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1.
Article in English | MEDLINE | ID: mdl-38944417

ABSTRACT

While there is a large body of evidence indicating that sexual minority youth experience inequitably high rates of mental health problems (eg, depression, suicidality), we know little about how temporal changes in sexual attractions, identities and behaviour may impact mental health (and other) outcomes. In this essay, we review existing research regarding sexual fluidity and mental health among young adults in order to identify critical knowledge gaps with respect to an epidemiological understanding of the relationship between these factors. We describe three gaps that in turn inform a larger public health research agenda on this topic. First, there are a number of methodological challenges given that fluidity can occur over short or long periods of time and across multiple dimensions of sexual orientation (eg, attractions, identities and behaviour) with various patterns (eg, directionality of change). Tailored measures that accurately and inclusively reflect diversities of sexual fluidity trajectories are needed. Second, causal relationships between sexual fluidity and mental health remain uncertain and unquantified. Third, little is known about how features of context (eg, gender norms and political climate) influence youth experiences with sexual fluidity and mental health. Finally, we propose a set of recommendations to address these knowledge gaps to improve the quality of epidemiological research involving young people.

2.
J Adv Nurs ; 79(6): 2200-2210, 2023 Jun.
Article in English | MEDLINE | ID: mdl-36645111

ABSTRACT

AIM: To evaluate adoption, implementation and maintenance of the Queen's Nursing Institute Scotland development programme. DESIGN: A comprehensive, longitudinal, qualitative evaluation. METHOD: Participants from the first two cohorts were interviewed at different stages to explore adoption, implementation and maintenance. Managers of participants engaged in interviews to explore service changes. Facilitators took part in a focus group exploring delivery. A member-checking event was held. Data collection was between March 2017 and October 2019. Data analysis was thematically followed by the application of Normalization Process Theory. RESULT: Ninety-four interviews, two focus groups and a member-checking event were conducted. Prior to the programme most participants were burnt-out and considering leaving. Engaging led to a journey of self-discovery and transformation. The programme was perceived to change their way of thinking, personally and professionally, unlike any training and development previously experienced. Participants were rejuvenated and reinvigorated, sharing their learning with colleagues, service users and family, implementing new working practices and furthering their careers. They developed communities of practice amongst their cohorts with strong bonds; enabling them to build and sustain learnings. CONCLUSION: Participants experienced a journey of self-discovery and transformation unlike anything before due to the personal investment in them. Participants were rejuvenated and reinvigorated with many moving into new roles. The programme equipped them with a range of leadership and resilience skills. IMPACT: The Queen's Nursing Institute Scotland Development Programme had a profound impact on participants, personally and professionally, which was perceived as lifelong. These findings and programmes are transferable beyond Scotland and to different professions.


Subject(s)
Burnout, Professional , Learning , Humans , Focus Groups , Scotland , Leadership
4.
Emerg Med Australas ; 26(5): 510-1, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25145940

ABSTRACT

Current conventions for the writing of medical scientific papers impede clear communication of scientific research results. This article discusses the reasons for this and how to ameliorate them.


Subject(s)
Biomedical Research , Communication , Medical Writing/standards , Periodicals as Topic , Humans
5.
J Plant Physiol ; 168(8): 824-30, 2011 May 15.
Article in English | MEDLINE | ID: mdl-21134704

ABSTRACT

MicroRNAs (miRNAs) are a class of small non-coding RNAs that down-regulate gene expression in a sequence specific manner to control plant growth and development. The identification and characterization of miRNAs are critical steps in finding their target genes and elucidating their functions. The objective of the present study was to assess the genetic variation of miRNA genes through expression comparisons and miRNA-based AFLP marker analysis. Seven miRNAs were first selected for RT-PCR and four for quantitative RT-PCR analysis that showed considerably high or differential expression levels in early stages of boll development. Except for miR160a, differential gene expression of miR171, 390a, and 396a was detected in early developing bolls at one or more timepoints between two cultivated cotton cultivars, Pima Phy 76 (Gossypium barbadense) and Acala 1517-99 (Gossypium hirsutum). Our further work demonstrated that genetic diversity of miRNA genes can be assessed by miRNA-AFLP analysis using primers designed from 22 conserved miRNA genes in combination with AFLP primers. Homologous miRNA genes can be also identified and isolated for sequencing and confirmation using this homology-based genotyping approach. This strategy offers an alternative to isolating a full length of miRNA genes and their up-stream and down-stream sequences. The significance of the expression and sequence differences of miRNAs between cotton species or genotypes needs further studies.


Subject(s)
Amplified Fragment Length Polymorphism Analysis/methods , Gene Expression Regulation, Developmental , Gossypium/genetics , MicroRNAs/genetics , Polymorphism, Genetic , Base Sequence , Cloning, Molecular , DNA Primers/genetics , DNA, Plant/chemistry , DNA, Plant/genetics , Gene Expression Regulation, Plant , Genetic Markers/genetics , Gossypium/growth & development , MicroRNAs/analysis , Molecular Sequence Data , RNA, Plant/genetics , Random Allocation , Reverse Transcriptase Polymerase Chain Reaction , Sequence Analysis, DNA , Tetraploidy
6.
Dent Update ; 36(3): 146-50, 153, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19480102

ABSTRACT

UNLABELLED: Establishing the working length is an important step in endodontic treatment as inaccurate length determination may lead to failure. There is an ongoing debate regarding the extent of the apical limit of root canal preparation. This controversy is based upon different clinical opinions concerning the distance between the end point of the root canal preparation and the periodontal tissues. In this paper, we review the different schools of thought for working length determination, and how apex locators work and how they must be used for optimal accuracy. The reliability of these devices has been proven; the price is moderate and apex locators are now part of the basic armamentarium in the achievement of quality and predictable endodontic treatment. CLINICAL RELEVANCE: The technique of determining the working length from a single radiograph remains empirical, and apex locators should be considered an essential aid in establishing working length.


Subject(s)
Odontometry/instrumentation , Root Canal Preparation/instrumentation , Tooth Apex/anatomy & histology , Electric Impedance , Electrical Equipment and Supplies , Humans , Practice Patterns, Dentists' , Radiography , Root Canal Preparation/methods , Tooth Apex/diagnostic imaging
7.
Cochrane Database Syst Rev ; (4): CD003135, 2008 Oct 08.
Article in English | MEDLINE | ID: mdl-18843640

ABSTRACT

BACKGROUND: Inhaled fluticasone propionate (FP) is a relatively new inhaled corticosteroid for the treatment of asthma. OBJECTIVES: To assess efficacy and safety outcomes in studies that compared FP to placebo for treatment of chronic asthma. SEARCH STRATEGY: We searched the Cochrane Airways Group Specialised Register (January 2008), reference lists of articles, contacted trialists and searched abstracts of major respiratory society meetings (1997-2006). SELECTION CRITERIA: Randomised trials in children and adults comparing FP to placebo in the treatment of chronic asthma. Two reviewers independently assessed articles for inclusion and risk of bias. DATA COLLECTION AND ANALYSIS: Two review authors extracted data. Quantitative analyses were undertaken using Review Manager software. MAIN RESULTS: Eighty-six studies met the inclusion criteria, recruiting 16,160 participants. In non-oral steroid treated asthmatics with mild and moderate disease FP resulted in improvements from baseline compared with placebo across all dose ranges (100 to 1000 mcg/d) in FEV1 (between 0.1 to 0.43 litres); morning PEF (between 23 and 46 L/min); symptom scores (based on a standardised scale, between 0.44 and 0.7); reduction in rescue beta-2 agonist use (between 1 and 1.4 puffs/day). High dose FP increased the number of patients who could withdraw from prednisolone: FP 1000-1500 mcg/day Peto Odds Ratio 14.07 (95% CI 7.17 to 27.57). FP at all doses led to a greater likelihood of sore throat, hoarseness and oral Candidiasis. AUTHORS' CONCLUSIONS: Doses of FP in the range 100-1000 mcg/day are effective. In most patients with mild-moderate asthma improvements with low dose FP are only a little less than those associated with high doses when compared with placebo. High dose FP appears to have worthwhile oral-corticosteroid reducing properties. FP use is accompanied by an increased likelihood of oropharyngeal side effects.


Subject(s)
Androstadienes/administration & dosage , Anti-Asthmatic Agents/administration & dosage , Asthma/drug therapy , Administration, Inhalation , Adult , Child , Chronic Disease , Fluticasone , Humans , Placebos/therapeutic use , Randomized Controlled Trials as Topic
8.
Cochrane Database Syst Rev ; (4): CD003534, 2008 Oct 08.
Article in English | MEDLINE | ID: mdl-18843646

ABSTRACT

BACKGROUND: Inhaled fluticasone propionate (FP) is a high-potency inhaled corticosteroid used in the treatment of asthma. OBJECTIVES: 1. To assess the efficacy and safety outcomes of inhaled fluticasone at different nominal daily doses in the treatment of chronic asthma.2. To test for the presence of a dose-response effect. SEARCH STRATEGY: We searched the Cochrane Airways Group Trials Register (January 2008). SELECTION CRITERIA: Randomised trials in children and adults comparing fluticasone at different nominal daily doses in the treatment of chronic asthma. Two reviewers independently assessed articles for inclusion and methodological quality. DATA COLLECTION AND ANALYSIS: One review author extracted data. These were checked and verified by a second reviewer. Quantitative analyses where undertaken using Review Manager. MAIN RESULTS: Fifty-one published and unpublished trials (representing 55 group comparisons, 10,797 participants) met the inclusion criteria. In asthmatics with mild to moderate disease who were not on oral steroids, FP did not exhibit a dose-response effect in the lower dose comparisons in FEV1 (50mcg, 100mcg, 200mcg and 4-500mcg daily). There were no statisitically significant differences between 4-500mcg and 800-1000mcg, and between 50-100 and 800-1000mcg of FP. When 200mcg was compared with 800-1000mcg daily FEV1 favoured the four/five fold increase. For PEF, a dose response was present with FP when low and moderate, and low and high doses of FP were compared. There was no evidence of a dose-response effect on symptoms or rescue beta-2 agonist use. The likelihood of hoarseness and oral candidiasis was significantly greater for the higher doses (800 to 1000 microg/day). People with oral steroid-dependent asthma treated with FP (2000 microg/day) were significantly more likely to reduce oral prednisolone than those on 1000 to 1500 microg/day (Peto odds Ratio 2.8, 95% CI 1.3 to 6.3). The highest dose also allowed a significant reduction in daily oral prednisolone dose compared to 1000 to 1500 microg/day (WMD 2.0 mg/day, 95% CI 0.1 to 4.0 mg/day). AUTHORS' CONCLUSIONS: We have not found evidence of a pronounced dose response in FEV1 with increasing doses of fluticasone. The number of studies contributing to our primary outcomes was low. At dose ratios of 1:2, there are statistically significant differences in favour of the higher dose in morning peak flow across the low dose range. The clinical impact of these differences is open to interpretation. Patients with moderate disease achieve similar levels of asthma control on medium doses of fluticasone (400 to 500 microg/day) as they do on high doses (800 to 1000 microg/day). More work in severe asthma would help to confirm that doses of FP above 500 microg/day confer greater benefit in this subgroup than doses of around 200 microg/day. In oral corticosteroid-dependent asthmatics, reductions in prednisolone requirement may be gained with FP 2000 microg/day.


Subject(s)
Androstadienes/administration & dosage , Anti-Inflammatory Agents/administration & dosage , Asthma/drug therapy , Administration, Inhalation , Adult , Child , Chronic Disease , Fluticasone , Humans , Randomized Controlled Trials as Topic
9.
Dent Update ; 35(3): 172-4, 176, 178-9, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18507225

ABSTRACT

UNLABELLED: The fracture of an instrument is a recognized complication in endodontics. The immediate response to a fractured instrument is frequently to regard the treatment as a failure. Several factors must, however, be taken into account to evaluate the prognosis of the tooth in this situation. The objective of the endodontic treatment with or without a fractured instrument remains the same, namely to disinfect the root canal system and prevent its recontamination. The time at which file fracture occurred during treatment and the degree of canal infection should be considered when determining the potential effect of instrument fracture on treatment outcome. Patients must be informed about an instrument fracturing in their tooth for ethical and legal reasons. The aim of this paper is to attempt to place fractured instruments in context, not to provide an in depth description of fractured instrument management techniques. CLINICAL RELEVANCE: To understand the influence of fractured instruments on prognosis in endodontics.


Subject(s)
Equipment Failure , Root Canal Preparation/instrumentation , Root Canal Therapy , Dental Alloys/chemistry , Dental Pulp Cavity/drug effects , Dental Pulp Cavity/microbiology , Dental Pulp Diseases/microbiology , Dentist-Patient Relations/ethics , Equipment Design , Ethics, Dental , Foreign Bodies/therapy , Humans , Liability, Legal , Nickel/chemistry , Periapical Diseases/complications , Prognosis , Pulpectomy , Retreatment , Root Canal Irrigants/therapeutic use , Titanium/chemistry , Treatment Outcome , Truth Disclosure/ethics
10.
Emerg Med Australas ; 19(4): 383; author reply 383, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17655645
11.
Dent Update ; 33(9): 518-20, 522-4, 526-8, 530, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17176738

ABSTRACT

Root canal therapy is not always successful and an increasing number of patients are requesting retreatment to address intraradicular infection. The armamentarium available to assist the dentist, some of which is described in this article, has never been greater.


Subject(s)
Root Canal Therapy/instrumentation , Dental Pulp Cavity/anatomy & histology , Dental Pulp Cavity/microbiology , Gutta-Percha , Humans , Post and Core Technique , Retreatment/methods , Root Canal Filling Materials , Root Canal Obturation/instrumentation , Root Canal Obturation/methods , Root Canal Therapy/methods , Treatment Failure
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