Sayed Mahdi Marashi1, Hojatollah Raji2, Zeynab Nasri-Nasrabadi2, Mohammad Majidi1. 1. Trauma Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. 2. Department of Pediatrics, Children's Medical Center, Pediatric Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
To the Editor,Paraquat poisoning is a highly lethal toxicity despite advances in critical care and efforts in extracorporeal elimination [1]. After ingestion, paraquat is rapidly absorbed via the gastrointestinal tract and reaches peak plasma concentrations within the 1st hour. In many cases, by the time patients receive medical support; gastrointestinal decontamination is no longer possible.Afterward, paraquat is actively absorbed by most vital organs, and plasma concentration rapidly drops within about 4 hours [23]. This duration must be considered the optimal period to use extracorporeal elimination techniques. Fortunately, charcoal hemo- perfusion, and to a lesser extent hemodialysis, can help eliminate paraquat [2]. However, our experience indicates that most patients do not receive extracorporeal elimination during this period. Although charcoal hemoperfusion is the preferred method [2], it is not readily available, even in many tertiary care centers. To use this technique, a rapid patient transportation system is required. In contrast, hemodialysis can be used more readily in some secondary care settings, so it is a good choice in the golden period. However, some problems can be encountered. Although central venous access is easily attained, the unknown hepatitis viral marker status of a patient is a common barrier to emergency hemodialysis or charcoal hemoperfusion. It is necessary to prevent contamination of hemodialysis equipment by infectedpatients [4]. Because of the high mortality rate of paraquattoxicity and the necessity of removing considerable amounts of it from the bloodstream during the first hours, we propose that hemodialysis equipment be reserved for patients who are positive for hepatitis B surface antigen and also be used for these patients. Although there is a risk of nosocomial transmission of hepatitis B, this risk is not very high [5]. In addition, hepatitis B immunoglobulin can be used for protection immediately after the procedure if laboratory data indicate that the patient is not seropositive [6].
Authors: D Kleinknecht; A M Courouce; S Delons; C Naret; J P Adhemar; C Ciancioni; J Fermanian Journal: Clin Nephrol Date: 1977-09 Impact factor: 0.975
Authors: Rachel A Burdick; Jennifer L Bragg-Gresham; John D Woods; Sara A Hedderwick; Kiyoshi Kurokawa; Christian Combe; Akira Saito; John LaBrecque; Friedrich K Port; Eric W Young Journal: Kidney Int Date: 2003-06 Impact factor: 10.612