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Running head: INTRAVENOUS GLUTATHIONE AND DISEASE STATES1Skin Lightening Treatments: A Review on the Effect of Intravenous Glutathione in the Disease States of WomenBuhle MthombeniA Senior Thesis
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01
Consult with a healthcare provider to determine if intravenous glutathione is appropriate for the specific disease being treated.
02
Gather all necessary supplies including the glutathione solution, intravenous tubing, and syringe.
03
Follow proper sterile technique to prepare the glutathione solution and fill the syringe.
04
Clean the injection site on the patient's arm with an alcohol swab.
05
Insert the needle into the vein at a 15-30 degree angle and slowly push the glutathione solution into the vein.
06
Monitor the patient for any adverse reactions during and after the administration of intravenous glutathione.
07
Properly dispose of all used supplies and document the administration of the treatment.

Who needs intravenous glutathione and disease?

01
Intravenous glutathione may be recommended for patients with conditions such as liver disease, Parkinson's disease, chronic fatigue syndrome, or as a detoxification treatment.
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Intravenous glutathione refers to the administration of glutathione, a powerful antioxidant, directly into the bloodstream to treat or manage certain diseases, such as chronic fatigue syndrome, liver disease, and certain cancers.
Healthcare providers administering intravenous glutathione therapies are typically required to document and report the procedures and any related diseases for regulatory and health monitoring purposes.
Filling out intravenous glutathione and disease documentation involves providing patient information, treatment specifics, dosage, administration details, and any observed outcomes or side effects related to the treatment.
The purpose is to monitor the use of glutathione therapy in treating diseases, evaluate efficacy, track patient outcomes, and ensure compliance with health regulations.
Information such as patient demographics, diagnosis, dosage of glutathione administered, treatment dates, and any adverse reactions must be reported.
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