Hyperbaric Medicine II
Non-Diving Illness
Effects of HBOT
Types
Therapeutic
Toxic
Mechanisms
Mechanical
HBOT reduces bubble size in the bloodstream.
Follows Boyle’s Law
volume is inversely proportional to the absolute pressure
Gas Gangrene
gas bubbles in tissue tissue distention decreased perfusion
HBOT will reduce bubbles & tissue pressure increased perfusion with decreased ischemia & pain
Relevant for Air Embolisms
The therapeutic effect is achieved through mechanical reduction in bubble size.
At 5 atm a bubble is reduced to 20% of its original volume and 60% of its original diameter
pressure is crucial to therapeutic effect
Increases Oxygen Solubility in Plasma
HBOT raises oxygen tensions 10 to 13x their normal level when the patient is breathing 2.8 atm oxygen
when 6 volumes percent (6 ml per 100 ml of plasma) of oxygen are dissolved in the plasma, it is capable of carrying enough oxygen to meet the needs of the body’s tissues without RBC’s
CO2 Retention in Tissue
While breathing hyperbaric oxygen, Hb remains fully saturated within the venous circulation, blocking CO2 transport by Hb to the lungs for expulsion
Rarely causes any problem
CO2 is 50 X more soluble in the plasma than oxygen
CO2 dissolved and transported in the plasma to the lungs independent of Hb
Also CO2 is buffered by bicarbonate
slight pH shift to the acid side
interstitial lung disease are seen as hypoxemia not hypercarbia - co2 easily diffuses out.
Increased Partial Pressure of O2
Clinical use of HBOT is generally limited to a maximal partial pressure of 3 atm oxygen
Exceeding 3 atm oxygen gives no advantage and increases the toxic effects
Oxygen behaves like any other drug: too little is not enough and too much will cause harm
Effects
Reduces Blood Flow in Hyperoxic Tissues (shunt is preferentially towards the diseased segment – vasoconstriction here (the normal side which has become hyperoxic under these conditions0)
HBO causes vasoconstriction
reduces blood flow to tissues
increases peripheral vascular resistance
reduces edema
No damage to tissues from hypoxia
elevated PaO2 ( increased O2 dissolved in plasma) more than compensates for the reduction in blood flow
No Reduction (increase) of Blood Flow in Hypoxic Tissues
Vasoconstriction does not occur in hypoxic tissue i.e. chronic skin ulcers
these tissues may receive proportionately more oxygen during HBO than without HBO
plasma is able to carry dissolved oxygen to areas where red blood cells cannot go
may also beneit hypoxic tissues
Increased Healing of Hypoxic Wounds
HBOT increases tissue oxygen tension
optimizes fibroblast proliferation and
optimizes white blood cell killing capacity
stimulates angiogenesis
Ex: Skin Wound Dehiscence Following Achilles Tendon Repair
Skin Wound Following HBOT20 Tx; 2.0 atm, 90 min.
Inhibits Clostridium perfringens (a true anaerobe)
about CP A
associated diseases
Gas Gangrene
Necrotizing Fasciitis
symptoms
shock
renal failure
ards
multi organ failure
treatment
Effects of HBOT on Clostridium Perfrigens
Inhibits alpha toxin production
Detoxifies alpha toxin
within 2 hours of elaboration 
halts tissue destruction process
Increases tissue oxygen
reverses hypoxic environment
HBOT (90min of 100% O2 at 3ATM) is not the primary therapy in Gas Gangrene and Necrotizing Fascitis.It should be used in conjunction with timely surgical debridement (first) and appropriate antibiotic therapy.
The adjunctive use of HBOT therapy usually decreases the extent of radical surgical procedures
Reduces Carbon Monoxide (CO) Toxicity (prevents CO from binding; doesn’t wash it out though)
About CO
Colorless odorless gas
Byproduct of combustion
coal, wood, oil, natural gas, cigarette smoking
Competes with O2 for hemoglobin (Hb) binding sites carboxyHb (HbCO)
CO has 240X greater affinity for Hb than O2 (if you remove 20% of the O2 molcs from Hb, that is life threatening.).
Effects of HBOT on CO Toxicity
HBOT produces rapid dissociation of CO from hemoglobin
In addition Oxygen breathing at 3 atm provides immediate delivery of dissolved oxygen (6cc) into the plasma in an adequate amount to support basic tissue metabolism even while CO is significantly bound to hemoglobin
Improved Healing in Bone Repair
Effects of HBOT on Osteomyelitis
Increases oxygen tension in tissue which enhances leukocyte killing of intracellular bacteria
HBO promotes angiogenesis
increases leukocyte killing ability
Improves aminoglycoside transport across bacterial cell walls (antibiotic synergy)
Enhances osteoblastic and osteoclastic activity
Increases osteoclast activity in removing necrotic bone.
Induces fibroblast proliferation and collagen synthesis
When used according to guidelines, HBO2 is clinically efficacious and cost effective.
Improved Tissue Salvage in Crush Injury
Effects of HBOT on Crush Injuries
Increases oxygen tension leading to greater capillary oxygen diffusion.
Produces a vasoconstriction that reduces edema formation
Enhances leukocyte killing of intracellular bacteria
Diminishes the risk of infection
Improved Tissue Salvage in Burns
Effects of HBOT on Burns
Decreases edema
Decreases extravasation of fluid from wounds therefore decreasing fluid requirements during the first few days after thermal injury
Preservation of epidermal basement membranes
Hopefully Diminishing the number of surgical procedures required.
reduces the length of hospital stay and therefore cost
Effects on Blood Cells?
Multiple hyperbaric therapies may decrease the hematocrit by suppressing erythropoietin.
Reduce EPO reduced HB production.
Decreases platelet aggregation
enhances the killing ability of white blood cells 
by increasing oxygen tension (recall increase of superoxide)
Enhances Antimicrobial Activity (aminoglycosides)
Effects of HBOT on Antimicrobial Activity
Hyperoxia enhances phagocytosis and white cell oxidative killing of bacteria
enhances the activity of aminoglycocide antibiotics (only antibiotic proven to improve effectiveness with HBOT).
Decrease in Lipid Peroxidation
May improve Nerve Cell Regeneration
Suppresses Autoimmune Responses
Decreases Surfactant Production (100% O2 decreases surfactant)
Indications
Air or Gas Embolism
Decompression Sickness
CO poisoning or smoke inhalation
CO Complicated by Cyanide Poisoning in Smoke Inhalation
Crush Injury, Compartment Syndrome, and Other Traumatic Ischemias
Clostridial Myonecrosis (Gas gangrene)
Necrotizing Soft Tissue Infections, e.g. necrotizing fasciitis, myonecrosis
Enhancement of Healing in Selected Problem Wounds, e.g. diabetic ulcers
Refractory Osteomyelitis
Osteoradionecrosis
Compromised Skin Grafts and Flaps
Thermal Burns
Intracranial Abscess (anaerobes in there; most effective of treatments –i.e. the best indication).
exceptional blood loss anemia?
Contraindications
Absolute
Untreated pneumothorax
Effects of HBOT on Untreated Pneumothorax
Treatment after HBOT
Concomitant administration of doxorubicin or cis-platinum as chemotherapeutic agents for cancer
Effects of HBOT with Chemotherapeutic Agents
Disulfiram (Antabuse)
Bleomycin
Effects of HBOT + Bleomycin
Premature infants
Relative
History of Spontaneous Pneumothorax
Previous Thoracic Surgery
Severe Emphysema with CO2 Intoxication
Upper Respiratory Infection
History of Middle Ear Surgery
Seizure Disorders
Uncontrolled High Fever
Viral Respiratory Infections
Complications and Side EFfects
Barotrauma of the Ear
Round Window Blowout
Implosive Theory
Explosive Theory
Sinus Squeeze
O2 Seizures
Pulmonary Oxygen Toxicity
Finger Numbness
Serous Otitis
Lens Refractive Changes
Dental problems
Claustrophobia