نمایش مختصر رکورد

dc.contributor.authorMohammadzadeh, Ashrafen_US
dc.contributor.authorFarhat, Ahmadshahen_US
dc.contributor.authorGhasemian, Ahmaden_US
dc.contributor.authorRamezani, Mohammaden_US
dc.contributor.authorEsmaily, Habibullahen_US
dc.contributor.authorMusavi, Bibi Marziyehen_US
dc.date.accessioned1399-07-09T07:30:19Zfa_IR
dc.date.accessioned2020-09-30T07:30:19Z
dc.date.available1399-07-09T07:30:19Zfa_IR
dc.date.available2020-09-30T07:30:19Z
dc.date.issued2016-06-01en_US
dc.date.issued1395-03-12fa_IR
dc.date.submitted2015-11-06en_US
dc.date.submitted1394-08-15fa_IR
dc.identifier.citationMohammadzadeh, Ashraf, Farhat, Ahmadshah, Ghasemian, Ahmad, Ramezani, Mohammad, Esmaily, Habibullah, Musavi, Bibi Marziyeh. (2016). Effects of oral zinc sulfate on hyperbilirubinemia in low-birth-weight neonates. Iranian Journal of Neonatology IJN, 7(2), 11-15. doi: 10.22038/ijn.2016.7107en_US
dc.identifier.issn2251-7510
dc.identifier.issn2322-2158
dc.identifier.urihttps://dx.doi.org/10.22038/ijn.2016.7107
dc.identifier.urihttp://ijn.mums.ac.ir/article_7107.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/323231
dc.description.abstract<strong><em>Background</em></strong><strong>:</strong> Hyperbilirubinemia is one of the most common and persistent problems encountered in preterm newborns. This condition in preterm infant is more likely to be associated with neurological damage rather than terms. So far, no major studies have precisely assessed the effects of zinc sulfate on hyperbilirubinemia in low-birth-weight (LBW) neonates. Therefore, in this study, we aimed to evaluate these effects in LBW infants. <strong><em>Methods</em></strong><strong>:</strong> This randomized, double-blind, clinical trial (IRCT201401041162N22) was performed on 61 icteric LBW neonates, hospitalized in the neonatal intensive care unit (NICU) of Imam Reza Hospital in Mashhad, Iran from May 24, 2014 to May 24, 2015. The neonates were randomly divided into case and control groups, and the total serum bilirubin (TSB) level was measured at 0, 24, 48, 72, 96, and 120 h after treatment. The subjects received either 10 mg of zinc sulfate or placebo twice per day for five days (or by the end of treatment). The termination point of phototherapy was defined as a bilirubin level below 50% of the starting point. The collected data were analyzed, using SPSS version 20. Chi-square, t-test, and repeated measures ANOVA were carried out to compare the findings between the two groups. <strong><em>Results</em></strong><strong>:</strong> The mean TSB level was 14.87±2.65 and 14.73±3.22 mg/dl in the control and case groups. The mean decline in TSB level was only significant at 24 h after the treatment (2.71 and 2.13 mg/dl in the case and control groups, respectively; P=0.04), while being statistically insignificant on other days of the assessment. Also, similar findings were reported regarding the duration of treatment in the case and control groups (58.84±14.97 and 65.60±16.59 h in the case and control groups, respectively). <strong><em>Conclusion:</em></strong> The present study showed that administration of oral zinc sulfate in icteric LBW infants could significantly reduce TSB level only at 24 h following the treatment.en_US
dc.format.extent1410
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Neonatology IJNen_US
dc.relation.isversionofhttps://dx.doi.org/10.22038/ijn.2016.7107
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dc.titleEffects of oral zinc sulfate on hyperbilirubinemia in low-birth-weight neonatesen_US
dc.typeTexten_US
dc.typeOriginal Articleen_US
dc.contributor.departmentNeonatal Research Center, Imam Reza Hospital, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentNeonatal Research Center, Imam Reza Hospital, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentHealth Science Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentPharmaceutical and Biotechnology Research Center, Faculty of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentHealth Science Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iranen_US
dc.contributor.departmentNurse, health educator, Mashhad education center, Mashhad, Iran.en_US
dc.citation.volume7
dc.citation.issue2
dc.citation.spage11
dc.citation.epage15
nlai.contributor.orcid0000-0001-2345-6789
nlai.contributor.orcid0000-0003-2968-9617


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