1,543 results match your criteria: "Hospital Materno-Infantil[Affiliation]"

Background: Cystic fibrosis (CF) is an autosomal recessive, chronic, potentially lethal genetic disease. CF manifestations are due to mutations in the CF transmembrane receptor transporter (CFTR) gene which codes for a protein (CFTR) that acts as an anion transporter, mainly chlorine, at epithelial cells where it is expressed. Cystic fibrosis related liver disease (CFRLD) includes a spectrum of hepatobiliary manifestations whose diagnosis and follow-up remains a challenge.

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The increase in the global prevalence of type 2 diabetes mellitus (DM2), driven mainly by obesity and physical inactivity, has increased interest in various nonpharmacological therapies. This systematic review aims to establish the effectiveness of high-intensity interval training (HIIT) and resistance exercise (RE) compared with continuous aerobic exercise in improving control in patients with DM2. We conducted a comprehensive search for clinical trials using databases such as MEDLINE (PubMed) and Web of Science.

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Hypertensive disorders of pregnancy represent an escalating global health concern with increasing incidence in low- to middle-income countries and high-income countries alike. The current lack of methods to detect the subclinical stages of preeclampsia (PE) and fetal growth restriction (FGR), two common vascular disorders of pregnancy, limits treatment options to minimize acute- and long-term adverse outcomes for both mother and child. To determine whether impaired maternal cardiovascular or uteroplacental vascular function precedes the onset of PE and/or FGR (PE-FGR), we used non-invasive techniques to obtain serial measurements of maternal cardiac output (CO), stroke volume (SV), systemic vascular resistance (SVR), as well as uterine and fetal arterial resistance at gestational weeks 10-16, 20-24 and 30-34 for 79 maternal-infant pairs in La Paz-El Alto, Bolivia (3850 m), where the chronic hypoxia of high altitude increases the incidence of PE and FGR.

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Objective: To explore the association of maternal characteristics, oxygenation, and mechanical ventilatory parameters with fetal and neonatal outcomes.

Methods: The present study was a multicenter, binational (Argentina/Colombia), prospective, cohort study, conducted in 21 intensive care units (ICUs) and including pregnant or postpartum patients with COVID-19 pneumonia requiring advanced respiratory support and their fetuses/neonates. Advanced respiratory support was defined as high-flow nasal cannula (HFNC), non-invasive ventilation (NIV) or invasive mechanical ventilation (IMV).

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Objective: To examine the relationship between etiologically-based preterm birth sub-groups and early postnatal growth according to gestational age at birth.

Methods: Prospective, multinational, cohort study involving 15 hospitals that monitored preterm newborns to hospital discharge. Measures/exposures: maternal demographics; etiologically-based preterm birth sub-groups; very, moderate and late preterm categories, and feeding.

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Article Synopsis
  • - The study investigates listeriosis, a disease caused by a Gram-positive bacterium, particularly focusing on its impact on pregnant women, who have a higher risk of severe outcomes, with symptoms like fever and abdominal pain being common.
  • - A retrospective analysis of six confirmed listeriosis cases at Hospital Materno Infantil de Málaga revealed complications such as intrauterine death, but antibiotic treatment showed positive results.
  • - The findings highlight the importance of early diagnosis and treatment to enhance outcomes for both mothers and their babies, as untreated listeriosis can lead to severe fetal complications, including prematurity and infections.
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A ten-year experience with the diagnosis of von Willebrand disease in Mexico based on a cost-effective strategy.

Arch Med Res

November 2024

Unidad de Investigacion Médica en Trombosis, Hemostasia y Aterogénesis, Instituto Mexicano del Seguro Social, Mexico City, Mexico. Electronic address:

Background: Von Willebrand disease (VWD), is the most common inherited bleeding disorder worldwide, but its diagnosis is complicated, expensive, and poorly evaluated in several countries.

Objective: To report our long-term experience with the diagnosis of VWD based on a cost-effective strategy.

Methods: We studied 802 Mexican patients, men and women, children, and adults, with clinical suspicion of VWD.

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Direct medical costs of polyarthritis in a pediatric hospital in Mexico.

Bol Med Hosp Infant Mex

November 2024

Unidad de Investigación en Epidemiología y Servicios de Salud, Área de Envejecimiento, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.

Article Synopsis
  • Juvenile idiopathic arthritis (JIA) is a common childhood illness, with the polyarticular type affecting 63-66% of patients, and this study focused on its direct medical costs in a Mexican hospital.
  • Analyzed records from January to September 2022 revealed that the average medical cost for a patient over the first 10 years of treatment was approximately $4,555, with medications constituting 82.7% of these costs, primarily from biological disease-modifying drugs (bDMARDs).
  • The study concluded that the high cost of bDMARDs significantly impacts treatment expenses and suggested exploring generic options and negotiating prices to reduce overall costs for health institutions in Mexico.
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Background: Langerhans cell histiocytosis (LCH) is a rare neoplastic disease characterized by clonal proliferation of den-dritic cells. It is Mexico's ninth most frequent malignancy in patients under 18 years of age. The aim of the study was to determine the clinical characteristics, treatment, and survival of Mexican pediatric patients diagnosed with LCH treated from January 2010 to December 2018.

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Introduction: patients with congenital heart disease are considered to be at high nutritional risk due to alterations in the metabolism of the underlying pathology and extracardiac factors. The STAMP (Screening Tool for the Assessment of Malnutrition in Paediatrics) is the only tool validated in our country in a pediatric population for nutritional screening.

Objective: to evaluate nutritional risk by STAMP screening in pediatric patients according to type of congenital heart disease.

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Article Synopsis
  • Fanconi anemia (FA) is a rare genetic disorder marked by varying symptoms and significant chromosome fragility, leading to severe health issues like cancer and bone marrow failure.
  • The Spanish Registry of Patients with FA gathered data from 227 patients over 30 years, revealing an 86% cumulative cancer incidence by age 50, with outcomes differing based on chromosome fragility and specific gene mutations.
  • Findings suggest that patients with mutations allowing some protein function (genetic hypomorphism) tend to have better health outcomes, indicating potential for new therapies that could enhance mutant FA protein function to improve patient prognosis.
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Objective: To understand the routine and implications on the mental health of hospitalized children with cancer, from the perspective of family members.

Method: Qualitative research, carried out with 11 relatives of children hospitalized in an oncopediatric inpatient unit, during the month of September 2022. The information was produced through semi-structured interviews and was analyzed according to Minayo's Thematic Analysis, emerging two categories: "The child's routine during hospitalization" and "The child's mental health during hospitalization".

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Short interbirth interval and adverse pregnancy outcomes: a Bayesian network approach.

AJOG Glob Rep

November 2024

Laboratorio de Epidemiología Genética, Centro de Educación Médica e Investigaciones Clínicas-Consejo Nacional de Investigaciones Científicas y Técnicas (CEMIC-CONICET), Ciudad Autónoma de Buenos Aires, Argentina (Campaña, López Camelo, Rittler).

Article Synopsis
  • Short interbirth interval (IBI) has been linked to negative perinatal outcomes, with this study focusing on its effects in a large South American population.
  • The research found that young mothers (≤19 years) were at a higher risk for short IBI, while older mothers (≥30 years) had a lower risk, often influenced by prior abortions.
  • Results showed that short IBI was significantly associated only with low birth weight (LBW) and had indirect relationships with preterm birth (PTB) and gastroschisis, highlighting the importance of maternal age and previous pregnancy history in these outcomes.*
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Background: Lymphatic disorders such as protein-losing enteropathy, plastic bronchitis, and chylothorax are important complications of the Fontan circulation and ultimately result in an increased risk of early death. Several European centers are now performing lymphatic procedures. The aim of this study is to map the extent of these lymphatic disorders and treatments provided across European pediatric cardiology centers.

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Background: Although genetic variants in are the most frequent cause of pediatric genetic dilated cardiomyopathy (DCM), there are no studies available describing this entity. We sought to describe clinical features, analyze variant location, and explore predictors of bad prognosis in pediatric -related DCM.

Methods And Results: We evaluated clinical records from 44 patients (24 men; median age at diagnosis, 0.

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Article Synopsis
  • - The Brazilian Rare Diseases Network (RARAS) was established in 2020 to conduct a nationwide epidemiological survey on rare diseases (RDs) in Brazil, addressing the lack of comprehensive national data since the Comprehensive Care Policy for RDs began in 2014.
  • - A total of 12,530 patients were surveyed, with a median age of 15 years; significant findings included that 63.2% had confirmed diagnoses, primarily of phenylketonuria, cystic fibrosis, and acromegaly, and average diagnostic delays lasting 5.4 years.
  • - The majority of diagnoses and treatments were funded by the Public Health System, with notable rates of hospitalization (44.5%) and a mortality rate
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There are limitations to predicting perinatal asphyxia, as current tools rely almost entirely on fetal cardiotocography (CTG). The fetal lack of responsiveness scale (FLORS) is a new diagnostic alternative based on the physiological phenomena associated with fetal hypoxia. The objective of this study was to develop, validate, and assess the diagnostic accuracy of the FLORS for predicting severe perinatal hypoxia (SPH).

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Torque teno virus: a potential marker of immune reconstitution in youths with vertically acquired HIV.

Sci Rep

October 2024

Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.

Torque teno virus (TTV) viral load (VL), a component of the human virome, increases during immune suppression or dysregulation. This study aimed to explore TTV VL in youths living with vertically acquired HIV (YWVH) and its potential as an immunovirological marker. We performed an observational, retrospective study involving YWVH under antiretroviral treatment (ART) from the Spanish Cohort of HIV-infected children, adolescents, and vertically HIV-infected patients transferred to Adult Units (CoRISpe-FARO), compared to HIV-negative healthy donors (HD).

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Gestational weight gain and daily life impact of pregnancy symptoms in healthy women: A multivariable analysis.

Eur J Obstet Gynecol Reprod Biol

December 2024

Department of Preventive Medicine and Public Health Faculty of Medicine, University of Granada, Granada, Spain; CIBER Epidemiología y Salud Pública (CIBERESP), Instituto de Salud Carlos III (ISCIII), Madrid, Spain; Instituto de Investigación Biosanitaria de Granada (ibs.GRANADA), Granada, Spain. Electronic address:

Objective: To study the relationship between gestational weight gain (GWG) and Daily Life Impact of Pregnancy Symptoms (DLIPS) scores.

Methods: A multivariable analysis of a clinical trial (the Walking Preg_Project (WPP), ClinicalTrials.gov NCT03735381) was conducted.

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Article Synopsis
  • Lung ultrasound could be a valuable tool in predicting the severity of lung disease and the need for extended ventilatory support in critically ill children.
  • In a study involving 538 children in the ICU, those requiring prolonged mechanical ventilation (over 7 days) had significantly higher lung ultrasound scores at 12 and 48-72 hours post-admission.
  • The lung ultrasound score demonstrated a strong correlation with oxygen levels and was effective in predicting prolonged mechanical ventilation, showing high accuracy in both initial assessment and multivariable analysis.
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Eculizumab as first-line treatment for patients with severe presentation of complement factor H antibody-mediated hemolytic uremic syndrome.

Pediatr Nephrol

October 2024

Laboratorio de Hemostasia y Trombosis, Instituto de Medicina Experimental-CONICET Academia, Nacional de Medicina, Buenos Aires, Argentina.

Article Synopsis
  • The study focuses on treating four children with FH antibody-mediated hemolytic uremic syndrome (HUS) using eculizumab, an alternative therapy, alongside immunosuppression instead of traditional treatments like plasmapheresis.
  • In the review, patients displayed improvements in hematological signs and kidney function within weeks of starting eculizumab, with three of them discontinuing the treatment after six months without complications.
  • The findings indicate that a short eculizumab regimen could effectively reverse severe symptoms and enhance kidney health, potentially with lower relapse risks when combined with immunosuppressive agents.
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Article Synopsis
  • Venous thromboembolic disease (VTE) includes deep vein thrombosis (DVT) and pulmonary embolism (PE), posing significant health risks globally due to its potential for recurrence and serious consequences.
  • A study conducted in Sincelejo, Colombia, reviewed 126 medical records to identify risk factors for unprovoked PE, revealing that higher levels of coagulation factor VIII and an A1-positive phenotype are significant predictors of this condition.
  • Results suggest implementing preventive strategies to mitigate the incidence and recurrence of PE, particularly in patients with identified risk factors.
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Article Synopsis
  • The study aimed to assess disease activity, muscle strength, and functional abilities in newly diagnosed juvenile dermatomyositis (JDM) patients over a 2-year period.
  • A total of 96 JDM patients were evaluated at diagnosis and at 6, 12, 18, and 24 months using various clinical assessment tools, showing significant improvements in some areas, particularly in the first 6 months.
  • Despite overall improvement in disease activity scores, some measures like childhood myositis and disability indices showed no significant progress, indicating ongoing functional impairment.
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