Francesco Bruno
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Francesco Bruno has a total of 29 co-authors. Here are the top co-authors by number of shared publications:
- Filomena Puntillo
Department of Interdisciplinary Medicine,University of Bari Aldo Moro,Bari,Italy, Italy
3 shared publications - Caterina Coretti
Department of Biomedical Science and Human Oncology, Hygiene Section, University of Bari “Aldo Moro”, Bari, Italy
2 shared publications - Giuseppina Caggiano
Interdisciplinary Department of Medicine, University of Bari Aldo Moro, 70124 Bari, Italy
2 shared publications - Ilaria Alicino
Anaesthesia and Intensive Care Unit, Department of Emergency and Organ Transplantation, University of Bari, Piazza G. Cesare 11, Bari 70124, Italy
2 shared publications - Maria Teresa Montagna
Interdisciplinary Department of Medicine, Hygiene Section, University of Bari Aldo Moro, 70124 Bari, Italy
2 shared publications - Mariateresa Giglio
Department of Interdisciplinary Medicine,University of Bari Aldo Moro,Bari,Italy, Italy
2 shared publications
Latest Publications
- Open Access
- 1 January 2019
- Published by Elsevier in Annals of Intensive Care
- Vol. 9 (1) , 1-10
High-flow oxygen therapy in tracheostomized patients at high risk of weaning failure
- 1 January 2019
- Published by Elsevier in Annals of Intensive Care
- Vol. 9 (1) , 1-10
Open AccessHigh-flow oxygen therapy in tracheostomized patients at high risk of weaning failure
- 1 January 2014
- Published by American Psychological Association (APA)
Caregiver Self-Administered Questionnaire
- 1 January 2014
- Published by American Psychological Association (APA)
Caregiver Self-Administered Questionnaire
- Open Access
- 10 April 2012
- Published by Springer Nature in Critical Care
- Vol. 16 (2) , R57
Oral nystatin prophylaxis in surgical/trauma ICU patients: a randomised clinical trial
Introduction: Candida prophylaxis in ICU is still a matter of debate. Oral chemoprophylaxis has been advocated to reduce the incidence of Candida colonisation and infection. Methods: We performed a randomised trial studying a single drug (nystatin) versus control in surgical/trauma ICU patients. Multiple-site testing for fungi was performed in each patient on ICU admission (T0) and subsequently every 3 days (T3, T6, T9, and so forth). The primary evaluation criterion was the time course of the corrected colonisation index. Results: Ninety-nine patients were enrolled. At admission, 69 patients exhibited Candida colonisation: the most frequently colonised body sites were the stomach and the pharynx. The most frequent isolated species was Candida albicans. The corrected colonisation index was similar in the two groups at T0 (P = 0.36), while a significant statistical difference was observed between the treatment and control groups at T6 (median 0.14 and 0.33, respectively; P = 0.0016), at T9 (median 0.00 and 0.28, respectively; P = 0.0001), at T12 (median 0.00 and 0.41, respectively; P = 0.0008), and at T15 (median 0.00 and 0.42, respectively; P < 0.0003). The same results were obtained in the subgroup of patients already colonised at ICU admission. Conclusion: This trial shows that nystatin prophylaxis significantly reduces fungal colonisation in surgical/trauma ICU patients, even if already colonised. Trial registration: ClinicalTrials.gov: NCT01495039
- 10 April 2012
- Published by Springer Nature in Critical Care
- Vol. 16 (2) , R57
Open AccessOral nystatin prophylaxis in surgical/trauma ICU patients: a randomised clinical trial
Introduction: Candida prophylaxis in ICU is still a matter of debate. Oral chemoprophylaxis has been advocated to reduce the incidence of Candida colonisation and infection. Methods: We performed a randomised trial studying a single drug (nystatin) versus control in surgical/trauma ICU patients. Multiple-site testing for fungi was performed in each patient on ICU admission (T0) and subsequently every 3 days (T3, T6, T9, and so forth). The primary evaluation criterion was the time course of the corrected colonisation index. Results: Ninety-nine patients were enrolled. At admission, 69 patients exhibited Candida colonisation: the most frequently colonised body sites were the stomach and the pharynx. The most frequent isolated species was Candida albicans. The corrected colonisation index was similar in the two groups at T0 (P = 0.36), while a significant statistical difference was observed between the treatment and control groups at T6 (median 0.14 and 0.33, respectively; P = 0.0016), at T9 (median 0.00 and 0.28, respectively; P = 0.0001), at T12 (median 0.00 and 0.41, respectively; P = 0.0008), and at T15 (median 0.00 and 0.42, respectively; P < 0.0003). The same results were obtained in the subgroup of patients already colonised at ICU admission. Conclusion: This trial shows that nystatin prophylaxis significantly reduces fungal colonisation in surgical/trauma ICU patients, even if already colonised. Trial registration: ClinicalTrials.gov: NCT01495039
- Open Access
- 20 October 2011
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 12 (10) , 7038-7047
Candida Colonization Index in Patients Admitted to an ICU
Multiple-site colonization with Candida spp is commonly recognized as a risk factor for invasive fungal infection in critically ill patients. We carried out a study to determine the relationship between Candida colonization and invasive infection in neurological patients admitted to an ICU. At admission (T0) and every three days for two weeks, different samples (pharynx swab, tracheal secretions, stomach contents, etc.) were collected for mycological surveillance. Candida mannan antigen and Candida anti-mannan antibodies were assayed. The Colonization Index (CI) and Corrected Colonization Index were calculated for each time point. Of all patients 70% was already colonized by Candida spp at T0 and six of them had CI ≥0.5. Three patients developed candidemia; they had CI ≥0.5 before infection. Positive values of Candida mannan antigen and anti-mannan antibodies were found only in the patients with candidemia. The sensitivity and specificity of the Candida mannan test were 66.6% and 100%, respectively, while the sensitivity and specificity of the anti-mannan antibody test were 100%. In accordance with other authors, we find the surveillance cultures are useful to monitor the Candida colonization in ICU patients. In addition, the sequential observation of anti-mannan antibodies could contribute to early diagnosis of candidiasis more than Candida mannan antigen in immunocompetent patients.
- 20 October 2011
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 12 (10) , 7038-7047
Open AccessCandida Colonization Index in Patients Admitted to an ICU
Multiple-site colonization with Candida spp is commonly recognized as a risk factor for invasive fungal infection in critically ill patients. We carried out a study to determine the relationship between Candida colonization and invasive infection in neurological patients admitted to an ICU. At admission (T0) and every three days for two weeks, different samples (pharynx swab, tracheal secretions, stomach contents, etc.) were collected for mycological surveillance. Candida mannan antigen and Candida anti-mannan antibodies were assayed. The Colonization Index (CI) and Corrected Colonization Index were calculated for each time point. Of all patients 70% was already colonized by Candida spp at T0 and six of them had CI ≥0.5. Three patients developed candidemia; they had CI ≥0.5 before infection. Positive values of Candida mannan antigen and anti-mannan antibodies were found only in the patients with candidemia. The sensitivity and specificity of the Candida mannan test were 66.6% and 100%, respectively, while the sensitivity and specificity of the anti-mannan antibody test were 100%. In accordance with other authors, we find the surveillance cultures are useful to monitor the Candida colonization in ICU patients. In addition, the sequential observation of anti-mannan antibodies could contribute to early diagnosis of candidiasis more than Candida mannan antigen in immunocompetent patients.