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Nucleated red blood cell counts in the first week of life: a critical appraisal of relationships with perinatal outcome in preterm growth-restricted neonates
Objective Nucleated red blood cells (NRBC) are fetal hematologic markers for placental dysfunction, hypoxemia, and asphyxia. NRBC count elevation at birth or persistence is linked statistically to adverse outcome, but clinical predictive value is variable. We studied novel indices to better define o...
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Published in: | American journal of obstetrics and gynecology 2007-09, Vol.197 (3), p.286.e1-286.e8 |
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container_title | American journal of obstetrics and gynecology |
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description | Objective Nucleated red blood cells (NRBC) are fetal hematologic markers for placental dysfunction, hypoxemia, and asphyxia. NRBC count elevation at birth or persistence is linked statistically to adverse outcome, but clinical predictive value is variable. We studied novel indices to better define overall magnitude of NRBC response. Study Design Peripheral NRBC count was obtained from preterm (30/100 white blood cells were determined. Mean counts (NRBC-mean), area under the curve (NRBC-AUC), and declination (NRBC-slope) were analyzed over week 1. NRBC parameters were related to major morbidity (bronchopulmonary dysplasia, grade III/IV intraventricular hemorrhage, necrotizing enterocolitis included) and neonatal death (NND). Results Twenty-two of 176 patients (12.5%) had acidosis. Complications included bronchopulmonary dysplasia (n = 36; 20.5%), intraventricular hemorrhage (n = 18; 10.2%), necrotizing enterocolitis (n = 18; 10.2%), NND (n = 18; 10.2%). NRBC-AUC and NRBC-mean correlated most strongly with pH, birthweight, and gestational age (Pearson coefficien,t −0.45 to −0.18; all P < .001). NRBC-AUC varied most between nonmorbid and morbid; NRBC-mean varied most between survivors and NND (all P < .001). NRBC persistence strongly predicted NND: clearance by day 4 was achieved by 80% of survivors and only 35% of NNDs. Logistic regression identified prematurity and persistent NRBC counts as primary morbidity determinants (r2 = 0.56; P < .01). Although the importance of individual NRBC counts varied, day-4 NRBC counts of >70 predicted morbidity best (sensitivity, 82%; specificity, 96%). Presence of morbidity and birthweight were prime determinants of death (r2 = 0.42; P < .01). Conclusion Simple daily NRBC counts provide clinical information that is equivalent to more complicated methods. The importance of prematurity and growth are emphasized, but elevated NRBC counts beyond day 3 are relevant independent predictors of adverse outcome. |
doi_str_mv | 10.1016/j.ajog.2007.06.020 |
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NRBC count elevation at birth or persistence is linked statistically to adverse outcome, but clinical predictive value is variable. We studied novel indices to better define overall magnitude of NRBC response. Study Design Peripheral NRBC count was obtained from preterm (<34 weeks of gestation) growth-restricted neonates within 2 hours of life. Daily counts and duration of NRBC count >30/100 white blood cells were determined. Mean counts (NRBC-mean), area under the curve (NRBC-AUC), and declination (NRBC-slope) were analyzed over week 1. NRBC parameters were related to major morbidity (bronchopulmonary dysplasia, grade III/IV intraventricular hemorrhage, necrotizing enterocolitis included) and neonatal death (NND). Results Twenty-two of 176 patients (12.5%) had acidosis. Complications included bronchopulmonary dysplasia (n = 36; 20.5%), intraventricular hemorrhage (n = 18; 10.2%), necrotizing enterocolitis (n = 18; 10.2%), NND (n = 18; 10.2%). NRBC-AUC and NRBC-mean correlated most strongly with pH, birthweight, and gestational age (Pearson coefficien,t −0.45 to −0.18; all P < .001). NRBC-AUC varied most between nonmorbid and morbid; NRBC-mean varied most between survivors and NND (all P < .001). NRBC persistence strongly predicted NND: clearance by day 4 was achieved by 80% of survivors and only 35% of NNDs. Logistic regression identified prematurity and persistent NRBC counts as primary morbidity determinants (r2 = 0.56; P < .01). Although the importance of individual NRBC counts varied, day-4 NRBC counts of >70 predicted morbidity best (sensitivity, 82%; specificity, 96%). Presence of morbidity and birthweight were prime determinants of death (r2 = 0.42; P < .01). Conclusion Simple daily NRBC counts provide clinical information that is equivalent to more complicated methods. The importance of prematurity and growth are emphasized, but elevated NRBC counts beyond day 3 are relevant independent predictors of adverse outcome.</description><identifier>ISSN: 0002-9378</identifier><identifier>EISSN: 1097-6868</identifier><identifier>DOI: 10.1016/j.ajog.2007.06.020</identifier><identifier>PMID: 17826423</identifier><identifier>CODEN: AJOGAH</identifier><language>eng</language><publisher>Philadelphia, PA: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Erythroblasts ; Erythrocyte Count ; Female ; Fetal Growth Retardation - physiopathology ; fetus ; growth restriction ; Gynecology. Andrology. Obstetrics ; Humans ; Infant, Newborn ; Infant, Newborn, Diseases - epidemiology ; Infant, Newborn, Diseases - etiology ; Infant, Newborn, Diseases - physiopathology ; Infant, Premature - blood ; Medical sciences ; nucleated red blood cells ; Obstetrics and Gynecology ; perinatal outcome ; Placenta Diseases - diagnostic imaging ; Predictive Value of Tests ; Pregnancy ; Prospective Studies ; Ultrasonography</subject><ispartof>American journal of obstetrics and gynecology, 2007-09, Vol.197 (3), p.286.e1-286.e8</ispartof><rights>Mosby, Inc.</rights><rights>2007 Mosby, Inc.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-113417d047a1154c8420a892b5bc240e808d7109d3a9145d057dfbe4049fb8b13</citedby><cites>FETCH-LOGICAL-c439t-113417d047a1154c8420a892b5bc240e808d7109d3a9145d057dfbe4049fb8b13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19865532$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17826423$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baschat, Ahmet A., MD</creatorcontrib><creatorcontrib>Gungor, Sadettin, MD</creatorcontrib><creatorcontrib>Kush, Michelle L., MD</creatorcontrib><creatorcontrib>Berg, Christoph, MD</creatorcontrib><creatorcontrib>Gembruch, Ulrich, MD</creatorcontrib><creatorcontrib>Harman, Christopher R., MD</creatorcontrib><title>Nucleated red blood cell counts in the first week of life: a critical appraisal of relationships with perinatal outcome in preterm growth-restricted neonates</title><title>American journal of obstetrics and gynecology</title><addtitle>Am J Obstet Gynecol</addtitle><description>Objective Nucleated red blood cells (NRBC) are fetal hematologic markers for placental dysfunction, hypoxemia, and asphyxia. NRBC count elevation at birth or persistence is linked statistically to adverse outcome, but clinical predictive value is variable. We studied novel indices to better define overall magnitude of NRBC response. Study Design Peripheral NRBC count was obtained from preterm (<34 weeks of gestation) growth-restricted neonates within 2 hours of life. Daily counts and duration of NRBC count >30/100 white blood cells were determined. Mean counts (NRBC-mean), area under the curve (NRBC-AUC), and declination (NRBC-slope) were analyzed over week 1. NRBC parameters were related to major morbidity (bronchopulmonary dysplasia, grade III/IV intraventricular hemorrhage, necrotizing enterocolitis included) and neonatal death (NND). Results Twenty-two of 176 patients (12.5%) had acidosis. Complications included bronchopulmonary dysplasia (n = 36; 20.5%), intraventricular hemorrhage (n = 18; 10.2%), necrotizing enterocolitis (n = 18; 10.2%), NND (n = 18; 10.2%). NRBC-AUC and NRBC-mean correlated most strongly with pH, birthweight, and gestational age (Pearson coefficien,t −0.45 to −0.18; all P < .001). NRBC-AUC varied most between nonmorbid and morbid; NRBC-mean varied most between survivors and NND (all P < .001). NRBC persistence strongly predicted NND: clearance by day 4 was achieved by 80% of survivors and only 35% of NNDs. Logistic regression identified prematurity and persistent NRBC counts as primary morbidity determinants (r2 = 0.56; P < .01). Although the importance of individual NRBC counts varied, day-4 NRBC counts of >70 predicted morbidity best (sensitivity, 82%; specificity, 96%). Presence of morbidity and birthweight were prime determinants of death (r2 = 0.42; P < .01). Conclusion Simple daily NRBC counts provide clinical information that is equivalent to more complicated methods. The importance of prematurity and growth are emphasized, but elevated NRBC counts beyond day 3 are relevant independent predictors of adverse outcome.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Erythroblasts</subject><subject>Erythrocyte Count</subject><subject>Female</subject><subject>Fetal Growth Retardation - physiopathology</subject><subject>fetus</subject><subject>growth restriction</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Infant, Newborn, Diseases - epidemiology</subject><subject>Infant, Newborn, Diseases - etiology</subject><subject>Infant, Newborn, Diseases - physiopathology</subject><subject>Infant, Premature - blood</subject><subject>Medical sciences</subject><subject>nucleated red blood cells</subject><subject>Obstetrics and Gynecology</subject><subject>perinatal outcome</subject><subject>Placenta Diseases - diagnostic imaging</subject><subject>Predictive Value of Tests</subject><subject>Pregnancy</subject><subject>Prospective Studies</subject><subject>Ultrasonography</subject><issn>0002-9378</issn><issn>1097-6868</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp9ks-K1TAUxoMoznX0BVxINrprPUnTNhURZPAfDLpQ1yFNT-em09vUJPUyD-O7mnAvDLhwEZJwfufj8H2HkOcMSgaseT2VenI3JQdoS2hK4PCA7Bh0bdHIRj4kOwDgRVe18oI8CWHKX97xx-SCtZI3glc78ufrZmbUEQfq0-ln5wZqcJ6pcdsSA7ULjXuko_Uh0iPiLXUjne2Ib6imxttojZ6pXlevbUivVPU462jdEvZ2DfRo456u6O2iY65v0bgDZt3VY0R_oDfeHeO-8BiityaPsqBLNIan5NGo54DPzvcl-fnxw4-rz8X1t09frt5fF0ZUXSwYqwRrBxCtZqwWRgoOWna8r3vDBaAEObTJmKHSHRP1AHU7jD0KEN3Yy55Vl-TVSXf17teW5lAHG7ILOk2yBdVILrpGZJCfQONdCB5HtXp70P5OMVA5FDWpHIrKoShoVAolNb04q2_9AYf7lnMKCXh5BnRIbo5eL8aGe66TTV1XPHFvTxwmL35b9CoYi4vBwXo0UQ3O_n-Od_-0m9kuOb9bvMMwuc0vyWXFVOAK1Pe8L3l7oE0iomPVX7Dmwcs</recordid><startdate>20070901</startdate><enddate>20070901</enddate><creator>Baschat, Ahmet A., MD</creator><creator>Gungor, Sadettin, MD</creator><creator>Kush, Michelle L., MD</creator><creator>Berg, Christoph, MD</creator><creator>Gembruch, Ulrich, MD</creator><creator>Harman, Christopher R., MD</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20070901</creationdate><title>Nucleated red blood cell counts in the first week of life: a critical appraisal of relationships with perinatal outcome in preterm growth-restricted neonates</title><author>Baschat, Ahmet A., MD ; Gungor, Sadettin, MD ; Kush, Michelle L., MD ; Berg, Christoph, MD ; Gembruch, Ulrich, MD ; Harman, Christopher R., MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-113417d047a1154c8420a892b5bc240e808d7109d3a9145d057dfbe4049fb8b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Erythroblasts</topic><topic>Erythrocyte Count</topic><topic>Female</topic><topic>Fetal Growth Retardation - physiopathology</topic><topic>fetus</topic><topic>growth restriction</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Infant, Newborn, Diseases - epidemiology</topic><topic>Infant, Newborn, Diseases - etiology</topic><topic>Infant, Newborn, Diseases - physiopathology</topic><topic>Infant, Premature - blood</topic><topic>Medical sciences</topic><topic>nucleated red blood cells</topic><topic>Obstetrics and Gynecology</topic><topic>perinatal outcome</topic><topic>Placenta Diseases - diagnostic imaging</topic><topic>Predictive Value of Tests</topic><topic>Pregnancy</topic><topic>Prospective Studies</topic><topic>Ultrasonography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baschat, Ahmet A., MD</creatorcontrib><creatorcontrib>Gungor, Sadettin, MD</creatorcontrib><creatorcontrib>Kush, Michelle L., MD</creatorcontrib><creatorcontrib>Berg, Christoph, MD</creatorcontrib><creatorcontrib>Gembruch, Ulrich, MD</creatorcontrib><creatorcontrib>Harman, Christopher R., MD</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of obstetrics and gynecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baschat, Ahmet A., MD</au><au>Gungor, Sadettin, MD</au><au>Kush, Michelle L., MD</au><au>Berg, Christoph, MD</au><au>Gembruch, Ulrich, MD</au><au>Harman, Christopher R., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nucleated red blood cell counts in the first week of life: a critical appraisal of relationships with perinatal outcome in preterm growth-restricted neonates</atitle><jtitle>American journal of obstetrics and gynecology</jtitle><addtitle>Am J Obstet Gynecol</addtitle><date>2007-09-01</date><risdate>2007</risdate><volume>197</volume><issue>3</issue><spage>286.e1</spage><epage>286.e8</epage><pages>286.e1-286.e8</pages><issn>0002-9378</issn><eissn>1097-6868</eissn><coden>AJOGAH</coden><abstract>Objective Nucleated red blood cells (NRBC) are fetal hematologic markers for placental dysfunction, hypoxemia, and asphyxia. NRBC count elevation at birth or persistence is linked statistically to adverse outcome, but clinical predictive value is variable. We studied novel indices to better define overall magnitude of NRBC response. Study Design Peripheral NRBC count was obtained from preterm (<34 weeks of gestation) growth-restricted neonates within 2 hours of life. Daily counts and duration of NRBC count >30/100 white blood cells were determined. Mean counts (NRBC-mean), area under the curve (NRBC-AUC), and declination (NRBC-slope) were analyzed over week 1. NRBC parameters were related to major morbidity (bronchopulmonary dysplasia, grade III/IV intraventricular hemorrhage, necrotizing enterocolitis included) and neonatal death (NND). Results Twenty-two of 176 patients (12.5%) had acidosis. Complications included bronchopulmonary dysplasia (n = 36; 20.5%), intraventricular hemorrhage (n = 18; 10.2%), necrotizing enterocolitis (n = 18; 10.2%), NND (n = 18; 10.2%). NRBC-AUC and NRBC-mean correlated most strongly with pH, birthweight, and gestational age (Pearson coefficien,t −0.45 to −0.18; all P < .001). NRBC-AUC varied most between nonmorbid and morbid; NRBC-mean varied most between survivors and NND (all P < .001). NRBC persistence strongly predicted NND: clearance by day 4 was achieved by 80% of survivors and only 35% of NNDs. Logistic regression identified prematurity and persistent NRBC counts as primary morbidity determinants (r2 = 0.56; P < .01). Although the importance of individual NRBC counts varied, day-4 NRBC counts of >70 predicted morbidity best (sensitivity, 82%; specificity, 96%). Presence of morbidity and birthweight were prime determinants of death (r2 = 0.42; P < .01). Conclusion Simple daily NRBC counts provide clinical information that is equivalent to more complicated methods. The importance of prematurity and growth are emphasized, but elevated NRBC counts beyond day 3 are relevant independent predictors of adverse outcome.</abstract><cop>Philadelphia, PA</cop><pub>Elsevier Inc</pub><pmid>17826423</pmid><doi>10.1016/j.ajog.2007.06.020</doi><tpages>3</tpages></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Erythroblasts Erythrocyte Count Female Fetal Growth Retardation - physiopathology fetus growth restriction Gynecology. Andrology. Obstetrics Humans Infant, Newborn Infant, Newborn, Diseases - epidemiology Infant, Newborn, Diseases - etiology Infant, Newborn, Diseases - physiopathology Infant, Premature - blood Medical sciences nucleated red blood cells Obstetrics and Gynecology perinatal outcome Placenta Diseases - diagnostic imaging Predictive Value of Tests Pregnancy Prospective Studies Ultrasonography |
title | Nucleated red blood cell counts in the first week of life: a critical appraisal of relationships with perinatal outcome in preterm growth-restricted neonates |
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