Abstract Increasing evidence suggests that early-life exposures influence the health and wellbeing in later life. Preterm birth (before 37 weeks of gestation) is associated with an increased risk of cardiometabolic disorders in later life. This risk may be partly mediated by nutrition along the course of life. As a part of the Helsinki Study of Very Low Birth Weight Adults, the aim of the present work was to investigate the association between energy and macronutrient intake during the first weeks after preterm birth at very low birth weight (VLBW, birthweight < 1500g) and body composition and energy metabolism in adulthood (n=127). A further aim was to examine traits related to eating disorders and food and nutrient intake in young adults born early (<34 weeks of gestational age, n=191) and late (34-<37 weeks of gestational age, n=364) preterm and term-born controls (n=657) from the ESTER study and Arvo Ylppö Longitudinal study. Relatively low neonatal energy and nutrient intakes during the first weeks of life of infants born at VLBW predicted body composition and energy metabolism in adulthood. When adjusted for sex, age, gestational age and birth-weight SD score every 1g/kg/day greater early protein intake was associated with 10.4% (95% CI 2.4, 19.1) higher lean body mass (LBM) and 8.5% (0.2, 17.0) higher resting energy expenditure (REE). The ratio of REE/LBM however was 5.5% (0.8, 10.0) lower. In addition, higher protein and energy intakes predicted lower energy intake per unit of LBM in young adults. These associations were only partly mediated by early growth. Young women born early preterm reported on average healthier body image and fewer traits related to eating disorders when compared with term-born peers. However, their adherence to recommended eating guidelines was on average lower. According to the results of present work, energy balance is partly programmed by relatively small variations in the amount of protein in the diet in infancy. Among young adults born preterm, focusing on primary prevention, such as dietary counseling, is suggested. / Tiivistelmä Elämän varhaisvaiheet muokkaavat terveyttä ja hyvinvointia pitkällä aikavälillä. Ennenaikaisesti (ennen 37. raskausviikkoa) syntyneillä aikuisilla on todettu olevan suurempi riski sairastua sydän- ja verisuonitauteihin verrattuna täysiaikaisina syntyneisiin ikätovereihin. Ravitsemuksella, läpi elämänkaaren, on keskeinen rooli tuon riskin muokkaajana. Tämän väitöskirjatutkimuksen tavoitteena oli selvittää osana Pikku-k-tutkimusta (n=127), miten pienipainoisina (syntymäpaino <1500g) syntyneiden keskosten elämän ensimmäisten viikkojen energian ja ravintoaineiden saanti ennustaa kehonkoostumusta ja energiankulutusta sekä energian saantia aikuisiässä. Lisäksi tavoitteena oli tutkia ESTER- tai AYLS-kohorttitutkimuksiin osallistuneiden, hyvin (<34 raskausviikolla syntyneiden, n=191) ja lievästi (34-37, n=364) keskosena syntyneiden ja täysiaikaisena syntyneiden (n=657) nuorten aikuisten syömishäiriöpiirteitä, kehonkuvaa sekä ruoan käyttöä ja ravintoaineiden saantia. Suhteellisen matala elämän ensimmäisten viikkojen aikainen energian ja ravintoaineiden saanti ennusti kehonkoostumusta ja energia-aineenvaihduntaa aikuisiässä. 1g/kg/päivä korkeampi proteiininsaanti oli yhteydessä 10,4 % (95% luottamusväli 2,4; 19,1) suurempaan rasvattomaan painoon sekä 8,5 % (0,2; 17,0) korkeampaan lepoenergiankulutukseen aikuisiässä. Lepoenergiankulutus rasvatonta painoyksikköä kohden oli kuitenkin 5,5 % (0,8; 10,0) matalampi enemmän proteiinia saaneilla keskosilla. Lisäksi korkeampi energian ja proteiininsaanti elämän ensimmäisten viikkojen aikana ennusti matalampaa energiansaantia painoyksikköä kohden aikuisiässä. Varhaisella kasvulla oli vain pieni rooli tämän yhteyden välittäjänä. Nuorilla, hyvin ennenaikaisena (ennen 34. raskausviikkoa) syntyneillä, naisilla oli vähemmän syömishäiriöihin liittyviä piirteitä ja terveellisempi kehonkuva verrattaessa heitä täysiaikaisena syntyneisiin ikätovereihin. Arvioitaessa heidän ruokavaliotaan, todettiin kuitenkin heidän syövän hieman epäterveellisemmin ikätovereihin verrattuna. Tämän väitöskirjatutkimuksen tulosten valossa varhainen puuttuminen keskosena syntyneiden lisääntyneeseen sydän- ja verisuonitautien riskiin on mahdollista kiinnittämällä huomiota varhaiseen ravitsemukseen ja varhaisen aikuisiän elintapaohjaukseen, etenkin ravitsemukseen liittyen.

Introdução: Os benefícios do leite materno na alimentação de recém-nascido pré-termo (RNPT) estão amplamente comprovados na literatura; o estabelecimento do aleitamento materno nesta população, porém, envolve vários fatores que podem dificultar esse processo. Objetivo: Analisar os padrões de aleitamento materno em recém-nascidos pré-termo internados e no primeiro mês após a alta hospitalar. Método: Estudo observacional de coorte prospectivo com 116 mães e seus recém-nascidos pré-termos internados na Unidade de Internação Neonatal (UIN) do Hospital de Clínicas de Porto Alegre (HCPA) entre 1.º de setembro de 2009 e 25 de agosto de 2010 que nascerem com idade gestacional >32 e <37 semanas, que permaneceram internados na UIN e que estavam sendo amamentados por ocasião da alta hospitalar. Os dados da pesquisa foram obtidos através de um formulário feito com base em consultas aos prontuários do bebê e da mãe, ao livro de registro e ao cadastro da nutriz do Banco de Leite Humano (BLH) e de três entrevistas realizadas com a mãe: a primeira entrevista, presencial, na véspera da alta do bebê, e a segunda e a terceira entrevistas, por telefone, respectivamente, no 14.º dia e no 28.º dia após a alta do RNPT. O projeto, aprovado pela Comissão de Ética e de Pesquisa do HCPA sob o número 09.291, foi financiado pelo Fundo de Incentivo à Pesquisa e Eventos (FIPE) do HCPA. Resultados: Os bebês incluídos no estudo apresentaram idade gestacional média de 34,5±1,4 semanas, peso médio ao nascer de 2130,5±567,7g, 59,5% do sexo masculino e mediana de tempo de internação na UIN de 15 (10-29) dias. Dentre as características das mães, destacaram-se idade média de 27,3±7,5 anos; escolaridade média de 9,4±3,4 anos; 57,8% de cor branca; 50,9% não tinham experiência prévia com amamentação. No momento da alta hospitalar, todos os bebês estavam em aleitamento materno. No 14.º dia após a alta, 36,2% dos RNPT estavam em aleitamento materno exclusivo (AME), 55,2% se encontravam em aleitamento materno e 8,6% já tinham sido desmamados. Já no 28.º dia após a alta hospitalar, 25% estavam em AME, 60,3% das crianças se encontravam em aleitamento materno e 14,7% delas estavam desmamadas. Desenvolveu-se análise multivariável separadamente com as variáveis relacionadas ao bebê e à mãe. Os resultados da análise multivariável das variáveis relacionadas ao bebê, quando ajustada para peso de nascimento, idade gestacional ao nascer, tempo de hospitalização e recebia complemento após mamar no peito na hospitalização, mostraram que o início do AME após a alta hospitalar esteve somente associado ao não uso de chupeta antes de iniciar a amamentação exclusiva (HR= 4,01; IC95%: 2,13-7,52). Já a análise multivariável dos fatores maternos, quando ajustada para bebê satisfeito mamando só no peito na percepção da mãe na hospitalização e local onde a mãe se encontrava na hospitalização do filho, revelou associação entre o início do AME após a alta hospitalar e a orientação de AME na alta hospitalar do bebê (HR=6,6; IC 95%: 2,90-15,16). Conclusões: Verificou-se que os padrões de aleitamento materno se alteraram no decorrer do primeiro mês após a alta. O AME ocorreu somente no domicílio, e seu início foi associado à orientação recebida na alta hospitalar de amamentar exclusivamente o bebê em casa e ao não uso da chupeta antes de começar o AME. Desse modo, o estudo remete à reflexão sobre a importância do seguimento do aleitamento materno e dos resultados das orientações oferecidas às mulheres no pré-natal, durante a hospitalização e no domicílio. / Background: The benefits of human milk for preterm infants are recognized in the scientific literature. However, the establishment of preterm infant breastfeeding involves many factors that complicate this process. Objective: To analyze breastfeeding patterns in hospitalized preterm babies and one month after the hospital discharge. Methods: Prospective cohort study with 116 mothers and their preterm babies hospitalized at “Hospital de Clínicas de Porto Alegre” (HCPA) Neonatal Unit from September 1st 2009 to August 25th 2010 born of a gestational age between 32 and 36 weeks, hospitalized for the entire time at HCPA Neonatal Unit and having been breastfed until the time of the hospital discharge. The variables were collected via consultation of babies’ and mothers’ medical records, registers books of human milk bank and through three interviews with the mother: the first one was personal, done right before the babies’ hospital discharge day, the second and the third ones were done by telephone, respectively, on the 14th and the 28th days after the hospital discharge. This project, approved by HCPA under number 09.291, was supported by HCPA’s Research Incentive Fund and Events. Results: The babies included in this study presented the following characteristics: average gestational age of 34.5±1.4 weeks, average birth weight of 2.130,5±567.7g, median hospital stay of 15 (10-29) days, and 59.5% were males. Among the mothers’ characteristics, we can highlight the following: average age of 27.3±7.5, average school attendance of 9.4±3.4 years; 57.8% were white; 50.9% did not have previous breastfeeding experience. At the moment of the hospital discharge, all the babies were being breastfed. On the 14th day after the hospital discharge, 36.2% were being exclusively breastfed; 55.2% were breastfed, e 8.6% had been weaned. On the 28th day after hospital discharge, 25% were exclusively breastfed, 60.3% were breastfed, and 14.7% were weaned. A multivariate analysis was separately performed with variables related to the babies and mothers. The results of the multivariate analysis with variables related of the baby, when adjusted to birth weight, gestational age at birth, hospital stay and complementary to breastfeeding during hospital stay, have shown that the beginning of exclusive breastfeeding after the hospital discharge was only associated with non-use of pacifier before the beginning of exclusive breastfeeding (HR= 4,01; IC95%: 2,13-7,52). The multivariate analysis of the mother’s factors, when adjusted to baby satisfied only with breastfeeding during hospital stay according to mother’s perception and place where the mother was during her child’s hospital stay, has shown association between the beginning of exclusive breastfeeding after the hospital discharge with recommendation of exclusive breastfeeding at the baby’s hospital discharge (HR=6,6; IC 95%: 2,90-15,16). Conclusions: It was found that the patterns of breastfeeding changed along the first month after the hospital discharge. Exclusive breastfeeding occurred only at home, and its beginning was associated with the recommendation at hospital discharge of offering only breast milk to the baby at home and not offering the pacifier before initiating exclusive breastfeeding. Therefore, this study has led us to the reflection on the importance of both proceeding with breastfeeding and the results of recommendations given to the women along the pre-natal period, during hospital stay and at home. / Introducción: Los beneficios de la leche materna en la alimentación del recién nacido prematuro (RNPT) están ampliamente comprobados en la literatura, sin embargo, el establecimiento de la lactancia en esta población envuelve varios factores que pueden dificultar ese proceso. Objetivo: Analizar los padrones de lactancia materna en recién nacidos prematuros internados y durante el primer mes después del alta del hospital. Método: Estudio observacional de corte prospectiva con 116 madres y sus recién nacidos prematuros internados en la Unidad de Internación Neonatal (UIN) del Hospital de Clínicas de Porto Alegre (HCPA) entre el 1º de Septiembre del 2009 al 25 de Agosto del 2010 que nacieron con edad gestacional > 32 y < 37 semanas, que permanecieron internados en la UIN y que estaban siendo amamantados por ocasión del alta del hospital. La colecta de datos del estudio fue realizada a través de un formulario elaborado con base en consultas a la ficha médica del bebé y de la madre, al libro de registro y al catastro de la Nutriz del Banco de Leche Humano (BLH) y de tres entrevistas realizadas con la madre; la primera entrevista, presencial, a vísperas del alta del bebé; la segunda y la tercera entrevistas, por teléfono, ocurriendo estas, respectivamente, al 14º día y al 28º día después del alta del RNPT. El proyecto, aprobado por la Comisión de Ética y de Investigación del HCPA, sobre el número 09.291, fue financiado por el Fondo de Incentivo a la Investigación y Eventos del HCPA. Resultados: Los bebés incluidos en el estudio presentaron edad gestacional media de 34,5±1,4 semanas, peso medio al nacer de 2130,5±567,7g, 59,5% de sexo masculino y mediana de tiempo de internación en la UIN de 15 (10-29) días. Entre las características de las madres, se destacaron edad media de 27,3±7,5 años; escolaridad media de 9,4±3,4 años; 57,8% de color blanca; 50,9% no tenían experiencia previa con lactancia materna. En el momento del alta del hospital, todos los bebés estaban en lactancia materna. En el 14.º día después del alta, 36,2% estaban siendo amamantados de pecho exclusivamente (AME); 55,2%, en lactancia materna, y 8,6% ya habían sido desmamados. Ya al 28º día después del alta del hospital, 25% se encontraban en AME, 60,3% de los niños estaban en lactancia materna y 14,7% de ellos estaban desmamados. Se efectuó un análisis multivariable separadamente con las variables relacionadas al bebé y a la madre. Los resultados del análisis multivariable de las variables relacionadas al bebé, cuando ajustado para peso de nacimiento, edad gestacional al nacer, tiempo de hospitalización y recebía fórmula después de mamar en el seno durante la hospitalización, mostraron que el inicio del AME después del alta del hospital estuvo solamente asociado al no uso de chupeta antes de iniciar la lactancia exclusiva (HR=4,01; IC95%: 2,13-7,52). Ya el análisis multivariable de los factores maternos, cuando ajustado para bebé satisfecho mamando solo en el pecho en la percepción de la madre durante la hospitalización y local donde la madre se encontraba en la hospitalización del hijo, reveló asociación entre el inicio del AME después del alta del hospital y la orientación de AME en el alta del hospital del bebé (HR=6,6; IC 95%: 2,90-15,16). Conclusiones: Se verificó que los padrones de lactancia se alteraron durante el transcurso del primer mes después del alta. El AME ocurrió solamente en el domicilio, y su inicio fue asociado a orientación recibida durante el alta del hospital de amamantar exclusivamente al bebé en casa y al no uso da chupeta antes de comenzar o AME. De ese modo, el estudio lleva a la reflexión sobre la importancia del seguimiento de la lactancia materna y de los resultados de las orientaciones ofrecidas a las mujeres en el pre-natal, durante la hospitalización y a domicilio.

>Magister Scientiae - MSc / The aim of this study was to compare the trough plasma levels of Aspen-Vancomycin® (AV); and Sandoz-Vancocin CP® (SV) in premature infants with suspected Methicillin Resistant Staphylococcus aureus (MRSA) infection. The study was designed as a prospective, double blind, randomised trial involving male and female premature infants admitted in the Neonatal Intensive care Unit (NICU) at Netcare Blaauwberg and N1-city Hospitals for treatment of suspected MRSA-infection between April 2012 and June 2013. The inclusion criteria were: 29-35 weeks postmenstrual age (PMA), informed and written consent from parents of each premature infant enrolled in the study. Blood samples (0.3-0.4ml) were collected for renal function test and vancomycin trough levels determination. Blood samples for vancomycin trough level assay were collected thirty minutes prior to the administration of the third dose of vancomycin. Statistical analysis was performed and estimation was made giving an indication of how many infants will be needed to make the study statistically significant. Wilcoxon Two-Sample test was performed to determine the p-values and Spearman correlation coefficients were used to determine the correlation between trough levels and variables. P-values < 0.05 were considered significant. A total of 19 premature infants met with study criteria, 10 (5 females and 5 males) received AV and 9 (6 females and 3 males) receive d SV. There was no statistical significant difference between the demographic (GA, BW, PMA, PNA, weight at trial entry, height at trial entry) and biological (albumin, serum creatinine concentration and glomerular filtration rate) parameters of the premature infants in the AV and SV group. There were no statistical significant difference between trough level 1 of AV and SV, although trough level 1 had a lower trend in the SV group (p=0.118). No AV trough level 1 was below the minimum effective concentration (<5μg/ml). It was found that 30% of AV trough level 1 was within the therapeutic range (5-10μg/ml) and 70% of AV trough level 1, were above minimum toxic concentration (>10mg/l). It was found that 22.2% of SV trough level 1 was below minimum effective concentration, 44.4% of SV trough level 1 was within therapeutic range and 33.3% of trough level 1 was above minimum toxic concentration. No correlation was found between trough level 1 and the demographic and biological parameters of the premature infants in the AV group. SV had a positive correlation with GA, BBW, PMA and a negative correlation with PNA

Introdução: O aperfeiçoamento da assistência pré-natal e dos cuidados intensivos neonatais contribuiu para a redução da mortalidade dos recémnascidos (RN) com riscos para alterações do desenvolvimento neuromotor. Apesar destes avanços, a difícil previsão e prevenção de danos neurológicos está associada ao aumento de crianças com problemas graves como a Paralisia Cerebral (PC). Das avaliações disponíveis atualmente, a que possui melhor valor preditivo de danos neurológicos em bebês até os cinco meses de idade é a \"Avaliação Qualitativa dos Movimentos Generalizados (MGs)\" de Prechtl. No entanto, apresenta pouca aderência na prática clínica devido à sua subjetividade e necessidade de treinamento prévio para aplicação. Objetivos: Desenvolver e analisar a confiabilidade de uma escala de avaliação baseada nos MGs caracterizados a partir da avaliação qualitativa de Prechtl em recémnascidos e lactentes com riscos para alterações no desenvolvimento neuromotor. Método: Estudo observacional transversal com a participação de 30 RNs e lactentes com idade compreendida entre 31 semanas pós-menstrual e 17 semanas pós-termo avaliados no Hospital Universitário da USP. Os MGs normais e anormais foram avaliados segundo a análise qualitativa dos MGs de Prechtl seguindo as três fases: pré-termo (n=7), writhing movements (n=13) e fidgety movements (n=10). A escala foi construída baseando-se nestas fases e foram elaboradas duas versões, sendo analisadas as confiabilidades inter e intra-examinador por meio do ICC e do índice de Kappa. A consistência interna da versão final foi analisada através do alfa de Cronbach. Resultados: Foram analisadas duas versões da escala com três diferentes sistemas de pontuação: respostas do tipo \"SIM ou NÃO\"; do tipo \"SEMPRE, ALGUMAS VEZES e NUNCA\"; e \"SEMPRE, QUASE SEMPRE, ALGUMAS VEZES, QUASE NUNCA E NUNCA\". Os resultados mais significativos foram obtidos com as respostas binárias (SIM ou NÃO), sendo que nas fases pré-termo e writhing movements a pontuação máxima é de 32 pontos e na fase dos fidgety movements é de 12 pontos. A análise da confiabilidade da versão final da escala evidenciou concordância excelente tanto para a confiabilidade intra-avaliador (ICCs: 0.914 a 0.999; Kappa: 0.6 a 1 e 0.606 a 1, considerando a escala binária), como para confiabilidade inter-avaliadores (ICCs: 0.871 a 0.966 para avaliação 1; Kappa: 0.682 a 0.775 para avaliação 1, considerando novamente a escala binária). Apenas o índice Kappa neste caso apresentou concordância boa. Os valores de alfa de Cronbach se mostraram de bons a excelentes (0.866 a 0.980). Verificou-se também que os bebês com MGs anormais apresentaram pontuação abaixo de valores entre 20 e 25 na fase pré-termo e dos writhing movements, e abaixo de valores entre 8 e 12 na fase dos fidgety movements. Conclusão: Foi possível desenvolver uma escala capaz de quantificar os MGs, com pontuação capaz de diferenciar MGs normais de anormais, com excelente confiabilidade inter e intra-avaliador e alta consistência interna. A escala apresenta grande relevância clínica e, aliada ao treinamento no método qualitativo, torna-se um instrumento promissor para a detecção precoce de riscos para atraso do desenvolvimento neuromotor e seleção dos RNs e lactentes para acompanhamento e intervenção precoce / Introduction: The technological improvement of neonatal care and intensive care contributed to reduction of preterm newborn (PTNB) mortality. Despite these improvements, is still difficult to predict and prevent neural damage and neurobehavioral impairments, which are associated to higher proportion of children with severe neurological problems, such as Cerebral Palsy (CP). Between all the available methods of babies\' assessment and examination, the Prechtl´s Method of Qualitative Assessment of General Movements (GMs) shows the higher predictive value to neurological damage. Nevertheless, this assessment is not widely used because of its subjectivity and the necessity of training of the examiners. Objective: To develop a quantitative scale based on GMs in the newborn and infant, and to verify its reliability. Method: Crosssectional observational study involving 30 newborns and infants aged between 31 weeks postmenstrual age and 17 weeks post term age assessed at university hospital of University of São Paulo. The normal and abnormal GMs were evaluated based on the Prechtl´s Method of Qualitative Assessment of GMs following the three phases: preterm GMs (n=7), writhing movements (n=13) and fidgety movements (n=10). The scale was developed based on these phases and Kappa and ICC statistics were applied in the reliability analysis (inter- and intra-observer agreement). Cronbach alpha was applied in the internal consistency analysis. Results: Two versions of the scale were analyzed with three different scoring systems: \"YES or NO\"; \"ALWAYS, SOMETIMES and NEVER; \"ALWAYS, OFTEN, SOMETIMES, ALMOST NEVER and NEVER\". The most significant results were obtained with \"YES or NO\" answers. The total score obtained in preterm and writhing movements phases was 32 points and in the fidgety movements phase was 12 points. Considering the assessment with the final version of the scale, high to very high inter- (ICCs 0.871-0.966; Kappa 0.682-0.775 for the first evaluation, considering \"YES or NO\" answers) and intra-observer reliability (ICCs: 0.914-0.999; Kappa: 0.6-1, considering \"YES or NO\" answers) was found. High to very high Cronbach alpha values was also found (0.866-0.980). The infants showed abnormal GMs score below values between 20 and 25 in preterm phase and writhing movements, and below values between 8 and 12 at fidgety movements age. Conclusion: It was possible to develop a scale able to quantify GMs, with scores that can differentiate normal from abnormal GMs, with excellent inter- and intra-observer reliability and internal consistency. The scale has great clinical relevance and, combined with training in qualitative method, it is a promising tool for early detection of risks for delayed neuromotor development and screening of newborns and infants for monitoring and early intervention

Introduction. L’exposition à la douleur répétée pendant la période néonatale a des effets nocifs sur le développement neurologique des nouveau-nés prématurés et peut contribuer à une douleur prolongée. Une taxonomie précise de la douleur néonatale est absente due à l’existence d’une terminologie ambigüe qui persiste en néonatologie. Par conséquent, l’évaluation et la gestion de ce type de douleur dans le milieu clinique sont sous-optimales. Objectif. Établir la portée, l'étendue et la nature des écrits scientifiques liées à la douleur prolongée des nouveau-nés prématurés hospitalisés dans l’unité de soins intensifs néonatals (USIN), par le biais d’une revue de la portée. Méthodologie. La revue de la portée suit les lignes directrices du Joanna Briggs Institute (JBI). Une stratégie de recherche a été effectuée dans les bases de données CINAHL, PubMed, Medline, Web of Science, Google Scholar, GeryLit.org et Grey Source Index. Résultats. La revue de la portée a identifié 78 articles pertinents qui abordaient des définitions (n=25), des indicateurs (n=37), des contextes de soins (n=47), des outils d’évaluation (n=49), des conséquences (n=29) et des interventions (n=21) pour soulager la douleur prolongée néonatale. La revue soutien que les contextes de soins des nouveau-nés prématurés devraient toujours être considérés indépendamment de la présence ou non d’indicateurs de la douleur prolongée afin de guider l’évaluation et le soulagement de la douleur prolongée. Conclusion. Ce mémoire a recensé les éléments essentiels de la douleur prolongée et a permis d’émettre des recommandations pour la pratique, la formation, la gestion et le recherche infirmière, guidé par le cadre théorique de Huth et Moore (1998). / Introduction. Exposure to repetitive pain during the neonatal period has been shown to have important long-term effects on the neurodevelopment of the premature neonate and can contribute to experienced prolonged pain. Since a uniform taxonomy of neonatal prolonged pain is still lacking to this day in neonatology, prolonged pain management remains suboptimal in neonatal intensive care units (NICU). Aim. This master’s thesis aims to determine the scope, extent, and nature of the available literature on prolonged pain in premature neonates hospitalized in the NICU by way of a scoping review. Methodology. An electronic search was conducted in the databases of CINAHL, PubMed, Medline, Web of Science, GeryLit.org and Grey Source Index. This scoping review follows the JBI guidelines for scoping reviews. Results. A total of 78 articles were included in the scoping review which identified key elements of neonatal prolonged pain such as definitions (n=25), indicators (n=37), contexts (n=47), pain scales (n=49), consequences (n=29) and possible interventions (n=21) for prolonged pain management. The contexts of care were identified as being more indicative of prolonged pain and should guide pain evaluation and management. Conclusion. This master’s thesis contributes to the foundation of growing knowledge in neonatal prolonged pain and sheds light on the ambiguity that currently exists on this topic in the scientific literature and informs nursing prolonged pain management in NICU with the ultimate goal of improving developmental outcomes of premature neonates.

<p>Uvod: Infertilitet se defini&scaron;e kao bezuspe&scaron;na koncepcija nakon jedne godine seksualnih odnosa bez upotrebe kontracepcije u fertilnoj fazi menstrualnog ciklusa. Metode asistirane reprodukcije predstavljaju efektivan način lečenja infertiliteta. Ispitivanje i identifikacija kratkoročnih i dugoročnih efekata arteficijalnih reproduktivnih tehnologija je veoma izazovan zadatak. Prvenstveni razlog tome je velika heterogenost u načinu sakupljanja, obrade, klasifikacije i tumačenja, sada već, obilja informacija koje su prikupljene u različitim istraživanjima. Individualni pristup lečenju neplodnosti, brz napredak i stalne promene u metodologiji arteficijalnih reproduktivnih tehnologija, uz ranije navedene pote&scaron;koće u vezi sa prikupljanjem i analizom podataka, značajno otežavaju precizno sagledavanje svih mogućih rizika i posledica arteficijanog začeća. Uprkos brojnim istraživanjima, naučnim publikacijama i akumuliranim dokazima, ostale su mnoge dileme u vezi odgovora na pitanja - da li su arteficijalno začete trudnoće u većoj meri praćene rizicima za neadekvatan razvoj ploda, lo&scaron;ijim perinatalnim ishodom i kakve su dugoročne posledice po decu, kao i da li su ovi rizici podjednako zastupljeni u jednoplodnim i vi&scaron;eplodnim trudnoćama.<br />Cilj rada: Ciljevi rada su bili da se utvrdi struktura morbiditeta kod prevremeno rođene dece začete vantelesnom oplodnjom (iz jednoplodnih i vi&scaron;eplodnih trudnoća) u prve dve godine života, te da se identifikuju perinatalni faktori koji su povezani sa pojavom akutnih i hroničnih komplikacija i oboljenja kod prevremeno rođene dece začete vantelesnom oplodnjom. Takođe, cilj rada je bio da se utvrde karakteristike psihomotornog razvoja kod prevremeno rođene dece začete vantelesnom oplodnjom na kraju dvanestog, osamnaestog i dvadesetčetvrtog meseca života, kao i da se identifikuju specifični faktori rizika za nepovoljan telesni, neurolo&scaron;ki i psiholo&scaron;ki ishod lečenja kod prevremeno rođene dece začete vantelesnom oplodnjom.<br />Materijal i metode: U studiju su uključena prevremeno rođena deca koja su bila hospitalizovana u Službi za neonatologiju i intenzivnu i poluintenzivnu negu i terapiju, i koja su nakon toga, tokom prve dve godine života redovno praćena u neonatolo&scaron;koj ambulanti Instituta za zdravstvenu za&scaron;titu dece i omladine Vojvodine u Novom Sadu. Retrospektivnim delom studije su obuhvaćena deca koja su lečena u Službi i praćena u neonatolo&scaron;koj ambulanti, a koja su rođena počev od 01. 01. 2011. do 31.12.2012. godine i praćena do navr&scaron;ena puna 24 meseca života. Podaci o pacijentima koji su uključeni u retrospektivni deo istraživanja prikupljani su pregledom medicinske dokumentacije. U prospektivni deo studije su uključena deca koja su lečena u Službi i koja su praćena u neonatolo&scaron;koj ambulanti, a koja su rođena između 01.01. 2013.godine i 31.12.2014. godine i potom praćena do navr&scaron;enih 24 meseca života. Iz navedene kohorte, formirane se dve grupe: Ispitivana grupa (Grupa 1) je obuhavatila svu prevremeno rođenu decu začetu vantelesnom oplodnjom koja su bila hospitalizovana i praćena na Institutu u navedenom periodu. Kontrolna grupa (Grupa 2) obuhvatila je prevremeno rođenu decu začetu prirodnim putem. Deca iz kontrolne grupe izabrana su iz kohorte tako da njihov broj bude jednak broju dece iz ispitivane grupe. Ispitanici iz ove grupe su ujednačeni (&#39;&#39;mečovani&#39;&#39;) sa decom iz ispitivane grupe prema gestacijskoj starosti i datumu rođenja. Gestacijska starost ispitanika iz kontrolne grupe se ne razlikuje za vi&scaron;e od &plusmn; 4 dana u odnosu na decu iz ispitivane grupe. Datum rođenja ispitanika koji su uključeni u kontrolnu grupu se ne razlikuje za vi&scaron;e od &plusmn; 3 meseca u odnosu na decu iz ispitivane grupe.<br />U momentu uključivanja u studiju uzimani su sledeći anamezni podaci:<br />Podaci u vezi sa majkom, trudnoći i porođaju: starost majke u momentu koncepcije, broj prethodnih poku&scaron;aja asistirane koncepcije, stručna sprema, mesto stanovanja, hronične bolesti dijagnostikovane pre trudnoće, akutne i hronične bolesti dijagnostikovane tokom trudoće (hipertenzija, pre-eklampsija, eklampsija, o&scaron;tećenje jetre), prevremena ruptura plodovih ovojaka, primena lekova tokom trudnoće, jednoplodna ili vi&scaron;eplodna trudnoća. Podaci o poremećajima posteljice i ovojaka: ablacija, placenta previja, horioamnionitis. Podaci u vezi sa detetom: intrauterina infekcija, intrauterina restrikcija rasta, način porođaja, Apgar skor. Antropometrijski parametri (telesna masa, telesna dužina, obim glave) na rođenju i tokom perioda ambulantnog praćenja deteta. Dužina inicijalne hospitalizacije deteta. Dužina invazivne i/ili neinvazivne respiratorne potpore i oksigenoterapije. Dijagnoze na otpustu iz bolnice: prisustvo te&scaron;kih posledica prematuriteta, &scaron;to podrazumeva: intrakranijalnu hemoragiju 3. i 4. stepena (definisanu u međunarodnoj klasifikaciji bolesti &ndash; deseta revizija (MKB10) pod &scaron;ifrom P52.2), cističnu periventrikularnu leukomalaciju, retinopatiju prematuriteta, bronhopulmonalnu displaziju, nekrotizirajući enterokolitis, sepsu i/ili meningitis (mikrobiolo&scaron;ki ili klinički dijagnostikovanu). Prisustvo urođenih anomalija ili genetskih sindroma i bolesti (definisanih u MKB10 pod &scaron;iframa Q00 do Q99), kao i prisustvo urođenih bolesti metabolizma (definisanih u MKB10 pod &scaron;iframa E00 do E90).<br />U retrospektivnom delu studije, pregledani su specijalistički izve&scaron;taji iz neonatolo&scaron;ke ambulante pri posetama deteta u uzrastu deteta od 12, 18 i 24 meseca, i beleženi su sledeći podaci: sve prethodno postavljene dijagnoze koje su navedene na specijalističkim izve&scaron;tajima iz neonatolo&scaron;ke ambulante, antropometrijski prametri u momentu pregleda (telesna dužina, telesna masa i obim glave), neurolo&scaron;ki nalaz (tonus, trofika, kožni i tetivni refleksi, prisustvo lateralizacije u neurolo&scaron;kom nalazu), nalaz oftalmologa (uredan nalaz/patalo&scaron;ki nalaz), procena fine i grube motorike, govora, kognitivne funkcije i socijalnog kontakta i zbirna procena psihomotornog razvoja. U prospektivnom delu studije, pri kontrolnim pregledima u neonatolo&scaron;koj ambulanti, u uzrastu deteta od 12, 18 i 24 meseca, određivano je i beleženo sledeće: ranije postavljene dijagnoze koje su navedene u medicinskoj dokumentaciji, antropometrijski prametri u momentu pregleda (telesna dužina, telesna masa i obim glave), neurolo&scaron;ki nalaz (tonus, trofika, kožni i tetivni refleksi, prisustvo lateralizacije u neurolo&scaron;kom nalazu), nalaz oftalmologa (uredan nalaz/patalo&scaron;ki nalaz), procena fine i grube motorike, govora, kognitivne funkcije i socijalnog kontakta i zbirna procena psihomotornog razvoja.<br />Rezultati: Prosečna vednost TM ispitanika iz Grupe 1, u uzrastu od 12 meseci, bila je statistički značajno manja u odnosu na ispitanike iz Grupe 2 (Studentov t test). Prosečne vednosti TD ispitanika iz obe grupe, u uzrastu od 12 meseci, nisu se statistički značajno razlikovale (Studentov t test). Prosečne vednosti OGL ispitanika iz obe grupe, u uzrastu od 12 meseci, nisu se statistički značajno razlikovale (Studentov t test). Udeo ispitanika sa patolo&scaron;kim oftalmolo&scaron;kim nalazom nije se statistički značajno razlikovao između Grupe 1 i Grupe 2 (Fi&scaron;erov test tačne verovatnoće). Udeo ispitanika sa patolo&scaron;kim neurolo&scaron;kim nalazom nije se statistički značajno razlikovao između Grupe 1 i Grupe 2 (Hi kvadrat test). Prosečne vrednosti globalnog koeficijenta razvoja (RQ), kao i prosečne vrednosti skora za pojedine elemente za procenu razvoja (motorika, koordinacija, govor i dru&scaron;tvenost) po Brunet -L&eacute;zine skali, nisu se statistički značajno razlikovale između grupa (Studentov t test). U Grupi 1 bilo je 92 (59,740%) deteta čiji je nekorigovani RQ bio ispod 90, dok je u Grupi 2 bilo 61 (39,610%) dete čiji je nekorigovani RQ bio ispod 90. Ova razlika u broju dece sa RQ koji je ispod proseka za kalendarski uzrast je statistički značajna (Hi kvadrat test, p=0,0004). Relativni rizik za ispodprosečno postignuće na testu za procenu psihomotornog razvoja (RQ&lt;90), za decu iz Grupe 1 bio je vi&scaron;i, u odnosu na decu iz Grupe 2 (RR = 1,495; 95% CI 1,181 &ndash; 1,892). U Grupi 1, bilo je 87 (56,494%) dece koja su postigla ispodprosečne korigovane vrednosti skora na testu za procenu psihomotornog razvoja (korigovani RQ&lt;90). U Grupi 2 bilo je 69 (44,805%) dece koja su postigla ispodprosečne korigovane vrednosti skora na testu za procenu psihomotornog razvoja (korigovani RQ&lt;90). Ova razlika je statistički značajna (Hi kvadrat test, p =0,040). Relativni rizik za ispodprosečno postignuće na testu za procenu psihomotornog razvoja (korigovani RQ&lt;90), za decu iz Grupe 1 bio je vi&scaron;i, u odnosu na decu iz Grupe 2 (RR = 1,261; 95%CI 1,008 &ndash; 1,577). U kategoriji dece, koja su i pored korekcije u odnosu na GS imala ispodprosečno postignuće na testu za procenu psihomotornog razvoja, u Grupi 1 čak 81/87 (93,310%) dece je imalo vrednost korigovanog RQ &ge; 85, a u Grupi 2 ovu vrednost korigovanog RQ imalo je 60/69 (86,956%) dece.<br />Prosečne vednosti TM ispitanika iz obe grupe, u uzrastu od 18 meseci, nisu se statistički značajno razlikovale (Studentov t test). Prosečne vednosti TD ispitanika iz obe grupe, u uzrastu od 18 meseci, nisu se statistički načajno razlikovale (Studentov t test). Prosečne vednosti OGL ispitanika iz obe grupe, u uzrastu od 18 meseci, nisu se statistički značajno razlikovale (Studentov t test). Udeo ispitanika sa patolo&scaron;kim oftalmolo&scaron;kim nalazom nije se statistički značajno razlikovao između Grupe 1 i Grupe 2 (Hi kvadrat test). Udeo ispitanika sa patolo&scaron;kim neurolo&scaron;kim nalazom nije se statistički značajno razlikovao između Grupe 1 i Grupe 2 (Hi kvadrat test). Prosečne vrednosti RQ, kao i prosečne vrednosti skora za pojedine elemente za procenu razvoja (motorika, koordinacija, govor i dru&scaron;tvenost) po Brunet -L&eacute;zine skali su se statistički značajno razlikovale između grupa u uzrastu od 18 meseci (Studentov t test). U Grupi 1 bilo je 57 (37,013%) dece čiji je nekorigovani RQ bio ispod 90, dok je u Grupi 2 bilo 31 (20,130%) dete čiji je nekorigovani RQ bio ispod 90. Udeo dece sa RQ koji je ispod proseka za kalendarski uzrast je statistički značajno različit između grupa (Hi kvadrat test, p = 0,010). Relativni rizik za ispodprosečno postignuće na testu za procenu psihomotornog razvoja (nekorigovani RQ&lt;90), za decu iz Grupe 1 bio je vi&scaron;i, u odnosu na decu iz Grupe 2 (RR = 1,288; 95%CI 1,181 &ndash; 2,730). Statistički značajna razlika postojala je i kada je upoređen broj dece sa vrednostima korigovanog RQ ispod 90 u Grupi 1 i Grupi 2 (36 naspram 19 po redosledu navođenja; Hi kvardat test, p = 0,011). Relativni rizik za ispodprosečno postignuće na testu za procenu psihomotornog razvoja (korigovani RQ&lt;90), za decu iz Grupe 1 bio je vi&scaron;i, u odnosu na decu iz Grupe 2 (RR = 1,895; 95%CI 1,139 &ndash; 3,152).<br />Prosečne vednosti TM ispitanika iz obe grupe, u uzrastu od 24 meseca, nisu se statistički značajno razlikovale (Studentov t test). Prosečne vednosti TD ispitanika iz obe grupe, u uzrastu od 24 meseca, nisu se statistički značajno razlikovale (Studentov t test). Prosečne vednosti OGL ispitanika iz obe grupe, u uzrastu od 24 meseca, nisu se statistički značajno razlikovale (Studentov t test). Udeo ispitanika sa patolo&scaron;kim oftalmolo&scaron;kim nalazom nije se statistički značajno razlikovao između Grupe 1 i Grupe 2 (Hi kvadrat test). Udeo ispitanika sa patolo&scaron;kim neurolo&scaron;kim nalazom nije se statistički značajno razlikovao između Grupe 1 i Grupe 2 (Hi kvadrat test). Prosečne vrednosti RQ, kao i prosečne vrednosti skora za pojedine elemente za procenu razvoja (motorika, koordinacija, govor i dru&scaron;tvenost) po Brunet -L&eacute;zine skali, nisu se statistički značajno razlikovale između grupa, u uzrastu od 24 meseca (Studentov t test). U Grupi 1 bilo je 21 dete (13,636%) čiji je nekorigovani RQ bio ispod 90, dok je u Grupi 2 bilo 17 (11,049%) dece čiji je nekorigovani RQ bio ispod 90. Razlika u broju dece sa RQ koji je ispod proseka za kalendarski uzrast nije statistički značajna (Hi kvadrat test, p= 0,488). Statistički značajna razlika nije postojala ni kada je upoređen broj dece sa vrednostima korigovanog RQ ispod 90 u Grupi 1 i Grupi 2 (12 naspram 9 po redosledu navođenja; Hi kvardat test, p = 0,497).<br />Logističkom regresionom analizom pokazano je da su ve&scaron;tačko začeće, vi&scaron;eplodnost trudnoće i IUGR nezavisni faktori rizika za manju TM u kalendarskom uzrastu od 12 meseci. Logističkom regresionom analizom dobijena je statistički značajna korelacija između vrednosti RQ u uzrastu od 18 meseci i sledećih nezavisnih varijabli: arteficijalno začeta trudnoća i vi&scaron;eplodna trudnoća. Isptanici iz Grupe 1 i Grupe 2 nisu se statistički značajno razlikovali ni po jednom od posmatranih pokazatelja telesnog i psihomotornog razvoja u uzrastu od 24 meseca.<br />Struktura morbiditeta kod dece, tokom dvogodi&scaron;njeg perioda praćenja, nije se značajno razlikovala između grupa. Jedina razlika između grupa, konstatovana je u uzrastu od 12 i 18 meseci, bila je u učestalosti akutnih respiratornih infekcija, čija je pojava, pak, bila direktno povezana sa vi&scaron;eplodnim trudnoćama, odnosno brojem siblinga u domaćinstvu.<br />Zaključak: Prosečna starost majki dece koja su začeta IVF-om je veća od prosečne starosti majki dece koja su spontano začeta. Struktura morbiditeta majki dece koja su začeta IVF-om i majki dece koja su začeta spontanom koncepcijom je ista, ali je stopa morbiditeta veća kod majki dece koja su začeta IVF-om. Vi&scaron;eplodne trudnoće su veoma zastupljene kod začeća IVF-om. Trudnoće začete IVF-om se dominantno i skoro ekskluzivno okončavaju carskim rezom. Prevremena ruptura ovojaka ploda je česta komplikacija trudnoća koje su začete IVF-om. Stopa morbiditeta prevremeno rođene dece začete vantelesnom oplodnjom nije veća u odnosu na prevremeno rođenu decu začetu prirodnim putem. U strukturi morbiditeta kod dece koja su začeta vantelesnom opodnjom, zastupljena su ista oboljenja i komplikacije kao kod prevremeno rođene dece začete prirodnim putem. Incidencija pojedinih oboljenja je ista, sa izuzetkom bronhopulmonalne displazije koja se javlja če&scaron;če kod dece začete vantelesnom oplodnjom i retinopatije prematuriteta koja se javlja če&scaron;če kod dece začete prirodnim putem. Porođajna telesna masa, intrauterina restrikcija rasta, starost majke, stručna sprema majke, prethodna hronična oboljenja majke, bolesti majke dijagnostikovane tokom trudnoće, jednoplodna i vi&scaron;eplodna trudnoća, način porođaja i PROM su potencijalni faktori rizika za lo&scaron;iji postnatalni ishod kod dece iz arteficijalno začetih trudnoća. U uzrastu od 12 meseci, prevremeno rođena deca začeta tehnikama in vitro fetrilizacije, sem po dostignutoj telesnoj masi, ne razlikuju se značajno po drugim telesnim karakteristikama, od prevremeno rođene dece koja su začeta prirodnim putem. Faktori rizika za manju telesnu masu kod prevremeno rođene dece, u uzrastu od 12 meseci su: arteficijalno začeće, vi&scaron;eplodne trudnoće i intrauterina restrikcija rasta. U uzrastu od 12 meseci, prevremeno rođena deca začeta in vitro fertilizacijom, imaju blago lo&scaron;ije (ali ne i značajno niže) postignuće na testovima za procenu psihomotornog razvoja, odnosno imaju vi&scaron;i rizik da postignu ispodprosečne vrednosti skora na testu za procenu psihomotornog razvoja. U uzrastu od 18 meseci, nema razlike u pokazateljima telesnog razvoja između prevremeno rođene dece koja su arteficijalno začeta i dece koja su rođena iz spontano začetih trudnoća. U uzrastu od 18 meseci, prevremeno rođena deca iz arteficijalno začetih trudnoća imaju niže postignuće na testovima za procenu psihomotornog razvoja u odnosu na prevremeno rođenu decu iz spontano začetih trudnoća. Faktori rizika koji su povezani sa lo&scaron;ijim postignućem na testu za procenu psihomotornog razvoja kod prevremeno rođene dece su arteficijalno začeće trudnoće i vi&scaron;eplodnost trudnoće. U uzrastu od 24 meseca nema razlike u telesnim parametrima između prevremeno rođene dece koja su arteficijalno začeta i prevremeno rođene dece koja su začeta prirodnim putem. U uzrastu od 24 meseca nema razlike u postignuću na testu za procenu psihomotornog razvoja kod prevremeno rođene dece su arteficijalno začeće trudnoće i vi&scaron;eplodnost trudnoće. U uzrastu od 24 meseca, prevremeno rođena deca, i iz arteficijalno, i iz spontano začetih trudnoća, na testu za procenu psihomotornog razvoja postižu rezultate koji su u skladu sa njihovim kalendarskim uzrastom.</p> / <p>Introduction: Infertility is defined as an unsuccessful conception after one year of sexual intercourse without the use of contraception in the fertilizing phase of the menstrual cycle. Assisted reproduction methods represent an effective way of treating infertility. Examination and identification of short-term and long-term effects of artificial reproductive technologies is a very challenging task. The primary reason for this is the great heterogeneity in the way of collecting, processing, classifying and interpreting, now, the abundance of information that has been gathered in various studies. Individual approach to the treatment of infertility, rapid progress and constant changes in the methodology of the artificial reproductive technologies, in addition to the aforementioned difficulties associated with the collection and analysis of data, significantly hamper accurate assessment of all possible risks and consequences artificial conception. Despite numerous studies, scientific publications and the accumulated evidence, many doubts about the question whether artificially conceived pregnancies are accompanied by the higher risks or inadequate fetal development, poor perinatal and long-term outcomes still remained.<br />The Aim: The objectives of this work were to determine the structure of morbidity in prematurely born children conceived by artificial reproductive technologies (from single and multiple pregnancies) in the first two years of life, and to identify perinatal factors that are associated with the occurrence of acute and chronic complications and diseases in prematurely born children from this pregnancies. In addition, the aim of the study was to determine the characteristics of psychomotor development in prematurely born children conceived by artificial reproductive technologies at the end of the twelfth, eighteenth and twenty-fourth month of life, as well as to identify specific risk factors for the unfavorable physical, neurological and psychological outcome of those children.<br />Materials and Methods: The study included premature born newborns who were hospitalized in the Department for neonatology and intensive and semi-intensive care unit, and are thereafter, during the first two years of life. The retrospective part of the study included children who were hospitalized at the Institute, and who were born from January 1st 2011. to December 31st 2012. and were followed up to 2 years of life. Data on patients included in the retrospective part of the survey were collected through a review of medical records. The prospective part of the study included children who were treated and followed up at the Institute, and who were born between January 1st 2013 and December 31st 2014. and then followed up to 2 years of life. From this cohort two groups were formed: The tested group (Group 1) included all preterm infants who were conceived by ART. The control group (Group 2) included naturally conceived prematurely born children. The children in the control group were selected from the cohort so that their number was equal to the number of children in the study group. The gestational age of the examinees from the control group does not differ for more than &plusmn; 4 days from the children from the study group. The date of birth of subjects included in the control group does not differ for more than &plusmn; 3 months from the children in the study group.<br />At the moment of inclusion in the study, the following individual data were taken:<br />Maternal data, pregnancy and childbirth: the age of the mother at the moment of conception, the number of previous attempts at assisted conception, professional care, place of residence, chronic diseases diagnosed before pregnancy, acute and chronic diseases diagnosed during pregnancy (hypertension, pre-eclampsia, eclampsia, liver damage), premature rupture of the fetuses, the use of medication during pregnancy, single or multiple pregnancy. Data on placental disorders and abnormalities: ablation, placenta overdose, horioamnionitis. Child-related data: intrauterine infection, intrauterine growth restriction, delivery method, Apgar score. Anthropometric parameters (body weight, body length, head circumference) at birth and during the period of outpatient monitoring of the child. Length of initial hospitalization of the child. Length of invasive and / or non-invasive respiratory support and oxygen therapy. Diagnosis on discharge from the hospital: the presence of severe consequences of prematurity, which implies intracranial hemorrhage of 3rd and 4th degree (defined in International Classification of Disease - Tenth Revision (MKB10) under code P52.2), cystic periventricular leukomalacia, retinopathy of prematurity, bronchopulmonary dysplasia , necrotizing enterocolitis, sepsis and / or meningitis (microbiologically or clinically diagnosed). Presence of congenital anomalies or genetic syndromes and diseases (defined in MKB10 under codes Q00 to Q99), as well as the presence of congenital metabolic diseases (defined in MKB10 under codes E00 to E90).<br />In the retrospective part of the study, specialist reports from a neonatological clinic were examined for child visits at the age of 12, 18 and 24 months, and the following data were ecorded: all pre-diagnosis reported on specialist reports from a neonatological clinic, anthropometric arms at the moment examination (body length, body weight and head circumference), neurological findings (tone, trophic, skin and tendon reflexes, presence of lateralization in neurological findings), ophthalmologist findings (neat / patial findings), assessment of fine and coarse motoring, speech, cognitive functions and social contact and a collective assessment of psychomotor development. In the prospective part of the study, during control examinations in a neonatological clinic, at the age of 12, 18 and 24 months, the following were determined and recorded: previously set out in the current medical documentation, anthropometric parameters at the moment of examination (body length, body weight and the volume of the head), neurological findings (tone, trophic, skin and tendon reflexes, presence of lateralization in neurological findings), ophthalmologist findings, assessment of fine and grose motor functions, speech, cognitive functions, social contact and psychomotor development.<br />Results: The average BW of subjects in Group 1 at the age of 12 months, was statistically significantly lower in relation to respondents from Group 2 (Student&#39;s T test). The average length of subjects from both groups at the age of 12 months did not statistically differ (Student&#39;s T test). The average head circumference between children from both groups, at the age of 12 months, did not statistically differ (Student&#39;s T test). The proportion of subjects with pathological ophthalmological findings did not statistically significantly differ between Group 1 and Group 2 (Fischer&#39;s exact probability test). The proportion of subjects with pathological neurological findings did not statistically significantly differ between Group 1 and Group 2 (Hi square test). The average values of the global development coefficient (RQ), as well as the average score values for individual elements of development evaluation test - Brunet-L&eacute;zine scale (motor function, coordination, speech and sociability) did not differ significantly between groups (Student t test). In Group 1 there were 92 (59.740%) of children whose uncorrected RQ was under 90, while in Group 2 there were 61 (39.610%) children whose uncorrected RQ was below 90. This difference in the number of children with RQ below the average for calendar age is statistically significant (Hi square test, p = 0.0004). The relative risk of under-achievement in the psychomotor evaluation test (RQ &lt;90) for children from Group 1 was higher than in children from Group 2 (RR = 1.495; 95% CI 1.181 - 1.922). In Group 1, there were 87 (56.494%) children who achieved sub-optimal corrected score values for the assessment of psychomotor development (corrected RQ &lt;90). In Group 2, there were 69 (44.805%) children who achieved sub-optimal corrected score values for the assessment of psychomotor development (corrected RQ &lt;90). This difference is statistically significant (Hi square test, p = 0.040). The relative risk for the suboptimal achievement in the psychomotor evaluation test (corrected RQ &lt;90) for children from Group 1 was higher than in Group 2 (RR = 1.261; 95% CI 1.008 - 1.577). In Group 1, as many as 81/87 (93.310%) of children had a corrected RQ value of &ge; 85, while in Group 2 this value of the corrected RQ there were 60/69 (86.956%) children.<br />At the age of 18 months, the average BW of subjects from both groups did not differ significantly (Student&#39;s T test). The average length of subjects from both groups, at the age of 18 months, did not statistically differ (Student&#39;s T test). The average head circumference of children from both groups, at the age of 18 months, did not statistically differ (Student&#39;s T test). The proportion of subjects with pathological ophthalmological findings did not statistically significantly differ between Group 1 and Group 2 (Hi square test). The proportion of subjects with pathological neurological findings did not statistically differ between Group 1 and Group 2 (Hi square test). The average RQ values, as well as the average scores for individual elements of psychomotor development (motor function, coordination, speech and sociability) according to the Brunet-L&eacute;zine scale, have been statistically significantly different between groups, at the age of 18 months (Student&#39;s T test). In Group 1 there were 57 (37.013%) children whose uncorrected RQ was below 90, while in Group 2 there were 31 (20,130%) children whose uncorrected RQ was below 90. The share of children with RQ below the average value for the calendar age is statistically significantly different between groups (Hi square test, p = 0.010). The relative risk for the suboptimal achievement in the Psychomotor Development Assessment (uncorrected RQ &lt;90) for Group 1 children was higher than in Group 2 (RR = 1.288; 95% CI 1.181 - 2.730). A statistically significant difference between Group 1 and Group 2 existed when the number of children with corrected RQ below 90 was compared (36 naspram 19 respectively, Hi quadrate test, p = 0.011). The relative risk for the suboptimal achievement on the Psychomotor Evaluation Test (corrected RQ &lt;90) for the children from Group 1 was higher when compared to children in Group 2 (RR = 1.895; 95% CI 1.139 &ndash; 3.152).<br />At the age of 24 months the average BW, body length and head circumference of subjects in both groups were not significantly different (Student&#39;s T test). The proportion of subjects with pathological ophthalmological findings did not statistically significantly differ between Group 1 and Group 2 (Hi square test). The proportion of subjects with pathological neurological findings did not statistically significantly differ between Group 1 and Group 2 (Hi square test). The average RQ values, as well as the average score values for individual elements for development evaluation (motor function, coordination, speech and sociability) according Brunet-L&eacute;zine scale, did not significantly differ between groups at the age of 24 months (Student&#39;s T test). In Group 1, there were 21 children (13.636%) whose uncorrected RQ was under 90, while in Group 2 there were 17 (11.049%) of children whose uncorrected RQ was below 90. The difference in the number of children with RQ below the average for the calendar age was not statistically significant (Hi square test, p = 0.488). A statistically significant difference did not exist even when the number of children with values of the corrected RQ below 90 in Group 1 and Group 2 (12 naspram 9 respectively, Hi quadrate test, p = 0.497) was compared.<br />Logistic regression analysis has shown that artificial conception, multiple pregnancy and IUGR are independent risk factors for lesser BW in a calendar age of 12 months. By logistic regression analysis, a statistically significant correlation between RQ values at 18 months of age and the following independent variables was obtained: artificially started pregnancy and multiple pregnancy. Group 1 and Group 2 patients did not significantly differ by any of the indicators of physical and psychomotor development at the age of 24 months.<br />The structure of morbidity in children, during the two-year follow-up period, did not differ significantly between groups. The only difference between the groups was found in the rates of acute respiratory infections at the age of 12 and 18 months (rate of infections was higher in Group 1), whose occurrence, however, was directly related to multiple pregnancies, or the number of sibling in the household.<br />Conclusion: The average age of mothers of children conceived by the IVF is higher than the average age of mothers of children who were conceived spontaneously. The structure of the morbidity of mothers of children who were artificially conceived and mothers of children born after spontaneous conception is the same, but the morbidity rate is higher in the mothers of children who were conceived by IVF. Pregnancies concieved by IVF almost exclusively ended by cesarean section. Premature rupture of the membranes is a common complication of IVF pregnancies. The rate of morbidity of prematurely born children conceived by ART is not higher than that of prematurely born children conceived naturally. The structure of morbidity in children from ART pregnancies was the same as in naturally conceived prematurely born children. The incidence of specific illnesses is the same, with the exception of bronchopulmonary dysplasia that occurs more frequently in children born from ART pregnancies, and retinopathy of prematurity that occurs more frequently in spontaneously conceived children. Maternal birth weight, intrauterine growth restriction, mother&#39;s age, maternal care, previous mother&#39;s chronic illness, mother&#39;s disease diagnosed during pregnancy, single and multiple pregnancies and PROM are potential risk factors for worse postnatal outcome in children from artificially initiated pregnancies. Risk factors for lower body weight in premature babies, at the age of 12 months, are: artificial conception, multiple pregnancy and intrauterine growth restriction. At the age of 12 months, prematurely born children from IVF pregnancies, have slightly worse (but not significantly lower) psychomotor achievements. At the age of 18 months, there is no difference in the indicators of physical development between prematurely born children who are artificially conceived and children born from spontaneous pregnancies. At the age of 18 months, prematurely born children from ART pregnancies have lower achievement on tests for assessing psychomotor development compared to prematurely born children from spontaneously initiated pregnancies. Risk factors associated with a poor performance on the psychomotor development assessment tests, in preterm infants, are an artificial conception of pregnancy and a multi fertile pregnancy. At the age of 24 months, there is no difference in the physical parameters between prematurely born children from ART and naturally conceived pregnancies. At the age of 24 months, there is no difference in the achievement on the test for the assessment of psychomotor development between children from ART and spontaneous pregnancies. At the age of 24 months, on the psychomotor development assessment, prematurely born children achieve the results consistent with their calendar age.</p>

Diss. (sammanfattning) Umeå : Umeå universitet, 2009. / Härtill 4 uppsatser. Även tryckt utgåva.

Thesis (MNutr (Interdisciplinary Health Sciences. Human Nutrition))--Stellenbosch University, 2008. / Objective: Primary: To investigate the effect of pasteurisation on the composition of expressed breast milk from HIV positive mothers and its adequacy in relation to the growth of their VLBW premature infants. Methods: A descriptive, prospective case-controlled pilot study was performed in 3 regional state hospitals in the Western Cape, South Africa. The control and study groups consisted of 12 HIV negative and 11 HIV positive mothers, with their VLBW premature infants, respectively. All mothers (19 - 35 years old) belonged to the Xhosa ethnic group. All infants were born <34 weeks gestation and birth weight <1500g. Eight breast milk samples were collected on days 6, 7, 13, 14, 20, 21, 27 and 28 from all mothers during the first 28 days after birth. Breast milk was expressed by hand or pump from either the right or left breast. Half of each breast milk sample was kept raw. The remaining sample was Pretoria pasteurised, after which both samples were subdivided into 3 or 4 aliquots to determine energy, protein, carbohydrate, fat, folate, calcium, phosphorus, magnesium, sodium, otassium, iron, copper, zinc content and HI viral load (study group only). The mothers’ dietary intake during pregnancy and lactation was obtained by means of a quantitative food frequency questionnaire and repeated 24-hour recall respectively. The infants’ dietary intake was recorded daily. Mothers’ anthropometric measurements taken at study entry and exit were weight, height and mid-upper arm circumference. All infants’ daily weight, as well as length and head circumference at birth and on day 28 postpartum was obtained. Biochemical analysis was performed on the blood samples obtained at study entry and exit from all mothers and infants. For statistical analysis, Statistica® (release no 7, 2006) was used for repeated measures analysis of variance (ANOVA) to determine the effect of HIV, pasteurisation, milk expression and time on the composition of the breast milk. Results: There was no significant difference in the studied macro- and micronutrient composition between raw or pasteurised expressed breast milk from HIV positive and HIV negative mothers with premature infants. A significant decline in breast milk protein (p<0.01), magnesium (p=0.045), potassium (p=0.002), zinc (p<0.01) and copper (p=0.03) content was observed for the whole study population over time, while folic acid content increased significantly (p=0.012) over time. The sodium/potassium ratio of both groups remained strongly indicative of the presence of sub-clinical mastitis. A significant (p=0.03) greater mean volume of milk was obtained with pump [42.5 Standard Deviation (SD) 18.1 ml], compared to hand expression [36.7 (16.7) ml]. Method of expression did not result in a significant difference in breast milk composition for any of the nutrients studied. Eight (35%) infants were born SGA while 21 (91%) infants were SGA on day 28. The infants gained a mean of 16.37 (4.5) g/kg/day (i.e. 91% of the recommended growth rate of >18g/kg/day) from the day on which birth weight was regained. The control and study group infants respectively consumed a mean of 3.27 (1.36) and 3.21 (1.36) g protein/kg/day and 138.1 (33.8) and 142.3 (33.8) kcal total energy/kg/day. This corresponds to a PER of 2.6 (control group) and 2.5 (study group) respectively, which cannot provide for the increased growth needs of the SGA infant in need of catch-up growth. Six infants experienced an incident of Grade 1 NEC which resolved and all completed the study. Two (18%) HIV-exposed infants were found to be HIV positive at 28 days post delivery. Four participating infants died. No adverse event or mortality was related to the study protocol as no intervention was undertaken. Conclusion: HIV positive Xhosa mothers provide as nutritious breast milk to their VLBW premature infants as HIV negative Xhosa mothers. Maternal nutrient intake during pregnancy and lactation did not have a significant effect on the nutritional composition of breast milk, except for folate content.

Submitted by Fabiana Gonçalves Pinto (benf@ndc.uff.br) on 2015-12-08T11:39:53Z No. of bitstreams: 1 Marcia Farias de Oliveira dos Santos.pdf: 7913737 bytes, checksum: 8b7f304719cb9775d8b1e05fec5959c4 (MD5) / Made available in DSpace on 2015-12-08T11:39:53Z (GMT). No. of bitstreams: 1 Marcia Farias de Oliveira dos Santos.pdf: 7913737 bytes, checksum: 8b7f304719cb9775d8b1e05fec5959c4 (MD5) Previous issue date: 2014 / Mestrado Acadêmico em Ciências do Cuidado em Saúde / Estudo realizado para obtenção do grau de Mestre em Ciências do Cuidado em Saúde da Universidade Federal Fluminense. Objeto: os processos de medicação realizados pela equipe de enfermagem da Unidade Neonatal do Hospital Universitário Pedro Ernesto. Objetivos: Descrever os processos de preparo e administração de medicamentos, executados pela equipe de enfermagem da unidade, através da construção de fluxogramas; Analisar por meio de incidentes críticos as situações, comportamentos e consequências, positivos e negativos, identificados nos processos de preparo e administração de medicamentos, a partir do relato da equipe de enfermagem. Método: Pesquisa descritiva, qualitativa, utilizando a Técnica do Incidente Crítico (TIC). Para coleta de dados a proposta foi de realização de entrevistas individuais, semiestruturadas com profissionais de enfermagem lotados no cenário do estudo pelo menos desde março de 2012, realizando atividades de assistência direta de enfermagem, sendo esta a amostragem proposital. Foi considerada atingida a saturação dos dados com 39 entrevistas realizadas, sendo 20 com enfermeiros e 19 com técnicos de enfermagem. Para realização das entrevistas contou-se com uma auxiliar de pesquisa. O material foi gravado e posteriormente transcrito. O conteúdo das entrevistas foi lido exaustivamente e pré-analisado nos moldes da TIC tendo como base a separação, nos textos de cada entrevista, dos elementos situação, comportamento e consequência e polaridades positiva e negativa. Por escolha metodológica de unir a análise de conteúdo preconizada por Flanagan àquela descrita por Bardin, os dados foram lançados em quadros, gerando unidades de registro. A seguir foi realizado o agrupamento dos incidentes críticos positivos e negativos em subcategorias, nomeadas por palavras-chave que emergiram dos conteúdos (unidades de significância), Oito categorias foram obtidas, quatro por polaridade: time de medicação, divisão de tarefas, atividades técnicas e atuação da gerência. Leituras das normas e rotinas de medicação da Unidade serviram de base para elaboração de fluxogramas dos processos de trabalho estudados. Como conclusão do estudo foi apresentado que a fluxogramação dos processos indicou a necessidade de reavaliação na divisão de tarefas durante o processos de preparo de medicamentos e necessidade de inclusão de atividades de monitoramento do sistema de medicação. Quanto a análise dos incidentes críticos, as subcategorias de incidentes negativos com mais relatos agrupados foram as denominadas divisão de tarefas e atividades técnicas. Nessas subcategorias os relatos apontaram uma preocupação com a persistência dos erros, com questões éticas e com atividades desenvolvidas em outras fases do sistema de medicação, pontos considerados prioritários nos estudos produzidos na área. Em relação à persistência dos erros, as duas metodologias utilizadas apontam para o mesmo caminho: a necessidade de monitoramento dos eventos adversos e de adoção de estratégias que diminuam a ocorrência e persistência desses eventos. Espera-se que os resultados obtidos e o produto do trabalho possam colaborar com o contínuo desenvolvimento do processo de medicação adotado na Unidade Neonatal, com o desenvolvimento de pesquisas na Instituição e com a melhoria da assistência de enfermagem em geral, já que apresenta metodologias aplicáveis à análise de processos de trabalho em qualquer realidade de cuidado. / This is a research project for the Academic Master’s Degree in the Sciences of Health Care, of the Fluminense Federal University. Object: medication processes executed by the nursing team in the Neonatal Unit of the University Hospital Pedro Ernesto.. Objectives: To describe the process of preparing and administrating the medication, which are performed by the nursing team, byusing flowcharts created to represent this work process. To analyze the situations, behavior and consequences - both positive and negative - identified in the process, based on the reports of the professionals involved. Method: This is a descriptive, qualitative research, using the Critical Incident Technique (CIT) approach. The data was collected through individual, semi-structured, recorded interviews with nursing professionals from the University Hospital. Those workers should be part of the hospital staff at least since march 201, and be involved in activities of direct care, thus being an stratified sample.The data was saturated after interviewing 39 employees: 20 nurses e 19 nurse technicians. A research assistant helped collect the interviews. The data was recorded and later transcribed. The material was then extensively read and preanalyzed following the CIT precepts. ,by separating the following elements: situation, behavior and consequence, and its respective positive and/or negative polarities. It was decided that the methodology of this research would unite the content analysis as it was defined by Flanagan to that of Bardin; this resulted in the creating of data tables from which registration unities were extracted. Afterwards, the positive and negative critical incidents were grouped in subcategories, named after key-words noted from the content of the interviews. Eight categories were obtained, four per polarity: the medication team, task division, implanted technical activities and the actions of the management. The rules and routines of the medication unit served as the base for the elaboration of flowcharts of the studied work processes. The resulting flowchart indicated the need to reevaluate the task division in the process of preparing and administrating the medications, as well as the inclusion of monitoring activities in the medication system. The analysis of the critical incidents showed that the subcategory of negative critical incidents with the most reports were task division and implanted technical activities, in which reports indicated concerns about the persistence of errors, ethical matters and with the activities performed in other stages of the medication process; points that are consistently approached in studies in the field. In relation to error persistence, both of the methodologies applied point out to the same path: the need to monitor the adverse events, and the implementation of strategies to reduce its persistency and occurrences. The author hopes that the results obtained might assist with the continuous development of the medication system adopted by the Neonatal Unit and with the development of researches in the institution, as well as helping improve the nursing assistance in general, since this research works with a methodology which can be applied in the analyzes of work processes in any care-related context.

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