8 research outputs found

    Deficiencies according to gestational age and neonatal cerebral lesions.

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    (1)<p>inclusion 1997+1998.</p>(2)<p>inclusion 1997.</p>(3)<p>Major : cystic PVL or IPH, Moderate : persistent echodensities or ventricular dilatation or grade III IVH, Minor : grade II and grade I IVH (1 missing neonatal cerebral lesion information in the group of 24–26 SA and 32 missing in the groups 29–32 SA).</p

    Flow diagram of case selection.

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    <p>(N)ICU, (neonatal) intensive care unit; CoNS, coagulase-negative staphylococci; BC, blood culture. <sup>a</sup>In NICU infants, a single CoNS-positive blood culture was interpreted as possible bacteremia and included in the analysis. The CoNS-positive results that were excluded were explicitly recorded as a contaminant in the microbiology record. <sup>b</sup>In adult patients, a single CoNS-positive blood culture was interpreted as a contaminant and excluded from the analysis. <sup>c</sup>Records were excluded when antimicrobial susceptibility results were not available.</p

    <i>Staphylococcus capitis</i> isolates from distant neonatal intensive care units (NICUs) are clonal.

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    <p>Pulsed-field gel electrophoresis (PFGE) was applied to 53 bloodstream isolates of <i>S. capitis</i> that were collected from NICU infants and adult patients from cities spanning the French territory. The PFGE dendrogram was generated using the GelCompar software version 4.1. The isolates were assigned to pulsotypes using >80% similarity (vertical dashed line). Staphylococcal chromosomal cassette <i>mec</i> (SCC<i>mec</i>) typing was applied to 23 methicillin-resistant isolates representative of each pulsotype and geographic origin. All methicillin-resistant isolates from the different NICUs belonged to the same pulsotype and shared a type V-related SCC<i>mec</i> element, whereas methicillin-susceptible and/or non-NICU isolates were genetically diverse. <i>ccr</i>, chromosomal cassette recombinase; unkn., unknown (a combination of the <i>mec</i> complex and <i>ccr</i> genes has not been assigned to an SCC<i>mec</i> type so far).</p

    Classification of deficiencies.<sup>(1)</sup>

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    (1)<p>For each deficiency, the classification follows a priority order according to severity at the most recent step of the follow-up available.</p>(2)<p>Moderate Neuromotor Dysfunction (MND-2) at the short version of the Touwen neurological examination at the age of 5 years <sup>11.</sup></p>(3)<p>Including children free of CP or other neuromotor disorders but who were not assessed with the Touwen examination.</p>(4)<p>Except for visual or hearing deficiency only; for 25 children in special school/class at 8 years of age with MPC at 5 years ≥70 or missing, other data in their record allowed us to classify 14 with a severe cognitive deficiency, 10 with moderate, and 1 with none identified record allowed to classify 14 as severe crecords.</p>(5)<p>MPC = Mental Processing Composite of the K-ABC test <sup>14.</sup></p>(6)<p>MDPH = Maisons départementales des Personnes handicapées.</p>(7)<p>Regardless of all other deficiencies.</p
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