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1.
Prehosp Disaster Med ; 32(4): 451-456, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28345508

ABSTRACT

Introduction A simple, portable capillary refill time (CRT) simulator is not commercially available. This device would be useful in mass-casualty simulations with multiple volunteers or mannequins depicting a variety of clinical findings and CRTs. The objective of this study was to develop and evaluate a prototype CRT simulator in a disaster simulation context. METHODS: A CRT prototype simulator was developed by embedding a pressure-sensitive piezo crystal, and a single red light-emitting diode (LED) light was embedded, within a flesh-toned resin. The LED light was programmed to turn white proportionate to the pressure applied, and gradually to return to red on release. The time to color return was adjustable with an external dial. The prototype was tested for feasibility among two cohorts: emergency medicine physicians in a tabletop exercise and second year medical students within an actual disaster triage drill. The realism of the simulator was compared to video-based CRT, and participants used a Visual Analog Scale (VAS) ranging from "completely artificial" to "as if on a real patient." The VAS evaluated both the visual realism and the functional (eg, tactile) realism. Accuracy of CRT was evaluated only by the physician cohort. Data were analyzed using parametric and non-parametric statistics, and mean Cohen's Kappas were used to describe inter-rater reliability. RESULTS: The CRT simulator was generally well received by the participants. The simulator was perceived to have slightly higher functional realism (P=.06, P=.01) but lower visual realism (P=.002, P=.11) than the video-based CRT. Emergency medicine physicians had higher accuracy on portrayed CRT on the simulator than the videos (92.6% versus 71.1%; P<.001). Inter-rater reliability was higher for the simulator (0.78 versus 0.27; P<.001). CONCLUSIONS: A simple, LED-based CRT simulator was well received in both settings. Prior to widespread use for disaster triage training, validation on participants' ability to accurately triage disaster victims using CRT simulators and video-based CRT simulations should be performed. Chang TP , Santillanes G , Claudius I , Pham PK , Koved J , Cheyne J , Gausche-Hill M , Kaji AH , Srinivasan S , Donofrio JJ , Bir C . Use of a novel, portable, LED-based capillary refill time simulator within a disaster triage context. Prehosp Disaster Med. 2017;32(4):451-456.


Subject(s)
Disasters , Mass Casualty Incidents , Oximetry/instrumentation , Triage , Equipment Design , Humans , Patient Simulation , Pilot Projects , Video Recording
2.
Pediatr Emerg Care ; 30(9): 613-6, 2014 Sep.
Article in English | MEDLINE | ID: mdl-25162691

ABSTRACT

OBJECTIVES: We compare the rate of return to the emergency department (ED) within 72 hours between families of children receiving a follow-up telephone call by a non-health care provider asking about the child's well-being 12 hours after their visit to the ED and families not receiving a follow-up call. METHODS: This was a prospective, randomized study in which we conducted a follow-up call starting at 12 hours after discharge from the ED versus no call for follow-up. At 96 hours after discharge, we contacted all recruited families. We recorded the rate of return to the ED within 72 hours of discharge. RESULTS: Of 371 families in the data analysis, 46% were in the study group, and 55.5% were male patients. Mean age was 5.7 years. The outcome measure was found to be in contrary to our hypothesis. We found return visits to the ED in 24 (14%) of the children in the study group compared with only 14 (7%) in the control group (P < 0.03). All other parameters were not statistically different between the groups. CONCLUSIONS: Emergency departments practicing follow-up calls by non-health care providers should consider a forecasted increase in return rates.


Subject(s)
Aftercare , Emergency Service, Hospital , Patient Readmission/statistics & numerical data , British Columbia , Child , Child, Preschool , Female , Follow-Up Studies , Humans , Male , Patient Discharge , Telephone
3.
Blood ; 113(25): 6342-50, 2009 Jun 18.
Article in English | MEDLINE | ID: mdl-19377048

ABSTRACT

Hematopoietic stem cells (HSCs) are generally defined by their dual properties of pluripotency and extensive self-renewal capacity. However, a lack of experimental clarity as to what constitutes extensive self-renewal capacity coupled with an absence of methods to prospectively isolate long-term repopulating cells with defined self-renewal activities has made it difficult to identify the essential components of the self-renewal machinery and investigate their regulation. We now show that cells capable of repopulating irradiated congenic hosts for 4 months and producing clones of cells that can be serially transplanted are selectively and highly enriched in the CD150(+) subset of the EPCR(+)CD48(-)CD45(+) fraction of mouse fetal liver and adult bone marrow cells. In contrast, cells that repopulate primary hosts for the same period but show more limited self-renewal activity are enriched in the CD150(-) subset. Comparative transcriptome analyses of these 2 subsets with each other and with HSCs whose self-renewal activity has been rapidly extinguished in vitro revealed 3 new genes (VWF, Rhob, Pld3) whose elevated expression is a consistent and selective feature of the long-term repopulating cells with durable self-renewal capacity. These findings establish the identity of a phenotypically and molecularly distinct class of pluripotent hematopoietic cells with lifelong self-renewal capacity.


Subject(s)
Cell Separation/methods , Flow Cytometry/methods , Hematopoietic Stem Cells/cytology , Animals , Animals, Congenic , Antigens, CD/analysis , Antigens, Differentiation/analysis , Bone Marrow Cells/cytology , Cell Division , Cells, Cultured/transplantation , Gene Expression Profiling , Hematopoietic Stem Cell Transplantation , Hematopoietic Stem Cells/metabolism , Immunophenotyping , Leukocyte Common Antigens/analysis , Liver/cytology , Liver/embryology , Mice , Mice, Inbred C57BL , Phospholipase D/analysis , Radiation Chimera , Receptors, Cell Surface/analysis , Signaling Lymphocytic Activation Molecule Family Member 1 , rhoB GTP-Binding Protein/analysis , rhoB GTP-Binding Protein/genetics , von Willebrand Factor/analysis , von Willebrand Factor/genetics
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