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Hyperbaric Oxygen Therapy

Chronic Injuries

Hyperbaric Oxygen Therapy for Chronic Wounds

The burden that chronic wounds place on the healthcare system and its workers is substantial. It’s anticipated that 1-2% of the industrialized world’s populace will get a leg wound at some point in their lives that will require medical attention.


In 2001, it was projected that the annual cost of treating leg ulcers in the United States was $3 billion. This sum does not even account for the 2 million lost workdays. In this blog, we discuss hyperbaric oxygen therapy for chronic wounds and the benefits the hyperbaric chamber can bring.


By definition, chronic wounds are those that either don’t heal in a timely manner or don’t heal in a manner that restores anatomic and functional integrity after going through the stages of the repair process. A chronic wound can also be defined in terms of how long it takes to heal. A wound that shows no signs of improvement after eight weeks of regular treatment.


Non-healing wounds can be treated by adhering to these three basic principles: addressing the underlying issue, identifying and removing any obstacles, and creating a supportive setting for recovery. Cleansing and debridement, advanced wound dressing, and cutting-edge wound healing treatments like negative pressure wound therapy, topical growth factors, cultured skin, and macrophages are all part of the local wound treatment process.


The rate at which wounds heal is inversely proportional to how well-oxygenated those tissues are. Ischemia, or lack of blood flow to an injury, is one of the most prevalent reasons for a wound not to heal.


Hypoxia occurs when there is a lack of oxygen in a bodily region. Ischemia occurs when there is a lack of blood flow (and hence oxygen) to a portion of the body. Doctors may recommend hyperbaric oxygen therapy for chronic wounds to hasten recovery from conditions such carbon monoxide poisoning, gangrene, non-healing wounds, and infections in which tissues are oxygen-deprived.


A hyperbaric chamber is used to increase the local concentration of oxygen, which serves as the medication. The patient is exposed to higher atmospheric pressure than at sea level while breathing oxygen during therapy. This page provides background on the development of HBOT, as well as its physiological basis, clinical indications and contraindications, patient selection, treatment procedures, and adverse effects.

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Hyperbaric Oxygen Therapy for Chronic Wounds & Injuries

There is much evidence on the benefits of hyperbaric oxygen therapy for chronic wounds. Healing chronic wounds and sustaining aerobic cellular metabolism both require oxygen.


Normal metabolic activity and wound healing are severely hampered by ischemia/tissue hypoxia (oxygen levels below 30 mmHg), as anaerobic metabolism alone cannot supply enough energy for the hypoxic wound to heal.


Hyperbaric oxygen therapy consists of two parts: increased inspired oxygen concentration and increased ambient pressure.


It can be shown that the concentration of gas at the liquid’s surface and the pressure acting on the entire system are directly proportional to the amount of gas dissolved in a liquid.


With hyperbaric oxygen therapy, a patient breathes pure oxygen in a pressure room to raise his or her blood oxygen levels. Hyperoxia describes these conditions.


Patients are laid out inside a transparent chamber inflated to higher than sea level pressure and filled with 100% oxygen.


In most cases, once acclimated, the pressure is neither unpleasant nor apparent. The amount of oxygen in the blood can be increased by over 30 percent.


The increased oxygen levels carried by the blood aid the body’s immune system in fighting off infection and trigger the production of healing growth factors.


Ischemic tissues can only receive oxygen if the regional vascular supply is either unharmed or only partially damaged.


Hemoglobin’s oxygen-carrying capability plus the blood’s dissolved oxygen level is the blood’s total oxygen content.


Most of the oxygen in the blood is attached to hemoglobin and carried by the red blood cells; about 2% is free in the plasma.


Hyperbaric oxygen therapy’s efficacy in healing hypoxic and ischemic wounds is well documented.


Multiple randomized controlled clinical trials have shown that hyperbaric oxygen therapy (HBOT) is an effective supplemental treatment for diabetic ischemic foot ulcers and has dramatically decreased the rate of leg amputations.


Diabetic patients with foot ulcers who had Hyperbaric oxygen therapy had a much lower risk of undergoing a major amputation, and their wounds may have healed better after a year.


In addition, the cost-effectiveness of supplementary Hyperbaric oxygen therapy for diabetic foot ulcers was determined when compared to the cost of conventional therapy.


Breathing 100% oxygen under pressure is the basis of hyperbaric oxygen therapy.


Hyperbaric oxygen therapy is a proven method of treating decompression sickness, a possible consequence of scuba diving.


Hyperbaric oxygen therapy is also used to treat serious infections, arterial air bubbles, and diabetic or radiation-injured wounds that won’t heal.


The ambient air pressure in a chamber used for hyperbaric oxygen therapy is increased to be three times higher than that of the surrounding environment.


In these conditions, your lungs will be able to take in a large amount more oxygen than they would be able to if you were to breathe pure oxygen while the air pressure in the room was normal.


This process causes an increase in oxygen levels throughout the body, which helps the body fight infection and boosts the creation of healing growth factors and stem cells.

Related Research & Studies

Other References

Goyal A, Chonis T, Cooper JS. Hyperbaric cardiovascular effects. [Updated 2019 Jul 12]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2019 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK482231/

https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0065522

M A, Ummer VS, Maiya AG, et al. Low level laser therapy for the patients with painful diabetic peripheral neuropathy – A systematic review, Diabetes & Metabolic Syndrome: Clinical Research & Reviews, 10.1016/j.dsx.2019.07.035, (2019).

Wang EB, Kaur R, Fierro M, et al. Safety and penetration of light into the brain. Photobiomodulation in the Brain, 10.1016/B978-0-12-815305-5.00005-1, (49-66), (2019).

Mitochondrial oxidative phosphorylation defect in the heart of subjects with coronary artery disease. Ait-Aissa K, Blaszak SC, Beutner G, et al. Sci Rep. 2019 May 20; 9(1):7623. Epub 2019 May 20.

Jang S, Lewis TS, Powers C, et al. Elucidating mitochondrial electron transport chain supercomplexes in the heart during ischemia-reperfusion. Antioxid Redox Signal. 2017 Jul 1; 27(1):57-69. Epub 2016 Nov 11

Pahwa R, Jialal I. Chronic inflammation. [Updated 2019 Jun 4]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2019 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK493173/

Alberts B, Johnson A, Lewis J, et al. Molecular biology of the cell. 4th edition. New York: Garland Science; 2002. Electron-Transport Chains and Their Proton Pumps. Available from: https://www.ncbi.nlm.nih.gov/books/NBK26904/

Sharma S, Kelly TK, Jones PA. Epigenetics in cancer. Carcinogenesis. 2010;31(1):27–36. doi:10.1093/carcin/bgp220

Gauldie J. Inflammation and the aging process: devil or angel. Nutr Rev. 2007 Dec; 65(12 Pt 2):S167-9.

Hillary RF, Stevenson AJ, Cox SR, et al. An epigenetic predictor of death captures multi-modal measures of brain health. Mol Psychiatry. 2019 Dec 3; Epub 2019 Dec 3.

Banszerus VL, Vetter VM, Salewsky B, et al. Exploring the relationship of relative telomere length and the epigenetic clock in the lipid cardio cohort. Int J Mol Sci. 2019 Jun 21; 20(12). Epub 2019 Jun 21.

Sullivan J, Mirbahai L, Lord JM. Major trauma and acceleration of the ageing process. Ageing Res Rev. 2018 Dec; 48:32-39. Epub 2018 Oct 11.

Mendelsohn AR, Larrick JW. Epigenetic Drift Is a Determinant of Mammalian Lifespan. Rejuvenation Res. 2017 Oct; 20(5):430-436.

Harch, PG. Hyperbaric oxygen in chronic traumatic brain injury: oxygen, pressure, and gene therapy. Med Gas Res 5, 9 (2015) doi:10.1186/s13618-015-0030-6

General Health

Fife CE, Eckert KA, Carter MJ. An update on the appropriate role for hyperbaric oxygen: indications and evidence. Plast Reconstr Surg. 2016;138(3 Suppl):107S–16S. doi:10.1097/PRS.0000000000002714

Thom SR. Oxidative stress is fundamental to hyperbaric oxygen therapy. J Appl Physiol (1985). 2009;106(3):988–995. doi:10.1152/japplphysiol.91004.2008

Fujita N, Ono M, Tomioka T, et al. Effects of hyperbaric oxygen at 1.25 atmospheres absolute with normal air on macrophage number and infiltration during rat skeletal muscle regeneration. PLoS One. 2014;9(12):e115685. Published 2014 Dec 22. doi:10.1371/journal.pone.0115685

Vadas D, Kalichman L, Hadanny A, et al. Hyperbaric oxygen environment can enhance brain activity and multitasking performance. Front Integr Neurosci. 2017;11:25. Published 2017 Sep 27. doi:10.3389/fnint.2017.00025

Hink J, Jansen E. Are superoxide and/or hydrogen peroxide responsible for some of the beneficial effects of hyperbaric oxygen therapy? Med. Hypotheses, 57 (6) (2001), pp. 764-769.

HBOT Mechanism

Bhutani S, Vishwanath G. Hyperbaric oxygen and wound healing. Indian J Plast Surg. 2012;45(2):316–324. doi:10.4103/0970-0358.101309

Thom SR. Hyperbaric oxygen: its mechanisms and efficacy. Plast Reconstr Surg. 2011;127 Suppl 1(Suppl 1):131S–141S. doi:10.1097/PRS.0b013e3181fbe2bf

Thom SR. Oxidative stress is fundamental to hyperbaric oxygen therapy. J Appl Physiol (1985). 2009;106(3):988–995. doi:10.1152/japplphysiol.91004.2008

Wingelaar TT, Brinkman P, van Ooij PJAM, et al. Markers of Pulmonary Oxygen Toxicity in Hyperbaric Oxygen Therapy Using Exhaled Breath Analysis. Front Physiol. 2019;10:475. Published 2019 Apr 24. doi:10.3389/fphys.2019.00475

A.L. Gill, C.N.A. Bell, Hyperbaric oxygen: its uses, mechanisms of action and outcomes, QJM: An International Journal of Medicine, Volume 97, Issue 7, July 2004, Pages 385–395, https://doi.org/10.1093/qjmed/hch074

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