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1.
J Hosp Infect ; 87(1): 59-62, 2014 May.
Article in English | MEDLINE | ID: mdl-24746232

ABSTRACT

A three-year surveillance of non-tuberculous mycobacteria (NTM) in a hospital water distribution system was conducted at a facility located in southern Alberta. NTM was not present in any intake water samples, but was found in 106/183 (58%) of endpoint samples across 15 sites over the study period. Two different species of NTM were identified, Mycobacterium gordonae (88/183) and Mycobacterium avium (34/183); with only one strain of each M. gordonae and M. avium found. Given the sensitive nature of a healthcare facility, attention should be paid to minimize potential impact of NTM from potable water sources on patient health.


Subject(s)
Drinking Water/microbiology , Mycobacterium avium/classification , Mycobacterium avium/isolation & purification , Nontuberculous Mycobacteria/classification , Nontuberculous Mycobacteria/isolation & purification , Alberta , Epidemiological Monitoring , Hospitals , Humans , Mycobacterium avium/genetics , Nontuberculous Mycobacteria/genetics
2.
Food Microbiol ; 32(1): 202-5, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22850394

ABSTRACT

Consumption of foods containing Staphylococcus aureus can cause severe gastro-intestinal illness. Given the fact that over the past decade, Canada has seen increasing rates of methicillin-resistant S. aureus (MRSA) carriage and infection, the objective of this study was to investigate the impact of methicillin-susceptible S. aureus (MSSA) and MRSA on foodborne illness in Alberta, Canada. Between January 2007 and December 2010, there were 693 food samples associated with foodborne investigations submitted to the Alberta Provincial Laboratory for Public Health (ProvLab). These foods were screened for: Bacillus cereus, Clostridium perfringens, S. aureus, Aeromonas spp., Campylobacter spp., Escherichia coli O157:H7, Salmonella, Shigella spp., and Yersinia spp. S. aureus was identified in 10.5% (73/693) of samples, and of these, 59% (43/73) were co-contaminated with at least one other organism on the screening panel. The S. aureus positive samples included 29 meat, 20 prepared foods containing meat, 11 prepared foods not containing meat, 10 dairy, and three produce. Methicillin-resistance was not detected in any isolates tested. These findings indicate that the presence of S. aureus in food associated with foodborne investigations is a cause for concern, and although MRSA was not found, the potential for outbreaks exists, and ongoing surveillance should be sustained.


Subject(s)
Food Contamination/analysis , Foodborne Diseases/microbiology , Methicillin-Resistant Staphylococcus aureus/isolation & purification , Staphylococcal Infections/microbiology , Staphylococcus aureus/isolation & purification , Anti-Bacterial Agents/pharmacology , Canada/epidemiology , Dairy Products/microbiology , Foodborne Diseases/epidemiology , Humans , Meat/microbiology , Meat Products/microbiology , Methicillin-Resistant Staphylococcus aureus/drug effects , Methicillin-Resistant Staphylococcus aureus/genetics , Staphylococcal Infections/epidemiology , Staphylococcus aureus/drug effects , Staphylococcus aureus/genetics
3.
Zoonoses Public Health ; 58(6): 432-9, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21824340

ABSTRACT

Exposure to microorganisms resistant to antimicrobials may constitute a health risk to human populations. It is believed that one route of exposure occurs when people engage in recreational activities in water contaminated with these microorganisms. The main objective of this study was to explore population-level and environmental determinants specifically associated with the presence of antimicrobial resistant (AMR) generic Escherichia coli isolated from recreational waters sampled from beaches located in southern Quebec, Canada. Water samples originated from the Quebec provincial beach surveillance program for the summers of 2004 and 2005. This study focused on three classes of determinants, namely: agricultural, population-level and beach characteristics for a total of 19 specific factors. The study was designed as a retrospective observational analysis and factors were assessed using logistic regression methods. From the multivariable analysis, the data suggested that the percentage of land used for spreading liquid manure was a significant factor associated with the presence of AMR E. coli (OR=27.73). Conceptually, broad factors potentially influencing the presence of AMR bacteria in water must be assessed specifically in addition to factors associated with general microbial contamination. Presence of AMR E. coli in recreational waters from beaches in southern Quebec may represent a risk for people engaging in water activities and this study provides preliminary evidence that agricultural practices, specifically spreading liquid manure in agricultural lands nearby beaches, may be linked to the contamination of these waters by AMR E. coli.


Subject(s)
Agriculture , Bathing Beaches , Escherichia coli/isolation & purification , Lakes/microbiology , Water Microbiology , Animals , Human Activities , Humans , Logistic Models , Quebec , Seasons , Time Factors
4.
Antimicrob Agents Chemother ; 53(7): 3126-30, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19398647

ABSTRACT

A total of 142 cefoxitin-resistant Escherichia coli isolates from water sources were collected across Canada. Multidrug resistance was observed in 65/142 (45.8%) isolates. The bla(CMY-2) gene was identified in 110/142 (77.5%) isolates. Sequencing of the chromosomal ampC promoter region showed mutations from the wild type, previously shown to hyperproduce AmpC. CMY-2-producing plasmids predominantly belonged to replicon groups I1-Igamma, A/C, and K/B. The majority of the E. coli isolates belonged to the nonvirulent phylogenetic groups A and B1.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bathing Beaches , Cefoxitin/pharmacology , Escherichia coli/drug effects , Escherichia coli/genetics , Water Microbiology , Bacterial Proteins/genetics , Canada , Drug Resistance, Bacterial/genetics , Mutation , beta-Lactamases/genetics
5.
Arch Environ Health ; 58(8): 452-63, 2003 Aug.
Article in English | MEDLINE | ID: mdl-15259424

ABSTRACT

The authors assessed the psychological, neuropsychological, and electrocortical effects of human exposure to mixed colonies of toxigenic molds. Patients (N = 182) with confirmed mold-exposure history completed clinical interviews, a symptom checklist (SCL-90-R), limited neuropsychological testing, quantitative electroencephalogram (QEEG) with neurometric analysis, and measures of mold exposure. Patients reported high levels of physical, cognitive, and emotional symptoms. Ratings on the SCL-90-R were "moderate" to "severe," with a factor reflecting situational depression accounting for most of the variance. Most of the patients were found to suffer from acute stress, adjustment disorder, or post-traumatic stress. Differential diagnosis confirmed an etiology of a combination of external stressors, along with organic metabolically based dysregulation of emotions and decreased cognitive functioning as a result of toxic or metabolic encephalopathy. Measures of toxic mold exposure predicted QEEG measures and neuropsychological test performance. QEEG results included narrowed frequency bands and increased power in the alpha and theta bands in the frontal areas of the cortex. These findings indicated a hypoactivation of the frontal cortex, possibly due to brainstem involvement and insufficient excitatory input from the reticular activating system. Neuropsychological testing revealed impairments similar to mild traumatic brain injury. In comparison with premorbid estimates of intelligence, findings of impaired functioning on multiple cognitive tasks predominated. A dose-response relationship between measures of mold exposure and abnormal neuropsychological test results and QEEG measures suggested that toxic mold causes significant problems in exposed individuals. Study limitations included lack of a comparison group, patient selection bias, and incomplete data sets that did not allow for comparisons among variables.


Subject(s)
Environmental Exposure/adverse effects , Fungi , Mycotoxicosis , Neurotoxicity Syndromes , Adult , Analysis of Variance , Chronic Disease , Cognition Disorders/diagnosis , Cognition Disorders/etiology , Diagnosis, Differential , Electroencephalography , Environmental Exposure/analysis , Environmental Monitoring , Female , Humans , Intelligence Tests , Interview, Psychological , Male , Mental Disorders/diagnosis , Mental Disorders/etiology , Mycotoxicosis/diagnosis , Mycotoxicosis/etiology , Neuropsychological Tests , Neurotoxicity Syndromes/diagnosis , Neurotoxicity Syndromes/etiology , Predictive Value of Tests , Psychiatric Status Rating Scales , Retrospective Studies , Selection Bias , Severity of Illness Index , Stress, Psychological/diagnosis , Stress, Psychological/etiology , Surveys and Questionnaires
6.
J Clin Psychiatry ; 45(3 Pt 2): 47-53, 1984 Mar.
Article in English | MEDLINE | ID: mdl-6321454

ABSTRACT

Sixty patients with chronic pain of the low back or cervical spine concomitant with clinical depression were studied in a 6-week, randomized, double-blind comparison of doxepin and placebo. Significant improvements in the doxepin-treated group compared to placebo or to baseline values were seen on Hamilton depression scores, Global Assessment Scale scores, pain severity, percent of time pain felt, and effect of pain on activity, sleep, and muscle tension. Some improvements were observed after 1 week of treatment; the most improvement occurred at 6 weeks, when the mean doxepin dosage was approximately 200 mg/day and plasma doxepin and nordoxepin averaged 80 ng/ml. No significant harmful effects were observed. Neither plasma beta-endorphin nor enkephalin-like activity demonstrated significant differences from baseline. These data indicate that doxepin is a valuable treatment for patients with chronic pain and depression.


Subject(s)
Depressive Disorder/drug therapy , Doxepin/therapeutic use , Pain/drug therapy , Chronic Disease , Clinical Trials as Topic , Depressive Disorder/complications , Depressive Disorder/psychology , Double-Blind Method , Doxepin/administration & dosage , Doxepin/blood , Endorphins/blood , Enkephalins/blood , Female , Humans , Male , Middle Aged , Pain/complications , Pain/psychology , Placebos , Psychiatric Status Rating Scales , Random Allocation , Time Factors , beta-Endorphin
7.
J Clin Psychiatry ; 43(8 Pt 2): 22-7, 1982 Aug.
Article in English | MEDLINE | ID: mdl-6284720

ABSTRACT

Thirty patients with chronic low back or cervical pain combined with clinical depression were studied in a six-week, randomized, double-blind comparison of doxepin and placebo. Dependent variables included Hamilton Depression Scores, the Clinical Global Assessment Scale, and Profile of Mood States (POMS), and subjective ratings (visual analogue scales) of pain severity, percent of time pain felt, and effect of pain on activity, muscle tension, sleep, mood, and analgesic drug consumption. Plasma levels of doxepin, desmethyldoxepin, beta-endorphin, and enkephalin-like activity were also measured. Significant improvements in the doxepin-treated group compared to the placebo group were seen in Hamilton scores, Global Assessment Scale, Profile of Mood States, percent of time pain felt, and effect of pain on sleep, muscle tension, and mood. Some improvement was observed after 1 week, although most improvement occurred at 6 weeks, when the mean doxepin dose was 2.5 mg/kg and plasma doxepin and desmethyldoxepin averaged 70 ng/ml. Nonspecific enkephalin-like activity (but not beta-endorphins) increased for the treatment group and decreased for the placebo group. The efficacy of doxepin compared with that of placebo was thus documented in several depressive and pain parameters, indicating that doxepin is a valuable treatment for patients with chronic pain and depression.


Subject(s)
Depression/drug therapy , Doxepin/therapeutic use , Endorphins/blood , Enkephalins/blood , Pain/drug therapy , Adult , Aged , Chronic Disease , Depression/complications , Double-Blind Method , Doxepin/analogs & derivatives , Doxepin/blood , Female , Humans , Male , Middle Aged , Pain/complications , Pain/physiopathology , Placebos , Random Allocation , Sensory Thresholds , Sleep , beta-Endorphin
8.
Anesth Analg ; 60(10): 752-5, 1981 Oct.
Article in English | MEDLINE | ID: mdl-7027827

ABSTRACT

Injections of local anesthetics, saline, "dry needling," or other stimuli at specific, tender loci (trigger or acupuncture points) are reportedly efficacious in treatment of chronic pain syndromes. In a randomized, double-blind crossover study, subjective responses of 15 patients with myofascial syndrome to trigger-point injections of either bupivacaine 0.5%, etidocaine 1%, or physiologic saline without preservative were compared. Responses in six pain-related categories were determined before treatment and 15 minutes, 24 hours, and 7 days after treatment. Trigger-point injections with bupivacaine and etidocaine were generally preferred over saline in several pain-tested categories. Implications and possible mechanisms are discussed.


Subject(s)
Acetanilides , Bupivacaine , Etidocaine , Myofascial Pain Syndromes/physiopathology , Pain Management , Sodium Chloride/therapeutic use , Acetanilides/administration & dosage , Bupivacaine/administration & dosage , Clinical Trials as Topic , Double-Blind Method , Etidocaine/administration & dosage , Humans , Injections , Random Allocation , Sodium Chloride/administration & dosage
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