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Books on the topic 'Neonatal adverse effects'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Seto, Arnold Henning. Meta-analysis of adverse neonatal effects due to maternal exposure to antihistamines. National Library of Canada, 1994.

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2

Lee, Wetherington Cora, Smeriglio Vincent L, Finnegan Loretta P, and National Institute on Drug Abuse., eds. Behavioral studies of drug-exposed offspring: Methodological issues in human and animal research. U.S. Dept. of Health and Human Services, National Institutes of Health, National Institute on Drug Abuse, 1996.

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3

Briggs, Gerald G. Drugs in pregnancy and lactation: A reference guide to fetal and neonatal risk. 3rd ed. Williams & Wilkins, 1990.

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4

1935-, Freeman Roger K., and Yaffe Sumner J. 1923-2011, eds. Drugs in pregnancy and lactation: A reference guide to fetal and neonatal risk. 3rd ed. Williams & Wilkins, 1990.

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5

1935-, Freeman Roger K., and Yaffe Sumner J. 1923-, eds. Drugs in pregnancy and lactation: A reference guide to fetal and neonatal risk. 6th ed. Lippincott Williams & Wilkins, 2002.

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6

Briggs, Gerald G. Drugs in pregnancy and lactation: A reference guide to fetal and neonatal risk on CD-ROM. Lippincott, Williams & Wilkins, 1999.

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7

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

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8

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

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9

1927-, Poswillo David E., Alberman Eva D, and Great Britain. Dept. of Health., eds. Effects of smoking on the fetus, neonate, and child. Oxford University Press, 1992.

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10

Seto, Arnold Henning. Meta-analysis of adverse neonatal effects due to maternal exposure to antihistamines. 1993.

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11

Drugs in Pregnancy and Lactation: A Reference Guide to Fetal and Neonatal Risk. Williams & Wilkins, 1986.

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12

Drugs in Pregnancy and Lactation: A Reference Guide to Fetal and Neonatal Risk (Drugs in Pregnancy and Lactation). 8th ed. Lippincott Williams & Wilkins, 2008.

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13

Briggs, Gerald G., R. K. Freeman, and S. J. Yaffe. Drugs in Pregnancy and Lactation: A Reference Guide to Fetal and Neonatal Risk. Lippincott Williams & Wilkins,US, 1999.

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14

Drugs in Pregnancy and Lactation: A Reference Guide to Fetal and Neonatal Risk. 7th ed. Lippincott Williams & Wilkins, 2005.

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15

Drugs in Pregnancy & Lactation: A Reference Guide to Fetal & Neonatal Risk. 5th ed. Williams & Wilkins, 1998.

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16

Drugs in Pregnancy and Lactation: A Reference Guide to Fetal and Neonatal Risk. LWW, 2014.

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17

Voinescu, P. Emanuela. A 27-Year-Old Woman with Epilepsy Planning for Pregnancy. Edited by Angela O’Neal. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190609917.003.0028.

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Treatment for women with epilepsy (WWE) of childbearing age should be cautiously selected, given that the benefits of treatment during potential future pregnancies have to be weighed against the adverse effects on the developing fetus. The number of antiepileptic drugs (AEDs) has increased significantly in the last 20 years, and remarkable progress has been made in characterizing their teratogenicity, adverse neonatal outcomes, and neurodevelopmental problems. Not only the AED choice, but the number of AEDs used and their dose are also important. This chapter aims to introduce some of the basi

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18

Balzafiore, Danielle, Thalia Robakis, Sarah Borish, Vena Budhan, and Natalie Rasgon. The treatment of bipolar disorder in women. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198748625.003.0020.

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Sex-specific effects in the clinical presentation and course of bipolar disorder in women have important treatment implications for the management of symptoms across the menstrual cycle and reproductive lifespan. Women with bipolar disorder are particularly vulnerable to premenstrual mood symptoms, menstrual abnormalities, and polycystic ovary syndrome. Special considerations include understanding the interactions between these reproductive issues, oral contraceptives, and mood-stabilizing agents. Additionally, the management of bipolar disorder during the perinatal period requires a careful a

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19

Lynch, Tara A., and J. Christopher Glantz. Seizure Medications Effects on Fetus, Neonate, and Lactation. Edited by Emma Ciafaloni, Cheryl Bushnell, and Loralei L. Thornburg. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190667351.003.0021.

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Medication use in pregnancy requires a careful balance between the risks of fetal teratogenicity and the maternal benefits of disease treatment. For women with epilepsy, there are many antiepileptic medications available for use in pregnancy. Each varies in their safety profile, risk for fetal anomalies, and effectiveness of seizure control. In most scenarios, the benefits of maternal treatment outweigh the risk of fetal effects, especially in cases of refractory epilepsy or severe disease. Many of the newer anti-epileptic drugs appear to have less teratogenic risk than the older medications.

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20

Fichtner, Alexander, and Franz Schaefer. Acute kidney injury in children. Edited by Norbert Lameire. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0239.

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In the past few decades, the overall incidence of acute kidney injury (AKI) in paediatric patients has increased and the aetiological spectrum has shifted from infection-related and intrinsic renal causes towards secondary forms of AKI related to exposure to nephrotoxic drugs and complex surgical, oncological, and intensive care manoeuvres. In addition, neonatal kidney impairment and haemolytic uraemic syndrome continue to be important specific paediatric causes of AKI raising unique challenges regarding prevention, diagnosis, and treatment. The search for new biomarkers is a current focus of

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21

(US), National Research Council. Evaluating Chemical and Other Agent Exposures For Reproductive and Developmental Toxicity. National Academies Press, 2001.

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22

Jacquemyn, Yves, and Anneke Kwee. Antenatal and intrapartum fetal evaluation. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198713333.003.0006.

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Antenatal and intrapartum fetal monitoring aim to identify the beginning of the process of fetal hypoxia before irreversible fetal damage has taken place. Fetal movement counting by the mother has not been reported to be of any benefit. The biophysical profile score, incorporating ultrasound and fetal heart rate monitoring, has not been proven to reduce perinatal mortality in randomized trials. Doppler ultrasound allows the exploration of the perfusion of different fetal organ systems and provides data on possible hypoxia and fetal anaemia. Maternal uterine artery Doppler can be used to select

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