Patient population and study design

DR Daniele Ronco
MM Matteo Matteucci
JR Justine Mafalda Ravaux
MK Mariusz Kowalewski
GM Giulio Massimi
FT Federica Torchio
CT Cinzia Trumello
SN Shiho Naito
NB Nikolaos Bonaros
MB Michele De Bonis
DF Dario Fina
AK Adam Kowalówka
MD Marek Deja
FJ Federica Jiritano
GS Giuseppe Filiberto Serraino
JK Jurij Matija Kalisnik
CV Carlo De Vincentiis
MR Marco Ranucci
TF Theodor Fischlein
CR Claudio Francesco Russo
MC Massimiliano Carrozzini
UB Udo Boeken
NK Nikolaos Kalampokas
MG Michele Golino
RP Roberto De Ponti
MP Matteo Pozzi
JO Jean-François Obadia
MT Matthias Thielmann
RS Roberto Scrofani
SB Stefania Blasi
GT Giovanni Troise
CA Carlo Antona
AM Andrea De Martino
GF Giosuè Falcetta
GD Guglielmo Actis Dato
PS Paolo Severgnini
AM Andrea Musazzi
RL Roberto Lorusso
request Request a Protocol
ask Ask a question
Favorite

The patients were recruited from the database of the CAUTION-COVID19 study (‘Mechanical complications of acute myocardial infarction: an international multicentre cohort study during COVID-19 pandemic among hospitalized patients’). The CAUTION-COVID19 study (trial registration: Clinicaltrials.gov, NCT04813692) is a retrospective, multicentre, observational trial aimed at evaluating the incidence, treatment and outcomes of post-AMI MCs during the first year of the COVID-19 pandemic with respect to the 2 previous years. The herein reported study included all the adult patients (aged >18 years) who were hospitalized with a diagnosis of post-AMI MCs, independently of the treatment received (i.e. surgical, percutaneous or conservative), between 1 March 2018 and 28 February 2021 in 18 different centres from 6 European countries (Austria, France, Germany, Italy, Poland and the Netherlands), as presented in Fig. 1. Patients have been identified through diagnosis-specific ICD-9 codes, administrative databases or surgical records.

Distribution of European centres enrolled in the study.

The study was conducted in accordance with the guidelines of the Declaration of Helsinki for patient data use and evaluation. A unified patient dataset was used to collect pertinent information, including demographic characteristics, clinical history, diagnostic workup, type of treatment and operative and postoperative data, as well as information on outcomes, from medical records. This report follows the STROBE reporting guidelines for observational studies.

Do you have any questions about this protocol?

Post your question to gather feedback from the community. We will also invite the authors of this article to respond.

0/150

tip Tips for asking effective questions

+ Description

Write a detailed description. Include all information that will help others answer your question including experimental processes, conditions, and relevant images.

post Post a Question
0 Q&A