Marina Pieri

Dr. Marina Pieri


Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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13 July 2020 in Blood Purification
Verified
Journal Article
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EFEvgeny Fominskiy
Evgeny Fominskiy
ASAnna Mara Scandroglio
Anna Mara Scandroglio
GMGiacomo Monti
Giacomo Monti
MCMaria Grazia Calabrò
Maria Grazia Calabrò
GLGiovanni Landoni
Giovanni Landoni
FGfor the COVID-BioB Study Group
for the COVID-BioB Study Group
Background: There is no information on acute kidney injury (AKI) and continuous renal replacement therapy (CRRT) among invasively ventilated coronavirus disease 2019 (COVID-19) patients in Western healthcare systems. Objective: To study the prevalence, characteristics, risk factors and outcome of AKI and CRRT among invasively ventilated COVID-19 patients. Methods: Observational study in a tertiary care hospital in Milan, Italy. Results: Among 99 patients, 72 (75.0%) developed AKI and 17 (17.7%) received CRRT. Most of the patients developed stage 1 AKI (33 [45.8%]), while 15 (20.8%) developed stage 2 AKI and 24 (33.4%) a stage 3 AKI. Patients who developed AKI or needed CRRT at latest follow-up were older, and among CRRT treated patients a greater proportion had preexisting CKD. Hospital mortality was 38.9% for AKI and 52.9% for CRRT patients. Conclusions: Among invasively ventilated COVID-19 patients, AKI is very common and CRRT use is common. Both carry a high risk of in-hospital mortality.

6 February 2025 in British Journal of Anaesthesia
Verified
Journal Article
Closed access
FDFilippo D'Amico
Filippo D'Amico
SDSara Dormio
Sara Dormio
GVGiulia Veronesi
Giulia Veronesi
FGFabio Guarracino
Fabio Guarracino
KDKatia Donadello
Katia Donadello
PGPREHAB study group
PREHAB study group

14 October 2015 in BMC Cardiovascular Disorders
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Journal Article
Open access
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MPMarina Pieri
Marina Pieri
RCRachele Contri
Rachele Contri
DWDario Winterton
Dario Winterton
MMMatteo Montorfano
Matteo Montorfano
ACAntonio Colombo
Antonio Colombo
Federico PappalardoFederico Pappalardo
Federico Pappalardo
The treatment of cardiogenic shock with percutaneous mechanical circulatory support (MCS) is attractive: however, at present it is not clear which is the best strategy, as no survival benefit has been demonstrated for any device as single therapy. Aim of this study is to describe the role of percutaneous Impella in a comprehensive MCS program. Observational study on 22 patients supported with the Impella device in our hospital from May 2013 to June 2014. Four patients (18 %) were treated with Impella alone, 8 patients (36 %) were treated with Impella and IABP, 6 patients (27 %) with Impella and VA ECMO, and 4 patients (18 %) with Impella, IABP and VA ECMO. The cause of cardiogenic shock was myocardial infarction (CSMI) in 9 patients (41 %), postcardiotomic cardiogenic shock in 5 (23 %), and a miscellaneous of other causes in the remaining 8 (36 %). Eight Impella devices (36 %) were placed under transesophageal echocardiographic guidance, while 14 (64 %) under fluoroscopy. The device was removed with manual compression at bedside and no vascular complications were observed. Duration of Impella support was 107 (54–141) hours and duration of ventilation was 48 (14–92) hours. Hemolysis occurred in 6 patients (27 %), while major bleeding in 4 patients (18 %). Survival was 73 %: 13 patients (58 %) showed recovery of cardiac function; 1 patient (5 %) was bridged to left ventricular assist device (LVAD) implantation, 1 patient (5 %) to heart transplantation (HTx) and 1 patient (5 %) received a BiVAD and was eventually bridged to HTx. Our data suggest that a multi-device approach, encompassing active LV support with Impella, is safe and can significantly improve survival in patients with cardiogenic shock.

20 October 2016 in Journal of Cardiac Surgery
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Journal Article
Closed access
PDF file
MPMarina Pieri
Marina Pieri
ASAnna Mara Scandroglio
Anna Mara Scandroglio
MMMarcus Müller
Marcus Müller
PPPanagiotis Pergantis
Panagiotis Pergantis
AKAlexandra Kretzschmar
Alexandra Kretzschmar
MKMarian Kukucka
Marian Kukucka
Driveline infections in patients with implantable left ventricular assist devices (VAD) carry increasing risk for pump infection, thromboembolic events, decreased quality of life, and increased hospitalization. We report our experience with a surgical technique for refractory driveline infections without mediastinitis consisting of translocation and wrapping of the driveline with greater omentum tissue. We retrospectively reviewed data of VAD patients who underwent surgical treatment by translocation and wrapping with omentum for severe chronic driveline infection. Thirteen patients were treated between January 2010 and October 2015; 12 (92%) were male, and the mean age was 56 ± 14 years. Ten patients (77%) were managed with driveline sheathing with omentum and repositioning with a new exit site, and three (23%), suffering from driveline fistula, with driveline covering with omentum maintaining the previous exit site. Three episodes of postoperative bleeding (23%) required surgical revision. Twelve patients (92%) were discharged from the hospital and one (8%) died. Nine patients (69%) were free from infection at the time of discharge, and three (23%) had recurrence of infection within the first postoperative year. Only four patients (31%) required admission to the intensive care unit; overall median hospital stay was 23 days (range 7-205 days). Driveline relocation with use of omentum is a feasible and effective procedure in selected cases of chronic severe driveline infection. The risk for perioperative bleeding should be taken into consideration and carefully monitored.

11 April 2024 in Resuscitation
Verified
Journal Article
Closed access
MBMatteo Aldo Bonizzoni
Matteo Aldo Bonizzoni
TSTommaso Scquizzato
Tommaso Scquizzato
MPMarina Pieri
Marina Pieri
SDSilvia Delrio
Silvia Delrio
PNPasquale Nardelli
Pasquale Nardelli
TSTommaso Scaglia
Tommaso Scaglia

23 May 2024 in ESC Heart Failure
Verified
Journal Article
Open access
FCFilippo Consolo
Filippo Consolo
JUJacopo D'ANdria Ursoleo
Jacopo D'ANdria Ursoleo
MPMarina Pieri
Marina Pieri
PNPasquale Nardelli
Pasquale Nardelli
LCLorenzo Cianfanelli
Lorenzo Cianfanelli
ASAnna Mara Scandroglio
Anna Mara Scandroglio
Aims: Artificial intelligence (AI) has emerged as a potential useful tool to support clinical treatment of heart failure, including the setting of mechanical circulatory support (MCS). Modern Impella pumps are equipped with advanced technology (SmartAssist), enabling real-time acquisition and display of data related to both pump performance and the patient's haemodynamic status. These data emerge as an ‘ideal’ source for data-driven AI applications to predict the clinical course of an ongoing therapeutic protocol. Yet, no evidence of effective application of AI tools in the setting of Impella support is available. On this background, we aimed at identifying possible future applications of AI-based tools in the setting of temporary MCS with an Impella device. Methods: We explored the state of research and development at the intersection of AI and Impella support and derived future potential applications of AI in routine Impella clinical management. Results: We identified different areas where the future implementation of AI tools may contribute to addressing important clinical challenges in the setting of Impella support, including (i) early identification of the best suited pathway of care according to patients' conditions at presentation and intention to treat, (ii) prediction of therapy outcomes according to different possible therapeutic actions, (iii) optimization of device implantation procedures and evaluation of proper pump position over the whole course of support and (iv) prevention and/or rationale management of haemocompatibility-related adverse events. For each of those areas, we discuss the potential advantages, challenges and implications of harnessing AI-driven insights in the setting of MCS with an Impella device. Conclusions: Temporary MCS with an Impella device has great potential to benefit from the integration of AI-based tools. Such tools may indeed translate into groundbreaking innovation supporting clinical decision-making and therapy regulation, in particular in complex scenarios such as the multidevice MCS strategy.