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No evidence of clotting of blood.
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No complications due to blood clots: (1) No destruction of the blood-deprived
tissue beyond the clot (an infarction); (2) No dislodging of a clot
that traveled within a blood vessel (an embolus) to form an infarction
in a distant organ; nor (3) many emboli forming infarctions in many
body organs that was often lethal (named Disseminated Intravascular
Coagulopathy).
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Pain in burns was relieved within minutes when heparin was dripped
or sprayed onto burn surfaces (topically).
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Pain in blisters was relieved within a minute when blister fluid was
drained and the blister were rinsed with heparin.
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Deep in body pain was relieved promptly as heparin was administered
by vein, or more slowly relieved by heparin injection into fat below
normal skin.
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Recurrent lesser pain was relieved again with a lesser amount of heparin.
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With pain relieved, no pain medicine was needed. No morphine, dilaudid,
demerol, or codeine narcotics. Therefore,
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Narcotic
complications were avoided: No distorted senses; No suppressed breathing
or heart function; No decreased intestinal activity; and No addiction.
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In addition to relief of pain, other signs of burn cellular-destruction
(inflammation) were controlled: the redness was blanched; the heat
was cooled, and the burn and body swelling was much reduced. Once
relieved they did not return with continued use of heparin.
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Swelling in body compartments was less and usually not sufficient
to compress blood vessels and stop blood flow within compartments
resulting in gangrene requiring amputation; or in loss of nerve function
producing a muscle paralysis. Thus Compartment Syndrome was largely
eliminated.
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Fewer incisions opening skin and deeper tissue to release compartment
pressure (fasciotomies) were performed.
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Inflammation itself was controlled and stopped: burns did not increase
in size as previously observed without heparin. A study of 3rd degree
experiemental burns showed that with heparin use the burns consistently
decreased in size and depth to an average 71% of original size at
9-11 days. In contrast, without use of heparin, the burns increased
in size and depth for 9-11 days, to an average 121% of original size.
This initial 50% advantage with heparin persisted into final healing.
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Burn blisters were not removed (debrided). Blisters did not become
infected as a rule. The blisters functioned as natural skin grafts
under which smooth new skin was evident when the thin dried blisters
fell (flaked) off.
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At 24 hours, heparin-treated burns were smaller in size by measurement,
drier, had less or no pain or swelling, and in some burns an early
return of blood to blood deprived and deficient tissues was evident
(revascularization).
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Saliba described production of new blood vessels and a return of blood
to blood deficient tissue, called neoangiogenesis, before neoangiogenesis
was a known effect and property of heparin. Neoangiogenesis is the
migration of the single cells that forms the wall of the smallest
blood-vessels (capillary endothelial cells) into a blood-deficient
body area (ischemic tissue), and multiplication of the endothelial
cells which then connect-up to form new capillaries which carry blood
and restore blood-flow into the ischemic areas, enabling healing for
which blood circulation is vital. In 1973 in JAMA, Journal of American
Medical Association, Saliba stated: “Unexpectedly, small blood
vessels appeared in some thick avascular white eschar. Red comma-sized
and comma-shaped structures, randomly arranged at first, increased
in length, number, and proximity; joined in a rudimentary vascular
vessel pattern; and increased in complexity, number, and proximity
until the entire area was densely revascularized erythematous structure
that by subsequent granulation and re-epithelialization evolved into
healthy healed skin without slough, debridement, skin graft, infection,
contracture, or scar.” A blood vessel tumor (hemangioma) in
one healed burn area seemed to indicate too much heparin had been
used topically. It was nearly 10 years later, early in the 1980’s,
that studies proved that heparin was the body’s neoangiogenic
biochemical.
-
Saliba
administered oral penicillin or erythromycin antibiotic to all burned
patients, who had fewer infections then previous patients not treated
with heparin. Increased delivery of antibiotic to burns by the heparin-enhanced
blood flow to the burns was one mechanism. Another reason for reduced
infections was found 2 decades later - a study showed heparin preserved
intestinal structure and reduced translocation (passage) of intestinal
bacteria into the body (sepsis) in experimental 3rd degree burns compared
to controls without heparin.
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With heparin use, fluids needed to maintain vital blood circulation
was half.
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Saliba described the enhanced amount of highly vascular granulation
tissue, whose main ingredient is collagen, without stating the mechanism
of heparin-collagen effect, because mechanisms were unknown.
-
Nearly 15 years later, Drs. KM Ramakrishnan and colleagues in Madras
(now named Chennai) India, experimented and found the mechanisms by
which heparin stimulated and regulated the production and deposition
of collagen in granulation tissue in two phases in burned patients.
<link to Ramakrishnan>
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Saliba describe enhanced healing with consistently smooth skin without
scars and contractures with heparin use topically into healing. As
with neoangiogenesis and enhanced granulation tissue, no mechanism(s)
for the heparin production of smooth skin without scars or contractures
were stated because mechanisms were not then known. Two decades later,
studies found heparin stimulated the production of primitive cells
(fibroblasts) to form increased numbers of smooth muscle cells so
no contractures resulted. The muscle cells then adequately filled
the space below the new skin, so no shortening (contracture) of the
skin surface resulted which limited movement. Similarly heparin stimulated
increased production of primitive fibroblast cells to form new dermal
cells, and aligned their inner structural rods (intracytoplasmic fibrils)
in a parallel regular pattern which resulted in smooth skin. In scars
the intracytoplasmic fibrils were in a chaotic pattern or in clumps
beneath the dermal cell membrane.
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The studies were presented in National and International Burn Meetings.
-
-
The Heparin Protocol was presented to and beneficially used by doctors
in treating over 30,500 burned patients in 18 countries (by 2007).
-
Advocated use of heparin in thermal disasters as a first response
cost-effective treatment of the many burn victims.
-
Developed a Heparin Therapy in Thermal Disasters Protocol available
free to download from the Internet Website: http://salibaburnsinstitute.org
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Organized a Global Heparin Therapy in Thermal Disaster Response System
of Doctors experienced in Heparin Therapy in many countries (In each
doctor’s link.). These doctors are willing to travel within
and adjacent to their countries to sites of thermal disasters and
within 2-24 hours consult-assist the local doctors when appropriate
in the cost-effective treatment using heparin of the many burned persons.
(View Thermal Disasters in Mexico and India link.)
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Saliba additionally researched heparin treatment of difficult-to-treat
and chronic-non-healing-wounds, ulcers, and skin problems. The evidence
is in the U.S. Patents he filled but did not use commercially. Heparin
provides cost-effective therapy for these dreaded, costly, disabling,
and often terminal ills.
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Established the Saliba Burns Institute, a global association of
burn-treating doctors dedicated to broadly informing the public
and instructing doctors, nurses, and ancillary therapists worldwide
in the safe, cost-effective addition of heparin in treatment of
burns, wounds, and difficult to treat skin problems.
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Sponsored National and International Heparin Effects in Burns Meetings,
Conferences, and Symposiums with Workshops. In the future, the meetings
will be expanded beyond burns to include wounds and skin problems.
See also: A Summary of How Heparin Improves Burns for
Patients and Doctors.