Instituto da Criança - HC/ICr

O Instituto da Criança (ICr) é parte do Sistema Faculdade de Medicina da Universidade de São Paulo - Hospital das Clínicas (FMUSP-HC), atende a pacientes de 0 a 19 anos de todo o Brasil e da América Latina em 21 especialidades médicas, incluindo assistência ambulatorial, internação clínica e cirúrgica. Inaugurado em 1976, o hospital foi preparado para atender doenças de alta complexidade como síndromes raras, Câncer, AIDS, além de realizar transplantes de fígado e de medula óssea.

O ICr possui o Serviço de Diagnóstico por Imagem (SDI) e dispensa atenção especial às necessidades da criança e do adolescente, integrando a estrutura biológica, psicológica e social de cada paciente. O atendimento é realizado por equipes multiprofissionais compostas por assistentes sociais, educadores, enfermeiros, fisioterapeutas, médicos, nutricionistas, psicólogos e terapeutas ocupacionais. Essa atuação conjunta torna o atendimento completo e eficaz, num ambiente que remete ao mundo infantil, utilizando brincadeiras, desenhos, cores e muita diversão. Os profissionais do ICr são orientados pelos pilares fundamentais de um hospital-escola: Assistência, Ensino, Pesquisa e contam com o apoio do Departamento de Pediatria da FMUSP.

Site oficial: http://www.icr.usp.br/

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Recent Submissions

  1. Exploring the Brazilian pediatric palliative care network: a quantitative analysis of a survey data

    REVISTA PAULISTA DE PEDIATRIA, v.41, 2023

    Objective: The aim of this study was to identify the characteristics of services in Brazil that compound the Brazilian Pediatric Palliative Care (PPC) Network. Methods: An online survey was conducted among representatives from PPC services. A total of 90 services from Brazil completed the online ...

  2. <i>POLR1A</i> variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies

    AMERICAN JOURNAL OF HUMAN GENETICS, v.110, n.5, p.809-825, 2023

    Heterozygous pathogenic variants in POLR1A, which encodes the largest subunit of RNA Polymerase I, were previously identified as the cause of acrofacial dysostosis, Cincinnati-type. The predominant phenotypes observed in the cohort of 3 individuals were craniofacial anomalies reminiscent of Treac...

  3. Small and large bowel anatomy is associated with enteral autonomy in infants with short bowel syndrome: A retrospective cohort study

    JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, v.48, n.2, p.231-238, 2024

    Background: Achievement of enteral autonomy (EA) is the ultimate treatment goal in pediatric intestinal failure (IF). We aimed to assess predictors of EA in pediatric short bowel syndrome (SBS) and explore the impact of residual small bowel (SB) and large bowel (LB) length on EA.Methods: A retros...

  4. Effect of manual hyperinflation with versus without positive end-expiratory pressure on dynamic compliance in pediatric patients following congenital heart surgery: A randomized controlled trial

    MEDICINE, v.102, n.43, article ID e35715, 8p, 2023

    Background: We aimed to compare the effect of manual hyperinflation with versus without positive end-expiratory pressure (PEEP) on dynamic compliance of the respiratory system in pediatric patients undergoing congenital heart surgery; to assess the safety of the technique in this population.Metho...

  5. Malnutrition and Nutrition Support in Latin American PICUs: The Nutrition in PICU (NutriPIC) Study

    PEDIATRIC CRITICAL CARE MEDICINE, v.24, n.12, p.1033-1042, 2023

    OBJECTIVES: To characterize the nutritional status of children admitted to Latin American (LA) PICUs and to describe the adequacy of nutrition support in reference to contemporary international recommendations. DESIGN: The Nutrition in PICU (NutriPIC) study was a combined point-prevalence study o...

  6. Real-world data of Brazilian adults with X-linked hypophosphatemia (XLH) treated with burosumab and comparison with other worldwide cohorts

    MOLECULAR GENETICS & GENOMIC MEDICINE, v.12, n.2, article ID e2387, 27p, 2024

    Background: Disease-related variants in PHEX cause XLH by an increase of fibroblast growth factor 23 (FGF23) circulating levels, resulting in hypophosphatemia and 1,25(OH)(2) vitamin D deficiency. XLH manifests in early life with rickets and persists in adulthood with osseous and extraosseous man...

  7. Physician Perceptions of and Barriers to Pediatric Palliative Care for Children With Cancer in Brazil

    JCO GLOBAL ONCOLOGY, v.9, article ID e2300057, 10p, 2023

    PURPOSE Early integration of pediatric palliative care (PPC) for children with cancer is critical to improving the quality of life of both the patient and family. Understanding physician perceptions of palliative care and perceived barriers to early integration is necessary to develop PPC in Braz...

  8. Body composition in pediatric patients

    NUTRITION IN CLINICAL PRACTICE, v.38, suppl.2, p.S84-S102, 2023

    Undernutrition is highly prevalent in children who are critically ill and is associated with increased morbidity and mortality, including a higher risk of infection due to transitory immunological disorders, inadequate wound healing, reduced gut function, longer dependency on mechanical ventilati...

  9. Data-driven, cross-disciplinary collaboration: lessons learned at the largest academic health center in Latin America during the COVID-19 pandemic

    FRONTIERS IN PUBLIC HEALTH, v.12, article ID 1369129, 15p, 2024

    Introduction The COVID-19 pandemic has prompted global research efforts to reduce infection impact, highlighting the potential of cross-disciplinary collaboration to enhance research quality and efficiency.Methods At the FMUSP-HC academic health system, we implemented innovative flow management r...

  10. Glioneuronal and Neuronal Tumors: Who? When? Where? An Update Based on the 2021 World Health Organization Classification

    NEUROGRAPHICS, v.13, n.1, 2023

    Neuronal and glioneuronal tumors usually have a benign course and may have typical imaging characteristics, allowing their diagnosis based on MR imaging findings. The most common lesions are dysembryoplastic neuroepithelial tumors and gangliogliomas, which have typical imaging characteristics. Th...