TY - JOUR T1 - Randomised controlled trial of prophylactic etamsylate: follow up at 2 years of age JF - Archives of Disease in Childhood - Fetal and Neonatal Edition JO - Arch Dis Child Fetal Neonatal Ed SP - F183 LP - F187 DO - 10.1136/fn.84.3.F183 VL - 84 IS - 3 AU - D Elbourne AU - S Ayers AU - H Dellagrammaticas AU - A Johnson AU - M Leloup AU - S Lenoir-Piat Y1 - 2001/05/01 UR - http://fn.bmj.com/content/84/3/F183.abstract N2 - AIM To assess the role of etamsylate* in reducing the risk of haemorrhagic brain damage and its consequences.DESIGN Follow up of babies recruited into a randomised controlled trial.METHODS A total of 334 infants born before 33 weeks gestation in France and Greece were randomly allocated within the first four hours of birth either to receive etamsylate or to act as controls. The principal outcomes in the trial were death or impairment and/or disability at the age of 2 years.RESULTS Fifty nine children were lost to follow up. A total of 115 (34%) either died or had some impairment or disability, and 88 (26%) either died or had severe impairment or disability at 2 years of age. These outcomes did not differ significantly between the two randomised groups: relative risks and 95% confidence intervals 1.14 (0.78 to 1.4) and 1.17 (0.82 to 1.68) respectively. The findings were similar for all the prespecified subgroup analyses stratified by key prognostic factors at trial entry: country of birth, gestational age < or ⩾ 29 weeks, inborn or outborn, age < or ⩾  1 hour, and with or without cerebral scan abnormality.CONCLUSION These findings do not support the use of etamsylate. Other strategies need to be evaluated for the prevention of mortality and morbidity in these vulnerable infants. Key messagesKey messagesThe findings from the only published follow up of children from a randomised controlled trial of etamsylate do not support its use when given within the first four hours of birth to infants born before 33 weeks gestationCentres in Greece and France recruited 334 infants into the trial, and did not find that etamsylate reduced the risk of haemorrhagic brain damage or its consequences in terms of death or impairment and/or disabilityOther strategies need to be evaluated for the prevention of mortality and morbidity in these vulnerable infants ER -