β-lactams (e.g., #meropenem), are typically given intermittently, but continuous administration can provide constant serum levels and may improve outcomes.
In fact, several meta-analyses reported reduced mortality when administered continuously.
3/
Therefore, we conducted a multinational, double-blind, randomized controlled trial to test the hypothesis that continuous administration of #meropenem, compared with intermittent administration, would improve clinically relevant outcomes in critically ill pts with #sepsis
4/
P: ICU patients with sepsis or septic shock who needed new meropenem treatment
I: continuous infusion (3g/day)
C: intermittent administration (1g q8h)
O: composite of mortality and/or the emergence of pandrug-resistant or extensively drug-resistant bacteria at day 28
5/
A total of 607 patients were randomized, 303 in the continuous and 304 in the intermittent arm.
The two arms are well-balanced
64 years old
61% with septic shock
Time from hospital admission to randomization = 9 days
6/
The daily dose of meropenem was 3 g in both groups.
At randomization, 74% received concurrent antibiotic therapy, with glycopeptide being the most common.
Among patients with identified bacteria (71%), Klebsiella and Pseudomonas are the common gram-negative species.
7/
The primary outcome (mortality and/or emergence of PDR/XDR bacteria) was not significantly different between the two arms (47% vs 49%; RR 0.96 [95% CI 0.81–1.13]).
No interaction was found in any subgroup analysis.
In critically ill patients with sepsis, compared with intermittent administration, the continuous administration of meropenem did not improve the composite outcome of mortality and pan or extensively drug-resistance emergence.
10/
It's our honor to publish the results of #MERCYtrial in JAMA @JAMA_current: Continuous vs Intermittent Meropenem Administration in Critically Ill Patients with Sepsis
We thank all the patients, families, funder, investigators, and clinicians.
We also appreciate the editors/reviewers of @JAMA_current and @CritCareReviews for giving us the opportunity for the simultaneous publication/presentation.
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P: Critically ill patients
I: #Etomidate as an induction agent for intubation
C: Any comparator
O: Mortality at the main timepoint defined by authors
S: Randomized controlled trials
P: adults with #COVID19 not receiving oxygen
I: intravenous or oral #glucocorticoids
C: any
O: all-cause mortality at the longest follow-up available
S: RCTs, matched studies
➡️ 5 RCTs and 1 propensity-matched study (total 6634 pts) were included
Here we report the 1st case of intraoperative use of VA-#ECMO in a patient with resectable lung cancer and bivasal critical coronary artery disease with prohibitive low EF (23%), and describe the benefits of this new indication.
Cardiovascular comorbidities often prevent patients with otherwise resectable early-stage lung cancer from undergoing surgery due to prohibitive peri-operative risk.
In non-COVID-19 pneumonia/ARDS filling defects are found in pulmonary arteries branches vascularizing healthy lung segments. Instead, in #COVID19 there is an almost perfect topographical overlap of filling defects distribution & pneumonia extent.
We demonstrated that pulmonary vascular thrombosis in #COVID19 is due to local inflammatory endothelial damage with a superimposed thrombotic late complication and not to recurrent thromboembolism from peripheral deep vein thrombosis.
51% of pts showed pulmonary vascular thrombosis, with a median time from symptoms of 18 days.
We identified a specific radiological pattern of #COVID19 pneumonia with a unique spatial distribution of pulmonary vascular thrombosis overlapping areas of ground-glass opacities.
How we’ll we manage the first ten #COVID19 patients of 2021 (if any) hospitalized for #ARDS (compared to the first 10 patients we managed in February 2020). A multidisciplinary brain storming after managing approx 1000 such patients within the end of Apr 2020. A thread 1/ #FOAMed
2/ Not all our clinical impressions have already published evidence (but the majority was published), but our hospital #COVID19 mortality went close to zero in late April 2020 and we hope medical management accounts for at least part of these results.