Ornithine Transcarbamylase De... Health Article

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Long-term management

The severity of the disorder is the most important factor in determining long-term treatment of OTC deficiency. The most severely affected individuals, usually infant males, should have liver transplants. As previously mentioned, the urea cycle and OTCs function occur in the liver. The transplantation immediately corrects OTC deficiency. Episodes of life-threatening ammonemia are prevented, although monitoring of tissue levels of ammonia is suggested. Another important benefit is that the transplant allows the child to develop and grow in a normal manner, without the threat of developmental delay or mental retardation. Transplants are now recommended even for children less than one year of age with a severe form of the disorder.

Two problems with liver transplants exist, however. First, it is difficult to obtain a liver from among the limited supply of donors, especially if the child is not currently hospitalized. The second problem arises from the way in which organs are assigned. Persons who are critically ill receive priority in organ donor lists. This means children whose disease is manageable may not be able to receive a transplant.

Second, children with transplants must have their immune system suppressed. The immune system fights off, and lets one recover from infections like colds, flus, and chicken pox. However, it also fights the introduction of an organ from someone else's body, even a relative—except identical twins. Thus, as long as a person has a transplant, that person must have their immune system suppressed so that the transplanted organ is not killed by the body it is in. The problem with immune suppression is that a person is much more likely to become sick. This disadvantage is far outweighed by the advantages of normal mental development and the prevention of death in patients with severe OTC deficiency.

Patients in rural areas, or areas where there is no immediate access to a hospital equipped to care for a patient with an acute attack of hyperammonemia, should also be strongly considered for a liver transplant if the patient is predisposed to attacks of life-threatening hyperammonemia.

For less severely affected children, or children unable to obtain a liver transplant, long-term therapy consists of a combination of drugs, usually oral, sodium phenylbutyrate, and diet. This bypasses the normal process of the breakdown of protein into urea in the liver, which is the usual way that ammonia leaves the body. Children with OTC deficiency are placed on a low protein diet so their protein breakdown system does not become overwhelmed and lead to hyperammonemia. Children with OTC deficiency are also given arginine, an amino acid, which, for reasons that are unclear, causes more nitrogen, which is part of ammonia, to be excreted in the urine, and lowers blood ammonia. Dietary regimens vary from patient to patient based on their age, size, and the severity of the disorder. A nutrition expert must be consulted when developing an appropriate diet. The most strict diet consists of vitamin supplements and no protein other than essential amino acids. Essential amino acids are those that cannot be made by the body and must be obtained through food. Since proteins are made up of amino acids, and only amino acids, that means this diet is extremely restrictive. It also means that very little ammonia is left in the bloodstream since most of the otherwise free ammonia is tied up in the synthesis of the non-essential amino acids, amino acids made by the body itself.

Any chronic disease is stressful for a family. Parents and patients should consider support and information groups like the National Urea Cycle Disorders Foundation.

Short-term management

Short-term management of attacks of crisis hyperammonemia (severe acute hyperammonemia) consists of dialysis and drug therapy. Dialysis and large doses of the drugs sodium benzoate and sodium phenylacetate and doses of arginine are used to decrease the levels of ammonia in the blood. These methods are used together due to their synergistic effect.

Dialysis is a process where a toxic substance is removed from the blood. This can best be understood by pouring a small amount of cola into a glass. Now pour a large amount of water into it. In this way, the cola is "watered down" or diluted. Ammonia is diluted in a similar way using dialysis. Blood is removed from a patient and run through a hose. At one point, this hose runs through a tank made up of liquid that contains all the components of blood, but no ammonia (this liquid is like the water in the water and cola example). Thus, ammonia spreads throughout the blood and the liquid surrounding the hose (the same way cola will spread out throughout water added to the glass) and the amount of ammonia in the blood is reduced. By continuously pumping blood through the hose and changing the liquid around the hose, most of the ammonia can be removed from the blood. All of the really large particles, like red blood cells, are also kept in the blood because the hose has holes that are only large enough to let smaller particles like ammonia out while keeping red blood cells in.

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Author Info: Michael V. Zuck Ph D, Thomson Gale, Gale, Detroit, Gale Encyclopedia of Genetic Disorders Part II, 2005
 
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