Objectives
In the Fluid and Catheter Treatment Trial (FACTT) of the National
Institutes of Health Acute Respiratory Distress Syndrome Network, a
conservative fluid protocol (FACTT Conservative) resulted in a lower
cumulative fluid balance and better outcomes than a liberal fluid protocol
(FACTT Liberal). Subsequent Acute Respiratory Distress Syndrome Network
studies used a simplified conservative fluid protocol (FACTT Lite). The
objective of this study was to compare the performance of FACTT Lite, FACTT
Conservative, and FACTT Liberal protocols.
Design
Retrospective comparison of FACTT Lite, FACTT Conservative, and FACTT
Liberal. Primary outcome was cumulative fluid balance over 7 days. Secondary
outcomes were 60-day adjusted mortality and ventilator-free days through day
28. Safety outcomes were prevalence of acute kidney injury and new
shock.
Setting
ICUs of Acute Respiratory Distress Syndrome Network participating
hospitals.
Patients
Five hundred three subjects managed with FACTT Conservative, 497
subjects managed with FACTT Liberal, and 1,124 subjects managed with FACTT
Lite.
Interventions
Fluid management by protocol.
Measurements and Main Results
Cumulative fluid balance was 1,918 ± 323 mL in FACTT Lite,
−136 ±491 mL in FACTT Conservative, and 6,992 ± 502
mL in FACTT Liberal (p < 0.001). Mortality was not
different between groups (24% in FACTT Lite, 25% in FACTT
Conservative and Liberal, p = 0.84).
Ventilator-free days in FACTT Lite (14.9 ±0.3) were equivalent to
FACTT Conservative (14.6±0.5) (p = 0.61)
and greater than in FACTT Liberal (12.1 ±0.5, p
< 0.001 vs Lite). Acute kidney injury prevalence was 58% in
FACTT Lite and 57% in FACTT Conservative (p
= 0.72). Prevalence of new shock in FACTT Lite (9%) was
lower than in FACTT Conservative (13%) (p =
0.007 vs Lite) and similar to FACTT Liberal (11%)
(p = 0.18 vs Lite).
Conclusions
FACTT Lite had a greater cumulative fluid balance than FACTT
Conservative but had equivalent clinical and safety outcomes. FACTT Lite is
an alternative to FACTT Conservative for fluid management in Acute
Respiratory Distress Syndrome.
Neutrophil recruitment to the alveolar space is associated with increased epithelial permeability. The present study investigated in mice whether neutrophil recruitment to the lung leads to accumulation of plasma-derived host defense proteins in the alveolar space and whether respiratory burst contributes to this increase in permeability. Albumin, complement C1q, and IgM were increased in bronchoalveolar lavage (BAL) fluid 6 h after intratracheal LPS challenge. Neutrophil depletion before LPS treatment completely prevented this increase in BAL fluid protein concentration. Respiratory burst was not detected in neutrophils isolated from BAL fluid, and BAL proteins were increased in mice deficient in a key subunit of the respiratory burst apparatus, gp91(phox), similar to wild-type mice. Neutrophil recruitment elicited by intratracheal instillation of the chemokines macrophage inflammatory protein-2 and keratinocyte-derived chemokine was also accompanied by accumulation of albumin, C1q, and IgM. During neutrophil recruitment to the alveolar space, epithelial permeability facilitates delivery of host defense proteins. The observed increase in epithelial permeability requires recruitment of neutrophils, but not activation of the respiratory burst, and occurs with chemokine-induced neutrophil migration independent of LPS exposure.
We describe the effect of simulation-based education on residents' adherence to protocols for and performance of central venous access.Methods: Internal medicine and emergency medicine residents underwent a central venous access course that included a lecture, video presentation, readings, and simulation demonstrations presented by faculty. Baseline data were collected before the course was initiated. After a skills session where they rehearsed their ultrasound-guided central venous access skills, residents were evaluated using a procedural checklist and written knowledge exam. Residents also completed questionnaires regarding confidence in performing ultrasound-guided central venous access and opinions about the training course.Results: Residents demonstrated significant improvement on the written knowledge exam (P < 0.0001) and Standard Protocol Checklist (P < 0.0001) after the training course. Training improved a number of patient safety elements, including adherence to sterile technique, transparent dressing, discarding sharps, and ordering postprocedure x-rays. However, a number of residents failed to wash their hands, prepare with chlorhexidine, drape the patient using a sterile technique, anesthetize the site, and perform a preprocedure time-out. Significant improvement in procedural skills was also noted for reduction in skin-to-vein time (P < 0.003) as well as a reduction in number of residents who punctured the carotid artery (P < 0.02).Conclusions: Simulation-based education significantly improved residents' knowledge and procedural skills along with their confidence. Adherence to the protocol also improved. This study illustrates that simulation-based education can improve patient safety through training and protocols.
Introduction. In December 2014, the Food and Drug Administration issued a recall of all Wallcur simulation products due to reports of their use in clinical practice. We present a case of septic shock and multiorgan failure after the accidental intravenous infusion of a nonsterile Wallcur simulation product. Case. The patient presented with symptoms of rigors and dyspnea occurring immediately after infusion of Wallcur Practi-0.9% saline. Initial laboratory evidence was consistent with severe septic shock and multiorgan dysfunction. His initial lactic acid level was 9 mmol/L (reference range = 0.5-2.2), and he had evidence of acute kidney injury and markers of disseminated intravascular coagulation. All 4 blood culture bottles isolated multidrug-resistant Empedobacter brevis. The patient recovered from his illness and was discharged with ciprofloxacin therapy per susceptibilities. Discussion. This patient represents the first described case of severe septic shock associated with the infusion of a Wallcur simulation product. Intravenous inoculation of a nonsterile fluid is rare and exposes the patient to unusual environmental organisms, toxins, or unsafe fluid characteristics such as tonicity. During course of treatment, we identified the possible culprit to be a multidrug-resistant isolate of Empedobacter brevis. We also discuss the systemic failures that led to this outbreak.
The majority of residents preferred the transverse approach to the longitudinal and oblique approaches. Although no significant differences among the 3 approaches were found in performance measures, more failures of technique occurred with the oblique approach. This study suggests that novices may require in-depth training and supervision to become proficient with the oblique approach.
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