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1.
New Microbiol ; 46(4): 395-399, 2024 Jan.
Article in English | MEDLINE | ID: mdl-38252051

ABSTRACT

Candida auris has emerged globally as a multidrug-resistant health care-associated fungal pathogen. In the literature, nosocomial outbreaks are reported worldwide. In addition, C. auris diffusion occurs in high-dependency settings with infections typically affecting critically ill patients, resulting in life-threatening disease. We describe the first documented case of C. auris in northeastern Italy and the measures applied to contain the transmission that led to zero collateral infections.


Subject(s)
Candida auris , Hospitals , Humans , Disease Outbreaks , Italy/epidemiology
2.
Int J Syst Evol Microbiol ; 68(11): 3557-3562, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30204586

ABSTRACT

Two mycobacterial strains with close similarity to the Mycobacterium tuberculosis complex (MTBC) were isolated from cutaneous lesions of patients in the USA and Italy. At the phenotypic level, similarities to the MTBC included slow growth rate, rough morphotype of the unpigmented colonies and nearly identical high-performance liquid chromatography profiles of mycolic acids. In contrast to the MTBC, the strains were niacin- and nitrate-negative, and catalase-positive both at 68 °C and in semi-quantitative tests. The clinical isolates were more closely related to M. tuberculosis than to any other known mycobacterium and scored positive with commercial DNA probes (Hologic AccuProbe M. tuberculosis). Both average nucleotide identity and genome-to-genome distance suggested the strains are different from the MTBC. Therefore, given the distinguishing phenotypic and genomic-scale differences, we submit that the strains belong to a new species we have named Mycobacteriumdecipiens with type strain TBL 1200985T (=ATCC TSD-117T=DSM 105360T).


Subject(s)
Mycobacterium Infections/microbiology , Mycobacterium/classification , Phylogeny , Tuberculosis, Cutaneous/microbiology , Bacterial Typing Techniques , Base Composition , DNA, Bacterial/genetics , Humans , Italy , Mycobacterium/genetics , Mycobacterium/isolation & purification , Mycobacterium tuberculosis , Mycolic Acids/chemistry , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , United States
3.
Biol Blood Marrow Transplant ; 23(2): 333-339, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27826061

ABSTRACT

The objective of this study was to determine risk factors and outcomes of infections by multidrug-resistant gram-negative (MDR GN) bacteria in 241 recipients of hematopoietic stem cell transplantation (HSCT). The cumulative incidence of infections was 10.5% (95% CI, 12.0% to 25.8%), with 57% of infections occurring during the period of severe neutropenia (neutrophil count < .1 × 106/L). In multivariate analysis, allogeneic transplant and colonization with MDR GN bacteria at admission to the transplant unit were significantly associated with an increased risk of infection. Although we observed neither transplant-related mortality (TRM) nor deaths due to infections by MDR GN bacteria after autologous transplant, in the allogeneic setting a significant difference was reported in terms of overall survival (OS) and TRM between patients who developed infections and those who did not (1-year OS, 39% versus 68%; 1-year TRM, 42% versus 19%). In multivariate analysis, refractory disease and development of grades III to IV graft-versus-host disease (GVHD) were factors that affected both TRM and OS, whereas occurrence of infections by MDR GN pathogens significantly reduced OS. We conclude that eligibility to allogeneic HSCT in MDR GN bacteria carriers should be carefully evaluated together with all other factors that independently influence outcome (disease status, donor, and GVHD risk).


Subject(s)
Bone Marrow Transplantation , Gram-Negative Bacterial Infections/epidemiology , Peripheral Blood Stem Cell Transplantation , Adolescent , Adult , Aged , Anti-Bacterial Agents/therapeutic use , Bone Marrow Transplantation/adverse effects , Drug Resistance, Multiple, Bacterial , Female , Follow-Up Studies , Gram-Negative Bacteria/drug effects , Gram-Negative Bacteria/isolation & purification , Gram-Negative Bacterial Infections/drug therapy , Gram-Negative Bacterial Infections/etiology , Humans , Immunocompromised Host , Incidence , Male , Middle Aged , Peripheral Blood Stem Cell Transplantation/adverse effects , Proportional Hazards Models , Retrospective Studies , Risk Assessment , Risk Factors , Treatment Outcome , Young Adult
4.
Article in English | MEDLINE | ID: mdl-28760900

ABSTRACT

We assessed the population pharmacokinetics of high-dose continuous-infusion (HDCI) meropenem in a cohort of patients with Klebsiella pneumoniae carbapenemase (KPC)-producing Klebsiella pneumoniae (KPC-Kp) infections. Monte Carlo simulations were used to define the permissible HDCI meropenem regimens that could be safely considered for the treatment of KPC-Kp infections due to meropenem-resistant strains. Permissible doses were arbitrarily defined as those associated with a ≤10% to 15% likelihood of meropenem steady-state concentrations (Css) of >100 mg/liter. Probabilities of target attainment (PTA) of four incremental pharmacodynamic determinants for meropenem efficacy (100% T>1×MIC, 100% T>2×MIC, 100% T>3×MIC, and 100% T>4×MIC, where "T>MIC" represents the time during which the plasma concentration of this time-dependent antibacterial agent is maintained above the MIC for the pathogen) in relation to different classes of renal function were calculated. The cumulative fractions of response (CFR) for the permissible HDCI meropenem regimens were calculated against the MIC distribution of the KPC-Kp clinical isolates that were collected routinely at our University Hospital between 2013 and 2016 (n = 169). Ninety-seven meropenem Css were included in the analysis. The final model included creatinine clearance (CrCL) as a covariate and explained 94% of the population variability. Monte Carlo simulations based on licensed dosages of up to 6 g/day predicted an acceptable PTA (>80%) of 100% T>1×MIC against KPC-Kp with a meropenem MIC of ≤32 mg/liter in patients with a CrCL level of <130 ml/min. Dosages of 8 g/day were needed for achieving the same target in patients with CrCL at levels of 130 to 200 ml/min. In dealing with pathogens with a meropenem MIC of 64 mg/liter, HDCI regimens using meropenem at higher than licensed levels should be considered. In these cases, real-time therapeutic drug monitoring could be a useful adjunct for optimized care. The predicted CFR were >75% in all of the classes of renal function.


Subject(s)
Anti-Bacterial Agents , Bacteremia/drug therapy , Bacterial Proteins/metabolism , Klebsiella Infections/drug therapy , Klebsiella pneumoniae/drug effects , Thienamycins , beta-Lactamases/metabolism , Adult , Aged , Aged, 80 and over , Anti-Bacterial Agents/blood , Anti-Bacterial Agents/pharmacokinetics , Anti-Bacterial Agents/pharmacology , Bacteremia/microbiology , Creatinine/blood , Drug Monitoring , Humans , Infusions, Intravenous , Klebsiella Infections/microbiology , Klebsiella pneumoniae/metabolism , Meropenem , Microbial Sensitivity Tests , Middle Aged , Monte Carlo Method , Retrospective Studies , Thienamycins/blood , Thienamycins/pharmacokinetics , Thienamycins/therapeutic use
5.
Skeletal Radiol ; 46(6): 777-783, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28299432

ABSTRACT

BACKGROUND: Tuberculous spondylodiscitis can be difficult to diagnose because of its nonspecific symptoms and the similarities with non-tubercular forms of spinal infection. Fluorine-18-fluorodeoxyglucose positron emission tomography combined with computed tomography (FDG PET-CT) is increasingly used for the diagnosis and monitoring of tubercular diseases. METHODS: Retrospective, case-control study comparing tuberculous spondylodiscitis with biopsy-confirmed pyogenic spondylodiscitis in the period 2010-2012. RESULTS: Ten cases of tuberculous spondylodiscitis and 20 controls were included. Compared to pyogenic, tuberculous spondylodiscitis was more frequent in younger patients (P = 0.01) and was more often associated with thoraco-lumbar tract lesions (P = 0.01) and multiple vertebral involvement (P = 0.01). Significantly higher maximum standardized uptake values (SUV) at FDG-PET were displayed by tuberculous spondylodiscitis compared to controls (12.4 vs. 7.3, P = 0.003). SUV levels above 8 showed the highest value of specificity (0.80). Mean SUV reduction of 48% was detected for tuberculous spondylodiscitis at 1-month follow-up. CONCLUSIONS: Higher SUV levels at FDG-PET were detected in tuberculous compared with pyogenic spondylodiscitis. PET-CT use appeared useful in the disease follow-up after treatment initiation.


Subject(s)
Discitis/diagnostic imaging , Discitis/microbiology , Fluorodeoxyglucose F18/pharmacokinetics , Positron-Emission Tomography/methods , Tuberculosis/diagnostic imaging , Bacterial Infections/diagnostic imaging , Case-Control Studies , Diagnosis, Differential , Female , Humans , Intervertebral Disc/diagnostic imaging , Intervertebral Disc/microbiology , Male , Middle Aged , Positron Emission Tomography Computed Tomography , Radiopharmaceuticals/pharmacokinetics , Retrospective Studies , Sensitivity and Specificity
6.
Infection ; 43(3): 361-6, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25808263

ABSTRACT

Differences in clinical characteristics and outcome between elderly (>60 years) and younger (18-59 years) tuberculosis (TB) patients were retrospectively evaluated. Alcohol abuse, radiological evidence of cavitation, and cough at presentation were more frequent among younger patients. Older patients were more likely to have comorbidities, disseminated TB, longer duration of symptoms and higher TB-related mortality (19 vs 0%). Very old patients (≥80 years) showed increased liver toxicity and hospital acquired infections compared to patients aged 60-79 years.


Subject(s)
Antitubercular Agents/therapeutic use , Tuberculosis/drug therapy , Tuberculosis/pathology , Adolescent , Adult , Aged , Aged, 80 and over , Female , Humans , Italy , Male , Middle Aged , Retrospective Studies , Survival Analysis , Tertiary Care Centers , Treatment Outcome , Tuberculosis/mortality , Young Adult
7.
J Clin Microbiol ; 51(4): 1256-9, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23345292

ABSTRACT

In order to assess the frequency of clinically relevant linezolid-resistant staphylococcal isolates, and the role of linezolid in maintaining and coselecting multiple resistance mechanisms (cfr, 23S rRNA, L3/L4 mutations), a prospective Italian study was performed from 2010 to 2011 to confirm the diffusion of three major multidrug-resistant clones (ST2, ST5, ST23).


Subject(s)
Acetamides/pharmacology , Anti-Bacterial Agents/pharmacology , Drug Resistance, Bacterial , Oxazolidinones/pharmacology , Staphylococcal Infections/epidemiology , Staphylococcal Infections/microbiology , Staphylococcus/drug effects , Genes, Bacterial , Humans , Italy/epidemiology , Linezolid , Mutation , Prevalence , Prospective Studies , Staphylococcus/isolation & purification
8.
Healthcare (Basel) ; 11(3)2023 Feb 02.
Article in English | MEDLINE | ID: mdl-36767000

ABSTRACT

Candida auris is considered to be an emerging fungal pathogen and is related to high mortality rates, persistent candidemia, inconsistencies in susceptibility testing results and misidentification by available commercial identification systems. Multidrug-resistant (MDR) and pandrug-resistant (PDR) strains are increasingly detected. In Europe, hospital outbreaks caused by C. auris have been reported in the United Kingdom (UK), Italy and Spain; however, several cases have been sporadically detected in all European countries. C. auris is difficult to control despite enhanced control measures due to its ability to survive for a long time in environments and colonize patients for prolonged periods. An adequate laboratory diagnostic capacity and national surveillance are fundamental to rapidly detect new C. auris cases and to apply the correct measures to circumscribe them and prevent their spread. Our narrative review aims to highlight the primary C. auris outbreaks and case reports that have occurred in Europe.

10.
Eur Respir J ; 40(2): 442-7, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22241741

ABSTRACT

Extrapulmonary tuberculosis (EPTB) accounts for more than 20% of tuberculosis (TB) cases. Xpert MTB/RIF (Xpert) (Cepheid, Sunnyvale, CA, USA) is a fully automated amplification system, for which excellent results in the diagnosis of pulmonary TB in highly endemic countries have been recently reported. We aimed to assess the performance of the Xpert system in diagnosing EPTB in a low incidence setting. We investigated with Xpert a large number of consecutive extrapulmonary clinical specimens (1,476, corresponding to 1,068 patients) including both paediatric (494) and adult samples. We found, in comparison with a reference standard consisting of combination of culture and clinical diagnosis of TB, an overall sensitivity and specificity of 81.3% and 99.8% for Xpert, while the sensitivity of microscopy was 48%. For biopsies, urines, pus and cerebrospinal fluids the sensitivity exceeded 85%, while it was slightly under 80% for gastric aspirates. It was, in contrast, lower than 50% for cavitary fluids. High sensitivity and specificity (86.9% and 99.7%, respectively) were also obtained for paediatric specimens. Although the role of culture remains central in the microbiological diagnosis of EPTB, the sensitivity of Xpert in rapidly diagnosing the disease makes it a much better choice compared to smear microscopy. The ability to rule out the disease still remains suboptimal.


Subject(s)
Diagnostic Techniques and Procedures , Tuberculosis/diagnosis , Tuberculosis/metabolism , Adolescent , Adult , Automation , Biopsy , Child , Child, Preschool , Humans , Infant , Infant, Newborn , Nucleic Acids/metabolism , Reproducibility of Results , Sensitivity and Specificity , Sputum/microbiology , Tuberculosis, Multidrug-Resistant/diagnosis , Tuberculosis, Multidrug-Resistant/metabolism
11.
Infez Med ; 30(3): 454-458, 2022.
Article in English | MEDLINE | ID: mdl-36148162

ABSTRACT

We report the case of successful use of cefiderocol (FDC) in a Carbapenemase Producing K. pneumoniae (CPKP) post-surgical meningitis in a 44-year-old man treated with antimicrobial therapy and external ventricular drainage (EVD). The patient was known for being colonised by CPKP; for this reason, therapy with ceftazidime/avibactam (CZA) plus fosfomycin and linezolid was started. After an initial response a CZA resistant CPKP strain was isolated from CSF culture, so the antibiotic therapy was modified to FDC with trimethoprim/sulfamethoxazole for 14 days, and EVD was replaced. A complete recovery was obtained. This is the first case report describing FDC administration in CPKP meningitis.

12.
Int J Antimicrob Agents ; 60(2): 106611, 2022 Aug.
Article in English | MEDLINE | ID: mdl-35697179

ABSTRACT

Management of patients with infections caused by multidrug-resistant organisms is challenging and requires a multidisciplinary approach to achieve successful clinical outcomes. The aim of this paper is to provide recommendations for the diagnosis and optimal management of these infections, with a focus on targeted antibiotic therapy. The document was produced by a panel of experts nominated by the five endorsing Italian societies, namely the Italian Association of Clinical Microbiologists (AMCLI), the Italian Group for Antimicrobial Stewardship (GISA), the Italian Society of Microbiology (SIM), the Italian Society of Infectious and Tropical Diseases (SIMIT) and the Italian Society of Anti-Infective Therapy (SITA). Population, Intervention, Comparison and Outcomes (PICO) questions about microbiological diagnosis, pharmacological strategies and targeted antibiotic therapy were addressed for the following pathogens: carbapenem-resistant Enterobacterales; carbapenem-resistant Pseudomonas aeruginosa; carbapenem-resistant Acinetobacter baumannii; and methicillin-resistant Staphylococcus aureus. A systematic review of the literature published from January 2011 to November 2020 was guided by the PICO strategy. As data from randomised controlled trials (RCTs) were expected to be limited, observational studies were also reviewed. The certainty of evidence was classified using the GRADE approach. Recommendations were classified as strong or conditional. Detailed recommendations were formulated for each pathogen. The majority of available RCTs have serious risk of bias, and many observational studies have several limitations, including small sample size, retrospective design and presence of confounders. Thus, some recommendations are based on low or very-low certainty of evidence. Importantly, these recommendations should be continually updated to reflect emerging evidence from clinical studies and real-world experience.


Subject(s)
Acinetobacter baumannii , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/therapeutic use , Antimicrobial Stewardship , Carbapenems , Drug Resistance, Multiple, Bacterial , Humans
13.
Assist Inferm Ric ; 29(4): 192-7, 2010.
Article in Italian | MEDLINE | ID: mdl-21409812

ABSTRACT

Blood culture contamination represents a source of frustration for clinicians and microbiologists. Contaminated cultures lead to diagnostic uncertainty and are associated with increased health care costs due to unnecessary treatment and testing. Several strategies have been investigated to decrease contamination rates and numerous approaches to distinguish between clinically significant bacteremia and contamination have been explored. In this review, an overview of blood culture contamination is provided and the potential utility of a variety of approaches to improve both detection and prevention is discussed. Multidisciplinary efforts and multitargeted strategies are required to improve the quality and reliability of blood culture sampling.


Subject(s)
Bacteriological Techniques/standards , Blood Specimen Collection/nursing , Blood/microbiology , Bacteremia/diagnosis , Bacteremia/microbiology , Bacteremia/prevention & control , Blood Specimen Collection/standards , Humans , Risk Factors , Time Factors
14.
Emerg Infect Dis ; 15(9): 1351-8; quiz 1544, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19788801

ABSTRACT

Over the past several years, the prevalence of human disease caused by nontuberculous mycobacteria (NTM) has increased. Whether the increase in cases is real or whether more cases are being recognized remains unclear. Despite a considerable increase in knowledge about NTM infections, they still represent a diagnostic and therapeutic challenge for several reasons: 1) pathogenic isolates may be indistinguishable from contaminant or saprophytic isolates; 2) timely and reliable identification of isolates may depend on proper communication between clinicians and laboratory staff; 3) lack of standardized susceptibility testing makes adoption of tailored therapies unrealistic; and 4) lack of treatment guidelines exposes patients to toxic drugs and disappointing outcomes. Laboratory research and multicenter controlled trials are needed to improve diagnosis and treatment of these infections.


Subject(s)
Immunocompetence , Lymphadenitis , Mycobacterium Infections , Mycobacterium , Skin Diseases, Bacterial , Soft Tissue Infections , Tuberculosis, Osteoarticular , Adult , Animals , Child, Preschool , Humans , Infant , Lymphadenitis/epidemiology , Lymphadenitis/microbiology , Mycobacterium/classification , Mycobacterium/isolation & purification , Mycobacterium/pathogenicity , Mycobacterium Infections/diagnosis , Mycobacterium Infections/epidemiology , Mycobacterium Infections/microbiology , Mycobacterium Infections, Nontuberculous/epidemiology , Mycobacterium Infections, Nontuberculous/microbiology , Mycobacterium marinum/classification , Mycobacterium marinum/isolation & purification , Mycobacterium marinum/pathogenicity , Nontuberculous Mycobacteria/classification , Nontuberculous Mycobacteria/isolation & purification , Nontuberculous Mycobacteria/pathogenicity , Prevalence , Skin Diseases, Bacterial/epidemiology , Skin Diseases, Bacterial/microbiology , Soft Tissue Infections/epidemiology , Soft Tissue Infections/microbiology , Tuberculosis, Osteoarticular/epidemiology , Tuberculosis, Osteoarticular/microbiology
16.
Lancet Infect Dis ; 8(5): 323-34, 2008 May.
Article in English | MEDLINE | ID: mdl-18471777

ABSTRACT

A decline in the prevalence of tuberculosis in the developed world over the past several years has been accompanied by an increase in the rate of mycobacterial disease caused by non-tuberculous mycobacteria. However, it is still unclear whether there is a real increase in prevalence or whether non-tuberculous mycobacterial disease is being recognised more frequently by clinicians in a variety of clinical settings, thus enhancing the competence of microbiologists to detect the more unusual and fastidious mycobacteria. The introduction of liquid media for isolation of mycobacteria coupled with more accurate methods for identification have allowed several new species associated with human disease to be recognised. Despite this progress, several issues related to non-tuberculous mycobacterial infections need to be addressed, including the timely and reliable identification of isolates, standardisation and clinical evaluation of susceptibility testing, and capability to distinguish disease-causing isolates from contaminant or saprophytic species. Treatment regimens for non-tuberculous mycobacterial disease are still largely undefined and outcome remains disappointing despite substantial upgrading in laboratory diagnosis and the availability of new antimicrobials. Treatment success is impaired by the long duration of regimens, side-effects, and drug interactions, which prevent patients from full compliance. We discuss the epidemiological features, clinical syndromes, and developments in the investigation, prevention, and treatment of pulmonary non-tuberculous mycobacterial infections.


Subject(s)
Immunocompromised Host , Lung Diseases/epidemiology , Mycobacterium Infections/epidemiology , Mycobacterium/classification , Phylogeny , Anti-Bacterial Agents/therapeutic use , Diagnosis, Differential , Humans , Lung Diseases/drug therapy , Lung Diseases/microbiology , Lung Diseases/pathology , Mycobacterium/isolation & purification , Mycobacterium Infections/drug therapy , Mycobacterium Infections/microbiology , Mycobacterium Infections/pathology , Prevalence , Treatment Outcome
17.
J Glob Antimicrob Resist ; 14: 238-241, 2018 09.
Article in English | MEDLINE | ID: mdl-29775786

ABSTRACT

OBJECTIVES: The aim of this study was to assess the minimum inhibitory concentration (MIC) distribution for meropenem and other antimicrobials with Gram-negative activity against Klebsiella pneumoniae carbapenemase-producing K. pneumoniae (KPC-Kp) clinical isolates collected at a tertiary hospital in Italy between 2013-2016. METHODS: The antimicrobial susceptibility of KPC-Kp strains was tested by the broth microdilution method using customised 96-well plates and the results were interpreted according to European Committee on Antimicrobial Susceptibility Testing (EUCAST) recommendations. RESULTS: Among 169 consecutive KPC-Kp clinical isolates, 45 (26.6%) were susceptible to meropenem (MIC≤2mg/L). Among the 124 meropenem-resistant isolates, 73 (58.9%) had a meropenem MIC between 16-64mg/L. The overall resistance rate for the other antimicrobials tested was very high both for ciprofloxacin and levofloxacin (99.0%), was moderate for amikacin (37.4%) and was low for gentamicin (11.2%), colistin (8.2%) and tigecycline (7.7%). Aminoglycosides had a dichotomous behaviour in relation to meropenem MIC increase. The resistance rate for gentamicin remained <20% across all meropenem MICs; conversely, that for amikacin increased from <20% in the presence of meropenem MIC≤8mg/L up to ca. 80% in the presence of meropenem MIC≥64mg/L. Resistance rates for tigecycline and colistin remained <20% in the presence of meropenem MICs up to 64mg/L. CONCLUSION: The overall susceptibility rates of antimicrobials with Gram-negative activity may vary greatly among KPC-Kp clinical isolates. A tight relationship between meropenem MIC increase and the resistance rate for amikacin was documented.


Subject(s)
Anti-Bacterial Agents/pharmacology , Carbapenem-Resistant Enterobacteriaceae/drug effects , Klebsiella Infections/microbiology , Klebsiella pneumoniae/drug effects , Meropenem/pharmacology , Ciprofloxacin/pharmacology , Drug Resistance, Bacterial , Humans , Italy , Klebsiella pneumoniae/isolation & purification , Levofloxacin/pharmacology , Microbial Sensitivity Tests , Retrospective Studies , Tertiary Care Centers
18.
Infect Dis Health ; 23(1): 17-22, 2018 03.
Article in English | MEDLINE | ID: mdl-30479299

ABSTRACT

BACKGROUND: Imported malaria cases continue to occur in non-endemic regions among travellers returning from tropical and subtropical countries. At particular risk of acquiring malaria is the group of travellers identified as immigrants who return to their home country with the specific intent of visiting friends or relatives (VFRs) and who commonly believe they are immune to malaria and fail to seek pre-travel advice. Our aim was to review the current trends of imported malaria in the three main hospitals of the Friuli-Venezia Giulia region (FVG), North Eastern Italy, focusing in particular on patient characteristics and laboratory findings. METHODS: In this retrospective study, we examined all malaria cases among patients admitted from January 2010 through December 2014 to the emergency department of the three main hospitals located in FVG. RESULTS: During the 5-year study period from 2010 to 2014, there were a total of 140 patients with a diagnosis of suspected malaria and who received microscopic confirmation of malaria. The most common species identified was P. falciparum, in 96 of 140 cases (69%), followed by P. vivax (13%), P. ovale (4%), P. malariae (4%), and mixed infection (4%). The most common reason for travel was VFRs (54%), followed by work (17%), and recent immigration (15%). Moreover, 78% of all patients took no chemoprophylaxis, 80 (79%) of whom were foreigners. Notably, the percentage of Italian travellers who took chemoprophylaxis was only 20% (8 of 39 Italian cases), and the regimen was appropriate in only four cases. Parasitaemia greater than 5% was observed in 11 cases (10%), all due to P. falciparum infection. CONCLUSIONS: We highlight that VFRs have the highest proportion of malaria morbidity and the importance of improving patient management in this category. These data are useful for establishing appropriate malaria prevention measures and recommendations for international travellers.


Subject(s)
Malaria/epidemiology , Travel , Adolescent , Adult , Aged , Chemoprevention , Child , Female , Hospitals , Humans , Italy/epidemiology , Malaria/ethnology , Malaria/microbiology , Malaria/prevention & control , Male , Middle Aged , Plasmodium falciparum/isolation & purification , Plasmodium vivax/isolation & purification , Retrospective Studies , Travel Medicine , Young Adult
19.
Infect Dis (Lond) ; 50(3): 214-219, 2018 03.
Article in English | MEDLINE | ID: mdl-28988525

ABSTRACT

BACKGROUND: Evaluation of the role on patient mortality exerted by biofilm forming (BF) Candida strains, by using predictive clinical data. METHODS: Eighty-nine strains isolated from Candida bloodstream infection, occurring in two Italian University Hospitals, were employed in this study. A random forest (RF) model was built with a procedure of iterative selection of the risk factors potentially able to predict the probability of death. The similarity between patient conditions and Bayesian clustering was calculated in order to evaluate the role of predictors in the stratification of the death risk. RESULTS: Three different groups of patients with different probability of death were obtained with a RF approach: Group 1 (mortality in 33.3% of cases), Group 2 (death in 50% of cases), and Group 3 (mortality in 76.9% of cases). The comparison between these three groups showed that BF correlated well with increased mortality in patients, admitted for medical diagnosis, with high APACHE II score and treated with azoles. Early treatment within 24 h between candidemia diagnosis and the beginning of antifungal therapy was associated with the lowest of BF rate and mortality. CONCLUSIONS: BF by Candida spp. seems to be clinically associated with increased mortality especially in medical patients with higher Apache II score or treated with azoles.


Subject(s)
Biofilms/growth & development , Candida/physiology , Candidemia/microbiology , Candidemia/mortality , Aged , Aged, 80 and over , Antifungal Agents/therapeutic use , Bayes Theorem , Candida/isolation & purification , Candidemia/diagnosis , Candidemia/drug therapy , Female , Hospitals, University , Humans , Italy , Male , Middle Aged , Predictive Value of Tests , Retrospective Studies , Risk Factors
20.
Intern Emerg Med ; 13(2): 199-204, 2018 03.
Article in English | MEDLINE | ID: mdl-29322386

ABSTRACT

Candida is an increasing cause of bloodstream infection and is associated with significant morbidity and mortality. The aim of our study is to analyze risk factors for short-term mortality in patients with bloodstream Candida spp. infections admitted to Internal Medicine Wards (IMWs). This was a retrospective case-control study between January 2012 and December 2014 from four University Hospitals in Italy, where patients with candidemia dying within 30 days from diagnosis were matched to control cases with candidemia who survived in the same period of time. Two-hundred and fifty cases of candidemia were registered during the 36 months of enrollment. Among these, 112 patients died (45%) within 30 days from the first blood culture's positivity for Candida spp. At multivariate analysis, septic shock [odds ratio (95% CI) = 2.919 (1.62-5.35), p < 0.001] and concomitant chronic kidney failure [odds ratio (95% CI) = 2.296 (1.07-5.12), p = 0.036] were independent predictors of mortality. Low-dose chronic steroid therapy was protective [odds ratio (95% CI) = 0.461 (0.25-0.83), p = 0.011).


Subject(s)
Candidemia/mortality , Critical Illness/therapy , Aged , Aged, 80 and over , Candida/drug effects , Candida/pathogenicity , Candidemia/epidemiology , Chi-Square Distribution , Cohort Studies , Critical Illness/epidemiology , Female , Humans , Internal Medicine/statistics & numerical data , Internal Medicine/trends , Italy/epidemiology , Logistic Models , Male , Middle Aged , Multivariate Analysis , Retrospective Studies , Risk Factors , Statistics, Nonparametric
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