Enteral adequacy of the diet of low-birth-weight preterm newborns: A prospective cohort study.

OBJECTIVE: This study aimed to verify the dietary adequacy of full enteral feeding in preterm newborns (PTNB) and its relationship with birth weight (BW) during the period of hospitalization in the neonatal intensive care unit (NICU). METHODS: This is a prospective cohort study whose population were babies born at less than 37 gestational weeks and weighing less than 2500 g, admitted to a NICU. PTNB were monitored regarding their dietary evolution, considering parenteral and enteral nutrition and adequacy of diet supply in terms of volume, energy, and protein. For statistical analysis, the Statistical Package for the Social Sciences (SPSS) software was used, considering p < 0.05 as significant. RESULTS: A total of 76 PTNB were included. The mean time of using parenteral nutrition was 14 days. The mean time to reach the full enteral feeding for nutrition (FEF-N) was 29 days. However, half of the PTNB reached nutritional recommendations after this means. The time to achieve FEF-N was influenced by BW. Additionally, BW significantly influenced the length of stay in the NICU (p < 0.001). When reaching the recommended full enteral feeding for hydration (FEF-H), 60% of the sample was unable to reach the recommended energy and protein intake. CONCLUSIONS: BW influenced the time needed to reach the FEF-H and FEF-N. The lower the BW, the longer it took to achieve dietary adequacy. Despite achieving the FEF-H, most premature babies did not reach the necessary energy and protein intake at the appropriate time.

Impacts of Consumption of Ultra-Processed Foods on the Maternal-Child Health: A Systematic Review.

Background and Aims: Changes in eating patterns have been leading to an increase in the consumption of ultra-processed foods (UPF), negatively impacting the quality of the diet and generating risk of harm to the health of the adult population, however, there is no systematized evidence of the impact of UPF in maternal-child health. Thus, in this study we aimed to evaluated the association between UPF consumption and health outcomes in the maternal-child population. Methods: Systematic review registered on the International Prospective Register of Systematic Reviews (PROSPERO) (CRD42021236633), conducted according to the PRISMA diagram in the following databases: PubMed, Medline, Scopus, Web of Science, Scielo, and CAPES thesis and dissertation directory. We included original cross-sectional, case-control and cohort studies in any language. Eligibility criteria were (a) food consumption assessment by the NOVA classification, (b) health outcome (nutritional or diseases), and (c) maternal-child population (pregnant, lactating women and infants/children). All data were analyzed and extracted to a spreadsheet structured by two independent reviewers. We evaluated the methodological quality of the studies included using the Newcastle-Otawa Scale and RoB 2. Results: Searches retrieved 7,801 studies and 15 contemplated the eligibility criteria. Most studies included were cohort studies (n = 8, 53%), had children as their population (n = 9, 60%) and only one study evaluated UPF consumption in infants and lactating women. Panoramically, we observed that a higher participation of UPF in children's diet has been associated with different maternal-child outcomes, such as increase of weight gain, adiposity measures, overweight, early weaning, lower diet quality, metabolic alterations, diseases, and consumption of plastic originated from packaging. Only one of the studies included did not present high methodological quality. Conclusion: Despite the limited literature on UPF consumption and health outcomes in the maternal-child population, the highest UPF consumption negatively impacted nutrition and disease development indicators in pregnant, lactating women and children. Considering the expressive participation of these foods in the diet, other studies should be conducted to further investigate the impact of UPF consumption on different health indicators, especially in the lactation phase for this was the one to present the most important knowledge gap. Systematic Review Registration: [https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42021236633], identifier [CRD42021236633].

Evaluation of human milk titratable acidity before and after addition of a nutritional supplement for preterm newborns / Avaliação da acidez titulável do leite humano antes e após adição de um suplemento nutricional para recém-nascido pré-termo

Abstract Objective: To evaluate the initial Dornic acidity in raw human milk, after pasteurization and after heating and dilution of a dietary supplement for preterm infants. Methods: A quantitative, descriptive, and experimental study was carried out with a convenience sample at the human milk bank at a Brazilian public maternity, with specialized care for pregnant women and newborns at risk. The eligibility criteria for the study sample included 93 frozen raw human milk in suitable containers with volumes ≥100 mL and initial Dornic acidity ≤8° Dornic (ºD). Milk acidity of human milk was measured in four stages: in raw human milk (initial); after pasteurization; after the heating of pasteurized milk and dilution of the supplement; and after thirty minutes of supplementation. Results: The initial acidity was 3.8° D ± 1.3 (95% CI: 3.56-4.09) with no significant difference in Dornic acidity in pasteurized milk, which was 3.6° D ± 1.2 (95% CI: 3.36-3.87). The dilution of the supplement in pasteurized milk that was heated significantly increased mean Dornic acidity to 18.6 °D ± 2.2 (95% CI: 18.18-19.11), which remained high after thirty minutes of supplementation at 17.8 °D ± 2.2 (95% CI: 17.36-18.27), considering p < 0.05. Conclusions: The study observed no significant differences in Dornic acidity of raw human milk and pasteurized human milk; however, the dilution of a human milk supplementation caused a significant increase in acidity. Further investigations are necessary on the influence of this finding on the quality of supplemented milk and its consequences on the health of preterm infants.

Resumo Objetivo Avaliar a acidez Dornic inicial no leite humano cru, após pasteurização, e aquecimento e diluição de um suplemento nutricional para recém-nascidos prematuros. Métodos Estudo quantitativo, descritivo, experimental, com amostragem por conveniência, feito no Banco de Leite Humano de uma maternidade pública brasileira, com assistência especializada às gestantes e recém-nascidos de risco. Os critérios de elegibilidade das 93 amostras do estudo incluíram leites humanos crus congelados em embalagens apropriadas, com volumes ≥ 100 mL e acidez Dornic inicial ≤ 8°Dornic (°D). A acidez Dornic dos leites humanos foi mensurada em quatro momentos: no leite humano cru (inicial); após pasteurização; após aquecimento do leite pasteurizado e diluição do suplemento; e após transcorridos 30 minutos de suplementação. Resultados A acidez inicial foi de 3,8°D ± 1,3 (IC 3,56-4,09) e não apresentou diferença significativa em relação à acidez Dornic no leite pasteurizado, que foi de 3,6°D ± 1,2 (IC 3,36-3,87). A diluição do suplemento no leite pasteurizado e aquecido aumentou significativamente a média da acidez Dornic a 18,6°D ± 2,2 (IC 18,18-19,11), a qual se manteve elevada em 17,8°D ± 2,2 (IC 17,36-18,27) após 30 minutos da diluição, considerando p < 0,05. Conclusões O estudo demonstrou que a acidez Dornic do leite humano cru e a do leite humano pasteurizado não apresentaram diferenças significativas, porém a diluição do suplemento de leite humano promoveu elevação significativa da acidez. Maiores investigações da influência desse achado sobre a qualidade do leite suplementado e suas consequências na saúde de prematuros são necessárias.

Estado nutricional em vitamina A de puérperas adolescentes e adultas assistidas em maternidade pública / Vitamin A status of puerperal adolescents and adults attending public maternity hospitals

RESUMO Objetivo Avaliar o estado nutricional em vitamina A de puérperas adolescentes e adultas em relação à ingestão alimentar, retinol no soro e colostro e o suprimento desta vitamina para o recém-nascido. Métodos Estudo transversal, incluindo 136 puérperas, sendo 68 adolescentes e 68 adultas, atendidas em uma maternidade pública. A ingestão dietética de vitamina A foi estimada por um questionário de frequência do consumo alimentar. Foram coletados sangue e colostro em condição de jejum para análise dos níveis de retinol. As amostras foram analisadas por cromatografia líquida de alta eficiência. A estimativa da ingestão de vitamina A pelo recém-nascido foi calculada pelo volume ingerido de leite e a média da concentração de retinol no colostro materno. Resultados A estimativa de consumo foi 681,2±535 µgRAE/dia, para as adolescentes, e 891,8±831,5 µgRAE/dia, para as adultas (p>0,05). As médias de retinol sérico foram 40,6±9,7 µg/dL, no grupo das adolescentes, e 44,9±10,9 µg/dL, no das adultas (p<0,05). No colostro, as adolescentes apresentaram concentração de retinol de 83,1±26,5 µg/dL e as adultas de 81,8±29,8 µg/dL (p>0,05). O volume médio ingerido pelos lactentes provenientes de puérperas adolescentes foi de 435,1+140,7 µgRAE/dia e de 409,7+150,8 µgRAE/dia pelos recém-nascidos das adultas. Na análise individual, 42,6% (n=29) das adolescentes e 52,9% (n=36) das mães adultas não supriram adequadamente a recomendação diária do lactente. Conclusão As adolescentes apresentaram ingestão inadequada de vitamina A. Ambos os grupos apresentaram percentuais de inadequação no soro e colostro e, consequentemente, no fornecimento da vitamina A aos recém-nascidos.

ABSTRACT Objective To assess the vitamin A status of puerperal adolescents and adults in relation to food intake, serum and colostrum retinol, and the supply of this vitamin to the newborn. Methods Dietary vitamin A intake was investigated by a food frequency questionnaire. Fasting blood and colostrum samples were collected for retinol quantification by high-performance liquid chromatography. Newborn vitamin A intake was given by multiplying milk intake by the mean colostrum retinol level. Results This cross-sectional study included 136 puerperal women (68 adolescents and 68 adults) seen at a public maternity hospital. The estimated dietary intake was 681.2±535 µgRAE/day for adolescents and 891.8±831.5 µgRAE/day for adults (p>0.05). The mean serum retinol levels were 40.6±9.7 µg/dL in adolescents and 44.9±10.9 µg/dL in adults (p<0.05). The mean colostrum retinol levels in adolescents and adults were 83.1±26.5 µg/dL and 81.8±29.8 µg/dL, respectively (p>0.05). The adolescents' newborns had a mean retinol intake of 435.1±140.7 µgRAE/day, and the adults' newborns had a mean retinol intake of 409.7 ± 150.8 µgRAE/day. Twenty-nine (42.6%) adolescents and thirty-six (52.9%) adults did not supply enough vitamin A per day to their newborns. Conclusion Adolescents had inadequate vitamin A intake. Adolescents and adults had similar prevalences of inadequate serum retinol. Some adolescents and adults had inadequate colostrum retinol levels, resulting in low retinol intake by their newborns.

Evaluation of human milk titratable acidity before and after addition of a nutritional supplement for preterm newborns.

OBJECTIVE: To evaluate the initial Dornic acidity in raw human milk, after pasteurization and after heating and dilution of a dietary supplement for preterm infants. METHODS: A quantitative, descriptive, and experimental study was carried out with a convenience sample at the human milk bank at a Brazilian public maternity, with specialized care for pregnant women and newborns at risk. The eligibility criteria for the study sample included 93 frozen raw human milk in suitable containers with volumes ≥100mL and initial Dornic acidity ≤8° Dornic (°D). Milk acidity of human milk was measured in four stages: in raw human milk (initial); after pasteurization; after the heating of pasteurized milk and dilution of the supplement; and after thirty minutes of supplementation. RESULTS: The initial acidity was 3.8°D±1.3 (95% CI: 3.56-4.09) with no significant difference in Dornic acidity in pasteurized milk, which was 3.6°D±1.2 (95% CI: 3.36-3.87). The dilution of the supplement in pasteurized milk that was heated significantly increased mean Dornic acidity to 18.6°D±2.2 (95% CI: 18.18-19.11), which remained high after thirty minutes of supplementation at 17.8°D±2.2 (95% CI: 17.36-18.27), considering p<0.05. CONCLUSIONS: The study observed no significant differences in Dornic acidity of raw human milk and pasteurized human milk; however, the dilution of a human milk supplementation caused a significant increase in acidity. Further investigations are necessary on the influence of this finding on the quality of supplemented milk and its consequences on the health of preterm infants.