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dc.contributor.authorKahn, Doron J.
dc.contributor.authorRichardson, Douglas K.
dc.contributor.authorBillett, Henny H.
dc.contributor.authorBednarek, Francis J.
dc.contributor.authorWeisberger, Stuart
dc.date2022-08-11T08:10:12.000
dc.date.accessioned2022-08-23T16:59:07Z
dc.date.available2022-08-23T16:59:07Z
dc.date.issued2003-06-01
dc.date.submitted2012-05-02
dc.identifier.citationJ Perinatol. 2003 Jun;23(4):312-6. <a href="http://dx.doi.org/10.1038/sj.jp.7210910">Link to article on publisher's site</a>
dc.identifier.issn0743-8346 (Linking)
dc.identifier.doi10.1038/sj.jp.7210910
dc.identifier.pmid12774140
dc.identifier.urihttp://hdl.handle.net/20.500.14038/43514
dc.description<p>Francis Bednarek and Stuart Weisberger are co-investigators in the SNAP II Study Group.</p>
dc.description.abstractOBJECTIVES: To investigate variation among neonatal intensive care units (NICUs) in prevalence and management of thrombocytopenia in infants and(SNAP). Platelet counts in the first 12 hours after birth and on day 3 of life were abstracted from the infants' medical records. Thrombocytopenia was determined from the lowest platelet count in each of these time periods. RESULTS: There was variability in rates of thrombocytopenia among NICUs, even after controlling for risk factors (e.g., SNAP, small for gestational (SGA) age and maternal hypertension). One site had a high prevalence of thrombocytopenia, but the lowest percentage of infants with thrombocytopenia who received platelet transfusions. After controlling for SNAP, GA, SGA, Apgar score and incidence of thrombocytopenia, the odds of receiving platelets at this site, relative to the site with the highest transfusion rate, was 0.10 (95% CI 0.02 to 0.43). CONCLUSIONS: This multicenter study finds a 10-fold variation among NICU in the administration of platelets to their thrombocytopenic infants that cannot be explained by presence of thrombocytopenia or illness severity.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=12774140&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1038/sj.jp.7210910
dc.subjectCohort Studies; Humans; Infant, Newborn; *Infant, Very Low Birth Weight; Intensive Care Units, Neonatal; Intracranial Hemorrhages; Physician's Practice Patterns; *Platelet Transfusion; Prevalence; Prospective Studies; Severity of Illness Index; Thrombocytopenia; Treatment Outcome
dc.subjectPediatrics
dc.titleInter-NICU variation in rates and management of thrombocytopenia among very low birth-weight infants
dc.typeJournal Article
dc.source.journaltitleJournal of perinatology : official journal of the California Perinatal Association
dc.source.volume23
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/peds_neonatology/8
dc.identifier.contextkey2816714
html.description.abstract<p>OBJECTIVES: To investigate variation among neonatal intensive care units (NICUs) in prevalence and management of thrombocytopenia in infants and(SNAP). Platelet counts in the first 12 hours after birth and on day 3 of life were abstracted from the infants' medical records. Thrombocytopenia was determined from the lowest platelet count in each of these time periods.</p> <p>RESULTS: There was variability in rates of thrombocytopenia among NICUs, even after controlling for risk factors (e.g., SNAP, small for gestational (SGA) age and maternal hypertension). One site had a high prevalence of thrombocytopenia, but the lowest percentage of infants with thrombocytopenia who received platelet transfusions. After controlling for SNAP, GA, SGA, Apgar score and incidence of thrombocytopenia, the odds of receiving platelets at this site, relative to the site with the highest transfusion rate, was 0.10 (95% CI 0.02 to 0.43).</p> <p>CONCLUSIONS: This multicenter study finds a 10-fold variation among NICU in the administration of platelets to their thrombocytopenic infants that cannot be explained by presence of thrombocytopenia or illness severity.</p>
dc.identifier.submissionpathpeds_neonatology/8
dc.contributor.departmentDepartment of Pediatrics
dc.source.pages312-6


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