News & Research

Hyperbaric Oxygen Therapy has been used for the better part of two centuries. Search our  arhives below for past HBOT news and research or scroll down for the latest.

The Latest HBOT News & Research

Clinical Trial – The Effects of Height and Weight Adjusted Dose of Local Anesthetic.

At our centre a conventional dose of 12 mg of hyperbaric bupivacaine in combination with a
short acting opioid fentanyl (to increase block density) and a long acting opioid morphine
(to provide post-operative pain relief ) is used for spinal anesthesia for cesarean
section.However, larger doses of local anesthetic drug when used in caesarean section
commonly cause low blood pressure and requires drugs (vasopressors) to treat it. In our study
the investigators will standardize the doses of both opioids (fentanyl/morphine) and adjust
the dose of local anesthetic (bupivacaine) based on the patients height and weight .One of
the obvious challenges anesthesiologists face is providing adequate anesthesia to the patient
whilst minimizing harmful side effects. Our primary concern is the low blood pressure as an
effect of the spinal anesthetic as it is harmful to both mother and the baby. The
investigators propose that the extent of surgical anesthetic block, which is dependent on
height and weight in our adjusted dose group, will provide adequate anesthesia for surgery
and minimise maternal low blood pressure.

Clinical Trial – Spinal Anaesthesia and Severe Preeclampsia

The use of spinal anesthesia in pre-eclamptic pregnant woman is of considerable benefit, as
these patients present particular hazards with general anaesthesia, such as concerns for
rapid airway control and cerebral blood flow alterations during induction of general
anaesthesia and intubation However, the incidence of hypotension is high during spinal
anesthesia for Cesarean section and it may approach values up to 95 %.

Clinical Trial – Colloid Pre-Loading on D-Dimer During Cesarean Section Under Spinal Anesthesia

Maternal hypotension is the most frequent complication of a spinal Anesthesia. The prevention
of spinal hypotension appears more likely to decrease the frequency and severity of
associated adverse maternal symptoms than the treatment of established hypotension.
Intravenous fluid administration prior to spinal anesthesia for caesarean section is accepted
standard practice. The choice of fluid depends on individual and institutional habit,
material cost (crystalloid is considerably cheaper) and the perceived relative benefits and
risks. Uncommon but potentially serious adverse effect of colloids is impaired coagulation.
Although pregnancy is associated with hypercoagulability, little is known about the effects
of colloid preloading on coagulation in pregnant patients.

Clinical Trial – HBOT Global Functioning After Stroke

Stroke is one of the leading causes of disability and death in North America and Europe. Up
to 30% of stroke survivors never recuperate completely and suffer from loss of function and
poor quality of life. To improve recovery after stroke, innovative interventions should be a
priority.

Hyperbaric oxygen therapy (HBOT) is an intermittent inhalation of 100% oxygen in a hyperbaric
chamber at a pressure higher than 1 absolute atmosphere (ATA). There is a growing body of
evidence that HBOT can enhance ability of brain to changes its structure (neuroplasticity) in
order to recover. Exercise program during HBOT can augment the effect. Although, recent
randomized controlled trials in patients with chronic brain injury showed promising results,
there are no studies demonstrating combine effect HBOT and exercise rehabilitation program on
stroke recovery.

The proposed study investigates feasibility, safety and efficacy of using a combination of
HBOT and exercise program to improve arm function recovery in chronic stroke patients. In
this pilot randomized control trial, investigators will compare the combination of HBOT and
the focused rehabilitation exercise program versus exercise program alone on recovery of arm
function in patients with chronic stroke.

Clinical Trial – Hyperbaric Oxygen Therapy and Acute Kidney Injury

Kidney injury is a serious complication of cardiac surgery that occurs in up to 30% of
patients and increases the risk of adverse outcomes. Kidney injury initiates when oxygen
supply to the kidney drops below levels that are needed for normal cellular function, causing
tissue oxygen deficiency (hypoxia), activation of the inflammatory cascade, and oxidative
stress. Together, these events further impair tissue oxygenation, culminating in impaired
kidney function due to cellular injury and death.

There are no effective therapies for kidney injury after cardiac surgery, but there is
evidence that recovery is possible if the processes of injury – i.e., impaired oxygen
delivery, increased inflammatory response, and oxidative stress – are ameliorated soon after
the onset of injury. Hyperbaric oxygen therapy (HBOT) – which entails the intermittent
inhalation of 100% oxygen in a hyperbaric chamber at a pressure higher than one absolute
atmosphere (> 760 mmHg) – has been shown to positively affect all of these processes (i.e.,
to improve tissue oxygenation, reduce inflammation, and reduce oxidative stress). Thus, we
hypothesized that HBOT will reduce the severity of kidney injury after cardiac surgery if it
is initiated soon after onset of injury. This hypothesis has not been tested in humans, but
is supported by animal studies.

In this first-in-human, unblinded, controlled pilot trial, 20 adult patients who develop
severe kidney injury soon after cardiac surgery will be randomized (after obtaining informed
consent from the patient or surrogate) to standard-of-care or early HBOT. Severe kidney
injury will be defined as a ≥30% drop in kidney function within 6 hours of surgery (as
determined by change in creatinine from before surgery to Intensive Care Unit (ICU)
admission). This degree of injury occurs in ~ 2% of patients and is associated with a 12-fold
increase in the risk of complete kidney failure (requiring dialysis) or death. Patients will
be excluded if they have any relative or absolute contraindications to HBOT (e.g., severe
ventricular dysfunction, ventricular assist device, severe respiratory dysfunction,
pneumothorax, bronchospasm).