Donor blood for neonatal exchange transfusion.
نویسندگان
چکیده
منابع مشابه
Hyperbilirubinemia Following Exchange Transfusion with G-6-PD Deficient Donor Blood
Background: The incidence of glucose-6-phosphate dehydrogenase (G-6-PD) deficiency in Iran is estimated at 10-14.9%. The donor blood in blood banks is not screened routinely for this enzyme deficiency and such blood may be used for neonatal exchange transfusion.Objective: To study the effect of G-6-PD deficient blood in neonatal exchange blood transfusion.Methods: In a prospective study, serum...
متن کاملSevere neonatal hyperbilirubinemia leading to exchange transfusion
Background :Severe neonatal hyperbilirubinemia is associated with significant morbidity and mortality. This study was conducted to investigate the causes of severe hyperbilirubinemia leading to Exchange Transfusion (ET) from March 2009 to March 2011 in Bahrami children hospital, Tehran, Iran in order to establish guidelines to prevent profound jaundice & ET. Methods : 94 neonates underwent ...
متن کاملHot Blood for Transfusion
The importance of warming up the whole blood before transfusion , parti -cularly when large amounts of stored blood is used for patients in shock or under general anesthesia is discussed. Various methods of Warming blood is presntcd and the use of high frequency Electromagnetic field for this purpose and its adv1mtagcs is introduced.
متن کاملSevere neonatal hyperbilirubinemia leading to exchange transfusion
BACKGROUND Severe neonatal hyperbilirubinemia is associated with significant morbidity and mortality. This study was conducted to investigate the causes of severe hyperbilirubinemia leading to Exchange Transfusion (ET) from March 2009 to March 2011 in Bahrami children hospital, Tehran, Iran in order to establish guidelines to prevent profound jaundice & ET. METHODS 94 neonates underwent ET fo...
متن کاملNeonatal paracetamol poisoning: treatment by exchange transfusion.
The metabolism and excretion of paracetamol was studied in an infant of 29 weeks' gestation who was exposed to the drug when his mother ingested 32.5 g 16 hours before delivery. We have confirmed that sulphation is the major pathway and that the mixed function oxidase system is sufficiently active at this gestational age to produce hepatotoxic metabolic products. As most of the recognised drug ...
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ژورنال
عنوان ژورنال: BMJ
سال: 1978
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.1.6108.301-c