Anastasia Troia

Dr. Anastasia Troia

University of Ferrara, Ferrara, Emilia-Romagna, Italy
orcid

Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

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

Representative Publications

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13 July 2024 in Vaccines
Verified
Journal Article
Open access
PDF file
MFMaria Elena Flacco
Maria Elena Flacco
ABAlessandro Bianconi
Alessandro Bianconi
GCGiovanni Cioni
Giovanni Cioni
MFMatteo Fiore
Matteo Fiore
GCGiovanna Letizia Calò
Giovanna Letizia Calò
Lamberto ManzoliLamberto Manzoli
Lamberto Manzoli
The TAK-003 dengue vaccine was licensed in Europe in December 2022, and the official recommendations from most EU countries are still under formulation. To support policymakers, we performed a meta-analysis to quantify TAK-003’s immunogenicity, efficacy and safety among seronegative and seropositive populations after the administration of one or two vaccine doses. We included trials retrieved from MEDLINE, Scopus and ClinicalTrials.gov. The outcomes were the rates of seroconversion, virologically confirmed dengue fever and serious adverse events after each vaccine dose. Data were combined using random-effect proportion or head-to-head meta-analyses. We retrieved a total of 19 datasets, including >20,000 participants. TAK-003 showed an excellent safety profile, and the immunogenicity after two doses against the four DENV serotypes was ≥90% among both adults and children/adolescents who were either seronegative or seropositive at baseline. A single dose was able to elicit a high immunogenic response among adults (≥70%) and children/adolescents (≥90%). The primary two-dose immunization course halved the risk of all types of virologically confirmed dengue fever among seropositive children/adolescents, but seronegative minors were only protected against the diseases caused by DENV-1 and DENV-2. Overall, the results support the use of TAK-003 for the prevention of dengue fever in the pediatric population of endemic countries. Uncertainties remain on the use of a single vaccine dose in non-endemic countries.

27 August 2024 in Vaccines
Verified
Journal Article
Open access
PDF file
ARAnnalisa Rosso
Annalisa Rosso
MFMaria Elena Flacco
Maria Elena Flacco
GCGiovanni Cioni
Giovanni Cioni
MTMarco Tiseo
Marco Tiseo
GIGianmarco Imperiali
Gianmarco Imperiali
Lamberto ManzoliLamberto Manzoli
Lamberto Manzoli
Several vaccines against chikungunya fever have been developed and tested, and one has been recently licensed. We performed a meta-analysis to estimate the immunogenicity and safety of all chikungunya vaccines that have been progressed to clinical trial evaluation (VLA1553; mRNA-1388/VAL-181388; PXVX0317/VRC-CHKVLP059-00-VP; ChAdOx1 Chik; MV-CHIK). We included trials retrieved from MedLine, Scopus, and ClinicalTrials.gov. The outcomes were the rates of seroconversion/seroresponse and serious adverse events (SAEs) after the primary immunization course. We retrieved a total of 14 datasets, including >4000 participants. All candidate chikungunya vaccines were able to elicit an immunogenic response in ≥96% of vaccinated subjects, regardless of the vaccination schedule and platform used, and the seroconversion/seroresponse rates remained high 6 to 12 months after vaccination for most vaccines. Four of the five candidate vaccines showed a good overall safety profile (no data were available for ChAdOx1 Chik), with no significant increase in the risk of SAEs among the vaccinated, and a low absolute risk of product-related SAEs. Overall, the present findings support the potential use of the candidate vaccines for the prevention of chikungunya and the current indication for use in adult travelers to endemic regions of the licensed VLA 1553 vaccine. In order to extend chikungunya vaccination to a wider audience, further studies are needed on individuals from endemic countries and frail populations.

15 October 2024 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
ABAlessandro Bianconi
Alessandro Bianconi
MFMatteo Fiore
Matteo Fiore
ARAnnalisa Rosso
Annalisa Rosso
CMCecilia Acuti Martellucci
Cecilia Acuti Martellucci
GCGiovanna Letizia Calò
Giovanna Letizia Calò
EZEnrico Zauli
Enrico Zauli
Background: Despite the fact that thiocolchicoside has been widely used in the treatment of musculoskeletal pain, its efficacy has never been systematically evaluated. We carried out a systematic review and meta-analysis of randomized clinical trials (RCTs) to appraise the existing evidence on the efficacy of thiocolchicoside for musculoskeletal pain management. Methods: The literature search was performed on multiple databases, extracting reports of RCTs evaluating the efficacy of thiocolchicoside compared to placebo or no exposure. The reduction in pain intensity was evaluated through between-groups mean differences (MDs) in Visual Analogue Scale (VAS) scores after the intervention. The pooled effect estimates were compared to a minimally important difference (MID) of 1 point on a scale from 0 to 10. Results: We retrieved eight RCTs, including a total of 1397 patients. All the included studies were determined as being at high risk of bias. Seven trials evaluated patients with acute low back pain. After 2–3 days of treatment, the pooled MD in VAS score was −0.49 (95%CI = −0.90; −0.09) compared to controls. After 5–7 days of treatment, the summary MD was −0.82 (95%CI = −1.46; −0.18). Conclusions: Although thiocolchicoside was found to significantly reduce patient-reported low back pain, the clinical impact was very small, as the pooled effect estimates were below the MID, and the overall certainty of evidence was very low. In light of the safety concerns raised by the European Medicine Agency, an in-depth analysis on the risk–benefit balance of thiocolchicoside is required.

31 March 2024
Verified
Journal Article
Open access
EGElisa Gabrielli
Elisa Gabrielli
ISIrene Schenone
Irene Schenone
ACAlessandro Roberto Cornio
Alessandro Roberto Cornio
ACAmbrogio Cerri
Ambrogio Cerri
MPMarcello DI Pumpo
Marcello DI Pumpo
GSGiorgio Sessa
Giorgio Sessa
The Health District (HD) is a critical component of Italy’s National Health Service, responsible for ensuring Primary Health Care (PHC) services in response to community health needs. The Italian government established a national strategic reform program, the National Recovery and Resilience Plan (PNRR), starting in 2022, with a series of health interventions to reorganize the PHC setting, the main reform being the Ministerial Decree 77/2022 (DM77). Our study aimed to provide a description of socio-demographic data and to assess the correlation between HDs, in order to suggest health intervention priorities in PHC reforms. We conducted our analysis using a cross-sectional record linkage of data from multiple sources to compare organizational and socio-demographic variables. A dataset was created with each of the 21 Italian Regions’ HDs data of population, land area, mean age, ageing index, old-age dependency ratio, birth rate and death rate. The Inland Areas Project data was integrated for a socio-economic perspective. Our study identified comparable groups of HDs, considering demographical, socio-economic and geographical aspects. The study provides a baseline understanding of the Italian situation prior to the implementation of DM77. It also highlights that inhabitants number cannot be the only variable to take into account for the definition of Italian HDs organisation and PHC reform, providing intercorrelated variables that take into account geographic location, demographic data, and socio-economic aspects. By acknowledging the interplay of demographic, socio-economic, and geographic factors, policymakers can tailor interventions to address diverse community needs, ensuring a more effective and equitable PHC system.

1 April 2024 in Recenti Progressi in Medicina
Verified
Journal Article
Closed access
ACAlessandro Roberto Cornio
Alessandro Roberto Cornio
ESElena Sciurpa
Elena Sciurpa
WPWalter Priano
Walter Priano
Dario GenoveseDario Genovese
Dario Genovese
ACAmbrogio Cerri
Ambrogio Cerri
GSGiorgio Sessa
Giorgio Sessa
Summary. Investing in Primary Health Care (PHC) is crucial for the future of Public Health (PH), although recent studies highlighted the lack of training in PHC within Italian Residency Schools. This article intends to show the experience and impact of a training course focused on standardizing the knowledge of medical residents in Hygiene and preventive medicine regarding PHC. The strength of the intervention was to demonstrate the feasibility of a unique and homogeneous educational path throughout the national territory. From the results of the evaluation questionnaires, a strong approval of the training experience emerged, with a significant improvement in the perceived knowledge of the subject.

1 January 2026 in Journal of Tropical Medicine
Verified
Journal Article
Open access
ATAnastasia Troia
Anastasia Troia
ARAnnalisa Rosso
Annalisa Rosso
GCGiovanni Cioni
Giovanni Cioni
GCGiovanna Letizia Calò
Giovanna Letizia Calò
Lamberto ManzoliLamberto Manzoli
Lamberto Manzoli
MFMaria Elena Flacco
Maria Elena Flacco
Malaria is the most prevalent vector‐borne disease worldwide, with Uganda ranking third for malaria burden in 2023. In resource‐limited settings, where access to diagnosis and treatment is often constrained and recent vaccination strategies may face challenges, traditional primary prevention remains essential and cost‐effective. This study evaluated the effectiveness of the smart home model—an integrated malaria prevention strategy promoted by the Uganda Ministry of Health—in reducing infections among children aged < 5 years. A case–control study was conducted in Oyam District, Northern Uganda, between October 2023 and February 2024. Data from 3093 households were analyzed. Malaria status was assessed using rapid diagnostic tests. Household adherence to nine vector‐control measures defined the smart home score, categorized as low (0–3), intermediate (4–6), or high (7–9). Higher scores were significantly associated with lower malaria prevalence. An inverse association emerged between household score and infection status: households with scores ≥ 7 were associated with a 80% lower presence of infection, as compared to households with scores ≤ 3 (AOR: 0.21; 95% CI: 0.16–0.27). The most protective measures included consistent use of bed nets, closing windows and doors by 6 p.m., eliminating water reservoirs, adopting proper farming practices, and compound cleanliness. These findings may provide further evidence supporting integrated malaria control strategies, alongside vaccines deployment, particularly in low‐resource settings.