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High density oxygen (aka HBOT) not only acts as a potent bactericide, it also becomes a potent antifungal. Combined with the appropriate pharmaceuticals toxic mold and fungus are rapidly eradicated from the body using multiple physiological mechanisms. We present a dramatic intervention that saved the life of this little person
Miraculous recovery of
six-year-old Carson C’
Carson was diagnosed with lymphoblastic leukemia and, while in the hospital,
developed a severe opportunistic infection with
dissementated mucormycosis during the induction phase of his
chemotherapy. This usually fatal infection is not uncommon in the severely
immunosuppressed patients such as Carson. The infection is so rapid and lethal,
the conventional medical response is an urgent mixture of surgery (debride until
bleeding tissue is found) and antifungal agents.
In a ten-day period, Carson surgeon's removed one kidney
from Carson, his spleen and most of his colon.
Plans were made to remove the little boy's left lung and his stomach.
Staff at Children’ Hospital of San Diego did not believe that Carson would
survive the surgery and at the urging of Carson’s mother, herself an M.D. they
considered adding hypberbaric oxygen therapy (“HBOT”) for his survival. They
consulted local San Diego hospital-based HBOT centers and were unable to treat
Carson . . . “Yes, this soft-tissue infection is covered by our guidelines.
We would love to help but our wound care patients have us jammed for weeks . . .”
Children’s Hospital oncologist called our free standing HBOT Center. “Yes”
was our answer. “although HBOT has been used all around the World to eradicated
disseminated fungi such as mucormycosis for many years, using HBOT for mucormycosis is unusual
in the U.S., . . . And yes, we have
the skills to treat your patient, send him over” was the answer. And, “This
is not the first time we have treated one of your little patients from Childrens'
" (see the “Orthopedics” page
for that story -- Amci's
limb salvage, click
here)
Children’s Hospital Oncologists and Surgeons immediately called for an in-house
investigational review board (“IRB”) which reviewed the available literature.
The IRB authorized outpatient treatment for Carson with full emergency-care
ambulance transport to our Center. The little patient’s medical insurer
PacificCare reviewed the physician's orders and approved treatments.

\\\
Result: the mucor disappeared and Carson did not need additional desperate surgery. On a daily basis, Carson continues to regain weight and strength. Carson lives and will continue to do so. The Children’s Hospital primary oncologist for Carson wrote “he has had a miraculous recovery with hyperbaric oxygen contributing to this response. This infection is usually fatal, yet Carson has survived and at present remains on chemotherapy.”
Dr. Tom Millington, World-renown HBOT specialist commented:
"mucormycosis is on the list of approved conditions under the heading of
certain anaerobic infections (actinomycosis, mucormycosis). Although mucormycosis is a condition which is
approved for treatment, most facilities have never seen a case, and may be
either uncomfortable treating a patient with this, or unaware that it can be
treated."
Summary:
∙ HBOT is an adjunctive and supportive medical procedure
for patients that are dramatically ill.
∙ This soft tissue necrotizing infection is one of
the Undersea and Hyperbaric Society's (UHMS) "approved list" for hospital
treatment. Nonetheless, since this is such an unusual and dramatic situation, the
specialist physicians at Children’s Hospital
are to be congratulated for their excellent medical opinion and their courage in
stepping outside the “conventional” medical guidelines for this infection.
Medical information from Children's Hospital *



Hospital Conclusions


* Extracts taken from "Successful Treatment of Zygomycosis with the Combination of Liposmal Amphotericin B, Micafungin and GM-CSF in Two Immunocompromised Children with Lymphoid Malignancies" J willert, M Hilfiker, a Pong, J Leake, TJ Walsh Rady Childrens Hospital San Diego, Sand Diego University of California, San Diego, NCI Bethesda, MD.
Notes from the Hyperbaric O2 Center
Patient Carson C’
Six-year-old patient (Carson) was transported to San Diego Hyperbaric Center by
Ambulance for his first HBOT treatment on 11/28/06. HBOT was ordered by
specialist physicians as an adjunctive treatment modality for a fulminating
mucor infection.
The Hyperbaric Chambers: An FDA Cleared chamber to accommodate a
care-giver and the patient. The chamber is energized with 100% oxygen. No masks
or hoods were used.
Based on the 1985 pioneering work of Professor Des Gorman, Head of the School of
Medicine, Auckland New Zealand, in treating rhinocerebral mucormycosis plus the
animal studies of Van Metre et al, a treatment pressure of 2.2 ata (18 psig) was
selected. The hypothesis and in vitro studies showed the oxidative stress on
fungus to be such that high density oxygen had a potent fungicidal effect.
(http://www.medscape.com/viewarticle/432440_4)
Round One
Tx. 1 - 6 Special considerations for Carson:
LOADING: Carson had three major abdominal openings in previous
eleven days and in considerable pain. He was weak and could not stand or crawl.
The staff of the clinic devised a loading tray and Carson was transferred from
his ambulance Gurney using a pull sheet. Carson then was transferred into the
chamber from the tray using a pull sheet.
TREATMENT DEPTH: The specialist physicians had warned the staff
that Carson had a large pleural effusion on his left side. No breath sounds
could be heard and it was estimated that less than 10% vital lung function was
available on that side. There was some contemplation that the zygomucor had
invaded the entire L/H lung and that surgical removal of that lung was actually
scheduled if he HBOT did not cause dramatic improvement.
The first sequential five days of Carson’s HBOT treatments consisted on low
pressures, creeping upwards incrementally. This was to test the affected lung to
ensure that no further damage would occur with the increasing pressure.
Particular attention was paid for the decompression phase of each treatment to
ensure that there was no gas entrapment in the lung.
Carson tolerated the treatments well and equalized his ears easily. For the
first five days, the tympanic membrane was visualized and remained normal.
Tympanostomy was not considered necessary.
After some of his early HBOT Tx, Carson was nauseous, “I am having a bad
day.” This was in contrast with his pre-HBOT Tx posture of cheerful and good
mentation. Since Carson was on parenteral nutrition, it was assumed that there
was some degree of hypoglycemia. HBOT can produce dramatic drops in blood sugar
levels in diabetic and pediatric patients.
Tx. 7 – 14 Treatment depth considerations for Carson:
Based on the hypoglycemia assumption and Carson’s post-Tx vomiting, the balance
of the first series of Tx was reduced to 2 ata (14.7 psig.)
Carson’s strength had returned and he was more robust and regained strength. A
decision was made to drain the pleural effusion and his first round of HBOT
ceased for ten days.
Round Two
Tx 15 – Tx 31 Special considerations
In view of the recent chest tap, a most conservative approach was taken to this
treatment. The testing depth of 1.2 ata (2.67 psig) was selected. This to check
visceral pleural integrity to ensure that there was no potential for a
spontaneous pneumothorax. Such an event could result in a cerebral arterial gas
embolism (CAGE.) Carson tolerated the Tx well and on the following day, his
previous treatment depth of 2 ata (14.7 psig) was reintroduced.
Tx 32 - 33
With impending corrective surgery looming, Carson was treated at 2.2 Ata (18
psig.) The purpose of the increase was to blunt neutrophil mediated reperfusion
injury without rendering the host functionally neutropenic and open to
opportunistic infections. (Bartlet et al. See addendum)
Round Three
Tx 34
Five days after successful surgery, Carson commenced his third round of HBOT at
2.2 ata. (18 psig) The rational of this treatment pressure is that it
accelerates wound healing, with large shifts in collagen production, fibroblasts
and macrophage activity.
GO Carson -- Superkid !
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