2016, Number 3
<< Back Next >>
Arch Inv Mat Inf 2016; 8 (3)
Risk factors of brain injury in preterm infants
Monroy RAE, García RJF, Valdés LA
Language: Spanish
References: 19
Page: 89-95
PDF size: 102.51 Kb.
ABSTRACT
Introduction: The lesion in the white matter is considered as a brain injury. It encompasses intraventricular hemorrhage, periventricular hemorrhagic infarction, periventricular leukomalacia and posthemorrhagic ventriculomegaly. It is one of the most frequent complications in the preterm newborn, increasing its incidence inversely in relation to gestational age and birth weight.
Objective: To know the risk factors of brain injury in patients from the Hospital for the Child’s Neonatal Service at the Maternal and Child Institute of the State of Mexico during the period January 2012 to December 2014.
Methodology: Retrospective, observational, transverse, descriptive, and explanatory study. Prenatal risk factors (maturation pattern, preeclampsia, maternal infection, use of indomethacin), neonatal (Apgar, birth weight, birth route, gestational age, surfactant use), laboratories (platelets, coagulation times, central glucose (respiratory distress syndrome, barotrauma, persistent ductus arteriosus, pulmonary hypertension of the newborn, sepsis and necrotizing enterocolitis) and treatment (FiO
2 for 10 days, administration of oxygen, administration of amines and ovulation), were analyzed.
Results: 25 cases were collected in this study, resulting in a prevalence of 2.2% in the presentation of encephalic lesion in three years covered by the study; of which 52% (n = 13) were intraventricular hemorrhage and 48% (n = 12) leucomalacia. With respect to the risk factors that were most associated for this neurological pathology was prematurity in 60% (n = 15); however, with no relation to weight for gestational age, since 72% (n = 18) was within the 50th percentile for their age; within the prenatal factors, the presence of maternal infections was more associated with 52% (n = 13); and in relation to the treatment the correlation with the administration of supplemental oxygen in phase II and III in 64%.
Conclusions: Preterm infants are at higher risk for brain injury, including intraventricular hemorrhage in greater numbers; they still observed other risk factors associated with such neurological pathology.
REFERENCES
Cabañas F, Pellicer A. Lesión cerebral en el niño prematuro, Protocolos Diagnóstico Terapéuticos de la AEP, Neonatología, 2008. Capítulo 27, pp. 253-269. Disponible en: https://www.aeped.es/sites/default/files/documentos/27.pdf
Cervantes-Ruiz MA, Rivera-Rueda MA, Yescas-Buendía G, Villegas-Silva R, Hernández-Peláez G. Hemorragia intraventricular en recién nacidos de pretérmino en una unidad de tercer nivel en la ciudad de México, Perinatol Reprod Hum, 2012; 26 (1): 17-24.
Paneth N. Classifying brain damage in preterm infants, J Pediatr, 1999; 134 (5): 527-529.
Gilles FH, Leviton A, Golden JA, Paneth N, Rudelli RD. Groups of histopathologic abnormalities in brains of very low birthweight infants, J Neuropathol Exp Neurol, 1998; 57 (11): 1026-1034.
Marín-Padilla M. Developmental neuropathology and impact of perinatal brain damage. II: white matter lesions on the neocortex, J Neuropathol Exp Neurol, 1997; 56 (3): 219-235.
Ballabh P. Intraventricular hemorrhage in premature infants: mechanism of disease, Pediatr Res, 2010; 67 (1): 1-8.
Ballabh P, Braun A, Nedergaard M. Anatomic analysis of blood vessels in germinal matrix, cerebral cortex, and white matter in developing infants, Pediatr Res, 2004; 56 (1): 117-124.
Ballabh P, Braun A, Nedergaard M. The blood-brain barrier: an overview: structure, regulation, and clinical implications, Neurobiol Dis, 2004; 16 (1): 1–13.
Volpe JJ, Intracranial hemorrhage: Germinal matrix hemorrhage, In: Volpe JJ, editor. Neurology of the newborn. Philadelphia: Saunders Elsevier; 2008. p. 517-288.
Sarnat HB. Role of human fetal ependyma, Pediatr Neurol, 1992; 8 (3): 163-178.
Perlman JM, McMenamin JB, Volpe JJ. Fluctuating cerebral blood-flow velocity in respiratory-distress syndrome. Relation to the development of intraventricular hemorrhage, N Engl J Med, 1983; 309 (4): 204-209.
Rennie JM, South M, Morley CJ. Cerebral blood flow velocity variability in infants receiving assisted ventilation, Arch Dis Child, 1987; 62 (12): 1247-1451.
Van Bel F, Van de Bor M, Stijnen T, Baan J, Ruys JH. Aetiological rôle of cerebral blood-flow alterations in development and extension of peri-intraventricular haemorrhage, Dev Med Child Neurol, 1987; 29 (5): 601-614.
Hellstrom M, Gerhardt H, Kalen M, Li X, Eriksson U, Wolburg H et al. Lack of pericytes leads to endothelial hyperplasia and abnormal vascular morphogenesis, J Cell Biol, 2001; 153 (3): 543-553.
Wilkinson M, Hume R, Strange R, Bell JE. Glial and neuronal differentiation in the human fetal brain 9-23 weeks of gestation, Neuropathol Appl Neurobiol, 1990; 16 (3): 193-204.
Xu H, Hu F, Sado Y, Ninomiya Y, Borza DB, Ungvari Z et al. Maturational changes in laminin, fibronectin, collagen IV, and perlecan in germinal matrix, cortex, and white matter and effect of betamethasone, J Neurosci Res, 2008; 86 (7): 1482-1500.
Mullaart RA, Hopman JC, Rotteveel JJ, Daniëls O, Stoelinga GB, De Haan AF. Cerebral blood flow fluctuation in neonatal respiratory distress and periventricular haemorrhage, Early Hum Dev, 1994; 37 (3): 179-185.
Tsuji M, Saul JP, du Plessis A, Eichenwald E, Sobh J, Crocker R et al. Cerebral intravascular oxygenation correlates with mean arterial pressure in critically ill premature infants, Pediatrics, 2000; 106 (4): 625-632.
Volpe JJ. Intraventricular hemorrhage and brain injury in the premature infant. Diagnosis, prognosis, and prevention, Clin Perinatol, 1989; 16 (2): 387-411.