Comparison between the perinatal risk inventory and the nursery neurobiological risk score for predicting development in high-risk newborn infants
Abstract Background The availability of a score for predicting neonatal outcome prior to discharge may help us to define the risk of developmental disorders in very low birth weight infants. Aim To compare Scheiner's Perinatal Risk Inventory (PERI) with Brazy's Neurobiological Risk Score (...
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description | Abstract Background The availability of a score for predicting neonatal outcome prior to discharge may help us to define the risk of developmental disorders in very low birth weight infants. Aim To compare Scheiner's Perinatal Risk Inventory (PERI) with Brazy's Neurobiological Risk Score (NBRS) when applied at discharge, in predicting developmental delay at 24 months of age. Study design To evaluate the predictive power of the two tests, we measured their sensitivity and specificity in predicting outcome (Mental Development Index, MDI, Psychomotor Development Index, PDI, and Amiel–Tison Neurological Examination) in an observational study. Subjects 102 very low birth weight infants (BW < 1500 g) admitted to our NICU at the Pediatric Department of Padova University. Results In the cohort studied, 75.5% of the patients had a normal MDI, while 24.5% showed a delayed performance (8.8% mildly and 15.7% severely so); the PDI was normal in 74.5% patients, whilst 25.5% had a delayed performance (9.8% mildly and 15.7% severely so). According to the Amiel–Tison test, neurological performance was normal in 66% patients, impaired without disability in 19% and impaired with disability in 15%. NBRS showed a sensitivity and specificity respectively of 0.96 and 0.23 (MDI), 0.96 and 0.24 (PDI), 0.94 and 0.25 (Amiel–Tison test); for PERI were 0.88 and 0.54 (MDI), 0.77 and 0.51 (PDI), 0.82 and 0.57 (Amiel–Tison test). The PERI and NBRS can predict the MDI with an AUC > 0.8 and the PDI or Amiel–Tison findings with an AUC of 0.7–0.8. No significant differences were found between the areas under the ROC curves using the NBRS and the PERI. Conclusions : In assessing the prognosis for individual babies, the physician can choose either the PERI or the NBRS to predict PDI, MDI or Amiel–Tison performance. |
doi_str_mv | 10.1016/j.earlhumdev.2007.08.003 |
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Aim To compare Scheiner's Perinatal Risk Inventory (PERI) with Brazy's Neurobiological Risk Score (NBRS) when applied at discharge, in predicting developmental delay at 24 months of age. Study design To evaluate the predictive power of the two tests, we measured their sensitivity and specificity in predicting outcome (Mental Development Index, MDI, Psychomotor Development Index, PDI, and Amiel–Tison Neurological Examination) in an observational study. Subjects 102 very low birth weight infants (BW < 1500 g) admitted to our NICU at the Pediatric Department of Padova University. Results In the cohort studied, 75.5% of the patients had a normal MDI, while 24.5% showed a delayed performance (8.8% mildly and 15.7% severely so); the PDI was normal in 74.5% patients, whilst 25.5% had a delayed performance (9.8% mildly and 15.7% severely so). According to the Amiel–Tison test, neurological performance was normal in 66% patients, impaired without disability in 19% and impaired with disability in 15%. NBRS showed a sensitivity and specificity respectively of 0.96 and 0.23 (MDI), 0.96 and 0.24 (PDI), 0.94 and 0.25 (Amiel–Tison test); for PERI were 0.88 and 0.54 (MDI), 0.77 and 0.51 (PDI), 0.82 and 0.57 (Amiel–Tison test). The PERI and NBRS can predict the MDI with an AUC > 0.8 and the PDI or Amiel–Tison findings with an AUC of 0.7–0.8. No significant differences were found between the areas under the ROC curves using the NBRS and the PERI. Conclusions : In assessing the prognosis for individual babies, the physician can choose either the PERI or the NBRS to predict PDI, MDI or Amiel–Tison performance.</description><identifier>ISSN: 0378-3782</identifier><identifier>EISSN: 1872-6232</identifier><identifier>DOI: 10.1016/j.earlhumdev.2007.08.003</identifier><identifier>PMID: 17897797</identifier><identifier>CODEN: EHDEDN</identifier><language>eng</language><publisher>Lausanne: Elsevier Ireland Ltd</publisher><subject>Advanced Basic Science ; Biological and medical sciences ; Child Development ; Cohort Studies ; Embryology: invertebrates and vertebrates. Teratology ; Fundamental and applied biological sciences. Psychology ; Humans ; Infant, Newborn ; Infant, Very Low Birth Weight - growth & development ; Intensive Care Units, Neonatal ; Neonatal and Perinatal Medicine ; Nursery neurobiological risk score ; Outcome ; Parents - education ; Perinatal risk inventory ; Risk ; Sensitivity and Specificity ; Very low birth weight infant</subject><ispartof>Early human development, 2008-05, Vol.84 (5), p.311-317</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2007 Elsevier Ireland Ltd</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c507t-dfafe0e03bd66ad01f3c8ff0869de0e9cb94863eb1120552e3e4f32171f33d243</citedby><cites>FETCH-LOGICAL-c507t-dfafe0e03bd66ad01f3c8ff0869de0e9cb94863eb1120552e3e4f32171f33d243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0378378207001454$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20353554$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17897797$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zaramella, Patrizia</creatorcontrib><creatorcontrib>Freato, Federica</creatorcontrib><creatorcontrib>Milan, Anna</creatorcontrib><creatorcontrib>Grisafi, Davide</creatorcontrib><creatorcontrib>Vianello, Andrea</creatorcontrib><creatorcontrib>Chiandetti, Lino</creatorcontrib><title>Comparison between the perinatal risk inventory and the nursery neurobiological risk score for predicting development in high-risk newborn infants</title><title>Early human development</title><addtitle>Early Hum Dev</addtitle><description>Abstract Background The availability of a score for predicting neonatal outcome prior to discharge may help us to define the risk of developmental disorders in very low birth weight infants. Aim To compare Scheiner's Perinatal Risk Inventory (PERI) with Brazy's Neurobiological Risk Score (NBRS) when applied at discharge, in predicting developmental delay at 24 months of age. Study design To evaluate the predictive power of the two tests, we measured their sensitivity and specificity in predicting outcome (Mental Development Index, MDI, Psychomotor Development Index, PDI, and Amiel–Tison Neurological Examination) in an observational study. Subjects 102 very low birth weight infants (BW < 1500 g) admitted to our NICU at the Pediatric Department of Padova University. Results In the cohort studied, 75.5% of the patients had a normal MDI, while 24.5% showed a delayed performance (8.8% mildly and 15.7% severely so); the PDI was normal in 74.5% patients, whilst 25.5% had a delayed performance (9.8% mildly and 15.7% severely so). According to the Amiel–Tison test, neurological performance was normal in 66% patients, impaired without disability in 19% and impaired with disability in 15%. NBRS showed a sensitivity and specificity respectively of 0.96 and 0.23 (MDI), 0.96 and 0.24 (PDI), 0.94 and 0.25 (Amiel–Tison test); for PERI were 0.88 and 0.54 (MDI), 0.77 and 0.51 (PDI), 0.82 and 0.57 (Amiel–Tison test). The PERI and NBRS can predict the MDI with an AUC > 0.8 and the PDI or Amiel–Tison findings with an AUC of 0.7–0.8. No significant differences were found between the areas under the ROC curves using the NBRS and the PERI. Conclusions : In assessing the prognosis for individual babies, the physician can choose either the PERI or the NBRS to predict PDI, MDI or Amiel–Tison performance.</description><subject>Advanced Basic Science</subject><subject>Biological and medical sciences</subject><subject>Child Development</subject><subject>Cohort Studies</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Infant, Very Low Birth Weight - growth & development</subject><subject>Intensive Care Units, Neonatal</subject><subject>Neonatal and Perinatal Medicine</subject><subject>Nursery neurobiological risk score</subject><subject>Outcome</subject><subject>Parents - education</subject><subject>Perinatal risk inventory</subject><subject>Risk</subject><subject>Sensitivity and Specificity</subject><subject>Very low birth weight infant</subject><issn>0378-3782</issn><issn>1872-6232</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks2O0zAUhSMEYsrAKyBvYJdwbefH2SBBxZ80EgtgbTnOdetOYgc76aivwRPjTAsjsWJhWb7-fHx0z80yQqGgQOs3hwJVGPbL2OOxYABNAaIA4I-yDRUNy2vG2eNsA7wReVrsKnsW4wEAKtHC0-yKNqJtmrbZZL-2fpxUsNE70uF8h-jIvEcyYbBOzWog6e6WWHdEN_twIsr194BbQsR0drgE31k_-J3Vf_CofUBifCBTwN7q2bodSV5x8NOYhJIe2dvdPr-nHd51PrhUNMrN8Xn2xKgh4ovLfp39-Pjh-_ZzfvP105ftu5tcV9DMeW-UQUDgXV_XqgdquBbGgKjbPtVb3bWlqDl2lDKoKoYcS8MZbRLIe1by6-z1WXcK_ueCcZajjRqHQTn0S5R1SwUvqzaB4gzq4GMMaOQU7KjCSVKQax7yIB_ykGseEoRMeaSnLy9_LN2I_cPDSwAJeHUBVEztM0E5beNfjgGveFWtZt-fOUwdOVoMMmqLTqfuBtSz7L39Hzdv_xHRg3VrbLd4wnjwS3Cp45LKyCTIb-v8rOMDDQAtk4vfGGLIBA</recordid><startdate>20080501</startdate><enddate>20080501</enddate><creator>Zaramella, Patrizia</creator><creator>Freato, Federica</creator><creator>Milan, Anna</creator><creator>Grisafi, Davide</creator><creator>Vianello, Andrea</creator><creator>Chiandetti, Lino</creator><general>Elsevier Ireland Ltd</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>20080501</creationdate><title>Comparison between the perinatal risk inventory and the nursery neurobiological risk score for predicting development in high-risk newborn infants</title><author>Zaramella, Patrizia ; Freato, Federica ; Milan, Anna ; Grisafi, Davide ; Vianello, Andrea ; Chiandetti, Lino</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c507t-dfafe0e03bd66ad01f3c8ff0869de0e9cb94863eb1120552e3e4f32171f33d243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Advanced Basic Science</topic><topic>Biological and medical sciences</topic><topic>Child Development</topic><topic>Cohort Studies</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Infant, Very Low Birth Weight - growth & development</topic><topic>Intensive Care Units, Neonatal</topic><topic>Neonatal and Perinatal Medicine</topic><topic>Nursery neurobiological risk score</topic><topic>Outcome</topic><topic>Parents - education</topic><topic>Perinatal risk inventory</topic><topic>Risk</topic><topic>Sensitivity and Specificity</topic><topic>Very low birth weight infant</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zaramella, Patrizia</creatorcontrib><creatorcontrib>Freato, Federica</creatorcontrib><creatorcontrib>Milan, Anna</creatorcontrib><creatorcontrib>Grisafi, Davide</creatorcontrib><creatorcontrib>Vianello, Andrea</creatorcontrib><creatorcontrib>Chiandetti, Lino</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>Early human development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zaramella, Patrizia</au><au>Freato, Federica</au><au>Milan, Anna</au><au>Grisafi, Davide</au><au>Vianello, Andrea</au><au>Chiandetti, Lino</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison between the perinatal risk inventory and the nursery neurobiological risk score for predicting development in high-risk newborn infants</atitle><jtitle>Early human development</jtitle><addtitle>Early Hum Dev</addtitle><date>2008-05-01</date><risdate>2008</risdate><volume>84</volume><issue>5</issue><spage>311</spage><epage>317</epage><pages>311-317</pages><issn>0378-3782</issn><eissn>1872-6232</eissn><coden>EHDEDN</coden><abstract>Abstract Background The availability of a score for predicting neonatal outcome prior to discharge may help us to define the risk of developmental disorders in very low birth weight infants. Aim To compare Scheiner's Perinatal Risk Inventory (PERI) with Brazy's Neurobiological Risk Score (NBRS) when applied at discharge, in predicting developmental delay at 24 months of age. Study design To evaluate the predictive power of the two tests, we measured their sensitivity and specificity in predicting outcome (Mental Development Index, MDI, Psychomotor Development Index, PDI, and Amiel–Tison Neurological Examination) in an observational study. Subjects 102 very low birth weight infants (BW < 1500 g) admitted to our NICU at the Pediatric Department of Padova University. Results In the cohort studied, 75.5% of the patients had a normal MDI, while 24.5% showed a delayed performance (8.8% mildly and 15.7% severely so); the PDI was normal in 74.5% patients, whilst 25.5% had a delayed performance (9.8% mildly and 15.7% severely so). According to the Amiel–Tison test, neurological performance was normal in 66% patients, impaired without disability in 19% and impaired with disability in 15%. NBRS showed a sensitivity and specificity respectively of 0.96 and 0.23 (MDI), 0.96 and 0.24 (PDI), 0.94 and 0.25 (Amiel–Tison test); for PERI were 0.88 and 0.54 (MDI), 0.77 and 0.51 (PDI), 0.82 and 0.57 (Amiel–Tison test). The PERI and NBRS can predict the MDI with an AUC > 0.8 and the PDI or Amiel–Tison findings with an AUC of 0.7–0.8. No significant differences were found between the areas under the ROC curves using the NBRS and the PERI. Conclusions : In assessing the prognosis for individual babies, the physician can choose either the PERI or the NBRS to predict PDI, MDI or Amiel–Tison performance.</abstract><cop>Lausanne</cop><cop>New York,NY</cop><cop>Amsterdam</cop><pub>Elsevier Ireland Ltd</pub><pmid>17897797</pmid><doi>10.1016/j.earlhumdev.2007.08.003</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Advanced Basic Science Biological and medical sciences Child Development Cohort Studies Embryology: invertebrates and vertebrates. Teratology Fundamental and applied biological sciences. Psychology Humans Infant, Newborn Infant, Very Low Birth Weight - growth & development Intensive Care Units, Neonatal Neonatal and Perinatal Medicine Nursery neurobiological risk score Outcome Parents - education Perinatal risk inventory Risk Sensitivity and Specificity Very low birth weight infant |
title | Comparison between the perinatal risk inventory and the nursery neurobiological risk score for predicting development in high-risk newborn infants |
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