Improving the Management of Vaso-Occlusive Episodes in the Pediatric Emergency Department.
نویسندگان
چکیده
OBJECTIVES Vaso-occlusive episodes (VOEs) account for the majority of emergency department (ED) visits for children with sickle cell disease (SCD). We hypothesized that addressing key barriers to VOE care would improve receipt of analgesics and outcomes. METHODS A quality improvement (QI) initiative was conducted from September 2010 to April 2014 to streamline VOE care in an urban pediatric ED. Four interventions were used: a standardized time-specific VOE protocol; intranasal fentanyl as the first parenteral pain medication; an SCD pain medication calculator; and provider and patient/family education. Data were collected for 3 outcome measures (mean time from triage to first parenteral opioid and admission/discharge decision, and proportion discharged from the ED); 1 process measure (mean time from triage to initiation of patient-controlled analgesia); and 4 balancing measures (mean time from triage to second intravenous opioid dose, 24-hour ED readmission, respiratory depression, and length of stay). RESULTS There were 289 ED visits in the study period. Improvements were seen in mean time to: first dose of parenteral opioid (56 to 23 minutes); second opiate intravenous dose (106 to 83 minutes); admission and discharge decisions (163 to 109 minutes and 271 to 178 minutes, respectively); and initiation of patient-controlled analgesia (216 to 141 minutes). The proportion discharged from the ED increased from 32% to 48% (χ(2) = 6.5402, P = .01). No increase in 24-hour readmission, respiratory depression, or inpatient length of stay was observed. CONCLUSIONS Using VOE-specific interventions, we significantly improved VOE care for children. Studies are needed to determine if these results can be replicated.
منابع مشابه
Sickle cell disease pain management in adolescents: a literature review.
Sickle cell disease (SCD) pain continues to emerge in adolescents. More than 98,000 individuals are believed to have SCD in the United States. In fact, 1 in 500 Black infants will be affected by SCD. Identifying standards of care for this unique population can improve pain management and treatment. A significant effect of vaso-occlusive crisis is a decrease in the quality of life in children. T...
متن کاملA randomized, placebo-controlled trial of arginine therapy for the treatment of children with sickle cell disease hospitalized with vaso-occlusive pain episodes.
Painful episodes of vaso-occlusion are the leading cause of hospitalizations and emergency department visits in sickle cell disease, and are associated with increased mortality. Low nitric oxide bioavailability contributes to vasculopathy in sickle cell disease. Since arginine is the obligate substrate for nitric oxide production, and an acute deficiency is associated with pain, we hypothesized...
متن کاملThe utility of routine reticulocyte count in uncomplicated vaso-occlusive events due to sickle cell disease
Labs are routinely ordered for patients admitted to the emergency room for uncomplicated vaso-occlusive events (VOE), however, there are no “standard” screening practices. Review articles and expert opinions regarding routine testing vary widely in their recommendations [1-3]. In addition, recent literature has called into question the need for routine screening laboratory analysis in clinicall...
متن کاملThe 844ins68 cystathionine beta-synthase and C677T MTHFR gene polymorphism and the vaso-occlusive event risk in sickle cell disease
INTRODUCTION Sickle cell disease (SCD) is an inflammatory condition with an increase in the adhesion of sickled erythrocytes, and it is a potential cause of vaso-occlusive episodes, an event related to clinical manifestations, morbidity and mortality. The cystathionine beta-synthase enzyme gene (CBS) and the methylenetetrahydrofolate reductase enzyme gene (MTHFR) are risk factors for thromboemb...
متن کاملRelationship between Depression, Anxiety, Quality of Life and Vaso-occlusive Crisis in Adolescents with Sickle Cell Disease
Aims: To explore the relationship between frequency of pain episodes and depression, anxiety, and health related quality of life (HRQOL) in adolescents with sickle cell disease (SCD). Materials and methods: Ten males and twelve females, between the ages of 12 and 19, selected during admittance to pediatric hematology outpatients of city hospital with a vaso-occlusive crisis in the period betwee...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Pediatrics
دوره 136 4 شماره
صفحات -
تاریخ انتشار 2015