may not require air breaks, because the risk of oxygen toxicity is low due to the lower oxygen partial pressures used (usually 1.3 ATA), and short duration of treatment.
For alert, cooperative patients, air breaks provided by mask are more effective than changing the chamber gas because they provide a quicker gas change and a more reliable gas composition both during the break and treatment periods.
Initially, HBOT was developed as a treatment for diving disorders involving bubbles of gas in the tissues, such as decompression sickness and gas embolism, It is still considered the definitive treatment for these conditions. The chamber treats decompression sickness and gas embolism by increasing pressure, reducing the size of the gas bubbles and improving the transport of blood to downstream tissues. The high concentrations of oxygen in the tissues are beneficial in keeping oxygen-starved tissues alive, and have the effect of removing the nitrogen from the bubble, making it smaller until it consists only of oxygen,[clarification needed] which is re-absorbed into the body. After elimination of bubbles, the pressure is gradually reduced back to atmospheric levels. Hyperbaric chambers are also used for animals, especially race horses where a recovery is worth a great deal to their owners. It is also used to treat dogs and cats in pre- and post-surgery treatment to strengthen their systems prior to surgery and then accelerate healing post surgery.
The slang term, at some facilities, for a cycle of pressurization inside the HBOT chamber is "a dive". An HBOT treatment for longer-term conditions is often a series of 20 to 40 dives, or compressions. These dives last for about an hour and can be administered via a hard, high-pressure chamber or a soft, low-pressure chamber—the major difference being per-dive "dose" of oxygen. Many conditions do quite well with the lower dose, lower cost-per-hour, soft chambers.
Emergency HBOT for decompression illness follows treatment schedules laid out in treatment tables. Most cases employ a recompression to 2.8 bars (41 psi) absolute, the equivalent of 18 metres (60 ft) of water, for 4.5 to 5.5 hours with the casualty breathing pure oxygen, but taking air breaks every 20 minutes to reduce oxygen toxicity. For extremely serious cases resulting from very deep dives, the treatment may require a chamber capable of a maximum pressure of 8 bars (120 psi), the equivalent of 70 metres (230 ft) of water, and the ability to supply heliox as a breathing gas.
U.S. Navy treatment charts are used in Canada and the United States to determine the duration, pressure, and breathing gas of the therapy. The most frequently used tables are Table 5 and Table 6. In the UK the Royal Navy 62 and 67 tables are used.
The Undersea and Hyperbaric Medical Society (UHMS) publishes a report that compiles the latest research findings and contains information regarding the recommended duration and pressure of the longer-term conditions.
Home and out-patient clinic treatment
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There are several sizes of portable chambers, which are used for home treatment. These are usually referred to as "mild personal hyperbaric chambers", which is a reference to the lower pressure (compared to hard chambers) of soft-sided chambers. Food and Drug Administration (FDA) approved chambers for use with room air are available in the USA and may go up to 4.4 pounds per square inch (psi) above atmospheric pressure, which equals 1.3 atmospheres absolute (ATA), equivalent to a depth of 10 feet of sea water. In the US, these "mild personal hyperbaric chambers" are categorized by the FDA as CLASS II medical devices and requires a prescription in order to purchase one or take treatments. Personal hyperbaric chambers are only FDA approved to reach 1.3 ATA. While hyperbaric chamber distributors and manufacturers cannot supply a chamber in the US with any form of elevated oxygen delivery system, a physician can write a prescription to combine the two modalities, as long as there is a prescription for both hyperbarics and oxygen. The most common option (but not approved by FDA) some patients choose is to acquire an oxygen concentrator which typically delivers 85–96% oxygen as the breathing gas. Because of the high circulation of air through the chamber, the total concentration of oxygen in the chamber never exceeds 25% as this can increase the risk of fire. Oxygen is never fed directly into soft chambers but is rather introduced via a line and mask directly to the patient. FDA approved oxygen concentrators for human consumption in confined areas used for HBOT are regularly monitored for purity (+/- 1%) and flow (10 to 15 liters per minute outflow pressure). An audible alarm will sound if the purity ever drops below 80%. Personal hyperbaric chambers use 120 volt or 220 volt outlets. Ranging in size from 21 inches up to 40 inches in diameter these chambers measure between 84 in (7 ft) to 120 in (10 ft) in length. The soft chambers are approved by the FDA for the treatment of altitude sickness, but are commonly used for other "off-label" purposes.
Possible complications and concerns
There are risks associated with HBOT, similar to some diving disorders. Pressure changes can cause a "squeeze" or barotrauma in the tissues surrounding trapped air inside the body, such as the lungs, behind the eardrum, inside paranasal sinuses, or trapped underneath dental fillings. Breathing high-pressure oxygen may cause oxygen toxicity. Temporarily blurred vision can be caused by swelling of the lens, which usually resolves in two to four weeks.
Effects of pressure
Patients inside the chamber may notice discomfort inside their ears as a pressure difference develops between their middle ear and the chamber atmosphere. This can be relieved by ear clearing using the Valsalva maneuver or other techniques. Continued increase of pressure without equalising may cause ear drums to rupture, resulting in severe pain. As the pressure in the chamber increases further, the air may become warm.
To reduce the pressure, a valve is opened to allow air out of the chamber. As the pressure falls, the patient’s ears may "squeak" as the pressure inside the ear equalizes with the chamber. The temperature in the chamber will fall. The speed of pressurization and de-pressurization can be adjusted to each patient's needs.
HBOT is recognized by Medicare in the United States as a reimbursable treatment for 14 UHMS "approved" conditions. A 1-hour HBOT session may cost between $165 and $250 in private clinics, and over $2,000 in hospitals. U.S. physicians (either M.D., D.O., D.D.S., D.M.D., D.C.) may lawfully prescribe HBOT for "off-label" conditions such as stroke, and migraine. Such patients are treated in outpatient clinics. In the United Kingdom most chambers are financed by the National Health Service, although some, such as those run by Multiple Sclerosis Therapy Centres, are non-profit. In Australia, HBOT is not covered by Medicare as a treatment for multiple sclerosis. The average U.S. hospital charge is $1,800.00 per 90 minute HBOT treatment. China and Russia treat more than 80 maladies, conditions and trauma with HBOT.
The University of Birmingham's 2012 guidance to West Midlands primary care trusts and clinical commissioning groups concluded "The primary research studies investigating the efficacy of HBO are remarkable for the consistent poor quality of the published clinical trials as well as the lack of evidence demonstrating significant health benefits. There is a lack of adequate clinical evidence to support the view that HBO therapy is efficacious for any of the indications for which it is being used".
Tentative evidence shows a possible benefit in cerebrovascular diseases. The clinical experience and results so far published has promoted the use of HBO therapy in patients with cerebrovascular injury and focal cerebrovascular injuries. However, the power of clinical research is limited because of the shortage of randomized controlled trials.
A 2010 review of studies of HBOT applied to wounds from radiation therapy reported that, while most studies suggest a beneficial effect, more experimental and clinical research is needed to validate its clinical use.
The use of air at raised ambient pressure for the treatment of illness is recorded from 1662 for afflictions of the lung, by Henshaw. It is unlikely to have had any significant effect.
Junod built a chamber in France in 1834 to treat pulmonary conditions at pressures between 2 and 4 atmospheres absolute.
During the following century “pneumatic centres” were established in Europe and the USA which used hyperbaric air to treat a variety of conditions.
Orval J Cunningham, a professor of anaesthesia at the University of Kansas in the early 1900s observed that people suffering from circulatory disorders did better at sea level than at altitude and this formed the basis for his use of hyperbaric air. In 1918 he successfully treated patients suffering from the Spanish flu with hyperbaric air. In 1930 the American Medical Association forced him to stop hyperbaric treatment, since he did not provide acceptable evidence that the treatments were effective.
The English scientist Joseph Priestley discovered oxygen in 1775. Shortly after its discovery, there were reports of toxic effects of hyperbaric oxygen on the central nervous system and lungs, which delayed therapeutic applications until 1937, when Behnke and Shaw first used it in the treatment of decompression sickness.
In 1955 and 1956 Churchill-Davidson, in the UK, used hyperbaric oxygen to enhance the radiosensitivity of tumours, while Ite Boerema, at the University of Amsterdam, successfully used it in cardiac surgery.
In 1961 WH Brummelkamp et al. published on the use of hyperbaric oxygen in the treatment of clostridial gas gangrene.
In 1962 Smith and Sharp reported successful treatment of carbon monoxide poisoning with hyperbaric oxygen.
The Undersea Medical Society (now Undersea and Hyperbaric Medical Society) formed a Committee on Hyperbaric Oxygenation which has become recognized as the authority on indications for hyperbaric oxygen treatment.
- Undersea and Hyperbaric Medical Society
- South Pacific Underwater Medicine Society
- Decompression chamber
- Hyperbaric treatment schedules
- Gesell, Laurie B. (2008). Hyperbaric Oxygen Therapy Indications. The Hyperbaric Oxygen Therapy Committee Report (12th ed.). Durham, NC: Undersea and Hyperbaric Medical Society. ISBN 0-930406-23-0.
- "Indications for hyperbaric oxygen therapy". Undersea & Hyperbaric Medical Society. 2011. Retrieved 21 August 2011.
- Undersea and Hyperbaric Medical Society. "Air or Gas Embolism". Retrieved 2011-08-21.
- Undersea and Hyperbaric Medical Society. "Carbon Monoxide". Retrieved 2011-08-21.
- Piantadosi CA (2004). "Carbon monoxide poisoning". Undersea & Hyperbaric Medicine. 31 (1): 167–77. PMID 15233173.
- Undersea and Hyperbaric Medical Society. "Cyanide Poisoning". Retrieved 2011-08-21.
- Hall AH, Rumack BH (Sep 1986). "Clinical toxicology of cyanide". Annals of Emergency Medicine. 15 (9): 1067–1074. doi:10.1016/S0196-0644(86)80131-7. PMID 3526995.
- Takano T, Miyazaki Y, Nashimoto I, Kobayashi K (Sep 1980). "Effect of hyperbaric oxygen on cyanide intoxication: in situ changes in intracellular oxidation reduction". Undersea Biomedical Research. 7 (3): 191–7. PMID 7423657.
- Undersea and Hyperbaric Medical Society. "Central Retinal Artery Occlusion". Retrieved 2014-05-30.
- Undersea and Hyperbaric Medical Society. "Clostridal Myositis and Myonecrosis (Gas gangrene)". Retrieved 2011-08-21.
- Hart GB, Strauss MB (1990). "Gas Gangrene - Clostridial Myonecrosis: A Review". J. Hyperbaric Med. 5 (2): 125–144.
- Zamboni WA, Riseman JA, Kucan JO (1990). "Management of Fournier's Gangrene and the role of Hyperbaric Oxygen". J. Hyperbaric Med. 5 (3): 177–186.
- Undersea and Hyperbaric Medical Society. "Crush Injury, Compartment syndrome, and other Acute Traumatic Ischemias". Retrieved 2011-08-21.
- Bouachour G, Cronier P, Gouello JP, Toulemonde JL, Talha A, Alquier P (Aug 1996). "Hyperbaric oxygen therapy in the management of crush injuries: a randomized double-blind placebo-controlled clinical trial". The Journal of Trauma. 41 (2): 333–9. doi:10.1097/00005373-199608000-00023. PMID 8760546.
- Undersea and Hyperbaric Medical Society. "Decompression Sickness or Illness and Arterial Gas Embolism". Retrieved 2011-08-21.
- Brubakk, A. O.; T. S. Neuman (2003). Bennett and Elliott's physiology and medicine of diving (5th Rev ed.). United States: Saunders Ltd. p. 800. ISBN 0-7020-2571-2.
- Acott, C. (1999). "A brief history of diving and decompression illness". South Pacific Underwater Medicine Society Journal. 29 (2). ISSN 0813-1988. OCLC 16986801. Retrieved 2008-03-18.
- Undersea and Hyperbaric Medical Society. "Enhancement of Healing in Selected Problem Wounds". Retrieved 2011-08-21.
- Zamboni WA, Wong HP, Stephenson LL, Pfeifer MA (Sep 1997). "Evaluation of hyperbaric oxygen for diabetic wounds: a prospective study". Undersea & Hyperbaric Medicine. 24 (3): 175–9. PMID 9308140.
- Kranke P, Bennett M, Roeckl-Wiedmann I, Debus S (2004). Kranke P, ed. "Hyperbaric oxygen therapy for chronic wounds". The Cochrane Database of Systematic Reviews (2): CD004123. doi:10.1002/14651858.CD004123.pub2. PMID 15106239.
- Abidia A, Laden G, Kuhan G, Johnson BF, Wilkinson AR, Renwick PM, Masson EA, McCollum PT (Jun 2003). "The role of hyperbaric oxygen therapy in ischaemic diabetic lower extremity ulcers: a double-blind randomised-controlled trial". European Journal of Vascular and Endovascular Surgery. 25 (6): 513–518. doi:10.1053/ejvs.2002.1911. PMID 12787692.
- Kalani M, Jörneskog G, Naderi N, Lind F, Brismar K (2002). "Hyperbaric oxygen (HBO) therapy in treatment of diabetic foot ulcers. Long-term follow-up". Journal of Diabetes and its Complications. 16 (2): 153–158. doi:10.1016/S1056-8727(01)00182-9. PMID 12039398.
- Chen, J (2003). "The Effects of Hyperbaric Oxygen Therapy on Diabetic Retinopathy". Investigative Ophthalmology & Visual Science. 44 (5): 4017–B720.
- Chang YH, Chen PL, Tai MC, Chen CH, Lu DW, Chen JT (Aug 2006). "Hyperbaric oxygen therapy ameliorates the blood-retinal barrier breakdown in diabetic retinopathy". Clinical & Experimental Ophthalmology. 34 (6): 584–589. doi:10.1111/j.1442-9071.2006.01280.x. PMID 16925707.
- Basile C, Montanaro A, Masi M, Pati G, De Maio P, Gismondi A (2002). "Hyperbaric oxygen therapy for calcific uremic arteriolopathy: a case series". Journal of Nephrology. 15 (6): 676–80. PMID 12495283.
- Undersea and Hyperbaric Medical Society. "Severe Anemia".
- Hart GB, Lennon PA, Strauss MB (1987). "Hyperbaric oxygen in exceptional acute blood-loss anemia". J. Hyperbaric Med. 2 (4): 205–210. Retrieved 2008-05-19.
- Undersea and Hyperbaric Medical Society. "Idiopathic Sudden Sensorineural Hearing Loss". Retrieved 2014-05-30.
- Undersea and Hyperbaric Medical Society. "Intracranial Abscess". Retrieved 2011-08-21.
- Lampl LA, Frey G, Dietze T, Trauschel M (1989). "Hyperbaric Oxygen in Intracranial Abscesses". J. Hyperbaric Med. 4 (3): 111–126. Retrieved 2008-05-19.
- Chamilos, G; Kontoyiannis, DP (2015). "Chapter 133: Aspergillus, Candida, and other opportunistic mold infections of the lung". In Grippi, MA; Elias, JA; Fishman, JA; Kotloff, RM; Pack, AI; Senior, RM. Fishman's Pulmonary Diseases and Disorders (5th ed.). McGraw-Hill. p. 2065. ISBN 978-0-07-179672-9.
- Undersea and Hyperbaric Medical Society. "Necrotizing Soft Tissue Infections". Retrieved 2011-08-21.
- Escobar SJ, Slade JB, Hunt TK, Cianci P (2005). "Adjuvant hyperbaric oxygen therapy (HBO2)for treatment of necrotizing fasciitis reduces mortality and amputation rate". Undersea & Hyperbaric Medicine. 32 (6): 437–43. PMID 16509286.
- Undersea and Hyperbaric Medical Society. "Refractory Osteomyelitis". Retrieved 2011-08-21.
- Mader JT, Adams KR, Sutton TE (1987). "Infectious diseases: pathophysiology and mechanisms of hyperbaric oxygen". J. Hyperbaric Med. 2 (3): 133–140. Retrieved 2008-05-16.
- Kawashima M, Tamura H, Nagayoshi I, Takao K, Yoshida K, Yamaguchi T (2004). "Hyperbaric oxygen therapy in orthopedic conditions". Undersea & Hyperbaric Medicine. 31 (1): 155–62. PMID 15233171.
- Undersea and Hyperbaric Medical Society. "Hyperbaric Oxygen Treatments for Complications of radiation Therapy". Retrieved 2011-08-21.
- Zhang LD, Kang JF, Xue HL (Jul 1990). "Distribution of lesions in the head and neck of the humerus and the femur in dysbaric osteonecrosis". Undersea Biomedical Research. 17 (4): 353–8. OCLC 2068005. PMID 2396333.
- Lafforgue P (Oct 2006). "Pathophysiology and natural history of avascular necrosis of bone". Joint, Bone, Spine : Revue du Rhumatisme. 73 (5): 500–7. doi:10.1016/j.jbspin.2006.01.025. PMID 16931094.
- Undersea and Hyperbaric Medical Society. "Skin Grafts and Flaps Compromised". Retrieved 2011-08-21.
- Undersea and Hyperbaric Medical Society. "Thermal Burns". Retrieved 2011-08-21.
- Cianci P, Lueders H, Lee H, Shapiro R, Sexton J, Williams C, Green B (1988). "Adjunctive Hyperbaric Oxygen Reduces the Need for Surgery in 40–80% Burns". J. Hyperbaric Med. 3 (2): 97–101. Retrieved 2008-05-16.
- "Hyperbaric Oxygen Therapy: Don't Be Misled". Food and Drug Administration. August 22, 2013.
- Bennett M, Heard R (2004). Bennett MH, ed. "Hyperbaric oxygen therapy for multiple sclerosis". The Cochrane Database of Systematic Reviews (1): CD003057. doi:10.1002/14651858.CD003057.pub2. PMID 14974004.
- Walker, Joseph. "Hyperbaric Oxygen Therapy Gets More Popular as Unapproved Treatment". Wall Street Journal. Retrieved 2015-03-14.
- Bennett, M. H.; Kertesz, T.; Perleth, M.; Yeung, P.; Lehm, J. P. (17 October 2012). "Hyperbaric oxygen for idiopathic sudden sensorineural hearing loss and tinnitus (Review)". Cochrane Database of Systematic Reviews. 2012 (10). doi:10.1002/14651858.CD004739.pub4. Retrieved 18 February 2016.
- Lauvrak, Vigdis; Frønsdal, Katrine Bjørnebek; Ormstad, Sari Susanna; Vaagbø, G; Fure, Brynjar (10 March 2015). Effectiveness of Hyperbaric Oxygen Therapy in patients with Late Radiation Tissue Injury or Diabetic Foot Ulcer. ISBN 978-82-8121-945-8.
- Kranke P, Bennett MH, Martyn-St James M, Schnabel A, Debus SE (Apr 2012). "Hyperbaric oxygen therapy for chronic wounds". The Cochrane Database of Systematic Reviews. 4 (4): CD004123. doi:10.1002/14651858.CD004123.pub3. PMID 22513920.
- Bennett MH, Feldmeier J, Hampson N, Smee R, Milross C (2012). "Hyperbaric oxygen therapy for late radiation tissue injury". The Cochrane Database of Systematic Reviews. 5 (5): CD005005. doi:10.1002/14651858.CD005005.pub3. PMID 22592699.
- Bennett, MH; Trytko, B; Jonker, B (12 December 2012). "Hyperbaric oxygen therapy for the adjunctive treatment of traumatic brain injury.". The Cochrane database of systematic reviews. 12: CD004609. doi:10.1002/14651858.CD004609.pub3. PMID 23235612.
- Carson S, McDonagh M, Russman B, Helfand M (Dec 2005). "Hyperbaric oxygen therapy for stroke: a systematic review of the evidence". Clinical rehabilitation. 19 (8): 819–33. doi:10.1191/0269215505cr907oa. PMID 16323381.
- Bennett, MH; Weibel, S; Wasiak, J; Schnabel, A; French, C; Kranke, P (12 November 2014). "Hyperbaric oxygen therapy for acute ischaemic stroke.". The Cochrane database of systematic reviews. 11: CD004954. doi:10.1002/14651858.CD004954.pub3. PMID 25387992.
- Bennett M, Heard R (Apr 2010). "Hyperbaric oxygen therapy for multiple sclerosis". CNS neuroscience & therapeutics. 16 (2): 115–24. doi:10.1111/j.1755-5949.2009.00129.x. PMID 20415839.
- McDonagh MS, Morgan D, Carson S, Russman BS (Dec 2007). "Systematic review of hyperbaric oxygen therapy for cerebral palsy: the state of the evidence". Developmental Medicine and Child Neurology. 49 (12): 942–7. doi:10.1111/j.1469-8749.2007.00942.x. PMID 18039243.
- Collet JP, Vanasse M, Marois P, Amar M, Goldberg J, Lambert J, Lassonde M, Hardy P, Fortin J, Tremblay SD, Montgomery D, Lacroix J, Robinson A, Majnemer A (Feb 2001). "Hyperbaric oxygen for children with cerebral palsy: a randomised multicentre trial. HBO-CP Research Group". Lancet. 357 (9256): 582–6. doi:10.1016/S0140-6736(00)04054-X. PMID 11558483.
- "Hyperbaric Oxygen Therapy". American Cancer Society. 14 April 2011. Retrieved February 2015. Check date values in:
- Ustundag A, Duydu Y, Aydin A, Eken A, Dundar K, Uzun G (Oct 2008). "Evaluation of the potential genotoxic effects of hyperbaric oxygen therapy". Toxicology Letters. 180: S142. doi:10.1016/j.toxlet.2008.06.792.
- Mortensen, Christian Risby (2008). "Hyperbaric oxygen therapy". Current Anaesthesia & Critical Care. Elsevier. 19 (5–6): 333–337. doi:10.1016/j.cacc.2008.07.007.
- Jain, K.K. "Indications, Contraindications, and Complications of HBO Therapy". (PDF). pp. 75–80 http://www.oxygenrescuecarecentersofamerica.com/pdf/information/Chp%208%20Indications%20Contraindications%20and%20Complcations%20of%20HBO%20Therapy.pdf. Retrieved 22 September 2016. Missing or empty
- Broome JR, Smith DJ (Nov 1992). "Pneumothorax as a complication of recompression therapy for cerebral arterial gas embolism". Undersea biomedical research. 19 (6): 447–55. PMID 1304671.
- Marx, JA, ed. (2002). "chapter 194". Rosen’s Emergency Medicine: Concepts and Clinical Practice (5th ed.). Mosby. ISBN 978-0323011853.
- CAMJ (2008). "Fracture of the maxillary bone during hyperbaric oxygen therapy". Retrieved 17 December 2008.
- Takenaka S, Arimura T, Higashi M, Nagayama T, Ito E (Aug 1980). "Experimental study of bleomycin therapy in combination with hyperbaric oxygenation". Nihon Gan Chiryo Gakkai shi. 15 (5): 864–75. PMID 6159432.
- Stubbs JM, Johnson EG, Thom SR (2005). "Trends Of Treating Patients, That Have Received Bleomycin Therapy In The Past, With Hyperbaric Oxygen Treatment (Hbot) And A Survey Of Considered Absolute Contraindications To Hbot". Undersea Hyperb Med abstract. 32 (supplement). Retrieved 2008-05-23.
- Feldmeier J, Carl U, Hartmann K, Sminia P (Spring 2003). "Hyperbaric oxygen: does it promote growth or recurrence of malignancy?". Undersea & Hyperbaric Medicine. 30 (1): 1–18. PMID 12841604.
- Van Hoesen KB, Camporesi EM, Moon RE, Hage ML, Piantadosi CA (Feb 1989). "Should hyperbaric oxygen be used to treat the pregnant patient for acute carbon monoxide poisoning? A case report and literature review". JAMA. 261 (7): 1039–43. doi:10.1001/jama.1989.03420070089037. PMID 2644457.
- Elkharrat D, Raphael JC, Korach JM, Jars-Guincestre MC, Chastang C, Harboun C, Gajdos P (1991). "Acute carbon monoxide intoxication and hyperbaric oxygen in pregnancy". Intensive Care Medicine. 17 (5): 289–92. doi:10.1007/BF01713940. PMID 1939875.
- U.S. Navy Supervisor of Diving (Apr 2008). "20". U.S. Navy Diving Manual (PDF). SS521-AG-PRO-010, revision 6. 5. U.S. Naval Sea Systems Command. Archived (PDF) from the original on March 31, 2014. Retrieved 2009-06-29.
- Jørgensen TB, Sørensen AM, Jansen EC (April 2008). "Iatrogenic systemic air embolism treated with hyperbaric oxygen therapy". Acta Anaesthesiologica Scandinavica. 52 (4): 566–568. doi:10.1111/j.1399-6576.2008.01598.x. PMID 18339163.
- Behnke, Albert R (1967). "The isobaric (oxygen window) principle of decompression". Trans. Third Marine Technology Society Conference, San Diego. The New Thrust Seaward. Washington DC: Marine Technology Society. Retrieved 20 July 2016.
- Van Liew, Hugh D; Conkin, J; Burkard, ME (1993). "The oxygen window and decompression bubbles: estimates and significance". Aviation, Space, and Environmental Medicine. 64 (9): 859–65. ISSN 0095-6562. PMID 8216150.
- Thom SR, Bhopale VM, Velazquez OC, Goldstein LJ, Thom LH, Buerk DG (April 2006). "Stem cell mobilization by hyperbaric oxygen". American Journal of Physiology. Heart and Circulatory Physiology. 290 (4): H1378–H1386. doi:10.1152/ajpheart.00888.2005. PMID 16299259.
- U.S. Navy Supervisor of Diving (Apr 2008). "Chapter 21: Recompression Chamber Operation". U.S. Navy Diving Manual. Volume 5: Diving Medicine and Recompression Chamber Operations (PDF). SS521-AG-PRO-010, Revision 6. U.S. Naval Sea Systems Command. Archived (PDF) from the original on March 31, 2014. Retrieved 2009-06-29.
- Malnati, Peggy (2015-04-30). "Uncompromising composite hyperbaric oxygen chamber closes the gap". compositesworld.com newsletter. Composites World. Retrieved 29 March 2016.
- Staff (2014). "Hematocare : The revolution at 3 ata". Gaumond Medical Group Inc. Retrieved 29 March 2016.
- Staff. "Hyperlite folding portable hyperbaric chambers" (PDF). Technical specifications. London: SOS Ltd. Retrieved 29 March 2016.
- www.oxyhealth.com. "Portable Hyperbaric Chambers | Hyperbaric Oxygen Chamber | Hyperbaric Oxygen". Oxyhealth.com. Retrieved 2010-09-25.
- Wood, S (2005). "Air break masks for monoplace chambers". Undersea and Hyperbaric Medical Society, Inc. Retrieved 8 April 2016.
- Raleigh, G.W. (1988). "Air Breaks in the Sechrist Model 2500-B Monoplace Hyperbaric Chamber.". Journal of Hyperbaric Medicine. Undersea and Hyperbaric Medical Society, Inc. Retrieved 8 April 2016.
- "Undersea and Hyperbaric Medical Society". Uhms.org. Retrieved 2011-08-21.
- "Product Classification, Chamber, Hyperbaric". United States Food and Drug Administration. Retrieved 2011-08-22.
- Fitzpatrick DT, Franck BA, Mason KT, Shannon SG (1999). "Risk factors for symptomatic otic and sinus barotrauma in a multiplace hyperbaric chamber". Undersea & Hyperbaric Medicine. 26 (4): 243–7. PMID 10642071.
- Fiesseler FW, Silverman ME, Riggs RL, Szucs PA (2006). "Indication for hyperbaric oxygen treatment as a predictor of tympanostomy tube placement". Undersea & Hyperbaric Medicine. 33 (4): 231–5. PMID 17004409.
- Stein, L (2000). "Dental Distress. The 'Diving Dentist' Addresses the Problem of a Diving-Related Toothache" (PDF). Alert Diver (January/ February): 45–48. Retrieved 2008-05-23.
- Smerz RW (2004). "Incidence of oxygen toxicity during the treatment of dysbarism". Undersea & Hyperbaric Medicine. 31 (2): 199–202. PMID 15485081.
- Butler FK (1995). "Diving and hyperbaric ophthalmology". Survey of Ophthalmology. 39 (5): 347–366. doi:10.1016/S0039-6257(05)80091-8. PMID 7604359.
- Butler FK, White E, Twa M (1999). "Hyperoxic myopia in a closed-circuit mixed-gas scuba diver". Undersea & Hyperbaric Medicine. 26 (1): 41–5. PMID 10353183.
- Gesell LB, Adams BS, Kob DG (2000). "De Novo Cataract Development Following A Standard Course Of Hyperbaric Oxygen Therapy". Undersea Hyperb Med abstract. 27 (supplement). Retrieved 2008-06-01.
- Lehm Jan P, Bennett Michael H (2003). "Predictors of middle ear barotrauma associated with hyperbaric oxygen therapy". South Pacific Underwater Medicine Society Journal. 33: 127–133. Retrieved 2009-07-15.
- Bennett MH, Wasiak J, Schnabel A, Kranke P, French C (2005). Bennett MH, ed. "Hyperbaric oxygen therapy for acute ischaemic stroke". The Cochrane Database of Systematic Reviews (3): CD004954. doi:10.1002/14651858.CD004954.pub2. PMID 16034959.
- Jain KK (1989). "Effect of Hyperbaric Oxygenation on Spasticity in Stroke Patients". J. Hyperbaric Med. 4 (2): 55–61. Retrieved 2008-08-06.
- Singhal AB, Lo EH (Feb 2008). "Advances in emerging nondrug therapies for acute stroke 2007". Stroke: A Journal of Cerebral Circulation. 39 (2): 289–291. doi:10.1161/STROKEAHA.107.511485. PMID 18187678.
- Bennett MH, French C, Schnabel A, Wasiak J, Kranke P (2008). Bennett MH, ed. "Normobaric and hyperbaric oxygen therapy for migraine and cluster headache". The Cochrane Database of Systematic Reviews (3): CD005219. doi:10.1002/14651858.CD005219.pub2. PMID 18646121.
- Eftedal OS, Lydersen S, Helde G, White L, Brubakk AO, Stovner LJ (Aug 2004). "A randomized, double blind study of the prophylactic effect of hyperbaric oxygen therapy on migraine". Cephalalgia: An International Journal of Headache. 24 (8): 639–644. doi:10.1111/j.1468-2982.2004.00724.x. PMID 15265052.
- Fife WP, Fife CE (1989). "Treatment of Migraine with Hyperbaric Oxygen". J. Hyperbaric Med. 4 (1): 7–15. Retrieved 2008-08-06.
- IN-DEEP. "Hyperbaric Oxygen Therapy for MS". Making Sense of MS Research. Retrieved 8 November 2012.
- Textbook of Hyperbaric Medicine KK Jane, 5th Edition, 2010
- "Hyperbaric oxygen therapy Guidance to commissioners" (PDF). University of Birmingham. March 2012. Retrieved 8 June 2016.
- Yoshida T, Kawashima A, Ujike T, Uemura M, Nishimura K, Miyoshi S (July 2008). "Hyperbaric oxygen therapy for radiation-induced hemorrhagic cystitis". International Journal of Urology. 15 (7): 639–641. doi:10.1111/j.1442-2042.2008.02053.x. PMID 18643783.
- Noyer CM, Brandt LJ (February 1999). "Hyperbaric oxygen therapy for perineal Crohn's disease". The American Journal of Gastroenterology. 94 (2): 318–321. doi:10.1111/j.1572-0241.1999.00848.x. PMID 10022622.
- Fischer BR, Palkovic S, Holling M, Wölfer J, Wassmann H (Jan 2010). "Rationale of hyperbaric oxygenation in cerebral vascular insult". Current Vascular Pharmacology. 8 (1): 35–43. doi:10.2174/157016110790226598. PMID 19485935.
- Michalski D, Härtig W, Schneider D, Hobohm C (Feb 2011). "Use of normobaric and hyperbaric oxygen in acute focal cerebral ischemia - a preclinical and clinical review". Acta Neurologica Scandinavica. 123 (2): 85–97. doi:10.1111/j.1600-0404.2010.01363.x. PMID 20456243.
- Spiegelberg L, Djasim UM, van Neck HW, Wolvius EB, van der Wal KG (Aug 2010). "Hyperbaric oxygen therapy in the management of radiation-induced injury in the head and neck region: a review of the literature". Journal of Oral and Maxillofacial Surgery. 68 (8): 1732–1739. doi:10.1016/j.joms.2010.02.040. PMID 20493616.
- "Aerotherapeutics". Encyclopædia Britannica. 1 (11th ed.). 1911. p. 271.
- Sharkey, Sarah (April 2000). "Current indications for hyperbaric oxygen therapy". ADF Health. Joint Health Command, Australian Department of Defence. 1 (2). Retrieved 18 December 2013.
- Brummelkamp WH, Hogendijk L, Boerema I. Treatment of anaerobic infections (clostridial myositis) by drenching the tissues with oxygen under high atmospheric pressure. Surgery, 1961; 49:299-302
- Kindwall, Eric P; Whelan, Harry T (2008). Hyperbaric Medicine Practice (3rd ed.). Flagstaff, AZ: Best Publishing Company. ISBN 978-1-930536-49-4.
- Mathieu, Daniel (2006). Handbook on Hyperbaric Medicine. Berlin: Springer. ISBN 1-4020-4376-7.
- Neubauer, Richard A; Walker, Morton (1998). Hyperbaric Oxygen Therapy. Garden City Park, NY: Avery Publishing Group. ISBN 978-0-89529-759-4.
- Jain, KK; Baydin, SA (2004). Textbook of hyperbaric medicine (4th ed.). Hogrefe & Huber. ISBN 0-88937-277-2. (6th edition from Springer in press 2016)
- Harch, Paul G; McCullough, Virginia (2010). The Oxygen Revolution. Long Island City, NY: Hatherleigh Press. ISBN 1-57826-326-3.