95 results on '"Campoli, C."'
Search Results
2. Serum bactericidal titres for monitoring antimicrobial therapy: current status and potential role in the management of multidrug-resistant Gram-negative infections
- Author
-
Zaghi, I., Gaibani, P., Campoli, C., Bartoletti, M., Giannella, M., Ambretti, S., Viale, P., and Lewis, R.E.
- Published
- 2020
- Full Text
- View/download PDF
3. The impact of carbapenemase-producing Enterobacteriaceae colonization on infection risk after liver transplantation: a prospective observational cohort study
- Author
-
Giannella, M., Bartoletti, M., Campoli, C., Rinaldi, M., Coladonato, S., Pascale, R., Tedeschi, S., Ambretti, S., Cristini, F., Tumietto, F., Siniscalchi, A., Bertuzzo, V., Morelli, M.C., Cescon, M., Pinna, A.D., Lewis, R., and Viale, P.
- Published
- 2019
- Full Text
- View/download PDF
4. Corrigendum to: “Development and validation of a prediction model for severe respiratory failure in hospitalized patients with SARS-CoV-2 infection: a multicentre cohort study (PREDI-CO study)” Clinical Microbiology and Infection 26 (2020) 1545–1553 (Clinical Microbiology and Infection (2020) 26(11) (1545–1553), (S1198743X20304791), (10.1016/j.cmi.2020.08.003))
- Author
-
Bartoletti M., Bartoletti, M, Giannella, M, Scudeller, L, Tedeschi, S, Rinaldi, M, Bussini, L, Fornaro, G, Pascale, R, Pancaldi, L, Pasquini, Z, Trapani, F, Badia, L, Campoli, C, Tadolini, M, Attard, L, Puoti, M, Merli, M, Mussini, C, Menozzi, M, Meschiari, M, Codeluppi, M, Barchiesi, F, Cristini, F, Saracino, A, Licci, A, Rapuano, S, Tonetti, T, Gaibani, P, Ranieri, V, Viale, P, Bartoletti M., Giannella M., Scudeller L., Tedeschi S., Rinaldi M., Bussini L., Fornaro G., Pascale R., Pancaldi L., Pasquini Z., Trapani F., Badia L., Campoli C., Tadolini M., Attard L., Puoti M., Merli M., Mussini C., Menozzi M., Meschiari M., Codeluppi M., Barchiesi F., Cristini F., Saracino A., Licci A., Rapuano S., Tonetti T., Gaibani P., Ranieri V. M., Viale P., Bartoletti M., Bartoletti, M, Giannella, M, Scudeller, L, Tedeschi, S, Rinaldi, M, Bussini, L, Fornaro, G, Pascale, R, Pancaldi, L, Pasquini, Z, Trapani, F, Badia, L, Campoli, C, Tadolini, M, Attard, L, Puoti, M, Merli, M, Mussini, C, Menozzi, M, Meschiari, M, Codeluppi, M, Barchiesi, F, Cristini, F, Saracino, A, Licci, A, Rapuano, S, Tonetti, T, Gaibani, P, Ranieri, V, Viale, P, Bartoletti M., Giannella M., Scudeller L., Tedeschi S., Rinaldi M., Bussini L., Fornaro G., Pascale R., Pancaldi L., Pasquini Z., Trapani F., Badia L., Campoli C., Tadolini M., Attard L., Puoti M., Merli M., Mussini C., Menozzi M., Meschiari M., Codeluppi M., Barchiesi F., Cristini F., Saracino A., Licci A., Rapuano S., Tonetti T., Gaibani P., Ranieri V. M., and Viale P.
- Abstract
The authors regret that an author's name which should be on the list of the PREDICO study group was mistakenly listed in the appendix at the end of the article. Further, on Pubmed (https://pubmed.ncbi.nlm.nih.gov/32781244/) the name is wrongly reported as an affiliation (19Lucia Diella Infectious Disease Unit - Department of Biomedical Sciences and Human Oncology, University of Bari, Policlinico di Bari, Italy.) It should be 19Infectious Disease Unit - Department of Biomedical Sciences and Human Oncology, University of Bari, Policlinico di Bari, Italy. This affiliation belongs to Lucia Diella. The authors would like to apologise for any inconvenience caused.
- Published
- 2023
5. Risk Factors for Infection With Carbapenem-Resistant Klebsiella pneumoniae
- Author
-
Giannella, M., Bartoletti, M., Morelli, M.C., Tedeschi, S., Cristini, F., Tumietto, F., Pasqualini, E., Danese, I., Campoli, C., Di Lauria, N., Faenza, S., Ercolani, G., Lewis, R., Pinna, A.D., and Viale, P.
- Published
- 2015
- Full Text
- View/download PDF
6. A prospective multicentre study of the epidemiology and outcomes of bloodstream infection in cirrhotic patients
- Author
-
Campoli, C., Siccardi, G., Ambretti, S., Stallmach, A., Venditti, M., Lucidi, C., Ludovisi, S., De Cueto, M., Navarro, M.D., Lopez Cortes, E., Bouza, E., Valerio, M., Eworo, A., Losito, R., Senzolo, M., Nadal, E., Ottobrelli, A., Varguvic, M., Badia, C., Borgia, G., Gentile, I., Buonomo, A.R., Boumis, E., Beteta-Lopez, A., Rianda, A., Taliani, G., Grieco, S., Bartoletti, M., Giannella, M., Lewis, R., Caraceni, P., Tedeschi, S., Paul, M., Schramm, C., Bruns, T., Merli, M., Cobos-Trigueros, N., Seminari, E., Retamar, P., Muñoz, P., Tumbarello, M., Burra, P., Torrani Cerenzia, M., Barsic, B., Calbo, E., Maraolo, A.E., Petrosillo, N., Galan-Ladero, M.A., D'Offizi, G., Bar Sinai, N., Rodríguez-Baño, J., Verucchi, G., Bernardi, M., and Viale, P.
- Published
- 2018
- Full Text
- View/download PDF
7. High-dose ivermectin for early treatment of COVID-19 (COVER study): a randomised, double-blind, multicentre, phase II, dose-finding, proof-of-concept clinical trial
- Author
-
Buonfrate D, Chesini F, Martini D, Roncaglioni MC, Ojeda Fernandez ML, Alvisi MF, De Simone I, Rulli E, Nobili A, Casalini G, Antinori S, Gobbi M, Campoli C, Deiana M, Pomari E, Lunardi G, Tessari R, and Bisoffi Z
- Subjects
COVID-19 ,Ivermectin ,Randomised controlled trial ,SARS-CoV-2 - Abstract
High concentrations of ivermectin demonstrated antiviral activity against SARS-CoV-2 in vitro. The aim of this study was to assess the safety and efficacy of high-dose ivermectin in reducing viral load in individuals with early SARS-CoV-2 infection. This was a randomised, double-blind, multicentre, phase II, dose-finding, proof-of-concept clinical trial. Participants were adults recently diagnosed with asymptomatic/oligosymptomatic SARS-CoV-2 infection. Exclusion criteria were: pregnant or lactating women; CNS disease; dialysis; severe medical condition with prognosis 10viral load reduction was 2.9 (1.6) in arm C, 2.5 (2.2) in arm B and 2.0 (2.1) in arm A, with no significant differences (P = 0.099 and 0.122 for C vs. A and B vs. A, respectively). High-dose ivermectin was safe but did not show efficacy to reduce viral load. For anonymization purpose, the dates of recruitment have been shifted of an unspecifiednumber of days. However, timeframe between follow up visits remains fixed.
- Published
- 2022
8. Prevalence of Gastrointestinal Symptoms in Severe Acute Respiratory Syndrome Coronavirus 2 Infection: Results of the Prospective Controlled Multinational GI-COVID-19 Study
- Author
-
Marasco, G., Cremon, C., Barbaro, M. R., Salvi, D., Cacciari, G., Kagramanova, A., Bordin, D., Drug, V., Miftode, E., Fusaroli, P., Mohamed, S. Y., Ricci, C., Bellini, M., Rahman, M. M., Melcarne, L., Santos, J., Lobo, B., Bor, S., Yapali, S., Akyol, D., Sapmaz, F. P., Urun, Y. Y., Eskazan, T., Celebi, A., Kacmaz, H., Ebik, B., Binicier, H. C., Bugdayci, M. S., Yagci, M. B., Pullukcu, H., Kaya, B. Y., Tureyen, A., Hatemi, I., Koc, E. S., Sirin, G., Caliskan, A. R., Bengi, G., Alis, E. E., Lukic, S., Trajkovska, M., Hod, K., Dumitrascu, D., Pietrangelo, A., Corradini, E., Simren, M., Sjolund, J., Tornkvist, N., Ghoshal, U. C., Kolokolnikova, O., Colecchia, A., Serra, J., Maconi, G., De Giorgio, R., Danese, S., Portincasa, P., Di Stefano, M., Maggio, M., Philippou, E., Lee, Y. Y., Venturi, A., Borghi, C., Zoli, M., Gionchetti, P., Viale, P., Stanghellini, V., Barbara, G., Piacentini, A., Shengelia, M., Vechorko, V., Cardamone, C., Rosei, C. A., Pancetti, A., Rettura, F., Pedrosa, M., Campoli, C., Mijac, D., Korac, M., Karic, U., Markovic, A., Najdeski, A., Nikolova, D., Dimzova, M., Lior, O., Shinhar, N., Perelmutter, O., Ringel, Y., Sabo, C. M., Chis, A., Bonucchi, G., Caio, G. P. I., Ghirardi, C., Marziani, B., Rizzello, B., Aguilar, A., Capogreco, A., Aghemo, A., Di Paolo, D. M., Marconi, G., Di Sabatino, A., Tagliaferri, S., Naves, J. E., Galli, A., Dragoni, G., Nedelcu, L., Mauloni, P. A., Del Vecchio, S., Rotondo, L., Capuani, F., Montanari, D., Palombo, F., Paone, C., Mastel, G., Fontana, C., Bellacosa, L., Cogliandro, R. F., Marasco, Giovanni, Cremon, Cesare, Barbaro, Maria Raffaella, Salvi, Daniele, Cacciari, Giulia, Kagramanova, Anna, Bordin, Dmitry, Drug, Vasile, Miftode, Edgidia, Fusaroli, Pietro, Mohamed, Salem Youssef, Ricci, Chiara, Bellini, Massimo, Rahman, M Masudur, Melcarne, Luigi, Santos, Javier, Lobo, Beatriz, Bor, Serhat, Yapali, Suna, Akyol, Deniz, Sapmaz, Ferdane Pirincci, Urun, Yonca Yilmaz, Eskazan, Tugce, Celebi, Altay, Kacmaz, Huseyin, Ebik, Berat, Binicier, Hatice Cilem, Bugdayci, Mehmet Sait, Yağcı, Munkhtsetseg Banzragch, Pullukcu, Husnu, Kaya, Berrin Yalınba, Tureyen, Ali, Hatemi, İbrahim, Koc, Elif Sitre, Sirin, Goktug, Calıskan, Ali Riza, Bengi, Goksel, Alıs, Esra Ergun, Lukic, Snezana, Trajkovska, Meri, Hod, Keren, Dumitrascu, Dan, Pietrangelo, Antonello, Corradini, Elena, Simren, Magnu, Sjolund, Jessica, Tornkvist, Navkiran, Ghoshal, Uday C, Kolokolnikova, Olga, Colecchia, Antonio, Serra, Jordi, Maconi, Giovanni, De Giorgio, Roberto, Danese, Silvio, Portincasa, Pietro, Di Stefano, Michele, Maggio, Marcello, Philippou, Elena, Lee, Yeong Yeh, Venturi, Alessandro, Borghi, Claudio, Zoli, Marco, Gionchetti, Paolo, Viale, Pierluigi, Stanghellini, Vincenzo, and Barbara, Giovanni
- Subjects
Male ,medicine.medical_specialty ,Settore MED/17 - Malattie Infettive ,Coronavirus disease 2019 (COVID-19) ,Nausea ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,diarrhea ,Disease ,Gastrointestinal Symptoms, COVID-19, Acute Respiratory Syndrome, GI-COVID-19 ,NO ,Russia ,Manifestations ,Interviews as Topic ,Rating scale ,Internal medicine ,Surveys and Questionnaires ,parasitic diseases ,medicine ,Prevalence ,Humans ,In patient ,Prospective Studies ,Respiratory system ,Settore MED/12 - Gastroenterologia ,Hepatology ,business.industry ,SARS-CoV-2 ,pandemic ,Gastroenterology ,COVID-19 ,Middle Aged ,gastrointestinal ,Gastroenteritis ,Europe ,Hospital admission ,Egypt ,Female ,medicine.symptom ,business ,human activities - Abstract
INTRODUCTION: Gastrointestinal (GI) symptoms in coronavirus-19 disease (COVID-19) have been reported with great variability and without standardization. In hospitalized patients, we aimed to evaluate the prevalence of GI symptoms, factors associated with their occurrence, and variation at 1 month. METHODS: The GI-COVID-19 is a prospective, multicenter, controlled study. Patients with and without COVID-19 diagnosis were recruited at hospital admission and asked for GI symptoms at admission and after 1 month, using the validated Gastrointestinal Symptom Rating Scale questionnaire. RESULTS: The study included 2036 hospitalized patients. A total of 871 patients (575 COVID+ and 296 COVID-) were included for the primary analysis. GI symptoms occurred more frequently in patients with COVID-19 (59.7%; 343/575 patients) than in the control group (43.2%; 128/296 patients) (P < 0.001). Patients with COVID-19 complained of higher presence or intensity of nausea, diarrhea, loose stools, and urgency as compared with controls. At a 1-month follow-up, a reduction in the presence or intensity of GI symptoms was found in COVID-19 patients with GI symptoms at hospital admission. Nausea remained increased over controls. Factors significantly associated with nausea persistence in COVID-19 were female sex, high body mass index, the presence of dyspnea, and increased C-reactive protein levels. DISCUSSION: The prevalence of GI symptoms in hospitalized patients with COVID-19 is higher than previously reported. Systemic and respiratory symptoms are often associated with GI complaints. Nausea may persist after the resolution of COVID-19 infection., Fondazione Cassa di Risparmio in Bologna; Italian Ministry of Education, University and Research; Fondazione del Monte di Bologna e Ravenna [SC1-BHC-01-2019]; European Grant H2020, DISCOvERIE [SC1-BHC-01-2019]; Italian Ministry of Health [Ricerca Finalizzata GR-2018-12367062], G.B. contribution to this research was permitted in part by funding from Fondazione Cassa di Risparmio in Bologna; the ItalianMinistry of Education, University and Research; and Fondazione del Monte di Bologna e Ravenna and European Grant H2020, DISCOvERIE, SC1-BHC-01-2019. M.R.B. is a recipient of a grant from the Italian Ministry of Health (Ricerca Finalizzata GR-2018-12367062). None of the funding organizations have had any role in the design and conduct of the study; in the collection, management, and analysis of the data; or in the preparation, review, and approval of the article.
- Published
- 2022
9. Development of a Risk Prediction Model for Carbapenem-resistant Enterobacteriaceae Infection after Liver Transplantation: A Multinational Cohort Study
- Author
-
Giannella, M., Freire, M., Rinaldi, M., Abdala, E., Rubin, A., Mularoni, A., Gruttadauria, S., Grossi, P., Shbaklo, N., Tandoi, F., Ferrarese, A., Burra, P., Fernandes, R., Aranha Camargo, L. F., Asensio, A., Alagna, L., Bandera, A., Simkins, J., Abbo, L., Halpern, M., Santana Girao, E., Valerio, M., Munoz, P., Fernandez Yunquera, A., Statlender, L., Yahav, D., Franceschini, E., Graziano, E., Morelli, M. C., Cescon, M., Viale, P., Lewis, R., Bartoletti, M., Pascale, R., Campoli, C., Coladonato, S., Cristini, F., Tumietto, F., Siniscalchi, A., Laici, C., Ambretti, S., Romagnoli, R., De Rosa, F. G., Muscatello, A., Mangioni, D., Gori, A., Antonelli, B., Dondossola, D., Rossi, G., Invernizzi, F., Peghin, M., Cillo, U., Mussini, C., Benedetto, F. D., Terrabuio, D. R. B., Bittante, C. D., Toniolo, A. D. R., Balbi, E., Garcia, J. H. P., Morras, I., Ramos, A., Cruz, A. F., Salcedo, M., Giannella M., Freire M., Rinaldi M., Abdala E., Rubin A., Mularoni A., Gruttadauria S., Grossi P., Shbaklo N., Tandoi F., Ferrarese A., Burra P., Fernandes R., Aranha Camargo L.F., Asensio A., Alagna L., Bandera A., Simkins J., Abbo L., Halpern M., Santana Girao E., Valerio M., Munoz P., Fernandez Yunquera A., Statlender L., Yahav D., Franceschini E., Graziano E., Morelli M.C., Cescon M., Viale P., Lewis R., Bartoletti M., Pascale R., Campoli C., Coladonato S., Cristini F., Tumietto F., Siniscalchi A., Laici C., Ambretti S., Romagnoli R., De Rosa F.G., Muscatello A., Mangioni D., Gori A., Antonelli B., Dondossola D., Rossi G., Invernizzi F., Peghin M., Cillo U., Mussini C., Benedetto F.D., Terrabuio D.R.B., Bittante C.D., Toniolo A.D.R., Balbi E., Garcia J.H.P., Morras I., Ramos A., Cruz A.F., and Salcedo M.
- Subjects
Microbiology (medical) ,Adult ,medicine.medical_specialty ,medicine.medical_treatment ,Carbapenem-resistant enterobacteriaceae ,Liver transplantation ,CRE carriage ,CRE infection ,SOT ,liver transplantation ,Anti-Bacterial Agents ,Carbapenems ,Cohort Studies ,Humans ,Risk Factors ,Carbapenem-Resistant Enterobacteriaceae ,Enterobacteriaceae Infections ,Liver Transplantation ,03 medical and health sciences ,0302 clinical medicine ,Interquartile range ,Internal medicine ,Anti-Bacterial Agent ,Medicine ,030212 general & internal medicine ,Carbapenem ,Univariate analysis ,business.industry ,Risk Factor ,Area under the curve ,Nomogram ,Enterobacteriaceae Infection ,Transplantation ,Infectious Diseases ,030211 gastroenterology & hepatology ,Cohort Studie ,business ,Human ,Cohort study - Abstract
BackgroundPatients colonized with carbapenem-resistant Enterobacteriaceae (CRE) are at higher risk of developing CRE infection after liver transplantation (LT), with associated high morbidity and mortality. Prediction model for CRE infection after LT among carriers could be useful to target preventive strategies.MethodsMultinational multicenter cohort study of consecutive adult patients underwent LT and colonized with CRE before or after LT, from January 2010 to December 2017. Risk factors for CRE infection were analyzed by univariate analysis and by Fine-Gray subdistribution hazard model, with death as competing event. A nomogram to predict 30- and 60-day CRE infection risk was created.ResultsA total of 840 LT recipients found to be colonized with CRE before (n = 203) or after (n = 637) LT were enrolled. CRE infection was diagnosed in 250 (29.7%) patients within 19 (interquartile range [IQR], 9–42) days after LT. Pre- and post-LT colonization, multisite post-LT colonization, prolonged mechanical ventilation, acute renal injury, and surgical reintervention were retained in the prediction model. Median 30- and 60-day predicted risk was 15% (IQR, 11–24) and 21% (IQR, 15–33), respectively. Discrimination and prediction accuracy for CRE infection was acceptable on derivation (area under the curve [AUC], 74.6; Brier index, 16.3) and bootstrapped validation dataset (AUC, 73.9; Brier index, 16.6). Decision-curve analysis suggested net benefit of model-directed intervention over default strategies (treat all, treat none) when CRE infection probability exceeded 10%. The risk prediction model is freely available as mobile application at https://idbologna.shinyapps.io/CREPostOLTPredictionModel/.ConclusionsOur clinical prediction tool could enable better targeting interventions for CRE infection after transplant.
- Published
- 2021
10. L’évaluation psychologique des patients obèses demandeurs d’un anneau gastrique : quelle place pour le sujet ?
- Author
-
Dolhem-Campoli, C.
- Published
- 2007
- Full Text
- View/download PDF
11. Multiple Bilateral Pulmonary “Fungus Balls” in an Immunocompetent Patient Unsuitable for Surgical Treatment: Efficacy of Azoles Treatment
- Author
-
Capone, A., Di Bella, S., Chinello, P., Chiappetta, D., Campoli, C., and Petrosillo, N.
- Published
- 2013
- Full Text
- View/download PDF
12. Bloodstream infection caused by KPC-producing Klebsiella pneumoniae resistant to ceftazidime/avibactam: epidemiology and genomic characterization
- Author
-
Gaibani, P., primary, Re, M.C., additional, Campoli, C., additional, Viale, P.L., additional, and Ambretti, S., additional
- Published
- 2020
- Full Text
- View/download PDF
13. Helmintos parasitos de ovinos em pequenas propriedades nos municípios de Valentim Gentil, Meridiano e Votuporanga, região nordeste do Estado de São Paulo
- Author
-
Rigamonte, B, primary, Passos, V, additional, Romera, D, additional, Silva, R, additional, Campoli, C, additional, and Silva, G, additional
- Published
- 2019
- Full Text
- View/download PDF
14. A prospective multicentre study of the epidemiology and outcomes of bloodstream infection in cirrhotic patients
- Author
-
Bartoletti, M., primary, Giannella, M., additional, Lewis, R., additional, Caraceni, P., additional, Tedeschi, S., additional, Paul, M., additional, Schramm, C., additional, Bruns, T., additional, Merli, M., additional, Cobos-Trigueros, N., additional, Seminari, E., additional, Retamar, P., additional, Muñoz, P., additional, Tumbarello, M., additional, Burra, P., additional, Torrani Cerenzia, M., additional, Barsic, B., additional, Calbo, E., additional, Maraolo, A.E., additional, Petrosillo, N., additional, Galan-Ladero, M.A., additional, D'Offizi, G., additional, Bar Sinai, N., additional, Rodríguez-Baño, J., additional, Verucchi, G., additional, Bernardi, M., additional, Viale, P., additional, Campoli, C., additional, Siccardi, G., additional, Ambretti, S., additional, Stallmach, A., additional, Venditti, M., additional, Lucidi, C., additional, Ludovisi, S., additional, De Cueto, M., additional, Navarro, M.D., additional, Lopez Cortes, E., additional, Bouza, E., additional, Valerio, M., additional, Eworo, A., additional, Losito, R., additional, Senzolo, M., additional, Nadal, E., additional, Ottobrelli, A., additional, Varguvic, M., additional, Badia, C., additional, Borgia, G., additional, Gentile, I., additional, Buonomo, A.R., additional, Boumis, E., additional, Beteta-Lopez, A., additional, Rianda, A., additional, Taliani, G., additional, and Grieco, S., additional
- Published
- 2018
- Full Text
- View/download PDF
15. Antifungal prophylaxis in liver transplant recipients: one size does not fit all
- Author
-
Giannella, M., primary, Bartoletti, M., additional, Morelli, M., additional, Cristini, F., additional, Tedeschi, S., additional, Campoli, C., additional, Tumietto, F., additional, Bertuzzo, V., additional, Ercolani, G., additional, Faenza, S., additional, Pinna, A.D., additional, Lewis, R.E., additional, and Viale, P., additional
- Published
- 2016
- Full Text
- View/download PDF
16. Functional characterisation of HvCO1, the barley (Hordeum vulgare) flowering time ortholog of CONSTANS
- Author
-
Campoli, C., Drosse, B., Searle, I., Coupland, G., and von Korff, M.
- Published
- 2012
17. Why is Counting-by-Eye so Difficult? Effects of Spatial Structure and Reduced Luminance
- Author
-
Owens, D. A., primary, Benedict, J., additional, Campoli, C., additional, and Shah, M., additional
- Published
- 2014
- Full Text
- View/download PDF
18. INFLUÊNCIA DAS CONDIÇÕES SANITÁRIAS DOS EQUIPAMENTOS E DAS MÃOS DOS ORDENHADORES SOBRE A QUALIDADE MICROBIOLÓGICA DO LEITE / INFLUENCE OF SANITARY CONDITIONS OF THE EQUIPMENT AND MILKER HANDS ON THE MICROBIOLOGICAL QUALITY MILK
- Author
-
CAMPOLI, C. C., primary, GATTO, I. R. H, additional, and KOZUSNY-ANDREANI, D. I., additional
- Published
- 2013
- Full Text
- View/download PDF
19. Development and validation of a prediction model for severe respiratory failure in hospitalized patients with SARS-Cov-2 infection: a multicenter cohort study (PREDI-CO study)
- Author
-
Ciro Fulgaro, Ioannis Tzimas, Luigi Raumer, Marianna Meschiari, Marianna Menozzi, Gabriella Verucchi, Giada Rossini, Filippo Trapani, Giacomo Fornaro, Michela Semprini, Alessandra Cascavilla, Emanuele Campaci, Maddalena Giannella, Luigia Scudeller, Alessandro Zuccotti, Irid Baxhaku, Lucia Angelelli, Eleonora Zamparini, Annalisa Saracino, Alberto Zuppiroli, Cristina Basso, Elisabetta Pierucci, Agostino Rossi, Giulia Santangelo, Paolo Gaibani, Francesco Cristini, Francesca Volpato, Elisa Fronti, Giovanni Guaraldi, Alberto Sarti, Giorgio Legnani, Mattia Neri, Mauro Codeluppi, Adriana Badeanu, Giulio Virgili, Chiara Pironi, Lorenzo Marconi, Sara K. Tedeschi, Vidak Koprivika, Francesco Barchiesi, Luciano Attard, Matteo Rinaldi, Paola Laghetti, Stefano Antonini, Linda Bussini, Caterina Campoli, Giacomo Urbinati, Marco Merli, Nicholas Roncagli, Agnese Pratelli, Elena Rosselli Del Turco, Silvia Rapuano, Luca Guerra, Stefano Ianniruberto, Francesco Dell'Omo, Michele Bartoletti, Livia Pancaldi, Viola Guardigni, Fabio Tumietto, Giuseppe Sasdelli, Vito Marco Ranieri, Flovia Dauti, Giovanni Fasulo, Eugenia Francalanci, Nicola Dentale, Amalia Sanna Passino, Tommaso Zanaboni, Arianna Rubin, Davide Fiore Bavaro, Idina Zavatta, Massimo Puoti, Letizia Pasinelli, Maria Cristina Leoni, Pierluigi Viale, Oana Vatamanu, Elena Piccini, Renato Pascale, Cristina Mussini, Luca Esposito, Simona Coladonato, Alice Gori, Giulia Tesini, Lorenzo Badia, Mara D'Onofrio, Alberto Licci, Enrico Evangelisti, Guido Maria Liuzzi, Giacinto Pizzilli, Nicolò Rossi, Tommaso Tonetti, Marina Tadolini, Zeno Pasquini, Caterina Vocale, Bartoletti M., Giannella M., Scudeller L., Tedeschi S., Rinaldi M., Bussini L., Fornaro G., Pascale R., Pancaldi L., Pasquini Z., Trapani F., Badia L., Campoli C., Tadolini M., Attard L., Puoti M., Merli M., Mussini C., Menozzi M., Meschiari M., Codeluppi M., Barchiesi F., Cristini F., Saracino A., Licci A., Rapuano S., Tonetti T., Gaibani P., Ranieri V.M., Viale P., Raumer L., Guerra L., Tumietto F., Cascavilla A., Zamparini E., Verucchi G., Coladonato S., Rubin A., Ianniruberto S., Francalanci E., Volpato F., Virgili G., Rossi N., Del Turco E.R., Guardigni V., Fasulo G., Dentale N., Fulgaro C., Legnani G., Campaci E., Basso C., Zuppiroli A., Passino A.S., Tesini G., Angelelli L., Badeanu A., Rossi A., Santangelo G., Dauti F., Koprivika V., Roncagli N., Tzimas I., Liuzzi G.M., Baxhaku I., Pasinelli L., Neri M., Zanaboni T., Dell'Omo F., Vatamanu O., Gori A., Zavatta I., Antonini S., Pironi C., Piccini E., Esposito L., Zuccotti A., Urbinati G., Pratelli A., Sarti A., Semprini M., Evangelisti E., D'Onofrio M., Sasdelli G., Pizzilli G., Pierucci E., Rossini G., Vocale C., Marconi L., Leoni M.C., Fronti E., Guaraldi G., Bavaro D., Laghetti P., Bartoletti, M, Giannella, M, Scudeller, L, Tedeschi, S, Rinaldi, M, Bussini, L, Fornaro, G, Pascale, R, Pancaldi, L, Pasquini, Z, Trapani, F, Badia, L, Campoli, C, Tadolini, M, Attard, L, Puoti, M, Merli, M, Mussini, C, Menozzi, M, Meschiari, M, Codeluppi, M, Barchiesi, F, Cristini, F, Saracino, A, Licci, A, Rapuano, S, Tonetti, T, Gaibani, P, Ranieri, V, Viale, P, Raumer, L, Guerra, L, Tumietto, F, Cascavilla, A, Zamparini, E, Verucchi, G, Coladonato, S, Rubin, A, Ianniruberto, S, Francalanci, E, Volpato, F, Virgili, G, Rossi, N, Del Turco, E, Guardigni, V, Fasulo, G, Dentale, N, Fulgaro, C, Legnani, G, Campaci, E, Basso, C, Zuppiroli, A, Passino, A, Tesini, G, Angelelli, L, Badeanu, A, Rossi, A, Santangelo, G, Dauti, F, Koprivika, V, Roncagli, N, Tzimas, I, Liuzzi, G, Baxhaku, I, Pasinelli, L, Neri, M, Zanaboni, T, Dell'Omo, F, Vatamanu, O, Gori, A, Zavatta, I, Antonini, S, Pironi, C, Piccini, E, Esposito, L, Zuccotti, A, Urbinati, G, Pratelli, A, Sarti, A, Semprini, M, Evangelisti, E, D'Onofrio, M, Sasdelli, G, Pizzilli, G, Pierucci, E, Rossini, G, Vocale, C, Marconi, L, Leoni, M, Fronti, E, Guaraldi, G, Bavaro, D, and Laghetti, P
- Subjects
0301 basic medicine ,Male ,Logistic regression ,prognostic tool ,0302 clinical medicine ,Risk Factors ,Positive predicative value ,Severe acute respiratory syndrome coronavirus 2 ,030212 general & internal medicine ,Child ,Aged, 80 and over ,Framingham Risk Score ,Coronavirus disease 2019 ,Respiratory distress ,Lactate dehydrogenase ,General Medicine ,Middle Aged ,Prognosis ,Hospitalization ,Infectious Diseases ,Italy ,Child, Preschool ,Female ,Coronavirus Infections ,Respiratory Insufficiency ,Cohort study ,Microbiology (medical) ,Adult ,medicine.medical_specialty ,Respiratory rate ,Adolescent ,COVID-19 ,SARS-CoV-2 ,severe respiratory failure ,030106 microbiology ,Pneumonia, Viral ,Risk Assessment ,Sensitivity and Specificity ,Article ,03 medical and health sciences ,Betacoronavirus ,Young Adult ,Age ,Internal medicine ,medicine ,Humans ,Obesity ,Pandemics ,Aged ,Retrospective Studies ,business.industry ,Reproducibility of Results ,Retrospective cohort study ,Logistic Models ,Respiratory failure ,Multivariate Analysis ,business ,C-reactive proteine - Abstract
Objectives: We aimed to develop and validate a risk score to predict severe respiratory failure (SRF) among patients hospitalized with coronavirus disease-2019 (COVID-19). Methods: We performed a multicentre cohort study among hospitalized (>24 hours) patients diagnosed with COVID-19 from 22 February to 3 April 2020, at 11 Italian hospitals. Patients were divided into derivation and validation cohorts according to random sorting of hospitals. SRF was assessed from admission to hospital discharge and was defined as: SpO2 30 breaths/min or respiratory distress. Multivariable logistic regression models were built to identify predictors of SRF, β-coefficients were used to develop a risk score. Trial Registration NCT04316949. Results: We analysed 1113 patients (644 derivation, 469 validation cohort). Mean (±SD) age was 65.7 (±15) years, 704 (63.3%) were male. SRF occurred in 189/644 (29%) and 187/469 (40%) patients in the derivation and validation cohorts, respectively. At multivariate analysis, risk factors for SRF in the derivation cohort assessed at hospitalization were age ≥70 years (OR 2.74; 95% CI 1.66–4.50), obesity (OR 4.62; 95% CI 2.78–7.70), body temperature ≥38°C (OR 1.73; 95% CI 1.30–2.29), respiratory rate ≥22 breaths/min (OR 3.75; 95% CI 2.01–7.01), lymphocytes ≤900 cells/mm3 (OR 2.69; 95% CI 1.60–4.51), creatinine ≥1 mg/dL (OR 2.38; 95% CI 1.59–3.56), C-reactive protein ≥10 mg/dL (OR 5.91; 95% CI 4.88–7.17) and lactate dehydrogenase ≥350 IU/L (OR 2.39; 95% CI 1.11–5.11). Assigning points to each variable, an individual risk score (PREDI-CO score) was obtained. Area under the receiver-operator curve was 0.89 (0.86–0.92). At a score of >3, sensitivity, specificity, and positive and negative predictive values were 71.6% (65%–79%), 89.1% (86%–92%), 74% (67%–80%) and 89% (85%–91%), respectively. PREDI-CO score showed similar prognostic ability in the validation cohort: area under the receiver-operator curve 0.85 (0.81–0.88). At a score of >3, sensitivity, specificity, and positive and negative predictive values were 80% (73%–85%), 76% (70%–81%), 69% (60%–74%) and 85% (80%–89%), respectively. Conclusion: PREDI-CO score can be useful to allocate resources and prioritize treatments during the COVID-19 pandemic.
- Published
- 2020
20. Risk factors associated with bacteremia in COVID-19 patients admitted to intensive care unit: a retrospective multicenter cohort study
- Author
-
Cecilia Bonazzetti, Matteo Rinaldi, Andrea Giacomelli, Riccardo Colombo, Davide Ottolina, Sara Giordana Rimoldi, Cristina Pagani, Valentina Morena, Anna Lisa Ridolfo, Oana Vatamanu, Maria Eugenia Giacomini, Caterina Campoli, Letizia Oreni, Giuliano Rizzardini, Pierluigi Viale, Spinello Antinori, Maddalena Giannella, Bonazzetti C., Rinaldi M., Giacomelli A., Colombo R., Ottolina D., Rimoldi S.G., Pagani C., Morena V., Ridolfo A.L., Vatamanu O., Giacomini M.E., Campoli C., Oreni L., Rizzardini G., Viale P., Antinori S., and Giannella M.
- Subjects
Microbiology (medical) ,Charlson score ,Immunosuppressive therapy ,Infectious Diseases ,Bacteremia ,COVID-19 ,SOFA score ,Settore MED/17 - Malattie Infettive ,General Medicine - Abstract
Purpose This multicenter observational study was done to evaluate risk factors related to the development of BSI in patients admitted to ICU for COVID-19. Methods All patients with COVID-19 admitted in two COVID-19 dedicated ICUs in two different hospital between 02–2020 and 02–2021 were recruited. Result 537 patients were included of whom 265 (49.3%) experienced at least one BSI. Patients who developed bacteremia had a higher SOFA score [10 (8–12) vs 9 (7–10), p p p p p Conclusion A high SOFA score and a high Charlson score resulted associated with BSI’s development. Conversely, immunosuppressive therapy like steroids and tocilizumab, has no role in increasing the risk of bacteremia.
- Published
- 2022
21. A Proof of Concept of the Role of TDM-Based Clinical Pharmacological Advices in Optimizing Antimicrobial Therapy on Real-Time in Different Paediatric Settings
- Author
-
Milo Gatti, Pier Giorgio Cojutti, Caterina Campoli, Fabio Caramelli, Luigi Tommaso Corvaglia, Marcello Lanari, Andrea Pession, Stefania Ramirez, Pierluigi Viale, Federico Pea, Gatti M., Cojutti P.G., Campoli C., Caramelli F., Corvaglia L.T., Lanari M., Pession A., Ramirez S., Viale P., and Pea F.
- Subjects
medicine.medical_specialty ,clinical pharmacology advice ,Antimicrobial susceptibility ,RM1-950 ,neonatology ,law.invention ,Paediatric intensive care unit ,law ,Medicine ,Pharmacology (medical) ,Dosing ,Intensive care medicine ,Paediatric patients ,Original Research ,Voriconazole ,Pharmacology ,Clinical pharmacology ,medicine.diagnostic_test ,business.industry ,personalized antimicrobial therapy ,Antimicrobial ,paediatric intensive care unit ,paediatric onco-haematology ,Therapeutic drug monitoring ,Therapeutics. Pharmacology ,business ,paediatric emergency ,medicine.drug - Abstract
Introduction: Antimicrobial treatment is quite common among hospitalized children. The dynamic age-associated physiological variations coupled with the pathophysiological alterations caused by underlying illness and potential drug-drug interactions makes the implementation of appropriate antimicrobial dosing extremely challenging among paediatrics. Therapeutic drug monitoring (TDM) may represent a valuable tool for assisting clinicians in optimizing antimicrobial exposure. Clinical pharmacological advice (CPA) is an approach based on the correct interpretation of the TDM result by the MD Clinical Pharmacologist in relation to specific underlying conditions, namely the antimicrobial susceptibility of the clinical isolate, the site of infection, the pathophysiological characteristics of the patient and/or the drug-drug interactions of cotreatments. The aim of this study was to assess the role of TDM-based CPAs in providing useful recommendations for the real-time personalization of antimicrobial dosing regimens in various paediatric settings.Materials and methods: Paediatric patients who were admitted to different settings of the IRCCS Azienda Ospedaliero-Universitaria of Bologna, Italy (paediatric intensive care unit [ICU], paediatric onco-haematology, neonatology, and emergency paediatric ward), between January 2021 and June 2021 and who received TDM-based CPAs on real-time for personalization of antimicrobial therapy were retrospectively assessed. Demographic and clinical features, CPAs delivered in relation to different settings and antimicrobials, and type of dosing adjustments were extracted. Two indicators of performance were identified. The number of dosing adjustments provided over the total number of delivered CPAs. The turnaround time (TAT) of CPAs according to a predefined scale (optimal, 48 h).Results: Overall, 247 CPAs were delivered to 53 paediatric patients (mean 4.7 ± 3.7 CPAs/patient). Most were delivered to onco-haematological patients (39.6%) and to ICU patients (35.8%), and concerned mainly isavuconazole (19.0%) and voriconazole (17.8%). Overall, CPAs suggested dosing adjustments in 37.7% of cases (24.3% increases and 13.4% decreases). Median TAT was 7.5 h (IQR 6.1–8.8 h). Overall, CPAs TAT was optimal in 91.5% of cases, and suboptimal in only 0.8% of cases.Discussion: Our study provides a proof of concept of the helpful role that TDM-based real-time CPAs may have in optimizing antimicrobial exposure in different challenging paediatric scenarios.
- Published
- 2021
22. Breakthrough invasive fungal infection after liver transplantation in patients on targeted antifungal prophylaxis: a prospective multicentre study
- Author
-
Maddalena Giannella, Milo Gatti, Russell E. Lewis, Maria Cristina Morelli, Caterina Campoli, Michele Bartoletti, Fabrizio Di Benedetto, Simona Coladonato, Matteo Rinaldi, Monica Cricca, Pierluigi Viale, Patrizia Burra, Simone Ambretti, Alberto Ferrarese, Renato Pascale, Cristina Mussini, Francesco Cristini, Sara K. Tedeschi, Erica Franceschini, Matteo Cescon, Umberto Cillo, Antonio Siniscalchi, Rinaldi M., Bartoletti M., Ferrarese A., Franceschini E., Campoli C., Coladonato S., Pascale R., Tedeschi S., Gatti M., Cricca M., Ambretti S., Siniscalchi A., Morelli M.C., Cescon M., Cillo U., Di Benedetto F., Burra P., Mussini C., Cristini F., Lewis R., Viale P., and Giannella M.
- Subjects
Antifungal ,Adult ,medicine.medical_specialty ,Antifungal Agents ,Orthotopic liver transplantation ,medicine.drug_class ,medicine.medical_treatment ,antifungal prophylaxis ,breakthrough IFI ,infection risk ,invasive fungal infection ,liver transplantation ,030230 surgery ,Liver transplantation ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,medicine ,antifungal prophylaxi ,Antifungal Agent ,Humans ,In patient ,Renal replacement therapy ,Prospective Studies ,Prospective cohort study ,Transplantation ,Adult patients ,business.industry ,Original Articles ,Prospective Studie ,Infectious Diseases ,surgical procedures, operative ,Mycoses ,030211 gastroenterology & hepatology ,Original Article ,business ,Echinocandins ,Invasive Fungal Infections ,Human - Abstract
Objective: To investigate the rate of and the risk factors for breakthrough-IFI (b-IFI) after orthotopic liver transplantation (OLT) according to the new definition proposed by Mycoses-Study-Group-Education-and-Research-Consortium (MSG-ERC) and the European-Confederation-of-Medical-Mycology (ECMM). Methods: Multicenter prospective study of adult patients who underwent OLT at three Italian hospitals, from January 2015 to December 2018. Targeted antifungal prophylaxis (TAP) protocol was developed and shared among participating centers. Follow-up was 1-year after OLT. B-IFI was defined as infection occurring during exposure to antifungal prophylaxis. Risk factors for b-IFI were analyzed among patients exposed to prophylaxis by univariable analysis. Results: We enrolled 485 OLT patients. Overall compliance to TAP protocol was 64.3%, 220 patients received antifungal prophylaxis, 172 according to TAP protocol. Twenty-nine patients were diagnosed of IFI within 1year after OLT. Of them, 11 presented with b-IFI within 17 (IQR 11-33) and 16 (IQR 4-30) days from OLT and from antifungal onset, respectively. Then out of 11 patients with b-IFI were classified as having high risk of IFI and were receiving anti-mould prophylaxis, nine with echinocandins and one with polyenes. Comparison of patients with and without b-IFI showed significant differences for prior Candida colonization, need of renal replacement therapy after OLT, re-operation, and CMV infection (whole blood CMV-DNA >100000 copies/mL). Although non-significant, a higher rate of b-IFI in patients on echinocandins was observed (8.2% vs 1.8%, P=.06). Conclusions: We observed 5% of b-IFI among OLT patients exposed to antifungal prophylaxis. The impact of echinocandins on b-IFI risk in this setting should be further explored.
- Published
- 2021
23. Risk factors for candidaemia in hospitalized patients with liver cirrhosis: a multicentre case–control–control study
- Author
-
Michele Bartoletti, S. Incicco, Paolo Caraceni, Matteo Rinaldi, P. Viale, Maddalena Giannella, Simone Ambretti, M.C. Morelli, Salvatore Piano, Luigia Scudeller, Caterina Campoli, Paolo Angeli, Daniele Roberto Giacobbe, Matteo Bassetti, Maurizio Baldassarre, F. Del Puente, Alberto Enrico Maraolo, Linda Bussini, Monica Cricca, Z. Pasquini, Ivan Gentile, Bartoletti, M., Rinaldi, M., Pasquini, Z., Scudeller, L., Piano, S., Giacobbe, D. R., Maraolo, A. E., Bussini, L., Del Puente, F., Incicco, S., Angeli, P., Giannella, M., Baldassarre, M., Caraceni, P., Campoli, C., Morelli, M. C., Cricca, M., Ambretti, S., Gentile, I., Bassetti, M., Viale, P., Bartoletti, Michele, Rinaldi, Matteo, Pasquini, Zeno, Scudeller, Luigia, Piano, Salvatore, Giacobbe, Daniele Roberto, Maraolo, Alberto Enrico, Bussini, Linda, Del Puente, Filippo, Incicco, Simone, Angeli, Paolo, Giannella, Maddalena, Baldassarre, Maurizio, Caraceni, Paolo, Campoli, Caterina, Morelli, Maria Cristina, Cricca, Monica, Ambretti, Simone, Gentile, Ivan, Bassetti, Matteo, and Viale, Pierluigi
- Subjects
0301 basic medicine ,Liver Cirrhosis ,Male ,Multivariate analysis ,Cirrhosis ,Hospitalized patients ,medicine.medical_treatment ,Severity of Illness Index ,Liver cirrhosi ,Tertiary Care Centers ,chemistry.chemical_compound ,0302 clinical medicine ,Model for End-Stage Liver Disease ,fluids and secretions ,Risk Factors ,hemic and lymphatic diseases ,Medicine ,030212 general & internal medicine ,Candida ,General Medicine ,Middle Aged ,Acute-on-chronic liver failure ,Infectious Diseases ,Blood ,Italy ,Female ,Central venous catheter ,Microbiology (medical) ,medicine.medical_specialty ,030106 microbiology ,Protective factor ,Bloodstream infection ,Rifaximin ,03 medical and health sciences ,Candidaemia ,Internal medicine ,Humans ,Candidemia ,Liver cirrhosis ,bloodstream infection ,Aged ,Retrospective Studies ,business.industry ,biochemical phenomena, metabolism, and nutrition ,medicine.disease ,equipment and supplies ,bacterial infections and mycoses ,Survival Analysis ,Parenteral nutrition ,chemistry ,Case-Control Studies ,business - Abstract
Objectives: The aim of this study was to evaluate the risk factors for candidaemia in patients with liver cirrhosis. Methods: This was a case–control–control (1:2:2) study performed in four Italian tertiary centres from 2006 to 2015. Cases were patients with liver cirrhosis developing candidaemia. For every case of candidaemia we enrolled two additional patients undergoing blood cultures for suspected infection yielding isolation of a bacterial pathogen (control A) and two additional patients undergoing blood cultures for suspected infection yielding negative results (control B). Patients were matched according to age, sex and model for end stage liver disease at hospital admission. Results: During the study period 90 cases, 180 controls A and 180 controls B were included. At multivariate analysis assessed by means of multinomial conditional regression models, factors independently associated with candidaemia were previous (15 days (RRR 4.63 (95% CI 2.11–10.18), p
- Published
- 2021
24. Serum bactericidal titres for monitoring antimicrobial therapy: current status and potential role in the management of multidrug-resistant Gram-negative infections
- Author
-
Maddalena Giannella, Irene Zaghi, Caterina Campoli, Paolo Gaibani, Simone Ambretti, Michele Bartoletti, Russell E. Lewis, Pierluigi Viale, Zaghi I., Gaibani P., Campoli C., Bartoletti M., Giannella M., Ambretti S., Viale P., and Lewis R.E.
- Subjects
0301 basic medicine ,Microbiology (medical) ,medicine.medical_specialty ,medicine.drug_class ,030106 microbiology ,Antibiotics ,Pharmacokinetic ,Microbial Sensitivity Tests ,Antibiotic monitoring ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,Meta-analysis ,Pharmacodynamics ,Pharmacokinetics ,Serum bactericidal titre ,Gram-Negative Bacteria ,Medicine ,Humans ,Serum Bactericidal Test ,Meta-analysi ,030212 general & internal medicine ,Pharmacodynamic ,medicine.diagnostic_test ,business.industry ,General Medicine ,Antimicrobial ,Prognosis ,Anti-Bacterial Agents ,Multiple drug resistance ,Critical appraisal ,Infectious Diseases ,Therapeutic drug monitoring ,Diagnostic odds ratio ,business ,Gram-Negative Bacterial Infections - Abstract
Background Serum bactericidal titres (SBTs) were widely used in the 1970s and 1980s to monitor antimicrobial therapy but are now seldom recommended. It is the only laboratory test that integrates drug pharmacodynamics, host pharmacokinetics and synergistic or antagonistic interactions of antimicrobial combinations into a single index of antimicrobial activity. We hypothesized that SBTs could play a renewed role in monitoring antibiotic treatment of multidrug-resistant Gram-negative infections. However, the last critical appraisal of the test was published over 30 years ago. Objectives This narrative review provides an updated assessment of the SBT test and its methodological limitations. We performed a diagnostic meta-analysis to estimate the value of SBTs for predicting clinical failure or death during antibiotic treatment. Sources A comprehensive literature search of PubMed including all English publications was performed in December 2019 using the Medical Subject Headings (MeSH search terms “serum”, “bactericidal”, “inhibitory”, “titre”, “monitoring”, “anti-infective agents” “antimicrobial therapy” and “therapeutic drug monitoring”). Content Although standardized methods for performing SBTs were approved in 1999, the test remains labour intensive, and results may not be available until 72 hr. However, the use of non-culture-based endpoints (i.e. spectrophotometric or fluorescent) may shorten test time to 24 hr. Despite considerable heterogeneity in published studies, a meta-analysis of 11 evaluable studies published from 1974 to 2007 indicated a critical SBT result (peak SBT ≤1:8 or trough ≤1:2) is associated with a diagnostic odds ratio for clinical failure during antibiotic treatment of 12.27 (95% confidence interval 5.28–28.54) and a 5.32 (95% 1.32–21.42) odds of death. Implications SBTs have prognostic value for identifying patients at high risk for antibiotic treatment failure, but the slow turnaround time of the current test limits its clinical utility. Standardization of a more rapid SBT testing method is needed.
- Published
- 2020
25. Comparative serum bactericidal activity of meropenem-based combination regimens against extended-spectrum beta-lactamase and KPC-producing Klebsiella pneumoniae
- Author
-
Sara K. Tedeschi, Michele Bartoletti, Donatella Lombardo, Pierluigi Viale, Matteo Conti, Maddalena Giannella, Maria Paola Landini, Maria Carla Re, Caterina Campoli, Russell E. Lewis, Rita Mancini, Paolo Gaibani, Simone Ambretti, Gaibani P., Lombardo D., Bartoletti M., Ambretti S., Campoli C., Giannella M., Tedeschi S., Conti M., Mancini R., Landini M.P., Re M.C., Viale P., and Lewis R.E.
- Subjects
0301 basic medicine ,Male ,Serum ,Klebsiella pneumoniae ,medicine.medical_treatment ,Tigecycline ,Gastroenterology ,0302 clinical medicine ,Medical microbiology ,Tandem Mass Spectrometry ,polycyclic compounds ,030212 general & internal medicine ,biology ,Microbial Sensitivity Test ,General Medicine ,Middle Aged ,Anti-Bacterial Agents ,Infectious Diseases ,Critical Illne ,Drug Therapy, Combination ,Female ,medicine.drug ,Human ,Microbiology (medical) ,medicine.medical_specialty ,Critical Illness ,030106 microbiology ,Microbial Sensitivity Tests ,Meropenem ,beta-Lactamases ,Serum bactericidal assay ,03 medical and health sciences ,Cmin ,Internal medicine ,Anti-Bacterial Agent ,medicine ,Humans ,Aged ,Microbial Viability ,business.industry ,Colistin ,biochemical phenomena, metabolism, and nutrition ,bacterial infections and mycoses ,biology.organism_classification ,Klebsiella Infections ,KPC ,Pharmacodynamics ,ESßL ,Beta-lactamase ,bacteria ,business ,Klebsiella Infection ,Chromatography, Liquid - Abstract
Combination therapies are frequently used in the treatment of multidrug-resistant Klebsiella pneumoniae infection without consensus regarding which combination is the most effective. We compared bactericidal titres from sera collected from critically ill patients receiving meropenem plus tigecycline (n= 5), meropenem plus colistin (n= 5), or meropenem, colistin and tigecycline (n= 5) against K. pneumoniae isolates that included ESBL-producing (n= 7) and KPC-producing strains (n= 14) with varying sensitivity patterns to colistin and tigecycline. Meropenem concentrations (Cmin) were measured in all samples by LC-MS/MS, and indexed to respective pathogen MICs to explore differences in patterns of bactericidal activity for two versus three drug combination regimens. All combination regimens achieved higher SBTs against ESBL (median reciprocal titre 128, IQR 32–256) versus KPC (4, IQR 2–32) strains. Sera from patients treated with meropenem-colistin yielded higher median SBTs (256, IQR 64–512) than either meropenem-tigecycline (32, IQR 8–256; P' 0.001). The addition of tigecycline was associated with a lower probability of achieving a reciprocal SBT above 8 when meropenem concentrations were below the MIC (P= 0.04). Although the clinical significance is unknown, sera from patients receiving tigecycline-based combination regimens produce lower serum bactericidal titres against ESBL or KPC-producing K. pneumoniae. SBTs may represent a useful complimentary endpoint for comparing pharmacodynamics of combinations regimens for MDR Enterobacteriaceae.
- Published
- 2019
26. The impact of carbapenemase-producing Enterobacteriaceae colonization on infection risk after liver transplantation: a prospective observational cohort study
- Author
-
Matteo Cescon, Fabio Tumietto, Simona Coladonato, Francesco Cristini, Pierluigi Viale, Maddalena Giannella, Russell E. Lewis, Michele Bartoletti, Matteo Rinaldi, Caterina Campoli, Antonio Daniele Pinna, Sara K. Tedeschi, Simone Ambretti, Antonio Siniscalchi, M.C. Morelli, Renato Pascale, Valentina Rosa Bertuzzo, Giannella M., Bartoletti M., Campoli C., Rinaldi M., Coladonato S., Pascale R., Tedeschi S., Ambretti S., Cristini F., Tumietto F., Siniscalchi A., Bertuzzo V., Morelli M.C., Cescon M., Pinna A.D., Lewis R., and Viale P.
- Subjects
Colonization ,Infection risk ,0301 basic medicine ,Microbiology (medical) ,Adult ,Male ,medicine.medical_specialty ,medicine.medical_treatment ,030106 microbiology ,Liver transplantation ,Carbapenem-resistant ,03 medical and health sciences ,Liver disease ,0302 clinical medicine ,Interquartile range ,Risk Factors ,Internal medicine ,medicine ,Humans ,030212 general & internal medicine ,Prospective Studies ,Carbapenemase-producing Enterobacteriaceae ,Prospective cohort study ,business.industry ,Incidence (epidemiology) ,Incidence ,Hazard ratio ,Enterobacteriaceae Infections ,General Medicine ,Middle Aged ,medicine.disease ,Liver Transplantation ,Infectious Diseases ,Carbapenem-Resistant Enterobacteriaceae ,Female ,business ,Asymptomatic carrier ,Cohort study ,Follow-Up Studies - Abstract
Objective To investigate the impact of colonization with carbapenemase-producing Enterobacteriaceae (CPE) on the CPE infection risk after liver transplantation (LT). Methods Prospective cohort study of all adult patients undergoing LT at our centre over an 8-year period (2010–2017). Individuals were screened for CPE colonization by rectal swabs at inclusion onto the waiting list, immediately before LT and weekly after LT until hospital discharge. Asymptomatic carriers did not receive decolonization, anti-CPE prophylaxis or pre-emptive antibiotic therapy. Participants were followed up for 1 year after LT. Results We analysed 553 individuals who underwent a first LT, 38 were colonized with CPE at LT and 104 acquired colonization after LT. CPE colonization rates at LT and acquired after LT increased significantly over the study period: incidence rate ratios (IRR) 1.21 (95% CI 1.05–1.39) and 1.17 (95% CI 1.07–1.27), respectively. Overall, 57 patients developed CPE infection within a median of 31 (interquartile range 11–115) days after LT, with an incidence of 3.05 cases per 10 000 LT-recipient-days and a non-significant increase over the study period (IRR 1.11, 95% CI 0.98–1.26). In multivariable analysis, CPE colonization at LT (hazard ratio (HR) 18.50, 95% CI 6.76–50.54) and CPE colonization acquired after LT (HR 16.89, 95% CI 6.95–41.00) were the strongest risk factors for CPE infection, along with combined transplant (HR 2.60, 95% CI 1.20–5.59), higher Model for End-Stage Liver Disease at the time of LT (HR 1.03, 95% CI 1.00–1.07), prolonged mechanical ventilation (HR 2.63, 95% CI 1.48–4.67), re-intervention (HR 2.16, 95% CI 1.21–3.84) and rejection (HR 2.81, 95% CI 1.52–5.21). Conclusions CPE colonization at LT or acquired after LT were the strongest predictors of CPE infection. Prevention strategies focused on LT candidates and recipients colonized with CPE should be investigated.
- Published
- 2019
27. Antifungal prophylaxis in liver transplant recipients: one size does not fit all
- Author
-
Michele Bartoletti, Pierluigi Viale, Sara K. Tedeschi, Russell E. Lewis, Fabio Tumietto, Francesco Cristini, M.C. Morelli, Antonio Daniele Pinna, Maddalena Giannella, Caterina Campoli, Stefano Faenza, Giorgio Ercolani, Valentina Rosa Bertuzzo, Giannella, M, Bartoletti, M., Morelli, M., Cristini, F., Tedeschi, S., Campoli, C., Tumietto, F., Bertuzzo, V., Ercolani, G., Faenza, S., Pinna, A.D., Lewis, R.E., and Viale, P.
- Subjects
Male ,medicine.medical_specialty ,Antifungal Agents ,medicine.medical_treatment ,Infectious Disease ,030230 surgery ,Liver transplantation ,invasive fungal infection ,Aspergillosis ,Risk Assessment ,Medication Adherence ,03 medical and health sciences ,Liver disease ,0302 clinical medicine ,Risk Factors ,Internal medicine ,medicine ,antifungal prophylaxi ,Humans ,Renal replacement therapy ,Fluconazole ,Candida ,Retrospective Studies ,Transplantation ,Proportional hazards model ,business.industry ,Incidence ,Retrospective cohort study ,Antibiotic Prophylaxis ,Middle Aged ,medicine.disease ,Transplant Recipients ,Liver Transplantation ,Surgery ,Aspergillus ,Infectious Diseases ,Etiology ,Female ,030211 gastroenterology & hepatology ,business ,Invasive Fungal Infections ,medicine.drug - Abstract
Background Targeted antifungal prophylaxis against Candida species or against Candida species and Aspergillus species, according to individual patient risk factors (RFs), is recommended by experts. However, recent studies have reported fluconazole is as effective as broader spectrum antifungals for preventing invasive fungal infection (IFI) after liver transplantation (LT). Methods We performed a retrospective cohort study of all adult patients who underwent LT at our 1420-bed tertiary teaching hospital, from June 2010 to December 2014, to assess the rate and etiology of IFI within 100 days after LT, to investigate the compliance with targeted prophylaxis, and to analyze risk factors for developing IFI. Results In total, 303 patients underwent LT. Patients were classified as having low (no RFs), intermediate (1 RF for invasive candidiasis [IC]), and high risk (1 RF for invasive aspergillosis [IA] or ≥2 RFs for IC) for IFI in 20%, 30%, and 50% of cases, respectively. A total of 139 patients received antifungal prophylaxis: 98 with a mold-active drug and 41 with fluconazole. Overall adherence to targeted prophylaxis was 53%. Nineteen patients (6.3%) developed IFI: 7 IC and 12 IA. Multivariate Cox regression analysis, adjusted for median model for end-stage liver disease score at LT, stratification risk group, and adherence to targeted prophylaxis, showed that graft dysfunction, renal replacement therapy, and prophylaxis with fluconazole were independent risk factors for IFI. Seven of the 9 patients who received fluconazole prophylaxis and developed IFI were classified as having high risk for IFI, and 6 developed IA. Conclusion Recommended stratification is accurate for predicting patients at very high risk for IFI, who should receive prophylaxis with a mold-active drug.
- Published
- 2016
- Full Text
- View/download PDF
28. Bloodstream infection caused by KPC-producing Klebsiella pneumoniae resistant to ceftazidime/avibactam: epidemiology and genomic characterization
- Author
-
Simone Ambretti, Paolo Gaibani, Maria Carla Re, Pierluigi Viale, Caterina Campoli, Gaibani P., Re M.C., Campoli C., Viale P.L., and Ambretti S.
- Subjects
Microbiology (medical) ,Klebsiella pneumoniae ,Avibactam ,Population ,Ceftazidime ,Bacteremia ,Microbial Sensitivity Tests ,bla ,Meropenem/vaborbactam resistance ,Meropenem ,Microbiology ,Tertiary Care Centers ,chemistry.chemical_compound ,Ceftazidime/avibactam resistance ,Drug Resistance, Multiple, Bacterial ,copy number ,polycyclic compounds ,medicine ,Humans ,education ,Vaborbactam ,education.field_of_study ,Porin deficiency ,Whole Genome Sequencing ,biology ,Incidence ,Genomics ,General Medicine ,biochemical phenomena, metabolism, and nutrition ,bacterial infections and mycoses ,biology.organism_classification ,Antimicrobial ,Ceftazidime/avibactam ,Anti-Bacterial Agents ,Klebsiella Infections ,Drug Combinations ,KPC ,Carbapenem-Resistant Enterobacteriaceae ,Infectious Diseases ,Italy ,chemistry ,Mutation ,D179Y mutation ,Azabicyclo Compounds ,Genome, Bacterial ,medicine.drug - Abstract
Objectives The aim of this study was to evaluate the incidence of ceftazidime/avibactam resistance among Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae (KPC-Kp) strains isolated from patients with bloodstream infection. Methods We collected 120 carbapenemase producing Enterobacteriaceae (CPE) strains from unique patients hospitalized in two Italian hospitals between January 2018 to February 2019. Strains were phenotypically characterized for the type of carbapenemase production and susceptibility to ceftazidime/avibactam. Ceftazidime/avibactam-resistant strains were characterized by whole-genome sequencing. Results During the study period, we characterized 105 (87.5%) KPC producers among a total of 120 CPE strains. Ceftazidime/avibactam resistance was found in three KPC-Kp strains isolated from patients with no history of previous ceftazidime/avibactam-based treatment. Of note, two out of three ceftazidime–avibactam-resistant KPC-Kp were also resistant to meropenem/vaborbactam. Genomic characterization showed that a ceftazidime/avibactam-resistant KPC-Kp harboured a mixed population with D179Y mutated KPC-2, while the other two ceftazidime–avibactam-resistant KPC-Kp possessed non-functional ompK35-ompK37 and mutated ompK36 porins associated with higher copy number of blaKPC gene. Conclusions Our results showed that incidence of ceftazidime/avibactam resistance emerged in KCP-Kp strains independently from previous antimicrobial exposure. Resistance to ceftazidime/avibactam was associated with mutations within the blaKPC gene or porin deficiency associated with higher blaKPC copy number and is also related to the meropenem/vaborbactam resistance.
- Published
- 2020
- Full Text
- View/download PDF
29. Management of immunosuppressive therapy in liver transplant recipients who develop bloodstream infection
- Author
-
Pierluigi Viale, Francesca Furii, Simone Ambretti, Michele Bartoletti, Caterina Campoli, Antonio Daniele Pinna, Maria Cristina Morelli, Matteo Cescon, Renato Pascale, Francesco Cristini, Sara K. Tedeschi, Maddalena Giannella, Valentina Rosa Bertuzzo, Giacomo Vandi, and Bartoletti M, Vandi G, Furii F, Bertuzzo V, Ambretti S, Tedeschi S, Pascale R, Cristini F, Campoli C, Morelli MC, Cescon M, Pinna AD, Viale P, Giannella M
- Subjects
Graft Rejection ,Male ,medicine.medical_specialty ,medicine.medical_treatment ,030230 surgery ,liver transplant, immunosuppression, bloodstream infection ,03 medical and health sciences ,0302 clinical medicine ,Risk Factors ,Internal medicine ,Sepsis ,medicine ,Humans ,Retrospective Studies ,Immunosuppression Therapy ,Transplantation ,business.industry ,Proportional hazards model ,Septic shock ,Mortality rate ,Immunosuppression ,Retrospective cohort study ,Antibiotic Prophylaxis ,Middle Aged ,medicine.disease ,Discontinuation ,Anti-Bacterial Agents ,Liver Transplantation ,Survival Rate ,Infectious Diseases ,Immunosuppressive drug ,Treatment Outcome ,Propensity score matching ,030211 gastroenterology & hepatology ,Female ,business ,Immunosuppressive Agents - Abstract
Background Data about the optimal management of immunosuppressive therapy in liver transplant (LT) recipients with bloodstream infection (BSI) are missing. We aimed to describe the management of immunosuppressive therapy at diagnosis of BSI in LT recipients and to assess its impact on 28-day mortality. Methods We performed a single-center retrospective study of all LT recipients diagnosed with BSI, over 10-year period. Multivariate Cox regression analysis of risk factors for all cause 28-day mortality was adjusted for the propensity score of being managed with "any reduction" in immunosuppressive therapy at the diagnosis of BSI. Results We identified 209 episodes of BSI in 157 LT recipients: 107 (68%) male, median age 54 (IQR 48-63) years. "Any reduction" was made in 90 (43%) cases including: dosage reduction of ≥1 immunosuppressive drug in 31 (15%), discontinuation of ≥1 immunosuppressive drug in 28 (13%), both dosage reduction and discontinuation in 13 (6%), complete withdrawal of immunosuppressive therapy in 18 (9%) cases. All-cause 28-day mortality rate was 13.4%, varying from 22% to 7% (P = .002) in cases with and without "any reduction". Cox regression showed septic shock (aHR 3.15, P = .007) and "any reduction" (aHR 2.50, P = .02) as independent risk factors for all-cause 28-day mortality, while Escherichia coli (aHR 0.38, P = .03) and source control (aHR 0.43, P = .04) were protective factors. The final model did not change after the introduction of the propensity score for "any reduction". Conclusions Any reduction in the immunosuppressive therapy was common and was associated with worse outcome in LT recipients developing BSI.
- Published
- 2018
30. A prospective multicentre study of the epidemiology and outcomes of bloodstream infection in cirrhotic patients
- Author
-
Ivan Gentile, Jesús Rodríguez-Baño, Alia Eworo, Gloria Taliani, E. Nadal, M. Valerio, A. Beteta-Lopez, Christoph Schramm, Pierluigi Viale, Bruno Baršić, Cristina Badia, S. Ludovisi, Alberto Enrico Maraolo, Gabriella Verucchi, Elena Seminari, M. de Cueto, Maddalena Giannella, E. Boumis, S. Grieco, Pilar Retamar, Nazaret Cobos-Trigueros, Caterina Campoli, Emilio Bouza, Mauro Bernardi, Patrizia Burra, M. Varguvic, Sara K. Tedeschi, Esther Calbo, María Dolores González-Ripoll Navarro, N. Bar Sinai, Mario Venditti, Andreas Stallmach, Russell E. Lewis, Guglielmo Borgia, Patricia Muñoz, Antonio Riccardo Buonomo, Mical Paul, Gianpiero D'Offizi, Michele Bartoletti, Paolo Caraceni, M.A. Galan-Ladero, Mario Tumbarello, Manuela Merli, Marco Senzolo, G. Siccardi, R. Losito, A. Ottobrelli, E. Lopez Cortes, A. Rianda, Cristina Lucidi, Simone Ambretti, Nicola Petrosillo, M. Torrani Cerenzia, Tony Bruns, Bartoletti, M., Giannella, M., Lewis, R., Caraceni, P., Tedeschi, S., Paul, M., Schramm, C., Bruns, T., Merli, M, Cobos-Trigueros, N., Seminari, E., Retamar, P., Muñoz, P., Tumbarello, M., Burra, P., Torrani Cerenzia, M., Barsic, B., Calbo, E., Maraolo, A.E., Petrosillo, N., Galan-Ladero, M.A., D'Offizi, G., Bar Sinai, N., Rodríguez-Baño, J., Verucchi, G., Bernardi, M., Viale, P., Bartoletti, M, Giannella, M, Lewis, R, Caraceni, P, Tedeschi, S, Paul, M, Schramm, C, Bruns, T, Cobos-trigueros, N, Seminari, E, Retamar, P, Muñoz, P, Tumbarello, M, Burra, P, Torrani Cerenzia, M, Barsic, B, Calbo, E, Maraolo, Ae, Petrosillo, N, Galan-ladero, Ma, D'Offizi, G, Bar Sinai, N, Rodríguez-baño, J, Verucchi, G, Bernardi, M, Viale, P, Campoli, C, Siccardi, G, Ambretti, S, Stallmach, A, Venditti, M, Lucidi, C, Ludovisi, S, De Cueto, M, Navarro, Md, Lopez Cortes, E, Bouza, E, Valerio, M, Eworo, A, Losito, R, Senzolo, M, Nadal, E, Ottobrelli, A, Varguvic, M, Badia, C, Borgia, G, Gentile, I, Buonomo, Ar, Boumis, E, Beteta-lopez, A, Rianda, A, Taliani, G, and Grieco, S.
- Subjects
Liver Cirrhosis ,Male ,Microbiology (medical) ,medicine.medical_specialty ,Multidrug-resistant pathogen ,Comorbidity ,Bloodstream infection ,Bacterial infections ,Bloodstream infections ,CLIF-SOFA ,Multidrug-resistant pathogens ,Logistic regression ,Liver cirrhosi ,03 medical and health sciences ,0302 clinical medicine ,Risk Factors ,Sepsis ,Internal medicine ,Epidemiology ,medicine ,Humans ,Prospective Studies ,030212 general & internal medicine ,Mortality ,Risk factor ,Intensive care medicine ,Prospective cohort study ,Aged ,Proportional hazards model ,business.industry ,Liver cirrhosis ,Infectious Diseases ,Mortality rate ,Hazard ratio ,Disease Management ,Drug Resistance, Microbial ,General Medicine ,Middle Aged ,Prognosis ,Patient Outcome Assessment ,Population Surveillance ,Female ,030211 gastroenterology & hepatology ,Bacterial infection ,business ,Cohort study - Abstract
ESGBIS/BICHROME Study Group: C. Campoli, G. Siccardi, S. Ambretti, A. Stallmach, M. Venditti, C. Lucidi, S. Ludovisi, M. De Cueto, M. D. Navarro, E. Lopez Cortes, E. Bouza, M. Valerio, A. Eworo, R. Losito, M. Senzolo, E. Nadal, A. Ottobrelli, M. Varguvic, C. Badia, G. Borgia, I. Gentile, A. R. Buonomo, E. Boumis, A. Beteta-Lopez, A. Rianda, G. Taliani, S. Grieco., [Objectives] To describe the current epidemiology of bloodstream infection (BSI) in patients with cirrhosis; and to analyse predictors of 30-day mortality and risk factors for antibiotic resistance., [Methods] Cirrhotic patients developing a BSI episode were prospectively included at 19 centres in five countries from September 2014 to December 2015. The discrimination of mortality risk scores for 30-day mortality were compared by area under the receiver operator risk and Cox regression models. Risk factors for multidrug-resistant organisms (MDRO) were assessed with a logistic regression model., [Results] We enrolled 312 patients. Gram-negative bacteria, Gram-positive bacteria and Candida spp. were the cause of BSI episodes in 53%, 47% and 7% of cases, respectively. The 30-day mortality rate was 25% and was best predicted by the Sequential Organ Failure Assessment (SOFA) and Chronic Liver Failure–SOFA (CLIF-SOFA) score. In a Cox regression model, delayed (>24 hours) antibiotic treatment (hazard ratio (HR) 7.58; 95% confidence interval (CI) 3.29–18.67; p < 0.001), inadequate empirical therapy (HR 3.14; 95% CI 1.93–5.12; p < 0.001) and CLIF-SOFA score (HR 1.35; 95% CI 1.28–1.43; p < 0.001) were independently associated with 30-day mortality. Independent risk factors for MDRO (31% of BSIs) were previous antimicrobial exposure (odds ratio (OR) 2.91; 95% CI 1.73–4.88; p < 0.001) and previous invasive procedures (OR 2.51; 95% CI 1.48–4.24; p 0.001), whereas spontaneous bacterial peritonitis as BSI source was associated with a lower odds of MDRO (OR 0.30; 95% CI 0.12–0.73; p 0.008)., [Conclusions] MDRO account for nearly one-third of BSI in cirrhotic patients, often resulting in delayed or inadequate empirical antimicrobial therapy and increased mortality rates. Our data suggest that improved prevention and treatment strategies for MDRO are urgently needed in the liver cirrhosis patients.
- Published
- 2018
- Full Text
- View/download PDF
31. Multiple bilateral pulmonary 'fungus balls' in an immunocompetent patient unsuitable for surgical treatment: efficacy of azoles treatment
- Author
-
Nicola Petrosillo, S. Di Bella, C. Campoli, Alessandro Capone, D. Chiappetta, Pierangelo Chinello, Capone, A, Di Bella, S, Chinello, P, Chiappetta, D, Campoli, C, and Petrosillo, N
- Subjects
Male ,Surgical resection ,Antifungal ,medicine.medical_specialty ,Antifungal Agents ,medicine.drug_class ,Veterinary (miscellaneous) ,Fungus ball ,Aspergillosis ,Applied Microbiology and Biotechnology ,Microbiology ,medicine ,Humans ,aspergillosi ,aspergillosis ,Mycetoma ,Surgical treatment ,Lung ,Aged ,Voriconazole ,business.industry ,High mortality ,aspergilloma ,Triazoles ,medicine.disease ,Surgery ,Radiography ,Pyrimidines ,Treatment Outcome ,Pulmonary Aspergillosis ,business ,Agronomy and Crop Science ,Aspergilloma ,medicine.drug - Abstract
Data guiding management of pulmonary mycetomas are based on uncontrolled trials and case reports. Surgical resection represents a definitive treatment associated with high mortality and sometimes not feasible due to clinical conditions. We report a case of an immunocompetent patient with multiple pulmonary mycetomas, suggestive for probable chronic aspergillosis, in which surgery was contraindicated. The patient experienced a good response to long-term oral voriconazole therapy with remarkable clinical and radiological improvement at three-month follow-up. In cases of probable chronic aspergillomas, when surgery is contraindicated, long-term antifungal therapy with voriconazole seems to be a valid alternative option.
- Published
- 2013
32. Clostridium difficile infection in the elderly
- Author
-
Stefano, Di Bella, Alessandro, Capone, Maria, Musso, Maddalena, Giannella, Agapito, Tarasi, Emma, Johnson, Fabrizio, Taglietti, Caterina, Campoli, Nicola, Petrosillo, Di Bella, S, Capone, A, Musso, M, Giannella, M, Tarasi, A, Johnson, E, Taglietti, F, Campoli, C, Petrosillo, N, Di Bella, Stefano, Capone, Alessandro, Musso, Maria, Giannella, Maddalena, Tarasi, Agapito, Johnson, Emma, Taglietti, Fabrizio, Campoli, Caterina, and Petrosillo, Nicola
- Subjects
Clostridium difficile ,elderly ,advanced age ,geriatric patient ,Clostridioides difficile ,Clostridium Infections ,Humans ,Clostridium Infection ,Aged ,Human - Abstract
The incidence of C. difficile infections (CDI) in the elderly continues to rise and infection is associated with increased morbidity and mortality when compared to those affected in younger age-groups. Immunosenescence may be a contributory factor yet the exact immune responses that may protect against CDI are incompletely understood. Increased exposure to antibiotics, frequent and/or prolonged hospital admissions and residing in long-term care facilities provide multiple opportunities for host and pathogen to coincide. This review explores the epidemiology, diagnostic parameters and management of the spectrum of disease in the geriatric population. Deaths attributed to CDI are most common in the elderly population and are a major contributor to gastroenteritis-associated mortality in many countries. The elderly represent an at-risk population from this pathogen and efforts must be directed to preventing infection and optimising treatment in this group.
- Published
- 2013
33. Impact of Inflammatory Burden on Voriconazole Exposure in Oncohematological Pediatric Patients Receiving Antifungal Prophylaxis after Allogeneic HCT.
- Author
-
Gatti M, Campoli C, Muratore E, Belotti T, Masetti R, Lanari M, Viale P, and Pea F
- Abstract
(1) Background: The impact of inflammation on voriconazole exposure in oncohematological pediatric patients represents a debated issue. We aimed to investigate the impact of serum C-reactive protein (CRP), procalcitonin (PCT), and interleukin-6 (IL-6) levels on voriconazole exposure in oncohematological pediatric patients requiring allogeneic hematopoietic stem cell transplantation (HCT). (2) Methods: Pediatric patients undergoing allogeneic HCT and receiving therapeutic drug monitoring (TDM)-guided voriconazole as primary antifungal prophylaxis between January 2021 and December 2023 were included. The ratio between concentration and dose (C/D) of voriconazole was used as a surrogate marker of total clearance. A receiving operating characteristic curve analysis was performed by using CRP, PCT, or IL-6 values as the test variable and voriconazole C/D ratio > 0.188 or >0.375 (corresponding to a trough concentration value [C
min ] of 3 mg/L normalized to the maintenance dose of 16 mg/kg/day in patients of age < 12 years and of 8 mg/kg/day in those ≥12 years, respectively) as the state variable. Area under the curve (AUC) and 95% confidence interval (CI) were calculated. (3) Results: Overall, 39 patients were included. The median (IQR) voriconazole Cmin was 1.7 (0.7-3.0) mg/L. A CRP value > 8.49 mg/dL (AUC = 0.72; 95%CI 0.68-0.76; p < 0.0001), a PCT value > 2.6 ng/mL (AUC = 0.71; 95%CI 0.63-0.77; p < 0.0001), and an IL-6 value > 27.9 pg/mL (AUC = 0.80; 95%CI 0.71-0.88; p < 0.0001) were significantly associated with voriconazole overexposure. Consistent results were found in patients aged <12 and ≥12 years. (4) Conclusions: A single specific threshold of inflammatory biomarkers may be linked to a significantly higher risk of voriconazole exposure in oncohematological pediatric patients after HCT, irrespective of age. Adopting a TDM-guided strategy could be useful for minimizing the risk of voriconazole overexposure.- Published
- 2024
- Full Text
- View/download PDF
34. Mollaret's Meningitis due to Herpes Simplex Virus 2: A Case Report and Review of the Literature.
- Author
-
Gabrielli L, Banchini I, Petrisli E, Piccirilli G, Venturoli S, Pavoni M, Cantiani A, Lanna F, Campoli C, Montironi M, Giannella M, and Lazzarotto T
- Abstract
Mollaret's meningitis is a rare neurological disorder characterized by recurrent episodes of aseptic lymphocytic meningitis, often associated with herpes simplex virus 2 (HSV-2) infection. We report the case of a 39 y.o. Italian woman who experienced four episodes of aseptic lymphocytic meningitis between 2004 and 2023, diagnosed as Mollaret's meningitis. In each episode, the patient presented with fever, severe headache and photophobia. In two episodes cutaneous vesicles in the left gluteal area preceding meningitis symptoms were also reported. A diagnostic evaluation included a physical-chemical analysis and a real-time PCR of the cerebrospinal fluid (CSF). The CSF presented pleocytosis with lymphocytic predominance and a positive HSV-2 load, with a peak of 1234 copies/mL. The patient was treated successfully with acyclovir, and the symptoms resolved without neurological sequelae. This case highlights the importance of comprehensive diagnostic testing and vigilant monitoring to manage Mollaret's syndrome effectively.
- Published
- 2024
- Full Text
- View/download PDF
35. A GDSL-motif Esterase/Lipase Affects Wax and Cutin Deposition and Controls Hull-Caryopsis Attachment in Barley.
- Author
-
Campoli C, Eskan M, McAllister T, Liu L, Shoesmith J, Prescott A, Ramsay L, Waugh R, and McKim SM
- Subjects
- Mutation, Plant Epidermis metabolism, Plant Epidermis genetics, Amino Acid Motifs, Plant Leaves genetics, Plant Leaves metabolism, Phenotype, Hordeum genetics, Hordeum enzymology, Hordeum metabolism, Waxes metabolism, Plant Proteins metabolism, Plant Proteins genetics, Membrane Lipids metabolism, Esterases metabolism, Esterases genetics, Gene Expression Regulation, Plant
- Abstract
The cuticle covering aerial organs of land plants is well known to protect against desiccation. Cuticles also play diverse and specialized functions, including organ separation, depending on plant and tissue. Barley shows a distinctive cuticular wax bloom enriched in β-diketones on leaf sheaths, stem nodes and internodes and inflorescences. Barley also develops a sticky surface on the outer pericarp layer of its grain fruit leading to strongly adhered hulls, 'covered grain', important for embryo protection and seed dispersal. While the transcription factor-encoding gene HvNUDUM (HvNUD) appears essential for adherent hulls, little is understood about how the pericarp cuticle changes during adhesion or whether changes in pericarp cuticles contribute to another phenotype where hulls partially shed, called 'skinning'. To that end, we screened barley lines for hull adhesion defects, focussing on the Eceriferum (= waxless, cer) mutants. Here, we show that the cer-xd allele causes defective wax blooms and compromised hull adhesion, and results from a mutation removing the last 10 amino acids of the GDS(L) [Gly, Asp, Ser, (Leu)]-motif esterase/lipase HvGDSL1. We used severe and moderate HvGDSL1 alleles to show that complete HvGDSL1 function is essential for leaf blade cuticular integrity, wax bloom deposition over inflorescences and leaf sheaths and pericarp cuticular ridge formation. Expression data suggest that HvGDSL1 may regulate hull adhesion independently of HvNUD. We found high conservation of HvGDSL1 among barley germplasm, so variation in HvGDSL1 unlikely leads to grain skinning in cultivated barley. Taken together, we reveal a single locus which controls adaptive cuticular properties across different organs in barley., (© The Author(s) 2024. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists.)
- Published
- 2024
- Full Text
- View/download PDF
36. A 10-Year Retrospective Study on Pediatric Visceral Leishmaniasis in a European Endemic Area: Diagnostic and Short-Course Therapeutic Strategies.
- Author
-
Dondi A, Manieri E, Gambuti G, Varani S, Campoli C, Zama D, Pierantoni L, Baldazzi M, Prete A, Attard L, Lanari M, and Melchionda F
- Abstract
Background: Visceral leishmaniasis (VL) is a potentially fatal disease, with an increasing occurrence in northern Italy, affecting children and both immunocompetent and immunocompromised adults., Methods: This retrospective study conducted at the St. Orsola University Hospital of Bologna, Italy, evaluates the characteristics of 16 children (with a median age of 14.3 months) who were hospitalized between 2013 and 2022 for VL., Results: Seventy-five percent of patients presented with a triad of fever, cytopenia, and splenomegaly. An abdominal ultrasound examination revealed splenomegaly and hypoechoic spleen abnormalities in 93.8% and 73.3% of cases, respectively. Five VL cases were complicated by secondary hemophagocytic lymphohistiocytosis. Eleven patients were treated with a single 10 mg/kg dose of Liposomal Amphotericin B (L-AmB), while five received two doses (total of 20 mg/kg); one of the former groups experienced a recurrence. The fever generally decreased 48 h after the first L-AmB dose, and hemoglobin levels normalized within a month. The splenomegaly resolved in approximately 4.5 months., Conclusions: Pediatricians should consider VL in children with fever of an unknown origin, anemia, cytopenia, and splenomegaly. In our experience, abdominal ultrasounds and molecular tests on peripheral blood contributed to diagnosis without the need for bone marrow aspiration. The short-course therapy with two 10 mg/kg doses of L-AmB is safe and effective.
- Published
- 2023
- Full Text
- View/download PDF
37. Relationship Between Real-time TDM-guided Pharmacodynamic Target Attainment of Continuous Infusion Beta-lactam Monotherapy and Microbiologic Outcome in the Treatment of Critically Ill Children With Severe Documented Gram-negative Infections.
- Author
-
Gatti M, Campoli C, Latrofa ME, Ramirez S, Sasso T, Mancini R, Caramelli F, Viale P, and Pea F
- Abstract
Objectives: To explore the relationship between real-time therapeutic drug monitoring (TDM)-guided pharmacodynamic target attainment of continuous infusion (CI) beta-lactam monotherapy and microbiological outcome in the treatment of critically ill children with severe documented Gram-negative infections., Methods: Observational, monocentric, retrospective study of critically ill patients receiving CI piperacillin-tazobactam, ceftazidime, or meropenem in monotherapy for documented Gram-negative infections optimized by means of a real-time TDM-guided strategy. Average steady-state beta-lactam concentrations (C ss ) were calculated for each patient, and the beta-lactam C ss /minimum inhibitory concentration (MIC) ratio was selected as a pharmacodynamic parameter of efficacy. The C ss /MIC ratio was defined as optimal if ≥4, quasi-optimal if between 1 and 4, and suboptimal if <1. The relationship between C ss /MIC and microbiological outcome was assessed., Results: Forty-six TDM assessments were carried out in 21 patients [median age 2 (interquartile range: 1-8) years]. C ss /MIC ratios were optimal in 76.2% of cases. Patients with optimal C ss /MIC ratios had both a significantly higher microbiological eradication rate (75.0% vs. 0.0%; P = 0.006) and lower resistance development rate (25.0% vs. 80.0%; P = 0.047) than those with quasi-optimal or suboptimal C ss /MIC ratios. Quasi-optimal/suboptimal C ss /MIC ratio occurred more frequently when patients had infections caused by pathogens with MIC values above the European Committee on Antimicrobial Susceptibility Testing clinical breakpoint (100.0% vs. 6.3%; P < 0.001)., Conclusions: Real-time TDM-guided pharmacodynamic target attainment of CI beta-lactam monotherapy allowed to maximize treatment efficacy in most critically ill children with severe Gram-negative infections. Attaining early optimal C ss /MIC ratios of CI beta-lactams could be a key determinant associated with microbiologic eradication during the treatment of Gram-negative infections. Larger prospective studies are warranted for confirming our findings., Competing Interests: M.G. has received personal fees from Angelini and Shionogi, outside the submitted work. PV has served as a consultant for bioMérieux, Gilead, Merck Sharp & Dohme, Nabriva, Nordic Pharma, Pfizer, Thermo Fisher, and Venatorx, and received payment for serving on the speaker’s bureaus for Correvio, Gilead, Merck Sharp & Dohme, Nordic Pharma, and Pfizer, outside the submitted work. F.P. reports personal fees from Angelini, Basilea Pharmaceutica, Gilead, Hikma, MSD, Pfizer, Sanofi-Aventis, Shionogi, Thermo Fisher, and Accelerate Diagnostics, outside the submitted work; has participated in speaker’s bureau for Accelerate Diagnostics, Angelini, Basilea Pharmaceutica, Gilead, Hikma, MSD, Pfizer, Sanofi-Aventis, Shionogi, Thermo Fisher, and as consultant for Angelini, Basilea Pharmaceutica, Gilead, MSD, Pfizer, Shionogi, outside the submitted work. The other authors have no conflicts of interest to disclose., (Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc.)
- Published
- 2023
- Full Text
- View/download PDF
38. Comparison between available early antiviral treatments in outpatients with SARS-CoV-2 infection: a real-life study.
- Author
-
Rinaldi M, Campoli C, Gallo M, Marzolla D, Zuppiroli A, Riccardi R, Casarini M, Riccucci D, Malosso M, Bonazzetti C, Pascale R, Tazza B, Pasquini Z, Marconi L, Curti S, Giannella M, and Viale P
- Subjects
- Humans, Male, Aged, COVID-19 Drug Treatment, SARS-CoV-2, Antiviral Agents therapeutic use, Ritonavir therapeutic use, Outpatients, COVID-19
- Abstract
Purpose: To investigate the clinical impact of three available antivirals for early COVID-19 treatment in a large real-life cohort., Methods: Between January and October 2022 all outpatients tested positive for SARS-CoV-2 referring to IRCCS S. Orsola hospital treated with an early antiviral therapy were enrolled. A comparison between patients treated with nirmatrelvir/ritonavir (NTV/r), molnupiravir (MPV) and remdesivir (RDV) was conducted in term of indications and outcome. To account for differences between treatment groups a propensity score analysis was performed. After estimating the weights, we fitted a survey-weighted Cox regression model with inverse-probability weighting with hospital admission/death versus clinical recovery as the primary outcome., Results: Overall 1342 patients were enrolled, 775 (57.8%), 360 (26.8%) and 207 (15.4%) in MPV, NTV/r and RDV group, respectively. Median age was 73 (59-82) years, male sex was 53.4%. Primary indication was immunosuppression (438, 32.6%), the median time from symptom onset to drug administration was 3 [2-4] days. Overall, clinical recovery was reached in 96.9% of patients, with hospital admission rate of 2.6%. No significant differences were found in clinical recovery nor hospitalization. Cox regression showed a decreased probability of hospital admission/ death among prior vaccinated patients compared with unvaccinated (HR 0.31 [95%CI 0.14-0.70], p = 0.005]). No difference in hospitalization rates in early treatment compared to late treatment were found., Conclusions: No differences among MPV, NTV/r and RDV in terms of clinical recovery or hospitalization were found. Patients not vaccinated had a significant increased risk of hospitalization., (© 2023. BioMed Central Ltd., part of Springer Nature.)
- Published
- 2023
- Full Text
- View/download PDF
39. Isolation and characterization of the gene HvFAR1 encoding acyl-CoA reductase from the cer-za.227 mutant of barley (Hordeum vulgare) and analysis of the cuticular barrier functions.
- Author
-
Müller Y, Patwari P, Stöcker T, Zeisler-Diehl V, Steiner U, Campoli C, Grewe L, Kuczkowska M, Dierig MM, Jose S, Hetherington AM, Acosta IF, Schoof H, Schreiber L, and Dörmann P
- Subjects
- Plant Leaves metabolism, Water metabolism, Saccharomyces cerevisiae metabolism, Waxes metabolism, Mutation genetics, Plant Epidermis metabolism, Nuclear Proteins metabolism, Cyclin-Dependent Kinase Inhibitor Proteins genetics, Cyclin-Dependent Kinase Inhibitor Proteins metabolism, Hordeum genetics, Hordeum metabolism, Arabidopsis genetics, Arabidopsis metabolism, Arabidopsis Proteins metabolism, Saccharomyces cerevisiae Proteins metabolism
- Abstract
The cuticle is a protective layer covering aerial plant organs. We studied the function of waxes for the establishment of the cuticular barrier in barley (Hordeum vulgare). The barley eceriferum mutants cer-za.227 and cer-ye.267 display reduced wax loads, but the genes affected, and the consequences of the wax changes for the barrier function remained unknown. Cuticular waxes and permeabilities were measured in cer-za.227 and cer-ye.267. The mutant loci were isolated by bulked segregant RNA sequencing. New cer-za alleles were generated by genome editing. The CER-ZA protein was characterized after expression in yeast and Arabidopsis cer4-3. Cer-za.227 carries a mutation in HORVU5Hr1G089230 encoding acyl-CoA reductase (FAR1). The cer-ye.267 mutation is located to HORVU4Hr1G063420 encoding β-ketoacyl-CoA synthase (KAS1) and is allelic to cer-zh.54. The amounts of intracuticular waxes were strongly decreased in cer-ye.267. The cuticular water loss and permeability of cer-za.227 were similar to wild-type (WT), but were increased in cer-ye.267. Removal of epicuticular waxes revealed that intracuticular, but not epicuticular waxes are required to regulate cuticular transpiration. The differential decrease in intracuticular waxes between cer-za.227 and cer-ye.267, and the removal of epicuticular waxes indicate that the cuticular barrier function mostly depends on the presence of intracuticular waxes., (© 2023 The Authors. New Phytologist © 2023 New Phytologist Foundation.)
- Published
- 2023
- Full Text
- View/download PDF
40. Corrigendum to: "Development and validation of a prediction model for severe respiratory failure in hospitalized patients with SARS-CoV-2 infection: a multicentre cohort study (PREDI-CO study)" Clinical Microbiology and Infection 26 (2020) 1545-1553.
- Author
-
Bartoletti M, Giannella M, Scudeller L, Tedeschi S, Rinaldi M, Bussini L, Fornaro G, Pascale R, Pancaldi L, Pasquini Z, Trapani F, Badia L, Campoli C, Tadolini M, Attard L, Puoti M, Merli M, Mussini C, Menozzi M, Meschiari M, Codeluppi M, Barchiesi F, Cristini F, Saracino A, Licci A, Rapuano S, Tonetti T, Gaibani P, Ranieri VM, and Viale P
- Published
- 2023
- Full Text
- View/download PDF
41. Outcome of early treatment of SARS-CoV-2 infection in patients with haematological disorders.
- Author
-
Mikulska M, Testi D, Russo C, Balletto E, Sepulcri C, Bussini L, Dentone C, Magne F, Policarpo S, Campoli C, Miselli F, Cilli A, Ghiggi C, Aquino S, Di Grazia C, Giannella M, Giacobbe DR, Vena A, Raiola AM, Bonifazi F, Zinzani P, Cavo M, Lemoli R, Angelucci E, Viale P, Bassetti M, and Bartoletti M
- Subjects
- Humans, Retrospective Studies, SARS-CoV-2, Antibodies, Monoclonal, Antiviral Agents therapeutic use, COVID-19, Hematologic Diseases, Hematologic Neoplasms complications, Hematologic Neoplasms therapy
- Abstract
Outcome of early treatment of COVID-19 with antivirals or anti-spike monoclonal antibodies (MABs) in patients with haematological malignancies (HM) is unknown. A retrospective study of HM patients treated for mild/moderate COVID-19 between March 2021 and July 2022 was performed. The main composite end-point was treatment failure (severe COVID-19 or COVID-19-related death). We included 328 consecutive patients who received MABs (n = 120, 37%; sotrovimab, n = 73) or antivirals (n = 208, 63%; nirmatrelvir/ritonavir, n = 116) over a median of two days after symptoms started; 111 (33.8%) had non-Hodgkin lymphoma (NHL); 89 (27%) were transplant/CAR-T (chimaeric antigen receptor T-cell therapy) recipients. Most infections (n = 309, 94%) occurred during the Omicron period. Failure developed in 31 patients (9.5%). Its independent predictors were older age, fewer vaccine doses, and treatment with MABs. Rate of failure was lower in the Omicron versus the pre-Omicron period (7.8% versus 36.8%, p < 0.001). During the Omicron period, predictors of failure were age, fewer vaccine doses and diagnosis of acute myeloid leukaemia/myelodysplastic syndrome (AML/MDS). Independent predictors of longer viral shedding were age, comorbidities, hospital admission at diagnosis, NHL/CLL, treatment with MABs. COVID-19-associated mortality was 3.4% (n = 11). The mortality in those who developed severe COVID-19 after early treatment was 26% in the Omicron period. Patients with HM had a significant risk of failure of early treatment, even during the Omicron period, with high mortality rate., (© 2023 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.)
- Published
- 2023
- Full Text
- View/download PDF
42. Risk factors associated with bacteremia in COVID-19 patients admitted to intensive care unit: a retrospective multicenter cohort study.
- Author
-
Bonazzetti C, Rinaldi M, Giacomelli A, Colombo R, Ottolina D, Rimoldi SG, Pagani C, Morena V, Ridolfo AL, Vatamanu O, Giacomini ME, Campoli C, Oreni L, Rizzardini G, Viale P, Antinori S, and Giannella M
- Subjects
- Humans, Cohort Studies, Intensive Care Units, Risk Factors, Retrospective Studies, COVID-19 complications, COVID-19 epidemiology, Bacteremia epidemiology
- Abstract
Purpose: This multicenter observational study was done to evaluate risk factors related to the development of BSI in patients admitted to ICU for COVID-19., Methods: All patients with COVID-19 admitted in two COVID-19 dedicated ICUs in two different hospital between 02-2020 and 02-2021 were recruited., Result: 537 patients were included of whom 265 (49.3%) experienced at least one BSI. Patients who developed bacteremia had a higher SOFA score [10 (8-12) vs 9 (7-10), p < 0.001], had been intubated more frequently [95.8% vs 75%, p < 0.001] and for a median longer time [16 days (9-25) vs 8 days (5-14), p < 0.001]. Patients with BSI had a median longer ICU stay [18 days (12-31.5) vs 9 days (5-15), p < 0.001] and higher mortality [54% vs 42.3%, p < 0.001] than those who did not develop it. Development of BSI resulted in a higher SOFA score [aHR 1.08 (95% CI 1.03-1.12)] and a higher Charlson score [csAHR 1.15 (95% CI 1.05-1.25)]., Conclusion: A high SOFA score and a high Charlson score resulted associated with BSI's development. Conversely, immunosuppressive therapy like steroids and tocilizumab, has no role in increasing the risk of bacteremia., (© 2022. The Author(s).)
- Published
- 2023
- Full Text
- View/download PDF
43. Conserved signalling components coordinate epidermal patterning and cuticle deposition in barley.
- Author
-
Liu L, Jose SB, Campoli C, Bayer MM, Sánchez-Diaz MA, McAllister T, Zhou Y, Eskan M, Milne L, Schreiber M, Batstone T, Bull ID, Ramsay L, von Wettstein-Knowles P, Waugh R, Hetherington AM, and McKim SM
- Subjects
- Carbon Dioxide metabolism, Gene Expression Regulation, Plant, MAP Kinase Kinase Kinases metabolism, Plant Epidermis metabolism, Waxes metabolism, Hordeum genetics, Hordeum metabolism
- Abstract
Faced with terrestrial threats, land plants seal their aerial surfaces with a lipid-rich cuticle. To breathe, plants interrupt their cuticles with adjustable epidermal pores, called stomata, that regulate gas exchange, and develop other specialised epidermal cells such as defensive hairs. Mechanisms coordinating epidermal features remain poorly understood. Addressing this, we studied two loci whose allelic variation causes both cuticular wax-deficiency and misarranged stomata in barley, identifying the underlying genes, Cer-g/ HvYDA1, encoding a YODA-like (YDA) MAPKKK, and Cer-s/ HvBRX-Solo, encoding a single BREVIS-RADIX (BRX) domain protein. Both genes control cuticular integrity, the spacing and identity of epidermal cells, and barley's distinctive epicuticular wax blooms, as well as stomatal patterning in elevated CO
2 conditions. Genetic analyses revealed epistatic and modifying relationships between HvYDA1 and HvBRX-Solo, intimating that their products participate in interacting pathway(s) linking epidermal patterning with cuticular properties in barley. This may represent a mechanism for coordinating multiple adaptive features of the land plant epidermis in a cultivated cereal., (© 2022. The Author(s).)- Published
- 2022
- Full Text
- View/download PDF
44. Predictive model for bacterial co-infection in patients hospitalized for COVID-19: a multicenter observational cohort study.
- Author
-
Giannella M, Rinaldi M, Tesini G, Gallo M, Cipriani V, Vatamanu O, Campoli C, Toschi A, Ferraro G, Horna CS, Bartoletti M, Ambretti S, Violante F, Viale P, and Curti S
- Subjects
- Adult, Aged, Anti-Bacterial Agents therapeutic use, COVID-19 Testing, Cohort Studies, Female, Hospitalization, Humans, Male, Retrospective Studies, Bacterial Infections diagnosis, Bacterial Infections epidemiology, COVID-19 diagnosis, COVID-19 epidemiology, Coinfection diagnosis, Coinfection epidemiology
- Abstract
Objective: The aim of our study was to build a predictive model able to stratify the risk of bacterial co-infection at hospitalization in patients with COVID-19., Methods: Multicenter observational study of adult patients hospitalized from February to December 2020 with confirmed COVID-19 diagnosis. Endpoint was microbiologically documented bacterial co-infection diagnosed within 72 h from hospitalization. The cohort was randomly split into derivation and validation cohort. To investigate risk factors for co-infection univariable and multivariable logistic regression analyses were performed. Predictive risk score was obtained assigning a point value corresponding to β-coefficients to the variables in the multivariable model. ROC analysis in the validation cohort was used to estimate prediction accuracy., Results: Overall, 1733 patients were analyzed: 61.4% males, median age 69 years (IQR 57-80), median Charlson 3 (IQR 2-6). Co-infection was diagnosed in 110 (6.3%) patients. Empirical antibiotics were started in 64.2 and 59.5% of patients with and without co-infection (p = 0.35). At multivariable analysis in the derivation cohort: WBC ≥ 7.7/mm
3 , PCT ≥ 0.2 ng/mL, and Charlson index ≥ 5 were risk factors for bacterial co-infection. A point was assigned to each variable obtaining a predictive score ranging from 0 to 5. In the validation cohort, ROC analysis showed AUC of 0.83 (95%CI 0.75-0.90). The optimal cut-point was ≥2 with sensitivity 70.0%, specificity 75.9%, positive predictive value 16.0% and negative predictive value 97.5%. According to individual risk score, patients were classified at low (point 0), intermediate (point 1), and high risk (point ≥ 2). CURB-65 ≥ 2 was further proposed to identify patients at intermediate risk who would benefit from early antibiotic coverage., Conclusions: Our score may be useful in stratifying bacterial co-infection risk in COVID-19 hospitalized patients, optimizing diagnostic testing and antibiotic use., (© 2022. The Author(s).)- Published
- 2022
- Full Text
- View/download PDF
45. Real-World Comparison of Isavuconazole and Voriconazole in Terms of the Need for Dosage Adjustments Guided by Clinical Pharmacological Advice During Primary Prophylaxis of Invasive Fungal Infections in Pediatric Patients with Hemato-Oncological Malignancies.
- Author
-
Gatti M, Campoli C, Belotti T, Cojutti PG, Masetti R, Pession A, Viale P, and Pea F
- Subjects
- Antifungal Agents, Azoles therapeutic use, Child, Humans, Nitriles, Pyridines, Retrospective Studies, Triazoles, Voriconazole therapeutic use, Invasive Fungal Infections drug therapy, Invasive Fungal Infections prevention & control, Neoplasms drug therapy
- Abstract
Background: Limited evidence concerning optimal azole dosing regimens currently exists for antifungal prophylaxis in hemato-oncological pediatric patients., Methods: Hemato-oncological children receiving intravenous or oral isavuconazole or voriconazole for primary antifungal prophylaxis at IRCCS Azienda Ospedaliero-Universitaria of Bologna during November 2020 to October 2021 and undergoing CPA programs based on real-time therapeutic drug monitoring (TDM) were retrospectively analyzed. CPAs for isavuconazole and voriconazole and the number of dosage adjustments were collected. Normalized trough concentrations [(C min )/dose/kg] were calculated for both drugs at each TDM assessment, and the coefficient of variation was determined. The efficacy and safety of the drugs were evaluated., Results: Sixteen hemato-oncological pediatric patients received azole prophylaxis (mean age and weight: 9.1 ± 4.9 years and 32.6 ± 16.0 kg; 6 isavuconazole and 10 voriconazole). Sixty and 89 CPAs were delivered as isavuconazole and voriconazole, respectively. Dosage adjustments were needed in 3.3% of cases for isavuconazole and 53.9% of cases for voriconazole ( P < 0.001). At first TDM, achievement of the desired target during standard dosing regimens was higher for isavuconazole (83.3%) than for voriconazole (10.0%; P = 0.008). Dispersion of normalized concentrations was higher for voriconazole (CV = 139.1% vs. CV = 79.4%). Elevation of ALT and aspartate aminotransferase levels between baseline and the third month was higher in patients receiving voriconazole (median, 28 vs. 90 U/L; P = 0.038, and 19 vs. 65.5 U/L; P = 0.002)., Conclusions: Our findings suggest that there is limited variability in isavuconazole exposure in hemato-oncological pediatric patients receiving azole prophylaxis , resulting in a low need for CPA-guided dosage adjustments., Competing Interests: M. Gatti reports grants from Angelini S.p.A. outside the submitted work. F. Pea reports personal fees from Angelini, Basilea Pharmaceutica, Gilead, Hikma, MSD, Pfizer, Sanofi–Aventis, Shionogi, Thermo Fisher, and Accelerate Diagnostics outside the submitted work, has participated in speaker's bureaus for Accelerate Diagnostics, Angelini, Basilea Pharmaceutica, Gilead, Hikma, MSD, Pfizer, Sanofi-Aventis, Shionogi, Thermo Fisher, and has served as consultants for Angelini, Basilea Pharmaceutica, Gilead, MSD, Pfizer, and Shionogi outside the submitted work. P. Viale has served as a consultant for bioMérieux, Gilead, Merck Sharp & Dohme, Nabriva, Nordic Pharma, Pfizer, Thermo Fisher, and Venatorx and received payment for serving on speaker's bureaus for Correvio, Gilead, Merck Sharp & Dohme, Nordic Pharma, and Pfizer outside the submitted work. The other authors declare no potential conflicts of interest related to this study., (Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.)
- Published
- 2022
- Full Text
- View/download PDF
46. Neutralizing monoclonal antibodies for early treatment of hospital-acquired SARS-CoV-2 infection in hematologic patients.
- Author
-
Bussini L, Testi D, Tazza B, Oltolini C, Mastaglio S, Sepulcri C, Campoli C, Trapani F, Pasquini Z, Zappulo E, Bassetti M, Viale P, Mikulska M, and Bartoletti M
- Abstract
Efficacy of early treatment with anti-SARS-CoV-2 spike protein monoclonal antibodies (mAbs) for nosocomial SARS-CoV-2 infection in hematologic patients is unknown. Retrospective, cohort study conducted in four Italian teaching hospitals. We included adult patients with hematologic malignancies and hospital-acquired SARS-CoV-2 infection diagnosed between November 2020 and December 2021. The principal exposure variable was administration of mAbs. The primary endpoint was clinical failure dea composite outcome of mortality and/or invasive and noninvasive ventilation within 90 days from infection onset. We included 52 patients with hospital-acquired SARS-CoV-2 infection. Males were 29 (60%), median age was 62 (interquartile range [IQR] 48-70). Forty-five (86%) patients were on chemotherapy or had received chemotherapy within 30 days. MAbs were administered in 19/52 (36%) patients. Clinical failure occurred in 22 (42%) patients; 21% (4/19) in mAbs group versus 54% (18/33) in non-mAbs group ( p = 0.03). Other predictors of clinical failure were older age (median [IQR] 69 [61-72] versus 58 [46-66], p = 0.001), and higher Charlson comorbidity index (median [IQR], 5 [3.25-5] versus 3 [2-5], p = 0.002). At multivariable Cox regression model, mAbs were independently associated with a significantly lower rate of clinical failure (HR 0.11, 95% CI 0.01-0.85, p = 0.01), after adjusting for confounders. In conclusion, mAbs are promising for early treatment of hematologic patients with healthcare-related SARS-CoV-2 infection., Competing Interests: The authors declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of the research reported., (© 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd.)
- Published
- 2022
- Full Text
- View/download PDF
47. Antimicrobial Stewardship Interventions in Pediatric Oncology: A Systematic Review.
- Author
-
Muratore E, Baccelli F, Leardini D, Campoli C, Belotti T, Viale P, Prete A, Pession A, Masetti R, and Zama D
- Abstract
Antimicrobial stewardship programs represent efficacious measures for reducing antibiotic overuse and improving outcomes in different settings. Specific data on pediatric oncology are lacking. We conducted a systematic review on the PubMed and Trip databases according to the PRISMA guidelines, searching for reports regarding antimicrobial stewardship in pediatric oncology and hematology patients. The aim of the study was to summarize the present literature regarding the implementation of antimicrobial stewardship programs or initiatives in this particular population, and provide insights for future investigations. Nine papers were included in the qualitative analysis: three regarding antifungal interventions, five regarding antibacterial interventions, and one regarding both antifungal and antibacterial stewardship interventions. Variable strategies were reported among the included studies. Different parameters were used to evaluate the impact of these interventions, including days of therapy per 1000-patient-days, infections with resistant strains, safety analysis, and costs. We generally observed a reduction in the prescription of broad-spectrum antibiotics and an improved appropriateness, with reduced antibiotic-related side effects and no difference in infection-related mortality. Antibiotic stewardship programs or interventions are effective in reducing antibiotic consumption and improving outcomes in pediatric oncology hematology settings, although stewardship strategies differ substantially in different institutions. A standardized approach needs to be implemented in future studies in order to better elucidate the impact of stewardship programs in this category of patients.
- Published
- 2022
- Full Text
- View/download PDF
48. SARS-CoV-2 infection and treatment in a cohort of patients with inborn errors of immunity.
- Author
-
Conti F, Pacillo L, Amodio D, Rivalta B, Moratti M, Campoli C, Zama D, Corsini I, Giancotta C, Bernardi S, Naviglio S, Cicalese MP, Rabusin M, Aiuti A, Cancrini C, Lanari M, Viale P, Palma P, Pession A, and Finocchi A
- Subjects
- Antibodies, Viral, Cohort Studies, Humans, SARS-CoV-2, COVID-19
- Published
- 2022
- Full Text
- View/download PDF
49. Severe neonatal COVID-19: Challenges in management and therapeutic approach.
- Author
-
Marsico C, Capretti MG, Aceti A, Vocale C, Carfagnini F, Serra C, Campoli C, Lazzarotto T, and Corvaglia L
- Subjects
- COVID-19 complications, COVID-19 diagnosis, COVID-19 pathology, Critical Care, Enterobacter isolation & purification, Enterobacteriaceae Infections complications, Enterobacteriaceae Infections diagnosis, Enterobacteriaceae Infections pathology, Enterobacteriaceae Infections therapy, Female, Humans, Infant, Newborn, Lung diagnostic imaging, Lung pathology, Neonatal Sepsis complications, Neonatal Sepsis diagnosis, Neonatal Sepsis pathology, SARS-CoV-2 isolation & purification, Superinfection complications, Superinfection diagnosis, Superinfection pathology, Superinfection therapy, Treatment Outcome, COVID-19 therapy, Neonatal Sepsis therapy
- Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the etiological agent of coronavirus disease 2019 (COVID-19), may manifest as a life-threatening respiratory infection with systemic complications. Clinical manifestations among children are generally less severe than those seen in adults, but critical cases have increasingly been reported in infants less than 1 year of age. We report a severe case of neonatal COVID-19 requiring intensive care and mechanical ventilation, further complicated by a multidrug-resistant Enterobacter asburiae super-infection. Chest X-rays, lung ultrasound, and chest computed tomography revealed extensive interstitial pneumonia with multiple consolidations, associated with persistent increased work of breathing and feeding difficulties. SARS-CoV-2 RNA was detected in respiratory specimens and stools, but not in other biological samples, with a rapid clearance in stools. Serological tests demonstrated a specific SARS-CoV-2 antibody response mounted by the neonate and sustained over time. The therapeutic approach included the use of enoxaparin and steroids which may have contributed to the bacterial complication, underlying the challenges in managing neonatal COVID-19, where the balance between viral replication and immunomodulation maybe even more challenging than in older ages., (© 2021 Wiley Periodicals LLC.)
- Published
- 2022
- Full Text
- View/download PDF
50. A Proof of Concept of the Role of TDM-Based Clinical Pharmacological Advices in Optimizing Antimicrobial Therapy on Real-Time in Different Paediatric Settings.
- Author
-
Gatti M, Cojutti PG, Campoli C, Caramelli F, Corvaglia LT, Lanari M, Pession A, Ramirez S, Viale P, and Pea F
- Abstract
Introduction: Antimicrobial treatment is quite common among hospitalized children. The dynamic age-associated physiological variations coupled with the pathophysiological alterations caused by underlying illness and potential drug-drug interactions makes the implementation of appropriate antimicrobial dosing extremely challenging among paediatrics. Therapeutic drug monitoring (TDM) may represent a valuable tool for assisting clinicians in optimizing antimicrobial exposure. Clinical pharmacological advice (CPA) is an approach based on the correct interpretation of the TDM result by the MD Clinical Pharmacologist in relation to specific underlying conditions, namely the antimicrobial susceptibility of the clinical isolate, the site of infection, the pathophysiological characteristics of the patient and/or the drug-drug interactions of cotreatments. The aim of this study was to assess the role of TDM-based CPAs in providing useful recommendations for the real-time personalization of antimicrobial dosing regimens in various paediatric settings. Materials and methods: Paediatric patients who were admitted to different settings of the IRCCS Azienda Ospedaliero-Universitaria of Bologna, Italy (paediatric intensive care unit [ICU], paediatric onco-haematology, neonatology, and emergency paediatric ward), between January 2021 and June 2021 and who received TDM-based CPAs on real-time for personalization of antimicrobial therapy were retrospectively assessed. Demographic and clinical features, CPAs delivered in relation to different settings and antimicrobials, and type of dosing adjustments were extracted. Two indicators of performance were identified. The number of dosing adjustments provided over the total number of delivered CPAs. The turnaround time (TAT) of CPAs according to a predefined scale (optimal, <12 h; quasi-optimal, between 12-24 h; acceptable, between 24-48 h; suboptimal, >48 h). Results: Overall, 247 CPAs were delivered to 53 paediatric patients (mean 4.7 ± 3.7 CPAs/patient). Most were delivered to onco-haematological patients (39.6%) and to ICU patients (35.8%), and concerned mainly isavuconazole (19.0%) and voriconazole (17.8%). Overall, CPAs suggested dosing adjustments in 37.7% of cases (24.3% increases and 13.4% decreases). Median TAT was 7.5 h (IQR 6.1-8.8 h). Overall, CPAs TAT was optimal in 91.5% of cases, and suboptimal in only 0.8% of cases. Discussion: Our study provides a proof of concept of the helpful role that TDM-based real-time CPAs may have in optimizing antimicrobial exposure in different challenging paediatric scenarios., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2021 Gatti, Cojutti, Campoli, Caramelli, Corvaglia, Lanari, Pession, Ramirez, Viale and Pea.)
- Published
- 2021
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.