Utilization of a pediatric emergency department by patients with sickle cell disease

1994 ◽  
Vol 10 (2) ◽  
pp. 79-82 ◽  
Author(s):  
NANETTE KUNKEL ◽  
WAYNE R. RACKOFF ◽  
LEONID KATOLIK ◽  
KWAKU OHENE-FREMPONG
Author(s):  
Wilson Andres Vasconez ◽  
Claudia Aguilar-Velez ◽  
Cristina Matheus ◽  
Hector Chavez ◽  
Roxana Middleton-Garcia ◽  
...  

2015 ◽  
Vol 22 (4) ◽  
pp. 423-430 ◽  
Author(s):  
Angela M. Ellison ◽  
Cary Thurm ◽  
Evaline Alessandrini ◽  
Shabnam Jain ◽  
John Cheng ◽  
...  

2017 ◽  
Vol 11 (08) ◽  
pp. 597-603
Author(s):  
Mariana Costa de Santana ◽  
Caroline Duarte Mello Amoedo ◽  
Cristiana Maria Nascimento-Carvalho

Introduction: Sepsis is a major cause of childhood death worldwide. In developing countries, epidemiological data about sepsis is scarce. This study describes and compares the frequency of etiological agents and initial sites of infection in children with or without sepsis, identifying risk factors and assessing outcomes. Methodology: Clinical and demographic data from patients < 13 years of age with reported fever in a pediatric emergency department were collected and registered in forms. Patients were classified as with or without sepsis according to Goldstein et al.’s criteria [6]. Results: Of 254 patients, 120 (47%) did and 134 (53%) did not meet the sepsis definition. Overall, the median age (IQR) was 1.7 (0.8–3.9) years, and 153 (60%) were boys. Patients with sepsis were older (2.8 [1.1–5.3] versus 1.3 [0.6–2.9] years; p < 0.001) and had sickle-cell disease more frequently (7.6% versus 0.8%; p = 0.007). By multiple logistic regression, age and sickle-cell disease were independently associated with sepsis. The most frequent initial infections were pneumonia (43.7%), diarrhea (17.3%) and cellulitis/adenitis (13.0%). The frequency of these did not differ when patients with or without sepsis were compared. Etiology was established in 57 (22.4%) patients, 32 (26.7%), and 25 (18.7%) with or without sepsis, respectively. Four (3.3%) patients died in the sepsis subgroup, whereas none died in the other subgroup. Conclusions: Children who met the 2005 international consensus definition of sepsis showed differences in age and comorbidities (sickle-cell disease) upon admission and were more likely to die.


2018 ◽  
Vol 48 (1) ◽  
pp. 59-74 ◽  
Author(s):  
Ashley Pantaleao ◽  
Joanne DiPlacido ◽  
Jessica W. Guite ◽  
William T. Zempsky

2018 ◽  
Vol 34 (8) ◽  
pp. 574-577 ◽  
Author(s):  
Katherine Eisenbrown ◽  
Angela M. Ellison ◽  
Mark Nimmer ◽  
Oluwakemi Badaki-Makun ◽  
David C. Brousseau

2020 ◽  
Vol 14 (1) ◽  
pp. 263-284
Author(s):  
Aindrea B. Maddray ◽  
Shannon M. Phillips

Background & Purpose: The purpose of this review is to examine instruments that measure providers' perceptions of adult patients with Sickle Cell Disease (SCD), examine instruments that measure adult patients with SCD perceptions of providers' behaviors, and determine optimal instruments to use in evaluating the perceptions of Emergency Department (ED) providers and adult patients with SCD of one another's behaviors after an interaction in the ED. Methods: An integrative review was conducted searching EBSCOhost and PubMed databases using the keywords: measure [OR] measure* [OR] assess* [OR] scale [OR] survey [OR] tool [AND] stigma* [OR] stereotype [OR] prejudice [OR] bias [OR] perception [OR] attitude [OR] discrimination [OR] racism [OR] behavior [AND] interaction [OR] relationship [OR] communication [AND] sickle cell. Initial search located 256 articles, but only 15 articles were included in the final review. Results: Fifteen articles reporting six instruments were reviewed. Four instruments evaluated a provider’s perceptions of patients with SCD behaviors, and two instruments evaluated how patients with SCD perceived provider behaviors. The two patient-focused instruments and three provider-focused instruments were found to be adequately reliable and valid according to the Psychometric Grading Framework (PGF). Conclusions: The findings suggest that the General Perceptions About Sickle Cell Disease Patients Scale would be an optimal instrument to evaluate ED providers' perceptions of adult patients with SCD behaviors. One patient-focused instrument, The Sickle Cell Health-Related Stigma Scale (SCD-HRSS), reported adequate reliability and validity but was not specific to measuring the patient's perceptions of ED providers' behaviors, nor was it administered in the ED environment. The SCD-HRSS Doctors subscale has potential adaptability for use in measuring patients with SCD perceptions of ED provider behaviors in the ED environment.


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