Journal ArticleBiol Res Nurs · October 2024
Objective: Sickle cell disease (SCD), the most common inherited blood disorder in the United States, is associated with severe psychoneurological symptoms. While epigenetic age acceleration has been linked to psychoneurological symptom burden in other dise ...
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Journal ArticleThe journal of pain · August 2024
We aimed to determine the minimal clinically important difference (MCID) in pain severity and agreement between the visual analog scale (VAS) and the verbal numeric rating scale (NRS) in people with sickle cell disease (SCD) experiencing an acute vaso-occl ...
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Journal ArticlePediatr Blood Cancer · July 2024
BACKGROUND: National sickle cell disease (SCD) guidelines recommend oral hydroxyurea (HU) starting at 9 months of age, and annual transcranial Doppler (TCD) screenings to identify stroke risk in children aged 2-16 years. We examined prevalence and proporti ...
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Journal ArticleJ Pediatr Hematol Oncol · May 1, 2024
Adults and children with sickle cell disease (SCD) are predominantly African American, with pain-related health disparities. We examined opioid prescription fill patterns in adults and children with SCD and compared factors associated with fills in North C ...
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Journal ArticleJournal of the American Association of Nurse Practitioners · March 2024
BackgroundThe widespread use of telehealth and regulatory changes that enhanced nurse practitioner (NP) practice authority because of the SARS-CoV-2 pandemic offers an opportunity to assess postpandemic NP satisfaction with telehealth care deliver ...
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Journal ArticleJ Health Psychol · February 21, 2024
Diabetes distress (DD) is a negative psychosocial response to living with type 2 diabetes mellitus (T2DM). We sought insight into Veterans' experiences with DD in the context of T2DM self-management. The four domains in the Diabetes Distress Scale (i.e. re ...
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Journal ArticleBlood Adv · January 9, 2024
Sickle cell disease (SCD) affects ∼100 000 predominantly African American individuals in the United States, causing significant cellular damage, increased disease complications, and premature death. However, the contribution of epigenetic factors to SCD pa ...
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Journal ArticleJournal of Racial and Ethnic Health Disparities · January 1, 2024
Background/Objectives: This study is to (1) assess implicit racial bias among pediatric providers and (2) use virtual patient (VP) vignettes to determine the impact of implicit racial bias on clinical decision-making in pediatric sickle cell disease (SCD) ...
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Journal ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine · December 2023
BackgroundVaso-occlusive crises (VOCs) cause debilitating pain and are a common cause of emergency department (ED) visits, for people with sickle cell disease (SCD). Strategies for achieving optimal pain control vary widely despite evidence-based ...
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Journal ArticleBMC Health Services Research · December 1, 2023
Background: This study aimed to capture the implementation process of the ALIGN Study, (An individualized Pain Plan with Patient and Provider Access for Emergency Department care of Sickle Cell Disease). ALIGN aimed to embed Individualized Pain Plans in th ...
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Journal ArticlePediatr Blood Cancer · July 2023
OBJECTIVE: To describe the prevalence of infertility and infertility treatment seeking among people enrolled in the Sickle Cell Disease Implementation Consortium (SCDIC) registry and identify sociodemographic and clinical correlates of infertility. DESIGN: ...
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Journal ArticlePsychology, health & medicine · June 2023
Sickle cell disease (SCD) is the most common inherited blood disorder in both Jamaica and the United States and is characterized by poor quality of life and debilitating complications, with the hallmark symptom being pain caused by acute and chronic condit ...
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Journal ArticleEur J Haematol · May 2023
OBJECTIVE: Compare time to pain relief (minimum of a 13 mm and 30% reduction) during an Emergency Department (ED) visit among patients with sickle cell disease (SCD) experiencing severe pain associated with a vaso-occlusive episode who were randomized to r ...
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Journal ArticleBr J Haematol · March 2023
Individuals with sickle cell disease (SCD) have historically been considered underweight. Despite increasing body mass index (BMI) in the general population, the prevalence of overweight and obese status remains unclear in the adult SCD population. Our pri ...
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Journal ArticlePain Manag Nurs · February 2023
BACKGROUND: Pain is one of the most common and deleterious symptoms experienced by individuals with sickle cell disease (SCD). There is a paucity of studies identifying potential genetic mechanisms of pain in this population. AIM: Examine associations betw ...
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Journal ArticleBiol Res Nurs · January 2022
BACKGROUND: Severe pain is among the most common and deleterious symptoms experienced by individuals with sickle cell disease (SCD), of whom more than 50% report chronic pain. Despite this, the understanding of the biological contributors to persistent sev ...
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Journal ArticlePLoS One · 2022
INTRODUCTION: Sickle cell disease (SCD) is an inherited hemoglobinopathy that predominantly affects African Americans in the United States. The disease is associated with complications leading to high healthcare utilization rates, including emergency depar ...
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Journal ArticlePLoS One · 2022
Accruing evidence reveals best practices for how to help individuals living with Sickle Cell Disease (SCD); yet, the implementation of these evidence-based practices in healthcare settings is lacking. The Sickle Cell Disease Implementation Consortium (SCDI ...
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Journal ArticleBMJ open · November 2021
ObjectivesSickle cell disease (SCD) leads to chronic and acute complications that require specialised care to manage symptoms and optimise clinical results. The National Heart Lung and Blood Institute (NHLBI) evidence-based guidelines assist provi ...
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Journal ArticleBiol Res Nurs · October 2024
Objective: Sickle cell disease (SCD), the most common inherited blood disorder in the United States, is associated with severe psychoneurological symptoms. While epigenetic age acceleration has been linked to psychoneurological symptom burden in other dise ...
Full textLink to itemCite
Journal ArticleThe journal of pain · August 2024
We aimed to determine the minimal clinically important difference (MCID) in pain severity and agreement between the visual analog scale (VAS) and the verbal numeric rating scale (NRS) in people with sickle cell disease (SCD) experiencing an acute vaso-occl ...
Full textCite
Journal ArticlePediatr Blood Cancer · July 2024
BACKGROUND: National sickle cell disease (SCD) guidelines recommend oral hydroxyurea (HU) starting at 9 months of age, and annual transcranial Doppler (TCD) screenings to identify stroke risk in children aged 2-16 years. We examined prevalence and proporti ...
Full textLink to itemCite
Journal ArticleJ Pediatr Hematol Oncol · May 1, 2024
Adults and children with sickle cell disease (SCD) are predominantly African American, with pain-related health disparities. We examined opioid prescription fill patterns in adults and children with SCD and compared factors associated with fills in North C ...
Full textLink to itemCite
Journal ArticleJournal of the American Association of Nurse Practitioners · March 2024
BackgroundThe widespread use of telehealth and regulatory changes that enhanced nurse practitioner (NP) practice authority because of the SARS-CoV-2 pandemic offers an opportunity to assess postpandemic NP satisfaction with telehealth care deliver ...
Full textCite
Journal ArticleJ Health Psychol · February 21, 2024
Diabetes distress (DD) is a negative psychosocial response to living with type 2 diabetes mellitus (T2DM). We sought insight into Veterans' experiences with DD in the context of T2DM self-management. The four domains in the Diabetes Distress Scale (i.e. re ...
Full textOpen AccessLink to itemCite
Journal ArticleBlood Adv · January 9, 2024
Sickle cell disease (SCD) affects ∼100 000 predominantly African American individuals in the United States, causing significant cellular damage, increased disease complications, and premature death. However, the contribution of epigenetic factors to SCD pa ...
Full textOpen AccessLink to itemCite
Journal ArticleJournal of Racial and Ethnic Health Disparities · January 1, 2024
Background/Objectives: This study is to (1) assess implicit racial bias among pediatric providers and (2) use virtual patient (VP) vignettes to determine the impact of implicit racial bias on clinical decision-making in pediatric sickle cell disease (SCD) ...
Full textCite
Journal ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine · December 2023
BackgroundVaso-occlusive crises (VOCs) cause debilitating pain and are a common cause of emergency department (ED) visits, for people with sickle cell disease (SCD). Strategies for achieving optimal pain control vary widely despite evidence-based ...
Full textOpen AccessCite
Journal ArticleBMC Health Services Research · December 1, 2023
Background: This study aimed to capture the implementation process of the ALIGN Study, (An individualized Pain Plan with Patient and Provider Access for Emergency Department care of Sickle Cell Disease). ALIGN aimed to embed Individualized Pain Plans in th ...
Full textCite
Journal ArticlePediatr Blood Cancer · July 2023
OBJECTIVE: To describe the prevalence of infertility and infertility treatment seeking among people enrolled in the Sickle Cell Disease Implementation Consortium (SCDIC) registry and identify sociodemographic and clinical correlates of infertility. DESIGN: ...
Full textLink to itemCite
Journal ArticlePsychology, health & medicine · June 2023
Sickle cell disease (SCD) is the most common inherited blood disorder in both Jamaica and the United States and is characterized by poor quality of life and debilitating complications, with the hallmark symptom being pain caused by acute and chronic condit ...
Full textCite
Journal ArticleEur J Haematol · May 2023
OBJECTIVE: Compare time to pain relief (minimum of a 13 mm and 30% reduction) during an Emergency Department (ED) visit among patients with sickle cell disease (SCD) experiencing severe pain associated with a vaso-occlusive episode who were randomized to r ...
Full textOpen AccessLink to itemCite
Journal ArticleBr J Haematol · March 2023
Individuals with sickle cell disease (SCD) have historically been considered underweight. Despite increasing body mass index (BMI) in the general population, the prevalence of overweight and obese status remains unclear in the adult SCD population. Our pri ...
Full textLink to itemCite
Journal ArticlePain Manag Nurs · February 2023
BACKGROUND: Pain is one of the most common and deleterious symptoms experienced by individuals with sickle cell disease (SCD). There is a paucity of studies identifying potential genetic mechanisms of pain in this population. AIM: Examine associations betw ...
Full textLink to itemCite
Journal ArticleBiol Res Nurs · January 2022
BACKGROUND: Severe pain is among the most common and deleterious symptoms experienced by individuals with sickle cell disease (SCD), of whom more than 50% report chronic pain. Despite this, the understanding of the biological contributors to persistent sev ...
Full textLink to itemCite
Journal ArticlePLoS One · 2022
INTRODUCTION: Sickle cell disease (SCD) is an inherited hemoglobinopathy that predominantly affects African Americans in the United States. The disease is associated with complications leading to high healthcare utilization rates, including emergency depar ...
Full textLink to itemCite
Journal ArticlePLoS One · 2022
Accruing evidence reveals best practices for how to help individuals living with Sickle Cell Disease (SCD); yet, the implementation of these evidence-based practices in healthcare settings is lacking. The Sickle Cell Disease Implementation Consortium (SCDI ...
Full textOpen AccessLink to itemCite
Journal ArticleBMJ open · November 2021
ObjectivesSickle cell disease (SCD) leads to chronic and acute complications that require specialised care to manage symptoms and optimise clinical results. The National Heart Lung and Blood Institute (NHLBI) evidence-based guidelines assist provi ...
Full textCite
Journal ArticleSci Diabetes Self Manag Care · October 2021
PURPOSE: The purpose of this project was to identify additional facets of diabetes distress (DD) in veterans that may be present due to the veteran's military-related experience. METHODS: The study team completed cognitive interviews with veterans with typ ...
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Journal ArticleClin J Pain · September 1, 2021
OBJECTIVE: The aim of this study was to identify classes of individuals with sickle cell disease (SCD) who share distinct severe pain profiles and evaluate differences in demographic, clinical, and psychosocial characteristics between classes. METHODS: Thi ...
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Journal ArticleJ Immigr Minor Health · August 2021
Sickle cell disease (SCD) is a genetic disorder predominantly affecting people of African descent and is associated with significant morbidity and mortality. To improve SCD outcomes, the National Heart Lung and Blood Institute funded eight centers to parti ...
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Journal ArticleQualitative health research · July 2021
Sickle cell disease (SCD) is a chronic genetic disease that causes life-threatening complications and requires robust comprehensive management. Developing comprehensive SCD programs in sub-Saharan African countries requires knowledge of the cultural factor ...
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Journal ArticleJMIR Res Protoc · April 16, 2021
BACKGROUND: Individuals living with sickle cell disease often require aggressive treatment of pain associated with vaso-occlusive episodes in the emergency department. Frequently, pain relief is poor. The 2014 National Heart, Lung, and Blood Institute evid ...
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Journal ArticleCrit Care Nurs Q · April 2021
Sickle cell disease (SCD) is a common genetic blood disorder predominantly affecting African Americans in the United States. The objective of this study was to use a multimethods approach to describe how patients with SCD in North Carolina perceive the car ...
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Journal ArticleJournal of pediatric hematology/oncology · April 2021
IntroductionSickle cell disease (SCD) is the most common abnormal genetic blood disease that affects ∼100,000 Americans. Approximately 20% to 37% of children with sickle cell anemia have silent cerebral infarcts by the age of 14 years old. Neuroco ...
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Journal ArticleJ Health Econ Outcomes Res · April 1, 2021
Background: Sickle cell disease (SCD) is a genetic condition affecting primarily individuals of African descent, who happen to be disproportionately impacted by poverty and who lack access to health care. Individuals with SCD are at high likelihood of high ...
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Journal ArticleJ Pain Symptom Manage · March 2021
CONTEXT: Sickle cell disease (SCD), an autosomal recessive blood disorder, affects millions of people worldwide. Approximately 80% of all cases are located in Africa. OBJECTIVES: This cross-national, interdisciplinary, collaborative study investigated prov ...
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Journal ArticleContemporary clinical trials · February 2021
ObjectivesPainful vaso-occlusive episodes (VOE) are the most common reason for emergency department (ED) visits experienced by patients with sickle cell disease (SCD). The National Heart, Lung and Blood Institute (NHLBI) evidence-based recommendat ...
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Journal ArticleJ Emerg Nurs · January 2021
BACKGROUND: Sickle cell disease is associated with frequent vaso-occlusive episode and emergency department visits. Our group developed (1) a vaso-occlusive episode treatment algorithm based on the National Heart, Lung, and Blood Institute recommendations, ...
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Journal ArticleJournal of emergency nursing · January 2021
IntroductionIn 2016, the Ministry of Health in Jamaica selected the Emergency Severity Index as the triage tool to be used nationally. This study evaluated the effectiveness of this approach by assessing the interrater reliability among new users ...
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Journal ArticleN C Med J · 2021
BACKGROUND Sickle cell disease (SCD) is a complex disease associated with many complications and a shortened lifespan. In 2016, the National Heart, Lung and Blood Institute funded 8 centers in the United States to form the Sickle Cell Disease Implementatio ...
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Journal ArticleJ Prim Care Community Health · 2021
BACKGROUND: Sickle cell disease (SCD) is a complex chronic blood disorder characterized by severe disease complications ideally managed by both hematologists and primary care providers (PCP's). PCP's report knowledge gaps and discomfort with SCD management ...
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Journal ArticlePLoS One · 2021
INTRODUCTION: Sex-based clinical outcome differences in sickle cell disease (SCD) remain largely unknown despite evidence that female sex is associated with an increased lifespan. To better characterize sex-based differences in SCD, we assessed pain, treat ...
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Journal ArticleAnnals of emergency medicine · September 2020
Study objectiveGuided by an implementation science framework, this needs assessment identifies institutional-, provider-, and patient-level barriers to care of sickle cell disease (SCD) in the emergency department (ED) to inform future interventio ...
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Journal ArticleBlood advances · September 2020
Hydroxyurea is an efficacious treatment for sickle cell disease (SCD), but adoption is low among individuals with SCD. The objective of this study was to examine barriers to patients' adherence to hydroxyurea use regimens by using the intentional and unint ...
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Journal ArticlePediatric blood & cancer · May 2020
PurposeSickle cell disease (SCD) is associated with high acute healthcare utilization. The purpose of this study was to examine whether Medicaid expansion in California increased Medicaid enrollment, increased hydroxyurea prescriptions filled, and ...
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Journal ArticleJ Am Board Fam Med · 2020
BACKGROUND: Sickle-cell disease (SCD) causes significant morbidity, premature mortality, and high disease burden, resulting in frequent health care use. Comanagement may improve utilization and patient adherence with treatments such as Hydroxyurea. The pur ...
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Journal ArticleProfessional case management · September 2019
Purpose of studyThe purpose of the project was to describe the implementation and evaluation of a care management referral program from emergency departments (EDs) to care management services for patients with sickle cell disease (SCD).Primary ...
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Journal ArticleAdvanced emergency nursing journal · July 2019
Sickle cell disease (SCD) is a severe chronic disease that leads to premature mortality caused by serious complications of the disease such as acute chest syndrome, stroke, and sepsis. Patients presenting to the emergency department (ED) with pain due to v ...
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Journal ArticlePain Manag Nurs · June 2019
BACKGROUND: Few investigators have developed and tested nonpharmacological interventions for helping persons with sickle cell disease (SCD) manage persistent pain. AIMS: The purpose of this pilot study was to examine the feasibility and acceptability of a ...
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Journal ArticleThe American journal of nursing · June 2019
: Sickle cell disease (SCD) is an autosomal recessive genetic condition that alters the shape and function of the hemoglobin molecule in red blood cells. While the overall survival rate among children with SCD has improved in recent years, pediatric rates ...
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Journal ArticleMedical teacher · March 2019
A disease-focused course entitled "Understanding Sickle Cell Disease: A Biopsychosocial Approach" addressed the complex nature of SCD using patient-centered, global and interdisciplinary approaches. Sickle cell disease (SCD) is a rare inherited blood disor ...
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Journal ArticlePediatr Blood Cancer · January 2019
BACKGROUND: Sickle cell disease (SCD) is a chronic blood disorder in which mortality has increased for adolescents and young adults (AYA). PROCEDURE: A longitudinal analysis of medical records was conducted to describe the clinical course among AYAs (ages ...
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Journal ArticleAdv Emerg Nurs J · 2019
Treatment of vaso-occlusive episodes (VOEs) is the most common reason for emergency department (ED) treatment of sickle cell disease (SCD). We (1) compared perceptions of the usability and ability to manage VOE pain between ED nurses and other ED provider ...
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Journal ArticlePLoS One · 2019
BACKGROUND: Sickle cell disease (SCD) is an inherited blood disorder associated with acute pain crisis and other complications that lead to frequent emergency department (ED) visits. To improve outcomes, the National Heart, Lung and Blood Institute (NHLBI) ...
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Journal ArticlePilot and feasibility studies · January 2019
BackgroundThe purpose of this study was to pilot test two sickle cell-specific instruments, the Adult Sickle Cell Quality of Life Measurement Information System (ASCQ-Me) and Jenerette Self-Care Assessment Tool (J-SAT), to determine recruitment ra ...
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Journal ArticleIssues in mental health nursing · August 2018
The aim of this systematic review was to synthesize the literature regarding health-related stigma in adolescents and adults living with sickle cell disease (SCD). Four domains were identified from 27 studies: (1) social consequences of stigma; (2) the eff ...
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Journal ArticleProfessional case management · July 2018
Purpose and objectivesThe purpose of this discussion is to review the barriers to care for patients with sickle cell disease (SCD). Chronic pain and the perception of addiction, implicit bias, frequent hospitalizations and emergency department vis ...
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Journal ArticleThe American journal of hospice & palliative care · June 2018
PurposeTo examine bereaved parents' physical, mental, and social health during the first 6 months after their child's (<12 years) death from a life-threatening illness.Background and significanceBereaved parents have higher mortality and ...
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Journal ArticleThe western journal of emergency medicine · March 2018
IntroductionUse of alternative venues to manage uncomplicated vaso-occlusive crisis (VOC), such as a day hospital (DH) or ED observation unit, for patients with sickle cell anemia, may significantly reduce admission rates, which may subsequently r ...
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Journal ArticleAm J Hematol · February 2018
Limited evidence guides opioid dosing strategies for acute Sickle Cell (SCD) pain. We compared two National Heart, Lung and Blood (NHBLI) recommended opioid dosing strategies (weight-based vs. patient-specific) for ED treatment of acute vaso-occlusive epis ...
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Journal ArticleJournal of health care for the poor and underserved · January 2018
The purposeto determine frequency of health care encounters among people with sickle cell disease (SCD) seeking treatment for a vaso-occlusive crisis (VOC). Health care encounters are categorized by visit type (day hospital, ED visit, hospitalizat ...
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Journal ArticleJournal of emergency nursing · September 2017
IntroductionSickle cell disease (SCD) is a complex illness with many social-behavioral co-morbidities. The aim of this project was to describe unmet social-behavioral health needs for adults with SCD who presented to the emergency department for t ...
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Journal ArticleTrials · May 2017
BackgroundOne of the most difficult symptoms for persons with sickle cell disease (SCD) to manage is chronic pain. Chronic pain impacts approximately one-third of persons with SCD and is associated with increased pain intensity, pain behavior, and ...
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Journal ArticleJoint Commission journal on quality and patient safety · March 2017
BackgroundGuidelines recommend rapid, aggressive management of vaso-occlusive crisis (VOC) for patients with sickle cell disease (SCD). A large prospective research and quality improvement (QI) project was conducted to measure changes in clinical ...
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ConferenceBlood · December 2, 2016
AbstractIntroduction: Vaso-occlusive episodes are the most common complication experienced by individuals with sickle cell disease (SCD). Treatment in an emergency department (ED) i ...
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Journal ArticleAdvanced emergency nursing journal · October 2016
The purpose of this study is to identify the unique educational needs of emergency nurse practitioners (ENPs). A survey from 167 nurse practitioners (NPs) practicing in the emergency department (ED) settings was analyzed. A variety of certified NPs practic ...
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Journal ArticleJournal of emergency nursing · September 2016
ProblemVeterans eligible for health care in the Veterans Administration (VA) health system often receive care in community emergency Departments. In line with initiatives from Joining Forces and the American Academy of Nursing, emergency departmen ...
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Journal ArticleAdvanced emergency nursing journal · July 2016
Patients with sickle cell disease frequently seek care in the emergency department. They have reported experiencing negative attitudes from emergency providers. This study was undertaken to evaluate change in emergency provider attitudes toward patients wi ...
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Journal ArticlePain management nursing : official journal of the American Society of Pain Management Nurses · June 2016
Sickle cell disease (SCD) is a genetic disease associated with both chronic pain and acute painful events referred to as vaso-occlusive crises. Individuals with SCD suffer from a multitude of medical complications in addition to pain. Patients often are st ...
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Journal ArticleAdvanced emergency nursing journal · April 2016
Sickle cell disease (SCD) is a complex multisystem debilitating disease. Despite its complexity, health care providers who are not SCD experts receive little formal education on SCD. An open-access, educational website, "Emergency Department Sickle Cell Di ...
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Journal ArticleJournal of pain and symptom management · February 2016
ContextSickle cell disease (SCD) is a life-threatening condition that affects more than seven million people worldwide. The most common complication experienced by persons living with SCD is pain. Evidence supports the use of nonpharmacologic ther ...
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Journal ArticleJ Pediatr Nurs · 2016
UNLABELLED: This study explored the challenges faced by adolescents with sickle cell disease (SCD) and their parents and the work they engage in to progressively shift from parent management to independent adolescent self-management. DESIGN AND METHODS: A ...
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Journal ArticleJournal of holistic nursing : official journal of the American Holistic Nurses' Association · September 2015
The aim of this article is to discuss how advanced practice nurses (APNs) can incorporate mindfulness-based stress reduction (MBSR) as a nonpharmacologic clinical tool in their practice. Over the last 30 years, patients and providers have increasingly used ...
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Journal ArticleJournal of emergency nursing · May 2015
IntroductionA nurse-initiated high dose, opioid protocol for vaso-occlusive crisis (VOC) was implemented. Total intravenous morphine sulfate equivalents (IVMSE) in mgs] and safety was evaluated.MethodsA medical record review was conducted ...
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Journal ArticleAdvanced emergency nursing journal · October 2014
Patients with sickle cell disease (SCD) often seek care in the emergency department (ED) for pain associated with vaso-occlusive crises. Research has shown that negative provider attitudes serve as a barrier to care in this patient population. Our aim was ...
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Journal ArticleJAMA · September 10, 2014
IMPORTANCE: Sickle cell disease (SCD) is a life-threatening genetic disorder affecting nearly 100,000 individuals in the United States and is associated with many acute and chronic complications requiring immediate medical attention. Two disease-modifying ...
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Journal ArticleThe western journal of emergency medicine · July 2014
IntroductionPatients with sickle cell disease (SCD) often seek care in emergency departments (EDs) for severe pain. However, there is evidence that they experience inaccurate assessment, suboptimal care, and inadequate follow-up referrals. The aim ...
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Journal ArticleThe Nurse practitioner · April 2014
A clinical practice guideline for uncomplicated urinary tract infections in an ambulatory urgent care practice was implemented. Aims were to increase the number of first-line antibiotics prescribed to treat uncomplicated urinary tract infections, increase ...
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Journal ArticleJournal of emergency nursing · January 2014
IntroductionProviding a screening, brief intervention, and referral for treatment (SBIRT) may encourage patients to obtain provider follow-up for definitive evaluation and treatment of undiagnosed hypertension (HTN). The aims of this study were to ...
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Journal ArticleJ Emerg Nurs · November 2013
OBJECTIVE: (1) Determine the difference in pre-test and post-test knowledge scores for attendees of a train-the-trainer workshop and (2) determine the number of attendees who disseminated the content within 6 months of attending the workshop. METHODS: A 1- ...
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Journal ArticleJournal of emergency nursing · November 2013
ObjectivesPrevious research indicates that patients have difficulty understanding ED discharge instructions; these findings have important implications for adherence and outcomes. The objective of this study was to obtain direct patient input to i ...
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Journal ArticleAnnals of emergency medicine · October 2013
Study objectiveWe determine whether emergency provider attitudes and demographics are associated with adherence to national guidelines for the management of acute sickle cell disease pain.MethodsWe conducted a cross-sectional survey of em ...
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Journal ArticleJournal of pediatric oncology nursing : official journal of the Association of Pediatric Oncology Nurses · July 2013
Children with sickle cell disease (SCD) present to the emergency department (ED) with complex medical and behavioral health needs. Little research has been conducted to understand elements necessary to provide a comprehensive approach. We conducted 9 focus ...
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Journal ArticleThe American journal of emergency medicine · April 2013
Study objectiveTo determine whether patients with sickle cell disease (SCD) experience longer wait times to see a physician after arrival to an emergency department (ED) compared to patients with long bone fracture and patients presenting with all ...
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Journal ArticleAdvanced emergency nursing journal · April 2013
Emergency department (ED) management of adults with sickle cell disease (SCD) is complex and frustrating. The Emergency Department Sickle Cell Assessment of Needs and Strengths (ED-SCANS) is a research-based decision support and quality improvement (QI) to ...
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Journal ArticleJournal of the National Medical Association · September 2012
Patients with sickle cell disease (SCD) experience painful crises that often require admission to the emergency department (ED) for pain management. Factors such as ED overcrowding and negative perception and stigmatization of SCD may impact patients' perc ...
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Journal ArticleJournal of emergency nursing · May 2012
IntroductionOpioid abuse and overdose have increased drastically in recent years. Diversion of opioids used to treat pain, either through theft or sharing, is increasing and may contribute to this misuse. Based on these trends, we designed a study ...
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Journal ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine · April 2012
ObjectivesThe aims of this study were to 1) estimate differences in pain management process and patient-reported outcomes, pre- and postimplementation of analgesic protocols for adults with sickle cell disease (SCD), and 2) examine the effects of ...
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Journal ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine · January 2012
ObjectivesPatient acuity triage systems can play an important role in supporting patient safety and emergency department (ED) operations. In 2003, the boards of the American College of Emergency Physicians (ACEP) and the Emergency Nurses Associati ...
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Journal ArticleJournal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing · June 2011
PurposeNurse Practitioners (NPs) are certified within a population-focused specialty area, practice in a variety of settings, and treat a wide range of patients. Little is known about what agreement exists between certification obtained and actual ...
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Journal ArticleJournal of Nursing Regulation · January 1, 2011
An important advantage of survey research is its flexibility. Surveys can be used to conduct large national studies or to query small groups. Surveys can be made up of a few unstructured questions or can involve a large-scale, multisite longitudinal study ...
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Journal ArticleJournal of emergency nursing · January 2011
ObjectivesWe describe clinician-reported knowledge of the Joint National Committee (JNC7) on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure definitions of Stage I hypertension; perceived causes of elevated blood pressure; ...
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Journal ArticleAnnals of emergency medicine · December 2010
Study objectiveWe test an initiative with the staff-based participatory research (SBPR) method to elicit communication barriers and engage staff in identifying strategies to improve communication within our emergency department (ED).Methods
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Journal ArticleJournal of the National Medical Association · November 2010
BackgroundSickle cell disease (SCD) is associated with serious comorbidities resulting in a shortened lifespan, and many clients suffer from frequent pain episodes. However, others successfully manage their disease in the outpatient setting withou ...
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Journal ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine · August 2010
ObjectivesA decision support tool may guide emergency clinicians in recognizing assessment, analgesic and overall management, and health service delivery needs for patients with sickle cell disease (SCD) in the emergency department (ED). We aimed ...
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Journal ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine · April 2010
ObjectivesThe objectives were to report the baseline (prior to quality improvement interventions) patient and visit characteristics and analgesic management practices for each site participating in an emergency department (ED) sickle cell learning ...
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Journal ArticleThe Clinical journal of pain · March 2010
ObjectivesTo determine whether there is a difference in time to initial analgesic for patients with acute pain from sickle cell disease (SCD) versus renal colic (RC) and to identify factors contributing to variance in time to analgesic.Methods ...
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Journal ArticleBlood pressure monitoring · December 2009
ObjectivesTo determine blood pressure (BP) reassessment rates and to describe the evaluation and outpatient referral rates of elderly emergency department (ED) patients with elevated BP.MethodsThis was a retrospective cohort of patients w ...
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Journal ArticleJournal of emergency nursing · July 2009
IntroductionIntravenous (IV) catheter placement is an extremely common painful procedure performed in all ages and healthcare settings, more often than not without anesthetics, despite clear research and guidelines demonstrating their effectivenes ...
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Journal ArticleJournal of emergency nursing · July 2009
IntroductionIn our facility an operational process intervention was implemented to decrease overcrowding. The intervention consisted of implementing criteria (developed from a series of 8 interactive workshops led by the investigators with all cha ...
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Journal ArticleAmerican journal of hypertension · June 2009
BackgroundWe attempted to identify patient factors associated with blood pressure (BP) reassessment and to compare health-care provider self-reported reassessment and referral to actual practice in an emergency department (ED) setting.Methods< ...
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Journal ArticlePain medicine (Malden, Mass.) · March 2009
ObjectivePain is a complex experience influenced by factors such as age, race, and ethnicity. We conducted a multicenter study to better understand emergency department (ED) pain management practices and examined the influence of patient and provi ...
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Journal ArticlePatient education and counseling · November 2008
ObjectiveEffective communication is an essential aspect of high-quality patient care and a core competency for physicians. To date, assessment of communication skills in team-based settings has not been well established. We sought to tailor a psyc ...
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Journal ArticleThe American journal of emergency medicine · October 2008
ObjectivesThe aim of the study was to examine the association between triage scoring systems and triage priority scores on time to initial emergency department (ED) analgesic administration.MethodsAn observational, multicenter, prospectiv ...
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Journal ArticleJournal of emergency nursing · October 2008
IntroductionOur objective was to examine gender, racial, and age differences in door-to-EKG time in patients diagnosed with non-cardiac chest pain.MethodsThis was a prospective cohort study of adult patients with an explicitly stated chie ...
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Journal ArticleJournal of emergency nursing · August 2008
IntroductionThe purpose of this project was to develop operational criteria to "close the ED waiting room".MethodsA prospective, staff-based participatory research model was used. Nurses at an urban ED with 70,000 visits attended a four-h ...
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Journal ArticleAdvanced Emergency Nursing Journal · April 1, 2008
The Research to Practice column attempts to serve 2 purposes: (1) fine-tune the research critique skills of advanced practice nurses and (2) suggest strategies to translate findings from a research study into bedside practice. For each column, a topic and ...
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Journal ArticleAnnals of emergency medicine · March 2008
Study objectiveWe determine the proportion of patients with increased emergency department (ED) blood pressure and no history of hypertension who have persistently increased blood pressure at home, describe characteristics associated with sustaine ...
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Journal Article · January 1, 2008
SCOPE OF THE PROBLEM Emergency departments (EDs) face many challenges. Recent data suggest that patient visits in United States EDs have increased 18% over the past 10 years and are now estimated to approximate 110 million visits annually. Pain is the most ...
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Journal ArticleAdvanced Emergency Nursing Journal · January 1, 2008
The Research to Practice column selects a research article with important meaning for the advanced practice nurse. The column first discusses why the topic is important, and then provides a summary and critique of the research methods. Finally, the finding ...
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Journal ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine · November 2007
ObjectivesTo determine if dissemination of the American College of Emergency Physicians clinical policy on hypertension to emergency physicians would lead to improvements in blood pressure reassessment and referral of emergency department (ED) pat ...
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Journal ArticleED Nursing · July 1, 2007
Patients with sickle cell disease coming to EDs with an acute pain episode waited an average of 90 minutes for the first analgesic to be given, says a new study. • Patients may not appear to be in severe pain because they have chronic pain. • High triage s ...
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Journal ArticleThe journal of pain · June 2007
UnlabelledPain is the most common reason for emergency department (ED) use, and oligoanalgesia in this setting is known to be common. The Joint Commission on Accreditation of Healthcare Organizations has revised standards for pain management; howe ...
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Journal ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine · May 2007
ObjectivesTo characterize the initial management of patients with sickle cell disease and an acute pain episode, to compare these practices with the American Pain Society Guideline for the Management of Acute and Chronic Pain in Sickle-Cell Diseas ...
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Journal ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine · June 2005
ObjectivesThe Emergency Severity Index (ESI) version 3 is a five-level triage acuity scale with demonstrated reliability and validity. Patients are rated from ESI level 1 (highest acuity) to ESI level 5 (lowest acuity). Clinical experience has dem ...
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Journal ArticleJournal of emergency nursing · June 2004
IntroductionHypertension is often undiagnosed, untreated, undertreated, and poorly controlled. Many patients use the emergency department as their primary source of health care, and the emergency department represents an opportunity to identify un ...
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Journal ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine · June 2004
ObjectivesTo compare pain and discomfort ratings of female patients undergoing urethral catheterization randomized to topical application of plain lubricant versus lidocaine gel prior to the procedure.MethodsThis was a prospective, random ...
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Journal ArticleJournal of emergency nursing · February 2004
ObjectivesThe Emergency Severity Index (ESI) version 3 is a valid and reliable 5-level triage instrument that is gaining in popularity. A unique component of the ESI algorithm is prediction of resource consumption. Our objective was to validate th ...
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Journal ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine · January 2004
ObjectivesNo widely used triage instrument accurately assesses patient acuity. The Emergency Severity Index (ESI) promises to facilitate reliable acuity assessment and possibly predict patient disposition. However, reliability and validity of ESI ...
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Journal ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine · August 2003
ObjectivesTo evaluate simultaneously several possible risk factors for blood bank specimen hemolysis.MethodsThis was a prospective cohort study of emergency department and labor and delivery patients to estimate the effect of various fact ...
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Journal ArticleJournal of emergency nursing · April 2001
ObjectiveThe purposes of this study were to determine the most effective nursing intervention to decrease pain for patients with minor musculoskeletal trauma and moderate pain at triage and to examine patient satisfaction.MethodsPatients ...
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Journal ArticleJournal of emergency nursing · August 2000
IntroductionThe purpose of this study was to determine areas of emergency nurses' knowledge deficit regarding pain management, and to identify barriers to pain management as perceived by emergency nurses.MethodsData were collected anonymo ...
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Journal ArticleJournal of emergency nursing · June 1999
ObjectiveThis study was conducted to describe the prevalence of pain in the emergency department and to identify factors that may contribute to its treatment.MethodsInterviews were conducted with 203 patients who entered the emergency dep ...
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