Relevant bibliographies by topics / Jaundice, Neonatal

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Academic literature on the topic 'Jaundice, Neonatal'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Jaundice, Neonatal"

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MD, Swarnim. "Neonatal Jaundice." Journal of Medical Science And clinical Research 05, no. 05 (2017): 21519–27. http://dx.doi.org/10.18535/jmscr/v5i5.49.

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Valiyat, Shemeena, Harsha T. Valoor, Sayujya Radhamadhavan, and Salina Sasi Vayalil. "Aetiological factors and clinical profile of neonatal jaundice from a rural area of North Kerala, India." International Journal of Contemporary Pediatrics 4, no. 4 (2017): 1169. http://dx.doi.org/10.18203/2349-3291.ijcp20172023.

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Background: Neonatal jaundice is the most common problem in the first week of life leading to delayed hospital discharge and readmissions. Early recognition of neonatal hyperbilirubinemia is important to prevent serious complications. This study was done in a teaching hospital (KMCT Medical College, Mukkam, Kozhikode), in a rural area of North Kerala. It is an attempt to identify the common aetiological factors of neonatal jaundice in this setting.Methods: This observational study was conducted over a period of 6 months from January 2014 to June 2014. A total of 110 jaundiced neonates were enrolled. Data collection was done by history taking, clinical examination and relevant laboratory investigations.Results: In this study, out of 110 jaundiced neonates, 102 (92.5%) were term babies and 8 (7.3%) were preterm, 69 (62.75%) were males and 41 (37.27%) females. Physiological jaundice was seen in 44 (40%) of neonates. Various other aetiologies were ABO incompatibility 24 (21.8%), sepsis 11 (10%), Rh incompatibility 9 (8%), idiopathic 9 (8%), prematurity 8 (7.3%), cephalhematoma 7 (6.4%), breast feeding jaundice 7 (6.4%) and haemolytic anaemia 1 (0.9%).Conclusions: Physiological jaundice accounted for the bulk of cases of neonatal jaundice in our area. This was followed by ABO incompatibility. This highlights the importance of appropriate monitoring of neonates with this underlying risk factor.
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Adoba, Prince, Richard K. D. Ephraim, Kate Adomakowaah Kontor, et al. "Knowledge Level and Determinants of Neonatal Jaundice: A Cross-Sectional Study in the Effutu Municipality of Ghana." International Journal of Pediatrics 2018 (2018): 1–9. http://dx.doi.org/10.1155/2018/3901505.

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Background. Neonatal jaundice (NNJ) is a major cause of hospital admission during the neonatal period and is associated with significant mortality. This case-control study with cross-sectional design sought to identify the possible factors associated with neonatal jaundice and assess maternal knowledge level of this condition. Methods. One hundred and fifty (150) neonates comprising 100 with clinically evident jaundice and 50 without jaundice were conveniently recruited from the Trauma and Specialist Hospital in the Effutu Municipality. Blood samples were collected for the determination of serum bilirubin, glucose-6-phosphate dehydrogenase (G6PD), status and blood group (ABO and Rhesus). Well-structured questionnaire was used to collect maternal and neonate sociodemographic and clinical history. Results. Majority (54%) of neonates developed jaundice within 1–3 days after birth with 10% having it at birth. Duration of labour and neonatal birth weight were associated with neonatal jaundice (P<0.05). G6PD abnormality was found in 11 (12%) of the neonates with jaundice and ABO incompatibility was present in 18%. Neonates delivered by mothers with formal occupation and those who had prolonged duration of labour were significantly more likely to have neonatal jaundice (OR = 4.174, P=0.003; OR = 2.389, P=0.025, resp.). Neonates with low birth weight were also more likely to develop neonatal jaundice (OR = 2.347, P=0.044). Only 17.3% of mothers had heard of neonatal jaundice. School was the major source of information on neonatal jaundice (34.6%). Majority of participants (mothers) did not know that NNJ can cause damage to other organs in the body (90%). Conclusion. Low neonatal birth weight and prolonged duration of labour are associated with neonatal jaundice. Mothers had inadequate knowledge of neonatal jaundice and its causes.
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Lake, Eyasu A., Gerezgiher B. Abera, Gedion A. Azeze, Natnaeal A. Gebeyew, and Birhanu W. Demissie. "Magnitude of Neonatal Jaundice and Its Associated Factor in Neonatal Intensive Care Units of Mekelle City Public Hospitals, Northern Ethiopia." International Journal of Pediatrics 2019 (April 10, 2019): 1–9. http://dx.doi.org/10.1155/2019/1054943.

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Background. Jaundice in the neonate is one of the most common clinical problems. Globally, every year about 1.1 million babies develop it and the vast majority reside in sub-Saharan Africa and South Asia. Study on magnitude and local factors associated with neonatal jaundice is limited in Ethiopia. So this study was aimed at assessing magnitude and predictors of neonatal jaundice among neonates admitted to neonatal intensive care unit of public hospitals in Mekelle city, Northern Ethiopia. Methods. Institution based cross-sectional study was conducted from February to April 2016 in neonatal intensive care unit of Mekelle city public hospitals. Systematic random sampling technique was used to select study participants. Data was collected by interviewing mothers through structured questionnaire and reviewing neonates’ medical records using checklist. Multivariable binary logistic regression analyses were employed to identify factors associated with neonatal jaundice. Results. A total of 209 neonates with their mothers were included. The proportion of neonatal jaundice was found to be 37.3%. Prolonged labor [AOR = 4.39; 95% CI (1.8-10.69)], being male [AOR = 3.7; 95% CI (1.54-8.87)], maternal “O” blood group [AOR = 5.05; 95% CI (1.53-16.72)], sepsis [AOR = 2.64; 95% CI (1.15-6.05)], and blood type incompatibility [AOR = 18.21; 95% CI (6.36-52.13)] were positively associated with neonatal jaundice while night time delivery [AOR 0.42; 95% CI (0.18-0.96)] showed negative association. Conclusion. The magnitude of neonatal jaundice among neonates was found to be high. Duration of labor, time of delivery, sexes of neonate, sepsis, maternal blood group, and blood type incompatibility were significantly associated with neonatal jaundice. Therefore, improving newborn care and timely intervention for neonates with ABO/Rh incompatibility are recommended.
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Ali, Ambreen, Ashfaq Ahmad Shah Bukhari, Shameela Majeed, Saira Gul, Nomana Khalil, and Umair Wadood. "Frequency of Hypocalcemia with Exchange Transfusion in Neonatal Jaundice." Pakistan Journal of Medical and Health Sciences 15, no. 8 (2021): 1849–51. http://dx.doi.org/10.53350/pjmhs211581849.

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Aim: To determine the frequency of hypocalcemia with exchange transfusion in neonatal jaundice. Study design: Descriptive cross-sectional study Place and duration of study: Departments of Pediatrics and Pathology, Naseer Teaching Hospital Peshawar from 1stJanuary 2018 to 31st December 2018. Methodology: One hundred and sixty twopatients of jaundiced neonates having total serum bilirubin >20mg/dl, both gender and patients having age up to 14 days were included. Patients fulfilling the selection criteria had undergone exchange transfusion. Hypocalcaemia was evaluated and considered positive if calcium serum level is <8 mg/dl or <2 mmol/L. Results: 50% of neonates were between 1-5 days, 45% of neonates were between 5-10 days, and 3% of neonates were in age 10-14 days. One hundred and ten (68%) of neonates were males and 52 (32%) of neonates were females. 30% neonates had hypocalcemia while 70% were without hypocalcemia. Conclusion: The incidence of hypocalcemia was found to be 30% with exchange transfusion in neonatal jaundice. Keywords: Hypocalcemia, Exchange transfusion, Neonatal jaundice
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Sai Akhil, Chitturi Venkata, and Sachin Damke. "Phototherapy in Neonatal Hyperbilirubinaemia - An Overview." Journal of Evolution of Medical and Dental Sciences 10, no. 21 (2021): 1621–27. http://dx.doi.org/10.14260/jemds/2021/337.

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The first report on the use of phototherapy for treatment of neonates with jaundice was published more than 20 years ago. Since then, phototherapy has been used extensively in the treatment of neonatal hyperbilirubinaemia. Phototherapy is the use of visible light for the treatment of hyperbilirubinaemia in the newborn. There are different types of phototherapy systems in use in recent times. Effectiveness of phototherapy depends on several factors which should be considered while delivering phototherapy to a jaundiced neonate. Effective phototherapy has decreased the need for exchange transfusion. Proper nursing care enhances the effectiveness of phototherapy and minimises complications. Jaundice is benign in most of the cases, but because of potential bilirubin toxicity, strict and close monitoring is required. Prompt recognition and intervention of the infants at increased risk for developing hyperbilirubinaemia forms the first step in management. The focus is to prevent development of severe hyperbilirubinaemia by early recognition and initiation of treatment. Counselling of parents, especially mother also plays a major role in the treatment of neonatal jaundice. Recommended guidelines are intended to be used by hospitals and treating paediatricians, neonatologists and advanced practice nurses trained in neonatology. Phototherapy devices include fluorescent, halogen, fibreoptic or light emitting diode light sources. Each type has its own benefits and side effects. Many studies were available comparing the efficacy of various types of phototherapy systems. The purpose of this review article was to provide a conceptual review on role of phototherapy in neonatal jaundice, different types of phototherapy systems in use, recent advances and probable side effects of phototherapy. KEY WORDS Bilirubin, Hyperbilirubinaemia, Jaundice, Neonatal Intensive Care, Newborn, Phototherapy
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Acharya, Niraj, and Chandra Prasad Paneru. "Prevalence and Etiology of Neonatal Jaundice in a Tertiary Care Hospital." Journal of Nepalgunj Medical College 18, no. 2 (2021): 35–38. http://dx.doi.org/10.3126/jngmc.v18i2.38891.

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Introduction: Neonatal jaundice is a major clinical condition worldwide occurring in upto 60% of term and 80% preterm newborn in the first week of life. Neonatal jaundice is defined as total serum bilirubin level above 7 mg/dl.
 Aims: This study was done to find out the prevalence and etiology of neonatal jaundice in neonates admitted to Neonatal Intensive Care Unit (NICU) of Nepalgunj Medical College Teaching Hospital (NGMCTH) Kohalpur, Banke.
 Methods: It was a prospective cross sectional hospital based study conducted from November 2018 to November 2019 in Neonatal Intensive Care Unit of Nepalgunj Medical College Teaching Hospital. All neonates with clinical jaundice and hyperbilirubinemia with total serum bilirubin of ≥7 mg/dl were subjected to complete history taking, through physical examination and investigations.
 Results: Out of 892 neonates who developed clinical jaundice, 640 neonates whose parents gave consent were included in the study. The prevalence of neonatal jaundice was found to be 39.85% with male to female ratio of 1.79:1. In the present study pathological jaundice was seen in 74.94% whereas physiological jaundice in 23.66%. Among the various etiologies of pathological jaundice, neonatal sepsis (44.52%) was found to be the most common cause followed by ABO incompatibility (12.18%) and Rh incompatibility (7.03%).
 Conclusion: The prevalence of neonatal jaundice in present study was 39.85% and the most common cause was neonatal sepsis .The prevalence of jaundice was more in preterm than in term neonates. Neonatal jaundice is very common morbidity in NICU especially in preterm babies.
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Demet Cabar, Huriye, Adeviye Aydin, and Ulgen Gullu. "Care in neonatal jaundice." International Journal of Academic Research 6, no. 3 (2014): 8–14. http://dx.doi.org/10.7813/2075-4124.2014/6-3/a.2.

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Althomali, Ruya, Renad Aloqayli, Basma Alyafi, et al. "Neonatal jaundice causes and management." International Journal Of Community Medicine And Public Health 5, no. 11 (2018): 4992. http://dx.doi.org/10.18203/2394-6040.ijcmph20184604.

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80% of healthy neonates present with some degree of hyperbilirubinemia after birth, however, only 5-10% would require therapy to prevent damage or treat the cause of jaundice. Neonatal jaundice can be classified as physiological and pathological and can have several causes such as breast milk feeding, blood group incompatibility, hemolysis, or genetic defects of enzymes in the bilirubin metabolism pathway. We tried to understand the various types of neonatal jaundice, and also focus on its management. We conducted this review using a comprehensive search of MEDLINE, PubMed and EMBASE from January 2001 to March 2017. The following search terms were used: neonatal jaundice, hyperbilirubinemia, ABO incompatibility, neonatal hemolysis, kernicterus, phototherapy, exchange transfusion. Hyperbilirubinemia and jaundice are common issues encountered neonates and infants. Most cases of neonatal hyperbilirubinemia and jaundice are physiological and benign. However, some severe cases may progress to develop severe and permanent long-term complications. Therefore, early diagnosis and management is essential. Neonatal jaundice can be treated using phototherapy, pharmacological agents, intravenous immunoglobulins and exchange transfusion in severe cases.
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Melton, Kristin, and Henry T. Akinbi. "Neonatal jaundice." Postgraduate Medicine 106, no. 6 (1999): 167–78. http://dx.doi.org/10.3810/pgm.1999.11.775.

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Dissertations / Theses on the topic "Jaundice, Neonatal"

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Greville, K. A. "Central auditory processing in children with a history of neonatal jaundice." Thesis, University of Auckland, 1990. http://hdl.handle.net/2292/1986.

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An experimental group (Group A) of 22 children around 7 years of age who had normal hearing for pure tones but who had experienced neonatal jaundice with peak bilirubin levels of at least 300 µmol/l was tested on a range of audiological tests selected to assess aspects of their central auditory processing. Children who had not been tested for bilirubin level were selected as control subjects (Group B); they were matched on the variables gender, race, gestational age, birthweight, Apgar scores and occurrence of respiratory problems. A smaller experimental group, Group C (n=7), with peak bilirubin levels between 250 and 299 µmol/l but with perinatal complications was also studied. The experimental groups had higher mean acoustic reflex thresholds and lower mean reflex amplitudes than the control group. Acoustic reflex threshold patterns of abnormality consistent with central dysfunction occurred in two children from the main experimental group and two children in the control group. None of the children from Group C showed abnormal reflex thresholds. Acoustic reflex amplitude patterns of abnormality consistent with central dysfunction were present in six children from Group A and two children from Group C, compared with three children from the control group. Masking level differences were absent in five subjects from Group A and three children from Group C, compared with three control subjects. No group differences were evident for ABR latency or amplitude measures, but poor morphology or repeatability of wave V was observed in ten subjects from Group A and three children from Group C, compared with five children from the control group. A larger number of failures within the experimental groups was found for two of the four speech tests, that is, for interrupted and filtered speech tests, but not speech in noise or competing words tests. Five children from Group A (but none from Group C) performed poorly on the interrupted speech test, compared with two from Group B. The filtered speech test was failed by six children from Group A and two children from Group C, compared with two from Group B. Parental reports of behavioural or learning disorders were distributed equally among the groups and were not associated with particular patterns of test failure. Overall, children in the experimental groups failed significantly more tests of central auditory functioning than did children in the control group (F(2,48)=5.5,p<.01). The results were interpreted as implicating jaundice in long-term central auditory processing abnormalities.
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倪建春 and Kin-chun Ngai. "Demonstration of bilirubin cytotoxicity by tissue culture system." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1996. http://hub.hku.hk/bib/B31214526.

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Ngai, Kin-chun. "Demonstration of bilirubin cytotoxicity by tissue culture system /." Hong Kong : University of Hong Kong, 1996. http://sunzi.lib.hku.hk/hkuto/record.jsp?B18155030.

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Annandale, Elizabeth. "Die etiologiese verband tussen verstadigde neurologiese integrasie en latere leerproblematiek by kinders met klinies betekenisvolle neonatale bilirubienmetings." Pretoria : [s.n.], 2008. http://upetd.up.ac.za/thesis/available/etd-09252008-122227/.

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Matsumoto, Maya. "Improving the Timing of Bilirubin Screening in the Neonatal Intensive Care Unit." Scholarship @ Claremont, 2018. http://scholarship.claremont.edu/cmc_theses/1976.

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Background Hyperbilirubinemia is a condition that affects most infants, but typically self-resolves and is not harmful. However, if bilirubin levels exceed neuroprotective defenses, the compound can cross the blood-brain barrier and have neurotoxic and potentially fatal effects. Treatment of neonatal hyperbilirubinemia with phototherapy is necessary for the prevention of kernicterus. Guidelines for the use of phototherapy in infants born at ≥ 35 weeks’ gestation were published by Bhutani et al. and endorsed by the American Academy of Pediatrics. Consensus-based recommendations for phototherapy treatment and exchange transfusion of premature infants were published in 2012 by Maisels, et al. However, there are no published recommendations for the timing of screening for hyperbilirubinemia in NICU patients. In 2012, the Kapʻiolani Medical Center for Women & Children Neonatology Division implemented internal guidelines for phototherapy with recommendations for the timing of screening serum bilirubin levels, based on the group’s opinion. Five years later, the current study queried whether these guidelines for screening were appropriate. Objective The present study sought to describe current practices of obtaining serum bilirubin levels and the use of phototherapy in the NICU during the first five days of life. It was hypothesized that many bilirubin levels obtained at ≤ 48 hours of life are below published recommended treatment thresholds and are potentially unnecessary. Methods Retrospective chart review was performed on all infants admitted to the NICU at < 24 hours of life, from July 2016-June 2017. Eligible infants were divided into three gestation age groups: ≤ 28, 29-35, and ≥ 36 weeks at birth. Patient demographics, bilirubin levels, and phototherapy treatment were noted. The primary outcome of interest was the percent of serum bilirubin levels obtained during the first 48 hours of life that did not meet phototherapy treatment criteria. Results 931 charts were reviewed. Infants born at ≤ 28, 29-35 and ≥ 36 weeks’ gestation made up 10%, 51% and 39% of the cohort. Overall mortality was 3%, and no exchange transfusions were performed during the study period. At least one serum bilirubin level was obtained for 96% of the patients, but only 55% were treated with phototherapy within the first five days of life. Phototherapy was rarely prescribed on day of life (DOL) 1 (0.7%). By DOL 2, a total of 563 bilirubin levels were obtained, but only 108 infants (19%) were treated with phototherapy. However, one-third of these patients’ bilirubin levels did not meet published criteria for treatment. The timing of phototherapy treatment varied by gestational age. Ninety percent of infants born ≤ 28 weeks’ gestation who received phototherapy were treated starting between DOL 2-3. In contrast, eighty-five percent of infants born ≥ 29 weeks’ gestation who received phototherapy, started on DOL 3-5. Discussion Far more bilirubin levels were obtained than courses of phototherapy prescribed. Given the distinct patterns of phototherapy for infants of varying gestational age, there is ample opportunity to improve resource utilization with targeted recommendations for obtaining screening bilirubin levels in the neonate without early jaundice.
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Chen, Wenxiong. "Neonatal hyperbilirubinemia long-term neurophysiological and neurodevelopmental outcomes /." Click to view the E-thesis via HKUTO, 2006. http://sunzi.lib.hku.hk/hkuto/record/B37489380.

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Chen, Wenxiong, and 陈文雄. "Neonatal hyperbilirubinemia: long-term neurophysiological and neurodevelopmental outcomes." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2006. http://hub.hku.hk/bib/B37489380.

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CALY, JOSE P. "Estudo e avaliacao da radiometria no tratamento fototerapico da hiperbilirrubinemia neonatal." reponame:Repositório Institucional do IPEN, 2009. http://repositorio.ipen.br:8080/xmlui/handle/123456789/9395.

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Made available in DSpace on 2014-10-09T12:26:28Z (GMT). No. of bitstreams: 0<br>Made available in DSpace on 2014-10-09T14:09:41Z (GMT). No. of bitstreams: 0<br>Tese (Doutoramento)<br>IPEN/T<br>Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP
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Carvalho, Clarissa Gutierrez. "Polimorfismos genéticos em neonatos hiperbilirrubinêmicos com mais de 35 semanas de idade gestacional." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2009. http://hdl.handle.net/10183/16562.

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A icterícia neonatal é geralmente benigna, mas desfechos desfavoráveis podem ocorrer e a identificação dos casos de maior risco seria muito útil. Alguns fatores de risco já conhecidos são prematuridade, desidratação, aleitamento materno, deficiência de G6PD e incompatibilidade sanguínea. As alterações na conjugação hepática de bilirrubina devido a polimorfismos da UGT1A1 também podem contribuir para esse maior risco. O objetivo deste estudo foi estimar a freqüência da deficiência de G6PD e/ou das variantes polimórficas da UGT1A1 como fatores de risco para hiperbilirrubinemia grave em neonatos com mais de 35 semanas de idade gestacional e peso superior a 2000g em uma Unidade Neonatal do Sul do Brasil. Estudo prospectivo, observacional, de casos e controles, que incluiu 243 recémnascidos admitidos para fototerapia no HCPA e 247 controles, entre março e dezembro de 2007. Foi realizada dosagem da atividade da G6PD e análises genético-moleculares do respectivo gene. Foi também realizado PCR para a UGT1A1 com eletroforese capilar em analisador genético ABI 3130xl e análise no programa GeneMapper®. Foram detectados genótipos polimórficos da UGT1A1 em 16% dos pacientes, com prevalência nos ictéricos de 13,5% e nos normais de 18,2%, diferença não significativa. Identificada maior prevalência dos polimorfismos em negros e pardos (25%) em relação aos brancos (13%) (p=0,014). A prevalência da deficiência de G6PD foi 4,6%, sem mostrar correlação com a icterícia. Concluímos que nesta amostra de recém-nascidos do sul do Brasil nem as variantes da UGT1A1, nem a deficiência de G6PD foram associadas à hiperbilirrubinemia grave, com prevalências semelhantes às verificadas em outras populações. Considerando a grande miscigenação presente nessa região, outros fatores e interações gênicas devem ser procurados, incluindo possivelmente o estudo de outros polimorfismos, identificando fatores de risco para explicar a doença, um importante problema de saúde a merecer a atenção dos pesquisadores.<br>Neonatal jaundice is usually benign, but unfavorable outcomes may happen; therefore, the identification of high-risk cases would be very useful. Some risk factors already known are prematurity, dehydration, breastfeeding, G6PD deficiency and blood incompatibility. Alterations in the hepatic conjugation of bilirubin due to UGT1A1 polymorphisms may also contribute to this higher risk. The objective of this study was to estimate the frequency of G6PD deficiency and the promoter region of UGT1A1 gene variants as risk factors to severe hyperbilirubinemia in newborns of over 35 weeks of gestational age and weighing above 2,000g in a Neonatal Service in Southern Brazil. This is a prospective and observational study of cases and controls which included 243 newborns admitted for phototherapy at HCPA and 247 controls, between March and December, 2007. G6PD activity was determined and the deficient cases were investigated by genetic analysis. PCR for the UGT1A1 variants was also performed, followed by capillary electrophoresis in genetic analyzer ABI 3130xl and the analysis in GeneMapper® program. Polymorphic genotypes were detected in 16% of the patients, prevalence in icteric patients was 13,5% and in normal individuals was 18,2%, a difference which was not significant. A higher prevalence of polymorphisms in blacks and mulattos (25%) was identified when compared to whites (13%) (p=0,014). A prevalence of 4,6% of G6PD deficiency was found, without association to jaundice. We concluded that in this sample of newborns from the South of Brazil, polymorphic variants of UGT1A1 were not associated to severe hyperbilirubinemia as well as G6PD deficiency; being the prevalence similar to those found in other populations. Considering the high miscegenation that occurs in this area of Brazil, perhaps other factors and genic interactions should be sought in order to identify genetic risk factors, possibly including the study of further polymorphisms, as neonatal jaundice remains an important health problem to be approached by investigators.
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Zietz, Burkhard. "An Ultrafast Spectroscopic and Quantum-Chemical Study of the Photochemistry of Bilirubin : Initial Processes in the Phototherapy for Neonatal Jaundice." Doctoral thesis, Umeå : Dept. of Chemistry, Umeå University, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-672.

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Books on the topic "Jaundice, Neonatal"

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Care of the jaundiced neonate. McGraw-Hill Medical, 2012.

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Jährig, Klaus. Phototherapy: Treating neonatal jaundice with visible light. Quintessenz, 1993.

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Maines, Mahin D. Heme oxygenase: Clinical applications and functions. CRC Press, 1992.

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Lee, Kyong-Soon. An evaluation of the rate and the severity of readmissions for jaundice or dehydration associated with shorter neonatal hospital stay. National Library of Canada, 1995.

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Stamatas, Georgios N. Photobiology of infant skin. Nova Science, 2010.

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Stamatas, Georgios N. Photobiology of infant skin. Nova Biomedical Press, 2010.

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Beattie, R. Mark, Anil Dhawan, and John W.L. Puntis. Neonatal jaundice. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569862.003.0047.

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Epidemiology 340Unconjugated hyperbilirubinaemia 340Specific conditions 342Conjugated hyperbilirubinaemia 343Idiopathic neonatal hepatitis 347• 30–50% of normal term newborns are jaundiced after birth.• Physiological and breast milk jaundice account for the majority of cases.• 1 in 2500 infants has conjugated hyperbilirubinaemia....
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Kyrana, Eirini, and Nancy Tan. Neonatal jaundice. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198759928.003.0053.

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The chapter on neonatal jaundice covers the pathophysiology of jaundice with an extensive differential for unconjugated and conjugated jaundice. It includes suggested investigations and management, as well as more detailed information on idiopathic neonatal hepatitis.
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Rubaltelli, Firmino. Neonatal Jaundice. Springer, 2013.

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Wilson, Deborah Low. Axillary and rectal temperatures in healthy neonates with physiologic jaundice receiving phototherapy. 1988.

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Book chapters on the topic "Jaundice, Neonatal"

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Medway, Frederic J., and Suzanne Thomas. "Jaundice (neonatal)." In Health-related disorders in children and adolescents: A guidebook for understanding and educating. American Psychological Association, 1998. http://dx.doi.org/10.1037/10300-049.

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Bartels, Iris, Frank Beier, Peter L. M. Jansen, et al. "Jaundice, Neonatal." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_1251.

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Froehlich, Stephan J., Carlo A. Lackerbauer, Guenter Rudolph, et al. "Neonatal Jaundice." In Encyclopedia of Molecular Mechanisms of Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_9285.

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Justinich, Christopher J., and Jeffrey S. Hyams. "Neonatal Jaundice." In Diseases of the Liver and Bile Ducts. Humana Press, 1998. http://dx.doi.org/10.1007/978-1-4612-1808-1_22.

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Petty, Julia. "Jaundice." In Bedside Guide for Neonatal Care. Macmillan Education UK, 2015. http://dx.doi.org/10.1007/978-1-137-39847-5_12.

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Kianiamin, Mojgan, and Nima Rezaei. "Neonatal Jaundice and Leukopenia." In Pediatric Immunology. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-21262-9_31.

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Crawford, Doreen. "Nursing care of a baby with jaundice." In Neonatal Nursing. Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3101-6_13.

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Ennever, John F. "Light Therapy for Neonatal Jaundice." In Optronic Techniques in Diagnostic and Therapeutic Medicine. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3766-3_14.

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Bielza, Concha, Sixto Ríos-Insua, and Manuel Gómez. "Influence Diagrams for Neonatal Jaundice Management." In Artificial Intelligence in Medicine. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/3-540-48720-4_13.

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Banu, P. K. Nizar, Hala S. Own, Teodora Olariu, and Iustin Olariu. "Cluster Analysis for European Neonatal Jaundice." In Soft Computing Applications. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-62521-8_35.

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Conference papers on the topic "Jaundice, Neonatal"

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Mazur, Olena, Olga Yablon, Tatiana Savrun, Anastasiia Konoplitska, and Nataliia Chornopyshchuk. "Diagnostic Markers of Prolonged Neonatal Jaundice." In 9th ICCN International Conference on Clinical Neonatology—Selected Abstracts. Thieme Medical Publishers, 2020. http://dx.doi.org/10.1055/s-0040-1716972.

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Hamza, Mostafa, and Mohammad Hamza. "Laser Photoradiation Therapy For Neonatal Jaundice." In OE LASE'87 and EO Imaging Symp (January 1987, Los Angeles), edited by Lee R. Carlson. SPIE, 1987. http://dx.doi.org/10.1117/12.939674.

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Yasmeen, Tayyaba, William McCue, Veronica McArthur, and Allan Jackson. "GP250 NEONATAL JAUNDICE SURVEILLANCE- ARE WE WINNING?" In Faculty of Paediatrics of the Royal College of Physicians of Ireland, 9th Europaediatrics Congress, 13–15 June, Dublin, Ireland 2019. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2019. http://dx.doi.org/10.1136/archdischild-2019-epa.309.

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Outlaw, Felix, Judith Meek, Lindsay W. MacDonald, and Terence S. Leung. "Screening for Neonatal Jaundice with a Smartphone." In DH '17: International Conference on Digital Health. ACM, 2017. http://dx.doi.org/10.1145/3079452.3079488.

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Agati, Giovanni, Franco Fusi, Riccardo Pratesi, Simone Pratesi, and Gian Paolo Donzelli. "Colorful story of phototherapy for neonatal jaundice." In BiOS Europe '96, edited by Stanley B. Brown, Benjamin Ehrenberg, and Johan Moan. SPIE, 1996. http://dx.doi.org/10.1117/12.260751.

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Hunt, Laura, Marie Ramos, Yvonne Helland, and Karen Lamkin. "19 Decreasing neonatal jaundice readmission rates through implementation of a jaundice management guide." In IHI Scientific Symposium. British Medical Journal Publishing Group, 2020. http://dx.doi.org/10.1136/bmjoq-2020-ihi.19.

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Yang, Chun, Haihong Hu, Zheng Yang, Jinhui Hu, and Hong Mo. "Application of Fuzzy Sets in Neonatal Pathological Jaundice." In 2020 7th International Conference on Information, Cybernetics, and Computational Social Systems (ICCSS). IEEE, 2020. http://dx.doi.org/10.1109/iccss52145.2020.9336930.

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Sohani, Mohammad, Behrooz Makki, Nasser Sadati, Kamran Kahosrovian Kermani, and Ali Riazati. "A Neuro-Fuzzy Approach to Diagnosis of Neonatal Jaundice." In 2006 1st Bio-Inspired Models of Network, Information and Computing Systems. IEEE, 2006. http://dx.doi.org/10.1109/bimnics.2006.361808.

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Sohani, Mohammad, Kamran Khosrovian Kermani, Behrooz Makki, Ali Riazati, and Nasser Sadati. "A Neuro-Fuzzy Approach to Diagnosis of Neonatal Jaundice." In 2006 1st Bio-Inspired Models of Network, Information and Computing Systems. IEEE, 2006. http://dx.doi.org/10.1109/bimnics.2006.361809.

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Sohani, Mohammad, Kamran Khosrovian Kermani, Behrooz Makki, Ali Riazati, and Nasser Sadati. "A Neuro-Fuzzy approach to diagnosis of neonatal jaundice." In the 1st international conference. ACM Press, 2006. http://dx.doi.org/10.1145/1315843.1315863.

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Reports on the topic "Jaundice, Neonatal"

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Gao, Yang, Xiangbin Kong, and Jiajun Xiang. Ursodeoxycholic acid in the treatment of neonatal jaundice: a systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2021. http://dx.doi.org/10.37766/inplasy2021.2.0027.

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