Anadir Silva
Johns Hopkins University
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Obstetrics & Gynecology | 2006
Anadir Silva; Randi Smith; Christoph U. Lehmann; Elizabeth A. Johnson; Cynthia J. Holcroft; Ernest M. Graham
OBJECTIVE: To estimate whether neonates with cerebral white matter injury have significant elevations in nucleated red blood cell counts and to estimate their predictive ability in identifying injury. METHODS: This case–control study identified 176 infants born at 23–34 weeks of gestation between November 1994 and October 2004 at a single university hospital and with cerebral white matter injury characterized by periventricular leukomalacia (PVL) or ventriculomegaly due to white matter atrophy. A control was matched to each case using the subsequent delivery within 7 days of that gestational age without brain injury. RESULTS: The gestational age at birth was 27 weeks for both groups, but the cases had a significantly lower birth weight (mean ± standard deviation: 958 ± 306 g compared with 1,038 ± 381 g, P = .001). There was no difference in cesarean delivery (48% cases compared with 44% controls, P = .59). The cases had a significant increase in nucleated red blood cells per 100 white blood cells (WBC) (median, 5th percentile and 95th percentile: 22, 3 and 374 cases compared with 14, 1 and 312 controls; P = .02). Markers of chronic hypoxia, such as intrauterine growth restriction and oligohydramnios, and markers of acute hypoxia, such as an umbilical arterial pH less than 7.0 or base excess less than −12 mM, were both associated with significantly elevated neonatal nucleated red blood cell counts. A neonatal nucleated red blood cell count of 18 per 100 WBCs had a sensitivity of 56.9%, specificity of 57.9%, positive predictive value of 57.9%, and negative predictive value of 56.9% in predicting the development of cerebral white matter injury in this matched case–control sample. CONCLUSION: Preterm neonates with cerebral white matter injury have significant increases in nucleated red blood cell counts. Both acute and chronic hypoxia–ischemia can increase these counts, which limits their usefulness in timing injury. The predictive value of nucleated red blood cell counts at birth in identifying injury is poor. LEVEL OF EVIDENCE: II-2
Journal of Perinatal Medicine | 2008
Anadir Silva; Alice Cootauco; Abimbola Aina-Mumuney; Pamela K. Donohue; Ernest M. Graham
Abstract Aims: To determine the association of hypotonia and depression in neonates at or near term with metabolic acidemia at birth (umbilical arterial pH<7.0 and base excess <−12 mM). Methods: This case-control study identified 87 infants without chromosomal or congenital abnormalities born at a single university hospital between 7/91 and 10/04 with hypotonia at birth requiring resuscitation and admission to the neonatal intensive care unit that had a cord gas at delivery. Controls were the subsequent delivery with a cord gas matched by gestational age. Results: Cases and controls did not differ in gestational age (38.7±1.9, 38.6±1.9 weeks) or birth weight (3066±664, 3171±655 g, P=0.20). Cases were more likely to have a cord pH<7.0 [17 (20%) vs. 1 (1.1%), P=0.0001] and cord pH 7.0–7.1 [13 (14.9%) vs. 2 (2.3%), P=0.003]. Among the hypotonic infants, 31 (35.6%) also were depressed at birth with a 5-min Apgar <7. In the depressed subset of hypotonic neonates 14/31 (45%) had a pH<7.0. Of the 12 hypotonic neonates with seizures, 3 (25%) had pH<7.0. Multivariate analysis showed a significant association between neonatal hypotonia and hypoglycemia, umbilical arterial pH, and nucleated red blood cell count. Conclusions: Although metabolic acidemia is significantly associated with hypotonia at the time of birth, the majority of neonates with hypotonia and depression or seizures do not have objective evidence of asphyxia as measured by a cord gas at the time of delivery.
International Journal of Gynecology & Obstetrics | 2009
Hindi Stohl; Anadir Silva; Cynthia Argani; Jean Anderson
[1] Dupuis C, Charaf LA, Breviere GM, Abou P. “Infantile” form of the scimitar syndrome with pulmonary hypertension. Am J Cardiol 1993;71(15):1326–30. [2] Gudjonsson U, Brown JW. Scimitar syndrome. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu 2006:56–62. [3] Wang CC, Wu ET, Chen SJ, Lu F, Huang SC, Wang JK, et al. Scimitar syndrome: incidence, treatment, and prognosis. Eur J Pediatr 2007;167(2):155–60. [4] MiyakeM, Katayama S, Masaki K, Kubo H, Hirakawa S, Saji T. Scimitar syndrome and pregnancy: A case report. The Japanese Teratology Society Abstract Book, vol. 41(3); 2001. p. 243.
/data/revues/00029378/v199i6sSA/S0002937808016608/ | 2011
Teresa Martino; Abimbola Aina-Mumuney; Maria Palmquist; Anadir Silva
Archive | 2007
D. Larma; Anadir Silva; Cynthia J. Holcroft; Richard E. Thompson; Pamela Donohue; Ernest M. Graham
American Journal of Obstetrics and Gynecology | 2006
Anadir Silva; Abimbola Aina-Mumuney
American Journal of Obstetrics and Gynecology | 2006
Anadir Silva; Joel Larma; Pamela K. Donohue; Cynthia J. Holcroft; Ernest Graham
American Journal of Obstetrics and Gynecology | 2005
Edith D. Gurewitsch; John C. Pezzullo; Anadir Silva; Shefali Agarwal; Sayeh Hamzehzadeh; Robert H. Allen
American Journal of Obstetrics and Gynecology | 2005
Anadir Silva; Alice Cootauco; Abimbola Aina-Mumuney; Pamela K. Donohue; Ernest Graham
American Journal of Obstetrics and Gynecology | 2004
Anadir Silva; Randi Smith; Christoph U. Lehmann; Cynthia J. Holcroft; Ernest Graham