Luigi Tritapepe

Prof. Luigi Tritapepe

1. Anesthesia and Intensive Care, Sapienza University of Rome, Circonvallazione Gianicolense 87, 00152 Rome, Italy
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orcid

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 October 2013 in JAMA
Verified
Journal Article
Open access
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AMAndrea Morelli
Andrea Morelli
CEChristian Ertmer
Christian Ertmer
MWMartin Westphal
Martin Westphal
SRSebastian Rehberg
Sebastian Rehberg
TKTim Kampmeier
Tim Kampmeier
MSMervyn Singer
Mervyn Singer
Research from JAMA — Effect of Heart Rate Control With Esmolol on Hemodynamic and Clinical Outcomes in Patients With Septic Shock — A Randomized Clinical Trial

7 April 2020 in World Journal of Emergency Surgery
Verified
Journal Article
Open access
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ACand Federico Coccolini
and Federico Coccolini
Gennaro PerroneGennaro Perrone
Gennaro Perrone
MCMassimo Chiarugi
Massimo Chiarugi
FMFrancesco Di Marzo
Francesco Di Marzo
LALuca Ansaloni
Luca Ansaloni
Fausto CatenaFausto Catena
Fausto Catena
The current COVID-19 pandemic underlines the importance of a mindful utilization of financial and human resources. Preserving resources and manpower is paramount in healthcare. It is important to ensure the ability of surgeons and specialized professionals to function through the pandemic. A conscious effort should be made to minimize infection in this sector. A high mortality rate within this group would be detrimental.This manuscript is the result of a collaboration between the major Italian surgical and anesthesiologic societies: ACOI, SIC, SICUT, SICO, SICG, SIFIPAC, SICE, and SIAARTI. We aim to describe recommended clinical pathways for COVID-19-positive patients requiring acute non-deferrable surgical care. All hospitals should organize dedicated protocols and workforce training as part of the effort to face the current pandemic.

1 August 2007 in Journal of Cardiothoracic and Vascular Anesthesia
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Journal Article
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GLGiovanni Landoni
Giovanni Landoni
Giuseppe Biondi-ZoccaiGiuseppe Biondi-Zoccai
Giuseppe Biondi-Zoccai
AZAlberto Zangrillo
Alberto Zangrillo
EBElena Bignami
Elena Bignami
SDStefania D’aVolio
Stefania D’aVolio
GTGiorgio Torri
Giorgio Torri

1 September 2006 in Critical Care Medicine
Verified
Journal Article
Closed access
AMAndrea Morelli
Andrea Morelli
JTJean Louis Teboul
Jean Louis Teboul
SMSalvatore Maurizio Maggiore
Salvatore Maurizio Maggiore
AVAntoine Vieillard-Baron
Antoine Vieillard-Baron
Monica RoccoMonica Rocco
Monica Rocco
MWMartin Westphal
Martin Westphal
Acute respiratory distress syndrome (ARDS) is frequently associated with increased pulmonary vascular resistance and thus with systolic load of the right ventricle. We hypothesized that levosimendan, a new calcium sensitizer with potential pulmonary vasodilator properties, improves hemodynamics by unloading the right ventricle in patients with ARDS. Prospective, randomized, placebo-controlled, pilot study. Twenty-two-bed multidisciplinary intensive care unit of a university hospital. Thirty-five patients with ARDS in association with septic shock. Patients were randomly allocated to receive a 24-hr infusion of either levosimendan 0.2 μg/kg/min (n = 18) or placebo (n = 17). Data from right heart catheterization, cardiac magnetic resonance, arterial and mixed venous oxygen tensions and saturations, and carbon dioxide tensions were obtained before and 24 hrs after drug infusion. At a mean arterial pressure between 70 and 80 mm Hg (sustained with norepinephrine infusion), levosimendan increased cardiac index (from 3.8 ± 1.1 to 4.2 ± 1.0 L/min/m2) and decreased mean pulmonary artery pressure (from 29 ± 3 to 25 ± 3 mm Hg) and pulmonary vascular resistance index (from 290 ± 77 to 213 ± 50 dynes/s/cm5/m2; each p < .05). Levosimendan also decreased right ventricular end-systolic volume and increased right ventricular ejection fraction (p < .05). In addition, levosimendan increased mixed venous oxygen saturation (from 63 ± 8 to 70 ± 8%; p < .01). This study provides evidence that levosimendan improves right ventricular performance through pulmonary vasodilator effects in septic patients with ARDS. A large multiple-center trial is needed to investigate whether levosimendan is able to improve the overall prognosis of patients with sepsis and ARDS.

23 September 2010 in Annals of Medicine
Verified
Journal Article
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FPFlavia Del Porto
Flavia Del Porto
MPMaria Proietta
Maria Proietta
Luigi TritapepeLuigi Tritapepe
Luigi Tritapepe
FMFabio Miraldi
Fabio Miraldi
AKAngela Koverech
Angela Koverech
GAGiuseppe Aliberti
Giuseppe Aliberti
Objective. The aim of our study was to evaluate the lymphocyte subpopulations and the cytokines in the peripheral blood of patients with type-A Stanford acute aortic dissection (AAD group) and to determine whether inflammatory cells are present at the site of aortic dissection. Methods. Thirty-five consecutive patients with type-A Stanford dissection were evaluated for haemochrome and lymphocyte subpopulations (CD3+, CD4+, CD8+, CD19+, CD4+CD25+, CD16+CD56+, CD4+CD28−, CD8+CD28−) by flow cytometry. C-reactive protein (CRP), tumour necrosis factor (TNF)-α, interleukin (IL)-2, IL-4, IL-6, IL-8, IL-10, interferon-gamma (IFN-γ), and monocyte chemoattractant protein (MCP)-1 were measured by ELISA. In addition, immunohistochemical staining with cell type-specific antibodies was performed to study the inflammatory cells detected inside the aortic wall. Results. In the AAD group, a significant increase in natural killer (NK) (P = 0.032), B cells (P = 0.022), and CD8+CD28− (P = 0.045) subpopulations was observed, whereas there was a significant decrease in total T lymphocytes (P = 0.004) and T helper fractions (P = 0.005). Moreover, a significant increase in CRP (P < 0.0001), IL-6 (P < 0.0001), IL-8 (P < 0.0001), IL-10 (P < 0.0001), TNF-α (P < 0.0001), and MCP-1 (P < 0.001) was observed; macrophages represented the main population detected inside the media. Conclusions. Our results strongly support the hypothesis of a pivotal role of innate immunity in type-A Stanford AAD.

4 August 2018 in Critical Care
Verified
Journal Article
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Filippo SanfilippoFilippo Sanfilippo
Filippo Sanfilippo
CCC. Corredor
C. Corredor
NFN. Fletcher
N. Fletcher
Luigi TritapepeLuigi Tritapepe
Luigi Tritapepe
FLF. L. Lorini
F. L. Lorini
MCM. Cecconi
M. Cecconi
Sepsis-induced myocardial dysfunction is associated with poor outcomes, but traditional measurements of systolic function such as left ventricular ejection fraction (LVEF) do not directly correlate with prognosis. Global longitudinal strain (GLS) utilizing speckle-tracking echocardiography (STE) could be a better marker of intrinsic left ventricular (LV) function, reflecting myocardial deformation rather than displacement and volume changes. We sought to investigate the prognostic value of GLS in patients with sepsis and/or septic shock. We conducted a systematic review (PubMed and Embase up to 26 October 2017) and meta-analysis to investigate the association between GLS and mortality at longest follow up in patients with severe sepsis and/or septic shock. In the primary analysis, we included studies reporting transthoracic echocardiography data on GLS according to mortality. A secondary analysis evaluated the association between LVEF and mortality including data from studies reporting GLS. We included eight studies in the primary analysis with a total of 794 patients (survival 68%, n = 540). We found a significant association between worse LV function and GLS values and mortality: standard mean difference (SMD) − 0.26; 95% confidence interval (CI) − 0.47, − 0.04; p = 0.02 (low heterogeneity, I2 = 43%). No significant association was found between LVEF and mortality in the same population of patients (eight studies; SMD, 0.02; 95% CI − 0.14, 0.17; p = 0.83; no heterogeneity, I2 = 3%). Worse GLS (less negative) values are associated with higher mortality in patients with severe sepsis or septic shock, while such association is not valid for LVEF. More critical care research is warranted to confirm the better ability of STE in demonstrating underlying intrinsic myocardial disease compared to LVEF.