Neurobehavior of Full-Term Small for Gestational Age Newborn Infants Of

Total Page:16

File Type:pdf, Size:1020Kb

Neurobehavior of Full-Term Small for Gestational Age Newborn Infants Of 0021-7557/08/84-03/217 Jornal de Pediatria Copyright © 2008 by Sociedade Brasileira de Pediatria ARTIGO ORIGINAL Neurobehavior of full-term small for gestational age newborn infants of adolescent mothers Neurocomportamento de recém-nascidos a termo, pequenos para a idade gestacional, filhos de mães adolescentes Marina C. de Moraes Barros1, Ruth Guinsburg2, Sandro S. Mitsuhiro3, Elisa Chalem4, Ronaldo R. Laranjeira5 Resumo Abstract Objetivo: Comparar o neurocomportamento de recém-nascidos Objective: To compare the neurobehavior of small (SGA) and a termo pequenos (PIG) e adequados (AIG) para a idade gestacional, adequate (AGA) for gestational age full-term neonates born to filhos de mães adolescentes. adolescent mothers. Métodos: Estudo transversal prospectivo de nascidos a termo Methods: This prospective cross-sectional study included AIG e PIG, com 24-72 horas de vida, sem afecções do sistema nervoso full-term newborn infants aged 24-72 hours, free from central central. Os neonatos foram avaliados por meio da Neonatal Intensive nervous system malformations and born to adolescent mothers at a Care Unit Network Neurobehavioral Scale (NNNS) para: habituação, single center in Brazil. Infants were assessed with the Neonatal atenção, despertar,controle, manobras para a orientação, qualidade Intensive Care Unit Network Neurobehavioral Scale (NNNS) for: dos movimentos, excitabilidade, letargia, reflexos não ótimos, habituation, attention, arousal, regulation, handling, quality of assimetria, hipertonia, hipotonia e sinais de estresse e abstinência. movement, excitability, lethargy, nonoptimal reflexes, asymmetry, A comparação dos grupos AIG e PIG foi feita por análise de variância hypertonia, hypotonia, and stress/abstinence signals. The chi-square e teste do qui-quadrado. Aplicou-se a regressão multivariada para test and analysis of variance were used to compare SGA and AGA analisar os fatores associados ao escore de cada variável do NNNS. infants. Multivariate regression was used to analyze factors Resultados: Dos 3.685 nascidos no local do estudo, 928 (25%) associated with the score of each NNNS variable. eram de mães adolescentes. Desses, 477 satisfizeram os critérios Results: Of 3,685 infants born in the study hospital, 928 (25%) de inclusão, sendo 419 (88%) AIG e 58 (12%) PIG. A análise had adolescent mothers. Of these, 477 infants met the inclusion univariada não mostrou diferença em nenhuma das variáveis da criteria: 419 (88%) were AGA and 58 (12%) were SGA. Univariate NNNS entre os PIG e os AIG. Na análise multivariada, os PIG nascidos analysis did not show any differences between AGA and SGA neonates de parto vaginal apresentaram menor escore na variável qualidade in terms of NNNS variables. Multivariate analysis showed that SGA de movimentos do que os nascidos por cesárea. Os PIG nascidos com neonates born by vaginal delivery had lower scores for quality of anestesia local ou sem anestesia apresentaram maior escore na movements than those born by caesarean section. The SGA neonates variável excitabilidade do que os nascidos sob anestesia born with local or without anesthesia had higher scores for excitability loco-regional. Os PIG femininos tiveram menor escore na variável than those born with spinal anesthesia. Additionally, female SGA sinais de estresse/abstinência que os masculinos. neonates had lower scores for stress/abstinence signals than males. Conclusão: Os recém-nascidos PIG de mães adolescentes Conclusion: SGA neonates born to adolescent mothers showed mostraram menor qualidade de movimento, mais excitabilidade e poorer quality of movements, more excitability and more signals of mais sinais de estresse, em associação com o sexo do neonato e com stress in association with sex of infant and variables related to variáveis relacionadas ao parto. delivery. J Pediatr (Rio J). 2008;84(3):217-223: Comportamento, gravidez J Pediatr (Rio J). 2008;84(3):217-223: Behavior, pregnancy in na adolescência, recém-nascido. adolescence, infant, newborn. 1. Doutora, Universidade Federal de São Paulo - Escola Paulista de Medicina (UNIFESP-EPM), São Paulo, SP. 2. Professora titular, Departamento de Pediatria, UNIFESP-EPM, São Paulo, SP. 3. Doutor, UNIFESP-EPM, São Paulo, SP. 4. Psicóloga pesquisadora, Unidade de Pesquisa em Álcool e Drogas, UNIFESP-EPM, São Paulo, SP. 5. Professor livre-docente, Departamento de Psiquiatria, UNIFESP-EPM, São Paulo, SP.Chefe, Unidade de Pesquisa em Álcool e Drogas, UNIFESP-EPM, São Paulo, SP. Apoio financeiro: FAPESP, projeto nº 00/10.293-5. Não foram declarados conflitos de interesse associados à publicação deste artigo. Como citar este artigo: Barros MC, Guinsburg R, Mitsuhiro SS, Chalem E, Laranjeira RR. Neurobehavior of full-term small for gestational age newborn infants of adolescent mothers. J Pediatr (Rio J). 2008;84(3):217-223. Artigo submetido em 13.12.07, aceito em 27.02.08. doi:10.2223/JPED.1796 217 218 Jornal de Pediatria - Vol. 84, Nº 3, 2008 Neurocomportamento de recém-nascidos PIG - Barros MC et al. Introdução O neurocomportamento, em recém-nascidos PIG, além de pouco estudado, não conta com homogeneidade em relação O recém-nascido pequeno para a idade gestacional (PIG) à definição de “pequeno para a idade gestacional” nem quanto resulta da restrição de crescimento intra-uterino, que pode ao método de avaliação neurocomportamental. Neste con- ser desencadeada por uma série de fatores inerentes à saúde texto, o presente estudo tem por objetivo comparar o perfil da mãe e do feto, além daqueles relacionados à situação socio- neurocomportamental de recém-nascidos a termo, filhos de econômica da família. A gravidez na adolescência, a ausência mães adolescentes, PIG e AIG, por meio da Neonatal Inten- de parceiro fixo, a baixa escolaridade, a realização inade- sive Care Unit Neurobehavioral Network Scale (NNNS). quada de pré-natal, o uso de drogas lícitas e ilícitas, a expo- sição a doenças sexualmente transmissíveis, à violência e a Métodos distúrbios psicopatológicos podem, de maneira conjunta ou Trata-se de estudo de transversal, unicêntrico, com coleta isolada, levar ao crescimento inadequado do feto1,2.Noque prospectiva de dados, em um hospital de nível terciário do se refere à gestação na adolescência, esta se acompanha com município de São Paulo (SP), no período de julho de 2001 a certa freqüência de exposição à violência e à presença de novembro de 2002. O estudo foi aprovado pelo Comitê de desordens mentais, sendo a violência durante a gravidez ado- Ética em Pesquisa do hospital onde foi realizada a coleta de lescente associada ao nascimento de PIG, ao passo que as dados e da instituição de ensino dos pesquisadores, sendo doenças mentais se associam à prematuridade3. Por outro financiado pela Fundação de Apoio à Pesquisa do Estado de lado, a gravidez na adolescência não representa fator de risco São Paulo. para baixo peso ao nascer quando a influência de fatores clí- nicos, gestacionais e psicossociais desfavoráveis é afastada4. Para a constituição da casuística, foram considerados os seguintes critérios de inclusão: assinatura do termo de con- Sabe-se que a desnutrição intra-uterina influencia a matu- sentimento livre esclarecido materno, recém-nascido filho de ração anatômica e funcional do sistema nervoso central. A mãe adolescente (idade 10-19 anos), a termo (idade gesta- insuficiência placentária crônica, que resulta em restrição do cional 37-416,7 semanas), sendo a idade gestacional calcu- crescimento fetal, leva a déficits de conexão neural e mielini- lada a partir da data da última menstruação ou, quando este zação e altera a funcionalidade dos sistemas auditivo e visual dado não estava disponível, estimada pelo método de New 5 no período pós-natal . No recém-nascido a termo PIG, estu- Ballard17. dos volumétricos por ressonância magnética indicam redu- ção da substância cinzenta, sendo o hipocampo especialmente Foram excluídos os neonatos que apresentaram uma ou vulnerável aos efeitos da insuficiência placentária6. Além mais das seguintes condições que poderiam interferir nas res- disso, em fetos com restrição grave do crescimento intra- postas neurocomportamentais: mães com sorologia positiva uterino, há comprometimento do crescimento cortical, com na gestação ou parto para infecções congênitas; mães que diminuição do número de células no córtex cerebral7. Tais receberam opióides, sedativos e/ou anticonvulsivantes nas modificações do crescimento e desenvolvimento do sistema 24 horas antes do parto ou anestesia geral para o parto; nervoso central podem desencadear alterações neurocom- recém-nascidos expostos intra-útero ao tabaco, álcool, maco- portamentais perceptíveis já nos primeiros dias de vida8. nha, cocaína ou outra droga; gemelares; pacientes com bole- tim de Apgar<3no1ºminuto ou<7no5ºminuto de vida; A descrição clássica do recém-nascido PIG inclui maior recém-nascidos com malformações congênitas maiores; e habilidade motora, resposta exacerbada à pesquisa dos refle- presença de intercorrências clínicas no dia do estudo. Foram xos, permanência prolongada em estado de alerta e mais ape- incluídos os neonatos ictéricos que não estavam em fototera- tite do que neonatos de mesmo peso, porém menor idade pia à época do exame e aqueles que haviam apresentado des- gestacional9. No entanto, estudos de aspectos específicos do conforto respiratório adaptativo, mas não necessitavam de desempenho neurológico de recém-nascidos PIG, como a pes- oxigenoterapia e estavam em berço comum no momento do quisa de avaliação do tônus muscular por método objetivo, exame. indicam a presença
Recommended publications
  • Hypotonia and Lethargy in a Two-Day-Old Male Infant Adrienne H
    Hypotonia and Lethargy in a Two-Day-Old Male Infant Adrienne H. Long, MD, PhD,a,b Jennifer G. Fiore, MD,a,b Riaz Gillani, MD,a,b Laurie M. Douglass, MD,c Alan M. Fujii, MD,d Jodi D. Hoffman, MDe A 2-day old term male infant was found to be hypotonic and minimally abstract reactive during routine nursing care in the newborn nursery. At 40 hours of life, he was hypoglycemic and had intermittent desaturations to 70%. His mother had an unremarkable pregnancy and spontaneous vaginal delivery. The mother’s prenatal serology results were negative for infectious risk factors. Apgar scores were 9 at 1 and 5 minutes of life. On day 1 of life, he fed, stooled, and voided well. Our expert panel discusses the differential diagnosis of hypotonia in a neonate, offers diagnostic and management recommendations, and discusses the final diagnosis. DRS LONG, FIORE, AND GILLANI, birth weight was 3.4 kg (56th PEDIATRIC RESIDENTS percentile), length was 52 cm (87th aDepartment of Medicine, Boston Children’s Hospital, d e percentile), and head circumference Boston, Massachusetts; and Neonatology Section, Medical A 2-day old male infant born at Genetics Section, cDivision of Child Neurology, and 38 weeks and 4 days was found to be was 33 cm (12th percentile). His bDepartment of Pediatrics, Boston Medical Center, Boston, limp and minimally reactive during physical examination at birth was Massachusetts routine care in the newborn nursery. normal for gestational age, with Drs Long, Fiore, and Gillani conceptualized, drafted, Just 5 hours before, he had an appropriate neurologic, cardiac, and and edited the manuscript; Drs Douglass, Fujii, and appropriate neurologic status when respiratory components.
    [Show full text]
  • Hypotonia Surestep Product Catalog Page 29 in Step with Pediatric Hypotonia
    SPECIAL EDUCATIONAL SERIES DIAGNOSTIC INSIGHTS ANALYZING GAIT CHANGES GROSS MOTOR SKILLS ORTHOTIC MANAGEMENT CLI N I CAL CASE STUDIES Sponsored by an educational grant from: In Step With Pediatric Hypotonia SureStep Product Catalog Page 29 In Step With Pediatric Hypotonia Contents VIEWPOINT FROM THE EDITOR: An Unexpected Path, Mobility and More an Invaluable Perspective At the most basic level, mobility is about get- PAGE 3 ting from point A to point B. But, for many children with hypotonia, it’s about so much 4 more. FEATURES It’s about independence. It’s about con- fidence. It’s about maintaining strength, fit- ness, and healthy bones. It’s about not being Understanding Hypotonia excluded from activities enjoyed by their PAGE 4 typically developing peers. And improved mobility may have even Gait: The Cornerstone more benefits in those children whose hy- potonia is associated with social and behav- of Intervention ioral developmental delays. New research PAGE 8 has identified an association between motor skills and sociobehavioral milestones in chil- 8 The Importance of Gross dren with autism spectrum disorder, who often present with hypotonia (see “The Im- Motor Skills portance of Gross Motor Skills,” page 12). PAGE 12 This suggests that early intervention to improve gross motor skills—including or- thotic devices and physical therapy—may Orthotic Solutions for also help certain children interact more Children with Hypotonia comfortably with others. That won’t come as PAGE 16 a surprise to the clinicians and parents who 12 have personally seen it happen. This special issue is filled with evidence- Orthotic Success Stories: based information and personal success sto- Four Cases in a Series ries illustrating how effective interventions can enhance mobility in children with hy- PAGE 20 potonia.
    [Show full text]
  • IUGR: Intrauterine Growth Restriction
    Table S1. Clinical features observed in the 6 patients described so far harboring pathogenic variants in FOXRED1. Evolutionary symptoms Variants Prenatal Onset Onset clinical Patient Lactic/ Survival FOXRED1 period age symptoms Muscular Psychomotor Metabolic Epilepsy MRI Visual Respiratory Cardiovascular Others tone development acidosis IUGR 2m Hypotonia Yes (+++) Yes ↓ Normal Latent Bronchospasm Normal AEP normal IQ: 48 Alive c.920G>A Development refractary (2m,4y,7y3m) strabismus of episodes in (15y) 1 (p.Gly307Glu) / al delay right eye infant c.733+1G>A c.920G>A NI 4y Clumsiness With No Normal Normal Normal Normal Normal Learning IQ: 99 Alive 2 (p.Gly307Glu) / exercise (+) disorders (19y) c.733+1G>A - Neonatal Premature; No (only ↑ Yes ↓ Decreased Normal Normal Normal Normal Gradually loss Alive period Hypoglycemia lactate in attenuation in of motor (22y)) Congenital LCR) the putamen skills; c.694C>T lactic acidosis and cerebellar wheelchair; (p.Gln232X) / 3 atrophy (6y) no expressive c.1289A>G language; 18 (p.Asn430Ser) understands simple commands NI Neonatal Truncal Yes Yes ↓ Delayed Eye Normal Mild non- Persistent Psychomotor Alive period hypotonia myelination movements obstructive left hepatomegaly retardation (10y) c.1054 C>T Poor feeding ventricular have always ventricular (p.Arg352Trp) / dilatation; been roving hypertrophy 4 c.1054 C>T abnormal signal bilateral optic (p.Arg352Trp) 19 in the thalami atrophy and basal ganglia (8m) c.1308G>A ND ND ND ND Yes NA NA NA NA NA NA Severe Alive (p.Val421Met) / psychomotor (¿) 5 c.1308G>A retardation (p.Val421Met)20 IUGR; Neonatal Congenital Yes Yes ↓ Large -- Persistent Dilated right - - Death (3 c.612_615dupA Cerebral period lactic periventricular severe ventricle and months) CTG intraventric acidosis.
    [Show full text]
  • Cerebral Hypotonia by Mihee Bay MD (Dr
    Cerebral hypotonia By Mihee Bay MD (Dr. Bay of Kennedy Krieger Institute and Johns Hopkins School of Medicine has no relevant financial relationships to disclose.) Originally released July 12, 2006; last updated February 1, 2016; expires February 1, 2019 Introduction This article includes discussion of cerebral hypotonia, central hypotonia, essential hypotonia, benign congenital hypotonia, and floppy infant. The foregoing terms may include synonyms, similar disorders, variations in usage, and abbreviations. Overview Hypotonia is a clinical manifestation of numerous diseases affecting the central and/or peripheral motor nervous system. The key to accurate diagnosis involves integral steps of evaluation that include a detailed history, examination, and diagnostic tests. “Cerebral” (or central) hypotonia implies pathogenesis from abnormalities from the central nervous system, and related causal disorders include cerebral dysgenesis and genetic or metabolic disorders. Patients with central hypotonia generally have hypotonia without associated weakness, in contrast to the peripheral (lower motor neuron) causes, which typically produce both hypotonia and muscle weakness. Hypotonia is a clinical manifestation of over 500 genetic disorders; thus, a logical, stepwise approach to diagnosis is essential. With recent advances in the field of genetic testing, diagnostic yield will undoubtedly improve. There is no cure, but treatment includes supportive therapies, such as physical and occupational therapy, and diagnosis-specific management. Key points • Hypotonia is reduced tension or resistance of passive range of motion. • The first step in the evaluation of a child with hypotonia is localization to the central (“cerebral”) or peripheral nervous system, or both. • Central hypotonia is more likely to be noted axially with normal strength and hyperactive to normal deep tendon reflexes.
    [Show full text]
  • Mean Platelet Volume in Asymptomatic Chorioamnionitis-Exposed Infants
    www.jpnim.com Open Access eISSN: 2281-0692 Journal of Pediatric and Neonatal Individualized Medicine 2021;10(1):e100132 doi: 10.7363/100132 Received: 2019 Aug 22; revised: 2020 Jan 26; accepted: 2020 Feb 02; published online: 2020 Dec 28 Original article Mean platelet volume in asymptomatic chorioamnionitis- exposed infants. A retrospective case-control study Atef Alshafei, Moustafa Hassan, Yaser El saba, Anwar Khan, Mahmoud Ahmed Neonatology Section, Pediatric Department, Dubai Hospital, Dubai, UAE Abstract Introduction: Maternal chorioamnionitis (CA) is a serious condition causing several neonatal morbidities and long-term neurodevelopmental sequelae in exposed infants. Current guidelines still recommend admission, laboratory evaluation, and antibiotic administration to all CA-exposed infants. The incidence of early-onset neonatal sepsis (EOS) is currently low, owing to the routine intrapartum antibiotic administration to mothers identified to be at risk of developing CA. New diagnostic tools for early diagnosis of sepsis in apparently healthy infants exposed to maternal CA are needed. Previous studies showed that mean platelet volume (MPV) is evolving as a potential inflammatory marker of neonatal sepsis. We aimed to study whether MPV can be used as an adjuvant diagnostic tool for EOS in asymptomatic CA-exposed infants. Objective: To evaluate the role of MPV as an adjuvant biomarker of EOS in cases of asymptomatic CA-exposed infants. Design: Retrospective case-control study. Setting: A tertiary care Neonatal Intensive Care Unit (NICU). Patients: Asymptomatic CA-exposed infants 37-40 weeks of gestation admitted between May 2016 and April 2019 to the NICU of Dubai Hospital, UAE. Results: A total of 1,300 infants were admitted to NICU during the study period.
    [Show full text]
  • Long-Term Outcome After Neonatal Meconium Obstruction
    Long-term Outcome After Neonatal Meconium Obstruction Julie R. Fuchs, MD, and Jacob C. Langer, MD ABSTRACT. Objective. It is unclear whether children meconium ileus and those undergoing resection or enter- with cystic fibrosis (CF) who present with neonatal ostomy. Patients with meconium obstruction who do not meconium ileus have a different long-term outcome from have CF have an excellent long-term prognosis. This those presenting later in childhood with pulmonary com- information will be useful in counseling the families of plications or failure to thrive. We examined a cohort of infants presenting with neonatal meconium obstruction. patients with meconium ileus, and compared their long- Pediatrics 1998;101(4). URL: http://www.pediatrics.org/ term outcome with children who had CF without meco- cgi/content/full/101/4/e7; cystic fibrosis, meconium ileus, nium ileus and neonates who had meconium obstruction meconium plug syndrome. without CF (meconium plug syndrome). Study Design. Comparative study using retrospective and follow-up interview data. ABBREVIATION. CF, cystic fibrosis. Patients. Group 1 consisted of 35 surviving CF pa- tients who presented with meconium ileus between 1966 econium obstruction in the neonate is a and 1992. Two control groups were also studied: 35 age- spectrum of disease that includes meco- and sex-matched CF patients without meconium ileus 1 (group 2), and 12 infants presenting with meconium plug Mnium ileus and meconium plug syndrome. syndrome during the same time period (group 3). Meconium ileus is characterized by extremely viscid, Outcome Measures. Pulmonary, gastrointestinal, nu- protein-rich inspissated meconium causing terminal tritional, and functional status were reviewed, and sur- ileal obstruction, and accounts for approximately gical complications were recorded.
    [Show full text]
  • Common Anomalies Associated To
    ISSN: 2643-3885 Muhsin. Int J Foot Ankle 2018, 2:013 Volume 2 | Issue 2 Open Access International Journal of Foot and Ankle RESEARCH ARTICLE Common Anomalies Associated To Congenital Vertical Talus: A Single Center Experience Elmas Muhsin* Check for Department of Medical Genetic, Afyon Kocatepe University, Turkey updates *Corresponding author: Elmas Muhsin, Department of Medical Genetic, Afyon Kocatepe University, Afyonkarahisar, Turkey vicular. The incidence is estimated to be one in 10,000. Abstract Approximately half of all cases (idiopathic) are associ- Background: Congenital vertical talus is defined as a foot deformity in which the calcaneus is in equinus, the talus is ated with deformity and 2-5 neuromuscular and genet- plantarflexed, and there is a rigid and irreducible dislocation ic disorders in the remaining cases. There is evidence of the talonavicular joint complex, with the navicular articu- that some isolated deformities are transmitted as an lating on the dorsolateral aspect of the talar neck. It is often autosomal dominant feature with incomplete pene- associated with systemic involvement. trance [1-4]. The deformity is also known by congenital Aims: To identify the most common anomalies accompany- “rocker-bottom” flatfoot because of its rigid deformity ing to CVT (Congenital Vertical Talus). No literature investi- gating similar clinical data was found in the literature review. with the forefoot dorsiflexed and the hindfoot plantar- Study design: CVT has a systemic effect and is accom- flexed. The term “congenital convex pes valgus” is also panied by many anomalies. At the same time as this study, frequently used. To make a definite diagnosis, it is im- anomalies were frequently found accompanying CVT.
    [Show full text]
  • Factors Associated with Low Muscle Tone and Impact of Common
    Original Article DOI: 10.7860/JCDR/2019/39551.12675 Factors Associated with Low Muscle Tone and Section Physiotherapy Impact of Common Musculoskeletal Problems on Motor Development in Preterm Infants at One Year of Corrected Age SRIVARSHA TELEDEVARA1, M RAJESWARI2, R SIVA KUMAR3, N UDAYAKUMAR4 ABSTRACT motor development. Backward multiple regression, Chi-square Introduction: Structural immaturity of muscular system in test Pearson’s correlation were used for data analysis. Preterm Infants (PTI) results in maturation related hypotonia Results: Backward multiple regression analysis showed which is found to be influenced by risk factors present at the statistically significant association of Birth weight, Gestational time of birth. Low muscle tone can lead to lower extremity Age, and Apgar score with low muscle tone in PTI (p<0.05). Chi- malalignment, abnormal positioning and loading resulting in square test was used to compare the muscle tone of PTI and FTI musculoskeletal problems that could have an impact on motor which showed that ATA of PTI was significantly higher than FTI development which is not well established. but within physiological limits (p<0.05). Pearson’s correlation Aim: This study was carried out to analyse the risk factors coefficient showed that there is statistically significant positive associated with low muscle tone in PTI and the impact of correlation between muscle tone and musculoskeletal problems common musculoskeletal problems on motor development of and a negative correlation between musculoskeletal problems PTI at 1 year of corrected age. and Gross Motor Quotient (GMQ) of PDMS 2 in PTI at 1 year of corrected age (p<0.05). Materials and Methods: This Cross sectional study was carried out in 36 PTI and 36 Full Term Infants (FTI) who were recruited Conclusion: Maturation related hypotonia carried during the first from Child Development unit and the details of risk factors were year of life brings about musculoskeletal problems which have obtained from the records.
    [Show full text]
  • WHO Recommendations on Interventions to Improve Preterm Birth Outcomes
    WHO recommendations on interventions to improve preterm birth outcomes For more information, please contact: Department of Reproductive Health and Research World Health Organization ISBN 978 92 4 150898 8 Avenue Appia 20, CH-1211 Geneva 27, Switzerland Fax: +41 22 791 4171 E-mail: [email protected] www.who.int/reproductivehealth WHO recommendations on interventions to improve preterm birth outcomes WHO Library Cataloguing-in-Publication Data WHO recommendations on interventions to improve preterm birth outcomes. Contents: Appendix: WHO recommendations on interventions to improve preterm birth outcomes: evidence base 1.Premature Birth – prevention and control. 2.Infant, Premature. 3.Infant Mortality – prevention and control. 4.Prenatal Care. 5.Infant Care. 6.Guideline. I.World Health Organization. ISBN 978 92 4 150898 8 (NLM Classifi cation: WQ 330)Contents © World Health Organization 2015 All rights reserved. Publications of the World Health Organization are available on the WHO web site (www.who.int) or can be purchased from WHO Press, World Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel.: +41 22 791 3264; fax: +41 22 791 4857; e-mail: [email protected]). Requests for permission to reproduce or translate WHO publications –whether for sale or for non-commercial distribution– should be addressed to WHO Press through the WHO website (www.who.int/about/licensing/copyright_form/en/index.html). The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries.
    [Show full text]
  • Neonatal Hypotonia
    Neonatal Hypotonia Clinical Approach to Floppy Baby Hypotonia in the newborn is a common presenting feature of systemic illness or neurologic dysfunction at any level of the central or peripheral nervous system. It is defined as reduced resistance to passive range of motion in joints. Etiology: diverse Causes include (but are not limited to): Central Sepsis (most common) Hypoxic ischemic encephalopathy Intracranial hemorrhage Cerebral malformations Chromosomal abnormalities (e.g.Trisomy 21, Prader-Willi syndrome) Congenital infections (TORCH) Drug effects (e.g. benzodiazepines, Magnesium toxicity) Inborn errors of metabolism Endocrine: hypothyroidism Benign congenital hypotonia Spinal cord Birth trauma (especially Breech delivery) Syringomyelia Anterior Horn Cell Spinal Muscular Atrophy Neurogenic arthrogryposis Neuromuscular Myasthenia gravis (transient/ congenital) junction Infantile botulism Peripheral nerves Congenital hypomyelinating neuropathy Hereditary motor and sensory neuropathies (Dejerine-Sottas disease) Hereditary sensory and autonomic neuropathy Guillain Barre syndrome (very rare) Muscle Congenital myopathies (e.g. central core disease, Nemaline Rod myopathy, myotubular myopathy, congenital fiber type disproportion and multicore myopathy) Congenital muscular dystrophies( merosin deficient, Walker- Warburg disease, muscle-eye-brain disease, Fukuyama disease Muscular dystrophies (inc. congenital myotonic dystrophy) Metabolic myopathies Disease of Glycogen Metabolism and multisystem Acid maltase deficiency
    [Show full text]
  • Review and Hypothesis: Syndromes with Severe Intrauterine Growth
    RESEARCH REVIEW Review and Hypothesis: Syndromes With Severe Intrauterine Growth Restriction and Very Short Stature—Are They Related to the Epigenetic Mechanism(s) of Fetal Survival Involved in the Developmental Origins of Adult Health and Disease? Judith G. Hall* Departments of Medical Genetics and Pediatrics, UBC and Children’s and Women’s Health Centre of British Columbia Vancouver, British Columbia, Canada Received 4 June 2009; Accepted 29 August 2009 Diagnosing the specific type of severe intrauterine growth restriction (IUGR) that also has post-birth growth restriction How to Cite this Article: is often difficult. Eight relatively common syndromes are dis- Hall JG. 2010. Review and hypothesis: cussed identifying their unique distinguishing features, over- Syndromes with severe intrauterine growth lapping features, and those features common to all eight restriction and very short stature—are they syndromes. Many of these signs take a few years to develop and related to the epigenetic mechanism(s) of fetal the lifetime natural history of the disorders has not yet been survival involved in the developmental completely clarified. The theory behind developmental origins of origins of adult health and disease? adult health and disease suggests that there are mammalian Am J Med Genet Part A 152A:512–527. epigenetic fetal survival mechanisms that downregulate fetal growth, both in order for the fetus to survive until birth and to prepare it for a restricted extra-uterine environment, and that these mechanisms have long lasting effects on the adult health of for a restricted extra-uterine environment [Gluckman and Hanson, the individual. Silver–Russell syndrome phenotype has recently 2005; Gluckman et al., 2008].
    [Show full text]
  • AMERICAN ACADEMY of PEDIATRICS Management of Hyperbilirubinemia in the Newborn Infant 35 Or More Weeks of Gestation
    AMERICAN ACADEMY OF PEDIATRICS CLINICAL PRACTICE GUIDELINE Subcommittee on Hyperbilirubinemia Management of Hyperbilirubinemia in the Newborn Infant 35 or More Weeks of Gestation ABSTRACT. Jaundice occurs in most newborn infants. Hyperbilirubinemia”3 for a description of the meth- Most jaundice is benign, but because of the potential odology, questions addressed, and conclusions of toxicity of bilirubin, newborn infants must be monitored this report.) This guideline is intended for use by to identify those who might develop severe hyperbili- hospitals and pediatricians, neonatologists, family rubinemia and, in rare cases, acute bilirubin encephalop- physicians, physician assistants, and advanced prac- athy or kernicterus. The focus of this guideline is to tice nurses who treat newborn infants in the hospital reduce the incidence of severe hyperbilirubinemia and bilirubin encephalopathy while minimizing the risks of and as outpatients. A list of frequently asked ques- unintended harm such as maternal anxiety, decreased tions and answers for parents is available in English breastfeeding, and unnecessary costs or treatment. Al- and Spanish at www.aap.org/family/jaundicefaq. though kernicterus should almost always be prevent- htm. able, cases continue to occur. These guidelines provide a framework for the prevention and management of DEFINITION OF RECOMMENDATIONS hyperbilirubinemia in newborn infants of 35 or more The evidence-based approach to guideline devel- weeks of gestation. In every infant, we recommend that clinicians 1) promote and support successful breastfeed- opment requires that the evidence in support of a ing; 2) perform a systematic assessment before discharge policy be identified, appraised, and summarized and for the risk of severe hyperbilirubinemia; 3) provide that an explicit link between evidence and recom- early and focused follow-up based on the risk assess- mendations be defined.
    [Show full text]