Blood irradiation therapy

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Blood irradiation therapy
SpecialtyHematology

Blood irradiation therapy is an

ultraviolet irradiation of blood kills bacteria by DNA damage and also activation of the immune system. Blood irradiation therapy is highly controversial, and has fallen from mainstream use since its heyday in the 1940s and 1950s.[1]

Blood irradiation therapy can be administered in three ways: extracorporeally, transcutaneously, and intravenously. The extracorporeal (outside the body) method removes blood from the body and irradiates it in a special

monochromatic
.

It is not related to the practice of gamma irradiation of blood in transfusion medicine.

History

In 1928, Dr. Emmet Knott and a medical student named Lester Edblom received a United States patent for a "Means for Treating Blood-Stream Infection" that incorporated a rudimentary ultraviolet bulb, vacuum extraction system and a cuvette. The "Knott Hemo-Irradiator" was used from the 1930s through the 1950s on patients with multiple infectious diseases.

George P Miley at the

poliomyelitis, non-healing wounds, and asthma
.

One of the best known and most comprehensive set of studies was published in 1947 by Dr. George Miley and Dr. Jens A Christensen (from the Blood Irradiation Clinic of the Hahnemann Medical College and Hospital of Philadelphia, Pennsylvania). The authors studied 445 cases of acute pyogenic infections and 74 cases of virus and virus-like infections. Findings included the following:

penicillin-resistant
infections have responded to the treatment. Further finding included: "We have observed that toxemias due to various virus and virus-like infections subside rapidly …” Some of the more impressive results included cases involving septic infection, 57 out of 57 cases recovered. In treating peritonitis, 16 out of 18 patients recovered. With puerperal sepsis, 14 out of 14 patients recovered. With thrombophlebitis, 34 out of 34 recovered. The authors emphasized the need to follow the protocol set for by Knott. Of importance, this protocol included the use of a chamber or cuvette with a flat quartz surface. 

Henry A Barrett at the Willard Parker Hospital in New York City, in 1940 reported on 110 cases including a number of infections. Twenty-nine different conditions were described as responding including the following: infectious arthritis, septic abortion,

acne vulgaris, and secondary anemia.[7]

This procedure fell out of favor in the late 1950s, at a time when

The U.S. Food and Drug Administration (FDA) has approved one type of this treatment[8][9] for T cell lymphoma. This particular process was developed by a team at Yale, led by Richard Edelson who developed a photopheresis machine. This machine separates the white and red blood cells. The white cells are then routed into a blood chamber, where those cells are subjected to UV light from the UVA part of the spectrum. This process uses a photosensitizing agent which enhances the effectiveness of the light.[10] Observational evidence suggests that photopheresis might be effective in the treatment of graft-versus-host disease,[11] though controlled trials are needed to support this use.[12][13]

The

fraudulently sold by alternative cancer treatment clinics in Mexico.[14]

Types

Intravenous laser blood irradiation

An intravenous blood irradiation therapy in use.
Intravenous blood irradiation

Intravenous or intravascular laser blood irradiation (ILBI) involves the

better source needed] This issue is subject to skepticism.[2]

Transcutaneous laser blood irradiation

Transcutaneous therapy applies laser light on unbroken skin in areas with large numbers of blood vessels (such as the forearm). Because of the skin acting as a barrier to the blood, absorbing low level laser energy, the power of the laser is often boosted to compensate.[16] The problem can be solved by using pulsed matrix laser light sources.[3]

Extracorporeal irradiation

Extracorporeal irradiation is used only for ultraviolet blood irradiation, that involves drawing blood out through a vein and irradiating it outside of the body.[17]

Though promoted as a treatment for cancer, a 1952 review in the

Journal of the American Medical Association[4] and another review by the American Cancer Society in 1970 concluded the treatment was ineffective.[18]

See also

References