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1.
Pediatr Rev ; 43(5): 285-287, 2022 05 01.
Article in English | MEDLINE | ID: mdl-35490201
3.
Front Pediatr ; 9: 679516, 2021.
Article in English | MEDLINE | ID: mdl-34336738

ABSTRACT

Introduction: Research capacity building is a critical component of professional development for pediatrician scientists, yet this process has been elusive in the literature. The ECHO IDeA States Pediatric Clinical Trials Network (ISPCTN) seeks to implement pediatric trials across medically underserved and rural populations. A key component of achieving this objective is building pediatric research capacity, including enhancement of infrastructure and faculty development. This article presents findings from a site assessment inventory completed during the initial year of the ISPCTN. Methods: An assessment inventory was developed for surveying ISPCTN sites. The inventory captured site-level activities designed to increase clinical trial research capacity for pediatrician scientists and team members. The inventory findings were utilized by the ISPCTN Data Coordinating and Operations Center to construct training modules covering 3 broad domains: Faculty/coordinator development; Infrastructure; Trials/Research concept development. Results: Key lessons learned reveal substantial participation in the training modules, the importance of an inventory to guide the development of trainings, and recognizing local barriers to clinical trials research. Conclusions: Research networks that seek to implement successfully completed trials need to build capacity across and within the sites engaged. Our findings indicate that building research capacity is a multi-faceted endeavor, but likely necessary for sustainability of a unique network addressing high impact pediatric health problems. The ISPCTN emphasis on building and enhancing site capacity, including pediatrician scientists and team members, is critical to successful trial implementation/completion and the production of findings that enhance the lives of children and families.

4.
Hawaii J Health Soc Welf ; 79(5 Suppl 1): 3-6, 2020 05 01.
Article in English | MEDLINE | ID: mdl-32490378

ABSTRACT

As one of 17 clinical sites of the Environmental influences on Child Health Outcomes (ECHO) IDeA States Pediatric Clinical Trials Network (ISPCTN), the Hawai'i IDeA Center for Pediatric and Adolescent Clinical Trials (HIPACT) was established in 2016 to participate in community-valued and scientifically-valid multi-center pediatric clinical trials to improve health and well-being of diverse multi-ethnic populations of Hawai'i. Hawai'i is home to large populations of diverse rural and underserved populations, including indigenous Hawaiian communities and immigrant populations of Pacific Islanders and Asians. Many of these communities experience significant health disparities, made worse by their geographic isolation and many socio-economic factors. In addition to providing opportunities for children and their families to participate in clinical trials, HIPACT's goal is to provide opportunities for junior faculty of the John A. Burns School of Medicine (JABSOM), University of Hawai'i at Manoa, to acquire knowledge about and to develop skills in clinical trials. HIPACT's partners include the Hawai'i Pacific Health with Kapi'olani Medical Center for Women and Children, and Waianae Coast Comprehensive Health Center. HIPACT builds on the experiences gained through partnerships with the Mountain West IDeA Clinical and Translational Research-Infrastructure Network, and Research Centers in Minority Institutions Translational Research Network. Apart from participating in ECHO ISPCTN-sponsored studies, HIPACT junior faculty serve as committee members, Working Group leaders, Protocol Study Principal Investigators (PI) and site study PIs with ECHO ISPCTN. Through participation in ECHO ISPCTN, HIPACT has successfully increased the number of pediatric and maternal-fetal medicine faculty involved in the conduct of clinical trials.


Subject(s)
Awards and Prizes , Clinical Trials as Topic/standards , Program Development/standards , Hawaii , Humans , Pediatrics/methods
5.
Hawaii J Health Soc Welf ; 79(5 Suppl 1): 64-70, 2020 05 01.
Article in English | MEDLINE | ID: mdl-32490388

ABSTRACT

Cat scratch disease is known to be a generally benign, self-resolving illness associated with non-specific symptoms, including lymphadenopathy, fever, fatigue, anorexia, and headaches. However, it can also cause disseminated disease with a wide range of manifestations, including liver and spleen microabscesses, osteomyelitis, encephalitis, and uveitis. Eighteen pediatric cases of disseminated cat scratch disease at a single center in Hawai'i are described. This case series emphasizes the importance of disease recognition and use of appropriate diagnostic tools and disease management. The disease burden of pediatric patients with disseminated cat scratch disease in the state of Hawai'i has a high incidence and should be considered in pediatric patients with prolonged febrile illnesses.


Subject(s)
Cat-Scratch Disease/complications , Pediatrics/statistics & numerical data , Adolescent , Cat-Scratch Disease/epidemiology , Cat-Scratch Disease/transmission , Child , Child, Preschool , Female , Hawaii/epidemiology , Humans , Infant , Liver/abnormalities , Liver/physiopathology , Male , Osteomyelitis/epidemiology , Osteomyelitis/etiology , Spleen/abnormalities , Spleen/physiopathology
7.
J Laparoendosc Adv Surg Tech A ; 23(4): 405-8, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23573888

ABSTRACT

Cases of rare-earth magnet ingestions have been increasingly reported in the literature. However, these descriptions have focused on the severity of the injuries, rather than the clinical presentation and/or therapeutic approach. We report a series of eight children, ranging in age from 2 to 10 years, who ingested powerful rare-earth magnets. The rare-earth magnets were marketed in 2009 under the trade name Buckyballs(®) (Maxfield & Oberton, New York, NY). They are about 5 mm in size, spherical, and brightly colored, making them appealing for young children to play with and place in their mouths. Three children presented within hours of ingestion, and the magnets were successfully removed via endoscopy in two, whereas the third child required laparoscopy. No fistulas were found in these children. A fourth child presented 2 days after ingestion with evidence of bowel wall erosion, but without fistula formation; the magnets were removed via laparoscopy. A fifth child ingested nine magnets in a ring formation, which were removed via colonoscopy without evidence of injury or fistula formation. The three remaining children presented late (5-8 days after ingestion) and were found to have associated fistulas. They were treated successfully with a combination of endoscopy and laparoscopy with fluoroscopy. None of the children in our series required an open surgical procedure. All children were discharged home without complications. This case series highlights the potential dangers of rare-earth magnet ingestion in children. Our experience suggests that prompt intervention using minimally invasive approaches can lead to successful outcomes.


Subject(s)
Endoscopy, Gastrointestinal , Foreign Bodies/surgery , Laparoscopy , Magnets , Metals, Rare Earth , Child , Child, Preschool , Eating , Humans , Remission Induction
8.
Pediatr Nephrol ; 22(8): 1225-7, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17377821

ABSTRACT

Schistosomiasis is a parasitic disease that can cause significant illness in humans. While schistosomiasis is not found in the United States and other developed countries, 200 million people are infected worldwide. It is estimated that 400,000 infected persons immigrate to the United States and present to emergency departments with either acute or chronic schistosomiasis. Schistosomiasis can be expected to be seen with increasing frequency in the United States and other developed countries with the continuing influx of immigrants, as well as the return of travelers and soldiers from endemic areas. Although there are several etiologies of gross hematuria in children, schistosomiasis is an uncommon cause of gross hematuria in the industrialized world. The purpose of this report is to bring awareness to health-care providers in the United States and other developed countries of this uncommon cause of gross hematuria, as prompt diagnosis and treatment can result in quick resolution of symptoms.


Subject(s)
Developed Countries , Hematuria/etiology , Schistosoma haematobium/parasitology , Schistosomiasis/diagnosis , Schistosomiasis/urine , Black or African American , Animals , Anthelmintics/therapeutic use , Black People , Child , Follow-Up Studies , Hematuria/parasitology , Humans , Male , Praziquantel/therapeutic use , Schistosomiasis/drug therapy , Siblings , Time Factors , Treatment Outcome , United States
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