Publications by authors named "I Jordan"

Article Synopsis
  • - Cancer health disparities among different racial and ethnic groups burden health systems due to unequal access to early detection, treatment, and resources, resulting in worse outcomes and higher costs for advanced care.
  • - The study aims to evaluate the effectiveness of using genetic markers from the TruSight™ Hereditary Cancer Panel to assess global ancestry in 116 female cancer patients, comparing it with traditional genome-wide markers.
  • - Findings reveal a strong correlation in ancestry inference between the TruSight panel and whole genome sequencing, highlighting a mean genetic ancestry in the Colombian cohort of approximately 45.7% European, 46.2% Native American, and 8.11% African, indicating a promising method for exploring cancer disparities.
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Background: Despite growing evidence of reduced invasive and non-invasive pneumococcal disease attributed to public health measures against the COVID-19 pandemic, the effect of these measures on pneumococcal carriage remains unclear. This study aimed to assess pneumococcal nasopharyngeal carriage among children and adults self-confined at home during the COVID-19 national lockdown in Spain while identifying predictors of pneumococcal carriage in children.

Methods: Household study conducted across the metropolitan area of Barcelona (Spain) between April-June 2020.

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Infections caused by carbapenem-resistant Enterobacterales (CRE) are progressively increasing in Pediatric Intensive Care Units (PICUs). Its treatment is challenging due to the lack of pediatric trials. CRE infections are associated with significantly poor outcomes, but ceftazidime-avibactam (CAZ-AVI) has been reported to be successful in their treatment.

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Autosomal recessive conditions are often associated with homozygous mutations showing common ancestral origins and are frequently linked to consanguinity. However, an increasing number of compound heterozygotes are found in diverse, admixed populations. Oculocutaneous albinism (OCA) is a recessive condition caused mainly by mutations in the TYR and OCA2 genes involved in skin pigmentation.

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Background: Trust is a foundation of the therapeutic relationship and is associated with important patient outcomes. Building trust between parents of children with medical complexity (CMC) and physicians during inpatient care is complicated by lack of relational continuity, cumulative (sometimes negative) parent experiences and the need to adjust roles and expectations to accommodate parental expertise. This study's objective was to describe how parents of CMC conceptualize trust with physicians within the pediatric inpatient setting and to provide recommendations for building trust in these relationships.

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