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1.
Clin Pract Cases Emerg Med ; 3(3): 312-313, 2019 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-31403106

RESUMO

Keratoconus is a progressive disorder affecting the cornea, which causes the cornea to become weakened and conical in appearance. The resultant decrease in structural integrity of the cornea predisposes affected individuals to acute corneal hydrops, a break in Descemet's membrane, the deepest layer of the cornea, resulting in pain and acute vision loss. We present here a case of this little-known cause of acute vision loss, and an example of Munson's sign, which is a v-shaped protrusion of the lower eyelid on downward gaze that is characteristic of advanced keratoconus. We hope to highlight Munson's sign as a simple identifier of keratoconus in an otherwise undiagnosed individual suspected of having acute corneal hydrops.

2.
West J Emerg Med ; 16(3): 372-80, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25987909

RESUMO

INTRODUCTION: The decision to treat pain in the emergency department (ED) is a complex, idiosyncratic process. Prior studies have shown that EDs undertreat pain. Several studies demonstrate an association between analgesia administration and race. This is the first Midwest single institution study to address the question of race and analgesia, in addition to examining the effects of both patient and physician characteristics on race-based disparities in analgesia administration. METHODS: This was a retrospective chart review of patients presenting to an urban academic ED with an isolated diagnosis of back pain, migraine, or long bone fracture (LBF) from January 1, 2007 to December 31, 2011. Demographic and medication administration information was collected from patient charts by trained data collectors blinded to the hypothesis of the study. The primary outcome was the proportion of African-Americans who received analgesia and opiates, as compared to Caucasians, using Pearson's chi-squared test. We developed a multiple logistic regression model to identify which physician and patient characteristics correlated with increased opiate administration. RESULTS: Of the 2,461 patients meeting inclusion criteria, 57% were African-American and 30% Caucasian (n=2136). There was no statistically significant racial difference in the administration of any analgesia (back pain: 86% vs. 86%, p=0.81; migraine: 83% vs. 73%, p=0.09; LBF: 94% vs. 90%, p=0.17), or in opiate administration for migraine or LBF. African-Americans who presented with back pain were less likely to receive an opiate than Caucasians (50% vs. 72%, p<0.001). Secondary outcomes showed that higher acuity, older age, physician training in emergency medicine, and male physicians were positively associated with opiate administration. Neither race nor gender patient-physician congruency correlated with opiate administration. CONCLUSION: No race-based disparity in overall analgesia administration was noted for all three conditions: LBF, migraine, and back pain at this institution. A race-based disparity in the likelihood of receiving opiate analgesia for back pain was observed in this ED. The etiology of this is likely multifactorial, but understanding physician and patient characteristics of institutions may help to decrease the disparity by raising awareness of practice patterns and can provide the basis for quality improvement projects.


Assuntos
Analgésicos Opioides/administração & dosagem , Negro ou Afro-Americano/estatística & dados numéricos , Disparidades em Assistência à Saúde , Hispânico ou Latino/estatística & dados numéricos , Dor/tratamento farmacológico , População Branca/estatística & dados numéricos , Dor nas Costas/tratamento farmacológico , Esquema de Medicação , Serviço Hospitalar de Emergência/estatística & dados numéricos , Fraturas Ósseas/complicações , Disparidades em Assistência à Saúde/estatística & dados numéricos , Humanos , Meio-Oeste dos Estados Unidos , Transtornos de Enxaqueca/tratamento farmacológico , Dor/etiologia , Medição da Dor , Relações Médico-Paciente , Padrões de Prática Médica , Estudos Retrospectivos
3.
Intern Emerg Med ; 10(2): 177-80, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25403843

RESUMO

[K+] < 3.5 mmol/L is reported to occur in approximately 4 % of patients with diabetic ketoacidosis (DKA.) Therefore, the American Diabetes Association (ADA) and Joint British Diabetes Societies (JBDS) recommend the assessment of [K+] before the initiation of insulin treatment to avoid the precipitation of morbid hypokalemia. The purpose of this study was to assess the incidence of hypokalemia in patients presenting to the emergency department (ED) with DKA. This was a multicenter retrospective, cross-sectional study at EDs with a combined annual adult census of 155,000. Adult patients diagnosed with DKA in the ED, or who were admitted from the ED and subsequently diagnosed with DKA as determined from the hospital electronic database between January 2008 and December 2008, were included for analysis if they had the following initial laboratory values: (1) serum glucose >13.9 mmol/L (250 mg/dL), (2) serum bicarbonate <18 mmol/L (18 mEq/L) or anion gap >15, and (3) evidence of ketonaemia or ketonuria. 537 patients were diagnosed with DKA in the ED at the participating institutions during the reference period. The median [K+] was 4.9 mmol/L (IQR 4.3, 5.5). There were a total of seven patients with an initial 3.3 < [K+] < 3.5 mmol/L, but none with a [K+] < 3.3 mmol/L. Thus, no patients in our study sample required potassium supplementation before the initiation of insulin treatment. The incidence of hypokalemia in our sample of patients with DKA was much less than previously reported, with no cases requiring potassium supplementation before insulin administration.


Assuntos
Cetoacidose Diabética/complicações , Hipopotassemia/diagnóstico , Estudos Transversais , Serviço Hospitalar de Emergência/estatística & dados numéricos , Hospitalização/estatística & dados numéricos , Humanos , Insulina/uso terapêutico , Potássio/uso terapêutico , Estudos Retrospectivos
4.
Am J Emerg Med ; 32(5): 457-60, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24529645

RESUMO

STUDY OBJECTIVE: The objective of this pilot study was to lay the groundwork for future studies assessing the impact of emergency physician-performed ultrasound (EPUS) on diagnostic testing and decision making in emergency department (ED) patients with nonspecific abdominal pain (NSAP). METHODS: This was a prospective, noninterventional study using a consecutive sample of patients presenting to the ED with NSAP as determined by nursing triage when a participating physician was available. Nonspecific abdominal pain was defined as abdominal pain for which the patient was seeking evaluation without a presumed diagnosis or referral for specific evaluation. Patients were evaluated by a physician who documented their differential diagnosis and planned diagnostic workup. Then, the physician performed EPUS, recorded their findings, and documented their post-EPUS differential diagnosis and planned diagnostic workup. This was compared with the patient's final diagnosis as determined by 2 emergency physicians blinded to the EPUS results. RESULTS: A total of 128 patients were enrolled. Fifty-eight (45%; 95% confidence interval [CI], 36%-54%) had an improvement in diagnostic accuracy and planned diagnostic workup using EPUS. Sixty-four (50%; 95% CI, 41%-59%) would have been treated without further radiographic imaging. Fifty (39%; 95% CI, 31%-48%) would have been treated without any further laboratory testing or imaging. DISCUSSION: Based on our findings, a future trial of 164 consecutive patients would have 90% power to confirm a 25% reduction in testing and a 25% improvement in decision making. CONCLUSION: Emergency physician-performed ultrasound appears to positively impact decision making and diagnostic workup for patients presenting to the ED with NSAP and should be studied further.


Assuntos
Dor Abdominal/diagnóstico por imagem , Serviço Hospitalar de Emergência , Adulto , Algoritmos , Tomada de Decisões , Diagnóstico Diferencial , Diagnóstico por Imagem/estatística & dados numéricos , Feminino , Humanos , Masculino , Projetos Piloto , Gravidez , Estudos Prospectivos , Triagem , Ultrassonografia
5.
J Emerg Med ; 41(6): 613-5, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-18547774

RESUMO

A 40-year-old woman presented via ambulance to our Emergency Department (ED) for decreased level of consciousness. The patient's husband reported declining cognitive ability over the prior 3 months, and a hospital visit for left leg weakness 5 months earlier. In the ED, the patient exhibited recurrent opisthotonus episodes. Old records obtained from another hospital were positive for reactive rapid plasma reagin test and florescent treponemal antibody absorption test (FTA-ABS). The patient's husband confirmed exposure to syphilis 15 years earlier. Subsequently, during hospitalization, the patient had a positive cerebrospinal fluid venereal disease research laboratory test and FTA-ABS, visible changes on a brain magnetic resonance imaging study, and was diagnosed with neurosyphilis.


Assuntos
Distúrbios Distônicos/etiologia , Neurossífilis/complicações , Adulto , Feminino , Humanos , Imageamento por Ressonância Magnética , Doenças Bacterianas Sexualmente Transmissíveis/líquido cefalorraquidiano
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