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Antifungal susceptibility of Candida isolates at one institution 2014 National Cerebral and Cardiovascular Center.
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Print(0)
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Journal Article
Periodical, Full
Medical mycology journal
Periodical, Abbrev.
Med.Mycol.J.
Pub Date Free Form
Volume
55
Issue
1
Start Page
E1
Other Pages
7
Notes
JID: 101562838; 0 (Antifungal Agents); 0 (Echinocandins); 0 (Lipopeptides); 304NUG5GF4 (Itraconazole); 7XU7A7DROE (Amphotericin B); 8VZV102JFY (Fluconazole); D83282DT06 (Flucytosine); JFU09I87TR (Voriconazole); R10H71BSWG (micafungin); ppublish
Place of Publication
Japan
ISSN/ISBN
1882-0476
Accession Number
PMID: 24682093
Language
eng
SubFile
Journal Article; IM
DOI
DN/JST.JSTAGE/mmj/55.E1 [pii]
Output Language
Unknown(0)
PMID
24682093
Abstract
Species distribution and antifungal susceptibility of Candida isolates at one institution were evaluated. Detection rates of fungi were examined for 5 years between 2007 and 2011. Sensitivities of fungi to amphotericin B, flucytosine, fluconazole, micafungin, itraconazole, and voriconazole were evaluated in blood culture-positive patients. A total of 3,832 fungal isolates were detected, including Candida albicans 66.5%, Candida glabrata 20.3%, Candida parapsilosis 6.2%, Candida tropicalis 5.5%, and others 1.5%. Candidemia was diagnosed in 131 patients, and C. albicans, C. parapsilosis, C. glabrata, C. tropicalis, and others were present in 42.0%, 27.5%, 16.0%, 8.4%, and 6.1% of these patients, respectively. Voriconazole had the lowest MIC90s against C. albicans and C. parapsilosis (0.015 and 0.25). Micafungin had a low MIC90 against C. glabrata and C. tropicalis. C. albicans was the most common fungus in patients with candidemia. Voriconazole and micafungin were effective against C. albicans. Amphotericin B was effective for C. parapsilosis, and micafungin showed good efficacy against C. glabrata and C. tropicalis.
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Authors
Katsuragi,S., Sata,M., Kobayashi,Y., Miyoshi,T., Yamashita,Y., Neki,R., Horiuchi,C., Yamanaka,K., Kamiya,C., Iwanaga,N., Tanaka,H., Ikeda,T., Yoshimatsu,J.
Original/Translated Title
URL
Date of Electronic
PMCID
Editors
Nonmedical use of prescription opioids and stimulants among student pharmacists 2009 National Development and Research Institutes, Inc, New York, USA. lord@ndri.org
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of the American Pharmacists Association : JAPhA
Periodical, Abbrev.
J.Am.Pharm.Assoc.(2003)
Pub Date Free Form
Jul-Aug
Volume
49
Issue
4
Start Page
519
Other Pages
528
Notes
LR: 20151119; JID: 101176252; 0 (Analgesics, Opioid); 0 (Central Nervous System Stimulants); 0 (Prescription Drugs); ppublish
Place of Publication
United States
ISSN/ISBN
1544-3450; 1086-5802
Accession Number
PMID: 19589764
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1331/JAPhA.2009.08027 [doi]
Output Language
Unknown(0)
PMID
19589764
Abstract
OBJECTIVES: To examine the prevalence and patterns of nonmedical use of prescription opioid analgesics and stimulants among student pharmacists. DESIGN: Descriptive, nonexperimental, cross-sectional study. SETTING: Private urban college of pharmacy in the United States in fall 2006. PARTICIPANTS: 1,538 PharmD students. INTERVENTION: Online survey. MAIN OUTCOME MEASURES: Lifetime and past-year nonmedical prescription opioid and stimulant use. RESULTS: Response rate for the survey was 62%. Lifetime prevalence of opioid misuse was 8%, and 5% of students had misused in the past year. Lifetime prevalence of stimulant misuse was 7%, and 5% had misused in the past year. Whites and fraternity or sorority members were more likely than their peers to have ever misused opioids. Past-year opioid misuse was more likely among whites, men, and low academic achievers compared with their peers. Lifetime stimulant misuse was more likely among students who were white, older, and fraternity or sorority members, while past-year misuse was more likely among whites and low academic achievers. Common motives for opioid misuse were to have fun, to relax, and to deal with chronic pain. Stimulants were used to improve concentration and academic performance. Friends were the most common source of prescription opioids and stimulants. Nonmedical prescription use was associated with greater likelihood of alcohol and other illicit substance use. CONCLUSION: The prevalence of prescription medication misuse among student pharmacists was lower than (opioids) or comparable with (stimulants) reported rates in college populations. Subgroups of students demonstrated higher rates of nonmedical use, including whites, students involved with fraternities or sororities, and low academic achievers. That friends were the primary source of misused medications indicates that diversion of prescription-only controlled substances likely occurs among student pharmacists. Nonmedical prescription medication use should be considered in the context of other substance use.
Descriptors
Adolescent, Adult, Alcohol Drinking/epidemiology, Analgesics, Opioid, Attention/drug effects, Central Nervous System Stimulants, Cross-Sectional Studies, Educational Status, European Continental Ancestry Group/statistics & numerical data, Female, Health Surveys, Humans, Male, Opioid-Related Disorders/epidemiology/ethnology, Pain/drug therapy, Peer Group, Prescription Drugs, Prevalence, Recreation, Risk Factors, Schools, Pharmacy/statistics & numerical data, Sex Factors, Smoking/epidemiology, Students, Pharmacy/statistics & numerical data, Substance-Related Disorders/epidemiology/ethnology, Surveys and Questionnaires, United States/epidemiology, Young Adult
Links
Book Title
Database
Publisher
Data Source
Authors
Lord,S., Downs,G., Furtaw,P., Chaudhuri,A., Silverstein,A., Gammaitoni,A., Budman,S.
Original/Translated Title
URL
Date of Electronic
PMCID
Editors
Highly sensitive determination of polycyclic aromatic hydrocarbons in ambient air dust by gas chromatography-mass spectrometry after molecularly imprinted polymer extraction 2010 National Environmental Engineering Research Institute, Nehru Marg, Nagpur 440 020, India. rj_krupadam@neeri.res.in
Source Type
Print(0)
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Journal Article
Periodical, Full
Analytical and bioanalytical chemistry
Periodical, Abbrev.
Anal.Bioanal Chem.
Pub Date Free Form
Aug
Volume
397
Issue
7
Start Page
3097
Other Pages
3106
Notes
LR: 20160512; JID: 101134327; 0 (Air Pollutants); 0 (Dust); 0 (Methacrylates); 0 (Polycyclic Hydrocarbons, Aromatic); 0 (Polymers); 0 (Polyvinyls); 0 (poly(vinylpyridine-ethylene dimethacrylate)); 2010/03/05 [received]; 2010/05/18 [accepted]; 2010/05/14 [
Place of Publication
Germany
ISSN/ISBN
1618-2650; 1618-2642
Accession Number
PMID: 20526768
Language
eng
SubFile
Evaluation Studies; Journal Article; IM
DOI
10.1007/s00216-010-3858-6 [doi]
Output Language
Unknown(0)
PMID
20526768
Abstract
A method based on solid--phase extraction with a molecularly imprinted polymer (MIP) has been developed to determine five probable human carcinogenic polycyclic aromatic hydrocarbons (PAHs) in ambient air dust by gas chromatography-mass spectrometry (GC-MS). Molecularly imprinted poly(vinylpyridine-co-ethylene glycol dimethacrylate) was chosen as solid-phase extraction (SPE) material for PAHs. The conditions affecting extraction efficiency, for example surface properties, concentration of PAHs, and equilibration times were evaluated and optimized. Under optimum conditions, pre-concentration factors for MIP-SPE ranged between 80 and 93 for 10 mL ambient air dust leachate. PAHs recoveries from MIP-SPE after extraction from air dust were between 85% and 97% and calibration graphs of the PAHs showed a good linearity between 10 and 1000 ng L(-1) (r = 0.99). The extraction efficiency of MIP for PAHs was compared with that of commercially available SPE materials--powdered activated carbon (PAC) and polystyrene-divinylbenzene resin (XAD)--and it was shown that the extraction capacity of the MIP was better than that of the other two SPE materials. Organic matter in air dust had no effect on MIP extraction, which produced a clean extract for GC-MS analysis. The detection limit of the method proposed in this article is 0.15 ng L(-1) for benzo[a]pyrene, which is a marker molecule of air pollution. The method has been applied to the determination of probable carcinogenic PAHs in air dust of industrial zones and satisfactory results were obtained.
Descriptors
Adsorption, Air Pollutants/analysis, Dust/analysis, Gas Chromatography-Mass Spectrometry/methods, Limit of Detection, Methacrylates/chemistry, Molecular Imprinting, Polycyclic Hydrocarbons, Aromatic/analysis/isolation & purification, Polymers/chemistry, Polyvinyls/chemistry, Solid Phase Extraction/instrumentation/methods
Links
Book Title
Database
Publisher
Data Source
Authors
Krupadam,R. J., Bhagat,B., Khan,M. S.
Original/Translated Title
URL
Date of Electronic
20100606
PMCID
Editors
Benzene, toluene and xylene (BTX) pollution in ambient air: a case study 2004 National Envrionmental Engineering Research Institute, Nagpur.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of environmental science & engineering
Periodical, Abbrev.
J.Environ.Sci.Eng.
Pub Date Free Form
Jan
Volume
46
Issue
1
Start Page
15
Other Pages
20
Notes
LR: 20131121; JID: 101273917; 0 (Air Pollutants); 0 (Vehicle Emissions); 0 (Xylenes); 3FPU23BG52 (Toluene); J64922108F (Benzene); ppublish
Place of Publication
India
ISSN/ISBN
Accession Number
PMID: 16649588
Language
eng
SubFile
Journal Article; IM
DOI
Output Language
Unknown(0)
PMID
16649588
Abstract
Volatile Organic Compounds (VOCs) in presence of sunlight and oxides of nitrogen in atmosphere are considered as precursors for ozone production at the ground level. Concentration of Benzene, Toluene and Xylene (BTX) in ambient air was measured near seven traffic junctions in the city of Nagpur. Air samples were collected using Organic Vapour Sampler and analyzed by Gas Chromatograph equipped with Flame Ionization Detector (FID). Benzene concentration was found to be in the range 9.3 to 28.7 microg/m3, Toluene 3.26 to 21.0 microg/m3 and Xylene 4.9 to 15.0 microg/m3. These values are lower than those found in Metropolitan cities like Mumbai.
Descriptors
Air Pollutants/analysis, Air Pollution/analysis, Benzene/analysis, Cities, Environmental Monitoring, India, Toluene/analysis, Vehicle Emissions, Xylenes/analysis
Links
Book Title
Database
Publisher
Data Source
Authors
Deole,S., Phadke,K. M., Kumar,A.
Original/Translated Title
URL
Date of Electronic
PMCID
Editors
Tribromopyrrole, brominated acids, and other disinfection byproducts produced by disinfection of drinking water rich in bromide 2003 National Exposure Research Laboratory, U.S. Environmental Protection Agency, Athens, Georgia 30605, USA. richardson.susan@epa.gov
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Environmental science & technology
Periodical, Abbrev.
Environ.Sci.Technol.
Pub Date Free Form
1-Sep
Volume
37
Issue
17
Start Page
3782
Other Pages
3793
Notes
LR: 20121115; JID: 0213155; 0 (Bromides); 0 (Chlorine Compounds); 0 (Oxides); 0 (Pyrroles); 8061YMS4RM (chlorine dioxide); ppublish
Place of Publication
United States
ISSN/ISBN
0013-936X; 0013-936X
Accession Number
PMID: 12967096
Language
eng
SubFile
Journal Article; IM
DOI
Output Language
Unknown(0)
PMID
12967096
Abstract
Using gas chromatography/mass spectrometry (GC/MS), we investigated the formation of disinfection byproducts (DBPs) from high bromide waters (2 mg/L) treated with chlorine or chlorine dioxide used in combination with chlorine and chloramines. This study represents the first comprehensive investigation of DBPs formed by chlorine dioxide under high bromide conditions. Drinking water from full-scale treatment plants in Israel was studied, along with source water (Sea of Galilee) treated under carefully controlled laboratory conditions. Select DBPs (trihalomethanes, haloacetic acids, aldehydes, chlorite, chlorate, and bromate) were quantified. Many of the DBPs identified have not been previously reported, and several of the identifications were confirmed through the analysis of authentic standards. Elevated bromide levels in the source water caused a significant shift in speciation to bromine-containing DBPs; bromoform and dibromoacetic acid were the dominant DBPs observed, with very few chlorine-containing compounds found. Iodo-trihalomethanes were also identified, as well as a number of new brominated carboxylic acids and 2,3,5-tribromopyrrole, which represents the first time a halogenated pyrrole has been reported as a DBP. Most of the bromine-containing DBPs were formed during pre-chlorination at the initial reservoir, and were not formed by chlorine dioxide itself. An exception wasthe iodo-THMs, which appeared to be formed by a combination of chlorine dioxide with chloramines or chlorine (either added deliberately or as an impurity in the chlorine dioxide). A separate laboratory study was also conducted to quantitatively determine the contribution of fulvic acids and humic acids (from isolated natural organic matter in the Sea of Galilee) as precursor material to several of the DBPs identified. Results showed that fulvic acid plays a greater role in the formation of THMs, haloacetic acids, and aldehydes, but 2,3,5-tribromopyrrole was produced primarily from humic acid. Because this was the first time a halopyrrole has been identified as a DBP, 2,3,5-tribromopyrrole was tested for mammalian cell cytotoxicity and genotoxicity. In comparison to other DBPs, 2,3,5-tribromopyrrole was 8x, 4.5x, and 16x more cytotoxic than dibromoacetic acid, 3-chloro-4-(dichloromethyl)-5-hydroxy-2-[5H]-furanone [MX], and potassium bromate, respectively. 2,3,5-Tribromopyrrole also induced acute genomic damage, with a genotoxic potency (299 microM) similar to that of MX.
Descriptors
Bromides/analysis/chemistry, Chlorine Compounds/chemistry, Disinfection, Environmental Monitoring, Gas Chromatography-Mass Spectrometry, Oxides/chemistry, Pyrroles/chemistry, Risk Assessment, Water Supply
Links
Book Title
Database
Publisher
Data Source
Authors
Richardson,S. D., Thruston,A. D.,Jr, Rav-Acha,C., Groisman,L., Popilevsky,I., Juraev,O., Glezer,V., McKague,A. B., Plewa,M. J., Wagner,E. D.
Original/Translated Title
URL
Date of Electronic
PMCID
Editors
Mobile phone-based interventions for smoking cessation 2016 National Institute for Health Innovation, University of Auckland, Tamaki Campus, Private Bag 92019, Auckland, New Zealand, 1142.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
The Cochrane database of systematic reviews
Periodical, Abbrev.
Cochrane Database Syst.Rev.
Pub Date Free Form
10-Apr
Volume
4
Issue
Start Page
CD006611
Other Pages
Notes
JID: 100909747; epublish
Place of Publication
England
ISSN/ISBN
1469-493X; 1361-6137
Accession Number
PMID: 27060875
Language
eng
SubFile
Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't; Review; IM
DOI
10.1002/14651858.CD006611.pub4 [doi]
Output Language
Unknown(0)
PMID
27060875
Abstract
BACKGROUND: Access to mobile phones continues to increase exponentially globally, outstripping access to fixed telephone lines, fixed computers and the Internet. Mobile phones are an appropriate and effective option for the delivery of smoking cessation support in some contexts. This review updates the evidence on the effectiveness of mobile phone-based smoking cessation interventions. OBJECTIVES: To determine whether mobile phone-based smoking cessation interventions increase smoking cessation in people who smoke and want to quit. SEARCH METHODS: For the most recent update, we searched the Cochrane Tobacco Addiction Group Specialised Register in April 2015. We also searched the UK Clinical Research Network Portfolio for current projects in the UK, and the ClinicalTrials.gov register for ongoing or recently completed studies. We searched through the reference lists of identified studies and attempted to contact the authors of ongoing studies. We applied no restrictions on language or publication date. SELECTION CRITERIA: We included randomised or quasi-randomised trials. Participants were smokers of any age who wanted to quit. Studies were those examining any type of mobile phone-based intervention for smoking cessation. This included any intervention aimed at mobile phone users, based around delivery via mobile phone, and using any functions or applications that can be used or sent via a mobile phone. DATA COLLECTION AND ANALYSIS: Review authors extracted information on risk of bias and methodological details using a standardised form. We considered participants who dropped out of the trials or were lost to follow-up to be smoking. We calculated risk ratios (RR) and 95% confidence intervals (CI) for each included study. Meta-analysis of the included studies used the Mantel-Haenszel fixed-effect method. Where meta-analysis was not possible, we presented a narrative summary and descriptive statistics. MAIN RESULTS: This updated search identified 12 studies with six-month smoking cessation outcomes, including seven studies completed since the previous review. The interventions were predominantly text messaging-based, although several paired text messaging with in-person visits or initial assessments. Two studies gave pre-paid mobile phones to low-income human immunodeficiency virus (HIV)-positive populations - one solely for phone counselling, the other also included text messaging. One study used text messages to link to video messages. Control programmes varied widely. Studies were pooled according to outcomes - some providing measures of continuous abstinence or repeated measures of point prevalence; others only providing 7-day point prevalence abstinence. All 12 studies pooled using their most rigorous 26-week measures of abstinence provided an RR of 1.67 (95% CI 1.46 to 1.90; I(2) = 59%). Six studies verified quitting biochemically at six months (RR 1.83; 95% CI 1.54 to 2.19). AUTHORS' CONCLUSIONS: The current evidence supports a beneficial impact of mobile phone-based smoking cessation interventions on six-month cessation outcomes. While all studies were good quality, the fact that those studies with biochemical verification of quitting status demonstrated an even higher chance of quitting further supports the positive findings. However, it should be noted that most included studies were of text message interventions in high-income countries with good tobacco control policies. Therefore, caution should be taken in generalising these results outside of this type of intervention and context.
Descriptors
Links
Book Title
Database
Publisher
Data Source
Authors
Whittaker,R., McRobbie,H., Bullen,C., Rodgers,A., Gu,Y.
Original/Translated Title
URL
Date of Electronic
20160410
PMCID
Editors
Potential harmful health effects of inhaling nicotine-free shisha-pen vapor: a chemical risk assessment of the main components propylene glycol and glycerol 2015 National Institute for Public Health and the Environment (RIVM), P.O. Box 1, 3720 BA Bilthoven, The Netherlands.; National Institute for Public Health and the Environment (RIVM), P.O. Box 1, 3720 BA Bilthoven, The Netherlands.; National Institute for Publ
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Tobacco induced diseases
Periodical, Abbrev.
Tob Induc Dis.
Pub Date Free Form
27-Jun
Volume
13
Issue
1
Start Page
15
Other Pages
015-0038-7. eCollection 2015
Notes
LR: 20150701; JID: 101201591; OID: NLM: PMC4482188; OTO: NOTNLM; 2015 [ecollection]; 2014/02/17 [received]; 2015/04/25 [accepted]; 2015/06/27 [epublish]; epublish
Place of Publication
England
ISSN/ISBN
2070-7266; 1617-9625
Accession Number
PMID: 26120296
Language
eng
SubFile
Journal Article
DOI
10.1186/s12971-015-0038-7 [doi]
Output Language
Unknown(0)
PMID
26120296
Abstract
BACKGROUND: A shisha-pen is an electronic cigarette variant that is advertised to mimic the taste of a water pipe, or shisha. The aim of this study was to assess the potential harmful health effects caused by inhaling the vapor of a nicotine-free shisha-pen. METHODS: Gas chromatography analysis was performed to determine the major components in shisha-pen vapor. Risk assessment was performed using puff volumes of e-cigarettes and "normal" cigarettes and a 1-puff scenario (one-time exposure). The concentrations that reached the airways and lungs after using a shisha-pen were calculated and compared to data from published toxicity studies. RESULTS: The main components in shisha-pen vapor are propylene glycol and glycerol (54%/46%). One puff (50 to 70 mL) results in exposure of propylene glycol and glycerol of 430 to 603 mg/m(3) and 348 to 495 mg/m(3), respectively. These exposure concentrations were higher than the points of departure for airway irritation based on a human study (propylene glycol, mean concentration of 309 mg/m(3)) and a rat study (glycerol, no-observed adverse effect level of 165 mg/m(3)). CONCLUSIONS: Already after one puff of the shisha-pen, the concentrations of propylene glycol and glycerol are sufficiently high to potentially cause irritation of the airways. New products such as the shisha-pen should be detected and risks should be assessed to inform regulatory actions aimed at limiting potential harm that may be caused to consumers and protecting young people to take up smoking.
Descriptors
Links
Book Title
Database
Publisher
Data Source
Authors
Kienhuis,A.S., Soeteman-Hernandez,L.G., Bos,P.M., Cremers,H.W., Klerx,W.N., Talhout,R.
Original/Translated Title
URL
Date of Electronic
20150627
PMCID
PMC4482188
Editors
Author's response to: "Harmful effects form one puff of shisha-pen vapor: methodological and interpretational problems in the risk assessment analysis" 2016 National Institute for Public Health and the Environment, Bilthoven, The Netherlands.; National Institute for Public Health and the Environment, Bilthoven, The Netherlands.; National Institute for Public Health and the Environment, Bilthoven, The Netherla
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Tobacco induced diseases
Periodical, Abbrev.
Tob Induc Dis.
Pub Date Free Form
7-Jul
Volume
14
Issue
Start Page
21
Other Pages
016-0087-6. eCollection 2016
Notes
LR: 20160710; JID: 101201591; OID: NLM: PMC4936250; 2016 [ecollection]; 2016/04/22 [received]; 2016/06/06 [accepted]; 2016/07/07 [epublish]; epublish
Place of Publication
England
ISSN/ISBN
2070-7266; 1617-9625
Accession Number
PMID: 27390574
Language
eng
SubFile
Journal Article
DOI
10.1186/s12971-016-0087-6 [doi]
Output Language
Unknown(0)
PMID
27390574
Abstract
Descriptors
Links
Book Title
Database
Publisher
Data Source
Authors
Bos,P.M., Kienhuis,A.S., Talhout,R.
Original/Translated Title
URL
Date of Electronic
20160707
PMCID
PMC4936250
Editors
Mobile phone-based interventions for smoking cessation 2012 National Institute forHealth Innovation, University of Auckland, Auckland,New Zealand. r.whittaker@nihi.auckland.ac.nz
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
The Cochrane database of systematic reviews
Periodical, Abbrev.
Cochrane Database Syst.Rev.
Pub Date Free Form
14-Nov
Volume
11
Issue
Start Page
CD006611
Other Pages
Notes
LR: 20160510; JID: 100909747; CIN: Evid Based Nurs. 2013 Oct;16(4):108-9. PMID: 23389384; UIN: Cochrane Database Syst Rev. 2016;4:CD006611. PMID: 27060875; epublish
Place of Publication
England
ISSN/ISBN
1469-493X; 1361-6137
Accession Number
PMID: 23152238
Language
eng
SubFile
Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't; Review; IM
DOI
10.1002/14651858.CD006611.pub3 [doi]
Output Language
Unknown(0)
PMID
23152238
Abstract
BACKGROUND: Innovative and effective smoking cessation interventions are required to appeal to those who are not accessing traditional cessation services. Mobile phones are widely used and are now well-integrated into the daily lives of many, particularly young adults. Mobile phones are a potential medium for the delivery of health programmes such as smoking cessation. OBJECTIVES: To determine whether mobile phone-based interventions are effective at helping people who smoke, to quit. SEARCH METHODS: For the most recent update, we searched the Cochrane Tobacco Addiction Group Specialised Register in May 2012. We also searched UK Clinical Research Network Portfolio for current projects in the UK and the ClinicalTrials register for on-going or recently completed studies. We searched through the reference lists of identified studies and attempted to contact the authors of ongoing studies, with no restrictions placed on language or publication date. SELECTION CRITERIA: We included randomized or quasi-randomized trials. Participants were smokers of any age who wanted to quit. Studies were those examining any type of mobile phone-based intervention. This included any intervention aimed at mobile phone users, based around delivery via mobile phone, and using any functions or applications that can be used or sent via a mobile phone. DATA COLLECTION AND ANALYSIS: Information on risk of bias and methodological details was extracted using a standardised form. Participants who dropped out of the trials or were lost to follow-up were considered to be smoking. We calculated risk ratios (RR) for each included study. Meta-analysis of the included studies was undertaken using the Mantel-Haenszel fixed-effect method. Where meta-analysis was not possible, summary and descriptive statistics are presented. MAIN RESULTS: Five studies with at least six month cessation outcomes were included in this review. Three studies involve a purely text messaging intervention that has been adapted over the course of these three studies for different populations and contexts. One study is a multi-arm study of a text messaging intervention and an internet QuitCoach separately and in combination. The final study involves a video messaging intervention delivered via the mobile phone. When all five studies were pooled, mobile phone interventions were shown to increase the long term quit rates compared with control programmes (RR 1.71, 95% CI 1.47 to 1.99, over 9000 participants), using a definition of abstinence of no smoking at six months since quit day but allowing up to three lapses or up to five cigarettes. Statistical heterogeneity was substantial as indicated by the I(2) statistic (I(2) = 79%), but as all included studies were similar in design, intervention and primary outcome measure, we have presented the meta-analysis in this review. AUTHORS' CONCLUSIONS: The current evidence shows a benefit of mobile phone-based smoking cessation interventions on long-term outcomes, though results were heterogenous with findings from three of five included studies crossing the line of no effect. The studies included were predominantly of text messaging interventions. More research is required into other forms of mobile phone-based interventions for smoking cessation, other contexts such as low income countries, and cost-effectiveness.
Descriptors
Links
Book Title
Database
Publisher
Data Source
Authors
Whittaker,R., McRobbie,H., Bullen,C., Borland,R., Rodgers,A., Gu,Y.
Original/Translated Title
URL
Date of Electronic
20121114
PMCID
Editors
Natural populations of lactic acid bacteria associated with silage fermentation as determined by phenotype, 16S ribosomal RNA and recA gene analysis 2011 National Institute of Livestock and Grassland Science, Nasushiobara 329-2793, Japan.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Systematic and applied microbiology
Periodical, Abbrev.
Syst.Appl.Microbiol.
Pub Date Free Form
May
Volume
34
Issue
3
Start Page
235
Other Pages
241
Notes
LR: 20151119; CI: Copyright (c) 2011; GENBANK/AB572027; GENBANK/AB572028; GENBANK/AB572029; GENBANK/AB572030; GENBANK/AB572031; GENBANK/AB572032; GENBANK/AB572033; GENBANK/AB572034; GENBANK/AB572035; GENBANK/AB572036; GENBANK/AB572037; GENBANK/AB572038; G
Place of Publication
Germany
ISSN/ISBN
1618-0984; 0723-2020
Accession Number
PMID: 21282025
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1016/j.syapm.2010.10.003 [doi]
Output Language
Unknown(0)
PMID
21282025
Abstract
One hundred and fifty-six strains isolated from corn (Zea mays L.), forage paddy rice (Oryza sativa L.), sorghum (Sorghum bicolor L.) and alfalfa (Medicago sativa L.) silages prepared on dairy farms were screened, of which 110 isolates were considered to be lactic acid bacteria (LAB) according to their Gram-positive and catalase-negative characteristics and, mainly, the lactic acid metabolic products. These isolates were divided into eight groups (A-H) based on the following properties: morphological and biochemical characteristics, gamma-aminobutyric acid production capacity, and 16S rRNA gene sequences. They were identified as Weissella cibaria (36.4%), Weissella confusa (9.1%), Leuconostoc citreum (5.3%), Leuconostoc lactis (4.9%), Leuconostoc pseudomesenteroides (8.0%), Lactococcus lactis subsp. lactis (4.5%), Lactobacillus paraplantarum (4.5%) and Lactobacillus plantarum (27.3%). W. cibaria and W. confusa were mainly present in corn silages, and L. plantarum was dominant on sorghum and forage paddy rice silages, while L. pseudomesenteroides, L. plantarum and L. paraplantarum were the dominant species in alfalfa silage. The corn, sorghum and forage paddy rice silages were well preserved with lower pH values and ammonia-N concentrations, but had higher lactic acid content, while the alfalfa silage had relatively poor quality with higher pH values and ammonia-N concentrations, and lower lactic acid content. The present study confirmed the diversity of LAB species inhabiting silages. It showed that the differing natural populations of LAB on these silages might influence fermentation quality. These results will enable future research on the relationship between LAB species and silage fermentation quality, and will enhance the screening of appropriate inoculants aimed at improving such quality.
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Elsevier GmbH
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Pang,H., Qin,G., Tan,Z., Li,Z., Wang,Y., Cai,Y.
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20110201
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