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HYPERBARIC MEDICINE
Hyperbaric Chamber
It is a medical device used to
supply oxygen (O2) at greater
pressure than normal
atmospheric pressure, defined as
1 ATM.
HYPERBARIC OXYGEN THERAPY
Hermetic Cabin: It is pressurized in a stable manner (Treatment Pressure), where the patient remains during the session.
Compressors Cabinet: It enters filtered air into the cabin to reach the treatment pressure by venting in a safe manner.
Oxygen external source:It may be by hub or tank, it supplies high-concentration of O2 to the patient.
COMPONENTS
Increasing the concentration of O2 that
we inhale
Increasing the pressure of the air (environment)
O2 100% HYPERBARIA
blood oxygen (dissolved) reaching tissues little irrigated and producing other
physiological effects
HYPERBARIC OXYGEN TREATMENT (HBOT)
DALTON’s LAW
The pressure of a gas
mixture equals the sum of
the partial pressures of each
of its component gases.
HENRY’s LAW
The gases being dissolved
in liquid when they are
subjected to pressure.
OXYGEN PHYSIOLOGYPhysico-chemical Basis
OXYGEN PHYSIOLOGY
Air at sea level: Normobaria
Partial concentration of O2 : 21%
Atmospheric Pressure : 760 mmHg (1 ATA)
Pp O2 : 0,21 x 760 mmHg = 160 mmHg
Hyperbaria: 1.4 ATA
Partial concentration of O2 : 21%
Pp O2 : 0,21 x (1.4 x760 mmHg ) = 223 mmHg
OXYGEN PHYSIOLOGY
FiO2: (Inspired fraction of O2 - VN: 0,21) VH20: 47 mmHg (inner humidity– Water)PACO2: 40 mmHg (alveolar pressure CO2)CR= 0.8 (respiratory coefficient between CO2 and O2)
alveolar pressure of O2PAO2= (760 – 47) x 0.21 – 40/CR = 100 mmHgPAO2= (760 – 47) x 1 – 40/CR = 663 mmHgPAO2=(760*1.4 - 47) x 1 - 40/CR = 919 mmHg
INCREASING THE PRESSURE IN THE ALVEOLI,
DIFFUSION TO THE PLASMA INCREASES
O2 blood content
Hyperbaric effect on oxygen dissolved:
1. Normobaric air (21% O2 1 ATA 97% Hb): 0.3ml/dl dissolved oxygen2. Hyperbaric oxygen (100% 1.4 ATA 100%Hb): 2.4ml/dl dissolved oxygen
HYPEROXIA: Increases 8 fold dissolved oxygen amount (independently on Hb) O2 immediately and fully available for cell intake
HYPERBARIC OXYGEN TREATMENTEssential effect of Hyperbaric Medicine Human tissues oxigenation
Capillary density varies considerably among tissues (in average ~ 600/mm3 ) 2500-3000/mm3 in the brain, kidneys, liver, and myocardium; 300-400/mm3 in skeletal muscle < 100/mm3 in the bones, fat, connective tissue
Average separation between adjacent capillaries is ~ 40 µm microns
Most cells in living tissues are ~ 1-3 cells from a capillary.
Source: Robert A. Freitas Jr., Nanomedicine, Volume I: Basic Capabilities, Landes Bioscience, Georgetown, TX, 1999
O2 DIFFUSION: Krogh’s Model
PO2 gradients in vessels explain radial (a) and
longitudinal (b) variations of PO2. Allows to
calculate PO2 at different distances from
capillar center or arterial end: PO2 drops to
cylinder perimeter and to venous end.
ARTERIAL END
VENOUS END
a.radial
L
L
O2 DIFFUSION: Krogh’s Model
O2 tisular penetration:
pressure into hyperbaric chamber=1.4ATA generates arterial PO2=918mmHg minimal effective PO2 (tissues) = 20mmHg * penetration radius ~75µm (Distance at which PO2 = 0mmHg: 96µm)
The O2 diffusion distance rises with risingsource PO2
Under100% O2 at 1.4ATA, the O2 penetrationinto all cells and tissues is guaranteed
* *
918mmHg
PHYSIOLOGICAL EFFECTS
the gradient for O2 pressure between the alveolus and the
pulmonary capillary
Oxygen diffussion and availability in the tissues
Blood pressure of O2 and the amount of O2 dissolved (independent fromhemoglobin)
AEROBIC METABOLISM
The O2 is an essential element for cell energy production, though cellular
(mitochondrial) respiration.
Through HBOT the O2 is supplied as active ingredient, looking for maximize the tissular
oxygenation and to meet the cellular and metabolic functions.
O2
Enegry production
ATP
FREE RADICALS
Free radicals or reative oxygen species (ROS) are atoms or groups of atoms that have an unpaired electron (e-) in its outer shell. They are highly reactive
Free radicals are physiologically used by our body for multiple functions:
Immune response: against viruses and/or bacteria
Cell proliferation and mitosis
Apoptosis
ROS OXIDATIVE STRESSANTIOXIDANT
DEFENSE
OXIDIZING - ANTIOXIDANT SYSTEM BALANCE
DISBALANCE: ILLNESS
(H₂O₂ -0₂ -OH NO NOO-)
HBOT MECANISM OF ACTIONS
HYPEROXIA
ROS Production
antioxidant system enhancement
Goal: assure the O2 delivery to cells and tissues in order to
meet biochemical, metabolic and physiologic functions
HYPERBARIC OXYGEN
GENERATES A STRONG HYPEROXIA
TRIGGERS PHYSIOLOGICAL BENEFITS
VASOCONSTRICTION
ANGIOGENESIS
OSTEOGENESIS
CELLULAR IMMUNITY
PERIPHERAL AXONAL
REGENERATION
COLAGEN SYNTHESIS
OXIDATIVE STRESS AND IMMFLAMATORY RESPONSE
CEREBRAL BLOOD FLOW INCREASE AND
REDISTRIBUTION
STEM CELLS
INCREASED SUCCESS IN FLAPS AND GRAFTS
HYPEROXIA - PHYSIOLOGICAL EFFECTS
HYPEROXIA – PHYSIOLOGICAL EFFECTSVASOCONTRICTION: Hyperoxia causes vasoconstriction of small arteries reducing theimmflamation and edema. Peripheral vasoconstriction occurs in well-perfused tissues
ANGIOGENESIS: Hyperoxia / normoxia alternation is a significant angiogenic stimulus. Hyperoxiastimulates and promotes the formation of small vessels accelerating the healing process.
OSTEOGENESIS: Hyperoxia stimulates differentiation of bone-forming cells promotingosteogenesis and bone repair.
CELLULAR IMMUNITY STIMULATION: The poli-morpho nuclears (PMN), a kind a white cells, use free radicals as an anti-bacterial mechanism. O2 improves this mechanism.
PERIPHERAL AXONAL REGENERATION STIMULATION:
STIMULATES COLLAGEN SYNTHESIS: Hyperoxia stimulates collagen synthesis and fibroblasts proliferation, which are the cells that produce collagen, the key substance for wound healing and tissue repair process.
REGULATES OXIDATIVE STRESS AND IMMFLAMATORY RESPONSE: Hyperoxia acts on regulators and mediators of the inflammatory response and decreases oxidative stress producing anti-inflammatory effects with cell damage reduction.
STIMULATION IN STEM CELLS: Hyperoxia stimulates differentiation and release of stem cells, contributing to tissue repair process and formation of new blood vessels.
CEREBRAL BLOOD FLOW REDISTRIBUTION: A greater O2 availability in the brain contributes to reduce inflammation and led to greater O2 absorption at cellular level, improving treatment and rehabilitation for patients who have suffered from strokes, brain paralysis, autism spectrum disorders and neurological diseases.
GREATER SUCCESS OF FLAPS AND GRAFTS:
HYPEROXIA – PHYSIOLOGICAL EFFECTS
OXYGEN DOSE
The therapeutic effect of hyperoxia is determined by
the oxygen dose, in turn the dose of oxygen
depends on:
% of O2
Chamber pressure
Session time
Session frecuency
Number of total sessions
1 weekly session
3 weekly sessions
4 weekly sessions
2 weekly sessions
5 weekly sessions
HOW IS THE TREATMENT INDICATED?
Sessions.
10 sessions blocks, according to patient conditions and physician’s criteria.
Session duration.
The average time is 60 minutes. In acute patients could be performed 90 minutes, up to 2
times a day.
Frequency.
The physician must indicate: number of daily sessions, weekly frequency 1 to 6 and time
session.
HBOT: INDICATION – CLINICAL MEDICINE
Fibromyalgia
Chronic fatigue
Migraine y Headaches
Tinnitus
Elderly
Sleep apnea
Crohn’s disease
Adjuvant treatment to reduce inflammation and edema, relieve pain, improveperfusion, energy efficiency and life quality.
HBOT: INDICATION – TRAUMATOLOGY
Pre and post-surgery
Bacterial Progressive gangrene
Acute Traumatic Ischemia
Ligament and tendon injuries
Osteomyelitis
Non-unions
Spinal cord injury
Adjuvant treatment to accelerate healing and recovery, reduce inflammation and edema, relieve pain, reduce infection and amputation risk and improve life quality.
HBOT: INDICATION – SPORTS MEDICINE
Training
Injuries (tendon, ligaments and
muscle)
Recovery after exercise
Chronic and Subacute Fatigue
Syndrome
Adjuvant treatment to prepare athletes during training, improve energy efficiency, shorten recovery, prevent fatigue and improve injuries and trauma rehabilitation.
HBOT: INDICATION – NEUROLOGY
Stroke
Parkinson disease
Multiple Sclerosis
Spinal cord injury
Migraine
Autism spectrum disorder
Cerebral Palsy
Adjuvant treatment to reduce edema, redistribute blood flow and improve cerebral oxygenation, reduce stiffness, tremors and spasticity, improve cognitive function, neuroprotection and life quality.
HBOT: INDICATION – WOUNDS
Wounds
Ulcers - Diabetic foot
Venous ulcers
Post-surgical Wounds
Burns
Abscess
Sores
Flaps and grafts
Adjuvant treatment to reduce inflammation and edema, accelerate healing and recovery,
decrease infection and amputation risk, and improve life quality.
HBOT: INDICATION – RHEUMATOLOGY
Fibromyalgia
Rheumatoid arthritis
Arthrosis
Bone marrow edema
Bone necrosis
Osteomyelitis
Adjuvant treatment to accelerate recovery, relieve pain, reduce inflammation and edema, decrease infection risk and improve life quality.
HBOT: INDICATION – ONCOLOGY
Tumors
Radio-necrosis and radio-therapy
Adjuvant treatment to enhance radio and chemo-therapy sensitization, control tumoral
growth, relieve pain, prevent and recovery of radio-necrosis and improve life quality.
EVIDENCE AND PRESENTATION OF CASES
Several trials, case series and case reports highlight efficacy
of HBOT as successful treatment for different diseases.
*Shai Efrati et al, Plos One 2013
Hyperbaric Oxygen Induces Late Neuroplasticity in PostStroke Patients -Randomized, Prospective Trial*
A normal adult and healthy
brain should be fundamentally
yellow in the SPECT scanner.
Green indicates reduced blood
flow and oxygen. Blue and
violet represent a significant
reduction of blood flow in the
brain after 10 sessions at 1.3
ATA.
Heuser et al, 2000
Patient: Male,
Age: 60 years.
Pathology: Right leg – Ischemic ulcer/ rheumatoid arthritis
Number of sessions: 40
Patient: Male,
Age: 60 years.
Pathology: Right leg – Ischemic ulcer/ rheumatoid arthritis
Number of sessions: 40
Patient: Male
Age: 27 years old.
Pathology: Arterial venous fistula.
Number of sessions: 34
Patient: Male
Age: 27 years old.
Pathology: Arterial venous fistula.
Number of sessions: 34
Patient: Male.
Age: 60 years
Pathology: post- heart surgery injury
Number of sessions: 35
Patient: Male.
Age: 60 years.
Pathology: Right Leg. Necrosis, circulatory failure.
Number of sessions: 40
Patient: Male.
Age: 5 years
Pathology: Arterial venous malformation
Number of sessions: 70
Patient: Male.
Age: 70 years.
Pathology: Diabetic ulcer.
Number of sessions: 70
Patient: Female.
Age: 90 years.
Pathology: Bedsore
Number of sessions: 35
Patient: Female
Age: 60 years.
Pathology: Pyoderma gangrenosum
Number of sessions: 40
Patient: Female.
Age: 11 years.
Pathology: Trauma.
Number of sessions: 40
Patient: Woman.
Age: 70 years old.
Pathology: Lip melanoma (2015).
Number of sessions: 20
Patient: Male.
Age: 90 years old.
Pathology: Venous insufficiency
Number of sessions: 20
Patient: Male.
Age: 90 years old.
Pathology: Venous insufficiency
Number of sessions: 20
Absolute Untreated pneumothorax Lung Bula / Bulla
Relative Perforated eardrum Oncology treatment (Bleomycin, Cisplatin, Disulfiram, Doxorubicin) Pacemaker
Special Care HBOT produces slightly hypoglycemic. Nasal congestion. Claustrophobia. VAS pathology (Vascular Autonomic Signal) HBOT can cause mild hypertension. It is negative inotropic.
CONTRAINDICATIONS
HYPERBARIC TREATMENT WITH REVITALAIR 430 CHAMBERS
In daily use we verify the therapeutic efficacy of HBOT, like the cases of wounds we just
saw. To generate more evidence in this and other pathologies through clinical trials, we
first thoroughly study its effect on healthy volunteers:
Treatment at 1.4ATA does not modify the biochemical parameters of acute phase
inflammation and oxidative stress in healthy volunteers
Significant increase of antioxidant enzyme suggests the effect of hyperoxia
The fluctuations of biochemical parameters at 10 and 20 sessions are kept within
reference values: physiological response was conserved in healthy volunteers
Treatment is safe and well tolerated, with no adverse effects
TO CONCLUDE:
The strong HYPEROXIA increases oxygen volumedissolved in blood plasma. This greater O2 diffusionreaches less irrigated tissues
The hiperoxia produces a wide range ofPHYSIOLOGICAL BENEFITS to the body.
HYPERBARIC TREATMENT: Patient breathes highdoses of O2 in a hyperbaric enviroment
THANK YOU