Publications by authors named "Strong N"

Article Synopsis
  • * There has been a shift from infections primarily caused by drug-susceptible species to an increase in non-susceptible species, leading to greater treatment difficulties due to rising drug resistance.
  • * With more patients at risk due to advances in cancer treatment and the emergence of resistant strains of Candida, understanding these changes is crucial for developing effective management and prevention strategies.
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  • The study investigates the relationship between transvaginal cervical length (TVCL) measurements after cerclage placement and the risk of spontaneous preterm birth (sPTB).
  • It analyzes data from 210 patients with singleton pregnancies, focusing on the odds of sPTB in those with TVCL measurements less than 2.5 cm compared to those with measurements 2.5 cm or greater.
  • The results indicate that while a TVCL <2.5 cm does not significantly increase the odds of sPTB, a TVCL <2.0 cm is associated with significantly higher odds of sPTB.
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Study Objective: Evaluate the association between early naloxone use and outcomes after out-of-hospital cardiac arrest (OHCA) with initial non-shockable rhythms.

Methods: This study was a secondary analysis of data collected in the Portland Cardiac Arrest Epidemiologic Registry, a database containing details of emergency medical services (EMS)-treated OHCA cases in the Portland, Oregon metropolitan region. Eligible patients had non-traumatic OHCA with an initial non-shockable rhythm and received naloxone by EMS or law enforcement prior to IV/IO access (exposure group).

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Aim This study aims to assess the effect of implementing an enhanced prenatal genetic checklist to guide the provider's discussion on both screening and diagnostic options for fetal aneuploidy testing at the initial prenatal visit. Methods A retrospective quality improvement (QI) project was performed at a single, large, urban academic medical center. The implementation of this project was prospective; however, data was examined retrospectively after the QI initiative was implemented for three months.

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  • Fusarium species are becoming a significant cause of meningitis and invasive disease, particularly among immunocompromised and healthy individuals, as seen in recent outbreaks.
  • The frequency of these infections is rising, but advancements in molecular techniques are leading to faster diagnoses and promising new antifungal treatments.
  • Despite the increasing incidence of CNS fusariosis and its challenging prognosis, ongoing developments in diagnostics and treatment strategies may improve patient outcomes.
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Background: Accurate individualized assessment of preeclampsia risk enables the identification of patients most likely to benefit from initiation of low-dose aspirin at 12 to 16 weeks of gestation when there is evidence for its effectiveness, and enables the guidance of appropriate pregnancy care pathways and surveillance.

Objective: The primary objective of this study was to evaluate the performance of artificial neural network models for the prediction of preterm preeclampsia (<37 weeks' gestation) using patient characteristics available at the first antenatal visit and data from prenatal cell-free DNA screening. Secondary outcomes were prediction of early-onset preeclampsia (<34 weeks' gestation) and term preeclampsia (≥37 weeks' gestation).

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A multinational outbreak of nosocomial fusarium meningitis occurred among immunocompetent patients who had undergone surgery with epidural anesthesia in Mexico. The pathogen involved had a high predilection for the brain stem and vertebrobasilar arterial system and was associated with high mortality from vessel injury. Effective treatment options remain limited; in vitro susceptibility testing of the organism suggested that it is resistant to all currently approved antifungal medications in the United States.

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Objective: One goal of prenatal genetic screening is to optimize perinatal care and improve infant outcomes. We sought to determine whether high-risk cfDNA screening for 22q11.2 deletion syndrome (22q11.

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Background: Glanzmann thrombasthenia (GT) is a rare, autosomal recessive disorder of platelet glycoprotein IIb-IIIa receptors. Pregnant patients with GT are at increased risk of maternal and fetal bleeding. There is a paucity of literature on the peripartum management of patients.

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Objective: To investigate whether use of cognitive reappraisal and expressive suppression interact with childhood trauma burden to predict alcohol problems in a sample of American Indian adults.

Methods: Four hundred and twenty-nine American Indian adults (Mean age = 37.62, 59.

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  • Food allergies (FA) and atopic dermatitis (AD) often appear in infants, making it crucial to understand their causes for better prevention and treatment strategies.
  • The SunBEAm birth cohort, funded by NIAID, is a multi-center study in the US that follows pregnant couples and their newborns, aiming to enroll 2,500 infants to explore environmental and biological factors influencing FA and AD.
  • The cohort will collect a diverse range of samples and data, allowing researchers to examine the mechanisms behind early allergic reactions, focusing specifically on common allergens like egg, milk, and peanut.
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  • The American College of Obstetricians and Gynecologists recommends offering genetic screening and diagnostic testing to all pregnant individuals, yet there are gaps in understanding how demographics affect this process among prenatal care providers.
  • This study surveyed 635 outpatient prenatal care providers to explore their practices regarding offering diagnostic genetic testing and to analyze how patient and provider demographics influence these offerings.
  • Analyzing the responses, the study aimed to uncover disparities in genetic counseling practices during pregnancy, with a focus on associations related to provider training level, race, and insurance status.
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  • The study aimed to evaluate how effectively cell-free DNA (cfDNA) screening can detect sex chromosome aneuploidies (SCAs) in a diverse obstetrical population confirmed by genetics.
  • It analyzed data from the SMART study, focusing on cases involving monosomy X (MX) and sex chromosome trisomies (SCT), determining metrics like sensitivity and positive predictive value (PPV) for these conditions.
  • Results indicated high accuracy in fetal sex prediction (100%) and comparable screening performance for SCAs to existing literature, with notable differences in PPV between SCTs and MX, aiding in better interpretation of cfDNA results.
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Background: The clinical implications of nonreportable cell-free DNA screening results are uncertain, but such results may indicate poor placental implantation in some cases and be associated with adverse obstetrical and perinatal outcomes.

Objective: This study aimed to assess the outcomes of pregnancies with nonreportable cell-free DNA screening in a cohort of patients with complete genetic and obstetrical outcomes.

Study Design: This was a prespecified secondary analysis of a multicenter prospective observational study of prenatal cell-free DNA screening for fetal aneuploidy and 22q11.

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Gestational alloimmune liver disease is a rare complication associated with reactive maternal immunoglobulins resulting in neonatal liver pathology. The mainstay treatment for prevention in future pregnancies is intravenous immunoglobulins. Although relatively well tolerated, adverse reactions may occur.

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Background: Historically, prenatal screening has focused primarily on the detection of fetal aneuploidies. Cell-free DNA now enables noninvasive screening for subchromosomal copy number variants, including 22q11.2 deletion syndrome (or DiGeorge syndrome), which is the most common microdeletion and a leading cause of congenital heart defects and neurodevelopmental delay.

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Bastos ML, Perlman-Arrow S, Menzies D, Campbell JR. Ann Intern Med. 2021;174:501-10.

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Sporotrichosis is a mycotic infection caused by the Sporothrix schenckii species complex. It typically presents as a localized, mostly cutaneous or lymphocutaneous infection, but has been increasingly presenting as a disseminated infection in immunocompromised individuals, especially in HIV/AIDS patients. We also included a literature review of sporotrichosis in this patient population.

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The objectives were to determine whether cows previously classified during a postweaning test as either low or high residual feed intake (LRFI or HRFI) differed in BW, BCS, and winter grazing activity while consuming poor-quality forage. Thirty Hereford × Angus (LRFI = 16; HRFI = 14) 2-yr-old mid- to late-gestation cows (pregnant with second calf) grazed sagebrush steppe for 78 d beginning 29 September 2015. BW and BCS were collected before and after grazing.

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Desmogleins (Dsgs) are cadherin family adhesion molecules essential for epidermal integrity. Previous studies have shown that desmogleins associate with lipid rafts, but the significance of this association was not clear. Here, we report that the desmoglein transmembrane domain (TMD) is the primary determinant of raft association.

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Background: We investigated a novel surgical approach to decompressive craniectomy (DC), the bifrontal biparietal, or "cruciate," craniectomy, in severe pediatric traumatic brain injury (TBI). Cruciate DC was designed with a fundamentally different approach to intracranial pressure (ICP) control compared to traditional DC. Cruciate DC involves craniectomies in all 4 skull quadrants.

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Background Context: Stem cell-involved tissue engineering has gained dramatic attention as a therapeutic strategy for tissue regeneration including bone repair. However, the currently available possibilities to use embryonic stem cells and induced pluripotent stem cells (iPCs) face potential ethical issues, as well as risks of malignant transformation and immune rejection. Recently identified peripheral nerve-derived adult pluripotent stem cells (NEDAPS) that quickly proliferate after exposure to bone morphogenetic protein-2 (BMP-2) or nerve trauma and exhibit many embryonic stem cell characteristics may provide an attractive source cells for a variety of regenerative therapies.

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