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1.
AIDS Behav ; 20(5): 1116-22, 2016 05.
Article in English | MEDLINE | ID: mdl-26350637

ABSTRACT

Food rations are increasingly offered as part of HIV programs in resource-poor settings, often targeted solely to those with under-nutrition by low body mass index (BMI). This practice does not consider food insecurity, another important risk factor for poor outcomes in people living with HIV/AIDS (PLWH). We analyzed factors associated with low BMI and severe food insecurity in 523 PLWH receiving antiretroviral therapy in rural Haiti using logistic regression. Food insecurity was present in 89 % of individuals. Among those with severe food insecurity, 86 % had a BMI ≥ 18.5 kg/m(2). Severe food insecurity was associated with illiteracy [adjusted odds ratio (AOR) 1.79, p = 0.005], having no income (AOR 1.58, p = 0.04), and poverty (p < 0.001). Compared with those with little to no food insecurity, individuals with severe food insecurity had a less diverse diet. We found that food insecurity was highly prevalent in PLWH receiving antiretroviral therapy in rural Haiti. Using BMI as a sole criterion for food supplementation in HIV programs can exclude highly vulnerable individuals who may benefit from such support.


Subject(s)
Antiretroviral Therapy, Highly Active , Body Mass Index , Diet , Food Supply , HIV Infections/complications , Nutritional Status , Adolescent , Diet/ethnology , Diet/psychology , Food Supply/economics , HIV Infections/drug therapy , HIV Infections/ethnology , Haiti , Humans , Income , Male , Malnutrition/etiology , Poverty Areas , Prevalence , Randomized Controlled Trials as Topic , Risk Factors , Rural Population , Socioeconomic Factors , Young Adult
2.
Clin Infect Dis ; 58(7): 980-3, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24577290

ABSTRACT

This proof-of-concept study demonstrates that no longer routinely reporting urine culture results from noncatheterized medical and surgical inpatients can greatly reduce unnecessary antimicrobial therapy for asymptomatic bacteriuria without significant additional laboratory workload. Larger studies are needed to confirm the generalizability, safety, and sustainability of this model of care.


Subject(s)
Anti-Infective Agents/therapeutic use , Asymptomatic Infections , Bacteriuria/drug therapy , Unnecessary Procedures , Urinary Tract Infections/drug therapy , Aged , Anti-Infective Agents/administration & dosage , Bacteriuria/diagnosis , Drug Therapy/statistics & numerical data , Female , Humans , Inpatients , Male , Urinary Tract Infections/diagnosis
3.
Microbiol Spectr ; 12(5): e0322323, 2024 May 02.
Article in English | MEDLINE | ID: mdl-38526086

ABSTRACT

Gram-negative metallo-ß-lactamase-producing bacteria can be extremely problematic, especially when found to be extensively drug-resistant (XDR). Cefiderocol is a novel antimicrobial that has been shown to overcome most carbapenemases, with very rare resistance reported to date. Within our institution, two multidrug-resistant and one XDR strains were isolated from a patient who recently emigrated from India. Each isolate underwent whole-genome sequencing to resolve plasmids and determine phylogenetics, strain typing, and mechanisms of resistance. The XDR E. coli was ST167, harbored NDM-5, cirA and PBP3 mutations, consistent with cefiderocol resistance. Our study suggests that the NDM region is required in conjunction with cirA and PBP3 mutations. It is not clear why; however, our study did determine a potential novel iron-transport region unique to the cefiderocol-resistant isolate. This is the first characterized cefiderocol-resistant E.coli reported from Canada. Health centers should be on alert for this clone.IMPORTANCEThe development of cefiderocol, a novel siderophore cephalosporin, has provided additional options to the treatment of extensively drug-resistant (XDR) Gram-negative bacteria. Resistance to cefiderocol is poorly understood and only recently described. Here, we describe a case of a patient with recent travel to India harboring three Escherichia coli isolates, one resistant and two susceptible to cefiderocol. Two isolates are highly similar genetically, allowing the mechanism of resistance to be described more closely. The importance of this manuscript contributes both globally to the understanding of cefiderocol resistance in E. coli as well as nationally as this is the first resistant case reported in Canada. This is especially concerning as cefiderocol is not currently approved in Canada. The implications of reporting emerging resistance to new antimicrobials for XDR Gram negatives are impactful to infectious disease specialists, clinical microbiologists, physicians, and public health.


Subject(s)
Anti-Bacterial Agents , Drug Resistance, Multiple, Bacterial , Escherichia coli Infections , Humans , Male , Anti-Bacterial Agents/pharmacology , beta-Lactamases/genetics , beta-Lactamases/metabolism , Canada , Cefiderocol , Cephalosporins/pharmacology , Drug Resistance, Multiple, Bacterial/genetics , Escherichia coli/genetics , Escherichia coli/drug effects , Escherichia coli/isolation & purification , Escherichia coli Infections/microbiology , Escherichia coli Infections/drug therapy , Escherichia coli Proteins/genetics , Escherichia coli Proteins/metabolism , India , Microbial Sensitivity Tests , Mutation , Phylogeny , Plasmids/genetics , Whole Genome Sequencing , Aged
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