7 research outputs found
Nutritional Issues in Children with Dysphagia.
(1) Background: Pediatric dysphagia presents significant nutritional challenges, often
impacting growth and development due to reduced oral intake, increased nutritional needs, and
gastrointestinal complications; (2) Methods: This prospective quasi-experimental study assessed
117 children under 14 years old (20 patients were under 1 year old, 80 were aged 1–7 years, and 17
were older than 7 years), diagnosed with swallowing disorders, to analyze their caloric, macro-, and
micronutrient intake and identify potential deficiencies. The severity of dysphagia was established
using functional oral intake scales, and dietary records were reviewed over a 3-day period; (3) Results:
The study revealed that 39.8% of participants did not meet their total energy expenditure (TEE),
highlighting a high prevalence of malnutrition among these children. Furthermore, patients using
feeding devices exhibited a significantly lower caloric intake, and over half required significantly
modified food textures. After individualized speech therapy and nutritional rehabilitation, partici-
pants showed significant improvements in caloric intake, with their energy coverage increasing from
958% to 1198% of the daily requirement. Rehabilitation also improved tolerance to a broader range
of food textures; (4) Conclusions: This research underscores the importance of multidisciplinary,
individualized nutritional strategies to address the specific challenges of pediatric dysphagia, empha-
sizing the role of enteral nutrition and therapeutic interventions in improving the quality of life and
nutritional outcomes of these children. Further studies are recommended to assess the long-term
impact of such strategies
Herbst’s Triad as a Manifestation of Gastroesophageal Reflux Disease
The Herbst triad (HT) was described in 1976 by Herbst et al. (1) when detecting the association of iron deficiency anemia, hypoalbuminemia and clubbing in 3 children with hiatal hernia and severe esophagitis secondary to gastroesophageal reflux (GER). Although no chronic lung disease associated with reflux was demonstrated to justify the appearance of clubbing, these also disappeared after surgery (1). We present 2 children with HT that required surgical treatment due to lack of response to proton pump inhibitors
The New Molecules Are Changing the Course of Pediatric Chronically Active Ulcerative Colitis: A Series of Pediatric Cases
Chronically active ulcerative colitis (UC) constitutes a challenge in an era where medical therapeutic options have increased while experience with colectomies has decreased. The change in the therapeutic paradigm of the disease means that patients with chronically active UC are being managed waiting to find their therapeutic target. We present 2 cases of children with chronically active UC who did not respond to intravenous steroids nor sequential therapy. A response was obtained with ustekinumab and tofacitinib, 2 drugs widely used in adults but still with little evidence in children. Highlighting the important role of patients and their families helped decision-making, facilitating the work of the medical team. With multidisciplinary management and close follow-up, they have been able to avoid surgery entering complete clinical remission
Sirolimus for the Treatment of Juvenile Polyposis in Childhood
Juvenile polyposis syndrome (JPS) is a rare disease with an autosomal dominant inheritance pattern characterized by the development of multiple hamartomatous polyps in the gastrointestinal tract. The most frequent signs and symptoms are recurrent abdominal pain, rectal bleeding, anemia, and iron deficiency. The treatment of JPS is symptomatic, requiring serial endoscopic polypectomies or intestinal resections in the most severe cases. We describe the clinical case of a patient with JPS with a childhood juvenile polyposis phenotype because of a mutation on the SMAD4 gene, who received treatment with sirolimus successfully
Nutritional Issues in Children with Dysphagia
(1) Background: Pediatric dysphagia presents significant nutritional challenges, often impacting growth and development due to reduced oral intake, increased nutritional needs, and gastrointestinal complications; (2) Methods: This prospective quasi-experimental study assessed 117 children under 14 years old (20 patients were under 1 year old, 80 were aged 1–7 years, and 17 were older than 7 years), diagnosed with swallowing disorders, to analyze their caloric, macro-, and micronutrient intake and identify potential deficiencies. The severity of dysphagia was established using functional oral intake scales, and dietary records were reviewed over a 3-day period; (3) Results: The study revealed that 39.8% of participants did not meet their total energy expenditure (TEE), highlighting a high prevalence of malnutrition among these children. Furthermore, patients using feeding devices exhibited a significantly lower caloric intake, and over half required significantly modified food textures. After individualized speech therapy and nutritional rehabilitation, participants showed significant improvements in caloric intake, with their energy coverage increasing from 958% to 1198% of the daily requirement. Rehabilitation also improved tolerance to a broader range of food textures; (4) Conclusions: This research underscores the importance of multidisciplinary, individualized nutritional strategies to address the specific challenges of pediatric dysphagia, emphasizing the role of enteral nutrition and therapeutic interventions in improving the quality of life and nutritional outcomes of these children. Further studies are recommended to assess the long-term impact of such strategies