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2.
J Pediatr Gastroenterol Nutr ; 76(4): 533-546, 2023 04 01.
Article in English | MEDLINE | ID: mdl-36720091

ABSTRACT

Children with Hirschsprung disease have postoperative long-term sequelae in defecation that contribute to morbidity and mortality and significantly impact their quality of life. Pediatric patients experience ongoing long-term defecation concerns, which can include fecal incontinence (FI) and postoperative obstructive symptoms, such as constipation and Hirschsprung-associated enterocolitis. The American Pediatric Surgical Association has developed guidelines for management of these postoperative obstructive symptoms and FI. However, the evaluation and management of patients with postoperative defecation problems varies among different pediatric gastroenterology centers. This position paper from the Neurogastroenterology & Motility Committee of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition reviews the current evidence and provides suggestions for the evaluation and management of postoperative patients with Hirschsprung disease who present with persistent defecation problems.


Subject(s)
Fecal Incontinence , Gastroenterology , Hirschsprung Disease , Child , Humans , Hirschsprung Disease/complications , Hirschsprung Disease/surgery , Quality of Life , Fecal Incontinence/diagnosis , Fecal Incontinence/etiology , Fecal Incontinence/therapy , Societies, Medical , North America
3.
J Pediatr Gastroenterol Nutr ; 74(5): 593-598, 2022 05 01.
Article in English | MEDLINE | ID: mdl-35192576

ABSTRACT

ABSTRACT: To characterize the current availability and scope of pediatric neurogastroenterology and motility (PNGM) services in North America (NA), the NASPGHAN-NGM committee distributed a self-reporting survey through the NASPGHAN bulletin board and mailing listserv, to compile a list of NA centers offering PNGM services, PNGM training, and the types of diagnostic and therapeutic PNGM procedures and services. We received responses that 54 centers in NA offer some form of PNGM services. Previously, the NASPGHAN website had last updated information from 2015 listing 36 centers in the USA and 2 in Canada. The American Neurogastroenterology and Motility Society (ANMS) website had 16 PNGM centers listed in NA in 2021. Neither of these resources capture additional information regarding training, research, advanced diagnostics, and therapeutics, and all available PNGM services. Our data highlights the growth in the field of PNGM services, and the variability of their distribution throughout the continent.


Subject(s)
Gastroenterology , Canada , Child , Gastroenterology/education , Humans , North America , Postal Service , Surveys and Questionnaires , United States
4.
Children (Basel) ; 8(12)2021 Dec 08.
Article in English | MEDLINE | ID: mdl-34943354

ABSTRACT

Preterm infants are known to have long-term healthcare needs. With advances in neonatal medical care, younger and more preterm infants are surviving, placing a subset of the general population at risk of long-term healthcare needs. Oral feeding problems in this population often play a substantial yet under-appreciated role. Oral feeding competency in preterm infants is deemed an essential requirement for hospital discharge. Despite achieving discharge readiness, feeding problems persist into childhood and can have a residual impact into adulthood. The early diagnosis and management of feeding problems are essential requisites to mitigate any potential long-term challenges in preterm-born adults. This review provides an overview of the physiology of swallowing and oral feeding skills, disruptions to oral feeding in preterm infants, the outcomes of preterm infants with feeding problems, and an algorithmic approach to the evaluation and management of neonatal feeding problems.

6.
Neurogastroenterol Motil ; 31(7): e13595, 2019 07.
Article in English | MEDLINE | ID: mdl-30957319

ABSTRACT

BACKGROUND: Nausea frequently co-exists with functional abdominal pain disorders (FAPDs) and may be linked to a higher disease burden. This study aimed to prospectively compare multisystem symptoms, quality of life, and functioning in FAPDs with and without nausea. METHODS: Adolescents ages 11-18 years fulfilling Rome III criteria for a FAPD were grouped by the presence or absence of chronic nausea. Subjects completed validated instruments assessing nausea (Nausea Profile Questionnaire = NPQ), quality of life (Patient-Reported Outcome Measurement Information System), functioning (Functional Disability Inventory), and anxiety (State-Trait Anxiety Inventory for Children). Group comparisons were performed for instruments, multisystem symptoms, school absences, and clinical diagnoses. KEY RESULTS: A total of 112 subjects were included; 71% reported chronic nausea. Patients with Nausea compared to No Nausea had higher NPQ scores (P ≤ 0.001), worse quality of life (P = 0.004), and greater disability (P = 0.02). State and trait anxiety scores were similar (P = 0.57, P = 0.25). A higher NPQ score correlated with poorer quality of life, more disability, and higher anxiety. Specific comorbidities were more common in Nausea vs No Nausea group: dizziness (81% vs 41%; P ≤ 0.001), concentrating difficulties (68% vs 27%; P ≤ 0.001), chronic fatigue (58% vs 20%; P = 0.01), and sleep disturbances (73% vs 48%; P = 0.02). The Nausea group reported more school absences (P = 0.001) and more commonly met criteria for functional dyspepsia (P = 0.034). CONCLUSION AND INFERENCES: Nausea co-existing with FAPDs is associated with a higher extra-intestinal symptom burden, worse quality of life, and impaired functioning in children. Assessing and targeting nausea therapeutically is essential to improve outcomes in FAPDs.


Subject(s)
Gastrointestinal Diseases/complications , Nausea/etiology , Nausea/psychology , Quality of Life , Abdominal Pain/complications , Abdominal Pain/psychology , Adolescent , Chronic Disease , Female , Humans , Male
8.
Trop Med Int Health ; 17(8): 962-71, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22686454

ABSTRACT

OBJECTIVE: To understand the health status of HIV orphans in a well-structured institutional facility in India. METHOD: Prospective longitudinal analysis of growth and anaemia prevalence among these children, between June 2008 and May 2011. RESULTS: A total of 85 HIV-infected orphan children residing at Sneha Care Home, Bangalore, for at least 1 year, were included in the analysis. Prevalence of anaemia at entry into the home was 40%, with the cumulative incidence of anaemia during the study period being 85%. At baseline, 79% were underweight and 72% were stunted. All children, irrespective of their antiretroviral therapy (ART) status, showed an improvement in nutritional status over time as demonstrated by a significant increase in weight (median weight-for-age Z-score: -2.75 to -1.74, P < 0.001) and height Z-scores (median height-for-age Z-score: -2.69 to -1.63, P < 0.001). CONCLUSION: These findings suggest that good nutrition even in the absence of ART can bring about improvement in growth. The Sneha Care Home model indicates that the holistic approach used in the Home may have been helpful in combating HIV and poor nutritional status in severely malnourished orphaned children.


Subject(s)
Anemia/epidemiology , Child Development , HIV Infections/blood , Nutritional Status , Orphanages/statistics & numerical data , Adolescent , Anti-Retroviral Agents/therapeutic use , Body Weights and Measures , CD4 Lymphocyte Count , Child , Child, Preschool , Female , HIV Infections/drug therapy , Humans , India/epidemiology , Longitudinal Studies , Male , Malnutrition/epidemiology
9.
Indian J Pediatr ; 79(12): 1666-8, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22294270

ABSTRACT

Hereditary Elliptocytosis is a heterogeneous group of disorder with regard to clinical presentation, protein defects and mode of inheritance. Parvoviral induced transient aplastic crisis in the form of sudden onset anemia is said to be a rare manifestation of this hereditary hemolytic anemia. The authors describe a case of parvoviral induced transient aplastic crisis in a patient with hereditary elliptocytosis and review the pathogenic mechanisms of parvoviral hemolytic disease.


Subject(s)
Anemia, Aplastic/diagnosis , Anemia, Aplastic/virology , Elliptocytosis, Hereditary/complications , Parvoviridae Infections/complications , Adolescent , Anemia, Aplastic/therapy , Diagnosis, Differential , Erythrocyte Transfusion , Humans , Male , Parvovirus B19, Human
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