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1.
Arch Dis Child Fetal Neonatal Ed ; 82(2): F141-4, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10685988

ABSTRACT

OBJECTIVE: To elucidate clinical antecedents of sensorineural hearing loss (SNHL) in very preterm infants. DESIGN: Case-control study. SUBJECTS: Fifteen children < 33 weeks' gestation with significant SNHL born between 1 January 1990 and 31 December 1994, detected within 9 months of birth, and 30 matched control children. METHODOLOGY: Perinatal variables in the two groups were compared using non-parametric tests and conditional logistic regression (EGRET). RESULTS: Median birth weight for the index group was 960 g (range 600-2914 g) compared with 1026 g (range 410-2814 g) for controls. Children with SNHL had longer periods of intubation, ventilation, oxygen treatment, and acidosis, and more frequent treatment with dopamine or frusemide. Neither peak nor trough aminoglycoside levels, nor duration of jaundice or level of bilirubin varied between groups. However, SNHL was more likely if peak bilirubin levels coexisted with netilmicin use (odds ratio (95% confidence interval) 14.2 (1.8 to 113.6)) or if acidosis occurred when bilirubin levels were over 200 micromol/l (OR 8.0 (0.9 to 71.6). Frusemide use in the face of high serum creatinine levels (OR 8.9 (1.1 to 74.5)) or netilmicin treatment (OR 5.0 (0.99 to 24.8)) was also associated with SNHL. At 12 months of age, seven of 15 children with SNHL had evidence of cerebral palsy compared with two of 30 controls (OR 12.3 (2.1 to 71)). CONCLUSIONS: Preterm children with SNHL required more intensive care in the perinatal period and developed more neurological complications than controls. Among very preterm babies, the coexistence of risk factors for hearing loss may be more important than the individual factors themselves.


Subject(s)
Hearing Loss, Sensorineural/etiology , Infant, Premature , Aminoglycosides/blood , Bilirubin/blood , Case-Control Studies , Data Collection , Female , Humans , Infant, Newborn , Intensive Care, Neonatal , Intubation/adverse effects , Logistic Models , Male , Risk Factors
5.
Int J Radiat Oncol Biol Phys ; 19(3): 665-8, 1990 Sep.
Article in English | MEDLINE | ID: mdl-2211213

ABSTRACT

Normal tissue effects in mice due to combinations of a perfluorochemical emulsion, Fluosol-DA 20%, 100% oxygen, and whole-body irradiation were investigated. Eight-to-10-week-old C57BL/6 male mice were injected via the tail vein with 10 ml/kg of Fluosol-DA with and without subsequent exposure to oxygen for 60 minutes. Animals then received graded doses of whole-body radiation (4 MV photons) at a dose rate of 2.85 +/- .015 Gy/minute. Using linear regression analysis, the lethal doses of radiation to 50% and 10% of the animals within 30 days in the absence of Fluosol-DA and oxygen were 8.35 Gy (95% c.l.:7.77-8.93 Gy) and 6.73 Gy (95% cl.:6.21-7.25 Gy), respectively, and were unaffected by Fluosol-DA and/or oxygen pre-treatment. However, Fluosol-DA given alone or in combination with oxygen produced increased balding and decreased graying incidence in mice within 60 days, and resulted in depressed weight gain 15 to 60 days post-treatment. Normal tissue effects due to administration of Fluosol-DA and oxygen in combination with whole-body irradiation have been demonstrated but appear minimal compared to other anti-tumor modalities currently under investigation.


Subject(s)
Fluorocarbons/pharmacology , Oxygen/pharmacology , Radiation-Sensitizing Agents/pharmacology , Whole-Body Irradiation , Alopecia/etiology , Animals , Body Weight/drug effects , Body Weight/radiation effects , Drug Combinations , Hair Color/drug effects , Hair Color/radiation effects , Hydroxyethyl Starch Derivatives , Male , Mice , Mice, Inbred C57BL
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