Alessio Strazzulla

Dr. Alessio Strazzulla


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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18 June 2013 in BioMed Research International
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Journal Article
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ASAlessio Strazzulla
Alessio Strazzulla
Salvatore CocuzzaSalvatore Cocuzza
Salvatore Cocuzza
MPMarilia Rita Pinzone
Marilia Rita Pinzone
MPMaria Concetta Postorino
Maria Concetta Postorino
SCStefano Cosentino
Stefano Cosentino
GNGiuseppe Nunnari
Giuseppe Nunnari
We present a review of current knowledge about mucosal leishmaniasis (ML). Although involvement of mucous membranes is classically admitted in New World leishmaniasis, particularly occurring in infection byLeishmania (L.) braziliensisspecies complex, ML is also a possible presentation of Old World leishmaniasis, in eitherL. donovaniorL. majorspecies complex infections. Thus, ML has to be considered not only as a Latin American disease but as an Old and New World disease. We describe ML epidemiology, pathogenesis, clinics, diagnosis, and therapy. Considering both its highly disfiguring lesions and its possible lethal outcome, ML should not be underestimated by physicians. Moreover, leishmaniasis is expected to increase its burden in many countries as sandfly vector distribution is widespreading towards non-endemic areas. Finally, the lack of clear understanding of ML pathogenesis and the absence of effective human vaccines strongly claim for more research.

16 August 2021 in Antibiotics
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MRMaxence ROUYER
Maxence ROUYER
ASAlessio Strazzulla
Alessio Strazzulla
TYTracie Joyner Youbong
Tracie Joyner Youbong
PTPaul Tarteret
Paul Tarteret
APAurélia Pitsch
Aurélia Pitsch
SDSylvain Diamantis
Sylvain Diamantis
Introduction: Aim of this study is to analyse the characteristics of ventilator-associated pneumonia (VAP) inpatients infected by severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2). Materials and Methods: A retrospective study was conducted, including coronavirus infectious disease 2019 (COVID-19) patients who developed VAP from March to May 2020 (VAP COVID-19). They were compared to non-COVID-19 patients who developed VAP from January 2011 to December 2019 (VAP NO COVID-19) and COVID-19 patients who did not develop VAP (NO VAP COVID-19). Results: Overall, 42 patients were included in the VAP COVID-19group, 37 in the NO VAP COVID-19 group, and 188 in the VAP NO COVID-19 group. VAP COVID-19 had significantly higher rates of shock (71% vs. 48%, p = 0.009), death in ICU (52% vs. 30%, p = 0.011), VAP recurrence (28% vs. 4%, p < 0.0001), positive blood culture (26% vs. 13%, p = 0.038), and polymicrobial culture (28% vs. 13%, p = 0.011) than VAP NO COVID-19. At the multivariate analysis, death in patients with VAP was associated with shock (p = 0.032) and SARS-CoV-2 (p = 0.008) infection. Conclusions: VAP in COVID-19 patients is associated with shock, bloodstream, and polymicrobial infections.

Verified
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Nadia MarascioNadia Marascio
Nadia Marascio
GPGrazia Pavia
Grazia Pavia
ASAlessio Strazzulla
Alessio Strazzulla
TDTim Dierckx
Tim Dierckx
LCLize Cuypers
Lize Cuypers
TGThe SINERGIE-UMG Study Group
The SINERGIE-UMG Study Group
Naturally occurring resistance-associated substitutions (RASs) can negatively impact the response to direct-acting antivirals (DAAs) agents-based therapies for hepatitis C virus (HCV) infection. Herein, we set out to characterize the RASs in the HCV1b genome from serum samples of DAA-naïve patients in the context of the SINERGIE (South Italian Network for Rational Guidelines and International Epidemiology, 2014) project. We deep-sequenced the NS3/4A protease region of the viral population using the Ion Torrent Personal Genome Machine, and patient-specific majority rule consensus sequence summaries were constructed with a combination of freely available next generation sequencing data analysis software. We detected NS3/4A protease major and minor variants associated with resistance to boceprevir (V36L), telaprevir (V36L, I132V), simeprevir (V36L), and grazoprevir (V36L, V170I). Furthermore, we sequenced part of HCV NS5B polymerase using Sanger-sequencing and detected a natural RAS for dasabuvir (C316N). This mutation could be important for treatment strategies in cases of previous therapy failure.

16 October 2018 in BMC Infectious Diseases
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Journal Article
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TGthe CARDIAC study group
the CARDIAC study group
MMMaria Mazzitelli
Maria Mazzitelli
CTCarlo Torti
Carlo Torti
JSJolanda Sabatino
Jolanda Sabatino
GDGreta Luana D'Ascoli
Greta Luana D'Ascoli
CICiro Indolfi
Ciro Indolfi
Possible cardiotoxicity of sofosbuvir in humans has not been demonstrated yet. Also, since HCV can exert deleterious effects on hearth function, it is of interest to know whether HCV eradication provides any benefits using global longitudinal strain (GLS), a measure of left ventricular function more reliable than ejection fraction (EF). Patients eligible for treatment with the combination therapy for HCV were invited to perform a transthoracic cardiac ultrasound at four different time points: before starting treatment, after one month, at the end of treatment and, after six month. Left ventricular function was measured with both EF and GLS. From March 2015 to December 2016, 82 patients were enrolled. Fifty-six percent patients were males. Mean age was 66.12 (SD: 9.25) years. About 20% patients did not present any cardiovascular risk factors or comorbidities. A worsening trend of GLS was observed. Variations were not found to be statistically significant when EF was studied along the follow-up. However, when GLS was studied, its variations were found to be statistically significant indicating a worsening effect, albeit with different trends in patients who underwent treatment for three months compared to six months. Worsening of GLS was found to be statistically significant even after adjusting for body mass index and liver fibrosis, independently from treatment duration. Our results showed unexpected worsening of left ventricular function when measured through GLS after HCV treatment response induced by DAAs including sofosbuvir. Although this result is not proven to be clinically significant, the safety profile of sofosbuvir-based regimens needs to be studied further.

31 July 2017 in Infectious Diseases in Obstetrics and Gynecology
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MMMaria Mazzitelli
Maria Mazzitelli
MMMariella Micieli
Mariella Micieli
CVCarmela Votino
Carmela Votino
FVFederica Visconti
Federica Visconti
PQPaola Quaresima
Paola Quaresima
FZFulvio Zullo
Fulvio Zullo
Currently, the only efficient way to prevent human Cytomegalovirus (HCMV) infection in pregnancy is primary prophylaxis through hygienic measures. So, we evaluated knowledge of HCMV and its prevention in a group of pregnant women. An anonymous questionnaire with multiple-choice answers was administered to all pregnant women who were followed up at the Obstetrics and Gynecology Unit of “Pugliese-Ciaccio Hospital,” a third-level hospital in Catanzaro (Southern Italy), from November 2015 to March 2016. Previously prescribed serology results for HCMV were also evaluated. Three hundred and fifty women participated in the study and the results clearly demonstrated that knowledge of pregnant women about HCMV is poor. Moreover, prescribed screening procedures need to be optimized, since one out of three pregnant women has not been tested for HCMV or the screening was not performed adequately. For this reason, it is important to implement informative campaign in both pregnant women and providing physicians.

1 September 2015
Verified
Journal Article
Closed access
ASAlessio Strazzulla
Alessio Strazzulla
GBGiorgio Settimo Barreca
Giorgio Settimo Barreca
AGAida Giancotti
Aida Giancotti
VPVincenzo Pisani
Vincenzo Pisani
CCChiara Costa
Chiara Costa
CTCarlo Torti
Carlo Torti